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THE PHILIPPINE
JOURNAL OF SCIENCE
EDITED BY
PYNOIL, (Ch IRIDNOIS, Wil, IDS Ietat, 1D):
WITH THE COOPERATION OF
DEAN ©. WORCESTER, A. B.; MERTON L. MILLER, Pu. D.
LAWRENCE FE. GRIFFIN, Pu. D.; CHARLES S. BANKS, M. S.
_ ALVIN SEALE, A. B.; RICHARD C. McGREGOR, A. B.
NELLIE LOUISE COOK, B. L., M. A.
PUBLISHED BY
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VOLUME VI
1911
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CONTENTS.
No. 1, February, 1911.
Page.
I. Miller, Merton L. The Burial Mounds of Camiguin Island............ oi
Plates I to V.
ll. Bean, Robert Bennett, and Planta, Federico S. The Men of Cainta.. 7
Plate I.
III. Strohmeyer, H. Borkenkiifer der Philippinen.................2.002220-..-.... 17
Tafel I. Textfiguren 1 bis 8.
TY. Curl, Holton C. Notes on the Digestive System of Hydrocorax........ 31
Plates IT and Il. Text figure 1.
V. McGregor, Richard C. Notes on a Collection of Birds from North-
Gi INEEIOES! deo: ceneeeeeoatenlsteeseceretcen scar epee ewer heer nee -eneee see cace: aes. se Severecet 39
VI. Scheerer, Otto. On a Quinary Notation among the Ilongots of
TS (©THE GHEY DUELS a a se SecA REE ROR Se Be oe 4
WALES “TRENT ARE oc peer Bee See re eee pf cig sae deacoacocmneaoee HaSGOne RLENRCSNELSEREE 51
No. 2, April, 1911.
VIII. Douvillé, Henri. Les Foraminiféres dans le Tertiaire des Philip-
OPUS cel ee rn oe 53
Planches A aD. Figures dans le texte 1 a 9.
IX. Barton, Roy Franklin. The Harvest Feast of the Kiangan Ifugao. 81
Plates I to VIII.
X. Bean, Robert Bennett. Filipino Ears: III. Negrito.. 107
Plates A and I to XVII.
No. 3, June, 1911.
XI. Cole, Fay Cooper. The Bagobos of Davao Gulf... 127
Plates I to IV.
XII. Shufeldt, R. W. The Skeleton in the Flying Lemurs, Galeopteride.. 139
Plates A and I and II.
No. 4, August, 1911.
XIII. Worcester, Dean C. Newly Discovered Breeding Places of Philip-
ime Seay Bird Shes ce ee a accel cat sa teesteeee Rotate rattan te 167
Plates I to VIII. i
SV. Worcester, Dean C. Hybridism among Boobies...................-------------- 179
Plate I.
XV. McGregor, Richard C. Record of a Pufiinus New to Philippine
Waters and Description of a New Species of Micranous...............-..- 183
XVI. Shufeldt, R. W. The Skeleton in the Flying Lemurs, Galeopteride.. 185
Plates III to V.
XVII. Pearse, A. S. On the Habits of Thalassina anomala (Herbst)... 213
Plate I. Text figures 1 and 2.
XVIII. Pearse, A. S. Concerning the Development of Frog Tadpoles in Sea
Water
XIX. Reviews
IV
XXI.
XXID-
XXIII.
XXIV.
XXV.
XXVI.
XXVII.
CONTENTS.
No. 5, November, 1911.
. Beyer, H. Otley, and Barton, Roy Franklin. An Ifugao Burial
Gerri niyo 22 ck are eee ees eae aaa ca asm aoe
Plates I to X.
Griffin, Lawrence Edmonds. ‘ A Check-List and Key of Philippine
Snakes —........... aN E SPe ec 3c SPR...) 3s Le eat te ee
Text figures 1 and 2. ;
TRGVil GW aeeers eres tS 7 ee ee enc = Seve
No. 6, December, 1911.
Seale, Alvin. The Fishery Resources of the Philippine Islands,
Part IV, Miscellaneous Marine Products..............-....2.-2.2----2------2-0---
Plates I to XII.
Miller, Merton L. The Non-Christian People of Ambos Camarines..
Plates I to IV.
Griffin, Lawrence E. The Structure of the Pallial Tentacles of
Lima Species Ee eS
Text figures 1 to 4.
Moser, J. Beitrag zur Coleopteren Fauna der Philippinen............
U6 (Sy: Pine eee ee ae eee ee eae or ee MES 2 2
‘Vou. VI FEBRUARY, 1911 No. 1
THE PHILIPPINE
JOURNAL OF SCIENCE
EDITED BY
PAUL C. FREER, M. D., Pu. D.
WITH THE COOPERATION OF |
DEAN C. WORCESTER, A. B.; MERTON L. MILLER, Pu. D.
LAWRENCE E. GRIFFIN, Pu. D.; CHARLES S. BANKS, M. S:
ALVIN SEALE, A. B.; RICHARD C. McGREGOR, A. B..
“NELLIE LOUISE COOK, B. L., M. A.
PUBLISHED BY
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STUDIES IN MORO HISTORY, aa AND RELIGION.
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107 pages. 16 illustrations. 5 diagrams.
A treatise on ine history and customs of the Moro People.
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THE HISTORY OF SULU. , tf
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ME FEBRUARY, 1911 No. 1
THE BURIAL MOUNDS OF CAMIGUIN ISLAND.
By Merton L. Mixxer.
_ (From the Division of Ethnology, Bureau of Science, Manila, P. T.)
Island of Camiguin lies north of the northern end of Luzon, about
meters distant from Aparri. It is approximately 20 kilometers in
e length and 12 kilometers in extreme width.
the time of my arrival on the island, April 17, 1910, there was a
ulation of 90 souls. During my stay of six weeks 30 people arrived
from Dalupiri and other neighboring islands with the intention of remain-
ing on Camiguin. Tradition says that there was formerly on the island
a population of several thousand, but that the greater part of the people
d of cholera between twenty and thirty years ago.
Camiguin is almost entirely covered with forests. If there formerly
a numerous population on it, the clearings which would have been
de have hecome reforested, unless there is some open country of which
ivee individuals who have come from the Batanes Islands. Some
ocanos were born on Camiguin and some came from the [locos
from the Cagayan Valley. I can not say what the pro-
f native born to immigrants. All the people live within a
9 MILLER.
valley to the south of Cadadalman, but the majority are at Malatubat, a
comparatively large valley which opens out on the other side of a rocky
point, north of Cadadalman.
The extinct voleano, known to the natives as Dakelabalai, rises at the
extreme southeastern point of Camiguin. There are several places with
an area of from 10 to 20 hectares on the southwestern slope of this moun-
tain where there is no vegetation and where there are many openings in
the ground which emit sulphurous fumes. On these bare places and on
grassy spots just beyond them are numerous artificial heaps of ‘stones.
Captain Mitchell, of the Signal Corps of the United States Army, was
on Camiguin in the latter part of 1909. He was much interested in
these stone piles and opened two or three of them. In the center of each
he found a large earthenware jar.
My visit to Camiguin was for the purpose of discovering some clue to
the people who buried these jars. The stone piles were found to be’ from
15 to 3 meters in diameter and were made up of stones ranging in size
from a few centimeters to 50 centimeters in diameter. The mounds
rose from 50 to 80 centimeters above the general surface of the ground.
The stones in some cases covered a mound of loose, brown earth mixed
with loose stones, in others, a mixture of sulphur and clay, either in the
form of a powder, or consolidated into rock, probably by the deposition of
sulphur. In the center of each was an earthenware jar. The greater
number of these jars were broken, usually so badly that they could not
be taken out. The earth im which many of them were embedded was
moist and the jars, which appeared to have been poorly baked, were in
consequence easily destroyed. ‘They hardened on drying in the air.
Those which were embedded im the hardened sulphurous mass in some
cases were broken, in others they could not be removed without breaking,
while in a few instances it was possible to get them out. A few jars had
an inner coating of very delicate crystals of sulphur.
The vessels varied in size from 20 to 60 centimeters in diameter, and
in height from 20 to 80 centimeters. Some of them had mouths but
little narrower than the greatest width of the jar, while others had small
openings, not more than 15 centimeters in diameter. All had originally
a ‘cover of some kind over the opening, either an inverted jar or a true
cover. Only in the case of one small vessel did I find the cover unbroken,
so that I could determine its form. This cover was of almost the same
shape as the jar below. ‘The fragments which I found led me to infer that
some of the covers had extended about halfway down the side of the body
of the jar, being in reality inverted jars; others seemed to have covered
the opening of the vessel and to haye extended but a short distance beyond
the edges.
-There can be no doubt that these jars were used for containing the
bones of the dead. The merest fragments of bones were found in two
BURIAL MOUNDS OF CAMIGUIN ISLAND. 3
of them, but they were too small to determine what bones they were; a
third jar contained a small piece of one of the bones of the skull. In one
of the jars were found a few common, pale blue, glass beads together
with a piece of dark brown, loosely woven, coarse fabric, which fell to
pieces at a touch of the hand. In another jar a few more blue beads of
the same kind were seen together with a black, sticky mass which had a
yery unpleasant odor.
I found it almost impossible to secure any information on the island
about the customs of former times, because the people native to Camiguin
had all died and the few old people still living had come over from Luzon
or from other islands in recent years. he only statement as to the use
of these jars which I could secure was from a young man who told me
that he had heard an old man say that they formerly buried the dead in
earthenware vessels, cutting the legs of the corpse at the kmees so as to
make it possible, by doubling the legs, to put the entire body into a jar.
While this may have been one practice followed, it could not have been the
only method of burial, because many of the jars had openings too small to
admit the body even of a young child. Of course, it is possible that two
methods of burial might have been followed at the same time, one, that
of putting the dead body in a jar, and the other, that of placing the bones
only in the vessel after the flesh had either been removed or allowed to
decay. The presence of the black, sticky mass and the beads in one jar
and of the piece of fabric and beads in another would seem to argue for
the first method, and the small openings in many of the jars are certainly
an argument for the second method.
I made inquiries of many people as to the existence of similar heaps of
stones in other parts of the island, but I could learn of none excepting a
few on the other side—northeast—of the volcano from those already de-
scribed. These I visited and examined. They were found to be of the
- same general style as those to the southwest of the volcano. I was told
that at the extreme northern end of the island similar mounds were to be
found. However, when I arrived there the guide pointed out certain
heaps of stones which on examination proved to be natural outcrops of
rock. I believe from what I learned after leaving Camiguin that possibly
there are other burial mounds on the island besides those which I saw.
J do not see that there is any reason for concluding that these burials
were made by any other people than Filipinos who formerly inhabited
Camiguin. Cave burials have been found on at least one island off the
northeast coast of Surigao, and others have recently been reported from
the Island of Bohol. Burial jars containing bones have also been found
in the vicinity of Dapitan, Mindanao.
However, perhaps the most interesting fact in this connection is that
I was told that jars similar to these on Camiguin are to be found on
Calayan, an island northwest of Camiguin. An old woman who has
4 : MILLER.
lived on Camiguin for the past five years told me that formerly she lived
on Calayan and that jars like those found on Camiguin were also found
buried on the latter island, but she did not know what purpose they had
served nor why they had been buried.
Tt is to be hoped that some day evidence will be found which will give
a clue to the time when the dead in the Philippines were buried in jars
and in caves.
ILLUSTRATIONS.
Prare J. Dakelabalai Mountain with burial sites in the foreground.
IJ. Burial mounds near sulphur fumaroles.
III. Burial mound.
TV. Burial mound.
V. Fig. 1. Partly excavated jar buried in a mixture of clay and sulphur.
2. Partly excavated jar buried in a mixture of clay and sulphur.
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MILLER: BURIAL MOUNDS OF CAMIGUIN ISLAND.] [PHIL. JOURN. Scr., Vou. VI, No. 1.
PLATE v.
THe PHILIPPINE JOURNAL OF SCIENCE,
D. General Biology, Ethnology and Anthropology.
Vol. VI, No, 1, February, 1911.
THE MEN OF CAINTA.
By Roserr Bennerr Bean and Freperico 8. PLANnra.
(Prom the Anatomical Laboratory, Philippine Medical School, Manila, P. I.)
The town of Cainta, a stone’s throw from Taytay near the Lake of
Bay (Laguna de Bay), is of considerable historic interest because of the
many bloody battles fought in its vicinity between the Spaniards and
the natives, the Chinese and the natives, and the Spaniards and. the
Chinese. It is of great interest to the anthropologist because it presents
a body of people different from. the surrounding population.
Cainta was founded before the Spaniards came to the Islands, according to a
statement in a history of the Philippines by Jose Montero y Vidal, who, in the
first volume, page 41, affirms that Capitan Juan Salcedo, one of the first
Spanish conquerors who came to the Philippines, having in 1571 subdued the
natives of Cainta and Taytay first, went to the Lake (La Laguna), pacifying
many towns.
There seem to be no data concerning the origin of the inhabitants of Cainta,
but one of two suppositions is plausible. Hither they are derived from settlers
of East Indian origin who arrived before the Spaniards, or else they represent
the descendants of a British regiment of Hast Indian troops who remained
when the British evacuated the Philippines in 1763. The history of P. Murillo,
written in 1752, volume 7, page 33, speaks of some of the inhabitants of the
Philippines, when the Spaniards arrived, as black people, called for politeness’
sake Creoles (Qriollas or Morenos), who were characterized as very active
politically. Murillo believed that these people came from Malabar or Coro-
mandel, belonging to the British, and they were probably of East Indian origin.
P. Juan de Salcedo, in his history, page 264, speaking of those Morenos or
Criollas, says that they have long, straight hair, long noses, and wide open eyes.
He speaks further of some similar people from Malabar that he had known in
Manila, who married and settled nearby in Santo Tomas and at times came to
Manila on business. He also says that if they were not known as natives of
the Philippines they might be regarded as Huropeans, except for their dark
skins. .
P. Martinez asserts in his Estadimos de Filipinas, page 264, that at the
beginning of the conquest of the Philippine Islands by the Spaniards there
came Moors from Hindustan trading with the natives.
From these statements one may infer that the people of Cainta are
of East Indian origin and occupied the town before the arrival of the
Spaniards. Current opinion among Filipinos differs in regard to this,
although many reliable Filipinos inform me that tradition states their
7
5 BEAN AND PLANTA,
origin in a different way. A company of Hast Indian soldiers, stationed
at Cainta during the British occupation of Manila, was overlooked when
the British embarked and they settled and remained there.
It seems to me that both suppositions may be true. The town of
Cainta was originally settled by East Indians, and a few men from
among the British troops of East Indian origin remained when the
British evacuated Manila.
The inhabitants of Cainta impressed me as being tall, black-skinned,
long-nosed, and open-eyed in contrast with the inhabitants of Taytay
who are small, brown-skinned, short-nosed, and not open-eyed. Some of
the men I saw in Cainta were more than 180 centimeters in height,
and the skin of many was of so dark a brown as to appear black. The
face is large and long and the nose is notably high and long, the eyes
large, with wide open lids that give the peculiarly attractive expression
to the countenance which is often seen among Hast Indians. Whatever
may have been the proximate origin of the people, I believe there can be
no doubt as to their Indian origin ultimately.
In any event, they probably settled in Cainta and married Filipinos.
Their descendants then Tesemble both Indians and Filipinos, with
probably a preponderance of the former; at least such is the appearance
by casual observation, and such is the actual condition as determined by
measurements.
The measurements of 38 men of Cainta give average dimensions that
are in almost every part slightly different from similar dimensions of
the men of Taytay, and the differences are invariably in the direction of
the Huropean. The average differences are slight, as may be seen by the
accompanying list, but they are significant because they are averages and
because all the differences simulate the European.
TABLE I.—Average dimensions—physical characters of adult males at Cainta,
greater or less than men of Taytay.
¥ l |
Character. eee Character. | een |
| apr pees ee :
| Body: | Head:
Statnre wesce bond Seela i neele ee 1.43 || Maximum length____ +0. 10 |
Sith Sebel shi ee nee —0.39 Maximum breadth _________-_____ —0. 26
Pupicheisht ee see eae —2. 32 Maximum height.-_______________ +0.13
Umbilical height —----_. -----_-- = —1.1d Minimal frontal breadth _________ —0.04 —
Sternslybeis hte ee —1.82 Bizygomatic breadth _____________ | =o!37 |
Chinvheight === =e ene —1.33 Bimastoid breadth________________ Soil |
Warhei gh teense -aee ee eee —1.00 Bigoniac breadth _________________ —0.19
Amide whei shtassse ses a se ene —0.18 Naso-buccal distance -____________ | —0.05
Knee height_____ ee ee a ste —0. 89 Naso-alveolar distance +0. 03
Trochanter height a — 2.42 Nose height (base) - +0.04 |
Fingertip height____--_-__--_-___ —0. 26 NOSE IbTes Cb hice es teens —0.10
“Wristpheizht=2====- = hese 3s —0. 65 Nose length____________ | +0.09
bo wale) gies —1.71 Chin nasion distance __ +0.30 |
Acromion height _---------_-_-_- | —2.51 Nasion hair line distanee_________ —0.36 |
THE MEN OF CAINTA, 9
Taste 1—Average dimensions—physical characters of adult males at Cainta,
greater or less than men of T'aytay—Continued.
| Character. | Gen | Character. cent |
Head—Continued. || Head—Continued. \
Mouth breadth (lips) ~------..---- +0.15 | Eye length (transverse) -___---__- 0.07
Mouth lex tho 25 soo ee eet +-0.10 | Frontal cireumference____________ |
) OF 0) 5206 Us —0. 01 Parietal circumference |
Ear length —0. 05 Forehead circumference |
Ear cartilage length | +0.14 | Occipital cireumference__.__----_| —0.38
Interocular distance---..--------.| —0.08 |
It is to be reckoned that the indices and relative factors will also
differ between the two groups of men because the actual measurements
are different, and such is the case, as may be seen by the following list,
all pointing to the European origin of the Cainta Indians.
TABLE 11.—WMen of Cainta, indices, and relative factors, greater or less than men
of Taytay.
Factors. | a | Factors. | ent |
j Sn #: jes =| 2 | |
| Indices: | Relative lengths: |
—2. 75 \ Lower lege-22=20-— =-Ae See ees } 0.23
—2. 40 | Upperleg seo 2 ee aaa hae +0. 60
COED NO 2. = ee ee et a —1.39 || a 0 eee ee | +0.05
Physiognomie ___-_______-__.___- —0.20 Worearm’ = 230222 Sehr eee | +0.65
1 Morpholopie == == == 5-8 422 24) | +-4.40 H Upper arn eee | ==01s01,||
Wmmbeeractiaiees. A280 oe es | +3.80 | |
In only one index, the brachial, does the Cainta Indian resemble
other people than the European, and this index is like that of the Negro.
It is also the most distinctive characteristic of the body parts of the
Negro. There is then evidence of Negro mixture in the Cainta Indians,
more than in the Filipinos of Taytay.
The individuals, more than the average, show distinctive European
markings. One indication of European extraction for the Cainta men is
the presence of a relatively large number of Iberians, more than one-
third of the total number measured. The Iberians of Cainta also appear
to be purer than the Iberians of other parts of the Philippines. Take
for instance No. 15 with a stature of 163.6 centimeters, nasal index 77.7,
cephalic index 75.9, and omphalic index 35.9, almost a typical Iberian.
The face is long and narrow, the body is short, and the legs are long,
all Iberian characteristics. Notice may also be taken of the three men
in the plate accompanying this article. who represent Iberians of type
B in figure 1, type A in figure 2, and type C in figure 3. Front and
10
BEAN AND PLANTA.
Tasre I1I.—Afen
Type of
individual. }
be eee
Alpine
Australoid== = esl
fiers eed
TRUS, — 2-2 sees |
200 eS
Australoid-=== => Ss)
ibeian et
Blend bse Se a
Se =
Ausiaoids= =
Australoid__
Bic eee
Bsiend
Blend ==
Australoid- 2 ==
Blend ee
(AUSiTal oid ==
Bie eet
Blend = SSS ed
ites —— ee
ipenaD =e
-S e—eE—E———eee
AD 6 eee
Tbetian 2
General average ___________
3
=
E
a
a
=
2
g
1
2
| 3| 371 | 176.3 | $9.2
4
5
6
7
8
9
10
u
2
13
SOERSERESBERES
bh
or SI
Body.
| Clinical number,
Sitting height.
Stature
Pubie height,
Umbilical height,
Sternal height.
Chin height.
Trochanter height.
Pinger tip.
Ankle height,
Knee height,
Har height.
Wrist height.
Elbow height.
Acromial height.
|
159.0 } $5.3
150.5 | 81.4
479 | 157.3 | 84.3
____-| 148.1 | 80.9
{eae 161.0 | 84.7
|__| 161.5 | 83.0 |
| 161.0 | $0.0 |
| 160.0 | 86.0
| aren | 166.0 | $4.5
169.4 | $5.0
|_____| 154.0 | 82.0
| 87.4
| 164.0 | 86.5
14 |_____| 169.0 84.3 |
| 15 |---| 163.6 | 81.0
| 16 |__| 166.0 | 86.6 |
| 167.0 | $5.0 |
161.2 | 76.3 |
157.0 | 81.6 |
| 158.5 | $3.2 |
(162.5 | 76.0
158.0 | 84.0 |
155.5 | 83.0)
157.0 | $3.0)
25 |_____| 160.0 | $3.0
(2) | 83.0}
161.0| $1.0
| 155.0 | $4.0)
| 159.0 | 84.0
166.5 | 87.5 |
| 151.6 | $2.0
162.0 | 86.5 |
| 163.5 | $5.5
34 |__| 164.8 | 86.0
35 |__| 169.0 | 85.5 |
Ay Lo 161.5 | 84.8 |
37 |---| 159.0 | 82.7 |
38 |__| 160.0 | 86.8}
ab) oa 160.9 | 83.6 |
|
|
|
80.0
76.5
5.2
80.6
74.0
82.6
§3.6| 98.5
87.5 | 105.0
81.0| 97.0
101.3
143.3
124.8 | 133.0
86.3 | 119.0 | 123.5
131.0 | 137.0
133.0 | 138.0
130.3 | 134.5
134.0 142.0
91.0 | 104.0 139.0 | 145.5
95.0) 93.0 | 126.0 | 131.0
$4.5 StA8 THAAD 141.0
89.0 104.0 | 140.0 | 148.0
87.0| 99.7 | 135.0 | 141.6
$5.0 | 100.0 | 137.0 | 144.5
$8.0 | 102.5 | 137.0 | 143.3
85.0} 99.5 130.3 | 139.0
/
$0.8} 92.5 | 128.2 | 134.3
78.5 | 93.3 | 128.6 | 135.7
81.0) 92.6 | 123.0 | 198.5
79.0 | 93.0 | 128.0 | 132.0
$1.5| 92.0 | 124.5 | 134.0
$2.0 95.0 | 126.0 | 135.0
84.0| 97.0 | 129.0 133.0
77.0| 94.5 126.0 | 133.0
$4.0} 96.0 | 133.0 | 137.0
79.0 | 92.0 125.5 | 132.0
81.0) 958 127.0 | 188.7
$9.0 | 104.0 135.6 | 142.3
79.0 | 89.0 | 124.0 | 128.0
$2.5] 95.0 | 131.0 | 141.0
$6.6 | 99.5 133.0 | 140.6
$6.0 | 100.0 | 135.0 | 142-0
91.0 | 101.0 | 139.5 | 144.0
$2.6 | 97.4 | 131.5 | 136.8
$6.2| 96.0 129.0 | 135.5
$9.5 | 104.0 | 138.0 | 145.5
$4.1)
(E82 bg | 137.6
|
91.0 | 129.8 | 137.8
86.7 | 118.5 | 126.7 |
149.7 |
136.6 | 7.7 | 42.0 | 74.5 | 56.3
96.3 | 130.3 } 138.7
159.0 | 7.3
|
73.7
72.5
146.8 | 7.8
| 43.5 | 81.6 | 57.5
160.1 | 7.4 | 50.2 | 96.4 | 59.8
142.8 | 5.8 | 41.0) 81.6 | 54.4
134.5 | 6.0 | 39.2 | 73.0 | 58.0
148.9 | 7.0 | 45.2 | 84.1 | 56.0
145.0 | 7.0 | 45.5}
|
157.0 | 7.1 | 48.7
139.0 | 6.3 | 42.5 | $0.0 | 58.0 | 76.0
152.0 | 7.8 | 43.7 | 85.4 | 59.0 | 75.5 |
156.0 | 6.8 | 47.5 | 91.0 | 60.0 | 79.0)
151.5 | 7.1 | 44.3 | 91.0 | 59.0
152.8 | 7.2 | 44.0 | 87.3 | 58.8
158.6 | 7.5 | 45.0 | 93.0 | 61.0 | 79.5
149.0 | 5.6 | 45.2 | $6.0 | 56.6 74.0)
145.2|6 59.0 76.0
145.5 | 6.4 | 45.1| 88.7) 54.5 | 72.2
136.5 | 6.2 | 42.5 | $2.0 | 49.5
144.0 | 6.2 | 42.0 | $3.0 | 55.0 | 73.0
142.0 | 6.0 | 43.0 80.5 | 51.5 | 68.8)
144.0 | 4.8 | 44.0 | 82.0 | 53.0/ 73.0 |
145.0 | 6.8 | 46.0 | 87.0 | 62.0 | 79.0
142.0 | 5.8 | 40.0 | 80.5 | 56.0 | 74.0
147.0 | 6.0 | 43.0 | 86.5 | 59.4 | 7.2 |
142.0 | 5.8 | 44.0 | $2.0 | 55.0 | 73.0
145.5 | 6.8 | 45.0 | $1.2
152.6 | 6.8 | 46.5 | 90.0 | 58.0
140.0 | 8.7 | 42.0) 82.0
149.3 | 6.2 | 43.6 | 36.0 |
151.6 | 7.2 | 47.0 | $7.6
152.5 | 7.1 | 47.0 | 89.0
155.8.| 8.3 | 48.5 | 94.0
147.0 | 6.5 | 42.4
146.0/ 6.8 48.5 87.0
90.8 | 60.6 | 79.7
gt
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93.7 | 123.5
79.8 | 106.8 | 142.8 |
72.0) 95.6 | 128.2)
69.8 89.5
73.3: 97.6
147.7 | 6.5 | 44.5 | 85.0 | 56.5 | 75.0/ 100.0 132.5)
148.0 | 6.4 | 47.0 | 88.0 | 59.8 | 77.0 102.0
84.5 | 55.0 73.0) 99.0
152.0 | 6.8 | 46.6 | 89.0 | 58.0 | 77.0 | 104.0
131.0 |
99.0 | 135.0
103.0 | 135.2
| 136.6
92.0 | 124.5).
96.0 | 129.5
92.0 | 124.0
96.0 | 128.8
102.0 | 130.0
97.5 | 129.0
75.0 | 99.0
76.0 | 103.5
72.7| 95.0
5.0| 99.0 131.0
7.0 | 102.0 | 135.5
9.0 | 104.0 | 138.0
$1.0 | 106.5 | 140.0
78.6 | 102.0 | 133.2
75.0 | 101.3 | 132.0
| 78.1 | 105.0 | 140.6 |
147.1 | 6.7 | 44.7 | 85.5 | 57.3
t u i 1
120.6
135.0,
130.0 |
135.4 |
140.6
127.0
139.9
139.4
131.8
131.0
131.0
133.0
323.8
129.5
138.2
124.5
753 | 99.4 | 132.1 |
he
THE MEN OF CAINTA. 11
of Cainta, Rizal.
= —' oe ny
Head. 5 |
9 | ¥ Py alse ieee |
aHBE EL EEE LE |
elel|2|s ls Sole ae I SEE BEI
Bes} a lets |. tied) eed eb dee ese eel al eal he S8lsslos/35s| &
Meese sls leislsl2islflelslBleleleiSls] Sis is8|_2]s8la3| 3
5 |} 3 Siseis)|/4)4 al/e/8)/F lala | M/S] Bl Slay sls?) S
MHI SIS IS ale le lalFl2lslFlFlslalale/8l3)sisia 12 18 le | 8!
BERGeeees bein he lS|si(elel ae iele/slelrlelSisiele le le ls |e |
Pee Sais (Milind | as iio lal a jo lo} of oO) a | Sie Sle ia |e |e 1s 8
VS (S/S )/8/S |B 1B lala l42)4)o/4)|4/ 4 Ala l|al|al ae lala je ja jo Q
| Ta aa = a a eesasl pease (i 3
148.0 | 14.2 | 12.5} 10.7] 18.0 | 12.5 | 10.6 | 7.0 | 6.3 | 3.0/ 6.3 | 11.5 | 3.6} 4.7] 2.2 | 5.1) 8.4| 5.6) 3.0] 6.2 | 1.5 | 30.0] 35.0 | 26.0| 29.6 | 4.5
17.5 | 14.8 | 12.0 | 10.4 | 18.6 | 12.3 | 10.9| 6.9 | 6.7 | 2.7| 6.4 | 11.5] 3.7) 5.1] 1.8 | 4.9|3.8|5.6| 3.4) 5.7 | 2.5] 31.8] 84.2] 27.7] 27.6) 4.5
148.4} 14.7 | 13.2 | 20.2 | 18.6 | 13,5 | 11.0] 7.4] 6.5) 3.2| 7.0| 12.2| 4.2/5.0] 2.6 |4.3|3.8|6.4| 3.4] 6.8 | 8.0/ 32.3] 36.2] 27.0| 29.5 5.4
18.3 | 14.9] 12.2} 9.9] 14.3 | 13.0 | 11.4] 7.7] 6.3 | 3.1] 7.5| 10.7] 3.7) 4.8] 1.7 | 4.7/3.6 | 6.4| 3.1] 5.9 | 2.0| 30.4] 34.8 | 27.8 28.0 5.5
1} 18.1 | 15.0} 12.8 | 10.8 | 14.2 | 18.1] 11.0] 7.6 | 6.5 | 3.2 | 8.5) 11.7 | 4.5] 5.0| 1.0 | 5.0] 4.0/ 7.8|3.3] 6.4 |3.0| 80.6 | 35.8 | 28.0) 28.7| 5.9
18.5 | 14.6 | 12.8 | 10.8 | 18.8 | 13.3 | 10.8| 7.4] 7.0} 2.7| 6.8 | 11.8] 4.1/4.8] 1.5 | 5.1/3.5] 6.0| 3.6] 6.5 | 3.0| 28.8 | 35.3 | 27.8 | 28.2) 4.6
+} 18.2 | 15.4} 13.3 | 10.0 | 12.8 | 12.6 | 10.4] 7.4| 7.2) 3.5/6.0 | 12.0/3.5) 5.3] 2.5 | 4.8|3.7| 5.9/3.1] 6.2 | 5.0] 31.0! 36.5 27.0 | 27.0) 5.3
418.0 | 15.2 | 11.8 | 11.5 | 14.0 | 12.8 | 11.3] 7.2] 6.4 | 3.0} 7.2] 21.2] 4.0/4.6] 2.1 | 4.6/3.7) 6.9] 3.6| 6.4 | 2.0| 30.8 | 35.3] 28.4 | 27.5) 5.3
1} 17.8 | 14.9 } 18.0 | 10.0 | 13.0 | 12.8 | 10.2 | 7.3| 6.8 | 2.9| 6.0|12.0}4.2 | 5.1| 2.3 | 5.0/3.6 | 6.3] 3.0] 6.0 | 3.0] 31.0 | 37.0} 26.5! 26.5 | 5.4
19.3 | 15.0 | 12.9 | 10.7 | 14.5 | 13.0 11.0] 6.8 | 6.6 | 3.0| 7.0 | 11.2) 4.8) 4.7| 2.5 | 5.4) 8.7) 6.7/3.7] 6.4 | 4.0| 31.7 | 36.0 | 28.8 | 28.8) 5.4
| 18.6 | 14.5 | 11.7 | 10.1| 18.6 | 13.0 | 11.3] 6.8 | 6.5 | 3.3 | 8.0| 11.8/4.0| 4.9) 2.1 | 5.2 3.8 | 6.2| 3.2] 6.5 | 5.0| 29.0| 33.0] 26.0} 28.5 | 5.2 |
1} 77.6 | 14.2}12.2} 9.6] 12.2| 12.0] 10.5| 6.5] 5.7} 2.2| 5.8 | 10.5 | 3.8) 4.2} 2.1 | 4.8/3.5] 6.2] 3.3| 5.9 | 3.0| 30.0] 34.8 | 26.2 | 27.0| 5.2
1) 18.2 | 14.6 | 12.5 | 10.4 | 13.2 | 12.6 | 10.5 | 6.6} 6.1| 3.2| 6.0} 11.3| 3.8/4.7) 2.3 | 5.0} 3.3/5.6) 3.1| 5.9 | 1.0| 30.5 | 35.8 | 28.3 | 26.4) 4.8
17.6 | 15.4] 12.0) 9.7} 12.9} 18.4 | 10.1| 7.2 | 6.6 | 3.1] 7.0} 11.0] 4.2/5.0] 2.7 |5.3| 3.4] 5.6] 3.0] 6.0 | 3.0|____|-____ [eae ieee ea te
48.7 | 14.2 | 12.0| 10.2/12.7/12.2| 9.7/7.1) 6.6/2.8] 7.3) 11.5|3.5/4.5| 1.9|4.5|/3.9/ 6.0/3.2] 5.7 | 3.5| 28.5) 35.4 25.7] 29.6| 5.4 |
18.7 | 14.1| 12.3 / 10.7 | 18.9 | 12.5| 10.2] 6.6 | 6.1| 2.8) 7.7|11.3|8.8| 4.4] 1.8 | 4.3) 3.9|6.5| 3.5] 6.1 | 1.0} 29.9 | 32.5 | 28 0) 27.8 | 5.5
18.8 | 15,1| 18.5 | 11.1) 14.1] 12.6 | 10.1] 6.7 | 5.8 | 3.5 | 6.4 11.0/ 4.0 4.5) 2.0 | 5.1/8.1) 6.0/8.7) 6.1 | 3.5 | 82.5) 87.0) 28.5 | 25.7 | 5.1
48.3 | 13.5 | 12.5 | 10.2 | 12.8 | 12.3 | 10.4| 7.2 | 6.3 | .1| 7.7] 11.6 | 4.4 | 4.7] 1.6 | 4.8 | 4.0/6.9] 3.2] 6.1 | 3.0 | 30.8 | 34.2 | 27.0} 26.4 | Fi |
18.7 | 14.4 | 12.4 | 10.0 | 13.2 | 13.3 | 10.2 | 7.9 | 7.0 | 3.6 | 7.4 | 12.1 | 4.0) 5.4| 1.6 | 5.5 | 3.9| 6.6 | 2.7| 5.9 | 3.0 28.6 | 35.0) 26.2 28.0 | 5.6
48.5 | 15.0 | 13.4 | 10.4| 14.0 |__| 10.4] 6.9| 6.2 | 3.0| 6.5 | 12.0] 4.0] 5.1] 1.8 | 4.7/3.3] 5.5] 3.6] 6.1 | 1.0] 31.0] 35.0} 28.5 | 28.5 | 4.6
18.2 | 14.5 | 12.6 | 10.4 | 13.1| 13.0| 10.3] 7.0| 6.4|2.7|7.2|10.6|3.8| 4.3] 2.5 |4.5/3.5|6.6| 3.3] 5.8 | 3.5] 29.0) 36.4 | 26.3 | 29.0 5.0
90.0 | 15.0 | 13.1 | 11.3 | 14.4 | 18.1) 11.1] 7.4| 6.8 | 3.1 | 7.4| 12.1} 4.1/4.5] 3.0 | 5.4] 3.6| 6.0] 3.4] 6.7 |---| 88.0] 37.5 | 29.5 | 29.5 | 4.6
17.8 | 14.8| 12.5 | 10.6 | 13.1 | 12.3 10.3] 6.6 | 6.1| 3.0) 7.1) 10.8 | 4.1/4.4) 2.0 | 4.7/3.4) 5.7} 8.6) 5.4 | 1.0 | 30.6 | 35.5) 27.3 27.3 | 5.1
15.1 | 12.8 | 10.5 | 14.0 | 15.6 | 10.5| 7.1 6.4] 3.0| 7.4) 10.7] 3.7) 4.0| 1.6 |5.2|3.8| 6.6 | 8.4] 5.7 | 3.5 | 31.0 | 36.6 | 27.6 | 28.7 | 5.2
15.4 | 13.0} 10.8 | 14.2 | 13.0 | 11.0) 8.3 | 7.6 | 3.1 9.0 13.2| 4.3/5.6] 1.3 |4.8|3.7|6.5|3.5| 6.2 | 4.0) 32.0 36.6 | 29.5 | 28.0 5.3
14.4| 12.3 | 10.5) 12.9 | 12.4| 10.0| 7.1 6.5| 3.2 | 6.3 | 11.6 | 3.5/4.9| 1.8 | 42|3.3| 5.5/3.0) 6.3 | 2.0) 28.8] 36.6 | 26.0/ 29.0) 4.4
14.4/12.5/10.3|12.5|12.0| 9.8/6.8) 6.2| 2.7/6.8] 10.6 | 4.0/4.8] 1.8 |4.5 | 3.2| 6.0 3.6 | 5.7 | 3.0 | 29.0 | 35.6 | 27.0 27.8 | 4.8
14.8 | 13.0] 10.7/ 13.8 | 13.0 | 10.3| 6.6| 6.5| 2.7] 7.8| 10.0 | 4.1} 4.4| 2.5 /4.1/ 34 6.2|3.4] 6.3 34.8 |
16.0 | 12.5 | 10.5 | 13.6 | 12.7 | 10.3] 7.0| 6.4| 2.6 | 6.6| 11.1/ 3.7] 4.5] 2.0 | 5.1/3.4] 5.4/3.1] 6.1
15.0 | 12.6 | 10.8 | 13.8 | 13.7 | 11.2 | 6.7 | 6.3 | 2.7/5.7] 11.6 | 4.1 | 4.0} 2.3 |5.2|3.1|6.4|3.8| 6.0 : | 29.6 |
15.1] 12.7 | 11.2|14.0| 12.4] 11.0| 7.2) 6.0| 2.7] 7.3 | 11.7 | 4.2 | 5.0] 2.2 | 5.2/3.8] 6.2) 8.5] 5.0 |__| 32.0] 35.0 | 28.2 | 30.0 | 5.0 |
15.5 | 12.7) 10.7 | 14.4| 14.0| 11.0] 7.7| 7.1/3.2 | 8.1| 18.0/3.8 | 5.1] 2.1 | 5.0) 3.1/5.8] 3.2) 6.5 |__| 31.0 | 36,0| 29.0/ 31.0) 4.8 |
14.7| 12.5 | 10.4 | 18.6 | 12.3 | 11.0| 7.6 | 6.9] 3.0| 6.3 | 12.0 | 4.0 | 5.0) 2.7 | 5.4| 3.8) 5.8/3.4) 6.3 |__| 30.2) 31.8 | 28.2) 26.2) 5.1
14.7 | 12.5 | 10.2| 13.1] 12.8 | 10.0 G8) (8) 6.2| 12.0) 8.5/5.3) 1.4) 5.2/3.7) 6.7) 3.2] 6.4 |__| 31.0} 34.8 | 23.6) 29.6 | 5.6
14.7 | 12.6 | 10.2| 13.4] 12.7 | 10.7] 8.4} 7.2) 8.8] 7.5] 12.3 / 4.2) 5.4/2.4) 5.2/3.7) 6.4/3.4] 6.3 |__| 30.4 | 84.3 | 28.0 / 28.2) 5.3 |
- 15.0 | 13.6 | 10.5 | 13.6| 12.5| 10.0] 7.2| 6.6 3.1/6.8| 11.6 | 4.0} 4.7) 2.5 |5.0|4.0/6.3)3.3) 6.4 |} | eee eas 5.0
if 15.5|12.3| 9.6|13.0|12.4| 10.5| 7.4|6.5| 2.5/5.4) 12.0) 3.8) 5.3] 1.7 |4.7| 3.5] 5.6/3.3) 5.7 |r Se ea |e | 5.7
‘- 14.3| 12.8 | 10.3 12.7|13.0| 10.0] 7.5|6.7|3.0| 7.0] 11.9|3.8|5.1| 2.0 | 4.8|3.6|6.0|3,6| 6.4 |_| ||| 5.2
) ii.4 | 147/126 | 10.4/18.4 42.8110.5|71165| 2.9/6.9) 11.5| 3.9|4.8| 2.05|4.9|3.5|6.1|3.3| 6.09|___-|30.5| 95.4| 27.6 | 28.1] 5.1
l" if
}
BEAN AND PLANTA,
|
|
TabLteE 1V.—Men of Cainta,
=I i= be be Cay Col ee 4 Et ae
be | 82 | 82 | Ba |2.|2,| 28/2 24] BS
ee sl | Sy PE) | 2 | Ses) See a ree EP ee
Species, | 8/52 | £8 | 52 | 25 | 82) fe) eo) e2 | 22) es
a| | ee | s¥)2p|e2|2- | 38/32/88) Es
5 Qa a fa! O74] 9a Gy Qn OS )/oc ! Oa
Z| % 4 re a te fa ie ia ie
{iberian@=s=ees 1 37.7 | 28.7 36.1 | 22.7 | 16.2 | 10.1 | 25.1 | 15.7 | 29.7 | 18.6
Tberian_________- 2) 34.3} 22.7] 32.5} 21.5] 16.2 | 40.7] 21.2] 14.0] 29.8) 198
3] 42.8) 242] 46.2 | 26.2 | 20,0] 11.3] 27.0} 15.3] 36.0] 20.4
4| 35.2] 22.3] 40.6] 25.8] 17.6] 11.1/ 23.6] 15.0] 32.6 | 90.7
5 | 33.2) 22.4) 35.8 | 24.1 | 16.8} 11.3] 19.7 | 13.3] 31.1] 20.9
6| 38.2) 23.7) 38.9} 24.1) 17.3) 10.7] 24.3) 15.0| 33.4! 20.7
7| 38.0) 23.5 | 40.5 | 25.0] 18.5 | 11.4 | 25.0) 15.4] 32.5! 201
8| 40.6] 25.2] 41.0} 25.4} 17.2 | 10.6} 25.0] 15.5 | 33.0! 90.4
Blend ___ 9} 382] 23.8) 39.3} 24.5] 18.0] 11.2} 26.0] 16.2) 31.0! 193
Australoid_______ 10| 39.8] 93.9] 42.4] 25.5] 19.0| 11.4 27.0| 16.2| 31.4| 18.9
41.6] 24.5] 42.1 | 24.8) 19.1 | 11.2} 27.8} 16.4] 331) 19.5
36.2} 23.5] 937.5| 24.3) 18.0] 11.6| 22.0} 14.2} 29.0] 18.8
35.9] 21,8] 41.7 | 25.4] 16.5] 10.0] 23.5] 14.3) 36.0) 921.9
40.7| 24.0} 43.5 | 25.7} 19.0] 11.5} 28.0) 16.5 | 32.9) 19.4
37.2| 22.7] 46.7 | 28.5} 20.0] 12.2} 24.0] 14.6 | 32.2| 19.6
36.8| 22.1] 48.3] 26.0] 16.5 | 9.9) 25.7| 15.4] 35.6) 214
37.5 | 22.4] 48.0} 28.7] 18.5 | 11.0] 26.5} 15.8] 33.4! 20.0
39.6 | 24.5] 40.8| 25.3] 17.4 | 10.7 | 24.2] 15.0| 33.6! 20.8
pense 19 37.1 23.6 40.0 | 25.4 | 17.0] 10.8 | 22.6} 14.3 | 32.4 20.6
Iberian___------- 20] 38.7) 24.4) 938.6] 24.3] 17.7] 11.1] 22.5) 14.1 | 36.3) 220
Blend ___.-------| 21] 36.3] 23,8) 389.5] 25.8| 19.0} 12.4] 93.5) 15.4| 32.5/| 213
Australoid | 35.8| 22.6] 41.0] 25.9] 18.0] 11.3] 23.0| 14.5] 33.5! 21.2
Elend eee 37.0 | 23.7] 37.5 | 24.1) 16.5] 10.6 | 24.0] 15.4] 32.0} 20.5
Australoid 39.2} 24.9] 38.0} 24.2 | 20.0] 12.7] 23.0] 14.6] 32.8] 20.8
Blend =e 39.2 | 245] 41.0| 25.6 | 17.0} 10.6 | 23.0] 14.3] 28.0) 17.5
Blends BELO) |e 40.5 )------ 18.0 |___-_- 93.0 |------ 3210) eee
Blend __- 37.0| 22.9] 43.5] 27.0] 17.8] 11.0] 241] 14.9] 31.7] 19.6
Australoid 38.2 | 24.6) 38.0] 24.5] 18.0] 11.6 | 22.0] 141] 288] 18.5
Blend ___ 38.2 | 24.0] 36.2 | 22.7] 17.0] 10.6 | 24.0] 15.0] 30.5] 19.1
Australoid_------| 30} 39.7] 23.8 | 43.5 | 26.1] 18.0] 10.8 | 27.5 | 16.5] 34.74 20.8
Blend ___ 33.3 | 21.9| 40.0] 26.3] 17.7] 11.6] 22.3) 14.6] 29.5| 19.4
Iberian _--------- 37.4| 23.0] 42.4 | 26.1 |-17.5 | 10.8} 24.0] 14.8] 32.0| 19.7
Iberian _--------- 39.8| 24.3 40.6 | 24.8] 19.2] 11.7] 25.0] 15.2] 33.5] 20.5
Tberian ---------- 39.9 | 24.2 | 42.0] 25.4] 18.0] 10.9] 25.0] 15.1] 34.0] 20.6
Tberian ---------- 40.2| 23.7| 45.5 | 26.9} 19.5] 11.5) 25.5 | 15.0] 33.5] 19.8
Australoid 35.9 | 22.2| 42.6} 26.3] 18.6 | 11.5] 23.4 | 14.4] 312] 19.3
Aipine eee 41.7| 26.2 | 38.5 | 24.2] 18.6) 11.7] 26.3] 16.5] 30.7] 19.3
Tberian_____---_- 40.7| 24.0| 45.0 | 26.6} 19.1] 11.3] 26.9] 15.9] 35.6] 21.0
General average--| 37.9 | 23.6 | 40.78 | 25.2 | 18.0] 11.1} 24.3] 15.1) 32.4] 20.0+
Pubis to umbi-
licus.
a
Sale
N
THE
indices and relative factors.
i
|
|
Seemroute atl
leflo.jadi"3| 2 | 8
\se(ae|_2/.2| 2 | 2
BS |a>i(ssl|aa| 2 | ¢
He lg ilo |e S Z
lp |6 Je |S 3 | z
| 38.8! 283] 212| 9.7] 738] 76.6
31.8 | 32.0 23.8] 123] 84.6] 72.6
34.5 | 39.4| 26.6 | 14.4] 79.9]. 84.0
32.2 | 37.2] 24.3 | 13.6] 814] 77.1
92.7 | 37.6] 246 | 12.9/ 82,9] 90.0
| 34.0 | 40,3] 22.3 10.5| 78.9 | 85.4
| 32.5] 45.8] 24.5) 12.5] 84.6] 66.0
28.0 | 62.5 | 23.0| 11.8] 844] 96.9
38.3 | 48.4 | 25.5 | 13.5| 83.7| 81.9
32.7 | 42.5 | 24.0| 12.8) 77.7} 102.1
35.0 | 37.1 | 23.9| 12.1) 77.9] 81.6
33.0 |------ 23,0 | 12.5} 80.6] 90.4
36.4 | 35.9] 23.0| 11.7/ 80.2] 80.8
36.0 | 41.6} 21.0] 10.0] 87.5] 84.0
35.8 | 35.9 | 22.0] 10.5] 75.9] 77.7
37.0} 40.5} 21.5] 102! 75.4] 863
34.5 | 42.0| 23.7| 12.7] 80.3] 88.8
30.8 | 47.0 | 222] 10.6] 73.8| 93.6
35,7 | 32.7| 22.7| 106) 77.0! 74.6
35.3 | 41.9] 22.8] 10.8] 81.0] 78.4
30.4| 381] 24.0] 13.4] 79.7| 88.4
35.0 | 40.0 26.0] 13.9) 75.0) 911
32.5 | 32.3| 21.5] 10.7| si4} 93.2
31.0| 41.9| 22.0] 11.3] 80.7] 95.2
32.0 | 40.6 | 27.0| 13.8| 81.1) 76.7
Blau spas feee ee 80.0} 714
37.0 | 32.4 | 24.0] 13.4] 79.1) 983.3
33.5 | 38.8} 23.0] 13.0] 80.9| 93.2
31.7 | 45.1 | 22.3] 11.2] 87.4| 82.2
31.6| 47.4 | 13.9] (2) | 80.2! 102.5
35.0 | 28.5 | 23.6] 11.9] 81.6] 84.0
36.0| 34.7| 21.0] 8.0] 81.2) 74.5
33,5 | 38.5 | 23.0| 11.5] 82.6] 80.0
35.0 | 40.0| 22.8] 10.8! 75.0| 66.0
38.5 | 25.9) 25.0| 12.7] 79.0] 77.7
341 | 43.4] 24.7] 181) 75.0] 85.1
38.6 | 29.1| 23.5} 115] 90.1 | 71.7
34.0] 42.6| 23.5] 11.6] 78.6] 74.5
33.8 | 39.5| 23.4| 11.8] 80.4| 828
MEN OF CAINTA.
13
Ear type.
| Morphologie
berian) Cand) Dasa psaea eee -—
B. B. B. Iberian C
Iberian A and D
Iberian A __-
Mixed Primitive
Iberian B Primitive
PIUMitl vies 2s ee eee
Iberian D, Mixed Alpine Primitive_____
Iberian A Primitive___________ Gee ee
Terrien 6 hess: See oo ees
Mberian iy Mixed sene eee
Mixed Iberian D subnorthern -_________
Tiberian’ D Bs bs ieee ee
Mixed Primitive, Iberian ___-----_-_----
Mixed Primitive subnorthern___________
Mixed Alpine Primitive --__---_-___-____
Odd type, Alpine, Primitive -______-____
Mixed subnorthern_
Mixed B. B. B., Primitive Iberian _____.
beniansD Sm ix ed aeeee e
Mberian’D ian Ci Cea ee ee eee
TherianyAy and i) Sse sae ees
MixediBiB 9s) sPrimitives =a
Iberian, mixed
Iberian A, B, D
Wirb-qotal as} 15} 1}, Leta OR |
IVGIX COR ee Ban Sees ook aa
face index,
Physiognomic
face index.
14 BEAN AND PLANTA.
side bust views of these men have been published already with the men
of Taytay* to illustrate the Iberian type.
Absence of the Primitive is noteworthy at Cainta, and there is no
modified Primitive or any form resembling them except the Blend. A
few Australoid and Alpine types are seen and these with the Blends
indicate to some extent the Filipino mixture.
Enough has been given to demonstrate the similarity of the Cainta
men to the European, and to the Hast Indian. Their presence proves
that such people came to the Philippines, and the presence of similar
types throughout the Islands indicates an Indian influence. This has
been no inconsiderable factor in the peopling of the Philippines and
explains the great prevalence of the Iberian throughout the archipelago.
In support of this view, the recent work of Saleeby* concerning the
Hindu influence previous to the more recent Spanish occupation and
before the Moro or Mohammedan invasion of the Islands, is worth noting.
*This Journal, Sec. A. (1909), 4, 359. ;
* Studies in Moro History, Law and Religion. Ethnolog. Surv. Pub. Manila
(1905), 4, Part I.
BEAN AND PLANTA: THE MEN OF CAINTA,.] [Patn. Journ. Sct, Vou. VI, No. 1.
iG. 3 (No. 18),
Fic. 1 'No. 38). Fic. 2 (No. 19). Fi
PLATE 1.
THE PHILIPPINE JOURNAL OF SCIENCE,
D. General Biology, Ethnology and Anthropology.
Vol. VI, No. 1, February, 1911.
BORKENKAFER DER PHILIPPINEN.
Von H. STROHMEYER.
(Minster Ober-E lsass, Germany.)
ERSTE SERIE.
Uber die Borkenkifer-Fauna der Philippinen ist bisher sehr wenig
bekannt geworden. WHichhoff beschreibt in seiner Monographie zwei
dortige Arten respective eine davon Varietat: Xyleborus kraatzti var.
philippinensis,+ und Coccotrypes pygmaeus? Wichh. Hine weitere yon
den Philippinen bekannte Art ist: Xyleborus capito Schauf.2 Hagedorn
erwihnt das Vorkommen yon Hurydactylus sexspinosus Motsch. auf
Iuzon.* Fast ebenso unbedeutend wie die Zahl der von den Philippinen
bekannten Ipiden (Scolytiden) ist diejenige der Platypodiden. Chapuis
nennt nur vier Arten:’ Crossotarsus lecontei Chap., Platypus setaceus
Chap., Pl. turbatus Chap. und Pl. lepidus Chap. Hine fiinfte Art: Pl.
philippinensis © fiigte spiter Blandford hinzu.
Auf Grund des Studiums der Borkenkéfer aus der staatlichen
Sammlung in Manila bin ich in der Lage weitere Beitrage zur Kenntnis
dieser forst- und landwirtschaftlich schidlichen Insekten zu liefern und
zwar nicht nur auf rei systematischem, sondern auch auf biologischem
Gebiete.
Unter den nachfolgend aufgeftihrten zwolf Borkenkiferarten sind
zehn neu fiir diese Inselgruppe, fiinf hiervon waren bisher tberhaupt
noch nicht beschrieben.
1 Hichhoff, Ratio, descriptio, emendatio Tomicinorum (1878), 374.
2 Loe. cit. (1879), 310.
® Schaufuss, Tijdschr. voor Ent. (1897), 40, 215.
“Deutsche Ent. Ztschr. (1908), 377.
* Chapuis, Monographie des Platypides (1868).
°‘Trans. Hnt. Soc. London (1896), 193.
101096——2 17
18 STROHMEYER.
IPID (Scolytidee).
I. Prnipentat Zz.’
PHL@OTRUPIN A.
DACTYLIPALPUS Chapuis.
Dactylipalpus transversus Chapuis.
Dactylipalpus quadratocollis Chapuis, Synops. des Scolyt., Mem. Soc. Roy.
Sci. Liége (1869), 12; Strohmeyer, Entomol. Blatter (1909), Heft. 12.
Minporo, Rio Baco, P. I. (3388, 8. C. McGregor).
Diese Art war bisher nur bekannt yon Malacca, Ternate, Celebes und
Sumatra. D. quadratocollis Chap. ziehe ich als Synonym zu D. trans-
versus nachdem ich durch Untersuchung der Geschlechtsorgane auch
bei afrikanischen Dactylipalpus-Arten festgestellt habe, das der Querein-
druck auf dem Halsschilde ein s. g. sekundirer Geschlechtscharakter des
Weibchens und kein Artkennzeichen ist. Die weiteren yon Chapuis bei
quadratocollis genannten Unterscheidungsmerkmale; geringere Grdsse
und mehr quadratisches Halsschild sind nur Higentiimlichkeiten der
schmileren und meist kleineren Mannchen.*®
Il. SprintpentTat az.’
HYLESINID.
SPHAZROTRYPES Blandford.
Sphzerotrypes philippinensis sp. nov.
Brevissime ovatus, piceus vel nigropiceus, antennis tarsisque dilu-
tioribus rufescentibus; capite nigropiceo, vertice in fundo subtilissime
reticulato haud dense sed fortiter punctato ; fronte plana rugose punctata,
squamulis flavis ac pilis parvis sat dense adspersa, supra cs plerunque
carinula longitudinali brevi laevi; prothorace sat nitido valde transverso,
anterius fortiter angustato, basi postice acutius producta, ad latera
eyidenter marginato, post apicem constricto, in fundo subtilissime
reticulato haud dense punctato punctis magnis squamiferis irregulariter
dispositis, praesertim antice brevissime tomentoso et pilis singulis flavis
adsperso, linea mediana plus minusve obsoleta; elytris prothorace latio-
*Haged., Ent. Blitter (1909), 5, 163.
*Zu vergl. meine Arbeit in den Entomologischen Blaittern, Jahrg. 1909, Heft
12: “Beschreibung zweier neuer Phlcwoborus-Arten und Erginzung der Diagnosen
einiger bekannter Phleotrupiden) unter Beriicksichtigung der sekundiiren Ge-
schlechtscharaktere.”
BORKENKAFER DER PHILIPPINEN. 19
tibus, striato-punctatis, punctis rotundis distantibus, striis basin versus
angustatis et ante marginem anteriorem abbreviatis, interstitiis striis
multo latioribus elevatis, ante marginem basalem valde dilatatis, et
transverse rugosis, fortiter et irregulariter punctatis punctis squamiferis,
praesertim in disco tuberculis majoribus uniseriatim dispositis et antice
in carinulam plus minusye confluentibus; abdomine subtus fortiter ac
dense punctato.
Longitudo 3.2-3.5 mm.; latitudo prothoracis 1.9-2.1 mm.; latitudo
elytrorum 2.1—2.3 mm.
Mrnpanao, Zamboanga, P. I. (W. I. Hutchinson legit).
Futterpflanze: Yacal (Hopea).
1 Type No. 8849 in der Entomologischen Sammlung des Bureau of
Science, Manila, P. I.
1 Paratype in meiner Sammlung.
Kurz eiformig, heller oder dunkler pechbraun mit etwas helleren mehr
rotlich-braunen Antennen und Tarsen; Kopf dunkel pechfarben, Scheitel
auf chagriniertem Grunde kraftig aber nicht sehr dicht punktiert; Stirn
flach, grob punktiert, ziemlich dicht mit gelblichen Schuppen und kleinen
Haaren besetzt, tiber den Mundteilen mit einem zuweilen fehlenden
kurzen und glattem Lingskiele; Prothorax missig glinzend, breiter als
lang, nach vorn stark verschmilert und vor der Spitze eingeschniirt, an
der Basis hinten in der Mitte mit vorgezogener Spitze, an den Seiten deut-
lich gerandet auf fein chagriniertem Grunde ungleich und missig dicht
_punktiert, die schuppentragenden Punkte gross und nur flach einge-
driickt, besonders der vordere Teil des Halsschildes oben kurz und dicht
behaart mit einzelnen zwischenstehenden lingeren Borsten, die Mittelli-
nie ziemlich undeutlich und bei den einzelnen Hxemplaren ungleich
ausgebildet; Fliigeldecken etwas breiter als das Halsschild, in deutlich
ausgeprigten Streifen punktiert, die Punktstreifen vor der etwas wul-
stigen Basis sehr verschmilert und abgekiirzt, die Zwischenraume zwischen
den Streifen breiter als die Punktstreifen, vor der Basis mehr oder weni-
ger miteinander verschmelzend, gewolbt und unregelmassig punktiert
mit schuppentragenden Punkten, hauptsiichlich auf der Scheibe mit je
einer Reihe weitliufig gestellter Tuberkeln welche nach der Basis hin
mehr oder weniger zu einer Leiste zusammenfliessen, die verbreiterten
Teile der Zwischenriume an der Basis quer gerunzelt; Abdomen auf der
Unterseite stark und dicht punktiert.
In Fig. 1 und 2 sind Mentum und Maxillen abgebildet.
Von Spherotrypes siwalikensis Stebbing unterscheidet sich diesse Art
unter Anderem durch das Fehlen des hinteren Quereindruckes auf dem
Halsschilde, von Sph. coimbatorensis Stebbing durch die Sculptur des
Prothorax und yon Sph. pila und globulus Blandford durch die Beschaf-
fenheit der Fliigeldecken. Das glattere und nur massig dicht punktierte
20 : STROHMEYER.
Halsschild schliesst auch eine Verwechslung dieser Art mit Spherotrypes
tanganus Schautfuss, blandfordi Schaufuss und barbatus Hagedorn aus.
Fig. 1. é Fig. 2.
Fies. 1 und 2.—Spherotrypes philippinensis Strohmeyer.
Mentum, palpi labiales et maxilla. 80 X* vergrossert.
Gefangen wurden die mir vorliegenden Hxemplare von Sphwrotrypes
philippinensis m. an Yakal, emem Hartholze der Gattung Hopea.
Die Frassfigur (Tafel 1) besteht aus einem einarmigen Lotgange ohne
~Rammelkammer (nuptial chamber) und zahlreichen sich nicht kreuzen-
den Larvengingen. Der Muttergang, welcher meist oben an der Spitze
mehr oder weniger nach einer Seite gekriimmt ist, hat eime Linge yon
3.5 bis 4.5 em. Die Higruben, in welche die Hier einzeln abgeleg werden,
sind ausserst dicht aneinander gereiht. Die verhaltnismassig kurzen und
breiten Larvenginge fallen dadurch auf, dass sie sehr frth an Breite
zunehmen, eine T'atsache, die auf ein sehr rasches Wachstum deutet. Die
Puppenwiegen liegen am Hnde der Larvenginge, welche in Splint und
Rinde ungefahr gleich tief emschneiden.
Nach Stebbings Abbildung zu urteilen sind die Mutterginge von Sphe-
rotrypes suwalikensis Stebbing *° kirzer und die Higruben weniger dicht
aneinander gedraingt. Letztgenannter Kifer lebt an Shorea robusta.
CRYPHALIN 2.
CRYPHALUS Erichson.
Cryphalus squamulosus sp. nov.
Blongatus, fere cylindricus, pallide flavescens, prothorace anteriori
et capite rufescentibus; oculis reniformibus antice emarginatis; vertice
subtilissime rugoso fere laevi; fronte subplana dense rugoso-punctata ;
prothorace semi-elliptico latitudine vix breviore, lateribus a basi’ ad me-
diam partem rectis parallelis, dein ad apicem fortiter rotundatis, angulis
posticis subrotundatis, supra medio subgibbo, margine anteriori unise-
® Nach den mir vorliegenden 4 Frassfiguren.
1 Departamental Notes on Insects that affect Forestry, EH. P. Stebbing, Calcutta
(1902), pl. XXIII.
BORKENKAFER DER PHILIPPINEN. 21
riatim tuberculato, disco antice tuberculis transversis compressis valde
infuscatis subconcentrice ordinatis, ad basim et latera subgranulate punc-
tato, antice pilis, postice squamulis albidis adsperso ; elytris subeylindricis,
latitudine multo longioribus, striato-punctatis, punctis magnis, striis
haud impressis, interstitiis planis, vix perspicue uniseriatim punctatis,
punctis minimis, multo magis distantibus quam in striis, squamulis ac
pilis albidis uniseriatim dispositis.
Long. 1.36 mm., lat. 0.53 mm.; prothoracis longitudo: 0.50 mim. ;
prothoracis latitudo: 0.53 mm.; elytrorum longitudo: 0.86 mm.; elytro-
rum latitudo: 0.53 mm.
Minvoro, Calapan, P. I. (J. L. Webb legit).
Type No. 1420 in der Entomologischen Sammlung des Bureau of
Science, Manila, P. I.
1 Cotype in meiner Sammlung.
Lang gestreckt, fast cylinderformig, blass gelb, Kopf und yorderer
Teil des Prothorax rothchgelb; Augen vorn ausgerandet; Scheitel dus-
serst fein gerunzelt, fast glatt; Stirn wenig gewolbt, fast flach, dicht und
erob punktiert; Halsschild etwas kiirzer als breit, die Seiten von der
Basis bis tiber die Mitte hinaus gerade und parallel, hierauf bis zur Spitze
stark gerundet, die Hinterecken nur wenig abgerun-
det, oben in der Mitte stark erhoéht, am Vorderrande
mit einer Reihe von Tuberkeln, vorn auf der Scheibe
mit zahlreichen quergestellten schmalen Hoéckerchen,
welche fast in concentrischen Kreisen angeordnet
sind, nach der Basis hin und auf den Seiten kornig
punktiert, yorne mit Haaren, nach hinten mit ein-
zelnen bless-gelben Schuppen bedeckt. Die Fliigel-
decken fast cylinderformig, viel langer als breit, in
Reihen gross punktiert, die Zwischenriume flach und
jiusserst fein einreihig punktiert, die Punkte viel Sate een
weiter auseinanderstehend als in den Punktstreifen, strohmeyer. An-
zwischen den Streifen abwechselnd Reihen yon enna. 12 x ver-
Schuppen und Haaren. oon
-Auffallend gross ist bei diesem Cryphalus das erste Glied der Fihler-
geisel, (funiculus) (Fig. 3). Wegen der ausgerandeten Augen gehort
der Kifer in die erste der von Hichhoff gebildeten Cryphalus-Gruppen.
IPIN 4.
COCCOTRYPES Hichhoff.
Coccotrypes graniceps Hichhoff. 5
Coccotrypes graniceps Hichhoff, Ratio, descriptio, emendatio Tomicinorum
(1878), 314.
Necros, Maao, P. I. (1400, Charles S. Banks).
Futterpflanze: Cacao (Theobroma cacao Linn.)
Hin Exemplar in meiner Sammlung.
DO - STROHMEYER.
Hichhoff’s Beschreibung passt sehr gut auf beide Exemplare nur fehlt
den mir vorliegenden die kleine Stirnleiste. Dieses Merkmal ist aber bei
vielen Borkenkaferarten sehr wenig constant, manchmal auch nur Ge-
schlechtskennzeichen, jedenfalls gentigt es nicht um diese Exemplare als
eime andere Art anzusehen.
Bisher war dieser Kafer nur in Japan gefunden worden.
OZOPEMON Hagedorn.
Ozopemon laevis sp. nov. ,
Femina: oblonga, cylindrica, nitida, parce pilosa, flava, prothorace
anteriore et capite flavo-ferruginea, elytris antice flavis, postice flavo-
ferrugineis, irregulariter infuscatis; yertice tenuissime strigoso-punctato,
linea mediana, valde infuscata; fronte antice leviter impressa, fortiter
punctata, punctis magnis, linea mediana elevata, angusta non infuscata,
prothorace fere globoso, latitudine yix breviore, lateribus leviter apice
fortiter rotundato, angulis porticis rotundatis, dorso convexo subgibbo,
anterius et in lateribus tuberculis vel rugis transversis infuscatis, subcon-
centrice ordinatis scabrato, postice in disco evidenter sat dense punctato ;
elytris cylindricis, prothorace vix latioribus et illo prope duplo longiori-
bus, humeris rotundatis, lateribus longe ultra medium parallelis, dein
fortiter conjunctim rotundatis, striato-punctatis, punctis sat magnis et
confertis, striis antice haud postice obsolete impressis, interstitiis fere
planis, laevibus, uniseriatim punctatis punctis minoribus quam in striis et
magnis distantibus, apice retuso plano, interstitiis uniseriatim tubercu-
latis, tuberculis piliferis; abdomine subtus punctato et sparsim aequaliter
pilosa.
Long. 4.1 mm., latitudo maxima 1.7 mm.; prothoracis longitudo 1.4
mm., latitudo 1.6 mm.; elytrorum longitudo 2.7 mm., latitudo 1.7 mm.
Minporo, Calapan, P. I. (J. L. Webb legit).
Type 2 No. 1421 in der Entomologischen Sammlung des Bureau of
Science, Manila, P. I.
_ Paratype, 2, im meiner Sammlung.
Weibchen. lLanglich, cylindrisch, glanzend, diinn behaart, gelb, vor-
derer Teil des Halsschildes und Kopf rotlichgelb, Fliigeldecken an der
Basis gelb, nach hinten rotlichgelb mit unregelmassig verteilten dunkleren
Triibungen, Scheitel sehr fein gestichelt punktiert, mit brauner Mittel-
linie; Stirn vorn leicht eingedriickt, stark punktiert, mit sehr schmaler
etwas erhohter Mittellinie; Halsschild fast kugelig, etwas breiter als lang,
an den Seiten leicht, an der Spitze stark gerundet, nach vorn etwas ver-
schmalert, Hinterecken stark gerundet, oben stark convex, vorn und auf
den Seiten mit dunkleren quergestellten schmalen Kornchen, die fast in
concentrischen Kreisen angeordnet sind, hinten auf der Scheibe deutlich
und ziemlich dicht punktiert; Fliigeldecken cylindrisch, wenig breiter
“ Deutsche Ent. Ztschr. (1908), 382, und dieselbe Ztschr. (1910), 1, 2 und 3;
Fig. 43a, 1. m.
BORKENKAFER DER PHILIPPINEN. 23
als das Halsschild und fast doppelt so lang als dieses, Schultern gerundet,
Seiten weit tiber die Mitte parallel, dann
nach hinten stark gerundet, in Streifen
punktiert, die Punkte ziemlich gross und
dicht aneinandergereiht, die Streifen nur
nach hinten leicht vertieft, die Zwischen- ic. 4—ozopemon laevis Stroh-
riume fast eben und je mit einer Punktreihe Pek ee (scapus et
versehen, die Punkte kleiner und weitliu- ,
figer als in den Streifen. Absturz abgeflacht, die Zwischenriiume hier
je mit einer haartragenden Kérnchenreihe ; Abdomen unterseits punktiert
und diinn gleichmissig behaart.
Dieser Kafer gehort einer fiusserst interessanten Gattung
an, tiber deren Lebenweise noch gar nichts bekannt ist.
Die Maxillarbewaffung (s. Abb.) welche aus breiten siche!-
formigen Dornen besteht, deutet jedoch darauf hin, dass
wit es mit einem Basthbewohner und keinem technisch
schiidlichen Holz-Insekte zu tun haben, trotzdem die iius-
sere Form sehr an Xyleborus-Arten erinnert, zumal das
Halsschild ziemlich deutlich gebucicelt ist.
Fie. 5.—Ozope-
mon laevis
Strohmeyer.
Oblongus, cylindricus, nitidus, parce pilosus, nigropi- Mentum
ceus, prothorace, capite, antennis pedibusque rufescentibus ; ees.
fronte nitida, obsolete punctata, antice leviter impressa;
prothorace latitudine vix breviore, lateribus, fere rectis, apice fortiter,
rotundato, angulis posticis subrectis vix rotundatis, dorso convexo sub-
gibbo, anterius et in lateribus tuberculis vel rugis
transyersis subconcentrice ordinatis scabrato,
postice subtilissime parce punctato, nitido; elytris
eylindricis, prothorace vix latrioribus et illo prope
duplo longioribus, humeris rotundatis, lateribus
fere usque ad apicem parallelis, dein fortiter con-
junctim rotundatis, striato-punctatis, punctis
parvis non confertis, striis haud impressis, inter- HS recone eae
stitiis latis planis laevibus alternatim irregulariter
uni- vel biseriatim parcius punctatis, punctis minoribus et multo magis
quam in striis distantibus; declivitate postica subtruncatoretusa, con-
vexiuscula, ambitu postice acutius marginato, interstitiis uniseriatim
tuberculatis, tuberculis aureo setosis.
Longitudo 6.0 mm. ; longitudo thoracis 2.1 mm.
Luzon, Bataan, Limay, P. I. (R. J. Alvarez legit).
Type No. 12007 in der Entomologischen Sammlung des Bureau of
Science, Manila, P. I.
Paratype in meiner Sammlung.
Langgestreckt, cylinderformig, glinzend, wenig behaart, dunkel pech-
farben; Halsschild, Kopf, Antennen und Beine rotlich-braun. Stirn
Ozopemon major sp. nov.
24 STROHMEYER.
glinzend undeutlich punktiert mit emmem wenig vertieften Liangsein-
drucke in der Mitte; Halsschild kaum kiivzer als lang, Seiten fast gerade,
vorn stark gerundet, Hinterecken fast rechtwinkelig, wenig abgerundet,
oben stark conyex, in der Mitte etwas gebukelt, auf der vorderen Hilfte
und auf den Seiten quergerunzelt, die Erhéhungen beinahe in concentri-
schen Kreisen angeordnet, hinten glatt sehr sparsam und fein punktiert,
glinzend ; Fliigeldecken cylinderformig, kaum breiter als das Halsschild
aber fast doppelt so lang, die Schultern gerundet, die Seiten weit iiber
die Mitte parallel, alsdann gemeinsam gerundet, in Streifen punktiert, die
Punkte klein und nicht sehr dicht gestellt die Streifen nicht vertieft, die
Zwischenriume breit, eben, glatt, abwechselnd unregelmissig ein- und
- gweireihig punktiert mit dusserst feinen weit getrennt stehenden Punk-
ten; Fliigeldecken-Absturz ziemlich abschtissig, wenig gewolbt, nach
hinten ziemlich scharf gerandet, die Zwischenraéume hier mit je einer
Reihe goldgelbe Haare tragenden K6rnchen.
Diese Ozopemon-Art ist die grosste under allen bisher beschriebenen
und ahnelt bei oberflichlicher Betrachtung in der Form sehr einem Bos-
trychiden aus der Gattung Sinoxylon.
Bisher sind nur die folgenden Arten dieser Gattung bekannt geworden:
Ozopemon rugatus Blandford (Sarawak, Borneo).
Ozopemon sumatranus Blandford (Sumatra, Mt. Singalang).
Ozopemon gravidus Blandford (Sarawak, Borneo).
Ozopemon regius Hagedorn (Sumatra).
Ozopemon theklae Hagedorn (Sumatra).
yar. sirambeanus Hagedorn (Si-Rambé, Sumatra).
var. singalangicus Hagedorn (Mt. Singalang, Sumatra).
Ozopemon. obanus Hagedorn (Mentawei Inseln).
Ozopemon fuscicolus Hagedorn (Jaya u. Sumatra).
Ozopemon laevis Strohmeyer (Mindoro, Philippines).
Ozopemon major Strohmeyer (Luzon, Philippines).
Ot He Oo Ww t+
OW AH
Ill. Smrrpentata.”
XYLEBORIN~.
XYLEBORUS Bichhoff.
Xyleborus perforans Wollaston.
Tomicus perforans Woll., Cat. Col. Mad. (1854), 96; Col. Hesperid. (1867),
113.
Xyleborus kraatzii Hichh., Berl. Ent. Ztschr. (1868), 152; Ratio Tomici-
norum (1878), 374; Blandford, W. F. H., Report on the destruction of
bear casks in India, London, 1893.
Nzcros, Maao, P. I. (416 Charles S. Banks).
Ein @ in meiner Sammlung.
Beide Exemplare gohéren der kleinen Horm des X. perforans an,
2 Haged. Ent. Blatter (1909), 5, 163.
BORKENKAFER DER PHILIPPINEN. 25
t
welche Hichhoff noch von der grésseren Form affinis trennte. Als
Fundorte dieser Varietiit waren bicher bekannt: Madeira, Indien, Ceylon,
Andamanen, Tonkin, Siam, Malayische Region, Jamaika, Amazonas,
Sechellen, Madagaskar, Ost-Africa und die Insel Principe. In meiner
Sammlung befinden sich ausserdem Exemplare yon den Cap Verde
Inseln, Upolu (Samoa Ins.) sowie den Aroe- und Key-Inseln.
Xyleborus perforans var. philippinensis Hichh.
Ayleborus kraatzti var. philippinensis Hichhoff, Ratio Tomicinorum (1879),
343.
Xyleborus perforans var. philippinensis Hichhoff; Blandford, Report on the
destruction of beer casks in India by the attacks of a boring beetle
(Xyleborus perforans Woll.) London (1893), 12 u. 46 (Appendix).
Luzon, Laguna, Magdalena, P. I. (No. 410 W. Schultze) 1 2 in
meiner Sammlung.
Futterpflanze: Cocosnuss (Cocos nucifera Linn.)
Diese Kafer unterscheiden sich von den typischen XY. perforans Woll.
(X. kraatzvi Bichh.) durch ihre bedeutendere Grosse, dunklere, briiunliche,
Farbung und die aufallend groben Punktstreifen auf den Fliigeldecken.
Auch sind die Streifen neben der Naht sehr deutlich vertieft. Ich halte
es noch fiir sehr zweifelhaft ob dieser Kifer nur eine Varietat des
perforans ist, die Entscheidung dieser Frage bei eimem Vertreter dieser
fusserst schwer zu bestimmenden Xyleborus-Gruppe muss verschoben
werden his mehr Material vorliegt.
Sobald mehr Exemplare dieser Art besonders auch Miannchen, vorliegen,
wird sich feststellen lassen, ob wir nur eine Varietiit des perforans oder
eine gute Art vor uns haben.
Subgenus Eurydactylus Hagedorn.
Eurydactylus sexspinosus Motschulsky.
Becoptopterus sexspinosus Motsch., Bull. Mosecou (1863), 36, 515.
Xyleborus abnormis Hichhoff, Berl. Ent. Ztschr. (1868), 282.
Ayleborus abnormis Hichhoff, Ratio Tomicinorum (1879), 343.
Piatydactylus abnormis Hichhoff, Notes Leyd. Mus. (1898), 8, p. 25.
Platydactylus sexspinosus Motsch., Blandford Indian Mus. Notes (1893), 3,
§5.
Burydactylus sexspinosus Motsch., Hagedorn, Deutsche Ent. Ztschr. (1909),
733.
Neeros, Mailum, P. I. (6498, Charles S. Banks).
Ein Exemplar in meimer Sammlung.
Als Fundorte waren bisher bekannt: Ceylon, Indien, Jaya, Sumatra,
Philippinen (Luzon), fiir die Varietét H. multispinosus Hagedorn:
Kamerun.*® In meiner Sammlung habe ich ein Exemplar von sez-
spinosus aus Deutsch-Ost-Afrika; Hagedorn sah diesen Kifer auch in
Zanzibar-Kopal. Als Nihrpflanzen sind bis jetzt bekannt: Reis, Kakao
und Kaffeebaum.
8 Deutsche Ent. Ztschr. (1908), 377.
26 STROHMEYER.
PLATYPODID.
CROSSOTARSUS Chapuis.
Gruppe: CROSSOTARSI GENUINI Chapuis.
Crossotarsus comatus Chapuis.
Crossotarsus comatus Chapuis, Monographie des Platypides (1865), 59, fig. 5.
Nueros, Maao, P. I. (417 Charles 8. Banks).
Ein @ in meimer Sammlung.
Diese Art war bisher nur aus Celebes bekannt (Chapuis).
PLATYPUS Herbst.
Gruppe: PLATYPI suLcATI Chapuis.
Platypus jansoni Chapuis.
Platypus jansoni Chapuis, Monographie des Platypides (1865), 244, fig. 146.
Nezeros, Maao, P. I. (413 Charles S. Banks).
Kin ¢ in meiner Sammlung.
Hichhoff kannte diese Art von Neu-Guinea, den Molukken und von
Celebes.
Gruppe: PLATYPI CUPULATI Chapuis.
‘Phatypus schultzei sp. nov.
Mas: elongatus angustus, ferrugineo testaceus elytris apice infuscatis ;
vertice fortiter punctato punctis majoribus, linea mediana levi infuscata ;
fronte rugose punctata, stria mediana parva impressa; prothorace nitido
sparsim irregulariter punctato, lea mediana in postica parte, congeriebus
punctorum duabus minimis ad latera lineae medianae; elytris evidenter
striato-punctatis, stria suturali sulcata, interstitiis laevibus uniseriatim
irregulariter punctatis punctis multo minoribus quam in striis, depres-
sione postica circulari, inferne emarginata, emarginationis margine dente
obtuso armato, angulo suturali obtuso.
Longitudo: 4.0 mm.
Fem: flavescens, fronte rugose punctata, linea mediana parva; pro-
thorace sat dense punctulata, in postica parte congeriebus punctorum
duabus magnis semi-ovalibus ad latera lineae medianae; elytris striato-
punctatis, punctis parvis obsolete impressis, stria suturae proxima im-
pressa, interstitiis sparsim uniseriatim punctulatis punctis minimis.
Longitudo: 4.4 mm.
Neeros, Maao, P. I. (Charles S. Banks legit).
Typen 1 ¢ u.1 2 No. 1594 in der Hntomologischen Sammlung des
Bureau of Science, Manila, P. I.
-“Bekanntlich hat Chapuis die g g u. 9 9 der Platypodiden durchgingig
verwechselt; fig. 5 stellt deshalb nicht wie angegeben das 9 sondern das ¢ dar.
BORKENKAFER DER PHILIPPINEN. iil
Paratypen 1 6 u.1 2 in meiner Sammlung.
Minnchen. Langgestreckt, schmal, rétlichgelb, die Fliigeldecken nach
hinten dunkler; Scheitel stark und grob punktiert
mit glatter dunkler Mittellinie; Stim grob punk-
tiert, mit kurzem strichformigem Hindruck in der
Mitte; Halsschild glinzend unregelmiissig sparsam
punktiert, hinten mit glatter Mittellinie, an den
Seiten dieser Linie je ein kleiner aus wenigen (circa Fic. 7.—Platypus
3 : : Z Cass oo schultzet Stroh-
8-10) deutlichen Punkten gebildeter Flecken ; Flii- Oren, ene
geldecken mit deutlichen Punkstreifen, die beiden et marginatio pos-
tica, 15 X ver-
neben der Naht liegenden Streifen vertieft, die eruegert:
Zwischenriume glatt unregelmiissig einreihig punk-
tiert, die Punkte viel kleiner als diejenigen in den Streifen; der tiefe
Bindruck am Fliigeldecken-Absturz kreisf6rmig, innen ausgeschnitten
und am Rande mit stumpfen Zahne jederseits versehen,
Suturalecken der Fliigeldecken stumpfwinkelig.
Weibchen. Blass gelblich; die Stirn grob punktiert,
die Mittellinie kurz; Halsschild ziemlich dicht fein
punktiert, hinten neben der Mittellinie je ein grosser
halbovaler Punktflecken, bestehend aus sehr zahlreichen yg. Platypus
ausserst kleinen Punkten; die Fliigeldecken mit Punkt- TEIOCHEES Sore Be
. . : . . puis. epres-
streifen, die Punkte kleiner als beim ¢ und wenig ver- ain @ mens
tieft, die Suturalstreifen vertieft, die Zwischenriume WO mestien. ik
2 ae9 : 2 xX vergrossert.
sparsam einreihig fein punktiert.
Diese Art gehort in die Niihe von Platypus lepidus Chapuis und Pl.
caliculus Chap. ; unterscheidet sich jedoch von beiden Arten leicht durch
die Form des Ausschnittes am Fliigeldecken-Absturze (Fig. 7 u. 8).
In meiner Sammlung befinden sich genau gleiche Exemplare von der
Insel Sumatra.
ILLUSTRATIONEN.
TAarer I.
Yakal-Rinde mit Frassfigur von Spherotrypes philippinensis Strohmeyer.
TEXTFIGUREN.
Fic. 1 und 2. Spherotrypes philippinensis Strohmeyer. Mentum, palpi labiales et
3.
maxillae. 80X vergréssert.
Cryphalus squamulosus Strohmeyer. Antenna. 125 vergréssert.
4-6. Ozopemon laevis Strohmeyer.
4. Antenna (scapus et funiculus).
5. Mentum (palpi labiales et ligula).
6.
7. Platypus schultzei Strohmeyer. Depressio et marginatio postica. 15X
Maxilla.
vergrossert.
. Platypus lepidus Chapuis. Depressio et marginatio postica. 15x ver-
grossert.
29
pe shea
nr |
STROHMEYE
BORENKAFER DER PHILIPPINEN. | [Pnim. Journ. Scr., Vou. VI, No. 1:
THE PHILIPPINE JOURNAL OF SCIENCE,
D. General Biology, Ethnology and Anthropology.
Vol. VI, No. 1, February, 1911.
NOTES ON THE DIGESTIVE SYSTEM OF HYDROCORAX.
By Hotton C. Curt.
(Surgeon, United States Navy.)
Because of their peculiar appearance and strange habits, the hornbills
have always been of popular and scientific interest, and a very large
number of articles have been written about them.
Their method of nesting, mode of flight, and gross anatomy have been
abundantly described, while some fairly good accounts of their habits
have been given.*
In order to try to learn something regarding the periodical casting-off
of the lining of the stomach, as described first by Bartlett,? I have recently
made a series of histological sections of the various parts of the gastro-
intestinal tract of Hydrocorax hydrocorax (Linneus), and find facts of
sufficient interest to record.
The best results are obtained by taking small portions of tissue from
a recently collected bird and placing them in a 10 per cent aquous
formalin solution for eighteen hours; from this, the tissue is transferred
to 70 per cent alcohol, where it is kept until ready to use.
Within a few days one may embed the tissues in parafine, cut
moderately thin sections, and stain by the Van Gieson or by the hema-
toxylin and eosin method. The Van Gieson stain has the very desirable
quality of giving a perfect differentiation. Muscle stains yellow, con-
nective tissue stains red, and colloid tissue stains orange.
By this stam, the muscular coat can readily be separated from the
mucous and serous coats, while by its nuclear staiming the cells are well-
defined and add to the clearness of the picture.
Before giving a description of the sections, I wish to call attention to
several statements, found in standard books, regarding hornbills and
which I do not find to correspond with my examinations and observations
of Hydrocoraa hydrocorar. For example, Newton * says that the “horn-
* Newton, Dictionary of Birds, London (1893), 432-437.
2 Proc. Zool. Soc. London (1869), 142-146.
5 Loc. cit.
31
32 : CURL.
bill, at least in captivity, never has any fat about him.” The species
mentioned is often found to be extremely fat and it takes a long time
to remove the thick layer from the skin, while the abdomen contains fat
in quantities. In other specimens collected under similar conditions,
very little fat is present. Again, the statement that the large hornbills
make so much noise when flying that they “can be heard a mile,” does
not apply to the bird mentioned.
The most important thing which my findings tend to show to be in
error, is regarding the muscular layers of the intestine. Authorities
make the general statement that the circular layer of the intestine is
found eaternal to the longitudinal layer, as in the cesophagus. This is
true in some birds, but in many it is by no means so. In Hydrocoraz,
in @Mtheopsar, in Anas, and in Bubulcus, the Van Gieson stain shows
clearly that the intestine has an outer longitudinal layer of muscle in
contact with the peritoneum; next, internal to this, a circular layer
and still more internally, a thinner longitudinal layer, with some oblique
fibers and intimately blended with the submucosa. This last layer of
muscle corresponds very closely to the muscularis mucose In mammals
and is sometimes so developed as to become a fairly thick longitudinal
layer. These layers are shown very clearly in the photomicrograph of
the intestine of Hydrocorax hydrocorar. Anyone familiar with histo-
logical technique can verify the above in the genera mentioned, and I
dare say in many others by using a two-thirds inch objective for routine
and one-sixth inch for occasional differentiating.
In the following descriptions of the parts of the alimentary tract,
the measurements given are from alcoholic specimens, previously run
through the 10 per cent formalin and are slightly less than those from
fresh material. The cesophagus, proventriculus, stomach, and intestine
are described and photomicrographs given to show the histology.
The cesophagus is 200 millimeters in length and will admit the thumb
when fully dilated; at the lower end it becomes funnel-shaped and
increases in size as it reaches the proventriculus. The mucous mem-
brane is thrown into longitudinal corrugations which run unbroken for
almost the entire length; these corrugations project further into the
lumen in front than behind throughout the upper three-fourths; in the
lower fourth, they are of about equal size on all sides. Dilatation of
the cesophagus does not obliterate them and the best-developed ones
measure 2 millimeters in height.
A cross section shows microscopically that there is an external, circular,
muscular layer; next, an internal, longitudinal layer intimately connected
with the mucosa, in fact projecting inward into the bases of the ruge.
The mucous membrane being thrown into longitudinal corrugations,
a cross section gives a circle of inward projections with connective tissue
frame work, the usual blood vessels, and covered with epithelium. A
layer of globular cells lies beneath the epithelium and each opens by a
DIGESTIVE SYSTEM OF HYDROCORAX, 33
short duct on the free surface of the membrane. The deeper cells of
the epithelium show round nuclei; these become flatter toward the free
inner surface, and at the surface they are almost as flat as those seen in
the skin. Apparently only simple mucus for lubrication is secreted by
the lining of the esophagus. The photomicrograph shows the structures
quite well.
The proventriculus is 30 millimeters in length and the wall is 8
millimeters thick in the thickest part, just above the sphincter muscle
which lies between it and the stomach. 'The inner surface is thickly set
with the mouths of glands and when examined in a recently collected
bird, is covered with a thick coat of sticky, mucoid material. On section,
an outer fibrous coat is seen; next a strong, circular, muscular layer;
then a longitudinal, muscular layer on which rests a layer of glands
beneath the mucosa. The glands of this layer are large, each is inclosed
in a connective tissue capsule and, somewhat like a salivary gland,
presents a radiating, tubular structure with a central space in which there
are very few cells and which is filled with mucoid material. Hach gland
(or at least those of the inner layers), opens on the free surface of the
mucous membrane by a wide mouth, which passes through the mucosa
proper. They resemble “Brunner’s” glands in that they lie below the
muscularis mucose. Internal to this glandular layer is the mucosa
proper, of ordinary type, with villi projecting from the surface and with
a network of muscle fibers, forming a true, reticulate muscularis maucose.
It is evident that the glandular layer of the proventriculus is a highly
specialized structure, undoubtedly supplying the essential digestive fluid
for this part of the tract. his is the more certain when we remember
that the tough, deciduous membrane of the stomach, about to be described,
would effectively prevent any digestive fluid which might be secreted by
the glands of the stomach from coming in contact with the food.
The stomach of this large hornbill when empty, is oval with flattened
sides and varies in thickness from 2 millimeters on the membranous
sides, to 11 millimeters where the muscle is thickest. The muscle fibers
eross in a radiating manner from one tendinous disk to the similar disk
on the other side, and are reinforced by numerous other fibers arising
from the membranous, internal muscle-sheath. There is the usual
modification of fibers at the cardiac and pyloric openings and at the
cardiac opening a round, cord-like, circular muscle, 5 millimeters in
diameter, acts as a strong sphincter between the proventriculus and
stomach. At the pyloric opening the sphincter is less well-marked.
The entire lining of the stomach is corrugated and presents a brownish,
irregular surface. On section this is seen to be due to the deciduous”
membrane which, depending on its stage of development, is’ more or
less loosely attached to the stomach proper. The cardiac and pyloric
openings are but 15 millimeters apart. As the entire organ when empty
1010963
34 CURL.
is 50 millimeters in diameter, and when filled with food twice as
large, it can readily be seen that when the lining membrane is cast off
entire, it forms a sac with
the two openings close to-
gether at the top.
In a stomach where the
sac-like lining is about to be
cast off, it separates from
the entire surface of the
stomach before its upper,
neck-like portion separates
finally around the pyloric
opening, at which point it
thins down rapidly and dis-
appears just above the
sphincter muscle. On the
other hand, in a specimen
where the lining membrane
Fic. 1.—Stomach of Hydrocorax hydrocoraxz show-
ing: A, deciduous membrane almost
ready to be cast off (note its separa- is im an earlier stage of for-
tion) ; B, stomach before the prepara-
tory separation has taken place. mation (a. €., Soon after the
last one has been cast off),
no macroscopical separation can be demonstrated, although microscop-
ically the line of future separation is well seen.
On section the stomach is found to have an external serous coat, a
thick muscular coat, and a mucous lining. There is nothing peculiar
about the serous and muscular layers. The mucous membrane shows
closely studded, long, finger-like villi which have tubular glands at their
bases and are covered by a single layer of cells with large nuclei.
When the deciduous membrane is just beginning to form, the spaces
between the villi are filled with colloid-appearing material which stains
a bright orange-yellow by the Van Gieson method. A little later this
layer becomes thicker and lies as a continuous coat over the entire inside
of the stomach. Before it is ready to be thrown off, it becomes in fact,
thicker than the mucosa itself. The deciduous membrane is of homo-
geneous structure, is quite tough, and on its mucous-membrane side is
an accurate cast of the ruge of the stomach. It seems certain that this
layer, which is so peculiarly cast off, is formed by secretion from the
glands of the stomach and after reaching its full thickness, separates
spontaneously, leaving the glands to begin at once the formation of a
new sac.
The intestine is from 920 to 950 millimeters in length and, having
no cecum, is not clearly divisible into large and small portions except
possibly by its structure when examined from within. The mucous
DIGESTIVE SYSTEM OF HYDROCORAX. 35
membrane of the upper three-fourths has a velvet-like feel and shows
long villi lying close together. At a point about 250 millimeters from
the rectum and about where one would expect to find the cea, if such
did exist, there is a short section of the gut which is dilated, has thin
walls, and an entirely different type of villi. his section is about 70
millimeters in length, and below it one again finds villi of the same
type as occur in the upper intestine.
The intestine differs from the cesophagus in the position of the mus-
cular layers. A section shows externally the serous coat, made up of
connective tissue; next to this a well-developed longitudinal muscular
coat ; next, internal to this, the circular muscular layer. The muscularis
mucose lies internal to this circular layer and then comes the mucosa
with its epithelial lining. This is shown perfectly in the cross-section
of the gut where the outer longitudinal fibers are seen cut across and
the circular fibers are seen in their circular plane. Simple alveolar
glands lie at the base of the villi.
After this brief description of the digestive tract, the following points
appear worth considering: I have collected three large hornbills at
practically the same time, months after the breeding season was over, and
found the deciduous membrane in three different stages of development ;
one was separated entirely from the stomach except for a narrow zone
around the cardiac opening, one was just beginning to form, and the
third was in an intermediate stage. At other seasons the same has been
found and in some, the sac, ready to be cast off, was packed full of
indigestible parts of the fruit on which the birds were feeding. It seems
reasonable to suppose that, at least when the breeding season is past,
the food, mixed with, and acted upon by, the secretion of the pro-
ventricular glands, passes into the deciduous sac lining the stomach ; here
muscular action completes the mixing, triturates the food, and prepares
the digestible parts to pass over into the duodenum. ‘The refuse is then
periodically ejected in the membranous sac. Whether this routine is
changed at the breeding season, I can not say.
Another point of interest is the abrupt change in the character of the
mucous membrane in the short section of the gut at about the point one
would expect to find ceca; this, together with the dilitation and thinning
of the intestinal wall at this point may suggest the explanation of the
absence of ceca in certain species where the diet is similar to that of
others in which these organs are present. Is it not possible that the
mucous membrane of the gut itself takes on, in these specialized areas,
the functions performed by the ceca in other birds? In Bubulcus for
example, where the bud-like, single cecum is very short, the mucous
membrane of the adjacent gut contains numerous masses of lymphoid
tissue, from 90 to 250 millimeters in diameter, not found in other parts
36 CURL.
of the intestine, but found in the cecal bud itself. As we know, in many
animals where there is no appendix, the head of the cecum contains a
great increase of lymphoid tissue.
Numerous interesting superstitions and beliefs concerning the calao,
or great Philippine hornbill, are found among the natives and are worth
collecting, while a systematic and accurate study of the bird’s habits
would well repay the observer.
ILLUSTRATIONS.
Prate I.
Fic. 1. Cross section of esophagus of Hydrocorax hydrocoracz.
2. Longitudinal section of proventriculus of Hydrocorax hydrocorax: A,
Mucous membrane; B, muscularis mucosae; C, specialized glands; D,
muscular coats.
PuatTe II.
Fic. 3. Section of stomach of Hydrocorax hydrocorax: A, Deciduous membrane;
B, mucosa; C, muscular coats; D, peritoneum.
4. Cross section of intestine of Hydrocorax hydrocorax: A, Peritoneum; B,
longitudinal layer of muscle; C. circular layer of muscle; D, muscularis
mucose beneath the mucosa.
TEXT FIGURE.
Fig. 1. Stomach of Hydrocorax hydrocoraz showing: A, deciduous membrane
almost ready to be cast off (note its separation); B, stomach before
the preparatory separation has taken place.
37
CurL: DIGESTIVE SYSTEM OF THYDROCORAN, | {Piis. Journ. Ser, Vou. VI, No. 1,
ah) .
CURL:
DIGESTIVE SYSTHPM OF HYDROCORAX. |
Fic. 3.
(Putt. Journ. Scr., Vou. VI, No. 1.
THE PHILIPPINE JOURNAL OF SCIPNCE,
D. Generai Biology, Ethnology and Anthropology.
Vol. V1, No. 1, February, 1911.
NOTES ON A COLLECTION OF BIRDS FROM NORTHERN
NEGROS.
By Ricuarp C. McGrecor,
(From the Ornithological Section, Biological Laboratory, Bureaw of Science,
Manila, P. I.)
The earliest paper on the birds of Negros that I have seen is one by
Walden and Layard? on a collection made in the southern part of the
island by Mr. L. C. Layard. Of the seventeen species there recorded
three are described as new. In 1875 Walden published his monograph,
“A List of the Birds Known to Inhabit the Philippine Archipelago,”
including therein some species obtained in Negros by the German col-
lector Meyer, and giving the total number of species known from the
island as thirty-eight. Two years later, Mr. A. H. Everett began his
explorations in the Philippine Islands which resulted in the discovery
of the many new species of Philippine birds described and figured by
Tweeddale in the Proceedings of the Zodlogical Society of London,
1877-1879. LEverett* collected at Valencia and Dumaguete in the
southern part of the island and secured specimens of fifty-six species;
twenty-four of these had not previously been recorded from Negros and
six of them had not been known from the Philippines. Dasycrotapha
speciosa, the most remarkable of the three new species discovered by
Hyverett, was described and figured in a separate paper.*
In 1874 Steere began his work in the Philippine Islands, visiting
Negros during the next year, where he obtained specimens of thirty-eight
species of birds, among them being the following new species which were
described by Sharpe.°
Oriolus steert, Diceum hematostictum, Mthopyga magnifica, Anth-
reptes chlorigaster, and Phapitreron nigrorum.
As a result of the collections made by the Steere Expedition,® eighty-
one species were recorded from Negros. Two species, Cryptolopha
1[bis (1872), 93-107, pls. 4-6.
2?Trams. Zool. Soc. London (1875), 9, 125-252, 23-34.
3 Proc. Zool. Soc. London (1878), 280-288.
* Proc. Zool. Soc. London (1878), 114, pl. 9.
5 Nature (1876), 14, 297, 298; Trans. Linn. Soc. London, 2d. ser. Zool. (1877),
307-355, pls. 46-54.
*A list of the birds and mammals collected by the Steere Expedition to the
Philippines, Ann Arbor, 1890.
; 39
40 : M’GREGOR.
nigrorum and Abrornis olivacea, collected by the Steere Expedition were
described and figured by Moseley.”
Bourns and Worcester * added twenty-four species to the Negros list
and described the following as new: Phapitreron maculipectus, Batra-
chostomus menagei, Ceya nigrirostris, Oriolus nigrostriatus (= steeri),
Aithopyga bomta, Hyloterpe winchelli, and Rhinomyias albigularis.
Grant’s ° report on Whitehead’s collection includes notes on eighty-six
species, three being described as new: Turdus nigrorum, Brachypteryx
brunneiceps, and Cittocincla nigrorwm.
In 1894 Clarke began a series of papers based upon birds collected in
Negros by W. A. Keay.t° In these papers eighty-six species are recorded
and one new species, Phloganas keayi, is described and figured.
In February and March, 1909, Mr. Andres Celestino made collections
in the vicinity of Cadiz, northern Negros, and the species obtained by
him are listed in the present paper. The following species are believed
to be here recorded from this island for the first time: Astur trivirgatus,
Tachorms pallidior, Cyanomyias celestis, and Aithopyga bonita.
LIST OF SPECIES.
TRERONIDAZ.
Osmotreron axillaris (Bonaparte) .
One female.
Phapitreron maculipectus Bourns and Worcester.
The collection contains nine specimens of this rare dove. The collector
gives the length as 280 to 292 millimeters; eyes brown; bill black; feet
red ; nails brown.
Measurements of Phapitreron maculipectus.
Culmen
Sex. Wing. | Tail. | from | Tarsus.
base.
mm. mm. mm. mm.
145 118 24 21
143 120 23 20
145 118 24.5 20
141 114 27 18
DOs 2 see ee ee ee eee 147 120 24 19
149 119 23 19
140 112 23 18
145 118 22 18
137 102 22 19
® This specimen is in poor plumage.
TIbis (1891), 46, 47, pl. 2.
5 Minnesota Acad. Nat. Sci. Occ. Papers (1894), 1, 1-64.
°Tbis (1896), 325-565.
This (1894), 532-535; Second Contribution, bid. (1895), 473-479; Part Ill,
Tbid. (1898), 119-124; Part IV, Ibid. (1900), 351-361, pl. 8.
BIRDS FROM NORTHERN NEGROS.-— - 41
Phapitreron nigrorum Sharpe.
Three males and one female.
Leucotreron occipitalis (Bonaparte) .
Two males in fine, adult plumage. This yellow-breasted fruit pigeon
was taken in Negros by Whitehead also.
Muscadivores chalybura (Bonaparte).
One specimen.
Zonophaps poliocephala (Hartlaub).
One pair in fine adult plumage.
COLUMBIDA.
Columba griseogularis (Walden and Layard).
Two females. Some individuals of this species from Batan, Batanes,
have the bills considerably longer than the Negros examples, but the
difference is not constant.
ARDEIDA.
Bubulcus coromandus (Boddaert) .
One female in winter plumage.
FALCONIDA.
Astur trivirgatus (Temminck).
One specimen, an immature male. This species has not, so far, been
recorded from Negros.
Spilornis panayensis Steere.
One adult male in good plumage.
PSITTACIDA.
Prioniturus discurus (Vieillot).
A pair, taken February 24, and a female, taken March 10, are in fine
plumage.
Tanygnathus lucionensis (Linnus).
Two adult males; in one specimen the blue of the crown and nape
is unusually dark.
Loriculus regulus Souancé.
One male and three females of the central island colasisi were collected ;
the male is in immature plumage.
ALCEDINIDA. ®
Ceyx bournsi Steere.
The only specimen, a female, of Bourns’s kingfisher in this collection
has a considerable quantity of black mixed with the deep blue of the upper
surface.
4? M’GREGOR.
Halcyon moseleyi (Steere).
One female specimen of this very rare kingfisher was collected on
February 19. Wing, 108 millimiters; tail, 86; culmen from base, 46;
tarsus, 15. Length, taken by the collector, 265 millimeters.
BUCEROTIDAZ.
Penelopides panini (Boddaert).
One pair of the Panay tarictic.
Craniorrhinus waldeni Sharpe.
Three males and two females of Walden’s hornbill, all in good plumage.
HEMIPROCNIIDA.
Hemiprocne major (Hartert).
One male specimen ; wing, 141 millimeters.
MICROPODIDZ.
Tachornis pallidior McGregor.
One specimen, without sex mark, was collected on March 10. This
is the first record of the species.
CUCULIDA.
Surniculus velutinus Sharpe.
In an adult female from Cadiz most of the rectrices are conspicuously
bordered with white and several of the longer upper tail-coverts are
faintly tipped with the same color. This species was taken in Negros
by Whitehead also.
Hierococcyx sparverioides (Vigors).
>
Two males in adult plumage.
Cacomantis merulinus (Scopoli).
One male specimen.
CAPITONIDA.
Xantholama roseum (Dumont).
Two specimens, male and female.
PICIDA.
Yungipicus maculatus (Scopoli).
‘
Four males and one female were taken in February.
Chrysocolaptes xanthocephalus Walden and Layard.
One male and one female in good plumage.
Thriponax hargitti sifarpe.
Thriponaz hargitti Clarke, Ibis (1895), 475-477; McGregor, Man. Phil. Bds.
(1909), 1, 409.
This collection contains three males and four females of Hargiti’s
black woodpecker ; all of them are in good plumage and well prepared.
BIRDS FROM NORTHERN NEGROS. 43
In five specimens there is a wide, buffy white band across the rump, in
one male the white band in narrow, and in one female most of the back
and uropygium are bare. ‘The lower mandible in all these Negros speci-
mens is whitish. The Masbate and Negros birds appear to be of the
same species and they must be called 7’. hargitti unless Steere’s 7. philip-
pinensis can be shown to be distinct from the Thriponax of Palawan.
PITTIDA.
Pitta erythrogastra Temminck.
One female.
HIRUNDINIDA.
Hirundo rustica Linnzus.
One female swallow, taken March 17, differs from the other specimens
from Negros in haying the pectoral band continuous across the fore breast
and in haying the white of the under surface distinctly washed with
pale ochreous-pink.
Hirundo gutturalis Scopoli.
One female and two male swallows, March 17, are of the eastern
species.
MUSCICAPIDA..
Cyanomyias ccelestis (Tweeddale) .
The celestial-blue flycatcher is represented in the present collection
by an adult female. ‘There appears to be no previous record of this
species for Negros.
Rhipidura albiventris (Sharpe).
Three specimens of the white-bellied fantail.
Xeocephus rufus (Gray).
Two males and one female.
Cryptolopha olivacea (Moseley).
Two specimens of the olivaceous flycatcher warbler.
CAMPOPHAGID~-.
Artamides panayensis Steere.
Two males and one female.
Edolisoma panayense Steere.
This very distinct and handsome cuckoo shrike is represented in the
present collection by eight males and six females.
PYCNONOTIDA.
lole guimarasensis Steere.
Two males and one female.
—— ESS ES
44 M’GREGOR.
TIMELIIDA.
>
Dasycrotapha speciosa Tweeddale.
The type of this curious species was collected by A. H. Everett at
Valencia in southern Negros and was described and figured by Tweeddale
in the Proceedings of the Zodlogical Society of London for 1878. Other
specimens were secured in Negros by the Steere Expedition and by the
Menage Expedition. The collection now under consideration contains
a series of seven males and one female. The sexes appear to be similar
in color. The structure of the feathers is very similar to that found in
the various species of Mixornis and Macronous, but the feathers of the
lower back are not noticeably lengthened, while the orange-colored
feathers above and behind the eyes are stiff and harsh. The length of
specimens in the flesh, as given by the collector, is from 145 to 150 milli-
meters.
Measurements of four males and one female are given herewith.
Measurements of Dasycrotapha speciosa.
Culmen| Bill
Sex. Wing. | Tail. | from | from | Tarsus.
base. | nostril.
mm. mm. mm. mm. mm.
Malew. 2 a ee 67 56 16 10.5} 18.5
Do S22 2-2 ss ee Ee 70 58.5 17 11 19
DO jose ee 68 56 17 11 18
DO jsa8 22k sate cat ee eee 68 59 16 11 17
Kemales =~ = See 65 53 15 10 18
TURDIDA.
Kittacincla superciliaris Bourns and Worcester.
Cittocincla nigrorum Grant, Ibis (1896), 547.
Upon comparison of an adult male shama from Negros with adult
males from Ticao and Masbate, the characters given for Cvttocincla
nigrorum do not appear to be valid. In the first place the superciliary
stripe in all three species is practically of the same width. In K. luzon-
iensis alone the stripes are connected across the forehead. This species
is also distinguished by the rusty brown rump, large white spots on
rectrices, and other characters. In K. swperciliaris the spots on the
rectrices are much reduced or may be altogether obliterated. The length
of tarsus in the original description of K. swperciliaris is clearly a
mistake. :
A specimen from Cadiz, Negros, marked female, differs from the
male as follows: The superciliary stripes are continued forward above
the lores to the base of bill; the upper parts are less glossy;the chin and
throat are white and there is a narrow band of black across-the.chest.
EE a |
BIRDS FROM NORTHERN NEGROS. 45
Measurements of Kittacinela.
Cul-
Species. Sex. Wing. | Tail. | pe Tarsus.
|
base.
mm, mm. mm. mm,
TAZ ONVENSES = on on ea en 82 82 18 26
80 73 19 26
83 74 19.5 | 27
79 66) 18 25
78 fil) ilz/ 27
DO eee ee ea ne Female___ 74 67 17.5] 26.5
Pratincola caprata (Linneus).
One male and one female.
SYLVIIDA.
Megalurus tweeddalei McGregor.
One specimen.
LANIIDA:.
Hyloterpe winchelli TRONS and Worcester.
Three males and two females.
PARIDA.
Pardaliparus elegans (Lesson).
One male, March 19, and one female, January 29, from Cadiz, do not
differ from specimens taken in Bataan Province, Luzon.
SITTIDA.
Callisitta cenochlamys (Sharpe).
One male and two females.
CERTHIIDA.
Rhabdornis mystacalis (Temminck).
A male, the only specimen of Rhabdornis in the present collection,
differs from specimens taken in Luzon in haying the bill conspicuously
longer, the feet larger, and the color of the back and rump darker. If
additional specimens from Negros shovy, that these characters are constant,
the species may be known as Rhabdornis longirostris.
ZOSTEROPIDA.
Zosterops nigrorum Tweeddale.
Two specimens; one of these is slightly albinistic, having five rectrices
white, washed with pale yellowish green.
I have long suspected that a series of birds of this genus, collected
by me on the little island of Cresta de Gallo, represented a distinct
species. With topotypes of Zosterops ngrorum at hand I still hesitate
to separate the Cresta de Gallo individuals as a species, although in the
latter the wing, tail, and bill average longer and the color of the upper
parts is more uniform and more yellowish.
46 M’GREGOR.
Measurements of Zosterops nigrorum.
Cul-
Locality. Wing. | Tail. fon ‘Tarsus.
base.
mm. mm. mm. mm.
Negros=22-) 3 eee 54 42 12.5.) 15
Dom | 55 38 12 16
Masbate’ 214 2S - a eae ee eee 52 36.5 13 15.5
Micsor==_ =f —s =e 806 38 13 16
Cresta de Gallo__ wae lee DS 44 14 17
Doles ee 58 44 14 18
DO: oa set se Se eee 57.5 43 13.5 | 17
DO w22 Sa fees k aan ss ee 56.5 43 14.5 | 16
DICAEIDA.
Diczeum hzematostictum Sharpe.
Three males and two females.
Diczeum dorsale Sharpe.
Four males and one female in fresh plumage.
NECTARINIIDA.
AEthopyga magnifica Sharpe.
One adult male; the types of this species were collected in Negros.
A=thopyga bonita Bourns and Worcester.
Two full-plumaged males from Negros differ in no way from a male
from Ticao and a male from Cebu. This appears to be the first record
of the Visayan sunbird from the Island of Negros.
Cinnyris guimarasensis Steere.
One male and two females of this species were taken in March.
MOTACILIIDA.
Anthus rufulus (Vieillot).
One specimen, January 29.
PLOCEIDA.
Munia jagori Martens.
Two specimens.
Uroloncha everetti (Tweeddale).
One specimen, February 4.
ORIOLIDA=
Oriolus steeri Sharpe.
Thirteen males and six females.
DICRURIDA.
Dicrurus mirabilis Walden and Layard.
Two males.
THE PHILIPPINE JOURNAL OF SCIENCE,
D. General Biology, Ethnology and Anthropology.
Vol. VI, No. 1, February, 1911.
ON A QUINARY NOTATION AMONG THE ILONGOTS OF
NORTHERN LUZON.
By Orro ScneeReR.
Within the area of Austronesian languages there are represented, in
a pure or in a modified form, all those systems of numeration which are
designated as quinary, decimal, or vigesimal notations, according as
they are based upon the counting of tke digits of only one hand, of both
hands, or of both hands and feet.
From the Philippines in particular none but decimal systems have
hitherto been recorded, not excepting such tribes as the Negritos,
Tagbanwas and similar people of low culture.*
In view of this general use of decimal series of numerals in the Phil-
ippines it will be of interest here to make known a case of quinary
notation in northern Luzon as found by me some time ago in an old
Kgongot (i. e., Llongot) catechism dating from 1792, and declared by its
authors, three Spanish missionaries, to be a revision of a still older text.?
As is to be supposed, the catechism does not give the Egongot numerals
by way of demonstration. They occur in the text mostly im the form
of ordinals in such places as “The ten commandments,” “The articles of
faith,” and the like. Collecting these ordinals I obtain the following list:
Ta onbucoug the first - Ta catambiang no siyet the sixth
Ta cadua the second Ta catambiang no dua the seventh
Ta catgo the third Ta catambiang notgo the eighth
Ta caapat the fourth Ta catambiang no apat the ninth
Ta catambiang the fifth Ta catampopoo the tenth
1 For a full treatise on the numerals of these systems see the praiseworthy
paper of Professor Frank R. Blake in Journ. Am. Or. Soc. (1907), 28: Contribu-
tions to Comparative Philippine Grammar, Part II.
2“Catecismo de doctrina cristiana en Egongot, escrito por el M. R. P. Fray
Franciseo de la Zarza, O. S. F. Dado 4 luz por Fernando Blumentritt, ... y
aumentado por el mismo editor con equivalencias del texto egongot 6 ilongote
en castellano, tagalog y moro de Maguindanao.” (Vienna, 1893). As will
be shown, the form “Egongot” for “Ilongot” represents an idiomatic pronunciation
of this word among at least that section of the Ilongots whose dialect is used
in this catechism. For this reason it is employed by me in this paper as a term
distinctive for that dialect.
47
48 SCHEERER.
Ta, appearing before each of these numerals, is an Egongot demon-
strative particle acting as article.
Onbucoug is the equivalent, not of “one,” but of “first.’? The word
occurs, in this or related forms, in several other passages. There is
evidently a typographical confusion between “w” and “n.” - Compare—
Na mucong toi Dios Ama, ta Dios Anac, at ta Spiritu Santo?
Is first (superior) the God Father to God Son and to Ghost Holy?
Auan-a namucoug, auan-a naonod de, ten sisiet ta enca Dios de.
There is not being first, there is not following behind among them, for only one
the Godship their.*
Ca in cadua, catgo, etc., is a prefix making ordinals from cardinals, not
only in Egongot but in several other dialects of Luzon.
Eliminating these three factors from the above list, and observing the
composition of the numerals from “six” to “ten,” we have all the necessary
material for establishing the following list of Egongot cardinals:
wee Egongot. Pangasinan. pee Egongot. Pangasinan.
one siyet (sitet) isa six tambiang no siyet | anem
two dua dua seven | tambiang no dua | pito
three | tego talo eight | tambiang notgo ualo
four apat apat nine tambiang no apat | stam
five tambiang lima ten tampo (tampoo) sampolo (samplo)
The cardinals tego, tambiang, and tampo (tampoo) occur as such re-
peatedly in the text; siet was quoted above in its restrictive form sistet.
For comparison with a series of typical Philippine numerals the cor-
responding Pangasinan cardinals have been added.
“One” is expressed in Hgongot by a word, sitet or siyet, which, compared
with Pangasinan as well as with any other Philippine dialect, shows
hardly any affinity, at least not prima facte.
From “two” to “four” Egongot uses numerals which, though varying in
form, are the common property of all these dialects. The characteristic
variation in the case of the numeral “three” in Hgongot is the change
from general Philippine / or d to g. ‘The same change, typical for Hgon-
got, is seen in such other words as gema, “hand” (Tagalog lima), gake,
“male” (Tag. lalaki), uge, “again,” “anew” (Tag. ult), etc. It is this
sound-change which accounts also for the form “Egongot” instead of
“Tlongot,” the change from 7 to e being the ordinary fluctuation of these
vowels.
“Five” is expressed, not by Jima, in which all Philippine dialects agree,
and which, as we have just seen, would be here gema, but by the idiomatic
term tambiang, formed of a prefix tam (cf. tampo) before a stem, biang.
* Op. cit., p. 19.
QUINARY NOTATION AMONG THE ILONGOTS. 49
From “six” to “nine” the Egongot numerals are clearly seen to express
“five and one,” “five and two,” “five and three,’ and “five and four,”
which shows that, once “five” is reached by counting the fingers of one
hand, the count is begun anew. That the particle no is the equivalent
of “and,” is proved by a phrase of the text: dit bucolot no nauguin
binimiaguen, “the pagans and bad Christians.” 4
The numeral for “ten” is tampo, evidently with long o (compare
the variant tampoo). It consists of the prefix tang, which also appears in
tambiang, changed to tam- by the influence of the labial that follows, and
stem po or poo, which is the common Philippine polo or pulo with elision
of 1.
For the two numerals “one” and “five,” in Egongot we find no imme-
diate correspondent among the forms of the equivalent numerals in the
generality of the other dialects. But apart from these two words we have
as characteristic of this series of Hgongot numerals that it is based on
a clearly quinary plan, and that the words used are for the greater part
the common property of a family of languages which, as far as it is
represented in the Philippines, uses none but decimal systems. Similar
cases of quinary series we find in Formosa.®
It remains to be pointed out that, although the Hgongot plan is
quinary, as far as I have been able to illustrate it above, it is only im-
perfectly so. Ifit were purely quinary the numeral for “ten,” instead of
being expressed by a distinct word, would be given by such a term as
“five-five” or “two-fives.” Again, beyond “ten,” the advance would be
by fives, not by tens. But this is a question not to be decided from the
text before me, which lacks examples of higher numerals. I may, how-
ever, add that there exists a variant of the Egongot speech here illustrated,
the speakers of which use a purely decimal series from “one” to “ten,”
and it may be believed that this will ultimately supersede the quinary
series. or the present it must suffice that evidence has been given here
of the existence in the Philippines of a representative of the quinary nota-
tion which is generally assumed to be a more primitive form of counting
than the decimal system.
“Op. cit., p. 27.
° Cf. the numerals given under ‘Pep. Paz.’ and ‘Shek. T.’ in Table I of The
Batan Dialect as a Member of the Philippine Group of Languages. Division of
Ethnology Publications, Manila (1908), 5, pt. I.
101096 4
y
ie pipe sie
wich eae od =
- ‘ag ee 9 er ce
> teased ta eat ganget rb Ss
i ‘es Bi er wv) geet: Sasi =
fo: ESE ii ‘aki Gai | ty
_ py
- Bask
f z
REVIEW.
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Vou. VI APRIL, 1911 No. 2
LES FORAMINIFERES DANS LE TERTIAIRE DES PHILIPPINES.
Par le Professeur Henri DovuviLyis.
(Scole Nationale Supérieure des Mines, Paris.)
SOMMATRE.
I. AVANT-PROPOS.
II. DESCRIPTION DES ESPECES:
Alveolinella Cycloclypeus communis
Orbitolites martini Rotalia
Opereulina costata Polystomella
Heterostegina Nummulites subniasi sp. nov.
LepipocycLina (Revision de ce genre. Sections Hulepidina et Nephrolepidina:
1. L, sumatrensis 13. L. martini Schlumb,
2. L. carteri 14. L. formosa
3. L. gigantea 15. L, angularis
4. L. radiata 16. L. joffrei
5. L. multipartita 17. L. gallienii
6. L. verbeeki 18. L. richthofeni
7. L. neodispansa 19. L. martini Smith
8. L. insule-natalis 20. L. provalei
9. L. ephippioides 21, L. ferreroi
10. L. murrayana 22. L. tournoueri var. angulosa
11. L. andrewsiana 23. L. tournoueri var. inflata
12. L, ngembaki 24. L. tournoueri var, borneénsis)
DESCRIPTION DES ESPEcES:
_ L. insule-natalis L. inflata
L. richthofeni L. ef. marginata
L. formosa Miogypsina irregularis
L. inermis sp. nov. Amphistegina niasi
L. smithi sp. nov. A. ef, mamillata
L. verbeeki
III. R&sumé Er ConcLusions.
101776 53
54 DOUVILLE.
AVANT-PROPOS.
Les explorations géologiques des Philippines et en particulier les
récents travaux de M. Warren D. Smith publiés dans “The Philippine
Journal of Science” ont montré que le Tertiaire de cet archipel était
constitué: 1° 4 la base par un systéme inférieur avec couches de Charbon
exploitées, qui a été attribué a l’Hocene, et 2° par un systeme supérieur
miocéne caractérisé par des calcaires 4 Orbitoides.
L’étude des Foraminiféres qui.m’ont été communiqués par le géologue
précité, permet de préciser cette classification: on peut en effet subdiviser
le systeme supérieur et distinguer 3 séries de couches.
I. Le systéme inférieur lignitifere caractérisé par association des
Nummutlites et des Lépidocyclines.
II. Le systeme moyen caractérisé par V’abondance des grandes Lépido-
cyclines, et la présence des Alvéolines.
III. Le systéme supérieur ot abondent les petites Lépidocyclines et
les Miogypsina.
Cette succession est la méme que celle que l’on observe dans toute
P’Indonésie et en particulier 4 Bornéo,’ ot ces trois divisions corres-
pondent aux couches que j’ai distinguées par les lettres D,—H, F, G,—H.
Elles peuvent étre facilement parallélisées avec les couches de ! Aquitaine.
I. Le systeme inférieur D, partout caractérisé par Vassociation des
Nummulites et des Lépidocyclines, représente le stampren ou Oligocéne
supérieur.”
II. Le systéme moyen H, F, G représente alors les couches de Peyrére
et de St-Géours, c’est-a-dire AQUITANIEN.
III. Le systéme supérieur Hi se rattache complétement par sa faune
aux couches de St-Htienne d’Orthe et surtout 4 celles de St-Paul prés
Dax (Abesse, Mandillot), gisement type du BURDIGALIEN.
Je vais passer en revue les différentes formes que j’ai pu examiner et
je reviendrai en terminant sur les caractéres comparatifs de ces faunes
avec celles des autres parties de l’Indonésie, et celles de l’Hurope.
DESCRIPTION DES ESPECES.
1° FORAMINIFERES IMPERFORES.
ALVEOLINELLA. PI. A, fig. 1.
Ce genre est représenté par une série de moules médiocrement conservés
dans une roche trés tendre, jaunatre, recueillie 4 Sibud Gulch, Old Alpaco
Mines, Cebu, et portant le numéro 273. Cette roche est qualifiée de
marne, mais c’est plutdt un grés tendre avec ciment calcaire peu abondant.
1 Douvillé, H. Les Foraminiféres dans le Tertiaire de Bornéo. Bull. Soc. géol.
France, (1905), VI, 5, 435.
2 Conformément aux travaux les plus récents, la limite entre l’Oligocéne et
le Miocéne, ou entre l’Eogéne et le Néogéne est placée entre le Stampien et
PAquitanien proprement dit.
LES FORAMINIFERES. 55
Elle renferme un grand nombre d’empreintes de Foraminiféres parmi
lesquelles quelques unes sont fusiformes allongées, ayant environ 5 milli-
métres de longueur sur 1 millimétre de diamétre. Elles se rapportent
incontestablement 4 des Alvéolinidés. Sur quelques échantillons il m’a
semblé distinguer sur l’empreinte de la cloison terminale plusieurs ran-
gées Vouvertures. Ces fossiles appartiendraient done au groupe de VAlv.
quoyt, pour lequel j’ai proposé le genre Alveolinella. A ce sujet je ne
puis mieux faire que de citer observation trés intéressante faite par M.
Verbeek: * aprés avoir décrit plusieurs A/veolina des couches 4 Num-
mulites présentant tous wne seule rangée douvertures, il dit quelques
mots de formes rares trouyées dans l’étage inférieur du terrain miocéne,
et il constate qu’elles présentent 3 et méme 4 rangées d’ouvertures les
unes au dessus des autres, “circonstance qui jusqu’a présent n’a jamais
été observée, dit-il, chez des Alvéolines fossiles, mais seulement chez les
espéces vivantes (Alv. Quoyi). Par la, les Alvéolines miocénes se dis-
tinguent nettement des espéces éocenes et oligocénes.” Ces Alveolinella
de Java sont indiquées comme associées 4 de nombreuses Orbitolites dans
un caleaire grisdtre d’4ge miocéne ancien un peu au dessus des grés
quartzeux éocenes. Elles sont un peu plus petites que l’espéce de Cebit,
leur longueur maximum étant de 3.5 millimétres sur une épaisseur de
0.75 millimetre, mais il ne faut pas oublier qu’elles ont été seulement
observées en coupe sur des plaques minces.
Gisement.—Dans les Philippines cette forme est accompagnée par des
Orbitolites, des Operculines et des Polystomelles; les couches qui renfer-
ment cette faune sont riches en Mollusques, parmi lesquels on signale
Dolium costatum. Martin* a eu Voccasion d@étudier un échantillon
d'une marne terreuse tendre provenant de la mine méme d’Alpaco
et riche en coquilles de Lamellibranches et de Gastropodes. C’est
yraisemblablement la méme couche, la différence de couleur prove-
nant de la différence de gisement, les roches jaunes en affleurements
devenant habituellement bleues en profondeur; il signale dans cet
échantillon un fragment de grande Lépidocycline, et en outre Vicarya
callosa. De ces rapprochements il semble qu’on peut conclure que
ces couches sont a la base du systeme moyen et representent l Aquitanien
inférieur, comme A Bornéo et vraisemblablement aussi 4 Java.
Orbitolites martini? Verbeek. Pl. A, fig. 2.
La méme roche jaunatre de Old Alpaco Mine, renferme d’assez nom-
breux moules d’une Orbitolite mince ayant de 5 a 6 millimetres de
diamétre. Sur les empreintes on distingue un grand nombre d’anneaux
concentriques étroits ayant au pourtour environ 0.05 millimétre de lar-
geur, constitués par des moules de logettes ayant 4 peu pres la méme
distance d’axe en axe. C’est exactement la disposition figurée par M.
* Verbeek et Fennema, Description géologique de Java et Madoura (1896), 1141.
* Centralbl. f. Mineral., Geol. wu. Paldon. (1901), 326.
56 DOUVILLE.
Verbeek (Pl. IX, fig. 135). Malheureusement la disposition des loges
en coupe verticale reste bien obscure: la figure 134 de cet auteur indique
pour la forme type 2 rangées d’ouvertures, ce qui placerait cette forme
dans les Sorites; mais c’est seulement un dessin et d’aprés le texte les
coupes ne donnent pas de caractéres précis. Dans les spécimens des
Philippines l’impression du pourtour de la coquille semble indiquer des
ouvertures en rangées plus nombreuses, tandis que les moules de logettes
conservées sur les bases correspondraient peut-étre a une couche super-
ficielle rappelant celle des Marginopora.
Les deux formes sont done incomplétement connues, et leur rappro-
chement n’est que probable.
Gisement.—Dans les Philippines cette forme accompagne les Alveo-
linella, dans des couches qui sont indiquées comme inférieures au Cal-
caire 4 Orbitoides; Aquitanien inferieur.
2° FORAMINIFERES PERFORES.
OPERCULINA.
Les couches du Miocéne des Philippines renferment de nombreuses
Operculines qui paraissent se rapporter 4 2 types un peu différents.
Operculina costata d’Orb. PI. A, fig. 3.
Operculina costata d’Orbigny, Prodrome, étage 26, Falunien B, (1852), n°
2881, 155.
C’est une forme trés voisine de l’Op. complanata et qui s’en distingue
par ce que la surface est ornée de cétes correspondant aux cloisons.
J’en rapproche une forme abondante dans des calcaires tendres jauna-
tres de Minanga river (Cebu, n° 277) ou elle est associée 4 de nombreux
Cyclocypeus communis; elle atteint 7 a 8 millimétres dans son plus grand
diametre et se rattache nettement au groupe de Op. complanata par sa
taille, la largeur du dernier tour et ses cloisons fortement et reguliérement
arquées. Certains échantillons sont presque aussi lisses quwOp. compla-
nata, mais le plus grand nombre est fortement costulé et les costules se
décomposent en granulations plus ou moins nombreuses; elles sont tou-
jours plus accentuées dans le jeune.
Gisement.—D’aprés Vabondance du Cycl. communis dans ces couches,
je les considére comme un peu plus récentes que les calcaires 4 grandes
Lépidocyclines et représentant /’Aquitanien supérieur.
Operculina costata, var. tuberculata. Pl. A, fig. 4.
Je distingue sous ce nom des individus plus petits que les précédents,
attelgnant seulement 4 a 4.5 millimetres; ils sont plus renflés, de section
lenticulaire et présentent de forts tubercules sur les cétes. Ils paraissent
difficiles 4 distinguer des jeunes de l’espéce précédente; peut-étre en re-
présentent-ils seulement la forme A. Ils se distinguent de l’Op. gav-
mardi d’Orbigny, des mers actuelles par leur taille plus grande et leur
forme plus renflée.
LES FORAMINIFERES. 57
Ils se recontrent presque 4 tous les niveaux, mais ils sont surtout
abondants dans les grés tendres de Old Alpaco Mine, ot ils se présentent
a Pétat de moule (éch. n° 273).
HETEROSTEGINA. PI. A, fig. 5.
Les Heterostegina de grande taille ne sont ordinairement pas rares
dans les couches 4 Orbitoides.
J’en ai observé un bel échantillon de 5 millimétres de diamétre fixé
sur une Lepidocyclina insule-natalis du Barrio de Mesaba.
Cycloclypeus communis Martin. Pl. A, fig. 6.
Cycloclypeus communis IX. Martin, Untersuchungen tiber die Organisation von
Cycloclypeus und Orbitoides. Niederland. Arch. f. Zodl. (1880), 5, Pls.
13 et 14.
Carpenter a montré dés 1856 (Pll. Trans. Roy. Soc. London (1856),
146, 547) la constitution de ce genre curieux. C’est en réalité une
Heterostegina dont le développement est devenu annulaire (cyclostégue)
et qui épaissit son test comme Orbitoides, mais sans former de logettes
latérales ; il existe donc comme dans ce dernier genre une couche équato-
riale de logettes, mais elles sont rectangulaires comme dans Heterostegina.
Les couches latérales sont compactes et plus épaisses au centre, ce qui
donne aux échantillons une forme lenticulaire ordinairement trés aplatie.
L’ornementation dans Cycl. communis est formée par une série de
granules disposés suivant les anneaux d’accroissement, et correspondant
a des piliers analogues a ceux des Orbitoides.
Cette espéce est trés abondante dans les couches supérieures de Vile
de Batan (éch. n° 8) ow elle accompagne les Myogipsina et dans les cal-
caires tendres jaundtres du Barrio de Mesaba (Cebu, n° 273), ot elle
est associée 4 Operculina costata. J’ai déja montré précédemment que
le premier niveau appartenait au Burdigalien, tandis que le second parait
devoir se placer au sommet de l’Aquitanien. Cette espéce dans les Phil-
ippines se montrerait ainsi a la base de H et dans G, 4 peu prés au
méme niveau qu’a Bornéo; il est méme possible que les calcaires tendres
jaunatres du Barrio de Mesaba représentent exactement les couches a silex
du groupe F de Bornéo.*
ROTALIA.
J’ai pu extraire de la roche tendre de Old Alpaco Mines (éch. n° 273)
de petits échantillons qui ressemblent beaucoup a Rotalia schroteriana
Parker et Jones, avec ses lignes d’enfoncements le long des cloisons,
mais qui en différent par une forme moins dissymétrique. I] semble
que Carpenter a eu sous les yeux une forme bien voisine quand il dit:°
“dans une remarquable variété des iles Fidji la spire est plus symétrique
5 Spore de sorte que la coquille a presque la méme forme que Polys-
* Bull. Soc. géol. France (1905), IV, 5, 445. * Introduction, 213.
58 DOUVILLE.
tomella craticulata; elle se rapproche du reste beaucoup de ce type
par la disposition du dépét exogéne et par la maniere dont les passages
interseptaux s’ouvrent extérieurement le long du bord des cloisons.”
A la page suivante il revient sur ces analogies avec Polystomella, qui
montrent que ces deux types sont extrémement voisins l’un de l’autre.
Tl est curieux de retrouver aux Philippines ces deux formes associées dans
le méme gisement.
POLYSTOMELLA.
Forme voisine de P. craticulata, mais a callosité ombilicale un peu
moins large et moins développée; on sait que ce genre est abondant a
partir du Tertiaire moyen. Cette forme est associée a la précédente
dans le grés tendre de la vieille mine d’Alpaco (éch. n° 273).
Une forme trés yoisine est indiquée par des sections dans les caleaires
oligocénes 4 petites Nummulites de Caracaran de Vile de Batan (éch.
n° 2). Une coupe axiale passant par le centre montre que c’est bien
un Polystomella et non un Rotaha. Ce type aurait done apparu dés
la fin de l’Oligocene.
Nummulites subniasi sp. nov.
Nummulina variolaria Brady, On Some Fossil Foraminifera from the West
Coast District of Sumatra. Geol. Mag. (1875), Il, 2, 552.
Les calcaires subordonnés aux couches de charbon de Vile de Batan
renferment de nombreuses petites Nummulites qu’il ne semble pas
possible de distinguer de celles que M. Verbeek a recueillies autrefois
dans Vile de Nias et qui ont été décrites et figurées par Brady sous
le nom de NV. variolaria; cet auteur donne comme dimension maxmium
2 millimetres et ses figures indiquent bien des individus mégaspheriques.
Les échantillons des Philippines sont légérement plus grands, 2.7 milli-
metres, et sont également mégasphériques comme l’indique la coupe ci-
jointe.
La forme de la spire, la direction et la courbure des cloisons concordent
parfaitement. —
En 1896, M. Verbeek a repris l’étude de cette espéce et a figuré a
“nouveau sous le nom de Nummulites niasi II, une forme un peu plus
grande, ayant un diamétre de 4 millimétres mais
certainement microsphérique comme le montre le
diamétre de la loge initiale pour lequel M. Verbeek
donne la dimension de 0.02 millimétre. Comme le
Nummulites niasi 1 Verbeek est incontestablement
une Amphistégine, on pourra réserver a la NV. aast
Fic. 1—Nummulites II microsphérique le nom spécifique de niasi Ver-
la Ce age beek, et donner a notre forme mégasphérique le nom
bonneuse de l’ile de d Brains’
Batan, gr. 10 fois. e swoniast.
LES FORAMINIFERES. 59
LEPIDOCYCLINA.
Dans un mémoire précédent et & exemple de MM. Verbeek et Fen-
nema, j’ai divisé ce genre en deux sections, pour lesquelles j’ai proposé
les noms suivants:
1° Les Hulepidina généralement de grande taille, caractérisées par
leurs loges équatoriales en spatule ou en hexagone subrégulier et par
leur nucleus du type embrassant.
2° Les Nephrolepidina, presque toujours petites, 4 loges équatoriales
ogivales, en losange ou en hexagone allongé et 4 nucleus du type réni-
forme.
Je vais examiner séparément chacun de ces groupes.
1° Section des Eulepidina.
Dans les Philippines ces grandes formes paraissent cantonnées dans
les Caleaires 4 Orbitoides inférieurs et dans les marnes subordonnées;
le Tertiaire de cet archipel présente de telles analogies avec celui des
Archipels voisins, qwil n’est pas possible de séparer V’étude de leurs
fossiles. Je passerai done tout d’abord rapidement en revue les espéces
qui ont été proposées dans cette région. Elles sont malheureusement le
plus souvent trés incomplétement définies et il ne sera pas toujours
possible de les caractériser d’une maniére certaine.
L’étude approfondie que j’ai pu faire des différentes espéces de Lepi-
docyclina mn’a montré que les caractéres les plus précis sont fournis par
la disposition des piliers et des logettes laterales; ces caractéres ne sont
que tres rarement indiqués, les espéces
étant principalement établies sur de sim-
ples sections.
C’est Brady qui en 18757 a décrit et
figuré les premiéres espéeces d’apres des
échantillons recueillis par M. Verbeek et
envoyés par ce géologue a Rupert Jones; Be 2 sing He oe ABAD
ils provenaient en particulier de l’ile de 9 Brady:
Nias. La plupart des formes ont été attribuées a tort a des espéces déja
connues, Nummulina variolaria, N. ramondi, Orbitoides papyracea, O.
dispansa; une seule espéce nouvelle est proposée:
(1) Orbitoides sumatrensis, trés bien figurée
(loc. cit. Pl. XIV, fig. 3, ab.) ; c’est une forme
globuleuse, presque sphérique, ayant environ 3
millimétres de diamétre, sur une épaisseur de
2.5 environ. Elle présente a ’équateur une mince Fie. 2>!s—Section d'un
x , : , échantillon de l'ile de
eollerette trés étroite, dont le contour présente Nias, gr. 10 fois.
*Geol. Mag. (1875), 2, 532. On Some Fossils Foraminifera from the West
Coast District of Sumatra.
60 DOUVILLE.
des parties saillantes dessinant une sorte d’étoile; la premiére loge parait
trés petite. :
Blle a été recueillie dans Vile de Nias. M. le D™ Verbeek a bien voulu
me communiquer plusieurs échantillons provenant de la localité type.
J’ai pu m/’assurer ainsi qu’elle appartenait a la section des Nephrolepi-
dina. Hlle différe trés notablement des formes de l’Aquitaine qui en
ont été rapprochées.
Quelques-années aprés, en 1880, le professeur K. Martin ® a fait con-
naitre de nouvelles espéces qu’il range avec
raison dans les Lepidocyclina.
(2) Orbitoides carteri (loc. cit., p. 11, Pl.
XIV, fig. 2, 2a, 2b, 2c) ; elle est lenticulaire
et légerement renflée au centre, elle atteint
Fic. 3.—lLepidocyclina car- un diamétre de 26 millimétres avec une
teri. Martin, disposition » ; Riera
des piliers prés de la sur. ¢Paisseur maximum de 2 millimétres. La
Teco met pz0 ols. surface ne montre d’aprés l’auteur aucune
ornementation ; toutefois la fig. 2a montre des piliers inégaux, penta-
gonaux, quadrangulaires, ou triangulaires dont l’épaisseur est indiquée
comme étant de 0.05 a 0.12 millimétre. Sur une des préparations qui
m’a été communiquée par le professeur R. Martin, on distingue des piliers
peu développés se présentant comme des épaississements des points de
rencontre des cloisons, peu nombreux et irréguliérement distribués; ils
sont triangulaires, quadrangulaires et trés exceptionnellement pentago-
naux. Mais la préparation est trés voisine de la couche équatoriale et il
est possible que les piliers se développent davantage dans les couches plus
extérieures et dans la partie centrale qui est un peu renflée; et en effect,
les coupes axiales montrent de gros piliers qui sont probablement des
pustules et qui atteignent la dimension indiquée de 12 millimétres. Les
logettes latérales ont de 0.08 a 0.11 millimétre de diamétre et leurs parois
0.03 a 0.035 d’épaisseur. Elles forment des couches trés nombreuses, 30
environ ati centre. la figure 26 montre les perforations du toit de cer-
taines logettes sous la forme de fins canaux paralléles.
La gangue est un tuf grossier renfermant des fragments de roche
éruptive et de nombreux Cycloclypeus communis.
La localité originaire est au Nord de Sindangabaran? (Java). D’apreés
la forme des logettes équatoriales cette espéce appartient bien certaine-
ment a la section des Eulepidina.
(3) Orbitoides gigantea (loc. cit., p. 20, Pl. XIV, fig. 3, 3a, 3b, 3¢,
3d) différe de la précédente par sa taille plus grande, presque double,
50 millimétres; la forme générale est la méme. Une section tangentielle
8 Untersuchungen iiber die Organisation von Cycloclypeus und Orbitoides.
Niederl. Arch. f. Zoél. (1880), 5.
LES FORAMINIFERES. 61
communiquée par le professeur K. Martin, montre une série de piliers
assez gros atteignant 0.15 millimétre et entourés de 6 4 7 logettes; ils
constituent done de véritables pustules, assez souvent
séparées par deux ranqées de logettes; celles-ci sont
de forme assez irréguliére et leur plus grande dimen-
sion varie de 0.1 4 0.2 millimétre.
D’aprés Vauteur cette espéce se distingue aussi de
la precedente par ses logettes latérales plus hautes et
formant des couches moins nombreuses.
L’espece est fondée sur un seul échantillon incom-
plet provenant de Tjidamar (Java).
(4) Orbitoides radiata (loc. cit., p. 22, Pl. XIV,
fig. 4) presente sur sa surface un bouton central d’?ot Fie. 4—Zepidocy-
4 O 5 . cling gigantea
partent 9 rayons saillants qui n’atteignent pas le Martin. Atecdsltion
y H Eee : A ay SUE ? des piliers prés de
bord. Elle provient de la méme localité que 0. la surface, gr. 20
cartert. L’auteur ’a Vabord rangéé dans les Acti- — *4s.
nocyclina, mais il a reconnu plus tard® que c’était une véritable Lepi-
docyclina.
Le méme auteur avait décrit *° en 1891 une cinquiéme espéce:
(5) Lepidocyclina multipartita, petite forme de 6 4 7 millimétres de
diameétre, trés renflée au milieu et présentant quelques grosses pustules ;
la couche équatoriale se renfle beaucoup 4 la périphérie et elle se subdivise
alors dans la hauteur d’une maniére irréguliére. Elle appartient vrai-
semblablement 4 la section des Nephrolepidina. Elle provient des cou-
ches a Cycl. annulatus.
En 1896, MM. Verbeek et Fennema* publiaient leur grand ouvrage
sur Vile de Java et donnaient d’excellentes figures d’un grand nombre
de Foraminiféres, Alveolina, Nummulites, Operculina, Orbitoides, ete.
Ils indiquent pour la premiére fois que les Orbitoides a loges équatoriales
rectangulaires (distinguées en 1868 par Gumbel sous les noms de Dis-
cocyclina, Rhipidocyclina, Aktinocyclina, et Asterocyclina, réunies plus
tard en 1891 par Munier-Chalmas sous celui d’Orthophragmina), se
recontrent exclusivement dans le tertiaire ancien ayec les Nwmmulites,
tandis que les Lepidocyclina caractérisent le Miocene.
Ces auteurs distinguent dans ce dernier genre 6 espéces réparties en
3 couples, mais sans leur donner de noms: le premier avec des logettes
équatoriales en losange appartient a la section des Nephrolepidina,; il
comprend les formes microsphériques I A (a, d, h, 1) et mégasphériques
IB, (9, i). les deux autres ont des logettes équatoriales en spatule et
font partie de la section pour laquelle j’ai proposé le nom de Hulepidina;
°In Schlumberger, 1900.
1 Samml. Geol. Mus. Leiden (1881), Neue Folge, 1, Heft I, 7, Pl. 1. fig. 7-10.
" Description géologique de Java et Madura.
62 DOUVILLE.
elles sont petites, 5 a 6 millimétres, Il C (f) et IL D (e), ou grandes,
atteignant jusqu’a 70 millimetres, III E (b, m, n) et Ill F (¢, ¢, p).
Ils considérent les O. carteri et O. gigantea comme se rapportant proba-
blement a l’espéce III E, et ils ajoutent que “certaimes espéces se recon-
trant dans 2 ou méme 3 étages, il ne semble pas qu’elles puissent convenir
pour établir des subdivisions dans les couches néogenes.”
En 1899, Newton et Holland,’* reprennent l’étude des principales
formes décrites par Brady: cest ainsi qwils donnent le nom de (6)
Lepidocyclina verbeecki a VOrb. papyracea de Brady a laquelle ils réunis-
sent les formes g et k de Verbeek et Fennema. Or, ces différentes formes
sont mégasphériques et ’O. papyracea, de méme que la forme k, provien-
nent de Padang; le nom de Lep. verbeeki doit done strictement étre
réservé pour les formes mégasphériques de Padang. J’en ai sous les
yeux un grand nombre d’échantillons communiquées par M. Verbeek et
provenant de la localité type; ils ont de 5 a 7 millimétres de diamétre ;
ils sont amincis sur les bords et assez fortement renflés au centre; quand
la surface est bien conseryée elle est lisse mais on y distingue néanmoins
une vingtaine de petites pustules subégales ayant de 0.15 a 0.2 milli-
métre; cette disposition est assez bien indiquée sur une coupe tangen-
tielle figurée par Newton et Holland (loc. cit., Pl. IX, fig. 10) dans
laquelle cependant les pustules sont plus petites et paraissent indiquer
un individu jeune. ‘
Vers 1900, Rupert Jones et Chapman ont décrit et figuré ** un grand
nombre d’Orbitoides provenant de Vile Christmas; malheureusement les
échantillons n’ont pas été isolés et les espéces ne sont établies que sur
des sections effectuées dans la roche qui les contient et, par suite, d’une
orientation incertaine: aussi la plupart d’entre elles doivent étre con-
sidérées comme insuffisamment définies.
Ainsi (7) L. meodispansa, rapprochée de la forme d de Verbeek et
Fennema est une Nephrolepidina de 5 millimétres de diamétre qui re-
semble beaucoup a Lep. verbeeki; cependant les pustules paraissent plus
grosses et moins nombreuses. Le caractére distinctif, mdiqué par les
auteurs et fondé sur le renflement plus brusque de la partie centrale,
nest guére applicable. En outre, il ne semble pas d’aprés les sections
figurées que Vespéce soit microsphérique comme d de Verbeek et Fen-
nema.
(8) L. insule-natalis est exceptionellement susceptible d’une defini-
tion plus précise. Sa grande taille, 12.5 a 19 millimétres, la range
“On some tertiary Foraminifera from Borneo and their comparison with
similar forms from Sumatra. Ann. & Mag. Nat. Hist. (1901), VII, 7, 215.
** On the Foraminifera of the Orbitoidal limestones and reef rocks of Christmas
island. Ce mémoire fait partie d’une monographie de ces iles; le tirage 4 part
ne porte ni titre général, ni date, ni indication d’éditeur. On sait que Jile
Christmas est située A environ 3 degrés 1/2 de latitude au Sud de la pointe
occidentale de Java.
LES FORAMINIFERES. 63
dans les Hulepidina; la figure type (loc. cit., Pl. XX, fig. 5) est une
section oblique et ne passant pas par le centre, comme le montre l’inéga-
lité des deux moitiés. Il en résulte que la moitié la plus grande re-
présente une coupe en partie perpendiculaire au rayon, e’est 4 dire
tangentielle. Elle montre bien la disposition des piliers, qui, comme
Vindique expressément Vauteur, “entourent les logettes polygonales.”
Cette disposition est bien indiquée sur la figure ci-jointe qui représente
un grossissement de la figure type; elle est tout
a fait caractéristique du groupe du Lepidocy-
clina dilatata.
C’est done a tort que Schlumberger a at- &
tribué a cette espéce un échantillon de Java |
dont la surface présente de nombreuses pustules
entourées par les logettes. Cette disposition est
inverse de la précédente et il faudra conserver aap teh ao laepantie cata
pour Vespéce de ce dernier auteur le nom qu’il © 412, fgure type de MM.
; : ? : Rupert Jones et Chapman,
avait tout d’abord choisi L. ngembakt. HO ROSATO GO) alae
(9) L. ephippioides est rapproché a la fois aiqué oa tal has
de Vespéce précédente qui est un Hulepidina
et de L. verbeeki qui est un Nephrolepidina; c’est dire combien elle est
yaguement définie. L’épaisseur des cloisons pourrait faire penser 4 une
forme du groupe de L. formosa Schlumb.
(10) ZL. murrayana a 4 rayons n’est probablement pas une forme
étoilée comme Vont pensé les auteurs, mais simplement une forme en
selle; les caractéres donnés sont dés lors tout a fait insuffisants.
(11) L. andrewsiana; le seul caractére indiqué est le fort renflement
central avec large collerette, il est également insuffisant.
En 1900, Schlumberger ** décrit deux nouvelles espéces de Lépidocy-
clines :
(12) L. ngembaki, qu'il attribue 4 tort 4 L. imsule-natalis J. et Ch.
comme je viens de le montrer. Dans cette derniere espéce les piliers
restent polygonaux, se rejoignent en grossissant et entourent les logettes,
tandis que dans la nouvelle espéce les piliers restent isolés et se trans-
forment en pustules entourées chacune par une rosette de logettes.
Cette disposition est trés nettement indiquée par l’auteur (loc. cit.,
Pl. VI, fig. 4) sur une coupe tangentielle grossie 20 fois. Il faut done
reprendre le nom que l’auteur avait adopté tout d’abord, avant d’avoir
recu le mémoire de Rup. Jones et Chapman (loe. cit., p. 130).
Les piliers sont trés petits et ne dépassent pas 0.1 millimétre, tandis
que les logettes qui les séparent ont au centre seulement 0.06 de largeur.
L’échantillon type avait été recueilli a Ngembak (Java) par M. Ver-
beek.
“Notice sur deux espéces de Lépidocyclines des Indes néerlandaises. Samm.
d. geol. r. Museums in Leiden (1900) I, 6, fase. 3, 128.
64 DOUVILLE.
(13) L. martini (loe. cit., p. 131, Pl. VI, fig. 5 et 8) est une forme
étoilee de Batoe Koetjing (residence de Madoera) qui a été rencontrée
dans les Caleaires a Cycloclypeus. :
Le méme auteur publiait un peu plus tard 1° en 1902 une troisiéme
espéce de Lépidocycline: (14) ZL. formosa qui mérite de nous arréter
un instant. Hlle n’est connue que par des coupes; or l’une Welles (loc
cit., Pl. VII, fig. 2) montre une partie centrale quadrangulaire pro-
longée aux 4 sommets par des branches étroites. L’auteur a pensé qwil
sagissait dune forme rayonnée: en réalité c’est simplement une forme
discoide recourbée en selle: on sait que dans ce cas la couche équatoriale
se rapproche d’un hyperboloide dont les sections dans le voisinage du
plan tangent au centre sont constituées par deux hyperboles; de 1a les
4 branches de la figure précitée.
Au centre cette coupe montre un nucleus du type embrassant. Grace
a Vobligeance de M. le Professeur Haug j’ai pu retrouver dans la collec-
tion Schlumberger, conservée 4 la Sorbonne, une
moitié de Véchantillon dont il vient d’étre ques-
tion; une préparation tangentielle a montré la
disposition des logettes latérales séparées par des
cloisons épaisses et paraissant dépourvues de
Fie. 6.—Lepidocyclina piliers. Sur un autre échantillon de la méme
formosa, disposition : ten aie
des logettes sur une P!OVenance, les logettes atteignent 0.2 millimétre
fon tepe de lessees, de diamétre et les cloisons qui les séparent ont
i 2D Hors: en moyenne 0.1 millimetre d’épaisseur.
L’échantillon lui-méme présente une partie centrale globuleuse at-
teignant 6 millimétre de diamétre avec une épaisseur de 4.2 milli-
metres (et non de 2 millimétres comme l’auteur l’indique par erreur) ;
tout autour s’étend une collerette mince de 6 millimetres environ de
largeur et de moins de 1 millimétre d’épaisseur.
Cette espéce provient de Teweh (Bornéo).
Newton et Holland avaient déja publié en 1900 7° quelques notes sur
des Foraminiféres de Formose; ils reviennent sur le méme sujet en
1902 ** et signalent dans ces calcaires une série de petites Lépidocyclines
L. sumatrensis, L. verbeeki et une espéce nouvelle (15) L. angularis
présentant un renflement central orné de grosses pustules et légérement
déprimé au centre, ce que indique l’existence d’une couronne de pustules
plus développées que les pustules du centre; c’est une disposition qui
Q
rappelle celle de certaines L. morgan. Le diamétre est de 3 millimetres
* Sur un Lepidoeyelina nouveau de Bornéo. Ibid. (1902), 6, 251.
**Notes on Microscopie Sections of Limestones from Formosa, Collected by
Dt Koto of Japan. Journ. Geol. Soc. Tokyo (1900), 7, 1-4.
* On Some Fossils from the Islands of Formosa and Riu-Kiu (=Loo Choo).
Journ. Coll. Sc. Imp. Univ. Tokyo (1902), 17, article 6.
LES FORAMINIFERES. 65
ayec 1 millimétre d’épaisseur; les auteurs indiquent la coexistence de
formes micro-et mégasphériques.
Dans leur mémoire sur le genre Lepidocyclina, MM. Paul Lemoine
et Robert Douvillé 1 ont décrit quelques formes provenant de Madagascar
et de lAfrique orientale allemande; ces gisements se rattachent étroite-
ment 4 ceux des iles de la Sonde et font certainement partie du méme
bassin. Je laisse de cété parmi les espéces citées, LZ. mantelli, dont
Vattribution principalement fondée sur des coupes axiales semble bien
douteuse; L. raulint insuffisamment caractérisée et L. morgani; deux
espéces nouvelles doivent étre examinées de plus prés: (16) Lepidocy-
clina joffret est représentée par une coupe équatoriale et une coupe axiale
et caractérisée surtout par la grandeur du nucleus qui atteint 2 milli-
métres ; elle est considerée par les auteurs comme une simple race de la
L. dilatata,; les cavactéres des logettes latérales et des piliers ne sont pas
indiqués; d’aprés les auteurs la surface serait lisse. Cette espéce aurait
besoin d’étre étudiée 4 nouveau.
La deuxiéme forme (17) ZL. gallieni ressemble beaucoup a L. dila-
tata, mais, disent les auteurs, les coupes montrent’ des loges environ deux
fois plus petites linéairement, et séparées par de petits piliers fins (ce
qui est parfaitement exact) mais un peu plus gros que ceux de L. dila-
tata (ce qui n’est vrai que pour les piliers que l’on observe sur les bords
dans cette derniére espéce, ceux du milieu étant au contraire beaucoup
plus gros.) Néanmoins les auteurs ont parfaitement saisi le caractére
principal de cette espéce, caractére du reste commun avec presque toutes
les formes de l’Extréme Orient d’avoir les logettes
bien plus petites que les espéces de la région médi-
terranéenne.
Jai sous les yeux le type de V’espéce: la surface
extérieure polie montre des logettes trés arrondies
qallienti de Mada- ayant en moyenne 0.1 millimetre de diametre sépa-
gasecar; coupe prés
de la surface mon-
aa piliers me 99 Piliers aux points de croisement de ces cloisons,
HOS: quadrangulaires, pentagonaux ou hexagonaux ayant
a peu pres la méme largeur que les cloisons. Ces piliers couvrent a peu
pres toute la surface de la coquille 4 ’exception de la zone marginale.
On voit que cette forme est trés voisine de (2) L. carteri; les dimen-
sions des logettes sont analogues, mais dans cette derniére espéce les
piliers paraissent moins développés.
Plus récemment M. Warren D. Smith a publié une série de travaux
trés importants sur la géologie des Philippines: il a décrit et figuré
plusiers espéces de Lépidocyclines.
rées par des cloisons épaisses avec de nombreux
#8 Uém. Soc. géol. de France, Paléontologie, (1904), 12, n° 32.
66 DOUVILLE.
En 1906 il a étudé les Orbitoides de Binangonan.® Cette localité
avait été signalée par Richthofen,*® qui disait y avoir recueilli une
grande quantité de Nummulites de diverses grosseurs et appartenant a
plusieurs espéces. M. Warren D. Smith n’y a trouvé que des Lépido-
eyclines: il déerit et figure sous le nom de (18) Orbitoides richthofeni
(loc. cit., Pl. I, fig. 1) une espéce de grande taille qui devait attemdre
36 millimétres de diamétre avec une épaisseur maxima de 8 millime-
tres. L’auteur a bien youlu me communiquer la preparation figurée:
e’est une section oblique et ne passant pas par le centre, comme le montre
Vinégalité des deux moitiés, de part et d’autre du plan équatorial. Au
milieu du cdté le plus large on distingue un élément de coupe tangen-
tielle (c’est a dire perpendiculaire au rayon) dans laquelle on voit que
les logettes sont séparées par des cloisons trés épaisses; c’est un carac-
tére que Von ne retrouve que dans le groupe de la Lep. formosa. D’un
autre cété Véchantillon est partiellement dissous dans la region péri-
phérique, les piliers plus résistants devraient ¢tre conservés; or il font
défaut, ce qui indique quil n’en existait probablement pas. On peut
chercher 4 se rendre compte de l’épaisseur des cloisons par leur largeur
minima dans la coupe, elle est environ la moitié de celle des logettes.
Ces caractéres Indiquent bien une espéce du groupe de L. formosa, mais
la forme générale parait assez différente, ’échantillon étant beaucoup
moins globuleux. I] serait done nécessaire d’examiner d’autres échan-
tillons pour préciser les caractéres de l’espéce.
La figure 2 de la méme planche reproduit la section d’un autre échan-
tillon bien plus voisin par sa forme et Vensemble de ses caractéres de
L. formosa.
Peu aprés le méme auteur ** publiait la description d’une série de
fossiles provenant également de Vile de Luzon, mais au Sud de Manille.
Dans cette région le Miocene a Vicarya callosa repose directement sur
des roches éruptives; il signale dans ces couches et décrit sous le nom
de (19) Orbitoides martim une Lépidocycline (loc. cit., p. 628, Pl. IV,
fig. 6, 7, 8) de forme lenticulaire dont le diamétre varie de 15 4 50 milli-
metres. J’ai entre les mains la coupe axiale (fig. 8), elle ne montre
pas de piliers nets, mais seulement des parois de loges un peu épaissies.
L’auteur dit que des formes analogues sont abondantes dans les cal-
caires de Cebit; je serai en effect porté a en rapprocher les échantillons
de la vallée de Cumajumayan (éch. n° 285). Mais comme le nom de
L. martina a déja été employé en 1900 par Schlumberger, il ne peut
étre conserve.
” This Journal (1906), 1, 203.
* Ueber das workommen von Nummulitenformation auf Japan und den Phil-
ippinen. Ztsch. deutch. Geol. Ges., (1862), 14, 357.
* Preliminary Geological Reconnaissance of the Loboo mountains of Batangas
Province. Jbid (1906), 1, 617.
LES FORAMINIFERES. 67
Tout récemment des travaux importants ont été publiés en Italie sur
des Foraminiféres recueillis par le D™ Bonarelli dans les iles de la Sonde.
C’est d’abord un mémoire de M®*® Giuseppina Osimo * sur des Fora-
miniféres de Dongola, sur la cdte occidentale de Celebes, 4 Ventrée de
la baie de Palos. Parmi les formes figurées et décrites par Vauteur je
signalerai une série de petites ou tres petites Nummulites a filets rayon-
nants parmi lesquelles NV. elegans, Vaprés laquelle Vauteur attribue ce
niveau au Bartonien; Amphistegina niasi et deux Lépidocyclines: L.
tournowen et une forme nouvelle (20) Lepidocyclina provalei, repré-
sentée par un seul exemplaire de 7 a 8 millimétres de diamétre et une
épaisseur d’environ 5 millimetres. Toute la surface est couverte de
granulations saillantes de grosseur croissante de la périphérie vers le
centre, ot elles atteignent 0.2 millimetre; elles sont séparées d’apres
Vauteur par une seule rangée de logettes. Cette disposition rappelle
tout 4 fait celle de L. ngembaki, mais ici les piliers sont moins uniformes
et atteignent au centre une grosseur presque double.
Immédiatement aprés, le méme recueil a publié deux mémoires de
M'e Irvéne Provale** sur des Foraminiféres de Bornéo recueillis égale-
ment par le D™ Bonarelli. Ils proviennent de différentes localités, et
Vauteur distingue plusiers niveaux différents: un niveau inférieur a
petites Nummulites et a Orthophragmina attribué a l’Wocéne supérieur,
un niveau moyen a Lépidocyclina schlumbergeri, raulini, tournoueri et
a Nummulites fichteli représentant !’Oligocéne et un niveau supérieur
miocéne a petites Lépidocyclines. I] est peu probable que les Lépido-
eyclines du niveau moyen soient identiques aux especes de France dont
Vauteur les rapproche; en particulier les figures données de L. raulini
indiquent une forme a logettes bien plus petites, mais les descriptions
sont insuffisantes pour déterminer leurs affinités réelles.
Dans la deuxiéme partie V’auteur figure une Lep. formosa certaine-
ment analogue au type, mais en différant par sa forme bien moins globu-
leuse, et une L. insule-natalis, espéce 4 laquelle il rapporte le L. ngem-
baki de Schlumberger et L. provalei de M"* Osimo.
Ces deux derniéres especes sont en effet trés voisines comme je viens
de Vindiquer, mais elles sont trés différentes du L. insule-natalis (8)
comme je l’ai fait voir précédemment. Du reste l’échantillon figuré sous
ce nom (PI. III, fig. 4, 5, 6) est extrémement globuleux et rappellerait
plutét L. swmatrensis.
Une curieuse espéce nouvelle est (21) L. ferreroi qui avait été recuei-
llie il y a déja longtemps 4 Sumatra par M. Verbeek et & Madagascar
#Di aleuni Foraminiferi dell’eocene superiore di Celebes. Rivista italiana
di Paleontologia, Anno XIV (1908), 28-54, Pl. I-III.
Di aleune Nummulitine e Orbitoidina dell’ isola di Borneo, deux parties.
Rivista italiana di Paleontologia, Anno XIV (1908), 55-80, Pl. IV-VI et Anno
XV (1909), 65, Pl. II, III.
68 - DOUVILLE.
par M. Lemoine. Hlle est caractérisée par 3, 4 ou 5 grosses pustules
saillantes placées a une certaine distance du centre.
Il faut signaler encore plusieurs variétiés de Lep. towrnowert a rap-
porter probablement a Lep. verbeeki:
1. Var. angulosa (22) (loc. cit., Pl. Il, fig. 18, 14, 15), caractérisee
par 5 grosses pustules disposées en couronne autour du centre: parait
voisine de L. angularis (15) de Newton et Holland.
2. Var. mflata (23) (loc. cit., Pl. III, fig. 14, 15) avec wne grosse
pustule au centre. ;
3. Var. borneénsis (24) (loc. cit., fig. 16-19) avec les granules unifor-
mément répartis sur la surface et un nucleus souvent irrégulier et pluri-
loculaire.
Résumé.—Il resulte de cette longue révision qu’un assez grand nombre
W@espéces de Lépidocyclines provenant des Indes Orientales** ont deja
été décrites par les différents auteurs; certaines formes ont été rappro-
chées des espéces d’Hurope, tandis que d’autres ont été considérées comme
spéciales. Une étude attentive montre presque toujours que les espéces
indiennes sont différentes des formes européennes ; en particulier le réseau
est ordinairement 4 mailles notablement plus petites; ce caractére signalé
par MM. Lemoine et R. Douvillé pour des formes de Madagascar parait
se retrouver dans toutes les espéces des Indes orientales. Il semble done
préférable d’étre trés réservé dams ces assimilations. Mais si ces deux
groupes de formes sont différents, elles forment en réalité deux séries
paralléles et constituées par des espéces correspondantes, c’est a dire pré-
sentant le méme degré d’évolution.
J’ai précédemment groupé les espéces de Lépidocyclines en deux sec-
tions: Hulepidina et Nephrolepidina fondées sur la forme des loges
équatoriales (en spatule ou en ogiye) et sur la disposition du nucleus
(deuxiéme loge embrassante ou réniforme) ; je vais examiner successive-
ment les espéces qui ont été distinguées dans chacun de ces groupes.
Dans les Hulepidina les caractéres les plus précis sont donnés par la
disposition des piliers; il est facile de se rendre compte que ces derniers
prennent naissance aux points de rencontre des cloisons des logettes
équatoriales; les premiéres couches des logettes latérales correspondent
aux logettes équatoriales et sont par suite 4 peu prés hexagonales; on
distinguerait alors sur leur pourtour 6 ébauches de piliers; chacun d’eux
ayant une section triangulaire. Mais les piliers se développent mégale-
ment tandis que les logettes se déforment plus ou moins rapidement.
Dans les formes les moins évoluées les piliers restent polygonaux a 3.4
ou 5 cétés; ils forment une ceinture discontinue autour de chaque logette,
*t Je comprends sous cette denomination l’ensemble des iles en bordure du
continent depuis Madagascar jusqu’au Japon et les portions du rivage qui s’y
rattachent au point de vue géologique.
LES FORAMINIFERES. 69
cest le stade n° 1. Presque toujours les piliers se développent davantage
dans la partie médiane ordinairement renflée, mamillée, ils se rejoignent
alors assez souvent et entourent plus ou moins complétement les logettes,
cest le stade n° 2.
Dans un troisiéme cas les piliers qui se développent sont moins nom-
breux et restent isolés tout en étant encore polygonaux A 3.4 ou 5 cétés
(stade n° 3).
Enfin ils peuvent prendre une importance plus grande et autour de
chacun d’eux on distingue une sorte de rosette formée de nombreuses
logettes; on dit alors que les piliers sont devenus des pustules (stade
n° 4). Cette disposition peut se développer seulement dans le mamelon
central ou envahir une partie plus ou moins grande de la surface de la
coquille.
D’une maniére générale une méme section tangentielle oblique pourra
montrer en se dirigeant de la couche équatoriale vers le centre les diffé-
rents stades de développement des piliers, et c’est d’ordinaire au centre
que ceux-ci seront le plus spécialisés.
Une disposition toute différente se rencontre dans certaines espéces
ou toutes les cloisons s’épaississent sans former de piliers proprement
dits (stade n° 5).
Exceptionnellement les piliers peuvent ne pas se développer et man-
quer completement. Nous distinguerons cette disposition comme stade
mou:
D’aprés ces considérations on peut distinguer parmi les espéces déja
connues :
1° Lepidocyclina carteri Martin (2.1880) caractérisé par le stade n° 1,
nombreux petits piliers a 3, 4, ou 5 cétés. La coquille est mince, 4 peine
renflée au centre ot les piliers ne présentent pas de développement spé-
cial. On sait que les couches latérales sont minces et trés nombreuses.
2° Lepidocyclina gallienti Lemoine et R. Douyillé (17.1904) présente
comme l’espéce précédente de trés nombreux piliers 4 3.4 ou 5 cétés. Ls
sont un peu plus développés, les cloisons sont plus épaisses et les logettes
latérales plus arrondies ; mais ces différences ne sont guére que des diffé-
rences de races. Hn outre il n’était pas possible de s’en rendre compte
au moment ou l’espéce de Madagascar a été établie, le L. cartert étant
trés incomplétement défini.
3° Lepidocyclina insule-natalis J. et Ch. (8.1900) ; les piliers sont
plus développés et viennent se rejoindre partiellement en formant autour
des logettes une ceinture plus ou moins discontinue (stade n° 2) ; c’est
au centre qwils atteignent leur développement maximum.
Les trois espéces qui précédent et en particulier la derniére corres-
pondent par la forme et le développement de leurs piliers a L. dilatata,
‘ 101776——2
70 DOUVILLE.
Mich. d’Europe; elles n’en différent guére que par la plus grande finesse
du réseau.
4° Lepidocyclina gigantea Martin (3.1880); les piliers sont moins
nombreux, isolés les uns des autres et forment presque des pustules,
séparés souvent par plusieurs rangées de logettes (stade n° 3); Cest
une disposition qui rappelle celle de L. elephantina Mun. Chalm.
5° Lepidocyclina provalei Osimo (20.1908) ; les pustules sont ici net-
tement caractérisées et elles sont séparées par une seule rangée de loget-
tes; leur grosseur augmente progressivement quand on se rapproche du
milieu de la coquille.
6° Lepidocyclina ngembaki Schlumberger (12.1900) présente également
des pustules bien caractérisées quoique tres petites; elles sont séparées
au moins au centre par une seule rangée de logettes, et elles sont de
grosseur uniforme, ce qui distingue cette espéce de la précédente.
7° Lepidocyclina formosa Schlumberger (14.1902) se distingue de
toutes les formes précédentes par l’épaisseur de ses cloisons, et absence
de véritables piliers.
Dans les Nephrolepidina les pustules existent presque toujours, mais
leur disposition fournit de bons caractéres.
8° Lepidocyclina verbeeki N. et H. (6.1899), est la forme fondamen-
tale correspondant a L. towrnoueri Lem. et R. D., d@Hurope. Cvest
comme cette derniére une forme mégasphérique et elle s’en distingue par
son réseau beaucoup plus fin; il suffit pour s’en rendre compte de com-
parer les figures 8 de Newton et Holland ?° et 1 de Lemoine et Rob.
Douyillé,?® qui représentent les coupes équatoriales de ces deux espéces
a un grossissement analogue, 20 et 18 fois.
Cette espéce présente de nombreuses pustules dont la grosseur ya en _
croissant de la périphérie au centre.
On pourrait distinguer par des noms spéciaux les formes suiyantes:
9° Lepidocyclina inflata Provale (23.1909) caractérisée par une tres
grosse pustule médiane. :
10° Lepidocychina angularis Newton et Holland (15.1902) présente
une couronne de grosses pustules plus développées que les pustules
médianes. Hlle correspond a peu prés au Lep. morgam d Hurope.
11° Enfin une forme trés particuliére est Lep. ferreroi Provale (21.
1908) dont la surface présente seulement 3 4 5 gros boutons saillants
disposés en étoile autour du centre qui est déprimé.
Nous pouvons maintenant aborder l’examen des échantillons des Phil-
ippines, il sera facile de distinguer les formes suivantes:
= Ann. & Mag. Nat. Hist. (1899), VII, 3, pl. 9.
7° Mem. Soc. géol. Fr., Paléontologie (1904), 12, Pl. III.
LES FORAMINIFERES. 71
A. Section des Eulepidina.
1° Formes grandes, minces ou lenticulaires, avec mamelon central plus
ou moins développé.
Lepidocyclina insulz-natalis, J. et (ne TAG 13 siKEB aE PA, 8}:
Orbitoides (Lepidocyclina) insule-natalis R. Jones et Chapman, in Andrew’s
Christmas Island (1900), 242, Pl. XX, fig. 5, non Schlumberger.
Orbitoides de grande taille, atteienant 32 millimétres de diamétre,
minces, 2 peine mamillés au centre. la surface est couverte de petites
granulations ayant de 0.15 4 0.20 millimétre de diamétre, quadrangu-
laires ou pentagonales. Dans la partie centrale, elles arrivent souvent
4 se toucher et elles entourent alors les logettes. C’est bien 1a le carac-
tére de cette espéce comme il a été indiqué précédemment.
Localités. Cette espéce a éte recueillie au Barrio de Mesaba (Cebt,
n° 272) (figs. 1, 2), ume variété (fig. 3) provient de Guila-Guila (Cebu,
n° 278) ot elle est associée aux espéces suivantes; une coupe mince de
cette derniére forme communiquée par M. Warren D. Smith a été repro-
duite Pl. A, fig. 7, avec un grossissement de 10 fois.
Lepidocyclina richthofeni Warren D. Smith. PI. C, figs. 1, 2, 3.
Lepidocyclina richthofeni Warren D. Smith, Philip. Journ. Sci. (1906) 1,
203.
J’ai indiqué plus haut les caractéres assez peu précis de cette espéce:
forme lenticulaire, logettes latérales séparées par des cloisons épaisses
et absence de piliers ou piliers peu développés. Je réserverai cette déno-
mination pour les formes voisines de l’espéce précédente, mais avec peu
ou point de piliers.
On retrouve ces caractéres dans les échantillons de la vallée de Cuma-
jumayan (Pl. C, fig. 3) (Cebu, n° 285); ils sont lenticulaires, mais
moins gros que le type, qui est du reste indiqué comme le plus grand
échantillon trouvé 4 Binangonan; leur diamétre ne parait pas dépasser
25 millimétres avec une épaisseur de 6 millimetres. Les piliers sont
peu développés et seulement dans la partie moyenne; vers le centre on
mobserve guére que des cloisons épaissies rappellant celles de L. formosa.
Seulement le réseau est bien plus serré et les logettes sont bien plus
petites ; elles se rapprochent beaucoup par leurs dimensions de celles des
especes précédentes.
Des échantillons trés analogues ont été recueillis pres de la mine de
Compostela (Cebu, n° 289).
A Guila-Guila (Cebu, n° 278) les Lépidocyclines sont de forme un
peu différente; elles sont généralement minces et assez fortement mamil-
lées: les unes (Pl. C, fig. 2) ont seulement 20 4 22 millimétres de dia-
métre et présentent autour du mamelon central assez large un disque
42 DOUVILLE.
épaissi de 18 millimetres de diamétre, au dela duquel la coquille s’amin-
cit brusquement comme dans certains Orthophragmina (O. bartolomei
Schlm.). Le réseau superficiel est trés fin, les piliers sont 4 peine mar-
qués et les cloisons séparatives sont épaissies.
D’autres échantillons, et ce sont les plus nombreux (Pl. C, fig. 1, 1b),
sont plus grands et plus minces; ils atteignent 38 millimétres de dia-
métre, sont mamillés au centre ot leur épaisseur est de 3.5 millimetres.
La partie moyenne présente quelques piliers analogues a ceux de l’espeéce
précedente; mais au centre les piliers disparaissent ‘et les cloisons sont
plus ou moins épaissies. Ce caractére les distingue du L. insule-natahs,
ou les piliers sont au contraire plus développés dans la partie centrale.
2° Formes globuleuses avec collerette équatoriale.
Lepidocyclina formosa Schlumberger. Pl. D, figs. 2, 3, 4, et 5.
Lepidocyclina formosa Schlumberger, Samml. d. Geol. r. museums in Leiden,
(1900), I, 6, fase. 3, 128.
Espéce de grandeur moyenne atteignant un diamétre probablement
supérieur 4 12 millimétres lorsque la collerette est bien entiére. la
partie centrale est globuleuse, presque sphérique; elle mesure ordinaire-
ment 6 millimétres de diamétre avec une épaisseur de 4.5 a 6 millimeé-
tres. Au dela le bord s’amincit brusquement et forme dans la région
équatoriale une sorte de collerette toujours plus ou moins brisée; la plus
grande largeur que j’ai observée est de 3 millimétres, mais celle-ci devait-
étre notablement plus grande (Pl. D, fig. 1 et 2).
Cette espéce est nettement caractérisée par lépaisseur des cloisons qui
entourent les logettes latérales; la surface parait lisse et les piliers sem-
blent faire défaut ainsi que les granulations superficielles qui leur cor-
respondent (Pl. D, fig. 3). L’épaisseur des cloisons peut atteindre 0.15
4 0.20 millimétre pour un diamétre de logettes légerement supérieur. On
observe du reste d’assez grandes variations dans ces dimensions et d’ordi-
naire les logettes sont plus grandes vers le milieu de la coquille.
Localités.—Cette espéce est trés abondante prés de la mine de Com-
postela (Cebu, n° 287) ow elle est associée 4 Lep. richthofent et a Vespece
suivante ; elle a également été recueille 4 Guila-Guila (Cebu n° 278) ou
elle accompagne les variétés plates de l’espéce précedente.
Lepidocyclina inermis sp. noy. Pl. D, fig. 5.
On recontre prés de la mine de Compostela des échantillons ayant la
méme forme que L. formosa, globuleux et bordés d’une collerette. Ils
sont dépourvus de piliers comme cette espéce, mais les cloisons sont tou-
jours minces; ils correspondent au stade n° 0, défini plus haut.
LES FORAMINIFERES. 73
B. Section des Nephrolepidina.
Formes petites, lenticulaires, plus ou moins renflées; logettes ogivales ;
deuxiéme loge réniforme.
Lepidocyclina smithi sp. nov.
Les calcaires a Nummulites de Vile de Batan renferment des Orbi-
toides de 3 a 5 millimetres de diamétre,
qui ne sont guere connues que par leurs
sections. J’ai pu cependant isoler une de
ces formes qui présente les caractéres des
Nephrolepidina.
Elle a 4 millimétres de diamétre et a sa
surface on distingue 4 trés grosses pustules
qui viennent presque se rejoindre en laissant
seulement entre elles 4 trainées de logettes
qui dessinent une sorte d’X. En usant y
progressivement l’une des faces j’ai pu con- ae Gat nes eee ae
stater que les pustules en se rapprochant Pla", Gquatoriay phos auatre
du plan équatorial, prenaient leur forme Piliers médians, gr. 20 fois.
ronde habituelle. a couche équatoriale présente les logettes rhom-
boidales caractéristiques. C’est une forme microsphérique.
Cette Lépidocycline provyient d’une couche de calcaire intercalé dans le
systéme lignitifére (échantillon n° 2).
Une préparation d’un calcaire de Vile de Batan (baie de Calanaga n°
4) dans lequel on observe de nombreuses Nummulites 4 test noir, montre
la section verticale d’un Orbitoides avec 2 grosses pustules d’un cdté et
une de l’autre, mais c’est mégasphérique. C’est peut-étre la forme A
correspondant a Vespéce précédente.
Le type trés particulier que je viens de décrire correspond a certaines
variétés de la L. premarginata d’Kurope. Hlle se distingue de cette
espéce par ses 4 grosses pustules trés rapprochées ; elle rappelle également
L. ferrerot, mais dans cette derniére les pustules sont beaucoup plus
éloignées et donnent 4 la coquille une forme étoilée.
Lepidocyclina verbeeki N. et H. PI. D, fig. 8.
Orbitoides papyracea Brady, Geol. Mag. Dec. II (1875), 532, Pl. XIV, fig. 1,
non Boubée.
Lepidocyclina verbeeki Newton et Holland, Ann. & Mag. Nat. Hist. (1899),
VII, 3, 257, Pl. IX, fig. 7, Pl. X, fig. 1.
Les formes types caractérisées par quelques pustules de grandeur
moyenne sont assez rares. la figure 8 reproduit un de ces échantillons
partiellement engagé dans la roche. I] provient du Calcaire blane
74 . DOUVILLE.
supérieur de Cotabato Valley (ile de Cebu, n° 279) ot il est associé a la
forme suivante et aux Miogypsina.
Lepidocyclina inflata Provale. Pl. D, fig. 6 et 7.
Lepidocyclina tournoueri var. influta Provale, Riv. italiana in Erlleorigieete.
Ann, XV (1909), 73, Pl. III, figs. 14, 15.
C’est une forme voisine de la précédente, mais qui s’en distingue par une
trés grosse pustule centrale, tantdt seule, tantdt entourée de pustules plus
petites. C’est de beaucoup l’espéce la plus fréquente dans les calcaires
blancs supérieurs de Pile de Cebti. C’est peut-étre une simple variété
de Vespéce précédente.. Ce groupe de formes mégasphériques represénte
dans la province orientale celui du Lep. tournoueri, dont il se distingue
par ses logettes équatoriales plus petites.
Lepidocyclina cf. marginata Mich.
Nummulites marginata Michlotti, Saggio Storico dei rizopodi caratteristici
dei terreni Sopracretacei (1841), 45, Pl. III, fig. 4.
Lepidocyclina marginata Lem. et. R. Douv., Sur le genre Lepidocyclina, Mem.
Soe. geol. Fr. Paleont. (1904), 12, 16; Rob. Douvillé, Sur des Lepido-
cyclnes nouvelles. Bull. Soc. géol. Fr. (1907), IV, 7, 307, Pl. X, figs.
1G A es,
Les formes précédentes mégasphériques sont accompagnées d’une forme
plus rare, un peu plus grande et microsphérique; elle présente de nom-
breuses pustules peu saillantes séparées par des logettes 4 parois épaisses
et son diamétre atteint 7 millimétres. Mais les matériaux a ma disposi-
tion étaient insuffisants pour en permettre une description complete, et je
Vai considérée provisoirement comme une race du Lep. marginata. ©
- Genre MIOGYPSINA.
Miogypsina irregularis, race orientalis. Pl. D, fig. 9 et 10.
Nummulites irregularis Michelotti, Saggio Storico die rizopodi caratteristici
dei terreni Sopracretacei (1841), 45. _
Miogypsina irregularis Sacco, Bull. Soc. belge de Géologie, (1893), 7.
Flabelliporus orbicularis Dervieux, Atti d. R. Acad. delle Scienze di Torino,
(1893), 29
Miogypsina irregularis Schlumberger, Bull. Soe. géol. de France (1900), Iii,
28, 328, Pl. II, figs. 1 4 7.
Cette forme est abondante dans les calcaires planes supérieurs de Vile
de Cebu; elle est trés yoisine de Vespéce d’Hurope dont elle différe seule-
ment par ses gros granules plus espacées et occupant une plus grande
partie de la surface.
Quelques échantillons plus petits ont été trouvés dans les calenives
tendres jaundtres de Gaba Bay (ile de Batan, n° 8) -situés bien aw
dessus des couches charbonneuses; ils sont associés au Cycloclypeus et a
des Amphistégines.
LES FORAMINIFERES. 75
Genre AMPHISTEGINA.
Trés commun dans toutes les couches.
Amphistegina niasi Verbeek.
Nummutlites Niasi I Verbeek, Verbeek et Fennema, Deser. geol. de Java et
Madoura (1896), 1155, Pl. TX, figs. 120-122.
Dans les calcaires 4 Nummulites du systéme charbonneux de l’ile de
Batan.
Amphistegina cf. mamillata d’Orbigny. :
Hspéce de petite taille, ayant environ 1.5 milli-
métre de diamétre; le cété visible ressemble tout
a fait & la figure qui a été donnée par Carpenter
(Intr. pl. XIII, fig. 23); les différences dans le
mode de terminaison des loges de la face infé-
rieure tiennent peut-étre 4 un meilleur état de
conservation.
Localité.—Couche a Cycloclypeus communis de pig 9. amphistegina cf.
Vile de Batan (Gaba bay). mamillata, del’ fle de
Batan, gr. 20 fois.
RESUME ET CONCLUSIONS.
D’aprés V’étude qui précéde on peut classer de la maniére suivante les
échantillons communiqués :
I. Terrain eogéne (comprenant l’éocéne et Voligocéne) Stage Stam-
plen.
Calcaire de Caracaran (ile de Batan,?" éch. n° 2).
O’est un calcaire gris bleudtre, sur lequel les Foraminiféres se déta-
chent en noir; il fait partie du systéme lignitifére et il est indiqué comme
intercalé entre les couches de lignite.
Les plaques minces et les sections polies ont montré de petites Num-
mulites de 2.7 millimétre de diamétre, qui paraissent correspondre a NV.
niasi Verbeek; mais cette derniére espéce étant microsphérique, celle des
Philippines, qui est mégasphérique, a du étre distinguée comme NV. sub-
niast. Le méme calcaire renferme montre Amphistegina niasi Verbeek,
Polystomella sp. et une curieuse Lepidocyclina de la section des Neophro-
lepidina, L. smitht, qui rappelle certaines variétés du L. proemarginata.
La coexistence des Nummulites et des Lépidocyclines caractérise le
Stampien; il est 4 remarquer que ces deux genres ne sont représentés
ici que par des formes de trés petite taille, tandis qu’un peu plus au
sud, 4 Bornéo, les grandes formes abondent.
IL, Terrain Néogéne (aquitanien, burdigalien, helvétien, etc.) Htage
Aquitanien.
* The Coal Deposits of Batan Island par Warren D. Smith, 1905 (Bull. No. 5,
the Mining Bureau, Manila).
76 DOUVILLE.
1° Grés tendre jaunatre de Sibud Gulch (old Alpaco Mine, ile de
Cebu,?® éch. n° 273).
La roche est d’une faible dureté et le ciment calcaire est trés peu abon-
dant; les fossiles y sont 4 état d’empreintes et les caractéres internes
sont tres difficiles a reconnaitre. la faune se compose essentiellement
@Orbitolites et d’Alveolinella; il faut ajouter Operculina costata, var.
tuberculata, Rotalia, Polystomella. Cette couche est indiquée comme
supérieure au systeme lignitifére et inférieure aux calcaires 4 Lépidoey-
clines. lle serait ainsi 4 peu prés au niveau des couches 4 Orbitolites
et Alveolinella de Java que M. Verbeek place dams son étage m, c’est-a-
dire dans l’Aquitanien inférieur. Mais par suite de la conservation
insuffisante des fossiles, cette attribution doit étre considerée comme seule-
ment provisoire. I] faut ajouter que M. le professeur Martin a signale 2°
des Orbitoides trouvées par Semper dans une marne d’Alpaco.
2° Le niveau le mieux caractérisé est celui des calcaires 4 grandes -
Lépidocyclines :
“Caleaire de Guila-Guila (Cebu, n° 278) ; il renferme de nombreuses
Lépidoeyclines de grande taille; les unes présentant des tubercules bien
développés sur toute leur surface, ont été rapportées 4 L. insule-natalis,
tandis que les autres, dépouryues de tubercules ont été assimilées a L.
richthofeni; ces deux formes sont du reste trés voisines; elles sont as-
sociées a une troisiéme espéce beaucoup plus petite, composée d'une
partie centrale trés renflée bordée par une sorte de collerette; c’est la
L. formosa, dépourvue de tubercules, mais présentant entre les logettes
des cloisons trés épaisses. Ces diverses formes se trouvent assez souvent
dégagées.
Il faut places au méme niveau les calcaires du Barrio de Mesaba
(Cebu, n° 272), avec L. insule-natalis, ceux de la vallée de Cumaju-
mayan (Cebu, n° 28) avec L. richthofem et L. formosa et deux qui affleu-
rent prés de la mine de Compostela (Cebu, n° 289) avee ces deux mémes
espéces et une troisieme voisine de L. formosa mais ne présentant entre
les logettes que des cloisons minces, c’est L. inermis.
3° Il faut placer probablement 4 un niveau un peu plus élevé, un
échantillon de caleaire tendre d’une couleur blanc-créme recueilli dans les
grands escarpements, le long de la route de Toledo (Cebu) sur les bords
de la riviére Minanga (éch. n° 277, pres du Camp n° 1) ; il présente sur
sa surface des échantillons bien conservés d’Operculina complanata et de
Cycloclypeus communis; cet échantillon rappelle les marnes 4 Silex de
VPAquitanien de Bornéo.
Ktage Burdigalien.
7*Ceba Island par Warren D. Smith. This Journal (1906), 1, 1043. The
Geology of the Compostela Danao Coal Field, par le méme, Ibid. Sec. A, (1907)
2, 377.
» Orbitoides von den Philippine, Centralbl. f. Mineral., Geol. u. Paléon. (1901),
326.
LES FORAMINIFERES. Th
Ce niveau supérieur est caractérisé par Vapparition des Miogypsina et
Pabondance des petites Lépidocyclines du groupe de L. (Nephrolepidina)
verbeekt. Je lui rapporte les deux échantillons suivants:
Un ealeaire sableux jaunatre, trés tendre de Gaba Bay, dans Vile de
Batan (éch. n° 8), indiqué comme affleurant bien au dessus du systéme
lignitifére; il renferme des Foraminiféres bien conservés, mais trés
fragiles, parmi lesquels Globigerina, Cycloclypeus communis, Amphiste-
gina cf. mamillata, et de petits Miogypsina, ces derniers rappelant tout
a fait les formes du Burdigalien des environs de Dax.
Un caleaire blane assez tendre, qui couronne la Cordillére centrale
de V ile de Cebu, dans la Vallée de Cotabato (éch. n° 279): il renferme
L. verbeeki, déja signalé par M. Warren D. Smith, mais surtout LD.
inflata associé 4 de nombreuses Miogypsina irregularis. :
Des trois faumes que je viens de signaler, la seconde caractérisée prin-
cipalement par Vabondance des grandes Lépidoeyclines a une extension
considérable depuis Madagascar jusqu’aux Philippines. J’ai fait voir
dans mon Etude sur les Foraminiféres du Tertiaire de Bornéo *° qu’elle
correspondait a PAquitanien; j’y ai distingué trois niveaux E, F, G,
qwil sera peut-étre possible de retrouver aux Philippines, quand les ex-
plorations géologiques y seront plus avancées.
Le niveau supérieur Burdigalien H, présente aussi une grande ex-
tension; il est trés développé dans Vile de Nias, 4 Java, d’ou pro-
vient le type de LZ. verbeeki, et 4 Bornéo ot je n’avais pas distingué
cette espéce de la forme européenne voisine (Ll. towrnouert). Ce méme
niveau parait se prolonger au Nord a Formosa (Taiwan) et au Ja-
pon au environs de Tokyo. Cette dernicre localité n’atteimt encore
que la latitude de 36°, c’est-a-dire a peu pres celle de Gibraltar, tandis
que les Lépidocyclines atteignent en France presque le 44° degré, et
dépassent en Italie le 45°.
Le tableau suivant résume les rapprochements que je viens d’indiquer:
—
Philippines. Bornéo.
CENGEETCS SERS NEES a petites _| Lep, Verbeeki, Miogypsina Benne a. BURDIGATLEN!
Lépidocyclines _-____-------__- Cycloelypeus communis —-_----_--____
Calcaires moyens_______----__- eee communis -__--.------- Ne.
Il. Operculina complanata______----____
3 AQUITANIEN.
Lep. insulée-natalis ______----________ F. 8
eps Richthotentes=—= === enc eeee
‘Lépidocyclines --...-_-___-___- he ps OFM OSty= = so eee te,
Calcaires inférieurs 4 grandes_ {
Nummulites Subniasi __
Amphistigina Niasi ____
Lépidocyclina Smithi___.----_-______
ire Inférieur 4 Nummulites_
I. Systéme lignitifere et calca-
D. Stampien.
* Bull. de la Soc. géol. de France, 4 Série, t. V, p. 43.
78 DOUVILLE.
En Europe la sucession des faunes est trés analogue: les Lépidocyclines
y sont trés développées dés le Stampien aussi bien en Espagne qu’en
Italie, elles y atteignent une grande taille et y sont associées comme 4
Bornéo avee des Nummulites réticulées. Le groupe du ZL. dilatata rem-
place le groupe Asiatique du L. insule-natalis et se prolonge dans Aqui-
tanien, tandisque dans les niveaux supérieurs le groupe du L. towrnowert
remplace celui du L. verbeekv; tous les deux sont associées aux Miogyp-
sina.
Le bassin européen et le bassin asiatique paraissent avoir été compléte-
ment séparés dés la fin de ’Hocéne par le soulévement du Liban qui
s’est développé en travers de la Mésogée et a séparé la Mediterranée de
VPOcéan Indien. C’est seullement 4 une époque beaucoup plus récente
qui ouverture de la mer Rouge a été sur le point de rétablir, une com-
munication entre les deux mers, mais les eaux de l’Océan Indien ont été
arrétées a quelques kilométres de la Méditerranée devant la faible bar-
riére de V’isthme de Suez.
TABLE DES MATIERES.
Alveolinella ‘ mamillata (Amphistegina)
Amphistegina marginata (Lepidocyclina)
andrewsiana (Lepidocyclina) martini Schl. (Lepidocyclina)
angularis (Lepidocyclina) j martini W. Smith (Lepidocyclina)
angulosa (Lep. tournoueri var.) - martini (Orbitoides)
borneénsis. (Lep. tournoueri var.) -multipartita (Lepidocyclina)
carteri (Lepidocyclina) murrayana (Lepidocyclina)
communis (Cycloclypeus) neodispansa (Lepidocyclina)
complanata (Operculina) Nephrolepidina
Cycloelypeus ngembaki (Lepidocyclina)
ephippioides (Lepidocyclina) niasi. (Amphistegina )
Eulepidina Nummulites
ferreroi (Lepidocyclina) Operculina
formosa (Lepidocyclina) Orbitolites
gallienii (Lepidocyclina) Polystomella
gigantea (Lepidocyclina) : provalei (Lepidocyclina)
Heterostegina radiata (Lepidocyclina)
inermis (Lepidocyclina) =~ --richthofeni (Lepidocyclina)
inflata (Lep. tournoueri var.) Rotalia - ;
inflata ( Lepidocyclina) smithi -(Lepidocyclina)
insule-natalis (Lepidocyclina) subniasi (Nummulites)
irregularis (Miogypsina) . sumatrensis (Lepidocyelina) .
joffrei (Lepidocyclina) BSE tournoueri (Lepidocyclina )
Lepidocyelina ; verbeeki (Lepidocyclina)
Fie. 1.
. Orbitolites. Méme provenance, gr. 10 fois.
. Operculina costata d’Orbigny. Minanga river (Cebi, N° 277), gr. 10 fois.
. Operculina costata var. tuberculata. Ola Alpaco Mines (Ceba, N° 273)
Fic.
Fie.
Fie.
Nn
or}
© %
. Méme espéce de la méme localité, Section mince
EXPLICATION DES PLANCHES.
PLANCHE A.
Alweolinella. Old Alpaco Mines (Cebt, N° 273), gr. 10 fois.
gr. 10 fois.
. Cycloclypeus communis Martin. Minanga River (Cebfi, N° 277) gr. 10
fois.
. Heterostegina. Barrio of Mesaba (Ceba, N° 272) gr. 10 fois.
. Lepidocyclina insule-natalis J. et Ch. Guila-Guila (Ceba, N° 278) x 10,
@aprés une préparation de M. Warren D. Smith.
PLANCHE B.
. Lepidocyclina insule-natalis J. et Ch. Barrio of Mesaba (Ceba, N° 272).
(la) Profil en vraie grandeur; (1>) surface grossie 10 fois; le milieu
vers le haut 4 gauche a été légerement usé.
. Méme espéce, de la meme localité, grandeur naturelle.
. Lepidocyclina insule-natalis J. et Ch. Guila-Guila (Cebi, N° 278). (3 et
3a) En grandeur naturelle; (3>) surface du méme échantillon grossie
10 fois.
: PLANCHE C.
. Lepidocyclina richthofem Warren D. Smith. Guila-Guila (Cebi, N° 278),
grandeur naturelle. (1b) Surface du méme échantillon grossie 10 fois.
. Autre échantillon de la méme provenance beaucoup plus épais et avec
un commencement de collerette.
. Lepidocyclina richthofeni. Cumajumayan Valley (CebG, N° 285), détail
de la surface, gr. 10 fois.
PLANCHE D.
et 2. Lepidocyclina formosa Schlumberger. Compostela Mine (Cebti, N°
289). Vues de face et de profil en vraie grandeur.
. Méme espace de Guila-Guila (Ceba, N° 278), détail de la surface gr. 10
fois.
gr. 10 fois, d’aprés une
préparation de M. Warren D. Smith.
Lepidocyclina inermis H. Douvillé. Compostela Mine (Ceba, N° 289) gr.
10 fois.
ét 7. Lepidocyclina inflata Provale. Cotabato Valley (Ceba, N° 289), gr.
10 fois.
Lepidocyclina verbeeki Newton et Holland. Méme provenance, gr. 10 fois.
et 10. Miogypsina irregularis Michelotti, race orientalis. Méme_ prove-
nance, gr. 10 fois.
80
Fic. 1.
2.
P DOUVILLE.
FIGURES DANS LE TEXTE.
Nummulites subniasi sp. nov. de la formation charbonneuse de Vile de
Batan, gr. 10 fois.
Lepidocyclina swmatrensis, gr. 6 fois d’aprés la figure originale de Brady.
2bis, Section d’un echantillon de Vile de Nias, gr. 10 fois.
3.
4.
Lepidocyclina carteri Martin, disposition des piliers prés de la surface,
gr. 20 fois.
Lepidocyclina gigantea Martin, disposition des piliers prés de la surface,
gr. 20 fois. :
. Reproduction grossis 5 fois de la partie centrale de la figure type de MM.
Rupert Jones et Chapman, le grossissement de cette derniére figure
nest pas indiqué. :
. Lepidocyclina formosa, disposition des logettes sur une section de l’échan-
tillon type de l’espéce, gr. 20 fois.
. Lepidocyclina gallienti de Madagascar; coupe prés de Ja surface montrant
la disposition des piliers, gr. 20 fois.
. Lepidocyclina smithi; coupe prés de la surface paralléle au plan équatorial,
montrant le grand développement des quatre piliers médians, gr. 20
fois.
. Amphistegina cf. mamillata de Vile de Batan, gr. 20 fois.
DOUVILLE: LES FORAMINIFERES. | (PHIL. JOURN. ScI., Vou. VI, No. 2.
PLANCHE A.
DoUVILLE : LES FORAMINIFERES.}
PLANCHE B.-
[PHiu. Journ. Scr., Vou. VI, No. 2.
NS eee
DouvILLe: LES FPORAMINIFERES. | (PHIL. JouRN. Scr., Vou. VI, No. 2.
PLANCHE C.
DOUVILLE : LES FORAMINIFERRS. ]
PLANCHE D
[Pri. Journ. Scr., Vou. VI, No. 2.
THE PHILIPPINE JOURNAL OF SCIENCE,
D, General Biology, Ethnology and Anthropology.
Vol. VI, No. 2, April, 1911.
THE HARVEST FEAST OF THE KIANGAN IFUGAO.
By Roy FRANKLIN BARTON.
The Ifugao has some hundreds of spirits of various ranks ranging
from gods to demons, monsters, imps, and spirits dwelling in trees and
stones; and in addition to these, there are the souls, linawwa, of his
ancestors, who are nearly as powerful as the other spirits. A very large
share of the Ifugao’s life is spent in obtaining animals and other things
needed for religious feasts.
Whenever a member of the family falls ill, chickens, ducks, pigs, or
a carabao, according to the wealth of the family and the seriousness of
the case, are killed; one or more jars of rice wine and a quantity of
betel nuts and betel leaves are provided. An enormous number of spir-
its, including all the spirits of the ancestors for six or seven genera-
tions, and the ancestral spirits in a direct male line from Bugan and
Balitok, the survivors of a great flood, are invited by name to the feast.
Tf an Ifugao leaves on a journey far from home; if he enlists in the
Constabulary; or cuts his son’s hair for the first time, he makes a reli-
_ gious feast. If he happens to go to Nueva Vizcaya to buy a carabao,
he makes a feast to which he invites certain spirits, praying to them to
put it into the mind of whomsoever he may try to buy from, to sell the
animal cheap. If an Ifugao marries or is divorced; if a child is born
to him; if he makes a loom; if he becomes angry with a man of another
village and desires his death; if he moves into another house; if he is
apparently unsuccessful in a love affair; if he finds that he is consuming
his supply of rice too rapidly; if a bird called pitpit flies into his house ;
if he names his baby; if a bad debtor delays payment—a proper feast is
the invariable accompaniment.
Certain feasts rank higher in importance, expense, and pretentiousness
than others. The most expensive and the one which invests the giver
with great prestige is the uyaue,! the feast of the kadanyyan, a class of
rich men that approaches an aristocracy. The kolating, or harvest feast,
*In writing Ifugao words in this article, a phonetic system of spelling is used.
It may be noted that the vowels have the Continental values and that the g is
always hard.
81
82 BARTON.
is not very expensive; it can be given for from fifteen to twenty pesos;
it is not pretentious, for every one who has a few rice fields gives it; but
it is of the greatest importance.* When the meaning of rice to the Ifu-
gao is considered, it is not strange that harvest time should be celebrated
by feasts having profound religious importance. A bad rice crop indi-
cates that the spirits have a “bad mind” toward the village and special
effort must be made to appease them to the end that further disasters
may be averted. A good rice crop is an occasion for a thank offering,
and for a feast to keep the spirits right during the coming year. .
Every man who owns a granary, alang, must give a ceremonial feast,
baki.2 If his granaries are located in different places, the man must
give a feast at each. These have a fourfold function: First, to thank
the deities, bagol, for the crop of the past year if it has been good, or
to reprove them gently and argue the case with them if it has been a
bad one; second, to persuade the deities to increase the rice as it is being
cut and stored in the granary; third, to induce them not to decrease the
rice nor to destroy it during the year, as, for example, by strong winds
that can break granaries, or by lightning; and fourth, to put the deities
in a “good mind,” that they may favor the general welfare of the village
during the year to come, that they may make sickness rare, prevent de-
structive storms, defeat enemies should enemies come, frustrate the
designs of sorcerers in other villages, and make women, pigs, and chickens
fertile.
The second function-of the harvest feast, to persuade the deities to
increase the rice as it 1s being cut and stored, is especially interesting.
The idea seems absurd, but it must be considered that these people have
no experience contrary to this belief; for, even if they count the mano-
jos * of rice, butek, when they put them in the granary,’ they do not
keep track of the number taken from the granary for daily use. The
Igorots of Lepanto also believe that the divinities may increase the rice
as it is being cut and stored away. But the most intelligent Ifugaos
deny the belief in this form, They believe that the divinities may make
*In this paper the writer desires to be understood as speaking of the Ifugaos
who live in the village of Kiangan. The customs and practices of the various
divisions of the Ifugao tribe vary somewhat and this article would be inaccurate
did it pretend to apply to the Ifugaos as a whole. :
’ Baki is the general term for a religious feast. All feasts of the Ifugaos
have some religious significance. !
“Small hand sheaves of headed rice. From the Spanish manojo, a bundle of
herbs or other plants that can be held in the hand. i
5 Counting the manojos is, except in the case of a field that is let to a renter,
tabooed on the ground that the bagol will not miraculously increase the manojos
if they be counted. There is, among some card players, the vague remnant of
a belief that if a hand be not picked up until the deal is finished, the cards
will grow to higher denominations.
HARVEST FEAST OF THE KIANGAN IFUGAO. 83
the rice sufficient, whereas it would not have been sufficient without
their action.® This, of course, is only a vaguer form, a toning down of
the old belief, made necessary by a growing intelligence.
The kolating is always celebrated on the day on which the owner of
the alang begins to cut his rice. In the early morning before either
harvest or feast commences, the owner of the fields kills a chicken and
examines its gall bladder for an omen as to whether or no the time is
propitious for the harvest. A full, black bladder is a favorable sign in
this case, as in others in which the gall bladder is examined for an
omen, as, for example, in cases of sickness or departure on a journey.
Unless the chicken is diseased, the gall bladder is always full early in
the morning at which time the digestive organs have for some hours
rested from their functions. If, by chance, the gall bladder is white, or
empty, the harvest and feast are postponed for two or three days, when
the omen is consulted again.
The harvest feast takes place at the granary. The doors of the latter
are decorated with leaves of the haganyga tree and with hagaga, a kind
of grass common in rice fields, similar to what is called “nut-grass” in
some parts of the United States. These decorations are said to frustrate
malicious human sorcerers and other enemies in their efforts to make
the rice disappear rapidly and to decrease it in quantity.
The feast begins at about 10 o’clock in the morning. The dotal,"
a kind of a mat made of long runo stems laid closely parallel and tied
together with rattan, used on festive or funeral occasions, is brought
from the granary, unrolled, and placed on the ground underneath the
structure for the people to sit on. The mat fits the space under the gran-
ary. Bubud jars, augang, generally two, holding from fifteen to thirty
liters each, are set in the center of the mat. These jars contain the
fermented rice, the malt called bubud, and the binabudan, or rice wine,
called tapui in Benguet, and tafei in Bontoc. Sometimes the rice wine
is termed binadayan, but binadayan and baya are generally terms for
intoxicants and apply to the bas: and gin of the Christian Filipinos and
the whisky of the Americans. Usually, there are about four and one-
half liters of the beverage in an average-sized bubud jar; the rest is
malt. Wooden bowls are provided into which the binabudan is strained
from the bubud jars by means of three or four round stalks which hold
°There‘is a feast called humangali page given every year by such persons as
find the rice in their granaries being consumed more rapidly than they think
it should be. Last year, 1909, a partially Christianized Ifugao, one of the
municipal offieials, refused to give the harvest feast. When, after about three
months, he found that his supply of rice was being used up too fast, he gave
this feast hoping to mend matters.
7 Dotal is the ordinary Ifugao word for floor. It is applied to the mat here
referred to because the mat is used at the feast to make a floor.
84. BARTON.
the malt back in the jar. The rice wine is dipped up from these wooden
bowls by means of coconut shells, tawg, the rims of which have been
notched to fit the mouth. Wooden troughs, timgap, are filled with betel
nuts and betel leaves.§ In one trough are some twelve to twenty stones
called buga.? Whenever an animal is killed at the granary some of its
blood is smeared on each of these stones, the person smearing it saying:
“Thou, blood stone, do not get lost.”2° Three or four palipal, or bamboo
clappers, are placed in the trough with the buga. The palipal is essen-
tially a partially split stick of bamboo about fifty centimeters long, the
halves of which clap sharply together when it is shaken. A large flattish
basket of cooked rice, hinamar, is provided for the linawwa. According
to the Ifugao, everything living or dead has an invisible, immaterial
shadow, and it is this shadow that the linawwa use. After repeated
investigations I have been unable to find any term for this shadow.
When hard pressed for a name two or three men have called it the
linauwa ; but a lanauwa, strictly speaking, is the soul of a man, an animal,
or a plant. At any rate, it is a convenient provision of the Ifugao reli-
gion that the spirits use the invisible, immaterial, part of the rice wine,
betel nuts, blanket, bolo, or other offering, leaving the material part for
the consumption or use of the living. After all these things, bubud,
betel nuts, betel leaves, cooked rice, palipal, and blood stones, have been
placed in the center of the mat, the people take their places, squatting ”
in a ring about them.
Let us look at the principal actors in the ceremony about to begin.
There are twenty men and three women present, this being about the
usual ratio of the sexes represented at these feasts, and any number of
small boys and girls. The larger children are busy in the rice fields.
Occasionally, however, one of the large boys who is carrying rice to the
granary remains for a few minutes to watch the ceremonies, and to
rest after climbing the steep hillside. A typical feast will be described.
® The betel nuts are kept in the troughs from year to year. In some of the
prayers of this feast the rice is called on to become hard and dry in imitation
of the betel nuts. It is told to “follow” the betel nuts, which stay in the granary
from year to year; not to be eaten up; not to disappear, but to have a portion
left at the next harvest.
®The following is the story of the buga: Alingdayu, the place spirit of Naga-
dangan, used to eat gold. In his stomach the gold turned to stone. He gave
this stone to Balitok, the Ifugao Noah, who, with his sister Bugan, survived a
flood that drowned all other people. Alingdayu told Balitok that so long as he
kept the stone he would have good crops. Balitok put other stones with this
original stone and these others acquired its properties. He gave them to his
children and they have added to the number according to the demands of the
increased population.
10 He’a, buga, adika mondekela.
HARVEST FEAST OF THE KIANGAN IFUGAO. 85
The granary belongs to Kodamon, one of the richest men in Kiangan
and a typical representative of the upper class Ifugao, the kadartyyan.™
He is tall, well proportioned, and of middle age. He admires the white
man and respects him; but his tribal pride, together with a most ad-
_mirable sense of the fit and harmonious, holds him, it has often seemed
to me, true to the religion and life of his fathers. He apes neither the
white man nor the Christian Filipino. It is as if he preferred to remain
(and this in contrast to certain of his fellow kadaryyan) a good Ifugao
rather than become a “half-and-half.” He knows, as an Ifugao hadang-
yan ought to know, all his ancestors, male and female, for six or seven.
generations, and can trace his genealogy in a direct male line to Bali-
tok, the Ifugao Noah. His two sisters and his wife are nearly of his
age. They are vigorous appearing women who have worked hard in
their time, but now have daughters to take their places in the rice fields.
Gimbungan, Kodamon’s father, is a very old man, almost blind. No
one in the region is better versed in the Ifugao folklore and religion than
Gimbungan. His faculties, however, are waning. Whenever he starts
an invocation, or phase of ceremony, he goes through it like an automaton,
and immediately repeats it again and again until Kodamon starts him
off on something else, a task performed respectfully and with evident
filial love. JXodamon has carried Gimbungan’? a distance of over 3
Kilometers from Longa to Pindungan, where the feast is to be held; for
the old man is too feeble to walk so far. Hight or nine middle-aged or
elderly cousins, and a pig, complete the list of those who take a leading
part in the ceremony.
The younger men** play the parts of acolytes and exhorters; they
strain the rice wine, hold the cup for the old men who are praying, hand
them palipal or whatever else may be needed. Not knowing the proper
* Padre Juan Villaverde applies the term nobility to this class. This Journal,
Sec. A (1909), 4, 241.
* As this is being written, Gimbungan is afflicted with a derangement of the
faculties of speech. He has directed Kodamon to find a dog to be killed at a
feast; he says that a dog is the proper animal to cure this particular affliction.
It may be that he has had a dream to that effect, or it may be that this belief
is due to the fact that the dog has more powerful and versatile vocal organs
than any other animal known to the Ifugao. Judge the dilemma in which
Kodamon finds himself. He would like to obey, it his duty to obey his old
father; but for an Ifugao kadargyan to eat dog! It would never be forgotten,
and years hence, in the drunken babbling around the bubud*jar, Kodamon would
hear of it! i
* By younger men I mean the younger middle-aged men, for no youths take
part in feasts.
101776——3
86 BARTON.
forms and the names of the deities, they exhort and call out phrases of
encouragement as the others pray or chant.
Oh! that’s it! Oh grant it! Come, ye deities! Take the pig, you deities!
Drink the rice wine! Make the rice heavy! Speed the harvesters!™*
These and other phrases the young men call out in a high, falsetto
voice as the ceremonies and prayers proceed. Those who perform this
office are called montobal, exhorters. I have been invited on several
occasions to join the young men in this, and on one occasion I accepted ;
but for an American to summon the bagol was, I thought, an unbecoming
and, in fact, a sacrilegious levity. However, the people did not regard
it as such. In fact, while the people are most sincere in their belief, their
religion has not yet reached that stage where ceremonies are conducted
with outward tokens of great awe, respect, and solemnity. It is the
pig, the betel nuts, the binadayan, and cooked rice that the bagol want,
not praise and long, grave countenances, for the deities are very mate-
rial in their desires.
The pig, with his feet lashed together, and a small pole passed between
them to hinder his struggles, is placed in front of the granary door near
the mat. (See Pl. II, fig. 2.)
The drum is the only musical instrument employed at the harvest
feast. Sometimes one is used, sometimes two. The drum is played in
double time. It accompanies nearly all the ceremonies.
All ceremonial circuits in the harvest feast are counterclockwise, begin-
ning at the east, in front of the door of the granary. The people say
that the bagol must have told Balitok and Bugan (the man and woman
who survived the great flood) to proceed so, and they believe that if a
man were to go around in the other direction he would surely fall off
a steep cliff in a journey, or else lose his way.
About the middle of the forenoon the people commence to drink rice
wine and invoke the linawwa of the monlapu. So begins the first part
of the ceremony.
The monlapu leaders in rice cultwre—Duldul, the mother of Santiago,
a rich man of Baai, is the monlapu of Kiangan disrict. That is to
say she is the one who decides when each phase of rice culture shall begin,
and takes the lead in each. She first begins spading, planting the seed,
transplanting, and harvesting. Until she has begun these things, no
one else may begin under penalty of misfortune, of bad crops, very likely
of death. Dulduli became the monlapu in response to a dream that came
soon after the death of the former monlapu. She is currently believed to
have eight years to reign in this capacity, when she will die. When
"Oh hia! Eh damit! Umalikayun bagol! Talim di babui dakayun bagol!
Ambayan di binadayan! Manangali page! Ikwadim di monagamid!
HARVEST FEAST OF THE KIANGAN IFUGAO. 87
she dies, she may inhabit, in the spirit, a tree or a boulder, or she
may become a new spring, as did the last monlapu in Ligaue. Some-
times the monlapw is a man. In case of bad crops the monlapw finds
himself universally blamed for them. He is considered to have been lax
in his religious duties.
As priestess of agriculture Dulduli makes feasts to ask in behalf of
the village for rain if it be needed or for relief from a rice pest that
may visit it. Just as in life she takes the lead in harvesting, spading,
planting, and so on, so after death, she (or he) is the first of all the
many spirits to be called to the harvest feast. All the monlapu who have
ever ruled Kiangan agriculture, together with the monlapu of neighboring
districts, are called to the feast.
Invocation of ancestors. Monamud.—tThe invocation and invitation of
the souls of the ancestors is, so far as my knowledge goes, the first part
of every feast of whatever kind, with the exception of the harvest feast
in which the monlapu precede. The ancestors are invited to be present
and to partake of the feast and drink the rice wine. (See Plate II.)
An old man should be able to name his ancestors, both male and female,
for at least six generations. Women do not usually know so many, but
they call on those whom they do know. Each man invokes his own
particular set of ancestors, and if none of his wife’s relatives be present,
her brothers or her father, he calls upon her ancestors too. In fact, he
looks upon his wife’s ancestors as his own in a way; and it is his duty
to have learned them from her father. Complimentary remarks are ad-
dressed to the ancestors, as, for example, this one that I once heard: -
“Brave ancestor, Ananayo, you who speared the child-slave to death.”**
Spirits of ancestors can not directly affect the harvest nor the growth of
rice, but they have the greatest influence with the spirits that do have such
power, and with the spirits that bring fortune and misfortune, children,
sickness, and death. They must never be slighted nor offended. Their
feelings are quite delicate, and if a man neglects his ancestors, they
will remove their watchful guardianship from him and misfortune of
some sort will result. The prayer to the ancestors is extemporaneous,
each man going about it in his own way. The word sai, long drawn
out, is used in the following invocation :
Thou, ancestor Ginnid, come, drink the intoxicant. There are betel nuts and
betel leaves here. Thou, ancestress Bugan, daughter of Oltagon, ete.”
* Mahwi Apo Ananayo, te timbuk, di himbut ud nate. Is this a reference to
the sacrifice of a slave at some early time?
* Sa-ai-ai-ai umali Apo Ginnid; umalika, wminum di baya. Tehtu momma
ut hapid. Sa-ai-ai-ai ka Apo Bugan, nak Oltagon, etc. In invoking the deities
the word sa-ai-ai-ai is sung in a peculiar long drawn chant. It does not appear
to have any meaning.
88 BARTON.
Rice wine is consumed at an alarming rate during this ceremony.
Ceremomal killing of chickens—The invocation to the ancestors
finished, some chickens are usually killed. The ceremonial killing of
chickens is performed by cutting their throats with a sliver of bamboo.
The blood is caught in a vessel and a prayer repeated as the chicken
is dying. The chicken is then held over the fire until its feathers are
burned off, when it is cut up with a knife or by a sawing motion of the
bamboo sliver and put into a pot to boil. The intestines are stripped
of their contents by being drawn between the thumb and finger. They
are then put on a spit, and broiled before the fire. hey are the portion
of the cook. Of some twelve harvest feasts which I attended, the bamboo
sliver was used at two. At others the knife was used. After the chicken
has been killed, the blades of two rwno stalks are tied in a peculiar
manner, and the feet of the chicken stuck into these. Pieces of betel
nuts wrapped in betel leaves and stuck on little sticks are tied in the
blades. The runo stalks, so adorned and called paghing, are placed one
on each side of the gate of the fence surrounding the granaries, or in
the fence in front of the granary door. ‘They are given to the pili,
the spirit that guards the granary against thieves.
The inyocation of the ancestors proceeds in a rather leisurely manner,
and it is generally noon or even later when it is finished. The chickens
that have been killed and cooked are not eaten, but are put in a wide,
flat basket as an offering to the spirits that come to the feast. In fact
the party has not eaten anything since the night of the previous day and
continues to fast until the ceremonies are finished. ;
The Ifugao conception of the universe—In order to make what
follows intelligible, it is necessary to explain the universe according to
the Ifugao’s idea. The Ifugao conceives of three worlds: the Sky World,
the Harth World, and the Under World. Lach is populated by a variety
of spirits, which live in groups of houses, in trees, gullies, springs,
waterfalls, currents, stones, and houses made of skulls. There they
abide much as mortals do. They have an insatiable appetite for pig
meat, betel nuts, and wines; some of them at least need bolos, blankets,
beads, and other things that man uses. In addition to the three worlds
mentioned before, there are two regions, places where the three worlds
meet: The Hast, Lagod, and the West, Daya. In the Hast live some
very vicious place-spirits. The spirits in the Hast are much more num-
erous than those in the West. The Kiangan Ifugaos say that they
themselves came from the Hast, which probably accounts for the fact
that the Hast is more thickly populated with spirits. There is no north-
ern nor southern region thus populated.” In fact, there are no words
- 47 Villaverde is in error when he states that Kadungayan, the place where souls
of those who die a natural death live, is to the north. This Journal, Sec. A
(1909), 4, 248. Kadungayan is in the East.
HARVEST FEAST OF THE KIANGAN IFUGAO. 89
in the language for north and south. If a Kiangan man wishes to say
north, he names some remote place toward the north, as ud Banawul,
toward Banaue, a village in a northerly direction from Kiangan.
Invocation of the makalun. Monmakalun.—The makalun,* the spir-
its that make men forget, that remind or suggest to them, are next
invoked. The makalun may work a man great injury by causing him
to forget the debts that are owed him, to lose spear or bolo, and so on.
“The makalun are like police, also,” say the Ifugaos, “they bring other
spirits to the feast.” This simile is perfectly clear when it is under-
stood that a very small part of the work of an Ifugao policeman consists
in preserving the peace, and that by far the greater part of his work
consists in calling cabecillas ** and kadargyan for consultation ; in carry-
ing instructions to foremen on the trails; carrying the mails and the
like. The makalun are messengers of the other spirits and of those
men who know how to call on them in the right way. As it was ex-
plained to me, the makalun, when sent to call spirits to a feast, notify
the chief spirit in each of the various villages of spirits. This chief
spirit notifies the others that such and such an Ifugao is making a
harvest feast, and that such and such spirits may go to it. An old man
told me that the makalun tells the chief or cabecilla of the spirits some-
thing like this:
The men are harvesting. Let us go to the granary of Kadamon and Gagaya.
We will drink rice wine. They will give us their pigs, chickens, and rice. We
will chew betel nuts.”
Some of the makalun most frequently invoked are: Ud Lagod (in
the Hast) Tayaban,** nak Balud;?? Tayaban, nak Tagudan; Taya-
ban, nak Manguli. Ud Kabunian (in the Sky World) Tayaban, nak
Dalogdogan; Tayaban, nak Balitian; Tayaban, nak Amkidul; Bugan,
nak Numbian; Bugan, nak Balitian; Bugan, nak Abugai. Ud Dalom
(in the Under World) Tayaban, nak Ginita; Tayaban, nak Bahinag;
Tayaban, nak Litnak. The number of makalun and the list of spirits
that may be called upon to serve as makalun, varies considerably at
different feasts. This is the most variable, and in fact the only greatly
variable, feature of the harvest feast as performed in Kiangan villages.
% Makalun: ma, able; kal, word, speech; makalun, one who is able to tell or
-to summon.
Spanish word used in the Philippines in the sense of chief.
a0 Mon-ani di Ipuwao. Ume-tako hi kalumaga di Kondamon ya
Are agents of harvesting the human beings. Will-go-we the granary of Kodamon an
Gagaya; Manginum-tako baya. Idat-tako babui, ya manok ya page-da.
Gagaya; ~-Will-be-agents-of-drinking-wine. Will give us the pig, the chickens, the rice-their.
Monmomma-tako.
Wiill-be-agents-of-chewing-betel-we.
“Tayaban. See under heading “The Tayabans” of this article.
2 Nak, son of.
90 BARTON.
The people call the makalun thus, drinking quantities of rice wine at
the same time:
Come thou, Tayaban, the Messenger Deity, son of * * *. Notify the souls
of our ancestors to come. Notify the Deities of the Sky World, of the Under
World, of the East, of the West, to come. Notify our relatives and our compan-
ions. Summon Banuyuk of Panuyu. In order to speed the harvesters of the
rice; in order to multiply the bundles of the rice. There are rice wine and betel
nuts and betel leaves here.”
These and similar phrases are repeated over and oyer, the fervor of
the feasters growing the while.
Suddenly some of the feasters, perhaps three or four, perhaps a dozen,
are seized upon and possessed by an equal number of makalun. Through
these human agencies, the makalun chant:
We will call your relatives and companions and the spirits of the Under World,
of the Sky World, of the East, and of the West, because you are making a
harvest feast.™
So ends the second ceremony of the feast, the makalun leaving the
bodies of those whom they have possessed and starting off on their errand
immediately.
The earth gods and the sky gods.—These deites, of all those whom the
Ifugao calls to the harvest feast, are the only ones of sufficient dignity
to be termed gods. Their benevolence generally exceeds their malice,
which is not true of the other deities; and they control some of the
forces of nature.2® Bahiwag and his brothers, Dunuan and Tinukud
live in the Under World. They are thought to have a great deal to do
with the growth of plants, especially with germination. Dalogdogan,
Balitian, and Bayuhibis live in the Sky World and control the weather.
Balitian makes rain and Bayuhibis makes mist. They are brothers of
8 Sa-a-a-t Umalika Tayaban an Makalun, nak * * *. Kalunuwm di linavaca
di amud ta umalida. Kalunum di bagol ud Kabunian, ud Dalom, ud Lagod, ud
Daya, ta umalida. Kalunum di mundomang® ya nunhalug. Pananduan hi Ba-
nuyuk ud Panuyu. Ta ikuadin di monagamid di page; ta gumalutigid di udung »
di page. Tehtu baya ya momma ya hapid.
24 Sa-a-a-t Komalum-kami mundomang,° manhalung Idalom®
Say! Will-be-agents-of-calling-we relatives companions Residents-of-the
Under-World
Tkabunian Mlagod Ipaddan® te mon-kolating-kayo.
Residents-of-the Sky-World Residents-of-the Residents of the West because agents-of-perform-
East. ing-harvest-feast-you.
a Mundomang: relatives, including relatives by blood and relatives by marriage.
b Udung, butt of the manojo of rice; poetically, the whole manojo. i
© Mundomang: See note a.
a7, as a prefix in the Kiangan dialect, denotes residents of; as, for example, Ikiangan,
residents of Kiangan ; Jdalom, residents of Dalom, the Under World.
e Paddan, a place to the west; figurative term for West.
> Another quality of their godhood is that so far as.any Ifugao knows, they
have always existed. They were not born of parents. There is no story of their
creation so far as I have been able to ascertain.
HARVEST FEAST OF THE KIANGAN IFUGAO. 9]
Amkidul and Bagilat, who respectively make thunder and lightning.
These gods are the same throughout Ifugao-land, notwithstanding the
fact that there are ten or twelve different dialects in the subprovince.
They are invoked by the entire body of feasters, in the usual high,
falsetto voice, in these or similar phrases:
Oh come! Bahiwag of the Under World. Drink the rice wine. Take the
pig. Speed the harvesters of rice. Oh! that’s it! Bagol! Make the rice grains
as numerous as the sands. Miraculously increase the rice! Oh! Grant it!
Come thou! Make the rice heads hang over (with weight). Oh! that’s it!*
The gods are called separately and in groups. Suddenly one of the
gods (Bahiwag*" always comes first) comes and possesses a feaster.
The latter springs up, seemingly without premeditation, seizes a dish of
rice wine, or, it may be, one of the big bubud jars, swings it with a
circular motion under the granary, at the same time hopping with the
characteristic Ifugao dance steps. The cries and calls of the feasters
and their white-heat fervor leave no doubt that here is a religion the
letter of which has not yet superseded its spirit. The one possessed
drinks and gives the others to drink, chanting the while:
I come up from below, I, Bahiwag. I behold with favor that you are making
a rice feast. I dance, and I drink the rice wine. Drink, you participants; because
I am giving you to drink. I taste the chicken, the pig, and the rice, as I have
been accustomed to do in times past. Thus I drink in dwelling and granary.
I desire it so year after year.
The one possessed passes to the front of the granary where he executes
a little dance. Another feaster, of either sex, who has been possessed
by Tinukud, one of the other two spirits from the Under World, quickly
follows him, and together they dance and chant:
We are the miraculous increase of the rice. We are the slowness of the rice
to be used up. We are harvest-knives and ties.”
76 Sai! Umali Bahiwag ud Dalom. Angbayam di binadayan. Talim di babut,
Ikwadim di monagamid. Oh-h-h hia! an Bagol! Pumantal di Birgga. Huma-
ngali page. Eh-h-h Dami! Umatlika. Lumatok di bintok. Oh-h-h hia!
7 Bahiwag is chief of the gods of the Lower World. Dalogdogan is chief in
the Sky World. [There seems to be some doubt as to whether these two gods
are considered as leaders in any sense. Eprror.]
8Sa-ai-ai-ai! Limadangakhi Bahiwagud Daul. Belibeliokak Kolatingyo
« Came up I Bahiwag of Below. Object-of- Making-harvest-
sight-mine feast-your
Kadaydowak ya angbayak di binadayan. Tinulpangkayo baliknadan te impirgak
Gift-mine and drink-I the intoxicant. Drink-ye participants because
matoldadawak hi manok ya babuiya page-yo ta impainghak di kakohayan.
give-taste-I the chickensand pigsand rice-your hasbeenhabit-mineinthe time-past.
Mobanum tinulpan i haldon ya kalumaga. Pudhok at hitu katdwotdwon.
Thus (?) drink (in) the dwelling and (inthe) granary like-I so yearly.
°° Tanglé-kami. Gikud-kami. Gipam-kami, binwyu.
92 BARTON.
The second feaster takes the dish of wine from the first and offers it
to him. He bends and drinks a long draught and then returns to his
place on the mat, spewing out the last sup of rice wine on the ground.
(See Pl. III, fig. 1.) The second performer now executes some fancy
steps and chants. He is joined by a third who, after the usual little
dance, relieves his companion of the dish of wine and holds it out at the
level of his waist for the ceremonial drinking. And so it goes until the
drinking has been repeated six times, that is, once for each god.*°
There follows a recess in which the participants relax from the high-
wrought and heated fervor in which they find themselves at the end of this
ceremony. They sing work songs and songs of amusement. At about
this stage of the feast, too, the drunkenness has usually proceeded far
enough for the inevitable boasting about wealth and fields to begin. An
Ifugao’s prestige among his fellows is fixed by the number of rice fields,
of gold neck-ornaments, and agate beads, pamgo, he has, by the number
of feasts he gives, and the number and kind of animals he has killed at
these feasts. These facts determine the trend that the drunken babbling
usually takes. Rare, indeed, are the recesses between ceremonies, from
this pot on, when some particularly poor relative does not amuse the
company with a recital of his enormous wealth and of the feasts he is
going to give.
The anointing. Monlana.—TVhese gods, a lower order of beings than
the preceding, and more to be feared, as they belong to an order more
malicious, now demand attention. Asked if these spirits are bad, the
people say: “Yes, bad; but also good, if treated well.” The people say
that these spirits steal the life of the rice if the customary offerings and
respects are not paid them at harvest time and that they may even
diminish the rice in the granary; but if coaxed and cajoled in the proper
form, they “bring the life of the rice,’ and even increase it during
harvest and after it has been stored in the granary.*t They are invoked
In the feast of Kodamon and Gagaya, the actors were four men and two
women.
1 The old men are very argumentative in their invocations to these and other
malicious spirits. They try to convince them of the error of maliciousness
directed toward those who treat them well. The following is one argument:
“Tf you do evil to those who give you feasts, of what use is it to offer these
feasts? Soon no one will kill pigs for you, or give you betel nuts; because you
prey upon your friends as well as upon those who neglect you.” The following
spirits are usually called on, although the list is slightly varied by additions,
there being a legion of less important spirits of the same class: Lukbukan of
Binuyuk; Alingdayu of Nagadangan,2 Mongahid of Nantogan;@ Binongbong of
Lantogan;2 Humidhid of Tayap;4 Dinkom of Imaloi;a Balud, nak Dinkom of
Nuayan; 2 Tugadan of Ibaya; 4 Intikap of Kahilauan;a Inudoman of * * *.
a Names of places a few miles east or northeast of Kiangan.
HARVEST FEAST OF THE KIANGAN IFUGAO. : 93
by phrases similar to those used in calling the gods in the foregoing
ceremony. A bowl containing chicken grease is passed about by a
feaster, possessed by Tayaban, son of Mongahid, who dances and chants
as he goes. As he passes each head, he dips his finger in the grease
and anoints the head of each person who is taking part. The feasters
shout :
We put oil on our heads, in order to put oil on the heads of the harvesters
of the rice, in order to make the rice increase.**
The people can not explain this custom of anointing, nor the chant
that accompanies it. They only say, “That is the right way to perform
a harvest feast.” The following explanation is favored by certain eyi-
dence, and presented to the reader for what it may be worth. It is to
be noted that all these spirits are place-spirits, and that their residence,
Binuyuk, Nagadaigan, Nantogan, etc., are all places in the Hast, which,
according to the Kiangan Ifugaos, is the cradle of their tribe. Now
when an Ifugao makes a new rice-field, he always performs a ceremonial
feast called Jaityalang, killing some chickens to appease the spirit who
resides m the locality. Otherwise, the place-spirit would make all sick
who disputed dominion with him and disturbed his peace by working
his land. He would cause the field to be washed away, the rats to eat
the young rice-plants; in short, he would make the field an utter failure.
It may be that in times past this ceremony was performed annually,
whenever the land was worked or whenever the crop was harvested; that
the workers marked themselves with fat of the sacrificed chickens in
order that the place-spirit might know those who had made the proper
sacrifice; that the custom still survives in the harvest feast; and that
the feasters, as they say, anoint themselves “in order to put oil on the
heads of the harvesters.” The custom, so explained, has points in com-
mon with the Hebrew Passover. Like the angel of the Lord, these
terrible spirits “pass over” those who present evidence of having complied
with the requirenients.** These faithful ones the spirits do not make
sick nor punish by stealing the life of the rice. If, as the Kiangan Ifugao
says, these spirits come from the Hast, it is to be noted that they still
pay homage to the place-spirits of their former habitat; and,‘hallowed by
time, they now rank little lower than gods.
82 Monbelabela-kami ta monbelabela di monagamid di page,
We-put-oil-on-our-heads in-order-to put-oil-on-the-heads of-the harvesters of the rice
ta gumikud
in-order-to-make-the-rice-increase.
The meaning of white chicken feathers worn in the hair, now purely orna-
mental, at first may have been a demonstration to the spirits that the wearer
had made the proper sacrifice.
94 - ; BARTON.
After the foregoing ceremony, and in preparation for the succeeding
one, an old man anoints the bamboo shakers, saying:
I anoint the palipal in order to do the same to.the rice; to make soft and
tough the rice (straw) in the fields; to speed. the harvesters; to multiply the
bundles of rice in the fields in order that the harvest may be great; in order
that the rice heads may hang down;* so that the harvest will be heavy; in order
that the empty space in the granary may be filled with plenty.®
The tayaban. Monligid. (Procession with shakers.)—The tayaban
are predatory spirits almost without redeeming qualities. They are
able, it is said, to increase the rice, “because they are divinities;” but
this is through analogy with the place-spirits, and the gods of the Sky
and Under Worlds. As a matter of fact, not much is expected of them
except neutrality. If this nuetrality is not secured, they steal “the life
of the rice;” they decrease it after it is stored in the granary; they fly
in the night, hunting linawwa, souls that have wandered off in dreams ;37
they lull the foetuses of pregnant women. Tayaban hi Apolili, is the
genius of landslides. The tayaban that are called to the rice feast are
Tayaban, nak Lukbuban; Oltagon, his sister; Tayaban, nak Alingdayu;
Tayaban, nak Binongbong ; Indagan, his sister; Tayaban, nak Mongahid ;
Tayaban Kawaéngwangan;** Tayaban, nak Humidhid; Tayaban, nak
Tugadan; Tayaban, nak Manguli; Tayaban, hi Duyug;* Tayaban, nak
Dinkom; Tayaban, nak Balud; Tayaban Inudoman.
The tayaban are summoned orally in much the same manner as the
spirits in the two foregoing ceremonies. They are asked to increase
the rice, multiply the grains and bundles and make them heavy, “In
the hope,” said an old man, “that they will hear what the other spirits
do, and do likewise through shame.” When the tayaban come, they take
possession of the feasters, by twos, usually a man and a woman, the man
first. The tayaban then cause them to take palipal,*° bamboo clappers,
So that it will not fall down, and the grain be scattered and lost.
* From weight.
% Tlana-ak hi palipal ta ukulan di page; humayumut ya pomatlag indalungene ;
ta ikwadin di monagamid; ta gumalutigid udung nan indalunrgene hi bananu, ta
dakol ni dnian; lumatuk di bintok ta dakol di dnian, ta inhigup natdangan di
hinumpkal. ~
“They carry away and imprison the linawwa, thus causing the person whose
linawwa was stolen to languish and die. The body without a linawwa is like a
palm tree without a bud.
8 Kawangwangan; of the streams. Wangwang, a stream; ka, a prefix of ab-
straction and denoting extension.
®Tayaban hi Duyug. Tayaban of the baliti tree.
“Mr. H. Otley Beyer, of the division of ethnology, Bureau of Science, tells
me that in Banaue, if a feaster breaks a palipal, he must make an expensive
feast to ward off misfortune, and is tabooed from taking part in any other harvest
feast until the next year. This is probably the case in Kiangan also.
HARVEST FEAST OF THE KIANGAN IFUGAO. 95
and with the characteristic Ifugao ceremonial steps, proceed around the
granary, or if there be, as there usually is, more than one granary in the
inclosure, to proceed around all of them. (See Pl. III, fig. 2.) At
each of the four corners, the palipal is outstretched toward the sky and
sharply clapped. (See Pl. IV, fig. 1.) While this procession is passing
the feasters are fervently calling on the tayaban in high falsetto voices,
and telling them what is desired. They say:
“Do not travel through our houses and our granaries and our villages. Fly
over them. Do not frequent our fields nor our forests nor our roads. Fly
around them. MHarass our enemies. Do not diminish our rice. Increase it.” And
so on.
As the actors complete the circuit, a feaster with a cup of wine in his
hand executes a little dance before the pig and pours on it a little. rice
wine, saying at the same time, “Get the pig, you spirits.”* After the
wine has been poured on, he says: “Oh, that’s it! A lbation has been
made the spirits !’4* This circuit is performed four or six times. Usually
the first actor is relieved by others. At the completion of each circuit,
wine is poured on the pig.
Coming of Buluhan, Monbuluhan.—After a recess Buluhan, nak Luk-
buban of Binuyuk,** is called. Buluhan is conceived of as an enormous
creeping being, like a snake. He is called on in the usual phrases to
come and partake of the feast and to increase the rice. Finally, he comes
and possesses a feaster. The one so possessed takes a piece of betel nut
in his mouth and a betel leaf. With these between his teeth, the leaf
projecting like a snake’s forked tongue, he squirms and wriggles over
the rice that is stacked under the eaves of one side of the granary (for
no rice is put into the granary until after the feast) in imitation of the
creeping of a snake. He chants:
I have come from the Hast, I, Buluhan, son of Lukbuban, who live in Binuyuk.
I give (what you ask). I increase the rice. I drink the rice wine, as I have
been accustomed to in time past.*
The feaster wriggles to a bowl of bwbud, rears his head and gazes at
the pig. At the same time, another feaster pours rice wine on the betel
nut from his mouth and drinks from the dish.
“Talim di baboi dakayun bagol.
“O hia! Nagilig an bagol.
‘““ Binuyuk, a place in the East.
“ Himungduak® hi Buluhan, nak Lukbuban Ibinuyuk,> kadayaowak ta huma-
ngale page. Angbayak di binadayan ta impayinhuk di kakohayan.
® Himungdu, come from the East. Humabang, come from the West. Lumadang, come
from the underworld. Nunudnud, come down from the Sky World. These words are
used only in religious ceremonies.
» Ibinuyuk, residents of Binuyuk.
96 BARTON.
Bugan.—Bugan, nak Pundakugan, is the owner of all the locusts.
“Locusts,” say the Ifugaos, “are her chickens.” A woman takes betel
nuts and betel leaves, with some malt,** bubud, in a wooden bowl, and
dances in front of the granary, one hand upraised. She waves her hand,
saying: “Bugan of Binuyuk, daughter of Pundakugan, betel nuts, betel
leaves.”#°
The feasters invite Bugan with loud cries, and the old men pray to
her and argue with her against the folly of injuring her friends. The
argument may run:
Turn your grasshoppers on the fields of our enemies, or of those who do not
give you the things you want, and do not injure us, your friends, who give you
rice wine, betel nuts, and pig.
As the woman dances, a libation is poured on the pig. Bugan nak
Humanun tells her husband to go at night to steal the life of the rice
of those toward whom she is spiteful. She is invited to the feast by
the same ceremony as that observed in inviting Bugan Pundakugan.
The wind deities. The piok.’—The piok are possessed of consider-
able power over the forces of nature; they control the strong winds, the
winds that come with typhoons; they can increase the rice during harvest
time; they can steal its life away and cause it to languish and die before
maturity. It is a very noteworthy fact that in the religion of the Ifu-
gao there is no clearly defined division of labor between the spirits or
classes of spirits. Thus, the place spirits, the bugan, the puiok, and even
the tayaban, are besought to increase the harvest, although the puwok are
primarily controllers of the strong winds and the tayaban are predatory
spirits. The wind deities usually invoked are four: Dinipaan of
Paadan; ** Piok of Halamban; *® Puok of Ambatu; °° Puok of the Hast.
The distinction between the puiok of Halamban and the piok of Am-
batu is that strong winds caused by the former are not accompanied by
rain, while strong winds caused by the latter are so accompanied.
The feasters invite the piok in the usual terms and call upon them
to increase the rice. The special phrases of the invocation of these
spirits are:
“© The Ifugao not only drink rice wine, but eat its malt.
‘© Bugan ud Binuyuk, nak Pundakugan bibihalag dangaidahan.
“ Piok: a strong wind.
*® Paddan, a place about three miles west of Kiangan.
* Halamban, a place toward the south.
°° Ambatu, a place toward the south.
HARVEST FEAST OF THE KIANGAN IFUGAO. Ti
. Rice wind, wave the rice in the fields, but return its soul (life?). Make
healthy its soul. Do not fell the houses and granaries. Do not summon the
rains because we are harvesting. Here, you have rice wine and pig, ete.”
A feaster is possessed. He takes a basket containing betel nuts and
betel leaves, malt, and a coconut shell containing rice wine, and with
a palipal in hand proceeds swiftly ** about the granary, with the Ifugao
ceremonial steps, rattling the bamboo clapper vigorously ** at the four
corners of the granaries and chanting as he goes:
We are the slowness of rice to be used up. We are the miraculous increase
of the rice. We are the life of the rice. We are the harvest knives.
This procession is repeated four times, once for each puok. At the
termination of each circuit, rice wine is poured on the pig, the person
pouring it crying: “A libation has been made unto all you puok.”**
Usually the circuit is performed by a different actor each time. (See
JPL, WAYS, see)
The bakayauan. Monbakayauan.—The bakayauan are powerful deities
that go armed with spears. They are hunting spirits. Some of them
have dogs. ‘They are offered sacrifices by hunters, and go to the chase
with them. Most of them live in the Sky World, some in the Under
World, and others have special places in the Hast.*°
The feasters begin calling bakayauan to the feast. Suddenly one of
their number springs up, seizes a spear °® from those stuck in the ground
1 Pumptiok hi page, inumyum di page, mu ibangad di linawwa-na. Adikayo
tiwan di halaon ya kalumaga. Adikayo ayagan di udan te monaki-kami. Tehtu
binabudan ya babui, ete. é
** Note the connection in the Ifugao’s mind between the passage of the wind
over the rice and its health and growth.
88 Note that the manner in which this procession is made is symbolic of a
strong wind.
“ Nagilig dakayun piok, amin. i
These deities are: Bakayauan, nak Panuya, Kabunian; Bakayauan, nak
Balitian, Kabunian; Bakayauan hi Tayaban, Kabunian; Bakayauan, nak Hol-
dayan, Kabunian; Bakayauan, nak Mangamalig, Kabunian; Bakayauan, nak
Balitok, Itapugan; Bakayauan, nak Lauan, Dukligan; Bakayauan, nak Dinlugan
ud Dulom; Bakayauan, nak Domagaan, Kabunian; Bakayauan, nak Lakmayan,
Kabunjan; Bakayauan, nak Buluhan, Kabunian; Bakayauan, nak Amgumagub,
Kabunian.
The spear must be a bright handsome one, of the class called bolobog, or
of that termed gayang. This latter is called by Jenks the “anito spear.” At
one feast I witnessed in a small group of houses no handsome spear of either
of these two classes could be found. The procession about the granary was
omitted.
98 BARTON.
near by, dances before the door and then proceeds around the granary.
Holding the weapon in both hands, he brandishes it with an upward
and downward wave-like motion as he goes. His black eyes shine; he
has the appearance and glance of a madman. He chants:
flarass (or, bewitch; torture) the enemies, and the rice disease, and the
sorcerers (those who do evil through their bad ceremonies) and the pests.”
The feasters cry out in the same and similar phrases and with the
ever present prayer that the spirits increase the rice. The procession is
repeated two, four, six, or eight times. At the end of each procession
the actor executes a little dance before the pig, and after two or three
threatening gestures throws the spear across the pig, sticking it in the
ground a meter or so beyond. The spear is thrown from a distance of
three to five meters as near as possible to the pig without injuring him.
At the same time rice wine is poured on the pig, accompanied by the
usual phrases. (See Pl. V, fig. 2.)
The Koliaban, or Coverer.** Monkoliaban.—A blanket dance is the
ceremony of this spirit. (See Pl. VI, fig. 1.) The dancer is believed
to be possessed. The dance is very graceful, and resembles one I have
seen performed by Bagnen and Besao Igorots in Lepanto. The people
invite and beseech the koliaban in the usual terms and in addition make
the following plea:
Cover up (smother) thou the lack of rice, the hungry time, the rice disease,”
and the pest; but do not cover up the chickens, the pigs, and the rice. Cover
up thou the sorcerers, the persons who do evil through bad feasts, and the persons
who cause pests.”
Ceremonial killing of the pig. Monwiwik.—The pole is removed from
between the legs of the pig, which is then turned with its head to the
east, for pigs are usually ceremonially killed facing the east. One man
holds the legs so that the animal can not struggle; the person who is
acting as cook cuts through the skin just below the sternum and pushes
into the chest of the helpless animal a rwno stalk, wiwik, about a foot
7 Hango hangonmo hai binuhul utyai hiba utyai mangidat utyai balandag.
This is probably only a fragment of what he chants. It is all I have obtained
as yet.
Cf. the Sa-rukub rang buni of the Malays. The World Coverer, Malay Magic.
p. 94.
*° The disease of the rice, not the sickness caused by the new rice as described
by Jenks. The Bontok Igorot, Ethnological Survey Publications. Manila (1905)
1, 107.
% Koliaban-mo hai bitel, hai duian, hai hiba ya hai balangdan; mu adim ko- -
liaban hai manok utyai babui utyai page. Koliabanmo hai maigidut, hai manong-
dong, utyai mondayapat.
HARVEST FEAST OF THE KIANGAN IFUGAO. 99
long. This he thrusts into the animal’s lungs, the while it squeals
piteously. Generally it takes some time to kill the poor animal, as the
stick is usually too blunt to puncture the walls of the heart or other large
blood vessel, and the animal dies from hemorrhage into the lungs. (See
Pl. VI, fig. 2.) While the pig is being killed the old men pray most
fervently.
Burning the hair off the pig. Monlagim.—The hole in the pig’s breast
is plugged with a piece of runo and the animal is held in the fire, or laid
in the fire until the hair and epidermis are charred. he body is then
scraped. Needless to say, the animal is much bloated by the heat. (See
TEA WADE ait 1)
The Lepanto Igorots go through the same procedure with the pigs
and dogs that they kill.
Dispatching the spirit of the pig. Monhu-aa.—After the pig has been
scraped, a wreath is made of the stick of rwno with which it was killed,
two or three heads of rice, and a spray of hagaga grass. (See Pl. VII,
fig. 2.) The pig is placed in the center of the mat, and decorated with
the wreath. The feasters gather about, and, grave and silent, sit down
while an old priest charges the pig’s soul as follows:
Thou art enwreathed, pig, because thou art a young pig that wast used at a
harvest feast; (and) in order that ye all, rice, hagaga, death stick (wiwik, the
stick used to kill the pig) and pig, may go in company. Rise ye all unto the
Sky World. Arrive unto the quarters of Ampéal, Balitian, Humamu, Wigan,
Bayuhibis, Dulayan, Humok, Dakwigan, Numbian, Baluog, Amgalingan, Banga-
nan, Intoldaon, Umbumabaka. Tell them, pig, that the men killed thee; that
they sacrificed thee. Say thou, pig, “I was sacrificed at a harvest feast.’ Tell
the bagol to increase the rice, to make the rice heavy, in order that the empty
space in the granary may be filled with plenty. Do not remain speechless. Do
not tarry, sleeping, pig.
Thou art enwreathed, pig, because thou art a young pig that wast used at
a harvest feast; (and) in order that ye all, rice, hagaga, death stick and pig
may go in company. Descend ye all unto the Lower World. Arrive unto the
quarters of Bahiwag, Tinukud, Dunuan, Kaliog, Lutwag, Ginita, Humamu. Tell
them, pig, that the men killed thee, that they sacrificed thee. Say thou, pig:
“T was sacrificed at a harvest feast.” Tell the bagol to make the rice heavy
in order that the empty space in the granary may be filled with plenty. Do not
remain speechless. Do not tarry, sleeping, pig.
Thou art enwreathed, pig, because thou art a young pig that wast used at
a harvest feast; (and) in order that ye all, rice, hagaga, death stick, and pig,
may go in company. Proceed ye unto the East. Arrive unto the quarters of
Lukbuban, Binongbong, Alingdayu, Mongahid, Balud, Tugadan, Mangali, Panik-
dapan, Piok, Nabalud, Dinumpitan, Binudbud. Tell them, pig, that the men
killed thee, -ete.
Thou art enwreathed, pig, because thou art a young pig that wast used at a
harvest feast; (and) im order that ye all, rice, hagaga, death stick, and pig,
may go in company. Proceed ye unto Paaidan (the West). Arrive unto the
100 BARTON.
quarters of Kabigat, Dinipaan, Dumugung, Nalipang, Ambatugan. Tell them,
pig, that the men killed thee, ete.”
The cutting up of the pig—The small boys, who have listened patiently
during this rather lengthy prayer, now have their reward. While the
greater part of the animal is eaten at the granary by the feasters and
* Wagéhan daka babui te kinlum daka, te impanga daka page, ta monkakuyug-
kayon page, hagaga, wiwik, ya babui. Tumalakdang-kayo kabunian. Dutnangyo
hudok nan Ampial, hi Balitian, hi Humamu, hi Wigan, hi Bayuhibis, hi Dulayan,
hi Humok, hi Dakwigan, hi Numbian, hi Baluog, hi Amgalingan, hi Banganan,
hi Intoldaon, hi Umbuma-baka. Imbagadaka babui dimatayanda he’a; nangi-
padtianda babui ke he’a. Humapitka babui ‘Impaduyu-ak hi kolating.” Komali
din bagol ta gumikud di page, ta humangale page, ta ihigup natdangan di hi-
numpkal. Adika mahduman. Ugikabo maginaginluk babui.
Wagahan daka babui te kinlum daka, te impangadaka page ta monkakuyug-
kayo page, hagaga, wiwik ya babui. Monudnud-kayo ud Dalom. Dulnangyo
Bahiwag, hi Tinukud, hi Dumnan, hi Lutnak, hi Kaliog, hi Ginitu, hi Humamu.
Imbagadaka babui dimatayanda he’a, nangipadtianda, babui, ke he’a. Humapitka,
babui ‘Impaduyu-ak hi kolating.’ Komali din bagol ta gumikud di page, ta
humangale page ta ihigup di natdangan di hinumpkal. Adika mahduman. Ugi-
kabo maginaginluk, babui.
Wagahan daka babui ta kinlum daka, te impangadaka page, ta monkakuyug-
kayo page, hagaga, wi-wik ya babui. Monuhaal ud Lagod. Dutnangyo Lukbuban,
hi Binongbong, Alingdayu, Mongahid, Balud, Tugadan, Mamngali, Panikdapan,
Pitiok, Nabalud, Dinumpitan, Binudbud. Imbagadaka babui, di matayanda ke
he’a, ete.
Wagahan daka babui te kinlum daka, te impangadaka page, ta monkakuyug-
kayo page, hagaga, wi-wik ya babui. Monuhaal ud Paaidan. Dutnangyo Kabigat,
hi Dinipéan, hi Dumugung, hi Nalipang, hi Ambatugan. Imbagadaka babui
dimatayanda ke he’a, etc.
The following is the first section of the above invocation:
Wagahan dakan babui te kinlum daka te
Object-of-being-decorated-with-wreath- thou pig because young-pig thou because
made-of-hagaga-grass,-stick- Wwith-
which-killed,-and-rice-heads
impangadaka page ta monkakuyug-kayo page hagaga
object sacrificed thou (to) rice in-order-that agent-of-going-in-a-company-ye, rice, hagaga-
grass
wi-wik yababui. Tumalakdang-kayo Kabunian. Dutnangyo
stick-with-which-killed, andpig. Agents-ofrising-ye (unto) Sky-world Objective-of-arrival-
your
hudok nan Ampial, Imbagadaka, babui, dimatayanda
quartersofAmpual, Balitian, etc. (asabove) Object-of-telling-thine, pig, sacle hen
hea; nangipaduanda babui ke hea hwmapitka babui cp pecn eR EGE
thee, agents-of-sacrificing-they, pig of thee: Agents-of-saying. thou, pig, ‘“‘Was-object-of-
sacrifice-
hi kolating’’ Komali din bagol ta gumikud di page,
at the harvest-feast’’ Agent-oftelling the spirits that agents-of-increasing therice,
ta y humangali di page ta thigup
that agents-of-increasing-miraculously therice, in-order-that object-of-being-brought (to)
natdangan di hinumpkal. Adika mahduman. Ugikabo
place-for-ripe-grain (of the granary) the plenty. Do-not-thou-be mute. Do-not- Show either
maginaginilvk, babu.
(emphatic) be-sleepy, pig.
HARVEST FEAST OF THE KIANGAN IFUGAO. 101
harvesters, some of it is distributed to be carried home or cooked at will.
Hach of the priests gets a good piece. A most striking feature is the
lack of variation in the process of cutting up and distributing the pig.
The feet are first cut off. The children eagerly contend for these, and
only the presence of the elders prevents them from coming to blows.
Then the skin and fascia over the belly are cut off, the belly is opened
and the entrails are taken out. The gall bladder is inspected for an
omen. If it is full and dark—as it nearly always is, for the pig has not
eaten for some eighteen to twenty hours—all is well."* The chest of
the pig then is opened and the blood poured out. Some of the clotted
blood is often snatched and eaten by the feasters, for they have fasted
since night of the previous day. The triangular fascia under the lower
jaw is cut off, the head severed from the body, and the body cut into
sufficiently small pieces to go into pots.
The following is the apportionment of the parts of the pig: The head
goes to the owner, for when the flesh has been eaten, the skull will be
hung up outside the granary; the feet, pancreas, genitals, bladder, and
a portion of the liver, to supply the children not already supplied with
some part of the animal; the tail ** to a child or to a man or woman
who may desire it; the skin and fascia of the belly, the skin and the
fascia under the lower jaw, the heart, and the lungs, to the cook, as pay
for his services; the intestines, a highly prized portion, go to the youths
who carry the rice to the granary; the remainder is divided among the
harvesters and feasters.
I have never seen this allotment varied except in one case. In that
instance, the cook, in cutting off the abdominal fascia, which rightfully
fell to his lot, cut off some short ribs with it. The bystanders protested
that the cook was taking more than his just portion and that he was, in
fact, a pig himself.
Continence and the fast during harvest time.—While it usually takes
only one or two days for a family, with the aid of relatives, neighbors,
and the people who come down from the higher villages, to cut their rice,
it is generally five weeks or more from the time the first family begins
harvesting until the last one in the village has finished. During this
% After the examination, the gall bladder is twisted on a stick, and fixed under
the floor of the granary. If by any chance it were empty and dark, it would be
necessary to kill another pig.
The tip of the tail, if it be white, is worn by a girl or woman in the hair
as an ornament; and by a man at the end of the strings by which the neck
ornaments are tied on. See the tips so worn by the dancers in the picture of the
blanket dance. Plate VI, fig. 1.
101776——4
102 BARTON.
time, continence is the rule for the following classes: Persons of im-
portance, those who have a goodly number of rice fields; persons who take
part in the harvest feasts, monbaki; and those who stack the rice in the
granaries, called mangikapia.** The reason given for this practice is that
the bagol do not, at this season, approve of earthly pleasures and joys,
and punish those who indulge in them not only by not increasing, but by
actually decreasing their rice supply. J am informed that continence is
strictly adhered to; and I believe that it is so, knowing, as I do, the
implicit faith of the people in the tenets of their religion. And, besides
this implicit faith, there is the consideration that the members of the
three classes mentioned are middle-aged or elderly persons.°°
During harvest time no Ifugao may eat of the carabao, ox,®® deer,
grasshopper, goat, fish, or snails. It is not forbidden to eat the flesh
of the pig, chicken, or duck. Vegetables, except camotes, may not be
eaten.
This renouncing present pleasures or advantages with the intention of
gaining greater advantages of another kind is an old story in religions
the world over. Self-denial is pleasing to the divinities; too much
prosperity arouses the jealousy of the gods. Who are these mere men
that they should have so much happiness? Let them pay for it!
It is very interesting to find in another Igorot tribe, living under
very different conditions, an observance of celibacy and fast, from re-
markably similar motives. The Igorots of Suyoe, in the Subprovince
of Lepanto, live almost entirely upon the proceeds of their mining, the
climate of their village not permitting the cultivation of rice. I am
informed ®* that when a Suyoc man strikes, or knows that he is about
This office is always performed by elderly men.
® The Eskimo have a similar practice during the whaling season. Says Elie
Reclus: “During the hunting season, the Aleutians often turned their wives out
of doors, forbidding them to cross the threshold of the great kachim.” * * *
Primitive Folk, p. 58.
“Master whale is also a stickler for morality and virtue; he avoids latitudes
frequented by base and dissolute tribes; does not approve of the whalers who
have the honor of attacking him compromising themselves with women during
the whaling season; he would even punish them by some terrible chastisement
if their wives were unfaithful to the conjugal vow during their absence; he
would cause them to perish by a cruel death if their sisters failed in chastity
before marriage.” Ibid, p. 55.
°° In Mayaoyao village the ox is regarded as unclean, and the use of its flesh
as food is interdicted altogether by custom. For this information I am indebted
to Lieutenant-Governor Jeff D. Gallman.
*T am indebted for this information to Major C. E. Nathorst, Philippines
Constabulary, and to Mr. Henry Reeder.
HARVEST FEAST OF THE KIANGAN IFUGAO. 103
to strike, a vein of gold-bearing rock, he quits work, goes home, and
offers to his gods a feast lasting two or three days. From the time tha’
he returns to work until the vein or pocket is exhausted, he drinks no
rice wine, and eats no flesh nor vegetables. He also remains continent.
The reason he gives for this practice is that, otherwise, the spirits
would get angry, and would cause the gold-bearing rock to diminish
rapidly, and soon to fail altogether. Note the parallelism of the customs
and the motives thereof, although the Suyoe man is working his “find”
of ore, and the Kiangan man is cutting his rice crop.
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Bureau of Science No.3 ____----- | 7 | 13 7 4) d6+] 47+
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If bya + in his account of the number of caudal vertebre present
Flower meant that certain terminal caudals were missing, no such meaning
is here intended to be conveyed. In the above table a ++ does not mean
SKELETON IN THE FLYING LEMURS. 155
that the skeleton with respect to the number of caudal vertebre is
imperfect in any of the specimens examined, but that the skeleton of the
tail is finished off distally by an apparently rudimentary vertebra which
lacks the posterior moiety. The truth of this has been confirmed in my
specimens by the use of the microscope. For example, caudal vertebrae
11 to 15 in specimen number 2, very much resemble, upon a casual glance,
some of the joints of the manus or pes, with a shaft and articular extrem-
ities. Now the minute terminal vertebra of the tail in specimen number
2 (and in others) if compared with a phalangeal joint, appears to have
been broken in two at the middle of the shaft, or at a point that in reality
is the middle of the centrum of the vertebra. The + stands for this
“nib” or rudimentary terminal caudal vertebra in my specimens, apd
as such is entitled to recognition in the total count. (See figure 17,
plate V.)
‘From an examination then of six individuals, three of Flower and
three here, it may be stated with certainty that the number of vertebrz
in the spinal column of Cynocephalus, irrespective of species, is markedly
variable, after we pass the 7 cervicals, which are invariably present in all
specimens. There may be 13 or 14 thoracie vertebree (bearing ribs) ;
from 5 to 9 lumber vertebre; from 3 to 5 sacrals, or those that fuse
together to form the “sacrum ;” and, finally, from 14 to 19 caudals, which
in most cases possess in addition (a +) a rudimentary one at the termi-
nation of the tail series.
Throughout the class Mammalia, even including man, the number of
caudal yertebre present in any particular species is subject to considerable
variation. This becomes less and less the case as we pass from the tail to
the cervical division of the spine, where with but very few exceptions 7
is the rule. Manatus among the Sirenia has but 6 cervical vertebrae ;
which is also the case with Cholepus among the Edentates, while in the
same group (Hdentata) Bradypus possesses 9. At the present writing
no other exception to this rule is known to me in the class.
The count may be made to vary, too, by the number we elect to repre-
sent the pelvic sacrum. In Cynocephalus as in other mammals, man
included, the number varies also with the number that fuse together to
form the sacrum. Where they have thus codssified, the bones so united
have been here considered as sacral vertebre; 3 in two instances; 4 in
another. In man they vary from 4 to 6.
All these facts led Flower ** to state that—
It must never be forgotten that although the division of the vertebral column
into distinct regions is convenient for descriptive purposes, at the contiguous
extremities of the regions the characters of the vertebre of one region are apt
to blend into those of the next, either normally or as peculiarities of individual
skeletons.
* Osteology of the Mammalia, 78.
156 _ SHUFELDT.
In describing the spinal column in any mammal it has been the rule
of the present writer to consider all those vertebree between the skull and
the first one in the chain, proceeding backward, that bears a pair of true,
free ribs, as cervical vertebrz; all those bearing a pair of true, free ribs,
as dorsal or thoracic vertebre ; all those between these last and where they
codssify to form the “pelvic sacrum,” as lumbar vertebre; all those fusing
together between the ilia of the pelvis, as sacral vertebre; and all the
rest to the end of the column, or chain, as caudal vertebre. This rule
has been here applied to Cynocephalus. (Figures of vertebre will be
found upon Plates II to V of the present memoir, that is figures 7, 8, 10,
11, 12, 13, 14, and 17.)
« In describing the spinal column of the insectivore here being considered,
the’ specimen furnished by Steere has been selected; constant references,
however, will be made to the others, designating them as 2 and 3, respec-
tively, as already indicated.
There is nothing especially unusual in the vertebral column of Cyno-
cephalus, as it is strictly mammalian in character, with all of the vertebra
‘reduced to their simplest forms for an imsectivorous animal. Hven in
the matter of number these bones may agree with others among the
Insectivora, as in the case of the common Huropean mole (Talpa europea),
which has in its vertebral column 7 cervical, 13 thoracic, 6 lumbar, 5
sacral, and 11 caudal vertebra, the tail simply being somewhat longer in
Cynocephalus. :
Viewed in its entirety in the latter it is to be noted that the atlas is
by far the largest vertebra in the chain; the axis is the next in size and
is considerably smaller, being about equal in bulk to the last lumbar.
The succeeding five cervical, and the first dorsal are all large vertebre.
which very gradually decrease in size as we approach the dorsal region of
the spine. From the second dorsal to the seventh inclusive the vertebre
continue gradually to diminish in size; except the terminal caudals, the
seventh dorsal is about the smallest one in the column; beyond the seventh
dorsal the vertebre gradually increase again, become much larger and of
different character in the lumbar region, and terminate with the largest
one of all, which articulates with the anterior vertebra of the pelvic sacrum.
The first lumbar bears considerable resemblance to the last dorsal, but is
distinguished by not supporting a pair of facets for ribs.
The vertebre composing the sacrum fuse very solidly, but the lines
of demarcation between the central and the neural spines are always more
or less distinguishable, more so in some specimens (1 and 3) than in
others (2). The first caudal vertebra, which is free, resembles the last
sacral, and the same may be said of the second, third, and fourth caudals,
although the resemblance becomes gradually less evident as we proceed
toward the end of the tail. This dissimilarity continues to increase rather
rapidly, although never abruptly, as we follow the caudal series to its
SKELETON IN THE FLYING LEMURS. 157
termination, each succeeding vertebra having its various apophyses disap-
pear, becoming lengthened and much simpler in character, straight and
subeylindrical, and with interarticulations of the most primitive kind.
As we come to the last four or five caudals they gradually shorten again,
being in this region represented by mere delicate straight rods, with
slightly enlarged articular ends, and finally terminate in a minute osseous
tip, the smallest vertebra in the entire series, hardly worthy of the name
(figure 17).
No neural spine occurs upon the atlas vertebra, although a very prom-
inent one, arising from the entire length of the neural arch is to be
found upon the axis. Its superior border is convex from before, backward.
The neural spine in the remaining five cervicals is very markedly reduced
in size, in each bone being represented by a mere stumpy process. In the
first dorsal it starts to imerease again, being situated posteriorly and
directed backward. It then gradually increases in size; becomes nearly
vertical, quadrilateral in outline, and almost imperceptibly dwarfs once
more to include the eighth dorsal, when again its proportions increase, and
this continues as we pass through the lumbar region. In the mid-series
of the vertebre in this latter locality in the Steere specimen, the neural
spine is a very conspicuous feature of the bone, being lofty, quadrilateral
in outline, and with a thickened superior border; it extends the entire
length of the neural arch, being about one-half the size on the last lumbar
vertebra. In other individuals these neural spines are not nearly so con-
spicuous (figure 17) as the ones just described (figure 7, Plate I1).
Neural spines are always present upon the sacrum, but here by fusion
they constitute a single plate of bone, being individualized only by the
thickened superior borders (figure 8). This plate is not so high poste-
riorly as it is in front, while at the same time it extends the entire length
of the sacral neural arch.
On the leading caudal vertebra we find a fairly well-developed neural
spine of about the same size as the one on the last dorsal vertebra. It is
centrally situated. This is the case with the next two succeeding caudals,
but in these the neural spine is becoming aborted, while in the fourth
caudal it may be only just evident, to entirely disappear in the vertebra
next following, and not be produced again for the balance of the vertebral
elements in the skeleton of the caudal appendage.
. A mere mesial raised line represents the hemal process or hemapo-
physis, in the axis and the third cervical vertebra; for the rest of the
column no such structure is present, while the caudal vertebrae appear to
be entirely lacking in chevron bones. These last are found in many
mammals, as, for example, among marsupials, the Edentata, Cetacez.
many rodents, carnivores, and even in some Insectivora, as Rhynchocyon,
where, according to Flower, they “are well developed and bifid.” *°
* Osteology of the Mammalia (1885), 73.
158 SHUFELDT.
Returning to the atlas (figure 10) we find, in addition to characters
already ascribed to it, that it possesses upon its anterior aspect the usual
two, extensive, cup-shaped facets intended for the condyles at the back
of the cranium. They face forward and inward in about equal propor-
tions, and are completely out of view when the vertebra is regarded from
directly above. ‘The neural canal is short and cylindrical, being covered
by the broad neural arch above, but very slightly so protected ventrally.
Each apophysial, transverse, lateral expansion is twice pierced by for-
amina; the anterior ones are for the vertebral arteries and suboccipital
nerves, the other pair, entering the neural canal at its sides, are for the
vertebral arteries. On the posterior floor of the neural canal, the articular
surface for the odontoid process of the axis and the entire fore part of the
latter bone, save its neural spine, are continuous, thus affording very
considerable play between the two bones. The under sides of the nearly
horizontal, lateral, apophysial plates of the atlas are decidedly concave,
with the mesial, almost entirely aborted, hypophysial tubercle standing
between them behind.
This ventral surface of the atlas is bounded in front. by a deep concave
articular border with the concavity directed backward. A similar border
with thickened edge forms the posterior boundary; its concavity, which
is not so profound, is directed forward. Between the nearest points of
these two concaye borders in the middle line, the separating isthmus of
bone measures only a few millimeters. The margins of the lateral edges
of this vertebra are sharp and convex outward.
Passing next to the axis, or second cervical vertebra, it is to be noted
that its odontoid process is but fairly well produced, being bluntly trian-
gular in form, considerably compressed from above, downward, and to-
gether with the rest of the articular surface on that aspect of the bone,
projecting entirely beyond the neural spine above it. This is by no means
always the case in mammals, for among certain Felide and Canide it
may be observed that the anterior projection of the neural spine in this
vertebra overhangs the odontoid process. There are no prezygapophyses,
while the postzygapophyses are much aborted, the elliptical articular
facets, which they support in other vertebre being represented, one on
either side, by similar surfaces situated beneath the neural laminz. They
project beyond the small and vertically much compressed centrum, which
presents, posteriorly, a rather large facet for the third vertebra. (Plate
III, figure 11.) The transverse processes are moderate in size, triangular
in outline, and much compressed in the vertical direction. No foramen
for the passage of the vertebral artery, on either side, is to be found in
the axis, while the cylindrical neural canal is much smaller than it is in
the atlas. In fact it has about the same caliber and form throughout
the cervical series as it has in the axis now being considered.
The remaining five cervicals are all very much alike, and we find each
SKELETON IN THE FLYING LEMURS. 159
of them perforated upon either side, in the longitudinal direction, by the
foramen for the vertebral-artery. Im each the centrum is much» com-
pressed from above, downward, which results in giving the articular facet
at either end a transverse elliptical form, the concave one being behind,
the convex one in front. The prezygapophyses are quite individualized
and project directly forward beyond the centra and the neural arch.
Postzygapophyses practically agree with what has been described for the
axis. All these vertebrae have a broad, compressed appearance with
their flat ventral aspects quadrilateral in outline. Small and stumpy in
the third cervical, the transverse processes become gradually more con-
spicuous to include the seventh, or last cervical, where they are produced
both forward and backward from a broad common pedicle.
Among the leading dorsal vertebre the centra are much compressed
as we found them in the cervicals, but they gradually become more
cylindrical in form to the close of the series. Reniform in outline, the
articular facets at either end have their concave edges upward.
Greatly reduced in size and caliber throughout the dorsal region, the
neural canal is slightly compressed from above, downward, in the first
few dorsals, finally to become cylindrical among the ultimate ones. This
continues to be the case through the lumbar vertebre, until we arrive
at the last lumbar, where the canal is very much compressed from above,
downward, and with this form passes through the sacrum and the first
four caudal yertebre. On the fourth caudal the spinal cord receives its
last and very scant osseous protection, passing through a delicate little
arch on the superior aspect of the bone, posteriorly.
Among all the dorsal vertebrae the diapophyses, or transverse processes,
are short and thick, and in all cases project directly outward from their
bases. At their nether extremities we note the usual facets for the
tubercles of the ribs articulated with them at these points. The capitular
facets for the heads of the ribs are shared in each case throughout the
dorsal series by two vertebrx, by which is meant that one-half of the facet
(a demifacet) is on the centrum of one vertebra and the other half on the
side of the centrum of the vertebra next following it. No exception to
this rule has been met with in the three specimens examined. ZAyga-
pophysial processes here present their usual mammalian characters, the
postzygapophyses only becoming differentiated as true processes in the
last few bones of this region.
The intervertebral foramina for the entire spinal column are formed
about as they are throughout the mammalian series, including man.
They are large in the cervical region, very much smaller in the dorsal
section, and increase in size again in the lumbar where they are longitu-
dinally slit-like, and are found in each ‘case between the centrum and the
long, backwardly directed, spiny anapophysis on either side, at the pos-
terior end of the vertebra (figure 7).
102305——3
160 oars! SHUFELDT.
These anapophysial processes of the lumbar vertebre, where present,
are quite characteristic. Hach one on either side forms a deep notch
with the postzygapophysis next to it on the same vertebra. Into this
notch, when the bones of the spine are normally articulated, fits the
prezygapophysis (of that side) of the next succeeding vertebra, the com-.
bination making a very close interlocking articulation, which, when taken
altogether for the six leading lumbars, accounts for the remarkable fixity
and stability of this part of the column in Cynocephalus. In the last
two lumbar vertebree these anapophysial processes are entirely aborted,
as are the transverse processes in the first two lumbars. After that,
however, these diapophyses begin to appear again, being represented by
thin, quadrilateral, horizontal plates of bone of good proportions. They
are thick and strong in the last lumbar, and claw-shaped in the three that
precede it with the apices of the claws directed to the front. (Plate IV,
figure 13.) Metapophyses of a very rudimentary type are also to be seen
in the mid-lumbar vertebre ; in any case the most of the projection belongs
in reality to the anterior zygapophysis, an exception being found in the
last lumbar vertebra, where these processes are much better defined and
rather more prominent.
In Steere’s specimen the sacrum is a very it bone, composed of three
vertebre thoroughly fused together. The leading one has double the bulk
of the last, while the middle one is massive anteriorly and slopes away
behind (Plate IV, figure 14). Anteriorly, the first sacral presents the
usual facets, processes, and surfaces to articulate with those on the hinder
aspect of the last lumbar. So, too, the posterior face of the third sacral
is similarly modified in order to meet the requirements of an articulation
with the anterior face of the first caudal vertebra. laterally, the entire
mass of the first sacral and the anterior moiety of the second, are enlarged,
thickened, and curved ventrad to support on their outer aspect a large,
subelliptical, articular surface for the ilium of the same side. This
surface looks upward and outward, and the major axis of the ellipse is
in line with the longitudinal axis of the spinal column, being parallel to
the long axis of the ilium when the bones are normally articulated. There
are two pairs of foramina on the ventral surface of the sacrum for the
exit of the anterior roots of the spinal nerves. Similar pairs of foramina,
for the posterior roots, occur on the dorsal aspect of the bone directly
opposite these; then the foramina for the pairs of roots of the spinal
nerves both anterior and posterior to these are only completed when the
last lumbar and first caudal vertebra are in position and duly articulated
in the column, being represented only by shallow notches in front and
behind when we study the sacrum as a single bone.
Considerable compression in the vertical direction is noticed in the
first four caudal vertebra. The fifth is rather stocky, after which they
commence to elongate and lose their apophyses and the other usual
SKELETON IN THE FLYING LEMURS. 161
vertebral characters of the bones in the fore part of the column. The
lateral processes, especially, are developed in the first four caudals, most
so in the third and fourth, where they are extensive horizontal plates with
circular limiting borders. Zygapophysial processes are well developed in
the leading caudals, particularly the prezygapophyses, which subsequently,
as we pass down the skeleton of the tail, become a pair of rounded tubercles
situated side by side on the supero-anterior aspect of the bone, » These
persist in a number of vertebra as we pass toward the end of the tail.
On the ventral aspect of the skeleton of this part of the vertebral chain
in Steere’s specimen, between. the sixth and seventh and the seventh and
eighth vertebr, and situated directly over the intervertebral articulations,
we note a pair of minute ossicles, ellipsoidal in form, and placed side
by side, at an interval of about one millimeter. They are perfectly free
and are held in place by delicate ligaments. Possibly similar pairs may
be found posteriorly between a few more vertebra, but after that they
surely disappear altogether. These last have evidently been lost in the
specimen, and it is fair to presume that these ossicles probably represent
rudimentary chevron bones.
Flower,!’ under the Insectivora, makes no mention of the ribs and
sternum, although he lightly touches upon them for Talpa, Sorex, Hrina-
ceus, and Rhynchocyon.
Viewed as a whole the osseus framework of the thorax in Cynocephalus
is quite in keeping with what we meet with in this part of the skeleton
in any average mammal, being decidedly more so than in T'alpa, although
the mole and the colugo each possess 13 pairs of ribs.
The chest capacity of Cynocephalus is considerable, notwithstanding
the fact that it is much contracted anteriorly, where it is bounded by the
first pair of ribs, the first dorsal vertebra, and the presternum. From
this region it gradually, though very uniformly, expands to the plane of
its posterior termination, where it has an average transverse diameter of
6 centimeters.
Owing to the greater sizeof the leading dorsal vertebrae and to the
small dimensions of the ribs themselves the first three pairs of ribs have,
upon either side, greater intervals between them than any other members
of the series. These ribs are somewhat roundish in form, although
exhibiting a disposition to flatten at their vertebral ends as we pass
backward. In the fourth pair this flattening associated with an increased
width is pronounced, and from thence on is continued to include the
last pair. This accounts for the decrease in the width of the intercostal
spaces after passing the third pair of ribs, so that each intercostal space
is about equal to the ribs that bound it. There is very little difference
in the width of the ribs from the fifth to the thirteenth pair, inclusive,
7 Osteology of the Mammalia, 94-96.
162 : SHUFELDT.
and each one is nearly as wide at its sternal end, where it is joined by
‘a costal rib, as it is at its angle. Those forming the first pair are the
‘shortest in the series; the sixth, seventh, and eighth pairs are of about
equal length and are, at the same time, the longest ones of all.
Seven of the leading pairs of ribs are joined to the sternum through the
‘intervention of costal ribs; in the eighth pair the costal ribs are very long
“and attenuated, and lack but very little of meeting the distal extremity of
the mesosternum. . After this they rapidly shorten, the ninth, tenth, and
sometimes the eleventh articulating in sequence with each other’s lower
‘borders; the twelfth and thirteenth are thus joimed by a ligamentous
‘membrane only, and are practically floating costal ribs. (Figure 17.)
The first pair of costals are the shortest of all that unite the vertebral
‘ribs with the anterior end of the presternum, occupying facets, one upon
either side, just behind where the clavicles articulate. Like all the others
they are’ curved, the concavity of the curvature looking forward... From
the first to the: last, or seventh, pair of costals this curvature continues,
although it is here principally, indeed, almost entirely confined to the
outer third of the bone, especially in the last two or three pairs. ‘They
become progressively longer as we pass backward, and all seem: to be
composed of true bone, although.a little elementary in character. ‘The
distal pairs of costals are still more cartilaginous, but there is evidence
of osseous tissue in all of them. At their sternal ends they articulate
upon facets situated between the joints of the presternum and meso-
sternum, the sixth and the seventh articulating at the distal end of the
posterior joint of the mesosternum. None of the costals ever articulates
‘with the xiphisternum.
All the thoracic ribs articulate with the dorsal venes in the way
usual among mammals and they present the common characters of these
bones. .They are somewhat narrower in some specimens (1) than in
others (2, 3), but wide or narrow, any single rib in mid-series varies but
little in its own width from angle to costal articulation. All»present the
usual curvature, although here it involves almost the entire continuity of
the bone and is most pronounced dorsad.
If we select a “true rib” of the eighth pair as an example we find that
its capitulum-is well developed; the elliptical double facet is rather large
and placed longitudinally on the bone. The “neck” is but moderately
constricted; the “tubercle” is-but feebly pronounced, and owing to the
short transverse process of the dorsal vertebra, is quite close to the
capitulum. The ‘fangle” is but very: faintly indicated, and is entirely
absent in the last three pairs of true ribs. . As in the rest of the series,
the “body” of the twelfth rib is very flat with rather sharp anterior and
posterior borders. These last in Steere’s specimen are far more rounded.
Posteriorly and at the same time dorsad, there is a faint groove running
down the border of this rib. It harbors in life‘the intercostal vessels and
SKELETON IN THE FLYING LEMURS. 163
nerve, while its borders give attachment to the internal and external
intercostal muscles.
A very shallow concavity, or pit, occupying the ventral end of all the
true ribs, is intended for articulation with the outer extremity of the
corresponding costal rib.
Between the head and tubercle in most of the true ribs of this animal
we meet with a single nutrient foramen, usually upon the posterior aspect
of the bone. It is extremely minute in some of the ribs and varies some-
what in locality.
Cynocephalus possesses an ordinary and rather stout sternum, the parts
consisting of spongy bone overlaid by an extremely thin outer covering of
compact tissue. As usual in most mammals it is divided into the pre-
sternum (manubrium), the mesosternum (gladiolus, etc.), and the
xiphisternum (ensiform cartilage, or xiphoid appendage, etc.). Some-
times the parts of the mesosternum are designated as sternebre, the whole
being frequently called the “breast bone.” (Figure 17.)
The presternum is here short and trihedral in form, with its blunt
third angle situated mesially, and articulating in life with the anterior
end of the first sternebra of the mesosternum. Its outer anterior angles
are for articulation with the first pair of costal ribs. The sharper antero-
mesial-angle has, running between it and the distal end of the bone, a
low mesial raised crest which stands between the lateral aspects of this
joint of the sternum. Dorsally it is flat, while anteriorly the triangular
surface is very moderately concaved. Its longitudinal diameter averages
about 8 millimeters, and it is scarcely any wider at its widest part in
front.*®
Passing to the mesosternum we find it composed of four sternebre
closely resembling one another in form, and differing but little in the
matter of size. They are vertically compressed, smooth bones, narrower
at their middle than at their extremities, and in life articulate with each
other in the manner usual among mammals. They average about 4
millimeters in width, and rather more in length, the anterior one being 5
millimeters long and the third or longest one about 8 millimeters long.
They present the usual facets at their anterior and posterior angles for
articulation with the costal ribs.
The xiphisternum varies considerably in form, although it may be
described as a cartilaginous appendage, about as long as the third ster-
nebra. Occasionally it appears to be in two bits, one behind the other,
the anterior one exhibiting a very faint disposition to ossify. Viewing
the thorax from in front, it will be noticed that in most specimens the
The presternum in Oynocephalus is entirely different from that bone as we
find it in the mole (Talpa europea), as will be seen by examining Flower’s
figure of the latter. Osteology of the Mammalia, figure 34.
164 SHUFELDT.
sternal ends of the seventh pair of costal ribs articulate with each other
in the mesial line, and at the same time with the distal end of the last
sternebra. The xiphisternum is united to the mesosternum at the dorsal
aspect of this triple articulation; this is an unusual arrangement among
mammals, possibly not existing in any other known species. It is entirely
different in Talpa, and very probably in other insectivores.
In the articulated skeleton the xiphisternum is about opposite the tenth
dorsal vertebra, and the entire sternum has an average length of 4.5
centimenters.
[To be concluded.]
ILLUSTRATIONS.
PLATE A.
Skeleton of a flying lemur. By permission. Reduced. From the mounted speci-
men in the collection of the United States National Museum.
Pate I.
Fic. 1. Basal aspect of the skull of Cynocephalus ; lower mandible removed, and
a few teeth missing. Adult. Very slightly enlarged. Specimen from
Professor J. B. Steere.
2. Left lateral view of the skull of Oynocephalus, with lower mandible
articulated im situ, and the dental armature complete. Hyoidean ap-
paratus removed. About adult. Very slightly enlarged, and in same
proportion as figure 1, A specimen from the Bureau of Science, Manila,
12) dh
Prate II.
Fic. 3. Superior aspect of skull of Cynocephalus, lower mandible removed. Same
specimen as shown in figure 1 of Plate I. Exact natural size.
4. Lower mandible of Cynocephalus seen upon direct superior view. Dental
armature complete. This jaw belongs to the skull shown in figure 3.
Exact size of the specimen.
Left scapula of Cynocephalus seen upon direct ventral view, and natural
size. The absence of the superior angle, and the foraminal vacuities
in the blade are normal. The rounded superior angle of the right
scapula in this specimen is perfect. The bone belonged to the same
individual from which the skull and mandible were taken shown in
figures 3 and 4.
6. Left femur of Cynocephalus seen upon anterior view and slightly enlarged.
Note the almost entire absence of the pit for the ligamentum teres.
From the same specimen as figures 3, 4, and 5.
7. Lumbar vertebre of Cynocephalus, being the third to the seventh, inclusive,
and seen upon left lateral aspect. Natural size; from the same speci-
men as the other bones in this plate.
SH
165
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Vou. VI AUGUST, 1911 No: 4
NEWLY DISCOVERED BREEDING PLACES OF PHILIPPINE
: SEA BIRDS.
By Dean C. WORCESTER.
Gulls and terns in considerable variety have long been known from the
Philippines. Brown boobies, too, have been recorded by various ornitho-
logical collectors, but only one specimen of the red-legged booby, and
that an immature individual, had been collected in the Islands prior to
June 25, 1910, on which date, when crossing the Sulu Sea between Ka-
lusa Island and Puerto Princesa, Palawan, I saw a large flock of these
birds hoyering oyer a school of fishes. I had the captain change course .
slightly so as to take the steamer near them, but they dispersed before
us. Several individuals flew within long shotgun range of the ship and
I had the good fortune to bring down a fine, adult specimen which fell
into the sea but was recovered by stopping the steamer and lowering a—
boat.
On July 13, 1910, on which date I was exploring the islands in Green
Island Bay on the east coast of Palawan when I was heading for Reef Is-
land, I saw, on the starboard bow, a sandbar rising not more than a meter
above the sea, the tide at that time being full. While I was examining
it through my field glasses, a large flock of terns suddenly rose from it,
and after circling for a few moments settled again. Although the
breeding season for most birds was then well over, I was at a loss to
understand why these terns should be gathered in such numbers upon a
perfectly bare sandbar unless they had eggs or young there, so ordered
the steamer stopped and a boat lowered, and proceeded to investigate.
104558 167
168 WORCESTER.
The terns did not again take wing until we were close in shore, and
then refused to leave the immediate vicinity of the reef, circling close
over our heads. Nearly all of the individuals were black-naped terns,
Sterna melanauchen Temminck, but by pure accident I Jalled a single spec-
imen of the oriental roseate tern, Sterna gracilis Gould, which had never
before been taken in the Islands. By watching sharply, I was then able
to pick out and kill two additional specimens, recognizing them in flight
by their red legs. ;
We found numerous eggs on the reef. They were deposited singly or
in pairs in slight depressions in the sand, lined in a number of instances
with bits of sea shell and of white coral.
So far as I am aware, this was the first time that terns have been
found breeding in the Philippines.
On August 24, 1910, I joined Gevernor-General Forbes and the Sec-
retary of War on board the steamer Rizal at Capiz, Panay, and was
greatly interested to learn that on their way from Jolo to Puerto Prin-
cesa they had landed on Bankoran Island in the middle of the Sulu Sea,
finding great numbers of brown and red-legged boobies and some of the
greater frigate birds, as well as a few terns. They had obtained speci-
mens of all the species observed and had put them in cold storage so that
I was able to make positive identifications. They told me that there
were many nests in the trees and on the ground, but that only one egg
had been obtained. Upon examination I found that the egg was ob-
viously that of a booby, but whether of a brown or a red-legged booby it
was impossible to say.
On September 16, 1910, I had occasion to leave Manila on a trip to
the west coast of Palawan and subsequently passed through Balabac
Strait and sailed north along the chain of islands and shoals which
extends in a generally northeasterly direction through the Sulu Sea.
Bankoran Island was reached early on the morning of September 22.
Fortunately the weather was calm and we were able to land at the south-
western end of the island at 6 o’clock. From the steamer we had seen
immense flocks of boobies circling about the island, which is covered
throughout nearly its entire extent with trees, but has at its western end
sand-spits, partially overgrown with grass and bushes, while at low tide
rough masses of coral rag are left exposed by the receding water.
We at once discovered that the red-legged boobies, Sula piscator (Lin-
nus), were nesting in the trees, while the brown boobies, Sula lewco-
gastra (Boddaert), were nesting on the ground. “A few moments’ ob-
servation sufficed:to show that a number of red-legged boobies, which
we found in, or close to, nests upon the ground, were not their owners as
we had at first supposed, but were stealing nesting material from them in®
the absence of the brown boobies which had built them.
- With very few exceptions the nests on the ground contained no eggs.
BREEDING PLACES OF SEA BIRDS. 169
We soon discovered this to be due to the fact that two boat loads of
Moro egg-hunters had on the previous afternoon removed every egg
from the ground nests. Their boats were still anchored on the shoal to
the north of the island and were found to contain both boobies’ eggs and
sea turtles’ eggs in large numbers.
Apparently they had been too lazy to climb the trees after the eggs of
the red-legged boobies, some of which we were, therefore, able to collect.
The Moros assured us that by noon there would be plenty of fresh eggs
in the nests of the brown boobies, and this proved to be the case. The
boobies of both species were so tame that we experienced no difficulty in
catching alive as many as we needed for specimens, and we were also able
to secure a yery interesting series of photographs, and to observe closely
the nesting habits of the birds of both species. The male and female —
brown boobies were readily distinguished by the fact that the former had
the bare skin at the base of the bill and on the throat dark blue, while
in the latter it was bright lemon yellow.
The ground nests of the brown boobies were made of bits of rotten
wood, dead leaves, small branches, and twigs to many of which green
leaves were still attached. In fact we saw the birds breaking such twigs
from the trees. The female usually remained sitting bolt upright in
her nest, while the male brought nesting materials which he turned over
to her. These she promptly put in place, not infrequently lifting and
putting down repeatedly a given leaf, twig or bit of punky wood until she
had placed it just to suit her. Occasionally the materials brought by
male birds were rejected, and as a rule when the latter endeavored to put
any material in place in the nest, as was sometimes the case, it was
thrown out by the females, which were evidently determined to construct
their houses in strict accordance with their own ideas and to keep the
male birds under proper discipline.
In many cases the nests were in close proximity to each other and the
male birds were constantly trying to steal materials from other nests.
This led to vigorous vocal protest from the rightful owners and not
infrequently to rough-and-tumble fights as well. The fights were all
of short duration and quite bloodless. In no instance could we see that
one booby really injured another.
The red-legged boobies not only stole nesting materials from their
brown relatives, but quarreled shamefully among themselves.
_ Every bird which attempted to fly through the air with a fairly size-
able branch in its mouth was set upon by half a dozen others, which, in
their efforts to make it drop its burden frequently drove it to the ground
where it was vigorously mauled until it relaxed its hold upon the branch.
Some other bird then attempted to fly off with it and was set upon in
turn. These contests seemed always to end when a lucky individual
succeeded in getting to its nest with the coveted branch:
170 WORCESTER.
Both brown and red-legged boobies rose readily from the ground, and
flew among the trees with greater skill than one would have expected
them to display, but if caught in grass or brush they were very helpless.
Only a single frigate bird was observed, and this individual promptly
left the island on our arrival.
The eggs of the two species were indistinguishable. Hach had a white,
chalky outer layer, with a harder underlying layer which was very light
blue in color. The female brown boobies were most reluctant to leave
nests which contained eggs, and in some instances would not do so until
actually pushed off. Upon the near approach of any member of our
party, females which were sitting upon eggs manifested their uneasiness
and nervousness by croaking and by picking up and laying down bits
of nesting material. In a number of instances they displayed great
courage, staying by their eggs and pecking vigorously at the hands
of those who attempted to dislodge them. When taking photographs
with a Graflex camera I had no difficulty in getting within four feet of
nesting birds.
In the course of the morning a fresh breeze sprang up and the tide
which had been low when we landed rose so that we could not reémbark
on the windward side of the island but had to send the boat around
to the leeward side. We returned to the steamer at a quarter past
twelve and I requested the captain to sail for Tub-bataha, thinking
we might find sea birds on one or another of the several small islands
which rise from this extensive shoal. The captain, however, objected,
as we should necessarily have arrived at night. The position of Tub-
bataha is not definitely known, and there are a number of bad outlying
shoals, so that he did not deem it prudent to stand on and off in the
dark. As an alternative he suggested that we visit Maeander Reef,
where, according to the sailing directions, sea birds had been “seen in
large numbers.
At 4.30 in the afternoon the steamer changed course sharply to the
south. Maeander Reef had been sighted from the masthead considerably
to the south of the point where it is shown on the chart. We reached it
in half an hour and found it to be a mere sandbar about 200 meters
long by 150 wide, rising not more than two meters above the water.
It is surrounded by an extensive shoal over which we were forced to
wade and is absolutely devoid of vegetation. Drift wood lodged at
its highest point showed that the waves break clean over it in very
heavy storms, in spite of the shoal which one would suppose would prevent
any such result. : :
While still at a considerable distance, we saw through our glasses
flocks of birds flying over the reef, and regiments of brown boobies
sitting in long lines upon the shore. As we drew nearer we made out
groups of northern Bergius’s terns, Sterna boreotis Bangs, with young
BREEDING PLACES OF SEA BIRDS. lege
which were big enough to run about freely and to take to the water
upon our nearer approach. Upon walking up the steeply shelving
sand beach we beheld a wonderful sight. Hnormous numbers of sooty
terns, Sterna fuscata Linneus, were standing on the sand in great
groups, containing fully adult birds in breeding plumage, immature
birds which were dark brown or black with some white-spotted feathers,
young still partially in the down but with wings feathered out, and
freshly hatched chicks colored so like the sand about them that when
they crouched flat upon it, with outstretched necks and extended wings,
they disappeared from view before one’s yery eyes. Eggs were scattered
around in large numbers, but many of them were bad ones which had
failed to hatch. Large solemn-looking chicks of the brown booby,
still in the down, but apparently heavier than their parents, were
sitting about in considerable numbers. ‘There were also numerous breed-
ing groups of northern Bergius’ terns, with small chicks and eggs, in
addition to the groups previously referred to which contained young
big enough to run about actively.
Immediately after landing we observed several noddy terns, Anows
stolidus (Uinneus). A shot fired at one of these caused thousands
upon thousands of birds to take wing. We worked actively until dark,
taking photographs and securing specimens of the several species of
birds in different plumages, and then returned to the ship heavily ladened
with valuable ornithological spoils.
I could not make wp my mind to leave the reef without taking ad-
ditional photographs. The light at the time of our arrival was very
weak and it had faded rapidly so that I feared that many of the plates
which we had exposed would be failures. Therefore, we stood on and
off through the night. The current drifted us some four miles to the
northward but we picked up the reef from the masthead at 5.30 the
following morning.
On the afternoon of our arrival the birds had been kept in constant
motion by the sailors who were running about in search of turtles’
eggs, and by other members of our party who were looking in vain for
insects or plants.
Our two ornithological collectors remained on board to care for the
material obtained the previous day, and I limited the landing party to
the Director of the Bureau of Science, one Filipino collector, two sailors,
and myself.
With difficulty the sailors were convinced that it was to their interest
to sit down and keep still. I then got an opportunity to obtain some
very interesting photographs. There were a few red-legged boobies
on the reef, but so far as I could see they were not breeding. A number
of brown boobies had deposited their eggs in hollows in the sand, as
there was no nesting material available on the island, except a little
©
172 - | WORCESTER.
decayed wood laboriously. torn from the few tree trunks which had
drifted on to reef. One enterprismg female had actually dug out
enough punk to make a hollow in a log and had deposited her two eggs
therein.
Although the number of eggs laid by one ae seemed to be quite.
uniformly two, in only one instance did I see: a brown booby caring
for more than one young one. Photographs of the boobies could be
taken at any desired distance.
I found it possible to walk directly among the sooty terns.. Although
they at first flew away from my immediate vicinity they promptly
returned again. The nesting groups of the northern Bergius’s terns
proved much more difficult to approach, but by the exercise of a little
care and patience I was able to get quite satisfactory photographs of
one such group. I had never previously known that the birds of this
species had the power of erecting the black feathers of the head so
as to form conspicuous crests. One of the photographs reproduced
(Plate V, figure 1) shows clearly that this is the case. Shortly before
10 o’clock a strong breeze sprang up from the southwest. Immediately
every sooty tern on the island, except a few of the downy chicks,
faced the wind which proved to be the forerunner of a heavy shower.
When the rain was almost upon us Doctor Freer fired at a frigate bird.
Thousands of terns took wing but instead of circling widely as they had
previously done when alarmed, held themselves stationary in the air,
hovering for a moment over their eggs and young, but almost im-
mediately dropping upon them again. After the rain began to fall the
birds which were incubating eggs refused to leave them until actually
pushed away, pecking savagely at the hands of intruders.
I greatly regretted the coming of this shower as I wished to secure
more photographs showing the habits of the big booby chicks. When I
first landed I saw a number of chicks stretched out flat on the sand
with wings extended and heads doubled back under their necks. I thought
at first that they were dead but found upon touching them that they were
very much alive. I then jumped to the conclusion that they were
trying to hide, as did the little terns, but after further observation con-
vinced myself that they were merely sleeping. In each instance when I
attempted to turn the camera on them at short range they woke “UP and
hopped awkwardly away.
As there was no sheltering vegetation of any kind the heat upon the
reef became intense as soon as the sun got well up. The booby chicks
promptly took advantage of the shadows cast by older birds, often coming
up from behind and flattening themselves on the sand with their heads
stretched under the tails, or even between the legs, of their mothers.
As it was obviously unsafe to remain on the reeef a moment after the
sea began to rise, we reluctantly turned our backs on one of the most
BREEDING PLACES OF SEA BIRDS. 173
extraordinary scenes which I have ever witnessed, waded out to the edge
of the shoal, took the boat to the steamer, and sailed for Cayilli Island,
where we arrived the next morning shortly after daylight.
Just before we left Maeander Reef three man-of-war birds had sud-
denly appeared, hurrying in before the on-coming storm, and Doctor
Freer had succeeded to our great ‘satisfaction in killing two of them.
When discussing our good luck on board the steamer the following even:
ing it was suggested that it only remained to find oa birds and petrels
breeding on Cayilli!
Just as I was going down to breakfast in the morning my son came
running to tell me that frigate birds were hovering low over the steamer,
and upon ascending to the upper bridge deck I discovered several in-
dividuals within easy range. Within the next few moments I shot nine,
of which eight were recovered. By this time we could see frigate birds
in large numbers flying over Cavilli Island, which like Bankoran Island,
is heavily forested. Furthermore, we saw in increasing numbers, birds
which we at first took for petrels, and it really began to look as if the
wish which we had expressed the night before was to be fulfilled.
Immediately after breakfast we landed in the ship’s small boat, having
as usual to wade for a long distance over a shoal before reaching the
beach. On our way we shot a number of specimens of the above mentioned
small petrel-like birds, which proved to be of the genus Micranous. No
representative of this genus had ever previously been recorded from the
Philippines. Comparison with specimens in the United States National
Museum shows that this is a species closely allied to Micranous leucoca-
pillus (Gould). It is described in this Journal as Micranous worcestert
McGregor, sp. noy.t
Upon arrival at the beach, Mr. McGregor, the government ornithologist,
set off rapidly for a sand spit at the east end of the island where
he expected to find Micranous breeding, while the rest of us went directly
into the forest where I hoped to be able to kill some of the frigate birds
which were flying just above the tree tops. To my amazement, I found
countless thousands of Micranous nesting in the trees. A single cartridge,
loaded with a small charge of dust shot, brought down seven perfect
specimens. Sailors were sent up the trees but found most of the nests
empty. We had arrived too late to get eggs in any numbers. An adled
egg was, however, obtained, and we also secured several well-grown
nestlings which were photographed at short range. The frigate birds
had apparently finished nesting but immature birds were present in large
numbers.
Red-legged boobies were Fine in the trees, but we aad not see a
single brown booby on the island.
*This Journal, Sec. D (1911), 6
174 WORCESTER.
Male frigate birds, Pregata aquila (Linneus), were flying about with
their scarlet throat pouches puffed out like children’s toy rubber baloons,
and a photograph was secured of a fine male which came down wounded
and kept its throat pouch partially inflated.
Shortly before noon we returned to our steamer taking with us a
splendid series of specimens of the frigate bird and of Micranous, and
also a number of wood rats which were extraordinarily abundant.
During the lunch hour we ran as near as possible to the Arena Islands
of which there are two rising from an extensive shoal. Here we found
two frigate birds; also a number of brown boobies nesting on the ground.
We decided, however, that it was best to return to Cavilli Island and
collect carefully selected specimens of frigate birds in order to complete
a series showing fully the immature and adult plumages.
This we were able to do. A wounded bird which fell into the sea near
shore served to attract others in large numbers so that we could select
our specimens at will. We also obtained a good series of immature red-
legged boobies. These birds displayed a great interest in us both when
we approached and when we left the island and in several mstances
attempted to alight upon us or our boat.
Just before dusk as we were leaving for the steamer we witnessed an
extraordinary scene. Large numbers of red-legged boobies which had
apparently been fishing all day began to return, bringing fish to their
nesting mates and to their young. The frigate birds promptly formed
a skirmish line and, singly or in pairs, attacked all comers, compelling
them to give up their fish. Some of the boobies, possibly sophisticated
individuals which had learned wisdom by experience, actually handed
their fish over to the frigate birds and so escaped without much drubbing,
but less experienced or more obstinate individuals which at first refused
to disgorge were vigorously punished until they changed their minds and
threw up their fish which were most adroitly caught in the air by their
piratical enemies. In one instance two frigate birds set upon a booby,
one of them attacking him from above and the other flying below to
catch the fish which he dropped, and getting five out of seven. Soon the
incoming bobbies began to arrive in flocks and the frigate birds were not
able to set upon them all, so that many individuals got through to the
island. Once among the trees they were left in peace.
A trip should be made to Cavilli Island earlier in the season when
Micranous and possibly also the frigate birds will be found mating.
On June 23, 1911, I sailed from Manila with Governor-General Forbes
- and others on a trip to the Calamianes Islands, Palawan, the Sulu Archi-
pelago, and Mindanao. On the evening of June 28 we left Puerto Prin-
cesa for Sibutu and Sitanki, and as the weather was unusually calm
decided to go by way of Tub-bataha Reef which I had never previously
succeeded in visiting.
BREEDING PLACES OF SEA BIRDS. 175
Harly the following morning we reached that reef finding, near its
exterme northern end, a low flat sandy island called Usong. It is some
400 meters long by 150 wide. The sailing directions state that this
island has upon it a rock 20 feet high, as well as some trees, but this
is not the case. A boat belonging to some turtle hunters was anchored
just off the beach and they had erected on shore a small hut thatched
with nipa-palm leaves. Doubtless some timid navigator passing the
reef at a distance mistook such a house for a rock.
There was no vegetation on the island except a few plants of pursley.?
There can never haye been any trees there as the waves evidently dash
clear across it during violent storms.
Brown boobies in enormous numbers were nesting in the sand.
Near the center of the island there was a large colony of black and
white boobies, which we at first mistook for red-legged boobies. Presently,
however, the Governor-General called my attention to the fact that they
were not red-legged. On the contrary their legs, feet, toes, and nails
were of a very dark lead color. Indeed they were almost black. Their
bills were dull yellow and the bare skin at their bases was of the color
of that of the feet and legs. I have since identified these birds as belong-
ing to the species Sula cyanops (Sundey.), a species not previously
“recorded from the Philippines.
There were numerous noddy terns, Anous stolidus (Linnaeus), on
the island and they were nesting on the ground among the pursely plants.
We did not find any of ‘them nesting on the bare sand.
There were also a number of large and interesting groups of northern
‘Bergius’s terns. The egg hunters had gathered the terns’ eggs into
heaps preparatory to carrying them off. I compelled these misguided
individuals to leave the birds undisturbed throughout the day, and with-
in a short time the terns had scattered the heaps of eggs over the sand
and were incubating as busily and contentedly as if nothing had
happened to disturb them. —
After gathering numerous typical eges for the collection of the Bureau
of Science, shooting a number of fine specimens of the breeding birds,
. and taking a series of photographs, we sailed to the south skirting
the eastern edge of Tub-bataha Reef until the small island on Black
Rock Reef hove in sight. Meantime we had passed near a second
small sandy island on Tub-bataha Reef. It seemed to be covered with
brown boobies, as was the island on Black Rock Reef. We landed on
the latter, finding numerous nesting brown boobies and northern. Ber-
gius’s terns, but nothing else.
2 Portulaca oleracea I..
Fig.
Fig.
Fig.
Fic.
Fic.
Fia.
ILLUSTRATIONS.
(Photographs by Worcester and Cortez.)
PLATE I.
Brown booby; Sula leuwcogastra (Boddaert) .
Prate Il.
. Female brown booby with two large chicks. Maeander Reef.
. Brown booby with nest and egg. Bankoran Island.
Prate Ill.
. Nest and egg of red-legged booby, Sula piscator (Linneus). Bancoran
Island.
. Red-legged boobies nesting. Bankoran Island.
Prate IV.
. Sooty terns, Sterna fuscata (Linneus). Maeander Reef,
2. Group of sooty terns nesting. Maeander Reef.
PLATE V.
. Northern Bergius’s terns, Sterna boreotis Bangs, nesting. A sooty tern
in the foreground. Maeander Reef.
». Eggs and young of northen Berguis’s tern. Maeander Reef.
Pirate VI.
. Boobies on Usong Island. Tub-bataha Reef.
2. A group of sooty terns, chiefly immature. Boobies in the background.
Pirate VII.
. Young of Micranous worcesteri McGregor, sp. nov. in nest.
2. Bankoran Island from the north.
PLATE VIII.
Sula cyanops (Sundey.). Usong Island, Tub-bataha Reef.
177
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THE PHILIPPINE JOURNAL OF SCIENCE,
1). General Biology, Ethnology and Anthropology.
Vol. VI, No. 4, August, 1911.
HYBRIDISM AMONG BOOBIES.
By Drawn C. WoRCESTER.
On the morning of June 29, 1911, while observing the boobies on
Usong Island at the northern end of Tub-bataha Reef, I saw and shot
an extraordinarily colored individual which had every appearance of
being a hybrid. This led me to walk the length of the island several
times, carefully searching among the thousands of nesting birds for other
similar individuals. I found two, and J am satisfied that there were
no more.
What interested me still more was to find a female Sula cyanops mated
with a male Sila leucogastra. he latter was in full breeding plumage
and his sex was conclusively proved by the color of his legs and feet
and of the bare skin of his head.
The strangely matched pair had a nest to which they promptly returned
whenever I drove them away. It contained no eggs, but this was
a lack which was evidently soon to be remedied! There was no possible
doubt that the birds were mated, and it seems not improbable that the
three hybrid individuals observed, all of which proved to be fully adult,
may have been their offspring. -
179
"FON ‘TA “TOA “IOS ‘NUNOL “‘TIHg] [ Sara00g] DNOWY WSIGINAAPT : UAGSTOMOAL
ILLUSTRATION.
Prats I. Portion of colony of nesting boobies on Usong Island showing a fe-
male Sula cyanops (Sundey.) mated with a male Sula leucogastra (Boddaert.)
(Photograph by Worcester.)
181
"pON ‘TA “IOA “IOS “NUDOL “11H ] ['Saulg. Vag JO saovId DNIaCWAN : UILSTOVO MW
WORCESTER : BREEDING PLACES OF SEA BIRDS. ] [PHIn. JOURN. Scr., Vou. VI, No. 4.
PLATE Il.
WORCESTER: BREEDING PLACES OF SEA BIRDS. |] [PHiIn. Journ. Scr., Vou. VI, No. 4.
[PuHIn. JourN. Scr., Vou. VI, No. 4.
Ds. ]
S OF SEA BIR
BREEDING PLACE
STER:
WORCE
Fic. 1.
Fia. 2.
IV.
PLATE
WORCESTER: BREEDING PLACES OF SEA BIRDS. ] (PHIL. JouRN. Sci., Vou. VI, No. 4.
mS
ese 0
PE ene 3 ee eee
er
WORCESTER: BREEDING PLACES OF SEA BIRDS. | [PHiIn. JOURN. Sci., Vou. VI, No. 4.
Fic. 2.
PLATE VI.
WORCESTER: BREEDING PLACES OF SEA BIRDS. | [PutIn. Journ. Scr., Vou. VI, No. 4.
Fic. 2
PLATE VII.
"IA St7w41da
"FON ‘IA “I0A “IOS ‘Nuno “TIHg] : [sauig vag 40 sdovtg DNIGaGUg : ULSAOUOW
THE PHILIPPINE JOURNAL oF SCIENCE,
D. General Biology, Ethnology and Anthropology.
Vol. VI, No. 4, August, 1911.
RECORD OF A PUFFINUS NEW TO PHILIPPINE WATERS AND
DESCRIPTION OF A NEW SPECIES OF MICRANOUS.
By RicHarp C. McGREGoR.
(From the Section of Collection of Natural History Specimens, Biological Labor-
atory. Bureau of Science, Manila, P. f.)
Puffinus chlororhynchus Gould.
A female of this species of shearwater was captured aboard the United
States Army transport Crook, July 30, 1910, off the Zambales coast,
Luzon. Length, 230 millimeters; extent of wings, 960. Legs and feet
pale bluish white, brown along the outer side; bill dark horn-brown; iris
brown. No. 13172, Bureau of Science collection. Collected by Dean
C. Worcester. Dr. Charles W. Richmond of the United States National.
Museum has examined this specimen and agrees with my identification
of it.
Micranous worcesteri sp. nov.
Type.—No. 7300, adult male, Bureau of Science collection. Collected
on Cayilli Island, Sulu Sea, Philippine Islands, September 24, 1910,
by Dean C. Worcester, R. C. McGregor, and A. Celestino. Bill black;
tarsus and toes dark, reddish brown; nails black. Length, 355 milli-
meters; wing, 222; tail, 120; exposed culmen, 43; bill from nostril, 31;
tarsus, 21; middle toe with claw, 38.
Specific characters.—This species is undoubtedly closely related to
M. leucocapillus Gould, but it differs in having a darker, grayer tail, and
somewhat longer toes. ”
Immature—lLarge nestlings with rectrices not extending beyond the
toes resemble the adult in plumage, but the forehead, crown, and nape
are nearly pure white instead of ashy gray.
Nest and egg—The nest of Micranous worcesteri consists of a mass
of leaves with little or no depression for the egg, and is situated on the
branch of a tree. A nest is about 10 centimeters in diameter. The
only egg collected by us contained a dead chick and measures 46 by 27
104558——2 183
184 M’GREGOR.
millimeters. Color dull white with a few, large spots of burnt umber
about the larger end.
Remarks.—As described by Worcester this species is abundant on Ca-
villi Island during its breeding season. Several of our specimens have
been examined by Dr. Charles W. Richmond to whom J am indebted
for notes on the various species of the genus. The species is named
for Mr. Dean C. Worcester through whose interest and efforts it was
discovered.
THE PHILIPPINE JOURNAL OF SCIENCE,
D. General Biology, Ethnology and Anthropology.
Vol. WAG No. 4, August, 1911.
THE SKELETON IN THE FLYING LEMURS, GALEOPTERIDA. =«
By R. W. SHUFELDT.
(Washington, D. C.)
(Concluded. )
THE SHOULDER GIRDLE.
Comparative andtomists have observed great differences in the mor-
phology of the shoulder girdle among the various representatives of the
Insectivora, not finding this structure alike in any two families of the
order. Cynocephalus has the two bones composing it, the clavicle and
the scapula, remarkably well developed and in full proportions for the
size of the animal.
Making the usual articulations with the sternum and the scapula, we
find the clavicle to be a large, strong bone. Its extremities are enlarged
to support the articulatory facets. The shaft is stout with its continuity
of nearly uniform caliber, and presents two curvatures. About two-
thirds of its mesial length offers the least apparent curvature, being
slightly and uniformly bent so as to present the concavity to the front;
the remaining third of the bone makes a very decided curve to arrive
at its scapular articulation. ‘This part of its shaft is somewhat antero-
posteriorly flattened, or rather compressed, being nearly flat behind and
concave in both directions anteriorly. In the normally articulated skele-
ton, this curvature allows the clavicle to pass over the prominent coracoid
process of the scapula, and brings its outer extremity in articulation
with the external process of the two apophyses which finish off the upper
end of the acromion process of the scapula. In one of the specimens
from the Bureau of Science (2) the clavicle has a length of 3.6 centi-
meters while it is only 3.4 centimeters in the Steere specimen, and 3.
centimeters in the remaining individual (3). Therefore it averages 3.2
centimeters in length, and is about as long as one of the thirteenth pair
of true, or vertebral, ribs of the skeleton to which it belongs.
It is somewhat remarkable that the scapula in some specimens of
Cynocephalus does not fully ossify; this lack of ossification occurs in the
so-called “blade” of the bone, (Plate II, figure 5 (1): see explanation
185
Or Or
186 SHUFELDT.
of plates), while in others it is very complete and rather thick (2, 3).
Again, the scapula in different individuals is prone to vary in some of
its characters, but to no greater extent than we find among a series of
human scapule chosen from adults of the same sex and race. One of
the skeletons sent by McGregor (2) has the scapula thoroughly ossified,
quite perfect, and presenting all the characters of the bone as they occur
in our subject. It is here seen to be a distinctly triangular bone with
all its parts highly developed.
Facing upward and inward, the glenoid cavity is rather extensive;
the concavity is pear-shaped in outline, and the small end extends upon
the base of the coracoid process. From the glenoid cavity to the inferior
angle we have the external or axillary border, which here presents a
notable departure from mammalian scapule generally in being broad
and flat for almost its entire length to the lower point of the bone. This
flat border is of uniform width to its termination, that is about 4 milli-
meters, and appears as if it had been formed by bending that much
of the blade of the bone abruptly, at a right angle toward the spine,
thus creating a deep “infraspimous fossa,” but adding nothing to the
ventral aspect of the bone. The vertebral or internal border is not as
long as the axillary one, and its margin is only very slightly thickened
for its entire length. The two borders make an angle of 30° with
each other, and the angle thus formed, or the inferior angle of the
scapula, is here rounded off rather than acute; the sizable bit of the
apex, evidently formed from the usual independent center of ossification,
has not yet united with the blade of the bone.** The superior border,
extending from the inner base of the coracoid process to the angle
which in anthropotomy is known as the “superior angle,” is here sharp
and uniformly concave throughout its length. The superior angle
is about a right angle and is rounded as in most mammalhan scapule.
The superior border is only about one-half as long as the axillary one;
the vertebral border stands between the two in this respect. A supra-
scapular notch hardly exists in the superior border near the coracoid
process; indeed, although the greatest céncavity of the border here is
where it usually occurs, no such break in its continuity is to be dis-
tinguished. At its narrowest part the neck of the scapula measures
just 1 centimeter, and likewise this is the thickest part of the bone
antero-posteriorly, it being about 0.5 centimeter just within the glenoid
cavity.
“This indicates that the animal was still in a subadult stage when killed.
Complete union has taken place in the other two specimens (1 and 3) from which
we conclude that they are more advanced in age. In the human species it is not
until the sixteenth year that this epiphysis unites with the rest of the scapula at
this point.
THE SKELETON IN THE FLYING LEMURS. 187
Smooth and quite level, the subscapular fossa on the venter of the
bone exhibits hardly any muscular ridges, the only one of any prominence
being a mere indication of such extending from the neck to a mid-point
on the vertebral border. Even this may be absent from some specimens.
The coracoid process is represented by a straight, somewhat flattened
rod of bone, that may attain a length of nearly 1.5 centimeters. It is
extensively attached to a raised base or pedicle at the junction of its
inner and middle thirds. This gives rise to a long and a short process,
the first assisting in the formation of the articulation for the-humerus,
and the inner and shorter one for ligamentous attachment. Its long-
itudinal axis makes an angle with the long axis of the acromion process
of about 60°, and an angle of about one-half as many degrees with the
plane of the scapular blade. Thus it will be seen that the coracoid is
not bifurcated as stated by Flower *° but simply produced both ways
from its base, in the same straight line.
Very conspicuously developed, the spine on the dorsum of the scapula
commences superiorly or, perhaps, what may be called externally, beyond
the glenoid cavity. Here it supports a large acromion process and a
metacromion; this is followed by a somewhat flattened pedicle to the
scapular neck, and from there on it becomes a thin lamina of bone which
gradually slopes away to a point near the middle of the vertebral border.
This osseous partition creates the supraspinous and infraspinous fosse,
-which are thus thoroughly defined. The latter is about twice the size
of the former, and lengthwise is bounded by the aforesaid spine on the
one hand and by the raised axillary, described above, on the other. The
scapula makes the usual articulations with the humerus and clavicle, and
has attached to it, either by origin or insertion, a number of important
muscles and ligaments.
THE PELVIS.
Beyond a few unimportant individual variations, the pelves (Plate
II, figure 8; Plate IV, figure 14, and Plate V, figure 17) of the three
specimens of Cynocephalus at hand present the same characters for
description. On the other hand this part of the skeleton differs widely
in its morphology among the Insectivora as a group, being long in some,
short in others, while in such genera as Sorea, Talpa, and Chrysochloris
a wide interval separates the pubic bones at the mesial line below, where
they usually unite.
When submitted to ordinary maceration in water the two ossa in-
nominata readily part company with the sacrum and with each other.
This happened in the case of the Steere specimen here shown in figures
Sand 14. One of the most striking features of the pelvis in Cynocephalus
* Osteology of the Mammalia, 253.
188 - SHUFELDT.
is its unusual length as compared with its width; the former being
about 8.7 centimeters and the latter 4.3 centimeters taken opposite the
acetabule.
Its articular surface for the sacrum is upon the inner side of the ium
about 1.7% centimeters from the “crest,” and covers an area of a little
more than 1 centimeter in length. Dorsally, this area projects as an
elongated, sharp crest; otherwise it is entirely confined to the surface
of the ilium proper and is faintly divided into two facets, a long posterior
or dorsal one, and a shorter oval one, parallel to and in close contact
with it.
Flower has stated that in “Galeopithecus” the symphysis pubis “is
long, as in the Carnivora, and becomes ankylosed.” ** He is certainly in
error in this statement for in all the specimens before me the symphysis
pubis is reduced to the merest contact of the bones, the area being very
small, and ankylosis never results. (See figure 14.) As he states, the
symphysis is long in most Carnivora, and this can be easily verified by
examining the pelvis of any of the Felide.
In the articulated skeleton of Cynocephalus the preacetabular portions
of the ilia are nearly parallel to each other and lie in a subtransverse
plane that makes but a slight angle with the longitudinal axis of the
lumbar and sacral vertebre. The anterior presacral portions of the ila
are directed upward, forward, and outward; the free extremities, which
are slightly enlarged and rounded, are about opposite the neural spines
of the vertebre. Thus it will be observed that all the preacetabular
portion of the pelvis affords but very slight protection to the contained
abdominal viscera; it does afford protection to some extent laterally,
and in conjunction with the sacrum and leading caudal vertebree, to a
greater extent dorsally.
It remains to say of the preacetabular part of an ilium that it is
sigmoid in form, and for the most part subcylindrical, although exhibit-
ing slight longitudinal flatness dorsally, mesially, and externally. This
rod-like part of the ilium gradually expands as it comes to the acetabulum
which it assists in forming. The latter is large, bemmg over 1 centi-
meter in diameter, and presents all the usual mammalian characters.
Its cotyloid notch is wide and rather deep; the cotyloid articular ring
is well developed; while the bone at the bottom of the cavity is often
very thin and always translucent. As usual, it is formed by the three
pelvic bones, the ilium, the ischitum, and the pubes, the sutures among
which have become entirely obliterated within the cotyloid cavity. In
fact the only sutural line that persists throughout the life of the in-
dividual among any of the three pelvic bones is the one between the
rami of the ischium and pubes. It is very distinct in all specimens at
hand, and probably is invariably present. (Figure 14.)
*t Osteology of the Mammalia, 320.
THE SKELETON IN ‘THE FLYING LEMURS. 189
The postacetabular portion of the pelvis is triangular in outline, the
acetabulum occupying one angle, the symphysis pubis another, and the
remaining one being at the tuberosity of the ischium, the last two bemg
rounded off. Upon its mesial aspect this part of the bone is uniformly
and moderately concave throughout, and entirely unmarked by elevations
or depressions. It encloses the very large, oval, obturator foramen, the
larger end of which is formed by the ischiopubic rami, where its margin
is sharp and clean cut, it being thicker and more rounded for the
remainder of the curve of this vacuity.
Externally the surface of the postacetabular part of the pelvis is like-
wise smooth, with its convexity corresponding to the concavity of the
mesial aspect. But one muscular line marks it, and that the usual one,
halfway between the obturator foramen and the tuberosity of the ischium,
indicating the limitations of the areas where arise certain important
muscles of the thigh, or more exactly, of the posterior femoral and
adjacent regions.
The external borders bounding this postacetabular portion of the
pelvis are rounded, smooth, and continuous for the pectineal line, con-
tinuous and slightly thickened for the ramal line, and considerably
thickened where formed dorsally by the ischium. The ischium presents
two prominent tubercles just without the rami of the cotyloid cavity.
They are separated by a shallow valley or notch, and the anterior one
has generally been designated as the “spine of the ischium,” at least, it
has been so-called in the human skeleton, where it affords surface tor the
origin of the gemellus superior muscle, the gemellus inferior arising
from the other tuberosity. These muscles among the lower mammalia
are generally known as the gemellus anterior and gemellus posterior,
owing to the direction of the longitudinal axis of the body.
THE SKELETON OF THE PECTORAL LIMB.
Both pairs of limbs in Cynocephalus are fully and powerfully devel-
oped, and they present many points of considerable interest. In writing
upon the subject of “the adaptive changes which take place in the seg-
ments of the limbs proper in yarious animals,” Flower ” has said:
In what may be considered the first stage of modification each segment of the
limb is simply bent upon the one above it. The proximal segments (humerus
and femur) remain unchanged in position, the dorsal surface still looking upwards,
and the ventral surface downwards, the middle segment is bent downwards, so that
its ventral surface faces inwards and its dorsal surface outwards; and ‘the
joints between these segments (elbow and knee) form prominent angular pro-
jections:
The third segment being bent to a greater or less degree, in the opposite direc-
tion to the middle one, retains much of its primitive position, the dorsal surface
being directed upwards and the ends of the digits pointing outwards. The rela-
tions of the pre-axial and post-axial borders of the limb are unchanged. No
* Osteology of the Mammalia (1885), 365, 366.
190 SHUFELDT.
mammal habitually carries its limbs in this position, although the climbing
Galeopithecus and the Sloths are not far from it. It is, however, very nearly
the normal position of some Reptiles, especially the Tortoises, although it is
ill adapted for anything but a very slow and clumsy mode of progression.
In Cynocephalus the humerus makes the usual articulations with the
scapula proximally, and the radius and ulna distally, that are seen among
mammals generally. ‘These articulations are in all cases extensive and
the joints very perfect anatomically.
The left humerus of the colugo (figure 15) offers the following points
for examination, some of which are better seen in the right humerus
(figure 16) from the same skeleton, this being due to the different posi-
tions in which the bones were photographed. Its characters, including
its length and to some extent its size, vary somewhat in various 1n-
dividuals. It is considerably shorter than the ulna or the radius; in
man it is the longest bone of the arm.
Viewed in its entirety, upon either its direct imner or outer aspect,
the humerus is seen to possess for its continuity the true “sigmoid curve.”
This curve starts at the head and terminates with the trochlear extremity.
Ignoring the prominent ridges its shaft is for the most part subeylindrical
in form, the principal departure being at the distal end which is ex-
panded to support the trochlez for the bones of the antibrachium. It is
uniformly smooth, and pierced by an oblique, nutrient foramen situated
about 2 centimeters distad of the articular part of the head, on the
posterior aspect.
The very conspicuously elevated deltoid ridge with its thickened edge
extends down the shaft, on its anterior aspect, for about one-third of its
length. It commences at the head and slopes away rather abruptly
distally. Its nearly straight free margin is almost parallel to the shaft’s
long axis, its sides being smooth. On the other hand the supinator ridge
is low, sharp, and thin, extending from the external condyle almost to a
middle point of the shaft, following accurately the lower sigmoidal
curvature of the latter, where it is gradually lost.
Among mammals we rarely meet with the humerus possessing a more
perfect head than it does in Cynocephalus, in which genus it is almost
a complete and entirely smooth hemisphere. For the most part its
articular surface is distinctly differentiated by its circular limiting line
and surrounding shallow groove or neck, the major part of which is seen
on posterior view. It reminds one of the humeral head of anthropotomy
and surmounts the shaft in a very similar manner (figure 15). Upon
either side of it the greater and lesser tuberosities are well developed, the
comparatively deep bicipital grooye passing the latter down the shaft and
the side of the deltoid ridge.
At the distal extremity of the bone, posteriorly, the olecranon fossa
is very deep and markedly defined. Its osseous base is thin, and may
THE SKELETON IN THE FLYING LEMURS. — 191
be perforated by a minute foramen. The internal and external condyles
are large, and pitted for the origin of certain muscles upon either side.
Above the internal condyle, anteriorly, there exists a delicate span of
bone of no great length. It passes, as a gently curved arch from the
condyle, obliquely toward the center of the shaft in a proximal direction
forming the supracondyloid foramen (figure 15), which gives passage
and protection to the median nerve and brachial artery. Where high
division of the brachial occurs, the nerve only, as a rule, passes under it,
but may be accompanied by the ulnar-interosseous artery.
The distal points of the trochlea and capitellum he in the same
horizontal plane to which the axis of the shaft is perpendicular. Hach
constitutes a prominent tuberosity separated distally by a well-marked
valley. Both in front and behind they rise to the same transverse line
on the shaft, ceasing at the distal boundary of the olecranon fossa poste-
riorly, and at the rather shallow depression intended for the ulna
anteriorly. The smaller tuberosity is flat upon its internal aspect, while
the capitellum for the radius is fully double the size with a roundly
convex articular surface. The average extreme length of the humerus
is about 10.2 centimeters.
Judging from the material at hand it would appear that when the bones
of the arm are normally articulated they admit of extreme flexion to a
far greater degree than they do of extreme extension, that is, extension
to the extent of bringing the long axis of the shaft of the humerus and
the ulna into one and the same straight line.
The radius is a very strong and nearly straight bone with enlarged
extremities and subcylindrical smooth shaft. It has an average extreme
length of 12.2 centimeters, or two centimeters greater than the humerus.
(Plate II], figure 9.) At its proximal end, the tuberosity for the in-
' sertion of the tendon of the biceps, is represented by a short longitudinal
crest, terminating in a groove near which we usually discover the opening
of a small nutrient foramen. Above the tuberosity the bone is some-
what constricted to form the neck of the radius and the latter is sur-
mounted by the head of the bone. The head is large, oval in outline,
and at its summit exists the rather deep concavity for articulation with
the capitellum of the humerus, while its marginal articulatory surfaee
for the ulna is about 2 millimeters deep. The outer lower third, or
more, of the shaft is flattened, forming a surface to which the distal
fourth of the ulna is firmly attached by ligament. Anteriorly, on its
expanded part at this extremity, we note the five conspicuous longitudinal
grooves intended for the passage of the extensor tendons as they go to
the hand. A sharp, peg-like, styloid process projects forward at the
outer side of the bone, but does not extend beyond the border over which
the extensor tendons pass. Internal to this process is a deep, elliptical,
transverse facet for articulation with the first row of bones of the wrist
192 SHUFELDT.
or carpus. The interosseous space existmg between the articulated ulna
and radius is long and narrow. From a study of the various articula-
tions of the antibrachium it would appear that during life the power
of pronation and supination must be somewhat limited.
A yery considerable amount of atrophy marks the development of the
ulna of Cynocephalus. To some slight extend this involves the head of
the bone, but is far more evident in the shaft. (Plate III, figure 9.)
On the whole the ulna is very straight from one extremity to the
other, straighter distally than represented in figure 9, where some cur-
yature is shown due to long maceration and subsequent drying. It has
an average length of 12.1 centimeters, or is practically of the same length
as its companion in the antibrachinm; it holds a postaxial position with
respect to the latter in the normally articulated skeleton. Among other
mammals, where the ulna is fully developed, it is a much longer bone
than the radius, due principally to its extension at the elbow. ‘This is
the case in man, in the Felide, and in many other mammals.
In the subject here under consideration the shaft of the ulna below
the head is considerably compressed from side to side and longitudinally
grooved for some little distance on its radial aspect, thus giving rise to
a sharp margin for the attachment of the interosseous membrane. From
its coronoid process to its distal apex the shaft contracts very gradually
and uniformly, and where the lateral flattening ceases it becomes more
or less compressed in the opposite direction, a condition which continues
to its distal end. On its outer surface this flatness is continuous from
one end of the bone to the other. In human osteology this outer surface
is described as the posterior surface of the ulna.**
Distally, the ulna is carried finally to a very sharp apex, or point,
which in the articulated skeleton is found just above the styloid process
of the radius. This point, together with the lower fourth of the bone,
is closely apphed to the shaft of the radius and is held there by a firm .
ligamentous attachment. That it ever actually ankyloses with the radius
is very much to be doubted, as ordinary maceration is quite sufficient to
separate the two completely. :
Proximally, the greater sigmoid cavity is circularly concave and not
very wide, although withal of good size; it is overarched by the olecranon,
which is here concave on its summit, uniformly thick from before, back-
ward, and pretty well fills the deep olecranon fossa of the humerus when
the limb is fully extended. There is not the slightest evidence of any
longitudinal division of the greater sigmoid cavity by a raised central
ridge as in man and other mammals.
Both the lesser sigmoid cavity and the coronoid process are well deye-
loped, the former being but very slightly concaved with its limiting
margin sharp and circular in outline. On the radial aspect of the head
* Gray’s Anatomy (1870), fig. 158.
THE SKELETON IN THE FLYING LEMURS. 193
a deep notch marks the boundary between the two sigmoid cavities, while
on the opposite side the limiting border is continuous and distinctly
circular in outline (figure 9). It is unnecessary to add that such an
ulna as Cynocephalus possesses takes no part in the carpal articulation.
The bones of the arm and forearm vary among the Insectivora to a
very marked degree; as, for example, among the hedgehogs, moles, and
shrews; and it is said that the ulna in Macroscelides and Petrodromus
is atrophied distally as in the colugo, but whether in these animals it
codssifies with the radius at that end may be open to question.
According to Flower:
Among the insectivora, the scaphoid and lunar (in the carpus) coalesce in
Galeopithecus, Tupaia, Centetes, Solenodon, Hrinaceus, and Gymnura, but in
most of the other forms these bones are distinct. A distinct os centrale is found
in all except Galeopithecus, Potamogale, Chrysochloris, and Sorea.™*
A very careful microscopical examination of two wrists, or carpi, in
two different specimens of the material at hand, proves beyond all question
that this statement, in so far as Cynocephalus is concerned, is quite in-
correct. All of the eight usual bones of the carpus are to be found in
this animal. . They are especially well developed in the manus of Steere’s
specimen, the one from the right pectoral limb having been very carefully
examined by me under a high-power lens. ‘There are four bones in the
proximal, and an equal number in the distal row.
Commencing at the inner end of the proximal row (ulnar side) we
find the pisiform to be represented by a rather large, elongate ossicle
that has a facet upon its mesial aspect merging with another distally, the
first articulating with the cuneiform, and the latter with the unciform,
as in the Felide and probably other mammals. Cuneiform, one-third
larger than pisiform, is of an irregular cuboidal shape, with a small facet
for pisiform, and a larger one for unciform and semilunar, the latter
being much concaved.
The semilunar is larger than any three of the other carpal bones taken
together, and is the only one of the wrist that articulates with the former.
This it dees with its large semi-ellipsoidal facet on its proximal aspect,
intended for the articulation at the distal end of the radius. Its outer
extremity also has a rather large, nearly circular, facet with which the
scaphoid articulates. Distally, the bone presents a raised, ridgelike, longi-
tudinal articulation for the trapezium; this is separated by a deep
eroove from a larger, central, likewise longitudinal, raised facet which
articulates with trapezoid and os magnum. More internally it offers a
small articular surface to the unciform. Thus it will be seen that the
semilunar articulates with no fewer than seven hones, viz: radius,
cuneiform.
*% Osteology of the Mammalia (1885), 289. This authority’s description of
the hand in the insectivores will hardly apply with accuracy to the colugo which
is unusually large. :
194 SHUFELDT.
unciform, magnum, trapezoid, trapezium, and scaphoid. Scaphoid is a
small compressed bone, but is larger than pisiform; it has but a single
articular facet covering its entire mesial aspect that articulates with a
similar facet on semilunar. It is connected with the trapezium by liga-
ment only.?°
Trapezium of the distal row is only exceeded in size by the unciform.
It is of an irregular cuboidal shape, with articular facets for the proximal
end of pollex metacarpal, trapezoid, and lunar. Above it, attached by
ligament only, we find the scaphoid, while mesially it presents a small facet
to the proximal end of index metacarpus.
Having very nearly the same form and _size, either being parallelepipedal
with respect to the former, the trapezoid and os magnum articulate with
each other and both with semilunar. ‘Trapezoid also articulates with the
metacarpus of index digit, as os magnum does with the same bone of the
middle finger.
Unceiform is a cube of irregular shape, the last carpal in the distal
row on the ulnar side, that articulates with lunar, cuneiform, and the
metacarpus of minimus digit, and the imner side of the base of the meta-
carpus of the fourth phalanx. Its palmar process is but feebly developed.
The manus of Cynocephalus is large in proportion to the size of the
animal, and exhibits in its skeletal morphology the chief uses to which
it is put, that is, being fitted to serve the purposes of climbing rather
than of prehension. It is especially long and rather narrow, being
armed distally with very efficient and powerfully hooked claws. It is a
pentadactyl member with a short pollex and four elongated digits. All
the phalanges composing these digits present the usual characters seen
among ordinary small mammals. Their shafts are very nearly straight
and quite cylindrical, while their distal extremities, or heads, support the
usual double trochlee for articulation with the phalanx next beyond
them in each instance. ‘The base of each of these long bones is larger
than its head and also presents an articular facet, which is oval and
concave to receive the head of the phalanx next behind it. The ungual,
or distal, joimts are entirely different and will be described further on.
The metacarpus consists of five bones; distally they articulate with the
five proximal phalanges of the digits and at their other ends with the
carpus In a manner already pointed out. Pollex metacarpal is very con-
siderably shorter than any of the others; mdex and minimus metacarpals
* In describing this bone as the scaphoid, the fact is known to me that among
rodents there are many wherein the scaphoid and lunar unite to form a single
bone; and further that a special ossicle, which has been described as occurring
on the radical side of the wrist, is of very considerable size in Castor. It has
also been said that in the beaver the scaphoid and lunar fuse to form one bone.
Notwithstanding these statements it is contended here that the scaphoid is
present in Cynocephalus, though embryology may disprove it, and two centers of
ossification may be shown to exist in the bone here described as semilunar.
THE SKELETON IN THE FLYING LEMURS. 195
come next in length and nearly equal each other in this respect. Medius
and annulus metacarpals are also of equal length and larger than any of
the other bones of this part of the hand. Pollex metacarpal is the stoutest
of them all and is about 1.6 centimeters long; minimus is also stout and
has a length of about 2.8 centimeters, while that of index is 5 millimeters
shorter. The shafts of the middle and ring, or the medius and annulus,
metacarpals are rather more slender, and each is nearly 3 centimeters long.
These metacarpal bones are slightly curved palmad and like the phalanges,
nearly parallel and very close to each other when the member is at rest.
Pollex has one short (1.5 centimeters), stout phalangeal joint and an
ungual joint; all the other digits have three each including the ungual
joints. Index is the shortest finger, minimus next, with medius and
annulus of about equal length. Not including the terminal joint, annulus
has a length of about 4 centimeters.
The ungual joints are all very much of the same form and size; the
largest being on pollex, index, and the next two digits, the smallest on
the little finger. Any one of them is very deep from dorsal to palmar
border, the latter being slightly concave, and the former powerfully con-
vex and a little jagged distally. From side to side one of these thoroughly
ossified joints is uniformly compressed to extreme thinness, while its
proximal border is somewhat thickened for the articular facet and for
tendinal insertions. At the postero-dorsal angle there is a very small,
concave, circular process for the insertion of the extensor tendon; palmad
to this is a large concave facet divided by a median longitudinal ridge.
This concavity is twice as deep as it is wide, and its surrounding border is
raised above the general surface. Palmad to this again, at the postero-
palmar angle, there is another very small process for the insertion of
the flexor tendon, while above this, beneath the lower border of the mid-
articular facet, are two minute foramina, side by side in the transverse
Ime. They lead into the bone and appear to be nutrient foramina.
The horny theca, fitting as a claw over one of these ungual joints, is
also powerfully compressed from side to side, and in form, with its very
sharp apex, resembles upon lateral view the upper bill of one of the
smaller typical falcons.
On the palmar aspect, beneath the articular joints of the metacarpals
and phalangeal bones, we observe in the case of each digit a pair of se-
samoids. These have the form of small compressed ellipsoids, the largest
ones being in the proximal tier of bones, whereas in the case of the
smaller pairs beyond, they are placed side by side in the transverse line.
Distally, the sesamoids are very minute and may be absent in the
index digit, between its first and second phalanx. They do not occur,
apparently, beneath the ungual joints at all. These sesamoids occur in
the hands and feet of other mammals, as certain carnivora, and even
in the tendons running to the toes on the plantar aspect of the foot in man.
196 SHUFELDT.
THE SKELETON OF THE PELYIC LIMB.
Proportionately, the pelvic limb of Cynocephalus is not as powerfully
developed as is the pectoral limb, though there seem to be exceptions to
this general rule. In Steere’s specimen, for example, the long bones of
the posterior limbs are fully as well developed as are the corresponding
ones in the anterior extremities. However, pes always seems to be weaker
and somewhat smaller than manus, and this is also evidenced in the
skeleton of these parts.
In the matter of proportions there are very marked differences in the
pelvic limbs of the three skeletons at hand. These differences may be
due to the fact that they came from different species, or if from the same
species, it may be due to differences in age or even sex. In any event
the Steere specimen was a much bigger animal than either of the
McGregor specimens, and one of the latter (3) is larger than the other
(2), though the characters throughout agree.
Two of the femora, selected as examples, show how marked these
differences are; for instance, the right femur of the Steere skeleton has
an extreme length of 12.3 centimeters, as compared with the extreme
~ length of the femur in the smaller of the two individuals from the Bureaw
of Science, which is only 11.1 centimeters. Then in the matter of actual
size the two bones are also in proportion to this difference in length,
the shaft of the femur in the first case being fully one-third larger than
in the second ease.
The description of the pelvic limb here given is from the right side
of the skeleton in Steere’s specimen, with occasional reference to the
other two individuals.
The femur (Plate II, figure 6), possesses a stout, straight, cylindrical
shaft, which is so smooth that even linea aspera is scarcely indicated
upon it. The proximal extremity of the bone presents an elegant, smooth,
hemispherical head, in fact so globular is it that it approaches the sphere.
This head is marked by no pit for the ligamentum teres; its boundary
is sharply defined in front; less so behind, where the articular surface
encroaches slightly upon the summit of the shaft of the bone. The axis
of the head and neck makes an obtuse angle with the axis of the shaft,
thus bringing the head above the latter’s summit. Conspicuous and
rough, the great trochanter curves slightly to the front, thus making the
neck of the bone very distinct behind it and the caput femuris. Minute
nutrient foramina may occur in this locality. On the postero-external
aspect of the great trochanter there is a well-marked pit, the so-called
trochanteric fossa, within which certain muscles are inserted.
Situated internally and at the same time posteriorly, and about 1 centi-
meter below the head, there arises the lesser trochanter, sometimes called
the tibial trochanter. It is bluntly triangular in form, and arises from
a substantial base. On the opposite side of the shaft, that is, on its
THE SKELETON IN THE FLYING LEMURS. 197
external border, and rather lower, there is still another and smaller
process, which is the third trochanter. Between these two projections
on the posterior aspect of the bone, the shaft is very smooth and partic-
ularly flat. No spiral line joins the greater and lesser trochanters on
the anterior surface of the bone, while posteriorly, the trochanteric line
is very feebly pronounced in the corresponding locality. Both these lines,
or intertrochanteric ridges, are very noticeable in the femora of many
other mammals, man included.
At the distal end of the shaft the two condyles are strong and thick.
They are almost exactly of the same size and neither one is lower on the
shaft than the other, as is sometimes the case among mammals where the
inner condyle is the lower of the two.
The smooth, convex, articular surfaces seen posteriorly on these
condyles are practically of exactly the same size, and they terminate in
the same transverse planes, both above and below. Between them is a
deep, sharply defined, intercondyloid notch, that terminates abruptly at
the lowest plane of the bone and superiorly in a similar manner on a flat
surface named in anthropotomy the popliteal space. Again, either the
internal or external condyle exhibits upon its outer surface a distinct pit,
or depression, wherein certain muscles arise or are inserted. One is about
as well marked as the other, as are the tuberosities that occur, one in
‘each case, above them. The one on the outer condyle is the outer tubero-
sity, and the other the inner tuberosity. Anteriorly, the intercondyloid
space is of a nearly quadrilateral outline; it is smooth, shghtly narrower
above than below, gently concave from side to side, and roundly convex in
the longitudinal direction with respect to the axis of the shaft. This
surface is shown in figure 6.
The patella is poorly developed in Cynocephalus. It may, or may not,
be completely performed in bone, and there is reason to believe that in
young specimens it will always be found im cartilage or at the best in
yery elementary osseous tissue. When in bone it is not large, though
it extends from a point opposite the center of one condyle to a point
opposite the center of the other, being parallelogramatic in outline, with
the long sides transverse. Anteriorly, the patella is convex from above,
downward, and correspondingly concave posteriorly. The tendon in
which this sesamoid is embedded, the quadriceps extensor, is very tough
and strong and is inserted on the free anterior border of the head of the
tibia.
The tibia is the longest bone in the skeleton of this animal; it is,
however, by no means the stoutest, being exceeded in this respect by both
the humerus and the femur. Proximally the tibia has a shaft the caliber
of which about equals that of the femoral shaft at the junction of its
upper and middle thirds, but as we pass to the distal end this caliber
gradually diminishes until just before arriving at the lower end of the
Yr
198 SHUFELDT.
bone. The shaft, likewise, exhibits a curvature from one extremity to
the other, the greatest amount being at its middle; the entire convexity
is on the outer side. The shaft of the tibia in most mammals is triangular
in section, but in Cynocephalus it is quite quadrilateral, especially where
its caliber is at its minimum. A shallow longitudinal groove marks its
outer aspect, being best seen along the middle third; otherwise the bone,
or rather its continuity, is devoid of any particular characters.
The proximal end, or what is known as the head of the bone, is expanded
and nearly as big as the distal end of the femur. This expansion gives
rise to two lateral eminences, the tuberosities of the tibia. They support
superiorly the two smooth concavities with which the condyles of the
femur articulate im life. In extent they are of about equal size, and
between them toward the back of the bone is a low, pointed process, the
spinous process of the tibia. A slight notch occurs in the posterior border
bounding the tibial head which has received the name of the popliteal
notch, and to it the posterior crucial ligament is attached. On the outer
side of the head there occurs a flat, subcireular, articular facet intended
for the head of the fibula. It is of no great size. Posteriorly, the
boundary of the head somewhat overhangs or extends beyond the shaft,
which is here broad, flat, and smooth.
The enlarged distal end of the tibia is not more than one-half the
bulk of the proximal extremity, and it has a form to fulfill a variety of
purposes. Chief among these are its articulation with one of the bones
of the metacarpus, its articulation with the fibula, for the passage of
tendons of certain muscles, and for ligamentous attachment. At its
inner side it is prolonged distally into a prominent process which is the
internal malleolus. Just above this there is a deep, oblique groove, its
lower opening being in front. In life this groove gives passage to the
tendons of the flexer longus digitorum and the tibialis posticus muscles.
There is a small, rough, inconspicuous facet on the outer side of this distal
end of the bone with which the lower end of the fibula articulates. The
extreme inferior surface of this extremity is given over entirely to a
broad, spindle-shaped, articulate concavity which in life articulates with
the astragalus; internally this is carried slightly up the shaft, or at least
upon the back of this end of the bone. In front this extremity is
conyex from side to side and very smooth; over it in life glide the extensor
tendons.
The fibula is very nearly as long as the tibia, being exceeded only by
the internal malleolus of the latter. On the whole it is the most slender
long-bone in the skeleton and, for its length, the straightest. Some
specimens have the proximal moiety reduced to extreme slenderness
while the head of the bone at that end, which makes a feeble articulation
with the tibia, is always reduced to a mere semiellipsoidal nib, only a
few millimeters long, flattened on its inner articular aspect, and convex
SHUFELDT : SKELETON IN THE FLYING LEMURS. ] [PHin. JourN. Scr., Vou. VI, No. 4.
PLATE Ill.
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THE SKELETON IN THE FLYING LEMURS. 199
on its outer. The shaft is smooth, compressed from within, outward,
and very gradually increases in caliber toward its malleolar extremity. In
one specimen (38) this bone is deeply and longitudinally grooved for
the entire upper one-third of its tibial aspect.
Bulbous in shape, its distal end forms the external malleolus, being
obliquely truncate from above, downward, and outward; the inner surface
is given over to the facets for articulation with the tibia and the astragalus
of the foot. Above this is a distinct little process for ligamentous attach-
ment. There is another, but larger, tubercle on its outer aspect. Liga-
ments of the ankle are also attached at a few other points; in fact, the
most important function of this bone in Cynocephalus is to assist in
completing this very essential joint.
Pes contains the same number of metatarsals as manus contains meta-
carpals, and the toes the same number of phalanges as we find in the
hand; that is, three joints in all the toes with but two in hallux.
The study of the foot of Cynocephalus is wonderfully interesting.
Owing to the unusual way the member has been used and ontogenetically
evolved, it has the appearance, on first sight, of having been dislocated.
The articulatory part of the astragalus which articulates with the tibia,
and to some extent the bone itself, has rotated inward and to a degree
forward, so that the longitudinal axis of this long and narrow foot makes
a varying angle with the continuity of the shafts of the bones of the leg.
This angle in the vertical plane may range all the way from 120° through
a right angle to an acut@ one of 70°, according to the manner in which
the animal holds its foot. The member possesses also a certain amount
of motion either backward and forward, when the limb is held away
from the body, or inward and outward, when it is brought near the latter
and the effort is made to move the foot in those directions.
Flower *° states, and it is true, that “The bones of the tarsus of mam-
mals present fewer diversities of number and arrangement than those of
the carpus.” Cynocephalus offers no exception to this rule.
There are seven bones in the tarsus of the colugo, namely the astragalus,
the os calcis or caleaneum, the scaphoid or navicular, the three cuneiforms
(internal, middle, and external), and the cuboid. This enumeration does
not take into consideration the presence of several important sesamoids
which will be noticed farther on.
The astragalus of all the tarsal bones is next in size to the os calcis,
the latter being the largest bone of the foot. In man this bone receives
* Osteology of the Mammalia, 340. Many works have been ‘examined in this
connection, and the literature of the subject is very extensive, but it would
appear that no author as yet has produced sufficient evidence to warrant any
radical change in the nomenclature of the tarsal bones, or to set aside their
homologies as they have long been given in standard treatises on anatomy.
104558——-3
200 SHUFELDT.
the weight of the body in standing and walking, transmitted to it from
the tibia, and to a very slight degree the fibula. Quadrupeds have this
weight variously divided, while in Cynocephalus it appears that this tibio-
tarsal joint sees its chief use as an enarthrodial articulation. Usually the
yery irregularly-shaped astragalus is described as having a head, a neck,
and a body, and such divisions are easily made out. When duly arti-
culated, the head projects to the front in line with the scaphoid, the
cuneiform bones, and the first and second toes. Anteriorly the head has a
large, smooth, convex facet which articulates with a concavity in the
scaphoid and a surface on the antero-superior aspect of the os calcis.**
The latter encroaches upon the surface of the neck beneath. The neck
is somewhat compressed from above downward (here really from side to
side), and is wider in the opposite direction. The entire upper part of
the body is occupied by an elegant, smooth, convex facet for articulation
with the two bones of the leg. This articular surface is carried over upon
the sides of the astragalus, and here the malleoli of the aforesaid bones
articulate, as is the case with nearly allmammals. Fibula gets the smaller
share, a little less than one-half of this articulation. Posteriorly and
beneath we note a well-marked groove, which in life gives passage to the
tendon of the flexor longus hallucis muscle. On the sides there are pits
for the attachment of ligaments. At the center of the bone, on the side
next to the os calcis in articulation, there is an irregular concavity ; this
is on the neck, while posterior to it on the body there is an elliptical
facet for a similar one on the caleaneum. No Muscle either arises from,
or is inserted upon, the astragalus, and as pointed out above the astragalus
articulates with four bones: tibia, fibula, caleaneum, and scaphoid.
The os ealcis or caleaneum, is longer, narrower, and larger than the
astragalus ; the latter projects just a trifle more to the front, while the
former exceeds it in length behind. Altogether the bone is very irregular
in form and has the tendons of a number of muscles and ligaments
attached to it, or arising from it. Os calcis is the tarsal that forms the
skeletal part of the heel and here we find this posterior extension to be
a distinct semi-ellipsoidal projection, subyertically placed upon the body of
the bone. ‘This is generally called its tuberosity, and upon it is inserted
the tendo Achillis. Beyond it, the body of the bone is somewhat con-
stricted and compressed from side to side. Mesially, it throws out a
conspicuous triangular process, the upper side of which articulates with
the under side of the neck of the astragalus. A similar, rather smaller,
*In assigning directions, and the directions in which surfaces look or face,
for the sake of convenience, it is assumed that the animal stands on the ground
as do ordinary quadrupeds, otherwise it would be very difficult to appreciate
the relations of the tarsus to the rest of the skeleton, and the most unusual posi-
tion in which the foot is held with respect to the surface upon which the animal
is traveling.
THE SKELETON IN THE FLYING LEMURS. 201
apophysis, occurs on the outer aspect of the bone just posterior to the
cuboidal articulation ; this is intended for muscular insertion.
Anteriorly, the face of the os calcis is entirely given over to a concayo-
conyex articular facet for the cuboid, which presents a peculiarity, in
that it is conically hollowed on the planter border; into this fits a
pea-like articular process on the cuboid. On the under, or planter, side
of this the two bones are firmly lashed together by a broad tough liga-
ment. There would appear to be some special cause for the development
of a joint such as this, but the cause is not apparent. Internal to the
cuboid articulation there is a small facet for the scaphoid. When the
two tarsal bones thus far described are articulated, and we view them
from what is really the outer side, we note that the plantar aspect of
the neck of the astragalus is oblique and arches over a similar groove
on the caleaneum, the two forming a foraminal passage through which
we can look. Jn the recent state this is filled up by the calcaneo-
astragaloid interosseous Ligament, and is present in nearly all ordinary
mammals. y
The cuboid in Cynocephalus is really more or less cuboidal in form;
its posterior articular face has already been described. It is also articular
in front where its slightly concave surface is divided by a ridge into two,
for the fourth and fifth metatarsals. There is a strong oblique groove
on its plantar surface, and this lodges the tendon of the peroneus
longus muscle. On its mesial aspect the cuboid makes an extensive
articulation with the scaphoid, and also the external cuneiform. Thus
it articulates with four bones: caleaneum, scaphoid, and the fourth and
fifth metatarsals.
Os naviculare, or scaphoid, is rather larger than the cuboid and its
posterior articulation is somewhat remarkable, for it not only articulates
with the head of the astragalus, but on its plantar aspect on the margin
of this articulation, it sends back a distinct process the side of which
articulates with the os calcis, and upon which the plantar surface of
a part of the head of the astragalus rests. This process has a notch
on its outer side. Anteriorly; it has facets to articulate with the three
cuneiform bones. These are all more or less cuboidal in form, differ-
- ing a little in the matter of size, and each articulates anteriorly with
the base of a metatarsal. The internal cuneiform is the largest and
joins the hallux metatarsal; it extends farthest to the front; the middle
one is the smallest, and the external one is between the two in point of size.
The three middle metatarsals very closely resemble the correspond-
ing bones in the hand, while in the foot a peculiarity is seen in hallux
metatarsal in that it has a conspicuous, rounded process erected on the
dorsal aspect of its extreme distal end. The articular surface in front
is carried upon this, affording the joint next beyond an unusual amount
of backward play in the vertical plane.
202 SHUFELDT.
The metatarsal of the little toe is almost as stout as, and considerably
longer than, hallux metatarsal, and as in many other mammals it deve-
lopes a process proximad that projects from the side of the foot. This
is the tuberosity of the fifth metatarsal; in man and probably in many
other mammals the peroneus brevis muscle is attached to it.
The distal phalanges as well as the greatly compressed ungual joints,
closely resemble those of manus and consequently require no special
description.
At the side of the foot,.a short distance back of the hallux meta-
tarsal and apparently encased in the lateral ligaments in that locality,
there is a large, flat, quadrilateral sesamoid. It is on the tibial side of
the tarsus and rests, flatwise, on the scaphoid and internal cuneiform
bones. Baur took this to be the rudimentary tarsale tibiale in which
he was doubtless mistaken, as it is sesamoidal in all its characters.**
Tt would appear that no special name has as yet been bestowed upon
this bone, so it might conveniently be known as the tarsal sesamoid.
There are other sesamoids in the sole of this foot, and they agree in all
particulars with the corresponding ones in the hand. We see them,
proximad, just within the tarsophalangeal articulations, a pair back of
each jomt, and very much smaller pairs in the row of joints beyond.
Occasionally specimens are found having a few very small sesamoids in
the sole of pes, and in the partly cleaned skeleton the palmar surface of
the process projecting backward from the scaphoid may easily be mistaken
for one, as it is exposed there and has the same elliptical form.
No tendon of any of the muscles in Cynocephalus has been found to
ossify, nor have there been, beyond the rings of the trachea, any other
ossifications met with in this animal.
So much then for the osteolgy of Cynocephalus, the caguan, the
aberrant insectivore of certain islands of the Indian Archipelago, which
we know is certainly no lemur.
THE HYOID ARCHES AND THE LARYNX.
As stated above the specimens here described lacked the hyoid arches
and the trachea. ‘This I communicated to Mr. McGregor by letter and
in due time received the following reply from him. ;
I have, unanswered, your letters of October last and of January of this year
[1909.] I am glad to know that you have a paper on Galeopithecus roughed
out and I will hope to-be on hand to see it copied and to read the proof for it.
I regret that the specimens sent you were incomplete. They were prepared in
the field by my assistant at a time when we had a great press of other work
and you know what that is in a hot climate. I am fortunate in having on
hand a pickled specimen of the lemur from Basilan, doubtless the same species
2 Amer. Nat. (1885), 19, 349. This bone has also been discovered to exist
in Hyraz, the duckbill, certain Rodentia, and in some of the Edentates.
THE SKELETON IN THE FLYING LEMURS. 203
as the Bohol specimen, and I will forward the entire head and neck of this in hope
that you may be able to dig out the hyoid from it. It has been long in formalin
so that the bones may have softened a bit or perhaps hopelessly so, at any rate
I think it worth while to forward in case it will complete your description.
If you have already mailed your manuscript you can write out the hyoid
matter and send to me with indication where to insert, ete., and I will see that
it is properly placed in your manuscript.
Toward the latter part of April, 1909, I received by mail the above
mentioned head and found it to be a specimen of the kind described by
Mr. McGregor and in a very satisfactory condition for dissection. I
have carefully dissected the hyoidean apparatus, the larynx, and about
an inch of the trachea (all that came with it) of this specimen.
I have compared all the parts with the corresponding ones of a domestic
cat as figured by Mivart, and with several other species of the Carnivora,
bats, ete. Upon the whole it agrees pretty well with the first-named
animal, except in the matter of the tympanohyal, and it was Flower °°
who said:
The hyoid [in the Insectivora] is formed generally like that of the Carnivora,
with three complete extracranial ossifications in the anterior arch, a tranversely
extended basihyal, and tolerably long, stout, flattened thyrohyals, sometimes anky-
losed with the basihyal.
The tympanohyal in Cynocephalus, if it exists at all, is very small and
codssifies with certain bones at the base of the skull between the periotic
and tympanic elements in the neighborhood of the stylomastoid foramen.
Neither Dobson nor Flower, I believe, ever described the hyoid or the
ossifications of Cynocephalus, and in fact up to the present time I have
not met with any observations of any kind upon this part of the skeleton
of the flying lemur.
The specimen at hand is from a fully adult animal and probably
ossification in the parts has gone as far as it ever goes in this species,
though in individuals attaining an unusual age it may be carried some-
what further.
The anterior cornu has a length of 1.5 centimeters, and the posterior
cornu has a length of 6 millimeters, while the average height of the laryn-
geal box is 7 millimeters, and its width about the same, the former in-
cluding the crinoid cartilage.
So much of the windpipe as remained with this specimen is composed
of vertically narrow, closely adjusted rings. These rings are not large;
they are transversely elliptical, performed in elementary bone, and while
thinner posteriorly they appear to unite in bone in the medio-vertical
line; the first few superior rings certainly do. All the parts usually
found in the larynx among the higher vertebrates are present, but it is
only in the case of the anterior thyroid ale that firm ossification is
2 Osteology of the Mammalia, 176.
204 SHUFELDT.
observed ; all the other elements remain in cartilage and these, apart from
the cricoid, fuse more or less together.
The hyoidean apparatus rests directly upon the top of the larynx
and it is only the limbs of the anterior cornua, including the epihyals
and stylohyals, that stand out independently; these project posteriorly.
Hach thyrohyal is broadly paddle-shaped,.the blade being in front and
directly articulating on either side with basihyal. They only connect
with the superior cornu of the thyroid by means of cartilaginous ex-
tensions. Parallelogramic in outline, the basihyal is nearly flat, being
but very slightly concave from side to side posteriorly, and correspond-
ingly convex in the same direction in front. The stylohyals are entirely
in cartilage and rudimentary, while both the epihyals and ceratohyals
are in hone, each being represented by extremely delicate little rods,
making feeble articulations with each other upon either side, and with
the basihyal anteriorly.
It will be of interest to mention, incidently, that Cynocephalus has a
very large thick tongue, finely serrated on the thin edge of its semi-
circular, anterior margin. The roof of the mouth is peculiarly cor-
rugated in curious, transverse, zigzag lines, and these being raised leave
strong similar impressions on the sttperior surface of the tongue. This
last may be of a post-mortem nature and may not exist during life.
NOTES ON THE OSTEOLOGICAL MATERIAL REPRESENTING THE GALEOPTE-
RIDZ IN THE, COLLECTIONS OF THE UNITED STATES NATIONAL
MUSEUM. THe”
After the typewritten copy of this memoir had been forwarded to me
by Mr. McGregor for revision and had received my careful reading, it
occurred to me that the value of the memoir would be greatly enhanced
if certain parts of it were read by such an eminent writer on mammalogy
as Mr. Gerrit S. Miller, jr., curator of the division of mammals in
the United States National Museum. Mr. Miller at the time was im
Hurope, and did not return to Washington until the early part of Sep-
tember, 1910. On the first of the followimg month I took the material
I had deseribed, together with the typewritten manuscript to Mr. Miller
at the Museum! and after taking up some of the points in the latter, he
advised me to make a thorough comparison of the skeletons and skulls
of my own collection with those of the far more extensive collection
of the Galeopteride belonging to the United States National Museum,
together with a series of skulls of flymg lemurs loaned him by the
Bureau of Science. Mr. Miller informed me that all the species of these
animals belonging to the Malayan fauna were now contained in the
genus Galeopterus, and that the Philippine species volans was of the
genus Cynocephalus.
There are a number of Malayan species and perhaps subspecies, but
THE SKELETON IN THE FLYING LEMURS. 205
the skins and osteological material of the Philippine forms were as yet
not sufficiently extensive in the National Museum collections to differ-
entiate them. In addition to the above-mentioned material, Mr. Miller
placed at my disposal a particularly fine and perfect mounted skeleton
of an unidentified Malayan form of flyimg lemur belonging to the
National Museum. This specimen was photographed for me by Profes-
sor T. W. Smillie, chief of the photographic division of the National
Museum, and the reproduction of this photograph illustrates the present
memoir as a frontispiece. It is particularly valuable as showing the
skeleton in one of these animals with all the bones, even including the
hyoid and trachea, normally articulated. There is listed in the following
tables all of the osteological material (October 1, 1910) representing
the flying lemurs in the collection of the United States National Museum,
which I have compared and studied. The scientific name given is the
name on the label attached to the specimen. Such information likewise
applies to the locality, sex, and name of collector given. In some in-
stances the condition of the specimen is added.
Skulls of Cynocephalus from the Philippine Islands, United States National
Museum collection.
7 7
nies cue Name. | Locality. | Sex, age, ete. Collector.
i —!- —— — | ——— — oe ee — —— ~
144663 | 6145 | Cyanocephalus | Catagun, Min-| Adult ¢; broken, | E. A. Mearns.
volans. danao. inc. plete.
144662 GO46)| Ben dole se ee Basilan Island Isa- | Adult ¢__----______ Do.
bela. |
144660 6036 |----- (oh) ae eee CS es eee -|-----do_____--------- Do.
144659 6034 }----— (6 Koes ee as (OS Do.
25499) | eee coh: Pantar, Mindanao__| Not given; adult, | Not given.
| perfect.
144655 6027 | Cyanocephalus | Basilan Island, Isa- | Adult 2 BR. A. Mearns.
| volans. | bela. |
144657) 6030. do = [Bett cymes ames 8 Broken up; adultg_) 5. A. Mearns,
| | 1906.
144656 60285 | eee Oyeanee a= anes eee do___._--____-_-_/ Adult 9; perfect ____| E. A. Mearns.
144658 CUES |e donee Rie ame ewe! Omens eaiee Sn) ANGI Oe Do.
144661 | 6038 |_____ do. Reena ee Near o Hulree Ou BL Juvenile Q____---___ eae:
| |
Skulls of Cynocephalus from the Philippine Islands, Bureau of Science collection.
|
Original | Locality. | Sex, age,ete. | Collector.
number. | Namie:
105 LAGI (ofan a | R. C. McGregor.
111 | Not given Do. |
108 | Adult 9__ | Do.
104 ANGKPNNG pote e | Do.
flO Gy] ered pee re een eae eee] yaaa AN fa |e ove esnneiaaks | Do.
Two skeletons of Malayan species.
\U.S. Nat.
SHUFELDT.
United States National Museum.
| Mus. Name. Locality. Sex, ete. Collector. *
| number. | |
ieee need CIEE Nee Wet TG | iat
49640 | Galeoplerus sp.2 | Pulo, Bintang | AGU teO soe | (2) t
| 154600 |-_-_= (s\oyeas Ronere er | MountSalak, Tandak _ Juvenile, complete_| O. Bryant, 1909,
| Java Expn.
Skulls of Malayan species, United States National Musewm.
1S a | oa | } |
Y Mus. ee Name. | Locality. Sex, age, etc. | Collector.
| 122841 | 2454 | Guleopithecus —___- | Malacca Strait, ©) sty . Nostril between nasal and internasal, which are completely fused in
front of the nostril. Light yellowish-brown above, with 4 dark
brown, longitudinal streaks, the middle ones broader than the
lateral; whitish-yellow below ...... .. Ablabes philippinus Boettger.
Culion and Samar (Boettger); Iwahig, Palawan (Bureau of
Science collection). Found only in the Philippines.
ec. Anterior temporals absent, the parietals being in contact with the
labials; nostril in a single minute nasal; no loreal. Very small
snakes.
da‘. Internasals present Genus Pseudorhabdium.
e. Supraocular distinct; a preocular; frontal longer than broad.
Iridescent brown, often with a yellowish collar.
Pseudorhabdium longiceps (Cantor).
Daraga, Luzon (Peters). Found also in the Malay Peninsula,
Sumatra, Borneo, and Celebes.
262 GRIFFIN.
e*, Supraocular very small and united with the postocular; no
preocular; frontal broader than long. Uniform iridescent dark
DIOWN. eso Pseudorhabdium oxycephalum (Giinther).
Negros (Boulenger). Found only in the Philippines.
@SiNowmternasalls; se ke Se ee eh ee Genus Calamaria.
e*. Symphysial in contact with the anterior chin-shields.
. Frontal less than twice as broad as the supraocular. Black
above, barred with alternate bands of black and white below.
Calamaria grayi Giinther.
Recorded by Giinther as from the “Philippines,” the definite
locality being unknown. Not known elsewhere.
-. Frontal at least twice as broad as the supraocular. Rostral as
deep as broad, frontal as long as the parietals. Brown above,
uniform yellowish below ..........-..--.- Calamaria bitorques Peters.
Luzon (Boulenger). Restricted to the Philippines.
. Rostral as deep as broad; frontal shorter than the parietals.
Brown above, with several fine light streaks on each side,
yellow below (in spirit, white) .
Calamaria gervaisii Duméril et Bibron.
Manila (Jan); Batu, Daraga, Paracale, Mount Iraga
(Peters); Bataan (F. Miiller) ; southern Negros (Giinther) ;
southern Mindanao (J. G. Fischer) ; Manila (Bureau of Science
collection). A purely Philippine form.
f*. Rostral broader than deep; frontal shorter than the parietals.
Brown above with longitudinal series of black dots; a yellow
spot on each side of the neck.
Calamaria mindorensis Boulenger.
Mindoro (Boulenger). Only the type specimen is recorded.
é. Symphysial not in contact with anterior chin-shields.
f'. Diameter of eye much more than its distance from the mouth.
Brown above, with two longitudinal rows of dark spots on
@aChy Side ectee fee a eee eee Calamaria everetti Boulenger.
Palawan, (Boulenger) ; Iwahig, Palawan (Bureau of Science
collection). Also found in Borneo.
f. Diameter of eye less than half its distance from the mouth: 250
ventrals. Dark brown above, with the two outer scale rows
tipped with yellowish; a yellow collar on the neck; a pair of
large pale lateral spots at the base of the tail.
Calamaria mearnsi Stejneger.
Mindanao (Stejneger). Only the type specimen recorded.
d°, Internasals present; eye concealed under the ocular shield. Uniform
blackish, scales edged with white. A Philippine genus with a
single species -..-.-....------------ Typhlogeophis brevis Giinther.
Northern Mindanao or Dinagat (Giinther): Only the type
specimen known.
7h
~
ors)
Series B. Opisthoglypha.
One or more of the posterior maxillary teeth grooved and usually enlarged,
forming small fangs. The snakes of this series are poisonous, but on account of
the position of the fangs in the back of the jaw and their small size, they are not
often dangerous to man. Their prey consists principally of lizards and small
mammals which they paralize before swallowing.
CHECK-LIST AND KEY OF PHILIPPINE SNAKES, 263
@. Nostrils valvular, on the upper surface of the snout; aquatic snakes.
Subfamily Homalopsine.
b+. Nasals in contact. Scales keeled; numerous small scales in place of the
JOUER IS), ete tee aaa re pe ee oer ee ea ase Genus Hurria.
ce. Four lower labials in contact with the anterior chin-shields; scales strongly
keeled, in 23 to 27 rows, ventrals 132 to 160. Light brown above and
below, spotted and barred with dark brown.
Hurria rhynchops (Schneider).
Manila (Jan); Batu, Daraga, and Buhi, Luzon (Peters); Negros
(Ginther) ; Placer, Mindanao (Giinther); Palawan (Boulenger) ; Ban-
tayan, Polillo, Palawan, Cuyo (Bureaw of Science collection). Found
along the coasts of India, Ceylon, the Malay Peninsula and Archipelago,
the Pelew Islands, Timor, and the Moluccas.
@, Three lower labials in contact with the anterior chin-shields; scales fully
keeled, in 29 rows; ventrals 163 to 165. Color about the same as in
Hurria rhynchops (Schneider) ...............- Hurria microlepis (Boulenger).
Philippines (Boulenger) ; Camiguin (Bureau of Science collection).
Not recorded from any other locality.
b?. Nasals separated by a single internasal. Dark olive or gray above, with
.a broad white band on each side.
Gerardia prevostiana (Hydoux et Gervaise. )
Manila (Duméril and Bibron). Found along the coasts of India, Ceylon,
and Burma.
a, Nostrils not valvular, lateral; mostly tree or bush snakes.
Subfamily Boigine.
6*. Anterior mandibular teeth strongly enlarged; scales without pits; sub-
caudals single; pupil round; scales smooth; solid maxillary teeth equal,
20. Hypapophyses developed to some extent throughout the vertebral
column. Brown above, with black spots on the head and neck, and a black
line on each side of the posterior part of the body and the tail; lower
partsieyellowasht ees e Set coer csceseseeecreceee Hologerrum philippinum Giinther.
Philippines (Boulenger). A genus containing only a single species, and
limited to the Philippines.
b?. Solid maxillary teeth subequal; head very distinct from neck, pupil vertical.
Genus Boiga.
ce’. Anterior palatine teeth but slightly enlarged.
@. Snout longer than the diameter of the eye; scales in 21 rows. Ringed
by alternating, broad black and narrow yellow, bars.
Boiga dendrophila (Boie).
Samar (Peters) ; Mindanao (Giinther) ; southern Mindanao (J. G.
Fischer); Palawan and Mindanao (Boulenger); Palawan, Rizal
Province, Polillo (Bureau of Science collection). Found throughout
the Malay Peninsula and Archipelago.
d’, Snout as long as the eye; scales in 19 rows. Grayish or yellowish brown,
with dark brown spots and cross bars, the latter extending across the
[ae aa ean ee ee Boiga angulata (Peters).
Leyte (Peters) ; Polillo (Bureau of Science collection). i ° y Sy .
pc MI as PASO Ne
.
¢ CREST) alias
' ; s ‘7 seed Pe ee
1 a oe
n j o.
. . <
a x
) ;
~ ° ‘
—
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; Spores ech i,
‘
ve REVIEWS.
.The First Grammar of the Language Spoken by the Bontoc Igorot with a Voca-
bulary and Texts, etc. By Dr. Carl Wilhelm Seidenadel. Price $5. Chicago.
The Open Court Publishing Company, 1909. (Date of publication: April
1910.)
This grammar of a hitherto unexplored dialect spoken far up in the
mountain fastnesses of northern Luzon can not but have come as a sur-
prise to persons resident in the Philippine Islands and interested in the
study of the vernaculars of their peoples since it originated on the op-
posite side of the globe, at Chicago, in the heart of the United States
of America. The explanation is, perhaps, in more than one sense,
characteristic of the new order of things.
The bulk of hitherto existing grammars and vocabularies on Philip-
pine languages is made up of more or less time-honored works written
by Spanish friars to whom the study of these languages was of immediate
practical interest. It is characteristic of these works, especially of the
older “Artes y Bocabularios,” products of years of linguistic study and
practice among the natives, that they existed often for a considerable
time only in manuscript form, and thus were copied and passed on from
colleague to colleague and from one generation of missionaries to another,
until, after many corrections and additions, they ultimately appeared in
print in Manila.
Here, now, we have the work of an American philologist, Dr. Wilhelm
Seidenadel, who, withoutleaving Chicago, his place of residence, has been
in contact for not more than about six months (two and one-half months
in 1906, and three and one-half months in 1907) with two successive
groups of Bontok people, who, from their mountain home in far Luzon,
were sent to America for exhibition. Their presence excited in him
a great interest in the strange tongue and he set himself to study it.
“The difficulties seemed at first unsurmountable, for none of those whom the
author met at first understood English sufficiently well to comprehend questions
or to give explanations. Thus it became necessary to force the way into their
idiom by their idiom, but what had appeared, in the beginning, to be almost
a misfortune, proved afterwards to be a blessing: the necessity of using in the
research almost exclusively their vernacular, through which the investigator
succeeded in gaining genuine and correct material, such as in many other Malayo-
Polynesian idioms is collected from unreliable translations of the Bible, from
prayerbooks, manuals for priests, reports of unphilological officials, traders, mis-
sionaries and similar sources. While the material was taken down during the
271
272 REVIEWS.
first few weeks without any definite plan, the fascinating success soon induced
the author to proceed systematically. Henceforth it was his aim to elicit from
the Igérot as many examples as possible, illustrative of grammatical rules already
sketched, and to collect an extensive vocabulary of genuine Bontoc Igérot words.
But, as a matter of no less importance, he never neglected to take down also
from the Ig6rot’s mutual conversation as many phrases as he could obtain,
although the significance of most of them was quite obscure, at that first period
of his research.”
I take these quotations from the author’s narration of the genesis of
his work as given by him in the preface. To judge by the date of the
latter, the writing of the grammar was finished by October 18, 1907,
that is, two months after the departure of the last group of Bontok people
from Chicago. This is indeed a remarkable achievement of rare lin-
guistic talent combining enthusiasm and perseverance in a self-imposed
scientific task. The magnificent volume in which the labors of the author
have found their embodiment may truly be regarded as a monument
erected to these qualities by that group of American citizens who through
their munificence made possible the publication of this work.
The main parts of the book are:
A collection of photographs showing, in various attitudes, individuals and
groups of those representatives of the Bontok people who went to Chicago on
exhibition.
An inscription to the patrons alluded to above.
Preface (pp. VII-xv).
List of contents (pp. XVII—XXIV).
Part I: Grammar, with appendix on Bontok proper names (pp. 1-270).
Part Il: Vocabulary, with preface (pp. 273-475).
Part III: Texts, with preface including a section “To the memory of Matyu
from Bontoe” (Detroit, Michigan, September 3, 1908) (pp. 479-583).
Addenda et Corrigenda (pp. 587-588) .
In connection with the epitaph just mentioned, I may dwell here on a
feature of Doctor Seidenadel’s work which impresses us in different parts
of the book. It is his profound humane sympathy with his Bontoe
friends, a sympathy which, transcending the mere professional interest
taken by a scientist in the object of his study, would seem to be—accord-
ing to the dictum: “Alles Verstindnis kommt uns nur durch die
Liebe’—a guarantee of the faithfulness with which he has interpreted
in his grammar genuine Bontok thought and speech.
THE PREFACE.
The preface, as has already been indicated, makes us acquainted
with the peculiar cireumstances under which the book was conceived and
born. After a review of the literature already existing on Bontok the
author proceeds to give us an insight into the purpose and plan that
guided, him in writing his grammar. To explain the absence in it of
all comparative studies, he states that he considered it his task
REVIEWS. BUS
“to furnish material for such studies, to contribute at least a certain amount
of reliable material for comparative research, which ought to be based upon the
results of new, uninfluenced investigations—fieldwork—into the various idioms as
spoken by the natives, and not upon religious books made by missionaries and
their apprentices. It were best to consider the entire field of Philippine languages
as yet untouched and to begin anew to study (but not without personal sympathy
with the natives!) ‘jene Prachtwerke des malaiischen Baustils, die philippinischen
?
Sprachen, ..... * Concerning the plan underlying the grammar we are told:
“While composing the grammar, several methods of arranging the material sug-
gested themselves. The Author concluded—indeed not without hesitation—that
it would be more convenient for students trained in the grammars of Indogermanic
Languages, if he would retain, with slight modifications, the customary order
of the chapters in such grammars, if he would first treat the articles, then the
noun, pronoun, adjective, ete., just as if the Bontoc Language would distinguish
the same grammatical categories as the Indogermanic Languages. This method
seemed helpful for acquiring knowledge of the idiom, but for practise the student
must absolutely abandon those former conceptions of etymology and syntax which
he may have gained from his previous studies of the classical or modern Germanic
or Romance Languages; the sooner he can free himself completely from clinging
to his former notions of the structure of a language and adapt himself to new
categories of linguistic elements, the earlier he will succeed in entering into the
spirit of this admirable idiom.”
It appears herefrom that, while the book is primarily intended to fur-
nish material for studies in comparative Indonesian philology, that mate-
rial is presented in such a form that it is available also for those familiar
only with grammars of Indogermanic languages. The grammar is thus
both critical and didactic; it investigates and discusses, and it teaches
and is intended to be practiced. The combination of these two tasks
offers, of course, certain difficulties, and where no systematic division is
‘instituted, the claimants of either of the two spheres of interest involved
must have the good grace to make certain concessions to those of the other.
To consider first the interests of “the tradesman, the engineer, the
teacher, the missionary, the official,” who are given directions on page 279
how to derive practical advantage from the book, the reviewer is of the
opinion that they could hardly do better than imitate the splendid
example set by the author himself and use the vernacular from the very
outset in talking with the natives. If, having thus acquired a smattering
of the language, they begin reading the grammar, taking a suitable section
day by day, and consult the book on every point of interest arising, they
will certainly come to feel grateful to the author for his research work,
and will be in a position fully to appreciate its merit.
LIST OF CONTENTS.
Both the practical student and the philologist probably will regret
that the treasure of information stored in this volume has not been made
somewhat easier of access. The List of Contents, as far as it refers to
the grammatical part, might advantageously have been made more synop-
tical by preserving in it the same division into chapters and sections into
274 REVIEWS.
which the text is actually divided. Without the headings used in the
text and reduced to a running enumeration of the 462 paragraphs that
make up the grammar, the List of Contents makes the latter wrongly
appear a mere aggregate of grammatical details, among the great mass
of which any particular matter is not easily detected.
THE GRAMMAR.
The Grammar begins by stating by whom the Bontok language is
spoken, and its territorial extension.
The author then gives a list of the symbols used by him to represent
the sounds of that speech. As we become acquainted with the many
indistinct, fluctuating, and interchanging sounds with which it abounds,
we realize the difficulties the author had to conquer in making his way
through this first barrier and must admire the conscientious and pains-
taking manner in which he has undertaken to present to us throughout
the book the peculiar Igorot sounds according to his system. It is but
a proof of this conscientiousness that he, himself, in the preface calls
attention to some inconsistencies in orthography, accents, and quantity.
We are told that these are but a consequence of the changing elocution of
the natives for whom he did not consider himself entitled to create a
normal language. This is a very sensible remark, and one that touches
at the root of the controversies which arise from time to time over the
proper graphic representation of several sounds occurring in all these
Indonesian languages, written or unwritten. Where the speakers them-
selves, contemporaries in the same town or settlement, are not yet agreed,
one with the other, nor each with himself, as to a definite pronunciation of
their tongue, the exploring linguist would indeed commit a mistake in
covering up the existing unstableness by fixing a normal spelling for
himself. There is one statement in the author’s description of Bontok
Igorot sounds upon which some comment may be useful as it relates to
an apparent divergence of views found among some authors on Indonesian
languages. Under the heading diphthongs, the author states: “All diph-
thongs are vocalic with a final consonantal sound y or w.” Regarding
the class of diphthongs here implied, a similar remark is often met with,
namely, that the second part of the combination contains something con-
sonantal, or is a consonant. ‘To explain this sound the two symbols, y
(in Dutch j) and w, are referred to. It would certainly promote a clearer
understanding if, instead of two ambiguous letters the pronunciation of
which varies with different nationalities, a physiological description of
this consonantal something were given. What is to be understood here
by “consonant”? Is it, in the etymological sense, a sound which, more
or less indistinct to the ear if alone, only sounds together with a vowel?
This would be nothing more than the ordinary character of the second
REVIEWS. 275
part of the diphthongal combination here discussed, so that, once called
diphthongs, it would be understood that the first part of the combination
carries the syllable while the second part is reduced so as to give just a
margin of different vocalic color to the first, remaining, however, vocalic
to the end. 'The reviewer, for his part, has not been able to detect more
than this in the mouth of Filipinos of different tribes whom he has asked
to pronounce those diphthongs, nor can he find it in the examples by
which the author illustrates some of the Bontok Igorot diphthongs:
“ay nearly like ai in aisle
“ey nearly like ey im eye, or ei in height
“oy as in boy.”
But by the term “consonant,” used in the case alluded to, more may
be meant. That term is also defined as denoting, in the precise case here
under discussion, a sound in the production of which that narrowing
between lip and lip, and between tongue and palate, which is necessary for
the articulation of w and 7 respectively is carried to the degree of becom-
ing an obstruction to the passage of the breath, thus producing that rub-
bing sound which is characteristic of the class of consonants involved
(spirants or fricatives) and in which the vocalic element becomes extin-
guished. To this class belongs the sound contained in certain French
words cited by the author to illustrate the following diphthongs:
“oy as in French feuille,
“wy as in French fouille,
“iy as in French tuyau.”
As regards the group “ao, au, as in how” it would seem that as long
as the lips in pronouncing the second part’ of the combination remain
sufficiently open to make a fluctuation between o and w at all noticeable
it is not probable that the narrowing required for the labial spirant is
reached ; neither is it reached in the English word “how” used as example.
After a detailed exposition of Bontok Igorot phonology the author
proceeds to treat consecutively: the Article, Noun, Pronoun, Adjective.
Verb, Numerals, Prepositions, Adverbial Expressions, Particles, Conjunc-
tions, ete. In so doing he amply fulfills his promise in the preface, to
assist the student in all possible ways on each page of the grammar by
establishing rules, by an abundance of examples and by frequent literal
translations not only into English, but, wherever considered more helpful.
into German, French, Spanish, and Latin. As, at the same time, he
dwells upon and explains in their finer shades the turns of Igorot phraseo-
logy, the student, in advancing, also becomes initiated into the spirit and-
rules of syntax, so that, when the last part of speech is reached, there
remain to be considered only a few special syntactical constructions.
Chapters like Modifiers of Verbs (p. 117-130), Auxiliaries Constructed
1067134
276 REVIEWS.
with Ligature ay (p. 130-134), Modifying Verbs (p. 134-138), Negatives
(p. 138-148), which are among the most imteresting of the book, show
clearly how profoundly the author has penetrated the intimacy of Igorot
speech notwithstanding the short time allowed him for its practical study.
The grammar in general convinces us that the material, in the first
place, has been collected with great care and diligence, and afterward
very studiously arranged so as to present it to the student as one
systematic whole.
It is in connection with this latter point, namely, the systematization given
by the author to his matter, that I wish here to take up and extend a little the
remarks made at the beginning on the formation of Philippine grammars in
the past.
Since it has been recognized that every language carries its order in itself,
it is a just demand that this natural methodical disposition of its several parts
be made the basis upon which the structure of any language, or group of closely
related languages, be presented in a grammar. In the older Philippine grammars,
those written by Spanish friars, we find this principle generally not carried out,
either because it had not yet been established clearly and universally at that
time, or because any attempt to evolve a natural system or order was subordinated
to the practical purpose of instructing the younger members of those religious
corporations in a manner then considered most adapted to their previous schooling
in Latin. The fact is that Latin furnished the model for these Indonesian
languages. Latin grammatical categories, by more or less specious interpretation
of the native forms, were also found in Tagalog, Pampanga, Pangasinan, ete.
As far as concerns the interest of the vernaculars, and not that of the students,
the procedure was clearly recognized as improper, at least by some authors.
Thus. P. Francisco Lopez, the excellent Ilocanist, says: “Aunque el idioma de estas
lenguas es muy diferente de el de la lengua Jatina; con todo eso, en cuanto fuere
posible, nos conformarémos con el método de el Arte de Antonio de Nebrija, por
ser 6] por donde los mas de los Religiosos que vienen 4 estas Islas han estudiado
el Jatin. Y asi hallaran mas claridad y facilidad en aprender esta lengua.”*
But the evil produced, the obscuration of the genuine character of these languages,
makes itself felt till to-day, both in the Philippines and outside, and the condemn-
ation in Doctor Seidenadel’s Bontok Grammar of a particular “fallacy”—of which
more presently—merits the more attention as he is a classicist himself. How ill
adapted Latin as a grammatical taskmaster for an Indonesian language really is,
may be gathered from an extract of what may be called a summary of the short-
comings of Austronesian languages if tested upon the presence in them of
grammatical forms characteristic of inflectional languages, as given by Doetor
Codrington in his classical work on the Melanesian languages: “These languages,
all of them, are destitute of inflexions, and this gives them a common character.
There are, therefore. no Declensions or Conjugations: there are no Cases, no
Genders, and, excepting Pronouns, there is no Number or Person. Since, then,
these grammatical forms do not exist, it is unreasonable and undesirable to speak
of them as if existing .... Corresponding with the absence of Inflexion there
is an absence of those variations in the form of words which may distinguish
the Parts of Speech. It is not that there is a complete absence of such speeial
*Gramiatica ilocana, compuesta por el P. Predicador Fr. Francisco Lopez... .
Third edition, Malabon (1895) p. XIII. (First edition 1627.)
REVIEWS. 277
forms as Verb or Noun, but that the same word, without any change of form,
may be in use as almost any of the parts of Speech. The use of the word, not its
form, commonly declares its character .... - 5
The first among Spanish grammarians to depart from the traditional Latin
observance was probably P. Toribio Minguella. For the use of other than Latin-
bred students he published in 1878 a Tagalog grammar which, perhaps on account
of its being an attempt in a new direction, he modestly called “Ensayo de
gramatica hispano-tagala.” In this work-he endeavors to do more justice to the
language itself. Besides fitting the grammar for practical use by giving exercises
and matter for reading and translating, he guides himself, in presenting the
structure of the language, more by its own forms, and introduces certain terms
denoting grammatical categories under discussion of their definition and their
applicability to Tagalog.
As was seen in a previous quotation from Doctor Seidenadel’s preface, the
proper arrangement of his material has been with him likewise a matter of
consideration. Consulting in this respect the convenience of students trained in
Indogermanic languages, he decided to adhere, with slight modifications, to the
customary order observed in those grammars, designating that order, however,
as one applied to his grammar only “as if the Bontoc language would distinguish
the same-grammatical categories as the Indogermanic languages.” We are, then,
not at liberty to look upon the order followed by the author as representing his
views on the proper systematic presentation of an Indonesian language such as
Bontoe Igorot; but we are also absolved for. the same reason, from giving
consideration to that hypothetical plan from this point of view.
Still, as already indicated above, at one point of his chosen plan the author
makes a strong criticism of the views held by a number of Indonesian philologists
concerning certain classes of derivatives particularly characteristic of Philippine
languages, and since the reviewer is completely in accord with the negative part
of the author’s contention, and believes that the time has come for a revision of
prevailing views involved, he extracts here some of the paragraphs in Doctor
Seidenadel’s grammar which bear directly on the matter.
212. If roots shall be formed into Nomina actionis, they receive (after certain
phonetic changes [220]) one of these verbalizing particles:
I. the suffix -en (but no prefix)
Ii. The suffix -an (but no prefix)
Il]. the prefix 7- (but no suffix)
213. By combination with one of these particles the root is transformed into an
Active Verbal Noun. The particles indicate that the action named by
the root passes from the agent to an object. They give the Active
Verbal Noun transitive force.
216. Since the Nomen Actionis possesses active foree—as has become evident
through many various experiments with the spoken language—the
relations of the direct object or accusative, in our conception, to the
Nomen Actionis with -en is: (a) Hither the object of the Nom. act. is
in the accusative; it is governed by the Nom. Act. which has its
transitive force in the suflix -en. If we represent this transitive force of
*The Melanesian Languages by R. H. Codrington, D. D. Oxford 1855, pp.
101-102. The judgment quoted may appear somewhat severe; as a remedy against
the belief in the universality of Latin categories, it is certainly wholesome.
278 REVIEWS.
-en by our verbs “‘to affect,” or “to concern” or “to influence,” we obtain
this translation:
leytjenmi tjaitja: our liking concerns them.’ (b) Or the object is in
the predicative nominative; the transitive force of -en may be indicated
by words like “aim,” “object”:
alaentako nan tolfeg: our taking-object (is): the key
217. The relation of the object to the Nomen actionis with suffix -av is analogous
to the construction mentioned in [216], if we assume the possibility
that -an is probably identical with -aen, or merely a variation of -en, in
this combination with Nom. actionis. The following theory seems to
be more plausible: -an is the locative particle, as affixed to substantives
in [56-58]. The object is the place where the action named by the
Active Nom. act. “takes place”, to which it tends; it is the end of the
action. We can translate:
ayakantako nan aliwidtako our calling-end (is): the man *
218. The relation of the object to Nomina actionis with the prefix 7- appears
to be the same as that to Nom. Act. with -en; i- performs here a similar
function as -en does there; 7- directs the action towards the aim, the
object.
(I- may be compared with our prefix be- in bespeak, befall: or it may
represent the preposition is, and may then be compared with invade,
offend, persuade, provide, and other prepositional compounds. )
In certain cases i- points to a person in whose behalf another acts, and
to the tool which a person uses in performing or executing that which
the Nom. act. names;
itafongko nan soklongna my hiding affects his hat. The discussion of
the constructions in the examples of -en, -an, i- Verbs given [216-218]
was attempted for the purpose of facilitating translation and re-
translation and with the assumption that there were in Bontoe Igérot
eases of the substantive, distinctions between nominative and accusative,
which do, in fact, no exist: the Bontoe Igérot does not distinguish
between Casus rectus and obliquus.
Later, on page 95, the author returns incidentally to the subject under the
heading Future Passive:
The imperative [of the Passive] does not exist: any theoretical forms and
any experimentative use of them in sentences were unexceptionally denied;
“Because you cannot tell a man what shall be done to him”... (But the
misnamed “Three Passives” (the “Genus Relativum’, my Active ‘“Possessive
Verbs”) were put in the Imperative without hesitation; this shows also that the
-en, -an, i- verbs are conceived to be Active Nomina Agentis.)°
To the parenthetical clause of paragraph 218 above quoted the following is
added as a footnote:
. However convenient for minds trained, to some extent, in Latin, the Doctrine of
the Three Passives has appeared, centuries ago, to its inventor, and however
eredulously his disciples clung to this perverse interpretation of the Active Verbal
Noun (Nom. actionis) in Tagalog and in the dialects of several other tribes—in
the Bontoe Igorot Language the Verbal Noun is certainly not passive, but active
in its character.
*Here as in the paragraphs following I give only one of several examples.
For diacritical marks used with Bontok words, compare the original. (Rev,)
““Man” is but a lapsus for “our friend” ( Rev.)
° Agentis ? (Rev.)
REVIEWS. 279
If a passive is wanted, there is one on hand, in all times and moods of Igorot
(265-276): prefix ma--+ root + personal endings. Experiments with the Igorot
by means of their own vernacular (but not through interpreters) proved in-
disputably their correct consciousness of an active and a passive idea.
The fact that the Three Passives Fallacy has been propagated in good faith
for about two centuries and is still indefatigably copied and republished and
taught, shows (as also other factors do) how necessary it is to revise and to
compare the “Artes” of time-honored “authorities” and the entire material of
sacred books, catechisms, confessionals, prayerbooks, with the living dialects
spoken by the natives. The result of such future careful investigations into the
people’s vernacular, the collection of tales and songs in the unbiased dialects of
the different tribes ought to be most welcome to Comparative Philologists who
seem to rely only on the unreliable material at hand, fawte de mieux, material
collected by unphilological compilers, with a few admirable exceptions, such as
Totanes, Minguella.
The unfelicitous term of the Three Passives (which may have sprung from
its originator’s inability to distinguish between the Gerundium and the Gerun-
divum) was employed unscrupulously in many grammars and learned articles
and papers on various Philippine dialects, Bontoe Igorot excepted. The Three
Passives and their alleged application occur, for instance, in . . . [follows a list
of 25 authors, titles of books, and some comment].
THE VOCABULARY.
The vocabulary contains some 2,000 English catch-words, each of
which either is given one or more Igorot equivalents or is treated as a
theme developed into a summary of Igorot expressions for identical
and related ideas, always, however, with sharp discrimination between
words indigenous to the people and those borrowed from outside. “Verbs
are given first in the Present Active in their most common form (not
special form) ; the other “principal parts” follow: Preterite—Passive Par-
ticiple in Present—Nomen agentis. Personal Verbs are found in Present
and Preterite only.”° The basic form, the stem-word, of derivatives, for
which comparative philologists probably will look first, is not given.
The reason for this perhaps may be found in some remarks made by the
author in the preface to the vocabulary: “Is it necessary to warn against
using my Vocabulary any one who would, without having studied and
practiced the Grammar, attempt to derive any benefit from the Vocabu-
lary? ... The student of the Bontoc Grammar can easily construct and
supply the missing forms. The Author thinks he could do the same;
but he does not intend to depart from his principle: to write down only
what he has heard and as he has heard it.”
THE TEXTS.
A large amount of Bontok Igorot “Text” is found scattered throughout
the grammar in the shape of phrases taken down by the author from the
Igorots’ mutual conversation, and used by him as examples for illustrating
* Page 279 (Preface to the Vocabulary).
280 REVIEWS.
points of grammar and syntax. These phrases constitute very valuable
material for gaining an insight into that “language” which springs from
the mouth of the people as they work in their fields, attend to their
domestic affairs, go to war or chide, scorn, langh among themselves, ete.
It is precisely because, from the intelligent use made by the author of
such phrases, we can form a judgment as to the considerable insight
gained by him into the spirit of the language, that we wish he had
given them in the coherent form of some animated conversation among
individuals of the tribe. Could any other kind of “text” reflect more
truly the live speech of the people, or disclose more clearly the tem-
perament of the speakers? By this remark I certainly do not wish to
detract in the least from the great merit of the collection of folk-lore
that forms the third part of Doctor Seidenadel’s work and which also
contains examples of spirited conversation.
These texts, eleven in number, are:
1. LumMAwie, an extremely interesting and probably the most important story
of Bontok folk-lore, beginning with an account of how the (Bontok) world was
created and the Great Flood caused by two brothers, sons of Lumawig; how the
latter bade the sole survivors, a brother and sister, located on top of Pokis
Mountain, to marry, ordering his dog and the deer to furnish them the fire, ete.”
2. HEADHUNTERS’ RETURN AND CEREMONIES.
3. THE IGOROT IN THE BATTLE OF CALO/OCAN; a narration of the part taken
by a number of Bontok men in the action between the American and Filipino
forces at Caloocan, near Manila, on February 10, 1899.
4. THE RAT AND THE TWO BROTHERS; a graceful legend telling of the gratitude
of a rat, whose life had been spared by the younger of two brothers. The rat
makes presents to them both and the younger of the two, by a cunning exchange
gets possession of a magic spoon and pestle which when put into a pot will fill
it with meat and rice.
5. THE STARS; a spicy little tale, illustrating the quick-witted inventiveness
and satirical vein of the people who explain in it the origin of the [loko tax-
collectors of Spanish times.
6. Tiz1n; the metamorphosis of a girl into a rice-bird (tilin) as a warning to
parents who begrudge their children a liberal measure of food.
7. Korie, and
8. THE MONKEY, two more metamorphoses of children, as a warning to parents
who are too severe or neglectful.
9. PALPALAMA AND PALPALAKING; another story pointing a moral for greedy
people.
10. VARIA.
11. Songs; containing many words and phrases belonging to a “Song Dialect”,
words “of the old folks”, of forgotten or obscure meaning. which are of the greatest
interest to ethnologists and philologists.
Doctor Seidenadel has the merit of having overcome unusual difficul-
ties to enrich our knowledge of Philippine languages by a work containing
comprehensive and exhaustive information on the hitherto unexplored,
™Vaguely similar traditions exist in Ifugao folk-lore.
REVIEWS. 281
or at best very superficially known language of a people of northern
Luzon, who upon the downfall of Spanish sovereignty were taken charge
of by the American Government as crude head-hunters, and are now
‘being prepared for entrance into the comity of their civilized brother-
tribes. The compilation of an exhaustive grammar, ample vocabulary,
and representative collection of texts of their language is certainly a
means to bring them nearer our understanding, and to promote the task
just indicated. lo comparative Indonesian philology the complete re-
presentation of a member of the so-called Igorot dialects has always been
a desideratum ; thanks to Doctor Seidenadel this is now fulfilled and his
work is already being drawn upon in furtherance of such studies.
In the interest of the linguistic exploration of the Philippine Islands
it is to be hoped that Doctor Seidenadel will continue dedicating his
eminent talent to a task already so greatly furthered by him.
OTTO SCHEERER.
Allin’s Standard English-Visayan Dictionary. By Benjamin Casey Allin, gov-
ernment surveyor working in the Province of Cebu, Philippine Islands.
Cloth. Pp. 260. Falek’s Printing House, Cebu, Cebu, P. I.
This is a handy little volume designed for the use of Filipinos who
are learning English and of English speaking persons who are learning
Bisaya.
As there is no Bisaya-Hnglish section it could not be used by a person
who had no knowledge of English.
Tt contains over 5,000 English words listed alphabetically in the first
column. The second column contains the same words spelled phone-
tically, the third abbreviations indicating whether the word is a substan-
tive, verb, preposition, etc., and the fourth the definitions in Bisaya.
Tt is not quite clear why the compiler states that the letter “V” is
“used only in introduced Spanish words” and yet spells the name of the
language “Visayan” instead of Bisaya. ‘There is also a good deal of
difference of opinion as to the wisdom of representing by “aw” the final
sound ordinarily represented by “ao.” This sound in other countries
where the languages are being written phonetically is represented by “au.”
To many this seems more nearly to represent the sound and it certainly
would have the advantage, if adopted, of bringing Philippine philologists
into conformity with other students of the languages of the east.
There are many typographical errors in the book but probably none
of them so important as to interfere seriously with its usefulness.
One who has some knowledge of Bisaya or a considerable knowledge of
English ought to find the Dictionary useful.
M. L. M.
Ea ifs
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t ¢ t } ek ivf
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Lis a iy Gm iS ‘he Deh
Wee Re Ali wd
{ $ oe
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THE BONTOC IGOROT.
By A. E. JEnxs.
110 pages. 3 maps. 154 photographic plates. 9 figures.
Poe ede 1B P g
An interesting study; the result of almost a year’s residence among
the Bontoe Igorots.
Price $1 United States currency, postpaid.
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62 photographic illustrations. 91 pages.
An interesting ethnological study of the pygmy blacks of Zambales. ~
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THE PHILIPPINE
JOURNAL OF SCIENCE
D. GENERAL BIOLOGY, ETHNOLOGY
AND ANTHROPOLOGY
Vou. VI DECEMBER, 1911 No. 6
THE FISHERY RESOURCES OF THE PHILIPPINE ISLANDS.
PART IV, MISCELLANEOUS MARINE PRODUCTS. .
By ALVIN SEALE.
(From the Ichthyological Section, Biological Laboratory, Bureau of Science,
Manila, P. I.)
CONTENTS.
I. Trepang (Béche de Mer).
II. The Shark-fin Industry.
III. Philippine Sea Turtles and Tortoise-Shell.
TV. The Philippine Window Shell.
V. Philippine Shells Used in the Manufacturing of Buttons.
VI. Precious Corals.
VII. Edible Seaweeds of the Philippines.
VIII. The Preparation of Isinglass in the Philippines.
IX. Preparing Skins of Aquatic Animals for Leather.
X. A Check-list of Philippine Holothurians.
I. PHILIPPINE TREPANG (BECHE DE MER).
Trepang is a general name applied in the Philippines to all of the
many species of animals belonging to the group Holothurioidea and known
locally as béche de mer, balatan, bilate, munang, hisam, sea cucumber,
and cotton-spinner. Large quantities of these animals are gathered in
the Philippines for export to China and Japan. 'Trepang is a staple
food of all Oriental people and is an important item of export from the
Philippine Islands.
Trepang in general appearance resembles pickled cucumbers. The
106346 283
284 SEALE.
skin may be smooth, or covered with prickle-like teats arranged in rows
or scattered over the body. In color they range from pale flesh-color
to black. These animals, when dry, are hard, sausage-shaped, and appear
to be altogether unpalatable and it is not until they have been cleaned,
minced, and made into a most delicious soup by the skillful hand of
the Chinese cook that the real value of this product of the sea is
understood. Béche de mer live among the white sand and coral in the
sea-gardens and feed upon small sea-animals and sea-vegetation, so there
is no reason why they should not rank as a delicious food product and
come into general use among Huropeans and Americans. I can, from
experience, heartily recommend a trial of trepang soup* to those who
delight in a dish free from the contaminations of the land, with a delicate
aroma of the deep sea about it.
VARIETIES OF PHILIPPINE TREPANG.
In Manila all the large dealers in trepang are Chinese. They recognize
five different varieties, as follows:
No. 1.2—Oé (Plate I, fig. 1). A large, uniformly black, perfectly
smooth variety (H. atra Jeger). This species, when dry, is from 420 to
200 millimeters in length and 40 to 60 millimeters in diameter. This is
regarded as the most desirable species found in the Islands and sells for
the highest price, being valued at 65 to 98 centavos per kilogram whole-
sale, according to the size of the animal, and care in curing. I will
call it the great smooth black trepang.
No. 2.—Gan Sim (Plate I, fig. 2), is a large brownish trepang, with
two rows of teats on each side. The animal, when dry, is of a rather
flat, oval shape, about 120 millimeters in length and 60 millimeters in
width. Its back is but slightly roughened. ‘This species is regarded as
being next to the best variety, sells for 40 to 80 centavos per kilogram,
and is in fair demand. We will call it the great oval brown trepang.
No. 3—Bark Sim (Plate I, fig. 3) is the third grade of trepang and
to this belongs the great mass of trepang shipped from the Islands. It
includes a large variety of forms ranging in price from 35 to 70 centavos
*To make trepang soup.—Clean and wash out the trepang in cold water, slice
and put them in a chopping bowl and mince fine, soak in cold water five hours,
then boil for one hour, add salt and pepper and a quantity of beef or chicken
stock and bring to a boil. Serve hot. [Sing Fat.]
27 have been unable to find anyone in the Philippines who recognized or could
give me any information regarding the names given to the Philippine trepang by
Simmonds in his Commercial. Products of the Sea, although I have repeatedly
asked dealers and fishermen both in Jolo and Manila. It is possible that his
so-called “bankolungen” is the gan sim, his “munang” the oé, his “telepan” the
moi whar che, his “sapatos grande” the smooth white ringed bark sim, his
“sapatos china” is perhaps the great convoluted bark sim, and his “lowalowan”
is possibly the bark sim, called the small black wrinked trepang in the present
paper.
FISHERY RESOURCES OF THE PHILIPPINE ISLANDS. 285
per kilogram, the most abundant, perhaps, being small, black, slightly
roughened, cylindrical in shape, and when dry about 90 millimeters long
by 25 millimeters wide (Plate II, fig. 1). Another very common form
of this grade is the Philippine convoluted trepang, a large, light brown
species about 130 millimeters by 40 millimeters, cylindrical, with the
body, when dry, thrown into deep folds (See Plate II, fig. 5). Another
bark sim is a moderately roughened, cylindrical trepang of a dull yel-
lowish-brown color and 150 by 35 millimeters in size (Plate II, fig. 3).
Another is a dark brown, almost smooth form (when dry), with the back
covered with small orange spots with black centers. This is a large
species, 170 by 70 millimeters, and cylindrical in shape (Plate 4, fig. 4).
I will call this the smooth white-ringed trepang. Another form very
similar to the last I will term the rough white-ringed trepang. (Plate
II, fig. 2.) This trepang is 160 by 48 millimeters in size, cylindrical,
with the body decidedly tuberculate; it is rather dark brown in color
with numerous white circles around the large tubercules of the sides and
back. Another rather common trepang of the bark sim grade, is a small,
very black form, with deep wrinkles in the body (Plate II, fig. 6). This
variety when dry is cylindrical in shape and about 80 millimeters long
by 20 millimeters deep. I will call it the small black-wrinkled trepang.
No. 4.—Moi Whar Che (Plate I, fig. 4). This trepang is a large,
eylindrical black form, easily distinguished by the fact that the entire
back is covered with numerous, very long teats which are black or reddish
brown in color. ‘This variety is quite abundant, but is regarded as fourth
rate as a food product, the price being from 30 to 50 centavos per
kilogram. I will term it the great prickly trepang.
No. 5—Hong Che (Plate I, fig. 5) is the fifth grade of trepang, and
resembles the last except that it is smaller and more cylindrical; the
teats are more pointed and slightly longer. Its wholsale price is from
35 to 45 centavos per kilogram. Many of the young of the moi whar
che are to be seen in this class, but are distinguished easily by their
short teats. In size the hong che is from 50 to 90 millimeters in length
by 16 to 20 millimeters in width.
There are numerous other grades among the 63 species of these animals
found in the Philippines, but none are of sufficient importance or value
to be recognized in trade. However, one very common form, called “yel-
low belly,” is so abundant, especially about Mindoro, that is deserves at
least to be catalogued. This form when dry is yellow-white on the belly
and black on the back,.about 60 millimeters in length and 25 in depth;
its value is not above 12 pesos * per picul. It is only the great abundance
of this grade that makes it worth our consideration.
All of the above grades retail in Manila for fully 30 per cent advance
on the prices obtained by the fisherman.
* One peso is equal to 50 cents United States currency, and 1 picul is 139 pounds.
286 SEALE.
DISTRIBUTION, HABITS, GROWTH, AND PRODUCTION OF PHILIPPINE TREPANG.
The wide distribution of these apparently helpless, sedentary sea-
animals is a matter of interest and astonishment to all who give the
subject any thought. - Twenty of the species found in the Philippines are
also common to Polynesia, 16 to the Malay Archipelago, 30 to the Red
Sea and the coast of Africa, while 3 extend even to the west coast of
America. The majority of the recorded forms are believed to be well
distributed throughout the Philippines, but are most abundant in the
Sulu Archipelago. The supply for Manila comes chiefly from Tacloban,
Polillo, and Ambos Camarines. They are found in water of various
depths, even in very shallow water and also on reefs dry at high tide,
down to 137 fathoms and even to much greater depth. Sheltered places:
inside the coral reefs where the bottom is of coral sand seem to be favorite
haunts of the bark sim and hong che forms, while moi whar che, gan
sim, and o€ seem to prefer water of greater depth just at the edge of
the reef. The greater number of the trepang appear to pass large quan-
tities of sand and mud through their alimentary canals; from this sand
they extract the small animals and plants on which they feed. On
Arboles Reef, Gulf of Davao, Mindanao, I once noticed a large number
of Colochirus quadrangulus Less. feeding on sea-weed which at low tide
was about 75 millimeters (3 inches) under water. They were so abun-
dant that it was scarcely possible to step without treading them down,
and in one scoop of an ordinary dip net I secured 57 of them. It is
probable that during the season for depositing the eggs they all seek
the reefs or rocky crevices. Mitsukuri,t in his most interesting paper
on the common Japanese trepang, writes, referring to the Island of Oki,
The people there have for a hundred years or more been in the habit of putting
up loose stone-piles in the shallow sea in order to obtain a supply of this trepang.
Nowhere in the Philippines is this devise put into practice although it
doubtless would yield profitable results.
Practically nothing is known about the breeding time of the Philip-
pine trepang and it is a subject well worth investigating. In Japan (as
abstracted from the above paper), the trepang spawn in May and June,
and at the end of the first year have a maximum size of 5 by 25 centi-
meters. ‘They reach the adult condition at the end of the second year,
but do not spawn until the end of the third; some individuals probably
live two or three years after spawning. The young specimens are white
and transparent, and they attach themselves to the roots of alge, or seek
rocky crevices in sheltered localities. Hence a rock pile affords a
natural collecting ground for the very young as well as for the old.
Japan has put some measures in force setting aside certain localities as
4 Notes on the Habits and Life-History of Stichopus japonicus Selenka. Annot.
Zool. Jap. (1903-06), 5, 1-21.
FISHERY RESOURCES OF THE PHILIPPINE ISLANDS. 287
breeding reserves for trepang, upon which stone piles or dikes have
been constructed, and in these places fishing for trepang is strictly for-
bidden. In this way the Japanese hope to conserve this valuable food
supply.
There are so many natural breeding places in the Philippines along
the coast and among the rocks on the shore line of the many islands,
that our supply now is, and probably for years to come will be, much
greater than the demand, or rather more than the fishermen under present
conditions will take the trouble to dry and prepare for market.
METHODS OF FISHING FOR TREPANG.
In gathering trepang, the fisherman usually goes out at low tide wading
in the shallow water, dragging a small canoe or banca behind him, into
which he throws all the trepang he picks up;- sometimes he fishes
from a boat, with a long handled, one-pronged spear, with which he
gathers up the trepang in water of 3 to 4 meters. In water of greater
depth some fishermen dive and bring up the trepang in their hands.
There are localities where small dredges undoubtedly could be used with
good effect.
PREPARING TREPANG FOR MARKET. at
The Filipino method of preparing trepang for the market is to boil
them for a short time (from five to twenty minutes) in fresh water, after
which they are split up the belly, eviscerated, and then thoroughly dried
in the sun. Hach variety seems to require a slightly special treatment
particularly in regard to the length of time required for boiling, in
order to bring out the best flavor. However, they should all be heated
thoroughly throughout, and when taken out of the boiling water they
should be hard and elastic, and should dry quickly like a hard boiled egg.
The 0é frequently is boiled only five minutes; it should be well stirred.
Experience really is the only guide as to th; length of time required for
boiling. Sun-dried trepang are the best, and in the greatest demand,
but the method of sun-drying is too slow for preparing a whole ship-load.
The following method given by V. Simmonds ° is followed in preparing
large shipments of trepang.
The first thing to do on arriving at an island where trepang is plentiful is
to erect a curing house on shore. This house may be of any desired size but
one 30 meters long by 15 meters wide, with sides 4 meters high, will be found
convenient for preparing a ship’s cargo. This structure may be built of native
material such as mats, bamboo, etc., and roofed with a coconut thatch which
must be put on well to keep out the rain. A small door should be left in each
end of the house. Platforms for drying the trepang are then erected along
one side of the entire length of the house and these should be 2 meters wide, the
lower one about breast-high from the ground and the upper one | meter above that.
>The Commercial Products of the Sea. New York (1897), 111.
288 SEALE.
These are made of split pieces of bamboo or small slats. A trench 1 meter
in width and a half meter deep is then dug beneath the lower platform along its
entire length, for the fires. Tubs filled with salt water are placed at short
intervals along the trench, with buckets near at hand for use in preventing the
fire blazing up and burning the trepang or destroying the house.
The process of curing is as follows: The trepang is first caught and gutted
and washed in fresh water; it is then carried into the curing house and placed
on the lower platform where it is spread out about 14 centimeters (5 inches)
thick, to dry. When this platform is covered with the trepang, the fires are
lighted in the trench; they must constantly be kept going, day and night, and
be carefully guarded. Much skill is required in properly drying the trepang
as well as in boiling it, as too much heat will cause it to blister and get porous,
like a sponge, whereas too little will lead to its spoiling and turning putrid
within twenty-four hours after being boiled; care is requisite likewise in gutting,
for if this is not properly attended to the animals will turn into a blubbery
mass within a few hours after being caught. On the afternoon of the second
day after the fires are lighted, they are extinguished for a short time and the
trepang is shifted to the upper platform; splints of wood should be put in those
not properly drying. The lower platform is then filled again with a fresh
supply of trepang from the pots, and the fires are again lighted. The trepang
on the lower platform should be turned frequently during the first twelve hours.
After another two days the fires are again put out and the trepang on the upper
platform shoved over at one end to make room for those on the lower platform,
and the same proceeding repeated for the two following days, by which
time (six days in all) the first day’s product will be cured properly. The
trepang is then taken off the upper platform and carefully examined, those not
dry are put back again, and the quantity cured is stowed away in bags on
shipboard or in a dry storehouse. The product soon becomes damp, unless
packed in air-tight casks. If held in storage for three months, it requires to be
dried again for a short time in the sun.
Forty men are necessary to work a house of the above size to its greatest
capacity.
UTILIZING TREPANG AS FOOD.
The chief use of trepang as food is in the form of a savory soup,
as heretofore described. It is also eaten as a meat by certain natives
of the Philippines, after it has been roasted. In some islands of the
Busuanga group, the natives collect these animals and by irritation cause
them to eject a viscous white fluid which swells up greatly when it comes
in contact with sea-water and splits into numerous white threads,
not unlike cotton; these threads are cooked and eaten and are regarded
as a delicacy. However, as the animal frequently ejects almost all the
viscera as well as the mucus, the dish probably would not appeal to
Huropeans or Americans.
The Chinese believe that trepang is not only a most delicious food,
but that it also possesses excellent medicinal qualities.
QUANTITY AND VALUE OF EXPORTED PHILIPPINE TREPANG.
Sixty-six thousand eight hundred thirty-eight kilograms of trepang
were exported from the Philippines in 1909. The export in 1910 was
120,969 kilograms, which, at the low price for third grade quality, would
FISHERY RESOURCES OF THE PHILIPPINE ISLANDS. 289
be valued at 51,780 pesos. As a matter of fact much of it was first and
second grade trepang so that probably the true value would more nearly
approximate 75,000 pesos. According to British statistics, the Sulu Ar-
chipelago alone supplied Singapore in 1907 with trepang valued at 21,975
pesos. Singapore’s total trade in trepang for that period was valued at
442,102 pesos, two-thirds of which was shipped to Hongkong. It would
be much cheaper for Hongkong to buy directly from Manila; as a matter
of fact, our last year’s increase in export largely was due to the direct
buying of Hongkong dealers.
China imports each year about 3 million kilograms of trepang, chiefly
from the Malay Archipelago, Philippine Islands, and the South Pacific
Islands. The export from Manila might easily be doubled without damage
to the fisheries.
COMMERCIAL POSSIBILITIES IN PHILIPPINE TREPANG.
While it is true that trepang is one of the minor marine products of
the Philippines, nevertheless, we should not lose sight of the fact that it
is a staple and recognized article of diet with a country which has the
largest population on the face of the globe, and where it finds a ready
market; also, that it can be cheaply prepared, that the natural supply
in the Islands is large, and that with but little care the output probably
could be increased readily. Taking all these facts into consideration, it
is rather a matter of astonishment that large canning companies, espe-
cially in the United States, have not awakened to the possibility of this
product of the sea and added the delicious trepang soup to their list of
conserved products.
A check list of Philippine holothurians appears.at the end of this paper.
II, THE SHARK-FIN INDUSTRY IN THE PHILIPPINE ISLANDS.
The drying and curing of sharks’ fins (Plate III, fig. 1) in the Phil-
ippines, for export to China, is one of the minor industries, requiring
but little capital and yielding profitable returns. At present the business
is almost entirely in the hands of Chinese merchants.
The fins of all of the numerous species of sharks found in the Islands
are used, as well as some of the fins of the larger rays. The big, dorsal
fin of the shark is the most desirable; this is usually of a uniform pale
grayish or whitish color on both sides, and is supposed by the Chinese
to contain more gelatin than any of the others, therefore it commands the
highest price and is known in commerce as the “white fin.” All the
remaining fins, which include the ventrals, pectorals, anal, and caudal,
are classed together as “black fin.” The large caudal fin when uniform
in color is frequently put in as “white fin.” he fine white fins are
selected for the making of soup, while the black fins are largely used in
manufacturing a superior grade of fish glue.
290 SEALE.
METHOD OF CATCHING SHARKS.
Sharks are principally caught by the Moros, although they are captured
in considerable numbers in corrals and nets throughout the Islands. The
Moros usually spear them, or catch them with hook and line, using
stale fish for bait. The observer can not fail to be impressed by the
number and size of the sharks caught by the Samal Moros in the vicinity
of Sitanki Island.
A number of Philippine sharks will take the trolling spoon, especially
if it is painted red on one side; they afford very good sport. In India,
sharks are captured in large nets for the sake of the oil secured from
the liver; they are also used as food by the poorer classes. In the Phil-
ippines the Moros alone seem to relish shark-meat, and the manufacture
of fish oil is an entirely neglected industry. If we consider the great
number of sharks caught in these Islands, it is a matter of surprise to
find that the making of fish-oil is not carried on in connection with the
shark-fin industry, as this would very materially increase the revenue
_ derived from each shark.
THE PREPARATION OF SHARKS’ FINS.
The fins are cut from the shark as soon as possible after its capture, the
thick fleshy portions of the larger fins are slit open to facilitate their drying, and
they are then spread out in the sun. It requires from three to six days to
dry the product depending upon the amount of sunshine. After the fins are
thoroughly dry they are assorted into two grades: The white fins, or first class
variety, in which are placed all the large dorsal fins; and the black fins, or
second class, which includes all the small fins. They are then packed tightly
in bales of about 100 kilograms each and are ready for export.
These fins are further prepared by being soaked in boiling water for a short
time and the skin removed. They are then shredded into small cartilaginous
rods, somewhat resembling a very fine grade of sphagetti. These are waxy white
and attractive in appearance (Plate III, fig. 2).
At this stage they are either made into soup, or dried and reéxported to all
parts of the world at considerably more than double the original price. To make
this prepared fin into a savory and wholesome soup it is soaked in cold water one
day, then placed in hot water for one hour, this causes all the rods to separate.
Eggs and some chicken or beef stock, salt, pepper, and butter are added and the
mixture boiled for two hours. That the above receipt produces a most delicious
soup was the unanimous verdict of the staff of the Bureau of Science after testing
a sample prepared by Sing Fat, a well known Chinese cook of Manila.
No great Chinese feast is complete without a dish of this soup and I believe
it is worth while to call the attention of our large soup manufacturing estab-
lishments to the possibilities of this industry in the Philippines. I believe that
an almost unlimited market could be found in China.
THE AMOUNT AND VALUE OF SHARK-FIN EXPORTED FROM THE PHILIPPINE ISLANDS.
Sharks’ fins weighing 172,610 kilograms, valued at 85,000 pesos (42,500
dollars), were exported from Manila during the year 1910. The current
price of shark-fin at Zamboanga, which is one of the centers of the trade,
FISHERY RESOURCES OF THE PHILIPPINE ISLANDS. 291
is 84 centavos per kilogram for the white fin and 58 centavos for the
black, therefore, it is evident that the export valuation is very low and
that the real value probably would be somewhat over 100,000 pesos. The
price is subject to considerable variation. In 1909 the maximum price
paid for the entire yield was 2.19 pesos per kilogram including both white
and black fins. Chinese merchants in Zamboanga informed me that
the price for the first grade white fin sometimes reaches 6.58 pesos per
kilogram, but this is unusual. Almost the entire yield of Philippine
shark-fin is shipped to Singapore or Hongkong, and from these places
is distributed to various parts of China.
In Manila the retail price of prepared shark-fin, as shown in Plate III,
fig. 2, is from 8 to 10 pesos per kilogram.
In conclusion I wish again to call attention to the fact that the by-
products of the shark fishery are entirely wasted. If, in addition to
the fins, the liver was used to make fish oil, and the skin which is used
for scabbards for swords was also saved, the revenue derived from each
shark would be about doubled.
III. PHILIPPINE SEA TURTLES AND TORTOISE-SHELL.
VARIETIES OF PHILIPPINE MARINE TURTLES.
. Sea turtles of large size find a congenial home in the warm waters of
the Philippines. Abundant schools of fish supply them with plenty of
food, and the hot sandy beaches of numerous, small, uninhabited islands
furnish them ideal nesting places; hence, as a result of these conditions,
the three recognized species of sea turtles are found throughout the
Archipelago.
The marine turtles ° are easily distinguished from all other kinds by
the fact that their hmbs have become completely changed into paddles,
the fingers being entirely encased in a single skin, with one or two claws
only projecting. They swim swiftly in the sea, but are almost helpless
on the land, and if turned on their backs they can not regain their
normal position.
Our most important sea turtle, popularly known as the hawksbill
turtle, is Chelone wmbricata Linn. (Plate IV, figs. 3 and 4), which sup-
plies the tortoise-shell of commerce. It is easily recognized by the
fact that it has a hooked bill (Plate IV, fig. 4) and but 13 plates on the
back, which overlap like the shingles on a roof; in addition, there are
25 small plates which form the margin of the back. This turtle feeds
largely on fish, crabs, and mollusks, and when full-grown is about 1
meter in length.
* All members of the turtle family that live in the sea are called turtles;
those living on the land only are termed tortoises; and those living in fresh
water terrapins.
292 SEALE.
The green turtle (Chelone mydas Linn.) is next in importance. (Plate
IV, fig. 5.) This turtle has a straight bill (Plate IV, fig. 6), but the
shields on the back, while the same in number as in the hawksbill, are
perfectly smooth, evenly joined, and do not at any stage overlap. This
turtle is valued chiefly as food, the shell being of no value. However,
as an article of food it has from time immemorial been considered a great
delicacy. This species is herbivorous, and when adult it is about 1.25
meters in length. The flesh may be cooked in any desired way, either
roasted, used as soup, fricasseed, or made into stews or pies. The fol-
lowing method of cooking the plastron, or shell of the belly, is given by
Father Labat, a Dominican monk." Jt sounds so appetizing that I give
it in full.
The plastron or bluckler is the shell of the belly, on which is left three or
four inches of flesh, with all the fat, this being green, and of a very delicate
flavour. The plastron is placed in the oven. It is seasoned with lemon, capsicum
or cayenne, salt, pepper, cloves, and eggs beaten up. The oven ought not to be
too hot, as the flesh of the turtle being tender it should be cooked slowly. While
it is baking the flesh must be pierced from time to time with a wooden skewer,
so that the gravy may penetrate all parts. The shell is sent up to the table and
the meat carved out from it. I have never eaten anything more appetizing or
better flavoured.
There are large factories in various countries that can the soup made
of this turtle.
The third variety of marine turtle found in the Philippines is the
loggerhead (Thalassochelys caretta Linn.) (Plate IV, figs. 1 and 2).
This species is easily distinguished from either of the above from the fact
that it has 15 shields on the back and 27 around the margin of the
shell. The jaw is strongly hooked (Plate IV, fig. 2). It feeds on
crabs and other crustaceans. The shell is about 1.25 meters in length
when full-grown. The shell practically is of no value, being almost as
thin as paper (Plate V, fig. 4), and it is only used for veneering and
inlaying work. The price for which it sells is from 2 to 4 pesos per
kilogram. However, the animal supplies a large portion of the turtle oil
of commerce.
TORTOISE-SHELL,
During the fiscal year 1909 there were exported from the Philippines
2,040 kilograms of tortoise-shell valued at 34,942 pesos. During the
year 1910 the exportation fell to 1,191 kilograms, probably owing to
home buying and domestic use.
The hard, bony plates which cover the back (carapace) of the hawks-
bill turtle are the tortoise-shell of commerce (Plate V, fig. 1). There
are 13 of these plates on the back of each turtle, 5 in the center and
7 Simmonds, Commercial Products of the Sea. New York (1895), 367.
FISHERY RESOURCES OF THE PHILIPPINE ISLANDS. 293
4 on each side. In commercial terms these are known as 8 “sides,” 2
“hoofs,” 1 “skull,” and 2 “main” plates. The two middle side-plates are
of the greatest value, being the largest and thickest. Plates 17 by 30
centimeters in diameter with a thickness of 5 to 6 millimeters are not
unusual in the Philippines. In addition to these large plates, there are
25 small ones around the margin of the shell; these are known as “hoofs”
and are of much less value. All of the plates together are known as a
“head” of shell, and tortoise-shell nearly always is sold by the “head.”
Practically all the Philippine tortoise-shell is brought into the market
by native fishermen. Now, while a small number of these turtles is
captured by fair means, with hook, net, spear, or trap, by far the greater
number is taken when they come ashore to deposit their eggs. The
fishermen are so eager to secure their prizes that as a rule they do not
give the poor turtle a chance to deposit her eggs before they kill her.
This short-sighted policy eventually will result in the destruction of the
fisheries unless the turtles are protected during the breeding season, which
is from May to August. The turtle fishermen go to small, uninhabited
islands, frequently many miles from the large islands surrounding the
Sulu Sea, and wait perhaps days for the turtles to come ashore to deposit
their eggs. If the men are in no especial hurry they may wait until the
turtle has deposited her eggs, which sometimes are 150 to 200 in number,
and about the size of hens’ eggs, with. tough leathery shells. The fisher-
men then kill her before she can reach the water, and dig up the eggs
which they use as food. The islands of Bancoran, Lumbucan, Arena,
Cavilli, and others in the Sulu Sea, are well-known nesting places of the
turtle, and it is only necessary to visit these islands to see the destruction
wrought during the nesting period.
The best method of removing the tortoise-shell from the back of the
turtle is to immerse the back in boiling water until the shell loosens;
another method is to bury the body in the sand for eight days, when the
shell becomes loosened; still another is to hold the shell over a slow fire
until loosened. This latter process usually is employed. In some coun-
tries the live animal is held over the fire until the shell is loosened ; it is
then turned loose “to grow another shell.” This method is barbarous,
not only for its cruelty but also for its lack of utility, for the animal
promptly dies.
WORKING AND WELDING TORTOISE-SHELL.
The methods employed in the working of tortoise-shell are quite similar
to those used in working horn. As a matter of fact, horn frequently
is used as an imitation of tortoise-shell. Slow heat or steam is em-
ployed, the shell becoming plastic by immersion in water of 90°C. for
two minutes. When cool, it retains any shape given it while hot.
i
294 SEALE.
The exact technique * of welding tortoise-shell is as follows:
When two pieces of shell are to be joined, the two edges are beveled so that
one inclined edge may lie upon the other. The edges are scraped perfectly clean,
contact with the fingers or any greasy substance being carefully guarded against.
A piece of paper is then bound around the overlapping edges and fastened
with a string. A pair of flat tongs or pincers, something like hair-dresser’s tongs,
are then heated and applied to the shell, one jaw of the pincers above and the
other beneath, by means of which the shell is grasped throughout the length of
the seam or overlap. By holding it a short time in this position, the heat of
the iron penetrates through the paper, softens the shell, and causes the two
pieces to unite firmly. Sometimes two pieces of shell are united by means of
boiling water as follows: The two edges are overlapped, two pieces of metal are
placed along the joining, the shell is placed in a press, and the whole is immersed
in boiling water. As the shell softens, the press is screwed more tightly, by
which the two pieces of shell become firmly united. Owing to the fact that the
shell becomes mobile with heat, it is easily molded into almost any desired shape
by means of boiling water and the screw press, and even small bits of shell
are utilized by being thus welded together. If too much heat is used the shell
becomes blackened, consequently in many places, especially in Japan, most of the
work is accomplished by hand graving, following a pattern as in scroll work.
The same method is followed in Manila, where the outfit of the workman
consists simply of scraper, saws, files, and a bench. Manila has two small
factories employing about six men (all Chinese), where crude combs (Plate VI, —
figs. 1 to 6) of tortoise-shell are made. There is also a small factory in Iloilo.
All the work in this place is done by hand and is of the crudest sort.
The method used to weld tortoise-shell in Japan differs in slight detail.
Dr. Shigeho Tawaka of the Zoological Institute, College of Science, [m-
perial University of Tokyo, kindly supplies the following information.
First of all, shells which are to be welded are just dipped in water and thus
moistened, the shells are then put in between two thin pieces of magnolia
wood (Magnolia hypoleuca) and then the whole thing is moderately pressed with
a pair of heated pincers which have been dipped in water an instant before
operating (a hissing sound is the usual sign of these being sufficiently heated).
The welding of the shell is thus completed. The reason why they use the magnolia
pieces is to avoid the direct contact between the heated pincers and the shell.
The temperature of the pincers is not scientifically made known, being said to
be the trade secret kept among the preparators.
The appearance of tortoise-shell frequently is given to horn by brushing
it over with a paste made of two parts lime to one part litharge, and a
little soda lye, which is allowed to dry on. Artificial tortoise-shell is
manufactured by melting gelatine and various metallic salts.
VALUES AND GRADES OF PHILIPPINE TORTOISE-SHELL.
It is very difficult to arrive at a true valuation of tortoise-shell, owing to its
variations and the reluctance of the Chinese merchants, who now control the
trade, to give out any facts regarding the matter, but 4 different grades are
5 Simmonds, Commercial Products of the Sea. New York (1895), 355.
FISHERY RESOURCES OF THE PHILIPPINE ISLANDS. 295
recognized. Two of the principal merchants of Zamboanga give the value of
the first grade (which is not often found), as 50 pesos per kilogram while 2
principal dealers in Balabac quote the value of the first grade at 167 pesos per
kilogram. These prices were quoted to customs officials. The value of the
second grade is from 16 to 20 pesos per kilogram. A considerable portion of the
Philippine shell falls in this grade (Plate V, figs. 1 and 2). The third grade
is thinner and is valued at from 11 to 13 pesos per kilogram, while the fourth,
consisting of small shell is valued at 4.16 to 8 pesos per kilogram. It usually is
sold by the catty, which is equal to 1.39 pounds.
The value of tortoise-shell depends not only on the size and thickness
of the plates, but also largely upon the coloring and marking, there being
a great variation in the beautiful clouded and mottled patterns in the
shell. The color most in demand at present seems to be the rather dark
shell with but few light spots. Golden-colored combs, at one time greatly
prized and to-day much used by ladies with blond hair, are made from
the plates of the plastron or belly. The price of the shell also depends
largely upon the prevailing style in ladies’ hair dressing as well as upon
the fashion in toilet articles. However, the demand for good tortoise-
shell seems steadily. to be increasing. Japan is the center of the work for
oriental countries.
POSSIBILITIES OF TORTOISE-SHELL WORK IN THE PHILIPPINES.
* Personally I have seen nothing in the Philippines which seems to offer
so sure a return to a man with a small amount of capital, say 6,000 to
10,000 pesos, as the buying and working of tortoise-shell. The machinery
required is but little. The manufactured articles would enter the United
States duty free, thereby finding a ready market. The supply of shell
is, on the average, about 2,000 kilograms per year, which would be suffi-
cient to keep a small factory in operation and I have no doubt that the
returns would be remunerative. The main difficulty would be to induce
the Chinese middlemen to deal directly with the factory rather than with
Shanghai or Singapore (the two places that take practically our total
yield). A man who could buy directly from the fishermen would have
a still larger profit.
CULTIVATION OF THE TORTOISE.
The cultivation of the hawksbill turtle has never been undertaken in
the Philippines, but it is not improbable that it could be cultivated to
advantage in much the same way as is the edible turtle (Tryonyx japonicus
Schlegel) in Japan. It is a subject worthy of consideration not only by
private individuals but by the Government. A careful study of the habits,
nesting places, rate of growth, and food of the hawksbill and green turtles
should be undertaken with artificial cultivation in view, and if thought
practical, steps should be taken to establish turtle farming, for practical
and experimental purposes.
296 SEALE.
IV. THE PHILIPPINE WINDOW-SHELL.
DESCRIPTION.
In the majority of windows in the city of Manila, the pane is of shell
instead of glass. ‘The shell used for this purpose is called kapas or
window-shell (Placuma placenta Linn.).
This shell (Plate VII, fig. 2) is thin and flat with a rounded outline,
and somewhat resembles a very large wafer. The entire shell including
the animal is about 1 centimeter in thickness (Plate VII, fig. 1) by 14
centimeters in diameter. ‘The left side (valve) of the shell is slightly
convex, the right side is flat. The right side is easily transformed into
a windowpane simply by squaring off the edges with a big pair of scissors
or a crude machine such as is used for cutting plug tobacco. The shells
are then framed and are ready for use. ‘The size of shell most in demand
will square 7.5 centimeters, although those that square 6.5 centimeters
are also much used. ‘The opinion prevailing among the general public
regarding window-shell is that it is a slab of shell split off from some
larger shell. This, needless to say, is entirely erroneous, as the window-
shell is used in its natural condition, the two halves being torn apart
and the edges merely trimmed. ‘The left side of the shell is convex and
hence is in but small demand. Windows made of these shells are trans-
lucent, admitting a soft light, very grateful to the eyes in a tropical
country.
The windows present a most attractive appearance (see Plate IX,
fig. 1) and consequently are used in some of the handsomest structures
in Manila, such as the American Cathedral, the new General Hospital,
and the new Young Men’s Christian Association building; and while
they increase considerably the beauty of this type of architecture, they
are also peculiarly adapted to, and make a most attractive appearance in,
buildings of the bungalow style. -
DURABILITY AND STRENGTH OF THE WINDOW-SHELL.
These windows of-shell last for generations. Some of the old churches
of Manila have shell windows which have been exposed to the weather for
over a hundred years and which are still serviceable. Shell windows are
easily repaired, as a new shell is readily sprung into place when one
becomes broken or worn.
The strength of these thin, wafer-like shells is something astonishing.
Below is given a table showing the relative strength of window-shell as
compared with plate glass 2 to 3 millimeters in thickness by actual test
in the Bureau of Science.® It is shown by this table that window-shell
is much stronger than plate glass 3 millimeters in thickness. The
°The tests were made by W. C. Reibling of the laboratory of inorganic and
physical chemistry, Bureau of Science.
FISHERY RESOURCES OF THE PHILIPPINE ISLANDS. 297
relatively poor showing of the Capiz shells probably is due to the fact
that they were old and very dry; they also were somewhat smaller than
those from Cavite.
Table showing the strength of window-shell compared with plate glass.
Number of falls of a steel ball weighing | Number of
3.55 grams, necessary to produce failure on | blows neces-
samples 2.54 cm. wide and supported at |sary to produce
both ends 5 cm. apart. failure with 1
Aver- ae eine te | kg. ecient a
Material tested. | ,28¢ | Weight Height of fall. Pe eaaaerenal
Hale Per falling tem,
: ae 7 high on speci-
| men 7 by 7 cm.
and supported
50 em. 100 em. 150 cm. at both ends 6
em. apart.
Capiz shells __-_- 6 to 73.
Cavite shells ____ 390 to 1,500.
1,
2.
GENERAL ANATOMY OF THE WINDOW-SHELL.” See Plate VIII (a-l).
These shells when alive are more or less transparent and in younger
specimens the functions of the animal may readily be observed through
them. Old specimens are thickened and opaque.
The,largest and most striking object that attracts attention upon opening a
window-shell is the mantle, or pallial lobe (Plate VIII, fig. a), which lines the
interior of the shell, the margin of which has numerous, fine, finger-like projections
forming the pallial fringe (fig. b) ; the mantle usually is much pigmented. When
the left valve is removed and the left pallial lobe cut away, the 4 scimitar-
shaped gills or branchiew are exposed (fig. c). Near the center of the shell is
the round, hard adductor muscle (fig. d) which has been cut in order to open
the shell. Directly above the muscle, surrounding the stomach, is the large,
yellowish-green liver (fig. e) ; directly to the right of this is the large, yellow,
genital lobe (fig. f).; originating just above the highest point of the gills is the
foot (fig. g), a long tube-like organ extending to or beyond the edge of the mouth
and ending in a disk which is usually full of mud. On the opposite side of the
shell is seen a structure slightly similar but much smaller and ending in a disk;
this is the anal funnel (fig. h). The intestine extends up to the stomach. Near
the base of the foot, between two, thin, flap-like membranes, the labial palps
(fig. i), is found the small, slit-like mouth. Between the lower genital lobe and
the muscle will be seen a delicate, thin-walled organ, the heart (figs. j and k),
consisting of 2 auricles and 1 ventricle. The aorta, with some of its large
branches, is on the top of the liver. To the left and near the muscle are the
kidneys, or nephridia (fig. 1); dark colored, elongate organs. By dissecting
between these and the muscle, a long, curved, cartilage-like rod is exposed. This
is the crystalline style; it is inclosed in a sac, the pyloric cecum.
* For a detailed and accurate account of the anatomy and histology of Placuma
placenta L. we refer the reader to the excellent work of James Hornell, F. L. S.,
of the Madras Fishery Bureau, in a Report to the Government of Baroda on
the Marine Zoélogy of Okhamandale in Kittrawar, Part I (1909), 43-99, 5 pl.
298 SEALE.
The nervous system is similar to that of other members of this order, being
composed of the following three ganglia: (1) The cerebral ganglion may be seen
by folding back the labial palps; it is a large, pale, orange-colored mass halfway
between the base of the palps and base of the foot. (2) The pedal ganglion is on
the base of the foot in the middle on the dorsal side. (3) The parieto-splanchnic
ganglion will be found on the lower front curvature of the muscle close to the
extremity of the kidneys. The byssus and byssus gland are absent.
DISTRIBUTION OF THE PHILIPPINE WINDOW-SHELL.
The window-shell is widely distributed throughout the Islands in
certain definite areas. A large bed exists in Manila Bay, especially in
the shallow arm of the bay east of Cavite known as Bacoor Bay. It is
also found at Paranaque; in fact, the entire east end of the bay from
Paranaque to Cavite is a potential bed for the window-shell. Kawit is
the center of activity for window-shell fishing for the Manila Bay beds.
Important beds also oceur at Pangolao and Talibon in Bohol, at Valla-
dolid in Oriental Negros; in Capiz, Masbate, and Lloilo; in the Province
of Pangasinan, Luzon, and in numerous localities in Mindanao. Doubt-
less, there are a number of other places in the Islands where this shell is
found which have not been reported. Iloilo supplies large quantities of
shell for the Manila market. Shells from the Province of Pangasinan
seem to be uniformly thicker and more opaque than Iloilo shells, but
average slightly less in size, being 112 and 107 millimeters in diameter.
In no place in the Philippines are these shells fished for the pearls
which they sometimes contain, but always for the shell alone.
HABITS, CULTIVATION, AND FOOD OF THE WINDOW-SHELL MOLLUSE.
The window-shell mollusk is usually found in shallow water, but has
been known to exist in a depth up to 20 fathoms. It requires a bottom
of grayish or bluish mud where more or less fresh water is carried in by
streams.
There is a large variety of marie life found in the Manila beds,
such as large quantities of clams and edible oysters; in fact, the cul-
tivation of the oyster and the window-shell is carried on simultaneously
by a number of fishermen. The oyster beds are staked off by their re-
spective owners, and when fishing for window-shell or oysters outside of
their claims, all the small and half-grown window-shell oysters are col-
lected and planted on their oyster farms and kept there until they are
mature. The young shells can not be sold as they are not large enough
for windows. The adults keep the claim well supplied with spat.
The owners of these claims club together and hire a watchman, who
is stationed in a house built over the water near the claims.
The yield of the Cavite beds is estimated at 14,000 adult shells for a good
week’s fishing. However, the fishing is intermittent, depending pon the demand
and also upon the owner’s need of ready cash. The shells are fished entirely
at low tide in water of 1 meter or less in depth; the fishermen feel for them
FISHERY RESOURCES OF THE PHILIPPINE ISLANDS. 299
either with their toes or their hands, just as the fancy strikes them. Adult
shells are rather scarce on the public fishing grounds of these beds. I secured but
35 in one hour of fishing, but in ten minutes an owner of one of the planted
beds secured 100 adult shells for me. These measured 118 to 135 miilimeters
in their greatest diameter.
The shell matures in three years. At the end of the first year it is 62
to 83 centimeters in its largest. diameter. ‘The sexes are separate, the
egos being fertilized in the water. The mature ova have a decided resem-
blance to the form (in outline) of the mature shell, while the spermatozoa
have globular-shaped heads and extremely long tails, fully 10 to 15
times the length of the head. It is a comparatively easy matter to
fertilize the ripe ova under artificial conditions by taking the ripe
spermatozoa of the male in sea-water or normal salt solution.
The artificial fertilization and cultivation of this important com-
mercial mollusk is well worth our careful consideration, and it is to be
hoped that with the opening of the salt-water aquarium and _ fish
hatcheries having running salt water, that the study of the life and
cultivation of this shell will be made with great care and detail.
The food of the window-shell mollusk consists of small marine or-
ganisms, chiefly diatoms, which it collects from the water. The window-
shell mollusk apparently does not moye about, but lies flat on the mud
on its convex, left side. The foot, instead of being a means of locomotion,
is used to keep the mud from the gills and other organs.
QUANTITY OF SHELL AVAILABLE AND PRICES DEMANDED.
The supply of this shell in the Philippines is so large that at no
place has it been found necessary to resort to diving for it, as is done
in India, as plenty of shell is secured by wading in water less than 1
meter in depth and feeling about with the toes.
There are no laws regulating the gathering of window-shells, and so
far as we have been able to ascertain there are no municipal ordinances
relating to them.
It is estimated that there are 5,000,000 of these window-shells used
each year in the City of Manila alone. A single lumber company of this
city in 1910 used 1,500,000. The demand is increasing.
The price depends upon the size. Shells that will square 63 milli-
meters (2.5 inches) sell for 3 to 7 pesos (1.50 to 3.50 dollars) per
thousand ; while the large ones which square 7.5 centimeters (3 inches)
sell for 8 to 10 pesos (4 to 5 dollars) per thousand. One window-shell
fisherman explained to me that he had three prices for the first-grade
shells. These were valued at 8 pesos per thousand to the Filipino, 10
pesos per thousand to the Spaniard, and 12 pesos per thousand to the
American.
The Chinese traders do not hesitate to.ask the amateur buyer 15 pesos
per thousand. he shells usually are sold in large baskets, each holding
10,000 pieces.
106346——2
300. SEALE.
The window-shell is not exported to any extent, the only shipment
for last year being 1,458 kilograms sent from Iloilo to New York. How-
ever, it is expected that when the builders of bungalows in the United
States, especially in California, recognize how much stronger, cheaper, and
more attractive these shell windows are than the same thickness of glass,
there will be a brisk demand for them in that country.
"HOW WINDOW-SHELL IS USED.
Shell windows are made of narrow strips of wood usually 13 to 18
millimeters wide and 13 millimeters thick, or they may be any size
desired. These strips are grooved on two sides and notched every 6.0
or 7.5 centimeters as the case may be, to receive the cross stick which
also is notched; thus a solid square frame is formed for each shell.
After these are put together the entire square is set in a solid frame to
fit the window or door. (Plate IX.)
The following uses are also suggested for the shell:
Screens.— (Plate IX, fig. 2.) These shells make a most attractive and useful
screen, made up either in three divisions in the usual form of the Japanese
sereen, or else in a single division like the Spanish screen.
Lights for verandas.—(Plate I, figs. 1, 2, and 3.) These shells make a most
durable and desirable light for open yerandas, as they lend themselves to a
great diversity of forms, the shell being easily trimmed to fit into any form of
opening. The old-fashioned lantern shape is a popular form for these lights.
Old mission shade lights (Plate X, fig. 3) are most attractive and serviceable;
they are usually made up with hard-wood frames and large window-shells.
Conservatory windows.—These shells would be found most desirable by the
owners of hot-houses or conservatories in countries where hail is prevalent or
where the direct rays of the sun are too strong; they admit a soft light with
a fair amount of heat, and the expense as compared to that resulting from
breakage and painting or frosting of glass would be almost nothing.
Fronts to kitchen cabinets—These window-shells would make up into most
attractive fronts for kitchen cabinets, being easily kept clean and not liable
to breakage. 5
A dozen other uses might be suggested for window-shells. We can
most highly recommend them for almost any purpose to which opaque
glass would ordinarily be applied, and I feel confident that, when their
cheapness and utility are recognized in the United States, they will be
exported in larger quantities.
VY. PHILIPPINE SHELLS USED IN THE MANUFACTURE OF PEARL BUTTONS.
In addition to the pearl-oyster shells, which are exported from the
Philippines in large quantities,” there are three varieties of shells found
in these Islands and used in the manufacture of pearl buttons. These
™ Names of Philippine dealers from whom window-shells may be obtained in
quantity, can be obtained by applying to the Bureau of Science.
“See This Journal, Sec. D (1910), 5, 87 to 101 (with 6 plates).
FISHERY RESOURCES OF THE PHILIPPINE ISLANDS. 301.
are the great top shell (Trochus niloticus Linn.), the green snail (T'urbo
marmoratus Iinn.), and the chambered nautilus (Nautilus pompilius
Linn.).
THE GREAT TOP SHELL.
The great top shell (Trochus miloticus Linn.) (Plate XI, figs. 1 to
4) known locally as the lock, conic shell, trochus, susong-dalaga, or
samong, is a large, conical, top-shaped shell, found in abundance in many
islands of the Philippine Archipelago. Aside from the true pearl oyster,
this shell is the one in greatest demand for manufacturing buttons. As
a matter of fact, owing to its cheapness, it is frequently made into
buttons in preference to employing the pearl oyster. The great top shell
when mature is from 10 to 15 centimeters in diameter and a trifle less
in height; it has many close whorls, the largest of which flares decidedly.
The shell is marked with radiating or zigzag bands of red, violet, or
brown; the aperture is oblique and has a spiral operculum. An adult
shell 10 centimeters in diameter weights 330 grams.
The great top shell is usually found at low tide near the outer edge
of coral reefs or under large rocks, and while small quantities may be
encountered on almost any coral teef in the Archipelago, they are espe-
cially abundant in the vicinity of Sitanki, along the coast of Pangasinan,
and Ambos Camarines, Luzon, and on the northern coast of Palawan,
the eastern coast of Samar, and in the vicinity of Masbate. ‘There are
also numerous places on-the coasts of Mindoro where they are abundant.
I noticed a number of these shells washed up on the beach on the
eastern side of the Gulf of Davao.
The soft portion of the great top shell is regarded by the Filipinos
as a very fine article of food and, as a matter of fact, this species of
mollusk is more sought after for its meat than for its shell. One proof
_ of this is in the numerous piles of empty shells to be found on the
beach im localities near the ocean. It is usually noticed that they have
been placed on the fire, in order to cook the animal, after which it is
easily removed from the shell. Of course, shells treated in this man-
ner are spoiled so far as their commercial value is concerned. The proper
way to remove the animal is to place the shell in hot water, as the shell
is in no wise injured by this treatment.
So far as my experience shows, the great top shell is always more
or less solitary and while five or six are frequently found under one large
stone they never occur in beds or in great numbers over a given limited
area.
The average annual export of this shell from the Philippines during the
past four years has been about 350,000 kilograms valued at about 60,000
pesos. ‘The price fluctuates greatly. For a considerable period the stand-
ard price was 7.50 pesos per picul for middle grade shells. The Manila
302 SEALE.
button factory, in 1910, was paying from 10 to 22 centavos per kilogram,
depending on the grade. A small quantity of shell sent to the United
States was sold for about 22 centavos per kilogram (5 cents gold per
pound). Japanese button factories offered to buy, in large quantities,
half-grown shells for 28 pesos per picul of 137.5 pounds. During May
the price for great top shell in Zamboanga was 18 pesos per picul.
During the past few weeks the price has fallen to 12 pesos.
The establishment of a second button factory in Manila, together
with the evident desire on the part of American button factories to secure
Manila shell, no doubt, are responsible for the increase in the price. The
result will certainly be greatly beneficial to the trade as it will stimulate
the gathering of these shells and the native fishermen will soon learn
that it is more profitable to bring them to market than to destroy them
by fire in order to extract the animal for food.
The one objectionable feature which must soon be taken into consideration is
the desire of the Japanese buyers to secure the young, half-grown shells. It is
very evident that if the young shells are taken it will not be long before there are
none left to propagate. However, this is a condition that may easily be remedied
by legislation. An adequate export duty on great top shells of less than 9
centimeters (3.5 inches) should be imposed at the earliest possible date.
No careful study has been made in the Philippines of the reproduc-
tion, habits, rate of growth, food, or the possibilities of artificial cultiva-
tion of this commercially important shell.
THE GREEN SNAIL SHELL.
The green snail shell (Turbo marmoratus Linn.) (Plate XII, figs.
1 to 4) known locally as turbo, sea snail, /along, or bulolo, is a large.
heavy, turban-shaped shell, found throughout the Philippine Archipel-
ago, and largely used in the manufacture of buttons. It is not in as
great demand as the great top shell, as it is considerably harder to work,
and of less desirable color, having an opalescent instead of a pure white
luster.
The green snail is the largest of the turbo family, sometimes reaching ©
a diameter of 20 centimeters. ‘The usual size is about 16 centimeters;
the whorls are few, more or less knobbed; the body whorl is the largest ;
the aperture is nearly round.
The color of the shell is a rich green, mottled or spotted with brown
and white. The very old shells lose much of the brown color, and show
continuous bands of white following the whorls. When the rough outer
layer is removed they are of a beautiful, opaline mother-of-pearl color
inside and out.
In addition to being made into buttons they are also a favorite shell for
cabinets, spoons, and drinking horns. The royal family of Scandinavia from
time immemorial have had these shells studded with gems, mounted with silver,
and formed into royal drinking cups.
FISHERY RESOURCES OF THE PHILIPPINE ISLANDS. 303
The animal is highly esteemed as food by the Filipinos and is eaten
in Japan also, where it is made into chop suey.
The green snail is found in the greatest abundance at the edges of
coral reefs and in water several fathoms deep. It is also to be encoun-
tered along rocky shores under large boulders. The small islands in the
vicinity of Cebu yield a considerable quantity. It is also fairly abundant
along the coast of Negros and Masbate. The northern coast of Palawan
also yields a large supply.
About 100,000 kilograms of the green snail shell are exported from
the Philippines annually. The price paid to the fishermen ranges from
7.50 to 11 pesos per picul of 63.25 kilos.
As in the case of the great top shell, very little is known of the life
history, habits, reproduction, or the possibilities of artificial cultivation
of this shell in the Philippines.
THE CHAMBERED NAUTILUS.
The chambered nautilus (Nautilus pompilius Linn.) (Plate X, fig. 4)
is so well known that a description is unnecessary. It is world-wide
in distribution and is an inhabitant of water of from 300 to 350 fathoms
in depth. China seems to be the only country that manufactures this
shell into buttons, consequently its export from the Philippines is prac-
tically limited to that country.
The chambered nautilus is obtained in large numbers along the southern coast
of the Island of Negros, sometimes as many as 3,000 nautilus shells being gathered
in this region during one season. They are frequently caught in fish traps and
are sold as a sort of “by-product”. at 10 centavos each, although when brought
into market the very fine, large specimens sell for much more. In many
countries these shells are fashioned into spoons, vases, and pearl ornaments.
A practical as well as an ornamental use has been made of these shells by the
author, who has them mounted on red coralline, set in a solid base of red
cement and with an electric globe fitted to the inside of the shell. This makes
a most satisfactory reading lamp. (Plate X, fig. 4.) In Paris these shells are
used for making the finest grades of cameos, and ornamental objects of pearl.
They are among the most striking common shells in all museum cabinets. In
New York City dealers charge from 2.50 to 5 dollars each for nes large shells.
Unfortunately the New York market is limited.
However, there is an increasing demand for these shells for the pur-
pose of export, and some fishermen are found who give their entire time
to catching nautilus. Ordinary bamboo fish-traps with funnel-shaped
entrances are used. ‘These are baited with crab and lowered into deep
water, mm a day or two they are drawn up and the nautilus removed.
The Filipinos eat the flesh to a limited extent.
SUGGESTIONS FOR ESTABLISHING BUTTON FACTORIES IN THE PHILIPPINES.
_ Judging from the numerous letters of inquiry received by the ichthy-
ological section of the Bureau of Science from various parts of the world
regarding the establishment of button factories in the Philippines, this
304 | SEALE.
is a subject of sufficient interest to warrant giving the following sug-
gestions:
Location of factory—Manila, Cebu, Iloilo, or Zamboanga would be a good place
for the establishment of a button factory. The cost of renting a suitable
building for a factory in either of these places would not exceed 50 dollars per
month. A building would cost somewhat more than a similar structure in the
country or coastwise districts in the eastern United States.
Labor.—The laborers would be Filipinos. They are found quite satisfactory
by the Manila button factory, the pay in this factory being from 5 to 10 pesos
per month, ten-hour days. :
Power.—Steam or gasoline power would probably be found most satisfactory,
although in all the places mentioned, except Zamboanga, electric power could
be obtained. Wood as fuel is quite out of the question; coal costs from 10 to
14 pesos per ton in Manila. At Zamboanga water-power might be secured.
Gasoline in Manila sells at from 4.50 to 5.00 pesos per 10 gallons; petrolewm
costs 1.40 pesos per tin of 5 gallons.
Taxation—A manufacturer’s license, costing 2.40 pesos, is required, and. the
internal revenue tax is one-third of 1 per cent of the gross receipts, payable
quarterly.
Amount of shell available—The amount of shell ayailable for button making is
about 450,000 kilograms of great top and green snail shell and 300,000 kilograms
of pearl shell, making a total of about 750,000 kilograms (1,675,000 pounds)
of shell per year.
Bleaching shell for button making.—A large portion of the button trade is
‘with the Chinese and they require a very white button, consequently a bleach
of some sort is necessary. The following method, given by Robert R. Williams of
the laboratory of organic chemistry, Bureau of Science, is effective and cheap.
“Many processes are in existence for the bleaching of ivory, horn, and shell for
ornamental or other purposes. When chemicals are used those having a solvent
or oxidizing action on the organic matters-in the horn or shell are chosen.
Nowadays the most commonly used agent is hydrogen peroxide which may be
had very reasonably in Europe and America. It is not feasible to use it at a
distance from the factories making this chemical because of the deterioration in
transit. Therefore it is more practicable to use a metallic peroxide and generate
the hydrogen peroxide when needed. Barium or sodium peroxide may best be
used, preferably the latter. The follewing process has been tested on shell
buttons and found satisfactory. The buttons are first immersed in fuming
sulphurie acid for ten to fifteen minutes. The acid is then drained off and may
be used repeatedly if kept in well stoppered bottles. The buttons are then
rinsed three times with water and covered with a 5 per cent solution of oxalic
acid. Ordinarily 1 liter of buttons will require 1 liter of solution, though
more is necessary for large or dark-colored buttons than for small or light ones.
The oxalic acid solution should be kept ice cold if possible or at least below 20°
C. Commercial sodium peroxide is now added in small quantities with constant
stirring till the solution is alkaline to litmus paper. About 40 to 45 grams will
be required per liter according to the purity of the chemicals. A very little of
the 5 per cent oxalic acid solution is now added till, after stirring, the solution
reacts acid to litmus. It is important that the solution be acid, but a large
excess of acid is to be avoided.
“The buttons are allowed to lie in this solution for 24 to 72 Agmns according to
their size and color. Bleaching proceeds better and more rapidly if the buttons
are exposed to direct sunlight while lying in the liquor. This can be done in
colorless glass jars which, if possible, should be tightly stoppered.
FISHERY RESOURCES OF THE PHILIPPINE ISLANDS. 305
“The buttons after removal from the bleach liquor may be washed with water
containing a little hydrochloric acid. This removes the encrustation from the
outside and brings out the luster. After washing again with water they are
ready for the further processes of manufacture.
“Tt will be found that buttons can be bleached effectively by this means
and that the strength of the shell is increased by the deposition of caleium
oxalate in the interior.”
VI. PRECIOUS CORAL.
A small spray of true precious coral (Corallium sp.) was found on the
beach of the Gulf of Davao, Mindanao, directly in front of the small
station called Vigas. This specimen resembled very closely a species of
Japanese precious coral (C. japonicum Kishinouye).
As it is not improbable that considerable quantities of precious coral
eventually may be discovered in the Islands, it seems worth while to
give a short description of this article of commerce, and to describe the
methods employed in coral fisheries.
DESCRIPTION OF PRECIOUS CORAL.
The precious coral of commerce in its natural state closely resembles a
small shrub, or the branch of a tree from which the leaves have been removed.
Each stem and twig of this coral shrub has a hard central axis, or skeleton.
Outside of this and similar to the bark on a plant is the thin soft covering or
skin, which is easily rubbed off when fresh and is friable when dry. There are
numerous small holes in the “skin” through which minute, flower-like animals
project when the coral is alive; these are the coral animals (zoids) ; each of them
has 8 small arms or tentacles around its mouth, with which it gathers food.
All of these zodids are connected by a vascular system inside of the skin.
The hard part or skeleton is the valuable portion of the coral. It is made up
of fused spicules consisting of carbonate of calcium with a small amount of silica
and magnesia. The structure is concentric with radiating lines. The entire
skeleton is very. hard and so compact that no pores can be seen in a cross-section
without the aid of a lens. This furnishes an easy test for distinguishing the
precious coral from the numerous varieties of no value.
In color these corals range from white or delicate pink to dark red. Precious
corals reproduce sexually, and by budding. The reproductive organs are internal
and attached to the faces of the mesenteries; they shed their contents within the
body where fertilization takes place. The precious corals are believed to be
viviparous. Colonies are sometimes composed entirely of males, sometimes entirely
of females, frequently all on one branch are males, while all on another branch
of the same colony are females. Occasionally both sexes are combined in one
animal, forming a hermaphrodite. The eggs contain a considerable amount of
yolk and when hatched the larval forms are free swimming and may move a
fair distance before they settle and become fixed.
The food of the precious corals consists of living organisms; they have been
known to eat the powdered flesh of fishes.
VARIETIES AND DISTRIBUTION OF PRECIOUS CORALS.
The best known species of precious coral is Corallium nobilis Pallas, more
generally known under its synonym of O. rubrum Linn. This species is found in
the Mediterranean Sea off the northern coast of Africa, also off the coast of
306 SEALE.
Tunis, Sardinia, Italy, Corsica, and at the Cape Verde Islands. Hight species of
precious coral have been described from Japan. These are Corallium japonicum
Kishinouye, C. elatiws Ridley, C. boshuensis Kishinouye, C. suleatwm Kishinouye,
C. pusillum Wishinouye, C. imutile Kishinouye, 0. confusum Moroft, and C. konojoi
Kishinouye. Two species, C. johnsoni (Gray) and OC. maderense (Johnson), are
found in Madeira. C. stylasteroides (Ridley) occurs in Mauritius, C. regine
(Hickson) is found in Timor, and C. secundum (Dana) has been found at Banda,
Iti Islands and in the Hawaiian Islands. This constitutes the entire list of
established species of precious corals known to the present time.
The vertical distribution of these corals in the sea varies from 5 to 500 or
more fathoms. They are found attached to rocks, dead shells, or dead coral;
some species seem to prefer overhanging, submarine cliffs.
In general the vertical distribution of the Japanese species ranges from 50
to 180 meters, while in the Mediterranean fisheries the work of obtaining the
coral is usually carried on in waters of much greater depth.
FISHING FOR PRECIOUS CORAL.
Fishing for precious coral is almost always carried on by means of various sorts
of dredges. In Japan the dredge consists of a rectangular bag net about 1.5
meters wide and 1 meter high, with a 13 centimeters mesh, this is fastened to
a frame of bamboo, tufts of old netting are fastened to the lower edge of the
net and at the sides. These collect many broken coral branches. The coral
fishing boats are allowed to drift over the banks with the sails at half mast. The
net is allowed to touch the bottom and proceeds with a jerking motion. When
the fishermen think they have secured or fastened to coral they pull up the net.
The dredge used in the Mediterranean coral fisheries is of wood in the shape
of a large cross with a heavy stone attached to the extremity of the lower
arm and with coarse, twine bags of large mesh and with numerous tangles of
frayed ropes attached to the anterior arms. Numerous variations of this, as well
as ordinary tangles, are also used. ;
USES AND VALUE OF PRECIOUS CORAL.
The chief use of precious coral is in the manufacture of coral beads and
ornaments. It is first sorted into different grades, of which there are several
recognized in commerce; it is then cut into suitable pieces and all necessary holes
are drilled in it. It is then filed into any shape desired, and engraved. Next
it is polished with pumice stone and water, followed by a polish of very fine
chalk and water. Oil is never used on coral.
The value of precious coral depends upon its color, form, and quantity. A
string of large uniform beads may be bought in Italy for 20 pesos, while a string
of beads of similar size but of the best quality will cost 400 pesos. Japanese
precious coral in its native state sells for from 100 to 500 pesos per kilogram, and
the best Mediterranean sells for twice these amounts.
The export value of coral from Japan is about 500,000 pesos per year.
THE CULTURE OF CORAL.
The culture of precious corals has not received the careful scientific attention
that it should.
C. noblis has been kept alive for some time in aquaria, and if it were planted
under natural conditions possibly it could be grown with profit. Careful ex-
perimenting along this line might lead ‘to useful and valuable information.
FISHERY RESOURCES OF THE PHILIPPINE ISLANDS. 307
LITERATURE ON PRECIOUS CORAL.
KisHiInouyE, K. Notes on the Natural History of Corals. Journ. Imp. Fisheries
Bur. (1904), 14, 1-32, (13 plates).
KiraHara, T. On the Coral Fisheries of Japan. Journ. Imp. Pisheries Bur.
(1904), 13, 1-14 (5 plates).
THOMPSON and HENDERSON. Report on the Aleynarian Corals Collected by the
Investigator. Pub. Indian Mus. (906), pt. I, 120.%
WricHt and STUDER. Challenger Report (1889), 31, 185.
Jounson, J. Y. Notes on the Corallidae of Madeira with Descriptions of two
New Species. Proc. Zool. Soc. (1899), 57.
Riptey, 8. O. On the Arrangement of the Corallide, with Descriptions of new or
rare Species. Proc. Zool. Soc. (1882), 221.
Dana, J. D. United States Exploring Expedition. Zoéphytes. Phil., (1846),
8, 641.
LACAZE-DUTHIERS. Histoire Naturelle du corail. Paris (1864).
Mororr. On a New Species of coral from Sagami Bay, Japan. Zool. Jahrb.
Syst., (1902), 17, 404.
BLUE CORAL.
In numerous localities throughout the Philippine Archipelago a fine quantity
of blue coral, Heliopora cwrulea Linn., is found in considerable quantities, usually
in water of from 2 to 10 fathoms depth.
This coral is a beautiful, permanent, cerulean blue in color. It takes a fine
polish and is found in large heavy masses. No doubt it could be used in jewelry
and ornamental work. No amount of polishing, however, will entirely obliterate
the pores. I have collected this coral at Jolo, and at Butuan, Mindanao, on the
eastern coast of Samar, and on the northern coast of Palawan. No use is made
of it at the present time, but as a body for broaches, bracelets, etc., it would
be very beautiful or as a background for pearls it would, in my judgment, be
unsurpassed.
RED ORGAN-PIPE CORAL.
The red organ-pipe coral (Tubipora spp.) is very common throughout the
Philippines. It has no especial value, its only use apparently being for cabinet
specimens. It is a shallow-water form. I have seen large blocks of it used with
other corals in the construction of a wharf.
REEF CORALS.
The common reef corals comprising a great variety of genera and species,
which have as yet never been identified, are used largely in the building of roads
throughout the Islands. They are employed to a limited extent in the manufacture
of lime.
BLACK CORAL.
The so-called black coral (Antipatharia sp.) is very common in the Philippines.
Fine specimens several meters in length and from 5 to 15 millimeters in diameter
are common throughout the Jolo Archipelago. It is also found in larger quantities
in the Gulf of Davao, Mindanao and near Cebu. It is usually secured in water
of from 10 to 20 fathoms.
The U. S. 8. Albatross dredged large quantities of this “insulated cable wire”
as it was called by the sailors and this term, indeed, is fairly descriptive of the
body of this coral; however, the branches are very numerous and give the small
corals a decidedly shrub-like appearance.
“This report includes a complete bibliography relating to corals.
308 SEALE.
This coral is used chiefly for making canes, as it is easily straightened or
bent. into any desired shape by immersion in hot water for a short time. It takes
a most beautiful jet-black polish and could doubtless be used in the manu-
facture of coral beads and rosaries. A cane of this coral nicely prepared and
polished can be bought for from 5 to 10 pesos. The raw material has very little
value at present.
VII. EDIBLE SEAWEEDS OF THE PHILIPPINES.**
Im connection with the series of articles on minor marine products,
it has been thought advisable to include what is known regarding the
edible seaweeds, with the hope that the publication of the meager data
available may stimulate interest in the subject. Below is given a list of
the species known to be used for food, and it is confidently expected that
eventually it will be greatly extended as data on the subject become
available. Very little seems to have been published on the subject.
The determinations have kindly been made by Dr. M. A. Howe, of the
New York Botanical Garden. The list is for the most part based on a
collection made by Eugenio Fénix of the Bureau of Science, in Union
Province, Luzon, supplemented by some local observations in and about
Manila. ;
In most parts of the Philippines, along the seashore, various species
of marine alg or seaweeds are found, although in this Archipelago as
in most tropical countries, these are not found in masses, or in such
great quantities as is the case with many forms in temperate regions, at
least in shallow waters.
The first impression on studying Philippine alge is that the number of species
is very limited, but intensive collecting has brought to light a considerable
number and, doubtless, as botanical exploration progresses, the list of Philippine
alge will be greatly increased. In some regions the marine alge play no small
part in the economy of the natives, a considerable number being used for food,
thus entering into the local commerce.
At the present time a large percentage of our material is unclassified. Doubt-
less very many of our species are used for food, but collectors have given this
phase of the subject comparatively little attention, so that the data on the
utilization of local marine alge are very fragmentary.
Seaweeds are used for food both raw, in the form of salads, and
cooked sometimes with vegetables, such as tomatoes, and sometimes
with the addition of sugar, forming the dish, popular among the natives,
known to the Tagalogs as gulaman. It is probable that in Manila, at
least, a large part of the gulaman is made from prepared seaweeds im-
ported by the Chinese, although the local product is almost always to be
found in the markets. In Manila various species of alge are known
as gulaman, but the most important appear to be Aghardiella sp. (Fucus
gulaman Blanco), and Gracillaria confervoides (L.) Grev.
“Data supplied by H. D. Merrill, botanist, Bureau of Science.
FISHERY RESOURCES OF THE PHILIPPINE ISLANDS. 309
Aghardhiella sp. (Huews gulaman Blanco). This species is common in
Manila Bay and is universally known to the Tagalogs as gulaman. It is probably
the most generally used species in Manila, and during certain seasons is almost
always to be found in the native markets.
Chaetomorpha crassa (Ag.) Kiitz. Known in Union Province as cauat-cauat,
and locally used for food.
Codium tenue Kiitz. Known in Union Province as pupu-lo; edible.
Enteromorpha intestinalis L. This green alga is abundant in brackish
water about the mouths of streams, and is eaten by the natives to some extent.
Eucheuma spinosum (L.) J. Ag. Known in Union Province as rupruppuue ;
edible. ;
Gracillaria confervoides (L.) Grey. Abundant in Manila Bay at certain
seasons, locally known as gulaman, and sold in the native markets of Manila.
Gracillaria crassa Harv. Used for food in Union Province; known to the
Tlocanos as susueldot-baybay. sie
Gracillaria eucheumoides Harv. Known in Union Province as canot-canot ;
edible. i
Gracillaria lichenoides (L.) Grey. Known in Union Province as guraman;
edible. The above four species are allied to a Japanese species largely used in
the manufacture of agar-agar.*
Halymenia formosa Hary. Known in Union Province as gamet; there used
for food. An allied spécies found in Manila Bay, native name unknown, is
doubtless also edible. ;
Liagora cheyneana Harv. Known in Union Province as baris-baris; edible.
Sargassum siliquosum J. Ag. Known in Union Province as aragan, there
used for food. Widely distributed in the Philippines, as are several other
species of the genus, all of which are doubtless utilized to a greater or less
extent as food. :
VIII. THE PREPARATION OF ISINGLASS IN THE PHILIPPINES.
The preparation of isinglass is an industry that could be carried on
easily in the Philippines, but so far as I have been able to ascertain, it
has never been inaugurated.
Isinglass is the purest form of commercial gelatin known; it is pre-
pared from the “sounds” or air-bladders of certain fishes.
The preparation is very simple and requires no outlay of capital. The
exact method of procedure is as follows:
Remove the air bladders (also called “maw”, “swim bladder”) from the
fishes soon after they are caught, slit them open and wash thoroughly, take
off any thin membranes which envelop them. Then expose to the air to stiffen.
If oily, wash in lime water, then in fresh water and dry. They should be put
to dry on “flakes” or nets so the air will have free access to all parts. It is
sometimes desirable to give slight pressure in which case they may be dried
between sheets of paper, or flat driers, like botanical specimens. When thoroughly
dry they are put up in convenient packages and are ready for market,
The well known seaweed-isinglass, or agar-agar of Japan, is made from
an alga of the genus Gelidiwm. This genus has not yet been reported from the
Philippines.
310 SEALE.
USES OF ISINGLASS.
Probably the chief use of isinglass is in fining liquors of various sorts,
especially the best grades of wine. It is also used in the preparation of creams
and jellies, in stiffening fabrics, and in lustering ribbons. Isinglass is also used
in the manufacture of court plaster, artificial pearls, diamond cement, and
imitation glass.
It is true that owing to the expense of securing pure fish isinglass, agar-agar
prepared from seaweed, is used largely as a substitute. However, there is no
question that pure, fish isinglass is more desirable and gives better results in
almost all cases than the vegetable product.
FISHES FROM WHICH ISINGLASS IS SECURED.
The best grade of isinglass is secured from the sturgeon and is put up
in Russia. In the Malay Archipelago a very fair grade of isinglass is
secured from the fishes called thread-fin and from certain species of cat-
fish and croakers. In the Philippines, a profitable source of isinglass
could be found in the thread-fin, Polydactylus plebeius (Brouss.), called
mamali in Tagalog, and tatik in Moro. It is a very common fish in
the Manila markets, and ranges in length from 35 to 50 centimeters.
The common catfish (Netuma nasuta Bl.), called kanduli in Tagalog,
which is very abundant, especially in Laguna de Bay, also supplies a good
grade of isinglass. In addition, there are several species of croakers,
(Otolithes argenteus Kuh] & Van Hasselt), (Otolithes leuciscus Guuth.),
and Johnius belengeri C. & V.), and at least two species of Umbrina, from
all of which isinglass can be secured. The above are all common market-
fish and it has been estimated that the isinglass thrown away from them
is greater in value than the price secured by the fisherman for the entire
fish. ;
VALUE OF ISINGLASS.
The current value of isinglass quoted from a late trade journal is as
follows:
Russian isinglass, 2.75 to 3 dollars per pound; American isinglass, 0.73 to
0.75 dollar per pound; 14,000 pounds were imported into New York during the
month of April, 1911.
There seems to be no local demand for this product, but, owing to
the recent tariff regulation, it would enter the United States duty free:
consequently, it could be exported from the Philippines with profit.
IX. PREPARING SKINS OF AQUATIC ANIMALS FOR LEATHER.
CAYMAN OR CROCODILE SKIN.
(Crocodilus porosus Schneider and C. palustris Lesson.)
For commercial purposes, skins of the medium-sized cayman, of about
3 meters.(9 feet) length, are the most desirable as they are easier to tan,
and make the best leather. The skin should be cut along the middle line
of the belly from the chin to the tip of the tail and carefully removed
FISHERY RESOURCES OF THE PHILIPPINE ISLANDS. 311
from the animal soon after its death. Fine salt in sufficient quantity
should then be rubbed thoroughly into the raw side of the skin. It is
then rolled compactly and placed in a dry place to cure; occasional
examination should be made to see if it is curing properly. When
thoroughly cured the skin is ready for tanning.
To tan, it is first soaked in a tub of clear fresh water from two to six days—
depending on the size of the skin,—a 3-meter skin requires about five days.
It is then placed in a rather weak solution of lime and water which should be
increaséd in strength daily for about ten days. The wet skin is now placed on a
. smooth beam, raw side out, and all the fat or flesh rubbed or shaved off. It
is then placed in a thick mixture of bran and water and allowed to soak for one
day—this is to neutralize the alkali of the lime. During all of the above processes
through the solutions it is better if the skin be agitated occasionally so that
all parts receive sufficient treatment. The hide is then washed and immersed
in a tank of tanning extract. Any of the native tans may be used, or oak bark,
gambia, or sumac liquid of 4 per cent strength, and stronger liquid is added
each day until the strength has reached 20 per cent at the end of eighteen days.
The length of time will vary according to the size of the skin, strength of the
solution, or the color desired. The hide is then hung up to dry and harden.
It is then shaved and cleaned again so as to leave it of the desired thickness.
Tf black, red, brown, or green shades of color are desired the skin is put into
a bath of wood and aniline dyes, for about three-quarters of an hour. It is
then stretched out and nailed to a board or wide frame for drying. When dry
it is rubbed briskly over an iron or wooden beam to make it flexible.* The
skin is then ready for use. The price paid for prepared skins is from 2 to 4
pesos per 20 lineal centimeters.
So far as I have been able to learn no serious attempt has been made
to prepare the Philippine crocodile skin for leather. It is an experiment
well worth trying, as the cayman is notoriously abundant in many streams
of the Philippines.
WATER-SNAKE SKINS.
(Lapemis hardwickii Gray, Chersydrus granulatus Schneider, and other species.)
There are great numbers of water snakes in the Philippines. I have
seen more than one hundred brought in with one haul of an ordinary
fish sein on the Malate beach. It is quite probable that a good industry
could be built up in tanning the skins of these snakes for leather. Many
of them are finely marked and would make attractive belts, card cases,
and ornamental objects. Considerable quantities of snake-skin leather
are used in France. The following is the method of preparation:
The skins are removed from the animals and soaked for ten days in a strong
solution of sulphate of zinc. They are then fleshed, scraped, washed by hand, and
placed in a bath containing 100 parts water, 10 parts borax, 100 parts boracic
acid, 25 parts tartaric acid, and 25 parts saturated solution of precipitated
alumina. They remain in this bath one day and are then transferred to bath
No. 2 containing 1000 parts water, 25 parts phosphate of zine, 25 parts
benzoate of aluminium, 50 parts glycerine, 20 parts alcohol. The skins are
© Report U. S. Fish Comm. (1902), 350. —
ele SEALE.
left one day in this solution, then they are placed in the first bath again for
one day, then. back into the second for another day, this alternating of baths
being continued for five or six days, by which time the tanning is complete.
The skins are then dried, lightly staked, and finished off.
PREPARING SHARK SKIN.
Shark skin is used for a great many purposes, especially for sword
grips, knife and sword sheaths, for polishing wood and ivory, and for
covering small ornamental objects, such as jewel boxes or card cases.
A manufacturer in Paris has made a big reputation by tanning the skin
of the Malabar shark into morocco leather.
Some yery beautifully marked sharks are found in the Philippines
such as Chiloscyllium indicum (Gm.), Stegostoma tigrinum Linn., Sey-
Ilium capense Mull. & Hen., and S. marmoratum Gray & Hard. Their
skins could be made into excellent leather.
To tan shark skins, the skins are (if hard) first soaked in water for four
or five days; they then are placed in a solution of lime and water, as in the case
of the crocodile skins; they remain in this solution from two to six days, and are
then washed free of lime, and soaked in bran water for a day or so; they
are then fleshed, or shaved, and immersed in an alum solution composed of 0.5
kilogram of alum and 0.1 kilogram of salt to 4 liters of water; they remain in
this solution two or three days, with occasional stirrings. On removal they are
dried and are ready for manufacturing.
To prepare shark’s skin for the use of cabinet-makers it is merely cleaned and
not tanned, the hard dry skin is soaked in lukewarm water for three or four
days, shaved on the flesh side, and then dried. This skin will outwear many sheets
of sand-paper of equal size.
We are indebted to Chas. H. Stevenson’s valuable paper regarding
methods of tanning, for much of the above information.**
X. A CHECK LIST OF PHILIPPINE HOLOTHURIANS.
1. Cucumaria conjungens Semper.
General color brownish, MHabitat: Mariveles, Luzon. In shallow water.
Length 20-25 millimeters.
2. Cucumaria longipeda Semper.
Color dull gray. Habitat: Bohol, Pandanon. In water of 30 fathoms. Length
20 millimeters.
3. Cucumaria citrea Semper.
Color orange-yellow. Habitat: Bohol. In 8 fathoms. Length 15-20 milli-
meters.
4. Cucumaria versicolor Semper.
General color olive-green. Habitat: Bohol. In water of 6 to 10 fathoms.
Length 6-7 centimeters.
5. Cucumaria maculata Semper.
Habitat: Bohol. In water of 10 fathoms. Length 4.5 centimeters.
™ Report U. S. Fish Comm. (1902), 283.
FISHERY RESOURCES OF THE PHILIPPINE ISLANDS. 313
6. Cucumaria mirabilis Théel.
Habitat: Cebu, at the depth of 100 fathoms.
7. Cucumaria canescens Semper.
Habitat: Bohol. In water from 6 to 30 fathoms. Length 1.5—-3 centimeters.
8. Miulleria nobilis Sel.
General color dusky. Habitat: Bohol. In shallow water.
9. Milleria mauritiana Quoy & Gaim.
Habitat: Philippines. In shallow water.
10. Milleria lecanora Jeger. ‘
General color dirty yellowish. Habitat: Philippines. In shallow water up to
6 fathoms.
11. Psolus complanatus Semper.
- General color grayish. Habitat: Zamboanga. In shallow water. Length 22
millimeters.
12. Psolus boholensis Semper.
Upper portion gray, lighter below. Habitat: Bohol. In water from 6 to 17
fathoms. Length 15 millimeters.
13. Psolus boholensis pandanensis Semper.
Habitat: Bohol at Pandanon. In water of 30 fathoms.
14. Thyone villosa Semper. 3
General color yellowish-brown. Habitat: Philippines. In water of 10 fathoms.
Length 20-30 millimeters ‘4
15. Thyone rigida Semper.
General color grayish brown. Habitat: Bohol. In 10 fathoms.
16. Thyonidium cebuense. Semper.
General color brownish gray. Habitat: Cebt. In 10 fathoms. Length 30-35
millimeters. :
17. Echinocucumis adversaria Semper.
General color grayish. Habitat: Bohol. In 30 fathoms. Length 8-10 milli-
meters.
18. Haplodactyla molpadioides Semper.
General color pale-violet or lavender. Five branching papille around the anal
pore. Habitat: Bohol, CebG. In 13 to 20 fathoms.
19. Haplodactyla molpadioides pellucida Selenka.
Habitat: CebGi. Shallow water.
20. Chirodota rigida Semper.
Color light brown with whitish dots. Habitat: Bohol.
21. Chirodota incongrua Semper.
Sixteen tentacles, each with 18 to 20 digits. Habitat: Camiguin Island.
Shallow water.
22. Chirodota dubia Semper.
Tentacles 18, each with 18 to 20 digits. Habitat: Camiguin Island. Shallow
water.
23. Chirodota variabilis Semper.
Tentacles 17 or 18, each with 20 to 24 digits. Habitat: Mariveles, Luzon.
314 SEALE.
24. Chirodota panaensis Semper,
Habitat: Panay. Shallow water.
25. Synapta dubia Semper.
Habitat: Bohol. In water from 6 to 10 fathoms.
26. Synapta pseudo-digitata Semper.
Habitat: Bohol. In water of 15 fathoms.
27. Synapta molesta Semper.
Habitat: Philippines. In shallow water.
28. Synapta reticulata Semper.
Habitat: Philippines. In water of 8 fathoms.
29. Synapta indivisa Semper.
Tentacles 13, each with about 20 very long slender digits. Habitat: Zamboanga.
30. Synapta nigra Semper.
Digits of tentacles united by web at base. Habitat: Bohol. In shallow water.
31. Synapta grisea Semper.
Color in life greenish-gray, arranged in spots and bands, the ground color being
a dirty light-green. Habitat: Bohol. In water from 4 to 6 fathoms.
32. Synapta glabra Semper.
Color dark yellowish-brown above, yellowish below. Habitat: Ceba, Bohol.
Length 500 millimeters. Found in water from 4 to 6 fathoms.
33. Synapta innominata Ludwig.
Habitat: Manila Bay.
34. Synapta recta Semper.
Thirteen tentacles, with very short digits. Habitat: Bohol. In water of 6 to 8
fathoms.
35. Synapta gracilis Semper.
General color whitish with slight wash of yellowish-brown. Habitat: Manila
Bay.
36. Synapta beselii Jeger.
Color in life greenish. Habitat: Cebti reefs.
37. Synapta similis Semper.
Pinkish-white, with some brown anteriorly. Habitat: Bohol. In shallow
water.
38. Ocnus pygmzeus Semper.
Upper color greenish, the underparts yellowish-brown. Habitat: Bohol. In
water of 9 fathoms. Length 10 millimeters.
39. Ocnus imbricatus Semper.
General color yellowish-brown, lighter below. Habitat: Bohol. In water of -
8 to 15 fathoms. Length 35-40 millimeters.
40. Colochirus coeruleus Semper.
General color pinkish and green with markings of yellowish. Habitat: Bohol.
In water of 10 fathoms. Length 18-20 centimeters.
41. Colochirus viridis Semper.
General color sea-green. Habitat: Zamboanga, Mindanao. In shallow water.
42. Colochirus cucumis Semper.
Habitat: Bohol. In 6 fathoms. Length 3 centimeters.
FISHERY RESOURCES OF THE PHILIPPINE ISLANDS. 315
43. Colochirus anceps Selenka.
General color orange, the feet red. Habitat: Bohol. Shallow water up to
10 fathoms. Length 8-10 centimeters.
44, Colochirus cylindricus Semper.
Habitat: Bohol. In water of 10 fathoms. Length 5 centimeters.
45. Colochirus tuberculosus Quoy & Gaim.
Habitat: Bohol. In shallow water and up to 10 fathoms.
46. Colochirus quadrangularis Less.
Habitat: Bohol. In shallow water and up to 10 fathoms.
47. Stichopus variegatus Semper.
Yellowish-gray with markings of gray and brown. Habitat: Philippines.
In shallow water up to 10 fathoms.
48. Stichopus naso Semper.
General color yellowish-gray. Habitat: Bohol. In 10 to 15 fathoms.
49. Holothuria marmorata Jeger.
Auburn above, with some large spots or bands of yellowish-white; yellowish
below. Scattered over the sides of the body are violet spots on a yellowish-white
area. The deposits in the body wall are X-shaped, or oval with central incisions
on each side. Habitat: Bohol. In shallow water.
50. Holothuria tenuissima Semper.
Pedicels all over the body. The deposits consist of incomplete rosettes, or
slightly branched rods. Habitat: Bohol, in 15 fathoms of water.
51. Holothuria similis Semper.
Fine papillx all over the body. Habitat: Bohol, in 10 to 15 fathoms of water.
52. Holothuria erinzeus Semper.
Color dark-brown or blackish, lighter below; pedicels a light yellowish-brown.
The rods bear a few spines on their sides, their ends are slightly branched or
perforated. Habitat: Bohol and Luzon, in shallow water.
53. Holothuria graffei Semper.
Ventral pedicels in three distinct longitudinal series. The dorsal , papille
large. The deposits consist of tables, rosettes, and irregular branched plates.
Habitat: Luzon.
54. Holothuria pulchella Selenka.
The ventral pedicels are more crowded than the dorsal papille. The spire of the
table consisting of a reduced almost annular disk, with 12 teeth on the top.
Habitat: Philippine Islands, in shallow water.
55. Holothuria pervicax Selenka.
Color in alcohol grayish-brown, with some darker cross bands on the back.
The pedicels and papilla are about the same size. The ventral surface is more
crowded. The tables are not well developed, the spire being short and terminating
in but 4 teeth; disks small, rounded, smooth or slightly uneven on the margins.
Rods small, elongate, and uneven on the margins, or with holes on the sides.
Habitat; Philippine Islands.
56. Holothuria atra Jeger.”
Dorsal papille and ventral pedicels of nearly equal size. Disks forming simple
rings; often with small hole at the base of each vertical rod. The spire ter-
minating in 8 horizontal and 4 vertical teeth. The plates are evenly rounded, or
106346——3
316 SEALE.
undulated on margins, often with X-shaped branches. Habitat: Philippine
Islands, in shallow water.
57. Holothuria edulis Lesson.
Color a dark reddish-brown, light gray on sides and belly, a minute, dark ring
around the base of the pedicels. The dorsal papille are very minute and more
scattered than the ventral pedicels. Disk of the tables reduced to a small ring
more narrow than the top of the spire, which, when seen from above, presents
a small circular hole surrounded by 4 prominences, each with 4 or 5 teeth.
Habitat: Bohol, in 10 to 20 fathoms of water.
58. Holothuria monacaria Lesson. :
Color yellowish white, speckled with brown or greenish-brown on the back.
The young specimens are auburn, with the ventral surface white. The papille
paler. The dorsal papille are arranged in 4 indistinct longitudinal rows. The
rounded disks of the tables have a central hole surrounded by 4 to 12 holes. The
spire terminates in 12 teeth. Habitat: Zamboanga, in shallow water. Length
110 millimeters.
59. Holothuria vagabunda Selenka. :
The color varies from a dark brown to a reddish-brown. The table >ave small
disks; the spires terminate in 8 to 10 teeth placed around a 1 ireular
aperture at their top; buttons with 6 holes; the dorsal ped’ Save
supporting rods, these are spinous and taper towards the ends
pines, in shallow water.
60. Holothuria fusco-cinerea Jeger.
Color dusky-red, with some darker transverse bands on the 5 E able
never seem to attain the usual length of the spire, nor to have the umber
of transyerse beams. Habitat: Bohol, in 6 to 10 fathoms of water. neth 222
millimeters.
61. Holothuria immobilis Semper.
Color on dorsal surface brown, with some darker spots or bands, belly dirty
yellowish-white inclined to brown anteriorly. Tentacles 26; ventral surface with
pedicels, the dorsal surface with papille. The disks of the tables spinous; the
buttons irregularly formed, with about six holes. Habitat: Bohol, in from 6
to 8 fathoms of water.
62. Holothuria coluber Semper.
The dorsal surface with papillae; ventral surface with pedicels. The tables
have long spire of 4 rods, and 3 to 5 transverse beams. Habitat: Bohol, in 6 to 8
‘fathoms.
63. Holothuria impatiens Forskal.
Color in alcohol, light brown, inclined to violet. Integuments rough, the
smooth disks of the tables are pierced with 9 holes of equal size; buttons sym-
metrical with 6 holes. Habitat: Philippines, in 6 fathoms.
64. Holothuria scabra Jeger.
The color varies with different localities. Some are cinereous with almost
black transverse bands, with a few small whitish bands or spots on the back, the
belly being yollowish-white, and each papilla being surrounded with a small dark
circle. In other localities they are paler and punctated with a few large dark
spots, but are without the dark bands. The tables are solid, with smooth, well
developed disks, spires of usual shape with 12 to 16 teeth. The buttons have 6
holes, are symmetrical, and for the most part knotted. Habitat: Bohol, in shallow
water. Length 170 millimeters.
FISHERY RESOURCES OF THE PHILIPPINE ISLANDS. oud
65. Holothuria albiventer Semper.
Belly dirty gray, finely punctated; papille whitish; back dusky; tentacles
yellowish-white. The tables have large rounded disk with numerous small holes.
The spire is formed by 6 or 10 rods, its large rounded top is covered with small
teeth; buttons oval. Habitat: Bohol, in shallow water.
66. Holothuria squamifera Semper.
Papille seale-like. Tables small, numerous; spire long narrow, with 5 trans-
verse beams; buttons with from 6 to 12 holes. Habitat: Philippines.
THE MOST IMPORTANT WORKS RELATING TO TREPANG.
Semper, C. Reisen im Archipel der Philippinen (1868), 1, pt. 2.
THEEL, H. Report of the Scientific Results of the Exploring Voyage of H. M. S.
Challenger, 1873-76. Zoology (1882), 4, pt. 3; (1886), 14, pt. 2.
Pearsons, J. Report on the Holothurioide of the Gulf of Manaar. In Ceylon
Pearl Oyster Report. Roy. Soc. Supp. Rep. No. 5 (1903), 1, 181.
Smovmonps, V. Commercial Products of the Sea. New York (1879).
Mirsukuri, K. Notes on the Habits and Life-History of Stichopus japonicus
Selenka, Annot. Zool. Jap. (1903-1906), 5, 1.
Mirsuxuri, K. On Changes which are found with Advancing Age in the Calca-
reous Deposits of Stichopus japonicus, Selenka. Ibid. (1897), 1, 31.
Sturrer, C. Fauna des Java-Meeres. Nat. Tidj. v. Ned. Indie (1887), 47.
SenpnKka, E. Zeit. f. wiss. Zool. (1867), 17, 291.
Bett, F. J. Zoological Collection of H. M. S. ‘Alert.’ (1884).
Epwarps, C. L. Variation, Development and Growth in Holothuria floridana Pour-
talés and in Holothuria atra Jiger. Biometrika (1908), 6, 236-301.
Lak een
Lae
MBH
, F oy iy
ES ‘ a . 1 yd UAT aR 2
$
v 1a
; ME Rice de
rey, 2
Ne de® Ci
a H h dra? Wart hy
vy ah ih)
Mie i a eh ri pth
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}
ry
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;
me
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i
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s
ILLUSTRATIONS.
PLATE [. PHILIPPINE TREPANG.
Fie. 1. The oe.
2. The gan sim.
. The bark sim.
. The moi whar che.
. The hong che.
Om oo
PLATE II. DIFFERENT VARIETIES OF “BARK SIM.’
(Third grade Philippine Trepang. )
Fie. 1, Small black trepang.
. White ringed trepang.
. Yellowish brown trepang.
Dark brown trepang.
. Convoluted trepang.
. Small convoluted trepang.
Dom wD
Puate II]. PHILIPPINE SHARK-FIN.
Fie. 1. Dried shark-fin prepared for export.
2. The fin prepared for soup.
Prate [V. THREE VARIETIES OF SEA TURTLES.
Ite. 1. The loggerhead (Thalassochelys caretta Linn.).
2. Head of the loggerhead turtle.
3. The hawksbill turtle (Chelone imbricata Linn.).
4. Head of hawksbill turtle.
5. The green turtle (Chelone mydas Linn.).
6. Head of green turtle.
PLATE V.. PHILIPPINE TORTOISE-SHELL.
Fre. 1. Plate from the hawksbill turtle.
1
2. Section showing thickness of the above plate.
3. Plate from the green turtle.
4. Section showing thickness of the green turtle shell.
Prats VI. Comps MADE IN MANILA FROM PHILIPPINE TORTOISE-SHELL.
PuaAtE VII. PHILIPPINE WINDOW-SHELL.
lig. 1. Cross-section of shell near the adductor muscle showing actual width of
shell including the animal. ;
2. Window shell, with growth of crustacean ege's near one margin.
. Window shell opened and with the mantle of left side removed showing
the organs in place.
Pirate VIII. ANATOMY OF THE WINDOW-SHELL MoLuusk. «a, Mantle; 6, pallial
fringe; c, gills; d, adductor muscle; e, liver; /, genital lobe; g, foot:
h, anal funnel; 7, labial palps; 7, ventricle; /, auricle; /, kidneys.
319
oo
320 SEALE.
Prate IX. Urmizine Wrxpow SHELL.
Fic, 1. Shell window in the new General Hospital, Manila.
2. Sereen made of window shell and red narra wood.
PLATE X. SHELL LAMPS.
1. Small porch-light made from window shell.
2. Lantern light made from window shell.
3. Reading lamp made of wood and window shell.
4. The nautilus reading light. a, Base of red cement; b, stem of red coral-
line; e, shade of chambered nautilus; d, electric wire to bulb which is
hidden in nautilus shell. aig Secor aa
PratTeE XI. THE Top SHELL.
Fic. 1. Top shell (Yrochus niloticus Linn.). Showing cuts for buttons in the
partition walls.
2. Side view of Trochus niloticus Linn.
3. Trochus niloticus cut through the vertical plane.
4. Top view of Trochus niloticus Linn.
PrLaTe XII. THe TurBon SHELL.
Fic. 1. Turbon shell (Yurbo marmoratus Linn.)
. Turbon shell (young).
. Turbon shell cut on a vertical plane.
. Side view of Turbo marmoratus Linn.
pm Oo DO
SEALE : FISHERY RESOURCES OF THE PHILIPPINES. |
| Fig. 3.
[PxHin. Journ. Sct., Vou. VI, No.
Fig. 5.
PLATE I.
-
F
hes:
Was
pale tore
SEALE: FISHERY RESOURCES OF THE PHILIPPINES. ]
[PHIn. JouRN. Scr., VoL. VI, No.
Fig. 1.
Fig. 5.
Fig. 6.
PLATE II,
;
’ ~
t
i
ae 4
s
.
. JouRN. Scr., Vou. VI, No.
‘T Bl
‘9 ON ‘TA “TOA “10g ‘NUDOr TIHg]
[‘SANIddIIIHg FHL JO sHOUNOSTY AVAHSTY : AIvaS
‘TA "I0A “ICS ‘NUNOLF 11g]
"A S41Vv1d
HililitflihihlitAl
“WD ¢|
[(SANIdd ITH AHL oO SHOUNOSHY AVGHST AY : aTVWaAS
SEALE : FISHERY RESOURCES OF THE PHILIPPINES. | [PHIL. Journ. Sct., Vou. VI, No. 6.
Fig. 1.
15 cm.
EAE || | vk [|| al
PLATE vi.
SBALE : FISHERY RESOURCES OF THE PHILIPPINES. | [ PHIL. JouRN. Scr., Vou. VI, No.
OOO TUCURETUUODD
PLATE VII.
SEALE: FisHEeRY RESOURCES OF THE PHILIPPINES. ] [PHrn. JouRN. Sct., Vou. VI, No. 6.
PLATE VIII.
‘IT ‘Sl4
h. @eeeee
— ERSESR
EEESEE L we
SRekee ‘<
BESS Ss:
‘9 ON ‘IA “LOA “L § NUDOL TIN] [SANT4a1T1 TH FO SOOMNOSAQT UIMEST A : FIVaS
‘9 ‘ON ‘IA “IOA “IOS "NUNOL “T1Hg] [ SANIddIMHg FHL JO SAOUNOSTY AUAHSIY : ATVAS
SEALE : FISHERY RESOURCES OF THE PHILIPPINES. ] [PHIL. JourN. Sci., Vou. VI, No. 6
Fig. 1.
Fig 2.
WO SI
Width
PLATE XI.
SeaLeE: FISHERY RESOURCES OF THE PHILIPPINES. | [Putn. Journ. Scr., Vou. VI, Ne. 6.
Fig. 1.
Fig. 3.
Fig. 4.
TEEPE pepe
PLATE XII.
MILLER : NON-CHRISTIANS OF AMBOS CAMARINES | [Put.. Journ. Sct., Vou. VI, No. 6.
rileh Fig. 4.
PLATE I.
fea
yj
By
eee
“a
MILLER : NON-CHRISTIANS OF AMBOS CAMARINES. |
(PHIL. JourRN. Scr., Vou. VI, No. 6
MILLER : Non-CHRISTIANS OF AMBOS CAMARINES. | [PHin. Journ. Sct., Vou. VI, No. 6.
nN:
Fig. 1.
‘9 ON ‘IA “IOA “IOS “NUNOL TING] ['SUNIMVNVD SOdINY TO SNVILSIUHD-NON : YaTTIPY
THE PHILIPPINE JOURNAL OF SCIENCE,
D. General Biology, Ethnology and Anthropology.
Vol. VI, No. 6, December, 1911.
THE NON-CHRISTIAN PEOPLE OF AMBOS CAMARINES.
By Merron L. MInzer.
. (From the Division of Hthnology, Bureau of Science, Manila, P. I,)
The Province of Ambos Camarines is occupied mainly by the Bikol
people. In the northern part of Camarines Norte there are certain
towns which are occupied wholly or in part by Tagalogs. Many of the
latter are said to have come in from the north at the time of the dis-
covery of gold at Paracale and neighboring towns. With these excep-
tions all the municipalities of the province are occupied by Bikols.
However in the hills of both Camarines Sur and Camarines Norte there
are other people who apparently are neither Tagalog nor Bikol, In
Camarines Sur these people know themselves and are known to the
Christian population of the towns as “Agta.” The great body of them
lives on the slopes of the two extinct volcanoes, Iriga and Isarog. They
state that in Spanish times white people never ventured among them.
Their hostility toward the Spaniards is said to have been due to con-
tinual attacks made on them by the latter and to the consequent: desire
for revenge awakened in the hill people. To all appearances there
is no danger whatever in going alone among them at the present time.
Those about Mount Isarog are found for the most part about one-
third of the way up the slopes and apparently in about the place where
they have lived for years. ‘They formerly were scattered about in the
hills, but now are slowly coming to live in groups, although they say they
prefer to live scattered about. This is probably partly because they are
thus enabled to be nearer to their growing crops and partly because they
haye been accustomed to this method of life for many years.
The people of Consosep are typical of these groups of Isarog people.
Consosep is some six or seven hours travel from Mabatobato, almost
all of it uphill. Mabatobato is a barrio distant about three and one-
half hours from Pili. .A schoolhouse is located at Consosep on a
spur which juts out from Isarog and is perhaps 610 meters high. The
building can be seen for many miles, as the country immediately around
it is not wooded. A few hundred yards back of the schoolhouse toward
321
Bee MILLER.
the mountain are two houses. About the same distance below at a
place where the hill is a little less steep is a group of six small houses.
Off on another spur, across a deep gulch twenty minutes walk away,
can be seen another house. Still others are scattered about in the
forest, some near and some several hours’ travel away.
The day I was at Consosep about 75 individuals—men, women, and
children—came together in response to a call and they were probably
not more than one-half or two-thirds of all the people belonging to
this settlement. They are a peculiar people. They are not Negritos,
although the name by which they are known both among themselves
and to others—Agta—might indicate that they are. Neither are they
typically Malayan. ‘There are, it is true, many among them who do
not differ at all in appearance from the ordinary Christian Filipino,
but as a rule they are smaller than the average among the latter. They
are also darker. Very few of them have straight hair. Some have
hair which is almost kinky, while the majority have wavy hair. Some
have thick lips and a few the large, noticeable eyes of the typical Negro.
(Plate I, figs. 1 and 2; Plate III.)
They dress like most of the other people of the Philippines. The
women wear a camisa and for a skirt several pieces of cloth wrapped
about the body and tucked in at the waist. The men wear trousers
reaching to the knees and most of them some kind of a jacket or shirt.
However, when working in the fields they wear usually only the loin
cloth. i
In former times these people lived in rude shelters much like those
in which the Negritos still live. Now they dwell in small houses, so
small that even they can not stand upright anywhere in them. They
are built about 1.5 meters above the ground with floors of bamboo and roofs
of leaves.
These people plant upland rice, camotes, maize, taro, squash, bananas,
yams, and some few other plants. They have no goats or sheep, but
occasionally kill birds to eat.
An old woman with whom I talked who had lived at Consosep all
her life said that she did not remember a time when there were Negritos
about there. From this as well as from the appearance of the people
one would conclude that the Negrito admixture took place many years
ago. She also said that formerly they were more numerous than now,
that they had been killed by smallpox, cholera, and in fights with the
Spaniards, but that they were increasing in number now.
They marry at from 13 to 15 years of age. The old woman above
mentioned told me of one woman who had eight children. One man
sometimes has as many as three wives, although as a rule they are mo-
nogamous. They are said to have a language of their own which has
NON-CHRISTIANS PEOPLE OF AMBOS CAMARINES. Be
some Bikol words in it. It may be, however, that this is merely a
dialectic variation of Bikol and not a distinct language.
On the Kalawat Islands, which lie a few miles east of Paracale in
Camarines Norte, there is a small population most of whom are Bikol,
like the people on the mainland opposite, but there are besides the
Bikols certain small groups of people known as “Dumagat.” They
live for the most part in small groups by themselves not far from the
Bikol settlements. These people too, like the Agta of Camarines Sur,
show evidence of Negrito blood. They are darker than their Bikol
neighbors though not noticeably smaller. Some of them have wavy
and some curly hair while others have hair as straight as the ordinary
Filipino. (Plate I, figs. 3 and 4.)
The Dumagat people of Kaboong Island, one of the Kalawat group,
said they came from the mainland. One man was from near Nueva
Caceres and looked much like the people about Mount Isarog. They
said that they had all been baptized, but the probability is that they
are practically non-Christians, as they are remote from any Christian
influence. They talk Bikol among themselves, live for the most part
scattered about on the hillsides in houses like those of other Filipinos,
plant camotes, maize, taro, and yams, but do not plant rice. They
had never heard of Negritos living on the Kalawat Islands. They say
they call themselves Dumagat because they live near the sea.
I was told that on Butawanan Island off Kinabugsukan Point in
Camarines Sur there is a considerable number of these Dumagat people.
There are also a few of them scattered among the Bikol people of the
coast towns. I did not visit Butawanan and so can not say whether
the people of that island resemble the Dumagat of the Kalawat Islands.
There are three possible explanations of the origin both of the Agta
people in the vicinity of Mounts Isarog and Iriga, and of the Dumagat of
the Islands off the east coast of the province and of the neighboring
shores of the mainland. The resemblance between the two groups is
sufficiently close to lead one to believe that their origin may be the same.
The first possibility is that they are remnants of an earlier Malayan
invasion which preceded that which brought the Bikols and Tagalogs
to the Philippines. The second is that they are the result of crossing
between an aboriginal Negrito population and their Malayan neighbors.
It is furthermore possible that they may be the result of the crossing
of some primitive Malayans with Negritos. That there is Negrito
blood in them I have no doubt, although this opinion is based only
on their physical appearance.
The simplest explanation of the characteristics of these people is
that they are the result of crossing many years ago between the Ma-
layan people and Negritos. Occasionally even now men from the low-
324 MILLER.
lands join these hill people, preferring the life of the latter. to that
of their fellows in the plains.
The Negritos in Camarines are to be found both in Camarines Sur
and Camarines Norte. In Camarines Sur a few Negritos live near
Payatan on the slope of Mount Isarog. Here scattered about they
dwell in rude shelters in the forests. They work for their Filipino
neighbors. They are typical Negritos, apparently without admixture
of other blood.
Near the town of: Iriga there is a settlement of about 68 people of
mixed Negrito and Malayan blood. Some have almost kinky hair and
others hair almost straight. I saw no one at this settlement who ap-
peared to be of pure Negrito blood, although in Iriga itself are some
10 or 15 Negritos who are said to be practically slaves and who are
not allowed to leave their masters. They do, however, occasionally escape.
In Camarines Norte on the other hand are many pure Negritos,
although how many I am unable to say. ‘There is one groupinear the
barrio of Batobelani and there is at least one other group near Ragay
on the west coast of Camarines. These Negritos do a little farming
on their own account, but they more often work for the Christian Fili-
pinos planting and harvesting crops. When they come into the Christian
settlements the women and some of the men wear the ordinary Filipino
costume. Others of the men wear only the customary loin cloth. The
shelters in which they live are often the simplest possible, consisting
of a rough floor and a roof of leaves. (Plates II, IV, V.)
It seems to be a rare thing with them to intermarry with the Christian
Filipino. All whom I saw in Camarines Norte looked like pure Negri-
tos with no admixture of other blood. Im all probability prejudice
against marriage with the Negritos has increased with the coming of
Christianity. If this be true most of the blending of the Negrito and
Filipino blood which has occurred here took place many years ago.
There are probably several hundred Negritos in Camarines Norte.
I suspect most of them have come to be dependent to some extent on
the Christian Filipinos and, therefore, live near them. They are a
mild-mannered, inoffensive people, but I did not see enough of them
to learn much about their mode of life.
They are typical Negritos. They are short of stature, have dark
skin, closely curled hair, and flat noses. When they are of pure blood
there is never any possibility in the Philippines of sauces them
for any other people.
With the exception of the Negritos, the Dumagat people, and those
living about Mounts Isarog and Iriga all the other inhabitants of
Camarines I believe to be Bikol, with some Tagalogs in the north and
a few individuals from other parts of the Philippines scattered about
here and there.
ILLUSTRATIONS.
PLATE I.
Fie. 1. Woman of Consosep, Camarines, showing no evidence of Negrito blood.
2. Man of Consosep, Camarines, showing strong evidence of Negrito blood.
3 and 4. Men of Kalawat Islands, Camarines, showing traces of Negrito blood.
PLATE II.
Figs. 1 and 2. Negrito women, near Ragay, Camarines.
Fie. 3. Negrito man, near Ragay, Camarines.
4. Negrito man, near Batobelani, Camarines.
Puate IIT.
Fic. 1. Group of men, near Mount Iviga, Camarines. Some evidently have
Negrito blood; others not.
2. Negrito hut near Mount Isarog, Camarines.
Puate LV.
Group of Negrito men, women. and children; Ragay, Camarines.
> 2 b= beer?
ses
wey
THE PHILIPPINE JOURNAL OF SCIENCE,
D. General Biology, Ethnology and Anthropology.
Vol. VI, No. 6, December, 1911.
THE STRUCTURE OF THE PALLIAL TENTACLES OF LIMA
SPECIES:
By LAWRENCE E. GRIFFIN.’
(From the Zoélogical Laboratory, University of the Philippines.)
While turning over stones on a coral reef on the eastern coast of
Negros, P. I., there came from under one which I lifted a small Lima
which went flapping off, like
a startled Pecten, in a des-
perate effort to escape.
From the edges of the man-
tle trailed scores of delicate
tentacles, from 25 to 60 mil-
limeters in length, of a
blood-red color. As quickly
as possible I caught the little
creature and immediately
several dozen of the tentacles
fastened to my hand. Many
of them clung so tightly that
they were broken before
letting go.
Each of the tenta-
cles was ringed with an-
nual grooves. These an-
nulations and the great
adhesive power of the
tentacles, which seemed
to be due more to suc-
tion than to a mucila-
ginous secretion, were
immediate reminders of
the tentacular cirri of
Nautilus. This first
specimen of Lima sp. was destroyed by an accident and it was several
months before more were found. These were discovered buried at a depth
Fig. 2.
* Associate professor of zodlogy, University of the Philippines, Manila, P. I.
327
28 PALLIAL TENTACLES OF LIMA.
wo
of 8 to 10 centimeters in the loose broken coral on the inner side of a
reef.
A microscopic examination proved that the internal structure of the
tentacles of this bivalve is even more remarkably like that of the Nautilus
cirri than the external structure. A cross sec-
tion (fig. 1) shows a large nerve extending
through the center of the tentacle; radial
muscles pass from the central region to all parts
of the periphery; and strong longitudinal mus-
cles lie in the spaces between the radial fas-
ciculi. The central portion of the nerve is com-
posed exclusively of fibers. Upon its surface
is an almost continuous layer of nerve cells, but
more or less distinct aggregations of nerve cells
are found at poimts corresponding to the an-
nular ridges of the surface of the tentacle.
As in the Nawtilus cirri,
the epidermal cells are high
upon the ridges but very low
in the grooves of the ten-
tacle (fig. 3). On the outer
surface of the tentacle is a
narrow longitudinal groove.
at the base of which also the
epidermal cells are very low
(fig. 1). In some cases the
epidermal cells were found to
be crowded with mucous se-
cretion. i
The muscular develop-
ment of the Nautilus cirri is
greater, and there is more
difference in the epidermis of
the inner and outer stirfaces
than appears in the tentacles
of Lima, but in the charac-
teristic structures of the ten-
_tacles the differences are
those of degree rather than of kind. - The striking parallelism of develop-
ment of these rather complex structures in forms so widely separated.
systematically, is the more interesting when we remember that the ten-
tacles of Lima are appendages of the mantle edge, while those of Naw-
tilus hélong to the head or foot.
ILLUSTRATIONS.
TEXT FIGURES.
Fie. 1. Transverse section of a tentacle of Lima sp. Im, longitudinal muscle
bundles; ”, nerve; 7m, radial muscles. Original.
2. Transverse section of a cerus of Nautilus pompilius. A, artery; CU,
circular muscle layer; H, thickened epithelium on inner surface; LM,
LM’, longitudinal muscles; N, nerve; OM, oblique muscle layer; RM,
Tadial muscles; 7'’M, transverse or radial muscles; V, vein. (From
Griffin, Anatomy of Nautilus pompilius. )
3. Longitudinal section of a pallial tentacle of Lima sp. Original.
4. Longitudinal section of the tip of a cirrus of Nautilus pompilius. (From
Griffin, Anatomy of Nautilus pompilius. )
329
Apri: Pea aon
ae oy
ESA ieci ty
Ce eas iy age ae ih he,
THE PHILIPPINE JOURNAL OF SCIENCE,
D. General Biology, Ethnology and Anthropology.
Vol. VI, No. 6, December, 1911.
BEITRAG ZUR COLEOPTEREN FAUNA DER PHILIPPINEN.
= Von J. Moser.
(Berlin, Germany.)
Holotrichia latecostata sp. nov.
Supra picea, pruinosa, subtus brunnea, nitida, pygidio abdomineque
flavis. Capite fortiter subrugoso-punctato clypeo margine antico emar-
ginato; prothorace lato, lateribus medio rotundato-dilatatis, disco spar-
sim, versus margines laterales paulo densius punctato, linea media laevi,
antice abbreviata ; scutello remote punctato, medio laevi; elytris, singulo
4-costato, costa prima postice ad suturam versus valde dilatata, subrugoso-
punctatis,~feminae juxta suturam transversim-plicatis; pygidio haud
dense umbilicato-punctato. _ Subtus medio subtiliter parce punctato, late-
ribus densius punctatis et flavo-pilosis; tibiis anticis tridentatis, articulo
primo tarsorum posticorum secundo aequali.
Long. 16 mill.
Typus No. 11739 in Coll. Ent., Bureau of Science, Manila, P. I.
Hab: Panawan, Bacuit (C. MW. Weber, Collector).
Die Form des Halsschildes, die pruindse Oberseite und der aufgetrie-
bene gelbe Bauch verweisen die Art in die mucida-Gruppe. Der Kopf
ist kraftig, fast runzelig punktiert, der Clypeus in der Mitte leicht aus-
gebuchtet. Die Seiten des Halsschildes sind in der Mitte bogenformig
erweitert, vor den Vorderecken ist der Seitenrand flach ausgebuchtet.
Die Oberfliche ist zerstreut mit Nabelpunkten bedeckt, doch stehen die
Punkte nach den Seiten zu etwas dichter und sind grober. Hine punkt-
freie Mittellinie ist nur in der hinteren Hilfte zu erkennen. Das Schild-
chen ist zerstreut punktiert, seine Mitte glatt. Die Fliigeldecken sind
miassig dicht nabelartig und namentlich beim ? etwas runzelig punktiert.
In der Mitte neben der Naht zeigen sich beim ? Querfalten. Jede
Pliigeldecke lasst 4 schwache Rippen erkennen, von denen die innerste
sich hinten sehr stark nach der Naht zu verbreitert. Wahrend bei dem
yorliegenden ¢ die ganze Oberseite der Fltigeldecken pruinés ist, sind
bei den beiden 2 die Seiten glinzend. Das Pygidium ist schwach gewolbt
106346——4 331
332 MOSER.
und miassig dicht mit Nabelpunkten bedeckt. Die Unterseite ist mit
Ausnahme des gelben Abdomens braun, in der Mitte sehr zerstreut, an
den Seiten dichter punktiert und hier behaart. Die behaarten Stellen
an den Seiten des Abdomens sind matt. Die Vorderschienen sind in
beiden Geschlechtern kriftig dreizihnig, die beiden ersten Glieder der
Hintertarsen sind gleich lang. Die Krallen sind an der Basis ver-
breitert, am Ende ziemlich stark gebogen, der mittlere Zahn ist schwach
und etwas nach riickwarts gerichtet.
Protaetia banksi sp. nov.
Viridis, flavo-maculata, supra opaca, subtus nitida. Capite maris sub-
tiliter, feminae grosse punctato, fronte 2- an 4-flavo-maculata, clypeo
nitido, marginibus paulo elevatis, margine antico emarginato ; prothorace
lateribus flavo-marginatis, vitta marginali postice abbreviata, disco flayvo-
bimaculato; scutello immaculato ; elytris obsolete punctato-striatis, juxta
scutelli basin atque apicem, prope suturam, apice, juxta margines laterales
et inter scutellum et humerum maculis flavis ornatis; pygidio flavo-bivit-
tato, vittis antice furcatis. Subtus pectoris abdominisque lateribus flayo-
maculatis ; procéssu mesosternali dilatato, margine antico rotundato ; tibiis
anticis in utroque sexu tridentatis, mediis et posticis intus flavo-ciliatis.
Long. 17 mill. .
Typus No. 6334 in Coll. Ent. Bureau of Science, Manila, P. I.
Hab: Negros Occidental, Bago (Charles S. Banks, Collector).
Die Art hat in der Zeichnung Ahnlichkeit mit venerabilis Mohn.
Sie ist etwas kleiner, die Unterseite ist bei allen vorliegenden Hxem-
plaren griin und auf den Fliigeldecken befindet sich unterhalb der Schul-
ter eine schmale gelbe Seitenrandbinde, die bei venerabilis fehlt. Auch
der Forceps ist anders gebildet wie bei dieser Art. Der Clypeus ist
beim ¢ fein, beim ? kraftig punktiert, missig hoch umrandet, der Vor-
derrand ausgebuchtet. Auf der Stir befinden sich 2 oder 4 gelbliche
Tomentflecken. Das Halsschild lisst infolge der Tomentbekleidung eine
Skulptur nicht erkennen. Die Seitenrinder sind gelb gesaumt, doch
-reicht die Seitenrandbinde nicht bis zu den Hinterecken. Auf dem Dis-
cus befinden sich 2 rundliche gelbe Makeln. Das Schildchen ist unpunk-
tiert und ungefleckt. Die Schulterblatter haben einen hinteren gelben
Rand. Die Fliigeldecken lassen nur undeutliche Punktreihen erkennen.
Sie sind neben der Naht etwas verflacht, so dass die Naht deutlich her-
yortritt. Von gelblicheln Makeln befinden sich auf ihnen je einer neben
Schildchenbasis und Schildchenspitze, ein rundlicher in der Mitte und
ein querer hinter der Mitte neben der Naht, ein klemer an der Naht-
spitze. Neben dem Seitenrande lauft eine schmale Lingsbinde unter-
halb der Schulter und befinden sich dahinter 4 mehr oder weniger quere
Makeln, von denen der letzte neben dem Endbuckel liegt. Ausserdem
befinden sich hinter dem Vorderrande noch 2 kleine, hintereinander-
CELEOPTEREN FAUNA DER PHILIPPINEN. 333
liegende Flecken. Das Pygidium tragt jederseits eine gelbliche Langs-
binde, welche sich nach vorn verbreitert und gabelt. Auf der Unter-
seite sind die Seiten yon Brust und Abdomen gelb gemakelt und zwar
tragt jedes Abdominalsegment jederseits 2 gelbe Querbinden, die aus-
sere am Hinterrande, die innere am Vorderrande. Der Brustfortsatz
ist nach vorn yerbreitert, sem WVorderrand ist flach abgerundet, seine
Oberfliiche fast glatt. Die Vorderschienen sind in beiden Geschlechtern
dreizihnig, die Vorderhiiften, Schenkel und Schienen sind gelb bewimpert.
Ich widme die Art dem Entdecker derselben, Herrn Charles S. Banks,
Entomologist, Bureau of Science in Manila.
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INDEX.
(New names are printed in heavy-faced type; numbers in italics indicate synonyms or
references of minor importance.)
Be A
A-amiid, 282.
A-apox di gimaiyang, 240.
Ablabes philippinus Boettger, 261.
tricolor (Schlegel), 261.
Acrochordine, 255.
Actinocyclira, 61.
JBtheopsar, digestive system in, 32.
‘Athopyga bonita Bourns and Worcester, 46.
magnifica Sharpe, 46.
Agar-agar, 309,
Aghardhiella sp., 309.
Agongs, value of, 130.
Aipysurus eydouxii (Gray), 265.
Aktinocyclina, 67.
Alang, 82.
Allin, Benjamin Casey: Allin’s Standard
English-Visayan Dictionary, reviewed,
281.
Alveolina, 61.
Alveolinella, 54, 56, 76.
quoyi, 55.
Amblycephalide, 267.
Ambos Camarines, non-Christians of, 321.
Amphistegina cf. mamillata d’Orb., 75, 77.
niasi Verbeek, 67, 75.
Anas, digestive system in, 32.
Anous stolidus (Linnzus), 171.
Anthropology. The men of Cainta, 7; Fi-
lipino ears: III. Negrito, 107.
Anthus rufulus (Vieillot), 46.
Antipatharia sp., 307.
Aragan, 309.
Artamides panayensis Steere, 43.
Asterocyclina, 61.
Astur trivirgatus (Temminck), 41.
Augang, 83.
B
Bagobos of Davao Gulf, 127.
Bagol, 82, 233.
Baipandi, 133.
Bakayauan, 97.
Baki, 82, 233, 236.
Balakat, 134.
Balatan, 283.
Balatik, 134.
Balitok, 81.
Balu, 234.
Bangibang, 232.
| BARTON,
Baris-baris, 309.
Bark sim, 284.
ROY FRANKLIN,
Feast of the Kiangan Ifugao,
also BEYER, H. OTLEY,
The Harvest
81. See
| Basi, 83.
Baya, 83.
BEAN, ROBERT BENNETT, Filipino Ears:
III. Negrito, 107; The Racial Anatomy of
the Philippine Islanders, reviewed, 223.
BEAN, ROBERT BENNETT, and PLANTA,
FEDERICO S., The Men of Cainta, 7.
| Béche de mer, 283.
BEYER, H. OTLEY, Review of Bean’s The
Racial Anatomy of the Philippine Island-
ers, 223.
BEYER, H. OTLEY, and BARTON, ROY
FRANKLIN, An Ifugao Burial Ceremony,
227.
Bilate, 283.
Bilau, 231.
Binabudan,
Binadayan, 83.
Birds from northern Negros, 39.
Birds, Philippine sea, newly discovered breed-
ing places of, 167.
Bischofia javanica Bl., 244.
Black coral, 307.
Blue coral, 307.
Boide, 255.
Boiga angulata (Peters), 263.
cyonodon (Boie), 264.
’ dendrophila (Boie), 263.
philippina (Peters), 263.
83.
| Boigine, 263.
Boobies, hybridism among, 179.
Book reviews.. See REVIEWS.
Borkenkafer der Philippinen, 17.
Bradypus, 155.
Bubad, 236.
Bubud jars, 83.
Bubulcus coromandus (Boddaert), 41.
Bubulcus, digestive system in, 32.
Buga, 84.
Bugan, 81, 96.
Bulolo, 302.
Buluhan, 95.
Burial ceremony, Ifugao, 227.
Burial jars, 3.
Butek, 82.
335
336
Cc
Cacomantis merulinus (Scopoli), 42.
Cainta, men of, 7.
Calamaria bitorques Peters, 262.
everetti Boulenger, 262.
gervaisii Duméril et Bibron, 262.
grayi Giinther, 262.
mearnsi Stejneger, 262.
mindorensis Boulenger, 262.
Callisitta cnochlamys (Sharpe), 45.
Camiguin Island, burial mounds of, 1; loca-
tion and description of, 1.
Canot-canot, 309.
Catfish, 310.
Cauat-cauat, 309.
Cave burials, 3.
Cayman skin, 310.
Centetes, 193.
Ceyx bournsi Steere, 41.
Chaetomorpha crassa (Ag.) Kiitz., 309.
Chambered nautilus 301, 303.
Chelone imbricata Linn., 291.
mydas Linn., 292.
Chersydrus granulatus (Schneider),
311.
Chiloscyllium indicum Linn., 312.
Chirodota dubia Semper, 313.
incongrua Semper, 313.
panaensis Semper, 314.
rigida Semper, 313.
yariabilis Semper, 313.
Cholepus, 155.
Chrysochloris, 187, 193.
Chrysocolaptes xanthocephalus Walden and
Layard, 42.
Chrysopelea ornata (Shaw), 264.
Cibolan, 132.
Cinnyris guimarasensis Steere, 46.
Cittocincla nigrorum Grant, 44.
Coccotrypes graniceps Hichhoff, 21.
pygmeus Eichhoff, 17.
Cocos nucifera Linn., 25.
Codium tenue Kiitz., 309.
COLE, FAY COOPER, The
Davao Gulf, 127.
Coleopteren Fauna der Philippinen, 331.
Colochirus anceps Selenka, 315.
ceruleus Semper, 314.
ecucumis Semper, 314.
eylindricus Semper, 315.
quadrangularis Less., 315.
quadrangulus Less., 286.
tuberculosus Quoy and Gaim.,
315.
viridis Semper, 314.
Colubride, 255. |
Colubrine, 256. \
Colugo, 148.
Columba griseogularis (Walden and Layard),
41.
Conic shell, 301.
Coral, black, 307. }
blue, 307. |
Japanese precious, 305. |
precious, 305.
red organ-pipe, 307.
255,
Bagobos of
INDEX.
| Corallium boshuensis Kishinouye, 303.
confusum Moroff, 306.
elatius Ridley, 306.
inutile Kishinouye, 306.
japonicum Kishinouye, 305, 306.
johnsoni (Gray), 306.
konojoi Kiskinouye, 306.
maderense (Johnson), 306,
nobilis Pallas, 305.
pusillum Kishinouye, 306.
regine (Hickson), 306.
rubrum Linn., 305.
secundum (Dana), 306.
stylasteroides (Ridley), 306.
sulcatum Kishinouye, 306.
Corals, reef, 307.
Cordyline terminalis Kunth, 235.
Cotton-spinner, 283.
Craniorrhinus waldeni Sharpe, 42.
Crimes, 131, 132.
Criollas, 7.
Crocodile skin, 310.
Crocodilus palustris Lesson, 310.
porosus Schneider, 310.
Crossotarsus comatus Chapuis, 26.
lecontei Chap., 17.
Crotaline, 267.
Cryphalus squamulosus Strohmeyer, 20.
Cryptolopha oliyacea (Moseley), 43.
Cucumaria canescens Semper, 313.
citrea Semper, 312.
conjungens Semper, 312.
longipeda Semper, 312.
maculata Semper, 312.
mirabilis Théel, 313.
versicolor Semper, 312.
CURL, HOLTON C., Notes on the Digestive
System of Hydrocorax, 31.
Cyanomyias celestis (Tweeddale),
Cycloclypeus, 64.
Cycloclypeus communis Martin, 57, 60, 75,
TA TL
Cyclocorus lineatus (Reinhardt), 258.
Cynocephalus, 140, 186, 205.
D
Dactylipalpus quadratocollis Chapuis, 18.
transyersus Chapuis, 18.
Dangla, 235.
Dangoia, 244.
Darago, 133.
Dasycrotapha speciosa Tweeddale, 44.
Datilon, 240.
Daya, 88.
Dendrelaphis czruleatus Griffin, 261.
caudolineatus (Gray), 261.
fuliginosus Griffin, 261.
modestus Boulenger, 261.
terrificus (Peters), 261.
43.
| Dendrophis pictus (Gmelin), 259.
punctulata (Gray), 260.
Diczum dorsale Sharpe, 46.
hematostictum Sharpe, 46.
Dicrurus mirabilis Walden and Layard, 46.
Discocyclina, 61.
INDEX.
Disteira cincinnatii Van and
Thompson, 264.
cyanocincta (Daudin), 265.
fasciata (Schneider), 264.
longiceps (Giinther), 265.
ornata (Gray), 265.
semperi (Garman), 265.
spiralis (Shaw), 265.
Diwata, 133.
Doliophis bilineatus (Peters), 266.
philippinus (Giinther), 266.
Dolium costatum, 65.
Dotal, 83.
DOUVILLE, HENRI, Les Foraminiféres dans
le Tertiaire des Philippines, 53.
Dryocalamus philippinus Griffin, 259.
Dryophiops philippina Boulenger, 264.
Dryophis prasinus Boie, 264.
Denburgh
E
Ears, Filipino, 107. |
Ears, Negrito, 107.
Earth World, 88. |
Eccoptopterus sexspinosus Motsch, 25. |
Echinocucumis adversaria Semper, 313.
Edible seaweeds, 308. | ‘
Edible turtle, 295.
Edolisoma panayense Steere, 43.
Elaphe erythrura (Duméril et Bibron), 260.
oxycephala (Boie), 260.
philippina Griffin, 260.
Elapine, 265.
Enteromorpha intestinalis L., 309.
Entomology. Borkenkafer der Philippinen,
17; Beitrag zur Coleopteren Fauna der |
Philippinen, 331.
Epicrates inornatus (Reinhardt), 268. |
Erinaceus, 161, 193.
Ethnology. The burial mounds of Cami-
guin Island, 1; on a quinary notation |
among the Ilongots of northern Luzon, 47 ; |
the harvest feast of the Kiangan Ifugao, |
81; the Bagobos of Davao Gulf, 127;
an Ifugao burial ceremony, 227; the |
non-Christian people of Ambos Camarines,
321.
Eucheuma“spinosum (L.) J. Ag., 309.
Eugpamolak Manobo, 132.
Eulepidina, 59, 61, 68.
Eurydactylus multispinous, 25.
sexspinosus Motsch, 17, 25.
F
Feast of Kiangan Ifugao, harvest, 81.
Filipino ears, 107.
Fishery resources of the Philippines, 283.
Flabelliporus orbicularis Dervieux, 74.
Flying lemurs, Galeopteride, the skeleton
in the, 139, 185.
Foraminiféres dans le Tertiaire des Philip-
Pines, les, 53,
Fregata aquila (Linnzeus), 174.
Frog tadpoles, 219.
Fucus gulaman Blanco, 309.
G
Galeopithecus temminckii Wat., 148.
Galeopteride, the skeleton in, 139, 185.
Gamet, 309.
Gan sim, 284.
Gelidium, 309.
Gerardia prevostiana (Hydoux et Geryaise),
263.
Ginem, 134.
Globigerina, 77.
Gracillaria confervoides (L.) Grev., 309.
crassa Hary., 309.
eucheumoides Harv., 309.
lichenoides (L.) Grey., 309.
Great top shell, 301.
Green snail, 301.
Green snail shell, 302.
Green turtle, 292.
GRIFFIN, LAWRENCE EDMONDS, A
Check-list and Key of Philippine Snakes,
253; Review of Kofoid’s The Biological
Stations of Europe, 221; The Structure
of the Pallial Tentacles of Lima Species,
327.
Gulaman, 308.
Gungat, 238.
Guraman, 309.
Gymnura, 193.
H
Hagaga, 83.
Haganga, 83.
Halcyon moseleyi (Steere), 42.
Halupe, 232.
Halymenia formosa Hary., 309.
Hana’ti, 239.
Hapi, 234.
Haplodactyla molpadioides Semper, 313.
molpadioides pellucida Selenka,
318.
Haplonodon philippinensis Griffin, 258.
Haplopeltura boa (Boie), 267.
Harvest feast of the Kiangan Ifugao, $1.
Hawksbill turtle, 291.
Head-hunting, Ifugao, 228.
Heliopora ccerulea Linn., 307.
| Hemibungarus calligaster (Wiegmann), 266.
collaris (Schlegel), 266.
Hemiprocne major (Hartert), 42.
Herpetology. A check-list and key
Philippine snakes, 253.
of
| Heterostegina, 57.
Hierococcyx sparverioides (Vigors), 42.
Hinamar, 84.
Hipag, 247.
Hirundo gutturalis Scopoli, 43.
rustica Linneus, 43.
Hisam, 283.
Holarchus octolineatus (Schneider), 259.
phenochalinus (Cope), 259.
Hologerrum philippinum Giinther, 263.
Holothuria albiventer Semper, 317.
atra Jeger, 315.
coluber Semper, 316.
edulis Lesson, 316.
erineus Semper, 315.
Holothuria fusco-cinerea Jeger, 316.
graffei Semper, 315.
immobilis Semper, 316.
impatiens Forskal, 316.
marmorata Jeger, 315.
monacaria Lesson, 316.
pervicax Selenka, 315.
pulchella Selenka, 315.
scabra Jeger, 316.
similis Semper, 315.
squamifera Semper, 317.
tenuissima Semper, 315.
vagabunda Selenka, 316.
Holotrichia latecostata Moser, 331.
Homalopsine, 263.
Hong che, 285.
Hopea, 19, 20.
Human sacrifice, 130.
Humangali page, 83.
Hurria microlepis (Boulenger), 263.
rhynchops (Schneider), 263.
Hydrine, 264.
Hydrocorax hydrocorax, digestive system
of, 31.
Hyloterpe winchelli Bourns and Worcester,
45.
I
Idu, 236.
997
Ifugao burial ceremony, 227.
Ifugao, harvest feast of the Kiangan, 81.
Ilongots, quinary notation among, 47.
I-nab-ni-tan, 238.
Invertebrate zodlogy. On the habits
Thalassina anomala (Herbst), 213; the
structure of the pallial tentacles of Lima |
species, 327.
Iole guimarasensis Steere, 43.
Isinglass, 309.
J
Japanese precious coral, 305.
Johnius belengeri C. and V., 310.
K
Kadangyan, 81, 239.
Kanduli, 310.
Kapas, 296.
Kiangan Ifugao, harvest feast of,
Kilillo, 233.
Kittacincia superciliaris Bourns and Wor-
cester, 44.
Kofoid, Charles Atwood: The Biological
Stations of Europe, reviewed, 221.
Kolating, 81.
Koliaban, 98.
$1.
L
Lagod, 88.
Lalong, 302.
Langalang, 93.
Lapemis hardwickii Gray, 265, 311.
Laticauda colubrina (Schneider), 265.
laticaudata (Linneus), 265.
Lemur yolans Linn., 148.
of
INDEX.
Lemurs, the skeleton in the flying, 133, 185.
Lepidocyclina, 59, 60, 75.
andrewsiana, 63.
angularis Newton et Holland,
64, 68, 70.
var. angulosa, 68.
var. borneénsis, 68.
earteri Martin, 65, 69.
dilatata, 63, 65, 69, 78.
elephantina Mun. Chalm., 70.
ephippioides, 63.
ferreroi Provale, 67, 70, 73.
formosa Schlumberger, 63, 64,
66, 67, 70, 72, 76.
gallienii Lemoine
Douvillé, 65, 69.
gigantea Martin, 70.
inermis Douvillé, 72, 76.
var. inflata, 68.
inflata Provale, 70, 74.
insule-natalis Jones et Chap.,
62, 63, 67, 69, 71, 76, 78.
joffrei, 65.
mantelli, 65.
marginata Lem. et R. Douv.,
Th.
, martini, 64, 66.
meodispansa, 62.
morgani, 64, 65, 70.
= multipartita, 61.
murrayana, 63.
ebia kes
ngembaki Schlumberger, 63,
67, 70.
premarginata, 73, 75.
provalei Osimo, 67, 70.
raulini, 67.
richthofeni W. D. Smith, 71,
72, 16.
schlumbergeri, 67.
smithi Douvillé, 73, 75.
sumatrensis, 64, 67.
tournoueri Lem. et R. D.,
67, 68, 70.
tournoueri, var. inflata Pro-
vale, 74.
yerbeeki Newton et Holland,
62, 63, 64, 68, 70, 73, 77,
78. .
Leptophis vertebralis Duméril
268.
Leucotreron occipitalis (Bonaparte), 41.
Liagora cheyneana Harv., 309.
Lima species, pallial tentacles of, 327.
Linauwa, 81, 84.
Liu-lfua, 239.
Lock, 301.
Loggerhead, 292.
L6éhép, 233.
Loriculus regulus Souancé, 41.
Luzon, quinary notation among Ilongots of,
47.
et Bibron,
M
| Mabalian, 133.
Macrocelides, 193.
Magani, 133.
INDEX.
Magindanau, 129.
Makalun, 89.
Mamali, 310.
Mammalogy. The skeleton in the
lemurs, Galeopteride, 139, 185.
Manama, 129.
Manatus, 155.
Mandarangan, 133.
Mangikapia, 102.
Manojos, 82.
Marginopora, 56.
Marine products of the Philippines, 283.
Marriage ceremony, 135.
McGREGOR, RICHARD C., Notes on a Col- |
lection of Birds from Northern Negros,
39; Record of a Puffiinus New to Phil-
ippine Waters and Description of a New
Species of Micranous, 183.
Megalurus tweeddalei McGregor, 45.
Micranous leucocapillus (Gould), 173.
worcesteri McGregor, 173, 183.
MILLER, MERTON L., The Burial Mounds
of Camiguin Island, 1; review of Allin’s
Standard English-Visayan Dictionary,
281; The Non-Christian People of Ambos
Camarines, 321.
Miogypsina, 74, 77, 78..
Miogypsina irregularis Sacco, 74, 77. “
irregularis, race orientalis Dou-
villé, 74.
Miscasthus sinensis Audr., 231.
Moi whar che, 285.
Monamud, 87.
Monbakayauan, 97.
Monbaki, 102.
Monbuluhan, 95. ,
Monhu-aa, 99.
Monkoliaban, 98.
Monlagim, 99.
Monlana, 92.
Monlapu leaders, 86.
Monligid, 94.
Monmakalun, 89.
Montobal, 86.
Monwiwik, 98.
Morenos, 7.
MOSER, J., Beitrag zur Coleopteren Fauna
der Philippinen, 331.
Mounds of Camiguin Island, burial, 1.
Milleria lecanora Jeger, 313.
mauritiana Quoy and Gaim., 313.
nobilis Sel., 313.
-Munang, 283.
Mungamu-gaman, 241,
Munhimting ceremony, 229.
Munia jagori Martens, 46.
Munlapu, 237.
Mun-liu-liua, 240.
Muntbig, 236.
Muscadivores chalybura (Bonaparte), 41.
Myiogypsina, 57.
Myology. Notes on the digestive system of |
Hydrocorax, 31.
Mythology, Ifugao, 81.
flying
339
N
Naja bungarus Schlegel, 266.
naja (Linneus), 265.
naja var. ceca Gmelin, 266.
miolepsis Boulenger, 266, 268.
sputatrix Boie, 268.
samarensis (Peters), 266.
Natrix auriculata Gtinther, 257.
chrysarga Boie, 257.
crebripunctata (Wiegmann), 257.
dendrophiops (Gtinther), 257, 268.
lineata (Peters), 257.
spilogaster Boie, 257.
stolata (Linnzus), 257.
Nautilus, 327.
pompilius Linn., 301, 303.
Negrito ears, 107.
Negros, notes on birds from, 39.
Nephrolepidina, 59, 61, 62, 63, G8, 73, 75.
Netuma nasuta BI., 310.
Nguhu, 233.
Non-Christians of Ambos Camarines, 321.
Notation among Ilongots of northern Luzon,
quinary, 47.
Nummulina ramondi, 59.
variolaria Brady, 58, 59.
Nummiulites, 61, 73.
elegans, 67.
fichteli, 67.
irregularis Mich., 74.
marginata Mich., 74.
niasi Verbeek, 75.
niasi I Verbeek, 58, 75.
niasi II Verbeek, 58.
subniasi Douvillé, 58.
O
Ocnus imbricatus Semper, 314.
pygmeus Semper, 314.
06, 284.
Oil, fish, 291.
Oligodon iwahigensis Griffin, 260.
modestus Giinther, 260.
notospilus Giinther, 260.
schadenbergii Boettger, 260.
Omens, 83.
Opereculina, 61.
ecomplanata, 76.
costata d’Orb., 56, 57.
costata var. tuberculata Dou-
villé, 56, 76.
Ophites aulicus (Linneus), 258.
subcinctus (Boie), 258.
tesselatus (Jan), 258.
Opisthoglypha, 262.
Orbitoides, 56, 57, 76, 61, 73.
carteri, 60, 61, 62.
dispansa, 59.
gigantea, 60, 62.
insule-natalis Jones et Chap., 71.
martini, 66.
papyracea Brady, 59, 62, 73.
radiata, 61.
340
Orbitoides richthofeni, 66.
sumatrensis, 59.
Orbitolites, 55, 76.
martini? Verbeek, 55.
Oriolus steeri Sharpe, 46.
Ornithology. Notes on the digestive system
of Hydrocorax, 31; notes on a collection
of birds from northern Negros, 39; newly
discovered breeding places of Philippine
sea birds, 167; hybridism among boobies,
179; record of a Puffinus new to Philip-
pine waters and description of a new
species of Micranous, 183.
Orthophragmina, 61, 67.
bartolomei Schlm., 72.
Osmotreron axillaris (Bonaparte), 40.
Osteology. The skeleton in the
lemurs, Galeopteride, 139, 185.
Otolithes argenteus Kuhl: and Van Hasselt,
310.
leuciscus Giinther, 310.
Oxyrhadium leporinum (Giinther), 258.
modestum (Duméril et Bibron),
258.
Ozopemon fuscicollis Hagedorn, 24.
gravidus Blandford, 24.
laevis Strohmeyer, 22, 24.
major Strohmeyer, 23, 24.
obanus Hagedorn, 24.
regius Hagedorn, 24,
rugatus Blandford, 24.
sumatranus Blandford, 24.
theklae Hagedorn, 24.
flying
theklae var. singalangicus Hage-
dorn, 24.
var. sirambeanus Hage-
dorn, 24.
P
Paghing, 88.
Palatak, 213.
Paleontology. Les Foraminiféres dans
Tertiaire des Philippines, 53.
Palipal, 84.
Pango, 92.
Pardaliparus elegans (Lesson), 45.
Pearl buttons, 300.
Pearl-oyster shells, 300.
PEARSE, A. S., On the Habits of Thalas-
sina anomala (Herbst), 218; Concerning
the Development of Frog Tadpoles in Sea
Water, 219.
Penelopides panini (Boddaert), 42.
Petrodromus, 193.
Phapitreron maculipectus Bourns and Wor-
cester, 40.
nigrorum Sharpe, 41.
Philippine fishery resources, 283.
sea birds, newly discovered breed-
ing places of, 167.
sea turtles, 291.
snakes, 253.
tortoise-shell, 291.
Philippinen, Beitrag zur Coleopteren Fauna
: der, 331.
Borkenkafer der, 17.
le
INDEX.
Philippines, les Foraminiféres dans le Ter-
tiaire des, 53.
Piesogaster boettgeri Seoane, 268.
Pili, 88.
| Pitpit, 81, 236.
Pitta erythrogastra Temminck, 43,
Placuma placenta Linn., 296.
PLANTA, FEDERICO S. See BEAN, ROBERT
BENNETT,
Platydactylus abnormis Hichhoff, 25,
sexspinosus Motsch., 25.
Platypus caliculus, 27.
; jansoni Chapuis, 26.
lepidus Chap., 17, 27.
schultzei Strohmeyer, 26.
setaceus Chap., 17.
turbatus Chap., 17.
Polydactylus plebeius (Brouss.), 310.
Polygamy, 132,
Polyodontophis bivittatus Boulenger, 256.
Polystomella, 58, 76.
craticulata, 58.
Polystomella sp., 75.
Potamogale, 193.
Pratincola caprata (Linneus), 45.
Precious coral, 305.
Prioniturus discurus (Vieillot), 41.
Prionochulus sp., 236.
Protaetia banksi Moser, 332.
Proteroglypha, 264.
Psammodynastes pulverulentus (Boie), 264,
Pseudorhabdium longiceps (Cantor), 261.
oxycephalum (Giinther),
262.
Pseudoxenodon dorsalis (Giinther), 268.
Psolus boholensis Semper, 313.
boholensis pandanensis Semper, 313.
complanatus Semper, 313.
Pteropus, 139.
Puffinus chlororhynchus Gould, 183.
Punishments for crimes, 131.
Ptok, 96.
Pupu-lo, 309.
Python reticulatus (Schneider), 255.
| R
Red organ-pipe coral, 307.
| Reef corals, 307.
REVIEWS (BOOK):
Allin, Benjamin Casey: Allin’s Stand-
ard English-Visayan Dictionary, 281.
Bean, Robert Bennett: The Racial
Anatomy of the Philippine Islanders,
| 223. :
Kofoid, Charles Atwood: The Biological
Stations of Europe, 221.
Seidenadel, Carl Wilhelm: The First
Grammar of the Language Spoken by
the Bontoe Igorot with a Vocabulary
and Texts, etc., 271.
The Provinces of China, Together with
a History of the First Year of H. I. M.
Hsuan Tung, and an Account of the
Government of China, 51.
Rhabdornis longirostris McGregor, 45,
mystacalis (Temminck), 45.
INDEX. 341
Rhipidocyclina, 61.
Rhipidura albiventris (Sharpe), 43.
Rotalia, 57, 76.
schroteriana, 57.
Runo, 83, 231.
Rupruppuue, 309.
Rynchocyon, 157.
SS)
Samong, 301.
Sargassum siliquosum J. Ag., 309.
SCHEERER, OTTO, On a Quinary Notation
among the Ilongots of Northern Luzon, 47 ;
review of the Provinces of China, 51;
review of Seidenadel’s The First Grammar
of the Language Spoken by the Bontoc
Igorot, 271. p
Scyllium capense Mull. and Hen., 312.
marmoratum Gray and Hard, 512.
Sea cucumber, 283.
Sea snail, 302.
Sea turtles, Philippine, 291.
SEALE, ALVIN, The Fishery Resources of
the Philippine Islands. Part IV, Miscel-
laneous Marine Products, 283.
Seaweed-isinglass, 309.
Seidenadel, Carl Wilhelm: The First Gram-
mar of the Language Spoken by the Bon-
toe Igorot with a Vocabulary and Texts,
ete., reviewed, 271.
Shark-fin industry, 289.
Shell, conic, 301.
great top, 301.
green snail, 302.
tortoise, 291.
Shorea robusta, 20.
SHUFELDT, R. W., The Skeleton in the
Flying Lemurs, Galeopteride, 139, 185.
Skin, cayman, 310.
crocodile, 310.
shark, 291.
Sky World, 88.
Slavery, 131.
Snakes, check-list and key of, 253,
Solenodon, 193.
Sorex, 161, 193.
Sorites, 56.
Spherotrypes barbatus Hagedorn, 20.
blandfordi Schaufuss, 20.
coimbatorensis Stebbing, 19.
globulus Blandford, 79.
philippinensis Strohmeyer, 18,
20.
pila Blandford, 79.
siwalikensis Stebbing, 29, 20.
tanganus Schaufuss, 20.
Spilornis panayensis Steere, 41.
Stegonotus dumerillii Boulenger, 259.
muelleri Duméril et Bibron, 259.
Stegostoma tigrinum Linn., 372.
Sterna boreotis Bangs, 170.
fuscata Linneus, 171.
gracilis Gould, 168.
melanauchen Temminck, 168.
Stichopus naso Semper, 315.
variegatus Semper, 315.
Stomach in Hydrocorax, lining of, 31.
STROHMEYER, H., Borkenkafer der Phil-
ippinen, 17.
Sula cyanops (Sundev.), 175, 179.
leucogastra, (Boddaert), 168, 179,
piscator (Linneus), 168,
Surniculus velutinus Sharpe, 42.
Susong-dalaga, 301.
Synapta beselii Jeger, 314..
dubia Semper, 314.
glabra Semper, 314.
gracilis Semper, 314.
grisea Semper, 314.
indivisa Semper, 314.
innominata Ludwig, 314.
molesta Semper, 314.
nigra Semper, 314.
pseudo-digitata Semper, 314.
recta Semper, 314,
reticulata Semper, 314.
similis Semper, 314.
T
Tachornis pallidior McGregor, 42.
Tafei, 83.
Talpa europea, 156,
Tanygnathus lucionensis (Linneus), 41.
Taopan, 129,
Tapui, 83.
Taragomi, 133.
Tatik, 310.
Taugh, 84.
Tayaban, 94.
Tentacles, pallial, of Lima species, 327.
Tertiaire des Philippines, Les Foraminiféres
dans le, 53.
Thalassina anomala (Herbst), 213.
Thalassochelys caretta Linn., 292.
Theobroma cacao Linn., 21.
Thread-fin, 310.
Thriponax hargitti Sharpe, 42.
Thyone rigida Semper, 313.
villosa, Semper, 313.
Thyonidium cebuense Semper, 313.
Tigyama, 133.
Tingap, 84.
Toglai and Toglibon, 129.
Toglibon, 129.
Tomicus perforans Wollaston, 24.
Topidonotus aff. hypomelas Giinther, 268.
Tortoise-shell, Philippine, 291.
Trepang, 283.
Trimeresurus flavomaculatus (Gray), 267.
gramineus (Shaw), 267.
halieus Griffin, 268.
schultzei Griffin, 267.
sumatranus (Raffles), 267.
wagleri (Boie), 267.
Trochus, 301.
niloticus Linn., 301.
Tropidonotus dorsalis Giinther, 268.
Tryonyx japonicus Schlegel, 295.
342
Tubipora spp., 307.
Tukab, 233, 239,
Tumtnoh, 237.
Tungob, 238.
Tii-ol, 244.
Tupaia, 193.
Turbo, 302.
Marmoratus Linn., 301, 302,
Turtle, edible, 295.
green, 292,
hawksbill, 291.
loggerhead, 292.
Turtles, Philippine sea, 291.
Typhlogeophis brevis Giinther, 262.
Typhlopide, 254.
Typhlops braminus (Daudin), 254.
cumingii (Gray), 255.
jagori Peters, 254.
olivaceus (Gray), 255.
ruber Boettger, 255,
ruficauda (Gray), 255.
U
Umbrina, 310.
Under World, 88.
Uroloncha evertti
Uyaue, 81.
Vv
Vicarya callosa, 55, 66.
Viperide, 267.
(Tweeddale), 46.
INDEX.
Ww
Window-shell, 296,
Wiwik, 98. :
WORCESTER, DEAN C., Newly Discovered
Breeding Places of Philippine Sea Birds,
167 ; Hybridism among Boobies, 179.
X
Xantholema roseum (Dumont), 42.
| Xeocephus rufus (Gray), 43.
Xyleborus abnormis Hichhoff, 25.
capito Schauf, 77.
kraatzii Eichh., 24.
kraatzii var. philippinensis Hichh.,
17, 20.
perforans Wollaston, 24.
perforans var. philippinensis
Eichh, 25.
Y
Yacal, 719.
Yungipicus maculatus (Scopoli), 42.
Z
| Zaoeys carinatus Ginther, 259.
luzonensis Giinther, 259.
| Zenopeltide, 255.
Zenopeltis unicolor Reinhardt, 255.
Zonophaps poliocephala (Hartlaub), 41.
Zosterops nigrorum Tweeddale, 45.
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