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THE

VOYAGE’ OF’ H.M.8. CHALLENGER.
ZOOLOGY.

REPORT on the Pycnoconipa, dredged by H.M.S. Challenger during the

years 1873-76. By Dr P. P. C. Hoek, Assistant at the Zootomical

Laboratory of Leiden University.

Tue beautiful and rich collection of Pycnocontpa formed during the expedition of

the Challenger has been placed in my hands by Professor Sir Wyville Thomson, F.R.S.,
for description in the official report of the voyage.’

Our knowledge with regard to the Pyenogonids in general, their systematic arrange-
ment, their geographical distribution, &c., is still very insufficient ; and with respect to
those of the greater depths of the ocean hardly anything is known.

The first attempt towards a monograph of the Pycnogonida is that of George
Johnston.” His paper was published in 1837, and treats of the British species known up
to that time. Though no special paper on Pycnogonids seems to have been published.
previous to Johnston’s, yet there are several works of an older date, in which descrip-
‘tions of species and genera belonging to this group occur, as well as discussions as to
their place in the Zoological System. But as the descriptions are for the greater
part very incomplete and the species therefore not to be recognised, these works are
interesting only in so far as they show how much uncertainty has always been felt as to
the place of the Pycnogonids among the Arthropoda.

Linneus (1767) * brings the forms known to him under the genus Phalangium,
in which also numerous land-spiders are placed, and which he ranges between
Hydrachna and Aranea under his Insecta aptera.

* T wish to tender my sincere thanks to Professor Sir Wyville Thomson, F.R.S., &e., who liberally trusted to me—
though a stranger—the drawing up of this report ; at the same time to Mr John Murray who has kindly given me
much valuable assistance.

* George Johnston.—An Attempt to ascertain the British Pycnogonide, in The Magazine of Zoology and Botany,

conducted by W. Jardine, P. J: Selby, and G. Johnston, vol. i., 1837.
> Carolus Linnzus, Systema Nature, editio xii. rev., 1766.

(ZOOL. CHALL, EXP,—PART x.—1881.) ® KI
v3

2 THE VOYAGE OF H.M.S. CHALLENGER.

Otho Fabricius (1780)! assigns to them the name Pycnogonwm proposed by
Briinnich, and places the Cyamus ceti with them in the same genus. He believes them
to be most closely allied to Crustaceans.

J. C. Fabricius (1794)? places the two genera Pyenogonum and Nymphon along with
Pediculus, Acarus, &e., in the eleventh class (the Antliata) of his entomological system.

Lamarck (1801) ® gives the same genera (Pycnogonum and Nymphon) a place in the
class of the Arachnida, order of the Palpistes, together with Bdella, Acarus, and Hydrachna.

Savigny (1816) * proposes to place the Pycnogonida among the Crustacea, an opinion
afterwards embraced by Milne-Edwards (1834)*’ and Johnston (1837). According to
Johnston, Savigny arrived at this conclusion by a very ingenious analysis of their organs.
He pointed out that the proboscis of the Pycnogonum is a head, whereas the mandibles,
palpi, and ovigerous organs are merely modifications of the legs, so that the Pyenogonida,
like the Crustaceans, really have seven pair of legs, &c.

Johnston ° himself, taking the assertions of Savigny as decisive, disagrees with those
naturalists who object to the Pycnogonids being placed among the Crustaceans on
account of the great simplicity of their anatomy. With Milne-Edwards he considers the
Pyenogonids, although imperfect and even degraded, as formed on the same general plan
as that of all the numerous other animals rightly placed in the class Crustacea.

There can be no doubt that Johnston’s publication is one of the most important
in the history of the knowledge of the group. Johnston gives a very clear descrip-
tion of the body of a Pyenogonid, fully discusses the systematic position of the order,
proposes good characteristic marks for the genera, and enters into detailed descrip-
tions of the species. The number of genera in his paper amounts to five (Nymphon,
Pallene, Orithyia, Phoxichilus, Pycnogonum), each with one species, with the exception
of the genus Nymphon, to which two species are assigned.

Of the authors who come after Johnston, Milne-Edwards is the first to be mentioned.
In the third volume of his Histoire naturelle des crustacés (1840), he gives a very short
description of the body of a Pycnogonid, and enumerates, but without paying special
attention to the group, the species and genera known to him. — Following Johnston as
nearly as possible, he has the same five genera‘ and almost the same species. His descrip-
tions are very insufficient ; his work derives importance only from the circumstance that
he places—as I have already mentioned above—the Pycnogonids among the Crustaceans

as a distinct order, viz., that of the Araneiformes.

Othonis Fabricii Fauna Groenlandica, Hafniz et Lipsie, 1780.

* Joh. Christ. Fabricii Entomologia Systematica emendata et aucta, tom. iv., 1794.

3 J. B. Lamarck.—Systime des animaux sans vertebres, 4 Paris, an. ix., 1801.

* J. C. Savigny—Mémoires sur les animaux sans vertébres, premidre partie, 1816.

° H. Milne-Edwards.—Histoire naturelle des Crustacés, tom, i.-iii., 1834-40.

® In this introduction only the most important authors are meuupcele a much fuller list is given by J obnston i in
his An Attempt, &c., and by Milne-Edwards, loc. cit.

7 The name Orith, yia of Johnston “ étant déja employé pour un autre genre de Crustacé,” is changed by Milne iaceneede
into Phoxichilidiumd|.c., p. 535).

I].—Report on the Pycnoconipa dredged by H.M.S. CuaLtencer, during the years
1873-1876.

By Dr P. P. C. Horx, Assistant at the Zootomical Laboratory of Leiden University.

(Received February 20, 1881.)

REPORT ON THE PYCNOGONIDA. 3

The species of the English coast found (1842—44) a new monographer in Goodsir,!
who in three consecutive papers enumerates a large number of species new to the fauna
of the British Isles and to science in general. Two new genera (Pephredo and Pasithoe)
are proposed by him, but owing to the want of detail Mr Goodsir’s papers are of little

value, for it is absolutely impossible to recognise either his new genera or his new species
from such descriptions as he gives.

Of as little value is the list given by base (1864), in which all Goodsir’s species
are found, in addition to some new Ammotheas and species of his new genus Achelia.
Since Hodge’s list—though occasionally in English periodicals short descriptions of new
species. have been published—no special paper on the Pycnogonids of the English coast
has appeared.

Those of the Norwegian coast found a very able describer in Kréyer (1845),’ who
gives very clear diagnoses of the genera and species. As a new genus he proposes
Zetes, and the total number of species described by him is twelve. These descrip-
tions were published without illustrations; but illustrations to the text may be found
in Quoy and Gaimard’s Voyages en Scandinavie, Laponie, &c., Zoologie, Crustacés,
pl. xxxix. (1840).

For the Pyenogonids of Northern Europe and the coasts of the Arctic Ocean, besides
Kréyer, the following authors must be mentioned :—Otho Fabricius‘ for the coast of
Greenland, as mentioned above. Sabine® (1824) describes two Nymphons (N. grossipes and
N. hirsutum) and a species of Phoxichilus (P. proboscideus—a true Colossendeis, Jar-
zyusky), found on the shores of the North Georgian Islands. Bell (1855),° in Belcher’s
Last of the Arctic Voyages, gives descriptions and drawings of two new species of Nym-
phon (N. hirtipes and N. robustwm) common in higher northern latitudes. Jarzynsky (1870)'
enumerates the species of Russian Lapland and the White Sea. A new genus (Colos-
sendeis) is proposed by him. Buchholz (1874),* in the narrative of the second German
North Polar Expedition, enumerates three species of Nymphon, but none of these are new.

1 Harry D. S. Goodsir.—Edinburgh New Philosophical Journal, vol. xxxii., 1842; ibid., vol. xxxiii., 1842; On the
Specific and Generic Characters of the Araneiform Crustacea, Annals and Mag. of Nat. Hist., vol. xiv., 1844.

? George Hodge.—List of the British Pycnogonoidea, with descriptions of several new species, Ann. and Mag. of
Nat. Hist., vol. xiii., 3d series, 1864.

3 Henrik Kroyer.—Bidrag til Kundskab om Pyknogoniderne eller Sospindlerne, Natur-historisk Tidskrift, Ny
Raekke, i., 1845,

4 Loe. cit. ;

5 A Supplement to the Appendix of Captain Parry’s Voyage for the Discovery of a North-West Passage in the
years 1819-20, containing the Zoological and Botanical Notices, London, 1824; Marine Invertebrate Animals, by
Captain Edward Sabine.

6 Thomas Bell—Account of the Crustacea of the Last of the Arctic Voyages in Search of Sir John Franklin,
under the command of Captain Sir E. Belcher, C.B., &c., in two volumes, vol. ii., 1855.

7 Th. Jarzynsky.—Promissus catalogus Pyenogonidarum inventarum in mari glaciali ad oras Lapponie rossice et
in Mari albo, anno 1869 et 1870, Annales de la Soe. des Natur. de St Petersb., 1870.

8 R. Buchholz.—Crustaceen der Zweiten Deutschen Nordpolarfahrt, Anhang; Pycnogonida, Die Zweit Deutsche
Nordpolarfahrt, ii. 396, 1874.

+ THE VOYAGE OF H.M.S. CHALLENGER.

Heller (1875) ? proposes two new species of the same genus gathered during the Austrian
North Polar Expedition ; both are identical with species described before under other

names.

In 1877 and again in 1879 G. O. Sars* published lists of the Pyenogonids gathered
during dredging cruises in the northern part of the North Atlantic, on the coast
of Norway, &. There are in all four new species of Nymphon (N. megalops,
N. macronyx, N. serratum and N. pallenoides), a new genus, Ascorhynchus, with the
species Ascorhynchus abyssi, a new species of Colnseqimiss (C. angusta), and a. new
Pallene, P. malleolata.

Miers (1877)°* treats of the Pycnogonids collected during the last English Arctic
Expedition. He gives two species, neither of which is new, and describes a variety of
Nymphon hirtum.

In regard to the coast of Germany and the Netherlands not a single species has been
recorded which is not found on the English coast. Occasionally enumerations of species
have been published by Frey and Leuckart,* and Bohm.’ In a paper I published myself
(1877) ° I described the four genera, species of which are found on the Dutch coast.

The Pycnogonids of the French coast have been studied by Quatrefages (1844),’
Claparéde (1863),° Hesse (1867-74),’ and Grube (1868-72).” Their studies resulted in
the proposal of a new species of Ammothea (A. pycnogonoides, Quatr.), of a new
Phoxichilidivin (2) (P. cheliferum, Claparéde), a new species of Phowichilus (P. levis,
Grube), and two new genera (?) Oiceobathes, Hesse, and (?) Oomerus, Hesse, both very
insufficiently described. The Pycnogonids found on the coasts of France, the British
Isles, Germany, &c., are not yet sufficiently well known to allow of their geographical
distribution being discussed.

About the species of the Mediterranean very little is known. Philippi (1843) " and

1 Camil Heller.—Die Crustaceen, Pycnogoniden, und Tunicaten der K. K. Oester. Ungar. Nordpol. Expedition,
Denkschriften der Mathematisch-Naturwiss. Classe der K. Akad. der Wissensch., Bd. xxxy., Wien, 1875.

2 G. O. Sars.—Prodromus descriptionis Crustaceorum et Pycnogonidarum, quae in expeditione Norvegica, anno 1876,
observavit, Arch. f. Math. og Naturvid., ii., 1877 ; Crustacea et Pyenogonida nova, quae in itinere 2 et 3tio expeditionis
Norvegice, anno 1877 et 1878, collecta (Prodromus descriptionis), ibid., iv., 1879.

3 Edward J. Miers.—Report on the Crustacea collected by the Netairaliats of the Arctic Expedition in 1875-76
Annals and Mag. of Nat. Hist., fourth series, vol. xx., 1877.

4 Frey und Leuckart. —Beitrige sur Kenntniss qaxbellgser Thiere, 1847.

5 R. Bohm.—Ueber die Pyonvgoniden des Konig]. Zool. Museums zu Berlin, Monatsber. der Konigl., Akad. der Wiss.
1879.

5 Pp. P. C. Hoek.—Ueber Pyenogoniden, Niederl. Archiv. f. Zoologie, iii., 1877.

7 A. de Quatrefages.—Mémoire sur Vorganisation des Pyenogonides, Ann. d. Sc. Natur., 3™¢ Série, Zoologie, tom.
iv., 1845.

8 A. René Edouard Claparéde.—Beobachtungen tiber Anatomie und Entwickelungsgeschichte wirbelloser Thiere
an der Kiiste von Normandie angestellt, 1863.

® Hesse.—Annales des Sciences naturelles, 5!™¢ Série, vii., 1867 ; ibid. 5!me Série, xx., 1874.

© Edward Grube.—Mittheilungen iiber St Malo und Roscoff und die dortige Meeres besonders die Anneliden-fauna
1869 ; Mittheilungen tiber St Vaast la Hougue, und seine Meeres, besonders seine Anneliden-fauna, Verhandl. der
Schlesischen Gesellsch. f. vaterl. Cultur., 1869.
1 A, Phillipii—Ueber die Wenpalitaniscte n Pyenogoniden, Arch, f. Naturgesch, ix., 1843.

REPORT ON THE PYCNOGONIDA. 5

Costa (1838—61)* published short notes on the Pycnogonids found there. Philippi proposed
a new genus(Hndeis), which is perhaps identical with Pasithoe, Goodsir; and a second genus
(Pariboea), with the species Pariboea spinipalpis. Costa introduces (1838) the genus
Phanodemus, in all probability identical with Pephredo, Goodsir; in his Microdoride medi-
terranea (1861) he proposes three new genera: Rhynchothorax, Platychelus, and Aleynous.
From the Gulf of Naples Costa knows in all seven species, whereas the total number of
species of the Mediterranean found in Philippi’s paper is only four. A monograph on
_ the Pycnogonids of the Mediterranean, and especially of the Gulf of Naples, will very pro-

bably soon appear ; it will form the second part of the Studi e Ricerche di Cavanna (1877),”

and will also be published by Dohrn, as announced in his Neue Untersuchungen (1878).”

Of all Pycnogonida, those found on the west coast of North America are best known.
Careful attention was paid to them by Stimpson (1852),* Verrill, Smith (1874),’ but
especially by Wilson (1878-80),° who in his Pyenogonida of New England, enumerates
fourteen species belonging to nine genera, two of which (Psewdopallene and Anoplo-
dactylus) are new to science. Though I do not believe that these new genera after a
careful examination will hold good, and though I think it a pity that Wilson in his
researches has not taken advantage of recent investigations (especially those of Cavanna),
yet there can be no doubt, I believe, that his paper is one of the best descriptive publi-
cations after those of Johnston and Kroyer.

For the other countries of our globe, a very brief enumeration may suffice. As far
as I have been able to ascertain, by far the greater number of the species described are
littoral ; from the open ocean very few species are recorded. ‘Two species described by
White (1847),’ inhabiting the South Sea, are exceptions. White describes them as species

‘of Nymphon, whereas I believe that they ought to be considered as Phoxichilidiums.
From the open ocean are also those species (one of Mymphon, another of Phowichilidium)
mentioned by Grube (1869)* as occurring in the China Sea. Grube’s descriptions as
well as those of White are extremely incomplete.

Wood-Mason (1873)° described a species of a genus which he believed to be new,

1 QO. G. Costa.—Fauna del Regno di Napoli, Crostacei et Aracnedi, Napoli, 1838 ; Microdoride mediterranea, tomo
primo, Napoli, 1861.

2 G. Cavanna.—Studi e Ricerche sui Picnogonidi, parte prima (Publicazioni del R. Istituto di Studi superiori
pratici et di perfezionamento in Firenze, Sezione di Scienze fisiche e naturali), Firenze, 1877.

3 A. Dohrn.—Neue Untersuchungen iiber Pyenogoniden, Mittheil. a. d. Zoologischen Station zu Neapel, i., 1879.

# William Stimpson.—Synopsis of the Marine Invertebrata of Grand Manan, Smithsonian Contributions to Know-
ledge, January 1853.

5 Smith in Report on the Invertebrata of Vineyard Sound. In Part I. of the Report on the Condition of the Sea-
Fisheries of the South Coast of New England, 1873.

6 E. B. Wilson.—Descriptions of Two New Genera of Pycnogonida, American Journal of Science and Arts,
vol. xv., 1878 ; Synopsis of the Pycnogonida of New England, Transactions of the Connecticut Academy, vol. v., 1880.

7 Adam White——Descriptions of New or Little-Known Crustacea in the Collection at the British Museum, Pro-
ceedings of the Zoological Society of London, part 15, 1847.

8 E. Grube in Jahresbericht der Schlesischen Ges. fiir vaterlandische Cultur, Breslau, 1869.

® James Wood-Mason.—On Rhopalorhynchus kréyert, a new Genus and Species of Pycnogonida, with plate xiii.,
Journal of the Asiatic Society of Bengal, part 2, 1873.

6 THE VOYAGE OF H.M.S. CHALLENGER.

and called Rhopalorhynchus: There can be no doubt that this is the same as the
genus formerly (1870) described ‘by Jarzynsky * as Colossendeis. Wood-Mason’s species
is an inhabitant of Port Blair, Andaman Islands.

Miers (1875 and 1879) ° mentions two species of Nymphon, and one of a new genus,
which he calls Tanystylum, and which is nearly allied to Achelia. These species were
collected at Kerguelen Island during the visit of the English and American Transit of
Venus expeditions to that Island. Béhm (1879)° has made a very careful study of the
Pyenogonids of the Royal Zoological Museum at Berlin. He describes two species of
Nymphon and one of Achelia, as collected at Kerguelen; one species of Nymphon col-
lected south of the Cape of Good Hope, one Pallene (?) taken in the Straits of Magellan,
another Pallene from Mozambique, a Phowichilidium and a Phoxichilus collected in
the neighbourhood of Singapore ; finally, besides some species from Northern Europe,
three species found near Enosima (Japan); one species of a new genus, which Bohm
calls Lecithorhynchus, one Ascorhynchus (Gnamptorhynchus, Bohm), and one species of
Pallene. Slater (1879)* published a short paper on a new genus of Pyenogonids (Para-
zetes) found in Japan, and described in the same paper a variety of Pycnogonwm litorale
from the same country.

In the Boston Journal of Natural History, Eights (1836 ?) mentions the genus Decalo-
poda, but I have not been able to ascertain whether this is a good genus, nor where it
has been found.’ <A species of Pasithoe described by Dr Gould’ is, according to Wilson
(loc.cit. p. 2), “indeterminable.” To Mr Wilson’s paper I am also indebted for the men-
tion of a species of Pycnogonid found on the coast of Chili: it seems to be a species
of Pycnogonum.’

In this enumeration the reader will not find a complete list of the descriptive litera-
ture of Pyenogonida, but all the more important publications, together with the greater
number of the minor papers on our group are mentioned. With a few exceptions the
zoological publications about Pyenogonids are very superficial, and this I believe is owing
partly to the circumstance that many authors who have had no opportunity of comparing
large collections of different forms have published descriptions of species and even of
genera from the examination of such species only. To describe new species, however, ought

1 Th. Jarzynsky, loc. cit.

2 E. J. Miers.—Descriptions of new species of Crustacea collected at Kerguelen’s Island, by the Rev. A. E. Eaton.
Annals and Magazine of Natural History, fourth series, vol. xvi., 1875 ; Crustacea of Kerguelen Island, Philosophical
Transactions, London, vol. elxviii. ; extra volume, pp. 200-214, 1879, pl. xi.

5 R. Bohm, loc. cit.; the same in Sitzungsberichte der Gesellschaft naturforschender Freunde in Berlin, 1879,
pp. 53 and 140,

* Henry H. Slater.—On a new genus of Pyenogon (Parazetes) and a variety of Pycnogonwm littorale from Japan
Ann. and Magaz. of Nat. History, 5th series, vol. iii., 1879.

® Boston Journal of Natural History, i. 204, t.7. (See Cuvier’s Animal Kingdom, London, Wm. S. Orr & Co.,
1840, p. 468.)

® Proc. Boston Society Nat. Hist., vol. i. p. 92.
7 Gay.—Historia fisica y politica de Chile, Zoologia, p. 308, pl. iv. fig. 8, 1854.

REPORT ON THE PYCNOGONIDA. t

not to be the work of one who begins to study a group, as is often the case, but can
only be done properly after laborious and continuous research. Moreover, the study of
the literature is enormously encumbered by the circumstance, that descriptions of single
species often lie buried in obscure periodicals. This circumstance, I hope, will be
considered, when my report is found to be far from complete.

The collection of Pyenogonida brought home by the Challenger and need in my
hands numbers about 120 specimens. They were in an excellent state of preservation,
and to facilitate the work, the bottles of spirit in which they were put, were furnished
with labels indicating the station, latitude, longitude, bottom temperature, and the
nature of the’ sea-bed where they were dredged. Some of the specimens were not
obtained from any of the 361 dredging stations, but were collected on the shore (near Cape
Town, e.g.), or dredged in shallow water (Bahia, Kerguelen). Over a course of 68,890
miles the dredge was let down at 361 stations, and Pycnogonids were procured on only
twenty-six occasions. The 120 specimens of Pyenogonida brought home belong to
thirty-six species, and thirty-three of these I have been obliged to consider and describe
as new to science. The greatest depth where a Pycnogonid was found was 2650 fathoms ;
the greatest depth dredged during the cruise was 4575 fathoms.

- In the following list I have given the range in depth at which species of Pycnogonida
were found by the Challenger, and also recently during the cruise of the “ Knight
Errant” :—

Shore, . : : A Discoarachne brevipes, Hoek.
re : c 6 Hannonia typica, Hoek. '
7 to 20 asee : : Phoxichilidium fluminense, Kroyer.
“6 3 y : 5 Phoxichilidium insigne, Hoek.
10%0:120 _,, : : Nymphon brachyrhynchus, Hoek.
25 +0120 ,, - : Nymphon brevicaudatum, Miers.
25 4 : c Nymphon fuseum, Hoek.
38 oF é : Ascorhynchus minutus, Hoek,
op 5 ; Fi Pallene languida, Hoek.
38 to 40 ,, ; 3 Pallene laevis, Hoek.
38 to 120 _ =r, . . Pallene australiensis, Hoek.
45, 55,175 ,, : ; Phoxichilidium patagonicum, Hoek.
53 5 5 3 Pycnogonum litorale, Strom.
55, 70, 120 ,, . : Colossendeis megalonyx, Hoek.
83 ¢ 7 9 : Nymphon brevicollum, Hoek.
83 to 540 _—s—*,, ; és Nymphon grossipes, Oth. Fabr., sp.
120 “ x 5 : Colossendeis robusta, Hoek.
150 : op : ; Ascorhynchus orthorhynchus, Hoek.
375 to 540, 0 . Nymphon robustum, Bell,
400 to 1600 _,, . ; Colossendeis leptorhynchus, Hoek.
515, 530, 540 ,, ‘ . Nymphon strémii, Kroyer.
540 : x ; 0 Nymphon macronyx, G. O. Sars.
+ “ ; Colossendeis proboscidea, Sab., sp.

600 . op . ; Phoxichilidium patagonicum, var. elegans, Hoek.

8 THE VOYAGE OF H.M.S. CHALLENGER.

700 fathoms, A . Oorhynchus aucklandie, Hoek.

825 : as é : Nymphon perlucidum, Hoek.
1100 ° op : 4 Nymphon longicoxa, Hoek.

‘ : A} : A Nymphon compactum, Hoek.
1250 5 x , : Colossendeis minuta, Hoek.
1375 : n : 5 Ascorhynchus glaber, Hoek.
1375 to 1600 _,, : 5 Nymphon hamatum, Hoek.

iS . of - ‘ Colossendeis gigas, Hoek.

- 35 5 ; Colossendeis gracilis, Hoek.
1600 to 1950 _,, “ ‘ Phowichilidium pilosum, Hoek.
1675 5 " - : Nymphon meridionale, Hoek.

+ 4 a 2 : Phowxichilidium oscitans, Hoek.
1875 F o) : : Phoxichilidium mollissimum, Hoek.
2160 - 5 : ; Nymphon procerum, Hoek.
2225 IS ; 3 Nymphon longicollum, Hoek.

ee : =F : 5 Collossendeis media, Hoek.
2650 : $ a : Colossendeis brevipes, Hoek.

The number of times at which Pycnogonida were dredged at certain depths is shown
in the following table :—

99 dredgings in depths of from lto 500 fathoms, . : 26 times. Y

30 5 3 501 to 1000 so, : : a) >

47 7 5 1001 to 1500 =, 2 Ee 3} op

47 x, op 1501 to 2000 _—S—,, : : A 55

93 5 x 2001 to 2500 _—ti, 3 : Ph

83 ” ” 2501 to 3000 =» - . Once (at 2650 fathoms).
11 = Ay 3001 to 4575 35 ; ; None. :

It thus becomes apparent that what Davidson has shown for the Brachiopoda,
holds also in the case of the Pycnogonida, that they are very seldom found in depths
exceeding 500 fathoms ; out of about 100-dredgings in depths of from 1 to 500 fathoms,
Pycnogonids were brought up twenty-six times, while in depths varying from 501 to
3000, they were obtained only thirteen times out of 300 dredgings.

The following statement shows the range in depth at which the genera of Pyenogonida
hitherto known have been found. The total number is twenty-seven genera, of which
eleven are true littoral forms. Of the sixteen remaining genera there are five
of which I am quite uncertain as to the depth at which they are found, and
four for which the depth does not exceed 50 fathoms. Then there are two (Pallene
and Pycnogonum), which, as a rule, inhahit depths not exceeding 120 fathoms, but
which in a single case were found at depths almost reaching 500 fathoms (Pallene
malleolata, G. O. Sars, at a depth varying between 191 and 459 fathoms, and Pyeno-
gonum litorale, dredged by Smith and Harger, at a depth of 430 fathoms). Hence
there remain only five genera of Pycnogonida, species of which may truly be called

deep-sea inhabitants; they are the genera Nymphon, Ascorhynchus, Oorhynchus, Colos-
sendeis, and Phowichilidium.

REPORT ON THE PYCNOGONIDA.

List oF THE GENERA OF PYCNOGONIDA HITHERTO KNOWN.

Name of the Genus.

Nymphon, Fabr.,
Ammothea, Leach,

‘| Bohmia, Hoek, .
Phanodemus, Costa,
Rhynchothorax, Cos., .
Pephredo, Goodsir,
Platychelus, Cos.,
Oiceobathes, Hesse, :
Ascorhynchus, G. O. Sars, .

Zetes, Kroyer,
Parazetes, Slater,
Pariboea, Philippi,
Achelia, Hodze, .

Alcinous, Cos., .
Tanystylum, Miers,
Lecithorhynchus, Bohm,
Oorhynchus, Hoek,
Colossendeis, Jarzynsky,
Pasithoe, Goodsix,
Endeis, Philippi,
Discoarachne, Hoek, .
Pallene, Johnston,

Phoxichilidium, M.-Kdwards,

Oomerus, Hesse, .
Hannonia, Hoek, ° :
Phoxichilus, Laty.,

Pycnogonum, Briinnich,

Number
of Depth in Fathoms

Species | at which they have Geographical Distribution.
De- been found.

scribed,

38 Shore to 2225. | Mundane—Pacific Ocean excepted.

5 Shore to 5. American and European Coasts of the North
Atlantic.

1 (2) (?)

3 Shore. Coast of Italy.

1 Q North Coast of Africa,

1 Shore. Coast of England.

1 (2) Coast of Sardinia.

1 Shore. Coast of France.

D 38 to 1539 North Atlantic, Indian Ocean, South Coast of
Australia, North of New Guinea, Coast of
Japan.

1 Shore. Coast of Greenland,

1 (2) Japan.

1 Shore. Coast of Italy.

4 Shore to 35. American and European Coasts of the North
Atlantic, Coasts of the Mediterranean, Ker-
guelen,

2 (2) Coast of Italy.

2 5 to 7 Kerguelen, East Coast of North America.

2 3 to 4 Japan.

1 700 Auckland.

12 55 to 2650 Mundane—Pacific Ocean excepted.

1 Shore. Coast of England.

2 Shore. Coast of Italy.

i Shore. Coast of Cape Colony.

16 Shore to 459.* | Coast of Northern Europe, Greenland Sea,
Coast of Greenland, East Coast of North
America, Coast of Mozambique, off Australia, |
China Sea, Coast of Japan.

15 Shore to 1950. Coast of Northern Europe, Greenland, North |
America, North Atlantic, Coast of Brazil,
Patagonia, South Atlantic, Indian Ocean,
Coast of Lower Siam, off Japan.

1 Shore. Coast of France.

1 Shore. Coast of Cape Colony,

4 Shore. Coasts of Northern Europe, Mediterranean Coast,
Coast of Lower Siam.

2 Shore to 480,? Coasts of Northern Europe, East Coast of North

America, Coast of Chili, Coast of the Mediter-
ranean, Coast of Australia,

1 Teste G. O. Sars.

(ZOOL. CHALL, EXP,—PART x,—1881.)

2 Smith and Harger, teste Wilson.

K 2

10 THE VOYAGE OF H.M.S. CHALLENGER.

When comparing the bathymetrical range of the different genera with their
geographical distribution, it is easily remarked that it is the genera most widely
spread over the bottom of the sea which are capable of existing at the greatest
variety of depth. This is, for instance, the case with Nymphon, Colossendeis, and
Phowichilidium. Some species of Nymphon are found at low-water mark, others
inhabiting shallow water in the immediate neighbourhood of the coast are dredged at
a depth of under 100 fathoms ; others again are never found at a depth exceeding 800
fathoms, and finally, there are some which are true deep-sea species. Some species of
Colossendeis were dredged at a depth of under 100 fathoms, other species inhabit the
ocean at a depth not exceeding 800 fathoms and others were dredged at depths varying
from 800 to 2800 fathoms. The genus Phowxichilidiwm shows almost the same bathy-
metrical range as Nymphon. Now the geographical range of these three genera is, as
far as I could ascertain from the facts at my disposal, nearly the same ; this distribution
is mundane. With the exception of the Pacific Ocean, from which as yet not a single
species of Pyenogonid has been obtained, representatives of these three genera are found
almost in every sea.

Of the genus Ascorhynchus only five species are known as yet. They were collected
at depths varying from 38 to 1539 fathoms, and at widely distant places, viz., in the
Greenland Sea, between the Cape of Good Hope and Kerguelen Islands, off Australia, to
the north of New Guinea, and off Japan; and as the different species of this genus form
a very natural group, it is, I think, very probable, that later investigations will show also
for interjacent places the occurrence of forms belonging to this same group. Oorhynchus
is as yet the only genus which seems to inhabit depths exceeding 800 fathoms exclusively ;
but as only a single specimen of the one species known of this genus has been collected, I
do not think it expedient to pay much attention to this fact.

Hence, with regard to the bathymetrical range, a close study of the material brought
home by the Challenger, added to what was previously known on the subject, has
shown :—

(1) That those genera which range most widely geographically are also those which
range most widely in depth; and (2), that there does not seem to exist a single true
deep-sea genus of Pycnogonids.*

As for the influence of the increasing depth on the form and the structure of our
animals, this is by no means easily traced. As far as the structure of the integu-
ment and of the eyes is concerned, I will treat the question at some length when speak-
ing of their structure. As a rule the true deep-sea species are more slender, the legs very
long and brittle, and the surface of the body smooth, whereas the true shore-inhabitants
are much more concentrated, have shorter legs, and are often densely covered with

1 From the study of deep-sea forms in general, Mr Moseley and others came to the conclusion that these animals
have a world-wide range. Of this the Pycnogonids give a fair instance, I believe (Moseley in Nature, April 8, 1880,
p. 546).

REPORT ON THE PYCNOGONIDA. 11

hair. However, these rules admit of a great many exceptions. Thus the most common
shallow-water species of the English, French, and Dutch coasts is Nymphon gracile,
Leach, an exceedingly slender animal with very long legs, and moreover almost smooth.
Colossendeis proboscidea, Sab., sp., is a blind species occurring only at a considerable
depth ; yet it has a highly concentrated body with short legs. Two species of Phoai-
chilidium, for which I have proposed the names Phoxichilidium pilosum and Phowichili-
dium mollissimum, are true inhabitants of the depths of the ocean; yet they are not
smooth at all, but covered by avery hairy integument. The case of Phoxichilidium pata-
gonicum and its variety elegans, which I describe hereafter, must probably be considered
as a trifling instance of the effect of depth on the slenderness of the body.

The scientific and trustworthy material at our disposal is by no means suflicient
to enable us to discuss thoroughly the question of the geographical distribution of
Pyenogonids. Judging from what is known of the European and North American
coasts, it is most probable that on all coasts, and everywhere in shallow water in the
neighbourhood of the shore, forms of Pycnogonids will be found occurring ; and as I
think it improbable that any true shore-inhabitant will be found which shows a very
wide range, it is also highly probable that the number of rittoral forms at present known
is very small in comparison with the number really existing.

The distribution of those Pycnogonids which are not to be considered as shore-
inhabitants, but which have never been dredged yet at depths exceeding 500 fathoms,
is best known in the northern part of the Atlantic and the seas corresponding with it
(North Sea, Greenland Sea, Barents Sea). The species of the genus Nymphon, which
occur in the neighhourhood of the coast of New England, are found to the north and
east as far as Greenland, Spitzbergen, and Novaja Semlja; but these Arctic Seas are,
moreover, inhabited by some forms of the same genus occurring there only. As this
point has been more fully discussed by me in another paper, it will suffice merely to
mention it here.

Among the Pycnogonids of the Challenger Expedition, Colossendeis megalonyx,
Hoek, is the only species, which, though found at a depth of from 55 to 120 fathoms, has
a wide range; about the 58th south parallel it was dredged off Kerguelen Island, and
also between Patagonia and the Falkland Isles.

With respect to the true deep-sea species the material is by no means sufticient for
the study of their geographical range. Of the thirty-six species of Pycnogonids brought
home by the Challenger, nineteen are true deep-sea species. Of these only three belong
to the northern hemisphere, viz., Colossendeis minuta, Hoek, south of Halifax ; Phowichi-
lidium oscitans, Hoek, west of the Azores; and Phowchilidium mollissimum, Hoek, off
Yeddo; they were only dredged once and were new to science. Of the remaining sixteen,
which belong to the southern hemisphere, one was dredged at lat. 65° 42’ §.
(Nymphon meridionale, Hoek) and one almost under the equator (Nymphon per-

12 THE VOYAGE OF H.M.S. CHALLENGER.

lucidum, Hoek, at lat. 0° 48’ S.). The fourteen remaining species were all dredged
between lat. 33° 31’ S., and lat. 53° 55’ S.; and it is a remarkable fact, that those
two latitudes limit a zone of about 20°, in which Pycnogonids seem to be rather
common. However, even in this zone they are again much localised, being almost
in every instance from near the coast of an island or continent. For miles the dredge
was let down without bringing up a single specimen; whereas six species were found
occurring at Stations 146 and 147, off the Crozets Islands (these Stations being very
near to one another, I take as one); one at Station 157; three east of New Zealand,
at Stations 168 and 169; five between Juan Fernandez and Valparaiso (Stations 298,
299, and 300); and two east of Buenos Ayres (Stations 320 and 325). |

These facts indicate, I think, that the number of places inhabited by deep-sea
Pyenogonids are not very numerous, and that where Pycnogonids do occur,
many forms are, as a rule, found living together. This also ought to be observed
when considering that between Stations 237 (off Yeddo) and 298 (between Juan
Fernandez and Valparaiso), throughout a course of 11,775 miles, the dredge was let down
sixty times and not a single Pycnogonid was obtained. This of course may partly be
ascribed to the circumstance, that on an average the depth of that part of the ocean is
too considerable to be inhabited by Pycnogonids; but as the depth at many stations
during that part of the voyage did not exceed the depths of other stations at which
Pycnogonids were dredged, this cannot be considered as the only reason. Also when the
same circumstance is found to be the case in that large part of the South Atlantic between
the Azores and Station 146, where during a course of more than 9000 miles the dredge
was let down at 76 stations without a single return of Pycnogonids, and this although
the depth at these stations is less, and at most of them much less, than some of the
greater depths at which Pycnogonids were found, it is quite evident that the depth of
the sea alone cannot be held responsible for it. Nor do I consider it yet proved that
Pycnogonids are totally wanting in these oceans, as only a very small area of these oceanic
abysses has been explored; so I think the only conclusion which at present may be
drawn is this, that as yet only a few of the places where Pycnogonids occur in great
numbers have been found out.

In regard to the nature of the bottom from which the Pyenogonids of the Challenger
Expedition were obtained, conclusions must be also somewhat uncertain. The bottoms
on which they occur seem to be extremely different. We find that one species
was brought up from a bottom of gravel and stones, one from hard ground, one from
rocky ground, five species are recorded as having been brought up from a muddy bottom,
one from diatom ooze, five from a sandy bottom, three from a bottom of grey ooze, three
from grey mud, and three from globigerina ooze. The other species were obtained from
rocky bottoms in the neighbourhood of the shore.

More particulars about the geographical and bathymetrical distribution of the

REPORT ON THE PYCNOGONIDA. 13

Pycnogonids may be found in the list of the species hitherto described, which I append
to this report. I have tried to make it as complete as possible; yet it contains many
species of which no information is given as to the depth at which they were found ; others
of which even the locality they inhabit is not accurately stated; and furthermore, there
are genera and species—and of the latter no small number—about which we are totally
left in the dark. To explain this the reader must keep in mind (1) that this is the first

Immovable claw

WASTAN) cee ac an ar ? A a ae ig aa aan nnn nwenennmrms 3rd coxal joint of the leg
f Palpus

POoBO8CI8 — <a-nennesnveen 0 ee
Ist joint of
the mandible #¥

Cephalic part of the cephalothoracic segment ) 4
eT Skea ene yf / 2nd tibial joint

t
2nd coxal joint
3rd

Thoracic part of th
cephalothoraci:

Ist tarsal joint --------------
2nd thoracic segment

3rd thoracic segment I}

2nd tarsal joint.---
4th thoracic segment

Abdomen ...--. = (fe ee

aM TSN / < ceeeneeaeen Anus

OvigerOUs Veg ma----o-----------enenn---fof
2 Claw

RA ___... Ist tibial joint

ola 2nd tibial joint

Nymphon, sp. *
attempt to make such a list, with the exception of a very incomplete and superficial
enumeration published in 1874 by Semper,’ and (2) that there is as yet no paper
published which discusses the relative value of distinguishing marks, So it is evident
that the making of this list has been an exceedingly troublesome affair, and that some

allowance may be made for its incompleteness.
1 For reasons easily to be understood I have taken a species of Nymphon as the type.

2 ©, Semper, Ueber Pyenogoniden und ihre in Hydroid-Polypen schmarotzenden Jugendformen., Arbeiten des Zool.
Zoot. Instituts in Wirzburg, Band i., 1874,

14 THE VOYAGE OF H.M.S. CHALLENGER,

Before inserting this list I wish to give a short description of the body of a
Pyenogonid, and at the same time to state the nomenclature I have made use of.

The body of every Pycnogonid consists of four segments, the first of which is to be
considered as formed by the connection of the head with the first thoracic segment. At
the anterior end this first segment is furnished with a long and stout proboscis. This
proboscis is situated either about the front of the first segment, as in Mymphon,
and in this case is capable of very limited motion, or as in Ammothea and Ascorhynchus,
though also situated about the front, it is connected with the segment by means of an
articulation, and for that reason is highly movable, or it is, as in Phowichilidiwm,
situated on the ventral surface of the first segment, and bent forward ; or finally, it is
situated about the ventral side, and at the same time lapped over it (Béhmia, mihi).
The form and size of this proboscis varies greatly. . At its extremity it is furnished with
a triangular mouth. It is to be considered as an unpaired outgrowth of the region
surrounding the mouth, and has nothing to do with a true head, as was supposed by
Savigny. Neither is there anatomically or embryologically any real ground for the
opinion, suggested by Huxley,’ that the proboscis represents the united chelicers
and pedipalpi like that of Acarina.?

The cephalic part of the cephalothoracic segment is generally furnished with three
pair of appendages, which long ago received the names of mandibles, palpi, and
ovigerous legs. As far as has been ascertained till now, there is not a smgle genus of
Pycnogonid, which does not show these three pair of appendages either in the adult
state, or during its embryological development. Yet cases are not rare, in which in
the adult animal, either the first (the mandibles) or the second pair (the palpi) or both
are deficient. With respect to the third pair of appendages (the so-called ovigerous legs),
on the contrary, they are never found wanting, as far as we know, in the adult animal
of either sex. Whoever studies different forms of Pycnogonids, will soon discover what
a difference may be caused in the appearance of the cephalic part of the body by the
presence or absence of the cephalic appendages; hence it is that the various authors
who have proposed a classification of the group have largely made use of this presence
or absence of cephalic appendages. Although there is no doubt, I believe, that good
characteristics may be derived from the number of these appendages, the following may
show how extremely necessary it is to be cautious in this matter.

' Huxley, Anatomy of Invertebrated Animals, p. 386, London, 1877.

? On a transverse section, the proboscis of the Peynogonids always shows a more or less distinctly triangular
shape, the mouth is also triangular, &e. The total form, therefore, is to be compared with the fruit of a monocotyle-
donous plant, composed of three carpels. Of these one is placed dorsally, the two others meet longitudinally in the
middle of the ventral side. If anybody should feel inclined to try again to homologise the proboscis with cephalic ap-
pendages, he will have to eall the dorsal piece the labrum, and the two others the homologues of mandibles. However, in
the earliest stages of development I have observed, the proboscis has already the form of a short cylindrical appendage,

and I must point out the anatomical fact that the proboscis for the greater part is innervated from the supraceso-
phageal ganglion.

REPORT ON THE PYCNOGONIDA. 15

The mandibles in some genera are two-jointed (Nymphon, Pallene, &c.), in others
three-jointed (Phoxichilidium). As a rule the second or third joint terminates in
a pair of pincers, with a movable and an immovable claw. Now there are genera, some
species of which show the mandibles small, yet furnished with true pincers, whereas
other species of the same genus show the mandibles in a much more rudimentary state,
as if, for instance, represented only by a single joint terminating abruptly (Ascorhynchus
glaber, Hoek, and A. minutus, Hoek). In other genera the mandibles are in the adult
animal always rudimentary, represented only by short stumps (Lecithorhynchus, Bohm,
Oorhynchus, Hoek, &c.); whereas in a fourth category the mandibles have totally
disappeared (Colossendeis, Phowichilus, Pycnogonum, &c.). Among the specimens of a
species of one of these genera (Colossendeis gracilis, Hoek), dredged during the cruise of
H.M.S. Challenger, I have, however, found one specimen furnished with a pair of
distinctly three-jointed mandibles, terminating in a pair of pincers; and this specimen
was the largest of the three obtained.

The palpi when present show very different numbers of joints. Thus there are only
three in Pephredo, five in Nymphon and Discoarachne, eight in Achelia, nine in
Ammothea and Corniger, ten in Ascorhynchus, Colossendeis, &c. The palpi have
disappeared in the genera Pallene, Phowichilidium, Phoxichilus, Pycnogonum, &e.
In Phowichilidium they are as a rule still represented by rounded lateral processes
placed at both sides of the front part of the cephalothorax, whereas Béhm has observed
a specimen of Pallene furnished with rudimentary, yet distinct two-jointed palpi.

The third pair of appendages, viz., the ovigerous legs, are never wanting in any
species of Pycnogonids. Among the Pycnogonids of the Challenger, there is not even
a single specimen without ovigerous legs! As a rule they are ten-jointed; the first three
joints are extremely small, the two following are the longest of all, the sixth jomt is a
great deal shorter, the last four joints are much shorter still, the tenth joint as a rule
is furnished with a claw. In some genera (Collossendeis, e.g.) the fifth joint is small,
the sixth as long as the fourth jomt. In those genera, where a certain tendency is
observed to drop their cephalic appendages, the ovigerous legs share this fate only to a
small extent. As the functions of the ovigerous legs are twofold, one being to bear the
egos, a function only accomplished by the male,’ the other to serve as an organ of feeling,
also, in all probability, of seizing the food, and as the latter of these functions is almost
identical with that of the other cephalic appendages, it is quite natural, I believe, that,
whereas the males are never seen without these appendages, they are wanting in the
females only of those genera which have also lost their other cephalic appendages.
Finally, it is evident, that the males of those latter genera ought to show the ovigerous
legs in such a rudimentary state, as to be fit only for the ovigerous function.

Dorsally the front part of the cephalothorax bears the oculiferous tubercle ; although

1 Hereafter I will show that this rule admits of an exception. See under Nymphon brevicaudatum, Miers.

16 THE VOYAGE OF H.M.S. CHALLENGER.

in many instances—especially in the true deep-sea species—the eyes are wanting (a
matter to be discussed hereafter), it never happens that the tubercle has totally dis-
appeared. Most genera have this tubercle placed nearly in the middle between the two
ovigerous legs; but in some genera (Phowichilidiwm, e.g.) it is situated much nearer
the front of the segment.

The thoracic part of the cephalothorax and the three following true thoracic segments
are furnished with lateral processes for the insertion of the legs; these lateral processes
in the different genera, and even in different species of the same genus, are of very diffe-
rent lengths. The segments of the body themselves are also of very different lengths.
There are extremely slender forms with long segments and widely separated lateral
processes, and there are also forms so highly concentrated, that the lateral processes
are not separated at all; and between these extremes, which are often met with in one
and the same genus, numerous intermediate forms are to be observed. The dorsal
surface of the body is either smooth or furnished with knots, spines, strong prickles, &c.

At its extremity, between the two lateral processes for the insertion of the last
pair of legs, the last thoracic segment has a rudimentary abdomen of varying length,
which is sometimes (Colossendeis, e.g.) connected with the segment by means of an
articulation, and also sometimes (Zetes, Kréyer) shows traces of bemg divided into
two segments.’ At its extremity the anal aperture is found.

The legs begin at the ends of the lateral processes ; they are eight-jomted. For the
joints I retain the names proposed by Johnston ; these names are the same as those used
in entomology, but it is evident that in this case identity of name does not necessarily
go along with identity of meaning; neither analogical nor homological comparison is
meant by it.

The first three (the coxal) joints are as a rule very short; the following three, the
thigh and the two tibial joints, are much longer (the second tibial being in most cases the
longest of all). The two tarsal joints are again a great deal ‘shorter. The first tarsal
as a rule is shorter than the second; in many instances it is even extremely small, its
function then being only to furnish a highly movable articulation to the last joint of the
leg. At its extremity the last joint is furnished with a claw, which is, or is not, accom-
panied by two accessory claws.” In some genera (Colossendeis, e.g.) accessory claws are
never observed, while in other genera (Nymphon) they occur in some species and are
wanting in others, Therefore the presence or absence of accessory claws alone should
not be made use of in establishing new genera.

1 Rhynchothorax mediterraneus, Cos., Microdoride mediterranea, Napoli, 1861, has a seven-jointed abdomen (Addome
angusto e brevissimo di 7 articoli).

? | think there is not a single reason for calling this claw a ninth joint. At any rate the homology of the claw with its
accessory claws is much greater than that between the claw and the joints of the leg, and, therefore, if the claw is con-
sidered as a ninth joint in those cases where accessory claws are observed, we must speak of a joint having two lateral
joints close to its origin, which would be absurd. ‘

REPORT ON THE PYCNOGONIDA. 17

CATALOGUE OF THE SPECIES OF PYCNOGONIDA AT PRESENT KNOWN, WITH INDICATIONS
.OF THE Hapirat AND RANGE IN DEPTH OF EACH SPECIES.

A point of interrogation has been placed before uncertain or not sutfticiently deter-
mined species, and an asterisk before those dredged by the Challenger Expedition, and
during the cruise of the “ Knight Errant” ; of these a full description is given hereafter.
In the left-hand column the range in depth of each species is given.

Class PYCNOGONIDA, Latr.

Crustacea haustellata, Johnston ; Crustacés aranéiformes M.-Edw. ; Podosomata, Leach ; Pantopoda, Gerstiecker.

Family I. Nympsonip%
Contains those Pycnogonida which have both mandibles and palpi strongly developed.
The ovigerous legs are always present in both sexes, and are, as a rule, furnished with
denticulate spines. The only genus: NMymphon.

Depth in Fathoms. Name. Geographical Distribution.

Nymphon. Fabr. (1794)
Mandibles biarticulate, cheliform ; palpi, five-jointed ; ovigerous legs,
ten-jointed.
A. Species with auxiliary claws.
10 to 15 Nymphon hirtipes, Bell, Belcher, The Last of the Arctic | Lat. 64° 36’, long. 10° 21’ 5”,

(Miers). Voyages, vol. ii. p. 408, 1855. Prof. G. O. Sars Off Halifax ; Franklin-Pierce
33 (Bell). (1877) considers this species to be the same as JN. Bay ; Discovery Bay; Fle-
48 to 50 hirtum, Fabr., which in that case would not be identi- berg Beach; Northumberland
(Wilson). cal with WN. hirtum, Fabr., as described by Kroyer Sound. ‘Appears to be a
52 (U.S. (1845). As it is impossible to recognise the species common inhabitant of the
Fish. Com.). by the description of Fabricius, I think it safest to high northern latitudes ”
299 (Sars). retain the name JV. hirtum for the species of Kroyer (Miers). (A common species
whose description was published long before Sars’ at different stations in the

Prodromus. WV. hirvtum, Fabr., Sars, in Prodromus Barents Sea. Hoek, in MS.)
descriptionis, &c. (Arch. fiir Math. og Nat., ii. 1877).
NV. hirtipes, Bell, Wilson, Pyenogonida of New Eng-
land, Trans. Connect. Acad., vol. v., 1880. Having
received from the U. 8. Fish. Commission a specimen
brought up off Halifax, I feel certain that the animal
described by Wilson belongs to this species. Finally,
I believe that the specimens studied by Miers, and
referred by him to W. hirtum (Arctic Crustacea in
Ann. and Mag. Nat. Hist., 4th series, xx. 108, 1877
belong to this species and not to WN. hirtum, Fabr.
The WN. hirtum, var. obtusidigitwm, Miers, seems to be
an undeveloped female of the same species.
(ZOOL. CHALL. EXP.—PART x.—1881) K 3

18 THE VOYAGE OF H.M.S. CHALLENGER.

Depth in Fathoms. Name.

80 to 90 Nymphon pallenoides, G. O. Sars, Crustacea et Pyeno-
gonida nova, Arch. f. Math. og Naturvid., iv., 1879,
p- 470. Of this species Sars says that it is NV. hirsuto
affine, sed statura minore, &c. Perhaps it is only a
local variety. As Sars does not mention the length of
the auxiliary claws, I feel uncertain whether it is
nearest to NV. hirtipes, Bell, or N. hirtum, Fabr.
(Kroyer).

Nymphon hirtum, Fabr. Entom, Systematica, iv. 417,
1794. WN. hirtum, Chr. Fabr. (1), Kroyer, Bidrag, &e.,
Nat. Tidskr., N. R. i, 113, 1845. The description
of Fabricius being quite insufficient, I retain the
species with the diagnosis of Kroyer. Perhaps J.
hirsutus, Sabine (Appendix, &c., p. ccxxvi, 1824),
belongs also to this species ; according to Kréyer this is
doubtful. WV. hirtum, O. F. Buchholz, Crustaceen der
Zweiten Deutschen Nordpolarfahrt, 1874, ii. 397.
In regard to WV. hirtum, Fabr. Heller (Crust., Pyenogon.,
und Tunicaten der K. K. Ost.-Ung. Nordpol. Exp. in
Denkschr. d. Kais. Akad. d. Wiss., Bd. xxxv., 1875),
it is impossible to determine whether it is this species
or NV. hirtipes, Bell, that was observed.

15 to 65 *Nymphon brevicaudatum, Miers, Ann. and Mag. of Nat.
(Bohm). Hist., 4th series, vol. xvi. p. 117, 1875). Crustacea
25 to 120 of Kerguelen Island, Phil. Trans. Lond. vol. elxviii.
(Challenger), Extra vol., pp. 200-214, 1879, pl. xi. fig 8 WV.

horridum, Bohm, Pyecnogoniden des Museums zu
Berlin, Monatsber, der Kénigl Acad. d. Wiss. zu
Berlin, 1879, p. 175, taf. i. fic. 3-3f Béhm’s suppo-
sition that his WV. horvidum was indentical with Miers’
N. brevicaudatum is true, as has been proved by the

more extensive description with illustrations published
by Miers in 1879 in the extra vol. of the Phil. Trans.
of London. Many specimens of this species were
obtained during the visit of H.M.S. Challenger to

Kerguelen,
10 to 80 *Nymphon stromii, Kr., Nat. Tidskr., N. R., vol. i. p. 111,
(Miers). 1845, Wilson (Pyenogonida of New England, Trans.
35 to 90 Connect. Acad., vol. v. p. 17, 1880) believes that the
(Wilson). NV. gracilipes, Heller (Crust. Pyenog. und Tunic. des
515 to 540 K. K. Oester.-Ungar. Exped. Denkschr. d. K. Ak. der
(“ Knight- Wiss., xxxvi., 1875)—not to be confounded with the
Errant ”). N. gracilipes, Miers, and therefore named by Bohm
110 to 160 (Pyenogoniden des Museums zu Berlin, Monatsb. dur
(Barents Sea, K. A. d. Wiss. zu Berlin, p. 170, 1879) N. Helleri—is
Hoek in very closely allied if it is not identical with this

MS.). species. This is also my opinion, although Heller in his

Geographical Distribution.

Coast of Norway (Saltenfjord).

Norwegian Ocean, Iceland, East
Coast of Greenland (Bohm,
Pyenogoniden des Museums
zu Berlin, 1879) ; East Coast
of Greenland (Nordshannan),
Storfjord (Spitzbergen), Buch-
holz, loc. cit.

Kerguelen.

Coast of Norway? (Kroyer),
North Atlantic (Sars and
“Knight Errant” cruise),
Bareuts Sea (Hoek in MS.),
*“Anverschiedenen Punkten”
(Heller, 7.¢., during the
Austria-UngarianN orth Polar
Exped. of 1873); Fleeberg
Beach, Cape Fraser, Grinnel-
land (Miers), Coast of North

America,Gulf of St Lawrence,

REPORT ON THE PYCNOGONIDA.

Depth in Fathoms.

()

412

540 (* Knight

Errant”)

10 to 45

Name.

diagnosis of his species says ; unguiculi auxiliares nulli

(p. 40). A considerable number of specimens of this

species have recently been dredged (North of Scotland)

during the cruise of the “ Knight Errant.” One of the
commonest species in the northern part of the Atlantic.

(?) Nymphon giganteum, Goodsir, Ann. and Mag. of Nat.
Hist., vol. xv. p. 298, 1845. Goodsir’s description is
not sufficient to determine this species. Wilson
(Pyenogonida of New England, Trans. Connect. Acad.,
vol. v. p. 16, 1880) considers this species as identical
with the JV. strémii of Kroyer. As Goodsir does not
even say whether the body is slender or robust, it is
extremely difficult to ascertain whether or not Wilson’s
suggestion is right.

*Nymphon macronyx, G. O. Sars, Prodromus, Arch. f.
Math. og Naturvid., 1. 365, 1877. I know this
species by the description of Prof. Sars, from a pencil-
drawing he kindly sent me, and feel sure it is a good
species. Recently I had a fair opportunity of becom-
ing acquainted with it, as numerous specimens were
dredged north of Scotland, and forwarded to me by Mr
Murray. As only a very short diagnosis of this
species has been given by Prof. Sars, I will publish
hereafter a detailed description of it.

*Nymphon brevicollum, nu. sp. A fine, well-characterised
species.

*Nymphon brachyrhynchus, n. sp. Asmall but well-char-
acterised species, which seems to abound at a depth of
45 to 120 fathoms.

* Nymphon meridionale, n. sp., shows a certain affinity to JV.
gracilipes, Miers (Ann. and Mag. of Nat. Hist., 4th ser.,
vol. xvi. p. 76, 1875) ; so the latter species may be con-
sidered as a shore-relation of this true deep-sea species.

Nymphon gracilipes, Miers, Ann, and Mag. of Nat. Hist.,
4th series, vol. xvi. p.76, 1875. MV. gracilipes,
Miers, Bohm, Pyen. des Mus. zu Berlin, Monatsb. der
K. Akad. der Wiss. zu Berlin, p. 170, 1879. W.
antarcticum, Miers, Crustacea of Kerguelen Island,
Phil. Trans. Lond., vol. elxviii. Extra vol., p.
200-214, pl. xi, 1879. This species seems to be a
good species. Miers thought it necessary to alter the
name he originally proposed, because in the same year
the same name was given by Heller to an arctic
species. The WV. gracilipes, Heller, being only a
synonym of the WV. *strémii, Kr., I think it best to
retain this name for the Kerguelen species, as was

originally proposed by Mr Miers.

19

Geographical Distribution,

off the Isles of Shoals, off
Halifax (Wilson).

Sea at Embleton, Northumber-
land.

Lat. 62° 44’ 5” N., long. 1°
48’ E. To the north of
Scotland.

South of Halifax, Station 49,
Challenger Expedition.
Kerguelen.

South of Kerguelen Island, lat.
65° 42'S., long. 79° 49’ E.,
Station 43, Challenger Ex-
pedition,

Kerguelen.

1 to 2

60 (Wilson)

220 (Sars)

67 (Hoek in
MS.).

Shore; ‘ ma-
jores etiam
in profundo”
(Oth. Fabr.
Fauna
Groenl)
50,20 to 100
(Wilson)
83 (Chal-
lenger).

540 (“Knight |
Errant”. |

THE VOYAGE OF H.M.S. CHALLENGER.

Name.

*Nymphon fuscum, n. sp. This species too seems to be
closely allied to V. gracilipes, Miers.

*Nymphon longicollum, n. sp. The only specimen of this
true deep-sea species shows very characteristic fea-
tures.

Nymphon gracile, Leach, Zool. Mise., vol., i. p. 45, 1814.
N. gracile, Leach, Johnston, An Attempt, &ec., in Mag.
of Zool., 1837. WN. gracile, Leach, Hoek, Ueber
Pyenogoniden, Nied. Arch. f. Zool., iii, 1877. It
has been suggested by Kroyer that it might be the
same as N. grossipes, O. Fabr., but I prefer to retain
the name of Leach for the species as known by the
description and figures of Mr Johnston and myself,
which is distinct from JN. grossipes, O. Fabr., as de-
seribed by Kroyer.

Nymphon megalops, G. O. Sars (Prodromus descriptio-
nis, &e., Arch. f. Math. og Naturvid., ii. 366, 1877).
Not figured. Prof. Sars kindly sent me a pencil-
drawing, and from this drawing and his Latin diagnosis
I believe the species is nearly related to NV. gracilipes,
Miers.

*Nymphon perlucidum, n. sp. A very well-characterised
species, of which, unfortunately, only one specimen was
dredged by the Challenger.

Nymphon longitarse, Kr., Bidrag till Kundskab, Natur.
Tidskr. N. R., i. 112, 1845, is so nearly related to
NV. mixtum, Kr., that it may, perhaps, be only a variety
of that species, andin that case, of course, of J.
grossipes, O. Fabr.; however Wilson (Pycnogonida
of New England, Trans. Connect. Acad., vol. v.
p. 19, 1880) believes it a good species, readily dis-
tinguished by its extremely attenuated appearance.
From the Barents Sea I got some specimens, which
unquestionably belong to the form described by
Kroyer.

*Nymphon grossipes, Oth. Fabr. (sp.), 1780. Pyeno-
gonum grossipes, Oth. Fabr., Fauna Groenlandica, p.
229, 1780. (3) Phalangium grossipes, Linn., Syst.
Nature, xii. 1027, 1766 (2). (?) Mymphon grossipes,
Fabr., Entom. System. emendata et aucta, tom. iv.
p. 417, 1794 (%). MN. grossipes, Oth. Fabr., Kréyer,
Bidrag till Kundskab, Nat. Tidskr., N. R., i. 108,
1845, NV. grossipes, Oth. Fabr., Wilson, Pyenogon.
of New England, Trans. Connect. Acad., v. 21, 1580.
The species is best known from the descriptions
of Kroyer and Wilson. Three specimens were ob-
tained during the Challenger Expedition, and a single

Geographical Distribution.

Kerguelen.

Off Coast of Chili (Station 298,
Challenger Expedition).

British Seas every where (Leach),
Dutch Coast (Texel) (Hoek).

Lat. 63° 10’ 2” N., long. 4° 59’
6” EF. Lat. 64° 36’ N., long.
10° 21’ 5” EB.

Between Celebes and Halma-
hera.

Coast of Greenland and West
Norway ; off Halifax, St
George’s Banks, lat. 61° 47’
2” N., long. 3° 18’ 5” E.
Barents Sea (Hoek in MS.).

North Sea (Bohm, Pyenogoniden
des Museums zu _ Berlin,
Monatsber. der K. Akad.
d. Wiss. zu Berlin, 1879) ;
Coast of Norway (Kroyer),
Barents Sea (Hoek in MS.),
Northern part of the North
Atlantic (“Knight Errant,”
1880) ; East Coast of Green-
land (Fabricius, Buchholz) ;
North Georgian Islands
(Sabine, Suppl. to the Ap-

REPORT ON THE PYCNOGONIDA.

Depth in Fathoms. Name.

417 (Sars).

(’)

160 (Hoek in
MS).

146 to 180

(G. O. Sars).

160 (Hoek in
MS.).

(2) 25 to 35

one during the eruise of the “ Knight Errant” north
of Scotland.

(2) Nymphon mixtum, Ky., Nat. Tidskr. N. Ri p. 100.
1845. N. mizxtum, Kr., Buchholz, Zweite Deutsche
Nordpolarfahrt, Crust., p. 397, 1874. NV. mixtum, Kr.,
G. O. Sars, Prodromus (Archiy. f. Math. og Natur-
vid., ii. 366, 1877)= NV. grossipes, O. Fabr., Wilson,
Pyenogonida of New England, Trans. Connect. Acad.,
vol. v. p. 20, 1880. Wilson thinks the NV. mixtum,
Kr., is undoubtedly a form of NV. grossipes, O. Fabr. I
also believe it so nearly related to NV. grossipes, that it
may be only a variety. Buchholz writes (Joc. cit., p.
397) :—“ Doch muss ich es dahingestellt sein lassen, ob
die von Kréyer angegebene auf dem Verhaltniss der
Liinge des Tarsus zum Endglied beruhende Artunters-
cheidung ausreichend ist, um diese Art von der vorigen
(N. grossipes, O. Fabr.) zu trennen.”

(2) Nymphon brevitarse, Kr., Nat. Tidskr. N. R., i, 115,
1845. WN. hirsutum, Kr., Grénlands Amfipoder, p. 92,
1838 (Autoritate, Kroyer)= NV. grossipes, O. Fabr.,
Wilson, Pyenogonida of New England, Trans. Connect.
Acad., p. v. 20, 1880. In all probability Wilson is
right when he says N. brevitarse is only a form of N.
grossipes.

Nymphon sluiterii, Hoek, in MS., Pyenogonids of the
first two cruises of the W. Barents. A well-character-
ised arctic species, with extremely small auxiliary
claws, second joint of the palpus longer than third,
first tarsal joint longer than second, with a claw
at the end of the legs, which is not shorter than
the last joint of the leg, and a truncate oculiferous
tubercle.

Nymphon serratum G. O, Sars, Crustacea et Pyenogonida
nova, Arch. f. Math. og Naturvid., iv., 471, 1879. An
extremely characteristic species, with a large spine
dorsally on the first three segments of the trunk.

()Nymphon brevirostris, Hodge, Mennell, Report on Dredg-
ing off the Northumberland Coast and Doggerbank,
British Association Report, p. 119, 1862. A very
unsatisfactorily described species; in all probability
the same as WV. brevitarse, Kr. = WN. grossipes
O, Fabr.

Geographical Distribution.

pendix, &e., p. eexxv. 1824);
Coast of North America, from
the Gulf of St Lawrence, as

far south as Long Island
Sound (Wilson), Challenger
Exped., Station 49, South of
Halifax, U. S. A.

Coast of West Norway (Kréyer),
lat. 63° 10’ 2” W., long. 4°
59’ 6” E. (Sars); East Coast
of Greenland, Spitzbergen
(Buchholz, loc cit.).

Coast of Greenland.

Barents Sea (Hoek in MS.).

South of Spitzbergen, Barents
Sea (Hoek in MS.).

(2) Northumberland Coast, Dog-
gerbank.

22 THE VOYAGE OF H.M.S. CHALLENGER.

ew
Depth in Fathoms. Name. Geographical Distribution.

(2) (1) Nymphon glaciale, Lilljeb., N. glaciale, Lilljeb., | White Sea.
Jarzynsky, Premissus Catalogus Pyenogonidarum in
mari glaciali, Annales de la Société des Naturalistes de
St Petersbourg, 1870. I have never seen a specimen
of it, nor do I know where the description of Lilljeborg
is to be found.

(2) (2) Nymphon femoratum, Leach, Zool. Misc., i. 45, pl. xix. | Channel.

fig. 2,1814. MW. femoratum, Leach, Milne-Edwards,

Hist. Nat. des Crustacés, iii. 534, 1840. NV. femor-

atum, Leach, Johnston, An Attempt &c., Mag. of

Zool. and Botany, i, 1837. In all probability not a

good species: description very insufficient; dilated

thighs are common to the females of almost all the
species.

(2) (?) Nymphon pellucidum, Goodsir, Edin. New Phil. Journ., | Coast of England.

vol. xxxii., 1842. Characterised very insufficiently :

may turn out to be a variety of NV. brevitarse, Kr.

(2) (2) Nymphon spinosum, Goodsir, Edin. New Phil. Journal, | Coast of England.
vol. xxxii., 1842. Like the other species of Goodsir,
NV. spinosum has been described so very insufficiently
that it is not to be recognised.

(?) (?) Nymphon johnstonii, Goodsir, Edin, New Phil. Journal, | Coast of England,
vol. xxxii., 1842. A very uncertain species.
(2) (2) Nymphon minutum, Goodsir, Edin. New Phil. Journal, | Coast of England.

vol. xxxii., 1842. Goodsir’s description is so insuffi-
cient that the species is not to be recognised.

(2) (?) Nymphon longiceps, Grube, 46ster Jahres-Ber. der | China Sea.
Schles. Gesellsch. f. vaterl. Cult. p. 54, 1869. The
description of this species is so insufficient that it is
impossible to recognise it.

B. Species without auxiliary claws.
480 (Station | *Nymphon robustum, Bell, Belcher’s Last of the Arctic ; 60° 2’, 62° 44’ 5”, 64° 36’ N.

56, “ Por- Voyages, vol. ii. p. 409, 1855, Tab. xxxv. fig. 4= WV. lat. ; 6° 11,’ 1° 26’ W. long.,

cupine”), hians, Heller, Crust, Pyenog. und Tunicaten der K. K. 1° 48’ E. long. Barents Sea

412: 299 Oester. Ungar. Nordpol. Exped., Denkschr, d. Wiener (Hoek in MS.) North of

(Sars). Akad. xxxv. p. 41, 1875,=N. abyssorum, Norm., Scotland.

375, 540 Wyville Thomson, Depths of the Sea, p. 129, 1873. I
(* Knight quite agree with G. O. Sars (Prodromus, Arch. for Math.
Errant”). og Naturvid., ii, 3865, 1877), who places N. hiuns,
120 to 160 Heller, and JV. abyssorwm, Norman, as identical with
(Barents Sea, this species. A large and excellent species abounding
Hoek in MS.). in the higher northern latitudes. The largest haul of

Pycnogonids, Mr Murray writes to me, he ever saw
was that in which he got an immense number of speci-
mens of this species (Cruise of the “ Knight Errant”
to the north of Scotland, Aug. 1880).

REPORT ON THE PYCNOGONIDA. 23
Depth in Fathoms. Name. Geographical Distribution.

1100 *Nymphon compactum, n. sp. A well-characterised deep- | East of Auckland (Station 128,
sea species, of which only females—two specimens in Challenger Expedition).
all—have been dredged.

50 Nymphon phasmatodes, Bom, Pyenogoniden des Museums | Cape of Good Hope.

zu Berlin, Monatsb. der K. Akad. der Wiss. zu Berlin,
p- 173, 1879,Taf.1. fig. 2-20. Seemsto be a good species.
1375 to 1600 | *Nymphon hamatum, n. sp. A good and common deep- | Between Kerguelen and Cape of

sea species. Good Hope.

1100 *Nymphon longicoxa, n. sp. A fine well-characterised | East of Auckland (Station 168,
deep-sea species, of which thirteen specimens were Challenger Expedition).
dredged by the Challenger.

2160 *Nymphon procerum, n. sp. A slender deep-sea species, | West of Valparaiso(Station 299,
which is well-characterised yet requires further study. | Challenger Expedition).

Family II. CoLossenDEIDa
Contains those Pyenogonida which have either rudimentary mandibles or no mandibles
at all, strongly-developed palpi and ovigerous legs present in both sexes, and as a rule
furnished with denticulate spines. The genera belonging to this group are very numerous :
Ammothea, Ascorhynchus, Achelia, and Colossenders are typical representatives.

Depth in Fathoms. Name. Geographical Distribution.

Ammothea, Leach (1815).

Mandibles Liarticulate, cheliform, feeble ; palpi nine-jointed; ovigerous legs ten-jointed ;
proboscis pyriform.

(%) Ammothea carolinensis, Leach, Zool. Mise., vol. i. p. 34, | South Carolina.

1815, pl. xiii, Of this species a very good drawing

has been published by Leach.

0 to 5 Ammothea pycnogonoides, Quatrefages, Mémoire sur | Saint Malo (Coast of France).

Vorganisation des Pycnogonides, Ann. d. Se. Nat.

3ime série, Zool., tom. iv., Paris, 1845. I think

this species is closely related to A. longipes, Hodge,

but the descriptions of both authors are so very in-

sufficient that this is not to be made out.

() Ammothea longipes, Hodge, Ann. and Mag., 3d series, | Polperro (English Coast) (St

vol. xiii. p. 114, 1864; Grube, Verhandl. d. Schles. Vaast la Hongue (Grube);

Gesellsch. f. vat. Cultur., 1869-72. The description Roscoff (Grube).

of this species is also quite insufficient; it cannot

be made out whether the species described by Grube is

identical with that of Hodge. The specimen of Grube

is furnished with six-jointed palpi, whence I believe it

not to have been an adult animal. In all probability it

is the same as that described by Quatrefages as A. pycno-

gonoules, Ann. d. Se. Nat., iii. série, Zool., tom., iv., 1845.

24 THE VOYAGE OF H.M.s. CHALLENGER.
ee EEE

Depth in Fathoms. Name. Geographical Distribution, ~

(2) (Deep- Ammothea brevipes, Hodge, List of the British Pycno- | Durham Coast ; Heligoland
water). gonoidea, with descriptions of several new species, (Semper).
Ann, and Mag. of Nat. Hist., 3d series, xiii. 113, 1864.
Very insufficiently described.
(2) Ammothea achelioides, Wilson, Transact. Connect. Acad., | Bay of Fundy (U S. A.).

vol. y. part 1, p. 16, 1880. ‘In general appearance it is

closely similar to Achelia spinosa, Stimpson” (Wilson,

loc, ctt.). No doubt there is a near relation between

the genera Achelia and Ammothea, yet a minute

examination of “adult” specimens of both genera

makes it necessary to consider these genera pro-

visionally as distinet.

Béhmia, Hoek (1880).

Mandibles two-jointed, cheliform ; palpi seven-jointed ; ovigerous legs ten-jointed ;

proboscis conical, entirely bent over to the ventral side.
() Bohmia chelata, Bohn, sp.; Pycnogonum chelatum, Bohm. | (2)
Pyenogoniden des Museums zu Berlin, Monatsb. der
K. Akad. der Wiss. zu Berlin, 1879, p. 192 (pl. ii.
fig. 55d). As the specimen observed by Bohm is
furnished with ten-jointed ovigerous legs, I think there
is not a single reason to consider it as a Pyenogonum
in the larval condition. I therefore propose to form a
new genus for it, and to call it after Mr Béhm.

Phanodemus, Costa (1836).

Mandibles cheliform ; palpi three- or four-jointed ; ovigerous legs (2) ; proboscis conical.

(’) Phanodemus horridus, Costa, Fauna del regno di Napoli, | Gulf of Taranto.
Crostacei et Aracnidi, Napoli, 1838, p- 8. Deserip-
tion of this species extremely insufficient.

(?) Phanodemus collaris, Costa, Fauna del regno di Napoli, | Gulf of Taranto, Gulf of
Crostacei et Aracnidi, Napoli, 1838, p. 8 Also Naples.
described insufficiently.

(*) Phanodemus inermis, Costa, Fauna del regno di Napoli, | Gulf of Taranto, Gulf of
Crostacei et Aracnidi, Napoli, 1838, p. 9. Descrip- Naples.
tion not better than those of the foregoing species.

Rhynchothorax, Costa (1861).

Mandibles cheliform, four-jointed ; palpi eight-jointed ; ovigerous legs (2) ;
proboscis long-ovate.
(2) (?) Rhynchothorax mediterraneus, Cos., Microdoride mediter- | North Coast of Africa.
ranea, Napoli, 1861, p. 8, Taf. i. fig, 102, A very
curious animal, with a short and narrow abdomen of
seven joints. The description, however, is insufficient.

REPORT ON THE PYCNOGONIDA.

25. .

SS EE ee ee

Depth in Fathoms. Name. | Geographical Distribution,
Pephredo, Goodsir (1842),
Mandibles cheliform ; palpi three-jointed ; ovigerous legs six-jointed ; proboscis
short, cylindrical,
(2) Pephredo hirsuta, Goodsir, Edin. New Phil. Journal, | Coast of England.
1842, vol. xxxii. p. 136. The description of this
species as given by Goodsir is very insufficient.
Platychelus, Costa (1861).
Mandibles cheliform ; palpi five-jointed ; ovigerous legs (?) ; proboscis pyriform.
(t) Platychelus sardonicus, Costa, Microdoride mediterranea, | Coast of Sardinia,
Napoli, 1861, p.11. The deseription of the genus and
species is given from a single specimen, and this has
been most probably an immature female,
Oiceobathes, Hesse (1867).
Mandibles small, three-jointed, cheliform ; palpi eight-jointed ; ovigerous legs (?) ;
proboscis conical.
® ()Oiceobathes arachne, Hesse, Ann. d. Se. N atur., 5®™° | Coast of France (Brest).

série, vii. 201, 1867. Description quite insufficient.
Perhaps the genus Oiceobathes isthe same as Ammothea.

Ascorhynchus, G. O. Sars (1877).

Mandibles rudimentary, ¢heliform or not cheliform ; proboscis pyriform, more or less bent
over to the ventral side ; palpi ten-jointed ; ovigerous legs ten-jointed.

Ascorhynchus abyssi, G. O. Sars, Arch. f. Math. og
Naturvid., ii. 367, 1877. This well-characterised
species is (according to Sars) very common in the great
depths of the cold region.

*Ascorhynchus glaber, n. sp. A beautiful and large
Ascorhynchus : not very different from A. abyss, G.
O. Sars, Arch. f. Math. og Naturvid., ii. 367, 1877.

Ascorhynchus ramipes, Bohm (sp.). Gnamptorhynchus
ramipes, Bohm, Sitzber. der Ges. Naturf. Freunde zu
Berlin, 1879, p. 56. Tbid., p. 140.

‘1081 to 1539.

1375

(?)

38 * Ascorhynchus minutus,n.sp. A well-characterised species,
nearly allied to A. ramipes, Bohm.
130 *Ascorhynchus orthorhynchus, n. sp.

A very fine and,
I believe, well-characterised species. .

Zetes, Kroyer (1845).

Atlantic between Iceland and
Norway. Lat. 63° 7' N.,
long. 1° 26’ W.; lat. 68°
13’ 5” N., long. 0° 33’ E.

Between Cape of Good Hope
and Kerguelen.

Enosima (Japan).

Southern Coast of Australia:
off entrance to Port Philip.
Great Ocean North of Admir-

alty Islands.

Mandibles rudimentary, three-jointed ; palpi ten-jointed ; ovigerous legs nine- (nonne
ten- (?)) jointed ; proboscis long-ovate.

Zetes hispidus, Kroyer, Naturhist. Tidskr. Ny Raekke, i.
117,1845. Zetes hispidus, Kroyer, Jarzynsky, Premis-
sus Catalogus, Annales de la Soc. des Natur. de St
Petersbourg, 1870.

(ZOOL. CHALL. EXP.—PART x.—1881.)

(?)

Coast of Greenland, Coast of
Russian Lapland.

K4

26 THE VOYAGE OF H.M.S. CHALLENGER.

ee eeeeeEeEeEeEeEeESESESEOSESESEeEeEe

Depth in Fathoms. : Name, Geographical Distribution.

eee eee a

Parazetes, Slater (1879).
Mandibles rudimentary, two-jointed ; palpi nine-jointed ; ovigerous legs ten-jointed ;
proboscis fusiform.
(2) Parazetes auchenicus, Slater, Annals and Mag. of Nat. | Off Cape Sima (Japan).
Hist., 5th series, iii, 281, 1879. Slater calls the generic
characteristic of Parazetes “distinct.” The description
of the genus and species has been given from a single
specimen, so doubt whether the generic differences from
Zetes or any other closely-allied genus will hold good.

Pariboea, Philippi (1843).
Mandibles rudimentary, two-jointed ; palpi five-jointed ; ovigerous legs nine
_ (nonne ten- (?) ) jointed ; proboscis ovate.

(?) Pariboea spinipalpis, Philippi, Arch. f. Naturg., 1843, ix. | Sorrento (Gulf of Naples).
p. 178. Perhaps the description of this species is not
taken from an adult specimen.

Alcinous, Costa (1861).

Mandibles rudimentary, threejointed ; palpi seven- or nine-jointed ; ovigerous legs
eight-jointed ; proboscis ]ong-ovate.

(2) Alcinous vulgaris, Costa, Microdoride mediterranea, | Mediterranean.
Napoli, 1861, p. 13. This species has, I believe, a
certain resemblance to an Ascorhynchus.

(?) Alcinous megacephalus, Costa, Microd. medit. Napoli, | Gulf of Naples.
1861, p. 14. This species belongs rather to Pariboea,
Philippi, than to Alcinous, Costa.

Achelia, Hodge (1864).

Mandibles rudimentary, two-jointed ; palpi eight-jointed ; ovigerous legs
ten-jointed ; proboscis pyriform.

Low water| Achelia spinosa, Stimpson (sp.). Zetes spinosa, Stimp- | Grand Manan; Eastport, Casco
mark to 17 son. Invertebrata of Grand Manan, 1853, p. 37. A. Bay, off Block Island, &e.
fathoms ; 35 spinosa, Wilson, Pyenogon. of New England, Trans.
fathoms. Connect. Acad. of Arts and Sciences, vol. v. p. 7, 1880.

The differences of A. spinosa, Stimpson, from Hodge’s

A. echinata “seem scarcely sufficient to separate them

as distinct species” (Wilson, loc. cit.).

Low tide to} Achelia echinata, Hodge, British Pyenogonoidea, Ann. and
a few faths. Mag. of Nat. Hist., 3d ser., vol. xiii. p. 115, 1864, A
(Hodge). good description of this species has been given by Grube,

St Vaast la Hougue und seine Meeres—besonders seine

Anneliden-Fauna, Verhandl d. Schles. Gesellsch. f.

yaterl. Cultur, 1869-72, p. 27 (Separatabdruck). Per-

haps identical with A. spinosa, Stimpson, Inverte-

brata of Grand Manan, 1853, p. 37.

Channel Islands, Isle of Man;
Durham Coast, St Vaast la
Hougue, Dutch Coast.

Depth in Fathoms.

(?)

()

5 to 7

Down to 14
fathoms

(Wilson).

3 to 4 fathoms, |

(2)

700

REPORT ON THE PYCNOGONIDA.

Name.

27

Geographical Distribution.

Achelia levis, Hodge, British Pyenogonoidea, Ann. and | Polperro, Cornwall (Hodge),

Mag. of Nat. Hist., 3d ser., vol. xiii. p. 115, 1864.
Bohm (Monatsb. d. K. Akad. der Wiss. in Berl., 1879,
p- 186) refers to the same species a specimen from Ker-
guelen with seven-jointed palpi.

Achelia hispida, Hodge, British Pyenogonoidea, Ann.
and Mag. of Nat. Hist., 3d ser., vol. xiii. p. 115, 1864.
I doubt, whether this species described by Hodge is
indeed a true species.

Tanystylum, Miers (1879).

Mandibles rudimentary, one-jointed ; palpi six-jointed ;

proboscis rounded-conical.

Tanystylum styligerum, Miers, Crustacea of Kerguelen
Island, Phil. Trans. London, vol. clxviii., extra vol., pp.
200-214, pl. xi, 1879. Nymphon styligerum, Miers
(sp.), Ann. and Mag. of Nat. Hist., 4th ser., vol. xvi.,
1875. Most probably this is a good species ; however,
I do not feel quite sure that the two specimens studied
by Miers are really full-grown animals.

Tanystylum orbiculare, Wilson, Pyenogonida of New
England, Trans. Connect. Acad., vol. v. p. 5, 1880.
Whether or not Zanystylum will prove a well-char-
acterised genus, or will turn out to be identical with
Achelia, Hodge, is doubtful as yet.

Nizza (Grube), Kerguelen
(Bohm).

Polperro, Cornwall.

ovigerous legs ten-jointed ;

Kerguelen Island, Observatory
Bay.

Vineyard Sound, and occurs as
far south as Virginia (Wilson,
loc. cit.).

Lecythorhyrchus, Bohm (1879).

Mandibles rudimentary, two-jointed or represented by small knobs ; palpi nine-jointed ;
ovigerous legs ten-jointed ; proboscis cylindrical.

Lecythorhynchus hilgendoryi, Bohm, Monatsb. der K. | Enosima (Japan).

Akad. d. Wiss. Berlin, 1879, p. 187. Corniger hil-
gendorfi, Bohm (sp.), 76¢d. and Sitzungsber. d. Ges.
Naturf. Freunde zu Berlin, 1879,.p. 140. Bohm has
given a good description of this species, Joc. cit.

Lecythorhynchus armatus, Bohm, Sitzungsber. der Ges.
Naturf. Freunde zu Berlin, 1879, p. 140. JZ. hilgen-
dorfi, Bohm, is furnished with rudimentary mandibles
represented by small knobs; Z. armatus, Bohm, with
rudimentary but two-jointed mandibles. There can be
no doubt, however (according to Béhm), that these
species belong to the same genus.

Oorhynchus, Hoek (1880).

Yeddo (Japan).

Mandibles rudimentary, one-jointed ; palpi nine-jointed ; ovigerous legs ten-jointed ;

proboscis broadly ovate.

*Oorhynchus aucklandie, n. sp. Of this very character-

istic Pycnogonid, only a single specimen was dredged
during the voyage of H.M.S. Challenger.

East of Auckland.

28

THE VOYAGE OF H.M.S. CHALLENGER.

Depth in Fathoms. Name. Geographical Distribution.
Colossendeis, Jarzyusky (1870).
No mandibles ; palpi ten-jointed ; ovigerous legs ten-jointed ; proboscis long, cylindrical,
club-shaped or bottle-shaped.
120 to 250 | *Colossendeis proboscidea, Sabine (sp.). Phoxichilus pro- | Coast of Russian-Lapland,

(Jarzynsky),.
110 to 166
(Hoek in MS.
540 (Knight)
Errant”).

boscideus, Sabine, Supplement to the Appendix of Cap-
tain Parry’s Voyage, Zoology, p. ccxxvi. C. borealis,
Jarzynsky, Premissus catalogus Pyecnogonidarum inven-
tarum in mari glaciali ad oras Lapponice rossice et in
mari albo, anno 1869 et 70, Annales de la Soc. des Natur.
de St Petersb., 1870. C. proboscidea, Sabine, G. O.
Sars, Prodromus descriptionis, &c., Arch. f. Math.
og Natury., ii. 268, 1877. A gigantic Pycnogonid of
the higher northern latitudes.

*Colossendeis megalonyz, u. sp. A well-characterised
species. In some respects it resembles the C. pro-
boscidea, Sabine, of the higher northern latitudes ; it
has, however, a much more slender body and longer legs.

Colossendeis angusta, G. O. Sars, Prodromus descriptionis,
&c., Arch. f. Math. og Naturvid., ii. 268,1877. This
species is the slender Colossendeis of higher northern
latitudes.

*Colossendeis leptorhynchus, n. sp. This species seems to
be avery good one. It is easily recognized by its

. extremely long and narrow proboscis, of an almost
cylindrical shape.

*Colossendeis gigas-leptorhynchus. A single specimen of
this form was dredged at Station 158. It shows the
proboscis of C. gigas, whereas the palpi are those of C.
leptorhynchus. In other respects it resembles both
species.

* Colossendeis gigas, n. sp. This seems to be the largest,
not only of the species of the genus Colossendeis, but
of all the different forms hitherto described.

25 Colossendeis kroyerti, Wood-Mason (sp.). Rhopalorhyn-
chus kréyerii, Wood-Mason, A small but very charac-
teristic species of the genus Colossendeis. :

*Colossendeis robusta, n. sp. A beautiful species, easily

to be recognised by the form of its proboscis, &e. ;

| *Colossendeis gracilis, n. sp. The species C. media,

C. brevipes, and C. gracilis, proposed by me, only

show very slight differences. In regard to C. gracilis,

I think it is a very interesting fact, that one of the
specimens is furnished with distinct mandibles.

* Colossendeis media, n. sp. Characterised by the long claws

of the legs, and by the peculiar shape of the last joints
of the palpi.

55 to 120

417

400; 1375;
1600

1800

1375 to 1600

1375 to 1600

2225

North Atlantic. Lat. 62°
44' 5” N., long. 1° 48’ E.
Barents Sea. (Hoek in MS.),
North of Scotland (“ Knight
Errant.”).

Lat. 50° S.: Kerguelen ; be-
tween Patagonia and the
Falkland Islands.

North Atlantic ; lat. 63° 10’ 2”
N., long. 4° 59’ 6” E,

Between Kerguelen and Cape
of Good Hope; West of Val-
paraiso; between Hannover
Isle and Patagonia.

South of Australia at
fiftieth parallel.

the

Between Cape of Good Hope
and Kerguelen; between Juan
Fernandez and Valparaiso.

Andaman Islands (Port Blair).

Kerguelen.

Between Cape of Good Hope |
and Kerguelen.

West of Valparaiso.

Depth in Fathoms.

2650

1250

()

(?)

(3)

Shore.

REPORT ON THE PYCNOGONIDA. 29

Name. y Geographical Distribution.

*Colossendeis brevipes, n. sp. In all probability nearly East of Buenos Ayres,
allied to C. media, Hoek, and C- fgracilis, Hoek.
Perhaps not a distinct species but only a variety.

*Colossendeis minuta, n. sp. A very slender and easily | South of Halifax.
recognized species,

Pasithoe, Goodsir (1842).
No mandibles ; palpi eight-jointed ; ovigerous legs nine- (nonne ten-) jointed,
(?)Pasithoe vesiculosa, Goodsir, Edin. New’ Phil. Journal, | Coast of England,

vol. xxiii., 1842. Description and characterisation of
species and genus insufficient.

Endeis, Philippi (1848).

No mandibles ; palpi seven-jointed ; ovigerous legs nine- (nonne ten-) jointed.
Endeis didactyla, Philippi, Ueber die Neapolitanischen | Naples.
Pyenogoniden, Arch. £. Naturgesch, ix., 176, 1843.
Body ovate, ovigerous legs present. I think this must
be considered as a true representative of the genus
Endeis, proposed by Philippi. Semper (Ueber Pyeno-
goniden, Arb. Zool. Zoot. Inst. in Wiirzburg, i. 281,
1874) considers it as a species of Pasithoe, Goodsir.
But this question cannot be settled without more
detailed descriptions of the forms in question.
())Endeis gracilis, Philippi, Ueber die Neapolit. Pyenog., | Naples.
Arch. f. Naturg., ix. 176, 1843. This species has a
very slender body. No ovigerous legs are mentioned ;
perhaps the eight-jointed palpi are in reality the ovige-
rous legs, and this is a species of Phoxichilus without
palpi.
Discoarachne, Hoek (1880).
No mandibles; palpi five-jointed ; ovigerous legs ten-jointed.

*Discoarachne brevipes, n. sp. A very curious species | Near Cape Town.
with a disciform body and short legs.

Family II. Pattenipaz

Contains those Pyenogonida, which have strongly developed cheliform mandibles, and
either rudimentary palpi or no palpi at all. Ovigerous legs are present in both sexes,
and furnished with denticulate spines (Pallene), or present in both sexes and not
furnished with denticulate spines (some species of Phowichilidium), or present only
in the males (other species of Phowichilidiwm). Two genera: Pallene, Phowxichi-

lidium.

30

THE VOYAGE OF H.M.S. CHALLENGER.

Depth in Fathoms.

Shore.

0 to 3

()

()

38 to 40
(?)

38 to 120

()

(?)

Name.:

Geographical Distribution.

Pallene, Johnston (1837).

Mandibles cheliform ; palpi wanting ; ovigerous legs ten-jointed, present in both sexes, The
last four joints of the ovigerous legs often furnished with denticulate spines.

Pallene brevirostris, Johnston, An Attempt to ascertain
&c., Mag. of Zool. and Bot., vol. i, 1837. P.
brevirostris, Johnston, Grube, Mittheilungen iiber St
Vaast la Hougue, &c., Verhandl. der Schl Ges. f.
vater]. Cultur., 1859. P. brevirostris, Johnston, Hoek,
Ueber Pyenogoniden, Niederl. Arch. f. Zool., iii,
1877. <A well-characterised species.

(1) Pallene empusa, Wilson, Pycnogonida of New England,
Trans. Connect. Acad., vol. v. p. 9, 1880. This
species is so closely allied to P. brevirostris, John-
ston of the European coast, that it must be considered
either as the same, or as a variety of that species.

(2)Pallene chelifera, Clapartde (sp.), Beobachtungen iiber
wirbellose Thiere, p. 103, 1863. Claparéde gives a very
insufficient description of this species, which he con-
siders as a Phowxichilidium. I think it most probable,
that it is closely allied to P. brevirostris, Johnston.

Pallene spinipes, Fabr. Pycnogonum spinipes, Faby.
(sp.), Fauna Grénl., p. 232. Pallene spinipes, Fabr.,
Kroyer, Bidrag til Kundskab, Naturhist. Tidskr., Ny
Raekke, i. 118, 1845. Pallene spinipes, Fabr., Jar-
zynsky, Premissus Catalogus, Annales de la Soc. des
Natur. de St Petersb., 1870.

* Pallene levis, un. sp. A well-characterised Pallene species.

Pallene chiragra, Milne-Edw., Histoire Natur. des
Crustacés, tom. iii. p. 535, 1840. ‘The description of
this species given by Milne-Edw,, doc. cit., is insufficient.
Perhaps it is the same as the species for which I propose
the name P. australiensis. ‘

*Pallene australiensis, n. sp. Perhaps it is this species,
which has been described by Milne-Edwards as P.
chiragra (Hist. Nat. des Crust., iii. 535, 1840).

Pallene grubiit, Hoek. I propose this name for the
species described by Grube (Jahresb. der Schles. Ges. f.
vaterl. Cultur., p. 54, 1869), and which Grube con-
sidered as a species of Phowichilidium.

Pallene longiceps, Bohm, Sitzungsher. der Ges. naturf.

Freunde zu Berlin, p. 59, 1879. A very curious species

_ with rudimentary two-jointed palpi in the male sex.

*Pallene languida, n. sp. Nearly allied to P. longiceps,
Bohm (Sitzungsber. der Ges. Naturf. Freunde in
Berlin, 1869).

Northern Europe (Coast of
England, France, of the
Netherlands).

Vineyard Sound, Noank, Con-
necticut (U.S. A.).

French Coast.

Coast of South Greenland ; White
Coast of Russian-Lapland.

South Coast of Australia.
Australia (Jervis Bay).

South-east Coast of Australia.”

China Sea.

Japan.

Melbourne (Australia),

si
e

Depth in Fathoms.

(!)
(?)

12

(?)

()

191 to 459

Shore.

REPORT ON THE PYCNOGONIDA. 31

Name. Geographical Distribution,

Pallene intermedia, Kroyer, Bidrag til Kundskab, Naturh. | Coast of South Greenland.
Tidskr., Ny Raekke, i. 119, 1845.
Pallene discoidea, Kroyer, Bidrag til Kundskab, | Coast of South Greenland, White
Naturhist. Tidskr., Ny Raekke, i. 120, 1845. Pallene | Sea, Coast of Russian-Lapland,
discoidea, Kréyer, Jarzynsky, Premissus Catalogus, | and North Norway.
Annales de la Soc. des Natur. de St Petersbourg,
1870.
Pallene hispida, Stimpson, Invertebrata of Grand Manan, | Near Eastport, Maine ; off Grand
p. 37, 1853. Pseudopallene hispida, Stimpson (sp.), | Manan.
Wilson, Amer. Jour. of Sc. and Arts, vol. xv. p. 200,
1878, Trans. Connect. Acad., v. 10, 1880. Wilson
considers this species, which is a true Pallene, as repre-
senting a new genus, which he calls Pseudopallene.
But there is no difference in the number of the joints of
the ovigerous legs, and the presence or absence of auxil-
iary claws furnishes by no means a trustworthy ground
for division of the genus. “This species is very similar
to the last (P. discoidea, Kroyer) and a larger number
of specimens may show them to be identical” (Wilson,
ibid.).
Pallene lappa, Bohm, Pyenogoniden des Museums zu | Mozambique.
Berlin, Monatsber. der K. Ak. der Wissensch. zu
Berlin, 182, 1879. I was long in doubt whether this ‘i
species was a true Pallene or a Phowichilidium. I |
have arrived at the conclusion that it is indeed a
Paillene, but a young one, with not quite devéloped
ovigerous legs. .
()Pallene cireularis, Goodsix, Edin. New Phil. Journal, vol. | Scotland.
xxxii. p. 136, 1842. Goodsir’s description is insuffi.
cient. Perhaps this species is nearly allied to P.
discoidea, Kroyer, Bidrag. til Kundskab, Naturhist.
Tidskr., Ny Raekke., i. 120, 1845.
Pallene malleolata, G. O. Sars, Crustacea et Pycnogonida Lat. 72° 27’ to 80° N., long. 5°
nova, Arch. f. Math. og. Naturvid., iv. 469, 1879. | 40! to 20° 51’ B,
Seems to be a species characteristic of the higher
northern latitudes.

_ Phowichilidium, Milne-Edwards (1840).

Basis of the proboscis dorsally covered by the front part of the cephalothoracie segment.
On this front part the oculiferous tubercle is placed. Mandibles cheliform ; palpi
wanting ; ovigerous legs five- to ten- (?) jointed, the last four joints never furnished
with denticulate spines ; in some species present in both sexes, in others only in the
male sex.

Phowichilidium femoratum, Rathke (sp.). Nymphon | Greenland, Russian - Lapland
-femoratum, Rathke, Naturh. Selsk. Skr., v., i. 201, | (Jarzynsky), Norway, Den-

32 THE VOYAGE OF H.M.S. CHALLENGER.

—_—_—_—SsSXSX—_—X——————— eee

Depth in Fathoms. ae Name.

1799. Orithyia coccinea, Johnston, An Attempt, &c.,
Magazine of Zoology and Botany, vol. i. p. 378,
1837. P. femoratum, Rathke, Kroyer, Bidrag til
Kundskab, Naturh. Tidskr. i, 1845; Hoek, Ueber
Pyenogoniden, Niederl. Arch. f. Zool. iii, 1877.
This is the largest of the Phoxichilidiums oc-
curring in the neighbourhood of the shores of the
North Sea. (Ovigerous legs, occurring only in the
males, five-jointed).

(2) ()Phoxichilidium globosum, Goodsir, Edin. New Philos.

Journ., xxxil, 1842. Description quite insufficient,

probably a female of some species or other.

Low water) Phoxichilidium mazillare, Stimpson, Invertebrata of
mark (Wil- Grand Manan, 37,1853. P. mavillare, Stimpson, Wil-
son). son, Pyenogonida of New England, Trans. Connect.

Acad., vol. v. p. 12, 1880. I never saw this species.

Wilson says it resembles P. femoratum of Europe.

It has five-jointed ovigerous legs, wanting in the

female.

Tide-pools. Phoxichilidium minor, Wilson, Pyenogonida ‘of New

England, Trans. Connect. Acad, v. 13, 1880.

Smaller than P. mazxillare, to which it is closely allied.

It has also five-jointed ovigerous legs, wanting in the

female. It may be a dwarf variety of P. mavillare

(Wilson).

(2) ()Phoxichilidium mutilatum, Frey u. Leuckart, Beitrige zur
Kenntniss wirbelloser Thiere, p. 165, 1847. With the

fourth pair of legs rudimentary and one jointed oviger-

ous legs. No doubt the description is taken from an
immature specimen.

30 to 42 *Phoxichilidium fluminense, Kroyer, Bidrag til Kundskab,

(Bohm). Naturh. Tidskr., N. R.,i., 1845. Pallene fluminensis,
7 to 20 Kroyer (sp.), Bohm, Pycnogoniden des Museums zu
(Challenger). Berlin, Monatsber. der Konigl. Akad. der Wiss.,

p. 180, 1869. Dredged during the Challenger Ex-
pedition off Bahia. Ovigerous legs in both sexes,
ten-jointed. ;

7 to 20 *Phoxichilidium insigne, nu. sp. A very characteristic
species, with an extremely slender body armed with
spine-forming knobs. :

(2) Phoxichilidium petiolatum, Kroyer, Bidrag til Kundskab,
(Probably 25 Naturh. Tidskr., i, 1845. Padllene attenuata, Hodge,
to 35.) Report British Association, 119, 1862. After Hodge
(Ann. and Mag. of Nat. Hist., vol. xiii, 3d series, p.
116, 1864). Pallene attenuata is asynonym of Kroyer’s
P. petiolatum. Ovigerous legs seven-jointed, wanting

in the female.

Geographical Distribution,

mark, Heligoland, England,
Holland.

North Atlantic (Orkney).

Bay of Fundy, Casco Bay,
Halifax (East Coast of North
America).

Casco Bay (East Coast of North
America).

Heligoland.

Coast of Patagonia, Magellan
Strait, Coast of Brazil,

Bahia.

Coast of Norway (Oeresund),’
Coast of Northumberland,
Doggerbank. .

REPORT ON THE PYCNOGONIDA. 3333
Depth in Fathoms. Name. Geographical Distribution,
48 to 175 * Phoxichilidium patagonicum, n. sp. A beautiful species. | Patagonia.

' It was dredged at different stations in the neighbour-
hood of the Patagonian coast.

600 *Phoxichilidium patagonicwm, var. elegans, Hoek. | East of Cape Corrientes (La
Whether this is a true variety of the preceding species, | Plata).
or is only to be considered as a young specimen of this
species, I am unable to ascertain.

(4) Phoxichilidium digitatum, Bohm, Pyenogoniden des | Singapore.
Museums zu Berlin, Monatsber. der K. Akad. der Wiss.
in Berlin, 184, 1879. Perhaps nearly allied to my
P. patagonicum (ovigerous legs occurring only in the
males. Number of joints ?).
(2) ()Phouichilidium pygmeum, WHodge (sp.). Pallene | England.
pygmea, Hodge, British Pycnogonoidea, Ann, and
Mag. of Nat. Hist., 3d series, vol. xiii, 1864. As
far as I could ascertain from the extremely insuffi-
cient description of Hodge, and from his figures,
this species belongs to the genus Phoxichilidium.
One of the species of Phowichilidium occurring on the
French and on the Dutch coast is probably the same
species. Should this prove to be true the ovi-
gerous leg is six-jointed and occurs only in the

male.

Shore. Phoxichilidium virescens, Hodge, British Pyenogonoidea, | English Coast —_ (Polperro),
Ann. and Mag. of Nat. Hist., 3d series, vol. xiii., 1864. French Coast (Grube, Mit-
Description insufficient. As far as I could make out theilungen iiber St Malo u.
it is one of the more common forms of the Dutch and Roscoff), 4

French coast. (Ovigerous legs wanting in the female,
six-jointed. ) ;
Tide-marks to | Phowichilidium lentum, Wilson (sp.). Anoplodactylus | Vineyard Sound; Bay of
6 fathoms. lentus, Wilson, Pycnogonida of New England, Trans. Fundy (New England).
Connect. Acad. of Arts and Sc., vol. v. p. 14, 1880.
Wilson gives this name to the species described by
Smith (Report Invertebrata of Vineyard Sound, p. 250)
as Phoxichilidium maaillare. I think it is closely
allied to Phowxichilidium virescens, Hodge (Ann. and
Mag., 3d. ser., vol. xiii. p. 115, 1864). Ovigerous legs
only in the male, six-jointed.
1675 *Phoxiehilidium oscitans, n. sp. A very curious deep-sea | Atlantic: West of Azores.
species, easily to be recognised,
1600 to 1950 | *Phoxichilidium pilosum, nu. sp. A beautiful deep-sea Between Cape Town and Ker

species, guelen; between Kerguelen
and Melbourne.
1875 *Phoxichilidium mollissimum, n. sp. Unfortunately only Off Yeddo (Japan).

a defective specimen of this curious form was dredged
by the Challenger Expedition. It has ten-jointed
ovigerous legs.
(ZOOL. CHALL, EXP.—PART x.—1881.) K5

34 THE VOYAGE OF H.M.S. CHALLENGER.

}

‘Depth in Fathoms. Name. Geographical Distribution.
- (4 Phoxichilidium johnstonianum, White (sp.). “Nymphon | South Seas.

johnstonianum, White, Proc. Zool. Soc. of London,
vol. xv., 1847. There can be no doubt that this species
belongs to Phoxichilidium : eyes situated above the
insertion of the chelicera (mandibles); beak (pro-
boscis) springing from the under side of the head ;
chelicera with two basal joints, &c. The description,
however, is hardly sufficient. What White describes
as palpi are in all probability the ovigerous legs,
(2) (2)Phoxichilidium phasma, White (sp.). Nymphon phasma, | South Seas.
White, Proc. Zool. Soc. of London, vol. xv., 1847.
Whether this species also belongs to this genus or is
to be considered as a Pallene (it is certainly not a
WNymphon) is not to be ascertained. White says it may
possibly be the other sex of the preceding .....

Oomerus, Hesse (1874).

Oculiferous tubercle placed at the base of the proboscis ; mandibles with long pincers ;
palpi represented by small knobs ; ovigerous legs not present in the female.

(1) (1)Oomerus stigmatophorus, Hesse, Ann. d. Sc. Nat. Zool., | Brest (Bretagne).
5®me série, xx., 1874, art. 5, p. 18, pl. viii. In all
probability this is a species of the genus Phowichili-
dium, Milne-Edwards. Only a female without oviger-
ous legs, and with highly developed ovaries in the
fourth joint of the leg, was observed by Hesse.

Family IV. PaoxicHitm

Contains those Pycnogonida, which have neither mandibles nor palpi, or have them
rudimentary. Ovigerous legs, as a rule, only in the males, whereas Hannonia possesses

them in both sexes; always without denticulate spines. Genera: Hannonia, Phowichilus,
Pycnogonum.

Depth in Fathoms. Name. | Geographical Distribution.

Hannonia, Hoek (1880).
Mandibles rudimentary, chelate, two-jointed ; no palpi ; ovigerous legs ten-jointed,
present in both sexes,

Shore. *Hannonia typica, u. sp. A short-legged species, a true
littoral form, with very characteristic features.

Cape of Good Hope.

REPORT ON. THE PYCNOGONIDA. 35

Depth in Fathoms, Name. Geographical Distribution.

Phowxichilus, Latr, (1816).

Mandibles and palpi wanting; ovigerous legs, seven-jointed, present only in the males ;
body, as a rule, slender, :

Shore. Phoxichilus spinosus, Montagu (sp.). Phalangium | Coast of Norway; Coast of
spinosum, Montagu, Linn. Transact., vol. ix. p. 100, Russian-Lapland (Jarzynsky);
pl. v. fig. 7, 1808. PP. spinosus, Montagu, Johnston, England (South Coast of
An Attempt, &., Magaz. of Zool. and Bot.; i. 1837. Devonshire).

Phoxichilus spinosus, Mont., Kroyer, Bidrag til
Kundskab Naturh., Tidskr. Ny. Raekke, i, 1845.
The Phowichilus spinosus, Leach, as described and
figured by Quatrefages (Ann. d. Se. Nat., 3°™° série,
Zool., tom. iv. 1845) is not a Phoxichilus at all.
Perhaps it is a Pallene.

(t) Phoxichilus meridionalis, Bohm, Pyenogoniden des | Singapore.
Museums zu Berlin, Monatsber. der K6nigl. Akad. der
Wissensch. zu Berlin, 1879, s. 189, Taf. ii, fig, 4-46.
A species which stands between P. levis, Grube, and
P. inermis, Hesse (Bohm). ‘

(2) ()Phoxichilus inermis, Hesse, Ann, d. Sc. Natur., 5°™° | French Coast or Mediter-

série, tom. vii. p. 199, 1867. Perhaps nearly allied to ranean (1).

P. levis, Grube. Judging from Hesse’s description, this

species is furnished with a three-jointed abdomen, and

this is not the case with Grube’s species, nor perhaps
with any species of the Pycnogonida. It was taken
at Brest on the keel of a ship returning from the

Mediterranean.

Shore. Phoxichilus lewis, Grube, Mittheilungen iiber St Malo | French Coast.

und Roscoff, 1872. During a recent visit to Roscoff

(Bretagne) I collected specimens of this species, which

is easily distinguished from P. spinosus, Montagu.

(2) ()Phoaichilus pigmeus, Costa (Fowichilus pigmeus), | Gulf of Naples.

Fauna del Regno di Napoli, Napoli, 1836, p. 10.
This species, characterised by its smallness and by the
absence of the spines at the end of the joints of the
legs, is perhaps identical with P. inermis, Hesse, or
P. levis, Grube. Description very insufficient,

Pyenogonum, Briinnich (1764).

Mandibles and palpi wanting ; ovigerous legs nine-jointed, present only in the males ;
body, as a rule, robust.

Tide marks to | *Pyenogonum litorale, Stvém (sp.). Phalangium | North European Coasts and
430 fathoms. litorale, Stro6m, Physisk. og ceconomisk beskrivelse Seas ; Coast of Russian Lap-
over fogderiet Sdndmér, Sorde, 1762. P. Ltorale, land (Jarzynsky) ; Coast of
Strém, Kroyer, Bidrag til Kundskab, Naturh., Tidskr. North America, as far south as
Ny Raekke, i. 126, 1845. P. ltorale, O. Fabr., Long Island Sound ; Coast of

36

| ]
Depth in Fathoms.

THE VOYAGE OF H.M.S. CHALLENGER.

Name.

Wilson, Pycnogonida of New England, Transact. Con-
nect. Acad., vol. v. p. 4, 1880. In the Ann. and Mag.
of Nat. Hist., 5th series, vol. iii. p. 283, 1879, Slater
describes a variety of this species, which, being very
slender, is named P. litorale, var. tenue, Slater. It
was dredged by Capt. St John and placed in the British
Mus. Catal., 78, 11.

Geographical Distribution.

Chili (Gay) ; Mediterranean ;
Japan. The greatest depth
from which it has been ob-
tained in Europe is, as far
as I could ascertain, 53
fathoms (“ Knight Errant”),
whereas it was dredged by

Smith and Harger (1872) at
- adepth of 430 fathoms, east

of St George’s Bank, N. lat.

41° 25’, long. 65° 42’ 3” W.
(4) '(t)Pycnogonum australe, Grube, Jahresb. der Schles. Ges. | Australia.
f. vaterl. Cultur, p. 54, 1869. Of this species only a
larva with three pairs of legs has been examined. It
seems to be a species with auxiliary claws at the ends of
the legs.

DESCRIPTION OF THE SPECIES DREDGED DURING THE CHALLENGER EXPEDITION.
Nymphon, Fabr.

Nymphon hamatum, nu. sp. (Pl. 1.).

Diagnosis.—Body slender, body and legs almost entirely smooth; eyes obsolete,
auxiliary claws wanting; second joint of the palpi longer than the third; second joint
of the leg longer than the first and the third; second tarsal joint of the leg longer
than the first.

Description—tThe body is slender, and the lateral processes are separated. The pro-
boscis is large, almost one-third the length of the body, slightly swollen in the middle,
and again at the extremity. The mouth is triangular, not very large. The cephalo-
thoracic segment (with the base of the mandibles swollen) is almost as long as the
proboscis. The eyes are obsolete, represented only by two small knobs behind the lateral
process of the cephalothoracic segment. The abdomen is rather large; the mandibles
large, with the basal joint as long as the rostrum ; the claws of the chelz are elongated ;
the immovable claw more strongly curved than the movable one (PI. I. fig. 3). _ Both
claws are armed with spines; on the movable claw they are more numerous and larger
(fig. 8). Seen but slightly magnified, the mandibles are smooth ; when greatly magnified
they show small hairs all over the surface.

The palpi are slender, longer than the rostrum ; the second joint is longer than the
third, the fifth longer than the fourth; they increase in length as follows :—First,

REPORT ON THE PYCNOGONIDA. 37

fourth, fifth, third, second. The first and second joints are almost entirely smooth, the
third joint with small and the fourth and fifth with stronger hairs.

The ovigerous legs of the males are stronger than those of the females, and in all the
specimens are bent as shown in the figure (fig. 2). The fourth joint is curved, the fifth
thinner, and much longer than the fourth, and swollen at the extremity ; the sixth is
short, the seventh, eighth, ninth, and tenth very short ; the first joints are sparsely hairy,
the fifth not very hairy, the sixth hairy, with a row of stronger hairs at the outer extremity
of the joint. The spines of the four last joints are not very denticulated (figs. 4 and 5),
their numbers are respectively 12, 10, 9, 12; the end claw is denticulated also. -

In the females the ovigerous legs are shorter, and not bent as in the males. The
fifth joint is only a little longer than the fourth, the sixth joint is less hairy, the
denticulated spines of the four last joints not so numerous, their numbers being
respectively 11, 7, 5, 7. : :

The legs are very long, measuring, for instance, 38 mm. in a female of 11 mm.,
and 44 mm. in a male of 13°5 mm. (1: 3°4, and 1: 3°3); the second joint, which is
swollen at the extremity in the females is longer than the first and third joints;
the fifth joint is the longest, the sixth not much shorter; the second tarsal joint is
longer than the first, the claw is not very strong, nearly half the length of the second
tarsal joint (fig. 9). Auxiliary claws are wanting. The fourth joint of the leg, which
in the females is swollen with the ovary, is furnished at the extremity with a
hook-like process bearing one or two hairs (fig. 8). I believe this is the first species of
Nyinphon, in which this process has been observed, and therefore I have named the species
after it. This fourth segment is furnished in the males with a row of knobs, closed at the
extremity by a thin perforated membrane (fig. 7). Both males and females have the
legs almost entirely smooth, the hairs being so small as to be only visible under the

* microscope. Larger hairs are seen at the extremity of the joints. The last joints are

furnished with small but very dense hairs. The genital openings of the females are
large, and easily observed on the lower side of the second joint on each leg (fig. 6).
Those of the males are a great. deal smaller, and six in number; they are not found
at the first pair of legs. The colour of alcoholic specimens is light yellowish (for the
larvee see below). me

Habitat—tThis very beautiful species was dredged during the Challenger Expedition
between the Cape of Good Hope.and Kerguelen, off the Crozets Islands. There are in
all eight specimens, of which four are males and four females. One of the males was
furnished with eggs, or rather with young ones, adhering still to the accessory legs.
The species was found at two stations, at 1375 and 1600 fathoms. At the same time
were obtained two specimens of Ascorhynchus glaber, Hoek, two of Colossendeis gigas,
Hoek, three of Colossendeis leptorhynchus, Hoek, three of Colossendeis gracilis, Hoek,
and one of Phowichilidium pilosum, Hoek.

38 THE VOYAGE OF H.M.S. CHALLENGER.

Station 146. December 29, 1873. Lat. 46° 46’ S:, long. 45° 31’ E. Depth, 1375
fathoms. Bottom temperature, 1°5° C. Sea bottom, globigerina ooze.

Station 147. December 30, 1873. Lat. 46° 16’ S., long. 48° 27’ E. Depth, 1600
fathoms. Bottom temperature, 0°8° C. Sea bottom, globigerina ooze.

Observations.—Nymphon hamatum is a very fine deep-sea Pyenogonid, and may easily
be distinguished from the other species. Among the described species of Nymphon it
shows some resemblance to Nymphon macronyz, Sars, but this species is a great deal
smaller, has the mandibles and the legs shorter, shows a very prominent and curious-
shaped oculiferous tubercle,! and has the claw of the leg as long as the second tarsal joint.

Nymphon longicoxa, n. sp. (PI. I. figs. 1-5 ; Pl. XV. figs. 8, 9).

Diagnosis.—Body very slender and smooth; legs almost entirely smooth; eyes
small but distinct, oculiferous tubercle rounded ; auxiliary claws wanting ; second joint
of the palpi very long, much longer than the third; second joint of the feet much
longer than the first and the third, the sixth joint the longest, the second tarsal joint
longer than the first. i

Description.—-The body is very slender, the lateral processes with large intervals be-
tween them. The proboscis is large, one-third of the length of the body, in general resem-
bling that of Nymphon hamatum, but alittle narrower. The mouth is triangular, not very
large. The cephalothoracic segment is as in Nymphon hamatun. The eyes are rudimentary,
four, situated on a rounded tubercle. The abdomen is longer than in Vymphon hamatum.

The mandibles are very long, the basal joint longer than the rostrum, the second joint
also very long. The immovable claw, which is curved more strongly than the movable
one, is furnished with very large spines, which reach almost to the extremity (PI. II. fig. 3).
The movable claw furnished with smaller spines has the extremity smooth ; the mandibles
are smooth, the second joint only furnished with microscopic hairs. The palpi are
extremely slender, longer than the rostrum, the second joint is very large, the fourth
and fifth almost equal, the latter furnished with small hairs (fig. 2).

The ovigerous legs of the full-grown males are characteristic. The fifth joint is very
long, and describes an elegant curve; it is divided into two parts by a rudimentary
articulation, and is strongly swollen at the extremity. The sixth joint, which is also
curved, makes an angle with the foregoing. The four last joints are small, and often bent
so as to describe a spiral. The first joints are smooth, at the end of the fifth there is,
on the outside, a small quantity of hairs, the sixth is furnished with numerous hairs, and
has on the upper surface rows of knobs of a curious shape. I have figured some of them
(Pl. XV. fig. 8). They are also present on the fifth joint, but are smaller and not so
numerous. The spines of the four last joints are much denticulated (Pl. II. fig. 4) ; their
numbers are respectively 13,8, 7,6. The spines of the end-claw are very small and blunt.

‘ See the description hereafter in the Appendix.

REPORT ON THE PYCNOGONIDA. 39

The ovigerous leg of the full-grown female is almost entirely straight. The difference
in length between the fourth and the fifth joints is not so considerable ‘as in the males ;
the denticulated spines on the four last joints are more numerous than in the males,
their numbers being 19, 12, 10, 9. These curiously-shaped knobs do not occur on. the
ovigerous leg of the female.

The legs are still longer than those of Nymphon hamatum. In a female of
12 mm. they measured 46 mm.; in a male of 93, 38 mm. (1: 3°8 and1:4). The
second joint is in the males four times as long as the first, in the females a little
shorter, but considerably swollen at the extremity ; the sixth joint is the longest, being
more than once and a half the length of the fifth; the first tarsal joint is shorter than
the second, the claw is almost as long as the first tarsal joint, auxiliary claws are
wanting (Pl. II. fig. 5). The first joints of the legs are almost entirely smooth, the
hairs increasing in number as they approach the extremity of the leg. The genital
openings of the females are very large, and are found on every leg. Those of the
males are smaller, and found only on the three hinder pairs of legs (Pl. XV. fig. 9).
The colour of alcoholic specimens is light yellowish. (For the larvae see below.)

Habitat.—This fine species was dredged east of Auckland. There are in all twelve
specimens, of which only three are females. One of the males was furnished with larvee
clinging to the accessory legs. The depth at which the specimens were found is 1100
fathoms. At the same place two specimens of Nymphon compactum, Hock, were obtained.

Station 168. July 8, 1874. Lat. 40° 28’ S., long. 177° 43° E. Depth, 1100
fathonfs. Bottom temperature, 2°0° C. Sea bottom, grey ooze.

Observations.—I believe this species with its rudimentary eyes to form the transition -
from the shallow-water species to the true deep-sea species. The very long coxe render
the species easily distinguishable.

“Nymphon procerum, n. sp. (Pl. II. figs. 9-12).
Diagnosis.—Body extremely slender, smooth; legs hairy ; eyes obsolete ; auxiliary
claws wanting; the second joint of the palpi a little longer than the third, the second

“joint of the leg longer than the first and the third, the second tarsal joint of the leg a

little longer than the first.
Description.—The body is very slender, and the lateral processes are separated by large
intervals. The proboscis is slender, shorter than one-third of the length of the body, in

‘the middle a little thicker. The cephalothoracie segment is longer than the proboscis.

Eyes are wanting; the abdomen is small and bent upwards. The mandibles are very
long, the basal joint longer than the rostrum, the second joint also long and slender, the
claws very long; the spines of the movable claw are smaller, and closer to one another
than are those of the immovable one (PI. II. fig. 10). The palpi are very slender, much
longer than the rostrum ; the second joint isa little longer than the third ; the fourth and

40 THE VOYAGE OF H.M.S. CHALLENGER.

fifth together are as long, or a little longer than the second joint. The palpi are nearly
hairless, only the last joints being furnished with very small hairs. The ovigerous legs
are feeble, shorter than the length of the body, the fourth joint has a distinct knob at —
a distance of nearly a third of its length, measured from the beginning; the fifth joint is
the longest, the sixth half the length of the fifth, the seventh to the tenth armed-with
sharply denticulated spines (PI. II. fig. 12); the claw has numerous and dense spines
(Pl. II. fig. 11). The ovigerous legs are almost entirely smooth.

The legs are slender, being more than three times as long as the very long and slender
body (body 12 mm., legs 38 mm.). The second joint is longer than the first and third,
and is considerably swollen ; the fourth joint is swollen with the ovaries, and is nearly
as long as the fifth joint, the sixth joint is the longest. The two tarsal joints describe
a slight curve, the second is a little longer than the first, the claw is short, auxiliary claws
are wanting. The fourth, fifth, and sixth joints have long but not very dense hairs; the
seventh and eighth joints have denser but very smal]] hairs. The second joint of each
leg is furnished with a large genital opening.

Habitat.—The single female specimen of this species was dredged West of Valparaiso,
at a depth of 2160 fathoms.

Station 299. December 14, 1875. Lat. 33° 31’S§., long. 74° 43’ W. Depth; 2160
fathoms. Bottom temperature, 1:1° C. Sea bottom, grey mud.

Observations.—There can be little doubt, I believe, that this species is closely allied
to the two foregoing species. Yet I think its extremely slender and elongated form of
body characteristic enough to establish a new species upon it. With the exception
of Nymphon longicollum, dredged from a depth of 2225 fathoms, of all the genus
Nymphon procerum inhabits the greatest depth.

Nymphon longicollum, n. sp. (Pl: TI. figs. 1-3; Pl. XV. fig. 11).

Diagnosis.—Body slender; distance between the insertion of the rostrum and the attach-
ment of the ovigerous legs very great; eyes obsolete, auxiliary claws extremely small.
The second joint of the palpi twice as long as the third, the second joint of the leg three

‘ times as long as the first, the second tarsal joint of the leg nearly as long as the first.

Description.—The body is slender, the proboscis long, and exactly cylindrical ; the .
cephalothoracic segment is much longer than one-third of the length of the body. The
intervals between the lateral processes of the body are very large, they are totally
wanting between the attachment of the ovigerous leg and of the first true leg.
Eyes are wanting, but the conical oculiferous tubercle is very large and acute. The
abdomen is small. :

The mandibles have the basal joint as long as the rostrum, the second joint is
short, and furnished with short claws. The movable claw is a little longer than the
immovable one, the former is curved at the extremity, the latter straight. The spines

REPORT ON THE PYCNOGONIDA. 41

on the claws are not very prominent (Pl. III fig. 3). The two joints are sparsely
hairy, but the hairs of the second joint are longer than those of the first.

The palpi are not very long, and are feeble. The second joint is considerably longer
than the third ; the first and second together are nearly as long as the last three together.
The hairs are much more numerous on the outer joints than on the first two.

The ovigerous legs are not very long. The first four joints are almost entirely smooth,
with the exception of some long hairs at the extremity of the fourth joint ; the fifth and
sixth are hairy when seen through the microscope, the spines of the four last joints are
sharply denticulated, their numbers being respectively 9, 6, 5, 5. On the claw there are
five not very strong spines. The fifth joint of the ovigerous leg is the longest.

The legs are very slender. The length of the body of the single specimen is nearly
6 mm., that of the leg 26 mm. The second joint is three times as long as the third, the
fourth and fifth are nearly equal, the sixth united with the two tarsal joints are as long as
the fourth and fifth together. The first tarsal joint is at the first lee a great deal shorter
than that of the second. In the other legs the difference between the two tarsal joints is
not so considerable ; the claw is half as long as the second tarsal joint. The auxiliary
claws are extremely small (Pl. XV. fig. 11). The legs, when examined with a magnifying
glass of, small strength are quite smooth ; when magnified greatly they show small hairs,
which increase in number and size towards the extremity of the leg (?). The single
specimen of this species brought home by the Challenger is in all probability a male.
The animal is perhaps a young one, as I failed to observe the genital openings.

Habitat.—The specimen was dredged off the coast of Chili.

Station 298. November 17, 1875. Lat. 34° 7’S., long. 73° 56’ W. Depth, 2225
fathoms. Bottom temperature, 1°3° C. Sea bottom, grey mud.

Observations.—This curious species is very easily distinguished by its extremely long
neck and legs, the latter being more than four times as long as the body. From its long
slender neck it bears a certain resemblance to Nymphon longitarse, Kr. It is a true
deep-sea species.

Nymphon compactwm, un. sp. (Pl. I. figs. 6-8 ; Pl. XV. fig. 10).

Diagnosis.—Body stout, sparsely hairy ; eyes obsolete; auxiliary claws wanting.
Second joint of the palpi longer than the third, the second joint of the leg longer than the
first, the second tarsal joint shorter than the first.

Description.—The body is stout, the proboscis thick and swollen a little in the middle,
and again at the extremity ; the length about one-third of the length of the body. The
cephalothoracic segment is short, swollen anteriorly, and constricted in the middle. Eyes
are wanting, the oculiferous tubercle is represented by a blunt knob (fig. 7). The abdomen
is long. The intervals between.the lateral processes of the body are small. The body is

almost smooth, and the lateral processes are furnished with long hairs. The mandibles
(ZOOL. CHALL. EXP.—PART x.—1881.) K 6

42 THE VOYAGE OF H.M.S. CHALLENGER.

are long, the first joint a little curved, and much longer than the proboscis; at the .
ventral side this joimt shows feebly an articulation near the base ; the second is shorter,
but furnished with very long claws, which are curved at the extremity, and both are
armed with almost the same number of spines. The hairs on the mandibles are distant,
the largest quantity being observed on the base of the immovable claw. The palpi are
not very slender, yet a great deal longer than the proboscis; the second joint is the
longest, then follow the third, the fifth, the fourth, and the first, which is the shortest of
all. On the first two joints the hairs are not so numerous as on the last three joints.

The ovigerous legs of the female (the two specimens dredged by the Challenger were
both females) are tolerably long and stout, once and a third as long as the body; the
fourth, fifth, and sixth joints are nearly of the same length, the fourth being the longest,
and the sixth the shortest. The four last joints again are of about the same length, the
claw is slender, its length two-thirds the length of the last jomt. Joints one to four
are almost entirely smooth, with the exception of a row of hairs at the end of the fourth
joint ; joints five and six are furnished with numerous spines, the last four joints showing
hairs only at the distal extremity. The spines of the four last joints (figured on PI. II.
fig. 8) are of a very irregular shape, and not very numerous, their numbers being re-
spectively 10, 8, 5, 7. The spines of the claw are not very strong.

The legs are three times as long as the body (36 mm. in a body of 12 mm.). The
second joint is longer than the first and third, and swollen, as is always the case in the
females. The fourth joint is also very considerably swollen (with the ovaries), the fifth
and the sixth jomts are nearly of the same length, and a little longer than the fourth ;
of the two tarsal joints, which are together nearly two-thirds the length of the sixth joint,
the first is longer than the second (Pl. XV. fig. 10). The claw is half the length of the
second tarsal joint, auxiliary claws are wanting. The fourth joint of the leg is sparsely
hairy, the fifth a little more so, the sixth is very hairy and shows some strong spines at
the extremity, the two tarsal joints are covered with very minute hairs. The genital
openings are large and easily seen.

Habitat.—Of this species two females were dredged along with Nymphon longi-
coxa, east of Auckland.

Station 168. July 8, 1874. Lat. 40° 28’ S., long. 177° 43’ E. Depth, 1100
fathoms. Bottom temperature, 2°0° C. Sea bottom, grey ooze.

Observations.—Nymphon longicoxa and Nymphon compactum were obtained from
a depth of 1100 fathoms. Mymphon longicoxa shows rudimentary eyes, those of
Nymphon compactum are quite obsolete. Mynvyphon longicoxa is one of the most slender,
Nymphon compactum one of the stoutest species dredged by the Challenger. In the one
the auxiliary claws are wanting, whereas small ones are present in Nymphon longicoza,
and in every other respect they are as widely different as two species of the same genus of
Pycnogonids can be. Nymphon compactum shows some relationship to Nymphon stremii,

REPORT ON THE PYCNOGONIDA. 43

Ky., but my species may be readily distinguished by its very short cephalic segment,
the absence of auxiliary claws, of eyes, &c.

Nymphon meritlionale, n. sp. (Pl. IIL. figs. 4-8).

Diagnosis.—Body slender and smooth, legs not very hairy, slender; eyes four,
distinct ; auxiliary claws present ; second joint of the palpi longer than the third ; second
joint of the legs elongated, second tarsal joint of the leg shorter than the first.

Description—The body of this species is slender, the lateral processes are widely
separated with the exception of the lateral process of the first leg, and the small process
of the ovigerous leg. The proboscis is cylindrical, its leneth is almost one-third of the
length of the body. The cephalothoracic segment with the base of the mandibles is
considerably swollen, very large, longer than the two following segments united. The
eyes are distinct, four, placed round a small conical tubercle. The abdomen is small.

The mandibles are very long and robust. The first joint is a little curved, and longer
than the rostrum, the second joint is also large, and furnished with very strong claws
(Pl. III. fig. 5). The movable claw is longer and more deeply curved than the immovable
one ; both are furnished with a row of blunt and strong spines. The immovable claw
shows numerous hairs which are also observed at the base of the movable one. The palpi
are very long, the second joint is the longest, the third reaching farther than the rostrum,
the fourth and the fifth furnished with numerous hairs, and about the same length.

The ovigerous legs are comparatively small in the single specimen dredged by
the Challenger, which I think is a male not yet fully grown. The fifth joint is the
longest; the four last joints are furnished with very numerous denticulated spines,
their numbers being respectively 17, 16, 13, 13. These spines are comparatively small ;

they are elongated, and densely denticulated (Pl. III. fig. 6). The claw is not very long,

and is furnished to the end with a row of short and blunt spines. All the joints of the
ovigerous legs are smooth, with the exception of a few hairs placed at the extremity of
the fourth and tenth joints.

The legs are long and slender; the specimen of 64 mm. shows legs of 213 mm.
The second joint is more than twice as long as the third; the sixth joint is the
longest, the second tarsal joint is shorter than the first (Pl. III. fig. 7), the claw is very
small, the accessory claws are half as long as the claw (fig. 8); longer hairs are placed
at the extremity of every joint, shorter ones cover the outer joints all over, and are a
great deal less numerous on the inner joints. The genital openings I could not observe.

Halitat.—The only specimen was dredged in the Antarctic Ocean, at Station 153.
February 14, 1874. Lat. 65° 42’ S., long. 79° 49° E. Depth of the sea, 1675 fathoms.
Sea bottom, mud.

Observations.—This is the most southern species of Nymphon (of Pycnogonids in
general) hitherto observed. I think this form is closely related to Nymphon gracilipes,

44 THE VOYAGE OF H.M.S. CHALLENGER.

from Kerguelen; yet the two species may easily be distinguished from each other
by the form of the oculiferous tubercle, by the length of the claws of the mandibles,
and by the length of the legs, which are in Nymphon gracilipes, Miers (after Bohm),
five times as long as the body. It is remarkable that this species living at a depth
of 1675 fathoms should have normally developed eyes.

Nymphon grossipes, Oth. Fabr. sp., (Pl. II. figs. 9-12; Pl. IV. fig. 1).
Pycnogonum grossipes, Oth. Fabr., Fauna Greenlandica, p. 229, 1780. »
Nymphon grossipes, Oth. Fabr., Kroyer, Bidrag til Kundskab, Naturh. Tidskr. N. R., vol. i.
p. 108, 1845.
Nymphon grossipes, Oth. Fabr., Wilson, Pycnogonida of New England, Transactions Con-
necticut Acad., vol. v. p. 21, 1880.

Description.—The body of this species is slender and almost smooth, the lateral
processes are widely separated, with the exception of the small lateral processes of the
ovigerous legs, and those of the first pair of true legs, between which no interval is
observed. The proboscis is not very long, cylindrical, a little swollen at the extremity.
The cephalothoracic segment is longer than the rostrum, swollen considerably at the base
of the mandibles. The abdomen is small. The oculiferous tubercle is very prominent,
conical, acute. The eyes are four, large (Pl. IV. fig. 1).

The mandibles have along basal joint, which is longer than the proboscis and narrower ;
the second joint is not very long; the claws are short, not very hairy, but armed with
numerous equi-distant spines (Pl. III. fig. 10). The two mandibles are, in the three
specimens procured, strongly divergent. The palpi are not very slender, nearly one-half
as long as the proboscis, with the second joint not quite as long as the third, and the fifth
longer than the fourth, furnished with numerous hairs at the end of the third joint, on
the fourth, and on the fifth joint.

The ovigerous legs of the males (PI. III. fig. 9) are long, more than one-half longer
than the body, the fourth joint is the longest, the fifth nearly as long, all the joints are
covered with very small perpendicular hairs. The spines of the four last joints are small,
but numerous and elongated, sharply serrated (Pl. IIL. fig. 11), The claw is small, with
numerous thin spines.

The ovigerous legs of the female are much shorter; 8 mm. in a female of 7 mm.
The relative length of the joints is the same asin the male. The hairs are much smaller.
The numbers of the denticulated spines on the four last joints are respectively 18, 17, 16,
14. There are about sixteen very slender and pointed spines at the claw.

The legs are long and slender, nearly five times as long as the body ; a male of 8mm.
has legs of 38 mm. ‘The joints are sparsely hairy, with a row of stronger hairs at the
junction of two joints; the second joint is twice as long as the first; the sixth joint
is by far the longest. The first tarsal jomt is longer than the second, which is armed with

The figures on Plates III. and IV. belonging to this species are marked, NV. armatum, n. sp.

REPORT ON THE PYCNOGONIDA. 45

a row of very strong hairs placed between the thinner ones (fig. 12). The auxiliary claws
are longer than half the length of the claw.

The one female specimen shows large genital openings on the second joint of every
leg ; the two males have the openings a great deal smaller, and only on the six hind legs.
The female is immature. Its length is 7 mm., that of the males 8 mm.

Habitat.—Of this species three specimens were dredged along with Nynphon brevi-
collum, south of Halifax.

Station 49. May 20, 1873. Lat. 43° 3’ N., long. 63° 39’ W. Depth, 83 fathoms.
Bottom temperature, 1°6° C. Sea bottom, gravel, stones.

Observations.—The specimens of this species have long been considered by me as
closely related to, yet distinct from the Mymphon grossipes, O. Fabr. When I first
examined this species, and made the drawings as figured on Plate III., I knew
Nymphon grossipes only by the description of Kréyer. Since that time Mr Wilson’s
paper was published (March 1880), and as soon as I read his description of Nymphon
grossipes, I almost felt sure that he had examined specimens quite identical with mine,
and had rightly considered them as Nymphon grossipes. Lately | have had an oppor-
tunity of comparing the specimens of Nymphon grossipes dredged during the Challenger
cruise with others, undoubtedly belonging to the same species, collected during the two
cruises of the Dutch schooner “ Willem Barents” in the Barents Sea. As there are
however a few differences to be pointed out, it would perhaps be better to consider the
Challenger specimens as forming a variety of this species, yet I hesitate to make such a
proposal, as it is impossible to settle these questions without large collections from the
same, or about the same, localities.

Nymphon brevicollum, n. sp. (Pl. III. figs. 183-15, Pl. XV. figs. 12, 13).

Diagnosis.—Body not very slender; legs slender, smooth; neck short; a small
interval between the attachment of the ovigerous leg and the first true leg ; intervals
between the lateral processes short; oculiferous tubercle blunt ; second joint of palpi
longer than third, second joint of the legs longer than first and third, second tarsal
joint shorter than the first. Auxiliary claws present.

Description.—The proboscis of this species is comparatively large and nearly
cylindrical. The neck is short, yet the segment formed by the conjunction of the
cephalic and the first thoracic segment is tolerably large, there being also an interval
(longer in the females than in the males) between the ovigerous leg and the first true leg.
The abdomen is small. The oculiferous tubercle rounded and small, with four brown eyes.

The mandibles vary considerably ; they often have the first joint shorter than the
rostrum, the second joint comparatively long, the claws long also, armed with numerous
small spines. Those of the males are more slender than those of the females.

The palpi are very slender ; the first and second jomt forming in the females a right

46 THE VOYAGE OF H.M.S. CHALLENGER.

angle with the proboscis. The second joint is very long, much longer than the third.
The fourth and fifth are nearly equal, shorter than the third joint, together nearly as long
as the second. The hairs on the first three joints are few, on the last two numerous,
closely adhering to the joints. The palpi of the males show the same length relatively
to the joints, but they are more parallel with the direction of the proboscis.

The ovigerous legs are slender, only a little longer than the body in the female. The
fourth and fifth joints are nearly of the same length, the sixth shorter. The four last joints
are strongly bent, and describe a spiral. The denticulated spines are long and slender,
their numbers being respectively 17, 14, 11, 13. The claw is very large, and furnished
with numerous small spines (PI. III. fig. 14). The first four joints are almost smooth,
the number of hairs increasing from the fifth to the tenth joint, specially large hairs
being placed at the end of the joints.

In the males the ovigerous legs are a great deal ees nearly 11 mm. when the
body is 6 mm. ; the fourth joint is curved; the fifth forms an angle with the fourth, is
very long, and kare a rudimentary articulation (Pl. XV. figs. 12, 13) at two-thirds of the
length of the joint from the beginning ; the sixth joint is short, but swollen ; the four
last joints and claw as in the female, the denticulated spines being more numerous, and
respectively 19, 16, 12, 15.

The legs of the females are more than four times as long as the body (being 31 mm.
long when the body is 7 mm.). The second joint is considerably swollen, as is the
fourth, which contains the ovary; the fifth joint is longer and thinner than the
fourth, and the sixth than the fifth. The first tarsal joint is longer than the second,
the auxiliary claws are two-thirds of the length of the claw. The fourth and fifth joints
are almost smooth, with the exception of some strong hairs on the fifth joint, and a row
of smaller spines at the extremity. On the sixth joint the number of hairs increases
towards the extremity ; the two last joints have a large number of rather strong hairs.

The leg of a male of 6 mm. is about 25 mm. The leg is a great deal more slender,
especially the second and fourth joints, but the relative length of the joints is the same.
The auxiliary claws of the males are a great deal shorter than those of the females, their
length never reaching half the length of the claw, and often being much shorter. The
genital openings of the females are much larger than those of the males. In the females
they are found on all the legs, in the males they are wanting on the first pair of legs.

Habitat.—With the foregoing species, south of Halifax.

Station 49. May 20, 1873. Lat. 43° 3’ N., long. 63° 39’ W. Depth, 83 fathoms.
Bottom temperature, 1'8° C. Sea bottom, gravel.

Observations. —Of this species eight specimens were dredged by the Challenger. Of
these five are females. Of the three males one is furnished with eggs. These specimens
agree perfectly as to the relative lengths of the joints of the palpi, and of the tarsal
joints of the legs, so that these characteristics are, for this species at least, really dis-

REPORT ON THE PYCNOGONIDA. 47

tinguishing features ; these marks, together with the structure of the first segment of
the body, of the oculiferous tubercle, &c., make this species one of the most sharply-
characterised forms of the genus.

Nymphon brachyrhynchus, n. sp. (Pl. IV. figs. 2-7).

Diagnosis.—Body not very slender, smooth; legs hairy. Proboscis short. Man-
dibles large. Second joint of palpi a little shorter than third. Second tarsal jomt of
the leg longer than first. Auxiliary claws small.

Description—The body of this species is not very slender; yet there are distinct
(but small) intervals between the lateral processes of the body. The proboscis is short,
the segment formed by the conjunction of the cephalic and the first thoracic segment is
also short, as well as the following thoracic segments. The abdomen is comparatively large
and robust. The oculiferous tubercle is small and blunt, the eyes are four in number,
small, and not very distinct, light brown. The body is quite smooth. The length of the
female is nearly 7 mm., that of the male 6°5 mm.

The mandibles are large. The first joint is almost as long as the proboscis, the second
joint curved and long, the claws long also. These claws are curved and furnished with
numerous teeth; they are more numerous and smaller on the immovable than on the
movable claw (Pl. IV. fig.-4). The two claws when closed meet along their whole length,
the tips only crossing for a small extent.

The palpi (Pl. IV. fig. 5) are very slender, more than twice as long as the proboscis.
The third joint is longer than the second, the fourth again longer than the third,
the fifth much more slender, but almost as long as the second. Hairs are scarce on the
second, not very numerous on the third joint, more numerous on the fourth, and very
numerous on the fifth joint.

The ovigerous legs of the males are more than 10 mm. long ; the fourth joint slightly,
the fifth strongly curved and very long, the sixth joint short ; the four last joints are short
and wound up spirally. Small hairs are placed vertically on the fifth and sixth joints,
larger ones at the extremity of the joints. The denticulated spines greatly resemble
those of Nymphon longicoxa, though they are a little flatter ; their numbers are respectively
13, 9, 7, 7. The spines of the claw are small and not very numerous (Pl, IV. fig. 6).

The ovigerous leg of the female is a great deal smaller: a female of 7 mm. in
length, has ovigerous legs of 8°5 mm. The fourth and the fifth joints especially are much
shorter, and the latter are quite straight. The denticulated spines of the four last joints
are more numerous than in the males; they are 14, 12, 10, 9, which numbers, however,
vary slightly for the different specimens. The claw with its spines is like that of the male.

The legs are slender, those of a male of 6°5 mm. nearly 25 mm., those of a female of
7 mm. nearly as long (25°5 mm.). The second joint is more than thrice as long as the third,
the fourth and the fifth nearly of the same length, the sixth almost once and a half the

48 THE VOYAGE OF H.M.S CHALLENGER.

length of the fifth. The two tarsal joints, of which the second is longest, describe a slight
curve ; the claw is large, the auxiliary claws are very small (Pl. IV. fig. 7). Beginning
at the fourth joint the number of hairs regularly increases down to the end of the leg.

The legs of the females show the second and fourth joints considerably swollen. In
the females the genital pores are large, and to be found on every leg ; in the males they
are much smaller, and occur only on the two hind pairs of legs. |

Habitat.—A large number of specimens of this species was gathered in Christmas
Harbour, Kerguelen. There are a great number of females with the ovaries swollen in
the fourth joint of the leg; a great many males with and without eggs or larve on their
ovigerous legs.

The specimens were dredged at a depth of 45 to 120 fathoms. (January 29, 1874.
Off Christmas Harbour. Depth, 120, 105, and 45 fathoms.)

Observations.—This fine species shows very characteristic marks, and cannot easily
be confounded with other species. In some respects it shows a resemblance to Nymphon
strani of Kroyer.

Nymphon fuscum, n. sp. (Pl. IV. figs. 8-11).

Diagnosis.—Body and legs very slender. Cephalic segment of the body large,
occasioned by the length of the so-called neck. Second joint of the palpi the longest ;
second joint of the leg three times as long as first; tarsal joints of leg nearly equal.
Accessory claws present.

Description.—In this species the body is again extremely slender. The proboscis is
short, the mouth small. Of the cephalothoracic segment the so-called neck is long, the
segment itself is not very long, there being no interval between the ovigerous leg and
the first true leg. Between the true legs the intervals are, on the contrary, very great.
The abdomen is minute. The eyes are very large, covering almost the entire surface of
the short and blunt oculiferous tubercle.

Of the mandibles, the first joint is longer than the proboscis, the second is compara-
tively short, and so are the claws. The movable claw is a great deal more slender
than the immovable one, the latter is furnished with larger teeth, which are not so acute
as the smaller ones of the movable claw (PI. IV. fig. 9).

Of the palpi the second joint is the largest, the fourth the shortest (Pl. IV. fig. 10).
The last joimts are extremely hairy, but hairs are also to be found on the second and
third joints. The palpi are not very long, but stout; their length being about one-
half the length of the proboscis.

The ovigerous legs of the males are very characteristic, forming a very elegant curve.
The fifth joint is the longest and the most strongly bent, the sixth joint is a great deal
shorter, the four last joints are very short ; the claw is short and furnished with very
rudimentary teeth (Pl. IV. fig. 11). The spines of the four last joints are very slender,

REPORT ON THE PYCNOGONIDA. 49

but they are almost all broken at the extremity, their numbers are respectively 14, 14,
13, 13. On the fourth joint hairs are scarce, on the fifth there are a great many small
hairs vertically implanted on the surface of the joint, the hairs of the sixth and the four
last joints are also numerous: they are larger than those of the fifth joint.

The legs are very slender: ina male of 8 mm. their length is nearly 32 mm. The
second joint is more than twice as long as the third, the fifth joint is only a little longer
than the fourth ; the sixth is once and a half as long as the fifth. The two tarsal joints
are nearly equal. The claw is short, being one-third the length of the last joint of the leg.
The accessory claw is not half as large as the claw. The first joints of the leg are
nearly ‘smooth, but from the sixth to the eighth they are covered with very small
rough hairs.

The colour of this species is a dark brown, much darker than is the case with the
other species.. There are in all three specimens, of these two are mature males (one fur-
nished with eggs), the third is a very smal] one with broken accessory legs. I consider
it a young male. Genital pores I observed only on the second joint of the two last legs.

Habitat.—This species was found off Kerguelen Island at a depth of 25 fathoms.

Station 149. January 17, 1874. Lat. 49° 40’ S., long. 70° 28’ E. Off Royal
Sound. Depth, 25 fathoms.

Observations.—This species shows a certain resemblance to Nymphon gracilipes,
Miers. Yet there are too many small differences for me to feel justified in consider-
ing the two forms as identical. The form of the oculiferous tubercle is not as figured
by Bohm, the claws of the mandibles are shorter and not so straight as in Nymphon
gracilipes, Miers (after Bohm, Pycnogon. des Museums zu Berlin, Monatsb. der K.
Akad. der Wiss. zu Berlin, p. 170, 1879) ; the length of the fourth joint of the accessory
legs is different,’ the length of the two tarsal joints, of the claw, the colour of the whole
animal, so characteristic in my Nymphon fuscum, is quite different from that described
by Bohm (fast weiss bis hellbriunlich, Bohm, Joc. cit., p.. 172). There can be little
doubt, however, that these two forms are closely allied.

Nymphon brevicaudatum, Miers (Pl. IV. figs. 12, 13, Pl. V. fig. 1-5. — Nymphon
hispidum, un. sp., is marked on the plates).

Nymphon brevicaudatum, Miers, Ann. and Mag. of Nat. Hist., vol. xvi. p. 107, 1875 ; Crustacea of

Kerguelen Island, Phil. Trans. Lond., vol. clxviii. (extra vol.) pp. 200-214, pl. xi. fig. 8, 1879.

Nymphon horridum, Bohm, Pyenogoniden des Museums zu Berlin, Monatsber. der K. Akad.
der Wiss. zu Berlin, 1879, p. 172, taf. i. fig. 3-37.

Description.—The body of this species is very robust, and has the lateral processes
scarcely separated. The proboscis is comparatively short and bears a small mouth ; the
1 Bohm, loc. cit., taf. i. fig. 1d, represents the sixth joint of the ovigerous leg as furnished with denticulated spines. Of
course this is a mistake.
(ZOOL. CHALL. EXP.—PART x.—1881.) K7

50 THE VOYAGE OF H.M.S. CHALLENGER.

first segment of the body is considerably swollen at the base of the mandibles, constricted
posteriorly, and shows a faint line at the beginning of the first true thoracic segment.
The abdomen is comparatively long. The upper surface of the body is armed with
numerous spines, forming in the middle of the segments star-like groups (Pl. IV. fig. 12),
and scattered more irregularly on the lateral processes; near the end of these a row
of stronger spines is observed. The oculiferous tubercle is, especially in the females,
highly elevated, and shows four dark eyes separated by a cross-like spot. The oculiferous
tubercle is placed on the cephalic part of the first segment, between the two ovigerous
legs.

The mandibles are very long, the first joint being much longer than the proboscis; °
the second joint is shorter and strongly curved, the claws being placed almost trans-
versely before the mouth. The immovable claw is more strongly curved than the
movable one; the spines on the claws are numerous, but they are almost equal and of
the same length. Both joints are covered with numerous small hairs, stronger ones being
found at the end of the first joint (Pl. V. fig. 2).

The palpi are not very hairy. The second joint is by far the longest, the fourth is
the shortest, the fifth very slender. The whole length of the palpus is about twice the
length of the proboscis (PI. V. fig. 1).

The ovigerous legs of the males are not quite so long as the body. The fifth joint
is the longest, and is considerably swollen at the extremity, the sixth joint is a great deal
shorter, the seventh to the tenth joints are very short, the claw almost of the same length
as the last jomt. The ovigerous legs are very strongly bent and not very hairy. The
denticulated spines of the four last joints are sharply serrated and not numerous, their
numbers being respectively 3, 3, 2, 3 (Pl. V. figs. 3, 4). The claw is furnished with a
row of acute spines.

The ovigerous legs of the females are still shorter than those of the males, The -
relative length of the joints is the same, but the fifth joint is not swollen at the
extremity. The leg is not curved as is the case with that of the male.

For a species of Nymphon the true legs are uncommonly short: a female of 6 mm. .
has a leg of only 14 mm. The second joint is not quite twice as long as the first or
third, the three following joints are almost of the same length and comparatively robust,
especially the fourth joint of the female. The two tarsal joints, the second of which is
the longer, are very slender and almost smooth, together about as long as the sixth joint.
The claw is about as long as one-third of the length of the second tarsal joint, the auxiliary
claws are very small. The legs are very hairy. These hairs vary greatly in size and
strength, and are not placed in regular rows. The dorsal surface of the leg especially is
covered by a large quantity of stronger spines. The genital pores of the females are very
large and visible on the second joint of every leg. Those of the males are small, and
found only on the second joints of the two last legs.

REPORT ON THE PYCNOGONIDA. 51

I wish to point out as a very interesting peculiarity of this species, that I observed a
female specimen with highly developed ovaries in the fourth joint of its legs, which bears
a distinct egg-mass on its ovigerous leg. The shape of the ovigerous leg is almost
identical with that of a male. In other respects it looks quite like a female.

Habitat.—This species seems to abound in the neighbourhood of Kerguelen Island.
Miers (oe. cit., p. 213) only says that several specimens were collected at this island, but
Bohm (loc. cit., p. 177) mentions specimens collected in Royal Sound, Irish Bay, and
Great Whale Bay, from a depth of 15 to 65 fathoms.

The Challenger brought specimens home from Station 149. J anuary 17,1874. Lat.
47° 40’S., long. 70° 20’ E. Off Royal Sound. Depth, 25 fathoms.

January 20,1874. Royal Sound. Depth, 28 fathoms.

January 29,1874. Off Christmas Harbour. Depth, 120 fathoms.

Observations.—After a close examination of the numerous specimens of this Pycno-
gonid, I at first believed it to be different from the N’ ymphon horridum of Bohm, so I gave
it the name Nymphon hispidum, which name is still to be found on Plates IV. and
V. of this Report. After a renewed examination, and having acquired, I believe, by
continuous study some knowledge of the relative value of characteristic marks, I think
there can be no doubt about the identity of Béhm’s species and the specimens brought
home by the Challenger. Unfortunately the two plates are printed off, and thus bear
the name originally proposed by me.

However, the name proposed by Béhm ought also to give place to another, viz,
that of Miers. The description of Mr Miers originally published was too short and insuf-
ficient, therefore Mr Bohm was quite justified in considering his specimens as distinct
and proposing for them the new name Nymphon horridum. This happened in 1879.
In the same year Mr Miers published a more detailed description with figures, which
made it certain that Bohm’s, Miers’, and my specimens belonged to the same species ; this
must, I think, bear the name originally applied to it by Mr Miers. -

The latest description of this author, however, is by no means exhaustive ; his figures
are very small, and when he says that the number of claws at the end of the leg is two,
it is evident that he has not studied the details with a high enough power.

Bohm’s description and drawings are much superior to those of Miers ; they differ
from mine in the following respects :—On the dorsal surface of the body he figures rows of
hairs between the different segments, whereas I observed star-like groups of hairs. He
gives the mandibles a much more elongated form, and furnishes the claws with very
irregular teeth. On the legs, Bohm says, the hairs and spines are arranged in regular
rows, whereas I failed to observe this regularity. The two tarsal joints as figured by
Bohm are nearly of the same length, but I always observed that the second was much
longer than the first. Minor differences in the form of the eyes, distribution of the hairs,
&c., it is unnecessary to discuss. The more important ones which I have pointed out

52 THE VOYAGE OF H.M.S. CHALLENGER.

must perhaps partly be attributed to inaccuracy ; they may have been occasioned by the
circumstance that Béhm’s material was much more limited than mine. Bohm doubts
whether he has a male example or not, whereas I had a dozen at my disposal, five of
which were furnished with eggs.

Nymphon perlucidum, n. sp. (Pl. V. figs. 6-10).

Diagnosis.—Body and legs very slender, pellucid and smooth. Second joint of the
palpi elongated, much longer than the third. Second joint of the feet more than twice as
long as the third. First tarsal jomt uncommonly short. Accessory claws.

Description.—This is a very small and a very fine species, the most transparent
form of Nymphon I ever observed. The proboscis is robust, yet very long, much longer
than the first segment of the body. There is no interval between the lateral process
of the ovigerous leg and that of the first true leg, but the intervals between the other
lateral processes are very large. The abdomen is small. The eyes are obsolete: a very
small tubercle without pigment is all that is to be seen.

The mandibles have the first jomt as long as the proboscis, the second small with
very long claws, the immovable claw is strongly curved at the extremity. The number
of spines on these claws is much more limited than in any of the other species of
Nymphon, being four on the movable claw and only five on the immovable one.
The mandibles are scarcely hairy: a few stronger hairs are observed at the end of the
first joint, and again at the origin of the movable claw.

The palpi are not very long, once and a third as long as the proboscis. They are
slender, the second joint being comparatively much longer than the third joint, and
nearly as long as the three last joints together. They are covered with very small hairs.

The ovigerous legs are short: 44 mm. in a male of 5 mm.; the fifth joint is the
longest, considerably swollen at the extremity ; the sixth is a great deal shorter and
feebly bent; the four last joints are very short, the claw being half the length of the last
joint. The different joints are covered all over with very minute hairs. The spines of
the four last joints are broad, but very small and almost show the hand form (PI. V.
fig. 9). They are not very numerous, their numbers being respectively 7, 4, 4, 5. The
claw is furnished with some small spines (PI. V. fig. 8).

The legs are slender, but not very long, only two and a half times as long as the
body. The second joint is twice as long as the first and third; the fifth is longer than
the fourth, and the sixth is the longest. The two tarsal joints are highly characteristic
on account of the shortness of the first, and the strong spines placed along that side of
the second which is opposite the claw. *The length of the accessory claws is not half the
length of the claw. The legs are covered with small hairs, stouter ones being placed on
the fifth and sixth joints, and at the end of the joints. I have figured the two tarsal
joints in fig. 10, Plate V.

REPORT ON THE PYCNOGONIDA. 53

The only specimen of this species collected by the Challenger is a male furnished with
genital pores on the second joint of the two last legs.

Habitat.—This small species was dredged during the Challenger Expedition between
Celebes and Halmahera.

Station 196. October 13, 1874. Lat. 0° 48’ S., long. 126° 58’ E. Depth, 825
fathoms. Bottom temperature, 2°4° C. Sea bottom, rock.

Observations.—This fine species is highly interesting, being among the slender
species of Nymphon, the only one in which the form of the two last joints of the leg
shows a remarkable likeness to that of the same joints of most other genera of Pyeno-
gonida. This, however, is not the only characteristic point ; a second is that the claws
of the mandibles are not armed with a row of very numerous spines as in the other
species of Nymphon, but only with three, four, or five spines. The species is blind, yet
the depth from which it was brought up was only 825 fathoms, whereas Nymphon
meridionale, Hoek, e.g., lives at a depth of 1674 fathoms and has four distinct eyes.

Ascorhynchus, G. O. Sars.

Ascorhynchus glaber, un. sp. (Pl. VI. figs. 5-9; Pl. XV. fig. 16).

. Diagnosis—Proboscis one-third of the total length of the body. Abdomen half as
long as the proboscis, Body and legs almost entirely smooth, with the exception of three
strong spines placed dorsally on the hinder margin of the first three thoracic segments.

Description.—
Length of the proboscis, . - 5 : : : : 83 mm.
Length of the trunk, : ‘ : : : : é 133 ,,
Length of the abdomen, . . : : ; : : ya ete
Total length of the body, . : : : 4 c - 26s,
Length of the cephalothoracic segment, . : . : . ges
Length of the third leg, . ; ; ; : : : BY). es

The body of this beautiful species is strong, yet comparatively slender, with great
intervals between the lateral processes. The proboscis is very stout, pyriform, distinctly
triangular in transverse section ; each of the three sides of the proboscis is longitudinally
furrowed in the middle; at its extremity the proboscis is sharply pointed, the mouth is
small and triangular. The proboscis is distinctly divided into a fore, middle, and hinder
part, the latter tapering towards the extremity, where it articulates with the cephalo-
thorax (Pl. XV. fig. 16). The length of the cephalothoracic segment is very con-
siderable, being about half that of the trunk. Anterior to the insertion of the palpi it is a
little narrower, and at the front part it bears the mandibles, between which it shows
a small azygous knob. On the dorsal surface a slight elevation is observed between the
two palpi, whereas behind the middle, almost exactly between the two ovigerous legs, the

54 THE VOYAGE OF H.M.S. CHALLENGER.

same surface bears a very high conical oculiferous tubercle, which as a sense organ is
quite rudimentary, being destitute of lenses, pigment, &c. A second dorsal conical
elevation is found at the hinder margin of the cephalothorax, and similar very strong
spines are also observed at the hinder margin of the two following thoracic segments
(Pl. VI. fig. 5). At the point where these thorns arise the segments are a great deal
wider than the anterior part of the following segment. The abdomen is comparatively
long but very narrow, being only a little swollen at the extremity. The lateral pro-
cesses for the attachment of the ovigerous legs are short, those for the true legs
comparatively very long.

Both specimens of this species brought up by tha Challenger are furnished with
three-jointed mandibles. Those of the younger specimen bear at the extremity of the
third joint slender and curved claws (Pl. VI. fig. 7); the older specimen, on the
contrary, shows rudimentary straight and very small claws, the movable claw being
furnished with a slender thread (Pl. VI. fig. 6). The latter specimen is a male, and
there is no reason why it should not be considered as full-grown.

The form of the palpi is nearly the same as in the other species of Ascorhynchus.
The first two joints are extremely small, the third is the longest, the fourth is short, the
fifth about twice as long, and narrow in the middle, the sixth is very short; of the seventh
to the tenth joints, the first is the shortest, the second the longest. With the exception
of some extremely small hairs on the last joints, the surface of the palpi is quite smooth.

The ovigerous legs have the fourth joint the longest, the fifth shorter and swollen
towards the extremity, the sixth about half as long as the fifth and yet more
swollen towards the extremity ; of the four last joints the first is the longest, and the claw
at the end of the tenth joint is extremely small. The denticulated spines are placed in
different rows, each row showing spines of about the same size, whereas those of different
rows vary greatly (Pl. VI. fig. 8).

Of the legs the first pair is a great deal less developed than the three following ; its
total length is only 30 mm., whereas that of the third pair is fully 39 mm. Of the latter
leg the second joint is twice as long as the first or third joint, the fourth joint is the
longest, the fifth joint is a little shorter than the fourth, the sixth again a little shorter
than the fifth ; of the two tarsal joints the first is a little shorter than the second, the
claw is not quite half as long as the second tarsal joint. There are no accessory claws
(Pl. ‘VI. fig. 9). The claw of the first leg is extremely minute, yet distinct. The legs
are almost hairless; yet the fourth and the fifth joints cannot be called smooth, as
they are furnished with rows of knobs, corresponding with the knobs I observed on the
lee of Mymphon hamatum, Hoek.

The animal from which all the above measurements, &c., are taken is a male; its
genital orifices are found ventrally on the second joint of the two posterior legs. Its
colour is a beautiful orange-yellow.

REPORT ON THE PYCNOGONIDA. 55

Habitat.—This interesting species was dredged during the Challenger Expedition at
Station 146. December 29, 1873. Lat. 46° 46’ S., long. 45° 31’ E. Depth of the sea,
1375 fathoms. Bottom temperature, 1°5° C. Sea bottom, globigerina ooze.

Observations.—This species is, I believe, closely allied to Ascorhynchus abyssi,
G. O. Sars. It can, however, easily be distinguished from that species.

1. By the proboscis, which is as long as the trunk in Ascorhynchus abyssi, and only
two-thirds the length of the trunk in Ascorhynchus glaber.

2. By the lateral processes of the body, which in Ascorhynchus abyssi, “ vix,” in
Ascorhynchus glaber ave visibly longer than the breadth of the body.

3. By the oculiferous tubercle, which in Ascorhynchus abyssi is denticulate and
placed on the fore part of the first segment, while in Ascorhynchus glaber it is behind the
middle of the cephalothorax and quite smooth.

4. By its three-jointed mandibles.

5. By the legs, which are covered with short hairs and-are twice as long as the body
in Ascorhynchus abyssi ; in Ascorhynchus glaber, on the contrary, they are almost smooth,
and are only once and a half as long as the body.

6. By the length of the body, 10 mm. in Ascorhynchus abyssi, and 26 mm. in
Ascorhynchus glaber.

Ascorhynchus minutus, n. sp. (Pl. VI. figs. 10-16).

Diagnosis.—Proboscis not quite one-third of the total length of the body. Abdomen
one-third the length of the proboscis. Body and first joints of the legs furnished dorsally
. with numerous strong spines.

Description.—

Length of the proboscis, : ; : 5 : : - 2 mm.
Length of the trunk, ‘ : , : : ; ‘ BID) op
Length of the abdomen, ; : . : F : : 0:65 ,,
Total length of the body, . : ; ; : sae a. 64 ,,
Length of the cephalothoracic segment, : . ; : 5 23
Length of the third leg, ; ; ‘ ; i 3 : 9:0)

The body of this nice little species is slender, and the intervals between the lateral
processes are great (Pl. VI. fig. 10). The body and legs are almost entirely smooth, single
hairs being found only at the distal extremities of the joints of the legs. The proboscis
is triangular, almost of the same form as that of Ascorhynchus glaber; it is distinctly divided
into three parts, the middle part being considerably swollen. The cephalothoracic seg-
ment is comparatively long, being as long as the remaining part of the body including
the abdomen. The oculiferous tubercle is situated in front of the middle of the cephalo-
thoracic segment and is much elevated; the eyes are rudimentary. A distinct knob is

56 THE VOYAGE OF H.M.S. CHALLENGER.

to be seen at the front margin of the segment between the origin of the two mandibles.
The three following thoracic segments are short; the two middle segments are
furnished like the cephalothoracic segments dorsally at their hinder margin with an
elevated prickle. The lateral processes which serve for the insertion of the legs, are of
considerable length ; at their extremities they bear a strong prickle, which is not quite
so long as those on the middle of the dorsal surface.

The mandibles consist of a single joint, bearing at its extremity a rudimentary
triangular second joint.

The palpi are slender and comparatively long; the first two joints are extremely
small, the third joint is the longest ; the relative length of the other joints is nearly the
same as in the palpi of Ascorhynchus glaber. The distal extremity of the fifth joint and
the whole surface of the four following joints show on the one side numerous hairs
of the curious form observed and described by Béhm for Ascorhynchus ramipes,
Bohm (sp.) (Gnamptorhynchus. ramipes, Bohm) (Pl. VI. fig. 16).

The ovigerous legs are comparatively short, 5 mm. in the specimens of 6°4 mm, The
first joint is very small, the two following are a little longer, the fourth and fifth are
very long, the sixth a great deal shorter; the four last joints (Pl. VI. fig. 12) are very
short, and about the same length, the claw is not so extremely short as in Ascorhyn-
chus glaber. The denticulated spines are placed in three distinct rows (Pl. VL. fig. 13).

The first joints of the legs are furnished dorsally with strong prickles, like those of the
dorsal surface of the body and the lateral processes. The first joint of the leg is furnished
with two, the second joint, which is but little longer than the first, with a single prickle.
On the third joint, which is nearly as long as the first; no prickles are to be seen. The
fourth is shorter than the fifth ; the latter, the longest of all, is also a little longer than
the sixth joint. Of the two last joints the first is a little shorter than the second (Pl.
VI. fig. 14). The claw is longer than half the length of the second tarsal joint.
Accessory claws are wanting. The first pair of legs, which is much feebler than the
three following pairs, has a very small claw (Pl. VI. fig. 15).

Both specimens of this species collected during the cruise of H.M.S. Challenger are
males. I observed small genital pores on the two hinder legs at the place which, as
far as my knowledge goes, they invariably occupy. One of these males bears larvee,
for the description of which see below.

Habitat.—The specimens of Ascorhynchus minutus were dredged in the neighbourhood
of Melbourne, at

Station 161. April 1, 1874. Off entrance to Port Philip. Depth, 38 fathoms. Sea
bottom, sand.

Observations.—This species seems to be nearly allied to Ascorhynchus ramipes, Bohm
(sp.). Yet it may be easily distinguished from it by the following characteristics :—

1. The total length of the body of Ascorhynchus ramipes is 11 mm., of the proboscis

REPORT ON THE PYCNOGONIDA. 57

3 mm., whereas the length of the body of Ascorhynchus minutus is.only 6°4 mm., and
that of the proboscis 2 mm.

2. The abdomen of Ascorhynchus ramipes is about as long as the proboscis, while
that of Ascorhynchus minutus is nearly one-third the length of the proboscis.

3. On the dorsal surface the thoracic segments and the lateral processes in Asco-
rhynchus ramipes show round knobs, in Ascorhynchus minutus distinct prickles.

4, The four last joints of the ovigerous legs of Ascorhynchus ramipes are furnished
with a single row of denticulated spines; those of Ascorhynchus minutus with three distinct
rows. (I think this difference is not a real one: Béhm’s observation and description will,
no doubt, in this respect, be found deficient.)

5. The first true leg of Ascorhynchus ramipes is not furnished with a claw, that
of Ascorhynchus minutus has a small, but distinct claw.

Ascorhynchus orthorhynchus, n. sp. (Pl. V. figs. 11-13; Pl. VI. figs. 1-4; Pl. XV.
figs. 14, 15).

Diagnosis.—Proboscis almost half the length of the body. Abdomen not quite one-
third the length of the proboscis. Dorsal surface with a row of prickles, also the lateral
processes.

Description.—
Length of the proboscis, . 4 . : : : 0 10 mm.
Length of the trunk, : ' ; ; ; abies ; 94 ,
Length of the abdomen, . ; : : F : : Sie Ss
Total length of the body, . 7 : . ; : 3 224 ,,
Length of the palpi, : . . : : . ; ee op
Length of the third leg, . : c : A , . BO)
Length of the ovigerous leg, - : : ’ : ; 20;

The body of this species is very slender and almost smooth. The proboscis does
not incline to the ventral side, and is not so much swollen as in the other species of
Ascorhynchus, consequently the form is not pyriform, but rather club-shaped. The
proboscis shows longitudinal furrows; the mouth is, as in the other species, triangular
and very small (Pl. XV. fig. 14).

The cephalothoracic segment is comparatively short, being only half as long as the
proboscis ; the mandibles and the palpi are placed on, distinct prominences. The
oculiferous tubercle is elevated and conical, and furnished with four distinct eyes; the
lateral processes for the ovigerous legs are very small, those for the first pair of true legs as
well as those for the following legs are of considerable size. The lateral processes of the true
legs are widely separated, thus contributing to the slender appearance of the whole body,
Posteriorly the cephalothoracic, as well as the two following segments, are consider-
ably elevated dorsally, while the anterior part of the following segment is much narrower,

(ZOOL, CHALL, EXP,—PART x,—1881,) K 8

58 THE VOYAGE OF H.M.S. CHALLENGER.

and placed lower; these three elevations bear in their centre strong conical prickles
(Pl. V. fig. 11). Similar prickles, though a little smaller, are also to be observed dorsally
on the lateral processes close to the margin of the articulation with the leg.

The mandibles of the female specimen (the only one procured) are small, but
distinctly three-jointed. The first two joints are extremely slender and of equal length ;
the third joint (Pl. VI. fig. 1) is very small, and furnished with rudiments of claws
only.

The palpi are very slender, and ten-jointed. The first joint is small, the second—
correctly observed by Béhm in Ascorhynchus ramipes—much smaller still, the third the
longest of all, the fourth small, the fifth not quite half as long as the third, the sixth
about the same length as the fourth, and the seventh twice as long as the sixth; the
three last joints decrease regularly in length. ‘The first four joints are nearly smooth,
distinct hairs are observed towards the extremity of the fifth jomt, and on the five
following joints (Pl. V. fig. 13). These hairs exhibit the curious form observed by
Bohm in the hairs of the palpi of Ascorhynchus ramipes; they are also found in
Ascorhynchus minutus (Pl. VI. fig. 16).

The first three joints of the ovigerous legs are small, the fourth is the longest ;
the fifth and sixth, which are a great deal smaller, and the seventh, which is extremely
small, are quite straight. The last three joints are placed at right angles to the fore-
going. All the joints are almost entirely smooth, with the exception of a few hairs
towards their extremities. The claw is very small. The denticulated spines on the
four last joints are placed in three or four rows; their form can be understood from the
drawing in fig. 3 of Plate VI.

The legs are more than twice as long as the body; the second joint is twice
as long as the first, the third is as long as the first. The fourth joint is considerably
swollen, the fifth nearly as long but a great deal narrower than the fourth, the sixth
much narrower and a little longer also. Of the two tarsal joints the second is longer
than the first and considerably curved, and the claw is nearly half as long as the second
tarsal joint. The hairs on the legs are very small, and can only be seen with the micro-
scope. Some stronger hairs are placed at the distal ends of the joints.

The single specimen brought up by the dredge is a female (having the fourth joint of
the legs swollen and the ovigerous legs feeble). The genital pores are not very small, and
are found ventrally at the end of the second joint of every leg (PI. XV. fig. 15).
Judging from the whole exterior of the animal, it is a full-grown, or nearly full-crown,
specimen.

Habitat.—The only specimen of this species: was dredged north of New Guinea, at
Station 219. March 10, 1875. Lat. 1° 50’ S., long. 146° 42’ E. Depth of the sea,
150 fathoms. Sea bottom, mud.

Observations.—This curious form of Ascorhynchus does not show any remarkable

REPORT ON THE PYCNOGONIDA. 59

affinity with any of the other forms of Ascorhynchus described. Judging from the shape
of the proboscis, it comes nearest to some of the species of Colossendeis. Yet in that
genus the mandibles in the full-grown animal have totally disappeared, whereas Ascor-
hynchus orthorhynchus in all probability has these appendages in the adult state. I
do not believe, however, as I have said before, that this difference is in reality very
important, especially since I have observed among the specimens of Colossendeis gracilis
one furnished with long three-jointed mandibles, while these appendages were totally
wanting in the other specimens of the same species.

Oorhynchus, n. gen.

Diagnosis.—Proboscis ovate, inserted ventrally on the cephalothorax at a con-
siderable distance from the front margin. Mandibles rudimentary; palpi nine-jointed.
Ovigerous legs ten-jointed, the four last joints not furnished with one or more rows of
denticulate spines.

Oorhynchus aucklandie, n. sp. (Pl. VIL. figs. 1-7).

Diagnosis —Oculiferous tubercle horizontally directed forwards. Mandibles repre-
sented by single-jointed club-shaped bodies. First tarsal jomt of the legs extremely small,
auxiliary claws wanting. Abdomen very long, once and a half as long as the proboscis.

Description.—
Length of the proboscis, ; . : ¢ : , j 1 mm.
Length of the cephalothorax, j : C ; : ? OA) a
Length of the trunk, ; : : 3 c 5 3 ES cn
Length of the abdomen, : é : : : . c 1195) rp
Total length of the body, . : 5 : ; 6 ‘ 4:2 ,,
Length of the leg, . : : ; . : : 2 5°5 ,,

This very curiously-shaped Pycnogonid has the cephalothoracic segment short but
very broad, furnished at the front with a long cylindrical oculiferous tubercle which
projects horizontally beyond the extremity of the proboscis. The oculiferous, tubercle i is
furnished with four eyes, two placed dorsally, and two ventrally; the latter two are
the smaller. The cephalothorax is armed at the two corners with curiously-shaped spines
also projecting forwards, and above the attachment of the first pair of legs bears a couple
of long hairs placed on small knobs. Similar pairs of hairs or thin spines are also
observed on the two following thoracic segments on the dorsal surface between the lateral
processes for the insertion of the legs. The rest of the surface of the body is entirely
smooth. ‘The three thoracic segments are small, and the lateral processes are separated
by small intervals. The abdomen, on the contrary, is very long, being once and a half
as long asthe proboscis. The abdomen shows on both sides a row of poipaaeale long
and projecting hairs.

60 THE VOYAGE OF H.M.S. CHALLENGER.

The proboscis is inserted ventrally on the cephalothorax, at a considerable distance
from the front margin; it is of a distinctly ovate form, and bears the small triangular
mouth surrounded by slightly swollen lips.

The mandibles are represented by one-jointed robust club-shaped bodies, placed at
the front margin of the cephalothorax on both sides of the oculiferous tubercle, but not
reaching quite so far as that organ. The mandibles are covered all round with strong
hairs, placed at right angles to the surface, and when the mandibles are viewed from
below and anteriorly, the round cicatrice is observed where in all probability, at an earlier
date, a second joint has been inserted.

The palpi are nine-jointed and placed close to and on both sides of the base of the
proboscis. The first joint is very short, the second is the longest of all and directed
forwards, the third again is short, the fourth almost as long as the second, and bent so as
to form an angle with the first three jomts. The fifth joint is again very short, the
four last joints are nearly of the same length ; the sixth, however, is the longest, and the
eighth the shortest. All the joints are furnished with very strong hairs, which are
longest on the third and fourth joints, and decrease in size though not in number
towards the extremity of the appendages.

The ovigerous legs are strongly curved. Of the first three joints, which are not
so very small as is the case in other genera, the second is the longest, being nearly
twice as long as the first. The fourth and fifth joints are nearly of the same length and
are the longest of all. The sixth is not quite half as long as either of the two foregoing
joints; of the seventh to the tenth the first is the longest, the second much shorter
and the third a little shorter, while the last joint is extremely small and may easily
be overlooked. The first three joints are almost smooth, the two following are furnished
with very small hairs, and the sixth to the tenth with not very numerous but longer
hairs. The last joint but one is armed with one, the last with two not very strong,
comparatively broad, and slightly serrated spmes. The total length of the ovigerous
leg is not quite so long as that of the body without the abdomen.

The legs are comparatively strong and very hairy (Pl. VII. fig. 6). The lateral
processes are furnished with numerous small and curved spines; the first three joints of
the leg are small and nearly of the same length. The fourth joint is twice as long as the
third, and on the dorsal surface beyond the middle it bears a tubular process, directed
backwards towards the origin of the leg. The fifth and sixth joints are the longest in
the leg, and are nearly of the same length. The fifth joint, however, is a great deal more
slender than the fourth, and the sixth much more so than the fifth. The first tarsal joint
is extremely small, the second long and distinctly curved ; the claw is scythe-shaped,
and accessory claws are wanting. All the joints are furnished with long and strong
hairs, standing at right angles to the surface ; the last joints are covered with much more
delicate hairs.

REPORT ON THE PYCNOGONIDA, 61

The only specimen of this curious species dredged by the Challenger Expedition is
a male; the second joints of the two last legs bear on the ventral side distinct rounded

- tubercles, and at the tips of these knobs the small genital pores are to be observed.

Habitat— Oorhynchus aucklandie was dredged at Station 169. July 10, 1874,
Lat. 37° 34’ S., long. 179° 22’ B.. Depth, 700 fathoms. Temperature of the bottom,
42°C. Sea bottom, grey ooze.

No other species of Pycnogonid was dredged at this station.

Observations.—No doubt the genus Oorhynchus is nearly allied to other genera of the
same group, and especially to the genus Achelia. Although the shape of the body is
widely different, we find in this genus likewise rudimentary mandibles, ovigerous legs
furnished with rudimentary denticulated spines and with ‘the four last joints, in general,
almost of the same shape as those of Oorhynchus. In both genera the genital pores of
the males are placed on tubercles situated ventrally on the second joints of the two
posterior legs, They are distinguishable by the shape of the body, which is much

_ more concentrated and rounded in Achelia, by the number of joints in the palpi, and

by the absence of auxiliary claws from the legs of Oorhynchus, whereas all the species of
Achelia, as far as is known at least, are furnished with them.

Colossendeis, Jarzyusky.

Colossendeis gigas, n. sp. (Pl. VIII. figs. 1,2; Pl. X. figs. 1-5).

Diagnosis.—Proboscis bottle-shaped ; cephalic part of the cephalothoracic seoment
triangular and distinct; eyes obsolete ; third joint of the palpus longer than the fifth,
palpus as long as the body ; claws of the legs minute.

Description.—

No. 1. No, 2. No. 3. No. 4.
Length of the proboscis, : . : 47°5 mm. 29 mm. 15 mm. 22 mm.
Length of the trunk (with the abdomen), F 32°'D ,, 20°5,, 1 Des US. 655
Length of the abdomen, : : : 6 45 3°5,, 2; Dilys
Length of the palpus, A ; 5 81 3 5S. 55 4 38°5 ,,
Length of the ovigerous leg, . : E 137 " 90) |; 49 ,, OO
Length of the leg of the third pair, . : 301 5 PAU 1s 143 ,,

The body of this gigantic Pycnogonid is robust; nevertheless there are distinct
intervals between the lateral processes. In the large specimen (No. 1) the surface of the
body is quite smooth ; the palpi alone are furnished with strong hairs, and the ovigerous
legs with small ones, while the extremely small hairs on the legs can only be seen with °
alens. In the younger specimens the hairs are by no means so scarce. Those on the
trunk, the proboscis, and the lateral processes are still very small, but the hairs on the
legs are much more distinct, and, especially at the distal extremities of the joints of the
legs, rows of short strong hairs may be observed ; finally, the palpi and the ovigerous legs

62 THE VOYAGE OF H.M.S. CHALLENGER.

show in these younger animals strong but not very long hairs projecting vertically from
the surface.

The proboscis is bottle-shaped and very long. The lower stalk-like and more slender
part (the neck of the bottle) can easily be distinguished from the middle part which is
considerably swollen, whereas the anterior part is a little narrower again, but by no means
so narrow as the stalk-like part. The mouth is triangular and very large. The cephalic
part of the cephalothorax in this species is sharply divided from the thoracic part, the
latter forming a true first thoracic segment. The cephalic part has, when viewed dorsally,
a triangular shape ; it bears almost exactly in the middle a very blunt oculiferous tubercle.
In the younger specimens this tubercle is conical, much more elevated and pointed at the
extremity ; it shows neither pigment nor lenses.

The four thoracic segments are closely united, so that their terminations are not
visible; the origin of the lateral processes for the insertion of the legs is, on the contrary,
distinctly marked by a line.

The abdomen is club-shaped and not longer than ‘5th of the total length of the
body. As in the other species of the genus Colossendeis it is connected with the thorax
by means of an articulation.

The palpi are as long as, or a little longer than, the body. The two first joints are
extremely small, the third is very long, the longest of all the joints of the palpi;
it is a little swollen at its beginning and again at the extremity. The fourth joint is
again very small, the fifth almost as long as the third; the sixth is again much
shorter, nearly one-fourth the length of the fifth. Of the last four joints the seventh
is the longest, the eighth being only half its length, and the ninth and tenth,

which are of equal length, being still shorter than the eighth. The first four joints
are almost quite smooth, while the following joints are furnished with short but rather
strong hairs.

The ovigerous legs, as in the other species of this genus, are attached close to the
base of the palpi. The lateral processes for the ovigerous legs are found at the ventral side,
immediately behind and close to the first jomt of the palpi. The first three joints of
the ovigerous legs are extremely short, not longer than they are broad. The fourth
joint is very long (almost as long as the proboscis) and not inconsiderably swollen
at the extremity. The fifth joimt is again short, and this jot serves—as was
observed by Wood-Mason —to elbow the ovigerous leg. The sixth is still longer than
the fourth and exactly as long as the proboscis. The last four joints gradually become
more slender; they are nearly equal in length and very short, the length, however,
decreases a little from the seventh to the tenth joint. At its extremity the last
joint bears a very small hook-like curved claw, the imner surface of which is quite
smooth.

1 Wood-Mason, On Rhopalorhynchus kroyeri, Journ. of the Asiatic Soc. of Bengal, Calcutta, vol. ii., 1873.

REPORT ON THE PYCNOGONIDA. 63

The last four joints describe a spiral curve; so that the tenth lies parallel to the seventh.
Their inner surfaces are furnished with numerous rows of very flat spines. In the oldest
specimen there are about twelve rows, making the total number of spines for every joint
several hundreds. None of these spines, however, show the original shape ; they are all of
them broken by use or by age, and those placed towards one side especially are very short
and rudimentary. On the other side they grow longer (Pl. X. fig. 2), and, covered
by this outermost row of longest spines, some short thimble-shaped knobs (fig. 5) are to
be observed. Such is at least the condition of the flattened spines on the last four joints of
the ovigerous legs of the gigantic male dredged at Station 146. The specimen second
in size is a great deal smaller and in all probability is not quite adult. Here the
spines, placed in about eight rows, show a much more regular shape (fig. 8); their
margins are furnished anteriorly with very small hairs. These hairs are rather
firm, are not at all injured by the action of alcohol, and must not, I believe, be con-
sidered as cilia. The spines are in the middle a great deal narrower, and broader again
at the extremity, the broader part has the shape of a rhomb. In the earliest stage the
spines are much smaller and beautifully spatulate. The small hairs extend here to beyond
the middle (Pl. X. fig. 4).

This species has exceedingly iene legs. The first three joints are very small, the
three following very long; the fourth is the longest, the fifth a Jittle shorter, the sixth
again a little shorter; the two last joints are small again ; the second tarsal is only half
as long as the first. The claw measures about one-third the length of the second tarsal
jomt; there are no auxiliary claws. The joints of the leg, from the fourth to the
eighth, gradually decrease in thickness. The hairs, which on the legs of the large adult
specimen are extremely small and oo are stronger and more numerous on the legs of

_ the younger specimens.

In regard to the sexes of the specimens of this species dredged during the voyage of
the Challenger, Iam sure only of the gigantic specimen. This is a male ; it shows genital
openings on the ventral surface not very close to the distal margin of the second joint of
the two posterior pairs of legs. About the other specimens, whose genital openings I failed
to observe, I am in doubt whether they are young males or females. The colour of the
specimens is light yellow, nearly the same as that of all other Pycnogonids preserved in
spirits. The large full-grown male, however, is of a much darker orange-red colour, with
beautiful red bands over the proboscis, at the extremity of the joints of the legs, &e.

Habitat.—Colossendeis gigas, seems to occur in different parts of the southern
ocean; it was dredged at

Station 146. December 29, 1873. Lat. 46° 46’S., long. 45° 31’ E. Depth of the
sea, 1375 fathoms. Temperature of the bottom, 15° C. Sea bottom, globigerina

00ze.
Station 147. December 30, 1873. Lat. 46° 16’ 8, long. 48° 27’ E. Depth of the

64 THE VOYAGE OF H.M.S. CHALLENGER,

sea, 1600 fathoms. Temperature of the bottom, 0°8° C. Sea bottom, globigerina
00ze.

Station 300. December 17, 1875. Lat. 33° 42’ §., long. 78° 13’ W. Depth 1375
fathoms. Bottom temperature, 1'5° C. Sea bottom, globigerina ooze.

Of all the species of this genus known at present, this species of Colossendeis shows
by far the greatest affinity with Colossendeis leptorhynchus, which I shall describe further
on. ‘The latter species, however, is much more slender.

Colossendeis leptorhynchus, n. sp. (Pl. VIII. figs. 3-7).

Diagnosis.—Proboscis almost cylindrical. Cephalic part of the cephalothoracic seg-
ment distinctly separated from the thoracic part ; eyes obsolete ; third joint of the palpus
shorter than the fifth; palpus much longer than the body. Legs and _ proboscis
extremely slender. Claws of the legs minute.

Description.—

Male Female
Length of the proboscis, . - : . = 28mm. 33 mm.
Length of the trunk with the Bpanren, : : ; : US cs 1: es
Length of the abdomen, . ; 5 - ; - 2:25, 2593,
Length of the palpus, . . » - . ; SD Gasih? Wolhew tes
Length of the ovigerous legs, . eens 0 : 56) 5; SVG Ne
Length of the leg of the third pair, : : : < HAS) ee pLOG. ys

The body, and especially the proboscis and legs, are a great deal more slender than
in Colossendeis gigas. The intervals between the lateral processes are not quite so wide
as the thickness of these processes, The surface of the body is quite smooth, but the
palpi and ovigerous legs, and the last five joints of the legs, are furnished with extremely
small hairs.

The proboscis is extremely long, more than twice as long as the trunk; about the
middle it is slightly swollen. The cephalic part of the cephalothorax is distinctly
separated from the thoracic part. It is elongated, a little more slender towards the end,
and bears on the dorsal surface, about the middle, a small blunt knob as a rudimentary
oculiferous tubercle.

The four thoracic segments are closely united. The abdomen is small, about 1-18th
of the total length of the body. The palpi are not very loug. ‘The first two and the
fourth joints are extremely small ; the third is long, and the fifth a great deal longer still.
The sixth joint is shorter than the seventh, and of the last three joints (fig. 5), the third
is by far the longest. The relative lengths of the joints of the ovigerous legs is the
same as in Colossendeis gigas, Hoek ; the sixth joint is again considerably longer than
the fourth, and the fifth is extremely short. The last four joints decrease in length, and
the claw is very small (fig. 6).

The first three joints of the legs are very small, nearly as long as broad ; the following

REPORT ON THE PYCNOGONIDA. 65

three are very long and slender, and not inconsiderably curved. Their relative length
is the same as in Colossendeis gigas. Of the last two joints, the first is longer than the
second. The claw is small.

Of this species seven adult and two young specimens were dredged during the
cruise of H.M.S. Challenger. By stretching out the legs parallel with each other, the
body of the animal assumes a very peculiar aspect.!. Of the eight adult specimens,
seven are females—one only a male. Both the females and the male have genital
openings only on the two hindermost legs, where they are placed on the ventral surface
of the second joint of the leg. Perhaps the ovigerous legs of this species, and in that
case probably of the other species of this genus also, have lost their ege-bearing function.
Small capsules filled with numerous eggs were attached to several joints of the legs,
but as these eggs were quite undeveloped, it was impossible to determine whether they
belong really to this animal, or to some other inhabitant of the same locality. The
capsules, I observed, were attached to the fourth joint of the leg in a female, and to the
second joint of the leg in the single male specimen.

Habitat.—This species was dredged at the same stations as the foregoing species
(Colossendeis gigas), and also at a fourth station (310).

Station 146. December 29, 1873. Lat. 46° 46’ S., long. 45° 31’ E. Depth of the
sea, 1375 fathoms. Temperature of the bottom, 1°5° C. Sea bottom, globigerina ooze.

Station 147. December 30, 1873: Lat. 46° 16’S., long. 48° 27’ E. . Depth of the
sea, 1600 fathoms. Temperature of the bottom, 0°8° C. Sea bottom, globigerina ooze.

Station 300. December 17, 1875. Lat. 33° 42’ §., long. 78° 13’ W. Depth of the
sea, 1375 fathoms. Temperature of the bottom, 1°5° C. Sea bottom, globigerina
ooze.

Station 310. January 10, 1876. Lat. 51° 30’S., long. 74° 3’ W. Depth of the
sea, 400 fathoms. Temperature of the bottom, 7°9° C. Sea bottom, mud.

Observations.—This species is distinguished from the foregoing by its much more
slender form and shorter palpus. From Colossendeis angusta, G. O. Sars (Arch. f.
Math. og Naturvid., vol. ii. p. 268, 1877), and other species, it may be easily distinguished
by the dimensions of the joints of the palpus; for, as far as I know, Colossendeis
leptorhynchus is the only species of this genus which has the fifth joint of the palpus
considerably longer than the third. The form of the cephalic part of the cephalothorax,
and the extremely small claws at the ends of the legs indicate, I believe, a near relation-
ship between this species and Colossendeis gigas.

Colossendeis gigas-leptorhynchus. -
A single specimen—unfortunately defective—dredged at Station 158, shows to a

1 This, of course, refers to the animal preserved in spirits. I observed the-same thing in living specimens of N’ ymphon
gracile, Leach, and Pallene lrevirostris, Johnston.
(ZOOL. CHALL, EXP.—PART x.—1881.) : K9

66 THE VOYAGE OF H.M.S. CHALLENGER.

certain extent the characteristics of Colossendeis gigas, and in other respects those of
Colossendeis leptorhynchus. I therefore wish to consider it as an intermediate form. Its
dimensions are as follow :—

Length of the proboscis, . : : : : : 26 mm.
Length of the trunk with the ahaa, : F : < : 18>;
Length of the palpus, i : ; A - 4 334 ,,
Length of the ovigerous leg, : 5 ; : : q
Length of the leg, . 5 ; 2 F 5 ; c 37 +,,

As I consider that this specimen is not quite adult, I will not give a detailed de-
scription of it. I only wish to point out that the form of the proboscis, though a little
more slender, quite agrees with that of Colossendeis gigas, whereas the relative length
of the joints of the palpus, and that of the whole palpus, isthe same as in Colossendeis
leptorhynchus, viz., the third joint of the palpus is 8°5 mm., and the fifth 14mm. The
total length of the palpus is only three-quarters the length of the body.

The specimen is a young female, with the body almost smooth, and with legs only
furnished with extremely small hairs.

Habitat.—This curious form was dredged at Station 158, March 7, 1874. Lat.
50° 1’ §., long. 123° 4°E. Depth of the sea, 1800 fathoms. Bottom temperature,
03° C. Sea bottom, globigerina ooze.

Colossendeis robusta, nu. sp. (Pl. IX. figs. 4, 5).

Diagnosis.—Proboscis club-shaped, shorter than the trunk. Body and legs rather
stout, with large intervals between the lateral processes for the insertion of the legs.
Palpi not very long, a great deal shorter than the body, with the third joint longer than
the fifth. Legs not very slender, furnished with a claw, which is almost half as long as
the second tarsal joint. Oculiferous tubercle conical, with four eyes.

Description.—
Length of the proboscis, . : : : - : 15 mm.
Length of the trunk with the seen: : : . : : ile} Be
Length of the abdomen, : ~ : : é é : 3°5,,
Length of the palpus, : : 3 : 3 ; : PAI,
Length of the ovigerous legs, " . - : . 6 BPI op
Length of the leg of the third pair, < é = : ae 113";

Only a single specimen of this beautiful and robust form was dredged. All the
segments of the body are closely united, the cephalic part is comparatively short, and
bears a conical, robust, not much elevated, oculiferous tubercle. This tubercle shows four
distinct eyes, two of which are large and directed forwards, while the two small ones are
directed backwards. :

REPORT ON THE PYCNOGONIDA. 67

The intervals between the well-developed lateral processes are comparatively large.
The proboscis is not quite half so long as the total length of the body. It is very stout,
and shows a considerable swelling in the middle, and another at the extremity. The
abdomen is small, its length about one-fifth the length of the trunk.

The palpi are comparatively stout, shorter than those of Cblossendeis gigas, but
longer than those of Colossendeis leptorhynchus. The first two joints are very small,
the third is by far the longest of all the joints. The fourth is short again, the
fifth only three-fourths as long as the third, the sixth to the tenth are nearly of
the same length, the seventh, however, is a little longer. The joints are almost per-
fectly smooth, with the exception of some very small hairs visible only with the
microscope.

The ovigerous legs have the first three joints short, the fourth and sixth of about the
same length, and comparatively long. The fifth (the elbow-joint) is short. The four
last joints are almost of the same length, becoming more slender from the first to the
fourth. The claw is small and smooth; the place of the denticulate spines of the
four last joints is filled up by short strong knobs of a conical or rounded shapé. They
are placed on excavations of the chitinous skin, and with the exception of the two rows
on one side, are placed rather irregularly.

The legs are not very long. Those of the third pair are the longest. The first and
the fourth leg of the right side are, in the Challenger specimen, quite rudimentary. In
the full-grown leg the fourth and the sixth joint have the same length, whereas the fifth
is a little shorter. Of the two tarsal joints the first is longer than the second. The claw
is robust, about half as long as the second tarsal joint.

The only specimen brought home by the Challenger Expedition is a female. Its
genital openings are not very large, and are found ventrally on the second joint of all
the legs.

The animal is entirely smooth, and of a beautiful orange colour.

Habitat.—This species was dredged off Christmas Harbour, Kerguelen, 29th June
1874. Depth of the sea, 120 fathoms.

Observations.—This species cannot easily be confounded with any of the other
species; it is distinguished by being stout, yet comparatively slender, by the form
of the proboscis, and the presence of four distinct eyes. It is rather a shallow-water

species.

Colossendeis megalonyz, n. sp. (Pl. IX. figs. 1-8).

Diagnosis.—Proboscis club-shaped, somewhat bent over to the ventral side. Cephalic
part of the cephalothorax not distinctly separated. Oculiferous tubercle conical, with
four eyes. Third joint of the palpus longer than fifth. Body and pie slender. Claws
of the legs as long as the second tarsal joint.

68 THE VOYAGE OF H.M.S. CHALLENGER,

Description.—

Length of the proboscis, . E ; 20 mm. 8 mm. 13:5 mm. 17°5 mm.
Length of the trunk, ; : j 10:5). 8. i ee 10D.
Length of the abdomen, . 5 . 2°5 5, Dixs Ns Ye ie ee
Total length of the body, . : : Domes,

Length of the palpus, : ; ‘ 26° 55

Length of the ovigerous leg, : - SOEs.

Length of the leg of the third pair, : Qi

The proboscis of this species is club-shaped, a little bent over to the ventral side ;
longer than the trunk with the abdomen. The cephalothoracic segment is comparatively
small, and not distinctly divided into a cephalic and a thoracic part. Between the
lateral processes of the thoracic joints large intervals are to be observed. The oculi-
ferous tubercle is large and high, conical, furnished with four eyes. Of these, two are
very large and directed forwards, while the two directed backwards are a great deal
smaller and in all probability are rudimentary. The abdomen is small, only 1-13th
of the total length of the body.

The palpi are slender, and the lengths of their joints are not very characteristic.
The third joint is much longer than the fifth, and of the three last joints the eighth is
very small, the ninth and tenth considerably longer. In the ovigerous legs the fourth
and sixth joints have nearly the same length, while the fifth is not quite half as long.
The four last joints are small, and nearly equal in length, growing however a little
shorter and more slender towards the tenth joint. The claw is very short.

The distribution and form of the denticulate spines is in this species very charac-
teristic. There are two rows of comparatively long and flat spines, the margins of which
show when greatly magnified very minute hairs; in addition to these two rows a
moderate number of smaller flattened spies are found scattered over that side of the
four last jomts which is bent inwards. I have figured these two rows and the irreeu-
larly placed spines in figure 3 on Plate IX.

The legs are not very long, nearly three times as long as the body in the
adult specimen, while the younger specimens have them much shorter. The
three first joints are: very short, the fourth is the longest, viz., 23 mm.; in a leg, the
fifth jomt of which measures 21 mm., the sixth is 18 mm. The two tarsal joints
are together as long as the sixth joint. The claw is large, almost as long as the second
tarsal joint.

The surface of the body and of the legs is almost entirely smooth. The palpi
show only very small hairs, and on the ovigerous legs hardly any hairs are to be
observed.

Of this species seven specimens were dredged. They are, I think, all young ones
with the exception of one specimen which is a male. It shows genital pores ventrally
on the second joint. of all the legs.

REPORT ON THE PYCNOGONIDA, 69

Habitat.—This specimen was dredged at the following stations :—

Station 149. January 29, 1874. Off Christmas Harbour, Kerguelen. Depth of
the sea, 120 fathoms.

Station 313. January 20, 1876. Lat. 52° 20’ S., long. 68° 0’ W. Depth of the
sea, 55 fathoms. Temperature of the bottom, 8°8° C. Bottom of the sea, sand.

Station 814, January 21, 1876. Lat. 51° 36’ S., long. 65° 40’ W. Depth of the
sea, 70 fathoms. Temperature of the bottom, 7°8° C. Bottom of the sea, sand.

Observations.—This species resembles Oolossendeis proboscidea, Sab., sp. (Appendix to
the Supplement of Captain Parry’s Arctic Voyage, 1824, p. cexxvi.), in the form of the
proboscis. . That species, however, is a great deal stouter, and has a much larger
body with comparatively short legs. Moreover, the body of Colossendeis proboscidea
is rather disc-shaped, and by no means so slender as that of Colossendeis megalonya.
This species ranges from Kerguelen as far west as the east coast of Patagonia; the
three stations, however, at which it was found are nearly under the 50th parallel.

Colossendeis gracilis, n. sp. (Pl. IX. figs. 6-8 ; Pl. X. figs. 6, 7).

Diagnosis.—Body slender, with wide intervals between the lateral processes ; pro-
boscis about as long as the trunk; palpus once and a half as long as the proboscis, with
the third joint longer than the fifth, the eighth joint extremely small, and the ninth
joint laterally inserted on the front of the foregoing. Ovigerous legs about once. and
a half as long as the total length of the body. ‘The claw of the legs longer than the
second tarsal jot. Oculiferous tubercle conical, without eyes.

Description.—
Length of the proboscis, : : : a 5 6:5 mm, 5°8 mm.
Length of the trunk, : ; : ; : OL as, 52 5
Length of the abdomen, . 3 : ‘ : es oy 1 a ay
Total length of the body, : : 0 : etl FF Ve
Length of the palpus, ; : é : : LD 55 S)
Length of the ovigerous leg, . - : : » 22 3 NE)) op
Length of the leg of the third pair, . . . 5 Ol 6 40 ¥

The proboscis of this species is nearly as long as the trunk, and a little shorter than
the trunk with the abdomen. It is a little swollen nearly in the middle, but in some
specimens it is almost quite cylindrical. The cephalothoracic segment has the cephalic
part, which is rather triangular, in some degree distinct. It bears anteriorly the very
high conical oculiferous tubercle.

The lateral processes for the insertion.of the legs are wilely separated. The abdomen
is not very short, and in one of the specimens is a little more swollen at the extremity
than in the others.

Mandibles (Pl. X. fig. 6) are present in one of the specimens. It is a young male;

70 THE VOYAGE OF H.M.S. CHALLENGER.

the largest specimen, however, of this species dredged, These mandibles are very long
and slender, three-jointed, little shorter than the proboscis. The third joint terminates
in a pair of small and slender pincers.

Of the palpi the third joint is longer than the fifth. Of the last three joints the
first is extremely small and broad (Pl. IX. fig. 7), and the ninth is inserted, not into
the middle of the front part of that joint, but quite laterally. This ninth joint itself
is cylindrical, and more than twice as long as the foregoing, whereas the tenth is a little
more slender and still longer than the ninth joint.

The joints of the comparatively long ovigerous legs have characteristic proportions
in all the species of the genus Colossendeis. The claw at the end of the tenth joint
is very small. The denticulate spines on the last four joints are not numerous, the
number of rows not exceeding four. Of these two are very regular, with the spines
placed close to one another, but those of the two other rows are much more irregularly
scattered over the remaining part of the inner surface of the joint (Pl. IX. fig. 8 ;
Pl, A ig.7). A”

The lengths of the’ several legs of one and the same specimen only show slight
differences. The third leg is, in the three specimens I have examined, the longest, and
measures nearly three and a half times the length of the body. The claw is very long,.
still longer than the second tarsal joint. Genital pores are present on the second joint
of every leg. As to the sex of the three specimens dredged during the voyage of
H.M.S. Challenger, I have only been able to ascertain that the specimen with mandibles
is a male.

The body and legs are almost entirely smooth; small hairs are only to be observed
on the last joints of the palpi.

Habitat.—This species was dredged between the Cape of Good Hope and Kerguelen
Island.

Station 146. December 29, 1873. Lat. 46° 46’ S., long. 45° 31’ E. Depth of the
sea, 1375 fathoms. Temperature of the bottom, 1°5°C. Bottom of the sea, globigerina
ooze. ; f

Station 147. December 30, 1873. Lat. 46° 16’S., long. 48° 27’ E. Depth, 1600
fathoms. Bottom temperature, 0°8° C. Bottom of the sea, globigerina ooze.

Observations.—To this species Colossendeis media and Colossendeis brevipes, which
I shall describe further on, are closely allied. The occurrence of mandibles in one of
the specimens of this species is very interesting. Although larvee of any species of
Colossendeis have never been observed, they doubtless are furnished with three pairs of
cephalic appendages. Of these the adult animal has always lost the first pair; and
whenever, as in the case in question, this first pair is observed in the adult animal, it
must be considered as a case of atavism, showing that the loss of mandibles in the
adult animal has been’ comparatively recent.

REPORT ON THE PYCNOGONIDA. (ill

Colossendeis medic, n. sp. (Pl. X. figs. 10, 11).

a half the length of the proboscis ; ninth joint
not attached tara to the eighth; together they are as long as the tenth joint.
Denticulate spines of the four last joints of the ovigerous legs in five distinct rows.
Legs not quite three times as long as the body. Otherwise this species resembles the
foregoing.

Description.—
Length of the proboscis, . : 5 : : r , 74 mm.
Length of the trunk, ; : ; : : : 64
Length of the abdomen, . F ; : é : ; ee eA
Total length of the body, . : : i ; : ( 154,
Length of the palpus, 5 4 ; é . ; oo Ne
Length of the ovigerous leg, - ‘ . . 3 PAV) pp
Length of the leg of the third pair, : 3 : ; : 454 ,,

This species is nearly of the same shape and the several parts show almost the same
proportions as in Colossendeis gracilis, Hock. The only differences are the follow-
ing :—

1. The palpi are longer, and of the three last joints the very small eighth joint does
not bear the following joint laterally, but quite in front (Pl. X. fig. 10).

2. The denticulate spines of the ovigerous legs (of the four last joints) are placed in
five distinct rows. They are small with the exception of those-of the outermost row,
which are a great deal larger. These spines have the flattened shape of those of other
species of Colossendeis, Those which are not broken, show on the margin very small
hairs.

3. The legs are not quite thrice as long as the body. The fourth joint is twice as
long as the sixth. The claw is longer than the second tarsal joint. ‘The two tarsal joints
are about the same length, together they are as long as the body.

The body and legs are almost entirely smooth; when seen with the microscope very
short hairs are to be observed; those on the palpi are a little stronger. On the second
joint, on the ventral surface, of every leg very small genital pores are to be observed.
However, as the two specimens of this species probably are not quite adult, I could not
determine to which sex they belong.

Habitat.—This species was dredged at Station 298. November 17, 1875. Lat.
34° 7’S., long. 73° 56’W. Depth of the sea, 2225 fathoms. Bottom temperature, 1°3° C.
Bottom of the sea, grey mud. os,

Observations.—This species is nearly allied to Colossendeis gracilis. However, as the
differences I have pointed out are present equally in both specimens, I cannot consider
them identical with that species.

72 THE VOYAGE OF H.M.S. CHALLENGER.

Colossendeis brevipes, n. sp. (Pl. X. figs. 8, 9).

Diagnosis.—Lateral processes not very widely separated. Palpus less than once and
a half as long as the proboscis, with the three last joints bent over like a hook. Ovigerous
legs with the denticulate spines of the four last joints numerous and comparatively short
Length of the legs unequal, short. Otherwise this species resembles Colossendeis gracilis,
Hoek.

Description.—

Length of the proboscis, : 3 : : : 9 mm. 8-5 mm.
Length of the trunk, ; ; : - : UfPBS ee 1D 5
Length of the abdomen, 5 ‘ ; : : 2°5 ,, Dy ate
Total length of the body, ‘ : 3 5 . nt eee Itsy
Length of the palpus, : : : s ‘ Ze psy UNS)
Length of the ovigerous leg, . : ; : : 29a. 2D as
Length of the leg of the first pair, ; : : : DOM es By a
Length of the leg of the second pair, . : : : 620aF; Se
Length of the leg of the third pair, . Sie sak: ; D3) 55 C2
Length of the leg of the fourth pair, . : : 5 ADTs 52°5 ,,

This true deep-sea species is also nearly allied to Colossendeis gracilis. The first time I
examined it I was struck with the shortness of the legs, especially in the largest specimen;
but as it is possible that this length varies greatly under different circumstances—as it
certainly does with age—it is necessary to use the utmost care in judging of this charac-
teristic mark. The body, proboscis, trunk, and abdomen are as in Colossendeis gracilis,
the only difference being that the lateral processes are not quite so widely separated.

The palpus is short, only one-fourth as long as the proboscis. The last three joints
are extremely short, shorter than the seventh joint ; they are bent like a hook, the tenth
joint hanging down parallel with the seventh joint (fig. 8).

The ovigerous legs are comparatively long, 29 mm. in a specimen of 19 mm. The
last four joints are small and furnished with a rudimentary claw, the length of which is

-nearly one-fifth the length of the tenth joint. A drawing of the denticulate spines on
one of the four last joints of the ovigerous leg is given in fig. 9. The spines are short
and flat and do not show small hairs at the periphery. There are two regular rows, the
outermost of which has the stoutest and longest spines, whereas the irregularly placed
spines on the other side decrease in size. The length of the legs is very unequal. The
specimen with the shortest legs is a full-grown female. The claw at the end of the
eighth joint is very long, longer than that joint. The body and legs are almost entirely
smooth ; there are small hairs on the last joints of the palpi.

The genital pores of both specimens, the largest of which is a female, are found
ventrally on the second joint of all the legs.

Habitat.—This species was dredged from the greatest depth at which a Pyenogonid
has been found, viz., 2650 fathoms,

REPORT ON THE PYCNOGONIDA. 73

Station 325. March 2, 1876. Lat. 36° 44’ S., long. 46° 16’ W. Depth of the sea,
2650 fathoms. Bottom temperature, 70'4° C. Bottom of the sea, grey mud. :

Observations.—Whether I am right or not in considering the specimens collected at
Stations 146 and 147 (Colossendeis gracilis, Hoek), Station 298 (Colossendeis media,
Hoek), and Station 325 (Colossendeis brevipes), as three different species can only be ascer-
tained by examining a larger number of specimens than are at my disposal. I can only
point out here the great affinity of these different specimens. However, I may be per-
mitted to state here, that whenever I speak of a specimen as adult, the statement is
based on the microscopical examination of transverse sections of the fourth joint of one
of the legs.

Colossendeis minuta, n. sp. (Pl. X. figs. 12-14).

Diagnosis.—Proboscis cylindrical, once and a half the length of the trunk with
the abdomen. Lateral processes not widely separated. Palpus once and a half as
long as the proboscis, with the last three joints of about the same length. Legs
extremely slender, about four and a half times the length of the body. Claw of the leg
half as long as the second tarsal joint.

Description.—
Length of the proboscis, . C . . - . é 4'8 mm.
Length of the trunk, ; ; ; : F : ; Deli vrese
Length of the abdomen, . 5 P ‘ 3 ; ; O:5aa
Total length of the body, . : c 5 : . é Sian;
Length of the palpus, ; : : : : : c 193) 5.
Length of the ovigerous leg, : : : : 4 : eS ey
Length of the leg of the third pair, : : c : ; 35

Only a single specimen of this species was dredged. It is a small animal with a
comparatively long proboscis and very slender legs. The body is not extremely slender,
there being only small intervals between the lateral processes for the insertion of the
legs. The cephalothoracic segment is small and not distinctly divided into a cephalic
and a thoracic part. Quite near the front it is furnished with a blunt oculiferous
tubercle without eyes.

The proboscis is nearly cylindrical, it is a little swollen in the middle, and the mouth
is small and triangular. The abdomen is small; it is connected with the last thoracic
joint by a true articulation.

The palpus is slender, but not extremely long, being only once and a fourth as long as
the proboscis. The third joint is only a little longer than the fifth. Ihave given a
drawing of joints six to ten in fig. 13. The last three joints together are longer than the
seventh ; they are of about the same length, and comparatively slender. Beginning
with the fifth, all the joints are furnished with short but strong hairs, which have the
same shape as those on the legs and ovigerous legs.

(z0OL. CHALL, EXP,—PART x.—1881.) K 10

74 THE VOYAGE OF H.M.S. CHALLENGER.

The ovigerous legs are of the ordinary form. Only the middle of that part of the
surface of the four last joints which is turned inwards, is furnished with denticulate spines.
Their form is very peculiar, being flattened and much broader towards the extremity
(Pl. X. fig. 14). They are not very numerous and are placed in three rows only,
while every row contains about six of them. The margin of the spines is smooth.
The claw of the ovigerous leg is small, and the length of the several joints is as in the
other species of the same genus.

The legs are extremely long and slender. ~ With the exception of some small but
strong hairs, like those of the palpus, they are smooth. The first three joints are small ;
of the three following the first two (the fourth and fifth) are nearly of the same length,
whereas the sixth is considerably shorter, but much longer than the last two joints
together. Of these the first (the first tarsal joint) is about once and a half as long as the
second. The claws at the ends of the legs are about half as long as the second tarsal joint.

About the sex of the only specimen collected I am unable to form an opinion.
Perhaps it is not yet quite adult: extremely small genital pores are to be observed
ventrally on the second joint of every leg.

Habitat.—This interesting little Colossendeis was dredged by the Challenger at

Station 50. May 21, 1873. Lat. 42° 8’ N., long. 63° 39’ W. Depth of the sea,
1250 fathoms. Temperature of the bottom, 2°8° C. Bottom of the sea, grey ooze.

Observations.—This curious form is intermediate, I believe, between the short-nailed
Colossendeis leptorhynchus, with its extremely long proboscis, and the long-nailed Colos-
sendeis gracilis, with the comparatively short proboscis. The difference in length between
the third and the fifth joint,—in Colossendeis leptorhynchus the fifth joint is the longest,
and in Colossendeis gracilis it is the third joint which has the advantage—has almost dis-
appeared in Colossendeis minuta.

The species was dredged about two degrees south of Halifax ; though the Pycnogonids
of the neighbourhood of the coast of New England are comparatively well known, the
occurrence of a species of Colossendeis in those regions has not been recorded as yet.
And this, no doubt, is due to the circumstance that the species in question inhabits deep
water, while hitherto only the shallow water inhabitants have been carefully investi-
gated.

Discoarachne, n. gen.

Diagnosis.—Proboscis stout, cylindrical, tapering towards the extremity. Mandibles
wanting. Palpi five-jointed. Ovigerous legs not furnished with denticulate spines, ten-
jointed.

Discoarachne brevipes, n. sp. (Pl. VII. figs. 8-12).
Diagnosis.—Body disciform, consisting of the true body without any segmentation

REPORT ON THE PYCNOGONIDA. 75

and the closely united lateral processes. Legs short with auxiliary claws. Body and
legs smooth, furnished only with very small hairs.

Description.—
Length of the proboscis, . : ' : : . 0 21 mm.
Length of the abdomen, : z F ‘ : A li,
Total length of the body, . : é 4 : : ¢ 41 ,,
Length of the palpi, : : : ¢ : ° : 1k,
Length of the ovigerous legs, : : ; ; c : 25
Length of the legs, . 4 , ji . " : 5 (aes

The cephalothoracic joint is closely connected with the three other thoracic joints ;
the lateral processes are short and somewhat triangular, forming in connection with the
body a disciform surface, from which the legs radiate in different directions. The
proboscis is comparatively large, the form cylindrical, tapering towards the extremity.
The oculiferous tubercle, which is small, not very elevated, and furnished with four distinct
eyes, is placed dorsally on the middle of that part of the body, which corresponds with
the cephalothoracic segment.

The palpi are small, measuring about two-thirds the length of the proboscis. The
first and second joints are very short, the third joint is the longest of all, the fourth again
small, the fifth more than twice as long as the fourth, and comparatively slender. The first
two joints are smooth, the third joint is furnished up to the outer margin with three long
spines, and on its inside with three smaller spines, which are curved; the ventrally
directed surface of the same joint, which contains a large gland, hereafter to be described,
has, near the middle, four extremely small spines. The fourth joint is nearly smooth, the
fifth is armed with very large and numerous spines near the extremity.

The first joint of the ovigerous legs is very small, the second and the third are a little
longer, the fourth and the fifth are the longest, the sixth is short again, the seventh,
eighth, ninth, and tenth are about the same length, and gradually diminish slightly in
breadth. The first five joints are nearly smooth, towards the distal extremity the sixth
shows some short and not very strong spines, whereas the four following joints are
furnished in the same place with much stronger and slightly curved spines. Towards
the end of the tenth joint there are a considerable number of these spines, while a claw
and true denticulate spines are totally wanting.

The first three joints of the legs are small; of the three following, the middle joint is
the longest. The first tarsal joint is extremely short, the second comparatively long, and
very slender in comparison with the other joints of the legs. The claw is about one-
third the length of the second tarsal joint. The auxiliary claws are comparatively
long, two-thirds the length of the claw. The hairs on the different joints of the legs are
small; the distal extremity of these joints is, as a rule, furnished with a row of longer .
and stronger spines, especially at the end of the sixth joint. The first tarsal joint has

76 THE VOYAGE OF H.M.S. CHALLENGER.

numerous small hairs on the inner margin; the second is armed with three very strong
and broad spines on the inner margin near the base, while longer and much more
slender spines are present on the outer margin.

A single specimen of this species was collected during the cruise of H.M.S. Challenger.
It is a female with eggs in all stages of ovarian development, enclosed in the fourth joint
of the leg. The genital pores could not distinctly observe, but no doubt they are placed
ventrally near the distal extremity of the second joint of the leg.

Habitat.—This species was found at Seapoint near Cape Town in November 1873.

Observations. —The genus Discoarachne is in all probability nearly allied to Enders,
Philippi. But as that genus is difficult to make out from the insufficient description
of Philippi, I propose a new genus for the species in question, because Philippi’s form
had eight-jointed palpi, whereas the Challenger form, which must be a full-grown animal,
has only five-jointed palpi. This species with its short legs and highly concentrated body,
is a true littoral form.

Pallene, Johnston.

Pallene australiensis, n. sp. (Pl. XI. figs. 1-7).

Diagnosis.—Body extremely slender. Cephalic part of the cephalothoracic segment
distinctly separated from the thoracic part by means of a true articulation. Proboscis
short, inserted ventrally. Ovigerous legs with true denticulate spines, and a long
denticulate claw. Legs without auxiliary claws.

Description.—

Length of the proboscis, . é : : : : : 15 mm.
Total length of the body, . : : c : ; : (aS mm 5
Length of the ovigerous legs, : . 2 : : 2 C =A
Length of the leg of the-third pair, : : : : : 28 5

The body is extremely slender ; the cephalic part of the cephalothoracic segment
(neck) is much swollen at the tip for the insertion of the mandibles. A true articula-
tion divides this cephalic part from the thoracic part. The rather short oculiferous tubercle
is situated about the front of the thoracic part.

The intervals between the lateral processes, at the extremities of which the legs are
found, are very large. The abdomen is rudimentary and directed a little upwards. The
surface of the body and of the lateral processes is smooth. The proboscis is short and
inserted rather ventrally. It is constricted beyond the middle, and is much wider at the
extremity, where the very small triangular mouth is observed.

The mandibles are short and robust. The first joint reaches almost as far as the end
of the proboscis, the second joint is considerably swollen, and terminates in a pair of
short pincers. These are furnished with a single very small tooth towards the ex-
tremity.

REPORT ON THE PYCNOGONIDA. a

The ovigerous legs are inserted ventrally close to the lateral process of the first pair
of legs. Of the first three joints, which are small, the third is the longest ; the fourth
is a great deal longer, and the fifth is the longest of all, in the males it has a
strong knob near the extremity ; the sixth joint is almost as long as the fourth. The
four last jomts show no great difference; from the seventh to the tenth they
gradually diminish in length and in breadth. The claw is as long as the tenth joint,
and on the inside is furnished with a row of small spines. The hairs on the joints
of the ovigerous legs are not very strong. I have figured the denticulated spines in
Pw ties 5:

The legs are verylong. The second joint is thrice as long as the first and as the third.
In the female it is considerably swollen towards the extremity, where the genital
opening is observed on the ventral surface. Of the three following joints the fourth
and the fifth are nearly of the same length, while the sixth is almost once and a half as
long. The first tarsal joint is extremely short, and the second about eight times as long.
The claw is half as long as the second tarsal joint. The joints of the leg are furnished
with extremely long and slender spines; two are placed at the distal extremity of the
first joint, two in the middle of the second joint, and two others towards the extremity
of that joint; a row of slightly shorter ones is observed on the dorsal surface towards
the extremity of the third joint ; the fourth, fifth, and sixth joints are also furnished with
some of these hairs placed at irregular distances from one another; towards the extremity
of these joints a certain number of these hairs is invariably observed. The first tarsal
joint (fig. 6) shows only a few very short spines, whereas the second tarsal joint
towards the side opposite to the claw is furnished with a complete row of very stout
spines. Most of these spines, like the greater part of those placed on the other joints,
are not quite smooth, but are furnished on one side with sharp short triangular hooks
not unlike the teeth of a saw.

Of the three specimens of this species, one is a female, and two are males. I believe
they are all full-grown animals. One of the males shows the remains of ege-packets adher-
ing to the ovigerous legs. The genital openings of the females are much larger than
those of the males. Both sexes have them placed ventrally on the second joint of all
- the legs.

Habitat.—This beautiful species was dredged in the neighbourhood of Melbourne.

Station 162. April 2, 1874. Off East Moncoeur Island, Bass Strait. Depth of the
sea, 38 to 40 fathoms. Bottom of the sea, sand.

Also between Melbourne and Sidney at Station 163. April 4,1874. Lat. 36° 56’S.,
long. 150° 30’ E. Trawled in 120 fathoms. Off Twofold Bay.

Observations.—Perhaps this species is nearly allied to Pallene chiragra, Milne-
Edwards, Histoire naturelle des Crustacés, tom. iii. p. 535. He gives the following descrip-
tion of this species :—“ Corps trés-gréle ; téte courte mais cylindrique. Second article

78 THE VOYAGE OF H.M.S. CHALLENGER.

des pates-mAchoires trds-renflé, et premier article du thorax extrémement allongé. Pates
environ cing fois aussi longues que le corps, sans crochets accessoires au bout. Pates
accessoires de la femelle de dix articles.” However, as in this description the very
distinct spines on the legs have not been mentioned, which, if present, would certainly
have been seen by Milne-Edwards, I think it probable that his Pallene chiragra is a
nearly allied but distinct species. Jarvis Bay, New Holland, where Milne-Edwards’s
species was collected, is not far from Station 163.

Pallene levis, n. sp. (Pl. XI. figs. 8-12).

Diagnosis.—Body robust, lateral processes scarcely separated. Body and legs smooth.
Proboscis short, conical ; inserted about the front of the cephalothoracic segment. Ovi-
gerous legs with denticulate spines and a long claw. Legs without auxiliary claws.

Description.—
Length of the proboscis, . 5 : : : é : 1 .mm.
Length of the trunk, ; : ‘ : : 3 2°66 ,,
Length of the abdomen, : : : . . DONG:
Total length of the body, . : 3 : 5 , , Cae
Length of the ovigerous leg, ; A : : ‘ - One a5
Length of the leg of the third pair, ‘ ¢ : : . PANS a ye re

The body of this species is robust. The cephalothoracic segment is of a curious
shape: it is considerably swollen at the front, where it bears the proboscis and the
mandibles ; it is constricted in the middle, thus forming a sort of short neck, and it is
much wider again at the back, where it bears dorsally the oculiferous tubercle, and
ventrally the short lateral processes for the insertion of the ovigerous legs. The
oculiferous tubercle, with two larger eyes directed forwards and two smaller ones back-
wards, is situated almost exactly above the insertion of the ovigerous legs. The
lateral processes for the insertion of the legs are comparatively long; the abdomen is
short and stout.

The proboscis is short and conical, and has a very small mouth at the extremity. The
mandibles are rather stout. The basal joint is constricted at the base, and indistinctly
divided into two joints, it is nearly as long as the proboscis ; the second joint is placed at
right angles with the basal joint, and is considerably swollen and stout. At the
extremity it is furnished with two claws, one straight, pomted and immovable, the other
curved and movable, but also pointed. The inner surface of these-claws is smooth, but
there is a blunt point in the middle of the movable claw.

The ovigerous legs of the female specimen (the only one dredged) are not very
strong. The first three joints are small, the fourth and the fifth are the longest, nearly
of the same length and a little curved. The sixth joint is not quite half as long’ as the
fifth. The four last joints are but little shorter than the sixth. This claw is, compar-

REPORT ON THE PYCNOGONIDA, 79

atively strong: itis not denticulated on the inner surface but slightly serrated. The joints
of the ovigerous legs are almost quite smooth. The shape of the denticulate spines is
very curious. They are broad and flat, have two or three stronger teeth on each side
near the base, and extremely fine teeth all over the rest.

The very smooth legs are comparatively long. The first and the third joints are short and
almost of equal length, the second joint is more than twice as long, having a large oval
genital opening at the extremity on the ventral surface. The fourth joint, containing the
ovary, is considerably swollen and very long ; the fifth is only a little shorter, the sixth,
on the contrary, is a little longer. The two tarsal joints are very small, together about one-
fifth of the length of the sixth joint. Almost every joint describes a feeble but character-
istic curve ; especially the second, the fourth and the eighth joint. The first tarsal joint
is extremely small, and is furnished with a,large number of hairs and an isolated stronger
spine, the second tarsal joint also shows a number of hairs and four stronger spines
opposite to the claw. The claw is strong and very long, considerably curved, and with-
out auxiliary claws. :

The only specimen of this species dredged during the cruise of H.M.S, Challenger
is a female, which, I think, is a full-grown one.

Habitat.—This species, along with a specimen of Pallene australiensis, Hoek, was
collected at Station 162. April 2, 1874. Off East Moncceur Island, Bass Strait. Depth
of the sea, 38 to 40 fathoms. Bottom of the sea, sand.

Observations.—This very characteristic species may be easily recognised among the

" different species of Pallene by the form of the proboscis and cephalothoracie segment, by

the shape of the denticulate spines of the ovigerous legs, by the presence of a claw at the
end of the ovigerous leg, and finally by the absence of auxiliary claws at the end of
the legs.

Pallene langwda, un. sp. (Pl. XII. figs. 1-5).

Diagnosis.—Body highly concentrated, rather disciform. Proboscis conical,
cephalothoracic segment comparatively long. Ovigerous legs with denticulated spines,
but without a claw. Legs without auxiliary claws. Oculiferous tubercle conical, elevated.
Rudiments of palpi in the form of knobs.

Description.—
Length of the proboscis, ; " - é : : 5 0°45 mm,
Length of the trunk, : ; ; B : : c : Ii)
Total length of the body, : 0 : i 5 ; : Ws
Length of the ovigerous leg, : ; : ~* ; : : 223)
Length of the leg of the third pair, ; < : * ; Olina.

Of this curious species, unfortunately, only a single specimen was collected, and this
specimen had, moreover, suffered much from the alcohol ; it is visibly crumpled, especially

80 THE VOYAGE OF H.M.S. CHALLENGER.

on the cephalothoracic segment, as seen from the dorsal side; the other segments have
also suffered in a less degree, which makes it very difficult to judge of the original form.

The proboscis is small, obtusely conical; the mouth is small, as in the other species
of this genus. The cephalothoracie segment is considerably swollen anteriorly, where
it bears the proboscis and the mandibles; in the middle it is constricted so as to form
a neck, and posteriorly it becomes wider again. This wider part (the thoracic part
of the cephalothorax) bears the conical oculiferous tubercle, which shows only rudi-
mentary eyes. The cephalothoracic segment seems, like the two following segments, to
get considerably wider posteriorly on the dorsal surface, thus forming large folds in the
breadth above the insertion of the first three pairs of legs. The fourth thoracic segment
is quite flat; the lateral processes for the insertion of the legs are extremely short. The
abdomen is very small but comparatively broad. .

The surface of the body is smooth ; on the mandibles, the ovigerous legs, and the legs,
numerous not very long but spiny hairs are observed. The first joint of the mandibles
reaches as far as the tip of the proboscis, The second joint is not very strong, is furnished
with slender pincers, and is armed on the inner side with four short teeth. Rudiments of
palpi are implanted ventrally near the base of the mandibles; they are only one-jointed
knobs.

The ovigerous legs are short, little longer than the body. The first three joints are
short; the two following joints are much longer ; the fifth is the longest and is armed near
the distal extremity with a small knob; the sixth joint is short. Of the four following
joints the first is the longest, the last three are nearly of the same length. There is no
claw at the end of the tenth joint. The denticulate spines of one and the same joint
are by no means all of the same shape, those placed near the preceding joint are a great
deal smaller than those in the middle of the row, whereas those placed at the end of the
row are the largest of all, and are furnished at the base with three strong teeth of which
the third especially is very large (fig. 5).

The length of the legs is almost three times the length of the body. The first three
joints are small ; the three following are much longer, but not very slender. The seventh
joint is extremely short; the second tarsal joint is nearly six times as long. Besides the hairy
spines on all the joints, which, as far as I could ascertain, are scattered rather irregularly over
the surface, the last joint has, on the inner side, a row of short and comparatively strong
spines. The claw at the end of the leg is long and stout. Auxiliary claws are wanting.

Of this species only a single specimen was obtained during the cruise of the Challenger,
and, judging from the knobs at the end of the fifth joint of the ovigerous leg, I consider
it to be a male.

Habitat.—Pallene languida was dredged at

Station 161. April 1, 1874. Off the entrance to Port Philip (Melbourne, Australia).
Depth of the sea, 38 fathoms. Bottom of the sea, sand.

REPORT ON THE PYCNOGONIDA. 81

Observations.—This species is in all probability nearly allied to Pallene longiceps,
Bohm (Sitzungsberichte der Gesellsch. Naturf. Freunde in Berlin, 1879, p- 59). However,
as no figure of Béhm’s species has ever been published, and as the description of it
cannot be entirely applied to my specimen, I thought it safer to consider, and to describe
this as a new species,

Pallene longiceps, Bohm, has rudimentary two-jointed palpi, and a short and blunt
oculiferous tubercle. Moreover, the form of the denticulated spines of the ovigerous
legs of the present species is different from the form described by Bohm for his Pallene
longiceps. The latter species is from Japan, whereas my Pallene languwida was obtained
in the vicinity of Melbourne.

Phoxichilidium, Milne-Edwards.

Phoxichilidium fluminense, Kroyer (Pl. XIV. figs. 1-4),

Phoxichilidium fluminense, Kroyer, Bidrag til Kundskab, &c., Naturh. Tidskr. Ny Raekke, vol. i.
p. 124, 1845, Tab. i. fig. lof,

Pallene jfluminensis, Kroyer (sp.), Bohm, Pyenogoniden des Museums zu Berlin, Monatsbericht
der k. A. der Wissensch. zu Berlin, Februar 1879, p. 180, Taf. i. fig. 4-47.

This species has been described and figured by Kréyer (Joc. cit.), and again by Bohm
(Joc. cit.). It may not, however, be considered superfluous to publish new figures ; those
of Kroyer are in general highly characteristic, but they are, as regards the details, not
very exact; from Béhm’s figure, which has been drawn on much too small a scale,
nobody, I think, would recognise the species.

The description given by both authors is nearly correct. The basal joint of the
mandible reaches farther than the tip of the proboscis; it shows dorsally a little
beyond the middle a slight angle, furnished with a row of stronger hairs: therefore
the joint seen from the dorsal surface seems to be divided into two. Rudiments
of palpi are present in the form of rounded knobs on both sides of the cephalic
segment. The ovigerous legs of the full-grown animal are ten-jointed; I have figured
joints six to ten in fig. 3. The sixth jomt shows a wreath of short strong spines imme-
diately before the articulation with the seventh joint. The seventh to the tenth joints are
armed with curved spines and strong hairs, but no denticulate spines at all are present.
These last five joints of the ovigerous leg are very curiously bent in the form of an §, as
has been correctly observed and drawn by Kroyer. The legs are comparatively stout. The
only specimen of this species brought home by the Challenger is a male, with rounded,
rather large genital openings, which, as far as I could ascertain, are present only on the
ventral surface of the second joint of the two hindermost legs. The fourth joint of the
leg is more than twice as long as the second, and not inconsiderably swollen in the
Challenger specimen ; ventrally a little in front of the middle it is furnished with a
distinct and comparatively strong tubular process, which in all probability communicates

(zooL. CHALL. EXP,—PART x.—1881.) K ll

82 THE VOYAGE OF H.M.S. CHALLENGER,

with a gland situated in the interior of the jomt. This tubular process has been observed
neither by Kréyer nor by Béhm. Probably it occurs only in the male sex. The fifth
joint is as long as the fourth, the sixth a little longer. The first tarsal joint is short, the
second comparatively long, armed with a claw and two long auxiliary claws. Joints one
to four have only a few hairs, while joints five to eight are covered by numerous, and
for the most part, comparatively long and stout hairs.

Habitat.—This species, according to Kréyer, is found off Rio de Janeiro, whereas
Béhm describes specimens collected by the German man-of-war, the “Gazelle,” in the
Straits of Magellan, and on the Patagonian coast, at a depth of 30 to 42 fathoms. One
specimen was dredged by the Challenger off Bahia. Depth, from 7 to 20 fathoms.

Observations.—Béhm considers:this species a Pallene. I think, however, there can
be no doubt that it is a true Phowichilidium in the sense of Kroyer. To take the num-
ber of joints of the ovigerous legs as a decisive proof in this matter is, I think, not
safe. The ovigerous legs of the Pallene (Pallene lappa, Bohm) which Bohm examined,
were only seven-jointed, and for that reason alone the specimen cannot be considered
as a Phoxichilidium. Of much greater value, I think, is the form of the ovigerous leg
itself, the form of the last joints, of the spines with which they are furnished, &c., also
the whole form of the body, the manner in which the cephalic part of the cephalothoracic
segment overhangs the proboscis, &c.

Another question is, of course, whether it would not be convenient to class as a separate
genus those forms of Phoxichilidiwm which have ten-jointed ovigerous legs, probably
always present in both sexes. But before taking this step, the different forms ought to
be better known, and for this a close study of full-grown specimens of both sexes is neces-
sary. The genus Anoplodactylus of E. B. Wilson cannot be accepted, because neither
the presence or absence of auxiliary claws, nor the fact of the ovigerous legs being five-
or six-jointed, has any real importance.

Phoxichilidium insigne, n. sp. (Pl. XIV. figs. 5-7).

Diagnosis.—Body slender, with large intervals between the lateral processes. Pro-
boscis cylindrical, inserted ventrally far posteriorly between the two ovigerous legs. Man-
dibles two-jointed, the first joint bearing the second laterally. Ovigerous legs six-jointed.

No auxiliary claws, Legs and mandibles furnished with large conical knobs.
Description.—

Length of the proboscis, 2 mm.
Total length of the body, . ‘ é : 3 é Go ai
Length of the abdomen, ‘ : f ‘ ; , : Ober
Length of the ovigerous leg, : : i : : 5 4:2 ,,
Length of the leg of the first pair, . ; : 5 F ; 19

Of this most curious form, unfortunately, only a single specimen—and that much

REPORT ON THE PYCNOGONIDA. ; 83

mutilated, with only five legs—was collected during the voyage of the Challenger. This
specimen is, I think, a full-grown male. The body is extremely slender, with very large
intervals between the lateral processes for the insertion of the legs. The cephalo-
thoracic segment is rather short, about twice as long as the first true thoracic segment ;
the second thoracic segment isa little longer than the first, and the third is, again, a little
shorter. The proboscis is long, inserted ventrally, far back between the two ovigerous legs.
Tt shows a little swelling at its base, in the middle, and again at the extremity. The
mouth is small and triangular. The abdomen is short and directed somewhat upwards.

At the base of the mandibles the front part of the cephalothoracic segment is
for a short distance cloven in the middle. Immediately behind this cleft the blunt
oculiferous tubercle, with its four dark eyes, is placed. The basal joints of the mandibles
diverge considerably, and extend beyond the front of the proboscis. The end of this basal
joint, which is directed forwards, terminates in a pointed appendage, and laterally, under-
neath the end of this appendage, the short second joint is attached. This has the form
of a bird’s head with the small pincers as jaws. The inner surface of these pincers is
smooth. The first joint towards its extremity and the whole surface of the second joint
are covered with numerous long hairs.

The ovigerous legs are inserted close to the base of the proboscis; they are six-jointed;
the first joint is small, the second about half as long as the proboscis, the third nearly as
long as the proboscis, the fourth half as long as the second, the fifth a little shorter than
the fourth, and the sixth extremely small. All the joints are furnished with numerous
small hairs; those on the two last joints are a little longer, but still extremely slender.

The first joint of the legs is small, nearly as long as the lateral process, the second joint
is more than twice as long as the first, the third joint nearly half as long as the second,
the fourth is as long as the trunk with the abdomen, the fifth is but little shorter, the
sixth is as long as the whole length of the body, the seventh is short, and the eighth
nearly as long as the second joint. The part of the eighth joint facing the strong claw
has a distinct shoulder, furnished with spines and small hairs. The first joint of the
leg bears at the distal extremity, on both sides, a strong conical protuberance; the second
bears a still larger one ventrally, and another at the: distal extremity ; the third, too,
is furnished with one. Besides three strong protuberances at the distal extremity, the
longest of which is placed between the two others, the fourth joint has three other
protuberances placed laterally on the joint; one of these is placed in the middle, the two
others on the other side at equal distances from the middle one. The protuberances at
the extremity of the joint are much larger than the others found on the joint. The
latter have, moreover, a slender spine at the top. The armature of the fifth joint is
nearly the same as that of the fourth. The sixth joint is furnished with numerous small
protuberances, bearing slender spines at the top. Distinct hairs are seen on all the
joints ; towards the fourth joint they grow stronger and denser. The side of the last

84 THE VOYAGE OF H.M.S. CHALLENGER,

joint facing the claw when it is closed is furnished, in addition to numerous slender
spines, with a row of curiously-shaped teeth (see fig. 7 of Pl. XIV.). The last joint
terminates in a strong protuberance, like those placed at the extremities of the other
joints of the leg. The claw is long and stout ; auxiliary claws are wanting.

I think the only specimen of this species dredged by H.M.S. Challenger is a male.
I could not, however, ascertain the sex without injuring the specimen, and I can only
state my supposition. It is based on the fact that there are species of Phoaichilidiwm
in which six-jointed ovigerous legs are present only in the male, and also on the pre-
sence of dermal glands in the fourth joint of the leg.

Habitat.—This curiously-shaped Pyenogonid was dredged off Bahia at a depth of 7
to 20 fathoms.

Observations.—I think this species of Phowichilidium is a near relation of the European
shore and shallow-water forms of the same genus (Phoaichilidium femoratum, P. virescens,
&c.) ; from these it can be easily distinguished by the extremely characteristic protuber-
ances on the legs, mandibles, &c.

Phowichilidium patagonicum, n. sp. (Pl. XIL. figs. 6-9).

Diagnosis.—Body robust, lateral processes scarcely separated. Basal joint of the
mandibles indistinctly divided into two joints, second joint short, with small pincers.
Palpi represented by large rounded knobs. Ovigerous legs ten-jointed, without claws,
present in both sexes; auxiliary claws on the legs. Abdomen long.

Description.—Of this species a full-grown female and two small specimens, about
whose sex I do not feel quite sure, were dredged by H.M.S. Challenger. For the
description I have made use of the full-grown female.

Length of the proboscis, . i : . ° ; 5 6 mm.
Total length of the body, . . ‘ : E : : 116 Ses
Length of the abdomen, : F : : ¢ . . Das
Length of the ovigerous legs, ; : ¢ : 5 : ey;
Length of the leg of the third pair, . ¢ f : ‘ : BH fe oc

The body of this species is almost entirely smooth; the cephalothoracic segment,
which is not quite so long as the abdomen, bears the oculiferous tubercle quite at the
front. The two following thoracic segments are together not quite so long as the cephalo-
thoracic segment. The last segment is very small, it bears a long abdomen directed
upwards. The length of the lateral processes is very considerable.

The proboscis is ventrally inserted, its base is found considerably behind the front
margin of the cephalothoracic segment. It is comparatively long, and its shape is cylin-
drical ; the extremity is rounded, with a small triangular mouth.

The mandibles are inserted close to each other and have a very long basal joint,

REPORT ON THE PYCNOGONIDA, 85

which, seen from the dorsal side about the middle, shows a distinct articulation. This
basal joint is considerably swollen at the extremity ; the second joint is directed towards
the ventral side, while its pincers are bent laterally, so as to be directed towards those of
the other mandible. These pincers are smooth and extremely short. While the basal
joint of the mandibles is nearly smooth, the second joint is furnished with numerous and
strong hairs, which are a little stronger still at the base of the pincers.

The palpi are represented by large rounded tubercles, placed at both sides of the
base of the proboscis.

The ovigerous legs are comparatively short (at least in the female). The first joint
is very small, the second is elongated and not quite three times as long as the first, the
third is again short, the fourth and fifth joints are longer, the sixth is only two-thirds the
length of the fifth, and the last four joits are small. They are figured on Plate XII. fig. 8,
and are covered with long spiny hairs. There is no claw at the end of the tenth joint.

The first jomt of the legs is small, the second is more than twice as long, and be-
comes considerably thicker towards the extremity, the third joint is only a little longer
than the first, the three following are about the same length ; the fifth joint, however, is
the smallest, the sixth the longest. This joint in the second leg of the right side describes
a shght curve, which at the convex side is surmounted by a strong conical protuber-
ance. I think, however, there can be little doubt that this conical protuberance is to be
considered as an accidental outgrowth caused probably by the joint having been broken
and afterwards healed. The first tarsal joint is very short, and the second is about as long
as the second joint of the leg. At its extremity the last joint bears a comparatively
feeble claw and two auxiliary claws. The joints of the legs have numerous but small
and stout hairs; they are at the swollen extremity of the second joint, and on the third
and the fourth joints; on the following joints they are much more numerous, but also
a great deal more slender. On the two last joints, which have also stronger spines, for
example on the side facing the claw, they are most numerous of all.

The female specimen shows very large genital pores at the considerably swollen distal
extremity of the second joint of the leg. They are found ventrally on all the legs. The
specimens seem to be very brittle, especially the younger ones, which had lost nearly all
their legs.

Habitat.—This species was collected at three different stations not far from the coast
of Patagonia. ;

Station 304. December 31, 1875. Lat. 46° 53’ S., long. 75° 11’ W. Depth of the
sea, 45 fathoms. Bottom of the sea, sand.

Station 308. January 5, 1876. Lat. 50° 10’ S., dong. 74° 42° W. Depth of the
sea, 175 fathoms. Bottom of the sea, mud.

Station 313. January 20,1876. Lat. 52° 20’ S., long. 68° 0 W. Depth of the
sea, 55 fathoms. Temperature at the bottom, 8°8° C. Bottom of the sea, sand.

86 THE VOYAGE OF H.M.S. CHALLENGER.

Observations.—In general, the shape of this Pyenogonid resembles that of Phoxichili-
dium digitatum, Bohm. However, in many respects, it may be easily distinguished from
this and other species of Phoxichilidium hitherto described ; for instance, by the presence
of ovigerous legs in the female, by the presence of auxiliary claws, by the number of
joints (10) of the ovigerous legs, &e. Like most other species of the same genus, this
species seems only to occur in shallow water (depth 45 to 175 fathoms) not far from the
coast.

Phoxichilidium patagonicum, var. elegans, n. var..(Pl. XII. fig. 10).
Diagnosis.—Like Phoxichilidium patagonicum, Hoek, only much more slender.
Description.—

Length of the proboscis, . . é : : : 3°5 mm.
Total length of the body, . th ; : i ‘ ; O° 5
Length of the abdomen, . ‘ Din te.
Length of the leg of the third pair, . 28°53
Length of the ovigerous leg, . eee

A young specimen has the different thoracic segments by no means so concentrated
or robust as is the case in the specimens of Phowichilidium patagonicum ; the lateral
processes are much more widely separated; in general the length of the body, in com-
parison with that of the legs and of the proboscis, is much more considerable. The oculi-
ferous tubercle is furnished with four eyes, but the two foremost are much larger than
the two others. The length of their legs and their joints is not very different from that of
Phowxichilidium patagonicum ; the only difference being that the total length is compara-
tively less. The claws and the auxiliary claws are as in Phowichilidium patagonicum.
About the sex of this specimen I do not feel quite sure : most probably it is a young female.

Habitat.—Station 320. February 17, 1876. Lat. 37° 17’ S., long. 53° 52’ W.
Depth of the sea, 600 fathoms. Bottom temperature, 2:7° C. Bottom of the sea, hard
ground. 7

Observations.—The single specimen of this form resembles Phowichilidium pata-
gonicum so strongly that I hesitated long whether or not I should consider it as
specifically distinct. My study of other species, younger and older specimens, has
convinced me that, as a rule, as the animal advances in age, its slenderness increases.
Now, in the present case, a young specimen shows considerable slenderness, while
the full-grown female is much more concentrated. That it is a young specimen is proved
by the rudimentary condition of the ovigerous leg. I therefore feel inclined to consider
this form as a variety of my Phoxichilidium patagonicum. Considering the difference
in depth of the stations at which that species and the present form were dredged, we
have here most probably an instance of the influence of surrounding circumstances on the
form of an animal.

REPORT ON THE PYCNOGONIDA, 87

Phoxichilidium molhssimum, n. sp. (Pl. XIII. figs. 6-9),

Diagnosis.—Body robust, lateral processes not very widely separated. Mandibles
distinctly three-jointed, with curved, smooth, and not very long pincers. Ovigerous legs
ten-jointed, without claw (probably present in both sexes). Auxiliary claws (2). Palpi
represented by small rounded protuberances. Legs with silky hairs.

Description.—
Length of the proboscis, , , . . 5 ’ c 9:5 mm.
Total length of the body, . 6 : i ; : : QSriyas
Length of the abdomen, . 5 : e4 TL : . OF ns,
Length of the ovigerous leg, C ; : ; : : ZO ss
? Length of the first six joints of the leg, . ; : 5 : BOR ss

Of this interesting deep-sea Pycnogonid, unfortunately only a single specimen
(much injured) was collected during the voyage of H.M.S. Challenger. There is not
a single complete leg; and of the incomplete ones, with their three joints, there are in
all only three present. However, this form is so highly characteristic that I think it
possible to give, even from this defective specimen, a description which will be recognised
by future investigators.

The body is robust; like the proboscis, the lateral processes, and the first joints of the
legs, it is entirely smooth. The front of the cephalothoracie segment projects over
the base of the proboscis. This front part bears dorsally the blunt oculiferous tubercle,
with its rudimentary eyes, and quite anteriorly the large mandibles are inserted. These
run parallel to one another, and are distinctly three-jointed. The basal joint is com-
paratively long, swollen at its base, and again at the extremity; the second is about
two-thirds the length of the basal joint; the third joint is very short, and terminates in
a pair of smooth, strongly-curved pincers, which, when closed, have a wide interval
between them.

The proboscis is very stout, swollen a little in the middle, and also at the extremity ;
seen laterally, the swelling at the extremity appears rather stronger on the dorsal than
on the ventral side. The triangular mouth is quite closed by the labial plates. Near
the base of the proboscis the cephalothoracic segment bears on both sides a small blunt
protuberance, which represents the palpus. é

“The ovigerous legs are inserted ventrally. Seen from that side, the cephalothoracic
segment is distinctly divided into two segments, and the ovigerous legs originate from
the first of these two segments. They are inserted on small processes, which represent
the lateral processes of the ovigerous legs, and have ten joints. The first and third
joints are short; the second is about twice as long; the fourth is comparatively stout and
longer than the second; the fifth is as long as the second, and much more slender
than the fourth; the sixth is shorter than the fifth, slender, but swollen at the extremity.
The last four joints do not show any great differences in length; however, from the

88 THE VOYAGE OF H.M.S. CHALLENGER.

sixth to the tenth each joint is more slender than the preceding one. The hairiness of
the different joints of the leg is not very great. Some hairs are found on the second to
the sixth joints, the latter haces especially at the swollen extremity, furnished with
some stronger hairs. The seventh joint is, near the extremity, armed with very long
hairs; the eighth joint has them all over the surface; on the ninth joint the hairs are
short and few; while the very slender tenth joint is furnished not only with some short
hairs, but also with rows of stronger spines.

The lateral processes for the ies of the legs are comparatively long. The abdo-
men is very long, being nearly cylindrical, and at the extremity a little swollais

The second joint of the leg is twice as long as the first and the third. Of the three
following joints, which are comparatively long, the first is a little longer than the second,
and a little shorter than the third. With the exception of a row of not very nume-
rous hairs placed at their extremities, the first three joints are smooth; the fourth
shows already a small number of very thin hairs, which are much more numerous on
the fifth, and extremely numerous on the sixth joints. On these last two joints, however,
the hairs cover only half the surface longitudinally, whereas the other half has slender
spines placed in distinct rows (fig. 9).

The single specimen of this species shows ventrally small genital pores on the second
joint of the first, second, and third legs (the only legs riteaent); From the smallness of
these genital pores, the absence of ovaries in the fourth joint of the leg, and the shape of
the ovigerous legs, I conclude that this specimen is a male.

Habitat.—The single specimen was brought up from

Station 237. June 17, 1875. Lat. 34° 37’ N., long. 140° 32’ E. Depth of the sea,
1875 fathoms. Bottom temperature, 1°7° C. Bottom of the sea, mud.

Observations. —This species and the two following (Phowichilidiwm oscitans, Hock,
and Phoawichilidium pilosum, Hoek) are nearly allied. They are furnished with ten-
jointed ovigerous legs, present in both sexes, and three-jointed mandibles. The late Dr
R. von Willemoes-Suhm erroneously mentioned these species as belonging to the genus
Zetes, Kroyer. When comparing these species with true three-jointed mandibles,
with Phowichilidium fluminense, Kroyer, with two-jointed mandibles, and a distinet
row of spines dorsally near the middle, and with Phowxichilidium patagonieum,
Hoek, which has the basal joint divided into two when seen from the dorsal surface,
and quite undivided when seen from the ventral surface, it becomes evident that
this division, even when so distinctly developed as is the case with Phowichilidium
mollissimum, Phowichilidium oscitans, and Phowichilidiwn pilosum, does not justify
us in considering these species as belonging to a different genus. Even should this
be proposed, they could never be considered as species of Zetes; for that genus
has ten-jointed palpi, whereas these organs in the present forms have become entirely
rudimentary.

REPORT ON THE PYCNOGONIDA. 89

Phoxichilidium oscitans, n. sp (Pl. XILL. figs. 1-5).

Diagnosis.—Body robust, lateral processes not very widely separated. Mandibles
three-jointed, with long and slender pincers. Ovigerous legs ten-jointed, without claws,
probably present in both sexes. Auxiliary claws present. Palpi represented by rounded
protuberances. Proboscis swollen in the middle, and considerably at the tip.

Description.—
Length of the proboscis, . : F : , : ‘ 8 mm.
Total length of the body, . 7 F 5 i? ; 21°'5 ,,
Length of the abdomen, . ‘ ‘ : ‘ 5 F O:Dis,
Length of the ovigerous leg, ' ; , : : F 9:61,
Length of the leg of the third pair, i F ‘ ore;

A single specimen of this beautiful species was brought home by the Challenger. It
is a species with a robust body, with long lateral processes, which are not widely
separated, a very long abdomen, and a very stout proboscis. The first or cephalic part
of the cephalothoracic segment is almost globular, and bears about its middle a blunt
oculiferous tubercle with two rudimentary eyes, represented by brown spots, which are
connected by a slender strip of pigment, the whole not unlike the form of what the
French call a pince-nez. The cephalothoracic segment is nearly as long as the three
other segments together. The abdomen is long, cylindrical, swollen at the extremity.

The proboscis is very stout; it is considerably swollen in the middle, and also at the
extremity. This extremity is flattened at the front, and has a very large triangular
mouth, the three lips of which are turned inwards. While the body is almost everywhere
smooth, the front of the proboscis bears round the mouth not very long but comparatively
strong hairs.

The mandibles are distinctly three-jointed. The first joint is the longest; the
second is but little shorter; together they reach considerably beyond the end of the
proboscis. The third joint is small, and bears a pair of extremely slender pincers, the
movable one being much more strongly curved than the immovable one. At the end of
the first joint a row of not very long but comparatively strong hairs is observed; those
at the extremity and over the whole surface of the third joint are a little longer. The
pincers are quite smooth.

The palpi are represented by very large globular protuberances, placed at both sides,
near the base of the proboscis.

The ovigerous legs are inserted ventrally not far from each other. Seen from the
ventral side, the cephalothoracic segment is much shorter than when observed dorsally;
nor is there from that side any trace of a division into two joints to be seen, as is the
case in Phoxichilidium mollissimum, Hoek.

The length of the joints of the ovigerous legs is exactly as in Phoxichilidium

(z0oL, CHALL, EXP.—PART x.—1881.) K 12

90 THE VOYAGE OF H.M.S. CHALLENGER.

mollissimum ; the first and third joints are short, the second is a little longer, the fourth
longest of all and much thicker; the fifth joint is only a little shorter than the fourth, but
considerably more slender; the sixth again is a little shorter than the fifth, and swollen
at the distal extremity. The last four joints are short ana nearly of equal length. The
hairs on these last joints are not so long, but more regularly spread over the surface, than
is the case in Phoxichilidium mollissimum. The tenth joint, however, shows nearly the
same row of spines and the same short hairs as in the foregoing species.

The legs are very long. The relative length of the joints is the same as in Phowi-
chilidium mollissimum. The seventh joint is short; the eighth joint is a little curved.
Both these joints are slender; together they are nearly equal in length to the second joint
of the leg. The claw is very long, and furnished with two small auxiliary claws. That
side of the eighth joint which faces the claw shows a row of stronger spines, the last
of which is considerably longer than the others. Besides distinct rows of stouter hairs
at the extremity of the joints, the number of hairs on the surface of the joints con-
siderably increases from the fourth joint downwards, the greatest number being found
on the distal part of the sixth joint.

The only specimen is probably a male. Its genital openings are small, and are
placed ventrally on the second joint of every leg.

Habitat.—This beautiful deep-sea species was found at

Station 70. June 26, 1873. Lat. 38° 25’ N., long. 35° 80° W. Depth of the sea,
1675 fathoms. Sea bottom, globigerina ooze.

Observations.—This species is nearly allied to the foregoing (Phowichalidium mollissi-
mum, Hoek), and also to the following species (Phowichilidium pilosum, Hoek). It may,
however, be easily distinguished from these species by the form of the proboscis and
of the cephalothoracic segment, and by its extremely long legs.

Phoxichilidium pilosum, n. sp. (Pl. XIIL. fig. 10-13).

Diagnosis.—Body not very robust, lateral processes widely separated. Mandibles
distinctly three-jointed, with small straight pincers, Ovigerous legs ten-jointed, without
claws, present in both sexes. Auxiliary claws present. Palpi represented by rounded
protuberances. Proboscis cylindrical, tapering towards the extremity. Body (dorsally)
and legs covered with extremely long and thin hairs.

Description.—

Length of the proboscis, 5 mm.
Length of the abdomen, - : : : : . De
Total length of the body, ‘ : ; A F é j Dine.
Length of the ovigerous leg, . ; : : ; : ; Sass
Length of the leg of the third pair, . : ; 5 : : 44 ,,

Of this species three specimens were collected during the cruise of H.M.S. Challenger;

el

REPORT ON. THE PYCNOGONIDA. 91

there are two females and a male. ‘The male is a great deal smaller than the larger of
the two females. I therefore give the description from the larger female. The body
is stout, but, as the lateral processes are widely separated, not very robust. The
cephalothoracic segment is not very long. Quite in front of it the oculiferous tubercle
is inserted go as to overhang the base of the mandibles. It is much elevated, conical,
with two larger eyes directed forwards and two smaller ones directed backwards. The
first and second true thoracic segments together are shorter than the cephalothoracic
segment. The last thoracic segment is short, and bears at the extremity a very large
abdomen, the length of which is nearly equal to that of the proboscis. The abdomen is
a little swollen at the tip. Dorsally the surface of the body of the lateral processes and
of the abdomen is furnished with very slender hairs, of which a distinct row is observed
on the hinder margin of the different thoracic segments.

The two mandibles are three-jointed; the first two Joints run parallel to each other,
The first joint reaches as far as the end of the proboscis; the second joint is a little
longer; the third is inserted on the second, with which it makes a right angle. The
pincers of the two mandibles are directed horizontally towards each other; they are placed
at a short distance from the end of the proboscis, are straight, and very short.

The proboscis is cylindrical, tapering towards the extremity, where the small mouth
is situated. At the base of the proboscis the two protuberances representing the palpi
are inserted,

The ovigerous legs are ten-jointed: the first and third joints are very small; the
second is about twice as long; the fourth and fifth are the longest of all; the sixth joint
is short; and of the four last joints the second is the longest and the last the shortest,
They are covered with not very long but thin hairs, rows of stronger ones, as a rule,
being found at the extremity of the joints.

The second joint of the legs is nearly twice as long as the first or third, and in the
female considerably swollen at the extremity. The fourth joint is also considerably
swollen in the female, and is longer than the first three joints together. The fifth
joint is much more slender and also a little shorter than the fourth; the sixth is much
longer and, at the same time, a great deal more slender. The two last joints together are
not quite one-third the length of the sixth joint. The first tarsal joint is extremely short,
the second about five times as long. From the first to the sixth all the joints are covered:
with very long and slender hairs, giving an extremely woolly appearance to the whole
animal. The first tarsal joint is furnished with numerous stronger and smaller hairs; the
second shows a row of distinct spines, the last of which is the largest, while the others
diminish in size. The claw at the end of the leg is very large; it is accompanied by two
extremely small auxiliary claws.

The females have very large genital openings ventrally on the swollen extremity of the
second joint of all the legs. In the males I could observe the small genital pores only

92 THE VOYAGE OF H.M.S. CHALLENGER.

on the ventral surface of the two hindermost legs. They are here placed at the tip of a
small tubercle, which is likewise absent on the two first pairs of legs. The genital pores
of the males are almost quite covered by the surrounding hairs.

This hairy Pyenogonid was dredged by the Challenger at two different stations.

Station 147. December 30, 1873. Lat. 46° 16’ S., long. 48° 27° E. Depth of the
sea, 1600 fathoms. Temperature of the bottom, 0°8° C. Bottom of the sea, globigerina
00ze.

Station 157. March 3, 1874. Lat. 53° 55’ S., long. 108° 35’ E. Depth of the sea,
1950 fathoms. Bottom of the sea, diatom ooze.

Observations.—The near relation which this beautiful deep-sea species bears to the
two foregoing ones is evident. They form the true deep-sea representatives of the genus
Phoxichilidium, Milne-Edwards, which probably will be found to have an extremely
wide range.

Hannonia, nu. gen,

Diagnosis.—Proboscis stout, inserted quite in front of the cephalothoracic segment.
Mandibles rudimentary, small, two-jointed, chelate. Palpi wanting. Ovigerous legs,
present in both sexes, ten-jointed.

Hannonia typica, u. sp. (Pl. XIV. fig. 8-11).

Diagnosis.—Body robust, proboscis long-ovate, truncated at the tip, and forming a
narrow stalk posteriorly. Legs short, with a small first tarsal jot and a claw, without
auxiliary claws. :

Description.—
Length of the proboscis, ; 5 5 : : 5 : 4 mm.
Length of the trunk with the abdomen, ; : : : : Ua
Total length of the body, : ; F ; : : : TT
Length of the leg of the third pair, . ; : 3 : : Lbs;

This curious sea-spider has a robust body; the cephalothoracic segment is not very
large, and, like the two following segments, its hinder margin is furnished with an
elevated ridge; on these ridges a row of small hairs is inserted. The oculiferous
tubercle is blunt, and placed in the middle of the cephalothoracic segment. It is
furnished with four comparatively large black-coloured eyes. The dorsal surface of the
lateral processes, like that of the last thoracic segment immediately in front of the inser-
tion of the abdomen, shows rounded protuberances, on the surface of which small hairs—
like those of the ridges on the hinder side of the thoracic segments—are placed.
The abdomen is not very long, but stout and swollen at its extremity. Its surface is
likewise covered with numerous small hairs. The form of the proboscis is ovate; at the
anterior end it is flattened and truncated. The mouthis found in the middle of this trun-
cated surface; it is triangular, with comparatively large lips. At the back the proboscis is

REPORT ON THE PYCNOGONIDA. 935

narrower, the narrow part thus forming a sort of stalk-like process on which the ovate
front part is borne. The surface of the proboscis, when seen with the naked eye or
slightly magnified, is entirely smooth.

The mandibles are small and rudimentary ; they consist of a short basal joint and a
quite rudimentary second joint, armed with rudimentary pincers. The length of the
mandibles is about one-fourth the length of the proboscis.

The ovigerous legs are not very strong; they are ten-jointed. The first three joints
are short; the fourth and the fifth joints are the longest; the sixth is about two-thirds
the length of the fifth; and of the last four joints the first is by far the longest, and the
third the shortest. A small claw is found at the extremity of the tenth joint. All the
joints are furnished with small hairs; the last four joints are not armed with denticulate
spines, but with not very strong straight spines, scattered rather irregularly over the
whole surface of the joints.

The legs are short. The first three joints are extremely short; the three following
are longer and nearly of the same length, which is shorter than that of the first three
joints together. The first-tarsal joint is very short; the second comparatively lone and
feebly curved, it bears at the extremity a small strongly-curved claw, which is sickle-
shaped, and not accompanied by auxiliary claws. All the joints of the legs are furnished
with numerous minute spines, placed in regular rows; the fifth and sixth joints, however,
are also armed with a distinct row of tubercles, each bearing a small but strong spine at
the tip (fig. 11).

The only specimen of this species is a female. It has very large genital pores on.the
second joints of all the legs. The ovaries are found reaching as far as the sixth joint of
the leg. The ovarian eggs are exceedingly numerous, but comparatively large.

This interesting Pycnogonid was found on the shore at Seapoint, near Capetown.

Observations.—It is a true shore inhabitant, and forms among the species with-
out palpi the transition from those with (Pallene and Phowichilidiwm). to those
without mandibles (Pycnogonwm and Phowichilus). To the first of the latter genera -
(Pycnogonum) it is, I believe, very nearly allied—viz., by the robustness of the body and
by the presence of the protuberances (which I showed in my paper published in 1877,
Ueber Pycnogoniden, to be outgrowths of the skin, richly armed with tactile organs)
on the dorsal surface of the body and of the lateral processes. The want of auxiliary
claws in both genera is also striking. Distinct differences are furnished by the presence
of mandibles, and of ovigerous legs in the female of my Hannonia typica; I have
already pointed out above, however, that I do not consider these differences very
important.

94 THE VOYAGE OF H.M.S. CHALLENGER.

APPENDIX I.

DESCRIPTION OF THE SPECIES DREDGED DURING THE CRUISE
OF THE “ KNIGHT ERRANT.”

During the recent cruise of the ‘ Knight Errant,” organised by Prof. Sir Wyville
Thomson to acquire a more accurate knowledge of the abnormal distribution of tempera-
ture in the Faroe Channel, numerous Pycnogonids were collected by trawling. As this
cruise bears upon the voyage of the Challenger and the study of the results of her
voyage, I was asked to give also a description of these forms for this report.

Nymphon strémi, Kroyer.

Nymphon strémii, Kroyer, Bidrag til Kundskab, &c., Natiirh. Tidskr., N. R., i. 111, 1845.

Nymphon gracilipes, Heller, Crustaceen, Pycnogoniden, und Tunicaten der K. K, Oester.
Ungar. Nordpol. Exped. Denkschr. der Math., Naturw. Classe der Kaiserlichen Akad. der
Wiss., xxxv. 40, 1875,

Nymphon strémii, Kroyer, Miers, Ann. and Magazine, 4th series, vol. xx. p. 109, 1877.

Nymphon gracilipes, Heller, G. O, Sars, Prodromus descriptionis Crustaceorum et Pyenogoni-

darum, quae in expeditione Norvegica, anno 1876, observavit, Arch, f. Math. og Naturvid.,
ii. 265, 1877.

Nymphon stromii, Kroyer, Wilson, Pycnogonida of New England, Transact. Connect. Acad.,
vol, v. p. 17, pl. vi. fig. la-1h, 1880.

This beautiful and distinct species is accurately described by Kroyer, and also by
Wilson. Its synonymy and wide geographical range I have discussed at some length in
the description of the Pycnogonids collected during the two cruises of the Dutch schooner
*“ Willem Barents” in the Barents Sea, which at this moment is in the hands of the
printer, and will be published probably before the end of the year (1880).

The dimensions of the ‘‘ Knight Errant” specimens are much smaller than those of
the specimens described by Heller and myself, and even smaller than those which Wilson
has got from the neighbourhood of the North American coast.

The extent” of the largest “Knight Errant” specimen is not quite 100 mm. The

_ 1 Supplement-Band of the Niederliindisches Archiv fiir Zoologie, Leiden, E. J. Brill.
° “Extent is the distance from tip to tip of the outstretched legs” (Wilson, loc. cit., p. 5).

a

REPORT ON THE PYCNOGONIDA. 95

depth from which this species was brought up is from 515 to 540 fathoms. The stations
where it was found are the following :—

Station No. 5 (cruise of the “ Knight Errant”). Lat. 59° 26’ N., long. 7° 19’ W.
August 11, 1880. 515 fathoms. Warm area. Two specimens.

Station No. 7 (cruise of the “Knight Errant”). Lat. 59° 36’ N., long. 7° 18’ W.
August 12,1880. 530 fathoms. Warm area. Two specimens.

Station No. 8 (cruise of the “ Knight Errant”). Lat. 60° 3’ N., long. 5° 51’ W.
August 17, 1880, 540 fathoms. Cold area. Ten specimens.

In this animal, therefore, we have an example of one inhabiting the cold and
warm areas on both sides of the ridge rising in the Faroe Channel to within 300 fathoms
of the surface." This agrees very well with the facts of the geographical distribution of
our species ; it is a common inhabitant of the depths of the Arctic Sea, but it is also by
no means rare in the deeper water of southern latitudes, especially in the neighbourhood
of the American coast.

Nymphon grossipes, Oth. Fabricius.

Nymphon grossipes, O. Fabricius, Fauna Groenlandica, p. 229, 1780. (See p. 44 of
this report.)

A single specimen of this species was dredged at

Station 8 (cruise of the “ Knight Errant”). Lat. 60° 3’ N., long. 5° 51° W, August
17, 1880. 540 fathoms. Cold area.

For the geographical distribution of this species I refer to the list of species at p. 20.

Nymphon macronyx, G. O. Sars (Pl. XV. figs. 1-7).

Nymphon macronyx, G. O, Sars. Prodromus deseriptionis, &ec., Archiv, f. Math, og Naturvid.,
ii, 265, 1877.

Of this interesting inhabitant of the cold area of the Faroe Channel about thirty
specimens were dredged during the cruise of the ‘‘ Knight Errant.” As hitherto neither a
full description nor any figure of this species has been published, I wish to give both here.

Only a short diagnosis of this species has been published by Professor G. O. Sars.
From this, and from the pencil drawing he had the kindness to send me, the species ‘is
easily recognised. However, in some respects, I observed slight differences from the
diagnosis of Professor G. O. Sars. Probably these will be found to arise from the
fact that the species had been submitted only to a preliminary investigation by the
celebrated Norwegian zoologist.

Nymphon macronyz, G. O. Sars, is a somewhat robust Nymphon, having the second
joint of the palpi longer than the third, the first tarsal joint not quite half the length of

‘the second tarsal joint, and having a very long claw at the end of every leg and

1 Nature, September 2, 1880, C. Wyville Thomson, the Cruise of the “ Knight Errant.”

96 THE VOYAGE OF H.M.S. CHALLENGER.

extremely small auxihary claws. Moreover, it is characterised by a curiously-shaped
oculiferous tubercle. Its dimensions are as follows :—

Length of the proboscis, . ; : : - : 5 2°3 mm.
Total length of the body, 9, . : : : ; ‘ ba ys
Total length of the body, 4, : . ; ; : , Dek 5s
Length of the ovigerous leg, ?, ‘ : : : : : 64 ,,
Length of the ovigerous leg ,g, : : : - ; il Bs
Length of the leg of the third pair, : : : ; ? 13"

The body is almost quite smooth, while the appendages are richly furnished with
hairs. The slenderness of the body is not very great; the lateral processes, however,
are widely separated (Pl. XV. fig. 1). The cephalothoracic segment is shorter than
the proboscis; it is narrow in the middle, while it shows a considerable swelling at
the beginning and at the end. The oculiferous tubercle is situated above the inser-
tion of the ovigerous legs. Seen laterally this shows the conical and pointed shape
described by Professor G. O. Sars; but seen from the front it is considerably flattened
and broad, terminating in two divergent points. It is furnished with four distinct eyes
(Pl. XV. fig. 2). The proboscis is almost quite cylindrical. The abdomen is short.

Of the appendages I have figured the mandibles in fig. 3 on Plate XV. The second
joint is nearly triangular, and almost its whole surface is covered by strong hairs. At
the front, one of the angles of the triangle terminates in the immovable claw, which is a
great deal shorter than the movable one. Both claws bear a row of spines and are
strongly curved at their extremities.

The drawing I have given in fig. 4 of the palpi renders, I believe, a description needless,

The ovigerous leg of the female is shorter and feebler than that of the male; more-
over, it has the fourth and fifth joints quite straight, whereas the same joints in the
male describe distinct curves. The relative length of the joints is the same as in most
other species of the genus Nymphon. In the male the sixth joint is furnished with a
small pointed tubercle, which I did not observe in the female. The males bear the eggs
on the fourth and fifth joints; they are large and collected in one or two packets on both
legs, The four last jomts show a row of denticulated spines of the shape figured on
Plate XV. fig. 5. The claw at the end of the ovigerous leg is strong and pectinated at
the extremity.

The second joint of the legs is twice as long as the first and the third, the fourth
joint is as long as the fifth, the sixth is only a little longer. The first tarsal joint is not
quite half as long as the second. ‘The claw is very long, almost as long as the second
tarsal joint. Very small auxiliary claws, easily overlooked, are situated on both sides ot
the great claw (fig. 7). The second joint of the female is considerably swollen at the
end, where it shows on every leg a large genital pore of an oval shape ; the fourth joint in
the same sex is also swollen. The hairs on the first four joints in both sexes are not
very numerous, whereas, beginning with the fifth, the last joints are richly furnished

REPORT ON THE PYCNOGONIDA. 97

with hairs. The side of the eighth joint facing the claw shows a row of regular strong
spines. The genital pores of the males are smaller than those of the females; they are
present only on the two posterior pairs of legs.

As for the geographical distribution of this species, G. O. Sars dredged it in lat. 62°
44’ 5” N., long. 1° 48’ E., in comparatively deep water (412 fathoms), in the cold area.
He found there only four specimens, whereas a single haul with the trawl in the Faroe
Channel yielded among a thousand specimens of Nymphon robustum, Bell, upwards of
thirty specimens of the species in question. This occurred at

Station No. 8 (cruise of the “Knight Errant ”). Lat. 60° 3’ N., long. 5° 51’ W.
August 17, 1880. 540 fathoms. Cold area.

This station is not very far from the place where it was dredged by Professor G.
O. Sars, and as this is the only instance, so far as I know, of this species having been
collected previous to the cruise of the “ Knight Errant,” most probably it has a very
restricted distribution.

Nymphon robustum, Bell.

Nymphon robustum, Bell, Belcher’s Last of the Arctic Voyages, vol. ii. p. 409, 1855, Tab.
xxxv. fig. 4,

Nymphon abyssorum, Norman, Wyville Thomson, Depths of the Sea, p. 129, 1873.

Nymphon hians, Heller, Crustaceen, Pycnogoniden und Tunicaten der K. K. Oester. Ungar.
Nordpol. Exped. Denkschriften der Wiener Akademie der Wiss., xxxv. 41, 1875.

Nymphon robustum, Bell, G. O. Sars, Prodromus Crustaceorum et Pyenogonidarum, Arch. fiir
Math., og Naturvid., ii. 265, 1877.

An ample discussion of the synonymy of this species, and a description of those
parts of the body which have hitherto been overlooked, I have given in my paper on the
Pycnogonids of the cruises of the “ Willem Barents,” to which I have referred above.
An immense quantity of this true cold area species was dredged during the recent
cruise of the “Knight Errant.” Mr Murray writes to me that this was the greatest
haul of Pycnogonids he ever observed. It is a blind species, and along with it were
trawled a considerable number of specimens of Nymphon macronyx which have distinct
eyes, about ten specimens of Nymphon strémii also furnished with eyes, one specimen of
Nymphon grossipes with eyes, and four specimens of Colossendeis proboscidea, Sabine
(sp.), which is again without eyes. The number of specimens with eggs 1s not very
considerable, and there is not one which shows the numerous highly developed young
ones clinging to the ventral side of the body of their parent as is the case with some
specimens from Barents Sea.

Finally, I wish to point out that the dimensions of the “ Knight Errant” specimens are
considerably smaller than those of specimens from higher latitudes. As I have mentioned
above, this is also the case with the specimens of Nymphon strémii.

(ZOOL. CHALL. EXP.—PART x.—1881.) K 13

98 THE VOYAGE OF H.M.S. CHALLENGER.

A species of Scalpellum, which, so far as I know, has not been observed hitherto,
is a common commensal on the legs of Nymphon robustum, Bell.

This species was dredged at

Station 8 (cruise of the “ Knight Errant”). Lat. 60° 3’ N., long. 5° 517 W. August
17, 1880. Depth of the sea, 540 fathoms. Cold area. Perhaps 1000 specimens.

Station 2 (cruise of the “ Knight Errant”). Lat. 60° 29’ N., long., 8° 19° W. July
28,1880. Depth of the sea, 375 fathoms. Warm area. One specimen only.

This single specimen from the warm area must, most probably, be considered as one
which has strayed from the cold area. As far as I know, the species has not been
observed at a lower latitude than 60° N.

Nymphon robustum, Bell.

Colossendeis proboscidea, Sabine (sp.).

Phoxichilus proboscideus, Sabine, Marine Invertebrate Animals in a Supplement to the Appendix
of Captain Parry’s Voyage for the Discovery of a North-West Passage in the years 1819-
1820, London, John Murray, 1824, p. ecxxvi.

Colossendeis borealis, Jarzynsky, Premissus Catalogus Pycnogonidarum inventarum in mari glaciali
ad oras Lapponie rossice et in mari albo, anno 1869 et 1870. Annales de la Soc. des
Naturalistes de St Pétersbourg, vol. i., 1870.

Colossendeis proboscidea, Sabine (sp.), G. O. Sars, Prodromus descriptionis, &c., Archiv. fiir
Math. og Naturvid., ii. 268, 1877.

Of this interesting species, the first of the genus Colossendeis that was observed, four
specimens were trawled at Station 8, together with many specimens of Nymphon

REPORT ON THE PYCNOGONIDA. 99

robustum, Nymphon macronyx, &e. (See above.) There is one very young specimen,
and the three others are females. For figures and a full description of this species I again
refer to my paper on the Pycnogonids of Barents Sea.!

The specimens trawled by the “Knight Errant” are not quite so large as those from
Barents Sea.

Station 8 (cruise of the “ Knight Errant”). Lat. 60° 3’ N., long. 5° 51° W. August
17, 1880. Depth of the sea, 540 fathoms. Cold area.

Pycnogonum litorale, Strom (sp.).

Phalangium litorale, Strém, Physisk og oeconomisk beskrivelse over fogderiet. Séndmér, belig-
gende in Bergens Stift i Norge, 4°. Sorte, 1762-66, pl. i. fig. 17.

Pycnogonum litorale, O. Faby,., Fauna Groenlandica, p. 223, 1780.

Pycnogonum litorale, Miiller, Zoologia Danica, iii. 68, pl. cxix. figs. 10-12, 1789.

Pycnogonum litorale, Kroyer, Nat. Tidsk. N y Rekke, i. p, 126, 1845.

Of this very common species one specimen was dredged at 53 fathoms. It occurs
only in the neighbourhood of the coast, and ranges to the north as far as the White Sea,
where Jarzynsky (Premissus Catalogus, &c., loc. cit.) collected it on the coast of Russian
Lapland, and as far south as the coast of the Mediterranean. Westward it is common at
different places on the North-American coast, and it also abounds on the east coast of the
Atlantic—as on the English, Dutch, French coasts, &c. Slater (Ann. and Mag. of Nat.
Hist., v. series, vol. iii, 1879) describes a variety of this species—it is a little more
slender—collected on the coast of Japan. Most probably, therefore, the species will also
be found to occur along the whole northern coast of Siberia.

The single specimen trawled in the neighbourhood of the Scottish coast is a male
with distinct ovigerous legs. It was dredged at

Station No. 3 (cruise of the “Knight Errant”). Lat. 59° 12’ N., long. 5. 500 We
August 3, 1880. Depth of the sea, 53 fathoms.

1 This same species has been recently described by Mr E. J. Miers under the name Anomorhynchus smithii,
n. gen., n. sp., from specimens collected by Mr Leigh Smith a little to the south of Franz-Josef Land (Annals and
Magazine of Natural History for January 1881, p. 50, pl. vii. figs. 6-8). (Note inserted during the correction of the
last proof.)

100 THE VOYAGE OF H.M.S. CHALLENGER.

APPENDIX II.

CONTRIBUTIONS TO THE ANATOMY AND EMBRYOLOGY OF THE
PYCNOGONIDA.

Our knowledge of the anatomy and embryology of the sea-spiders is very insufficient ;
of those living in shallow water we know but little, and of the deep-sea forms nothing.
Whereas a prior? it is evident, that in general the deep-sea animals will exhibit the same
anatomical structure, and pass through the same development as the littoral or shallow-
water forms; it is also clear, on the other hand, that a comparison of the anatomy of
animals inhabiting very different depths might lead, at least in the case of some organs,
to very interesting results.

_ As the rich material collected during the voyage of H.M.S. Challenger enabled me to
study the anatomy of at least some genera (Nymphon and Colossendeis), I eagerly made
use of this opportunity ; in the first place, in the hope of increasing our knowledge of the
morphological structure of the group, so that the question of their position in the zoological
system might perhaps be settled; and in the second place, to try in this way to illus-
trate the mode of life of those deep-sea animals which belong to our group.

My original intention of going through the whole anatomy of the Pyenogonids I have
given up, seeing that, however good the condition of the material might be, yet in regard
to some organs,— intestine, heart, &c.,—and for the histological structure of most organs, it
by no means takes the place of fresh material. Moreover, as I learned after a great part
of my anatomical researches was finished that Dr Dohrn’s Monograph is forthcoming, I
determined to limit the publication of my researches to those organs which had suffered
least from having been in alcohol for so many years. These are the integument, with
its glands; the nervous system, with the sensory organs; and the reproductive organs.
In regard to the intestine, the heart, &c., only some incidental observations were made,
which, in so far as they are thought important enough, will be recorded also.

1. Integument.—The integument of the Pyenogonids is only known from the publica-
tions of Zenker (1855),’ myself (1877),? and Dohrn (1879).? Zenker was the first to
observe the numerous cavities in the chitinous cuticle of Pycnogonum litorale. I,
however, had the good fortune to demonstrate that these cavities communicated by

1 Zenker.—Untersuchungen tiber die Pyenogoniden, Miiller’s Archiv, 1852.
2 Hoek.—Ueber Pycnogoniden, Niederlindisches Archiv fiir Zoologie, iii., 1877.
3 Dohrn.—Neue Untersuchungen tiber Pycnogoniden, Mitth. Zool. Stat. Neapel., i., 1879.

\ Ade
by +

REPORT ON THE PYCNOGONIDA. 101

means of very narrow canals with the exterior, and that they occur in all the genera of
Pyenogonids (at least in those I had then studied—Nymphon, Pallene, Phowichilidium,
and Pycnogonum). Moreover, I pointed out that as no respiratory organs are
present in the Pycnogonids, respiration must necessarily be integumentary ; it was my
conviction in 1877, as it is still, after a minute investigation of the Challenger material,
that the principal function of these canals is to serve for respiration. Contrary to
this opinion, Dohrn asserts that the cavities, with the pore-canals, which he says, were
rightly described by me, “zur Aufnahme von Hautdriisen dienen.” To settle this
question I investigated the structure of the integument of many species belonging to
different genera. I studied it in Nymphon hamatum, N. longicoxa, N. brachyrhynchus,
and NV. brevicaudatum; in Colossendeis leptorhynchus, C. gegas, and C. proboscidea ;
in Ascorhynchus glaber and A. orthorhynchus; in Pallene australiensis:; and in Phowi-
chilidium patagonicum, P. pilosum, and P. insigne.

Notwithstanding that my researches were especially directed to this point, I only
once succeeded in observing the glands referred to by Dohrn, and although I grant it is
possible that in some cases this may be owing to the condition of the animals, yet I feel
sure that as a rule these glands are not present.

A short description of the integument may find a place here. It always consists
of a subcuticular layer (epithelium), and of the chitinous cuticle. The subcuticular
epithelium is of a protoplasmic nature, with nuclei imbedded in it! (Pl. XVI. figs. 1 and
17, f); the chitinous cuticle in the different species shows a very different thickness,
and always presents a stratified appearance. It is never calcified, and, as a rule, is
coloured yellow by picrocarmine. Often, however, it shows two distinct lamin; an
internal very thick one, coloured violet by the picrocarmine, and consisting of numerous
alternately lighter and darker strata, and a comparatively thin external one, which
assumes a yellow colour when treated with picrocarmine (PI. XVI. fig. 1). To strengthen
the often extremely long and slender joints of the legs (especially the thighs and the two
tibial joints), the chitinous cuticle is often furnished internally with one (Ascorhynchus
glaber, Pl. XVI. fig. 9) or two (Nymphon hamatum, Phowichilidium insigne) longitudinal
ridges, which project into the interior of the leg. The form of these ridges on a transverse
section is by no means always the same, as may be seen from the figures 6, 9, 11, 16, 17,
and 18 on Pl. XVI. The septa of connective tissue, which in most genera divide the
cavity of the jomts of the leg (Colossendeis, e.g., fig. 16, Pl. XVI.), often have a point
of attachment in these ridges.

As a rule the chitinous cuticle of the Pyenogonids is perforated by two kinds
of cavities, the one of an irregular conical shape, terminating externally in a narrow
pore-canal; the other much narrower, and rather more cylindrically shaped, is filled

? The subcuticular epithelium of Pallene australiensis, Hoek, is richly furnished with a dark brown pigment. I
did not observe this in any of the other species.

102 THE VOYAGE OF H.M.S. CHALLENGER.

with a protoplasmic substance, often containing nuclei. No doubt it is the protoplasmic
epithelium which fills these latter canals. A nerve passes through them, and terminates
at the surface of the cuticle in what Dohrn (loc. cit., p. 38) calls a “ Borstenapparat.”
Dohrn never observed a single seta’ at the end of these canals; but always two or more
(sometimes even a rosette of eight or nine) together. This observation of Dohm’s
seems to be most accurate ; as a rule I found the integument of the species of Nymphon
furnished with forked sete (Pl. XVI. figs 1, 2, 4, 7), one of the sete being often split
again (fig. 3); that of Pallene australiensis shows also forked sete; the integument of
Ascorhynchus glaber is also furnished with double setz, which are here extremely small
and rudimentary. One of the species of Phowichilidium (P. patagonicwm) shows a
combination of four or five (Pl. XVI. fig. 17), while in another species (Phoxichilidium
pilosum) two combined setze are always observed.

In Colossendeis sete are totally wanting; and thus in this respect the genus
Ascorhynchus, with its rudimentary sete, stands between Nymphon and Colossendeis.

According to Dohrn,’ this pore-canal, which terminates in these forked sete, “ often”
takes its origin from one of the integumentary cavities, which he saw filled up with glands.
Dohrn therefore considers these sete as tactile organs, having probably the special
function of causing on irritation, by reflex action, the secretion of a poisonous fluid by
the glands, which are situated in the conical cavities of the integument. I think this
a very ingenious supposition, but I wish to state in opposition to it, that according to
what I have seen of the matter—(1) as a rule the cylindrical and narrow pore-canals do
not originate in the conical cavities ; and (2) that the occurrence of the glands in the
conical cavities is the exception, and that, as a rule, these cavities are empty or partly
filled up with a protoplasmic substance, nuclei, blood-corpuscles, &c. In the different
species of Nymphon it hardly ever happens that the pore-canal with the sete takes its
origin in a conical cavity ; in the species of Phoxichilidiwm it does not seem to be so rare
(Pl. XVI. fig. 17), even in these species, however, it is by no means the rule.

With regard to the form of the conical cavities, in the first place it must be men-
tioned, that they have a most regular conical shape in the different species of the
genus Nymphon, and also in some species of Pallene. In Phowichilidium they are of a
more elongated form, and often a small lateral branch passes from the main canal near
the extremity (Pl. XVI. fig. 17, 6). The genus Colossendeis shows these cavities of a
much more irregular shape. As a rule every cavity is bifid, and terminates in two
narrow pore-canals (Pl. XVI. fig. 12, c). The cavities are usually almost quite filled
up with protoplasmic substance. In this genus I once observed distinct cells, with large

1 Huxley calls “seta” all the hair-like processes from the fine microscopic down to stout spines, which are found
‘on the outer surface of the cuticle (Crayfish, London, 1880, p. 197). I use the word here, and on the following pages,
ina much more restricted sense; having already used the words hairs and spines for the integumentary appen-

dages, I call “ sete” those which I consider as being more particularly of a sensory nature.
2 Loc. cit., p. 38.

oe
eS

REPORT ON THE PYCNOGONIDA. 103

nuclei, in these cavities. This was in the first tibial joint of the leg of Colossendeis
leptorhynchus ; however, I think there can be no doubt that these same cells will also be
found in the other joints of the legs of this species. Each cell terminates in a long and
slender appendage, which probably extends to within a small space of the opening of the
canal. Most probably these are the glands which, according to Dohrn, are always present
in these integumentary cavities. I have figured these glands in fig. 1 of Plate XVIIL: dis a
part of the wall of the intestinal cecum, which runs through the joint ; ¢,¢ are parts of the
septa of connective tissue, which seem to form here separate chambers in connection with
the different cavities. These chambers contain numerous blood-corpuscles of an irregular
spool form, and towards the pore-canal are furnished with two (2), in an other cavity
three (d’) glandular cells, with very large nuclei. The specimen, the integument of
which shows these glands, is a female.

Returning to these integumentary cavities, and their ordinary, viz., their respiratory,
function, I have still to mention that I found them in many species with many blood-
corpuscles in their interior, and that often also a nerve is seen which sends a very thin
branch into them. These I observed more accurately in Colossendeis proboscidea, Sab.
(See later, under peripheral part of the nervous system.)

The number of these cavities is different in the different species. I counted them in
transverse sections of the fourth joint of the leg in some fourteen species, belonging to
five genera, and compared them with the girth of the joint. This I did to ascertain if
there was any relation between the number of these cavities and the depth at which the
species lives. That such a relation does not exist, and that the greater or smaller number
of these cavities is one of the properties of the natural groups (genera) of the Pycnogonids,
is shown, I believe, by the following table :-—

ee
————

Cites | mbes, ||
- 0 etitie umber

Name)ofither Species. is fourth Gone Ft Ap lieccand per millimeter. in Signe!

of the leg. F
section.

Nymphon brevicaudatum, Miers, . 3°25 5 1°54 73
Nymphon brachyrhynchus, Hoek, . 1°52 22 14-4 83
Nymphon robustum, Bell, . : 46 27 59 458
Nymphon longicoxa, Hoek, . 2°35 12 Dall 1100
Nymphon hamatum, Hoek, . : 3°47 37 10°7 1488
Ascorhynchus orthorhynchus, Hoek, 34 90 26°5 130
Ascorhynchus glaber, Hoek, . ‘ 3 56 18°6 1375
Colossendeis proboscidea, Sab. (sp.), 10:2 106 10 540
Colossendeis leptorhynchus, Hoek, 3°37 63 18-7 1126
Colossendeis brevipes, Hoek, . 3°15 62 20 2650
Pallene australiensis, Hoek, . 2°4 20 83 79
Phoxichilidium insigne, Hoek, 1:57 41 26 14
Phoxichilidium patagonicum, Hoek, 5:2 112 21°5 117
Phoxichilidium pilosum, Hoek, 417 45 10°8 1790

104 THE VOYAGE OF H.M.S8. CHALLENGER.

When comparing the number of these cavities in the fourth joint of the leg with that
of the same organs in a transverse section of the body,—for example, between two lateral
processes, where the circumference of the body is in some species nearly the same as that
of the fourth joint of the leg,—I observed almost the same number of cavities. This
was the case at least in Nymphon hamatum and in N. brachyrhynchus; whereas in
the other species more or less considerable differences were observed, the number of these
cavities in some species being greater in the legs; in others, on the contrary, round the
body.

With regard to the hairs and spines on the surface of the body, I have already pointed
out above that, as a rule, species occurring at great depths are rather smooth, whereas
those from shallow water are furnished with numerous hairs and spines. Thus Vymphon
longicoxa and N. hamatum have the surface almost quite destitute of spines; Nymphon
brevicaudatum and N. hirtipes occurring at moderate depths, the former not exceeding
120 fathoms, the latter never reaching 300 fathoms, and generally found in considerably
shallower water are the most hairy species of the genus. On the contrary, Nymphon
brachyrhynchus, occurring at depths not exceeding 120 fathoms, is almost as smooth
as Nymphon hamatum.

The species of Colossendezs, and especially the three more accurately studied by me,
show almost a perfectly smooth surface. The sensory setee are wanting also in these species ;
and the few spines which are present are very short and conical (Pl. XVI. fig. 13). Of
these three species, two are true deep-sea inhabitants; but the third (Colossendeis
proboscidea, Sab. (sp.), as a rule, is found at a depth not exceeding 200 fathoms. Of the
species of Ascorhynchus, the smooth A. glaber is found at a depth of 1375 fathoms ;
but the surface of Ascorhynchus orthorhynchus is also not very hairy, yet this species
occurs at a depth of only 130 fathoms.

The shallow water genera Achelia and Ammothea are extremely hairy, whereas in
the genus Phoxichilidiwm some of the deep-sea species (P. piloswm and P. mollissimum)
show a particularly hairy surface. Both the spines and the sete are in these species of
a very remarkable length. Finally, Pallene australiensis, occurring at a depth of 38 to
120 fathoms, shows again the smooth surface of a true deep-sea species.

The form of these spines is also very different, but I think it is not necessary to describe
them. In some species the spines are not smooth, but serrated ; as, e.g., in the case of
Nymphon brevicaudatum, Miers, and Pallene australiensis, Hoek (Pl. XI. figs. 6, 7) ; and as
spines having a very curious shape I have pointed out already those of the sixth joint of the
ovigerous leg of Nymphon longicoxa. No doubt, these must be of great use to the animal in
holding the egg-masses, and perhaps also in furnishing a good point for the young ones to
cling to. Particularly interesting are also the so-called denticulate spines in the four last
joints of the ovigerous legs of most species. I may refer to the descriptive part of this report
for an account of their extremely different forms, their numbers, and their arrangement.

REPORT ON THE PYCNOGONIDA. 105

Different as the forms of these spines may be, their minute structure is always the
same, and, I think, quite identical with that of any other spine. The cuticle is perforated
at the place where the spine is inserted, and a thin and flexible part of this cuticle keeps
the spine in its place; a socket is thus formed in which the spine easily moves. The
spine itself is, near its imsertion, cylindrical and hollow, and its cavity is entirely or
partly filled with a protoplasmic substance, which is in continuity with the epithelium
of the integument. Towards the extremity the spine is flattened, chitinous, and no
longer hollow; the exterior margin of this flattened part is serrated (Nymphon), or
provided with extremely small teeth (Colossendeis). Originally I considered these spines
as being of a sensory nature ; but afterwards, as I was convinced of their chitinous composi-
tion, I changed my opinion. However, as it is not difficult to trace a nerve, at least in
some of the more transparent species, penetrating these spines, they may still be considered
as, to a certain extent, organs of feeling. On the other hand there are, perhaps, far more
important functions to be fulfilled by the ovigerous legs with the aid of these denticulate
spines, viz., those of seizing the food, and, last, not least, of holding the animal of the
other sex during the act of copulation. In most species where denticulate spines occur
the four last joimts of the ovigerous legs often lie rolled up spirally, with the rows of
denticulate spines turned inwards. These joints if wound round one of the legs or any
other part of the body of the animal with which it copulates, would necessarily secure a
very strong adhesion in consequence of the rows of spines.

In close relation with the integument are the glands, which occur in different
appendages of the body.

1. The glands of the palpi. These I observed in Discoarachne brevipes, where they
occur in the third joint of the palpi, and probably their secretion is poured out through
a sieve-like perforated spot at the end of the second joint (Pl. VII. fig. 10). In the
palpus of Ascorhynchus such a gland is also present. It is situated in the fifth joint, and
has the form of a long sack, whose wall is lined by small and very numerous glandular
cells. It is attached to the wall of the jot of the palp by means of numerous threads
of connective tissue, and it opens towards its distal extremity by means of a rounded
pore. In Ascorhynchus orthorhynchus this pore is placed at the tip of a small conical
excrescence ; but in Ascorhynchus glaber I did not observe this knob. Probably the
same glands occur also in other genera—e.g., in Colossendeis—but I could not ascertain
their presence.’

2. The glands of the ovigerous legs. These I observed in Nymphon, but their minute
structure can only be studied in fresh specimens. They open into a small pore, not far
from the beginning of the fourth joint of the leg. Hach gland seems to consist of the

1 The glands of the palpi are mentioned in Dohrn’s paper of 1879. He says of the nerve of the palpus: “Er um-
fasst auf seinem Laufe ein sonderbares, bisher unbekannt gibliebenes Excretionsorgan” (loc. cit., p. 31).

(ZOOL. CHALL. EXP,—PART x.—1881.) K 14

106 THE VOYAGE OF H.M.S. CHALLENGER.

true glandular part and of a wider part, which acts probably as a receptaculum and opens
into the fine pore."

3. The glands in the fourth joint of the legs of the males. These I observed in the
following species :—Nymphon hamatum, Nymphon brachyrhynchus, Ascorhynchus glaber,
Colossendeis leptorhynchus, Colossendeis proboscidea, Colossendeis megalonyx, Oorhynchus
aucklandie, Phoxichilidium insigne, and Pallene australiensis. Whether or not they
occur in the thighs of the males of all the species I dare not assert. I can only say that
I did not find them in the thighs of the following species:—Nymphon robustum,
N. brevicaudatum, N. longicoxa, N. grossipes, and Colossendeis gracilis. This may,
however, be the consequence of these glandular masses being present only during a short
period of the year—for example, only in the breeding season.

These are the glands which were observed by Dohrn. According to him (loc. cit.,
p- 36) they occur only in the male sex, and are found in the fourth joint of the legs, viz.,
in those joints in which in the females the ovaries are most strongly developed. Dohrn,
moreover, tells us that these glands are extremely variable in their appearance ; while in
Ammothea they are furnished with a single duct only, in Phowichilus there are fifteen
smaller openings. Dohrn supposes that the function of these glands is to secrete a viscous
fluid, wherewith the males agglutinate the eggs which have been laid by the females,
and attach them to their ovigerous legs.

As to the function of these glands, I was unable to make any observations from the
material preserved in spirits and brought home by H.M.S. Challenger. With regard to
their structure the following may be stated:—The glands are always composed of a
skeleton of connective tissue, the meshes of which are or are not filled with nucleated
cells, which doubtless are the true glandular cells. When these glands have the meshes
filled up with the nucleated cells (Pl. XVI. figs. 5 and 10), the skeleton of con-
nective tissue is not easily discerned; while in those cases in which the meshes
are empty (Pl. XVI. fig. 15) the structure of the connective tissue is easily observed.
In the form of the glandular cells small differences were also observed. In Ascorhynchus
glaber, they are fusiform and pointed at both extremities; in Mymphon hamatum,
they are rounded, but in both cases distinct nuclei are present. A considerable
difference, moreover, is seen in the greater or less degree of concentration which
the glandular masses had undergone. In Nymphon hamatum and in Ascorhynchus
glaber the gland in the fourth joint (which, however, in the latter species is also
present in the fifth joint of the leg) forms only a single mass, which runs through
the whole joint and opens at the one side in a row of pores, each of which is placed at
the tip of a chimney-like process. As seen in fig. 6, the gland in Nymphon hamatum
almost extends on the one side of the leg, between the intestinal caecum and the

1 These glands are also observed by Dohrn ; he calls them “ ein zweites noch grésseres Excretions- (oder Driisen ?-)
Organ (Ibid.).

REPORT ON THE PYCNOGONIDA. 107

wall, from the one longitudinal ridge to the other; whereas in Ascorhynchus glaber
(fig. 9) the row of pores is placed almost exactly opposite to the single but very strong
ridge. :

In Pallene and Phowichilidiwm the structure and the position of the glands show
nothing particularly interesting. In Pallene there are many pores, in Phoxichilidium
msigne only a single pore at the end of the joint, placed at the tip of a conical
exerescence (Pl. XVI. fig. 18k). The structure of these glands in Colossendeis
is extremely interesting. In the three species of this genus in which I studied them,
Colossendeis leptorhynchus, Hoek, Colossendeis megalonyx, Hoek, and Colossendeis pro-
boscidea, Sab. (sp.), the gland consists of very numerous more or less isolated parts of
a rounded or more longitudinal shape, each of them opening separately by a distinct pore,
or (Colossendeis proboscidea) three or four opening together in a single pore. In fig. 14
on Pl. XVI. I figure a part of the integument of Colossendeis megalonyx magnified ;
in fig. 15 of the same plate a part of the integument of Colossendeis leptorhynchus is
shown. The glands seem to correspond with a wide vesicle (0), in the interior of which
@ narrow canal (p) les wound spirally ; this canal is easily traced till it opens at the
pore. Those conical cavities into which the glands are seen penetrating are much wider
than the others. For the structure of the gland itself the specimen of Colossendeis leptor-
hynchus which I investigated was not all I could have wished. Ona transverse section it
looks quite as if all the original glandular cells had dropped from the connective tissue,
this tissue itself being the only part that remained as an empty skeleton. Perhaps the
state of preservation is to a certain extent the cause of this. The male specimen of
Colossendeis proboscidea, in which also I studied these glands was in a much better
condition. Plate XVIII. fig. 2 shows the distribution of the glands (y) over nearly
half the inner circumference of the skin of the fourth joint. Moreover, in fig. 3 a small
part of this skin is figured more strongly magnified with the glands opening into one of the
pores. The gland itself (g) shows a dense ball of round and nucleated glandular cells. A
comparatively wide and very transparent canal extends from the gland to the interior of
one of the integumentary cavities (c), and a very narrow duct (d), which is irregularly
rolled up, runs through this wide canal till it reaches the pore at the end of the cavity.
When studying a part of the skin of the leg from the interior it is easily seen that three
or four of these glandular bodies send their ducts into the same integumentary cavity.
From the beautifully developed net-work of nerves and ganglionic plexuses, which extends
over the whole inner surface of the integument, distinct nerves are seen arising and
penetrating the cavities or innervating the glands.

Finally, I wish still to mention the curious manner in which these glands of the
fourth joint of the male open in Oorhynchus aucklandie, Hoek. A very long
cylindrical appendage is inserted on the fourth joint a little behind the middle. The
gland opens at the tip of this appendage by means of a very long duct, which shows

108 THE VOYAGE OF H.M.S. CHALLENGER.

a distinct swelling (a kind of receptaculum) near the beginning.’ About the structure
of the gland itself in this species I have no observations to communicate.

2. Nervous System.—Of the different systems of the Pycnogonida the one most
eagerly studied is, without doubt, the nervous system, and this is quite natural, because
it has been rightly considered, that if any system could be expected to shed light on
the affinities of the Pycnogonids with the other Arthropoda, it would be the nervous
system.

Among the more important papers on the subject, those of Zenker, Semper, Dohrn, and
myself may be mentioned. The way in which Zenker (loc. cit.) treats of the nervous
system of Nymphon is not a very happy one, as he describes and figures it as consist-
ing of a supra-cesophageal ganglion and four thoracic ganglia. The account given by
Semper?” of the nervous system of this genus is much more accurate. He tells us that in
Nymphon the supra-cesophageal ganglion innervates the mandibles and the eyes, and that
the first of the five thoracic ganglia furnishes nerves to the proboscis, to the palpi, and
to the ovigerous legs, while the four following ganglia give off nerves to the four legs.
The number of thoracic ganglia is, according to Semper, also five in Pallene and in Achelha,
on the contrary only four were observed by him in three species of Phowichilidium. In
my paper the optic nerves of Pycnogonwm are described, and the number of ganglia in
Nymphon is given as five, in Pycnogonum as four.’ We find in Dohrn’s latest paper (Joc.
cit., p. 87) a much more detailed description of the structure of this system. The supra-
cesophageal ganglion innervates the mandibles, and, moreover, gives off an azygous nerve,
which dorsally innervates the proboscis, and forms a ganglion at about one-third from
the extremity of the proboscis. The first thoracic ganglion gives off three pairs of nerves ;
the first pair arising from the ganglion a little outside and below the insertion of the
cireum-cesophageal commissures, innervates the lateral parts of the proboscis. Like
the azygous proboscideal nerve, they form ganglia at about one-third from the
extremity of the proboscis, and these three ganglia are connected by commissures, which
thus form a secondary cesophageal ring. The second pair innervates the so-called palpi; the
third arises from the ganglion laterally towards the posterior part, it innervates the ovigerous
legs. Moreover, Dohrn observed that this first thoracic ganglion not only in the genera
furnished with palpi and ovigerous legs, but also in those forms which have lost their
palpi and even in the females, which have lost also their ovigerous legs, consists of three
nuclei of “ fibrilliren Punktmasse,” each of which gives off the fibres for the nerves re-
spectively of the proboscis, palpi and ovigerous legs. In a young stage of the embryological
development, Dohrn made the observation that the first ganglion really consisted of two

1 Such a long appendage, at the tip of which the gland opens, occurs also in Ammothea (Dohrn, loc. cit., p. 36).

2 Semper (C.), Uber Pyenogoniden und ihre in Hydroiden schmarotzenden Larvenformen (Arbeiten a. d. Zool.-
Zoot. Institut in Wirzburg, i., 1874, p. 278).

3 Loc. cit., p. 249.

REPORT ON THE PYCNOGONIDA. 109

not quite separated pairs of ganglia. Finally, Dohrn states in the same paper that besides
the five (six) double ventral ganglia there are two others, which, however, in some
genera, totally disappear, and in other genera are preserved only in a rudimentary con-
dition. Accordingly, Dohrn observed immature stages of Phoxichilus, in which, behind
the sixth ventral ganglion, were present two distinctly separated, although much smaller,
pairs of long ovate ganglia. Of these the first pair gives off no nerve, and the second pair
the two nerves for the abdomen.

For my observations with regard to the nervous system of the Pycnogonids, I made
use of the following specimens from the material of the Challenger Expedition :—one of
Nymphon hamatum, one of Nymphon brachyrhynchus, two of Nymphon brevicaudatum,
Miers; numerous specimens of Nymphon robustum, Bell; one of Colossendeis leptor-
hynchus, one of Colossendeis megalonyx, and one of Colossendeis proboscidea, Sab. ;
finally, one of Phowichilidium pilosum. What I tried to ascertain in my investigations
was, in the first place, the innervation of the cephalic appendages and of the proboscis,
in the second place the structure of the first thoracic ganglion, in the third place
that of the last thoracic ganglion, and the presence or absence of the two rudimentary
abdominal ganglia. In how far I have been successful in this may be judged from the
following :—

The nervous system consists in all species of Pycnogonids of a supra-cesophageal
ganglion, an oesophageal commissure, and five (seldom four) thoracic ganglia. The
supra-cesophageal ganglion is situated in the cephalothoracic segment ; however, its place
varies greatly with the form of this segment, and therefore it even shows small differences
in the different species of one genus. The differences in the different genera are more
considerable. In the genus Nymphon it is, as a rule, placed towards the hinder
extremity of the cephalic part of the cephalothorax, below the oculiferous tubercle, and
above the insertion of the two ovigerous legs. In the genus Colossendeis this
ganglion is found nearly in the middle of the cephalic part of the cephalothoracic segment,
which part is usually separated (distinctly in Colossendeis leptorhynchus, e.g.) from the
remaining part of the segment by means of a constriction; the oculiferous tubercle
is here exactly above the ganglion. In Phowichilidiwm the ganglion is found also
above the insertion of the ovigerous legs; but the oculiferous tubercle is in most species
of this genus situated quite anteriorly, on that part of the cephalothoracic segment which
overhangs the proboscis. As a rule the shape of this ganglion is round (PI. XVIII.
fig. 6), but in Colossendeis the comparatively small ganglion is much broader than long
(Pl. XVIII. fig. 4). Whereas, in the other genera the two cesophageal commissures are
very short, run parallel to each other, and enclose a narrow canal through which only
the cesophagus passes (Pl. XVIII. fig. 11 C.), in Colossendets (I observed it in Colossendeis
leptorhynchus, Hoek, and in Colossendets proboscidea, Sab., sp.) this canal is very wide
(Pl. XVIII. fig. 4), the commissures which connect the supra-cesophageal ganglion with

110 THE VOYAGE OF H.M.S. CHALLENGER.

the first thoracic ganglion are very long, and through the wide canal formed by these
not only the intestine passes but also two large muscles (Pl. XVIII. fig. 7), which serve
for the movement of the proboscis, and run from the posterior margin of the proboscis to
the hinder part of the dorsal surface of the cephalic part of the cephalothorax. These
muscles are anteriorly narrow, and grow considerably broader towards their extremity,
so that their shape is rather triangular. The nerves which arise from the supra-
cesophageal ganglion are the same in Nymphon, Phowichilidiwm, and Colossendeis. To
the front three comparatively strong nerves are always present.' Of these, that nerve
which is placed in the middle takes its origin in the ventral surface of the ganglion,
a little behind the front margin. This middle nerve is the azygous proboscideal nerve.
It runs close to the dorsal surface of the proboscis, and gives off at rather irregular dis-
tances extremely small nerves, which innervate the integument. At a distance of about
one-fourth of the total length of the proboscis in Nymphon, and of about one-eighth of the
same length in Colossendeis, it enters the ganglion (Pl. XVIII. fig. 8), which, no doubt,
has already been observed by Dohrn. The two mandibular (antennary) nerves arise from
the front margin of the supra-cesophageal ganglion ; they are nearly (in Nymphon and in
Phoxichilidium) of the same strength as the azygous proboscideal nerve. First they are
slightly divergent, then they approach each other again so as almost to touch the azygous
proboscideal nerve, then they separate again and direct themselves forwards and a little
upwards, running in the mandibles very close to that part of the dorsal surface which is
nearest to the mandible of the other side (Pl. XVII. fig. 4, n.m.). In regard to the
farther course of the mandibular nerve I could only observe that it divides into two
branches. These nerves are not totally wanting in the genus Colossendeis, and con-
sidering the case of Colossendeis gracilis with its distinct mandibles, we need not
wonder at this. Yet the nerves are very short and represented only by rudimentary
branches (Pl. XVIII. fig. 4, m). (Those of the interesting specimen of Colossendeis
gracilis | was unable to observe without dissecting the specimen.)

With regard to the innervation of thee yes, I observed distinct nerves arising from the
supra-cesophageal ganglion. These I have described already in my paper on Pycnogonids,
published in 1877, and their presence is confirmed by Dohrn’s observations. Dohrn (loc.
cit., p. 37) says that they arise from the sides of the ganglion, and that they are widely
separated from one another. Moreover, Dohrn tells us that there are two of them, and
that they divide and innervate the eye in a peculiar way. I studied the innervation of
the eyes in Nymphon brachyrhynchus, N. strémii, N. robustum, and in Colossendeis
proboscidea. The latter species is a blind one ; its eyes are represented only by a small

1 In the figure I give of the nerves arising from the supra-cesophageal ganglion of N. robustwm (Pl. XVII. fig. 4),
besides these three nerves two thinner ones are figured, These, however, are not present, as I ascertained after the plate
was printed off. Although I have given myself much trouble in trying to determine what it was I had mistaken for
nerves, I have not succeeded. The thin threads have the appearance of narrow ducts; they extend backwards to
behind the supracesophageal ganglion and pass between this ganglion and the upper surface of the cesophagus.

REPORT ON THE PYCNOGONIDA. iba

rounded spot distinguishable by its transparency. The optic nerves are represented by
two strong bundles of nerves, arising as in Colossendeis megalonyx (Pl. XVIII. fig. 4, 0)
laterally from the dorsal anterior surface of the ganglion. These nerves divide into
stronger and feebler branches, and the latter have small ganglia between them. Such
small ganglia are present also on the interior surface of the small transparent spot
representing the rudimentary eye. They are in relation partly with the nerve fibres
of the so-called optic nerve, partly with the complicated system of nerves and ganglia,
which covers in this species as in the other species of the same genus, the internal
surface of the integument. In this species of the genus Colossendeis, and from what I
have seen of the matter, the same is the case in Colossendeis leptorhynchus and C.
megalonyx, the optic nerve-bundles are really integumentary nerves, giving off the
nerve-branches, which, as will be shown hereafter, extend all over the inner surface of
the integument, having everywhere ganglia between them, and, as a rule, at small dis-
tances from one another.

I feel inclined to consider the condition of the eye, and of its innervation as described
for Colossendeis proboscidea, as the original condition in the Pyenogonida. As an
example of the most highly developed condition, I wish to describe that of Nymphon
brachyrhynchus. Dorsally the supra-cesophageal ganglion gives off two nerves, which
are at their origin quite covered over by ganglion cells (Pl. XVIII. fig. 11 C. 0’).
Where they arise from the ganglion, the distance between the two nerve-bundles is not
very considerable; they diverge slightly till they reach the base of the oculiferous
tubercle. Here each of these nerve-bundles divides into two branches which run
horizontally, the one towards that part of the integument which is before, the other
towards that behind the oculiferous tubercle. On reaching the integument each of these
two branches divides into numerous smaller nerves and nerve-fibres ; moreover, they
send upwards numerous nerve-fibres, which penetrate the oculiferous tubercle and extend
till they reach the outer wall of the eye. There can be no doubt, therefore, that the eye
is innervated by nerve-fibres not united together so as to form a distinct optic nerve.

The same mode of innervating the eye I observed in Nymphon strémii.. For the
study of the innervation of the rudimentary eye of Nymphon robustum 1 got good pre-
parations also. A part of one of these is figured in Plate XVIII. fig. 5. We have the
same nerve-bundles covered by ganglionic cells ; they do not, however, divide immediately
into the stronger integumentary and smaller optic nerves, but before doing so they enter
a comparatively large ganglion (fig. 5, g) from which these nerves are seen arising.
This same ganglion gives off also the nerves for the sete, which in this species are
present in considerable number at the tip of the oculiferous tubercle.

1 This quite corresponds with Dohrn’s observations, that the optic nerves give off also branches to the curious

organs observed by him between the eyes. I believe these organs are rudimentary in Nymphon, in Colossendeis proboscidea
they are totally wanting.

112 THE VOYAGE OF H.M.S. CHALLENGER.

While the eye of Colossendeis proboscidea, Sab., must probably be considered as
the most primitive condition, that of Nymphon robustum is undoubtedly a degenerated
form. In the innervation of the different stages of development of the eye of the
Pyenogonids I believe I have peinted out one common feature, viz., that the two
nerves arising from the supra-cesophageal ganglion may be only partly considered
as optic nerves, and that it is much more in accordance with the facts to call
them integumentary nerves, branches of which have assumed the function of optic
nerves. For the investigation of the development of the organs of sense and especially
of the eyes, I believe the study of the Pycnogonida will yield in future very interesting
results.

The number of thoracic ganglia in Nymphon, Colossendeis, and Phoxichilidium
pilosum is five. Those of Colossendeis (C. proboscidea, Sab., sp.) are figured in
Plate XVII. fig. 2; those of Nymphon robustum, Bell, in fig. 3 on the same plate.
In these three species the first ganglion (better called the first ganglionic mass) is
separated from the second by two distinct commissures, and in Nymphon robustum
and Phowichilidiwm pilosum even the outward form of the ganglion shows its complex
nature; on a longitudinal section it is seen to be composed of two distinct ganglia.
This anterior ganglionic mass supplies the two ventral parts of the proboscis, the
palpi, and the ovigerous legs; three pairs of strong nerves are given off by the
ganglion, which, judging from its anatomical structure and from its development (vide
Dohrn, loc. cit., p. 34, and also in this report swb embryology, with Pl. XIX. figs. 11 and
13) is composed of only two pairs of original ganglia." For a long time I was greatly
puzzled with this fact, until the study of the nervous system of Colossendeis dispelled
my doubts.

In fig. 4 of Plate XVIII. I figure the supra-cesophageal and first thoracic ganglia
of Colossendeis megalonyx. The latter gives off the two nerves for the ovigerous legs
(0), the nerves for the palpi (pa), which in the same way as the nerves for the
lees immediately divide into two branches, and in the third place the two nerves for the
proboscis (¢’”). Moreover, a fourth nerve (¢’) is observed, which serves also for the
innervation of the proboscis, and the fibres of which arise from the same part of the
ganglion as those of the main proboscideal nerve. For a short way these fibres run
parallel with the fibres of the commissures, so that this first pair of proboscideal
nerves seems to arise from these commissures.” These same nerves are also present in

1 On page 32 of the same paper, Dohrn asserts that in the first thoracic ganglion three nuclei are present of the
well-known “fibrillaren Punktmasse.” This does not agree with what I have seen in the three genera I studied, nor
does it agree, I believe, with what Dohrn himself says on page 34.

2 Tn fig. 2 on Plate XVII. the ventral part of the nervous system of Colossendeis proboscidea, Sab., sp., is figured,
From the first thoracic ganglion arise the nerves for the ovigerous legs (n. o. I.), and a strong nerve (the palpus nerve)
dividing into two branches (n. pr. and n. p.) The most anterior, and at the same time most dorsal, part of this ganglion,

from which arise the two pairs of proboscideal nerves, and the commissures, has not been figured, having been removed
during the preparation.

REPORT ON THE PYCNOGONIDA. 113

Nymphon in a much more rudimentary state. Nobody would conclude, however, from
their presence that the first ganglion was originally composed of four ganglia; but the
supposition of its being formed of three nuclei loses at the same time much of its value,
and the ventral part of the proboscis must be considered as being innervated by the same
original ganglion as that which gives off the nerves for the palpi.

I believe there can be no doubt that we have here the original condition of the
nervous system ; at the same time this fact may be considered as suggesting the opinion
that the palpi originally belonged to a pair of appendages which coalesced to form the
two undermost of the three parts of which the proboscis is composed.

The two front nerves of the first thoracic ganglion in Nymphon and Phoaichilidium,
and the strongest of the two front nerves of the same ganglion in Colossendeis,
enter the proboscis and run forwards exactly in the middle of the two ventral parts
of the proboscis, which I compared (note on p. 14) with the carpels of a monocoty-
ledonous fruit. These nerves I call the paired proboscideal nerves. They end, like the
azygous proboscideal nerve, by entering a ganglion, placed at about the same distance
from the end of the proboscis as the ganglion of the azygous proboscideal nerve. These
three ganglia are united by a ring, which runs between the outer wall of the proboscis
and the chitinous wall of the cesophagus, among the numerous muscles which run from
the one wall to the other.

So far my description quite agrees with that of Dohrn, as given above. However, a
considerable difference arises from the fact that the ganglia which weré seen by Dohrn
are not to be considered as ganglia of the azygous or paired proboscideal nerves, but
as being really the terminal ganglia of three strong nerve bundles, composed of nerve
fibres and ganglia, which run longitudinally below or above the three stout proboscideal
nerves, so that they lie between these nerves and the wall of the cesophagus. The
discovery of these three ganglionic nerve bundles has been very fortunate. It is curious
that they have hitherto been always overlooked, and especially that Dohrn did not
observe them. But then it must be considered that these nerve bundles are placed
among numerous muscles running over and beneath them, and making a preparation
totally impossible. A successful longitudinal section, made exactly above or below a
bundle, is the only way to detect it. I call these bundles ganglionic, for although
I do not believe that their function is analogous with that of the sympathetic system
of higher animals, yet their structure shows in general the same relative distribution
of ganglion cells and nerve fibres as in the case of the ganglionic system of higher
animals.

Fig. 6 on Plate XVIII. shows the position of these nerves in the proboscis; while
fig. 8 shows a part of one of them more strongly magnified. Each of them (g) consists
of a strong bundle of nerve fibres, which, posteriorly at irregular, anteriorly at more

regular distances, are surrounded by groups of ganglion cells. Thus each of the
(ZOOL, CHALL. EXP.—PART x.—1881.) K 15

114 THE VOYAGE OF H.M.S. CHALLENGER.

cords has the appearance of a row of ganglia connected by bundles of nerve fibres.
The size of these ganglia is not quite the same over the whole cord, the foremost beg
slightly larger than those placed more posteriorly. As to their shape, I observed the
following two different types. In some of the ganglia the cells are placed on both
sides of the bundle, which passes through it, and these ganglia have a very regular
rhomboidal form. The other type is represented by those ganglia in which ganglion
cells are to be observed only on one side of the nerve bundle, and which accordingly
show a triangular form. The triangular ganglia seem to be more numerous in
Colossendeis, the rhomboidal form in Nymphon; in both genera, however, the stout
ganglia, which are placed in the front part of the cord, and in the first place the
comparatively large ganglion (figs. 6 and 8 y) observed by Dohrn are of a distinct rhom-
boidal form.

The form of the ganglion is, of course, determined by the number of nerves which
branch off from it. The different ganglia give off besides numerous smaller nerves,
one (in the triangular form) or two (in the rhomboidal) stouter nerves. These run in
the foremost part from the one ganglionic bundle to the two others, and form nerve-
rings (fig. 6, at a a™ &.), of which the secondary cesophageal ring (figs. 6 and 8 a)
observed by Dohrn is the first and the stoutest. In Nymphon robustum 1 observed
five or six of these nerve rings, but in Colossendeis they are still more numerous.

With regard to the three stout proboscideal nerves, which have been observed already
by Semper and Dohrn, and which, according to the latter author, terminate in the three
ganglia (the front ganglia of my ganglionic bundles), I have ascertained that they are
connected with the ganglionic bundles in the following way :—They run superiorly to and
quite independently of the ganglionic bundle, till they reach the last but one ganglion of
that bundle (fig. 8 wv). This they enter, their fibres passing through it and contributing to
the comparative thickness of that part of the bundle which unites the last but one and
the last of the ganglia (fig. 8 y). However, it is very probable that at least some of these
fibres extend beyond the last of the ganglia. I am not quite certain whether perhaps,
a union of the ganglionic cord with the proboscideal nerves does not also take place
posteriorly. As I have stated already above, the proboscideal nerve gives off branches ;
and about the middle of the proboscis of Colossendeis proboscidea, Sab. (sp.), on both sides
of the stouter middle nerve two thinner cords run parallel with it in its immediate neigh-
bourhood ; these are branches of the middle nerve. Investigating the first part of these
lateral branches, close to their origin from the main proboscideal nerve, I once observed
(in Colossendeis megalonyx, Hoek) very small ganglia with thin nerve threads running
along this nerve without, however, exchanging fibres; these are, possibly, the end
branches of the ganglionic bundle. While the origin of these branches and their
connection with the proboscideal nerves is so easily noticed, with regard to their
termination I only observed that the bundles, when approaching the end of the proboscis,

REPORT ON THE PYCNOGONIDA. i15

become thinner and thinner, the ganglia smaller, and the lateral branches arising from
the ganglia more numerous and much thinner and shorter. This is quite in correspond-
ence with the number of muscles which these ganglia innervate ; whereas these in the
front part of the proboscis are stouter and separated by distinct longitudinal intervals,
in the posterior part they are thinner and placed almost in an uninterrupted row.

This brings us quite methodically to the function of these ganglionic nerve-bundles.
In the vertebrates we can distinguish by the microscopical structure sympathetic ganglia
and nerves from those of the cerebro-spinal system, but in the invertebrata this is by
no means so easy. In the first place, we must consider the function of the part of the
nervous system in question. The ganglia and the nerves of my three ganglionic
bundles innervate the striped muscles of the proboscis. Unstriped muscular fibres
are by no means rare in the muscular tissue of the Pyenogonids,' but even if they
were quite wanting, as they seem to be in the muscular tissue of the Crayfish, those of
the proboscis ought to be considered as voluntary fibres. Moreover, the action which
the food undergoes in the proboscis by means of these fibres is of a purely mechanical
nature, Chemical action does not take place in it, therefore comparison of these
ganglionic bundles with the sympathetic system of higher animals is impossible.

The morphological explanation of their presence is by no means go easily given. The
following reasoning must be considered as an attempt only. The proboscis of the Pyeno-
gonida in the form in which it presents itself should not, of course, be considered as a new
organ, only present in this class of Arthropoda. It is only an organ or a combination of
organs under a new form, modified under the influence of surrounding conditions. Con-
sidering for a moment the supposition right, that it results from the union of three parts,
an azygous one placed partly above and partly before the mouth (the upper lip),
and two others placed below and behind the mouth, the mandueating parts of the
mandibles, of which the palpi in that case may be considered as the feelers ; then we
have in the three nerves, the first of which is given off by the Supra-cesophageal ganglion,
and the two others arising from the first thoracic ganglion, the normal nerves for the
innervation of these parts. With the union of these parts to form a proboscis (and I
believe this argument will hold good also if we prefer another homology for these parts),
and the predominance of the mandueating function of this proboscis, evidently quite a
new part of the nervous system, will make its appearance; and it is not difficult to
imagine its probable origin.

In the chitinous wall which lines the canal of the proboscis, and which is furnished
with rows of very numerous teeth and spines, we have, no doubt (morphologically), acon-
tinuation of the integument, so that its inner surface corresponds with the outer surface of
the body, while its outer surface, to which the muscles are attached, is the homologue

1 E.g., in the wall of the vasa efferentia of the males, &e. ; * Huxley, The Crayfish, p. 181.

116 THE VOYAGE OF H.M.S. CHALLENGER.

of the inner surface of the skin. Now, this inner surface of the integument both of the
body and the legs, especially in species of the genus Colossendeis, is richly furnished with
ganglia, which spread all over it and are connected with nerves. They are so very
numerous as to form a continuous network of ganglia and nerves, their function being,
I believe, to innervate the cavities of the integument, for which I have suggested a
respiratory function. There can therefore be no difficulty in supposing that the ganglia
of my ganglionic bundles are derived from originally integumentary ganglia, and that
their high development is to be attributed to the changed functions of the parts which
surround the mouth.

While these same ganglionic bundles, in a more or less developed state, are found
in all species and genera of Pyenogonida, it is very probable, I believe, that in the other
classes of the Arthropoda their homologues will be sought for in vain. The shape of the
terminal ganglia, of which the dorsal one is the largest, is best seen from the drawing
(Pl. XVIIL. fig. 8). Of the nerves which arise from it, two run in an oblique direction
(one to each side), these enter again (at least in Nymphon) a small ganglion, from which
nerves are given off to the tactile organs placed in the so-called lips of the proboscis.
Of these small ganglia, those two, which are placed on both sides of one of the lines of
union of the three proboscideal parts, are again connected by means of a nerve string.
The tactile organs consist of a small tuft of hairs placed just at the end of the chitinous
list which marks the place of union of two of the proboscideal parts meeting there
laterally. Perhaps the nerve fibres of the small nerve bundles, which enter the secondary
ganglia and innervate these tactile hair-tufts, take their origin in the three original
proboscideal nerves.

Besides the three original nerves and the three ganglionic bundles, two thinner
nerves enter the proboscis dorsally. These I observed only in Nymphon arising from
the supra-cesophageal ganglion. The two thin nerves which in Colossendezs run along-
side and quite near to the main proboscideal nerve must be considered as branches of
this main nerve, and no doubt there are still other longitudinal nerves, which run
through the proboscis, and which must also be considered as branches of one of the three
main nerves.

What I observed in regard to the remaining part of the nervous system is the
following :—The shape of the four thoracic ganglia may be seen from the figures on
Plate XVII. The length of the commissures uniting these ganglia is different in
different genera, and even in the different species of one genus. In Nymphon robustum,

1 It seems to me that an analogous case is that of the visceral or stomatogastric nerves of the Crayfish, studied by
differeut authors, and investigated recently more accurately by Prof. Huxley (Anatomy of Invertebrated Animals,
London, 1877, p. 330), a complex nervous apparatus, serving chiefly for the innervation of the muscles of the mandibles,
and for that part of the intestine which has been called by Huxley the gastric mill. This gastric mill of the Decapod
Crustacea is placed behind the esophageal commissures ; the analogous apparatus of the Pycnogonids is found in front
of the same commissures.

REPORT ON THE PYCNOGONIDA. Utlys

Bell, e.g., the commissures between the third and fourth ganglia are the longest; in
Nymphon brachyrhynchus, however, those between the second and third are the longest.
In Colossendets and in Phoxichilidium pilosum the relative length is the same as in
Nymphon robustum. Tn all the species and genera I observed the commissures between
the last two thoracic ganglia to be shorter, often much shorter, than those between the
preceding ganglia. The nerves which arise from these ganglia in Colossendeis immediately
divide into two branches, whereas in Nymphon they only separate after having reached
the middle of the lateral process at the end of which the leg isinserted. In Phowi-
chilidium pilosum they again divide immediately after leaving the ganglion. The last
ganglion has a truncated form; in most of the genera I studied I observed at least a
trace of the presence of the small accessory ganglia (abdominal ganglia) which Dohrn
observed in Phowichilus, and which I found beautifully developed in a young specimen
of Colossendeis proboscidea.

Close to the hinder margin of the ganglion two small excrescences arise from its
dorsal surface. They are separated from one another by a small space, and as they unite
again at a short distance from the ganglion a round area is left between them. Ina
full-grown specimen of the same species only a single excrescence was observed, arising
from the hinder margin, and I observed it of the same form in Colossendeis megalonyx
and also in C. leptorhynchus. I did not observe it in Nymphon; but in the species
of that genus which I studied (N. strémii and N. robustwm) I always saw two distinct
medullary nuclei in the interior of the ganglion placed close to its hinder margin, behind
the large medullary masses from which the nerves for the hindmost pair of legs arise.

According to Dohrn, the nerves which arise from this ganglion are two in number,
besides the two stout nerves for the hindmost pair of legs. It is extremely difficult to
avoid confounding threads of connective tissue, arising from the neurilemma that surrounds
this ganglion with nerves. I have, however, distinctly observed that often four different
nerves branch off from the ganglion ; in Colossendeis proboscidea, e.g., two smaller ones
are given off more in the middle from the dorsal excrescence, and two stouter ones
leave the ganglion nearer to the nerves which innervate the fourth pair of legs. Two
pairs of nerves arising from the hinder surface are also present in C. leptorhynchus; but,
strange enough, only one pair (that arising from the excrescence in the middle of the
hinder margin) in Colossendeis megalonyx. In the genus Nymphon the two nerves which
arise from the ganglion leave it as one single nerve, and only afterwards divide into two
branches. The same difficulty is experienced in ascertaining the presence of nerves
branching from the commissures which unite the different thoracic ganglia. These are
present, however, in all the genera, and even in all the species I studied. As a rule, they
leave the commissures much nearer to the preceding than to the following ganglion, but
often also nearly in the middle of the commissures; between the second and third,
between the third and fourth, and between the fourth and fifth thoracic ganglion,

118 THE VOYAGE OF H.M.S. CHALLENGER.

distinct nerves are observed arising at an acute angle from the commissures. These
innervate the muscles which run from the one segment to the following one.

I give a figure (Plate XVIII. fig. 10) of one of the small ganglia and the nerve
fibres arising from it on the inner surface of the integument, I observed these ganglia
in Nymphon and in Colossendeis; they are more numerous in the latter genus, and
especially numerous and in a better state of preservation in one of the specimens of
Colossendeis proboscidea, Sab., dredged last summer north of Scotland. The figure is
taken from a part of the integument of a specimen of this species.

To show the minute structure of the ganglia I give in fig. 11 A—F a series of six figures
illustrating vertical (frontal) sections through the supra-cesophageal and first thoracic
ganglia. As will be easily seen, the sections do not form a complete series, they are only
the most interesting out of a series of about twenty. Fig. A represents a section
quite at the front of the supra-cesophageal ganglion ; a distinct and comparatively thick
neurilemma sheath surrounds the whole ganglion, and three distinct medullary nuclei
(pointed substance according to Leydig) show the place of origin of the three main
nerves. The rest of the section is composed of ganglion cells, with the exception of a
small medullary spot at the left side, which does not occur at the other side,
and proves that the section is somewhat oblique. Neither the cesophageal com-
missures nor the first thoracic ganglion are yet to be seen in this section, Fig.
B represents a section which passes through the supra-cesophageal ganglion and
through the foremost part of the first thoracic ganglion, but not yet through the
commissures. Almost the whole section is occupied by the medulla, which forms
regular prominences towards the periphery, and only a very small space is occupied by
the ganglion cells; m is the lobe for the mandibular (antennary) nerve, 0 represents the
lobe for the optic nerve, and z is a median lobe about the function of which I do not feel
quite sure. In section C this median lobe is no longer to be observed, and the optic
lobes have here assumed a much more elongated form. In section B the commissures
are still totally wanting, but the front part of the first thoracic ganglion, with the
medullary nuclei (p) for the two infra-proboscideal nerves, are distinct. These in
section C are reduced to small lobes, while those for the nerves of the ovigerous legs (¢)
are distinct. In this section the cesophageal commissures are seen, and also the under-
most parts of the two optic nerves, which arise from the supra-cesophageal ganglion
(o’). Their connection with the optic lobes, however, does not occur in this section.
Section C passes almost through the middle of the oculiferous tubercle, so that two eyes
are placed in front of this section and the two others behind it. Section D represents the
last part of the supra-cesophageal ganglion ; the hindmost part of the medulla is seen, and
the ganglion cells begin again to increase in number. Of the first thoracic ganglion, the
section goes through that part of the medullary centrum which gives off the nerves for
the ovigerous legs (7). In E this medullary centrum is considerably less voluminous, and,

REPORT ON THE. PYCNOGONIDA. 119

finally, in F only two rounded spots of medulla are left (co’), which give off the com-
missures between this and the second thoracic ganglion.

About the histological structure of the ganglia I wish to be very short. In fig. 12 on
Plate XVII. a longitudinal section is given of the first thoracic ganglion of Mymphon
brachyrhynchus. A comparatively thick sheet of connective tissue (neurilemma sheath)
surrounds the ganglion, and is in continuation with the sheath of the commissure which
unites this ganglion with the second thoracic ganglion. Small ganglion cells, each
with a distinct nucleus, fill that part of the ganglion which is not occupied by the nerve
fibres. These ganglion cells are situated in meshes of connective tissue, they are small
and furnished with but little protoplasm ; their nuclei are distinct, and show a small and
glittering nucleolus.

In a section through the first thoracic ganglion of Colossendeis leptorhynchus,
it is easily observed, that the ganglion cells are of two different sizes: there are
very large ones rich in protoplasm, and furnished with comparatively large nuclei;
there are also very small ones, which show only a small quantity of protoplasm. Fibres
and sheets of connective tissue are everywhere observed between the ganglion cells; the
neurilemma sheath of the ganglion itself is very thick, whether it is to be considered
as really double (an outer and an inner neurilemma sheath, the latter of which should bein
connection with the connective tissue meshwork of the interior of the ganglion), I have
not been able to ascertain.?

3. Eyes.—Of the organs of sense I paid special attention to the eyes. Besides the
tactile organs spread over the whole surface of the body, the curiously shaped hairs of the
palpi of Ascorhynchus, and perhaps of other genera, which probably are also organs of a
special sense (olfactory ?), the eyes are the only certainly known organs of sense in
Pyegnogonids.’? In the first place, I tried to ascertain in how far the eyes can really be
said to disappear in those animals which inhabit great depths. I therefore drew up the
following list, in which the species from the “Challenger” and “ Knight Errant” expedi-
tions are placed according to the depths they inhabit.

1 Hitherto I have studied only such sections of the ganglia as are made by cutting the whole body. These are
sufficient for researches on the general anatomy, but totally insufficient with regard to histology. The numerous sheets
and strips of connective tissue prevent the substance used for enclosing the body (paraffine or Calberla’s substance) from
penetrating the whole interior of the body. Thus some parts always remain disunited, and the cutting of thin sections
is extremely difficult, if not impossible.

2 The curious organ which Dohrn observed between the two eyes on each side of the oculiferous tubercle I have
not observed. Perhaps it does not occur in Nymphon, the only genus in which I investigated the eyes.

120

Name of Species.

Discoarachne brevipes, Hoek, .
Hannonia typica, Hoek, 5
Phoxichilidium fluminense, Kroyer,
Phosichilidiwm insigne, Hoek,

Nymphon brachyrhynchus, Hoek,
Nymphon brevicaudatum, Miers,

Nymphon fuscum, Hoek,

Ascorhynchus minutus, Hoek,
Pallene languida, Hoek, .

Pallene levis, Hoek,

Pallene australiensis, Hoek, . ‘

Phoxichilidium patagonicum, Hoek,

Pycnogonum litorale, Strom, .
Colossendeis megalonyx, Hoek, .
Nymphon grossipes, Oth. Fabr., sp.,
Nymphon brevicollum, Hoek, . :

Colossendeis robusta, Hoek,

Ascorhynchus orthorhynchus, Hoek,
Nymphon robustum, Bell, :
Colossendeis leptorhynchus, Hoek,

Nymphon strom, Kroyer, . .

Nymphon macronyx, G. O. Sars,
Colossendeis proboscidea, Sab. (sp.), +
Phowichilidium patagonicum,

var. elegans,
Oorhynchus awucklandie, Hoek,
Nymphon perlucidum, Hoek, . °
Nymphon longicoxa, Hoek,
Nymphon compactum, Hoek, .

Colossendeis minuta, Hoek, . .

Ascorhynchus glaber, Hoek, .

THE VOYAGE OF H.M.S. CHALLENGER.

Depth

in
Fathoms,

7-20
7-20

10-120
25-125

25

38
38
38-40
38-120
45-120

53
55-120
83-540

83

120

150
375-540
400-1600
515-540

540
540

600

700
825
1100
1100
1250

1375

Condition of the Eyes.

Small; placed on a blunt tubercle.

Small; placed on a rounded tubercle.

Two anterior a little larger than
the two posterior.

Size of the eyes different, as in the
foregoing.

Large ; oculiferous tubercle pointed.

Small ; oculiferous tubercle ex-
tremely elevated.

Small; touching one another at
the tip of a not very prominent
tubercle.

Small; oculiferous tubercle not
very prominent.

Middle-sized; tubercle blunt and
low.

Middle-sized ; tubercle acute.

Two anterior large, the two pos-
terior much smaller. Tubercle
high, but blunt.

Extremely small; tubercle blunt.

Two anterior a little larger than
the two posterior. Tubercle ele-
vated.

Large; placed at the base ofa high

and acute oculiferous tubercle.

Large; oculiferous tubercle low.

Two anterior large, two posterior
small; oculiferous tubercle ele-
vated and acute.

Middle-sized, with pigment ; oculi-
ferous tubercle acutely pointed.

No lens, and no pigment.

Two small spots (rudimentary
lenses?) at both sides of the
blunt tubercle.

Two larger ones directed forward,
two smaller ones backward.
Tubercle blunt.

Not very large; tubercle bifid at
the extremity.

Two small spots (rudimentary
lenses?) on both sides of the
oculiferous tubercle.

Two large eyes directed forward,
two smaller ones directed back-
ward. Tubercle high, acute.

Small, with pigment; tubercle
directed forwards.

Small; the pigment light-brown-
ish; tubercle lowand blunt.

Observations.

Ablunt oculiferous tubercle,
without eyes or pigment.

Form of the tubercle differs
with age.

Form of the tubercle differs
with age.

Oculiferous tubercle ob-

liquely truncated.

Younger specimens with a
more elevated tubercle.

Tubercle of the younger
specimens elevated,

Oculiferous tubercle low,
without pigment.

Oculiferous tubercle repre-
sented by a round spot.
Two small rudimentary
spots, without pigment;

tubercle blunt.
Oculiferous tubercle elevated.

REPORT ON THE PYCNOGONIDA. 121

nT a A
Depth Number,

Name of Species. in -
Fathoms, of Eyes.

Condition of the Eyes. Observations.

| Nymphon hamatum, Hoek, . - | 1375-1600 Soc aes Oculiferous tubercle also
we rudimentary.
Colossendeis gigas, Hoek, . b . | 1875-1600 oa ore Oculiferous tubercle of the

youngerspecimens higher,
and furnished with two
rudimentary spots.
Colossendeis gracilis, Hoek, . . | 1375-1600 =a Oo, Oculiferous tubercle much
; ; elevated, with four lenses.
Phoxichilidium pilosum, Hoek, . | 1600-1950 | Four, | Two large ones directed forward,
two very small ones backward;
: tubercle elevated and acute.
Nymphon meridionale, Hoek, . len LGD) - Distinctly pigmented ; tubercle not

k very high.
Phowichilidium oscitans, Hoek, : 1675 5 Two very large ones and two small
. : ones.
Phoaichilidium mollissimum, Hoek, 1875 5 Two extremely large ones, kidney-

shaped, directed forward; two

very small ones directed back-

ward.
Nymphon procerum, Hoek, . 5 2160 doc : 600 ‘Two small spots are present

; on the tip of a low
ee : tubercle.
Nymphon longicollum, Hoek, . 5 2225 ane me - | Oculiferous tubercle high,
NA with two rudimentary
: spots without pigment.
Colossendéis media, Hoek, - . : 2225 Boo ee Oculiferous tubercle very
high and acute.
Colossendeis brevipes, Hoek, . : 2650 aes op Oculiferous tubercle high
: and acutely pointed.

What we learn from this list is that it is a common feature for the shallow-water
species to have four distinct eyes ; and for those inhabiting a depth exceeding 400 fathoms
to have no eyes, or to have rudimentary eyes without pigment. While exceptions to
this rule are rare in the shallow-water species, they are by no means unfrequent in the
deep-sea species. As to the structure of those eyes which may be called rudimentary,
they often have a distinct lens—a rounded spot marked by its brightness ; they are quite:
destitute of pigment, and, as I learned from a section of the oculiferous tubercle of
Nymphon robustum, Bell, the small eye has no retina, and is filled up with a mass of
detached connective tissue. .

In those species which are furnished with distinct eyes, the size of those on the same
tubercle is not always the same. In Mymphon strémii, Kroyer, the eyes which are
directed forwards are slightly larger than those which are directed backwards, but this
difference is much more marked in the species of Phowichilidium. This difference in size
—as is generally known—is a common occurrence. Grenacher’ has shown in the simple
eyes of the Arachnida and also of the larvee of many insects, that this difference in size
is often accompanied by extremely interesting differences in the minute structure. It

1 Grenacher, H.—Untersuchungen tiber das Sehorgan der Arthropoden, 40, Gottingen, 1879.
(ZOOL. CHALL. EXP,—PART x,—1881.) - K 16

122 THE VOYAGE OF H.M.S. CHALLENGER.

would be of interest to study this question in the Pyenogonida, but the limited number of
the specimens of the different species of Phowichilidiwm in the Challenger collection did
not allow me to study their eyes. I investigated those of Nymphon strémi, but there
the difference in size is slight ; I did not ascertain any difference in their structure.

The knowledge of the minute ‘structure of the eyes of the Pycnogonids is of very
recent date. They were always considered as simple eyes, and were even mentioned
as such by Cavanna. Dohrn, therefore, in the preliminary -publication on the results
of his studies on Pyenogonids, is the first who. gives us some information on these
organs. According to him the eyes, taken in a vertical. position, are of a pointed
oval shape;* they have a retina composed of modified epithelium cells (hypodermic
cells), the extremities of which are surrounded by a brown pigment; the cuticula forms
a lens. |

Among the latest investigations into the structure of the eyes of the Arthropoda, those
of Grenacher, published in his splendid memoir,’ have the merit in the first place not
only in proposing a homology between the parts composing a compound and those com-
posing a simple eye, but also in showing the existence of this homology throughout almost
the whole type of the Arthropods. Moreover, the value of his monograph with regard
to the physiology of the organ of sight, and the immense quantity of special information
which it contains, is at present almost inestimable. In investigating the eyes of the
Pyenogonids, I was extremely desirous to try whether the scheme for the eye of the
Arthropods, as proposed by him, would hold good also in the case of the Pycnogonids.
Though my researches did not give me a complete idea of the anatomy of their eyes,
I think my results are worth publishing here, because they admit of comparison with
the scheme given by Grenacher.’ ‘aie

I made numerous preparations of the eyes of different species of the genus Nymphon ;
of N. brevicaudatum, Miers, N. brachyrhynchus, Hoek, N. strémi, Kroyer, and of
the rudimentary eyes of Nynyphon robustwm, Bell. I studied more. especially those I
made of Nymphon brachyrhynchus and of Nymphon strémi. While the eyes of Nymphon
strénai (Pl. XVIIL. fig. 11, B) are comparatively small, and placed on the sides of a conical
tubercle, so as to be separated by a greater distance from one another below than above ;
those of Nymphon brachyrhynchus are larger, and are placed on the inside of a cylindrical
oculiferous tubercle, so close to one another as to meet at their inner surfaces. In fig. 2,

1 Von oben nach unten spitz oval (loc. cit., p. 37).

* Grenacher, H.—Untersuchungen uber das Sehorgan der Arthropoden, 4°, Gottingen, 1879. °

8 For studying the histology of the Arthropod’s eye fresh material, in the’ first place, is necessary. That I
got preparations fit to be used of the eyes of Nymphon brachyrhynchus, collected at Kerguelen Island, and put in
spirits in January 1874, is almost more than could be expected. In one respect only did the condition of the material
hinder me, viz., that I could not make use of some reagents, ¢.g., of nitric acid. Though used of different strengths, I
never obtained the solution of the pigment without the visual rods being destroyed also. Consequently I never got
a preparation showing the connection between the fibres of the optic nerve and these rods.

REPORT ON THE PYCNOGONIDA. 123

Plate XXI., I figure a longitudinal section of one of the eyes of this species; and in the
same figure the place occupied by the outer surface of the eye of the other side is indicated
(a). This outer surface is invested by a thin chitinous cuticle, which is minutely (longi-
tudinally) striped ; round the circumference it is in connection with the chitinous skin
of the animal. The inside of this wall is covered with pigment, and it is in this bed of
pigment that the union of the fibres of the optic nerve with the elements of the retina
takes place. I have already spoken above about the manner in which the optic nerve
penetrates the eye. I sometimes got preparations, which made me believe that the optic
nerve reached the outer integument of the oculiferous tubercle, at a considerable distance
below the eyes, and that it ran along this wall and penetrated the eye where it is in
connection with this integument ; this, however, is not really the case. Numerous
separate nerve fibres reach the under surface of the eye; they then penetrate its cuticle,
and in one of my preparations I observed distinctly, that they are in direct connection
with the rods of the retina.

In the interior of the eye there is a retina, but there is no distinct vitreous body.
I observed that under the thickened cuticula which forms the lens of the eye, just as
everywhere else, the epithelium (hypodermis) of the cuticula is formed of rudimentary
cells represented by nuclei. Of a distinct row of vitreous body cells, like those figured
and: described by Grenacher (Joc. cit.) and Graber, I observed nothing. Nor do I
believe that Dohrn’s assertion is right, that in the eyes of the Pycnogonida the retina
is derived from the epithelium cells (hypodermic cells). This retina consists of rod-
forming elements and of ganglion cells. Those parts of the rods which are directed
towards the fibres of the optic nerve are thicker and terminate abruptly (Pl. XXI. fig. 4),
bearing at the other extremity a long and filamentary appendage; while in other
preparations the retina elements which I isolated show the form figured in Plate XXI.
fig. 5,—viz., rods which imperceptibly pass. into thread-like appendages. In these
retinal elements I failed to’ observe any trace of the presence of nuclei. The thread-
like appendages of the rods extend till they reach the cuticular lens, A preeretinal
. lamella,- which, according to Graber, is characteristic of the stemma of the tracheate
Arthropods is not visible. Between the rod-forming elements numerous ganglion cells
- are observed in the. form of distinct rounded cells. I did not observe whether or not
they were really in connection with the filamentary appendages of the rods; but having
isolated from one of the preparations the rods, as figured in fig. 5, I found that the rod
passes into the filamentary appendage. Probably the. ganglion cells have also fila-
mentary appendages, which pass between the filaments of the rods. In this respect
' therefore my opinion is intermediate to those of Grenacher and Graber. This structure
is observed when the section passes vertically through about the middle of the eye

1 Graber, V.—Ueber das unicorneale Tracheaten-und speciell ‘das Arachnoideen-und Myriopoden-Auge. Archiy,
f, Mikr. Anatomie. XVII. 1880, p. 58-93, PI. v.—vii.

124 THE VOYAGE OF H.M.S. CHALLENGER.

(Pl. XXI. fig. 3). When the same (tangential) section passes through the lateral part
of the eye another structure is observed (Pl. XXI. fig. 2), viz., a mass of reticular tissue,
with numerous ganglion cells in its meshes, not unlike but a little smaller than those
between the rods of the retina. Empty cavities, from which, perhaps, ganglion cells
have dropped, are observed in it. A horizontal section of one of the eyes of Mymphon
strémii (Pl. XXI. fig. 1) shows the arrangement of these parts in the interior of the
eye. The middle part is that occupied by the retinal rods, which here have large
ganglion cells at their extremities, and a distinct mass of reticular tissue, separated
from the retinal rods by a thin membrane (2), is observed laterally. The dimen-
sions of the ganglion cells placed in the meshes of this reticular tissue in W% ymphon
brachyrhynchus are almost the same as those observed between the retinal rods; but in
Nymphon strémii the ganglion cells which are found at the extremities of the retinal rods
are much larger. In regard to the minute structure of these ganglion cells I have hardly
any observations worthy of being mentioned. The cells are always furnished with a
distinct nucleus, and their contents, as a rule, are granular. Those I observed between
the rods of Nymphon brachyrhynchus axe furnished with one filament directed towards
the lens.

The conclusions I have arrived at with regard to the anatomy of the organs of vision
in the Challenger Pyenogonids may be summarised as follows :—

(1.) A vitreous body, developed out of the cuticular epithelium (hypodermis), does
not exist.

(2.) The epithelium cells are present under the lens of the eyes in the same
condition as under the cuticula in general.

(3.) The retina consists of distinct rods and ganglion cells. Numerous ganglion cells,
placed in the meshes of a reticular tissue, form a mass, which encloses the interior of the
eye occupied by the rods.

(4.) The ends of the retinal rods reach the cuticular lens. A preretinal interlamella

_seems not to exist. ;

(5.) The retinal rods can not be considered as having resulted from transformed
hypodermic cells.

(6.) The retinal rods have two parts—an innermost thicker part and a filamentary
appendage.

(7.) The eye ig surrounded by a chitinous cuticula.

4, Alimentary Canal and its Appendages.—I only occasionally got preparations of
the alimentary canal; therefore what I have observed in regard to this organ is far
from exhaustive.

Physiologically, this is perhaps the most interesting organ . of all, and, morphologi-
cally, its signification is by no means small, as its structure has, along with the number

REPORT ON THE PYCNOGONIDA. 125

of the legs, always been considered as a very important support for the beliet in the
near relationship between the Pycnogonida and the Arachnida, and more especially
the Phalangida. ; .

Morphologically, the cesophagus extends from the mouth. to behind the cesophageal
commissures.. Taking the function of the organs into consideration, I believe that only an
extremely small part should bear the name of cesophagus. At a very short distance from
the mouth the cesophagus widens considerably. This widened part, which shows its
greatest dilatation in front of the middle of the proboscis, slopes again backwards, and
imperceptibly passes over into a much narrower canal, which extends immediately
behind the cesophageal commissures. The widened part of the cesophagus, which almost -
reaches to the end of the proboscis, is invested by a chitinous wall. This wall is beauti-
fully beset with thin parallel chitinous bands, which are furnished with numerous thin
spines. In the front part these are wanting. They begin on the two ventral parts of the
inside a little before they are found on the dorsal part. These foremost spines have the
form of short teeth, and only further back do they assume the form of long thin spines
or needles. From the wall of this ‘part of the cesophagus numerous bundles of trans-
versely striated muscles extend till they reach the outer wall of the proboscis, their
distribution bemg in Nymphon, e.g., such that two longitudinal rows are attached
to each of the three parts of which the inner wall of the cesophagus is composed
(Pl. XVIIL fig. 9). As to the function of this part of the cesophagus, judging from
these muscles and from its internal armature, I think it not very hazardous to com-
pare it with the cardiac portion of the stomach of the Crayfish. It is a masticating
apparatus.

Posteriorly it passes over into a very long (slender species of Nymphon), or rather
short (Colossendeis) cylindrical tube, the wall of which is still divided into three longi-
tudinal parts, which on a transverse section are triangular and leave an extremely narrow
canal in their middle. I studied the histological structure of this part of the wall, which
extends to beyond the cesophageal commissures. Its cells are of a long cylindrical form,
longer in the middle and shorter on both sides of the triangular part. They are furnished
with distinct nuclei, which sometimes are all placed near the outwardly directed extremity
of these cells, but sometimes also are found more in the middle. Between these cylin-
drical cells there are some of a long conical shape, the base of the cones being, as a rule,
— directed outwards. Inside, the surface of these cells is invested by a structureless membrana
intima, and outside a similar cuticular formation is present (Pl. XXI. fig. 6). This
epithelial covering does not end abruptly immediately behind the cesophageal commissures.
In the interior of the succeeding part of the intestine it forms three glandular bodies,
which hitherto have not been observed, and whose function, judging from their position,
must be, I believe, pancreatic. In fig. 7 on Plate XXI. I show the place occupied by these
glands, and in fig. 8 of the same plate a transverse section near the extremity of the two

126 | THE VOYAGE OF H.M.S. pee

undermost glands is figured. These sara project into the interior of the intestine, and.
are, as far as I know, the only true glandular bodies which stand in connection with the
alimentary canal. They are invested by the same membrana intima as the wall of that
part of the cesophagus, at the end of which they are found. The form of the cells which
compose them is nearly the same. The whole of the gland must be considered as having
taken its origin from an excrescence and bending towards the wall of the intestine, of the
- hinder part of that cesophagus. .
In regard to the structure of the remaining part of the intestine I do not wish to
- enter into any details. I only observed that the structure of the wall of that part which
follows immediately after the cesophagus, and of the caeca, which penetrate as a rule
as far as the sixth joint of the leg, is nearly the same. We find this wall everywhere beset
with extremely numerous tubes or villi, which in some genera (Nymphon) are of a
shorter and more rounded form, and in others (Colossendevs) are very slender and almost
cylindrical. While the outermost part of the wall is formed of a single row of large
distinct nucleated cells, these villi show a multi-cellular structure also. Each of these
cells contains numerous globules, which for the most part seem to be of a fatty
nature. The form of the cells is different, but they are commonly rounded. I call
them cells, because each of the bodies has a distinct oval nucleus with a small nucleolus.
As has been observed by almost all authors writing on the structure of the wall of the
intestine, these cells often become detached from the wall, and are found lying loose in
the contents of the alimentary canal. The nuclei in the cells of these villi were by no
means easily observed in all the sections I studied. They were very distinct in the cells
of the villi of Colossendeis proboscidea, Sab. (sp.).

It seems to be characteristic of the genus Colossendeis that the ceca destined
for the different legs should branch off from the main duct, which runs straight from the
proboscis to the abdomen, very close to one another, and close also to the place where the
cesophagus communicates with the intestine; at least I observed that in the three species
of Colossendeis I studied (Pl. XVII. fig. 1). The number of lateral cxca given
off at both sides of the main duct is six-in Colossendeis. Of these the first two are
rudimentary, one being the rudiment of those destined for the mandibles, the other (the
first lateral pair) being that for the proboscis. Each of the four remaining ceca, of.
which the hindermost pass through a much longer part of the body before penetrating the
leg than do the more anterior ones, shows a considerable swelling in the lateral processes,
at the ends of which the legs are inserted.?. The anal aperture of Colossendezs (Pl. XVII.

.fig. 1d) is an oval-shaped slit. It is not placed terminally or in the median line of the
abdomen, but laterally.

1 On a transverse section of the body of a Colossendeis between the lateral processes for the second and for the
third pair of legs, five round sections of the intestine are seen placed close to one another. This furnishes a good
opportunity of comparing their structure, but no difference is observed. Compare fig. 14 of Plate XXI.

REPORT ON THE PYCN OGONIDA. 127

In Nymphon the number of lateral cxca of the alimentary canal is five pairs. Of
these the first pair is very wide and directed forwards. At the base of the proboscis
it divides into two branches. One (the larger one) is directed upwards and forwards,
and penetrates the mandibles ; the other one enters the proboscis and divides, in some
species (Nymphon brachyrhynchus, e.g.), again into two branches. These extend in some
species farther than in others, but I never observed them beyond the hindermost half of
its length. :

The groups of comparatively large cells with very thin walls and distinct nuclei, each
of them containing, as a rule, one (sometimes more) strongly refracting granule probably
have also some relation to nutritive functions. These I observed in ymphon, Phoxi-
chilidium pilosum, and in Colossendeis, collected in large groups sometimes about fifty
in number. They seem not to be limited to any particular part of the body, but I
found thém always in the neighbourhood of the muscles, between the connective tissue,
where fibrous threads keep them in place. I feel inclined to consider them as analogous
to the fat-cells of most Arthropods. I figure a group of them in Pl. XXI. fig. ..9)

5. The Circulatory Apparatus.—The somatic cavity is divided into distinct compart-
ments, by means of sheets and bands of fibrous tissue. One of these, placed between the
dorsal wall of the intestine and the dorsal integument of the body, is furnished with
contractile walls, and has the function and the structure of a heart: In Colossendeis this
heart is not surrounded by a pericardial sinus (PI. XXI. fig. 14, h, Pl. XVII. fig. 1). The
blood, entering the apertures of the heart, comes directly from one of the longitudinal
compartments into which the somatic cavity is divided. The contractile walls of the heart
do not enclose it on all sides ; for on the dorsal side a part of the integument is used to
form the dorsal wall of the heart. The contractility of these walls is due to the presence
of muscles, which run in a transverse direction and are not striated. Along both sides
of the heart these muscles are inserted into the dorsal integument of the body. As
to their structure, I observed their fibres to be extremely thin and slender. When
studying them with a strong lens (e.g., 11, Immersion of Hartnack) I observed that they
exhibit parallel edges only for a certain distance ; for this pagallelism almost imperceptibly
passes over into an extremely feeble swelling of the fibre, in the interior of which a
long nucleus with a distinct nucleolus is observed.

The heart of the Pycnogonids, as a rule,’ is furnished with three pairs of apertures.

‘ In one specimen of Nymphon brachyrhynchus I observed that one of the branches penetrating the proboscis
divided again, so that in the same section, through about the middle of the proboscis, five sections of intestinal ceca
were observed. This I consider of no importance at all. It only proves, I believe, that it is almost dangerous to
attribute any fundamental value to the number of pairs of cca arising from the intestine. In a large specimen of
-Pycnogonum litorale a section of the fourth joint of the leg shows two sections of ceca in the same joint: the cecum
has given off a branch. Consequently I believe that the number of these branches depends in general upon the capacity
of the different appendages. In Nymphon and Colossendeis no ceca are observed entering the palpi and the ovigerous
legs, only because the capacity of these extremitiés does not allow of it.

“2 Not always. Pallene brevirostris, Johnston, ¢.g., has only two of these.

-

128 THE VOYAGE OF H.M.S. CHALLENGER.

The first pair are placed on the sides of the heart opposite to the second pair of legs; °
the second pair are placed similarly, but opposite to the third pair of legs; the
third pair are found near one another at the posterior extremity of the heart. Through
these three pairs the blood is admitted into the heart,’ while it leaves it through a large
opening placed at its anterior extremity. No aorta or arteries arise from it. In the
heart of the specimens in spirits of Nymphon robustum and some other species I
observed a compact mass of blood-plasm, which ‘so totally filled up the cavity of the
heart as to give, after having been taken out, an exact figure of its form.

As to the blood-cérpuscles I only observed that they are, in Nymphon and Colos-
sendeis, round and flat bedies with a distinct nucleus. However, I observed also more
irregularly-shaped fusiform bodies, especially numerous in the cavities of the skin of
Colossendeis (Pl. XVIII. fig. 1). With regard to their shape and dimensions there is no
great conformity between the opinions of Cavanna and Dohrn ; however, it is only the
study of fresh material that can finally settle such controversies.”

6. Genital Organs.—About the testis of the Pycnogonids hardly anything is known ;
and this cannot be wondered at when one considers that the true males were only dis-
covered by Cavanna in the year 1875, the animals with swollen thighs described as males
before that period being really the females. However, even Cavanna does not seem to have
correctly identified the male organs, for he places them in the fourth joint of the legs. .
Dohrn has been the first, and hitherto the only one, who has pointed out the true position
occupied by the testis, “‘ Die Hoden liegen im Kérper der Pyenogoniden, nicht in den
Beinen, und bilden dort jederseits einen Schlauch, welcher in jede Extremitiit seiner
Seite einen kleineren Schlauch absendet, der an der obenerwihnten Stelle in einer runden
Oeffnung endet.” This description, true in the main, is, however, not applicable to all
the species of Pyenogonids ; for, from what I have observed myself, I am able to furnish
full evidence that, for some species, Dohrn’s description is not quite correct.

A large specimen of a male Colossendeis proboscidea, figured of the natural size in
Plate XXI. fig. 10, has been opened on the dorsal side. The skin with the heart being
removed, the testis is observed in situ, and the intestine may be distinguished below
it ; the male organ, therefore, is placed rather at the dorsal side of the body.

The two laterally and longitudinally running parts of the organ are united posteriorly

1 From observations I made, in the summer of 1880, in the laboratory of Prof. Lacaze-Duthiers at Roscoff.

2 Cayanna calls them “ piccolissimi globuli ellitici o sobellittici.”. Dohrn, on the other hand, describes the blood-
corpuscles as “ungewohnlich gross und complicirt.” According to Dohrn, there are two forms of blood-corpuscles—“die
einen bilden einen blassen, suzammengefalteten Ballon, in dem ein etwas gliinzenderer linsenformiger Kern sich findet
neben 3—4 grossen Vacuolen; die anderen sind deutliche Amében, mit lebhaften amodboiden Bewegungen und
umschliessen oder tragen eine gréssere Anzahl glinzender Trépfehen.” It seems to me that the iarge balloon-forming
elements come very near to my fat cells (see p. 127) ; and as to the ameboid corpuscles, these are probably my fusiform
elements and the elliptic ones of Cavanna, If Dohrn is right about his large blood elements, then the animals must
have still others of a third form.

REPORT ON THE PYCNOGONIDA. 129

by a commissure, so there is only one true testis, which has the form of a capital U.
From the upstrokes of this U, on both sides, those parts originate which penetrate
the leg, and which extend almost to the end of the fourth joint. The two parts of the
testis which run longitudinally through the body are broad and flat ; their course is not
straight but rather undulated, being bent outwards whenever a lateral branch takes its
origin. Although the organ is placed at the dorsal side of the body and legs, the
male genital pores are situated ventrally towards the end of the second joint of each leg.
This external opening is very small and is at the tip of a distinct conical tubercle. It
leads into a canal which runs backwards almost parallel with the margin at the distal
. extremity of the joint and closely adheres to its chitinous covering ; this canal runs
along the wall of the joint till it reaches the dorsal side of the leg, here it becomes wider
and turns inwards till it reaches the testis, which shows a small knob facing the beginning
of the canal. Plate XXI. fig. 11, shows these particulars; the joint is figured as trans-
parent, and the muscles which run from this to the following joint are to be considered
as removed. ‘The outer part of the canal, from the opening for about one-fourth of its
length, is furnished with a thicker wall, and this shows most probably the extent to
which the chitinous covering of the leg is bent inward. The remainder of the canal
is formed of connective tissue,—at least I failed to observe an endothelial covering,—
lined externally by a distinct muscular layer, the fibres of which run longitudinally
and are not striated (Pl. XXI. fig. 13).

As seen in fig..2, Plate XVIII., that part of the testis which penetrates the leg is in a
transverse section kidney-shaped ; a longitudinal duct is formed between the gland and
the thin tissue or membrane which it touches laterally at two points. Most probably it
is with the duct so formed that the canal which opens at the distal extremity of the
second joint is in communication. :

I have observed nearly the same structure of the male genital organs in the
extremely transparent species of Nymphon, to which I have given the name of Nymphon
perlucidum (p. 50 of this paper), and also in Nymphon robustwm, Bell. Both species
show genital pores in the male sex, only on the two hindmost legs; and quite in cor-
respondence with this observation only two pairs of lateral excrescences of the U-shaped
testis are to be seen. So when Dohrn says, for Pycnogonids in general, that the male
organs penetrate each leg and open in a round pore on the ventral side (which is,
no doubt, the case in all the species examined by him), he is laying down a
rule which admits of a great many exceptions; fer among the Pycnogonids dredged
by H.M.S. Challenger there are species having their male genital pores only on the
two hindmost legs; again, there are some which possess them on the three hindmost
pair of legs, and, finally, there are species with pores on all the legs. My doubts about
this point were cleared up by the observation of those species which. bear their male
genital pores at the tip of a stout cylindrical outgrowth (species of Ammothea, e.g.).

(ZOOL. CHALL. EXP.—PART. x.—1881.) K 17

130 THE VOYAGE OF H.M.S. CHALLENGER.

Of course the non-existence of a hardly distinguishable structure cannot be con-
sidered proved merely because the structure has not been observed, even in numerous
specimens of the same species. But, on the other hand, if the structure is very
easily seen in some specimens, we are at liberty to conclude that it is absent in those
cases where it was not observed. Moreover, it is hardly possible. that in those
cases where the pores are only observed on the two hindmost legs, they should be
present also on the foremost, and from some unknown circumstance should continually
escape observation.”

In regard to the microscopical structure of the testis I have not much to say. Ona
transverse section numerous extremely minute cells are observed (see Pl. XXI. fig. 12),
while that part of the testis which adjoins the longitudinal canal has lost its cellular
structure, and shows a rather granular condition. Whether these granules are the sper-
matozoa, or whether the numerous globular bodies each furnished with a filamentary
appendage on one side which I once observed, when pulling to pieces with’ needles a part
of the testis, are the spermatozoa, cannot, of course, be ascertained from animals in
alcohol, even when preserved so well as the Challenger specimens are. Only in mature
animals do the male organs attain the development figured for Colossendeis proboscidea.
This, most probably, is only the case during a short period of the year, considering
moreover that the males in most species seem to be less numerous than the’ females
(ten female Colossendeis proboscidea and only one male, twelve female Colossendeis
leptorhynchus, and only one male, &c.), it cannot be wondered at that the number of
species in which I could investigate these organs was limited. Except in Colossendeis
proboscidea, and in three species of Nymphon, I observed the testis also in the
leg of Ascorhynchus glaber (Pl. XVI. fig. 9, x), but here only in the fourth joint of
the leg.

In the other specimens. which I consider as males, the only means I had to make
out the sex consisted in looking for external sexual characteristics, such as are afforded
by the dimensions of the genital pores and the condition of the thighs. Large genital
pores and swollen thighs are characteristic of the females; slender thighs and small
pores, very often not present in the first or in the first two pairs of legs, are characteristic
of the males. Moreover, a transverse ‘section of the thigh of one of the legs is easily
made, and does no injury worth mentioning to the specimen. When in such a section
no ovary is observed, so far as my experience goes, it is almost certain that the

1 The genital pores of Nymphon robustwm, Bell, g, are tolerably large, and are easily observed with the aid of a
magnifying glass. Yet I have examined large specimens of this species (dredged in the Barents Sea), where these pores
were not observed, even when investigating. the joints with the microscope. As I was convinced of the exactness of
this observation, I felt greatly puzzled with it at first ; afterwards on reading a paper of Schobl in the Archiv f. Mikro-
skop. Anatomie, Bd. xvii., 1880 (Ueber die Fortpflanzung isopoder Crustaceen) I found that this author admits that in

_ the females of these Gatien the genital pores are only present at a certain period, and are totally wanting during
the rest of the year. Perhaps there are male Pycnogonids which have the same peculiarity.

REPORT ON THE PYCNOGONIDA, 131

specimen is a male ; even in very young females at least a trace of. the ovary is always
to be observed in those joints.

_ According to Dohrn the female glands are disposed in the same way as the testis,
with the only difference, that in the ovaries of most species, the lateral excres- *
cences which penetrate the legs and often force their way into the penultimate joint,
are the only parts which develop mature eggs.

What I- happened to observe agrees almost completely with Dohrn’s description.
I perfectly believe, however, that. the occurrence of a part of the ovary in the body of a
Pycnogonid is rather rare, because, as a rule, only the lateral excrescences remain.
No doubt this must be considered as a secondary condition; and seeing that, so far
as I could ascertain, it is the rule in all the species of Nymphon, my original opinion,
that the genus Nymphon, of all the genera of. Pycnogonida, resembled most the
hypothetical ancestors of our group, was severely shaken.

The genus Colossendeis affords a beautiful example of the original condition of the
ovary. I examined a specimen of Colossendeis leptorhynchus, Hoek. A transverse
section of the body showed the place occupied by the ovary, and convinced me of the
exactness of Dohrn’s assertion. However, as in the case of the testis, Dohrn’s observa-
tion is incomplete in one respect ; there are not two ovaries, but only one. Immediately
in front of the abdomen the two lateral parts are united by a cross- piece, and so the
ovary has the very same shape as the testis, viz., that of a U with long upstrokes.
That it occupies also the same position in the body as is the case with the testis, is clearly
seen in fig. 14, Plate XXI., which is a drawing of a transverse section of the body. In
o. the ovary is shown pled above the intestinal tract and its excrescences which pene-
trate the legs. The dimensions of the eggs in that part of the ovary which is situated
in the body are, at least in this species, the same as of those eggs which are found in the
thighs of the legs. The lateral excrescences penetrate all the legs, and in the specimen I
studied reach the sixth joint. This, most probably, will greatly depend on the state of
maturity of the animal. I often found the eggs only in the thigh, but often also (Han-
nonia typica, Hoek, Pl. XIV. fig. 11, e.g.) the eggs are found as far as the end of the
second tibial joint. The ovary is always placed dorsally to the intestinal tract, which
is also the case with those animals which have only the lateral excrescences left, and
thus show several ovaries.

The structure and the formation of the ovarian eggs I will describe further on. In
regard to the way in which the eggs are laid, I had the good fortune to observe the
copulation of a male and female Phoxichilus laevis, Grube, when I was, last summer,
in the zoological station of Professor H. de Lacaze-Duthiers at Roscoff. The eggs
are fecundated the moment they are laid, and’ the copulation, therefore, is quite
external, brought about by the genital openings of the two sexes being placed against
each other. Half an hour after the beginning of copulation, the male had a large

132 THE VOYAGE OF H.M.S. CHALLENGER.

white egg-mass on one of his ovigerous legs, and about one hour later both masses were
present. 5 :

The female genital openings.are a great deal larger than those of the male, and are of
an ovate shape, and, as a rule, oviducts are totally wanting. I only observed them in
the genus Colossendeis, where they have nearly the same course as the vasa deferentia.
Nearly in the middle of the second coxal joint of the two hind legs a lateral branch
arises from the ovarian coecum, which passes through the joint. The interior of this
branch, which is the oviduct, is in immediate communication with the ovary, and during
the breeding season the eggs are found penetrating the branch. While the ovarian cceca
which penetrate the legs are lined only by connective tissue, the oviducts which
begin at the dorsal side of the second coxal joint and run along the wall of the joint till
they reach the opening on the ventral side, are lined by a coat of longitudinal muscle fibres.
The female genital opening in this species is small and rather triangular.’

From the end of the oviduct which reaches the opening, distinct muscle fibres
radiate, and are inserted round the opening on the inside of the chitinous wall of.
the joint. A transverse section of the fourth jomt of the leg of a female Colossendeis—
leptorhynchus is figured in fig. 16, Plate XVI. ; m is the ovarian ccecum which, as this
specimen is by no means mature, is only of small dimensions; when in the breeding
season, the whole central cavity (which in the figure is represented as empty) is filled
with eggs ; it swells to such an extent as to fill up almost the whole cavity of the leg,-in
so far as this is not occupied by the intestinal ccecum. As in the other species of
Colossendeis, the eggs are extremely numerous and small. Each ovarian ege has a
distinct germinal vesicle, which is placed almost exactly in the centre of the egg, and
has, as a rule, one distinct and very glittering germinal spot. Among the older eggs,
which are richly furnished with yelk, smaller ones are always observed whose protoplasm
is almost quite transparent. Each ege is surrounded by a very thin membrane, which is
a true ‘‘vitelline membrane” and adheres closely to the protoplasm of the egg.

In the genus Nymphon, I have investigated the female genital organs of the follow-
ing species :—Nymphon brevicaudatum, Miers ; N. brachyrhynchus, Hoek ; N.-robustum,
Bell; NV. longicowa, Hoek; and N. hamatum, Hoek. I never observed the ovary in
the body of these species, and always found at least a trace of it in the fourth joint of
the leg (thigh). R

When in an early stage.of development, the ovary is placed against and at the dorsal
side of the intestinal ccecum which passes through the jomt. While the ripe ova, which

‘are often very large (Pl. XVI. fig. 7 7, ripe ovum of Nymphon brevicaudatum, Miers),

have a thin vitelline membrane as in the ovum of Colossendeis ; younger ova have often the

1 In this species, as I have mentioned already (p. 63), the genital openings, both in males and females, are present
only on the two hind legs ; at least in all the specimens at my disposition, I failed to observe them on the first two
pairs of legs. However, ovarian cceca penetrate the first two pairs of legs as well as the two others.

REPORT ON THE PYCNOGONIDA. . . 133

appearance of being surrounded by a very thick and concentrically stratified membrane
(ovarian egg of Nymphon brevicaudatwm, Pl. XXI. fig. 15). In other species (Vymphon
robustum, Pl. XXI. fig. 16) this membrane is perfectly transparent, while in both cases
the granular protoplasm of the egg within this thick membrane or capsule seems to be
surrounded by its vitelline membrane. In a third case, which I observed in Nymphon
longicoxa (Pl. XXI. fig. 17), the membrane of the egg does not seem to be thick, but
nregularly folded and crumpled ; yelk-particles are here very numerous in the central part
of the egg, which surrounds the germinal vesicle; and the protoplasm of the egg extends
beyond this central part till it reaches the crumpled membrane. However, it is very
probable that the condition of the eggs has suffered from their having been so long in
alcohol, only I wish to point out that from what I observed it is almost certain ‘that
any one studying the formation and the development of the animal egg, will find a very
interesting object in the egg of the Pycnogonida. The dimensions of the mature ova
are very different. Of the specimens I studied they are largest in Nymphon longicoxa,
N. brevicaudatum, and N. robustum, a great deal smaller in N. brachyrhynchus and
N. hamatum (the number of egos Ss in an egg-mass being always in inverse propor-
tion to their size).

While in the younger ovarian eggs the ata vesicles as a rule are placed in the
centre of the egg, in the very large mature egg the vesicle is placed close to the wall.
Sometimes (Mymphon longicoxa) it has the shape of a sand-glass, and once I observed an
extremely small micropyle canal in the membrane of the egg, just opposite the place
oecupied by the germinal vesicle. As a rule there i is only one germinal spot, but I once
observed two distinct:spots in the germinal vesicle of the egg of Nymphon longicoxa. In
the ovarian egg of Nymphon robustwm one distinct nucleolus may be observed almost
exactly in the centre of the rounded and granular germinal spot. As for the manner
in which the eggs make their way to the genital apertures in those casés in which no
true oviduct is observed, I think there can be no doubt that the body-cavity itself per-
forms the function of an oviduct. The absence of such a duct at the genital pores,
and the fact that I repeatedly observed detached eggs pressed against the connective
. tissue surrounding the ventral ganglia. or other parts in the interior of the body admits

of no doubt in this respect. z

All I have said about the ovary and the formation of the ova in the genus Nymphon
also holds good in the case of the other genera. The limited quantity of specimens
prevented me from making a section of the body of species of these genera. Most
probably Ascorchynchus will show the same disposition as Colossendeis. A transverse
section of the thigh of one of the legs of Ascorchynchus orthorhynchus is figured in
Plate XVI. fig. 11. The thigh is much more dilated than one of the other joints of the
leg, yet it is not round but flattened, and the contents are almost divided into two un-
equal parts by the large chitinous thickening, which at the one side is in conhection

134 THE VOYAGE OF H.M.S. CHALLENGER.

with the wall of the leg. The one part is filled up with the ovary, the other partly with
the ccecum of the intestine. The ovarian eggs are small and are furnished with a ~
central germinal vesicle. Most probably the females of the species of Ascorhynchus have
an oviduct like that of the species of Colossendeis. The species of Pallene show the same
disposition as in Nymphon. A transverse section of the thigh of Pallene australiensis
corresponds perfectly with that of NMymphon breviccudatum, figured -in Plate XVI. _
fig. 7; there is one very large and probably mature egg with an eccentric germinal
vesicle, and numerous smaller ovarian eggs, with their vesicle in the centre. Moreover,
minute researches .on Pallene brevirostris (an inhabitant of the Dutch coast) admit of no
doubt as to the structure of the ovaries; they are totally wanting in the body, and take
their origin in the thighs of the legs. The eggs when mature are large, and their number
is limited.

In the genus Phowichilidium I studied the anatomy of the body of Phoxichilidium
pilosum (as female specimen) without meeting with the ovary. In the legs of this
species, however, and also of Phowichilidiwm patagonicum, I soon found it. The
whole cavity of the leg is often filled up with eggs, and these are éven observed
pressed closely against the wall of the leg (Pl. XVI. fig. 17). The eggs are comparatively
small and very numerous. The membrane of the eggs is much thicker than is the case
with the eggs of the other genera (Pl. XXI. fig. 18). Neither in the species of Padlene
nor of Phoxichilidium did I observe the least trace of an oviduct, so I think that here,
‘as in Nymphon, the genital aperture communicates directly with the cavity of the leg.
I think also that the circumstance I often observed of eggs free in the cavity of the
leg is in support of this opinion (Pl. XXI. fig. 18). For the other genera of Pyenogonids
I have, so far as the ovaries are concerned, no observations worth mentioning.

7. Observations on the Embryology of the Pycnogonida.—Among the Pycnogonids of
the Challenger Expedition there were some species provided with eggs. On account of
the great importance of embryology for the study of the affinities of a group of animals
I tried to acquire as much information on this subject as possible. Unfortunately, with
the exception of one species belonging to the genus Ascorhynchus, G. O. Sars, all the
species with egg-masses belong to the genus Nymphon, Fabr., but of these there are out
of twelve species no less than: six provided with eggs.

The researches of Kroyer, Johnston, Goodsir, Dohrn, Semper, Cavanna, and eeeale
have shown that in the geriera Pycnogonum, Pallene, Phoxichilus, Phoxichilidium,
Nymphon, &c., the eggs after having been laid are carried on the so-called ovigerous
legs. The honour of having discovered that not the females (as was believed by the
older authors) but the males fulfil the duty of bearing these eggs is due to Cavanna; this
observation has since been confirmed by the researches of Dohrn, Bohm, and myself.’

1 The observations of Cavanna were published in the year-1875. It is indeed strange to see that neither Wilson
nor Miers have heard of this discovery. These authors, in their descriptions of new species, &c., are therefore almost
constantly confounding the two sexes. - :

' REPORT ON THE PYCNOGONIDA. - 135

In the first place, however, | wish to draw special attention to the fact that with regard
to Nynuphon brevicaudatum, Miers, this rule admits of an exception. JI examined a species
with large genital pores and swollen thighs, and provided with egg-masses on the ovi-
gerous legs. On investigating transverse sections of the thighs, I soon saw that this
specimen was a female. So far as I know, this is the first time that an exception to
this rule has been observed. In the second place, I wish in a few words to discuss

-the circumstance that, although eight different species of the genus Colossendeis were
collected (together represented by thirty-one specimens, and four specimens of Colos-
sendeis proboscidea, Sab. (sp.), trawled north of Scotland during the cruise of the
“ Knight Errant ”), none of these are provided with eggs. The number of males, however,
is very restricted: there is only one male Colossendeis leptorhynchws among nine speci-
mens, there is one male Colossendeis gigas among six specimens, one male Colossendeis
megalonyx among seven, and, finally, one male Colossendeis brevipes. On the other hand
it is possible that the genus Colossendeis is an exception to the rule, and that the males
in this genus may not have the gallantry to nurse their babies as the males of. the species
of other genera are accustomed to do. For, comparing the ovigerous legs of the males
with those of the females, a distinct difference is almost always easily observed: those of
the males are a great deal stouter, the fifth joimt is as a rule swollen towards the
extremity, or furnished with a distinct knob, &c.; but im the ovigerous legs of the

males of the species of Colossendezs, these differences in form and size are never observed.
So it is quite possible that they deal differently with their eggs from the species of
other genera.

’ The species provided with eggs are: Mymphon hamatum, Hoek ; N. eae Hoek ;

nies Hoek; N. brevicollum, Hoek; N. brachyrhynchus, Hoek; N. ieee
datum, Miers : and Ascorh ynchus minutus, Hoek. Of the latter species there are in
all two specimens, and of these one bears eggs. But the development of these eggs is
in its last stage, so that I was only able to ascertain the form of the larve. The eggs of
this species are extremely small, and at the same time numerous.

It consequently happened that my embryological researches were limited to the genus
Nymphon ; in so far not unfavourable, as yet almost nothing has been published on the
embryology of this genus.

Full-grown males of the genus Nymphon bear the eggs on the fourth and fifth joints
of the ovigerous leg, or only on the fifth joint; the curious foliaceous appendages occur
on the sixth to the tenth joints of the leg, and have nothing to-do with the egg-bearing
function of the leg. Yet it is possible that they may be of some use in seizing the eggs
when just laid, but, on the other hand it must be observed, that in the genera where
these appendages occur, the ovigerous legs of the females are furnished with them as
well as those of the males.

The eggs are soldered together and form in the species of Ny ymphon I spied! and

: “ .
136 THE VOYAGE OF H.M.S. CHALLENGER.

in Ascorhynchus minutus, one packet only on each ovigerous leg. I believe, however,
that cases are by no means rare in which two or even three packets are formed on one
ovigerous leg... The packet is placed round the leg, and in some species (Nymphon
brachyrhynchus, Hoek, e.g., Pl. XIX. fig. 1), it may be easily brushed off. In other
species, however, Nymphon robustum, Bell, for example, this is by no means so easy, the
surface of the joints of the ovigerous legs being furnished with numerous hook-like
spines.

Every egg in the packet has its own membrane, a very thin and structureless tunic.
The size of the packets is very different. It varies greatly with the size of the animal,
but is different also in different specimens of the same species. The size of the egg
seems to be constant for every species ; consequently the size of the packet will depend
on the number of eggs in each packet ; and the age and the condition of the female will,
of course, influence this.

The egg of Nymphon brevicaudatum, Miers, measures 0°5 or 0°7 mm. ; when in the
first stages of development it is nearly globular (0°6 x 0°6 mm.), afterwards oval (0°5 x 0°7
mm.). The number of eggs in each packet varies between fifty and sixty. The egg
of Nymphon fuscum is a great deal smaller (0°15 or 0°12 mm. The eggs of Nymphon
brachyrhynchus are about 0°55 mm. and even in a much advanced stage of development
nearly globular. Large packets of the latter species do not contain more than fifty eggs,
and the dimensions of these packets vary between 3°14 x 1°85 mm. and 2°3 x 1°6 mm.
The ege of Nymphon brevicollum has a diameter of 0:26 mm.; the number of eggs in a
packet is in this species about ninety. Fig. 2 on Plate XIX. gives a section of a
packet of eggs of this species. The colours are those which are seen when the
object is coloured with picrocarmine, and the figure is half in outline ; every egg is seen
to be placed in a cavity formed by the cement which solders the eggs together (c), and
- coloured distinctly red by the, picrocarmine. The large opening (0) in the centre is
that occupied by the ovigerous leg ; the small holes (s, s) are those which are left between
the eges when soldered together. On the outside mud and sand particles adhere to the
packet (m).

So far as I know, Dohrn is the only author who has published observations on the
cleavage of the Pyenogonid egg ;' but as the method of making sections of such very
small eggs was not yet in use when he published his paper, and could not, theréfore,
he applied by him, I might reasonably have expected to see much more than he did, by-
availing myself of this method of recent embryology. Yet my researches in this respect
were not very successful, owing at least partly, I believe, to. the condition of the material
I studied. Every one will acknowledge how necessary it is, especially in embryological
researches, to study fresh and also very rich material ; now the Challenger Pyenogonids
had been six or seven years in alcohol before I studied their eggs, and, moreover, the

1 A. Dohrn, Ueber Entwicklung und Bau der Pycnogoniden, Jenaische Zeitschrift, Bd. v., 1869.

REPORT ON THE PYCNOGONIDA. 137

quantity was limited, so I need not appeal to the indulgence of the reader on account
of the imperfection of my researches in this department.

The study of the eggs of Nymphon brevicaudatum, Miers, was the most successful of
all. These eggs are the largest of the species here in question; the number of animals
furnished with eggs was in this species rather great ;1 and their condition was superior
to that of the eggs of the other species. The method I followed is well known. I
enclosed the eggs (hardened with absolute alcohol) in paraftine, and coloured the sections
afterwards with picrocarmine.

Fig. 3 is a drawing of the first stage I was able to observe. The food-yolk and the
formative-yolk (deuto- and proto-plasma, Ed. van Beneden) are still mixed together, and
the cleavage is complete. Every segment is furnished with a nucleus, coloured distinctly
red by the picrocarmine, and situated almost in the middle of each segment. The structure
of the yolk particles in each segment is very curious, and probably this is caused by
the continued action of the alcohol. In fig. 4 I give a strongly-magnified drawing of a
small part of such a segment just at the border of the section. It looks as if the yolk-
elements had grown vesicular,—a matter I only make mention of as the same structure
is no longer observed in the next stage of development of the egg. In this stage, as in
the following, the egg is furnished with a distinct but very thin membrane.’

The second stage I observed has the blastoderm distinctly developed. The cells of
which it is composed are very much flattened, and do not show distinct limits; a very
large nucleus is, on the contrary, always easily observed. Fig. 5 shows the cells as seen
on section, fig. 6, the blastoderm with the nuclei magnified. Every nucleus shows a
distinct nucleolus and numerous small granules. In this stage the food-yolk is irregu-
larly split into larger or smaller parts, which are coloured yellow by the picrocarmine ;
they do not show the vesicular structure of the yolk-segments in the first stage, and are
not furnished with a nucleus.

A transverse section of the next stage of development I observed is figured in fig. 7.°
Here the embryonic development is already far advanced, consequently I was not able

1 The eggs of Nymphon hamatum, N. longicoxa, and N, fuscwm were so far advanced in development that in them
only the different larval stages could be studied.

2 Dohrn, loc. cit., p. 139, says that the egg of Pycnogonwm litorale has a double membrane, and that these membranes
are found in the ovary, an assertion not corresponding with the observations I made on the eggs of Nymphon.

3 Between the stage figured in fig. 7 and the foregoing, numerous other stages were observed ; but in these the cel-
lular structure was so totally spoiled by the action of the alcohol, that I dare not give drawings or descriptions
of them. The only means of distinguishing the embryonic cells from the deutoplasm is by the colouring of the
cells with picrocarmine, and there can be little doubt that one of the first changes the blastoderm undergoes con-
sists in the formation of a longitudinal thickening of it at the future ventral side of the embryo. This thickening
terminates rather abruptly at the anterior end, but at the posterior end it slopes gradually to the unicellular part
of the blastoderm. Afterwards a longitudinal furrow seems to take rise in the middle of this thickening, the inner
part of which is finally isolated in the form of a longitudinal tube. I publish these details only with the strongest
reserve, the condition of the eggs and the circumstance that the sections are necessarily taken in quite uncertain
directions, making the giving of a decided description impossible,

(ZOOL. OHALL. EXP,—PART x.—1881.) K 18

138 THE VOYAGE OF H.M.S. CHALLENGER.

to study the formation of the germ-layers, nor the modifications which they undergo
during development. Whether all the cells of the embryo in this stage are derived
exclusively from the blastoderm, or whether they are also partly due to the deutoplasm is
a question which it is impossible to answer from the section before me. Dorsally the
greater part of the embryo is covered by a single row of flattened cells (the original
blastoderm cells), ventrally a plate is clearly distinguished much thicker than the blasto-
derm, and doubtless formed of cells more than one row deep. Unfortunately, however,
the limits of these cells were quite gone; I therefore could not distinguish either their
number or arrangement, but I believe the evidence is great that in the inner layer of this
plate the original mesoblast is to be seen. In this stage rudiments of the appendages
are distinctly formed ; and I consider it a very characteristic feature in the development
of the Pyenogonids, that the food-yolk penetrates into these appendages. In the section
here figured, however, that part of the food-yolk which penetrates the leg, is not in direct
connection with the central food-yolk mass ; but this is caused by the circumstance, that
the section does not pass exactly vertically through the embryo, but goes a little obliquely
from above backwards to the ventral side.

The blastoderm shows to a considerable extent in the stage I have figured a double cell-
layer dorsally in the middle, and even a small lumen is observed between these two.
Small cells or nuclei seem to be present in this lumen, and the whole arrangement made
me think it possible that I had an early stage in the development of the heart before
me. The broad and flattened condition of the heart in the adult animal of Nymphon
is not opposed to this suggestion ; yet it is difficult to understand why a heart should be
developed before there seems to be any question of an intestinal tract.

About the same stage is also figured in figs. 9 and 10. At the ventral side the
first pair of appendages (the foot-jaws), three pairs of legs, between the foot-jaws
the proboscis, and the caudal protuberance, are easily distinguished. The second
and third pair of cephalic appendages show in this species a remarkable retardation
in their appearance, visible in the stage in which the first and second pair of true
legs are already two-jointed and bent inwards so as to meet in the middle of the
ventral surface, and in which the third pair is longer, yet bent inwards and forwards.
In this same stage the third cephalic appendage is not yet distinguishable, and the
second pair only shows a small protuberance at the base of the foot-jaws. An equatorial
section of an embryo in this same stage is figured in fig. 11. Between the foot-jaws (a)
and the first true leg (b) two small protuberances are distinguished, the first of which (c)_
is larger than the second (d), which in this stage is observed only interiorly. The
section is also remarkable for the distinctness with which the nerve ganglia are seen.

There is good reason to consider this arrangement characteristic for the species
Nymphon brevicaudatum, Miers. Other species of Nymphon, of course, may show
the same; so far as I could ascertain it is not the rule, for neither NMymphon

REPORT ON THE PYCNOGONIDA. 139

brachyrhynchus nor N. brevicollum nor N. hamatum agree with N. brevicaudatum
in this regard. Fig. 8 shows a stage in the development of Nymphon brachyrhynchus,
in which the three first pairs of embryonic appendages are already present. The first
pair (the largest) are armed with pincers; the second and third are small, armed with
curved hooks and not taking parts of the food-yolk ; of the true legs in this stage nothing
as yet is to be seen. In figs. 12 and 13 I have figured a larva of Nymphon brevicollum
showing the three cephalic appendages, the first pair of true legs almost completely
developed, the second pair much shorter than the first, and not yet furnished with claws,
the third only as a rudimentary process ; the fourth pair is totally wanting in this stage.
Consequently I believe it is the rule in Nymphon, that the three pair of cephalic
appendages are developed first of all, the legs appearing afterwards in regular succession.

To return to Nymphon brevicaudatum, Miers, in figs. 9 and 10, I have figured embryos
within the shell of the egg almost of the same stage ; with this difference only, that in
fig. 10 the egg is figured as seen from the ventral surface. In fig. 9 also, a part
of the dorsal surface being bent over to the ventral side has been drawn. In this
last figure it is clearly shown that the dorsal surface of the embryo is at least at the
anterior side lined with a shell-like thickening, the proboscis and the first pair of cephalic
appendages being at their origin covered by this thickening as by a cap. Near the
anterior side of this cap the double supra-cesophageal ganglion is situated, making it
evident that in the border of this cap the anterior margin of the cephalic part of the
embryo is to be seen; the proboscis being only an azygous excrescence of that part of
the ventral surface which surrounds the mouth.

The equatorial section figured in fig. 11 shows the distribution of the nerve ganglia
on the ventral surface ; the first and second ganglia are smaller and are placed close to
each other ; the development of the third, fourth, and fifth ganglia is in near relation with
that of the corresponding legs; finally, neither the sixth ganglion nor the fourth pair of
legs is to be distinguished, In the middle the two halves of every ganglion are placed
close to each other, which, as far as I could ascertain, is also the case in earlier stages,
Of the longitudinal commissures between the ganglia in this stage, nothing as yet is to be
distinguished, and as to the cellular structure of the ganglia, I was only able to trace
large cells without any differentiation.

The degree of development the larvee have reached when leaving the shell of the egg
is not the same for all the species of Nymphon ; so I think it probable that the larva of
Nymphon brevicaudatum, Miers, does not creep out of the egg before the four true legs
are developed, whereas the young of Nymphon brevicollum cling to the ovigerous legs
of the father as soon as only one of the pairs of true legs has reached its full development,
and perhaps even earlier yet. So, when Semper affirms that there occurs a complete
metamorphosis in the development of the species of the genus Nymphon, two points
are to be borne in mind, (1) that this does not affect all the species of Nymphon in

140 THE VOYAGE OF H.M.S. CHALLENGER.

the same way, and (2) that here the word metamorphosis has quite a different meaning
from what it has in entomology.

Of the genus Nymphon I was able to compare the larve of the species Nymphon
brevicollum, N. hamatum, and N. longicoxa. Of Nymphon brevicollum 1 have figured
the youngest stage observed in figs. 12 and 13; an older one, which has three pairs of
legs fully developed and the fourth already planned in the form of two lateral processes,
has been drawn from the ventral side in fig. 1 of Plate XX.

On the ovigerous legs of the same animal I found together larve in both the stages I
have figured, and also in intermediate stages. Taking a small number of these larvee from
the leg to study them under the microscope, I often observed the membranes of earlier stages
between them. These membranes, and especially the parts which belong to the fore-part
of the body, are attached to one another by means of long threads; these threads take
their origin in the first joint of the foot-jaw, which bears a protuberance perforated by
the thread. In the interior of the joint, and also of the empty membrane of this joint
the thread can be traced a short way, but in neither to a great extent, as in the joint it
is covered by the food-yolk, and in the membrane soon ceases after having passed the
protuberance.

The larvee of Nymphon hamatum which I was able to study were already furnished
with four legs. Their condition was not extremely favourable for minute investigation,
especially because the food-yolk makes the whole body opaque. The third pair of
cephalic appendages are but small, and have each the form of a two-jointed stump bearing
a pair of small spines at the extremity. The fore-part of the body of this larva is figured
in fig. 3, Plate XX. An apparatus of a very singular shape, and, of course, closely connected
with the protuberance perforated by the long thread in the larva of Nymphon brevicollum,
is situated as in that species in the first joint of the foot-jaw. Numerous bottle-shaped
sacs are placed near each other, and in such a way that their necks meet in one point.
Each neck terminates in a small semilunar border, which covers a small slit; through
this slit a thread passes, that can be easily observed as it runs through the throat of the
bottle-shaped sac. The widened part of the bottle has in its interior two or more
vesicles, which seem to be filled with an opaque protoplasm, covering in all probability
the origin of the thread. Every bottle has its own thread, and of these more than ten
are easily counted. I have figured this apparatus in fig. 4, Plate XX. The study of the
apparatus is very difficult, as it is not transparent, being covered at one side by the food-
yolk. The different bottle-shaped sacs are enclosed in a granular mass, with which
very fine fibres seem to correspond. I could follow these fibres to a certain distance
from the apparatus, where,they are covered by the food-yolk; and from their pale
appearance, and the circumstance that they are not easily coloured by picrocarmine (as
the muscles, fig. 4, are), I felt inclined to look upon them as nerve-fibres.

The same organ, but of a somewhat different shape, occurs also in the mandibles of

REPORT ON THE PYCNOGONIDA. 141

the larvee of Nymphon longicova. These larve in almost every detail correspond with
those of Nymphon hamatum, but the organ here in question is a curious exception.
Ihave figured it in fig. 5 of Plate XX. Numerous small vesicles are in close relation
with each other, and are so placed that they seem to radiate from a common centre. The
whole apparatus is small; fig. 5 shows a drawing enlarged 270 times. The vesicle
corresponds in all probability with a larger one placed in the centre, sending forth the
thread, which in this species is always a single one. The thread is a little swollen at
the foot, and seems (to judge from the double lining under the skin) to run through a
sheath, at the end of which a semilunar border covers a small slit, through which the
thread passes. Of course the chitinous skin of the larva is not coloured by the
picrocarmine, but the broad and flat thread is. This thread is very long, its length
sometimes equalling and even surpassing half the length of the larva; at a certain
distance from the beginning I repeatedly observed a small part of the old skin, which
remained in relation with the thread, while the larva got a new one.

A similar apparatus to the one described by me for the larvee of Nymphon hamatum
and Nymphon longicoxa (and occurring in all probability also in Nymphon brevicollwm) has
been observed by Dohrn in the larva of Achelia. The first joint of the mandible bears a
strong spine in the larva. “ An diesem letzteren sieht man fast immer einen sehr feinen
Faden befestigt und erkennt bei naherer Untersuchung, dass dieser Faden aus dem Dorn
herauskommt. Der Dorn ist nimlich hohl, seine Spitze durchbohrt und im Inneren
sieht man einen zweiten feinen Canal der von einem merkwiirdig gestalteten Organ
ausgeht, das in der Basis des ersten Gliedes der Scheerenfiisse liegt. Das Organ hat
die Gestalt eines Kartenherzens, die Spitze ist verlingert in den eben erwahnten Canal,
der anfiinglich etwas breiter sich bald verschmiilert und quer durch den Innenraum des
Beines sich zu dem Dorn begiebt. Der Canal ist nicht hiutig, sondern hornig, dennoch
beugt er sich in massiger Kriimmung, ehe er den Dorn erreicht. Die Structur der
Driise—denn fiir eine solehe muss ich das sonderbare Organ halten—habe ich nicht
ermitteln konnen, nur so viel vermag ich anzugeben, dass die hintere Hilfte aus kleinen
Zellen bestand, die dem Organ eine gewisse Aehnlichkeit mit einem Nervenganglion ver-
lichen, wiihrend die vordere Hilfte von zwei merkwiirdigen blassen Flecken eingenommen
wurde, die Kugelgestalt besitzen, aber nicht erkennen liessen, ob sie mit irgend einer
Substanz gefiillt waren, oder Hohlkugeln darstellten. Ueber und unter dieser Driise
legen Muskeln, welche zur Bewegung des zweiten Gliedes der Extremitit dienen,” !

There remains no doubt that the organ of Dohrn is the same as that observed by me.
Also, as I already said above, I feel very much inclined to adopt the conjecture about the
character of the organ proposed by him. ‘The organ is a gland, and the product of its
secretion consists of one or more fine threads. These threads occur only in the larval con-
dition, and as for their use I wish to compare them with the byssus threads of the Lamelli-

J Dohrn, J. c., p. 141.

142 THE VOYAGE OF H.M.S. CHALLENGER.

branchiata. The larvee of different species, as observed by me, usually remain for a
long time after having cast off their exuvie, in relation to the ovigerous leg of their
parent. As long as they were enclosed in their egg, they clung together tightly enough ;
but once crept out of the egg-shell, a special arrangement is necessary to keep them
together. This is found in the threads, and the supposed glands from which these take
their origin, as observed by Dohrn and me. Repeatedly I saw, as I have mentioned
already before, between the larvee of Mymphon brevicollum, collections of very numerous
skins held together by means of the threads, and small parts of such a cast skin I found
also in relation with the thread of the larvee of Nymphon longicoxa.

It is true that the structure of the apparatus, as it shows itself in the larva of Nym-
phon hamatum, argues, perhaps, for the conjecture that the organ is an organ of sense,
but then it is exceedingly strange that such an organ should only be found within the
larvee. And it would be difficult to explain the meaning of the single or numerous long
threads as being sent forth from an organ of sense, whereas in relation with a gland their
function can easily be understood.

The study of this same organ which I made last summer in the laboratory of Prof.
Lacaze-Duthiers, at Roscoff, has also convinced me, that my original supposition as to the
function of these organs was erroneous. The fine threads, which I observed in the
interior of the mandible running towards the organ are threads of connective tissue ;
their function is, no doubt, to hold the organ in its place. The young of Nymphon
robustum, Bell, and those of Nymphon brevicaudatum, Miers, are a great deal more
developed when creeping out of the egg than those of Nymphon hamatum, N. longicoxa, and
N. brevicollum. Most probably this spinneret of the larva does not occur in these species.

Besides the larvee of the genus Nymphon, the only other genus of which I could
investigate the larvee was Ascorhynchus. About their development and metamorphosis
nothing as yet has been published. I can only give a drawing of the single larval
stage which I observed, and which is furnished with three pairs of legs. The fig. 6
on Plate XX. shows that the larva in this stage corresponds with larvee of other genera,
as observed by Kroyer, Dohrn, and myself. Of the glands in the foot-jaw no trace
could be discovered; but then the larvee are very small, and their condition is not very good.

8. In studying the anatomy of the Pyenogonids of the Challenger Expedition, I met
with two different kinds of bodies of which I have not been able to ascertain whether they
really belong to the organisation of the Pycnogonids, or must be considered as parasites.
However, I feel much inclined to adopt the latter opinion; and although some doubt
remains, I wish to give a short description of what I have seen, which may, perhaps,
be of use for later investigators.

In the first place I met with some curiously shaped forms in the interior of the body and
of the legs of two different species of Nymphon. I observed them in Nymphon longicoxa
and in Nymphon brevicaudatum, but only in some of the specimens which belonged to

REPORT ON THE PYCNOGONIDA. 143

the male as well as to the female sex. They are comparatively large, often long ovate
cells with a thin wall, the contents consisting of large granules and a longitudinal slightly
curved nucleus.

When colouring the preparations with picrocarmine these forms assume a yellow colour,
the nucleus becoming beautifully red. They seem to be distributed through the body very
irregularly and seem to penetrate all the cavities accessible to the blood. In Nymphon
brevicaudatwm I even observed them in the space before occupied by the eggs, and in
which still an unripe egg was to be seen. Both in this species and in Nymphon longicoxa
most of these curious forms are very regularly placed against the wall of the leg, where
they often form two or even more distinct layers. Their size varies between 0:066 and
0°081 mm. With regard to their nature my opinion is not at all a settled one; but I
am strongly inclined to believe them to be the eggs of some parasitic animal. But what
kind of animal their parent in that case will prove to be I am unable to say.

The other kind of bodies must be regarded, I believe, as ectoparasites of Colossendeis
leptorhynchus. Of the ten specimens of this species in the Challenger collection there are
three which are sprinkled over with these. The one isa male, the two others are female.

They are rounded, sac-forming bodies, often with a crumpled surface placed at the end
of a short stalk, the end of the stalk is in connection with the integument of the Pyecno-
gonid. Their wall is chitinous, and under this outer wall there is a much thinner inner
one ; in the stalk this inner wall is close to the outer one, but in the globular part there
is a large open space between the outer and the much smaller inner sac. In this space
pressed against the outer sac numerous eggs are found, the size of which is 0°088 mm.,
they have a very thin wall and are furnished with a yelk of large rounded elements,
coloured yellow by picrocarmine. A small nucleus as a red coloured spot, however, is
always present.

Whether these are really eggs is the first question to be answered, and I think there
can be no doubt in respect to this. Moreover, to judge from their structure and that
of the capsules, they are eggs that are laid after having been fecundated. There is
only one consideration, I believe, that may be set against this suggestion, and this is,
that all these eggs are in the same state of development; not only those of the same
capsule, but of all the capsules I investigated. It must be borne in mind, however, that
these were brought up by the same haul of the trawl, and probably lived in the neigh-
bourhood of one another ; consequently I think this objection is of no importance.

The second question is whether they are the eggs of that Pycnogonid on the legs of
which they are found, or of another specimen of the same species, or of any other animal.
Of course it is possible that the eggs are Colossendeis eggs; however, I do not think
this very probable. In the first place, because males and females both are studded with
these capsules, and in the second place, because these capsules are totally different from
the ege-masses commonly found on the ovigerous legs of the Pyenogonids. In favour of

144 THE VOYAGE OF H.M.S. CHALLENGER,

this opinion may be advanced that—at any rate as far as | know—hitherto no specimen
of one of the known species of Colossendeis has been caught with egg-masses on its
ovigerous legs. Considering that they are not the eggs of the Colossendeis itself, it
becomes almost impossible to form an opinion as to the animal they belong to. Among
the gastropodous molluscs numerous forms are known, which construct egg-capsules, and
attach them to foreign bodies. Perhaps the present capsules belong to an animal of that
group. That the long legs of our animals may easily be mistaken by other animals for
dead bodies is shown, I believe, by the fact that numerous other animals, which cannot be
considered as parasites, and which, as a rule, are found on stones, shells of molluscs,
carapaces of crabs, &c., fix themselves on these legs. So a small sponge and a poly-
zoon are on Nymphon brachyrhynchus, a stalk-like process most probably of a tubularian
polyp is found on the leg of a Colossendeis ; a species of Scalpellum is extremely numerous
on the legs of Nymphon robustum, Bell. Of the numerous specimens of this species col-
lected in Barents Sea, which I have investigated, there is not a single one with these
ectoparasites. But on the other hand, they are very common on the hundreds of speci-
mens of this species which were obtained by the “ Knight-Errant.” Professor G. O. Sars
enumerates in his two latest papers on the Crustaceans of the Norwegian Expeditions
numerous species of Scalpellum, found at higher northern latitudes, but he does not
mention that they are found on the legs of the most common Pyecnogonid of the North
Atlantic and North Polar Sea. Moreover, a preliminary comparison of this species of
Scalpellum shows differences with those described. I therefore believe it to be a new
one, and wish to name it Scalpellwm nymphocola.

SUMMARY OF THE REPORT.

1. Of the forty-one species of Pycnogonida dredged during the voyage of H.MLS.
Challenger and the cruise of the “ Knight-Errant” thirty-three are new to science.

2, Of the nine genera represented in those collections three are new.

3. Those genera which range most widely geographically are also those which range
most widely in depth,

4. There are deep-sea species, but true deep-sea genera do not scem to exist.

5. The Pyenogonida form a distinct and very natural group (class) of arthropodous
animals, Their common progenitor (their typical form) must be considered as a hypo-
thetical Pycnogonid with three-joited mandibles, multi-jointed palpi, and ovigerous legs
with numerous rows of denticulate spines on the last joints.

6. This class of the Arthropoda may be thus characterised :—Arthropoda breathing by
the general surface of the body, which body consists of a cephalothoracic, three thoracic
segments, and a rudimentary abdominal segment. The cephalic part of the cephalothoracic
segment bears anteriorly a proboscis, consisting of three coalesced parts, one pra-oral
(labrum ?), two post-oral ones (mandibles ?), and three pair of cephalic appendages, the
first two of which in the adult state sometimes have become rudimentary, the third pair
being always present at least in one of the two sexes. The first pair of these appendages
represents the antenn, the two others are post-oral. The thoracic part of the cephalo-
thoracic segment and the three thoracic segments are each furnished with a pair of long
eight-jointed legs, into which the alimentary canal sends off long cceca.

7. The function of the integumentary cavities is primarily respiratory.

8. The typical form of the nervous system shows a supracesophageal and five
thoracic ganglia. The supracesophageal ganglion gives off the nerves for the mandibles
(antennee), the integumentary nerves, and a strong nerve for the proboscis. Besides these
it probably gives off nerves for the intestine (sympathic nerves). The first thoracic
ganglion consists of two coalesced ganglia, and gives off four pairs of nerves, two pairs
innervating the proboscis, then the pair of palpar nerves, and finally those for the ovi-
gerous legs, The following four ganglia give off the nerves for the four pairs of legs ; the
last ganglion gives sometimes two sometimes one pair of nerves for the abdomen.

9. In addition to the nerves mentioned above the proboscis is innervated by three
strong bundles of nerves and ganglia united by a stronger and some feebler secondary
cesophageal nerve rings.

(ZOOL. CHALL, EXP,—PART x.—1881.) ~ K 19

146 THE VOYAGE OF H.M.S. CHALLENGER.

10. In some genera the inner surface of the integument is covered by a net-work of
nerves and ganglia in connection with, and most probably issuing from, the integu-
mentary nerves given off by the supracesophageal ganglion,

11. In the most primitive condition the eye of the Pyenogonid consists of a rounded
transparent part of the integument, the inner surface of which is furnished with some
small ganglia and nerve-fibres issuing from the integumentary nerve bundle. The highly
developed eye of the shallow-water species shows ganglionic cells, distinct retinal rods,
and a lens consisting of a thickened part of the chitinous skin of the animal.

12. Those eyes which have lost their pigment and their retinal rods are rudimentary.
They cannot be considered as forming the transition between the highly-developed eye
and its most primitive condition.

13. That part of the cesophagus which runs through the proboscis has the function of
a masticating apparatus. Where the cesophagus enters the intestinal tract (the stomach)
small glands (pancreatic, most probably) are present.

14. The original condition of the genital glands is in the form of a U-shaped mass,
placed above the intestine and giving off branches which penetrate the legs. Whereas for
the male glands the original form prevails in most (all ?) genera, for the female glands it
seems to be a rule that only the lateral parts entering the legs are developed. The genital
pores of the females are larger than those of the males ; they are found ventrally towards
the extremity of the second joint of the leg. Whereas for the females it is the rule that
these pores are present on all the legs; it often happens in the males that they are only
present on the two or three hindmost pair of legs.

15. There are always distinct vasa efferentia, but there are not always true oviducts.

16. In Nymphon brevicaudatum, Miers, females also bear the eggs on the ovigerous legs.

17. The larva creeping out of the egg is already furnished with an azygous outgrowth
of the region surrounding the mouth (the proboscis). Asa rule in that stage only three
pairs of appendages (the later cephalic ones) are present.

18. These larvee are often furnished on their mandibles with an apparatus producing a
single or numerous threads, wherewith the young is attached to the ovigerous leg of its
parent.

19. About the relation in which the Pycnogonida stand to either the Crustacea or
the Arachnida we know as much or as little as we do about the relation in which these
two classes Arthropoda stand to each other.

Note.—While I was engaged in preparing the index of this report, and after the
rest of it had been printed off, Mr Edmund B. Wilson of Baltimore kindly sent me two
papers which he had recently published. In one (the Pycnogonida of New England and
Adjacent Waters, Report of the United States Commissioner of Fish and Fisheries, part
vi. for 1878, pp. 463-506, pls. i—vii.) the author gives an account of the present know-

REPORT ON THE PYCNOGONIDA. 147

ledge of the species of Pycnogonida known to occur on the coasts of New England and
Nova Scotia. With two exceptions (Achelia scabra, Wilson, and Nymphon macrum,
Wilson) the species here described are the same as those of a former paper by Mr Wilson,
published in the Trans. Connect. Acad. Sci., vol. v. pp. 1-26, 1880. The new Achehia
is quite unknown to me, but MVymphon macrum, Wils., is undoubtedly the species
which I have described in my report (p. 45) as Nymphon brevicollum. The Challenger
specimens were taken south of Halifax (83 fathoms), those described by Mr Wilson
in the Gulf of Maine (85 to 115 fathoms).

The other paper (Reports on the Results of Dredging, under the Supervision of
Alexander Agassiz, along the East Coast of the United States, during the summer of 1880,
by the United States’ Coast Survey Steamer “ Blake,” Commander J. R. Bartlett, U.S.N.,
commanding. xiii. Report on the Pyenogonida, by Edmund B. Wilson; Bulletin of
the Museum of Comparative Zodlogy at Harvard College, vol. viii., No. 12, Cambridge,
Mass., March 1881, pp. 239-256, pls. i—v.) contains descriptions of ten species of Pyeno-
gonids, five of which are new. These belong to three genera, two of which are con-
sidered by the author as new. The new species are in the first place two species of
Colossendeis, Jarzynsky, Colossendeis colossea, and Colussendeis macerrima. Then a
new genus Scaeorhynchus, with the species Scweorhynchus armatus, is proposed ; finally,
the new genus Pallenopsis, with the species Pallenopsis forficifer and Pallenopsis
longurostris, is described. The descriptions are illustrated by very good figures. On
comparing these figures and descriptions with those of my report, there can be little
doubt that Colossendeis colossea and C. macerrima are very nearly related to, if not
identical with, my Colossendeis gigas and C. leptorhynchus. As to the genus Scaeo-
rhynchus, 1 do not think there are sufficient grounds for separating it from Ascorhynchus,
G. O. Sars. Neither the presence of dactyli on the first pair of legs, nor the structure
of the rudimentary mandibles (antennae) makes it proper to separate these genera:
Scacorhynchus (like Gnamptorhynchus, Bohm) is only a synonym of Ascorhynchus.
The species armatus, Wilson, seems to be different from those hitherto described, and
also from those of the present report.

The new genus Pallenopsis is intended to embrace those species which come near to
Phoxichilidium, but which are characterised by ten-jointed accessory legs present in both
sexes, and by three-jointed mandibles. Three (perhaps four) species described in my
report show these characters also, and (pp. 82 and 88) I have been long in doubt whether
I should not propose a new genus for these species. I did not take the step because I do
not wish to augment the number of genera more than necessary until our knowledge
of generical characters is more perfect. Mr Wilson is not so slow in proposing new
genera ; in the present instance, I believe, however, that his proposal has a fair chance of
being accepted. The two species described by Mr Wilson are, I believe, different from
those described in my report.

148 THE VOYAGE OF H.M.S. CHALLENGER,

I regret very much that in my report species will be found mentioned, described, and
figured as new, which at the date of its publication will have been already described.
As I was aware of the large collections of deep-sea animals collected by Professor
Alexander Agassiz, and felt sure that my report, with its numerous plates, would take
- a considerable time in passing through the press, I took the liberty of writing to
Professor Agassiz, to ask him to whom the working-out of the Pyenogonids of his latest
cruises had been entrusted. He kindly complied with my request, and informed me that
the Pyenogonids along with the Crustacea had been sent to Professor Alphonse Milne-
Edwards in Paris. I then addressed Professor Milne-Edwards, sending him at the same
time proof-copies of the plates of my report on which the new species were figured, and
as he favoured me with an answer, in which he promised to make use of the names
proposed by me, I had every reason to believe that zoological literature, at least in the
case of the deep-sea Pycnogonida, would not be encumbered by synonyms. Where I
have not been successful in this respect I hope nobody will lay the blame upon me.

LEIDEN, 19th May 1881.

EXPLANATION OF PLATES,

PLATE I.

Nymphon hamatum, n. sp. (figs. 1-9).

. Male, dorsal view ; magnified 3 diameters.

Male, ventral view ; magnified 7 diameters.

. The claws of the mandibles; magnified 41 diameters.

The last four joints of the ovigerous legs; magnified 34 diameters.

. The denticulate spines of the ovigerous legs; magnified 272 diameters.

The second coxal joint of the leg of a female; magnified 6 diameters.

. The tubercles on the thigh of the male; magnified 94 diameters.

. The hook-like process at the end of the thigh ; magnified 41 diameters.

. The last two joints and the claw of one of the legs ; magnified 21 diameters.

Son dD wa

PLATE II.

Nymphon longicoxa, n. sp. (figs. 1-5).
. Male, dorsal view ; magnified 72 diameters.
. The last four joints of the palpus ; magnified 20 diameters.
The claws of the mandibles ; magnified 94 diameters.
. The denticulate spines of the ovigerous legs ; magnified 272 diameters.
. The last two joints and the claw of one of the legs ; magnified 41 diameters.

ow 0 PO oe

Nymphon compactum, n. sp. (figs. 6-8).

6. Female, ventral view ; magnified 64 diameters.

. Part of the body of a female, dorsal view ; magnified 8 diameters.

. The denticulate spines of the ovigerous legs ; magnified 272 diameters.

Nymphon procerum, un. sp. (figs. 9-12),
. Female, dorsal view ; magnified 6? diameters.
. The claws of the mandibles; magnified 94 diameters.
. The claw of the ovigerous leg; magnified 94 diameters.
The denticulate spines of the ovigerous legs ; magnified 272 diameters.

150 THE VOYAGE OF H.M.S. CHALLENGER.

PLATE III.

Nymphon longicollum, un. sp. (figs. 1-3).

. Male, dorsal view ; magnified 6? diameters.
2. The same, seen ventrally ; magnified 20 diameters.
3. The claws of the mandibles; magnified 47 diameters.

=
ge
—

Nymphon meridionale, n. sp. (figs. 4-8).
4, Male, dorsal view ; magnified 20 diameters.
5. The claws of the mandibles ; magnified 94 diameters.
, 6. Clawand last part of the tenth joint of the ovigerous leg; magnified 272 diameters.
7. The last two joints of the leg; magnified 41 diameters.
8. The claw with one of the secondary claws of one of the legs; magnified 136
diameters.

Nymphon grossipes, Fabr. (sp.), (figs. 9-12).
Called Nymphon armatum, un. sp., at the foot of the plate.

Fig. 9. Male, ventral view ; magnified 6? diameters.

, 10. The claws of the mandibles; magnified 41 diameters.

» 11. The denticulate spines of the ovigerous legs ; magnified 575 diameters.
12. The last joint of the leg of a female ; magnified 41 diameters.

Nymphon brevicollum, nu. sp. (figs. 13-15).

Fig. 13. Female, ventral view ; magnified 67 diameters.
. 14. Claw and last part of the tenth joimt of the ovigerous leg; magnified 272
diameters.
, 15. Claw with one of the secondary claws of the leg; magnified 94 diameters.

PLATE IV.
Nymphon grossipes, Faby. (sp.) (fig. 1).
Called Nymphon armatum, u. sp., at the foot of the plate.

Fic. 1. Oculiferous tubercle ; magnified 41 diameters.

Nymphon brachyrhynchus, nu. sp. (figs. 2-7).
Fig. 2. Male, dorsal view; magnified 41 diameters.

3, Female, ventral view; magnified 6? diameters.

»”

Noone

5
13.

oP © DD Ee

6 ON DS

REPORT ON THE PYCNOGONIDA. 151

. The claws of the mandibles ; magnified 94 diameters.
. Palpus; magnified 41 diameters,

. Claw of the ovigerous leg ; magnified 272 diameters,
. Claw of one of the legs; magnified 94 diameters,

Nymphon fuscum, n. sp. (figs. 8-11).

. Male, ventral view; magnified 63 diameters.

. The claws of the mandibles; magnified 94 diameters.
10.
vale

Palpus ; magnified 41 diameters.
Claw of the ovigerous leg ; magnified 180 diameters.

Nymphon brevicaudatum, Miers (figs. 12-13).
Called Nymphon hispidum, n. sp., at the foot of the plate.

Male, dorsal view; magnified 12 diameters.
Male, ventral view ; magnified 6 diameters.
PLATE V.

Nymphon brevicaudatum, Miers (figs. 1-5).
Called Nymphon hispidum, n. sp., at the foot of the plate.

. Palpus; magnified 41 diameters.

. Claws of the mandibles; magnified 41 diameters.

. Last five joints of the ovigerous leg ; magnified 41 diameters.

. Denticulate spine of the ovigerous leg ; magnified 272 diameters
. Last two joints of the leg; magnified 34 diameters.

Nymphon perlucidum, nu. sp. (figs. 6-10).

. The front part of the body, seen ventrally ; magnified 41 diameters.

. The whole animal, dorsal view ; magnified 6? diameters.

. The last four joints of the ovigerous legs; magnified 94 diameters.

. Two of the denticulate spines of the ovigercus leg; magnified 272 diameters.
. The last two joints of the leg ; magnified 36 diameters.

Ascorhynchus orthorhynchus, n. sp. (figs. 11-13).

. Dorsal view; magnified 34 diameters.

Ventral view; magnified 2 diameters.
Palpus ; magnified 21 diameters.

152

© COND oO

10.

ot
12.
13.
14.
15.
16.

of WN

THE VOYAGE OF H.M.S, CHALLENGER.

PLATE VI.

Ascorhynchus orthorhynchus, nu. sp. (figs. 1-4).

. Rudimentary mandible ; magnified 94 diameters.
. The last four joints of the ovigerous leg ; magnified 21 dianicters.
. The denticulate spines of one of the joints of the ovigerous leg ; magnified 272

diameters.

. The last two joints of the leg; magnified 21 diameters.

Ascorhynchus glaber, n. sp. (figs. 5-9).

. Dorsal view ; magnified 54 diameters.

Mandibles ; magnified 21 diameters.

. The mandible of a young specimen; magnified 94 diameters.
. The last four joints of the ovigerous leg; magnified 21 diameters.
. The last joint of the leg; magnified 21 diameters.

Ascorhynchus minutus, n. sp. (figs. 10-16).

Ventral view ; magnified 74 diameters.

Side view ; magnified 72 diameters.

The last three joints of the ovigerous leg ; magnified 70 diameters.
The eighth joint of the ovigerous leg ; magnified 182 diameters.
The last two joints of the leg ; magnified 70 diameters.

The last joint of the first leg; magnified 94 diameters.

Hairs of the palpus; magnified 272 diameters.

PLATE VII.

Oorhynchus aucklandie, n, sp. (figs. 1-7).

. Ventral view; magnified 15 diameters.

. Dorsal view ; magnified 74 diameters.

. The front part seen dorsally ; magnified 34 diameters. |

. Palpus; magnified 94 diameters.

. The last four joints of the ovigerous leg ; magnified 130 diameters.
. One of the legs; magnified 34 diameters.

. The last two joints of the leg; magnified 70 diameters.

” 10
pp all
” 12

Fig. 3
”» t
» 9
» 6
ay od

Hig. 1
» 3

Fig. 4

Vig. 6
pat
» 8

(ZOOL. CHALL, EXP.—PaRT x.—1881.)

REPORT ON THE PYCNOGONIDA. 153

Discoarachne brevipes, n. sp. (figs. 8-12).

. Dorsal view; magnified 8 diameters.

. Ventral view ; magnified 8 diameters.

. Palpus; magnified 94 diameters,

- The last four joints of the ovigerous leg ; magnified 94 diameters,
. The last two joints of the leg ; qiecoifet 94 diameters.

PLATE VIII.

Colossendeis gigas, n. sp. (figs. 1-2).

. Ventral view; natural size,
2. Dorsal view of the body ; natural size.

Colossendeis leptorhynchus, n. sp. (figs. 3-7).

. Ventral view ; natural size.

. Dorsal view of the body ; natural size.

. The last four joints of the palpus; magnified 30 diameters.

- The last four joints of the ovigerous legs ; magnified 21 diameters.
. The claw of one of the legs ; magnified 48 diameters.

PLATE IX.

Colossendeis megalonyzx, n. sp. (figs. 1-3).

. Lateral view ; magnified 2 diameters,
2. The last three joints of the palpus ; magnified 39 diameters.
. The arrangement of the denticulate spines on the ninth one of the ovigerous

leg ; magnified 94 diameters.

Colossendeis robusta, n. sp. (figs. 4, 5).

. Dorsal view ; magnified 2 diameters.
5. The arrangement of the denticulate spines on the ninth joint of the ovigerous

leg ; magnified 41 diameters.

Colossendeis gracilis, n. sp. (figs. 6-8).

. Ventral view ; magnified 5 diameters.
. The last four joints of the palpus; magnified 41 diameters.
. The arrangement of the denticulate spines on the ninth joint of the ovigerous

leg ; magnified 235 diameters.
K 20

154

Fig.

ue

THE VOYAGE OF H.M.S. CHALLENGER.

PLATE X.

Colossendeis gigas, n. sp. (figs. 1-5).
The arrangement of the denticulate spines at the ninth joint of the ovigerous
oD J oO

leo ; magnified 41 diameters.

. One of the denticulate spines of the ninth joint of the ovigerous leg of an old

specimen ; magnified 136 diameters.

. The same of an outside row of a younger specimen ; magnified 136 diameters.
. The same of an inside row of a younger specimen ; magnified 136 diameters.
. Two rudimentary spines of a row quite to the inside of an old specimen ; magni-

fied 136 diameters.

Colossendeis gracilis, n. sp. (figs. 6-7).

. Specimen with mandibles, dorsal view ; magnified 63 diameters.
. The arrangement of the denticulate spines on the ninth joint of the ovigerous

leo; magnified 94 diameters.

Colossendeis brevipes, n. sp. (figs. 8-9).

. The last five joints of the palpus; magnified 20 diameters.

9. The arrangement of the denticulate spines on the ninth joint of the ovigerous

leo ; magnified 94 diameters.

Colossendeis minuta, n. sp. (figs. 12-14).

. Dorsal view ; magnified 6 diameters,
. The last five joints of the palpus; magnified 41 diameters.
. The arrangement of the denticulate spines on the ninth joint of the ovigerous

leg; magnified 272 diameters.

PLATE XI.

Pallene australiensis, n. sp. (figs. 1-7).

. Ventral view ; magnified 7 diameters.

. Dorsal view ; magnified 17 diameters.

. Claws of the mandibles; magnified 94 diameters.

. Last five joints of the ovigerous leg of the male ; magnified 34 diameters,
. Ninth joint of the ovigerous leg of the male ; magnified 270 diameters,

. Last two joints of the leg; magnified 65 diameters.

. Spine on the sixth joint of the leg; magnified 270 diameters.

Fig.

a

Sri

CONS

10.

REPORT ON THE PYCNOGONIDA. 155

Pallene levis, n. sp. (figs. 8-12).

. Female specimen, dorsal view ; magnified 6 diameters,
. Female specimen, ventral view ; magnified 17 diameters,
. Last four joints of the ovigerous leg ; magnified 65 diameters,

Last joint of the ovigerous leg; magnified 272 diameters.

. Last two joints of the leg; magnified 41 diameters.

oO?

PLATE XII.

Pallene languida, n. sp. (figs. 1-5).

Ventral view ; magnified 41 diameters.

. Dorsal view ; magnified 41 diameters,

Last joint of the mandible ; magnified 94 diameters,
Last five joints of the ovigerous leg ; magnified 94 diameters,
Denticulate spines of the ovigerous leg ; magnified 575 diameters,

Phowichilidium patagonicum, n. sp. (figs. 6-9),

Dorsal view, natural size.

Ventral view ; magnified 6 diameters,

Last four joints of the ovigerous leg; magnified 36 diameters.
Last two joints of the lee; magnified 6 diameters.

Phoxichilidium patagonicum, vay. elegans, Hoek (fig. 10).

Ventral view ; magnified 8 diameters,

PLATE XIII.
Phoxichilidium oscitans, n. sp. (figs. 1-5).

Dorsal view ; magnified 4 diameters.

Front part of the body, seen ventrally ; magnified 8 diameters.
The mouth seen from the front ; magnified 7 diameters.

Last four joints of the ovigerous leg; magnified 41 diameters.
Last two joints of the leg ; magnified 8 diameters.

Phoxichilidium mollissimum, n. sp. (figs. 6-9).

Lateral view ; magnified 4 diameters.
Mouth, front view ; magnified 9 diameters.

= wn

THE VOYAGE OF H.M.S. CHALLENGER.

. Last four joints of the ovigerous leg ; magnified 28 diameters.
. Part of the sixth joint of the leg; magnified 8 diameters.

Phoxichilidium pilosum, n. sp. (figs. 10-13).

. Dorsal view ; magnified 5 diameters.

. Front part of the body, ventral view ; magnified 9 diameters.
. Last four joints of the ovigerous leg ; magnified 41 diameters.
. Last two joints of the leg ; magnified 9 diameters.

PLATE XIV.

Phowichilidium fluminense, Kroyer (figs. 1-4).

. Ventral view ; magnified 8 diameters.

. Oculiferous tubercle, dorsal view ; magnified 28 diameters.

. Last five joints of the ovigerous leg ; magnified 56 diameters.
. Last two joints of the leg; magnified 28 diameters.

Phoxichilidium insigne, n. sp. (figs. 5-7).

Dorsal view ; magnified 8} diameters.

6. Front part of the body, seen ventrally ; magnified 28 diameters.

. Last two joints of the leg; magnified 56 diameters.

Hannonia typica, nu. gen., n. sp. (figs. 8-11).

. Dorsal view ; magnified 17 diameters.
. Ventral view ; magnified 53 diameters.
10.
MA

Last four joints of the ovigerous leg ; magnified 70 diameters.
Last two joints of the leg; magnified 30 diameters.
PLATE XV.

Nymphon macronyx, G. O. Sars. (figs. 1-7).

Ventral view; magnified 7 diameters.

. Oculiferous tubercle ; magnified 64 diameters.
. Mandible; magnified 41 diameters.

. Palpus; magnified 41 diameters.

. Denticulate spines of the ovigerous legs ; magnified 272 diameters.
. Claw of the ovigerous leg ; magnified 272 diameters.
. Last two joints of the leg; magnified 41 diameters.

BLO:

5 db

ig. 12.

13.

r. 14,
15.

ie. 16.

REPORT ON THE PYCNOGONIDA. 157

Nymphon longicowu, Hoek (figs. 8, 9).

. Spines at the sixth joint of the ovigerous leg of a male; magnified 272 dia-

meters.

. Genital opening of the male ; magnified 136 diameters.

Nymphon conpactum, Hoek (fig. 19).
Last two joints of the leg; magnified 7 diameters.

Nymphon longicollum, Hoek (fig. 11).
Auxiliary claws; magnified 272 diameters.

Nymphon brevicollum, Hoek (figs. 12, 13).

Articulation (?) in the fifth joint of the ovigerous leg of the male; magnified
94 diameters.
The ovigerous leg of the male; magnified 7 diameters.

Ascorhynchus orthorhynchus, Hoek (figs. 14, 15).

Mouth, front view ; magnified 5 diameters.
Genital pore of the female; magnified 64 diameters.

Ascorhynchus gluber, Hoek (fig. 16).

Articulation of the proboscis ; magnified 6 diameters.

PLATE XVI.

Structure of the integument of Nymphon robustwm, Bell (figs. 1-8).

. Transverse section of the integument ; magnified 272 diameters. «a, spine ; b,

respiratory cavity; c, sete; d, nerve; e, blood-corpuscles ; f, epithelium.

. Setze ; magnified 575 diameters.
. Setze; magnified 575 diameters.

Structure of the integument of Mymphonhamatum, Hoek (figs. 4-6).

4. Surface of the fourth joint of the leg of a male ; magnified 94 diameters. g, pores.

. Structure of the gland; magnified 272 diameters.
. Transverse section of the thigh of a male; magnified 94 diameters. g, pore ;

k, blood ; 7, intestinal ccecum ; h, gland.

Structure of the integument of Nymphon brevicaudatum, Miers (fig. 7).

. Transverse section of the fourth joimt of the leg of a female; magnified 56

diameters. 72, as in fig. 6; /, mature egg ; m, immature eggs; x, mud.

158 THE VOYAGE OF H.M.S. CHALLENGER.

Structure of the integument of Ascorhynchus glaber, Hoek (figs. 8-10).

Fig. 8. Transverse section of a part of the integument ; magnified 272 diameters. }, ¢,
e, as in fig. 1.
, 9. Transverse section of the thigh of a male; magnified 56 diameters. 1, testis ;
g, h, i, k, as in fig 6.
, 10. Cells from the glandular mass of the male; magnified 272 diameters.

Genital organs, &e., of Ascorhynchus orthorhynchus, Hoek (fig. 11).

Fig. 11. Transverse section of the thigh of a female ; magnified 56 diameters. k, m, h, 2,
as in figs. 6 and 7.

Structure of the integument of Colossendeis leptorhynchus, Hoek (figs. 12, 18).

Fig. 12. Transverse section of a part of the integument; magnified 170 diameters. 8, e,
as in fig. 1.
, 18. Spine; magnified 170 diameters.

Structure of the integument of Colossendeis megalonyx, Hoek (fig. 14).
Fig. 14. Transverse section through the thigh of a male; magnified 41 diameters. A, 2,
as in fig. 6.
Structure of the integument, &c., of Colossendeis leptorhynchus, Hoek (figs. 15, 16).

Fig. 15. Transverse section through the thigh of a male; magnified 272 diameters. 9,
vesicle ; p, wounded canal.
, 16. Transverse section of the thigh of a female; magnified 56 diameters. m, 7, as
in fig. 7.

Structure of the integument of Phowichilidium patagonicum, Hoek (fig. 17).
Fig. 17. Transverse section of the integument of a female ; magnified 170 diameters. 8, ¢,
J, as in fig. 1.
Structure of the integument, &c., of Phowichilidium insigne, Hoek (fig. 18).
Fig. 18. Transverse section of the thigh of a male; magnified 94 diameters. h, 7, k, as
in fig. 6.
PLATE XVII.

Fig. 1. Colossendeis proboscidea, Sab. (sp.); dorsal half of the body; magnified 6
diameters. «, intestine; a’, a’, two short czeca not reaching beyond the
cephalothorax ; b, muscles moving the proboscis; c, heart; d, anus.

Fig.

Fig.

. Nymphon robustum, Bell ; part of the intestine; magnified 47 diameters. «

REPORT ON THE PYCNOGONIDA. 159

. Colossendeis proboscidea, Sab, (sp.) ; ventral half of the body with the nervous

system ; magnified 6 diameters. a, parts of the intestine 3p, palpus; I. IT.~
V., first to fifth thoracic ganglia ; np. and n.pr., two branches of the palpar
“nerve ; 7.0.1, nerve for the ovigerous leg; n'—n‘, four nerves for the legs ;
n.a., nerves for the abdomen.

. Nymphon robustum, Bell; ventral half with the nervous system ; magnified 6

diameters. a, parts of the intestine, cceca, &c. ; m.U., muscles running from
the one segment to the other; n.p., palpar nerve ; 7.pr., proboscideal nerve ;
n.0.1., n'—n*, na., as in fig. 2.

. Nymphon robustum, Bell; supracesophageal ganglion with its nerves ; magnified

6 diameters, a, intestine ; m, mandibles ; g.s.0., supracesophageal ganglion ;
c, esophageal commissures; n.m., nerve for the mandibles ; w.p.n., unpair
proboscideal nerve; p.p.v., small proboscideal nerves; g.p., proboscideal
ganglion.

. Nymphon robustum, Bell; dorsal half of the body showing the intestine; mac-

nified 4 diameters. a, intestine ; e, cesophagus.

>

intestine ; e, cesophagus ; gl, intestine glands.

PLATE XVIII.

. Integumentary cavities of Colossendeis leptorhynchus, Hoek ; $ specimen ; first

tibial joint; magnified 287 diameters. 7, part of the wall of the intestinal
coecum ; ¢, septa of connective tissue ; b, blood-corpuscles ; d, and d’, glandu-
lar cells.

. Transverse section of the fourth joint of the leg of Colossendeis proboscidea, Sab.

(sp.);_ 3 specimen ; magnified 47 diameters. 7, intestinal coecum ; g, glands;
t, testis; c, fibres of connective tissue.

- Part of the integument of Colossendeis proboscidea, Sab. (sp.) ; fourth joint of

the leg ; 3 specimen ; magnified 272 diameters. ¢, integumentary cavity ; g,
gland; d, duct of the gland,

. GAsophageal ring of Colossendeis megalonyx, Hoek ; magnified 40 diameters.

Ss. supracesophageal ganglion ; c, commissures; ¢, first thoracic ganglion ;
pr. azygous proboscideal nerve ; m, mandibular nerve ; 0, optic nerves (2); ¢’,
first nerve arising from the first thoracic ganglion; ¢”, second nerve (one of
the three main proboscideal nerves), dividing into two branches after pene-
trating the proboscis ; pa., palpar nerve (dividing in two branches close to
the ganglion) ; 0, nerve for the ovigerous leg; c’, commissures between the
first and second thoracic ganglia.

160

THE VOYAGE OF H.M.S. CHALLENGER.

5. Innervation of the rudimentary eyes of Nymphon robustum, Bell; magnified 94
diameters. , optic nerves forming the ganglion g; t, oculiferous tubercle ;
o, rudimentary eyes.

6. Innervation of the proboscis of Nymphon robustum, Bell; magnified 10 dia-
meters. The proboscis has been figured as transparent; the mandible and
the palp of the left side have been cut away. ¢, oculiferous tubercle ; s, supra-
cesophagal ganglion; c, cesophagal commissures; u, azygous proboscideal
nerve; p, secondary proboscideal nerves arising from the supracesophageal
ganglion ; mn, mandibular nerves; p, proboscideal nerves arising from the
first thoracic ganglion; g, ganglionic bundles; «, small ganglia in the front
of the proboscis; y, large proboscideal ganglia; a, first proboscideal nerve
ring ; a@-a! second to fifth proboscideal ring.

7. Transverse section of cephalothoracic segment of Colossendeis leptorhynchus,
Hoek (female specimen) ; magnified 10 diameters. s, supracesophageal gan-
glion ; ¢, first thoracic ganglion ; @, cesophagus ; c, cesophageal commissures ;
2, rudimentary cceca of the intestine ; m, and mm’, muscle-bundles ; m, passing
through the cesophageal commissures.

8. Part of the ganghonie bundle in the proboscis of Nymphon robustum, Bell;
magnified 94 diameters. wu, g, a, a’, a”, x, and y, as in fig. 6.

9, Transverse section of the proboscis of Nymphon robustum, Bell; magnified 23
diameters. I., II., and III. the three chitinous plates limiting the cesophageal
cavity ; t, transverse muscles ; /, longitudinal muscle-bundles ; @, proboscideal
ring; g, ganglion of the ganglionic bundle; p, the three main proboscideal
nerves on transverse section.

10. One of the ganglia on the inner surface of the integument of Colossendeis pro-
boscidea, Sab. (sp.); magnified 272 diameters. c, integumentary cavities ;
b, blood-corpuscles.

11. Six sections through the supracesophageal and first thoracic ganglia of Nym-
phon strémz, Kroyer ; magnified 56 diameters. s, supracesophageal ganglion ;
@, cesophagus; ¢, first thoracic ganglion; 2, intestinal ccecum for the
mandibles; ¢, fibres of connective tissue; 0, optic lobes; 0’, part of the
optic nerves; m, mandibular lohes; x, azygous lobe of unknown function ;
co, esophageal commissures ; p, origin of the two main proboscideal nerves ;
I, origin of the nerves for the ovigerous legs; co’, commissures between the
first and second thoracic ganglia.

12. Longitudinal section through the first thoracic ganglia of Nymphon brachy-
rhynchus, Hoek ; magnified 170 diameters. pv, proboscideal nerves ; pa, part
of the neurilemma of the palpar nerve ; e, part of the neurilemma of the oviger-
ous nerve ; c, commissure between this and the second thoracic ganglion.

REPORT ON THE PYCNOGONIDA. 161

PLATE XIX.
Fig. 1. Ego-mass of Nymphon brevicollum, Hoek : magnified 16 diameters.

» 2. Transverse section of egg-mass of Nymphon brevicollum, Hoek; magnified 41
diameters. 0, opening occupied by the ovigerous leg; s, small pores left
between the eggs ; c, the substance soldering the eges together ; m, mud.

» 3. Transverse section of the egg of Nymphon brevicollum, Hoek ; magnified 272
diameters.

» 4. Structure of the protoplasm of one of the segments of the same ege ; magnified
575 diameters.

» 5. Cells of the blastoderm and segments of the nutritive yolk of Nymphon brevi-
caudatum, Miers ; magnified 272 diameters.

» 6. Nuclei of the cells of the blastoderm of the eggs of Nymphon brevicuudatum,
Miers ; magnified 575 diameters.

» 7. Transverse section through the egg of Nymphon brevicaudatum, Miers ; magni-
fied 94 diameters.

» 8. Embryo of Nymphon brachyrhynchus, Hoek, showing the three pairs of append-
ages and the proboscis ; magnified 94 diameters.

» 9. Front part of the embryo of Mymphon brevicaudatum, Miers, seen ventrally ;
magnified 135 diameters.

,», 10. The embryo of Nymphon brevicuudatum, Miers, ventral view : magnified 94
diameters. :

,», 11. Transverse section through the egg of Mymphon brevicaudatum, Miers:
magnified 94 diameters. a, mandible ; ), first pair of legs ; c, d, second and
third pair of cephalic appendages.

» 12. Larva of Nymphon brevicollum, Hoek, dorsal view ; magnified 94 diameters.

» 13. Larva of Nymphon brevicollum, Hoek, ventral view ; magnified 94 diameters.

PLATE XX.
Fig. 1. Larva of Nymphon brevicollum, Hoek ; magnified 94 diameters.

, 2. Spinning apparatus in the mandible of the larva of Mymphon brevicollum, Hoek :
magnified 94 diameters.

, 38. Front part of the larva of Nymphon hamatum, Hoek ; magnified 94 diameters.

» 4. Spimning apparatus in the mandible of the larva of Nymphon hamatum, Hoek ;
magnified 272 diameters.

, 9. Spinning apparatus in the mandible of Nymphon longicoxa, Hoek ; magnified
272 diameters.

» 6. Larva of Ascorhynchus minutus, Hoek ; magnified 272 diameters.

(ZOOL, CHALL, EXP.—PAKT x.—1881.) K 21
+

162

woe

Wife

18.

THE VOYAGE OF H.M.S. CHALLENGER.

PLATE XXI.

Eye of Nymphon strémi, Kroyer, transverse section ; magnified 272 diameters.
Eye of Nymphon brachyrhynchus, Hoek, longitudinal section, taken laterally ;
magnified 170 diameters.

. Eye of Nymphon brachyrhynchus, Hoek, longitudinal section, passing nearly

through the middle ; magnified 170 diameters.

. Rods and ganglion cells from the eye of Nymphon brachyrhynchus, Hoek ;

magnified 575 diameters.

. Rods (isolated) from the eye of Nymphon brachyrhynchus, Hoek; magnified

575 diameters.

. Gsophagus of Mymphon hamatum, Hoek, transverse section; magnified 272

diameters.

. Glands at the end of the cesophagus of Nymphon hamatum, Hoek ; magnified 94

diameters. a, the glands; s, supracesophageal ganglion; f, first thoracic
ganglion.

. Glands at the end of the cesophagus of Nymphon hamatum, Hoek, transverse

section; magnified 170 diameters. «a, the glands; b, the wall of the in-
testine.

. Group of fat cells from Nymphon robustum, Bell ; magnified 272 diameters.
. Male genital organs of Colossendeis proboscidea, Sab. (sp.), natural size. a,

testis ; b, intestine.

. The opening of the male genital organs in the second joint of the leg of Colos-

sendeis proboscidea, Sab. (sp.). a, testis ; b, intestine ; ¢, vas efferens.

. Transverse section of the testis of Colossendeis proboscidea, Sab. (sp.) ;

magnified 94 diameters.
Histological structure of the wall of the vas efferens of Colossendezs proboscidea,
Sab. (sp.) ; magnified 575 diameters.

. Transverse section of the body of Colossendeis leptorhynchus, Hoek, about

between the second and third leg; magnified 20 diameters. h, heart; v’~’,
intestine ; 0, ovary ; 7, nervous system.

. Ovarian egg of Nymphon brevicaudatum, Miers ; magnified 94 diameters.
. Section of the ovary in the fourth joint of the lee of Nymphon robustum,

Bell; magnified 94 diameters. 7, wall of the intestinal ccecum ; c, cavity
completely filled with eggs, when the animal is mature.

Ege of Nymphon longicoxa, Hoek ; magnified 94 diameters.

Section through the fourth joint of the leg of Phoxichilidium patagonicum,
Hoek ; magnified 41 diameters.

EN Dee

Abdomen, 16.
Acarus, 2.
Accessory claws, 16.
Achelia, 3, 9, 23, 24, 26, 27, 61.
echinata, 26.
hispida, 27.
levis, 27.
scabra, 147.
spinosa, 24, 26.
Alecinous, 5, 9, 26.
vulgaris, 26.
megacephalus, 26.
Affinities of the Pycnogonids with the other Arthro-
poda, 108.
Alimentary canal and its appendages, 124.
Ammothea, 9, 23, 24.
achelioides, 24.
brevipes, 24.
carolinensis, 23.
longipes, 23.
pycnogonoides, 4, 23.
Anatomy of the Pyenogonida, 100.
Anomorhynchus smithii, 99.
Anoplodactylus, 5, 82.
lentus, 33.
Andtliata, 2.
Apertures of the heart, number of the, 127.
Appendages, development of the, 138.
food-yolk in the, 138.
Arachnida, 2,
Aranea, 2.
Ascorhynchus, 4, 9, 10, 23, 25, 53, 147.
abyssi, 4, 25, 55.
glaber, 8, 25, 37, 53, 55.
minutus, 7, 25, 55, 58.
orthorhynchus, 7, 25, 57.
ramipes, 25, 56, 58.

Bdella, 2.
Blastoderm, 137, 138.
Bell, Th., referred to, 3.
Blood-corpuscles, 128.
Blood-corpuscles in the integumentary cavities, 103.
Body of Pyenogonid, description of, 14.
(ZOOL, CHALL. EXP,—PART x.—1881.)

Bohm, R., referred to, 4, 6, 49, 51, 82, 134.
Bohmia, 9, 24.
chelata, 24.
“Borstenapparat ” of the integument, 102.
Bottom, nature of the, 12.
Brachiopoda, 8.
Briinnich, 2.
Buchholz, R., referred to, 3.

Cavanna, G., referred to, 5, 122, 128, 134.
Cavities in the integument, 101.
Cephalothoracic segment, 14.
Circulatory apparatus, 127,
Claparéde, A. R. E., referred to, 4.
Claws, at the ends of the legs, 16.
Cleavage of the egg, 136.
Commensals of the legs of Pyenogonids, 144.
Cceca of the intestine, number and structure of, 8,
126.
CoLossENDEID®, 23.
Colossendeis, 3, 6, 9, 10, 23, 28, 59, 61, 70, 98.
angusta, 4, 28, 65.
borealis, 28, 98.
brevipes, 8, 28, 29, 70, 72, 73.
colossea, 147.
gigas, 8, 28, 37, 61, 64, 65, 66, 67,
147.
gigas-leptorhynchus, 28, 65.
gracilis, 8, 28, 29, 37, 59,
73, 74.
kroiyerti, 28.
leptorhynchus, 7, 28, 37, 64, 66, 67,
74, 147.
macerrima, 147,
media, 8, 28, 29, 70, 71, 73.
megalonyx, T, 11, 28, 67.
minuta, 8, 11, 29, 73.
proboscidea, 7, 11, 28, 69, 98.
robusta, 7, 28, 66.
Commissures uniting the thoracic ganglia, 116.
Commissures, circum-cesophageal, 109,
Copulation observed, 131.
Corniger hilgendorfi, 27.
Costa, O. G., referred to, 5.

CO TL ies

K 22

164 THE VOYAGE OF H.M.S. CHALLENGER.

Crustaceans, 2.

Crustacés aranéiformes, 2, 17.
Crustacea haustellata, 17.
Cyamus ceti, 2.

Davidson, referred to, 8.

Decalopoda, 6.

Depth, 8.

Disecoarachne, 9, 29, 74.

brevipes, 7, 29, 74.

Distribution, geographical, 11.

Distribution, geographical, compared with bathymet-
rical range, 10,

Dohrn, A., referred to, 5, 100, 108, 128, 129, 134,
136, 141.

Egg, 136.
Egg-packets, number, 136.
Egg packets, egg in the packet, 136,
Eggs of parasitic animals in the interior of Nymphon,
143.
Eggs in capsules in connection with the integument
of Colossendeis, 143,
Eggs, way in which they are laid, 131.
Eggs, ovarian, structure and formation, 132.
Fights, referred to, 6.
Embryos, 139.
Embryology of the Pyenogonida, 100, 134.
Endeis, 5, 9, 29, 76.
didactyla, 29.
gracilis, 29.
Eye, original, 111.
Eye, highly developed, 112.
Eye, rudimentary, 112.
Hyes, 119.
Eyes, their occurrence according to the depths they
inhabit, 120,
Eyes, minute structure of, 122.

Fabricius, J. C., referred to, 2.

Fabricius, O., referred to, 2.

Fat-cells, 127

Foxichilus pigmeus, 35.

Frey, H., and Leuckart, R., referred to, 4.

Ganglia, histological structure, 119.

Ganglia, minute structure, 118.

Ganglia, development of, 139,

Ganglia, thoracic, 112, 116.

Ganglia, paired proboscideal, 113.

Ganglia of the inner surface of the integument, 116.
Ganglia, abdominal, 117.

Ganglion, azygous proboscideal, 110.

Ganglion, supra-cesophageal, 109.

Ganglion in the course of the optic nerve, 111

Ganglion, first thoracic, 112.

Ganglionic nerve bundles of the proboscis, 113.

Ganglionic nerve bundles of the proboscis, function,
115.

Gay, referred to, 6.

Genera, list of the, 9.

Genital organs, 128.

Genital pores, 129.

Germ-layers, 138.

Glands, female, 131.

Glands, male, 128.

Glands of the ovigerous legs, 105.

Glands of the palpi, 105.

Glands of the integument, 101.

Glands of the fourth joint of the leg of the male,
106.

Glands in the first joint of the foot-jaw of the larve,
140.

Glands (pancreatic), 125.

Gnamptorhynchus, 6, 147.

ramipes, 25, 56.

Goodsir, Harry D. S., referred to, 3, 134,

Graber, V., referred to, 123.

Grenacher, H., referred to, 121.

Grube, E., referred to, 4, 5.

Hairs on the surface of the body, 104.
Hannonia, 9, 34, 92.

typica, 7, 34, 92.
Heart, 127.
Heart, development of the, 138.
Heller, C.; referred to, 4, 94.
Hesse, referred to, 4.
Hodge, G., referred to, 3.
Hoek, P. P. C., referred to, 4, 93, 100, 108, 134.
Huxley, referred to, 14, 102.
Hydrachna, 1, 2.

Insecta uptera, 1.

Integument, 100.

Integumentary glands, 101.

Integumentary cavities, 102.

Integumentary cavities, their number, 103, 104.
Intestine, structure of the wall of, 126.

Jarzynsky, Th., referred to, 3, 6.
Johnston, G., referred to, 1, 2, 134.
Joints of the legs, names, 16.

REPORT ON THE PYCNOGONIDA.

“ Knight-Errant ” species, description of, 94,
Kroyer, H., referred to, 3, 94, 134.

Lamarck, J. B., 2.

Larve, 139.

Lecythorhynchus, 6, 9, 27.
armatus, 27.
hilgendorfi, 27.

Legs, 16.

Linneus, C., referred to, 1.

Males, carrying the ova, 134.

Males, ovigerous function, exception to the rule, 135,
Male organs, 128.

Male genital pores, 129.

Male genital pores, their number, 129.

Mandibles, 14, 15.

Metamorphosis, 140.

Miers, E. J., referred to, 4, 6, 51, 99.
Milne-Edwards, H., referred to, 2, 77.

Moseley, referred to, 10.

Nerves arising from the hindmost thoracic ganglion, 7,
Nerves arising from the commissures between the
thoracic ganglia, 77.
Nerve, azygous proboscideal, 110.
Nerve, mandibular = antennary, 110.
Nerve, optic, 110, 111.
Nerve, integumentary, 112.
Nerve, for the ovigerous leg, 112.
Nerve, palpar, 121.
Nerves, paired proboscideal, 112, 113.
Nerves for the inner surface of the integument, 116.
Nerves arising from the thoracic ganglia, 117,
Nerve-rings in the proboscis, 114.
Nervous system, 108.
Nymphon, 2, 9, 10, 17, 36.
abyssorum, 22, 97.
antareticum, 19.
armatum, 44,
brachyrhynchus, 7, 19, 47.
brevicaudatum, 7, 18, 49.
brevicollum, 7, 19, 45, 147.
brevirostris, 21,
brevitarse, 21, 22.
compactum, 8, 23, 39, 41.
Jemoratum, Leach, 22.
femoratum, Rathke, 31.
fuscum, 7, 20, 48.
glaciale, 22.
giganteum, 19.
gracile, 11, 20, 65.

Nymphon gracilipes, Miers, 18, 19, 20, 43, 49.

gracilipes, Heller, 94,
grossipes, 3, 7, 20, 21, 44, 95.
hamatum, 8, 23, 36, 38, 54.
helleri, 18.
hians, 22, 97.
hirsutum, 3, 18, 21.
hirtipes, 3, 17, 18.
hirtum, 17, 18.
hirtum, vax. obtusidigitum, 17.
hispidum, 49, 51.
horridum, 18, 49.
johnstonianum, 34.
Johnstonti, 22.
longiceps, 22.
longicollum, 8, 20, 40.
longicoxa, 8, 23, 38, 42, 47.
longitarse, 20, 41.
macronyx, 4, 7, 19, 38, 95.
macrum, 147.
megalops, 4, 20. ;
meridionale, 8,11, 19, 43, 53.
minutum, 22.
miatum, 20, 21.
pallenoides, 4, 18.
pellucidum, 22.
perlucidum, 8, 12, 20, 52.
phasma, 34.
phasmatodes, 23.
procerum, 8, 23, 39.
robustum, 3, 7, 22, 97.
serrutum, 4, 21.
sluiterti, 21.
spinosum, 22.
strémit, 7, 18, 19, 42, 48, 94, 97.
styligerum, 27.

NympnHonipa, 17.

Oculiferous tubercle, 15.
(Esophagus, 125.
(Esophageal ring, secondary, 114.
Oiceobathes, 4, 9, 25.
arachne, 25.
Oomerus, 4, 9, 34.
stigmatophorus, 34.
Oorhynchus, 9, 10, 27, 59.
aucklandie, 8, 27, 59.
Openings, female genital, their shape, 132.
Organs of sense, 119.
Orithyia, 2.
coccinea, 32.

Ovaries, 131.

165

166 THE VOYAGE OF H.M.S. CHALLENGER.

Ovaries, number of, 131.

Oviduct, 132.

Ovigerous legs, 14, 15.

Ovigerous legs, functions of the, 15.

Pallene, 2, 9, 29, 30, 76, 82, 93.
attenuata, 32.
australiensis, 7, 30, 76, 79.
brevirostris, 30, 65.
chelifera, 30.
chiragra, 30, 77.
ctrcularis, 31.
discoidea 31, 169.

Phowichilidium chiliferum, 4.
digitatum, 33, 86.

femoratum, 31, 32, 84.
Jluminense, 7, 32, 81, 88.

globosum, 32.
insigne, 7, 32, 82.
johnstonianum, 34.
lentum, 33.
maxillare, 32, 33.
minor, 32.

mollissimum, 8, 11, 33, 87, 89.

mutilatum, 32.

empusa, 30.
Jluminensis, 32, 81.

oscitans, 8, 11, 33, 88, 89.
patagonicum, 7, 11, 33, 84, 86.
patagonicum, vax. elegans, 7,11, 33,86.

grubi, 30.
hispida, 31.
intermedia, 31.
levis, 78.
languida, 7, 30, 79.
lappa, 31, 82.
longiceps, 30, 81.
malleolata, 4, 31.
pygmed, 33.
spinipes, 30.
PALLENIDZ, 29.
Pallenopsis, 147.
Sorficifer, 147.
longirostris, 147.
Palpi, 14, 15.
Palpistes, 2.
Pantopoda, 17.
Parazetes, 6, 9, 26.
auchenicus, 26.
Paribeea,,5, 9, 26.
spinipalpis, 5, 26.
Pasithoe, 3, 5, 6, 9, 29.
vesiculosa, 29.
Pediculus, 2.
Pephredo, 3, 9, 25.
hirsuta, 25.
Phalangium, 1.
grossipes, 20.
litorale, 35.
spinosum, 35.

petiolatum, 32.
phasma, 34.

pilosum, 8, 11, 33, 37, 88, 90.

pygmeum, 33.
virescens, 33, 84.
Phowichilus, 2, 9, 29, 34, 35, 93.

inermis, 35.
levis, 4, 35.
meridionalis, 35.
pigmeus, 35,
proboscideus, 3, 28, 98.
spinosus, 35.

Pigment in the subeuticular epithelium of Pallene

australiensis, 101,

Plates, explanation of, 149.
Platychelus, 5, 9, 25.

sardonicus, 25.
Podosomata, 17.
Proboscis, 14, 113,
Proboscis, development of, 139.
Pseudopallene, 5, 31,

hispida, 31.

Pyenogonids of the Arctic Ocean coasts, 3.
Pyenogonids of the Cape of Good Hope, 6.

Pyenogonids of the coast of Chili, 6.
Pyenogonids of the China Sea, 5,
Pyenogonids of the Dutch coast, 4.
Pyenogonids of the English coast, 3.
Pyenogonids of Enosima, 6.

Pyenogonids of Franz-Josef Land, 99.
Pyenogonids of the French coast, 4.
Pyenogonids of the German coast, 4.
horridus, 24. Pyenogonids of the Greenland coast, 3.
inermis, 24, Pycnogonids of the Gulf of Naples, 5.
Philippi, A., referred to, 4, 76. | Pyenogonids of higher northern latitudes, 3.
Phowichilide, 34. Pycnogonids of the Japan coast, 6.
Phoxichilidium, 2, 9, 10, 29, 30, 31, 81, 92, 93, 147. Pyenogonids of Kerguelen Island, 6.

Phanodemus, 5, 9, 24.
collaris, 24.

REPORT ON THE PYCNOGONIDA. 167

Pycnogonids of the “ Knight Errant,” 94.
Pyenogonids of last English Arctic expedition, 4.
Pyenogonids of the Mediterranean, 4.
Pyenogonids of Mozambique, 6.
Pycnogonids of New England, 5,
Pyenogonids of New England and adjacent waters,
147.
Pycnogonids of North America, 5.
Pycnogonids of the North Georgian Islands coast, 3.
Pycnogonids of Northern Europe, 3, 6.
Pycnogonids of the Northern part of the North
Atlantic, 4.
Pycnogonids of the Norwegian coast, 3, 4.
Pyenogonids of Port Blair, Andaman Islands, 6.
Pyenogonids of Russian Lapland, 3.
Pyenogonids of the second German North Polar
Expedition, 3.
Pycnogonids of Singapore, 6.
Pycnogonids of the South Sea, 5.
Pycnogonids of the Straits of Magellan, 6,
Pycnogonids of the White Sea, 3.
Pycnogonids of the “ Willem Barents,” 94.
Pycnogonum, 2, 9, 35, 93.
australe, 36.
chelatum, 24.
grossipes, 44.
litoraie, 7, 35, 99.
litorale, var. tenue, 36.
spinipes, 30.

Quatrefages, A. de, referred to, 4.

Range, bathymetrical, compared with geographical
distribution, 10.
Range in depth, 7.
Range, world-wide, of the deep-sea forms, 10.
Rhopalorhynchus, 6, 28.
kroyerti, 28.
Rhynchothorax, 5, 9, 24.
mediterraneus, 24.

Sars, G. O., referred to, 4, 95, 97, 144.

(ZOOL. CHALL. EXP,—PART x,—1881.)

Savigny, J. C., referred to, 2.
Savigny, referred to, 14.
Sabine, E., referred to, 3.
Scceorhynchus, 147.

armatus, 147.
Scalpellum, sp., 2 commensal of Nymphon robustum,

98, 144.

Sch6bl, referred to, 130.
Semper, C., referred to, 13, 108, 134.
Sete on the integument, 102.
Sexual characteristics, external, 130.
Slater, H. H., referred to, 6.
Smith, referred to, 5.
Somatic cavity, 127.
Species, catalogue of the, 17.
Species, description of the Challenger, 36.
Spines on the surface of the body, 104.
Spines, denticulated ones, 104.
Spines, serrated ones, 104.
Stimpson, W., referred to, 5.
Summary of the Report, 145.

Tanystylum, 6, 9, 27.
orbiculare, 27.
styligerum, 27.
Testis, 128.
Testis, microscopical structure of, 130.
Threads, given off by the glands in the foot-jaw of
the larvee, 141.

Verrill, referred to, 5.

White, A., referred to, 5.

Wilson, E. B., referred to, 5, 82, 94, 146.
Wood-Mason, J., referred to, 5, 62.
Wyville Thomson, C., referred to, 95.

Zenker, referred to, 100, 108.
Zetes, 3, 9, 25, 88.

hispidus, 25.

spinosa, 26.

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