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THE DEPARTMENT OF CONSERVATION
STATE OF INDIANA
W. A. GUTHRIE, CHarrMan
STANLEY COULTER
JOHN W. HOLTZMAN
RICHARD M. HOLMAN, Secretary
PusiicaTion No. 7
Volume II
RICHARD LIEBER
DIRECTOR THE DEPARTMENT OF CONSERVATION
NDIANAPOLIS:
Wm. B- BURFORD, PRINTER
1920
~
/
i
| LAKE MAXINKUCKEE
\
x (\ 2s
A PHYSICAL AND
BIOLOGICAL SURVEY
BY
BARTON WARREN EVERMANN, A. M., Pu. D.
Director of the Museum of the Galitouaia Academy of Sciences
AND
HOWARD WALTON CLARK, A.B., A. M.
Scientific Assistant U. S. Bureau of Fisheries
Biological Station, Fairport, Iowa
VOLUME II
PUBLISHED BY
THE DEPARTMENT OF CONSERVATION
STATE OF INDIANA
1920
Contents
BIOLOGY— Page
TTYETH JSS SUTCTUST Ak oie SHOR Sieh eee ee ren nee erie EN RDEV, to Bree ora G
@rvlengimlenne ete peat ie etre et A, Sys geval aval leer hte aehaceh eae 7
Onc ereah MEIN eG! Cal eetcce ae ee Aesth inos F cucragelemee eu lnls, Seka Pee 8
Ona kave.(Orekoraen eet ees Ss, ected pace eee wey aT DIS, Ue cova tin hoe Mae 10
WO rclera OTE MOpberaey Hiv eter or lca tet acer sear Mem re Sere h m cates Rae cae OP RENE 27
Ordersulcnniotonaeemte ac ceettees eiarar 2 ese wha ire eather aig a ete ee 29
OnderMuniGhonpend eWnes eeraa hee oe ue ea en eae Se OM 31
OrdemColeuptena. pe eon et eae ee eet oo ta See roar 33
OxrderaDimterareenns been ks creer cio eee a: siete: back aioe teers uae 35
Ordermeenidopteracsse wel at onan es tee ae Ae acai ee eee ts et 37
Ondensldivmenopteca sts) ao. Series hie aes ee bo en ad tata a de ye 39
RT St oy INA (OUTS ee Ses cr Srvc pele toe See oles ek rene rm, Mitre Rn yy Ernie ns: 41
VU avas UTE OT RIGS EF ern ea eS eee era er RS RE a re ART ie Range ee Al
lakes and jpondsas the) home of mussels;-2..-..2.2.+2-5..5-2+--.-- 41
Origin and character of the Maxinkuckee mussels.................. AQ
Distributonkofamusselstimntne ales 2 aa: aeneite ee emcee ae 44
WIStKO TE SWE CLES teacty race hen er crer eh ora cactentin wate ac ecany epee My eaen, cot Oe dl
Molise @iloare ineia Wini@iniGks: 2, 64nnccaesn ee eucsSWsvesacseaseunsdooe 72
Distros ( Chen ORS HUN GT DZS Isic yon ales Ga A Ns PAM GIN ie ere SA ee UR ee a Lois eg ene et canes
perc OpeEMOGAPARASIUEB Ee wean ste as reas ieee aidie’ «cnr one Mo cent eral!)
WIRINeE Cera WISE S ter aee a ie rk erate de CP Se sets Long on mE Gate tat Seay start 83
APrsiiay LD OOVE TS UDI cco ki Seka e Oe S AAG RAG ore eee te Saas RP eee eae Pe ge Re od te eer 87
ne BROLOZOANS PANT © GunEINIREEVA TE Sri. cities li ea acuta. an ecco ene ae Pee
“TDIEWEE WG IEAM & oes oc es cocky is aU Ok Ae Cae SAN aa nen rie ee ar Ae RAR aaa Pe eerie Scr hon ede er 100
Thee Siomero Sie. bac tho More AER Ser es oe ER SINR cae erent a eee 100
BIG ETE Mo AUN KCL OIN ESS eee eee CMe Ry yi e noone cs Sah. he Aca Mnee Anca eye vat eet 105
he planitonwscummorwasserpluetherrecmacek. a eee cena eae ae 110
‘Reda JUTE? Ae Ae ais 0 Seth olan thy OIE eter eee es one a ie tne” hairs eee EE ee nae 17
LTTE OCLC CLOT EET RTE ees esi ro Ta ome cites aN isc Pes ee leractiaen) eeatoee al?
OTMER ESRC G) GiIACET Crue ale Fe NUROR Ae Are ace AE OO Aare ot eee Sat AUST CMGIO yk tea 119
DE(ariraeLaNG NENT ICO} Ol gy Set wee cto Gecltd areca Ove ESR ic RIC Cot Ree CREE RT ee re i mm 119
Weesrolaihe aqua hieclonan cic not ake ete ice. tuk ae ePeast > Soka es ee coos oh 119
PIG ETE HM EANNT ID gETEO RAV ieee yey tenet aye, foes Carwin is tees out chs cole tet ehte nuit sues 124
HINGT:@ CLULC GIG ee eee a eR Acs sieht eae aee een Seren teen AS Bees Canc eta: 124
CGeneralehlonalehiecl OnsMynns sc Macnee ans ane tit cre sere sche e sachanee: 128
COMPARISONS ORPAQUATIOUAND AND BRORAS=. 2.40 ..05e0 02 550 e002] oct name 133
TE TED JANIE CVEDY at tS 08 Se OWES ee ee SSE Re GRE CR me rR OM 138
Introductions see aee EAD CLR ETE Pee PO Ce Rent eae eae: 138
JATNTOM ATID) I LISI Oral SHANE 5 an oe oo ee Od hon eR ODER nen on ee coe auaccn one 141
sR eRG re cil ras wet Cae ped Ae teed cen oe gcd tunis eh ermea ehseain Se ante 141
Mbiven@ nama esse a eee a yaa eT ao UA cereale Spade aay acne ee 157
Ma eSD Ta On sare LCM ee ea OME eS a) nate a Nes A Ue me nme eer age 161
inesNouaticHelant sro takeMaximikwekeennaecdeer esl ain 165
iherAouaticenelants: ok Wostmbakets ocs.cya sm wn aeroe 4 sete eae ocin aera 192
The Ferns, Fern-Allies, and Seed-bearing Plants....................... 197
{5)
THE INSECTS
INTRODUCTION
‘Unfortunately, no entomologist was assigned to the party study-
ing the lake. No special study was, therefore, made of the insects.
This is regretted, because so many species of insects or their larve
bear an important relation to the life of the lake. The number
of species that enter directly into the menu of the fishes of the
lake is undoubtedly many and the total quantity consumed must
be very great.
Such study of the insects as we were able to make was there-
fore purely incidental and necessarily very disconnected and in-
complete. From time to time examples in various groups were
collected. These were sent to the Bureau of Entomology of the
United States Department of Agriculture, to the specialists of
which we are indebted for their identification. For assistance in
identifying the species in the various orders we are indebted to
several specialists. Professor W. S. Blatchley has helped us with
the Orthoptera, Dr. O. A. Johannsen with the Diptera, and Mr.
EK. P. Van Duzee with the Hemiptera and other groups.
An exception to this general statement may be made in the case
of the Odonata, which were collected and reported upon by Dr.
Charles B. Wilson, who spent a part of two summers at the lake
and secured such species as were to be found during that time.
ORDER APTERA
THE SPRING-TAILS
Snowfleas, probably Achorutes nivicola, were exceedingly
abundant about the edges of the pools and ponds, especially about
the woodland pond near Farrar’s. They were very active,
leaping from the moist leaves about the pond into the water or
rather upon its surface. In places they would turn the snow black.
On the occasion of a heavy snowfall late in winter an old inhabi-
tant remarked: ‘“‘This snow will remain until the bugs eat it
up.” He said that this was common belief and that in parts of
Pennsylvania some of the late heavy snows disappeared, not by
melting, but by being consumed by snowfleas! A curious super-
stition. ;
The snowfleas as they grow, often shed their skins on the sur-
face of the water, the skin remaining as a thin, white pellicle.
On March 17, 1901, they were abundant on the snow, and on
- November 1, 1904, many were seen at the edge of the lake.
(7)
8 Lake Maxinkuckee, Physical and Biological Survey
ORDER EPHEMERIDA
THE MAY-FLIES
The May-flies are probably the most important insects in rela-
tion to the fishes of the lake. Their eggs are laid in the water,
the larvee are aquatic, and both are fed upon by fishes. The May-
flies themselves, at the close of their brief lives, fall upon the sur-
face of the lake by the millions and furnish a vast amount of food
to many species of fishes,
Early in April the May-fly larvee begin to be conspicuous about
the margins of the lake and in the ponds and quiet streams. They
were first noted in numbers on April 4 (1901), and throughout
the winter they were found more or less frequently in the bottom
dredgings. About the fourth of April, they began to crowd up
near the shore in great numbers with a peculiar wriggling motion.
On April 5 they were found in immense numbers in a ditch and
some small ponds near the Assembly grounds. On April 6, millions
were seen in this ditch and they were very plentiful in many other
places. They continued very abundant until about the fifteenth
when they began to decrease in numbers, but the larvee were noted
on the 19th, 20th, and 22nd. The first May-fly imago was noted
on May 2. The next day many were seen in the woods indulging
in an aerial dance. On the fourth, many were seen in the town
of Culver, dancing in the air. From that date they kept increas-
ing in numbers, while at the same time their larve casts were more
and more abundant in the water along the shore. By May 17, the
woods were filled with insects on the wing, many of them May-flies,
and the larvee were abundant in windrows at the water’s edge.
From May 18 to 21, they were noted by the millions. On May 19
and 20 great numbers of casts and dead adults were observed in
the water and along the shore, and dead or dying adults were
very abundant in the grass and weeds around the lake. On-May
22, they began copulating and laying their eggs in the water, at the
same time being caught in great numbers by the various kinds of
fishes. The straw-colored minnows snapped them up greedily.
We caught a number of the May-flies and threw them on the water
where they were promptly seized by the fishes. They continued in
considerable numbers until May 25, when a good many were seen,
but none flying, and all rather numb. Not many were seen on
the 26th. A few were noted in the afternoon of the 27th and 28th,
and on the 29th a few stragglers were seen. On the 28th one was
observed emerging and several noted that had just emerged. In
Lake Maxinkuckee, Physical and Biological Survey 9
the evening a great many were seen flying about and on the grass.
They leave their cast-off skins on the grass a few steps back from
the lake shore. None could be seen on June 4, but on June 22 one
was seen, the last of the season.
All the above applies to a long, blackish, rather robust species
with three long caudal setze.
On June 7, were seen a few of a second species, more slender
than the other and with only two caudal sete.
It is a common belief about the lake that many fishes die as a
result of gorging themselves with May-flies, but this opinion was
not sustained by the examination which was made of the stomachs
of a considerable number of fishes found dead during May-fly
time.
In addition to the larger May-flies of early summer, a diminu-
tive form of a light brown color, but semitransparent, was present
in immense numbers in autumn, emerging one night, and laying
their eggs on the surface of the water during the next day and
evening. These were present in such numbers that they formed
regular drifts about the base of a large bullseye lamp set on the
pier, the insects flying toward the pier light and becoming tangled
up together by their long and delicate caudal stylets. Although
probably as abundant numerically as the large May-flies of spring,
these minute forms did not attract the attention that the former
did, because of their pigmy size and inconspicuous coloration. The
lisping of the minnows and other little fishes such as skipjacks,
along shore on fine autumnal evenings, was caused by their snap-
ping at these little insects as they deposited their eggs on the water
surface.
A remarkable feature about the May-flies is their habit of
moulting after the wings have formed, and after they have flown a
little distance from the Jake. It is astonishing how such a thin
transparent membran~ as their wings can be shed. The dark,
heavy species alights on the grass to make this last change but a
light transparent species of late summer is often not able to shed
the skin from its caudal stylets, but bears the entire cast-off clothes
on these, and is thus greatly impeded in its flight.
The larve of some of the large dark May-flies feed on the
softer portions of old, dead leaves, in the bottom of the water, and
some of them will, in a very short time, completely skeletonize a
leaf, leaving only the delicate lace-work of the veins.
10 Lake Maxinkuckee, Physical and Biological Survey
ORDER ODONATA
THE DRAGON-FLIES
By Charles B. Wilson
INTRODUCTION
Like the May-flies, the Dragon-flies are all aquatic and consti-
tute the most important group of insects to be found about the
lake. They are also the most attractive and graceful, in spite of
the obnoxious name of ‘“snake-feeders,’”’ which has been bestowed
upon them in the common local vernacular. They have not, of
course, the remotest connection with snakes, nor are they poisonous
or harmful in any way, as is popularly supposed. They are strictly
carnivorous and often cannibalistic in all stages of development,
the larger imagos and nymphs habitually eating the smaller ones.
But they feed chiefly upon other animals such as flies, insect
larvee, small crustaceans, worms, leeches, fish-fry and tadpoles.
They seem to relish especially house-flies and culicids, and thus
become of great economic importance through the destruction of
these pests. That the curse of house-flies and mosquitoes is kept so
delightfully within bounds at Lake Maxinkuckee is very largely
due to the untiring ministrations of the dragon-flies.
Their eggs are either laid in the water or inserted into the
tissues of some water plant or floating fragment.
As soon as the egg is hatched the nymph begins devouring other
animals. Of course, it has to be content at first with very small
ones, but as it increases in size and strength it becomes able to kill
larger and larger ones until finally it includes small fish and tad-
poles among its prey.
The full-grown nymph of one of the larger dragon-flies is fully
two inches in length with a stout muscular body and strong legs.
As soon as it is fully matured the nyi-pvh crawls up out of the
water on a rush stem, the leaf of a water :lant, a stake, a board,
or other convenient support, usually during the night or very early
in the morning. As soon as it becomes dry the skin splits along
the back, and the fully developed dragon-fly emerges. These old
nymph skins may be found about the lake during the entire sum-
mer, and often in the early morning the newly emerged imago may
be seen perched on the skin or close by. Thirty skins were taken
one morning from the inside of a boathouse on the west side of the
lake.
That the dragon-flies enumerated in the following list play a
very important part in the economy of the fish life of the lake may
be seen from several considerations.
Lake Maxinkuckee, Physical and Biological Survey 11
1. They destroy multitudes of insect adults and larve that
would otherwise serve as fish food; they are voracious feeders and
they keep at it all their lives. .
2. The nymphs of the larger dragon-flies are strong and agile
enough to catch and eat the helpless fry of many of the larger
fishes. They greatly prefer insect larve but will kill the fish
rather than go hungry.
3. On the other hand, many of the insects destroyed are ob-
noxious to man. This is especially true of the mosquitoes, gnats,
ete., which form the dragon-flies’ favorite food.
4, The dragon-flies themselves, both adults and larve, are
eaten by the fish. The young nymphs when first hatched are
nearly as good fish-food as insect larve, and are easily overpowered
by the small fish which frequent the shallow water where they live.
As the nymphs grow larger they become too wary and too power-
ful for these small fishes. At the same time they keep coming
closer and closer to the shore so that the larger fish do not get a
chance to capture them. This explains why so few nymphs were
found in the fishes’ food during July and August. During the
winter and in the early spring, when other food is scarce, these
dragon-fly larve must share with the minnows in supplying food
for the larger fish.
That the adult dragon-flies are eaten by the larger fish is a
matter of both direct observation and inference. Repeatedly in
the effort to capture some of the more wary dragon-flies a speci-
men would be knocked kelpless into the water by a blow from the
net. Often on these occasions before it could be picked up there
would come a swirl in the water and it would disappear down some
fish’s throat. It was difficult, of course, to identify the fish with
certainty, but Libellula pulchella and L. luctuosa were eaten this
way on several occasions by Large-mouthed Black Bass, while Celi-
themis eponina was taken by the Redeye. Several of the smaller
damsel-flies were taken by smaller fish. Reliable anglers also testify
that they have seen fish following a pair of dragon-flies, like Celi-
themis eponina, which fly about close to the surface over the deep
water, the female repeatedly dipping her abdomen beneath the
water to deposit her eggs, and that the fish often jump for the
dragon-flies. :
Again, dragon-flies are constantly getting into the water, par-
ticularly during a high wind and after they have finished deposit-
ing their eggs. A careful watch was kept for such individuals
- every day, but in only one instance during the entire summer was
a dragon-fly observed floating on the water. Even this one was
12 Lake Maxinkuckee,. Physical and Biological Survey
swallowed by a fish before it could be picked up; the inference,
of course, is that the others were similarly disposed of.
5. Dragon-fly nymphs in all probability prey on leeches
amongst their other food, and leeches are the most fatal parasites
that infest the lake, killing numbers of fish annually. Anything
that tends to reduce the number of leeches, therefore, will have
great economic value because they have very few enemies so far
as known.
This relation between dragon-fly nymphs and leeches is worthy
of careful study in the future. The author greatly regrets that the
lateness of the season prevented the acquiring of any positive data
on this point.
Specimens of every dragon-fly mentioned in the following list
were collected and personally identified by the author. The species
are arranged according to the admirable list of “The Dragon-flies
of Indiana” by E. B. Williamson, as published in the Report of the
State Geologist of Indiana for 1900.
Many additional facts have been taken from this list and the
author also wishes to acknowledge his indebtedness to Mr. William-
son for valuable criticism and advice given in private correspond-
ence, and for the last four species here reported, which were col-
lected by Mr. Williamson at Lake Maxinkuckee in May, 1900. The
author could not begin his collecting until the middle of July, and
it is practically certain that the months of May and June would
add ten or a dozen more species to the list.
LIST OF SPECIES
1. BOYERIA VINOSA (Say)
A rare species, shy and wary, and a strong flier. It was not
positively identified around any of the lakes visited, but was
thought to have been seen flying over Lost Lake on several occa-
sions. Three pairs were seen along the Tippecanoe River on Sep-
tember 4, the females depositing their eggs in the edge of the weeds
along the banks. One of these pairs was captured.
2. AESCHNA CONSTRICTA Say
A species seen only occasionally during the summer, but becom-
ing more common during the autumn, and_finally in the middle of
September congregating in considerable numbers around Hawk’s
marsh, which is situated about a quarter of a mile inland from the
west shore of the lake. This species, as noted by Williamson, pre-
fers the shelter of the bushes and rushes, and returns constantly
Lake Maxinkuckee, Physical and Biological Survey 13
to alight on the twigs and branches after roaming about in search
of food. Itis very active, a strong flier, and often mounts to a con-
siderable height in pursuit of its prey.
Although the abdomen of the male is seen to be highly colored
with blue on close examination, both sexes appear dull brown when
flying about.
3. PERITHEMIS DOMITIA (Drury)
One of the smallest species, frequenting the lily-pads and pick-
erel-weed, flying close te the water, and habitually keeping below
the larger and stronger species as noted by Needham.
The males congregate on the lily-pads some little distance from
the shore and are difficult to catch because they are very wary.
They can dodge a net with facility, and especially because they
fly so close to the water that it is very hard to manipulate the net.
The females are found closer to the shore and are not nearly so
numerous as the males. Their flight here in Indiana is anything
but “rather weak and a bit clumsy” as Needham records for New
York State. The author spent two hours one afternoon in early
September along the edge of the pickerel-weed at Twin Lakes en-
deavoring to catch some of these females which could be seen occa-
sionally flying about, and finally had to come away without secur-
ing a single specimen. The females seen were always unattended
by a male and deposited their eggs close to the shore amongst the
Chara and Spirogyra. One specimen that had been swept into the
water by the net was seized and eaten by a fish, apparently a War-
mouth Bass.
The adults of both sexes were obtained at Lake Maxinkuckee,
Lost Lake, Bass Lake and Twin Lakes. They were especially com-
mon at Lost Lake around the Outlet where several nymphs were
also obtained August 15, just ready to come forth as imagos.
4, CELITHEMIS EPONINA (Drury)
One of the skimmers and the largest of the genus in the State,
both sexes rust-colored throughout, with large brown spots on the
wings, the male more brightly colored than the female.
This species and Libellula luctuosa were the two most common
dragon-flies at all the lakes visited. They appeared before our
arrival and were still roaming about at the middle of September.
The female of this species is nearly always held by the male when
depositing her eggs, and the two are seen flying about together
more frequently than any other species. Since the eggs are de-
posited in the clean water, often a long distance from any vegeta-
14 Lake Maxinkuckee, Physical and Biological Survey
tion, the species is more conspicuous than most others. Then, too,
both sexes, but especially the male, are inquisitive, and perch on
the very tops of the rushes to watch the intruder. If disturbed
they return again and again to the same spot. This species is also
less dependent on the weather than most others and may be seen
flying about on cloudy days, during a high wind, or even in a driz-
zling rain.
The nymphs of this species are broad and flattened, with the
lateral margins of the last two segments conspicuously serrate.
They prefer a stump, a board, or the post of a wharf for their
final transformation and the dried nymph skins may be found in
such localities and often on the inside of boathouses.
Adults of both sexes were taken at Lake Maxinkuckee, Lost
Lake, Bass Lake, Twin Lakes, Yellow River and Hawk’s marsh.
A pair of this species which had been brushed into the water
was immediately seized and swallowed by a large bass, probably
Micropterus salmoides.-
5. CELITHEMIS ELISA (Hagen)
Not as common as the preceding species and considerably
smaller. In the coloration the red is more prominent, particularly
toward the tip of the wings. The sexes do not fly about together
as does C. eponina; the female keeps well out of sight among the
rushes and dense vegetation back from the water’s edge.
The male, however, perches on the tips of the rushes and is
nearly as inquisitive and conspicuous as the preceding species.
The nymphs are similar to C. eponina but smaller, and they
prefer a rush stem for their final transformation, and the dried
nymph skins are found in such places.
Adults were obtained at Lake Maxinkuckee, Lost Lake, and
Bass Lake; the nymphs were obtained from Lost Lake.
6. CELITHEMIS FASCIATA Kirby
A rare species only seen once during the entire summer. It
can be distinguished at once from the two other species of the genus
by its color, the general tone and the spots on the wings being black
rather than reddish brown. It is about the size of elisa and re-
sembles it in its habits, the female remaining hidden among the
vegetation along shore, while the male roams about in the rushes
over the water.
About a dozen specimens were obtained at Twin Lakes on
August 31, and they were the only ones seen.
Lake Maxinkuckee, Physical and Biological Survey 15
7. LEUCORHINIA INTACTA (Hagen)
This is the species commonly known as ‘“‘whiteface,” the desig-
nation expressing the chief peculiarity, a white face sometimes
tinged with yellow but always contrasting strongly with the sur-
rounding dark color. It frequents the marshy flats around the
lake, flying close to the water among the stems of the water plants,
so that it requires some search to find one and more maneuvering to
capture it. The eggs are laid close to the shore and the only fe-
male seen ovipositing was perched on a rush stem with the poste-
rior half of its abdomen beneath the water. The nymphs are
large with an ovate abdomen, the dorsal hooks of which are as long
as the segments which bear them. Found in Lake Maxinkuckee
and Lost Lake.
8. SYMPETRUM VICINUM (Hagen)
This is an autumnal species, not appearing until late in the sum-
mer, and is one of the smallest found. It resembles the following
species closely in size and body color, and the two can be distin-
guished only by the shape and size of the hamule and abdominal
appendages of the male, and by the structure of the vulvar lamina
in the female. It flies about as much over the shore as it does
over the water, and like the following species has a habit of hover-
ing in the air, holding itself stationary by the rapid vibration of
its wings.
It was found in considerable numbers in Hawk’s marsh and
along the Tippecanoe River, and was the last species to be seen
after frost came.
9. SYMPETRUM CORRUPTUM (Hagen)
Very similar to the preceding in coloration, especially after the
original markings have disappeared and the body has become a
dark red. It is considerably larger than vicinum, is a more rapid
flier, and rather more wary; and for these reasons very difficult
to capture.
Only a few specimens obtained from Yellow River late in
August.
10. ERYTHEMIS SIMPLICICOLLIS (Say)
This species has a wide distribution and is especially common
around the swamps and marshes and along shore. Hawk’s marsh,
the southern inlet, and Green’s marsh between Lost Lake and Lake
Maxinkuckee, swarmed with these dragon-flies during the entire
summer. They usually remain in the shelter of the dense herbage,
and often squat on the ground like Gomphus.
When they alight it is nearly always near the ground or the
16 Lake Maxinkuckee, Physical and Biological Survey
water. They may often be taken pairing in such places, and pre-
fer to lay their eggs in the shallow water along shore, amongst the
yellow algee, where the water is scarcely deep enough to cover them.
They feed largely on Diptera.
Found at Lost Lake, Lake Maxinkuckee, Twin Lakes, Yellow
River, and Tippecanoe River.
11. PACHYDIPLAX LONGIPENNIS (Burmeister)
A very cosmopolitan species found over the whole United
States, Mexico, and the Bahama Islands. Both sexes are swift
fliers, and as the males, which are most in evidence, hover near the
surface of the water and in among the vegetation they are difficult
to catch. The females remain at some distance from the water
when not ovipositing, and so are less difficult to capture. When
Ovipositing both sexes fly in and out among the cow-iilies and
arrowheads where it is hard to strike with a net, and when they
do alight it is usually on the sides of the lily stems close to the
water. This species has the curious habit of drooping its wings
and elevating its abdomen when resting, so that the insect ap-
pears to be trying to stand on its head. As Williamson remarks,
this simply furnishes the large Libellulas an excellent mark to nip
at, and the author has repeatedly seen L. luctwosa and L. pulchella
snap at the tip of the elevated abdomen and drive the Pachydiplax
away, but has never seen one of the latter killed.
This species was found during the entire summer in every lo-'
cality visited.
12. LIBELLULA LUCTUOSA Burmeister
This was the most abundant of all the dragon-flies, and was
found on all the lakes visited. It seems to prefer the higher and
drier ground and was not usually found near low and Swampy places.
It is a strong flier and often pauses and holds itself stationary by
rapid vibration of its wings.
It is also inquisitive, searching into everything, and often re-
turning to the same place when missed by the net. When fishing,
the author has repeatedly seen them snap at the cork float on the
fishing line, both while it was in the air during the casting and
while it was floating on the surface of the water.
When alighting they often prefer the side of a rush stem, or
even the bare ground. The eggs are deposited in the shallow
water near the shore, the female hovering over the spot and re-
peatedly dipping her abdomen beneath the surface in almost the
same place. The black markings of the wings make this species
very conspicuous, especially in the male where they are contrasted
Lake Maxinkuckee, Physical and Biological Survey Ly
with white. A male of this species was the only dragon-fly found
during the entire summer floating in the water. On two occasions
when knocked into the water by the net, imagos were seen to be
eaten by Redeyes.
Found on the northern and western shores of Lake Maxin-
kuckee, at Lost Lake, Twin Lakes, and Bass Lake.
13. LIBELLULA INCESTA Hagen
An extremely wary species, the males frequenting the tall reeds
and rushes along shore. They are constantly on the watch and
will not allow the collecter to approach near enough to strike them
with the net. They are also easily frightened and at once retire
out of sight and remain hidden. No female was found during the
entire season, and they must have been concealed in the grass
away from the water’s edge.
This species was only rarely seen around Lake Maxinkuckee
and Lost Lake, but was fairly common along the Outlet between
the two lakes.
14. LIBELLULA CYANEA Fabricius
Like the preceding, only the males of this species were found,
and they frequented the tall reeds and rushes along the Outlet in
company with incesta. They were not quite so wary and they also
stay closer to the ground, alighting on the sides of the rushes or
-on broken stems. The bi-colored pterostigma and the tinges of
color adjacent to it, and also at the base of both pairs of wings,
can be distinguished at some distance and at once separate this
species from any with which it would be likely to become con-
fused. The females kept themselves so closely hidden that not
one was seen during the season.
Found rarely in Lake Maxinkuckee and commonly along the
Outlet in company with incesta.
15. LIBELLULA QUADRIMACULATA Linnzus
This beautiful species was the most widely distributed and,
next to L. luctuosa, the most abundant of the large dragon-flies.
It is especially a pond-loving species, but was found also along
the banks of the two rivers visited, along the banks of several of
the cross-country ditches, around pools in the country barnyards,
and even occasionally skimming the ficids at some distance from
the water. It isa strong flier and fairly wary. It also alights but
seldom and keeps excellent watch. But it is also quite curious, and
once or twice when the net was held out quietly it flew up near
enough to be caught.
2-—17618—Vol.
18 Lake Maxinkuckee, Physical and Biological Survey
A bass, presumably Micropterus salmoides, was seen to rise and
seize an imago of this species which had been knocked into the
Yellow River with a sweep of the net. Another imago was seized
and swallowed under similar conditions in Lake Maxinkuckee by a
fish which could not be distinctly seen.
To these direct observations may be added the fact that, in
spite of their abundance, not a single example was found floating
on the water during the summer. The eggs are deposited near the
shore, by repeated dips of the abdomen beneath the surface at
nearly the same spot, similar to the practice of L. luctuosa.
The sexes are occasionally seen paired, but the female is usually
alone during egg deposition.
Found at all the localities visited but especially abundant along
the west shore of Lake Maxinkuckee.
17. PLATHEMIS LYDIA (Drury)
A large and beautifu! species, as strong a flier as the preceding,
and considerably more wary. The old pruinose males are very
conspicuous, their white bodies showing at a very long distance
against the dark background. They also proved to be the most
difficult to capture of any species, and only after repeated trials
and numerous disappointments could one be gotten into the net.
This species seems to prefer the creeks and inlets rather than the
open water of the ponds. The sexes do not pair during ovipositing,
and the female has a curious habit of placing her eggs in the water
on the top of an old lily-pad whose center has become submerged.
The male is a tireless forager and flies back and forth over the
same beat until the supply is apparently exhausted.
Found in the Outlet between Lake Maxinkuckee and Lost Lake,
at the South Inlet, and along several streams emptying into the
Yellow River.
18. CALOPTERYX MACULATA (Beauvois)
This beautiful black damsel-fly does not come out in the open
but sticks to the banks of the small streams where the thick vege-
tation throws always a cool shade. They fly slowly and not very
strongly with a sort of fluttering motion.
Their black wings, unmarked save by the white pterostigma in
the female, and the bright metallic sheen on the abdomen, make
them conspicuous amid the foliage. They congregate in consider-
able numbers, and where conditions are favorable the banks of
the stream will be fairly lined with them.
Their eggs are deposited amid the weeds and loose débris near
the bank, the sexes pairing during oviposition.
Lake Maxinkuckee, Physical and Biological Survey 19
A single male was captured on the Outlet between Lake Maxin-
kuckee and Lost Lake. They were found in great numbers on
the Yellow River, Tippecanoe River and in some of the cross-coun-
try ditches to the west of Culver.
19. HETAERINA AMERICANA (Fabricius)
A species that is common around rocky ripples in the streams
and rivers where the water is shallow and the banks are grown
up with the water willow, Dianthera. It stays close to the water’s
edge on the leaves of the willow and does not fly far even when dis-
turbed. When flying, the bright red spots at the base of the wings
of the male make it conspicuous but on alighting these spots are
concealed by the folding of the wings. The eggs are deposited
on the willow leaves at the water’s edge, and the sexes are paired
during the process. A blind sweep of the net along the willows at
such times will often capture ten or a dozen pairs.
Very common along the Outlet, at Yellow and Tippecanoe
rivers, and in the cross-country ditches to the west of Culver.
20. HETAERINA TRICOLOR (Burmeister)
This species frequents the same localities as the preceding, and
is very similar to it, the chief difference being in the posterior
wings of the male, which are brown instead of red.
It is not therefore as conspicuous when flying as the preceding,
but when at rest the only appreciable difference is one of size,
tricolor being a little the larger. Its eggs, like those of the pre-
ceding species, are deposited in the weeds at the water’s edge, the
sexes pairing during oviposition.
Found at Tippecanoe and Yellow rivers, and in a cross-country
ditch close to the Tippecanoe.
21. LESTES UNGUICULATUS Hagen
This species is somewhat smaller and not so dark colored as the
two which follow. The dorsal surface of the abdomen is an iri-
descent, metallic green, turning to pruinose in mature specimens.
The white color at either end of the pterostigma furnishes a good
mark for identification.
It flies swiftly and hides in the dense vegetation around the
marshes and along the shore, coming out only to lay its eggs.
Found in considerable numbers at Hawk’s marsh late in Au-
gust and rarely along the Outlet between Lake Maxinkuckee and
Lost Lake.
20 Lake Maxinkuckee, Physical and Biological Survey
22. LESTES FORCIPATUS Rambur
Nearly as large as vigilax, the males with slender and nearly
black abdomens, the pterostigma entirely black in both sexes.
This is also a swift flier and a frequenter of the marshes and
sedges, but it does not seem to remain concealed as persistently as
unguiculatus. Williamson says it is the first of its genus to ap-
pear in spring, and it was found late in August at Hawk’s marsh,
where it was taken in connection with the preceding species. It
was not found elsewhere.
23. LESTES VIGILAX Hagen
Notably larger than the preceding species and more brightly
colored, its colors, however, harmonize so well with its environ-
ment as to effectually conceal it. It is a slender and graceful spe-
cies, preferring the rushes and weeds around the lake rather than
along the streams. Its eggs are deposited amid the rush stems
and the sedges, the sexes pairing during oviposition. The male
retains such a firm hold of the female at this time that the two may
not only be taken together but they may be killed and placed in the
preservative still fastened together.
Found in special abundance in Lost Lake around the Outlet and
at the South Inlet of Lake Maxinkuckee and rarely along the west-
ern shore of the latter lake.
24. ARGIA MOESTA PUTRIDA (Hagen)
A large and dull-colored species which frequents the open shore
where there is plenty of sunshine. They do not alight so much
as the other species on the weeds and grasses but upon boards,
sticks, stones, etc. They are not as lively as the other species and
allow a close approach and easy capture.
In every instance observed the eggs were being deposited in
the yellow, filth-laden algze close to the shore. The male also, in
these particular instances, held his body suspended above the fe-
male at an angle of about 45° by the rapid vibration of his wings.
He was not seen to be drawn under the female, but the observa-
tions were very limited.
Found only at Aubeenaubee Bay in Lake Maxinkuckee and amid
the pickerel-weed on Lost Lake.
25. ARGIA VIOLACEA (Hagen)
A common species which remains all summer and may be found
along the shores of the lake anywhere. It prefers the dense vege-
tation close to the shore, and is also found along the banks of the
Lake Maxinkuckee, Physical and Biological Survey Dale
cross-country ditches. The sexes are usually found paired and the
eggs are deposited in the tissues of decaying weeds and stems float-
ing at the surface. During oviposition the male holds his body
suspended in the air after the manner just described for putrida.
The eggs are large and dark-colored and can be easily found in
the decaying tissues. The violet color of the male shows up plainly
among the blue and red, the orange and the brown of the species
with which it associates, and is a distinguishing character.
Found in all the localities visited.
26. ARGIA SEDULA (Hagen)
This species is found with the preceding in the rank vegetation
along streams and ditches. The males of the two species can be
told at once by their color, violet in violacea and a deep blue in
sedula. The females can then be told by their association with
the males. The eggs are deposited similarly to those of violacea
in the tissues of decaying matter floating at the surface. This
species is not nearly so common as the preceding and was found in
only two localities, along the Outlet between Lake Maxinkuckee
and Lost Lake and at the South Inlet.
27. ARGIA APICALIS (Say)
This species is similar to putrida but is brighter colored and is
not found in similar localities, preferring the streams and rivers
to the open lake shore. Here it lives-amid the rank vegetation,
venturing out only after food or for the purpose of depositing its
egos. These latter, furthermore, are never deposited in the dirty
alge near the shore but in the clearer water some distance out.
About 20 specimens of this species, including both sexes, were
taken on the Tippecanoe River in September.
28. CHROMAGRION CONDITUM (Hagen)
This species was found in considerable numbers at Hawk’s
marsh in company with two species of Lestes. They seemed to
prefer this cool, shaded swamp, and were not seen in the open or
anywhere along the lake shores. They were mating and the fe-
males were depositing their eggs in the few pools near the center
of the water where any water was visible. Of necessity the eggs
were laid in the weeds and lily-pads with which the pools were
nearly choked. Several specimens of both sexes were secured.
29. NEHALENNIA IRENE Hagen
A very small but handsome species found in the damp vegeta-
tion along some stream or ditch. In addition to its small size it is
Ze Lake Maxinkuckee, Physical and Biological Survey
bright green in color, and easily overlooked in the green foliage.
The sexes are usually paired and the female deposits her eggs on
the stems of rushes lying in the water. The eggs are pale in color
and fastened on the surface rather than inserted in the substance
of the rush.
Found along the outlet below Lost Lake.
30. NEHALENNIA POSITA (Hagen)
Another tiny species, even smaller than the preceding, living
amongst the cow-lily stems and pads out in the open lake. The
male is usually bronze-black in color, ornamented with bright yel-
low and is much easier to distinguish than irene. The eggs are
laid similarly on floating vegetation.
Found among the cow-lilies in Lost Lake, and in the South
Inlet of Lake Maxinkuckee, where it is fairly common.
31. ENALLAGMA HAGENTI (Walsh)
A brightly marked blue species found in great numbers on the
rushes in shallow water along the shores of Lake Maxinkuckee
and Lost Lake. It was more abundant in July than in August, and
had nearly disappeared by the last of the latter month. The sexes
are nearly always paired and the female seems to prefer depositing
her eggs on a broken or floating rush stem. The eggs are dark in
color and are fastened cn the surface of the floating material in
ereat black patches. The males of this species like those of Argia
have the habit of holding themselves in the air by a rapid beating
of the wings whiie the female is ovipositing. As many as 50 or
60 couples may often be seen on the same rush stem, literally cov-
ering all the available space. They are quite tame, allowing the
boat to pass so close that one could touch them by extending the
arm.
32. ENALLAGMA CARUNCULATUM Morse
Another bright blue species, a little larger than the preced-
ing and not nearly as common. The two were found associated
on the rushes in Lake Maxinkuckee and cannot be distinguished
with certainty except by an examination of the abdominal ap-
pendages in the male. Their habits of pairing and oviposition are
similar, but the eggs found were not as dark in color as those of
hageni. This species probably occurs on the other lakes but did
not happen to be found on the days when those lakes were visited.
Lake Maxinkuckee, Physical and Biological Survey V4)
33. ENALLAGMA DIVAGANS Selys
A much darker species appearing almost black when flying and
found in company with the two preceding on the rushes in the
open lake. The habits of oviposition are similar but only a few
couples were found and the species appears to be rare.
34. ENALLAGMA EXSULANS (Hagen)
Another of the darker species, the black showing mostly when
flying. It is, next to hageni, the most abundant species among
the rushes, and was also found in the open herbage along the banks
of the Yellow River.
35. ENALLAGMA SIGNATUM (Hagen)
An orange and black species easily recognized by its colors.
The abdomen is noticeably slender, the black markings showing
more prominently in the male while flying, and the orange mark-
ings of the female. When at rest both sexes show the orange
markings plainly enough to distinguish them from the associated
species of the genus. Then, too, they are not common among the
rushes, but prefer the lily-pads at some distance from the shore.
Found in the outlet of Lost Lake and in the South Inlet of Lake
Maxinkuckee.
36. ISCHNURA VERTICALIS (Say)
This is one of the species in which “at the time of imagination
two distinct color types of females appear.’”’ In one of these the
black, bluish, or grayish colors predominate, while the other is
brilliantly streaked with orange. Both of these types were found
with the green and black males upon the lily-pads in the outlet of
Lost Lake early in August. Their flight was markedly weak and
there was no trouble in capturing them. They alight, however,
only on the tops of the lily-pads and so the net must be carried
down into the water in order to capture them.
37. ISCHNURA KELLICOTTI Williamson
This species also has both the black and the orange females,
the former seemingly the more abundant. It was not found any-
where around the lake with the exception of a single male taken at
the South Inlet. But it was common at Hawk’s marsh and many
specimens of both sexes and of both types of females were secured
there. The bright blue on the upper surface of the pterostigma of
the anterior wings of the male serves to distinguish this species
from the preceding. This is a species first discovered by William-
son and therefore of peculiar interest in the state.
24 Lake Maxinkuckee, Physical and Biological Survey
38. ANOMALAGRION HASTATUM (Say)
This is another genus with two types of female, the orange and
the black. It is found flying about in the shelter of the pickerel-
weed along the shores of Lost Lake and at the South Inlet of Lake
Maxinkuckee, and also at Hawk’s marsh. It sticks closely to the
weeds and does not usually venture very far from them even to
get its food. Both sexes alight on the side of a weed stem when
Ovipositing and the female then backs down into the water. The
species was fairly common at the places mentioned.
Mr. E. B. Williamson of Bluffton, Indiana, reports the following
species not found by the present writer at Lake Maxinkuckee:
39. Anax junius, May 24, 1900, two males and one female.
40. Tetragoneuria cynosura, May 21 and 25, 1900, two males.
41. Tramea lacerata, May 21. and 25, 1900, two males.
42. Enallagma calverti, May 27, 1900, two males and one
female.
A few of our field notes for May and June, 1901, may be given
here. May 1, first dragon-fly seen; 5th, several dragon-flies; 14th
small dragon-fly; 15th, many small dragon-flies (Agrionids) ten-
erals arise out of grass in damp ponds; 16th, dragon-flies of various
sorts, mostly slender, as yesterday, some robust forms; all look
pale; 18th, some large dragon-flies seen; 20th, dragon-flies come
out of the water, emerging in great numbers; 22d, some dragon-
flies came out; 23d, a good many dragon-flies seen, both large ones
and slender steel-blue ones; some of the latter copulating; 29th,
one large and one small dragon-fly seen; 30th, several dragon-flies
seen.
June 8, many slender steel-blue dragon-flies copulating on
rushes; 6th, great numbers of small dragon-flies in grass near
lake; 8th, many dragon-fties, a small slender species coming out of
cases at noon; 12th, dragon-flies, small ones quite abundant. Saw
two large teneral dragon-flies in morning and several larvee in
afternoon; 17th, multitudes of small blue-green dragon-flies near
Outlet Bay in evening; 20th, dragon-flies laying; 21st, good many
small dragon-flies; 22d, dragon-flies plentiful.
In 1904, a rather slender red-bodied dragon-fly was noted ovi-
positing, and another was seen October 18. They seemed at this
time to be the most abundant species. They were noted copulating
and flying about October 26 and 27 and so on until November first.
Two years after the completion of the above list, another visit
was made to the lake earlier in the season and a number of addi-
Lake Maxinkuckee, Physical and Biological Survey PAB)
tional species were observed. These are probably as common as
many of the original list, but they escaped notice during the first
season, or they may have appeared and disappeared previous to
the beginning of observations.
43. GOMPHUS EXILIS Selys
Common on the banks of the Outlet June 28, 1909, where it
alighted on the grass and on the lily-pads and spatter-docks over
the water. Of nine captured, eight were males, all of which were
feeding on teneral damselflies.
44. GOMPHUS LIVIDUS Selys
Captured at the Gravelpit on the west shore of the lake July 1,
in the grass along shore and back some distance from the water.
Unlike most species of this genus, it alights on trees and bushes
as well as on the ground.
45. GOMPHUS FURCIFER Hagen
A single female was captured at the Gravelpit in company
with the preceding species July 3. She was holding a teneral Tet-
ragoneuria, which was about half eaten.
46. GOMPHOIDES OBSCURA (Rambur)
Common along the sandy beaches on the western side of the
lake June 30. A pair that were mating and several single males
and females were secured. This species has the habit of perching
on the reeds out in the water after the manner of Celithemis, but
it chooses short and stiff reeds rather than tall ones that sway in
the wind. It flies only a short distance from its perch and returns
to the same spot repeatedly. In 1909 these dragonflies were still
common on July 15, but none was seen in other years.
47. ANAX JUNIUS (Drury)
Common around Lost Lake and along the Otulet on June 26,
but not any seen on Lake Maxinkuckee. Afterward, on July 14,
a single male was secured at Norris Inlet.
48. EPICORDULIA PRINCEPS (Hagen)
Common in Lake Maxinkuckee and Lost Lake June 27, where
they were patrolling the shore after the usual manner of this
species. A single one was seen at Norris Inlet July 14. These are
the only records for the species.
26 Lake Maxinkuckee, Physical and Biological Survey
49. TETRAGONEURIA CYNOSURA (Say)
Common at Lost Lake where it flies about over the water con-
tinually for long periods without alighting. Eight specimens were
secured at the Gravelpit on Lake Maxinkuckee July 38, but the
species disappeared very quickly after that date.
50. LADONA EXUSTA (Say)
A few were seen on the east bank of the Outlet along the edge
of the woods July 4, in company with Libellula incesta and L.
cyanea. Several pruinose males were captured, and the species
was afterward seen along the west shore of Lake Maxinkuckee.
51. LIBELLULA PULCHELLA Drury
Common along the west shore of Lake Maxinkuckee in 1909.
A large and powerful dragonfly which captures and eats many
moths and small butterflies as well as other insects. It is more
watchful and wary than many of the other species, but while eat-
ing, can be approached easily.
52. TRAMEA LACERATA Hagen
A single male captured as it was flying along the shore of
Lake Maxinkuckee. The black bases of the hind wings are very
conspicuous when the insect is on the wing and make it easy to
identify. Many were seen along the west shore, particularly at
the Gravelpit, and it was also noted at Norris Inlet on July 14.
53. SYMPETRUM RUBICUNDULUM (Say)
Several specimens were captured in Hawk’s marsh in 1908, and
a single male on the banks of the Outlet in 1909.
54. LESTES CONGENER Hagen
A single pair taken together in Hawk’s marsh August 24, 1908.
55. ENALLAGMA GEMINATUM Kellicott
A single pair taken together in Lost Lake August 22, 1908.
56. ENALLAGMA POLLUTUM (Hagen)
Two pairs taken together in Lost Lake on the lily-pads Au-
gust 22, 1908, and a single male on the lily-pads at Norris Inlet
August 25.
Lake Maxinkuckee, Physical and Biological Survey 21
ORDER ORTHOPTERA
GRASSHOPPERS, CRICKETS, KATYDIDS, ETC.
Even if they had nothing to do with the lake and its life, a dis-
cussion of the insects of the region, or, indeed, of the insects of
any region, without mention of the Orthoptera would be, to use
a singularly unhappy but hackneyed simile, like the play of Ham-
let with Hamlet left out; for there is no other group of insects
more prominent, perhaps one could even say so prominent, in the
consciousness of men. What the gaudy butterflies are to the eye,
the Orthoptera are to the ear. Indeed, grouping the various in-
sects according to the sensations caused by the most familiar mem-
bers we might say that we know the Hemiptera by the sense of
smell,* the Diptera by the sense of touch, the Lepidoptera by the
sense of sight, the Hymenoptera through their works and indirectly
by the sense of taste, and the Orthoptera by the sense of hearing.
This group it is that adds to the thought of insect life nearly
all of its lyrical element; and it is probably on account of this that
the one notable exception is popularly known as the ‘“‘locust’’, just
as country boys think of the chimney swift as a “swallow” because
of its general similarity in habits. As will be seen later, how-
ever, one group of these insects is of peculiar interest and bears a
special relation to the life of the lake.
Not all the Orthoptera are choral. There are the cockroaches,
which are, very fortunately, scarce or absent in the houses about
the lake. A wild, or native species was, however, abundant and
nearly ate the bindings off of some books kept in the tent, and the
lank, silent walking-sticks, Diapheromera femorata, were not rare
in woodlands. Of greatest economic importance were the grass-
hoppers.
Chis group of insects is important because certain species enter
so largely into the food supply of many species of fishes. By all
odds the most popular as well as the most killing bait used by the
anglers who frequent the lake is the grasshopper. It is a choice
bait and always attractive, not only to both species of black bass,
but also to the rock-bass, bluegill and yellow perch, and not wholly
rejected by the warmouth, crappie, calico bass, wall-eyed pike,
pumpkinseed and other sunfishes.
It has been shown elsewhere in this report that the small boys
who sell grasshoppers to the anglers at this lake derive therefrom
an annual income of at least $200.
*We feel mosquitoes, smell bugs, taste honey (and if reports of lumber camps are to be believed, some of
the men eat the large black ants for their acid taste and intoxicating effects), see butterflies, and hear
crickets, grasshoppers and katydids.
28 Lake Maxinkuckee, Physical and Biological Survey
Fortunately for the angler, grasshoppers of various species are
abundant in the fields, meadows and waste places about Lake Max-
inkuckee. The prairie meadows to the west of the lake have al-
ways been favorite localities for the hoppers, but in season they
are abundant everywhere. They become popular for bait and are
in demand just as soon in the summer as they have attained proper
size and are in sufficient numbers to be secured in large quantities.
This may happen as early as the first week in July; though usually
the anglers will not be using hoppers exclusively until toward the
latter part of that month.
In 1901, a few anglers began using hoppers as early as July 5,
and with good success. On July 7, grasshoppers were heard sing-
ing in considerable numbers. August is, however, the best month.
It was observed in 1900 and 1903, which were particularly good
fishing seasons, that nearly all the good catches made in that month
were on grasshoppers. They continue to be used just as long as
they can be found, which will ordinarily be until about the last of
September or just before the first frosts have come. In 1900 they
were in use at least as late as October 1.
Several different species are used; the principal one being
Melanoplus differentialis, a large red-legged species, abundant in
all fields, particularly among ragweeds along the edges of corn-
fields. Another species of the same genus, M. bivittatus, is equally
good, though somewhat less common. Still another is M. femur-
rubrum. Various other species are used; indeed, almost any kind
of grasshopper appeals more or less strongly to most of our fresh-
water spiny-rayed game fishes.
In September and October when it is difficult to get grasshop-
pers, black crickets (of the genus Gryllus) make good bait, par-
ticularly for bluegills.
Katydids of various species (particularly Pterophylla camelli-
folia and Neoconocephalus robustus) are common. They were
first heard singing July 23. From then on they could be heard
every favorable night.
In 1900 we became especially interested in a particularly musi-
cal, broad-winged katydid (Pterophylla camellifolia) that took up
its station in a large white oak tree near our cottage. We first
took note of it on the evening of July 23. From that date on it
was heard on every suitable quiet night until September 27 when
it missed although the night was a favorable one. The next night
it was heard again and it continued noisy nearly every night for
more than three weeks. About the 18th of October its song began to
Lake Maxinkuckee, Physical and Biological Survey 29
weaken, particularly on the coolest nights, when it would give only
a few very weak calls, usually consisting of “she did’; sometimes
of “she did, she did,” slow, deliberate, and weak. On the night
of October 24 we heard a single low, weak, slowly uttered ‘‘she
did,” after which it became quiet and we heard it no more.
Crickets, especially the common black field cricket (Gryllus as-
similis lactuosus), were fairly common and musical, especially in
the fall. Our notebooks have many records of their singing, the
earliest entry being May 17. From then on they were heard almost
nightly and often in the daytime, until November 22. Mole crickets
(Gryllotalpa) are rather common about the lake. Their burrows
may be often seen in the sandy beaches. Their interesting musical
note can often be heard, especially in August. Tree crickets were
abundant, especially in low copses and thickets and, more than
anything else except perhaps the katydids, made the autumn nights
musical.
The following species of Orthoptera have been identified as oc-
curring about Lake Maxinkuckee:
Diapheromera femorata Say
Chorthippus curtipennis Harr.
Dissosteira carolina Linn.
Melanoplus atlanis Riley
Melanoplus bivittatus Say
Melanoplus differentialis Thomas
Melanoplus femur-rubrum DeG.
Melanoplus fasciatus (Barnston-Walker)
Scudderia curvicauda DeG.
Pterophylla camellifolia Fabr.
Neoconocephalus robustus Scudd.
Gryllus assimilis lactuosus Serv.
ORDER HEMIPTERA
Bucs, CICADAS, APHIDS, AND SCALE INSECTS
Of all the groups of insects found in the lake and in the immedi-
ate vicinity, the least attention was paid to the Hemiptera or bugs.
In the course of seining, raking weeds, taking plankton, etc., vari-
ous forms would attract the attention either because of form, color,
habit or abundance, and these would be preserved for identification.
The Water Boatman, Corisa (Arctocorisa) interrupta Say, ap-
pears in our collection and was probably common in the lake. We
have no special notes concerning it.
30 Lake Maxinkuckee, Physical and Biological Survey
The Back Swimmers, Notonectide, are represented by Noto-
necta undulata Say, obtained November 25, 1904, in the outlet of
Lost Lake, and N. irvrorata Uhl., but we have no special notes.
The Water Scorpion, Ranatra fusca P. Beauvois, attracted at-
tention by its commonness, and by the fact that it was usually in
evidence while one was collecting minnows and darters out of the
seine. The queer egg cases, laid in rows in bits of floating sticks
or rushes, with the two long white setz projecting, had aroused
considerable curiosity which was not satisfied until a Ranatra was
seen ovipositing in Lake Phalen, Minnesota, in 1907.
The Giant Water-bug or ‘‘Electric-light Bug’’ was occasionally
seen. On December 7, 1906, one was observed creeping along on
the under side of the clear ice, and on October 1, 1904, one was
noted in the water near the Monninger cottage. Its smaller rela-
tive, Belostoma flumineum Say, was common in the lake and at-
tracted attention through the habit of the male of carrying the
eggs about on his back. It was obtained in various parts of the
lake, in Aubeenaubee Bay, Aubeenaubee Creek, in Culver Inlet,
and Lost Lake. On August 6, 1906, the young were observed
hatching, the larve showing red eyes. These bugs as found in
the lake are generally infested, sometimes pretty badly, with sac-
like red objects attached to them, the young of one of the water-
mites. On August 1, 1906, one was found in Lost. Lake that had
just moulted.
Peculiar toad-shaped bugs, Gelostocoris oculatus, were abundant
along the sandy shore on the east side of the lake. Some were
collected August 6, 1906.
The common water-strider Gerris (Hygrotrechus) remigis Say,
was common in the creek in Overmeyer’s woods and in various
pools in the region about the lake.
The thread-legged bugs were represented by the long legged
Emesa, Emesa longipes, which was very abundant in the Arling-
ton waiting-room on one occasion, the insects looking a great deal
like walking-sticks and presenting an odd appearance when in
flight.
Individually by far the most abundant bug noted in the region
was the Lace Bug, Corythucha ciliata Say, which was almost al-
ways present—both old and young—on the underside of the syca-
more leaves. They ate the green color cells from the leaves, leav-
ing them an unattractive sickly white in color. Under magnifica-
tion these are the most attractive and dainty of the insects, the
whole creature resembling a frosty lace.
Lake Maxzinkuckee, Physical and Biological Survey 31
Among the more common, homely bugs, the most abundant
species was Oncopeltus fasciatus Dall, on the milkweed blossoms.
Cicadas, or harvest flies, were conspicuous by their absence.
Throughout Indiana, as in other parts of the country, one of the
characteristic sounds of summer is that of the Dog-day Locust or
Harvest Fly. We have no record of hearing it at the lake. It is
possible that it does not like the sandy soil.
An odd-shaped tree hopper, Enchenopa binotata, was noted in
abundance laying white eggs in masses on twigs of the hop tree,
Pielea trifoliata, August 10, 1906, and examples were collected.
Plant lice were abundant on the pondweed leaves (Potamogeton
natans) in Lost Lake, making a messy looking mass. They were
also present, but in fewer numbers, on the water-lily leaves.
ORDER TRICHOPTERA
THE CADDIS-FLIES
The Caddis-flies are among the most interesting of our insects.
Although about 150 species have been described from America,
there are doubtless many remaining undescribed.
The adults are not well known to the general public, in spite
of the fact that at times they appear in myriads. The larve,
which are aquatic, are much better known. Every one who has
spent any time along mountain streams, or even about other
streams, or lakes, if at all observing, can not fail to have noticed
the cleverly built, often beautiful, cases which these larve build
of sand, brightly colored pebbles or bits of wood, held together by
silken threads. As Professor Kellogg has well said:
There is a great variety in the materials used and in the size and shape
of the cases, each kind of Caddis-worm having a particular and constant style
of housebuilding. Grains of sand may be fastened together to form tiny,
smooth-walled, symmetrical cornucopias, or small stones to form larger, rough-
walled, irregular cylinders. Small bits of twigs or pine-needles may be used;
and these chips may be laid longitudinally or transversely and with projecting
ends. Small snail shells or bits of leaves and grass serve for building mate-
rials. One kind of Caddis-worm makes a small, coiled case which so much
resembles a snail shell that it has actually been described as a shell by con-
chologists. * * * An English student removed a Caddis-worm from its
case, and provided it with small bits of clear mica, hoping it would build a
case of transparent walls. This it really did, and inside its glass house the
behavior of the Caddis-worm at home was observed.
Most Caddis-worm cases are free and can be carried about by
the worm as it wishes, but many of them are fastened to rocks,
stones or other objects in the bottom of the stream or lake. Whena
32 Lake Maxinkuckee, Physical and Biological Survey
Caddis-worm is ready to pupate, the pupa comes out from the
submerged case, crawls up on some support above the water and
there moults, the winged adult (imago) soon flying away. Some
kinds, however, emerge in the water.
The Caddis-flies do not feed and are short-lived. They lay
their eggs in or near the water where they hatch into Caddis-
worms, thus completing the life cycle.
We find among our field notes the following:
October 29, 1900, collected a number of leathery caddis-cases
at the Weedpatch. They were made of bits of shell fastened to-
gether. The larva sticks four legs out of the orifice and is able to
crawl about freely. February 11, 1901, Caddis larvee noted. June
10, Caddis-flies looking like small white moths, also lace flies, flut-
tering in the open woods, making a continuous hum through the
night. June 11, noticed ovipositing in the lake; water full of
larve casts, especially early in the morning; Caddis-flies very
glaucous, looking like moths at a distance; they stay among the
trees in the shady woods; collected a number and observed that
their antennz were very long. June 12, about 4 p.m., a strong
southwest wind blew great myriads of Caddis-flies toward the lake;
the swarm was thick and white and the appearance was that of a
brisk snowstorm. June 13, while passing a maple tree on Long
Point in the morning, an immense swarm of Caddis-flies came out
of it, flying with a peculiar helpless, half-falling flight. June 14
to 17, many Caddis-flies and midges observed. June 22, caddis-
flies laying in the water. October 18 to 29 (1904), Caddis cases
(Helicopsyche?) like small snail shells, very abundant, attached
to rocks and on bottom in Outlet Bay near Holbrunner’s, and
along the east side of Long Point. Also a number of empty chim-
ney-shaped cases were seen, and several flattish ones moving about
making burrows in the sandy bottom near Holbrunner’s. October
5 and 10, many fine examples of Helicopsyche on stones, etc., in
shallow water near shore. July 27, collected three of a scute-like
kind while screening sand; put them in a saucer of water but they
soon died. One species of Caddis-fly was abundant, a frail, glauc-
ous, moth-like insect, the leathery cases of which were abundant
on the stems of Potamogeton, Scirpus, ete., from midsummer until
in the spring when (about June 10) they emerge in great num-
bers, and the next day are busy ovipositing. A peculiar case look-
ing like a snail shell built of pebbles was found in numbers in the
same place.
The caddis-cases that attracted the most interest were the flat
Lake Maxinkuckee, Physical and Biological Survey 33
ones referred to above, found near shore in sandy bottom along
the east shore of Long Point. Just as one species of Caddis-worm
builds a case resembling a snail shell, the case of these bears some
resemblance to a limpet, or to a marine genus of mollusks, Crepi-
dula, showing how similar conditions of life lead to similarity of
form. The caddis-case under discussion is very, effectively con-
cealed by its resemblance to the sand on which it is found; most
were found while screening sand in the search for young mussels.
The central portion of the shell—that is the first, part built—is
composed of very minute sand grains; around the margin, either
because the larva has become stronger and can handle coarser ma-
terial, or because they build up more rapidly, coarser bits are used.
When the builder has chosen one sort of material it appears to
make some effort to match it. In some cases the valves of the
shells of a very small bivalve mollusk, Pisidium, were used around
the margins and the cases thus built were especially attractive.
The larva lived in a little arch or compartment below the roof of
the case.
ORDER COLEOPTERA
THE BEETLES
No special attention was given to the beetles except a few
species found in and about the water. No one could help noticing
the tiger beetles which were present in considerable swarms on
' sandy beaches and were conspicuous on hot days, hopping or jump-
ing before one walking along shore. There were two kinds pres-
ent, a brown one and a bright, metallic green.
Whirligig beetles, Dineutes, were common about the edges of
the lake. Some were seen swimming about as late as November 4.
The Predaceous Diving Beetles (Dytiscus) were not especially
common in the lake. We obtained, however, an example of D.
hybridus.
The water-scavenger, Hydrophilus, appéared more common in
pools and ponds than in the lake itself. The egg cases were com-
mon on the under sides of the thallus of Riccia.
Small hemispherical or rather oval red beetles with black spots
(Melasoma interrupta) were exceedingly abundant on the willows
along shore early in the spring of 1901. The adults laid the eggs
on the leaves of the willows and the young which soon hatched
almost defoliated the trees, and the water of the lake was almost
covered with the adult beetles.
The “water penny”, the larva of Psephenus lecontei, was com-
-mon under pebbles in the lake, its chiton-like form arousing con-
3—17618—Vol. 2
34 Lake Maxinkuckee, Physical and Biological Survey
siderable interest. The most interesting of the beetles in the lake
is a little creature belonging to the genus Stenelmis that lives in
the masses of lime or marl or alge which grow on the exposed
ends of the freshwater mussels living in the lake. This growth or
deposit is most marked on the shells of Lampsilis luteola which is
the most abundant species of mussel in the lake. These mussels
burrow more or less in the mud or sand, leaving usually one-tenth
to one-fifth of the posterior end exposed to the water. Upon this
exposed portion a mass of lime and algze slowly accumulates and
finally becomes one-fourth to one-half inch thick. In this mass
the little beetle, recently described as new by Professor W. S.
Blatchley from coilections made by us and named by him Stenelmis
sulcatus, is quite common; a collection of 20 to 30 mussels would
furnish 50 to 100 examples of the species. Specimens have been
found in similar masses on rocks in the lake, and it probably
occurs on other species of mussels though we have found none on
any except Lampsilis luteola.
Click-beetles, especially the large conspicuous eyed Elater, Alaus
oculatus, were seen occasionally. The beautifully phosphorescent
larva of one was obtained at night on Long Point June 28, 1901.
The fireflies or Lampyrids were exceedingly abundant in low
grassy places, flashing everywhere at night. The phosphorescent
larvee were abundant in the grass along the Inlet.
A few stag-beetles were seen on Long Point.
Snout Beetles, especially acorn weevils, were common, and most
acorns were attacked. One was seen on an acorn, and a snout-
beetle was seen June 7, 1901, with patches of eggs, on the tip of
a bulrush.
The only species of beetles represented in our collections are
the following:
Stenelmis sulcatus Blatchley
Dytiscus hybridus Aubé.
Ilybius biguttulus Germ.
Acilius fraternus Harris
Tropisternus glaber Herbst.
Photuris pennsylvanica DeG.; larve.
Dineutes sp; larvee.
Psephenus lecontei Lee
Cicindella sp.
Melasoma interrupta
Lake Maxinkuckee, Physical and Biological Survey aS:
ORDER DIPTERA
THE FLIES
The genera of dipterous insects found about the lake that pos-
sess most interest to us are Chironomus, Culex, and Anopheles.
Of these the genus Chironomus is economically the most import-
ant. One species occurs at the lake in untold billions. Late in
September and early in October, 1913, one large yellowish, mos-
quito-like species of Chironomus appeared in immense numbers.
They were noted every evening at least from September 21 to
October 5, filling the air at Long Point from near the surface to a
height of 20 or 30 feet, and making it musical with their incessant
humming. They were particularly abundant on the evening of
October 5. They appeared in enormous numbers sometime before
dark and continued late in the night. They literally filled the air;
a person could not walk about without being annoyed by their
striking him in the face. It was evidently their nuptial flight, and
was kept up for about two weeks during warm quiet evenings.
The flight would usually begin an hour or so before dusk and con-
tinue well into the night. They were in evidence in some numbers
throughout the day, but the great flights always occurred late in
the evening. Various species of birds were observed feeding upon
these insects, among them nighthawks, yellow-billed cuckoos, red-
headed woodpeckers, yellow-rumped warblers, and song sparrows.
The cuckoos, warblers, swallows and sparrows would pick them
from the limbs of trees, while the others took them on the wing.
At the same time, vest quantities of the cast-off skins of the
larvee of these insects were washed up on shore where they could
be seen in great masses along the edge of the water. There they
were fed upon by Wilson’s snipes, sandpipers, rusty blackbirds and
even red-winged blackbirds. They were also fed upon by various
fishes such as straw-colcred minnows, grayback, top-minnows and
the like. The larve, known as red worms, are very abundant in
all parts of the lake; they have been dredged up from even the
deepest parts. They are choice food for the fishes and no doubt
constitute an important part of the daily menu of the suckers, min-
nows, darters, sunfishes and the young of the basses and other
spiny-rayed fishes. A 75-pound buffalo-fish contained almost a
bucketful of Chironomus larve.
About the middle of August, 1906, a mass of eggs of a smaller
species of Chironomus was found and placed in a saucer. The
eggs hatched in a few days into little wrigglers which soon became
worm-like and built for themselves little tubes in which they
36 Lake Maxinkuckee, Physical and Biological Survey
stayed. The tubes varied greatly in size and were probably built
up of the excreta of the wrigglers. These wrigglers would some-
times leave their tubes and swim about near the surface, and fed
greedily upon Spirogyra which was put in the dish. Chironomus
larvee were observed to be abundant throughout the lake during
the winter. They were easily obtained by dredging. They were
either naked or enclosed in gray mud cases. When naked their
bright colors made them very conspicuous. Some that were placed
in a jar with some sticklebacks proved very attractive to the latter
which snapped them up greedily. Some naked larve placed in a
tumbler of dirty water cver night encased themselves.
Another group of dipterous insects of importance is that of the
mosquitoes. Fortunately for the summer cottagers, however, mos-
quitoes rarely appear in sufficient numbers about the lake to be
much of a pest. While there are several marshy tracts near the
lake which furnish faverable breeding grounds for mosquitoes,
they are, in most instances, sufficiently remote from the cottages,
or else the winds are favorable for keeping them away. They are,
of course, more common in some seasons than in others. Our notes
speak of them as common in certain places November 2, 1902 and
1903, July 3, 1904, September 12, 1907, and September 2, 1913.
They are said to have been rather bad during the summer of 1913.
Unfortunately, very little attention was given to preserving speci-
mens of the various species of insects and our collection contains
but three species of mosquitoes, viz: Anopheles quadrimaculata,
Culex stimulans and Culex excrucians. Doubtless others occur.
Corethra larve are common in the lake, descending into the
deeper waters; they are also common in the woodland ponds.
Following is a list of the species of Diptera represented in our
collections from Lake Maxinkuckee:
Psorophora ciliata Fabr.
Anopheles quadrimaculata Say
Culex stimulans Walk.
Culex excrucians Walk.
Tanypus monilis Linn.
Calliphora erythrocephala Meig; larvee.
Chironomus meridionalis Johan.
Chironomus decorus Johan.
Chironomus cayuge Johan.
Tipulid, probably the genus Tipula.
Tenytarsus dives.
Ablabecemyia montis Linn.
Lake Maxinkuckee, Physical and Biological Survey i |
It is worthy of note that the deer-fly, Chrysops, which we found
very annoying at Twin Lakes a few miles north, is not common at
Lake Maxinkuckee. At Twin Lakes where the deer-flies were par-
ticularly pestiferous on one occasion a robber-fly came along and
caught one just about to bite.
ORDER LEPIDOPTERA
BUTTERFLIES AND MOTHS
Butterflies are abundant about the lake. The great diversity
of soil, moisture, and vegetation, furnishes conditions very favor-
able to the development of this group of insects. The number of
species is therefore large, and many of them are represented by
numerous individuals during their season.
Perhaps the most conspicuous species and one that may be seen
throughout the greatest number of months is the milkweed but-
terfly (Danaus archippus). Although not the first to appear in
the spring it nevertheless appears quite early, and it is the species
that may be seen in numbers quite late in the fall. Only a small
amount of sunshine and warmth is sufficient to entice it to wing,
and single individuals and often groups of three or more may be
seen on almost any warm day until late in October or even in No-
vember. It is usually most in evidence, however, during the middle
of summer (July and August) when the common milkweed
(Asclepias syriaca) is in flower. Then about every clump of this
showy plant, so abundant along the railroad and on the borders
of woods, old fields and ill-kept fence rows, these large butterflies
of rich brown and black may be seen in abundance. Late in the
fall, even after the first biting frosts have changed the marshes
and byways from their summer green to the somber browns and
grays of late autumn, several of these butterflies may be seen by
any one who goes afield on the still Indian summer days.
Sometimes remarkable flights of the Milkweed Butterfly occur.
Such a flight was witnessed at noon on September 24, 1907, when
several hundred were seen flying from the direction of the lake
over Arlington station and into Green’s woods. They flew against
a strong wind but were able to make good headway. Some of them
were much higher than the telegraph poles, others were lower down
and sailed upward against the wind. At times only two or three
would be in sight, then 20 to 30 would come flying close together.
The flight continued for 15 or 20 minutes.
The common Cabbage Butterfly (Pieris rapx) is, of course, an
38 Lake Maxinkuckee, Physical and Biological Survey
abundant species. Our notes record it at various dates from April
27 to September 27. The larvee are abundant and doubtless often
drop or wash into the lake.
On October 9 and 10, 1907, the caterpillars of the Cabbage But-
terfly were crawling thickly over the east side of a house on Long
Point and pupating. Many were dead. They had apparently been
stung by ichneumon flies, many of which were seen near the un-
affected ones. Beside the dead caterpillars were clusters of golden
silky cocoons, about 18 in number, probably of ichneumon-flies.
The Southern Cabbage Butterfly (Pieris protodice) is also com-
mon. It was noted thrcughout the season from June 11 to Octo-
berva ts
The earliest species to appear in the spring is the beautiful
Mourning Cloak (Aglais antiopa). As it hibernates through the
winter it may be seen quite early in the spring when the first warm
days revive and bring it forth. Our earliest record is for April
10, but it doubtless appears before then. Our latest record is on
October 30, when one was seen hidden under a hollow log. On
April 26, three were seen on flowers of Bebb’s willow.
The Red Admiral (Vanessa atalanta) is another pretty species
which appears early in the spring and remains until late in the fall.
Our early and late dates are June 7 and October 29. This species
is fairly common.
Hunter’s butterfly (Vanessa virginiensis) is another beautiful
but less common species which we have noted from May 3 to Octo-
ber 29.
The genus Polygonia is represented by at least two species
(Polygonia comma and Polygonia interrogations). These are
also among the species which appear early in the spring and re-
main later in the fall. They are solitary in their habits; not often
are more than one or two seen together. Our notes mention Poly-
gonias at various times from April 4 to November 2.
Of the swallowtail butterflies perhaps the most common is the
Black Swallowtail (Papilio troilus). Our records mention it on
various dates from May 9 to September 27. The zebra or Ajax
Swallowtail (Papilio marcellus) and the large yellow swallowtail
(Papilio glaucus f. turnus) are apparently not common.
The following is a list of the species of butterflies noted at
Lake Maxinkuckee:
Papilio polyxenes Fabr.
Papilio troilus Linn.
3. Papilio marcellus Cram.
Ne
Lake Maxinkuckee, Physical and Biological Survey 39
4. Pieris protodice Bd.-Lec.
5. Preris rapx Linn.
6. Hurymus philodice Godt.
7. Hurema euterpe Men.
8. Danaus archippus Fabr.
9. Cissa eurytus Fabr.
10. Satyrodes canthus Linn.
11. Cercyonis alope Fabr.
12. Cercyonis alope Fabr. var.
15. Cercyonis alope nephele Kirby
14. Argynnis cybele Fabr.
15. Brenthis myrina Cram.
16. Phyciodes tharos Drury
17. Polygonia interrogationis Fabr.
18. Polygonia comma Harr.
19. Aglais antiopa Linn.
20. Vanessa atalanta Linn.
21. Vanessa virginiensis Drury
22. Basilarchia archippus Cram.
23. Libythea bachmani Kirt.
24. Heodes hypophixas Boisd.
25. Heodes theo Boisd.
26. Hveres comyntas Godt.
27. Lycenopsis pseudargiolus Bd.-Lec.
28. Epargyreus tityrus Fabr.
29. Cocceius pylades Scud.
30. Pyrgus tessellata Scud.
31. Thanaos persius Scud.
32. Ancyloxypha numitor Fabr.
38. Callosamia promethea Drury (moth)
D4. Scepsis fulvicollis Hubn. (moth)
3D. Hubaphe ferruginosa Walk. (moth)
36. Utetheisa bella Linn. (moth)
37. Xanthotype crocataria Fabr. (moth)
ORDER HYMENOPTERA
THE BEES
Our notes on the Hymenoptera are very few indeed. These,
the most highly organized of insects, have the least to do with
aquatic life.
Judging from the number and kinds of oak galls on the trees
40 Lake Maxinkuckee, Physical and Biological Survey
about the lake, gall-wasps are abundant and represented by various
species.
Of the Braconids, Microgaster is common, and the parasitized
caterpillars that have fallen a prey to it have been frequently found
about the lake.
Ants are not so common as to be a nuisance. There are, how-
ever, a few large dome-shaped ant hills along the border of the wet
ground near Lost Lake and along its outlet down by Walley’s
woods.
The solitary wasps are represented by the potter-wasp, Humenes
fraterna, which builds its exquisite little clay vases on slender
twigs down at the edges of the woods toward the south end of the
lake.
Wasps and Yellowjackets are occasionally seen. Hornet’s nests
were rather rare. On November 2, 1902 a big hornet’s nest was
seen in a white oak in Walley’s woods 30 feet up. It had been shot
into. Another very large nest was found October 24, 1907 beside a
lane west of the ice-houses near the tamarack swamp. It was built
on some wild-cherry sprouts, the nest almost or quite touching the
ground. Some one had torn away a part of one side. Tearing the
nest open it was found that many of the grubs were just emerging
and crawling about. A photo was taken of the nest. Dr. L. O.
Howard says that this hatching in the fall is very unusual.
There is a current popular belief that if hornets build their
nests high in the trees it is a sign of an open winter, while if they
are built close to the ground the winter will be severe.
On October 11, 1913, a fine large nest was seen in a tulip tree
in Overmeyer’s woods, south of Farrar’s. It was on the end of a
limb about 20 feet from the ground.
Our notes have occasional references to both bumblebees and
honey bees. There is little bee-keeping about the lake (we saw a
few hives on the east side) though the country with its moist low-
lands covered with blossoms from early spring to late autumn
would furnish excellent cpportunities.
Lake Maxinkuckee, Physical and Biological Survey 41
THE MOLLUSKS
THE UNIONIDA
During the study of Lake Maxinkuckee considerable attention
was given to the mollusks, particularly the freshwater mussels or
Unionide. This was justified by the rapid and astonishing de-
velopment of the pearl button industry in America which is de-
pendent upon the shells of mussels for its raw material. The
recent discovery by Lefevre and Curtis of methods whereby com-
mercially valuable species of mussels are now successfully propa-
gated artificially, adds special interest to these mollusks. Recent
studies and discoveries relating to the formation and artificial pro-
duction of pearls in freshwater mussels may also be mentioned as
showing the importance of careful study of the taxonomy and life
history of the Unionide.
LAKES AND PONDS AS THE HOME OF MUSSELS
Generally speaking, lakes and ponds are not so well suited to
the growth and development of mussels as rivers are; the species
of lake or pond mussels are comparatively few, and the individuals
usually somewhat dwarfed. Of about 84 species of mussels re-
ported for the State of Indiana, only about 24 are found in lakes,
not all of these in any one lake, and several of them but rarely in
any. Of the 24 species occasionally found in lakes, but five are
reported only in lakes, and only three or four of the species com-
mon to both lakes and rivers seem to prefer lakes.
In rivers, the essential feature favorable to the development of
mussels is the current; and in the rivers the mussel beds reach
their best development in the riffles, whére the current is strong-
est. The importance of the current to the well-being of the
mussels is indicated by the position these mollusks naturally as-
sume in the beds, the inhalent and exhalent apertures of the crea-
tures being directed up-stream against the current. The im-
portance of the current is not merely as a bringer of food; exam-
inations show that the mussels of the plankton-rich lakes and
ponds usually contain more food material than those of rivers.
The current gives the river-mussels the advantage of a constant
change of water, which means a more abundant supply of oxygen,
and doubtless a more varied supply of mineral matter, from the
various sorts of soil through which the river flows.
The current is also probably of considerable importance in as-
sisting in the fertilization of mussels, one of its functions being
42 Lake Maxinkuckee, Physical and Biological Survey
the conveyance of sperm from mussels in upper portions of the
bed to other mussels below. In places where there is no current,
fertilization must be more largely a matter of chance.
Although the majority of species of mussels prefer a river
where there is a good current, some are more fitted to the quieter
parts of streams, or to ponds. These are chiefly thin-shelled spec-
ies with weakly developed or undeveloped hinge-teeth, best repre-
sented by the genus Anodonta. In some places Anodontas are
known as pond-mussels, as distinguished from the heavier sorts or
river-mussels.
The distinction between lakes and rivers is not constant in de-
gree; we have all sorts of gradations from the extreme form of
lake—isolated bodies without outlet—through lakes with relatively
large, important outlets, to such lakes as are simply expansions of
a river-bed, examples of the latter type being Lake Pepin, Minn.,
of the upper Mississippi, and the former English Lake in Indiana,
an expansion of the Kankakee. As a usual thing, the more fluvia-
tile a lake is, or the larger and more river-like its outlet, the more
river-like will be its mussel fauna, both in abundance and species.
In such lakes the mussels retain a vital continuity with the mussel
beds of the river. In the less fluviatile lakes the mussels are more
isolated, and there is more inbreeding. The large number (24)
of lake-dwelling species recorded for Indiana is due to the fact that
some of the lakes of Indiana are more or less fluviatile, and contain
several species of river shells.
ORIGIN AND CHARACTER OF THE MAXINKUCKEE MUSSELS
Lake Maxinkuckee, having a long, narrow, winding and rela-
tively unimportant outlet, is a representative of one of the less
fluviatile types of lakes, forming a pretty well marked contrast to
the various lakes cited above, and bearing a pretty close resem-
blance to the neighboring lakes, such as Twin Lakes, Pretty Lake,
Bass Lake, etc.
The Maxinkuckee mussels are doubtless derived from an-
cestors brought up the Outlet from the Tippecanoe River by as-
cending fishes. It is doubtful whether any have been introduced
by the numerous plants of fish in the lake, though such a thing is
possible. During the various times the lake was visited, a few
Tippecanoe River mussels were planted in the thoroughfare be-
tween the lakes, and a few Yellow River and Kankakee mussels
were planted in the main lake.
The Outlet of Lake Maxinkuckee is now a narrow, shallow
winding stream, straightened in places by ditching, and bordered
Lake Maxinkuckee, Physical and Biological Survey 43
on each side by a flat sedgy plain which indicates the former
breadth and importance of the stream. The colonization of the
lake with mussels was probably effected chiefly during the period
when the Outlet was a broad and relatively important stream.
The situation has been carefully considered and seems to show that
the mussels of the river and lake are isolated from each other and
that there is no longer any vital connection between them. The
strongest indication of the independence of the lake and river
mussel faunas is the appearance of the Maxinkuckee mussels them-
selves; these are lake-mussels, easily distinguished for the most
part from river mussels of the same species, and many of them are
ditinguishable also from the mussels of the neighboring lakes.
The Tippecanoe River is fairly well supplied with mussels. AI-
though the number of species is considerably fewer, and the size
of the individuals is generally smaller, than that of the Wabash
into which it flows, it compares very favorably with rivers of its
size. At Delong, Ind., a short distance above the mouth of the
Outlet of Lake Maxinkuckee, were obtained in one bed specimens
representing 24 species of mussels or about twice the number of
kinds found in Lake Maxinkuckee.
Our knowledge of the extent and importance of migrations of
fishes from the Tippecanoe River up to the lake and from the lake
down to the river—a question which has a marked bearing upon
the relationship of the mussel faunas—is not as complete as it
should be, but indications are that they are not important or ex-
tensive. Inasmuch as the geographic distribution of a given
species of mussel is coextensive with that of the species of fish
which serves as its host, this question is worthy of careful consider-
ation. There are severa! species of fishes of the Tippecanoe River
(Etheostoma camurum, Hadropterus evides, Hybopsis amblops,
etc.) which were not found either in the Outlet or in the lakes, and
other species (Hadropterus aspro, Ericymba buccata, Diplesion
blennioides) which have pushed halfway up the Outlet, but were
found no further up.
In this connection, the mussel fauna of the Outlet is worthy of
consideration, and on various occasions, but especially on a trip
down the Outlet September 30, 1907, particular attention was paid
to this feature.
The Outlet is not particularly well suited to the life and growth
of mussels; the bottom is either a firm peaty soil or fine shifting
sand ; moreover, the course has been artificially changed in some
places and the stream has naturally shortened its length in others
by making cutoffs. In addition to this the mussel fauna of such
44 Lake Maxinkuckee, Physical and Biological Survey
a narrow shallow stream would be the prey of muskrats, minks,
etc., the entire length and width of the beds.
On the trip mentioned above, about a mile below Lost Lake a
fine example of Lampsilis iris was found. This is the farthest up
stream any species of mussel was obtained, and as this species is
fairly common in both lakes and abundant in the Tippecanoe River,
we have here the nearest approach to a continuous fauna. Some
dead shells but no living examples of Quadrula undulata were
found a little farther down. Farther down stream, from a quarter
to half a mile, a short distance above the second cross-road south of
the lake, was found a small mussel-bed of about 40 or 50 mussels,
the great majority of which were Quadrula undulata. A few liv-
ing Lampsilis iris, two dead Symphynota compressa, one living
Symphynota costata (gravid), and a few dead shells of Quadrula
coccinea, complete the list. Below this point no mussels were
found until near where the Outlet joins the Tippecanoe. Here, a
few rods up the Outlet, a fair bed of Quadrula coccinea was found.
Of the five species of mussel found in the Outlet, only two, L. iris
and Q. coccinea, are found in the lake, the latter but rarely. The
form and general appearance of the Q. undulata of the Outlet is
quite peculiar and they can be picked out at once in collections
from the various rivers of the country. They are unusually elon-
gate, in this respect representing some of the Tippecanoe mussels
but differing from them in being thinner, and in having the fur-
rows between the plice unusually deep and sharp. The cost on
the postero-dorsal slope are very marked, and the epidermis jet
black. The umbones are considerably eroded.
DISTRIBUTION OF MUSSELS IN THE LAKE
In rivers, where there is a great variety of conditions, such as
differences of current, bottom, etc., one finds the different species
of mussels inhabiting different localities and different situations.
In the lakes, where we have comparatively few species of mussels
and not such important differences of environment, the distribu-
tion of the various species is much the same. The same condi-
tions, such as rather shallow water and moderately firm bottom,
are equally suitable for all. A few important exceptions may be
noted; as for example, the less common species of the lake are often
more or less local in distribution. The only well-marked bed of
Quadrula rubiginosa in the lakes is in the Lost Lake mussel-bed
below the Bardsley cottage, and this is the only place where Lamp-
silis subrostrata can be collected in any considerable numbers.
Lampsilis glans has a marked preference for the shallow water at
Lake Maxinkuckee, Physical and Biological Survey 45
the edge of the thoroughfare between the lakes; occasional ex-
amples can, however, be picked up almost anywhere along shore,
and it appears to be increasing considerably along shore at Long
Point. Anodonta grandis footiana, which can live in softer bottom
than the other mussels, has a considerably wider distribution, and
was dredged up in deeper water than any of the other mussels.
The mussels are to be found almost anywhere in water from
2 to 5 or 6 feet deep where the bottom is more or less sandy or
marly. The beds are composed chiefly of the three principal spec-
ies of the lake, Lampsilis luteola, Unio gibbosus and Anodonta
grandis footiana, with the less common species sparsely inter-
spersed. Especially good mussel beds occur at Long Point, along
shore by Farrar’s and McDonald’s, by the Depot grounds, in
Aubeenaubee Bay out from the Military Academy, and in the shal-
low water just beyond the mouth of Norris Inlet. Mussels are
fairly well scattered from Long Point more or less continuously all
the way southward to beyond Overmyer’s hill, and from a little
north of the ice-houses all the way around to the Military Academy.
They are quite abundant in the neighborhood of Winfield’s in shal-
low water, and occur scattered along the east side of the lake a
little way out from shore. A good mussel bed is found in Lost
Lake along the east shore, extending from a little south of the
Bardsley cottage to where the bulrushes and water-lilies grow
thickly in the soft black muck near shore.
Movements:—Closely connected with the question of distribu-
tion is that of movement. The greater number of mussels of the
lake, especially in the deeper water, spend their lives in a state of
quiescence. Young mussels appear to be more active than older
ones. The mussels retain the power of locomotion during all their
lives, but after they have got well settled down, they only occa-
sionally use this power. The mussels of the shallow water near
shore move out into deeper water at the approach of cold weather,
in late autumn or early winter, and bury themselves more deeply
in the sand. This movement is rather irregular and was not ob-
served every year. It was strikingly manifest in the late autumn
of 1913, when at one of the piers off Long Point a large number of
furrows was observed heading straight into deep water with a
mussel at the outer end of each. The return of the mussels to
shore during the spring and summer was not observed. Many of
them are probably washed shoreward by strong waves of the spring
and summer storms, and some are carried shoreward by muskrats
and dropped there. Occasional mussels were observed moving
about in midwinter—even in rather deep water. During the
46 Lake Maxinkuckee, Physical and Biological Survey
winter of 1900-1901 an example of Lampsilis luteola, in rather
deep water in the vicinity of Winfield’s, was observed to have
moved about 18 inches within a few days. Its track could be dis-
tinctly seen through the clear ice.
As a result of the quiescence of the lake mussels, the posterior
half or 4 of the shell, which projects up from the lake bottom, is
usually covered by a thick marly concretion which appears to be
a mixture of minute algz and lime. This marly concretion grows
concentrically, forming rounded nodules, its development increas-
ing with the age and size of the shell. This concretion, though
most abundant on shells, is not confined entirely to them, but grows
also on yocks that have lain undisturbed on the bottom. When
growing on shells, it adheres to them very closely; and upon being
pried loose sometimes separates from them much as the matrix
separates from a fossil, and leaves the epidermis of the mussel
clean. In other cases it adheres more firmly and is difficult to
scrape off clean. On this marly growth, colonies of Ophrydium,
much the size, color, and general appearance of grapes with the
skins removed, are often found growing, and in the cavities and
interstices of the marl, a handsome little water-beetle, Stenelmis
undulatus Blatchley, and its peculiar elongate black larve, live in
considerable numbers but apparently have nothing to do with the
mussels. Various species of hydrachnids, one of them strikingly
handsome with its green body sprinkled with bright red dots, also
live in the cavities of the marl, and offer some suggestion as to
how the parasitic mite Atax went a step farther and took up its
habitation within the mussel itself.
Food and feeding:—An examination of the stomach and in-
testinal contents of the various species of mussels of the lake ~
showed no noticeable differences between the food of the different
species. Enough of the bottom mud is generally present to give
the food mass the color of the bottom on which the mussels are
found; thus the stomach-contents of the mussels found in the
black bottom of Lost Lake was usually blackish, while that of
those found in the lighter bottom at Long Point was grayish. In-
termixed, however, with the whole mass was always enough algee
to give it a somewhat greenish tinge, this green being usually inter-
mixed more or less in the form of flakes. The plants had sprouted up well by May 24. There
was a large robust patch along a ditch beside the road near
Ferrier’s lumber yard. The leaves of these were peculiarly
blotched with white splashes, some more than others, but nearly
all thus marked to some extent. Other plants along the shore of
the lake near the Merchants’ pier were splashed with purple
blotches on the upper sides of the leaves. Selection among the
most strongly marked plants of both of these series would prob-
ably result in handsome and variegated plants. Even the un-
marked plants are highly worth a place at the borders of orna-
mental ponds. The Chinese use a plant very similar to our broad-
leaved arrowhead as a house plant simply for foliage effects.
49. GRASS-LEAVED SAGITTARIA
SAGITTARIA GRAMINEA Michx.
There was a patch of this plant along the east side of Lost Lake
below the Bardsley cottage, and some in the large lake near Norris
Inlet, and down aiong the outlet.
The plant varies considerably in appearance and behavior ac-
cording to location. The patch in Lost Lake grew in 2 or 3 feet
of water, and the lower leaves formed attractive close rosettes,
closely resembling those of Eriocaulon. These plants blossomed
but rarely. They propagated by stolons, and the leaves stayed
green under the water all winter. In the winter of 1904, much
was pulled up in Lost Lake and washed ashore. It was probably
pulled up by muskrats. The plants bear spherical tubers which
that animal probably uses for food.
The plants along shore of the lake near the old ice office and in
front of the Assembly grounds bloomed quite profusely in 1906
and in succeeding years. Both circles of the perianth segments
were conspicuous, crisped and crinkled, and of a delicate rosy hue,
so that each blossom looked like a double flower. They were ex-
ceedingly attractive, and well worthy of cultivation.
iw)
iS)
i
Lake Maxinkuckee, Physical and Biological Survey
FAMILY 14. VALLISNERIACEH. 'TAPE-GRASS FAMILY
50. DITCH-MOSS
PHILOTRIA CANADENSIS (Michx.) Britton
The ditch-moss is fairly common in the lake in shallow water.
In rich muddy bottom it forms a rank, thick growth, while in sand
it grows more sparsely and not so large. Among the places where
it was noted growing was in shallow water between the gristmill
and elevator, at the Merchants’ pier where it grew quite rank, by
the green boathouse near Norris Inlet, by the icehouses, near
Farrar’s, in front of the Assembly grounds, near the head of the
thoroughfare between the lakes, etc. In recent years it has begun
growing in immense dense patches at Long Point near Chadwick’s.
This appears to be a new location for it. It also forms dense tall
masses in Culver Inlet in the Academy grounds.
This plant is remarkably variable in form, as regards leaf ar-
rangement and leafiness, and bud variations in this respect are
quite common. Although the leaves are usually in 3’s and rather
remote on the stem, there are sometimes branches in which the
leaves are closely crowded in whorls of 5 or 6 making a dense cone.
This may function at times as a propagating bud but it does not
appear to be a usual winter bud form as they often form
early in the season and sometimes lengthen again, apparently, be-
fore winter. It seems to be really a different form of the plant,
as some plants once seen in a river were all of this dense form. We
have notes of this having been found in flower as early as June 24.
The blossoms, dainty rose tinted objects on an exceedingly slender,
hair-like long tube, are quite common during the autumn. Al-
though plants near shore appear to die down, the deeper water
patches remain green all winter.
Although this water-weed is a bright, clean-looking, attractive
plant, one of the most ornamental in the lake, nothing appears to
feed on it. It is said to have become a great nuisance in the
streams and rivers of Europe where it is known in places as “water-
pest”. Where it grows in great masses it might be raked out and
used as compost, though in drying out it shrivels almost to nothing,
leaving very little substance for the amount of material handled.
Plants noted in the autumn of 1913 had the leaves well coated
with a deposit of lime.
222 Lake Maxinkuckee, Physical and Biological Survey
51. TAPE-GRASS; EEL-GRASS; WILD CELERY
VALLISNERIA SPIRALIS L.
During 1900 and 1901, eel-grass was noted as rather common
in the lake, usually growing in small scattered patches. It grew
rather tall and rank in muddy bottom, and dwarf plants grew
thinly on sand. Among places where it was observed were: the
Weedpatch, a rather thick patch along the east shore of Long
Point as along by McSheehy’s, Duenwig’s and Darnell’s, along the
depot grounds; in front of the Palmer house, by Farrar’s, a long
broken patch from the Assembly grounds pier to Kreutzberger’s
pier, and at the head of the thoroughfare. It grew in the thor-
oughfare between the lakes and was rather common in Tippecanoe
River into which the outlet of the lakes flows. It was found grow-
ing down to a depth of 9 feet.
It is a favorite food of the coot and ducks; the rootstock puts
out a delicate white stolon in autumn as a starter for the next year’s
growth. It appears to be this portion that the ducks are especially
fond of. Soon after the water-fowl arrive, torn up plants of this
species are washed up in great rolls along shore, they probably
having been pulled up by these birds. During the first years of
the survey but few flowers and no fruit were observed. The
patches nearly all disappeared before the ducks left, and the
plants hardly seemed to be holding their own. Of late years
this species appears to be rapidly gaining and spreading. Blos-
soms of both sexes became very abundant. In 1906 from July
30 to September 6, the surface of Outlet Bay was frequently densely
covered by the staminate blossoms which in places formed a regular
scum. The same phenomenon was noted in succeeding years
(1907, 1908, 1909 and 1913). The blossoms would frequently be
gathered in clumps around floating objects, especially around the
pistillate flowers. Considerable patches of the pistillate plants
were observed in places with their conspicuous light-colored curious
spiral stems as they withdrew into deeper water after being fer-
tilized. The fruits are becoming common objects in the lake. They
are peculiar, elongate, obtusely triangular green pods, very muci-
laginous and with a sprightly acid taste.
In the autumn of 1906, a very narrow but strikingly dense
and long patch was found growing in water five or six feet deep
near the Merchants’ pier. Its luxuriant growth and small area ex-
cited our interest, and, upon dredging it up, it was found to be
growing in an old bait-can which had sunk at that place.
Lake Maxinkuckee, Physical and Biological Survey 223
Most of the leaves, especially the long ones, appear gradually
to die in late autumn, first turning reddish and then bleaching out
to a dead white. Some green leaves can be raked up all winter,
however. The green leaves late in the season are frequently coated
with colonies of a small white Vorticella and, oddly enough, the
whitened leaves are similarly coated with a green Vorticella.
The little mollusk Ancylus is frequently found on the leaves of
this plant, especiaily near the base. The only other place it was
found was occasionally attached to the outside of the shell of
Viviparus.
The increase of this, as well as other plants in the lake, is prob-
ably due to the more active hunting of water-fowl, which gives the
plants a better opportunity to thrive.
FAMILY 15. GRAMINEZ. GRASS FAMILY
52. BROOM BEARD-GRASS
SCHIZACHYRIUM SCOPARIUM (Michx.) Nash
The broom beard-grass, generally known throughout the state
as broom-sedge, is usually found only on barren sandy slopes. It
is a coarse rough tussocky grass. It hardly attracts attention dur-
ing the summer, but in late autumn its scattered clumpy growth,
the harshness of its outline, and the sereness of its brown re-
lieved only by the feathery tufts of its plumed seed, scattered
scantly along the stem, all unite to make the regions where
it grows especially desert and desolate. There were a few
areas on the slope about the lake where it grew. The hill near
shore south of McOuat’s was almost covered with it, and some grew
south of the Plank cottage, a little grew by Murray’s, and some
south, along the railroad.
538. FORKED BEARD-GRASS
ANDROPOGON FURCATUS Muhl.
This grass differs considerably in appearance and habits from
the preceding. It is a tall, rather handsome grass, with a stiff
wiry culm, the inflorescence on diverging narrow spikes like those
of the crab-grass, only on a larger scale. Coulter, in his report
on the plants of the state, says that it is “a common form on prairie
soil, either moist or dry, where it furnishes a large amount of hay.”
In the neighborhood of the lake it grows in small scattered clumps
in open places in dry soil and is not abundant enough to be made
use of. It occurs both east and west of the lake.
224 Lake Maxinkuckee, Physical and Biological Survey
54. INDIAN-GRASS; WOOD-GRASS
SORGHASTRUM NUTANS (L.) Nash
This tall handsome but rather coarse grass grows in scattered
clumps in rather open places about the lake. The oat-like appear-
ance of the panicle, and the bright shining yellow of the transpar-
ent glumes through which the stamens show, make it an easily rec-
ognizable and attractive grass. In our area it never forms con-
tinuous patches.
55. SLENDER FINGER- OR CRAB-GRASS
SYNTHERISMA FILIFORME (L.) Nash
Rather common in dry sandy soil but not so conspicuous as the
next on account of its small size. It flowers in August and Sep-
tember.
56. LARGE CRAB-GRASS
SYNTHERISMA SANGUINALE (L.) Dulac.
Too common in cultivated fields about the lake. It is not
troublesome in cornfields and meadows, but in low cultivated crops
such as gardens, and particularly in potato fields, the wiry prostrate
stems which root at the nodes soon form a very tough compact sod,
difficult to remove from the soil. It begins blossoming late in
summer, and continues putting out spikes of blossoms until killed
by frost.
57. BARNYARD GRASS; COCKSPUR-GRASS
ECHINOCHLOA CRUS-GALLI (L.) Beauv.
This is a well-known grass throughout the state, usually quite
common in rich moist ground. Its favorite habitat is the flat
marshy shores of rivers and creeks, and the corners of neg-
lected barnyards where the seepage from manure piles keeps the
ground moist. In the vicinity of Lake Maxinkuckee this plant is
confined mostly to a narrow belt along shore where it is one of the
most common of the beach plants. Very little is found any
distance from the lake on account of the dry sandy nature of the
soil.
The Cockspur Grass never cover's extensive areas, even over flat
moist places, but prefers narrow edges along streams. In favor-
able situations it forms a very leafy rank growth and would prob-
ably furnish considerable forage or hay. An enterprising western
seedsman boomed it extensively as “Billion dollar grass’, a new and
wonderful “introduction from Japan”, but the boom seems to have
Lake Maxinkuckee, Physical and Biological Survey 225
subsided. One of the chief difficulties with the grass is that it is
an annual, producing a single crop to the sowing, and would have
to be handled much like millet.
58. SALT-MARSH COCKSPUR-GRASS
ECHINOCHLOA WALTERI (Pursh) Nash
This is not so common as the preceding, only a few plants hav-
ing been found along the southwestern shore of the lake, inter-
mixed with the other species. It is fairly common along the shore
of Yellow River near Twin Lakes. This species is generally more
robust and of a deeper purple color than EL. crus-galli, and usually
has much longer awns. On account of its more robust habit, it
would make a more promising pasture or meadow grass than the
other unless its roughness and beardiness proved a serious draw-
back.
59. WITCH-GRASS; TUMBLE-WEED
PANICUM CAPILLARE L.
While fairly common in places, this grass is not so abundant in
the neighborhood of the lake as in many other parts of the state.
It is rather frequent along the beach, especially by the railroad
bridge at Culver. It was found also on the first and second ter-
races of the beach at Long Point, and along the shore by Scovell’s
and Arlington. It was common in cultivated grounds east of the
lake. Most of the plants found in the vicinity of the lake were
small and dwarfed, and it does not form a conspicuous feature of
the landscape.
The old witch-grass thrives most luxuriantly in rich black soil,
either in tilled ground or in meadows and pastures where the sod
has been killed out. A luxuriant patch has a peculiar airy fineness
about it which gives it an unique charm. Before it has ripened, the
rich purple of the fine spray-like heads gives the effect of a distant
haze to landscapes near at hand. A very fine effect of this sort
was observed along the Vandalia railroad several miles above Cul-
ver, where there was a large patch. When ripe and dead, a dense
patch, hiding the ground beneath with its mist-like fineness, gives
the appearance of a cloud; to walk through it gives a sense of in-
security,—it is almost like walking on air. When each of the tiny
sprigs holds a minute drop of dew or fog on a gray morning, the
effect is quite indescribable.
Well developed plants in rich ground form great globular masses
somewhat like the winged pigweed, the cultivated Kochia, or the
15—17618—Vol. 2
226 Lake Maxinkuckee, Physical and Biological Survey
Amaranth. Other tumble-weeds of the plains, except the witch-
grass globes, are much finer and more airy. These, after ripening,
break off at the base and scud before the autumn winds like fright-
ened rabbits. The sight of one of these delicately formed globes
rolling before the fitful autumn blasts, scattering seed as it goes, is
another revelation of the attractive and surprising features of this
plant. In some parts of the state, especially the flat rich prairies
along the middle of our western boundary, this species forms
great masses like snow-drifts against fences or hedges, and fills up
open ditches.
60. TALL SMOOTH PANICUM
PANICUM VIRGATUM L.
A rather coarse, leafy grass growing in clumps or tussocks. The
amount of material in a single clump suggests that it might make
considerable forage where abundant enough. Its tussocky habit of
growth, however, is somewhat against it. It is noteworthy for the
deep red color of its pollen. The plants first come into flower about
the latter part of July.
It was not originally common at the lake, only a few clumps
having been noted along the road below the Duenweg cottage at
Arlington. It appears to be increasing considerably of late years,
as numerous clumps now grow along the road between the lake and
Culver. In the particular plant examined the sterile flowers were
rudimentary.
61. BARBED PANIC-GRASS
PANICUM MICROCARPON Muhl.
One of the broad-leaved panicums growing in the sandy soil of
open woodlands, fairly common in the dry soil west of the lake.
This plant is small and compact at the beginning of the flowering
season. It continues to grow all the season, putting out new
panicles from the sheaths of successively lower leaves so that in
the end we have a very diffuse spraggly plant with empty panicles
from which the seed have been shed, ripening grain in all stages of
development, flowers and buds all at the same time. The grass is
too small and scattered to be of any importance as pasturage.
62. SCRIBNER’S PANIC-GRASS
PANICUM SCRIBNERIANUM Nash
In general habit much resembling P. microcarpon; blossoming
all season and becoming quite diffuse late in autumn. Found in
open sandy soil west of the lake.
Lake Maxinkuckee, Physical and Biological Survey 227
63. VELVETY PANIC-GRASS
PANICUM SCOPARIUM Lam.
Not rare in dry open ground on the west side of the lake be-
tween Long Point and Arlington. Collected in flower June 26,
1901. One of the inconspicuous grasses of the region.
64. YELLOW FOXTAIL; PIGEON-GRASS
CHAETOCHLOA GLAUCA (L.) Scribn.
Rather common in waste places, and along the shore of the lake
at the railroad bridge at Culver.
65. GREEN FOXTAIL-GRASS
CHAETOCHLOA VIRIDIS (L.) Scribn.
Somewhat common in waste places, and along the railroad.
Through many parts of the state this is one of our most vexatious
and troublesome weeds. The seeds germinate almost any time dur-
ing the summer. We found it in flower along the railroad June
26, which is unusually early. Where most abundant it usually
springs up in cornfields and potato patches after cultivation has
ceased, and makes the harvesting of these crops difficult. In gen-
eral it is not so prominent in the weedy autumn fields as formerly,
its place having been taken by ranker, broad-leaved weeds.
66. HUNGARIAN GRASS; MILLET
CHAETOCHLOA ITALICA (i) Seribn.
This is frequently cultivated, and occasionally escapes. It does
not usually persist very long, however. A patch at Long Point at-
tracted various birds and seed-eating mammals to that place. Some
of the 13-lined gophers, which had previously been confined largely
to the Gravelpit along the railroad, found the place attractive and
made their homes there in 1906. A few snow buntings or snow-
flakes appeared to light by chance and, finding good feeding in this
patch of millet, brought others from somewhere, the flock gradually
increasing until there were 25 or 30 birds. They had not been
noted in the vicinity previously.
Besides the Long Point patch, some was also noted east of the
lake.
67. SMALL BUR-GRASS
CENCHRUS CAROLINIANUS Walt.
This is undoubtedly the most pestiferous weed in the neighbor-
hood of the lake. It is frequent along the lake shore and common
along the railroad, but is in neither of these places so abundant as
228 Lake Maxinkuckee, Physical and Biological Survey
to be a great nuisance. It reaches its maximum abundance in the
sandy fields along the east side of the outlet of Lost Lake, and here
it is abundant enough at times to make passage through the fields
quite vexatious. The grass comes up in spring, handsome and in-
viting, and suggests good pasturage, and the small grain within the
bur is pleasant in taste and texture, somewhat resembling rice; but
even at the best, little good can be said of this plant, and the
principal problem is its extinction. The burs become conspicuous
about the middle of July, but it is after they have ripened that they
are especially obnoxious.
68. WILD RICE
ZIZANIA AQUATICA L.
With the possible exception of the reed, Phragmites, the wild
rice when well developed, is one of the most handsome of our native
grasses. Its tall stately appearance, the rich golden yellow of its
widely spreading staminate flowers which droop gracefully around
the sides of the panicle, contrasting with the stiff erect pyramidal
heads of pistillate flowers, make the first sight of these plants one
to be long remembered. Each looks like a vegetable fountain, with
a straight silvery jet in the center, the outer circle of spray toward
the base sparkling in the sunlight. It is not very abundant in
the vicinity of the lake.
Melasoma, 33, 34.
Interrupted Pondweed, 178.
interruptus, Potamogeton, 178.
interstincta, Eleocharis, 188, 241.
intertextus, Viviparus, 75.
inundatum, Lycopodium, 207.
Tonactis linariifolius, 456.
Ipomoea pandurata, 347, 396.
irene, Nehalennia, 21.
Iridacez, 268.
Iris Family, 268.
Iris versicolor, 268.
iris, Lampsilis, 44, 61.
Iron-weed, Tall, 427.
Western, 427.
Iron-wood, 281.
irritabilis, Opercularia, 98, 99.
irrorata, Notonecta, 30.
Ischnura kellicotti, 23.
verticalis, 23.
Isnardia palustris, 371.
Isopods, 78.
Isopyrum biternatum, 309.
italica, Chaetochloa, 277.
Ivy, Ground, 403.
Poison, 354.
Three-leaved, 354.
Ivy-leaved Duckweed, 166, 257.
482
Jack-in-the-pulpit, 253.
Jackson Park, Chicago, 424.
Japanese Clover, 343.
jenneri, Spirulina, 1438.
Jerusalem Oak, 297.
Jewel-weed Family, 349.
Jimson-weed, 408.
Joe-pye Weed, 428.
Johannsen, Dr. O. A., 7.
Johnny-jump-up, 369.
jubatum, Hordeum, 238.
Judas-tree, American, 337.
Juday, Chancey, 76, 105, 113.
Juglandacesx, 272.
Juglans cinerea, 272.
nigra, 272.
Juncacee, 261.
juncea, Solidago, 431.
junceus, Aster, 434.
Juncoides campestre, 262.
Juncus acuminatus, 262.
brachyearpus, 262.
bufonius, 261.
canadensis, 262.
effusus, 261.
nodatus, 262.
tenuis, 261.
June-berry, 335.
June-grass, 237.
Juniperus virginiana, 209.
junius, Anax, 24, 25.
kalmii, Lobelia, 423.
Kalm’s Lobelia, 4238.
Kankakee marshes, 258, 295.
Kankakee River, 42, 51, 56, 78, 285,
366.
Kansas Tumbleweed, 297.
Katydids, 27, 28.
Keithsburg, IIll., 349.
Kellicott, Claus and, 79.
kellicotti, Ischnura, 23.
Kellogg, Prof. Vernon L., 31.
Kentucky Blue-grass, 237.
Coffee-tree, 338.
Ketmia, Bladder, 366.
Kewanna, Ind., 209.
Kidney-leaved Crowfoot, 312.
King-nut, Big, 275.
kirklandi, Ancylus, 73.
Kneiffia pumila, 373
ole.
Lake Maxinkuckee, Physical and Biological Survey
Knot-grass, 293.
Knotweed, Erect, 293.
Slender, 2983.
Virginia, 294.
Knotted Spike-rush, 188, 241.
Knox, Ind., 297, 298, 390.
Kochia scoparia, 297.
Koellia flexuosa, 405.
virginiana, 405.
Krigia virginica, 423.
Kuetzingianum, Coelosphaerium, 142.
Kyllinga, Low, 239.
pumila, 239.
Labiate, 402.
Labidesthes sieculus, 100.
Labrador Pine, 207.
labrusea, Vitis, 362.
labyrinthica, Strobilops, 75.
Lace Bug, 30.
Plant, 381.
Queen Anne’s, 381.
lacera, Blephariglottis, 270.
lacerata, Tramea, 24, 26.
Lacinaria pyconostrachya, 429.
seariosa, 429.
spicata, 429.
laciniata, Dentaria, 320.
Rudbeckia, 438.
lacustrinum, Pisidium, 74.
lacustris, Ceriodaphnia, 107.
Epischura, 107.
Lactuca hirsuta, 425.
spicata, 425.
villosa, 425.
virosa, 424.
lactuosa, Libellula, 11, 13, 16, 17, 18.
lactuosus, Gryllus assimilis, 29.
Ladona exusta, 26.
Lady-fern, 203.
Ladies’-slipper, Showy, 269.
Ladies’-tresses, Nodding, 270.
Lady’s Thumb, 294.
laevigata, Arabis, 319.
Dasystoma, 412.
laevigatum, Equisetum, 206.
levigatus, Pisidium compressum, 74.
laevis, Aster, 434.
Bidens, 441.
Lake Amelia, Minn., 47.
Lake Maxinkuckee, Physical and Biological Survey 483
Lake, Bass, 18, 14, 17, 42, 56, 65, 112, lanuginosa, Hypopitys, 285.
116, 184, 245, 260, 275, 288, 305, lapathifolia, Persicaria, 294.
32), Gel, che, Bie, 4sul, dae. Lappula lappula, 399.
Champlain, 70, 79. virginiana, 400.
Chapman, 112. lappula, Lappula, 399.
Cedar, 56, 198. Larch, American, 208.
Center, 56. Large Blue-fiag, 268.
Cicott, 305. Button-snakeroot, 429.
County, Ind., 193. Crab-grass, 224.
Deedes, Ho, 1s, hl PG BRB. Rol Cranberry, 387.
PADIS, Bi), Bel), 4alat. Panacled Sedge, 250.
English, 42. Spotted Spurge, 351.
Erie, 65. White Wild Indigo, 338.
Fletcher, 189, 240, 244, 248, 408. Yellow Pond Lily, 304.
Pepin, Minn., 42. Large-bracted Plantain, 417.
Phalen, 30. Tick-trefoil, 342.
Pokegama, Minn., 65, 113, 167. Verbena, 401.
Pretty, 42, 56. Large-flowered Bellwort, 266.
Tippecanoe, 62, 72. Sensitive Pea, 338.
Upper Fish, 56, 63. Large-leaved Aster, 433.
Winona, 310, 311. Pondweed, 171, 212.
Lake-of-the-Woods, 56, 112, 200, 209, Large-mouthed Black Bass, 11, 80.
261, 288, 305, 360, 4438. Large-toothed Aspen, 376.
Lakes and ponds as the home of Mus- Larger Bur-marigold, 441.
sels, 41. Indian Bean, 416.
Lakes, Fish, 325. Mouse-ear Chickweed, 300.
Twin, 13, 14, 16, 17, 37, 42, 49, 56, laricina, Larix, 208.
65, 111, 112, 180, 247, 258, 276, Larix laricina, 208.
305, 318, 376, 414. Late Golden-rod, 431.
Lamb’s Quarters, 297. Purple Aster, 433.
Lampsilis fallaciosa, 63. lateriflora, Scutellaria, 402.
glans, 44. Lathyrus palustris, 344.
iris, 44, 61. venosus, 344.
luteola, 34, 45, 46, 48, 65, 101, 149. latifolia, Sagittaria, 219.
luteola, food of, 67. Silene, 300.
multiradiata, 48, 71. Typha, 191, 210.
subrostrata, 44, 63. latum, Cosmarium, 152.
subrostrata, food of, 64. Lauracee, 315.
ventricosa, 48, 49, 69. Laurel Family, 315.
Lampyrids, 34. Lead-plant, 341.
lanatum, Heracleum, 378. Leaf, Velvet, 365.
Lance-leaved Violet, 369. Leather-flower, 314.
lanceolata, Pedicularis, 413. Leather-leaf, 386.
Plantago, 417. Leather-wood, 370.
Viola, 369. Lechea minor, 368.
lanceolatum, cirsium, 446. lecontei, Psephenus, 33, 34.
Land Flora, 124. Leeches, 87.
Introduction to, 124. Leek, Wild, 262.
Land Mollusks, 74. Lecticula resupinata, 415.
landsboroughii, Gidogonium, 157. Lefevre and Curtis, 41.
lanuginosa, Carex, 253. leidyi, Meyenia, 104.
484
Lemnacez, 256.
Lemna minor, 167, 258.
perpusilla, 167, 258.
trisulea, 166, 257.
lentago, Viburnum, 420.
Lentibulariacee, 413.
Leontodon taraxacum, 424.
Leonurus cardiaca, 404.
Lepidium virginicum, 318.
Lepidoptera, Order, 37.
Lepomis pallidus, 80.
leporella, Scrophularia, 409.
leptalea, Carex, 251.
Leptamnium virginianum, 415.
Leptandra virginica, 412.
Leptilon canadense, 436.
Leptodora hyalina, 77, 107, 108.
leptostachya, Phryma, 415.
leptostachys, Lobelia, 423.
Lespedeza capitata, 343.
hintass4ee
striata, 343.
violacea, 343.
virginica, 343.
Lesser Bladderwort, 196, 414.
Duckweed, 167, 258.
Panicled Sedge, 250.
Lestes congener, 26.
forcipatus, 20.
unguiculatus, 19.
vigilax, 20.
Leticula resupinata, 192.
Lettuce, Hairy-veined Blue, 425.
Prickly, 424.
Tall Blue, 425.
White, 425.
leucantha, Baptisia, 338.
leucanthemum, Chrysanthemum, 445.
leuchtenbergianum, Diaphanosoma,
ie
leuckarti, Cyclops, 77, 107.
leucophaea, Blephariglottis, 270.
Leucorhinia intacta, 15.
Libellula cyanea, 17, 26.
incesta, 17, 26.
lactuosa, 153, 16.1 7 als,
pulchella, 11, 16, 26.
quadrimaculata, 17.
Libythea bachmani, 39.
Lichen, Bearded, 376.
liebleinii, Schizomeris, 156.
Lake Maxinkuckee, Physical and Biological Survey
Life Everlasting, Fragrant, 437.
Liliacezw, 262.
Lilium canadense, 263.
superbum, 263, 264.
umbellatum, 263.
Lily Family, 262.
Lily Family, Water, 304.
Lily, Large Yellow Pond, 178, 304.
Pond, 180.
Sweet-scented White Water,
305.
Turks-cap, 264.
Western Red, 263.
Wild Yellow, 263.
Lily-of-the-valley Family, 265:
Lily-of-the-valley, False, 265.
limi, Umbra, 258.
Limnanthacee, 349.
Limodorum tuberosum, 270.
limosa, Amnicola, 73.
porata, Amnicola, 73.
Linacee, 349.
Linaria canadensis, 409.
linaria, 409.
linaria, Linaria, 409.
linariifolius, Ionactis, 436.
Linden Family, 364.
Linden, American, 364.
Linear-leaved Willow-herb, 372.
lineare, Epilobium, 372.
lineatus, Scirpus, 248.
Linseed, 349.
Linum usitatissium, 349.
Liparis loeselii, 271.
Liquidambar styraciflua, 325.
Liquorice, Wild, 419.
Liriodendron tulipifera, 305.
Lithospermum canescens, 400.
ecarolinense, 400.
Little River, 78.
Live-forever, 322.
Liver-leaf, Round-lobed, 310.
Liverwort, Round-lobed, 310.
Sharp-lobed, 311.
livescens, Goniobasis, 73.
Livid Willow, 280.
livida, Comandra, 291.
lividus, Gomphus, 25.
Lizard-tail Family, 272.
Lizard’s-tail, 272.
lobata, Micrampelis, 421.
180,
Lake Maxinkuckee, Physical and Biological Survey 485
Lobeliacew, 423. Low Hairy Ground-cherry, 407.
Lobelia Family, 423. Kyllinga, 239.
Lobelia cardinalis, 423. Nut-rush, 249.
kalmii, 423. Rose, 333.
leptostachys, 423. Spear-grass, 236.
syphilitica, 4238. Low-running Blackberry, 332.
Great, 423. lubrica, Cochlicopa, 75.
Kalm’s, 423. Tetraspora, 149.
Spiked, 4258. lucens, Potamogeton, 176.
Locust, Dog-day, 31. lucida, Salix, 279.
Locust-tree, 341. luctuosa, Libellula, 16.
loeselii, Liparis, 271. Ludwigia alternifolia, 372.
Loesel’s Twayblade, 271. polycarpa, 372.
Logansport, Ind-, 189, 271. Many-fruited, 372.
longatum, CGidogonium, 157. Lupine, Wild, 339.
Long-branched Frostweed, 367. Lupinus perennis, 339.
Long-fruited Anemone, 310. lupulina, Carex, 253.
Long-leaved Pondweed, 176, 213. Medicago, 339.
Rush-grass, 231. lupulus, Humulus, 290.
Stitchwort, 300. lustrica, Amnicola, 73.
Long-spurred Violet, 370. luteola, Lampsilis, 34, 45, 46, 48, 49,
Long-stalked False Pimpernel, 410. 65, 101.
longifolia, Alsine, 300. lutescens, Riccia, 380.
longipennis, Pachydiplax, 16. lutetiana, Circaea, 374.
longipes, Emesa, 30. Lycenopsis pseudargiolus, 39.
longissima, Synedra, 164. Lycopodiacex, 207.
longistylis, Washingtonia, 378. Lycopodium inundatum, 207.
Lonicera oblongifolia, 421. Lycopus americanus, 405.
Looking-glass, Venus’, 422. lydia, Plathemis, 18.
Loosestrife Family, 370. Lymnea dalli, 72.
Loosestrife, False, 372. danielsi, 72.
Bulb-bearing, 388. desidiosa, 72.
Fringed, 388. humilis, 72.
Swamp, 191, 370. obrussa exigua, 72.
Tufted, 389. palustris, 72.
Whorled, 388. Lyngbya estuarii, 144.
Wing-angled, 371. Lysimachia quadrifolia, 388.
Lopseed Family, 416. terrestris, 388.
Lopseed, 416. Lythracee, 370.
Lost Lake, Aquatic Plants of, 192. Lythrum alatum, 371.
louisvillensis, Goniobasis, 73.
Lousewort, 413. macrocarpa, Quercus, 286.
Swamp, 413. macrocarpus, Oxycoccus, 387.
Love Vine, 397. macroceras, Ceratium, 97.
Love-grass, Pursh’s, 235. macrorhiza, Utricularia, 198, 414.
Small Tufted, 234. maculata, Calopteryx, 18.
Smooth Creeping, 236. Chamaesyce, 351.
Strong-scented, 234. Cicuta, 381.
Low Blueberry, 387. Cymbella, 163.
Birch) 28e. maculatum, Geranium, 348.
Cyperus, 240. maculosus, Argulus, 79.
486 Lake Maxinkuckee, Physical and Biological Survey
Mad-dog Skulleap, 402. Marrubium vulgare, 402.
Madder Family, 417. Marsh Arrow-grass, 219.
Madder, Wild, 419. Bed-straw, Stiff, 419.
magma, Gloeocapsa, 141. Bellflower, 422.
Magnolia Family, 305. Cinquefoil, 330.
Magnoliacee, 305. Foxtail, 231.
Maiden-hair Fern, 205. Holy Rose, 886.
mainense, Pisidium, 74. Milkwort, Cross-leaved, 350.
major, Eragrostis, 235. Muhlenbergia, 230.
Oscillatoria, 144: Purslane, 371.
Plantago, 416. Shield-fern, 201.
majuscula, Spirogyra, 154. St. John’s-wort, 367.
Malacex, 334. Skulleap, 402.
Mallard, 295. Speedwell, 411.
Mallow-Family, 364. Trefoil, 392.
Mallow, Common, 364. Vetchling, 344.
European, 365. Water-cress, 317.
False, 365. Marsh, Prof. C. Dwight, 107.
Indian, 365. Marsh-grass, Tall, 233.
Malus glaucescens, 334. Marsh-marigold, 309.
malus, 334. Marshes, Kankakee, 295.
malus, Malus, 334. Maryland Figwort, 409.
Malvacee, 364. marylandica, Meibomia, 348.
Malva alcea, 365. Sanicula, 377.
rotundifolia, 364. Scrophularia, 409.
Man-of-the-earth, 396. mas, Cornus, 324.
Mandrake, Wild, 315. Mat-rush, 185, 246.
Mann, Dr. Albert, 140, 161. Maumee River, 49, 62, 78, 118, 361.
Manna-grass, Floating, 237. Maxinkuckee Mussels, 42.
Nerved, 237. May Apple, 315.
Many-flowered Agrimony, 331. May-flies, 8.
Many-fruited Ludwigia, 372. Mayflower, 386.
Maple Family, 356. Mayweed, 444.
Maple, Ash-leaved, 360. meadia, Dodecatheon, 389.
Hard, 360. Meadow Bitter-cress, 320.
Red, 359. Blue Violet, 369.
Silver, 356. Sedge, 252.
Soft, 356. Meadow-beauty Family, 371.
Sugar, 360. Meadow-beauty, 371.
Water, 356. Meadow-grass, Annual, 236.
White, 356. Fowl, 236.
Maple-leaved Arrow-wood, 420. Meadow-parsnip, Cut-leaved, 379.
Gocsefoot, 297. Early, 379.
marcellus, Papilio, 38. Hairy-jointed, 379.
marginatus, Pupoides, 75. Meadow-rue, Early, 318.
Marigold, Water, 178, 443. Fall, 314.
marilandica, Cassia, 337. Purplish, 313.
mariscoides, Mariscus, 196, 249. Meadow-sweet, 329.
Mariscus mariscoides, 196, 249. Medeola virginiana, 266.
maritima, Triglochin, 219. media, Alsine, 299.
marmoratus, Hzemopis, 94. medianum, Pisidium, 74.
Lake Maxinkuckee, Physical and Biological Survey
Medic, Black, 339.
Hop, 339.
Medicago lupulina, 339.
Megalodonta beckii, 4438.
Meibomia bracteosa, 342.
canadensis, 3438.
grandiflora, 342.
illinoensis, 343.
marylandica, 345.
michauxii, 342.
nudiflora, 342.
paniculata, 342.
sessilifolia, 342.
melanocarpa, Aronia, 354.
Melanoplus atlanis, 29.
bivittatus, 28, 29.
differentialis, 28, 29.
fasciatus, 29.
femur-rubrum, 28, 29.
Melasoma interrupta, 33, 34.
Melastomacee, 371.
Melilotus alba, 339.
officinalis, 340.
Melosira crenulata, 164.
varians, 164.
Menispermacez, 315.
Menispermum canadense, 315.
Mentha canadensis, 406.
piperita, 406.
spicata, 406.
Menyanthacee, 392.
Menyanthes trifoliata, 392.
meridionalis, Chironomus, 36.
Merismopedia glauca, 142.
Mermaid Family, False, 349.
Mermaid, False, 349.
Mermaid-weed, 374.
Mesadenia atriplicifolia, 446.
tuberosa, 446.
mexicana, Muhlenbergia, 230.
Meyenia leidyi, 104.
Mezereum Family, 370.
Micasterias truncata semiradiata,
153.
michauxiana, Spartina, 235.
michauxii, Meibomia, 342.
Micrampelis lobata, 421.
micrantha, Hemicarpha, 248.
Micranthes pennsylvanica, 323.
microcarpa, Hicoria, 274.
Mercury, Virginia Three-seeded, 351.
microcarpon, Panicum, 226.
Microcystis aeruginosa, 141.
Microgaster, 40.
Micromya fabalis, 72.
microphylla, nymphaea, 305.
microporum, Ceelastrum, 151.
micropteri, Achtheres, 82.
A487
Micropterus salmoides, 14, 18, 80, 82,
100.
dolomieu, 80, 82.
microscopica, Wolffia, 259.
Microthamnion, 155.
Midas’ Ears, 255.
Mild Water Pepper, 295.
miliacea, Zizaniopsis, 228.
militaris, Hibiscus, 366.
milium, Pisidium, 74.
Milk Purslane, 351.
Vetch, Carolina, 341.
Milkweed Family, 395.
Milkweed, 37.
Blunt-leaved, 394.
Butterfly, 37.
Common, 394.
Florida, 396.
Green, 396.
Poke, 394.
Swamp, 394.
alli ao4-
Whorled, 395.
Milkwort Family, 350.
Milkwort, Cross-leaved, 350.
Field, 350.
Marsh, 350.
Purple, 350.
Racemed, 351.
Whorled, 350.
millefolium, Achillea, 444.
Millet, 227.
Mimulus ringens, 410.
minimum, Tetraedron, 150.
minor, Lechea, 368.
Lemna, 167, 258.
Vinea, 392.
Utricularia, 196, 414.
Mint Family, 402.
Mint, American Wild, 406.
minus, Arctium, 446.
minusculus, Zonitoides, 75.
Minute Duckweed, 167, 258.
minutus, Diaptomus, 107.
488
mirabile, Spirogyra, 154.
Mississippi River, 49, 80.
Mississippi sloughs, 63, 78.
Missouri River, 206.
Mitchella repens, 418.
Mitella diphylla, 328.
Mitre-wort, Two-leaved, 323.
Mocker-nut, 274, 275.
moesta putrida, Argia, 20.
Mole Crickets, 29.
mollis, Agrimonia, 331.
Crataegus, 335.
Helianthus, 440.
Mollugo verticillata, 299.
Mollusks, 41.
Mollusks, Fresh-water, 72.
Land, 74.
other than Unionide, 72.
Monarda fistulosa, 404.
punctata, 405.
Moneywort, Prairie, 388.
moniliferum, Pleurocera, 73.
monilis, Ablabesmyia, 36.
Tanypus, 36.
Monkey-flower, Square-stemmed, 410.
monodactyla, Nitella, 160.
monodon, Polygyra, 74.
Monotropacex, 384.
Monotropa uniflora, 384.
monspeliensis, Potentilla, 330.
montifera, Placobdella, 94.
Moonseed Family, 315.
Moonseed, 315.
Moore, Dr. George T., 87, 89, 140,
158.
Moorwort, 386.
Moose-wood, 370.
Moracez, 289.
Morning-glory Family, 396.
Morong, Rev. Thomas, 182.
morsei, Vertigo, 75.
Morus alba, 289.
alba tartarica, 289.
rubra, 289.
Mosely, Prof. H. N., 195.
Mossback, 443.
Mossy-cup Oak, 286.
Motherwort, 404.
Moths, 37.
Mougeotia, 154.
Mt. Etna, Ind., 83.
Lake Maxinkuckee, Physical and Biological Survey
Mountain Holly, 355.
Sumac, 353.
Mountain-mint, 405.
Narrow-leaved, 405.
Mourning’ Cloak, 38.
Mouse-ear Chickweed, Large, 300.
Movements of Mussels, 45.
Mucket, Fat, 65.
mucronata, Nemopanthus, 355.
Nitella, 160.
Mud Lake, 193.
Mud-minnow, 258.
Muhlenbergia, Marsh, 230.
mexicana, 230.
racemosa, 230.
schreberi, 230.
umbrosa, 230.
muhlenbergii, Persicaria, 294.
Quercus, 287.
Mulberry Family, 289.
Mulberry, Red, 289.
Russian, 289.
Mullein-leaved Verbena, 401.
Mullen, Great, 409.
multilineata, Polygyra, 74.
algonquinensis, Polygyra, 74.
multiradiata, Lampsilis, 48, 71.
muscorum, Pupilla, 75.
Musculium rosaceum, 73.
ryckholti, 74.
securis, 74.
transversum, 74.
truncatum, 74.
Musk Turtle, 99.
Musquash Root, 381.
Mussels, Breeding habits and repro-
duction of, 48.
Food and feeding of, 45.
Lakes and ponds as the home of, 41.
Distribution of the lake, 44.
Movements of, 45.
Origin and character of, 42.
Parasites, enemies, and diseases, 49.
Mustard Family, 317.
Mustard, Hedge, 319.
Tall Hedge, 319.
mutata, Eleocharis, 188, 241.
muticum, Cirsium, 447.
mutilum, Hypericum, 367.
Myosotis virginica, 400.
Myricacez, 275.
Lake Maxinkuckee, Physical and Biological Survey 489
myrina, Brenthis, 39.
Myriophyllum heterophyllum, 375.
proserapinacoides, 375.
spicatum, 196, 374, 375.
verticillatum, 175, 375.
Myrtle, Blue, 392.
Myxonema radians, 155.
Nabalus albus, 425.
racemosus, 426.
trifoliolatus, 426.
Naiadaceez, 218.
Naias Family, 218.
Naias flexilis, 184, 218.
flexilis robusta, 173.
Slender, 184, 218.
Stout, 173.
Naked-flowered Tick-trefoil, 342.
nana, Padus, 336.
napus, Brassica, 321.
Narrow Dock, 292.
Narrow-leaved Mountain-mint, 405.
Spleenwort, 203.
nasturtium-aquaticum, Sisymbrium,
188, 318.
natalis, Ameiurus, 79, 80.
natans, Potamogeton, 31, 177, 211,
294.
Rieciocarpus, 168.
Rivularia, 142.
Naumburgia thyrsiflora, 389.
Navicula gastrum, 163.
reinhardtii, 163.
naviculifornis, Cymbella, 163.
nebulosus, Ameiurus, 79, 80.
Necklace Poplar, 278.
Needham, Dr. J. G., 18.
Needle Spike-rush, 189, 242.
Needles, Spanish, 442.
negundo, Acer, 360.
Nebalennia irene, 21.
posita, 22.
Nemopanthus mucronata, 355.
nemoralis, Solidago, 431.
Neoconocephalus robustus, 28, 29.
Nepeta cataria, 402.
nepetoides, Agastache, 402.
nephele, Cercyonis alope, 39.
nervata, Panicularia, 237.
Nerved Manna-grass, 237.
Nettle Family, 290.
Nettle, Canada, 290.
False, 291.
Great, 290.
Hedge, 404.
Slender Wild, 290.
Stinging, 290.
Tall Wild, 290.
Wood, 290.
Nettle-leaved Vervain, 401.
New England Aster, 434.
New Jersey Tea, 362.
New York Fern, 201.
nictitans, Chamaecrista, 337.
Niggerhead, Flat, 51.
Nightshade, Bitter, 408.
Black, 407.
Deadly, 407.
Enchanter’s, 374.
nigra, Betula, 283.
Fraxinus, 390.
Juglans, 272.
Srallibs, Prey
nigrum, Solanum, 407.
Nimblewill, 230.
Ninebark, 329.
Nitella, 182.
batrachosperma, 160.
monodactyla, 160.
mucronata, 160.
tenuissima, 160, 183.
nitida, Crataegus, 335.
nitidus, Zonitoides, 75.
nivicola, Achorutes, 7.
Noble Golden-rod, 430.
nodatus, Juncus, 262.
Nodding Bur-marigold, 441.
Fescue-grass, 238.
Ladies’-tresses, 270, 271.
Sedge, 253.
Wild Onion, 2638.
Wild Rye, 239.
Norta altissima, 319.
Northern Bedstraw, 419.
Comandra, 291.
Fox-grape, 362.
Gooseberry, 326.
Nostoe verrucosum, 148.
Notonectidz, 30.
Notonecta irrorata, 30.
undulata, 30.
novae-angliae, Aster, 434.
490 Lake Maxinkuckee, Physical and Biological Survey
noveboracensis, Dryopterus, 201.
nove-boracensis, Pisidium, 74.
nudicaulis, Aralia, 315, 376.
nudiflora, Meibomia, 342.
numitor, Ancyloxypha, 39.
nutans, Festuca, 238.
Sorghastrum, 224.
Nut-rush, Low, 249.
Nympheacee, 304.
Nymphea advena, 178, 504.
microphylla, 305.
sagittaefolia, 305.
Nyssa sylvatica, 383.
Oak, Bur, 286.
Chestnut, 287.
Chinquapin, 287.
Jerusalem, 297.
Mossy-cup, 286.
Pin, 284.
Push, 286.
Red, 284.
Swamp, 284.
Swamp White, 287.
White, 286.
Yellow, 287.
Yellow-barked, 285.
Oat-grass, Common Wild, 233.
obliqua, Succinea, 75.
obliquum, Botrychium, 197.
obliquus, Scenedesmus, 150.
oblongifolia, Lonicera, 421.
obovatus, Euonymus, 355.
obrussa exigua, Lymnea, 72.
obscura, Gomphoides, 25.
obtusa, Eleocharis, 242.
Synedra, 164.
obtusifolium, Gnaphalium, 437.
obtusifolius, Rumex, 293.
occidentale, Sphzrium, 73.
occidentalis, Celtis, 289.
Cephalanthus, 417.
Helianthus, 439.
Platanus, 327.
Rubus, 331.
octoflora, Festuca, 238.
oculatus, Alaus, 34.
Gelostocoris, 30.
Odonata, Order, 10.
odontorhiza, Corallorrhiza, 271.
odorata, Castalia, 305.
odorata, Savastana, 229.
Oenothera biennis, 372.
Cdogonium boscii, 156.
landsboroughil, 157.
longatum, 157.
officinale, Cynoglossum, 399.
Erysimum, 319.
officinalis, Asparagus, 265.
Melilotus, 340.
Saponaria, 301.
Oleaceex, 389.
oleracea, Portulaca, 299.
oligactis, Hydra, 99.
olivacea, Eleocharis, 242.
olivaceum, Gomphonema, 163.
Olive Family, 389.
Onagracee, 371.
Oncopeltus fasciatus, 31.
Onion, Nodding Wild, 263.
Onoclea sensibilis, 200.
Opercularia irritabilis, 98, 99.
Ophioglossacez, 197.
Ophyrydium, 99.
Opulaster opulifolius, 329.
opulifolius, Opulaster, 329.
Opuntia humifusa, 370.
Orache, Halberd-leaved, 298.
Orange-grass, 367.
Orchard-grass, 236.
Orchidacez, 269.
Orchid Family, 269.
Orchis, Fen, 271.
Green-fringed, 270.
Ragged, 270.
Showy, 269.
Yellow-fringed, 269.
Order, Aptera, 7.
Coleoptera, 33.
Diptera, 35.
Ephemerida, 48.
Hemiptera, 29.
Hymenoptera, 39.
Lepidoptera, 37.
Odonata, 10.
Orthoptera, 27.
Trichoptera, 31.
oregonensis, Diaptomus, 77.
Origin and character of Maxinkuckee
Mussels, 42.
Ornithogalum umbellatum, 264.
Orobanchacee, 415.
Lake Maxinkuckee, Physical and Biological Survey
Orpine Family, 322.
Orthoptera, Order, 27.
oryzoides, Homalocenchrus, 229.
Oscillatoria major, 144.
tenuis, 148.
Osmundacee, 199.
Osmunda cinnamomea, 199.
claytoniana, 200.
regalis, 199.
Ostrya virginiana, 281.
ovalis, Amphora, 163.
ovata, Hicoria, 273.
Ovate-leaved Violet, 369.
Oxalidacez, 348.
Ox-eye, 437.
Ox-eye Daisy, 445.
oxyacanthoides, Grossularia, 326.
Oxycoccus macrocarpus, 387.
Oxypolis rigidus, 379.
Pachydiplax longipennis, 16.
Padus nana, 336.
virginiana, 337.
Paint-brush, Indian, 413.
Painted-cup, Scarlet, 413.
Palaemonetes exilipes, 78.
Pale Persicaria, 294.
Plantain, 446.
Touch-me-not, 349. |
Pale-leaved Wood Sunflower, 440.
pallens, Sphenopholis, 236.
pallida, Impatiens, 349.
pallidus, Lepomis, 80.
palmata, Coreopsis, 440.
Viola, 368.
palustre, Comarum, 330.
palustris, Caltha, 309.
DimcasmrenO:
Eleocharis, 189, 242.
glaucescens, Eleocharis, 189.
Isnardia, 371.
Lathyrus, 344.
Proserpinaca, 374.
Quercus, 284.
Radicula, 317.
Scheuchzeria, 219.
Stachys, 404.
Panax quinquefolium, 376.
trifolium, 377.
pandurata, Ipomoea, 347, 396.
Panic-grass, Barbed, 226.
Panic-Grass, Seribner’s, 226.
Velvety, 227.
Panicled Cornel, 382.
Tick-trefoil, 342.
Panicularia nervata, 237.
septentrionalis, 237.
paniculata, Meibomia, 342.
Panicum ecapillare, 225.
microcarpon, 226.
scoparium, 227.
scribnerianum, 226.
virgatum, 226.
Tall Smooth, 226.
Papaveracee, 317.
Paper-shell, 60.
Papilio glaucus turnus, 38.
marcellus, 38.
polyxenes, 38.
troilus, 38.
papilionacea, Viola, 369.
paradoxa, Cuscuta, 397.
parallelus, Helicodiscus, 75.
Parasites, Copepod, 79.
491
Enemies and diseases of Mussels,
49.
Parasitic Copepods, 77.
parasitica, Placobdella, 92.
parietina, Prasiola, 155.
Parks, Chicago, 324.
Washington, D. C., 324.
Parnassiacez, 323.
Parnassia caroliniana, 323.
Parrot’s Feather, 375.
Parsnip, Hairy-jointed Meadow,
Wild, 378.
Parthenium integrifolium, 437.
Parthenocissus quinquefolia, 365.
Partridge Pea, 338.
Partridge-berry, 418.
parva, Dina, 95.
parviflora, Agrimonia, 331.
Galinsoga, 444.
parvus, Planorbis, 73.
Pastinaca sativa, 378.
Pasture Rose, 333.
patens, Aster, 433.
patula, Solidago, 430.
pauciflora, Strophostyles, 348.
paupercula, Agalinis, 412.
pauperculum, Pisidium, 74.
crystalense, Pisidium, 74.
379.
492 Lake Maxinkuckee, Physical and Biological Survey
pauperculus, Senecio, 446. perennans, Agrostis, 232.
Pawpaw, 306. perennis, Lupinus, 339.
Pea Family, 338. Perethemis domitia, 13.
Pea, Large-flowered Sensitive, 338. perfoliata, Specularia, 422.
Partridge, 338. perfoliatum, Eupatorium, 428.
Sensitive, 337. Triosteum, 421.
Veiny, 344. perfoliatus, Potamogeton, 175, 214.
Pea-nut, Hog, 345. Peridinium tabulatum, 97.
Wild, 345. Periwinkle, 392.
Peach Family, 336. perpusilla, Lemna, 167, 258.
Peach, 337. persica, Amygdalus, 337.
Peach-leaved Dock, 292. Persicaria amphibia, 294.
Willow, 279. hydropiper, 295.
Pear, Western Prickly, 370. hydropiperoides, 295.
pectinatus, Potamogeton, 174, 216. lapathifolia, 294.
pectorale, Gonium, 152. muhlenbergii, 294.
pedata, Viola, 368. pennsylvaniea, 294.
pedatum, Adiantum, 203. persicaria, 294.
Pediastrum boryanum, 151. persicaroides, 295.
duplex, 151. punctata, 295.
ehrenbergii, 151. Dock-leaved, 294.
pedicellaris, Salix, 281. Pale, 294.
pedicularia, Dasystoma, 412. Pennsylvania, 294.
Pedicularis canadensis, 413. Southwestern, 295.
lanceolata, 413. Swamp, 294.
Peltandra virginica, 254. Water, 294.
peltatum, Podophyllum, 315. persicaria, Persicaria, 294.
Pennsylvania Bitter-cress, 320. persicaroides, Persicaria, 295.
Persicaria, 294. persius, Thanaos, 39.
Saxifrage, 323. perspecta, Pyramidula, 75.
Sedge, 251. pestifer, Salsola, 298.
pennsylvanica, Cardamine, 320. Phalaris arundinacea, 229.
Carex, 251. Phalen Lake, Minn., 30.
Fraxinus, 389. Philadelphia Fleabane, 435.
Micranthes, 323. philadelphicus, Erigeron, 435.
Persicaria, 294. philodice, Eurymis, 39.
Photuris, 34. Philotria canadensis, 174, 221.
Pennyroyal, 405. Phleum pratense, 231.
Penthoraceer, 323. Phlox Family, 398.
Penthorum sedoides, 323. divaricata, 398.
Pepin Lake, Minn., 42. pilosa, 398.
Pepper, Mild Water, 295. Downy, 398.
Water, 295. Wild, 398.
Pepper-and-salt, 379. Photuris pennsylvanica, 34.
Pepper-grass, Wild, 318. Phragmites phragmites, 234.
Peppermint, 406. phragmites, Phragmites, 234.
Perca flavescens, 80. Phrymaceex, 416.
percarum, Actheres, 81. Phryma leptostachya, 416.
Perch, Yellow, 80, 100. Phyciodes tharos, 39.
peregrina, Comptonia, 275. Physa heterostropha, 73.
Veronica, 411. integra, 73.
Lake Maxinkuckee, Physical and Biological Survey 493
Physalis lanceolata, 407.
pruinosa, 407.
pubescens, 407.
virginiana, 407.
Phytolaccacex, 298.
Phytolacca americana, 298.
Pickerel-weed Family, 260.
Pickerel-weed, 190, 260.
Pieris floribunda, 386.
protodice, 38, 39.
rape, 37, 39.
Pig-toe, Wabash, 51.
Pigeon-grass, 227.
Pigweed, Slender, 296.
Winged, 297.
Pike, Walleyed, 80, 100.
Pilea pumila, 291.
pilosa, Eragrostis, 235.
Phlox, 398.
pilosum, Galium, 419.
Pimpernel, 410.
Pimpernel, Long-stalked False, 410.
Water, 388.
Yellow, 379.
Pin Oak, 284.
Pin-weed, Thyme-leaved, 368.
Pincushion, 418.
Pinacez, 207.
Pine Family, 207.
Pine, Gray, 207.
Labrador, 207.
Prince’s, 384.
Pine-sap, Hairy, 384.
Pineweed, 367.
Pink Family, 300.
Pink Wild Bean, 348.
pinnata, Porella, 418.
Ratibida, 439.
pinnatifidum, Thaspium, 379.
Pinus banksiana, 207.
Pipe, Indian, 384.
piperita, Mentha, 406.
Pipewort Family, 259.
Pipewort, Seven-angled, 184, 259.
Pipsissewa, 384.
Pisidium abditum, 74.
affine, 74.
compressum, 74.
compressum levigatus, 74.
idahoense, 74.
indianense, 74.
Pisidium lacustrinum, 74.
mainense, 74.
medianum, 74.
milium, 74.
nove-boracense, 74.
pauperculum, 74.
pauperculum crystalense, 74.
politum, 74.
rotundatum, 74.
sargenti, 74.
scutellatum, 74.
splendidulum, 74.
strengu, 74.
subrotundatum, 74.
tenuissimum, 74.
variabile, 74.
vesiculare, 74.
virginicum, 74.
walkeri, 74.
pisiformis, Chetophora, 156.
Pitcher-plant Family, 321.
Pitcher-plant, 321.
Placobdella montifera, 94.
parasitica, 92.
rugosa, 93.
Planarians, 100.
Plane-tree Family, 327.
Plankton, 105.
Plankton, Decrease in, 106.
Distribution of, 106.
Plankton Scum, 110.
Condition of, 112.
Significance of, 112.
Plankton-net, Description of, 105.
Planorbis albus, 73.
bicarinatus, 72.
campanulatus, 73.
exactus, 73.
parvus, 73.
trivolvis, 73.
Plant Lice, 31.
Plant patches in the lake, 134.
Plantaginacee, 416.
plantaginifolia, Antennaria, 456.
Plantago aristata, 417.
lanceolata, 417.
major, 416.
rugelii, 416.
Plantain Family, 416.
Plantain, English, 417.
Large-bracted, 417.
494
Plantain, Pale Indian, 446.
Poor Robin’s, 435.
Rugel’s, 416.
Tuberous Indian, 446.
Plantain-leaf Everlasting, 436.
Platanaceez, 327.
Platanus occidentalis, 327.
Plathemis lydia, 18.
Pleurisy-root, 398.
Pleurocera canaliculatum, 73.
moniliferum, 73.
subulare, 73.
subulare intensum, 73.
undulatum, 73.
Pleuroxus procurvatus, 107.
Plum-grape, 362.
Plum, Wild Red, 336.
Plumatella polymorpha, 102.
Plymouth, Ind., 55, 112, 203, 206, 230,
Paes le, PATO) PAT AL OAT E" Asis PA PAS Te
301, 308, 318, 345, 346, 347, 350,
Stig ASO:
Poa annua, 236.
compressa, 237.
pratensis, 237.
triflora, 236.
Pocketbook, 69.
Podophyllum peltatum, 315.
Poinsettia dentata, 352.
Pointed Blue-eyed Grass, 269.
Pointed-leaved Tick-trefoil, 342.
Poison Ivy, 354.
Sumac, 354.
Poke Milkweed, 394.
Poke-berry, 298.
Poke-root, 298.
Pokegama Lake, Minn., 65, 67, 113.
Pokeweed Family, 298.
Polemoniacez, 398.
Polemonium reptans, 399.
polifolia, Andromeda, 386.
Polita hammonis, 75.
indentata, 75.
politum, Pisidium, 74.
pollutum, Enallagma, 26.
polyecarpa, Ludwigia, 372.
polydermatica, Gloeocapsa, 141.
Polygalacezx, 350.
Polygala cruciata, 350.
polygama, 351.
verticillata, 350.
Lake Maxinkuckee, Physical and Biological Survey
Polygala viridescens, 350.
polygama, Polygala, 351.
polygamum, Thalictrum, 314.
Polygonacee, 292.
Polygonatum biflorum, 266.
commutatum, 266.
Polygonia comma, 38, 39.
interrogationis, 38, 39.
Polygonum aviculare, 261, 293.
erectum, 293.
tenue, 293.
Polygyra elevata, 74.
fraterna, 74.
hirsuta, 74.
monodon, 74.
multilineata, 74.
multilineata algonquinensis, 74.
profunda, 74.
thyroides, 74.
thyroides bucculenta, 74.
zaleta, 74.
polymorpha, Plumatella, 102.
Polypodiaceez, 200.
polyrhiza, Spirodela, 166, 256.
Polystichum acrostichoides, 200.
polyxenes, Papilio, 38.
Pomoxis sparoides, 80.
Pond Crawfish, 84.
Lily, 180.
Lily, Large Yellow, 178, 304.
Pondweed Family, 211.
Pondweed, Clasping-leaved, 175, 214.
Common Floating, 177, 211.
Eel-grass, 169, 215.
Fennel-leaved, 216.
Filiform, 170.
Fries’, 169, 215.
Interrupted, 178.
Large-leaved, 171, 213.
River, 176, 218.
Robbins’, 170, 217.
Shining, 176, 214.
Small, 170, 215.
Various-leaved, 177, 213. :
White-stemmed, 214.
Pontederiacez, 260.
Pontederia cordata, 190, 260.
Poor Robin’s Plantain, 435.
Popcorn, Devil’s, 415.
Poplar, Downy, 276.
Necklace, 278.
Lake Maxinkuckee, Physical and Biological Survey
Poplar, Silver-leaf, 275.
Swamp, 276.
White, 275.
Yellow, 305.
Poppy Family, 317.
Populus alba, 275.
candicans, 275.
deltoides, 278.
grandidentata, 376.
heterophylla, 276.
tremuloides, 276.
porata, Amnicola limosa, 73.
Porcellio scaber, 78. .
Porcupine-grass, 229.
Porella pinnata, 418.
Portulacacee, 299.
Portulaca oleracea, 299.
posita, Nehalennia, 22.
Potamogeton americanus, 176, 213.
amplifolius, 171, 212.
compressus, 169, 215.
filiformis, 170, 216.
friesii, 169, 215.
heterophyllus, 177, 213.
interruptus, 178.
lucens, 176, 214.
natans- ol, 177, 20) 294.
pectinatus, 174, 216.
perfoliatus, 175, 214.
praelongus, 214.
pusillus, 170, 215.
robbinsii, 170, 217.
Potamogetons, 312.
Potato Family, 407.
Potato, Sweet, 347.
Wild, 344.
Vine, Wild, 396.
Potentilla canadensis, 330.
monspeliensis, 330.
Potter-wasp, 40.
Potts, Edward, 108.
Poverty-grass, 230.
praelongus, Potamogeton, 214.
Prairie Burdock, 487.
Button-snakeroot, 429.
Dock, 437.
Chloris, 233.
Ground-cherry, 407.
Moneywort, 388.
Wake-robin, 267.
prasinus, Cyclops, 107.
Prasiola parietina, 155.
pratense, Phleum, 2351.
Poa, 237.
Trifolium, 340.
preslii, Chamaesyce, 351.
Pretty Lake, 42, 56, 65.
Prickly Ash, 350.
Lettuce, 424.
Pear, Western, 370.
Sida, 365.
Primrose Family, 388.
Primulacee, 388.
princeps, Epicordulia, 25.
Prince’s Pine, 384.
procumbens, Gaultheria, 387.
Rubus, 3382.
Procumbent Wood-sorrel, Yellow, 349.
procurvatus, Pleuroxus, 107.
profunda, Polygyra, 74.
promethea, Callosamia, 39.
propinquus, Cambarus, 83, 85.
Proserpinaca palustris, 374.
proserpinacoides, Floerkea, 349.
Myriophyllum, 375.
prostrata, Cymbella, 164.
Prostrate Amaranth, 296.
Tick-trefoil, 342.
protodice, Pieris, 38, 39.
Protozoans, 95.
pruinosa, Physalis, 407.
Prunella vulgaris, 403.
prunifolium, Viburnum, 420.
Prunus americana, 336.
Psephenus lecontei, 33, 34.
pseudargiolus, Lycnopsis, 39.
pseudo-acacia, Robinia, 341.
psilostachya, Ambrosia, 427.
Psorophora ciliata, 36.
Ptelea trifoliata, 31, 350.
Pteridium aquilinum, 203.
Pterophylla camellifolia, 28, 29.
pubescens, Physalis, 407.
Viola, 370.
Puccoon, Hairy, 400.
Hoary, 400.
Puccoon-root, 317.
pulchella, Vallonia, 75.
Goniobasis, 73.
Libellula, 11, 16, 26.
pulchellus, Erigeron, 435.
pulegioides, Hedeoma, 405.
496 Lake Maxinkuckee, Physical and Biological Survey
pulex pulicaria, Daphnia, 107.
pulicaria, Daphnia, 107.
pumila, Betula, 283.
Kyllinga, 239.
Kneiffia, 373.
Pilea, 291.
punctata, Erpobdella, 94.
Monarda, 405.
Persicaria, 295.
Wolffia, 259.
punctatum, Hypericum, 366.
punctatus, Ictalurus, 80.
puniceus, Aster, 434.
Pupoides marginatus, 75.
Pupilla muscorum, 75.
Purple Aster, 434.
Aster, Late, 4338.
Bladderwort, 192, 413.
Cinquefoil, 330.
Cone-flower, 439.
Cress, 320.
Milkwort, 350.
Purple-leaved Willow-herb, 372.
Purple-stem Aster, 434.
Purple-stemmed Angelica, 379.
Beggar-Ticks, 441.
Purplish Meadow-Rue, 313.
Wheat-grass, 238.
purpurascens, Aristida, 230.
purpurea, Echinacea, 439.
Sarracenia, 321.
Vesiculina, 192, 413.
purpureum, Eupatorium, 428.
purshii, Eragrostis, 235.
Ranunculus, 312.
Pursh’s Buttercup, 312.
Love-grass, 235.
Purslane Family, 299.
Purslane, Marsh, 371.
Milk, 351.
Speedwell, 411.
Push Oak, 286.
pusillus, Potamogeton, 170, 215.
Pussy Willows, 280.
Put-in-Bay, 54, 258, 422.
putrida, Argia moesta, 20.
Putty-root, 271.
pycnocarpon, Asplenium, 203.
pycnostachya, Lacinaria, 429.
pygmea, Bulbochete, 156.
pylades, Cocceius, 39.
Pyramidula alternata, 74.
cronkhitei anthonyi, 74.
perspectiva, 75.
Pyrgus tessellata, 39.
Pyrolaceex, 384.
Pyrola elliptica, 384.
quadrangulata, Fraxinus, 390.
quadratum, Desmidium, 152.
quadriflorum, Steironema, 388.
quadrifolia, Lysimachia, 388.
quadrimaculata, Anopheles, 36.
Libellula, 17.
quadripartata, Tokophyra, 99.
Quadrula coccinea, 44, 51.
undulata, 44.
rubiginosa, 44, 51.
rubiginosa, Food of, 52.
Quaking Asp, 276.
Queen Anne’s Lace, 381.
Quercitron, 285.
Quercus alba, 286.
bicolor, 287.
coccinea, 285.
macrocarpa, 286.
muhlenbergii, 287.
palustris, 284.
rubra, 284.
velutina, 285.
Quick Will, 255.
quinquefolia, Anemone, 310.
Gentiana, 391.
Parthenocissus, 363.
quinquefolium, Panax, 376.
Rabbit Tobacco, 444.
Rabbit-foot Clover, 340.
Racemed Milkwort, 351.
racemosa, Aralia, 376.
Vagnera, 265.
racemosus, Nabalus, 426.
radians, Myxonema, 155.
Synedra, 164.
radicans, Bignonia, 416.
Toxicodendron, 354.
Radicula palustris, 317.
radula, Solidago, 432.
Ragged Orchis, 270.
Ragweed Family, 426.
Ragweed, 426.
Lake Maxinkuckee, Physical and Biological Survey
Ragweed, Great, 426.
Western, 427.
Rainbow-shell, 61.
ramosus, Erigeron, 436.
Ranatra fusca, 30.
Ranunculaceex, 308.
Ranunculus, abortivus, 312.
bulbosus, 313.
delphinifolius, 311.
hispidus, 313.
purshii, 312.
recurvatus, 312.
rape, Pieris, 37.
Rape, 321.
Raspberry, Black, 331.
Dwarf Red, 332.
Wild Red, 331.
Ratibida pinnata, 439.
Rattle-box, 372.
Rattlesnake-fern, 198.
Rattlesnake-master, 377.
Rattlesnake-root, Tall, 426.
Reclined Bladderwort, 192, 415.
recurvatum, Trillium, 267.
recurvatus, Ranunculus, 312.
Red Admiral, 38.
Ash, 389.
Birch, 283.
Cedar, 209.
Choke-berry, 334.
Clover, 340.
Elm, 288.
Haw, 385.
Lily, Western, 263.
Maple, 359.
Mulberry, 289.
Oak, 284.
Plum, Wild, 336.
Raspberry, Dwarf, 332.
Raspberry, Wild, 331.
Sorrel, 292.
Wood-lettuce, 425.
Red-bud, 337.
Red-fruited Thorn, 335.
Red-osier Dogwood, 382.
Red-root, 362.
Red-stalk Aster, 434.
Red-top, 232.
Red-top, False, 236.
Reddish Bulrush, 248.
Redeye, 11, 80, 81.
32—17618—Vol. 2
Reed Canary-grass, 229.
Reed-grass, Bog, 233.
Common, 234.
Wood, 231.
reflexa, Tradescantia, 260.
Reflexed Spiderwort, 260.
regalis, Osmunda, 199.
regine, Cypripedium, 269.
reinhardtii, Navicula, 163.
remigis, Gerris, 30.
Hygrotrechus, 30.
repens, Epigaea, 386.
Mitchella, 418.
Trifolium, 341.
reptans, Polemonium, 399.
resupinata, Leticula, 192.
reticulata, Chlamydomonas, 152.
reticulatum, Hydrodictyon, 151.
retrocurva, Daphina, 77, 107.
retroflexus, Amaranthus, 296.
retusa, Succinea, 75.
Rhamnaceez, 362.
Rhexia virginica, 371.
Rhoicosphenia curvata, 163.
rhomboideum, Sphaerium, 73.
Rhubarb, Wild, 292.
Rhus arbuscula, 353.
copallina, 353.
glabra, 353.
hirta, 353.
Ribbed Sedge, 252.
Ribes americanum, 326.
Ribwort, 417.
Riccia, 168, 312.
Riccia lutescens, 380.
Ricciocarpus natans, 168.
Rice Cut-grass, 229.
Rice, Wild, 228.
Richweed, 291.
Ridan alternifolius, 440.
riddellii, Solidago, 432.
Riddell’s Golden-rod, 432.
rigida, Solidago, 432.
ringens, Mimulus, 410.
River, Chester, 78.
Cumberland, 361.
497
Kankakee, 42, 51, 56, 78, 285, 366.
Maumee, 49, 62, 78, 361.
Mississippi, 49, 80.
Missouri, 206.
St. Mary’s, 298.
498
Tippecanoe, 15, 16, 19, 21, 43, 44,
pi ba, 55,206, 61,62, 715: 72, S00,
308, 314, 349, 356, 366.
Wabash, 43, 63.
Yellow, 15, 16, 18, 19, 42, 49, 51, 55,
56, 71, 272, 282, 283, 306, 308,
314,
Birch, 2838.
Pondweed, 176, 2138.
River-bank Willow, 279.
Riverside Grape, 363.
Rivularia dura, 1438.
echinula, 142.
haematiles, 148.
natans, 142.
rivularis, Ancylus, 73.
Roadside Thistle, 447.
Robbins’ Pondweed, 170, 217.
robbinsii, Potamogeton, 170, 217.
Robinia pseudo-acacia, 341.
Robinson, Prof. C. B., 140, 158, 159,
160, 182.
robusta, Chamaecrista fasciculata,
338.
Naias flexilis, 173.
robustum, Equisetum, 205.
robustus, Neoconocephalus, 28, 29.
Rochester, Ind., 275.
Rock Crawfish, 86.
Creek, 285.
Rock-cress, Hairy, 319.
Smooth, 319.
Rock-rose Family, 367.
Root, Musquash, 381.
Rosacez, 329.
Rose Family, 329.
Rosa carolina, 333.
rubiginosa, 333.
virginiana, 333.
rosaceum, Musculium, 73.
Rose, Low, 333.
Marsh Holy, 386.
Pasture, 333.
Swamp, 333.
Wild, 3383.
Rose-mallow, Halberd-leaved, 366.
Rose-pink, 390.
rosea, Carex, 249.
Rosemary, Wild, 386.
Rosin-wood, Entire-leaved, 437.
rostrata, Carex, 253.
Lake Maxinkuckee, Physical and Biological Survey
rostrata, Viola, 370.
rotundatum, Pisidium, 74.
rotundifolia, Campanula, 422.
Drosera, 321.
Malva, 364.
Smilax, 267.
Rough Cinquefoil, 330.
Golden-rod, Western, 4382.
Hair-grass, 232.
Heuchera, 323.
Sunflower, 440.
Rough-leaved Golden-rod, 430.
Round-headed Bush-clover, 343.
Round-leaved Sundew, 321.
Tick-trefoil, 342.
Round-lobed Liver-leaf, 310.
Liverwort, 310.
Round-podded St. John’s-wort, 366.
Round-worms, 100.
Royal Fern Family, 199.
Royal Fern, 199.
Rubiacex, 417.
rubicundulum, Sympetrum, 26.
rubiginosa, Quadrula, 44, 51.
Rosa, 333.
rubra, Morus, 289.
Quercus, 284.
rubrum, Acer, 359.
Rubus argutus, 332.
hispidus, 333.
occidentalis, 331.
procumbens, 3382.
strigosus, 3381.
triflorus, 3382.
Rudbeckia hirta, 438.
laciniata, 438.
Rue Family, 350.
Rue Anemone, False, 309.
Goat’s, 341.
Rue-anemone, 311.
rugelii, Plantago, 416.
Rugel’s Plantain, 416.
rugosa, Placobdella, 95.
Solidago, 430.
Rumex acetosella, 292.
altissimus, 292.
crispus, 292, 293.
obtusifolius, 293.
Running Blackberry, Low, 332.
Strawberry Bush, 355.
Swamp Blackberry, 333.
Lake Maxinkuckee, Physical and Biological Survey 499
rupestris, Ambloplites, 80.
Rush Aster, 434.
Rush Family, 261.
Rush, Bog, 261.
Canada, 262.
Chair-maker’s, 245.
Common, 261.
Sharp-fruited, 262.
Slender, 261.
Soft, 261.
Stout, 262.
Toad, 261.
Twig, 196.
pYsciEd 5 Ail
Rush-grass, Long-leaved, 231.
Sheathed, 2381.
Rushy Golden-rod, 432.
Russian Mulberry, 289.
Thistle, 298.
rusticus, Cambarus, 83.
Rutaceex, 350.
ryckholti, Musculium, 74.
Rynchospora alba, 249.
Sabbatia angularis, 390.
saccata, Anabena, 148.
saccharinum, Acer, 356.
saccharum, Acer, 360.
Sage Willow, 281.
Wood, 402.
sagittaefolia, Nymphza, 305.
Sagittaria graminea, 184, 220, 259.
latifolia, 219.
Grass-leaved, 220.
sagittatum, Tracaulon, 295.
St. John’s-wort Family, 366.
St. John’s-wort, Copper-colored, 366.
Dwarf, 367.
Marsh, 367.
Round-podded, 366.
Spotted, 366.
Virgate, 366.
St. Mary’s River, 298.
St. Paul, Minn., 96, 245.
Salicaceze, 275.
Salix alba, 279.
amyegdaloides, 279.
bebbiana, 280.
cordata, 280.
discolor, 280.
Salix interior, 279.
lucida, 279.
nigra, 278.
pedicellaris, 281.
sericea, 280.
tristis, 281.
salmoides, Micropterus, 14, 18, 80, 82,
100.
salmonia, Anodonta, 60.
Salsola pestifer, 298.
Salt Marsh Cockspur-grass, 225.
Sambucus canadensis, 420.
Samolus floribundis, 388.
Sandalwood Family, 291.
Sandbar Willow, 279.
Sandwort, Thyme-leaved, 300.
sanguinale, Syntherisma, 224.
Sanguinaria canadensis, 317.
Sanicle, 377.
Sanicula marylandica, 377.
Santalacez, 291.
saponaria, Dastystephana, 391.
Saponaria officinalis, 301.
sargenti, Pisidium, 74.
Sarothra gentianoides, 367.
Sarracenia purpurea, 321.
Sarracenicacez, 321.
Sarsaparilla, Wild, 315.
Wild Virginian, 376.
Sassafras, 315.
Sassafras sassafras, 315.
sassafras, Sassafras, 315.
Satin-grass, 230.
sativa, Camelina, 317.
Cannabis, 290.
Pastinaca, 378.
Satyrodes canthus, 39.
Saururacez, 272.
Saururus cernuus, 272.
Savastana odorata, 229.
Saxifragacezx, 323.
Saxifrage Family, 323.
Saxifrage, Pennsylvania, 323.
Swamp, 323.
Say, Thomas, 94.
scaber, Porcellio, 78.
Scabious, Sweet, 435.
Scale Insects, 29.
scandens, Celastrus, 355.
scariosa, Lacinaria, 429.
Searlet Painted-cup, 413.
500
Searlet Sumac, 353.
Thorn, 335.
Scenedesmus abundans, 150.
obliquus, 150.
Scented, Grape Sweet, 363.
Scepsis fulvicollis, 39.
Scheuchzeriaceez, 219.
Scheuchzeria palustris, 219.
Schizachyrium scoparium, 223.
Schizomeris liebleinii, 156.
schreberi, Brasenia, 303.
Muhlenbergia, 230.
schwartzii, Desmidium, 152.
schribnerianum, Panicum, 226.
Seribner’s Panic-grass, 226.
Scirpus americanus, 186, 245.
cyperinus, 248.
debilis, 196, 245.
lineatus, 248.
subterminalis, 245.
validus, 185, 246.
Seleria verticillata, 249.
scoparia, Kochia, 297.
scoparium, Panicum, 227.
Schizachyrium, 223.
Scorpion, Water, 30.
Scorpion-grass, Spring, 400.
Scouring-rush, Smooth, 206.
Stout, 205.
Sonal, ID)ies dg kG ilival, PAS SPAS Bie).
392, 396, 419, 437.
Scrophulariacez, 409.
Scrophularia leporella, 409.
marylandica, 409.
Scudderia curvicauda, 29.
Seull, Dr, 275.
Seum, Plankton, 110.
scutata, Coleochoete, 156.
Scutellaria galericulata, 402.
lateriflora, 402.
scutellata, Veronica, 411.
scutellatum, Pisidium, 74.
Seal, Golden, 308.
Seaside Arrow-grass, 219.
secalinus, Bromus, 238.
securis, Musculium, 74.
Sedge Family, 239.
Sedge, Awl-fruited, 250.
Awned, 253.
Beaked, 253.
Bebb’s, 250.
Lake Maxinkuckee, Physical and Biological Survey
Sedge, Blunt Broom, 250.
Bristle-stalked, 251.
Bristly, 190, 253.
Broad-winged, 250.
Brown, 252.
Fox, 249.
Graceful, 252.
Gray, 252.
Hay, 251.
Hirsute, 252.
Hop, 253.
Large Panicled, 250.
Lesser Panicled, 250.
Meadow, 252.
Nodding, 253.
Pennsylvania, 251.
Ribbed, 252.
Stellate, 249.
Straw, 250.
Tussock, 252.
White Bear, 251.
Woolly, 258.
sedula, Argia, 21.
Sedum triphyllum, 322.
sedoides, Penthorum, 323.
Seed-box, 372.
Segmentina armigera, 73.
Selaginellacew, 207.
Selaginella Family, 207.
Selaginella apus, 207.
Creeping, 207.
Self-heal, 403.
semiradiata,
153.
Senecio pauperculus, 446.
Senna Family, 337.
Senna, American, 337.
Wild, 387.
sensibilis, Onoclea, 200.
Sensitive Fern, 200.
Pea, 337.
Pea, Large-flowered, 338.
sepium, Convolvulus, 397.
Miseasterias
truncata,
septangulare, Eriocaulon, 184, 259.
septentrionalis, Panicularia, 237.
sericea, Salix, 280.
serotina, Solidago, 4381.
serpentaria, Aristolochia, 292.
serpyllifolia, Arenaria, 300.
Veronica, 411.
serratus, Branchipus, 77.
Lake Maxinkuckee, Physical and Biological Survey 501
Service-berry, 335.
Sessile-leaved Tick-trefoil, 342.
sessilifolia, Meibomia, 342.
Seven-angled Pipewort, 184, 259.
Sewickley, Pa., 128, 349, 444.
Shag-bark, 273, 275.
Sharp-fruited Rush, 262.
Sharp-lobed Liverwort, 311.
Sharp-toothed Golden-rod, 431.
Sheathed Rush-grass, 231.
Sheep-berry, 420.
Sheep-sorrel, 348.
Shell-bark Hickory, 273.
Shepherd’s-purse, 317.
Shield-fern, Crested, 201.
Marsh, 201.
Spinulose, 202.
shimekii, Ancylus, 73.
Shin-leaf, 384.
Shining Bedstraw, 420.
Pondweed, 214.
Thorn, 335.
Willow, 279.
Shoestrings, 341.
Shooting Star, 389.
Short-fruited Rush, 262.
Showy Goldren-rod, 430.
Ladies’-slipper, 269.
Orchis, 269.
Tick-trefoil, 343.
Shrews, 100.
Shrimp, Freshwater, 78.
Shrubby Bittersweet, 355.
sicculus, Labidesthes, 100.
Sickle-pod, 319.
Sida erystallina, 107.
spinosa, 365.
Prickly, 365.
signatum, Enallagma, 23.
Silene antirrhina, 301.
latifolia, 300.
stellata, 300.
Silkweed, 394.
Silky Cornel, 382.
Willow, 280.
Silphium integrifolium, 437.
terebinthinaceum, 437.
Silver Maple, 356.
Silver-leaf Poplar, 275.
Silvery Spleenwort, 203.
Simaroubaceex, 350.
simile, Spherium, 73.
Simms, E. G., 194.
Simple-stemmed Bur-reed, 211.
simplex, Sparganium, 211.
Valvata sincera, 73.
simplicicollis, Erythemis, 15.
Simpson, Chas. T., 63.
Sinapis arvensis, 321.
sincera, simplex, Valvata, 73.
Sisymbrium nasturtium-aquaticum,
188, 318.
Sisyrinchium angustifolium, 269.
Sium cicutaefolium, 380.
Skipjack, 100.
Skulleap, Mad-dog, 402.
Marsh, 402.
Speedwell, 411.
Skunk Cabbage, 255.
Sky-blue Aster, 433.
Sleepy Catchfly, 301.
Slender Bush-clover, 343.
Cotton-grass, 243.
Crab-grass, 224.
Cyperus, 241.
Fescue-grass, 288. ©
Fimbristylis, 243.
Finger-grass, 224.
Forked Chickweed, 298.
Fragrant Golden-rod, 482.
Knotweed, 293.
Naias, 184, 218.
Nettle, 290.
Pigweed, 296.
Rush, 261.
Wild Nettle, 290.
Yellow-eyed Grass, 259.
Slippery Elm, 288.
Sloughs of the Mississippi, 78.
Small Bedstraw, 419.
Bur-grass, 227.
Coral-root, 271.
Pondweed, 170, 215.
Sundrops, 373.
Tufted Love-grass, 254.
White Aster, 4384.
Wild Bean, 348.
Small-flowered Agalinis, 412.
Small-fruited Hickory, 254, 274.
Small-leaved Tick-trefoil, Smooth,
343.
Small-mouthed Black Bass, 80.
502 Lake Maxinkuckee, Physical and Biological Survey
Smaller Bur-marigold, 441.
Smart-weed, Dotted, 295.
Water, 295.
Smilacez, 267.
Smilax Family, 267.
Smilax herbacea, 267.
hispida, 268.
rotundifolia, 267.
Smooth Aster, 434.
Bur-marigold, 441.
Creeping Love-grass, 236.
False Foxglove, 412.
Rock-cress, 219.
Scouring-rush, 206.
Small-leaved Tick-trefoil, 348.
Solomon’s Seal, 266.
Upland Sumac, 353.
Smoother Sweet-cicely, 378.
Snake-feeder, 10.
Snake-head, 410.
Snakeroot, Black, 377.
Button, 377.
Virginia, 292.
White, 292.
Snap Dragon, Wild, 410.
Snapping Turtle, 4438.
Snipe, Wilson, 88.
Snout Beetles, 34.
Snow-drops, 310.
Snowfleas, 7.
Soapwort, 301.
Soapwort Gentian, 391.
Soft Agrimony, 331.
Fox Sedge, 249.
Maple, 356.
Rush, 261. |
Solanacez, 407.
Solanum carolinense, 408.
duleamara, 408.
nigrum, 407.
solea, Cymatopleura, 163.
Solidago caesia, 429.
canadensis, 431.
flexicaulis, 429.
hispida, 430.
juncea, 431.
nemoralis, 431.
patula, 430.
radula, 432.
riddellii, 432.
rigida, 432.
Solidago rugosa, 430.
serotina, 431.
speciosa, 430.
uliginosa, 430.
ulmifolia, 430.
solidum, Spherium, 73.
Solitary Crawfish, 84.
Solomon’s Seal, Hairy, 266.
Smooth, 266.
Star-flowered, 265.
Sonchus asper, 424.
Sorastrum, 150.
Sorghastrum nutans, 224.
Sorrel, Field, 292.
Red, 292.
Sour Gum, 383.
Southern Cabbage Butterfly, 38.
Wood Violet, 369.
Yellow Birch, 283.
Southwestern Persicaria, 295.
Sowbugs, 79.
Sow-thistle, Spiny, 424.
Spanish Needles, 442.
Sparganium simplex, 211.
sparoides, Pomoxis, 80.
Sparrow, English, 317.
spartea, Stipa, 229.
Spartina michauxiana, 233.
Spathyema foetida, 255.
Spatulate-leaved Sundew, 322.
Spear-grass, Low, 236.
Spearmint, 406.
speciosa, Catalpa, 416.
Solidago, 430.
Specularia perfoliata, 422.
Speedwell, Corn, 411.
Marsh, 411.
Purslane, 411.
Skulleap, 411.
Thyme-leaved, 411.
Water, 410.
sphericum, Ceelastrum, 151.
Spherium flavum, 73.
occidentale, 73.
rhomboideum, 73.
simile, 73.
solidum, 73.
stamineum, 73.
striatinum, 73.
suleatum, 73.
tenuis, 73.
Lake Maxinkuckee, Physical and Biological Survey
Spherium tumidulum, 73.
walkeri, 738.
Sphenopholis pallens, 236.
spicata, Danthonia, 253.
Lacinaria, 429.
Lactuca, 425.
Mentha, 406.
spicatum, Myriophyllum, 196, 374, 875.
Spice-bush, 316.
Spicy Wintergreen, 387.
Spiderwort Family, 260.
Spiderwort, Reflexed, 260.
Spike, 53.
Spike-rush, Angled, 188, 241.
Blunt, 242.
Bright Green, 242.
Creeping, 189, 242.
Knotted, 188, 241.
Needle, 189, 242.
Spiked Lobelia, 423.
Water-milfoil, 196, 374.
Spikenard, American, 376.
False, 265.
spinifer, Ilyocryptus, 107.
spinirostris, Cambarus immunis, 86.
spinosa, Sida, 365.
spinulosa, Dryopteris, 202.
Spinulose, Shield-fern, 202.
Spiny Sow-thistle, 424.
Spiraea alba, 329.
tomentosa, 330.
spiralis, Vallisneria, 171, 222.
Spirodela polyrhiza, 166, 256.
Spirogyra condensata, 155.
majuscula, 154.
mirabile, 154.
Spirulina jenneri, 143, 148.
spithamaeus, Convolvulus, 397.
Spleen Amaranth, 296.
Spleenwort, Narrow-leaved, 203.
Silvery, 203.
splendidulum, Pisidium, 74.
Sponges, 103.
Sporobolus asper, 231.
vaginaeflorus, 231.
Spotted St. John’s-wort, 366.
Spurge, 351.
Spurge, Upright, 351.
Touch-me-not, 349.
Spreading Dogbane, 392.
Spreading Spurge, Hairy, 351.
Spring Beauty, 299.
Cress, 320.
Harbinger of, 279.
Scorpion-grass, 400.
Spring-tails, 7.
Spurge Family, 351.
Spurge, Blooming, 352.
Blotched, 351.
Cypress, 352.
Flowering, 352.
Hairy Spreading, 351.
Large Spotted, 351.
Spotted, 351.
Toothed, 352.
Upright Spotted, 351.
Square-stemmed Monkey-flower, 410.
Squawfoot, 60.
Squaw-root, 415.
Squirrel-tail Grass, 288.
Stachys palustris, 404.
Staff-tree Family, 355.
Stag-beetles, 34.
Staghorn Sumac, 355.
stagnalis, Anabzna, 148.
Glossiphonia, 90.
stagnina, Aphanotheca, 142.
stamineum, Spherium, 73.
Staphyleacez, 356.
Staphylea trifolia, 356.
Star, Shooting, 389.
Star-of-Bethlehem, 264.
Star-flower, 389.
Star-flowered Solomon’s Seal, 265.
Star-grass, 164.
Water, 261.
Yellow, 268.
Starry Campion, 300.
Staurastrum brebissonii, 152.
Steeple-bush, 330.
Steironema ciliatum, 388.
quadrilorum, 388.
stellata, Silene, 300.
Vagnera, 265.
Stellate Sedge, 249.
Stenelmis sulcatus, 34, 46.
Stenophyllus capillaris, 243.
Stentor coeruleus, 97.
Stevenson, Robert Louis, 235.
Stick-tight, 442.
Stickleback, 76.
Stiff Gentian, 391.
504. Lake Maxinkuckee, Physical and Biological Survey
Stiff Golden-rod, 482.
Marsh Bed-straw, 419.
Tickseed, 440.
White Water Crow-foot, 187.
Stiff-haired Sunflower, 440.
Stiff-leaved Aster, 436.
stimulans, Culex, 36.
Stinging Nettle, 290.
Stipa spartea, 229.
stipata, Carex, 250.
Stitchwort, Long-leaved, 300.
Stizostedion vitreum, 80.
stolonifera, Cornus, 382.
Stonecrop, Ditch, 323.
Stout Naias, 178.
Rush, 262.
Scouring-rush, 205.
straminea, Carex, 250.
stramonium, Datura, 408.
Straw Bass, 100.
Sedge, 250.
Straw-colored Cyperus, 240.
Strawberry Bush, Running, 355.
Virginia, 330.
Wild, 3380.
strengii, Pisidium, 74.
striata, Lespedeza, 343.
striatinum, Spherium, 73.
stricta, Carex, 252.
Verbena, 401.
Xanthroxalis, 348.
strigosus, Cyperus, 240.
Rubus, 331.
Strobilops affinis, 75.
labyrinthica, 75.
virgo, 75.
Strong-scented Love-grass, 234.
Strophitus edentulus, 60.
Strophostyles helvola, 346.
pauciflora, 348.
umbellata, 348.
strumosus, Helianthus, 440.
styraciflua, Liquidambar, 325.
subcordatum, Alisma, 219.
subcrenatum, Cosmarium, 153.
subrostrata, Lampsilis, 44, 63.
subrotundatum, Pisidium, 74.
subterminalis, Scirpus, 245.
subulare, Pleurocera, 73.
intensum, Pleurocera, 73.
subverrucosa, Chara, 160.
Succinea avara, 75.
obliqua, 75.
retusa, 75.
Sucker, Carp, 258.
Sugar Maple, 360.
Sugar-berry, 289.
Sugar-tree, 360.
suleatum, Spherium, 73.
suleatus, Stenelmis, 34, 46.
Sumac Family, 353.
Sumac, Dwarf Black, 353.
Greene’s, 353.
Mountain, 353.
Scarlet, 353.
Smooth Upland, 353.
Staghorn, 353.
Swamp, 354.
Summer Grape, 362.
Sundew Family, 321.
Sundew, Round-leaved, 321.
Spatulate-leaved, 322.
Sundrops, Small, 373.
Sunflower, Common, 439.
False, 437.
Few-leaved, 439.
Giant, 439.
Hairy, 440.
Pale-leaved Wood, 440.
Rough, 440.
Stiff-haired, 440.
Tall, 439.
Wild Giant, 439.
Woodland, 440.
superbum, Lilium, 263, 264.
Susan, Black-eyed, 438.
Swallowtail, Ajax, 38.
Zebra, 38.
Swamp Beggar-ticks, Purple-stem-
med, 441.
Blackberry, Running, 333.
Fly-honeysuckle, 421.
Hickory, 272.
Horsetail, 205.
Lousewort, 413.
Loosestrife, 191, 370.
Milkweed, 394.
Oak, 284.
Persicaria, 294.
Poplar, 276.
Rose, 333.
Saxifrage, 323.
Lake Maxinkuckee, Physical and Biological Survey
Swamp Sumac, 354.
Thistle, 447.
White Oak, 287.
Willow, 278.
Sweet Balsam, 437.
Fern, 275.
Flag, 256.
Gum, 325.
Potato, 347.
Seabious, 435.
Scented Grape, 363.
White Violet, 369.
Sweet-cicely, Hairy, 377.
Smoother, 378.
Wooly, 377.
Sweet-clover, Yellow, 340.
White, 339.
Sweet-scented White Water Lily, 305.
Sweetbrier, 333.
Swimmers, Black, 30.
Sycamore, 327.
sylvatica, Nyssa, 383.
Sympetrum corruptum, 15.
rubicundulum, 26.
vicinum, 15.
Symphynota compressa, 44.
costata, 44.
Syndesmon thalictroides, 311.
Synedra longissima, 164.
obtusa, 164.
radians, 164.
Syntherisma ‘filiforme, 224.
sanguinale, 224.
syphilitica, Lobelia, 423.
syriaca, Asclepias, 39, 394.
tabulatum, Peridinium, 97.
Taenidia integerrima, 379.
Tajo, Yerba de, 438.
Tall Anemone, 310.
Bellflower, 422.
Blackberry, 332.
Blue Lettuce, 425.
Cone-flower, 438.
Cotton-grass, 244,
Mock w292-
Eaton’s-grass, 236.
Grama-grass, 2353.
Hairy Ground-cherry, 407.
Hedge Mustard, 319.
Iron-weed, 427.
Tall Marsh-grass, 233.
Milkweed, 394.
Rattlesnake-root, 426.
Smooth Panicum, 226.
Sunflower, 439.
Thistle, 447.
Tickseed, 440.
Tickseed-sunflower, 442.
White Aster, 436.
Wild Nettle, 290.
Wormwood, 445.
Tamarack, 208.
Tanaceum vulgare, 445.
Tansy, 445.
Tanypus monilis, 36.
Tanytarsus dives, 36.
Tape-grass Family, 221.
Tape-grass, 171, 222.
Tapeworms, 100.
tappaniana, Gastrocopta, 75.
tardus, Ancylus, 73.
taraxacum, Leontodon, 424.
tartarica, Cornus, 382.
Morus alba, 289.
Tea, New Jersey, 362.
Tear-thumb, Arrow-leaved, 295.
Halberd-leaved, 296.
tenue, Polygonum, 293.
tenuifolia, Euthamia, 432.
tenuis, Juncus, 261.
Oscillatoria, 143.
Spherium, 73.
Tolypothrix, 148.
tenuissima, Nitella, 160, 185.
Ulothrix, 156.
tenuissimum, Pisidium, 74.
terebinthinaceum, Silphium, 437.
Ternate Grape-fern, 197.
Terre Haute, 63, 83.
terrestris, Lysimachia, 388.
tessellata, Pyrgus, 39.
Tetraédron minimum, 150.
Tetragoneuria cynosura, 24, 26.
tetrapedia, Crucigenia, 150.
Tetraspora lubrica, 149.
Teucrium canadense, 402, 404.
thalictroides, Caulophyllum, 314.
Syndesmon, 311.
Thalictrum, dasyearpum, 313.
dioicum, 313.
polygamum, 313, 314.
505
506
Thanaos persius, 39.
thapsus, Verbascum, 409.
tharos, Phyciodes, 39.
Thaspium barbinode, 379.
pinnatifidum, 379.
thelypteris, Dryopteris, 201.
thelypteroides, Athyrium, 203.
theo, Heodes, 39.
Thin-grass, 232.
Thistle Family, 427.
Thistle, Canada, 447.
Common Bur, 446.
Roadside, 447.
Russian, 298.
Swamp, 447.
Tall, 447.
Thorn-apple, 308.
Thorn-headed Worms, 101.
Thorn, Downy, 335.
Red-fruited, 335.
Searlet, 335.
Shining, 335.
Three-cornered Bulrush, 186.
Three-leaved Hop-tree, 350 .
Ivy, 354.
Three-seeded Mercury, Virginia, 351.
Three-square, 245.
Thyme-leaved Pin-weed, 368.
Sandwort, 300.
Speedwell, 411.
Thymeleacezx, 370.
thyroides, Polygyra, 74.
Polygyra bucculenta, 74.
thyrsiflora, Naumburgia, 389.
Tick-trefoil, Canadian, 348.
Illinois, 348.
Large-bracted, 342.
Naked-flowered, 342.
Round-leaved, 342.
Panicled, 342.
Pointed-leaved, 342.
Prostrate, 342.
Sessile-leaved, 342.
Showy, 343.
Smooth Small-leaved, 343.
Tickseed, Tall, 440.
Stiff, 440.
Tickseed-sunflower, Tall, 442.
Tiliacee, 364.
Tilia americana, 364.
Timothy, 231.
Tiniaria convolvulus, 296.
Lake Maxinkuckee, Physical and Biological Survey
Tippecanoe Lake, 62, 64, 72, 123.
Tippecanoe River, 15, 16, 21, 42, 43,
A4, 51, 54, -55,..56,.615. -62>> 474,
(2 21d, e000; 00S smolA 49 6 SOs
356, 366.
Tipula, 36.
tinctorium, Galium, 419.
Tithymalopsis corollata, 352.
Tithymalus cyparissias, 352.
tityrus, Epargyreus, 39.
Toad Rush, 261.
Toad-fiax, Bastard, 291.
Blue, 409.
Wild, 409.
Tobacco, Rabbit, 444.
Tobacco-root, 421.
Tokophyra quadripartata, 99.
Tolypothrix tenuis, 148.
_ tomentosa, Spiraea, 330.
Toothed Spurge, 352.
Toothwort, Cut-leaved, 320.
Touch-me-not, Pale, 349.
Spotted, 349.
Wild, 349.
Tovara virginiana, 294.
Toxicodendron radicans, 354.
vernix, 354.
Tracaulon arifolium, 296.
sagittatum, 295, 296.
Tradescantia reflexa, 260.
Trailing Arbutus, 386.
Wild Bean, 346.
Tramea lacerata, 24, 26.
transversum, Musculium, 74.
Tree-of-heaven, 350.
Trefoil, Bean, 392.
Marsh, 392.
tremuloides, Populus, 276.
Triadenum virginicum, 367.
Tribonema bombycinum, 149.
tribuloides, Carex, 250.
tricarinata, Valvata, 73.
trichophyllum, Batrachium, 187, 313.
Trichoptera, Order, 31.
trichosperma, Bidens, 442.
tricoceum, Allium, 262.
tricolor, Hetaerina, 19.
Trientalis americana, 389.
trifida, Ambrosia, 426.
trifidum, Galium, 419.
triflora, Poa, 286.
triflorus, Rubus, 332.
Lake Maxinkuckee, Physical and Biological Survey
trifolia, Staphylea, 356.
trifoliata, Menyanthes, 392.
Ptelea, 31, 350.
trifoliolatus, Nabalus, 426.
Trifolium arvense, 340.
hybridum, 340.
pratense, 340.
repens, 341.
trifolium, Panax, 377.
Triglochin maritima, 219.
Trilliacez, 266.
Trillium erectum, 267.
grandiflorum, 267.
recurvatum, 267.
triloba, Asimina, 306.
trionum, Hibiscus, 366.
Triosteum perfoliatum, 421.
aurantiacaum, 421.
triphyllum, Arisaema, 253.
Sedum, 322.
tripteris, Coreopsis, 440.
tristis, Salix, 281.
trisulea, Lemna, 166.
trivolvis, Planorbis, 73.
troilus, Papilio, 38.
Tropisternus glaber, 34.
True Water-cress, 188, 318.
truncatum, Musculium, 74.
Trumpet-creeper Family, 416.
Trumpet-creeper, 416.
Trumpet-weed, 428.
truncata semiradiata,
15s}
tuberosa, Asclepias, 393.
Castalia, 305.
Mesadenia, 446.
tuberosum, Limodorum, 270.
Tuberous Indian Plantain, 446.
Tubifex, 101.
tubisperma, Carterius, 104.
Tufted Eragrostis, 235.
Loosestrife, 389.
Tulip-tree, 305.
tulipifera, Liriodendron, 305.
Tumble-weed, 225.
Tumbleweed, Kansas, 297, 298.
tumidulum, Spherium, 73.
turgidus, Chrococcus, 141.
Turkey-pea, 379.
Turks-cap Lily, 264.
Turnip, Indian, 253.
turnus, Papilio glaucus, 38.
Micasterias,
507
Turtle, Marsh, 99.
Snapping, 443.
Tussock Sedge, 252.
Twayblade, Loesel’s, 271.
Twig Rush, 196.
Two-leaved Bishop’s Cap, 323.
Mitre-wort, 323.
Twin Lakes, 18, 14, 16, 17, 37, 42, 49,
BY, (55 Tilks alles AySt)S Bele BIskey.
276, 305, 318, 376, 4114.
Twin-berry, 418.
Typhacez, 210.
Typha latifolia, 191, 210.
uliginosa, Solidago, 430.
Ulmaceez, 288.
ulmifolia, Solidago, 430.
Ulmus americana, 288.
fulva, 288.
Ulothrix tenuissima, 156.
zonata, 156.
umbellata, Chimaphila, 384.
Comandra, 291.
Doellingeria, 436.
Strophostyles, 348.
umbellatum, Lilium, 263.
Ornithogalum, 264.
Umbra limi, 258.
umbrosa, Muhlenbergia, 230.
udulata, Quadrula, 44.
Notonecta, 30.
undulatum, Pleurocera, 73.
unguiculatus, Lestes, 19.
uniflora, Monotropa, 384.
Unifolium canadense, 265.
Unio gibbosus, 45, 53.
Unionide, 41.
List of species of, 51.
Upland Bent-grass, 232.
Sumac, Smooth, 3538.
Upper Fish Lake, 56, 638.
Upright Bindweed, 397.
Spotted Spurge, 351.
Urticaceex, 290.
’ Urtica dioica, 290.
gracilis, 290.
urticaefolium, Eupatorium, 428.
Urticastrum divaricatum, 290.
urticifolia, Verbena, 401.
Uses of the Aquatic Flora, 119.
usitatissimum, Linum, 349.
Usnea barbata, 276.
508 Lake Maxinkuckee, Physical and Biological Survey
Utetheisa bella, 39. Verbesina alba, 438.
Utricularia gibba, 196, 414. verna, Collinsia, 410.
intermedia, 195, 414. vernalis, Branchipus, 77.
macrorhiza, 1938, 414. vernix, Toxicodendron, 354.
minor, 196, 414. Vernonia altissima, 427.
Uvularia grandiflora, 266. fasciculata, 427.
Veronica anagallis-aquatica, 410.
Vacearia vaccaria, 301. arvenis, 411.
vacearia, Vaccaria, 301. peregrina, 411.
Vaccinacer, 387. scutellata, 411.
Vaccinium vacillans, 387. serpyllifolia, 411.
vacillans, Vaccinium, 387. verrucosum, Docidium, 153.
vaginaeflorus, Sparobolus, 231. Nostoc, 148.
Vaginicola, 99. versicolor, Ergasilus, 79, 80.
Vagnera racemosa, 265. Iris, 268.
stellata, 265. verticalis, Ischnura, 23.
vaillantii, Galium, 419. verticillata, Ascelepias, 395.
Vaillant’s Cleavers, 419. Chloris, 233.
Goose-grass, 419. Tlex, 354.
Valerianacee, 421. Mollugo, 299.
Valerian Family, 421. Polygala, 350.
Valerian, Edible, 421. Seleria, 249.
Valeriana edulis, 421. verticillatum, Myriophyllum, 175, 375.
validus, Scirpus, 185, 246. verticillatus, Decondon, 191, 370.
Vallisneriacez, 221. Vertigo morsei, 75.
Vallisneria spiralis, 171, 222. Vervain Family, 401.
Vallonia costata, 75. Vervain, Blue, 401.
pulchella, 75. Hoary, 401.
Valvata sincera simplex, 73. Nettle-leaved, 401.
tricarinata, 73. White, 401.
Van Duzee, E. P., 7. Wild, 401.
Vanessa atalanta, 38, 39. vesiculare, Pisidium, 74.
virginiensis, 38, 39. Vesiculina purpurea, 192, 413.
variabile, Pisidium, 74. Vetch, Carolina Milk, 341.
varians, Melosira, 164. Vetchling, Marsh, 344.
Various-leaved Pondweed, 177, 213. Viburnum acerifolium, 420.
Vaucheria, 155. lentago, 420.
Veiny Pea, 344. prunifolium, 420.
velutina, Quercus, 285. vicinum, Sympetrum, 15.
Velvet Leaf, 365. vigilax, Lestes, 20.
Velvety Panic-grass, 227. villosa, Dioscorea, 268.
venosus, Lathyrus, 344. Lactuca, 425.
ventricosa, Lampsilis, 48, 49, 69. vimineus, Aster, 484.
Venus’ Looking-glass, 422. Vinea minor, 392.
Verbascum thapsus, 409. Vine, Love, 397.
Verbenaceez, 401. Wild Potato, 396.
Verbena bracteosa, 401. vinosa, Boyeria, 12.
hastata, 401. Violacez, 368.
stricta, 401. Viola blanda, 369.
urticifolia, 401. fimbriatula, 369.
Large-bracted, 401. hirsutula, 369.
Mullein-leaved, 401. lanceolata, 369.
Lake Maxinkuckee, Physical and Biological Survey 509
Viola palmata, 368.
papilionacea, 369.
pedata, 368.
pubescens, 370.
rostrata, 370.
violacea, Argia, 20.
Lespedeza, 343.
Violet Family, 368.
Violet, Bird’s-foot, 368.
Blue, 368.
Downy Yellow, 370.
Early, 368.
Early Blue, 368.
Hairy Yellow, 370.
Hooded Blue, 369.
Lance-leaved, 369.
Long-spurred, 370.
Meadow Blue, 369.
Ovate-leaved, 369.
Southern Wood, 369.
Sweet White, 369.
Viorna viorna, 314.
viorna, Viorna, 314.
virescens, Carex, 252.
Virgate St. John’s-wort, 366.
virgatum, Hypericum, 366.
Virginia Chain-fern, 202.
Creeper, 363.
Day-flower, 260.
Goatsbeard, 424.
Grape-fern, 198.
Ground-cherry, 407.
Knotweed, 294.
Snakeroot, 292.
Stickseed, 400.
Stonecrop Family, 323.
Stonecrop, 323.
Strawberry, 330.
Three-seeded Mercury, 351.
Virgin’s. Bower, 514.
Water-leaf, 399.
Winterberry, 354.
Virginian Sarsaparilla, Wild, 376.
virginiana, Anemone, 310.
Clematis, 314.
Cracca, 341.
Fragaria, 380.
Gratiola, 410.
Juniperus, 209.
Koellia, 405.
Lappula, 400.
Medeola, 266.
virginiana, Ostrya, 281.
Padus, 337.
Physalis, 407.
Tovara, 294.
virginianum, Botrychium, 198.
Dracocephalum, 404.
Hydrophyllum, 399.
Leptamnium, 415.
virginica, Acalypha, 351.
Anchistea, 202.
Bartonia, 367.
Claytonia, 299.
Commelina, 260.
Cynthia, 424.
Dasystoma, 412.
Krigia, 428.
Leptandra, 412.
Lespedeza, 343.
Myosotis, 400.
Peltandra, 254.
Rhexia, 371.
virginicum, Lepidium, 318.
Pisidium, 74.
Triadenum, 367.
virginicus, Homalocenchrus, 229.
virginiensis, Vanessa, 38, 39.
Virgin’s Bower, Virginia, 314.
virgo, Strobilops, 75.
viride, Chenopodium album, 297.
viridescens, Polygala, 350.
virdiflora, Acerates, 396.
viridis, Chaetochloa, 227.
Euglena, 96.
Eremosphera, 150.
virosa, Lactuca, 424.
Vitacese, 362.
Vitis aestivalis, 362.
bicolor, 362.
cinerea, 362.
cordifolia, 363.
labrusca, 362.
vulpina, 363.
vitreum, Stizostedion, 80.
Viviparus contectoides, 73.
intertextus, 73.
Volvox aureus, 96.
Vorticella chlorastigma, 97.
vulgare, Marrubium, 402.
Tanacetum, 445.
vulgaris, Arcella, 96.
Chara, 159:
Prunella, 408.
510 Lake Maxinkuckee, Physical and Biological Survey
vulgatum, Cerastium, 300.
vulpina, Vitis, 3638.
vulpinoidea, Carex, 249.
Wabash Pig-toe, 51.
River, 48, 63.
Wahoo, 355.
Wake-robin Family, 266.
Wake-robin, Ill-scented, 267.
Prairie, 267.
Walker, Bryant, 70.
walkeri, Amnicola, 73.
Pisidium, 74.
Spherium, 73.
Walkerton, Ind., 236, 290.
Walking-sticks, 27.
Walleyed Pike, 80, 100.
Walnut Family, 272.
Walnut, Black, 272.
White, 272.
walteri, Echinochloa, 225.
Warmouth Bass, 80.
Warsaw, Ind., 56, 87, 144, 310.
Washington, D. C., 77, 197, 236, 256,
2005 259, 298; 506) B07, dibs, S24,
328, 329, 334, 344, 418.
Washingtonia claytoni, 377.
longistylis, 378.
Wasserbluethe, 110.
Wasserbluethe, Time of appearance
of, 110.
Water Boatman, 29.
Bog-rush, 240.
Club-rush, 245.
Hemlock, 381.
Hemlock, Bulb-bearing, 381.
Hoarhound, Cut-leaved, 405.
Lily Family, 304.
Lily, Sweet-scented White, 180, 305.
Maple, 359.
Marigold, 178, 443.
Penny, 33.
Pepper, 295.
Pepper, Mild, 295.
Persicaria, 294.
Pimpernel, 388.
Plantain, American, 219.
Scorpion, 30.
Smartweed, 295.
Speedwell, 410.
Star-grass, 261.
Water-beech, 281.
Water-bug, Giant, 30.
Water-cress, Marsh, 317.
True, 188, 318.
Yellow, 317.
Water-crowfoot, White, 313.
Yellow, 311.
Water-flea, 415.
Water-leaf Family, 399.
Water-leaf, Appendaged, 399.
Virginia, 399.
Water-milfoil, 374.
Spiked, 196, 374.
Whorled, 175, 375.
Water-moss, 302.
Water-parsnip, Hemlock, 380.
Water-plantain Family, 219.
Water-scavenger, 33.
Water-shield Family, 303.
Water-shield, 179, 308.
Water-striders, 30.
Water-thyme, 174.
Water-weed, 174.
Waxwork, 355.
Weak-stalked Club-rush, 196, 245.
Weed, Dyer’s, 431.
Hedge, 319.
Joe-pye, 428.
Weevils, 34.
Western Iron-weed, 427.
Prickly Pear, 370.
Ragweed, 427.
Red Lily, 263.
Rough Golden-rod, 482.
Wheat-grass, Purplish, 288.
Whirligig Beetles, 33.
White Adder’s-tongue, 264.
Ash, 389.
Aster, Small, 434.
Aster, Tall Flat-top, 436.
Avens, 381.
Baneberry, 309.
Beaked-rush, 249.
Bear Sedge, 251.
Blackberry, 401.
Clover, 341.
Elm, 288.
Grass, 229.
Heath Aster, 434.
Hoarhound, 402.
Lettuce, 425.
Maple, 356.
Oak, 286.
Lake Maxinkuckee, Physical and Biological Survey
White Oak, Swamp, 287.
Poplare2io-
Snake-root, 428.
Sweet-clover, 339.
Vervain, 401.
Violet, Sweet, 369.
Walnut, 272.
Wild Potato, 344.
Potato Vine, 396.
Red Plum, 336.
Red Raspberry, 331.
Rhubarb, 292.
Rice, 228.
Rose, 333.
511
Water-crowfoot, 318.
Water Lily, Sweet-scented, 305.
Wild Indigo, Large, 338.
Willow, 279.
White-heart Hickory, 274.
White-lettuce, Glaucous, 426.
White-stemmed Pondweed, 214.
White-top, 435.
Whiteface, 15.
Whitlow-wort Family, 298.
Whorled Loosestrife, 388.
Milkweed, 395.
Milkwort, 350.
Water-milfoil, 175, 375.
Wild Anemone, 310.
Balsam Apple, 421.
Bean, Pink, 348.
Bean, Small, 348.
Bean, Trailing, 346. Bebb’s, 280.
Bergamot, 404. Black, 278.
Black Cherry, 337. Bog, 281.
Black Currant, 326. Common, 279.
Blue Phlox, 398. Dwarf Gray, 281.
Rosemary, 386.
Rye, Nodding, 239.
Sarsaparilla, 315.
Senna, 337.
Snap Dragon, 410.
Strawberry, 330.
Sunflower, Giant, 439.
Timothy, 230.
Toad-flax, 409.
Touch-me-not, 349.
Vervain, 401.
Virginian Sarsaparilla, 376.
Wormwood, 445.
Yam-root, 268.
Yellow Lily, 268.
Williamson, E. B., 12, 16, 28, 24.
Willow Family, 275.
Willow, Beaked, 280.
Celery, 222. Glossy, 279.
Columbine, 309. Heart-leaved, 280.
Crane’s-bill, 348. Livid, 280.
Cucumber, 421.
Geranium, 348.
Peach-leaved, 279.
River-bank, 279.
Ginger, 291. Sage, 281.
Gooseberry, 326. Sandbar, 279.
Holly, 355. Shining, 279.
Indigo, Large White, 338. Silky, 280.
Leek, 262. Swamp, 278.
Liquorice, 419. White, 279.
Lupine, 339. Willow-herb, Linear-leaved, 372.
Madder, 419. Purple-leaved, 372.
Mandrake, 315. \Walleer, 1Dke (Charles 183, 1 10s 15 We
Mint, American, 406. NO:
Mustard, 321. Wilson Snipe, 88.
Nettle, Slender, 290. Wind-flower, 310.
Nettle, Tall, 290. Wing-angled Loosestrife, 371.
Onion, Nodding, 263. Wing-stem, 440.
Parsnip, 378. Winged Pigweed, 297.
Pea-nut, 345. Winona Lake, 87, 103, 112, 115, 116,
Pepper-grass, 318. WoL, él slo, slik,
blz Lake Maxinkuckee, Physical and Biological Survey
Winter Grape, 362.
Winterberry, 354.
Winterberry, Virginia, 354.
Wintergreen Family, 384.
Wintergreen, Chickenweed, 389.
Creeping, 387.
Spicy, 387.
Wire-grass, 233, 237.
Witch-grass, 225.
Witch Hazel Family, 324.
Witch-hazel, 324.
Wolffia columbiana, 167, 258.
Wolffia, Dotted, 259.
Wolffia microscopica, 259.
punctata, 259.
Wolfiella, Florida, 168, 259.
floridana, 168, 259.
Wood Aster, Common Blue, 433.
Betony, 413.
Dropseed, 230.
Nettle, 290.
Reed-grass, 231.
Sage, 402.
Sunflower, Pale-leaved, 440.
Violet, Southern, 369.
Wood-grass, 224, 230.
Wood-lettuce, Hairy, 425.
Red, 425.
Wood-rush, Common, 262.
Wood-sorrel Family, 348.
Wood-sorrel, Yellow, 348.
Yellow Procumbent, 349.
Woodland Dropseed, 230.
Sunflower, 440.
Wool-grass, 248.
Woolly Sedge, 253.
Sweet-cicely, 377.
Worms, 100.
Worms, Gephyrean, 102.
Thorn-headed, 101.
Wormwood, Tall, 445.
Wild, 445.
Wreath Golden-rod, 429.
Wrinkled-leaved Golden-rod, 430.
Xanthium americanum, 427.
Xanthotype crocataria, 39.
Xanthoxalis corniculata, 349.
stricta, 348.
Xyridacee, 259.
Xyris flexuosa, 259.
Yam Family, 268.
Yam-root, Wild, 268.
Yard Rush, 261.
Yard-grass, 233, 261.
Yarrow, 444.
Yellow Adder’s-tongue, 264.
Yellow Birch, Southern, 283.
Catfish, 79, 80.
Hoxtanlee ere
Gentian, 392.
Lily, Wild, 263.
Oak, 287.
Perch, 80, 100.
Pimpernel, 379.
Pond Lily, Large, 304.
Poplar, 305.
Procumbent Wool-sorrel, 349.
River 45 Was Gs Salo AD A Ore ile
Sr, 05 Al, PalBy, AA), Wa eS, Ae
282, 283, 289, 301, 306, 308, 314.
Star-grass, 268.
Sweet-clover, 340.
Violet, Downy, 370.
Violet, Hairy, 370.
Water-cress, 317.
Water-crowfoot, 311.
Wood-sorrel, 348.
Yellow-barked Oak, 285.
Yellow-eyed Grass Family, 259.
Slender, 259.
Yellow-fringed Orchis, 269.
Yellow-root, 308.
Yellowjacket, 40.
Yerba de Tajo, 438.
Young, Leonard, 108, 110, 113.
ypsilophorus, Atax, 61.
zaleta, Polygyra, 74.
Zannichelliacez, 211.
Zanthoxylum americanum, 350.
zebra, Ephithemia, 163.
Zebra Swallowtail, 38.
Ziza aurea, 379.
Zizania aquatica, 228.
Zizaniopsis miliacea, 228.
zonata, Ulthrix, 156.
Zonitoides arboreus, 75.
minusculus, 75.
niticus, 75.
Zoological Park, Washington, D. C.,
201.
Zygnema, 154.
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