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LIBRARY 

OF  THE 

University  of  California. 


GIF^T  OK" 


i \k-^h 

Class 


University  of  California  •  Berkeley 


Digitized  by  the  Internet  Archive 

in  2008  with  funding  from 

IVIicrosoft  Corporation 


http://www.archive.org/details/alaskaharriman13harrrich 


ALASKA 


VOLUME  xin 


HARRIMAN  ALASKA  EXPEDITION 
WITH  COOPERATION  OF  WASHINGTON  ACADEMY  OF  SCIENCES 


ALASKA 

VOLUME   XIII 

LAND  AND  FRESH  WATER 
MOLLUSKS 

BY  WILLIAM   H.  DALL 

HYDROIDS 

BY    C.  C.  NUTTING 


NEW  YORK 
DOUBLEDAY,  PAGE  &  COMPANY 

1905 


Copyright,  1905 

BY 

Edward  H.  Harriman 


^ 


PREFACE 

The  present  volume  comprises  two  papers :  one  on  the  Land 
and  Fresh  Water  Mollusks  of  Alaska,  by  Dr.  Wm.  H.  Dall ; 
the  other  on  the  Hydroids  of  the  Expedition,  by  Prof.  C.  C. 
Nutting.  Dr.  Dall's  paper  has  not  been  previously  published ; 
Professor  Nutting's  appeared  in  the  Proceedings  of  the  Wash- 
ington Academy  of  Sciences  in  May,  1901.  The  number  of 
new  Mollusks  here  described  is  twelve  ;  of  new  Hydroids  twenty. 

C.  Hart  Merriam, 

Editor. 
Washington,  D.  C, 

June  15,  1905. 


(V) 


142370 


CONTENTS 

Paob 

Preface •. v 

List  of  Illustrations ix 

Land  and  Fresh  Water  Mollusks,  by  William  H.  Dall. 

General  discussion  and  results i 

Summary  of  distribution  of  fresh  water  species  in  Alaska 

and  adjacent  regions i 

Table  of  distribution  of  fresh  water  species  according  to 

drainage  systems  now  existing 4 

Summary  of  distribution  of  land  shells  of  Alaska  and  ad- 
jacent regions 7 

Table  of  distribution  of  American  land  shells 8 

Summary  of  the  moUusk  fauna  of  northeastern  Asia 9 

Table  of  distribution  of  northeast  Asiatic  land  and  fresh 

water  shells 14 

Conclusions  in  regard  to  the  Alaskan  fauna 15 

Systematic  catalogue  of    land  and  fresh  water  mollusks  of 

North  America  north  of  the  forty-ninth  parallel 19 

Bibliography 147 

Index  to  genera  and  species 157 

Hydroids,  by  C.  C.  Nutting. 

Introduction 1 75 

Geographic  distribution 1 76 

Systematic  discussion 181 

Bibliography 207 

Volume  Index,.,,,,,,,,,,,,,,,,,,, ,, 235 


(vu) 


ILLUSTRATIONS 

PLATES 

Pacing  pages 
I,  II.  Land  and  Fresh  Water  Mollusks 154,156 

III-XV.  Hydroids 210-234 


TEXT    FIGURES 

Pages 

1-118.  Land  and  Fresh  Water  Mollusks 20-144 


(ix) 


LAND   AND    FRESH    WATER 

MOLLUSKS   OF   ALASKA 
AND    ADJOINING    REGIONS 


NOTE 

The  following  memoir  has  been  prepared  to  bring  together 
and  modernize  the  data  existing  in  the  literature,  and  to  combine 
it  with  the  new  material  obtained  by  the  Harriman  Expedition 
and  such  as  was  accessible  elsewhere  from  the  same  region. 
In  order  to  accomplish  this,  and  because  of  the  uniformity  of 
boreal  faunas  all  round  the  northern  hemisphere,  it  has  been 
necessary  to  examine  the  entire  boreal  fauna  of  North  America, 
Greenland,  and  the  adjacent  parts  of  eastern  Siberia. 

The  material  examined  has  been  that  collected  by  the  Harri- 
man Expedition ;  that  obtained  by  the  writer  during  explora- 
tions in  Alaska  from  1865  to  1885,  and  now  in  the  National 
Museum  ;  collections  from  various  collaborators  of  the  Museum, 
members  of  the  Navy,  the  Revenue  Marine,  and  the  Geological 
Survey  of  the  United  States  ;  and  certain  material  borrowed  for 
examination  from  various  sources.  On  the  whole,  though  the 
collection  is  not  remarkably  large,  it  is  probably  the  largest  and 
most  complete,  for  the  region,  ever  brought  together. 

The  text  figures  have  been  generously  lent  by  the  Smith- 
sonian Institution. 

I  am  indebted  to  Mr.  Bryant  Walker,  Dr.  J.  F.  Whiteaves  of 
the  Dominion  Geological  Survey,  Dr.  H.  A.  Pilsbry,  of  the 
Academy  of  Natural  Sciences,  Philadelphia,  and  numerous 
other  correspondents,  for  advice  and  assistance ;  and  to  the  au- 
thorities of  the  U.  S.  Geological  Survey,  the  Dominion  Geolog- 
ical Survey,  the  Smithsonian  Institution,  and  the  U.  S.  National 
Museum,  for  facilities  for  study  and  access  to  collections,  for 
all  of  which  I  am  deeply  grateful. 

Wm.  H.  Dall. 

Smithsonian  Institution, 
Washington,  D.  C,  Sept.  17,  1904. 


LAND  AND  FRESH  WATER  MOLLUSKS  OF 
ALASKA  AND  ADJOINING  REGIONS 

BY  WILLIAM  HBALET  DALL 
GENERAL  DISCUSSION  AND   RESULTS 

The  first  object  of  this  work  is  to  sum  up  the  known  mollus- 
can  fauna  of  the  land  and  fresh  waters  of  Alaska.  This  has 
involved  an  examination,  not  only  of  the  species  obtained  within 
the  political  boundaries  of  Alaska,  but  also  those  of  the  adjacent 
region  to  the  west,  east,  and  south.  The  result  is  that,  for  North 
America  north  of  latitude  49°  North,  the  work  includes  a  sum- 
mary of  our  present  knowledge  of  the  mollusks,  deduced  in  part 
from  the  literature  and  in  larger  part  from  material  actually 
examined.  To  this  is  added  a  briefer  examination  of  the  mollusk 
fauna  of  the  adjacent  parts  of  eastern  Siberia  which  has  to  some 
extent  modified  that  of  Alaska.  As  a  whole  the  work  may  be 
regarded  as  forming  a  synoptic  manual  of  the  boreal  land  and 
fresh  water  mollusks  of  the  western  hemisphere. 

I.     SUMMARY   OF   THE   DISTRIBUTION  OF    FRESH  WATER   SPECIES 
IN   ALASKA   AND    ADJACENT    REGIONS. 

It  was  thought  best  to  tabulate  the  species  of  rivers  and  lakes 
according  to  the  drainage  systems  in  which  they  are  found. 
Of  course  these  systems  are  not  geologically  ancient,  and  it  is 
even  probable  that  some  existing  species  of  the  Mississippi 
system  were  trapped  by  the  changes  of  level  which,  according 
to  Gen.  G.  K.  Warren,  U.S.A.,  secured,  for  the  Red  River  of 

(I) 


2  LAND    AND    FRESH    WATER    MOLLUSKS 

the  North,  part  of  the  channels  which  earlier  discharged  into 
the  Gulf  of  Mexico  by  way  of  the  Mississippi.  It  is  probable,  for 
the  region  under  review,  that  the  entire  moUuscan  population 
was  exterminated  or  driven  south  during  the  Glacial  epoch,  and 
that  we  now  have  to  do  with  immigrants  from  the  south  whose 
distribution  has  taken  place  since  that  time. 

In  the  following  tables  all  doubtful  species  are  omitted,  so 
that  the  fauna  tabulated,  if  not  complete,  is  at  least  well  estab- 
lished so  far  as  it  goes. 

The  following  areas  are  represented  in  the  successive  columns 
of  the  table : 

Ast'a. — This  column  indicates  those  species  known  also  to 
inhabit  the  eastern  portion  of  Siberia,  Kamchatka,  and  the 
Chukchi  Peninsula,  together  with  the  Commander  Islands, 
which  are  obviously  populated  from  the  Asiatic  shores. 

Tukon. — This  system  includes  the  entire  drainage  basin  of 
the  Yukon  and  the  tundra  north  of  it,  as  well  as  the  area  drained 
by  the  Kuskokwim  River,  or  all  of  Alaska  north,  northwest, 
and  westward  of  the  Alaskan  Range,  as  well  as  the  area  behind 
the  Coast  Ranges  and  between  them  and  the  northward  exten- 
sion of  the  Rocky  Mountains,  drained  by  the  Yukon  and  its 
tributaries. 

Alaska. — This  system  includes  all  of  the  Aleutian  Islands, 
the  area  on  the  Alaska  Peninsula  and  continent  between 
the  Coast  Ranges  and  the  Alaskan  Range  and  the  Pacific 
north  of  latitude  54°.  This  system  and  the  following  one  are 
really  continuous,  the  Alaskan  being  really  only  the  north- 
westward extension  of  that  here  designated  as  the  Pacific 
system. 

Pacific.  —  This  includes  the  coast  drainage  of  British  Colum- 
bia, the  basins  of  the  Fraser  and  Columbia  rivers,  the  coastal 
part  of  the  State  of  Washington,  and  the  northern  part  of  Idaho 
and  Montana  west  of  the  Selkirk  Range  and  its  more  southern 
equivalents  in  the  Rocky  Mountain  region. 

Mackenzie.  —  This  vast  system  includes  the  basin  drained  by 
the  Mackenzie  River  and  its  tributaries,  covering  northwest 
Alberta,  northeastern  British  Columbia,  the  northwestern  two 
thirds  of  Athabaska,  and  the  Mackenzie  district. 


GENERAL    DISCUSSION  3 

Hudson  Bay.  —  This  system,  the  largest  of  all,  comprises  the 
entire  area  draining  into  Hudson  Bay,  including  Keewatin,  the 
southeastern  corner  of  the  Mackenzie  district,  eastern  Atha- 
baska,  the  whole  of  Saskatchewan,  the  southeastern  two  thirds 
of  Alberta,  Assiniboia  and  Manitoba,  the  drainage  area  of  the 
Red  River  of  the  North  in  the  Dakotas  and  northeastern  Minne- 
sota, all  of  Ontario,  Quebec,  and  Ungava  north  and  west  of  the 
*  Height  of  Land.' 

Canada.  —  This  system  comprises  the  drainage  of  the  St. 
Lawrence  and  the  Great  Lakes  south  and  east  from  the  Height 
of  Land,  including  the  island  of  Anticosti. 

Labrador.  —  This  comprises  the  area  draining  into  Ungava 
Bay  and  the  Atlantic  north  of  the  Straits  of  Belle  Isle  and  the 
Height  of  Land,  being  the  Labrador  coast  and  the  northeastern 
part  of  the  Ungava  district  of  the  Dominion  of  Canada. 

A  few  species  are  noted  from  Greenland ;  when  peculiar  to 
Greenland,  or  found  in  Greenland  and  also  on  the  continent, 
the  species  have  been  entered  in  the  Labrador  column  but  dis- 
tinguished by  an  asterisk. 

The  vast  territories  included  in  these  drainage  systems  are, 
it  is  true,  only  partially  and  imperfectly  explored  for  mollusks. 
Yet  certain  portions  of  them  are  tolerably  well  known,  and  the 
uniformity  imposed  on  the  fauna  by  its  high  northern  position 
and  unvaried  conditions  leads  to  the  belief  that  while  much  is 
yet  to  be  known  in  tracing  out  the  details  of  distribution,  little 
is  to  be  expected  in  the  way  of  absolutely  new  species,  even 
from  this  immense  territory  still  to  be  explored.  It  would  be 
rash  to  conclude  that  nothing  new  remains  to  be  found  ;  but  it 
certainly  behooves  us  to  be  moderate  in  our  expectations. 

It  is  probable  that  new  additions  will  be  made  from  among 
the  ranks  of  the  smaller  species,  such  as  Corneocyclas  (or  Pi- 
sidium)^  Vertigo^  and  the  more  minute  HelicidcB.  Perhaps  a 
considerable  number  of  the  more  southern  forms  which  are 
known  to  approach  the  boundary  will  eventually  be  found  to 
pass  beyond  it ;  and  other  additions  to  the  list  will  result  from 
the  more  careful  discrimination  of  similar  or  closely  allied 
species. 


4  LAND   AND   FRESH   WATER   MOLLUSKS 

TABLE     I.       DISTRIBUTION    OF     FRESH     WATER     SHELLS     NORTH 

OF    LATITUDE   49°,    ACCORDING   TO    THE    DRAINAGE 

SYSTEMS    NOW   EXISTING. 


Name  of  Spedei. 


Lymnaea  stagnalis 

Lymnaea  petersi , 

Lymnaea  atkensis 

Lymnaea  megasoma 

Lymnaea  emarginata , 

Lymnaea  binneyi  , 

Lymnaea  preblei  

Lymnaea  columella , 

Lymnaea  randolphi , 

Lymnaea  kirtlandiana  ..,., 

Lymnsea  truncatula 

Lymnaea  humilis 

Lymnaea  desidiosa 

Lymnaea  galbana 

Lymnaea  hSlbolli 

Lymnaea  vahli 

Lymnaea  palustris 

Lymnaea  reflexa 

Lymnaea  catascopium 

Lymnaea  adelinae 

Lymnaea?  perpolita 

Lymnaea  caperata 

Lymnsea  anticostiana 

Planorbis  bicarinatus 

Planorbis  corpulentus  

Planorbis  binneyi 

Planorbis  trivolvis 

Planorbis  campanulatus  .. 
Planorbis  var.  rudentis.... 

Planorbis  exacuous  

Planorbis  var.  megas 

Planorbis  opercularis 

Planorbis  var.  planulatus , 

Planorbis  hirsutus 

Planorbis  var.  deflectus,... 

Planorbis  parvus 

Planorbis  vermicularis 

Planorbis  nathorsti  

Planorbis  arcticus 

Planorbis  umbilicatellus  .. 

Planorbis  crista 

Segmentina  armigera 

Segmentina  christyi 

Physa  heterostropha 

Physa  gyrina 

Physa  ancillaria 

Physa  lordi 

Physa  propinqua 


0* 


GENERAL    DISCUSSION  5 

TABLE     I.       DISTRIBUTION     OF     FRESH     WATER     SHELLS     NORTH 
OF     LATITUDE     49°,    ACCORDING    TO    THE    DRAINAGE 

SYSTEMS  NOW  EXISTING. — Continued. 


Name  of  Species. 


Physa  ampullacea 

Physa  hordacea  

Aplexa  hypnonim , 

Ancylus  rivularis 

Ancylus  parallelus 

Ancylus  fragilis 

Ancylus  kootaniensis 

Goniobasis  plicifera 

Amnicola  limosa ., 

Amnicola  pallida 

Amnicola  emarginata , 

Amnicola  cincinnatiensis . . . 

Lyogyrus  granum  

Pomatiopsis  lapidaria 

Fluminicola  nuttalliana 

Fluminicola  virens  , 

Valvata  tricarinata , 

Valvata  sincera 

Valvata  lewisi 

Valvata  var.  helicoidea 

Valvata  mergella 

Valvata  virens 

Campeloma  decisum 

Lampsilis  ventricosus 

Lampsilis  luteolus 

Lampsilis  borealis 

Lampsilis  radiatus 

Lampsilis  ligamentinus 

Lampsilis  rectus  

Lampsilis  ellipsiformis 

Lampsilis  alatus 

Lampsilis  gracilis 

Strophitus  rugosus 

Anodonta  beringiana 

Anodonta  oregonensis 

Anodonta  nuttalliana  , 

Anodonta  wahlamatensis  ... 

Anodonta  marginata 

Anodonta  implicata 

Anodonta  grandis 

Anodonta  kennicotti 

Anodonta  pepiniana 

Anodonta  kennerlep 

Gonidea  angulata 

Anodontoides  ferussacianus 

Symphynota  costata 

Symphynota  complanata . . . . 
Margaritana  margaritifera... 


o  o 

o  o 

o  o 

o  o 

o  o 

o  o 

o  o 

o  o 

o  o 


6  LAND    AND    FRESH    WATER    MOLLUSKS 

TABLE    I.       DISTRIBUTION    OF     FRESH      WATER     SHELLS     NORTH 
OF    LATITUDE    49°,    ACCORDING    TO    THE    DRAINAGE 

SYSTEMS  NOW  EXISTING. — Continued. 


Name  of  Species. 


Margaritana  var.  falcata , 

Unio  complanatus , 

Quadrula  plicata  , 

Quadrula  undulata 

Quadrula  heros  

Quadrula  lachrymosa  .,., 

Quadrula  rubiginosa , 

Sphser 

Sphaeri 

Sphaer 

Sphaer 

Sphser 

Sphaer: 

Sphaer 

Sphser; 

Sphser 

Sphser: 

Sphaeri 

Sphaer: 

Sphaer: 

Sphaer 

Sphaer 

Sphaer 

Sphser 

Sphser 

Sphaer 


ium  simile 

ium  striatinum 

ium  solidulum 

ium  stramineum 

ium  rhomboideum 

ium  walkeri 

ium  fabale 

ium  occidentale 

ium  patella 

ium  emarginatum 

ium  tumidum 

ium  spokani 

ium  raymondi 

ium  partumeium 

ium  jayanum , 

ium  tenue 

ium  transversum 

ium  truncatum , 

ium  lenticulum 

Corneocyclas  virginica 

Corneocyclas  idahoensis  .... 

Corneocyclas  scutellata , 

Corneocyclas  aequi lateralis . 
Corneocyclas  compressa  .... 

Corneocyclas  variabilis 

Corneocyclas  abdita 

Corneocyclas  ventricosa  .... 

Corneocyclas  rotundata 

Corneocyclas  steenbuchi.... 
Corneocyclas  occidentalis... 
Corneocyclas  ultramontana. 

Corneocyclas  arctica  

Corneocyclas  nivalis 

Corneocyclas  glacialis 

Corneocyclas  pulchella 

Corneocyclas  henslowana ... 


o  o 

o 

o  o 

o 

o  o 

o  o 

o  o 

o  o 

o  o 

o  o 

o  o 

o  o 

o  o 


o» 


GENERAL    DISCUSSION  7 

II.     SUMMARY     OF    THE     DISTRIBUTION     OF    THE     LAND     SHELLS 
OF    ALASKA    AND    ADJACENT    REGIONS. 

I  have  summarized  the  distribution  of  the  fresh  water  shells 
by  drainage  areas,  as  perhaps  the  least  objectionable  method  of 
connecting  the  facts  of  distribution.  But  the  land  shells  require 
a  somewhat  different  treatment,  since  their  distribution  has  noth- 
ing to  do  with  currents  of  water,  though  sometimes  a  snail  may 
be  carried  in  the  spring  freshets  under  the  bark  of  a  floating 
log,  and  by  rare  chance  survive  to  be  stranded  by  the  falling 
waters  somewhere  down  stream.  A  certain  amount  of  move- 
ment of  the  minute  forms  may  result  from  the  distribution  by 
high  winds  of  dead  leaves  and  other  light  material  to  which  the 
smaller  land  shells  are  accustomed  to  adhere.  Pieces  of  ice 
from  smaller  brooks  carried  by  freshets  may  also  convey  a  cer- 
tain distance  and  deposit,  when  stranded  by  falling  water,  pieces 
of  bark  or  leaves  containing  snails  or  their  eggs.  Such  chances 
are  too  rare  to  be  made  much  account  of,  and  doubtless  the  dis- 
tribution of  our  smaller  snails  is  brought  about  in  the  main  by 
the  slow  movement  of  individuals. 

The  Pulmonate  fauna  of  Alaska  is  composed  of  four  elements  : 
contributions  from  the  faunas  of  Asia,  of  the  Pacific  Coast  of 
America,  of  the  Canadian  (or  Hudsonian)  region,  and  of  the 
circumboreal  or  common  subarctic  fauna  of  the  whole  northern 
hemisphere. 

In  tabulating  the  distribution  of  the  species  a  column  may  be 
reserved  for  each  of  these  elements ;  the  circumboreal  column 
being  headed  '  Europe.'  A  column  may  be  reserved  for  Green- 
land, and  another  for  the  approximate  highest  north  latitude 
which  the  species  is  known  to  attain.  This  means  for  the  snail 
not  so  much  differences  of  temperature  corresponding  to  latitude, 
as  differences  of  period  in  activity,  which  diminish  as  one  pro- 
ceeds northward.  Snails  at  Point  Barrow  must  remain  in  a 
state  of  hibernation  at  least  nine  months  in  the  year,  and  I  sus- 
pect that  this  more  probably  brings  a  limiting  strain  on  the 
vitality  of  the  organism  than  would  the  mere  occurrence  at  times 
of  a  specially  low  temperature. 


LAND    AND    FRESH    WATER    MOLLUSKS 


TABLE    II.       DISTRIBUTION    OF   AMERICAN    LAND    SHELLS 

\0 


NORTH    OF    LATITUDE    49'- 


Name  of  Species. 


Helix  hortensis  

Epiphragmophora  fidelis 

Zoogenites  harpa , 

Vallonia  pulchella 

Vallonia  costata 

Vallonia  gracilicosta 

Vallonia  albula 

Vallonia  asiatica 

Polygyra  devia 

Polygyra  columbiana 

Polygyra  townsendiana  . 

Polygyra  germana 

Polygyra  monodon 

Polygyra  albolabris 

Strobilops  labyrinthica  ... 

Bifidaria  armifera 

Bifidaria  contracta 

Bifidaria  holzingeri 

Bifidaria  pentodon 

Pupilla  blandi  

Pupilla  muscorum 

Vertigo  hoppii 

Vertigo  modesta 

Vertigo  columbiana 

Vertigo  gouldii 

Vertigo  ventricosa 

Vertigo  binneyana 

Vertigo  ovata 

Vertigo  arctica 

Cochlicopa  lubrica 

Circinaria  vancouverensis 
Circinaria  var.  chocolata. 

Circinaria  sportella 

Circinaria  var.  hybrida... 

Vitrina  angelicse 

Vitrina  limpida 

Vitrina  alaskana  

Vitrea  radiatula 

Vitrea  nitidula 

Vitrea  binneyana 

Vitrea  indentata 

Euconulus  trochiformis .. 

Zonitoides  nitidus 

Zonitoides  arboreus 

Zonitoides  randolphi 

Zonitoides  minusculus.... 

Zonitoides  milium 

Zonitoides  pugetensis  .... 

Pristiloma  lansingi 

Pristiloma  stearnsii 


4 

< 

1 

< 

■5 
<2 

a 

6 

•0 

a 

H 

0 

0 

0 

0 

0 

0 

0 

0 

0 

0 

0 

0 

0 

0 

0 

0 
0 
0 

0 

0 

0 
0 

0 
0 
0 
0 

0 
0 
0 
0 
0 
0 
0 
0 

0 

0 

0 
0 

0 

0 

0 

0 
0 

0 
0 

0 

0 

0 
0 
0 

0 

0 

0 

0 

0 

0 

0 

0 

0 
0 
0 
0 
0 

0 

0 
0 

0 
0 

0 

0 
0 

0 

0 

0 

0 

0 
0 

0 
0 
0 
0 

0 
0 

0 

0 

0 

0 

0 

0 

0 

0 

0 

0 

0 

0 

0 

0 

0 
0 

0 

0 

0 
0 

0 
0 

0 

0 

54°oc/ 
57  00 
66  00 

54  00 

51  00 

52  20 
50  00 

59  00 
50  00 

60  00 

50  CO 

49  GO 

51  20 

53  00 

51  20 

52  10 

50  00 
52  10 

51  20 

52  ID 

59  00 

70  00 

63  CX) 

57  00 
51  00 
51  25 
50  00 
57  35 
65  15 

71  20 
59  00 
57  00 
59  00 

55  00 

72  00 

54  00 
57  30 
71  20 

61  00 

50  CX) 

50  00 
70  00 
61  00 
61  00 
59  30 
59  00 
50  00 
49  00 
49  00 
59  30 


GENERAL    DISCUSSION 


TABLE    II.       DISTRIBUTION    OF    AMERICAN    LAND    SHELLS 

NORTH  OF  LATITUDE  49^. — Continued. 


Name  of  Species. 


Pristiloma  taylori 

Pristiloma?  arctica  

Agriolimax  agrestis 

Agriolimax  hyperboreus,., 

Agriolimax  berendti 

Prophysaon  andersoni 

Prophysaon  var.  pallidum 
Prophysaon  var.  pacificum 

Prophysaon  humile 

Ariolimax  columbianus 

Pyramidula  solitaria 

Pyramidula  striatella 

Pyramidula  cronkhitei 

Pyramidula  asteriscus 

Oreohelix  strigosa 

Oreohelix  var.  cooperi 

Helicodiscus  lineatus 

Punctum  pygmaeum 

Punctum  clappi 

Punctum  conspectum 

Sphyradium  edentulum 

Succinea  oregonensis , 

Succinea  retusa  

Succinea  hawkinsi 

Succinea  avara 

Succinea  gronlandica  

Succinea  grosvenori 

Succinea  var.  alaskana 

Succinea  rusricana 

Succinea  nuttalliana  ....,..., 

Succinea  obliqua 

Succinea  chrysis 

Siphonaria  thersites 

Onchidium  boreale 

Carychium  exiguum 

Carychium  exile 


o 
o 
o 
o 
o 
o 
o 
o 
o 

o 

(?) 


(?) 


49°oc/ 
71  25 
61  00 
65  00 
49  00 
49  00 

54  45 
49  00 

55  38 
58  CX) 
52  00 
61  00 

61  00 
49  00 
49  30 

49  00 

50  00 
50  00 
49  00 

60  00 
65  20 
49  00 
67  00 
57  00 

62  00 
65  00 

62  00 

63  30 
49  00 

49  00 

61  00 
65  30 
60  30 
60  30 

50  00 
50  00 


III.     SUMMARY    OF    THE     MOLLUSK    FAUNA    OF    NORTHEAST- 
ERN ASIA. 

The  land  shell  fauna  of  the  northeast  extremity  of  Asia  has 
little  individuality,  but  represents  a  mingling  of  the  depauper- 
ated extremes  of  the  faunas  of  northeast  China,  and  of  Europe, 
with  that  series  of  species  which  is  sometimes  called  the  circum- 
polar  or  circumboreal  fauna. 


lO  LAND    AND    FRESH    WATER    MOLLUSKS 

Much  of  the  apparent  poverty  of  the  fauna  may  be  due  to 
insufficient  collecting,  but  even  when  the  most  generous  allow- 
ance for  this  factor  is  made,  it  still  remains  certain  that  the 
molluscan  population  is  far  less  in  variety  than  might  reasonably 
be  expected. 

The  Palearctic  fauna  of  Europe  appears  to  extend  clear 
across  northern  Asia,  losing  a  large  proportion  of  its  species  on 
the  way,  until  (if  the  circumboreal  species  be  excluded)  only 
about  thirty  species  reach  the  headwaters  of  the  Lena  and  the 
barrier  of  the  Stanovoi  Range.  A  very  remarkable  local  fauna 
exists  in  the  great  '  relicten-see '  of  Siberia,  Lake  Baikal,  but 
it  does  not  appear  to  have  tinctured  the  east  Siberian  fresh 
water  fauna  outside  of  that  lake,  to  any  appreciable  extent. 
It  is  possible  that  the  comparatively  recent  emergence  of  a  large 
part  of  eastern  Siberia  from  the  sea,  and  the  presence  of  the 
vast  desert  region  to  the  south  and  west,  may  enter  into  the 
explanation  of  this  sparse  shell  fauna,  as  well  as  of  some  of  the 
peculiarities  of  the  Baikal  faunula. 

Southeast  of  the  Stanovoi  Range  we  find  between  the  moun- 
tains and  the  sea,  the  valley  of  the  Amur  and  several  smaller 
valleys,  such  as  the  drainage  basins  of  the  Ud  and  the  Tugar. 
To  the  southwest  the  sources  of  the  Amur  emerge  from  the 
deserts  of  Gobi  and  Dauria,  and  along  the  line  of  these  water 
courses  has  crept  a  certain  number  of  molluscan  forms  inti- 
mately related  to  or  identical  with  those  of  Mongolia,  China, 
and  the  Orient.  This  forms  the  second  element  of  the  fauna 
of  northeast  Siberia.  The  number  of  purely  endemic  species 
is  remarkably  small,  and  a  portion  of  those  claimed  to  be  of 
this  character  are  probably  mere  local  mutations  of  widespread 
Palearctic  forms  already  known.  Yet  it  would  seem  as  if  a 
more  thorough  exploration  must  add  largely  to  the  species 
now  known,  and  it  is  almost  incredible  that  the  luxuriant 
fertile  valleys  of  Kamchatka  and  the  innumerable  streams 
and  lakes  of  that  country  should  not  be  well  populated  with 
mollusks. 

There  are  few  species  which  seem  to  be  common  to  the  shores 
of  Bering  Sea,  both  Asiatic  and  American,  such  as  Succinea 
chrysis^  Punctum  consfectum  and  Anodonta  beringiana.     There 


GENERAL    DISCUSSION  II 

is  one  local  species,  Eulota  weyrickt,  known  only  from  Sak- 
halin Island  ;  ^  and  another,  Helicigona  subper sonata^  from  the 
valley  of  the  Ud.  Three  forms  of  Vtvtpara  (of  which  two  are 
probably  variants  of  Chinese  forms)  are  the  only  local  species 
of  the  vast  Amur  valley,  or  drainage,  not  known  from  other 
regions.  Nine  specially  Kamchatkan  species  have  been  de- 
scribed, but  about  half  of  them  are  doubtfully  distinct. 

The  total  number  of  land  and  fresh  water  mollusks  known 
from  the  Amurland,  Sakhalin,  Kamchatka,  the  Chukchi  Penin- 
sula, and  the  Asiatic  coast  north  of  the  Amur  and  east  of  the 
Stanovoi  Range,  is  only  eighty-two. 

Of  these,  thirteen  are  circumboreal  species  and  twelve  are 
supposed  to  be  locally  peculiar.  The  remainder  are  distributed 
as  follows : 

Percent 

Europe  and  west  Siberia. 55 

Northeast  China 22 

Common  to  America 13 

Erratic  species 10 

Of  these  erratic  species  a  few  may  be  especially  mentioned. 
Margarttana  margaritifera^  as  is  well  known,  is  absent  from 
the  whole  of  the  great  northern  central  region  of  North  America, 
though  it  appears  in  the  lower  Saskatchewan,  the  sources  of 
the  Missouri,  and  in  eastern  Canada,  while  on  the  Pacific  it 
ascends  at  least  to  latitude  56°  N.  In  eastern  Asia  it  is  known 
from  Kamchatka,  Sakhalin  Island,  the  upper  portion  of  the 
Amur  basin,  and  southern  Mongolia,  but  I  find  no  authoritative 
record  of  it  thence  westward  to  northern  and  middle  Europe. 
Schrenck  did  not  find  it  on  the  lower  Amur. 

Physa  fontinalis  is  reported  from  the  upper  Amur  and  (in  a 
duck's  crop)  the  desert  of  Dauria,  but  is  not  known  from  Siberia 
proper,  though  common  in  Europe.  There  is  an  entire  absence 
of  typical  Physa  throughout  east  Siberia,  so  far  as  reported ; 
and  only  one  species  of  Ancylus  or  Unto  is  known  from  east 
of  the  Yenisei  River  of  Siberia. 

*  In  a  recent  paper  Hugh  Fulton  describes  Eulota  Jllexibilis  and  E.  {Eukadra) 
fiscina  n.  sp.  as  "  probably  "  from  Sakhalin  Island;  but  this  seems  to  me  very 
doubtful  when  we  consider  the  size  of  these  shells  and  the  fact  that  the  warmest 
part  of  Sakhalin  has  a  mean  annual  temperature  of  only  33.4°  F.  and  for  six 
months  of  the  year  the  mean  is  below  the  freezing  point.  The  shells  are  more 
probably  from  Yesso. 


12  LAND    AND    FRESH    WATER    MOLLUSKS 

Aplexa  hypnorum  is  known  from  northern  Europe,  western 
Siberia,  and  the  Chukchi  Peninsula,  but  has  not  been  reported 
from  eastern  Siberia,  or  the  Amur,  though  abundant  in  Alaska, 
and  reaching  on  the  Taimyr  Peninsula  to  73°  30'  north  latitude. 

Zoogenites  harfa  is  known  from  northern  Scandinavia  in 
Europe ;  from  northeastern  America,  the  Hudson  Bay  territory 
and  Southeastern  Alaska,  in  America ;  but  in  Siberia  it  is  re- 
corded only  from  the  easternmost  margin,  the  Chukchi  Penin- 
sula, Bering  Island,  Kamchatka  and  the  lower  Amur.  These 
singularities  of  distribution  must  await  much  more  extended 
knowledge  before  they  can  be  adequately  discussed,  but  it  is 
believed  that  to  some  extent  they  are  due  to  the  transgression 
of  the  sea,  or  of  glacial  ice,  over  part  of  the  area  in  which  a 
species  might  naturally  be  expected  to  occur,  thus  delaying  the 
occupation  of  the  entire  region  by  the  species  concerned. 

In  the  following  table  the  distribution  is  indicated  by  the 
headings  of  the  six  columns.  Varieties  are  not  included  when 
the  typical  form  appears  in  the  table. 

Column  '  Eur.'  includes  those  forms  recorded  as  found  in  Eu- 
rope, including  the  whole  of  European  Russia  and  the  Caucasus. 

Column  '  Lena '  includes  the  drainage  of  the  Lena  and  the 
whole  of  Siberia  from  the  Lena  westward  to  the  Ural  Moun- 
tains. It  should  be  noted  that  a  number  of  species  which  reach 
the  Lena  from  the  west  do  not  cross  the  Stanovoi  Range. 

Column  'Amur '  includes  the  Amur  drainage  basin,  the  Island 
of  Sakhalin,  and  the  smaller  drainage  areas  between  the  Amur 
and  the  Stanovoi  Range. 

Column  'China'  includes  those  forms  which,  having  their 
center  of  distribution  in  China  or  Japan,  extend  their  range  to 
the  drainage  basin  of  the  Amur,  though  often  reaching  only  the 
southern  and  eastern  part  of  it. 

Column  '  Kam.'  indicates  species  belonging  to  the  area  in- 
cluded in  the  Kuril  Islands,  the  Commander  Islands,  Kamchatka 
proper,  the  Chukchi  Peninsula,  and  northeastern  Siberia  east  of 
the  Stanovoi  Range  and  north  of  Aian. 

Column  'Am.'  includes  those  forms  found  in  the  Aleutian 
Islands,  northern  and  northwest  America,  which  also  occur  on 
the  Asiatic  side. 


GENERAL    DISCUSSION  1 3 

The  nomenclature  is  brought  up  to  date  as  far  as  possible. 
The  absence  from  the  list  of  certain  names  which  appear  in  the 
memoirs  of  Schrenck,  Middendorff ,  and  others,  is  only  apparent ; 
they  are  really  present  under  their  revised  names.  I  have 
accepted  Simpson's  determination  of  the  Naiades,  and  retain,  for" 
the  variety  of  Unio  ^ictormii  which  occurs  in  eastern  Siberia,  the 
early  name  adopted  by  Rossmassler  from  Ziegler's  MS.,  rather 
than  the  very  recent  one  which  has  been  proposed  by  Wester- 
lund.  The  list  of  Amurland  moUusks  in  the  Vega  Expedition 
report  includes  several  which  belong  only  to  the  Lena  province 
or  western  Siberia  and  do  not  occur  on  the  Amur. 

The  material  examined  from  which  this  and  the  preceding 
tables  have  been  prepared,  has  been  derived  from  several 
sources.  The  collections  of  the  National  Museum  containing 
the  boreal  shells  upon  which  the  work  of  W.  G.  Binney  was 
partly  founded,  have  been  of  great  help.  I  have  also  had  the 
kind  cooperation  of  Dr.  J.  F.  Whiteaves  of  the  Geological  and 
Natural  History  Survey  of  Canada.  My  own  collections  from 
1865  to  1899  in  Kamchatka  and  Alaska  have  furnished  much 
material.  I  have  also  had  interesting  collections  from  Messrs. 
Randolph,  McGregor,  Stoney,  Hepburn,  Arnheim,  Krause, 
Palmer  and  others  who  have  visited  Alaska  for  pleasure  or  in 
the  Government  service.  The  collections  actually  made  during 
the  Harriman  Expedition  were  more  interesting  than  extensive, 
but  have  helped  considerably,  especially  those  due  to  the 
energy  of  Prof.  Trevor  Kincaid,  of  Seattle,  while  engaged  in 
his  entomological  researches. 


H 


LAND   AND    FRESH    WATER    MOLLUSKS 


TABLE    III.       DISTRIBUTION    OF   NORTHEAST    ASIATIC    LAND 
AND    FRESH    WATER    SHELLS. 


Name  of  Species. 


Zoogenites  harpa  Say 

Vallonia  adela  West 

Vallonia  pulchella  Miiller 

Vallonia  costata  Miiller 

Helicigona  subpersonata  Midd 

Hygromia  hispida  L 

Hygromia  rufescens  Penn 

Hygromia  stuxbergi  West 

Eulota  arcasiana  Crosse 

Eulota  maackii  Gerstf. 

Eulota  middendorffii  Gerstf. 

Eulota  ravida  Benson  

Eulota  schrenckii  Midd 

Eulota  selskii  Gerstf. 

Eulota  weyrichii  Schrenck 

Pupilla  muscorum  L 

Vertigo  alpestris  Alder 

Vertigo  arctica  Wall 

Vertigo  krauseana  Reinh 

Vertigo  borealis  Morel 

Cochlicopa  lubrica  Miiller 

Vitrina  exilis  Morel 

Vitrina  pellucida  Miiller 

Vitrea  radiatula  Alder , 

Euconulus  trochiformis  Montagu  . 

Zonitoides  arboreus  Say 

Limax  agrestis  L 

Limax  hyperboreus  West 

Arion  hortensis  F6r 

Arion  ater  L 

Incilaria  bilineata  Benson 

Pyramidula  ruderata  Studer 

Punctum  conspectum  Bland 

Punctum  ?  floccula  Morel 

Sphyradium  edentulum  Drap 

Succinea  putris  L 

Succinea  chrysis  West 

Lymnaea  stagnalis  L 

Lymnsea  peregra  Miiller 

Lymnsea  auricularia  L 

Lymnsea  ovata  Drap 

Lymnaea  kamchatica  Midd , 

Lymnaea  palustris  Miiller 

Lymnsea  truncatula  Miiller 

Planorbis  limophilus  West 

Planorbis  nitidus  Miiller  , 

Planorbis  contortus  Miiller  

Planorbis  carinatus  Miiller  

Planorbis  borealis  (Lov6n)  West. 

Planorbis  kamchaticus  West 

Planorbis  mSUendorffii  Dyb 

Planorbis  albus  Miiller 


Physa  fontinalis  L !    o 


o 
o 
o 
o 
o 
o 
o 
o 
o 
o 
o 
o 
o 
o 
Sak. 
o 
o 


GENERAL    DISCUSSION 


IS 


TABLE    III.       DISTRIBUTION    OF   NORTHEAST    ASIATIC    LAND 

AND  FRESH  WATER  SHELLS.  —  Continued. 


Name  of  Species. 


i 

J 

i 

< 

a 

o 
o 

o 

o 

o 
o 

o 

o 

o 

o 

o 

o 

o 

o 
o 
o 

o 

? 
? 

o 

0 

o 

o 

o 

o 

o 
o 
o 

o 
o 

o 

o 

o 

o 

o 

o 

o 

o 

o 

o 

o 
o 

o 

o 
o 

o 

o 
o 
o 

o 
o 

o 

o 

o 
o 

o 

o 

o 

o 

o 

o 

o 

o 

o 

Apleza  hj^norum  L 

Carychium  minimum  Muller 

Siphonaria  thersites  Cpr ... 

Valvata  cristata  Muller 

Valvata  piscinalis  Muller 

Valvata  sibirica  Midd 

Valvata  stelleri  Dybowski 

Vivipara  limnaeoides  Schr 

Vivipara  prserosa  Gerstf. 

Vivipara  ussuriensis  Gerstf. 

Bythinia  troscheli  Paasch 

Bythinia  kickxii  Westend 

Bythinia  striatula  Benson 

Melania  cancellata  Benson 

Sphaerium  corneum  L 

Sphserium  lacustre  Miiller 

Sphaerium  asiaticum  Mts 

Comeocyclas  jimnica  Miiller 

Comeocyclas  abdita  Hald 

Comeocyclas  fontinalis  Pfr 

Comeocyclas  sequilateralis  Pr 

Comeocyclas  sibirica  Clessin 

Cristaria  herculea  Midd , 

Cristaria  plicata  Leach , 

Anodonta  beringiana  Midd , 

Anodonta  woodiana  Lea , 

Margaritana  margaritifera  L 

Unio  pictorum  L.  var.  longirostris  RossmSssler 


IV.  CONCLUSIONS  IN  REGARD  TO  THE  ALASKAN  FAUNA. 

The  fauna  of  Alaska,  so  far  as  the  land  and  fresh  water  shells 
considered  in  this  paper  enable  us  to  judge,  is  composite.  The 
mollusks  are  characteristic  especially  of  two,  and  to  a  much 
smaller  extent  of  two  other,  faunas.  The  former  are  limited 
by  topographic  features.  Thus  the  fauna  of  boreal  Canada,  in 
constantly  diminishing  number  of  species,  is  extended  to  the 
northwest,  north  of  the  Alaskan  Range  to  Bering  Sea  on  the 
west  and  the  Arctic  Coast  on  the  north. 

In  like  manner  the  fauna  of  the  northern  part  of  the  Pacific 
States  is  extended  west  of  the  ranges  which  in  the  north  repre- 
sent the  Rocky  Mountains,  and  between  them  and  the  sea, 
northward  into  British  Columbia  and  thence  westward  into 
Alaska,  south  of  the  Alaskan  Range,  until  the  last  representa- 


l6  LAND    AND    FRESH    WATER    MOLLUSKS 

tives  of  the  fauna  disappear  among  the  islands  of  the  Aleutian 
chain.  In  British  Columbia  a  few  species  belong  to  the  valley 
region  between  the  Rockies  and  the  Cascade  Mountains,  and 
do  not  reach  the  sea  coast,  but  these  are  too  few  to  modify- 
perceptibly  the  general  rule,  and  as  a  matter  of  fact  they,  like 
the  valleys  themselves,  soon  disappear  after  crossing  the  49th 
parallel. 

Very  much  the  same  thing  is  true  of  the  birds,  as  I  was  able 
to  demonstrate  some  thirty  five  years  ago  ;  and  even  the  marine 
mollusks  of  the  Alaskan  coast  form  a  somewhat  analogous 
assembly. 

The  other  two  faunas  concerned  are  those  (i)  of  Asia,  or 
rather  eastern  Siberia,  that  part  of  Asia  nearest  to  Alaska,  and 
(2)  the  Holarctic  or  circumboreal  group  of  species  which  are 
common  to  the  entire  boreal  zone  and  characteristic  of  it,  though 
rather  few  in  number. 

In  referring  to  the  Canadian  fauna  it  will  of  course  be  clearly 
understood  that  the  fauna  of  that  part  of  Canada  discussed  in 
this  paper  and  not  the  entire  fauna  of  the  whole  Dominion  is 
meant.  With  this  reservation  we  may  proceed  to  discuss  the 
matter  from  the  statistical  point  of  view. 

One  hundred  and  forty  seven  species  or  strongly  marked 
varieties  are  enumerated  here  from  the  Canadian  region  as 
above  limited,  and  fifteen  other  forms  are  mentioned  which 
though  not  known  to  cross  the  boundary  yet  in  all  proba- 
bility will  eventually  be  found  to  do  so.  By  reference  to 
the  preceding  tables  the  extension  of  each  species  will  be 
found  recorded,  and  the  particular  localities  as  far  as  discov- 
erable are  enumerated  in  the  following  text.  Forty  one  spe- 
cies are  known  from  the  Alaskan  extension  of  this  fauna 
north  of  the  Alaskan  Mountains,  or  characteristic  of  that  part 
of  the  territory.  Half  of  these  are  circumboreal  or  Holarctic 
forms. 

The  fauna  of  British  Columbia,  or  the  British  Columbian 
extension  of  what  I  many  years  ago  designated  the  Oregon- 
ian  fauna,  comprises  seventy  five  species,  so  far  as  known,  to 
which  in  all  probability  should  be  added  some  thirty  eight  which 
are  known  to  approach  the  parallel  of  49^  from  the  south  and 


GENERAL    DISCUSSION  1 7 

whicn  probabl}'  cross  it,  making  a  probable  total  British  Colum- 
bian fauna  of  one  hundred  and  thirteen  forms.  Considering 
the  very  small  area  occupied  by  this  assembly,  when  compared 
with  the  vast  expanse  populated  by  the  Canadian  fauna,  the 
number  is  notable.  Doubtless  in  both  cases  future  exploration 
will  add  a  reasonable  number  not  now  enumerated  or  still 
undescribed  by  naturalists. 

The  contributions  from  the  Columbian  assembly  to  the  fauna 
of  Alaska  south  of  the  Alaskan  and  west  of  the  Cascade  Ranges 
comprise  thirty  five  known  and  six  probable  species,  a  total  of 
forty  one  forms  probably  inhabiting  the  area  referred  to.  Some 
of  these,  however,  are  common  to  northern  Alaska  also,  making 
the  proper  deduction  for  which  we  find  sixty  five  species  of  land 
and  fresh  water  mollusks  known  to  inhabit  the  territory  of 
Alaska,  with  six  or  seven  more  which  are  likely  with  further 
exploration  to  be  credited  to  it  in  addition  to  those  now  known, 
even  if  no  undescribed  species  turn  up. 

The  vast  unexplored  areas,  the  uncertainties  connected  with 
lists  of  obsolete  names  and  doubtful  identifications,  the  doubt 
as  to  what  may  be  considered  specific  limits  in  groups  of  noto- 
rious variability,  and  especially  the  frequent  absence  of  specimens 
from  which  better  deductions  might  have  been  drawn  than  were 
possible  from  the  extant  literature,  have  all  contributed  to  the 
difficulties  under  which  this  memoir  has  been  prepared.  Those 
who  have  done  work  on  similar  lines  will  understand,  and  will 
view  without  undue  severity,  the  imperfections  which  the  author 
only  too  well  realizes,  and  yet  which  it  was  out  of  his  power, 
in  the  present  state  of  our  knowledge,  to  avoid.  It  is  hoped, 
however,  that  this  summary  will  make  the  path  somewhat  easier 
for  those  who  follow  him,  and  contribute  a  reasonable  share  to 
the  better  appreciation  of  the  facts  of  Nature  of  which  it  treats. 
And  if,  among  the  hardy  explorers  of  whom  our  neighbors  of 
Canada  are  justly  proud,  this  paper  serves  to  stimulate  an 
increased  interest  in  the  subject,  the  author  will  feel  that  his 
endeavors  are  amply  repaid. 


SYSTEMATIC  CATALOGUE  OF  LAND  AND  FRESH 

WATER  MOLLUSKS  OF  NORTH  AMERICA 

FROM  THE  REGION  NORTH  OF  THE 

FORTY-NINTH  PARALLEL. 

The  following  annotated  catalogue  is  intended  to  contain  a 
list  of  all  the  species  known  to  inhabit  the  designated  region, 
with  the  addition  of  a  few  which  approach  the  boundary  so  closely 
that  it  is  highly  probable  that  on  further  search  their  range  will 
be  found  to  cross  it.  Names  of  species  belonging  to  the  latter 
category  are  preceded  by  an  asterisk. 

It  is  intended  that  the  synonymy  which  follows  the  name 
shall  exhibit  references  to  the  original  description  of  the  species, 
to  a  good  figure,  and  to  the  work  in  which  the  synonymy,  if  at 
all  complicated,  may  be  found  most  fully  set  forth.  The  syn- 
onymy of  some  of  the  genera  mentioned  seeming  to  be  in  great 
need  of  elucidation,  an  attempt  has  been  made  to  clear  it  up. 
In  other  cases,  where  the  work  has  elsewhere  recently  been 
done,  the  generic  name  and  authority  alone  are  cited.  For  the 
HelicidcB  and  associated  forms  I  have  depended  upon  the  ar- 
rangement of  Dr.  H,  A.  Pilsbry,  the  acknowledged  master  of 
the  subject ;  and  for  the  Naiades,  in  like  manner,  on  the 
*  Synopsis '  of  Mr.  Chas.  T.  Simpson.  Some  of  the  other 
groups  I  had  previously  worked  up  elsewhere,  and  have  utilized 
the  results  in  this  catalogue. 

After  the  synonymy  it  has  been  attempted  to  state  the  range 
of  the  species  geographically,  in  general  terms.  This  state- 
ment is  followed  by  a  citation  of  special  localities  within  the 
designated  region  from  which  the  species  has  been  reported,  and 
in  those  cases  in  which  the  writer  has  verified  the  report  by  the 
examination  of  specimens,  the  name  of  the  locality  is  followed 
by  an  exclamation  mark. 

These  data  are  exemplified  or  explained  by  notes  following 
the  details  of  geographical  distribution  in  a  separate  paragraph. 

The  data  in  many  cases  have  been  taken  from  the  literature, 
a  bibliography  of  which  concludes  this  paper ;  and  it  follows 
that  the    resent  writer  assumes  no  responsibility  for  the  identifi- 

(19) 


20  LAND   AND    FRESH   WATER   MOLLUSKS 

cation  of  species  so  derived.  Usually,  however,  there  is  no 
particular  reason  for  doubting  the  accuracy  of  these  identifica- 
tions. It  has  not  seemed  necessary,  in  most  cases,  to  cite  the 
authority  for  the  locality,  a  course  which  would  have  unduly 
increased  the  bulk  and  diminished  the  clearness  of  the  distribu- 
tional statement.  The  authority,  as  a  rule,  can  easily  be  found 
by  reference  to  the  bibliography.  In  a  few  cases,  however,  it 
has  seemed  desirable  to  include  in  parentheses  the  authority  for 
the  locality  cited,  especially  when  the  latter  seemed  unusual  or 
debatable. 

Family  HELICID^. 

Genus  Helix  (L.)  Pilsbry. 

Helix  (Cepaea)  hortensis  MuUer. 

Helix  hortensis  Muller,  Verm.  Terr,  at  Fluv.,  ii,  p.  52,  1774. — Binney, 
Land  and  Fw.  Sh.  N.  Am.,  I,  p.  181,  figs.  317-320,  1869. 

Helix  subglobosa  Binney,  Boston  Joum.  Nat.  Hist.,  i,  p.  485,  pi.  xvi, 
1867. 

Range.  —  Europe  from  Hungary  to  the  Atlantic  between  middle 
Scandinavia  and  the  Pyrenees,  northeastern  border  of  North  America. 
Labrador;  Newfoundland;  Anticosti  Island!  Barachois,  Gaspe ; 
Cape  Breton  Island  !  ^  Halifax  !  Casco  Bay,  Maine  !  shore  of  Cape  Ann 
and  adjacent  islets,  Mass.  !  Nantucket  Island !  Pleistocene  deposits 
near  Portland,  Maine ! 

A  single  specimen  was  once  found  in  Greenland,  but  was  doubtless 
imported  accidentally.  The  prevalent  type  is  light  yellow,  without  or 
with  only  faint  traces  of  bands.  The  former  is  Binney 's  H.  subglobosa. 
The  wide  distribution  of  the  species,  often  on  un- 
inhabitable islets  off  a  coast  little  frequented,  and  its 
presence,  which  I  have  verified,  in  the  glacial  Pleis- 
tocene of  Maine,  tend  to  confirm  the  view  that  it  is 
a  prehistoric  immigrant  if  an  immigrant  at  all. 
Fig.  I.  Helix  I  have  seen  most  of  the  commoner  varieties  which 
hortensis  var.  ^j-g  prevalent  in  Europe,  but  it  is  obvious  to  the  col- 
su  go  osa  m-  ig^tor  that  the  brighter  colored  types  with  sharply 
define  ddark  bands  form  an  insignificant  proportion 
of  the  American  specimens  ;  while  the  shells  as  a  whole  seem  smaller 
than  the  average  dimensions  of  European  specimens. 

>  The  exclamation  point  indicates  that  specimens  from  this  locality  have  been 
seen  by  me  and  verified  as  correctly  identified. 


FAMILY    HEL.ICID-«  21 

Helix  (^Ariantd)  arbustorum  L.  has  been  noted  as  an  introduced 

species,  at  St.  John,  Newfoundland,  just  outside  of  our  region,  by 

Whiteaves. 

Genus  Epiphragmophora  Doering. 

Epiphragmophora  fidelis  Gray. 

Helix  fidelis  Gray,  Proc.  Zool.  Soc.  Lond.,   1834,  p.  67  ;  Conch.  Cab.,  2d 

ed.,  Mon,  Helix,  p.  321,  pi.  LVii,  figs.  12,  13. 
Helix  nuttalliana  Lea,  Trans.  Am.  Phil.  See,  vi,  p.  88,  pi.  xxiii,  fig.  74, 

1839. 
Epiphragmophora  fidelis  Vws&BX,  Class.  Cat.  N.  Am.  Landsh.,  p.  4,  1897. 

Range.  —  Northern  California  to  Sitka,  Alaska. 

Sumas  Prairie,  Fraser  River  valley,  B.  C.  (common  to  6,000  ft.,  J. 
K.  Lord)  ;  Chilliwak  Lake,  B.  C. ;  Victoria  !  Nanaimo  !  Comox  !  on 
Vancouver  Island;  Growler  Cove,  Broughton  Strait;  Union  Bay! 
False  Bay,  Lasqueti  Id. ;  Malaspina  Inlet ;  N.  point  Texada  Island, 
British  Columbia ;  Sitka,  Alaska  ! 

The  Sitkan  and  Columbian  specimens  are  apparently  not  markedly 
different  from  those  collected  further  south,  and  pass  through  the  same 
color  variations.  If  there  is  any  difference  it  is  that  the  northern  speci- 
mens are  a  little  smaller  and  exhibit  no  tendency  to  pilosity.  The 
two  specimens  obtained  at  Sitka  were  found  near  the  Hot  Springs. 
There  is  no  evidence  in  regard  to  the  distribution  of  the  species  north 
of  Sitka,  but  it  would  not  be  surprising  if  it  were  eventually  found  to 
extend  on  the  outer  islands  as  far  north  as  Cross  Sound. 

Genus  Zodgenites  Morse. 

This  group  has  been  united  with  the  Acanthinula  of  Beck,  of 
which,  it  would  seem,  little  is  known  but  the  shell,  while  we  have, 
thanks  to  Morse,  a  very  satisfactory  account  of  our  mollusk.  I  prefer 
therefore  to  defer  any  consolidation  with  Acanthinula  until  it  is  shown 
to  be  necessary.  The  information  to  be  had  from  Moquin  Tandon  in 
regard  to  Acanthinula  aculeata  is  unsatisfactory  and  insufficient. 
Westerlund  (1902)  has  proposed  a  genus  Aulaca  to  contain  both 
(prior)  genera ! 

Zobgenites  harpa  Say. 

Helix  harpa  Say,  Rep.  Long's  Exped.,  11,  p.  256,  pi.  xv,  fig.  i,  1824  ;  Bin- 

ney's  Say,  p.  29,  pi.  lxxiv,  fig.  i. 
Pupa  costulata  Mighels,  Proc.  Boston  Soc.  Nat.  Hist,  i,  p.  187,  1844. 
Bulimus  harpa  Pfeiffer,  Conch.  Cat.,  ed.  11,  Bulimus,  p.  305,  pi.  lx,  figs. 

17-19. 
Helix  amurensis  Gerstfeldt,  M6m,  des.  Sav.  €tr.,  ix,  p.  517,  pi.  i,  figs. 

26,  a-c,  1859. 


22  LAND    AND    FRESH    WATER    MOLLUSKS 

Zoogenites  harpa  MoRSE,  Journ.  Portland  Soc.  Nat.  Hist.,  i,  p    32,  pi.  I,  figs. 

1-14,  1864;  Am.  Nat.,  i,  p.  608,  figs.  50-51,  1868. 
Acanthinula  harpa  Binney,  Land  and  Fw.  Sh.  N.  Am. ,  i ,  p.  1 56,  figs.  267-9, 

1869  ;  Bull.  U.  S.  Nat.  Mus.  No.  28,  p.  185,  figs.  181-184,  1885. 
Zoogenetes  harpa  auct.  plur. 

Range. —  Northwestern  Scandinavia,  northeastern  America,  British 
America  near  Hudson  Bay,  Southeastern  Alaska,  and  the  easternmost 
margin  of  Siberia. 

Konyam  Bay,  eastern  Siberia;  Avacha  Bay,  Kamchatka  !  Bering 
Island,  Commander  group  ;  lower  Amur  River  region.  Klehini,  Chil- 
kat  Inlet  and  valley,  Alaska ;  English  River,  Manitoba !  Moose 
Factory  !  Hudson  Bay  ;  Minnesota  ;   Gaspd  ;  New  England  ;  etc. 

The  peculiarities  of  the  distribution  of  this  curious  little  mollusk  are 
referred  to  in  the  general  discussion  of  the  fauna  of  northeastern  Asia. 

Genus  Vallonia  Risso. 

Vallonia  Risso,   Hist.  Eur.   Mer.,  iv,  p.    10 1,    1826;    V.  rosalia  Risso,  pi.  3, 

fig.  30,  =  Helix  costata  Miiller. 
Zurama   Leach,    Proofsheets,   p.  108,    1819. — Turton,  Man.,   p.  64,  1831  ; 

Gray's  Turton,  p.  141,  1840. — Leach,  Syn.  Moll.  Gt.  Brit.,  p.  ^^,  1852  ; 

H.  pulchella  Miiller. 
Amplexis  Brown,  111.  Conch.  Gt.  Brit,  expl.  pi.  xli,  figs.  75-79.  1827;  H. 

pulchella  Miiller. 
Ampiextts  Brown,  op.  cit.,  2d  ed.,  p.  45,  1844. 
CMlostoma  (sp.)  Fitzinger,  Syst.  Verz.,  p.  98,  1833. 
Circinaria  (sp.)  Beck,  Index  Moll.,  p.  23,  1837. 
Glaphyra  Albers,  Heliceen,  p.  87,  1850. 
Lucena  MoQUiN  Tandon,  Hist.  Moll.  Terr,  et  Fluv.  France,  li,  pp.  98,  140, 

1855  ;  not  of  Oken,  1815,  or  Hartmann,  1821. 

Vallonia  pulchella  Miiller. 

Helix  pulchella  Muller,  Verm.  Terr.,  11,  p.  30,  1774. — Binney,  Boston 
Journ.  Nat.  Hist.,  ill,  p.  375,  pi.  ix,  fig.  2,  1840.— W.  G.  Binney,  Land 
and  Fw.  Sh.  N.  Am.,  i,  p.  157  {ex  parte),  figs.  270-1,  1869. 


Fig.  2.      Vallonia  pulchella,  \. 

Helix  minuta  Say,  Journ,  Acad.  Nat.  Sci.  Phila.,   i,  p.  123,  1819. — Morse, 

Am.  Nat.,  i,  p.  544,  fig.  39,  1867. 
Helix paludosa  DaCosta,  Brit.  Conch.,  p.  59,  1778. 
Vallonia  minuta  Morse,  Journ.   Portland  Soc.   Nat.   Hist.,  i,  p.  21,  figs.  54- 

56,  pi.  viii,  fig.  57,  1864. 


FAMILY    HELICID^ 


23 


Range.  —  Europe;  North  Africa,  southern  and  western  Siberia 
to  the  Amur ;  Madeira ;  the  Azores  ;  eastern  North  America  from 
Manitoba  to  Florida  and  Montana  to  Nova  Scotia. 

Manitoba,  at  Winnipeg  and  Pembina ;  north  to  the  Saskatchewan 
(Richardson).     Introduced?  in  California. 

Although  Risso's  figure  of  V.  rosalia  represents  a  perfectly  smooth 
shell,  his  diagnosis  calls  for  one  with  elevated  lamellae  ;  it  is  probable 
therefore  that  he  regarded  the  present  species  and  V.  costata  as  varie- 
ties of  a  single  species. 

Vallonia  costata  Muller. 

Helix  costata  Muller,  Verm.  Terr.,  11,  p.  31,  1774. 
Helix  crenella  Montagu,  Test.  Brit.,  i,  p.  441,  pi.  xili,  fig.  3,  1804. 
Helix  pulchella  var.    Rossmassler,  vii,  p.  6,    fig.   439,    1838. —  Fi:RUSSAC, 
Hist.,  pi.  LXix  E,  figs.  15-17,  1821. 

Range.  —  With  V.  pulchella  in  Europe  and  Asia ;  in  America  in 
the  northern  States  and  northward  from  Kansas  and  Colorado. 

Manitoba  (Hanham). 

This  species  has  been  so  constantly  confused  with  the  other  costate 
species  and  with  V.  pulchella  that  it  is  hardly  practicable  to  determine 
its  true  range  from  the  literature. 

Vallonia  gracilicosta  Reinhardt. 

Vallonia  gracilicosta  Reinhardt,  Sitz.  Ber.  der  Ges.  Naturf.  Freunde  zu  Ber- 
lin, 1883,  No.  3,  p.  42.     Little  Missouri. 

Range.  —  Rocky  Mountain  region,  westward  and  northward  from 
the  upper  Missouri. 

Manitoba,  at  Winnipeg ;  in  Alberta  at  Laggan.  Red  Deer  Olds  and 
McLeod. 

Easily  recognized  by  its  very  prominent,  not  crowded,  very  oblique 
lamellae . 

Vallonia  albula  Sterki. 

Vallonia  albula  Sterki,  Proc.  Acad.  Nat.  Sci.   Phila,,  1893,  p.   263,  pi.  viii, 
figs,  D,  o;  Nautilus,  ix,  p.  17,  May,  1895. 

Range.  —  Eastern  Canada  to  British  Columbia. 
Quebec  ;   Manitoba  ;  Vancouver  Island. 

Vallonia  asiatica  Nevill. 

Helix  costata  var.    asiatica  Nevill,   Sci.  Results  2d  Yarkand  Mission,  p.  4, 

No.  7,  1877. 
Vallonia  asiatica  Reinhardt,  Sitz.  Ber.  der  Ges.  Naturf.  Freunde  zu  Berlin, 

1883,  No.  3,  p.  42. 

Range.  —  Central  Asia,  Tibet.     Alaska. 


24  LAND    AND    FRESH    WATER    MOLLUSKS 

Pyramid  Island,  Lynn  Canal,  Alaska, _/?</«  Reinhardt. 

This  form,  collected  by  Dr.  Krause,  was  identified  by  Dr.  Rein- 
hardt with  Nevill's  species  and  is  included  here  solely  on  his  authority, 
as  I  have  not  seen  specimens. 

Genus  Polygyra  Say. 
Polygyra  devia  Gould. 

Helix  devta  GovLT>,  Proc.  Boston  Soc.  Nat.  Hist.,  ii,  p.  165,  1846. — Binney, 

Land  and  Fw.  Sh.  N.  Am.,  i,  p.  152,  fig.  259,  1869. 
Helix  baskervillei  Pfeiffer,  Proc.  Zool.  Soc.  London,  p.  130,  1849. — Reeve, 

Conch.  Icon.,  Helix ^  fig.  684,  1852. 
Polygyra  devia  Pilsbry,  Class.  Cat.  N.  Am.  Landsh.,  p.  11,  1897. 

Range.  —  Washington  and   Idaho,  north   into    British   Columbia. 
Sumas  Prairie,  B.  C. ;  Esquimalt,  Vancouver  Island. 

Polygyra  columbiana  Lea. 

Helix  Columbiana  Lea,  Trans.   Am.  Phil.  Soc,  vi,  p.  89,  pi.  xxiii,  fig.  75, 

1839. —  Binney,  Terr.  Moll.,  11,  p.  169,  pi.  v,  185 1. 
Helix  labiosa  Gould,  Proc.   Boston  Soc.  Nat.  Hist.,  11,  p.    165,  1846  ;  Expl. 

Exp.  Moll.,  p.  6"],  fig.  35,  1852. 
Polygyra  columbiana  Pilsbry,  Class.  Cat.  N.  Am.  Landsh.,  p.  11,  1897. 

Range.  —  Monterey  Bay,  California,  to  Yakutat  Bay,  Alaska,  in  the 
moist  wooded  region  west  of  the  Rocky  Mountains. 

Mountains  of  Idaho,  western  Montana  and  Washington  ;  Vancouver 
Island  at  Victoria  !  Nanaimo  and  Nootka  ;  British  Columbia  mainland 
on  banks  of  Fraser  River  (Lord)  and  Skeena  River !  (Osgood)  ;  Har- 
bledown  and  Pender  Islands,  Johnstone  Strait ;  Union  Bay !  Port 
Simpson;  and  Cumshewa  Inlet,  Queen  Charlotte  Islands  !  B.  C. ;  in 
Alaska  at  Cape  Fox  !  Annette  Island,  Killisnoo,  Sitka  !  Lynn  Canal ; 
Biorka  Island  !  Chilkat  valley  !  Lituya  Bay  !  Yakutat ! 

There  are  several  varieties  of  this  widespread  and  familiar  species. 
First,  the  type,  subconic  rather  elevated  and  small,  with  narrow  re- 
flexed  lip.  Lea's  specimen  was  decorticated  and  showed  no  signs  of  the 
hairs  with  which  the  shell  is  usually  covered,  but  this  was  accidental ; 
some  specimens  normally  show  hardly  a  trace  of  the  hairs  which  are 
usually  so  conspicuous.  The  second  variety,  P.  labiosa  Gould,  is 
larger,  more  depressed  relatively,  with  a  broader,  somewhat  flexuous 
reflected  lip.  This  form  is  more  prevalent  in  the  interior  of  Washing- 
ton, Idaho,  etc.,  and  more  often  has  a  parietal  tooth  or  trace  of  a  tooth. 
The  variety  santacruzensis  is  in  form  more  like  the  type  but  much 
smaller,  thin,  lighter  colored,  with  a  sparser  pelage,  and  about  half 
the  specimens  have  a  trace  of  a  parietal  tooth,  while  in  a  lot  of  about 
seven  hundred  columbiana.,  from  Sitka,  I  found  only  one  specimen 


FAMILY    HELICID^  2$ 

which  had  any  parietal  tooth.  The  mountain  forms  from  California, 
if  not  hybrids,  are  so  verj-  different  from  the  hairy  coast  or  lowland 
shells  that  one  is  tempted  to  regard  them  as  distinct ;  they  frequently 
are  rough,  hairless,  with  heavy  lip  and  well  marked  parietal  tooth.  A 
young  specimen  of  the  typical  form,  collected  near  Yakutat  Village 
by  the  Harriman  Expedition,  is  reversed. 

Some  specimens  of  this  and  another  species,  both  of  which  are  con- 
fined to  wooded  regions  so  far  as  authentically  known,  were  once  sent 
me  as  from  a  point  considerably  north  of  Yakutat  and  from  the  tree- 
less region.  I  do  not  believe  these  shells  were  correctly  labelled,  and 
hence  have  not  included  them  in  the  list  of  localities.  My  own  im- 
pression is  that  the  extension  northward  of  this  species  and  Circinaria 
vancouverensis  has  been  prevented  by  the  wide  stretch  of  glacial  area 
just  north  and  west  from  Yakutat  Bay.  I  have  searched  for  this 
species  at  Prince  William  Sound  and  Cook  Inlet,  in  suitable  situa- 
tions, but  without  success. 

Polygyra  townsendiana  Lea. 

Helix  townsendiana  Lea,  Trans.  Am.  Phil.  Soc,  vi,  p.  99,  pi.  xxill,  fig.  80, 
1839.  —  BiNNEY,  Land  and  Fw.  Sh.  N.  Am.,  I,  p.  164,  fig,  285,  1869. 

Range. — Puget  Sound  region  and  south  (to  northern  Califor- 
nia?). Seattle,  Wash.;  Lake  Chilliwak  and  Sumas  Prairie,  British 
Columbia. 

Eastward  from  the  moist  coast  region  the  following  species  oc- 
curs and  is  sometimes  regarded  as  a  depauperate  form  of  P.  town' 
sendiana . 

*  Polygyra  ptychophora  Brown. 

Helix  ptychophora  h..  D.  Brown,  Joum.  de  Conchyl.,  3me  Ser.,  x,  p.  392, 

Oct.,  1870. 
Arionta  townsendiana  var.  ptychophora,  Binney,  Man.  Am.  Landsh.,  p.   129, 

fig.  102,  1885. 

Range.  —  Western  Montana  (at  Deer  Lodge)  westward  through 
northern  Idaho  to  Spokane,  Wash.,  and  to  The  Dalles,  in  northern 
Oregon. 

It  is  possible  that  this  form  may  hereafter  be  found  on  the  northern 
side  of  the  boundary. 

Polygyra  germana  Gould. 

Helix germana  Gould,  U.  S.  Expl.  Exp.,  Moll.,  p.  70,  fig.  40,  a-c,  1852. 
Stenotrema  germanum  (Gould)  Binney,  Man.  Am.  Landsh.,  p.  114,  fig.  82, 
1885. 
Range. — Northern  California,  through  the  Puget  Sound  region  to 
British    Columbia. 


26 


LAND    AND    FRESH   WATER    MOLLUSKS 


Astoria,  Oregon!  Victoria,  Vancouver  Island;  Chilliwak  Lake, 
British  Columbia. 

A  variety  megasonia^  more  than  four  times  the  size  of  the  typical 
germana^  but  otherwise  quite  similar,  is  occasionally  found ;  some 
from  northern  California  (Stearns)  are  in  the  National  Museum. 

Polygyra  monodon  Rackett. 

Helix  monodon  Rackett,  Trans.  Linnean  Soc,  xili,  p.  42,  pi.  v,  fig.  2,  1822. 
—  Morse,  Am.  Nat.,  i,  p.  151,  figs.  12,  13,  1867. — 
BiNNEY,  Land  and  Fw.  Sh.  N.  Am.,  i,  p.  120,  figs.  200- 
205,  1869. 

Range.  —  Eastern  United  States,  east  of  the  plains 

iG-  3-      oy-     region,    from   Texas   to   Minnesota  and    northward. 
gyra     monodon      _  °         _,  ^  -r.       . 

Rackett.  Moose  Factory,  James  Bay  ! 

Polygyra  albolabris  Say. 

Helix  albolabris  Say,  Nicholson's  Encycl.,  ist  Am.  ed.,  pi.  i,  fig.  i,  1817  ;  Am. 
Conch.,  II,  pi.  XII,  1831. — Morse,  Am.  Nat.,  i,  p.  6,  pi.  i,  figs,  i-ii, 
1867.  —  BiNNEY,  Land  and  Fw.  Sh.  N.  Am.,  i,  p.  136,  figs.  229-232, 
1869. 

Range.  —  Eastern  United  States,  from  Georgia  and  Arkansas  north- 
ward to  the  Saskatchewan. 


Figs.  4-6.     Polygyra  albolabris  Say,  \ 


Lake  Superior  region ;  Lake  Winnipeg,  Manitoba ;  and  northward 
to  the  Saskatchewan  River  (Richardson). 


FAMILY    PUPID^ 


27 


Fanuly  PUPID^. 
Genus   Strobilops   Pilsbry. 


7.  Animal  from  above.  8.  f .  9.  Showing  internal  lamellae. 

Figs.  7-9.     Strobilops  labyrinthica  (magnified). 

Strobilops  labyrinthica  Say. 

Helix   labyrinthica   Say,   Joum.  Acad.    Nat.  Sci.    Phila.,   i,    p.    124,    181 7. 

— Morse,  Am.  Nat.,  i,  p.    145,  figs.  41-42,  1867. — Binney,  Land  and 

Fw.  Sh.  N.  Am.,  i,  p.  84,  figs.  150-154,  1869. 
Strobila  labyrinthica  Morse,  Joum.  Portland  Soc.  N.  Hist.,  i,  p.   26,  figs.  64- 

67,  pi.  II,  fig,  12,  a-b,  pi.  VIII,  fig.  68,  1864. 
Strobilops  Pilsbry,  1892,   new  name  for  Strobila  Morse, 

1864,  not  Sars,  1835. 

Range. — Eastern  United  States,  from  Texas  north- 
ward to  British  America. 

Carberry,  Manitoba ;  Moose  Factory,  James  Bay  ! 


Genus  Bifidaria  Sterki. 
Bifidaria  armifera  Say. 

Pupa  armifera  Say,  Joum.  Acad.  Nat.  Sci.  Phila.,  11,  p. 
162,  1821. —  Gould,  Boston  Journ.  Nat.  Hist.,  iii,  p. 
400,  pi.  Ill,  fig,  10, 1840. — Binney,  Land  and  Fw,  Sh. 
N.  Am.,  I,  p.  241,  fig,  419,  1869, 

Range.  —  The  United  States  east  of  the  Rocky 
Mountains,  and  Canada. 

Red  Deer,  Alberta ;   Brandon,  Manitoba. 


Fig,  10.  Bifida- 
ria armifera 
(magnified). 


Fig.  II.  Bifid- 
aria  contracta 
(magnified). 


Bifidaria  contracta  Say. 

Pupa  contracta  Say,  Joum,  Acad,  Nat.  Sci.  Phila.,  11,  p, 
374,  1822, — Gould,  Boston  Joum.  Nat,  Hist,,  iii, 
p.  399,  pi.  Ill,  fig.  22,  1840. — Binney,  Land  and  Fw, 
Sh,  N,  Am,,  I,  p,  242,  figs.  420-422,  1869, 

Range.  —  Eastern   North    America   from    Mexico 
to  British  America,  east  of  the  Rocky  Mountains. 
Carberry,  Manitoba. 


28 


LAND    AND    FRKSH    WATER    MOLLUSKS 


Bifidaria  holzingeri  Sterki. 

Pupa  holzingeri  Sterki,  Nautilus,  m,  No.  4,  p.  37,  Aug.,  1889. — Binney, 

Bull.  Mus.  Comp.  Zool.,  xix.  No.  4,  p.  193,  fig.,  p.  194,  1890. 
Bifidaria  holzingeri  Pilsbry,  Class.  Cat.,  p.  19,   1898. 

Range.  —  Illinois  and  Kansas,  northward  to  British  America. 
Red  River  drift,  Brandon,  Manitoba ;  Red  Deer,  Alberta, 

Bifidaria  pentodon  Say. 

Veriigo pentodon  Say,  Journ.  Acad.  Nat.  Sci.  Phila.,  li,  p.  376,  1822. 
Pupa  pentodon  Gould,  Boston  Journ.  Nat.   Hist.,  iv,  p.  353,  pi.  xvi,  figs, 
lo-ii,  1843.  — Binney,  Land  and  Fw.  Sh.  N.  Am.,  i,  p.  236,  figs.  405- 
409,  1869. 


a  b  c 

Fig.  12.     Bifidaria  pentodon  (magnified),  showing  variations  in  aperture. 

Range.  —  Eastern  United  States  from  Texas  to  British  America ; 
southeastern  Nevada,  Quebec ;  Ontario ;  Manitoba  (rare)  ;  Alberta, 
at  Laggan. 

Genus  Pupilla  (Leach)  Turton. 

Pupilla  blandi  Morse. 

Pupilla  blandi  Morse,  Ann.  N.  Y.  Lye.  Nat.  Hist.,  viii, 

p.  211,  fig.  8,  1865. 
Pupa  blandi  Binney,  Land  and  Fw.  Sh.  N.  Am.,  i,  p.  235, 

fig.  402,  1869. 
f  Pupa  signata  Westerlund,  1885,  not  of  Mousson. 

Range. — Upper  Missouri,  Rocky  Mountains  ;  New 
Mexico  to  Colorado  ;   Canada ;  Red  Deer,  Alberta. 

Pupa  signata  was  described  from  the  Caucasus, 
and  its  inclusion  by  Westerlund  in  a  list  of  American 
Arctic  species  is  probably  an  oversight. 


Fig.  13.  Pu- 
pilla blandi 
(magnified). 


Pupilla  musconim  Linn6. 

Turbo  muscorum  Linn6,  Syst.  Nat.,ed,  x,  p.  y6j,  1758;  ed.  xii,  p.  1240, 
1767.  —  Hanley,  Shells  of  Linn.,  p.  352,  pi.  iv,  fig.  6,  1855. 

Pupa  muscorum  var.  bigranata  Rossmassler,  fide  Westerlund. 

Pupa  badia  Adams,  Boston  Journ.  Nat.  Hist.,  iii,  p.  331,  pi.  in,  fig.  18,  1840. 

Pupilla  badia  Morse,  Journ.  Portland  Soc.  N.  Hist.,  i,  p.  37,  figs.  89-91,  pi. 
X,  fig.  92,  1864. 

Pupa  muscorum  var.  lundstromi  Westerlund,  Ges.  Nat.  zu  Berlin,  p.  36, 
Mar.,  1883. 


FAMILY    PUPID^ 


29 


Pupa  {Pupilla)  muscorum  Pilsbry,  Nautilus,  xi,  p.  118,  Feb.,  1898. 
Pupa  sublubrica  Aucey,  fide  Binney. 

Range.  —  Europe.     In  America,  New  England  and  Canada  ;  Anti- 
costi ;    the  northern  United  States   as   far   west   as  Montana,  alpine 


H 


15 


16 


Figs.  14-16.  Pupilla  muscorum,  showing  variations.  Fig.  16  from  a  Euro- 
pean specimen.  Fig.  14  from  P.  badia  Adams.  Fig.  15  maximum  armature  of 
mouth.     (All  magnified.) 

(8,000-9,000  feet)  in  Colorado,  Utah  and  Nevada;    northward  in 
British  America. 

Laggan,  Alberta;  Anuk,  Alaska. 

Genus  Vertigo  Miiller. 
Vertigo  hoppii  Moller. 

Pupa  hoppi  Moller,  Ind.  Moll.  Gronl.,  p.  4,  1842.  — Pfeiffer,  Conch.  Cat, 

ed.  11,  Pupa,  p.   163,  pi.  XIX,  figs.   29,  30,  1852. — Tryon,  Ann.  Journ. 

Conch.,  Ill,  p.  303,  pi.  XV,  fig.  3,  1867. 
Fhipa  (^Vertigo)  hoppii  MoRCH,   Am.  Journ.   Conch.,   iv,  p.   30,  pi,  in,  figs. 

6-9,  1869. 
Pupa  steenbuchi  Beck,  Verz.   Kiel.,  p.  76,  1847  ;  nomen  nudum,  fide  Morch, 

op.  cit. 

Range.  —  Greenland  (Ungava,  Labrador.?). 

The  references  to  this  species  as  found  in  Alberta  and  Anticosti  are 
doubtless  based  on  a  different  species,  as  is  Binney 's  figure  on  page 
235  of  the  Land  and  Fresh  Water  Shells,  part  i. 

Vertigo  modesta  Say. 

Pupa  modesta  Say,  Rep.  Long's  Exp.,  11,  p.  259,  pi.  xv,  fig.  5,  1824. 
Pupa  decora  Gould,  Proc.  Boston  Soc.  Nat.  Hist.,  11,  p.  263,  fig.,  1848. 
Vertigo  parietalis  Ahcev  ;  P.  corpulenta  Morse,  and  V.  castanea  Sterki,  yf<ar<? 

Pilsbry,  Proc.  Acad.  Nat,  Sci.  Phila.,  for  1900,  pp.  597-602,  pi.  xxiii, 

figs.  1-7,  1900. 


30 


LAND    AND    FRESH    WATER    MOLLUSKS 


Range.  —  North  America  from  New  England  to  California  and 
northward.     Loess  of  Iowa. 

Ungava,  Labrador !  Lake  Superior  region ;  Laggan,  Alberta ;  in 
British  Columbia  at  Nanaimo  and  Victoria ;  in  Alaska  at  Killisnoo, 
Chilkat  and  Chilkoot  valleys,  Pyramid  Island,  Portage  Bay,  Dyea, 
Klukwan,  Point  Romanof  at  the  Yukon  delta ;  St.  George  Island ! 
St.  Paul  Island !  Unalaska !  Rooluk  Island,  Unalga  Pass !  Akutan 
Island  !  Popof  Island,  Shumagins  !  St.  Paul,  Kadiak  Island  !  Orca, 
Prince  William  Sound  !  Yakutat  Bay  !  Berg  Inlet,  Glacier  Bay  !  Muir 
Inlet ! 

This  is  the  most  abundant  and  widely  distributed  species  in 
the  north  country.  I  have  very  little  doubt  that  V.  borealis  More- 
let,  from  Kamchatka  and  Bering  Island,  is  merely  a  variety  of  this 
species. 

Vertigo  columbiana  Sterki. 

Vertigo  columbiana  (Sterki  MS.)  Pilsbry,  Proc.  Acad.  Nat.  Sci.  Phila.,  for 
1900,  p.  602,  pi.  XXIII,  fig.  II,  Sept.,  1900. 

Range.  —  Douglas  County,  Oregon,  and  northward  to  Washington, 
Vancouver  Island,  and  St.  Paul  Island,  Bering  Sea ! 

Resembles  V.  gouldii  but  wants  the  basal  fold.  A  variety  occurs  in 
Utah.     The  St.  Paul  specimen  was  identified  by  Dr.  Sterki. 

Vertigo  gouldii  Binney. 

Pupa  gouldii  Binney,  Proc.  Boston  Soc.  Nat.  Hist.,  i,  p.  105,  1843  ;  Terr. 
Moll.,  II,  p.  332,  pi.  Lxxi,  fig.  2,  185 1. 


a  b 

Fig.  17.    Fc^/«^o^o«/<f«  (magnified).   Fig.  18.    Verfi£'o  bollesiana  (magnified) . 

Vertigo  gouldii  MORSB,  Am.  Nat.,  i,  p.  669,  fig.  60,  1868. — Joum.  Portland 

Soc.  N.  Hist.,  I,  p.  38,  fig.  95,  pi.  X,  fig.  96,  1864. 
Vertigo  bollesiana  Morse,  Ann.  N.  Y.  Lye.  Nat.  Hist.,  viii,  p.  209.  figs.  4-6, 

1865. 


FAMILY    PUPID^ 


31 


Vertigo  bollesiana  var,  arthuri  von  Martens,  Sitz-ber.  Ges.  Naturf.  Fr.   zu 
Berlin,  1882,  No,  9,  p.  140. 

Range.  —  Northern  United  States  east  of  the  Rocky  Mountains  and 
northward. 

Ottawa,  Ontario ;  Manitoba ;  Upper  Missouri  at  Fort  Berthold ; 
Helena,  Montana. 

The  variety  arthuri  is  catalogued  from  Arctic  America  by  an  over- 
sight, in  Binncy's  Third  Supplement,  p.  185.  It  is  really  from  the 
Little  Missouri  in  Dakota. 

Vertigo  ventricosa  Morse. 

Isthmia  ventricosa  Morse,  Ann.  N.  Y.  Lye.  N.  Hist.,  viii,  p.  i,  figs.  1-3,  1865. 
Vertigo  ventricosa  Morse,  Am.  Nat.,  1,  p.  966, 

figs.  61,  62,  1868. 
Vertigo  ventricosa  elatior  Sterki,  Nautilus,  xi, 

p.  120,  Feb.,   1898. 
Vertigo   gouldii    lagganensis     Pilsbry,    Proc. 

Acad.   Nat.  Sci.   Phila  ,   for  1899,  p.    314, 

fig.  I. 
Vertigo  approximans  Sterki,  fide  Pilsbry. 

Range.  —  Quebec  and  Maine  to  Illinois 
and  Alberta ,  Manitoba ;  variety  elatior  at 
Laggan,  Alberta. 


a  b 

Fig.  19.      Vertigo  ventricosa 
(magnified). 


Vertigo  binneyana  Sterki. 

Vertigo  binneyana  Sterki,  Proc.  Acad.  Nat.  Sci.  Phila.,  for  1890,  p.  33  ; 
Nautilus,  III,  p.  125,  March,  1890.  —  Pilsbry,  Proc.  Acad.  Nat.  Sci. 
Phila.,  for  1899,  p.  315,  fig.  2  ;  Nautilus,  iv,  p.  39,  pi.  i,  fig.  I,  Aug., 
1890. 

Range.  —  Rocky  Mountain  region  from  Albuquerque,  New  Mexico, 
to  Manitoba. 

Seattle,  Wash. ;  Helena,  Montana ;  Winnipeg,  Manitoba. 


ao  21  22 

Figs.  20-22.     Vertigo  ovata,  showing  variations  in  teeth  (see  next  page). 


32 


LAND    AND    FRESH    WATER   MOL.LUSKS 


23a  23^  23c 

Fig.  23.  Vertigo  ovata,  showing  variations  in  teeth  of  aperture  (all  figures 
magnified). 

Vertigo  ovata  Say. 

Vertigo  ovata  Say,  Journ.  Acad.  Nat.  Sci.  Phila.,  11,  p.  375,  1822.  —  Morse, 
Am.  Nat.,  i,  p.  668,  figs,  57,  58,  1868.  — Binney,  Land  and  Fw.  Sh.  N. 
Am.,  I,  p.  252,  figs.  442-445,  1869  (syn.  in  part  excl.). 

Range.  —  Eastern  United  States  from  Maine  to  Texas,  and  north- 
ward.    Mexico.? 

Ungava  Bay,  Labrador!  Victoria,  British  Columbia!  St.  Paul, 
Kadiak  Island !  Alaska ;  Tigalda  Island,  Aleutian  chain !  Laggan, 
Alberta ;  Manitoba. 

Vertigo  arctica  Wallenberg. 

Pupa  arctica  Wallenberg,  Mai.  Blatt,  v,  pp.  32,  99,  pi.  i,  figs.  3,  a-c,  4, 
1858.  —  Reinhardt,  Sitz-ber.  Ges.  Naturf.  Fr.  zu  Berlin,  No.  3,  1883, 
p.  38. 

Range.  —  Lapland  and   northern  Scandinavia,  the  mountains   of 

Germany  and  the  Tyrol ;   eastern  Siberia  at  Emma  Harbor,  Plover 

Bay ;  Port  Clarence  on   the  American  side  of  Bering  Strait  (Vega 

Expd.) . 

*  Vertigo  krauseana  Reinhardt. 

Vertigo  krauseana  Reinhardt,  Sitz-ber.  Ges.  Naturf.  Fr.  zu  Berlin,  No.  3, 
1883,  p.  38.  —  Westerlund,  Fauna  Pal.  Reg.,  iii,  p.  131,  1887. 

Range.  —  Chukchi  Peninsula  of  eastern  Siberia;  at  Poot,  St.  Law- 
rence Bay,  and  Ratmanof  Harbor.     Alaska,  at  Chilkat  Inlet ! 

Specimens  of  this  species  labeled  Chilkat  Inlet  were  received  from 
Dr.  Krause ;  but  in  the  publications  on  this  form  only  the  Siberian 
habitats  are  given.  I  suspect  some  error  has  occurred  in  labeling, 
though  it  is  entirely  possible  that  the  species  may  occur  in  Arctic 
America. 

♦Vertigo  (Vertilla)  milium  Gould. 

Pupa  milium  GovLT),  Boston  Journ.  Nat.  Hist.,  ill,  p.  402,  pi.  Ill,  fig.  23,  1840. 
Vertigo  {Angustula)  milium  Sterki,  Proc.  U.  S.  Nat.  Mus.,  XI,  pp.   377-S, 
pi.  XLii,  figs.  10,  13,  1888. 


FAMILY   ACHATINID^  33 

Vertigo {Vertilla)mtlium  Pilsbry,  Proc.  Acad.  Nat.  Sci.  Phila.,  £011900,  p.  597. 

Range.  —  New  England  to  Texas  and  Florida, 
west  to  Minnesota.     Ontario,  Canada. 

This  minute  species  doubtless  exists  on  the  northern 
side  of  the  boundary,  though  not  yet  reported 
there.  Fig.  24.  Verti- 

go milium  (mag- 

*  Vertigo  (Isthmia)  pygmaea  Draparnaud.  nified). 

Pupa pygmaa  Draparnaud,  Tableau,  p.  57,  1801  ;  Hist.  Moll.  Terr,,  p.  60, 

pi.  Ill,  figs.  20-21,  1805. 
Vertigo pygmcea  Pilsbry,  Proc.  Acad.  Nat.  Sci.  Phila.,  for  1900,  p.  608. 
Vertigo  callosa  Sterki,  not  Reuss,  and  P.  superioris  Pilsbry,  fide  Pilsbry,  1.  c. 

Range.  —  Europe,  Asia  Minor,  the  Caucasus ;  America,  in  the 
northeastern  States  and  the  Lake  Superior  region. 

Family  ACHATINIDJE. 

Genus  Cochlicopa  (F^russac)  Risso. 

Cochlicopa  lubrica  Muller. 

Helix  lubrica  Muller,  Verm.  Hist.,  i,  p.  104,  1774. 

Zua  lubrica  Leach,   Syn.    Moll.   Gt.   Brit.,   p.   114,    1852  ^  Gray's  Turton's 

Man.,  p.  188,  pi.  VI,  fig.  65,  1840. 
Cionella  lubrica  Jeffreys,  Trans.   Linn.  Soc,  xvi,  p.  347,  1830.  — Binney, 

Land  and  Fw.  Sh.  N.  Am.,  i,  p.  224,  figs.  381-385. 
Bulimus  lubricoides  Stimpson,  Shells  of  New  England,  p.  54,  1851. 
Zua  lubricoidea  Morse,  Jour.  Portland  Soc.  Nat.   Hist.,  i,  p.  30,  figs.  79,  81, 

84  ;  pi.  X,  fig.  82,  1864  ;  Am.  Nat.,  i,'p.  607,  fig.  49,  1868. 
Ferussacia  subcylindrica  auct.  non  L. 

Range.  —  Europe,  North  Africa  and  Asia  Minor :  Siberia  ;  Kam- 
chatka ;  most  of  North  America. 

Lake  Superior  region ;  Red  River  of  the  North,  Lake  of  the  Woods 
and  Turtle  Mountain,  Manitoba ;  Moose  Factory !  English  River, 
Keewatin  ;  Laggan  and  Red  Deer  in  Alberta ;  Nanaimo  and  Victoria, 
British  Columbia ;  Point  Barrow  !  and  Yukon  valley,  Alaska  ;  Avacha 
Bay  !  Kamchatka. 

This  well  known  shell  is  one  of  the  most  emphatically  circumpolar 
species  in  existence,  and  considering  its  immense  geographical  and 
climatic  range  its  resistance  to  the  factors  which  make  for  variation  is 
very  remarkable. 

Family  CIRCINARIID^. 
Genus  Circinaria  Beck. 

This  is  Macrocyclis  or  Selenites  of  recent  literature,  not  of  Beck 
or  Hope. 


34  LAND    AND    FRESH    WATER    MOLLUSKS 

Circinaria  vancouverensis  Lea. 

Helix  vancouverensis  Lea,  Trans.  Am.   Phil.  Soc,  vi,  p.  87,  pi.   xxill,  fig. 

72,  1839. 
Helix  vellicata  Forbes,  Proc.  Zool.  Soc.  London,  1850,  p.  75,  pi.  ix,  fig.  i. 
Macrocyclis  vancouverensis  Tkyou,  Am.  Joum.  Conch.,  11,  p.  245,  pi.  m,  fig. 

6,  1866.  — BiNNEY,  Land  and  Fw.  Sh.  N.  Am.,  i,  p.  54,  figs.  90-93,  1869. 
Selenites  vancouverensis  Binney,  Third  Suppl.  Terr.  Moll.  pp.  163-6,  1892. 
Circinaria  vancouverensis  Pilsbry,  Class.  Cat.  Am.  Landsh.,  p.   24,  1898. 

Range.  —  In  the  moist  and  wooded  region  of  northern  California 
and  northward  to  the  Alexander  Archipelago,  Alaska,  between  the 
Cascade  Range  and  the  sea. 

Vancouver  Island !  Quatsino  Sound,  Broughton  Strait,  Malcolm 
Island,  Johnstone  Strait,  Harbledown  and  Pender  Islands,  Skidegate, 
Graham  Island,  and  Cumshewa  Inlet,  Moresby  Island,  Queen  Char- 
lotte Islands  !  Union  Bay  !  and  Comox  !  British  Columbia.  In  Alaska 
at  Annette  Island  !  Killisnoo,  Sitka  !  Lynn  Canal,  throughout  the  Alex- 
ander Archipelago,  and  northward  along  the  mainland  shore  to  Lituya 
Bay. 

The  typical  form  of  this  species  is  readily  recognizable  by  its  ample 
whorls,  the  last  nearly  smooth,  its  large  size  and  greenish  yellow  color. 
It  grades,  however  imperceptibly,  into  the  smaller  and  more  strongly 
sculptured  C.  sfortella  Gould,  from  which  cause  a  large  number  of 
varieties  have  arisen  and  been  named.  In  the  moist  mountainous 
region  of  the  Columbia  drainage  some  of  these  forms  penetrate  to  the 
eastward  nearly  to  the  headwaters  of  this  river  in  western  Montana. 
They  are  all  depauperate,  however,  compared  with  the  typical  well 
nourished  forms  of  the  coast.  These  animals  are  carnivorous,  voracious 
and  cannibalistic.  It  is  unsafe  to  keep  them  living  in  the  same  recep- 
tacle with  other  living  snails,  as  they  will  rapidly  destroy  and  consume 
the  soft  parts. 

A  fine  sinistral  specimen  was  collected  at  Sitka. 

A  variety  of  a  dark  chocolate  brown  color,  otherwise  like  the  ordi- 
nary form,  was  found  rather  commonly  at  Sitka.  For  this  the  varietal 
name  chocolata  would  seem  appropriate. 

Specimens  of  this  species  were  received  with  a  label  indicating  that 
they  had  been  collected  on  the  Alaska  Peninsula  opposite  Kadiak 
Island,  but,  knowing  the  habits  of  this  animal,  I  regard  this  as  an 
error  of  labelling.  The  collector  having  died,  I  was  unable  to  untangle 
the  confusion,  but  I  have  never  found  it  far  distant  from  the  wooded 
region  where  Ariolimax  and  Polygyra  Columbiana  occur,  upon  which 
it  chiefly  feeds  in  Alaska.  It  does  not  occur,  so  far  as  I  was  able  to 
discover,  on  the  shores  of  Cook  Inlet,  where  there  are  suitable  forests, 


FAMILY    ZONITID^  35 

and  I  do  not  believe  it  occurs  on  the  treeless  grassy  slopes  of  the 
peninsula.  I  suspect  that  the  wide-stretching  glacial  area  to  the 
north  and  west  of  Yakutat  Bay,  puts  an  impassable  barrier  to  its  north- 
western migration,  and  that  it  may  not  exist  in  the  forests  beyond  that 
area. 

This  is  the  largest  shell-bearing  Pulmonate  known  to  live  in  Alaska, 
but  is  surpassed  by  the  great  slug  Ariolimax^  which  often  extends  to 
the  length  while  preserving  the  diameter  of  a  large  cigar. 

Circinaria  variety  sportella  Gould. 

Helix  sportellaQovXA,  Proc.    Boston  Sec.  Nat.   Hist.,  ii,  p.  167,  1846;  Moll. 
U.  S.  Expl.  Exp.,  p.  37,  fig.  42,  1852. 

This  is  a  variety  of  C.  vancouverensis  of  smaller  size,  and  intensified 
sculpture,  both  spiral  and  incremental.  Intermediate  forms,  to  which 
several  names  have  been  applied,  connect  it  with  the  typical  form.  It 
accompanies  the  latter  throughout  its  range,  but  occurs  in  some  locali- 
ties which  do  not  support  the  larger  form.  Among  northern  localities 
it  has  been  collected  at  Saanich,  Comox  !  Union  Bay  !  Salt  Springs 
Island  and  Chilliwak  Lake,  British  Columbia  ;  at  Annette  Island  !  (with 
variety  hybrida  Ancey)  and  Lituya  Bay  !  Alaska. 

Circinaria  variety  hybrida  Ancey,  1888. 

This  form  is  reported  from  Vernon  and  Comox,  British  Columbia, 
and  Annette  Island,  Alaska. 

Circinaria  heniphilli  Binney  and  C.  voyana  Newcomb,  have  not 
been  authentically  reported  north  of  the  boundary,  though  it  is  said 
both  of  them  have  been  collected  in  the  Puget  Sound  region. 

Family  ZONITIDiE. 
Genus  Vitrina  Draparnaud. 

Vitrina  Draparnaud,  Tabl.  Moll.  Terr.  France,  pp.  33,  98,  1801  ;  Hist.,  Nat. 

Moll.  Terr.  France,  pp.  23,  30,  119,  1805.    Type  Helix  pellticida  Muller, 

Verm.  Terr.,  p.  215. 
Vitrinus  Montfort,  Conch.  Syst.,  11,  p.  238,  18 10. 
Cobresia  Jac.   Hubner,   Mon.  Test.  Bairische  Landschn.  Cobresien,  1810  ; 

(pages  and  plates  not  numbered). 
Hyalina  Studer,    Syst.    Verz.   Schweiz.  Conch.,  p.    11,  1820:  not  of  Schu- 
macher, 1817. 
Limacina  Hartmann,  Neue  Alpina,  i,  p.  206,  1821  ;  Sturm's  Deutschl.  Fauna, 

abth.  VI,  heft  V,  pp.  41,  54,  1821  ;  not  of  Cuvier,  1817. 
Helicolimax  F^russac  pere,  Mem.  Soc.  Med.  d'EmuL,  iv,  p.   390,  1802  ;    et 

fils,  Tabl.  Syst.  des  Lim.,  pp.  19,  21,  1821. 
Semilimax  Ferussac  pere,  Der  Naturforscher  (Halle),  pt.  28,  1802,  fide  Fer- 

russac  fils,  loc.  cit.,  1821. 


36  LAND    AND    FRESH    WATER    MOLLUSKS 

Semilimax  Stabile,  Revue  et  Mag.  Zool.  (Guerin),  Aug.,  1859,  p.  41  ;  Moll. 

Terr.  Viv.  Piem.,  p.  23,  1864. — Kobelt,  Cat.  der  Europ.  Faun.  leb.  Bin- 

nenconch.,  p.   3,  1871  (as  a   section  of  Vitrina,  group  of  V.  diaphana 

Drap.).  — Pfeiffer,  Nom.  Hel.  Viv.,  p.  26,  1878. 
Pagana  Gistel,  Naturg.  Thierr.,  p.  168,  1848  (new  name  for  Vitrina  Drap.). 
Phenacolimax  Stabile,  R6v.  et  Mag.  Zool.  (Guerin),  Aug.,  1859,  p.  42  ;  Moll., 

Terr.  Viv.  R6m.,p.  24,  1864. —  Pfeiffer,  Nom.  Hel.  Viv.,  p.  27,  1878. 
Helicolimax  Kobelt,  Cat.  der  Europ.  Faun.  leb.  Binnenconch. ,  p.  4,  1871, 

(Sect,  of  Vitrina,  s.s.). 
Trochovitrina  Schacko,  in  Boettger,  Jahrb.  Deutsch.  Mai.  Ges.,  vii,  p.   379, 

Oct.,  1880;  type  Vitrina  lederi^oQtiger . 
Gallandia  Bourguignat,  Descr.  Nouv.  Genre  Gallandia,  Aug.,  1880,  pp.  4-8, 

1st  sp.   Vitrina  conoidea  Martens. 
Oligolimax  Fischer,  in  Paulucci,  Faun.  Calabria,  p.  37,    1880.  —  Paulucci, 

Bull.  Soc.  Mai.  Ital.,  vii,  p.  75,  1881.  —  Fischer,  Man.  de  Conchyl., 

p.  464,  1883  {V.  pauluccicB  Fischer). 
Partnacellina  Sandberger,   Land  u.  Sussw.  Conch,  d.  Vorwelt,  p.   232,  pi. 

XIII,  1 87 1.     Sole  ex.  P.  vitrinaformis  Sandb.,  Eocene. 
Vitrina  Pilsbry,  Class.  Cat.  Landsh.  Am.,  p.  25,  1898. 
Chlamydea  Westerlund,   Fauna  d.   Pal.  Reg.,   i,  p.    19,   1886  ( F.    hicolor 

Westerlund,  1881). 

The  shell  in  this  group  and  its  allies  is  reduced  to  very  simple  terms 
and  the  differences  between  species  appear  trifling.  But  there  appears 
to  be  quite  a  wide  range  of  character  in  the  soft  parts,  from  whence 
it  follows  that  several  sections  can  be  recognized  in  the  genus  as  re- 
stricted, while  some  species,  formerly  regarded  as  belonging  to  Vitrina,^ 
are  now  scattered  in  widely  separated  genera. 

The  true  Vitrina  seems  confined  to  the  northern  hemisphere. 
The  following  sections  are  recognized  : 

Vitrina  Drap.  s.  s.  1801.  Type  V.  pellucida  Miiller.  Helicoli- 
max Ferussac  pere,  1801,  is  identical,  and  Semilimax  Stabile  hardly 
separable. 

Oligolimax  Fischer.     Type  V.  pauluccice  Fischer. 

Phenacolimax  Stabile,  1859.     Type   V.  major  F6r. 

Gallandia  Bourguignat,  Aug.,  1880.  Type  V.  conoidea  von 
Martens.      Trochovitrina  Schacko,  Oct.,  1880,  is  synonymous. 

The  North  American  and  Greenland  species  are  true  Vitrina^  the 
other  forms  belong  to  the  Old  World  only. 

The  New  World  groups  Vitrinozonites  Binney  and  Velifera  Binney 
may  be  regarded  as  of  generic  rank,  and  are  extra  limital  to  the  region 
now  under  discussion. 

Vitrina  angelicas  Beck. 

Vitrina  angelica  Beck,  Index,  p.  i,  1837  ;  name  only.— Moller,  Index,  p.  4, 
1842. — Morch,  Am.  Journ.  Conch.,  iv,  p.  27,  pi.  in,  figs,  i,  4,  1868.  — 
MoRCH,  in  Rink's  Danish  Greenland,  p.  436,  1877. 

Helix  pellucida  Fabricius,  Fauna  Gronl,,  p.  389,  1780,  not  of  Miiller,  1774. 


FAMILY    ZONITID^  37 

Range.  —  Greenland. 

This  species  is  more  like  the  V.  beryllina  of  Europe  than  the 
American  species.  The  latest  data  given  by  Posselt 
indicate  that  it  is  not  found  in  Iceland.  Binney  has 
given  an  enlarged  illustration  of  this  species  (fig.  25) 
in  his  Land  and  Fresh  Water  Shells  of  North  America,  fig.  25.  Vit- 
I,  p.  28.  rina  angelica,  \. 

Vitrina  limpida  Gould. 

Vitrina  pellucida  De  Kay,  Zool.  N.  Y.  Moll.,  p.  25,  pi.  ill,  fig.  42,  1843; 

not  of  Miiller,  1 774. 
Viirina  limpida  GovLQ,  in  Agassiz,  Lake  Superior,  p.   243,  1850. — Morse, 

Journ.   Portland  Soc.  Nat.  His.,  i,  p.  11,  pi.  v,  fig.  17,  1864.  —  Binney, 

Land  and  Fw.  Sh.  N.  Am.,  i,  p.  27,  figs.  23,  24,  1869. 
Vitrina  americana   Pfeiffer,    Proc.    Zool.    Soc.    Lond.,   for   1852,   p.  156; 

Conch.  Cab.,  ed.  11,   Vitrina,  p.  9,  pi.  i,  figs.  22-25,  1854. 

^_^  Range. —  Central  New^  York  and  northvsrard,  from 

'T^  W^^  ^^'^  Brunswick  to  Alberta  and  Hudson  Bay. 

^ — -^  Pittsburgh,  Pennsylvania.     Manitoba  at  Carberry 

Fig.  26.     Vit-  and  Lake  of  the  Woods ;  Red  Deer  and  Laggan  in 

rina       limpida  ^i^erta  ;  Moose  Factory  !  James  Bay ;  Norway  House, 

Maine),!.  •     a                   A 
m  damp  woods. 

This  species  has  been  reported  from  the  Rocky  Mountain  region  by 
Ingersoll,  but  I  regard  his  specimens  so  identified  as  varieties  of  V. 
alaskana. 

Vitrina  alaskana  Dall,  nom.  nov. 

Vitrina  pfeifferi  Newcomb,  Proc.  Cal.  Acad.  Sci.,  11,  p.  92,  1861. — Tryon, 
Am.  Journ.  Conch.,  11,  p.  244,  pi.  iii,  fig.  3,  1866.  —  Binney,  Land  and 
Fw.  Sh.  N,  Am.,  i,  p.  28,  fig.  26,  1869.  Not  V.  pfeifferi  Deshayes,  in 
F6r.,  Lima9ons,  1822. 

Range.  —  New  Mexico,  Utah,  Colorado,  central  California,  all  at 
considerable  altitudes,  and  northward. 

Nanaimo,  Vancouver  Island,  B.  C. ;  Muir  Inlet,  Alaska  !  St.  Paul, 
Kadiak  Island !  Popof  and  Unga  Islands,  of  the  Shumagin  group ! 
Akutan  !  Unalga  !  Rooluk  !  and  Unalaska  !  of  the  Aleutian  chain ;  St. 
Paul !  and  St.  George  Islands,  Bering  Sea,  Alaska,  in  tall  grass  of 
bluff  fifty  feet  above  the  sea  ! 

This  species  has  been  referred  to  as  pellucida .^  limpida  and  exilis^ 
and  when  fully  grown  under  favorable  conditions  the  shell  may  reach 
10  mm.  in  major  diameter,  though  most  of  the  specimens  as  collected 
are  considerably  smaller.  The  shell  is  translucent,  with  a  marked 
greenish  tinge,  and  not  over  three  whorls.     It  is  flatter  than  limpida^ 


38  LAND    AND    FRESH    WATER    MOLLUSKS 

larger,  and  of  a  different  tint,  and  the  size  of  the  whorls  increases 
more  rapidly.  It  is  less  flat  and  much  larger  than  V.  exi'h's,  which  is 
also  of  a  different  hue. 

It  is  the  most  common  land  shell  on  most  of  the  islands  of  Bering 
Sea  and  on  the  continent  near  the  sea,  where  it  usually  occurs,  but  as 
we  move  southward  we  find  it  occurring  at  continually  greater  eleva- 
tions and  entirely  absent  from  the  warm  dry  plains  and  valleys.  It 
attains  from  7,500  to  10,800  feet  elevation  in  the  Sierra  and  Rocky 
Mountains. 

*Vitrina  ezilis  Morelet. 

Vitrina  exilis  Morelet,  Journ.  de  Conchyl.,  vii,  p.  8,  1858. —  Pfeiffer, 
Mon.  Hel.  Viv.,  iv,  p.  799,  1859.  — Binney,  Bull.  U.  S.  N.  Mus.,  No. 
28,  p.  178,  fig.  172,  1885  ;  Terr.  Moll.,  v,  pp.  138,  200,  pi.  11,  fig.  B. 

Range.  —  Northeastern  Asia  and  adjacent  islands,  from  Japan 
northeastward. 

Kamchatka,  at  Petropavlovsk  !  Bering  Id.  (Vega  Expd.). 

This  is  a  small  species,  of  a  whitish  or  translucent  glassy  hue ; 
smaller  and  with  a  more  elevated  spire  than  its  American  representa- 
tive V.  alaskana.  According  to  Binney  V.  exilis  has  the  jaw  and 
radula  as  usual  in  the  genus,  the  transverse  rows  of  teeth  numbering 
37  •  ^  '375  with  seven  perfect  laterals. 

I  have  seen  no  specimens  from  east  of  the  Commander  Islands  ;  the 
shells  thus  identified  are  probably  all  V.  alaskana. 

Genus  Vitrea  Fitzinger. 
Vitrea  radiatula  Alder. 

Helix  radiatula  Alder,  Cat.  Test.  Newcastle  upon  Tyne,  p.  12,  No.  50, 
1830.  —  Gray,  in  Turton's  Man.,  p.  173,  pi.  xii,  fig.  137,  1840. 

f  Helix  hammonis  Strom,  Trondj.,  Selsk.  Skrift.,  p.  435,  pi.  vi,  fig.  16,  1765. 

?  Zonites  viridulus  Menke,  Syn.,  ed.  11,  p.  137,  1830. 

Helix  electrina  Govi^Vi,  Inv.  Mass.,  p.  183,  fig.  m,  1841. 

Hyalina  viridula  Binney,  Land  and  Fw,  Sh.  N.  Am.,  i,  p.  34,  figs.  41-43, 
1869  ;  not  of  Menke? 

Hyalina  pellucida  Lehnert,  Science  Record,  11,  p.  172,  June  16,  1884. 

Range. — Holarctic.     Northern  Europe,  Asia  and  America. 

Manitoba,  at  Lake  of  the  Woods,  Carberry  and  Pembina ;  Alberta, 
at  Laggan  and  Red  Deer ;  Fort  Resolution,  Great  Slave  Lake  !  British 
Columbia,  at  Departure  Bay !  Comox !  and  Union  Bay  !  Alaska,  at 
Killisnoo  !  Klukwan !  Portage  Bay  !  Seduction  Tongue  !  Anuk  !  St. 
Paul,  Kadiak  Island !  Unga  Island,  Shumagins  !  Unalaska,  Aleutians  ! 
Nulato,  Yukon  River!  Point  Barrow!  Bering  Island,  Bering  Sea! 
Petropavlovsk,  Kamchatka  ! 


FAMILY    ZONITID^  39 

The  species  as  described  by  Strom  is  unrecognizable  and  his  name 
should  be  rejected.  There  is  some  doubt  as  to  whether  the  Z. 
viridula  of  Menke  is  identical  with  the  present  species  or  not. 

Vitrea  nitidula  Drapamaud. 

Helix  nitidula  Draparnaud,  Hist.  Moll.,  p.  117,  pi.  viii,  figs.  21-22,  1805. 
Zonites  nitidulus  Gray,  in  Turton,  Man.,  p.  172,  pi.  xil,  fig.  136,  1840. 

Range.  —  Europe,  northern  and  middle  ;   Italy. 
Fort  Resolution!  Great  Slave  Lake  (Kennicott). 
The  identification  and  locality  are  indubitable. 

Vitrea  binneyana  Morse. 

Hyalina  binneyana  Morse,  Joum.  Portland  Soc.  Nat.  Hist.,  i,  p.  13,  figs.  25, 
26,  pi.  II,  fig.  9,  pi.  IV,  fig.   31,  1864.  — BiNNEY,  Land  and  F\v.  Sh.  N. 
Am.,  I,  p.  39,  figs.  56-8,  1869. 
Helix  morsei  Tkyou,  Am.   Joum.   Conch.,  i,  p.   188, 

1865. 
Hyalina  dinneyi  BmtiEY,  Land  and  Fw.  Sh.  N.  Am., 

I,  p.  39,  footnote. 
Vitrea  binneyana  Pilsbry,  Class.  Cat.,  p.  26,  1898. 
Fig.  27.     Vitrea  bin-  ^      ,  ,-»*-•  1  ■»  ^r.  . 

neyana  Morse  Range. — Quebec  and  Maine  to  northern  Mich- 

igan and  British  Columbia. 
Brandon,  Manitoba ;  Nanaimo,  B.  C. 

Vitrea  indentata  Say. 

Helix  indentata  Say,   Joum.   Acad.    Nat.   Sci.    Phila.,    11,  p.  372,    1822. — 

Gould,  Inv.  Mass.,  p.  181,  fig.  109,  1841. 
Hyalina  indentata  Morse,  Joum.   Portland  Soc.  Nat.  Hist.,  i,  p.  12,  fig.  21; 

pi.  II,  fig.  II,  pi.  V,  fig.  22,  1864.  —  Binney,  Land  and  Fw.  Sh.  N.  Am., 

I.  P-  35.  figs-  44-46,  1869. 
Range.  — Mexico  to  Manitoba,  United  States  and  Canada,  eastward 
from  the  Rocky  Mountains.     Pine  Creek,  Manitoba. 

Genus  Euconulus  Reinhardt. 

Helix  (sp.)  Muller,  Gmelin,  Montagu,  Drapamaud,  etal.,  1774- 1820. 
Trochus  (sp.)  Da  Costa,  Brit.  Conch.,  p.  35,  1778. 

Teba  (sp.)  Leach,  Proofsheets,  1820,  fide  Rossmassler  Icon. ,  11,  p.  38,  1838. 
Conulus  FiTZiNGER,   Syst.   Verz.  Weichth.,   p.  94,  1833  ;  not  Conulus  Rafi- 

nesque,  Analyse  de  la  Nature,  p.  145,  181 5. 
Polita  (sp.)  Held,  Weichth.  Bayems,  Isis,  Dec,  1837,  col.  916. 
Petasia  (sp.)  Beck,  Index,  p.  21,  1837. 

Zonites  (sp.)  Moquin  Tandon,  Moll,  de  France,  p.  68,  1855. 
Hyalina  (sp.)  von  Martens'  Albers,  p.   73,  1850.  —  Binney,  L.  &  Fw.  Sh. 

N.  Am.,  pt.  I,  p.  46,  1869. 
Euconulus  (J'ulvus)  Reinhardt,  Sitzb.  Ges.  Naturf.  Fr.  zu  Berlin,  for  1883, 

p.   86.  —  PiLSBRY,    Nautilus,    xiv,    Nov.,  1900,   p.    81. — Woodward, 

Brit.  Nonmarine  Moll.,  p.  353,  1903. 
Hyalinia  (sp.)  Morch,  Syn.  Moll.  Terr.  Dan.,  p.  14,  1864. — Westerlund, 

Nachrichtsbl.  Mai.  Ges.,  xv,  p.  173,  Dec.,  1883. 


40  LAND    AND    FRESH   WATER    MOLLUSKS 

Arnouldia  Bourguignat,  Bull.  Soc.  Mai.  de  France,  vii,  p.  328,  1890. 
Vitrea  (sp.)  E.  A.  Smith,  Journ.  Conch.  (Leeds),  vi,  p.  339,  1891. 
Trochulus  Westerlund,   Fauna  Pal.  Reg.,  iii'*beil,  p.  16,  1886  ;  not  of  the 

Museum  Calonnianum,  p.  26,  1797,  not  Trochula  Schleuter,  Verz.,  p.  7, 

1838. 

This  genus  has  had  a  number  of  names  applied  to  it,  among  which 
one  is  proposed  by  Westerlund  as  taken  from  Da  Costa  (1778)  but,  as 
indicated  by  Sherborne  in  the  Index  Animaliutn^  Da  Costa  merely 
quoted  part  of  a  polynomial  phrase  (^Trochilus  terrestris  jnortoni) 
in  his  synonymy,  from  Morton's  Northamptonshire  (London,  171 2), 
and  did  not  use  the  word  Trockilus  in  a  generic  sense.  Moreover,  if 
he  had,  Trockilus  had  previously  been  used  by  Linn^  for  a  genus  of 
birds.  There  seems  at  present  no  reason  to  doubt  that  the  first  valid 
name  for  the  genus  is  Euconulus  Reinhardt,  while  the  typical  species, 
as  will  be  evident  from  the  following  synonymy,  is  E.  trochiformis 
(Montagu) . 

Euconulus  trochiformis  (Montagu). 

?  Helix  fulva,  ex  parte  Muller,  Verm.  Terr,  et  Fluv.,  11,  p.  57,  1774  ;  Zool. 

Dan.  Prodr.,  p.  240,  No.  2905,  1776. 
Trochus  terrestris  (Lister)  Da  Costa,   Brit.   Conch.,  p.   35,    1778  ;  not   of 

Pennant,  1767. 
Helix  trochiformis  Montagu,  Test.  Brit.,  11,  p.  427,  pi.  11,  fig.  9,  1803.     Not 

of  Ferussac,  1819. 
Helix  trochulus  Montagu,  op.  cit.,  in  syn.,  not  of  Muller,  1774.  —  Dillwyn, 

Descr.  Cat.  Rec.  Sh.,  11,  916,  181 7. 
Helix  fulva  Draparnaud,  Hist.  Nat.  des  Moll.  Ten  et  Fluv.  France,  p.   81, 

pi,  VII,  figs.  12,  13,  1805. — RossMASSLER,  Icon.,  II,  pt.  II,  p.  38,  pi.  39, 

fig.  535,  1838. 
Helix  nitidula  von  Alten,  Syst.  abh.  Erd.  u.  Fluss-Conch.,  p.  53,  pi.  iv,  fig. 

8,  1812. 
Helix  fulva  Nilsson,  Hist.  Moll.  Suec,  p.  13,  1822. 
Helix  trochiformis  Maton  and  Rackett,  Linn.  Trans.,  viii,  p.  200,  1807. — 

Fleming,  Edin.  Encyc,  vii,  p.  80,  18 13. — Wood,  Ind.  Test.,  pi.  32,  fig. 

68,  1825. — Jeffreys,  Linn.  Trans.,  xvi,  p.  331,  1830. 
Teba  fulva  Leach,  Syn.  Brit.  MolL  Proofsheets,  p.  99,  1Z20  \  fide  Rossmas- 

sler.  Icon.,  11,  p.  38,   1838. — Leach,  Syn.  Brit.  MolL  (ed.  Gray),  p.  72, 

1852. 
Helix  trochilus  Fleming,  Brit.  An.,  p.  260,  1828. 

Helix  mandralisci  Bivona,  Nuovo  Moll.  Palermo,  p.  16,  pi.  i,  fig.  6,  1839. 
Helix  fulva  vzx.  mortoni  Jeffreys,  Linn.  Trans.,  xvi,  p.  332,  1830. 
Conulus fulvus  Fitzinger,  Syst.  Verz.,  p.  94,  1833. 
Polita  fulva  Held,  Weichth.  Bayerns,  Isis,  Dec,  1837,  col.  916. 
Helix  {Petasia)  trochiformis  Beck,  Index,  p.  21,  1837. 
Zonites  {Conulus)  fulvus  MoQ.  Tandon,  Moll.  France,  p.  68,  1855. 
Helix  {Conulus)  fulva  Alweks,  Heliceen,  p.  73,  1850. 
Hyalina  {Conulus)  fulva  voN  Martens'  Albers,  p.  73,  i860. 
Hyalinia   {Petasia)  fulva  Morch,  Syn.  Moll.  Terr.  Dan.,  p.  14.  1864. 
Euconulus  fulvus  Reinhardt,  Sitzb.  Ges.  Naturf.  Freunde  zu  Berlin,  p.  86, 

1883. 


FAMILY    ZONITID^  4I 

Arnouldia  fulva  Bourguignat,  Bull.  Soc.  Mai.  de  France.,  vii,  p.  328,  1890. 
Vitrea  {Conulus)  fulva  E.  A.  Smith,  Journ.  Conch.  (Leeds),  vi,  No.  x,  p.  339, 

1891. 
£uconu/us/u/vus  Woodward,  Brit.  Nonmarine  Moll.,  p.  353,  1903. 
//e/tx  egena  Say,  Journ.  Acad.  Nat.  Sci.  Phila.,  v,  p.  120,  1825. 
Hyalina  (^Conulus)  fulva  Binney,  Land  and  Freshw.  Sh.  of  N.  Am.  part  i,  p. 

46,  fig.  73.  1869. 
Hyalinia  {Conulus)  trochifortnis  (Montagu)  Westerlund,  Nachr.  Mai.  Ges., 

XV,  p.  173,  Dec,  1883. 
Trochulus  trochifortnis  Westerlund,  Fauna  Pal.  Reg.,  iii'*  beilage,  p.  16, 

1886. 
Conulus  chersinus  Morse,  Journ.  Portland  Soc.  N.  Hist.,  i,  p.  19,  figs.  44, 

46,  pi.  II,  fig.  4,  pi.  VII,  fig.  45,  1864,  not  Helix  chersina  Say,  1821. 
Conulus  fulvus  (MiJLLER),  and  var.  alaskensis  Pilsbry,   Nautilus,  xil,  No. 

10,  pp.  1 1 5-6,  1899. 
Euconulus  fulvus  ViuSBKY ,  Nautilus,  xiv,  Nov.,  1900,  p.  8i. 

YdLntiy  fabricii  (Beck). 

Helix  nitida  Fabricius,  Fauna  Gronl.,  p.  389,  1780,  not  of  MuUer. 
Helix  {Petasia)  fabricii  Beck,   Index,  p.   21,    1837,  nude  name. — Moller, 
Index  Moll.  Grcenl.,  p.  7,  1842. 

Range.  —  Holarctic,  and  widely  distributed  south- 
ward. 

Canada ;  Manitoba  at  Carberry,  Pine  Creek,  Pem- 
bina, and  Lake  of  the  Woods  ;  in  Alberta  at  Laggan,         © 
Red  Deer,  Olds  and  McLeod ;  English  River,  Kee-       ^^g-  ^S.    Eu- 

watin ;   California !   Oregon !  Washington !  Victoria,      ,"     .    ,         "" 
00  1     formts    (magni- 

Vancouver  Island  !  Sitka,  Alaska ;  Unalaska  !   Bering    ^^^\ 

Island,  Bering  Sea  !  Petropavlovsk,  Kamchatka  ! 

Pooten,  Konyam  and  St.  Lawrence  Bays,  eastern  Siberia. 

Variety  fabricii  Moller.      Greenland  1    Ungava  ! 

Labrador. 

Variety  alaskensis  Pilsbry.     Yukon  drainage,  Lake 

Fig.  39.    Eu-     Lindeman    to    Point    Romanof    and     St.    Michael, 

conulus     trochi-     Alaska  ;  Dyea  valley.  Southeastern  Alaska  ! 

^hrhU^VG   ^'^'         ^^^^  familiar  little  shell  has  had  various  vicissitudes 

land)'.  ^"  nomenclature.     The  wamQ  fulva  MuUer,  by  which 

it  is  best  known,  was  based,  according  to  Beck,  who 
was  custodian  of  MuUer's  types,  upon  Helix  bidentata  Gmelin,  while 
a  shell  which  MuUer  supposed  to  be  the  young,  but  did  not  figure 
or  fully  describe,  was  supposed  by  some  of  the  early  naturalists  to  be 
our  species.  Another  unfigured  species,  Helix  trochulus  Muller,  was 
thought  by  Dillwyn  to  be  identical  with  our  fulva^  but  the  measure- 
ments forbid  the  identification,  and  Pfeiffer  came  to  the  conclusion 
that  H.  trochulus  is  identical  with  the  young  tip  of  Buliminus  ob- 
scurus.     Fabricius   supposed   our  shell   to  be  identical  with  Helix 


42  LAND    AND    FRESH    WATER    MOLLUSKS 

hammonis  Strom  (1765),  but  Strom's  figure  is  widely  umbilicated  and 
so  rude  as  to  be  practically  unidentifiable. 

The  first  specific  name  which  unmistakably  applies  to  our  shell,  and 
to  it  alone,  is  the  trochiformis  of  Montagu,  which  it  seems  advisable 
to  adopt. 

Under  the  name  fulva  several  distinct  though  very  closely  allied 
forms  have  been  generally  included.  Reinhardt,  Bourguignat  and 
lastly  Pilsbry  have  thrown  additional  light  on  this  subject,  and  a  num- 
ber of  species  or  marked  varieties  are  now  recognized.  The  Helix 
chersina  of  Say  is  a  southern  form,  while  the  H.  egena  oi  Say  is 
generally  admitted  to  be  a  synonym  of  the  trochiformis . 

The  Euconulus  fabricii  of  Greenland  seems  to  be  merely  a  case 
(>i  an  offshoot  which  by  isolation  has  been  enabled  to  assume  distinctive 
characters,  which  have  hardly  reached  a  greater  than  varietal  rank. 

Genus  Zonitoides  Lehmann. 
Zonitoides  nitidus  Miiller. 

Helix  nittdaMxnASEK,  Hist.  Verm.,  11,  p.  32,  1774. 

Helix  lucida  Draparnaud,   Hist.  Moll,  de  France,  p.  103,  1805  ;  not  of  the 

Tableau,  1801. 
Hyalina  nitida  Tryon,  Am.  Joum.   Conch.,  ii,  p.  250,  pi.  iv,  fig.  24,  1866. 

—  BiNNEY,  Land  and  Fw.  Sh.  N.  Am.,  i,  p.  31,  figs.  35,  36,  1869. 
Zonitoides  nitidus  Pilsbry,  Class.  Cat.,  p.  27,  1898. 

Range.  —  Holarctic.  Europe,  northern  United  States,  British 
America,  Alaska,  Japan. 

Red  River  drift,  Manitoba  ;  Peace  River,  Athabaska  ;  Fort  Resolu- 
tion, Great  Slave  Lake ;  Seattle,  Wash. !  Klukwan,  Alaska  (Krause) . 

This  species  has  been  found  so  widely  spread  that  it  cannot  reason- 
ably longer  be  regarded  as  merely  a  European  emigrant. 

Zonitoides  arboreus  Say. 

Helix  arboreus  Say,  Nicholson's  Encyl.,  1st  Am.  edition,  pi.  iv,  fig.  4,  181 7. 
Helix arborea  Gould,  Inv.  Mass.,  p.  182,  fig.  110,  1841.  — Morse,  Am.  Nat., 

I,  p.  542,  fig.  30,  1867. 
Hyalina  arborea  Morse,  Joum.  Portland  Soc.  Nat.  Hist.,  I,  p.  14,  fig.  28,  pi. 

VI,  fig.  29,  1864. —  BiNNEY,  Land  and  Fw.  Sh.  N.  Am.,  I,  p.  33,  figs.  38- 

40,  1869. 
Helix  breweri  Nkwcomb,  Proc.  Cal.  Acad.  Sci.,  iil,  p.  118,  1864. 

Range.  —  North  America  generally  and  Japan. 

Labrador ;  Ontario  ;  English  River  !  Keewatin  and  Moose  Factory  ; 
Carberry  and  Lake  of  the  Woods,  Manitoba ;  Laggan  and  Red  Deer, 
in  Alberta ;  Great  Slave  Lake  !  Oregon,  at  Weston  !  Vancouver  Island 
at  Victoria  !  Departure  Bay  !  Nanaimo  !  Comox !  Union  Bay  !  etc. ; 
in  Alaska  at  Unalaska !  Petropavlovsk,  Kamchatka!  Japan  (Hirase). 


FAMILY    ZONITID^  43 

Zonitoides  randolphi  Pilsbry. 

Zonitoides  randolphi  Pilsbry,  Nautilus,  xii,  p.  87,  1898. —  Randolph,  op. 
cit.,  p.  no,  1899. 

Range.  —  Lake  Lindeman,  headwaters  of  the  Yukon,  British 
America. 

I  have  not  seen  this  species,  which  is  less  than  5  mm.  in  diameter. 
It  has  not  been  figured. 

Zonitoides  minusculus  Binney. 

Helix  minuscula  Binney,  Boston  Joum.  Nat.  Hist.,  iii,  p.  435,  pi.  xxii,  fig. 

4,  1840. —  Morse,  Am.  Nat.,  i,  p.  543,  fig.  35,  1867. 
Pseudohyalina  minuscula  Morse,  Joum.  Portland  Soc.  N.  Hist.,  i,  p.  16,  fig. 

34,  pi.  VII,  fig.  35,  1864. 

Range.  —  North  America  generally. 

Red  River  of  the  North,  Manitoba ;  Victoria  and  Departure  Bay  ! 
Vancouver  Island ;  Berg  Bay,  Muir  Inlet !  Alaska ;  Coal  Harbor, 
Unga  Island,  Shumagins  !  Rooluk  Island !  near  Unalga,  Aleutians, 
Alaska. 

Zonitoides  milium  Morse. 

Helix  milium  Morse,  Proc.  Boston  Soc.  Nat.  Hist.,  vii,  p.  28,  1859  ;  Am. 

Nat.,  I,  p.  543,  fig.  36,  1867. 
Striatura  milium  Morse,  Joum.  Portland  Soc.  Nat.   Hist., 

I,  p.  18,  figs.  41,  42,  pi.  VII,  fig.  43,  1864. 


Range. — Eastern  United  States  and  Canada.  Mani- 
toba (rare,  Hanham). 

The  report  of  this  species  from  Vancouver  Island        ^}^'  3°-   '^''"" 

,,,,  J  .^li-ii        •         r  r^        •  itoides     milium. 

was  probably  based  on  the  following  form.  Z..  minus-  ,  .     , 

^  •'  .         .  rF        •  •  from     below 

cuius  has  also  been  wrongly  identified  as  Z.  milium,  (magnified). 

Zonitoides  pugetensis  Dall. 

Patulastra  ?  {Punctumf)  pugetensis  Dall,  Nautilus,  viii.  No.  ll,  p.   130, 

Mar.,  1895. 
Zonitoides  pugetensis  Pilsbry,  Nautilus,  ix,  p.  18,  1895. 
Zonitoides  (^Pseudohyalina)  pugetensis  Dall,   Proc.  U.  S.  Nat.  Mus.,  xxiv, 

p.  500,  pi.  XXVII,  figs.  10,  12,  1902. 

Range.  —  Puget  Sound  region,  Oregon,  California. 
Seattle,  Wash. !  Nanaimo,  Vancouver  Island. 

Genus  Gastrodonta  Albers. 

*Gastrodonta  gularis  Say } 

Helix  gularis  J.  de  C.  Sowerby,  in  Richardson,  Fauna  Bor.  Am. ,  iii,  p. 
315,  1836  (nude  name). 

Range.  —  Lake    Superior,    Winnipeg,    and    Saskatchewan    River 
(Sowerby). 


44  LAND    AND    FRESH   WATER   MOLLUSKS 

This  name  is  doubtless  one  given  by  Sowerby  to  some  unknown 
shell,  as  it  is  as  certain  as  almost  anything  can  be,  that  Helix  gularis 
Say  was  never  collected  in  the  region  referred  to. 

Genus  Pristiloma  Ancey. 
Pristiloma  lansingi  Bland. 

Zonites  lansingi  Bland,  Ann.  Lye.  Nat,  Hist.  N.  Y.,  xi,  p.  74,  figs,  i,  2,  1875. 
Microphysa  lansingi  Bi-asKY ,  Man.  Am.  Land  Sh.,  p.  90,  figs.  55,  56,  1885. 
Pristiloma  lansingi  Pilsbry,  Class.  Cat.,  p.  29,  1898. 

Range.  —  Oregon,  Washington,  British  Columbia. 
Astoria,  Oregon  !  Seattle,  Wash. !  common  at  Victoria  !  and  Nan- 
aimo !  Vancouver  Island. 

Pristiloma  steamsii  Bland. 

Zonites  siearnsii'Ri.K^Xi,  Ann.  Lye.  Nat.  Hist.  N.  Y.,  xi,  p.  76,  fig.  3,  1875, 

(Astoria,  Oregon). 
Microphysa  steamsii  Binney,  Bull.   Mus.  Comp.  Zool.,  xi,  No.  8,  p.  147,  pi. 

II,  figs.  N,  o,  1883  ;  XIII,  No.  2,  p.  44,  1886. 
Pristiloma  stearnsi  Binney,   Bull.  Mus.    Comp.    Zool.,  xxil.   No.  4,  p.    176, 

1892. 

Range.  —  Columbia  River  to  Dyea,  Alaska. 

Astoria  and  Portland,  Oregon !  Olympia,  Wash. !  Comox !  Union 
Bay !  and  Salt  Spring  Island,  British  Columbia ;  Killisnoo,  Por- 
tage Bay,  Anuk,  Dyea  valley,  Klehini  and  Klukwan,  Southeastern 
Alaska. 

Pristiloma  taylori  Pilsbry. 

Pristiloma  taylori  Pilsbry,  Proc.  Acad.  Nat.  Sci.  Phila.,  for  1899,  p.  185,  pi. 
IX,  figs.  6,  7,  8  (Nanaimo). 

Range.  —  Oregon,  Washington  and  British  Columbia  at  Nanaimo, 
Vancouver  Island. 

♦Pristiloma  pilsbryi  Vanatta. 

Pristiloma pilsbryi  Yx^XTTX,   Proc.  Acad.  Nat.  Sci.  Phila.,  for  1899,  p.  120, 
fig.  I  (3  views). 

Range.  —  Portland,  Oregon. 

*Pristiloma  idahoense  Pilsbry. 

Pristiloma  idahoense  Pilsbry,  Proc.  Acad.  Nat.  Sci.  Phila.,  for  1902,  p.  593, 
(Weiser  Canyon). 

Range.  —  Idaho,  in  Washington  and  Boise  counties  at  Weiser 
Canyon  and  Big  Payette  Lake. 

This  and  the  preceding  species  will  probably  be  found  within  our 
area  when  it  is  thoroughly  explored. 


FAMILY   LIMACID^  45 

Pristiloma?  arctica  Lehnert. 

Hyalina  arctica  Lehnert,  Science  Record,  ii,  p.  172,  June  16,  1884. 
f  Conulus  arcticus  Dall,  in  Pilsbry ,  Proc.  Acad.  Nat.  Sci.  Phila. ,  for  1 899,  p.  1 87. 
?  Pnstiloma  arctica  Pilsbry,  Proc.  Acad.  Nat.  Sci.  Phila.,  for  1899,  p.  186, 
pi.  IX,  figs.  3,  4,  5. 

Range. — Yakutat  Bay,  Alaska,  to  Point  Barrow. 

Point  Barrow,  Lat.  71°  25'  N. !  Unalaska  !  Coal  Harbor,  Unga 
Island,  Shumagins  !  Orca,  Prince  William  Sound  !  and  Yakutat  Bay, 
Alaska ! 

This  may  prove  to  be  a  depressed  Euconulus  when  the  animal  is 
anatomically  examined. 

The  species  was  formerly  confused  with  P.  stearnsii.  It  occurs 
in  the  moss  of  the  tundra  near  Point  Barrow,  where  at  most  it  can 
have  but  three  months  of  activity  out  of  the  whole  year. 

Family  LXMACID.*;. 
Genus  Agriolimaz  Morch. 


Fig.  31.     AgrioUmax  agrestis  L. 

Agriolimaz  agrestis  Linn6. 

Limax  a£^rgstis  LisnK,  Syst.  Nat.,  ed.  x,  p.  652,  1758. —  Forbes  and  Han- 
ley,  Brit.  Moll.,  IV,  p.  13,  pi.  DDD,  fig.  3,  1853. 

Range.  —  Both  coasts  of  America,  introduced  from  Europe. 
Victoria,  B.  C. !  Manitoba  ;  Ungava  ! 

Agriolimaz  hyperboreus  Westerlund. 

Umax  hyperboreus  Westerlund,  Land  och  Sotv.  Moll.  Sibiriens,  p.  21,  1876. 

—  BiNNEY,   Man.   Am.   Landsh.,    p.   473,   fig.   416,    1885;  Bull.    Mus. 

Comp.  Zool.,  XIII,  No.  2,  p.  42,  1886  ;  xix.  No.  4,  p.  205,  fig.,  pi.  viii, 

fig.  F,  1890. 
Umax  {AgrioUmax)  hyperboreus  Dall,   Proc.  U.  S.  Nat.   Mus.,  for  1886,  p. 
202,  Oct.,  1886. 

Range.  —  The  Arctic   and   boreal   regions   of   both  hemispheres. 

Bering  Id. !  Kamchatka !  Chukchi  Peninsula !  Alaska  at  Norton 
Sound !  Nushagak !  Unalaska !  Coal  Harbor,  Shumagins  !  St.  Paul 
Island,  Bering  Sea  !  Kadiak  Island  !  Sitka  !  and  Cape  Fox  !  In  Van- 
couver Island  at  Comox  ;  Seattle,  Wash. ;  Alberta  at  Laggan,  altitude 
5,200  feet;  Manitoba;  Ungava,  Labrador ! 

This  little  black  slug  is  the  prevalent  and  almost  the  only  animal  of 
its  kind  in  the  higher  latitudes  of  North  America.    It  has  been  referred 


46  LAND    AND    FRESH    WATER    MOLLUSKS 

to  A.  campcstris  as  a  variety  by  some  authors,  but  it  is  at  least  the 
only  form  of  catnpestris  known  in  the  north  and  seems  distinct  enough 
to  be  recognized  as  a  species. 

Agriolimax  berendti  Strebel. 

Limax  berendti  Strebel  and  Pfeffer,  Max.  1.  u.  sussw.  Conch.,  iv,  p.  22, 

pi.  IX,  figs.  10,  12  ;  pi.  XV,  fig.  3,  1880. 
Limax  hemphilli  Binney,  3d  Suppl.  Terr.  Moll.,  v,  p.  205,  pi.  viii,  fig.  e  ; 

pi.  I,  fig.  13,  pi.  II,  fig.  3,  1890;  Bull.   Mus.  Comp.  Zool.,  xxil,  No.  4, 

p.  166,  pi.  Ill,  fig.  I,  1892. 

Range.  —  Guatemala  to  British  Columbia. 

Genus  Amalia  Moquin  Tandon. 
*Amalia  hewstoni  Cooper. 

Limax  {Amalia)  hewstoni  Cooper,  Proc.  Acad.  Nat.  Sci.  Phila.,  for  1872,  p. 

145,  pi.  Ill,  figs.  BI-B5. 
Amalia  kewstoni  Fii.sbry,  Class.  Cat.,  p.  29,  1898. 

Range.  —  San  Diego  to  Seattle.     San  Francisco,  Calif. ! 

This  form  may  perhaps  be  an  evolution  from  imported  specimens 
of  the  European  A.  gagates.  It  probably  extends  into  British 
Columbia. 

Family  ARIONIDJE. 

Genus  Prophysaon  W.  G.  Binney. 

Prophysaon  andersoni  Cooper. 

Arionf  andersoni  Coovkr,  Proc.  Acad.  Nat.  Sci.  Phila.,  for  1872,  p.  148,  pi. 

Ill,  figs.  FI-F5.  —  Pilsbry,  op.  cit.  for  1898,  p.  245,  pi.  x,  figs.  18-22  ; 

pi.   XI,    figs.   28,   29  ;    pi.  XIII,   figs.    59-62  ;  pi.   XVI,   figs.  92-93,    1898. 

Not  P.  andersoni.  — Binney,  in  2d  Suppl.  Terr.  Moll.,  p.  42. 
Prophysaon  andersoni  '&Vii'ii%\,  3d  Suppl.  Terr.   Moll.,   v,  p.  208,  pi.  iil,  fig. 

I,  pi.  VII,  fig.  c,  pi.  I,  fig.  3,  pi.  IX,  figs.  I,  J,  1890. 
Prophysaon  andersoni  vars.  marmoratum  and  suffusum  Cockerell,  The  Con- 

chologist,  II,  pp.  72,  118. 
Prophysaon  hemphilli  Bland  and  Binney,  Ann.   Lye.  Nat,  Hist.  N.  Y.,  x, 

p.  295,  pi.  XIII,  excluding  fig.  5. 
Prophysaon  pacificum  et  P.  flavum  Cockerell,  Nautilus,  iii,  p.  iii,  Feb., 

1890. — Pilsbry,  op.  cit.,  p.  246,  1898. 
Prophysaon  andersoni  Yzx.  pallidufn  Cockerell,  Nautilus,  v,  p.  31,  July,  1891. 

Range.  —  San  Francisco  north  to  Alaska  and  eastward  to  Idaho. 

Variety  pallidum  Cockerell,  Vancouver  Island  !  British  Columbia ; 
Cape  Fox,  Alaska ! 

Type  (^andersoni')  Victoria  and  Nanaimo,  British  Columbia. 

Var,  pacificum  Cockerell,  Victoria,  B.  C. ! 

I  have  followed  Dr.  Pilsbry's  arrangement  of  the  varying  forms  of 
this  remarkable  self -amputating  slug. 


FAMILY    ARIONID^  47 

*  Prophysaon  foliolatum  Gould. 

Avion  foliolaius  Gould,  Moll.   U.  S.   Expl.  Exped.,  p.  2,  pi.    i,  figs,  ^a,  2b, 

1852 :    Puget  Sound. 
Phenacarion  foliolatus  Cockerell,  Nautilus,  iii,  p.  127,  Mar.,  1890. 
Phenacarion  hemphilli  ^ .  G.  Binney,  3d  Suppl.  Terr.  Moll.,  v,  p.   208,  pi. 

VIII,  fig.  c,  IX,  fig.  H  ;  4tli   Suppl.,  p.  183  ;  not  Prophysaon  hemphilli 

Bland  and  Binney. 
Prophysaon  foliolatum  (Gould)  Pilsbry,   Proc.  Acad.   Nat.  Sci.   Phila.,  for 

1898,  p.  248,  pi.  X,  figs.  15,  16,  17;  pi.  XI,  fig.  32;  pi.  XIII,  figs.  55,  56, 

57,  58;  pi.  XIV,  fig.  70;  pi.  XV,  fig.  80;  pi.  XVI,  figs.  90,  98. 

Range.  —  Puget  Sound  region. 

Prophysaon  humile  Cockerell. 

Prophysaon  humile  Cockerell,  Nautilus,  ill,  p.    112,  Feb.,  1890. —  W.  G. 

Binney,  3d  Suppl.  Terr.  Moll.,  v,  p.  211,  pi.  vii,  figs,  e,  g,  l,  m,  1890. 

Pilsbry,  Proc.  Acad.  Nat.  Sci.  Phila.,  for  1898,  p.  251,  pi.  xvi,   fig.  97. 
Prophysaon  fasciatum  Cockerell,  in  Binney,  3d  Suppl.  Terr.    Moll.,  v,  p. 

209,  pi.  VII,  fig.  A,  1890. — Pilsbry,  op.  cti.,  p.  251,  pi.  x,  figs.  23-27  ; 

pi.  XI,  fig.  34  ;  pi.  XII,  figs,  37-40;  pi.  XVI,  figs.  91,  94-96. 
Prophysaon  fasciatum  WSJ.  obscurum  Cockerell,  The  Conchologist,  11,  p.  119, 

Mar.  1893. 

Range.  —  Northern  Idaho  to  Puget  Sound  and  northw^ard  to  Alaska. 

P.  humile  Loring,  Alaska  !  Seattle  ! 

P.  fasciatum  Old  Mission,  Idaho;  Chehalis  and  Seattle,  Wash. 

•Prophysaon  coeruleum  Cockerell. 

Prophysaon  coeruleum  Cockerell,  Nautilus,  iii,  p.  112,  Feb.,  1890. —  Bin- 
ney, 3d  Suppl.  Terr.  Moll.,  v,  p.  209,  pi.  vii,  figs,  i,  j.  May,  1890. — 
Pilsbry,  Proc.  Acad.  Nat.  Sci.  Phila.,  for  1898,  p.  253,  pi.  ix,  figs.  7-1 1; 
pi.  XI,  fig.  30;  pi.  XIII,  figs.  51-53  ;  pi.  xvi,  fig.  86,  Nov.,  1898. 

P.  cceruleum  var.  dubium  Cockerell,  loc.  cit.,  1890. 

Range.  —  Portland,  Oregon  ;   Seattle  and  Olympia,  Wash. 

Genus  Ariolimax  Morch. 

Ariolimax  columbianus  Gould. 

Limax  columbianus  GouLD,  Terr.  Moll.,  11,  p.  43,  pi.  lxvi,  fig.  i,  185 1  ; 
Moll.  U.  S.  Expl.  Exp.,  p.  3,  fig.  I,  a,  b,  1852. 

Ariolimax  columbianus  Morch,  Mai.  Bl.,  vi,  p.  no,  1859. — Binney,  Am. 
Joum.  Conch.,  i,  p.  48,  pi.  vi,  figs.  11-13,  1865  ;  Land  and  Fw.  Shells 
N.  Am.,  I,  p.  279,  fig.  499,  1869  ;  Man.  Am.  Landsh.,  p.  98,  figs.  58- 
61,  1885. — Pilsbry,  Proc.  Acad.  Nat.  Sci.  Phila.  for  1896,  p.  342; 
1898,  p.  235,  pi.  XV,  fig.  81;  pi.  XIV,  fig.  66;  pi,  XV,  figs.  73,  74,  1898. 

Range. —  Santa  Barbara,  northward  to  Sitka, Victoria,  and  Nanaimo. 

Malcolm  Island  and  Broughton  Strait,  British  Columbia  ;  SE.  Alaska 
(to  Cross  Sound })  Klawak,  Prince  of  Wales  Archipelago !  Sitka, 
Alaska  !  and  probably  north  to  Cross  Sound  and  Icy  Strait,  or  even 
Lituya  Bay. 


48  LAND    AND    FRESH    WATER    MOLLUSKS 

This  is  the  common  slug  of  British  Columbia  and  Alaska,  found  in 
damp  places  in  the  wooded  region.  It  varies  from  dark  maculate  to 
yellowish  olive,  and  when  full  grown  may  reach  a  length  of  eight  or 
nine  inches,  when  fully  extended.  It  is  very  fond  of  the  leaves  of  the 
Alaskan  skunk  cabbage,  a  taste  shared  by  bears  and  the  Alaskan  deer. 
It  produces  a  profuse  and  most  tenacious  slime.  When  the  Indians 
wish  to  catch  the  ruby -throat  humming  bird  they  gather  two  or  three 
of  these  slugs  and  whip  them  with  small  bare  twigs.  Under  this 
treatment  slime  is  given  off  in  large  quantity  and  adheres  to  the  twigs, 
which  are  afterward  placed  among  the  flowers  visited  by  the  hummers. 
If  they  alight  on  one  of  the  twigs  they  cannot  escape  from  the  ad- 
hesiveness of  this  singular  birdlime.  It  is  said  one  of  the  ancient  chiefs 
had  a  cape  entirely  covered  with  the  resplendent  plumage  of  the  male 
ruby-throat,  and  which  was  regarded  as  incredibly  valuable.  The 
black  spotted  form  seems  to  have  been  named  maculatus^  by  Cockerell, 
and  the  yellow  mutation  stramineus^  by  Hemphill,  but  they  occur  in- 
discriminately in  Alaska  and  are  probably  only  individual  color-muta- 
tions. 

♦Ariolimax  steindachneri  Babor. 

Ariolimax  steindachneri  'Rabo'R,  Ann.  K.K.  Naturh.  Hof-Museum,  Wien,  xv, 
p.  85,  1900. 

Range.  —  Puget  Sound. 

I  am  unable  to  state  whether  this  Is  distinct  or  one  of  the  mutations 

of  A.  columhianus. 

Genus  Hemphillia  Bland  and  Binney. 


Fig.  32.     Hemphillia  glandulosa  Binney. 

*  Hemphillia  glandulosa  B.  and  B. 

Hemphillia  glandulosa  Bland  and  Binney,  Ann.  Lye.  Nat.  Hist.  N.  Y.,  x, 
p.  209;  pi.  IX,  figs.  I,  3,  5,  15,   16,  17,  1872. — PiLSBRY  and  Vanatta, 
Proc.  Acad.  Nat.  Sci.  Phila.,  for  1898,  p.  233,  pi.  ix,  figs,  i,  2  ;  pi.  xil, 
figs.  49,  50. 
Range. — Astoria,  Oregon,  and  Puget  Sound  region. 

*  Hemphillia  camelus  Pilsbry  and  Vanatta. 

Hemphillia  camelus  Pilsbry  and  Vanatta,  Nautilus,  xi,  p.  44,  Aug.,  1897  ; 
Proc.  Acad.  Nat.  Sci.  Phila.,  for  1898,  p.  234,  pi.  ix,  figs.  3,  4  ;  pi.  xii, 
figs.  41,  42  ;  pi.  XVI,  fig.  85. 


FAMILY   ENDODONTID^  49 

Range.  —  Northern  Idaho,  at  Old  Mission.  Like  other  species  of 
northern  Idaho  this  probably  extends  across  the  parallel  into  British 
America. 

Family  ENDODONTID^. 

Genus  Pyramidula  Fitzinger. 
Subgenus  Patula  Held. 
Pyramidula  solitaria  Say. 

Helix  solitaria  Say,  Journ.  Acad.  Nat.   Sci.   Phila.,  11,  p.    157,  1821. — BlN- 

NEY,  Terr.   Moll.  U.  S.,  i,  p.   254,  pi.  vril,  figs.  6-10 ;  11,  p.  208,  pi. 

XXIV,  1851. 
Patula  solitaria  (Say)  Binney,   Man.  Am.  Landsh.,  p.   254,  figs.  263,  267, 

268,  1885. 
Helix  limitaris  Dawson,  Rep.  Brit.  N.  Am.  Boundary  Survey,  Geology,  pp. 

347-350.  1875. 
Pyramidula  solitaria  limitaris  Pilsbry,  Class.  Cat.  Am.  Landsh.,  p.  31,  1898. 
Patula  solitaria  var.  occidentalis  \o^  Martens,  yf</^  Pilsbry,  1.  c,  p.  31,  1898. 

Range.  —  Arkansas  north  to  Ohio,  west  to  eastern  Oregon,  and 
northward  in  Alberta. 

Var.  limiiaris^  Waterton  Lake,  Rocky  Mts.  in  Alberta ;  northern 
Idaho. 

Var.  occidentalism  Dalles  of  the  Columbia  near  Fort  Vancouver; 
Coeur  d'Alene  Mts.,  Idaho. 


34 
Figs.  33-35.     Pyramidula  alternata  Say. 

♦Pyramidula  alternata  Say. 

Helix  alternata  Say,  Nicholson's  Encycl.,  ist  Am.  ed.,  11,  pi.  i,  fig.  2,  1817. 

—  Binney,  Land  and  Fw.  Sh.  N.  Am.,  i,  p.  73,  figs.  122-129,  1869. 
Anguispira  alternata  Morse,  Journ.  Portland  Soc.  N.  Hist.,  I,  p.  11,  fig.  15, 

pi.  IV,  fig.  16,  1864. 
Helix  dubia  Shepard,  Trans.  Lit.  Sci.  Soc.  Quebec,  i,  p.  194,  1829. 

Range.  —  Eastern  North  America  as  far  north  as  Nova  Scotia, 
Lower  Canada,  and  the  international  boundary. 

Lake  of  the  Woods  1  (Kennicott)  ;  Canso,  Nova  Scotia  (^Jide  Bin- 
ney). 

Binney  {of.  cit..,  pp.  74,  76)  gives  the  northeastern  range  of  this 
species  as  Labrador,  but  Canso,  where  his  specimens  were  obtained,  is 


50  LAND    AND    FRESH    WATER    MOLLUSKS 

in  Nova  Scotia,  not  Labrador.     I  have  no  authentic  record  of  this 
species  north  of  Lake  of  the  Woods. 

Subgenus  Gonyodiscus  Fitzinger. 
Pyramidula  striatella  Anthony. 

Helix  siriatella  AnTHoyiY,  Boston  Joum.   Nat.  Hist.,  iii,  p.  278,  pi.  iii,  fig. 

2,  1840. —  Gould,  Inv.  Mass.,  p.  178,  fig.  112,  1841. 
Patula  striatella  Binney,  Man.  Am.  Land  Shells,  p.  69,  figs.  28,  29,  1885. 
Pyramidula  {Gonyodiscus)  striatella  Pilsbry,  Class.  Cat.  Am.  Landsh.,  p.  32, 

1898. 

Range. — Kansas  northward  to  Great  Slave  Lake  and  from  New 
England  to  the  Sierra  Nevada,  and  south  to  Arizona. 

Woods  of  the  Winnipeg  basin.  Turtle  Mt.,  Lake  of  the  Woods! 
English  River  !  Manitoba  ;  Moose  Factory  !  James  Bay  ;  Great  Slave 
Lake  at  Fort  Resolution  !  in  Alberta  at  Laggan,  Red  Deer,  Olds, 
and  McLeod,  west  to  the  Selkirk  Range. 

It  is  difficult  to  distinguish  immature  specimens  of  this  species  from 
P.  cronkhitei  Newc. ,  but  when  full  grown  perfect  specimens  are  com- 
pared it  is  seen  that  striatella  is  a  smaller  shell  with  a  proportionately 
larger  umbilicus,  it  is  of  a  richer  brown  color,  more  regularly  and 
elegantly  ribbed  and  more  polished  or  glistening  on  the  surface.  The 
animal  of  striatella  shows  no  red  maculations  through  the  translucent 
shell  when  living,  such  as  are  seen  in  P.  ruderata. 

Pyramidula  cronkhitei  Newcomb. 

Helix  cronkhitei  ^Y.\NCOU'&,  Proc.  Cal.  Acad.  Sci.,  ill,  p.  180,  1865. 

Patula  cronkhitei  Tryon,   Am.  Joum.  Conch.,   11,  p.   263,  1866. — Binney, 

Man.  Am.  Landsh.,  p.  70,  fig.  30,  1885. 
Pyramidula  striatella  cronkhitei 'Pii.sbky,  Class.  Cat.  Am.  Landsh.,  p.  32,  1898. 
Patula  pauper  BiaviKY  {ex  parte),  Man.  Am.  Landsh.,  p.  187,  1885. 

Range.  — Nevada  and  California  in  the  wooded  mountain  region  to 
6,000  feet ;  Klamath  Lake  and  valley,  Oregon,  and  northward. 

British  Columbia  at  Nanaimo  ;  Lake  Lindeman,  Yukon  Territory ; 
in  Alaska  at  Sitka  !  Chilkat  Inlet !  and  valley ;  Chilkoot  Inlet !  and 
valley  !  shores  of  Yakutat  Bay  !  English  Bay  (Merriam)  !  and  St. 
Paul,  Kadiak  Island  !  Popof  and  Unga  Islands  !  Shumagins  ;  Chika 
Rocks  !  and  Akutan  Island  !  Akutan  Pass  ;  Unalaska  (Dall,  Elliott, 
Kincaid,  Turner)  ! 

Mr.  Binney  observes  that  this  species  is  larger,  of  a  lighter  color,  is 
more  coarsely  (and  I  may  add  more  irregularly)  striated  than  P. 
striatella.  It  also  has  when  full  grown  a  larger  shell  and  relatively 
smaller  and  deeper  umbilicus.  I  am  obliged  to  confess  that  I  am  not 
able  to  distinguish  shells  long  dead  from  those  of  P.  ruderata^  which 


FAMILY    ENDODONTID^  5 1 

replaces  this  species  on  Bering  Island  and  in  Kamchatka.  But  when 
the  animals  are  living  P.  ruderata  shows  through  the  translucent  shell 
deep  red  or  red-brown  radiating  maculations,  which  are  situated  on 
the  mantle.  After  the  shells  have  been  dead  some  time  this  macula- 
tion  disappears.  Now  the  living  7^.  cronkhitei  do  not  show  any  such 
color-markings.  The  presence  of  the  latter  led  Mo  relet  to  name  an 
immature  ruderata^  Helix  Jloccata.  The  shell  figured  by  von  Martens 
in  the  Conchologische  Mittheilungen  under  the  name  of  Jloccata  does 
not  agree  with  Morelet's  original  diagnosis,  and  was  not  found  by  me 
during  much  energetic  collecting  at  his  locality,  Petropavlovsk,  Kam- 
chatka, in  1865.  If,  as  stated  by  von  Martens,  it  really  comes  from 
the  original  lot  collected  by  Morelet  it  is  evident  that  his  diagnosis 
(which  calls  for  a  shell  with  an  angular  periphery  like  young  ruderata^ 
was  founded  on  a  mixture,  of  which  young  ruderata  probably  formed 
a  part.  But  I  am  inclined  to  believe  that  von  Martens  was  misled  in 
regarding  the  shell  he  figured  to  be  a  native  of  Kamchatka. 

Pyramidula  pauper  Gould  was  described  from  the  same  locality 
as  Morelet's  Jloccata^  and  is  undoubtedly  the  same  as  the  shell  I  have 
called  ruderata^  following  Morelet,  Middendorff  and  others.  But  the 
P.  cronkhitei  from  Unalaska  and  other  places  in  Alaska  which  has 
been  called  pauper  by  Dr.  Cooper  and  others,  is  our  American  shell. 
Mr.  Binney  thought  it  different  from  P.  cronkhitei^  but  after  much 
study  and  consideration  I  cannot  confirm  this  opinion. 

Subgenus  Planogyra  Morse. 

♦Pyramidula  asteriscus  Morse. 

Helix  asteriscus  Morse,  Proc.  Boston  Soc.  Nat.  Hist.,  vi,  p.  128,  1857  ;  Am. 

Nat.,  I,  p.  546,  fig.  43,  1867. 
Planogyra  asteriscus  Morse,  Journ.  Portland  Soc.  Nat.   Hist.,  i,  p.   24,  figs. 

51,  52  ;  pi.  II,  fig.  5  ;  pi.  VIII,  fig.  53,  1864. 
Patula  asteriscus  ^\H^E\ ,  Man.  Am.  Landsh.,  p.  186,  figs.  185,  186,  1885. 
Pyramidula  (^Planogyra)  asteriscus  Pilsbry,  Class.  Cat.  Am.  Landsh.,  p.  33, 

1898. 

Range.  —  Maine  ;  Provinces  of  Quebec  and  Ontario,  Canada;  Van- 
couver Island  }  Tacoma,  Wash.  } 

This  species  has  been  reported  from  British  Columbia  and  Wash- 
ington, but  it  seems  the  identification  is  somewhat  doubtful,  and  the 
shells  were  probably  Punctum  clappi  Pilsbry. 

Genus  Oreohelix  Pilsbry. 
Oreohelix  strigosa  Gould. 

Helix  strigosa  Gould,  Proc.  Boston  Soc.  Nat.  Hist.,  il,  p.  166,  1846  :  Moll.  U. 
S.  Expl.  Exped.,  p.  36,  fig.  41,  1852. —  Binney,  L.  and  Fw.  Sh.  N.  Am., 
I,  p.  72,  1869. 


52  LAND   AND    FRESH    WATER    MOLLUSKS 

Helix  cooperi  Binney,  Proc.  Acad.  Nat.  Sci.   Phila.,  for  1858,  p.  118;  Land 

and  Fw.  Sh.  N.  Am.,  i,  p.  78,  figs.  132-137,  1869. 
Helix  haydeni  GhBB,  Am.  Joum.  Conch.,  v,  p.  24,  pi.  viii,  fig.  i,  1869. 
Anguispira  bruneri  A^c^Y ,  La  Nature,  in,  p.  468,  Sept.,  1881. 
Oreohelix  strigosa  Pilsbry,  Nautilus,  xvii,  No.  11,  p.  131,  footnote,  1904. 

Range. — Type  at  Spokane,  Wash.,  also  in  the  Rocky  Mountain 
region  from  northern  Mexico  to  and  somewhat  beyond  the  49th  parallel 
westward  from  the  Lake  of  the  Woods. 

Var.  cooperi.,  Lake  of  the  Woods,  and  westward  to  the  Rockieis 
near  the  49th  parallel. 

\ 2iX .  stantoni  V>^  (1905).  Thirty-three  miles  southeast  of  Medi- 
cine Hat,  Assiniboia,  near  top  of  Cypress  Hills,  altitude  4,700  feet; 
latitude  about  49°  30',  west  longitude  1 10°  10'. 

The  variety  stantoni  is  dwarfed,  measuring  in  maximum  diameter 
lO.o,  minimum  8.5,  and  height  8.0  mm.,  with  about  five  whorls,  a 
peripheral  brown  band  with  a  narrower  one  above  and  sometimes 
others  on  the  base,  the  remainder  ashy,  rudely  incrementally  striate, 
with  rounded  periphery  and  deep  narrow  (i  mm.)  umbilicus.  It  is 
very  similar  to  some  varieties  of  the  European  H.  virgata  Da  Costa. 
Eight  specimens  were  collected  by  Dr.  T.  W.  Stanton  in  1903. 

A  large  number  of  names,  varietal  and  other,  have  been  given  to  the 
mutations  of  this  species,  which  barely  enters  the  region  covered  by 
this  memoir,  at  its  southern  border  near  the  Rocky  Mountains.  The 
group  is  viviparous,  and  the  young  attain  a  large  size  before  extrusion. 


Genus  Helicodiscus  Morse. 

Helicodiscus  lineatus  Say. 

Helix  lineata^Kx,  Joum.  Acad.  Nat.  Sci.  Phila.,  i,  p.  18,  1819. — Gould,  Inv. 

Mass.,  p.   179,  fig.  103,   1 84 1. — Morse,  Am.  Nat.,  i,  p.  546,   fig.  44, 

1867. 
Planorbis parallelus  Say,  Proc.  Acad.  Nat.  Sci.  Phila.,  li,  p.  164,  1821. 
Helicodiscus  lineatus  yiOKSK,    Joum.   Portland  Soc.  Nat.   Hist.,  i,  p,  25,  figs. 

61,  62,  pi.  II,  fig.  3;  pi.  VII,  fig.  63,  1864. —  Binney,  Man.  Am.  Landsh., 

p.  75,  figs.  34-37  A,  1885. 

Range.  —  New  Mexico  to  Manitoba,  New  England  to  California. 
Reported  as  rare  in  Manitoba  by  Hanham. 


-^^t 


Fig.  36.    Helicodiscus  lineatus,  shell  and  animal  (magnified). 


FAMILY    ENDODONTID.<E  53 

Genus  Punctum  Morse. 

Punctum  pygmaeum  Draparnaud. 

Helix  pygmaa  Draparnaud,  Hist.  Moll.,  p  114,  pi.   viii,  figs.  8,   9,  10, 

1805. 
Helix  minutissima  Lea,  Trans.  Am.  Phil.  Soc,  ix,  p.  17  ;  Proc,  li,  p.  82, 

1841. — BiNNEY,  Terr.  Moll.,  iv,  p.  100,  pi.  Lxxvii,  figs.  6,  7,  1859. — 

Morse,  Am.  Nat.,  i,  p.  546,  fig.  46,  1867. 
Punctum  minutissimum  Morse,  Journ.  Portland  Soc.  Nat.   Hist.,  i,  p.  27, 

figs.  69,  70,  pi.  VIII,  fig.  71,  1864. 
Microphysapygmcea  Binney,  Man.  Am.  Landsh.,  p.  71,  figs.  31-33,  1885. 
Punctum  PygmcEum  Pilsbry,  Class.  Cat.  Am.  Landsh  ,  p.  33,  1898. 

Range,  —  United  States  generally;  Quebec;  Manitoba;  Victoria, 
Vancouver  Island.     Europe. 

♦Punctum  randolphi  Dall. 

Pyramidulaf  randolphi  TiKiA.,  Nautilus,  viil,  p.  130,  Mar.,  1895. 
Punctum  randolphi  YivSKKY,  Nautilus,  ix,  p.  18,  June,  1895. — Dall,  Proc. 
U.  S.  Nat.  Mus.,  xxiv,  p.  500,  pi.  xxvii,  figs.  7,  8,  9,  1902. 

Range.  —  Seattle,  Wash. 

Probably  exists  throughout  the  Puget  Sound  region  and  adjacent 
British  Columbia. 

Punctum  clappi  Pilsbry. 

Punctum  clappi  Vii.SBK\,  Nautilus,  xi,  p.  133,  Apr.,  1898  ;  Class.  Cat.  Am. 
Landsh.,  p.  33,  1898. 

Range.  —  Oregon,  Washington,  Vancouver  Island. 

Salem,  Wash. ;  Tacoma,  Wash. ;  Seattle,  Wash. ;  Nanaimo   and 

•  Comox,  Vancouver  Island. 

This  is  probably  the  shell  which  has  been  reported  as  P.  asteriscus 

Morse,  from  Vancouver  Island  and  Tacoma.     It  has  not  been  figured. 

Punctum  conspectum  Bland. 

Helix  conspecta  Bland,  Ann.   N.  Y.  Lye.  Nat.   Hist.,  vii,  p.  163,  fig.   7, 

1865. 
Zonites  conspectus  Binney,  Terr.  Moll.,  v,  p.  121,  1873  ;  Man.  Am.  Landsh., 

p.  86,  fig.  51,  1885. 
Punctum  conspectum  Pilsbry,  Nautilus,  xi,  p.  133,  Apr.,  1898  ;  Class.  Cat. 

Am.  Landsh.,  p.  32,  1898. 

Range.  —  West  America  from  middle  California  northward,  and 
east  to  the  west  slope  of  the  Rocky  Mountains.     Kamchatka. 

California  !  Oregon ;  Washington ;  Puget  Sound  region  generally  ; 
Victoria,  British  Columbia !  Departure  Bay,  Vancouver  Island ! 
Sitka !  Chilkoot  Inlet  and  valley ;  Chilkat  Inlet  i^nd  valley ;  Coal 
Harbor  !  Unga  Island,  Shumagins  ;  Unalaska  !  Alaska.  Petropav- 
lovsk !  Kamchatka  (Dall). 


54  LAND    AND    FRESH    WATER   MOLLUSKS 

The  most  common  of  the  minute  species  in  Alaska ;  often  found  in 
numbers  under  bits  of  cast-off  leather  and  chips  near  the  tops  of 
beaches.     The  Kamchatkan  specimens  are  beyond  suspicion. 

Genus  Sphyradium  Charpentier. 

Sphyradium  edentulum  Draparnaud. 

Pupa  edentula  Draparnaud,  Hist.  Moll.,  p.  59,  pi.  in,  figs.  28,  29,  1805. 
Pupa  simplex  Goui^u,  Boston  Journ.  Nat.   Hist.,  in,  p.  403,  pi.  in,  fig.  21, 

1840;  Inv.  Mass.,  p.  190,  fig.  121,  1841. 
Vertigo  simp/ex  SriUFSOii,  Shells  of  N.   Engl.,  p.  53,    1854.  —  Morse,  Am. 

Nat.,  I,  p.  670,  figs.  67,  68,  1868.  — BiNNEY,  Man.  Am.  Landsh.,  p.  191, 

fig.   195,  1885. 
J^pa  alticola  Ingersoll,  Bull.  U.  S.  Geol.  Geogr.  Survey  of  the  Terr.,  No. 

2,  p.  128,  1875  ;  ed.  II,  p.  391,  fig.,  1876.  —  BiNNEY,  Man.  Am.  Landsh., 

p.  174,  fig.  166,  1885. 
Pupa  columella  "Benson,"  var.  gredleri  Clessin,  from  Alaska,  is  probably 

S.  edentulum. 

Range. —  Northern  Europe,  Asia  and  America. 

Canada ;  heights  of  8,000  to  9,000  feet 

in  the  Rocky  Mountains,  Colorado  !    Un- 

gava    Bay,  Labrador !   Laggan,    Alberta ; 

Vancouver  Island  at  Comox,  Nanaimo  and 

Victoria  ;  Kukak  Bay, Peninsula  of  Alaska  ! 

Popof  Island  !  Shumagin  Islands  ;  Rooluk 

Island  near  Unalga  Pass,  Aleutians  !  Port 

I  -S/-     J'  y*'"'  """^  ^"'     Clarence,  Alaska!    Petropavlovsk !    Kam- 
tulum  { magnified).  '  ^ 

chatka  (Dall). 

This  species  has  a  wide  distribution  and  considerable  synonymy. 

Unidentified  Species. 

The  following  Helicidce  are  incertce  sedis. 

Helix  rudis  J.  de  C.  Sowerby  in  Richardson,  Fauna  Bor.  Am., 
Ill,  app.,  p.  315,  1836.     Nude  name. 

"  Lake  Superior,  Winnipeg  and  Saskatchewan  River." 

Helix  attenuata  J.  de  C.  Sowerby,  op.  cit.^  p.  315,  1836.  Nude 
name. 

"  Lake  Superior,  Winnipeg,  and  Saskatchewan  River." 

Helix  belcheri  Pfeiffer,  P.  Z.  S.  London,  for  1845,  p.  128;  Mon. 
Helic.  Viv.,  i,  p.  104;  Reeve,  Conch.  Icon.,  Mon.  Hehx.^  pi.  190, 
fig.  1328. 

This  species,  supposed  to  have  been  collected  by  Capt.  Belcher, 
during  his  voyage  to  the  Northwest  Coast  of  America,  has  not  been 
recognized  from  that  quarter  since ;  and  probably,  like  many  other 


FAMILY    SUCCINEID^  $5 

species  brought  home  by  Belcher  from  time  to  time,  had  got  wrongly 
labelled. 

FamUy  SUCCINEIDiE. 

Genus  Succinea  Draparnaud. 

Succinea  Draparnaud,  Tabl.  Moll.,  pp.  32,  55,  1801  ;  Hist,  des  Moll.  Terr., 

pp.    24,    29,    58,    1805.     Helix   putris   Linne   and    S.    oblonga   Drap. ; 

Blainville,  Man.,  i,  p.  455,  1825. 
<^Amphibulima  Lamarck,  Ann.   du    Museum,  vi,  p.   304,    1805;     ist  sp. 

A.  cuculata  Lam.  =^ patula  Brug.   Froriep,   Lam.  Syst.  Conch.,  p.   19, 

1807. 

<  Amphibulimtts  Montfort,  Conch.  Syst.,  11,  p.  90,  18 10. 

Lucena  Oken,  Lehrb.  d.  Naturg.,  iii,  pp.  x,  311,  312,  181 5  ;  Succinea 
putris  (L.)  Draparnaud. —  Hartmann,  in  Sturm,  Fauna  Deutschl.,  vi, 
pp.  27,  40,  54,  1 82 1,  L.  pulchella  Hartmann,  sole  ex.  Not  of  Hart- 
mann Neue  Alpina,  i,  p.  208. — Morch,  Vidensk.  Medd.,  p.  296,1864. 

Amphibulina  Hartmann,  in  Sturm,  Fauna  Deutschl.,  vi,  pp.  42,  55,  1821  ; 
1st  sp.  Helix  putris  L. 

Atnphibina  Hartmann,  Neue  Alpina,  i,  p.  208,-  1821.  — Morch,  Syn.  MolL 
Dan.,  p.  33,  1864;  Vidensk.  Meddel.  Kjob.,  p.  295,  1864;  ist  sp.  S. 
pfeifferi  Rossm. 

<  Cochlohydra  Ferussac,  Tabl.  Syst.,  pp.  xxxii,  26,  1821. 
Succinia  Gray,  in  Turton,  Man.,  2nd  ed.,  p.  no,  1840. 
Tapada  Studer,  Syst.  Verz.,  p.  11,  1820. 

Succincea  Deshayes,  Encyc.  Meth.,  11,  p.  18,  1830, /a55/m. 

>  Helisiga  Lesson,  Voy.  Coquille,  p.  316,   1829,  H  sanctahelence  Lesson, 

H.  and  A.  Adams,  Gen.  Rec.  Moll.,  11,  p.  130,  1855. 
~^  Helisigna  Mrs.  Gray,  Fig.  Moll.  An.,  iv,  pp.  55,  113,  1859. 
Neritostoma  Morch,  Vidensk.  MeddeL  Kjob.,  for  1863,  p.  294,  1864,   ist  sp. 

S.  putris  L. 
Tapada  Albers,  Heliceen,  p.  55,  1850. —  Pfeiffer,  Men.  Hd.  Viv.,  iv,  pp. 

803,  808,  1859. 
y  Brachyspira  Pfeiffer,  Mon.   Hel.  Viv.,   iv,  pp.  803,  804,  1859.     Not  of 

Ehrenberg,  1858. 

<  Truella  Pease,  P.  Z.  S.,  1871,  pp.  459,  472  ;  type  T.  elongata  Pease. 
Neritostoma  Westerlund,   Fauaa  d.   Pal.   Reg.,   11,  v,  pp.   i,  2,    1885  ;  S. 

putris  L. 
Oxyloma  Westerlund,  op.  cit.,  pp.  i,  7,  1885  ;  S.  dunkeri  (Zelebor). 
Atnphibina  Westerlund,  op.  cit.,  pp.  i,  8,  ist  sp.  S.  elegans  Risso. 
Lucena  Westerlund,  op.  cit.,  pp.  i,  14,  ist  sp.  S.  oblonga  Draparnaud. 

This  genus  has  been  divided  into  sections  on  the  basis  of  the  den- 
ticulation  of  the  jav^^,  as  follows  : 

Jawr  without  denticulations.      Oxyloma  {hungaricd). 
Jaw  with  a  single  median  denticle.     Amphibina  (^Pfeifferi) . 
Jaw  with  a  minute  median  denticle.     Lucena  {oblonga'). 
Jaw  with  three  denticles  Neritostoma.  =  Succinea  s.  s. 

According  to  this  scheme  S.  avara  is  an  Amphibina.^  S.  totteniana 
a  typical  Succinea^  while  S.  ovalis  (Say)  Morse  has  seven  denticles 
and  is  unprovided  for.     The  differences  among  the  few  species  which 


56  LAND   AND    FRESH    WATER    MOLLUSKS 

have  been  examined  are  so  great  that  it  is  probably  better  to  await  a 
more  thorough  knowledge  of  all  the  species,  in  the  light  of  which  we 
can  judge  better  whether  this  character  has  any  systematic  value  or 
not.  Our  American  species  resemble  one  another  so  closely  that  it 
seems  hardly  likely  that  there  are  any  fundamental  differences  between 
them. 

Succinea  oregonensis  Lea. 

Succinea  oregonensis  Lea,  Proc.  Am.  Phil.  Soc,  p.  32,  1841  ;  Trans.  Am. 
Phil.  Soc,  IX,  p.  5,  1844.  —  BiNNEY,  Terr.  Moll.,  11,  p.  ^T,  pi.  lxvii, 
fig.  2,  1851. — Tryon,  Am.  Journ.  Conch.,  11,  p.  235,  pi.  (11)  xvii, 
fig.  18,  1866.  —  BiNNEY,  Land  and  Fw.  Sh.  N.  Am.,  i,  p.  270,  fig.  485, 
1869. 

Range.  —  California  (to  6,500  feet  alt .) ,  Oregon,  Washington,  and 
British  Columbia. 

Victoria,  B.  C. !  Wallawalla,  Wash.  ! 

This  species  on  the  Pacific  Coast  takes  the  place  in  the  fauna 
occupied  in  the  East  by  S.  avara  Say,  which  it  much  resembles. 
The  S.  '  oregonensis '  reported  from  Winnipeg  by  Hanham  was 
probably  a  variety  of  avara.  The  surface  has  a  silky  unpolished 
appearance,  from  the  very  fine  close  wrinkles  with  which  it  is  covered, 
and  which  are  characteristic. 

Succinea  retusa  Lea. 

Succinea  retusa  Lea,  Trans.  Am.  Phil.  Soc,  v,  p.  117,  pi.  xix,  fig.  86,  1837. 

—  W.  G.  BiNNEY,  Land  and  Fw.  Sh.  N.  Am.,  i,  p.  256,  fig.  454,  1869. 

Succinea  ovalis  Gould,  Inv.  Mass.,  p.  194,  fig.  125,   1841,  not  of  Say,  1817. 

Succinea  haydeni  var.  minor  W.  G.  Binney,  Land  and  Fw. 

Sh.   N.  Am.,  I,  p.   256,  1869. — Tryon,   Am.  Journ. 

Conch.,  II,  p.  236,  1866. 

Succinea  decampi  Tryon,  Am.  Journ.  Conch.,   11,  p.  237, 

pi.  XVII,  fig.  23,  1869.  —  Binney,  /.  c,  p.  257. 

Range.  —  Northern  United  States,  from  Kentucky 
Fig.  -^S  Sue-  northward  to  Canada  and  British  America. 
ctnea retusa'Lta..  In  Manitoba  at  Carberry,  Lake  of  the  Woods  and 
Pembina  Mountain;  in  Alberta  at  Laggan  and  Red 
Deer.  Ungava,  Labrador  !  James  Bay  at  Moose  Factory  !  Lower  Sas- 
katchewan near  Lake  Winnipeg  !  Norway  House ;  York  Factory ; 
Fort  Resolution,  Great  Slave  Lake!  Yukon  River  near  old  Fort 
Yukon,  Alaska  !  Stewart  River,  Yukon  district !  Dall  River,  north  of 
the  Yukon !  Duncan  Bay,  Discovery  Passage,  British  Columbia. 

A  widespread  and  abundant  species  identified  by  comparison  of  the 
typical  specimens  or  cotypes  furnished  by  the  author  to  the  National 
Museum. 


FAMILY    SUCCINEID^  57 

Succinea  hawkinsi  Baird. 

Succinea  Aaie/kinsz  BxiKV),  Proc.  Zool.  Soc.  London,  p.  68,  1863.  —  Binney, 
Land  and  Fw.  Sh.  N.  Am.,  i,  p.  268,  fig.  481,  1869. 

Range.  —  British  Columbia  and  eastward  to  Manitoba. 

Lake  Osoyoos,  B.  C. ;  Sitka,  Alaska !  Carberry,  Manitoba !  not 
common. 

A  large  species  with  a  produced  oblique  aperture  and  acute  spire. 
Quite  close  to  S.  sillimani  Bland. 
Succinea  avara  Say. 

Succinea  avara  Say,  Rep.  Long's  Exped.,  11,  p.  260,  pi.  xv,  fig.  6,  1824. 
Succinea  vermeta  Say,  New  Harmony  Diss.,  11,  No.  15,  1829. — Tryon,  Am. 

Journ.  Conch.,  11,  p.  233,  pi.  (11)  xvii,  fig.  10,  1866. 
Succinea  wardiana  Lea,  Proc.  Am.  Phil.  Soc,  11,  p.  31,  184 1 ;  A 

Trans.  Am.  Phil.  Soc,  ix,  p.   3,   1844. — Tryon,  Am.  |^A 

Journ.   Conch.,  11,  p.  233,  pi.  (11)  xvii,  fig.  12,  i866.  W^ 

Succinea  avara  Binney,  Land  and  Fw.  Sh.  N.  Am.,  i,  p.  262,  ^^ 

fig.  468,  1869.  Fig.  39.   Suc- 

Range.  —  North  America  east  of  the  Rocky  Moun-  cine  a  avara 
tains  from  Texas  to  N.  Lat.  62".^  ^^-J"- 

Lac  des  Mille  Lacs  to  Lake  of  the  Woods ;  lower  Saskatchewan 
near  Lake  Winnipeg !  Two  Creeks,  Manitoba ;  Laggan,  Red  Deer, 
Olds,  and  McLeod,  Alberta;  Fort  Simpson,  Mackenzie  River  in  N. 
Lat.  62°  ! 

Succinea  gronlandica  Beck. 

Succinea  grbnlandica  Beck,  Index,  p.  99,  1837  ;  nude  name.  — Moller,  Ind. 
Moll.  Gronl.,  p.  4,  1842.— Morch,  Am.  Journ.  Conch.,  iv,  p.  31,  pi.  m, 
fig.  10,  1868. — Bikney,  Land  and  Fw.  Sh.  N.  Am.,  i,  p.  265,  fig.  474, 
1869. —  PossELT,  Consp.  Faunae  Gronl.,  p.  263,  1898. 

Range. — Iceland  and  Greenland. 

This  species  is  rather  close  to  retusa  Lea  but  seems  sufficiently  dis- 
tinct to  be  retained. 

Succinea  grosvenori  Lea. 

Succinea  grosvenori  Lea,  Proc.  Acad.  Nat.   Sci.   Phila,,  for  1864,  p,    109  ; 
Journ.  Acad.   Nat.   Sci.    Phila.,   n.  s.,   vi,  p.   179,   pi. 
^L  XXIV,   fig.    108,   1866. — Binney,   Land  and  Fw.   Sh. 

^^L  N.  Am.,  I,  p.  260,  fig.  462,  1869. 

^^B  Range.  —  North  America,  east  of  the  Rocky  Mts. 

^^  from  Louisiana  to  British  America  but  not  far  east  of 

Fig.  40.  Sue  ^^^  Mississippi. 

cinea  grosvenori  -kit      '     ^          -r-.       -r^            i-rkii-v 

r  WoodMt.,  Manitoba;  Egg  Lake  and  Red  Deer,  in 

Alberta  ;  upper  Mackenzie  River  at  Fort  Simpson  ! 

^Succinea  verrilli  Bland  (1865,  Binney,  L.  and  Fw.  Sh.  N.  Am.,  i,  p.  264, 
fig.  472)  is  probably  either  the  young  or  a  dwarf  form  of  this  species.  It  is  from 
Anticosti  Id. 


58 


LAND    AND    FRESH    WATER    MOLLUSKS 


The  distribution  indicated  by  the  literature  is  rather  odd  for  a  shell 
ranging  so  far  south,  but  there  is  no  way  of  clearing  up  the  doubt  at 
present. 

Succinea  rusticana  Gould. 

Succinea  rusticana  Gould,  Proc.  Bost.  Soc.  N.  Hist.,  ii,  p.  187,  1846  ;  Moll. 
U.  S.  Expl.  Exp.,  p.  28,  fig.  29,  1852. —  Tryon,  Am.  Journ.  Conch.,  11, 
p.  236,  pi.  (11)  XVII,  fig.  19,  1866. —  BiNNEY,  Land  and  Fw,  Sh,  N.  Am., 
I,  p.  269,  fig.  483,  1869. 

Range.  —  Tulare  valley,  Calif.,  northward  to  British  Columbia; 
the  variety  alas k ana  to  Alaska. 

Comox,  Vancouver  Island,  B.  C. !  Sumas  Prairie,  Fraser  River 
valley,  B.  C. ! 

Yaxieiy  alas kana  Dall,  nov.  Flats  near  St.  Michael,  Alaska  !  Point 
Romanof  !  Unalaska  !  St.  Paul,  Kadiak  Id.  1 

The  Alaskan  form  is  polished,  of  an  olive  greenish  tinge,  with  rather 
inconspicuous  lines  of  growth  ;  with  3  tumid  whorls,  the  general  form 
of  rusticana  as  figured  by  Binney,  but  shorter  and  more  tumid  ;  length 
10,  max.  diam.  8,  length  of  aperture  6.5  mm.  This  may  prove,  with 
more  material,  to  be  a  distinct  species. 

Succinea  nuttalliana  Lea. 

Succinea  nutiallia7ia  Lea,  Proc.  Am.  Phil.  Soc,  11,  p.  32,  1841.  — Binney, 
Terr.  Moll.,  11,  p.  81,  pi.  lxvii,  a,  fig.  4,  1851. — W.  G.  Binney, 
Land  and  Fw.  Sh.  N.  Am.,  i,  p.  269,  fig.  484,  1869, 

Range.  —  Oregon,  California,  Washington  and  British  Columbia. 
Victoria,  Vancouver  Island,  B.  C. 

This  species  was  also  reported  by  Randolph  from  the  Lewes  River, 
Yukon  Territory,  but  in  this  case  the  shell  was  probably  the  quite 
similar  S.  retusa  Lea. 

Succinea  obliqua  Say. 

Succinea  obliqua  Say,  Rep.  Long's  Exp.,  11,  p.  260,  pi.  xv,  fig.  7,  1824. — 
Binney,  Land  and  Fw.  Sh.  N.  Am.,  i,  p.  265,  fig.  475,  1869. 

?  Succinea  ovalis  SAY,  Journ.  Acad.  Nat.  Sci,   Phila.,  i,  p. 

15,  1817.     Not  5.  tfz/a/zj  Gould. 
Succinea  campestris  Gould,   Inv.  Mass.,  p.  195,  fig.    126, 
1841.— De  Kay,  Nat.    Hist.  N.  Y.,    Moll.,  p.    53,  pi. 
IV,  fig.  54,  1843. 
Succinea  greeri  Tryon,  Am.  Journ.   Conch.,   11,   p.   232, 
pi.  (11)  XVII,  fig.  8,  1866. 

Range.  —  From    Louisiana    to    Hudson  Bay   and 
Fig.  41.   Sue-     eastward  to  New  England  and  Gasp6,  but  not  west 
cinea  obliqua.         of  the  Mississippi  Valley. 


FAMILY    L.YMNJE1T>^  59 

Lac  des  Mille  Lacs  to  Lake  of  the  Woods  !  Halifax,  N.  S. ;  Duf- 
ferin,  Manitoba ;  Lake  Winnipeg !  Moose  Factory,  James  Bay ; 
Peace  River,  Athabaska !  Great  Slave  Lake  at  Fort  Resolution ! 
Balaena  Bay,  Newfoundland ! 

If  the  identification  writh  Say's  unfigured  ovalis  w^ere  beyond  dispute, 
the  latter  name  is  prior  and  would  have  to  be  adopted. 

Succinea  chrysis  Westerlund. 

Succinea  chrysis  Westerlund,  Nachrbl,  d.  D,  Mai.  Ges.,  1883,  p.  51  ;  Vega 
Expd.  Vetensk.  lakttag.,  iv,  p.  198,  pi.  iii,  fig.  10,  1885. 

Succinea  annexa  Westerlund,  Vega  Expd.,  p.  199,  pi.  m,  fig.  li,  1885. 

Succinea  chrysis  var.  aurelia  voN  Martens,  Conch.  Mitth.,  ll,  p.  184,  pi. 
XXXIII,  figs.  21-22,  1885. 

Succinea  lineata  W.  G.  Binney,  Man.  Am.  Landsh.,  app.,  p.  473,  fig.  515, 
1885,  not  5.  lineata  W.  G.  B.,  1857. 

Range.  —  Boreal  America  from  Greenland  to  Bering  Strait,  and  on 
the  opposite  shore  of  the  Strait. 

Greenland  (Posselt) ;  Fort  Simpson,  Mackenzie  River;  water- 
shed of  the  Yukon,  near  Dawson,  Yukon  Territory  !  30  miles  below 
the  Xanana  River  mouth  on  the  Yukon,  Alaska  !  the  Koyukuk  River, 
north  of  the  Yukon  !  Nulato  !  Andreafski !  and  the  Yukon  delta  !  Point 
Romanof !  shores  of  Norton  Sound  at  Egg  Island !  Besboro  Island ! 
Cape  Denbigh  !  Norton  Bay  !  Golofnin  Bay  !  Port  Clarence  !  Konyam 
Bay  on  the  Asiatic  shore  of  Bering  Strait ;  St.  Michael !  St. 
Mathew  !  St.  Paul !  and  St.  George  !  Islands,  Bering  Sea  ;  north  end 
of  Nunivak  Island !  the  Aleutian  chain !  Unalaska  !  Kadiak  Island ! 
Sitka  !  At  Chilkat  Inlet,  Alaska,  Krause  obtained  the  variety  aurelia 
von  Martens. 

This  is  the  commonest  and  largest  land  shell  of  the  boreal  American 
region,  passing  through  many  mutations,  but  easily  recognizable  in  all 
of  them  ;  often  with  a  rich  coloration  varying  from  olive  brown  to 
orange  and  usually  lineated  with  more  opaque  lighter  axial  streaks.  I 
do  not  regard  it  as  identical  with  the  S.  lineata  of  W.  G.  Binney, 
though  the  species  have  some  characters  in  common. 


Family  LYMN^IDiE. 

Genus  Lymnaea  Lamarck. 

Limnea    cochlea  Linn6,  Fauna   Svecica,    ed.    i,    pp.    374,    376,  1746  (not 

binomial). 
Vesica  {ex  parte)  Anonymous,  Mus.  Calon.,  p.  58,   1797  ;  Helix  stagnalis 

(and  amarula)  Linn6. 
Helix  (sp.)  LiNNi:,  Gmelin,  Bolten  in  Mus.  Bolt.,  p.  109,  1798. 


6o  LAND   AND    FRESH    WATER    MOLLUSKS 

Lymncea  Lamarck,  Prodr,  Nouv.  Clas.  Coq.,  p.   75,  1799  ;  Syst.  des  An.  s. 

Vert.,  p.  91,  1 80 1,  Helix  stagnalis  Linne. 
Litnneus  Draparnaud, Tableau,  pp.  30,  47,  1801,  no  type  cited  ;  Hist.,  pp. 

25,   28,  48,   1805. — GossE,  Nat.   Hist.   Moll.,  p.  86,    1854. —  Turton, 

Man.,  p.  127,  1 83 1,  type  L.  stagnalis  L. 

>  Galba  Schrank,  Fauna  Boica,  in,  pt.  2,  pp.   262,  285,  1803  ;  sole  ex.  L. 

truncatula  Miiller. 
Lytnncea  RoissY,   Hist.  Nat.  Moll.,  v,  p.   345,    1805.  —  Lamarck,   Encycl. 

Meth.,  pi.  459,  1816. — Schumacher,  Essai,  p.  199,  1817. — Lamarck, 

An.  s.  Vert.,  vi,  2,  p.  157,  1822. 
Lymnaus  Cuvier,  Regne  An.,  11,  p.  412,  1817. 
Lymnus  Montfort,  Conch.  Syst,  11,  p.  262,  18 10,  Z.  stagnalis  L. 
Lyinnea  Risso,    Hist.    Nat.   Eur.    Mer.,  iv,  p.  94,    1826  ;   ist  sp.  Z.  pereger 

(Miiller).     Not  Zjw«^a  Rafinesque,  Pw^i?^,  18 15. 
'^  Radix  Montfort,  Conch.    Syst.,    11,  p.    266,   1810.      Helix  auricularia 

Linne,  sole  ex.— Morch,  Vidensk.  Meddel.  Kjob.,  p.  302,  1864. 
Limnea  Fleming,  Hist.  Brit.  An.,  p.  273,  1828. 
Limnaa  Desmarest,  Rapp.,  Soc.  Philom.  Paris,  1812. —  Blainville,  Malac, 

I,  p.  448,  1825. —  Beck,  Index,  p.  no,  1838.  — Moquin  Tandon,  Hist., 

Nat.  Moll.  France,  11,  p.  458,  1855. 
Lymneus  Brard,  Hist,  des  Coq.  Terr,  et  Fluv.   Paris,  p.  133,  pi.  5,  181 5. — 

Say,  Joum.  Acad.  Nat.  Sci.  Phila.,-ii,  p.  167,  1821. 
^  Lymnula  Rafinesque,  Joum.  de  Phys.,  Lxxxviii,  p.  423,   1819  ;  =  Lym- 

nea  of  Authors,  fide  Rafinesque,  1.  c. 

>  Omphiscola  Rafinesque,  op.  cit.,  p.  423,  1819.     No  species  cited,  but  the 

only  Ohio  shell  corresponding  even  moderately  to  the  diagnosis  is  Z. 

reflex  a  Say. 
>•  Gulnaria  Leach,  Proofsheets,  pp.  146,  148,  18 19  \  fide  Turton,  Man.,  p. 

117,  1831.— Gray's  Turton,  p.  232,  1840.— Gray,  P.  Z.  S.,  1847,  p.  180  ; 

type  Z.  auricularia  (Linne). 
Stagnicola  Leach,  Proofsheets,  pp.  141,  145,  1819. — Jeffreys,  Linn.  Trans. 

XVI,  II,  p.  376,  May  29,  1830,  Z.  /a/«j/'m  Miiller. — Turton,  Man.,  pp. 

121-124,  Oct.,  1831. — Gray's  Turton,  pp.  237-242,  1840. — Gray,  P.  Z. 

S.,  1847,  p.    180;    no  type  cited. —  Leach,  Synops.  Moll.  Gt.  Brit.,  p. 

loi,  1852,  1st  sp.  Z.^/a^(fr (Miiller).     Not  Stagnicola  Brehm,  Aves,  Dec, 

1830. 
Auricularia  Fabricius,  Fortegnelse,  p.  94,  1823  (nude  name),  not  of  Blain- 
ville, 18 16. 

>  Omphiscola  Beck,  Index,  p.  no,  1838,  Z.  glabra  (Miiller). —  H.  and  A. 

Adams,  Gen.  Rec.  Moll.,  11,  p.  255,  1855  ;  not  Omphiscola  Raf.,  18 19. 
>Z/w«£»//^/^a  FiTziNGER,  Syst.  Verz.,  p.  112,  1833;  type  Z. /a/«5/m  (Miiller). 

—  Beck,  Index,  p.  no,  1838. — Morch,  Vidensk.  Medd.,p.  298,  1864. 
"^  Leptolitnnea   Swainson,   Malac,  p.   338,   1840;  Z.  elongata  Sowerby,  = 

Z.  ^/a^,?r  (Miiller). —  Morch,  Vidensk.  Meddel.  Kjob.,  p.  298,  1864. 
Adelina  Cantraine,  Mai.  Med.,  i,  p.  155,  1841  ;  type  4^.  elegans  Cantraine, 

not  Adelina  Chevrolat,  Coleopt.,    1833. 
Leachia  Jeffreys,   Linn.  Trans.,  xvi,   in,  p.  519,  1833,  not  of  Risso,  1829, 

or  Lesueur,  1821,  Z.  stagnalis  (Linne). 
";;>  Bulimnea  Haldeman,  Mon.  Limn.,  part  3,  p.  6,  July,  1841  ;  ^y^^^ Limnea 

megasoma  (Say)  Haldeman.     Not  of  H.  and  A.  Adams. 
'^  Acella  Haldeman.   Mon.   Limn.,  part  3,  p.  6,  July,   1841  ;  type  Limnea 

gracilis  (Say)  Haldeman. 
"^  Pleurolimncea  Meek,  Checkl.  N.  Am.  Fos.  Eocene,  pp.  9,  34.  1866  ;  Rep. 

Inv.  Foss.  Upper  Missouri,  p.  533,  1876  ;  type  P.  tenuicostata  Meek  and 

Hayden  (Eocene). 


FAMILY    LYMN^ID/E  6l 

~^  Polyrhytis  Meek,   Rep.   Inv.   Fos.   Upper  Missouri,  p.   532,    1876;    type 
Limnaa  kingi  Meek  (Pliocene). 

>  Omphtscola  Meek,    Rep.   Inv.   Fos.  Upper  Missouri,   p.   533,   1876  ;  type 

Limnaa  glabra  (Miiller)  ;  not  of  Rafinesque. 
Omphalia    "  Raf.,"    Meek,  op.   cit.,   p.   532,  in  syn. ;   err.  pro  Omphtscola 

Rafinesque. 
?  Erinna  H.   and  A.  Adams,  Gen.  Rec.   Moll.,   11,  p.  644,   1858;  type  E. 

newcombi  Adams. 
~y  Neritostoma  H.  and  A.  Adams,  Gen.  Rec.  Moll.,  n,  p.  253,  1855,  ist  sp. 

Z.  auricularia  (Linne).      Not  of  Morch,  1864. 
?  Vehitinopsis  Sandberger,  Land  u.  siissw.  Conch,   d.  Vorvvelt,  p.  700,  1875, 

type  Limncea  velutina  Desh.  (Lower  Pliocene). 

>  Leptolimnaus  Sandberger,  Land  u.  siissw.  Conch,  d.  Vorwelt,  p.   787, 

1875  ;  sole  ex.  cited  L.  glaber  (Miiller). 
Eulimneus  Sandberger,  Land  u.  sussw.   Conch,  d.   Vorwelt,  pp.   787,  844, 
1875  ;  sole  ex.  cited  L.  stagna/is  (L). 

>  i^t;5^arza  Westerlund,  Fauna,   Pal.   Reg.,  v,  p.  49,  1885  ;  L.  truncatula 

(Miiller)  ;  Acta  Soc.  Sci.  Slav,  Merid.,  CLi,  p.  118,  1902. 

>  Tanousta   Bourguignat,  in  Servain,    Hist.   Mai.  du  Lac  Balaton,    1881.^ 

Type  L.  zrmanjce  Brusina ;  Westerlund,  op.  cit.,  p.   53,   1885,  p.  118, 

1902. 
'^  Lymnophysa  (Fitzinger)  Hazay,  MaL  Blatt.,  2d  ser.,  iii,  p.  163,    1 881. 
^  Limnus  Dybowski,   Bull.   Imp.  Acad.  Sci.  St.  Petersburg,  xviii,  p.    113, 

March,  1903,  not  of  Agassiz,  nom.,  1847. 

>  Otnphalolimnus  Dybowski,  Nachrichtsbl.   d.   d.  Mai.   Ges.,   Sept.-Oct., 

1903,  XXXV,  p.  143,  1903.     Type  L.  lagorii  Dybowski ;  Bull.  Acad.  St. 

Petersb.,  xviii,  p.  113,  1903. 
'^  Physastra  Tapparone  Canefri,  Ann.  Mus.  Genov.,  xix,  p.   245,  1883. 

Type  P.  vestita  T.-C,  op.  cit.,  p.  246.     New  Guinea. 
^  Zagrabica  Brusina,  Beitr.  Pal.  Oest.-Ung.,    1884,  Z.  naticoides  Brus. — 

Westerlund,  Acta  Acad.  Sci.  Slav.  Merid.,  cli.,  p.  119,  1902. 
Not  Limncea  PoU,  Test.  Utr.   Sicil.,   i,  p.   31,    1791,    11,  p.   253,    1795  (not 

binomial). 

The  genus  Lymncea  as  now  understood  is  due  to  Lamarck,  though 
several  authors,  including  Westerlund  as  late  as  1885,  have  given 
credit  for  it  to  Bruguiere.  This  has  probably  arisen  from  a  failure  to 
observe  the  dates  of  the  different  livraisons  which  contained  the  plates 
of  the  Encyclopedie  Methodique.  The  plate  containing  the  name 
Lymncea  was  not  issued  until  1816  (though  often  cited  as  1791),  and 
then  it  was  under  the  supervision  of  Lamarck,  Bruguiere  having 
nothing  to  do  with  it.  The  name  Lymncea  had  already  been  used 
by  Poli,  in  1791?  for  the  animal  of  various  unrelated  bivalves,  but 
his  ingenious  quadrinominal  system  takes  the  work  of  Poli  out  of 
the  category  of  those  which  can  be  cited  in  nomenclature,  except 
historically. 

1  The  multitude  of  group  names  used  for  mutations  of  Lymncea  stagnalis  and 
other  species  by  Servain  in  his  '  Lake  Balaton '  paper,  can  hardly  be  regarded  as 
having  entered  into  systematic  nomenclature,  as  thej  are  groups  of  less  value 
than  species,  and  physiological  rather  than  hereditary,  according  to  Hazay. 


63  LAND    AND    FRESH    WATER    MOLLUSKS 

The  name  Lymncea  has  been  spelled  in  many  different  ways,  the 
most  correct  being  Litnncea^  but  there  seems  to  be  no  good  reason  for 
changing  the  original  form,  especially  as  no  derivation  was  given  by 
Lamarck.  The  Helix  stagnalis  of  Linne,  being  the  only  species 
mentioned,  necessarily  becomes  the  type. 

Four  years  after  Lamarck,  Schrank  gave  the  name  Galba  to  a 
species  which  was  without  doubt  the  Buccinum  truncatulum  of 
Miiller.  It  has  been  referred  to  B.  palustre  Miiller,  but  a  scrutiny  of 
the  very  careful  description  of  both  shell  and  animal  reveals  that  it 
agrees  with  no  local  species  of  the  group  except  a  young  iruncatula. 
A  little  later  Montfort  separated  the  L.  auricularia  group  under  the 
name  of  Radix^  and  in  1819  Rafinesque,  in  a  summary  of  the  forms 
collected  on  the  Ohio  River,  proposed  Omphiscola  for  species  which 
have  the  peristome  reflected  over  the  pillar  and  body  with  an  umbilical 
chink  between  the  reflection  and  the  body  of  the  shell.  He  cites  no 
species,  but  of  the  Ohio  species  only  L.  reflexa  Say  can  be  said  to 
agree  with  the  diagnosis.  This  character  is  however  of  minor  impor- 
tance. Rafinesque's  name  has  been  applied  to  several  European 
species  but  without  adequate  grounds,  since  there  is  no  species  of  the 
Radix  group  known  in  any  part  of  the  Ohio  system. 

The  name  Stagnicola  Leach  was  cited  in  synonymy  by  Jeffreys  in 
1830,  in  connection  with  L.  palustris  (Miiller) ,  thus  antedating  JLim- 
nophysa  Fitzinger,  1833,  based  on  the  same  type.  Stagnicola  was 
used  by  Brehm  for  a  bird  in  December,  1830,  but  Jeffreys'  paper  was 
issued  May  29.  Both  these  names  have  been  loosely  vised  in  the  lit- 
erature, but  must  be  restricted  to  the  typical  and  original  forms.  If 
the  columnar  species  like  L.  glaber  be  separated  in  a  section  by  them- 
selves, Leptolimnea  Swainson  appears  to  be  the  first  available  name. 
Erinna  Adams  is  a  Limnseid  modified  for  existence  on  rocks  in  rapid 
streams  and  waterfalls,  the  peristome  being  continued  over  the  body 
and  behind  the  broad  excavated  pillar,  and  the  spire  shortened,  so  that 
the  animal  may  cling  tightly  to  its  situs.  The  descriptions  of  this 
form  are  rather  misleading,  the  so-called  '  lamina '  being  merely  the 
pillar.  The  fossil  Velutinopsis  is  more  like  Choanomphalus  than 
Lymncea^  judging  by  the  figures.  The  description  of  Tanousia  reads 
as  if  it  was  founded  upon  an  abnormal  or  monstrous  specimen.  The 
reversed  physiform  Lymncea  of  the  South  Sea  Islands  will  be  included 
under  Physastra  Tapparone-Canefri ;  a  species  from  Hawaii  which 
is  dextral  but  may  be  otherwise  similar,  has  recently  been  shown  by 
Pilsbry  to  have  a  somewhat  different  radula  from  the  ordinary  Lym- 
ncea of  north  Europe  and  America. 


FAMILY    LYMN^ID.«  63 

Dybowski  has  recently  applied  the  name  Omphalolimnus  to  a 
species  of  Lyinncea  from  the  Crimea,  which  in  outline  resembles  L. 
stagnalis  var.  arenaria  Colbeau,  but  which  instead  of  having  the 
axis  pervious  and  the  pillar  gyrate,  as  in  most  species  of  this  type,  has 
the  subumbilicate  base  and  raised  inner  lip  of  the  Radix  section,  to 
which  his  L.  lagorii  probably  belongs,  although  it  has  a  more  ele- 
vated spire  than  most  of  the  species  of  this  section,  being  in  this  re- 
spect intermediate  between  the  latter  and  Lytnncea  proper. 

The  existence  of  fresh  water  shells  in  lakes  or  ponds  where  the 
water,  through  evaporation,  is  gradually  becoming  more  alkaline,  has 
been  shown  to  be  accompanied,  in  the  lake-beds  of  the  Great  Basin  of 
the  western  United  States,  by  a  tendency  to  solidification,  thickening 
and  corrugation  or  ribbing  of  the  shells,  regardless  of  their  systematic 
relations.  This  goes  on  until  the  alkalinity  becomes  so  great  that  mol- 
luscan  life  is  no  longer  possible.  We  find  in  the  fresh  water  Pliocene 
beds  of  Utah,  Lymncea^  Pompkolyx,  Carinifex^  Physa  and  Planorbis 
exhibiting  these  changes  as  we  ascend  in  the  beds,  until  the  latter  be- 
come barren  of  life.  To  these  modifications  we  probably  owe  such 
forms  as  Polyrhytis^  Pleurolimncea^  Vorticifex^  etc.  I  have  shown 
in  another  place^  how  such  factors  may  be  supposed  to  act  in  the  case 
of  land  shells  exposed  to  alkaline  dust  on  tropical  islands  such  as  the 
Galapagos.  While  such  changes  are  the  result  of  the  direct  action  of 
the  environment  on  the  individual,  and  not  hereditary  or  evolutionary, 
it  is  nevertheless  convenient  to  recognize  the  results  in  the  systematic 
arrangement  of  the  species. 

Disregarding  synonyms,  which  can  be  deduced  from  the  preceding 
data,  the  general  arrangement  of  the  groups  of  the  genus  Lymncea 
would  be  about  as  follows  : 

Subgenus  Lymnaea  s.  s. 

Section  Lymncea  s.  s.  Shell  thin,  with  an  acute  and  slender  spire 
and  expanded  last  whorl ;  the  axis  twisted,  forming  a  (usually  per- 
vious) spiral  coil  without  a  true  umbilicus  ;  the  callus  on  the  body 
closely  appressed ;  the  outer  lip  flaring  more  or  less,  simple,  sharp, 
normally  without  any  varical  thickening.  Type  L .  stagnalis  (Linn6) . 
Holarctic. 

Section  Bulimnea  Haldeman.  Shell  large  and  solid,  bulimiform, 
with  an  impervious  axis,  a  twisted  or  subplicate  pillar,  the  callus  on 
the  body  and  pillar  closely  appressed,  and  the  outer  lip  not  thickened 
or  expanded.     Type  Lymncea  megasoma  Say.     Nearctic. 

*  Proc.  Acad.  Nat.  Sciences  Phila.,  for  1896,  pp.  406-426. 


64  LAND    AND    FRESH    WATER    MOLLUSKS 

Section  Radix  Montfort.  Shell  thin,  usually  with  a  short  spire  and 
ample  last  whorl ;  the  axis  twisted  but  not  gyrate,  the  outer  lip  often 
expanded,  the  inner  one  more  or  less  elevated  and  continuous  across 
the  body,  forming  a  more  or  less  conspicuous  umbilicus  ;  the  outer  lip 
thin.     Type  Lymncea  auricularia  (Linn^) .     Holarctic. 

The  umbilicus  in  this  group  varies  from  a  mere  chink  to  a  rather 
large  orifice  through  which  a  bristle  may  be  passed  nearly  to  the  apex 
of  the  shell. 

Section  Cyclolimncea  Dall,  nov.  Shell  thin,  involute,  the  last  whorl 
as  long  as  the  shell,  the  outer  lip  thin,  simple,  not  expanded,  the  inner 
lip  appressed,  the  axis  not  plicate,  but  with  a  small  umbilical  chink. 
Type  LymtK^a  involuta  Harvey.  British.  The  mantle  is  said  to  be 
extended  partly  over  the  shell. 

Section  Polyrhytis  Meek.  Shell  like  Radix^  but  axially  strongly 
ribbed.     Type  Z.  i^/«^/ Meek.     Pliocene,  N.  Am. 

Section  Acella  Haldeman.  Shell  thin,  smooth,  acute,  extremely 
slender;  the  aperture  expanded  at  the  margin,  the  inner  lip  not 
appressed,  a  moderate  chink  behind  it,  the  axis  gyrate,  pervious, 
not  plicate;  the  outer  lip  simple,  sharp.  Type  L.  gracilis  Jay. 
Nearctic. 

Section  Pleurolimncea  Meek.  Shell  like  Acella^  but  axially  promi- 
nently ribbed.  Type  L.  tenuicostata  Meek  and  Hayden.  Eocene, 
N.  Am. 

Section  Galba  Schrank.  Shell  turrited,  the  whorls  gradually  in- 
creasing, smooth ;  the  last  whorl  not  inflated ;  the  aperture  moderate ; 
the  outer  lip  not  expanded  or  thickened  ;  the  inner  lip  not  appressed  ; 
the  pillar  not  twisted  or  plicate,  the  axis  minutely  umbilicate.  Type 
L.  truncatula  (Miiller).     Holarctic. 

Subgenus  Stagnicola  Leach. 

Section  Stagnicola  s.  s.  Shell  elongate,  smooth,  the  whorls  gradu- 
ally increasing,  the  last  whorl  moderate ;  the  outer  lip  sharp,  not  ex- 
panded, with  a  varical  thickening  within,  in  the  adult ;  the  pillar  dis- 
tinctly plicate,  the  inner  lip  appressed,  the  axis  slightly  or  not  at  all 
perforate.     Type  Z.. /a/^^/r/^  (Miiller).     Holarctic. 

Section  Leptolimnea  Swainson.  Shell  like  Stagnicola  but  more 
cylindrical,  with  numerous  whorls  and  a  small  aperture.  Type  L. 
glaber  (Muller).     Palearctic. 

?  Section  Physastra  Tapparone-Canefri.  Shell  like  Stagnicola  but 
with  a  coarse  dehiscent  periostracum  and  coiled  sinistrally.  Type  P. 
vestita  T.-C.     Polynesian. 


FAMILY    LYMN^ID^  65 

Genus  Erinna  Adams. 
Shell  small,  with  a  short  spire,  a  large  final  whorl ;   the  aperture 
with  a  continuous  peristome  wliich  passes  behind  a  broad  somewhat 
excavated  pillar ;    axis  imperforate  and  the  pillar  not  plicate.     Type 
E.  newcotnbi  Adams.     Hawaiian. 

IncertcB  sedis. 

Velutinofsis  Sandberger.  Shell  almost  planorboid,  with  few, 
rounded,  rapidly  increasing  whorls  ;  the  aperture  simple,  suborbicular, 
the  peristome  sharp,  simple,  not  reflected ;  the  pillar  lip  broad,  not 
appressed  ;  the  axis  umbilicate.  Type  Z.  velutina  Deshayes.  Plio- 
cene of  the  Crimea. 

Tanousia  Bourguignat.  Shell  small  ovate  conic,  closely  and  almost 
involutely  coiled ;  the  last  whorl  inflated,  subcarinate  behind,  the  aper- 
ture contracted.  Type  Z^.  zrmanjceBrusma..  Pleistocene  of  Dal matia. 
The  group  was  named  Sandria  by  Brusina  in  1S8 5  ^Jide  Westerlund. 

Zagrabica  Brusina.  Shell  ventricose,  with  a  short  acute  spire  and 
few  rounded  whorls,  rugose,  umbilicate,  the  last  whorl  ample,  with  a 
rotund  transverse  aperture,  and  continuous  peristome  appressed  on  the 
columellar  margin ;  the  outer  lip  simple.  The  type  is  a  Pleistocene 
fossil.  A  recent  form  from  the  Caspian  has  been  referred  to  this  group 
by  Dybowski,  under  the  name  of  Z.  brusiniana. 

I  have  not  seen  specimens,  but  the  description  reads  as  if  the  shell 
might  be  a  member  of  the  Radix  group  which  has  been  modified  by 
life  in  brackish  water. 

Lymnaea  stagnalis  Linn6. 

Helix  stagnalis  LiNi*6,  Syst.  Nat.,  ed.  x,  p.  774,  1758;  ed.  xii,  p.  1249, 
1767. 

Lymncea  stagnalis  Lamarck,  Prodr.,  p.  75,  1799. 

Lytnncea  jugularis  Say,  Art.  Conchology,  Nicholson's  Encyc,  i  (no  pagina- 
tion), 1817  ;  3d  ed.  (p.  6),  1819. — Haldeman,  Men.  limn.,  p.  16,  pi.  iv, 
1841. 

LymncEa  appressa  Say,  Joum.  Acad.  Nat.  Sci.,  Phila.,  ll,  p.  168,  1818. — 
Haldeman,  Mon.  Limn.,  p.  18,  pi.  v,  1842. 

IJmncea  stagnalis  W.  G.  Binney,  Land  and  Fw.  Sh.  N.  Am.,  11,  p.  25,  figs. 
28-32,  1865. 

Range.  —  Europe,  the  Caucasus,  western  and  northern  Asia,  the 
northern  United  States,  Canada  and  British  America. 

Lake  Superior,  Lake  Winnipeg  !  the  Saskatchewan  River  !  Carberry, 
Manitoba ;  Moose  Factory,  James  Bay  !  Knee  Lake,  Keewatin  !  Slave 
River,  25  miles  below  Peace  River !  Great  Slave  Lake  at  Fort  Rae  ! 
and  Fort  Resolution !  Fort  Simpson !  and  Fort  Smith !  on  the  Mac- 


66 


LAND    AND    FRESH    WATER    MOLLUSKS 


Fig.  42.  Lymncea 
stagnalis. 


kenzie  River ;  Fort  Anderson,  Lat.  68°  N. !  and  Lake  Harrison,  Lat. 

70°  N !  Shawnigan  Lake,  Vancouver  Island !  and  Dall  River,  Lat. 
66°  N. !  of  the  Yukon  drainage  in  Alaska.  The 
following  additional  localities  are  cited  from  the 
literature :  York  Factory,  Keewatin,  and  the  Nel- 
son River ;  Egg  Lake,  Alberta ;  Red  Deer,  McLeod, 
and  Olds  ;  Lake  Isle  Lacrosse  and  Vermilion  Lake  ; 
Lake  Osoyoos,  B.  C.  (but  replaced  west  of  the 
Cascades  by  L.  sumassii^  according  to  J.  K. 
Lord)  ;  Syniakwateen  Lake,  B.C.;  lakes  in  the 
Kenai  Peninsula,  Alaska  (Wossnessenski)  ;  Stewart 
River,  Yukon  district  (Canadian  Geol.  Survey). 

It  seems  unnecessary  to  cite  the  multitudinous 
varietal  names  bestowed  on  the  mutations  of  this 
species  in  Europe.  In  a  wide  sense  it  is  one  of  the 
most  easily  recognizable  of  fresh  water  shells,  as 
it  is  one  of  the  most  conspicuous  of  circumboreal 
species. 

Lymnaea  petersi  n.  sp.     Plate  11,  fig.  3. 

Shell  extremely  thin,  of  five  or  more  tumid  rapidly  enlarging  whorls  ; 
spire  acute,  the  suture  deep ;  whorls  rounded,  the  periphery  nearer 
the  preceding  suture ;  shell  of  a  blackish  brown,  polished,  finely 
sharply  spirally  striate ;  periostracum  brownish,  darker  at  resting 
stages ;  aperture  oval,  a  thin  wash  of  callus  on  the  body ;  pillar  very 
thin,  gyrate,  the  gyrations  pervious ;  the  outer  lip  not  thickened. 
Height  16;  max.  diam.  8;  height  of  aperture  8.5  ;  width  5.2  mm. 

Range.  —  Koyukuk  River,  north  of  the  Yukon  in  Alaska  ;  W.  J. 
Peters  of  the  U.  S.  Geological  Survey. 

This  very  delicate  and  pretty  species  appears  to  belong  to  the  typical 
Lymncea  in  spite  of  its  small  size ;  it  has  much  the  aspect  of  a  minute 
L.  randolfhi^  but  has  more  whorls  in  less  than  half  the  height,  and  is 
of  quite  a  different  color  and  without  angularity  to  the  whorls. 

Lymnaea  atkaensis  Dall.     Plate  11,  figs.  8,  10. 

Umncea  atkaensis  Dall,  Proc.  U.  S.  Nat.  Mus.,  vii,  p.  343,  1884. 

Range.  —  Lake  on  the  island  of  Atka,  Aleutian  chain,  near  Korovin 
Bay. 

Shell  with  about  four  ovate  whorls  rapidly  increasing,  of  a  dark 
olive  sometimes  purplish  tint,  very  thin,  malleated,  microscopically 
reticulated,  with  obscure  revolving  ridges ;  the  aperture  ovate,  not 
expanded,  the  margins  thin,  that  on  the  pillar  narrowly  reflected; 


(  UNIVERSITY 


FAMILY    LYMN^ID^ 


67 


pillar  gyrate,  pervious,  in  the  early  whorls  widely  so,  a  condition 
concealed  in  the  adult. 

This  form  grows  in  a  region  containing  little  lime,  and  the  shells 
are  extremely  thin  and  often  eroded  into  holes,  which  exhibit  the 
peculiarities  of  the  axis  by  which  the  species  is  relegated  to  the  typical 
Lymnaeas,  though  externally  it  has  much  the  appearance  of  a  small 
Radix.  The  species  has  been  figured  in  the  newer  portion  of  the 
Conchylien  Cabinet,  but  I  have  not  the  reference  at  hand. 

Adults  measure  : 


Height. 

Max.  Diam. 

Height  of  Aperture. 

Width. 

Whorls, 

26.5 

16.S 

16.5 

10.S 

4 

24.0 

13.0 

14.0 

9.a 

?>y^ 

17.0 

11.5 

11.2 

7-S 

^% 

*Lymnaea  lepida  Gould. 

Limncea  lepida  Gould,  Proc.  Boston  Soc.  Nat.  Hist.,  11,  p.  211,  1847  ;  Moll. 
U.    S.   Expl.  Exp.,  p.    121,   figs.    141,    \\\a,   1852. — 
BiNNEV,    Land  and  Fw.  Sh.  N.  Am.,  11,  p.  29,  fig.  33, 
1865. 

Range. — Lake  Vancouver,  Oregon  (Wilkes)  ;  near 
Cliallis,  Idaho  (Merriam)  ! 

A  species  existing  near  the  boundary  and  doubtless 
to  be  found  in  southern  British  Columbia. 


Fig.  43.  Lym- 
ntea  lepida 
Gould. 


♦Lymnaea  (Bulimnea)  megasoma  Say. 

Lymnaus  megasomusSw ,  Rep.  Long's  Exp.,  11,  p.  263,  pi.  xv,  fig.  10,  1824. — 
KiJSTER,  Conchy  Cab.,  ed.  11,  Limncea,  p.  36,  pi.  vi,  figs.  20,  21. 

Ldmnea  megasoma  Haldeman,  Mon.    Limn.,  p.  13,   pi. 

Ill,    figs.    1-3,    1841. — Whitfield,     Bull.     Am. 

Mus.  Nat.  Hist.  N.  Y.,  i.  No.  2,  p.  29,  pi.  v,  1882. 

Limncea  megastoma  Sowerby,  Conch.  Icon.,  xviii,  pi. 

II,  fig.  12,  1872. 
Limncea  megalosoma  Sandberger,  Conch,  d.  Urw.,   p. 
581,  1873- 


Range.— '^or^Q.m  New  England,  Canada  and 
British  America  to  Lat.  57°  N. 

Lake  Superior!  Vermilion  Lake,  H.  B.  T. ;   to 
Etchimamish  Lake,  in  Lat.  57°  between  the  Nel- 
FiG.  44.    Lymncea  son  River  and  the  Height  of   Land,  Keewatin; 
megasoma  Say.  Bois  Blanc  Lake,  Manitoba  ! 

The  British  American  localities  are  cited  from  the  literature,  and 
except  the  last  I  have  been  unable  to  verify  them  by  an  examination 
of  authentic  specimens. 


68  LAND    AND    FRESH    WATER   MOLLUSKS 

Lymnaea  (Radix)  mighelsi  Binney. 

JUmncea  decollata  Mighels,  Proc.  Boston  Soc.   Nat.  Hist.,  i,  p.  49,  1841. 

MiGHELS  and  Adams,  Boston  Journ.  Nat.  Hist.,  iv,  p.  336,  pi.  iv,  fig.  13 
(four  views),  1842. 

Limnea  catascopium.  Haldeman,  Mon.  Limn.,  p.  52,  1842  ;  not  of  Say. 

UmncEus  decollatus  Kuster,  Conch.  Cab.,  ed.  11,  Mon.  Limn.,  p.  45,  pL 
VIII,  figs.  11-14,  1862. 

LimncBa  ampla  Mighels,  Boston  Journ.  Nat.  Hist.,  iv,  p.  347,  pi.  xvi,  figs. 
\a-\c,  April,  1843  ;  not  of  Hartmann,  1842. — Binney,  Land  and  Fw. 
Sh.  N.  Am.,  II,  p.  30,  figs.  34-35,  1865. 

IJmncca  mighelsi,  W.  G.  Binney,  Land  aijd  Fw.  Sh.  N.  Am.,  11,  p.  31,  foot- 
note,   1865. 

Limncea  angulata  Sowerby,  Conch.  Icon. ,  xviii,  Mon.  LimncBa,  pi.  vii,  fig. 
47,  Dec,  1872. 

Limnaa  emarginata  Say,  var.  mighelsi  Binney,  Nylander,  Distr.  of  Limncea, 
etc.,  pis.  i-iv,  1 90 1. 

Range.  —  Aroostook  Co.,  Maine;  Province  of  Quebec;  northern 
Michigan .? 

Aroostook  Co.,  Maine !  Brome  Lake,  Province  of  Quebec !  Lake 
Namakan,  north  of  Lake  Superior,  western  Ontario ;  Lake  of  the 
Woods,  Manitoba. 

The  earliest  name  of  this  species  is  decollata.,  which  was  applied  to 
a  stunted  variety  living  in  acidulous  water  which  destroyed  the  early 
whorls.  This  name,  however,  being  quite  inapplicable  to  the  normal 
shell,  would  best  be  kept  for  the  shells  to  which  it  was 
applied,  and  retained  in  a  varietal  sense.  After  an 
examination  of  Say's  types  of  Z.  emarginata  I  am 
quite  confident,  as  species  go  in  Lymncea.,  that  it  is 
distinct  from  the  present  form,  which  I  have  never 
seen  from  the  Western  region.  This  species,  L. 
'  7  ■  ,  .  J  mighelsi.,  is  apparently  a  representative  of  Radix ^ 
while  the  thickening  of  the  outer  lip  internally  in 
X.  emarginata  var.  canadensis  leads  to  the  suspicion  that  it  is 
related  to  Stagnicola.  Owing  to  the  manner  in  which  various  forms 
of  emarginata  have  been  summarily  united  with  Z..  mighelsi  by  rep- 
utable students,  I  shall  on  the  present  occasion  waive  this  doubt  and 
proceed  to  its  immediate  consideration.  It  may,  however,  be  pointed 
out  that  W.  G.  Binney  seems  to  have  been  of  the  same  opinion  when, 
in  1865,  he  placed  L.  emarginata  in  the  same  group  as  L.  palustris. 

Lymnaea  (Stagnicola.?)  emarginata  Say. 

Lymneus  emarginatus  Say,  Journ.  Acad.  Nat.  Sci.  Phila.,  11,  p.  170,  1821  ; 

Long's  Exp.  Rep.,  11,  p.  263,  1824  (Maine). 
t Limneus  emarginattcs  Say,  Am.  Conch.,  vi,  pi.  55,  fig.  i,  1834. 
Limnetts  ontariensis  Muhlfeldt  in  Kuster,  \%(i2,  fide  W.  G.  Binney,  op.  ch., 

p.  52,  1865. 


FAMILY    LYMN^ID^  69 

Limnea  etnarginata  Haldeman,  Mon.  Limn.,  p.  10,  pi.  11,  figs.  4-5,  1841. 

f  Limnea  serrata  Haldeman,  Mon.  Limn.,  p.  12,  pi.  11,  fig.  7,  1841  (path- 
ologic specimen,  figure  copied  by  Binney,  op.  cit.,  p.  52,  fig.  78). 

Umncsa  sca/art's  WESTERhVUD,  Vega  Exp.  Vet.  lakt.,  iv,  p.  201,  pi.  iv,  fig. 
13,  1885.     Not  Z.  scalaris  A.  Braun,  1853,  or  Sowerby,  1872. 

Umnaa  canadensis  SowEKhY,  Conch.  Icon.,  xviii,  Mon.  IdmncBa,  pi.  vii,  figs. 
45,  a-b,  1872. 

Range.  —  Northern  United  States  east  of  the  Mississippi,  Canada, 
and  northwestward. 

Lakes  in  northern  Maine  (Say)  !  Lake  Champlain  and  Ontario; 
Crooked  Lake,  Emmet  Co.,  Michigan!  English  River,  Keewatin, 
Hudson  Bay!  Port  Clarence,  Alaska  (Vega  Expd.). 

After  considerable  study  I  have  been  forced  to  the 
conclusion  that  several  species  were  identified  under 
this  name  by  Say  himself,  as  well  as  others.  Say's 
figure  is  wretched  and  does  not  represent  the  typical 
form  from  Maine,  as  at  first  described.  The  latter  is 
apparently  represented  by  specimens  labelled  by  Say 
himself,  still  preserved  in  the  Academy  at  Philadel- 
phia, and  which  must  be  regarded  as  typical.  The  F^°-  46-  Lym- 
shell  is  small,  with  an  acute  spire  ;  one  of  the  specimens  *^°'  ^'"^''^"^  * 
has  the  suture  deeply  impressed,  but  not  the  others, 
which  seem  more  normal.  Westerlund's  figure  fairly  represents  the 
species;  Sowerby's  L.  canadensis^  judging  from  specimens  com- 
pared with  the  types  by  Mr.  E.  A.  Smith  of  the  British  Museum,  is 
probably  the  same,  though  the  shells  are  heavier  and  larger,  with  the 
lip  thickened  internally,  and  a  marked  umbilicus.  I  should  not,  in 
default  of  this  comparison  and  if  obliged  to  depend  on  Sowerby's 
figures,  have  felt  justified  in  uniting  them. 

Lymnaea  (Radix)  binneyi  Tryon. 

Linincea  binneyi  Tryon,  Am.  Journ.  Conch.,  I,  p.  229,  pi.  xxiil,  fig.  3,  1865 

(Hellgate  River,  Oregon). 
Limnaa  ampia  Trvon,  Mon,  Freshw.  Univ.  Moll.,  part  ll,  p.  91,  1872,  ex 

parte,  not  of  Mighels. 

Range.  —  Northern  United  States  west  of  Lake  Huron  and  the 
adjacent  British  possessions. 

Lake  Higgins,  southern  Michigan  !  Lake  Houghton,  northern  Mich- 
igan !  east  of  Fort  Colville,  Wash.  !  Fort  Vancouver,  Columbia  River  ! 
Sumas  Prairie,  B.  C. !  Vancouver  Island ;  Clear  Lake,  Athabaska, 
N.  Lat.  56°  !  Lake  Isle  Lacrosse,  Athabaska  !  English  River,  Manitoba  ! 

This  species  appears  to  be  quite  recognizable  but  has  been  frequently 
distributed  under  the  name  of  Z.  sumassi  or  ampla^  with  the  latter  of 


70  LAND   AND    FRESH    WATER    MOLLUSKS 

which  Tryon  himself  at  one  time  confounded  it.  It  has  a  short  spire 
with  appressed  or  moderately  conspicuous  suture,  ovate  form,  tumid 
whorls,  pale  color,  well  marked  umbilicus,  and  fine  spiral  striation. 
The  largest  specimen  I  have  seen  measured  27  mm.  high  and  18  mm. 
in  maximum  diameter ;  but  the  average  adult  is  about  24  x  15  mm.  I 
have  not  seen  any  specimens  angulated  at  the  shoulder. 

Lymnaea  (binneyi  var. ?)  preblei  Dall,  nov.    Plate  i,  figs,  i,  2. 

A  shell  which  when  young  is  almost  identical  with  L.  binneyi^  and 
which  may  prove  merely  a  giant  growth  of  it,  occurs  in  the  Hudson 
Bay  drainage.  When  full  grown  it  has  six  whorls,  with  much  the 
same  contour  as  Bulimnea  megasoma^  the  last  whorl  being  much  the 
largest,  moderately  expanded,  and  somewhat  produced  in  front.  The 
umbilicus  is  deep  and  partly  hidden  by  the  reflected  pillar  lip,  which 
is  continuous  and  more  or  less  raised  across  the  body.  There  is  no 
fold  on  the  pillar.  The  surface,  when  in  perfect  condition,  is  minutely 
but  sharply  sagrinate  by  the  intersection  of  axial  and  spiral  striae,  and 
is  often  malleate  besides.  The  shell  is  nearly  white  or  pale  straw 
color. 

Adults  measure : 


Whorls. 

Height. 

Max.  Diam. 

Height  of  aperture. 

Diam. 

6 

37 

23 

22.5 

13  mm. 

5.5 

38 

26 

26 

19     " 

Range.  —  English  River,  Manitoba  (Kennicott)  !  Knee  Lake,  Kee- 
watin  (E.  A.  Preble)  ! 

This  form  is  remarkable  for  its  size,  its  surface,  and  its  deep  umbil- 
icus. The  resemblance  of  its  profile  to  that  of  L.  megasoma  is  so 
marked  that  one  wonders  whether  some  of  the  records  of  the  latter  spe- 
cies from  high  northern  localities  may  not  have  been 
based  on  specimens  of  this  form.  They  are  easily 
separated,  however,  if  one  pays  attention  to  the  other 
characters,  and  the  present  form  probably  never  at- 
tains the  solidity  and  rich  coloration  so  characteristic 
of  megasoma. 

Fig. 47.  Lym-    Lymnaea  (Radix?)  colttmella  Say. 
ncBu  columella.        Ly^^cea  columella  Say.  Joum.  Acad.  Nat.  Sci.  Phila.,  I,  p. 

14,  1817. 
Lymnaus  columellus  Sa.\,  Journ.  Acad.  Nat.  Sci.  Phila,,  11,  p.  167,  1821. 
JUmnea  columella  Haldeman,  Mon.  Limn.,  p.  38,  pi.  xii,  figs.  13-15,  1842. 
— BiNNEY,  Land  and  Fw.  Sh.  N.  Am.,  n,  p.  32  {ex parte),  fig.  38,  1865, 


FAMILY    LYMN^ID^  7 1 

Range.  —  Manitoba  to  New  England,  New  Mexico,  and  Georgia. 

Lake  Superior  !  Lake  Winnipeg  (Rich)  ! 

This  attractive  species  is  readily  recognized  by  its  Succinea-Viik&  form 
and  fine  spiral  sculpture.  The  synonymy  as  given  by  Binney  and  others 
seems  to  need  revision.  I  am  not  of  the  opinion  that  this  form  belongs 
properly  in  the  Radix  group,  as  it  has  several  features  in  common 
with  Stagnicola^  notwithstanding  the  form  of  the  shell.  An  anatomi- 
cal examination  will  decide  the  question. 

Lymnaea  (Radix)  randolphi  F.  C.  Baker,  Plate  i,  figs.  3,  4. 
Lymnaa  randolphi  Baker,  Nautilus,  xviii.  No.  6,  p.  63,  Oct.,  1904. 

Shell  large,  thin,  angulate  or  subangulate  at  the  shoulder ;  constricted 
strongly  at  the  suture,  narrowly  and  deeply  umbilicate,  whorls  about 
four,  rapidly  increasing  in  size  but  frequently  decollate ;  when  entire 
the  spire  is  less  in  length  than  the  aperture  but  the  proportion  is  vari- 
able ;  in  conformity  with  the  sutural  constriction  the  posterior  angle  of 
the  aperture  is  usually  somewhat  narrow,  the  apertural  margin  con- 
tinuous over  the  body,  with  a  narrow  deep  umbilicus  over  which  the 
pillar  lip  may  be  reflected.  The  pillar  is  sometimes  slightly  sinuous 
but  not  plicate,  the  surface  may  be  smooth  and  polished,  malleated, 
spirally  threaded  or  minutely  reticulated  by  axial  and  spiral  lines. 
The  periostracum  is  pale,  but  usually  has  a  dark  line  at  resting  stages  ; 
the  outer  lip  is  hardly  expanded  though  often  a  little  patulous  in  front ; 
it  is  never  internally  thickened.     Measurements  : 


l^borls. 

Height. 

Max.  Diam. 

Height  of  aperture. 

Width. 

3-5 

31 

19 

18 

ii.o  mm, 

4 

41 

23 

34 

15-5     " 

4 

35 

27 

24 

15-6    " 

Range.  —  Lake  near  Cosmos  River,  north  of  the  Kowak  River, 
Alaska,  about  N.  Lat.  68°  (Lieutenant  Stoney)  !  Kowak  River,  Alaska 
(Stoney)  !  Nushagak  River,  Alaska  !  Lake  Marsh!  and  Lake  Linde- 
man,  Yukon  Territory  !  Lake  La  Hoclie,  British  Columbia  !  East  of 
Fort  Colville,  Wash.  ! 

This  form  is  very  recognizable,  with  its  angular  whorls  and  deeply 
constricted  suture.  A  specimen  from  near  Fort  Colville,  figured  by 
Binney  as  a  possible  variety  of  L.  sumassi  Baird  {op.  cit..,  p.  43,  fig. 
58) ,  may  prove  a  feebly  angulated  and  unusually  short  spired  specimen 
of  this  species.  I  have  received  it  under  the  names  ampla.,  sumassi.,  etc., 
from  several  Pacific  Coast  correspondents,  and  a  large  number  of  mostly 
defective  specimens  were  obtained  by  the  expedition  into  northwestern 


72  LAND    AND    FRESH    WATER    MOLLUSKS 

Alaska  commanded  by  Lieutenant  Stoney,  U.  S.  N.  The  true  Z. 
sumassi  Baird  is  apparently  a  Stagnicola^  but  the  present  species 
belongs  to  Radix.  It  is  not  in  the  least  like  Z.  mighelsi  {ampla 
Mighels)  though  often  given  that  name. 

Lymnaea  (Acella?)  kirtlandiana  Lea. 

f  JJmnaa  exilis  Lea,  Trans.  Am.  Phil.  Soc,  v,  p.  114,  pi,  xix,  fig.  82,  1837. 

Ohio. 
Limncea  kirtlandiana  Lea,  Proc.    Am.   Phil.   Soc,   11,  p.  33,   1841  ;  Trans. 

Am.  Phil.  Soc,  ix,  p.  12,  1842.  —  Binney,  Land  and  Fw.  Sh.  N.  Am., 

11,  p.  67,  1865. 
Limncea  lanceaia  Gould,    Proc.   Boston  Soc.   N.   Hist,   in,  p.  64,  1848. — 

Agassiz,  Lake  Superior,  p.  244,  pi.  vii,  figs.  8,  9,  1850.  — Tryon,  Mon. 

Limn.,  pt,  2,  pp.  112-113,  pi.  xviii,  figs,  10,  11,  1872. 

Range.  —  Ohio  to  Nebraska,  and  northward. 

Poland,  Ohio  !  Iowa  River,  Iowa  !  Apple  Creek,  Nebraska  !  Pic 
Lake,  north  of  Lake  Superior,  in  western  Ontario  ! 

The  original  types  of  Lea's  Limncea  exilis  are  in 
the  National  Museum,  and  after  a  careful  examina- 
tion of  them  I  am  inclined  to  believe  that  they  are 
somewhat  abnormal  dead  specimens  of  this  species 
rather  than  a  mutation  of  Z.  rejlexa^  as  supposed  by 
Binney;  unless  we   extend  Z.   rejlexa  to   cover  the 

'{..'.,      ,.      whole  group,  which  seems  to  me  unwarranted.     Z. 
ncBa     ktrtlandt-  .  . 

ana  Lea.  lanceata  is  an  immature  specimen  of  what  was  earlier 

called  kirtlandiana  by  Lea.  The  figures  of  both 
these  forms  in  Binney 's  work  are  uncharacteristic,  especially  that  of 
lanceata.,  which  shows  nothing  of  the  "  flatness  of  its  whorls  "  re- 
ferred to  by  Gould  in  his  remarks. 

These  shells  have  all  the  characteristics  of  Acella  except  that  they 
are  less  fragile,  larger,  and  darker  colored.  They  have  the  gyrate 
pillar  of  Lymncea  and  not  the  plicate  columella  of  Stagnicola.,  which 
in  other  respects  they  recall.  Until  an  exhaustive  anatomical  and 
experimental  study  of  these  animals  is  made,  all  group-references  must 
be  merely  tentative. 

Lymnaea  (Galba)  truncatula  Muller. 

Buccinum  truncatulum  Muller,   Verm.   Terr,  at   Fluv.,    11,   p.  130.    ^774 

(Europe). 
Limneus  minutus  Draparnaud,  Tableau,  p.  51,  1801  ;  Hist.,  p.  53>  pl-  i^^ 

figs.  5-6,  1805  (France). 
Limnaa  ferruginea  Haldeman,  Mon.  Limn.,  pt.  3,  third  page  of  cover,  Mar. 

13,  1 841  ;  pt.  4,  p.  49,  pi.  13,  figs.  19,  20,  1842  (Oregon). 

Range.  —  Europe,  northern  Asia  and  America. 


FAMILY    LYMN^ID^  73 

Bering    Id.,    Commander   Islands,    Bering    Sea!    Kadiak   Island, 
Alaska !  ponds  near  Yakutat  Bay,  Alaska  (Kincaid)  !  Fort  Simpson, 
Mackenzie  River  (Kennicott)  !  near  Brandon,  Manitoba  (Christy)  ! 
Oregon  (Nuttall)  ;  Hannah  Bay  (out  of  James  Bay) 
near  Moose  Factory  !  A 

Specimens  absolutely  identical  with  those  from  Eu-  «^ 

rope  have  been  collected  from  the  indicated  localities.  ^ 

It  is  quite  likely  that  some  of  the  specimens  reported        ^^°'  49-  Lym- 

by  collectors  under  the  name  of  humilis  or  desidiosa     "J^^,,    '^"f^ 

1         11  1        1  •  •  r^,      ,  ,,    ,     Miiller.    (Euro- 

may  have  belonged  to  this  species.     The  form  called     pean  specimen. ) 

ferruginea  by    Haldeman  seems  to  differ   only   by 
having  the  pillar  lip  more  closely  appressed,  a  character  w^hich  any 
large  series  will  show  to  be  inconstant  in  individuals  among  them- 
selves as  well  as  in  the  same  individual  in  different  stages. 

Lymnaea  (Galba)  humilis  Say. 

Lymneus  hionilis  Say,  Joum.  Acad.  Nat.   Sci.  Phila.,  ii,  p.  378,  1822  (South 

Carolina). 
Limnea  humilis  (Sxy)  Haldeman,  Mon.  Limn.,  p,  41,  pi.   13,  fig.   i,  1842 
(syn.  exclus.). — Binney,  Land  and  Fw.  Sh.  N,  Am., 
II,  p.  63,  fig.  99,  1865. 

Range. — From  Georgia  and  Kansas  northward. 
Lake  Superior  ;  Lake  Winnipeg ;  Brandon  ;  and  Pem- 
bina Mt.,  Manitoba. 

*,'.,.  I  have  been  unable  to  examine  any  authentic  speci- 

ncea     hu  milts  ^  i^ 

Say.  (Typical.)     ^nens  from  north  of  Lat.  49**,  and  the  above  localities 
are  cited  from  the  literature. 

Lymnaea  (Galba)  desidiosa  Say. 

Lymneus  desidiosus   Say,  Joum.    Acad.   Nat.   Sci.  Phila.,   11,  p.    169,    1821 

(Cayuga  Lake,  N.  Y.). 
Limneus  desidiosus  Say,  Am.  Conch.,  vi,  pi,  55,   fig.   3,  a 

1834.  /(ft 

Limnea    desidiosa  Haldeman,  Mon.   Limn.,  p.   31,  pi.  x,  \n\ 

1842  {ex parte). — Binney,  Land  and  Fw.  Sh.  N.  Am.,  \_y 

II,  p.  49,  fig.  68,  1865.  Fig.  51.  Lym- 

Range  — Northern  United  States  and  northward,     naea desidiosa 
Red  Deer  and  McLeod,  Alberta.    Lower  Saskatch-     '^o^^^^^a)  Say. 
ewan  near   Lake  Winnipeg ;    Brandon ;    Manitoba.     Osoyoos  Lake, 
British  Columbia  (J.  K.  Lord  fide  P.  P.  Carpenter) . 
The  above  localities  are  cited  from  the  literature. 

Lymnaea  (Galba)  galbana  Say. 

Lymneus  galbanus  Say,  Joum.  Acad,  Nat.  Sci.  Phila.,  v,  p.  123,  1825  (New 
Jersey  Pleistocene). 


74  LAND    AND    FRESH    WATKR    MOLLUSKS 

Umnea  galbana   Haldeman,    Mon.    Limn.,  p.    51,    pi.  xiii,  figs.   22,   23, 

1842. 
Limncea  philadelphica  Lea,  Proc.  Am.   Phil.  Soc,  11,  p.   32,    1841  ;  Trans. 

Am.   Phil.   Soc,  ix,  p.  8,  1844. —  Binney,  Land  and  Fw.  Sh.  N.  Am., 

II,  p.  50,  fig.  71,  1865.     (Philadelphia,  Pa.) 
LimncEa  traskiTKYO'H,  Proc.  Acad.  Nat.  Sci.   Phila.,  for  1863,  p.  149,  pi.    i, 

fig.  13,  1863. — Binney,  Land  and  Fw.   Sh.   N.  Am.,  11,  p.  60,  fig.  94, 

1865. — Tryon,  Mon.  Limn.,  p.  119,  pi.  17,  fig.  3  (not  p.  96,  nor  fig.  2), 

1872.     (Mountain  Lake,  near  San  Francisco,  Calif.)    Not  L.  iraskii  hea., 

1864,  nor  L.  proxima  Lea,  1856. 

Range.  —  Pleistocene  marls  of  Franklin,  New  Jer- 
sey ;  of  Anticosti  Island  !  of  Ottawa,  Canada  !  and  of 
the  left  bank  of  the  Yukon  River,  Alaska,  below  old 
Fort  Yukon !  Recent,  at  the  Grand  Rapids  of  the 
Saskatchewan  River,  near  Lake  Winnipeg  !     Grind- 

*  stone  Creek,  Nebraska!  Centre  City,   Pennsylvania! 

naa    galbana  '  _  •' '  •' 

Say  var.  phila-     Vancouver,    Columbia    River !    and   near   Monterey, 

delphica  Lea.  California !    Alaska    (von    Martens)  ;    Attawapiskat 

River,  S.  E.  Keewatin  !  (Mclnnes). 

This  small  species  has  the  spire  acute  and  short,  the  last  whorl  dis- 
proportionately swollen  and  usually  shouldered.  It  appears  to  have 
flourished  during  the  melting  of  the  glacial  ice,  and  to  the  muddy 
waters  of  the  period  its  peculiarities  may  be  due.  The  recent  form 
seems  less  abnormal  on  the  average. 

There  are  two  species  which  have  been  called  traskii — the  pres- 
ent one,  with  which  Tryon  afterward  mistakenly  united  L.  proxima 
Lea,  a  much  larger  species  ;  and  L.  traskii  Lea,  later 
called  tryoni  and  tryoniana  by  Dr.  Lea,  which  is  a 
Stagnicola. 

Lymnaea  (Galba)  holboUi  (Beck)  Moller.  y\g.  53.  Lym- 

Limnaa  {Limnophysa)  holbolli  Beck,  Index,  p.  1 11,  1838  ;     ncea  holbolli. 

nude  name.     Greenland. 
Lymncea  holbolli  MoiA.'E.v.,  Index,  Moll.  Gronl.,  p.  5,  1842. 
Limncea  holbolli  Morch,  Am.  Journ.  Conch.,  iv,  p.  36,  pi.  iv,  fig.  8,  1868. 

Range. — Godhaab,  Greenland. 

This  has  the  appearance  of  a  large  Z.  truncatula^  but  may  be  merely 
a  depauperate  variety  of  the  next  species. 

Lymnaea  (Galba)  vahlii  (Beck)  Moller. 

Limncea   {Umnophysa)   vahlii  Beck,    Index,    p.    iii,    1838;   nude  name. 

Greenland. 
Limncea  vahlii  MohL.'EK,  Index,  Moll.  Gronl.,  p.  4,  1842. 
Limncea  {Limnophysa)  vahlii  MoRCH,  Am.  Journ.  Conch.,  iv,  p.   34,  pi.   iv, 

figs.  1-7,  1868. 


FAMILY    L,YMN-«ID^  75 

Umncsa  {Limnopkysa)  senegalensts 'Rkc^,  Index,  p.  ill,  1838  (nude  name), 

Jide  MoRCH,  op.  cit.,  p.  35,  footnote. 
Liynncea  gronlandica  (Beck,    MS.)  Jay,   Cat.  Coll.,  1850,  p.  269,  No.  6298. 

—  MoRCH,  op.  cit.,  p.  33. 

Limncea  molleri  Beck,  Naturf.  Vers.  Kiel,  p.  123,  No.  4,  nude  name. — Gerst- 
FELDT,  Land  and  Sussw.  Conch.  Sibiriens,  p.  37,  1859. 

Lytnnaa pingelii  {^y.cyC)  Moller,  Index  Moll.  Gr6nl.,p.  5,  1842.  —  Morch, 
Am.  Joum.  Conch.,  iv,  o.  35,  1868,  et  vars.  nitida  et  solidula  et  malleata 
Morch,  /.  c. 

LymncEa  worftiskioldi  Beck,  Naturf,  Vers.,  Kiel,  p.  123,  No.  7,  nude  name. 

—  Morch,  Am.  Joum.  Conch.,  iv,  p.  35,  pi.  iv,  fig.  6,  1868. 
Limnaa  vahlii  var.  leucostoma  Morch,  Prod.  MoU.  Gronl.,  p.  4,  No.  11  /3; 

also  var.  »/z«tfr  Morch,  Am,  Joum.  Conch.,  iv,  p.  34,  1868. 
UmncEa  vahlii  var.  elongata  Moller  (MS.),  in  Morch,  Am.  Joum.  Conch., 

IV,  p.  40,  pi.  IV,  fig.  I,  1868. 
Limncea  arctica  Lea,  Joum.  Acad,  Nat,  Sci.  Phila.,  vi,  p.  160,  pi.  xxiv,  fig. 

75,  1866.     Hudson  Bay, 

Range.  —  Greenland  to  Alaska  and  south  to  Minnesota  and  British 
Columbia. 

Ft.  Resolution !  and  Ft.  Rae,  Great  Slave  Lake  !  Moose  River,  at 
Moose  Factory,  Hudson  Bay  !  Greenland  (many  localities)  !  Ungava, 
Labrador!    Weatoga,  Canada!    Minnesota  (Lapham)  !  Stewart  and 


Fig.  54.     Lymnesa  vaklii'i/lbVLer.  Fig.  55,     Lymncea  vahlii  v^x.  pingelii 

(Typical.)  Moller. 

Dall  Rivers,  north  of  the  Yukon,  Alaska !  St.  Michaels,  Norton 
Sound,  Alaska  I  headwaters  of  the  Yukon  in  Lakes  Bennett,  Marsh, 
and  Lindeman !  Loring,  Southeastern  Alaska,  on  Behm  Canal  ! 
Shawnigan  Lake,  British  Columbia !  Headwaters  of  the  Liard 
River  in  Lakes  Finlayson  and  Frances  !  Hannah  Bay  near  Moose 
Factory  ! 

Making  the  usual  allowances  for  variation,  this  is  a  fairly  well  dis- 
criminated species,  which  frequently  has  been  identified  as  L.  desidi- 
osa^  palusirts^  etc.  The  largest  are  more  fragile,  smaller  and  paler 
than  L.  palustris.,  and  not  especially  similar  to  it.  I  have  had  the 
advantage  of  being  able  to  consult  a  very  large  series  of  authentically 
named  Greenland  shells,  received  from  Morch  and  others,  as  well  as 
the  fine  Arctic  series  in  the  National  Museum.  Most  of  the  specimens 
are  microscopically  wrinkled  on  the  surface,  like  Z.  palustris.,  but 
this  character  is  not  absolutely  constant. 


76 


LAND    AND    FRESH   WATER    MOLLUSKS 


Lymnaea  (Stagnicola)  palustris  Muller. 

Buccinum palusire  yiviA.K¥i,YGxva..  Terr.,  li,  p.  131,  1774. 

Limneus palustris  Drap.,  Hist.,  p.  52,  pi.  11,  figs.  40-42,  iii,  figs.  1-2,  1805. 

Stagnicola  communis  Leach,  in  Jeffreys,  Linn.  Trans.,  xvi,  11,  p.  376,  1830. 

RossMASSLER,  Icon.,  I,  p.  96,   figs.   51,   52,  1835. —  TuRTON,  Man.,  p. 

121,  1831. —  Gray's   Turton,    p.    237,   1840.— Leach,  Syn.   Moll,  Gt. 

Brit.,  p.  103,  1852. 
Umnceus  elodes  Say,  Journ.  Acad.  Nat.   Sci.   Phila.,  11,  p.   169,  1821  ;  Am. 

Conch.,  IV,  pi.  XXXI,  fig.  3,  1832. 
JJmncea  elodes  GovLV>,  Inv.  Mass.,  p.  221,  figs.  146-7,  1841. 


Fig.  56,  a-f.      Lytnncea palustris  Muller  vars.      Fig.  56,^.     var.  rozvelli  hea 
from  Pacific  Coast. 


Limnea  fragilis  Haldeman,  Mon.  Limn.,  p.  20,  pi.   vi,  pi.  xv,  fig.  i,  1842  ; 

not  of  Linne. 
Umncea  nuttalliana  Lea,   Proc.  Am.   Phil,   Soc,  11,  p.   33,  1841. —  Binney, 

Land  and  Fw.  Sh.  N.  Am.,  11,  p.  45,  fig.  6,  1865. 
Limnea  ^^/a«^a Haldeman,  Mon.  Limn.,  p.  29,  pi.  ix,  figs.  6-8,  1842  (patho- 
logic mutation). 
Limncea  hay deni 'Lea,  Proc.  Acad.   Nat.  Sci.  Phila.,  p.  166,  1858. —  Binney, 
op.  cit.,  p.  44,  fig.  59,  1865  (pathologic  mutation). 

Limncea  plebeia  Gould  (nude  name),  in  Adams,  Am.  Journ. 

Sci.,  XL,  p.  268. 
Limncea proxima  Lea,  Proc.  Acad.  Nat.  Sci.  Phila.,  viii,  p. 
80,  1856. —  Binney,  op.  cit.,  p.  48,  fig.  67,  1865. 

Range. —  Circumboreal.     Northern  United  States 
and  Canada. 

Manitoba  :  Lake  Winnipeg  ;  Saskatchewan  River  ! 
Lake  of  the  Woods  ;  Red  River  of  the  North  !  Pem- 
bina ;  Turtle  Mt. ;  Carberry.  York  Factory  !  Kee- 
v^ratin.  Ungava  !  Labrador.  Alberta  :  Laggan  ;  Egg 
Lake;  Red  Deer;  McLeod;  Olds.  English  River, 
Keewatin  !  Moose  Factory,  Keew^atin  ;  Slave  River, 
25  miles  belowr  Peace  River !  Great  Slave  Lake  at 
Fort  Resolution !  Fort  Smith,  Mackenzie  River  I  Upper  Mackenzie 
River  !  Great  Bear  Lake  ;  Anticosti  Island  ;  Cypress  Hills  !  Assiniboia. 


Fig,  57.  Lynt- 
itcea  palustris 
var.  nuttalliana . 


FAMILY    LYMN^ID^  77 

California  !  Oregon  !  Seattle,  Wash. !  Sumas  Lake,  British  Colum- 
bia ;  Vancouver  Island !  headwaters  of  the  Yukon !  Lake  Marsh ! 
Lake  Lindeman  !  Old  Fort  Yukon,  Alaska  !  Saccatalontan  and  Nu- 
lato  !  Lower  Yukon,  and  in  the  Yukon  delta  !  Dall  River !  north  of  the 
Yukon  in  Alaska.  Point  Romanof ,  Norton  Sound,  Alaska  !  Avacha 
Bay,  Kamchatka  !  etc. 

This  well  known  species  is  almost  universally  distributed  in  the 
quiet  waters  of  boreal  America,  and  in  the  Pleistocene  marls.  The 
distinctions  which  have  been  relied  on  to  separate  L.  hay  dent  Lea, 
and  L.  expansa  Haldeman,  are  due  to  pathologic  mutations.  L. 
nuttalliana  and  proxima  Lea,  are  trivial  varieties. 

Lymnaea  (Stagnicola)  refleza  Say. 

Lytnneus  reflexus  Say,  Joum.  Acad.   Nat.  Sci.  Phila.,  li,  p.  167,  1821  ;  Am. 

Conch.,  IV,  pi.  XXXI,  fig.  2,  1832  (Lakes  Erie  and  Superior). 
Limneus  elongatus  Say,  Joum.  Acad.   Nat.  Sci.  Phila.,  ll, 

p.  167,  1821  ;  not  of  Draparnaud,  1805. 
Umneus  umbrosus  Say,  Am.   Conch.,    iv,  pi.   31,   fig.   1, 

1832  (new  name  for  elongatus  Say). 
Limncsa  exilis  Lea,  Trans.  Am.   Phil.  Soc,  v,  p.  114,  pi. 

XIX,  fig.  82,  1837  (pathologic  mutation). 

Range.  —  Northern  United  States  and  Canada. 

Prairie  Lake,  near  Red  River  of  the  North ;  and 

Beaver  Creek,  Manitoba. 

This  species  barely  crosses  the  boundary  and  may 

be  one  of  those  captured  by  the  northward  drainage  '  I  .  ^ 

'^  •'  ,  .  .      "        ntea  rejtexa  Say. 

when  the  headwaters  of  the  Mississippi  were  inter- 
rupted and  turned  northward  by  the  changes  in  the  land  levels  of  this 
region   which   have    been    elucidated    by   the   late   General    G.   K. 
Warren. 

Lymnaea  (Stagnicola)  catascopium  Say. 

Lyfnncea  catascopium  Say,  Nicholson's  Encycl.,  Am.  ed.,  11  (no  pagination), 

pi.  2,  fig   3,  181 7  (Delaware  River). 
Lymnceus  catascopium  Say ,  Am.  Conch.,  vi,  pi.  55,  fig.  2,  1832. 
Lymnea  cornea  Valenciennes,  in  Humboldt  and  Bonpland,  Rec.  d'obs.  de 

Zool.,  II,  p.  251,  1832. 
Limncea  sumassi  Baird,  Proc.  Zool.  Soc.   London,  1863,  p.  68. — Binney, 

Land  and  Fw.  Sh.  N.  Am.,  11,  p.  43,  fig.  57  (not  fig.  56),  1865  (British 

Columbia). 

Range.  —  Z.  catascopium  •  Northern  United  States  to  the  Rocky 
Mountains,  Canada  and  northward;  var.  sumassi:  Idaho,  Washing- 
ton and  British  Columbia. 

Ottawa,  Canada  !  Ungava,  Labrador  !  Lake  Winnipeg,  Manitoba  ! 
Hudson  Bay  drainage  of  Keewatin  !  Moose  River  at  Moose  Factory, 


78  LAND    AND    FRESH    WATER    MOLLUSKS 

Hudson  Bay  !  Fort  Resolution,  Great  Slave  Lake  !  Winisk,  Kawino- 
gans,  and  Attawapiskat  Rivers,  S.  E.  Keewatin  !  (Mclnnes). 


Fig.  59.    Lymncea  catascopium  Say,  var.         Fig.  60.    Lymncea  catascopium  Say 
5«»»aj«Bd.  (British  Columbia).  (Delaware). 

Var.  sumassi:  Snake  River,  Idaho!  Lake  Washington,  Seattle! 
Sumas  Prairie,  British  Columbia. 

Quite  variable  and  frequently  confounded  with  L.  adelince^  L.  buli- 
moides^  L.  solida^  etc.  The  Pacific  Coast  form  is  quite  close  to  the 
typical  form  of  the  species,  but  is  thinner,  less  uniform,  and  some- 
times larger.  Binney's  figure  57  is  made  from  a  specimen  probably 
of  a  rather  sw^ollen  variety  of  palustris. 


♦Lymnaea  (Stagnicola)  adelinae  Try  on. 

Limnaa  adelincE  Tryon,   Mon.  Limn.,   p.   82  (108),  pi.  xvill,   fig.  6,   1872 
(San  Francisco,  Calif.). 

Range.  —  California  to  Vancouver  Island,  B.  C. 

A  small  species,  recalling  Z.  bulimoides  rather  than  catascopium., 
and  perhaps  identical  w^ith  Lea's  original  bulimoides^ 
as  indicated  by  his  types,  but  not  with  L.  techella 
Haldeman,  which  is  very  generally  labelled  buli- 
moides. 

Fig.  61.  Lym-    Lymnaea  (Stagnicola?)   perpolita   n.  sp.     Plate  11, 

neea  adelincB.  r-         £    o 

figs.  6,  5. 

Shell  small,  translucent,  dark  amber  color,  with  a  darker  line  at 
resting  stages  ;  smooth,  except  for  fine  lines  of  growth,  brilliantly 
polished ;  whorls  four,  tumid,  rapidly  increasing,  separated  by  a  pro- 
nounced suture ;  spire  short,  rather  obtuse ;  aperture  ovate,  longer 
than  the  spire,  with  a  very  thin  wash  of  callus  on  the  spire,  the  pillar 
lip  slightly  reflected,  with  a  small  perforate  umbilicus  behind  it ;  pillar 
straight,  with  no  twist  or  fold,  outer  lip  thin,  sharp.  Length  of 
shell  1 1  ;  of  aperture  7  ;  breadth  of  shell  8.5  ;  of  aperture  4.5  mm. 

Range.  —  Nushagak,  Bristol  Bay,  Alaska. 

This  shell  is  so  elegantly  polished  that  it  may  be  an  Amphipeplea. 
It  has  the  rich  dark  amber  color  of  some  Succineas.     I  have  seen  but 


% 


FAMILY    LYMN^ID^  79 

one  specimen,  but  some  young  shells  from  Sonoma  Co.,  Calif.,  col- 
lected by  Hemphill,  may  belong  to  it.  The  latter  are  proportionally 
stouter  and  are  of  a  pale  straw  color.  The  polish  of  the  surface  and 
the  straight  pillar  are  alike  in  both,  yet  I  hesitate  to  unite  them.  No 
other  American  species  has  an  equally  polished  surface  so  far  as  I 
have  observed. 

Lymnaea  (Stagnicola)  bulimoides  Lea. 

LimncEa  bulimoides  Lea,  Proc.  Am.  Phil.  See,  ii,  p.  33,  1841  ;  Trans.  Am. 
Phil.  Soc,  IX,  p.  9,  1844.  —  Haldeman,  Mon.  Limn.,  p.  44,  pi.  xiii, 
figs.  9,  10,  1842.  — BiNNEY,  op.  cit.,  p.  61,  fig.  96,  1865  (Oregon). 

Range. — Oregon,  California,  Texas,  Nevs^  Mexico, 
Dakota,  the  United  States  west  of  the  Mississippi 
(and  northward.?) 

Oregon  !  (Nuttall)  Columbia  River  near  Fort  Van- 
couver, Wash. !  Moose  Rivei  at  Moose  Factory,  Hud-  ^°*   ^*.    ^"^ 

'"^<*    ouhmotdes 
son  Bay  (Drexler)  ?  Lea.  (Typical. ) 

This  species  has  been  generally  confounded  with  L. 
techella  Haldeman,  which  seems  to  be  distinct,  having  a  more  stumpy 
form  and  larger  umbilicus,  recalling,  as  Binney  observes,  his  Buli- 
tnulus  pilula.  According  to  Lea's  types,  very  few  of  the  localities 
cited  for  this  species,  away  from  the  Pacific  Coast,  are  reliable.  I  sus- 
pect the  shell  from  Hudson  Bay,  collected  by  Drexler,  is  a  young  cata- 
scopium  or  caper ata  and  not  the  true  bulimoides. 

Lymnsea  (Stagnicola)  caperata  Say. 

Lymneus  caperattis  Say,  New  Harmony  Disseminator,  11,  p.  230,  1829. 
Hntnea  caperata  Haldeman,  Mon.  Limn.,  p.  34,  pi.  xi,  figs.  1-9,  1842. 
JJmncea  umbilicata  Anxus,  Am.  Journ.  Sci.,  xxxix,  p.   374,    1840;  Boston 

Joum.  N.  Hist.,  in,  p.  325,  pi.  iii,  fig.  14,  1840. — Gould,  Inv.  Mass., 

p.  218,  fig.  149,  1841. 

Range.  —  Northern    United    States,  west   to    the 
Rocky  Mountains  and  northward. 

Manitoba  ;  at  Pine  Creek,  Pembina,  and  Lake  Win- 
nipeg.    Alberta ;    at  Red  Deer  and  McLeod.     The 
lower  Saskatchewan  near  Lake  Winnipeg.     Hudson 
Fig.  63.  Lym-     ^^7  drainage  at  Moose  Factory.     I  feel  strong  doubts 
ntea  caperata.        as  to  the  validity  of  this  species,  which  may  prove 
entirely  heterogeneous. 

Lymnsea  (Stagnicola)  anticostiana  n.  sp.    Plate  ii,  figs.  4,  5. 

Shell  acute,  slender,  with  a  blunt  reddish  nucleus  and  seven  well- 
rounded  whorls ;  suture  deep,  the  whorls  slowly  enlarging ;  the  last 


8o  LAND    AND    FRESH    WATER    MOLLUSKS 

whorl  subcompressed  laterally ;  aperture  elongate-ovate,  about  2f  times 
its  length  being  equal  to  the  length  of  the  shell ;  margin  thickened,  and 
continuous  over  the  body,  reflected  over  an  umbilical  chink  behind  the 
pillar  but  not  quite  closing  it ;  pillar  with  a  marked  fold ;  surface  with 
close-set  fine  axial  elevated  lines  in  harmony  with  the  lines  of  growth, 
and  crossed  by  microscopic  revolving  striae  which  sagrinate  the  surface  ; 
there  are  also  malleations,  obscure  sparse  revolving  ridges,  etc.,  on  in- 
dividual specimens.  Length  of  shell  19;  aperture  7.0;  max.  diam. 
7.0,  of  aperture  4.5  mm. 

Range.  —  Pleistocene  marl  of  Marl  Lake,  Anticosti  Island  (Sir 
William  Logan  and  Dr.  J.  Schmitt).     Recent? 

This  interesting  species  resembles  somewhat  L.  desidiosa^  to  which 
it  has  usually  been  referred,  but  it  has  two  more  whorls  and  a  more 
slender  and  elevated  spire,  and  in  most  specimens  a  more  parallel -sided 
aperture.  I  am  unable  to  say  whether  it  occurs  in  the  recent  state,  but 
the  numerous  specimens  I  have  seen  are  all  fossils.  Dr.  Lea  had 
labelled  his  specimens  'Z..  acuta  Lea,'  doubtless  forgetting  his  own 
species  of  the  same  name,  which  is  a  very  different  shell. 

Uncertain  Species. 
There  are  several  nude  names  in  the  literature  which  cannot  be  iden- 
tified and  yet  may  puzzle  the  student  who  is  unaware  that  they  have 
not  been  described.  Of  such  are  L.fossaria  J.  de  C.  Sowerby  (1836) , 
in  Richardson's  Fauna  Boreali  Americana ;  L.  petitii'Be^ck  (1838), 
listed  from  Newfoundland  in  his  '  Index ' ;  and  X.  opacina  Bell  (1858) , 
listed  in  the  Annual  Report  of  the  Canadian  Geological  Survey. 

Genus  Planorbis  Muller. 

Planorbis  Petiver,  Gazophyl.  Nat.  et  Artis  Dec,  p.  16,  tab.  10,  fig.  11,  1702 
(not  binomial).  The  species  figured  is  Helix  planorbis  Linne,  Fauna 
Suecica,  p.  527,  1761. — Guettard,  Mem.  Acad.  Roy.  des.  Sci.  (1756), 
p.  151,  1 762  (not  binomial),  first  sp.  Plan,  brun.,  after  Lister,  Anim.  Angl., 
p.  143,  pi.  II,  fig.  26  (=  Helix  comeus  Linne). —  Geoffroy,  Traite  Som. 
des  Coq.  Fluv.  Paris,  pp.  81,  84,  1767  (not  binomial),  §  i,  Helix  cornea 
Linne  ;  Ibid.,  translation  by  Martini,  Niirnberg,  pp.  10,  75,  1767. 

G7r^/'«^  Adanson,  Hist.  Senegal,  p.  7,  1757  (not  binomial),  sp.  figured  re- 
sembles P.  parvus  Say. 

<  Planorbis  Muller,  Verm.  Terr.,  11,  p.  152,  1774,  no  type  selected  ;  Prodr. 
Zool.  Dan.,  pp.  xxx,  238,  1775. —  Brugui^re,  Enc.  Meth.,  i,  p.  xvi, 
1789,  nude  name. —  Bolten,  Mus.  Bolt.,  p.  51,  1798. —  Lamarck,  Pro- 
drome, p.  76,  1799  ;  Syst.  des  An.  s.  Vert.,  p.  93,  1801. — Draparnaud, 
Tabl.  Coq.  Terr,  et  Fluv.,  pp.  30,  42,  1 801.— Schumacher,  Essai,  p. 
255,  1817;  not  of  Perry,  181 1. 

=Planorbis  Montfort,  Conch.  Syst.,  ll,  p.  270,  1810,  selects  as  type  P. 
comeus  L. 


FAMILY    LYMN^ID^  8l 

Orbis  ScHROTER,  Journ.  Steinr.  u.  Konch.,  iii,  p.  lo,  1776,  an  error  of  cita- 
tion for  Planorbis  Argenville. 

f^/<r^  Anonymous  in  Mus.  Calonn.,  p.  58,  1797,  Helix  cornea  Linn6.  Not 
Vortex  Oken,  181 5. 

<  Anisus  Studer,  Syst.  Verz.,  p.  23,  1820  (= Planorbis -\-  Physa). 

^  Anisus  FiTZiNGER,  Verz.,  p.  m,  1833;  not  of  Dujardin,  1821. 

f  Corfiu  Schumacher,  Essai,  p.  255,  1817,  not  of  Born,  1778. 

^  Spiralina  Hartmann,  Syst.  Uebers.,  tab.  1840.  (Nude  name.)  No  type 
cited. 

Planorbarius  Dumeril,  Zool.  Anal.,  p.  164,  1806. 

Coretus  Gray  (not  Adanson),  P.  Z.  S.,  1847,  p.  180,  P.  corneus  L. — Mrs. 
Gray,  Figs.  Moll.  An.,  iv,  p.  119,  1850. —  Moquin  Tandon,  Moll.  Terr, 
et  Fluv.,  II,  p.  423,  1855. — Gray's  Turton's  Man.,  ed.  11,  p.  233, 
1857. 

Spirodiscus  Stein,  Schn.  u.  Muschein  Berlins,  p.  73,  1850. — Morch,  Vidensk. 
Meddels.  Kjobn.,  1864,  p.  309. — Westerlund,  Acta  Soc.  Fauna  Fen- 
nica,  XIII,  No.  7,  p.  112,  1897  ;  Acta  Acad.  Sci.  Slav.  Merid.,  Zagrabiae, 
CLI,  p.  120,  1902  ;  S.  corneus  (Linne). 

Tropidiscus  Westerlund,  Fauna  Pal.  Reg.,v,  p.  65,  1885,  not  of  Stein; 
Acta.  Acad.  Sci.  Slav.  Merid.,  Zagrabiae,  CLi,  p.  120,  1902;  Helix  plan- 
orbis Linn6. 

t  Caillaudia  Bourguignat,  Hist.  Mai.  de  I'Abyssinie,  p.  128,  1883;  ist  sp. 
C.  angulata  Bourg.,  pi.  viii,  figs.  49-52,  op.  cit, — Westerlund,  Acta 
Acad.  Sci.  Slav.  Merid.,  Zagrabiae,  cli,  p.  139,  1902  (a  deformed  or 
monstrous  form  of  Planorbis). 

Subgenus  Planorbis  s.s. 

T3^e  Planorbis  corneus  Miiller. 

(Synonymy  of  the  group  given  under  the  generic  name.) 

Section  Planorbina  Haldeman. 

Planorbina  Haldeman,  Mon.  Limn.,  Physada,  p.  14,  1842,  no  type  cited. 
Menetus   Fischer,    Man.,    p.  509,    1883;    P.  guadeloupensis  Sowerby  ;   not 

Menetus  Adams,  1855. 
Anisus  Gray,  P.  Z.  S.,  1847,  p.  181  ;  P.  olivaceus  Spix  ;  not  Anisus  Studer, 

1820. 

Subgenus  Helisoma  Swainson. 

Helisoma  Swainson,  Malac,  p.  337,  1840  ;  P.  bicarinatus  Sowerby. 
Taphius  H.  and  A.  Adams,  Gen.  Rec.  Moll.,  11,  p.  262,  1855  ;  P.  andecolus 

Orbigny. 
?  Anisopsis  Sandberger,  Land  u.  Siissw,  Conch,  d.  Vorwelt,  p.  958,  1875  ;  P. 

loryi  Co({.,  and  P.  calculus  Sandb.,  Jurassic. 

Section  Pierosoma  Dall,  nov. 
Helisoma  (sp.)  Auct.,  not  of  Swainson  ;  P.  trivolvis  Say. 

Section  Planorbella  Haldeman. 

Planorbella  Haldeman,  Mon.  Limn.,  Physadce,  p.  14,  1842  ;  P.  campanula's 
Say. 


82  LAND    AND    FRESH    WATER    MOLLUSKS 

Adula  H.  Adams,  P.  Z.  S.,    i86i,  p.    145  ;  P.  muUivolvis  Case,   not  Adula 

H.  and  A.  Adams,  1857. 
Anccrus  H.  Adams,  P.  Z.  S.,  1869,  p.  275  ;  not  Ancaus  Fauvel,  1863. 

Subgenus  Tropidiscus  Stein. 

Tropidiscus  Stein,  Schn.  u.  Muscheln  Berlins,  p.  76,  1850 ;  P.  complanatus 

Stein  (  =  marginatus  Drap.  +  umbilicatus  Miiller). 
Trophidiscus  H.   and  A.   Adams,   Gen.    Rec.    Moll,,    n,   p,    263,    1855,   in 

synonymy. 
Anisus  FiTZiNGER,  Verz,  p.   in,   1833,  ex  parte,  not  of  Studer,    1820,  nor 

Dujardin,  1821. 
Gyrorbis  Moquin  Tandon,  Hist.  Moll.  Terr,  et  Fluv.  de  France,  pp.  423,  428, 

1885  (not  of  Fitzinger,    1833);    P.    carinatus  Miiller;  Gray's    Turton, 

new  ed.,  p.  237,  1857. 
Tropodiscus  Surbeck,  Moll.  Faun.  Vierwaldstattensis,  Rev.  Suisse  de  Zool., 

VI.  p.  435,  1899. 
'^Tropidiscus  Westerlund,  Act.  Soc.  Fauna  Fennica,  xiii,  p.  113,  1897,  ist 

sp.  P.  umbilicatus  Miiller. 
';^  Dip/odisctis  WESTEKhutiD,  op.  cit.,  p.  115,  1897,  I  St  sp,  P.  vortex  Linn£. 

Section  Paraspira  Dall,  nov. 

Spirorbis   Swainson,    Malac,    p.   337,    1840;    P.  rotundatus  Poiret  ( + /*. 

vulgaris  Swains.),  not  Spirorbis  Daudin,    Vermes,  1800. 
Gyrorbis  Morch,    Vidensk.   Meddel.   Kjob.,   for  1863,   p.  313,    1864,  not  of 

Fitzinger,  1833. 
Planorbis  (sp.)  Agassiz,  in  Charpentier,  Fauna  Helv.,  p.  21,  1837. 
Anisus  (sp.)  Fitzinger,  Verz,  p.  iii,  1833  ;  not  of  Studer,  1820. 

Subgenus  Hippeutis  Agassiz. 

Hippeutis  Agassiz,  in  Charpentier,  Fauna  Helv.,  p.  22,  1837  ;  P.  complanatus 
Drap.  (  =  /*.  fontanus  Lightfoot).  —  Hartmann,  Syst.  Uebers,,  table, 
1840  ;  Erd.  u.  Sussw.  Gast.,  pp.  51,  87,  1844.  — Gray,  in  Turton' s  Man., 
ed.  II,  p.  243,  1857. —  Morch,  Vidensk.  Meddel.,  1863,  p.  316,  1864. 

Hippeutes  Mrs.  Gray,  Figs.  Moll.  An.,  iv.,  p.  119,  1859. 

Section  Menetus  H.  and  A.  Adams. 

Menetus  H.  and  A.  Adams,  Gen.  Rec.  Moll.,  11,  p.  262,  1855  ;  no  type 
selected  (not  of  Chenu,  1869,  or  Fischer,  1883).  —  Binney,  Land  and 
Fw.  Sh.  N.  Am.,  11,  p.  125,  1865. 

Menetus  Dall,  Ann.  Lye.  N.  Hist.  N.  Y.,  ix,  p.  351,  1870;  P.  opercularis 
Gould.  —  Clessin,  Conch.  Cab.,  ed.  11,  xvii,  p.  33,  1886. — Wester- 
lund, Act.  Acad.  Sci.  Slav.  Merid.,  Zagrabiae,  CLi,  p.  120,  1902,  P. 
boissyi  Pot.  et  Mich. 

Heterodiscus  Westerlund,  op.  cit.,  1902,  not  of  Sharp,  1886,  Insecta.  P. 
libanicus  Westerlund, 

Section  Drepanotrema  Crosse  and  Fischer. 

Drepanotrema  C.  and  F.,  Miss.  Sci.  Mexique,  11,  pp.  59,  75,  pi.  xxxiii,  fig. 
2,  1880;  P.  yzabalensis  C.  &  F, ;  Fischer,  Man.,  p.  509,  1883. 


FAMILY    LYMN^EID^  83 

Section  Bathyomphalus  Agassiz. 

Baihyomphalus  Agkssiz,  in  Charpentier,  Fauna  Helv.,  p.  20,  1837  ;  P.  contortus 
Drap. — Hartmann,  Syst.  Uebers.  Gast,  table,  1840.  —  Westerlund 
Acta  Acad.  Sci.  Slav.  Merid.,  Zagrabiae,  cli,  p.  120,  1902. 

Polygyrus  Gray,  P.  Z.  S.,  1847,  p.  181  ;  P.  contortus  Muller  ;  not  of  Beck, 
1837,  nor  Polygyra  Say,  1818. 

Bathyomphalus  Gray,  in  Turton,  Man.,  2d  ed.,  p.  244,  1857. 

Discoidina  Stein,  Schn.  u.  Muscheln  Berlins,  p.  82,  1850  ;  P.  contortus 
Muller. 

Subgenus  Gyxaulus  Agassiz. 

Gyraulus  Agassiz,  in  Charpentier,  Fauna  Helvetica,  p.    21,  1837  ;   ist  sp.  P. 

hispidus  Drap.  {=  albus  MiiUer). — Hartmann,    Syst.    Uebers.,  table, 

1840;  Gast.,  V,  pp.  89,   95,  1844. —  MoQUiN  Tandon,  Hist.  Moll.  Terr, 

et  Fluv.,  II,  p.  438,  1855. 
Planaria  Brown,   111.   Conch.  Gt.   Brit.,  expl.  pi.   51,   figs.  48,  49^^,  1827  ; 

not  Planaria  Muller,  1776. 
Trochlea  Haldeman,  Am.  Joum.  Sci.,  xlii,  p.  216,  1841. 
Giraulus  MoQUiN  Tandon,  Hist.  Moll.  Terr,  et  Fluv.  de  France,  11,  p.  423, 

1855. 
Nautilina  (pars)  Stein,  Schn.  u.  Muscheln  Berlins,  p.  80,  1850. 
Gyrulus  Gray,  in  Turton,  Man.,  2d  ed.,  p.  234,  1857,  in  syn. 
Gyraulus  Gray,  op.  cit.,  p.  234,    1857,  P.  albus  Muller. —  Westerlund, 

Acta  Acad.  Sd.  Slav,  Merid.,  Zagrabiae,  cli,  p.  121,  1902. 

Section  Armiger  Hartmann. 

.<4/7«/^<?r  Hartmann,  Syst.  Uebers.,  table,  1840;  Gast.,  v,  p.  172,  1842  ;  P. 

crista  (L.). — Westerlund,  Acta  Acad.  Sci.  Slav.  Merid.,  cli,  p.  I2i, 

1902. 
Nautilina  (sp.)  Stein,  Schn.  u.  Muscheln  Berlins,  p.  81,  1850. 

Section  Torquis  Dall,  nov. 

Type  P.  parvus  Say. 

{Incerte  sedisJ) 

?  Section  Heterodiscus  Westerlund. 

Heterodiscus  Westerlund,  Rad.  Jugoslav.  Akad.  (Acta  Acad.  Sci.  Slav. 
Merid.),  en,  p.  120,  Zool.  Rec,  XL,  1903,  Moll.,  p,  63.  Type  Planorbis 
libanicus  Westerlund,     Not  Heterodiscus  Sharp,  Insecta,  1 886, 

.?  =  Planorbina  Haldeman,  1842,  q.  v. 

The  genus  Planorbis  is  frequently  ascribed  to  Guettard  or  Geoff roy, 
neither  of  whom  accepted  (in  the  papers  where  this  name  appears)  the 
Linnean  nomenclature.  If  we  are  to  cite  non-Linnean  authors  we 
must  go  back  much  further,  for  Petiver  used  the  name  in  1 702  for  a 
species  which  Linn6  afterward  named  Helix  spirorbis.  Another 
non-Linnean  name  is  Coretus  of  Adanson,  which  he  applied  to  a 
minute  species  an  eighth  of  an  inch  in  greatest  diameter.  Gray  in 
1847,  ^y  some  error  cites  Planorbis  corneus  as  Adanson's  type,  which 


84  LAND    AND    FRESH    WATER    MOLLUSKS 

is,  of  course,  absurd.  The  first  author  to  introduce  Planorbis  to 
binomial  literature  was  O.  F.  Miiller,  but  as  he  used  it,  it  was  applicable 
to  all  aquatic  Pulmonates  with  filiform  tentacles,  thus  including  Physa. 
Cuvier  in  1798  cited  three  species,  of  which  P.  corneus  was  the  first 
and  P.  cornu-arietis  the  second.  In  1799  Lamarck  cited  the  second 
species,  and  repeated  this  citation  in  1801.  But  P.  cornu-arietis^  of 
which  the  soft  parts  and  operculum  were  then  unknown,  does  not 
agree  with  Lamarck's  diagnosis  and  cannot  be  accepted  as  a  type  of 
the  genus  Planorbis.  Draparnaud  names  no  types,  and  only  in  18 10 
does  Montfort  establish  definitely  the  type  of  the  genus  as  P.  corneus. 
Subsequent  selection  of  other  types  by  later  authors  is,  of  course,  of 
no  effect.  Anisus  Studer  was  an  exact  synonym  of  Planorbis  Miil- 
ler, not  Montfort,  but  Fitzinger,  in  1833,  made  an  effort  to  retain  the 
name  for  a  section  of  the  true  Planorbes.  It  is  probable,  however,  that 
the  name,  which  was  intended  to  comprise  two  older  genera  already 
named,  should  be  entirely  eliminated  from  accepted  nomenclature,  as 
a  gross  violation  of  the  rules.  At  any  rate  the  name  was  used  for 
a  beetle  by  Dujardin  in  182 1,  and  no  subsequent  use  of  it  is  advisable 
for  Mollusks. 

Little  is  known  of  the  anatomical  characteristics  of  the  various 
species,  but  much  similarity  is  noted  among  those  for  which  data  are 
available.  As  to  the  shells,  a  wide  variation  is  observable  in  form  and 
sculpture,  though  as  usual  the  peripheral  species  grade  toward  each 
other  in  the  several  groups.  The  great  majority  of  the  species  present 
the  peculiarity  of  the  whorls  rising  above  the  original  apex,  which 
becomes  basal,  the  shell  (apparently  sinistral)  thus  becoming  what  has 
been  called  ultra-dextral.  The  most  obvious  characters  of  the  latter 
may  be  contrasted  as  follows  : 

Subgenus  Planorbis  s.  s.     Shell  discoid,  ultra-dextral,  large,  with  a 
moderate  number  of  gradually  enlarging  whorls  rounded  above  and 
below ;  the  aperture  slightly  and  gradually  expanded,  with  its  margin 
simple  and  sharp.     Type  P.  corneus  Miiller. 
Section  Planorbina  Haldemann.     Shell  like  Planorbis  s.  s.  but  verti- 
cally compressed,  with  smaller  and  more  numerous  whorls  and  a 
very  oblique  aperture.     Type  P.  olivaceus  Spix. 
Subgenus  Helisoma  Swainson.     Shell  of  moderate  size,  few  whorled, 
the  whorls  carinate  above  and  below  and  rapidly  enlarging ;  spire 
and  base  funicular,  aperture  suddenly  expanded,  with  a  thickened 
peritreme.     Type  P.  bicarinatus  (Say)  Sowerby. 
There  is  no  doubt  that  Sowerby's  and  Say's  species  are  identical.     I 
am  unable  to  find  distinctive  characters  in  figures  or  diagnoses  which 


FAMILY    LYMN^ID^E  85 

would  differentiate  Taphius  Adams  from  Hells oma ;  and  Anlsopsls 
Sandberger,  from  the  Jura,  is  very  similar,  though  the  aperture  is  not 
preserved  in  the  fossils  and  may  have  been  simple. 
Section  Plerosoma  Dall       Shell  large,  high,  with  few  transversely 
sculptured  whorls ;  the  early  whorls  carinate  and  flattened  above, 
funicular  below ;  in  the  adult  the  flattened  apex  is  usually  depressed 
below  the  upper  level  of  the  ultimate  whorl ;  the  aperture  is  suddenly 
expanded   and  thickened.     Type  P.  trivolvls  Say. 
Section  Planorbella  Haldeman.  Like  Hellsoma  but  smaller,  with  more 
numerous  whorls,  with  the  last  whorl  strongly  constricted  behind  a 
campanulate  aperture ;  a  fiattish  or  even  slightly  convex  upper  sur- 
face ;  the  base  funicular.     Type  P.  campanulatus  Say. 
The  P.  multlvolvls  Case  differs  from  the  type  of  Planorbella  chiefly 
by  its  more  numerous  and  closely  coiled  early  whorls.     In  both  a 
second  year's  growth  shows  a  varix  due  to  the  retention  of  the  aper- 
ture of  the  preceding  year.     Two  preoccupied  names  were  applied  to 
P.  multivolvis  by  Adams,  but  a  study  of  specimens  leads  to  the  con- 
clusion that  its  separation  is  unwarranted. 

Subgenus  Tropidiscus  Stein.  Shell  depressed,  the  adult  periphery 
angular  or  carinate,  the  aperture  oblique,  slightly  expanded,  simple. 
Type  P.  umbilicatus  MuUer  {^■\-  P.  complanatus  Stein) . 
Section  Tropidiscus  s.  s.  Shell  moderately  large  and  with  compara- 
tively few  rapidly  increasing  whorls  of  which  the  junior  portions 
are  not  keeled.     Type  P.  umbilicatus  Miiller. 

This  subgenus  was  called  '  Gyrorbis  Agassiz,'  by  Moquin  Tan- 
don,  but  Agassiz  never  proposed  any  such  genus  or  group,  the  name 
Gyrorbis  having  been  applied  to  a  subdivision  of  Valvata  by  Fitz- 
inger.  Moquin  Tandon's  error  was  copied  by  Gray,  and  later  by 
Westerlund,  who,  still  later,  having  become  aware  that  Fitzinger's 
name  existed,  proposed  for  the  group  already  named  by  Stein,  the 
name  Diplodiscus ;  which  naturally  becomes  a  synonym  of  Tropi- 
discus Stein.  Nevertheless,  since  Westerlund  arranged  his  really 
typical  '  Gyrorbis '  under  Tropidiscus.^  and  grouped  under  his  new 
name  the  species  of  which  P.  vortex  is  an  example  (though  without 
mentioning  any  type)  and  gave  a  suitable  diagnosis,  it  may  not  be 
stretching  the  rules  of  nomenclature  too  far  to  retain  his  name  for  the 
following  section. 

Section  Diplodiscus  Westerlund  (restricted).  Shell  small,  with 
numerous  slowly  enlarging  whorls  keeled  or  angulate  from  the 
beginning.     Type  P.  vortex  Linn^. 


86  LAND    AND    FRESH    WATER    MOLLUSKS 

Section  Paraspira  Dall,  nov.  Shell  resembling  Diplodiscus^  but 
with  the  whorls  rounded  throughout,  and  the  aperture  simple, 
hardly  expanded.     Type  P.  rotundatus  Poiret. 

Subgenus  Hzppeutis  Agassiz.  Shell  small,  lenticular,  with  a  small 
number  of  rapidly  increasing  whorls,  the  last  enveloping  a  large 
part  of  the  preceding  whorl ;  apex  slightly  depressed,  base  with  a 
narrow  umbilicus,  aperture  oblique,  with  a  thin  sharp  margin.  Type 
P.fontanus  Lightfoot,  European. 

Section  Drepanotrema  Crosse  and  Fischer.  Shell  resembling  Hip- 
peutis^  but  less  depressed,  the  whorls  with  a  rounded  periphery 
widest  at  the  base,  giving  a  domelike  profile,  umbilicus  variable, 
from  narrow  to  very  wide.  Type  P.  yzabalensis  C.  and  F. 
This  group  occurs  in  the  Antilles,  Mexico,  Central  and  South 
America,  where  it  represents  the  Palearctic  Hippeutis. 

Section  Menetus  H.  and  A.  Adams.  Like  Hippeutis^  but  the  last 
whorl  not  enveloping  the  preceding  whorls  to  any  marked  extent. 
Type  Planorbis  opercularis  Gould. 

Section  Bathyomphalus  Agassiz.  Shell  like  Drepanotrema^  but  with 
numerous  closely  coiled  whorls,  a  flattish  summit  with  the  periphery 
nearer  to  it  than  to  the  base,  the  umbilicus  moderate,  exposing  less 
of  the  coil  than  the  summit  shows.     Type  P.  contortus  Drap. 

Subgenus  Gyraulus  Agassiz.  Shell  small,  flattish,  with  few,  rapidly 
increasing  whorls,  fully  exposed  above  and  below,  with  a  nearly 
median  periphery,  spirally  striate  and  hispid ;  aperture  simple, 
sharp-edged,  oblique.     Type  Planorbis  albus  Miiller. 

Section  Torquis  Dall,  nov.  sect.  Like  Gyraulus  s.  s.  but  with  more 
rounded,  less  rapidly  increasing  whorls,  not  hispid  or  spirally  striate, 
the  aperture  expanded  and  slightly  thickened  in  the  adult.  Type 
P.  parvus  Say. 

Section  Armiger  Hartmann.     Shell  small,  with  few,  rapidly  increas- 
ing, costate  whorls,  the  costae  projecting  at  the  periphery ;  the  form 
in  a  general  way  like  Gyraulus. 
A  discussion  of  the  species  follows. 

*  Planorbis  (Planorbina)  glabratus  Say. 

Planorbis  glabratus   Say,    Journ.   Acad.    Nat.   Sci.,    I,   p.   280,    1818  (South 

Carolina). 
Planorbis  lentus  Say,  Am.  Conch.,  vi,  pi.  iv,  fig.  i,  1834  (New  Orleans). 

This  species  is  by  no  means  always  polished,  and  on  a  dull  speci- 
men of  it  I  believe  the  later  P.  lentus  Say  to  have  been  founded, 
though  the  latter  name  has  been  widely  misapplied  to  senile  specimens 


FAMILY    LYMN^ID^ 


87 


l-.^.L-,.  Plan- 
orbis  bicarina- 
tus  Say. 


of  trivolvis  such  as  occur  in  the  north  and  east,  if  not  throughout  the 

range  of  the  latter. 

Planorbis  (Helisoma)  bicarinatus  Say. 

Planorbis  bicarinatus  Say,  Nicholson's  EncycL,  ist  ed.,  vol.  11  (no  pagina- 
tion), No.  2,  pi.  I,  fig.  4,  1817  (Lake  Erie)  ;  not  of  Lamarck,  1822. — 
BiNNEY,  Land  and  Fw.  Sh.  N.  Am.,  11,  p.  123,  fig.  205,  1865. 

Helix  engonata  Rackett,  1822  ;  +  Planorbis  engonatus  Conrad,  1834. 

Range.  —  The  United  States  east  of  the  Rocky  Mountains ;  east- 
ern Canada. 

Lake  Superior  to  Lake  Winnipeg  !    Lake  Manitoba  ;   Moose  Fac- 
tory, Hudson  Bay  !  the  lower  Saskatchewan  River  at  Grand  Rapids  ! 
Knee   Lake,   Keewatin !    Portland,    Oregon !    Yaqui 
River,  W.  Mexico  ! 

This  well  defined  species  has  probably  been  carried 
down  stream  from  the  sources  of  the  Columbia  River, 
in  the  same  manner  as  some  other  east  American  spe- 
cies. It  cannot  be  regarded  as  permanently  estab- 
lished on  the  Pacific  slope,  as  yet.  It  varies  consider- 
ably in  size,  and  for  exceptionally  developed  specimens 
from  Benzie  Co.,  Mich.,  Walker  has  proposed  the 
varietal  name  major. 

Planorbis  (Pierosoma)  corpulentus  Say. 

Planorbis  corpulentus  Say,  Long's  Exp.,  11,  p.  262,  pi.  xv,  fig.  9,  1824  (not 

of  Binney  et  ai.)  —  Bryant  Walker,  Nautilus,   xiii,   No.   12,  April, 

1900,  pp.  133-138. 

Range. — Northern  Ontario  from  Lake  Simcoe  to 
Rainy  Lake,  Lake  of  the  Woods,  Winnipeg  River 
and  Lake !  to  Vermilion  Lake,  Lat.  56°  30',  in 
Athabaska. 

Knee  Lake,  Keewatin  !  Isle  h.  Lacrosse  Lake  !  and 
English  River  !  Rat  Portage  ;  northern  Michigan  and 
Minnesota. 

This  well  marked  species  was  unknown  to  Binney, 
and  has  been  united  mistakenly  with  trivolvis  and 
others.  It  belongs  to  the  colder  northeastern  portion 
of  the  continent  and  its  complete  range  is  yet  un- 
known. It  has  not  been  identified  from  the  region  west  of  the  Rockies. 
Mr.  Walker's  note  on  this  species  may  be  consulted  with  profit. 

Planorbis  (Pierosoma)  binneyi  Tryon. 

Planorbis  binneyi  Tkyo's,  Am.   Joum.  Conch.,   iii,  p.    197,    1867. —  Halde- 

MAN,  Mon.   Limn.,  19,  pi.  iii,  figs.  7-9,  1844.- 

Sh.  N.  Am.,  II,  p.  103,  fig.  175,  1865. 


Fig.  65.  Plan- 
orbis corpulen- 
tus Say.     \. 


-Binney,  Land  and  Fw, 


08  LAND    AND    FRESH    WATER    MOLLUSKS 

Range. —  West  of  the  Rockies  and  east  of  the  Cascade  Mountains 
on  the  Pacific  slope. 

Oregon  (Nuttall)  ;  Lewis  or  Snake  River,  Oregon !  Clear  Lake, 
Calif. !  In  British  Columbia  in  eastern  Kootenai  Lake,  Lake  Siniak- 
wateen,  and  Osoyoos  Lake  ! 

As  pointed  out  by  Binney,  this  is  quite  distinguishable  from  any 
form  of  trivolvis ;  it  differs  from  the  true  corpulentus^  with  which  it 
was  long  confounded,  in  its  sparser  and  less  regular  axial  sculpture, 
larger  and  less  campanulate  aperture,  and  in  the  greater  distance  of  the 
carina  from  the  axis.  Its  whorls  increase  more  rapidly  than  in  P. 
traskii  Lea,  or  even  P.  ammon  Gould,^  and  its  sculpture  is  markedly 
coarser  and  less  regular  than  in  either  of  the  two  last  cited.  It  is  not 
known  north  of  British  Columbia  or  east  of  the  Rocky  Mountains. 


Figs.  66,  67.     Planorbis  binneyi,  showing  animal  and  shell. 

Planorbis  (Pierosoma)  trivolvis  Say. 

Planorbis  trivolvis  Say,  Nicholson's  Encyc,  isted.,  11  (no  pagination),  pi.  il, 

fig.  2,  1817  ;    Am.  Conch.,  vi,  pi.  54,  fig.  2,  1834  (French  Creek,  Lake 

Erie). 
Planorbis  macrostotnus  Whiteaves,  1863  (abnormal)  ;  -f  P.  lentus  Gould,  and 

many  other  writers,  but  not  of  Say  ;  +   P.   lumens  various  California 

writers. 
Planorbis  subcrenatus  Carpenter,  P.  Z.  S.,  1856,  p.  220. 

Range.  —  The  typical  form  belongs  to  the  entire  Atlantic  drainage 
of  North  America  and  the  Mississippi  Valley  and  northward  to  the 
Etchimamish  River. 

English  River,  Keewatin ;  Lake  Winnipeg,  Manitoba ;  Cypress 
Hills !  Assiniboia ;  Prairie  Lake,  Red  River  of  the  North ! ;  the 
Saskatchewan  River,  Laggan,  Egg  Lake,  Red  Deer,  McLeod,  and 
Olds,  Alberta;  Lake  Isle  Lacrosse,  Athabaska;  Great  Slave  Lake, 
at   Fort   Resolution !    and  the   Mackenzie  River   at  old   Fort  Simp- 

1  These  two  species,  judged  by  their  types,  which  are  before  me,  are  suffi- 
ciently distinct  from  any  of  those  which  have  been  confounded  with  them.  In- 
deed the  true  P.  traskii  from  Kern  Lake,  Calif.,  is  one  of  the  most  remarkable 
species  in  our  fauna.  It  was  also  found  by  me  at  Stockton,  Calif.,  and  seems  to 
have  been  unknown,  autoptically,  to  Binney. 


FAMILY    LYMN-«ID^ 


89 


son !  (N.  Lat.  62°) .  We  have  it  from  Moose  Factor}' !  the  Slave 
River  25  miles  below  Peace  River !  Lake  Winnipeg !  the  Grand 
Rapids  of  the  Saskatchewan  River  !  and  hundreds 
of  more  southern  localities. 

The  variety  suhcrenatus  Carpenter  (Oregon, 
Nuttall)  occurs  in  British  Columbia  west  of  the 
Cascades  ;  being,  according  to  J.  K.  Lord,  replaced 
east  of  them  by  P.  binneyi.  We  have  it  from 
the  Puget  Sound  drainage !  Lake  La  Hoche ! 
and  Sumas  Lake,  B.  C. !  A  distorted  variety 
(^disjectus  Cooper)  is  reported  from  Lake  Tahoe, 
Calif.,  at  a  height  of  6,247  feet  above  the  sea. 
The  young  shell  was  described  from  Pueblo  Val- 
ley, Oregon,  by  Tryon  in  1865,  as  P.  oregonen- 
sis.  In  1870  Cooper  called  the  more  common  adult  (but  not  senile) 
form  P.  occidentalis  ^  and  later  confounded  it  with  the  Mexican  P. 
tumens  Cpr.,  and  gave  it  a  range  in  California  from  Kern  Lake, 
Tulare  Co.,  north  to  Puget  Sound,  and,  in  the  coast  drainage,  to  San 
Francisco   Bay.     There  is  a  doubt  as  to  whether  Planorbis  hornii 


Fig.  68.     Planor- 
bis trivolvis. 


Fig.  69.     Planorbis  trivolvis  var.  macrostomus  Whiteaves. 


Tryon  (1865),  from  "Fort  Simpson,  British  America,"  came  from 
Fort  Simpson  on  the  Mackenzie  River,  or  Fort  Simpson,  British 
Columbia  ;  but  the  figure  looks  more  like  the  Pacific  variety,  of  which 
it  is  probably  only  a  mutation.  We  have  specimens  from  various 
places  in  California,  and  Wallawalla,  Wash.,  labelled  P.  hornii  which 
are  merely  a  depauperate  form  of  suhcrenatus. 

On  the  other  hand,  from  the  Dall  River,  a  northern  affluent  of  the 
Yukon  in  Alaska,  in  N.  Lat.  66°,  we  have  the  typical  form  of  trivolvis 


90  LAND    AND    FRESH    WATER    MOLLUSKS 

Stretching  westward  with  the  Yukon  drainage  !  I  have  never  seen  any 
specimens  corresponding  exactly  to  Tryon's  figure  of  P.  hornii^  but 
the  variations  I  have  seen  of  P.  subcrenatus  often  approach  it  so 
closely  that  I  have  little  doubt  of  their  identity.  P.  macros totnus 
seems,  from  an  examination  of  the  types,  to  be  a  form  of  trivolvis 
which  has  survived  a  year  longer  than  usual,  in  a  locality  where  it  was 
not  stinted  in  lime,  resulting  in  a  remarkably  fine  shell  with  richly 
colored  aperture. 

Planorbis  (Planorbella)  campanulatus  Say. 

Planorbis  campanulatus  Say,  Journ.  Acad.  Nat,  Sci.  Phila.,  11,  p.  166,  Jan., 
1821  (Cayuga  Lake,  N,  Y.).  —  Haldeman,  Mon.  Limn.,  p.  9,  pi.  i, 
figs.  7-1 1,  1844. 

Planorbis  bellus  Lea,  1844  (immature  shell)  +  P.  complanatus  Miller  Christy, 
1885. 

Range.  —  The  type:  New  England  to  Tennessee,  Florida  and 
northward  ;  Anticosti  Island  !  Lake  Superior  to  the  Saskatchewan;  L. 
Winnipeg,  Red  River  of  the  North,  Nelson  and  English  Rivers ; 
Moose  Factory  !  Great  Slave  Lake,  N.  Lat.  62°  ;  Lake 
of  the  Woods  ! 

Variety  rudentis  :  Knee  Lake,  Hayes  River,  Kee- 
watin,  N.  Lat.  55°  (E.  A.  Preble)  ! 

This  well  known  species  is  confined  to  the  Atlantic, 
Mackenzie,  and  Hudson  Bay  watersheds,  and  has  not 

, .        '  been  reported  north  of  Great   Slave  Lake.     So  far 

orbts    campanu-  ^     , 

latus  Say.  ^^  '^'^  specimens  examined  go  to  show,  it  is  rather  re- 

markably uniform  in  its  characters,  the  number  of 
whorls  remaining  always  about  the  same,  though  the  actual  size 
varies  with  the  food  supply  and  healthfulness  of  the  environment. 

A  form  which  may  prove  distinct,  or  a  variety  of  this  species,  was 
collected  by  Mr.  Preble  at  Knee  Lake.  The  comparative  measure- 
ments are : 

Whorls.  Major  Diam.  Minor  Diam.  Axis. 

Type.  4.75  15.0  mm.  II  mm.  6.5  mm. 

Variety.  5.25  17.5  14  6.0 

Very  similar  specimens  were  obtained  from  Anticosti  Island  and 
from  Marl  Lake,  Michigan,  in  which  the  coil  is  even  more  irregularly 
wound,  a  condition  I  take  to  be  pathological.  The  most  noticeable 
difference,  after  the  axially  shorter  whorls  and  larger  size,  is  in  the 
umbilicus,  which  in  the  variety  is,  as  it  were,  reamed  out,  exhibiting 
three  and  a  half  whorls  ;  while  in  the  more  compact  type  the  umbilicus 
when  examined  with  a  lens  shows  only  two  and  a  half  whorls,  which 


FAMILY    LYMN^ID^  9I 

diminish  in  size  much  more  rapidly  than  in  the  variety.  The  campan- 
ulate  aperture  is  about  the  same  size  in  both  forms,  but  seems  larger 
in  the  type  because  the  rest  of  the  shell  is  so  much  more  tightly 
wound.  The  suture  on  the  apical  side  seems  deeper  and  wider  than 
in  the  type.  Nine  specimens  of  the  variety  were  obtained,  and  I  sug- 
gest for  it  the  name  rudentis^  from  the  similarity  of  the  whorls  to  a 
coiled  hawser. 

Planorbis  (Menetus)  ezacuous  Say. 

Planorbis  exacuous  Say,  Joum.  Acad.  Nat.  Sci.  Phila.,  II,  p.  168,  Jan.,  1 821 
(Lake  Champlain)  ;  Long's  Exp.  Rep.,  11,  p.  261,  1824. 

Planorbis  exacutus  Gould,  Inv.  Mass.,  p.  208,  fig.  137,  1841. — Haldemax, 
Mon.  Limn.,  p.  21,  pi.  iv,  figs.  1-3,  1844. 

Paludina  hyalina  Lea,  1839  (scalariform  monstrosity). 

Range. — Northern  United  States,  east  of  the  Rockies;  Canada, 
etc.,  south  to    New   Mexico. 

Lake  Superior  to  Lake  Winnipeg !  Manitoba  generally ;  Moose 
Factory,  Hudson  Bay  !  Left  bank  of  the  Yukon  below  Fort  Yukon, 
Alaska,  in  Pleistocene  marl  (A.  J.  Collier)  ! 

Variety  megas  Dall,  nov.  :  Birtle,  Manitoba  (R.  M.  Christy) . 

This  species  has  a  number  of  varieties  both  in  size  and  form.  The 
typical  shell  is  of  a  pale  brownish  horn  color,  with  a  somewhat  glisten- 
ing surface,  rather  rudely  striated  by  the  incremental  lines,  and  with 
faint,  almost  microscopic,  revolving  striae.  The  form  is  lenticular, 
coming  to  an  acute  angle  at  the  periphery.  In  1863  I  found  in  the 
vicinity  of  Marquette,  Michigan,  an  unusually  depressed  brownish 
variety  in  which  the  peripheral  keel  was  delicately  serrate.  In  the 
northwestern  part  of  its  range  the  tendency  is  for  the  species  to  become 
whitish  and  of  a  larger  size  than  the  average  New  York  or  New 
England  specimens.  This  reaches  its  maximum  in  specimens  col- 
lected in  Manitoba  by  Mr.  R.  Miller  Christy,  for  which  I  propose  the 
varietal  name  megas.     The  comparative  measurements  are  as  follows  : 


Whorls. 

Max.  Diam. 

Min.  Diam. 

Axis. 

Type. 

3-33 

4.7  mm. 

3.7  mm. 

I.o  mm, 

Variety. 

3-75 

7.8 

6.0 

2.0 

The  variety  is  of  a  slightly  milky  translucency ;  on  the  base  the 
whorl  is  more  or  less  impressed  within  the  peripheral  keel  and  the 
spiral  striation  is  much  more  marked  than  in  the  typical  form. 

Binney  has  united  with  this  species  Planorbis  lens  Lea,  1839  (not 
Brongniart,  1810)  =  P.  lenticularis  Lea,  1844  (not  Schlotheim, 
1818)  =  /*,  hrongniartiana  Lea,  1842  ;  but  an  examination  of  Lea's 


92  LAND    AND    FRESH   WATER    MOLLUSKS 

cotypes,  now  in  the  National  Museum,  makes  it  evident  that  Dr. 
Gould  was  right  in  referring  this  form  to  P.  dilatatus  Gould,  1841  (not 
Pfeiffer,  1841^),  or  dilatus  Haldeman,  1844.  To  this  latter  form,  in 
my  opinion,  should  be  united,  as  local  races,  P.  buchanensis  Lea, 
1844,  and  P.  alabamensis  Pilsbry.  The  young  of  P.  exacuous  Say 
frequently  approach  dilatatus^  but  the  latter  can  usually  be  distin- 
guished by  its  axial  height  being  greater,  its  columella  more  vertical, 
and  the  substance  of  the  shell,  especially  in  southern  specimens,  more 
thick  and  solid.  The  aperture  of  the  adult  dilatatus  is  usually  dis- 
tinctly thickened  by  a  deposit  of  callus,  but  in  exacuous  I  have  never 
observed  more  than  a  very  thin  wash  of  shelly  matter  around  the  open- 
ing. I  have  spelled  the  name  of  this  species  as  Say  did  in  two  sepa- 
rate works ;  as  he  gave  no  derivation  it  seems  to  me  we  have  no  right 
to  correct  his  spelling  on  purely  theoretical  grounds. 

Planorbis  (Menetus)  opercularis  Gould. 

Planorbis  opercularis  Gould,  Proc,  Boston  Soc.  N,  Hist.,  ir,  p.  212,  1847; 
Moll,  U.  S.  Expl.  Exp.,  p.  113,  Atlas,  figs.  132,  132,  a-<5,  1852  (Sacra- 
mento River,  Calif.). 
Planorbis  planulatus  Cooper,  Rep.  Nat.  Hist.  Wash.  Terr.,  p.  378,  1859  ; 
Pacific  R.  R.  Rep.,  xii,  p.  378. —  Binney,  Land  and  Fw.  Shells  N.  Am., 
pt.  II,  p.  126,  fig.  209,  1865. 

Planorbis  centervillensis  Tryon,  Mon.  Fr,  Univ.  Moll.  U.S., 

p.  57,  Planorbis,  pi.  vii,  figs.  7-9,  1872. 
Planorbis  opercularis  var.  oregonensis  Vanatta,  Nautilus, 
IX,    p.    53,    Sept.,    1895  ;  not  P.    oregonensis   Tryon, 
1865. 
Planorbis  callioglyptus  Vanatta,  Nautilus,  ix,  p.  54,  1895. 

Range. — San  Francisco  and  northward,  west  of  the 
Sierra  Nevada. 

Type  form :  California !  Oregon !  Washington 
near  Seattle ! 

Variety  flanulatus  W.  Cooper:  Whidbey  Island, 

Puget  Sound !  Shawnigan  Lake,  Vancouver  Island ! 

Fig.  71.  Plan-     Seattle,  Wash. !    Freeport,  Wash. !  Victoria,  B.  C. ! 

orbisopercularis  Campbell's  Creek,  B.  C. !  Pender  Island,  B.  C. ! 
Gould  (typical).  ^  .         '  .,     ,  t^  •     -r,       , 

Atka  Island,  Aleutians,  Alaska,  near  Korovm  Bay  ! 

Variety   centervillensis    Tryon :    Alameda,  Calif. !    Noyo   River, 

Calif. !  San  Leandro,  Calif. !  Oregon ;  Unalaska  Island,  Alaska  I 

Variety  oregonensis  Vanatta  :  Salem  and  Portland,  Oregon  ! 

^  I  learn  through  Prof,  von  Martens  that  Pfeiffer's  species  was  published  in 
the  double  part  v-vi,  of  the  Archiv  fur  Naturgeschichte,  either  in  the  last  part 
of  1841  or  the  earlj  portion  of  1842,  so  that  Gould's  priority  is  certain. 


FAMILY    LYMN-(EID^  93 

This  species  is  the  analogue  of  P.  exacuous  Say  on  the  Pacific 

Coast.     The  typical  form  from  the  Sacramento  River  and  the  vicinity 

of  San  Francisco  Bay  is  quite  lenticular,  with  the  periphery  marked 

by  a  (frequently  marginated)  keel.     The  shell  itself  is  pale  yellow  or 

white   under  a  rather  strong  periostracum,  which  is 

almost  invariably  more  or  less  discolored  by  deposits 

of  a  brown  or  black  color.     The  sculpture  is  like  that  \     ■  -i 

of   exacuous^    the   spiral   sculpture  being   faint    and        Fig.  72.  Plan- 

sometimes  absent  in  southern  specimens,  and  tending     orbts opercularts 

to  be  emphasized  in  northern  ones.     As  a  rule  the     ^   *  ^ 

.  .  .        Cooper, 

margin   of   the  aperture  is   not   thickened   except   in 

young  specimens  which  have  been  overtaken  by  drought  or  winter 
before  maturity.  The  keel  is  generally,  but  not  always,  present  in 
southern  shells,  but  those  from  Oregon  and  northward  show  a  tend- 
ency to  form  a  shell  either  without  a  noticeable  keel,  or  with  the  keel 
forming  a  margin  to  a  plane  upper  surface,  rather  than  a  median 
carina.  When  compared  with  Cooper's  types  in  the  National  Museum 
Mr.  Vanatta's  P.  callioglyptus  is  seen  to  be  identical.  The  variety  ore- 
gonensis  retains  the  typical  form  but  has  stronger  spiral  sculpture.  I 
regard  P.  centervillensis  of  Tryon  as  a  P.  flanulatus  with  the  keel 
obsolete.  What  appear  to  be  intergradational  forms  are  numerous  in 
the  large  series  of  the  National  Museum  ;  though  it  would  seem  incred- 
ible to  any  one  possessing  only  the  extremes  that  they  can  belong  to 
the  same  species. 

Planorbis  (Gyraulus)  hirsutus  Gould. 

f  Planorbis  albus  Muller,  Verm.  Terr,  et  Fluv.,  il,  p.  164,  1774. 

Planorbis  hirsutus  Gould,  Am.  Journ.  Sci.,  xxxviii,  p.    196,    1840;   Inv. 

Mass.,  p.  206,  pi.  XI,  fig.  135,  1841. 
Planorbis  borealis  (LovkN)  Westerlund,  Mai.  BL,  xxri,  p.  TJ,  1875. 

Range.  —  Washington,  D.  C.  !  northward,  east  of 
the  Mississippi.  Lake  Superior  !  Lake  of  the  Woods  ! 
Lake  Winnipeg  and  the  Saskatchewan  River  !  Great 

„  _,         Slave  Lake ! 

Fig.  73.  Plan- 
orbis hirsutus        ^^^'  ^orealis  Westerlund:  Port  Clarence,  Alaska. 
Gould,    f.  Northern  Sweden. 

This  species  appears  to  be  common  only  in  New 
England,  if  one  may  trust  reports,  and  it  is  remarkable  how  few 
records  there  are  of  it  in  the  literature  of  American  fresh  water  shells. 

The  shell  is  variable  in  form  ;  from  having,  in  what  I  have  re- 
garded as  the  type,  well  rounded  nearly  cylindrical  whorls,  it  varies  to 
a  form  more  or  less  depressed  and  carinate  and  with  an  oblique  aper- 


^  LAND    AND    FRESH    WATER    MOLLUSKS 

ture,  which,  when  it  has  lost  its  hispid  periostracum,  can  hardly  be 
distinguished  from  the  shell  which  is  usually  called  dejlectus  of  Say. 
This  latter  form,  which,  when  in  perfect  condition,  is  fully  as  hairy 
as  the  typical  hirsutus^  is  apparently  identical  with  the  shell 
which  European  writers  catalogue  under  the  name  draparnaudi 
or  draparnaldi  of  Sheppard.  In  its  best  state  this  has  a  peripheral 
fringe  of  longer  hairs  than  those  elsewhere  on  the  surface,  beneath 
which  is  usually,  but  not  always,  a  faint  peripheral  keel  like  that  of 
P.  dejlectus  Say,  which  is  distinguishable,  so  far  as  the  shell  is  con- 
cerned, only  by  its  less  profuse  and  hairy  periostracum.  I  should  not 
be  at  all  surprised  if  the  two  were  eventually  shown  to  be  extremes  of 
one  specific  form,  especially  as  I  have  been  unable  to  find  specimens  of 
typical  dejlectus  which  do  not  somewhere  exhibit  traces  of  spiral  stri- 
ation  like  that  of  P.  hirsutus.  The  identity  of  our  American  species 
with  the  so-called  P.  alhus  Muller,  of  Europe,  I  do  not  doubt,  but 
whether  the  name  albus  is  the  proper  one  to  use  for  the  latter  is  open 
to  question,  and  on  the  present  occasion  I  prefer  to  use  a  name  about 
whose  application  no  doubt  can  exist.  The  differences  which  have 
been  reported  to  exist  between  the  New  England  and  the  European 
shell  are  due  to  the  comparison  being  made  between  discrepant  varie- 
ties. If  a  series  including  all  varieties  from  many  different  localities 
in  Europe,  be  compared  with  a  similar  American  series,  parallels  for 
each  variation  will  be  found. 

Planorbis  borealis  (Loven  MS.)  Westerlund,  after  specimens  fur- 
nished by  Westerlund,  is  merely  a  somewhat  delicately  sculptured 
mutation  of  this  species. 

Planorbis  (Gyraulus)  deflectus  Say. 

Planorbis  deflectus  Say,  Long's  Exp.  Rep.,  ii,  p.  261,  pi.  xv,  fig.  8,  1824. — 
Haldeman,  Mon.  Limn.,  p.  25,  pi.  iv,  figs.  4-7,  1844 
(N.  W.  Territory). 

Planorbis  virens  Adams,  1840  ;  young  shell. 

Planorbis  obliquus  De  Kay,  1843. 

Range, — In  America  the  same  as  that  of  P.  hir- 

FiG.  74.  Plan-  , 

,.       ,  J,    .       sutus. 
orbts      deflectus  ■,    ,   -r    ■,         ,    ■,      -.tt       -y    ,    r^  01 

gg     2  Ottawa,  Canada  !  Lake  of  the  Woods  !  Great  Slave 

Lake  !  Dall  River,  Alaska,  Lat.  (>(i°  N, !  Popof  Island, 

Shumagins,  Alaska  (Kincaid)  ! 

Doubtfully  distinct  from  the  preceding  species.     It  differs  chiefly 

from  the  variety  draparnaudi  by  the  feebleness  or  absence  of  the 

hispidity  of  the  periostracum.     The  deflection  of  the  aperture  and  the 

consequent  form  of  the  mouth  of  the  shell  are  inconstant  characters, 


FAMILY    LYMN^IDvE  95 

although  they  have  been  called  '  characteristic  *  by  the  very  authors 
whose  evidence  shows  the  inconstancy. 

Planorbis  (Torqxiis)  parvus  Say. 

Planorbis  parvus  Say,  Nicholson's  Enc,  ist  ed.,  ii  (no  pagination),  pi.  i,  fig. 

5,  1817. —  Haldeman,   Mon.    Limn.,   p.    27,   pi.  iv,    figs.    19-23,    1844 

(Delaware  R.) — Binnev,  Land  and  Fw.  Sh.  N.  Am.,  il,  p.  133,  figs.  222- 

223  (not  224),  1865. 
Planorbis  concavus  Anthony,  MS.,  various  catalogues. 
Planorbis  elevatus  C.  B.  Adams,  Bost.  Joum.  N.  Hist.,  ill,  p.  327,  pi.  Ill,  fig. 

16,  1840  ;  young  shell  (S.  Boston). 
Planorbis  billingsi  Lea,  1866,  from  types  (Ottawa,  Canada). 

Range.  —  In  America,  the  whole  of  eastern  North  America  from 
Florida  to  N.  Lat.  67°,  and  the  Yukon  drainage  system. 

Ottawa,  Canada  !  northward  and  westward  to  Lake  Winnipeg !  the 
Saskatchewan  River !  Alberta  at  Laggan,  Olds  and  McLeod ;  Mani- 
toba at  Brandon  and  Birtle !  Methy  Lake ;  Moose  Factor^' !  Fort 
Simpson,  Mackenzie  River !  Lake  Bennett,  Yukon  Territory  !  Left 
bank  of  the  Yukon  below  Fort  Yukon,  Alaska  ! 

The  most  striking  characteristic  of  this  widespread  species  is  its 
'reamed  out'  umbilicus.  P.  limophilus  Westerlund,  its  nearest 
European  analogue,  may  be  distinguished  at  once  by  its  shallow  and 
flattish  umbilicus.  It  rarely  shows  any  trace  of  spiral  sculpture  and, 
when  clean,  is  brightly  polished.  In  the  last  whorl  of 
the  adult  the  portion  above  the  periphery  is  usually 
somewhat  flattened  or  obliquely  depressed. 

Planorbis  (Torquis)  vermicularis  Gould. 

Planorbis  vermicularis  Gould,  Proc.  Boston  Soc.  N.  Hist., 
II,  p.  212,  1847  ;  Moll.  U.  S.  Expl.  Exp.,  p.  112,  pi., 
figs.  131,  Or-b,  1852  (Oregon). 

Range. — Northern  California  !  Oregon  !   and  Van- 
couver Island,  British  Columbia ! 

On  comparison,  the  t3^e  of  P.  vermicularis  is  seen 

to  have  vertically  deeper  whorls  than  a  specimen  of  P.  i ' 

parvus  of  the  same  number  and  diameter.  The  aper-  Fig.  75.  Plan- 
ture  is  more  expanded,  and  much  larger,  as  one  °^^"  vennicu- 
would  expect  from  the  greater  lumen  of  the  whorl.  '^!'1^Z.  '  ''"^^ 
Specimens  from  middle  and  southern  California  have 
a  different  aspect  and  may  prove  on  more  careful  study  to  belong  to  P. 
parvus.  They  certainly  do  not  agree  with  the  Oregon  shell,  which, 
however,  I  have  seen  from  Noyo,  California. 


96  LAND    AND    FRESH    WATER    MOLLUSKS 

Planorbis  (Torquis)  nathorsti  Westerlund. 

Planorbis  na//iors/iW esteklvhd,  Vega  Expd.,  iv,  p.  168,  1887.  —  Posselt, 
Consp.  Fauna  Gronl.  Moll.,  p.  162,  1898. 

Aulatsivik,  West  Greenland  (Sofia  Expedition)  ;  Labrador  (Storer). 

This  species  is  said  to  approach  I^.  arch'cus,  but  has  four  and  a 
half  turns  in  a  diameter  of  3.5  mm.,  while  the  latter  turns  only  three 
and  a  half  times  in  5.0  mm.  I^.  nathorsti  has  spiral  as  well  as  trans- 
verse striation.     It  has  not  been  figured. 

Some  specimens  in  the  National  Museum  collected  in  Labrador  ex- 
hibit about  four  turns  in  3.5  mm.  diameter,  according  to  my  calcula- 
tion, but  so  much  personal  equation  enters  into  the  estimation  of  the 
extent  of  the  first  whorl  that  I  am  inclined  to  think  they  belong  to 
Westerlund's  species,  in  which  case  it  is  intermediate  between /arz^wj 
and  arcticus^  but  without  the  excavated  umbilicus  of  the  former. 

Planorbis  (Torquis)  arcticus  Moller. 

Planorbis  arcticus  (Beck,  MS.)  Moller,  Index  Moll.  Gronl.,  p.  5,  1842. — 
MoRCH,  Am.  Journ.  Conch.,  iv,  p.  32,  pi.  iv,  fig.  9,  1868. — Morch,  in 
Rink's  Danish  Greenland,  p.  436,   1877. 

Range.  —  West  Greenland  !    Fort  Chimo,  Ungava,  Labrador  ! 

Species  with  larger  whorls,  the  last  more  expanded  near  the  aper- 
ture, and  with  the  sides  of  the  umbilicus  not  excavated  as  in  P.  parvus 
Say. 

Planorbis  (Torquis)  umbilicatellus  Cockerell. 

Planorbis   umbilicaius  Taylor,  Journ.  Conch.,  iv,  p.  351,  1885  ;  not  of  Mul- 

ler,  1774.     Manitoba. 
Planorbis  wnbilicatellus  CocKKR.E\A^,  Conch.  Exch. ,  li,  p.   68,  Nov.,  1887. — 

Vanatta,  Nautilus,  ix.  No.  10,  p.  117,  1896. 

Range.  —  From  Mesilla,  New  Mexico  !  northward,  through  Col- 
orado, Montana,  Iowa,  Minnesota,  to  Manitoba. 

Rapid  City,  Birtle,  Brandon !  in  Manitoba ;  McLeod,  Red  Deer, 
Olds,  Laggan,  in  Alberta. 

Planorbis  (Armiger)  crista  Linn^. 

Nautilus  crista  Linn6,  Syst.  Nat.,  ed.  x,  p.  709,  1758. 
Turbo  nautileus  Linn6,  Syst.  Nat.,  ed.  xii,  p.  1241,  1767. 
Planorbis  imbricatus  Muller,  Hist.  Verm.  Terr.,  li,  p.  165,  1774- 
Planorbis  cristatus  Draparnaud,  Hist.,  p.  44,  pi.  il,  figs.  1-3,  1805. 
Planorbis  nautileus  Gray,  Turton's  Man.   Land  and  Fw.   Shells,  p.    236,  pi. 

VIII,  fig.  94,  1857. 
Planorbis  costatus  De  Tar  and  Beecher,  leaflet  of  one  page,  Albany,  Oct. 

25,  1878. 
Planorbis  crista  Woodward,  Brit.  Nonmarine  Moll.,  in  Journ.  Conch.,  x,  p. 

355.  1903- 


FAMILY    LYMN^ID^  97 

Range.  —  Europe,  Algeria,  in  the  Old  World ;  in  America  at  Cari- 
bou, Aroostook  Co.,  Maine!  Hamilton  and  Ottawa,  Canada;  Ann 
Arbor,  Michigan  !  Red  Deer  in  Alberta  ;  Manitoba. 

This  small  and  inconspicuous  species  will  doubtless  be  found  in 
many  other  localities  when  thorough  search  is  made. 

Genus  Segmentina  Fleming. 

Segmentina  Flemijjg  (1817,  Edin.  Encycl.,  ed.  vii,  vol.  xil,  fide  Turton 
Manual,  p.  116,  1831)  ;  Brit.  An.,  p.  279,  1828.  Ty^c  Nautilus  lacusiris 
(Lightfoot)  Montagu.  —  Haldeman,  Men.  Limn.,  iv,  p.  14,  1842. — 
Stein,  Schnecken  u.  Musch.  Berlins,  p.  78,  1850. — Westerlund, 
Fauna  Pal.  Reg.,  v,  p.  85,  1885. — Woodward,  List  Bnt.  Nonmarine 
Moll.,  p.  355,  1903. 

Hemithalamus  Leach  (18 19),  Proofsheets,  p.  137,  _/f</<f  Turton,  Manual,  p. 
116,  1831.  —  Fitzinger,  Syst.  Verz.,  p.  no,  1833.  —  Rossmassler, 
Icon.,  \,  pt.  II,  p.  15,  1835. — H.  nitidus  (Muller)  Leach  =  P.  Hneatus 
JefTreys. 

5<gw^«/d:rfa  SwAiNSON,  Malac,  p.  337,  1840  ;  lapsus  pro  Segmentina  Fleming. 

Hippeutis  (sp.)  Agassiz  in  Charpentier,  Fauna  Helvetica,  p.  22,  1837. — 
Hartmann,  Syst.  Uebers,  tab.,  1840. 

Dentatus  Gray,  P.  Z.  S.,  1847,  p.  181,  not  of  Beck,  1837,  P.  armatus  Gray  ; 
?:=/•.  amiigerus  Say  +  P'  armiger  Beck. 

'^  Planorbula  Haldeman,  Mon.  Limn.,  iv,  p.  14,  1842,  P.  armigerus  Sziy. 

Discus  Haldeman,  Mon.  Limn.,  i,  p.  4  of  cover,  July,  1840  (/*.  amiigerus 
Say),  not  of  Fitzinger,  1883. 

This  genus  w^as  founded  by  Fleming  on  the  Planorbis  nitidus  of 
Muller,  of  which  lacustris  Lightfoot,  is  a  synonym.  I  have  not  been 
able  to  verify  the  reference  to  the  Edinburgh  Encyclopedia.  Leach's 
name  was  circulated  in  proof  sheets,  but  not  actually  published  or  cited 
by  other  authors  until  after  Fleming's  description  appeared.  Beck  called 
a  group  of  Planorbes  '•Dentati'  but  applied  no  name  to  the  group, 
and  the  transformation  by  Gray  to  '  Dentatus^*  as  if  it  had  been  in- 
tended for  a  generic  or  subgeneric  name,  seems  quite  unwarranted. 

The  genus  may  be  divided  into  three  groups  as  follows  : 
Subgenus  Segmentina  s.  s.     Base  flattened,  coil  close,  margin  of  the 
aperture  simple,  sharp ;  lamellae  ridgelike,  several  sets  persistent  in 
the  adult.     Type  P.  nitidus  Muller.     Palearctic  region. 
Subgenus  Planorbula  Haldeman.     Whorls  rounded,  coil  loose,  mar- 
gin of  the  aperture  simple,  sharp,  slightly  expanded ;  lamellae  denti- 
form, only  one  set  persistent  in  the  adult.     Type,  P.  armigerus 
Say.     Nearctic  region. 
Haldemanina  Dall,  n.  sect.,  whorls  carinate  above  and  below,  margin 
of  aperture  thickened  and  reflected ;  lamellae  complex,   dentiform 
and  ridgelike,  one  series  persistent  in  the  adult.     Type,  Planorbis 
ivheatleyi  Lea.     Coosa  drainage  of  Alabama. 


98  LAND    AND    FRESH   WATER    MOLLUSKS 

The  lamellation  of  Segmentina  is  composed  of  irregular  undulate 
ridges,  radiating  from  the  axis  of  the  shell.  In  Planorbula  there  are 
four  dentiform  lamellae  on  the  outer  and  two  (one  quite  small)  on  the 
axial  side  of  the  throat,  in  a  general  way  mostly  turned  in  the  direction 
of  the  coil,  and  the  earlier  series  are  absorbed  as  the  animal  grows. 
The  position  and  shape  of  these  lamellae  are  remarkably  uniform  in  all 
the  species.  In  Haldemanina  the  lamellae  are  more  elongate  and  com- 
plex, requiring  a  diagram  to  define  their  relations,  but  on  the  whole 
more  like  Planorbula  than  Segmentina.  (See  Binney,  Land  and  Fw. 
Sh.  N.  Am.,  II,  p.  137,  figs.  226-7,  1865.) 

Segmentina  (Planorbula)  armigera  Say. 

Planorbis  armiget^s  Say,  Journ.  Acad.  Nat.  Sci.  Phila.,  11,  p.  164,  1818. — 
Haldeman,  Mon.  Limn.,  p.  30,  pi.  iv,  figs.  11-13,  1844. —  Gould,  Inv, 
Mass.,  p.  205,  fig.  138,  1841.     Type  locality,  Upper  Missouri. 

Planorbis  anniger  ^^CK,  Index,  p.  123,  1838. 

Range.  — New  England  and  the  Middle  States,  south  to  Georgia, 
westward  to  Nebraska,  and  northward  to  Great  Slave  Lake. 

Lake  Winnipeg  and  the  Saskatchewan  River !  Egg  Lake,  Saskat- 
chewan :  Red  Deer*  Battle  River;  Great  Playgreen  Lake,  Manitoba; 

Fort    EUice  and  Fort  Felly;  Ver- 

^  milion     Lake ;      Moose    Factory- ; 

(     ^        ^1  ^^^  James  Bay !  Fort  Resolution,  Great 

^-y  — !(2/  Slave  Lake ! 

Fig.  76.  Planor-  Fig.  77.  Teeth  Shell  biconcave,  of  five  whorls, 
btila  armigera  Say.     of    P.  -wheatleyi     polished,  with  an   ollvaceous   peri- 

rt,  nat.  size ;  3,  teeth     Lea,     for    com-         ,  _£  t   Ui.i 

.^      '    '  .  ostracum ;   upper    surface    slightly 

magnified.  parison.  .  o      j 

concave  in   the   center,    the  suture 

deep  but  not  channelled,  upper  surface  of  the  whorls  with  an  obscure 
carlnatlon,  the  last  part  of  the  last  whorl  expanded  and  suddenly  de- 
flected downward,  base  with  a  steeply  funicular  umbilicus,  exhibiting  In 
scalar  fashion  all  the  whorls,  and  bordered  by  an  obtuse  carina ;  peri- 
phery of  the  whorls  median,  rounded  ;  lip  simple,  hardly  thickened,  con- 
tinued across  the  body  by  a  thin  callus  ;  aperture  at  an  angle  of  45°  to 
the  vertical  axis  ;  surface  sculptured  by  fine  lines  of  growth  and  obso- 
lete microscopic,  inconstant,  spiral  striation.  Max.  diam.  8.0 ;  min. 
diam.  6.5  ;  height  3.0  mm. 

This  common  species  extends  well  to  the  north,  but  has  not  yet  been 
reported  from  any  part  of  the  Pacific  drainage,  where  it  appears  to  be 
replaced  by  a  very  similar  species,  P.  declivis  Tate,  which  however  has 
not  yet  been  collected  north  of  the  Umpqua  River,  Oregon,  specimens 
from  that  locality  and  from  Nicaragua  being  in  the  National  Museum. 


FAMILY    PHYSID^  99 

Segmentina  (Planorbula)  christyi  n.  sp.     Plate  ii,  figs.  lo,  ii. 

Shell  resembling  P,  armigera  in  a  general  way  but  having  six 
whorls,  the  upper  surface  nearly  flat,  the  latter  part  of  the  last  whorl 
in  nearly  the  same  plane  as  the  preceding  whorls,  with  no  marked 
deflection ;  the  whorls  rounded,  with  no  carina  above  or  below ;  the 
surface  sculptured  with  fine  close  silky  incremental  lines  and  fine  sharp 
spiral  striae,  giving  a  minutely  reticulate  effect  when  magnified  ;  aper- 
ture-plane about  25°  from  the  vertical ;  teeth  very  similar  in  form  and 
position  to  those  of  P.  armigera.  Max.  diam.  10. o;  min.  diam.  7.5  ; 
height  3.0  mm. 

High  Bluff,  Manitoba  !  (R.  Miller  Christy)  ;  Fort  Smith,  Mackenzie 
River  !  (E.  A.  Preble) . 

After  comparing  these  shells  with  a  large  series  of  P.  armigera  and 
finding  nothing  intermediate,  I  conclude  that  this  form  is  worthy  of  a 
name.  I  have  examined  seven  specimens  of  P.  christyi^  and  several 
hundred  from  forty  different  localities,  north  and  south,  of  P,  armi- 
gera. The  present  form  is  the  largest,  flattest,  and  most  sharply 
sculptured  of  the  group. 

Family  PHYSIDiE. 
Genus  Physa  Draparnaud. 

</%^^aDRAPARNAUD,  Tableau,  pp.  31,  52,  1801  ;  Hist,  des  Moll,  de  France, 
pp.  25,  28,  54,  1805;  first  species  Bulla  fontinalis  Linne.  —  Roissv, 
Moll.,  V,  p.  343,  1805. —  Studer,  Syst.  Verz.,  p.  25,  1820. —  Lamarck, 
An.  s.  Vert.,  vi,  pt.  2,  p.  155,  1822.  Not  of  Fitzinger,  1833,  norWes- 
terlund,  1902. 

Enydra  Hubner,  Zwei  Briefe,  18 10  (nomenclature  non-Linnean  ?). 

Physa  SowERBY,  Genera,  fasc.  vii  {LimncEa),  1822. —  Fleming,  Brit.  An. 
p.  276,  1828. —  Leach,  Proofsheets,  p.  150,  fide  Turton,  Man.,  p.  127, 
1831. —  Leach,  Synops.  Moll.  Gt.  Brit.,  p.  109,  1852. 

Rivicola  Fitzinger,  Verz.  Conch.,  p.  no,  1833.     Type  B.  fontinalis  Linne. 

<^Physa  BiNNEY,  Land  and  Fw.  Sh.  N.  Am.,  11,  p.  75,  1865. —  Dall,  Ann, 
Lye.  N.  H.  N.  Y.,  ix,  p.  355,  1870.     Type  P.  fontinalis. 

Phy sella  Haldeman,  Men.  Limn.,  i,  pp.  14,  38,  1842  ;  type  P.  globosa 
Hald. —  Dall,  op.  cit.,  p.  355,  1870. 

Physodon  Haldeman,  Men.  Limn.,  i,  pp.  14,  39,  1842;  type  P.  microstoma 
Hald.  —  Dall,  op.  cit.,  p.  356,  1870. 

?  Diastropha  Gray,  in  Turton,  Man.,  ed.  11,  p.  16,  1840;  sole  ex.  Physa 
contorta  Michaud. —  Haldeman,  Mon.  Limn.,  in,  3d  page  of  cover, 
1841,  text,  pp.  14,  35,  1842. — MoQUiN  Tandon,  Hist.  Moll.  Fr.,  11,  p. 
450,  1855. 

f  Diastropha  'Guilding,'  Gray  (Synops.  Brit,  Mus.,  1840,  fide  Agassiz), 
P.  Z.  S.,  1847,  p.  180;  Physa  guildingii  Syvz-insoTi. 

<^Phyza  Risso,  Hist.  Nat.  Eur.  Men,  iv,  p.  96,  1826;  .st  sp.  P.  fontinalis 
Drap. 

'yMacrophysa  Meek  (MS.  1865),  Dall,  Ann.  Lye.  N.  H.  N.  Y.,  ix,  p.  356, 
1870  ;  type  Physa  columnaris  Deshayes,  Eocene. 


lOO  LAND   AND   FRESH   WATER   MOLLUSKS 

"^Costatelia  Dall,  Ann.   Lye.  N.  H.  N.  Y.,  ix,  p.   355,  1870.     Type  Physa 

costata  Newcomb. 
'^Costella  Meek,  Inv.  Fos.  Upper  Missouri,  pp.  603-604,  1876  ;  lapsus  pro 

Costatella. 
'^Macrophysa  Tryon,  Struct.  Syst.  Conch.,  iii,  p.  103,  1884. 
.ff«//«a^  Westerlund,  Fauna  Pal.  Reg.,  p.  54,  1885  (not  of  Adanson,  1757)  ; 

Acta  Acad.  Sci.  Slav.  Merid.,  Zagrabiae,  cli,  p.  119,  1902. 
<^Buninus  Oken,  Lehrb.   d.  Naturg.,  sp.  x,  302-3,  181 5.     B.  fontinalis  L., 

first  species. 

This  genus  has  suffered  from  its  resemblance  to  the  sinistral  Lym- 
naeas  and  the  physiform  Planorboids,  which  have  been  and  still  are 
frequently  confounded  with  the  true  Physas.  Not  until  much  more  is 
known  of  the  dentition  and  soft  parts  will  it  be  practicable  to  eliminate 
from  Physa  all  the  unrelated  species.  The  group  containing  Isidora^ 
Physopsis^  etc.,  is  chiefly  South  European  and  African,  but  it  is 
probable  that  some  of  the  subtropical  American  species  also  belong  to 
it.  The  subgenus  Phy sella  Haldeman,  was  proposed  because  the 
author  believed  it  to  be  branchiate  instead  of  pulmonate,  but  we  now 
know  that  undoubted  species  of  Lymncea^  having  no  access  to  the 
atmosphere,  live  in  the  deep  waters  of  some  of  the  Swiss  lakes,  per- 
haps gathering  up  globules  of  oxygen  freed  by  aquatic  plants ;  and 
unless  some  more  definite  observations  show  anatomical  distinctions 
(such  as  were  merely  surmised  by  Haldeman)  the  group  is  hardly 
worth  retention.  Physodon  Haldeman,  so  far  as  the  shell  is  concerned, 
differs  from  Physa  s.  s.  only  by  an  almost  imperceptible  thickening 
below  the  obscure  plait  on  the  pillar,  and,  in  default  of  other  charac- 
ters, might  well  be  dispensed  with. 

The  soft  parts  of  Diastropha  contorta  (Mich.)  have  not  been  de- 
scribed, and  there  is  some  reason  to  think  it  may  be  an  Isidora.  Gray, 
who  first  introduced  it  in  connection  with  the  above  mentioned  species, 
subsequently  listed  it  as  a  name  (MS. .?)  given  by  Guilding,  and  men- 
tioned as  type  Physa  guildingi  Swainson,  which  is  an  Aplexa, 

The  groups  into  which  the  genus  may  confidently  be  divided  are  as 
follows  : 

Section  Physa  s.  s.  Shell  sinistral,  ovoid,  polished,  with  a  spire  shorter 
than  the  length  of  the  aperture,  an  obscure  plait  on  the  pillar,  with 
the  pillar  merging  gradually  into  the  peristome,  the  outer  lip  sharp, 
often  with  a  slight  thickening  internally,  the  inner  lip  closely 
appressed  to  the  body  and  pillar,  a  very  small  or  no  umbilicus,  the 
surface  of  the  shell  smooth  or  microscopically  striated.  Type  Bulla 
fontinalis  Linn^.  Holarctic  and  Temperate  regions  of  both  hemi- 
spheres, also  Hawaii. 


FAMILY    PHYSIDvE  lOI 

?  Section  Macrophysa  Meek.  Shell  elongate,  columnar,  large,  the 
last  whorl  and  aperture  small  compared  with  that  of  the  typical 
Physa^  the  surface  axially  striated.  Type  Physa  columnaris 
Deshayes,  Eocene  of  Paris  Basin. 
Section  Costatella  Dall.  Shell  physiform,  polished,  sculptured  with 
axial  ribs.     Type  Physa  costata  Newcomb. 

The  section  Macrophysa  has  been  affiliated  to  Isidora  by  Sandberger 
and  others,  but  as  the  species  is  only  known  in  the  fossil  state  some 
doubt  must  remain  as  to  its  relations.  It  has  somewhat  the  form  of 
Isidora  ivahlbergi  Krauss  from  South  Africa,  but  the  resemblance 
may  be  merely  a  parallelism  and  not  an  indication  of  relationship,  as 
we  find  several  species  of  Isidora  absolutely  indistinguishable  from 
true  Physa  except  by  anatomical  examination. 

The  groups  known  as  Ameria  Adams,  Glyptophysa  Crosse,  Plesio- 
physa  Crosse  and  Fischer,  Physopsis  Krauss,  Pulmobravchia  Pelsen- 
ear,  etc.,  are  more  or  less  intimately  connected  with  Isidora  Ehrenberg 
{Bulinus  Adanson)  and  do  not  form  part  of  the  family  Physidce. 
None  of  them  occurs  in  the  region  to  which  this  paper  relates.  I  am 
indebted  to  the  discussion  of  American  Physae  by  O.  A.  Crandall  in 
the  Nautilus,  volume  xv,  for  assistance  in  determining  the  species  of 
Physa  from  the  north. 

Physa  heterostropha  Say. 

Physa  heterostropha  Say,  Nicholson's  Encycl.,  Am.  ed.  (no  pagination),  pi. 

I,  fig.  6,  1817. —  Haldeman,  Men.  Lunn.,  p.  23,  pi.  11,  figs.  1-9,  1843. 

— BiNNEY,  Land  and  Fw.  Sh.  N.  Am.,  11,  p.  84,  figs.  144-5,  1865. 
Physa  piicata  De  Kay,  fragilis  Mighels,  lata  Tryon,  pritneana  Tryon,  and 

philippU  Kuster,  are  said  to  be  synonymous  by  Crandall. 

Range.  —  From    the   Potomac   and    Ohio   Rivers 
northward,  and  westward  to  the  Mississippi. 

Anticosti    Island !    Manitoba,   Red   River   of  the 

North,  Lac  des  Mille  Lacs  to  Lake  of  the  Woods ; 

Alberta,  at   Olds,  McLeod  and  Red  Deer.     Grand     ,  ,       .'-, 

'  '  heterostropha. 

Rapids  of  the  Saskatchewan  !  L.  Winnipeg  !  English 
River !    Albany  River !    near  James  Bay ;   Hudson  Bay  drainage  in 
Keewatin  at  Moose  Factory  !  and  Nelson  River  !  Lake  Isle  Lacrosse  ! 
Peace  River  !  and  Great  Slave  Lake  ! 

Readily  recognizable  by  its  form  and  the  absence  of  microscopic 
spiral  sculpture.  The  northern  specimens,  when  dead,  are  of  a  beau- 
tiful opalescent  white  with  a  claret  colored  apex. 

Physa  gyrina  Say. 

Physa  gyrina  Say,  Joum.  Acad.  Nat.  Sci.  PhUa.,  11,  p.  171,  1821.  — Halde- 
man, Men.  Limn.,  p.  32,  pL  3,  figs.  1-6,  1843  ;  Council  Bluffs,  Iowa. 


I02 


LAND    AND    FRESH    WATER    MOLLUSKS 


Fig.  79.  Physa 
gyrina  var.  hild- 
rethiana  Lea. 


Physa  hildrethiana  Lea,  oleacea  Tryon,  and  albofilata  Ancey,  are  united  by 

Crandall  with  this  species. 
Physa  fontinalis  J.  de  C.  Sowerby  (in  Richardson),  not  of  Linne. 

Range. — The  United  States  east  of  the  Mississippi, 
Canada,  and  northward. 

Manitoba !  Lower  Saskatchewan  near  Lake  Win- 
nipeg !  York  Factory,  Keewatin ;  Great  Slave  Lake  ! 
Methy  Lake  to  Great  Bear  Lake  (Richardson). 
Variety  oleacea  Tryon,  also  variety  hildrethiana 
Lea  :  Great  Slave  Lake  ;  Port  Clarence,  Alaska  (Bean) . 
This  is  the  prevalent  species  over  the  north  country, 
extending  to  the  Arctic  Circle  at  Great  Bear  Lake, 
and  westward  to  Bering  Strait.  It  is  to  be  noted 
however  that  Physa  in  this  region  is  nowhere  a  common  form  like 
Lymncea  or  Planorbis  ^  or  even  Aplexa,  The  varieties  noted  differ 
from  one  another  and  from  the  typical  form  chiefly  in  the  character 
of  slenderness. 

Physa  ancillaria  Say. 

Physa  ancillaria  Say,    Joum.   Acad.   Nat.   Sci.   Phila.,    v,    p.    124,  1825. — 

Haldeman,  Men.  Limn.,  p.  27,  pi.  iii,  figs,  i-io,  1843,  — Gould,  Inv. 

Mass.,  p.  213,  fig.  142,  1841, — Crandall,  Nautilus,  xv,  No.  4,  p.  42, 

1901. 
Physa  vinosa  GouLD,  and  P.  crassa  Walker,  are  regarded  as  subspecies  of 

P.  ancillaria  by  Crandall,  and  Binney  unites  with  it  P.  obesa  De  Kay. 

Range.  — The  United  States  northward  from  the  Potomac  and  Ohio 
Rivers,  and  east  of  the  Mississippi,  to  the  Saskatchewan.  Variety 
vinosa  Gould,  Lake  Superior. 

Manitoba.  Lake  of  the  Woods;  Lake  Winnipeg;  and  the  lower 
Saskatchewan  River. 

The  above  localities  are  cited  from  the  literature ;  I  have  seen  no 
specimens  from  north  of  the  United  States,  west  of  Ontario. 

Physa  lordi  Baird. 

Physa  lordi  Baird,   Proc.   Zool.   Soc.   London,  for  1863,  p. 

Land  and  Fw.  Sh.  N.  Am.,  11,  p.  76,  figs.  125-127. 
Physa  parkeri  Currier,  in  Decamp,  List  of  Shellbearing 

Moll,  of  Mich.,   Kent  Sci.  Inst.  Misc.  Pub.,  v,  p.    15, 

pi.  I,  fig.  3,  1881. 

Range.  —  Washington  and  British  Columbia,  east 
of  the  Cascade  Mountains,  eastward  to  the  northern 
peninsula  of  Michigan,  and  southward  at  high  alti- 
tudes to  New  Mexico. 

Round  Lake  !  Lake  Houghton  !  and  Lake  Douglas  !  pj^  g^  pftysa 
northern  Michigan  !  Mingusville,  Montana  !  Ft.  Col-     lordi  Baird. 


68.  —  Binney, 


FAMILY    PHYSID^  IO3 

ville,  Wash. !  Lake  Osoyoos,  Lat.  49°  and  Kootenai  Lake,  British 
Columbia;  San  Rafael,  Valencia  Co.,  New  Mexico;  altitude  6,000 
feet! 

I  find  this  remarkable  species  in  the  National  collection  labelled  P. 
parkeri  Currier.  There  is  a  form  very  similar  in  miniature  to  this, 
which  occurs  in  the  Gila  River,  Arizona,  and  elsewhere  in  tliat  region, 
but,  while  this  may  be  a  dwarf  form  of  P.  lordi^  I  do  not  feel  suffi- 
ciently certain  to  include  it  in  the  range  of  the  latter.  The  Michigan 
specimens  however  are  typical,  and  finely  developed,  not  in  any  way 
to  be  distinguished  from  those  collected  in  Washington. 

Physa  propinqua  Tryon. 

Physa propinqua  Tryon,  Am.  Joum.  Conch.,  i,"p.  223,  pi.  23,  fig.  5,  1865  ; 
Mon.  Fw.  Univ.,  Moll.  U.  S.,  pt.  3,  p.  132,  pi.  vi,  fig.  13,  1872. 

Range. — Jordan  Creek,  SW.  Idaho,  west  to  Puget  Sound  and 
south  to  Los  Angeles,  Calif. 

Puget  Sound  drainage  !  Sumas  Prairie,  Fraser  River  valley,  British 
Columbia,  and  elsewhere  in  the  lowlands  of  British  Columbia,  east  of 
the  Cascades. 

This  form  closely  resembles  P.  heterostropha  Say,  and  is  the  shell 
which  has  been  listed  by  that  name  from  the  Pacific  Coast,  where  ac- 
cording to  Tryon  and  Crandall  the  true  P.  heterostropha  does  not 
occur.  Whether  it  is  a  distinct  species,  or  a  special  mutation  of  P. 
ampullacea  Gould,  or  a  western  race  of  some  other  species,  I  do  not 
feel  able  to  determine,  and  so  I  accept  Tryon's  assurance  that  it  is  a 
valid  species. 

Physa  ampullacea  Gould. 

Physa  bullata  Gould,   Proc.  Boston  Soc.  N.   Hist.,  v,  p.    128,  1855  ;  not  of 

Potiez  et  Michaud,  1838. 
Physa  ampullacea  Gould,  in  Binney,   Land  and  Fw.  Sh.  N.  Am.,  11,  p.  79, 

figs.  134,  135  (not  133),  1865. 

Range.  —  Oregon  and  Washington,  northward  to  Norton  Sound  on 
the  Pacific  Coast. 

Oregon  !  Lake  Oyosa,  Washington  !  Vancouver  Island,  near  Vic- 
toria ;   ponds  near  St.  Michael,  Norton  Sound,  Alaska,  rare  ! 

A  single  specimen  of  what  seems  to  be  this  species  was  found  among 
other  shells  collected  near  St.  Michael,  Alaska,  by  E.  W.  Nelson. 

Physa  (Aplexa?)  hordacea  Lea. 

Physa  hordacea  Lea,  Proc.  Acad.  Nat.  Sci.  Phila.,  for  1864,  p.  116;  Joum. 
Acad.  Nat.  Sci.  Phila.,  (2),  vi,  pp.  176,  177,  pi.  xxiv,  fig.  102,  1866; 
Obs.  Gen.  Univ.,  xi,  pp.  132-3,  pi.  xxiv,  fig.  102,  1866. 


I04  LAND    AND    FRESH    WATER    MOLLUSKS 

Bulinus  hordaceus  Tryon,  Mon.  Fw.  Univ.  Moll.  U.  S.,  p.   170,  pi.  vii,  fig. 
19,  1872. 

Range.  —  Oregon,  Washington,  Vancouver  Island. 

Fort  Vancouver,  Wash. !  near  Puget  Sound,  Wash.  ! 

This  is  the  small  species,  having  much  the  appearance  of  an  Aplexa., 
which  has  been  cited  on  the  authority  of  Dr.  J.  G.  Cooper  as  Aplexa 
hypnorum  from  near  Puget  Sound.  This  error  vs^as  afterward  cor- 
rected by  Cooper  himself.  No  observations  have  been  recorded  in 
regard  to  the  animal,  and  when  these  have  been  made  it  is  entirely  pos- 
sible that  the  creature  may  turn  out  to  be  an  Aplexa.  It  is  entirely 
distinct  from  A.  hypnorutn  at  any  rate 

Genus  Aplexa  Fleming. 

Bulla  (sp.)  Linn6,  Syst.   Nat.,  ed.  x,  p.  727,  1758. — Gmelin,  Syst,  Nat.,  vi, 

p.  3428,  1792. 
Planorbis  (sp.)  O.  T.  Muller,  Hist.  Verm.,  11,  p.  169,  1774. 
7«r(5<7  (sp.)  Walker,  Test.  Min.  var.,  p.    15,  1787. 
<^Bulinus  O.  T.  Muller,  in  Der  Naturforscher  (Halle),  xv,  p.  6,  1781  (after 

Adanson,  Senegal,  p.  5,  1757,  non  binomial). 
<iPhysa  Draparnaud,  Tableau,  pp.  31,  52,  1801  ;  Hist,  des  Moll,  de  France, 

p.  55.  1805. 
<iBulifnus  PoiRET,  Coq.  Fluv.  et  Terr.,  p.  41,  1801  ;  not  of  Scopoli. 
<^Bullinus  Oken,  Lehrb.  d.  Naturg.,  pp.  x,  302,  181 5. 
Aplexa  Fleming,  in  Sowerby,  Gen.,  fasc.  vii,  1822  ;  Hist.  Brit.  An.,  p.  276, 

1828.     Ty^Q  Bulla  hypnorutn  Uirmt,  1758. 
<iPhyza  Risso,  Hist.  Nat.  Eur.  Men,  iv,  p.  96,  1826. 
Nauta  (Leach,  MS.)  Turton,  Man.,  p.  129,  1831  (in  syn.). — Leach,  Syn. 

MolL  Gt.  Brit.,  p.  no,  1852. 
<^  Bulinus  Beck,  Index  Moll.,  p.  116,  1838  ;  not  Bulinus  Beck,  op.  cit.,  p. 

117,  nor  Philippi,  Handb.  Conch.,  p.  255,  1853. 
Pkysa  FiTZlNGER,  Syst.  Verz.,  p.  110,  1833  ;  not  of  Draparnaud. 
AplexusGKK'i,  Turton's  Man.,  ed.   11,  p.   255,  1840. —  Sowerby,  Man.,  ed. 

II,  p.  70,  1842. —  Brown,  111.  Conch.  Gt.  Brit.,  p.   135,  1844. — Chenu, 

Man.,  I,  p.  481,  1859. 
Aplexa'R^cvi,  Index  Moll.,  p.  116,  1838.  — Philippi,  Handb.  Conch.,  p.  255, 

1853.  — MoRCH,  Vidensk.  Meddel.,  p.  308,  1864.  — Tryon,  Struct.  Syst. 

Conch.,  Ill,  p.  103,  1884. 
Nauta  Beck  (in  syn.),  Ind.  Moll.,  p.  166,  1838. 
Amplexa  Brown,  111.  Conch.  Gt.   Brit,  ed.  11,  p.   31,  1844  (err.  type);  not 

Amplexus  Brown,  op.  cit.,  p.  45. 
Aplecta  Herrmannsen,  Ind.   Gen.  Mai.,  I,  p.  65,  1846. — Fischer,  Manuel 

Conch.,  p.  511,  1883. 
Myxas  Gray,  Proc.  Zool.  Soc.  for  1847,  p.  180,  not  of  Leach,  1822. 
Bulinus  BiNNEY,  Land  and  Fw.  Sh.  N,  Am.,  li,  p.  97,  1865. —  Dall,  Ann. 

Lye.  N.  Hist.  N.  Y.,  ix,  p.  356,  1870. 
Nauta  Westerlund,  Fauna  Pal.  Reg.,  v,  p.  57,  1885. 

Shells  of  species  allied  to  Physa.,  but  usually  more  slender  and 
elevated,  the  mantle  not  extending  beyond  the  margin  of  the  aperture 
and  its  edge  entire,  without  filamentary  appendages ;    jaw  strongly 


FAMILY    PHYSID^  IO5 

arcuated,  thin,  cartilaginous,  without  accessory  plates ;  other  charac- 
ters as  in  Physa. 
Type  Bulla  hypnorum  Linn^,  1758,  Holarctic. 

The  nomenclature  of  this  genus  has  been  subject  to  some  vicissi- 
tudes. In  1757  Adanson,  who  did  not  adopt  the  binomial  nomencla- 
ture, described  a  minute  shell  from  the  fresh  waters  of  Senegal  under 
the  name  of  "  le  Bulin,  Bulinus"  From  its  form  and  size  it  was 
certainly  not  an  Aplexa^  but  rather  a  species  of  the  group  called  by 
Ehrenberg,  in  1831,  Isidora.  This  genus  has  the  jaw  and  radula  of  a 
Planorbis  and  may  be  regarded  as  a  physiform  relation  of  the  latter 
genus.  To  a  considerable  extent  it  replaces  Physa  in  tropical 
Africa. 

Scopoli  in  1777  attempted  to  utilize  Adanson's  researches,  and 
proposed  a  genus  Bulimus  in  which  he  included  Ltmncea^  Succinea 
and  Bythinia  (sp.),  attributing  the  genus  to  Adanson  and  paraphras- 
ing Adanson's  diagnosis  of  the  characters  of  the  animal.  The  name 
was  later  used  for  the  large  land  shells  for  which  it  is  familiar,  but  to 
which  the  diagnosis  cannot  be  applied. 

It  seems  almost  certain  that  Bulimus  (Scopoli)  is  a  misprint  for 
Bulinus  (Adanson),  but,  as  usual,  several  authors  have  not  hesitated 
to  propose  a  bogus  derivation  for  a  name  for  which  the  author  gave 
no  derivation,  and  have  ignored  the  statement  of  Adanson,  who  gives 
a  legitimate  and  totally  different  source  for  the  name. 

However  this  may  be,  Bulimus  long  had  currency  in  concho- 
logical  nomenclature  for  animals  with  which  we  are  not  here  con- 
cerned, and  in  1781  Otho  Friedrich  Miiller  revived  Adanson's  name 
in  its  original  form  for  the  group  named  Physa  by  Draparnaud 
twenty  years  later.  Miiller  included  in  his  list  of  species  Adanson's 
type  (to  which  he  gave  the  binomial  name  Bulinus  senegalensis^  ^ 
Bulinus  turritus  (=  Aplexa  hypnorum.  L.  sp.)  and  Bulinus  perla 
(=  Physa  fontinalis  Drap.). 

Since  he  states  that  his  genus  is  that  of  Adanson,  it  follows  that 
Adanson's  sole  species  must  be  taken  as  the  type,  which  eliminates  one 
of  the  three  groups  concerned.  For  the  group  represented  by  Physa 
fontinalis  Draparnaud's  name  has  been  generally  and  properly 
retained,  while  the  first  available  name  for  the  third  group  is  Aplexa 
Fleming.  This  is  accepted  and  defined  by  Sowerby  as  indicated  in  the 
synonymy  above  given,  but  may  have  been  used  earlier  in  print  by 
Fleming;  though  I  have  found  no  record  of  it  if  this  be  the  case. 
Sowerby  speaks  of  it  as  if  it  were  not  a  manuscript  name,  but  does  not 
explicitly  so  state. 


I06  LAND    AND    FRESH    WATER    MOLLUSKS 

Later  on  Herrmannsen  supplies  a  gratuitous  derivation  for  Fleming's 
name  and,  because  it  does  not  properly  conform  to  his  imaginary 
source,  alters  the  spelling  to  Aplecta. 

This  was  totally  unauthorized.  Since  no  derivation  w^as  given  by 
Sov^erby,  we  are  at  liberty  to  regard  the  word  as  an  arbitrary  combi- 
nation of  letters  formed  on  the  analogy  of  triplex  and  similar  Latin 
words,  but  we  are  not  at  liberty  to  manufacture  an  imaginary  deriva- 
tion and  then  force  the  name  to  conform  to  it. 

Several  authors  divided  Miiller's  group  differently,  and  several  syn- 
onyms were  proposed  for  parts  of  it,  as  will  be  evident  on  a  study  of 
the  synonymy. 

The  genus  occurs  in  the  Tertiary  of  Europe  and  North  America, 
and  possibly  as  far  back  as  the  Middle  Cretaceous  of  North  America. 
Several  well  characterized  forms  have  been  described  from  the  Lara- 
mie. The  type  is  known  from  the  Palearctic  and  Nearctic  regions, 
and  the  genus  extends  south  to  Mexico,  where  in  the  tropical  condi- 
tions of  Mazatlan  perhaps  the  finest  of  the  recent  species  occurs  abun- 
dantly. In  Alaska  and  on  the  adjacent  continent  of  Asia  but  one 
species  is  known,  the  type. 

Aplexa  hypnorum  (Linn6). 

Bulla  hypnorum  Linne,  Fauna  Suecica,  ed.  i,  No.  1303,  1746;  ed.   il,  No. 

2159,  P-  522,  1761  ;  Syst.  Nat  ,  ed.   x,  p.  727,    1758  ;  ed.  xii,  p.  1185, 

1767. 
Bulimus  hypnorum  Bruguie:re,  Encycl.  M^th.,  p.  301,  1792, 
Planorbis  turritus  Muller,  Verm.  Terr.,  11,  p.  169,  1774. 
Physa  hypnorum  Draparnaud,   Hist.,  p.   55,  pi.  iii,   figs.    12-13,  1805.  — 

Haldeman,  Mon.  Limn.,  p.  36,  pi.  v,  figs.  4-9,  1842.  —  Forbes  and 

Hanley,  Brit.  Moll.,  iv,  p.  143,  pi.  cxxii,  figs.  6-7. 
Bulla  hypnorum  Montagu,  Test.  Brit,  11,  p.  228,  1803. 
Bulla  turrita  Gmelin,  Syst.  Nat.,  vi,  p.  3428,  No.  20,  1792. 
Aplexa  hypnorum  Sowerby,  Genera,  fasc.  vii,  1822. —  Fleming,  Hist.  Brit. 

An.,  p.  276,  1828  ;  Encycl.  Brit.,  ed.  vii,  1837  ;  Art.  MoUusca,  reprinted 

as  •  Molluscous  Animals, '  8°,  Edinburgh,  p.  158,  1837. 
Turbo  stagnalisV^Ai.KTS.Yt.,  Test.  Min.  Rar.,  p.  15,  pi.  11,  fig.  54,  1787. 
Nauta  hypnorum  (Leach,  in)  Turton,  Man.,  p.  129,  1831. — Leach,  Syn. 

Moll.  Gt.  Brit.,  p.  no,  1852. 
Physa  hypnorum,  Hist,  des  Moll.,  p.  55,  pi.  lii,  figs.  12,  13,  1805. — Pfeiffer, 

Naturg.  Deutscher  Land.  Moll.,  i,  p.  97,  1821. 
Bullinus  turriius  OviK^,  Lehrb.  d.  Naturg.,  p.  303,  181 5. 
Physa  hypnorum  Lamarck,  Anim.  s.  Vert.,  vi,  Pt.  11,  p.  157,  1822. 
Physa  elongata  Say,  Journ.  Acad.  Nat.  Sci.  Phila.,  il,  p.  171,  182 1.  —Gould, 

Inv.  Mass.,  p.  214,  fig.  143,  1841.  — De  Kay,  Zool.  N.  Y.  Moll.,  p.  81, 

pi.  VI,  fig.  346,  1843. 
Physa  turrita  J.  de  C.  Sowerby,  in  Richardson,  Fauna  Bor.  Am.,  in,  p.  315, 

1836. 
Physa  glabra  De  Kay,  Zool.  N.  Y.,  Moll.,  p.  80,  pi.  v,  fig.  83,  1843. 


FAMILY    PHYSID^  I07 

Physa  elongatina  Lewis,  Proc.  Boston  Soc.  N.  Hist.,  v,  pp.  122,  298,  1855. 
Apiexus  hypnorum  Chenu,  Man.  de  Conch.,  i,  p.  481,  fig.  3556,  1859. 
Bulinus  hypnorutn  Binney,  Land  and  Fw.  Sh.  N.  Am.,  11,   p.  99,  fig.  170, 

1865. 
Bulinus  hypnorum  var.  picta  Krause,   Sitzb.  Ges.    Naturf.   Fr.  zu  Berlin, 

1883,  p.  32. — Martens,  Conch.  Mitth.,  11,  p.  184,  1885. 
Physa  hypnorum  var.  polaris  Westerlund,  Sib.  1.  u.  Sottv.   Moll.,  p.   56, 

1877. — Martens,  Conch.  Mitth.,  11,  p.  184,  1885. 
Physa  {Nauta)  hypnorum  lA^at. — Westerlund,  Fauna  Palaarct.,  Reg,  v,  p. 

57.  1885. 
Physa  {Nautd)  hypnorum  var.  polaris  Westerlund,  op.  cit,  p.  58. 

Range.  —  Northern  Europe,  Asia  and  America,  Northern  United 
States  and  Canada. 

English  River,  Manitoba.    Red  Deer,  McLeod,  Olds,  etc.,  in  Alberta. 
Great  Slave  Lake,  at  Fort  Resolution  !  York  Factory,  Hudson  Bay ! 

Yukon  River,  at  old  Fort  Yukon !  and  Nulato ! 
Alaska  ;  Porcupine  River  in  Alaska  !  also  Fort  Clar- 
ence !  and  the  Nushagak  River. 

Snake  River,  Idaho  !  Middle  Park,  Colorado  !  Up- 
per Missouri  in  Montana !  Utah  (Hemphill)  ! 

This  well  known  species  is  supposed  to  be  circum- 
boreal,  but  there  are  some  peculiarities  in  its  known  y\g  81.  A*- 
distribution.  While  it  extends  to  northern  and  west-  Uxa  hypnorum. 
ern  Alaska  and  down  into  the  mountainous  region  in 
Colorado  and  Utah,  it  has  not  been  reported  so  far,  authentically,  from 
west  of  the  Cascades,  either  in  the  United  States  or  British  Columbia. 
There  was  one  record  "  near  Puget  Sound  "  by  Dr.  J.  G.  Cooper,  which 
is  cited  by  W.  Cooper  and  Carpenter,  but  this  refers  to  a  shell  obtained 
at  Vancouver,  Wash,  (not  Vancouver  Island) ,  by  Sir  George  Simp- 
son, which  was  afterward  described  by  Dr.  Lea  as  Physa  hordeacea. 
It  is  not  positively  known  that  this  species  is  not  a  Physa.,  though 
Tryon  has  referred  it  to  Bulinus  (=  Aplexd).,  on  the  strength  of  its 
general  aspect. 

A  number  of  varieties  have  been  proposed,  but  there  is  not  much 
systematic  basis  for  such  of  these  mutations  as  I  have  seen. 

Genus  Ancylus  Miiller. 

Subgenus  Ancylus  s.  s. 

Patella  (sp.)  Linn6,  Syst.  Nat.,  ed.  x,  p.  783,  1758. 

Ancylus  Geoffroy,  Traite  som.  des  Coq.  Fluv.  Paris,  pp.  122,  124,  1767;  not 

binomial,  sole  example  Patella  lacustris  Linn6.   Ibidem,  translation  by 

Martini,  pp.  108,  no,  1767. 
Ancylus  O.    F.    Muller,   Hist.   Verm.,    11,  p.    199,    1774,   A.  lacustris  and 

fluviatilis  Muller;  Zool.    Dan.    Prodr.,    p.    237,    1776.  —  Draparnaud, 

Tabl.,  pp.  30,  46,  1 801  ;  Hist,   des  Moll.  Terr,  et  Fluv.  de  France,  pp. 


I08  LAND    AND    FRESH    WATER    MOLLUSKS 

25,  28,  47,  1805.  — RoissY,  Moll.,  V,  p.  223,  1805. — BowDiCH,  Elem. 
Conch.,  I,  pp.  24,  63,  1822  ;  A.  fluviatilis  selected  as  type.  —  Nilsson, 
Hist.  Moll.  Svecias,  p.  83,  1822.  —  Lamarck,  Hist.  An.  s.  Vert.,  vi,  2, 
p.  25,  1822. — Beck,  Ind.  Moll.,  p.  123,  1837  ;  A.  fluviatilis  L.,  ist  sp. 
—  Haldeman,  Mon.  Limn.,  p.  14,  1842, 

Ancyclus  Say,  Nicholson's  Encycl.,  3d  ed.,  11,  p.  14,  1819. 

Ancylastrum  (s^.)BovKGViG^ AT,  P.  Z.  S.,  1853,  p.  79,  July,  1854. — Clessin, 
Conch.  Cab.,  ed.  11,  p.  10,  1880;  A.  fluviatilis  selected  as  type. — 
Fischer,  Man.  Conchyl.,  p.  504,  1883. — Tryon,  Struct,  and  Syst. 
Conch.,  Ill,  p.  107,  1884  ;  noX  Ancy lustrum  Bourg.,  1853,  typical. 

Ansulus  sive  Ansylus  Gray,  in  Turton,  Man.,  p.  247,  1840.  —  Herrmann- 
sen,  Ind.  Gen.  Mai.,  i,  p.  52,  note  13,  1846. 

Ancyllus  Graells,  Cat.  Moll.  Espana,  p.  22,  1846  ;  err.  typ.  ? 

'^  Haldemania  Clessin,  1880,  not  of  Tryon,  1862. 

Subgenus  Acroloxus  Beck. 

Acroloxus  Beck,  Ind.  Moll.,  p.  124,  1837,  ist  sp.  A.  radiatus  Guilding,  1828, 
not  of  Orbigny,  1825  ;  also  includes  A.  lacttstris  (\^.)  Miiller  ;  Herrmann- 
sen,  Ind.  Gen.  Mai.,  i,  p.  16,  1846,  selects  A.  lacustris  as  type. — W. 
G.  Binney,  Land  and  Fw.  Sh.  N.  Am.,  11,  p.  147,  1865. 

Acroxus  BouRGUiGNAT,  J.  de  Conchyl.,  iv,  p.  169,  1853;  a  modification  of 
Acroloxus  Beck. 

Velletia  Gray,  in  Turton,  Man.,  pp.  66,  230,  250,  1840  ;  sole  ex.  A.  lacustris 
Miiller.  —  Haldeman,  Mon.  Limn.,  p.  14,  1842.  —  Gray,  P.  Z.  S., 
1847,  p.  181  ;  A.  lacustris.  — Bourguignat,  J.  de  Conchyl.,  iv,  p.  63, 
1853  ;  P.  Z.  S.,  1853,  p.  79,  July,  1854.  — Fischer,  Man.,  p.  504,  1883. 

Subgenus  Ancylastrum  Bourguignat. 

Ancylastrum  Bourguignat,  Journ.  de  Conchyl,  iv,  pp.  63,  170,  1853  (Feb.), 
A.  cumingianus  Bourguignat  (Tasmania)  selected  as  type  ;  P.  Z.  S., 
1853,  p.  91  (not  p.  80),  1854. —  Hedley,  Proc.  Mai.  Soc,  i,  p.  118,  1894. 
Not  Ancylastrum  Clessin,  1880,  and  Westerlund,  1902. 

Cumingia  Clessin,  Conch.  Cab.,  ed.  11,  pt.  299,  Mon.  Ancylus,  p.  10,  1880; 
type  yi.  cumingianus  Bourg. —  Tryon,  Struct.  Syst.  Conch.,  iii,  p.  107, 
1884.     Not  Cumingia  Sowerby,  P.  Z.  S.,  1833,  p.  34. 

Legrandia  Hanley,  Proc.  Roy.  Soc.  Tasmania  for  1871,  p.  27,  1872.  Type 
A.  cumingianus  Bourg. 

?  Subgenus  Gundlachia  Pfeiffer. 

Gunai.achia  Pfeiffer,  Zeitschr.  fiir  Mai.   for  1849,   P-   97<    i^S^ ;  type  G. 

ancyliformis  Pfeiffer,  Cuba  ;  cf.  Nordenskiold,  Zool.  Anz.,  xxvi,  pp.  590- 

593,  July,  1903;  and  Dall,  Nautilus,  xvii,  Jan.,   1904,  pp.  97-8,  1904; 

also  J.  G.  Cooper,  Proc.  Cal.  Acad.  Sci.,  vi,  p.  26,  1875. 
Poeyia  Bourguignat,  Spicil.  Mai.,  xciv,  Jan.,   1862,  Rev.  de  Zool.,  p.  13, 

1862.     Sole  ex.   P.  gundlac hioides  ViOMx^.,  =■  Gundlachia  test.  juv.  fide 

Fischer. 

The  genus  Ancylus  cannot  be  cited  as  of  Geoffroy,  first,  because 
that  author  did  not  adopt  the  Linnean  nomenclature,  and  secondly, 
because  his  only  species  was  identified  by  him  with  Patella  lacustris 
L.,  which  is  the  type  of  Acroloxus^  and,  though  Bourguignat  and 


FAMILY    PHYSID^  IO9 

Others  have  tried  to  propagate  the  view  that  Geoffroy's  species  was  the 
A.  Jluviatilis ^  their  arguments  cannot  be  said  to  outweigh  the  positive 
statement  of  the  original  author.  The  first  binomial  author  to  use 
Ancylus  was  Miiller,  who  must  be  credited  with  the  genus.  The  name 
Ancylastrum^  published  by  Bourguignat  (though  probably  suggested 
by  Moquin  Tandon)  was  doubtless  intended  to  be  the  equivalent  of 
Ancylus  s.  s.,  but  the  publishing  author  distinctly  and  repeatedly 
announced  the  type  to  be  Ancylus  cumingianus ^  which  differs  in 
many  respects  from  typical  Ancylus^  and  will  therefore  retain  the  name, 
which  otherwise  would  have  fallen  into  the  synonymy  of  Ancylus  s.  s. 
Acroloxus  Beck,  typified  by  A.  lacustris  Miiller,  seems  to  be  a  well 
characterized  subdivision.  Beck's  first  species  was  examined  by  Gray 
and  determined  to  be  a  Velletia^  which  is  an  exact  synonym  of  Acro- 
loxus. Protancylus  was  proposed  by  the  Sarasin  brothers  in  1898, 
for  a  form  resembling  Ancylus^  from  Celebes,  but  in  which  the  gill  is 
fully  developed. 

Typical  Ancylus  seems  to  be  an  Old  World  form,  but  Acroloxus  is 
represented  in  both  hemispheres.     The  subdivisions  of  the  typical  sub- 
genus so  far  recognized  are  as  follows  : 
?  Brondelia  Bourguignat,  Rev.  de  Zool,  p.  13,   1862;  Spic.  Mai., 

xcv,  Jan.,  1862,  type  B.  drouetiana  Bourg.,  Algeria. 

This  form,  which  is  said  to  be  an  air-breather,  a  fact  needing  con- 
firmation, is  radiately  ribbed  and  has  a  sinistral  apex.     More  informa- 
tion about  it  is  much  needed,  and  it  may  prove  to  be  an  Acroloxus . 
Lanx  Clessin,  Conch.  Cab.,  ed.  11,  pt.  299,  p.  10,  1880;  type  A.  new- 

berryi  Lea,  Oregon  and  California. 

The  type  has  a  smooth  or  concentrically  striated  apex,  subcentrally 
situated,  obtuse  ;  the  shell  is  larger  and  more  solid  than  the  majority 
of  the  genus.  A.  patelloides  Lea,  placed  by  Clessin  with  the  above, 
has  a  shell  like  A.  newberryi,  but  more  delicate,  depressed,  and  with 
a  well  marked  radial  system  of  coloration. 

The  following  groups  are  Nearctic  or  American ;  Ferrissia  is  also 
South  African. 
Lcevapex  Walker,  Nautilus,  xvii,  June,  1903,  p.  15 ;  type  Ancylus 

fuscus  C.  B.  Adams.    Chiefly  lacustrine,  with  a  smooth  nepionic 

shell. 
Ferrissia  Walker,  op.  cit.,  p.    15;    type  Ancylus    riimlaris    Say. 

Chiefly  fluviatile,  with  a  radiately  sculptured  nepionic  shell. 

The  question  as  to  whether  Gundlachia  is  a  distinct  genus  or  merely 
an  exceptional  second-season  growth  of  Ancylus^  has  been  discussed 


no  LAND    AND    FRESH   WATER    MOLLUSKS 

by  me  in  the  paper  cited  in  the  synonymy,  since  publishing  which  I 
find  Dr.  J.  G.  Cooper  had  also  expressed  the  same  opinion  in  1875. 

Ancylus  (Ferrissia)  rivularis  Say. 

Ancylus  rivularis  Say,  Journ.  Acad,  Nat.  Sci.,  i,  p.  124,  1817. —  Haldeman, 
Mon.  Limn.,  p.  4,  pi.  i,  fig.  i,  1844  (Delaware  River). 

Ancyclus  rivularis  Say,  Nicholson's  Encyclopedia,  3d  ed.,  Art.  Conchology, 
vol.  II,  p.  14,  1819. 

Ancylus  {Ferrissia)  rivularis  Bryant  Walker,  The  Nautilus,  xvii,  No.  2,  p. 
15,  June,  1903  ;  xviii.  No.  2,  p.  17,  pi.  i,  figs,  i-io,  13-15,  June,  1904. 

Range. — Northern  United   States  east   of   the  Mississippi,  New 
Mexico,  Canada,  Manitoba. 

Souris  River,  Manitoba,  Dawson. 

Ancylus  (Ferrissia)  parallelus  Haldeman. 

Ancylus parallelus  Haldeman,  Mon.  Limn.,  pt.  2,  p.  3  of  cover,  1841  (Ver- 
mont) ;  pt.  7,  p.  II,  pi.  I,  fig.  6,  1844. —  BiNNEY,  Land  and  Fw.  Sh. 
N.  Am.,  II,  p.  142,  1865. 

Range.  —  New  England ;  Canada,  Manitoba. 

Pine  Creek ;  Rainy  River ;  and  Lake  of  the  Woods,  in  Manitoba. 

Ancylus  (Laevapex)  fragilis  Try  on. 

Ancylus  fragilis  Tryon,  Proc.  Acad.  Nat.  Sci.  Phila.,  for  1863,  p.  149,  pi.  i, 
fig.  15. —  Binney,  Land  and  Fw.  Sh.  N.  Am.,  11,  p.  146,  fig.  246  (Cali- 
fornia), 1865.— Tryon,  Mon.  Fw.  Univ.  Moll.  U.  S.,  p.  229,  pi.  2,  figs.  17, 
18,  1872. 

? Ancylus caurinus  Cooper,  Rep.  N.  Hist.  Wash.,  p.  378,  1859  ;  Pacific  R.  R. 
Reps,,  XII,  p.  378,  1859,  nude  name. — Binney,  Land  and  Fw.  Sh.  N. 
Am.,  II,  p,  144,  fig.  243,  1865  ;  Proc,  CaL  Acad.  Sci,,  iv,  p.  100,  1870. 
Black  River,  Puget  Sound, 

Range. — California  ;  Puget  Sound  drainage 
{caurinus)^  Vancouver  Island  near  Victoria ! 
(^caurinus^ . 

Tryon   unites   these   under  his    prior  name. 

The  Vancouver  specimens  are  certainly  iden- 
FiG.  82.    Ancylus  koo-      .     ,       .  ,    ^  ,      ,    „ 

taniensis  Baird.  ^ical  with  Cooper  s  shell. 

Ancylus  (Laevapex)  kootaniensis  Baird. 

Ancylus  kootaniensis  Baird,  Proc,  Zool,  Soc,  London,  for  1863,  p,  69, — 
Binney,  Land  and  Fw.  Sh,  N.  Am.,  11,  p.  144,  fig,  242,  1865,  — Tryon, 
Mon.  Fw,  Univ,  Moll,  U.  S,,  p,  227,  pi,  11,  figs,  11-12,  1872, 

Range.  —  Kootenai  and  Spokane  Rivers,  British  Columbia. 


FAMILY    SIPHONARIID^  III 


Family  SIPHONARIIDiE. 
Genus  Siphonaria  Sowerby. 

Siphonaria  Sowerby,  Genera  of  Shells,  pt.  xxi,  Jan.,  1824  ;  Proc.  Zool.  Soc. 
London,  for  1835,  p.  6. —  Dall,  Am.  Journ.  Conch.,  vi,  p.  31,  1870. 

Muretia  D'Orbigny,  Voy.  Am.  Merid.,  p.  682,  1846.  Not  Mouretia  Sow- 
erby, 1835. 

Trimusculus  (Schmidt,  MS.)  Moller,  Isis,  1832,  p.  132. 

f  Liria  Gray,  Phil.  Mag.  and  Journ.,  lxiii,  p.   275,  April,  1824. 

The  type  of  Liria  is  Le  ZeVz' Adanson,  Senegal,  p.  32,  pi.  2,  fig. 
2,  1757  j  stated  by  Gray  to  be  a  synonym  of  Sowerby's  genus,  but  it  is 
probable  that  Adanson's  shell  is  not  a  Siphonaria. 

Subgenus  Siphonaria  s.  s. 
Siphonaria  Dall,  Am.  Journ.  Conch.,  vi,  p.  31,  1870. 

Shell  solid,  porcellanous,  with  subcentral  apex  and  radial  sculpture  ; 
inner  lateral  teeth  of  the  radula  bifid,  outer  trifid.  Habitat,  tropical 
or  warmer  seas.     Type,  S.  sipho  Sowerby. 

Subgenus  Liriola  Dall. 
Liriola  Dall,  Am.  Journ.  Conch.,  vi,  p.  32,  1870. 

Shell  thin,  homy,  with  apex  eccentric ;  smooth  or  faintly  radially 
striate.  Habitat,  cooler  or  temperate  seas.  Type  S.  thersites  Car- 
penter. 

Siphonaria  (Liriola)  thersites  Carpenter. 

Siphonaria  thersites  Carpenter,  Ann.  Mag.  N.  Hist.  (3),  xiv,  p.  425,  Dec, 

1864.     Neah  Bay,  Wash. 
Siphonaria  {^Liriola)  thersites  Dall,  Am.  Journ.  Conch.,  vi,  pp.   32,  33,  pi. 

IV,  fig.  8,  pi.  V,  figs.  2,  5,  1870. 

Range.  —  Strait  of  Fuca  to  the  Aleutian  Islands,  on  stones  near 
low  water  mark. 

Neah  Bay,  Wash.  !  Victoria,  British  Columbia ;  Fort  Simpson, 
British  Columbia ;  in  Alaska  at  Port  Mulgrave !  Port  Etches  !  St. 
Paul,  Kadiak !  Chirikof  Island !  Semidi  Islands !  Simeonof  Island 
and  Popof  Strait,  Shumagin  Islands  !  Chika  Islands,  Unalga  Pass  ! 
Captains  Harbor,  Unalaska  !  Constantine  Harbor,  Amchitka !  Kiska 
Harbor,  Kiska  Island,  Aleutians. 

This  is  one  of  the  most  common  and  characteristic  mollusks  of  the 
northwest  coast.  It  lives  between  tidemarks,  often  where  it  must  be 
submerged  twenty  out  of  twenty -four  hours  of  the  day,  but  is  some- 
times dredged  in  20  fathoms,  dead. 


112  LAND    AND    FRESH    WATER    MOLLUSKS 

Family  ONCHIDIIDJE. 
Genus  Onchidium  Buchanan,  1800. 
Type  Onchidium  typkce  Buchanan,  Trans.  Linn.  Soc,  V,  p.   132, 

1800. 

Subgenus  Onchidella  Gray,  1850. 

Type  Onchidium  nigricans  Quoy,  Fig.  Moll.  An.,  iv,  p.  ii7»  pl« 
181,  fig.  I,  1850  (selected  as  type  by  Herrmannsen,  Ind.  Gen.  Mai., 
Suppl.,  1852). 

Dorsal  surface  without  arborescent  processes,  margin  of  the  mantle 
with  prominent  spaced  papillae,  serving  as  conduits  for  mucous  glands  ; 
lower  surface  of  the  mantle  with  muciparous  glands ;  dorsum  with 
dorsal  eyes  ;  mouth  agnathous.     Warmer  seas. 

Section  Arctonchis  Dall,  nov. 

Species  small,  like  Onchidella^  but  without  muciparous  glands  on 
the  lower  side  of  the  mantle,  without  dorsal  eyes  and  with  a  jaw; 
Cool  temperate  and  boreal  coasts. 

Type  Onchidella  borealis  Dall. 

I  had  long  since  proposed  to  retain  for  this  group  the  name  Onchi- 
della^ supposing  that  name  to  be  practically  a  synonym  of  Onchidium. 
This,  however,  is  not  now  regarded  as  allowable,  and  Onchidella  must 
follow  the  fate  of  its  type. 

I  propose  therefore  the  sectional  name  Arctonchis  for  the  group  of 
small  boreal  Onchidella  which  includes  at  least  O.  borealis  and 
O.  celtica  Forbes  and  Hanley. 

Onchidella  (Arctonchis)  borealis  Dall. 

Onchidella  borealis  Dall,  Am.  Journ.  Conch.,  vii,  p.  135,  1871.  —  W.  G. 
BiNNEY,  Proc.  Acad.  Nat.  Sci.  Phila.,  1876,  p.  84,  pi.  vi,  figs,  e,  ee, 
Sept.,  1876.  —  Binney,  Terr.  Airbr.  Moll.  U.  S.,  Third  supple..  Bull. 
Mus.  Comp.  Zool.,  xix.  No.  4,  pi.  vi,  figs,  d,  e,  1890  (called  carpenteri 
by  error,  in  text  pp.  214,  224)  ;  Fourth  Supplement,  Bull.  Mus.  Comp. 
Zool.,  XXII,  No.  4,  p.  202,  1892. 

Onchidium  boreale  Dall,  Semper,  Arch.  Phil.  Bd.  3,  heft  vi,  p.  282,  pi. 
XXI,  fig.  13. 

Range.  —  California  to  Bering  Sea  on  the  N.  W.  coast  of  America. 

California  (Binney)  ;  Coos  Bay,  Oregon  (Hemphill)  ;  Victoria, 
Vancouver  Island  !  Lituya  Bay  !  Port  Mulgrave  !  Port  Etches  !  Una- 
laska  !  and  Port  MoUer  on  Bering  Sea  !  in  Alaska. 

Observations  on  this  species  have  been  published  by  the  writer,  Mr. 
W.  G.  Binney,  Semper,  and  Henry  Hemphill ;  and,  as  their  articles 
are  short  and  widely  scattered  in  the  literature,  an  abstract  of  the 


FAMILY   ONCHIDIID^  II3 

whole,  with  additions,  is  now  given  so  that  the  data  in  regard  to  this 
species  may  be  obtained  in  one  place. 

The  animal  lives  between  tides,  where  at  high  water  it  is  covered 
by  the  sea,  usually  on  stones  or  projecting  rocks,  either  where  it  is  cov- 
ered with  Fucus  or  on  the  underside  of  stones  which  thus  form  a 
shelter.  It  seems  to  be  gregarious  in  its  habits,  as  many  as  fifty  speci- 
mens having  been  taken  from  a  single  crevice  in  shaly  rock.  When  in 
motion  it  moves  quite  rapidly  for  so  small  an  animal,  with  two  short 
stout  tentacles  tipped  by  keen  black  eyes  protruding  beyond  the  front 
edge  of  the  mantle.  The  upper  surface  is  dark  slate  color,  with  spots 
or  streaks  of  light  gray  or  whitish.  It  appears  smooth,  but  as  if  hav- 
ing small  round  tubercles  beneath  the  smooth  skin,  which  when  the 
animal  is  contracted  in  alcohol  are  much  more  conspicuous  than  in  life. 
Around  the  edge  of  the  mantle  is  a  single  row  of  larger  and  more 
prominent  tubercles  corresponding  to  an  equal  number  of  mucous  glands. 
These,  projecting,  give  the  margin  a  serrate  or  fringed  appearance. 
The  animal,  when  in  motion,  is  about  twelve  millimeters  long,  four 
and  one  half  wide,  and  three  millimeters  high,  oblong  oval  in  form,  a 
little  wider  behind  than  in  front.  When  at  rest  in  a  contracted  state 
it  is  nearly  circular  in  form,  a  little  longer  than  wide,  the  center  of 
the  dorsum  elevated  in  a  bluntly  pointed  manner,  giving  the  creature 
much  the  aspect  of  a  young  Acmcea.  The  lower  surface  of  the  body 
is  of  a  greenish  white,  and,  when  the  animal  is  moving,  the  foot 
seems  to  undergo  rapid  undulation.  The  muzzle  exhibits  anterior 
ovate  extensions  separated  by  a  sulcus  in  the  median  line,  as  in  other 
species  of  the  genus. 

Neither  Onchidella  borealis  nor  O.  celtica  possesses  the  singular 
dorsal  eyes  characteristic  of  many  tropical  species. 

O.  borealis  differs  from  O.  carpenteri  Binney,  and  all  the  other 
species  of  the  family  now  known  (except  O.  celticum) ,  in  possessing 
a  thin  delicate  smooth  jaw,  the  presence  of  which  has  been  demon- 
strated by  both  Binney  and  Semper.  According  to  Joyeaux  Laffluie 
O.  celticum  also  possesses  a  jaw,  though  the  surface  of  the  dorsum  is, 
if  the  figure  given  by  Forbes  and  Hanley  be  accurate,  much  more 
prominently  tuberculous  than  in  O.  borealis.  O.  carpenteri  Bin- 
ney, a  small  species  reported  by  Binney  from  California  and  Puget 
Sound,  is  according  to  that  author  agnathous,  and  therefore  belongs  to 
the  typical  section  of  the  genus. 

The  dentition  of  O.  borealis  has  been  worked  out  by  Binney  and 
confirmed  by  Semper.  The  radula  is  long  and  wide,  the  teeth  arranged 
strongly  en  chevron^  with  a  formula  of  -jr  *  ^  *  ^'     ^^^  rhachidian 


114  LAND    AND    FRESH    WATER    MOLLUSKS 

tooth  is  large,  longer  than  wide,  truncated  above,  expanded  below  its 
middle,  and  incurved  at  the  basal  margin.  The  reflected  portion  is 
large,  tricuspid,  the  cusps  prominent.  The  laterals  have  a  long,  nar- 
row base  of  attachment,  a  small  portion  of  its  upper  part  thrown  out- 
ward, the  rest  curving  inward,  giving  an  irregular  arcuate  form  to  the 
base  as  a  whole ;  the  anterior  and  posterior  margins  of  this  base  are 
abruptly  truncate.  The  reflected  part  is  rather  posterior  and  carries  a 
large,  wide,  expanding,  bluntly  truncated  cusp  on  the  outer  side,  and 
on  the  inner  a  very  small  conical  cusp.  The  successive  teeth  laterally 
from  the  middle  of  the  radula  at  first  increase,  then  gradually  decrease 
in  size,  but  retain  essentially  the  same  characters  to  the  outer  termina- 
tion of  the  row. 

From  the  typical  Onchidium  {schrammt  Bland  and  Binney, 
Guadeloupe,  W.  I.)  the  teeth  differ  by  the  wider  rhachidian,  with 
more  nearly  equal  cusps,  by  the  presence  of  two  distinct  cusps  on  the 
laterals,  and  by  the  curve  of  the  lateral  bases,  which  in  O.  schrammi 
have  their  posterior  portions  curved  toward  the  center  of  the  radula, 
while  in  O.  borealis  the  curve  is  in  the  opposite  direction.  In  Onchi- 
della  Jloridana  Dall,  an  oculiferous  agnathous  species  from  Knight's 
Key,  Florida,  the  discrepancy  of  the  rhachidian  cusps  and  the  curve 
of  the  lateral  bases  agree  with  O.  schrammi^  but  there  is  a  small 
accessory  inner  cusp  to  the  laterals. 

Mr.  Binney  informs  me  that  the  liver  in  O.  borealis  is  in  fasciculi 
of  long  casca,  one  on  each  side ;  there  is  also  an  accessory  lateral 
pouch  to  the  stomach,  which  also  has  a  fasciculus  of  caeca,  making 
three  biliary  ducts. 

According  to  Semper  this  species  agrees  in  most  respects  with  the 
fifth  of  the  groups  into  which  he  divides  Onchidium.  There  is  a 
single  row  of  large  glands  which  open  through  equally  spaced  small 
tubercles  on  the  mantle  edge.  The  other  glands,  which  in  the  other 
species  (except  O.  celtica)  empty  on  the  under  surface  of  the  mantle, 
are  absent  in  this  form.  The  penis  is  short  and  thick,  consisting  of 
two  well  marked  portions.  In  the  posterior  thinner  part  a  short 
broad  penial  papilla  is  present,  at  the  base  of  which  the  spermatic 
duct  opens.  The  wall  of  this  part  is  marked  by  extremely  shallow 
grooves  in  which  concretions  are  present,  very  like  those  found  in  the 
deep  grooves  of  other  species.  The  spermatic  cord  is  short  and  feebly 
twisted.  The  penial  retractor  muscle  is  thin  and  attached  proximally 
to  the  middle  of  the  pericardial  sac  on  the  inner  surface  of  the  foot. 
The  jaw  and  radula  are  as  described  by  Binney. 

I  should  like  here  to  record  my  dissent  from  the  ingenious  hypothesis 


FAMILY    AURICULID^  II5 

by  which  Semper  associated  the  occurrence  of  dorsal  eyes  in  Onchi- 
dium  with  the  presence  of  the  fish  Periopthalmus.  There  are  both 
oculiferous  and  (dorsally)  blind  species  of  Onchidium  in  the  Gala- 
pagos, and  an  oculiferous  species  in  Florida  and  Bermuda,  and  in 
neither  of  these  regions  is  Periopthalmus  known.  It  is  of  course  not 
only  necessary  that  an  hypothesis  should  account  for  the  facts,  but  that 
it  also  should  be  true,  but  the  latter  half  of  the  proposition  is  only  too 
liable  to  be  left  unverified. 

Family  AURICULID^. 
Genus  Carychium  Muller. 

Carychium  O.  F.  Muller,  Hist.  Verm.,  11,  p.  125,  1774  ;  sole  ex.  C.  mini- 
mum yLuWQx  \  Zool.  Dan.  Prodr.,  p.  xxix,  1776. —  Draparnaud,  Hist. 
Moll.  Terr.,  p.  57,  1805  (in  synonymy). 

Helix  (sp.)  Gmelin,  Syst.  Nat.,  vi,  p.  3665,  1792. 

Bulimus  (sp.)  Bruguiere,  Encyc.  Meth.,  i,  p.  310. 

Turbo  {s^.')  Montagu,  Test.  Brit.,  p.  339. 

Auricula  (sp.)  Draparnaud,  Tableau  des  Moll.,  p.  54,  1801  ;  Hist.,  p.  57, 
pi.  Ill,  figs.  18,  19,  1805. 

Odostomia  (sp.)  Fleming,  Edinb.  Encycl.,  vii,  p.  'jd,  181 7. 

y4«nV-(?//a(BRARDMS.)JURiNE,  Helvet.  Almanach,  p.  34,  1817. —  Hartmann, 
in  Steinmiiller,  Neue  Alpina,  i,  pp.  49,  205,  215,  1821  ;  and  Sturm, 
Fauna,  vi,  heft  v,  p.  36,  1821  ;  Syst.  Uebersetz.,  table,  1840. — 
MoQUiN  Tandon,  Hist.  Moll.  Terr.  Fr.,  11,  p.  413,  1855.  Type  C.  mini- 
mum Muller. 

Auriculina  Moquin  Tandon,  Hist.  Moll.  Terr.  Fr.,  11,  p.  646,  1855  ;  not  of 
Grateloup,  1838,  nor  Gray,  1847. 

Saraphia  (sp.)  Risso,  Hist.  Eur.  Men,  iv,  p.   84,  1826  ;  5*.  tridentata  Risso. 

<  Carychium  Leach,  Zool.  Misc.,  I,  p.  85,  1814. —  F^russac,  Prodr.,  p.  100, 
1819  ;  Tabl.  Syst.,  p.  xxxiii,  1821. — Blainville,  Diet.  Sci.  Nat.,  vii,  p. 
187. — MoQuiN  Tandon,  Hist.  Moll.  Terr.  Fr.,  pp.  412,  413,  1855. 


Fig.  83.     Carychium  exiguutn  Say.    Animal  and  shell  magnified. 

The  species  of  this  genus  are  so  small  that  a  special  search  almost 
is  necessary  to  determine  their  presence  or  absence  in  a  given  locality. 


Il6  LAND    AND    FRESH   WATER   MOLLUSKS 

So  it  is  uncertain  whether  the  range  herein  reported  might  not  be  con- 
siderably extended  if  thorough  collecting  had  been  done, 

Carychium  exiguum  Say. 

Pupa  exigua  Say,  Journ,  Acad.  Nat.  Sci.  Phila.,  ii,  p.  375,  1822. —  Gould, 
Boston  Journ.  Nat.  Hist.,  iii,  p.  398,  pi.  iii,  fig.  20,  1841. 

Carychium  exiguum  Pfeiffer,  Wiegman's  Archiv,  i,  p.  224,  1841. — BlN- 
NEY,  Land  and  Fw.  Sh.  N.  Am.,  11,  p.  6,  figs.  5-9,  1865. 

Range.  —  Temperate  North  America. 

At  Brandon,  Pine  Creek,  and  Carberry,  Manitoba ;  Salt  Spring 
Island,  and  at  Comox,  Vancouver  Island,  British  Columbia. 

Carychium  exile  Lea. 

Carychium  exile  H.  C.  Lea,  Am.  Journ.  Sci.,  ist  ser.,  xlii,  p.  109,  pi.  i, 
fig.  5,  1841.  —  Troschel,  Arch,  fur  Naturg.,  11,  p.  128,  1843.  Not  C. 
exile  C.  B.  Adams,  Contr.  Conch.,  iii,  p.  38,  1849  (Jamaica). 

Range.  —  Eastern  United  States.  Manitoba,  in  drift  of  the  Red 
River  of  the  North. 

In  the  description  of  the  animal  of  Carychium  cited  by  Binney 
(under  C.  exiguum)  and  copied  by  Baker  (Moll.  Chicago  Area,  11,  p. 
254)  the  w^riter  has  confused  the  anterior  end  of  the  wide  muzzle  with 
the  foot,  although,  by  the  figure  adjacent  to  this  paragraph,  the  rela- 
tion of  the  parts  is  clearly  shown.  The  foot  of  the  animal  is  not 
"  divided  into  two  segments,"  but  is  entire,  as  required  by  the  generic 
diagnosis. 

Family  STREPOMATID^. 

Genus  Pleurocera  Rafinesque. 

*  Pleurocera  canaliculata  Say. 

Melania  canaliculata  Say,  Journ.   Acad.  Nat.   Sci.   Phila.,   ll,  p.    175,  1821. 

Ohio. 
Melania  conica  Say,  op.  cit.,  p.  176,  1821.  — Sowerby,  in  Richardson,  Fauna 

Boreali  Am.,  in,  p.  316,  1836. 

Range-.  —  Ohio,  Tennessee  and  Alabama,  Indiana  and  Illinois. 

This  species  is  cited  in  J.  de  C.  Sowerby's  very  inaccurate  list,  as 

coming  from  "  Lake  Superior  to  the  Saskatchewan."     No  subsequent 

collector   has   confirmed  this  statement,  which  is  doubtless   entirely 

erroneous. 

Genus  Goniobasis  Lea. 

Goniobasis  plicifera  Lea,  var.  silicula  Gould. 

Melania  plicifera  Lea,  Trans.  Am.   Phil.  Soc,  vi,  p.  93,  pi.  xxill,  fig.  90, 

1836.    Oregon. 
Melania  silicula  GouLD,  Proc.  Bost.  Soc.  Nat.  Hist.,  11,  p.  224,  1847  ;  Wilkes' 

Exped.,  Moll.,  p.  141,  figs.  164,  164a,  1852.     Nisqually,  Oregon. 


FAMILY    AMNICOLID^  II7 

Range.  —  Northern  California,  Oregon  and  Washington. 

Vancouver  Island  (Forbes)  ?  British  Columbia  in  streams  west  of 
the  Cascades  (Lord). 

This  species  so  much  resembles  the  viviparous  Melania  of  the  Ha- 
waiian Islands  and  the  Orient,  wliich  has  a  fringed  mantle  edge,  that 
for  a  long  time  it  was  doubted  whether  the  little  group  of  Pacific 
Coast  species  was  not  related  to  the  oriental  forms  rather  than  to  the 
Goniobasis  of  the  eastern  United  States.  An  examination  of  the  liv- 
ing animal  by  the  writer  a  few  years  ago  showed,  however,  that  the 
Oregon  species  has  a  plain  mantle  edge  and  is  oviparous,  so  that  the 
resemblance  referred  to,  though  obvious,  is  probably  merely  the 
result  of  convergence,  and  expresses  no  intimate  relationship. 

Tryon  regarded  Gould's  silicula  as  a  species  ;  others  have  thought  it 
a  variety  of  the  older  plicif era.  Further  studies  are  necessary  to  de- 
termine the  question. 

Family  AMNICOLIDiE. 
Genus  Amnicola  Gould  and  Haldeman. 
Amnicola  limosa  Say. 

Paludina  limosa  Say,  Journ.  Acad.  Nat.  Sci.  Phila.,  i,  p.  125,  181 7. — 
Nicholson's  Encyc,  third  American  ed.,  p.  12,  1819. 

Paludina porata  Say,  journ.  Acad.  Nat.  Sci.  Phila.,  11,  p.  174,  1821. 

Amnicola porata  Gould,  Inv.  Mass.,  p.  229,  fig.  157,  1841. 

Amnicola  limosa  Haldeman,   Men.   Limn.,  p.  10,  pi.  i,  figs.  5,  6,    1845.  — 
BiNNEY,  Land  and  Fw.  Sh.  N.  Am.,  iii,  p.  84,  fig.  166, 
1865.  A 

Lyogyrus  lehnerti  Ancey  (Monstr.).  V  V^ 

Range.  —  Virginia  to  Wisconsin  and  Hudson  Bay.  ^^ 

Lake  Superior  to  the  Height  of  Land ;  Athabaska       /)°',^*   '^"'' 
at   Lake   La   Loche    (Richardson) ,  N.  Lat.  56°  30' ; 
Lake  of  the  Woods ;  Manitoba ;  Moose   Factory,  Hudson  Bay !  Big 
Sioux  River,  Nebraska  !  Salt  Lake  basin,  Utah  Lake  !  Utah. 

This  is  the  type  of  the  genus,  and  it  seems  to  reach 
Ak  the  headwaters  of  the  Atlantic  and  Hudson  Bay  drain- 

nQ  age  but  not  to  reach  the  drainage  on  the  other  side  of 

Fig.  85.   Am-     the  watershed  alluded  to. 
nicola  pallida. 

Amnicola  pallida  Haldeman. 

Amnicola  pallida  Haldeman,  Men.  Limn.,  pt.  iii,  cover  p.  3,  1842,  pt.  viii, 
p.  12,  pi.  I,  fig.  7,  1845.  —  BiNNEY,  Land  and  Fw.  Sh.  N.  Am.,  iii,  p. 
83,  fig.  165,  1865. 

Range.  —  New  York  northward  to  Canada  and  Manitoba. 
Lake  Winnipeg,  Brandon,  and  Fine  Creek,  Manitoba. 


Il8  LAND    AND    FRESH    WATER    MOLLUSKS 

These  northern  localities  are  cited  from  the  literature.  I  have  seen 
no  Manitoban  specimens. 

Amnicola  emarginata  Klister. 

Paludina  obtusa  Lea,  Proc.  Am.  Phil.  Soc,  ii,  p.  34,  1841,  not  of  Troschel, 

1837. 
Paludina  emarginata  KvST^K,  Conch.  Cab.,  ed.  11,  Mon.  Paludma,  p.  50,  pi. 

X,  figs.  3,  4,  1852. 
Amnicola  cincinnatiensis  Binney,  Land  and  Fw.  Sh.  N.   Am.,  iii,  p.   85,  fig. 
169,  1865,  not  of  Anthony  ? 

Range.  —  Ohio  and  northward  to  Moose  River,  Hudson  Bay. 

Red  River  of  the  North ;  Manitoba ;  lower  Sas- 
katchewan, near  Lake  Winnipeg !  Moose  Factory  ! 
N.  Lat.  51°  on  Hudson  Bay. 

More  or  less  confusion  has  existed  between  the  va- 
rious shells  which  have  carried  the  specific  name  cin- 
cinnatiensis in  this  family.     The  present  species  is 
Fig.  86.    Am-     the  small  shell  with  a  flat  planorboid  apex  which  has 
nicola    emargt-     usually  been  called  Bythinella  obtusa  Lea.     Baker, 

"^  "^  ,^^,^  ^^     In  his  Mollusks  of  the  Chicaeo  Area,  unites  cincin- 
(magnified).  .        .    -r,.  .  ,     ,  •  •  t     1 

natiensts  Binney  with  this  species,     it  does  not  seem 

to  me  to  resemble  the  obtusa  of  Lea,  particularly. 

Amnicola  cincinnatiensis  Anthony. 

Paludina  cincinnatiensis  Anthony,  Boston  Journ.  Nat.  History,  iii,  p.  279,  pi. 

Ill,  fig.  3,  1840. 
Amnicola  ( Cincinnatid)  cincinnatiensis  Baker,  Moll.  Chicago 

Area,    11,  p.  325,  pi.  xxvi,  fig.  14,   1902. 

Range. — New  York  to  Utah,  Texas  to   Hudson 

Bay.     Moose  Factory,  Hudson  Bay  !  ^^«-  ^7-    -4»i- 

r^,      .  ■,        .         riTT-i  T->  •  •  nicola  cinctnnat- 

The  identity  of  the  Hudson  Bay  specimens  is  ap-      .    ^ . 

parently  indubitable.     The  species  is  asserted  by  Pils- 

bry  to  occur  in  Texas  and  at  various  points  in  the  basin  of  Great  Salt 

Lake,  Utah. 

Genus  Lyogyrus  Gill. 

Lyogyrus  granum  Say.? 

Paludina  granaS>xv,  Journ.  Acad.  Nat.  Sci.  Phila.,  11,  p.  378,  1822. 
Amnicola  granum  Haldeman,   Mon.   Limn.,  viii,  p.    17,  1845. — Binney, 
Land  and  Fw,  Sh.  N.  Am.,  iii,  p.  86,  fig.  170,  1865. 

Range.  —  Virginia  northward  to  the  Great  Lakes  and  Manitoba.? 
Pennsylvania  (Say).     Pine  Creek,  Manitoba  (Miller  Christy). 

Dr.  Pilsbry,  in  the  Nautilus  (xii.  No.  4,  p.  42,  1898),  says  that  the 
Canadian  and  northwestern  specimens  are  not  of  the  same  species  as 


FAMILY    AMNICOLID^  II9 

Say's  Pennsylvania  type.     The  above  range  is  taken  from  the  litera- 
ture ;  not  having  seen  Manitoba  specimens  I  am  unable  to  determine 
what  species  they  represent,  but  it  appears  that  there 
is  a  small  species  in  Manitoba  resembling  L. granum.  ^^ 

Genus  Fluminicola  Stimpson.  ^^°-  ^^-  ^y*' 

gyrus  granum, \. 

Fluminicola  nuttalUana  Lea. 

Paludina  nuttalliana  Lea,  Trans.  Am.   Phil.  Soc,  vi,  p.  loi,  pi.   xxiii,  fig. 

109,  1839. 
Paludina  seminalis  Hinds,  Zool.  Sulphur  Voy.  Moll.,  p.  59,  pi.  xvi,  fig.  22, 

1844. 
t  Amnicola  kt'ndsn  BxiKU,  P.  Z.  S.,  London,  1863,  p.  6y. 


Fig.  89.     JFluminicola  nuttalliana,  \.         Fig.  90.     Fluminicola  hindsii  "BaxrA,  \. 

Range.  —  California  to  British  Columbia.  Variety  hindsii  in  Koo- 
tenai River  and  Wigwam  River,  at  the  foot  of  the  Rocky  Mountains, 
at  an  elevation  up  to  4,626  feet. 

I  have  not  seen  any  British  Columbian  specimens  and  accept  the 
identity  of  F.  hindsii  and  nuttalliana  on  Mr.  Binney's  authority. 
According  to  Dr.  Pilsbry  this  species  is  common  to  the  Columbia 
River  drainage  of  British  Columbia  and  the  United  States. 

Fluminicola  yirens  Lea. 

Paludina  virens  Lea,  Trans.  Am.  Phil.  Soc.,  vi,  p.  91,  pi. 

XXIII,   fig.   93,  1839. 
Paludina  nuclea  Lea,  op.  cit.,  p.  91,  pi.  xxiii,  fig.  103,  1839. 

Range.  — Oregon,  Willamette  River,  Washington, 
Fig.  91.  Flum-  ,  ,7.  t  1      j 

...        .  and  Vancouver  Island. 

intcola   vtrens 

(magnified).  ^^  *^^^  instance  the  Vancouver  habitat  is  cited  from 

the  literature. 

Genus  Pomatiopsis  Try  on. 
Pomatiopsis  lapidaria  Say. 

Cyclostoma  lapidaria  Say,  Joum.  Acad.  Nat.  Sci.  Phila.,  i,  p.  13,  18 17. 
Amnicola  lapidaria  Haldeman,  Men.  Limn.,  viii,  p.  18,  pi.  i,  fig.  10,  1845. 
Pomatiopsis  lapidaria  Tryon,  Proc.  Acad.  Nat.  Sci.   Phila.,  for  1862,  p.  452 

(name  only).  —  Stimpson,  Smithsonian  Misc.  Coll.,  Men.   Hydrobiinae, 

pp.  29-36,  figs.  22-26,  1865. 


I20  LAND    AND    FRESH    WATER    MOLLUSKS 

Paludina  lustrica  Say,  Journ.  Acad.  Nat.  Sci.  Phila.,  ii,  p.  175,  1821. 

Pomatiopsis  lustrica  Binney,  Land  and    Fw.  Sh.  N.  Am., 
Ill,  p.  94,  fig.  189,  1865,  Cayuga  Lake,  N.  Y. 

Range.  —  Eastern  North  America  from  Georgia  to 
Iowa  and  Hudson  Bay. 

Fig.  92.    Po-         Moose  Factory,  N.  Lat.  51°,  on  Hudson  Bay. 
tnatiopsis     laii-  rr^.  .  .,  ,,  <-,.,. 

daria  Say  ^^^  ^^  some  doubt  as  to  whether  Say's  lustrica 

is  the  young  of  his  lapidaria  or  not.  I  have  fol- 
lowed the  general  usage  in  uniting  them.  If  they  should  prove  dis- 
tinct it  is,  according  to  Mr.  Binney,  the  P.  lustrica  which  occurs  in 
the  Northwest  and  on  the  watershed  south  of  Hudson  Bay. 

Family  VALVATIDJE. 
Genus  Valvata  MuUer. 

Valvata  Muller,  Hist.  Verm.,  11,  p.  198,  1774  ;  sole  ex.  V.  cristata  MuUer, 
Europe;  Zool.  Dan.  Prodr.,  p.  239,  1776. — Draparnaud,  Tableau, 
pp.  30,  42,  1801  ;  Hist.  Moll.  Terr,  et  Fluv.  France,  pp.  26,  28,  41, 
1805. — RoissY,  Hist.  Nat.  Moll.,  v,  p.  379,  1805. — Lamarck,  Hist. 
An.  s.  Vert.,  vi,  2,  p.  171,  1822. 

Valvata -\-  Valvearus  Dum^ril,  Zool.  Anal.,  p.  164,  1806. 

(.?)  Cincinna  Hubner,  Zwei  Briefe,  i,  18 10,  fide  Menke,  in  Herrmannsen, 
Ind.  Gen.  Mai.  Suppl.,  p.  50,  1852. 

Gyrorbis  YiTZi^GKK,  Verz,  p.   117,  1833;  type  .?.?  <rm/a/«  Muller. 

"y^  Valvata    Fitzinger,  Verz,  p.  117,  1833;  type  V.  piscinalis  i^xiHAex). 

Planella  Schluter,  Syst.  Verz.  Conchyliensammlung,  p.  13,  1838;  sole  ex. 
Valvata  cristata  Muller. 

Volvata  Berge,  Conch.  Buch,  pp.  17,  20,  26,  1847  ;  err.  typ.f 

Tropidina  H.  and  A.  Adams,  Gen.  Rec.  Moll.,  i,  pp.  343,  344,  1854,  type 
V.  tricarinata  Lesueur,  N.  Am. 

Concinna  '  Hubner,  '  y?^^  H.  and  A.  Adams,  op.  cit.,  p.  343,  1854. 

>  I^/z/a/a  Schluter,  op.  cit.,  p.  13,  1854;    V.  piscinalis  Y€r. 

>  Cincinna  MoRCH,   Vidensk.   Meddel.  for  1863,  p.  321,  1864. — Wester- 

LUND,   Fauna  Pal.    Reg.,  vi,  pp.    131,  132,    1886.     (Type    V.  piscinalis 
Muller  ?) 

>  Tropidina  Morch  (not  Adams),  Vidensk.  Meddel.  Kjob.,  for  1863,  p.  320, 

1864,   V.  minuta  Drap.,  ist  sp. 

>  7^/jy^/a  Bourguignat,  Descr.  Nouv.  Gen.  Alg.,  1877,  V.  Jelskii  Crosse,  1863, 

Russia,  named  for  Prof.  Jelski,  of  Kieff. 
^/elsh'a  Westerlund,   Fauna  Pal,   Reg.,  vi,  p.  143,  1886;  not  ofTacza- 
novich,  Arachnida,   187 1. 

>  (7yr<7r^/5  Westerlund,  Fauna  Pal.  Reg.,  vi,  p.  142,  1886. 

This  genus  has  been  subdivided,  according  to  the  form  of  the  shell, 
into  the  following  sections,  which  appear,  however,  to  have  very  little 
value. 

Valvata  %.s.  {Gyrorbis  Fitz.)  Shell  planorboid  or  depressed, 
without  spiral  keels.     Type   V.  cristata  Muller. 

Cincinna  Morch  (  Valvata  Fitz.).     Shell  turbinate,  with  a  mod- 


FAMILY    VALVATID^  121 

erate  number  of  whorls  slowly  enlarging  and  without  spiral  keels. 
Type  V.  piscinalis  (Miiller) . 

lelskia  Bourguignat  {^Jelskia  West.,  not  Tacz.).  Shell  turbinate, 
with  few  rapidly  enlarging  whorls  and  no  spiral  keels.  Type  V. 
jelskii  Crosse. 

Tropidina  H.  and  A.  Adams.  Shell  depressed  turbinate,  with  the 
upper  surface  of  the  spire  more  or  less  flattened  and  the  whorls  spi- 
rally keeled.     Type   V.  tricar inata  (Lesueur)  Say. 

Since  Miiller  associated  but  one  species  with  the  genus  when  de- 
scribed, that  species  necessarily  becomes  the  type.  A  failure  to  rec- 
ognize this,  when  subdividing  the  genus,  is  responsible  for  several  of 
the  synonyms.  I  have  not  been  able  to  consult  Hiibner's  Zwei  Brief e, 
and  cite  him  on  the  authority  of  Westerlund,  but,  judging  by  his  paper 
on  Cobresia  of  the  same  year,  his  nomenclature  was  not  Linnean, 
although  his  artistic  capacity  seems  to  have  been  exceptional. 

Valvata  tricarinata  Say. 

Cyclostoma  tricarinata  Say,  Joum.  Acad.  Nat.  Sci.  Phila.,  i,  p.  13,  1817. 
Valvata  tricarinata  Say,   op.  cit.,   11,  p.    173,    1821. — Gould,    Inv.  Mass., 

p.  225,  fig.   156,  three  views,  1841. — Haldeman,  Mon.  Limn.,  viii,  p. 

3,  pi.  I,  figs.  1-4,  1845. 
Valvata  carinata  Sowerby,  Genera,  part  xli,  fig.  2,  1834. 
Valvata  unicarinata  De  Kay,  Zool.  N.  Y.,  Moll.,  p.  118,  pi.  vi,  fig.  129,  1843. 
Valvata  tricarinata  var.  simplex  GquLj>,  Inv.   Mass.,  p.  226,   fig.    156  (right 

hand  figure),  1841. 
Valvata  humeralis  Miles,  Geol.  Surv.  Michigan,  p.  237,  i860,  not  of  Say. 
Valvata  tricarinata  var.  confusa  Bryant  Walker,  Nautilus,  xv,  No.   11,  p. 

124,  fig.  2,  1902. 

Range,  —  From  New  England  and  Virginia  westward  to  the  Mis- 
souri, and  northward. 

Type  :  St.  Lawrence  River  and   the  Great  Lakes  !  Manitoba,   in 
Great  Playgreen  and  Winnipeg  Lakes  !  and  Pine  Creek ;  Red  Deer, 
Alberta ;    Moose  Factor}',  Keewatin ;    Saskatchewan 
River  !  Great  Slave  Lake  !  Methy  Lake  in  Lat.  57°  N.  .,- 

Variety    simplex :      English     River,     Keewatin !  ^^^ 

Peace  River,  Athabaska  !     Great  Slave  Lake,  at  Fort 

Resolution  !  upper  Mackenzie  River  at  Fort  Simp-         ^^'  ?^.'     f  ' 
a  vata    tricartna- 

son  !  in  N.  Lat.  62  .  ^^   i_ 

Full  grown  specimens  of  this  species   have   three 
and  a  half   whorls,  a  maximum   diameter  of  5,  and  an  altitude  of  3 
mm.     This   applies   to   both   varieties,    though  under   exceptionally 
favorable  circumstances  it  may  be  somewhat  exceeded.     The  aper- 
ture is   orbicular  and  almost  vertical  in  plane. 


122  LAND    AND    FRESH   WATER    MOLLUSKS 

Valvata  sincera  Say. 

Valvata  sincera  Say,  Rep.  Long's  Exp.,  ii,  p.  264,  pi.  xv,  fig.  11,  1824. 

Range.  —  Northwest  Territory  (Bigsby,  Jide  Say)  southeast  Kee- 
watin  in  Attawapiskat  and  Kawinogans  Rivers  (Mclnnea)  and  the 
southwest  point  of  Anticosti  (McCann) . 

This  shell,  according  to  Say's  original  description  and  figure,  is  "  sub- 
globose-conic  "  with  "nearly  four  whorls,"  "finely  and  regularly 
wrinkled  across,"  with  a  large  umbilicus  "exhibiting  the  volutions,' 
and  a  diameter,  at  right  angles  to  the  axis,  of  slightly  less  than  three 
millimeters,  as  engraved  on  the  plate  in  Long's  Expedition.  I  have 
not  seen  any  shell  corresponding  to  these  characters  from  the  northern 
United  States,  but  Dr.  Whiteaves  has  kindly  sent  me  for  examination 
some  shells  from  southern  Keewatin  and  Anticosti  which  may  prove 
to  be  Say's  sincera.  In  the  literature  and  in  collections  we  find  the 
ecarinate  tricarinata  {simplex  Gould)  and  all  the  non-carinated  forms 
of  the  United  States  generally  labelled  '  sincera  Say,' '  simplex  Gould,' 
etc.  Those  specimens  of  tricarinata  which  preserve  the  '  sul^globose  * 
outline  have  an  umbilicus  smaller  than  the  carinate-  shells  instead  of 
larger.  The  very  flat  and  widely  umbilicate  form  which  is  most  gen- 
erally labelled  sincera^  following  Haldeman's  figures,  is  much  more 
like  the  cristata  of  Europe  than  it  is  like  Say's  shell.  The  specimens 
which  have  been  called  sincera  in  the  literature  of  the  region  we  are 
now  interested  in  are,  so  far  as  I  have  been  able  to  examine  them,  all 
of  the  next  species. 

The  only  shells  in  the  National  Museum  which  at  all  resemble  Say's 
sincera  are  a  series  received  from  Aroostook  County,  Maine,  collected 
by  O.  Nylander,  which  differ  sufficiently  to  be  called  at  least  a  very 
marked  variety. 

Valvata  (sincera  var. .?)  nylanderi  nov. 

Shell  small,  subglobose-conic,  with  four  whorls  of  a  pale  greenish 
straw  color;  surface  polished,  with  faint  spiral  striae,  sculptured 
axially  with  thin,  sharp,  elevated,  rather  distant  lamellae  like  those  on 
Zoogenites  harpa  or  Planogyra  asteriscus  Morse  ;  these  lamellae  are 
closer  and  less  elevated  on  the  apical  part  of  the  shell ;  vertex,  includ- 
ing most  of  the  first  two  whorls,  somewhat  flattish  or  planorboid, 
after  which  the  shell  becomes  subconic ;  the  sutures  deep ;  the  base 
rounded,  with  a  narrow  but  very  deep  umbilicus  ;  plane  of  the  aper- 
ture nearly  vertical,  the  aperture  orbicular,  with  simple  sharp  edges ; 
the  operculum  multispiral,  of  the  same  color  as  the  shell.  Axial  height 
3.2  and  3.4;  diameter  3.5  and  3.7;  diameter  of  umbilicus   .05  and 


FAMILY    VALVATID^  1 23 

.07  ;  of  aperture  i  .5  and  i  .7  mm.,  in  the  broadest  and  narrowest  speci- 
mens, respectively. 

Valvata  lewisi  Currier. 

Valvata  striata  Lewis,  Proc.  Acad.  Nat.  Sci.  Phila.,  for  1856,  p.  260. —  BiN- 
NEY  (as  var.  of  sincerd),  Land  and  Fw.  Sh.  N.  Am.,  iii,  p.  12,  fig.  18, 
1865  ;  not  of  Philippi,  1836. 

Valvata  sincera  Haldeman  {^ro parte),  Mon.  Limn.,  viii,  pL  i,  figs.  6,  7,  8, 

1845. 
Valvata  lewist  Cvkrikk,  List  Moll.  Mich.,  Kent  Sci.  Inst.  Misc.  Pub.,  No.  i, 
p.  9,  1868  ;  new  name  for  V.  striata  Lewis,  not  Philippi. 

Range.  —  Northern  United  States  from  the  Atlantic  to  the  Pacific, 
and  northward. 

New  England  !  Minnesota  !  Colorado  !  Lake  Washington  near  Seat- 
tle !  San  Bernardino  Mountains,  Calif. !  Utah  !  Lake  Superior  !  Anticosti 
Island  !  Pine  Creek,  Manitoba  !  Laggan,  Alberta,  at 
5,200  feet  elevation  ;  Assiniboia  ;  Lake  La  Loche  and 
Peace  River,  Athabaska ;  Great  Slave  Lake !  Fort 
Simpson,  upper  Mackenzie  River,  N.  Lat.  62°!  Fig.  94.  Val- 
Frances  Lake,  head  of  the  Liard  River !  Fort  Chimo,  vata  leivisi  Cur- 
Labrador  !  Sturgeon  Lake,  Athabaska  !  Upper  Colum-  ri^r)  I- 
bia  Lake  !  (Tyrrell) . 

The  name  seems  to  have  been  originally  proposed  for  a  brown  muta- 
tion of  V.  sincera  Haldeman  {non  Say) ,  but  may  well  be  extended  to 
cover  the  whole  species,  which  has  no  other  available  name.  The  shell 
when  normally  developed  and  adult  has  four  whorls  with  a  height  of 
3.6  and  a  diameter  of  5.75  mm.  It  has  a  much  wider  umbilicus  than 
var.  simplex  of  tricarinata  and  is  a  larger  shell,  yet  usually  has  a 
smaller  protoconch.  The  sculpture  is  axial,  fine  and  close,  like  the 
winding  of  thread  on  a  spool.  In  the  typical  form  this  sculpture  is 
coarser  and  more  prominent  than  in  the  less  common  helicoidea.  In 
both  it  is  largely  resident  in  the  periostracum,  the  decorticated  shell 
being  nearly  smooth. 

Valvata  lewisi  var.  helicoidea  nov.    PI.  ii,  figs,  i,  2. 

This  form  resembles  lewisi  but  is  more  depressed,  almost  flat  above, 
and  more  or  less  flattened  toward  the  suture  ;  the  whorls  are  more  slen- 
der and  near  the  aperture  usually  rather  suddenly  expanded ;  the  sur- 
face is  polished,  the  sculpture  frequently  obsolete,  the  umbilicus  wide, 
and  its  bounding  coil  peripherally  diverted  during  the  growth  of  the  last 
half  whorl ;  height  2.5  ;  of  the  aperture  2.0 ;  diameter  of  shell  5.0  mm. 

Range.  —  With  the  type  form,  to  some  extent  ever)rwhere,  but  espe- 
cially toward  the  Northwest.     Lake  Bennett,  Yukon  Territory  !  near 


124 


LAND    AND    FRESH   WATER    MOLLUSKS 


Old  Fort  Yukon,  Alaska  !  thirty  miles  below  Xanana  on  the  Yukon 
River !  Lake  Lindeman ;  East  Kootenai  district,  British  Columbia. 

This  form  is  very  close  to  V.  sibirica  Middendorff ,  wrhich  however 
has  a  more  depressed  apex  and  uniform  fine  sharp  sculpture.  V. 
cristata  is  of  the  same  type,  but  much  smaller. 

Valvata  mergella  Westerlund. 

Valvata  mgrg^e/ZaW^STKRUJiiD,  Vega  Exped.  Vetens.  lakt.,  iv,  p.  209,  pi.  v, 
figs.  22,  a-d,  1885. 

Range.  —  Port  Clarence,  near  Bering  Strait,  Alaska  (Vega)  ; 
Popof  Island,  Shumagins,  in  small  ponds  (Kincaid)  ;  Stewart  River, 
Yukon  district  (Canadian  Geol.  Survey). 

This  is  the  largest  species  of  its  group,  measuring  5  mm.  high  and 
7  mm.  wide,  with  four  whorls.  The  aperture  is  markedly  expanded, 
the  sculpture  very  fine  and  rather  sharp.  The  protoconch  in  the  Shu- 
magin  specimens  is  very  minute.  The  expansion  of  the  aperture  tends 
to  narrow  the  umbilicus,  as  it  were  at  the  last  moment. 

Valvata  virens  Tryon. 

Valvata  virens  Tryon,  Proc.  Acad.  Nat.  Sci.  Phila.,  for  1863,  p.  148,  pi.  i, 
fig.  II. —  BiNNEY,  Land  and  Fw.  Sh.  N.  Am.,  iii,  p.  15,  fig.  21,  1865. 

Range, — Clear  Lake,   California,  to    Vancouver 
Island,  at  Nanaimo. 

A  well  marked  species  of  more  than  usually  tro- 
choid form,  recalling  V.  piscinalis  of  Europe,  but 
large,  more  solid,  and  when  in  good  condition  of  a  pe- 
culiarly elegant  green  tint.  The  figures  given  in 
Tryon's  description  are  of  immature  specimens.  Bln- 
ney  figures  an  adult  specimen  but  does  not  give 
the  measurements. 

Family  VIVIPARID^. 

Genus  Campeloma  Rafinesque. 


Fig.  95.  Val- 
vata virens  Try- 
on,  operculum, 
magnified. 


Fig.  96.     Campeloma  decisum  ;  b,  operculum. 


FAMILY    VIVIPARID^  1 25 

Campeloma  decisum  Say. 

Limncea  decisa  Say,  Nicholson's  British  Encyclopedia,  ist  Am.  ed.,  pi.   ill, 

fig.  6,  1817. 
Paludina  decisa  Sx\,  op.   cit.,   3d    ed.,   pi.   ill,  fig.  6,  1819.  —  Haldeman, 

Men.  Limn.,  Paludina,  p.  4,  pi.  i,  1840. 
Melantho  decisa  Binney,  Land  and  Fw.  Sh.  N.  Am.,  iii,   p.  41,  figs.   79-82. 

1865. 

Range.  —  Eastern  North  America  from  the  Rio  Grande  to  Nova 
Scotia,  west  to  Nebraska,  north  to  the  Saskatchewan.  Lake  Superior 
to  the  Saskatchewan  (Richardson)  ;  Lake  of  the  Woods,  Manitoba, 
(rare,  Hanham). 

It  is  not  unlikely  that  the  extension  of  the  range  of  this  species  as 
far  north  as  the  Saskatchewan  is  unwarranted,  so  many  of  the  data  in 
Sowerby's  list,  in  Richardson,  seem  erroneous,  but  the  presence  of  the 
species  in  the  Lake  of  the  Woods  seems  authentic. 

NAIADES. 

In  discussing  the  Naiades,  the  arrangement  proposed  by  Mr.  Chas. 
T.  Simpson,  in  his  recent  Synopsis  of  the  Naiades,^  is  adopted,  which 
see  for  fuller  synonymy. 

Genus  Lampsilis  Rafinesque. 

Lampsilis  ventricosus  Barnes. 

65»w  7/^«/nVo5»j  Barnes,  Am.  Joum.  Sci.,   ist  sen,  vi,  p.  267,  pi.  xiii,  fig, 

14,  1823. 
Lampsilis  ventricosus  Simpson,  Synopsis,  p.   526,  1900. 

Range. —  Entire  Mississippi  drainage,  the  St.  Lawrence  system, 
southern  drainage  into  Hudson  Bay. 

Lake  Winnipeg;  Battle  River,  Manitoba,  and  north  to  Nelson 
River !  and  its  tributaries,  in  north  latitude  57". 

I«ampsilis  luteolus  Lamarck. 

Unio  luteola  Lamarck,  Anim.  s.  Vert.,  vi,  p.  79,    1819. — Sowerby,  Conch. 

Icon.,  XVI,  Mon.   Unio,  pi.  LViii,  figs.  293,  a-b,  1867. 
Lampsilis  luteolus  Simpson,  Synopsis,  p.  534,  1900. 

Range.  —  Entire  Mississippi  drainage  and  southwest  to  the  Brazos 
River,  Texas ;  entire  Dominion  of  Canada  east  of  the  Rocky  Moun- 
tains and  north  to  the  Red  River  of  the  North  ! 

Lake  Winnipeg !  Lower  Saskatchewan !  Battle  River,  Manitoba. 
Hill  River,  Keewatin !  (var.  superiorensis  Marsh) .  Great  Slave 
Lake  !  Lake  Athabaska  !  Moose  Factory,  James  Bay  !  Manitoba  Lake. 

1  Proceedings  U.  S.  Nat.  Museum,  vol.  xxii,  pp.  501-1044,  1900.  Separate 
paper  No.  1205,  with  pp.  i-viii  prefixed. 


126  LAND    AND    FRESH   WATER    MOLLUSKS 

Lampsilis  borealis  Gray. 

Unio  borealis  Gray,  Ottawa  Naturalist,  1882,  p.  53,  plate  with  three  figures. 
Lampsilis  borealis  (Gray)  Simpson,  Synopsis,  p.  535,  1900. 

Range.  —  St.  Lawrence  drainage.  Lake  of  the  Woods!  Ottawa, 
Ontario  ! 

Lampsilis  radiatus  Gmelin. 

Mya  radiata  Gmelin,  Syst.  Nat.,  vi,  p.  3220,  1792. 

Unio  radiatus  Spengler,  Skr.  Nat.  Selsk,  11,  p.  3,  1792  ;  iii,  p.  62,  1793.  — 

Conrad,  Mon.,  11,  p.  24,  pi.  x,  fig.  2,  1836. 
Lampsilis  radiatus  Simpson,  Synopsis,  p.  535,  1900. 

Range.  —  St.  Lawrence  and  Atlantic  drainage,  south  to  North 
Carolina.     Manitoba. 

Lake  Winnipeg !  Saskatchewan  River !  Nelson  River  drainage ! 
Great  Slave  Lake  (Kennicott)  ! 

Lampsilis  ligamentinus  Lamarck. 

Unio  crassus  Say,  Nicholson's  Encycl.,  Am.  ed.,  11,  Art.  Conchology,  pi.  i, 

fig.  8,  1817.     Not  Unio  crassus  Retzius,  1788. 
Unio  ligamentina  Lamarck,   Anim.   s.  Vert.,  vi,    p.   72,    18 19. — Kuster, 

Conch.  Cab.,  Mon.  Unio,  p.  23,  pi.  iii,  fig.  3,  1852. 
Lampsilis  ligamentinus  Simpson,  Synopsis,  p.  539,  1900. 

Range.  —  Mississippi  drainage,  irregularly  distributed  in  the  St. 
Lawrence  drainage. 

Roseau  River  and  Millwood,  Assiniboine  River,  Manitoba. 

Lampsilis  rectus  Lamarck. 

Unio  recta  Lamarck,   Anim.   s.   Vert.,  vi,  p.    74,    1819. —  Kuster,    Conch. 

Cab.,  Mon.  Unio,  p.  35,  pi.  vi,  fig.  i,  1852. 
Lampsilis  rectus  Simpson,  Synopsis,  p.  544,  1900. 

Range.  —  Entire  drainage  of  the  Mississippi  and  Alabama  Rivers  ; 
St.  Lawrence  system,  Red  River  of  the  North,  Roseau  and  Assiniboine 
Rivers  in  Manitoba ! 

Lampsilis  ellipsiformis  Conrad. 

Unio  ellipsiformis  Conrad,  Mon.,  viii,  p.  60,  pi.  xxxiv,  fig.  i,  1836. 

Unio  spatulatus  Lea  (1845),  Trans.  Am.  Phil.  Soc,  x,  p.  80,  pi.  viii,  fig.  22, 

1848. 
Lampsilis  ellipsiformis  Simpson,  Synopsis,  p.  557,  1900, 

Range.  —  Mississippi  drainage  north  of  Lat.  38°,  St.  Lawrence 
drainage,  in  part ;  Manitoba. 

Red  River  of  the  North  !  Lake  Winnipeg,  Manitoba. 

Lampsilis  alatus  Say. 

Unio  alatus  Say,  Nicholson's  Encycl.,  ist  Am.   ed.,  Art.  Conchology,  11,  pi. 
IV,  fig.  2,  1817. — Conrad,  Mon.,  vii,  p.  57,  pi.  xxxi,  1836. 


FAMILY   UNIONID^  137 

Lampsilis  {Propterd)  alatus  Simpson,  Synopsis,  p.  567,  1900. 

Range.  —  Entire  drainage  of  the  St.  Lawrence;  of  the  Mississippi 
north  of  Arkansas  ;  Alabama ;  Manitoba.     Red  River  of  the  North  ! 

Lampsilis  gracilis  Barnes. 

Unio  gracilis  Barnes,  Am.  Joum.  Sci.,  ist  ser.,  vi,  p.  274,  1823. — Sowerby, 

Conch.  Icon.,  xvi,  pi.  xxxix,  fig.  215,  1866. 
Lampsilis  gracilis  SlMVSO'ii,  Synopsis,  p.  573,  1900. 

Range.  —  Eastern  Texas;  Mississippi,  and  St.  Lawrence  drainage; 
Manitoba.     Red  River  of  the  North  ! 

Genus  Strophitus  Rafinesque. 

Stxophitus  rugosus  Swainson. 

Anodon  rugosus  Swainson,  Zool.  111.,  ist  ser.,  11,  pi.  xcvi,  1822. 
Alasmodonta  edentula  Say,  New  Harmony,  Diss.,  li.  No.  22,  p.  340,  1829. 
Anodonia  edentula  Ykkvssac,  Mag.  de  Zool.,  Guerin,  1835,  p.  25. 
Strophitus  edentulus  Conrad,  Proc.  Acad.  Nat.  Sci.  Phila.,  vi,  p.  263,  1853. 
Anodonta  undulata  Hildreth,  Am.  Joum.  Sci.,  xiv,  p.  290,  1828. 
Anodon  areolatus  Swainson,  Zool.  111.,  2d  ser.,  i,  pi.  xviii,  1829. 
Anodonta  ivardiana  Lea  (1836),  Trans.  Am.   Phil.  Soc,  vi,  p.  46,  pi.  xiv, 

fig.  42,  1838. 
Anodonta  tetragona  Lea  (1845),  op.  cit.,  x,  p.  82,  pi.  vili,  fig.  25,  1845. 
Anodonta  arkansasensis  Lea,  op.  cit.,  xi,  p.  293,  pi.  xxix,  fig.  56,  1852. 
Anodonta  shafferiana  Lea,  op.  cit.,  x,  p.  288,  pi.  xxvi,  fig.  50,  1852. 
Anodonta  showalteri  Lea  (i860),  Journ.  Acad.  Nat.  Sci.  Phila.,  1862,  p.  215, 

pi.  xxxiii,  fig.  284,  1862. 
Alasmodon  rhombica  Anthony,  Am.  Joum.  Conch.,  i,  p.  158,  pi.  12,  fig.  5, 

1865. 
Anodonta  salmonca  Ct-KSSm,  Conch.  Cab.,  Mon.  Anodonta,  p.  91,  pi.  xxiv, 

figs.  1-2,  1873. 
Anodonta  pavonia  Lea. 

Range.  —  St.  Lawrence  system;  the  whole  of  the  Mississippi 
drainage,  Texas,  Alabama,  the  Atlantic  drainage  ;  Manitoba. 

Red  River  of  the  North  !  Lake  Winnipeg  !  Great  Playgreen  Lake  ! 
Saskatchewan  River. 

Genus  Anodonta  Lamarck. 
Anodonta  beringiana  Middendorff. 

Anodonta  cettensis  var.   beringiana  Midd.,  Sib  Raise,  11,  p.  284,  pi.   xxviii, 

figs.  4-7,  pi.  XXIX,  figs.   1-4,  1 85 1. 
Anodonta youconensis  Lea,  Proc.  Acad.  Nat.  Sci.  Phila.,  xi,  p.  81,  1867. 
Anodonta youkanensis  Lea,  Joum.  Acad.  Nat.  Sci.  Phila.,  n.  s.,  vi,  p.  287,  pi. 

XL,  fig.  99,  1868. 

Range.  —  Drainage  into  Bering  Sea  from  Asia  and  America ;  also 
Cook  Inlet  drainage. 

Kenai  Peninsula !  Kuskokwim  River  near  Redoubt  Kolmakof ! 
Yukon  River  below  Anvik,  in  pools  and  quiet  sloughs  left   by   the 


128  LAND    AND    FRESH   WATER    MOLLUSKS 

receding  freshets  !    Avacha  Bay,  Kamchatka  !    Amur  River !  eastern 
Siberia  and  Mongolia. 

Anodonta  kennerleyi  Lea. 

Anodonta  kennerleyi  "Lex,   Proc.   Acad.  Nat.  Sci.  Phila.,  iv,  p.   306,  i860; 
Journal,  v,  p.  108,  pi.  xviii,  fig.  256,  1862. 

Range.  —  Puget  Sound  !  British  Columbia. 

Anodonta  oregonensis  Lea. 

Anodonta  oregonensis  \jE.h.,  Trans.  Am.  Phil.  Soc,  vi,  p.  80,  pi.  xxi,  fig.  67, 

1838. 
Margarita  {Anodonta)  oregonensis  Lea,  Synopsis,  p.  30,  1837. 
Anodonta  cognata  Gould,   Proc.   Boston  Soc.   N.   Hist.,  iii,  p.   294,  1850; 

Rep.  on  Moll.  U.  S.  Expl.  Exp.,  p.  435,  pi.  xxxviii,  figs.  546,  a-b,  1852. 

Range.  —  Northern  California,  Oregon  and  British  Columbia ; 
eastward  to  Great  Salt  Lake,  Utah. 

Vancouver  Island,  B.  C,  abundant  near  Victoria,  and  at  Nootka; 
Sumas  Lake,  Fraser  River  valley,  B.  C.  Shush wap  Lake ;  Nicola 
Lake  and  Okanogan  Lake,  B.  C. ;  Kadiak  Island,  Alaska  (Fisher). 

Anodonta  nuttalliana  Lea. 

Anodonta  nuttalliana  Lea,  Trans.  Am.   Phil.  Soc,  vi,  p.  tj,  pi.  xx,  fig.  62, 

1838. 
Anodonta  triangularis  Trask,  Proc.  Acad.  Nat.  Sci.  Calif.,  I,  p.  29,  Feb.  19, 

1855. 
Anodon  triangularis  Sowerby,  Conch.  Icon.,  xvii,  pi.  xxix,  fig.  56  b,  1870. 

Range.  —  California  in  the  Sacramento  River,  and  northw^ard  to 
British  Columbia,  Nootka  and  Clayoquot  Sound,  Vancouver  Island ; 
Chilliwak  Lake,  Nicola  Lake  and  Shushwap  Lake,  British  Columbia. 

Anodonta  wahlamatensis  Lea. 

Anodonta  wahlamatensis  Lea,  Trans.  Am.  Phil.  Soc,  vi,  p.  78,  pi.  xx,  fig. 

64,  1838. 
Anodonta  rotundovataTvLASm,  Proc.  Acad.  Nat.  Sci.  Calif.,  i,  p.   29,  1855. 
Anodon  rostratus  Sowerby,  Conch.  Icon.,  xvii,  pi.  11,  fig.  4,   1872. 
Anodonta  laosensis  Fischer,  Bull.  Soc  N.  Hist.,  d'Autun,  p.  219,  1891. 
Anodonta  rotundata  Simpson,  Synopsis,  p.  629,  in  synonymy,  1900,  not  of 

Trask. 

Range.  —  Utah  and  westward,  California  to  British  Columbia  in 
the  Pacific. 

Nootka,  Vancouver  Island  ;  Sumas  Lake  and  Prairie,  Fraser  River 
valley,  British  Columbia. 

Anodonta  marginata  Say. 

Anodonta  marginata  Say,  Nicholson's  Encyclop.,  ist  Am.  ed.,  11,  Art.  Con- 
chology,  p.  19,  pi.  Ill,  fig.  5,  1817. 


FAMILY    UNIONID^  1 29 

Atiodonta  fragilis  Lamarck,  Anim.  s.  Vert.,  vi,  p.  85,  1819. — Delessert, 

R6c.  Coq.  Lam.,  pi.  xiii,  figs.  2a,  2^,  1841. 
Anodonta  lacustris  Lea,  Proc.  Acad.  Nat.  Sci.  Phila.,  I,  p.  84,  1857. 
Anodonta  flava,  pallida,  glandulosa  and  irisans  Anthony,  Am.  Journ.  Conch., 

I,  pp.  1 6 1-3,  pi.  xiv-xvi,  1865. 
Anodonta  subcarinata  Currier,  Am.  Journ.  Conch.,  iii,  p.  113,  pi.  vi,  fig.  5, 

1867. 
Anodon  exilis  Sowerby,  Conch.  Icon.,  xvii,  pi.  xxii,  fig.  84,  1869. 

Range.  —  Drainage  of  the  St.  Lawrence  River  basin,  including  the 
lakes. 

Anticosti  Island,  in  lake  near  Becsia  River,  six  miles  inland  !  Battle 
Creek,  Manitoba ! 

Anodonta  implicata  Say. 

Anodonta  implicata  Say,  New  Harmony,  Diss.,  11,  No.  22,  p.  340,  1822. — 
Clessin,  Conch.  Cab.,  ed.  11,  Anodonta,  p.  78,  pi.  xix,  fig.  3,  1873. 

Anodonta  neivtonensis  Lea,  Trans.  Am.  Phil.  Soc. ,  vi,  p.  79,  pi.  xxi,  fig.  66, 
1838. 

Anodonta  housatonica  Linsley,  Am.  Journ.  Sci.,  1845,  p.  277. 

Range,  —  Atlantic  drainage  from  Virginia  northward,  St.  Law- 
rence drainage,  Saskatchewan  basin. 

Manitoba  in  Lake  Winnipeg !  and  Souris  River ;  lower  Saskatche- 
wan River ! 

Anodonta  grandis  Say. 

Anodonta  grandis  Say,  New  Harmony,  Diss.,  11,  p.  341,  1829. — Clessin, 

Mon.  Anod.  in  Conch.  Cab.,  n.  ed.,  p.  96,  pi.  xxx,  figs.  1-2,  1873. 
Anodonta  ovata  Lea,  Trans.  Am.  Phil.  Soc,  vi,  p.  2,  pi.  11,  fig.  2,  1838. 
Anodonta  salmonea  Lea  (pathologic).  Trans.  Am.   Phil.  Soc,  vi,  p.  45,  pi. 

XIV,  fig.  41,  1838. 
Anodonta  lewisii  Lea,  Journ.  Acad.   Nat.  Sci.  Phila.,  iv,  p.  362,  pi.  LXii, 

fig.  187,  i860. 
Anodonta  footiana  Lea,  Trans.  Am.  Phil.  Soc,  viii,  p.  225,  pi.  xx,  fig.  44, 

1842. 
Anodonta  marryattiana'LE.x,  op.  cit.,  p.  226,  pi.  xx,  fig.  45,  1842. 
Anodonta  gigantea  Lea,   Trans.   Am.   Phil,   Soc.  1834,  p.    1,   pi.    I,   fig.    i 

(pathologic  ?  ). 
Anodonta  grandis  Simpson,  Synopsis  Naiades,  pp.  641-644,  1900  (with  many 

synonyms). 

Range.  —  Entire  Mississippi  system  and  southwest  to  Texas  ;  up- 
per St.  Lawrence  drainage  ;  Manitoba. 

Red  River  of  the  North !  Shoal  Lake ;  Souris  River !  Fairford 
River  !  and  Lake  Winnipeg,  Manitoba  ! 

Variety  footiana  Lea  :  Souris  River,  Manitoba  1  Nipegon  River, 
Lake  Hannah. 

\diX\sXy  gigantea 'L.^Q.'.  Manitoba. 

This  variable  and  widely  extended  species  is  responsible  for  many 
synonyms  cited  by  Mr.  Simpson.     It  appears  that  the  Manitoba  and 


130  LAND    AND    FRESH    WATER    MOLLUSKS 

perhaps  the  upper  St.  Lawrence  localities  may  owe  its  presence  to 
capture  of  part  of  the  Mississippi  drainage,  owing  to  changes  of  level, 
elsewhere  referred  to. 

Anodonta  kennicotti  Lea. 

Anodonta  kennicotti  Lea,  Proc.  Acad.  Nat.  Sci.  Phila.,  v,  p.  56,  1861  ;  Jour- 
nal, n.  s.,  V,  p.  214,  pi.  XXXIII,  fig.  283,  1862. 

Anodonta  simpsoniana  Lea,  op.  cit.,  p.  56,  1861  ;  p.  212,  pi.  xxxii,  fig. 
281,  1862. 

Anodonta  dallasiana  Lea,  Proc.  Acad.  Nat.  Sci.  Phila.,  vii,  p.  190,  1863  ; 
Journal,  vi,  p.  29,  pi.  xi,  fig.  28,  1866. 

Range.  —  Upper  and  middle  St.  Lawrence  system.  Mackenzie 
drainage  to  Great  Slave  Lake. 

Lake  of  the  Woods ;  Manitoba  Lake ;  Lake  Winnipeg  !  Grand 
Rapids  of  the  Saskatchewan  !  Ekwan  River,  Keewatin ;  Fort  Simp- 
son, Mackenzie  River  !  Fort  Erie  and  Fort  Rae  !  Great  Slave  Lake  ; 
Buffalo  Lake,  Methy  Portage,  Saskatchewan. 

This  is  the  most  characteristic  Naiad  of  the  central  Boreal  region 
and  reaches  perhaps  farther  north  (Lat.  63°)  than  any  other  species  in 
American  waters. 

Anodonta  pepiniana  Lea. 

Anodonta pepiniana  Lea,  Trans.  Am.  Phil.  Soc,  vi,  p.  96,  pi.  xvi,  fig.  51,  1838. 

Range.  —  Upper  and  middle  St.  Lawrence  drainage,  Saskatche- 
wan basin. 

Lake  Winnipeg  !  Manitoba.    Attawapiskat  River,  eastern  Keewatin. 

Genus  Gonidea  Conrad. 

Gonidea  angulata  Lea. 

Anodonta angulaia'LEA,  Trans.  Am.  Phil.  Soc,  vi,  p.  97,  pi.  xvi,  fig.  52,  1838. 
Anodon  feminalis  Gould,  Proc.  Boston  Soc.  N.  Hist.,  iii,  p.  293,  1850  ;  MolL 

U.  S.  Expl.  Exp.,  p.  436,  pi.  xxxviii,  figs.  547,  a-b,  1852. 
Anodonta  randalli  Tkask,  Proc.  Acad.  Nat.  Sciences  Calif.,  i,  p.  28,  1855. 
Anodon  h'an^^u^ata Sowerby,  Conch.  Icon.,  xvii,  pi.  xxiii,  figs.  8,  a-3,  1869. 

Range.  —  Central  California,  north  to  British  Columbia  and  east- 
ward to  Idaho. 

Columbia  River  near  Fort  Colville  ! 

This  singular  shell  hardly  more  than  crosses  the  boundary,  so  far  as 
reported.  According  to  Stearns  and  Hemphill  this  species  buries  itself 
obliquely  in  the  rather  hard  bed  of  rapid  streams,  so  that  the  flattened 
posterior  portion  lies  horizontally  even  with  the  bottom,  and  offers  no 
resistance  to  the  current.  Whether  the  flattening  and  consequent  angu- 
lation of  the  valves  is  a  modification  due  to  the  burrowing  habit  and 
the  influence  of  its  environment,  or  not,  cannot  yet  be  positively  stated. 


FAMILY    UNIONID^  I3I 

Genus  Anodontoides  Simpson. 
Anodontoides  ferussacianus  Lea. 
Anodonta  ferussaciana  Lea,  Trans.  Am.  Phil.  Soc,  v,  p.  45,  pi.  vi,  fig.   15, 

1834. 

Anodonta  buchanensis  Lea,  op.  cit.,  p.  47,  pi.  xiv,  fig,  43,  1838. 
Anodonta  argentea  Lea,  op.  cit.,  viii,  p.  223,  pi.  xix,  fig.  41,  1842. 
Anodonta  ferruginea  Lea,  op.  cit.,  viii,  p.  225,  pi.  xix,  fig.  43,  1842. 
Anodonta  plicata  Haldeman,  Journ.  Acad.  Nat.  Sci.  Phila.,  viii,  p.  201,  1842. 
Anodonta  denigrata  Lea,  Trans.  Am.  Phil.  Soc,  x,  p.   285,  pi.  xxv,  fig.  45, 

1852. 
Anodonta  oblita  Lea,  op.  cit.,  p.  46,  pi.  xxviii,  fig.  52,  1852. 
Anodonta  subcylindracea  Lea,  op.  cit.,  vi,  p.  106,  pi.  xxiv,  fig.  117,  1838. 
Anodonta  modesta  Lea,  Journ.  Acad.  Nat.  Sci.   Phila.,  n.  s.,  iv,  p.   364,  pi. 

LXiii,  fig.  189,  i860. 

Range.  —  Mississippi  drainage,  St.  Lawrence,  Red  River  of  the 

North,  and  Saskatchewan  basins. 

Lake  Winnipeg  !  Lake  of  the  Woods  ! 

Genus  Symphynota  Lea. 
Subgenus  Lasmigona  Rafinesque. 
Symphynota  costata  Rafinesque. 

Alasmidonta  costata  Rafinesque,  Ann.  Gen.  Sci,  Brux.,  v,  p,  318,  pi.  Lxxxii, 

figs.  15,  16,  1820. 
Alasmodonta  rugosa  Barnes,  Am,  Journ,   Sci,,  vi,  p.   278,  pi.   xili,  fig.  21, 

1823. 

Range.  —  Mississippi  and  St.  Lawrence  basins. 
Manitoba  in  Roseau  River  ! 

Subgenus  Pterosygna  Rafinesque. 
Symphynota  complanata  Barnes. 

Alasmodonta  complanata  Barnes,  Am.  Journ.  Sci.,  vi,  p.   278,  pi.  xiii,  fig. 

22,  1823. — Baker,  Moll.  Chicago  Area,  i,  p.   60,  pi.  viii,  figs,  1-2,  pL 

IX,  figs.  1-4,  1898. 
Complanaria  gigas   Sowerby,   Conch.   Manual,  fig.    141,    1839  ;  2d  ed.,  p. 

115,  fig.  141,  1842. 
Unio  katherincE  Lea,   Synopsis,  p.  35,  1838;  Trans.  Am.  Phil.  Soc,  vi,  p. 

143,  1839.     Lake  Superior. 

Range.  —  Mississippi  drainage  north  of  Arkansas  on  the  west  and 
Tennessee  on  the  east ;  Upper  St.  Lawrence  and  its  tributaries.  The 
variety  katherince  northward  from  Lake  Superior  to  the  Mackenzie 
and  Keewatin. 

Lake  Winnipeg !  Shell  River  and  Lower  Saskatchewan !  Nelson 
River  drainage  ;  Assiniboine  River ;  Red  River  of  the  North  !  Battle 
River,  Manitoba, 


132  LAND    AND    FRESH    WATER    MOLLUSKS 

Genus  Margaritana  Schumacher. 
Margaritana  margaritifera  Linne. 
Typical  form ; 

Mya  margaritifera  Linne,  Syst.  Nat.,  ed.  x,  p.  671,  1758,  Conch.  Cab.,  vi,  pi. 

I,  fig.  5- 
Alasmodonta  arcuata 'Qa.'k^te.S,  Am.  Journ.  Sci.,  vi,  p.   277,  pi,  xil,  fig.  20, 

1823. 
Unio  elongatus  Lamarck,  Anim.  s.  Vert.,  vi,  p.  70,  18 19. 
Unto  sinuata  C.  Pfeiffer,  1825  ;  +  U.  roissyi  Michaud,  1831  ;  +  U.  tristis 

Morelet,  1845  \  +  U.  /rra5«>«>««^  (Klein)  Lea,  1836. 
Unio  {Alasmodonta)  dahuricus  Middendorff  (1850),   Sib.  Reise,  il,  p.  275, 

pi.  XXVI,  figs.  3-5,  1851. 
Unio  cotnplanatus  Middendorff,  Sib.  Reise,  11,  p.  273,  pi.  xxvii,  figs.  1-6, 

1851. 
Unio  mongolicus,  Middendorff,  Sib.  Reise,  11,  p.  277,  pi.  xxvii,  figs.  7-8, 

1851. 
Margaritana  margaritifera  Simpson,  Synopsis,  pp.  674-677  {ex  parte),  1900. 

Margaritana  margaritifera  variety  falcata  Gould. 

Alasmodon  falcata  Gould,  Proc.  Boston  Soc.  N.  Hist.,  iii,  p.  294,  Nov., 
1850;  Wilkes'  Expl.  Exp.  Moll.,  p.  433,  figs.  545,  a-b,  1852. 

Unio  falcatus  Sowerby,  Conch.  Icon.,  xvi,  Mon.  Unio,  pi.  lxxv,  fig.  390, 
1868. 

Alasmodon yubaensis  TKASVi,  Proc.  Calif.  Acad.  Sci.,  i,  p.  30,  1855. 

Range  of  the  type.  —  The  whole  of  northern  Europe  and  w^estem 
Siberia.  In  northeastern  Asia  from  the  Upper  Amur  basin  and  south- 
em  Mongolia,  Kamchatka,  and  Sakhalin  Island.  In  America  on  Anti- 
costi  Island ;  Quebec  Province,  eastern  Canada ;  Nevv^  England  and 
Newr  York.  Also,  isolated  from  the  eastern  area  by  a  wide  gap,  in 
the  Lower  Saskatchewan  near  Lake  Winnipeg. 

Range  of  the  variety.  —  California,  in  the  Sierra,  Plumas  Co.,  at 
7,400  feet  above  the  sea  !  Sacramento  River ;  Yuba  River ;  Oregon ; 
Washington  at  Wallawalla  ;  northwestern  Montana  in  the  headwaters 
of  the  Missouri  !  (only)  above  Fort  Benton,  but  not  reported  lower 
down ;  Victoria  and  Nanaimo !  Vancouver  Island ;  Eraser  River ; 
Kakwous  Lake  (4,000  feet  elevation)  and  streams  in  Lat.  50°,  Brit- 
ish Columbia ;  Naha  Bay,  Alaska,  abundant  near  sea  level  in  small 
lake,  Lat.  55^35  North  ! 

The  most  obvious  distinction  between  the  typical  form  and  variety 
falcata  lies  in  the  purple  nacre  of  the  latter,  which  is  often  extremely 
rich  and  beautiful,  though  in  old  cabinet  specimens  usually  much 
faded.  The  specimens  above  the  falls  in  the  headwaters  of  the  Mis- 
souri may  have  been  captured  with  streams  by  orographic  changes, 
or  transported  in  the  glochidium  stage  attached  to  fishes  ;  at  any  rate 


FAMILY    UNIONID^  I33 

they  are  of  the  Pacific  type,  and  are  not  found  below  the  site  of  Fort 
Benton,  so  far  as  yet  reported.  It  is  quite  evident  that  much  scientific 
interest  attaches  to  a  thorough  knowledge  of  the  distribution  of  this 
species,  with  its  possible  relation  to  geologic  changes  and  the  results  of 
glaciation.  It  is  to  be  hoped  that  any  data  bearing  on  this  matter  will 
be  carefully  preserved  and  put  on  record  by  travelers  and  others  in 
these  regions. 

Genus  Unio  Retzius. 

Unio  complanatus  Solander. 

Mya  complanata  Solander  (after  Lister,  t.  1 50,  fig.  5),  in  Cat.  Portland  Mu- 
seum, p.  100,  No.  2190,  1786.  —  DiLLWYN,  Descr.  Cat.  Rec.  Sh.,  i,  p. 
51.  1817. 

Unio  complanatus  Simpson,  Synopsis,  pp.  720-5,  1900. 

Range.  —  Atlantic  drainage  from  Georgia  to  the  St.  Lawrence 
system.     Also  in  the  Saskatchewan  River. 

North  shore  of  Lake  Superior ;  Lake  Nipissing,  etc. 

Genus  Quadrula  Rafinesque. 

Quadrula  plicata  Say. 

Unio  plicata  Say,  Nicholson's  Encycl.,  ist  Am.  ed.,  Art.  Conch.,  pi.  ill,  fig. 

I,  1817. 
Unio  crassus  Barnes,  Am.  Journ.  Sci.,  vi,  p.  118,  1823. 
Quadrula  plicata  Simpson,  Synopsis,  p.  767,  1900. 
Unio  hippopcEus  Lea,  Proc.  Am,  Phil.  Soc.,  iv,  p.  163,  1845  (variety). 

Range.  —  Mississippi  drainage  from  Arkansas  and  Tennessee 
northward ;  Western  Michigan,  Red  River  of  the  North,  Lake  Win- 
nipeg and  the  Saskatchewan. 

The  variety  htppop<ea  occurs  in  Lakes  Erie,  Michigan,  and  Win- 
nipeg. 

Quadrula  undulata  Barnes. 

Unio  undulata  Barnes,  Am.  Joum.  Sci.,  vi,  p.  120,  pL  11,  1823. 
Unio  costatus  Say,  Am.  Conch.,  vi.  No.  41,  1834  ;  not  of  Rafinesque. 
Quadrula  undulata  Simpson,  Synopsis,  p.  769,  1900. 

Range.  —  Mississippi  and  St.  Lawrence  drainage  generally,  Texas 
and  Alabama ;  Red  River  of  the  North ;  Lake  Winnipeg ;  the  Sas- 
katchewan River. 

Quadrula  heros  Say. 

Unio  heros  Say,  New  Harmony  Diss.,  11,  No.  19,  p.  291,  1829. — Conrad, 

Men.,  XII,  p.  107,  pi.  Lix,  1840. 
Unio  multiplicatus  Lea,  Trans.  Am.  Phil.  Soc,  iv,  p.  70,  pi.  rv,  fig.  2,  1831. 

Range.  —  Nuevo  Leon,  Mexico ;  Tombigbee  River,  Alabama.  The 
Mississippi  system  generally  ;  Red  River  of  the  North,  Manitoba. 


134  LAND    AND    FRESH    WATER    MOLLUSKS 

Quadrula  lachrymosa  Lea. 

Unio  lachrymosus  Lea,  Trans.  Am.  Phil.  Soc,  in,  p.  272,  pi.  vi,  fig.  8,  1827. 
Unio  asperrimus  Lea,  op.  cit.,  iv,  p.  71,  pi.  v,  fig.  3,  1831. 
Unio  quadrulus  Say,  Am.  Conch.,  vi,  pi.  Liii,  1834  ;  not  of  Rafinesque. 
Quadrtda  lachrymosa  Simpson,  Synopsis,  p.  776,  1900. 

Range.  —  Entire  Mississippi  drainage;  various  localities  in  the  St. 
Lawrence  system ;  Red  River  of  the  North,  Manitoba,  abundant. 

Quadrula  rubiginosa  Lea. 

Unio  rubiginosus  Lea,  Trans.  Am.  Phil.  Soc,  in,  p.  427,  pi.  viii,  fig.  10, 

1829. 
Unio  fiavus  Conrad,  1834. — Say,  Am.  Conch.,  vi,  1834.  —  Conrad,  Mon., 

IX,  p.  74,  pi.  XII,  fig.  2,  1837. 
Unio  trigonus  Sowerby,   Conch.   Icon.,  Mon.  Unio,  xvi,  pi.  LXlv,  fig.  322, 

1868. 
Quadrula  rubiginosa  Simpson,  Synopsis,  p.  786,  1900. 

Range.  —  Entire  Mississippi  drainage ;  eastern  Texas ;  St.  Law- 
rence drainage  ;  Red  River  of  the  North  !  Manitoba ;  Nelson  River ! 
Keewatin ;  Red  and  Roseau  Rivers  and  Lake  Winnipeg,  Manitoba. 

Family  SPH^RIID^. 

This  family  is  reviewed  in  Trans.  Wagner  Institute,  vol.  in,  part 
VI,  pp.  1439-60,  and  a  summary  of  the  arrangement  adopted  is  also 
given  in  Proceedings  Biological  Society  of  Washington,  xvi,  pp.  5-8, 
1903.  This  arrangement  in  effect  is  that  which  is  adopted  on  the 
present  occasion.  The  specific  synonymy  is  mainly  due  to  the  late 
Temple  Prime,  who  kindly  named  the  Alaskan  specimens  collected 
previous  to  his  death.  Some  later  arrivals  have  been  examined  by  Dr. 
Sterki.  I  have  seen  no  specimens  or  figures  of  the  species  from  Port 
Clarence  named  by  Westerlund,  and  they  are  introduced  on  his  author- 
ity. It  is  probable  that  a  considerable  reduction  will  eventually  be  had 
in  the  number  of  nominal  species,  especially  of  Corneocyclas, 

Genus  Sphaerium  Scopoli. 
Subgenus  Sphaerium  s.  s. 
Sphaerium  simile  Say. 

Cyclas  siniilis  Say,  Nicholson's  Encycl.,  ist  Am.  ed.,  pi.  l,  fig.  9,  18 17. 
Cyclas  sulcata  Lamarck,  Anim,  s.  Vert.,  v,  p.  560,  18 18. 
Spharium  sulcatum  Prime,  Mon.  Am.  Corbie,  p.  33,  fig.  25,  1865. 

Range.  —  United  States,  east  of  the  Mississippi  River;  Canada; 

Manitoba. 

Lake  Superior ;  Red  River  of  the  North ;  Lake  Winnipeg ;  Pine 


FAMILY    SPH^RIID^  I35 

Creek   and  Fort   Pelly,  Manitoba ;    Lower    Saskatchewan   River   at 
Grand  Rapids ! 


Fig.  97.     Sfh(erium  simile  Say. 

This  species  is  the  Cyclas  saratogea  of  Lamarck  and  has  numerous 
other  synonyms.  It  is  the  largest  species  of  the  group  in  North 
America,  but,  judging  by  the  records,  rather  irregularly  distributed. 
The  Lamarckian  locality  is  Lake  George ;  Say's  specimens  are  from 
the  vicinity  of  Philadelphia. 

Sphaerium  striatinum  Lamarck. 

Cyclas  striatina  Lamarck,  Anim.  s.  Vert.,  v,  p.  560,  1818. 

Sphceriutn  striatinum  Prime,  Men.  Am.  Corbie,  p.  37,  fig.  29,  1865. 

Range.  —  North  America  generally,  east  of  the  Sierra  Nevada 
Mountains,  from  Alabama  to  the  L^pper  Mackenzie. 

Hell  Gate  River  (Columbia  drainage) ,  Montana ; 
Humboldt  River,  Nevada  (Hepburn)  ;  in  Manitoba 
at  Lake  Winnipeg ;  Great  Playgreen  Lake  ;  York 
Factory,  Keewatin  ;  Pasqua  Lake,  Assiniboia  ! 
Saskatchewan  River  at  Grand  Rapids  !  Mackenzie 
River  at  old  Fort  Simpson  ! 

So  far  as  the  records  indicate,  the  place  of  this     ^''^-  9^     .  '^^^'^" 

-,,_,,        ,  .  ,  rium  strtattnum. 

species  is  east  of  the  Rockies,  but  in  at  least  two 

places  it  has  been  transferred  to  the  head-waters  of  streams  flowing 

westward.     In  the  East  it  is  perhaps  the  most  common  of  the  Sphceria^ 

taking  much  such  a  place  as  6".  corneum  does  in  the  European  fauna. 

*  Sphaerium  aureum  Prime. 

Cyclas  aurea  Prime,  Proc.  Boston  See.  Nat.  Hist.,  iv,  p.  159,  185 1. 

Sphcerium  aureum  Prime,  Mon.  Am.  Corbie,  p.  35,  fig.  26,  1865. 

Range.  —  Lake  Superior. 

It  is   probable  that  this  species   crosses  the  line  into 
Canada,  though  not  yet  searched  for  in  that  region. 

Sphaerium  walkeri  Sterki.  „,  /°'  V' 

iip  h  (B  rtuin 
Sphcerium  walkeri  Sterki,  Nautilus,  xrv,  p.  142,  April,  1901.       aureum. 


136 


LAND   AND    FRESH    WATER    MOLLUSKS 


Range.  —  Frances  Lake  and  Finlayson  Lake,  Yukon  District,  Liard 
River  drainage  (Dawson);  Lake  Michigan,  12  fathoms  (Walker). 

Identified  by  Dr.  Sterki,  a  species  related  to  rhomboideum  and  occi- 
dentate^  but  yet  unfigured. 

Sphaerium  solidulum  Prime. 

Cyclas  solidula  Prime,  Proc.  Boston  Soc.  Nat.  Hist.,  iv,  p.  158,  185 1. 
SphcErium  solidulum  Prime,  Mon.  Am.  Corbie,  p.  36,  fig.  27,  1865. 

Range.  —  Eastern  United  States,  from  New  Mexico  and  Louisiana 
to  the  Great  Lakes,  and  Manitoba. 

In  Manitoba,  at  Winnipeg,  Brandon,  and  the  Red  River  of  the 
North;  in  Alberta,  at  Egg  Lake. 

Sphserium  stamineum  Conrad. 

Cyclas  starninea  Conrad,   Am.  Journ.  Sci.,  xxv,   p.  342, 

pi.  I,  fig.  5,  1834. 
Sphcerium  stamineum  Price,  Mon.  Am.  Corbie,  p.  38,  fig. 

30,  1865. 

Range.  —  Eastern   United    States,   northward   to 
Manitoba. 

Manitoba  (Hanham). 

The  type  locality  for  this  species  is  Alabama.  In  1865  Mr.  Prime 
united  with  it  the  Cyclas  fuscata  of  Rafinesque  (Ohio)  and  the  C. 
bulbosa  Anthony  from  Arkansas.  Later  collectors  have  found  it 
widely  distributed  over  the  eastern  portion  of  the  continent. 

Sphaerium  rhomboideum  Say. 

Cyclas  rhomboida  Say ,  Journ.  Acad.  Nat.  Sci.  Phila.,  11,  p.  380,  1822. 
Cyclas  elegans  Adams,  Boston  Journ.  Nat.   Hist.,  iii,  p.  330,  pi.  in,  fig.  11, 

1840. 
sphcerium  rhomboideum  Prime,  Mon.  Am.  Corbie,  p.  39,  fig.  31,  1865. 


Fig.  100.  SphcB- 
rium  stamine- 
um Conrad. 


lOi  102  103 

Fig.  ioi.  Sphcerium  rhomboideum  Say. 

Fig.  102.  Sphcerium  dentatum  Hald. 

Fig.  103.  sphcerium  fabale  Prime. 

Range.  —  New  England  to  Michigan,  and  northwestward. 
Lake  Superior ;  Manitoba  at  Pine  Creek  and  in  Lake  Winnipeg. 


FAMILY    SPHyERIID^  I37 

Left  bank  of  the  Yukon  River,  Alaska,  30  miles  below  the  mouth 
of  the  Tanana !     In  duck's  crop  at  Pender  Island,  British  Columbia. 

This  attractive  species  is  apparently  sporadic  or  local  in  its  habitats, 
but  if  intelligently  sought  for  would  probably  be  found  more  often. 
It  is  not  yet  positively  known  from  British  Columbia,  but  there  is  little 
reason  to  doubt  it  will  be  found  there  when  the  fauna  is  better  known. 
So  far  it  seems  to  be  rather  rare  everywhere. 

*Sphaerium  dentatum  Haldeman.      Figure  102. 

Cyclas  dentata   Haldeman,   Proc.  Acad.   Nat.  Sci.  Phila.,  i,  p.   100,   1841, 

Willamette  River,  Oregon. 
Spharium  dentatum  Prime,   Men.  Am.  Corbie,  p.  40,  fig.  32,  1865. 

Range.  —  California  and  Oregon.     Spokane  Falls,  Washington. 

Sphaerium  fabale  Prime.     Figure  103. 

Cyclas  fabalis  Prime,  Proc.  Boston  See.  Nat.  Hist.,  iv,  p.  159,  1851. 
Sphceriutn  fabalis  Prime,  Men.  Am.  Corbie,  p.  40,  fig.  33,  1865. 

Range.  —  Eastern  United  States  and  northward,  Battle  River, 
Alberta. 

This  species  was  originally  described  from  specimens  collected  in 
Lake  Superior  by  Louis  Agassiz,  but  has  since  been  recognized  from 
Georgia,  Virginia  and  Tennessee.  It  is  remarkable  for  its  compressed 
form  and  inconspicuous  beaks. 

Sphaerium  occidentale  Prime. 

Cyclas  ovalis  Prime,  Proc.  Boston  Soc.  Nat.  Hist,  rv,  p.  276,  1852,  not  of 

Ferussac,  1807. 
Sphcerium  occidentale  Prime,  Proc.  Acad.  Nat.  Sci.  Phila.,  for  i860,  p.  295  ; 

Mon.  Am.  Corbie,  p.  41,  fig.  34,  1865. 

Range.  —  Northern  United  States,  Vermont  to  Washington  and 
northward. 

Hell  Gate  River  (Columbia  drainage) ,  Montana ! 
Lower  Saskatchewan  River,  near  Lake  Winnipeg; 
Spokane  Falls,  Wash. 

♦Sphaerium  nobfle  Gould.  Fig. 

Cyclas  nobilis  GovLD,  Proc.  Boston  Soc.  Nat.  Hist.,  v,  p.  229,    S  phariu  m 
1855  ;    San  Pedro,  Cal.  occidentale. 

sphceriutn  nobile  Prime,  Mon.  Am.  Corbie,  p.  41,  fig.  35,  1865. 

Range.  —  California,  Washington,  Idaho. 

Blackfoot  River,  Idaho  !  Seattle,  Wash. 

This  is  not  figured  by  Gould  in  Expedition  Shells,  as  stated  by 
Prime.  It  closely  resembles  S.  dentatum  Hald.,  but  is  less  inflated, 
while  the  young  are  smooth. 


138  LAND    AND    FRESH    WATER    MOLLUSKS 

Sphaerium  patella  Gould. 

Cy das  patella  Gould,   Proc.   Boston  Soc.  Nat.  Hist.,  ill,  p.  292, 
1850;  U.  S.  Expl.  Exped.  Moll.,  p.  426,  pi.  xxxvi,  figs.  527, 
a-b,  1852. 
SJ>hceriufn  patella  Prime,  Mon.  Am,  Corbie,  p,  42,  fig.  36,  1865. 

Fig.  105.       Range.  —  Northern  California  to  British  Columbia. 

SphcEr-       Heal dsburg,  Calif.  !  Wall awalla,  Vancouver  and  Seattle, 

'     77         Wash. ;    Nanaimo,  and  in  duck's   crop  at   Pender  Island ! 

British  Columbia. 

Sphaerium  emarginatum  Prime. 

Cyclas  emarginata  Prime,  Proc.  Boston  Soc.  Nat.  Hist.,  iv,  p.  156,  185 1. 
Sphcerium  emarginatum  Prime,  Mon.  Am.  Corbie,  p.  43,  fig.  38,  1865. 

Range.  —  Lake  Superior ;   Saskatchewan   River  at  Grand  Rapids, 
near  Lake  Winnipeg ! 


106  107 

Fig.  106.     Spkceriuin  emarginatum  Prime. 
Fig.  107.     Sphcerium Jlavum  Prime. 

♦Sphaerium  flavum  Prime. 

Cyclas fiava  Prime,  Proc.  Boston  Soc.  Nat.  Hist.,  iv,  p.  155,  1851. 
Sphcerium  flavum  Prime,  Mon.  Am.  Corbie,  p.  43,  fig.  39,  1865. 

Range.  —  Lake  Superior ;  Sault  Ste.  Marie,  Mich. 

Sphaerium  tumidum  Baird. 

Sphcerium  tumidum  Baird,  Proc.  Zool.  Soc.  London,  1863,  p.  69.  — Prime, 
Mon.  Am.  Corbie,  p.  44,  1865. 

Range.  —  Sumas  Prairie,  Fraser  River  valley,  British  Columbia. 
This  species  appears  not  to  have  been  figured  or  subsequently  recog- 
nized by  collectors. 

Sphaerium  spokani  Baird. 

Sphcerium  spokani  Baird,  Proc.  Zool.  Soc.  London,  for  1863,  p.  69.  —  Prime, 
Mon.  Am.  Corbie,  p.  44,  1865. 

Range.  —  Spokane  and  Kootenai  Rivers,  eastern  British  Columbia. 
Unfigured,  and  not  recognized  by  later  collectors. 

Sphaerium  (Musculium)  raymondi  Cooper. 

Sphcerium  raymondi  J.  G.  Cooper,  Proc.  Acad.  Sci.  Calif.,  2d  series,  iii,  p. 
74,  pi.  I,  figs.  1-8,  1890. 


FAMILY    SPH^RIID^  I39 

Primella  raymondi  Qoov^K,  op.  cit.,  p.  82. 

SphcBriutn  cooperianum  Prime,  Cat.  Corbie,  Am.  Joum.  Conch.,  v,  p.  152, 
1869,  nude  name. 

Range.  —  Alpine  region  of  the  Sierra  Nevada,  Calif.,  to  8,700  feet ; 
Seattle,  Spokane  Falls,  and  Chehalis  River,  Wash. ;  Idaho ;  Vancouver 
Island,  British  Columbia  (Roper). 

Sphaerium  (Musculium)  partumeium  Say. 

Cyclas  partumeia  Say,  Joum.  Acad.  Nat.  Sci.  Phila.,  11,  p.  380,  1822. 
Sphcerium partumeium  Prime,  Mon.  Am.  Corbie,  p.  45,  fig.  42,  1865. 

Range.  —  United  States  from  Nebraska  eastward,  south  to  the  Gulf 
of  Mexico  and  north  to  Manitoba. 

Sphaerium  (Musculium)  jayanum  Prime. 

Cyclas  jayensis  Prime,  Proc.  Boston  Soc.  Nat.  Hist.,  iv,  p.  157,  1851. 
SphcBrium  jayanum  Prime,  Mon.  Am.  Corbie,  p.  46,  fig.  43,  1865. 

Range.  —  Northern  United  States  from  Iowa  eastward,  Canada, 
and  northward. 


Fig.  108.     Sphaerium  jayanum  Prime. 

Lake  Superior ;  Fort  EUice,  Manitoba ;  in  Alberta  at  McLeod, 
Olds,  Crow  Lodge  Creek,  and  Little  Bow  River. 

Sphaerium  (Musculium)  tenue  Prime.     Figure  109. 

Cyclas  tenuis  Prime,  Proc.  Boston  Soc.  Nat.   Hist.,  p.  161,  1851.     Andros- 
coggin River,  Maine. 
Sphcerium  tenue  Prime,  Mon.  Am.  Corbie,  p.  47,  fig.  44,  1865. 

Range.  —  Maine,  Canada,  British  America  and  northern  Alaska. 

Souris  River,  Manitoba ;  Saskatchewan  River  at  Grand  Rapids ; 
Upper  Mackenzie  River  at  old  Fort  Simpson  !  left  bank  of  the  Yukon, 
thirty  miles  below  the  Tanana  River  mouth,  Alaska ! 

Sphaerium  (Musculium)  transversum  Say.    Figure  1 10. 

Cyclas  transversa  Say,  New  Harm.  Disseminator,  11,  p.  356,  1829. 
Sphcerium  transversum  Prime,  Mon.  Am.  Corbie,  p.  48,  fig.  45,  1865. 

Range. — United  States  east  of  the  Rocky  Mountains  and  northward 
to  Canada  and  Manitoba. 


140  LAND   AND    FRESH    WATER   MOLLUSKS 

Stomach  of  sturgeon,  Great  Playgreen  Lake,  Keewatin,  N.  Lat.  54". 


^^y 


109  no  III 

Fig.  109.  Sphceriutn  tenue. 

Fig.  1 10.  SplKBrium  transversum  Say,  with  foot  and  siphons  extended. 

Fig.  HI.  Sphcerium  lenticula. 

Sphaerium  (Musculium)  truncatum  Linsley. 

Cyclas  truncata  Linsley,  Am.  Journ.  Sci.,  vi,  p.  234,  fig.  3,  1848. 
Sphcerium  truncatum  Prime,  Men.  Am.  Corbie,  p.  51,  fig.  50,  1865. 

Range.  —  Eastern  United  States  from  Colorado  to  Maine,  south 
to  the  Ohio  River  and  northward  to  Athabaska. 

Methy  Lake,  Athabaska  (Richardson). 

This  species  is  quite  similar  to  the  European  Cyclas  calyculata^ 
type  of  the  subgenus,  and  was  mistaken  for  it  by  C.  B.  Adams  in  1841. 

Sphaerium  (Musculium)  lenticula  Gould. 

Sphcerium   lenticula    (Gould,   MS.)    Prime,    Proc.  Acad.  Nat.  Sci.   Phila., 

for  i860,  p.  36  (syn.  exclus.). 
Sphcerium   lenticula   (Gould)    Prime,   Mon.  Am.    Corbie,  p.   51,    fig.    51, 

(syn.  exclus.),  1865. 

Range.  —  Carson  and  Klamath  Rivers,  California;  Nanaimo,  Van- 
couver Island,  British  Columbia. 

This  species,  named  in  MS.  by  Dr.  Gould  and  described  by  Prime,  is 
not  the  same  as  the  Lucina  lenticula  Gould,  described  from  Patagonia 
in  the  Mollusca  of  the  Exploring  Expedition.  The  latter,  by  an  en- 
graver's error,  was  called  on  the  plate  (but  not  in  the  text)  Cyclas  len- 
ticula., and  this  seems  to  have  misled  Mr.  Prime,  who  may  not  have 
had  access  to  the  text  of  this  rare  volume. 

*  Sphaerium  stagnicola  J.  de  C.  Sowerby. 

Cyclas  stagnicola  Sowerby,  in  Richardson,  Fauna  Bor.  Am.,  iii,  p.  316, 
1836,  Methy  Lake,  Athabaska. 

♦Sphaerium  medium  J.  de  C.  Sowerby. 

Cyclas  media  Sowerby,  op.  cit.,  Methy  Lake,  Athabaska. 

The  two  names  above  cited  from  Sowerby  are  not  described  in 
Richardson's  work  and  I  am  unable  to  find  any  other  reference  to 
them  in  the  literature.     I  presume  they  are  undescribed. 


FAMILY   SPH^RIID^  I4I 

*  Sphaerium  primeanum  Clessin. 

Spkcerium primeanum  Clessin,  Malak.  Blatt.,  XXV,  p.  122,  pi.  V,  figs.  I,  a-b, 

1878. 

Range.  —  Portland,  Oregon  ;  Seattle,  Wash. 

This  species,  which  has  a  remarkable  resemblance  to  a  Bornia^ 
judging  by  the  figure,  is  not  otherwise  known  to  me,  but,  if  the  local- 
ities given  are  correct,  may  also  extend  to  British  Columbia.  Accord- 
ing to  Roper  it  closely  resembles  S.  rhomhoideum  Say. 

Genus  Comeocyclas  Ferussac. 
(+  Pisidium  C.  Pfeiffer.) 

Comeocyclas  (Phymesoda)  virginica  Gmelin. 

Tellina  virginica  Gmelix,  Syst.  Nat.,  vi,  p.   3236,  1792  ;   based  on  Lister, 

Conch.,  pi.  CLix,  fig,  15,  from  Virginia. 
Cydas  dubia  Say,  Nicholson's  Elncycl.,  ist  Am.  ed.,  pi.  i,  fig.  10,  1817. 
Phymesoda  dubia  (Say)  Rafinesque,  Ann.  Gen.  Sci.  Phys.,  v,  p.  319,  1820. 
Pisidium  virginicum  Bourguignat,  Amen.  Mai.,  i,  p.   53,  1853.  —  Prime, 

Mon.  Am.  Corbie,  p.  61,  figs.  61,  62,  1865. 

Range.  —  United  States,  east  of  the  Rocky  Moun- 
tains, northward  to  British  America  and  Alaska. 

Lake  of  the  Woods  ;  Manitoba ;  Yukon  River,  Alaska, 
thirty  miles  below  the  Xanana  River  mouth !   also  at 
^  ■         *     Nulato !    and  the  Mission !    Lake  Superior,  near  St. 

Comeocyclas  '^  ' 

virginica.  Ignace  Id.,  in  8  to  13  fathoms  (S.  I.  Smith). 

Comeocyclas  (Phymesoda?)  idahoensis  Roper. 
Pisidium  idahoense  Roper,  Nautilus,  iv,  p.  85,  Dec,  1896. 

Range.  —  Old  Mission,  northern  Idaho  (Hemphill)  ;  Seattle,  Wash. 
Stewart  River,  Yukon  District,  Dawson  (^Jide  Sterki). 

Comeocyclas  (Phymesoda)  scutellata  Sterki. 
Pisidium  scutellatum  Sterki,  Nautilus,  x,  p.  66,  Oct.,  1890. 

Range.  —  Lake  Michigan  to  Montana;  Lake  Patten,  Wash.,  Pine 
Lake,  Mich. ;  Orchard  Lake,  Minn. ;  Sheldon,  Montana ;  Frances 
Lake,  Liard  River,  Yukon  District  (^Jide  Sterki),  collected  by  Daw- 
son in  1887. 

Comeocyclas  aequilateralis  Prime. 

Pisidium  aquilaterale  Prime,  Boston  Joum.  Nat.  Hist.,  vi,  p. 
366,  pi.  xii,  figs.  23-25,  1852;  Mon.  Am.  Corbie,  p.  63, 
figs.  65-66,  1865.  Fig.  113. 

Range.  — Maine  to  Michigan,  northward  and  westward  feguilate- 
to  Alaska.  rale  Prime. 


# 


142 


LAND    AND    FRESH    WATER    MOLLUSKS 


Fig.  114.     Corneocyclas 
variabilis  Prime. 


Kotzebue  Sound,  Alaska  !  in  marl  associated  with  mammoth  bones, 
at  Elephant  Point.     Bering  Island,  Bering  Sea  ! 

The  specimens  above  referred  to  were  identified  for  me  by  Mr. 
Prime. 

Corneocyclas  (Cymatocyclas)  compressa  Prime. 

Pisidium  compressum  Prime,  Proc.  Boston  See.  Nat. 
Hist.,  IV,  p.  164,  185 1  ;  Men.  Am.  Corbie,  p. 
64,  figs.  67-68,  1865. 

Range.  —  Maine  to  California  ;  Canada,  the 
Yukon. 

Lake  Superior,  near  Ignace  Id.,  in  4-6 
fathoms ;  White  Pine,  Nevada ;  Sierra  Nevada 
to  9,000  feet  near  Summit,  Calif. ;  Ventura 
Co.,  Calif. ;  Vancouver  Island,  British  Colum- 
bia (Raymond)  ;  Green  Lake,  Seattle,  Wash. ; 
Stewart  River,  Yukon  District  (^fide  Sterki). 

Corneocyclas  variabilis  Prime. 

Pisidium  variabile  Prime,   Proc.   Boston  Soc.  Nat.   Hist.,  iv,  p.    163,  1851  ; 
Men.  Am.  Corbie,  p.  66,  figs.  69,  70,  1865. 

Range.  —  Eastern  United  States,  north  of  Virginia  ;  Colorado,  and 
northward;   Seattle,  Wash. 

Pine  Creek,  Manitoba ;  Stewart  River,  Yukon  District  {^Jide  Sterki) . 

Corneocyclas  abdita  Haldeman. 

Pisidium  abditum  Haldeman,  Proc.  Acad.  Nat.  Sci.  Phila. 
Prime,  Mon.  Am.  Corbie,  p.  68,  figs.  72,  73,  1865. 

Range.  —  North  America,  from  Honduras  northward  to  Alaska. 
Marl    Lake,  Anticosti !    Lake  Superior  in   4  to    13  fathoms  near 
Ignace   Island ;    Manitoba ;    Assiniboia   at   Qu'Appelle !    Alberta,   at 
Laggan,  Red  Deer,  Olds,  McLeod,  Battle   River,  up  to  5,200   feet 
elevation ;  east  slope  of  the  Sierra  Nevada  up  to 
7, 1 00  feet;  in  Colorado  up  to  9,300  feet;  west 
slope  of  the  Sierra  below  5,300  feet  in  Califor- 
nia ;  Seattle,  Wash. ;  in  Alaska  at  Seldovia,  Cook 
Inlet !    Coal  Harbor !    Unga  Island,  Shumagins, 
in   small    pools    on   the    tundra ;    Akun   Island ! 
Aleutians ;    the  Yukon  River,   30   miles   below 
the  mouth  of  the  Tanana !   and  Bering   Island, 


I,  p.  53,  1841.— 


Fig.  115.     Corneocy- 
clas abdita  Hald. 


Bering  Se.- 


This   is  the    most    common   and  widespread   species,  out    of   the 
varieties  of  which  many  nominal  species  have  been  made. 


FAMILY    SPH^RIID^  I43 

♦Coraeocyclas  abyssorum  Stimpson. 

Pisidium  (sp.)  Smith  and  Verrill,  Am.  Journ.  Sci.,  il,  p.  448,  Dec,  1871. 
Pisidium  abyssomus  (Stm.)  Hoy,  Trans.  Wisconsin  Acad.  Sci.,   i,  p.   100, 

1872  (err.  typ.). 
Pisidium  abditum  var.  abyssorum  Stimpson,  S.  I.  Smith  in  Rep.  U.  S.  Fish 

Com.  for  1872-3,  p.  704,  1874. 
Pisidium  abyssorum  Sterki,  Nautilus,  xi,  p.  124,  March,  1898. 

Range.  —  Deep  water  of  the  Great  Lakes,  and  of  the  lake  region 
of  northern  Michigan  and  Minnesota. 

Lake  Michigan;   Lake  Superior  to  a  depth  of    159  fathoms   (food 
of  Coregonus)  ;  Pine  Lake,  Mich. ;  Green  Lake,  Wisconsin. 

This  is  another  of  the  extra-limital  species  which 
search  will  probably  reveal  in  Lake  Winnipeg  and  other 
northern  lakes. 


Comeocyclas  ventricosa  Prime. 

Pisidium  ventricosum  Prime,  Proc.  Boston  Soc.  Nat.  Hist., 

IV,  p.  68,  185 1  ;    Mon.  Am.  Corbie,  p.  72,  figs.  70,   80,  _  - 

1865.  .P    /  .     S     /y.       .  Fig.   1 16. 

Corneocyclas 
Range.  —  Massachusetts,  Canada,  and  northward  to     ventricosa. 

Great  Slave  Lake. 

Comeocyclas  rotundata  Prime. 

Pisidium  rotundatum  Prime,  Proc.  Boston  Soc.  Nat.  Hist.,  iv,  p. 
164,  1 85 1  ;  Mon.  Am.  Corbie,  p.  72,  figs.  81,  82,  1865. 

Range. — Lake  Superior  region;  Manitoba;  St.  Paul  Fig.  117. 
Island,  Bering  Sea  !  Comeocy 

Comeocyclas  steenbuchii  Moller.  \  °l  / ''' 

•'  tunaata. 

Cy c las  steenbuchii  MouL.^K,  Index  Moll.  Gronl.,  p.  20,  1842. 
Pisidium  steenbuchii  MoRCH,  Am.  Journ.  Conch.,  iv,  p.  37,   1868;   ibid., 
Rink's  Greenland,  App.,  p.  440,  1877. 

Range.  —  Greenland,  on  the  west  coast!  Iceland!  Ungava,  Lab- 
rador. 

This  species  appears  to  be  unfigured,  but  there  are  specimens  in 
the  Jeffreys  collection  from  Iceland  as  well  as  Greenland.  It  appears 
to  belong  to  the  section  Cyclocalyx. 

Corneocyclas  occidentalis  Newcomb. 

Pisidium  occidentale  Newcomb,   Proc.  Calif.  Acad.  Sci.,  ll,  p.  94,  1863. — 
Prime,  Mon.  Am.  Corbie,  p.  73,  1865. 

Range. — California  to  British  Columbia. 

East  slope  of  Sierra  Nevada,  in  California,  to"9,7oo  feet.  Nanaimo, 
Vancouver  Island,  British  Columbia ;  Spokane  Falls,  Wash. 


144 


LAND   AND    FRESH   WATER   MOLLUSKS 


Fig.  iii 


This  unfigured  species  has  been  regarded  by  Roper  as  only  a  muta- 
tion of  C.  abdita  Haldeman. 

Comeocyclas  ultramontana  Prime. 

Pisidium  ultramontanum  Prime,  Mon.  Am.  Corbie,  p.  75, 
fig.  85,  1865. 

Range.  —  Canoe  Creek,  California  ;  Seattle,  Wash. ; 

Nanaimo,  Vancouver  Island,  and  Pender  Island  !  British 
/",   ,        1  .  Corneocyclas 

Columbia.  ,^       •'  ^ 

ultramonta- 

Comeocyclas  arctica  Westerlund.  na  Prime. 

Pisidium  arcticum  Westerlund,  Vega  Exp.  Vetens.  lakt.,  iv,  p.  217,  1885. 
Range.  —  Port  Clarence,  Alaska. 

Corneocyclas  nivalis  Westerlund. 
Pisidium  nivale  Westerlund,  op.  cit.,  p.  218,  1885. 
Range.  —  Port  Clarence,  Alaska. 

Corneocyclas  glacialis  Westerlund. 
Pisidium  glacialeV^-EST^^i^v^D,  op.  cit.,  p.  218,  1885. 
Range.  —  Port  Clarence,  Alaska. 

*  Corneocyclas  sibirica  Clessin. 

Pisidium  sibiricum  Clessin,  K.  Svenska  Vet.  Ak.  Forh.,  p.  70,  fig.  23,  1877  ; 
Mon.  Pisidium,  Conch.  Cab.,  ed.  11,  pi.  vii,figs.  15-17,  1877. — Wester- 
lund, Fauna  Pal.  Reg.,  vii,  p.  23,  1890. 

Range. — Western  Siberia,  on  the  Yenisei  River  to  60°  50'  N.  Lat., 
>  Port  Clarence,  Alaska. 

*  Corneocyclas  borealis  Clessin. 

Pisidium  boreale  Clessin,  in  Westerlund,  Fauna  Pal.  Reg.,  vii,  p.  32,  1890. 

Range.  —  Western  Siberia  at  Lusino.      .''Port  Clarence,  Alaska. 

The  preceding  five  species  are  ascribed  to  Port  Clarence  on  the 
authority  of  the  literature  solely.  I  have  not  seen  specimens  of  any 
of  them.  I  suspect  that  the  C.  sibirica  and  borealis  reappear  in  the 
form  of  new  species,  among  the  three  nominal  species  preceding  them. 

Corneocyclas  pulchella  Jenyns. 

Cydas  pulchella  Jenyns,  Trans.  Phil.  See.  Cambridge,  1832,  p.  306,  pi.  x, 
figs.,  1812;  not  of  Deshayes,  1835,  nor  Gassies,  1849. — Sowerbv,  in 
Richardson,  Fauna  Bor.  Am.,  iii,  p.  316,  1836. 

Range.  —  Middle  and  Northern  Europe  to  69°  N.  Lat.     Arctic 

America  ? 

Methy  Lake,  Athabaska  (Richardson). 


FAMILY    SPH^RIID^  I45 

*  Corneocyclas  randolphi  Roper. 

Pisidium  randolphi  Roper,  Nautilus,  ix,  p.  99,  Dec,  1895. 

Range. —  Seattle,  Washington. 

This  species  is  finely  striated,  very  much  like  C.  abdita  in  general 
form,  but  of  a  peculiar  and  unique  greenish-yellow  color.  It  may 
very  likely  extend  into  British  Columbia. 

Corneocyclas  (Tropidocyclas)  henslowana  Sheppard. 

Tellina  henslowana  Sheppard,  Trans.  Linn.  Soc,  xiv,  p.  150,  1825. 
Cyclas  appendiculata  (Leach  MS.)  Turton,  Man.,  ed.  i,  p.  15,  pi.  xv,  fig. 
6,  1831. — SowERBY,  in  Richardson,  Fauna  Bor.  Am.,  in,  p.  316,  1836. 
Pisidium  henslowianum  Jenyns,  Mon.  Cyclas,  p.  20,  pi.  xxi,  figs.  6,  7,  1832. 

Range.  —  Europe  north  of  the  Alps  ;   Canada  ;  British  America. 

Hamilton  Bay,  Lake  Ontario ;  Lake  Superior  to  Lake  Winnipeg 
(Richardson). 

The  record  from  Richardson  was  naturally  thought  to  be  a  misiden- 
tification,  but  the  recent  discovery  in  Lake  Ontario  of  undoubted  speci- 
mens of  this  species,  leads  to  the  belief  that  Sowerby,  who  certainly 
should  have  known  a  common  British  species,  may  after  all  have  been 
correct. 

In  closing  the  list  of  Sphceriidce  I  may  be  allowed  to  observe  that 
so  large  a  part  of  it  is  derived  from  the  literature,  and  not  from  the 
present  examination  of  specimens,  that  I  do  not  feel  the  confidence  in 
the  validity  of  all  the  species,  or  the  correctness  of  all  the  identifica- 
tions that  I  might  have  felt  under  other  circumstances.  Until  the  very 
numerous  species  which  have  been  named  among  American  Pisidia  of 
late  years,  shall  have  been  adequately  illustrated  and  some  knowledge 
gained  of  the  range  of  variation  in  these  minute  forms,  a  healthy  skep- 
ticism in  regard  to  our  population  of  this  genus  will  doubtless  continue 
to  prevail  among  collectors  of  fresh  water  shells. 


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19-22,  1853. 
Martens,  Carl  Eduard  von. 

1855     Ueber  der  Verbreitung  der  Europaeischen  Land-  und  Siisswasser-Gaster- 

opoden.     Inaugural  dissertation,  Tubingen,  1855,  pp.  144,  8°. 
1872     Conchjlien  aus  Alaschka.     Malakozoologische  Blatter,  xix,  pp.  78-80. 

1872. 
i88a     [Shells  of  the  Krause  Expedition.]     Sitzungsbericht  der  Ges.  Naturf 
Freunde  zu  Berlin,  1882,  No.  9,  pp.  138-143. 

1885  Binnen  Mollusken  aus  Mittel-  und  Ost-Asien.     Conchol.  Mittheil.,  11, 
heft  v,  pp.  179-185,  1885. 

Mayer,  Charles. 

1869     [Mollusca  of  the   Plant  beds]   Heer,  Flora  fossilis  Alaskana  ;    Kong. 

Svensk.  Vetensk.-Akad.  Handl.,  n.  ser. ,  viii,  pp.  40-41,  pi.  x,  figs.  7-13, 

1869. 
Middendorff,  A.  Th.  von. 

1851     Sibirische  Reise.     Siisswasser  und  Land  Mollusken,  11,  Th.  i,  pp.  273- 

308,  389-433,  1851. 
1851     Beschreibung  einen  neuen  Molluskenarten,  nebst  einem  Blicke  auf  den 

geographischen  Charakter  den  Land-  und  Siisswasser-Mollusken  Nord 

Asiens.     Bull.  Phys.  Math.  Akad.  Imp.  des  Sci.  St.  Petersburg,  ix,  pp. 

108-112,  1851.    Melanges  Biol.,  i,  pp.  160-164,  1851.     See  also  Maack,  R. 

HSUer,  H.  P.  C. 

1842     Index  MoUuscorum  Groenlandiae.     Hafnise,  C.  A.  Reitzel,   1842,  8°, 
pp.  26. 


BIBLIOGRAPHY  I5I 

Morch,  0.  A.  L. 

1868  On  the  Land  and  Fresh  Water  Mollusca  of  Greenland.  Amer.  Jour. 
Conch.,  IV,  pp.  25-40,  pis.  Ill,  IV,  i868. 

1857  Prodromus  Fauna  MoUuscorum  Gronlandiae.  Rink's  Greenland,  App., 
pp.  75-100,  1857.  A  second  edition,  revised  and  augmented,  in  the 
Arctic  Manual,  London,  1875,  pp.  124-135. 

1877  The  Greenland  Fauna,  iv,  Mollusca.  Rink's  Danish  Greenland,  Lon- 
don, 1877,  Appendix,  pp.  435-442. 

Morelet,  Arthur. 

1858  Coquilles  Terrestres  du  Kamtchatka.  Journal  da  Conchyliologie,  vii 
Juillet,  1858,  pp.  7-9. 

Mousson,  Albert. 

1887  Coquilles  Terrestres  et  Fluviatiles  recueillies  par  M.  Louis  Graeser  dans 
le  bassin  de  1' Amour  (etc.).  Journal de Conchjl.,  xxxv,  pp.  10-32,  Jan., 
1887. 

Note. — This  paper  was  only  discovered  after  the  completion  of  the 
present  memoir.  Nearly  all  the  species  mentioned  in  it  are  from  the 
upper  waters  of  the  Amur  River,  or  from  Vladivostok.  Succinea  insu- 
laris  Mousson,  from  an  island  at  the  mouth  of  the  Amur,  is  the  only 
addition  to  the  species  properly  belonging  to  the  Primorski  province, 
treated  of  in  my  discussion  of  the  species  of  the  Northeast  coast  of 
Siberia,  but  several  are  added  to  the  list  of  Mongolian  elements  of  the 
fauna  of  the  Amur  drainage. 

Nylander,  Olof  0. 

1899    A  list  of  Shells  from  Northeastern  Maine.     The  Nautilus,  xiii,  No.  8, 

Dec,  1899,  pp.  102-106. 
190X     Distribution    of  Limncea   emarginata  Say,   and  the   variety  Mighelsii 
Binney,  in   Fish  River,  Aroostook  Co.,  Maine.     8°,  pp.   1-4,  pi.  i-xv, 
Caribou,  Maine,  the  author,  1901. 

Pilsbry,  H.  A. 

t888  Lyogyrus,  Gill,  and  other  American  Shells.  Conchologist's  Exchange, 
II,  p.  113,  1888. 

1898  Descriptions  of  new  species  and  varieties  of  American  Zonitidae  and 
Endodontidse.     The  Nautilus,  xii,  No.  8,  Dec,  1898,  pp.  85-87. 

1899  New  and  little  known  species  of  Pristiloma.  Proc  Acad.  Nat.  Sciences, 
Philadelphia,  for  1899,  pp.  185-187,  pi.  ix. 

1899     Remarks  on  the  American  species  of  Conulus.     The  Nautilus,  xii,  No. 

10,  Feb.,  1899,  pp.  113-117. 
1899    Notes  on  a  few  Northwest   American  Land  Snails.     Proc.  Acad.  Nat. 

Sciences,  Philadelphia,  for  1899,  pp.  314-315. 

Poirier,  Pascal. 

1883     Report  of  the  Conchological    Branch  (for  1882).     Transactions  Ot- 
tawa Field  Naturalist's  Club,  i,  No.  4,  1883,  p.  74. 
Posselt,  Henrik  J. 

1898  Conspectus  Fauna  Gronlandicse.  Meddelelser  om  Gr5nland,  xxiii,  pp. 
XX,  298,  2  pi.  and  i  map.  8°.  Kjobenhavn,  Bianco  Luno,  1898;  cf.  pp. 
257-268. 


152  LAND    AND    FRESH   WATER    MOLLUSKS 

ProTancher,  L6on. 

i8go     Les  Mollusques  de  la  Province  de  Quebec.     Le  Naturaliste  Canadien, 
XXIII,  No.  9,  Mar.,  1890,  pp.  184-187,  and  No.  10,  April,  pp.  203-205. 
Rackett,  Thomas. 

X822    Descriptions  of   some  Shells  found  in  Canada.     Transactions  Linnean 
Soc,  XIII,  pp.  42-43,  1822. 
Randolph,  P.  B. 

1899     Collecting  Shells  in  the  Klondike  country.     The  Nautilus,  xii,  No.  10, 
Feb.,  1899,  pp.  109-112. 
Reinhart,  J. 

1883     Die  von  den  Herren  Gebriider  Krause  auf  ihrer  Reise  gesammeltea 
Pupa-,  Hyalina-,  und  Vallonia-a.rten.     Sitzungsbericht  der  Ges.  Naturf . 
Freunde  zu  Berlin,  1883,  No.  3,  pp.  37-43. 
Schrenck,  Leopold  von. 

1867  Reisen  und  Forschungen  im  Amurlande  in  den  jahren  1854-1856.  II, 
(3)  :  MoUusken  des  Amurlandes  und  des  Nordjapanisches  Meeres.  St. 
Petersburg,  K.  Akad.  der  Wissenchaften,  1867,  4°,  pp.  259-976. 

Sheppard,  Mrs.,  of  Woodfield 

1829     On   the   Recent   Shells   which   characterize  Quebec  and  its  environs. 
Trans.  Literary  and  Scientific  Society  of  Quebec  for  1829,  i,  pp.  188-198. 
Shimek,  B. 

1893     List  of  the  Shells  collected  on  the  Lower  Saskatchewan  in  1892  by  C.  C. 
Nutting.     Bulletin  University  of  Iowa,  Nat  Hist.,  11,  1893,  pp.  291-292. 
Cf.  also  Ottawa  Naturalist,  x,  p.  15,  1896. 
Siemaschko,  Julian  Marc  von. 

1849     Bemerkungen    ueber   einige   Land-  und   Susswasser-MoUusken    Russ- 
lands.     Bull.  Phys.  Math.  Akad.  Imp.  des  Sci.  de  St.  P^tersbourg,  vii, 
1848,  pp.  225-240,  1849. 
Small,  H.  B.,  and  Symes  P.  B. 

1882     Report  of  the  Conchological  Branch  (for  1881).     Transactions  Ottawa 
Field  Naturalist's  Club,  i,  No.  3,  1882,  pp.  57-59. 
Sowerby,  James  de  Carle. 

1836     Mollusca.     Richardson,  Fauna  Boreali-Americana,  iii,  p.  315,  London, 
1836. 
Taylor,  George  W. 

1889    The  Land  Shells  of  Vancouver  Island.     Ottawa  Naturalist,  lu,  No.  3, 

pp.  84-94,  1889. 
1891     Land  Shells  of  Vancouver  Island.     The  Nautilus,  v.  No.  8,  Dec,  1891, 

pp.  91-92. 
1893    Land  and  Freshwater  Shells  in  the  Rocky  Mountains.     The  Nautilus, 

VII,  No.  8,  Dec,  1893,  p.  85. 
X895     The  Land  and  Freshwater  Shells  of  Alberta.     Ottawa  Naturalist,  ix,  No. 

9,  Dec,  1895,  pp.  173-178. 
X897    Planorbis  nautileus  in  America.     The  Nautilus,  x.  No.  12,  pp.  139-140, 
April,  1897. 
Taylor,  John  W. 
1885    Description  of  a  New  Species  of  Planorbis  from  Manitoba.    Journal  of 
Conchology,  iv  (Leeds),  1885,  p.  351. 


BIBLIOGRAPHY  153 

Tryon,  George  W. 

1865    Descriptions  of  New  Species  of  North  American  Limnaeidse.    Amer. 
Joum.  Conch.,  i,  p.  231,  1865. 
Vanatta,  E.  6. 

i8g6    The  Geographic  Distribution  of  Planorbis  umbilicatellus.    The  Nautilus, 
IX,  No.  10,  Feb.,  1896,  p.  117. 
Westerlond,  Carl  Agardh. 

1883  Von  der  Vega  Exp.  in  Asien  gesammelten  Binnen  Mollusken.  Nach- 
richtsbl.  d.  Deutschen  Malak.  Gas.,  xv,  pp.  48-59,  April,  1883. 

1885     Land  och   Sotvatter   Mollusker,   insamlade  under   Vega-expeditionen. 
Vega  Exped.  Vetenskapliga  lakttagelser,  iv,  pp.  141-220,  1885. 
Whiteaves,  J.  F. 

X863  On  the  Land  and  Freshwater  Mollusca  of  Lower  Canada.  Canadian 
Naturalist,  Feb.,  1863,  pp.  50-65.  April,  pp.  98-107.  Extra  copies  pp. 
1-3 1,  1863. 

1880  List  of  Freshwater  Mollusca  from  Manitoba  and  the  valley  of  the  Nelson 
River.  Geological  Survey  of  Canada,  Report  of  Progress  for  1878-79, 
Montreal,  1880.  Report  of  Explorations  of  the  Churchill  and  Nelson 
Rivers,  hy  Robert  Bell.     Appendix,  iii,  pp.  61-62,  c. 

z88i  Mollusca.  Geological  Survey  of  Canada.  Report  of  Progress  for  1879- 
80,  Montreal,  1881.  Report  on  Hudson's  Bay,  by  Robert  Bell.  Ap- 
pendix, IV,  pp.  75-76,  c. 

1887  On  some  Marine  Invertebrata  dredged,  or  otherwise  collected,  by  Dr. 
G.  M.  Dawson,  in  1S85,  on  the  coast  of  British  Columbia,  with  a  sup- 
plementary list  of  a  few  Land  and  Fresh  Water  Shells  (etc)  from  the  same 
region.  Transactions  Royal  Society  of  Canada  for  1886,  iv,  section  iv, 
1887,  pp.  IH-137,  with  4  text-figures. 

1895  Notes  on  Recent  Canadian  Unionids.  Canadian  Record  of  Science, 
VI,  No.  5,  Jan.,  1895,  pp.  250-263. 

1895  Additional  notes  on  Recent  Canadian  Unionidae.  Canadian  Record  of 
Science,  vi,  No.  5,  Jan.,  1895,  pp.  365-366. 

1895  Recent  Mollusca  from  the  headwaters  of  the  Ottawa.  Ottawa  Natural- 
ist, IX,  April,  1895,  p.  22. 

Z90Z  Notes  on  some  Land  and  Freshwater  Mollusca  from  Fort  Chimo,  Ungava 
Bay,  Ungava.    Ottawa  Naturalist,  xiv,  No.  12,  Mar.,  1901,  pp.  221-223. 

igoa  Notes  on  some  Fresh  Water  and  Land  Shells  from  Keewatin,  Northern 
Ontario  and  British  Columbia.     Ottawa  Naturalist,  xvi,  1902,  pp.  91-92. 

1905  Notes  on  some  Freshwater  Shells  from  the  Yukon  Territory.  Nauti- 
lus, XIX,  No.  I,  pp.  1-3,  May,  1905. 

X905  Lists  of  a  few  species  of  Land  and  Freshwater  Shells  from  the  immedi- 
ate vicinity  of  James  Bay,  Hudson  Bay.  Nautilus,  xix.  No.  i,  p.  4, 
May,  1905. 


PLATE  I. 

(The  figures  are  natural  size.) 

Fig.  I.  Lytnncea  freblei  Dall.    The  reflected  margin  of  the  aperture  below 
the  umbilicus  is  somewhat  broken.     See  p.  70. 

2.  A  younger  specimen  of  the  same  species  from  behind. 

3.  LymncBa  randolfhi  F.  C.  Baker;  p.  71. 

4.  The  same  species,  another  specimen,  from  behind  ;  p.  71.' 

(154) 


H.  A.   E.  VOL.  Xill 


FRESHWATER  SHELLS  OF  ALASKA 


HELIOTYPE   CO.,    BOSTON. 


PLATE  II. 

(The  specimens  are  figured  natural  size  except  when  otherwise  stated.) 

Figs.  1,2.        Fa/r;a/a  Ac//c«Vfea  Dall,  magnified  four  diameters.     The  umbilicus 
is  partly  hidden  by  a  calcareous  deposit ;  p.  123. 

3.  Lymncea  fetersi  Dall ;  p.  66. 

4,  5.       Lymncea  anticostiana  Dall;  p.  79. 

6.  Lymncea  ?  ferpolita  Dall ;  p.  78. 

7.  9.       Lymncea  atkaensis  Dall ;  p.  66. 

8.  Lymncea  ?  perpolita  Dall,  magnified  two  diameters ;  p.  78. 
10,  11.  Planorbula  ckrisiyi  Dall,  magnified  two  diameters  ;  p.  99. 

(156) 


H.  A.  E.  VOL.  XIII 


□ 


FRESHWATER  SHELLS  OF  ALASKA 


HELIOTYPE    CO.,    BOSTON. 


tBTARr 

OF  THE 


INDEX   TO   GENERA  AND    SPECIES 


New  genera  and  species  and  the  pages  on  which  they  are  described  are  in 
black-face  type ;  synonyms  in  parenthesis  ;  pages  where  synonymy  of  known 
species  or  genera  is  given  in  italics;  varietal  names  are  treated  as  specific  for 
the  purposes  of  the  Index. 


Acanthinula  21 

aculeata  21 

harpa  (22) 
Acella  (60),  64,  72 

kirtlandiana  72 
Achatinidae  33 
Acmsea  113 
Acroloxus  108,  109 
Acroxus  (108) 
Adelina  (60) 

elegans  60 
Adula  (82) 
Agriolimax  ^5 

agrestis  4^ 

berendti  46 

campestris  46 

hyperboreus  4^ 
Alasmidonta  costata  (131 
Alasmodon  falcata  (132) 

rhombica  (127) 

yubaensis  (132) 
Alasmodonta  arcuata  (132) 

complanata  (131) 

dahurica  (132) 

rugosa  (131) 
Amalia  46 

gagates  46 

hewstoni  46 
Ameria  lOI 
Amnicola  /// 

cincinnatiensis  118 

emarginata  118 

granum  (118) 

hindsii  (119) 

lapidaria  (119) 

limosa  iij 

pallida  /// 

porata  (117) 


Amnicolidx  7/7 
Amphibinajj 

avara  55 

pfeifferi  55 
Amphibulima  (55) 

cuculata  55 

patula  55 
Amphibulimus  (55) 
Amphibulina  (55) 
Amphipeplea  78 
Amplexa  (104) 
Amplexis  (22) 
Amplexus  (22),  (104) 
Ancaeus  (82) 
Ancylastrum  108,  109 

cumingianus  108 
Ancyllus  (108) 
Ancylus  11,  107,  (108),  109 

caurinus  (no) 

cumingianus  108,  109 

fluviatilis  107,  108,  109 

fragilis  no 

fuscus  109 

kootaniensis  1 10 

lacustris  107,  108,  I09 

newberryi  109 

parallelus  no 

patelloides  109 

radiatus  108 

rivularis  log,  (no) 
Anguispira  alternata  (49) 

bruneri  (52) 
Angustula  milium  (32) 
Anisopsis  (81),  85 
Anisus  81,  (82),  84 
Anodon  areolatus  (127) 

biangulata  (130) 

exilis  (129) 


(157) 


158 


INDEX 


Anodon  feminalis  (130) 

rostratus  (128) 

rugosus  (127) 

triangularis  (128) 
Anodonta  I2j 

angulata  (130) 

argentea  (131) 

arkansasensis  (127) 

beringiana  10,  I2J 

biangulata  (130) 

buchanensis  (131) 

ccllensis  (127) 

cognata  (128) 

dallasiana  (130) 

denigrata  (131) 

edentula  ( 127) 

feminalis  (130) 

ferruginea  (131) 

ferussaciana  (130) 

flava  (129) 

footiana  (129),  129 

fragilis  (129) 

gigantea  (X29) 

glandulosa  (129) 

grandis  I2g 

housatonica  (129) 

implicata  i2g 

irisans  (129) 

kennerleji  128 

kennicotti  130 

lacustris  (129) 

laosensis  (128) 

lewisii  (129) 

marginata  128 

marryattiana  (129) 

modesta  (131) 

newtonensis  (129) 

nuttalliana  128 

oblita  (131) 

oregonensis  128 

ovata  (129) 

pallida  (129) 

pavonia  (127) 

pepiniana  130 

plicata  (131) 

randalli  (130) 

rotundata  (128) 

rotundovata  (128) 

salmonea  (127),  (129) 


Anodonta  shaefferiana  (127) 

showalteri  (127) 

Simpson iana  (130) 

subcarinata  (129) 

subcylindracea  (131) 

tetragon  a  (127) 

triangularis  (128) 

undulata  (127) 

wahlamatensis  128 

wardiana  (127) 

youconensis  (127) 

joukanensis  (127) 
Anodontoides  130 

ferussacianus  130 
AnsuIuE  (108) 
Ansylus  (108) 
Aplecta  (104),  106 
Aplexa  100,  102,  104,  105,  107 

hordacea  103 

hypnorum  12,  104,  105,  106,  I07 
Aplexus  (104) 

hypnorum  107 
Aictonchis  112 

borealis  112 
Arianta  arbustorum  21 
Ariolimax  34,  35,  47 

columbianus  ^t/,  48 

maculatus  48 

steindachneri  48 

stramineus  48 
Arion  andersoni  (46) 

foliolatus  (47) 
Arionidae  46 

Arionta  ptychophora  (25) 
Armiger  5j,  86 

crista  96 
Arnouldia  (40) 

fulva  (41) 
Aulaca  (21) 
Auricella  (115) 
Auricula  (115) 
Auricularia  (60) 
Auriculidx  //j 
Auriculina  (115) 

Bathyomphalus  <?J,  86 
Bifidaria  27 

armifera  2J 

contracta  27 


INDEX 


159 


Bifidaria  holzingeri  28 

pentodon  28 
Bornia  141 
Brachyspira  (55) 
Brondelia  109 

drouetiana  109 
Buccinum  palustre  62,  (76) 

truncatulum  62,  (72) 
Buliminus  obscurus  41 
Bulimnea  (60),  63 

megasoma  67,  70 
Bulimulus  pilula  79 
Bulimus  (104),  105,  (115) 

harpa  (21) 

hypnorum  (106) 

lubricoides  (33) 
Bulinus  (100),  (loi),  (104),  105,  107 

hordaceus  (104) 

hvpnorum  107 

per  la  105 

pictus  107 

senegalensis  105 

turritus  105 
Bulla  (104) 

fontinalis  99,  100 

hypnorum  104,  105,  (106) 

turrita  (106) 
Bullinus  (100),  (104) 

fontinalis  100 

turritus  (106) 
Bjthinella  obtusa  118 
Bythinia  105 

Caillaudia  (81) 

angulata  81 
Campeloma  124 

decisum  124,  125 
Carinifex  63 
Carychium  7/5,  116 

exiguum  115,  116 

exile  1/6 

minimum  115 
Cepaea  hortensis  (20) 
Chilostoma  (22) 
Chlamydea  36 
Choanomphalus  62 
Cincinna  (120) 

Cincinnatia  cincinnatiensis  IlS 
Cionella  lubrica  (33) 


Circinaria  (22),  33 

cbocolata  34 

hemphilli  35 

hybrida  J5 

sportella  34, 35 

vancouverensis  25,  34,  (35) 

voyana  35 
Circinariidae  33 
Cobresia  (35),  121 
Cochlicopa  jj 

lubrica  jj 
Cochlohydra  (55) 
Complanaria  gigas  (131) 
Concinna  (120) 
Conulus  (39) 

alaskensis  41 

arcticus  (45) 

chersinus  (41) 

fulvus  (40),  (41) 

trochiformis  {41) 
Coretus  (80),  (81),  83 
Corneocyclas  3,  134,  141 

abdita  142,  143,  145 

abyssorum  14J 

aequilateralis  141 

arctica  144 

borealis  144 

compressa  142 

glacialig  144 

henslowana  14J 

idahoensis  141 

nivalis  144 

occidentalis  143 

pulchella  144 

randolphi  144 

rotundata  143 

scute  I  lata  141 

sibirica  144 

steenbuchii  14J 

ultramontana  144 

variabilis  142 

ventricosa  143 

virginica  14T 
Cornu  (81) 
Costatella  (100),  loi 
Costella  (100) 
Cumingia  (108) 
Cyclas  appendiculata  (145) 

aurea  (135) 


i6o 


INDEX 


Cyclas  bulbosa  136 

calyculata  140 

dentata  (137) 

dubia  (141) 

elegans  (136) 

emarginata  (138) 

fabalis  (137) 

flava  (138) 

fuscata  136 

jayensis  (139) 

lenticula  140 

media  (140) 

nobilis  (137) 

ovalis  (137) 

partumeia  (139) 

patella  (138) 

pulchella  (144) 

rhomboida  (136) 

saratogea  (135) 

similis  (134) 

solidula  (136) 

stagnlcola  (140) 

staminea  (136) 

steenbuchii  (143) 

striatina  (135) 

sulcata  (134) 

tenuis  139 

transversa  ( 139) 

truncata  (140) 
Cjclocalyx  143 
Cyclolimnaea  64 
Cyclostoma  lapidaria  (119) 

tricarinata  (121) 
Cymatocyclas  compressa  142 

Dentati  97 
Dentatus  (97) 
Diastropha  (99) 
contorta  100 
Diplodiscus  (82),  85,  86 
Discoidina  (83) 
Discus  (97) 
Drepanotrema  82,  86 

Endodontidse  49 
Enydra  (99) 
Epiphragmophora  21 

fidelis  21 
Erinna  (61),  62,  65 


Erinna  newcombi  61,  65 
Euconulus  jp,  40,  45 

fabricii  41,  42 

fulva  42 

fulvus  39,  (40),  (41) 

trochiformis  40,  41,  42 
Euhadra  iiscina  11 
Eulimneus  (61) 
Eulota  fiscina  11 

flexibilis  II 

weyrichi  il 

Ferrissia  109 

parallelus  no 

rivularis  no 
Ferussacia  subcylindrica  (33) 
Fluminicola//p 

nuttalliana  iig 

virens  iig 
Fossaria  (61) 

Galba  (60),  62,  64 

desidiosa  73 

galbana  73 

holboUi  74 

humilis  73 

truncatula  72 

vahlii  74 
Gallandia  (36) 
Gastrodonta  ^j 

gularis  43 
Giraulus  (83) 
Glaphjra  (22) 
Gljptophysa  loi 
Gonidea  /jo 

angulata  ijo 
Goniobasis  116,  117 

plicifera  116,  117 

silicula  116,  117 
Gonyodiscus  ^o 

striatella  (50) 
Gulnaria  (60) 
Gundlachia  108,  109 

ancyliformis  108 
Gyraulus  5j,  86 

deflectus  94 

hirsutus  93 
Gyrorbis  (82),  85,  (l20) 
Gjrulus  (83) 


INDEX 


i6i 


Haldemania  (lo8) 
Haldenumiiui  97,  98 
Helicidse  3,  19,  20 
Helicodiscus  52 
lineatus  §2 
Helicogona  subpersonata  II 
Helicoliraax  (35),  (36) 
Helisiga  (55) 

sanctsehelense  55 
Helisigna  (55) 
Hellsoma  8j,  84,  85 

bicarinatus  87 
Helix  20,  (39),  (59),  (115) 

albolabris  (26) 

alternata  (49) 

amarula  59 

amurensis  (21) 

arborea  (42) 

arboreus  (42) 

arbustorum  (21) 

asiatica  (23) 

asteriscus  (51) 

attenuata  54 

auricularia  (60) 

baskervillei  (24) 

belcheri  54 

bidentata  41 

breweri  (42) 

chersina  (41),  42 

Columbiana  (24) 

conspecta  (53) 

cooperi  52 

cornea  80,  8l 

corneus  80 

costata  (23) 

crenella  (23) 

cronkhitei  (50) 

devia  (24) 

dubia  (49) 

egena  (41),  42 

electrina  (38) 

engonata  (87) 

fabricii  (41) 

fidelis  (21) 

floccata  51 

fulva  (40) 

germana  (25) 

gularis  (43),  44 

hammonis  (38),  42 


.Helix  harpa  (21) 
hajdeni  (52) 
bortensis  20 
indentata  (39) 
labiosa  (24) 
labyrinthica  (27) 
limitaris  (49) 
lineata  (52) 
lubrica  (33) 
lucida  (42) 
mandralisci  (40) 
milium  (43) 
minuscula  (43) 
minuta  (22) 
minutissima  (53) 
monodon  (26) 
morsel  (39) 
mortoni  (40) 
nitida  41,  (42) 
nitidula  (39),  (40) 
nuttalliana  (21) 
paludosa  (22) 
pellucida  35,  (36) 
planorbis  (80),  81 
ptychophora  (25) 
pulchella  (22),  (23) 
putris  55 
pygmaea  (53) 
radiatula  (38) 
rudis  54' 
solitaria  (49) 
spirorbis  83 
sportella  (35) 

stagnalis  59,  (60),  (62),  (65) 
striatella  (50) 
strigosa  (51) 
subglobosa  (20) 
town  sen  diana  (25) 
trochiformis  (40) 
trochilus  (40) 
trochulus  (40),  41 
vancouverensis  (34) 
velHcata  (34) 
virgata  52 
Hemithalamus  (97) 

nitidus  97 
Hemphillia  48 
camelus  48 
glandulosa  48 


l62 


INDEX 


Heterodiscus  (Si),  Sj 
Hippeutes  (82) 
Hippeutis  82,  86,  (97) 
Hjalina  (35),  (39) 

arborea  (42) 

arctica  (45) 

binnejana  (39) 

binneyi  (39) 

£ulva(4o),  (41) 

indentata  (39) 

nitida  (42) 

pellucida  (38) 

viridula  (38) 
Hyalinia  (39) 

fulva  (40) 

trochiformis  (41) 

lelskia  (120) 
Isidora  loo,  loi,  105 

wahlbergi  loi 
Isthmia  ventricosa  (31) 

pjgmaea  33 

Jelskia  (120),  121 

Laevapex  109 

fragilis  1 10 

kootaniensis  no 
Lampsilis  725 

alatus  126,  127 

borealis  126 

ellipsiformis  126 

gracilis  127 

ligamentinus  /^6 

luteolus  7^5 

radiatus  126 

rectus  126 

superiorensis  125 

ventricosus  /2J 
Lantzia.     See  Erinna. 
Lanx  109 
Lasmigona  131 
Leachia  (60) 

stagnalis  60 
Legrandia  (108) 
Le  Liri  iii 

Leptolimnaea  glaber  64 
Leptolimnea  (60),  62,  64 

elongata  60 


Leptolimnea  glaber  60 
Leptolimneus  (6l) 

glaber  61 
Limacidae  45 
Limacina  (35) 
Limax  agrestis  (45) 

berendti  46 

columbianus  (47) 

hemphilli  46 

hewstoni  (46) 

hjperborea  (45) 
Limnaea  (60),  (61),  62,  (iQS) 

ampla  (68),  (69) 

angulata  (68) 

arctica  (75) 

binneji  (69) 

bulimoides  (79) 

canadensis  (69) 

decisa  (125) 

decoUata  (68) 

elodes  (76) 

elongata  (75) 

emarginata  (69) 

exilis  (72),  77 

ferruginea  (72) 

glabra  61 

gronlandica  (75) 

hajdeni  (76) 

holbolli  (74) 

kingi  61 

kirtlandiana  (72) 

lanceata  (72) 

leucostoma  (75) 

megalosoma  (67) 

megastoma  (67) 

mighelsi  (68) 

minor  (75) 

molleri  (75) 

nuttal liana  C76) 

philadelphica  (74) 

plebeia  (76) 

proxima  (76) 

scalar  is  (69) 

senegalensis  (75) 

stagnalis  (65) 

traski  (74) 

umbilicata  (79) 

vahlii  (74) 

velutina  61,  65 


INDEX 


163 


Limnseus  decollatus  (68) 

elodes  (76) 

elongatus  (77) 
Limnea  (60) 

adelinae  (78) 

caperata  (79) 

catascopium  (68) 

cochlea  (59) 

columella  (70) 

desidiosa  (73) 

expansa  (76) 

fragilis  (76) 

galbana  (74) 

gracilis  60 

humilis  (73) 

megasoma  60,  (67) 

serrata  (69) 
Limneus  (60) 

desidiosus  (73) 

emarginatus  (68) 

minutus  (72) 

ontariensis  (68) 

palustris  (76) 

stagnalis  (60) 

umbrosus  (77) 
Limnophysa  (60),  62 

holbolH  (74) 

palustris  60 

senegalensis  75 

vahlii  (74) 
Limnus  (61) 
Liria  (ill) 
Liriola  /// 

thersites  III 
Lucena  (22),  55 

oblonga  55 

pulchella  55 
Lucina  lenticula  140 
Lymnaea  jp,  60,  61,  62,  63,  66,  68,  72, 
100,  102 

acuta  80 

adelinae  78 

ampla  71,  72 

anticostiana  79 

appressa  (65) 

arenaria  63 

atkaensis  66 

auricularia  60, 61,  62,  64 

binneyi  6g,  70 


Lymnsea  bulimoides  78,  79 
canadensis  68 
caperata  79 

catascopium  77,  78,  79 
columella  70 
desidiosa  75,  75,  80 
emarginata  68, 69 
expansa  77 
ferruginea  73 
fossaria  80 
galbana  7J 
glaber  60,  62 
glabra  60 
gracilis  64 
hajdeni  77 
holboUi  74 
humilis  jj 
involuta  64 
jugularis  (65) 
kingi  64 
kirtlandiana  72 
lagorii  61,  63 
lanceata  72 
lepida  67 
malleata  75 
megasoma  63,  6j,  70 
mighelsi  68,  72 
nitida  75 
nuttalliana  77 
obrussa  73 
opacina  80 

palustris  62,  64,  68,  75,  j6,  78 
pereger  60 
perpollU  78 
petersi  66 
petitii  80 
pingelii  (75) 
preblei  70 
proxima  74,  77 
randolphi  66,  7/ 
reflexa  60,  62,  72,  ^j 
rowelli  76 
solida  78 
solidula  75 

stagnalis  61,  63,  6^,  66 
sumassi  66,  69,  71,  72,  (77),  78 
techella  78,  79 
tenuicostata  64 
traskii  74 


164 


INDEX 


Lymnaea  truncatula6o,  61, 62, 64, 7^,  73 

tryoni  74 

trjoniana  74 

vahlii  74,  75 

wormskioldi  (75) 

zrmanjse  61,  65 
Lymnaeidae  jp 
Ljmnaeus  (60) 

columellus  (70) 

emarginatus  (68) 
Lymnea  (60) 

cornea  (77) 
Lymneus  (60) 

caperatus  (79) 

desidiosus  (73) 

emarginatus  (68) 

galbanus  (73) 

humilis  (73) 

megasomus  (67) 

minutus  (72) 

reflexus  (77) 
Ljmnophysa  (61) 
Ljmnula  (60) 
Lymnus  (60) 
Lyogyrus  118 

granum  //^,  1 19 

lehnerti  (117) 

MacrocycHs  33 

vancouverensis  (34) 
Macrophysa  (100),  lot 
Margarita  oregonensis  (128) 
Margaritana  131 

falcata  132 

margaritifera  11, 132 
Melania  117 

canaliculata  (116) 

conica  (116) 

plicifera  (116) 

silicula  (116) 
Melantho  decisa  ( 125) 
Menetus  (81),  ^^,  86 

exacuous  91 

opercularis  92 
Microphysa  99 

lansingi  44 

pygmaea  (53) 

stearnsii  (44) 
Mouretia  (in) 


Muretia  (ill) 
Musculium  jayanum  139 

lenticula  140 

partumeium  139 

raymondi  138 

tenue  139 

transversum  139 

truncatum  140 
Mya  complanata  (133) 

margaritifera  (132) 

radiata  (126) 
Myxas  (104) 

Naiades  123 
Nauta  (104) 

hypnorum  (106),  (107) 

polaris  (107) 
Nautilina  (83) 
Nautilus  crista  (96) 

lacustris  97 
Neritostoma  jj,  (61) 

Odostomia  (115) 
Oligolimax  (36) 
Ompiialia  (61) 
Omphalolimnus  (6x),  63 
Omphiscola  60,  (61),  62 
Onchidella  jjz 

borealis  112,  113,  1I4 

carpenteri  113 

celtica  112,  113,  114 

floridana  114 
Onchidiidae  J12 
Onchidium  112,  114,  115 

boreale  (112) 

celticum  113 

nigricans  112 

Schramm!  114 

typhae  112 
Orbis  (81) 
Oreohelix  57 

cooperi  52 

itantoni  52 

strigosa  j/,  52 
Oxyloma  55 

hungarica  55 

P^ana  (36) 

Paludina  cincinnatiensis  118 


INDEX 


165 


Paludina  decisa  (125) 

emarginata  (ii8) 

grana  (118) 

hyalina  (91) 

limosa  (117) 

lustrica  120 

nuclea  (119) 

obtusa  (118) 

porata  (117) 

seminalis  (119) 

virens  (119) 
Paraspira  82,  86 
ParmacelHna  (36) 

vitrinaeformis  36 
Patella  (107) 

lacustris  107,  I08 
Patula  49 

aster iscus  (51) 

cronkhitei  (50) 

occidentalis  4q 

pauper  50,  51 

solitaria  (49) 

striatella  50 
Patulastra  pugetensis  (43) 
Periophthalmus  115 
Petasia  (39)  • 

fabricii  (41) 

fulva  40 

trochiformts  (40) 
Phenacarion  foliolatus  (47) 

hemphilli  (47) 
Phenacolimax  (36) 
Phjmesoda  dubia  (141) 

idahoensis  (141) 

scutellata  141 

virginica  141 
Physa  II,  63,  (81),  84,  p9,  (lOO),  lOI, 
102,  (104),  105,  107 

albofilata  (102) 

ampullacea  /oj 

ancillaria  102 

bullata  (103) 

columnaris  99,  loi 

contorta  99 

costata  100,  loi 

crassa  (102) 

elongata  (106) 

elongatina  107 

fontinalis  11,  99,  (102),  IQ5 


Physa  fragilis  (loi) 

glabra  (106) 

globosa  99 

guildingii  99,  lOO 

gyrina  lOl 

heterostropha  loi,  103 

hildrethiana  102 

hordeacea  los,  'i^ori 

hypnorum  (106) 

lata  (loi) 

lordi/o^,  103 

microstoma  99 

obesa  (102) 

oleacea  (102) 

parkeri  (102),  103 

philippii  (loi) 

plicata  (loi) 

polaris  107 

primeana  (loi) 

propinqua  103 

turrita  (106) 

vinosa  102 
Physastra  (61),  62,  64 

vestita  61,  64 
Physella  (99),  100 
Physidae  gg,  loi 
Physodon  (99),  100 
Physopsis  loo,  lOI 
Phyza  (99),  (104) 
Pierosoma  81,  85 

binneyi  87 

corpulentus  87,  88 

trivolvis  88 
Pisidium  3,  141 

abditum  (142),  (143) 

abyssomus  (143) 

abyssorum  (143) 

aequilaterale  (141) 

arcticum  (144) 

boreale  (144) 

compressum  (142) 

glaciale  (144) 

henslowianum  (145) 

idahoense  (141) 

nivale  (144) 

occidentale  (143) 

randolphi  (145) 

rotundatum  (143) 

scutellatum  (141) 


i66 


INDEX 


Pisidium  sibiricum  (144) 

steenbuchii  (143) 

ultramontanum  (144) 

variabile  (142) 

ventricosum  (143) 

virginicum  (141) 
Planaria  (83) 
Planella  (120) 
Planogyra  51 

asteriscus  5/,  122 
Planorbarius  (81) 
Planorbe  brun  80 
Planorbella  81,  85 

campanulatus  90 
Planorbina  81,  83,  84 

glabrata  86 
Planorbis   63,  80,  81,  82,  S3,  84,  102, 
(104),  105 

alabatnensis  92 

albus  83,  86,  (93),  94 

ammon  88 

andecolus  81 

arcticus  g6 

armatus  97 

armiger  97,  (98),  99 

armigerus  97,  (98) 

bellus  (90) 

bicarinatus  81,  84,  8j 

bilHngsi  (95) 

binneyi  87,  88,  89 

boissyi  82 

borealis  (93),  94 

brongniartiana  91 

buchanensis  92 

calculus  81 

calliogljptus  (92),  93 

campanulatus  81,  85,  90 

carinatus  82 

centervillensis  (92),  93 

complanatus  82,  85,  90 

concavus  (95) 

contortus  83,  86 

corneus  80,  81^  83,  84 

cornu-arietis  84 

corpulentus  5/ 

costatus  (96) 

crista  g6 

cristatus  (96) 

declivis  98 


Planorbis  deflectus  9^ 
dilatatus  92 
disjectus  89 
draparnaldi  94 
draparnaudi  94 
elevatus  (95) 
engonatus  (87) 
exacuous  gi,  92,  93 
exacutus  (91) 
fontanus  82,  86 
glabratus  86 
guadeloupensis  81 
hirsutus  pj,  94 
hispidus  83 
hornii  89,  90 
imbricatus  (96) 
lacustris  97 
lens  91 

lentus  (86),  (88) 
libanicus  82,  83 
Umophilus  95 
lineatus  97 
loryi  81 

macrostomus  (88),  8g,  90 
major  87 
marginatus  82 
megas  gi 

multivolvis  82,  85 
nathorsti  96 
nautileus  (96) 
nitidus  97 
obliquus  94 
occidentalis  89 
olivaceus  84 
opercularis  82,  86,  g2 
oregonensis  89,  (92),  93 
parallelus  (52) 
parvus  83,  86,  pj",  96 
planulatus  ga,  93 
rotundatus  82,  86 
rndentis  90,  91 
subcrenatus  (88),  89,  90 
traskii  88 

trivolvis  81,  85,  87,  88,  89, 90 
tumens  88,  89 
turritus  (106) 
umbilicatellus  g6 
umbilicatus  82,  85,  (96) 
vermicularis  pj 


INDEX 


167 


Planorbis  virens  94. 

vortex  82,  85 

vulgaris  82 

wheatleyi  97,  98 

yzabalensis  82,  86 
Plan  or  bu  la  (97),  98 

armigera  98 

christyi  99 
Plesiophysa  lOl 
Pleurocera  tj6 

canaliculata  lib 
PleuroHmnaea  (60),  63,  64 

tenuicostata  60 
Poeyia  (108) 

gundlachioides  108 
PoHta  (39) 

fulva  (40) 
Polygyra  24 

albolabris  26 

Columbiana  24,  34 

devia  24 

germana  ^J,  26 

labiosa  (24) 

megasoma  26 

monodon  26 

ptychophora  2^ 

santacruzensis  24 

townsendiana  2^ 
Poljgyrus  (83) 
Polyrhytis  (61),  63,  64 
Pomatiopsis  iig 

lapidaria  119,  (120) 
Pompholjx  63 
Primella  raymondi  (139) 
Pristiloma  44 

arctica  4s 

idahoense  44 

lansingi  44 

pilsbryi  44 

stearnsi  (44),  45 

stearnsii  44 

taylori  44 
Prophysaon  4b 

andersoni  4b 

coeruleum  ^7 

dubium  (47) 

fasciatum  (47) 

flavum  (46) 

foliolatum  ^7 


Prophysaon  hemphilli  (46),  47 

humile  47 

marmoratum  (46) 

obscurum  (47) 

pacificum  (46) 

pallidum  (46) 

suffusum  (46) 
Proptera  alatus  (127) 
Protancylus  109 
Pseudohyalina  minuscula  (43) 

pugetensis  (43) 
Pterosygna  131 
Pulmobranchia  loi 
Punctum  5j 

asteriscus  53 

clappi  51,  Ji 

conspectum  10,  JJ 

minutissimum  (53) 

pugetensis  (43) 

pygmaeum  S3 

randolphi  §3 
Pupa  alticola  (54) 

arctica  (32) 

arm  if  era  (27) 

badia  (28) 

bigfranata  (28) 

blandi  (28) 

columella  (54) 

contracta  (27) 

corpulenta  (29) 

costulata  (21) 

decora  (29) 

edentula  (54) 

exigua  (116) 

gouldii  (30) 

gredleri  (54) 

holzingeri  (28) 

hoppii  (29) 

lundstromi  (28) 

milium  (32) 

modesta  (29) 

pentodon  (28) 

pygmsea  (33) 

signata  (28) 

simplex  (54) 

steenbuchi  (29) 

superioris  (33) 
Pupidae  27 
Pupilla  28 


i68 


INDEX 


Pupilla  badia  (28),  (29) 

blandi  28 

muscorum  28,  (29) 
Pyramidula  49 

alternata  4g 

aster  iscus  ji 

cronkhitei  ^o,  51 

limitaris  4g 

randolphi  (53) 

ruderata  50,  51 

solitaria  4Q 

striatella  jo 

Quadrula  133 
heros  133 
hippopaea  133 
lachrjmosa  133 
plicata  ijj 
rubiginosa  134. 
undulata  133 

Radix  (60),  62,  63, 64,  65,  67,  68,  71,  72 

binneyi  69 

columella  70 

mighelsi  68 

randolphi  71 
Rivicola  (99) 

Sandria  65 
Saraphia  (115) 

tridentata  115 
Segmentaria  (97) 
Segmentina  97,  98 

armigera  g8 

christyi  99 
Selenites  33 

vancouverensis  (34) 
Semilimax  (35),  (36) 
Siphonaria  iii 

sipho  III 

thersites  /// 
Siphonariidse  iii 
Sphaeriidse  134,  145 
Spliaerium  134 

aureum  135 

cooperianum  (139) 

corneum  135 

dentatum  136,  13J 

emarginatum  138 


Sphaerium  fabale  137 

fabalis  (136) 

flavum  138 

jajanum  i3g 

lenticula  140 

medium  140 

nobile  137 

occidentale  136,  137 

partumeium  /jp 

patella  138 

primeanum  141 

raymondi  138 

rhomboideum  136,  141 

simile  134 

solidulum  136 

spokani 138 

stagnicola  140 

stamineum  136 

striatinum  13J 

sulcatum  (134) 

tenue  J3g,  140 

transversum  i3g 

truncatum  140 

tumidum  138 

walkeri  135 
Sphyradium  j^ 

edentulum  j^ 
Spiralina  (81) 
Spirodiscus  corneus  (81) 
Spirorbis  (82) 
Stagnicola  (60),  62,  64,  68,  71,  72,  74 

adelinae  78 

•nticostiana  79 

bulimoides  79 

caperata  79 

catascopium  77 

communis  (76) 
emarginata  68 

palustris  76 

perpolita  78 

reflexa  77 
Stenotrema  germanum  (25) 
Strepomatidae  116 
Striatura  milium  (43) 
Strobila  labjrinthica  2f 
Strophitus  127 

edentulus  (127) 
rugosus  127 
Succinea  (55),  55,  71,  105 


INDEX 


169 


Sncdnea  aUskaiu  58 

annexa  (59) 

aurelia  (59) 

avara  55,  56, 57 

campestris  (58) 

chrjsis  10,  59 

decampi  (56) 

dunkeri  55 

elegans  55 

greeri  (58) 

gronlandica  ^J 

grosvenori  // 

hawkinsi  J7 

haydeni  (56) 

lineata  (59) 

minor  (56) 

nuttalliana  /5 

obliqua  s8 

oblonga  55 

oregonensis  j'd 

ovalis55,  (56),  (58),  59 

pfeifferi  55 

putris  55 

retusa  (56),  57,  58 

rusticana  j5 

silHmani  57 

totteniana  55 

vermeta  (57) 

verrilli  57 

wardiana  (57) 
Succineidae  55 
Succinia  (55) 
Sjmphjnota  131 

complanata  131 

costata  /J/ 

katherinae  131 

Tanousia  (61),  62,  65 

Tapada  (55) 

Taphius  (81),  85 

Teba  (39) 

Tellina  henslowana  (145) 

virginica  (141) 
Torquis  83,  86 

arcticus  96 

nathorsti  96 

parvus  95 

umbilicatellus  96 

vermicularis  95 


Trimusculus  (iii) 
Trochilus  terrestris  mortoni  40 
Trochlea  (83) 
Trochovitrina  (36) 
Trochula  40 
Trochulus  (40) 

trochiformis  (41) 
Trochus  (39) 

terrestris  (40) 
Trophidiscus  (82) 
Tropidina  (120),  1 21 
Tropidiscus  (81),  82,  85 
Tropidocyclas  henslowana  145 
Truella  (55) 

elongata  55 
Turbo  (104),  (115) 

muscorum  (28) 

nautileus  (96) 

stagnalis  (106) 

Unio  II,  133 
alatus  (126) 
asperrimus  (133) 
borealis  (126) 
complanatus  (132),  /jj 
costatus  (133) 
crassus  (126),  (133) 
dahuricus  (132) 
ellipsiformis  (126) 
elongatus  (132) 
falcatus  (132) 
flavus  (134) 
gracilis  (127) 
heros  (133) 
hippopaeus  (133) 
katherinje  (131) 
lachrymosus  (133) 
ligamentinus  (126) 
luteolus  (125) 
mongolicus  (132) 
multiplicatus  (133) 
pictorum  13 
pUcatus  (133) 
quadrulus  (133) 
radiatus  (126) 
rectus  (126) 
rubiginosus  (134) 
sinuatus  (132) 


I70 


INDEX 


Unio  spatulatus  (126) 
trigonus  (134) 
undulatus  (133) 
ventricosus  (125) 

Vallonia  22 

albula  2^ 

asiatica  23 

costata  23 

gracilicosta  23 

minuta  {22") 

pulchella  22,  23 

rosalia  (23) 
Valvata85,  (120) 

carinata  (121) 

confusa  (121) 

cristata  120,  122,  124 

helicoidea  123 

humeralis  121 

jelskii  120,  121 

lewisi  123 

mergella  124 

minuta  120 

nylanderi  122 

piscinalis  120,  121,  124 

sibirica  124 

simplex  (121),  122,  123 

sincera  122,  (123) 

striata  (123) 

tricarinata  120,  I2i,  I22 

unicarinata  (l2r) 

virens  124. 
Valvatidae  120 
Valvearius  (120) 
Velifera  36 
Velletia  (108),  109 
Velutinopsis  (61),  62,  65 
Vertigo  3,  2g 

approximans  (31) 

arctica  32 

arthuri  (31) 

binnej'ana  J/ 

bollesiana  (30) 

borealis  30 

callosa  (33) 

castanea  (29) 

Columbiana  JO 

elatior  (31) 

gouldii  30 


Vertigo  hoppii  2g 

krauseana  32 

lagganensis  (31) 

milium  32,  33 

modesta  2g 

ovata  31,  J2 

parietalis  (29) 

pentodon  (28) 

pygmaeajj 

simplex  (54) 

ventricosa  31 
Vertilla  milium  (32),  33 
Vesica  (59) 
Vitrea  38,  (40) 

binneyana  3g 

fulva  (41) 

indentata  jp 

nitidula  jp 

radiatula  j5 
Vitrinajj,  (36),  37 

Alaskana  37,  38 

americana  (37) 

angelicae  j<5,  37 

berjilina  37 

bicolor  36 

conoidea  36 

diaphana  36 

exilisj/,  (38) 

lederi  36 

limpida  J7 

major  36 

pauluccise  36 

pellucida  36,  (37) 

pfeifferi  (37) 
Vitrinozonites  36 
Vitrinus  {35) 
Vivipara  11 
Viviparidae  J24 
Vortex  81 
Vorticifex  63 

Zagrabica  (61),  65 

brusiniana  65 

naticoides  61 
Zonites  (39) 

conspectus  (53) 

fulvus  (40) 

lansingi  44 

nitidulus  (39) 


INDEX  171 

Zonites  stearnsii  (44)  Zonitoides  pugetensis  43 

viridulus  (38),  39  randolphi  43 

Zonitidae  35  Zoogenites  21 
Zonitoides  42  harpa  12,  21,  22,  122 

arboreus  42  Zua  lubrica  {33) 

milium  (43)  lubricoidea  (33) 

minusculus  43  Zurama  (22) 

nitidus  4a 


HYDROIDS  OF  THE  EXPEDITION 


The  following  paper  on  the  Hydroids  of  the  Expedition,  by  Pro- 
fessor C.  C.  Nutting,  of  the  University  of  Iowa,  was  originally  pub- 
lished in  the  Proceedings  of  the  Washington  Academy  of  Sciences, 
vol.  Ill,  pp.  157-216,  May  11,  190 1,  It  is  here  reprinted  from  the 
same  electrotype  plates,  so  that  it  may  be  quoted  exactly  as  if  it  werfe.  the 
original.  The  original  pagination  has  been  preserved  and  transferred 
to  the  inner  or  hinge  side  of  the  page,  where  it  is  enclosed  in  brackets, 
thus  [159];  while  the  consecutive  pagination  of  the  present  volume 
has  been  added  in  the  usual  place.  In  the  plates  the  original  number 
and  running  headline,  slightly  abbreviated,  have  been  preserved  [in 
brackets],  while  the  volume  designation  and  serial  plate  number  have 
been  added  in  the  usual  place.  The  original  text  references  to  the 
plates  are  unchanged.  The  present  headpiece  and  title  have  been  sub- 
stituted for  the  running  heading  of  the  Academy's  Proceedings  and 
the  original  title,  which  was :  Papers  from  the  Harriman  Alaska 
Expedition.  XXL  The  Hydroids.  No  other  alterations  have 
been  made.  Editor. 


(174) 


HYDROIDS  OF  THE  EXPEDITION 


BY  C.  C.  RUTTIBQ 

CONTENTS 

Introduction 175 

Geographic  distribution 176 

Systematic  discussion 181 

INTRODUCTION. 

The  collection  of  Hydroida  secured  by  the  Harriman  Ex- 
pedition is  of  exceptional  interest,  and  proves  to  be  one  of  the 
most  important  and  most  extensive  collections  of  these  beautiful 
forms  of  marine  life  thus  far  made  in  Alaskan  waters.  Our  pre- 
vious knowledge  of  the  Hydroid  fauna  of  this  region  rested  almost 
exclusively  on  the  collection  made  by  Dr.  W.  H.  Dall  and  his 
associates  during  the  years  1871-1874  and  reported  on  by  Dr.  S. 
F.  Clark. ^  The  number  of  species  listed  in  Clark's  report  is  41, 
in  which  was  included  Coppinia  arcta^  now  known  to  be  merely 
the  gonosome  of  Lafoea.  Of  these  40  species,  15  are  well  known 
British  forms,  and  only  one  was  then  known  from  the  Atlantic 
coast  of  the  United  States.     The  remaining  24  species  were  new. 

^  Report  on  the  Hydroids  collected  on  the  coast  of  Alaska  and  the  Aleutian 
Islands  by  W.  H.  Dall,  U.  S.  Coast  Survey,  and  party,  from  1871  to  1874, 
inclusive.     Proc.  Acad.  Nat.  Sciences,  Philadelphia,  1876. 

[157]  (»75) 


176  NUTTING  [158] 

In  1878  C.  Mereschkowsky  ^  added  a  single  species  to  the 
Alaskan  fauna,  bringing  the  total  up  to  41. 

No  other  additions  were  made  until  1899,  when  I  added  eight, 
of  which  three  were  well  known  British  species  and  five  were 
new.^  That  made  a  total  of  49  species  reported  prior  to  the 
Harriman  Expedition. 

The  collection  here  treated  of  comprises  53  species,  24  of 
which  had  been  previously  reported.  Of  the  remainder,  9  were 
previously  recorded  from  other  localities,  and  20  are  new. 
Thus  the  Harriman  Expedition  has  added  about  60  percent  to 
the  number  of  species  hitherto  known  from  Alaskan  waters. 
More  than  half  of  the  species  secured  are  new  to  Alaska  and 
nearly  40  percent  are  new  to  science. 

The  whole  number  of  species  of  hydroids  now  known  from 
Alaska  is  78.  Considering  the  small  amount  of  collecting  that 
has  been  done  in  that  region,  compared  with  the  extensive  ex- 
plorations of  the  coasts  of  Europe  and  the  Atlantic  coast  of  the 
United  States,  one  may  confidently  expect  that  the  waters  of 
the  far  Northwest  will  prove  to  be  very  rich  in  hydroid  life.  . 

GEOGRAPHIC    DISTRIBUTION. 

A  table  is  here  given  to  indicate,  first,  the  localities  at  which 
each  species  was  collected  by  the  Harriman  Expedition,  and 
second,  the  extent  to  which  Hydroids  have  been  distributed  south- 
ward along  meridional  lines  from  what  appears  to  have  been 
a  polar  center  of  distribution.  No  attempt  has  been  made  to 
represent  the  complete  distribution  of  the  species. 

A  glance  at  the  part  of  the  table  showing  the  distribution  as 
represented  in  the  collection  secured  by  the  expedition,  shows 
an  apparent  poverty  of  the  Hydroid  fauna  of  the  western,  as 
compared  with  the  eastern,  portion  of  the  territory  explored. 
For  convenience  in  such  comparison  the  stations  are  arranged 
consecutively  from  east  to  west.  The  largest  series  were  ob- 
tained at  Berg  Inlet  in  Glacier  Bay ;  Yakutat  Bay  ;  and  at  Orca 
in  Prince  William  Sound.  These  localities  are  all  in  deep  bays, 
sheltered   from  storms  and  surrounded  by  rocky  shores.     On 

*  New  Hydroida  from  Ochotsk,  Kamtschatka,  and  other  parts  of  the  North 
Pacific  Ocean.    Annals  and  Mag.  Nat.  Hist.,  Dec,  1878. 

«Hydroida  from  Alaska  and  Puget  Sound.  Proc.  U.  S.  Nat.  Museum,  Vol. 
XXI.     (No.  1171.) 


GEOGRAPHIC    DISTRIBUTION    OF   THE    HYDROIDS    COLLECTED    BY 
THE    HARRIMAN    EXPEDITION. 


Name.» 

Distribution  of  Specimens  in  the  Ham- 
man  Collection. 

General  Distribution. 

i 

3 
1— 1 

i 

"5 

1 

s 

3 

>< 

a 
O 

•i 
1 

•6 

1 

1 

a 

1 

X 
•g 

3 

0 

V 

a 
o 

a 

B 
O 

•& 

< 

o 
1 

d< 

o  o 

|i 

a.  en 

1 

1 

< 

Syncoryne  eximia. 
*Coryne  brachiata. 
*Garveia  annulata. 

+ 

+ 

-h 

+ 
+ 

+ 

+ 

Garveia  nutans. 

+ 

+ 

Eudendrium  vaginatum. 
*Tubularia  harrimani. 

+ 

+ 

+ 

+ 

+ 

+ 

♦Campanularia  ritteri. 

Campanularia  denticulata. 

Campanularia  verticillata. 

Campanularia  lineata. 

Campanularia  speciosa. 

Campanularia  urceolata. 
^Campanularia  reduplicata. 
♦Campanularia  regia. 

Clytia  caliculata. 

Clytia  compressa. 

Obelia  plicata. 

Obelia  dichotoma. 

+ 

+ 

+ 

+ 

+ 

+ 

+ 
+ 

+ 

+ 

+ 

+ 
+ 

+ 
+ 

4- 

-f 

+ 

+ 

+ 

+ 

+ 

+ 

4- 

+ 

+ 

+ 

+ 

+* 

+ 

+ 

*Obelia  borealis. 

+ 

*Obelia  dubia. 

..... 

+ 

" 

Hebella  pocillum. 
*Gonothynea  inornata. 
♦Campanulina  rugosa. 

Calycella  syringa. 

Lafoea  dumosa. 

+ 

+ 

+ 

+ 

+ 

+ 

+ 

+ 

+ 

+ 

+ 

+ 
+ 
+ 
+ 

+ 
+ 

+ 

4- 

+ 
+ 

+ 
+ 
+ 
+ 

, 

+ 

Lafoea  gracillima. 
Lafoea  fruticosa. 

+ 

+ 

+ 
-f 
+ 

*Lafoea  adherens. 

+ 

*Grammaria  immersa. 

+ 

Filellum  serpens. 
Halecium  halecinum. 

+ 

+ 
+ 
+ 
+ 

+ 

+ 
+ 
+ 

+ 

+ 

Halecium  muricatum. 

+ 

Halecium  scutum. 

+ 

+ 

*Halecium  reversum. 

-h 

+ 

*Halecium  robustum. 

+ 

+ 
+ 

*Halecium  ornatum. 

♦Halecium  speciosum. 

Sertularella  tricuspidata. 

Sertularella  polyzonias. 
*Sertularella  saccata. 

4- 
+ 

+ 

+ 

+ 

+ 
+ 

+ 
+ 

t 

+ 
+ 

+ 

+ 

+ 

+ 



Thuiaria  argentea. 
Thuiaria  similis. 

+ 

+ 

+ 
+ 

+ 

Thuiaria  variabilis. 

+ 



Thuiaria  cupressoides. 
♦Thuiaria  coei. 

+ 

+ 
+ 

Thuiaria  fabricii. 

+ 

+" 

+ 



+ 



+ 

Thuiaria  turgida. 

+ 

+ 

Thuiaria  gigantea. 
Thuiaria  thuiarioides. 



"+'" 

+ 

♦Thuiaria  elegans. 
♦Thuiaria  costata. 

+ 

+ 

+ 

Plumularia  lagenifera. 

+ 

+ 

+ 
+ 

20 

Plumularia  palmeri. 
Totals. 

lO 

4 

12 

IS 

13    8 

3 

I 

4 

19 

I'g    14 

25 

'  Species  marked  by  a  ♦  are  new. 


178  NUTTING  [l^l 

account  of  the  presence  of  perpetual  ice  in  the  form  of  glacier 
fronts  and  bergs,  the  water  must  be  very  cold  the  year  around. 
Such  a  combination  of  conditions  is  particularly  favorable  to 
Hydroid  life  and  accounts  for  the  remarkably  rich  collections 
made  at  these  places  and  also  for  the  presence  of  so  many  arc- 
tic species.  In  this  connection  it  is  interesting  to  note  the  fol- 
lowing paragraph  written  about  twenty  five  years  ago  by  Dr. 
Dall :  "The  material  derived  from  the  northwestern  coasts  of 
America,  from  Cook's  Inlet  south  and  east,  indicates  a  series  of 
Arctic  colonies  in  favored  localities,  the  future  exploration  of 
which  offers  a  labor  of  the  highest  interest.  These  colonies  are 
situated  where  the  depth  of  water,  the  drippings  of  glaciers,  and 
the  high  and  adjacent  shores  of  the  Great  Archipelago  combine 
to  reduce  the  temperature  of  the  water  below  its  apparently 
normal  isotherm.  Cook's  Inlet  affords  one  of  them,  one  exists 
in  the  Gulf  of  Georgia,  and  others  only  await  further  explora- 
tion."^ It  should  be  noted,  however,  that  nearly  all  of  the 
Arctic  species  are  well  known  forms  belonging  to  the  '  Holarctic 
Province '  of  authors,  and  that  these  species  are  of  practically 
continuous  distribution  on  all  coasts  in  northern  regions  so  far 
as  explored. 

In  the  same  paper,  Dr.  Dall  divides  the  coasts  of  America 
from  Monterey,  California,  north  and  west,  into  three  faunal 
areas,  as  follows  :  (a)  the  Oreg'onian,  extending  from  Monterey 
to  the  Shumagin  Islands ;  (3)  the  Aleutian^  extending  from  the 
Shumagin  Islands  to  the  end  of  the  Aleutian  chain,  and  north- 
ward to  the  winter  line  of  floating  ice  in  Bering  Sea ;  {c)  the 
Arctic^  limited  on  the  shore  line  to  the  winter  line  of  floating 
ice  and  passing  southward  indefinitely  in  deep  water. 

This  paper  deals  chiefly  with  what  Dr.  Dall  would  call  the 
Oregonian  Fauna,  only  seven  species  having  been  secured  to 
the  westward  of  the  Shumagin  Islands.  Of  these  seven  species 
five  are  also  found  in  his  Oregonian  Fauna,  and  the  other  two 
are  new  and  known,  thus  far,  from  only  one  locality. 

Dr.  Clark,  in  reporting  on  the  collection  made  by  Dr.  Dall, 
enumerates  25  species  that  occur  west  and  north  of  the  Shu- 
magin Islands.     Of  these  25  species  we  now  know  that  sixteen 

'Proc.  Acad.  Nat.  Sciences,  Philadelphia,  p.  206,  1876. 


[l6l]  THE    HYDROIDS  l79 

also  occur  to  the  eastward  of  the  Islands,  while  five  have  not 
been  reported  from  any  locality  other  than  the  ones  where  they 
were  originally  discovered.  Our  present  knowledge  therefore 
does  not  support  the  validity  of  Dr.  Dall's  division  of  faunae  at 
the  Shumagin  Islands.  It  rather  indicates  a  continuity  of  fauna 
from  southern  Alaska  to  the  end  of  the  Aleutian  chain.  Hydroid 
life  appears  to  decrease  as  we  go  westward,  but  this  may  be  only 
apparent  and  due  to  the  more  extensive  exploration  of  the  shores 
east  of  the  Aleutian  Islands. 

Dr.  Dall  extends  his  Oregonian  fauna  down  to  Monterey, 
California.  Reasoning  again  merely  from  the  known  distribu- 
tion of  hydroids,  it  would  seem  that  Puget  Sound  is  a  natural 
region  of  demarcation  between  faunae,  although  the  region  from 
Puget  Sound  to  San  Francisco  has  been  very  little  explored. 
In  1876  Dr.  Clark  published  a  paper  on  '  The  Hydroids  of  the 
Pacific  Coast  of  the  United  States  south  of  Vancouver  Island,'  * 
in  which  he  gives  a  list  of  twenty-four  species ;  of  these  only 
two,  Lafosa  duniosa  and  Sertularia  argentea,  have  as  yet  been 
reported  north  of  Puget  Sound.  The  same  author,  in  reporting 
on  Dr.  Dall's  collections  from  Alaska,  notes  as  one  of  the  main 
points  of  interest,  the  "  small  number  of  species  that  are  com- 
mon to  the  Alaskan  coast  and  the  western  shores  of  the  United 
States  from  Vancouver  Island  southward.^  In  1899  the  present 
writer  published  a  paper  on  '  Hydroida  from  Alaska  and  Puget 
Sound ' '  in  which  it  appears  that  out  of  twenty-two  species  from 
Puget  Sound,  only  four  have  been  reported  farther  south,  while 
fifteen  are  now  known  to  occur  in  Alaska.  In  the  same  year 
Mr.  G.  N.  Calkins  published  a  paper  entitled  '  Some  Hydroids 
from  Puget  Sound,' ^  in  which  some  thirty  species  are  noted, 
only  two  of  which  are  known  to  occur  south  of  Puget  Sound. 

From  this  study  of  the  distribution  of  the  Hydroids  of  the 
northwest  coast  of  America,  therefore,  I  am  strongly  persuaded 
that  the  region  south  of  Puget  Sound  constitutes  one  distinct 
faunal  area,  and  that  the  region  from  Puget  Sound  north  and 
west  to  the  end  of  the  Aleutian  chain  constitutes  another  un- 

1  Trans.  Conn.  Acad.  Sci.,  Vol.  iii,  pp.  250-251,  1876. 
*Proc.  Acad.  Nat.  Sciences,  Philadelphia,  p.  212,  1876. 
8Proc.  U.  S.  Nat.  Museum,  Vol.  xxi,  No.  1171,  1899. 
*Proc.  Bost.  Soc.  Nat.  Hist.,  Vol.  xxviii,  No.  13,  1899. 


l8o  NUTTING  [162] 

broken  faunal  area  that  might  properly  be  designated  as  Alaskan. 
From  the  number  of  arctic  species  included  in  this  area  it  is  not 
improbable  that  it  extends  northward  along  the  shores  of  Bering 
Sea. 

Dr.  Clark  agrees  with  Dr.  Dall  that  there  is  a  distinct  faunal 
difference  between  the  region  east  of  the  Shumagin  Islands  and 
that  west  of  them.  The  material  added  since  the  publication  of 
his  paper,  however,  seems  to  prove  that  this  difference  is  only 
apparent  and  due  solely  to  lack  of  exploration. 

The  most  important  thing  to  be  noted  in  that  part  of  the  table 
devoted  to  general  distribution  is  the  Holarctic  distribution  of  a 
number  of  species.  Of  the  eighteen  species  known  to  occur  in 
the  Arctic  region,  no  less  than  fifteen  also  occur  on  the  European 
coast,  fourteen  on  the  Atlantic  coast  of  the  United  States,  and 
thirteen  on  the  Pacific  coast  as  far  south  as  Puget  Sound.  An 
examination  of  the  table  shows  further,  that  the  Hydroid  fauna 
of  Alaska,  as  represented  by  the  Harriman  collection,  includes 
fifty-three  species  in  all,  of  which  eighteen  are  Arctic  in  fact, 
having  been  secured  in  Arctic  waters ;  four  others  are  in  all 
probability  Arctic,  being  found  both  in  European  and  American 
waters ;  four  are,  so  far  as  is  known,  confined  to  the  Alaskan 
and  Pacific  coast  south  to  Puget  Sound ;  twenty-five  are  thus  far 
known  from  Alaska  only,  and  two  are  Californian.  If  we  rec- 
ognize the  Alaskan  faunal  region  as  extending  to  Puget  Sound, 
and  include  those  species  actually  known  to  be  Arctic,  together 
with  those  in  all  probability  Arctic,  in  a  group  which  may  justly  be 
called  Arctic,  the  following  significant  analysis  of  the  faunal  rela- 
tions of  the  collection  may  be  made :  Alaskan  species,  twenty- 
nine  ;  Arctic  species,  twenty-two  ;  Californian  species,  two.  This 
shows  that  fifty-five  percent  of  the  hydroid  fauna  as  a  whole  is 
peculiar  to  Alaska,  but  that  there  has  been  a  strong  invasion  from 
the  Arctic  regions  of  the  Holarctic  species  constituting  about 
forty-one  percent  of  the  collection,  and  that  only  two  species, 
or  less  than  four  percent,  are  Californian.  If  all  the  species 
known  to  occur  in  Alaska  were  included  in  the  computation  the 
result  would  be  a  larger  percentage  of  Alaskan  species,  a  cor- 
responding decrease  of  the  Arctic  species,  and  the  addition  of 
one  or  two  Californian  species. 


[163]  THE    HYDROIDS  181 

SYSTEMATIC    DISCUSSION. 

The  writer  deems  it  unnecessary  to  attempt  a  complete  syn- 
onymy of  the  well  known  European  species  contained  in  the 
Harriman  collection  and  considers  it  sufficient  to  give,_;fr5/,  and 
in  all  cases,  the  original  reference  to  the  species ;  second^  all 
obtainable  references  to  the  occurrence  of  the  species  on  the 
Pacific  Coast  of  America,  and,  thirds  a  reference  to  verify  the 
*  General  Distribution '  as  given  in  the  table  just  discussed.  In 
this  latter  case  only  one  reference  will  be  given  to  verify  the 
occurrence  of  a  given  species  in  each  of  the  regions  included 
in  the  right  hand  portion  of  the  table. 

As  to  the  classification  employed  in  this  report,  it  seems  best, 
on  the  whole,  to  pursue  a  conservative  course,  following  pretty 
closely  the  lines  laid  down  by  the  able  British  naturalists, 
Hincks  and  Allman.  While  it  is  true  that  the  classification  is 
in  an  unsatisfactory  state,  the  writer  does  not  feel  that  a  thor- 
ough revision  of  the  entire  group  of  Hydroida  should  be  at- 
tempted here,  and  frankly  confesses  his  conviction  that  recent 
attempts  in  that  direction  have  not  been  successful,  though  each 
contains  valuable  suggestions.  Levinsen,  for  example,  has 
made  a  notable  contribution  to  our  knowledge  of  the  Campanu- 
linidae  in  his  able  and  careful  exposition  of  the  differences  in 
the  opercula  of  various  species,  but  his  genera  founded  solely  on 
these  structures  appear  to  be  artificial,  as  usually  happens  when 
a  single  character  is  made  the  basis  of  classification.^  In  his 
terse  characterization  of  the  genera  of  Sertularidae  this  author 
has  been  most  fortunate,  as  well  as  in  his  masterly  clearing  up 
of  the  mystery  concerning  the  gonosome  of  Lafoea. 

Schneider,^  also,  has  attempted  to  rearrange  the  Hydroida  on 
a  logical  basis.  Instead  of  multiplying  groups,  as  has  been  the 
tendency  of  late,  he  has,  in  my  opinion,  gone  far  to  the  other 
extreme,  uniting  families  that  almost  any  other  student  acquainted 
with  the  group  would  regard  as  surely  distinct.  It  seems  un- 
likely that  he  will  be  followed  in  uniting  such  groups  as  the 
Tubularidae  and  Pennaridae  in  a  single   family,  although  one 

'Meduser,  Ctenopherer  og  Hjdroider  fra  Gronlands  Vestkyst,  Copenhagen, 
1893. 

*  Hydropolypen  von  Rovigno,  nebst  iibersicht  iiber  das  system  der  hydro- 
polypen  in  allgemeinen.     Zool.  Jahrb.,  Syst.  Abth.,  Vol.  x,  1897. 


l82  NUTTING  [164] 

writer,  Calkins/  has  followed  his  classification  quite  closely,  and 
includes  representatives  of  what  would  ordinarily  be  regarded  as 
at  least  eleven  families  in  five  families  as  defined  by  Schneider. 
It  is  not  likely  that  classifications  will  ever  represent  anything 
but  individual  opinion,  and  it  is  probable  that  there  will  always 
be  two  sets  of  extremists  who  on  the  one  hand  will  be  too  ready 
to  multiply  groups,  and  on  the  other  will  be  too  conservative  to 
recognize  real  progress.  The  Hydroida  offer  unusual  difficul- 
ties and  consequently  students  of  that  group  find  agreement, 
even  along  the  most  general  lines,  practically  impossible.  The 
objective  point  of  systematic  discussion  has  been  the  attainment 
of  a  system  of  classification  by  which  genera  could  be  distin- 
guished by  means  of  the  trophosome  alone.  This  end,  although 
in  theory  greatly  to  be  desired,  appears  to  be  unattainable.  The 
writer  has  chased  this  will-o-the-wisp  for  years,  and  is  ready  to 
abandon  its  pursuit  as  unprofitable.  Abler  men  have  had  the 
same  experience,  and  it  appears  to  be  pretty  well  established 
that  in  practice  we  must  base  generic  distinctions  on  the  gono- 
some alone,  although  the  judgment  of  students  will  inevitably 
differ  as  to  the  extent  to  which  this  can  be  profitably  done. 
Botanists  have  encountered  the  same  difficulty  in  their  study  of 
the  lower  plants,  such  as  the  fungi,  and  have  come  to  the  same 
conclusion.  In  neither  case  has  nature  been  working  for  the 
convenience  of  naturalists,  and  the  fact  should  be  accepted 
without  a  bootless  chase  after  the  unattainable. 

G  TMNOBLASTEA. 
Hydroida  in  which  well  differentiated  hydrothecae  and  gonangia  are 
not  present.     What  might  be  called  '  pseudo-hydrothecae  '  are  found  in 
some  species  as  in  Eudendrium  vaginatum   (see  description  of  that 
species  on  pages  167-168). 

Family  CORTNID^E. 

Trophosome. — Hydranth  with  a  terete  body  and  proboscis  and  scat- 
tered capitate  tentacles  only. 

Gonosome. — Fixed  sporosacs,  or  free  medusze  with  a  very  long  manu- 
brium, four  marginal  tentacles  and  four  sense-bulbs  with  eye-spots. 

^Some  Hydroids  from  Puget  Sound,  Proc.  Bost.  Soc.  Nat.  Hist.,  Vol. 
XXVIII,  No.  13,  1899. 


[165]  THE    HYDROIDS  183 

CORYNE. 

Trophosome. — Characters  of  the  family. 

Gonosome. — Reproductive  elements  produced  in  fixed  sporosacs 
growing  on  the  hydranth  body. 

CORYNE  BRACHIATA  sp.  nov. 
(Plate  XIV,  figs.  1,2.) 

Trophosome. — Colony  forming  a  dense  tuft  of  irregularly  branching 
stems,  sometimes  attaining  a  height  of  about  ^  inch.  Stems  and 
branches  profusely  and  regularly  annulated  throughout,  fairly  stout  ex- 
cept at  the  proximal  ends  w^here  they  taper  gradually  to  their  point  of 
origin ;  distal  ends  of  many  of  the  branches  bear  a  more  or  less  regular 
whorl,  or  radiating  cluster,  of  annulated  branchlets  just  below  the 
hydranth  body,  reminding  one  of  the  whorls  of  cirri  around  the  stems 
of  the  stalked  crinoids.  Hydranths  large,  with  long,  slender  body  and 
proboscis  and  numerous  (20-35)  capitate  tentacles  arranged  in  a 
scattered  or  sub-verticillate  manner  over  nearly  the  whole  surface. 

Gonosome. — Gonophores  very  numerous,  borne  among  the  tentacles 
on  the  hydranth  bodies,  globular  in  outline  and  showing  no  traces 
of  radial  canals  or  other  medusoid  structures.  The  specimens 
secured  were  females  and  the  gonophores  were  packed  full  of  develop- 
ing ova. 

Distribution. — All  the  specimens  were  secured  in  Yakutat  Bay, 
Alaska,  by  Dr.  W.  R.  Coe  of  the  Harriman  Expedition. 

This  interesting  species  seems  to  be  nearest  to  C.  pusilla  Gaertner,  if 
Allman  has  properly  identified  that  species.  It  differs  from  other 
members  of  the  genus  in  the  curious  whorl  of  short  branchlets  which 
bear  neither  hydranths  nor  gonophores  and  are  situated  a  short  distance 
below  the  terminal  hydranth  of  the  stem  or  branch  to  which  they  are 
attached.  Another  character  not  shown  in  the  figures  of  this  genus 
published  by  Hincks  and  Allman,  is  the  narrowing  at  the  proximal 
ends  of  the  stems  and  branches.  The  specimens  were  found  immersed 
in  sponge  so  far  that  only  the  hydranths  extended  above  the  surface  of 
the  sponge. 

SYNCORYNE. 

Trophosome. — Characters  the  same  as  those  given  for  the  family. 

Gonosome. — Reproductive  elements  produced  in  free  medusas  with 
a  long  manubrium  and  four  marginal  tentacles,  each  having  a  sense 
bulb  with  an  eye-spot  at  its  base. 


184  NUTTING  [166] 

SYNCORYNE  EXIMIA  Allman. 
(Plate  XIV,  figs.  3,  4.) 

Coryne  eximia  Allman,  Annals  and  Mag.  Nat.  Hist.,  3d  Series,  Vol.  iv,  p. 

141.     Aug.,  1859. 
Syncoryne  eximia  Allman,  Annals  and  Mag.  Nat.  Hist.,  3d  Series,  Vol.  xiil, 

p.  357.     May,  1864. 

This  appears  to  be  the  first  record  of  the  occurrence  of  this  species 
in  American  waters.  There  are  many  specimens  in  the  collection,  but 
all  are  from  the  same  locality. 

Distribution. — Juneau,  Alaska  (Harriman  Expedition)  ;  Great 
Britain  (Allman  and  Hincks)  ;  Lofoten  Islands,  Norway  (Sars). 

Family  BIMERID^^. 
Trophosome. — Hydranths  with  a  conical  or  dome-shaped  proboscis, 
around  the  base  of  which  is  a  whorl  of  filiform  tentacles. 
Gonosome. — Sexual  products  developed  in  fixed  sporosacs. 

GARVEIA. 

Trophosome. — Colony  branched  ;  perisarc  conspicuous. 

Gonosome. — Gonophores  borne  on  distinct  branchlets  which  have  a 
chitinous  investment  ending  in  a  cup-like  expansion  just  below  the 
gonophore. 

GARVEIA  NUTANS  Wright. 

Garveia  nutans  Wright,   Edinburgh  New  Phil.  Jour.,  p.  109.     July,  1859. 
Eudendriutn  bacciferum  Allman,  -Annals  and  Mag.  Nat.   Hist.,  3d  Series, 
Vol.  IV,  p.  52,  July,  1859. 

This  is  another  species  that  has  not  before  been  reported  from 
American  waters.  The  specimens  were  fragmentary,  making  the 
identification  somewhat  uncertain,  although  I  have  little  doubt  of  its 
correctness. 

Distribution. — Berg  Inlet,  Glacier  Bay,  Alaska.  (Harriman  Ex- 
pedition.)    Originally  described  from  the  British  Coast. 

GARVEIA  ANNULATA  sp.  nov. 
(Plate  XV,  figs.  I,  2.) 
Trophosome. — Colony  attaining  a  height  oi  1}^  inches,  consisting  of 
a  number  of  closely  aggregated  and  sparingly  and  irregularly  branched 
stems.  Stems  strongly  and  evenly  annulated  throughout,  the  perisarc 
expanding  distally  into  thin  chitinous  pseudo-hydrothecse  which  cover 
the  hydranth  body  nearly  to  the  level  of  the  tentacles.    Hydranths  with 


[i67] 


THE    HYDROIDS 


a  conical,  or  rather  conoid,  proboscis  and  about  sixteen  tentacles  all  of 
which  appear  to  be  held  more  or  less  erect. 

Gonosome. — Gonophores  borne  either  on  the  stem  or  hydrorhiza, 
more  frequently  the  latter,  oval  in  shape,  borne  on  pedicels  enveloped 
in  a  chitinous  perisarc  which  ends  in  a  slightly  expanded  collar  a  little 
below  the  gonophore.  The  specimens  collected  were  female  and  the 
gonophores  were  packed  with  apparently  mature  ova. 

Color. — The  label  accompanying  the  specimens  bore  the  following 
statement:   "Bright  orange  throughout,  heads,  stems  and  all." 

Distribution. — ^Yakutat  and  Sitka,  Alaska.  Collected  by  the  Har- 
riman  Expedition  in  considerable  quantities. 

This  species  can  be  sharply  distinguished  from  its  British  relative 
by  the  very  distinct  and  beautiful  annulation  which  covers  the  entire 
stem  and  branches.  It  is  much  less  extensively  branched  than  the  British 
species,  and  the  gonophores  are  more  generally  borne  on  the  roots. 

The  structure  that  I  have  designated  above  as  a  '  pseudo-hydrotheca ' 
is  of  considerable  morphological  interest,  for  it  may  throw  light  on  the 
origin  of  the  hydrotheca.  The  extension  of  the  chitinous  perisarc  of 
the  stem  over  the  body  of  the  hydranth  appears  to  be  attached  to  the 
latter.  A  true  hydrotheca  would  be  formed  if  the  perisarc  around  the 
hydranth  body  should  become  thicker  and  detached. 

Family  EUDENDRID.^. 

Tropkosome. — Colony  branching.  Hydranths  with  a  single  whorl 
of  filiform  tentacles  and  a  trumpet-shaped  or  hemispherical  proboscis 
which  is  expanded  distally  and  contracted  proximally,  thus  being 
sharply  distinguished  from  the  hydranth  body. 

Gonosome. — Reproductive  elements  developed  in  fixed  sporosacs  at- 
tached to  a  usually  more  or  less  degenerated  hydranth  body  below  the 
tentacles. 

This  family  contains  but  one  genus,  Eudendrium^  which  needs  no 
further  definition. 

EUDENDRIUM  VAGINATUM  Allman. 

(Plate  *v,  figs.  3-6.) 

Eudendrium  vaginatum  Allman,  Annals  and  Mag.   Nat.  Hist.,  Third  Se- 
ries, Vol.  XI,  p.  10,  Jan.,  1863. 

As  the  gonosome  of  this  species  has  not  heretofore  been  described, 
the  following  is  inserted  here  : 

Gonosome. — Gonophores  (female)  in  dense  clusters  around  the 
bodies  of  hydranths  that  are  usually  devoid  of  tentacles.     Each  go  no- 


l86  NUTTING  [l68] 

phore  is  borne  on  a  pedicel  which  resembles  those  of  Garveia^  having 
a  distinct  expanded  collar  a  short  distance  below  the  hydranth. 

Distribution. — Sitka  Harbor  and  Yakutat,  Alaska,  abundant  (Harri- 
man  Expedition)  ;   Shetland  Island,  Scotland  (Allman). 

This  beautiful  species  bears  considerable  resemblance  to  Euden- 
drium  annulatum  Allman,  especially  in  its  gonosome  which  Allman 
describes  as  follows  :  ' '  The  gonophores  are  grouped  in  clusters,  con- 
sisting of  from  eight  to  twenty  egg-shaped  bodies  attached  around  the 
axis  of  gonoblastidea,  which  are  of  moderate  length."^ 

Were  it  not  for  a  peculiar  character  of  the  trophosome,  i.  e.,  the  ex- 
panded pseudo-hydrotheca  investing  the  body  below  the  tentacles  much 
as  in  Garveia,  there  might  be  some  suspicion  that  JS.  vaginatum  and 
E.  annulatum  are  synonyms,  particularly  in  view  of  the  fact  that  both 
were  described  from  the  Shetland  Islands. 

It  also  seems  not  improbable  that  Eudendrium  Pygmceum  Clark  * 
may  be  another  synonym  of  E.  vaginatum.,  as  Clark's  description  of 
the  gonosome  agrees  well  with  the  gonosome  described  above.  If 
this  be  true,  it  is  also  likely  that  the  dried  stems  described  by  Clark 
from  Santa  Cruz,  California,  will  be  found  to  belong  to  this  same 
species. 

Family  TUBULARID^E, 

Trophosome. — Hydranths  large,  with  a  basal  whorl  of  filiform  ten- 
tacles and  a  distal  set  of  closely  crowded  shorter  filiform  tentacles. 

Gonosome. — Reproductive  elements  developed  in  sessile  medusae 
borne  in  clusters  just  above  the  basal  tentacles  and  producing  actinules 
instead  of  planulae. 

TUBULARIA. 

The  only  genus  included  in  the  family  in  the  sense  here  used. 

TUBULARIA  HARRIMANI  sp.  nov. 
( Plate  JSH.) 

Trophosome. — Stem  usually  unbranched,  attaining  a  height  of  i  ^ 
inches,  irregularly  and  sparingly  annulated  and  increasing  in  size  from 
the  proximal  to  the  distal  end,  but  more  rapidly  on  the  basal  portion ; 
a  marked  constriction  some  distance  below  the  hydranth  body ;  stem 
canaliculated  between  the  constriction  and  the  hydranth.  Hydranth 
with  forty  to  fifty  basal  tentacles  and  about  twenty  in  the  distal  set. 

Gonosome. — Gonophores  borne  in  about  twelve  very  long  and 
densely  crowded  racemes,  which  are  supported  by  long,  tentacle-like 

'Ann.  and  Mag.  Nat.  Hist.,  3d  Series,  Vol.  xiii,  p.  83,  Jan..  1864. 
*Proc.  Acad.  Nat.  Sciences,  Philadelphia,  p.  232,  1876. 


[169]  THE    HYDROIDS  187 

pedicels  arising  above  the  proximal  row  of  tentacles.  Gonophores  (fe- 
male) with  three  to  five  long  tentacular  processes  which  are  sometimes 
half  the  length  of  the  gonophore.  The  actinule  at  birth  is  without  a 
distal  row  of  tentacles,  and  the  gonophore  has  no  indication  of  radial 
canals. 

Distribution. — Orca,  Prince  William  Sound,  Alaska  (W.  E.  Ritter). 

Exclusive  of  this  species  there  have  now  been  described  four  species 
of  Tubularia  from  the  Pacific  Coast  of  North  America;  Parypha 
microcephala  (A.  Agassiz),^  which  differs  from  the  present  species  in 
having  flattened,  instead  of  round,  tentacular  processes  to  the  gono- 
phores ;  Tubularia  elegans  Clark,*  which  has  mere  tubercles  instead 
of  the  filiform  processes  to  the  gonophores ;  Tubularia  borealis 
Clark,'  which  differs  in  having  laterally  compressed  processes  to  the 
gonophores;  and  Tubularia  larynx  Ellis  and  Solander*  (reported  by 
Gary  S.  Calkins),  which  differs  from  T.  harrimani  in  the  number  of 
both  proximal  and  distal  sets  of  tentacles,  as  well  as  in  several  other 
characters. 

The  species  seems  to  be  abundant  at  Orca,  as  numerous  specimens 
were  found. 

CAL  TPTBR  OB  LAS  TEA. 

Hydroida  in  which  hydrothecae  are  developed  for  the  protection  of 
the  hydranths  and  gonangia  for  the  protection  of  the  gonophores. 

Family   CAMPANULARID^^. 

Trofhosome. — Hydrothecae  well  developed,  non-operculate,  never 
adnate  nor  immersed  in  the  stem  and  always  with  a  septum  partially 
dividing  the  hydrothecal  cavity  from  the  stem  cavity.  Hydranths 
usually  with  conical  proboscis  and  a  single  whorl  of  filiform  tentacles. 

Gonosome. — Gonophores  producing  planulae  or  free  medusae. 

It  would  be  hard  to  find  two  authorities  who  would  agree  as  to  the 
genera  of  this  exceedingly  perplexing  family.  The  arrangement  here 
adopted  is  substantially  the  same  as  that  used  by  the  writer  in  another 
work  now  in  press."  It  is  not  offered  as  a  final  solution  of  the  diffi- 
culty, but  as  a  convenience  in  discussing  the  group  in  the  present 
connection. 

'  North  American  Acalephae,  p.  195. 
^Transactions  Conn.  Acad.  Sci.,  Vol.  in,  p.  253,  1876. 
'Proc.  Acad.  Nat.  Sci.  Philadelphia,  p.  231,  1876. 
<Proc.  Boston  Soc.  Nat.  Hist.,  Vol.  xxviii.  No.  13,  p.  335. 
*  Handbook  of  the  Hydroids  of  the  Woods  Hole  Region.     To  be  published  by 
the  U.  S.  Fish  Commission. 


1 88  NUTTING  [^70] 

CLYTIA. 

Trophosome. — Stem  not  regularly  branched.  Hydrothecae  with 
toothed  margins,  or  with  excessively  thick  walls  and  with  long 
pedicels. 

Gonosome. — Reproduction  by  means  of  free  medusae. 

CLYTIA  CALICULATA  (Hincks). 

(Plate-aewH,  figs,  i,  2.) 

Campanularia  caliculata  Hincks,  Annals  and  Mag.  Nat.  Hist.,  2nd  ser.,  Vol. 
XI,  p.  178,  March,  1853. — Verrill,  Preliminary  check-list  of  Marine 
Invertebrates  of  Atlantic  Coast,  etc.,  p.  16,  1879. — Marktanner-Turn- 
ERETSCHER,  Hydroiden  von  Ost-Spitzbergen,  Zool.  Jahrb.,  Vol.  viii,  p. 
406.  1895. — Calkins,  Some  Hydroids  from  Puget  Sound,  Proc.  Boston 
Soc.  Nat.  Hist.,  Vol.  xxviii,  No.  13,  p.  351,  1899. 

Some  authors,  as  Levinsen,  regard  this  species  as  identical  with 
C  Integra  Macgillivray.  The  mode  of  reproduction  is  so  different, 
however,  that  the  two  would  go  into  different  genera  in  the  classifica- 
tion here  adopted. 

Distribution. — ^Yakutat,  Alaska  (HarrimanExped.)  ;  British  Coast 
(Hincks)  ;  Spitzbergen  (Marktanner-Turneretscher)  ;  New  England 
Coast  (Verrill)  ;   Puget  Sound  (Calkins) . 

CLYTIA  COMPRESSA  (Clark). 
(Plate-aesHH,  figs.  3,  4.) 

Campanularia  compressa  Clark,  Proc.  Acad.  Nat.  Sciences,  Philadelphia, 

p.  214,  1876. 
Eticopella  campanularia  (VON  Lendenfeld)?  Uber  Coelenteraten  der  Sudsee, 

IV,  Mitth.  Zeitsch,  Wiss.  Zool.,  xxxviii,  p.  497,  1883. 

Distribution. — Orca,  Alaska  (Harriman  Exped.)  ;  Shumagin 
Islands  (Clark) .  The  figures  given  of  this  species  well  illustrate  the 
great  variation  in  thickness  of  the  hydrothecal  walls.  All  the  speci- 
mens thus  far  discovered  were  found  attached  to  Laminaria,  over 
which  they  creep  in  great  profusion. 

Von  Lendenfeld  makes  his  Eucopella  campanularia  the  subject  of 
one  of  his  masterly  monographic  papers  and  it  appears  to  agree  in 
every  particular  with  the  species  under  discussion.  If  I  am  correct  in 
supposing  the  two  species  identical,  the  name  Eucopella  companularia 
will  become  a  synonym  and  a  very  exceptional  distribution  will  be  re- 
corded for  Clytia  compressa.  It  is  interesting  to  note  that  von 
Lendenfeld's  species  was  also  found  growing  on  Laminaria. 

The  present  writer  does  not  agree  with  Calkins  in  his  suggestion 
that  C.  compressa  is  a  synonym  of  C.  caliculata. 


[171]  THE    HYDROIDS  189 

CAMPANULARIA. 

Trofhosome. — Colony  unbranched  or  regularly  branched ;  stem 
simple  or  fascicled ;  hydrothecae  campanulate,  never  completely  ses- 
sile nor  with  operculum. 

Gonosome. — Gonophores  producing  planulae  without  the  interven- 
tion of  medusae. 

CAMPANULARIA  VERTICILLATA  (Linn.) 

Sertularia  verticillata  Linn.,  Syst.  Nat.,  loth  ed.,  p.  811,  1758. 
Campanularia  verticillata  Sars,  Bidrag  til  Kundskaben  om  Norges  Hydroider, 

p.  46,   1873. — ^Verrill,    Preliminary  check -list  of  Marine  Invertebrates 

of  Atlantic  Coast,  p.  16,  1879. 

Distribution. — Kadiak,  Alaska  (Harriman  Exped.)  ;  North  Cape, 
Norway  (Sars)  ;  New  England  Coast  (Verrill). 

CAMPANULARIA  DENTICULATA  Clark. 

Campanularia  denticulata  Clark,  Proc.  Acad.  Nat.  Sciences,  Philadelphia, 
p.  213,  1876. 

Distribution. — Orca,  Alaska  (Harriman  Exped.);    Port  Etches, 

Alaska  (Clark). 

CAMPANULARIA  LINEATA  Nutting. 

Campanularia  lineata  Nutting,  Hydroida  from  Alaska  and  Puget  Sound, 
Proc.  U.  S.  Nat.  Mus.,  Vol.  xxi,  p.  744,  1899. 

Distribution. — Berg  Inlet,  Glacier  Bay,  Alaska  (Harriman  Ex- 
ped.) ;  Puget  Sound  (Nutting). 

CAMPANULARIA  RITTERI  sp.  nov. 
(PlatJ^^,  fig.5.) 

Tropkosome. — Colony  usually  consisting  of  unbranched  pedicels 
growing  directly  from  a  creeping  rootstock.  Pedicels  long  and 
slender,  usually  with  a  single  distinct  annulation  at  the  distal  end  just 
below  the  hydrotheca  and  about  three  less  distinct  ones  at  the  proximal 
end,  the  middle  portion  not  being  annulated.  Hydrothecae  cylindrical, 
large,  delicate  in  structure  and  with  a  perfectly  even  rim. 

Gonosome. — Unknown. 

Distribution. — Juneau,  Alaska,  20  fathoms.  Collected  by  Prof. 
\Vm.  E.  Ritter  to  whose  efforts  the  fine  series  of  Hydroids  here  dis- 
cussed is  so  largely  due,  and  for  whom  this  species  is  named. 

CAMPAI^LARIA  SPECIOSA  Clark. 
(PIate«aB»,  fig.  3,  Plate  sax,  fig.  3.) 
Campanularia  speciosa  Clark,   Proc.  Acad.  Nat.  Sciences,  Philadelphia,  p. 
214,  1876. — Levinsen,  Meduser,   Ctenophorer  eg  Hydroider  fra  Gron- 
lands  Vestkyst,  p.  25,  1893. 


IpO  NUTTING  [172] 

Campanularia  crenata  Allman,  Diagnoses  of  new  Genera  and  Species  of 
Hydroida,  Linnaean  Society  Journal,  Zoology,  Vol.  xi,  p.  258,  1876. 

Distribution. — Orca,  Alaska  (Harriman  Exped.)  ;  Yukon  Harbor, 
Big  Koniuji,  Shumagin  Islands,  Alaska  (Clark)  ;  Japan  Coast  (All- 
man)  ;  Greenland  (Levinsen) . 

CAMPANULARIAURCEOLATA  Clark. 

(Plate  4b»,  fig.  2.) 

Campanularia  urceolata   Clark,  Proc.  Acad.  Nat.   Sciences,  Philadelphia, 
p.  215,  1876. 

Distribution. — Yakutat  Bay,  Alaska  (Harriman  Exped.)  ;  Lituya 
Bay,  Alaska  (Clark) . 

The  specimens  collected  by  the  Harriman  Expedition  were  growing 
profusely  over  the  stems  and  branches  of  Thuiaria  costata  in  com- 
pany with  another  parasitic  species. 

CAMPANULARIA  ^DUPLICATA  sp.  nov. 
( Plate -rtHf;  fig.  1.) 

Tropkosome. — Colony  consisting  of  unbranched  stems  or  pedicels 
springing  from  a  creeping  rootstock.  Pedicels  one  to  three  times  as 
long  as  the  hydrothecae,  and  strongly  annulated  throughout.  Hydro- 
thecae  deeply  campanulate,  thick-walled ;  margins  armed  with  twelve 
to  fourteen  rather  pointed  teeth,  and  reduplicated  once  or  twice,  giving 
a  striking  and  unusually  ornate  appearance. 

Gonosome. — Gonangia  roughly  ovate,  irregular  in  outline,  with  a 
short  neck,  small  terminal  aperture  and  a  very  short  pedicel.  They 
were  empty  in  the  specimens  examined,  so  that  it  was  impossible  to 
ascertain  whether  they  produced  planulae  or  medusae. 

Distribution.  —  Yakutat,  Alaska  (Harriman  Exped.).  All  the 
specimens  were  found  growing  in  a  parasitic  manner  over  colonies  of 
Thuiaria  costata.,  in  company  with  Campanularia  urceolata.  The 
two  species  were  often  so  intimately  interwoven  as  they  crept  over  the 
stems  and  branches  of  the  sertularian  that  I,  at  first,  thought  them 
dimorphic  forms  of  one  species.  However,  in  all  cases  careful  dissection 
showed  that  they  were  entirely  separate  colonies.  The  reduplication 
of  the  hydrothecal  margins  seems  to  be  a  constant  feature  and  adds 
peculiar  beauty  to  this  striking  little  campanularian. 

CAMPANULimA  REGIA  sp.  nov. 

(Plate  «»i  figs.  I,  2.) 
Tropkosome. — Colony  consisting  of   a  creeping  rootstock  without 
annulations,  giving  forth  strong  pedicels  that   are  sometimes  longer 


[173]  THE    HYDROIDS  I9I 

than  the  hydrothecae  and  sometimes  considerably  shorter,  without  a 
definite  swelling  below  the  hydrothecag.  Hydrothecae  immense,  in 
one  case  nearly  ^  of  an  inch  in  height,  long,  tubular-urceolate,  ex- 
panded distally,  with  slightly  everted  and  broadly  sinuous  margin. 
The  margin  is  reduplicated  in  one  specimen.  Hydranth  with  about 
twenty  tentacles. 

Gonosome. — Not  known. 

Distribution. — Orca,  Prince  William  Sound,  Alaska  (W.  R.  Coe, 
Harriman  Exped.) . 

This  species  is  closely  allied  to  C.  grandis  Allman,^  and  may  be 
identical  with  it  although  it  differs  from  AUman's  description  in  the 
character  of  the  pedicels  which  he  describes  as  having  distinct  node- 
like enlargements  immediately  below  the  hydrothecae.  The  hydro- 
thecae are  larger  than  those  of  any  other  campanularian  known  to  me. 
But  one  small  colony  was  found  and  it  was  creeping  over  another 
hydroid. 

OBELIA. 

Trophosome. — Colony  regularly  branching ;  stem  simple  or  com- 
pound. Hydrothecae  campanulate,  thin,  never  with  greatly  thickened 
walls. 

Gonosome. — Reproduction  by  means  of  medusae  which  are  disk- 
shaped,  with  four  radial  canals,  more  than  eight  marginal  tentacles, 
eight  interradial  lithocysts  and  a  short  manubrium  without  mouth  ten- 
tacles. 

OBELIA  DICHOTOMA  (Linn.). 

Sertularia  dichototna  Linn.,  Systema  Naturae,  Ed.  x,  p.  812.  1758. 

Obelia  dichotoma  Schulze,  Nordsee  Expedition,  Hydroida,  p.  129,  1872. — 
Verrill,  Preliminary  check-list  Marine  Invertebrates  of  Atlantic  coast, 
p.  16,  1879. — Calkins,  Some  Hydroids  from  Puget  Sound,  Proc.  Boston 
Soc.  Nat.  Hist.,  Vol.  xxviii.  No.  13,  p.  256,  1899. 

Distribution. — Sitka,  Berg  Inlet,  and  Orca,  Alaska  (Harriman 
Exped.)  ;  British  Coast  (Hincks)  ;  Helgoland  (Schulze)  ;  Puget 
Sound  (Calkins). 

OBELIA  PLICATA  Hincks. 

Obelia  plicata  HiNCKS,  British  Hydroid  Zoophytes,  p.  159,  1868. — Nutting, 
Hydroida  from  Alaska  and  Puget  Sound,  Proc.  U.  S,  Nat.  Mus.,  Vol. 
xxi,  No.  13,  p.  741,  1899. 

Distribution. — Orca,  Alaska  (Harriman  Exped.)  ;  Puget  Sound 
(Nutting)  ;  British  Coasts  (Hincks) . 

'  Diagnoses  of  new  Genera  and  Species  of  Hydroida ;  Linnsean  Soc.  Jour. 
Zoology,  Vol.  XI,  p.  259. 


192  NUTTING  [174] 

OBELIA  BOREALIS  sp.  nov. 
:srn 
(Plate 3ffis^  figs.  4,  6.) 

Trophosome. — Colony  sometimes  attaining  a  height  of  eighteen 
inches,  but  usually  much  shorter ;  stem  not  truly  fascicled,  although 
several  stems  may  be  interwoven,  exceedingly  long  and  slender,  sinu- 
ous, giving  off  lateral  branches  in  pairs  on  proximal  portion  and  more 
often  singly  on  distal  portion ;  branches  w^ith  a  strong  tendency  to  ver- 
ticillate  arrangement,  forming  oblique  angles  vv^ith  the  stem  and 
divided  into  numerous  branchlets  in  a  flabellate  manner.  Pedicels 
short  and  completely  annulated,  or  long  and  annulated  only  at  ends, 
set  on  broad  shoulders  of  the  stem.  Hydrothecse  funnel-shaped,  the 
sides  usually  straight,  aperture  writh  an  even  rim.  Hydranths  not  well 
preserved  in  specimens  examined. 

Gonosome. — Gonangia  borne  in  axils  of  branches  and  branchlets, 
oblong-ovate,  truncated  above,  having  a  collar  in  mature  specimens ; 
aperture  apparently  very  large,  pedicels  strongly  annulated.  The 
gonangia  of  the  specimens  examined  were  filled  with  developing 
medusae  of  the  regular  Obelia  type. 

Distribution. — Yakutat,  Alaska  (Harriman  Exped.). 

This  fine  species  is  related  to  O.  Jlabellata,  but  the  hydrothecae  are 
much  deeper  than  in  O.Jlabellata,  in  which  they  are  sub-triangular  in 
outline.  It  also  bears  some  resemblance  to  O.  commissuralis,  which, 
however,  is  a  much  more  delicate  species,  with  smaller  and  more 
campanulate  hydrothecae. 

OBELIA  DUBIA  sp.  nov. 
(Plate seat,  fig.  i.) 

Trophosome. — Colony  attaining  a  height  of  about  %  inch;  stem 
sparingly  branched,  the  main  stem  and  larger  branches  sinuous  or 
slightly  geniculate,  giving  forth  pedicels  singly  or  in  opposite  pairs  at 
the  bends.  Pedicels  rather  long  and  annulated  throughout,  the  stem 
also  more  extensively  annulated  than  in  most  species  of  the  genus. 
Hydrothecae  very  large,  deep,  tubular,  with  very  shallow  undulations 
around  the  margin,  from  between  which  lines  run  down  for  a  short 
distance  on  the  surface  of  the  hydrothecae. 

Gonosome. — Unknown. 

Distribution. — Orca,  Alaska  (Harriman  Exped.). 

This  species  bears  some  resemblance  to  O.  bidentata  Clark,  found 
on  the  New  England  Coast,  but  differs  in  the  nature  of  the  hydrothe- 
cal  teeth  which  are  mere  sinuosities,  instead  of  being  mucronate  with 
two  denticles  each  as  in  the  latter  species. 


[l75]  THE    HYDROIDS  I93 

HEBELLA. 

Tropkosome. — Pedicels  arising  from  a  creeping  rootstock,  very 
short.  Hydrothecae  tubular,  with  entire  margins,  without  opercula, 
and  having  their  cavities  separated  from  those  of  the  stems  by  a  partial 
septum.     Hydranths  with  a  conical  proboscis. 

This  genus  was  originally  instituted  by  Allman.^  As  here  defined 
it  includes  several  species  heretofore  included  in  the  genus  Lafcea. 

HEBELLA  POCILLUM  (Hincks). 

Lafcea  pocillum  Hincks,  British  Hydroid  Zoophytes,  p.  204,  1868. — Clark, 
Proc.  Acad.  Nat.  Sciences,  Philadelphia,  p.  215,  1876. — Verrill,  Pre- 
liminary check-list  Marine  Vertebrates  of  Atlantic  coast,  p.  17,  1879. — 
Bergh,  Goplepolyper  (Hydroider)  fra  Kara-Havet,  p.  333,  1887. 

Distribution. — Kadiak,  Alaska  (Harriman  Exped.)  ;  Nunivak 
Island,  Alaska  (Clark)  ;  Kara  Sea  (Bergh)  ;  British  Coasts  (Hincks)  ; 
New  England  Coast  (Verrill). 

GONOTHYRffiA. 

Trofhosome. — Much  as  in  Obelia. 

Gonosome. — Planulae  produced  in  sessile  medusaform  gonophores 
which  remain  attached  to  the  top  of  the  gonangia  until  the  spermatozoa 
or  planulae  are  discharged. 

GONOTHYIL^A  INORNATA  sp.  nov. 
(Plate  IBC,  figs.  2-4.) 

Trophosome. — Colony  attaining  a  height  of  about  two  inches  and 
consisting  of  a  main  stem  which  almost  immediately  breaks  up  into  a 
number  of  very  slender,  erect,  almost  straight  branches  which  are 
ornamented  with  about  three  annulations  immediately  above  the  origins 
of  the  pedicels.  Pedicels  alternate,  erect,  much  broader  below  than 
above  and  with  seven  to  ten  annulations.  Hydrothecae  funnel-shaped, 
with  entire  margins. 

Gonosome. — Gonangia  borne  in  the  axils  of  the  pedicels,  slender, 
obconic,  with  a  tendency  to  annulation.  Each  gonangium  contains  a 
single  sporosac  which  when  mature  rests  upon  the  summit  of  the  go- 
nangium and  has  little  indication  of  radial  canals  or  tentacles. 

Distribution. — Yakutat  Bay,  Alaska  (Harriman  Exped.). 

This  species  differs  from  others  of  the  genus  in  having  but  one 
sporosac  to  each  gonangium  and  in  the  obliteration  of  most  of  the 
medusoid  characters  of  the  sporosac.  The  entire  margin  of  the  hydro- 
theca  is  also  an  exceptional  character. 

^Allman,  Challenger  Report,  Hydroida,  Second  Part,  p.  29,  1888. 


'94  NUTTING  [176] 

Family   CAMPANULINlDyE. 

Trophosome. — Colonies  branched  or  unbranched.  Hydrothecae 
borne  on  pedicels,  tubular,  ending  in  an  operculum  composed  of 
several  converging  segments  or  triangular  flaps.  Hydranth  with  a 
conical  proboscis. 

Gonosome. — Gonangia  producing  free  medusae  or.  planulae. 

CAMPANULINA. 

Trophosome. — Hydrothecae  thin-walled,  the  upper  portion  cleft  so 
as  to  produce  very  long  and  slender  teeth  which  form  an  operculum  by 
the  convergence  of  their  free  ends. 

Gonosome. — Gonangia  producing  bell-shaped  medusae,  with  four 
radial  canals,  two  or  four  marginal  tentacles,  and  eight  lithocysts. 

CAMPANULINA  RUGOSA  sp.  nov. 
(Plate  XXII,  figs.  1,2.) 

Trophosome. — Colony  attaining  a  height  of  about  J^  inch.  Stem 
irregularly  branched ;  branches  tending  to  an  alternate  arrangement, 
straggling,  geniculate  ;  stem  and  branches  strongly  and  regularly  annu- 
lated  throughout.  Pedicels  very  short,  with  three  to  six  annulations. 
Hydrothecae  ovoid-oblong,  the  distal  third  being  composed  of  the  oper- 
culum consisting  of  ten  or  twelve  segments.  The  hydranths  have  about 
sixteen  tentacles. 

Gonosome. — Gonangia  in  axils  of  the  pedicels  and  branches,  some- 
times aggregated  on  certain  branches  to  the  exclusion  of  hydrothecae. 
They  are  oblong-ovoid  in  shape  and  somewhat  flattened  on  their  distal 
ends.     Each  gonangium  contains  a  single  medusa  when  mature. 

Distribution. — Juneau,  Alaska  (Harriman  Exped.).  The  speci- 
mens were  found  growing  on  Ohelia. 

CALYCELLA. 

Trophosome. — Stem  a  creeping  rootstock  sending  forth  short  an- 
nulated  pedicels.  Hydrothecae  tubular,  thick-walled,  with  opercula 
that  are  distinct  from  the  hydrothecal  teeth,  and  composed  of  several  tri- 
angular segments. 

Gonosome. — Gonangia  borne  on  the  rootstock,  and,  when  mature, 
bearing  acrocysts. 

CALYCELLA  SYRINGA  (Linn.). 

Sertularia  syringa  Linn.,    Systema   Naturae,  Ed.  xii,  Tom.  i,  Pars  11,  p, 
131X,  1767. 


[l77]  THE    HYDROIDS  195 

Calycella  syringa  Clark,  Proc.  Acad.  Nat.  Sciences,  Philadelphia,  p.  210, 
1876. — Verrill,  Preliminary  Check-list  Marine  Invertebrata  Atlantic 
Coast,  p.  17,  1879. — Bergh,  Goplepolyper  (Hydroider)  fra  Kara-Havet, 
p.  335,  1887. — Nutting,  Hydroida  from  Alaska  and  Puget  Sound,  Proc. 
U.  S.  Nat.  Mus.,  Vol.  xxi,  p.  741,  1899. 
Distribution. — Berg  Inlet  and  Kadiak,  Alaska  (Harriman  Exped.)  ; 

Coal  Harbor,  Shumagin  Islands,  Alaska  (Clark)  ;  Kara  Sea  (Bergh)  ; 

British    Coasts    (Hincks) ;    New   England   Coast    (Verrill) ;    Puget 

Sound  (Nutting). 

Family  LAFCEIDyE. 

Trophosome. — Hydrothecae  tubular,  margins  without  teeth  or  oper- 
cula,  the  hydrothecal  cavity  not  divided  from  the  stem  cavity  by  a  par- 
tial septum.  "^ 

Gonosome. — Gonangia  forming  a  '  Coppinia  '  mass. 

LAFCEA. 

Trophosome. — Colony  with  a  fascicled  stem,  and  with  hydrothecae 
either  free  or  partially  immersed  in  the  stem,  the  distal  portion  not  be- 
ing abruptly  turned  upward. 

Gonosome. — A  '  Coppinia '  mass. 

LAFCEA  DUMOSA  (Fleming). 

Sertularia  dumosa  Fleming,  Edinburgh  Phil,  Jour.,  11,  p.  83,  1828. 

Lafoea  dumosa  Sars,  Bidrag  til  Kundskaben  om  Norges  Hydroider,  p.  45, 
1873. — Clark,  Proc.  Acad.  Nat.  Sciences,  Philadelphia,  p.  210,  1876. — 
Verrill,  Preliminary  Check-list  Marine  Invertebrates  of  Atlantic  Coast, 
p.  17,  1879. — Nutting,  Hydroida  from  Alaska  and  Puget  Sound,  Proc. 
U.  S.  Nat.  Mus.,  Vol.  xxi,  p.  741,  1899. 

Distribution. — Dutch  Harbor,  Unalaska  (Harriman  Exped.)  ;  Port 

Etches,  Alaska  (Clark)  ;  North  Cape,  Norway  (Sars)  ;  British  Coast 

(Hincks)  ;  New  England  Coast  (Verrill)  ;  Puget  Sound  (Nutting)  ; 

California  Coast  (Clark). 

LAFCEA  GRACILLIMA  (Alder). 

Campanularia  gracillima  Alder,  Catalogue  Zoophytes  of  Northumberland 
and  Durham,  Trans.  Tyneside  Naturalists'  Field  Club,  p.  39,  1857. 

Lafcea  gracillima  Clark,  Proc.  Acad.  Nat.  Sciences,  Philadelphia,  p.  216, 
1876. — Verrill,  Preliminary  Check-list  Marine  Invertebrates  of  Atlantic 
Coast,  p.  17,  1879. — Marktanner-Turneretscher,  Hydroiden  von 
Ost-Spitzbergen,  Zoolog.  Jahrbuch.,  Vol.  viii,  p.  4x0,  1895. — Nutting, 
Hydroida  from  Alaska  and  Puget  Sound,  Proc.  U.  S.  Nat.  Mus.,  Vol.  xxi, 
p.  741.  1899. 

Distribution. — Juneau,  Berg  Inlet  and  Orca,  Alaska  (Harriman 
Exped.)  ;  Shumagin  Islands,  Alaska  (Clark)  ;  British  Coast  (Alder)  ; 


196  NUTTING  [178] 

Spitzbergen  (Marktanner-Turneretscher)  ;  New  England  Coast  (Ver- 
rill)  ;  Puget  Sound  (Nutting). 

LAFCEA  FRUTICOSA  M.  Sars. 

Lafoea  fruHcosa  M.  Sars,  Bemaerkninger  over  4  norske  Hydroider  Vid.  Selsk. 
Forh,,  1862. — G.  O.  Sars,  Bidragtil  Kundskaben  om  Norges  Hydroider, 
p.  26,  1873. — Clark,  Proc.  Acad.  Nat.  Sciences,  Phila.,  p.  216,  1876. 

Distribution. — Juneau,  Berg  Inlet  and  Kadiak,  Alaska  (Harriman 

Exped.)  ;  KIska  Harbor,  Shumagin  Islands,  Alaska  (Clark)  ;  British 

Coasts    (Hincks)  ;    Lofoten,  Norway  (G.  O.   Sars)  ;  New  England 

Coast  (Verrill)  ;  Puget  Sound  (Nutting,  MSS.). 

LAFCEA  ADHERENS  sp.  nov. 
(Plate  x»i  figs.  3,  4.) 

Trophosotne. — Colony  forming  an  encrusting  mass  of  adherent  root- 
stocks  disposed  both  longitudinally  and  transversely  over  colonies  of 
other  Hydroids,  the  tubes  of  the  rootstock  interwoven  much  like  the 
threads  of  a  fabric.  Hydrothecas  sessile,  tubular,  often  more  or  less 
curved,  aperture  facing  upward,  entire ;  margin  slightly  expanded. 
The  hydrothecae  are  very  irregularly  disposed,  being  much  more 
crowded  in  some  places  than  in  others. 

Gonosome. — The  '  Coppinia '  mass  is  much  like  that  of  Lafoea  du- 
mosa^  being  composed  of  closely  packed  gonangia  interspersed  with 
long,  tubular,  variously  curved  modified  hydrothecae.  The  gonangia 
are  flask-shaped,  with  a  tubular  neck  and  small  aperture.  Each 
gonanglum  apparently  contains  a  single  ovum. 

Distribution. — Kadiak  Harbor,  Alaska.  Growing  over  stems  of 
Thuiaria  turgida  (Harriman  Exped.). 

This  interesting  species  is  so  different  in  appearance  from  the  others  of 
the  genus  that  I  was  at  first  inclined  to  make  it  the  type  of  a  new  genus. 

GRAMMARIA. 

Trophosome. — Stem  fascicled,  composed  of  an  axial  tube  from 
which  the  hydrothecae  spring  and  to  which  they  are  partly  adnate, 
completely  enclosed  by  a  definite  number  of  peripheral  nonhydro- 
thecate  tubes. 

Gonosome. — A  '  Coppinia  *  mass. 

GRAMMARIA  IMMERSA  sp.  nov. 
(Plate  XXI,  figs.  5,  6.) 
Trophosome. — Stem   rigid,  erect,  giving  forth  scattered,  stitf  and 
straight,  alternate  branches  forming  nearly  a  right  angle  with  the  stem. 


[179]  THE    HYDROIDS  I97 

Height  of  a  fragmentary  specimen  about  ^  inch.  Stem  and  branches 
sharply  constricted  proximally,  composed  of  an  axial  tube  which  gives 
off  the  eight  or  nine  series  of  hydrothecae,  and  a  number  of  peripheral 
tiibes  enclosing  the  axial  tube  completely,  thus  burying  all  the  hydro- 
thecae nearly  to  their  distal  ends.  Hydrothecae  arranged  in  about  eight 
or  nine  longitudinal  series,  forming  spirals.  The  distal  ends  of  the 
hydrothecas  are  abruptly  bent  outward,  so  that  the  round,  even  aper- 
ture is  vertical.  When  the  peripheral  tubes  are  removed  the  hydro- 
thecae are  seen  to  be  long,  tubular,  doubly  curved,  narrowing  prox- 
imally, but  without  true  pedicels,  and  all  springing  from  the  axial  tube. 

Gonosome.  — Unknown . 

Distribution. — St.  Paul  harbor,  Kadiak  (Harriman  Exped.). 

FILELLUM. 

Trophosome. — Stem  a  creeping,  slender  rootstock,  parasitic  on 
'  other  hydroids,  often  forming  a  reticulate  structure.  Hydrothecae 
curved,  decumbent,  and  partly  adherent;  margin  entire,  without 
operculum. 

Gonosome. — A  'Coppinia'  mass. 

FILELLUM  SERPENS  (Hassell). 

Campanularia  serpens  Hassell,  Zoologist,  No.  69,  p.  2223. 

Filellum  serpens  Sars,  Bidrag  til  Kundskaben  om  Norges  Hydroider,  p.  29, 

1873. — Verrill,  Preliminary  Check -list  Marine  Invertebrates  of  Atlantic 

Coast,  p.  17,  1879. 

Distribution. — Juneau,  Alaska  (Harriman  Exped.)  ;    British  Coast 
(Hassell)  ;  Lofoten,  Norway  (Sars). 

Family  HALECJD^^. 
Trophosome. — Hydrothecae  reduced  to  the  form  of  saucer-shaped  or 
collar-like  hydrophores,  usually  borne  on  broad  tubular  pedicels ; 
margins  even,  often  reduplicated.  Hydranths  large,  incapable  of  re- 
tracting within  the  hydrophores,  and  with  a  conical  or  dome-shaped 
proboscis. 

Gonosome. — Gonangia  producing  planulae,  and  usually  differing  in 
the  two  sexes. 

HALECIUM. 
Trophosome. — No  specialized  defensive  'persons*  developed. 
Gonosome. — Female    gonangia    often    surmounted    by    a    pair    of 
hydranths. 

HALECIUM  HALECINUM  (Linn.). 
Sertularia  halecina  Linn.,  Systema  Naturae,  Ed.  x,  p.  809,  1758. 


198  NUTTING  [180] 

Halecium  halecinunt  Verrill,  Preliminary  Catalogue  Marine  Invertebrates 
Atlantic  Coast,  p.  17,  1879. — Marktanner-Turneretscher,  Hydroiden 
von  Ost-Spitzbergen,  p.  428,  1895. — Nutting,  Hydroida  from  Alaska 
and  Puget  Sound,  Proc.  U.  S.  Nat.  Mus.,  Vol.  xxi,  p.  741,  1899. 

Distribution. — Kadiak,  Alaska  (Harriman  Exped.)  ;  British  Coast 
(Hincks) ;  Greenland  (Marktanner-Turneretscher) ;  New  England 
Coast  (Verrill)  ;  Puget  Sound  (Nutting). 

HALECIUM  MURICATUM  (Ellis  and  Solander). 

Sertularia  muricata  Ellis  and  Solander,  Nat.  Hist.  Zoophytes,  p.  59,  1786. 

Halecium  muricatum  Verrill,  Preliminary  Check-list  Marine  Invertebrates 
Atlantic  Coast,  etc.,  p.  17,  1879. — Levinsen,  Meduser,  Ctenophorer  og 
Hydroider  fra  Gronlands  Vestkyst,  p.  61,  1893. — Clark,  Proc.  Acad. 
Nat.  Sci.,  Philadelphia,  p.  217,  1876. 

Distribution. — Orca,  Alaska  (Harriman  Expd.)  ;  British  Coasts 
(Ellis  and  Solander)  ;  Greenland  (Levinsen)  ;  New  England  Coast 
(Verrill). 

HALECIUM  SCUTUM  Clark. 

Halecium  scutum  Clark,  Proc.  Acad.  Nat.  Sci.,  Philadelphia,  p.  218,  1876. 
— BoNNEViE,  Norwegian  N.  Atlan.  Exped.,  p.  57,  1899. 

Distribution. — Berg  Inlet  and  Yakutat,  Alaska  (Harriman  Exped.)  ; 
Unalaska  (beach)  and  Shumagin  Islands,  Alaska  (Clark) ;  North 
Cape,  Norway  (Bonnevie). 

HALECIUM  REVERSUM  sp.  nov. 
(Plate  xxiii,  figs.  1,2.) 

Trophosome. — Colony  attaining  a  height  of  about  one  inch.  Main 
stem  fascicled,  branches  simple  and  alternate,  making  a  flabellate 
colony.  Nonfascicled  part  of  the  stem  and  branches  divided  into  inter- 
nodes,  each  of  which  bears  one  or  two  pedicels  springing  from  its 
proximal  portion.  Pedicels  long,  of  even  diameter  throughout,  often 
rugose  on  proximal  portion.  Hydrophores  with  large  everted  margins 
and  a  distinct  row  of  dots.  Reduplication  of  margins  distant,  when 
present.     Hydranth  small  for  this  genus,  with  about  twenty  tentacles. 

Gonosome. — Not  present  in  type  specimen. 

Distribution. — Juneau,  Alaska  (Harriman  Exped.). 

This  species  possesses  the  very  exceptional.  If  not  unique,  character 
of  having  the  pedicels  spring  from  the  proximal  part  of  the  Internode 
instead  of  the  distal  portion,  as  in  all  other  species  of  Halecium  with 
which  I  am  acquainted.  This  character  appears  to  be  constant.  The 
specimen  was  dredged  from  a  depth  of  twenty  fathoms. 


[l8l]  THB   HYDROIDS  1 99 

HALECIUM  ORNATUM  sp.  nov. 
(Plate  XXII,  figs.  3,4.) 

Trofhosome, — Colony  parasitic,  branching  irregularly.  Stems  not 
fascicled,  the  stem  and  branches  sparsely  and  irregularly  annulated. 
Pedicels  long,  of  equal  diameter  throughout.  Hydrophores  with  broad, 
everted  margins,  occasionally  reduplicated.  Hydranth  large,  with 
twenty-four  to  thirty  tentacles. 

Gonosome. — A  single  apparently  young  gonangium  was  borne  on  a 
pedicel  just  below  the  hydrophore.  It  was  in  form  a  truncated  and 
deeply  annulated  cone.  Probably  the  mature  gonangium  would 
resemble  that  found  in  the  next  species. 

Distribution. — Berg  Inlet,  Glacier  Bay,  Alaska.  Growing  on 
Lafcea  gracillima  (Harriman  Exped.). 


HALECIUM   SPECIOSUM  sp.  nov. 
(Plate  xxii,  figs.  1,2.) 

Trofhosome. — Colony  small,  attaining  a  height  of  about  Yz  inch. 
Stem  not  fascicled,  the  main  stem  and  branches  apparently  formed  of 
series  of  stout  pedicels,  each  giving  origin  to  another  pedicel  just  below 
the  hydrophore.  The  pedicels  thus  take  the  place  of  stem  joints, 
bending  alternately  to  the  right  and  left,  giving  a  geniculate  appearance 
to  the  series.  Pedicels  broad,  corrugated  proximally  and  smooth 
distally.  Hydrophores  large,  with  broadly  expanded  but  not  everted 
margins,  and  a  well  marked  row  of  dots.  There  appears  to  be  no  re- 
duplication of  the  margins.  Hydranths  very  large  with  twenty-four  to 
thirty  short  tentacles,  a  broad  oral  disk  occupied  by  the  low  dome- 
shaped  proboscis. 

Gonosome. — Gonangia  borne  on  rather  long  annulated  pedicels  be- 
low the  hydrophores,  particularly  on  the  upper  part  of  the  colony ; 
regularly  ovoid  in  outline,  and  evenly  and  beautifully  annulated 
throughout. 

Distribution. — Yakutat  Bay,  Alaska  (Harriman  Exped.). 

This  is  the  most  strikingly  ornamented  species  of  Ualecium  known 
to  the  writer.  Its  manner  of  growiih  is  exceptional,  although  not  un- 
known among  its  allies,  and  the  hydranth  is  more  like  the  polyp  of 
some  actinozoon  than  of  a  hydroid.  The  gonangia  are  beautiful  struc- 
tures. They  seemed  to  be  filled  with  a  granular,  ovoid  mass,  probably 
a  single  large  sporosac. 


200  NUTTING  [182] 

HALECIUM  ROBUSTUM  sp.  nov. 
(Plate  XXIII,  figs.  3,4,5.) 

Trophosome. — Stem  very  thick  and  fascicled,  consisting  of  an  im- 
mense number  of  wavy  tubes.  In  the  single  specimen  collected,  the 
main  stem  divides  near  its  base  into  three  heavy  fascicled  branches, 
which  themselves  branch  and  subdivide  extensively,  the  fasciculation 
continuing  nearly  to  the  tips  of  the  branches.  The  entire  height  of 
the  colony  is  about  three  inches.  The  branching  is  so  profuse  that  the 
arrangement  of  the  internodes  is  obscure.  The  ultimate  branches  give 
off  short  pedicels  and  sessile  hydrophores  in  what  appear  to  be  clusters 
or  whorls.  Pedicels  short,  tubular,  ending  in  an  exceedingly  shallow 
hydrophore.  Hydrophores  reduced  to  a  mere  narrow  rim,  marked  by 
the  internal  diaphragm  and  circlet  of  dots,  the  only  distinction  between 
pedicel  and  hydrophore,  as  the  margin  of  the  latter  is  not  appreciably 
everted.  Most  of  the  hydrophores  are  sessile,  being  set  on  mere 
shoulders  of  the  branch  from  which  they  grow.  The  circlet  of  dots 
can  only  be  made  out  with  great  difficulty  and  the  use  of  high  magnifi- 
cation. Hydranths  exceedingly  numerous  and  large,  covering  the 
branches  so  as  to  almost  entirely  conceal  them  from  view.  Tentacles 
about  twenty,  surrounding  a  low  conoid  proboscis. 

Gonosome. — Unknown. 

Distribution, — Berg  Inlet,  Glacier  Bay,  Alaska  (Harriman  Ex- 
ped.). 

This  species  bears  some  relation  to  Halecium  densum  Calkins,  *  but 
differs  from  that  species  in  the  hydrophores,  which  are  not  reduplicated 
and  have  straight,  not  everted,  margins.  The  hydranths  are  so  crowded 
that  a  branch  resembles  an  expanded  colony  of  Alcyonaria,  and  appears 
to  be  made  up  entirely  of  hydranths. 

Family  SERTULARID^^. 

Trophosome. — Hydrothecae  sessile,  more  or  less  adnate  by  their  side 
to  the  stem  and  branches  upon  which  they  grow;  always  in  more 
than  one  longitudinal  row  on  each  branch,  the  arrangement  usually 
biserial.     Hydranth  with  a  conical  proboscis. 

Gonosome. — Reproduction  always  by  means  of  planulae,  which  are 
developed  within  the  gonangia.     No  medusae. 

SERTULARELLA. 

Trophosome. — Stem  and  branches  divided  into  regular  internodes, 
each  bearing  one  or  two  hydrothecae ;  nodes  oblique.     Hydrothecae 
*Proc.  Boston  Soc.  Nat.  Hist.,  Vol.  28,  no.  13,  p.  343,  1899. 


[183]  THE   HYDROIDS  20I 

alternate,  borne  on  opposite  sides  of  the  stem  and  branches.  Margin 
usually  more  or  less  toothed,  aperture  usually  provided  with  an  oper- 
culum consisting  of  more  than  one  segment. 

SERTULARELLA  TRICUSPIDATA  (Alder). 

Sertularia  tricuspidata  Alder,  Catalogue  of  the  Zoophytes  of  Northumber- 
land and  Durham,  Trans.  Tyneside  Naturalists'  Field  Club,  p.  21,  1857. 

CotuUna  tricuspidata  A.  Agassiz,  North  American  Acalephae,  p.  146,  1864. 

Sertularella  tricuspidata  Clark,  Proc.  Acad.  Nat.  Sciences  Phila.,  p.  224, 
1876. — Marktanner-Turneretscher,  Hydroiden  von  Ost-Spitzbergen, 
p.  425,  1895. — NxjTTiNG,  Hydroida  from  Alaska  and  Puget  Sound,  Proc. 
U.  S.  Nat.  Mas.,  Vol.  xxi,  p.  741,  1899. 

Distribution. — ^Juneau,  Berg  Inlet,  and  Yakutat,  Alaska  (Harri- 
man  Exped.)  ;  Shumagin  Islands,  Semidi  Islands,  Unalaska,  Port 
Etches,  and  Kiska  Harbor,  Alaska  (Clark)  ;  British  Coast  (Alder)  ; 
New  England  Coast  (A.  Agassiz)  ;  Greenland  (Marktanner-Turner- 
etscher) ;  Puget  Sound  (Nutting) . 

SERTULARELLA  POLYZONIAS  (Linn.). 

Sertularia  poly zonias  Linn.,  Systema  Naturae,  Ed.  x,  p.  813,  1758. 
Sertularella  polyzonias  Gray,  List  of  the  Specimens  of  British  Animals  in  the 

British  Museum,  part  i,  Radiata,  London,  1847. — Sars,  Bidrag  til  Kunds- 

kaben  om  Norges  Hydroider,  p.  44,  1873. — Clark,  Proc.  Acad.  Nat.  Sci. 

Phila.,  p.  224,  1876. 
CotuUna  polyzonias  Agassiz,  Contributions  to  the  Natural  History  of  the  United 

States,  Vol.  iv,  p.  356,  1864. 
Sertularella  conica  Calkins,  Some  Hydroids  from  Puget  Sound,  Proc.  Boston 

Soc.  Nat.  Hist.,  VoL  xxviii,  p.  359,  1899. 

Distribution. — Orca,  Alaska  (Harriman  Exped.)  ;  Port  Etches  and 
Nunivak  Island,  Alaska  (Clark)  ;  British  Coasts  (Gray)  ;  North 
Cape,  Norway  (Sars)  ;  New  England  Coast  (Agassiz)  ;  Puget  Sound 
(Calkins) . 

Calkins,  in  the  reference  cited  above,  identifies  a  small  specimen 
otherwise  identical  with  S.  polyzonias.,  as  the  species  S.  conica  All- 
man,  and  says  :  "The  only  character,  and  that  a  small  one,  by  which 
to  distinguish  it  from  the  very  wide-spread  S.  polyzonias  is  the  well- 
marked  wrinkling  on  the  adcauline  side  of  the  hydrotheca."  Speci- 
mens from  Alaska  in  the  Harriman  Collection,  agreeing  with  Calkins's 
description  and  figures,  have  the  characteristic  gonosome  of  vS".  poly- 
zonias., and  I  therefore  consider  that  I  am  justified  in  regarding  his 
specimen  as  belonging  to  that  species. 

SERTULARELLA  SACCATA  sp.  nov. 
(Plate  XXIV,  figs.  1-3.) 
Sertularella  rugosa  Clark,  Proc.  Acad.  Nat.  Sci.  Phila.,  p.  224,  1876. 


202  NUTTING  [184] 

Sertulareila  geniculata  Marktanner-Turneretscher,  Die  Hydroiden  Des 
k.  k.  naturhistorischen  Hofmuseums,  p.  222,  1890. 

Trophosome. — Colony  consisting  of  a  sparingly  branched,  non- 
fascicled  stem  attaining  a  height  of  about  one  inch.  Stem  annulated 
and  nonhydrothecate  proximally,  otherwise  bearing  alternate  hydro- 
thecae,  one  to  each  internode ;  stems  and  branches  erect.  Hydrothecae 
roughly  ovate  in  general  outline,  with  a  laterally  inclined,  broad, 
smooth,  round  neck  or  collar  surmounted  by  a  four-toothed  aperture 
and  a  four-flapped  operculum ;  below  the  neck  the  body  of  the  hydro- 
theca  has  three  or  four  broad  annular  corrugations.  Hydranths  with 
about  sixteen  tentacles. 

Gonosome. — Gonangia  large,  oblong-ovate  in  general  outline,  with 
several,  seven  to  nine,  broad  annular  corrugations.  The  mature  ova 
are  enclosed  in  an  ovoid  acrocyst  resting  on  the  top  of  the  gonangium. 

Distribution. — Popof  Island,  Alaska  (Harriman  Exped.)  ;  Un- 
alaska,  Shumagin  Islands,  St.  Paul  Island  and  Nunivak  Island,  Alaska 
(Clark)  ;  Jan  Mayen  (Marktanner-Turneretscher). 

The  specimens  of  this  species  secured  by  the  Harriman  Expedition 
agree  well  with  the  figure  given  by  Clark  of  specimens  that  he  identi- 
fied as  S.  rugosa.  The  very  conspicuous  neck,  however,  would  seem 
to  be  sufficient  to  distinguish  S.  saccata  from  S.  rugosa.,  and  the  same 
difference  exists  between  the  gonangia  of  the  two  forms.  The  figure 
given  by  Marktanner-Turneretscher  for  vS".  geniculata  Hincks  differs 
greatly  from  Hincks's  original  description  and  figure,  and  agrees  well 
with  the  present  species,  except  that  the  hydrothecae  are  more  closely 
approximated  in  the  latter. 

THUIARIA. 

Trophosome. — Colony  branched,  the  branches  divided  into  unequal 
internodes,  each  bearing  several  pairs  of  opposite  or  subopposite  hy- 
drothecae. Hydrothecae  usually  deeply  immersed  in  the  stem  or  branch 
to  which  they  are  attached.  The  branches  are  alternate,  and  each 
springs  from  an  unpaired  hydrotheca. 

Gonosome. — ^Much  as  in  Sertularia. 

THUIARIA  ARGENTEA  (Ellis  and  Solander). 

Sertularia  argentea  Ellis  and  Solander,  The  Natural  History  of  many  curious 
and  uncommon  Zoophytes,  etc.,  p.  38,  1786. — Clark,  Hydroids  of  the 
Pacific  Coast  of  the  United  States  south  of  Vancouver  Island,  Trans. 
Conn.  Acad.,  Vol,  iii,  p.  251,  1876.— Verrill,  Preliminary  Check-list 
Marine  Invertebrates  Atlantic  Coast,  etc.,  p,  18,  1879. — Bergh,  Gople- 
polyper  (Hydroider)  fra  Kara-Havet,  p.  335,  1887. — Nutting.  Hydroida 
from  Alaska  and  Puget  Sound,  Proc.  U.  S.  Nat.  Mus.,  Vol.  xxi,  p.  741, 
1899. 


[l8s]  THE   HYDROIDS  203 

Distribution. — Yakutat,  Alaska  (Harriman  Exped.)  ;  British  Coast 
(Ellis  and  Solander)  ;  Kara  Sea  (Bergh)  ;  New  England  Coast  (Ver- 
rill)  ;  Puget  Sound  (Nutting)  ;  California  (Clark). 

THUIARIA  SIMILIS  (Clark). 
Sertularia  similis  Clark,  Proc.  Acad.  Nat.  Sci.  Phila.,  p.  219,  1876. 

Distribution. — Berg  Inlet,  Glacier  Bay,  Alaska  (Harriman  Exped.)  ; 
Hagmeister  Island,  Alaska  (Clark)  ;  Puget  Sound  (Nutting,  MSS.). 

THUIARIA  VARIABILIS  (Clark). 
Sertularia  variabilis  Clark,  Proc.  Acad.  Nat.  Sci.  Phila.,  p.  221,  1876. 

Distribution. — Orca,  Alaska  (Harriman  Exped.)  ;  numerous  sta- 
tions in  Alaska  (Clark)  ;  San  Miguel  Island,  California  (Clark)  ;  Puget 
Sound  (Nutting,  MSS.). 

THUIARIA  CUPRESSOIDES  (Clark). 
Sertularia  cupressoides  Clark,  Proc.  Acad.  Nat.  Sci.  Phila.,  p.  220,  1876. 

Distribution. — Yakutat,  Alaska  (Harriman  Exped.)  ;  Shumagin 
Islands  and  Port  MoUer,  Alaska  (Clark). 

THUIARIA  COEI  sp.  nov. 

(Plate  XXVI,  figs.  1-3.) 

Trophosome. — Colony  consisting  of  a  single  flexuous  stem  giving 
forth  regularly  alternate  branches.  Stem  three  inches  high,  and  divided 
into  irregular  internodes  each  bearing  a  branch  and  two  hydrothecae  on 
one  side  and  one  hydrotheca  on  the  other.  Branches  divided  into 
irregular  internodes,  each  usually  bearing  several  pairs  of  hydrothecae. 
Hydrothecae  subopposite,  turgid  basally,  narrowing  distally  to  a  hori- 
zontal aperture  which  is  pointed  on  its  outer  side.  An  upward  pro- 
jecting point  of  chitine  at  the  bottom  of  each  hydrotheca. 

Gonosome. — Gonangia  top-shaped,  or  obconical,  with  a  pronounced 
round  collar  and  rather  broad  aperture.  Proximal  portion  broadly  cor- 
rugated, and  narrowing  basally  to  a  short  curved  pedicel. 

Distribution.  —  Dutch  Harbor,  Alaska  (W.  R.  Coe,  Harriman 
Exped.). 

This  is  a  very  distinct  species,  and  the  top-shaped  gonangia  are 
quite  different  from  any  others  of  the  genus  that  I  have  seen. 

THUIARIA  FABRICII  (Levinsen). 

(Plate  XXIV,  figs.  4,  5.) 

Sertularia  fabricit  Levinsen,  Meduser,  Ctenophorer  eg  Hydroider  fra  Gron- 
lands  Vestkyst,  p.  48,  1893. — Calkins,  Some  Hydroida  from  Alaska  and 
Puget  Sound,  Proc.  Boston  Soc.  Nat.  Hist.,  Vol.  xxviii,  p.  361,  1899. 


204  NUTTING  [^86] 

Distribution, — Dutch  Harbor,  Alaska  (HarrimanExped.)  ;  Green- 
land (Levinsen)  ;  Puget  Sound  (Calkins) . 

A  specimen  in  the  Harriman  collection  agrees  perfectly  with  the 
descriptions  and  figures  of  both  Levinsen  and  Calkins.  I  have  directly 
compared  it  with  specimens  of  Sertularia  argentea  from  England, 
and  find  that  the  two  species  are  evidently  distinct,  T.  fabricii  differ- 
ing from  S.  argentea  in  the  following  particulars.  The  colony  is  much 
more  bushy  in  appearance,  and  more  compactly  branched.  The  hydro- 
thecae  are  more  nearly  in  pairs,  and  much  more  closely  approximated, 
are  more  densely  corneous  and  have  a  more  delicate  and  less  clearly 
defined  aperture.  The  gonangia  are  considerably  larger  and  of  thinner 
texture,  and  are  only  occasionally  armed  with  lateral  spines. 

It  should  be  explained  that  Levinsen  regards  his  Sertularia  fabricii 
as  identical  with  the  Sertularia  argentea  of  authors,  and  gives  it  the 
name  S.  fabricii.  My  opinion  is  that  the  species  is  distinct,  and  I 
recognize  the  name  given  by  him  because  he  has  correctly  described 
and  figured  the  species,  although  not  classing  it  as  distinct.  It  should, 
however,  be  placed  in  the  genus  Thuiaria^  for  it  comes  well  within 
that  genus  as  here  defined. 

THUIARIA  TURGIDA  Clark. 

(Plate  xjv,  figs.  4-6.) 

Thuiaria  turgida  Clark,  Proc.  Acad.  Nat.  Sci.  Phila,,  p.  229,  1876. — Nut- 
ting, Hydroida  from  Alaska  and  Puget  Sound,  Proc.  U.  S.  Nat.  Mus., 
Vol.  XXI,  p.  741,  1899. 

Distribution. — Sitka,  Orca,  Popof  Island,  and  Dutch  Harbor, 
Alaska  (Harriman  Exped.)  ;  Port  Etches,  Shumagin  Islands,  Semidi 
Islands,  and  many  other  points  in  Alaska  (Clark) . 

THUIARIA  GIGANTEA  Clark. 

Thuiaria gigantea  Clark,  Proc.  Acad.  Nat.  Sci.  Phila.,  p.  230,  1876 — Nut- 
ting, Hydroida  from  Alaska  and  Puget  Sound,  Proc.  U.  S.  Nat,  Mus., 
Vol.  xxi,  p.  741,  1899. 

Distribution.  —  Kadiak  and  Popof  Island,  Alaska  (Harriman 
Exped.)  ;  St.  Paul  Island,  Hagmeister  Island,  Unalaska  and  Kiska 
Harbor,  Alaska  (Clark)  ;  St.  Paul  Island  (Nutting) . 

THUIARIA  THUIARIOIDES  (Clark). 
Sertularia  thuiarioides  Clark,  Proc.  Acad.  Nat.  Sci.  Phila,,  p.  223,  1876. 

Distribution. — ^Yakutat,  Alaska  (Harriman  Exped.)  ;  Nunivak 
Island  and  Chignik  Bay,  Alaska  (Clark). 


[187]  THE   HYDROIDS  20$ 

THUIARIA  ELEGANS  sp.  nov. 
(Plate  XXV,  figs.  1-3.) 

Trofhosome. — Colony  consisting  of  a  central  nonfascicled  stem 
branching  in  a  plumose  manner  and  attaining  a  height  of  about  six 
inches.  Stem  bearing  hydrothecae  throughout  its  length,  divided  by 
oblique  nodes  into  long  and  irregular  internodes,  each  of  which  usually 
bears  three  or  four  branches ;  branches  alternate,  pinnately  arranged, 
unbranched  proximally,  and  distally  dividing  into  a  number  of  branch- 
lets;  internodes  of  stem  irregular,  but  each  bearing  normally  more 
than  one  pair  of  hydrothecae.  Hydrothecae  subalternate,  short,  pitcher- 
shaped,  with  a  double  curve  in  front  and  an  even  aperture  much  like 
the  top  of  a  pitcher ;  operculum  composed  of  a  single  flap. 

Gonosome. — Gonophores  borne  on  the  upper  sides  of  the  distal  ends 
of  the  branches  in  a  closely  set  double  row.  The  individual  gonangium 
is  slender,  oblong-oval,  with  a  truncated  top,  an  internal  distal  plug 
which  appears  as  a  dark  collar,  and  an  internal  mass  of  developing  sex 
elements. 

Distribution. — Berg  Inlet,  Glacier  Bay,  20  fathoms ;  Dutch  Har- 
bor, Alaska  (Harriman  Exped.). 

THUIARIA  COSTATA  sp.  nov. 
(Plate  xxvi,  figs.  4-9.) 

Trofhosome. — Colony  usually  a  single  stem  giving  forth  alternate 
branches,  the  whole  having  a  plumose  appearance,  stem  simple, 
straight,  the  lower  part  composed  of  regular  internodes,  each  bearing  a 
pair  of  subopposite  hydrothecae,  the  upper  part  divided  into  regular 
internodes,  each  bearing  a  branch  and  three  hydrothecae ;  nodes 
oblique.  Branches  alternate  and  themselves  branching  dichotomously, 
divided  into  unequal  internodes,  each  bearing  more  than  two  suboppo- 
site hydrothecae.  Hydrothecae  turgid  below  and  narrowing  above  into 
a  short  neck  which  ends  in  a  round  aperture  facing  upward.  A  chiti- 
nous  spine  projects  downward  from  the  lower  inner  side  of  each  hy- 
drotheca. 

Gonosome. — Gonangia  borne  profusely  on  both  faces  of  the  stem 
and  often  on  the  proximal  ends  of  the  branches ;  oblong-ovate,  with  a 
short,  small  neck  and  round  terminal  aperture,  the  gonangia  are  orna- 
mented with  about  five  compressed  longitudinal  ridges,  the  crests  of 
which  are  colored  black.     General  color  of  the  gonangia  orange  brown. 

Distribution. — Yakutat,  Alaska.     Abundant  (Harriman  Exped.). 

This  species  resembles  Sertularia  inconstans  Clark,  but  differs 
considerably,  particularly  in  its  gonosome,  which  is  very  strongly 
marked. 


2o6  NUTTING  [l88] 

Family  PLUMULARID^^. 

Trophosome. — Hydrothecag  cup-shaped,  usually  more  or  less  adnate 
to  the  stem  or  branches,  and  always  arranged  on  one  side  only  of  the 
hydrocladia,  or  branches,  on  which  they  grow.    Nematophores  present. 

Gonosome. — Reproduction  by  means  of  planulae.     No  medusae. 

PLUMULARIA. 

Trophosome. — Hydrocladia  unbranched  alternate,  nematophores  on 
slender  pedicels ;  hydrothecae  without  marginal  teeth.  Stem  not  canal- 
iculated. 

Gonosome. — Gonangia  oval,  without  corbulae  or  protective  struc- 
tures of  any  kind. 

PLUMULARIA  LAGENIFERA  Allman. 

Plumularia  lagenifera  AiAMXN,  Jour.  Linn.  See.  Zool.,  xix,  p.  157,  1885. — 
Nutting,  American  Hydroida,  Part  i,  The  Plumularidse,  p.  65,  1900. 

Plumularia  californica  Marktanner  Turneretscher,  Annalen  des  k.  k. 
Naturhist.  Hofmuseums,  v,  No.  2,  p.  255,  1890. — Nutting,  Hydroida 
from  Alaska  and  Puget  Sound,  Proc.  U.  S.  Nat.  Mus.,  Vol.  xxi,  p.  741, 
1899. 

Distribution. — Berg  Inlet,Popof  Island,  Alaska  (Harriman  Exped. )  ; 

Puget  Sound  (Nutting)  ;  Coast  of  California  (Nutting). 

PLUMULARIA   PALMERI  Nutting. 

Plumularia  palmeri  Nutting,  American  Hydroida,  Part  i,  The  Plumularidae, 
p.  65,  1900. 

Distribution. — Victoria,  B.  C.  (Harriman  Exped.)  ;  San  Diego. 
California  (Nutting) . 

This  is  the  only  species  in  the  collection  that  was  not  from  Alaska. 
It  seemed  best  to  include  it  in  the  list,  particularly  as  a  new  locality  is 
thereby  noted. 


[189]  THE    HYDROIDS  207 

BIBLIOGRAPHY. 

The  following  list  includes  all  the  publications  referred  to  in  this  Report  on 
Hydroida.     It  does  not  include  papers  that  were  consulted  and  found  to  contain 
nothing  pertinent  to  the  immediate  subject  of  the  report. 
Agassiz,  Alexander. 

1865.  North  American  Acalephae.  Illustrated  Catalogue,  Museum  Compara- 
tive Zoology,  No.  II. 

Agassiz,  Louis. 

1862.     Contributions  to  the  Natural  History  of  the  United  States,  IV. 

Alder,  Joshua. 

1857.  A  Catalogue  of  the  Zoophytes  of  Northumberland  and  Durham.  Trans. 
Tyneside  Naturalists'  Field  Club. 

Allman,  6.  J. 

1859.     Notes  on  the  Hydroid  Zoophytes.    Annals  and  Mag.  Nat.  Hist.,  Third 

Series,  Vol.  IV,  pp.  52  and  141. 
1864.     On  the  Constuction  and  Limitation  of  Genera  among  the  Hydroida. 

Annals  and  Mag.  Nat.  Hist.,  Third  Series,  Vol.  XIII,  No.  77. 
1870-1872.     Monograph  of   the  Gymnoblastic  or  Tubularian  Hydroids,  Ray 

Society. 
1888.    Report  on  the  Hydroids  dredged  by  H.  M.  S.  Challenger,  Part  2. 
1885.     Description  of  Australian,  Cape  and  other  Hydroids,  mostly  new,  from 

the  collection  of  Miss  H.  Gatty.     Journ.  Linnsean  Society,  Vol.  XIX. 

Bergh,  R.  S. 

X887.     Goplepolyper  (Hydroider)  fra  Kara-Havet. 

Bonnevie,  Kristine. 

1898      Zur  Systematik  der  Hydroiden.    Zeitschr.  Wissen.  Zoologie,  Jahrb.  63. 
1899.     Hydroida  of  the  Norwegian  North  Atlantic  Expedition. 

Calkins,  6.  M. 
1899.    Some  Hydroids  from  Puget  Sound.    Proc.  Boston  Soc.  Nat.  Hist.,  Vol. 
XXVIII,  No.  13. 

Clark,  S.  F. 

1876.  Report  on  the  Hydroids  collected  on  the  Coast  of  Alaska  and  the  Aleu- 
tian Islands,  by  W,  H.  Dall.     Proc.  Acad.  Nat.  Sciences,  Philadelphia. 

1876.  Description  of  New  and  Rare  Species  of  Hydroids  from  the  New  Eng- 
land Coast.     Trans.  Conn.  Acad.  Sci.,  III. 

1876.  The  Hydroids  of  the  Pacific  Coast  of  the  United  States,  South  of  Van- 
couver Island.    Trans.  Conn.  Acad.  Sci.,  III. 

Ellis  and  Solander. 

1786.    The  Natural  History  of  many  Curious  and  Uncommon  Zoophytes. 

Fleming,  J. 

1828.     A  History  of  British  Animals.     Edinburgh  Philos.  Journ.,  XIII. 

Hartlaub,  Clemens. 

Die  Hydromedusen  Helgolands.  Wissench.  Meeresuntersuchungen.  II 
Band. 


2o8  NUTTING  [^9°] 

Hincks,  Rev.  Thomas. 

1868    British  Hydroid  Zoophytes 

1880     On  New  Hydroida  and  Polyzoa  from  Berent's  Sea.      Annals  and  Mag. 
Nat.  Hist,,  Fifth  Series,  VI. 
Kirchenpauer,  6.  H. 

1884.    Nordische  Gattungen  und  Arten  von  Sertulariden.    Abhand.  a.  d.  Geb. 
d.  Naturwiss.,  herausgegeb.  vom  Naturwiss.,  Verein,  VIII,  Pt,  3. 
Lamarck,  J.  B.  P.  A.  de. 

1836.     Histoire  Naturelle  des  Animaux  sans  Vertebres,  2d  Edition. 
Lendenfeld,  R.  von. 

1883     Cber  Coelenteraten  der  Sudsee,  V.  Mittheilung.    Zeitschrift  fur  Wis- 
sensch.  Zoologie,  XXXVIII. 
Levinsen,  6.  M.  R. 

1886    Annulata,  Hydroida,  Anthozoa,  Porifera,  in  :  Vid.  Udbytte  af  Kanon- 
baaden,  Haucks  Togter  i. 

1892  Om  Fornyelsen  af  Ernaeringsindividerne  hos  Hydroiderne.     Ssertryk  af 
Vidensk.  Meddel.  fra  den  naturhist.     Fornening  i  Kbhvn. 

1893  Meduser,  Ctenophorer,  og  Hydroider  fra  Gronlands  Vestkyst,  Copen- 
hagen. 

Linnaeus,  C. 

1758     Systema  Naturae,  loth  Edition. 

1767     Systema  Naturae,  12th  Edition,  Pt.  II. 
Marktanner-Turaeretscher,  Gottlieb. 

1890     Die  Hydroiden  des  k.  k.  Naturhist.     Hofmuseums,  V. 

1895     Hydroiden  von  Ost-Spitzbergen.     Zool.  Jahrb.,  VIII.  Abth. 
Mereschkowsky,  C. 

1878     New  Hydroida  from  Ochotsk,  Kamtschatka,  and   other   parts   of  the 
North  Pacific  Ocean.    Annals  and  Mag.  Nat.  Hist.,  Dec. 
Nutting,  C.  C. 

1899  Hydroida  from  Alaska  and  Puget  Sound.     Proc.  U.  S.  Nat.  Museum, 
Vol.  XXI,  No.  1 171. 

1900  American  Hydroids,  Part  I.,  The  Plumularidae.     U.  S.  Nat.  Museum, 
Special  Bulletin  No.  4. 

Sars,  M.  (?) 

1862     Bemaerkninger  over  fire  norske  Hydroider;  Vid.  Selsk.  Forh. 

1873    Bidrag  til  Kundskaben  om  norges  Hydroider. 
Schultz,  Franz  Eilhard. 

1872  Nordsee  Expedition,  III,  Ccelenteraten. 
Schneider,  K.  C. 

1897     Hydropolypen  von  Rovigno,  nebst  iibersicht  iiber  das  system  der  Hy- 
dropolypen  in  allgemeinen.     Zool.  Jahrb.,  Syst.  abth.  bd.,  10. 
Segerstedt,  M. 

1899     Bidrag  til  Kannedomen   om    Hydroid-Faunen  ved  Sveriges  Vestkust, 
Stockholm. 
Verrill,  A.  £. 

1873  Brief  Contributions  to  Zoology  from  the  Museum  of  Yale  College,  No. 
XXIII,  American  Journal  of  Science. 


[ipl]  THE    HYDROIDS  2O9 

Venill,  A.  E. 

1874    Invertebrate  Animals  of  Vineyard  Sound. 

1879     Preliminary  Check  List  of   the  Marine  Invertebrates  of   the  Atlantic 
Coast,  from  Cape  Cod  to  the  Sulf  of  St.  Lawrence. 
Winther,  Georg. 

1879     Fortegnelse  over  de  i  Danmark  og  dets  Nordlige  Bilande  fundne  Hy- 
droide  Zoophyter. 
Wright,  J.  StrethiU. 

1859     Observations  on  British  Zoophytes.    Edinburgh  New  Philos.  Journ., 
New  series,  Vol.  VII. 


BR 
or  the' 

VNfVERsiTY 


"SlL/^ORMAL 


PLATE  III. 

[Proc.  Wash.  Acad.  Sci.,  Vol.  Ill,  PI.  XIV.] 

Fig.  I.   Coryne  brachiata  Nutting.     Part  of  colony. 

2.  Single  gonophore  (enlarged). 

3.  Syncoryne  eximia  Allman.     Part  of  colony. 

4.  Single  hydranth  with  budding  medusa. 

[192]  (210) 


IpR.   wash.  a.   S..   Ill,  PL.    xiv] 


H.   A.    E.   VOL.    XIII,   PLATE   III 


ALASKA    HYDROIDS 


■  or  THE 

UNIVERSITY 


PLATE  IV. 

[Proc.  Wash.  Acad.  Sci.,  Vol.  Ill,  PI.  XV.] 

Fig.  I.  Garveia  annulata  Nutting.     Part  of  colony,  showing  hydranths  and 
gonophores. 

2.  Single  hydranth,  showing  pseudo-hydrotheca  (enlarged). 

3.  Eiidendriutn  vaginatum  Allman.     Part  of  colony,  showing  hydranths 
and  gonophores. 

4.  Single  hydranth,  showing  pseudo-hydrotheca  (enlarged). 

5.  Cluster  of  female  gonophores. 

6.  Single  gonophore,  with  expanded  chitinous  collar  (enlarged). 
[19+]  (212) 


[PR.    WASH.   A.   S  ,    III,   PL.    Xv] 


H.   A.    E.   VOL.    XIM,   PLATE   IV 


ALASKA    HYDROIDS 


BRAR 
OF  THE 

UNIVERSITY 

^■LIF0R2ii> 


PLATE  V. 

[Proc.  Wash.  Acad.  Sci.,  Vol.  Ill,  PI.  XVI.] 

Fig.  I.   Tubulan'a  ^arrt'mani  Nutting.     Single  hydranth  with  gonophores. 

2.  Three  gonophores,  showing  apical  tentacles   and  developing  actinule 

(enlarged). 
[196]  (214) 


(PR.    WASH.   A.   S  ,   III,   PL.   XVlJ 


H.    A.    E.   VOL.    XIII,    PLATE  V 


ALASKA    HYDROIDS 


■  or  THE 

UNIVERSITY 
or       . 


PLATE  VI. 

[Proc.  Wash.  Acad.  Sci.,  Vol.  Ill,  PI.  XVII.] 

Tig.  I.   Clytia  calicnlata  (Hincks).     Single  hydrotheca  (enlarged). 

2.  Another  hjdrotheca  (enlarged). 

3.  Clytia  compressa  (Clark).     Hydrothecse  (enlarged)  showing  different 
degrees  of  thickening  of  the  hjdrothecal  walls. 

4.  Single  gonangium  (enlarged). 

5.  Campanularia  ritteril^vXWvi^^.     Part  of  colony  (enlarged). 
[198]  (216) 


(PR.    WASH.   A.    S  ,   111.   PL     XVIl) 


H.    A.    E.   VOL.    Xlll,    PLATE   VI 


ALASKA    HYDROIDS 


^  or  TMt 

UNIVERSITY 


PLATE  VII. 

[Proc.  Wash.  Acad.  Sci.,  Vol.  Ill,  PL  XVIII.] 

Fig.  I.  Camfanularia  reduflicata  Nutting.     Part  of  colony,  showing  hjdro- 
thecae  and  gonangium  (enlarged). 

2.  Campanularia  urceolata  Clark.     Part  of  colony,  showing  hydrothecae 
and  gonangia  (enlarged). 

3.  Camfanularia  speciosa  Clark.     Single  hydrotheca  (enlarged). 
[200]  (2l8) 


(PR.    WASH.   A.   S  ,   Ml.   PL.   XVnil 


H.    A.    E.   VOL.    Xlll,    PLATE  VII 


ALASKA    HYDROIDS 


PLATE  VIII. 

[Proc.  Wash.  Acad.  Sci.,  Vol.  Ill,  PI.  XIX.] 

Fig.  I.   Campanularia  regia  Nutting.     Single  hydrotheca,  showing  hydranth 
(much  less  enlarged  than  the  other  figures). 

2.  Another  hydrotheca,  showing  reduplication  of  margin. 

3.  Hydrotheca  of  C.  speciosa  Clark  (drawn  to  the  same  scale  as  fig.  i,  to 
show  comparative  size). 

4.  Obelia   borealis  Nutting.     Part   of    colony,   showing  hydrotheca  and 
gonangium  (enlarged). 

5  and  6.     Gonangia  (greatly  enlarged). 
[202]  (aao) 


[PR.    WASH.   A.   S.,   Ill,   PL.    Xixl 


H.   A.    E.   VOL.    XIII.   PLATE   VIII 


ELI2ABETH    B.    DtllROW,  DEL. 
AFTER    C.    C.     N. 


ALASKA    HYDROIDS 


PLATE  IX. 

[Proc.  Wash.  Acad.  Sci.,  Vol.  Ill,  PI.  XX.] 

Fig.  I.   Obelia  dudia 'Suiting.     Part  of  colony  (enlarged). 

2.   Gonotkyrcea  inornata  Nutting.     Part  of  colony,  showing  hydrothecae 

and  gonangium  (enlarged). 
3  and  4.  Gonangia  (enlarged). 
[204]  (222) 


[PR.   WASH.   A.   S  ,   in.   PL.    Xxl 


H.    A.    E.   VOL.    XIII,   PLATE   IX 


a  &CO  BAIXIHOBH. 


ALASKA    HYDROIDS 


or  THt 

VHIVERSITY 


PLATE  X. 
[Proc.  Wash.  Acad.  Sci.,  Vol.  Ill,  PI.  XXI.] 

Fig.  I.  Campanulma  rugosa'Hiutting.    Part  of  colony,  showing  hydrotheca  and 
gonangia  (enlarged). 

2.  Gonangium,  showing  developing  medusa  (enlarged). 

3.  Lafcea  adhcerens  Nutting.     Part  of  trophosome  (enlarged). 

4.  Part  of  transverse  section  of  gonosome  (enlarged). 

5.  Grammaria  immersa  Nutting.     Part  of  main  stem  (enlarged). 

6.  Portion  of  branch  with  the  peripheral  tubes  removed  to  show  connection 
of  hjdrothecae  with  axial  tube  (more  enlarged  than  fig.  5). 

[206]  (224) 


IpR.    wash.   a.   S.,   Ill,   PL.    XXl] 


H.   A.    E.   VOL.    XIII,   PLATE   X 


I  BA1.TIKORI: 


ALASKA    HYDROIDS 


PLATE  XI. 

[Proc.  Wash.  Acad.  Sci.,  Vol.  Ill,  PI.  XXII.] 

Fig.  I.  Halecium  speciosum  Nutting.     Part  of  colony,  showing  hydrophores 
and  gonangia  (enlarged). 

2.  Single  hjdranth  (greatly  enlarged). 

3.  Halecium   ornatum  Nutting.     Part  of  colony,  showing    hydrophores 
(enlarged). 

4.  Single  immature  gonangium  (enlarged). 

[208]  (236) 


[PR.    WASH.    A.   S  ,   111,   PL.   XXIl] 


H.    A.    E.   VOL.    XIII,   PLATE   XI 


ALASKA    HYDROIDS 


PLATE   XII. 

[Proc.  Wash.  Acad.  Sci.,  Vol.  Ill,  PI.  XXIII.] 

Fig.  I.  Haleciutn  reversum  Nutting.     Part  of  colony,  showing  internodes  and 
hjdrophores  (enlarged). 

2.  Single  hjdranth  with  hjdrophore  (enlarged). 

3.  Haleciutn   robustum  Nutting.     Tip  of  branch,  showing   expanded  hy- 
dranths  (enlarged). 

4.  Part  of  branch  with  soft  parts  removed  to  show  the  hydrophores  (en- 
larged). 

5.  Single  hydranth  with  its  hydrophore  (greatly  enlarged). 

[210]  (228) 


[PR.    WASH.    A.    S  ,   III.   PL,   XXIIll 


H.    A.    E.   VOL.    Xlll.   PLATE   XII 


ALASKA    HYDROIDS 


PLATE   XIII. 

[Proc.  Wash.  Acad.  Sci.,  Vol.  Ill,  PI.  XXIV.] 

Fig.   I.  Sertularella  saccata  Nutting.     Part  of  colony,  showing  hydrothecae  and 
gonangia  with  acrocysts  (enlarged). 

2.  Three  hydrothecae  (still  more  enlarged). 

3.  Single  hydrotheca,  showing  operculum  (drawn  to  same  scale  as  fig.  2). 

4.  Thuiaria  fabricii  (Levinsen).     Part  of  branch  showing  hydrothecae  and 
gonangia  (enlarged). 

5.  Front  view  of  part  of  branch  (enlarged). 

[212]  (230) 


|PR.    WASH.   A.   S  ,   111.   PL.   XXIvi 


H.   A.    E.   VOL.    Xlll,    PLATE   XIII 


ALASKA    HYDROIDS 


PLATE  XIV. 

[Proc.  Wash.  Acad.  Sci.,  Vol.  Ill,  PI.  XXV.] 

Fig.  I.   TAuiarta  eleg-ans  "Nutting. 

2.  Front  view  of  branch  (much  enlarged). 

3.  Gonangium  (much  enlarged). 

4.  Thuiaria  turgida  Clark. 

5.  Two  pairs  of  hjdrothecse  (much  enlarged). 

6.  Front  view  of  branch  (enlarged). 

[214]  (332) 


[PR.   WASH.   A.   S  .   III.   PL.   XXV) 


H.    A.    E.   VOL.    XIII,   PLATE   XIV 


OEM  a  CO   aALTIM 


ALASKA    HYDROIDS 


PLATE   XV. 

[Proc.  Wash.  Acad.  Sci.,  Vol.  Ill,  PI.  XXVI.] 

Fig.  I.   Thuiaria  coei  Nutting.     Part   of    branch,   showing    hjdrothecae   and 
gonangia  (enlarged). 

2.  Lateral  view  of  hydrotheca  (enlarged). 

3.  Single  gonangium  (enlarged). 

4.  Thuiaria    costata  Nutting.      Part  of   main  stem,  showing   origin  of 
branches  (enlarged). 

5.  Front  view  of  terminal  branches  (enlarged). 

6.  Two  pairs  of  hydrothecae  (greatly  enlarged). 

7.  8,  9.  Gonangia  (enlarged). 

[316]  (234) 


[pR.    WASH.   A.   S  ,   III,   PL.   XXVll 


H.   A.    E.   VOL.   XIM,    PLATE   XV 


ALASKA    HYDROIDS 


raTt 

^'or  THt 
INIVER8ITY 


INDEX 


New  genera  and  species  and  the  pages  on  which  they  are  described  are  in 
black-face  type ;  synonyms  in  parenthesis  ;  pages  where  synonymy  of  known 
species  or  genera  is  given  in  italics;  subspecies  are  treated  as  species  for  the 
purposes  of  the  Index. 


Acanthinula  21 

aculeata  21 

harpa  (22) 
Acella  (60),  64,  72 

kirtlandiana  ^2 
Achatinidae  33 
Acmsea  113 
Acroloxus  108,  109 
Acroxus  (108) 
Adelina  (60) 

elegans  60 
Adula  (82) 
Agriolimax  ^5 

agrestis  ^5 

berendti  ^6 

campestris  46 

hyperboreus  ^j" 
Alasmidonta  costata  (131) 
Alasmodon  falcata  (132) 

rhombica  (127) 

yubaensis  (132) 
Alasmodonta  arcuata  (132) 

complanata  (131) 

dahurica  (132) 

rugosa  (131) 
Amalia  46 

gagates  46 

hewstoni  46 
Ameria  loi 
Amnicola  7/7 

cincinnatiensis  118 

emarginata  118 

granum  (118) 

hindsii  (119) 

lapidaria  (119) 

limosa  7/7 

pallida  777 


Amnicola  porata  (117) 
Amnicolidae  777 
Amphibina^j 

avara  55 

pfeifferi  55 
Amphibulima  (55) 

cuculata  55 

patula  55 
Amphibulimus  (55) 
Amphibulina  (55) 
Amphipeplea  78 
Amplexa  (104) 
Amplexis  (22) 
Amplexus  (22),  (104) 
Ancaeus  (82) 
Ancylastrum  108,  109 

cumingianus  108 
Ancyllus  (108) 
Ancylus  11,  707,  (108),  109 

caurinus  (iio) 

cumingianus  108,  109 

fluviatilis  107,  108,  109 

fragilis  iio 

fuscus  109 

kootaniensis  770 

lacustris  107,  108,  109 

newberryi  109 

parallelus  no 

patelloides  109 

radiatus  108 

rivularis  709,  (no) 
Anguispira  alternata  (49) 

bruneri  (52) 
Angustula  milium  (32) 
Anisopsis  (81),  85 
Anisus  81,  (82;,  84 
Anodon  areolatus  (127) 


(235) 


236 


INDEX 


Anodon  biangulata  (130) 
exilis  (129) 
feminalis  (130) 
rostratus  (128) 
rugosus  (127) 
triangularis  (128) 

Anodonta  J3y 

angulata  (130) 
argentea  (131) 
arkansasensis  (127) 
beringiana  10,  I2J 
biangulata  (130) 
buchanensis  (131) 
cellensis  (127) 
cognata  (128) 
dallasiana  (130) 
denigrata  (131) 
edentula  (127) 
feminalis  (130) 
ferruginea  (131) 
ferussaciana  (130) 
flava  (i29)_ 
footiana  (129),  129 
fragilis  (129) 
gigantea  (129) 
glandulosa  (129) 
grandis  I2g 
housatonica  (129) 
impHcata  i2g 
irisans  (129) 
kennerleyi  128 
kennicotti  130 
lacustris  (129) 
laosensis  (128) 
lewisii  (129) 
marginata  128 
marrjattiana  (129) 
modesta  (131) 
newtonensis  (129) 
nuttalliana  128 
oblita  (131) 
oregonensis  128 
ovata  (129) 
pallida  (129) 
pavonia  (127) 
pepiniana  130 
plicata  (131) 
randalli  (130) 
rotundata  (128) 


Anodonta  rotundovata  (128) 

salmonea  (127),  (129) 

shaefferiana  (127) 

showalteri  (127) 

simpsoniana  (130) 

subcarinata  (129) 

subcylindracea  (131) 

tetragon  a  (127) 

triangularis  (128) 

undulata  (127) 

wahlamatensis  128 

•wardiana  (127) 

youconensis  (127) 

youkanensis  (127) 
Anodontoides  130 

ferussacianus  130 
Ansulus  (108) 
Ansylus  (108) 
Aplecta  (104),  106 
Aplexa  100,  102,  70^,  105,  107 

hordacea  103 

hypnorum  12,  104,  105,  /0<J,  I07 
Aplexus  (104) 

hypnorum  107 
Arctonchis  112 

borealis  112 
Arianta  arbustorum  21 
Ariolimax  34,  35,  47 

columbianus  4Jy  48 

maculatus  48 

steindachneri  ^5 

stramineus  48 
Arion  andersoni  (46) 

foliolatus  (47) 
Arionidae  46 

Arionta  ptychophora  (25) 
Armiger  <Sj,  86 

crista  96 
Arnouldia  (40) 

fulva  (41) 
Aulaca  (21) 
Auricella  (115) 
Auricula  (115) 
Auricularia  (60) 
Auriculidse  115 
Auriculina  (115) 

Bathyomphalus  83,  86 
Bifidaria  27 


INDEX 


237 


Bifidaria  armifera  2j 

contracta  27 

holzingeri  28 

pentodon  28 
Bornia  141 

Brachyspira  (55)  __, 

Brondelia  109  "^ '"'^ 

drouetiana  109 
Buccinum  palustre  62,  (76) 

truncatulum  62,  (72) 
Buliminus  obscurus  41 
Bulimnea  (60),  63 

megasoma  67,  70 
Bulimulus  pilula  79 
Bulimus  (104),  105,  (115) 

harpa  (21) 

hjpnorum  (106) 

lubricoides  (33) 
BuHnus  (100),  (loi),  (1C4),  105,  107 

hordaceus  (104) 

hjpnorum  107 

per  la  105 

pictus  107 

senegalensis  105 

turritus  105 
Bulla  (104) 

fontinalis  99,  loO 

hypnorum  104,  105,  (106) 

turrita  (106) 
BuUinus  (100),  (104) 

fontinalis  icx) 

turritus  (106) 
Bythinella  obtusa  118 
Bythinia  105 

Caillaudia  (81) 

angulata  81 
Calycella  194 

syringa  177,  194-^95 
Campanularia  189 

caliculata  ( 188) 

compressa  (188) 

crenata  (190) 

denticulata  177,  189 

gracillima  (195) 

grandis  191 

lineata  177,  189 

reduplicata  177,  190,  218 

regia  177,  xgo,  220 


Campanularia  ritteri  177,  z8g,  216 

serpens  (197) 

speciosa  177,  189-190,  218,  220 

urceolata  177,  190,  218 

verticillata  177,  189 
CampanuHna  194 

rugosa  177,  194,  224 
Campeloma  124 

decisum  124,  125 
Carinifex  63 
Carychium  //j,  1 16 

exiguum  115,  n6 

exile  1/6 

minimum  115 
Cepaea  hortensis  (20) 
Chilostoma  (22) 
Chlamydea  36 
Choanomphalus  62 
Cincinna  (120) 

Cincinnatia  cincinnatiensis  118 
Cionella  lubrica  (33) 
Circinaria  (22),  33 

chocolata  34 

hemphilli  35 

hybrida  jj 

sportella  34,  33 

vancouverensis  25,  34,  (35) 

voyana  35 
Circinariidae  33 
Clytia  188 

caliculata  177,  188,  216 

compressa  177,  188,  216 

Integra  188 
Cobresia  (35),  121 
Cochlicopa  33 

lubrica  33 
Cochlohydra  (55) 
Complanaria  gigas  (131) 
Concinna  (120) 
Conulus  (39) 

alaskensis  41 

arcticus  (45) 

chersinus  (41) 

fulvus  (40),  (41) 

trochiformis  (41) 
Coppinia  arcta  175 
Coretus  (80),  (81),  83 
Corneocyclas  3,  134,  141 

abdita  142,  143,  145 


238 


INDEX 


Corneocyclas  abyssorum  143 

aequilateralis  141 

arctica  144 

borealis  144 

compressa  142 

glacialis  144 

henslowana  14S 

idahoensis  141 

nivalis  144 

occidentalis  143 

pulchella  144 

randolphi  144 

rotundata  143 

scutellata  141 

sibirica  144 

steenbuchii  143 

ultramontana  144 

variabilis  142 

ventricosa  143 

virginica  141 
Cornu  (81) 
Coryne  183 

brachiata  177,  183,  210 

eximia  (184) 
Costatella  (100),  jox 
Costella  (100) 
Cotulina  polyzonias  (201) 

tricuspidata  (201) 
Cumingia  (108) 
Cyclas  appendiculata  (145) 

aurea  (135) 

bulbosa  136 

calyculata  140 

dentata  (137) 

dubia  (141) 

elegans  (136) 

cmarginata  (138) 

fabalis  (137) 

flava  (138) 

fuscata  136 

jayensis  (139) 

lenticula  140 

media  (140) 

nobilis  (137) 

ovalis  (137) 

partumeia  (139) 

patella  (138) 

pulchella  (144) 

rhomboida  (136) 


Cyclas  saratogea  (135) 

similis  (134) 

solidula  (136) 

stagnicola  (140) 

staminea  (136) 

steenbuchii  (143) 

striatina  (135) 

sulcata  (134) 

tenuis  139 

transversa  (139) 

truncata  (140) 
Cyclocalyx  143 
Cyclolimnaea  64 
Cyclostoma  lapidaria  (119) 

tricarinata  (121) 
Cymatocyclas  compressa  142 

Dall,  W.    H.,  land    and    fresh  water 

mollusks  1-171 
Dentati  97 
Dentatus  (97) 
Diastropha  (99) 
contorta  100 
Diplodiscus  (82),  85,  86 
Discoidina  (83) 
Discus  (97) 
Drepanotrema  82,  86 

Endodontidse  49 
Enydra  (99) 
Epiphragmophora  21 

fidelis  21 
Erinna  (61),  62,  65 

newcombi  61,  65 
Euconulus  J9,  40,  45 

fabricii  41,  42 

f  ulva  42 

fulvus  39,  (40),  (41) 

trochiformis  40,  41,  42 
Eucopella  campanularia  (188) 
Eudendrium  annulatum  186 

bacciferum  (184) 

pygmaeum  186 

vaginatum  177,  182,  185,  212 
Euhadra  fiscina  II 
Eulimneus  (61) 
Eulota  fiscina  11 

flexibilis  11 

weyrichi  11 


INDEX 


239 


Ferrissia  109 

parallelus  no 

rivularis  no 
Ferussacia  subc^lindrica  (33) 
Filellum  197 

serpens  177,  797 
Fluminicola/zp  "^ 

nuttalliana  iig 

virens  iig 
Fossaria  (61) 

Galba  (60),  62,  64 

desidiosa  73 

galbana  73 

holboUi  74 

humilis  73 

truncatula  72 

vahlii  74 
Gallandia  (36) 
Garveia  i8| 

annalata  177,  184,  213 

nutans  177,  184. 
Gastrodonta  43 

gularis  43 
Giraulus  (83) 
Glaphyra  (22) 
Glyptophjsa  loi 
Gonidea  130 

angulata  130 
Goniobasis  116,  117 

pHcifera  116,  117 

silicula  1161  117 
Gonothyraea  193 

inornata  177,  193,  223 
Gonyodiscus  jo 

stxiatella  (50) 
Grammaria  196 

immersa  177,  ig6,  224 
Gulnaria  (60) 
Gundlachia  /o5,  109 

ancyliformis  108 
Gyraulus  <Sj,  86 

deflectus  94 

hirsutus  93 
Gyrorbis  (82),  85,  (120) 
Gyrulus  (83) 

Haldemania  (108) 
Haldemanina  97,  98 


Halecium  197 

halecinum  177,  igy-igS 
muricatum  177,  ig8 
ornatom  177,  199,  226 
reversum  177,  198,  228 
robastum  177,  200,  228 
scutum  177,  198 
speciosam  177,  199,  226 
Harriman,   E.  H.,  species  named  for 

186 
Hebella  193 

pocillum  177,  ig3 
Helicidae  3,  19,  20 
Helicodiscus  52 
lineatus  52 
Helicogona  subpersonata  1 1 
HelicoHmax  (35),  (36) 
Helisiga  (55) 

sanctaehelenae  55 
Helisigna  (55) 
Helisoma  81,  84,  85 
bicarinatus  87 
Helix  20,  (39),  (59),  (115) 
albolabris  (26) 
alternata  (49) 
amarula  59 
amurensis  (21) 
arborea  (42) 
arboreus  (42) 
arbustorum  (21) 
asiatica  (23) 
asteriscus  (51) 
attenuata  54 
auricularia  (60) 
baskervillei  (24) 
belcheri  54 
bidentata  41 
brewer i  (42) 
chersina  (41),  42 
Columbiana  (24) 
conspecta  (53) 
cooperi  52 
cornea  80,  81 
corneus  80 
costata  (23) 
crenella  (23) 
cronkhitei  (50) 
devia  (24) 
dubia  (49) 


240 


INDEX 


Helix  egena  (41),  42 
electrina  (38) 
engonata  (87) 
fabricii  (41) 
fidelis  (21) 
floccata  51 
fulva  (40) 
germana  (25) 
gularis  (43),  44 
hammonis  (38),  42 
harpa  (21) 
haydeni  (52) 
hortensis  20 
indentata  (39) 
labiosa  (24) 
labyrinthica  (27) 
limitaris  (49) 
Hneata  (52) 
lubrica  (33) 
lucida  (42) 
mandralisci  (40) 
milium  (43) 
minuscula  (43) 
minuta  (22) 
minutissima  (53) 
monodon  (26) 
morsei  (39) 
mortoni  (40) 
nitida  41,  (42) 
nitidula  (39),  (40) 
nuttalliana  (21) 
paludosa  (22) 
pellucida  35,  (36) 
planorbis  (80),  81 
ptychophora  (25) 
pulchella  (22),  (23) 
putris  55 
pjgmaea  (53) 
radiatula  (38) 
rudis  54 
solitaria  (49) 
spirorbis  83 
sportella  (35) 

stagnalis  59,  (60),  (62),  (65) 
striatella  (50) 
strigosa  (51) 
subglobosa  (20) 
townsendiana  (25) 
trochiformis  (40) 


Helix  trochilus  (40) 

trochulus  (40),  41 

vancouverensis  (34) 

vellicata  (34) 

virgata  52 
Hemithalamus  (97) 

nitidus  97 
Hemphillia  48 

camelus  48 

glandulosa  48 
Heterodiscus  (82),  83 
Hippeutes  (82) 
Hippeutis  82,  86,  (97) 
Hjalina  (35),  (39) 

arborea  (42) 

arctica  (45) 

binnejana  (39) 

binneyi  (39) 

fulva  (40),  (41) 

indentata  (39) 

nitida  (42) 

pellucida  (38) 

viridula  (38) 
Hyalinia  (39) 

fulva  (40) 

trochiformis  (41) 
Hydroids  173-234 

bibliography  207-209 

genera  and  species,  systematic  dis- 
cussion 181-206 

geographic  distribution  176-180 

plates  and  plate  descriptions  210- 
234 

lelskia  (120) 
Isidora  loo,  loi,  105 

wahlbergi  loi 
Isthmia  ventricosa  (31) 

pygmsea  33 

Jelskia  (120),  121 

Laevapex  109 

fragilis  110 

kootaniensis  lio 
Lafoea  175,  181,  193,  195 

adhsrens  177,  ig6,  224 

dumosa  177,  179,  igj 

fruticosa  177,  196 


INDEX 


241 


Lafoea  gracillima  177,  igj 

pocillum  (193) 
Lampsilis  12^ 

alatus  126,  127 

borealis  126 

ellipsiformis  126 

gracilis  127 

ligamentinus  126 

luteolus  12^ 

radiatus  126 

rectus  126 

superiorensis  125 

ventricosus  12^ 
Lantzia.     See  Erinna. 
Lanx  109 
Lasmigona  131 
Leach  ia  (60) 

stagnalis  60 
Legrandia  (108) 
Le  Liri  iii 

Leptolimnaea  glaber  64 
Leptolimnea  (60),  62,  64 

elongata  60 

glaber  60 
Leptolimneus  (61) 

glaber  61 
Limacidse  45 
Limacina  (35) 
Limax  agrestis  (45) 

berendti  46 

columbianus  (47) 

hemphilli  46 

hewstoni  (46) 

hjperborea  (45) 
Limnaea  (60),  (61),  62,  (105) 

ampla  (68),  (69) 

angulata  (68) 

arctica  (75) 

binneyi  (69) 

bulimoides  (79) 

canadensis  (69) 

decisa  (125) 

decollata  (68) 

elodes  (76) 

elongata  (75) 

emarginata  (69) 

exilis  (72),  77 

ferruginea  (72) 

glabra  61 


imnaea  gronlandica  (75) 

hajdeni  (76) 

holbolli  (74) 

king!  61 

kirtlandiana  (72) 

lanceata  (72) 

leucostoma  (75) 

megalosoma  (67) 

megastoma  (67) 

mighelsi  (68) 

minor  (75) 

molleri  (75) 

nuttalHana  (76) 

philadelphica  (74) 

plebeia  (76) 

proxima  (76) 

scalaris  (69) 

senegalensis  (75) 

6tagnalis  (65) 

traski  (74) 

umbilicata  (79) 

vahlii  (74) 

velutina  61,  65 
Limnaeus  decollatus  (68) 

elodes  (76) 

elongatus  (77) 
Limnea  (60) 

adelinae  (78) 

caperata  (79) 

catascopium  (68) 

cochlea  (59) 

columella  (70) 

desidiosa  (73) 

expansa  (76) 

fragilis  (76) 

galbana  (74) 

gracilis  60 

humilis  (73) 

megasoma  60,  (67) 

serrata  (69) 
Limneus  (60) 

desidiosus  (73) 

emarginatus  (68) 

minutus  (72) 

ontariensis  (68) 

palustris  (76) 

stagnalis  (60) 

umbrosus  (77) 
Limnophjsa  (60),  62 


242 


INDEX 


Limnophysa  holboUi  (74) 

palustris  60 

senegalensis  75 

vahlii  (74) 
Limnus  (61) 
Liria  (iii) 
Liriola  /// 

thersites  III 
Lucena  (22),  55 

oblonga  55 

pulchella  55 
Lucina  lenticula  140 
Lymnaea  jp,  60,  61,  62,  63,  66,  68,  72, 
100,  102 

acuta  80 

adelinae  yS 

ampla  71,  72 

anticostiana  79 

appressa  (65) 

arenaria  63 

atkaensis  66 

auricularia  60, 61,  62,  64 

binneji  6p,  70 

bulimoides  78,  jg 

canadensis  68 

caperata  yg 

catascopium  77,  78,  79 

columella  70 

desidiosa  7J,  75,  80 

emarginata  68, 69 

expansa  77 

ferruginea  73 

fossaria  80 

galbana  73 

glaber  60,  62 

glabra  60 

gracilis  64 

haydeni  77 

holbolli  74 

humilis  7J 

involuta  64 

jugularis  (65) 

kingi  64 

kirtlandiana  72 

lagorii  61,  63 

lanceata  72 

lepida  67 

malleata  75 

megasoma  63,  67,  70 


Lymnsea  mighelsi  68,  72 

nitida  75 

nuttalliana  77 

obrussa  73 

opacina  80 

palustris  62,  64,  68,  75,  76,  78 

pereger  60 

perpolita  78 

petersi  66 

petitii  80 

pingelii  (75) 

preblei  70 

proxima  74,  77 

randolphi  66,  7/ 

reflexa  60,  62,  72,  77 

rowelli  76 

solida  78 

solidula  75 

stagnalis  61,  63,  6^,  66 

sumassi  66,  69,  71,  72,  (77),  78 

techella  78,  79 

tenuicostata  64 

traskii  74 

truncatula  60,  61,  62,  64,  72,  73 

trjoni  74 

trjoniana  74 

vahlii  74.,  75 

wormskioldi  (75) 

zrmanjse  61,  65 
L.ymnaeidae5p 
Lymnaeus  (60) 

columellus  (70) 

emarginatus  (68) 
Ljmnea  (60) 

cornea  (77) 
Ljmneus  (60) 

caperatus  (79) 

desidiosus  (73) 

emarginatus  (68) 

galbanus  (73) 

humilis  (73) 

megasomus  (67) 

minutus  (72) 

reflexus  (77) 
Lymnophysa  (61) 
Lymnula  (60) 
Lymnus  (60) 
Lyogyrus  118 

granum  I18,  II9 


INDBX 


243 


Lyogjrus  lehnerti  (117) 

MacrocjcHs  33 

vancouverensis  (34) 
Macrophysa  (100),  loi 
Margarita  oregonensis  ( 128) 
Margaritana  131  ^_^  — =- 

falcata  132 

margaritifera  11,  132 
Melania  117 

canaliculata  (116) 

conica  (116) 

plicifera  (116) 

silicula  (116) 
Melantho  decisa  (125) 
Menetus  (81),  5^,86 

exacuous  91 

opercularis  92 
Merriam,  C.  Hart,  preface  v 
Microphysa  99 

lansingi  44 

pygmsea  (53) 

stearnsii  (44) 
Mollusks  1-17 1 

bibliography  147-153 

fresh  water  shells,  distribution  1-6. 

9-15 

genera  and  species,  systematic  dis- 
cussion 19-145 

land  shells,  distribution  7-15 

plates  and  plate  descriptions  154, 
156 
Mouretia  (iii) 
Muretia  (iii) 
Musculium  jayanum  139 

lenticula  140 

partumeium  139 

raymondi  138 

tenue  139 

transversum  139 

truncatum  140 
My  a  complanata  (133) 

margaritifera  (132) 

radiata  (126) 
Myxas  (104) 

Naiades  12^ 
Nauta  (104) 

hypnorum  (106),  (107) 


Nauta  polaris  (107) 
Nautilina  (83) 
Nautilus  crista  (96) 

lacustris  97 
Neritostoma  jj,  (61) 
Nutting,  C.  C,  hydroids  173-234 

Obelia  191 

borealis  177,  192,  220 

dichotoma  177,  igi 

dubia  177,  192,  222 

plicata  177,  191 
Odostomia  (115) 
Oligolimax  (36) 
Omphalia  (61) 
Omphalolimnus  (61),  63 
Omphiscola  60,  (61),  62 
Onchidella  iiz 

borealis  112,  113,  114 

carpenteri  113 

celtica  112,  113,  114 

floridana  114 
Onchidiidse  112 
Onchidium  II2,  114,  115 

boreale  (112) 

celticum  113 

nigricans  112 

Schramm!  114 

typhae  112 
Orbis  (81) 
Oreohelix  5/ 

cooperi  52 

stantoni  52 

strigosa  5/,  52 
Oxyloma  55 

hungarica  55 

Pagana  (36) 

Paludina  cincinnatiensis  I18 

decisa  (125) 

emarginata  (118) 

grana  (118) 

hyalina  (91) 

limosa  (117) 

lustrica  120 

nuclea  (119) 

obtusa  ( 1 18) 

porata  (117) 

seminalis  (119) 


244 


INDEX 


Palundina  virens  ( 1 19) 
Paraspira  8a,  86 
Parmacellina  (36) 

vitrinaeformis  36 
Parjpha  microcephala  187 
Patella  (107) 

lacustris  107,  108 
Patula  49 

asteriscus  (51) 

cronkhitei  (50) 

occidentalis  4g 

pauper  50,  51 

solitaria  (49) 

striatella  50 
Patulastra  pugetensis  (43) 
Periophthalmus  115 
Petasia  (39) 

fabricii  (41) 

fulva  40 

trochiformis  (40) 
Phenacarion  foliolatus  (47) 

hemphilli  (47) 
Phenacolimax  (36) 
Phymesoda  dubia  (141) 

idahoensis  (141) 

scutellata  141 

virginica  141 
Physa  II,  63,  (81),  84,  gg,  (100),  lOl, 
102,  (104),  105,  107 

albofilata  (102) 

ampul  lacea  103 

ancillaria  102 

bullata  (103) 

columnaris  99,  lOl 

contorta  99 

costata  100,  loi 

crassa  (102) 

elongata  (106) 

elongatina  (107) 

fontinalis  II,  99,  (102),  105 

fragilis  (loi) 

glabra  (106) 

globosa  99 

guildingii  99,  100 

gyrina  loi 

heterostropha  /o/,  103 

hildrethiana  102 

hordeacea  10 j,  107 

hjpnorum  (106) 


Physa  lata  (loi) 
lord!  102,  103 
microstoma  99 
obesa  (102) 
oleacea  (102) 
parkeri  (102),  103 
philippii  (loi) 
plicata  (101) 
polaris  107 
primeana  (loi) 
propinqua  103 
turrita  (106) 
vinosa  102 

Physastra  (61),  62,  64 
vestita  61,  64 

Physella  (99),  100 

Phjsidae  gg,  loi 

Physodon  (99),  lOO 

Physopsis  100,  lOl 

Phyza  (99),  (104) 

Pierosoma  81,  85 
binneyi  87 
corpulentus  87,  88 
trivolvis  88 

Pisidium  3,  141 

abditum  (142),  (143) 
abyssomus  (143) 
abyssorum  (143) 
sequilaterale  (141) 
arcticum  (144) 
boreale  (144) 
compressum  (142) 
glaciale  (144) 
henslowianum  (145) 
idahoense  (141) 
nivale  (144) 
occidentale  (143) 
randolphi (145) 
rotundatum  (143) 
scutellatum  (141) 
sibiricum  (144) 
steenbuchii  (143) 
ultramontanum  (144) 
variabile  (142) 
ventricosum  (143) 
virginicum  (141) 

Planaria  (83) 

Planella  (120) 

Planogyra  51 


INDEX 


24s 


Planogyra  asteriscus  5/,  122 
Planorbarius  (81) 
Planorbe  brun  80 
Planorbella  81,  85 

campanulatus  90 
Planorbina  81,  83,  84 

glabrata  86 
Planorbis   63,  80,  81,  82,  83,  84,  102, 
(104),  105 

alabamensis  92 

albus  83,  86,  (93),  94 

ammon  88 

andecolus  81 

arcticus  g6 

armatus  97 

armiger  97,  (98),  99 

armigerus  97,  (98) 

bellus  (90) 

bicarinatus  81,  84,  8^ 

bilUngsi  (95) 

binneyi  87,  88,  89 

boissyi  82 

borealis  (93),  94 

brongniartiana  91 

buchanensis  92 

calculus  81 

callioglyptus  (92),  93 

campanulatus  81,  85,  go 

carinatus  82 

centervillensis  (92),  93 

complanatus  82,  85,  90 

concavus  (95) 

contortus  83,  86 

corneus  80,  81,  83,  84 

cornu-arietis  84 

corpulentus  87 

costatus  (96) 

crista  g6 

cristatus  (96) 

decHvis  98 

deflectus  9^ 

dilatatus  92 

disjectus  89 

draparnaldi  94 

draparnaudi  94 

elevatus  (95) 

engonatus  (87) 

exacuous  9/,  92,  93 

exacutus  (91) 


Planorbis  fontanus  82,  86 

glabratus  86 

guadeloupensis  81 

hirsutus  pj,  94 

hispidus  83 

hornii  89,  90 

imbricatus  (96) 

lacustris  97 

lens  91 

lentus  (86),  (88) 

libanicus  82,  83 

limophilus  95 

lineatus  97 

lory!  81 

macrostomus  (88),  8g,  90 

major  87 

marginatus  82 

megas  gi 

multivolvis  82,  85 

nathorsti  g6 

nautileus  (96) 

nitidus  97 

obliquus  94 

occidentalis  89 

olivaceus  84 

opercularis  82,  86,  g2 

oregonensis  89,  (92),  93 

parallelus  (52) 

parvus  83,  86,  pj",  96 

planulatus  g2,  93 

rotundatus  82,  86 

rudentis  90,  91 

subcrenatus  (88),  89,  90 

traskii  88 

trivolvis  81,  85,  87,  88,  89,  90 

tumens  88,  89 

turritus  (106) 

umbilicatellus  g6 

umbilicatus  82,  85,  (96) 

vermicularis  pj 

virens  g<f 

vortex  82,  85 

vulgaris  82 

wheatleyi  97,  98 

yzabalensis  82,  86 
Planorbula  (97),  98 

armigera  98 

christyi  99 
Plesiophysa  loi 


246 


INDEX 


Pleurocera  iib 

canaliculata  Jib 
Pleurolimnaea  (60),  63,  64 

tenuicostata  60 
Plumularia  206 

californica  (206) 

lagenifera  177,  20b 

palmeri  177,  206 
Poeyia  (108) 

gundlachioides  108 
Polita  (39) 

fulva  (40) 
Polygyra  24 

albolabris  2b 

Columbiana  24,  34 

devia  24 

germana  2^y  26 

labiosa  (24) 

megasoma  26 

monodon  2b 

ptjchophora  2^ 

santacruzensis  24 

townsendiana  23 
Poljgyrus  (83) 
Polyrhjtis  (61),  63,  64 
Pomatiopsis  iig 

lapidaria  119,  (120) 
Pompholjx  63 
Primella  rajmondi  (139) 
Pristiloma  44 

arctica  4s 

idahoense  44 

lansingi  44 

pilsbrji  44 

stearnsi  (44),  45 

stearnsii  44 

taylori  44 
Prophysaon  4b 

andersoni  4b 

cceruleum  41 

dubium  (47) 

fasciatum  (47) 

fiavum  (46) 

foHolatum  47 

hemphilli  (46),  47 

humile  4f 

marmoratum  (46) 

obscurum  (47) 

pacificum  (46) 


Prophysaon  pallidum  (46) 

suffusum  (46) 
Proptera  alatus  (127) 
Protancylus  109 
Pseudohyalina  minuscula  (43) 

pugetensis  (43) 
Pterosygna  131 
Pulmobranchia  loi 
Punctum  5J 

asteriscus  53 

clappi5i,5j 

conspectum  10,  Jj 

minutissimum  (53) 

pugetensis  (43) 

pygmaeum  S3 

randolphi  §3 
Pupa  alticola  (54) 

arctica  (32) 

armifera  (27) 

badia  (28) 

bigranata  (28) 

blandi  (28) 

columella  (54) 

contracta  (27) 

corpulenta  (29) 

costulata  (21) 

decora  (29) 

edentula  (54) 

exigua  (116) 

gouldii  (30) 

gredleri  (54) 

holzingeri  (28) 

hoppii  (29) 

lundstromi  (28) 

milium  (32) 

modesta  (29) 

pentodon  (28) 

pygmaea  (33) 

signata  (28) 

simplex  (54) 

steenbuchi  (29) 

superioris  (33) 
Pupidae  27 
Pupilla  2B 

badia  (28),  (29) 

blandi  28 

muscorum  28 ,  (39) 
Pyramidula  49 

alternata  4g 


INDEX 


247 


Pyramidula  asteriscus  $* 
cronkhitei  jo,  51 
Hmitaris  4g 
randolphi  (53) 
ruderata  50,  51 
soHtaria  ^9 
striatella  j'o 

Quadrula  133 
heros  133 
hippopaea  133 
lachrymosa  134 
plicata  133 
rubiginosa  134 
undulata  133 

Radix  (60),  62,  63,  64,  65,  67,  68,  71,  72 

binneyi  69 

columella  70 

mighelsi  68 

randolphi  71 
Rivicola  (99) 

Sandria  65 
Saraphia  (115) 

tridentata  115 
Segmentaria  (97) 
Segmentina  gy,  98 

armigera  9^ 

christyi  99 
Selenites  33 

vancouverensis  (34) 
Semilimax  (35),  (36) 
Sertularella  200 

conica  (201) 

geniculata  (202) 

polyzonias  177,  20t 

rugosa  (201) 

saccata  177,  201-202,  230 

tricuspidata  177,  20J 
Sertularia  argentea  179,  (202),  204 

cupressoides  (203) 

dichotoma  (191) 

dumosa  (195) 

fabricii  (203),  204 

halecina  (197) 

muricata  ( 198) 

polyzonias  (201) 

similis  (203) 


Sertularia  syringa  ( 194) 

thuiarioides  (204) 

tricuspidata  (201) 

variabilis  (203) 

verticillata  (189) 
Siphonaria  /// 

eipho  III 

thersites  iii 
Siphonariidae  /// 
Sphaeriidae  134,  145 
Sphaerium  134 

aureum  135 

cooperianum  (139) 

corneum  135 

dentatum  136,  13^ 

emarginatum  138 

fabale  137 

fabalis  (136) 

flavum  138 

jayanum  i3g 

lenticula  140 

medium  140 

nobile  137 

occidentale  136,  /j/ 

partumeium  i3g 

patella  138 

primeanum  141 

raymondi  138 

rhomboideum  136,  141 

simile  134 

solidulum  136 

spokani 138 

stagnicola  140 

stamineum  136 

striatinum  13^ 

sulcatum  (134) 

tenue  /j^,  140 

transversum  i3g 

truncatum  140 

tumidum  138 

walker  i  135 
Sphy  radium  ^4 

edentulum  34 
Spiralina  (81) 
Spirodiscus  corneus  (81) 
Spirorbis  (82) 
Stagnicola  (60),  62,  64,  68,  71.  72,  74 

adelinae  78 

•nticostiana  79 


248 


INDEX 


Stagnicola  bulimoides  79 

caperata  79 

catascopium  77 

communis  (76) 

emarginata  68 

palustris  76 

perpolita  78 

reflexa  77 
Stenotrema  germanum  (35) 
Strepomatidae  116 
Striatura  milium  (43) 
Strobila  labjrinthica  27 
Strophitus  727 

edentulus  (127) 

rugosus  127 
Succinea  (55).  55.  7i.iOS 

alaskana  58 

annexa  (59) 

aurelia  (59) 

avara  55,  56,  57 

campestris  (58) 

chrjsis  10,  5p 

decampi  (56) 

dunkeri  55 

elegans  55 

greeri  (58) 

gronlandica  57 

grosvenori  57 

hawkinsi57 

haydeni  (56) 

lineata  (59) 

minor  (56) 

nuttalliana  jS 

obliqua  j8 

oblonga  55 

oregonensis  j<5 

ovalis55,  (56),  (58),  59 

pfeifferi  55 

putris  55 

retusa  (56),  57,  58 

rusticana  j8 

sillimani  57 

totteniana  55 

vermeta  (57) 

verrilli  57 

wardiana  (57) 
Succineidae  55 
Succinia  (55) 
Symphynota  131 


Symphynota  complanata  131 

costata  iji 

katherinse  131 
Syncoryne  183 

eximia  177,  184,  210 

Tanousia  (61),  62,  65 

Tapada  (55) 

Taphius  (81),  85 

Teba  (39) 

Tellina  henslowana  (145) 

virginica  (141) 
Thuiaria  202 

argentea  177,  202-203 

coei  177,  203,  234 

costata  177,  205,  234 

cupressoides  177,  203 

elegans  177,  205,  232 

fabricii  177,  203-204,  230 

gigantea  177,  204 

similis  177,  203 

thuiarioides  177,  204 

turgida  177,  204,  232 

variabilis  177,  203 
Torquis  83,  86 

arcticus  96 

nathorsti  96 

parvus  95 

umbilicatellus  96 

vermicularis  95 
Trimusculus  (iii) 
Trochilus  mortoni  40 
Trochlea  (83) 
Trochovitrina  (36) 
Trochula  40 
Trochulus  (40) 

trochiformis  (41) 
Trochus  (39) 

terrestris  (40) 
Trophidiscus  (82) 
Tropidina  (120),  121 
Tropidiscus  (81),  82,  85 
Tropidocyclas  henslowana  145 
Truella  (55) 

elongata  55 
Tubular  ia  186 

borealis  187 

elegans  187 

harrimani  177,  186,  214 


INDEX 


249 


Tubularia  larynx  187 
Turbo  (104),  (115) 

muscorum  (28) 

nautileus  (96) 

stagnalis  (106) 

Unio  II,  133 
alatus  (126) 
asperrimus  (134) 
borealis  (126) 
complanatus  (132),  /jj 
costatus  (133) 
crassus  (126),  (133) 
dahuricus  (132) 
ellipsiformis  (126) 
elongatus  (132) 
falcatus  (132) 
flavus  (134) 
gracilis  (127) 
heros  (133) 
hippopaeus  (133) 
katherinae  (131) 
lachrjmosus  (134) 
ligamentinus  (126) 
luteolus  (125) 
mongolicus  (132) 
multiplicatus  (133) 
pictorum  13 
plicatus  (133) 
quadrulus  (134) 
radiatus  (126) 
rectus  (126) 
rubiginosus  (134) 
sinuatus  (132) 
spatulatus  (126) 
trigonus  (134) 
undulatus  (133) 
ventricosus  (125) 

Vallonia  22 

albula  2j 

asiatica  23 

costata  23 

gracilicosta  23 

minuta  (22) 

pulchella  22,  23 

rosalia  (23) 
Valvata  85,  (120) 

carinata  (121) 


Valvata  confusa  (121) 

cristata  120,  122,  124 

helicoidea  123 

humeralis  121 

jelskii  120,  121 

lewis  i  123 

mergella  124 

minuta  120 

nylanderi  122 

piscinalis  120,  121,  124 

sibirica  124 

simplex  (121),  122,  123 

sincera  122,  (123) 

striata  (123) 

tricarinata  120,  121,  122 

unicarinata  (i2t) 

virens  124 
Valvatidae  120 
Valvearius  (i2o) 
Velifera  36 
Velletia  (108),  109 
Velutinopsis  (61),  62,  65 
Vertigo  3,  2g 

approximans  (31) 

arctica  32 

arthuri  (31) 

binneyana  31 

bollesiana  (30) 

borealis  30 

callosa  (33) 

castanea  (29) 

Columbiana  30 

elatior  (31) 

gouldii  30 

hoppii  29, 

krauseana  32 

lagganensis  (31) 

milium  32,  33 

modesta  2g 

ovata  ^i,  32 

parietalis  (29) 

pentodon  (28) 

pygmaeajj 

simplex  (54) 

ventricosa  31 
Vertilla  milium  (32),  33 
Vesica  (59) 
Vitrea  38,  (40) 

binneyana  3g 


250 


INDEX 


Vitrea  fulva  (41) 
indentata  jp 
nitidula  3g 
radiatula  38 

Vitrinajj,  (36),  37 
alaskana  37,  38 
americana  (37) 
angelicse  36,  37 
beryllina  37 
bicolor  36 
conoidea  36 
diaphana  36 
exilis  (37).  j5 
lederi  36 
limpida  J7 
major  36 
paulucciae  36 
pellucida  36,  (37) 
pfeifferi  (37) 

Vitrinozonites  36 

Vitrinus  (35) 

Vivipara  11 

Viviparidae  124 

Vortex  81 


Vorticifex  63 

Zagrabica  (61),  65 

brusiniana  65 

naticoides  61 
Zonites  (39) 

conspectus  (53) 

fulvus  (40) 

lansingi  44 

nitidulus  (39) 

stearnsii  (44) 

viridulus  (38),  39 
Zonitidae  35 
Zonitoides  42 

arboreus  42 

milium  (43) 

minusculus  43 

nitidus  42 

pugetensis  43 

randolphi  43 
Zottgenites  21 

harpa  12,  21,  22,  I2» 
Zua  lubrica  (33) 

lubricoidea  (33) 
Zurama  (22) 


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