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status  and  Conservation  Management  of 
Terrestrial  Mollusks  of  Special  Concern 

in  Montana 


Prepared  for: 
The  U.S.  Forest  Service 


By: 
Paul  Hendricks 


Montana  Natural  Heritage  Program 

Natural  Resource  Information  System 

Montana  State  Library 


June  2003 


MONTANA 


Natural  Heritage 
Ftogtam 


status  and  Conservation  Management  of 
Terrestrial  Mollusks  of  Special  Concern 

in  Montana 


Prepared  for: 
The  U.S.  Forest  Service 


Contract  Number: 
Ol-lA-11015600-64 


By: 
Paul  Hendricks 


MONTANA 


Natuial  Heritage 
Ptt^jtam 


^it  ^-^  MUSTAFA  j^S^ijk      yf>WTAHA 

^T^itate  If  jIV  Natural  Kesouice 

^  Library  *^jj^  Iniomiation  System 


©  2003  Montana  Natural  Heritage  Program 

P.O.  Box  20 1800  •  1515  East  Sixth  Avenue  •  Helena,  MT  59620-1800  •  406-444-5354 


The  preferred  citation  for  this  document  is: 

Hendricks,  P.  2003.  Status  and  Conservation  Management  of  Terrestrial  MoUusks  of  Special  Concern 
inMontana.  Report  to  Region  I,  U.S.  Forest  Service.  Montana  Natural  Heritage  Program, 
Helena.  67  pp.  +  appendicies. 


EXECUTIVE  SUMMARY 

This  document  presents  information  on  the  distribution  and  status  of  1 5  terrestrial  moUusk  taxa  (species 
and  subspecies)  of  conservation  concern  in  Montana  that  have  been  found  on  or  near  lands 
administered  by  the  Northern  Region  (Region  1 ),  U.  S .  Forest  Service.  Included  in  this  group  are  ten 
snail  taxa  and  five  slug  taxa.  Each  species  or  subspecies  is  on  the  current  joint  Montana  Natural 
Heritage  Program  and  Montana  Fish,  Wildlife  and  Parks  Animal  Species  of  Concern  list  (Carlson 
2003),  as  either  a  Species  of  Concern  (eight  snail  and  three  slug  taxa)  or  On  Review  (two  snail  and  one 
slug  taxa);  one  slug  species  On  Review  (Udosarx  lyrata)  includes  a  subspecies  {U.  I  russelli)  that  is  a 
Species  of  Concern. 

Montana  is  the  type  locality  (where  the  species  or  subspecies  was  first  discovered  and  upon  which  the 
formal  description  is  based)  for  ten  of  the  moUusk  taxa  discussed  in  this  report.  A  review  of  available 
literature  and  unpublished  reports,  museum  records,  personal  discussions  and  correspondence,  and  field 
survey  results  provided  only  66  locality  records  for  all  species  and  subspecies  combined.  No  species 
has  been  reported  in  Montana  at  as  many  as  1 5  localities,  and  only  two  snails  have  been  documented  at 
as  many  as  ten  localities.  Two  snails  remain  known  from  single  localities  each  (the  type  localities),  and 
five  other  snails  and  slugs  from  two  to  four  localities  each.  To  date  (2002),  terrestrial  moUusks  of 
conservation  concern  have  been  found  on  or  near  seven  National  Forests  in  Montana:  Beaverhead- 
Deerlodge,  Bitterroot,  Flathead,  Gallatin,  Kootenai,  Lewis  and  Clark,  and  Lolo. 

Of  the  66  total  localities.  Heritage  Program  zoologists  discovered  nine  since  1 997,  and  two  additional 
localities  were  first  reported  in  200 1  by  other  biologists.  These  results,  obtained  largely  with  a  minimum 
of  survey  effort,  indicate  that  new  populations  for  several  of  the  species  of  conservation  concern  are 
possible,  even  likely.  However,  given  the  history  of  collecting  in  the  state  west  of  the  Continental  Divide, 
it  is  expected  that  most  of  the  moUusk  taxa  on  the  Heritage  list  will  remain  there,  although  their  global 
and  state  ranks  may  ultimately  be  downgraded. 

In  this  report,  species  accounts  for  each  taxon  are  provided  that  include  details  of  taxonomy  and  species 
identification,  life  history  and  ecology  notes,  a  distribution  map,  and  comments  on  status,  potential 
threats,  and  land  ownership  at  documented  (historical  and  recent)  locations.  Appendices  include  a 
summary  of  all  location  and  museum  collection  information,  guidelines  for  conducting  surveys  and 
inventories  of  terrestrial  moUusks,  and  a  key  to  the  genera  of  terrestrial  moUusks  in  Montana.  It  is 
hoped  that  this  document  will  1 )  bring  to  the  attention  of  Forest  Service  biologists  the  existence  of  a 
group  of  small  animals  of  conservation  concern  that  inhabit  or  may  inhabit  lands  under  their  stewardship, 
and  2)  help  Forest  Service  biologists  design  and  conduct  forest  inventories  for  these  species.  The 
ultimate  goal  of  this  document  is  to  assure  the  long-term  conservation  of  these  species  by  having  their 
needs  addressed  in  forest  plans. 


TABLE  OF  CONTENTS 

Acknowledgments iv 

Introduction 1 

Species  Accounts 

Snails 

Discus  brunsoni 9 

Discus  shimeki 13 

Oreohelix  alpina 17 

Oreohelix  amariradix 21 

Oreohelix  carinifera 25 

Oreohelix  elrodi 29 

Oreohelix  strigosa  berryi 33 

Oreohelix  yavapai  mariae 37 

Slugs 

Hemphillia  danielsi 41 

Magnipelta  mycophaga 45 

Zacoleus  idahoensis 49 

Species  on  Review 

Snails 

Polygyrellapolygyrella 53 

Radiodiscus  abietum 57 

Slugs 

Udosarx  lyrata 61 

Bibliography 64 

Appendix  A.  Global/State  Rank  Definitions 

Appendix  B.  Locality  and  Collection  Records  for  1 5  Terrestrial  MoUusk  Taxa  of  Conservation 

Concern  in  Montana 
Appendix  C.  Guidelines  for  Designing  and  Conducting  Surveys  of  Terrestrial  MoUusks 
Appendix  D.  Key  to  the  Genera  of  Terrestrial  MoUusks  of  Montana 


ACKNOWLEDGMENTS 

I  am  particularly  grateful  to  Fred  Samson  (USDA  Forest  Service)  for  recognizing  invertebrates  as  part 
of  the  native  fauna  inhabiting  The  Northern  Region,  and  concluding  there  is  a  need  to  address  the 
conservation  issues  invertebrates  confront.  John  Carlson,  Montana  Natural  Heritage  Program 
(MTNHP)  Lead  Zoologist,  was  instrumental  in  seeing  solidified  the  agreement  between  the  U.S.  Forest 
Service  and  MTNHP  to  develop  this  document. 

Information  gathered  here  was  assembled  from  published  literature,  unpublished  reports,  field  surveys, 
museum  collections,  and  personal  communications  with  agency,  academic,  and  private-sector  biologists. 
I  am  grateful  to  the  moUusk  collection  managers  of  the  California  Academy  of  Sciences  (CAS),  the 
Academy  of  Natural  Sciences  of  Philadelphia  (ANSP),  the  Field  Museum  of  Natural  History  of  Chi- 
cago (FMNH),  and  the  U.S.  National  Museum  (USNM)  for  providing  museum  records.  I  also  extend 
thanks  to  Lee  Fairbanks,  Terry  Frest,  Bill  Hammer,  Bill  Leonard,  Tom  Burke,  Heike  Reise,  and  Bryce 
Maxell  for  providing  specimen  records,  advice,  or  both.  Bill  Leonard  was  also  generous  in  sharing  his 
photographs  of  several  slug  species. 

For  help  in  the  production  of  this  report,  I  thank  Anne  Dalton  and  Terrie  Kenney  for  scanning  photo- 
graphs, Martin  Miller  for  entry  of  location  data  into  the  MTNHP  databases,  Whitney  Weber  for  map 
production  and  Cobum  Currier  for  report  formatting  and  production,  and  John  Carlson  for  feedback, 
advice,  and  comments  on  earlier  drafts  of  the  report.  All  are,  or  were,  fellow  employees  of  the 
MTNHP 

Finally,  I  express  my  thanks  to  Dr.  Royal  Bruce  Brunson  (deceased).  Emeritus  Professor  of  the  Depart- 
ment of  Zoology,  University  of  Montana  and  mid-twentieth  century  student  of  Montana's  moUusk  fauna, 
for  sharing  his  knowledge  and  providing  enthusiastic  support  of  my  novice  attempts  to  rediscover  what 
was  known  decades  before.  This  report  is  dedicated  to  him. 


N 


INTRODUCTION 

Background.  This  document  is  intended  to  serve  as  a  concise  summary  of  current  knowledge 
on  the  status,  distribution,  Ufe  history,  and  ecology  of  terrestrial  mollusks  (slugs  and  snails) 
determined  by  the  Montana  Natural  Heritage  Program  to  merit  state  Species  of  Concern  or  On 
Review  designation  (see  Carlson  2003).  The  information  gathered  has  been  used  to  1)  identify 
real  and  potential  threats  to  terrestrial  mollusks  of  conservation  concern  that  may  occur  on  U.S. 
Forest  Service,  Northern  Region  lands  in  Montana,  and  2)  develop  guidelines  for  field  surveys 
and  monitoring  schemes  on  Forest  Service  units  for  terrestrial  mollusks  of  conservation  concern. 
The  project  is  a  joint  venture  of  the  U.S.  Forest  Service,  Northern  Region  with  the  Montana 
Natural  Heritage  Program. 

Species  and  subspecies  in  this  document  (Table  1)  are  included  on  the  joint  Montana  Natural 
Heritage  Program/Montana  Department  of  Fish,  Wildlife  &  Parks  list  of  Animal  Species  of 
Concern  (Carlson  2003).  They  were  so  listed  based  on  information  and  recommendations  in 
Frest  and  Johannes  (1993,  1995)  for  species  occurring  in  the  Interior  Columbia  River  Basin  and 
the  Black  Hills  of  South  Dakota  and  Wyoming  (the  Black  Hills  region  includes  two  species  of 
concern  that  also  are  present  in  Montana);  several  species  included  are  covered  in  the  Columbia 
River  Basin  invertebrate  assessment  report  (Niwa  et  al.  2001),  where  listing  is  also 
recommended.  Montana  is  the  type  locality  (where  the  species  or  subspecies  was  first 
discovered  and  upon  which  the  formal  description  is  based)  for  10  of  these  taxa  (see  Appendix 
B). 

Table  1.  Terrestrial  snail  and  slug  Species  Of  Concern  or  On  Review  in  Montana  (Carlson  2003).  An  asterisk  (*) 
following  a  scientific  name  indicates  the  species  was  recommended  for  listing  in  the  Columbia  River  Basin 
invertebrate  assessment  report  (Niwa  et  al.  2001). 


Scientific  Name 

Common  Name 

Heritage  Rank^ 

Heritage  Category 

Snails 

Discus  brums oni"^ 

Mission  Range  Disc 

GlSl 

Concern 

Discus  shimeki 

Striate  Disc 

G4S1 

Concern 

Oreohelix  alpina'' 

Alpine  Mountainshell 

GlSl 

Concern 

Oreohelix  amariradix^ 

Bitterroot  Mountainshell 

G1G2S1S2 

Concern 

Oreohelix  carinifera^ 

Keeled  Mountainshell 

GlSl 

Concern 

Oreohelix  elrodi^ 

Carinate  Mountainshell 

GlSl 

Concern 

Oreohelix  strigosa  berryi 

Berry's  Mountainshell 

G5T2S1S2 

Concern 

Oreohelix  yavapai  mariae 

Gallatin  Mountainshell 

G4?T1  SI 

Concern 

Polygyrella  polygyrella 

Humped  Coin 

GUSU 

Review 

Radiodiscus  abietum 

Fir  Pinwheel 

GUSU 

Review 

Slugs 

Hemphillia  danielsi"^ 

Marbled  Jumping  Slug 

G1G3  S1S3 

Concern 

Magnipelta  mycophaga"^ 

Spotted  Slug 

G2G3  SI  S3 

Concern 

Udosarx  lyrata^^ 

Lyre  Mantleslug 

GUSU 

Review/Concern 

Zacoleus  idahoensis 

Sheathed  Slug 

G3G4  S2S3 

Concern 

^  G  =  Global  Rank,  S  =  State  Rank.  See  Appendix  A  for  definitions  of  abbreviations  and  ranks. 

^  A  described  subspecies,  Udosarx  lyrata  russelli  (Russell  Mantleslug),  is  ranked  G?T1  SI  and  placed  on  the 

Concern  list.  It  is  discussed  under  the  Lyre  Mantleslug  because  separate  treatment  is  not  justified  here.  Both  forms 

of  Udosarx  lyrata  were  recommended  for  listing  in  the  Columbia  River  Basin  invertebrate  assessment  report  (Nixa 

etal.2001). 


Although  the  two  reports  by  Frest  and  Johannes  form  the  basis  for  focus  of  mollusk  conservation 
in  Montana,  it  is  worth  noting  that  large  portions  of  Montana  still  await  evaluation  of  their 
molluscan  fauna.  The  Interior  Columbia  River  Basin  report  (Frest  and  Johannes  1995)  covers 
just  that  part  of  Montana  west  of  the  Continental  Divide  and  two  peripheral  species  of  concern; 
the  Black  Hills  report  (Frest  and  Johannes  1993)  does  not  cover  Montana  at  all,  but  discusses 
two  species  of  concern  present  also  in  Montana. 

A  Brief  History  of  Land  Mollusk  Faunal  Inventories  in  Montana.  Only  a  few  publications 
provide  accounts  of  the  extant  land  mollusk  faunas  in  Montana.  Elrod  (1902)  presented  the  first 
(and  apparently  only)  list  of  known  species  for  the  state,  while  recognizing  that  the  list  was 
necessarily  incomplete  due  to  inadequate  collecting  over  much  of  the  area,  a  problem  persisting 
to  this  day.  Elrod' s  (1902)  report  included  brief  mention  of  three  species  of  conservation 
concern  {Pyramidula  [=Oreohelix]  elrodi,  Pyramidula  [=Oreohelix]  alpina,  and  Polygyrella 
polygyrelld)  in  western  Montana,  and  included  the  records  of  Squyer  (1984)  from  the  Wibaux 
area  (known  as  Mingusville),  which  represented  essentially  the  only  information  from  the  eastern 
parts  of  Montana  at  that  time.  Shortly  thereafter.  Berry  (1916)  published  a  summary  of  his 
collecting  efforts  in  Meagher  and  Fergus  counties,  incorporating  his  earlier  and  briefer  report 
(Berry  1913)  and  including  an  account  of  Oreohelic  strigosa  berryi  in  the  Big  Snowy  Mountains. 
At  this  same  time,  Vanatta  (1914)  published  a  list  of  species  collected  by  L.  E.  Daniels  in  the 
Bitterroot  Mountains,  which  included  the  first  records  of  the  endemic  slug  Hemphillia  danielsi. 

Little  else  appeared  in  print  for  some  time,  until  Russell  and  Brunson  (1967)  compiled  what  was 
known  about  the  mollusk  fauna  of  Glacier  National  Park,  which  updated  an  earlier  report  by 
Berry  (1919)  and  included  many  new  observations  by  the  authors.  The  Russell  and  Brunson 
(1967)  list  is  probably  the  most  complete  for  any  area  of  significant  size  in  Montana. 
Interestingly,  none  of  the  land  mollusks  of  state  conservation  concern  have  been  documented  in 
Glacier  National  Park.  Unfortunately,  Brunson  (who  qualified  as  the  most  knowledgeable 
malacologist  residing  in  Montana  for  the  second  half  of  the  20*  Century)  never  wrote  a  revision 
of  Elrod' s  (1902)  out-dated  state  list,  even  though  several  additional  species  were  known  to 
occur  in  Montana  by  the  time  Brunson  retired  from  active  collecting  in  the  early  1980's. 

The  records  of  new  terrestrial  mollusk  species  and  locations  for  Montana,  including  several  of 
conservation  concern,  remain  scattered  in  publications  of  more  narrow  scope,  many  of  them  now 
decades  old  (e.g.,  Bartsch  1916,  Pilsbry  and  Brunson  1954,  Brunson  and  Osher  1957,  Brunson 
and  Russell  1967,  Fairbanks  1984),  or  deposited  as  vouchers  in  museum  collections  and 
otherwise  unpublished.  Fortunately,  most  or  all  of  the  species  of  greatest  conservation  interest  in 
Montana  are  discussed  in  Frest  and  Johannes  (1993,  1995)  as  part  of  mollusk  assessments  of  the 
Black  Hills  and  the  Interior  Columbia  River  Basin,  respectively.  Most  recently  (beginning  in 
1997),  additional  brief  surveys  for  a  few  species  have  been  made  by  Montana  Natural  Heritage 
Program  zoologists,  who  also  continue  to  solicit  and  accumulate  opportunistic  observations  of 
mollusks  for  the  Heritage  databases,  with  focus  on  species  of  conservation  concern  as  identified 
in  the  documents  of  Frest  and  Johannes  (1993,  1995). 


Distribution  and  Status  of  Species  of  Conservation  Concern.  A  review  of  available  literature 
and  unpublished  reports,  museum  records,  personal  discussions  and  field  survey  results  provided 
only  66  locality  records  (see  Appendix  B)  for  the  set  of  1 5  terrestrial  mollusk  taxa  of 
conservation  concern  listed  in  Table  1  (note  that  a  subspecies  of  slug,  Udosarx  lyrata  russelli,  is 
discussed  in  the  account  of  the  species).  Three  snails  {Discus  shimeki,  Oreohelix  strigosa  berryi, 
Oreohelix  yavapai  mariae)  are  known  from  sites  east  of  the  Continental  Divide;  the  remaining 
taxa,  including  all  of  the  listed  slugs,  are  known  only  from  sites  west  of  the  Continental  Divide. 
No  taxon  has  been  reported  in  Montana  at  as  many  as  15  total  localities,  and  only  two  {Oreohelix 
strigosa  berryi  and  Radiodiscus  abietum)  have  been  documented  at  as  many  as  ten.  Two  taxa 
{Discus  brunsoni  and  Oreohelix  yavapai  mariae)  remain  known  from  single  localities  each,  five 
others  {Oreohelix  alpina,  Oreohelix  amariradix,  Oreohelix  carinifera,  Oreohelix  elrodi,  and 
Udosarx  lyrata)  from  two  to  four  localities  each. 

All  but  one  terrestrial  mollusk  species,  the  Mission  Range  Disc  {Discus  brunsoni),  on  the  joint 
Montana  Natural  Heritage  Program-Montana  Department  of  Fish,  Wildlife  and  Parks  Animal 
Species  of  Concern  list  (Carlson  2003)  have  been  documented  on  or  near  at  least  one  National 
Forest  unit  in  the  Northern  Region  of  Montana  (Table  2).  Other  National  Forests  not  listed  in 
Table  2  are  likely  to  support  one  or  more  terrestrial  mollusk  species  of  conservation  concern, 
given  the  wide  distribution  of  some  of  these,  such  as  the  Striate  Disc  {Discus  shimeki)  and 
Berry's  Mountainshell  {Oreohelix  strigosa  berryi).  Many  of  the  listed  National  Forests  are  likely 
to  support  additional  taxa  of  conservation  concern  not  yet  documented  on  their  lands. 


Table  2.  Terrestrial  mollusk  Species  of  Concern  or  On  Review  (Carlson  2003)  that  have  been  documented  on 
National  Forest  lands  of  the  Northern  Region  (Region  1).  Species  in  brackets  ([  ])  indicate  a  species  that  has  been 
documented  <  2  km  from  a  particular  forest  boundary. 


Forest 

Mollusk  Species 

Beaverhead-Deerlodge 

Zacoleus  idahoensis 

Bitterroot 

Hemphillia  danielsi,  Radiodiscus  abietum,  Udosarx  lyrata 

Flathead 

Magnipelta  mycophaga,  Oreohelix  alpina,  Oreohelix  elrodi 

Gallatin 

Discus  shimeki,  Oreohelix  strigosa  berryi,  Oreohelix  yavapai  mariae 

Kootenai  (including  Kaniksu  in  Montana) 

Discus  shimeki,  Magnipelta  mycophaga,  Radiodiscus  abietum, 
Zacoleus  idahoensis 

Lewis  and  Clark 

Oreohelix  strigosa  berryi 

Lolo 

{Hemphillia  danielsi],  Magnipelta  mycophaga,  Oreohelix 
amariradix,  Oreohelix  carinifera,  Polygyrella polygyrella, 
Radiodiscus  abietum,  Zacoleus  idahoensis 

These  scant  results  lead  to  two  conclusions:  1)  most  species/subspecies  of  special  concern  are 
very  rare,  existing  in  small,  often  isolated  populations,  and  2)  survey  coverage  in  Montana  has 
been  woefully  inadequate  to  provide  a  reasonable  assessment  of  the  distribution  and  status  of 


most  or  all  taxa.  Field  surveys  and  opportunistic  observations  indicate  both  conclusions 
probably  are  reasonable.  With  very  limited  resources,  Heritage  Program  zoologists  have 
documented  four  priority  species  at  nine  new  localities  (of  the  66  total  localities  for  all  priority 
species)  since  1997,  and  determined  that  populations  of  three  species  remain  extant  at  five 
additional  localities  not  sampled  in  the  previous  30  years  (see  Appendix  B).  A  new  locality  (one 
of  three)  for  the  Carinate  Mountainshell  (Oreohelix  elrodi)  was  discovered  in  1999;  two  of  five 
total  Montana  localities  so  far  documented  for  the  Marbled  Jumping  Slug  {Hemphillia  danielsi) 
were  reported  first  in  2001  by  other  biologists.  Thus,  very  brief  field  surveys  and  opportunistic 
encounters  in  recent  years  have  significantly  increased  the  number  of  localities  where  terrestrial 
mollusks  of  conservation  concern  have  been  found.  Nonetheless,  some  species  (especially 
several  species  oi  Oreohelix  and  Discus  brunsoni)  have  been  the  focus  of  numerous  searches 
over  the  last  several  decades  (Frest  and  Johannes  1995,  R.  B.  Brunson  pers.  comm.)  with  few  or 
no  new  populations  discovered. 

Uncertainty  regarding  which  species  are  present  on  National  Forests  is  due  to  a  general  lack  of 
the  most  cursory  of  inventories  to  identify  the  terrestrial  mollusk  faunas  occupying  public  lands 
throughout  Montana.  Thus,  to  gauge  the  significance  of  federal  lands  for  maintaining  snails  and 
slugs  considered  rare  and  of  conservation  concern,  a  priority  should  be  placed  on  conducting 
field  surveys  of  appropriate  habitats  where  these  species  might  occur  on  National  Forests  of  the 
Northern  Region  (see  Appendix  C  for  guidelines).  The  evidence  from  recent  field  work 
indicates  additional  surveys  will  result  in  the  discovery  of  several  additional  populations  for 
some  species,  most  likely  the  slugs,  but  most  or  all  mollusk  species  currently  on  the  Species  of 
Concern  lists  (Carlson  2003)  probably  will  continue  to  be  identified  as  relatively  rare  and  of 
limited  distribution  in  Montana. 

The  discovery  of  new  locations  will  lead  to  a  reassessment  of  the  status  of  the  listed  species  in 
Montana  as  well  as  on  particular  National  Forests.  However,  species  new  to  the  known  mollusk 
fauna  of  Montana  are  still  possible.  As  an  example,  a  slug  species  "discovered"  (in  a  museum 
collection)  during  the  development  of  this  document,  the  Smokey  Taildropper  {Prophysaon 
humile)  (see  Frest  and  Johannes  1995),  not  yet  on  the  joint  Montana  Natural  Heritage 
Program/Fish,  Wildlife  &  Parks  list  of  "Animal  Species  of  Concern"  (Carlson  2003),  is  now 
known  to  be  present  in  Montana  (see  Appendix  C)  and  will  be  added  to  the  list  in  the  near  future 
because  it  is  of  conservation  concern  elsewhere  in  the  Interior  Columbia  River  Basin  (Frest  and 
Johannes  1995,  Niwa  et  al.  2001).  Thus,  with  additional  survey  documentation,  we  can  expect 
that  several  species  will  be  added  to  the  individual  National  Forest  lists,  including  some  that  may 
not  yet  be  known  to  occur  in  Montana.  But  with  continued  survey  effort  we  can  also  anticipate 
that  some  species  will  be  dropped  from  the  list  of  species  of  conservation  concern  in  Montana 
because  they  are  known  to  be  more  secure  than  their  current  ranks  indicate. 

Summary  of  Occupied  Habitats.  Generally  speaking,  the  15  terrestrial  mollusk  species  of 
conservation  interest  in  Montana  (Table  1)  fall  into  two  habitat  groupings:  1)  species  often 
associated  with  talus  or  rocky  outcrops  (Talus  Group),  and  2)  species  often  associated  with  moist 
valley  and  canyon  (ravine)  mixed-conifer  forests  (Moist  Forest  Group).  The  two  groupings  may 
overlap  in  some  cases;  some  of  the  moist  mix-conifer  forest  species  are  often  found  in  rocky 
sites,  and  the  talus-inhabiting  species  may  occupy  talus  imbedded  in  a  forested  landscape.  But 
the  microhabitats  where  these  two  groups  occur  are  usually  easy  to  differentiate. 


All  of  the  Oreohelix  species  listed  in  Table  1,  as  well  as  Discus  brunsoni,  associate  with  talus  or 
rocky  ground,  although  the  occupied  sites  may  range  from  low-elevation  canyons  and  valley 
bottoms  to  high-elevation  slopes  well  above  treeline.  Sites  occupied  by  this  group  are  typically 
in  terrain  that  is  more  open  and  mesic  than  where  the  second  group  associates.  Sites  occupied  by 
the  second  group  (the  four  slugs,  Discus  shimeki,  Polygyrella  polygyrella,  Radiodiscus  abietum) 
tend  to  be  near  permanent  water,  such  as  riparian  corridors,  and  in  dense  conifer  forests  where 
there  is  more  precipitation,  litter  and  decaying  wood.  This  group  of  species  also  frequents  areas 
with  a  deciduous  wood  component  of  species  such  as  aspen,  cottonwood,  alder  and  birch. 

Potential  Threats.  No  studies  exist  that  document  the  response  of  any  of  the  15  terrestrial 
mollusk  species  of  conservation  concern  to  disturbance.  Threats  to  populations  of  these  species 
is  largely  guess  work,  and  based  on  the  type  and  extent  of  habitat  alteration  and  disturbance  that 
has  occurred  in  Montana  in  the  last  century. 

Any  kind  of  habitat  alteration  that  reduces  the  humidity  of  the  microhabitats  where  these  species 
occur  is  a  potential  threat  to  both  groups,  but  probably  greatest  for  the  Moist  Forest  Group. 
Canopy  removal  through  logging  and  fire  are  probably  the  most  significant  disturbances  for  the 
forest-inhabiting  species;  historical  forest  clearing  has  likely  resulted  in  significant  reductions 
and  fragmentation  of  their  former  ranges.  Logging  and  fire  are  also  potentially  significant 
factors  of  disturbance  for  talus-inhabiting  species,  but  talus  occupied  by  these  species  may  be 
deep  enough  to  provide  necessary  humidity  and  temperature  regimes  that  will  protect  them  from 
logging  and  fire,  at  least  in  some  cases  and  in  the  short  term.  However,  construction  of  roads  to 
support  logging  operations  could  threaten  even  some  of  these  seemingly  protected  talus  sites. 

Grazing  has  the  potential  to  negatively  impact  both  groups,  but  some  of  the  species  inhabiting 
talus  (especially  Discus  brunsoni,  Oreohelix  alpina,  and  Oreohelix  elrodi)  are  probably  largely 
buffered  from  grazing  impacts  due  to  the  specific  types  of  rocky  terrain  they  occupy.  For  other 
species  in  more  expose  sites,  trampling  and  grazing  could  devastate  the  habitat  occupied  by  the 
snails  and  slugs,  removing  plant  cover  and  potential  food,  and  destabilizing  occupied  slopes. 
Rural  home  development  and  highway  and  road  maintenance  also  have  the  potential  to 
contribute  to  habitat  loss  for  several  species  in  both  groups  largely  restricted  to  low-elevation 
valleys  and  slopes  in  apparently  very  localized  populations  {Oreohelix  amariradix  and  Oreohelix 
carinifera  are  examples). 

Use  of  chemicals  for  controlling  noxious  weeds  could  present  land  managers  with  situations 
where  protection  of  rare  animal  species  is  balanced  against  the  need  to  control  or  eradicate  exotic 
pest  species,  and  special  effort  may  be  required  to  assure  the  protection  of  the  mollusks  during 
these  operations.  Several  of  the  mollusk  species  of  conservation  concern  probably  occupy  areas 
where  control  of  noxious  weeds  is  desirable,  especially  along  heavily  used  roads  and  trails. 
During  the  writing  of  this  report  it  was  discovered  through  conversation  with  Forest  Service 
personnel  that  a  weed  control  program  will  soon  occur  at  the  only  site  known  for  the  Gallatin 
Mountainsnail  (Oreohelix  yavapai  mariae),  A  survey  of  the  site  should  be  conducted  before 
spraying  to  identify  the  area  occupied  by  the  snails,  so  that  disturbance  to  this  rare  endemic  snail 
can  be  avoided.  Similar  situations  such  as  the  above  will  probably  occur  in  the  future  as  weed 
control  receives  more  emphasis.  This  further  underscores  the  need  for  new  surveys  to  identify 


sites  currently  occupied  by  the  terrestrial  moUusks  of  conservation  concern  discussed  in  this 
report. 

Summary  of  this  report.  The  species  accounts  that  follow  include  information  on  taxonomy 
and  species/subspecies  identification  (including  photographs  when  available),  life  history  notes 
on  reproductive  biology,  ecology  and  habitat  associations,  information  of  the  range-wide 
distribution  and  distribution  within  Montana  (including  distribution  maps),  current  abundance, 
potential  or  real  threats,  and  land  ownership  at  known  localities.  In  some  sections,  particularly 
threats  and  distributions,  what  is  written  is  too  often  speculation.  This  is  unavoidable  because  so 
little  is  known  of  these  topics  about  most  species  of  conservation  concern. 

A  bibliography  pertaining  to  the  species  of  conservation  concern,  which  includes  most  or  all  of 
the  published  and  gray  literature  mentioning  the  species  that  are  the  focus  of  this  report,  is 
included  at  the  end  of  the  individual  species  accounts.  A  table  summarizing  available  geo-spatial 
data  for  each  occurrence,  along  with  collection/observation  dates  and  museum  accession 
numbers,  as  well  as  available  habitat  information  briefly  noted,  is  provided  in  Appendix  B. 
Guidelines  for  designing  and  conducting  field  surveys  are  provided  in  Appendix  C.  A  key  to  the 
genera  of  terrestrial  Montana  mollusks  is  provided  in  Appendix  D  as  an  aid  to  field  workers 
encountering  snails  and  slugs  and  attempting  an  initial  determination  of  what  they  have  found.  It 
is  hoped  that  the  production  of  this  report  will  impress  upon  agency  and  private  sector  biologists 
the  magnitude  of  our  ignorance,  and  spur  them  to  take  measures  to  reduce  it. 


Figure  1.  Distribution  of  Discus  brunsoni  in  Montana. 


•     Discus  brunsoni 
^^/Continental  Divide 
US  Forest  Service 


(Mission  Range  Disc) 

■ 

ra 

-4 

^B?^h|'^-' 

\    - 

'■       1 

Wm .     ms^ 

SPECIES  ACCOUNTS 
SNAILS 


SPECIES:  Discus  brunsoni 
HeritageRank:Gl,Sl 
Natural  History 

A.  Taxonomy 

Family:  Discidae 

Discus  brunsoni  Berry,  1955 

Berry  (1 955)  described  this  distinctive  taxon  as  a  full  species.  There  remain  questions  regarding 
its  true  taxonomic  affinities,  but  complete  knowledge  will  not  affect  the  validity  as  a  full  species 
(see  Frest  and  Johannes  1 995). 

B.  Species  Description 

Morphology:  The  following  description  is  taken  from  Berry  (1 955).  "Shell  large  for  the  genus, 
thin,  depressed-conic,  with  low  spire,  its  slopes  weakly  convex.  Whorls  about  five  and  a  half, 
decidedly  compressed,  moderately  rounded  both  above  and  below  the  strongly  but  not  acutely 
carinate  periphery, . . . ;  base  fiattened,  the  widely  open  vorticiform  umbilicus  contained  about 
three  times  in  the  major  diameter  of  the  shell; . . .  Aperture  transversely  ovate,  compressed, . . . 
Color  near  olive-brown, ...  the  basal  surface  and  that  of  young  shells  tending  to  be  a  little 
brighter;  no  inherent  variegation  of  color  pattern  evident."  Maximum  diameter  of  holotype  10.5 
mm,  minimum  diameter  9. 1  mm;  height  of  shell  4.2  mm,  diameter  of  umbilicus  3.5  mm. 
Maximum  diameters  of  eight  live  individuals  measured  by  Hendricks  (1 998)  ranged  from  6.7 
mm  to  10.5  mm  (mean  =  9.5  +  1.4  mm). 

Reproductive  biology:  Hermaphroditic,  so  far  as  known.  Internal  anatomy  is  not  yet  described 
(Berry  1955,  Frest  and  Johannes  1 995),  and  there  are  no  descriptions  of  the  reproductive 
behavior  and  its  seasonal  occurrence.  Lifespan  is  unknown.  Age/size  at  maturity  is  unknown. 

Ecology:  Occupies  open,  south  facing  and  rather  dry  talus  slopes  with  very  low  canopy  cover. 
Vegetation  at  the  margins  of  the  talus  slopes  includes  Douglas-fir  (Pseudotsuga  menziesii\ 
ponderosa  pine  (Pinus  ponderosa),  pockets  of  water  birch  (Betula  occidentalis),  quaking 
aspen  (Populus  tremuloides),  and  mock  orange  {Philadelphus  lewisii).  Rock  composition  at 
the  type  locality  was  described  as  limestone  (Berry  1 955,  Frest  and  Johannes  1 995),  but  more 
recent  examination  (Hendricks  1 998)  revealed  the  occupied  talus  to  be  a  mix  of  diorite  and 
argillite  with  no  limestone  present.  Apparently  this  species  retreats  deep  into  the  talus  when 
surface  conditions  are  unfavorable.  Brunson  (1956)  suggested  that  D.  brunsoni  may  be 


crepuscular  or  nocturnal  near  the  surface,  because  many  collections  were  made  shortly  before 
dusk,  or  at  least  in  subdued  light,  following  intensive  mid-day  searches.  Hendricks  (1 998), 
however,  located  live  animals  at  the  surface  during  mid-day  when  ambient  surface  conditions 
were  overcast,  wet  and  cool.  Oreohelix  elrodi  is  also  present  in  the  occupied  talus.  Foods  are 
unknown,  but  it  may  feed  most  often  on  plant  material  on  rock  surfaces  (lichens,  etc.)  rather 
than  patches  of  accumulated  leaf  and  conifer  needle  litter  (Brunson  1 956,  Hendricks  1 998). 

C.  Range  and  Known  Sites 

Discus  brunsoni  is  known  only  from  the  Mission  Mountains  in  Lake  County,  northwestern 
Montana  (Fig.  1 ,  Appendix  B).  The  type  locality  is  the  south-facing  slope  above  McDonald 
Lake  in  the  Mission  Mountains  Tribal  Wilderness  of  the  Confederated  Salish  and  Kootenai 
Tribes,  at  about  1 120  m  (3700  ft)  elevation.  Several  talus  slopes  are  present  above  the  north 
shore  of  the  lake;  Brunson  (1 956)  indicates  more  than  one  slope  is  occupied,  but  Hendricks 
(1 998)  found  D.  brunsoni  only  in  the  talus  slope  where  diorite  was  abundant. 

To  date,  the  type  locality  is  the  only  location  where  D.  brunsoni  has  been  found.  Over  70 
specimens  of  this  species  have  been  uncovered  in  seven  different  years  since  the  first  shell  was 
found  in  August  1 948;  the  most  recent  known  observation  was  in  July  1 997  (Hendricks  1 998). 

D.  Species  Abundance 

Discus  brunsoni  is  a  local  endemic,  perhaps  present  only  in  the  Mission  Mountains.  Because 
the  species  occupies  large  and  deep  talus  slopes  it  is  difficult  to  make  estimates  of  population 
size.  During  favorable  surface  conditions,  Hendricks  (1 998)  found  it  to  be  much  less  abundant 
near  the  surface  than  sympatric  Oreohelix  elrodi,  another  regional  endemic  of  conservation 
concern. 

Current  Status 

A.  Why  Species  is  of  Conservation  Concern 

The  Mission  Range  Disc  {Discus  brunsoni)  is  a  Species  of  Concern  in  Montana  because  it  is  a 
local  endemic  so  far  documented  at  a  single  site,  despite  several  decades  of  widespread 
collecting  in  the  region  by  Dr.  R.  B.  Brunson  and  students  (Frest  and  Johannes  1 995,  Brunson 
personal  communication).  Population  size  and  trends  are  unknown.  Recommended  for  Federal 
listing  by  Frest  and  Johannes  (1 995). 

B.  Threats 

Although  the  occupied  habitat  is  not  particularly  threatened  by  development  or  agriculture 
(logging  and  grazing),  habitat  requirements  and  food  habits  are  poorly  understood.  Fire 
suppression  efforts  (especially  use  of  fire  retardants)  and  talus  destabilization  (trail  maintenance, 
modification)  could  have  negative  impacts.  Also,  given  the  trail-side  location,  weed  control 
efforts  could  negatively  impact  the  population. 


10 


C.  Distribution  Relative  to  Land  Allocations 

The  only  known  occupied  site  is  in  the  Confederated  Sahsh  and  Kootenai  Tribes  Mission 
Mountains  Tribal  Wilderness.  Amajor  hiking  and  packing  trail  bisects  the  site.  Additional 
populations  associated  with  diorite  and  argillite  talus  may  be  present  elsewhere  in  the  Mission 
Mountains  on  tribal  and  national  forest  lands.  There  are  quartz  diorite  outcrops  that  should  be 
surveyed  in  the  North  Fork  and  South  Fork  of  Elk  Creek  drainages  in  the  Flathead  National 
Forest,  and  near  the  Crow  Creek  Lakes  in  the  Mission  Mountains  Tribal  Wilderness. 


11 


Figure  2.  Distribution  of  Discus  shimeki     in  Montana. 


•     Discus  shimeki 
^^/Continental  Divide 
US  Forest  Service 


12 


SPECIES:  Discus  shimeki  (Striate  Disc) 

Heritage  Rank:  G4,S1 
Natural  History 

A.  Taxonomy 

Family:  Discidae 

Discus  shimeki  (Pilsbry,  1 890) 

Originally  described  from  fossil  material  in  Peoria  Loess  in  Iowa.  The  extant  western 
subspecies,  D.  s.  cockerelli,  is  considered  by  some  authorities  to  be  indistinguishable  from  the 
nominate  form  (Frest  and  Johannes  1 993). 

B.  Species  Description 

Morphology:  The  following  description  is  from  Pilsbry  (1 948).  "The  whorls  are  much  more 
robust  than  D.  cronkhitei.  It  has  a  low  conic  spire,  rounded  periphery  and  rather  narrowly 
umbilicate  base,  the  umbilicus  contained  about  3 .7  to  4  times  in  the  diameter.  The  first  whorl 
projects  somewhat,  the  first  1 V2  whorls  smooth;  following  whorls  regularly  and  rather  strongly 
rib-striate,  . . .  [the  ribs]  become  somewhat  lower  and  irregular  on  the  last  whorl,  where  they 
disappear  in  the  peripheral  region,  the  base  being  marked  only  with  weak  wrinkles  of  growth." 
This  snail  differs  from  the  sympatric  Discus  cronkhitei  (=  whitneyi)  by  its  smoother  base  and 
weaker  ribs  on  the  last  whorl.  The  shell  is  thin,  and  brownish  in  color.  Height  is  about  3 .7  mm, 
maximum  diameter  about  6-7  mm;  4.5  whorls. 

Reproductive  biology:  Hermaphroditic.  Copulation  observed  in  March- June.  Egg  laying  occurs 
from  April- August  in  the  Black  Hills;  clutch  size  is  relatively  small  (3-6).  Apparently  most 
members  of  this  species  have  a  one-year  life  cycle  (Frest  and  Johannes  1993).  Age/size  at 
reproductive  maturity  has  not  been  described. 

Ecology:  This  species  tends  to  associate  with  quaking  aspen  (Populus  tremuloides)  at  Montana 
sites  where  habitat  was  documented  (Hendricks  unpublished  data).  Elsewhere  in  the  Rocky 
Mountains  it  is  also  associated  with  spruce  (Picea)  and  fir  (Abies)  intermixed  with  aspen  or 
other  broadleaf  trees  and  shrubs  (Beetle  1957, 1997,  Karlin  1961,  Frest  and  Johannes  1993). 
Soils  often  are  derived  from  weathering  limestone.  D.  shimeki  is  active  most  often  in  litter  in 
lowland  forest,  but  sometimes  is  seen  on  downed  wood  and  rock  surfaces.  Slopes  are  often 
north-facing  and  shaded.  This  species  appears  to  subsist  largely  on  decaying  deciduous  leaves. 

C.  Range  and  Known  Sites 

Discus  shimeki  is  widely  distributed  in  the  Rocky  Mountains  of  Arizona,  New  Mexico,  Utah, 
Colorado,  and  Wyoming,  with  populations  also  extant  in  the  Black  Hills  (Frest  and  Johannes 
1 993).  It  is  also  found  north  of  Montana  in  the  Canadian  Rockies  (Piatt  1 980).  Pilsbry  (1 948) 


13 


lists  only  one  Montana  location  for  this  species,  along  the  Boulder  River  in  Sweetgrass  County 
(also  referenced  in  Frest  and  Johannes  1 993).  The  species  has  been  documented  in  Montana 
(Fig.  2,  Appendix  B)  in  five  counties  total  (Gallatin,  Hill,  Lincoln,  Park,  Sweetgrass),  at 
elevations  ranging  from  640  m  (2 1 00  ft)  to  1 940  m  (63  60  ft) .  The  most  recent  records  are 
from  along  Beaver  Creek  in  the  Bears  Paw  Mountains,  Hill  County  (1 997)  and  west  of  Nurses 
Lakes  (Gallatin  National  Forest)  in  the  Absaroka  Mountains,  Park  County  (2001). 

D.  Species  Abundance 

Population  sizes  are  not  reported.  The  species  can  be  abundant  in  colonies,  but  colony  sites  are 
relatively  small  in  extent  (Frest  and  Johannes  1 993).  At  some  sites  where  the  species  has  been 
documented  in  Montana,  D.  shimeki  is  less  abundant  than  D.  cronkhitei  (=whitneyi)  (pers. 
obs.). 

Current  Status 

A.  Why  Species  is  of  Conservation  Concern 

The  Striate  Disc  {Discus  shimeki)  is  a  Species  of  Concern  in  Montana  because  of  the  limited 
number  of  sites  where  it  has  been  documented  in  the  state,  despite  several  decades  of 
widespread  collecting  in  the  region  by  Dr.  R.  B.  Brunson  and  students  (Frest  and  Johannes 
1 993, 1 995).  Recommended  for  Federal  listing  by  Frest  and  Johannes  (1 993). 

B.  Threats 

Major  threats  to  known  sites  include  degradation  due  to  timber  harvest  and  livestock  grazing, 
with  the  latter  likely  the  main  threat.  Fire  is  also  a  concern;  stand  replacement  fires  could 
permanently  eliminate  populations  in  isolated  colonies  (see  Beetle  1 997).  Response  of  snails  to 
fire  retardants  has  not  been  studied. 

C.  Distribution  Relative  to  Land  Allocations 

Known  sites  in  Montana  include  Forest  Service  and  Tribal  lands  at  widely  separated  locations. 
Addition  sites  are  possible  on  these  as  well  as  private  lands  throughout  the  montane  regions  of 
Montana,  including  some  of  the  island  mountain  ranges  in  the  prairie  regions  east  of  the  main 
Rocky  Mountain  chain.  None  of  the  sites  has  special  protection. 


14 


Figures.  Distribution  of   Oreohelix alpina    in  Montana. 


•     Oreohelix  alpina 
^^/Continental  Divide 
US  Forest  Service 


16 


SPECIES:  Oreohelix  alpina 

HeritageRank:Gl,Sl 

Natural  History 

A.  Taxonomy 

Family:  Oreohelicidae 
Oreohelix  alpina  (Elrod,  1901) 


(Alpine  Mountainsnail) 


Originally  named  Pyramidula  strigosa  alpina  by  Elrod  (1 90 1  a,  1 903b).  Pilsbry  (1 939) 
expressed  some  doubt  about  the  validity  of  this  taxon,  but  later  examination  of  material  by  Frest 
and  Johannes  (1995)  and  Fairbanks  (2002)  indicate  treatment  as  a  full  species  is  appropriate. 
Pilsbry  (1 933)  placed  Oreohelix  alpina  with  the  O.  strigosa  group,  as  did  Elrod  (1 901  a, 
1 902, 1 903b),  but  later  (Pilsbry  1 939)  moved  it  to  the  O.  subrudis  group.  Recent  study  of  the 
internal  anatomy  (Fairbanks  2002)  indicates  affinity  with  the  O.  strigosa  group.  Pilsbry  (1 939) 
placed  all  Oreohelix  in  the  Xanthonycidae. 

B.  Species  Description 

Morphology :  Descriptions  of  shells  from  the  Mission  Mountains  are  provided  in  Elrod  (1901, 
1902, 1903b),  Pilsbry  (1939),  Hendricks  (1998),  and  Fairbanks  (2002);  reproductive  anatomy 
is  described  in  Fairbanks  (2002).  Description  from  Pilsbry  (1 939)  follows:  "shell  small; 
brownish-gray,  tending  toward  light  hom  color,  in  dead  shells  tuming  to  pearly  white;  luster 
somewhat  silky;  shell  flat,  little  elevated; . . .  aperture  nearly  circular, . . .  somewhat  higher  than 
wide;  markings  as  in  strigosa,  the  upper  band  continuing  in  the  spire,  gradually  disappearing; 
umbilicus  medium,  circular,  deep,  subcylindric."  Shell  diameter  7-10  mm,  average  often 
specimens,  8.91  mm,  shell  height  3-5mm,  whorls  4.0-4.5.  Hendricks  (1998)  reported  range  in 
diameter  of  1 6  live  shells  =  2.5-8.5  mm,  nine  dead  shells  =  8.0-9.6  mm.  Shells  from  the  Swan 
Range  may  average  slightly  larger  in  diameter:  average  of  1 3  was  9.4  mm,  range  5.7-11.4  mm 
(Hendricks  unpublished  data);  average  of  four  was  9.3  mm,  range  8.5-11 . 1  mm  (Fairbanks 
2002). 

Reproductive  biology:  Hermaphroditic;  reproductive  anatomy  described  in  Fairbanks  (2002). 
There  are  no  descriptions  of  reproductive  behavior  and  its  seasonal  occurrence.  Lifespan  is 
unknown.  Age/size  at  reproductive  maturity  is  unknown. 

Ecology:  Occupies  open  talus  slopes  at  high  elevations  near  and  above  treeline  (Elrod  1 902, 
1 903b,  Hendricks  1 998).  Vegetation  at  and  near  the  alpine  type  locality  on  East  St.  Marys 
Peak  in  the  Mission  Mountains  (Hendricks  1 998)  includes  the  wild  flowers  snow  cinquefoil 
(Potentilla  nivea),  mountain  avens  (Dryas  octopetala),  alpine  sorrel  (Oxyria  digyna)  and 
moss  campion  (Silene  acaulis).  Subalpine  fir  {Abies  lasiocarpa)  is  present  at  the  margins  of 
the  subalpine  site  above  Lower  Rumble  Lake  in  the  Swan  Range  (Hendricks  unpublished  data). 
Rock  substrate  at  all  known  sites  is  limestone.  Live  shells  are  found  on  surfaces  of  limestone 


17 


blocks,  but  often  in  the  absence  of  direct  sunlight  (shaded  areas  and  undersides  of  smaller 
blocks).  Block  size  where  O.  alpina  was  found  on  St  Marys  Peak  averaged  20  x  30  cm 
square  and  4-8  cm  thick  (Hendricks  1 998),  block  size  at  the  Swan  Range  site  ranged  from  1 5  x 
1 5  X  4  cm  to  1  m^  (Hendricks  unpublished  data).  Some  soil  development  and  leaf  litter  was 
present  at  each  site  where  live  snails  were  found;  one  group  of  live  snails  was  found  in  leaf  litter 
near  the  base  of  snow  cinquefoil  partially  protected  overhead  by  rock.  Food  habits  are 
unknown. 

C.  Range  and  Known  Sites 

Oreohelix  alpina  is  known  from  three  sites  (Fig.  3,  Appendix  B)  in  two  counties  (Elrod  1 902, 
1 903b,  Hendricks  1 998,  Fairbanks  2002).  The  type  locality  is  East  St.  Marys  Peak  in  the 
Mission  Mountains  of  Lake  County,  from  2710m  (8900  ft)  to  2865  m  (9400  ft)  elevation.  The 
second  site  in  the  Mission  Mountains  is  more  extensive,  and  includes  West  McDonald  Peak,  the 
summit  area  of  McDonald  Peak,  and  the  slopes  of  McDonald  Peak  above  Duncan  Lake,  all  in 
Lake  County,  from  2255  m  (7400  ft)  to  2957  m  (9700  ft)  elevation.  The  third  site  is  above 
Lower  Rumble  Lake  in  the  Swan  Range,  Missoula  County,  at  21 95  m  (7200  ft)  elevation. 

The  known  sites  have  been  visited  infrequently,  probably  because  of  difficult  access.  Prior  to 
1 997,  the  species  had  not  been  reported  at  either  Mission  Mountains  site  since  1 952  (specimen 
in  the  Field  Museum  of  Natural  History,  Chicago),  and  there  remain  few  collections  of  this 
species.  The  Swan  Range  site  was  not  discovered  until  1 975,  and  O.  alpina  had  not  been 
documented  again  at  this  locality  until  2000.  Other  sites  within  each  mountain  range  are  likely  to 
exist.  Additional  populations  may  be  discovered  in  portions  of  the  Bob  Marshall  Wilderness. 

D.  Species  Abundance 

Oreohelix  alpina  is  a  local  endemic  restricted  to  the  Mission  Mountains  and  nearby  Swan 
Range.  The  species  was  relatively  abundant  at  some  locations  within  sites  of  occurrence  (Elrod 
1 902,  Hendricks  1 998).  However,  no  population  estimates  are  available,  and  nothing  is  known 
regarding  population  trends  at  any  site. 

Current  Status 

A.  Why  Species  is  of  Conservation  Concern 

The  Alpine  Mountainshell  {Oreohelix  alpina)  is  a  Species  of  Concern  in  Montana  because  it  is 
a  local  endemic  so  far  documented  at  three  sites,  despite  several  decades  of  widespread 
collecting  in  the  region  by  Dr.  R.  B.  Brunson  and  students  (Frest  and  Johannes  1 995). 
Population  size  and  trends  are  unknown.  Recommended  for  Federal  listing  by  Frest  and 
Johannes  (1995). 


18 


C.  Threats 

Occupied  habitat  (alpine  and  high-elevation  limestone  talus)  is  not  threatened  by  current  land 
use  practices.  Probably  the  greatest  threat  to  species  persistence  is  climate  change. 

C.  Distribution  Relative  to  Land  Allocations 

The  two  known  sites  in  the  Mission  Mountains  are  in  the  Confederated  Salish  and  Kootenai 
Tribes  Mission  Mountains  Tribal  Wilderness.  The  Swan  Range  site  is  on  the  Flathead  National 
Forest  (Swan  Lake  Ranger  District).  Additional  populations  are  possible  on  adjacent  Tribal  and 
Forest  Service  lands. 


19 


Figure  4.  Distribution  of   Oreohelix  amariradix    in  Montana. 


•     Oreohelix  amariradix 
^^/Continental  Divide 
US  Forest  Service 


20 


SPECIES:  Oreohelix  amariradix  (Bitterroot Mountainsnail) 

Heritage  Rank:  G1G2,  S1S2 
Natural  History 

A.  Taxonomy 

Family:  Oreohelicidae 

Oreohelix  amariradix  Pilsbry,  1 934 

Originally  identified  by  Elrod  ( 1 90 1  a,  1 902, 1 903b)  as  a  "small  variety"  of  Oreohelix 
(=Pyramidula)  strigosa  from  the  Bitterroot  Mountains,  but  described  by  Pilsbry  (1 933)  as  a 
full  species  of  the  O.  strigosa  group,  based  only  on  dead  shells.  Fairbanks'  (1980)  analysis  of 
the  internal  anatomy  confirmed  Pilsbry 's  designation.  Pilsbry  (1 939)  placed  all  Oreohelix  in  the 
Xanthonycidae. 

B.  Species  Description 

Morphology:  Pilsbry  (1 933, 1 939)  describe  the  shell  as  "openly  umbilicate,  the  umbilicus 
contained  about  4  times  in  the  diameter;  biconvex  with  the  periphery  rather  sharply  angular,  the 
angle  disappearing  on  the  last  third  of  a  whorl.  Whorls  51/3,  the  embryonic  21/3  moderately 
convex  and  nearly  smooth.  Susequent  whorls  rather  coarsely  and  irregularly  wrinkle-striate, 
without  spiral  striation,  but  there  is  often  a  spiral  impression  above  the  suture  on  the  penult 
whorl.  The  last  whorl  descends  shortly  in  front.  Aperture  rather  strongly  oblique, . . .  The 
specimens . . .  show  a  reddish  band  immediately  below  the  periphery,  another  a  short  distance 
above  it."  Shell  height  8.5  mm,  diameter  14.5  mm.  Elrod  (1 903b)  gives  height  of  1 0  shells  5.3- 
7.4  mm,  diameter  1 1 .9-16.7  mm;  number  of  whorls  4.8-5.4.  Fairbanks  (1980)  gives  height  of 
6.9-10.9  mm  and  diameter  of  1 2.8- 1 7.9  mm  for  2 1  specimens  from  another  site  nearby; 
number  of  whorls  4.75-5.5. 

Reproductive  biology:  Hermaphroditic  (Fairbanks  1980).  No  description  of  reproductive 
behavior  and  its  seasonal  occurrence  in  natural  settings.  Life  span  is  unknown.  Age/size  of 
reproductive  maturity  is  not  described;  in  captivity  young  bom  live  after  adults  overwintered. 

Ecology:  This  species  occupies  small  talus  slides,  primarily  the  basal  portions  (Frest  and 
Johannes  1995),  scattered  among  open  grassy,  south-facing  slopes  that  become  quite  dry  in 
mid-summer  (Elrod  1903b,  Fairbanks  1980).  Vegetation  at  one  site  included  bunch  grasses, 
ponderosapine  {Pinus  ponderosa),  serviceberry  (Amelanchier  alnifolia),  and  ninebark 
(Physocarpus  malvaceus).  Food  habits  are  unknown. 

C.  Range  and  Known  Sites 

Oreohelix  amariradix  is  known  only  from  the  Lolo  Creek  drainage  near  Fort  Fizzle,  Missoula 
County  (Fig.  4,  Appendix  B)  at  about  1 070  m  (3500  ft)  elevation.  Elrod  (1 903b)  gave  the 


21 


elevation  at  the  type  locality  as  1 524  m  (5000  ft),  but  this  is  likely  an  error,  as  Lolo  Pass  is  < 
100  m  elevation  above  this  contour,  nor  does  habitat  at  that  elevation  fit  the  description. 
Reported  records  along  the  Clark  Fork  River  at  Ravenna  and  Nimrod  (Frest  and  Johannes 
1 995)  appear  to  be  an  error,  perhaps  confiised  with  locations  for  O.  carinifera  (see  next 
species  account),  as  no  documentation  was  found  for  O.  amariradix  at  these  sites. 

The  known  sites  have  been  visited  infrequently.  Attempts  by  Frest  and  Johannes  (1 995)  to 
locate  living  animals  in  1 994  were  unsuccessful,  although  these  authors  state  that  the  species  is 
extant  at  two  Lolo  Creek  drainage  sites.  Given  their  comments,  and  earlier  ones  by  Elrod 
(1901),  populations  other  than  those  listed  in  Appendix  B  may  exist  in  the  Lolo  Creek  area. 

D.  Species  Abundance 

Oreohelix  amariradix  is  a  local  endemic  restricted  to  the  Bitteroot  Mountains.  There  are  no 
published  estimates  of  population  size  or  relative  abundance.  There  may  be  an  overall  declining 
trend  in  absolute  abundance,  given  Frest  and  Johannes'  (1 995)  comments  about  local 
extinctions. 

Current  Status 

A.  Why  Species  is  of  Conservation  Concern 

The  Bitterroot  Mountainshell  {Oreohelix  amariradix)  is  a  Species  of  Concern  in  Montana 
because  it  is  a  local  endemic  so  far  documented  only  in  the  Lolo  Creek  drainage ,  despite 
several  decades  of  collecting  in  the  region  by  Dr.  R.  B.  Brunson  and  students  (Frest  and 
Johannes  1 995).  Population  size  and  trends  are  unknown. 

B.  Threats 

Habitat  occupied  by  Oreohelix  amariradix  (low  elevation  talus  in  slopes  of  open  ponderosa 
pine)  is  threatened  by  logging,  grazing,  weed  control,  highway  development,  home  development, 
and  fire.  The  impact  of  fire  retardant  on  this  and  other  terrestrial  moUusks  in  not  known.  Little 
is  known  about  this  species,  including  its  susceptibility  to  disturbance. 

C.  Distribution  Relative  to  Land  Allocations 

The  known  sites  (Appendix  B)  are  on  or  near  Lolo  National  Forest  lands,  as  well  as  private 
timber  company  lands.  It  is  quite  possible  that  additional  populations  occur  on  both,  as  well  as 
other  private  lands.  None  of  the  sites  have  special  protection. 


22 


Figures.  Distribution  of   Oreohelix carinifera     in  Montana. 


•     Oreohelix  carinifera 
^^/Continental  Divide 
US  Forest  Service 


24 


SPECIES:  Oreohelix  carinifera  (Keeled Mountainsnail) 

HeritageRank:Gl,Sl 

Natural  History 

A.  Taxonomy 

Family:  Oreohelicidae 

Oreohelix  carinifera  Vilsbry,  1912 

Affinities  of  this  species  are  with  the  Oreohelix  yavapai  group  (Pilsbry  1933,  Frest  and 
Johannes  1 995),  and  based  primarily  on  the  intemal  anatomy.  Pilsbry  (1 939)  placed  all 
Oreohelix  in  the  Xanthonycidae. 

B.  Species  Description 

Morphology:  Pilsbry  (1912, 1933, 1939)  describes  the  shell  as  "lenticular,  carinate,  umbilicate, 
the  umbilicus  contained  41/3  times  in  the  diameter.  The  whorls  increase  slowly,  the  first  2  Yi 
strongly  convex,  the  rest  strongly  convex  around  the  upper  (inner)  part,  becoming  concave  near 
the  outer  (peripheral)  edge.  The  embryonic  whorls  are  very  finely  obliquely  striate;  later  whorls 
rather  coarsely  wrinkle-striate,  with  some  weak  spiral  striae  in  places;  the  last  whorl  is  concave 
above  and  below  the  peripheral  keel,  descends  very  little  or  not  at  all  in  front, . . .  The  aperture 
is  about  as  high  as  wide,  and  shows  a  slight  angle  at  the  end  of  the  keel."  Shell  diameter  9-12 
mm;  shell  height  5-7  mm;  whorls  4/^-5.  The  intemal  anatomy  is  described  in  Pilsbry  (1 933, 
1939). 

Reproductive  biology:  Hermaphroditic  (Pilsbry  1933, 1939).  There  is  no  description  of 
reproductive  behavior  and  its  seasonal  occurrence.  Life  span  is  unknown.  Age/size  at 
reproductive  maturity  is  unknown. 

Ecology:  This  species  occupies  small  limestone  outcrops  and  sandy  limestone  soils  on  arid 
slopes  with  sparse  vegetation  cover;  described  sites  have  been  south  facing  (Frest  and  Johannes 
1 995,  L.  Fairbanks  personal  communication).  Vegetation  at  sites  includes  open  stands  of 
sagebrush  (Artemisia)/}unvpQY  (Juniperus)  and  Douglas-fir  (Pseudotsuga  menziesii). 
Individuals  have  often  been  found  under  shrubs  and  junipers.  Food  habits  are  not  described. 

C.  Range  and  Known  Sites 

Oreohelix  carinifera  is  known  in  Montana  from  four  sites  in  the  Clark  Fork  River  drainage, 
Powell  and  Granite  counties  (Fig.  5,  Appendix  B)  at  1 250- 1 480  m  (4 1 00-4850  ft)  elevation. 
Frest  and  Johannes  (1 995)  found  the  species  at  a  portion  of  the  type  locality  at  Garrison,  but 
failed  to  at  another  former  location  near  Beavertail  Hill  where  the  species  was  present  in  1 975. 
There  have  been  few  or  no  additional  searches  for  this  species  at  former  sites  in  recent  years. 


25 


In  August  2002,  however,  dead  shells  were  found  at  a  new  site  in  the  Garnet  Range  (personal 
observation),  indicating  that  additional  sites  are  possible. 

Both  Pilsbry  (1 939)  and  Frest  and  Johannes  (1 995)  listed  O.  carinifera  as  endemic  to 
Montana,  but  the  species  is  on  the  Wyoming  checklist  (Beetle  1 989)  for  Park  County. 
Interestingly,  Beetle  ( 1 96 1 )  earlier  identified  this  species  from  the  Big  Horn  Mountains  in  Big 
Horn  and  Washakie  counties,  of  which  neither  location  appeared  on  her  1 989  state  checklist.  It 
is  assumed  in  the  present  report  that  Oreohelix  carinifera  is  a  local  endemic  in  Montana,  as 
stated  by  Frest  and  Johannes  (1 995);  the  Wyoming  material  needs  reexamination  by  experts  for 
final  determination,  as  there  are  other  small  Oreohelix  species  present  in  that  portion  of 
Wyoming  with  which  O.  carinifera  might  be  confused. 

D.  Species  Abundance 

Oreohelix  carinifera  is  a  local  endemic  restricted  to  the  upper  Clark  Fork  River  drainage. 
There  are  no  published  estimates  of  population  size  or  relative  abundance.  Pilsbry  (1912)  noted 
that  where  the  shells  were  "so  abundant  as  to  attract  the  attention  of  non-conchological 
naturalists"  (p.  88)  there  are  plenty  of  living  snails  to  be  found  nearby  (the  first  collection  was 
made  by  two  entomologists).  Frest  and  Johannes's  (1 995)  limited  success  at  locating  the 
species  in  the  last  decade,  including  finding  dead  shells  where  live  ones  were  absent,  suggests 
that  population  sizes  may  be  in  recent  decline,  with  possible  extinctions  at  some  sites. 

Current  Status 

A.  Why  Species  is  of  Conservation  Concern 

The  Keeled  Mountainshell  {Oreohelix  carinifera)  is  a  Species  of  Concern  in  Montana  because 
it  is  a  local  endemic  so  far  documented  only  in  the  upper  Clark  Fork  River  drainage  between 
Garrison  and  Missoula,  despite  several  decades  of  collecting  in  the  region  by  Dr.  R.  B.  Brunson 
and  his  students  (Frest  and  Johannes  1 995).  Population  size  and  trends  are  largely  unknown. 

B.  Threats 

Habitat  occupied  by  Oreohelix  carinifera  (low-elevation  slopes  of  open  juniper  and  Douglas- 
fir)  is  threatened  by  logging,  grazing,  weed  control,  highway  development,  home  development, 
and  fire.  The  impact  of  fire  retardants  on  this  and  other  terrestrial  moUusks  in  not  known.  Little 
is  known  about  this  species,  including  its  susceptibility  to  disturbance. 

C.  Distribution  Relative  to  Land  Allocations 

The  known  sites  are  on  or  near  private  timber  land,  Lolo  National  Forest  land,  state  land. 
Bureau  of  Land  Management  land,  and  private  non-timber  land.  None  of  these  sites  have 
special  protection. 


26 


Figure  6.  Distribution  of   Oreohelix  eirodi     in  Montana. 


•     Oreohelix  eirodi 
^^/Continental  Divide 
US  Forest  Service 


28 


SPECIES:  Oreohelix  elrodi  (Carinate  Mountainsnail) 

HeritageRank:Gl,Sl 

Natural  History 

A.  Taxonomy 

Family:  Oreohelicidae 
Oreohelix  elrodi  (Vilshry,  1900) 

Originally  named  Pyramidula  elrodi  by  Pilsbry  (1900).  AflFmities  of  this  species  are  with  the 
Oreohelix  strigosa  group  (Pilsbry  1933,  Frest  and  Johannes  1995),  based  on  the  internal 
anatomy  (see  Pilsbry  1939);  additional  description  of  the  intemal  anatomy  is  available  in 
Fairbanks  (1 984).  Pilsbry  (1 939)  placed  all  Oreohelix  in  the  Xanthonycidae. 

B.  Species  Description 

Morphology:  Pilsbry  (1900, 1939)  describes  the  shell  as  "strongly  depressed,  biconvex,  acutely 
carinate,  with  open  umbilicus  contained  about  4  times  in  the  diameter;  pale  vinaceous  fawn  color 
to  nearly  white  (under  a  fugacious  light  brownish  cuticle  which  is  lost  in  all  adult  shells  seen). 
Spire  low  conoidal,  often  much  depressed.  Embryonic  shell  of  2  1/3  to  2  2/3  whorls,  the  first 
smooth,  the  rest  varying  from  unevenly  striate  to  finely  costellate.  Later  whorls  are  coarsely 
sculptured  with  rude,  unequal,  retractive  ribs,  usually  narrower  than  their  intervals,  which  are 

densely  and  finely  striate  spirally The  last  whorl  descends  shortly  in  front.  Aperture  angular 

at  termination  of  the  keel."  Shell  diameter21-28  mm  (Pilsbry  1939),  17.4-26.0  mm  (Fairbanks 
1984),  4. 1-22.6  mm  (Hendricks  1998);  shell  height  8.8-13.3  mm  (Pilsbry  1939),  8.4-13.1  mm 
(Fairbanks  1984);  whorls  5-5  V2  (Pilsbry  1939),  5-5  Va  (Fairbanks  1984).  Shell  diameter  of 
new-bom  young  3.6-3.7  mm;  whorls  2.3-2.5  (Hendricks  unpubhshed  data).  The  intemal 
anatomy  is  described  in  Pilsbry  (1 939)  and  Fairbanks  (1 984). 

Reproductive  biology:  Hermaphroditic  (Pilsbry  1939,  Fairbanks  1984).  There  is  no  description 
of  reproductive  behavior  and  its  seasonal  occurrence.  Life  span  is  unknown.  Age/size  at 
reproductive  maturity  is  unknown;  a  captive  adult  1 8.2  mm  diameter  gave  birth  to  4  young  after 
overwintering  (Hendricks  unpublished  data). 

Ecology:  This  species  occupies  course  talus,  typically  on  south-facing  slopes,  and  usually  with 
sparse  canopy  of  ponderosapine  {Pinus ponderosa),  mountain  ash  (Sorbus)  and  serviceberry 
(Amelanchier)  (Frest  and  Johannes  1 995).  Hendricks  (1 998)  described  vegetation  at  three 
talus  sites  in  the  Mission  Range,  each  with  0%  canopy  cover  in  the  search  areas,  as  bordered 
by  Douglas-fir  (Pseudotsuga  menziesii)  and  ponderosa  pine  with  pockets  of  water  birch 
(Betula  occidentalis),  quaking  aspen  (Populus  tremuloides)  and  mock  orange  (Philadelphus 
lewisii).  At  the  two  Swan  Range  locations,  portions  of  the  occupied  terrain  (Hendricks 
unpublished  data)  are  in  talus  under  a  forest  canopy  variably  composed  (depending  on 


29 


microsite)  of  Douglas-fir,  ponderosapine,  quaking  aspen,  western  red  cedar  (Thuja plicata), 
paper  birch  (B.  papyrifera)  and  western  larch  (Larix  occidentalis);  canopy  cover  is  0-10%. 

Elrod  (1 902)  considered  O.  elrodi  to  be  "a  shell  of  the  rocks"  (p.  1 1 7),  present  on  the  surface 
of  exposed  talus  during  favorable  conditions,  and  present  down  among  the  stones  when 
conditions  become  dry  (Elrod  1903  a).  During  favorable  surface  conditions  (wet,  10-17°C)  live 
individuals  are  found  attached  to  rocks  near  the  surface  but  more  often  are  present  on  organic 
litter  accumulations  within  the  talus;  some  aestivating  mature  individuals  (18-21  mm  diameter) 
are  found  near  the  talus  surface  during  dry  and  warm  (2 1  -23°C)  conditions  (Hendricks  1 998). 
Food  habits  are  not  described,  but  presence  on  organic  litter  indicates  O.  elrodi  may  be  a 
detritivore. 

Occupied  talus  at  the  Mission  Range  site  is  described  by  Berry  (1 955)  and  Frest  and  Johannes 
(1 995)  as  limestone.  However,  Hendricks  (1 998)  found  O.  elrodi  in  this  mountain  range  at 
sites  comprised  mostly  of  diorite  and/or  argillite;  rock  type  at  the  two  occupied  sites  in  the  Swan 
Range  is  also  argillite  (Hendricks  unpublished  data).  Clast  (fragment)  size  of  the  rocks 
comprising  occupied  talus  ranges  from  1 0  x  20  x  1 0  cm  to  1  m^  at  the  Mission  Range  sites 
(Hendricks  1 998),  and  1 0  x  1 0  x  1 0  cm  to  0.5  x  0.5  x  0.5  m  at  the  Swan  Range  sites 
(Hendricks  unpublished  data).  Measured  slope  at  occupied  sites  in  both  mountain  ranges  was 
25-36°  (Hendricks  1 998,  unpublished  data).  How  deep  into  talus  slopes  this  species  occurs  is 
unknown,  but  live  individuals  were  found  up  to  a  meter  below  the  surface  at  the  Mission  Range 
microsite  co-occupied  by  Discus  brunsoni  (see  Hendricks  1998). 

C.  Range  and  Known  Sites 

Oreohelix  elrodi  is  endemic  to  northwestern  Montana,  known  from  three  sites  in  Lake  County: 
one  (the  type  locality)  in  the  McDonald  Lake  cirque  on  the  west  side  of  the  Mission  Range  at 
1 067-1 524  m  (3500-5000  ft)  elevation  (Elrod  1 902  states  shells  occur  up  to  2286  m  or  7500 
ft  elevation),  two  on  the  west  side  of  the  Swan  Range  at  1 1 58-1295  m  (3800-4250  ft)  elevation 
along  Lion  and  Goat  creeks  (Fig.  6,  Appendix  B).  Live  animals  were  found  at  the  type  locality 
in  the  Mission  Range  as  recently  as  1 997  (Hendricks  1 998),  and  in  1 999  at  both  the  Lion 
Creek  site  and  the  Goat  Creek  site  (which  was  discovered  in  1 999).  There  have  been  few  or 
no  additional  searches  for  this  species  at  the  above  sites,  and  no  additional  surveys  for  new 
localities  in  either  mountain  range. 

D.  Species  Abundance 

Oreohelix  elrodi  is  a  local  endemic  restricted  to  the  Mission  and  Swan  ranges.  There  are  no 
published  estimates  of  population  size.  Elrod  (1901-1902, 1902, 1903  a)  stated  dead  shells 
were  abundant  in  many  locations  on  the  slopes  above  McDonald  Lake  but  live  animals  were 
relatively  uncommon  sometimes.  Live  O.  elrodi  were  4-6  times  more  abundant  than  Discus 
brunsoni  near  the  talus  surface  in  the  microsite  where  the  two  species  are  sympatric.  Among 
the  three  sites,  live  individuals  were  found  at  a  rate  of  0. 1 67/min  on  1  July  at  the  type  locality 
co-occupied  by  D.  brunsoni,  0. 1 74/min  on  1 9  May  at  Lion  Creek,  and  0.350/min  on  9  June  at 
Goat  Creek;  conditions  were  overcast,  wet  and  7-1 FC  at  the  time  of  the  searches  (Hendricks 


30 


1 998,  unpublished  data).  Population  trends  are  unknown,  but  the  species  has  persisted  at  the 
type  locality  for  a  century  following  its  discovery  in  1 899  (Elrod  1 903a). 

Current  Status 

A.  Why  Species  is  of  Conservation  Concern 

The  Carinate  Mountainshell  (Oreohelix  elrodi)  is  a  Species  of  Concern  in  Montana  because  it 
is  a  local  endemic  so  far  documented  at  only  three  sites  in  the  Mission  and  Swan  ranges  of  Lake 
County,  despite  several  decades  of  collecting  in  the  region  by  Drs.  M.  J.  Elrod  and  R.  B. 
Brunson  and  their  students  (Frest  and  Johannes  1 995).  Population  size  and  trends  are 
unknown. 

B.  Threats 

Habitat  occupied  by  Oreohelix  elrodi  (low-elevation  slopes  of  mixed  conifers,  especially 
Douglas-fir,  ponderosa  pine  and  western  larch)  is  threatened  to  some  extent  by  logging,  grazing, 
and  fire,  although  occupied  habitat  is  often  in  talus  surrounded  by  mixed  coniferous  forest. 
Habitat  requirements  and  food  habits  are  poorly  understood,  however.  Fire  suppression  efforts 
(especially  use  of  fire  retardants)  and  talus  destabilization  (trail  maintenance,  modification)  could 
have  negative  impacts,  as  could  chemical  control  of  weeds. 

C.  Distribution  Relative  to  Land  Allocations 

The  type  (and  only)  locality  in  the  Mission  Range  is  in  the  Confederated  Salish  and  Kootenai 
Tribes  Mission  Mountains  Tribal  Wilderness.  A  major  hiking  and  packing  trail  bisects  the  site. 
The  Lion  Creek  site  in  the  Swan  Range  occupies  lands  administered  by  Plum  Creek  Timber 
Company  and  the  Swan  Lake  Ranger  District  of  the  Flathead  National  Forest;  a  major  hiking 
trail  bisects  the  site.  The  Goat  Creek  site  in  the  Swan  Range  occupies  lands  administered  by 
the  Swan  Lake  Ranger  District  of  the  Flathead  National  Forest.  It  is  a  small  talus  patch  just 
upslope  from  FS  Road  9530  in  an  area  where  logging  has  occurred  previously. 


31 


Figure  7.  Distribution  of   Oreohelix  strigosa  berryi     in  Montana. 


•    Oreohelix  strigosa  berryi 
^^/Continental  Divide 
US  Forest  Service 


32 


SPECIES:  Oreohelix  strigosa  berryi  (Berry's  Mountainsnail) 

Heritage  Rank:  G5T2,  S1S2 
Natural  History 

A.  Taxonomy 

Family:  Oreohelicidae 

Oreohelix  strigosa  berryi  (Pilsbry,  1915) 

Originally  described  as  a  subspecies  oi  Oreohelix  cooper i  but  changed  in  1 933  to  a  subspecies 
of  O.  strigosa  (Pilsbry  1933,  Henderson  1936),  with  cooper i  also  reduced  to  a  subspecies  of 
O.  strigosa.  External  and  internal  anatomy  indicates  O.  strigosa  berryi  is  distinct  to  the 
subspecies  level  (Pilsbry  1933, 1939,  Frest  and  Johannes  1993).  Beetle  (1989)  considered 
this  subspecies  a  form  of  O.  pygmaea,  but  Frest  and  Johannes  ( 1 993)  separate  the  forms  in  the 
Black  Hills  on  the  basis  of  shell  morphology.  Pilsbry  (1 939)  placed  all  Oreohelix  in  the 
Xanthonycidae. 

B.  Species  Description 

Morphology:  Pilsbry  (1939)  describes  the  shell  as  having  "  the  same  shape  characteristic  of  O. 
cooperi  except  that  the  last  whorl  is  distinctly  angular  in  front,  the  angle  disappearing  on  the  last 
half  or  third,  leaving  the  periphery  rounded.  Color  cinnamon  to  snuff  brown,  from  third  whorl 
profusely  marked  with  white  patches  and  narrow  streaks;  last  whorl  having  a  chocolate  band 
below  the  periphery . . .  The  surface  is  irregularly  striate  and  shows  traces  of  spiral  striation  in 
places.  Whorls  41/3,  all  convex.  Embryonic  shell  of  nearly  two  whorls,  which  are  finely  striate 
and  covered  with  very  fine  spirals,  the  last  half  of  the  second  whorl  having  distinct  spiral  striae. 
Umbilicus  narrow,  contained  5  Yi  times  in  the  diameter  of  the  shell"  (p.  445-446).  Frest  and 
Johannes  (1 993)  add  "full  adult  with  about  5-5  1/4  whorls;  shell  low  dome-shaped . . ."  (p.  76). 
Shell  diameter  7-13  mm  (types  9.3  and  9.4  mm);  shell  height  of  types  6. 1  and  6.3  mm  (Pilsbry 
1939).  Intemalanatomy  described  in  Pilsbry  (1933, 1939). 

Reproductive  biology:  Hermaphroditic  (Pilsbry  1933, 1939).  There  is  no  description  of 
reproductive  behavior  and  its  seasonal  occurrence.  Life  span  is  unknown.  Age/size  at 
reproductive  maturity  is  unknown. 

Ecology:  Found  among  small  loose  rock,  shrubbery,  and  under  creeping  juniper  (Juniperus 
horizontalis)  on  west-facing  canyon  slopes  at  the  type  locality  in  the  Big  Snowy  Mountains, 
and  under  sticks  and  logs  in  moister  locations  in  the  same  mountain  range  (Berry  1916).  This 
snail  was  present  in  the  Mammoth  area  of  Yellowstone  National  Park  on  a  north  exposure  of 
limey  soil  with  plenty  of  cover,  but  neither  very  wet  nor  dry  (Henderson  1 936).  Substrate 
typically  is  derived  from  limestone  (Frest  and  Johannes  1 993, 1 995).  In  the  Black  Hills  and 
Bear  Lodge  Mountains  of  Wyoming  and  South  Dakota,  it  occurs  in  mixed  and  open  ponderosa 
pine  {Pinus ponderosa)  forests  with  relatively  thin  litter,  often  with  aspen  (Populus 


33 


tremuloides)  and  birch  (Betula)  in  the  canopy,  and  violets  (Viola)  and  Canada  dogwood 
(Cornus  canadensis)  in  the  understory  (Frest  and  Johannes  1 993);  the  deciduous  tree 
component  was  relatively  important  for  the  occurrence  of  this  subspecies. 

C.  Range  and  Known  Sites 

Oreohelix  strigosa  berryi  is  documented  from  several  locations  in  and  near  the  Big  Snowy 
Mountains  of  Fergus  and  Golden  Valley  counties,  Montana  (Fig.  7,  Appendix  B),  and  more 
recently  (Hendricks  unpublished  data)  from  the  Judith  Mountains,  also  in  Fergus  County,  and 
the  vicinity  of  Montanopolis  in  the  Absaroka  Mountains,  Park  County  (Frest  and  Johannes 
1995);  elevation  ranges  from  1295-2438  m  (4250-8000  ft).  Also  documented  in  Wyoming  in 
Yellowstone  National  Park  near  Mammoth  (Henderson  1933,1936,  Pilsbry  1 93  9)  and  in  the 
Black  Hills  National  Forest  of  Wyoming  and  South  Dakota  (Frest  and  Johannes  1 993). 

D.  Species  Abundance 

Oreohelix  strigosa  berryi  in  Montana  has  been  fully  documented  only  in  the  Big  Snowy 
Mountains.  Population  sizes  are  not  reported  for  any  of  the  Montana  locations,  nor  have  most 
of  these  sites  been  revisited  in  recent  decades.  Berry  (1916)  found  it  to  be  the  most 
conspicuous  land  snail  near  the  mouth  of  Swimming  Woman  Creek  Canyon  in  the  Big  Snowy 
Mountains.  Colonies  outside  of  the  Big  Snowy  Mountains  generally  appear  to  be  small  and 
isolated  (Frest  and  Johannes  1 993),  although  the  recent  collection  of  shells  in  the  Judith 
Mountains  (Hendricks  unpublished  data)  indicate  colonies,  some  fairly  large,  may  be  present  in 
some  of  the  other  "island  mountains  ranges"  of  eastern  Montana.  Henderson  (1 936)  said  the 
species  occurred  in  abundance  near  Mammoth  in  Yellowstone  National  Park,  Wyoming. 
Population  trends  are  unknown  for  any  locality. 

Current  Status 

A.  Why  Species  is  of  Conservation  Concern 

Berry's  Mountainshell  {Oreohelix  strigosa  berryi)  is  a  Species  of  Concern  in  Montana  because 
it  is  a  relict  subspecies  so  far  documented  in  Montana  at  ten  localities  in  three  mountain  ranges, 
and  only  present  in  two  additional  areas  outside  of  Montana  in  Wyoming  and  South  Dakota 
(Yellowstone  National  Park,  Black  Hills  National  Forest)  despite  several  decades  of  collecting 
in  the  region  by  Dr.  R.  B.  Brunson  and  Stillman  Berry.  Population  size  and  trends  in  Montana 
are  unknown,  but  outside  of  Montana  where  intensive  surveys  have  been  undertaken  in  recent 
years  (Frest  and  Johannes  1 993)  this  subspecies  appears  to  exist  in  only  a  few  small  colonies. 

B.  Threats 

Habitats  occupied  by  Oreohelix  strigosa  berryi  are  may  be  threatened  by  logging  and  grazing, 
and  possibly  weed  control  and  mining,  but  most  documented  localities  have  not  been  revisited  in 
decades,  so  current  threats  are  unknown.  Fire  and  fire  suppression  efforts  could  have  negative 
impacts  (numerous  dead  shells  found  in  the  Judith  Mountains  were  in  a  decade-old  bum). 


34 


Logging  and  grazing  threaten  the  Black  Hills  National  Forest  colonies  (Frest  and  Johannes 
1 993).  Habitat  requirements  and  food  habits  are  poorly  understood.  Colonies  may  be  local 
and  small. 

C.  Distribution  Relative  to  Land  Allocations 

The  type  locality  (Swimming  Woman  Creek  Canyon)  and  all  other  known  locations  (six  total)  in 
the  Big  Snowy  Mountains  are  on  lands  administered  by  the  Musselshell  Ranger  District  of  the 
Lewis  and  Clark  National  Forest.  Two  other  sites  north  of  the  Big  Snowy  Mountains 
apparently  are  on  private  and  possibly  state  land.  The  site  in  the  Judith  Mountains  is  on  land 
administered  by  the  Lewistown  Field  Office  of  the  Bureau  of  Land  Management.  The  Park 
County  site  is  on  land  administered  by  the  Livingston  Ranger  District  of  the  Gallatin  National 
Forest. 


35 


Figures.  Distribution  of   Oreohelix yavapai mariae    in  Montana. 


•  Oreohelix  yavapai  maria^ 
^^/Continental  Divide 
US  Forest  Service 


36 


SPECIES:  Oreohelix yavapai  mariae  (Gallatin Mountainsnail) 

HeritageRank:G4?Tl,Sl 

Natural  History 

A.  Taxonomy 

Family:  Oreohelicidae 

Oreohelix  yavapai  mariae  Bartsch,  1916 

The  original  description  of  this  taxon  by  Bartsch  (1916)  and  his  placement  as  a  subspecies  of 
Oreohelix  yavapai  are  still  valid.  Pilsbry  (1 939)  and  Frest  and  Johannes  (1 995)  consider  this 
taxon  distinct  from  another  subspecies,  O.  yavapai  extremitatis,  that  is  present  in  the  Big  Horn 
Mountains,  Wyoming,  and  the  nearby  Bridger  Range,  Montana.  Pilsbry  (1 939)  placed  all 
Oreohelix  in  the  Xanthonycidae. 

B.  Species  Description 

Morphology:  Bartsch  (1916)  describes  the  shell  as  "decidedly  depressed  helicoid,  almost 
lenticular,  flesh  colored,  with  a  narrow  brown  band  on  the  upper  surface,  which  is  a  little  nearer 
the  peripheral  cord  than  the  suture,  and  a  second  even  narrower  one  bordering  the  peripheral 
cord  on  the  lower  surface.  Nuclear  whorls  scarcely  differentiated  from  succeeding  turns, 
bearing  the  same  sculpture  as  the  adult  whorls,  but  a  little  less  strongly  expressed.  Periphery  of 
the  whorls  provided  with  a  cord-like  keel,  which  becomes  somewhat  weakened  on  the  last 
quarter  of  the  last  turn.  Entire  surface  both  above  and  below  marked  by  slender  thread-like 
incremental  lines  and  fine  spiral  striations;  last  whorl  slightly  descending  near  the  aperture.  Base 
broadly,  openly  umbilicated,  well  rounded;  a  little  more  convex  at  the  umbilical  wall  than  at  the 
lateral  margin.  Aperture  very  oblique,  oval;  peristome  neither  thickened  nor  refiected  at  the 
edge;  parietal  wall  strong,  rendering  the  peristome  complete"  (p.  331).  Shell  diameter  20.7  mm 
(1 8.3-22.5  mm;  n  =  9);  shell  height  9.2  mm  (8.2-1 0.0  mm;  n  =  9);  number  of  whorls  5.5  (5.2- 
5.6;  n  =  9).  Internal  anatomy  not  described. 

Reproductive  biology:  Presumably  hermaphroditic,  but  the  intemal  anatomy  is  not  described. 
There  is  no  description  of  reproductive  behavior  and  its  seasonal  occurrence.  Life  span  is 
unknown.  Age/size  at  reproductive  maturity  is  unknown. 

Ecology:  Present  on  a  south-facing  slope  in  grassy  habitat  near  the  base  of  a  limestone  outcrop 
(L.  Fairbanks  personal  communication).  Nothing  else  about  the  ecology  of  this  species  is 
known  or  described. 

C.  Range  and  Known  Sites 

Known  only  from  the  type  locality  at  Squaw  Creek  near  the  mouth  of  Gallatin  Canyon  in  the 
Gallatin  Range,  Gallatin  County,  Montana  (presumably  above  the  confiuence  of  Squaw  Creek 


37 


with  the  Gallatin  River)  at  1 707  m  (5600  ft)  elevation  (Fig.  8,  Appendix  B). 

D.  Species  Abundance 

No  inft)nnation.  Specimens  have  been  collected  at  the  type  locality  as  recently  as  1 976  (L. 
Fairbanks  personal  communication).  Population  trends  are  unknown. 

Current  Status 

A.  Why  Species  is  of  Conservation  Concern 

The  Gallatin  Mountainshell  (Oreohelix  yavapai  mariae)  is  a  Species  of  Concern  in  Montana 
because  it  is  known  only  fi-om  a  single  locality.  Decades  of  collecting  across  Montana  by  R.  B. 
Brunson,  Stillman  Berry,  and  others  have  revealed  no  additional  colonies,  although  additional 
searches  in  the  Gallatin  Range  may  result  in  discovery  of  additional  populations. 

B.  Threats 

Logging  and  road  construction  along  the  Gallatin  River  and  Squaw  Creek  are  likely  the  main 
threats  that  could  impact  the  only  known  population  (Frest  and  Johannes  1 995).  Fire,  fire 
suppression,  weed  control,  and  grazing  could  also  have  negative  impacts. 

C.  Distribution  Relative  to  Land  Allocations 

The  only  known  site  is  on  lands  administered  by  the  Bozeman  Ranger  District  of  the  Gallatin 
National  Forest. 


38 


Figure  9.  Distribution  of   Hemphillia  danieisi  in  Montana. 


•     Hemphillia  danieisi 
^^/Continental  Divide 
US  Forest  Service 


40 


SLUGS 
SPECIES:  Hemphillia  danielsi  (Marbled  Jumping-slug) 

Heritage  Rank:  G1G3,  S1S3 
Natural  History 

A.  Taxonomy 

Family:  Arionidae 

Hemphillia  danielsi  Vanatta,  1914 

The  original  species  description  by  Vanatta  ( 1 9 1 4,  see  also  Pilsbry  1 948)  and  placement  in  the 
Arionidae  are  still  valid.  This  species  is  the  eastern-most  member  of  a  small  genus  restricted  to 
the  Pacific  Northwest. 

B.  Species  Description 

Morphology:  Vanatta  {\9\AJn  Pilsbry  1948)  describes  Hemphillia  danielsi  as  "sluglike,  with 
the  shell  partly  exposed,  and  the  mantle  elevated  into  a  visceral  hump,  as  usual  in  this  genus. 
The  color  in  formalin  is  yellowish-gray  with  bluish-black  markings,  but  in  alcohol  it  is  white  with 
black  maculations.  The  shell  pore  is  about  one-third  the  length  of  the  mantle.  The  posterior 
part  of  the  foot  is  narrow,  with  a  dorsal  median  groove  and  a  tail  pore"  (p.  747).  Length  3 .4  cm 
(Vanatta  1914,  Pilsbry  1948);  Pilsbry  considered  this  individual  an  immature.  A  recent 
specimen  collected  along  Mill  Creek  (Appendix  B)  measured  6.4  cm  (Hendricks  unpublished 
data),  and  Pilsbry  (1948)  quotes  L.E.  Daniels  as  stating  that  the  living  slug  is  "about  two  inches 
[5.1  cm]  long,  with  a  high  hump  showing  the  shell"  (p.  748).  In  live  animals,  and  some 
preserved  specimens,  the  tail  portion  of  the  foot  is  laterally  compressed,  keeled,  and  tipped  with 
a  horn-like  projection  (Hendricks  personal  observation;  see  also  photos  oiH  dromedarius  in 
Ovaska  et  al.  2002).  Internal  anatomy  is  described  in  Vanatta  (1914)  and  Pilsbry  (1948). 

Reproductive  biology:  Hermaphroditic,  based  on  internal  anatomy;  the  congeneric  Malone 
Jumping-slug  {Hemphillia  malonei)  is  hermaphroditic,  but  spermatophore  delivery  is 
sometimes  non-reciprocal  (Leonard  and  Ovaska  2002).  There  is  no  description  of  the 
reproductive  behavior  and  biology  of /Z  danielsi,  but  it  may  be  similar  to  H  malonei  for  which 
there  exists  a  recent  description  of  breeding  behavior  in  captivity  (Leonard  and  Ovaska  2002). 
H  malonei  captive-raised  from  eggs  reached  sexual  maturity  in  the  first  year. 

Ecology:  There  are  few  descriptions  of  the  habitat  occupied  by  this  species.  Frest  and  Johannes 
(1 995)  indicate  that  moderate-elevation  ponderosa  pine  forest  (Pinus ponderosa)  is 
characteristic;  moist  valley,  ravine,  gorge,  or  talus  sites  are  preferred  (i.e.,  low  on  slopes  near 
water).  This  description  is  supported  by  more  recent  observations  (W.  Leonard,  B.  Maxell,  H. 
Reise  personal  communications).  Each  of  the  correspondents  reported  finding  Hemphillia 
danielsi  in  riparian  areas  very  near  water  (Appendix  B).  Sites  included  an  overstory  of 


41 


deciduous  and  coniferous  trees  and  shrubs  (Picea  engelmanii,  Pseudotsuga  douglasii, 
Populus,  Alnus).  Rock  or  soils  at  known  sites  have  not  been  described,  but  igneous  rock 
types  dominate  the  range  of  this  species. 

C.  Range  and  Known  Sites 

Hemphillia  danielsi  is  virtually  a  Montana  endemic  known  only  from  the  eastern  side  of  the 
Bitterroot  Mountains  in  Ravalli  County  (Fig.  9,  Appendix  B),  with  the  exception  of  one  or  two 
records  a  short  distance  west  of  the  Bitterroot  crest  into  Idaho  (see  below);  the  type  locality  is 
at  Camas  Creek.  Five  total  sites  in  Montana  have  been  documented,  from  Mill  Creek  in  the 
north  to  Medicine  Hot  Springs  in  the  south  at  elevations  between  1341-1 524  m  (4400-5000 
ft).  Two  of  the  five  sites  (Bunkhouse  Creek,  Mill  Creek)  were  first  discovered  in  2001 . 
Additional  populations  in  the  Bitterroot  Mountains  are  likely  to  be  discovered  as  more  surveys 
are  conducted.  Hemphillia  danielsi  has  been  documented  infrequently  in  surveys  on  the  Idaho 
side  of  the  Bitterroots  (Frest  and  Johannes  1 995);  the  first  Idaho  record  apparently  is  that  of 
Webb  (1959)  near  Lolo  Pass,  and  Hemphillia  collected  more  recently  at  the  confiuence  of 
Apgar  Creek  with  the  Lochsa  River  in  Idaho  County  may  be  this  species  (W.  Leonard  personal 
communication). 

D.  Species  Abundance 

No  information.  Animals  were  collected  at  the  type  locality  as  recently  as  2001  (H.  Reise 
personal  communication),  four  individuals  were  found  at  the  Bunkhouse  Creek  site  in  200 1 ,  two 
individuals  at  the  Mill  Creek  site  in  2001  (W.  Leonard,  B.  Maxell  personal  communications). 


Current  Status 


A.  Why  Species  is  of  Conservation  Concern 

The  Marbled  Jumping-slug  {Hemphillia  danielsi)  is  a  Species  of  Concern  in  Montana  because 
it  is  nearly  a  Montana  endemic  so  far  documented  at  but  five  sites  in  the  Bitterroot  Mountains  of 
Ravalli  County,  despite  several  decades  of  collecting  in  the  region  by  Dr.  R.  B.  Brunson  and 
students  (Frest  and  Johannes  1 995).  Population  sizes  and  trends  are  unknown. 

B.  Threats 

Habitat  occupied  by  Hemphillia  danielsi  (moderate  elevation  mixed  conifer  forest,  often  near 
water)  is  threatened  by  logging,  grazing,  fire,  and  possibly  weed  control  and  rural  home 
development.  The  impact  of  fire  retardant  on  this  and  other  terrestrial  moUusks  is  not  known. 
Little  is  known  about  this  species,  including  its  sensitivity  to  disturbance. 


42 


C.  Distribution  Relative  to  Land  Allocations 

Probably  four,  and  possibly  all,  of  the  known  sites  in  Montana  (Appendix  B)  are  on  lands 
administered  by  the  Stevensville,  Darby,  and  Sula  Ranger  Districts  of  the  Bitterroot  National 
Forest.  The  specific  collection  site  at  Medicine  Hot  Springs  is  uncertain  and  may  be  on  private 
land. 


43 


Figure  10.  Distribution  of  Magnipelta  mycophaga     in  Montana. 


•     Magnipelta  mycophaga 
^^/Continental  Divide 
US  Forest  Service 


44 


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^^^^^^^^HRr        l^F^ 

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F-_  ^^j  fc  'L_Ji^3Liia  l^^^^^^^^B 

'•'       '^\^^^^| 

'■jAmW^^HH 

SPECIES:  Magnipelta  mycophaga  (Spotted  Slug) 

Heritage  Rank:  G2G3,  S1S3 
Natural  History 

A.  Taxonomy 

Family:  Arionidae 

Magnipelta  mycophaga  Pilsbry,  1 953 

The  original  species  description  by  Pilsbry  (1 953,  see  also  Pilsbry  and  Brunson  1 954)  and 
placement  in  the  Arionidae  are  still  valid,  although  Webb  and  Russell  ( 1 977)  noted  possible 
alliance  with  the  Camaenidae,  based  on  anatomical  features.  The  genus  is  monospecific  and 
restricted  to  the  interior  Pacific  Northwest. 

B.  Species  Description 

Morphology:  Does  not  closely  resemble  any  other  described  North  American  slug  (Frest  and 
Johannes  1 995).  In  the  original  description,  based  on  an  immature  specimen,  Pilsbry  (1 953) 
states  the  appearance  of  Magnipelta  mycophaga  as  "characterized  by  the  structure  of  the 
mantle  and  foot ...  the  mantle  covering  far  the  greater  part  of  the  upper  surface.  The  mantle  is 
free  anteriorly  for  more  than  one-fourth  of  its  length,  smooth,  chamois  colored  with  an  irregular 
black  stripe  on  each  side  and  elsewhere  unevenly  spotted  with  black.  The  quite  short 
respiratory  slit  is  slightly  post-median  on  the  right  side.  Length  of  mantle  1 6  mm.  The  foot  is 
lighter  colored  than  the  mantle,  spotted  with  black  on  the  flanks  posteriorly.  It  has  an  irregular 
polygonal  impressed  reticulation.  The  pedal  margin  is  quite  narrow,  the  pedal  grooves  meeting 
above  the  tail  without  any  trace  of  a  caudal  pore.  The  sole  is  transversely  wrinkled  at  the  sides, 
the  middle  third  smoother,  but  it  is  not  distinctly  tripartite"  (p.37-38).  In  a  second  preserved 
and  partly  contracted  specimen  collected  at  a  later  date  the  mantle  measured  34  mm  in  length, 
free  anteriorly  for  9  mm  and  posteriorly  for  5  mm  (Pilsbry  and  Brunson  1 954);  in  this  specimen 
the  slit  to  the  pneumostome  was  1 5  mm  from  the  anterior  end  of  the  mantle.  Magnipelta 
mycophaga  can  be  a  moderately  large  slug;  a  May  sample  of  12  extended  animals  ranged  from 
1 .5-6.7  cm  (mean  =  3.6  cm),  a  June  sample  of  20  animals  from  the  same  locality  ranged  from 
1 .4-8.0  cm  (mean  =  4.3  cm)  (Brunson  and  Kevem  1 963).  Two  other  individuals  from  widely 
separate  localities  measured  ca.  7.0  cm  and  8.0  cm  (Hendricks  personal  observation).  Internal 
anatomy  is  described  and  illustrated  in  Pilsbry  (1 953),  Pilsbry  and  Brunson  (1 954),  and  Webb 
and  Russell  (1977). 

Reproductive  biology:  Hermaphroditic,  based  on  internal  anatomy  (Pilsbry  and  Brunson  1 954, 
Webb  and  Russell  1 977).  There  is  no  description  of  reproductive  behavior  and  its  seasonal 
occurrence;  Pilsbry  and  Brunson  (1 954)  suggest  reproduction  may  occur  early  in  the  year, 
based  on  finding  immature  animals  in  late  May.  Life  span  is  unknown.  Age/size  at  reproductive 
maturity  is  unknown,  but  Pilsbry  (1 953)  mentioned  that  the  type  specimen,  with  a  mantle  length 


45 


of  1 6  mm,  was  immature  with  a  genital  system  only  partly  developed,  the  ducts  thread-like  and 
extremely  fragile. 

Ecology:  Found  in  a  variety  of  low-  to  mid-elevation  sites,  often  with  water  in  the  general 
vicinity.  Moist,  cool  sites  in  relatively  undisturbed  forest  with  an  intact  duff  layer,  such  as  are 
found  in  moist  valleys,  ravines,  and  talus  areas,  are  preferred  (Frest  and  Johannes  1 995). 
Forest  canopy  composition  at  sites  includes  Picea  engelmannii,  Pseudotsuga  menziesU, 
Pinus ponderosa,  Pinus  albicaulis,  Larix  occidentalism  Abies  lasiocarpa,  dind  Abies 
grandis,  often  with  Alnus  present  (Appendix  B;  Pilsbry  and  Brunson  1 954,  Brunson  and 
Kevem  1 963,  Hendricks  personal  observation);  spruce-fir  appears  to  be  the  most  frequent 
forest  association.  The  Thompson  River,  Sanders  County  location  (Appendix  B)  is  an  area  of 
near-minimal  tree  canopy  cover,  though  brushy,  indicating  slugs  may  move  some  distance  when 
conditions  are  favorable,  or  that  the  species  can  persist  in  some  relatively  exposed  and 
disturbed  habitats.  Often  found  on  the  ground  under  pieces  of  loose  bark,  logs,  loose  stones, 
and  in  rotted  wood;  surface  active  on  cool  (10-1 6°C),  wet  and  overcast  days,  probably  most 
active  at  night.  Feeds  on  green  plant  material,  possibly  including  moss  (Brunson  and  Kevem 
1 963);  the  type  specimen  was  found  feeding  on  one  of  the  larger  fungi,  hence  the  specific  Latin 
name  of  the  species  (Pilsbry  1953). 

C.  Range  and  Known  Sites 

Magnipelta  mycophaga  is  found  in  northwestern  Montana,  northern  Idaho,  northeastern 
Washington  (Frest  and  Johannes  1 995),  and  probably  adjacent  regions  of  British  Columbia.  In 
Montana,  this  species  has  been  documented  at  six  localities  in  four  counties:  Flathead,  Lincoln, 
Missoula,  and  Sanders  (Fig.  1 0,  Appendix  B).  Aprobable  seventh  Montana  locality,  mentioned 
in  Pilsbry  and  Brunson  (1 954)  as  in  the  Blackfoot  Valley  near  Bonner,  Missoula  County,  was 
too  vague  to  be  mapped  and  was  not  included  in  Appendix  B;  the  Lincoln  County  site,  centered 
on  McGuire  Creek  in  the  Ural-Tweed  Bighorn  Sheep  range  (see  Forrester  1 960, 1 962)  is  also 
poorly  described  in  the  literature,  but  included  in  Appendix  B  because  it  represents  a  location 
far  removed  from  other  reported  sites.  This  slug  species  has  been  found  at  elevations  between 
762-  1585m  (2500-5200  ft)  in  Montana,  and  up  to  ca.  1 829  m  (6000  ft)  in  northeastern 
Washington  (T.  Burke  personal  communication).  The  Deer  Creek,  Missoula  County,  colony 
site  is  described  by  Brunson  and  Kevem  (1 963)  as  about  400  m  (440  yds)  in  length.  Additional 
populations  in  northwestern  Montana  are  likely  to  be  discovered  with  additional  survey  effort, 
given  that  half  of  the  known  Montana  sites  were  found  since  1 998. 

D.  Species  Abundance 

Almost  no  information.  In  1 954  at  the  Deer  Creek,  Missoula  County  site  1 9  individuals  were 
found  in  May  and  1 0  in  June.  Counts  at  the  same  locality  in  1 957  were  29  April:  1 , 5  May:  1 , 
10  May:  12, 1  June:  18, 7  June:  86, 23  June:  20, 20  July:  4, 4  August:  3, 5  September:  10, 22 
September:  1  (Brunson  and  Kevem  1 963),  indicating  that  the  species  may  be  relatively 
abundant  in  some  localities.  Numbers  reported  at  other  sites  are  1  -2  individuals,  but  none  of 
these  sites  have  been  visited  more  than  twice,  nor  searched  thoroughly  like  the  Deer  Creek  site. 


46 


Apparently  the  Deer  Creek  site  has  not  been  revisited  in  recent  decades,  but  the  species 
persists  (as  of  2001)  at  the  Little  Park  Creek  site  only  5.6  km  (3.5  mi)  to  the  south. 

Current  Status 

A.  Why  Species  is  of  Conservation  Concern 

The  Spotted  Slug  {Magnipelta  mycophaga)  is  a  Species  of  Concern  in  Montana  because  it  is 
a  regional  endemic  so  far  documented  at  six  sites  in  four  Montana  counties,  despite  several 
decades  of  collecting  in  the  region  by  Dr.  R.  B.  Brunson  and  his  students  (Frest  and  Johannes 
1 995),  and  limited  collecting  by  others  in  recent  years.  Population  sizes  and  trends  are 
imknown. 

B.  Threats 

Habitat  occupied  by  Magnipelta  mycophaga  (moderate  elevation  mixed  conifer  forest, 
especially  spruce-fir,  often  near  water)  is  threatened  by  logging,  grazing,  fire,  possibly  rural 
home  development,  and  possibly  recreation  and  weed  control.  The  impact  of  fire  retardant  on 
this  and  other  terrestrial  moUusks  is  not  known.  Little  is  known  about  this  species,  including 
sensitivity  to  disturbance. 

C.  Distribution  Relative  to  Land  Allocations 

Documented  Montana  sites  are  on  lands  administered  by  the  Cabinet  Ranger  District,  Kootenai 
National  Forest  (1  site),  Rexford  Ranger  District,  Kootenai  National  Forest  (1  site).  Glacier 
View  Ranger  District,  Flathead  National  Forest  ( 1  site),  Missoula  Ranger  District,  Lolo  National 
Forest  (1  site).  Plum  Creek  Timber  Company  (2  sites). 


47 


Figure  11.  Distribution  of  Zacoleus  idahoensis  in  Montana. 


•     Zacoleus  idahoensis 
^^/Continental  Divide 
US  Forest  Service 


48 


SPECIES:  Zacoleus  idahoensis  (Sheathed  Slug) 

Heritage  Rank:  G3G4,  S2S3 
Natural  History 

A.  Taxonomy 

Family:  Arionidae 

Zacoleus  idahoensis  Pilsbry,  1903 

The  original  species  descriptions  by  Pilsbry  (1 903, 1 948)  and  placement  in  the  Arionidae  are 
still  valid.  The  genus  is  monospecific  and  restricted  to  the  interior  Pacific  Northwest. 

B.  Species  Description 

Morphology:  Pilsbry  (1 948)  states  "In  the  field  this  inconspicuous  slug  might  be  mistaken  for 
Deroceras,  having  a  tripartite  sole  and  postmedian  pneumostome . . . ,  but  it  differs  by  the 
weakly  carinate  back"  (p.  732).  The  species  is  black  to  dark  brown  (deep  grayish  olive)  on  the 
mantle  and  back;  the  sole  is  cream- white.  The  reticulation  on  the  posterior  half  of  the  body 
(tail)  is  indistinct,  predominately  with  longitudinal  lines  above  and  oblique  on  the  sides.  The 
back  of  the  mantle  is  keeled,  the  tail  strongly  so.  The  oval  mantle  somewhat  exceeds  about 
one-third  the  length  of  the  body;  the  pneumostome  is  present  in  the  posterior  half  of  the  mantle 
margin.  The  foot-margin  is  rather  narrow.  There  is  no  caudal  pore,  but  the  tail  appears 
somewhat  abruptly  truncate  in  profile.  The  shell  is  completely  buried  in  the  mantle.  Body 
lengths  of  two  animals  from  Idaho  were  1 .4  cm  (mantle  length  5.5  mm)  and  2.3  cm  (Pilsbry 
1 948).  Internal  anatomy  is  described  and  illustrated  in  Pilsbry  (1 948). 

Reproductive  biology:  Hermaphroditic,  based  on  internal  anatomy  (Pilsbry  1 948).  There  is  no 
description  of  reproductive  behavior  and  its  seasonal  occurrence.  Life  span  is  unknown.  Age/ 
size  at  reproductive  maturity  is  unknown. 

Ecology:  Habitat  descriptions  are  limited.  Most  occurrences  in  Idaho  are  in  moist  microsites  in 
relatively  intact  Pseudotsuga  menziesii,  Pinus ponderosa,  and  Picea  engelmannii  forests 
(Frest  and  Johannes  1 995)  in  moist  valleys,  ravines,  and  talus  on  both  north-  and  south-facing 
slopes.  Pilsbry  (1 948)  lists  collections  made  in  meadows  and  cedar  swamps,  white  pine  stands, 
spruce  valleys,  rockslides,  and  near  springs.  Populus  and  Alnus  present  at  several  north  Idaho 
locations  (H.  Reise  personal  communication).  Rocky  substrates  include  sedimentary,  igneous 
and  metamorphic  types;  the  Prospect  Creek,  Sanders  County,  Montana  site  (Appendix  B)  is 
described  as  composed  of  calcareous  shales  (Pilsbry  1 948).  Herbivorous;  food  includes  the 
epiphytic  cryptogam  Frullania  (Pilsbry  1948). 


49 


C.  Range  and  Known  Sites 

Zacoleus  idahoensis  has  so  far  been  documented  only  in  northern  Idaho  and  northwestern 
Montana.  In  Montana,  records  exist  for  four  widely  separated  sites  in  four  counties:  Granite, 
Lake,  Lincoln,  and  Sanders  (Fig.  1 1 ,  Appendix  B).  Three  of  the  localities  (Kootenai  Falls,  Wild 
Horse  Island,  Squaw  Rock  Campground)  were  discovered  during  surveys  of  moUusks  on 
bighorn  sheep  ranges  (Forrester  1 960, 1 962);  specific  collection  sites  provided  by  Forrester 
(1 960, 1 962)  are  somewhat  vague.  The  Prospect  Creek  site  in  Sanders  County  was  the  only 
one  known  in  Montana  at  the  time  of  publication  of  Pilsbry 's  monograph  (Pilsbry  1 948). 
Reported  elevations  of  sites  inldaho  range  between  488- 1707  m  (1600-5600  ft)  (Pilsbry 
1948,  H.  Reise  personal  communication),  the  Montana  sites  range  between  640-1494  m 
(2100-4900  ft). 

D.  Species  Abundance 

No  information,  although  it  appears  to  still  be  present  at  several  sites  in  Idaho  (Frest  and 
Johannes  1995),  including  as  recently  as  2001  (H.  Reise  personal  communication).  Pilsbry 
(1 948)  stated  it  was  often  abundant.  Montana  sites  have  not  been  revisited  in  decades. 

Current  Status 

A.  Why  Species  is  of  Conservation  Concern 

The  Sheathed  Slug  {Zacoleus  idahoensis)  is  a  Species  of  Concern  in  Montana  because  it  is  a 
regional  endemic  so  far  documented  at  only  four  sites  in  four  counties,  none  of  which  has  been 
revisited  in  recent  decades.  Population  sizes  and  trends  are  unknown,  but  habitat  loss  has 
occurred  throughout  the  historic  range  (Frest  and  Johannes  1 995). 

B.  Threats 

Habitat  occupied  by  Zacoleus  idahoensis  (moist  sites  in  moderate  elevation  mixed  conifer 
forest)  is  threatened  by  logging,  grazing,  fire,  trail  and  highway  expansion,  possibly  rural  home 
development,  and  possibly  recreation  and  weed  control.  The  impact  of  fire  retardant  on  this 
species  and  other  terrestrial  moUucks  is  unknown.  Little  is  known  about  the  biology  of  this 
species,  including  its  sensitivity  to  disturbance. 

C.  Distribution  Relative  to  Land  Allocations 

Documented  Montana  sites  are  on  lands  administered  by  the  Libby  Ranger  District,  Kootenai 
National  Forest  (1  site),  Thompson  Falls  Ranger  District,  Lolo  National  Forest  with  some 
private  in-holdings  (1  site),  Philipsburg  Ranger  District,  Beaverhead-Deerlodge  National  Forest 
(1  site),  and  State  of  Montana  (1  site);  the  Beaverhead-Deerlodge  site  may  be  on  Bureau  of 
Land  Management  lands. 


50 


Figure  12.  Distribution  of  Polygyrella  polygyrella  in  Montana. 


•     Polygyrella  polygyrella 
^^/Continental  Divide 
US  Forest  Service 


52 


SPECIES  ON  REVIEW 
SNAILS 

SPECIES:  Polygyrellapolygyrella  (Humped  Coin) 

Heritage  Rank:  GU,SU 
Natural  History 

A.  Taxonomy 

Family:  Ammonitellidae 

Polygyrellapolygyrella  (Bland  and  Cooper,  1 861) 

Originally  described  by  Bland  and  Cooper  (1 861)  as  Helix polygyrella,  with  later  placement 
by  Cooper  (1 868)  as  Helicodiscus polygyrella.  The  genus  is  monospecific  and  restricted  to 
interior  Pacific  Northwest. 

B.  Species  Description 

Morphology:  Pilsbry  (1 939)  describes  the  shell  as  "discoidal,  with  wide  umbilicus  about  one- 
third  of  the  diameter;  of  a  pale  greenish  yellow  tint,  somewhat  translucent,  glossy.  Spire  varies 
from  nearly  flat  to  convex,  of  very  closely  coiled  whorls.  Initial  2  to  3  whorls  smooth,  the  rest 
with  rather  strong  radial  ribs  which  become  obsolete  near  the  aperture . . .  Suture  impressed, 
descending  a  little  to  the  aperture.  Umbilicus  well-like,  enlarging  in  the  last  half  whorl.  Aperture 
lunate-triangular,  the  peristome  thickened  within;  parietal  wall  with  an  erect,  triangular  tooth 
connected  with  the  ends  of  the  lip.  Within  the  last  whorl  there  are  one  or  two  radial  rows  of 
three  teeth  each,  visible  through  the  shell"  (p.  558-559).  Shell  diameter  of  26  Idaho  specimens 
ranged  from  8.6  to  1 0.5  mm  (mean  =  9.7  mm),  but  diameter  of  specimens  from  other  localities 
ranges  to  13.0  mm.  Number  of  whorls  varies  from  6.5  to  8.5.  Shell  height  is  from  40-50%  of 
the  diameter.  Diameter  of  the  type  specimen,  presumably  from  Sanders  County,  Montana,  is 
11.5  mm,  height  5  mm  (Bland  and  Cooper  1 861).  Internal  anatomy  is  illustrated  and  described 
in  Pilsbry  (1939). 

Reproductive  biology:  Hermaphroditic,  based  on  internal  anatomy  (Pilsbry  1 939).  There  is  no 
description  of  reproductive  behavior  and  its  seasonal  occurrence.  Life  span  is  unknown.  Age/ 
size  at  reproductive  maturity  is  unknown. 

Ecology:  Often  found  in  moist  forests  of  Pseudotsuga  menziezn  and  Picea  engelmannii,  often 
in  association  with  outcrops  and  talus  of  various  rock  types  (Bland  and  Cooper  1 861 ,  Pilsbry 
1 939,  Frest  and  Johannes  1 995).  Inhabits  moss  and  decaying  wood  in  dampest  areas  of  forest 
cover  (Bland  and  Cooper  1 861 ,  Cooper  1 868);  moist  valley,  ravine,  and  talus  sites  are 


53 


preferred,  apparently  near  water  (Frest  and  Johannes  1 995).  There  is  no  information  on  food 
habits.  Associated  moUusk  species  include  the  slugs  Zacoleus  and  Hemphillia. 

C.  Range  and  Known  Sites 

Polygyrellapolygyrella  is  found  in  northwestern  Montana,  northern  Idaho,  and  the  Blue 
Mountains  of  extreme  southeastern  Washington  and  extreme  northeastern  Oregon  (Pilsbry 
1 939,  Frest  and  Johannes  1 995).  The  eastern  slope  of  the  Coeur  d' Alene  Mountains,  Sanders 
County,  Montana  is  considered  the  type  locality  (Pilsbry  1 939,  Frest  and  Johannes  1 995), 
although  the  original  description  (Bland  and  Cooper  1861)  places  the  locality  only  as  the  eastern 
slope  of  the  Coeur  d' Alene  Mountains  (later  identified  as  Montana  by  Cooper  1 868),  which  led 
others  to  place  the  type  locality  in  Idaho  (Elrod  1 902,  Henderson  1 93 6,  Coan  1981).  The  type 
locality  may  actually  be  somewhere  in  Mineral  County;  Cooper  traveled  along  the  road 
constructed  by  Lt.  John  Mullen  up  the  St.  Regis  River  from  its  confluence  with  the  Clark  Fork 
River  at  St.  Regis  (Coan  1981),  passing  through  Mullen  Gulch.  In  Montana,  this  species  is 
currently  recognized  from  four  sites  at  elevations  between  792  and  1097  m  (2600  and  3600  ft) 
in  two  counties:  Sanders  and  Mineral  (Fig.  12,  Appendix  B).  However,  Elrod  (1902)  and 
Pilsbry  (1 939)  note  an  unique  variety  oi Polygyrellapolygyrella,  named  montanensis,  found  in 
the  "Deer  Lodge  Valley"  sometime  prior  to  1 902  by  Mr.  Hemphill.  The  locality  is  not  listed  in 
Appendix  B,  but  indicates  that  the  species  may  also  be  present  in  Powell  or  Deer  Lodge 
counties.  Additional  locations  are  possible.  Requirements  may  be  similar  to  Radiodiscus 
abietum/judging  by  the  similarity  in  their  distributions. 

D.  Species  Abundance 

No  information.  A  few  Idaho  populations  were  still  extant  in  the  early  1 990 's  (Frest  and 
Johannes  1 995),  but  there  is  no  indication  that  the  species  has  been  found  in  Montana,  even  at 
the  known  localities,  in  recent  decades. 

Current  Status 

A.  Why  Species  is  of  Conservation  Concern 

The  Humped  Coin  (Polygyrellapolygyrella)  is  a  Species  on  Review  in  Montana  because  it  is  a 
regional  endemic  of  unknown  status  so  far  documented  at  only  four  (possibly  five)  sites  in  two 
Montana  counties,  despite  several  decades  of  collecting  in  the  region  by  Dr.  R.  B.  Brunson  and 
his  students.  There  is  evidence  of  extirpations  and  population  declines  in  other  states  (Frest  and 
Johannes  1 995).  Population  sizes  and  trends  in  Montana  are  unknown,  and  there  is  no 
evidence  that  the  snail  has  been  documented  in  Montana  in  recent  decades. 

B.  Threats 

Logging  and  grazing  over  most  of  the  known  range  are  probably  the  greatest  threats,  through 
alteration  of  appropriate  habitat.  However,  alteration  of  habitat  from  fire,  highway  and  road 


54 


construction,  rural  home  development  and  land  clearing  could  represent  threats,  as  could  fire 
suppression  retardants  and  chemical  methods  of  weed  control. 

C.  Distribution  Relative  to  Land  Allocations 

Documented  Montana  sites  are  on  lands  administered  by  the  Thompson  Falls  Ranger  District, 
Lolo  National  Forest  with  private  in-holdings  (1  site),  Superior  Ranger  District,  Lolo  National 
Forest  (1  possibly  2  sites),  and  1  site  on  private  land  near  Thompson  Falls.  The  vague  locality 
for  the  Deer  Lodge  Valley  site  precludes  assigning  ownership  to  the  lands  where  it  was  found. 


55 


Figure  13.  Distribution  of  Radiodiscus  abietum  in  IVIontana. 


•     Radiodiscus  abietum 
^^/Continental  Divide 
US  Forest  Service 


56 


SPECIES:  Radiodiscus  abietum  (Fir  Pinwheel) 

Heritage  Rank:  GU,SU 
Natural  History 

A.  Taxonomy 

Family:  Helicodiscidae 
Radiodiscus  abietum  Baker,  1930 

The  original  designation  and  placement  remain  valid  and  unchanged  (Pilsbry  1 948,  Frest  and 
Johannes  1995). 

B.  Species  Description 

Morphology:  Pilsbry  (1948)  describes  the  shell  as  "small  (6.7  mm),  subdiscoid,  umbilicate,  thin, 
but  with  heavy,  almost  opaque  epidermis.  Color:  light  chocolate-brown.  Whorls:  maximum  5 
3/4,  gradually  increasing  in  diameter,  well  rounded  but  markedly  flattened  above;  last  slightly 
descending;  suture  deep. . .  Sculpture  of  later  whorls:  growth-riblets  quite  low  but  angular  and 
sharply  defined,  markedly  and  broadly  concave  below  periphery . . .  Umbilicus:  about  6. 1  times 
in  maj .  diam.  of  shell;  with  almost  vertical  walls.  Aperture:  crescentric,  slightly  oblique . . ."  (p. 
658, 660).  Shell  diameter  is  4.9  to  6.7  mm,  shell  height  2.6  to  3.2  mm,  with  5.0  to  5.75  whorls 
(Pilsbry  1 948).  Diameter  of  1 5  "representative"  shells  from  seven  Montana  localities  ranged 
from  2.5  to  7.0  mm  (mean  =  5.1  mm);  shell  height  ranged  from  1 .4  to  4.0  mm  (mean  =  2.8 
mm);  number  of  whorls  ranged  from  3 .5  to  6.0  (Brunson  and  Russell  1 967).  Internal  anatomy 
is  illustrated  and  described  in  Pilsbry  (1 948). 

Reproductive  biology:  Hermaphroditic,  based  on  internal  anatomy  (Pilsbry  1 948).  There  is  no 
description  of  reproductive  behavior  and  its  seasonal  occurrence.  Life  span  is  unknown.  Age/ 
size  at  reproductive  maturity  is  unknown,  but  Pilsbry  (1 948)  indicated  the  type  specimen 
(diameter  4.9  mm,  5  whorls)  was  immature. 

Ecology:  Surprisingly  little  detailed  information  is  available.  Most  often  found  in  moist  and  rocky 
Douglas-fir  (Pseudotsuga  menziesii)  forest  at  mid-elevations  in  valleys  and  ravines  (Frest  and 
Johannes  1 995).  At  some  Montana  locations.  Western  Red  Cedar  (Thuja plicata)  formed  the 
canopy.  Often  this  species  is  found  in  or  near  talus  of  a  variety  of  rock  types  or  under  fallen 
logs  (Pilsbry  1948,  Brunson  and  Russell  1967,  Frest  and  Johannes  1995). 

C.  Range  and  Known  Sites 

Radiodiscus  abietum  is  known  from  extreme  northeastern  Oregon,  extreme  northeastern  and 
southeastern  Washington,  northern  Idaho,  and  northwestern  Montana  (Pilsbry  1 948,  Frest  and 
Johannes  1995).  In  Montana,  this  species  has  been  found  at  13  sites  in  six  counties:  Lake, 
Lincoln,  Mineral,  Missoula,  Ravalli,  and  Sanders  (Fig.  1 3,  Appendix  B).  All  sites  are  west  of 


57 


the  Continental  Divide  (Brunson  and  Russell  1967)  at  elevations  from  823  to  1707  m  (2700- 
5600  ft).  Requirements  may  be  similar  to  Polygyrellapolygyrella/judgmg  by  the  similarity  of 
their  distributions. 

D.  Species  Abundance 

No  information.  Usually  only  single  individuals  were  collected  at  the  Montana  sites  (Brunson 
and  Russell  1 967).  Frest  and  Johannes  (1 995)  consider  Radiodiscus  abietum  a  species  that 
was  once  common  and  widespread  that  is  now  much  more  rare. 

Current  Status 

A.  Why  Species  is  of  Conservation  Concern 

The  Fir  Pinwheel  {Radiodiscus  abietum)  is  a  Species  on  Review  in  Montana  because  it  is  a 
regional  endemic  of  unknown  status,  so  far  documented  at  1 3  sites  in  six  Montana  counties, 
despite  several  decades  of  collecting  in  the  region  by  Dr.  R.  B.  Brunson  and  his  students.  There 
is  evidence  of  extirpations  and  population  declines  in  other  states  (Frest  and  Johannes  1 995). 
Population  sizes  and  trends  in  Montana  are  unknown,  and  there  is  no  evidence  that  the  snail  has 
been  documented  in  Montana  in  recent  decades. 

B.  Threats 

Logging  and  grazing  over  most  of  the  known  range  are  probably  the  greatest  threats,  through 
alteration  of  appropriate  habitat.  However,  alteration  of  habitat  from  fire,  highway  and  road 
construction,  rural  home  development  and  land  clearing  could  represent  threats,  as  could  fire 
suppression  retardants  and  chemical  methods  of  weed  control. 

C.  Distribution  Relative  to  Land  Allocations 

Documented  Montana  sites  are  on  lands  administered  by  the  Confederated  Salish  and  Kootenai 
Tribes  (3  sites).  State  of  Montana  (1  site,  but  bounded  closely  by  the  Missoula  Ranger  District, 
Lolo  National  Forest),  Superior  Ranger  District,  Lolo  National  Forest  (1  site).  Darby  Ranger 
District,  Bitterroot  National  Forest  (3  sites).  Cabinet  Ranger  District,  Kootenai  National  Forest 
(2  sites),  Fisher  River  Ranger  District,  Kootenai  National  Forest  (1  site),  Libby  Ranger  District, 
Kootenai  National  Forest  (1  site),  and  the  Rexford  Ranger  District,  Kootenai  National  Forest 
(1  site). 


58 


Figure  14.  Distribution  of   Udosarx  lyrata  in  Montana. 


•     Udosarx  lyrata 
^^/Continental  Divide 
US  Forest  Service 


60 


SLUGS 


SPECIES:  Udosarx  lyrata  (Lyre  Mantleslug) 

Heritage  Rank:  G?TU,  SU  {U.  I  lyrata); 
G7TI,  SI  (airusselli) 

Natural  History 

A.  Taxonomy 

Family:  Arionidae 

Udosarx  lyrata  Webb,  1959 

The  original  species  determination  and  name  (Webb  1 959)  are  still  valid,  although  Udosarx 
lyrata  is  now  included  in  the  Arionidae  instead  of  Webb's  (1959)  tentative  placement  in  the 
Philomycidae  and  later  placement  (Russell  and  Webb  1 980)  with  the  Oreohelicidae.  Udosarx 
lyrata  russelli  is  a  subspecies  recognized  by  Russell  and  Webb  (1 980),  however,  they 
suggested  that  the  subspecific  designation  might  become  useless  once  new  material  from 
additional  localities  is  available  for  study.  Because  Webb's  (1 959)  species  description  did  not 
include  a  subspecies  name,  the  original  material  was  named  Udosarx  lyrata  lyrata  by  Russell 
and  Webb  (1 980).  The  genus  is  monospecific  and  restricted  to  the  interior  Pacific  Northwest. 

B.  Species  Description 

Morphology:  Webb  (1 959)  notes  that  the  external  form  of  Udosarx  lyrata  is  "much  as  in 
Zacoleus,  mantle  more  elongate,  back  more  carinate.  Respiratory  pore  posterior,  and 
posterior-edge  of  mantle  notched  (as  in  Zacoleusy  (p.  22).  Udosarx  differs  from  Zacoleus 
especially  in  the  shape  of  the  radular  teeth.  Webb  (1 959)  continues  that  Udosarx  is  about  half 
as  large  as  sexually  mature  Zacoleus.  The  body  is  "bluish  gray  with  a  lighter  tawny  zone  on  the 
keel  of  the  back.  Grooves  on  the  body  darker  than  adjoining  areas;  7-8  grooves  from  posterior 
mid-dorsum  to  posterior-edge  of  respiratory  pore,  much  as  in  Zacoleus.  Mantle  with  blackish 
lateral  lines.  Mid-mantle  to  front-edge  with  black  punctuations  vaguely  delineating  a  grid 
pattern.  Right  line  is  more  sinuous  than  the  left,  and  the  two  lateral  lines  for  a  lyre-shaped 
symbol — Whence  the  species  name,  lyrata.  The  intensity  of  coloration  may  vary"  (p.  22). 

An  alcohol-preserved  specimen  of  Udosarx  lyrata  russelli  measured  2.4  cm  in  length  (Russell 

and  Webb  1 980).  For  this  subspecies,  "the  head  and  neck  uniformly  dark  but  not  black 

The  mantle  is  attached  far  back,  so  that  the  anteriorly  a  long  free-lobe  overlies  the  neck.  The 
central  area  of  the  fore-half  of  the  mantle  bears  a  number  (18-30)  of  scattered  black  dots  and 
bars;  unlike  the  holotype,  the  black  lines  of  the  upper  sides  extend  forward  to  almost  the  front 
edge  of  the  mantle.  Otherwise  the  lines  are  as  in  the  holotype,  diverging  from  each  other  in  very 
short  arcs  to  give  the  lyre  shape.  The  posterior  mantle-edge  is  deeply  notched . . .  The 
respiratory  pore  is  posterior  and  on  the  right  edge  of  the  mantle.  The  mantle  covers  somewhat 


61 


less  than  half  the  body,  which  is  moderately  carinate  (not  keeled)  dorsally.  The  tail-tip  is  acutely 
pointed. . ."  (p.  8).  Internal  anatomy  is  illustrated  and  described  in  Webb  (1 959)  and  Russell 
and  Webb  (1 980);  the  latter  publication  also  includes  photographs  of  live  animals  that  clearly 
show  the  lyre-pattern  on  the  mantle. 

Reproductive  biology:  Hermaphroditic,  based  on  internal  anatomy  (Webb  1959,  Russell  and 
Webb  1 980).  Courtship  and  copulation  were  observed  in  captive  animals  in  November 
(Russell  and  Webb  1 980).  Otherwise  there  is  no  description  of  reproductive  behavior  and  its 
seasonal  occurrence.  Life  span  is  unknown.  Age/size  at  reproductive  maturity  is  unknown, 
although  presumably  the  individual  2.4  cm  in  body  length  (Russell  and  Webb  1 980)  was  mature. 

Ecology:  Found  in  moist  mixed-conifer  subalpine  forest,  preferably  in  moist  valleys,  ravines,  and 
talus  sites  (Webb  1 959,  Frest  and  Johannes  1 995).  Also  found  in  riparian  areas  with  a  canopy 
of  Picea  engelmannii,  Pseudotsuga  menziesn,  Populus  andAlnus  (W.  Leonard  personal 
communication).  The  subspecies  U.  I  ra^^^/// was  found  in  south-facing  open  P/a2i/^ 
ponderosa  forest  with  little  undergrowth  (Russell  and  Webb  1 980).  At  all  sites,  individuals 
were  located  on  the  undersurfaces  of  fallen  logs  or  within  nearly  completely  rotten  logs,  and 
under  rocks.  Animals  were  active  in  wet  and  cold  (1 0°C  [50°F])  conditions  (Webb  1 959, 
Russell  and  Webb  1 980);  captive  animals  preferred  temperatures  <21  °C  (70°F). 

C.  Range  and  Known  Sites 

Udosarx  lyrata  has  so  far  been  documented  only  in  northern  Idaho  and  northwestern  Montana 
(Frest  and  Johannes  1 995).  The  type  locality  is  near  Lolo  Pass,  but  on  the  Idaho  side  (Webb 
1 959).  In  Montana,  records  exist  for  only  three  sites  in  two  counties:  Missoula  and  Ravalli  (Fig. 
1 4,  Appendix  B).  The  two  Missoula  County  sites,  discovered  in  1 965  and  1 966  near  Potomac 
and  Gold  Creek  (Russell  and  Webb  1 980),  are  far  from  the  Ravalli  County  site,  discovered  at 
Bunkhouse  Creek  in  the  Bitterroot  Mountains  in  200 1  (W.  Leonard  personal  communication). 
Reported  elevations  are  1067-1524  m  (3500-5000  ft).  Additional  locations  are  likely  to  be 
discovered. 

D.  Species  Abundance 

Little  information.  Only  one  individual  was  found  at  the  Ravalli  County  site  (W.  Leonard 
personal  communication).  Russell  and  Webb  (1980)  reported  finding  1 7  individuals  at  the 
Potomac,  Missoula  County,  site  on  3  May  1 965,  several  individuals  on  2 1  November  1 965, 
and  3  individuals  on  5  May  1 966.  Two  individuals  were  found  at  the  Gold  Creek,  Missoula 
County,  site  on  5  May  1 966.  Russell  (Russell  and  Webb  1 980)  collected  an  individual  at  the 
species  type  locality  in  1 966,  almost  1 2  years  after  it  was  first  found  there  (Webb  1 959). 
Known  to  be  present  at  some  Idaho  sites  in  recent  years  (Frest  and  Johannes  1 995,  W. 
Leonard  personal  communication). 


62 


Current  Status 

A.  Why  Species  is  of  Conservation  Concern 

The  Lyre  Mantleslug  (Usosarx  lyrata)  is  a  Species  on  Review  in  Montana  because  it  is  a 
regional  endemic  of  unknown  status  so  far  documented  at  three  sites  in  two  Montana  counties, 
despite  several  decades  of  collecting  in  the  region  by  Dr.  R.  B.  Brunson  and  his  students.  There 
is  evidence  of  extirpations  or  population  declines,  largely  inferred  from  loss  of  habitat  (Frest  and 
Johannes  1 995).  Population  sizes  and  trends  in  Montana  are  unknown,  and  there  is  no 
evidence  that  the  Missoula  County  sites  have  been  resurveyed  in  recent  decades. 

B.  Threats 

Habitat  occupied  by  Udosarx  lyrata  (moist  sites  in  valley  and  mid-elevation  mixed  conifer 
forest)  is  threatened  by  logging,  grazing,  fire,  possibly  rural  home  development  and  road 
construction,  and  possibly  recreation  and  weed  control.  The  impact  of  fire  retardant  and 
chemical  means  of  weed  control  on  this  and  other  terrestrial  moUusk  species  is  unknown.  Little 
is  known  about  the  biology  of  this  species,  including  its  sensitivity  to  disturbance. 

C.  Distribution  Relative  to  Land  Allocations 

Documented  Montana  sites  are  on  lands  administered  by  the  Darby  Ranger  District,  Bitterroot 
National  Forest  (1  site).  Plum  Creek  Timber  Company  (1  site),  and  private  ownership  (1  site). 
The  type  locality  in  Idaho  is  4  km  (2.5  mi)  from  land  in  Montana  administered  by  the  Missoula 
Ranger  District,  Lolo  National  Forest  and  Plum  Creek  Timber  Company. 


63 


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Bartsch,  P.  1916.  Two  new  land  shells  from  the  western  states.  Proceedings  of  the  United  States 
National  Museum  51:331-333. 

Beetle,  D.E.  1957.  The  moUusca  of  Teton  County,  Wyoming.  The  Nautilus  71:12-22. 

Beetle,D.E.  1961.  MoUusca  of  the  Big  Horn  Mountains.  The  Nautilus  74:95-102. 

Beetle,  D.E.  1989.  Checklist  ofrecent  moUusca  of  Wyoming,  USA.  Great  Basin  NaturaUst  49: 637- 
645. 

Beetle,  D.E.  1997.  Recolonization  of  burned  aspen  groves  by  land  snails.  Yellowstone  Science 
5(summer):6-8. 

Berry,  S.S.  1913.  A  list  ofmoUusca  from  the  MusselsheU  Valley,  Montana.  The  Nautilus  26:130-131. 

Berry,  S.S.  1916.  Notes  on  moUusca  of  central  Montana.  The  Nautilus  29: 124-128. 

Berry,  S.S.  1919.  MoUusca  ofGlacier  National  Park.  Proceedings  ofthe  Academy  of  Natural 
Sciences  of  Philadelphia  71 : 1 95-205. 

Berry,  S.S.  1 955.  An  important  new  land  snail  from  the  Mission  Range,  Montana.  Bulletin  ofthe 
Southern  California  Academy  of  Sciences  54:17-19. 

Bland,  T,  and  J.  G.  Cooper.  1 861 .  Notice  of  land  and  freshwater  shells  collected  by  Dr.  J.  G.  Cooper 
in  the  Rocky  Mountains,  etc.,  in  1 860.  Annals  ofthe  Lyceum  of  Natural  History  of  New  York 

7:362-370. 

Boag,  D.  A.,  and  W.  D.  Wishart.  1 982.  Distribution  and  abundance  of  terrestrial  gastropods  on  a 

winter  range  of  bighorn  sheep  in  southwestern  Alberta.  Canadian  Journal  of  Zoology  60:2633- 
2640. 

Brunson,R.B.  1956.  The  mystery  of  Discus  brunsoni.  The  Nautilus  70:16-21. 

Brunson,  R.  B.,  and  N.  Kevern.  1 963 .  Observations  of  a  colony  of  Magnipelta.  The  Nautilus  77:23- 
27. 

Brunson,  R.B.,  and  U.  Osher.  1957.  Haplotrema  from  wQstemMontSimi.  The  Nautilus  70:121-123. 

Brunson,  R.  B.,  and  R.  H.  Russell.  1 967.  Radiodiscus,  new  to  moUuscan  fauna  of  Montana.  The 
Nautilus  81:18-22. 


64 


Carlson,  J.  2003.  MontanaAnimal  Species  of  Concern.  Montana  Natural  Heritage  Program  and 

Montana  Fish,  Wildlife  and  Parks,  Helena,  Montana.  1 4  pp. 
Coan,  E.  1981.  James  Graham  Cooper,  pioneer  western  naturalist.  University  Press  of  Idaho, 

Moscow,  ID.  255  pp. 

Cooper,  J.  G.  1868.  The  shells  of  Montana.  American  Naturahst  2:486-487. 

Elrod,M.J.  1901a.  Montana  shells.  Rocky  Mountain  Magazine  2:691-697. 

Elrod,M.  J.  1901b.  Limnological  investigations  at  Flathead  Lake,  Montana,  and  vicinity,  July,  1899. 
Transactions  of  the  American  Microscopical  Society  22:63-80. 

Elrod,M.J.  1901-1902.  Collecting  shells  in  Montana.  The  Nautilus  15:86-89, 103-104, 110-112, 
129-130. 

Elrod,  M.  J.  1 902.  Abiological  reconnoissance  in  the  vicinity  of  Flathead  Lake.  University  of 
Montana  Bulletin  No.  10,  Biological  Series  No.  3. 

Elrod,  M.J.  1903a.  l<iotQS  on  PyramidulaelrodiVils.  The  Nautilus  16:109-112. 

Elrod,  M.J.  1903b.  Montana  shQlls-Pyramidulastrigosa.  The  Nautilus  17:1-6. 

Fairbanks,  H.L.I  980.  Morphological  notes  on  Oreohelix  amariradix  Pilsbry,  1 934  (Pulmonata: 
Oreohelicidae).  The  Nautilus  94:27-30. 

Fairbanks,  H.  L.  1984.  Anew  species  of  Oreohelix  (Gastropoda:  Pulmonata:  Oreohelicidae)  from  the 
Seven  Devils  Mountains,  Idaho.  Proceedings  of  the  Biological  Society  of  Washington  97: 1 79- 
185. 

Fairbanks,  H.  L.  2002.  The  reproductive  anatomy,  taxonomic  status,  and  range  of  Oreohelix  alpina 
(Elrod,  1901)  (Gastropoda:  Pulmonata:  Oreohelicidae).  The  Nautilus  116:in  press. 

Forrester,  D.  J.  1 960.  Apreliminary  investigation  of  the  protostrongylin  lungworm-bighom  sheep 
relationships  in  Montana.  M.S.  thesis,  Montana  State  University,  Missoula.  79  pp. 

Forrester,  D.  J.  1 962.  Land  moUusca  as  possible  intermediate  hosts  of  Protostrongylus  stilesi,  a 
lungworm  of  bighorn  sheep  in  western  Montana.  Proceedings  of  the  Montana  Academy  of 
Sciences  22:82-92. 

Frest,  T.  J.,  and  E.  J.  Johannes.  1 993 .  Land  snail  survey  of  the  Black  Hills  National  Forest,  South 

Dakota  and  Wyoming.  Final  report  to  USDA  Forest  Service,  Black  Hills  National  Forest  and 
USDI  Fish  &  Wildhfe  Service,  South  Dakota  State  Office.  1 56  pp.  +  appendices. 

Frest,  T.  J.,  and  E.  J.  Johannes.  1 995.  Interior  Columbia  Basin  moUusk  species  of  special  concern. 
Final  Report  to  Interior  Columbia  Basin  Ecosystem  Management  Project.  Deixis  Consultants, 


65 


Seattle.  274  pp. 
Henderson,  J.  1924.  MoUuscaofColorado,  Utah,  Montana,  Idaho,  and  Wyoming.  The  University  of 
Colorado  Studies  13:65-223. 

Henderson,  J.  1933.  MoUusca  of  the  Yellowstone  Park,  Teton  Park  and  Jackson  Hole  region.  The 
Nautilus47:l-3. 

Henderson,  J.  1 936.  MoUusca  of  Colorado,  Utah,  Montana,  Idaho,  and  Wyoming-supplement.  The 
University  of  Colorado  Studies  23:81-145. 

Hendricks,  P.  1998.  Rediscovery  of  D/^ct/^ /)rt//7^o^/ Berry,  1955  and  Oreohelix  alpina  (Elrod, 

1 90 1 )  in  the  Mission  Mountains,  Montana,  with  comments  on  Oreohelix  elrodi  (Pilsbry,  1 900). 
The  Nautilus  112:58-62. 

Karlin,  E.J.  1 96 1 .  Ecological  relationships  between  vegetation  and  the  distribution  of  land  snails  in 
Montana,  Colorado  and  New  Mexico.  American  Midland  Naturalist  65 :60-66. 

Leonard,  W.  P.,  and  K.  Ovaska.  2002.  Reproduction  of  the  Malone  jumping-slug,  Hemphillia 

malonei  Vilshry,  1917  (MoUusca:  Gastropoda:  Arionidae):  laboratory  observations.  Nemouria 
45:1-15. 

Niwa,  C.  G,  R.  E.  Sandquist,  R  Crawford,  and  1 8  others.  2001 .  Invertebrates  of  the  Columbia  River 
basin  assessment  area.  Gen.  Tech.  Rep.  PNW-GTR-5 12.  Portland,  OR:  U.S.  Department  of 
Agriculture,  Forest  Service,  Pacific  Northwest  Research  Station.  74  pp. 

Ovaska,  K.,  L.  Chichester,  H.  Reise,  W.  P.  Leonard,  and  J.  Baugh.  2002.  Anatomy  of  the  dromedary 
jumping-slug,  Hemphillia  dromedariusBmnson,  1972  (Gastropoda:  Stylommatophora: 
Arionidae),  with  new  distributional  records.  The  Nautilus  1 1 6:89-94. 

Pilsbry,  H.  A.  1900.  Notices  of  new  American  snails.  The  Nautilus  14:40-41 

Pilsbry,  H.  A.  1912.  Two  newAmerican  land  shells  collected  by  Messrs.  Hebard  and  Rehn.  The 
Nautilus  26:88-90. 

Pilsbry,  H.  A.  1 933 .  Notes  on  the  anatomy  of  Oreohelix, — III,  with  descriptions  of  new  species  and 
subspecies.  Proceedings  of  the  Academy  of  Natural  Sciences  of  Philadelphia  85:383-410. 

Pilsbry,  H.  A.  1 939.  Land  moUusca  of  North  America  (north  of  Mexico),  Volume  I  Part  1 .  The 
Academy  of  Natural  Sciences  of  Philadelphia  Monographs  Number  3  (1 ):  1  -573 . 

Pilsbry,  H.  A.  1948.  Land  moUusca  ofNorth  America  (north  ofMexico),  Volume  II  Part  2.  The 
Academy  of  Natural  Sciences  of  Philadelphia  Monographs  Number  3  (2) :  52 1  - 1 1 1 3 . 

Pilsbry,  H.  A.  1 953 .  Magnipelta,  a  new  genus  of  Arionidae  from  Idaho.  The  Nautilus  67:37-3  8. 


66 


Pilsbry,  H.  A.,  and  R.  B.  Bmnson.  1 954.  The  Idaho-Montana  slug  Magnipelta  (Arionidae).  Notulae 
Naturae  262:1-6. 

Piatt,  T.  R.  1 980.  Observations  on  the  terrestrial  gastropods  in  the  vicinity  of  Jasper,  Alberta 
(Canada).  The  Nautilus  94: 1 8-21 . 

Russell,  R.  H.,  and  R.  B.  Brunson.  1967.  Acheck-list  of  molluscs  of  Glacier  National  Park,  Montana. 
Sterkiana26:l-5. 

Russell,  R.  H.,  and  G.  R.  Webb.  1980.  The  slug  Udosarx  lyrata:  additional  data  on  distribution, 
anatomy,  and  taxonomy.  Gastropodia2:8-10. 

Squyer,H.  1894.  List  ofshells  from  the  vicinity  of  Mingusville,  Montana.  The  Nautilus  8:63-65. 

Vanatta,E.  G  1914.  Montana  shells.  Proceedings  ofthe  Academy  ofNatural  Sciences  of  Philadelphia 
66:367-371. 

Webb,  G  R.  1959.  Two  new  north-western  slugs,  Udosarx  lyrata  and  Gliabates  oregonia. 
Gastropodia  l(3):22-23, 28. 

Webb,  G  R.,  and  R.  H.  Russell.  1 977.  Anatomical  notes  on  a  Magnipelta:  Camaenidae? 
Gastropodia  1(10):107-108. 


67 


APPENDIX  A.    GLOBAL/STATE  RANK  DEFINITIONS 


Heritage  Program  Ranks 

The  international  network  of  Natural  Heritage  Programs  employs  a  standardized  ranking  system  to 
denote  global  (range-wide)  and  state  status  (NatureServe  2002).  Species  are  assigned  numeric  ranks 
ranging  from  1  (critically  imperiled)  to  5  (demonstrably  secure),  reflecting  the  relative  degree  to  which 
they  are  "at-risk".  Rank  definitions  are  given  below.  Anumber  of  factors  are  considered  in  assigning 
ranks — the  number,  size  and  distribution  of  known  "occurrences"  or  populations,  population  trends  (if 
known),  habitat  sensitivity,  and  threat.  Factors  in  a  species'  life  history  that  make  it  especially  vulnerable 
are  also  considered  (e.g.,  dependence  on  a  specific  pollinator). 

Rank  Definitions 

G 1  S 1  Critically  imperiled  because  of  extreme  rarity  and/or  other  factors  making  it  highly 

vulnerable  to  extinction. 

G2  S2  Imperiled  because  of  rarity  and/or  other  factors  making  it  vulnerable  to  extinction. 

G3  S3  Vulnerable  because  of  rarity  or  restricted  range  and/or  other  factors,  even  though  it  may 

be  abundant  at  some  of  its  locations. 

G4  S4  Apparently  secure,  though  it  may  be  quite  rare  in  parts  of  its  range,  especially  at  the 

periphery. 

G5  S5  Demonstrably  secure,  though  it  may  be  quite  rare  in  parts  of  its  range,  especially  at  the 

periphery. 

GU  SU  Possibly  imperiled,  but  status  uncertain;  more  information  needed. 

GA  S A  Native  in  nearby  states,  but  in  Montana  believed  to  be  accidentally  introduced, 

deliberately  planted,  or  escaped  from  plantings. 

GH  SH  Historical,  known  only  from  records  over  50  year  ago;  may  be  rediscovered. 

GX  SX  Believed  to  be  extinct;  historical  records  only. 

Combination  Ranks 

G#G#  or  S#S#  Indicates  a  range  of  uncertainty  about  the  rarity  of  the  species. 

Subranks 

T#  Rank  of  a  subspecies  or  variety;  appended  to  the  species'  global  rank  of  the  full 

species,  e.g.  G4T3. 

Qualifiers 

Q  Taxonomic  questions  or  problems  exist,  more  information  needed;  appended  to  the 

global  rank,  e.g.  G3Q. 

?  Denotes  uncertainty  or  for  numeric  ranks,  inexactness. 

A-1 


APPENDIX  B.    LOCALITY  AND  COLLECTION  RECORDS  FOR  15 
TERRESTRIAL  MOLLUSK  TAXA  OF  CONSERVATION  CONCERN  IN 

MONTANA 


Species 


Location 


TRS 


Elev  (ft)       County 


Date 


Habitat 


Notes^ 


Discus  brunsoni 


Discus  stiimeki 


McDonald  Lake,    T19N,R19W, 
Mission  Mtns        sec  1 1 NE 


3700 


Lake         26  Aug.  1948;  23      diorite  talus,  TYPE      Berry  1955,  Brunson 


W  of  Nurses 
Lakes 


T3S,R12E,  sec 
30SWNE 


6360 


Park 


June 

1950;  1  June 

LOCALITY 

1956,  Hendricks  1998; 

1954 

4  May,  2  July 

CAS  #1264413;  FMNH 

1955 

16  May 

#'s  98033,  108561; 

1957 

27  April 

USNM#  673345 

1960 

16  and  29 

(paratype);  Hendricks 

May  1964;  1  and 

specimens 

10  July  1997 

2  August,  2000 

aspen 

stand 

Hendricks  record 

Discus  stiimel<i 
Discus  stiimel<i 

Discus  sliimel<i 
Discus  sliimel<i 


Beaver  Creek,  T28N,R16E,  sec      4240 

Bears  Paw  Mtns  3NWNE 

falls  of  Natural  T3S,R12E,  sec 

Bridge,  Boulder  26NW 

River,  Absaroka 

Mtns. 

E  of  Kootenai  T31N,R32W, 

Falls  sec  15 


Gallatin  River 
corridor 


T6S,R4E,  sec 
22 


IHempliillia  danieisi  Bunkhouse  T3N,R21W,  sec 

Creek,  Bitterroot  7  middle 
Mtns 


l-iempiiillia  danieisi  Camas  Creek, 
Bitteroot  Mtns 

l-lempliillia  danieisi  Mill  Creek, 

Bitterroot  Mtns 

Hemphillia  danieisi  Medicine  Hot 
Springs, 
Bitterroot  Mtns 


Hill  20  June,  1997 

5100       Sweetgrass   ?? 


2100 


6000 


Lincoln       17  Sept.,  1959 
Gallatin       23  April,  1960 


5000 


T5N,R21W,  sec  ca. 

33SW  4800? 

T6N,R22W,  sec  4950 

1NENE 

T1N,R20W,  sec  4400 

12SW 


aspen  stand 

limestone,  with 
Doug-fir  cover 


Ravalli 

26  July,  2001 

nparian  spruce, 
Doug-fir, 
Cottonwood,  alder 

Ravalli 

12  May  1912;  7 

riparian  mixed 

October  2001 

conifer/deciduous, 
TYPE  LOCALITY 

Ravalli 

20  Oct.,  2001 

streamside,  under 
cobble 

Ravalli 

1912 

Hendricks  record 
Pilsbry  1948 


Forrester  1960;  FMNH 
#108487:  Kootenai 
Falls  sheep  range 
Forrester  1960;  USNM 
#762513;  Clyde 
Senger  specimen, 
FMNH  #108538: 
Gallatin  sheep  range 
Bill  Leonard  record; 
photo 


Pilsbry  1948;  ANSP# 
110052  (holotype); 
Heike  Reise  record 
B.  Maxell  record; 
Hendricks  specimen 
Pilsbry  1948 


B-1 


Species 


Location 


TRS 


Elev  (ft)       County 


Date 


Habitat 


Notes^ 


Hemphlllla  danieisi  N  end  Ward  Mtn, 

T5N,R21W,  sec 

4825 

Ravalli 

21  April,  1912 

Pilsbry  1948;  ANSP# 

Bitterroot  Mtns 

17NW? 

110053 

Magnipelta 

Thompson  River 

T24N,R27W, 

3140 

Sanders 

16  May,  2001 

shrubby 

Hendricks  record; 

mycophaga 

bottom,  3  mi  S  of 
Bend 

^sec12NWNE 

willow/dogwood, 
Ribes,  snowberry; 
scattered  ponderosc 
pine  and  Douglas-fir 
nearby 

photo 

Magnipelta 

Little  Park  Creek 

,  T12N,R18W, 

4300 

Missoula 

24  May  1998;  26 

riparian  alder. 

Hendricks  record; 

mycophaga 

Sapphire  Mtns 

secSONESW 

Sept.  2000 

spruce,  subalpine  fir  photo 

Magnipelta 

Marten  Creek 

T25N,R33W, 

2500 

Sanders 

7  May,  1999 

grand  fir,  alder 

Hendricks  record; 

mycophaga 

sec25SESE 

photo 

Magnipelta 

Deer  Creek, 

T12N,R18W, 

4100 

Missoula 

26  May  and  14 

Doug-fir,  spruce. 

Pilsbry  and  Brunson 

mycophaga 

Sapphire  Mtns 

sec7NENW 

June  1954;  29 

subalpine  fir. 

1954,  Brunson  and 

April-23  Sept.  1957  western  larch. 

Kevern1963;  FMNH 

ponderosa  pine 

#108562 

Magnipelta 

Red  Meadow 

T35N,R23W, 

ca.  5200 

Flathead 

31  July,  1951 

subalpine  fir- 

Pilsbry  and  Brunson 

mycophaga 

Lake 

sec  34NW 

whitebark  pine 

1954;  Brunson  catalog 
#M6151 

Magnipelta 

centered  on 

T34N,R29W, 

3500? 

Lincoln 

1959? 

Forrester  1960,1962: 

mycophaga 

McGuire  Creek 

sec  24 

centered  on  Ural- 
Tweed  sheep  range. 
Inch  and  McGuire 
Mtns. 

Oreohelix  alpina 

above  Lower 

T21N,R16W, 

7200 

Missoula 

lOAug.  1975;  11 

limestone  talus 

Fairbanks  2002; 

Rumble  Lake, 

sec  36SESW 

Sept.  2000 

Hammer  and 

Swan  Mtns 

Fairbanks  specimens; 
Hendricks  specimens 

Oreohelix  alpina 

E.  St  Marys  Pk, 

T18N,R18W, 

8900- 

Lake 

15  July  1900;  27 

alpine  limestone 

Elrod1902,  1903b; 

Mission  Mtns 

sec21SW 

9400 

Aug.  1997 

talus:  TYPE 
LOCALITY 

Hendricks  1998; 
FMNH  #108485 

Oreohelix  alpina 

West  McDonald 

T19N,R19W, 

7400- 

Lake 

22  July,  1900 

limestone  talus. 

Elrod1902,  1903b 

Peak,  Mission 

sec  24SE 

8000 

west  ridge  crest 

Mtns. 

Oreohelix  alpina 

McDonald  Peak, 
120  ft  below 
summit  on  S 
ridge 

T19N,R18W, 
sec29NWNE 

9700 

Lake 

18  Sept.,  1952 

limestone  talus 

J.  Chapman  specimen, 
FMNH  #108486 

B-2 


Species 


Location 


TRS 


Elev  (ft)       County 


Date 


Habitat 


Notes^ 


Oreohelix  alpha      McDonald  Peak;  T19N,R18W, 

above  Duncan  sec  30NE 
Lake 

Oreohelix  4.5-4.6  mi  W  of  T12N,R21W, 

amariradix  Lolo  along  US  sec  36SWSE 

12 


Oreohelix 
amariradix 


near  Lolo  Creek, 
across  from 
other  location 


T12N,R21W, 
sec36SWNE 


8500  Lake  2  Aug.,  1949 


3500         Missoula      20  July  1902;  9 

July  1950;  23  and 
30  May  1976;  29 
May  1977;  March 
1978 


3500         Missoula      5  June,  1976 


limestone  talus 


small  talus  slides  on 
N  slope  opposite  Ft. 
Fizzle;  in  ponderosa 
pine,  serviceberry, 
ninebark,  bunch 
grasses.  TYPE 
LOCALITY 
talus  slope  (in 
ponderosa  pine?) 


Brunson  catalog 
#M31349 

Fairbanks  1 980;  ANSP 
#  78740  (holotype), 
345588,  347820; 
FMNH#  74757,  84740 


Fairbanks  record 


Oreohelix 
carinifera 

Oreohelix 
carinifera 


Oreohelix 
carinifera 


Oreohelix 
carinifera 


Oreohelix  eirodi 


old  Byrne 
Resort,  Nimrod 
Hot  Springs 
Grouse  Creek 


Wet  Mulkey 
Gulch 


Garrison  Jet. 


Goat  Creek, 
Swan  Mtns 


T11N,R15W, 
sec14SESW 

T11N,R15W, 
sec  35/36S 


T12N,R13W, 
sec  32SENW 


T9N,R10W, 

sec14SofSE, 

sec23NofNE 


T23N,R17W, 
sec12NENW 


4100  Granite       13  July,  1975 


4300?         Granite       15  Nov.,  1975 


4850  Granite       3  Aug.  2002 


4300  Powell        1907;  1909;  4 

Sept.  1931;  25 
Aug.  1934;  7  July 
1947;  28  April 
1960;  17  July 
1976;  28  May  1977 

4250  Lake         9  June,  1999 


small  rock  outcrops 
above  pond 

sandy  limestone,  S 
facing  slopes 
w/juniperand  Doug- 
fir 

sandy  limestone,  S 
facing  slope,  open 
Doug.  Fir  canopy 
with  common  juniper 
in  understory 
S  facing  limestone 
slope,  on  surface  of 
outcrop  and  among 
junipers:  TYPE 
LOCALITY 


Fairbanks  record 


Fairbanks  record 


Hendricks  specimens 
(MTHP  4293);  dead 
shells 


argillite  talus 


ANSP  #'s  99253 
(paratypes),  345537, 
A14840;  FMNH  #'s 
84747,97987,98161, 
111794 

Hendricks  specimens 


Oreohelix  eirodi 


Lion  Creek,  T22N,R17W,  3600- 

Swan  Mtns  sec  11SW-13NE     4000 


Lake         ca.  1975;  25  Sept.    argillite  talus 
1997;  19  May  1999 


Fairbanks  1984; 
Hendricks  specimens 


B-3 


Species 


Location 


TRS 


Elev  (ft)       County 


Date 


Habitat 


Notes^ 


Oreohelix  eirodi 

McDonald  Lake, 

T19N,R19W, 

3700 

Lake 

July  1899;  July 

argillite  and  diorite 

Elrod1902,  1903a, 

Mission  Mtns 

secllNE 

1900;  June  1901; 
1902;  16  May,  7 
and  17  July,  7  Aug. 
1947;  26  Aug. 
1948;  7  Sept. 
1950;  2  Oct.  1955; 
29  June  1956;  11 
May  1959;  27  April 
1960;  10  June,  1 
July  1997 

talus:  TYPE 
LOCALITY 

Pilsbry  1939, 
Hendricks  1998;  ANSP 
#'s  78740  (lectotype), 
348135,  346218, 
345811;  FMNH#'s 
40079, 40080,  60312, 
74395, 74754,  86584, 
90351,90352,90492, 
90527,  97864,  98120, 
117891,  146468, 
172603;  USNM  # 
160833 

Oreohelix  strigosa 

1  mi  E  Piper 

T14N,R20E,  sec 

4500 

Fergus 

12  Sept.,  1944 

SW  facing  slope. 

USNM  #  592753 

berryi 

9SE 

under  creeping 
juniper 

Oreohelix  strigosa 

"vicinity  of 

T6S,R10E,  sec 

6200 

Park 

1994 

Frest  and  Johannes 

berryi 

Montanapolis" 

19 

1995 

Oreohelix  strigosa 

7miS 

T14N,R19E,  sec 

4250 

Fergus 

13  Sept.,  1944 

S  facing  slope 

USNM  #  592752 

berryi 

Lewistown,  near 
Big  Spring 

5SE 

Oreohelix  strigosa 

Half  Moon  Pass, 

T12N,R19E,  sec 

7300 

Fergus 

?? 

USNM  #477463 

berryi 

Big  Snowy  Mtns. 

28SW 

Oreohelix  strigosa 

Dry  Pole 

T12N,R17E 

5500- 

Fergus 

?? 

USNM  #477391 

berryi 

Canyon,  Big 
Snowy  Mtns. 

6500 

Oreohelix  strigosa 

Swimming 

T11N,R19E,  sec 

5880 

Golden 

4  July,  1914 

TYPE  LOCALITY 

see  Pilsbry  1933  for 

berryi 

Woman  Canyon, 
Big  Snowy 
Mtns.,  about  half 
a  mile  above  the 
mouth 

16NW 

Valley 

location 

Oreohelix  strigosa 

Blake  Creek 

T11N,R18E 

Fergus 

14  Sept.,  1919 

berryi 

Canyon,  Big 
Snowy  Mtns. 

Oreohelix  strigosa 

Judith  Mtns. 

T16N,R19E,  sec 

5320 

Fergus 

20  April,  1998 

rocky  slope  of 

Hendricks  specimens: 

berryi 

16SENE 

limestone  in  old  burn  ID  not  confirmed,  but 

likely 


B-4 


Species 


Location 


TRS 


Elev  (ft)       County 


Date 


Habitat 


Notes^ 


Oreohelix  strigosa 
berryi 

Oreohelix  strigosa 
berryi 


Oreotielix  yavapai 
mariae 


Polygyrella 
polygyrella 


Polygyrella 
polygyrella 


Polygyrella 
polygyrella 

Polygyrella 
polygyrella 


Prophysaon 
humile 


Timber  Creek 
Canyon,  Big 
Snowy  Mtns. 
W of  head, 
Middle 
Cottonwood 
Canyon,  Big 
Snowy  Mtns. 
1/4  mi  from 
mouth  of  Squaw 
Creek,  and  also 
N  side  of  canyon 

3-6  mi  up 
Prospect  Creek 
W  of  Thompson 
Falls,  Coeur 
d'Alene  Mtns. 
2mi.  W 

Thompson  Falls 
at  confluence  of 
Clear  Cr.  With 
Prospect  Cr. 
West  Fork  Big 
Creek,  DeBorgia 


T11N,R18E 


T12N,R18E,  sec  ca. 
26? 


Fergus       ?? 
8000        Fergus       ?? 


T4S,R4E,  sec 
34SWSW 


T21N,R30W, 
sec  21-23 


T21N,R30W,sec 
.  13NESW 


T19N,R30W,sec 
.30SE? 


2600 


Sanders      1  May,  1949 


E  slope  of  Coeur  ??  (?  SW  of 


d'  Alene  Mtns. 


Yellow  Bay  Biol. 
Stn. 


DeBorgia; 
possibly  Dry  Cr., 
or  NW  of  St. 
Regis  in  Mullen 
Gulch?) 
T24N,R19W, 
sec.  4NE 


3600?  Mineral       17  May,  1964 


??  ?  Sanders    Sept.,  1860 

or  Mineral  ? 


ca.  3000  Lake         11  July.  1960 


Berry  specimen 
Berry  specimen 


5600  Gallatin       prior  to  1 91 6;  30 

Aug.  1925;  30  Aug. 
1939;  8  July  1947; 
4  May  1976 

2800         Sanders      ??(priorto  1936) 


S-facing  open  Bartsch  1916;  USNM  # 

grassy  slope  at  base  522585,  215132  (types 
of  outcrop:  TYPE 
LOCALITY 


moss  and  decaying 
wood  in  dampest 
parts  of  spruce 
forest 


in  moss  and 
decaying  wood  in 
damp  spruce  forest: 
TYPE  LOCALITY 


and  paratypes);  ANSP 
#345575,  113374 
(paratype) 
Henderson  1936, 
Baker  record  in  Pilsbry 
1939 


Brunson  catalog 
#M  10049 


Brunson  catalog 
#M2964,  M3364:  TRS 
not  given 

Bland  and  Cooper 
1861;  Coan  1981 
gives  type  locality  as  in 
ID,  but  Pilsbry  1939 
lists  Sanders  Co.,  MT: 
Cooper  1868  gives  MT 
FMNH  #119010 


Radiodiscus 
abietum 


between  Leigh 
Lake  trail  and 
Leigh  Creek, 
Cabinet  Mtns. 


T28N,R31W,sec 
.6NWNE 


3900 


Lincoln       27  July,  1960 


under  log 


Brunson  and  Russell 
1967 


B-5 


Species 


Location 


TRS 


Elev  (ft)       County 


Date 


Habitat 


Notes^ 


Radiodiscus 
abietum 

Radiodiscus 
abietum 

Radiodiscus 
abietum 


4  mi.  W  Noxon 


T26N,R33W,sec 
.17SESE 


T26N,R32W,sec 
.20NW 


Government 

Creek  at  Noxon, 

Cabinet  Mtns. 

South  Crow  T20N,R19W,sec 

Cirque,  Wend  of  .  10SESE 

Schwartz  Lk., 

Mission  Mtns. 


3000 


2700 


3950 


Sanders 


Sanders 


Lake 


2  May,  1965 
20  June,  1956 
7  July,  1960 


Brunson  and  Russell 
1967 

Brunson  and  Russell 
1967;  Brunson  catalog 
gives  26  June 
Brunson  and  Russell 
1967;  FMNH  #105851 


Radiodiscus 
abietum 

Radiodiscus 
abietum 


Radiodiscus 
abietum 


McDonald  Lake 
at  dam.  Mission 
Mtns 

McDonald 
Cirque  above 
McDonald  Lake, 
Mission  Mtns. 


Crystal  Lake 
Trail,  ca.  5  mi. 
DeBorgia 


T19N,R19W,sec 
.10NENE 

T19N,R19W,sec 
.  11NW 


3600 


3600 


Lake    19  June,  1960 


Lake    11  May  1959,  17 
and  23  June  1960, 
16  May  1964 


wet  bank  W  side  of 
talus  slide 


T18N,R30W,sec 
.15SW 


4000 


Mineral       17  Oct.,  1965 


under  fallen  logs  in 
cedar  forest 


FMNH  #110641 


Brunson  and  Russell 
1967;  elev  must  be  in 
sec.  11,  not  sec.  2  as 
given  for  1960  record; 
1959  and  1964 
records  not  published 
(Brunson  catalog 
#M1259andM664) 
Brunson  and  Russell 
1967;  elev  given  as 
2800'  with  no  TRS  but 
trail  starts  higher  up 


Radiodiscus 
abietum 

Radiodiscus 
abietum 

Radiodiscus 
abietum 


Deep  Creek, 
Bitterroot  Mtns. 


T13N,R21W,sec 
.20NW 


T5N,R22W,sec. 
35SWSE 


N.  Fork  Lost 

Horse  Cr., 

Bitterroot  Mtns. 

Lost  Horse  T4N,R22W,sec. 

Creek,  Bitterroot  6NWNW 

Mtns. 


4000         Missoula      11  May,  1957 

5600  Ravalli        May,  1960 

5000  Ravalli       5  June,  1960 


Brunson  and  Russell 
1967 

Brunson  and  Russell 
1967 

Brunson  and  Russell 
1967 


B-6 


Species 


Location 


TRS 


Elev  (ft)       County 


Date 


Habitat 


Notes^ 


Radiodiscus 
abietum 


Radiodiscus 
abietum 

Radiodiscus 
abietum 


Sleeping  Child 
Cr.  below 
Sleeping  Child 
Hot  Springs, 
Sapphire  Mtns. 
SW  shoulder 
Stenerson  Mtn. 

Tweed  Creek 


T4N,R19W,sec. 
7NW 


4550 


T32N,R28W,sec  ca.  5000 
.3 

T34N,R29W,sec  ca.  4000 
.35 


Ravalli       31  December, 
1965 


Lincoln       15  Sept.,  1959 


Lincoln       18  July,  1962 


Brunson  and  Russell 
1967 


Forrester  specimen  in 
FMNH  #108508:  Ural- 
Tweed  sheep  range 
FMNH  #117379;  Ural- 
Tweed  sheep  range 


Udosarx  lyrata 


Udosarx  lyrata 


Udosarx  lyrata 
russelli 


Zacoleus 
idahoensis 


Bunkhouse 
Creek,  Bitterroot 
Mtns 

ca.  2  mi.  N  Twin 
Creeks  Lumber 
Camp,  near 
wetland  and  F.S. 
road 

1  miWof 
Potomac 


E  of  Kootenai 
Falls,  Purcell 
Mtns. 


T3N,R21W,  sec       5000 
7  middle 


Ravalli       26  July,  2001 


T14N,R17W,sec 
25SW 


4000         Missoula      5  May,  1966 


T13N,R16W,  3500 

sec  10  (possibly 
sec  15) 


T31N,R32W,  2100 

sec  15 


Missoula 


3  May  and  21  Nov. 
1965,  5  May  1966 


Lincoln       1959? 


nparian  spruce, 
Doug-fir, 

Cottonwood,  alder 
under  rocks  near 
spring-fed  0.5  acre 
pond; open 
coniferous 
ponderosa  pine  and 
Douglas-fir 
S  slope  above  Union 
Creek,  under  logs; 
ponderosa  pine  and 
undergrowth:  TYPE 
LOCALITY  for 
subspecies 


Bill  Leonard  record; 
photo 

Russell  and  Webb 
1980;  in  Dick  Russell 
unpublished  notes  and 
correspondance 


Russell  and  Webb 
1980;  ANSP#  358248 


Forrester  1960,  1962: 
Kootenai  Falls  sheep 
range 


Zacoleus 
idahoensis 

Zacoleus 
idahoensis 


centered  on  T7N,R16W,  sec 

Squaw  Rock  CG,  21 
Sapphire  Mtns. 


3-6  mi  up 
Prospect  Creek 
W  of  Thompson 
Falls,  Coeur 
d'Alene  Mtns. 


T21N,R30W, 
sec  21-23 


4900  Granite       1959? 


2800         Sanders      ?? 


Forrester  1960,  1962: 

Rock  Creek  sheep 

range 

Baker  record  in  Pilsbry 

1939 


B-7 


Species 


Location 


TRS 


Elev  (ft)       County 


Date 


Habitat 


Notes^ 


Zacoleus 
idahoensis 


centered  on 
landing  site  at 
Wild  Horse 
Island,  Flathead 
Lake 


T24N,R20W, 
sec  13 


2900 


Lake 


1959? 


under  driftwood  near  Forrester  1960:  Wild 
shoreline  Horse  sheep  range 


^  ANSP  (Academy  of  Natural  Sciences,  Philadelphia),  CAS  (California  Academy  of  Sciences),  FMNH  (Field  Museum  of  Natural  History,  Chicago),  USNM  (U. 
S.  National  Museum). 


B-8 


APPENDIX  C.    GUIDELINES  FOR  DESIGNING  AND  CONDUCTING 
SURVEYS  OF  TERRESTRIAL  MOLLUSKS 


Survey  Guidelines  for  Terrestrial  MoUusks 

The  design  of  surveys  for  terrestrial  moUusks  is  fairly  simple  if  the  objective  is  to  look  specifically  for 
selected  target  species.  In  addition  to  determining  presence-absence,  some  additional  habitat 
information  can  be  collected  relatively  quickly  that  will  add  significantly  to  the  extremely  limited  body  of 
knowledge  on  the  ecology  of  most  species  of  conservation  concern  in  Montana.  With  this  in  mind,  the 
few  suggestions  that  follow  on  survey  methods  should  provide  biologists  unfamiliar  with  terrestrial 
moUusks  the  rudiments  needed  to  determine  presence-absence,  relative  abundance,  and  habitat 
associations  of  any  of  the  species  discussed  in  the  species  accounts  of  this  report.  Remember  that  with 
experience  comes  familiarity.  I  have  also  included  a  short  list  of  references  where  some  of  the 
techniques  are  discussed  in  more  detail  and  applied  to  particular  field  situations.  Frest  and  Johannes 
(1 995)  provide  a  summary  of  survey,  monitoring,  and  collection  methods.  New  (1 998)  provides  a 
broad  overview  on  survey  design  for  invertebrates  of  conservation  interest. 

Survey  Design 

The  target  species  of  conservation  interest  in  Montana  (Table  1)  can  be  readily  detected  through  labor- 
intensive  hand  searching.  Hand  searching  involves  picking  through  litter,  shallow  soil,  and  turning  over 
rocks  and  fallen  logs  looking  for  attached  animals.  The  length  of  time  spent  searching  is  recorded  to 
provide  a  relative  measure  of  search  effort  and  rate  of  encounter  (relative  abundance)  of  the  target 
species.  In  some  cases  it  may  be  desirable  to  do  searches  at  random  locations  along  transects  for 
quantitative  comparisons  by  habitat  or  site.  Search  areas  of  some  size  (e.g.  1x1  m)  are  examined  along 
transects  for  a  set  time,  and  the  number  of  individuals  found  in  each  search  plot  recorded. 

Habitat  data  associated  with  each  transect  and/or  plot  can  include  simple  things  such  as  estimates  of 
overhead  canopy  cover  and  species  composition,  the  same  for  ground  cover,  soil  type  or  source  rock 
type,  slope  and  exposure;  mean  particle  size  of  stones,  talus,  or  boulders  should  be  documented  at  sites 
in  rocky  terrain.  For  very  small  snails,  soil  samples  are  extracted  from  plots  and  screened  on  the  spot 
using  fine  sieves,  or  placed  in  bags  for  later  screening  either  through  sieves  or  under  Berlese  funnels; 
these  soil/litter  extraction  methods  are  not  especially  useful  for  the  species  discussed  in  this  report. 
Ambient  temperature,  cloud  cover,  comments  on  precipitation  (current,  recent,  and  duration)  and 
related  weather  data  should  be  recorded,  as  weather  is  a  significant  factor  in  determining  the  degree  of 
success  of  surveys.  For  recent  examples  of  how  sampling  can  be  tied  to  habitat  analyses  of  a  terrestrial 
moUusk  fauna,  see  Kralka  (1986)  and  Ports  (1 996).  A  broader  perspective  for  quantitative 
descriptions  of  moUusk  populations  and  habitats  is  presented  in  Bishop  (1 977). 

Use  of  cover  boards  provides  an  alternative  to  hand  searching,  and  is  also  useful  in  conjunction  with 
hand  searching.  Cover  boards  provide  quantitative  assessments  of  relative  abundance  that  are  suitable 
for  statistical  analyses,  and  they  also  are  useful  for  long-term  sampling  of  rare  species  at  specific 
locations  when  resources  for  field  surveys  are  limited  to  only  a  few  (or  no)  periods  of  hand  searching. 
However,  the  cover  board  technique  still  needs  assessment  in  talus  sites  to  determine  its  usefulness  in 
that  kind  of  substrate. 

At  selected  sites,  either  transects  or  grids  of  cardboard  or  masonite  squares  (transects  of  30  x  30  cm 
masonite  [Boag  1982];  selected  sites  with  56  x  71  cm  cardboard  [Gleich  and  Gilbert  1976];  grids  of  75 
X  75  cm  cardboard  [Stray er  et  al.  1 986])  are  placed  apart  at  regular  distances,  often  in  a  variety  of 

C-1 


habitats  or  microhabitats  in  comparative  studies.  Each  cover  board  represents  a  sample  plot  that  can  be 
checked  as  frequently  or  infrequently  as  resources  (money  and  personnel)  allow.  The  ground  where 
boards  are  placed  can  first  be  wetted  to  elevate  humidity  beneath  the  boards  (useful  for  revisits  of  only  a 
few  days  apart),  but  for  long-term  sampling  with  few  visits  it  is  probably  preferable  to  place  boards 
early  in  the  field  season  (spring,  once  ground  is  snow-free)  and  retrieve  them  in  mid  to  late  fall  before 
snow  again  covers  the  ground  (or  left  in  place  over  winter  and  revisited  the  following  spring).  Multiple 
visits  to  check  snails  and  slugs  under  the  boards  can  be  made  during  a  field  season;  visits  should  be 
made  to  all  transects  or  grids  at  regular  sampling  periods  (e.g.,  monthly,  bi-monthly,  annually). 

Vouchers  of  target  species  should  be  collected  to  confirm  identification.  Dead  shells  can  be  placed  in 
film  containers  and  protected  with  cotton.  Live  snails  and  slugs  can  be  kept  in  containers  with  moist 
paper  towels  or  wood  until  a  determination  can  be  made.  If  preservation  is  necessary,  snails  and  slugs 
should  be  drowned  in  warm  water,  fixed  in  formalin,  and  stored  in  vials  of  70%  ethyl  alcohol.  All 
collected  material  should  be  accompanied  by  the  date  and  location  of  collection. 

Timing  of  Surveys 

Terrestrial  moUusks  are  most  active  when  conditions  are  cool  and  wet.  During  warm  and  dry 
conditions,  a  site  may  be  searched  with  few  or  no  encounters,  when  under  moist  and  cool  conditions  the 
same  site  may  reveal  an  abundance  of  live  animals.  Of  course,  dead  shells  may  be  found  regardless  of 
the  weather,  but  finding  extant  populations  is  a  first  priority,  and  finding  slugs  will  require  favorable 
conditions  if  hand  collecting  is  conducted.  All  species  may  be  active  shortly  after  the  ground  becomes 
snow-free,  when  the  ground  is  moist  from  snowmelt,  and  will  remain  active  until  snow  covers  the  ground 
or  hard  freezes  occur,  except  during  periods  of  hot  dry  summer  weather.  For  Montana,  the  field  season 
extends  from  late  March  or  early  April  through  October  in  most  years  and  at  lower-elevation  sites. 

Some  searching  at  night  may  be  fruitful  during  drier  periods,  but  this  is  yet  to  be  determined  for  the 
species  discussed  in  this  report.  Brunson  (1 956)  speculated  that  the  Mission  Range  Disc  {Discus 
brunsoni)  could  be  most  active  in  talus  at  night,  when  moisture  conditions  are  more  favorable,  and  that 
might  explain  how  it  was  overlooked  for  so  many  years  at  the  same  locality  where  the  Carinate 
Mountainsnail  (Oreohelix  elrodi)  was  collected  frequently.  Talus-inhabiting  species  (all  species,  for  that 
matter)  could  show  heightened  surface  activity  at  night  when  humidity  levels  are  probably  elevated.  This 
possibility  is  worth  investigating,  as  it  has  implications  for  future  survey  protocols  for  terrestrial  moUusk 
species  of  conservation  concern  in  Montana. 

Literature  Cited 

Bishop,  M.  J.  1 977.  Approaches  to  the  quantitative  description  of  terrestrial  moUusk  populations  and 
habitats.  Malacologia  16:61-66. 

Boag,D.A.  1982.  Overcoming  sampling  bias  in  studies  of  terrestrial  gastropods.  Canadian  Journal  of 
Zoology  60:1289-1292. 

Brunson,R.B.  1956.  The  mystery  of  Discus  brunsoni.  The  Nautilus  70:16-21. 


C-2 


Frest,  T.  J.,  and  E.  J.  Johannes.  1 995.  Interior  Columbia  Basin  moUusk  species  of  special  concern. 
Final  Report  to  Interior  Columbia  Basin  Ecosystem  Management  Project.  Deixis  Consultants, 
Seattle.  274  pp. 

Gleich  J.  G,  and  F.  F.  Gilbert.  1 976.  A  survey  of  terrestrial  gastropods  from  central  Maine.  Canadian 
Journal  of  Zoology  54:620-627. 

Kralka,  R.  A.  1 986.  Population  characteristics  of  terrestrial  gastropods  in  boreal  forest  habitats. 
American  Midland  Naturalist  1 1 5 : 1 56- 1 64. 

New,T.  R.  1998.  Invertebrate  surveys  for  conservation.  Oxford  University  Press.  Oxford,  UK.  240 
pp. 

Ports,  M.  A.  1 996.  Habitat  affinities  and  distributions  of  land  gastropods  from  the  Ruby  Mountains 
and  East  Humboldt  Range  of  northeastern  Nevada.  The  Vehger  39:335-341 . 

Strayer,  D.,  D.  H.  Pletscher,  S.  P  Hamburg,  and  S.  C.  Nodvin.  1986.  The  effects  of  forest 

disturbance  on  land  gastropod  communities  in  northern  New  England.  Canadian  Journal  of 
Zoology  64:2094-2098. 


C-3 


APPENDIX  D.   KEY  TO  THE  GENERA  OF  TERRESTRIAL  MOLLUSKS 

OF  MONTANA 


Ml 


(undir  marrltil      |      lunbsi  martJt) 


WunWs  defl- 


Figure  D.l  Anatomy  of  a  Slug 


The  following  dichotomous  key  to  the  genera  of  terrestrial  moUusks  (slugs  and  snails)  in  Montana  is 
based  on  one  developed  and  revised  in  1 967  by  Dr.  Royal  Bruce  Brunson,  Lee  Fairbanks,  and  Richard 
Russell.  Excluded  in  this  current  version  are  all  aquatic  taxa.  The  key  is  presented  here  to  land 
managers  and  biologists  as  an  aid  in  identifying  slugs  and  snails  that  may  be  of  special  conservation 
concern.  In  the  case  of  slugs,  all  genera  of  special  interest  are  monotypic  (represented  by  a  single 
species)  in  Montana. 

All  Terrestrial  MoUusks 

1  a.  Shell  absent  externally  or  greatly  reduced  (go  to  slug  key), 
lb.  Shell  present,  covering  the  entire  animal  (go  to  snail  key). 

Slugs 

1  a.  Mantle  elevated  as  a  hump,  shell  may  be  partly  exposed  in  a  dorsal  slit  in  the  mantle — Hemphillia 
lb.  Mantle  not  elevated,  shell  never  exposed — 2 

2a.  Length  of  mantle  greater  than  two-thirds  the  length  of  the  animal — Magnipelta 
2b.  Length  of  mantle  less  than  two-thirds  the  length  of  the  animal — 3 

3a.  Sole  tripartite  (having  2  longitudinal  furrows),  back  generally  keeled  near  posterior  end, 

pneumostome  (breathing  pore)  in  posterior  half  of  mantle  margin — 4 

3b.  Sole  undivided,  back  not  keeled,  pneumostome  in  anterior  half  of  the  mantle  margin — 7 

4a.  Posterior  margin  of  mantle  notched,  pneumostome  above  or  in  front  (anterior)  of  mantle  cleft — 5 
4b.  Posterior  margin  of  mantle  unbroken,  pneumostome  behind  (posterior)  mantle  cleft — 6 

5a.  Color  black  or  dark  brown — Zacoleus 

5b.  Base  color  bluish-gray,  dark  lateral  lines  on  mantle — Udosarx 

6a.  Greater  than  50  mm  in  length,  base  color  tan,  variously  spotted  with  black — Umax 
6b.  Less  than  50  mm  in  length,  color  brown  or  black — Deroceras 

Idi.  Base  color  orange,  color  of  sole  much  the  same  as  upper  (dorsal)  surface,  anterior  third  of  mantle 
free  (unattached  to  dorsum),  caudal  pit  at  tip  of  tail  indistinct,  length  up  to  70  mm — Prophysaon 
7b.  Base  color  gray  or  orange  to  brown,  sole  generally  much  paler  than  upper  (dorsal)  surface,  caudal 
pit  at  tip  of  tail  distinct,  length  varies,  up  to  1 50  mm — Arion 


D-1 


Haklfann 


Pt^irlDrm 


LyiiinapTomi 


EkimtGr 


Figure  D.2  Some  shell  shapes. 


he^t 


paflB'iBl  ihHtn 


basal  loDth 


Figure  D.3  Shell  terminology,  (a):  striate  (indented  spiral  lines,  (b):  lirae  (raised  spiral  lines),  (c):  ribs 
(raised  transverse  lines),  (d):  wrinkles. 


Snails 

1  a.  Shell  lymnaeform  (elongated  coiled  spire  that  is  sharply  pointed) — 1 
lb.  Shell  not  lymnaeform — 4 

2a.  Body  whorl  greatly  enlarged,  spire  relatively  short;  shell  generally  thin  and  transparent — Oxyloma 
2b.  Body  whorl  not  greatly  enlarged  or  only  slightly  enlarged;  length  of  spire  at  least  a  third  the  length  of 
the  shell— 3 

3a.  Aperture  (opening  of  shell)  round;  shell  yellowish,  clear;  shell  surface  smooth  or  with  nothing  more 

than  fine  striae — Succinea 

3b.  Aperture  oval;  shell  often  chalky;  surface  with  very  fine  file-like  markings — Catinella 

4a.  Shell  heliciform  (fiattened  coil,  wider  than  tall) — 5 

4b.  Shell  pupiform  (elongated  coiled  spire,  taller  than  wide,  with  blunt  or  rounded  apex) — ^23 

5a.  Adult  shell  with  reflected  lip  at  aperture — 6 
5b.  Adult  shell  without  reflected  lip — 8 

6a.  Aperture  with  teeth — Triodopsis  (Cryptomastix) 
6b.  Aperture  without  teeth — 7 

7a.  Size  2-3  mm — Vallonia 
7b.  Size  to  20  mm — Allogona 

8a.  Shell  thin  and  transparent,  generally  smooth,  less  than  1 0  mm  in  diameter — 9 

8b.  Shell  opaque  or  with  a  color  pattern;  surface  generally  with  ridges  or  striae;  size  varies — 1 7 

9a.  Body  whorl  greatly  enlarged,  consisting  of  three  quarters  of  the  shell — Vitrina 
9b.  Body  whorl  not  greatly  enlarged  or  only  slightly  enlarged — 1 0 

1  Oa.  Widely  umbilicated,  width  of  umbilicus  (central  depression  on  the  undersurface  penetrating  into  the 
layered  coils)  one  third  or  more  the  width  of  the  shell — 1 1 
1  Ob.  Narrowly  umbilicated — 1 2 

11a.  Shell  less  than  2  mm  in  diameter;  3.0-3.5  whorls — Striatura 
1  lb.  Shell  2.5  mm  in  diameter;  4.0-5.0  whorls — Hawaiia 

12a.  Whorls  about  5,  tightly  coiled — 1 3 
12b.  Whorls  not  tightly  coiled — 15 

13a.  Shell  nearly  as  high  as  broad,  beehive-shaped — Euconulus 
1 3b.  Height  of  shell  little  more  than  half  of  the  diameter — 1 4 


D-2 


14a.  Umbilicus  closed;  less  than  5  whorls,  spire  somewhat  elevated — Pristiloma 
14b.  Umbilicus  open;  more  than  5  whorls;  spire  flat — Microphysula 

1 5a.  Shell  height  less  than  half  of  the  diameter;  more  than  5  whorls — Oxychilus 
1 5b.  Shell  height  greater  than  half  of  the  diameter;  less  than  5  whorls — 1 6 

1 6a.  Whorls  increasing  in  size,  the  body  whorl  being  quite  enlarged;  shell  clear  and  shiny — Retinella 
1 6b.  Whorls  much  the  same  size;  shell  amber  or  horn-colored,  cloudy — Zonitoides 

1 7a.  Composition  of  shell  chalky,  often  with  a  color  pattern  (banding)  or  various  ridges — Oreohelix 
1 7b.  Composition  of  shell  chitinous  or  homy;  color  yellow  or  brown — 1 8 

1 8a.  Diameter  of  shell  greater  than  1 5  mm;  whorls  5-6 — 1 9 
1 8b.  Diameter  of  shell  less  than  12  mm;  whorls  4-8 — 20 

1 9a.  Height  of  shell  greater  than  half  the  diameter;  size  1 7-25  mm — Anguispira 
1 9b.  Height  of  shell  less  than  half  the  diameter;  size  22-32  mm — Haplotrema 

20a.  Diameter  of  shell  less  than  2.5  mm — Punctum 
20b.  Diameter  of  shell  5-12  mm — 21 

21a.  Apical  1 .5  whorls  with  spiral  striations — Radiodiscus 
21b.  Apical  whorls  bare  or  with  radial  growth  lines — ^22 

22a.  Whorls  7-8,  tightly  coiled;  aperture  with  teeth — Polygyrella 
22b.  Whorls  4-5,  not  tightly  coiled;  aperture  without  teeth — Discus 

23  a.  Aperture  without  teeth — 24 
23b.  Aperture  with  teeth — 25 

24a.  Aperture  round;  shell  3  mm  in  height — Columella 
24b.  Aperture  ovate;  shell  5  mm  in  height — Cionella 

25a.  Six  whorls;  2-3  teeth  in  aperture — Pupilla 
25b.  Seven  whorls;  more  than  3  teeth  in  aperture — 26 

26a.  Three  teeth  in  the  aperture  on  parietal  (outer)  wall;  whorls  about  the  same  width — Vertigo 
26b.  Four  teeth  in  the  aperture  on  parietal  wall;  body  whorl  widest  of  the  whorls — Gastrocopta 


D-3