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A Stereo-Atlas  of  Ostracod  Shells 


edited  by  R.  H.  Bate,  D.  J.  Horne,  J.  W.  Neale, 

and  David  J.  Siveter 


Volume  14,  Part  1;  30th  May,  1987 


Published  by  the  British  Micropalaeontological  Society,  London 


Editors 


Dr  R.H.  Bate,  SSI  (UK)  Ltd.,  Tannery  House,  Tannery  Lane,  Send,  Woking,  Surrey  GU23  7EF. 
Dr  D.J.  Horne,  Department  of  Geology,  City  of  London  Polytechnic,  Walburgh  House,  Bigland  Street, 
London  El  2NG. 

Prof.  J.W.  Neale,  Department  of  Geology,  The  University,  Hull  HU6  7RH. 

Dr  David  J.  Siveter,  Department  of  Geology,  The  University,  Leicester  LEI  7RH. 


Editorial  Board 

Dr  G.  Bonaduce,  Stazione  Zoologica,  80121  Napoli,  Italy. 

Dr  J.-P.  Colin,  Esso  Production  Research  - European,  213  Cours  Victor  Hugo,  33321  Begles,  France. 
Dr  P.  De  Deckker,  Research  School  of  Pacific  Studies,  Australian  National  University,  PO  Box  4, 
Canberra  ACT  2600.  Australia. 

Dr  D.  van  Harten,  Universiteit  van  Amsterdam,  Geologisch  Instituut,  Nieuwe  Prinsengracht  130, 
Amsterdam.  The  Netherlands. 

Dr  I.  Purper,  Departamento  de  Paleontologia  e Estratigrafia,  UFRGS,  90  000  Porto  Alegre  RS,  Brazil. 
Dr  R.E.L.  Schallreuter,  Universitat  Hamburg,  Geologisch-Palaontologisches  Institut,  Bundesstrasse 
55,  D 2000  Hamburg  13,  West  Germany. 


Officers  of  the  British  Micropalaeontological  Society 

Chairman  Dr  A.C.  Higgins,  BP  Research  Centre,  Chertsey  Road,  Sunbury-on-Thames,  Middlesex 
TW16  7LN. 

Secretary  Dr  P.P.E.  Weaver,  Institute  of  Oceanographic  Sciences,  Brook  Road,  Wormley,  Godaiming, 
Surrey  GU8  5UB.  Tel:  0428-79  4141. 

Treasurer  Dr  J.E.  Whittaker,  Department  of  Palaeontology,  British  Museum  (Natural  History), 
Cromwell  Road,  London  SW7  5BD.  Tel:  01-589  6323. 

Journal  Editor  Dr.  L.M.  Sheppard,  SSI  (U.K.)  Limited,  Chancellor  Court,  20  Priestly  Road,  Guildford, 
Surrey  GU2  5YL.  Tel:  (0483)  506605. 

Newsletter  Editor  Dr  R.L.  Austin,  Department  of  Geology,  University  of  Southampton,  Southampton 
S09  5NH.  Tel:  (0703)  559122/557941 

Conodont  Group  Chairman  Dr  R.J.  Aldridge,  Department  of  Geology,  University  of  Nottingham, 
University  Park,  Nottingham  NG7  2RD. 

Secretary  Dr  P.M.  Smith,  Department  of  Earth  Sciences,  University  of  Cambridge,  Downing  Street, 
Cambridge  CB2  3EQ.  Tel:  (0223)  355463  (or  276121). 

Foraminifera  Group  Chairman  Dr  P.  Copestake,  Britoil,  150  St.  Vincent  Street,  Glasgow  G2  5LJ. 

Secretary  Dr  D.J.  Shipp,  Robertson  Research  Int.  Limited,  Ty’n-y-Coed,  Llanrhos,  Llandudno  LL30 
ISA.  Tel:  (0492)  81811. 

Microplankton  Group  Chairman  Dr  G.L.  Eaton,  BP  Research  Centre,  Chertsey  Road,  Sunbury-on- 
Thames,  Middlesex  TW16  7LN. 

Secretary  Dr  A.J.  Powell,  BP  Research  Centre,  Chertsey  Road,  Sunbury-on-Thames,  Middlesex  TW16 
7LN.  Tel:  (09327)  62818. 

Ostracod  Group  Chairman  Dr  D.J.  Horne,  Geology  Department,  City  of  London  Polytechnic, 
Walburgh  House,  Bigland  Street,  London  El  2NG. 

Secretary  Dr  C.  Maybury,  Department  of  Geology,  University  College  of  Wales,  Aberystwyth,  Dyfed 
SY23  3DB.  Tel:  (0970)  3111. 

Palynology  Group  Chairman  Dr  M.C.  Boulter,  N.E.  London  Polytechnic,  Romford  Road,  London  E15 
4LZ. 

Secretary  Dr  J.E. A.  Marshall,  Department  of  Geology,  The  University,  Southampton  S09  5NH.  Tel: 
(0703)  559122. 

Calcareous  Nannofossil  Group  Chairman  Mr  M.  Jakubowski,  Robertson  Research  Int.  Limited, 
Ty’n-y-Coed,  Llanrhos,  Llandudno,  Gwynedd  LL30  ISA. 

Secretary  Dr  J.  Crux,  BP  Research  Centre,  Chertsey  Road,  Sunbury  on  Thames,  Middlesex  TW16  7LN. 
Tel:  (09327)  63062. 


Instructions  to  Authors 

Contributions  illustrated  by  scanning  electron  micrographs  of  Ostracoda  in  stereo-pairs  are  invited. 
Format  should  follow  the  style  set  by  the  majority  of  papers  in  this  issue.  Descriptive  matter  apart  from 
illustrations  should  be  cut  to  a minimum;  preferably  each  plate  should  be  accompanied  by  one  page  of 
text  only.  Blanks  to  aid  in  mounting  figures  for  plates  may  be  obtained  from  any  one  of  the  Editors  or 
Editorial  Board.  Completed  papers  should  be  sent  to  Dr  David  J.  Siveter. 


The  front  cover  shows  a left  valve  of  Neolimnocy there  hexaceros  Delachaux,  1928,  from  Quaternary 
Deposits  at  Lago  Junin,  Peru.  Photograph  by  Dr  P.  De  Deckker,  University  of  Monash,  Victoria, 
Australia. 


Printed  in  the  UK  by  BPCC  Northern  Printers  Ltd.,  Stanley  Road,  Blackpool  FY1  4QN 


Stereo-Atlas  of  Ostracod  Shells  14  (1)  1-4(1987)  Cathaycythere  reticulata  ( 1 of  4) 

595.337.14  (119.4)  (265.72  : 161.108.21  + 161.109.21)  : 551.351  + 552.51  + 52 


ON  CATHAYCYTHERE  RETICULATA  WHATLEY  & ZHAO  gen.  et  sp.  nov 

by  Robin  Whatley  & Zhao  Quanhong 

(University  College  of  Wales,  Aberystwyth,  UK  & Tongji  University,  Shanghai,  China) 


Derivation  of  name: 

Genus  CATHAYCYTHERE  gen.  nov. 

Type-species:  Cathaycythere  reticulata  gen.  et  sp.  nov. 

From  Cathay  (China)  + cythere;  with  reference  to  the  type  locality  of  the  type-species  in  the  South 
China  Sea. 

Diagnosis: 

Medium  sized;  subrectangular  in  lateral  view,  highest  anterodorsally  and  longest  subventrally; 
anterior  margin  broadly  rounded;  posterior  margin  truncate  above  and  bluntly  pointed  below. 
Carapace  laterally  compressed  at  both  end  margins.  Eye-tubercle  and  internal  ocular  sinus  absent. 
Surface  coarsely  and  irregularly  reticulate  with  a prominent  subcentral  node  surrounded  by  a 
subcircular  sulcus.  Hinge  holamphidont  with  high  conical  anterior  tooth,  bulbous  posterior  tooth 
and  locellate  median  element  in  right  valve.  Inner  lamella  wide  with  a marked  oval  excavation 
posteriorly  aligned  parallel  to  the  postero-dorsal  slope  of  the  posterior  margin;  very  narrow 
vestibulae  at  each  end;  radial  pore  canals  few,  long,  thin  and  simple.  Adductor  scars  relatively 
small,  consisting  of  a vertical  row  of  four;  frontal  scar  single,  oval. 

Explanation  of  Plate  14,  2 

Fig.  1,  RV,  ext.  lat.  (holotype,  1986.404,  710/xm  long);  fig.  2,  LV,  ext.  lat.  (paratype,  1986.405,  665/xm  long);  fig.  3,  LV,  ext.  lat. 

(paratype,  1986.406,  665/xm  long). 

Scale  A (100/xm;  x90),  figs.  1-3. 

Stereo-Atlas  of  Ostracod  Shells  14,  3 Cathaycythere  reticulata  (3  of  4) 


Remarks: 

The  excavation  on  the  wide  posterior  inner  lamella  is  not  known  to  occur  in  any  other  genus  and 
can  be  used  to  distinguish  it  from  Sinocythere  Hou,  1978.  The  latter  is  closest  in  ornament  and 
muscle  scar  pattern  to  the  present  genus,  but  differs  in  hingement  (hemiamphidont  with  clearly 
crenulate  posterior  tooth)  and  in  lacking  the  posterior  excavation  on  the  inner  lamella.  Kritlie 
exhibits  a similar  excavation  posteriorly  but  it  occurs  distal  to  the  selvage  whereas  in  Cathaycythere 
it  is  proximal.  The  familial  status  of  Cathaycythere  is  uncertain  and  possibly  a new  family  is 
required  to  accommodate  this  genus  and  Sinocxthere  (see  Whatlev  & Zhao,  Stereo-Atlas  Ostracod 
Shells  14,  5-8,  1987). 

Cathaycythere  reticulata  Whatley  & Zhao  gen.  et  sp.  nov. 

Holotype: 

British  Museum  (Nat.  Hist.)  no.  1986.404;  RV. 

Type  locality: 

[Paratypes:  British  Museum  (Nat.  Hist.)  nos.  1986.405-409.) 

Off  Guangsi  Province  of  China,  Gulf  of  Tonkin,  South  China  Sea;  lat.  21°  29'  09"N,  long.  108°  44' 
46"E.  Recent,  water  depth;  14m. 

Derivation  of  name: 
Figured  specimens: 

With  reference  to  its  reticulate  surface. 

British  Museum  (Nat.  Hist.)  nos.  1986.404  (holotype,  RV;  PI.  14,  2,  fig.  1),  1986.405  (paratype, 
LV:  PI.  14,  2,  fig.  2),  1986.406  (paratvpe,  LV:  PI.  14,  2,  fig.  3),  1986.407  (paratvpe,  car.:  PI.  14.  4, 
fig.  1),  1986.408  (paratype.  LV:  PI.  14,  4,  fig.  2),  1986.409  (paratype,  RV:  PI.  14,  4,  fig.  3).  Nos. 
1986.404-406  are  from  the  type  locality.  Nos.  1986.407-409  are  from  lat.  21°  15'  46"N,  long.  109° 
24'  57"E;  Recent,  water  depth:  14m. 

Diagnosis: 

Distribution: 

As  for  the  genus.  Monotypic. 

In  four  bottom  samples  off  Guangsi  Province,  China,  northern  Gulf  of  Tonkin,  South  China  Sea. 
Water  depth:  10  - 16m;  substrate:  mud  to  fine  sand. 

Explanation  of  Plate  14,  4 

Fig.  1,  car.,  ext.  dors,  (paratype,  1986.407,  635/xm  long);  fig.  2,  LV,  int.  lat.  (paratype,  1986.408,  635/xm  long);  fig.  3,  RV,  int.  lat 
(paratype,  1986.409,  645/xm  long). 

Scale  A (100/xm;  x90),  figs.  1-3. 


Cathaycythere  reticulata  (2  of  4) 


Stereo-Atlas  of  Ostracod  Shells  14,  2 


Stereo-Atlas  of  Ostracod  Shells  14,  4 


Cathaycythere  reticulata  (4  of  4) 


Stereo-Atlas  of  Ostracod  Shells  14  (2)  5-8  (1987)  Sinocy there  sinensis  (1  of  4) 

595.337.14  (119.9)  (510  : 161.120.34)  : 551.351 

ON  SINOCYTHERE  SINENSIS  HOU 

by  Robin  Whatley  & Zhao  Quanhong 

(University  College  of  Wales,  Aberystwyth,  UK  & Tongji  University,  Shanghai,  China) 

Genus  SINOCYTHERE  Hou,  1982 
Type-species  (by  original  designation):  Sinocythere  sinensis  Hou,  1982 
Diagnosis:  Medium  sized;  subrectangular  in  lateral  view  with  parallel  dorsal  and  ventral  margins,  prominent 

posterior  cardinal  angle  and  obtusely  rounded  posterior  margin.  Eye-tubercle  weakly  developed 
but  internal  ocular  sinus  not  developed.  Surface  reticulate  with  an  anteromedian  node  surrounded 
by  a subcircular  sulcus.  Hinge  hemiamphidont:  anterior  tooth  in  right  valve  conical,  posterior 
tooth  curved  and  distinctly  dentate;  in  left  valve,  anterior  socket  enclosed  ventrally  by  an  anterior 
extension  of  the  anteromedian  conical  tooth,  posterior  socket  with  an  anti-slip  toothlet 
ventromedianly,  and  median  bar  denticulate.  Inner  lamella  relatively  wide  with  shallow  anterior 
vestibule;  radial  pore  canals  few,  thin  and  simple.  Adductor  muscle  scars  small,  consisting  of  a 
vertical  row  of  four  scars  all  in  contact;  frontal  scar  single,  oval. 

Remarks:  This  genus  is  close  to  Spinoleberis  Hanai,  1961  in  many  features  except  that  the  latter  has  a 
triangular  outline  and  much  narrower,  more  acute  posterior  margin  in  lateral  view,  and  three 
longitudinal  ribs.  In  external  characters  Sinocythere  is  somewhat  similar  to  Palmenella  Hirschman, 
1916,  but  the  latter  bears  a schizodont  hinge.  Cathaycythere  Whatley  & Zhao,  1987  ( Stereo-Atlas 
Ostracod  Shells  14,  1-4)  has  similar  ornament  and  also  the  circular  sulcus  surrounding  the 
anteromedian  node.  The  two  genera  differ  in  hingement  and  Sinocythere  lacks  the  excavated 
posterior  inner  lamella  so  typical  of  Cathaycythere.  Sinocythere  and  Cathaycythere  are  probably 
worth  including  in  a new  family  of  Cytheracea. 


Explanation  of  Plate  14,  6 

Fig.  1,  cf  RV,  ext.  lat.  (1986.410,  570/u.m  long);  fig.  2,  § car.,  rt.  lat.  (1986.411.  540/u.m  long);  fig.  3,  9 car..  It.  lat.  (1986.411,  540/u.m 
long).  Scale  A (100/u.m;  xllO),  figs.  1-3. 


Stereo-Atlas  of  Ostracod  Shells  14,  7 


Sinocythere  sinensis  (3  of  4) 


Sinocythere  sinensis  Hou,  1982 


1982  Sinocythere  sinensis  sp.  nov.  Hou  in  Hou  et  al.,  Cretaceous-Quaternary  ostracode  fauna  from  Jiangsu,  242,  text-fig.  77;  pi.  87, 
figs.  16-19. 

1985  Sinocythere  sinensis  Hou;  Zhao,  Acta  Oceanologica  Sinica,  pi.  2,  fig.  10. 

1985  Sinocythere  sinensis  Hou;  Wang  and  Zhao,  in  Wang  et  al.,  Marine  Micropaleontology  of  China,  pi.  18,  fig.  4. 


Holotype: 
Type  locality: 
Figured  specimens: 


Diagnosis: 


Remarks: 

Distribution: 


Nanjing  Institute  Geology  & Paleontology,  Academia  Sinica;  no.  4107.  9 LV.  Not  figured  herein. 
Jiangsu  Province,  Eastern  China;  Dongtai  Formation,  Quaternary. 

British  Museum  (Nat.  Hist.)  nos.  1986.410  (cf  RV:  PI.  14.  6,  fig.  1;  PI.  14.  8,  fig.  3).  1986.411  (9 
car.:  PI.  14,  6,  figs.  2,  3;  PI.  14,  8,  fig.  1),  1986.412  (9  LV:  PI.  14,  8,  fig.  2).  All  Recent,  collected 
from  the  littoral  of  Jiangsu  Province,  China;  approx,  lat.  34°  17'N,  long.  120°  17'E. 
Irregularly  polygonal  surface  reticulation  with  superimposed  narrow,  oblique  posterodorsal- 
anteroventral  rib,  and  a bifid  rib  running  from  the  anterior  cardinal  angle  obliquely  to 
mid-anterior.  Female  carapace  strongly  laterally  compressed  posterodorsally.  posteriorly  and 
ventrally;  the  male  is  inflated  in  these  areas. 

This  species  is  very  close  to  S.  dongtaiensis  Chen,  1982  in  outline  and  overall  ornamentation,  but 
the  latter  is  much  more  weakly  reticulate. 

Pliocene  to  Recent,  Eastern  China.  Recent  specimens  most  abundant  in  littoral  zone  and  inner 
shelf  shallower  than  20m,  rare  in  estuaries  and  water  depths  from  20  to  200m. 


Explanation  of  Plate  14,  8 

Fig.  1,  9 car.,  ext-  dors.  (1986.411,  540jum  long);  fig.  2,  9 LV,  int.  lat.  (1986.412,  490/xm  long);  fig.  3,  cf  RV,  int.  lat.  (1986.410, 
570/u.m  long). 

Scale  A (100/u.m;  xllO),  figs.  1-3. 


Stereo- Atlas  of  Ostracod  Shells  14,  6 


Sinocythere  sinensis  (2  of  4) 


Stereo-Atlas  of  Ostracod  Shells  14,  8 


Sinocythere  sinensis  (4  of  4) 


Stereo-Atlas  of  Ostracod  Shells  14  (3)  9-12  (1987)  Albileberis  sinensis  (1  of  4) 

595.337.14  (119)  (510  : 161.120.34)  : 551.313.1  + 551.35 

ON  ALBILEBERIS  SINENSIS  HOU 

by  Zhao  Quanhong  & Robin  Whatley 

(Tongji  University,  Shanghai , China  & University  College  of  Wales,  Aberystwyth,  UK) 

Genus  ALBILEBERIS  Hou,  1982 
Type-species:  Albileberis  sinensis  Hou,  1982 

Diagnosis:  Small  to  medium,  laterally  compressed;  subovate  to  rectangular  in  lateral  view  with  greatest  height 

anteromedianly.  Bluntly  truncate  posterior  and  well  rounded  anterior  margins.  Surface  smooth, 
pitted  or  reticulate.  Hinge  between  paleomerodont  and  holomerodont;  all  positive  elements  in 
right  valve,  long  ridge-like  anterior  tooth  thickened  anteriorly  with  a prominent  square  terminal 
toothlet,  median  bar  smooth  anteriorly  and  faintly  crenulate  posteriorly,  posterior  tooth  curved 
and  denticulate.  Complementary  negative  elements  in  left  valve  with  an  anti-slip  bar  below  median 
groove  and  anterior  socket,  and  two  small  terminal  anti-slip  toothlets  respectively  at  anterior  and 
posterior  ends.  Inner  lamella  moderately  wide  with  large  vestibulae  and  narrow  fused  zone;  radial 
pore  canals  moderate  in  number  and  simple.  Adductor  muscle  scars  a vertical  row  of  four;  frontal 
scar  V-shaped;  fulcral  point  crescentic  and  prominent. 

Remarks:  Although  the  generic  name  Albileberis  was  first  published  in  Guan  et  al.  ( Paleontological  Atlas  of 

Central  & S China  (4):  Ostracoda,  1978),  who  attributed  the  genus  to  Hou  from  an  earlier  MS 
name,  its  type-species  was  not  published  until  1982  (Hou  in  Hou  et  al.).  This  genus  is  easily 
identified  by  its  laterally  compressed  carapace,  outline  and  peculiar  hingement,  and  probably 
belongs  to  the  Cytherideinae  based  on  its  internal  characters. 


Explanation  of  Plate  14,  10 

Fig.  1,  $ RV,  ext.  lat.  (1986.413,  525/u.m  long);  fig.  2,  9 LV,  ext.  lat.  (1986.414.  525pm  long);  fig.  3,  cf  LV.  ext.  lat.  ( 1986.415.  495/im 
long). 

Scale  A (lOO/um;  xl20),  figs.  1-3. 


Stereo-Atlas  of  Ostracod  Shells  14,  1 1 Albileberis  sinensis  (3  of  4) 

Albileberis  sinensis  Hou,  1982 


1982  Albileberis  sinensis  sp.  nov.  Hou,  in  Hou  et  al. , Cretaceous-Quaternary  ostracode  fauna  from  Jiangsu.,  240-241,  text-fig.  75.  pi. 
88,  figs.  1-7. 

1985  Albileberis  sinensis  Hou;  Zhao,  Acta  Oceanological  Sinica,  pi.  1,  fig.  9. 

1985  Albileberis  sinensis  Hou;  Wang  & Zhao,  in  Wang  et  al.,  Marine  Micropaleontology  of  China,  pi.  7,  fig.  2,  text-fig.  5. 


Holotype: 

Type  locality: 
Figured  specimens: 

Diagnosis: 

Remarks: 

Distribution: 


Nanjing  Institute  Geology  & Paleontology,  Academia  Sinica;  no.  41062;  9 LV.  Not  figured 
herein. 

Jiangsu  Province,  E China;  Dongtai  Formation,  Quaternary. 

British  Museum  (Nat.  Hist.)  nos.  1986.413  (9  RV:  PI.  14,  10,  fig.  1),  1986.414  (9  LV:  PI.  14,  10, 
fig.  2),  1986.415  (cf  LV:  PI.  14,  10,  fig.  3),  1986.416  (9  car.:  PI.  14,  12,  fig.  1),  1986.417  (9  LV:  PI. 
14,  12,  fig.  2),  1986.418  (9  RV:  PI.  14,  12,  fig.  3).  All  Recent,  collected  from  the  littoral  of  Jiangsu 
Province,  China;  approx,  lat.  34°  17'N,  long.  120°  17'E. 

Subovate  in  lateral  view  with  vertical  truncated  posterior  margin,  surface  smooth  with  few  very 
weak  reticulae  around  the  margins. 

Markedly  differs  from  the  other  two  species  in  this  genus.  A.  sheyangensis  Chen,  1982  is  much 
more  elongate  and  lower  with  obliquely  truncated  posterior  margin,  and  A.  asperata  Guan,  1978 
has  an  ornamentation  of  coarse  reticulation. 

China,  Quaternary  to  Recent.  At  the  present  day  this  species  is  abundant  and  widespread  in 
brackish  and  nearshore  waters  along  the  coast  of  the  East  China  and  Yellow  Seas  with  a salinity 
range  of  3%o  to  normal  sea  water,  including  marshes,  estuaries,  littoral  and  the  inner  shelf 
shallower  than  50m. 


Explanation  of  Plate  14,  12 

Fig.  1,  9 car.,  ext.  dors.  (1986.416,  535,u,m  long);  fig.  2,  9 LV,  int.  lat.  (1986.417,  515pm  long);  fig.  3,  9 RV.  int . lat.  (1986.418. 
515jU,m  long). 

Scale  A (lOOpun;  xl20),  figs.  1-3. 


Stereo-Atlas  of  Ostracod  Shells  14,  10 


Albileberis  sinensis  (2  of  4) 


Stereo-Atlas  of  Ostracod  Shells  14,  12 


Albileberis  sinensis  (4  of  4) 


Stereo-Atlas  of  Ostracod  Shells  14  (4)  13-16  (1987)  Sinocytheridea  impressa  (1  of  4) 

595.337.14  (118.22  + 119.9)  (512.317  + 510  : 161.118.39)  : 551.313.1  + 551.35 


ON  SINOCYTHERIDEA  IMPRESSA  (BRADY) 

by  Zhao  Quanhong  & Robin  Whatley 

(Tongji  University,  Shanghai,  China  & University  College  of  Wales,  Aberystwyth,  UK) 


Genus  SINOCYTHERIDEA  Hou,  1978 
Type-species  (by  subsequent  designation)  : S.  latiovata  Hou  & Chen,  1982 
(=  Cytheridea  impressa  Brady,  1869;  see  below) 

Diagnosis:  A genus  of  Cytherideidae  characterized  by  its  modified  antimerodont  hingement  with  a 

conspicuous  anti-slip  toothlet  anteriorly  in  the  left  valve,  by  which  it  can  be  readily  distinguished 
from  such  similar  genera  as  Cyprideis  Jones,  1857,  Neocyprideis  Apostolescu,  1965  and 
Sarsicytheridea  Athersuch,  1982. 

Remarks:  Sinocytheridea  was  named  by  Hou  in  manuscript  more  than  20  years  ago  but  remained 

unpublished  until  Guan  et  al.  (1978)  first  applied  this  name  for  the  genus  in  a published  work, 
attributing  the  genus  to  Hou  and  using  Hou's  original  description.  5.  latiovata  Hou  & Chen,  1982 
was  designated  by  Hou  and  Chen  in  Hou  et  al.  (1982)  as  the  type-species  of  Sinocytheridea.  The 
present  authors,  however,  have  recently  studied  Brady’s  material  from  Hong  Kong  which  is 
deposited  in  the  Hancock  Museum  and  consider  5.  latiovata  and  Cytheridea  impressa  Brady,  1869 
to  be  conspecific.  We  therefore  consider  C.  impressa  to  be  the  type-species  of  Sinocytheridea. 


Explanation  of  Plate  14,  14 

Figs.  1,  $ car.,  rt.  ext.  lat  (paralectotype,  1.23.44,  740  pm  long);  fig.  2,  9 LV.  ext.  lat.  (1986.419,  720  pm  long);  fig.  3,  9 car.,  ext- 
dors.  (1986.421,  750  pm  long). 

Scale  A (100  p.m;  x 85),  figs.  1-3. 


Stereo- Atlas  of  Ostracod  Shells  14,  15  Sinocytheridea  impressa  (3  of  4) 

Sinocytheridea  impressa  (Brady,  1869) 

1869  Cytheridea  impressa  sp.  nov.  G.S.  Brady  in  L.  De  Folin  and  L.  Perier  (eds.).  Les  Fonds  de  la  Mer.,  158,  pi.  16,  figs.  13,  14. 
1978  Cyprideis  yehi  Hu  & Yeh,  Geol.  Soc.,  China  (Taiwan),  Proc.,  21,  157-159,  text-fig.  5,  pi.  3.  figs.  10-13. 

1978  Sinocytheridea  sinensis  Hou;  Hou  in  Guan  et  al.,  Paleontological  Atlas  Central  & S China  (4):  Ostracoda,  240,  pi.  65,  figs.  1-5. 

1982  Sinocytheridea  latiovata  sp.  nov.  Hou  & Chen  in  Hou  et  al.,  Cretaceous-Quaternary  ostracode  fauna  from  Jiangsu,  164-165, 
text-figs.  26a-c,  pi.  72,  figs.  10-20. 

Sinocytheridea  longa  Hou  & Chen,  ibid.  165-166,  text-figs.  27a-c,  pi.  72,  figs.  T9. 


1982 


Lectotype: 


Type  locality: 
Figured  specimens: 


14,  16,  fig. 
14,  14,  fig. 


Hancock  Museum,  Newcastle-upon-Tyne,  England,  no.  1.24.37,  9 LV. 

[Paralectotypes:  Hancock  Mus.,  nos.  1.24.38,  9 RV;  1.23.44,  9 car.] 

Hong  Kong  Harbour;  Recent. 

Hancock  Museum,  Newcastle-upon-Tyne,  England,  nos.  1.24.37  (lectotype,  9 LV:  PI. 

2) ,  1.24.38  (paralectotvpe.  9 RV:  PI.  14,  16,  fig.  3),  1.23.44  (paralectotvpe,  9 car.;  PI. 

1),  Brit.  Mus.  (Nat.  Hist.)  nos.  1986.419  (9  LV:  PI.  14,  14,  fig.  2).  1986.421  ($  car.:  PI.  14.  14.  fig. 

3) ,  1986.420  (cf  LV:  PI.  14,  16,  fig.  1).  Nos.  1.23.44,  1.24.37  and  1.24.38  belong  to  the  Brady 
Collection  in  the  Hancock  Museum  and  are  from  the  type-locality;  nos.  1986.419-431  are  from  the 
Pohai  Bya,  China,  lat.  39°  50'N,  long.  118°  46'E,  water  depth:  15m. 

Elongate-oval  without  obvious  trace  of  angle  in  lateral  view'.  RV  larger  than  and  slightly 
overlapping  LV  along  the  periphery  except  anterior  margin.  Surface  smooth  with  rounded  shallow' 
pits  (openings  of  sieve-type  normal  pore  canals).  Avestibulate,  radial  pore  canals  few,  simple. 
Adductor  muscle  scar  a vertical  row  of  four  elongate  scars;  frontal  scar  V-shaped. 

Apart  from  the  more  elongate  outline,  5.  longa  Hou  & Chen  is  identical  in  carapace  features  to  S. 
impressa.  The  authors  believe  that  the  former  species  is  based  on  males  of  S.  impressa. 
Pliocene  to  Recent,  China.  The  modern  representatives  occur  widely  in  shelf,  littoral,  estuaries, 
marshes,  tidal  pools  and  channels  of  the  supralittoral  zone  along  the  entire  coast  of  China  w'ith  a 
salinity  distribution  ranging  from  about  2%o  to  normal  sea  water  and  a w'ater  depth  ranging  from 
middle  shelf  (50-f00m)  to  supralittoral. 

Explanation  of  Plate  14,  16 

Fig.  1,  cf  LV,  ext.  lat.  (1986.420,  660  pm  long);  fig.  2,  9 LV,  int.  lat.  (lectotype,  1.24.37,  775  pm  long);  fig.  3,  9 RV.  int.  lat. 
(paralectotype,  1.24.38,  740  yum  long).  Scale  A (100  /im;  x 85),  figs.  1-3. 


Diagnosis: 


Remarks: 


Distribution: 


Stereo- Atlas  of  Ostracod  Shells  14,  16 


Sinocytheridea  impressa  (4  of  4) 


Stereo- Atlas  of  Ostracod  Shells  14,  14 


Sinocytheridea  impressa  (2  of  4) 


Stereo-Atlas  of  Ostracod  Shells  14  (5)  17-20  (1987) 

595.337. 14  (118.22)  (798  : 162.153.70)  : 551.351  + 552.52 


Pterygocythereis  vannieuwenhuisei  (1  of  4) 


ON  PTERYGOCYTHEREIS  VANNIEUWENHUISEI  BROUWERS  sp.  nov. 

by  Elisabeth  M.  Brouwers 
(U.S.  Geological  Survey,  Denver) 


1986  Pterygocythereis 
Holotype: 

Type  locality: 


Derivation  of  name: 
Figured  specimens: 


Diagnosis: 


sp 
U.S 


nov. 


Pterygocythereis  vannieuwenhuisei  sp.  nov. 

C.  A.  Repenning,  E.  M.  Brouwers,  et  al.,  Bull.  U.S.  Geol.  Surv.,  1687,  pi.  1,  fig.  1. 
National  Museum  no.  410130,  cf  RV. 

[Paratypes:  U.S.  National  Museum  nos.  410131-410134]. 

Cutbank  on  a tributary  of  the  Kalikpik  River,  Arctic  coastal  plain.  North  Slope,  Alaska  (lat.  70° 
26.7'N,  long.  152°  09.4'W);  Pliocene.  Outcrop  consists  of  1.8m  of  late  Pliocene  marine  clay  and 
sand  overlain  by  5.5m  of  Pleistocene  fluvial  and  eolian  sands.  Deeper  inner  sublittoral  to  middle 
sublittoral  water  depths;  cold  temperate  to  subfrigid  marine  climate. 

In  honour  of  Don  Van  Nieuwenhuise,  research  geologist  at  Amoco  Production,  Houston. 
U.S.  National  Museum  nos.  410130  (holotype,  cf  RV:  Text-fig.  1),  410131  (paratvpe,  9 LV:  PL 
14,  18,  fig.  1),  410132  (paratype,  cf  RV:  PI.  14,  18,  fig.  2),  410133  (paratype,  cf  LV:  PI.  14,  20.  fig. 
1),  410134  (paratype,  LV:  PI.  14,  20,  fig.  2).  All  from  the  type  locality  and  horizon  (locality 
83-EB-187,  188,  collected  by  E.  Brouwers,  1983). 

Short,  high,  rectangular  lateral  outline;  large  size;  weak  dimorphism.  Three  pairs  of  spines  in 
median  valve  area;  large,  strong  marginal  spines.  Wide  marginal  flange,  continuous  along  anterior 
and  venter.  Numerous  ventral  marginal  spines.  Spinose  anterodorsal  margin  with  weak  underlying 
flange.  Strong  posteroventral  spinose  prolongation.  Left  valve  hinge  has  anterior  socket  with 
ventral  rim;  elongate,  U-shaped  posterior  socket;  cylindrical  posteromedian  tooth;  weakly 
crenulate  median  bar. 


Explanation  of  Plate  14,  18 

Fig.  1,  $ LV,  ext.  lat.  (paratype,  410131,  1380/um  long);  fig.  2,  cf  RV,  ext.  lat.  (paratype,  410132.  1460/am  long). 
Scale  A (100/um;  xl25),  figs.  1,  2. 


Stereo-Atlas  of  Ostracod  Shells  14,  19 

Remarks: 


Pterygocythereis  vannieuwenhuisei  (3  of  4) 


Distribution: 


Pterygocythereis  ranges  from  the  Paleocene-Holocene,  occurring  commonly  throughout  the 
subtropical  and  temperate  N Atlantic  Ocean  and  rarely  in  the  subfrigid  Norwegian  Sea.  In  the 
northwestern  Atlantic  Ocean,  Pterygocythereis  occurs  in  the  southern  cold  temperate  zone,  but 
does  not  live  in  the  northern  cold  temperate  or  subfrigid  zones  of  the  western  N Atlantic. 
Pterygocythereis  vannieuwenhuisei  is  related  to  the  European  P.  mucronata-P.  jonesii  species 
complex  and  not  to  the  more  temperate  NW  Atlantic  P.  americana-P.  inexpectata  lineage. 
?Late  Miocene,  early-late  Pliocene  (to  2.48  Ma):  NE  Alaska,  three  localities  in  Colvillian-aged 
sediments  of  the  Gubik  Fm.  (Fish  Creek,  Kalikpik  R.,  Miluveach  Creek;  2.48  - 3.0  Ma,  late 
Pliocene;  Repenning  et  ah,  op.  cit.),  three  localities  in  the  upper  Nuwok  Member  of  the 
Sagavanirktok  Fm.  (Carter  Creek,  Barter  Is.,  Manning  Pt.;  ?late  Miocene,  lower  to  middle 
Pliocene). 


P.  vannieuwenhuia 


° 

icPm 

° 

a, 

~ d 

° 

Text-fig.  1.  Holotype  (cf  RV,  USNM  no.  410130), 
camera  lucida  drawing,  seen  in  transmitted  light. 


Text-fig.  2.  Plot  of  length  vs.  height  for  26  specimens 
from  the  type  locality. 


Explanation  of  Plate  14,  20 

Fig.  1,  cf  LV,  ext.  lat.  (paratype,  410133,  1280/um  long);  fig.  2,  LV,  int.  lat.  (paratype,  410134,  1300/um  long). 
Scale  A (100/am;  xl25),  figs.  1,  2. 


Stereo- Atlas  of  Ostracod  Shells  14,  18 


Pterygocythereis  vannieuwenhuisei  (2  of  4) 


Stereo-Atlas  of  Ostracod  Shells  14  (6)  21-24  (1987)  Muellerina  hazeli  (1  of  4) 

595.337.14  (119.1/119.9)  (261.4  : 162.082.24)  : 551.351/352 


ON  MUELLERINA  HAZELI  COLES  & CRONIN  sp.  nov. 

by  Graham  P.  Coles  & Thomas  M.  Cronin 
(University  College  of  Wales,  Aberystwyth  & U.S.  Geological  Survey,  Reston,  Virginia) 


Muellerina  hazeli  sp.  nov. 


Holotype: 


Type  locality: 
Derivation  of  name: 
Figured  specimens: 


British  Museum  (Nat.  Hist.)  no.  OS  12971,  9 LV. 

[Paratypes:  British  Museum  (Nat.  Hist.)  nos.  OS  12972-OS  12975.  Four  additional 
paratypes  have  been  deposited  in  the  U.S.  Museum  of  Natural  History:  USNM  nos. 

409239-409242). 

Off  the  Florida  Keys,  United  States  continental  slope;  approx,  lat.  24°  26'N,  long.  81°  38'W; 
Recent,  water  depth  107m. 

In  honour  of  Joseph  E.  Hazel,  in  recognition  of  his  studies  on  Muellerina  from  the  Atlantic  Coastal 
Plain  and  shelf. 

British  Museum  (Nat.  Hist.)  nos.  OS  12971  (holotype,  9 LV:  PI.  14,  22,  fig.  1;  PI.  14,  24,  fig.  1). 
OS  12972  (paratype,  9 RV:  PI.  14,  22,  fig.  2),  OS'l2973  (paratype,  cf  LV:  PI.  14.  22,  fig.  3).  OS 
12974  (paratype,  cf  RV:  PI.  14,  24,  fig.  2),  OS  12975  (paratype,  cf  car.:  PI.  14,  24,  fig.  3).  All  from 
the  type  locality  and  horizon. 


Explanation  of  Plate  14,  22 

Fig.  1,  9 LV,  ext.  lat.  (holotype,  OS  12971,  580/um  long);  fig.  2,  9 RV,  ext.  lat.  (paratype.  OS  12972.  570/am  long);  fig.  3,  Cf  LV.  ext. 

lat.  (paratype,  OS  12973,  550/u.m  long). 

Scale  A (100/am;  X130),  figs.  1-3. 


Stereo-Atlas  of  Ostracod  Shells  14,  23  Muellerina  hazeli  (3  of  4) 


Diagnosis: 


Remarks: 


Distribution: 


A species  of  Muellerina  characterised  by  small  size,  relatively  thick  shell,  simple  subovate  outline 
in  dorsal  view,  and  delicate  ornament  consisting  of  numerous  discrete  circular  to  ovate  fossae  with 
several  sharply  defined  narrow  muri  extending  both  above  and  below  the  muscle  scar  platform  and 
into  the  anterior  field  of  the  valve. 

M.  hazeli  most  closely  resembles  M.  ohmerti  Hazel,  1983,  but  is  distinctly  smaller,  being 
equivalent  in  size  to  the  A-l  instar  of  M.  ohmerti , and  has  a distinctive,  more  delicately  developed 
ornament.  M.  hazeli  rarely  occurs  sympatrically  with  M.  ohmerti  north  of  Cape  Hatteras  (above 
35°N),  but  is  more  abundant  in  deeper  water  on  the  upper  continental  slope,  whereas  M.  ohmerti  is 
a typical  shelf  species,  most  common  at  depths  between  25  and  175m  (Hazel  1970).  M.  hazeli  is 
both  the  smallest  and  the  most  southerly  distributed  extant  species  of  Muellerina.  It  is  believed  to 
have  evolved  from  its  parent  species,  M.  ohmerti , during  a high  sea  level  stand  in  the  late  Pliocene 
(Cronin  & Coles,  in  prep.),  and  has  since  undergone  little  morphological  change. 

Recent  of  the  Atlantic  continental  shelf  and  slope  from  the  Florida  Keys  (24°  25'N)  to  off  New 
York  at  the  head  of  Lydonia  Canyon  (40°  30'N).  M.  hazeli  lives  on  the  outer  shelf  and  upper  slope, 
most  commonly  between  75  and  250m,  having  a maximum  present-day  depth  range  of  35  to  382m. 
It  is  also  present  in  Pleistocene  sediments  in  cores  off  the  eastern  United  States  from  32°  04'N  to 
38°  22'N,  and  in  Pleistocene  outcrops  in  the  Norfolk  and  Wilmington  submarine  canyons. 


Explanation  of  Plate  14,  24 

Fig.  1,  9 LV,  int.  lat.  (holotype.  OS  12971.  580/xm  long);  fig.  2,  cf  RV,  int.  lat.  (paratype,  OS  12974,  530/u.m  long);  fig.  3,  cf  car., 
dorsal  (paratype,  OS  12975,  570/um  long). 

Scale  A (100/u.m;  X130),  figs.  1-3. 


Stereo-Atlas  of  Ostracod  Shells  14,  24 


Muellerina  hazeli  (4  of  4) 


Stereo-Atlas  of  Ostracod  Shells  14,  22 


Muellerina  hazeli  (2  of  4) 


Stereo-Atlas  of  Ostracod  Shells  14  (7)  25-28  (1987)  Healdianella  ? aremorica  (1  of  4) 

595.337.21  (113.51)  (44  : 161.002.47)  : 551.351  + 552.54 


ON  HEALDIANELLA  ? AREMORICA  CRASQUIN  sp.  nov. 

by  Sylvie  Crasquin 
(University  of  Lille,  France ) 


Healdianella  ? aremorica  sp.  nov. 

University  of  Lille;  France,  ostracode  Collection  (COUL)  no.  860,  cf  carapace. 

[Paratypes:  COUL  nos.  861,  862,  863,  865,  2155]. 

Port  Etroit  Quarry  (sample  no.  85  MA  1),  Laval  syncline,  Armorican  Massif.  France;  lat.  47°  50' 
54"  N,  long.  2°  39'  02"E.  Sable  Limestone,  uppermost  Tournaisian,  Carboniferous. 

From  the  latin  aremoricus , Armorica,  western  province  of  Gaul. 

University  of  Lille,  France,  ostracode  collection  (COUL)  nos.  860  (holotype,  cf  car.:  PI.  14,  26. 
fig.  1),  862  ($  car.:  PI.  14.  26,  fig.  2),  863  (9  car.:  PI.  14.  26,  fig.  3).  865  (9  car.:  PI.  14.  28,  fig.  1), 
861  (juv.  car.:  PI.  14,  28,  fig.  2),  864  (juv.  car.:  PI.  14,  28,  fig.  3),  2155  (cf  car.:  PI.  14,  28,  fig.  4). 
All  from  the  Sable  Limestone  of  type  locality;  uppermost  Tournaisian,  lower  Carboniferous. 


Holotype: 

Type  locality: 

Derivation  of  name: 
Figured  specimens: 


Explanation  of  Plate  14,  26 

Fig.  1,  Cf  car.,  rt.  lat.  (holotype,  COUL  860.  0.58  mm  long);  fig.  2,  9 car.,  rt.  lat.  (paratype.  COUL  862.  0.58  mm  long);  fig.  3,  9 car.. 

rt.  lat.  (paratype,  COUL  863,  0.60  mm  long). 

Scale  A (200  fim;  x 140),  fig.  1;  scale  B (200  yu.m:  x 85),  figs.  2,  3. 


Stereo-Atlas  of  Ostracod  Shells  14,  27  Healdianella  ? aremorica  (3  of  4) 


Diagnosis: 


Remarks: 


Distribution: 


Small,  smooth  species  (adults  0.52-0.63  mm  long)  doubtfully  assigned  to  Healdianella. 
Anterodorsal  border  straight;  anterior  border  with  a maximum  of  convexity  located  between  12 
and  lower  1/3  of  valve  height;  ventral  border  is  concave,  with  maximum  concavity  located  in  the 
anterior  1/3  of  valve  length;  posterior  border  broadly  rounded  with  maximum  convexity  located 
slightly  below  mid-height.  In  dorsal  view,  the  carapace  is  laterally  compressed  in  the  medial 
region.  Overlap  is  weak. 

Sexual  dimorphism:  heteromorphs  have  a more  obtuse  dorsal  angle  in  lateral  view,  and  in 
dorsal  view  are  wider  behind  a more  pronounced  median  stricture.  Tecnomorphs  have  a more 
acute  dorsal  angle  in  lateral  view  and  in  dorsal  view  are  virtually  of  equal  width  throughout,  the 
median  stricture  being  poorly  developed. 

This  species  looks  like  Healdianella  linevensis  Tschigova,  1958  from  the  upper  Tournaisian  of  the 
Saratov-Leningrad  area  ( Trudy  V.N.I.G.R.I. , 14).  H.  linevensis  differs  in  having  a smaller 
length/height  ratio,  a more  convex  anterodorsal  border  and  an  anterior  border  which  is  not 
laterally  compressed. 

H.  ? aremorica  is  assigned  to  Headianella  with  doubt  because  in  dorsal  view  its  carapace  is 
laterally  compressed  in  the  medial  region,  a characteristic  not  observed  in  other  species  of  that 
genus. 

Laval  syncline,  Armorican  Massif,  France:  uppermost  Tournaisian-lower  Visean.  lower  Carbo- 
niferous. 


Explanation  of  Plage  14,  28 

Fig.  1,  9 car.,  dors,  (paratype.  COUL  865,  0.58  mm):  fig.  2.  juv.  car..  It.  lat.  (paratype,  COUL  861. 0.47  mm  long);  fig.  3,  juv.  car.,  rt. 

lat.  (paratype,  COUL  864,  0.40  mm  long);  fig.  4,  cf  car.,  dors,  (paratype,  COUL  2155.  0.55  mm  long). 

Scale  A (200  fim;  x 125),  figs.  1,  3,  4;  scale  B (200  yum:  x 100),  fig.  2. 


Healdianella  ? aremorica  (2  of  4) 


Stereo-Atlas  of  Ostracod  Shells  14,  26 


Stereo-Atlas  of  Ostracod  Shells  14,  28 


Healdianella  ? aremorica  (4  of  4) 


Stereo-Atlas  of  Ostracod  Shells  14  (8)  29-32  (1987) 
595.337.14  (116.331)  (65  : 161.004.35)  : 551.35 


Maghrebeis  tuberculata  ( 1 of  4) 


Derivation  of  name: 
Diagnosis: 


ON  MAGHREBEIS  TUBERCUEATA  MAJORAN  gen.  et  sp.  nov. 

by  S.  Majoran 

(Department  of  Historical  Geology  and  Palaeontology,  University  of  Uppsala,  Sweden) 

Genus  MAGHREBEIS  gen.  nov. 

Type-species:  Maghrebeis  tuberculata  sp.  nov. 

From  the  North  African  province  of  Maghreb  (including  Morocco,  Algeria  and  Tunisia). 
Carapace  small,  subtriangular,  inequivalved.  Left  valve  larger,  overhanging  posterior,  ventral  and 
anterior  margins  of  right  valve.  Ventral  margin  convex,  converging  posteriorly  with  straight  dorsal 
margin.  Thick,  swollen  ridge  runs  along  evenly  rounded  anterior  margin,  denticulated  prominently 
only  on  right  valve,  seldom  and  only  feebly  on  left  valve.  Caudal  process  triangular,  pointed  at 
mid-height  and  armed  with  a swollen  ridge.  Ornament  polymorphic.  Ventromedian  and 
dorsomedian  areas  bear  pronounced  lobate  tubercles.  Lateral  surface  variously  pitted,  ventral 
surface  with  4-5  fine  longitudinal  ribs.  Hinge  ear  of  left  valve  is  large,  forms  a thick,  hook-like 
protuberance  that  overlaps  right  valve.  Circular  eye  tubercle  and  ovate  adductor  muscle  tubercle 
prominent.  Hinge  amphidont/heterodont;  right  valve  has  large  posterior  tooth  and  strong  anterior 
tooth  with  a large,  spherical  distal  part  fused  to  a smaller  proximal  part. 

Similar  outline  to  Veenia  Butler  & Jones,  1957  and  Veeniacythereis  Griindel.  1973.  which  differ  by 
being  larger,  having  3 longitudinal  ridges  and  lacking  the  curved,  left  hinge  ear  of  Maghrebeis.  The 
left  hinges  of  all  three  are  similar,  but  the  right  hinge  of  Maghrebeis  differs  in  having  a modified 
anterior  tooth.  Veenia  also  differs  by  its  usually  more  pointed  caudal  process,  and  Veeniacythereis 
by  its  feeble  or  absent  subcentral  tubercle. 

Cythereis?  sp.  of  Rosenfeld  & Raab  (Bull.  geol.  Surv.  Israel,  62.  pi.  2.  figs.  45-46.  1974; 
upper  Cenomanian,  Israel)  probably  belongs  to  Maghrebeis  since  it  differs  only  by  its  smooth 


Remarks: 


Explanation  of  Plate  14,  30 

Fig.  1,  9?car.,  It.  lat.  (holotype,  PMAL1,  500/u.m  long);  fig.  2,  9?  car.,  dors..  (PMAL2,  530/xm  long);  fig.  3.  9?  RV,  int.  lat.  (PMAL3. 
500/j.m  long);  fig.  4,  9 ? LV,  int.  lat.,  (PMAL4,  510/xm  long).  Scale  A (lOO^m;  xl30),  figs.  1-4. 


Stereo-Atlas  of  Ostracod 

Remarks:  (cont.) 


Holotype: 
Type  locality: 
Derivation  of  name: 
Figured  specimens: 


Diagnosis: 


Distribution: 


Shells  14,  31  Maghrebeis  tuberculata  (3  of  4) 

surface  and  possibly  having  one  less  dorsal  tubercle.  Also  possibly  congeneric  is  Cythereis 
lindiensis  Bate,  1969  as  reported  by  Grosdidier  ( Revue  Inst.  fr.  Petrole.,  28.  pi.  13.  fig.  104.  1973), 
which  appears  to  be  slightly  larger  and  has  more  irregular  dorsomedian  and  ventromedian 
tuberculation,  a less  pronounced  subcentral  tubercle  and  a smooth  surface.  Further  differences  are 
revealed  by  the  original  description  and  re-illustrated  type  material  of  C.  lindiensis  (Bate  & 
Mellish,  Stereo-Atlas  Ostracod  Shells,  13,  59-62.  1986).  Another  externally  similar,  considerably 
larger  species  is  Grosdidier's  Cythereis  gr.  malzi  Bischoff.  1963  (Revue  Inst.  fr.  Petrole,  28,  pi.  14. 
fig.  105,  1973). 

Maghrebeis  tuberculata  sp.  nov. 

Palaeontological  Museum,  University  of  Uppsala,  Sweden,  no.  PMAL1,  9?  carapace. 
Approx.  14km  SW  of  Tocqueville,  Algeria  (approx,  lat.  35°  52'N,  long.  4°  55'E);  Cenomanian. 
Latin,  from  the  prominent  dorsomedian  and  ventromedian  tubercles. 

Palaeontological  Museum,  University  of  Uppsala.  Sweden,  nos.  PMAL1  (holotype.  9?  car.:  PI. 
14,  30,  fig.  1),  PMAL2  (9?  car.:  PI.  14,  30,  fig.  2).  PMAL3  (9?  RV:  PI.  14.  30.  fig.  3).  PMAL4  (9? 
LV:  PI.  14,  30,  fig.  4),  PMAL5  (9?  car.:  PI.  14,  32,  fig.  2).  PMAL6  (9?  car.:  PI.  14,  32,  fig.  1), 
PMAL7  (cf?  car.:  PI.  14,  32,  figs.  3,  4).  All  from  the  type  locality  and  horizon. 

Maghrebeis  with  fine  network  of  small  pits,  and  3 smooth,  lobe-like  tubercles  respectively  on 
dorsomedian  and  ventromedian  regions.  Two  additional,  smaller  tubercles  vertically  arranged  on 
posteromedian  area.  Swollen  anterior  and  posterior  ridges,  pronounced  eye  tubercle,  and  ovate, 
adductor  muscle  tubercle  are  all  smooth  as  are  also  some  narrow,  longitudinal  fields  on  ventral 
surface.  Ornament  polymorphic  with  respect  to  size  and  configuration  of  dorsomedian  and 
ventromedian  tubercles,  strength  of  anterior  and  posterior  ridges,  and  presence  of  denticles  along 
ventral  section  of  caudal  process.  Shape  differences  might  reflect  sexual  dimorphism:  one  type 
being  dorsoventrally  and  laterally  more  compressed  (=  cf?)- 
Uppermost  Albian  (or  lower  Cenomanian)  to  middle  Cenomanian  of  N Africa. 


Explanation  of  Plate  14,  32 

Fig.  1,  9?  car.,  rt.  lat.  (PMAL  6,  500/um  long);  fig.  2,  9?  car.,  vent.,  showing  pitted  surface  with  smooth,  narrow,  longitudinal  fields 
(PMAL5,  500/u.m  long);  figs.  3-4,  cf?  car.  (compressed  morph),  (PMAL7,  500/xm  long):  fig.  3,  car.,  rt.  lat.;  fig.  4.  detail  of 
dorsomedian  tuberculation.  Scale  A (100pim;  x!30),  figs.  1-3;  scale  B (lOOpun;  x280),  fig.  4. 


Stereo-Atlas  of  Ostracod  Shells  14,  32 


Maghrebeis  tuberculata  (4  of  4) 


Stereo-Atlas  of  Ostracod  Shells  14  (9)  33-36  (1987)  Howeina  camptocytheroidea  ( 1 of  4) 

595.337.14  (118.22  + 119.9)  (520  : 161.140.41  + 520  : 161.140.42)  551.351 

ON  HOWEINA  CAMPTOCYTHEROIDEA  HANAI 

by  Noriyuki  Ikeya  & Ellen  Compton-Gooding 
(Shizuoka  University,  Shizuoka,  Japan  & U.S.  Geological  Survey,  Reston,  V A) 

Genus  HOWEINA  Hanai,  1957 

Type-species  (by  original  designation):  Howeina  camptocytheroidea  Hanai,  1957 
Diagnosis:  Ovate  Cytheruridae,  right  valve  overlapping  on  dorsal  margin,  left  valve  overlapping  on  ventral 

margin.  Greatest  height  anterior,  ventral  margin  nearly  straight  with  a slight  alate  projection,  eye 
tubercle  indistinct.  Inner  margin  has  modified  S-shape  along  posterior  margin. 

Remarks:  Howeina  resembles  Semicytherura  Wagner,  1957  (see  Whittaker,  Stereo-Atlas  Ostracod  Shells,  2, 

69-92,  1974);  some  might  consider  them  synonymous  since  both  have  S-shaped  posterior  inner 
margins,  but  the  validity  of  this  criterion  for  recognising  Semicytherura  is  questionable.  In  any 
case,  right  valves  of  Howeina  have  a large  elongate  anterior  tooth,  a knob-like  posterior  tooth  and 
a smooth  median  element;  in  Semicytherura  anterior  and  posterior  teeth  of  the  right  valve  are 
crenulate  or  have  2-3  knob-like  projections,  and  the  median  element  is  smooth  in  the  center  with 
sockets  at  its  ends. 

Howeina  camptocytheroidea  Hanai.  1957 

1957  Howeina  camptocytheroidea  sp.  nov.  T.  Hanai,  J.  Fac.  Sci.  Tokyo  Univ.,  sec.  2,  11,  22-23,  pi.  3,  figs.  4a-c,  text-figs.  5a,  b. 

1961  Howeina  camptocytheroidea  Hanai;  T.  Hanai,  ibid.,  13,  358,  text-fig.  2,  figs.  5a,  b. 

1971  Howeina  camptocytheroidea  Hanai;  K.  Ishizaki,  Tohoku  Univ.  Sci.  Rept.,  2nd  ser.,  (Geol.),  43,  79-80,  pi.  2,  fig.  21. 

1977  Howeina  camptocytheroidea  Hanai;  T.  Hanai  et  al.,  Bull.  Univ.  Mus.  Tokyo,  12,  56.  pi.  3,  figs.  1-7. 


Explanation  of  Plate  14,  34 

Fig.  1,  cf  LV,  ext.  lat.  (IGSU-0-122,  618  pm  long);  fig.  2,  cf  car.,  ext.  dors.  (IGSU-0-126.  653  yum  long);  fig.  3,  cf  RV,  ext.  lat. 
(IGSlJ-0-123,  613  pm  long);  fig.  4,  9 car.,  ext.  vent.  (IGSU-0-121.  605  yum  long);  fig.  5,  9 RV,  ext.  lat.  (IGSU-0-124,  625  pm 
long).  Scale  A (100  yum;  x 100),  figs.  1-5. 


Type  locality: 
Figured  specimens: 

Diagnosis: 

Remarks: 


Stereo-Atlas  of  Ostracod  Shells  14,  35  Howeina  camptocytheroidea  (3  of  4) 

Holotype:  University  Museum,  University  of  Tokyo,  Tokyo,  Japan,  no.  UMUT-CA-2612.  9 right  valve. 

[Paratypes:  nos.  UMUT-CA-2613-2615] 

Upper  Pliocene  Setana  Formation  at  Kaigarazawa,  about  500m  W of  Nishinosawa,  Kuromatsu- 
nai,  Suttsu-gun,  Hokkaido  (lat.  42°  39'  37"N,  long.  140°  17'  37"E). 

Institute  of  Geosciences,  Shizuoka  University  (IGSU)  nos.  0-121  (9  car.:  PI.  14,  34,  fig.  4),  0-122 
(Cf  LV:  PI.  14,  34,  fig.  1),  0-123  (cf  RV:  PI.  14,  34,  fig.  3;  PI.  14,  36,  fig.  7),  0-124  (9  RV:  PI.  14, 
34,  fig.  5;  PI.  14,  36,  figs.  4-6),  0-125  (9  LV:  PI.  14,  36,  figs.  1-3),  0-126  (cf  car.:  PI.  14,  34,  fig.  2). 
0-121  is  a Recent  specimen  from  Mutsu  Bay,  northern  Honshu  (lat.  41°  20'N,  long.  140°  55'E). 
0-122-126  are  from  the  type  locality;  0-122,123  are  disarticulated  valves  of  the  same  individual. 
The  valve  surface  has  a pattern  of  pits  that  run  parallel  along  the  posterior  and  dorsal  margins  and 
somewhat  longitudinally  in  the  center  of  the  valve.  The  anterior  and  posterior  areas  have  a pattern 
of  irregular  polygons  delineated  by  fine  ridges.  The  flat  ventral  margin  has  a series  of  ridges  that 
run  parallel  to  it.  The  posteroventral  area  is  slightly  depressed  behind  the  alate  projection. 
H.  higashimeyaensis  Ishizaki,  1971,  H.  leptocytheroidea  (Hanai,  1957),  and  H.  neoleptocytheroidea 
(Ishizaki,  1966)  each  possess  a distinctive  pattern  of  prominent  ridges  and  varying  degrees  of 
reticulation.  They  also  have  caudal  processes  that  are  more  obvious  than  that  of  H. 
camptocytheroidea.  Specimens  illustrated  by  McDougall,  Brouwers  & Smith  (Bull,  U.S.  Geol. 
Surv.,  1598,  56,  pi.  10,  figs.  1,2,  1986)  from  Prudhoe  Bay,  Alaska,  as  Cytherura  sp.  B and 
Cytherura  sp.  C.,  appear  to  be  very  similar  to  H.  camptocytheroidea. 

A cold  water  species,  H.  camptocytheroidea  is  currently  living  in  Suttsu  and  Uchiura  Bays, 
southern  Hokkaido;  Aomori  and  Mutsu  Bays,  Aomori  Prefecture;  and  Otsuchi  Bay,  Iwate 
Prefecture.  Late  Pleistocene  occurrences:  the  Nopporo  Fm.  Hokkaido;  Shibikawa  and  Anden 
formations,  Akita  Prefecture;  Hashidate  Fm.  Ishikawa  Prefecture;  and  Jizodo,  Yabu  and 
Kiyokawa  formations  in  Chiba  Prefecture.  In  the  late  Pliocene,  it  occurs  at  the  type  locality;  the 
Tomikawa  Fm.  Hokkaido;  the  Hamada  Fm.  Aomori  Prefecture;  and  the  Junicho  Fm.  Toyama 

Prefecture. 

Explanation  of  Plate  14,  36 

Fig.  1-3,  9 LV  (IGSU-0-125,  650  yu.rn  long):  fig.  1,  int.  lat.;  fig.  2,  post,  hinge;  fig.  3,  ant.  hinge;  figs.  4-6,  9 RV  (IGSU-0-124):  fig.  4, 
inf.  lat.,  fig.  5,  ant.  hinge;  fig.  6,  post,  hinge;  fig.  7,  cf  RV,  int.  muse,  sc.,  dorsal  is  to  right  (IGSU-0-123). 

Scale  A (100  yum;  X 100),  figs.  1,  4;  scale  B (100  yum;  x 160),  figs.  2,  3,  5,  6;  scale  C (10  yum;  x 540),  fig.  7. 


Distribution: 


Stereo-Atlas  of  Ostracod  Shells  14,  36 


Howeina  camptocytheroidea  (4  of  4) 


Stereo- Atlas  of  Ostracod  Shells  14,  34 


Howeina  camptocytheroidea  (2  of  4) 


Stereo-Atlas  of  Ostracod  Shells  14  (10)  37-40  (1987) 
593.337.14  (116.333.3)  (492:161.005.50)  : 551.35 


Spinoleberis  eximia  ( 1 of  4) 


ON  SPINOLEBERIS  EXIMIA  (BOSQUET) 

by  J.  F.  Babinot  & J.  P.  Colin 

(Universite  de  Provence,  Marseille  and  Esso  Production  Research- European  Lab.,  Begles,  France) 

Genus  SPINOLEBERIS  Deroo,  1966 
Type-species:  Cythere  eximia  Bosquet,  1854  (by  original  designation). 

Diagnosis:  Small-sized  trachyleberidid  (less  than  650/am)  characterized  by  a well-marked  hemispherical, 

sub-central  tubercle;  ventral  ridge  reduced  to  a strong  posterior  spinose  tubercle  and  a median 
lamellar  spine;  strong  spinose  tubercle  present  at  the  postero- dorsal  angle  and  a vertical  spine  on 
the  middle  part  of  the  dorsal  margin.  A ridge  connects  the  eye-tubercle  and  the  sub-central 
tubercle;  a weak  longitudinal  median  ridge  may  be  present;  anterior  margin  bordered  by  two  rows 
of  strong  spines.  Surface  of  the  valves  smooth  to  very  finely  reticulate  mostly  on  the  anterior  half. 
Sexual  dimorphism  distinct,  males  being  longer  than  females.  Amphidont  hinge.  Anterior 
marginal  zone  of  medium  width  with  about  20  straight  pore  canals.  Muscle  scars:  three  small  scars 
disposed  in  a V-shape  or  a V-shaped  scar  with  an  additional  round  scar  above  the  posterior 
branch;  four  adductor  scars,  the  upper  one  being  divided  into  two,  the  one  below  into  three. 

Remarks:  The  genus  Spinoleberis  is  relatively  common  in  the  late  Cretaceous  of  Western  and  Central 

Europe.  Typical  species  are  restricted  to  the  Campanian-Maastrichtian.  Cenomanian  and 
Turonian  species  such  as  S.  petrocorica  (Damotte,  Rev.  Micropal , 14,  1,  1973),  S.  krejcii  Pokorny 
( Acta  Univ.  Carolinae  Geoi,  4,  1968)  and  S.  ectypus  Babinot  ( Geobios , 6,  1,  1973)  have  a rather 
different  morphology;  they  are  deeply  reticulate  and  do  not  display  the  characteristic  spinose 
tubercles.  Species  attributed  to  the  genus  Spinoleberis  by  Donze  (1970),  have  been  recently  placed 
in  the  newly  errected  genus  Navarracy there  Colin  & Rodriguez-Lazaro  ( Stereo-Atlas  Ostracod 
Shells,  13,  63-66,  1986). 


Fig.  1,  $ car.,  ext.  rt.  lat.  (20648-49,  560 /xm  long) 
560 p.m  long).  Scale  A (250 pm:  xllO),  figs. 


Explanation  of  Plate  14,  38 

fig.  2,  cf  LV,  ext.  lat.  (20646-47,  550/u.m  long);  fig.  3,  cf  RV,  ext.  lat.  (20642-43. 
1-3. 


1854 

1936 

1958 

1966 

1966 

1983 


Type  locality: 
Figured  specimens: 


Stereo-Atlas  of  Ostracod  Shells  14,  39  Spinoleberis  eximia  (3  of  4) 

Spinoleberis  eximia  (Bosquet,  1854) 

Cythere  eximia  n.  sp.  J.  Bosquet,  Verhandel.  geol.  beschr.  kaart  Nederland , 2,  106,  pi.  7.  figs.  6a-d. 

Cythereis  eximia  (Bosquet);  J.  E.  van  Veen,  Nat.  hist.  Maandbl.,  25,  11-12,  26,  pi.  7,  figs.  1-6. 

Cythereis  eximia  (Bosquet);  H.  Howe  & L.  Laurencich,  Introduction  to  the  study  of  Cretaceous  Ostracoda , 196-197. 
Spinoleberis  eximia  (Bosquet);  G.  Deroo,  Meded.  geol.  Sticht.,  C,  2,  2,  165-166,  pi.  6,  figs.  72-74,  pi.  26,  figs.  822-824. 
Cythereis  eximia  (Bosquet);  E.  Herrig,  Paldont.  Abh.,  A,  2,  801-802.  pi.  18,  figs.  1-10,  pi.  19,  fig.  1. 

Spinoleberis  eximia  (Bosquet);  B.  Clarke,  Mitt.  Geol. -Paldont.  Inst.  Univ.  Hamburg,  54,  110-111,  pi.  7,  figs.  11-12. 
Holotype:  Material  deposited  in  the  collections  of  the  Institut  Royal  des  Sciences  Naturelles  de  Belgique, 

Brussels  under  the  reference  “Cretace  Ostracodes  87  Arthr.  Sec.  I,  Cret.”,  slide  no.  44. 
Late  Maastrichtian  of  St.  Pietersburg,  near  Maastricht,  southern  Limburg,  the  Netherlands. 
These  are  deposited  in  the  collections  of  Esso  Production  Research  - European  Laboratories  at 
Begles,  France  and  the  numbers  all  carry  the  prefix  EPR-E.  EPR-E  20648-49  (2  car. : PI.  14.  38. 
fig.  1),  20646-47  (Cf  LV:  PI.  14,  38,  fig.  2),  20642-4 3 (cf  RV:  PI.  14,  38,  fig.  3).  20650-51  (2  LV: 
PL  14,  40,  fig.  1),  20654-55  (cf  car.:  PI.  14,  40,  fig.  2),  20816-17  (2  RV:  PI.  14,  40,  fig.  3).  All 
figured  specimens  are  from  Puits  Maurits  (250.5m),  Maastricht,  southern  Limburg,  The 
Netherlands;  late  Maastrichtian. 

As  for  the  genus.  The  surface  of  the  muri  of  the  reticulation  is  very  finely  pitted.  A little  knob 
occurs  in  the  middle  of  each  mesh. 

Deroo  (1966),  illustrated  several  species  of  the  genus  Spinoleberis  in  the  type  Maastrichtian.  Most 
of  the  species  are  very  similar  to  S.  eximia  and  therefore  extremely  difficult  to  differentiate. 
Whether  they  are  different  species  or  merely  ecotypes  is  highly  questionable.  These  are 
S.  eximioides  (van  Veen)  and  S. pseudoeximia  Deroo.  Cythereis  symmetrica  van  Veen,  1936  (Nat. 
Hist.  Maandbl.,  25,  1 1—12)  is  considered  by  Deroo  (1966)  and  Clarke  (1983)  to  be  a juvenile  of 
S.  eximia,  by  Howe  & Laurencich  (1958).  (1965)  to  belong  in  S.  tuberosa  (Jones  & Hinde)  and  by 
Szczechura  (1965)  to  belong  in  S.  spinifera  (van  Veen). 

Late  Maastrichtian  of  the  Netherlands  and  Belgium.  Early  to  late  Maastrichtian  of  Germany. 


Diagnosis: 


Remarks: 


Distribution: 

Explanation  of  Plate  14,  40 

Fig.  1,  2 LV,  int.  lat.  (20650-51,  575/xm  long);  fig.  2,  cf  car.,  ext.  dors.  (20654-55,  555p.m  long);  fig.  3,  2 RV,  int.  lat.  (20816-17, 
545/u.m  long).  Scale  A (250/u.m;  XllO),  figs.  1-3. 


Spinoleberis  eximia  (2  of  4) 


Stereo-Atlas  of  Ostracod  Shells  14,  40 


Stereo-Atlas  of  Ostracod  Shells  14,  38 


Spinoleberis  eximia  (4  of  4) 


Stereo-Atlas  of  Ostracod  Shells  14(11)  41-44  (1987)  Kovalevskiella  caudata  (1  of  4) 

(118.21)  (44  : 162.001.44)  : 551.312.4  4-  552.54 

ON  KOVALEVSKIELLA  CAUDATA  (LUTZ) 

by  P.  Carbonel,  J.-P.  Colin  & L.  Londeix 
( University  of  Bordeaux,  Talence  & Esso  Production  Research,  Begles,  France) 

Kovalevskiella  caudata  (Lutz,  1965) 

1965  Gomphocythere  caudata  sp.  nov.  A.  K.  Lutz,  Geol.  Jahrb.,  82,  311,  text-fig.  27,  pi.  13,  figs.  1,  2. 

1969  Cordocythere  caudata  (Lutz);  G.  Carbonnel  & S.  Ritzkowski,  Arch.  Sci.  (Geneve),  22(1),  60. 

1980  Kovalevskiella  caudata  (Lutz);  J.-P.  Colin  & D.  Danielopol,  Paleobiol,  continent.,  11(1),  32,  37,  fig.  17. 

1985  Kovalevskiella  caudata  (Lutz);  P.  Carbonel,  Bull.  Centres.  Rech.  Explor.-Prod.  Elf- Aquitaine,  Mem.  9,  pi.  90,  figs.  7-10. 

1986  Kovalevskiella  caudata  (Lutz);  P.  Carbonel,  J.-P.  Colin,  D.  L.  Danielopol  & L.  Londeix,  Geobios,  19(6),  pi.  1,  figs.  4-7. 


Holotype: 
Type  locality: 

Figured  specimens: 


Diagnosis: 


Bundesanstalt  fur  Bodenforschung,  Hanover,  no.  5421,  LV.  [Paratype:  no.  5420,  LV] 

Road  cut  between  Undorf  and  Nittendorf  near  Regensburg.  Bavaria,  Federal  Republic  of 
Germany;  Tortonian,  Late  Miocene;  freshwater  molasse. 

Dept.  Geol.  & Oceanography,  Univ.  Bordeaux  I,  CO  nos.  5103  (LV;  PL  14,  42.  figs.  1-3;  PI.  14. 
44,  fig.  1),  5104  (RV:  PI.  14,  42,  figs.  4-6),  5105  (car.:  PI.  14,  44,  figs.  4,  5),  5106  (LV  juv.:  PI.  14. 
44,  fig.  2),  5107  (RV  juv.:  PI.  14,  44,  fig.  3),  5108  (LV  juv.:  PI.  14,  44.  fig.  6).  Aquitanian, 
Miocene,  of  Le  Moras,  near  Labrede,  Gironde,  France;  lat.  44°  41 'N,  long.  0°  34'W.  Original, 
German  material  could  not  be  photographed. 

Carapace  subrectangular,  rounded  anterior  and  posterior  extremities;  ornament  typical  of  genus: 
regularly  disposed  pustules.  Well  developed  sulcus;  large  brood  pouch.  RV  larger  than  LV;  both 
cardinal  hinge  elements  on  LV  trilobate.  No  sexual  dimorphism.  Tw'o  strong  denticles  on  the 
posteroventral  part  of  LV. 


Explanation  of  Plate  14,  42 

Figs.  1-3,  LV  (CO  5103,  430/xm  long);  fig.  1,  ext.  lat.;  fig.  2,  int.  lat.  hinge;  fig.  3,  int.  lat.  Figs.  4-6.  RV  (CO  5104,  433/am  long);  fig.  4, 
int.  lat.;  fig.  5,  ext.  lat.;  fig.  6,  int.  lat.  hinge.  Scale  A (200/luti;  xl35),  figs.  1,  3-5;  scale  B (200/i.m;  x205),  figs.  2,  6. 


Stereo-Atlas  of  Ostracod  Shells  14,  43  Kovalevskiella  caudata  (3  of  4) 

Remarks:  Like  other  Kovalevskiella,  K.  caudata  is  parthenogenetic.  It  differs  by  the  presence  of  2 strong  denticles  on 

the  posteroventral  part  of  the  left  valve.  Denticles  are  also  present  in  larval  stages,  but  only  in  the  right  valve. 
In  the  French  locality  studied,  this  species  lived  in  a lagoonal  to  lacustrine  environment  (in  oligo-to 
mesohaline  waters)  on  very  fine  grained,  marl  bottom  sediment.  K.  caudata  is  associated  with  Neocyprideis 
aquitanica  Moyes  or  with  Candonopsis  and  Limnocy there , and  always  with  poorly  diversified  faunas.  When 
the  waters  become  fresh  and  more  stable,  Kovalevskiella  disappears.  Lutz  (1965)  described  K.  caudata  from 
coaly  marls  in  a freshwater  molasse  deposit.  Its  epibenthic  life-style  is  very  different  to  the  hypogean  or 
interstitial  habitats  of  Recent  Kovalevskiella  (Colin  & Danielopol  1980;  Carbonel  et  al.,  1986). 

Distribution:  Miocene  (Tortonian)  near  Regensburg,  Germany  (Lutz  1965);  Miocene  (Aquitanian)  near  Bordeaux,  France 

(Carbonel  1985;  Carbonel  et  al.  1986). 


Text-fig.  1.  Size  dispersion  of  116  left  and 
right  valves  of  K.  caudata  from  Le  Moras, 
near  Labrede,  Gironde,  SW  France. 


Explanation  of  Plate  14,  44 

Fig.  1,  LV  ext.  dors.  (CO  5103,  430p,m  long);  fig.  2,  LV  juv.-l,  ext.  lat.  (CO  5106,  340/u.m  long);  fig.  3,  RV  juv. -2,  ext.  lat.  (CO  5107 
285/xm  long).  Figs.  4,  5,  car.  (CO  5105,  420/u.m  long):  fig.  4,  ext.  dors.;  fig.  5,  ext.  vent.  Fig.  6,  LV  juv. -3,  ext.  lat.  (CO  5108,  215pim 
long).  Scale  A (200/xm;  xl35),  figs.  1-6. 


250 


Adults 

’ ..-U* 

I •> 

¥ • 

A:' 


200  ' 


150  - 


LV 

RV 


300 


350 

Length  (um) 


450 


Stereo-Atlas  of  Ostracod  Shells  14  (12)  45-48  (1987)  Calocaria  maurae  (1  of  4) 

595.339.1  (113.333)  (64  : 162.008.31)  : 551.35  + 552.52 


ON  CALOCARIA  MAURAE  VANNIER  gen.  et  sp.  nov 


by  Jean  Vannier 
(University  of  Rennes,  France) 

Derivation  of  name: 

Genus  CALOCARIA  gen.  nov. 

Type-species:  Calocaria  maurae  sp.  nov. 

From  the  Greek  karia , a walnut  and  kalos,  beautiful;  alluding  to  the  shell  shape  and  lateral 
ornament.  Gender  feminine. 

Diagnosis: 

Myodocopid  ostracode,  oval  in  outline.  Length  3.5mm;  adults  have  a length:height  ratio  of 
approximately  1.1.  Prominent  anterior  rostrum  and  rostral  incisure.  Composite  external 
ornament:  pattern  of  coarse  ridges  running  obliquely  to  the  ventral  and  dorsal  margins,  converging 
towards  the  middle  of  the  valve  and  connected  ventrally  to  a continuous  marginal  ridge; 
posteriorly  to  mid-length,  ornament  consists  of  a linear  alignment  of  more  and  less  coalescent 
tubercles  laterally  merging  with  corrugations.  Small  arcuate  muscle  scar  impression. 

Remarks: 

This  new  genus  shares  many  similarities  (rostrum,  simple  muscle  scar  impression,  oval  outline) 
with  other  Silurian  ‘cypridinids'  and  is  tentatively  included  within  this  group.  Nevertheless,  the 
composite  ornament  of  Calocaria  is  comparable  to  that  of  Silurian  ‘bolbozoids’  (see  Siveter, 
Vannier  & Palmer,  Palaeontology , text-fig.  4,  in  press , 1987)  but  neither  the  distinctive 
anterodorsal  bulb  nor  sulcus  typical  of  that  group  occur  in  Calocaria.  By  its  well  developed 
ornament  Calocaria  is  distinguished  from  any  other  Silurian  ‘cypridinids',  which  are  mainly 
smooth  (see  Siveter,  Vannier  & Palmer,  Palaeontology , pis.  2,  3,  5,  in  press , 1987).  As  with 
numerous  myodocopids  from  the  Silurian  of  Europe,  most  specimens  of  Calocaria  maurae  show 
‘plastic'  deformation  of  the  valves,  suggesting  a rather  thin,  flimsy  shell. 

Explanation  of  Plate  14,  46 

Figs.  1-3,  RV  (holotype,  IGR  33100,  3055/u.m  long):  fig.  1,  ext.  lat. ; fig.  2,  ext.  vent,  obi.;  fig.  3,  ornament  of  lateral  surface. 
Scale  A (750/iun;  xl8),  figs.  1,  2;  scale  B ( 100/am;  x75),  fig.  3. 

Stereo-Atlas  of  Ostracod  Shells  14,  47  Calocaria  maurae  (3  of  4) 

Calocaria  maurae  sp.  nov. 


Holotype: 

Institut  de  Geologie,  University  of  Rennes  (IGR),  France,  coll.  no.  33100;  RV. 
(Paratypes:  IGR  coll.  nos.  33101,  LV;  33103,  RV;  33104,  LV;  33106.  LV], 

Type-locality: 

Siltstones  and  mudstones  in  the  Talmakent  section  near  Talmakent  (sample  TA  84452  of  J.  J. 
Cornee  collections,  University  of  Aix-Marseille,  France),  Haut-Atlas,  Morocco;  lat.  31°  52’N, 
long.  7°  45'W.  Upper  part  of  the  Silurian;  as  determined  by  J.  J.  Cornee  (work  in  progress). 

Derivation  of  name: 
Figured  specimens: 

From  maura , Moorish,  alluding  to  the  region  where  this  species  occurs. 

Inst,  de  Geologie,  Univ.  Rennes  (IGR),  coll.  nos.  33100  (holotype,  RV:  PI.  14,  46,  figs.  1-3;  PI.  14, 
48,  figs.  1,  2)  and  33101  (paratype,  LV:  PI.  14,  48,  figs.  3-6).  From  type  locality;  latex  casts. 

Diagnosis: 

Remarks: 

As  for  the  genus.  Monotypic. 

C.  maurae  is  the  first  Silurian  myodocopid  to  be  described  from  Africa.  In  the  type  locality,  it  is 
associated  with  numerous  other  myodocopid  ostracodes,  both  ‘bolbozoids"  and  ‘cypridinids-.  In 
this  respect,  this  fauna  is  comparable  to  that  recently  documented  from  organic-rich.  Silurian 
sediments  of  Britain  and  France  (Siveter,  et  al .,  op.  cit . , in  press).  As  a prelude  to  their  further 
systematic  studies  of  Silurian  myodocopids  the  latter  authors  have  noted  the  occurrence  of  similar 
myodocopid  faunas  in  the  same  type  of  deposits  (black  to  terrigenous  mudstones)  from 
northwestern  Europe  (e.g.  Ludlow  Series  in  Wales  and  the  Armorican  Massif,  France),  eastern 
Europe  (Ludlow  Series  of  Bohemia,  Czechoslovakia)  and  now  North  Africa  (herein).  An  outer 
shelf  to  shelf  margin  or  even  shelf  slope  environment  is  inferred,  from  faunal  and  sedimentological 
evidence,  for  the  myodocopid  occurrences  in  Europe  (see  Siveter.  et  al.,  op.  cit.,  in  press)  and  is 

Distribution: 

Acknowledgements: 

also  likely  in  the  case  of  the  Moroccan  material. 

At  present,  known  only  from  the  type  locality. 

To  J.  J.  Cornee  (University  of  Aix-Marseille)  for  allowing  me  to  study  his  material  and  to  the 
Humboldt  Foundation  (Bonn)  for  my  Research  Fellowship  at  Hamburg  University. 

Explanation  of  Plate  14,  48 

Figs.  1.  2.  RV  (holotype,  IGR  33100,  3055/j.m  long):  fig.  1,  ext.  ant.  obi.;  fig.  2,  ext.  post.  obi.  Figs.  3-6,  LV  (IGR  33101,  3050/xm 
long):  fig.  3,  ext.  lat.;  fig.  4,  ext.  vent,  obi.;  fig.  5,  ext.  ant.  obi.;  fig.  6,  ext.  post.  obi.  Scale  A (75(Vm;  xl8),  figs.  1-6. 


Calocaria  maurae  (2  of  4) 


Stereo-Atlas  of  Ostracod  Shells  14,  46 


Stereo-Atlas  of  Ostracod  Shells  14,  48 


Calocaria  maurae  (4  of  4) 


Stereo-Atlas  of  Ostracod  Shells  14  (13)  49-56  (1987)  Spinohippula  esurialis  (1  of  8) 

595.336.13  (113.312)  (437  : 161.013.49)  : 551.35  + 552.52 


ON  SPINOHIPPULA  ESURIALIS  VANNIER,  KRUTA  & MAREK  gen.  et  sp 

nov. 

by  Jean  Vannier,  Miroslav  Kruta  & Ladislav  Marek 
(University  of  Rennes,  France;  Academy  of  Sciences,  Prague,  Czechoslovakia) 


Derivation  of  name: 
Diagnosis: 

Genus  SPINOHIPPULA  gen.  nov. 

Type-species:  Spinohippula  esurialis  sp.  nov. 

Alluding  to  velar  spines  and  ressemblance  with  species  of  the  tribe  Hippulini.  Gender  feminine. 
Medium  sized  glossomorphitine  (adults  < 1.2mm  long).  Lateral  surface  virtually  lacks  lobation:  sulci  only 
expressed  dorsally  as  two  very  poorly  marked  depressions,  presumably  representing  S2  and  S3.  Strong  velum 
extending  from  near  anterior  cardinal  corner  to  posteromedium  or  posterodorsal  part  of  valve  and  bearing  a 
distinctive  coarse  denticulation  along  inner  margin  bordering  a deep  (maximum  depth  ventrally  and 
anteriorly)  fissum-like  laterovelar  furrow.  Dimorphism  mainly  expressed  in  females  by  a broad  crescent-like 
velar  flange  and  a wide  concave  subvelar  area  (dolonal  antrum)  both  ends  of  which  connect  with  lateral 
surface  of  valve.  Inner  velar  spines  converging  towards  middle  of  domicilium  tend  to  reach  the  lateral  surface 
over  the  laterovelar  furrow.  Tecnomorphs  have  narrower  velum  reduced  to  a row  of  radiating  velar  spines, 
with  laterovelar  furrow  more  open  than  in  females;  marginal  sculpture  unknown. 

Remarks: 

The  inclusion  of  Spinohippula  within  the  Glossomorphitinae  (see  R.  Schallreuter.  Palaeontographica  A,  180. 
1983)  is  justified  by  the  occurrence  of  a strong  velar  sculpture  in  both  females  and  tecnomorphs,  and  well 
marked  velar  dimorphism.  The  shape  of  the  velar  flange  in  females  is  its  most  significant  glossomorphitine 
feature,  consisting  of  a massive  adventral  sculpture  (PI.  14,  52.  fig.  2)  high  the  domicilium.  Comparable 
features  are  in  typical  glossomorphitines  such  as  Collibolbina  collis  collis  (Schallreuter,  1964)  (see  R. 

Explanation  of  Plate  14,  50 

Figs.  1-4,  § LV  (holotype,  NM  L26073,  1188/um  long):  fig.  1,  ext.  lat. ; fig.  2,  ext.  vent.  obi.  (tilted  75°):  fig.  3,  ext.  dors.  obi.  (tilted 
45°),  antero-vent.  part  of  the  valve.  Scale  A (300/u.m;  x69),  figs.  1-3;  scale  B (200/am:  xll5),  fig.  4. 

Stereo- Atlas  of  Ostracod  Shells  14,  51  Spinohippula  esurialis  (3  of  8) 


Remarks:  (cont.) 

Schallreuter,  op.  cit.,  1983)  from  the  middle  Ordovician  of  Baltoscandia  or  Gracquina  hispanica  (Born,  1918) 
(see  J.  Vannier,  Palaeontographica  A,  193.  1986)  from  the  Llandeilo  of  France  and  Spain. 

Schallreuter  {op.  cit.,  1983)  divided  the  subfamily  Glossomorphitinae  into  three  tribes  on  the  basis  of 
different  types  of  velar  dimorphism.  Spinohippula  shares  strong  similarities  with  representatives  of  the  tribe 
Hippulini,  especially  Hippula  and  Parahippula.  Although  no  typical  torus  is  observed  (in  addition  to  the  velar 
flange)  in  Spinohippula , the  general  morphology  of  its  adventral  region  is  strikingly  comparable  to  that  of 
Hippula  (subgenera  H.  ( Hippula ) and  H.  (Cetona))  and  Parahippula.  Schematically,  the  shape  (crescent-like 
sculpture),  position  and  nature  (main  adventral  sculpture  with  hollow  spaces  and/or  radiating  structures)  of 
the  velum  (Text-fig.  2)  are  three  important  characteristics  similar  in  Spinohippula  from  the  middle  Ordovician 
of  Czechoslovakia,  Parahippula  from  the  middle  Ordovician  of  United  States,  and  numerous  species  of 
Hippula  from  the  Ordovician  of  Europe  and  North  America  (see  R.  Schallreuter  & M.  Kruta,  N.  Jb.  Paldont. 
(Mil),  8,  1980).  In  Spinohippula  the  row  of  velar  denticulation  (26  spines  in  holotype)  (PI.  14.  50,  fig.  4;  PI. 
14,  52,  fig.  4)  associated  with  a deep  laterovelar  furrow  forms  a semi-open  peripheral  groove  (Text-fig.  la)  at 
the  junction  of  the  lateral,  marginal  and  velar  surfaces.  By  comparison,  H.  (Cetona)  (Text-fig.  lb),  an 
example  of  a typical  unitoral  hippuline,  exhibits  a row  of  short,  flattened  tubule-like  spaces  (=  part  of  torus) 
connected  to  the  velum,  exactly  at  the  same  place  as  the  semi-open  groove  in  Spinohippula.  Moreover, 
openings  of  these  hollows  (13  in  females  of  H.  (C.)  cetona  cetona  = half  the  number  of  velar  spines  in  the 
holotype  of  S.  esurialis)  are  also  impressed  on  the  velar  flange  surface  (cf.  Text-figs,  la  & lb).  Similar 
comparisons  could  also  be  attempted  with  H.  ( Hippula ) characterized  by  two  tori  (Text-fig.  2d).  The  velar 
flange  of  Parahippula  (Text-fig.  lc)  is  considered  by  Kraft  (Mem.  geol.  Soc.  Am,  86,  1962)  as  a "hollow  velate 
frill  formed  of  two  layers  continuous  with  the  outer  layer  of  shell  wall’'.  The  interpretation  of  this  “hollow 
structure”  is  problematic,  bearing  in  mind  that  two-layered  structures  frequently  observed  on  silicified 
specimens  (see  D.  J.  Siveter,  Stereo-Atlas  Ostracod  Shells,  12  (10),  pi.  54,  fig.  4)  may  be  the  result  of 
diagenetic  processes.  Nevertheless,  as  stated  by  Kraft,  "the  logical  structure  of  the  carapace  wall”  of 
Parahippula  is  a convincing  argument  for  true  hollow  spaces  within  the  velum  (as  reconstructed  in  Text-fig. 

Explanation  of  Plate  14,  52 

Figs.  1-4,  $ LV  (holotype,  NM  L26073,  1 188/u.m  long):  fig.  1,  ext.  dors.  obi.  (tilted  45°);  fig.  2,  ext.  post.  obi.  (tilted  75°);  fig.  3,  ext 
ant.  obi.  (tilted  75°),  postero-vent.  part  of  the  valve;  fig.  4,  ext.  post.  obi.  (tilted  55°).  antero-vent.  part  of  the  valve. 
Scale  A (300/u.m;  x69),  figs.  1,  2;  scale  B (200/u.m;  x 115),  figs.  3,  4. 


Stereo-Atlas  of  Ostracod  Shells  14,  50 


Spinohippula  esurialis  (2  of  8) 


Stereo-Atlas  of  Ostracod  Shells  14,  52 


Spinohippula  esurialis  (4  of  8) 


Stereo-Atias  of  Ostracod  Shells  14,  53  Spinohippula  esurialis  (5  of  8) 

Remarks:  (cont.)  lc).  In  this  case:  1)  the  hollow  spaces  (13  in  females;  Text-fig.  2c)  within  the  velar  flange  of  Parahippula , and 
2)  its  deep  laterovelar  furrow  showing  12  secondary  radiating  tiny  furrows  on  the  velar  flange,  may  represent 
homologous  structures  of  the  13  toral  hollows  of  H.  (Cetona)  (Text-fig.  2b)  and  the  semi-open  laterovelar 
groove  of  Spinohippula  (Text-fig.  2a)  respectively. 


Text-fig.  1.  Reconstructions  of  the  adventral  sculpture  in  three  genera  of  the  tribe  Hippulini  Schallreuter,  1983:  A,  Spinohippula 
gen.  nov.;  B,  Hippula-,  C,  Parahippula.  All  views  represent  medioventral  cross-sections  of  valves  (see  Text-fig.  2).  d = dolonal 
antrum;  do  = domicilium;  If  = laterovelar  furrow;  Is  = lateral  surface;  ms  = marginal  sculpture  (row  of  spines);  t = torus;  v = velar 
flange;  x = probable  hollows  within  the  velar  flange. 

Spinohippula  esurialis  sp.  nov. 

National  Museum,  Prague  (NM),  Czechoslovakia,  coll.  no.  L26073;  9 LV. 

[Paratypes:  NM,  Prague,  coll.  nos.  L26074,  tecnomorph  RV;  L26075.  9 TV].  Casts  of  the  holotype 
and  paratypes  are  in  the  Institute  of  Geology,  University  of  Rennes,  France. 

Ejpovice  (borehole),  10km  E of  Plzen,  WSW  of  Prague,  Bohemia,  Czechoslovakia;  approx,  lat.  49°  47'N. 
long.  13°  38'E.  Sandstones,  Skalka  quartzite  Dobrotiva  (Llandeilo  ?)  ‘series’,  Ordovician. 

Latin,  esurialis , hungry;  referring  to  the  teeth-like  velar  spines. 


Holotype: 

Type  locality: 
Derivation  of  name: 


Explanation  of  Plate  14,  54 

Figs.  1-3,  tecnomorph  RV  (paratype,  NM  L26074,  838/Atn  long):  fig.  1,  ext.  lat.;  fig.  2,  ext.  vent.  obi.  (tilted  45°);  fig.  3,  ext.  post.  obi., 
part  of  the  valve.  Scale  A (300/u.m;  x93),  figs.  1,  2;  scale  B (200/u.m;  xll5),  fig.  3. 


Stereo-Atlas  of  Ostracod  Shells  14,  55 


Spinohippula  esurialis  (7  of  8) 


Text-fig.  2.  Three  genera  of  the  tribe  Hippulini  Schallreuter,  1983.  All  lateral  views  of  female  right  valves.  A,  Spinohippula  esurialis 
gen.  et  sp.  nov.,  from  the  Dobrotiva  series  (Llandeilo  ?)  of  Czechoslovakia,  approximately  x95.  B.  Hippula  (Cetona)  cetona  cetona 
(Schallreuter,  1964),  from  Backsteinkalk  erratic  boulders  of  northern  Germany,  middle  Ordovician,  approximately  x80  (after 
Schallreuter  1983,  op.  cit.  pi.  3,  fig.  1).  C,  Parahippula  ventrospina  (Kraft,  1962),  from  the  middle  Ordovician  of  Virginia,  United 
States,  approximately  x65  (after  Kraft  1962,  op.  cit..  pi.  12,  fig.  5).  D.  Hippula  (Hippula)  latonoda  (Schallreuter,  1964),  from  the 
Upper  Viru  series  (Caradoc)  of  Baltoscandia,  approximately  xlOO  (after  Schallreuter  1983,  op.  cit.,  pi.  5,  fig.  1). 

Figured  specimens:  National  Museum,  Prague  (NM),  Czechoslovakia,  coll.  nos.  L26073  (holotype,  9 LV:  Pi.  14,  50,  figs.  1-4;  PI. 

14,  52,  figs.  1-4),  L26074  (paratype,  tecnomorph  RV:  PI.  14,  54,  figs.  1-3),  L26075  (paratype,  9 LV:  PI.  14, 
56,  figs.  1-3).  Silicone  rubber  casts  of  topotype  specimens. 

As  for  the  genus.  Monotypic. 

The  laterovelar  furrow  represents  a major  concavity,  widely  extended  ventrally,  but  not  connected  to  the 
domiciliar  cavity  and  protected  from  the  outside  by  a row  of  spines;  it  could  be  interpreted  as  an  external 
botulus-like  brood  concavity.  More  likely,  this  groove  is  homologous  to  a cavum  (see  R.  Schallreuter  in  R. 
Maddocks  (Ed.),  Proc.  8th  Int.  Symp.  on  Ostracoda,  Houston,  Texas , 1983)  or  a fissum.  Some  tvaerenellids 
exhibit  an  arcuate  cavum  which  tends  to  be  closed  by  spines  in  the  same  way  as  the  laterovelar  furrow  of  5. 
esurialis.  Huckea  huckea  (see  R.  Schallreuter.  Palaeontographica  A,  149,  pi.  9,  figs.  1-4,  1975)  shows  a ventral 
fissum  positioned  similarly  to  the  furrow  in  S.  esurialis.  The  exact  function  of  the  cavum  (buoyancy  control?) 
or  fissum  is  still  unknown  but  might  represent  an  attempt  to  lighten  the  shell. 

At  present  known  only  from  type  locality. 

To  the  Humboldt  Foundation  (Bonn)  for  my  Research  Fellowship  at  Hamburg  University. 


Diagnosis: 

Remarks: 


Distribution: 
Ac  know  l edgem  ents: 


Explanation  of  Plate  14,  56 

Figs.  1-3,  9 LV  (paratype,  NM  L26075,  1107/Am  long);  fig.  1,  ext.  lat.;  fig.  2,  ext.  dors,  obi.,  postero-vent.  part;  fig.  3,  ext.  post,  obi., 
medio-vent.  part.  Scale  A (300/Am;  x76),  fig.  1;  scale  B (200/Am;  xll5),  fig.  2;  scale  C (100/Am;  x250),  fig.  3. 


Stereo-Atlas  of  Ostracod  Shells  14,  54 


Spinohippula  esurialis  (6  of  8) 


Stereo-Atlas  of  Ostracod  Shells  14,  56 


Spinohippula  esurialis  (8  of  8) 


Stereo-Atlas  of  Ostracod  Shells  14  (14)  57-64  (1987) 
595.336.11  (113.331)  (481  : 161.010.59)  551.35  + 552.54 


Beyrichia  siveleri  ( 1 of  8) 


ON  BEYRICHIA  (SAGENABEYRICHIA)  SIVETERI  POLLICOT 

subgen.  et  sp.  nov. 

by  Paul  D.  Pollicott 
(University  of  Leicester,  England) 


Derivation  of  name: 
Diagnosis: 


Remarks: 


Subgenus  BEYRICHIA  ( SAGENABEYRICHIA ) subgen.  nov. 

Type-species:  Beyrichia  (Sagenabeyrichia)  siveteri  sp.lnov. 

Latin  sagena , fish-net;  alluding  to  the  reticulate  ornament  of  the  lobes  + the  genus  Beyrichia. 
Beyrichia  with  reticulo-tuberculate  lobal  ornament.  Crumina  elongate  and  relatively  well 
assimilated  with  lobal  area.  Syllobium  weakly  cuspidate;  anterior  cusp  slightly  more  prominant. 
posterior  often  lacking.  Syllobial  groove  low  and  often  above  a well  developed  callus.  Zygal  arch 
lacking. 

The  lobal  reticulation  of  B.  ( Sagenabeyrichia ) is  unique  within  Beyrichia.  Moreover,  the 
occurrence  of  reticulation  in  an  otherwise  typical  beyrichiine  species  has  significance  for 
beyrichiacean  phyllogeny,  particularly  in  the  relationship  between  amphitoxotidines  and 
beyrichiines.  Henningsmoen  ( Geol . Foren.  Stockh.  Forh.,  86,  387-9,  1965)  thought  that 
amphitoxotidines,  with  their  typically  tubulose  velar  frill,  evolved  from  beyrichiines  ( Beyrichia 
subgenera).  In  contrast,  Martinsson  (Bull.  geol.  Instn.  Univ.  Uppsala,  42.  56.  1963)  thought  that  a 
stabilized  surface  reticulation  within  the  amphitoxotidines  was  entirely  foreign  to  typical 
beyrichiines  (although  reticulation  is  known  in  atypical  Beyrichiidae  such  as  Bingeria:  see  A. 
Martinsson  Bull.  geol.  Instn.  Univ.  Uppsala.,  41,  1962),  a subfamily  which,  furthermore,  he 

Explanation  of  Plate  14,  58 

Fig.  1-3,  cf  RV  (PMO  116.231,  2.00  mm  long):  fig.  1,  ext.  lat. ; fig.  2,  ext.  vent.;  fig.  3.  ext.  vent.  obi.  Figs.  4,  5,  cf  LV  (PMO  116.232. 

1.32  mm  long):  fig.  4,  ext.  dors,  obi.;  fig.  5,  ext.  lat. 

Scale  A (370  /xm;  x 28),  figs.  1-3;  scale  B (260  gm;  x 40),  figs,  4,  5. 


Stereo-Atlas  of  Ostracod  Shells  14,  59 


Beyrichia  siveteri  (3  of  8) 


1954 


Remarks:  (cont.)  considered  more  ‘advanced’  by  lacking  a tubulose  velum.  Henningsmoen  (op.  cit.)  thought  that 
reticulation  in  the  beyrichiines  was  an  undeveloped  possibility  and.  if  found,  its  occurrence  would 
indicate  a possible  beyrichiine  derivation  for  the  amphitoxotodines.  The  lobal  reticulation  of 
Beyrichia  (Sagenabeyrichia)  supports  his  idea. 

B.  (Sagenabeyrichia)  further  differs  from  many  typical  B.  (Beyrichia)  species  by  its  better 
assimilated  crumina,  a feature  which  it  has  in  common  with  species  of  B.  (Simplicibeyrichia) , 
especially  B.  (S.)  callifera  and  B.  (S.)  duplicicalcarata  (both  Martinsson  op.  cit.,  1962).  B. 
(Sagenabeyrichia)  differs  markedly  from  B.  (S.)  globifera  Martinsson,  1962  by  its  reticulation,  lack 
of  a calcarine  spine,  its  often  well  developed  syllobial  groove/callus  and  in  having  a long,  better 
defined  preadductorial  sulcus. 

Beyrichia  (Sagenabeyrichia)  siveteri  sp.  nov. 

Beyrichia  ( Beyrichia ) cf.  kloedeni  McCoy  1846;  G.  Henningsmoen,  Norsk,  geol.  Tidsskr..  34,  40-43  (pars),  pi.  2,  fig.  7,  10-18, 
pi.  3,  figs.  2-7;  ? pi.  2,  fig.  9. 

Holotype:  Paleontologisk  Museum,  Oslo,  Norway,  PMO  116.233;  9 RV  (broken  posteriorly). 

Coastal  section,  southern  tip  of  Kommerspya  (east  side),  Holmestrand,  Norway.  Steinsfjorden 
Formation,  ‘9c|T  of  Kiaer  (Skr.  Vidensk.  Selsk.  Kristiania  I Mat.  - Naturv.  Kl.  1906  II,  596  pp.); 
Wenlock  Series,  Silurian.  Approx,  lat.  59°  32'N,  long.  10°  18'E. 

After  Dr.  David  J.  Siveter,  University  of  Leicester,  England. 

Paleontologisk  Museum,  Oslo,  nos.  PMO  116.231  (cf  RV:  PI.  14,  58,  figs.  1.  2,  3),  PMO  116.232 
(Cf  LV:  PL  14,  58,  figs,  4,  5,  PI.  14,  62,  fig.  1),  PMO  116.233  ($  RV:  PI.  14,  60.  fig  1)  PMO  116.234 
(9  RV:  PI.  14,  60,  figs.  2,  3).  PMO  116.235  (9  LV:  PI.  14.  60,  fig,  4,  5),  PMO  116.236  (cf  LV:  PI. 
14,  62,  fig  2,  5),  PMO  116.237  (cf  LV:  PI.  14,  62,  fig.  3),  PMO  116.238  (cf  LV:  PI.  14,  62,  fig,  4), 
PMO  116.239  (Cf  LV:  PI.  14,  64,  fig.  1),  PMO  116.240  (cf  LV:  PI.  14,  64,  fig.  2),  PMO  116.241  (cf 
RV:  PI.  14,  64,  fig.  3). 


Type  locality: 


Derivation  of  name: 
Figured  specimens: 


Explanation  of  Plate  14,  60 

Fig.  1,  9 RV,  ext.  lat.  (holotype  PMO  116.233,  2.00  mm  long).  Figs.  2,  3,  9 RV  (PMO  116.234,  2.50  mm  long):  fig.  2,  ext.  vent.;  fig. 

3,  ext.  vent,  detail  of  crumina.  Figs.  4,  5,  9 EV  (PMO  116.235,  2.48  mm  long):  fig.  4,  ext.  vent,  obi.;  fig.  5,  ext.  lat. 
Scale  A (390  /x m;  x 25),  fig.  1;  scale  B (286  /xm;  x 35),  fig.  3;  scale  C (470  /xm;  x 22),  figs.  2,  4,  5. 


Stereo- Atlas  of  Ostracod  Shells  14,  58 


Beyrichia  siveteri  (2  of  8) 


Stereo-Atlas  of  Ostracod  Shells  14,  60 


Beyrichia  siveteri  (4  of  8) 


Stereo-Atlas  of  Ostracod  Shells  14.  61 


Beyrichia  siveteri  (5  of  8) 


Figured  specimens: 
(com.) 

Diagnosis: 

Remarks: 


Distribution: 


All  figured  specimens  are  from  the  Steinsfjorden  Formation  (9c),  Sjorvoll,  Ringerike,  except  for 
PMO  116.233  (holotype)  and  PMO  116.238,  which  are  from  the  type  horizon  and  locality.  All 
specimens  are  prepared  by  mechanical  preparation  techniques  from  limestone  slabs. 

As  for  the  subgenus.  B.  (Sagenabeyrichia)  is  monotypic. 

B.  (S.)  siveteri  exhibits  wide  variation  in  both  lobal  reticulation  and  tuberculation.  Most  valves  are 
reticulate  over  the  entire  lobal  area,  but  in  a few  specimens,  reticulation  is  lacking  on  the  anterior 
lobe  (possibly  a feature  of  preservation?).  Tuberculation  varies  from  forms  with  extensive  cover 
(mostly  adults)  to  those  in  which  it  is  lacking  (small  tecnomorphs).  Reticulation  is  relatively 
smaller  in  larger  forms,  and  tubercles  are  commonly  restricted  to  a supra-velar  field  (PI.  14.  58. 
figs.  1,  5). 

Size  variation  of  female  adults  is  common  within  a single  sample  (see  Text-fig.  1).  This  is 
thought  to  reflect  mixed  populations  (chronodemes  and/or  ecodemes)  rather  than  a possible  case 
of  precocious  dimorphism  (unknown  in  Beyrichiacea). 

The  Wenlock  Series,  Silurian  of  Norway.  Collected  from  localities  in  the  Steinsfjorden  Formation 
(see  Worsley,  D.  (ed.),  Nor.  geol.  unders.  384,  1982)  at  Ringerike  (9b-9e  of  Kiaer,  op.  cit.)  and 
Holmestrand  (9b-9c  of  Kiaer,  op.  cit.). 


Explanation  of  Plate  14,  62 

Fig.  1,  cf  LV,  reticulation  on  syllobium  (PMO  116.232,  1.32  mm  long).  Figs.  2,  5.  cf  RV  (PMO  116.236.  2.32  mm  long):  fig.  2.  ext. 
lat . ; fig.  5,  reticulation  and  tuberculation  on  syllobium.  Fig.  3.  Cf  LV.  ext.  lat.  (PMO  116.237,  2.48  mm  long).  Fig.  4,  cf  LV.  ext. 
lat.  (PMO  116.238,  1.20  mm  long). 

Scale  A (21  /urn;  x 460),  fig.  1;  scale  B (455  /um;  x 23),  figs.  2,  3;  scale  C (230  /urn;  x 40).  fig.  4;  scale  D (62  /urn;  x 150).  fig.  5. 


Stereo-Atlas  of  Ostracod  Shells  14,  63  Beyrichia  siveteri  (7  of  8) 


All  specimens  from  a 2cm  band  in  9cJ.  Wenlock  Series. 
Kommersaya,  Holmestrand. 


.♦V 


• • • 


• % • 


. .*r 

• % 


_l . I , 1 , L_ 


Tecnomorphs  (83  specimens). 
Females  (4  specimens). 

, I I I 


600  800  1000  1200  1400  1600  1800  2000  2200  2400 

Hinge  length  Cum) 


Text-fig.  1.  Size  variation  within  B.  (Sagenabeyrichia)  siveteri  from  the  Steinsfjorden  Formation  (9c  of  Kiaer  op.  cit.),  Wenlock  Series 
at  Kommers0ya,  Ffolmestrand,  Norway. 


Explanation  of  Plate  14,  64 

Fig.  1,  cf  LV,  ext.  lat.  (PMO  116.239,  2.72  mm.  long).  Fig.  2,  cf  LV,  ext.  lat.  (PMO  116.240.  2.68  mm.  long).  Fig.  3 Cf  RV,  ext.  lat. 

(PMO  116.241,  2.68  mm.  long). 

Scale  A (545  /um;  x 18),  figs.  1-3. 


Beyrichia  siveteri  (6  of  8) 


Stereo-Atlas  of  Ostracod  Shells  14,  62 


Stereo-Atlas  of  Ostracod  Shells  14,  64 


Beyrichia  siveteri  (8  of  8) 


Stereo-Atlas  ofOstracod  Shells  14  (15)  65-68  (1987) 
595.337.14  (119.9)  (415  : 162.011.51)  : 551.351 


Bythocythere  intermedia  ( 1 of  4) 


ON  BYTHOCYTHERE  INTERMEDIA  ELOFSON 

by  David  J.  Horne 

(Geology  Department,  City  of  London  Polytechnic) 


Type  specimens: 
Type  locality: 

Figured  specimens: 


Bythocythere  intermedia  Elofson,  1938 

1868  Bythocythere  constricta  Sars;  G.  S.  Brady,  Trans.  Linn.  Soc.  Lond. , 26,  (pars),  451-452,  pi.  35.  figs.  48-52  only  (non  pi.  35.  fig. 
47)  (non  Sars,  1866). 

1938  Bythocythere  intermedia  sp.  nov.  O.  Elofson,  Ark.  Zool.,  30A,  10,  text-figs.  14-21. 

1983  Bythocythere  intermedia  Elofson;  J.  Athersuch.  D.  J.  Horne  & J.  E.  Whittaker,  J.  micropalaeontol. , 2,  72-73,  text-figs.  1,  2, 
3a-g,  4r-t,  5b;  pi.  2,  figs.  1-4. 

The  whereabouts  of  Elofson’s  type  material  is  not  known. 

The  Mittskaren,  outside  the  mouth  of  Gullmar  Fjord,  W.  Sweden,  approx,  lat.  58°15'N,  long. 
11°30'E;  Recent,  marine,  sublittoral. 

British  Museum  (Nat.  Hist.)  nos.  1982.345  (cf  LV;  PI.  14,  68,  fig.  1;  copulatory  appendage: 
Text-fig.  1),  1982.346  ($  LV:  PI.  14,  66,  fig.  2;  RV:  PI.  14,  66,  fig.  3),  1982.347  (cf  LV:  PI.  14,68. 
figs.  2,  3),  1982.348  (cf  LV : PI.  14,  66,  fig.  1).  All  from  Valentia,  SW  Ireland  (approx,  lat. 
51°55'N,  long.  10°20'W),  taken  from  slides  labelled  “B.  constricta"  in  the  Norman  Collection  at 
the  British  Museum  (Nat.  Hist.);  nos.  1982.345-347  are  from  slide  1900-3-6-379,  no.  1982.348  is 
from  slide  1911.11.8  M3725. 

Diagnosis:  Moderately  large  (750-850/T.m  long)  species  of  Bythocythere ; carapace  moderately  inflated, 

greatest  width  a little  behind  mid-length.  Greatest  height  well  behind  mid-length.  Dorsal  margin 
convex  in  female,  almost  straight  in  male;  ventral  margin  weakly  sinuous  in  both  sexes.  Posterior 
margin  denticulate.  Dorsomedian  sulcus  weak.  Male  copulatory  appendage  with  a relatively  large, 
subtriangular  distal  process. 

Explanation  of  Plate  14,  66 

Fig.  1,  cf  LV,  ext.  lat.  (1982.348,  840^m  long);  figs.  2,  3,  $ (1982.346,  810 /am  long):  fig.  2,  LV,  ext.  lat.;  fig.  3,  RV.  ext.  lat. 

Scale  A (lOO^um;  x80),  figs.  1-3. 


Stereo-Atlas  of  Ostracod  Shells  14,  67 

Remarks: 


Distribution: 


Bythocythere  intermedia  (3  of  4) 

Early  records  of  B.  constricta  Sars  from  British  waters  are  now  believed  to  be  referable  to  either  B. 
intermedia  or  B.  zetlandica  Athersuch,  Horne  & Whittaker,  1983  (see  Horne,  Stereo-Atlas 
Ostracod  Shells , 14,  69-72,  1987).  neither  of  which  possesses  the  deep  median  sulcus  which  is 
characteristic  of  Sars’  species.  B.  zetlandica  has  a smooth  posterior  margin  and  is  less  elongate  with 
a generally  less  rounded  lateral  outline  than  B.  intermedia.  A closely  similar  Miocene  species,  B. 
neerlandica  Kuiper,  1918,  is  less  elongate,  less  tapered  anteriorly,  and  has  a deeper  dorsomedian 
sulcus  than  B.  intermedia. 

Fairly  common  in  sublittoral  marine  waters  around  British  coasts,  the  southern  North  Sea,  S 
Norway  and  Sweden,  and  as  far  south  as  the  Bay  of  Biscay. 


Text-fig.  1 Bythocythere  intermedia , male  copulatory  appendage  (1982.345). 


Explanation  of  Plate  14,  68 

Fig.  1,  cf  LV,  dors.  (1982.345,  820 pm  long);  figs.  2,  3,  cf  LV  (1982.347,  790 p.m  long):  fig.  2,  int.  lat. ; fig.  3,  central  muscle  scar  field. 
Scale  A (100/um;  x80),  figs.  1,  2;  scale  B (50p.m;  x400),  fig.  3. 


Stereo-Atlas  of  Ostracod  Shells  14,  66 


Bythocythere  intermedia  (2  of  4) 


Stereo-Atlas  of  Ostracod  Shells  14,  68 


Bythocythere  intermedia  (4  of  4) 


Stereo- Atlas  of  Ostracod  Shells  14  (16)  69-72  (1987)  Bythocythere  zetlandica  (1  of  4) 

595.337.14  (119.9)  (411  : 162.002.61  + 415  : 162.011.51)  : 551.351 


ON  BYTHOCYTHERE  ZETLANDICA  ATHERSUCH, 
HORNE  & WHITTAKER 


by  David  J.  Horne 

(Geology  Dept,  City  of  London  Polytechnic) 


Bythocythere  zetlandica  Athersuch,  Horne  & Whittaker,  1983 

1868  Bythocythere  constricta  Sars;  G.  S.  Brady,  Trans.  Linn.  Soc.  Land.,  26,  (pars),  451,  pi.  35,  fig.  47  only  ( non  pi.  35,  figs  48-52) 
( non  Sars,  1866). 

1983  Bythocythere  zetlandica  sp.  nov.  J.  Athersuch,  D.  J.  Horne  & J.  E.  Whittaker,  J.  micropalaeontol.,  2,  73,  text-figs  41-n,  5c,  pi. 
2,  figs  5-8. 

Holotype:  British  Museum  (Nat.  Hist.)  no.  1982.350,  9 carapace  and  appendages. 

|Paratype,  no.  1982.351,  cf  carapace  and  appendages.) 

Type  locality:  Unst  Haaf  (fishing  grounds  off  Unst),  Shetland,  approx,  lat.  61°  00'N,  long.  1°  30'W;  Recent, 

marine,  sublittoral. 

Figured  specimens:  British  Museum  (Nat.  Hist.)  nos.  1982.350  (holotype,  9 LV:  PI.  14,  70,  fig.  2;  RV:  PI.  14,  70,  fig. 

3),  1982.351  (paratype,  cf  LV:  PI.  14,  70,  fig.  1),  1982.352  (cf  LV:  PI.  14,  72,  fig.  1;  copulatory 
appendage:  Text-fig.  1),  1982.353  (cf  LV:  PI.  14,  72,  figs  2-3).  All  taken  from  slides  labelled  “ B . 
constricta ” in  the  Norman  Collection  at  the  British  Museum  (Nat.  Hist.):  the  holotype  and 
paratype  are  from  slide  no.  1900-3-6-379;  nos  1982.352  and  1982.353.  both  from  Valentia,  SW 
Ireland  (approx,  lat.  51°  55'N,  long.  10°  20'W),  are  from  slides  1900-3-6-379  and  1911.11.8.  M3725 
respectively. 


Explanation  of  Plate  14,  70 

Fig.  1,  Cf  LV,  ext.  lat.  (paratype,  1982.351,  770  pi m long);  figs.  2,  3.  9 (holotype,  1982.350,  790  jotm  long):  fig.  2.  LV,  ext.  lat.;  fig.  3, 
RV,  ext.  lat. 

Scale  A (100  pun;  x 80),  figs  1-3. 


Stereo- Atlas  of  Ostracod  Shells  14,  71  Bythocythere  zetlandica  (3  of  4) 


Diagnosis: 


Remarks: 


Distribution: 


Moderately  large  (750-800  pm  long)  species  of  Bythocythere ; carapace  strongly  inflated,  greatest 
width  a little  behind  mid-length.  Dorsal  and  ventral  margins  virtually  straight,  converging 
anteriorly,  greatest  height  well  behind  mid-length.  Posterior  margin  smooth.  Dorsomedian  sulcus 
weak.  Distal  process  of  male  copulatory  appendate  relatively  long,  with  a convex  anterior  margin 
and  an  almost  straight  posterior  margin. 

B.  zetlandica  was  formerly  confused  with  B.  constricta  Sars,  which  does  not  live  in  British  waters; 
Sars’  species  has  a characteristically  deep  dorsomedian  sulcus,  and  the  distal  process  of  its  male 
copulatory  appendage  is  more  symmetrical  and  slender  than  that  of  B.  zetlandica.  A similar  NW 
European  species,  B.  intermedia  Elofson,  1938  (see  Horne,  Stereo-Atlas  Ostracod  Shells  14,  65-68, 
1987),  is  more  elongate  than  B.  zetlandica  and  has  a denticulate  posterior  margin  and  a more 
rounded  outline  in  lateral  view. 

A marine  species  found  in  sublittoral  waters  around  British  coasts,  particularly  in  the  north. 


Text-fig.  1 Bythocythere  zetlandica,  male  copulatory  appendage  (1982.352). 


Explanation  of  Plate  14,  72 

Fig.  1,  cf  LV,  dors.  (1982.352,  800  pun  long);  figs  2,  3 cf  LV  (1982.353,  780  pun  long):  fig.  2,  int.  lat.;  fig.  3,  central  muscle  scar  field. 
Scale  A (100  pun;  X 80),  figs  1,  2;  scale  B (50  pun;  X 400),  fig.  3. 


Stereo-Atlas  of  Ostracod  Shells  14,  70 


Bythocythere  zetlandica  (2  of  4) 


Bythocythere  zetlandica  (4  of  4) 


Stereo-Atlas  of  Ostracod  Shells  14,  72 


Stereo-Atlas  of  Ostracod  Shells:  Vol.  14,  Part  1 

CONTENTS 

On  Cathaycythere  reticulata  Whatley  & Zhao  gen.  et  sp.  nov.;  by  R.  C. 
Whatley  & Zhao  Quanhong 

On  Sinocythere  sinensis  Hou;  by  R.  C.  Whatley  & Zhao  Quanhong 
On  Albileberis  sinensis  Hou;  by  Zhao  Quanhong  & R.  C.  Whatley 
On  Sinocytheridea  impressa  (Brady);  by  Zhao  Quanhong  & R.  C.  Whatley 
On  Pterygocythereis  vannieuwenhuisei  Brouwers  sp.  nov.;  by  E.  M. 
Brouwers 

On  Muellerina  hazeli  Coles  & Cronin  sp.  nov.;  by  G.  P.  Coles  & T.  M. 
Cronin 

On  Healdianella?  aremorica  Crasquin  sp.  nov.;  by  S.  Crasquin 
On  Maghrebeis  tuberculata  Majoran  gen.  et  sp.  nov.;  by  S.  Majoran 
On  Howeina  camptocytheroidea  Hanai;  by  N.  Ikeya  & E.  Compton - 
Gooding 

On  Spinoleberis  eximia  (Bosquet);  by  J.  F.  Babinot  & J.  P.  Colin 
On  Kovalevskiella  caudata  (Lutz);  by  P.  Carbonel,  J.  P.  Colin  & L.  Londeix 
On  Calocaria  maurae  Vannier  gen.  et  sp.  nov.;  by  J.  Vannier 
On  Spinohippula  esurialis  Vannier,  Kruta  & Marek  gen.  et  sp.  nov.;  by  J. 
Vannier,  M.  Kruta  & L.  Marek 

On  Beyrichia  (Sagenabeyrichia)  siveteri  Pollicott  subgen.  et  sp.  nov.;  by 
P.  D.  Pollicott 

On  Bythocythere  intermedia  Elofson;  by  D.  J.  Horne 
On  Bythocythere  zetlandica  Athersuch,  Horne  & Whittaker;  by  D.  J.  Horne 

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Individual  subscription  £22.00  or  US  $50.00  for  2 parts  (post  free) 

Price  per  Part:  £22.00  or  US  $50.00 
Institutional  subscription  £45.00  or  US  $80.00  for  2 parts  (post  free) 

Price  per  Part:  £45.00  or  US  $80.00 

Back  volumes:  Vol.  1 (4  Parts):  £20.00;  price  per  Part:  £5.00 
Vol.  2 (4  Parts):  £28.00;  price  per  Part:  £7.00 

Vol.  3 (2  Parts):  £24.00;  price  per  Part:  £12.00 

Vol.  4 (2  Parts):  £30.00;  price  per  Part:  £15.00 

Vol.  5 (2  Parts):  £32.00;  price  per  Part:  £16.00 

Vol.  6 (2  Parts):  £40.00;  price  per  Part:  £20.00 

Vol.  7 (2  Parts):  £40.00;  price  per  Part:  £20.00 

Vol.  8 (2  Parts):  £60.00;  price  per  Part:  £30.00 

Vol.  9 (2  Parts):  £60.00;  price  per  Part:  £30.00 

Vol.  10  (2  Parts):  £60.00;  price  per  Part:  £30.00 

Vol.  11  (2  Parts):  £60.00;  price  per  Part:  £30.00 

Vol.  12  (2  Parts):  £60.00;  price  per  Part:  £30.00 

Vol.  13  (2  Parts):  £60.00;  price  per  Part:  £30.00 

Postage  extra  in  sales  of  all  back  Parts 
No  trade  discount  is  allowed  on  the  subscription  rate 

Orders  should  be  addressed  to:  Dr  R.  C.  Whatley, 

Department  of  Geology, 

University  College  of  Wales, 

Aberystwyth,  Dyfed. 

Cheques  should  be  made  payable  to  B.M.S.  (Stereo-Atlas  Account) 

SPECIAL  OFFER 


14  (1) 

1-  4 

14  (2) 

5-  8 

14  (3) 

9-12 

14  (4) 

13-16 

14  (5) 

17-20 

14  (6) 

21-24 

14  (7) 

25-28 

14  (8) 

29-32 

14  (9) 

33-36 

14  (10) 

37-40 

14  (11) 

41-44 

14  (12) 

45-48 

14  (13) 

49-56 

14  (14) 

57-64 

14(15) 

65-68 

14  (16) 

69-72 

50%  off  all  back  part  prices  if 
you  become  a subscriber  to  the  Atlas