. es ee mecca ne ial bess oon Bae Ges + am ah ae ey ye hates 8 i. 3 r%; eStats et r ! pesheresest Sant eer Ee react Se weak? im S ie ey ts 7 Breet ; specaets Messtecnyeeestane : : : - : re s < Rees > Hay ame : : ; state : : “per! : we eotyti tet eterer ts 2 td . * $ 42t28. beter staat its ix 7, He } i oe : Rees eepekectigs ay fal bhi yes aslesteni ts tory itt: th a4 Boo) sat ] ae aa) e ao 4 ‘ ra es ’ Set Weta ets - se Seererenchiaese prshgnagatst that Sete bs teinaga Ve CARDIGAN BAY RECENT FORAMINIFERA (CRUISES OF THE R. V. ANTUR, 1962-1964) J. R. HAYNES BULLETIN OF THE BRITISH MUSEUM (NATURAL HISTORY) ZOOLOGY SUPPLEMENT 4 | LONDON : 1973 CARDIGAN BAY RECENT FORAMINIFERA (CRUISES OF THE R. V. ANTUR, 1962-1964) BY JOHN ROLAND HAYNES with assistance from TERENCE DAVID ADAMS, KEITH ATKINSON, EMMANUEL ABIODUN FAYOSE, DREW HAMAN, KEITH HAVARD JAMES, JOAN ANNE JOHNSON & JOHN SCOTT. 33 Plates, 47 Text figures BULLETIN OF THE BRITISH MUSEUM (NATURAL HISTORY) ZOOLOGY SUPPLEMENT 4 LONDON : 1973 THE BULLETIN OF THE BRITISH MUSEUM (NATURAL HISTORY), tnstituted im 1949, 15 issued in five series, corresponding to the Departments of the Museum, and an Historical serves. Parts will appear at irregular intervals as they become veady. Volumes will contain about three or four hundred pages, and will not necessarily be completed within one calendar ‘year. In 1965 a separate supplementary series of longer papers was instituted, numbered serially for each Department. This paper 1s Supplement 4 of the Zoological series. The abbreviated titles of pertodicals cited follow those of the World List of Scientific Periodicals. World List abbreviation Bull, Br. Mus. nat. Hist. (Zool.) Suppl. © Trustees of the British Museum (Natural History), 1973 TRUSTEES OF THE BRITISH MUSEUM (NATURAL Ei Sai @ Ry.) cased - : Issued 12 February, 1973 Price £10.80 CARDIGAN BAY RECENT FORAMINIFERA (CRUISES OF THE R. V. ANTUR, 1962-1964) By J. R. HAYNES with assistance from fh, D. ADAMS;.K: ATKINSON, E..A. FAYOSE, Ds HAMAN, KH JAMES; J; A] JOHNSON &*f. SCOTT CONTENTS Page I. INTRODUCTION , ; : ; : ‘ é i ' 8 Il. METHODS : : ‘ : 3 : : : ; 10 III. LoOcATION OF MATERIAL . : : : : : : : II IV. ACKNOWLEDGEMENTS é : : : : : : : 1 V. CLASSIFICATION : : ; ‘ ‘ : , : Le VI. SYSTEMATIC DESCRIPTIONS : ; : : : : 14 Family ASTRORHIZIDAE Brady ; ; : : : 14 Genus Halyphysema Bowerbank . ; : : 14 Halyphysema tumanowtczit Bowerbanis : : 14 Genus Hippocrepina Parker : ‘ ; : ; 15 Hippocrepina species A. ‘ : : ‘ 15 Genus Marsipella Norman . ; ; : : 16 Marsipella elongata Norman ; : ; : 16 species A : : : : 17 species B ; : : ‘ : 17 Genus Technitella Norman . : ; : ‘ 17 Technitella tervyense Haynes n. oh : : . 17 Family SACCAMMINIDAE Brady . : : ‘ : 18 Genus Psammosphaera Schultze . : : : : 18 Psammosphaera parva Flint : : : : 18 Genus Lagenammina Rhumbler . : ; : : 19 Lagenammina arenulata (Skinner) A 19 cf. hancocki (Cushman & McCulloch) 20 Genus Hemisphaerammina Loeblich & Tappan : 21 Hemisphaerammina bradyi Loeblich & me : at Family HORMOSINIDAE Haeckel . : ; 22 Genus Reophax Montfort. ‘ 5 : : : 22 Reophax arctica Brady : : : : ; 22 Reophax fustformis (Williamson) : : : 23 moniliforme Siddall ; : ; , 24 Family LITUOLIDAE de Blainville . : : : 5 25 Genus Ammobaculites Cushman . i : : es. of 25 Ammobaculites balkwilli Haynes n. sp. : : 25 Genus Haplophragmoides Cushman ‘ : : . 27, J. R. HAYNES Page Haplophvagmoides wilbertt Anderson . : : ZT, species A : : ; ; 28 Genus Cribrostomoides Cushman . ; : : : P40) Cribrostomoides jeffreysu (Williamson) . : : 29 Family TEXTULARIIDAE Ehrenberg : : 3 ; 31 Genus Spiroplectammina Cushman : : : : 31 Spiroplectammina eavlandi (Parker) . : ; 31 wrightit (Silvestri) . : 32 Family TROCHAMMINIDAE Schwager . : 3 : 34 Genus Trochammina Parker & Jones . : : 34 Trochammina astrifica (Rhumbler) . : 3 34 haynest Atkinson . 35 globigeriniformis var. _ pygmaca Hom lund: =: : : : ‘ 36 inflata (Montagu) . : : ; 37 intermedia? Rhumbler . ; ; 39 ochvacea (Williamson) . : : 40 Genus Jadammina Bartenstein & Brand : : 41 Jadammina macrescens (Brady) . ; : : AI Genus Remaneica Rhumbler ‘ : : 5 43 Remaneica helgolandica pricier : : 43 Family ATAXOPHRAGMIIDAE Schwager : : ; 44 Genus Eggerelloides Haynes n. gen. : ‘ : : 44 Eggerelloides scabyum (Williamson) . 5 : 44 Genus Textilina Norvang . ; : : : : 47 Textilina bocki (Hoglund) . : 5 : 47 Family FISCHERINIDAE Millett. : d 48 Genus Cyclogyva Wood ; : 48 Cyclogyrva selseyensis (Elerou Allen & eae ; 48 Family NUBECULARIDAE Jones . 5 ; : 50 Genus Spirvopthalmidium Cushman 5 ; : 50 Spivopthalmidium acutimargo var. emaciatum Haynes n. var. . : 3 : : : 50 Family MILIOLIDAE Ehrenberg : : : ‘ 3 52 Genus Massilina Schlumberger . : ; : 52 Massilina carinata (Fornasini) — . : : : 52 secans (d’Orbigny) . : : : 53 Genus Miliammina Heron-Allen & Earland . : 54 Miliammina fusca (Brady) 2 ; : : 54 Genus Miliolinella Wiesner . ; é , ; 56 Miliolinella subrotunda iitonraen : oie 56 subrotunda pateorid var. . ; : ; ef 57 Genus Pyrgo Defrance : . . . 59 Pyrgo carinata (d’ Orbigny): : ‘ : d 59 cf. constricta Costa . : : : : 60 wiliamsoni (Silvestri) E : : 6I species A : ; ‘ 5 : 5 62 species B ; é E : : 63 Genus Quingueloculina (d’ Orbea) : si : : 63 Quinqueloculina aspera d’Orbigny ; : : 63 auberiana var. A : ; : 65 var. B : : 66 bicornis (Walker & Jacon) : 3 67 CARDIGAN BAY RECENT FORAMINIFERA cf. chavensis Heron-Allen & Ear- land cf. cliarensis var. A ; cf. duthiersi (Schlumberger) . intrvicata Terquem ; lata Terquem meditervanensis Le ec & Le Calvez cf. rugosa d’Orbigny seminulum (Linnaeus) Genus Scutulovis Loeblich & pee Scutuloris species A . Genus Sigmoilopsis Finlay Sigmotlopsis moyt Atkinson Genus Spiroloculina d’Orbigny . Spivoloculina depressa Q’ Crinaawe Genus Tviloculina d’Orbigny : Triloculina trigonula (Lamarck) . tvihedva Loeblich & Pappa Family NODOSARIIDAE Ehrenberg. Genus Dentalina Risso Dentalina cf. ES Reyne Taemeen Genus Lagena Walker & Jacob Lagena clavata (d’Orbigny) doveyensis Haynes n. sp. hibernica Haynes n. sp. . laevis (Montagu) pacifica Sidebottom periucida (Montagu) semistyviata (Williamson) spicata (Cushman & McCulloch) cf. striata (d’Orbigny) substriata Williamson sulcata (Walker & Jacob) sulcata interrupta (Williamson) sulcata torquiformis eee Havahas. species A Family POLYMORPHINIDAE d’Orbigny . Genus Fissuvina Reuss Fissurina elliptica (cise) lucida (Williamson) marginata (Walker & Boys) species PAs : : species B . Genus Globulina d’Orbigny . Globulina cf. inaequalis Reuss Genus Guttulina d’Orbigny . Guttulina (?Laryngosigma) eaeise Haynes n. oy Genus Laryngosigma Loeblich & Tappan Laryngosigma hyalascidia Loeblich & pea lactea (Walker & Jacob) lactea concava (Williamson) Genus Oolina d’Orbigny J. R. HAYNES Oolina borealis Loeblich & Tappan heronallent Haynes n. sp. hexagona (Williamson) laevigata d’Orbigny. lineata (Williamson) squamosa (Montagu) williamsont (Alcock) Genus Pseudopolymorphina Cushman & Ozawa Pseudopolymorphina cf. novangliae (Cushman) suboblonga Cushman & Ozawa Family TURRILINIDAE Cushman Genus Buliminella Cushman Buliminella borealis Haynes n. oP Family BULIMINIDAE Jones . Genus Bulimina d’Orbigny . Bulimina elongata d’ Orbigny elongata lesleyae Atkinson elongata subulata Cushman & Baker gibba Fornasini . : marginata d’Orbigny . Genus Stainfortiia Hofker . : ; ; Stainforthia concava var. (Feyling-Hanssen) ‘Stainforthia’ fusiformis (Williamson) . species A Family UVIGERINIDAE Haeckel Genus Trifavina Cushman ; : Trifavina angulosa (Williamson) . Family BOLIVINITIDAE Cushman . Genus Bolivina d’Orbigny Bohvina britanmica Macfadyen : inflata Heron-Allen & Earland minima Phlieger & Parker cf. minima Phleger & Parker ovdinaria Phleger & Parker pseudoplicata Heron-Allen & Barland pseudopunctata Hoglund spathulata (Williamson) stviatula Cushman superba Emiliani . cf. vadescens Cushman sensu Heslued variabilis (Williamson) . Family SPIRILLINIDAE Reuss Genus Patellina Williamson. Patellina corvrugata Williamson Genus Spivillina Ehrenberg. Spirillina perforata (Schultze) Spirillina species A . ; Genus Turrispirillina Cushman Turrispirillina species A Family DISCORBIDAE Ehrenberg Genus Cancris Montfort . Cancris oblongus (Williamson) Genus Discorbis Lamarck CARDIGAN BAY RECENT. FORAMINIFERA 7 Page Discorbis wright (Brady) . , : : ; 147 Genus Discorbinella Cushman & Martin : : ; 149 Discorbinella species A : : . : 149 Genus fosalina d’Orbigny . : ; ; : : 150 Rosalina anomala Terquem : : : 150 cf. bvadyi (Cushman) . ; : 153 ivegulavis Rhumbler . : : ; 154 millettia (Wright) : : 3 : 155 neopolitana (Hofker) . : : 158 praegert (Heron-Allen & Earland) . : 159 williamsoni (Chapman & Parr) : 4 162 SPeCIes Awan: , : : : 163 Family ASTERIGERINIDAE @’ Orbigny , ; . : 164 Genus Astevrigerinata Bermudez . : : : 164 A sterigevinata mamilla (Williamson) . BS re 164 Family SIPHONINIDAE Cushman . : : : ; 167 Genus Siphonina Reuss : , ; 167 Siphonina georgiana eyes n. sp. : ; : 167 Family EPONIDIDAE Hofker . ; . : . : 168 Genus Eponides Montfort . : ; 168 Eponides vepandus concameratus (Montagu) : : 168 Family CIBICIDIDAE Cushman , . : ; : 171 Genus Cibicides Montfort . : : : I7t Cibicides fletchert Galloway & W eles : : 171 fletcheri sachalinica Vasilenko : : E72 lobatulus (Walker & Jacob) . : : 173 Family PLANORBULINIDAE Schwager : : 77 Genus Planorbulina d’Orbigny ; ‘ 5 ; LGA) Planorbulina distoma Terquem . : ; 177 species A : ; 180 Family GLOBIGERINIDAE Carpenter, Parker & Jones : 180 Genus Biorbulina Blow ; : : : : 180 Biorbulina bilobata (d’ Orbigny) : ‘ 180 Genus Globoquadrina Finlay , : 181 Globoquadrina hexagona (N ntland) : : ; 181 Genus Globorotalia Cushman : ; : 182 Globorotalia inflata (d’Orbigny) . : ; 182 Genus Orbulina d’Orbigny . : : ; : : 184 Orbulina universa d’Orbigny ; i : 184 Family ROTALIIDAE Ehrenberg... ‘ : 184 Genus Ammonia Brunnich . . : ; 184 Ammonia aberdoveyensis Haynes ie Sp! : 184 batavus (Hofker) F 187 limnetes (Todd & eee) . 189 tepida (Cushman) ‘ : ; I9QI Genus buccella Anderson . L : : : 193 Buccella frigida (Cishrian) ; ; ‘ 193 Family CASSIDULINIDAE d’Orbigny ; : ‘ 194 Genus Cassidulina d’Orbigny : : : 194 Cassidulina cf. ventforme fNosvane) 5 : : 194 Family NONIONIDAE Schultze : : ‘ 196 Genus Elphidium Montfort : : : 197 Elphidium asterotuberculatum (Voor {huysen) : 197 3 J. R. HAYNES Page cuvillient Lévy . : : ; } LO exoticum Haynes n. sp. : 3 ; 198 incertum (Williamson) : : ; 199 macellum (Fichtel & Moll) . : ; 201 magellanicum Heron-Allen & Earland . 202 margaritaceum (Cushman) . : 203 selseyense s.1. (Heron-Allen & Farland) s 204 _— waddensis (Voorthuysen) . : 206 williamsont Haynes n. sp. 3 ‘ 207; Genus Nonion Montfort : : : 209 Nonion depressulus (Walker & pee Ne : 209 pauperatum (Balkwill & Wright). : Pato) Genus Nonionella Cushman : : 201 Nonionella auricula Heron- Allen & Barend: : ZU turgida Williamson . ; : 213 turgida var. digitata Nonrane : : 214 species A. : F : : : 215 Genus Protelphidium Haynes ; f : ; : 216 Protelphidium anglicum Murray . : : pe 16) Family UNCERTAIN ; , : : 217, Genus Epistominella hess & Marahasi : : é 217 Epistominella navaensis (Kuwano) : : : 2G VII. SUMMARY AND CONCLUSIONS . F F : : : 5 219 VIII. REFERENCES ; : : : : ; : ; : 22K IX. INDEX TO GENERA, SPECIES AND VARIETIES , : : 3 239 X. ADDENDUM . : : A ; 5 : : : : 244 SI NOE SiS One hundred and sixty five species of foraminifera are described from sediments collected in Cardigan Bay (Wales). These belong to sixty-five genera and twenty-seven families. One genus and twelve species and varieties are renamed or new. This fauna includes most of the abundant shallow water forms on the British List. lL. pI NERODUCiEILON Raison d’étve. Since the publication of ‘Testacea minuta rariora nuperrime detecta in arena littoris Sandvicensis’ by Walker & Boys (1784) upwards of 300 papers have been written concerned at least in part with Recent foraminifera from the seas surrounding the British Isles. However, most of these works contain lists only, and the monograph ‘On the Recent Foraminifera of Great Britain’ by Williamson (1858) is the only comprehensive account, with descriptions as well as illustrations of about go species. This was noted by Earland (1902) in his plea for a new ‘Williamson’, and remains true despite the notable contributions made by Heron- Allen and Earland in their studies of Clare Island (1913b), West of Scotland (1916a) and Plymouth (1930). These works contain figures and descriptions of new species but the other species are only partially illustrated, often by abnormal or unusual specimens, a [Se e ° e e ee e © e ° Be e e jp 8ercsey Is, aor 318 e e 317 se 316 e 573 e ° e °BM13 e e 5 ©BMI4 D) e e e So O e Sos 2 30’ O ‘ e e e : ®BMI15 e e ° 0 e © 2 es e e 4 e e e e e e 0 e e eo 501 $ e ee 521 e e e °BMI6 e e ©BMI7 e e i ee O e e e e e e 6 e e ° e e e 0 e e e 0 + Cardigan e 52° r. _ SAMPLE STATIONS IN CARDIGAN 30’ e e ee fds 494 & 0 5 10 499 4g8 @ Ke e © eo &® A KILOMETRES OO a : e POMETRES | eee ae] e cee N.MILES 0 Ba “9, 5h 7, ° e 559 528 © 8 8 fal, SAMPLE AREA IN RELATION ody te, 738 TO THE BRITISH ISLES 1c e 553 e e e “4% e 555 e eo 5 6 b/ 551 Fal /, : +New Quay ce ~ See ee = co St ieee : ee * eS ners aceralg CARDIGAN BAY RECENT FORAMINIFERA 9 There is thus an obvious need for an up to date taxonomic study of the British Recent foraminifera. This has been made more pressing by the great expansion in distribution studies being made all over the world, largely a consequence of the application of foraminifera to problems of palaeoecology, particularly in the oil industry. Large numbers of foreign workers are thereby faced with the problem of comparing their material with long established but inadequately described British species. Our work in Cardigan Bay has led to the recognition of some 200 foraminiferal taxa of which 165 species and varieties are here described. This includes most of the shallow water forms on the British list and presents an ideal opportunity for their redescription and revision. It is hoped to deal with the remaining deeper water forms in a later publication. Scope of the study. This report is concerned with the taxonomy of the foraminifera and with an attempt, where feasible, to establish their world-wide range. As their detailed distribution and ecologic relationships within Cardigan Bay will be dealt with elsewhere the physical setting will not be described here. For present purposes an adequate summary is given by Moore (1968) who, in a paper on the sediments of Northern Cardigan Bay, includes an account of the bathymetry, circulation and climate. Further details for the southern part of Cardigan Bay are given by Whatley & Wall (1969). Information pertaining particularly to the Dovey Estuary area can be found in Haynes & Dobson (1969). Maternal. The foraminifera have been picked from sediment taken at more than 600 stations made during the years 1962-64 by the research vessel ‘Antur’ (Text-fig. 1). For convenience, only the samples mentioned in the text are num- bered onthe map. Most of the samples were taken in depths of less than 15 fathoms (approximately 30 metres) in the inner bay, with a more widely spaced scatter down to depths of 40 fathoms (approximately 80 metres) in the outer bay. The samples thus represent the upper continental shelf and turbulent zone. They have been supplemented by samples collected along the shore between tide marks during the years 1962-1967, in particular from rock pools such as those at Monks Cave, immediately south of Aberystwyth (Atkinson, 1969) and from the Dovey Estuary and marshes. Maps of the sample stations in the Dovey Estuary including the Clettwr Transect and the location of boreholes into the Holocene sediments are given in Adams & Haynes (1965) and Haynes & Dobson (1969). Also shown in Text-fig. 1 are the locations of five small gravity cores taken by the R.V. ‘Shackleton’ for the British Museum and used in our study, B.M. Cores 13-17. Previous work. This study is a contribution to the Cardigan Bay-—Irish Sea Research Project of the Geology Department, University College of Wales, Aberyst- wyth. The Project was instituted in 1962 and is concerned with the investigation of the geological history of the area, present day sedimentation, faunas and their ecological relationships. Some 2000 sediment samples have now been collected in Cardigan Bay and the Southern Irish Sea (including St Georges Channel). A -number of foraminiferal investigations have been carried out under the direction of Dr J. R. Haynes and the results presented as dissertations for the Ph.D. and M.Sc. degrees and the College Diploma in Micropalaeontology. These works which J. R. HAYNES are available on inter-library loan are as follows in order of date: Adams (1963) ; James (1965); Johnson (1965); Fayose (1965); Haman (1966a); Scott (1966) ; Atkinson (1967). In addition the following papers on different aspects of foramini- feral distribution and taxonomy have appeared: Wood, Adams & Haynes (1963) ; Haynes (1964, 1965); Adams & Haynes! (1965); Adams, Haynes & Walker (1965); Haman (1966b, 1967, 1969) ; Atkinson (1968, 1969) ; Haynes & Dobson (19609). There had been no previous work on the foraminifera in Cardigan Bay. At a very early stage in these investigations we faced the difficulty of finding correct names for many of the species. In order to speed the studies of distribution we decided to follow ‘accepted British usage’ until such times as we had accumulated sufficient good material to justify tackling the knotty nomenclatural problems we knew pected. We were helped at the outset in this by the advantage of having to hand the unpublished thesis of Dr T. J. Harris (295°) on material collected by the ‘Goldseeker’ off the coasts of Scotland. We have now arrived at a more mature stage in our researches and the present work may be taken as superseding our previous taxonomic ideas. Tee METHODS Laboratory. The samples were collected either by means of the Holme Vacuum Grab or by the Van Veen Grab with a number taken by small Gravity Corer. The first 247 stations were fixed by sextant readings of landmarks, the rest by Decca Navigation System. All samples have been stored in glass jars in formalin buffered with borax and the foraminifera picked from 10 ml cuts washed over a 200 mesh screen (Brit. Stand. Aperture 75 microns). Rose Bengal was used as a stain for protoplasm. Flotation in heavy liquids was found an inadequate means of separating the foraminifera from the sediment and particularly inefficient in the coarser fractions. Allsamples have therefore been picked by hand to allow proper statistical analysis of the results. Foraminifera have also been collected from seaweeds and picked from sediments scraped from cobbles and boulders with a blunt knife. Most of the species have been illustrated by scanning electron micrographs. In this case the specimens have been cemented to aluminium stubs by ‘dag’ (a suspen- sion of silver in alcohol) and coated by aluminium in vacuum before scanning and photography. This technique emphasizes surface detail but does not reveal internal characters, indeed it may obscure them, especially where the specimen is lamellar and the septa flush with the external wall. Where necessary, therefore, figures have been drawn by light microscope and camera lucida. These were drawn by Dr J. R. Haynes and carefully inked in by Dr K. Atkinson. A number of thin sections have also been made by a procedure close to that used for preparing thin sections of incoherent sediments used by Moore & Garraway (1963). Photographs of these sections were done by Zeiss Photomicroscope. Descriptwe. The synonymies have been restricted to important name changes and to citations from the North Atlantic and North Sea area with both figures and descriptions. In some cases citations with good figures only have been included. Other records are grouped in the distribution sections. ' Additional reference in addendum. CARDIGAN BAY RECENT FORAMINIFERA II A general diagnosis is given for each species as well as a description of a particular specimen. -In the descriptions care is taken to distinguish between the chambers visible on the periphery of trochospiral or planispiral forms and the number actually present in the successive whorls counted from the proloculus (as by Haynes, 1956). In biserial and triserial forms the angle of taper from the initial end to the widest part of the adult is given (as by Chamney, 1969). fil. . LOCATION; OF MATERIAL The specimens described are deposited in the collections of the British Museum (Nat. Hist.) and the registered numbers are given in the descriptions. In the case of the specimens illustrated by scanning electron micrographs the stubs have been presented (as removal from the well set ‘dag’ would undoubtedly cause damage or loss). All the sections illustrated may be found in the collection as well as all the other material, in conventional ‘one-hole’ slides. IV. ACKNOWLEDGEMENTS We are grateful to Professor Alan Wood for his vision in embarking on the Cardigan Bay Project and for his continued encouragement of our researches. We also owe a debt of gratitude to the U.C.W. and N.E.R.C. for the financial assistance that made this work possible. Thanks also go to the late William (Bill) Lucas, skipper of the ‘Antur’, and to Dr H. Jones and Dr J. R. Moore for their help at sea with the collection of samples, particularly during the extraordinarily severe winter of 1962/63. Numerous colleagues in this country and abroad have kindly sent copies of their work and specimens for comparison and special thanks are due to Dr’s C. G. Adams and R. H. Hedley for their encouragement and permission to examine collections in the British Museum (Nat. Hist.). We are indebted to Professor P. C. Sylvester-Bradley for permission to use the scanning electron microscope at the University of Leicester and to Mr G. L. C. McTurk for his skill in taking the photographs. Finally, we must express our heartfelt thanks for the efforts made on our behalf by members of the technical staff of the U.C.W., to Mr H. Williams for long hours spent in the darkroom and his expertise in making enlargements from the S.E.M. negatives; to Mr S. H. Garraway for making the thin sections; to Mr H. Edwards, _ Mr D. Jones and Mrs S. Davies for help with the picking, preparing an index of North Atlantic foraminifera and for checking the bibliography. Mrs C. Thomas drafted the location map and inked the figure of T. haynest. Miss M. Hughes, Miss G. Jones and Mrs P. Jones cheerfully coped with the problem of typing the manuscript. V- ,CLASSTRICATION Among the criteria available for the classification of the foraminifera are: wall structure, chamber arrangement, aperture form and the evidence of ontogeny J. R. HAYNES and the stratigraphical succession. There has been a continuing debate regarding the relative value of these features but lately the tides of opinion have set strongly in favour of the primary importance of wall structure, despite warnings that the evidence was inconclusive (Wood & Haynes, 1957; Reiss, 1963). Thus Loeblich & Tappan (1964b) state, ‘in the classification used by the writers, test mineralogy and wall microstructure are regarded as of primary importance’, and in their scheme the suborders and superfamilies are largely recognized on this basis. We believe this goes too far, leading to artificial groupings. Workers have been tempted to treat wall structure as a ‘key’ to classification, supposing it a non-adaptive character. However, Haynes (1965), has put forward reasons for the possible adaptive signifi- cance of changes in wall structure. It must also be remembered that all morpho- logical changes arise initially at the specific or subspecific level and wall structure cannot be exempt from this rule. Loeblich and Tappans’ scheme requires the independent origin of all the different wall structure groups from tectinous ancestors. For this reason optically granular forms are separated from what are considered to be their radial hyaline isomorphs and grouped in three new superfamilies. Thus granular Czbicides is separated from. radial Cibicides and placed in the new superfamily Anomalinacea, despite the fact that what was actually demonstrated by Wood & Haynes (1957) was that forms otherwise identical with Cibicidoides s.s. such as C. pseudoungerianus were found to be radial, and plano-convex forms otherwise identical with Czbicides s.s. were found to be optically granular. Towe & Cifelli (1967) have now shown that the difference between optically granular and radial wall structure is slight. It is the result of calcification on the tectin membrane, preferentially on the basal pinacoid, ooo! face, in the case of radial forms, and preferentially on the rhomb face, rorT, in the case of granular forms. They believe that these modes of calcification are so similar that it wouid be relatively easy to derive one from the other. Striking confirmation of this probability appears to be provided by the Nomion—Elphidium group. The optically radial, intermediate form Protelbhidium was described by Haynes (1956). Granular forms of Elphidium s.l., E. incertum Williamson, were described by Buzas (1966) and in this work we describe beautifully optically granular forms of Elpiidium s.s., E. exoticumn. sp. Matoba (1970) has suggested that a new genus should possibly be set up to include granular E. subincertum Asano but it is now clear that wall structure changes occur at the specific level in this group. It is thus obvious that the attempt to recognize the superfamilies Anomalinacea and Nonionacea on the basis of wall structure has to be abandoned. It is also apparent that the ‘septal flap’ is a gradually acquired, progressive feature in this group, of independent origin from that in the Rotaliidae. For this reason we have decided to tread a conservative path in regard to classification with no attempt to recognize categories above the family level. The family Discorbidae is also interpreted in the wide sense to include for the time being Rosalina s.l. and ‘Glabratella’. There are a number of reasons for taking this course. Loeblich & Tappan (1964a) have figured topotypes of Discorbis vesicularis Lamarck, the genoholotype, which show it to be a biconvex form with markedly overlapping umbilical lobes on the ventral side hidden beneath a vesicular mass of CARDIGAN BAY RECENT FORAMINIFERA 13 secondary calcite. According to these authors thin sections show the wall structure to be radial and monolamellid, contrary to Reiss (1963) who considered this species bilamellid with tooth plates. Loeblich & Tappan (1964b) follow Reiss in placing Rosalina in a separate family (Rosalinidae) and accept his statement that R. globularis, the genoholotype, is bilamellid. However, although Reiss says that R. globularis is unambiguously designated and well known it is clear frem his dis- cussion of Discopulvinulina Hofker that his specimens are almost certainly not the same as the specimen selected by Loeblich & Tappan as neotype (1964a). He refers to Cushman’s view that R. bradyi is merely a variety of R. globularis which indicates he is following Cushman’s conception of the species. As we show below, North Atlantic references to R. globularis, including Cushman (1931) and Hofker (1951a), refer to R. anomala Terquem. This species appears to be monolamellid but it is difficult to be certain and it has coarse pores on the dorsal side. Specimens we place under R. ivregularis do appear to be bilamellid but optically granular. At the moment, therefore, the evidence for removing Rosalina to another family and superfamily (Orbitoidacea) seems weak, particularly in view of the difficulty of interpreting the wall structure. It is also quite possible that the bilamellid condition first arose as a progressive feature in this group. Loeblich & Tappan (1964a) have transferred discorbids with umbilical aperture, radial ornament and plastogamic reproduction, to Glabratella and the family Glabratellidae. They have transferred the Glabratellidae to the Orbitoidacea because Reiss has found a bilamellid wall in Conorbella (considered synonymous with Glabratella). But the type of Glabratella, G. crassa Doreen is Eocene and the wall structure and mode of reproduction are unknown. Dziscorbis baccata (Heron- Allen & Earland) = D. wrightit (Brady) is plastogamic and may be bilamellar (Pl. 30, fig. 4) but appears closer to Discorbis s.s. than Doreen’s species. Until we know more about reproduction in the whole group it is merely confusing to transfer species with radial ornament to Glabratella. Yor instance Le Calvez & Boillot (1967) transfer Rosalina milletta (Wright) to Glabratella which in Loeblich and Tappans’ scheme would put it in another super family, thus separating it completely from the closely related R. nitida = R. williamsom (Chapman & Parr). The genus Gavelinopsis, genoholotype G. praegert (Heron-Allen & Earland) is distinguished from Rosalina largely on the basis of its prominent umbilical plug. However, as we show below, this is not always present and cannot be considered a basis for sound generic subdivision, particularly as Loeblich & Tappan (1964a) figure species of Discorbis with plugs. For the present, Asterigerinata, genoholotype A. dominicana Bermudez, is left in the family Asterigerinidae, although Reiss (1963) claims the chamberlets are secondary, not primary as in Asterigerina and transfers it to the Conorboidinae (Conorbidae). However, Loeblich & Tappan (1964b) transfer Conorboides to the aragonitic, Ceratobulimininae, so further work is required. But we do follow Reiss (1963) in placing Buccella in the Rotaliidae and agree that it is close to Ammonia but with dense granules obscuring the sutural fissures and giving the appearance of secondary apertures. It will be seen that our ideas on supra-generic classification in general and 14 J. RK. HAY NES especially on the value of wall structure show something of a return to those of the ‘English School’. Williamson (1858) first recognized the three major wall structure eroups, in particular the opaque calcareous (porcelainous) wall of the Miliolids, but his caution is well expressed by his statement that these differences “were at least of specific value’. This caution was well justified in view of the outer, aggluti- nated wall in many species of Quinqueloculina, such as Q. aspera, which could be taken to show the trend to Miliammina. ‘This genus, with grains bound in the tectin lining, probably first arose as an adaptation to the extensive brackish water areas so typical of Interior North America in the late Jurassic and Cretaceous. It is plain that a rigid application of wall structure leads to a horizontal classification. This may provide convenient pigeon holes but it hinders the study of lines of descent. Vio SYSTEMATICUDESCRIP LIONS Family ASTRORHIZIDAE Brady, 1881 Genus HALYPHYSEMA Bowerbank, 1862 Halyphysema tumanowiczti Bowerbank (Pl he 6 Pi a ne. 12) Halyphysema tumanowiczii Bowerbank, 1862 : 1105, pl. 73, fig. 3; Norman, 1878 : 274; Kent, 1878 ::'68, pls 4;.5; Lankester, 1879 :.475, pl. 22, figs 1-11: Brady, 1884 : 281,) pl y27. figs 4,5; Cushman, 1918 : 87, pl. 33, figs.1,. 2; Loeblich’& Tappan, 1958: 124, pl. 1, igs 12 (figs of lectotype); 1964a : C192, figs 108-6, 7. Squamulina scopula Carter, 1870 : 310, pl. 4, figs 1-11. DiaGnosis. Aspecies of Halyphysema in which the test consists of a single column, rising from a disc-like pedestal and gradually expanding to a brush-like head beset with sponge spicules. DESCRIPTION: (PI. 1,; fig. 6: PL. 3, fig..13.) Test. umlocular, fixed) by round, concavo-convex, disc-like pedestal which has bars within, elongate and gradually enlarging to the head which is flattened and has a slight neck, round in section, about five times as long as wide; aperture terminal, apparently single; wall thin, ‘collagenous’ with closely agglutinated quartz silt and interwoven sponge spicules; spicules subparallel to the wall in the lower part but sticking out at an angle from the head and neck. DIMENSIONS. Length 1:20 mm, maximum width 0-26 mm, MATERIAL. Four specirnens. VARIATION. The clavate body chamber may be straight or twisted and the sponge spicules on the head directed forwards or out at various angles as in the specimen described. Rarely, sponge spicules entirely predominate (Lankester, 1879). DEPosITORY. B.M.(N.H.) Slide 1970 : 11 : 26: 1-3. Stub 1970 : 11 : 26 : 625. PROVENANCE. Specimen described, CB 647. CARDIGAN BAY RECENT FORAMINIFERA T5 REMARKS. This remarkable foraminifer, ‘bristling with borrowed spicules’, as Brady remarked, was originally regarded as a sponge before its true affinities were recognized by Carter. Carter’s description includes these interesting details about the soft parts, ‘Animal occupying the cavity of the test, consisting of semitransparent yellowish sarcode charged with granules and oil globules, frustules of Diatomaceae, especially Melosiva, dark brown bits of Fucus, and reproductive cells’. Details of the wall are shown in Pl. 1, fig. 6. It will be noted that in some cases it is the pointed tip in other cases the rounded base of the sponge spicule that sticks out. Hedley & Wakefield (1967) have shown that the inner lining of the test is of fibrous protein, possibly collagen, imparting a flexibility that may be of adaptive value in the turbulent zone. DISTRIBUTION. This species occurs as a fixed form among weeds in the Laminarian zone. It is possibly widespread around Great Britain and it appeared as a juvenile form on weed covered cobbles gathered from Sarn Cynfelyn and kept in a tank for some months. The original specimens were from Hastings (Sussex) and Carter’s specimens came from Budleigh Salterton, Devon, found on Laminarian holdfasts and the fronds of Phyllophora. Other British records are Wembury, Devon (Hedley & Wakefield, 1967); Torbay, Devon (Parfitt, 1878); Jersey (Kent, 1878); Dublin Bay (Haddon, 1886); Colwyn Bay and Dee (Siddall, 1878, 1886); Clare Island (Heron-Allen & Earland, 1913b). Genus HIPPOCREPINA Parker, 1870 Hippocrepina species A (Pl. 2, fig. 4; Text-fig. 2, nos 1-4) Diacnosis. A species of Hippocrepina with subovate to elongate ovate test, slightly irregular but tending to be widest at the apertural end which is slightly produced and truncate with the aperture within a depression. ns 0:0 1.0mm. Fic. 2, 1-4. Hippocrepina species A. 1-3, views of broken specimen containing dried protoplasm; 4, oval specimen. J. R. HAYNES DESCRIPTION. (PI. 2, fig. 4.) Test subovate with truncate ends, round in section and widest above the mid point; apertural end produced into a rounded collar surrounding the small, circular, terminal aperture; wall strongly built, mainly of quartz silt with some mica and dark minerals, smooth exterior coat now partially - removed, faint parallel constrictions visible towards the base, grey in colour. Dimensions. Length 0-8 mm, diameter 0-46 mm. MATERIAL. About 10 specimens, some collapsed and distorted. VARIATION. As shown by the text-figure there is a range of shapes from subovate to subcylindrical and the faint grooves are more conspicuous in some specimens. No. 4 shows a collapsed form in which the aperture cannot be made out. These specimens were alive on collection and the broken one illustrated is filled up with a silty mass of protoplasm and dark waste products apparently including diatoms. The wall in this specimen is about 40 microns in thickness. 7 DEPository. .B:M:(N.H.) Slide 1970 : 11 : 20: 4-5. . Stub. 1070. : 1m 26 3526. PROVENANCE. Described specimens, CB 413. REMARKS. ‘This species differs both in shape as well as in apertural characters from Hippocrepina pusilla Heron-Allen & Earland and Hippocrepina oblonga Pearcey. There is some resemblance between our specimens and Hippocrepinella acuta Hoglund but his specimens are all much smaller, with stronger constrictions and pointed initial ends. The wall is also much thicker and the aperture is not countersunk. Incidentally, Hoglund’s specimens should properly be included in Hippocrepina as Hippocrepinella was diagnosed by Heron-Allen and Earland as possessing double apertures and thin wall. DISTRIBUTION. All the specimens so far recovered are from Tremadoc Bay in northern Cardigan Bay. Genus MARSIPELLA Norman, 1878 Marsipella elongata Norman (Weds 3) fig. 14) Marsipella elongata Norman, 1878 : 281, pl. 16, fig. 7; Carpenter, 1881 : 561, figs d, e, f; Brady, 1884 : 264, pl. 24, figs 10-19; Flint, 1899 : 270, pl. 12, fig. 1; Cushman, 1918 : 23, pl. 8, igs 2, 3; Avnimelech, 1952 : 66, fig. 15. } DIAGNOSIS. An irregularly curved species of Marsipella tapering towards the extremities which become tubular and are composed of sponge spicules in contrast to the coarse sand grains of the body chamber. DESCRIPTION. Test broken with tubular extensions lost; unilocular, an irregular tube with roughly agglutinated wall of angular quartz grains up to about 0-3 mm CARDIGAN .BAY:- RECENT: FORAMINIFERA 17 in Maximum diameter; subround in section; original test presumably open at both ends. DIMENSIONS. Length 3-3 mm. MATERIAL. Six broken specimens. Deposirory. B.M.(N.H.) Slide 1970 : 11 : 26: 6-8. Stub 1970: II : 26 : 650— O51. PROVENANCE. Specimen described, CB 318. ReMARKS. According to the original description the wall is of coarse sand grains ‘interspersed here and there with a sponge spicule’ but the mouth opening is formed by a ‘faggot’ (bundle) of sponge spicules. However, Brady (1884) found exceptional individuals made up of quartz grains throughout and similar individuals occur in Carpenter’s Lightning material in the British Museum which also includes wholly spicular forms and specimens built of the tests of other foraminifera. It is therefore a mute point as to whether our specimens are all broken as they do not show the faggots of spicules and so they are questionably referred to the species. A number of specimens were also recovered in which the wall is composed of a sheaf of shell fragments (Pl. 3, fig. 15, CB 360) and a single specimen apparently composed of overlapping mica flakes (Pl. 3, fig. 16, CB 15). These are questionably referred to Marsipella species A and B, but could be worm tubes. DISTRIBUTION. This species was described from Porcupine station No. 87, lat. 59°35’N, 9°W and appears to be widespread in the N. Atlantic: Warm Faroe Channel (Brady, 1884; Pearcey, 1890); West of Ireland (Brady, 1884; Wright, 1889); Canaries and Azores (Brady, 1884); Western Atlantic (Cushman, 1918); Caribbean (Flint, 1899). Other records are: Indian Ocean, off Zanzibar (Stubbings, 1939); Antarctic (Chapman & Parr, 1937); South Atlantic, off Argentina (Boltovskoy, 1961). Genus TECHNITELLA Norman, 1878 Technitella teivyense Haynes n. sp. (Pl. 1, figs 1-4) DESCRIPTION. (Holotype Pl. 1, figs 1, 2 and 4.) Test attached, unilocular, roughly cylindrical and rising from an encrusting base, tapering slightly to the large, round aperture; wall an open network of sponge spicules directed forwards at about 45° to the axis of growth and piercing the tectin lining to intrude into the body chamber, markedly brushed forward around the aperture; aperture with in- ternal tectin collar. DImMENsSIons. Height approximately 0-70 mm. MATERIAL. Six specimens, or groups of specimens, attached to algae, 14 detached specimens. VARIATION. This species occurs as a cluster of individuals arising from the encrusting mat-like ‘base or as single individuals. The shape of the body chamber : | J. R. HAYNES is varies from narrow to stoutly cylindrical, some specimens tapering markedly towards the aperture. There is no evidence of branching of the cylindrical body chamber so the colonies appear to be composed of separate individuals. Specimens up to 2 mm length occur. } Depository. B.M.(N.H.) Stub 3970: 11 : 26: 741-743 (holotype and para- types). PROVENANCE. Holotype, CB 647. Paratypes, CB 647. REMARKS. In 1967, Haman put forward good grounds for the supposition that T. lezumen had hitherto been misinterpreted, the former attachment end being mistaken as the aperture and the test figured upside down. Additional collecting in south Cardigan Bay now makes evident that our material is specifically distinct from 7. legumen and T. melo. In particular the rough, open, spicular structure of the wall in our form is quite different from the delicate, close set, warp and weft structure of T. legumen and the densely moulded wall of T. melo, well described by Norman as resembling the matted, fibrous surface of a coconut. This means that an attached habit in 7. legumen, although likely, still has to be proved and that our species can be placed in the genus Techmitella only tentatively. This brings up the question of the possible relationship of our form with Halyphysema which also has projecting spicules. However, this genus is also characterized by its definite attachment disc and club shaped head. DERIVATION OF NAME. Refers to provenance in Cardigan Bay (Bae Aberteifi in Welsh because the River Teivy enters the bay at the port of Cardigan). Pronounced as in neck-tie. Family SACCAMMINIDAE Brady, 1884 Genus PSAMMOSPHAERA Schultze, 1875 Psammosphaera parva Flint (Rie? He 13) Psammosphaera parva Flint, 1899 : 268, pl. 9, fig. 1; Cushman, 1918 : 35, pl. 12, figs 4-6. Psammosphaera fusca Schultze var. parva (Flint) Heron-Allen & Earland, 1913a : 17, pl. 2, figs 7, 8. Psammosphaera fusca Brady, part, 1884 : pl. 18, figs 2-4 only (not Schultze). DIAGNOSIS. A subspherical, fine grained species of Psammosphaera generally built round one or two sponge spicules. DESCRIPTION. Test free, subspherical, irregular in outline, apparently transfixed with four sponge spicules; unilocular; wall of agglutinated grains of silt up to 60 microns maximum diameter: no aperture but some small, irregular openings between the grains present. DIMENSIONS. Maximum diameter 0-20 mm. MATERIAL. Three specimens. VARIATION. Up to five attached sponge spicules occur. CARDIGAN BAY RECENT .FORAMINIFERA 19 Drvosrmory .B.M.(N.H.) Slide 1970 :.11.3:26.: 10.) Stub:1970 >. T1-> 26.: 686. PROVENANCE. Specimen described, CB 311. REMARKS. This species is distinguished from P. fusca by its finer wall and by the presence of one or more sponge spicules. Heron-Allen & Earland (1913<) supposed it ‘constructs its abode round the spicule in order to obtain the increased support afforded by its projections in supporting itself upon the surface layers of the bottom ooze’. DISTRIBUTION. This species was first described from deep water, 1o1g fathoms off the coast of Brazil. Around the British Isles it has been found in abundance only in Goldseeker Haul 288, Warm Faroes Channel (Heron-Allen & Earland, [913a). Other records include: N. Atlantic (Cushman, 1918); S. Atlantic, Pernam buco (Brady, 1884); Falklands (Earland, 1934); Antarctic (Chapman & -Parr, 1937; Harland, 1936; McKnight, 1962; Wiesner, 1931); Indian Ocean, coast of Madagascar (Braga, 1961); Pacific (Cushman, IgIo, 1921). Thus most records are from high latitudes and deep water. Genus Lagenammina Rhumbler, I911 Lagenammina arenulata (Skinner) (Pl, 2; fie. 17; Pl. 8; fis: 12; Text-fig. 3, nos 1-3) Reophax difflugiformis part Brady, 1884 : 289, pl. 30, fig. 5 only; Flint, 1899 : 272, pl. 16, fig. 2. reophax difflugiformis Brady subspec. avenulata Skinner, I961 : 1239. Proteonina difflugiformis (Brady) Cushman, 1918 : 47, pl. 21, figs 1, 2; Hoglund, 1947 : 53, ple te, 18; Cushman, 1948; 11, pl. 1, fig.-5; Hofker, 1960 : 235, fig. 7. Proteonina atlantica Parker, 1952a : 393, pl. 1, fig. 2 (not Cushman). Reophax atlantica (Barker) 1960 : 62, pl. 30, fig. 5 (after Brady). DraGnosis. An irregularly flask-shaped species of Lagenammina with slightly oroduced neck and coarsely agglutinated wall. Description. (Pl. 2, fig. 17; Pl. 8, fig. 12.) Test damaged with two holes and uppearing more bottle-shaped than it is in reality, unilocular, with greatest width Fic. 3, 1-3. Lagenammina arenulata, shape variations. 20 J. R. HAYNES from mid point to the base, tapering to a slight, stout, neck at the apex, subround in section with flattened base; wall coarsely and roughly agglutinated with angular quartz silt grains and some mica flakes up to 75 microns In diameter in a finer matrix; aperture oval, with slight neck and well formed lip of smoothly cemented smaller erains up to 30 microns in diameter. | | DIMENSIONS. Maximum length 0-50 mm, width 0-20 mm. MATERIAL. Twenty-three specimens. VARIATION. Most of the specimens are somewhat smaller than the one described above, those illustrated in the text-figures averaging 0-30 mm in length. As shown by Text-fig. no. I an occasional large sand grain is attached to the wall. The test although slightly irregular is generally subround at the base and consistently tapers to a rather short, stout aperture from about mid point. Deposirory. 'B.M.(N.H.) Stub 1970 :-11 : 26 : 644. : Slide 19071 : 23 16: 1-4: PROVENANCE. Specimen described, CB 413. Other specimens figured, CB 646. REMARKS. Brady included a number of different forms under Reophax difflugi- formis in the Challenger Report. Our specimens are close to that shown in fig. 5 which has been distinguished as subspecies avenulata by Skinner. As this form differs in shape, wall structure and apertural details from the type of Reophax diffiugifornus 1879 we have raised the name to specificrank. In fact, apart from the lack of apertural neck, L. avenulata is closer to L. atlantica Cushman. This is undoubtedly what led Parker and Barker to place Brady’s specimen in Cushman’s species. A number of references to L. diffiugiformis in the N. Atlantic and Arctic belong here though probably not those with long, narrow necks as illustrated by Parker (1952a) and Goés (1894). The specimens illustrated by Flint have necks that are unusually long but stoutly built like that in the type. DISTRIBUTION. The type was discovered at Porcupine Station 47 in the Faroe Channel, N. Atlantic. Other good, figured references are: The Skagerak (Hoglund, 1947); N. Atlantic, common north of Lat. 35° (Cushman, 1918); Arctic, Nova Zembla and off Greenland (Cushman, 1944); New England (Parker, 1952a). Lagennamina cf. hancocki (Cushman & McCulloch) i (Pl. 2, figs 1 ra Bie, fie. to) See Proteonina compressa Cushman & McCulloch, 1939 : 42, pl. I, fig. 10 (renamed hancocki 1948). DESCRIPTION. Test unilocular, oval with greatest width about midpoint and tapering slightly to the truncated apex, compressed; wall coarsely agglutinated of angular quartz silt up to 60 microns in diameter in a matrix of finer grains, small angular openings between the grains resembling pores about 2 microns in diameter; CARDIGAN .BAY “RECENT: FORAMINIFERA aT. aperture large and round with smoothly cemented lip of small grains about 5-8 microns in diameter. Dimensions. Length 0:23 mm, maximum width 0-15 mm. MATERIAL. One specimen only. Derostory. - .5.M:AN/H:) Stub 1970: 1 : 26 : 573. PROVENANCE. CB 156, Dovey marshes. REMARKS. This species resembles L. hancocki in its coarse wall, compression und in the form of the aperture but 1s more elongate oval. Genus HEMISPHAERAMMINA Loeblich & Tappan, 1961 Hemisphaerammina bradyi Loeblich & Tappan (PL. 6, figs x, 2) WVebbina hemispherica Brady, 1884 : 350, pl. 41, fig. 11 (not Parker, Jones & Brady = Tvocham- mina (Webbina) ivvegularis (d’Orbigny) var. hemisphaerica, 1866). Temisphaevammina bradyi Loeblich & Tappan, 1957 : 224, pl. 72, figs 2a, b. Diacnosis. A smoothly finished species of Hemisphaerammina with almost serfectly hemispherical test. DEscrRIPTION. Test attached to a quartz grain, unilocular, almost perfectly remispherical in side view, subround in section; wall of fine, angular silt grains n a finer matrix with rare spicules, smoothly finished; no aperture visible although here is a slight circular depression to one side. Dimensions. Maximum diameter approximately o-2 mm, maximum height upproximately 0-1 mm. MATERIAL. One specimen only. DEPOSITORY.” ; B/M.(N.H.) Stub 1970:: 11.:'26°: 626. PROVENANCE. CB 61. ReMARKS. Although much smaller our specimen is otherwise identical with the specimens of Brady and Robertson, redescribed by Loeblich and Tappan, range 9:5 to 1°56 mm diameter. Doubt has recently been thrown on the protozoan, indeed, foraminiferal, affinity of this form as Adegoke et al. (1969) have noted Hemisphaerammina-like egg cases belonging to a recent gasteropod. Unfortunately our material is too limited to ulow us to help solve this question. | DistrisuTion. The holotype was dredged with other specimens from two localities, 5 and 7 miles respectively off the Durham coast (North Sea) at about 30 fathoms. J. R. HAYNES Family HORMOSINIDAE Haeckel, 1894 Genus REOPHAX Montfort, 1808 Reophax arctica Brady (Pl. 3, figs 8-12; Pl. 6, figs 4, 5, 7) Reophax arctica Brady, 1881 : 405, pl. 21, figs 2a, b; 1882 : 99, pl. 2, figs 2a, b; Parker, 1952a : 395, pl. 1, figs 6, 7; Loeblich & Tappan, 1953 : 21, pl. 1, figs 19, 20. Bigenerina artica (Brady) Cushman part, 1948 : 31, pl. 3, fig. 9 only. Dracnosis. A slender, slightly compressed species of Reophax with up to 12 chambers, slowly increasing in size and narrow, oval to crescentic aperture. DESCRIPTION. (Pl. 3, figs 10, 11; Pl. 6, figs 4, 5, 7.) Test slender, elongate, almost parallel sided in the Jast part, initial end pointed, apex slightly produced, slightly compressed, lobate; 10 chambers, the first four after the proloculus increasing rapidly in size as added, the last five very gradually with the final pair almost equal in size, last chamber oval with produced apex, early chambers wider than high, later ones becoming higher than wide; sutures between early chambers in- distinct, those between the final three chambers deeply impressed; wall of very fine, angular silt grains with larger grains up to 35 microns maximum diameter in a smoothly cemented finer matrix; scattered, angular pores present about I micron in diameter; aperture compressed oval (eye-shaped), terminal at the end of a slight neck with smoothly cemented lip. Dimensions. Length 0-39 mm, maximum width o-Io mm. _ Proloculus diameter approx. 20 microns. MATERIAL. Twenty specimens. VARIATION. As shown by the figures (PI. 3, figs 8, g) more irregular specimens occur than that described; occasionally with much larger grains in the wall. Derosirory. 3B.M.(N.H.)° Slide 1070:: 11 26; 11. Stub 1070 =19- 2ae567, 1970 : II : 26 : 705-706. PROVENANCE. Specimen described, CB 498. Others illustrated, CB 428 and CB 555. KEMARKS. Brady’s original description emphasized the slender and compressed shape of this species but the rather variable, oval to crescentic aperture revealed by our stereoscanner photos has, hitherto, not been noted. Other remarkable characters include the smoothly cemented matrix and apertural lip and the quad- rangular pores, well shown in PI. 6, figs 5 and 7. Our specimens are less compressed but otherwise the same as Brady’s specimens examined in the British Museum. Parker (1952a) has dealt with the erroneous ascription of the species to Bigenerina by Cushman in his paper on Arctic foraminifera (1948). : DISTRIBUTION. This species was described by Brady from the Novaya-Zemlya Sea. Later records confirm its common Arctic occurrence: off Greenland and in the Canadian Arctic (Cushman, 1948; Leslie, 1963; Loeblich & Tappan, 1953; A DEI EAN Shy ee tara tech eta aoe gee ie Pee seeesiaiiieee Siena ld ——— CARDIGAN BAYYRECENT FORAMINIFERA 22 Phieger; 1952). Other N-'Atlantic records. are: off Portsmouth, N. Hampshire (Parker, 1952a); Great Pond, Falmouth, Massachusetts (Said, 1953). South Atlantic records are: off Argentina (Boltovskoy, 1957, 1963). North Pacific records are: Bering Sea (Anderson, 1963; Cooper, 1964). These records indicate a cool or cold water distribution. Reophasx fusiformis (Williamson) (PI. 3, figs 3, 4) Proteonina fusifoymis Williamson, 1858:1, pl. 1, fig. 1; Hoglund, 1947: 52, pl. 4, fig. 21, text-figs 20, 21; Cushman, 1948 : 11, pl. 1, fig. 6; Feyling-Hanssen, 1964 : 219, pl. 1, fig. 12 (lian text). Reophax fusiformis (Williamson) Siddall, 1879 : 4; Brady, 1884 : 290, pl. 30, figs 7-10 (not 11); Roebhch & Tappan, 1955 :7, pl._1, figs 2.and 3a, b; Barker, 1960 : 62, pl. 30, figs 7-10, not 11 (after Brady). Diacnosis. An elongate, fusiform species of Reophax with strongly overlapping chambers, the septa (internally incomplete) marked externally by constrictions. DESCRIPTION. (Pl. 3, figs 3, 4.) Test elongate, fusiform with greatest width towards the middle, subround in section; apparently three chambers in all, tapering to the apex and strongly overlapping ; septa apparently incomplete marked externally by horizontal constrictions (undercutting); wall roughly agglutinated with large erains up to fine sand size in a matrix of fine silt; some angular pores about I micron in diameter; aperture terminal, large and round with lip of more regularly cemented, fine grains. DIMENSIONS. Length 0-55 mm, maximum width 0-17 mm. MATERIAL. More than 25 specimens. VARIATION. Some specimens are more irregular than that described with the occasional very large grain attached to one side. Drrosirory =. B:M.(N.H.).-Slide 1970-: 11.: 26-: 12-14. Stub ~1970. 7.11. : 26.: /97- | PROVENANCE. Specimen described, CB 4oI. REMARKS. This interesting species, genoholotype of Pvoteonina, was trans- ferred to Reophax by Siddall and Brady who noted the incomplete internal septa, marked externally by constrictions. These observations were confirmed by Loeblich and Tappan who chose a lectotype from Williamson’s material with three chambers and a paratype apparently having two. However, Barnard (1959) has complained that the selection of the lectotype does not agree with the original specimen described and certainly most of the specimens in the Brady collection at the British Museum appear only partially two-chambered. Feyling-Hanssen (1964) notes that Christian- sen found only some of many thousands of specimens examined to have internal septa. This indicates that there are grounds for retention of the genus Proteonina, j.-R. HAYNES possibly as a subgenus of Reophax, distinguished by incomplete development of the septa. It may be that strong overlapping of the chambers is linked with partial reworking of the previous chamber walls. 7 DISTRIBUTION. This species was first described from Skye, Scotland. Brady's specimens were also from off the west coast of Scotland at Loch Fyne and Cumbrae. It has been widely recorded around the British Isles but in the absence of figures these citations must be treated with reserve apart from Murray (1965a), specimens from Plymouth illustrated by a stereo pair. Brady also recorded it from the Porcupine Station, west of Ireland. | | Arctic records include: Cape Fraser (Brady, 1884); off Greenland (Cushman, 1948). ae records indicate a cool to cold water distribution. Reophax moniliforme Siddall (Pl. 3, fise17 5) Pl Gn fie.8) Reophax moniliforme Siddall, 1886 : 54, pl. 1, fig. 2; Heron-Allen & Earland, 1913b : 43, pl. 2, fig. 12. Reophax sp. Balkwill & Wright, 1885 : 328, pl. 13, figs 9, 22-24. Diacnosis. A subcylindrical species of Reophax with up to 12 chambers of about the same size. DEscRIPTION. (Pl. 3, fig. 17; Pl. 6, fig. 8.) Test elongate, slender and sub- cylindrical, round in section, initial part bulbous; 11 chambers, including the proloculus which is larger than the chamber succeeding it, gradually increasing in size, wider than high with truncate apex (barrel-shaped); sutures not much im- pressed, horizontal; wall of angular silt grains up to 18 microns diameter in a finer matrix, smooth finish, fragile and weakly cemented, ferruginous, scattered, angular pores up to about half a micron diameter; aperture terminal, large and round with rim of regularly arranged grains. ieee DIMENSIONS. Length 0-64 mm, maximum width 0-11 mm. Proloculus diameter approx. 80 microns. | MATERIAL. More than 25 specimens, mostly broken. , VARIATION. Many specimens show chambers of almost equal size (like the type figure) or even narrowing in width rather than gradually enlarging as in the specimen described. Many also show a pronounced waist after the proloculus. Chamber number and size appear to be closely related to proloculus diameter but the broken nature of most of the material precludes accurate measurement. els DEposiToryY. B.M.(N.H.) Slide 1970: 11 : 26:15. Stub 1970 : 11 : 26 : 708. :. Sia Specimen described. Station III, Clettwr Transect, Dovey - Marshes. 3 CARDIGAN BAY RECENT, FORAMINIFERA 25 REMARKS. This species is remarkable for its regularly built test but, un- fortunately, due to its fragility, it is usually found broken. This had previously led us (like Brady before us) to include it under Protoschista findens (Adams & Haynes, 1965). As noted by Heron-Allen and Earland the septation is ‘often very obscure’ and Siddall’s figure, ‘gives a very misleading impression on this point’. Both Heron- Allen and Earland as well as Balkwill and Wright describe specimens in which the wall is composed of evenly laid sponge spicules. We have found the species occurring most abundantly on the intertidal marshes of the Dovey, with considerable numbers living. DISTRIBUTION. This species was originally described from off the Little Orme’s Head, near Llandudno, N. Wales. Other British records are: Irish Sea, off Dublin (Balkwill & Wright, 1885); Clare Island, west of Ireland (Heron-Allen & Earland, 1913b) ; Christchurch, Hampshire (Murray, 1968) ; Jersey (Halkyard, 1889) ; Western Approaches (Murray, 1970). Family LITUOLIDAE de Blainville, 1825 Genus AMMOBACUEITES Cushman, Ig1Io Ammobaculites balkwilli Haynes n. sp. (Pl. 2, figs 2, 3; Pl. 29, figs 5, 6; Text-fig. 4, nos 1-5) Haplophragmium agglutinans Balkwill & Wright, 1885 : 330, pl. 13, figs 18-20 (not Spivolina agglutinans d’Orbigny). Diacnosis. A species of Ammobaculites with the uniserial part of 2-5 chambers tending to be built up on top of the initial coil, sub-cylindrical and generally erect Fic. 4, 1-5. Ammobaculites balkwilli. 1, holotype; 2-4, paratypes, all in side view. fe J. R. HAYNES with straight peripheral edge. Aperture large and round with lip formed by a ring of angular grains set on end. 3 Description. (Holotype, Text-fig. no. 1.) Test with last chamber broken open, crozier shaped with the planispiral portion subordinate to the uniserial part and only slightly wider, slightly compressed initially becoming round in section in the linear part and subcylindrical; about five planispiral chambers visible, eradually increasing in size, three uniserial chambers increasing in size only slightly, truncate and subovate in shape; sutures slightly impressed and distinct in the uniserial part, indistinct in the coiled part; aperture terminal, large and round with a protruding ring of elongate grains forming a lip; wall coarsely agglutinated, mainly of angular quartz grains in a white matrix of fine silt, with scattered grains of jasper, biotite and chert, apparently imperforate. | Dimensions. Length 0-67 mm, maximum breadth of uniserial part 0-17 mm, breadth of planispiral part 0-18 mm. MATERIAL. More than 20 specimens. Abundant in the Dovey Marshes. VARIATION. There is considerable variation in chamber shape and growth rate in the uniserial part. In some cases the last chamber is smaller, Text-fig. 4 and in others the chambers become inflated and wider than high, Text-fig. 5. However, despite this there is a general tendency for the uniserial part to be straight and cylindrical and built on top of the initial coil (an extreme example being shown in Text-fig. 4 (where there is a switch in growth direction of about go°). The figures show the variation in grain size with particles of over 0:Io mm being incorporated, including in one case a foraminifer test, diameter 0-15 mm, Pl. 2, fig. 3. The larger grains and the coloured minerals (shown in black) are scattered in a groundmass of rather more constant size, about 15 microns in diameter, in turn embedded in a matrix of the finest silt. This species appears to select darker grains, including tiny fragments of coal, a fact which recalls the former sea borne coal shipments into Aberdovey. There is very little calcareous cement in specimens from the upper estuary and these may be quite fragile. DEPosiTorY. . B.M.(N-H.) Slides 1970°: 11 ; 20:: 26 (holotype), 1970-2] Zo: 17-21. (paratypes). ~Stub 1970 : 11 : 26: 518; 1970: It : 26: 744 (watatypes). Section 1970 : II : 26 : 468 (paratype). PROVENANCE. Holotype and figured specimens, Station III, Clettwr Transect, Dovey Marshes. _ REMARKS. Specimens identical with ours were collected by Balkwill and Wright irom the Irish Sea near Dublin and ascribed to Haplophragmium agglutinans (d’Orbigny) = Ammobaculites agglutinans. One of their drawings showing a specimen with three uniserial chambers is very similar to ours shown in Pl. 3, fig. 2. the other shows a large, erect specimen with five chambers in the uniserial part. [he drawings are very good and show the grain size and scattered dark minerals very well. _D’Orbigny’s species which is from the Miocene differs in its much larger total — size, larger initial coil and more numerous chambers. CARDIGAN BAY. RECENT FORAMINIFERA ag The closest relative among species previously described appears to be A. josephi of Acosta (1940) from 7 fathoms near Dogs Reef, Cuba. This form is similar to ours in overall size as well as grain size, with small initial coil and four chambers in the uniserial part. However, it differs in growth rate with the final chamber making up more than one-third of the test and in its small aperture without a lip. It also differs in being more irregular and, apparently, in being slightly compressed (although described as ‘strongly cemented’). N.B. Dr Ronald Walker of the History Dept., U.C.W. was kind enough to translate Acosta’s description from the original Spanish. DISTRIBUTION. This species occurs on both sides of the Irish Sea. It occurs abundantly on the marshes of the Dovey Estuary and its comparative rarity in the open sea may be explained by the rapid break up of the test after death under ordinary marine conditions. DERIVATION OF NAME. | In honour of F. P. Balkwill, co-discoverer of this species in 1885 and co-author of the first and only comprehensive and illustrated account of Irish Sea foraminifera. Genus HAPLOPHRAGMOIDES Cushman, Igto Haplophragmoides wilberti Anderson (Pl. 2, fig. 1; Pl.-20, fig..7; Fext-fig. 5, nos 3-7) Haplophragmoides wilberti Anderson, 1953 : 21, pl. 4, figs 7a, b; Todd & Bronniman, 1957 : 23, pl-evhesi 28; 29; odd &-Low, 1961 : 13, pl. 1, fig...5. ? Cribrostomoides jeffreyst Lutze, 1965 : 89, pl. 15, figs 10-13 (not Williamson). Diacnosis. An involute, slightly inflated, smooth species of Haplophragmoides with eight or nine chambers gradually increasing in size as added. Small umbilicus on each side filled with the lobed ends of the chambers. DESCRIPTION. (Text-fig. nos 3, 4.) Test with last chamber broken, semi- inflated with slightly flattened sides and slightly irregular outline in equatorial view, lobate with rounded periphery; planispiral and involute with small umbilicus on each side; eight chambers visible only, slowly increasing in size as added, the rounded, lobate ends filling the depressed umbilical area; sutures distinct, slightly depressed, straight to sigmoid at an angle of approximately 40° to each other; aperture not present but foramen of penultimate chamber visible as a low, peripheral slit at the basal suture beneath a lip; wall tectinous with very fine silt grains, amber to brownish-white in colour with smooth, glossy finish; slight depressions show a tendency towards collapse. DIMENSIONS. Maximum diameter 0-39 mm, maximum width 0-15 mm. MATERIAL. More than 25 specimens, some collapsed and some distorted. VARIATION, Specimens with seven to nine chambers visible externally occur with a maximum diameter of 0-53 mm. As shown by the text-figures there is considerable variation of outline and distorted specimens occur which appear more ro 28 J: Ro HAYNES inflated and umbilicate because more depressed. A larger specimen, referred to Haplophragmordes species A, is shown in Text-figs 1, 2. This specimen has fewer chambers visible, six and one half only, lacks umbilical lobes and is more globose with faster rate of chamber size increase, showing some resemblance to H. colum- hiensis Cush. and the smaller H. bonpland: Todd & Bronniman, but more finely arenaceous. Depository. B.M.(N.H.) Slide 1970 : 11 : 26 : 22-25. Section roe SqEIec 20. 466. Stub 1970: 11 : 26:570. Haplophrag edie. species A, 1971 : 2: 16.: 8. PROVENANCE. Figured specimens from the High Marsh Juncetum of the Dovey Estuary, Clettwr IA. Haplophragmoides species A (Text-fig. no. 1) CB 641, marshes at Porthmeirion. REMARKS. Our specimens with their tectinous walls, tendency to cig chambers visible and slight apertural lip seem to fall well within the range of variation given for the species by Anderson, though less well grown and with less marked umbilicus than topotypes in the British Museum collections—Slide 1957 : 7:7: 9 : 75-76. As he noted, this species differs from H. subinvolutum, from the Pacific coast of the ; U.S.A., in lacking the pronounced apertural hood. Also it differs in showing eight , ae Peele Calne y a See oo | 6 7 0.0 0.5 mm. Pic. 5. 1,2. Haplophragmoides species A, side view and apertural view. 3, 4. Haplo- phragmoides wilberti, described specimen, side view and apertural view. 5-7. Haplo- phragmoides wilberti, Shape variations. 8, 9. Cribrostomoides jeffreysii, described specimen, side view and apertural view. 10. Cvibrostomoides jeffreysii, larger specimen with overhanging apertural face. CARDIGAN BAY RECENT »FORAMINIFERA 29 or nine rather than six or seven chambers externally and in being more closely involute. As illustrated by the stereoscanner photo (PI. 2, fig. 1) the wall structure is seen to be very fine and the surface glossy, the sutures hardly visible by this technique. DISTRIBUTION. This species was first described from brackish water and inter- tidal environments in Louisiana. The only other records are the Gulf of Paria (Todd & Bronniman, 1957); Rappahannock River, Virginia (Ellison & Nichols, 1970) and Martha’s Vineyard, Massachusetts (Todd & Low, 1961). It is interesting that these authors report joint occurrence with Jadammina macrescens which is the situation we find in the Dovey Estuary. If the specimens of Lutze belong here then the range of this form extends into the Baltic area also. Genus CRIBROSTOMOIDES Cushman, 1910 Cribrostomotides jeffreysii (Williamson) (ele 2, digs 5,0; Pl 8, fie: -9% Pl.29, fig..10; Text-fig. 5, nos 8-10) Nonionina jeffreysu Williamson, 1858 : 34, pl. 3, figs 72, 73. Haplophragmium jeffreysi (Williamson) Berthelin, 1878 : 24, no. 20. Labrospiva jeffreyst (Williamson) Hoglund, 1947 : 146, pl. 11, fig. 3, text-figs 128, 129; Parker, 1952a : 401, pl. 2, figs 15, 17-20. Alveophvagmium jeffreyst (Williamson) Loeblich & Tappan, 1953 : 31, pl. 3, figs 4-7. Laplophragmium canariense Brady (part), 1884 : 310, pl. 35, figs 1-3, 5 (not 4) (not d’Orbigny). Laplophrvagmoides canariense Cushman, 1920 : 38, pl. 8, fig. 1; Cushman, 1948 : 26, pl. 2, fig. 15. Laplophragmoides columbiensis Cushman, 1944: 12, pl. 2, fig. 1; Parker, 1948 : 238, pl. 4, fig..17 (not Cushman, 1925). DiAGNosiIs. A compressed species of Cribrostomoides with arcuate and protruding vpertural slit. The wall includes angular, glassy grains in a finer matrix and well srown specimens show slight uncoiling and large pseudumbilicus. DESCRIPTION. (Text-fig. nos 8, 9.) Test compressed, lobate with sub-rounded yeriphery; planispiral and involute with small umbilicus on each side; six chambers visible, increasing gradually in size as added, the last two making up about half he test ; septal sutures distinct, impressed, flexuous; wall thin, tectinous with angular slassy, quartz grains set in a finer matrix, fragile, white in colour; aperture areal, 1 protruding arcuate slit, with a slight neck with upper and lower lips, parallel to he basal suture. DIMENSIONS. Maximum diameter 0-31 mm, maximum width 0-12 mm. MatTertaL. More than 25 specimens but most of them small, less than 0-35 mm liameter. VARIATION. Our material includes specimens up to about 0-40 mm in size, as shown in Text-fig. no. 10, but most are about 0-30 mm in diameter and consistently how six or seven chambers externally with little variation in shape. Authors’ igures show much larger specimens, the type is about 0-5 mm in diameter and Parker describes specimens up to 0-83 mm from off New Hampshire. These speci- nens show a tendency towards uncoiling and with a slower rate of chamber size J. R. HAYNES increase up to seven or eight chambers at the periphery, the pseudumbilicus revealing the penultimate whorl. The tendency for the aperture to be tucked under the overhanging apertural face also becomes more marked with growth and is reflected in the curve of the septal sutures. Hoglund has been able to distinguish both a microspheric generation (averaging 20 chambers) and a megalospheric generation (averaging about 15 chambers) both showing seven to eight chambers in the second whorl and up to 24 whorls in all. The colour is variable in our population. The specimen described is white. Others are golden-yellow or even reddish, the Sienna brown of Williamson. : DEpository. B.M.(N.H.) Slide 1970 : 11 : 26: 26-28. Section 1970 : 12 : 26: 467... Stubi970 211 +267: 509. | PROVENANCE. Specimen described, CB 555. Additional figured specimen, CB 299. REMARKS. Our specimens are smaller than the type but are identical in ‘the striking contour, arenaceous texture and rich colour’ also in the characteristic ‘inlaid’, quartz grains appearing as ‘dark translucent specks’ in a finer matrix. Although, as Hoglund noted, Williamson’s diagnosis, ‘constitutes a brilliant excep- tion from the incomplete descriptions of earlier authors’,and makes clear the siphun- cular nature of the aperture, this species has been confused with others, in particular with Haplophragmoides canariense (d’Orbigny). However, d’Orbigny’s type figure shows a peripheral-basal aperture and this is confirmed by the redescription of the species made by Loeblich & Tappan (1964a) based on a specimen from the Philip- pines. As d’Orbigny’s species is the genotype the generic status of Nonionina jeffreysit has also been in doubt with successive transfers to Labrospiva and Alveophragmium. As shown by Loeblich & Tappan (Ibzd.) the latter must be restricted to species with alveolar wall so our species must be referred to Cribrostomoides which includes Labrospira as a junior synonym. Like many specimens referred to H. canariense N.W. Atlantic specimens referred to H. columbiensis also belong to Williamson’s species, as indicated by Parker (19524). This possibly applies also to the abnormal specimens referred by Heron-Allen & Farland (1913b, 1916a) to H. canariense. DISTRIBUTION. Williamson recorded this species from a number of localities down the western seaboard of Great Britain from the Shetlands to Cornwall, as well as from Davis’ Straits in the Arctic. Listed records of H. canariense in the same area, such as Siddall (1879) and Worth (1900, 1902) probably refer to this species also. It is listed by Murray from Plymouth (1965a) and Christchurch (1968) and by Atkinson (1970) from the Scillies. ; Other records seem to confirm a general temperate to cold water range for this form with a number for the N.W. Atlantic and Arctic: New England (Cushman, 1944; Parker, 1952a); Canadian Arctic (Cushman, 1920, 1922; Loeblich & Tappan, 1953; Vilks, 1969); off Nova Scotia (Barbieri & Medioli, 1969) South Atlantic records are: Estuary, Rio de la Plata (Boltovskoy, 1957); _ continental platform between San Tome and Rio de la Plata (Boltovskoy, 1961). CARDIGAN BAY RECENT. FORAMINIFERA 31 Outside the Atlantic there are records from: Off the Pacific coast of Japan (Uchio, (962) and Prince Edward Island S. Pacific (Brady, 1884). Family TEXTULARIIDAE Ehrenberg, 1838 Genus SPIROPLECTAMMINA Cushman, 1927 Spiroplectammina earlandi (Parker) (Pl. -2, fig. 57,Pl: 8, fez 11} extularia elegans Lacroix, 1931 : 14, fig. 11; 1932 : 8, figs 4 and 6, not 5 (not Plecanium elegans Hantken). rextulavia tenuissima Farland, n. name, 1933: 95, pl. 3, figs 21-30; Hoglund, 1947 : 176, pls 13, fig. a, text-figs 154, 155, 161 (not Hausler). | Pextuluvia eavlandi Parker, n. name, Thalmann in Phleger, 1952b : 86, pl. 13, figs 22-23; Parker, 1952b : 458 (cf. tenuissima in text, new name in footnote); Feyling-Hanssen, 1964 : 238, pl. 3,.figs 9, 10. Pextularia aft. earlandi Phlieger, Feyling-Hanssen, 1964 : 236, pl. 3, fig. 8. pivoplectammina elegans (Lacroix) Norvang, 1966 : 14, pl. 1, fig. 24; pl. 2, fig. 11. Diacnosis. A long slender species of Spiroplectammina with up to 15 pairs of -hambers which only gradually increase in size as added. Angle of taper between co-and:20-. DESCRIPTION. «,.(Pi. 3, fig.5; Pl.8, fig. 11.) “Test broken in transfer to thé stub © it appears slightly less regular than in fact it was originally, elongate, slender, vith bluntly rounded initial part and apex, periphery rounded, lobate; initial plani- piral cou of four chambers followed by Io pairs of chambers gradually increasing n size as added, oval in shape; sutures distinct, impressed; wall ferruginous, of ngular silt grains, including shell material, apparently arranged in a single, flat ayer, of varying sizes up to 50 microns in diameter; small angular openings about - micron in diameter which may be pores; aperture an arched opening at the basal uture in the median line. DimENSIons. Length 0-56 mm, maximum width 0-14 mm. Angle of taper bout 18°. MATERIAL. Five specimens. VARIATION. One specimen shows quite markedly the tendency of the chambers o overhang the suture line; slightly shown by the specimen described. The material s insufficient for proper analysis of dimorphism but proloculus diameters appear o be near 20 microns, within the upper limit given by Lacroix. IDEROsITORY-..B:M.(N-H:)-.Slide1970°: 11 : 26°: 29~31: Stub 1970 1,11-: 26: 2%. PROVENANCE. Specimen described, CB 34. REMARKS. The tortuous synonymy shows the difficulties authors have had with laming this form. The chief problem that remains is the question of the exact dentity of the Mediterranean material of Lacroix and the South Georgia specimens fi Earland. Earland, after exchange of material with Lacroix, considered them 32 |). Re HAYNES one species but Feyling-Hanssen, after the matter had been raised again by Parker, considered them two different species, one inhabiting cold waters and one, T. aff. earlandi, being a temperate to warm water form. However, after examination of the South Georgia specimens in the British Museum we consider there are no grounds ~ for separating them on the basis of wall structure or colour from the boreal forms. Both grey and ferruginous specimens occur in our material; Earland’s specimens are brownish. Inany case, even if the material were divided, the name T. earlanat must be applied to the material of Lacroix and a new name found for Earland’s, South Georgia material. Norvang (1966) has attempted to preserve the name elegans of Lacroix after transferring the genus to Spiroplectammuina but this appears to be against the Rules, Article 57. Revival of secondary homonyms, Article 59c, is only allowed for names rejected after 1960 (Stoll et al., 1961). The name earland: is also to be preferred on grounds of stability as ‘Plecanium elegans’ could possibly be transferred from Textularia to Spiroplectammina also. A specimen from the Humber, referred by Mills (1900) to T. agglutinans d’Orb. may also belong here. DISTRIBUTION. This species was originally described from the Mediterranean. Subsequent records from the N. Atlantic area are: off S.W. Ireland and Faroes (Parr, 1950) ; Skagerak and Kattegat (Hoglund, 1947) ; Holocene of Norway (Feyling- Hanssen, 1964); Long Island Sound—Buzzards Bay area (Parker, 1952b); Canadian Arctic (Phleger, 1952b); Western Approaches (Murray, 1970). Records from the Gulf of Mexico include: N.E. Gulf (Parker, 1954); Mississippi (Lankford, 1959); off Texas and Mexico (Phleger, 1g6ob). South Atlantic records include: tide pools along the Patagonia coast (Boltovskoy, 1963); 25 stations around South Georgia (Earland, 1933). North Pacific records include: off Japan (Matoba, 1970; Uchio, 1959, 1962); California coast (Arnal, 1958; Bandy, 1963; Walton, 1955; Zalesney, 1959). Antarctic records include: ‘widely distributed’ (Parr, 1950). Spiroplectammina wrightii (Silvestri) (Pi. 3) ties an,.2) Spiroplecta sagittula Wright, 1891 : 471; I902a : 211, pl. 3, figs 5-8 (not Textularia sagittula Defrance). Spivoplecta wrightit Silvestri, 1903 : 59, text-figs 1-6; Heron-Allen & Farland, 1O16b : 42; pl. 6, figs 7-10; Cushman, 1922 : 5, pl. 4, figs 5-8. Spivoplectammina wrightii (Silvestri) Cushman, 1949 - 6, pl. 1, figs 2-4. Textularia sagittula Brady, 1884 : 361, pl. 42, figs 17, 18; Balkwill & Wright, 1885 : 332, pl. 13, figs 15-17; Lacroix, 1929 : 1, text-figs 1-12; Heron-Allen & Earland, 1930 : 72; Hoglund, — 1947 : 167, pl. 12, figs 3, 4; text-figs 143-146; Colom, 1952 : 18, pl. 5, figs 41, 42; Feyling- Hanssen, 1964 : 238, pl. 3, figs 4, 5; Norvang, 1966 : 11, pl. 1, figs 9-23; pl. 2, fig. 12 (not Defrance). Textularia cuneiformis Williamson, 1858 : 75, pl. 6, figs 158, 159 (not d’Orbigny). Textularia sagittula Defrance var. cunertformis Goés, 1894 : 36, pl. 7, figs 288-290 (not d’Orbigny). Textularia williamsoni Goés, 1894 : 36, pl. 7, 285-287 (nomen oblitum). Dracnosis. A compressed, carinate species of Spiroplectammina reaching about ae ay i S CARDIGAN BAY RECENT FORAMINIFERA 33 I mm in size with up to 14 pairs of chambers in the microspheric generation which is sagittate with angle of taper about 45° and with up to 12 pairs in the megalospheric generation which has a large initial coil and tends to become parallel sided. DESCRIPTION. (PI. 3, figs 1, 2.) Test compressed with rounded initial part and slight waist before the commencement of the parallel sided adult part, periphery lobate, carinate; initial part planispiral followed by seven pairs of chambers, the first three increasing fairly rapidly in size as added, the last four only gradually, twice as wide as high, sutures distinct, slightly impressed, almost horizontal; wall of angular silt grains set in a tectin lining, including shell material, up to 40 microns diameter, in a finer matrix, smoothly cemented; minute oval to quadrangular openings between the grains about I micron in size which may be pores; aperture a low slit at the basal margin of the last chamber in the median line. Dimensions. Length 0-65 mm, width 0-36 mm, thickness about 0-15 mm. Overall angle of taper about 35°. MATERIAL. More than 25 specimens but many damaged, particularly at the initial end in the microspheric generation and in specimens with smaller megalo- spheres. VARIATION. Specimens up to I mm length occur and apart from the tendency for specimens with large megalospheres to become parallel sided many show waisting at different points during growth with sudden expansion in breadth thereafter. This occurs in both generations. Because of the broken nature of the material it is impossible to emulate the exhaustive investigation of dimorphism carried out by Lacroix and Hoglund, but it can be said that the microspheric generation occurs rarely, microsphere about 20 microns diameter, the megalospheric generation much more abundantly, megalosphere between 50 and 80 microns diameter in Io speci- mens measured with up to 12 pairs of chambers. An initial planispire of four to five chambers occurs in both generations. IDePository..° B.M.(N.H.): Shde 1970.7 11 :.26.:32. Stub-1970 >: Ir : 26:: 722. PROVENANCE. Described specimen, Brit. Mus. Core 13. REMARKS. This species has been persistently confused with I. sagittula Defrance although the type figures of that species show a large inflated form, biserial through- out and about 3 mm long. The Defrance collection was apparently destroyed in the attack on Caen during the war (1944) according to Norvang (1966) but specimens which may reasonably be regarded as topotypes have been collected from the Pliocene of Sienna by Loeblich & Tappan (1964a). They are much larger and more inflated than S. wrightit and lack the planispiral initial part. A prime cause of the confusion that has long reigned was the fact that Defrance cited the Mediterranean as an additional locality for his species which led Lacroix to suppose that S. wrightit was synonymous with it. There is now no doubt that Lacroix actually was working with S. wright. This also means that the attempt by Norvang to set up a specimen of ‘T. sagittula = S. wrightii, from the Bay of Villefranche as neotype for Defrance’s species is unnecessary as well as offending against the Rules of Nomenclature. According to the Rules neotypes must be Cc 44 J) Reagan Ss based on material from the type area and as noted by Loeblich and Tappan, T. sagittula was originally described as a fossil from Italy which indicates the Pliocene, Sienna or Castel Arquato, localities of Defrance. A further consequence is that Norvang’s attempted redefinition of Textularia on the basis of its ‘calcitic’ wall is found to be based not on the genotype but on S. wright. This would suggest that a new generic name is required for ‘calcitic’ as against arenaceous species of Spiro- plectammina. However, we believe these differences to be of specific rather than generic significance, especially as S. earland1, accepted by Norvang in Sparoplectam- mina s.s. has according to our observations calcareous grains in its wall and his own thin section of 7. sagittula (pl. 2, fig. 12) = S. wrighti, includes ‘insignificant amounts of quartz grains’. Both may have pores. Textularia williamsont Goés is apparently a senior synonym of S. wright. According to Hoglund it probably represents the microspheric generation. How- ever, he found no trace of the specimens in Goés’ collection and the name must now lapse as a nomen oblitum, being out of use for over fifty years. Very detailed observations have been made upon this species by Lacroix, Heron- Allen and Earland and Hoglund. These indicate pronounced dimorphism with a strong tendency for two groups of megalospheric individuals, constituting the Ar and Az2 generations of Hofker. It is possible that Spivoplectammina sagittula of Hofker (1930) belongs here but _ there is doubt because he reports areal apertures and foramina in his population. DISTRIBUTION. British records include: off Rathlin Island, Northern Ireland (Wright, 1902a), South Irish Sea (Balkwill & Wright, 1885); Western Approaches (Le Calvez & Boillot, 1967; Murray, 1970); English Channel (Heron-Allen & Earland, 1g16b, 1930; Murray, 1965a); Western coasts of Britain (Williamson, 1858); Scillies (Atkinson, 1970). Other N.W. European records include: Bay of Biscay (Caralp, Lamy & Pujos, 1970); coast of Galicia (Colom, 1952); N.W. Atlantic (Brady, 1884); Belgian coast (Cushman, 1949) ; Skagerak (Hoglund, 1947); Holocene of Norway (Feyling-Hanssen, 1964). Mediterranean records include: Tyrrenian Sea (Silvestri, 1903) France (Lacroix, 1929, 1932; Norvang, 1966). A marked Lusitanian—Mediterranean concentration appears to be indicated. ; off southern Family TROCHAMMINIDAE Schwager, 1877 Genus TROCHAMMINA Parker & Jones, 1859 Trochammina astrifica (Rhumbler) (Pl. 4, figs 18-20) Troe hammina squamata astrifica Rhumbler, 1938 : 188, figs 29-31. lvochammuna astrifica (Rhumbler) Hoglund, 1947 2.206, pl. 15,-lg.,25 texte. 180) Diacnosis.. A concavo-convex species of Tvochammina with from five to seven chambers visible ventrally and regularly star shaped umbilical opening. i] t | | CARDIGAN BAY RECENT FORAMINIFERA 35 DeEscriPTIon. (Pl. 4, fig. 18, description of dorsal side from extra specimen, Pl. 4, figs 19, 20.) Test concavo-convex, compressed, periphery subangular, slightly lobate; chambers arranged in a low, trochoid spiral of about three whorls, all visible on the raised (rather flattened) dorsal side, gradually increasing in size as added and becoming long and low with slightly impressed, swept back sutures, only the last five visible on the concave, involute ventral side, sutures impressed, radial, excavated towards the open umbilicus making a regular, star-shaped figure with blunt points; wall of flat, angular silt grains up to 20 microns diameter (probably shell material) arranged in a neat mosaic parallel to the tectin base; aperture ap- parently a low slit at the basal suture of the last chamber on the ventral side and communicating with the open umbilicus beneath the chamber lobes. Dimensions. Diameter 0-26 mm, additional specimen 0-19 mm. MATERIAL. Two specimens only. Depository: B.M.(N.H.) Stub 1970 : Ir : 26 : 730-731. PROVENANCE. Specimens described, CB 519 and CB 594. REMARKS. Our specimens appear to be close to Rhumbler’s types though with five chambers visible on the ventral side rather than six or seven. In this character they more resemble the specimens figured by Hoglund. The ventral sutures are also much straighter. It should be noted that the ventral side in our specimen is much more concave than would appear from the stereoscanner photograph. Although it might be objected that most species of Tvochammina show a star-shaped umbilicus (as, indeed, do species of Rosalina and Ammonia) the sutural fissures are particularly geometric in this form, as pointed out by Hoglund. DISTRIBUTION. This species was described by Rhumbler from Amphioxus Sand and Polygordius—Schill, Helgoland, Germany. MHoglund’s material is from the Skagerak and Kattegat. It is also listed from Plymouth (Murray, 1965a). Trochammina haynesi Atkinson (Text-fig. 6, nos I-3) Trochammina haynesi Atkinson, 1969 : 528, fig. 6, nos Ia-c. ? Tvochammina sp. Lutze, 1965 : 92, pl. 15, figs 21-23; pl. 12, figs 1 and 2. DiaGnosis. A concavo-convex species of Trochammina with six to nine chambers in the second whorl and final chambers becoming long and low. Umbilicus small with irregular sutural fissures. Early whorls with little agglutinated material, tectin dark brown. DESCRIPTION. (Paratype, Text-fig. nos 1-3.) Test concavo-convex, with sub- round, irregular, lobate periphery; chambers arranged in a sinistral, trochospire, 6:9:9: 2—, after the proloculus, very gradually increasing in size as added and _ becoming twice as long as high by the third whorl, as seen from the raised, evolute, dorsal side, sutures distinct, impressed, swept back; eight chambers visible on the J. R. HAYNES : 30 deeply concave, evolute, ventral side, umbilicus and aperture obscured, sutures sigmoid, impressed; wall of very fine, angular silt grains, first two whorls with very little agglutinated material, the dark brown tectin layer being very striking in dorsal view. 0.0 O.5mm. Fic. 6, 1-3. Trochammina haynesi. specimen described. 1, ventral view; 2, side view; 3, dorsal view. DIMENSIONS. Diameter 0:31 mm, height 0-15 mm. Proloculus diameter approx. 20 microns. MATERIAL. Paratype from K. Atkinson collection. Derosirory. B.M:(N.H.) Slide 1970 : 11 2 20 : 33. PROVENANCE. CB 417. REMARKS. Although slightly smaller, range of diameters given 0-15—0-2I mm, the specimens reported as Tvochammina sp. by Lutze appear to show the essential features of Atkinson’s species. DISTRIBUTION. This species was described from the littoral and sublittoral of Cardigan Bay where it was found associated with Dictyotaand Laminaria. Lutze’s specimens are from the Baltic, Ostsee. Trochammina globigeriniformis var. pygmaea Hoglund (Pl. 4, fig. 14) | Tvochammina globigeriniformis (Parker & Jones) var. pygmaea Hoglund, 1947 : 200, pl. 17, fig. 3; text-fig. 182. Diacnosis. A dwarf variety of T. globigeriniformis reaching up to about 0-25 mm in diameter. DEscRIPTION. (Pl. 4, fig. 14.) Test globose with convex sides and rounded periphery, lobate; chambers arranged in a sinistral, trochoid spiral, about 11 fol- lowing the proloculus, all visible on the evolute, dorsal side, only the last 34 on the involute, ventral side, longer than high and arcuate as seen on the dorsal side, CARDIGAN BAY RECENT FORAMINIFERA 27, inflated; sutures distinct, impressed; wall of very fine, angular silt grains (probably shell material) about Io microns in diameter in a neat, smooth, mosaic, parallel to the tectin base; aperture obscured but, apparently a ventral, basal slit (aperture of previous chamber possibly left open). Dimensions. Maximum diameter 0-24 mm. MATERIAL. One specimen only. ePOSirORY.. -B.M.(N.H.) Stub 1970 : 11:: 26.: 728. PROVENANCE. CB 408. REMARKS. The specimen described appears to fit well with the dwarf variety of Hoglund, distinguished by its small size from the much larger wae to 2 mm) and more stoutly built, 7. globigerintformis. DISTRIBUTION. This variety was originally recorded as a rare form in the Skagerak, and has also been noted by Murray at Plymouth (1965a); and in the Western Approaches (1970). Trochammina inflata (Montagu) (Pl. 4, figs 15-17; Pl. 6, fig. 3) Nautilus inflatus Montagu, 1808 : 81, pl. 18, fig. 3; Brown, 1844 : 1, pl. 1, fig. 4. Rotalina inflata (Montagu) Williamson, 1858 : 50, pl. 4, figs 93, 94. Trochammina inflata (Montagu) Carpenter, 1862 : 141, pl. 11, fig. 5; Brady, 1884 : 338, pl. 41, meswa—c. Goes, 1804 :-20, .pl. 6, igs 222-224; Cushman, 1944 : 17, pl.2, fig. 8; 1949 : 18, Des nes 3,43 Parker, 19052a : 407, pl. 4, igs 6 and:10; 1952b : 250, pl. 3; figs'1a, b; Todd & Low, 1961 : 15, pl. 1, figs 22, 23; Haake, 1962 : 30, pl. 1, figs 5 and 6; Loeblich & Tappan, 1964< : C250, fig.173, I DiaGnosis. A globose species of Tvochammina with five or six chambers in each whorl and radial sutures. Wall very finely arenaceous and generally red-brown in colour. DESCRIPTION. (Pl. 4, fig. 15, description of dorsal side based on additional specimen; Pl. 4, figs 16, 17.) Test globose, biconvex with raised ventral side and flattened dorsal side, periphery broadly rounded, lobate; chambers arranged in a dextral, low trochoid, spiral, with all the whorls visible on, the evolute, dorsal side, 14 chambers following the proloculus, 5 : 5 : 4—, in almost three whorls, moderately increasing in size as added, longer than high, rhomboidal, more than doubling in size with each volution, sutures radial, impressed, spiral suture angular; five cham- bers visible on the involute ventral side with radial sutures; wall of very fine silt grains about 3 microns in diameter, arranged in a neat mosaic parallel to the tectin base, inner lining of proloculus exposed, some minute openings between the grains _ less than a micron in size; aperture a slit at the basal margin of the final chamber on the ventral side, joining the small, deep, open umbilicus beneath a lip (obscured | by debris). : 38 J:-R. HAYNES Dimensions. Maximum diameter 0-60 mm, diameter of additional specimen shown in dorsal view 0-45 mm. Diameter of proloculus in this specimen about 25 microns. MATERIAL. More than 25 specimens. VARIATION. Specimens up to 0-70 mm maximum diameter were recovered. In Io specimens examined the proloculus diameter measured approximately 25 microns, with up to 16 chambers developed. Depository. 8B.M.(N.H.) Slide 19070 :.11 : 20: 41-43.- Stub “1970 ar > 26% 132-133: PROVENANCE. Station IIA, Clettwr Transect, Dovey Marshes, from High Marsh Sward. : ; REMARKS. This is a typical foraminifer of intertidal marshes and is adapted to lowered salinity and exposure. The chambers of the first whorl are often broken because of the delicate construction of the wall and the tectin lining may be exposed, a point referred to by both Williamson and Brady. DESCRIPTION. This species was described originally from the coast of Devonshire and it was recorded later by Williamson from both the English Channel and Skye, Scotland. Later records confirm a general near shore and brackish water distribu- tion around the British Isles: Irish Sea, Liverpool Bay (Pearcey, 1891) ; Dee Estuary (Siddall, 1875); Mersey Estuary (Burgess, 1891); West of Scotland, Firth of Clyde (Robertson, 1877); Western Isles (Heron-Allen & Earland, 1916a; Robertson, 1892) ; Shetlands (Waller, 1868); Forth (Pearcey, 1902) ; Northumbrian coasts and estuaries (Brady, 1865, 1870, 1884); English Channel, Christchurch (Murray, 1968); Selsey (Heron-Allen & Earland, 1909, I911); Exe Estuary (Worth, 1902); Plymouth and Cornwall (Heron-Allen & Earland, 1916b, 1930; Murray, 1965a; Worth, 1904); Western Ireland, Clare Island (Heron-Allen & Earland, 1913b). N.B. Williamson noted the rarity of this species in the sea. Such marine occurrences may be derived forms as suggested by Heron-Allen and Earland for the Selsey specimens which may come from Chichester Harbour and Bosham mud flats. Other N.W. European records include: Belgian coast (Cushman, 1949); Wadden Sea (Voorthuysen, 1951); Langeoog (Haake, 1962); Baltic (Goés, 1894). Mediterranean records include: Rhone Delta (Kruit, 1955). | Records for marshes and sounds in the Western Atlantic include: New York Bight (Ronai, 1955); New England (Cushman, 1944); Barnstaple Harbour (Phleger & Walton, 1950); New Hampshire (Parker, 1952a); Buzzards Bay (Parker, 1952b); Narragansett (Said, 1951); Great Pond, Massachusetts (Said, 1953); Poponessett (Parker & Athearn, 1959); Bay of Fundy (Harrington, 1955); Martha’s Vineyard (Todd & Low, 1961); Canadian and Greenland Arctic (Phleger, 1952); St Lawrence (Dawson, 1870). Gulf of Mexico and S.E. United States records include: Rappahannock Estuary, — Virginia (Ellison & Nichols, 1970); Mason Inlet, N. Carolina (Miller, 1953); North Gulf of Mexico (Phleger, 1960); Louisiana (Warren, 1957); Mississippi Delta (Lank- ford, 1959; Phleger, 1954, 1955); Texas coast (Lehman, 1957; Parker, Phieger@ Peirson, 1953; Phleger, 1956). =. a he “i ‘ a» Sie + } .. sg : CARDIGAN BAY’ RECENT: FORAMINIFERSA 39 South American records include: Southern Brazil (Boltovskoy, 1959); Argentina (Boltovskoy, 1961, 1963); Falklands (Heron-Allen & Earland, 1932). Pacific records include: general in Pacific coast marshes of N. America from Copper River Delta, Alaska to Mexico (Phleger, 1967); California (Bandy, 1963; Hanna & Church, 1927; Natland, 1933; Phleger, 1965; Walton, 1955); Sunset Bay, Oregon (Detling, 1958). Other Indo-Pacific records include: Malay Archipelago (Millett, 1899); off Japan (Cushman, I910); Oyster Harbour, Australia (McKenzie, 1962); Port Hacking, Australia (Albani, 1958); Manukau Harbour, New Zealand (Hulme, 1964). Antarctic records include: Weddell Sea and Falklands Sector (Earland, 1934) also Wiesner (1931). These records indicate a world wide distribution in extreme habitats, mainly intertidal, brackish water but also, apparently, including deep, cold water environ- ments. Trochammina intermedia (Rhumbler) ? (Pl. 4, figs 9-13; Pl. 6, fig. 9) Trochammina squamata intermedia Rhumbler, 1938 : 186, figs 27, a, b. Trochammina intermedia (Rhumbler) Hoglund, 1947 : 206, pl. 16, fig. 1; text-fig. 188. Tvochammina squamata Heron-Allen & Earland, 1913b: 50, pl. 3, figs 7, 8 only, cited by Rhumbler (not Jones & Parker). DiaGnosis. A concavo-convex species of Tvochammina with marked peripheral lobes on the ventral side and small to almost closed umbilicus. DESCRIPTION. (Pl. 4, fig. 9, description of dorsal side based on figs 12, 13.) Test with last chamber broken, concavo-convex, compressed, periphery subangular, _ lobate; chambers arranged in a low trochoid spiral of about three whorls, all visible _ on the raised, evolute, dorsal side, gradually increasing in size and becoming long and _ low with impressed swept back sutures, only the last five visible on the concave, _ involute, ventral side with marked lobes at the periphery; small, open umbilicus; wall of flat angular silt grains up to 20 microns diameter (probably shell material) neatly arranged parallel to the tectin base; aperture not visible. Dimensions. Maximum diameter 0-24 mm, additional specimen 0-17 mm. | MATERIAL. Four specimens only. VARIATION. Maximum diameters between 0-13 mm and 0:34 mm, Depository. B.M.(N.H.) Stub 1970 : II : 26 : 726-727, 734-735. - PROVENANCE. Specimens described Low marsh, Clettwr Transect Station VII, Dovey. Additional specimens figured, CB 13 and CB 33. REMARKS. Our specimens appear to show the characters of Rhumbler’s species but are much larger. In this respect they are nearer the specimens of Heron-Allen _ and Earland from off Clare Island. As noted by Hoglund the North Sea material _. shows the same chamber number in specimens only half the size or less which suggests a genetic difference. 40 J. R. HAYNES DIsTRIBUTION. The species was first described from Helgoland while Hoglund’s specimen came from the Skagerak. Heron-Allen and Earland found their specimens, ‘almost universally distributed (24 stations)’, off Clare Island, W. Ireland. Trochammina ochracea (Williamson) (Pl. 5, figs 15-18) Rotalina ochracea Williamson, 1858 : 55, pl. 4, fig. 112; pl. 5, fig. 113. Trochammina ochracea (Williamson) Balkwill & Millett, 1884 : 25, pl. 1, fig. 7; Cushman, 1920 : 75, pl. 15, fig. 3 (after Williamson); 1944 : 19, pl. 2, figs 12, 13; 1949: 17, pl. 3, fig. 1; Hog- lund, 1947 : 211, pl. 16, fig. 2; text-fig. 190; Todd & Low, 1961 : 16, pl. 1, fig. 18; Feyling- Hanssen, 1964 : 240, pl. 3, figs 11, 12; Hedley e¢ al., 1964 : 419, tab. 1, fig. 2, no. 2, fig. 3, no. 2 (syntypes). Trochammina ochvacea ochvacea (Williamson) Rhumbler, 1938 : 190. Diacnosis. A scale-like, concavo-convex species of Tvochamnmina with eight or nine chambers visible on the ventral side. Dark brown in colour with yellow, limbate sutures and irregularly asteroid umbilicus. DESCRIPTION. (Pl. 5, figs 15, 16, account of dorsal side based on additional specimen, figs 17, 18.) Test concavo-convex, thin and scale-like, periphery entire, subangular; about three whorls of chambers, all visible on the evolute, raised dorsal side, gradually increasing in size as added and becoming long and low, sutures slightly impressed; eight chambers visible on the concave, involute, ventral side; ventral sutures limbate, slightly raised, incised towards the open umbilicus making an irregularly asteroid figure, markedly flexuous; wall of very fine angular silt grains about 10 microns in diameter, arranged in a neat mosaic parallel to the tectin base; aperture apparently basal at the ventral suture of the last chamber communicating with the open umbilicus beneath the umbilical lobe; colour dark, resinous brown with light yellow septa. Dimensions. Maximum diameter 0-24 mm, diameter of additional specimen shown in dorsal view 0-16 mm, MATERIAL. Two specimens only. Depository. B.M.(N.H.) Stub 1970 : 11 : 26 : 736-737. PROVENANCE. Both specimens illustrated, Station VII, Clettwr Transect, Dovey Marshes. 3 | REMARKS. Our specimens fit well with the syntypes examined in the British Museum as well as with the accurate original description and the beautiful, coloured, type figures which show the dark test and ochraceous septa. These features are, of course, not seen in the stereoscanner photo which emphasizes the elevation of the sutures and the irregularly asteroid umbilicus. As shown by Hedley et al. the open umbilicus distinguishes this species from T. arctica (= T. squamata Parker & Jones, 1865). The last few chambers in our specimen show the tendency to develop lobes at the ventral suture which may indicate a gradation between this form and Remaneica helgolandica. CARDIGAN BAY. RECENT FORAMINIFERA AI DISTRIBUTION. This species was originally described from Skye, Scotland. Subsequent records for the British Isles include: Firth of Forth (Pearcey, 1902); West of Scotland (Heron-Allen & Earland, 1916a); Clare Island, W. Ireland (Heron- Allen & Earland, 1913b); Galway (Balkwill & Millett, 1884); Scillies (Atkinson, 1970); English Channel, Plymouth (Heron-Allen & Earland, 1930; Murray, 1965a); Western Approaches (Murray, 1970); Jersey (Halkyard, 1889); Belgian coast (Cushman, 1949). Records for the N.W. Atlantic include: New England, Buzzards Bay and Vineyard Sound (Cushman, 1944); Martha’s Vineyard (Todd & Low, 1961). It has also been recorded from the Late Glacial and Holocene of the Oslofjord area (Feyling-Hanssen, 1964) and from off the coast of Argentina (Boltovskoy & Boltovskoy, 1968). Genus JADAMMINA Bartenstein & Brand, 1938 Jadammina macrescens (Brady) (Pl. 1, fig. 5; Pl. 2, figs 14-16; Text-fig. 7, nos I-5) Trochammina inflata (Montagu) var. macrescens Brady, 1870 : 290, pl. 11, figs 5a—c; Cushman, mogzOn2 74, pl..15; fig. 1 (after Brady); 1949.: 19, pl. 3, figs 5, 6. Trochammina macrescens (Brady) Phleger & Walton, 1950 : 281, pl. 2, figs 6-9; Parker, 1952a : HOS, Pld, 185: 8a,-b; 1952b : 260, pl. 3, figs 3a,.b; Parker & Athearn, 1959 : 341, ‘pl. 50, figs 23-25; Todd & Low, 1961 : 16, pl. 1, fig. 16. Jadammina macrescens (Brady) Adams & Haynes, 1965 : 30 (list); Murray, 1965a : 503 (list). Jadammina polystoma Bartenstein & Brand, 1938 : 381, text-figs 1-3; Parker & Athearn, EO59)- 341,.pl.<50, figs 21,.22,.27; Haake, 1962 :.31, pl.1, figs 7-9; Feyling-Hanssen, 1964 : 241, pl. 3, figs 13-15; Brodniewicz, 1965 : 200, text-fig. 27. Driacnosis. A subglobular species of Jadammina with about eight chambers visible at the periphery and a variable number of small, round, areal apertures. 0.0 0.5mm. Fic. 7, 1-5. Jadammina macrescens. 1, specimen described, ventral view; 2, dorsal view; 3, apertural view; 4, apertural view of specimen with smaller proloculus; 5, ventral view of same. J. R. HAYNES DESCRIPTION. (Text-fig. nos 1-3.) Test slightly collapsed with damaged final chamber, subglobular with flattened sides, periphery rounded, semilobate; chambers arranged in a low, sinistral trochospire, 5 : 6 : 5—, following the proloculus; seven chambers visible on the involute ventral side with impressed, sinuous sutures meeting in a small, shallow umbilicus; 16 chambers visible on the evolute, dorsal side, eradually increasing in size as. added but slightly irregularly, becoming slightly higher than long at the end of the second whorl and showing a tendency to uncoil, septal and spiral sutures impressed, septal sutures backward curving, umbilicus wide and shallow; wall tectinous, golden brown with extremely fine agglutinated silt grains; apertures obscured, but apparently including a long, low opening at the be sal suture and at least two, round areal opcunes in the apertural face, each with a slight neck. DIMENSIONS. Maximum diameter 0-42 mm, height 0-13 mm. Diameter of proloculus approx. I5 microns. MaTertaL. More than 25 specimens, mostly collapsed but many apparently showing the original test shape although slightly damaged and distorted. VARIATION. Generally up to two and a half whorls are developed with five or six chambers in the first, six or seven chambers in the second. From 7—9 chambers are visible on the ventral side. A specimen with smaller proloculus than the speci- men described above is also illustrated. In this case the proloculus is about 10 microns in diameter and is followed by successive whorls with 6 : 7 : 5—chambers. This specimen reaches a maximum diameter of 0:34 mm (slightly distorted). Irena Brodniewicz illustrates specimens of almost the same size but with larger proloculus, about 20-25 microns in largest diameter and 11 to 12 chambers only. There is thus a strong indication of variation in chamber number connected with variation in proloculus size. The development of the areal apertures is also variable. DEPOSITORY. - B-M.(N.H.)’ Slide 1970 : 11: 26%. 33-40," Stub 10707 ee 20 628, 629. PROVENANCE. Specimen described and others illustrated, High Marsh Sward, Clettwr Transect, Station IIA, Dovey Marshes. REMARKS. The apertures are frequently obscured in this delicate species which is prone to collapse on drying or burial in sediment. As, in any case, the develop- ment of the areal apertures appears to be a variable feature it becomes merely an academic exercise to attempt to distinguish Tvochammina macrescens from Jadammina polystoma, After examination of the excellent material of Brady from Westport in the British Museum we agree with Parker and Athearn who suggested that these species were virtually identical. Bartenstein (1969) has recently shown how they see a very similar geographical range and morphology apart from the aperture detauls. Our stereoscanner photo shows very well the low basal aperture and the beautiful, masonic detail of the grains in the lips of the areal apertures (PI. 1, fig. 5). DISTRIBUTION. This species was originally recorded by Brady from brackish water, tidal rivers in Northumberland and Durham (Rivers Wear and Blyth) and ee * CARDIGAN BAY..RECENT FORAMINIFERA 43 from Loch Grunard and Loch Gilp, Scotland and Westport, Ireland. Later records confirm this distribution: Irish Sea (Balkwill & Wright, 1882, 1885); Mersey (Burgess, 1891); Dee (Siddall, 1878); Southport (Chaster, 1892); Western Ireland (Balkwill & Millett, 1884; Heron-Allen & Earland, 1913b). English Channel, Cornwall (Clarke, 1906; Heron-Allen & Earland, 1g16b, 1930; Murray, 1965a); Hampshire, Christchurch (Murray, 1968); Kent coast (Hedley - & Underwood, 1957); Western Scotland, Loch Hourn (Heron-Allen & Earland, 1916a). Northwest European records include: Belgium (Cushman, 1949); Holland and Germany, Dollart-Ems Estuary (Voorthuysen, 1960); Jade Bay (Bartenstein & Brand, 1938); Langeoog (Haake, 1962); Ostsee (Lutze, 1965); Poland, S. Baltic (Brodniewicz, 1965) as well as the Holocene of Oslofjord (Feyling-Hanssen, 1964). Records for brackish water areas and marshes in Eastern N. America include: New England, Barnstaple (Phleger & Walton, 1950); New Hampshire (Parker, 1952a) ; Martha’s Vineyard (Todd & Low, 1961); Poponesset Bay (Parker & Athearn, 1959); Long Island (Parker, 1952b); Staten Island (Behm & Grekulinski, 1958); Virginia, Rappahannock Estuary (Ellison & Nicols, 1970). Records for the Gulf of Mexico include: (Phleger, Parker & Peirson, 1953; Phleger, 1960); Galveston Bay, Texas (Phleger, 1965); Lagoa dos Patos (Closs, 1962). Records for the Pacific Coast include: California (Bandy, 1963; Phleger & Bradshaw, 1966); marshes from Mexico to British Colombia (Phleger, 1967). South American records include: Puerto Deseado (Boltovskoy, 1963). A general distribution in cool to warm temperate marshlands is indicated. Genus REMANEICA Rhumbler, 1938 Remaneica helgolandica Rhumbler (Piss; tie. 10;° PI 6;., fig: 6) Remaneica helgolandica Rhumbler, 1938 : 195, text-figs 38-45. Diacnosis. 608; 600, 1070: : Er 20 4752. PROVENANCE. Specimen described and also specimen illustrated in Text-fig. no. 5, Dovey Estuary, CB 156. Specimens illustrated Text-fig. no. 4 and by stereoscanner, CB: 8: REMARKS. As is shown by the tangled synonymy previous workers have found this species difficult to classify. In part this is because the original figures of Williamson do not show the supplementary chamberlets although they show the other characteristic features very well, including the coarse pores, ‘the marginal row of white foramina’. This led to confusion with Discorbina rosacea which on the basis of d’Orbigny’s model is a species without chamberlets and with distinct umbilical boss. This means that the attempt of Heron-Allen and Earland to divide the Clare Island population of A. mamilla into three species, including D. rosacea and D. planorbis on the basis of differences in test height is invalid. As shown above these variations are considered infraspecific as is the tendency to develop a keel. The presence of supplementary chamberlets excludes this species from Discorbis © and Rosalina and we follow Hofker in placing it in Asterigerinata. However, some doubt remains because the high arched aperture opening into the umbilicus and the rounded periphery in the young specimens indicate a relationship with Eoeponidella; possibly that genus is a Cretaceous-Palaeogene fore-runner of Asterigerinata. DISTRIBUTION. This species was originally described from the western coasts of Great Britain from the Shetlands to Bantry Bay and the Western Approaches of the English Channel. Later records confirm this distribution: Connemara (Alcock, 1865); off Jura and Ardnamurchan and in Loch Sunart, West of Scotland (Heron-Allen & Earland, 1g16a); Isle of Man (Heron-Allen & Earland, 1915; Bruce CARDIGAN BAY RECENT -.FORAMINIFERA 167 et al., 1963); Mersey (Burgess, 1891); Scillies (Atkinson, 1970); Plymouth (Heron- Allen & Earland, 1930; Murray, 1965a); Clare Island (Heron-Allen & Earland, 1913b); off Cork (Cushman, 1931); off Northumberland and Durham (Brady, 1867); Western Approaches (Le Calvez & Boillot, 1967; Murray, 1970). Other N.W. European records are: off Finistére (Dupeuble, 1963); Celtic Sea (Le Calvez, 1958); Dollart-Ems Estuary and Wadden Sea (Voorthuysen, Ig60, 1958); Belgian coast (Cushman, 1949); North Atlantic Cores (Parker et al., 1953). Mediterranean records are: Gulf of Naples (Hofker, 1951a) ; Western Mediterranean (Todd, 1958); Aegean (Parker, 1958); Tyrrhenian Sea (Norin, 1958); off Marseilles (Blanc-Vernet, 1958); Eastern Mediterranean (Parker, 1958). There is thus a marked concentration of records in the Mediterranean—Lusitanian province. It is also recorded dead from the Rio de La Plata (Boltovskoy, 1958). Family SIPHONINIDAE Cushman, 1927 Genus SIPHONINA Reuss, 1850 Siphonina georgiana Haynes n. sp. per 20; figs 15,00: Pl.-23) fig. 9: Pli- 33; fig. to) Siphomna tubulosa Heron-Allen & Earland, 1930 : 188, pl. 4, figs 62-64 (not Cushman). Siphonina reticulata? Cushman, 1931 : 68, pl. 14, figs ra-c; 1949 : 48, pl. 9, figs 5a—c (not Czjzek). Diacnosis. A biconvex, smooth species of Siphonina with relatively narrow, fimbriate keel and short apertural neck. IDesoRirTiON. - Holotype (Pl. 20, fig. 16; Pl. 23, fig.9;: Pl. 33, fig. ro.) ‘Test biconvex, with ventral side slightly more raised than the dorsal side, oval to almost circular in side view, entire, slightly compressed with narrow, fimbriate keel; about two and a half whorls of chambers visible on the evolute dorsal side arranged in a trochoid spiral, much longer than high and gradually increasing in size, five visible on the involute ventral side; sutures on dorsal side indistinct, flush, strongly back- wards curving, subradial on the ventral side; wall radial with coarse, round pores along the. septal sutures, double rows on the ventral side, smooth; aperture sub- round with short neck and frilled, everted lip, with an internal plate that partially closes the apertural opening on the ventral side and turns in to join the previous foramen, bearing a narrow lip on its free border. Dimensions. Maximum diameter 0-37 mm, height 0-17 mm. MATERIAL. Four specimens. Three additional specimens in the Plymouth collection of Heron-Allen and Earland, 1955 : Io : 25 : 99 : 200. _ VarRIATION. The paratypes are more equally biconvex than the type but con- _ sistently show five chambers on the ventral side. The dorsal side of a small paratype, 0-23 mm maximum diameter, is illustrated (PI. 20, fig. 15). The largest paratype Measures 0-35 mm Maximum diameter. 168 J. R. HAYNES Depository: _B.M.(N.H.) Slide “1970: 11 ; 26 :-287=288., (paratypes). Stulb 1970 »I1 : 26: 714 (holotype), 1970 :. 11 ; 26 ; 715 (paratype). PROVENANCE. Holotype, Brit. Mus. Core 16. Small paratype on stub, Brit. Mus. Core 13. Large paratype in slide, CB 503; small paratype in slide, off the Breaches, north of Wicklow Head. REMARKS. In 1931 Cushman referred a specimen of Siphonina from the Belgian — coast with question to S. reticulata although noting that it did not entirely fit with Czjzek’s Miocene species. Similar specimens were illustrated as S. tubulosa from Plymouth by Heron-Allen & Earland in 1930 and again as S. reticulata? by Cushman from the Belgian coast in 1949. Our specimens are identical with these (Cushman’s specimens being somewhat larger, 0-50 mm maximum diameter) and although they are few in number we feel justified in proposing a new name to cover them and the material from the English Channel. S. georgiana differs from S. reticulata in its smooth rather than ae surface - and in its less developed keel. It similarly differs from S. bvadyana, the Caribbean species, in its less developed keel and fewer rows of pores; the apertural neck is also better developed. SS. twbulosa Cushman has very well developed tubules extend- ing from the margin. DERIVATION OF NAME. Refers to provenance on the edge of St Georges Channel. DISTRIBUTION. This species was reported as occasional all round the south and west coasts of Britain by Heron-Allen & Earland (1930). Other records are: off Jersey (Halkyard, 1889); Belgian coast (Cushman, 1931, 1949). Chaster’s record of S. reticulata from Southport, North Irish Sea (1892) probably does not belong here as the figure shows a form nearer S. tubulosa, as noted by Heron-Allen and Earland. Family EPONIDIDAE Hofker, 1951 Genus EPONIDES Montfort, 1808 Eponides repandus concameratus (Montagu) (Pl. 18, figs 10-12; Text-fig. 33, nos 1-3) Serpula concamerata Montagu, 1808 : 160 (fide Williamson). Rotalina concamerata (Montagu) Williamson, 1858 : 52, pl. 4, figs 10r-103 only, not 104, 105. Pulvinulina concamervata (Montagu) Cushman, 1915 : 52, pl. 25, fig. 1. Pulvinulina vepanda Carpenter, Parker & Jones, 1862 : 311 (new name for Williamson’s speci- mens, not Fichtel & Moll). Pulvinulina vepanda var. concamerata (Montagu) Brady, 1884 : 685, pl. 104, figs 19a-c. Eponides vepanda var. concamevata (Williamson) Cushman, 1931 : 51, pl. 11, figs 4a—c (after Williamson). Rosalina isabelleana Le Calvez & Boillot, 1967 : 397 (list), pl. 1, figs 1, 2 (not d’Orbigny). Dracnosis. A heavily ornamented subspecies of Eponides repandus with six to seven chambers visible on the ventral side. CARDIGAN BAY RECENT:.;:FORAMINIFERA 169 DESCRIPTION. (Text-fig. nos 1-3.) Test large and robust, biconvex with raised, rounded, evolute dorsal side and rather flattened, involute, ventral side with deep pseudumbilicus, periphery with thick, blunt keel, entire to semilobate; approx. three whorls of chambers arranged in a low, sinistral trochospire, last two whorls visible on the dorsal side, the chambers gradually increasing in size and long and low, lunate in shape, septa swept back, limbate and raised; six chambers visible on the ventral side, septa limbate, flush, sutures radial to sinuous, incised (along distal edge of each septum) ; wall thick, radial and lamellar, finely perforate; aperture a low, arched opening along the basal suture of the last chamber towards the peri- phery, connecting with the pseudumbilicus by a long slit, with a prominent lip; dorsal chamber surfaces covered with small tubercles (occasional ones near periphery on the ventral side), the first whorl and proloculus being hidden by secondary calcite. DIMENSIONS. Maximum diameter 1-20 mm, height approx. 0-72 mm. MATERIAL. Rare in Cardigan Bay but common below 20 fathoms in St Georges Channel. More than 25 specimens but most are current worn with broken last chamber. VARIATION. ‘The material is not sufficiently well preserved for study of dimor- phism and this aspect must await further collection. Our specimens consistently show the characteristic heavy ornament on the dorsal side with tubercles also present near the periphery on the ventral side. The pseudumbilicus is a feature of well grown specimens, formed as the later chambers draw away from the centre. IDerosirory.. B.M.(N.H.) Slide 1970 : 11.: 26 : 297-299.. Stub 1970: 11: 20: Ore. 0.0 1.0mm. ‘Fic. 33, 1-3. Eponides repandus concameralus. 1, ventral view; 2, side view; 3, dorsal view, showing heavy ornament. 170 J. R. HAYNES PROVENANCE. Specimen described, St Georges Channel, CB 585. Specimens illustrated by stereoscanner, Brit. Mus. Core 16. REMARKS. This form was first described but not figured by Montagu, the first illustrations being given by Williamson. Wilhamson, however, included Rosalina globularis = R. anomala in his conception of the species so the figures apply only in part. Cushman (1931) ascribed the name to Williamson rather than Montagu and this was followed by Barker (1960) on the ground that Montagu did not figure his Serpula concamerata and its identity is problematical. Contrari- wise it can be maintained that as Montagu’s name is accompanied by a valid indica- tion and as Williamson clearly put his material in synonymy with Montagu’s species the name must be ascribed to Montagu. Under the Rules of Nomenclature we cannot have it both ways. If we want the advantage of following Williamson’s usage we must accept his view that Montagu’s material was the same. If we argue that it was different then a new name has to be found for Williamson’s material (as in the parallel case of Elphidium williamsont). The type description, despite some difficulties, can be taken to apply to Williamson’s figures, as well as ours. For instance, there is a tendency for the chambers, ‘concamerations’, to be of unequal size with the penultimate one often smaller than the antepenultimate. Further, we have taken this form live from hydroids in St Georges Channel which resembles its ‘natural habit’ according to Montagu, ‘fixed on Sertulariae’. The question now arises of the relationship of this form to Eponides repandus (Fichtel & Moll) as redefined on the basis of a neotype from the Bay of Naples by Loeblich & Tappan (1962). This neotype is much closer to Williamson’s form than the specimens traditionally placed in EF. repandus by authors following Brady (1884)—actually Poroebonides. However, the British material can be distinguished as including larger specimens with more chambers in the ‘last whorl’ (indicating a slower rate of chamber size increase) and heavier ornament. Incidentally, Todd (1965) figures an eight chambered form from the tropical Pacific but this is also distinguished by a ventral boss. Le Calvez & Boillot (1967) refer specimens identical to ours from the Western English Channel to Rosalina isabelleana d’Orbigny. D’Orbigny’s species was first described from the Falklands (1839c) and the type figures and description indicate a lobate, thin keeled form with conspicuous perforation and umbilical ornament. Confusion has probably arisen because Heron-Allen & Earland (1932) refigured d’Orbigny’s species on the basis of specimens close to E. vepandus concameratus because they supposed d’Orbigny’s figures “extremely unsatisfactory’. This was a dangerous assumptionto make without re-examination of the type material especially as our experience is that d’Orbigny’s figures (like Williamson’s) are generally accurate. DISTRIBUTION. Williamson’s material was from the Irish Sea, including White- sands Bay, Pembrokeshire, Belfast Bay and the Hebrides and Shetlands. It was also described from Scarborough on the east coast. This distribution with con- centration on the western side of the British Isles is confirmed by later records: Clare Island (Heron-Allen & Earland, 1913b); Connemara (Alcock, 1865); Porcupine Station AA, off Scotland (Brady, 1884); West of Scotland (Heron-Allen & Earland, i tO ect RIE OSI AETS SI OIE I OSE at HY pe CARDIGAN BAY RECENT FORAMINIFERA Lat rg16a); Mersey (Burgess, 1891); English Channel, Western Approaches (Le Calvez & Boillot, 1967); Finistére (? Dupeuble, 1963); Channel Islands (Halkyard, 18809); Bay of Biscay (Caralp, Lamy & Pujos, 1970). Norvang (1945) recorded it off Iceland and emphasized its Boreal and Lusitanian range. Family CIBICIDIDAE Cushman, 1927 Genus CIBICIDES de Montfort, 1808 Cibicides fletcheri Galloway & Wissler (Text-fig. 35 nos I-3) Cibicides fletchert Galloway & Wissler, 19 27 : 64, pl. Io, figs 8a-c; Adams & Frampton, 1965 : 58, pl. 5, fig. 11; Haman, 1966b : 69, pl. 7, eS 225,22: Diacnosis. A plano-convex, coarsely perforate Czbicides with marked boss in the ventral umbilicus, sharp periphery, limbate sutures and up to about ro chambers visible at the periphery. DESCRIPTION. Test with last chamber broken, plano-convex, with raised ventral side bearing a marked umbilical boss and flat dorsal side, periphery acute and entire becoming slightly lobate at the last few chambers; about two whorls of chambers arranged in a low sinistral, trochospire, ten visible at the periphery, slowly increasing in size; sutures strongly limbate, slightly curved on the ventral side, markedly swept back on the dorsal side; wall apparently granular, coarsely perforate; aperture periphero-dorsal beneath a lip, apertural face imperforate and making an obtuse angle with the ventral side of the chamber, centre of dorsal side obscured by slight thickening. Dimensions. Maximum diameter 0-31 mm, maximum height 0-14 mm. MATERIAL. More than 25 specimens, most with broken last chamber or chambers. VARIATION. Smaller specimens show only seven or eight chambers at the peri- phery. The umbilical boss varies in size and increase in the amount of thickening on the dorsal side gives a gradation to C. fletchert var. sachalinica. DerosirorRyY. B.M.(N.H.) Slide 1970: 11:26:300. Stub 1970: 11 : 26: 562, 563. PROVENANCE. Described specimen, Low Marsh, Clettwr Transect, Dovey Marshes. REMARKS. Our specimens come near to those illustrated by Galloway and Wissler although smaller, with fewer chambers developed, though often with larger umbilical boss and more limbate sutures. This species appears to be closely related to C. lobatulus from which it differs in its umbilical boss, slower rate of chamber size increase, with ten rather than eight in the second whorl, and coarser pores in equivalent sized chambers. The wall observed in crushed specimens is apparently optically granular (but see remarks on C. lobatulus). DIsTRIBUTION. The type specimens were described from the Pleistocene of California and it has also been described from the Pliocene of Russia (Vasilenko, 1954). Recent records are as follows: Pacific, California coast (Butcher, 1951; Bandy, 1953; Walton, 1955). 172 Ts EEAMAN ES North Atlantic, Iceland (Adams & Frampton, 1965); fjord in the Faroe Islands (Haman, 1966b). South Atlantic, Argentina coast (Boltovskoy, 1954, 1957). This would seem to indicate a cool temperate to cold water distribution. Cibicides fletcheri var. sachalinica Vasilenko (Pl. 21, figs 1, 2: Text-fig. 34, nos 1-3) Cibicides (Cibicidoides) fletchert Galloway & Wissler var. sachalinica Vasilenko, 1954 : 185, pl. 33, figs 2a—c. 2? Planorbulina akneriana Goés, 1894 : 89, pl. 15, figs 778, 779. Diacnosis. VARIATION. Specimens with flat dorsal side and angular periphery occur as well as some that are slightly raised like the one described with more rounded periphery. Most commonly nine chambers can be counted on the ventral side. A specimen which is damaged by boring is also figured (Pl. 21, figs 1, 2) which as well as a discrete, dorsal plug has excavated septal sutures and well developed lobes. Wall in crushed specimens apparently granular. DWerocmtory. —.M:(N.H.) Slides 1970": 15’: 26 :-301, ‘1970 :.11 : 26 : 302, 303. Suaitg70 711: 20: 505,500. PROVENANCE. Described specimen Holocene, Scrobicularia Clays, Borth. Other specimens illustrated CB 21, 28 and 57. REMARKS. Our specimens resemble C. fletchert var. sachalimica in size and shape but differ in developing up to 10 chambers in the ‘last whorl’, bigger plugs and coarse perforation on the ventral side. At Station CB 28 two specimens were recovered with similar plugs and hmbate sutures to C. fletcheri on the ventral side but with the dorsal sides slightly raised and evolute with thick, glassy secondary calcite rather than plugs. One of these specimens is illustrated for comparison as Czbicides species, (Text-fig. nos 4-6). The perforation is apparently finer in these forms and they also have a resinous brown coloration which may be indicative of reworking. DISTRIBUTION. Vasilenko described his variety of C. fletchert from the Upper Ieto@cene of the U.S.S.R. It has not hitherto been recorded in the Atlantic. but specimens recorded by Goés (1894) as Planorbulina akneriana may belong to the same group. Cibicides lobatulus (Walker & Jacob) (Pi. 20, figs 1, 2; Pl. 21, figs 3, 5, 6; Pl. 33, figs 1-7; Text-fig. 35, nos 4-10) Nautilus lobatulus Walker & Jacob, 1798 : 642, pl. 14, fig. 36. Truncatulina tuberculata = Truncatulina lobatula (Walker & Jacob) d’Orbigny, 1826: 279, MO! I, mod. 37. Tvuncatulina lobatula (Walker & Jacob) d’Orbigny, 1839b : 134, pl. 2, figs 22-24; (as ‘lobata’); 1846 : 168, pl. 9, figs 18-23; Parker & Jones, 1857 : 293, pl. Io, figs 17-21; Williamson, 1858 : 59, pl. 5, figs 121-123; Terquem, 1875 : 434, pl. 4, figs 2a—c (ascribed to d’Orbigny) ; Brady (part), 1884 : 660, pl. 92, figs ta—c only; Mills, 1900 : 150, pl. 11, fig. 38. Cibicides lobatulus (Walker & Jacob) Cushman, 1927a : 93, pl. 20, fig. 4; 1931 : 118, pl. 21, figs 3a-c; 1944 : 36, pl. 4, figs 27, 28; ? 1948 : 79, pl. 8, figs 14a-c; 1949 : 51, pl. Io, fig. 6; Parker, 1952b : 446, pl. 5, figs 11a; b; Colom, 1952 : 39, pl. 3, figs 23-25; Todd & Low, 1961 ; Peeoee2.e..'20; -Dupeuble, 1962!.: 197, pl. 1,-figs 1, 4; Haakej‘1962 : 44, pl. 4; figs 7-9: FPeyling-Hanssen, 1964 : 339, pl. 19, figs 1-3; Lutze, 1965: 105, pl. 15, fig. 38; Adams & Premupton, 1965, :58, pl..5, fig: 10; Haman, 1966b : 69,:pl. 7, figs 24-26; Murray, 1970 : 484, Wie 2S 13, 14. Planorbulina farcta Fichtel & Moll sp. var. (Tvuncatulina) lobatula (Walker & Jacob) Parker & Jones, 1865 : 381, pl. 14, figs 3-6; pl. 16, figs 18-20. Planorbulina lobatula (Walker & Jacob) Goés, 1894 : 88, pl. 15, fig. 774. Lobatula vulgavis Fleming, 1828 : 232. Heterolepa lobatula (Walker & Jacob) Gonzalez-Donoso, 1969 : 6, pl. 2, fig. I. Diacnosis. A plano-convex, attached species of Cibicides with about eight 1 See addendum. 174 je Re HAYNES chambers in the second whorl and distinct perforations on both sides. Ventral sutures swept back and impressed, meeting in a shallow umbilicus. The chambers increase markedly with each whorl to slightly more than double their size as seen in dorsal view and tend to become arcuate and lobate. A slight keel may be developed. | | DeEscCRIPTION. (Text-fig. nos 4-6.) Test plano-convex with flat, dorsal attach- ment side and moderately raised ventral side, periphery acute, becoming slightly lobate at the last three chambers, ventral side with shallow umbilicus; about two whorls of chambers arranged in a low, dextral trochospire, eight visible at the periphery and in ventral view, slightly more than doubling in size in the ‘last whorl’ as seen on the dorsal side and becoming arcuate and longer than high; sutures on the ventral side impressed and swept back in an even curve, meeting in a shallow umbilicus, sutures on dorsal side imbate and becoming markedly curved back between the last few chambers, thickened spiral septum also prominent; wall — bilamellar, weakly radial and densely perforated with pores up to 5 microns in diameter (see below); aperture periphero-dorsal beneath a lip extending back along the spiral suture. DIMENSIONS. Maximum diameter 0:33 mm, height 0-13 mm. Proloculus and initial chambers not clearly seen. MATERIAL. More than 25 specimens. Abundant but mostly rather small and often with broken last chambers. VARIATION. Most specimens recovered come near to the specimen described in their size but larger specimens occur some reaching more than I-o mm in maximum diameter. These tend to have six or seven chambers visible in the ‘last whorl’ and are more lobate, more distinctly perforated on the ventral side and flatter (Text-fig. nos 9, 10). Many of them show irregular coiling. Some specimens are rather higher on the ventral side and the last chamber may overlap the umbilicus. We illustrate a form with ventral umbo and nine chambers visible that seems to be intermediate with C. fletchert (Text-fig. nos 7, 8). Depository: ~B.M.(N.H.). -Slide~ 1970 :11 > 2679 334-243. “Section #1070. 26 : 484-490. Stub 1970 : II : 26 : 559-561. PROVENANCE. Specimen described, CB 534. REMARKS. Many authors such as McLean (1956), Hulme (1964) and Nyholm (1961) have lumped this species with others, such as C. refulgens Montfort. McLean went so far as to say ‘unfortunately, so many different forms have been ascribed to Walker and Jacob’s species that assigning the name “‘Jobatulus’” to a Cibicides is tantamount to giving the form a status more truthfully described by the term ~ “incertae sedis”. The species should probably be suspended as being of no taxo- nomic value—it was badly figured and inadequately described in the first place’. However, we regard these views as extreme and on our part we find C. lobatulus an abundant and easily distinguishable species in Cardigan Bay, closely comparable with populations occurring elsewhere off British coasts, both off Ireland and Scot- land, and consistently identified by previous authors. CARDIGAN BAY RECENT FORAMINIFERA 175 The specimen described comes very close to that figured by Williamson especially in the shape and regular increase in size of the chambers and in the appearance of the ventral sutures. As he noted, the shell is often glassy in the young state tending to become opaque in the adult. Larger specimens from Cardigan Bay come nearer to the type figures of Walker and Jacob which show a lobate form with six chambers on the ventral side with rather irregular increase in growth. We show a very similar individual with identical aperture on the dorsal side and which also has an incipient keel, a feature also mentioned by Williamson. The test is distinctly perforated on both sides with round to irregular pores, up to 5 microns in diameter on the dorsal side, cylindrical, often plugged and sometimes linking up in lines or clusters giving a frosted appearance to the test (Pl. 21, fig. 6). The pores are ir- regular in size and density and as shown in Text-fig. no. 10, where the dorsal side becomes thickened in large specimens considerable areas become poreless. The pores are equally dense on the ventral side but smaller, up to about 2 microns in diameter (Pl. 21, fig. 3). They are also funnel-shaped, widening to the exterior. It is possible that it is for this reason that younger tests appear more glassy on this side. Thin sections (Pl. 33, figs 1-7) of specimens from Cardigan Bay, Connemara and Moss Head, Scotland reveal that the chamber walls are weakly, optically radial and possess an inner lining separated from an outer lamella by a dark, probably organic, intervening layer; though in some cases and particularly towards the final chamber the dark layer cannot be readily distinguished from the outer layer (Pl. 33, figs 2-4) which probably explains why the wall appears optically granular in a simple crush (Adams, 1963). Hofker described this wall structure as trilamellar, believing the dark layer to be granular (1967) but it is more likely that it represents the original tectin layer. In this case the test can still be considered essentially bilamellar in the sense of Reiss (1959) and Hansen, Reiss & Schneidermann (1969). This structure is much the same as that shown by typical C. refulgens Montiort from Moss Head, Pl. 32, figs 6-g. The chief difference is that in Crbicides lobatulus the outer lamellae do not fully invest previous chambers in the adult part, the spiral cord remaining thin. In many cases the lamellae simply wedge out or merely abut previous chambers. This is consistent with the more spreading growth and ventrally umbilicate form in this species. The idea that the details of wall structure are specific only in this group is sup- ported by the structure of the closely related, possibly ancestral, Paleocene species C. cassivellaunit Haynes which is bilamellar but optically granular (Pl. 33, fig. 9). This is a plano-convex species which can be placed with, Cibicidotdes only on the basis of its granular wall. Conversely C. pseudoungerianus (Cushman), otherwise near Cibicidoides with coarse pores and raised dorsal side, is radial (Pl. 33, fig. 8, see also Wood & Haynes, 1957). This strongly indicates the possibility of progres- sive changes in wall structure at the specific level, as suggested by Haynes (1956) and Hofker (1967). N.B. According to Gonzalez-Donoso (1969) C. lobatulus is ‘pseudotrilamellaire’ and the dark layer is interpreted as the original primary outer wall. It is supposed that this layer is covered by an extension of the inner _ lining (analogous to a ‘septal flap’) when a further chamber is added. For this 0.0 0.5 mm. Fic. 35. .1-3. Cibicides fletcheri, Dovey. 1, side view; 2, ventral view; 3, dorsal view. 4-6. Cibicides lobatulus, CB 534. 4, side view; 5, ventral view; 6, dorsal view. 7, 8. Cibicides lobatulus, specimen intermediate with C. fletcheri, side and ventral views. 9,10. Large specimen of C. lobatulus with lobate periphery, incipient keel and strongly punctate ventral side and glassy, imperforate areas on the dorsal side. MM CARDIGAN BAY RECENT FORAMINIFERA 177 reason the species was transferred to Heterolepba. We donot follow this interpretation which may have arisen because of the difficulty of distinguishing the dark zone consistently.from the outer layer. In any case, even if the differences between C. lobatulus and C. refulgens were considered generic the name Tvuncatulina d’Orbigny, 1826 takes precedence over Heterolepa Franzenau, 1884, T. lobatula being the geno-. holotype. Thin sections of the other species studied have also been put on file: 1970 : 11 : 260: Agi (C. pseudoungerianus), 1970 : II : 26 : 492 (C. cassivellaunt). DISTRIBUTION. This species has been described from every latitude in both hemispheres but many of the records are suspect. For instance Brady (1884) gives an excellent illustration of the species from Vigo Harbour, Spain which was later used by Cushman (1927) to illustrate his conception of Cibicides. However, the other figures given by Brady, of specimens from the Pacific, are different. Also many of the British listed records may possibly include C. fletcheri. For this reason we restrict ourselves to well founded, illustrated, records for the North Atlantic. C. lobatulus was originally described from Whitstable, Kent, S.E. England and as shown by Williamson ‘abounds on all parts of the coast of Great Britain and Ireland .. . the dead shells . . . of common occurrence amongst the shelly shore sand’ More particularly it occurs, ‘lurking amongst the roots of Laminariae or . . . clustering round the large corallines, which it often does in vast numbers’. It occurs widely as a dead form in the Western Approaches (Le Calvez & Boillot, 1967; Murray, 1970). Other records for the North Sea area are: coast of Norway (Parker & Jones, 1857; Goés, 1894; Feyling-Hanssen, 1964); Langeoog (Haake, 1962); Ostsee (Lutze, 1965); Belgian coast (Cushman, 1949). North Atlantic: Eastern plateau, Hunde Islands and Baffin Bay—common to 78 fathoms, absent from abyssal depths (Parker & Jones, 1865); Greenland (Goés, 1894); Arctic including Iceland and Hudson Bay (Cushman, 1948); New England (Cushman, 1944; Parker, 1952a; Todd & Low, 1961); coast of Spain (Colom, 1952). These records indicate a generally shallow water distribution where shelter can be found in weeds; apparently the species does not occur living under estuarine con- ditions. Family PLANORBULINIDAE Schwager, 1877 Genus PLANORBULINA dOrbigny, 1826 Planorbulina distoma Terquem (Pl-20, figs 10-127, Pl, 21, figs.4, 7, 8; Text-fig. 36, nos 1, 2) Planorbulina distoma Terquem, 1876 : 73; 1877: 164, pl. 8, fig. 11 (duplicate of deuxiéme fascicule). Planorbulina vulgaris Williamson, 1858 : 57, pl. 5, figs 119, 120 (not d’Orbigny). Planorbulina mediterranensis Brady, 1884 : 656, pl. 92, figs 2, 3; Goés, 1894 : 91, pl. 15, fig. 786; Millis, £900 149, pl.:11, fig. 37;.Cushman, 1931-: 120, pl. 24, fig. 5 only; 1949 :°52, pl. 10, fig. 9 {not d’Orbigny). Diacnosis. A species of Planorbulina with relatively high, subinvolute ventral 178 Jo Re HAW NES side and subangular periphery. The initial part is like Czbicides for about two whorls and is followed by about six irregular whorls of chambers finally arranged in alternating rings (megalospheric form). The chambers tend to be almost square at first in dorsal view, up to three times as long as high later. | DeEscrIPTION. (PI. 20, fig. 11, account of pores and apertures on the dorsal side based on additional specimen Pl. 20, fig. 12.) Test presumed originally attached, plano-convex with raised, partially involute ventral side and flat, evolute, dorsal side, roughly pentagonal in outline, periphery semi-lobate, subangular; all the cham- bers visible on the dorsal side commencing with 14 arranged in a low, trochoid spiral of about 24 whorls, these being followed by about 30 chambers arranged in rings, the rings at first irregular but finally of regular alternations of five chambers each, chambers increasing slowly but irregularly in size, becoming longer than high and slightly overlapping, septa limbate but flush; alternating rings of chambers of the last part clearly seen in ventral view, inflated and overlapping with impressed — sutures, some with irregular, flap-like extensions along the sutures between previous chambers; wall radial, composite lamellar, densely perforated by pores between I~2 microns in diameter and widening to the surface on the ventral side, up to A microns in diameter with interleaved sieve plates on the dorsal side (there is a tendency for the distance between the pores to be about double their diameter) ; aperture multiple, small openings about 15 microns in diameter, with lips, each chamber with two at the periphery and two at the dorsal basal suture, lips tending to become tubular extensions, apertures also developed on the flaps along the sutures on the ventral side. DIMENSIONS. Maximum diameter 0-66 mm. MaTERIAL. More than 25 specimens. 0.0 0.5 mm. ic. 36, 1, 2. Planorbulina distoma, dorsal views of dextral, megalospheric specimens showing initial trochospiral part, drawn in xylene, thus wall thickness and chamber rounding exaggerated. Dorsal, sutural apertures seen when specimens dry, also small umbilical boss and dorsal aperture in spiral part of no. 1. = a | | | CARDIGAN BAY RECENT FORAMINIFERA 179 VARIATION. As shown by the text figures the chambers are irregular in arrange- ment and shape immediately following the trochoid initial part but are consistently longer than high in the later part. The outline tends to pass from trigonal through quadrangular-pentagonal to subcircular with growth. Proloculus diameters measured between 20 and 30 microns. DeposiTrory. B.M.(N.H.) Slide 1970 : 11 : 26 : 344-347. Stub 1970: 11: 26: 558. PROVENANCE. Specimens described, CB 480. Additional specimens figured Text-fig. 1, CB 15, fig. 2 from off Helmsdale, Scotland. REMARKS. Specimens hitherto identified as Planorbulina mediterranensis from around the British Isles show consistent differences from that species. D’Orbigny’s original figures and model show a large, much depressed form with marked ventral umbilicus and with chambers tending to remain higher than long, particularly on the ventral side. Recent illustrations of material from the Spanish Mediterranean coast by Schnitker (1969) confirm these original illustrations, particularly in regard to the wafer thin, subcarinate test, the ventral umbilicus and the high ventral chambers. Although the dorsal views show more elongate chambers than the originals another detail is added in that the sutures are shown to be markedly raised. The specimens in our material show only a slight ventral umbilicus as the chambers are more inflated on that side with the periphery subangular rather than acute. The chambers as seen from the dorsal side become longer than high much more quickly and the septa although limbate are flush, not raised. The chambers in the final rings as seen from the ventral side are markedly elongate. Fortunately there is a name available for the N.W. European species in P. distoma as Terquem’s illustration gives the ventral view of a quadrangular specimen very near to forms occurring in our material. As far as we can ascertain peripheral apertures are absent from the intial Czbicides- like portion. So in this respect this species resembles P. mediterranensis. It therefore differs from Schnitker’s N. Carolina shelf species ‘P. mediterranensis’ = Planorbulina polystoma, in this regard as well as in its subangular rather than rounded periphery; the ventral pores also continue right up to the edge. The initial part although Czbicrdes-like is brownish in colour and there seems little danger of confusing juveniles with well developed specimens of C. lobatulus. DISTRIBUTION. This species was first described from shore sands at Dunkirk. Material in the British Museum collections originally referred to P. mediterranensis but which belongs here includes specimens from the English Channel, Salcombe, Devon (Brady Coll.); Skye (Parker & Jones Coll.); North Sea, Budle Bay, River Blyth and Montrose Basin; S.W. Ireland, Valentia (Norman Coll.). If we accept Williamson’s citation of P. vulgaris then there are records for all round the British Isles from the Shetlands to Eddystone Lighthouse. Other N.W. European records include: Belgian coast (Cushman, 1931); Scan- dinavia (Goés, 1894); N. Atlantic, Porcupine Station 23, N.W. of Ireland (Brady, 1884) ; Western Approaches (Le Calvez & Boillot, 1967; Murray, 1970). Material in British Museum collections from the Mediterranean includes both P. 180 J. R. HAYNES mediterranensis, Crete (Parker & Jones Coll.); Sardinia (Brady Coll.) and specimens intermediate with P. distoma, Leghorn (Parker & Jones Coll.\; Delos (Heron-Allen & Earland Coll.). Similar intermediate forms occur with P. mediterranensis in the West Indies (Parker & Jones Coll.). It thus seems probable that the two species form a morphological continuum; with P. distoma s.s. typical of high latitudes. Specimens referred to P. mediterranensis in the Parker & Jones collections from the Indian Ocean and Pacific (Melbourne) are different from P. mediterranensis s.s. and show a ‘Caribeanella’ initial stage followed by rings of small round, inflated chambers. Planorbulina species A (Pl 5) ie LA Pl oe ie. <0) DESCRIPTION. Test probably originally fixed, apparently largely undamaged; irregular in outline; about 10 globular chambers visible showing no definite arrange- ment and apparently not increasing rapidly in size as added; sutures distinct and impressed; apertures two in number at base of the last formed chamber, at either side, round with slight lip and denticulate margin within; wall radial with coarse pores set in deep pits, the pores with interior plates; margins of the pits smooth and raised giving a reticulate appearance to the surface. DimENSIONS. Maximum diameter about 0-30 mm. MATERIAL. Six specimens. Deposirory. B.M.(N.H.) Stub 1970 : 11 : 26 : 517. PROVENANCE. Described specimen, Brit. Mus. Core 14. REMARKS. The twin apertures at the base of the last chamber and the coarse pores (about 6 microns in diameter) show the close relationship of this form to P. distoma. A further difference in addition to the irregular arrangement and globular shape of the chambers is in the well developed character of the pits, only slightly shown on the dorsal side of P. distoma. The pores are also larger. Family GLOBIGERINIDAE Carpenter, Parker & Jones, 1862 Genus BIORBULINA Blow, 1956 Biorbulina bilobata (d’Orbigny) (PI. 20, fig. 5) Globigerina bilobata d’Orbigny, 1846 : 164, pl. 9, figs 11-14. : Orbulina bilobata (d’Orbigny) Bronniman, 1951 : 135, text-fig. 3, nos. I, 2, 9, 10, 17, 19; text-fig. A, NOS 5,\6;:17, 183 Colomy-1952 2743, pl: 8, heszo, 27. Biorbulina bilobata (d’Orbigny) Blow, 1956 : 60, text-fig. 2, no. 16. Diacnosis. Sitveblus beccarii Todd & Low, 1961 : 18, pl. 2, figs 18, I9. Ammonia beccarii (Linné) var. batavus (Hofker) Murray, 1965a : 502 (list), pl. 1, figs 1, 1; 2, 2 (stereopairs). Diacnosis. A biconvex Ammomia generally flattened on the dorsal side with subangular to subround periphery, reaching 0-40 mm in average diameter in 2-3 whorls, with eight or nine chambers visible on the ventral side. A large plug (often divided) fills the ventral umbilicus and smaller granules line the deeply fissured septal sutures. The spiral suture is often raised on the dorsal side and divided in the last whorl with small openings at the junctions with the sutures. DESCRIPTION. (Text-fig. nos 1-3.) Test with broken final chamber; biconvex, about twice as wide as high, with subangular periphery, ventral side involute and more strongly raised than the evolute, rather flattened dorsal side, outline weakly lobate; chambers 26 (including proloculus) slowly increasing in size as added and arranged in a very low trochoid spiral, 6 : 7 : g : 3—, in each whorl following the proloculus, becoming slightly longer than high in the third whorl as seen in dorsal view; dorsal side extremely smooth and sutures flush; nine chambers visible on the ventral side with thickened, angular umbilical ends, sutures straight, deeply incised towards the umbilicus and lined by small, clear calcite bosses; umbilicus large and filled by a single prominent plug; last chamber broken so the typical ventral, basal Q.O0 0.5mm. Fic. 39, 1-4. Ammonia batavus. I—3, Specimen described; 1, ventral view; 2, side view; 3, dorsal view; 4, additional megalospheric specimen, dorsal view. 188 J. R. HAYNES and umbilical aperture is not seen but the areal foramen of the previous apertural face can be seen with a rudimentary toothplate just below it; wall radial and lamellar building up a thick spiral septum, finely perforate. . DIMENSIONS. Maximum diameter 0:56 mm, height 0-25 mm. Proloculus dia- meter approx. 20 microns. : MaTERIAL. More than 25 specimens. This is the dominant species in Cardigan Bay in the dead populations but so far has not been found abundantly in the living state. VARIATION. We have made a variation study of one hundred specimens. This confirms in general Hofker’s observation that A. batavus represents a member of the A. beccarit plexus with distinctive shape, ornament and growth rate. In brief A. batavus is smaller, with less angular periphery in the adult, develops fewer chambers and has a range of proloculus sizes that is smaller and only just overlaps © that of A. beccarvitz. Ventral ornament is also less developed. Our measurements show that the proloculus diameter in the Cardigan Bay population ranges from just less than Io microns up to 80 microns (compared to 4-54 microns in Hofker’s North Sea population) and confirm his finding that the larger the diameter the lower the total number of chambers. Thus we found one specimen with a proloculus just below 10 microns in diameter to have 32 chambers while the specimen with a proloculus diameter of about 80 microns had 16. The text figures show the marked acceleration in growth that is connected with increase in prolocular size. Text-fig. no. 4 shows that a specimen with a proloculus diameter of about 40 microns reaches a test diameter of 0-40 mm in two whorls (16 chambers) whereas in the specimen described with proloculus of 20 microns diameter a test diameter of 0:40 mm is reached in 24 whorls (20 chambers) and the first whorl is by comparison only half the size. Hofker has suggested that his material reveals at least three proloculus size groups—microspheric or B forms averaging about 6 microns; megalospheric AI forms, about 17 microns, and Az forms about 50 microns. On this basis our figured specimens would represent the AI and A2 forms. However, our material also shows specimens with much larger megalospheres so there may be a range of sizes without clear cut groups. Our material also shows that considerable variation in ornament occurs. In many cases the umbilical plug 1s divided and the spiral septum may be raised on the dorsal side. DeEpository. B.M. (N.H.) Slide 1970 : 11 : 26: 3690-378, 1070 :-11 : 260 ; 376— 380, 1970.11 2°26 : 381. “Stub, 1070): 11 yw ;-5a45nS, 510. PROVENANCE. Described specimen (and other specimens used in variation study) Brit. Mus. Core 16, Cardigan Bay. REMARKS. Both directions of coiling occur in our population (76 % anti-clockwise) and it is interesting that this was noted by Walker & Boys (1784) in the very earliest days of scientific investigations into the foraminifera when they coined the sub- specific name “perversus’ for left coiling specimens of what was probably A. batavus CARDIGAN BAY RECENT FORAMINIFERA 189 (Nautilus beccart perversus). However, no ventral view was given by them, or later by Montagu (1803) or Brown (1844). In any case through long disuse the name should lapse as a nomen oblitum. DISTRIBUTION. As this species has been confused with A. beccariz for a long period its distribution remains to be worked out. It is undoubtedly widely distri- buted around the coasts of the British Isles and in the North Sea. It has been well figured by Murray from Plymouth (1965a) and in addition Parker (1952) and Todd & Low (1961) figure specimens that may belong to it from the eastern seaboard of N. America. Ammonia limnetes (Todd & Bronniman) (PL 18; figs 7-9; Pl. ro, fig. 8; Pl: 30, fig..8; Text-fig. 40, nos 1-5) Streblus limuetes Todd & Bronniman, 1957 : 38, pl. Io, figs 4a—c. Rotalia beccavii (Linné) var. sobrina Parker, 1952b : 457, pl. 5, figs 7a, b (not Shupak). ‘Rotalia’ beccavvi (Linné) variant C, Parker, Phleger & Peirson, 1953 : 13, pl. 14, figs 29-30. Diacnosis. A thin walled, compressed Ammonia with flattened dorsal side and six to seven chambers visible on the ventral side with subangular to subround lobes filling the umbilicus. DEscRIPTION. (Test-fig.nos 1-3.) Test with last chamber broken off; compressed with flattened, evolute dorsal side and slightly raised, involute ventral side, periphery rounded and only slightly lobate in outline; chambers 17, arranged in a very low trochospire and increasing slowly in size as added, 6 : 7 : 3— in each whorl following the proloculus, becoming longer than high and lunate in the second whorl as seen in dorsal view; sutures flush on the smooth dorsal side; six chambers visible in ventral view with subrounded lobes filling the umbilicus, sutures impressed and deeply fissured towards the umbilicus, excavated behind the prominent lobes; the last chamber is broken so the typical ventral, basal and umbilical aperture is not seen but the oval, areal foramen of the previous apertural face is revealed; wall radial, PKG. 40, 1-5. Ammonia limnetes. 1-3, specimen described; 1, ventral view; 2, side view; 3, dorsal view; 4, specimen with lower chambers coming in earlier, dorsal view; 5, ventral view of another specimen. 190 J. R. HAYNES thin and finely perforated (sections show the wall is lamellar in this species). Dimensions. Diameter 0-32 mm, height 0-12 mm. _ Proloculus diameter approx. 20 microns. : MATERIAL. More than 20 specimens. Abundant in the Boreal sediments penetrated by the Borth Boreholes. VARIATION. No proloculus size groups could be discerned in our specimens and those measured were all near 20 microns. Most of the specimens recovered show between 2-3 whorls and reach about 0-30 mm in total diameter. This is just below the lower end of the size range, 0-32 mm to 0-42 mm, reported by Todd and Bronniman for their Trinidad population. Six or seven chambers are de- veloped in the second whorl and six are generally visible externally. Some speci- mens such as those figured (Text-fig. nos 4, 5) show larget, lower chambers coming in earlier. Depository. B.M.(N.H.) Slide 1970 : 11 : 26 : 382-385, Section 1970 : 11 : 20: 493... Stubs 1070 211 2:26 : 542,°543; 1070.2 mu = 2007 75m) PROVENANCE. Illustrated specimens, Holocene, Borth Borehole 2, D7. REMARKS. Our population although reaching smaller diameters is otherwise almost identical with that of Todd and Bronniman. This is well shown by a com- parison of the stereoscanner photomicrograph of one of our specimens (Pl. 18, figs 7, 8) with the type figures. It will be noted that in both cases the umbilical lobes appear pointed. Caution is necessary here because this appearance is exag- gerated by the oblique angle at which the lobes are set in ventral view and by their overlap. Pl. 10, fig. 8 shows a close-up of the final lobe almost at right angles to the observer and it is seen to be subround rather than pointed (shaped like a finger nail) with a shght, tuberculate flange, arched along the basal suture to reveal the aperture. The close-up also shows that the sutural fissures are lined with tubercles as in other Ammonza species, though these are not apparent using the optical micro- scope. This species is close to A. tepida but distinguished by its thin, translucent although brownish wall, flat dorsal side and accelerated growth rate with the chambers doubling in size with each whorl (as seen in dorsal view). The lobes also cover up the umbilicus to a greater extent. It is distinguished from A. perlucida by its less inflated chambers and again by its flattened dorsal side. Todd and Bronniman include ‘Rotalia’ beccarit variety C. Parker, Phleger & Peirson from San Antonio Bay and Parker’s Rotalia beccarii var. sobrina in their species although these authors did not give side views. These references are there- fore included here fide Todd and Bronniman. DISTRIBUTION. This species was first described from Mangrove swamps in Trinidad and is a common Caribbean form as well as (apparently) penetrating as far north as New England along the coasts of N. America. In Cardigan Bay it is much more common in the Boreal than in the present-day sediments. It therefore has a similar distribution to A. tepida. It also occurs abundantly in the Holocene of the Somerset Levels. CARDIGAN BAY RECENT FORAMINIFERA 19t Ammonia tepida (Cushman) (PL, 18, tig. 17; Pl. 30, fig.-7; Text-fig. 41, nos 1-7) Rotalia beccarii (Linnaeus) var. tepida Cushman, 1926 : 79, pl. 1; 1931 : 61, pl. 13, figs 3a-c. Rotalia beccarii var. B, Parker, Phleger & Peirson, 1953 : 13, pl. 4, figs 25-28. Stveblus beccavii var. tepida (Cushman) Bradshaw, 1957 : 1138-1147, text-fig. 1; Todd & Bronniman, 1957 : 38, pl. 10, figs 5-11. Streblus tepidus (Cushman) Bandy, 1961 : 17, pl. I, fig. 5. Ammonia tepida Brodniewicz, 1965 : 216, pl. 7, figs 3a-c. Dracnosis. A small Ammonia, generally less than 0-40 mm in diameter after three whorls, with rounded periphery and raised, low conical dorsal side. From six to eight chambers are visible on the ventral side with rounded umbilical lips. The umbilicus is open. DEscRIPTION. (Text-fig. nos 5-7.) Test biconvex, twice as wide as high with the dorsal side most strongly raised and conical, periphery rounded and entire; chambers 22 (including proloculus) slowly increasing in size as added and arranged in a low, dextrally trochoid spiral, 6 : 7 : 8, in each whorl following the proloculus, tending to become longer and lower in the third whorl as seen in dorsal view; sutures swept back and flush on the dorsal side; eight chambers visible on the 0.0 O25 mm. Pic. 41, 1-7. Ammonia tepida. 1, megalospheric specimen; 2, side view; 3, large speci- men; 4, large specimen side view; 5—7, specimen described; 5, ventral view; 6, side view; 7, dorsal view. 192 Vig ke Lae NONISS) ventral side with rounded umbilical lobes tending to cover the otherwise open umbilicus; sutures straight to gently curved, depressed and fissured towards the umbilicus and excavated behind each lobe; aperture ventral, basal and umbilical internal foramen areal, oval with small toothplate below it; wall radial, lamellar and finely perforate apart from apertural face and umbilical lobes; possibly minutely tuberculate in the umbilical region. DIMENSIONS. Diameter 0-32 mm, height 0-17mm. _ Proloculus diameter approx. I5 microns. MATERIAL. More than 20 specimens. Very abundant in borehole material from Boreal sediments in the Dovey Estuary. VARIATION. Specimens up to 0-40 mm in diameter occur (Text-fig. no. 3) but most specimens are nearer 0-30 mm. A range of proloculus sizes from 15-75 microns was noted and as in the case of A. batavus an increase in size of the proloculus is associated with a tendency to a decrease in total number of chambers, to 15 or less. Longer, lower, more lobate chambers also come in earlier (Text-fig. no. 1). How- ever, no definite size groups could be distinguished. As in other Ammonza species the umbilical area tends to be minutely tuberculate. This is not very apparent in the specimen fully described but is beautifully shown in the specimen illustrated by stereoscanner photomicrograph (Pl. 18, fig. 17). DeEposiTtory. B.M.(N.H.). Slide’ 1970 : 11 : 26-: 386-302. ) Section” 1970-2 same 20°--AQ4.” Stub 1070 2 1.20.2 520. PROVENANCE. Described and illustrated specimens, Holocene, Grey Silty Sands, Borehole 3, D8 (Boreal). REMARKS. Our specimens seem to fit well into the present concept of the species held by the authors quoted but doubt remains because the original description was not well illustrated and included the phrase ‘towards the umbilicus . . . the ends of the chambers extended to a point’. This would apply more to our species A. aberdoveyensis than to the group we are applying the name ‘tef:da’ which tends to have bluntly rounded umbilical lobes. However, these lobes overlap and do appear more pointed when half hidden and this is also the case with topotypes of Cushman’s species in the British Museum. In addition our population is closely similar to that illustrated by Todd and Bronniman and which like the types is from the Caribbean. The population discovered in San Antonia Bay by Parker, Phleger and Peirson and cultured by Bradshaw includes a majority of forms with six cham- bers visible ventrally and large megalospheres, again though, with large, rounded umbilical lobes. There is also doubt concerning the relationship of A. flevensis Hofker to A. tepida. This species appears to be very close in general morphology but on the evidence of the photographs of Irena Brodniewicz (1965) has a different rate of chamber increase size with ‘fine, sharp, prick-like spines’ in the umbilical area. DISTRIBUTION. This species was first described from Puerto Rico and is common in the Caribbean. It has been recorded from the Holocene of Poland by Brodniewicz and may have been widespread in northern latitudes in the Boreal. CARDIGAN BAY RECENT FORAMINIFERA 193 Genus BUCCELLA Anderson, 1952 Buccella frigida (Cushman) (Pl. 18, fig. 13; Text-fig. 42, nos I-5) Pulvinulina frigida Cushman, 1922 : 12 (co-types not figured). Eponides frigida Cushman, 1931 (part) : 45. Buccella frigida (Cushman) Anderson, 1952 : 144, figs 4a—c, 5, 6a—c; Loeblich & Tappan, 1953 : muaepl. 22, igs 2, 3; Voorthuysen, 1958 : 32,-pl. 24, figs 15a~c; Todd & Low, 1961 : 18, pl. 1, figs 24, 25; Haake, 1962: 44, pl. 4, figs 3-6; Feyling-Hanssen, 1964 : 337, pl. 18, figs 15-18. Buccella frigida (Cushman) var. calida Cushman & Cole, 1930 : 98, pl. 13, figs 13a-c; Cushman, nOsm 2 A7, pl. 10, figs 3, 4; 1944 : 34,'pl. 4, figs 19, 20; 1949 :.46, pl. 9, figs 1a—-c; Parker, 1952b : 450, pl. 5, figs 3a, b. DiaGnosis. A biconvex species of Buccella with broadly rounded periphery and generally with raised, rounded dorsal side. Most commonly in what is probably the megalospheric generation, there are 6: 7 : 3 or 4—, chambers in each whorl following the proloculus. DESCRIPTION. (Text-fig. nos 1-3.) Test biconvex with broad, shallow ventral umbilicus, flattened dorsal side and rounded periphery, apertural face oblique to the equatorial plane, semilobate; with ten chambers in a low, trochoid dextral spiral, 6 : 4—, following the proloculus, gradually but irregularly increasing in size and becoming longer than high and lunate in the second whorl, six visible on the ventral side; dorsal sutures distinct and slightly thickened, curving back to the periphery, slightly impressed in the last whorl, ventral sutures indistinct, radial, impressed; apertures not visible; wall finely perforate, ornamented on the ventral side with small granules that fill the umbilicus and sutural depressions and cover the lower part of _ the apertural face, coalescing at the centre to give the appearance of a small button- _ like plug. DimENnSIonNsS. Maximum diameter 0-20 mm, height o-r10o mm. _ Proloculus diameter approx. 32 microns. MATERIAL. Eight specimens examined. ry 2 5 De eee Pg eg 0.0 C.5 mm. Fic. 42, 1-5. Buccella frigida. 1-3, specimen described; 1, ventral view; 2, side view; 3, dorsal view; 4, side view, additional specimen; 5, dorsal view of specimen with high chambers. 194 Jao E AN NEES VARIATION. The specimens from Cardigan Bay are smaller than the types and appear to be juveniles with only one and a half whorls developed. There is variation in the height of the dorsal side, some specimens being bun-shaped (Text-fig. no. 4). Another specimen shows larger, higher chambers in the second whorl (Text-fig. no. 5). These variations are also shown in authors’ figures and Loeblich and Tappan illustrate a specimen with a pointed or conoidal dorsal side. DEPOSITORY.~— B.M.(N.H.). Slide 1070: 11 3°26 » 241-245.” Stub) 1070 21 > Z6= 540, 541. | PROVENANCE. Figured specimens, Clettwr Transect, Station VII, Dovey Marshes. REMARKS. We follow here the emended definition of the species made by Ander- son based on a lectotype chosen from Cushman’s co-types. Anderson’s figures also include as hypotype the holotype of Eponides frigidus (Cushman) var. calida Cushman & Cole. This means that sharp keeled specimens such as those illustrated by Cushman, actually copies of figures of Pulvinulina repanda Fichtel & Moll var. Karstent Reuss, Parker & Jones, 1865, must be given other names. Most references to Epomdes karstent probably indicate B. inusitata Anderson. Thin sections show that the test wall is built of radial laminated calcite perforated by small round pores a little less than a micron in diameter. The strong development of calcite granules on the ventral side is shown in PI. 18, fig. 13 extending to the periphery below the apertural face. DISTRIBUTION. The lectotype was recovered from 18-3 metres in a bay near Black Whale Harbour, Canadian Arctic. This cold water occurrence has been generally confirmed by later discoveries such as those of Loeblich & Tappan (1953) and Vilks (1969). It occurs widely in cool temperate waters of the Western Atlantic and sparingly near the British Isles: Plymouth (Murray, 1965a); Christchurch (Murray, 1968); Bay of Biscay (Caralp, Lamy & Pujos, 1970) and in the North Sea area (Haake, 1962). Pleistocene references are given by Feyling-Hanssen (1964) and Voorthuysen (1958). A record for the Pacific coast of Japan is given by Matoba (1970). Family CASSIDULINIDAE d’Orbigny, 1839 Genus CASSIDULINA dOrbigny, 1826 Cassidulina cf. reniforme (Norvang). (Text-fig. 43, nos 1-4) Cassidulina crassa d’Orbigny var. veniforme Norvang, 1945 : 41, text-figs e-h; Cushman, 1948 : 75, pl. 8, figs 1oa—c (figures-after Norvang). DESCRIPTION. (Text-fig. nos 1-3.) Test slightly compressed with broadly rounded periphery, reniform in outline; chambers arranged in a_planispirally wound alternating, biserial series, three and a half pairs visible in the last whorl, the chambers extending over the umbilical region one side while extending one-third of the way to it on the other; sutures straight to slightly curved, flush; wall granular, \ CARDIGAN BAY RECENT FORAMINIFERA 195 distinctly and densely perforate; aperture countersunk, a short, curved slit, oblique to the basal suture, joining it at the junction with the basal suture of the previous chamber, bearing a flat tooth on the proximal side. Dimensions. Maximum diameter 0-13 mm, height 0-6 mm, MATERIAL. Twelve specimens only, most of them with the last chamber broken. VARIATION. Specimens occur with four pairs of chambers visible and up to 0-22 mm in diameter. Depository. B.M.(N.H.) Slide 1970.: 11 : 26 : 393-397. PROVENANCE. Described specimen Cardigan Bay, Brit. Mus. Core 14. REMARKS. This is the only species of Casstdulina we have so far recovered in any numbers in Cardigan Bay. The specimens are extremely small (possibly juvenile) and the details of the test consequently rather difficult to make out. Although smaller, about half the size, they are very close to Cassidulina crassa var. reniforme Norvang inshape and chamber form. They differ in that the aperture appears to be oblique to the basal suture rather than developed along it as in Nor- vang’s fig. h. In this regard our specimens more resemble Islandiella islandica (Norvang) but the tooth does not appear to protrude in our specimens and the wall is granular (two crushed specimens examined in polarized light). Norvang referred his new variety to Cassidulina crassa d’Orbigny but this is untenable. The original description and the later redescription of Heron-Allen & Farland (1932) from d’Orbigny’s collection in Paris and additional Falkland Islands material show that C. crassa is a large species, up to 1 mm diameter with five pairs of chambers and aperture almost at right angles to the basal suture. Apparently similar forms in the northern hemisphere were distinguished as C. obtusa by William- son (1858) who, with his usual accuracy, figures the aperture as a long slit, parallel to the periphery, as in C. laevigata. There seems little doubt that many of the 0.0 0.3 mm. Fic. 43, 1-4. Cassidulina cf. veniforme. 1, side view showing aperture; 2, oblique peripheral view; 3, view of reverse side; 4, foramen of broken specimen, apparently with areal branching. 196 jJ..R. HAYNES North Atlantic references to C. crassa such as those of Brady (1884), Goés (1894), Cushman (1922) and Norvang (1945) refer to C. obtusa. Similarly C. laevigata sensu Heron-Allen & Earland (1930) is C. obtusa. Norvang’s variety differs from C. obtusa in its shape and in its flush sutures as well as in the form of the aperture and should probably be regarded as a distinct species. The specimens described as Cassidulina laevigata d’Orbigny var. crassa d’Orbigny by Parker & Jones (1865) - may be the same as ours, as the figures show a short, oblique aperture and they remark significantly, ‘on the eastern plateau of the North Atlantic it is very rare and very small’. However, it is possible their figures are of a broken specimen and show the foramen of the previous chamber rather than the aperture. The foramen may differ from the aperture, even, apparently, showing areal branching as in our Text-fig. no. 4. Care must, therefore, be taken with broken specimens, especially before we know anything of the ontogenetic development of the aperture in Cas- sidulina species. Family NONIONIDAE Schultze, 1854 This family is interpeted in the wide sense to include both Nonion and Elphidium. Changes in wall structure are progressive and advanced forms tend to be optically radial. However, this feature cannot be used as the basis for subfamily division as In many cases it is demonstrably of specific importance only. Again, although Loeblich & Tappan (1964a) have recognized a number of genera in the Elpmdium group we continue to interpret this genus in the wide sense of Wade (1957) and earlier workers. This is because we still do not know enough about the strati- graphical relations of the species to decide what characters are important at the generic level. Two of our species, E. magellamicum and E. asterotuberculatum, are apparently primitive in possessing open sutural canals or irregular canal openings only. These appear close to Protelphidium on the one hand and Elpidiella on the other. FE. cuvilliert, E. selseyense and E. waddensis show coarse pores, irregular septal pits and bars and questionable retral processes. On this basis they could be grouped with Cribronomon. Except that some specimens of E. selseyense show areal apertures which alternatively suggest Cribroelpbhidium. E. incertum 1s finely perforate with incipient fossettes. The other species appear to fall into Elphidium s.s. but E. exoticum is optically granular, as is EF. incertum. Apparently, we are dealing with a plexus of species that has arisen from within the Nonion group, showing a general tendency towards development of radial walls and closed septal canals which then find an exit through regular fossettes with attendant enlargement of the septal flap and strengthening by septal bars. As evolution does not occur at a steady rate and we may be dealing with many lines we should not expect a particular species to be necessarily ‘advanced’ in all its characters. Thus, E. exoticwm is optically granular but has regular fossettes and advanced retral processes that communicate to the exterior via the proximal end of the septal bar. We therefore feel it to be unwise to multiply the number of generic names at present. CARDIGAN BAY RECENT FORAMINIFERA 197 Genus ELPHIDIUM Montfort, 1808 Elphidium asterotuberculatum (Voorthuysen) (Ply 22; fig: 7) Nonion depressulus (Walker & Jacob) forma asterotuberculata var. Voorthuysen, 1958 : 28 pmezomes 34a, b; 1960 : 254, pl. 11, fig. 21; Haake, 1962 : 41, pl. 3, fig. 5; ? Feyling-Hanssen, mQO4 2330, pl. 17, figs 13, 14. Cribrononion asklundi Lutze, 1965 : 105, pl. 15, fig. 42 (not Brotzen). Dracnosis. A compressed species of Elpiidium with high chambers and flat sides. The sutures are widely excavated but together with the umbilicus are closed by calcareous material giving a star-shaped figure. Septal canal openings small and irregular. | DESCRIPTION. Test with last chamber broken, compressed, circular in outline, periphery rounded, entire; chambers arranged in a planispire, seven to eight visible, slowly increasing in size, higher than long and higher than wide in apertural view; sutures broadly excavated and widening to the umbilicus, filled with calcareous material and small tubercles; openings of septal canals small and irregular with no development of true fossettes and bars; wall apparently radial, minutely perforate; no aperture but foramina multiple and basal. DIMENSIONS. Maximum diameter 0-20 mm, width approx. 0-05 mm. MATERIAL. One specimen. | Darosimmory. 6:M.(N.H.) Stub 1970 : 11 : 26 :. 685. PROVENANCE. Clettwr Transect, Dovey Marshes. REMARKS. This species was first described as a variety of N. depressulum = P. anglicum. It differs from that species in its more flattened form, more excavated sutures and in its closed septal canals with irregular openings. The tubercles tend to be restricted to the sutures and umbilicus. DISTRIBUTION. This species was described from the Eemian of the Netherlands but has also been recorded from the Recent at the following European localities: Netherlands, Dollart-Ems Estuary (Voorthuysen, 1960); Germany, Langeoog (Haake, 1962); Baltic, Ostsee (Lutze, 1965). Also from the Holocene of Oslofjord (Feyling-Hanssen, 1964). These last are more inflated than the types and resemble _ our material from the Holocene (Boreal) at Borth. Elphidium cuvilliert Lévy (Pl 24, figs 17,.18; Pl. 26, fig. 12) | Elphidium cuvillieri Lévy, 1966 : 5, pl. 1, fig. 6. Cribrononion cuvillieri (Lévy) Lévy et al., 1969 : 93, pl. 1, figs roa, b, 117. | Driacnosis. A compressed species of Elphidium with conspicuous round to oval septal pits and umbilicus closed with a perforate, glassy plate formed by the fused } ends of the chambers. | | 198 J. R. HAYNES DESCRIPTION. Test compressed with slightly depressed, closed, umbilical areas, periphery rounded, entire to semi-lobate at the last few chambers; chambers ar- ranged in an involute planispire; ten visible on the exterior, gradually increasing in size, septal sutures not visible but marked by well developed round to oval septal pits marking the surface expression of the internal septal canals, up to seven on each chamber, septal bridges (? internal retral processes) becoming bar-lke only — on last two chambers; wall apparently radial, densely perforated with fine to medium sized pores up to 2 microns in diameter, these pores absent from the umbilical areas and the apertural face, umbilical plate with scattered septal pits (and possibly the openings of umbilical canals), up to 10 microns in size, aperture a series of irregular openings along the basal suture of the last chamber. DIMENSIONS. Maximum diameter 0-47 mm, approx. width o- H mm, MATERIAL. One specimen only. Depository. B.M.(N.H.) 1970: 11 : 26: 604. PROVENANCE. Described specimen, CB 4ITI. REMARKS. Our specimen appears to be identical with the holotype in its pitted umbilical areas, in the size and distribution of the septal pits and in its perforation. This species can easily be overlooked because in certain lights the umbilical pits can appear to be umbilical bosses. DISTRIBUTION. This species was described from Roussillon and from the shore sands of Dunkirk in France. Elphidium exoticum Haynes n. sp. (PI. 24, figs 8, 9; Pl. 26, figs 2) 3, 6, 8: Pl 28;nes 1-4) DiaGcnosis. A compressed species of Elphidiwm with pearly, transparent granular wall and wide, flat umbilicus. Developing up to seven fingernail-shaped septal pits (fossettes) on each side of the final chambers and bar-like septal bridges. DESCRIPTION. (Holotype, Pl. 24, figs 8, 9; Pl. 26, figs 2, 3, 6,8.) Test compressed, rather flattened with wide flat umbilicus depressed below the level of the chamber sides, periphery subrounded, semilobate and slightly irregular; chambers arranged in an involute planispire, 11 visible externally, gradually increasing in size; sutures curved back to the periphery with well developed fingernail-shaped septal pits, narrow septal bars marking internal retral processes about one-quarter of the chambers in length, in some cases open proximally, especially on the last chamber” umbilicus filled with a flat plate formed by the fused ends of the earlier chambers, last five chambers with rounded, fissured, lobes drawn slightly away from the umbilicus; wall thin, granular, transparent with pearly lustre, densely perforate with fine pores less than 4 micron in diameter; aperture a series of small, round, hooded, openings at the eal suture of the last chamber: sharp spines line the sere pits and there are rather sparse tubercles at the base of the apertural face. | | } | | | CARDIGAN BAY RECENT FORAMINIFERA 199 DimMENnsIONS. Maximum diameter 0-38 mm, maximum width approx. o-Io mm. MaTerRIAL. More than 25 specimens. VARIATION. Specimens develop 10 or 11 chambers in the second whorl and apparent variation in the material from 7 to 11 is largely due to differences in growth. In two specimens cut the following measurements were obtained: Total diameter Proloculus diameter chambers in each whorl 0-29 mm 35 microns 7>IliI—, 0-26 mm 30 microns 7:10 :I—, Both specimens presumably belong to the megalospheric generation. The specimen described is larger than these, presumably with more than 2 whorls. Most specimens in the material appear to show less than two whorls. The paratypes show an average of nine chambers visible externally. Deposirory. B.M.(N.H.) Shde 1970 : 11 : 26 : 398-406 (paratypes). Sections, Me7Orerl 202495, 1970: 11 : 26: 496, 1970: 11 : 26: 497 (paratypes).~ Stub TQ70 : 11 : 20 : 596 (holotype). PROVENANCE. Holotype CB 156, Dovey Marshes. Paratypes CB 411, Tremadoc Bay. REMARKS. This species is distinguished from EF. discotdale (d’Orbigny) by its flat, non-pitted umbilical areas, flat sides, fewer chambers and fewer pits, also by its pearly, minutely perforate wall. The wide, flat umbilicus also distinguishes this species from EF. poeyvanum (d’Orbigny) and E. articulatum (d’Orbigny). The open retral processes are very distinctive in this species but they have been noted in E. williamsoni as well. DERIVATION OF NAME. Refers to the fact that this species has a beautiful, optically granular, wall—one of only two amongst the Elp/idium species recovered trom Cardigan Bay. Elphidium incertum (Williamson) (Pl 22, fie.°6; Pl.24; figs 14-16;: Pl. .28,: figs 8, 9) Polystomella umbilicatula var. incerta Williamson, 1858 : 44, pl. 3, fig. 82a. _ Elphidium incertum (Williamson) part Cushman, 1930: 18, pl. 7, fig. 4a only (figure after Williamson); 1948 : 56, pl. 6, figs 7a, b; Brodniewicz, 1965 : 207, pl. 10, figs 9-11; text-figs 30, 31; Buzas, 1966 : 593, pl. 72, figs 1-6. Cribrononion incertum (Williamson) Lutze, 1965 : 103, pl. 21, figs 43, 44. Elphidium voorthuyseni Haake, 1962 : 51, pl. 5, figs 6, 7. Elphidium varium Buzas, 1965 : 21, pl. 2, fig. 7; pl. 3, figs 1, 2 hee Diacnosis. A thin walled, granular, compressed species of Elphidium with flat sides, prominent sutural slits and only partial development of septal bars. The | septal openings tend to remain elongate in the line of the septa and there is little ————<—=—= = | development of true fossettes until the last few adult chambers. } “Hh 200 J. R. HAYNES DEscRIPTION. (PI. 24, figs 15,16.) Test compressed with flat, slightly umbilicate sides, umbilicus closed by the fused ends of the chambers, later chambers with- drawing slightly from the centre producing a pseudumbilicus, periphery rounded and entire; chambers arranged in an involute planispire, 11 visible externally, slowly increasing in size; sutures swept back in an even curve to the periphery, deeply excavated with irregular development of bars, true fossettes and retral pro- cesses not developed until the last few chambers; wall thin, optically granular and densely perforated with pores less than I micron in diameter; aperture a series of irregular openings along the basal suture of the last chamber, partly hidden by tubercles which also line the excavated sutures. DIMENSIONS. Maximum diameter 0-22 mm, maximum width 0-09 mm. MATERIAL. Eleven specimens, most of them small. VARIATION. The number of chambers visible externally ranges from eight in juveniles (Pl. 24, fig. 14) to Ir in well grown specimens. A thin section (Pl. 28, fig. 8) reveals a proloculus diameter of 20 microns and 7 : 9 : g—, chambers in successive whorls. DEPosIToRY. B.M:(N.H.) Slide 1970 : 11.: 26: 407, 408. Section 1070 > ieee 20 : 408... Stubs 1970 2 1h ; 207007, O70: IL = 20), Ooo: PROVENANCE. Specimen described and additional specimen illustrated, Clettwr Transect, Dovey Marshes. REMARKS. As noted by Loeblich & Tappan (1953) this characteristically thin walled, glassy species has been confused with a number of others in particular with the coarsely perforate, umbonate species, FE. clavatum Cushman. The Williamson Collection in the British Museum includes seven specimens of F. incertum put on a separate slide as ‘paralectotypes’ by Loeblich and Tappan. One of these specimens was examined by Buzas (1966) and found to be optically granular. This character together with the sutural slits and depressed umbilicus without a boss led him to place his own species, EF. vavium, in synonymy with it. We have made a thin section of another ‘paralectotype’ and our observations confirm those of Buzas. It is probable, also, that EF. voorthuyseni of Haake belongs here, as a topotype, kindly sent by Dr Haake, seems virtually indistinguishable. Our specimens, like the types, are rather small. Buzas gives a mean diameter of 0-36 mm for his population but specimens over 0-50 mm occur. Large specimens also occur in the Baltic population very well figured by Brodneiwicz. Two of her illustrations show sectioned specimens with proloculus diameters between 40- 60 microns, possibly near the upper limit of the megalosphere size range. DISTRIBUTION. Williamson found this species to be ‘prevalent’ only at Scar- borough on the North Sea coast; it has also been figured by Murray (1968) from Christchurch. Other records include: Baltic (Brodniewicz, 1965; Lutze, 1965) as well as a number in the N.W. Atlantic: Long Island Sound (Buzas, 1966); Hudson Bay (Cushman, 1948). These records indicate a temperate to cold water habitat. It occurs live on the Dovey Marshes. CARDIGAN BAY RECENT. FORAMINIFERA 201 Elphidium macellum (Fichtel & Moll) (Pl. 24, figs 1-3; Pl. 25, figs 1-5, 7, 8; Pl. 27, figs 4, 5) Nautilus macellus Fichtel & Moll, 1798 : 66, var. 8, pl. Io, figs h—k. Elphidium macellum (Fichtel & Moll) Montfort, 1808 : 15; Cushman & Leavitt, 1929 : 18, pl. 4, figs 1, 2; Cushman, 1939 : 51, pl. 14, figs 1-3; pl. 15, figs 9, 10; Feyling-Hanssen, 1964 : 347, ple 20, fig. 16. Polystomella macella (Fichtel & Moll) var. aculeata Silvestri, 1901 : 45. Elphidium macellum (Fichtel & Moll) var. aculeatum (Silvestri) Cushman, 1949: 27, pl. 5, fig. 10. Elphidium crispum (Linné) subsp. spinosum Atkinson, 1969 : 537, fig. 6, figs 4a, b. Diacnosis. A slightly keeled species of Elphidium with up to about 20 chambers visible and flat umbilical areas filled with the irregular, embossed ends of the cham- bers. Diameter usually less than I mm. Keel often spinose in the juvenile part. DESCRIPTION. (PI. 24, fig. 1; Pl. 25, figs 2-5, 7,8.) Test compressed, lenticular, sub-carinate, entire becoming slightly lobate at the last few chambers; numerous chambers arranged in an involute planispire, 17 visible at the exterior, increasing in size very slowly; sutures raised and strongly reflexed towards the periphery, with a row of narrow septal pits (fossettes) separated by bar-like septal bridges, representing retral processes almost equal in length to the chamber width, the pits which lead into the septal canals lined with spines, 14 pits on each side ot the last chamber; less than 12 in early whorls; wall radial, very finely perforate, larger pores (small pits?) in umbilicus; aperture consisting of irregular openings along the base of the last chamber linking up with the pits of the first visible chamber below, apertural face concave in the median line with rounded tubercles; umbilicus filled with the rounded, irregular ends of the chambers, large perforations surrounded by spines between. DIMENSIONS. Diameter 0-72 mm, width approx. 0-27 mm. MATERIAL. More than 25 specimens, all growth stages. _ WARIATION. Two specimens cut show proloculus diameters near 70 microns and are presumed megalospheric. One of these, illustrated Pl. 27, fig. 5, is about 0-7 mm in diameter and shows g : 18 : 5—, chambers in each whorl following the -proloculus, with twenty chambers visible at the periphery. The chambers giadually become higher. It is noteworthy that the second chamber is rounded as in Num- mulites. These specimens are beautifully radial in wall structure. Juveniles tend to bear spines at the periphery, usually as a continuation of the | septal suture, in some cases double or treble (Pl. 24, figs 2, 3). DePosirory. B.M.(N.H.) Slides 1970: 11 : 26 : 409-413, 1970: 11 : 26: 414 \Guvenile). Stub 1970: 11 : 26 : 593-595. Sections 1970 : II : 26: 499, 1970 : |e 26: > 500. PROVENANCE. Specimen described, CB 742. Specimens cut (Pl. 27, figs 4, 5), |B 37. Spinose juvenile, Holocene, Scrobicularia Clays, Borth. | REMARKS. As pointed out by Cushman & Leavitt (1929) the name of this species las often not been used in the original sense. Paucity of records around the British Ht : } | 202 Ifo Ike BUA VEIN ISS coasts probably indicates confusion with E. crisbum which is larger and has pitted umbilical bosses. E. crisbum in the sense of Montagu (1808) and Brown (1827) probably belongs here. Spinose forms of this species were originally recognized as var. aculeatum by Sylvestri (a homonym of Polystomella aculeata d’Orbigny). However, there is little doubt that spines tend to be developed as a juvenile feature and Adams (1963) was able to show that apparently unornamented forms sometimes revealed spinose early chambers in thin section. It a name is thought necessary then spinosum of Atkinson is available. Elphidiwm macellum sensu Heron-Allen & Earland (1909) does not belong here. DISTRIBUTION. This species was first described from ‘Zoophytic Concretions’ in the Mediterranean and Cushman used material from Rimini and Sebenico on the Adriatic and from off the Island of Delos. Other records are: Indian Ocean, beach sand, Karachi (Cushman, 1939); off South Africa (Brady, 1884); South Pacific, off Sydney (Brady, 1884); South Atlantic, Falklands (Brady, 1884; Boltovskoy, 1953, 1954, 1963). This species was also found in the post glacial deposits of Norway by Feyling- Hanssen (1964). Elphidium magellanicum Heron-Allen & Earland (Pl 22, tig. 5; Plozwonigs 50; Pl 26, fe. 11; Ph 28 esis Elphidium (Polystomella) magellanicum Heron-Allen & Earland, 1932 : 440, pl. 16, figs 26-28. Elphidium magellanicum (Heron-Allen & Earland) Cushman, 1939: 62, pl. 17, figs 14, 15 (after Heron-Allen & Earland); Haake, 1962 : 48, pl. 5, fig. 8. Cribrononion magellanicum (Heron-Allen & Earland) Lévy e# al., 1969 : 94, pl. 1, figs 7a, b; pili, ties 35 4, DiaGnosis. A small, compressed species ot E/phidium with lobate to pentagonai periphery and five or six chambers visible. The irregularly developed septal pits are almost hidden by tubercles. DESCRIPTION. (Pl. 24, figs 5, 6; Pl. 26, fig. 11.) Test compressed with wae flat umbilicus on both sides, outline subpentagonal, periphery subrounded; five chambers visible, arranged in an involute planispire, slowly increasing in size and last chamber irregularly subquadrate; irregularly developed septal pits at sutures which curve evenly back to the periphery, pits confined to chamber sides; wall radial, minutely perforate with pores less than I micron in diameter; aperture a series of irregular openings at the basal suture ot the last chamber, hidden by small tubercles which also cover the umbilicus on each side and wide areas each side of the rows of pits. DIMENSIONS. Maximum diameter 0-24 mm, maximum width approx. 0-08 mm. MATERIAL. More than 25 specimens. VARIATION. The chief variation is from specimens with rounded chambers and lobate periphery (Pl. 26, fig. 11) to forms more compressed and pentagonal in CARDIGAN BAY “-RECENT.FORAMINIFERA 203 outline like the specimen described. Two thin sections show specimens with proloculus about 40 microns, presumably megalospheric and 5:5, chambers in two whorls following the proloculus (Pl. 28, fig. 5). Some specimens show six chambers at the periphery. DerositoRY. B.M.(N‘H.) Slide 1970: I1 :26 : 415-418. . Stub 1970: 11 : 20: gma.) Sections 1970-: 11: 26: 502, 1970 : II : 26 : 503. PROVENANCE. Station IV, Clettwr Transect, Dovey Marshes. REMARKS. Our specimens come close to the types and similarly have the sutural depressions covered with ‘snow-like’ granules. The size range also seems to be the same, given as up to 0-35 mm diameter. There is no development of real septal bars and in this character the species comes near ElpMidiella. DISTRIBUTION. This species was first described from the Straits of Magellan and additional records for the South Atlantic are: San Blas Bay (Boltovskoy, 1954); Rio de la Plata (Boltovskoy, 1957) and Puerto Deseado, Patagonia (Bol- tovskoy, 1959). British records include: Western Approaches (Murray, 1970); Plymouth (Murray, 1965); Christchurch (Murray, 1968). Further records off N.W. Europe are given for Germany, Langeoog (Haake, 1962) and France, Dunkirk (Lévy et al., 1969). Elphidium margaritaceum (Cushman) (Pl. 24, figs 12, 13; Pl. 20, fig: 8) | Elphidium advenum (Cushman) var. margaritaceum Cushman, 1930 : 25, pl. Io, fig. 3; 1939 : 61, pint, 1g. 2; Parker, 1952a : 411, pl. 5, fig. 4; 1952b :.447, pl. 3, fig. ro. _ Elphidium margaritaceum (Cushman) Voorthuysen, 1958 : 32, pl. 23, fig. 13; Todd & Low, mgor. ror pl. 2, fig. 3; Haake, 1962 : 49, pl. 5, fig. 11. _ Polystomella macelia Heron-Allen & Earland, 1909 : 696, pl. 21, figs 3a, b (not Fichtel & Moll). Diacnosis. A compressed species of Elphidimwm with acute periphery. About ten chambers visible, slowly increasing in size, raised and densely perforated and _ tuberculate having the appearance of frosted glass. DESCRIPTION. (Pl. 24, figs 12, 13.) Test compressed, almost circular in outline, | ao: periphery acute, shallow umbilicus on both sides; chambers arranged in an involute planispire, nine visible, very slowly increasing in size; irregular septal pits well developed, the rows curved gently back to the periphery, up to eight on each side of the chambers, septal bridges bar-like and covered with tubercles, | covering less than one-third of the chamber surface and depressed below the level _of the rest of the chamber which is evenly raised; wall radial and densely perforated “with pores which reach about I micron in diameter; aperture a row of irregular | openings along the basal suture of the last chamber; small tubercles, about 3 microns in diameter cover most of the surface but are most densely developed in and around | ‘the septal pits and below the apertural face. oe 204 hs eee TEU NOES DimENsIoNS. Maximum diameter 0-41 mm, maximum width approx. 0:15 mm. MaTerRIAL. More than 25 specimens. VARIATION. Specimens have been found up to 0-5 mm in diameter, generally with nine or ten chambers visible. A thin section (Pl. 20, fig. 8) of one specimen reveals: Prolocus diameter Chambers in following whorls Total/visible Test diameter approx. 30 microns S210 B= ; 20) 0-48 mm There is a tendency for an irregular increase in the size of the chambers in some speci- mens and occasionally some of the chambers are smaller than the ones preceding, altering the outline of the test. DEPosITORY. B.M.(N:H.) Stub’ 1970 : 11 > 260 : 602. Section. 1070 = 11) 426m Sor. (Side 197 = 2) 10157. PROVENANCE. Specimen described, CB 335. REMARKS. This species was first described by Cushman as a variety of E, advenum. However, it differs in a number of features from that species. It has fewer chambers, lacks the prominent umbilical bosses and possesses characteristically frosted and raised chamber walls. Elphidium macellum sensu Heron-Allen & Earland probably belongs here and possibly also FE. macellum part of Cushman, 1949 : 27, pl. 5, figs 7a, b (not 8a, b). DISTRIBUTION. The species was first described from beach sand at Rhode Island. Other references for the Western Atlantic include: New Hampshire (Parker, 1952a); Long Island—Buzzard’s Bay area (Parker, 1952b); Martha’s Vineyard, Massachu- setts (Todd & Low, 1961). Records for the North Sea area include: Germany, Langeoog (Haake, 1962). Voorthuysen’s record is from the Eemian of the Netherlands (1958). Elphidium selseyense (Heron-Allen & Earland) sensu lato (Pl. 22,figs 3, 4; Pl. 24, fie. 11; Pl. 26; fies 4,.5,°7, 0, 10; Pl. 20m ies sig) Polystomella striatopunctata (Fichtel & Moll) var. selseyensis Heron-Allen & Earland, 1911 : 448. Type description and figure 1909 : 695, pl. 21, figs 2a-—c. Elphidium selseyense (Heron-Allen & Earland) Cushman, 1939 : 59, pl. 16, figs 26-28 (figures after Heron-Allen & Earland); Parker, 1952b : 449, pl. 4, fig. 9; Voorthuysen, 1958 : 31, pl.'23, fig. ‘9; Haake, 1962 7.40; pl. 5, figs 12-15); pl, figs 1-5. ~ Dracnosis. A compressed species of Elplidiwm with irregular development of septal pits and variable development of granules along the sutures and in the umbilicus. The sutures are often deeply fissured and the periphery entire to lobate. DESCRIPTION. (PI. 22, fig. 4; Pl. 26, fig. 7.) Test compressed, periphery rounded, entire becoming semi-lobate at the last few chambers; chambers arranged in al involute planispire, 11 visible at the exterior, very gradually increasing in size; septal sutures curved back, fissured with irregular development of septal pits, no regular development of septal bridges; wall radial and densely perforated with pores | CARDIGAN BAY RECENT FORAMINIFERA 205 about I micron in diameter; aperture a series of irregular openings along the basal suture of the last chamber; sutural fissures lined with small, irregular granules which also fill the umbilicus and extend along the base of the apertural face, umbilicus also occupied by the irregular lobate ends of the chambers. DimENSIONS. Maximum diameter 0:42 mm, approx. width 0-18 mm, widest at umbilicus. MATERIAL. More than 25 specimens, all growth stages; this species being one of the dominants in Cardigan Bay. VARIATION. Both entire and lobate forms occur with the tendency for the outline to become more lobate with growth. The specimen illustrated (Pl. 22, figs 1, 2; Pl. 26, figs 5, 10) may represent a distinct variety being inflated and lobate from early in growth, with wide depressed umbilicus filled with fine material, markedly fissured sutures, areal apertures and pores up to 3 microns in diameter. Specimens also occur with more marked umbilical bosses (PI. 26, fig. 4) approaching FE. clavatum but lacking the single, elevated, umbilical boss diagnostic of that species as emended by Loeblich and Tappan. In Pl. 22, fig. 3; Pl. 26, fig. 9 we illustrate a specimen with irregular almost bulla-like final chamber bearing areal apertures with protruding necks and large pores up to 2 microns in diameter. Some specimens show small, round bosses in the umbilical area and extending along the sutures; these approach E. lidoense Cushman. Specimens develop up to three whorls, generally with 9-11 chambers visible on the exterior. Two thin sections (Pl. 29, figs 1, 2) show the following: visible total diameter chambers per whorl externally — proloculus diameter entire specimen 0-40 mm 7:8:2—, fe) 35 microns lobate specimen 0-43 mm 7:8: 3—, ) 35 microns The rate of chamber size increase in both cases is: to end of first whorl x2, to end of second whorl x1. weeosirory. B.M.(N.H.) Slides 1970 :'11 : 26: 419, 420, 1970 : 11 726: 421- Weegee 1070: 11 : 26: 424, 425 (lobate var.).. Stub 1970 : Ir : 26.:.599-601, 605, Gig Sections 1970 : II : 26 :°504, 1970 : II :.26.: 505. PROVENANCE. Described specimen, CB 62. Other specimens illustrated, CB 58. _ Lobate variety, Clettwr Transect, Dovey Marshes. REMARKS. Our specimens closely resemble material placed by Heron-Allen and Earland in the ‘Students Collection’ in the British Museum and also material picked from Selsey shore sand which includes both entire and lobate specimens with both raised and sunken umbilical areas. What Heron-Allen and Earland veferred to in their description as a vesicular extension of the final whorl into the umbilicus proves to be fine grained, granular calcite. The type figures show one >pecimen with nine chambers visible and one, more lobate, with 11 visible. _ A similar range of form to that in our specimens was noted by Haake (1962) in material from N. Germany. 206 Js (Re =e AaYINTSS Lutze (1965) followed by Lévy et al. (1969) supposed E. selseyense to be a junior synonym of E. excavatum (Terquem) described from the shore sands of Dunkirk (1875). However, Terquem’s type figure apparently shows a non-granulate form with excavated umbilicus. The specimen is lost but Lévy e al. in their redescription of a topotype state that the umbilicus is without granules; this diagnosis excludes E. selseyense. On the other hand, intermediate forms which they describe between E. excavatum and E. lidoense presumably are E. selseyense. As noted some of our specimens show the areal apertures of ‘Cribroelbhidium’ DISTRIBUTION. This species was first described from the shore sands at Selsey Bill in the English Channel and is recorded by Murray from Plymouth (1965a) and from the Western Approaches (1970) and by Atkinson (1970) from the Scillies. Other records for N.W. Europe are: N. Germany, Langeoog (Haake, 1962); N. France, Dunkirk (? part E. excavatum Lévy et al., 1969). | There is one record for the Western Atlantic (Parker, 1952b), other records may be included under L’. incertum and FE. clavatum. Elphidium waddenstis (Voorthuysen) (Pl 24) fies 410 Pl 26, fier 1; Rl 28, tesrOnstsn) Elphidium guntert Cole var. waddensis Voorthuysen, 1951 : 25, pl. 2, figs 16a, b. Elphidium guntert Tood & Low, 1961 : 19, pl. 2, fig. 10; Haake, 1962 : 48, pl. 5, figs 3, 4 (not =. gunteri Cole). Driacnosis. A coarsely perforate Elphidium with up to 14 rather narrow, de- pressed chambers and irregularly developed septal pits (fossettes). DESCRIPTION. (Pl. 24, figs 4, 10.) Test semi-inflated with irregular outline, periphery rounded, semi-lobate; ten chambers visible arranged in a planispire, increasing slowly in size, depressed; irregular development of square septal pits or fossettes at the sutures which in some cases appear simply irregularly incised, about four pits on each side, where developed, extending to the periphery, septal bars short; wall radial and coarsely perforate with both very fine and large pores up to 3 microns in diameter; aperture a series of irregular openings at the basal suture of the last chamber; apertural face only finely perforate with round tubercles at the base; rounded glassy beads in the umbilicus as well as tubercles which extend along the sutures and are particularly well developed below the apertural face. Dimensions. Maximum diameter 0-29 mm, maximum width approx. o-II mm, MATERIAL. More than 25 specimens, most of them small, generally golden-brown in colour. VARIATION. The chambers gradually increase in size and number per whorl. Externally visible chamber number varies from about nine in the smaller specimens to 14 in the largest noted, 0:35 mm in diameter. The chambers tend to become narrow and in some cases appear pressed back on each other giving an irregular | outline. A thin section (Pl. 28, fig. 10) shows a large proloculus of approx. 70 microns diameter with 7 : 12 : 4—, chambers in the following whorls, 24 chambers in all. — a CARDIGAN BAY RECENT FORAMINIFERA 207 Derosirory. B.M.(N:H.) Slide -1970 : 11-: 26-: 436-430. Section 3I970.:1L: Se o00,) Stubs,1970 : Ir: 20: 598, 1970.2, 11 + 26.:.758. PROVENANCE. Specimen described, Clettwr Transect, Station II, Dovey Marshes. Remarks. This species was originally described as a variety of EF. gunteri Cole known from the Pliocene of Florida. However, that species differs in being larger with much more regularly developed sutural pits and bars, up to Io on each chamber side, it is also smoother. The specimens referred by Todd and Low and by Haake to Cole’s species also appear to belong here. Our specimens are identical with topotypes of Voorthuysen’s variety on file at the British Museum. Dr John Murray (personal communication) has referred specimens similar to ours to E. oceanensis (d’Orbigny). However, the type figures given by Fornasini (1904) appear to show high rather than depressed chambers and a smooth periphery ; other details are not made clear. DISTRIBUTION. This species was described from the Holocene and Recent in the Wadden See off Groningen, Netherlands. Other records for N.W. Europe are: Germany, Langeoog (Haake, 1962); France, Dunkirk (Lévy e¢ al., 1969). It is also described from the marshes of Martha’s Vineyard, Massachusetts (Todd & Low, 1961). This resembles its distribution on the Dovey Marshes where it is a frequent living form, usually golden-brown in colour. Elphidium williamsoni Haynes n. sp. (eliz24, fie.°7; Pl. 25, figs 6,-9; Pl. 27, figs 1=3) Polystomella umbilicatula Williamson, 1858 : 42, pl. 3, figs 81, 82; Terquem, 1875 : 429, pl. 2 figs 3a, b (not Nautilus umbilicatulus Walker & Jacob). _ Elphidium umbilicatulum (Williamson) Lévy et al., 1969 : 96, pl. 1, figs 6a, b; pl. 2, figs 1, 2. Elphidium excavatum Cushman, 1930 (part) : 21, pl. 8, figs 4-7 only; 1939 : 58, pl. 16, figs 10-12 olive 1949 : 28; pl.-6, figs 2a, b; Todd & Low, 1961 : 19, pl. 2, fig. 5; Haake, 1962 : 47, pl. 5, fig. 5; Feyling-Hanssen, 1964 : 344, pl. 20, figs 7, 8; Brodniewicz, 1965 : 214, pl. 8, fig. 5; pie, fis. 4; Adams-& Frampton, 1965 : 58, pl. 5, fig. 7; Murray, 1965a : 503 (list) “pl. 1, _ fig. 6, 6 (stereopairs) (not Terquem). Cribrononion cf. alvarezianum Lutze, 1965 : tot, pl. 15, fig. 46 (not Polystomella alvareziana d’Orbigny). _ Diacnosis. A rotund species of Elphidium with rounded periphery and slight, _ father flat umbilicus on each side filled with the irregular ends of the chambers. Fossettes and septal bars well developed, reaching about eight or nine in number om each side and covering about half the chambers. Up to 14 chambers visible. Wall smooth with relatively sparse tubercles within the septal pits and at the base pf the apertural face. | Description. (Holotype, Pl. 24, fig. 7; Pl. 25, figs 6, 9.) Test semi-inflated, lightly umbilicate with rounded periphery, entire becoming semi-lobate at the last ew chambers—chambers arranged in an involute planispire, 13 visible, slowly ‘creasing in size with marked septal pits (fossettes) increasing from six to eight or tine on each side (ten on third chamber from the last), strong, narrow septal bars | } | t 208 J. R. HAYNES alinost equal in length to the rest of each chamber, in one case (on the last chamber) with a proximal opening, pits lozenge-shaped, tuberculate within; septal sutures flush—not visible; wall radial, finely perforate, pores rather less than I micron in diameter, tuberculate below the apertural face ; aperture a series of irregular openings along the basal suture of the last chamber, linking with the pits of the first exposed chamber. Dimensions. Diameter 0-48 mm, width approx. 0-20 mm. MATERIAL. More than 25 specimens. Very abundant in the marshes. VARIATION. There is some variation in the degree of inflation and some specimens are slightly more subangular at the periphery. Variation of chamber number as seen externally is largely a function of growth, there being a gradual increase with each whorl. Thin sections show megalosphere sizes near 50 microns and the speci- men illustrated (Pl. 27, fig. 1) has 7 : 9 : 7—, chambers in each whorl following the proloculus, with 11 visible at the periphery. : DeposiTorY. B.M.(N.H.) Slide 1970 : 11 : 26 : 431, 432 (paratypes). Sections 1970 : II : 20: 507, 19070 : 11 : 20 : 508 (paratypes): Stub “10707 11 20uaea (holotype). PROVENANCE. Described specimen and specimens cut Clettwr Transect, Station II, Dovey Marshes. REMARKS. This species was for a long while confused with EF. excavatum Terquem. After study of topotype material, Lévy et al. have reverted to Terquem’s original conception of that species and include E. selseyense within its limits. The inflated, many chambered, marsh and estuarine form widely referred by authors to E. excavatum is referred by them to E. umbilicatulwm = Polystomella umbilicatula (Wiliamson) not Nonion umbilicatulum (Walker & Jacob). However, this contra- venes article 49 of the International Committee on Zoological Nomenclature as Williamson clearly put his species in synonymy with that of Walker and Jacob. This species is therefore renamed E. williamsont. Cribrononion cf. alvarezianum ot Lutze also belongs here. See also under E. selseyense. When living this species is usually found coloured green with contained algae. DISTRIBUTION. This species is widespread around the British Isles (often erroneously recorded previously as Polystomella striato-punctata (Fichtel & Moll) particularly in the estuarine environment. Williamson mentions specimens ob- tained from the stomach of a shell drake shot in Belfast Bay, unmixed with any other foraminifera. He supposed this ‘bonne bouche’ to have been selected via an inter- mediate predator such as a mollusc but in fact this species can sometimes occur to the exclusion of other forms in the Dovey Estuary, also the haunt of shell duck. Other records for N.W. Europe are: N. France, Dunkirk (Terquem, 1875; Lévy et al., 1969); Belgium (Cushman, 1949); Germany, Langeoog (Haake, 1962); Ostsee (Lutze, 1965); Poland. Baltic (Brodniewicz, 1965); Holocene of Oslofjord (Feyling- Hanssen, 1964). Records from the Western Atlantic include: Massachusetts, Martha’s Vineyard (Todd & Low, 1961). | CARDIGAN BAY RECENT FORAMINIFERA 209 Confusion of this species with both E. excavatum and E. selseyense makes other records, especially those from farther afield doubtful. Genus NONION Montfort, 1808 Nonion depressulus (Walker & Jacob) (Pl. 22, figs 8-11; Pl. 29, fig. 9; Text-fig. 44, nos 1-3) ‘Nautilus spiralis utrinque subumbilicatus’ Walker & Boys, 1784 : 109, pl. 3, fig. 68. Nautilus depressulus Walker & Jacob, 1798 : 641, pl. 14, fig. 33. Nonion depressulum (Walker & Jacob) Cushman, 1930 : 3, pl. 1, fig. 3 only; Murray, 1965b : 148, pl. 25, figs 6, 7; pl. 26, figs 7, 8 (as depressulus). Nonion asterizans Heron-Allen & Earland, 1913b : 143, pl. 13, figs 12, 13; Le Calvez, 1958 : 168, mlx, fg. 13 (not Fichtel & Moll). Dracnosis. A compressed species of Nonion with between 8 and 14 chambers visible at the periphery, but generally nine or ten. Chambers rather high and tend- ing to uncoil slightly from the umbilicus which is filled with granules of calcite _ and an off centre, glassy boss (both sides). Sutures often hooked back towards the umbilicus, excavated with the granular umbilical material extending along them producing a star shape. Periphery subrounded. DESCRIPTION. (Pl. 22, figs Io, 11.) Test compressed with flattened sides, slightly uncoiled, bi-umbilicate, periphery subrounded becoming semilobate at the _last few chambers; chambers arranged in a planispire, gradually increasing in size and becoming much higher than long, ten visible at the periphery with slight, umbilical lobes; sutures slightly curved back and almost radial towards the periphery, hooked back at the umbilicus, strongly incised; large umbilicus on either side with glassy boss and with granules of calcite which extend along the sutures; wall granular, finely perforate; aperture a row of small irregular holes between rough granules at the basal suture. DimENsIonsS. Maximum diameter 0-24 mm, thickness 0-7 mm. _ Matertar, More than 25 specimens, mostly small. | VARIATION. Specimens up to 0-40 mm, maximum diameter occur and show from 8 to 11 chambers at the periphery (Text-fig. nos 1-3). This variation is prob- ably related to proloculus size. S @eerecitory. B.M.(N.H.) Slide 1970 : 11: 26: 443, 444.°Section 1970: 11: 26 #509. Stub 1970 : 11 :.26 : 658, 063, 664. | PROVENANCE. Specimen described, CB 463. Other specimens figured, nos I, 2, vB 13, no. 3, CB 54. Specimens illustrated Pl. 22, figs 8-11, Station VII, Clettwr ransect, Dovey Marshes; specimens thin-sectioned from the same locality. | Remarks. Dr F, T. Banner has pointed out to us that although Dr John Murray ‘mended the diagnosis of this species on the basis of topotypes from Reculver each sands he did not erect a neotype. To avoid further confusion we now ‘ropose that his topotype, Reg. no. 1962.2.12.533, becomes the neoholotype. i This species has been widely confused with the common marsh form now referred 210 J. R. HAYNES tc Protelphidium anglicum and in marine waters has masqueraded under the name of its relative, N. asterizans, a larger form with angular periphery and higher chambers. DISTRIBUTION. This species was described from the shore sands of Reculver, East Kent and has been recorded also from the West of Ireland, Clare Island (Heron- Allen & Earland, 1913b) and the Celtic Sea (Le Calvez, 1958). It is recorded by Murray from the Tamar Estuary (1965a), from Christchurch Harbour (1968) and from the Western Approaches (1970). Nonion (Florilus) pauperatum (Balkwill & Wright) (Pl. 22, figs 13, 14; Pl. 23, fig. 4; Text-fig. 44, nos 4-7) Nonionina pauperata Balkwill & Wright, 1885 : 353, pl. 13, figs 25, 26; Halkyard, 1889 : 71, pl. 2, fig. 13; Heron-Allen & Earland; 1o11 : 342, pl. 11, figs 16, 17. Nonion pauperatum (Balkwill & Wright) Cushman, 1930 : 13, pl. 5, figs 4, 5, 7 (after Balkwill & Wright, Halkyard and Heron-Allen & Earland); 1949 : 26, pl. 5, fig. 5; Haake, 1962 : 42, pl 3; les 6; 7- Diacnosis. An angular species of Nonion (Florilus) with eight or nine chambers visible and distinct, limbate sutures meeting in a large, flat boss (on each side). DESCRIPTION. (PI. 22, figs 13, 14.) Test compressed, tapering from the umbilici to the angular periphery, semi-lobate; chambers arranged in an involute planispire, slowly increasing In size as added, becoming much higher than long, triangular in apertural view, nine visible at the periphery; sutures distinct, limbate, swept back, 3 0.0 0.5mm. Fic. 44. 1-3. Nonion depressulus. 1, side view of eight chambered specimen, probably megalospheric; 2, apertural view; 3, side view of specimen with 11 chambers visible. 4-7. Nonion pauperatum. 4, apertural view of specimen with eight chambers visible externally; 5, side view; 6, apertural view of specimen with nine chambers visible; 7, side view. CARDIGAN BAY RECENT FORAMINIFERA 211 meeting in a flat, glassy boss; wall granular, distinctly perforated with pores about 4 micron in size; aperture comprising two elongate, areal slits near the basal suture, one on each side, overlapping at the periphery; granules of calcite developed below the apertural face. DIMENSIONS. Maximum diameter 0-30 mm, thickness 0-12 mm. MATERIAL. Six specimens. VARIATION. The specimens which apart from the one described are all less than 0:30 mm in diameter show irregular lobation of the outline (Text-fig. 44). The aperture is a variable basal to raised oblong opening at the periphery (areal when examined in detail). Deposirory. B.M.(N.H.) Slide 1970 : 11 : 26: 445-449. Stub 1970: 11: 26: 661. | PROVENANCE. Specimen described, CB 477. Other specimens illustrated figs 6, 7, CB 501, figs 4, 5, CB 542. REMARKS. Viewed with the light microscope this small species appears to have a basal aperture extending up into the apertural face as an oblong arch. Before the details revealed by the stereoscanner photo are seized on as being of generic _ significance more work must be done on allied Nonion (Florilus) species; many of _ which have similar arched apertures. DISTRIBUTION. This species was first described from the Irish Sea and there are a number of records from west of the British Isles: Dublin coast (Balkwill & Wright, 1885); Southport, Lancs. (Chaster, 1892); West of Ireland, Dogs Bay (Wright, 1900); Clare Island (Heron-Allen & Earland, 1913b); West of Scotland (Heron-Allen & Earland, 1916a); English Channel, Selsey (Heron-Allen & Earland, 1911); Jersey -(Halkyard, 1880). _ It has been recorded from N. Germany, Langeoog by Haake (1962) and there is also an Eemian record for the Netherlands (Voorthuysen, 1958). Genus NONIONELLA Cushman, 1926 Nonionella auricula Heron-Allen & Earland (Text-fig. 45, nos I-3) ’onionella auricula Heron-Allen & Earland, 1930 : 192, pl. 5, figs 68-70; Cushman, 1939 : 33, | pl. 9, figs 7-9 (after Heron-Allen & Earland) ; Voorthuysen, 1960 : 254, pl. 11, fig. 22; Feyling- | anssen, 1964 : 327, pl: 16 figs 21~23. Diacnosis. A minute, glassy, subglobose species of Nonionella with chambers ecoming about twice as high as long. Last chambers not projecting much into the central umbilicus which is small and deep. | Description. Test compressed, subglobose, ear-shaped with semi-lobate, unded periphery ; 11 chambers following the proloculus, arranged in a low, sinistral oH | 212 J. R. HAYNES trochospire, 8 : 3—, gradually increasing in size as added, inflated, becoming twice as high as long, last one slightly projecting into the ventral umbilicus; sutures dis- tinct, impressed, radial on the ventral side, slightly curved back on the dorsal side; | wall translucent, distinctly perforate; aperture apparently ventral and basal; — distinct ventral umbilicus. | DimENSIONS. Maximum diameter 0:15 mm, width 0:10 mm, thickness 0-66 mm, proloculus diameter approx. 15 microns. MATERIAL. One specimen only. Depository. B.M.(N.H.) Slide 1970 : 11 : 26: 450. PROVENANCE. Aberystwyth Harbour. REMARKS. Our specimen is very close to the types in general morphology and in size. Heron-Allen and Earland give a range of 0:18-0:25 mm for the maximum | diameter with up to 13 chambers developed. The specimens described by Voort- | huysen and Feyling-Hanssen also come very close but specimens ascribed to this species from the Arctic (Loeblich & Tappan, 1953) and from off the N.E. seaboard of the United States, New England (Cushman, 1944; Parker, 1952a) are much larger and more compressed with entire periphery and higher chambers (see especially fig. g of Loeblich & Tappan). These last appear to be closer to the specimens we describe below as Nonionella species A. DISTRIBUTION. This tiny, vitreous species was first described from the English — Channel near Plymouth. It has also been found living off the N. Kent coast, Hedley & Underwood (1957) and is listed from the Scillies by Atkinson (1970). It has also been recorded from the Dollart-Ems Estuary (Voorthuysen, 1960) and from the Holocene of Oslofjord (Feyling-Hanssen, 1964). O90 0.0 0.5mm. | | Fic. 45. 1-3. Nonionella auricula, specimen described. 1, dorsal view; 2, side view; | 3, ventral view. 4. Nonionella turgida, specimen with large umbilical process. 5, ©. | Nonionella turgida var. digitata. 5, ventral view; 6, dorsal view, specimen broken. | CARDIGAN BAY. RECENT -FORAMINIFERA 213 Nenionella turgida (Williamson) (Pl. 22, fig. 12; Text-fig. 45, no. 4) Rotalina turgida Williamson 1858 : 50, pl. 4, figs 95-97. Nonionina asterizans var. turgida (Williamson) Carpenter, Parker & Jones, 1862 : 3IT. Polystomella crispa sp., var. (Nonionina) turgida (Williamson) Parker & Jones, 1865 : 405, pl. 17, figs 57a-c. Nonionina turgida (Williamson) Brady, 1884 : 731, pl. 109, figs 17-19; Goés, 1894 : 105, pl. 17, fe. 632. ee conella turgida (Williamson) Cushman, 1930: 15, pl. 6, figs 1-4, 1 after Williamson and 2 after Brady; 1939 : 32, pl. 9, figs 2, 3; Feyling-Hanssen, 1964 : 328, pl. 17, figs 2-6. Diacnosis. (Pl. 22, fig. 12.) A compressed species of Nontonella with chambers increasing very rapidly in height and the final one extending in a broad lobe across the ventral umbilicus. | DESCRIPTION. Test compressed, ovate in outline with pointed apex, periphery rounded, entire; about 11 chambers in a low, sinistral trochospire, increasing rapidly in height, subglobose, last one extending in a broad lobe across the ventral umbilicus, nine visible on ventral side; sutures distinct, incised, radial; wall apparently granular, thin, densely but minutely perforate; aperture ventral and basal with a lip extending from the periphery into the umbilicus. Dimensions. Length 0-21 mm, width 0:13 mm, thickness about 0-Io mm, MATERIAL. Three specimens. VaRIATION. As shown in Text-fig. 4 and by authors’ figures there is considerable variation in the strength of development of the umbilical lobe. Darostory. B.M-(N.H:) Slide 1970 : 11 : 26:.451. Stub 1970 :.11 : 26 : 666. PROVENANCE. Specimen described and illustrated by Stereoscanner photo, CB 562. Other specimen illustrated, CB 382. REMARKS. Williamson’s type figure clearly shows an inequilateral test with the last chamber developing an umbilical bulge on the ventral side. Our specimens although smaller and less developed show essentially the same features. Some difficulty has been introduced because Brady (fig. 17, 1884) included in his concept of the species an aequilateral specimen from the Porcupine Station 67, East of the Shetlands. This has been accepted by later workers possibly partly because the igure was copied and wrongly ascribed to Williamson by Cushman (1930) on his _ dlate explanation, though not in the text. However, Cushman also figured another similar, specimen from S.W. of Ireland. These probably do not belong here. | DistRIBUTION. This species was originally described as common off the Shetlands and Arran, West of Scotland and also rare at Whitehaven, Cumberland, N. Irish vea. Subsequent records confirm this concentration off western coasts of the 3ritish Isles: Irish Sea (Balkwill & Wright, 1885); Dee (Siddall, 1876); Southport ieee. 1892) ; West of Scotland, Shetlands (Waller, 1868) ; Faroe Channel (Pearcey, 890); Inner Hebrides (Heron-Allen & Earland, 1914a, 1916a; Robertson, 1892) ; lyde (Robertson, 1877); West of Ireland (Wright, 1889); Dogs Bay (Wright, 1900) ; 214 J. R. HAYNES Clare Island (Heron-Allen & Earland, 1913b); English Channel, Eddystone (Robert- son, 1870); Cornwall (Heron-Allen & Earland, 1916b); Plymouth (Heron-Allen & Earland, 1930;) Celtic Sea (Le Calvez, 1958); Western Approaches (Murray, 1970) ; North Sea, off Durham (Robertson & Brady, 1870); Forth (Pearcey, 1902). Other N.W. European records are: Scandinavia (Goés, 1894; Kiaer, 1900); Holocene, Oslofjord (Feyling-Hanssen, 1964); Hardangerfjord (Holterdahl, 1965). North Atlantic records are: Bay of Biscay (Berthois & Le Calvez, 1959); E. Atlantic (Brady, 1884); West Atlantic (Parker, 1948); Arctic (Cushman, 1948; Parker & Jones, 1865); Iceland (Norvang, 1945). Caribbean records include: Gulf of Paria (Todd & Bronniman, 1957). South Atlantic: Falklands (Farland, 1934); off Brazil (Boltovskoy, 1959); off Argentina (Boltovskoy, 1961; Brady, 1884). Mediterranean: Western (Todd, 1958); Tyrrhenian Sea (Norin, 1958); Eastern (Parker, 1958); Gulf of Naples (Hofker, 1960); Adriatic (Cita & Chierici, 1962); off Israel (Reiss, Klug & Merling, 1961). . ? Pacific: off California (Natland, 1933); off Japan (Brady, 1884); eight stations in the S. Pacific including off New Zealand (Brady, 1884); Malay Archaepelago (Millett, 1898); Manukau Harbour, New Zealand (Hulme, 1964). These records suggest in general a cool temperate distribution. Nonionella turgida (Williamson) var. digitata Norvang (Text-fig. 45, nos 5 and 6) Nonionella turgida var. digitata Norvang, 1945 : 29, text-fig. 4; Cushman, 1948 : 55, pl. 6, fig. 5 (after Norvang); Parker, 1952a : 413, pl. 5, figs 15, 16. DiaGnosis. A variety of Nonionella turgida with digitate margin to the umbilical process. DESCRIPTION. Test with last chamber broken and others holed, elongate-ovate with pointed apex, subglobose, periphery rounded; nine chambers following the proloculus in a low, dextral trochospire, becoming high but less than twice as high as long, gradually increasing in size as added, inflated, seven visible on the involute ventral side; sutures incised, radial on the ventral side, swept back on the dorsal side; wall apparently granular, thin, transparent, finely and densely perforated; last chamber extending over the ventral umbilicus with digitate margin, the finger- like processes extending along the line of the sutures. DIMENSIONS. Maximum length 0-17 mm, width o-10 mm. MATERIAL. One specimen only. DEposiIToRY. B.M.(N.H.) Slide 1970 : 11 : 26: 452. PROVENANCE. CB 646. REMARKS. Our specimen appears to show the incipient development of the remarkable ‘tubulose appendices’ which in the type partially cover the earlier cham- CARDIGAN BAY RECENT FORAMINIFERA 215 bers. A similar development occurs in Elphtdium selseyense (Pl. 22, fig. 3) and is probably connected with a particular phase of ontogeny. It is reminiscent of the bulla in certain Globigerinidae. DISTRIBUTION. This variety was described from Pistilfj6rour, Iceland and has also been recorded from off the N.E. seaboard of N. America, Portsmouth, New Hampshire (Parker, 1952a). Nonionella (? Nonionellina) species A (Pl. 22, figs 17, 18; Pl. 23, fig. 3; Text-fig. 46, nos 1-4) DiaGnosis. A compressed species of Nonionella with chambers becoming more than three times as high as long; test apparently tending to become almost planispiral and aequilateral in the last part; ventral umbilicus tuberculate. DESCRIPTION. (PI. 22, figs 17, 18; Pl. 23, fig. 3.) Test compressed, ear-shaped with entire to slightly lobate, subround periphery; chambers arranged in a low, dextral trochospire, ten visible at the periphery with flattened sides, gradually _ Increasing in size as added, last one more than three times as high as wide and projecting into the ventral umbilicus; sutures thickened and incised, swept back; wall thin, apparently granular, finely and densely perforate; aperture a series of small irregular openings at the ventral, basal suture of the last chamber surrounded by tubercles which fill the umbilicus and line the sutures. DIMENSIONS. Maximum diameter approx. 0:50 mm, width 0-35 mm, thickness 0-15 mm. MATERIAL. Four specimens. | 0.0 0.3mm. _ Fic. 46, 1-4. Nonionella species A. 1-3, specimen showing almost equal involution on both sides; 1, view of ventral side; 2, edge; 3, dorsal side; 4, additional specimen, side view. 216 J. R. HAYNES VARIATION. The text figures show two of the other specimens recovered, both are broken but the more complete one, nos 1-3, shows the tendency for both sides to become involute and the test almost aequilateral with 11 chambers visible. The other specimen shows 12 chambers. Depository. B.M.(N.H.) Slide 1970 : 11 ::26 : 453, 454. Stub 1970 : 112 26% 665. PROVENANCE. Specimen described and illustrated by stereoscanner photos, CB 15. Other specimens, Text-fig. nos 1-3, CB-384; Text-fig. no. 4, CB 343. REMARKS. This species has some resemblance to Nomionella atlantica Cushman but is more compressed and becomes more involute on the dorsal side. Some of the specimens referred to N. auricula from the Arctic and Western Atlantic may be the same (see for instance Loeblich & Tappan, 1953, fig. 9). Nontonella sp. A of Todd & Bronniman (1957) from the Gulf of Paria, Trinidad is also very close. Genus PROTELPHIDIUM Haynes, 1956 Protelphidium anglicum Murray (Pl. 22; figs 15, 167.Pl. 23) figs 1, 2; Pl 27, figs 6-6) Protelphidium anglicum Murray, 1965b : 149, pl. 25, figs 1-5, pl. 26, figs 1-6; 1968 : 94 (list), pl. 1, figs 11a; b: Nonionina crassula Williamson, 1858 : 33, pl. 3, figs 70, 71, as N. umbilicatula on figure (not Walker & Jacob). Nonionina depressula Brady, 1867 : 106 (not Nautilus depressulus Walker & Jacob). Nonion depressulus Cushman, 1930 : 3, pl. 1, figs 3-6; Voorthuysen, 1958 : 28, pl. 23, fig. 2; Haake, 1962 : 40, pl. 3, figs 1, 2 (as depressulum). Protelphidium depressulum Adams & Haynes, 1965 : 36 (list). Diacnosis. An inflated species of Protelbiidium with apertural face not much higher than wide, entire periphery and eight or nine chambers visible externally. Sutures deeply excavated towards the umbilicus and lined with minute tubercles. Wall very thin and minutely perforate. DESCRIPTION. (Pl. 22, figs 15, 16; Pl: 23, figs 1, 2.) Test moderately come pressed with rounded periphery, circular in outline, becoming slightly uncoiled in the last part with small, deep, open umbilicus, periphery entire; chambers arranged in an involute planispire, eight visible externally, gradually increasing in size as added; sutures gently curved back towards the periphery, deeply excavated towards the umbilicus, lined with minute tubercles, approx. 5 microns in length; wall thin, radial, densely and minutely perforated with pores less than I micron in diameter; aperture multiple, apparently a series of small openings along the basal suture of the last chamber, largely hidden by tubercles. DIMENSIONS. Maximum diameter 0-36 mm, width 0-14 mm. MATERIAL. More than 25 specimens. One of the most abundant species in the Dovey Estuary. CARDIGAN BAY RECENT FORAMINIFERA 217 VARIATION. Specimens with nine or even ten chambers visible at the periphery occur and also specimens with the last chambers becoming lobate. Thin sections show that at least two proloculus sizes occur, Pl. 27, figs 6, 9, with chambers developed as follows: Chamber number in Total number Total Proloculus diameter following whorls + proloculus visible Test diameter approx. IO microns 7:9:10:2— 29 9 0-45 mm approx. 40 microns 6:8:5— 20 8 0-35 mm Thus both microspheric and megalospheric forms appear to be present. DeposiTorY. B.M.(N.H.) Slide 1970 : 11 : 26 : 455-462. Sections 1970: 11: mee rO, 1070 : TI: 26 : 511, 1970: 11: 26: 512. Stub 1970: 11 : 26 : 659. PROVENANCE. Specimen described and specimens cut Station III, Clettwr Transect, Dovey Marshes. REMARKS. As shown by Murray (1965b) this brackish water species has been confused with Nonion depressulus. It is distinguished from the neotype of that species by its radial wall structure, inflated, more depressed chambers and open umbilicus also by generally having eight or nine rather than Io or 11 chambers visible externally. . Most references in the British literature to N. depressulus from brackish water habitats probably belong here, such as Brady (1867) who gives a record for the mouth of the Wansbeck on the N.E. coast. A figured reference which can be included with fair certainty in synonymy is Williamson’s of N. crassula. The specimen figured by Brady (1884) from off Sydney, Australia, probably does not belong here. DISTRIBUTION. The types are from Christchurch Harbour, Hampshire. Prob- ably ubiquitous in brackish water habitats around the British Isles. Family UNCERTAIN Genus EPIS TOMINELLA Husezima & Maruhasi, 1944 Epistominella naraensis (Kuwano) | (Pl. 20, fig. 14; Pl. 23, figs 7, 8; Test-fig. 47, nos I-5) _ Pseudoparrella naraensis Kuwano, 1950 : 317, text-figs 6a-c. ? Epistominella sandiegoensis Uchio, 1960 : 68, pl. 9, figs 6, 7. | Pulvinulinella exigua Hofker, 1951a : 322, text-figs 219-221 (not Brady). _ Diacnosis. A small, biconvex species of Epistominella with rounded periphery ind six chambers in each whorl. | DESCRIPTION, (Text-fig. nos 1-4.) Test small, biconvex with rounded periphery ind shallow ventral umbilicus, entire to slightly lobate; 18 chambers arranged in 218 J. R. HAYNES a low, sinistral, trochospire, all visible on the dorsal side, 6 : 6 : 6, in each whorl following the proloculus, gradually increasing in size and becoming longer than high in the second whorl, six visible on the ventral side, umbilical extremities slightly overlapping; sutures slightly impressed, markedly backwards curving on the dorsal side, radial to slightly curved on the ventral side; wall thin, glassy, radial with fine perforations less than } micron in size, ventral umbilical area adjacent to internal tooth plates imperforate; aperture a curved slit almost parallel to the periphery, extending from the basal suture of the final chamber, curving slightly dorsally within a depression in the truncate, apetural face, with denticulate border, the proxi- mal edge passing into a trough shaped internal tooth plate. DIMENSIONS. Maximum diameter 0-13 mm, height 0-o7 mm. Approx. diameter of the proloculus 7 microns. MATERIAL. Six specimens only. VARIATION. Some specimens are rather more lobate and in some cases the final chamber is more subangular at the periphery with subquadrate apertural face (Text-fig. no. 5). In our specimens the proloculus diameter varies between 6- 8 microns, with up to Ig chambers developed, they thus come near to what Hofker described as the B form (microspheric generation) with proloculus of 6 microns dia- meter and up to 17 chambers developed. 0.0 0.2mm. 0.0 O . 1mm. Fic. 47, 1-5. Epistominella naraensis. 1, ventral view; 2, side view; 3, dorsal view; 4, oblique side view of specimen described. N.B. Internal chamber walls seen through the thin glassy outer wall give appearance of double septa; 5, specimen with more angular periphery at last chamber, drawn from stereoscanner photo. CARDIGAN BAY RECENT FORAMINIFERA 219 DerestroRyY. B.M.(N.H.) Slide 1970: 11 :.26 : 463, 464. ‘Stub-1970 ! 11: 26: 610-612. . PROVENANCE. Specimen described, CB 419. Other specimens shown in text-fig. and by stereoscanner photos, Clettwr Transect, Dovey Marshes. REMARKS. Our specimens closely resemble FE. naraensis in chamber number and size, with diameters generally less than 0-2 mm. Epistominella sandiegoensis may be synonymous, as the dorsal and ventral views given are identical with E. naraensis and it is described as biconvex, although no side view is given. EF. vitrea differs in being slightly larger with flattened ventral side. The specimens described as Pulvinulinella exigua by Hofker also appear to belong here as the figures show identical chambering, distribution of pores and aperture shape; Epistominella exigua (Brady) has an acute periphery and must be ruled out. DISTRIBUTION. The types are from the Plocene of Honshu Island, Japan while Uchio’s specimens are from 350 fathoms off San Diego, California. Hofker’s material is also from the Indo-Pacific region and on the equator, though at great depth, 582 fathoms, bottom temperature 6-6°C. It is also recorded by Matoba (1970) from Matsushima Bay, N.E. Japan. Vil. *SUMMARY-AND CONCLUSIONS I. One hundred and sixy-five species are described belonging to 65 genera and 27 families. One genus is new, Eggerelloides, genoholotype EF. scabrum (Williamson) and also the following 12 species: Ammobaculites balkwilli Ammonia aberdoveyensis Buliminella borealis Elphidium exoticum Elphidium williamsonti Guttulina harrist Lagena doveyensis Lagena hibernica Lagena sulcata var. torquiformis Oolina heronalleni Siphonina georgiana — Spiropthalmidium acutimargo var. emaciatum Techmitella teivyense In addition a neotype has been selected and described for Quinqueloculina bicornis (Walker & Jacob) and a neotype for Nonion depressulus (Walker & Jacob) cited from the Murray Collection in the British Museum. 2. Revised identifications of species mentioned in our published lists, apart from simple generic shifts, are as follows: 220 ql. RS PE AWaNGES Ammobaculites agglutinans = A. balkwilli n. sp. Ammonia beccarii batavus (estuary variety) = A. aberdoveyensis n. sp. Buliminella elegantissima = B. borealis n. sp. Cyclogyra involvens = C. selseyensis (Heron-Allen & Farland) | Discorbis baccata = Discorbis wright (Brady) Elphidium crispum = E. macellum (Fichtel & Moll) Elphidium discordale = FE. exoicum nn. sp. Elphidium excavatum = E. williamsoni n. sp. Elphidium granosum = E. waddensts (Voorthuysen) Elphidium voorthuysem = E. incertum (Williamson) Epistominella vitrea = FE. naraensis (Kuwano) Fissurina orbignyana = F, elliptica (Cushman) Nonion asterizans = Nonion depressulus (Walker & Jacob) ) Nonitonella atlantica = NV. species A Oolina apiculata = O. lineata (Williamson) Planorbulina mediterranensis = P. distoma Terquem Protelphidium depressulum = P. anglhicum Murray Protoschista findens = keophax monitlforme Siddall Pyrgo williamsoni = P_ species: A Quingueloculina agglutinata = Q. aspera da’ Orbigny Quinqueloculina subarenaria = Q. aspera d’Orbigny Quinqueloculina species 3 = Q. lata Terquem Spirillina vivipara = S. perforata (Schultze) Species represented by single, imperfect specimens are not described. In addition all the species of Lenticulina and all species of Cassidulina except one are set aside — until better material is obtained from deeper parts of the Irish Sea. 3. No attempt is made to arrange the species in groups above the family level. 4. Although the fundamental character of the wall is valuable in classification it cannot be applied rigidly. It seems unlikely that all the different wall structure groups arose separately from tectinous ancestors. In particular, optically granular structure is near to radial structure and one may derive from the other. For this reason, the attempt to hive off granular forms into the three supe families Cassidu- linacea, Anomalinacea and Nonionacea is abandoned. 5. The family Nonionidae is interpreted in the wide sense to include both Nomon and Elphidium. Elphidium is interpreted widely to include radial and granular species both with and without septal bridges and fossettes. 6. The family Discorbidae is interpreted in the wide sense and some recently | suggested generic names, Glabratella, Neoconorbina and Gavelinopsis, are used only | tentatively or abandoned. Much more needs to be known about wall structure | and reproduction before further names are coined for the ‘discorbids’. | | CARDIGAN BAY RECENT FORAMINIFERA 221 VIIL---REFERENCES Acosta, J. T. 1940. Algunos Foraminiferos nuevas de las costas Cubanos. Torreia 5 : 3-6. Apams, T. D. +4963. Holocene foraminifera from the Dovey Estuary and Cardigan Bay. Un- published Ph.D. thesis, Univ. Coll. of Wales. Apams, T. D. & FRAMPTON, J. 1965. A note on some recent foraminifera from North west Iceland. Contr. Cushman Fdn. Foramin. Res. 16 (2) : 55-59, pl. 5, 1 tf. Apams, T. D. & Haynes, J. 1965. Foraminifera in Holocene marsh cycles at Borth, Cardi- ganshire (Wales). Palaeontology 8 : 27-38. Apams, T. D., HAYNEs, J. R. & WALKER, C. T. 1965. Boron in Holocene illites of the Dovey Estuary, Wales and its relationship to palaeosalinity in cyclothems. Sedimentology 4 : 189- 195. ADEGOKE, O. S., DESSAUVAGIE, T. F. J. & YoLoveE, V. L.A. 1969. 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Temperature and depth distribution of some Recent and fossil fora- minifera in the southern California region. Bull. Scripps Instn. Oceanogr. tech. Ser. 3 (10) : 225-330, 1 tab., I map. ——— 1938. New species of foraminifera from off the west coast of N. America and from the later Tertiary of the Los Angeles Basin. Cal. Univ. Bull. Scripps Instn. Oceanogr. tech. Sev. 4 (5) : 137-164, pls 3-7. Norin, E. 1958. The sediments of the Central Tyrrhenian Sea. Rep. Swed. deep Sea Exped. Vol. 8. Sediment cores from the Mediterranean Sea and the Red Sea 1 : 3-136, pls 1-19. Norman, A.M. 1878. On the genus Halyphysema with a description of several forms apparently allied to it. Ann. Mag. nat. Hist. ser. 5, 1 : 265-284, pl. 16. Norvanc, A. 1941. Notes on some Foraminifera from off Bergen. Naturvitons kapelig vekke 11 : 3-10, 3 tfs. 1945. The zoology of Iceland pt. 2, 2 : 1-79, 13 tis, 2 tabs. Copenhagen and Reykjavik. 1966. Textilina nov. gen., Textularia Defrance and Spiroplectammina Cushman (Foramint- fera): Biol. Sky. 19\(3\c 1-10, pls a,12) Nyuoitm, K.-G. 1961. Morphogenesis and biology of the foraminifer Cibicides lobatulus. Zool. Bidy. Upps. 33 : 157-196, pls I-5. ) : D’Orpicny, A. D. 1826. Tableau méthodique de la classe des Céphalopodes. Amn. Se. Nat. Paris. ser. 1, 7 : 96-132. 1839a. Foraminiféres. In: Sagra, R. de la, Histoive physique, politique et naturelle de Visle de Cuba. Paris, A. Bertrand, 224 pps (plates pub. separately). 1839b. Foraminiféres des Isles Canaries. In: Barker-Webb, P. & Berthelot, S., Histoire Naturelle des Iles Canaries. Paris, Béthune. 2 (2) Zool. : 119-146, pls 1-3. CARDIGAN. BAY. RECENT FORAMINIFERA 233 D’OrBiGNy, A. D. 1839c. Voyage dans l Amérique Méridionale: Foraminifeves. Strasbourg, P. Bertrand. 5 (5) : 1-86, pls 1-9. —— 1846. Foraminiféres fossiles du bassin Tertiaire de Vienne. Gide et Comp. Paris. 1-303 pls 1-21. Ovey, C. D. 1948 (reprint 1950). Some ecological aspects of the foraminifera and their application to stratigraphy. S. East Nat. 53 : 39-47, 1 pl. ParFitt, E. 1878. On the structure of Haliphysema tumanowiczii. Ann. Mag. nat. Hist. ser. 5, 2 : 88-90. - ParKER, F. L. 1948. Foraminifera of the Continental Shelf from the Gulf of Maine to Mary- land. Bull. Mus. comp. Zool. Harv. 100 (2) : 213-241, 7 pls. 1952a. Foraminifera species off Portsmouth, New Hampshire. Bull. Mus. comp. Zool. Harv. 196 (9) : 391-423, 6 pls. — 1952b. Foraminiferal distribution in the Long Island Sound—Buzzards Bay area. Bull. Mus. comp. Zool. Harv. 106 (10) : 428-473, 5 pls. 1954. Distribution of the foraminifera in the north eastern Gulf of Mexico. Bull. Mus. comp. Zool. Harv. 111 (10) : 453-588, pls 1-13. —— 1958. Eastern Mediterranean foraminifera. Rep. Swed. deep Sea Exped. 8 (Sediment cores from the Mediterranean Sea and the Red Sea 4) : 219-283, tabs. — — 1960. Living planktonic foraminifera from the equatorial and southeast Pacific. Sczent. | Rep. Tohoku Univ. ser. 2, Spec. vol. 4 : 71-82. — 1962. Planktonic foraminiferal species in Pacific Sediments. Mzcropalaeontology 8 (2) : 219-254, pls I-Io. —— 1967. Late Tertiary Biostratigraphy (Planktonic Foraminifera) of Tropical Indo-Pacific Deep Sea Cores. Bull. Am. Paleont. 52 (235) : 115-208, pls 17-32. PARKER, F. L. & ATHEARN, W. D. 1959. Ecology of marsh foraminifera in Poponesset Bay, Massachusetts. J. Paleont. 33 (2) : 333-343, 5 tfs, 1 pl. PARKER, F. L., PHLEGER, F. B. & PErRsSoN, J. F. 1953. Ecology of foraminifera from San Antonio Bay and environs, Southwest Texas. Cushman Fdn. Foramin. Res., Spec. Pub 2: 1-75, pls 1-4, tfs 1-48, tabs 1-7. PARKER, W. K. (in Dawson, G. M.). 1870. On Foraminifera from the Gulf and River St Lawrence. Can. Naturalist n.s. 5 : 172-180. PARKER, W. K. & Jones, T. R. 1857. Descriptions of some Foraminifera from the Coast of Norway. Ann. Mag. nat. Hist. ser. 2, 19 : 273-303, pls 10, If. — 1859. On the nomenclature of the Foraminifera. Pt. 2. On the species enumerated by Walker and Montagu. Ann. Mag. nat. Hist. ser. 3, 4 : 333-351. |—— 1863. On the nomenclature of the foraminifera. Pt. 10. The species enumerated by d’Orbigny in the ‘Annales des Sciences Naturelles’, vol. 7, 1826. Ann. Mag. nat. Hist. | ser. 3, 12 : 429-441. —— 1865. On some foraminifera from the North Atlantic and Arctic oceans including the Davis Straits and Baffin Bay. Phil. Trans. R. Soc. 155 : 325-441, pls 13-19, 12 tabs, map. *ARKER, W. K., JoNES, T. R.& BRapy,H.B. 1865. Onthe nomenclature of the foraminifera. Pt. 12 (misprinted as pt. X continued). The species enumerated by d’Orbigny in the ‘Annales des Sciences Naturelles’, vol. 7, 1826. Ann. Mag. nat. Hist. ser. 3, 16 : 15-41, pls 1-3. '—— 1871. On the nomenclature of the foraminifera. Pt. 14. The species enumerated by d’Orbigny in the ‘Annales des Sciences Naturelles’, 1826, vol. 7 (continued from Aun. | Mag. nat. Hist. ser. 3, 16: 41). Ann. Mag. nat. Hist. ser. 4, 8 : 145-179; 238-266, pls 8-12. ARR, W. J. 1950. Foraminifera. Rep. B.A.N.Z. Antarctic Res. Exped. 1929-31 ser. B. (Zool. & Bot.), 5 (6) : 236-392, 13 pls, 8 tfs. |BARCEY, F.G. 1881. Foraminifera. In: Herdman, W.A., Additional notes on the inverte- _. brate fauna of Lamlash Bay, Isle of Arran. Proc. R. phys. Soc., Edinb. 6 : 17-30. 234 J; Keen AYNEES PreARCEY, F. G. 1890. Notes on the foraminifera of the Faroe Channel and Wyville Thompson Ridge with a description of a new species of Hypevammina. Proc. Trans. nat. Hist. Soc. Glasg. n.s. 2 (1886-1888) : 163-179, pl. 3 1891. Notes on the foraminifera dredged by the L.M.B.C. in Liverpool Bay during 1890. In: Herdman, W. A., 4th A. Rep. Puffin Isl. biol. Stat. and the L.M.B.C.; Append. Proc. Trans. Lpool. biol. Soc. 5 ; 58-61. 1902. Notes on the marine deposits of the Firth of Forth and their relation to its animal life. Proc. Trans. nat. Hist. Soc. Glasg. n.s. © : 217-251, I map. 1914. Foraminifera of the Scottish National Antarctic Expedition. Tvans. R. Soe. Edinb. 49, pt. 4, (19) : 991-1044, 2 pls. PHLEGER, F. B. 1952a. Foraminifera ecology off Portsmouth, New Hampshire. Bull. Mus. comp. Zool., Harv. 106 (8) : 315-390, 26 tfs, 18 tabs. 1952b. Foraminifera distribution in some sediment samples from the Canadian and Greenland Arctic. Contr. Cushman Fdn. Foramin. Res. 3 (2) : 80-89, pls 13, 14, tab. and map. . 1954. Ecology of Foraminifera and associated micro-organisms from Mississippi Sound and environs. Bull. Am. Ass. Petrol. Geol. 38 (4) : 584-647, pls 1-3, 28 tfs. 1955. Ecology of foraminifera in S.E. Mississippi Delta Area. Bull. Am. Ass. Petyol Geol. 39 (5) : 712-752, 40 tfs. 1956. Significance of living foraminiferal populations along the Central Texas Coast. Contry. Cushman Fdn. Foramin. Res. 7 (4) : 106-151, 20 tfs, 11 tabs. 1960a. Sedimentary patterns of microfaunas in Northern Gulf of Mexico. In: Recent Sediments, N.W. Gulf of Mexico 1951-1958, pp. 267-381, pls 1-6, 16 tfs. Am. Ass. Petrol. Geol. Tulsa, Okla. 1960b. Ecology and distribution of Recent foraminifera. 297 pps, 11 pls, tis 83. John Hopkins Press, Baltimore. 1965. Patterns of marsh foraminifera, Galveston Bay, Texas. Limmnol. Oceanogr. 10; R169-R184. 1966. Patterns of living marsh foraminifera in South Texas coastal lagoons. Boln. Soc. Geol. mex. 28 (1) : 1-44, tis 1-22, Io tabs. 1967. Marsh foraminiferal patterns, Pacific Coast of North America. An. Inst. Biol. Uni. Mex. 38. Ser. Cienc. Del. Marv Y Limnol. (1) : 11-38, tfs 1-19, 5 tabs. PHLEGER, F. B. & BrapvsHaw, J. S. 1966. Sedimentary environments in a marine marsh. Science N.Y. 154 (3756) : 1551-1553. PHLEGER, F. B. & Lanxrorp, R. L. 1957. Seasonal occurrences of living benthonic Fora- minifera in some Texas Bays. Contr. Cushman Fdn. Fovamin. Res. 8 (3) : 93-105, 6 tis. PHLEGER, F. B. & Parker, F. L. 1951. Ecology of foraminifera, northwest Gulf of Mexico. Pt. 2. Foraminifera Species. Mem. geol. Soc. Am. 46 : 1-64, pls 1-20. 1952. New names for North Western Gulf of Mexico, Foraminifera. Conty. Cushman Fdn. Fovamin. Res. 3 (1) : 14. PHLEGER, F. B., PARKER, F. L. & Petrson, J. F. 1953. North Atlantic foraminifera. Rep. Swed. deep Sea Exped. 7 (1) : 3-122, pls 1-12, tfs 1-26. PHLEGER, F. B. & Watton, W.R. 1950. Ecology of marsh and bay foraminifera, Barnstable, Mass. Am. J. Sci. 248 : 274-294. Potski, W. 1959. Foraminiferal biofacies of the North Asiatic coast. J. Palaeont. 33 (4) : 569-587, pl. 78, 8 tfs. ReEADE, T. M. 1900. A contribution to post-glacial geology, Foraminifera of the Formby and Leasowe Marine Beds. Geol. Mag. 7 : 97-105, 1 pl. Reiss, Z. 1959. The wall structure of Cibicides, Planulina, Gyroidinoides and Globorotalites. Micropalaeontology 5 (3) : 355-356, 1 pl. pls 1-8. Reiss, Z., Ktuc, K. & MERLING, P. 1961. Recent Foraminifera from the Mediterranean and i Red Sea coasts of Israel. Bull. geol. Surv. Isvael 32 : 27-28. ee 1963. Reclassification of perforate Foraminifera. Bull. geol. Surv. Isvael 35: 1-111, i CARDIGAN BAY RECENT FORAMINIFERA 235 Reuss, A. E. 1844. Geognostische Skizzen Bohem. Prag, C. W. Medau, 2, 304 pps, 3 pls. 1850. Neues Foraminiferen aus den Schichten des ‘osterreichischen Tertiarbeckens. K. Akad. Wiss. Wien. Math._—Naturw. CI 1 : 365-390, pls 46-51, 1862. Entwurf einer systematischen Zusammenstellung der Foraminiferen. K. Akad. Wiss. Wien. Math.—Naturw. Cl. 44 (1861) 1 : 395-396. 1863. Die Foraminiferen-Familie der Lagenideen. Sbev. Akad. Wiss. Wien. math.—nat. Kl. 46 (1) : 308-342, pls 1-7. RHUMBLER, L. 1906. Foraminiferen von Laysan und den Chatham-Inseln. Zool. Jb. 24 : 21-80, pls 2-5. '—— t911. Die Foraminiferen (Thalamophoren) der Plankton—Expedition; Erster Teil: Die allgemeinen Organizationsverhaltnisse der Foraminiferen. Plankton—Exped. Hum- boldt-Stiftung. Evgeb., Kiel u. Leipzig 3 (Lc) : 1-331, pls 1-39, tfs 1-110. -—— 1913. Die Foraminiferen (Thalamophoren) der Plankton—Expedition; Zweiter Teil; Systematik. Plankton—Exped. Humboldt-Stiftung, Evgeb., Kiel u. Leipzig 3 (Lc) : 333- 470, tis 111-175. 1938. Foraminiferen aus dem Meeressand von Helgoland. SKuieley Meeves forsch. 2 : 157- 222, tis 1-64. RispaLt, Dac. 1963. The foraminiferal fauna in some cores from inner Oslo Fjord. Norg. geol. Unders. 224 : 1-90, tfs 1-7. Risso, A. 1826. Histoire naturelle des principales productions de l’Euvope Méridionale. | Paris. F.G. Levrault. 4: 1-439, pls 1-12. -Ropertson, D. 1870. ‘Foraminifera’ in Report of the Committee appointed to explore the marine fauna and flora of the South coast of Devon and Cornwall. No. 3. Rep. By. misss Aavmt. Sct., (Exeter) 1860, p. Of. 1877. Notes on the Recent Ostracoda and foraminifera of the Firth of Clyde with some remarks on the distribution of the Mollusca. Tvans. geol. Soc. Glasg. 5 : 112-153, tab. -—— 1883. Report on the sands and gravels and boulder clays in the top silt at Dock F of the Atlantic Docks, Liverpool. Appendix to T. M. Reade: The Drift Beds of the Northwest of England and North Wales. Q. J. geol. Soc. Lond. 39 : 129-132. 1892. List of foraminifera dredged in Portree Bay, Island of Skye. Proc. Tvans. nat. Hist. Soc. Glasg. n.s. 3 : 239-242. —— Igor. Foraminifera. In: Fauna, flora and geology of the Clyde area. British Assoc. | Handb., pp. 376-383. Ropertson, D. & BRapy, G.S. 1876. Report on the dredging off the coast of Durham and | North Yorkshire in 1874. Rep. By. Ass. Advmt. Sci., (Bristol) 1875, pp. 185-199. ‘Ronat, P. H. 1955. Brackish water foraminifera of the New York Bight. Contr. Cushman Fdn. Foramin. Res. 6 (4) : 140-149, pls 20, 21, I tab. RUSCELLI, M. 1949. Foraminiferi di Due saggi di Fondo del Mar Ligure. Jnst. Geol. Pal. Geog. Fis. Univ. Studi Milano Ser. P. 62 : 1-31, 2 pls. Rutten, L. & Hotz, W. 1946. Geological, Petrographical and Palaeontological Results | of exploration carried out from September 1917 until June 1919 on the Island of Ceram. J. de Bussy, ser. 3 (Geol.) 2 (J. H. Germeraad Geology of Central Ceram.) : 42-79, 4 tabs, 6 pls. pl-30, fig. 3 willamsoni, 162; Pl. 17, figs 13-15 species A, 163; Pl. 17, fig. ro ROTALIIDAE, 184 rugosa, Quiqueloculina cf., 74; Pl. 7, figs 20, 21 SACCAMMINIDAE, 18 sachalinica, Cibicides fletcheri, 172; figs 1,°2 scabrum, Eggerelloides, 44; Pl. 2, figs 7, 8, pl: 19, figs: 10,-1T Scutuloris, 76 species A, 76; Pl. 9, fig. 14 sécans, Masstlina, 53; Pl. 5, figs 3, 4, pl. 8, Hee On ply a2, tio, 4 selseyensis, Cyclogvra, 48; Pl. 9, fig. fig. 4 selseyense, Elphidium, 204; Pl. 22, figs 3, 4, ple 24, 1S 11, pl.-20; figs 4,.5) 7,0, 10, pk: 29, figs 1-3 seminulum, Quinqueloculina, 74; Pl. 7; figs 14, 10, pl. 8, fig. 3, pl. 32, figs1—3 semistriata, Lagena, 87; Pl. 12, fig. 6, pl. 13, fig. 4 Sigmoilopsis, 77 moyt, 77; Pl. 4, figs 1-8, pl. 8, figs 5, 7 Siphonina, 167 georgiana, 167; Pl. 20, figs 15, 16, pl. 23, fig. 9, pl. 33, fig. 10 SIPHONINIDAE, 167 spathulata, Bolivina, 135 spicata, Lagena, 88; Pl. 12, fig. 13 Spivrillina, 144 perforata, 144; Pl. 15, fig. 9, pl. 16, figs 1, 2 species A, 144; Pl. 15, fig. 10, pl. 16, figs. 5,6 SPIRILLINIDAE, 142 Spiroloculina, 78 depressa, 78; Pl. 9, figs 6, 7 Spivoplectammina, 31 caviand?, 31; Pl. 3, fig. 5, pi: 3, fig. “11 wright, 32; Pl. 3; figs 1, 2 Spivopthalmidium, 50 acutimargo var. emaciatum, 50; Pl. 5, fig. Ei, pl.o, ig. 16 squamosa, Oolina, 110; Pl. 14, fig. 14, pl. 15, figs 4, 5 Stainforthia, 123 concava var. loeblichi, 123; Pl. 5, fig. 10 fustformis, 124; Pl. 5, figs 7, 8 species A, 126; Pl. 5, fig..9, pl. 8, fig. 4 styviata, Lagena, ef.,.89:; Pl,,72, fig’ r2,-pl:' 13, figs 7, 8 siviaiula, Bohvina, 137; Pl..1z0, fig. 1; pl. -21, fig. I suboblonga, Pseudopolymorphina, 113 subrotunda, Miliolinella, 56; Pl. 5, figs 5, 6, pl. 31, figs 8, 9 subrotunda pateorid var., Miliolinella, 57; Pls; figs 12,.13 Ph, 21, TP, pl. 29, 244 substriata, Lagena, 89; Pl. 12, fig. r1, pl. 13, figs 6, II sulcata, Lagena, 90; Pl. 12, fig. 9, pl. 13, fig. 10 sulcata interrupta, Lagena, 92; Pl. 12, fig. 10 sulcata var. torquiformis, Lagena, 93; Pl. 52, fig,-14, pl. 13; figs.9, 12 superba, Bolivina, 138; Pl. 10, fig. 5, pl. 11, figs 2, 3 Technitella, 17 teivyense, 17; Pl. 1, figs 1-4 teivyense, Technitella, 17; Pl. 1, figs 1-4 tepida, Ammonia, 191; Pl. 18, fig. 17, pl. 30, fig. 8 Textilina, 47 bocki,. 47. Pli3, figs 6, 7, pl./8;.e. 8 Textularvidae, 31 torquiformis, Lagena sulcata, 93; Pl. 12, fie 14, pli 13: figs: 9,12 Trifarina angulosa, 126; Pl. 10, figs 12, 13, 16, 075, pl: TV; fig. 7k tvigonula, Triloculina, 79; Pl. 9, figs 1, 2, pl. 32, fig. 5 tvihedva, Triloculina, 80; Pl. 9, figs 3, 4 Triloculina, 79 trigonula, 79; Pl. 9, figs I, 2, pl. 32, fig. 5 tyithedrva, 80; Pl. 9, figs 3, 4 Trochammina, 34 astyifica, 34; Pl. 4, figs 18-20 haynes, 35 globigeriniformis var. pygmaea, 36; Pl. 4, fig. 14 inflata, 37; Pl. 4, figs 15-17, pl. 6, fig. 3 intermedia, 39; Pl. 4, figs 9-13, pl. 6, fig. 9 INDEX ochracea, 40; Pl. 5, figs 15-18 TROCHAMMINIDAE, 34 tvondheimensis, Dentalina ci., 80; Pl. 16, fig. II . tumanowicz, Halyphysema, 14; Pl. 1, fig. 6, pl 2e he 13 turgida, Nonionella, 213; Pl. 22, fig. 12 turgida var. digitata, Nonionella, 214 TURRILINIDAE, 114 Turrispirillina, 145 species A, 145; Pl. 16, figs 3, 4 universa, Orbulina, 184; Pl. 20, fig. 6 UVIGERINIDAE, 126 — vadescens, Bolwina ci., 139; Pl. 10, fig pleir, Le 9 variabilis, Bolivina, 141; Pl. to, fig. 8, pl. 11, fig. 8 waddensis, Elphidium, 206; Pl. 24, figs 4, ro, pl. 26; fig. 1, pl. 28, fies. 16,410 wilberti, Haplophragmoides, 27; Pl. 2, fig. 1, DEeZo, e177 williiamsoni, Elphidium, 207; Pl. 24, fig. 7, pl. 25, figs 6, 9, pl. 27, figs 1-3 williamsont, Oolina, 111; Pl. 14, figs 15-17, Plei5,.Hes 1, 2.7, wiliamsoni, Rosalina, 162; Pl. 17, figs 13-15 wilhramsoni, Pyrgo, 61 wrightit, Discorbis, 147; Pl. 16, figs 12-16, pl. 19, fig. 5, pl. 30, figs 4, 5 wrighti1, Spiroplectammina, 32; Pl. 3, figs 1, 2 x. ADDENDUM References cited but inadvertently left out of Part VIII include: Atkinson, K. 1968. A taxonomic note on Massilina carinata (Fornasini 1905) Contr. Cushman Fdn. Foramin. Res. 19 : 165-167, tfs 1-3. Dupeuble-.2> a 10962, Région de Roscoff (Finistére). Polymorphisme chez les Cibicidinae Actuels de la ~ Revue Micropaléont. 4 (4) : 197-202, pls I, 2. Two importart works on British Recent Foraminifera which came to hand after going to press include: Atkinson; K.- 97x, lhe relationship of Recent Foraminifera to the sedimentary facies in the turbulent zone, Cardigan Bay. J. nat. Hist. 5 : 385-439, tfs I-14. Murray, J. W.. 21077. 244 pp., 96 pls. An Atlas of British Recent Foraminiferida. Heinemann, Atkinson’s paper went to press before we had finished our revision of nomenclature so his names require correction as indicated in Part VIL. The same applies to the names in the ‘Atlas’ where ‘accepted British usage’ has been followed. However, Se a “ ADDENDUM 7 245 Murray has made certain innovations, and two in particular are unacceptable in our opinion. These are the attempt to subsume E/phidiwm selseyense under E. excavatum and to place the species called F. excavatwm by British workers under E. articulatum (d’Orbigny). As we have shown (pages 206 and 208) E. selseyense can be distin- guished from E. evcavatum as redefined by Lévy ef al. (1969). Further, as it has proved impossible to find an unambiguous early name for EF. excavatwm of authors’ —Polystomella umbilicatula of Williamson, this species is renamed by us E. william- sont. To place this form under FE. articulatum would only make the confusion worse. D’Orbigny’s species was described from the coast of Patagonia and the Falklands. The type specimen is lost as was discovered by Heron, Allen and Earland (1932) when they examined d’Orbigny’s tube in the Musée d’Histoire Naturelle, Paris. However, the type figure shows a lobate species with inflated chambers, small septal pits and areal apertures in a concave apertural face; clearly different from E£. excavatwm of authors’ which is entire, flat-sided and characterized by oblong fossettes. Specimens figured by Cushman as F. articulatum in the Atlantic Monograph (1930) are similar to d’Orbigny’s figure although they do not show the areal apertures. It is significant that Cushman distinguished between this species and FE. excavatum in the same Monograph and maintained this distinction later. FE. excavatum is well figured from the Belgian coast (1949) whereas the only reference to d’Orbigny’s species in the North Atlantic is of doubtful material from off New England, as E. cf. articulatum (1944). In the circumstances the best course seems to be to apply a new name to the brackish water, N. European species. At least there is little doubt that this is the form figured by Williamson. Joun RoLanp Haynes, Ph.D., F.G:S. TERENCE DaAvip ADAMS, Ph.D., F.G.S. Depaviment of Geology BRITISH PETROLEUM COMPANY LTD. UNIVERSITY COLLEGE OF WALES B.P. House PENGLAIS ROPEMAKER STREET ABERYSTWYTH, CARDIGANSHIRE Lonpbon, E.C.z2 KEITH ATKINSON, Ph.D., C.Eng., ~ DREW Haman, Ph.D., F.G.S. A.M.I.M.M., F.G.S. STANDARD OIL OF CALIFORNIA CAMBORNE SCHOOL OF MINES P.O. Box 7-839 CAMBORNE ANCHORAGE CORNWALL ALASKA 99501 EMMANUEL ABIODUN FayosgE, M.Sc., Ph.D. KeitH HavarpD JAMES, D.U.C.W., M.Sc. Department of Geology Department of Geology UNIVERSITY OF IBADAN UNIVERSITY COLLEGE OF WALES IBADAN PENGLAIS NIGERIA ABERYSTWYTH, CARDIGANSHIRE Joan ANNE JouNson, M.Sc. Joun Scott, M.Sc., Ph.D. The Library Department of Geology UNIVERSITY OF LANCASTER UNIVERSITY COLLEGE BAILRIGG GOWER STREET _ LANCASTER Lonpon, W.1 PLRATE x: Fics 1-4. Technitella teivyense Haynes n. sp. 1, holotype, stereopair showing aperture — and open spicular structure x 65; 2, side view xX 60; 3, paratype showing brushed forward © spicules x< "5,250; 7, aperture. << n100. Fic. 6. Remaneica helgolandica Rhumbler, detail of umbilicus and chamber lobes x 1050. Fic. 8. Reophax moniliforme Siddall, detail of aperture x 525. Fic. 9. Tvochammina intermedia Rhumbler ? detail of wall x I1o0o. Fic. 10. ? Marstpella species A, detail of wall x 265. Fic. 11. ? Marsipella species B, detail of wall x 140. Bull. Br. Mus. nat. Hist. (Zool.) Suppl. 4 PLA LE..6 PLATE 7 Fics 1-3. Quinqueloculina aspera d’Orbigny. 1, oblique apertural view of slightly irregular - specimen X 65; 2, 3, front view and apertural view of more regular form x 55. Fics 4, 5. Quinqueloculina mediterranensis Le Calvez & Le Calvez, specimen described. 4, rear view showing periphery x 55; 5, apertural view x 60. Fics 6, 7. Quinquelcculina auberiana var. B, specimen described. 6, oblique front view xX 65; 7, apertural view xX 70. Fics 8, 9. Quinqueloculina cf. chavrensis Heron-Allen & Earland. 8, front view x 55; Q, apertural view X 45. Fics 10-13. Quinqueloculina lata Terquem. 10, 11, front view and apertural view of juvenile x 105 (QO. species 3); 12, 13, front view and apertural view of specimen described x 40. - Fics 14,19. Quinqueloculina seminulum (Linnaeus). 14, apertural view x 70; 19, probable juvenile, front view xX 130. Fic. 15. Quinqueloculina auberiana var. A. Front view of specimen described x 65. Fics 16,17. Quinqueloculina intricata Terquem. 16, front view of specimen described x 45; 17, juvenile with one chamber following the juvenarium x 45 Fic. 18. Quinqueloculina bicornis (Walker & Jacob), front view of neotype x 55. Fics 20, 21. Quinqueloculina cf. vugosa d’Orbigny, front view and apertural view of specimen described 65. Fics 22, 23. Quinqueloculina cf. duthiersi (Schlumberger), rear view and apertural view of — | specimen described x 25. ~ SALTS nat Dis Vu WE. BY... 1 PLATE 8 Fic. 1. Quinqueloculina mediterranensis Le Calvez & Le Calvez, detail of aperture x 300. Fic. 2. Quinqueloculina aspera d’Orbigny, detail of aperture x 275. Fic. 3. Quinqueloculina seminulum (Linneaus), detail of tooth x 575. Fic. 4. Stainforthia species A, detail of aperture x 475. Fics 5,7. Sigmoilopsis moyi Atkinson. 5, detail of aperture x 850; 7, detailed wall structure xX 525. Fic. 6. Massilina secans (d’Orbigny), detail of aperture x 120. Fic. 8. Textilina bocki (Hoglund), detailed wall structure x 1060. Fic. 9. Cribrostomoides jeffreysi (Williamson), close up showing wall structure inthe umbilical area and the projecting apertural lip x 265. Fic. 10. Lagenammina cf. hancocki (Cushman & McCulloch), aperture and fine structure of the lip’ +525. Fic. 11. Spivoplectammina earlandi (Parker), aperture and wall structure x 500. Fic. 12. Lagenammina avenulata (Skinner), detail of aperture x 500. 4 ) Suppl ool. Zi ( MeElasts nat S Mu io Bull. iH PEA Eo Fics 1, 2. Triloculina trigonula (Lamarck), front view and apertural view of specimen described x I00. . Fics 3, 4. Tvriloculina trihedva Loeblich & Tappan, front view and oblique apertural view of specimen described x 120. | Fic. 5. Quinqueloculina cf. chavensis var. A, front view of specimen described x 55. | Fics 6, 7. Spiroloculina depressa d’Orbigny, front view and apertural view of specimen | described x 65. : 4 Fics 8,9. Pyrgo species B, front view and apertural view of specimen described x 105. Fics 10, 13. Pyrgo species A, front view and apertural view of specimen described x I05. Fics 11, 12. Pyrgo cf. constricta Costa, front view and apertural view of specimen described | ee yeaearses a it ol pe yak ee ta oe wavelet Bekaae . titers! ares at hoa oats od ve vt ot Cx eeu ane i= ot ent " er : Gest eeet ; ; : . years : oe : s ar : . 4 aoe - : a} ss ae . ‘ . 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