VOLUME 77 PART 7 OF THE SOUTH AFRICAN MUSEUM CAPE TOWN INSTRUCTIONS TO AUTHORS 1. MATERIAL should be original and not published elsewhere, in whole or in part. 2. LAYOUT should be as follows: (a) Centred masthead to consist of Title: informative but concise, without abbreviations and not including the names of new genera or species Author’s(s’) name(s) : Address(es) of author(s) (institution where work was carried out) Number of illustrations (figures, enumerated maps and tables, in this order) (b) Abstract of not more than 200 words, intelligible to the reader without reference to the text (c) Table of contents giving hierarchy of headings and subheadings (d) Introduction ‘ é ; (e) Subject-matter of the paper, divided into sections to correspond with those given in table of contents (f) Summary, if paper is lengthy (g) Acknowledgements (h) References (i) Abbreviations, where these are numerous 3. 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For books give title in italics, edition, volume number, place of publication, publisher. For journal article give title of article, title of journal in italics (abbreviated according to the World list o, scientific periodicals. 4th ed. London: Butterworths, 1963), series in parentheses, volume number, part number (only if independently paged) in parentheses, pagination (first and last pages of article). Examples (note capitalization and punctuation) BULLOUGH, W. S. 1960. Practical invertebrate anatomy. 2nd ed. London: Macmillan. FISCHER, P.—H. 1948. Données sur la résistance et de le vitalité des mollusques. J. Conch., Paris 88: 100-140. FIscHER, P.-H., DuvAL, M. & Rarry, A. 1933. Etudes sur les échanges respiratoires des littorines. Archs Zool. exp. gén. 74: 627-634. Konn, A. J. 1960a. Ecological notes on Conus (Mollusca: Gastropoda) in the Trincomalee region of Ceylon. Ann. Mag. nat. Hist. (13) 2: 309-320. Koun, A. J. 19606. Spawning behaviour, egg masses and larval development in Conus from the Indian Ocean. Bull. Bingham oceanogr. Coll. 17 (4): 1-51. THIELE, J. 1910. Mollusca: B. Polyplacophora, Gastropoda marina, Bivalvia. In: SCHULTZE, L. Zoologische und anthropologische Ergebnisse einer Forschungsreise im westlichen und zentralen Siid-Afrika 4: 269-270. Jena: Fischer. Denkschr. med.-naturw. Ges. Jena 16: 269-270. (continued inside back cover) ANNALS OF THE SOUTH AFRICAN MUSEUM ANNALE VAN DIE SUID-AFRIKAANSE MUSEUM Volume 77 Band February 1979 February Part 4 Deel A NEW GENUS AND SPECIES OF THE PENAEOID FAMILY SOLENOCERIDAE (CRUSTACEA, DECAPODA) FROM SOUTH-EAST AFRICAN WATERS By ANTONIO J. DE FREITAS Cape Town Kaapstad The ANNALS OF THE SOUTH AFRICAN MUSEUM are issued in parts at irregular intervals as material becomes available Obtainable from the South African Museum, P.O. Box 61, Cape Town 8000 Die ANNALE VAN DIE SUID-AFRIKAANSE MUSEUM word uitgegee in dele op ongereelde tye na beskikbaarheid van stof Verkrygbaar van die Suid-Afrikaanse Museum, Posbus 61, Kaapstad 8000 OUT OF PRINT/UIT DRUK 1, 2(1-3, 5-8), 3(1-2, 4-5, 8, t.—p.i.), 5(1-3, 5, 7-9), 6(1, t.-p.i.), 711-4), 8, 9(1-2, 7), 10(1-3), 11(1-2, 5, 7, t.—p.i.), 15(4-5), 24(2), 27, 31(1-3), 32(5), 33 Copyright enquiries to the South African Museum Kopieregnavrae na die Suid-Afrikaanse Museum ISBN 0 908407 64 5 Printed in South Africa by In Suid-Afrika gedruk deur The Rustica Press, Pty., Ltd., Die Rustica-pers, Edms., Bpk., Court Road, Wynberg, Cape Courtweg, Wynberg, Kaap A NEW GENUS AND SPECIES OF THE PENAEOID FAMILY SOLENOCERIDAE (CRUSTACEA, DECAPODA) FROM SOUTH-EAST AFRICAN WATERS By ANTONIO J. DE FREITAS Oceanographic Research institute, Durban (With 1 figure and 1 table) {MS accepted 31 October 1978] ABSTRACT A new genus, Cryptopenaeus, is proposed for a new solenocerid species, Cryptopenaeus catherinae, which is described and illustrated. The new genus is related to Hymenopenaeus and Haliporoides formerly belonging to the genus Hymenopenaeus, sensu lato. C. catherinae has so far been found only in three localities off southern Mozambique at depths of 310-500 metres. CONTENTS PAGE Introduction Gera bia dem aint Oe ES, Cryptopenaeus gen. nov. . : ; 2. 423 Cryptopenaeus catherinae sp. nov. . 5 aes} Acknowledgements . : ; : . 130 IReferencesi= a) ean pean ee e130 INTRODUCTION In June 1969, while collecting penaeoid shrimps aboard a trawler operating in deep water off southern Mozambique, one male specimen representing a new genus and species was caught in 350 metres of water. Further male specimens were subsequently found in the same area in June 1973, and the only female available was caught in September 1976 at a depth of 500 metres. All specimens were caught together with the commercially important pink or knife prawn Haliporoides triarthrus, as well as the less common Aristeomorpha foliacea and Penaeopsis balssi. Genus Cryptopenaeus gen. nov. Diagnosis Body robust; carapace elongate; integument firm. Rostrum short, not reaching distal margin of first antennular segment; ventral margin moderately convex; armed only with dorsal teeth; epigastric tooth and first rostral separated by interval equal to or only slightly greater than that between first and second rostral teeth. Orbital, suprahepatic and branchiostegal spines absent; antennal, postorbital, hepatic and pterygostomian spines present; cervical sulcus deep, long but not reaching mid-dorsum of carapace; hepatic sulcus deep and long, bending anteroventrally from horizontal posterior part and almost reaching 123 Ann, S. Afr. Mus. 77 (7), 1979: 123-131, 1 fig., 1 table. 124 ANNALS OF THE SOUTH AFRICAN MUSEUM base of pterygostomian spine; orbito-antennal groove shallow and wide; branchiocardiac carina distinct but not sharp; mid-dorsal abdominal carina present on segments two to six. Telson with pair of short fixed spines ; no movable marginal spines. Prosartema narrow, long, extending beyond end of eye. Antennular flagella similar, subcylindrical and equal to, or slightly longer than, carapace. Mandibular palp two jointed; articles subequal in length, distal one narrower than basal and tapering to rounded apex. Exopodites on all maxillipeds and pereiopods. Lateral ramus of uropod with very small, blunt distolateral spine. Petasma with ventrolateral lobule entirely occupied by ventral costa and distally free from dorsolateral lobule; both ventrolateral and dorsolateral lobules heavily sclerotinized ; appendix masculina and appendix interna present. Thelycum simple, of open type. Podobranch on maxilliped II only; epipodites on maxillipeds II and HI and on pereiopods I-IV. Type species Cryptopenaeus catherinae sp. nov. Etymology The generic name is derived from the prefix crypto, from the Greek kryptos meaning hidden, in combination with the generic name Penaeus, denoting the fact that this shrimp has been hidden from science until now; gender masculine. Taxonomic status and comments From the works of Bate (1881, 1888), Bouvier (1906), and Burkenroad (1936), it is clear that the generic complex forming the then accepted subfamily Solenocerinae presented many taxonomic difficulties. This subfamily consisted of three genera: Solenocera, shrimps with concave antennular flagella (Lucas 1849; Wood-Mason & Alcock 1891; Barnard 1950); Haliporus, shrimps with subcylindrical antennular flagella and movable lateral spines on the telson anterior to fixed pair (Bate 1881; Kensley 1968); and Hymenopenaeus, shrimps with subcylindrical antennular flagella and lacking lateral spines on the telson (Smith 1882; Wood-Mason & Alcock 1891; Barnard 1950). It is apparent from the literature, however, that Burkenroad (1936) was somewhat unhappy with the taxonomic status of Hymenopenaeus and went to the point of dividing the genus into four superspecies *. . . according to the presence or absence of branchiostegal or pterygostomian spines and to the nature of the postrostral armature’. Pérez Farfante (1977) revised the subfamily and, besides proposing that the subfamilies hitherto accepted should be elevated to the category of families of the superfamily Penaeoidea, divided Hymeno- penaeus into five genera partly based on the superspecific groups elaborated by Burkenroad (1936). In doing so Pérez Farfante takes into consideration the *. .. Shape of the antennular flagella and rostrum, proportions of the carapace, number and comparative size of the articles of the mandibular palp, presence or absence of certain carinae on the carapace, relative dimensions of the posterior A NEW GENUS AND SPECIES OF THE PENAEOID FAMILY SOLENOCERIDAE 125 two pairs of pereiopods, location of the distolateral spine of the lateral ramus of the uropod, structure of the petasma and degree of development of the arthrobranchia on somite VII’, as well as those characteristics originally used by Burkenroad. The system presented is very comprehensive and covers the previously known species extremely well. However, whereas the six specimens caught in southern Mozambique belong clearly to the family Solenoceridae and would have fitted into the genus Hymenopenaeus sensu lato, they do not belong to any of the five genera established by Pérez Farfante (1977), and have therefore been placed in a new genus, Cryptopenaeus. Table 1 sets out the similarities and differences between Cryptopenaeus and the other five genera, Hymenopenaeus, Haliporoides, Pleoticus, Hadropenaeus, and Mesopenaeus. The new genus is closely allied to Hymenopenaeus and Haliporoides but differs from the former in the arrangement of the rostral teeth, the absence of branchiostegal spines, the presence of a mid-dorsal carina on abdominal segments 2 and 3 and also by the short rostrum with a strongly convex ventral margin. Cryptopenaeus differs from Haliporoides in the arrange- ment of the rostral teeth, presence of a dorsal carina on the second abdominal segment, by the absence of a suprahepatic spine and by the short rostrum with a strongly convex ventral margin. The petasma of Cryptopenaeus differs from that of the other five genera in having the ventrolateral lobule entirely occupied by the ventral costa. Cryptopenaeus catherinae sp. nov. Fig. 1 Material Holotype: SAM-A16148 in the South African Museum, Cape Town, 3, 46,7 mm carapace length, caught off Cape Santa Maria in southern Mozam- bique (26°06’S 33°08’E) at a depth of 350 metres, on 16 December 1969. Alloptype: SAM-A16149 in the South African Museum, Cape Town, 2, 63,2 mm carapace length, caught off Monte Bello in southern Mozambique (25°00’S 35°21’E) at a depth of 500 metres, in September 1976. Paratypes: 4 gg, 44,5-47,7 mm carapace length, caught off southern Mozambique at a depth of 310 metres, in June 1973. One male paratype is in the National Museum of Natural History in Washington, D.C., and the remaining three will be sent to the British Museum (Natural History). Description Rostrum. Slightly downwardly directed, reaching to or just beyond end of first antennular segment; ventral margin convex; rostral teeth *4°; epigastric and three other teeth situated behind postorbital margin of carapace; adrostral carina short, just reaching postorbital margin; postrostral carina very well developed, long, almost reaching posterior margin of carapace and with conspicuous notch behind epigastric tooth; median groove absent. ANNALS OF THE SOUTH AFRICAN MUSEUM 126 XOAU09 X9AUO9 X9AU09 9ABDUOD 0} OSABDUOD 0} pue y10ySs A[3U011S A[3UO011S VY4sIeNg yysIeIs ‘Suo'T WYSIeNS WINjjsO1 JO UISIEU [RUSA, JUdSoI yuosqVv yuasq Vv JUOSIIg yuUdSo1g qudsald BUlIeS [eUISIeWUgng JuUdsog yuasqy yuosqy yuosqy JUISOIg qudsol ‘* BULIVS ORIPIeOOIyoURIg yuosqy yuosqyv yuosqy yuosq Vy JUdSo1g yuosqy ouids onedoyesdng quosqy quasoIg yuosqy yussold yuosq Vy quosqy ouids [eyIqiO yuasqe 10 JUISOI yuosqy yuosqy yuosqy JUISOI JudsoIg oulds uvIWUO}sOsA19}g yuasqe JO yussqy yuosqy quasolg JUISoIg quosqy yussold oulds yesojsorpsueig + ———}~ SaC 9st mS 9-€ 10 9-] wats 9-v BulTeS [eSIOp [BUIWIOpgYy S[PAIOJUL S[BAIOVUI S[PAIO}UI S[BAIOUL 4100} puz woly SuIseo1oOp SuIseaIoOp SUISeAIDOp SUISeOIDOp [eSO1 IST poyeredas 4199} [B.NSOI pure o1ysesidgq Ajrepnso1 Ajse[Ndo1 Aprepnsor Ajre[nsor WoOJJ poyeredas | 199} [e.ISOI 1S] Aq poyeredsg snapuadojdasy Aq poyeredag Snapuadosa=w BIDUIS Pd}e[91 ATISO]S SAY OY} WO] Aq poyeredag Aq poyeredag snapuadoi.poH SHINOAd oLsesidq pue oLysesidq saplosodyjoH snapuadouawld FL [ aTav.L ‘AOU ‘U3 Snapuadojdday BUIYSINSUNSIP SONslIajOeIeYD A NEW GENUS AND SPECIES OF THE PENAEOID FAMILY SOLENOCERIDAE 127 Carapace. Uniformly glabrous and lightly punctate; gastrofrontal and postocular grooves and horizontal suture absent; no supra-orbital spine; cervical sulcus and carina very well developed and long but not reaching dorsal midline; cervical carina terminating anteroventrally in prominent hepatic spine; gastro-orbital carina absent; postorbital spine prominent; antennal spine present but relatively small; antennal carina absent; orbito-antennal groove restricted to wide depression extending from below postorbital spine to below hepatic spine; hepatic carina sharp, anteroventrally directed and situated just anterior and below hepatic spine; hepatic sulcus wide and deep; extending posteriorly below hepatic spine; branchiocardiac carina distinct but not very sharp. Branchiostegal spine absent; pterygostomian spine prominent and sharp; submarginal carina long and sharp; no vertical suture or carina. Antennule. Flagella subequal in length; about 2,5 times length of antennular peduncle; subcylindrical; mesial flagella twice as thick as lateral flagella; prosartema flexible with pointed apex, reaching just beyond distal end of first antennular peduncle, copiously provided with long setae; stylocerite sharply pointed distally, straight and reaching just beyond end of eye or to end of first antennular article; distolateral spine prominent and long; parapenaeid spine absent. Scaphocerite. Distolateral spine reaching just beyond distal end of anten- nular peduncle; apex of lamella extending beyond distolateral spine; basicerite with single broad blunt tooth distally. Mandibular palp. Reaching to about basal one-third of carpocerite; proximal article 1,8 times as long as wide; distal article subequal to proximal, tapering to rounded apex. Maxilliped III. Endopodite not exhibiting sexual dimorphism; reaching distal end of scaphocerite; exopodite short, reaching less than half-way along merus of endopodites; epipodite present. Pereiopods. Exopodites present on all pereiopods, well developed, longest on first periopod and shortest on fifth; epipodites present on pereiopods I-IV; basipodites of first, second and third with prominent spines; ischial spine present on first pereiopod only; distinct coxal spine on fifth pereiopod. Pereiopod IV reaching to apex of mandibular palp; pereiopod V reaching to distal end of antennular peduncle. Extended laterally lengths of pereiopods in ascending order are: first, second and fourth, third and fifth. Abdomen. Uniformly glabrous; mid-dorsal carina present from posterior half of second segment to end of sixth where it terminates in short spine; short vertical groove on pleura of first segment; lateral carinae absent. Telson. Slightly longer than sixth segment; about as long as mesial ramus of uropod; median groove deep, occupying only anterior half of telson; apical spine somewhat blunt; pair of inconspicuous, very short, fixed subapical spines present; movable marginal spines lacking. Thelycum. Simple open structure; anterior portion formed by vertical posterior face of sternite between fourth pereiopods; posterior face with short 128 ANNALS OF THE SOUTH AFRICAN MUSEUM Fig. 1. Cryptopenaeus catherinae sp. noy. A. Lateral view, holotype 3 46,7 mm carapace length. B. Right prosartema. C. Telson. D. Left mandibular palp, ventral view. E. Left appendix masculina and interna, ventral view. F. Appendix masculina, dorsal view. G. Distal subquadrate process of right half of petasma. H. Petasma, ventral view. I. Thelycum. A NEW GENUS AND SPECIES OF THE PENAEOID FAMILY SOLENOCERIDAE 129 median groove and low lateral ridges; covered with short setae and obscured by coxal protuberances of fourth pereiopods. Posterior portion (between fifth pereiopods) consisting of elongate plate; broad central ridge occupying slightly more than anterior two-thirds of plate; well-defined lateral ridges extending from posterior sternal process to anterior margin of somite; two suboval, setose, boss-like structures present between anterior third of lateral ridges and median ridge; anterior margin of posterior sternal process interrupted by deep median sulcus. Petasma. Simple and very slightly involuted; dorsomedian lobule about two-fifths of total length of petasma; entirely united along midline; ventro- median lobule elongate and subtriangular; inner membranous section folded slightly on itself; heavily sclerotinized central ridge running length of lobule terminating distally in thick subquadrate process; distal margin smooth; proximolateral angle of quadrate process beak-like with four or five blunt teeth; ventral face of process concave; dorsal face convex; dorsolateral lobule elongate and subtriangular; apex situated under proximolateral angle of distal ventro- median process; lower inner angle forms small proximal process; ventral surface sparsely covered with long setae; ventral costa (occupying entire ventrolateral lobule) extending along lateral margin of petasma reaching half way into distal ventromedian process; apex free and bi-lobed; dorsal lobe longer than ventral lobe; ventral lobe with one to four minute teeth. Appendix masculina. Dorsally convex, ventrally concave, roughly trapezoid in shape; distal margin with row of short, stout setae; appendix interna subequal in length to appendix masculina, half fitting into concave face of latter; elongate with concave median surface; apex with short stout setae. Basal segment of endopodite of pleopod II as wide as long, its distolateral portion concave, subtriangular and produced into long, blunt spur. Colour in life. Body generally red, carapace with broad white stripe running from below hepatic sulcus to almost posterior margin of carapace on each side; this stripe wider in posterior half of carapace; on abdominal segments brighter ted patch running anteroventrally on each pleuron; distinct white longitudinal stripe on dorsal carina of abdominal segments 4-6; telson and uropods pinkish white becoming red along posterior edges; lateral margins of scaphocerite red; rostral crest and pereiopods pinkish white; basal segments of pleopods grey to white; pleopodal endopodites greyish white becoming bright red distally; marginal setae of pleura, pleopods and uropods orange while those of scapho- cerite and antennules white. Distribution Known only from the type locality. Ecological notes All the specimens were collected from the same general area, namely the Limpopo Bight in southern Mozambique. This is an important fishing ground 130 ANNALS OF THE SOUTH AFRICAN MUSEUM where the main species of interest are the spiny lobster, Palinurus delagoae, caught in about 280-350 metres, the langoustine, Nephrops andamanicus, trawled in 320-380 metres, and the pink or knife prawn, Haliporoides triarthrus, found in 300-500 metres. In this area, the continental slope is relatively gentle down to 500 metres after which it drops very steeply to about 3 000 metres. The substrate consists of muddy sand to sandy mud and the temperature at 300-500 metres depth recorded in April and September 1964 was 11-13°C (Instituto Hidrogrdafico Lisbon 1965, 1967). Although Cryptopenaeus catherinae has so far been found only in the type locality, it seems feasible to expect that, as its associate species, Haliporoides triarthrus, Aristeomorpha foliacea and Penaeopsis balssi are found off the coast of Natal, the distribution of C. catherinae could possibly extend southward as well. ACKNOWLEDGEMENTS I wish to thank the Fisheries Development Corporation and the South African Association for Marine Biological Research for their financial and administrative assistance; Dr Isabel Pérez Farfante of the Systematics Laboratory, National Marine Fisheries Service, Washington D.C., U.S.A., for having checked the identity of this species and for the meticulous way in which she read and criticized my manuscript; Professor A. E. F. Heydorn, Director of the Oceanographic Research Institute, Durban, for his encouragement and for his criticism of the manuscript; Dr P. F. Berry for reading and criticizing the paper; and finally my wife, after whom this species is named, for her encourage- ment, patience and understanding. REFERENCES BARNARD, K. H. 1950. Descriptive catalogue of South African decapod crustacea. Ann. S. Afr. Mus, 38: 1-837. Bate, C. S. 1881. On the Penaeidae. Ann. Mag. nat. Hist. (5) 8: 169-196. Bate, C. S. 1888. Report on the Crustacea Macrura collected by H.M.S. Challenger during the years 1873-1876. Rep. Sci. Results Voyage H.M.S. Challenger 1873-76, Zool. 24: 1-942. Bouvier, E. L. 1906. Observations sur les Peneides du genre Haliporus Bate. Bull. Mus. Oceanogr., Monaco 81: 1-10. BURKENROAD, M. D. 1936. The Aristaeinae, Solerocerinae, and pelagic Penaeinae of the Bingham Oceanographic Collection. Bull. Bingham Oceanogr. Coll. 5(2): 1-151. INsTITUTO HipROGRAFICO LISBON. 1965. Resultados das observagées oceanograficas no Canal de Mocambique, Cruzeiro AL 1/64: Abril-Maio 1964 1: 1-73. INstiruTO HiproGRAFIco LisBon. 1967. Resultados das observagées oceanograficas no Canal de Mocambique, Cruzeiro AL 2/64: Setembro-Outubro 1964 3: 1-107. KENSLEY, B. F. 1968. Deep sea decapod Crustacea from west of Cape Point, South Africa. Ann. S. Afr. Mus. 50: 283-323. Lucas, P. H. 1849. Genus Solenocera Lucas. Rev. Mag. Zool. (2) 1: 300. PEREZ FARFANTE, I. 1977. American solenocerid shrimps of the genera Hymenopenaeus, Se ee Pleoticus, Hadropenaeus new genus, and Mesopenaeus new genus. Fish. Bull. 75: 261-346. A NEW GENUS AND SPECIES OF THE PENAEOID FAMILY SOLENOCERIDAE ei SmiTH, S. I. 1882. Report on the results of dredging, under the supervision of Alexander Agassiz, on the East Coast of the United States, during the summer of 1880 by the U.S. Coast Survey Steamer ‘Blake’. 17: Report on the Crustacea, 1: Decapoda. Bull. Mus. comp. Zool., Harv. 10: 1-108. Woop-Mason, J. & AtcocKk, A. 1891. Natural history notes from H.M. Indian Marine Survey steamer ‘Investigator’, Commander R. F. Hoskyn, R.N., commanding. No 21. Note on the results of the last season’s deep-sea dredging. Ann. Mag. nat. Hist. (6) 8: 268-286. 6. SYSTEMATIC papers must conform to the /nternational code of zoological nomenclature (particularly Articles 22 and 51). Names of new taxa, combinations, synonyms, etc., when used for the first time, must be followed by the appropriate Latin (not English) abbreviation, e.g. gen. nov., sp. nov., comb. nov., syn. nov., etc. An author’s name when cited must follow the name of the taxon without intervening punctuation and not be abbreviated; if the year is added, a comma must separate author’s name and year. The author’s name (and date, if cited) must be placed’in parentheses if a species or subspecies is transferred from its original genus. The name of a subsequent user of a scientific name must be separated from the scientific name by a colon. Synonymy arrangement should be according to chronology of names, i.e. all published scientific names by which the species previously has been designated are listed in chronological order, with all references to that name following in chronological order, e.g.: Family Nuculanidae Nuculana (Lembulus) bicuspidata (Gould, 1845) Figs 14-15A Nucula (Leda) bicuspidata Gould, 1845: 37. Leda plicifera A. Adams, 1856: 50. Laeda bicuspidata Hanley, 1859: 118, pl. 228 (fig. 73). Sowerby, 1871: pl. 2 (fig. 8a—b). Nucula largillierti Philippi, 1861: 87. Leda bicuspidata: Nicklés, 1950: 163, fig. 301; 1955: 110. Barnard, 1964: 234, figs 8-9. Note punctuation in the above example: comma separates author’s name and year semicolon separates more than one reference by the same author full stop separates references by different authors figures of plates are enclosed in parentheses to distinguish them from text-figures dash, not comma, separates consecutive numbers Synonymy arrangement according to chronology of bibliographic references, whereby the year is placed in front of each entry, and the synonym repeated in full for each entry, is not acceptable. In describing new species, one specimen must be designated as the holotype; other speci- mens mentioned in the original description are to be designated paratypes; additional material not regarded as paratypes should be listed separately. The complete data (registration number, depository, description of specimen, locality, collector, date) of the holotype and paratypes must be recorded, e.g.: Holotype SAM-—A13535 in the South African Museum, Cape Town. Adult female from mid-tide region, King’s Beach Port Elizabeth (33°51’S 25°39’E), collected by A. Smith, 15 January 1973. Note standard form of writing South African Museum registration numbers and date. 7. SPECIAL HOUSE RULES Capital initial letters (a) The Figures, Maps and Tables of the paper when referred to in the text _ e.g. *... the Figure depicting C. namacolus ...’; *. .. in C. namacolus (Fig. 10)...’ (b) The prefixes of prefixed surnames in all languages, when used in the text, if not preceded by initials or full names e.g. DuToit but A.L.du Toit; Von Huene but F. von Huene (c) Scientific names, but not their vernacular derivatives e.g. Therocephalia, but therocephalian Punctuation should be loose, omitting all not strictly necessary Reference to the author should be expressed in the third person Roman numerals should be converted to arabic, except when forming part of the title of a book or article, such as “Revision of the Crustacea. Part VIII. The Amphipoda.’ ae Specific name must not stand alone, but be preceded by the generic name or its abbreviation to initial capital letter, provided the same generic name is used consecutively. ; Name of new genus or species is not to be included in the title: it should be included in the abstract, counter to Recommendation 23 of the Code, to meet the requirements of Biological Abstracts. NT ANTONIO J. DE FREITAS A NEW GENUS AND SPECIES OF THE PENAEOID FAMILY SOLENOCERIDAE (CRUSTACEA, DECAPODA) FROM SOUTH-EAST AFRICAN WATERS