STRUCTURE AND FORMATION OF THE BYSSUS COMPLEX IN MYTILUS (MOLLUSCA, BIVALVIA)

A review is presented of the mechanism of byssus productionin the genus Mytilus. The pedal glands which secrete the byssusmaterial are described, followed by an account of the morphology,structure and chemistry of the byssus itself. Finally, the releaseor shedding of the byssus from the pedal tissues is discussed. (Received 10 November 1981;     

DEMOGRAPHY AND GROWTH OF ANOMALOCARDIA BRASILIANA (GMELIN) (BIVALVIA: VENERIDAE) IN A MANGROVE, IN GUADELOUPE (FRENCH WEST INDIES)

Anomalocardia brasiliana is a venerid clam which lives slightlyburrowed in sandy mud of shallow water environments throughoutthe Caribbean region. A 42-month study in a mangrove lagoonshows that the population is characterised by a variable recruitmentpattern on a year-round basis but with infrequent success. TheGompertz function gives a good estimation of growth. The weight-sizerelationship shows alternative isometric and subdeterminantallometric growth periods. A short life and variable demographicstructure seem to be characteristics of lagoon as well as oftropical populations. (Received 5 February 1990; accepted 26 July 1990)     

THE OCCURRENCE OF ANOPAEA (BIVALVIA : INOCERAMIDAE) IN THE ANTARCTIC PENINSULA

The genus Anopaea represents a small but distinctive group ofinoceramid bivalves that apparently remained functionally endobyssate.The somewhat unusual morphology (for an inoceramid) probablyresults from structural modifications tofacilitate sedimentpenetration at a high angle and anchorage by an antero-ventralbyssus. Although never as common as thecontemporary genera Retroceramusand Inoceramus, Anopaea is now known from temperate bivalveassemblages in both the Northern and Southern Hemispheres. Itpersisted from the Late Jurassic (Tithonian) to the Early Cretaceous(Neocomian), and possibly even later. (Received 26 June 1980;     

SEXUAL DIMORPHISM OF SHELL SHAPE AND GROWTH OF VILLOSA VILLOSA (WRIGHT) AND ELLIPTIO ICTERINA (CONRAD) (BIVALVIA: UNIONIDAE)

Shell shape and growth of two unionacean species, Villosa villosaand Elliptio icterina, are analyzed with univariate and multivariatetechniques. The relationship of shape variables to size variablesis examined. Under the lognormal assumption, parametric testsof these allometric relationships are valid. Variables describingthe ventro-posterior region of the shell are shown to be thebest of those tested for discriminating between the sexes ofboth species regardless of statistical method. Neither speciesexhibits size sexual dimorphism. Shape sexual dimorphism ofV. villosa is constant during adult growth, but the more subtledimorphism of E. icterina changes as adults continue to grow. (Received 20 January 1986;     

EVOLUTION OF THE TELLINACEA (BIVALVIA)

The suspension feeding Astartacea appear to be among the earliestheterodonts. These organisms may have given rise to the Carditaceaand the rest of the heterodonts including the Tellinacea. Paleontological evidence indicates that the earliest Tellinaceawere suspension feeders with members that lived vertically ina burrow in shifting sand. These conditions resemble those foundin species of modern Donax in the Donacidae. From a Donax-likestate of suspension feeding evolution most likely proceededto non-selective feeders. Extant organisms that resemble thisstage are found in the Solecurtidae. A later stage resemblessome of the extant Psammobiidae. The final stage in tellinaceanevolution is the acquisition of deposit feeding with its associatedmorphology. These stages are observed in the Scrobiculariidae,Tellinidae and a few members of the Semelidae. (Received 27 April 1981;     

A NEW SPECIES OF LITHOPHAGA (BIVALVIA: LITHOPHAGINAE) BORING CORALS IN THE CARIBBEAN

A new species of Lithophaga is described as a small lithophaginemussel exclusively boring Madracis mir-abilis, M. decactis andM. formosa in Jamaica. The shell, musculature and pallial glandsshow modifications for live coral boring similar to those ofIndo-Pacific species of the genus. However, both the boringand posterior pallial glands are more primitive than other speciesexamined to date, interpreted as indicative of a more recentadaptation to life in a living coral habitat by this species. ^*Contribution No.359 of the Discovery Bay Marine Laboratory,University of the West Indies (Received 23 April 1985;     

REPRODUCTIVE CYCLE AND FECUNDITY OF THE DATE MUSSEL LITHOPHAGA LITHOPHAGA (BIVALVIA: MYTILIDAE)

The reproductive cycle and fecundity of the date mussel Lithophagalithophaga, L. a well-known, ediblespecies has been examined.Sexes are separate and the mean number of eggs per each gonadis 1.894 x 10⁶ ± 1.044 x 10⁶ S.D. Reproduction firstoccurs at an age of 2⁺years and at a shell length greater than0.9 cm. Gonad activity is annual and is observed at all ages.The sex ratio for individuals up to 7 cm is 3:1 in favour ofthe males, whereas it becomes 1:1 for individuals greater than7 cm. The release of gametes by males and females occurs almostsimultaneously and begins immediately after a decline in thehighest water temperature ( 27°C), an increase in salinity(>31) and a decrease in the dissolved oxygen (6.5 ppm). Smallpercentages of mature individuals appear during the first wintermonths thus lengthening the reproductive period. This phenomenonis attributed to the temperature difference in deeper waters,the delay in gamete release by young individuals, tide, waveaction and changes in salinity. The fecundity of Lithophagalithophaga is high because its life-cycle is adversely affectedby environmental factors such as waves and tides. Fecundityincreases with shell length, more so with total wet weight andmainly with the age of the animals. Summer seems to be the suitableseason to exploit the date mussel of shell lengths > 5 cm. (Received 6 September 1993; accepted 10 March 1994)     

FUNCTIONAL MORPHOLOGY AND FEEDING OF DONAX SERRA ROODING AND DONAX SORDIDUS HANLEY (BIVALVIA: DONACIDAE)

The functional morphology of Donax serra and D. sordidus fromSouth African beaches was examined, and comparative measurementsmade of the rate of water filtration. The two species differin the structure and ciliation of the ctenidia, the number andspacing of the ridges on the labial palps, the direction ofciliary currents on the surface of the mantle and visceral mass,and the length and coiling of the mid-gut. The maximum ratesof water filtration recorded showed similar relationships tosize for the two species, but in D. sordidus the rate declinedrapidly with time during the observations. These differencesindicate differences in feeding strategy related to differencesin distribution and behaviour of the two species on beaches.     

MORPHOLOGICAL BASIS OF EXCRETORY FUNCTION IN NAUSITORA FUSTICULA (JEFFREYS, 1860) (BIVALVIA: TEREDINIDAE)

The function of the excretory system of the teredinid bivalveNausitora fusticula is discussed on the basis of new informationon histology and ultrastructure. The wall of the auricles islined with podocytes that allow haemolymph ultrafiltration tothe pericardial cavity. These podocytes also show apical microvilliwith absorptive activity. The primary urine is drained fromthe pericardial cavity to the afferent ducts by a citiated bulb-likestructure. Theafferent and efferent ducts together form thekidney body. The afferent duct shows structures related to absorption,excretion and conduction of the urine. The efferent ducts, however,have structures concerned only with urine absorption and conduction. (Received 13 January 1997; accepted 15 July 1997)     

THE ANATOMY OF CALLOCARDIA HUNGERFORDI (BIVALVIA: VENERIDAE) AND THE ORIGIN OF ITS SHELL CAMOUFLAGE

Callocardia hungerfordi (Veneridae: Pitarinae) lives in subtidalmuds (220 to 240m C.D.) and is covered by a dense mat of mudthat, effectively, camouflages the shell. The periostracum is two layered. The inner layer is thick andpleated, the outer thin and perforated. From the outer surfaceof the inner layer develop numerous, delicate (0.5 mm in diameter),calcified, periostracal needles. These penetrate the outer periostracum.Mucus produced from sub-epithelial glands in the inner surfaceof the mantle, slides over the cuticle-covered epithelium ofthe inner and outer surfaces of the inner fold and the innersurface of the middle mantle fold to coat the outer surfaceof the periostracum and its calcified needles. Increased productionat some times produces solidified strands of mucus which bindmud and detrital material into their fabric to create the shellcamouflage. Calcified periostracal needles have been identified in othervenerids, including some members of the Pitarinae, but how theyare secreted and how the covering they attract is producedand, thus, how the whole structure functions, has not been explained. (Received 7 December 1998; accepted 5 February 1999)     

POPULATION GENETICS OF EUROPEAN ANODONTINAE (BIVALVIA: UNIONIDAE)

Enzyme electrophoresis was used to study population geneticsand molecular differentiation of European Anodontmae. The existenceof two genera (Anodonta Lamarck 1799 and Pseudanodonta Bour-guignat1876) is supported by the number of diagnostic loa (4) and Net'sD > 0.463 in all cases. In western and central Europe thereare two species of Anodonta, A. anatina (Linnaeus 1758) andA cygnea (Linnaeus 1758) while two other taxa of still uncertainrank were identified in the Mediterranean area. An estimatedmedium level of gene flow and pronounced genetic differentiationbetween-the taxa support this view. Data on genetic distancessuggest that the diversification of European Anodontinae tookplace in the middle-late Pleistocene (Received 15 August 1995; accepted 5 February 1996)     

BROODING AND NON-BROODING DACRYDIUM (BIVALVIA: MYTILIDAE): A REVIEW OF THE ATLANTIC SPECIES

The Atlantic species of the marine bivalve genus Dacrydium arereviewed, with particular emphasis on their hinge and protoconchcharacters. The basic groundplan of a Dacrydium comprises afunctional primary ligament, a paired series of primary teeth,and a posterior row of secondary teeth separated from the latterby a secondary ligament; this can be transformed into a singleseries either by loss of the secondary ligament and mergingprimary and secondary teeth, or by loss of secondary teeth andligament through paedomorphosis. Twelve species are recognized, of which eleven are illustrated.One abyssal species is not separable morphologically from theIndian Ocean D. speculum Poutiers, 1989 and is new to the Atlantic;four new species (D. wareni, D. dauvini, D. filiferum and D.balgimi) are described; a Caribbean form which is hardly distinctfrom the Eastern Pacific D. elegantu-lum Soot-Ryen, 1955, isdescribed as a new subspecies D. e. hendersoni. The larvae are brooded in D. hyalinum (Mon-terosato, 1875),D. viviparum Ockelmann, 1983 and D. balgimi. The brooding specieshave larger larvae (protoconch 210 to 315 µm long) thanthe non-brooding (protoconch 120 to 150 µm long), andreach a smaller adult size (1.4 to 3 mm instead of 4.5–5mm). A phylogenetic reconstruction is attempted using parsimonyanalysis of hinge and shell characters as well as the brooding/nonbrooding character. (Received 22 October 1996; accepted 28 November 1996)     

SOME BEHAVIOURAL AND ELECTRICAL RESPONSES OF SCROBICULARIA PLANA (BIVALVIA:TELLINACEA) TO SIPHONAL WOUNDING

Water pumping, valve movements and heart rate have been recordedfrom Scrobicularia for short periods of normal behaviour andthen after siphonal wounding. Scrobicularia exhibits regularand repetitive pumping periods interrupted for only 2–3s after siphonal wounding, without the regularity of these periodsbeing affected. Wounding does not prevent animals from usingtheir inhalant siphons for deposit feeding. A preliminary investigationof neural responses to stimulation has shown that wounding thesiphon causes minimal disturbance to the animal, a brief (2s)burst of nerve activity occurs, the siphon is retracted, butvalve adduction does not occur. In contrast to this tactilestimulation of the mantle edge always elicits a large burstof impulses in the posterior adductor nerve, valve closure results,usually for 14–15 s. ¹Present address: Dept of Zoology, University of Cape Town,Rondebosch 7700, South Africa. (Received 2 February 1981;     

THE ADDUCTOR AND RETRACTOR MUSCLES OF THE VELIGER OF PECTEN MAXIMUS (L.) (BIVALVIA)

In Pecten maximus (L.), retractor and adductor muscles becomefunctional in the early veliger larva. The twelve-day-old veligerhas four pairs of velar retractors, three pairs of retractorsattached to the posterior body wall and an anterior adductor.The pediveliger has in addition, pedal retractor muscles anda posterior adductor. The retractors consist of striated muscle:the adductors have both smooth and striated portions. The retractorsattach near the hinge, branch to a greater or lesser extent,then attach to specific areas of the velum, posterior body walland foot. Some features of the branching and of the dispositionof points of attachment form a pattern which exhibits mirrorsymmetry about the plane between the two shell valves. Thispattern is characteristic of the species. It is deduced thatretraction and protraction of the velum result from co-ordinatedsequences of muscle contractions. ^*Present address: Forest Products Research Centre, P.O. Box1358, Boroko, Papua New Guinea. (Received 15 June 1984;     

REPRODUCTION AND RECRUITMENT OF NUCULOMA TENUIS (BIVALVIA: NUCULOIDA) FROM LOCH ETIVE, SCOTLAND

A population of the protobranch bivalve Nuculoma tenuis at adepth of c. 54 m in Loch Etive, West Scotland, was sampled monthlyfrom September 1986 to October 1988. The density of N. tenuisin the samples, and the relative proportions of adults and postlarvae,varied markedly from month to month suggesting patchiness atthe scale of the sampling. There was evidence for spatial segregationof adults and postlarvae. A seasonal reproductive cycle occurred,with a synchronised spawnout in winter; the exact timing appearingto vary in successive years by up to 2 months. Despite markedlyseasonal spawning, no recruitment peak was evident in shell-lengthfrequencies, and benthic postlarvae were present throughoutthe year. This corroborates findings from an earlier laboratorystudy, suggesting a prolonged phase of meiobenthic developmentin this species. (Received 1 February 1995; accepted 15 March 1995)     

THE PALLIAL EYES OF CTENOIDES FLORIDANUS (BIVALVIA: LIMOIDEA)

The structure of the pallial eye in the Limidae has neverbeenelucidated properly, largely because they are difficultto see amongthe mass of surrounding mantle tentacles and becausethey are few,small, and lose their pigmentation when preserved.Possibly two eyetypes are present, simple cup-shaped receptorsin species of Lima,like those seen in the Arcoida, and morecomplex invaginated ones inCtenoides. The pallial eyes (;18on both lobes) of Ctenoidesfloridanus are formed by invaginationof the middle mantle fold at theperiostracal groove, so thatall its contained structures are derivedfrom the outer andlight is perceived through the inner epithelia ofthis fold.The eye comprises a simple multicellular lens and aphotoreceptiveepithelium beneath it of lightly pigmented cells andalternatingvacuolated, support cells. In some species of the Arcoidea, Limopsoidea and Pterioidea,pallialeyes occur on the outer mantle fold and thus beneath theperiostracum(and shell). The pallial eyes of Ctenoides floridanus andotherpterioideans, e.g. species of the Pectinidae, occur on themiddlefold and may thus have improved vision. In the Cardiodea,Tridacniidaeand Laternulidae (Anomalodesmata) pallial eyes occur ontheinner folds. There is thus a loose phylogenetic trend, in whichCtenoidesis a critical link, of increasing eye sophisticationcorrelatedwith the historical age of the clades possessing them. (Received 16 November 1999; accepted 20 January 2000)