REVIEW OF THE GENUS DENDRODORIS EHRENBERG, 1831 (GASTROPODA: NUDIBRANCHIA) IN THE ATLANTIC OCEAN

Six valid species of the nudibranch genus Dendrodons Ehrenberg,1831 inhabit the Atlantic Ocean, including the Mediterraneanand Caribbean Seas. Dendrodons lumbata (Cuvier, 1804), Dendrodonsgrandiflora (Rapp, 1827), Dendrodons nigra (Stimpson, 1855)(immigrant from the Red Sea), Dendrodons krebsu (Mörch,1863), Dendrodoru senegalensis Bouchet, 1975 and Dendrodonswarta Marcus & Gallagher, 1976. Additional data about thebiology and geographical distribution of these species are presented.New evidence suggests that other species assigned to the genusDendrodons, Dendrodons racemosa Pruvot-Fol, 1951 and Dendrodonsminima Pruvot-Fol, 1951, must be included in the genus DoriopsillaBergh, 1880. Three new species of Dendrodoris are describedfrom the Northeastern Atlantic and West Africa;Dendrodons angolensis,Dendrodoris guineana and Dendrodons herytra. The variable external morphology makes species recognition difficult.Instead, the diagnostic characters utilised to separate speciesare the shape of the male cirrus hooks, the structure of thereproductive system and features of the egg-mass. (Received 25 April 1995; accepted 1 August 1995)     

On the Brazilian species of halipegine genera (Trematoda: Derogenidae) from fishes,with new morphological data,hosts and synonyms

The genus Genarchella Travassos, Artigas & Pereira, 1928 is reinstated for some species from South American fishes previously attributed to Halipegus Looss, 1899. Aspects of the morphology of G. genarchella Travassos, Artigas & Pereira, 1928 and G. parva Travassos, Artigas & Pereira, 1928 are redescribed. Astyanax bimaculatus, Moenkhausia doceana, Oligosarcus robustus and Salminus maxillosus are recorded as new hosts of G. parva, and H. cryptorchis Mané-Garzon & Gascón, 1973 and H. szidati Yamaguti, 1971 [= G. tropica of Szidat (1954)] are listed amongst new synonyms of this species. Aspects of the morphology of Thometrema magnifica (Szidat, 1954) and T. overstreeti (Brooks, Mayes & Thorson, 1979) are redescribed. T. rioplatense Lunaschi, 1989 is considered a synonym of T. overstreeti. New host-records of T. overstreeti are Pimelodus maculatus and Rhamdia sp. G. genarchella of Hamann (1986) is considered as synonym of T. overstreeti. Paravitellotrema Watson, 1976, Caballeroiella Lamothe-Argumedo, 1977 and Quadripaludus Jimenez, Guajardo & Briseno, 1981 are considered synonyms of Genarchella. The features distinguishing Halipegus, Genarchella and Thometrema Amato, 1968 are discussed.     

Recent bivalve molluscs of the genus Calyptogena (Vesicomyidae)

The genus Calyptogena (Bivalvia: Vesicomyidae) comprises highlyspecialized bivalves living in symbiosis with sulphur-oxidizingbacteria in reducing habitats. In this study, the genus is revisedusing shell and anatomical features. The work is based on typematerial, as well as on the extensive collection of vesicomyidsobtained during twelve expeditions to the Pacific and IndianOceans. Nine Recent species are ascribed to the genus Calyptogena,four of which are new: C. pacifica Dall, 1891, C. fausta Okutani,Fujikura & Hashimoto, 1993, C. rectimargo Scarlato, 1981,C. valdiviae (Thiele & Jaeckel, 1931), C. gallardoi Sellanes& Krylova, 2005, C. goffrediae n. sp., C. starobogatovin. sp., C. makranensis n. sp. and C. costaricana n. sp. Thecharacteristic features of Calyptogena are: shell up to 90 mmin length, elongate-elliptical or elongate; presence of escutcheon;presence of broad posterior ramus (3b) of right subumbonal cardinaltooth as well as right posterior nymphal ridge; absence of pallialsinus as a result of attachment of intersiphonal septal retractorimmediately adjacent to ventral surface of posterior adductor;absence of processes on inner vulva of inhalant siphon; presenceof inner demibranch only, with descending and ascending lamellaewith interlamellar septa not divided into separate tubes. Themost closely related taxa to Calyptogena are probably the genusIsorropodon Sturany, 1896, and the group of species representedby ‘Calyptogena’ phaseoliformis Métivier,Okutani & Ohta, 1986. These groups have several charactersin common, namely absence of pallial sinus, presence of singleinner pair of demibranchs and absence of processes on innervulva of inhalant siphon. The worldwide distribution of thegenus Calyptogena suggests that methane seeps at continentalmargins are the major dispersal routes and that speciation waspromoted by geographical isolation. Recent species diversityand fossil records indicate that the genus originated in thePacific Ocean. Sufficient data to discuss the distribution atspecies level exist only for C. pacifica, which has a remarkablynarrow bathymetric range. Published studies on the physiologyof C. pacifica suggest that adaptation to a specific geochemicalenvironment has led to coexisting vesicomyid genera. The bacteria-containinggill of C. pacifica and other Calyptogena species is one ofthe most specialized in the family Vesicomyidae and may reflectthese ecological adaptations. (Received 23 December 2005; accepted 3 April 2006)     

FOUR NEW SPECIES OF TAMBJA BURN, 1962 (NUDIBRANCHIA: POLYCERIDAE) FROM THE INDO-PACIFIC

The genus Tambja previously included 24 described species. Fournew species, T. tentaculata n. sp., T. gabrielae n. sp., T.zulu n. sp. and Tambja victoriae n. sp., from the Indo-Pacificare described. Tambja tentaculata n. sp., from Guam, is theonly known species in the genus with well developed, dorsolaterallygrooved, oral tentacles. Its inner lateral teeth have a bifidinner cusp with two long, sharp denticles. The oral tentaclesof T. tentaculata are more typical of Roboastra species, whilethe shape of the inner lateral teeth is more typical of Tambja.Nevertheless, the arrangement of the two cusps of the innerlateral teeth and the presence of a rachidian tooth withoutdenticles and with a central notch at the anterior edge, typicalof the species of the genus Tambja, suggest the placement withinthis genus. Tambja gabrielae n. sp., from Indonesia and PapuaNew Guinea, has dark green to dark brown ground colour withbright yellow patches scattered on the body. Tambja zulu n.sp. from Durban, South Africa, is characterized by a black groundcolour with slender yellow longitudinal lines. Tambja victoriaen. sp. is a new species from Papua New Guinea and Australiathat has frequently been misidentified as Roboastra arika, characterizedby its blue body colour and yellow lines. The four species aredistinguishable based on differences in body coloration, ofcharacters of the radula and of the reproductive system. Anoverview on distinguishing features of all known Indo-PacificTambja species is presented. (Received 21 June 2004; accepted 20 January 2005)     

Exercise causes blood glutathione oxidation in chronic obstructive pulmonary disease: prevention by O2 therapy

Viña, José, Emilio Servera, Miguel Asensi, JuanSastre, Federico V. Pallardó, José A. Ferrero, JoséGarcía-de-la-Asunción, Vicente Antón, and JulioMarín. Exercise causes blood glutathione oxidation inchronic obstructive pulmonary disease: prevention by O₂therapy. J. Appl. Physiol. 81(5):2199-2202, 1996.The aim of the present study was to determinewhether glutathione oxidation occurs in chronic obstructive pulmonarydisease (COPD) patients who perform exercise and whether this could beprevented. Blood glutathione red-ox ratio [oxidized-to-reducedglutathione (GSSG/GSH)] was significantly increased when patientsperformed exercise for a short period of time until exhaustion. Theirresting blood GSSG/GSH was 0.039 ± 0.008 (SD)(n = 5), whereas after exercise itincreased to 0.085 ± 0.019, P < 0.01. Glutathione oxidation associated with exercise was partiallyprevented by oxygen therapy (resting value: 0.037 ± 0.014, n = 5; after exercise: 0.047 ± 0.016, n = 5, P < 0.01). We conclude that lightexercise causes an oxidation of glutathione in COPD patients, which canbe partially prevented by oxygen therapy.

     

PHYLOGENY OF THE GENUS ROSTANGA (NUDIBRANCHIA), WITH DESCRIPTIONS OF THREE NEW SPECIES FROM SOUTH AFRICA

Rostanga elandsia sp. nov., Rostanga aureamala sp. nov. andRostanga phepha sp. nov. are characterized by having the radulawith slender innermost lateral teeth, which lack denticles onthe inner side of the cusp and have a single denticle on theouter side. The outermost lateral teeth of these three speciesare elongate, but shorter than in other species of the genus.In addition, R. aureamala is the only species of the genus withrachidian teeth and R. phepha is unique within the genus Rostanga byvirtue of its white coloration with dark spots. A phylogenetic analysis shows that the three new species fromSouth Africa and Rostanga setidens (Odhner, 1939) are the sistergroup of the rest of the genus. The species from Japan and MarshallIslands (North Pacific Ocean) are basal in the sister cladecontaining the other species of Rostanga Bergh, 1879. The tropicalIndo-Pacific species of Rostanga are not monophyletic. The Atlanticand Eastern Pacific species form a monophyletic, derived clade,being the sister group of Rostanga australis Rudman & Avern,1989, which has a narrow range restricted to south eastern Australia.The widespread Indo-Pacific species Rostanga bifurcata Rudman& Avern, 1989, is the sister group of Rostanga dentacus Rudman& Avern, 1989, also widesprad in the tropical western Pacific. This phylogeny suggest s a viariant origin of the Sourth African, Atlantic-EasternPacific, and probably North Pacific species, whereas in thetropical Indo-Pacific most sister speceis are sympatric. (Received 16 May 1999; accepted 31 July 2000)     

REVISION OF THE GENUS NAPAEUS ALBERS, 1850 (GASTROPODA PULMONATA: ENIDAE). THE PROBLEM OF NAPAEUS (NAPAEINUS) NANODES (SHUTTLEWORTH, 1852) AND DESCRIPTION OF FIVE NEW SPECIES FROM ITS CONCHOLOGICAL GROUP

With this paper we initiate a taxonomic review of the genusNapaeus from the Canary Islands, indicating the statisticalmethodology used therein. We discuss the taxonomic problem ofNapaeus (Napaeinus) nanodes (Shuttleworth, 1852), designateits lectotype and describe five new species: Napaeus (Napaeinus)doliolum Henríquez, Napaeus (Napaeinus) bechi Alonso& Ibáñez, Napaeus (Napaeus) taguluchensisHenríquez, Napaeus (Napaeus) pygmaeus Ibáñez& Alonso and Napaeus (Napaeus) tagamichensis Henríquez,the first two from Tenerife; and the other three from La Gomera.Furthermore, we discuss the general relationships of the genusand its two sub-genera, whose original diagnoses are deficient;because of this, we think that in the future a broad reviewof the subfamily Eninae will be necessary in order to clarifythe actual position of this subfamily in the Canary Islands. (Received 11 March 1991; accepted 22 September 1992)     

Description de Syphabulea mascomai n. sp. et analyse du genre Syphabulea

Syphabulea mascomai n. sp., parasite de Sciurus vulgaris (L.) en Espagne, est décrite. S. mascomai se distingue des autres espèces du genre par: (i) la grande taille de ses oeufs; (ii) la taille relativement réduite de l'opercule de ces oeufs; (iii) par les particularités de l'ornementation du crochet accessoire au gubernaculum. La systématique et la répartition géographique des espèces du genre Syphabulea Gubanov, 1964 sont discutées. L'espèce type du genre est Syphabulea tjanschani (Ablasov, 1962) n. comb. [= Syphacia sp. d'Ablasov in Skrjabin et al. (1960); =Syphacia tjanschani Ablasov, 1962; =S. toschevi Petrov & Bayanov, 1962; =S. thompsoni sensu Li (1933); =S. thompsoni sensu Gubanov (1964); = Syphabulea sobolevi Gubanov, 1964]. Le genre Syphabulea n'était jusqu'ici connu que dans le région orientale, la région néarctique, et l'Est de la région paléarctique. La découverte d'un nouveau Syphabulea dans la péninsule ibérique, dont la faune parasitaire présente des caractères endémiques et relictuels, montre que la présence de ce genre dans la région paléarctique est probablement ancienne. Le genre Syphabulea est sympatrique du genre Rodentoxyuris Quentin & Tenora, 1975, lui aussi spécifique de Rongeurs Sciuroidea, dans une partie importante de la région holarctique. Syphabulea mascomai n. sp., parasitic in the caecum and large intestine of Sciurus vulgaris (L.) in Spain, is described. S. mascomai is characterised by: (i) its very large eggs; (ii) a shorter operculum on the eggs; and (iii) by the peculiar shape of the ornamentation of the accessory piece of gubernaculum. The systematics and the zoogeographical range of the genus Syphabulea Gubanov, 1964 are discussed. The type-species of the genus is: Syphabulea tjanschani (Ablasov, 1962) n. comb. [=Syphacia sp. of Ablasov in Skrjabin et al. (1960); =Syphacia tjanschani Ablasov, 1962; =S. toschevi Petrov & Bayanov, 1962, = S. thompsoni sensu Li (1933); =S. thompsoni sensu Gubanov (1964); =Syphabulea sobolevi Gubanov, 1964]. Until now the genus Syphabulea was known only from the Oriental region, from the Nearctic region and from the asiatic part of the Palearctic region. The discovery of a new species from Spain, an area in which the parasitological fauna exhibits endemic and relictual characteristics, indicates that this genus has probably been present in this part of Europe for quite a long time. The zoogeographical range of genus Syphabulea involves most of the Holarctic region, where it is sympatric with Rodentoxyuris Quentin & Tenora, 1975, another genus parasitic in the Sciuroidea.Se describe a Syphabulea mascomai n. sp. como parásito de Sciurus vulgaris (L.) en España. S. mascomai se distingue de las otras especies del género por: (i) el gran tamaño del los huevos; (ii) el tamaño, relavitamente reducido, del operculo de los huevos; (iii) las características de la ornemantación del gancho accesorio del gubernáculo. Se discute la sistemática y la repartición geográfica de las especies del género Syphabulea Gubanov, 1964. La especie tipo es: Syphabulea tjanschani (Ablasov, 1962) n. comb. [= Syphacia sp. del Ablasov in Skrjabin et al. (1960); =Syphacia tjanschani Ablasov, 1962; =S. toschevi Petrov & Bayanov, 1962; =S. thompsoni sensu Li (1933); =S. thompsoni sensu Gubanov (1964); = Syphabulea sobolevi Gubanov, 1964]. Hasta el presente se tenían datos del género Syphabulea en la Región Oriental, la Región Neártica y en el este de la Región Paleártica. El hallazgo de Syphabulea en la Península Ibérica, donde las parasitofaunas presentan características endémicas y relictuales, viene a sugerir que la presencia del género en la Región Paleártica es muy antigua. El género Syphabulea es simpátrico del género Rodentoxyuris Quentin & Tenora, 1975, tambien específico de Roedores Sciuroidea en la mayor parte de la Región Holártica.     

OSTEOPELTIDAE (MOLLUSCA:GASTROPODA): A NEW FAMILY OF LIMPETS ASSOCIATED WITH WHALE BONE IN THE DEEP-SEA

Osteopeltidae n. fam. is proposed for Osteopelta mirabilis n.gen. & sp., a limpet from whale skulls trawled on the ChathamRise and off the Chatham Islands, New Zealand. Osteopelta mirabiliscombines a pseudococculinid-like shell and radula with an add-isoniid-likeanimal. Apparent homologies in lepe-telloidean and cocculinoideanradulae are discussed. (Received 27 August 1986;     

NOTES ON THE OCCURRENCE OF MALES IN POPULATIONS OF POTAMOPYRGUS JENKINSI

Freshwater prosobranch snails of the genus Potamopyrgus arerenowned for being extremely variable and for reproducing parthenogenetically;in addition they are among the very few animals which appearto have successfully colonized Europe from the Antipodes (seeFretter & Graham, 1978, and Winterbourn, 1972 for reviewsand references). During investigations into the genetics and sex ratios of P.antipodum (or antipodarum) (Gray) in New Zealand, a period ofleave allowed some comparisons to be made with the AustralianP. nigra (Quoy & Gaimard), which is the subject of a separatenote (Wallace, 1978) and the European P. jenkinsi(Smith) discussedhere. (Received 10 March 1978;     

A phylogenetic analysis and systematic revision of the cryptobranch dorids (Mollusca, Nudibranchia, Anthobranchia)

The phylogenetic relationships of the cryptobranch dorids are studied based on morphological characters of species belonging to all previously described genera. The phylogenetic hypothesis supports the cryptobranch dorids as a monophyletic group. There are two major clades within the Cryptobranchia: the radula‐less dorids (Porostomata), and the radula‐bearing dorids ( Labiostomata new taxon ). Labiostomata consists of those taxa sharing a more recent common ancestor with Actinocyclus than with Mandelia, and includes several monophyletic groups: Actinocyclidae, Chromodorididae, Dorididae and Discodorididae. The traditional group Phanerobranchia is probably paraphyletic. The new classification proposed for the Cryptobranchia addresses concepts of phylogenetic nomenclature, but is in accordance with the rules of the International Code of Zoological Nomenclature. The following genera of cryptobranch dorids are regarded as valid: Doris Linnaeus, 1758, Asteronotus Ehrenberg, 1831, Atagema J. E. Gray, 1850, Jorunna Bergh, 1876, Discodoris Bergh, 1877, Platydoris Bergh, 1877, Thordisa Bergh, 1877, Diaulula Bergh, 1878, Aldisa Bergh, 1878, Rostanga Bergh, 1879, Aphelodoris Bergh, 1879, Halgerda Bergh, 1880, Peltodoris Bergh, 1880, Hoplodoris Bergh, 1880, Paradoris Bergh, 1884, Baptodoris Bergh, 1884, Geitodoris Bergh, 1891, Gargamella Bergh, 1894, Alloiodoris Bergh, 1904, Sclerodoris Eliot, 1904, Otinodoris White, 1948, Taringa Er. Marcus, 1955 , Sebadoris Er. Marcus & Ev. Marcus, 1960, Conualevia Collier & Farmer, 1964, Thorybopus Bouchet, 1977, Goslineria Valdés, 2001, Pharodoris Valdés, 2001, Nophodoris Valdés & Gosliner, 2001. Several genera previously considered as valid are here regarded as synonyms of other names: Doridigitata d’Orbigny, 1839, Doriopsis Pease, 1860, Staurodoris Bergh, 1878, Fracassa Bergh, 1878, Archidoris Bergh, 1878, Anoplodoris Fischer, 1883, Etidoris Ihering, 1886, Phialodoris Bergh, 1889, Montereina MacFarland, 1905, Ctenodoris Eliot, 1907, Carryodoris Vayssière, 1919, Austrodoris Odhner, 1926, Guyonia Risbec, 1928, Erythrodoris Pruvot‐Fol, 1933, Neodoris Baba, 1938, Siraius Er. Marcus, 1955, Tayuva Ev. Marcus & Er. Marcus, 1967, Nuvuca Ev. Marcus & Er. Marcus, 1967, Doriorbis Kay & Young, 1969, Pupsikus Er. Marcus & Ev. Marcus, 1970, Percunas Ev. Marcus, 1970, Verrillia Ortea & Ballesteros, 1981 . The genera Artachaea Bergh, 1882, Carminodoris Bergh, 1889 and Homoiodoris Bergh, 1882 have been poorly described and no type material is known to exist. They are regarded as incertae sedis until more material becomes available. The genus names Xenodoris Odhner in Franc, 1968 and Cryptodoris Ostergaard, 1950 are unavailable within the meaning of the Code. Hexabranchus Ehrenberg, 1831 is not a cryptobranch dorid, as suggested by other authors, because of the lack of a retractile gill. Other nomenclatural and taxonomic problems are discussed, and several type species, neotypes and lectotypes are selected. © 2002 The Linnean Society of London. Zoological Journal of the Linnean Society, 2002, 136 , 535?636.     

Shell characters and taxonomy of Latirus and related fasciolariid groups

The neogastropod family Fasciolariidae contains a complex ofgenera related to Latirus Montfort, 1810, many of which havetraits unusual for the family. In a taxonomic revision of someof these genera, based on shell characters, we restrict Latirusto a mainly Indo-West Pacific group of Pliocene to Recent species,which closely resemble the middle Miocene to Recent pantropicalgenus Hemipolygona Rovereto, 1899. Hemipolygona stenomphalus(Habe & Kosuge, 1966) is synonymized with H. recurvirostris(Schubert & Wagner, 1829). Lathyropsis Oostingh, 1939, basedon a small Pliocene species from Indonesia, is here tentativelysubsumed under Polygona Schumacher, 1817. The latter genus,ranging from the late Oligocene to Recent, occurs mainly inthe New World and eastern Atlantic, and contains at least twospecies groups centered on P. infundibulum Schumacher, 1817(type of genus) and P. angulatus (Röding, 1798). Taxa assignedby many authors to Latirulus Cossmann, 1889, are here reassignedto the new genus Turrilatirus (type species: Voluta turritaGmelin, 1791), from the Pliocene to Recent of the Indo-WestPacific. Latirulus is restricted to Eocene species. We assignvarious early Miocene to Recent species from the western Atlanticand eastern Pacific to the new genus Pustulatirus (type species:Latirus mediamericanus, Hertlein & Strong, 1951a). Taxaformerly assigned to Latirus but here removed from Fasciolariidaeinclude Latirus ewekoroensis Adegoke, 1977; the Eocene RusculaCasey, 1904; Lathyrus granifer and L. compactilis, both of Martin,1931; Latirus kirbyi Clark, 1938; Latirus tortilis var. nanafaliusHarris, 1899; and Latirus quercotillaensis Olsson, 1931. (Received 6 September 2005; accepted 29 May 2006)     

Eleven new Colobomatus species (Copepoda: Philichthyidae) from marine fishes

A survey of 79 fish species revealed 16 species of Colobomatus of which 11 are new and described below. The first ten new species were from Australian fish and the eleventh from a South African fish.The following species are described: Colobomatus cresseyi n. sp. from the eastern river garfish Hyporhamphus regularis ardelio (Whitley) and the snub-nosed garfish Arrhamphus sclerolepis krefftii (Stein-dachner); C. nanus n. sp. from the trumpeter Pelates quadrilineatus (Bloch); C. lesteri n. sp. from the common silver-belly Gerres ovatus (Günther); C. sewelli n. sp. from the seven-fingers tassel-fish Polynemus heptadactylus Cuvier; C. hispidus n. sp. from the blotched javelin-fish Pomadasys maculatus (Bloch); C. ornatus n. sp. from the whiptail Pentapodus setosus (Cuvier & Valenciennes); C. cribbi n. sp. from the barred-faced spine-cheek Scolopsis taeniopterus (Kuhl & van Hasselt); C. rothae n. sp. from the dusky flathead Platycephalus fuscus (Cuvier & Valenciennes) and the bar-tailed flathead P. indicus (L.); C. gietzelae n. sp. from the thread-fin silver-belly Gerres punctatus (Cuvier & Valenciennes); C. creeveyae n. sp. from the white trevally Pseudocarynx dentex (Bloch & Schneider); and C. mackayi n. sp. from an African haemulid, Pomadasys striatus (Gilchrist & Thompson). Colobomatus mylionus Fukui, 1965, is redescribed from the silver bream Acanthopagrus australis (Günther).Details of the mouthparts of C. kyphosus Sekerak, 1970, are given for the first time. This is a relatively plesiomorphic member of the genus (West, unpublished data), and its morphology assists in the interpretation of the appendages of the Australian species.Revised diagnoses for the family Philichthyidae Vogt and the genus Colobomatus hesse, 1873 are given. These incorporate the genus Colobomatoides Essafi & Raibaut, 1980 and the new Colobomatus species described herein respectively.     

THE SYSTEMATIC POSITION OF LAROCHEA FINLAY, 1927, AND INTRODUCTION OF A NEW GENUS AND TWO NEW SPECIES (GASTROPODA: SCISSURELLIDAE)

Species of the gastropod genus Larochea Finlay, 1927 are shownto be scissurellids without an anal shell slit or foramen. TheNew Zealand species, L. miranda Finlay, 1927 and L. secundaPowell, 1937, brood their young in the right subpallial cavityagainst a modified inner lip that is set well behind the aperturalplane. Larochea scitula n.sp. is based on shells from WanganellaBank, southern Norfolk Ridge. Larocheopsis n. gen. is introducedfor a minute species from off northern New Zealand that lacksa shell brood chamber. Larochea miranda and Larocheopsis amplexan.sp. are either gonochoristic with smaller males or consecutivehermaphrodites, while Larochea secunda and L. scitula are evidentlygonochoristic, having mature males and females of similar size. (Received 23 July 1992; accepted 10 December 1992)     

Taxonomic study of the genus Dichrogaster Doumerc (Hymenoptera: Ichneumonidae: Cryptinae) in Japan

Japanese species of the genus Dichrogaster are revised. Four species are recognized. Two species, D. imperialis n. sp. and D. parva n. sp., are described. Dichrogaster liostylus (Thomson) and D. kichijoi (Uchida) are redescribed. A key to the Japanese species is provided.     

The distribution of dinoflagellate cysts along the Galician (NW Spain) coast

We have studied the distribution of dinoflagellate cysts along10 Galician rías and part of their adjacent continentalshelf. Cyst abundance in the area averaged 856 cysts ml^–1,which is of the same order of magnitude as those found in otherareas of the western European coast. It was higher in the ríasthan in the shelf, having a very heterogeneous distribution,especially in the former. Cyst assemblages in these two areaswere different, suggesting that differences are due to cystproduction rather than to accumulation. Principal componentanalysis, cluster analysis, distribution of macroscopic characteristicsof cyst populations and distribution of single species suggestthat local factors control the distribution in the rías.Nevertheless, a general pattern that splits the whole area intotwo-to the north and to the south of the ría de Camariñas-canbe distinguished. This latter trend was also observed in theshelf and, in our opinion, It should be attributed to threeconcurrent causes: the effect of different upwelling intensitiesor frequencies, the effect of the different numbers and sizesof the ría in each area, and the effect of the presenceof different water masses in these areas. The cyst distributionof a number of individual species was examined and showed threegeneral groups: species with very restricted distribution, suchas Alexandrium sp2 or Scrippsiella sp4, species with a widespreaddistribution along the rías, such as several Scrippsiellaspecies, and species mainly distributed along the shelf, suchas Gymnodinium catenatum. The distribution of cysts belongingto red tide organisms fits quite well with that of their correspondingmotile phases dunng the three previous years for most of theorganisms studied and also during the 1992–1993 period(7–8 years later), but the role of this resting stagein initiating such blooms seems to be highly variable with species.