Systematics and phylogeny of the caryophyllidia-bearing dorids (Mollusca, Nudibranchia), with descriptions of a new genus and four new species from Indo-Pacific deep waters

The phylogenetic relationships of the caryophyllidia-bearing dorids are studied, based on the examination of the type species of all the genera previously described. The phylogenetic hypothesis supports that the caryophyllidia-bearing dorids are a monophyletic group and the sister group of the clade formed by Astemnotus Ehrenberg, 1831 and Halgerda Bergh, 1880. Several genera previously considered as valid or regarded as uncertain are here synonymized: Peronodoris Bergh, 1904, Trippa Bergh, 1877, Phlegmodoris Bergh, 1878, Petelodoris Bergh, 1881, Kentrodoris Bergh, 1876, Audura Bergh, 1878, Centrodoris P. Fischer, 1883, Anisodoris Bergh, 1898, Awuka Er. Marcus, 1955, Rhabdochiia P. Fischer, 1883, Boreodoris Odhner, 1939, Dictyodoris Bergh, 1880, Gravieria Vayssiere, 1912, Aporodoris Ihering, 1886. The following genera are regarded as valid: Astemnotus, Atagema J.E. Gray, 1850, Jorunna Bergh, 1876, Platydoris Bergh, 1877, Diaulula Bergh, 1878, Rostanga Bergh, 1879, Halgerda Bergh, 1880, Baptodoris Bergh, 1884, Gargamella Bergh, 1894, Alloiodoris Bergh, 1904, Sclerodoris Eliot, 1904, Taringa Er. Marcus, 1955, Thorybopus Bouchet, 1977. The new genus Nophodoris is described based on two new species from New Caledonia deep waters. Two additional new species from New Caledonia belonging to the genera Atagema and Gargamella are also described. Nomenclatural and taxonomic problems are discussed, and several type species, neotypes and lectotypes are selected.     

The phylogeny of Halgerda (Opisthobranchia, Nudibranchia) with the description of a new species from Okinawa

This paper proposes a refined hypothesis of evolution for the tropical Indo-Pacific nudibranch genus Halgerda . Numerous specimens from 31 species were examined anatomically and literature from four additional species was reviewed, bringing to 33 the ingroup taxa. Fifty-three characters were considered from these examinations. The outgroup Asteronotus was used to polarize the characters. The phylogeny obtained from the analysis of the characters supports the hypothesis that Halgerda is a monophyletic group. A species previously placed with the genus Sclerodoris is examined and determined to be a member of the genus Halgerda . Phylogenetic analysis places this species, H. paliensis , as a basal member of the genus . Halgerda paliensis appears to be restricted to the Hawaiian Islands. Specimens previously identified as Sclerodoris paliensis from the Marshall Islands actually represent H. dalanghita Fahey & Gosliner, 1999. A new species, Halgerda onna , is described and presented as the sister taxon to a basal member of the genus. A range and depth extension of a previously described species, H. malesso , is presented. The present phylogeny is then compared to previous studies, in particular those of Fahey & Gosliner (1999a,b) .     

On some species of Chelidonura (Opisthobranchia:Aglajidae) from Zanzibar and Fiji

The anatomy of specimens of Chelidonura philinopsis Eliot, 1903 and a new species of Chelidonura collected in Zanzibar, are described. Preserved specimens of Chelidonura, from Fiji, most probably C. varians Eliot, 1903 (=C. velutina Bergh, 1905) are discussed. Chelidonura philinopsis is compared with C. hirundinina {Quoy & Gaimard, 183 2) and it is suggested that at this stage they should remain as distinct species. C. punctata Eliot, 1903, the other species of the genus recorded from Zanzibar, is compared with two similarly coloured species from Japan, C. fulvipunctata, Baba, 1938 and C. tsurugensis, Baba & Abe, 1959.
The species suggest that the structure of the alimentary canal and the reproductive system (excluding the penis) are constant within the genus.     

The taxonomy and biology of further aeolidacean and arminacean nudibranch molluscs with symbiotic zooxanthellae

The occurrence of symbiotic zooxanthellae in further aeolid and arminacean nudibranch molluscs is described for the first time. The aeolid Aeolidiopsis ransoni Pruvot-Fol is redescribed, and a new species of Aeolidiopsis , also feeding on the colonial zoantharian Palythoa , is described. Both have symbiotic zooxanthellae. The taxonomy of the family Aeolidiidae is discussed and the genus Berghia Trinchese, 1877 is considered a synonym of Spurilla Bergh, 1864. Spurilla major (Eliot, 1903) and a new species of Spurilla are reported to have zooxanthellae while another new species of Spurilla is without zooxanthellae. The glaucid aeolid Pteraeolidia ianthina (Angas) is shown to have symbiotic zooxanthellae, as is the arminacean Doridomorpha gardineri Eliot, which is reported to feed on the alcyonarian blue coral, Heliopora. In all cases, the morphological adaptations developed for this symbiosis are described. Further notes on the Porites-fetding arminacean Pinufius rebus Marcus & Marcus and the aeolid Phestilla lugubris (Bergh) are included and a facultative symbiosis with zooxanthellae is suggested for the latter. The tion of symbiosis with zooxanthellae within nudibranchs is discussed and it is suggested that the relationship has evolved independently on several occasions.     

The morphology and taxonomy of the Antarctic species of Tritonia Cuvier, 1797 (Nudibranchia: Dendronotoidea)

The external morphology and anatomy of the Antarctic nudibranchs Tritonia vorax Odhner, 1926, and Tritonia antarctica Pfeffer in Martens & Pfeffer, 1886, is redescribed in detail and compared with other nominal tritoniids from the Antarctic and Subantarctic waters. Tritonia appendiculata Eliot, 1905, T. challengeriana Eliot, 1907a, non Bergh, 1884, T. chalkngeriana Odhner 1926, non Bergh, 1884, and Marionia cmullata Vicente & Arnaud 1974, non (Couthouy, in Gould 1852), are shown to be synonymous with T. antarctica. Only Tritonia antarctica is a true High Antarctic species, with a distribution around the continental shelf, Antarctic Peninsula and South Georgia. T. vorax is confined to South Georgia and Subantarctic waters.     

The anatomy and biology of alcyonarian-feeding aeolid opisthobranch molluscs and their development of symbiosis with zooxanthellae

The anatomy of seven species of aeolid opisthobranch molluscs is described. They are all considered to be specialized feeders on alcyonarian coelenterates and to belong to one genus Phyllodesmium (Glaucidae; Favorininae). Two species are considered to be new. Favorinus horridus Macnae, Aeolidia poindimiei Risbec, Cratena macphersonae Burn and another species not studied in this paper, Hervia serrata Baba, are transferred to Phyllodesmium from the genera in which they are currently placed. Myrrhine Bergh, Babaiella Risso-Dominguez and Phyllodesmiopsis Risso-Dominguez are considered synonyms of Phyllodesmium. The two new species feed on Xenia and P. poindimiei feeds on Telesto. It is shown that the species of Phyllodesmium exhibit an evolutionary series in the development of symbiosis with zooxanthellae. The zooxanthellae are obtained from the alcyonarians upon which the aeolids feed. Morphological peculiarities present in some members of the genus are considered to be associated with the symbiosis.     

Ateleaspis tessellata Traquair, a non-cornuate cephalaspid from the Upper Silurian of Scotland

Ateleaspis tessellata Traquair, a non-cornuate cephalaspid from the U. Silurian of Scotland, is re-examined on the evidence of new material from the original localities. The species is found to be less 'primitive' than was previously thought in that the pectoral fins are separated from the trunk posteriorly by a distinct sinus and the two dorsal fins are developed essentially as in Aceraspis robustus Kiaer. The ventral visceral exoskeleton is described for the first time. Ateleaspis and Aceraspis are so close in so many respects that retention of separate genera is unnecessary; Aceraspis must be suppressed since Ateleaspis has priority. Revised diagnoses of the genus Ateleaspis and its two species, A. tessellata Traquair and A. robustus (Kiaer), are given and their relationships with other non-cornuate cephalaspids discussed.     

Adaptive evolution of bindin in the genus Heliocidaris is correlated with the shift to direct development

Abstract Sea urchins are widely used to study both fertilization and development. In this study we combine the two fields to examine the evolution of reproductive isolation in the genus Heliocidaris . Heliocidaris tuberculata develops indirectly via a feeding larva, whereas the only other species in the genus, H. erythrogramma , has evolved direct development through a nonfeeding larva. We estimated the time of divergence between H. erythrogramma and H. tuberculata from mitochondrial DNA divergence, quantified levels of gametic compatibility between the two species in cross-fertilization assays, and examined the mode of evolution of the sperm protein bindin by sequencing multiple alleles of the two species. Bindin is the major component of the sea urchin sperm acrosomal vesicle, and is involved in sperm-egg attachment and fusion. Based on our analyses, we conclude that: the two species of Heliocidaris diverged less than five million years ago, indicating that direct development can evolve rapidly in sea urchins; since their divergence, the two species have become gametically incompatible; Heliocidaris bindin has evolved under positive selection; and this positive selection is concentrated on the branch leading to H. erythrogramma . Three hypotheses can explain the observed pattern of selection on bindin: (1) it is a correlated response to the evolution of direct development in H. erythrogramma; (2) it is the result of an intraspecific process acting in H. erythrogramma but not in H. tuberculata; or (3) it is the product of reinforcement on the species that invests more energy into each egg to avoid hybridization.     

Species of the genus Crotonia (Acari: Cryptostigmata) from New Zealand

Five new species of Crotonia from New Zealand ( C. cervicorna, C. cupulata, C. longibulbula, C. tuberculata and C. reticulata ) are described as new, and two species ( C. cophinana (Michael 1908) and C. caudatis (Hammer 1966)) are redescribed. Five species groups of the genus are characterized and a key to the adequately described species of the world is presented.     

Sperm ultrastructure in the nudibranch genus Halgerda with reference to other Discodorididae and to Chromodorididae (Mollusca: Opisthobranchia)

Comparative sperm ultrastructure within the molluscan nudibranch genus Halgerda (Discodorididae) was examined for the first time using transmission electron microscopy (TEM), based on 17 of the 35 known species. In addition, observations on two other discodorids are made to facilitate outgroup comparison with Halgerda, including one species of Discodoris (D. boholiensis) and Asteronotus cespitosus (currently accepted as the closest sister taxon to Halgerda). Comparison was also made with some genera of the Chromodorididae in view of sperm similarities. Spermatozoa of all species examined were of the complex, helical, elongate ( approximately 300-400 micro m) type characteristic of most heterobranch gastropods. These cells exhibit the following discrete regions (in anteroposterior sequence) : an acrosomal complex (composed of a rounded, membrane-bound vesicle and a column-like pedestal); a solid, helical nucleus; an elongate, helical midpiece (composed of an axoneme and associated nine coarse fibers, an enveloping mitochondrial derivative of matrix, and paracrystalline materials and glycogen helix); an annular complex; and a short glycogen piece. Of these regions, the midpiece is by far the longest, occupying over 90% of the total sperm length. Comparison with other members of the radula-bearing cryptobranch dorids reveals several sperm similarities to other genera in the clade, particularly those of other Discodorididae and also with the Chromodorididae. Comparison with previously studied genera reveals noteworthy sperm differences within the Discodorididae. The most notable differences are the internal structure of the acrosomal pedestal (long and homogeneous in Halgerda, Discodoris; short and homogeneous in Asteronotus; long and finely striated in Rostanga; oblong with angular electron-lucent striations in Jorunna) and the internal structure of the glycogen piece. The pronounced helical keels of most Halgerda and Discodoris nuclei contrast with the weakly helical nucleus of Asteronotus. Sperm features alone do not provide a means of defining the genus Halgerda or the family Discodorididae nor do they support the monophyletic status of the caryophyllidia-bearing dorids. Important sperm characters such as the acrosome, nucleus, and midpiece can often still be determined from specimens that have been initially fixed in formalin, then stored in ethanol for extended periods of time (i.e., museum material). Of all sperm features, the mitochondrial derivative of the midpiece is the most resistant to long-term fixation : the survival of acrosomal, nuclear, and axonemal components is variable, presumably a factor of prefixation autolysis, varied primary fixation times and temperatures, formalin quality, and duration of alcohol storage.     

我国几种新记录的硅藻

本文报道了采自安徽的我国分布新记录的硅藻有3种及3变种。     

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.     

A cladistic analysis of Scinax (Anura: Hylidae)

The hylid frog genus Scinax ranges from southern Mexico to eastern Argentina. The 84 recognized species are currently arranged in five groups: the Scinax rubra , Scinax rostrata , Scinax catharinae , Scinax staufferi , and Scinax perpusilla species groups. Although a few species groups are distinctive, compelling evidence of monophyly is lacking for three groups, and their interrelationships remain virtually unknown. With the objective of testing the monophyly of the species groups and exploring their interrelationships, a cladistic analysis was performed, employing 86 characters from osteology, myology, adult and larval external morphology, reproductive biology, and karyotypes taken from 36 representative species of the five species groups plus eight outgroup taxa. The analysis of the resulting data matrix shows moderately well-supported (as assessed through Bremer support and parsimony jackknifing) S. catharinae and S. rostrata species groups. The S. staufferi species group is polyphyletic, as currently composed, given that some of its species are nested within the S. catharinae species group. The only representative of the S. perpusilla species group is the sister species of the S. catharinae species group. Although weakly supported, the representatives of the S. rostrata and S. staufferi species groups are nested, separately, within the S. rubra species group. In order to have a taxonomy consistent with these results, it is proposed not to recognize the S. rubra group but to recognize a more inclusive rubra clade that includes all studied exemplars of the former S. rubra group, plus some of the S. staufferi group and all of the S. rostrata group. Similarly, a catharinae clade is recognized, within which all studied exemplars of the S. catharina e group (that now includes Scinax berthae and Scinax agilis ) and the one studied representative of the S. perpusilla group are included.     

Die Gattung Bathydoris Bergh, 1884 (Gnathodoridacea) im phylogenetischen System der Nudibranchia (Opisthobranchia, Gastropoda)

The genus Bathydoris Bergh, 1884 (Gnathodoridacea) in the phylogenetic system of the Nudibranchia (Opisthobranchiu, Gastropoda) The position of the genus Bathydoris Bergh, 1884 in the phylogenetic system of the Nudibranchia is discussed. Doridoxa Bergh, 1900, a genus which is assigned to the taxon Gnathodoridacea together with the genus Bathydoris, is taken out from this taxon, lacking snapomorphies. Doridoxa is considered to be a sister grou of the Euctenidiacea, with the transrormation of the right digestive gland into a caecum as the only synaomorphy with the latter. The Gnathodoridacea with the one enus Bathydoris is removed from the taxon Doridacea and considered to be the sister group or the latter. Gnathodoridacea and Doridacea form the taxon Euctenidiacea with the synapomorphy “dorsomedial position of anus and nephroproct”.     

Tazonomy of Toxoplasma.

After reviewing reports of the hosts, structure and life cycle of Toxoplasma, the genus is placed in the apicomplexan family Eimeriidae and the folllowing 7 species are recognized: Toxoplasma gondii (Nicolle & Manceaux) (type species) from about 200 species of mammals and birds, with oocysts in felids; Toxoplasma alencari (Da Costa & Pereira) from the frog Leptodactylus ocellatus; Toxoplasma brumpti Coutelen from the iguana Iguana tuberculata; Toxoplasma colubri Tibaldi from the snakes Coluber melanoleucus and Coluber viridiflavus; Toxoplasma hammondi (Frenkel & Dubey) (a new combination for Hammondia hammondi) from the house mouse with oocysts in the domestic cat; Toxoplasma ranae Levine & Nye from the leopard frog Rana Pipiens; and Toxoplasma serpai Scorza, Dagert & Iturriza Arocha from the toad Bufo marinus.     

Opisthobranchiate Mollusca from Tanzania (Suborder:Doridacea)

Twenty-two species of Doridacea are described from the vicinity of Dar es Salaam, Tanzania. None is new to science, but one species of the genus Gymnodoris was too immature to be fully identified. Ten of the 22 species are known from the Hawaiian Islands, indicating that many species of dorid occur throughout the Indian Ocean and the Pacific as far as Hawaii. One species (Jorunna tomentosa) appears to be cosmopolitan, and two may possibly be confined to the coast of Africa (Chromodoris annulata and C. vicind).
Sixty-nine species of dorid have already been reported from Tanzania by Eliot. Nine species in the present collection were not found by him, so 78 are now known from the area.