A revision of Hesiospina (Psamathini,Hesionidae, Polychaeta)

Hesiospina Imajima and Hartman, 1964 Imajima, M and Hartman, O. 1964. The polychaetous annelids of Japan. Part 1. Allan Hancock Foundation Publications, Occasional Paper, 26: 1–166.  [Google Scholar] (Psamathini, Hesionidae, Polychaeta) is revised based on examination of all available types, other museum specimens and a large number of newly collected specimens from world-wide areas. Two species are recognized and redescribed, Hesiospina aurantiaca (Sars, 1862 Sars, M. 1862. Uddrag af en af detaillerade Afbildningar ledsaget udførlig Beskrivelse over følgende Norske Annelider. Forhandlinger i Videnskabsselskabet i Kristiania, 1862: 87–95.  [Google Scholar]), new combination, and H. vestimentifera Blake, 1985 Blake, J. A. 1985. Polychaeta from the vicinity of deep-sea geothermal vents in the eastern Pacific. I. Euphrosinidae, Phyllodocidae, Hesionidae, Nereididae, Glyceridae, Dorvilleidae, Orbiniidae, and Maldanidae. Bulletin of the Biological Society of Washington, 6: 67–101.  [Google Scholar]. The currently used name Hesiospina similis (Hessle, 1925 Hessle, C. 1925. Einiges über die Hesioniden und die Stellung der Gattung Ancistrosyllis. Arkiv för Zoologi, 17: 1–36.  [Google Scholar]) is treated as a junior synonym of both Hesiospina aurantiaca and Castalia longicornis Sars, 1862 Sars, M. 1862. Uddrag af en af detaillerade Afbildningar ledsaget udførlig Beskrivelse over følgende Norske Annelider. Forhandlinger i Videnskabsselskabet i Kristiania, 1862: 87–95.  [Google Scholar]. A lectotype is designated for H. aurantiaca, and the same specimen is used as neotype for C. longicornis, making the two objective synonyms. Hesiospina aurantiaca is widely distributed and recorded from the Caribbean, Gulf of Mexico, European Atlantic and Mediterranean waters, Japan, Papua New Guinea, the Great Barrier Reef, and New Caledonia, mainly from shallow waters, but down to over 500?m depth. Whereas there are some differences between populations from different regions, including distribution of uni- and bidentate chaetae, the different populations are not characterized by any obvious apomorphies and are treated as a single species. Hesiospina vestimentifera is associated with hydrothermal vents and is widely distributed in the east Pacific.     

Redescription of Valdivianemertes valdiviae (Bürger, 1909) (Nemertea: Hoplonemertea: Cratenemertidae) and designation of neotype

A century ago Bürger described the species Drepanophorus valdiviae from a single specimen taken from 155 m off the southern tip of Africa by the research vessel Valdivia during the German Deep Sea Expedition. Stiasny-Wijnhoff in 1923 Stiasny-Wijnhoff, G. 1923. On Brinkmann's system of the Nemertea Enopla and Siboganemertes weberi n. g. n. sp. Q J Microsc Sci., 67: 627–669.  [Google Scholar] transferred this species along with Amphiporus stannii (sensu Bürger 1895 Bürger, O. 1895. Die Nemertinen des Golfes von Neapel und der angrenzenden Meeres-Abschnitte. Fauna und Flora des Golfes von Neapel, 22: 1–743.  [Google Scholar]) to a new genus Valdivianemertes but did not mention a family affiliation. In 1993 Crandall transferred this genus to the family Cratenemertidae. During the Spanish Antarctic Expedition BENTART 2003, carried out on board the RV Hespérides, we found one specimen identified with certainty as Valdivianemertes valdiviae, at 602 m depth in the Bellingshausen Sea (Antarctica). As there is no extant holotype, we here redescribe this species from this new specimen and designate it the neotype of this species; photomicrographs of the different regions of the body and the proboscis structure are provided for the first time.     

Review of the genus Calamotropha Zeller (Lepidoptera: Crambidae: Crambinae) from China,with descriptions of four new species

Four new species of the genus Calamotropha Zeller are described from China: Calamotropha duofurcata sp. nov., Calamotropha abrupta sp. nov., Calamotropha aequilata sp. nov. and Calamotropha unispinea sp. nov. Three species are redescribed: Calamotropha formosella Bleszynski, 1961 Bleszynski, S. 1961. Revision of the World species of the Family Crambidae (Lepidoptera). Part I. Genus Calamotropha Zell. Acta Zool Cracov., 6(7): 137–272. pls. 20–71 [Google Scholar], Calamotropha josettae Bleszynski, 1961 Bleszynski, S. 1961. Revision of the World species of the Family Crambidae (Lepidoptera). Part I. Genus Calamotropha Zell. Acta Zool Cracov., 6(7): 137–272. pls. 20–71 [Google Scholar] and Calamotropha melli (Caradja and Meyrick, 1933 Caradja, A and Meyrick, E. 1933. Materialien zu einer Microlepidopteren-Fauna Kwangtungs. Dtsch entomol Z Iris., 47(3):123–144) [Google Scholar]). Calamotropha latella (Snellen, 1890 Snellen, PCT. 1890. A catalogue of the Pyralidina of Sikkim collected by Henry J. Elwes and the late Otto Möller, with notes by H. J. Elwes. Trans Entomol Soc Lond 1890:557–647, pls 19–20 [Google Scholar]) is newly recorded for China. Images of adults and illustrations of genitalia of the new species and the redescribed species are provided. A checklist and a key to the known Chinese species are presented, along with a map showing the distribution of these species.     

New records and hosts for three species of pseudionine bopyrids (Crustacea: Isopoda: Bopyridae) parasitizing munidid squat lobsters (Crustacea: Anomura: Munididae) in Philippine waters

Three species of pseudionine bopyrid isopods infesting four species of munidid squat lobsters are reported from Philippine waters: Pleurocryptella laevis (Richardson, 1910 Richardson, H. 1910. Marine isopods collected in the Philippines by the U. S. Fisheries steamer Albatross in 1907–8. Bureau of Fisheries Document., 736: 1–44.  [Google Scholar]) from Agononida analoga (Macpherson, 1993); Aporobopyrus retrorsa (Richardson, 1910 Richardson, H. 1910. Marine isopods collected in the Philippines by the U. S. Fisheries steamer Albatross in 1907–8. Bureau of Fisheries Document., 736: 1–44.  [Google Scholar]) from Munida philippinensis Macpherson and Baba, 1993 and Munida kuboi Yanagita, 1943; and Munidion laterale Richardson, 1910 Richardson, H. 1910. Marine isopods collected in the Philippines by the U. S. Fisheries steamer Albatross in 1907–8. Bureau of Fisheries Document., 736: 1–44.  [Google Scholar] from Paramunida scabra (Henderson, 1885). All of these hosts, except for Paramunida scabra, are recorded for the first time bearing parasitic isopods.     

Four new records and a new species of Dactylokepon Stebbing, 1910 (Epicaridea: Bopyridae: Ioninae) from Chinese waters

Five species of the parasitic isopod genus Dactylokepon are described from brachyuran crabs and a scyllarid shrimp collected in Chinese waters. Four species are first recorded from this region, D. richardsonae Stebbing, 1910 Stebbing, T. R. R. 1910. Isopod from the Indian Ocean and British East Africa.. Reports of the Percy Sladen Trust Expedition to the Indian Ocean in 1905, under the leadership of Mr. J. Stanley Gardiner, M. A. Transactions of the Linnean Society of London, Series 2, Zoology, 14(1): 83–122.  [Google Scholar] infesting Portunus argentatus (White), D. semipennatus Bourdon, 1983 Bourdon, R. 1983. Expédition Rumphius II (1975) Crustacés parasites, commensaux, etc. (Th. Monod éd.). VIII. Crustacés isopodes (3e partie: Épicarides Bopyridae).. Bulletin du Muséum National d'Histoire Naturelle, Paris, Série 4, 5(A3): 845–869.  [Google Scholar] infesting Portunus haanii (Stimpson) and Lupocyclus rotundatus Adams and White, D. holthuisi Bourdon, 1967 Bourdon, R. 1967. Sur deux nouveaux épicarides (Isopoda) parasites de crustacés decapods.. Zoologische Mededelingen, 42(17): 167–174.  [Google Scholar] infesting Eduarctus martensii (Pfeffer), and D. caribaeus Markham, 1975 Markham, J. C. 1975. New records of two species of parasitic isopods of the bopyrid subfamily Ioninae in the western Atlantic.. Crustaceana, 29(1): 55–67.  [Google Scholar] infesting Randallia trituberculata Sakai. In addition, one species is new to science, D. barbuladigitus n. sp. infesting Liagore rubromaculata (De Haan). Six brachyuran crabs are reported for the first time as hosts of bopyrids. The new species is distinguished from other species of Dactylokepon in having a prominent trifid frontal lamina and a distinct digitate barbula.     

Revision of the genus Mimopodabrus Wittmer (Coleoptera,Cantharidae)

The genus Mimopodabrus Wittmer is reviewed, and the genus diagnosis is re-described. Three new species are described, M. multidentatus sp. nov. (Guangdong, China), M. variabilis sp. nov. (Yunnan, China) and M. diversefoveolatus sp. nov. (Lao Cai, Vietnam), with illustrations of habitus, antennae and aedeagus. A species is transferred from Micropodabrus to this genus, M. bicoloriceps (Wittmer, 1989 Wittmer, W. 1989. 42. Beitrag zur Kenntnis der indo-malaiischen Cantharidae und Malachiidae (Coleoptera). Entomol Basil., 13: 209–237.  [Google Scholar]) comb. nov. A species is synonymized, M. bicoloriceps (Wittmer, 1989 Wittmer, W. 1989. 42. Beitrag zur Kenntnis der indo-malaiischen Cantharidae und Malachiidae (Coleoptera). Entomol Basil., 13: 209–237.  [Google Scholar]) comb. nov.?=?M. bicoloriceps Wittmer, 1997 syn. nov. and the definition of M. yunnanus (Wittmer, 1993 Wittmer, W. 1993. Zur Kenntnis der palaearktischen und indo-malaiischen Cantharidae (Coleoptera). Entomol Basil., 16: 203–253.  [Google Scholar]) is restricted. A key to all known species of this genus is provided.     

The freshwater shrimps of the genera Caridina and Parisia from karst caves of Sulawesi Selatan,Indonesia, with descriptions of three new species (Crustacea: Decapoda: Caridea: Atyidae)

The present study reports on collections of hypogean freshwater atyid shrimps of the genera Caridina Milne Edwards, 1837 Milne Edwards, H. 1837. Histoire naturalle des Crustacés, Comprenant l'Anatomie, la Physiologie et la Classification de ces Animaux, Vol. 2, 1–532. Paris (France): Libraire Encyclopedique de Roret.  [Google Scholar], and Parisia Holthuis, 1956 Holthuis, L. B. 1956. The troglobic Atyidae of Madagascar (Crudtacea, Decapoda, Natantia), Mem Inst Sci Madagascar ser.. A., 11: 97–110.  [Google Scholar], obtained from the karst caves and associated epigean waters of Sulawesi, Indonesia. Six species of Caridina were present, of which two are new to science and one is new to Sulawesi, as well as one new species of Parisia. Types of Caridina pareparensis De Man, 1892 De Man, J. G. 1892. Decapoden des Indischen Archipels.. Zool Ergebn Reise Niederland Ost‐Ind., 2: 265–527. pl. 15–29 [Google Scholar], and C. pareparensis parvidentata Roux, 1904 Roux, J. 1904. Décapodes d'eau douce de Cèlébes (Genres Caridina et Potamon).. Rev Suisse Zool., 12(3): 539–572. pl. 9 [Google Scholar], were re‐examined and redescribed; lectotypes for both taxa are designated. Caridina pareparensis parvidentata is here regarded as a distinct species. The new taxa are described, figured and compared with congeners.     

Rehabilitation of Bryconaethiops yseuxi Boulenger, 1899 (Characiformes: Alestidae) from the Congo River basin,Africa

Bryconaethiops yseuxi Boulenger, 1899 Boulenger, G. A. 1899. Matériaux pour la faune du Congo. Poissons nouveaux du Congo.. Annales du Musée du Congo, Tervuren, Zoologie 1(4: Polypères, Clupes, Mormyres, Characins), : 59–96.  [Google Scholar], originally described from “Haut Congo”, is rehabilitated. The species was synonymized, successively with B. microstoma (Günther, 1873 Günther, A. 1873. New fishes from Angola.. Annals and Magazine of Natural History, London (Series 4), 12(68): 142–144. [Taylor & Francis Online] , [Google Scholar]) and B. macrops Boulenger, 1920 Boulenger, G. A. 1920. Poissons recueillis au Congo belge par l'expédition du Dr. C. Christy.. Annales du Musée du Congo (Série 1), 2(4): 1–38.  [Google Scholar], subsequently rehabilitated, and then again considered as a junior synonym of B. microstoma. Bryconaethiops yseuxi is here considered as a valid species, easily distinguished from all other Bryconaethiops species by its small size (maximum: 72.2 mm SL), 7.5 rows of scales between the dorsal‐fin origin and the lateral line; 11–13/1/8–12 gill rakers on the first gill arch and long dorsal‐fin and anal‐fin bases, respectively, 15.7–17.6% of SL and 22.7–25.9% of SL.