A review of flying fishes of the subgenus Hirundichthys (genus Hirundichthys, exocoetidae). 1. Oceanic species: H. speculiger, H. indicus sp. nova

A systematic revision of flying fishes of the subgenus Hirundichthys s.str was carried out based on a study of meristic and morphometric traits and characteristics of pigmentation of fishes from the local populations of species belonging to the subgenus. It is found out that the subgenus includes four species: oceanic H. speculiger from the Atlantic, Pacific and Indian Oceans, oceanic H. indicus sp.n. from the waters of the Indian Ocean, nerito-oceanic H. oxycephalus from the waters of the Indo-West Pacific and nerito-oceanic H. affinis from the Atlantic Ocean. The first part of the review focuses on two oceanic species with a large “mirror” on the pectoral fins: H. speculiger and H. indicus. A comparison of local populations showed that the species H. indicus is polytypic and consists of two subspecies. One of the subspecies—nominative H. indicus indicus—is distributed in the western and the central parts of the Indian Ocean and the other—H. indicus orientalis ssp.n.—in the Eastern Indian Ocean. Maps showing a geographical distribution of the species and the subspecies in the World Ocean are drawn up.     

The fisheries biology of flying fishes (Families: Exocoetidae and Hemiramphidae) from the Camotes Sea, Central Philippines

The catches of a small artisanal fishery for flying fishes (Families Exocoetidae and Hemiramphidae) on the Danajon Bank in the Camotes Sea. Central Visayas, were recorded during a 14-month period between 1987–1988. Catches were made using floating drive-in-nets deployed from small motorized canoes. Three species, Cheilopogon nigricans, Cypselurus opisthopus and Oxyporhamphus convexus , formed about 90% of landings. Growth, mortality and related parameters for the three dominant species in the catch were estimated from length-frequency data. Seasonal variations in catch rate and recruitment are described and thought to be linked to the two monsoon periods in the Philippines. Total mortality rates were very high and, while these may be the result of migratory movements rather than attrition, they are a cause for concern in such a highly selective fishery.     

Skull structure of the flying fish Cheilopogon pinnatibarbatus (Beloniformes, Exocoetidae)

The skull of the flying fish Cheilopogon pinnatibarbatus is first described in comparison with literature data on other four-winged flying fishes (subfamily Cypselurinae). The skull of Ch. pinnatibarbatus is characterized by the following features: (1) a multitude (about 40) of minute pores in the canal of the lateral line of the nasale; (2) a big opening in the roof of the myodome; (3) the lateral line canal of dentale by far does not reach the symphysis; (4) the tip of praeoperculum does not reach the upper edge of the hyomandibulare; (5) the posterior part of the angulare is weakly covered by the articulare and almost reaches from the outside the joint for articulation with the quadratum. Ppublished in Voprosy Ikhtiologii, 2007, Vol. 47, No. 3, pp. 284–291. This article was submitted by the authors in English.     

Phylogenetic studies of the subgenus Nialoe (s. lat.) (Coleoptera, Carabidae, Genus Pterostichus), part 2: The Asymmetricus species group

Pterostichus (Nialoe) asymmetricus Bates and its allies are revised based on the membranous parts of their genitalia. Four new taxa, P. (N.) ovaliphallus sp. nov., P. (N.) fujimurai ibukiyamanus ssp. nov., P. (N.) shotaroi kiimontanus ssp. nov., and P. (N.) basilobatus sp. nov. are described. A cladistic analysis based on 31 morphological characters reveals that Daisenilaoe (s. str.) Nakane and Straneo is included as one clade within Nialoe (s. str.). The speciation and dispersal process of this species group are also discussed.     

Antarctic icefishes (Channichthyidae): a unique family of fishes. A review, Part II

Icefish or white- blooded fish are a family of species unique among vertebrates in that they possess no haemoglobin. With the exception of one species which occurs on the southern Patagonian shelf, icefish live only in the cold-stable and oxygen-rich environment of the Southern Ocean. It is still questionable how old icefish are in evolutionary terms: they may not be older than 6 Ma, i.e. they evolved well after the Southern Ocean started to cool down or they are 15–20 Ma old and started to evolve some time after the formation of the Antarctic Circumpolar Current. Individuals of most icefish species with the exception of species of the genus Champsocephalus have been found down to 700–800 m depth, a few even down to more than 1,500 m. Icefish have been shown to present organ-level adaptations on different levels to compensate for the ‘disadvantages’ of lacking respiratory pigments. These include a low metabolic rate, well perfused gills, increased blood volume, increased cardiac output, cutaneous uptake of oxygen, increased blood flow with low viscosity, enlarged capillaries, large heart, and increased skin vascularity. Biological features, such as reproduction and growth, are not unique and are comparable to other notothenioids living in the same environment. Icefish produce large yolky eggs which have a diameter of more than 4 mm in most species. Consequently, the number of eggs produced is comparatively small and exceeds 10,000–20,000 eggs in only a few cases. With the exception of species of the genus Champsocephalus which mature at an age of 3 to 4 years, icefish do not attain maturity before they are 5–8 years old. Spawning period of most icefish species is autumn–winter. The incubation period spans from 2 to 3 months in the north of the Southern Ocean to more than 6 months close to the continent. Growth in icefish to the extent it is known is fairly rapid. They grow 6–10 cm in length per annum before they reach spawning maturity. Icefish feed primarily on krill and fish. Some icefish species were abundant enough to be exploited by commercial fisheries, primarily in the 1970s and 1980s with Champsocephalus gunnari as the main target species. Most stocks of this species had been overexploited by the beginning of the 1990s, some had further declined due to natural causes. Other species taken as by-catch species in fisheries were Chaenocephalus aceratus, Pseudochaenichthys georgianus, and Chionodraco rastrospinosus. Chaenodraco wilsoni was the only species exploited on a commercial scale in the high-Antarctic. Part I was published in the preceding issue of Polar Biology. DOI 10.1007/s00300-005-0019-z.     

Antarctic icefishes (Channichthyidae): a unique family of fishes. A review, Part I

Icefish or white-blooded fish are a family of species, unique among vertebrates in that they possess no haemoglobin. With the exception of one species which occurs on the southern Patagonian shelf, icefish live only in the cold-stable and oxygen-rich environment of the Southern Ocean. It is still questionable how old icefish are in evolutionary terms: they may not be older than 6 Ma, i.e. they evolved well after the Southern Ocean started to cool down or they are 15–20 Ma old and started to evolve some time after the formation of the Antarctic Circumpolar Current. Individuals of most icefish species with the exception of species of the genus Champsocephalus have been found down to 700–800 m depth, a few even down to more than 1,500 m. Icefish have been shown to present organ-level adaptations on different levels to compensate for the ‘disadvantages’ of lacking respiratory pigments. These include a low metabolic rate, well perfused gills, increased blood volume, increased cardiac output, cutaneous uptake of oxygen, increased blood flow with low viscosity, enlarged capillaries, large heart, and increased skin vascularity. Biological features, such as reproduction and growth, are not unique and are comparable to other notothenioids living in the same environment. Icefish produce large yolky eggs which have a diameter of more than 4 mm in most species. Consequently, the number of eggs produced is comparatively small and exceeds 10,000–20,000 eggs in only a few cases. With the exception of species of the genus Champsocephalus which mature at an age of 3 to 4 years, icefish do not attain maturity before they are 5–8 years old. Spawning period of most icefish species is autumn-winter. The incubation period spans from 2 to 3 months in the north of the Southern Ocean to more than 6 months close to the continent. Growth in icefish to the extent it is known is fairly rapid. They grow 6–10 cm in length per annum before they reach spawning maturity. Icefish feed primarily on krill and fish. Some icefish species were abundant enough to be exploited by commercial fisheries, primarily in the 1970s and 1980s with Champsocephalus gunnari as the main target species. Most stocks of this species had been overexploited by the beginning of the 1990s, some had further declined due to natural causes. Other species taken as by-catch species in fisheries were Chaenocephalus aceratus, Pseudochaenichthys georgianus, and Chionodraco rastrospinosus. Chaenodraco wilsoni was the only species exploited on a commercial scale in the high-Antarctic. Part II will be published in the following issue. DOI 10.1007/s00300-005-0020-6.     

Systematics of Nymphaea subgenus Hydrocallis (Nymphaeaceae). I. Four new species from the Neotropics

Four night-blooming water-lilies ofNymphaea subgenusHydrocallis,N. conardii, N. lingulata, N. novo-granatensis, andN. prolifera, are described from the American tropics.     

Afrotropical Polypedilum subgenus Tripodura, with a review of the subgenus (Diptera: Chironomidae)

Vårdal, H., Bjørlo, A. & Sæther, O. A. (2002). Afrotropical Polypedilum subgenus Tripodura, with a review of the subgenus (Diptera: Chironomidae). —Zoologica Scripta, 31, 331–402. A subgeneric diagnosis for all stages of the subgenus Tripodura Townes, 1 945 of the genus Polypedilum Kieffer, 1 912 is given. Nine new Afrotropical species of Tripodura are described: P.(T.)chelum Vårdal sp. n., P.(T.)amplificatus Bjørlo sp. n., P.(T.)patulum Bjørlo sp. n., P.(T.)spinalveum Vårdal sp. n., P.(T.)ewei Bjørlo sp. n., P.(T.)ogoouense Bjørlo sp. n., P.(T.)akani Bjørlo sp. n., P.(T.)dagombae Bjørlo sp. n., and P.(T.)amputatum Bjørlo sp. n.; all as male imagines only. P.(T.)alboguttatum Kieffer, P.(T.)albosignatum Kieffer, P.(T.)tropicum Kieffer, P.(T.)pruina Freeman, P.(T.)quinqueguttatum Kieffer, P.(T.) aegyptium Kieffer, P.(T.) tridens Freeman, P.(T.)allansoni Freeman, P.(T.)longicrus Kieffer, P.(T.)annulatipes Kieffer and P.(T.)abyssiniae Kieffer are re‐described as male and female imagines, while P.(T.)majiis Lehmann, P.(T.)subovatum Freeman, P.(T.)griseoguttatum Kieffer, P.(T.)aferum Lehmann and P.(T.)kijabense Freeman are re‐described as male imagines only. Keys to the male and the known female imagines of the 30 Afrotropical species in the subgenus are presented. A phylogenetic analysis based on all available information on Tripodura from all over the world (135 species) is presented and discussed. The monophyly of the subgenus Tripodura is confirmed. The subgenus can be divided into 20 groups with the acifer group forming the sister group of two larger assemblages of groups in the order acifer (titicacae (ginzansecundum ((aferum (ewei (malickianum (floridense (halterale, pullum)))))) (subovatum (labeculosum ((parascalaenum (allansoni (apfelbecki (udominatum, parvum))))) ((((alboguttatum, aegyptium) quinqueguttatum) annulatipes)). Only in the titicacae, halterale, pullum and apfelbecki groups are the larvae of more than one species described, while one larva is known in each of the subovatum, parascalaenum, aegyptium and quinqueguttatum groups. Three or more pupae are known only from the halterale, pullum, apfelbecki and aegyptium groups. Thus, the tentative nature of the group divisions is obvious. Geographical co‐evolutionary analyses (Brooks parsimony analyses) of the subgenus as a whole and of the major groups are performed and the areas most likely to be part of the original areas estimated. Most probably, eastern South America and Africa were part of the ancestral area. There are multiple sister‐group relationships and generalized tracks between South and East Asia and Africa, between Africa and the Palaearctic region, between South and East Asia, between tropical Brazil and Africa, between East Asia and North America across a former Beringian land bridge, and between the Indo‐West Pacific region and New Zealand, but no evidence for transantarctic relationships.     

A new species of Brickellia,subgenus Phanerostylis (Asteraceae)

Brickellia nesomii, a new species from northeastern Mexico, is described. It belongs to the subgenus Phanerostylis, which Gray originally placed in Eupatorium; King and Robinson elevated the taxon to generic rank; it is herein kept at the subgeneric level but transferred to Brickellia. Reasons for this transfer are given. Barroetea glutinosa, positioned by King and Robinson in Phanerostylis, is excluded.     

Revision of the orchid bee subgenus Euglossella (Hymenoptera, Apidae), Part I, The decorata species group

Euglossella, one of the most distinctive subgenera of orchid bees of the genus Euglossa, is composed of two characteristic assemblages of species, one of them comprising bees bearing the strongly metallic integument trademark of the genus (viridis species group), and the other consisting of bees with a brown integument shaded with metallic iridescence (decorata species group). Here we provide the first of two parts of a revision of Euglossella, providing diagnostic definitions for the subgenus, the decorata species group, and all the species included therein. Six species are included in the decorata group, one new: Euglossa (Euglossella) aurantia, sp. n.; Euglossa (Euglossella) apiformis Schrottky, resurrected status; Euglossa (Euglossella) decorata Smith, revised status; Euglossa (Euglossella) singularis Mocsáry, revised status; Euglossa (Euglossella) cosmodora Hinojosa-Díaz and Engel; and Euglossa (Euglossella) perpulchra Moure and Schlindwein. Euglossa meliponoides Ducke and Euglossa urarina Hinojosa-Díaz and Engel are newly synonymized under Euglossa decorata, Euglossa decorata ruficauda Cockerell is synonymized under Euglossa singularis, and a neotype is designated for Euglossa apiformis.     

Occurrence of the subgenus Acanthosentis Verma & Datta, 1929 (Acanthocephala: Quadrigyridae) in Japan, with the description of Acanthogyrus (Acanthosentis) alternatspinus n. sp. and A. (A.) parareceptaclis n. sp. from Lake Biwa drainage fishes and a key to the species of the subgenus

All 44 described species of the subgenus Acanthosentis Varma & Datta, 1929 are recognised as valid. These include two new species, Acanthogyrus (Acanthosentis)alternatspinus n. sp. from Rhodeus ocellatus ocellatus (Kner) (Cyprinidae) and A. (A.) parareceptaclis n. sp. from Cobitis biwae Jordan & Snyder (Cobitidae) in the Lake Biwa drainage, Japan. These are the first representatives of the subgenus Acanthosentis recorded from Japan. Most other species are found in the Indian subcontinent, but a few have been reported from China, elsewhere in Asia, Africa, Europe and Central America. Only A. (A.) alternatspinus has the lateral proboscis hooks in the apical and middle circles markedly displaced posteriorly but of equal size to the other hooks in the same circles and multi-branched lemnisci. Acanthogyrus (A.) parareceptaclis uniquely possesses parareceptacle structures in both sexes as well as a pair of cone-shaped genital jackets flanking the vagina (vaginal sleeve). Two new names are provided: Acanthogyrus (Acanthosentis) adriaticus nom. nov. for A. (A.) lizae Orecchia, Paggi & Radujkovic, 1988 nec Wang, 1896, and A. (A.) cheni nom. nov. for A. (A.) coiliae (Yamaguti) sensu Chen et al. (1973). A review of the species composition of Acanthosentis is provided and a key to its species and zoogeographical notes are included.