New records of philometrids (Nematoda: Philometridae) from marine fishes off Japan, including description of Philometra kidakoi sp. n. and Congerinema japonicum gen. et sp. n.

Occasional examinations of some marine fishes in Japan revealed, in addition to other parasites, the following eight species of philometrid nematodes (Philometridae) (all females only): Philometra kidakoi sp. n. from the ovary of Gymnothorax kidako (Temminck et Schlegel) (Muraenidae); Philometra pinnicola (Yamaguti, 1935) from the operculum of Epinephelus akaara (Temminck et Schlegel) (Serranidae); Philometra sebastisci Yamaguti, 1941 from the ovary of Sebastes cheni Barsukov (Scorpaenidae) (new host); Philometra madai Quiazon, Yoshinaga et Ogawa, 2008 from the ovary of Acanthopagrus schlegelii (Bleeker) (Sparidae) (new host); Philometra isaki Quiazon, Yoshinaga et Ogawa, 2008 from the ovary of Parapristipoma trilineatum (Thunberg) (Haemulidae); Philometra sp. from the ovary of Synanceia verrucosa Bloch et Schneider (Synanceiidae); Congerinema japonicum gen. et sp. n. from the subcutaneous tissue of Conger myriaster (Brevoort) (Congridae); and Clavinema mariae (Layman, 1930) from the operculum of Acentrogobius pflaumii (Bleeker) (Gobiidae). Specimens of all species are described based on light and scanning electron microscopical examinations. Philometra kidakoi sp. n. is the first gonad-infecting philometrid from the Muraenidae. The new monotypic genus Congerinema gen. n. is characterised by the unique net-like cuticular ornamentation on the female body. Clavinema mariae is considered to be a complex of several cryptic species and a need of the discovery of conspecific males is stressed (this also concerns other philometrid species with unknown males). At present, the fauna of philometrid nematodes parasitising marine fishes in Japanese waters is represented by 22 nominal species belonging to four genera.

A Simplified Gas Chromatographic Fatty-Acid Analysis by the Direct Saponification/Methylation Procedure and Its Application on Wild Tuna Larvae.

A method for the direct preparation of fatty-acid methyl esters (FAME) was simplified for fatty-acid analysis of a single fish larva using gas chromatography (GC). The method included the isolation of a larval trunk and drying in a glass vial, followed by saponification of all the contents without prior lipid extraction. Thereafter, the fatty acids released were methylated by trimethylsilyldiazomethane. This method has advantages over another method, direct acid-catalyzed transesterification, because both the saponification and methylation at room temperature can reduce loss of unsaturated fatty acids and formation of artifacts unavoidable in acidic reaction at high temperature. GC of the products showed that the simplified method can yield methyl esters without artifacts interfering analysis. More than 50 fatty acids were determined, which are twice as many as those previously analyzed using high-performance liquid chromatography. Observation of consistent small impurities in GC of blank tests allowed the accurate determination of fatty acids by correcting the peak areas. Dry matter weights (<3 mg) and the total fatty-acid contents displayed a linear relationship. Fatty-acid analysis of wild larvae of bluefin tuna, yellowfin tuna, and skipjack tuna collected from the waters around Japan (n = 100) revealed that the eicosapentaenoic acid (EPA) level in bluefin tuna collected from the Japan Sea was significantly higher than that in the three species collected from Nansei Islands. The simplified direct saponification/methylation method will be a powerful tool for investigating growth and survival of individual larval tuna and other fish species.

Pelagic larval duration, growth rate, and population genetic structure of the tidepool snake moray Uropterygius micropterus around the southern Ryukyu Islands, Taiwan, and the central Philippines.

The relationships between pelagic larval duration (PLD) and geographic distribution patterns or population genetic structures of fishes remain obscure and highly variable among species. To further understand the early life history of the tidepool snake moray Uropterygius micropterus and the potential relationship between PLD and population genetic structure of this species, otolith microstructure and population genetics based on concatenated mtDNA sequence (cytochrome b and cytochrome oxidase subunit I, 1,336 bp) were analyzed for 195 specimens collected from eight locations around the southern Ryukyu Islands, Taiwan, and the central Philippines. Eels with longer PLD and lower otolith growth rates were observed at relatively higher latitudes with lower water temperatures (54.6 ± 7.7 days and 1.28 ± 0.16 µm day-1 on Ishigaki Island, Japan, vs. 43.9 ± 4.9 days and 1.60 ± 0.19 µm day-1 on Badian, the Philippines), suggesting that leptocephali grew faster and had shortened pelagic periods in warmer waters. Meanwhile, the eels along the southwest coast of Taiwan had relatively longer PLD (57.9 ± 10.5 days), which might be associated with the more complex ocean current systems compared to their counterparts collected along the east coast of Taiwan (52.6 ± 8.0 days). However, the southwestern and eastern Taiwan groups had similar otolith growth rates (1.33 ± 0.19 µm day-1 vs. 1.36 ± 0.16 µm day-1). Despite the intergroup variation in PLD, genetic analysis revealed fluent gene flow among the tidepool snake morays in the study regions, implying that intraspecies PLD variation had a weak effect on genetic structure. The leptocephalus stage might have ensured the widespread gene flow among the study areas and leptocephalus growth was likely influenced by regional water temperature.