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The spawning grounds of the chub mackerel (Scomber japonicus) and spotted mackerel (Scomber australasicus) in the East China Sea were estimated based on catch statistics of the Japanese large- and medium-type purse seine fishery from 1992 to 2006. Biometric data were obtained from specimens caught by purse seiners in the East China Sea from 1998 to 2006. Gonadosomatic index (GSI) at 50% sexual maturity of chub mackerel and spotted mackerel females was 2.5 and 2.6, respectively. Using this criterion for GSI, chub mackerel larger than 275 mm and spotted mackerel larger than 310 mm in fork length were considered to be mature. Mature chub mackerel was observed in the area of 15-22degC sea surface temperature (SST), and mature spotted mackerel was observed in the area of 17-25degC SST. The spawning period of chub mackerel ranged from February to June, and that of spotted mackerel ranged from February to May in the East China Sea. The spawning grounds were estimated from the distributions of catch per unit effort (CPUE) of spawners and SST. As a result, the spawning ground of chub mackerel was estimated to be in the central and southern part of the East China Sea and the area west of Kyushu in February, March, and April, and in the central part of the East China Sea, the area west of Kyushu and Tsushima Straight in May, and in Tsushima Straight and western part of the Sea of Japan in June. The spawning ground of spotted mackerel was estimated to be in the central and southern part of the East China Sea and southern coastal area of Kyushu in February, March, and April, and the central and southern part of the East China Sea and the area west of Kyushu in May.

:  Anadromous Coilia ectenes was sampled from the Yangtze estuary at Chongming and two of the primary upstream spawning grounds at Jingjiang and Anqing in April, May, June and August 2006. Gonad development was analyzed for females. In April, fish were collected in the estuary and at Jingjiang, but not at Anqing. No female was mature (gonad at stages IV or V) at either location. In May, 45% of the females were mature in the estuary, 9% at Jingjiang and 5% at Anqing. In June, 86% were mature in the estuary, 83% at Jingjiang and 7% at Anqing. In August, C. ectenes was absent at Jingjiang. No female was mature in the estuary, and all females were mature at Anqing. Absolute fecundity (AF) increased significantly with standard length (SL) by a power function AF = 2.27 × 10−6 × SL2.67 (r2 = 0.57, n = 48, P < 0.05). Mature females in the estuary were smaller than those at Jingjiang and Anqing. Conservation of spawners in the upstream spawning grounds is important because they have a size‐related fecundity advantage over the smaller spawners in the estuary.

A ceramic coral settlement device (CSD) was developed to raise juvenile corals in situ in preparation for transplantation. The CSD is designed to be deployed in the water before mass spawning of corals, allowing larvae to settle and grow on the CSD before it is fixed to the reef structure. CSDs were aggregated and fixed on 0.2-m 2 frames (either 648 or 720 CSDs per frame) and deployed in the Sekisei Lagoon around the full moons of April and May in 2002. Seven frames were collected in August 2002 and settled corals were counted in the laboratory. The maximum number of coral colonies settled on CSDs in one frame was 617, with 94% belonging to the genus Acropora . The aggregated CSDs successfully functioned as a coral settlement substratum, with more appropriate arrangement of CSDs on the frame, enabling greater exposure to sunlight and currents, which is expected to increase the amount of settlement.

To determine the reproductive season of the giant jellyfish Nemopilema nomurai, we investigated gonadal maturity in specimens collected from the East China Sea, Korea Strait, Wakasa Bay, and the Shonai Coast of Yamagata Prefecture. After the sex of the samples was determined, the long axis of at least 256 oocytes from each female was measured. In specimens collected from the coast of Japan in 2005 and in 2006, all gonads were sufficiently developed to determine sex. However, 18 of the 20 specimens from the East China Sea collected in July 2005 were immature, and sex could not be determined. The maximum and third quartile of oocyte length had a significant correlation with days elapsed from 30 June, but they were not related to bell diameter. Observations of gonad tissue sections of specimens collected in Wakasa Bay in 2006 confirmed that oocyte length was a good proxy for female maturity. Male maturity could also be determined. In conclusion, the sex of all of the small-sized medusae collected along the coast of Japan was determinable, and their gonads were at various stages of development up to fully mature. Therefore, the occurrence of small-sized jellyfish during the autumn in Wakasa Bay is not caused by recruitment of young population from the nearby coast.

We examined the spawning sites of several gobiid fishes in the subtidal zone of a small temperate estuary and determined the relationship of the nest abundance of each species with several environmental conditions, including water temperature, salinity, median particle size, proportion of silt and clay, current width, maximum water depth, distance from each site to the river mouth, and density of objects (boulders, cobbles, empty oyster shells, and empty clam shells) in the water. During this study, we found 115 nests belonging to the following six species: Favonigobius gymnauchen, Tridentiger obscurus, Leucopsarion petersii, Acanthogobius lactipes, Rhinogobius giurinus, and Tridentiger trigonocephalus. Stepwise multiple regression analysis, which was used to determine the best model for the nest abundance of all species, revealed that the nest abundance of each species clearly increased with an increase in the density of spawning substrates, such as cobbles and bivalve shells. These results show that the density of spawning substrates is a crucial factor affecting the selection of spawning habitats by each species.

The presence of mudskipper eggs in an air-filled chamber was confirmed by direct endoscopic observation of intact burrows of Periophthalmodon schlosseri in a mudflat in Penang, Malaysia. For all five burrows from which video images of egg chambers were successfully obtained, the presence of air was unequivocally demonstrated by the existence of an air-water interface inside the chambers. Of these burrows, eggs were found in two, but not in the others. Eggs were laid uniformly in a monolayer on the inner top surface of the chamber. The much brighter color of the surface mud of the egg chambers than the surrounding mud, irrespective of the presence or absence of the eggs, suggested that the surface mud had been oxidized by deposited air.

The spawning season and grounds of red sea bream in Hiuchi-nada, the central part of the Seto Inland Sea, were described using a new method based on monoclonal antibodies for identifying Pagrus major eggs, and the daily egg production (standardized by the incubation time and survival rate) was estimated. At the peak of spawning (May), the ranges of sea temperature, salinity, and chlorophyll a where red sea bream eggs occurred were 14.8-17.4degC, 32.0-33.0, 0.5-4.4 microg/L, respectively. The main spawning grounds of the red sea bream were confirmed as being the areas near the Geiyo Islands, Misaki Peninsula, Saijyo, Niihama. The spatial spread of red sea bream eggs increased with the egg developmental stage. The ranges of daily egg production in 2005 and 2006 were 0.3-19.3 and 0.2-6.7 x 10E9 eggs/day, respectively. In Hiuchi-nada, aquaculture farms are located close to the spawning grounds, and the potential spawning population from the aquaculture farms equaled or exceeded that of the estimated spawning population obtained by the egg production method. Red sea bream eggs in Hiuchi-nada might be produced by both wild and aquaculture-based spawning populations.

Spawning migration patterns were compared between sympatric populations of the anadromous Japan Sea (JS) form and Pacific Ocean (PO) form of the threespine stickleback Gasterosteus aculeatus in the Lake Akkeshi-Bekanbeushi River system, eastern Hokkaido, Japan. In Akkeshi Bay and Lake Akkeshi, the JS form had longer collecting peak periods and more collection peaks than the PO form. Furthermore, although the PO form migrated upstream in freshwater habitats, the greater part of the JS form stayed in brackish waters before breeding. These findings suggest that the 2 forms have distinctly different spawning migration patterns and breeding grounds.

Fresh eggs of European perch, Perca fluviatilis L., were collected, in the form of egg ribbons, from females caught at the spawning grounds on the Odra River side canal Dziewoklicz, within the city limits of Szczecin, Poland. After fertilization eggs were fixed in formaldehyde. In the laboratory, the commonly accepted techniques were used to prepare samples for examination with a scanning electron microscope (SEM). The observations were photographically documented. A network of microtubules was observed closely below the surface of the gelatinous egg ribbon. These microtubules opened at the egg ribbon surface in the form of ring-like or nozzle-like pores. The gelatinous egg envelope of perch is a complex microtubular network that likely performs a skeletal role for the egg ribbon