Environmental determinants of growth rates for larval Japanese anchovy Engraulis japonicus in different waters

Do disparate mechanisms determine growth rates of fish larvae in the different regions? The relationship between growth rates and environmental factors (sea temperature and food availability) was examined for larval Japanese anchovy Engraulis japonicus in geographically and environmentally different waters, through sagittal otolith microstructure analysis. Recent 3‐day mean growth rates directly before capture were positively related with sea‐surface temperature (SST) but not with food availability (plankton density) for the larvae in the Kuroshio Extension and Kuroshio–Oyashio transition regions of the western North Pacific. On the contrary, variations in recent growth rates were attributed to food availability (plankton density) as well as SST for the larvae in the East China Sea. In the shirasu fishing ground in Sagami Bay, larval growth rates were variable under the influences of both SST and food availability (feeding incidence). On the surface, the growth–environment relationships seemed to differ among regions. However, a definite general pattern of the dome‐shaped relationship between recent growth rates and SST was observed when all the regions were combined. Growth rates were similar even among clearly different regions if at the same SST. Overall, growth rates roughly increased with SST until they reached the maximum at SST of 21–22°C (i.e. optimal growth temperature), and declined when SST went over 21–22°C. On the contrary, no clear relationship was observed between growth rate and plankton density or between SST and plankton density. Therefore, the apparent among‐region differences would be firstly caused by the differences in regional SST range. The systematic mechanism of growth determination for widespread pelagic fish species larvae would be run by primarily sea temperature and secondarily food availability, at the species level.     

Patchiness structure and mortality of Pacific saury Cololabis saira larvae in the northwestern Pacific

Patchiness structure and mortality rates of Pacific saury Cololabis saira larvae were estimated in the frontal area of the Kuroshio Extension in spring 2000 and 2001. Drogued GPS buoys, which were used as Lagrangian reference points, were deployed to mark dense patches of saury larvae and a series of samplings was conducted using a neuston net around the buoys during the night over a period of several days. A total of 225 tows were conducted and 11 690 specimens were sampled during four buoy tracking. Despite the occurrence of water diffusion, patchiness density, distance between adjacent patches and patch size estimated by geostatistical analysis did not drastically change during the buoy tracking and these parameters were robust for the difference of variogram models and the threshold larval density defining patchiness. Such a stability of the patchiness allowed the estimation of larval mortality from the decrease of larval density for different size classes with respect to individual growth based on the samples taken repeatedly during the buoy tracking. Although low or negative values were obtained for the larvae right after hatching, probably due to continuous hatching, the estimates of mortality then increased and became stable in the range of 23–37% day⁻¹ with a small standard deviation until their knob length reached to 36 mm. In situ information on the patchiness structure and larval mortality provides crucial parameters for simulating the recruitment process of small pelagic fishes in high-resolution hydrodynamic models.     

Observations on the effect of salinity and photon fluence rate on the induction of sporulation and rhizoid formation in the green alga Enteromorpha prolifera (Müller) J. Agardh (Chlorophyta, Ulvales)

ABSTRACT: Although most members of the genus Enteromorpha are important edible green algae, some species are also potentially economically valuable crops. Samples of E. prolifera were obtained from the Yoshino River estuary, Tokushima, Japan and cultured in laboratory conditions at 10°C, a salinity of 20 psu, under white light with 12 h light : 12 h dark cycle and at a photon fluence rate (PFR) of 40 μmol/m² per s for 30 days. In the present study, the effect of salinity and PFR on the induction of reproductive cells and rhizoid formation were investigated. Synchronous formation of swarmers by thalli was induced in excised disks of 1.2 mm diameter after 2–5 days incubation. The optimum salinity for maturation of reproductive cells was between 5.0 and 52.0 psu, and between 13.2 and 45.3 psu for swarmer release, although the lower limit for swarmer release was 5.0 psu. Maturation of reproductive cells and swarmer release required a PFR higher than 16 μmol/m² per s. The minimum PFR for swarmer release was 8 μmol/m² per s. Many rhizoids were formed between 1.6 and 52.0 psu and photon fluence rates between 8 and 320 μmol/m² per s. Rhizoids were formed in a polarized manner.     

A modeling approach to evaluate growth and movement for recruitment success of Japanese sardine (Sardinops melanostictus) in the western Pacific

A two‐dimensional individual‐based fish movement model coupled with fish bioenergetics was developed to simulate the observed migration and growth of Japanese sardine (Sardinops melanostictus) in the western North Pacific. In the model, derived from the observed ocean–environmental data as the driving force, fish movement was adapted as a kinesis behavior. The model successfully simulated the observed transport patterns during the egg and larval stages and the northward migrations during the juvenile stage in 2005, 2006 and 2007. The model results showed that both temperature during the larval stage in the Kuroshio Extension and the prey availability during the early juvenile stage in the Kuroshio–Oyashio transitional area are important factors for growth of Japanese sardine. In autumn, the observed juvenile sardine were mainly distributed in the subarctic water region off the Kuril Islands, which is an area (158–165°E, 43–47°N) with a high chlorophyll‐a (Chl‐a) concentration. The model reproduced the fish distribution, which has a high density in this region. The high Chl‐a concentration area in autumn may contribute to increasing the survival rate of Japanese sardine by cascading up the food chain, from the high primary production, and is an important habitat for recruitment success of Japanese sardine.     

Diel vertical migration of myctophid fishes (Family Myctophidae) in the transitional waters of the western North Pacific

The diel vertical migration patterns of adult myctophid fishes were determined in the transitional waters of the western North Pacific off Japan, using day–night sampling from 20 to 700 m depths with a commercial otter trawl in the summer of 1995. A total of 12 species belonging to 9 genera were collected. Four patterns were recognized in the diel vertical migration of 11 of the 12 species. (1) Migrants showing clear day–night habitat separation with peak abundance above 200 m at night: Symbolophorus californiensis, Tarletonbeania taylori, Notoscopelus japonicus, Diaphus theta, Ceratoscopelus warmingi, and Diaphus gigas. (2) Semi-migrants, in which part of the population often remains in the daytime habitat at night. The distribution depths of migratory and nonmigratory individuals do not overlap: Stenobrachius leucopsarus . (3) Passive-migrants, in which there is no separation of day–night habitats, but the upper limit of daytime distribution depth shifts to a shallower layer at night, probably as the fish follow migratory prey: Lampanyctus jordani . (4) Nonmigrants: Stenobrachius nannochir, Lampanyctus regalis (> 140 mm SL), and Protomyctophum thompsoni . The day–night habitat temperature ranges are also given for the 11 species. No remarkable east–west differences were seen in the vertical migration patterns compared with previous knowledge of eight of these species in the eastern Pacific. The diel migration patterns are newly described for three other species endemic to the western Pacific. The standing stock of myctophids in the study area was conservatively estimated at 18.5 ± 4.7 g m⁻² (avg. ± SD).