Haruto Ishii

Distribution of salps near the South Shetland Islands during austral summer, 1990–1991 with special reference to krill distribution

Distribution and biomass of salps and Antarctic krill (Euphausia superba) were investigated near the South Shetland Islands during austral summer 1990–1991. Salp biomass ranged between 0 and 556 mgC·m−3 and was greatest at a station in the Bransfield Strait in late December 1990. Salp biomass was lower than that of E. superba. Two species of salps; Salpa thompsoni and Ihlea racovitzai were found, and the former was dominant numerically. Spatial distribution and generation composition of these two species was different. Spatial distributions of salps and E. superba did not overlap particularly so the January–February period. While E. superba was found mainly in the coastal area which showed high-chlorophyll a values, salps exhibited high biomass in the oceanic area with low chlorophyll a concentrations. Predation by salps on small krill and the competitive removal of food by them, are discussed as potential reasons for the relatively low abundance of E. superba at the stations where salps were present in great numbers.

In situ estimation of ephyrae liberated from polyps of Aurelia aurita using settling plates in Tokyo Bay, Japan

The continuous changes in the number of newly established polyps of Aurelia aurita (L.) on settling plates under natural conditions were observed from August 1998 to September 1999 in Tokyo Bay, Japan. A sharp decline in survivorship of newly settled polyps was observed within the first few days, however, survivorship of polyps settled in October increased by budding up to 399% after two months. The number of discs in each strobila varied from 1 to 6, however, most of the strobilae formed single discs. The percentage ratios of the total number of ephyrae to the initial number of polyps on settling plates were generally lower than 10%, but the highest ratio of 594.4% was estimated for the polyps settled in October. It is considered that most of the liberated ephyrae originate from the polyps settled in October in Tokyo Bay. This study suggests that the occurrence of ripe medusae with planula larvae throughout the year contributes to the success of settlement and growth of the polyp stage in Tokyo Bay.

In situ feeding rhythms of herbivorous copepods, and the effect of starvation

In situ diel variations in gut pigment contents of neritic (Acartia omorii andPseudocalanus minutus) and oceanic copepods (Calanus plumchrus andC. cristatus) were analyzed.A. omorii andP. minutus were sampled in Onagawa Bay on the east coast of Japan in May and August 1987, andC. plumchrus andC. cristatus were sampled in the Bering Sea in June 1986. Gut pigments were generally high at night, and bimodal feeding rhythms were observed in all species. The first peak of gut pigments occurred between sunset and midnight and was followed by a midnight decrease in gut pigment levels, resulting in eventual evacuation of the gut. The second peak was observed a few hours after sunrise. Incubation experiments indicated that ingestion rates of starved copepods were higher than those of acclimated copepods. This phenomenon was most notable at high food concentrations. Gut pigments of starved copepods rapidly increased after exposure to high concentrations of culturedThalassiosira decipiens. These findings suggest that in situ feeding behavior of herbivorous copepods includes periods of cessation or reduction in feeding during the night, and consequently, feeding activity is periodically enhanced with starvation. Starvation enhanced feeding behavior is most obvious in the large oceanic species,C. plumchrus andC. cristatus and is not distinct in small coastal species such asA. omorii.

Predation by the Phyllosoma Larva of Ibacus novemdentatus on Various Kinds of Venomous Jellyfish

The phyllosoma, a larva of spiny and slipper lobsters, has an exceptionally flat body and long appendages. It is known to associate with several species of cnidarian jellyfish, a behavior that is not rare in crustaceans. Indeed, phyllosomas clinging onto jellyfish have been observed both in the laboratory and in the natural environment. Wild phyllosomas have been found to contain jellyfish tissues in their hepatopancreas and feces, suggesting that the larvae utilize jellyfish as a food source; however, how they capture jellyfish and what species of jellyfish they prefer have rarely been investigated. The few previous studies conducted have suggested that phyllosomas have a high specificity for jellyfish (preying on only a few species); in contrast, the results of our study indicate that specificity is low. We show that phyllosomas prey on a variety of jellyfish species including deadly stinging types, on a variety of jellyfish developmental stages, and on various parts of the jellyfish body. When making contact with a jellyfish, phyllosomas first cling onto its exumbrella, feed on its tentacles or oral arms, and then consume the exumbrella. Phyllosomas may be capable of defending themselves against any types of nematocyst sting, and it is likely that they have evolved to utilize venomous jellyfish as a food in the open sea, where food may be scarce.

Metabolic rates and elemental composition of the Antarctic krill, Euphausia superba dana

Respiration rates of the Antarctic krill, Euphausia superba, have previously been measured by a number of scientists (e.g. Rakusa-Suszczewski and Opalinski 1978; Kils 1978/79; Ikeda and Hing Fay 1981; Ikeda and Mitchell 1982; Segawa et al. 1982; Hirche 1983; Ikeda 1984), but reports on their excretion rates (ammonia and phosphate) and elemental composition are not many (Ikeda and Mitchell 1982; Ikeda 1984). The present paper provides some additional informations on the metabolic rates and elemental composition (C, N, P) of the Antarctic krill. Experiments were carried out on board the TV Umitaka Maru during her 31st cruise (SIBEX) to the Antarctic Ocean in austral summer 1983/84. As described in our previous paper (Ishii et al. 1985), live krill (juveniles and adults) were collected whenever surface swarms were encountered (Table 1). The krill were transferred to a 500-1 plastic container and pre-incubated in ambient seawater and food on deck for at least 24 h under natural light and temperature conditions until the experiments commenced, in order to reduce variability of metabolic rates caused by the shock of collection. Particle concentrations of this pre-incubation seawater ranged be-

Distribution of biogenic silica and particulate organic matter in coastal and oceanic surface waters off the South Shetland Islands in summer

Biogenic silica (BSi), lithogenic silica (LSi), particiulate organic carbon (POC) and nitrogen (PON), and chlorophyll a (Chl a) concentration levels were measured in the surface waters (<100 m) off the northern coast of the South Shetland Islands in summer 1991. High concentration levels of BSi and LSi were recorded in the oceanic area and the coastal area, respectively. However, marked regional differences were not observed for POC, PON and Chl a concentrations. The mean BSi/POC atomic ratio (±SD) in the oceanic area (0.27±0.17) was 6 times that in the coastal area (0.045±0.020), except for the bloom situation (0.19±0.029). In contrast, the mean POC/PON atomic ratio was not significantly different in the coastal area (5.9±1.4) and the oceanic area (5.2±1.7). Nitzschia spp. were the dominant diatoms in the oceanic area but not in the coastal area. High BSi/POC ratios have been reported for blooms dominated by Nitzschia spp. even in the coastal regions of the Antarctic Ocean. The area difference in the BSi/POC ratios was probably related to the difference in species composition of phytoplankton and not to regional contrast. This species contributes significantly to high BSi/POC ratios in the Antarctic Ocean.