Vertical distribution, life cycle, and developmental characteristics of the mesopelagic calanoid copepod Gaidius variabilis (Aetideidae) in the Oyashio region, western North Pacific Ocean

Vertical distribution, life cycle, and developmental characteristics of the mesopelagic copepod Gaidius variabilis Brodsky in the Oyashio region were investigated by combining analyses of field copepodite populations with laboratory-rearing data of egg hatching and naupliar development. Field samplings from five discrete depths between the surface and ≤2000 m were made approximately every month for 1 year. Most populations of G. variabilis occurred between 600 and 1000 m depth. A modest degree of reversed diel vertical migration behavior and some stage-specific depth-distribution patterns were noted. All copepodite stages were observed throughout the year, suggesting a year-round spawning of G. variabilis. From a prominent abundance peak of Copepodite Stage 1 (C1) seen in June to August, together with development times of eggs and nauplii obtained in laboratory-rearing experiments, the major spawning season was extrapolated to be April to June, the phytoplankton bloom season. Tracing the peak abundance of each copepodite stage (distinguishing males and females for C4 to C6), the generation times of males and females were deduced as 2 and 1 year, respectively. All between-stage increments in terms of wet-, dry-, and ash-free dry weights were greatest in C3/C4, and least in C5/C6 for both males and females. The increments in C3/C4 and C4/C5 were greater for males than for females, reflecting a longer stage duration of the males. These weights did not increase in C5/C6 males, possibly because feeding ceased in C6 males. These results for G. variabilis are compared with those for some mesopelagic copepods previously reported from other regions. Received: 25 October 1999 / Accepted: 20 March 2000     

Population dynamics and production of the planktonic copepods in a eutrophic inlet of the Inland Sea of Japan. II. Acartia omorii

Population dynamics and production of the calanoid copepod Acartia omorii Bradford were studied from November 1986 to November 1987 in Fukuyama Harbor, a eutrophic inlet of the Inland Sea of Japan. This species was present in the plankton from October to July (temperature range: 8.9 to 24.3°C), with peaks in February-March and June. During this period, nine generations could be detected, for which the mean population egg production rate and midstage abundance of each life stage older than naupliar Stage (N) II were determined to trace survival. The population suffered extremely high mortality during the early life stages: on average only 2.5% of the eggs produced recruited into NII. This large loss is probably concentrated within the egg stage, due to predation, including cannibalism, by omnivorous copepods, in addition to sinking loss of eggs in the water column. However, the mortality from NII to copepodite Stage (C) V was negligible, indicating low predation pressure by large carnivores. The biomass of A. omorii showed marked seasonal variations in parallel with numerical abundance. The instantaneous growth rate of each stage increased exponentially with increasing temperature. The integrated production rate of A. omorii from 7 November 1986 to 21 July 1987 was 749 mg Cm^-3 or 5.62 g Cm^-2     

Abundances,growth rates,and production of tropical neritic copepods off Kingston,Jamaica

Weekly samples were collected near Kingston, Jamaica in 27 m vertical hauls, using 200 and 64µm mesh plankton nets, from July 1985 to January 1987. Thirtytwo copepod species were identified; nauplii and all copepodite stages were enumerated. Total copepod abundance ranged from 2.56 to 87.3 × 10⁴ m^–2. The annual abundance cycle was bimodal with peaks in October–November and May–June corresponding to the rainy seasons. Mean annual copepodite biomass was 0.15 g AFDW m^–2 ranging from 0.03 to 0.41 g AFDW m^–2. Mean generation time (from egg to adult) at 28°C was 19.5 d for the common speciesCentropages velificatus, Paracalanus aculeatus, andTemora turbinata. Isochronal development was demonstrated for copepodites ofP. aculeatus andT. turbinata, but not forC. velificatus. Mean daily specific growth rates (G) were 0.63, 0.63, and 0.48 d^–1 forC. velificatus, P. aculeatus, andT. turbinata, respectively. In general, daily specific growth rates decreased in the later copepodite stages. Thus, it is postulated that growth of later stages and egg production may be food limited. Annual copepodite production was estimated as 419 kJ m^–2 yr^–1, while annual exuvial production and naupliar production were 35 and 50 kJ m^–2 yr^–1, respectively. Egg production was estimated as 44% (184 kJ m^–2 yr^–1) of the total copepodite production. Thus, mean total annual copepod production was 688 kJ m^–2 yr^–1. This estimate is within the range of copepod production estimates in coastal temperate regions.     

Annual biomass and production of the oceanic copepod community off Discovery Bay,Jamaica

Monthly samples were collected in oceanic waters off Discovery Bay, Jamaica, in 60- and 200-m vertical hauls, using 200- and 64-m mesh plankton nets, from June 1989 to July 1991. Length-weight regressions were derived for twelve genera of copepods (R²=0.79 to 0.97). For eight occasions spanning the study period, biomass estimates generated from these length-weight regressions differed by only 3% from direct weight determinations. The mean ash content of copepods was 7.1%, and the energy density was 20.8 kJ g^-1 ash-free dry weight (AFDW). Mean annual biomass of the total copepod community in the upper 60 m was 1.83 mg AFDW m^-3 (range 1.14 to 2.89 mg AFDW m^-3), and for the 200-m water column was 0.96 mg AFDW m^-3 (range 0.12 to 1.99 mg AFDW m^-3). Estimates of generation times for five common taxa ranged from 16.1 to 33.4 d. None of the taxa investigated displayed isochronal development; in general, stage duration increased in later copepodite stages. Weight increments showed a significant decrease in later copepodite stages, but with strong reversal of the trend from stage 5 to adult female in most species. Daily specific growth rates also declined in later copepodite stages, and ranged from 1.49 d^-1 in stage 1–2 Paracalanus/Clausocalanus spp. to 0.04 in stage 5-female of Oithona plumifera. Progressive food limitation of somatic copepodite growth and egg production is postulated. Naupliar production was 50.4 to 59.5% of copepodite production, and egg production was 35.1 to 27.7% of copepodite production in the 60-and 200-m water columns, respectively. Total annual copepod production, including copepodites, nauplii, eggs and exuviae, was 160 kJ m^-2 yr^-1 for the upper 60 m and 304 kJ m^-2 yr^-1 for the upper 200 m. Secondary production of the copepod community in oceanic waters off Discovery Bay approaches 50% of the corresponding value in tropical neritic waters.     

Seasonal variations in distribution and population structure of Microcalanus pygmaeus and Ctenocalanus citer (Copepoda: Calanoida) in the eastern Weddell Sea,Antarctica

The abundance, vertical distribution and population structure of two important small calanoid copepod species, Microcalanus pygmaeus (G. O. Sars) and Ctenocalanus citer Heron and Bowman, were studied in the eastern Weddell Sea in summer (January/February 1985), in late winter/early spring (October/November 1986) and in autumn (April/May 1992). The population of Microcalanus pygmaeus consisted mainly of copepodite stages CII and CIII in late winter/early spring and were concentrated between 500 and 200 m depth. In summer, stage CIV was the modal stage and the bulk of the population had ascended above 300 m. In autumn the population structure was bimodal with CI and CV dominating. Most of the population was concentrated between 300 and 200 m. In all investigation periods M. pygmaeus had their maximal concentrations in the thermo-pycnocline. The developmental stages CIII to CV of Ctenocalanus citer formed the bulk of the population in late winter/early spring. In October all developmental stages had their main distribution between 500 and 200 m, except females, which were concentrated in the upper 50 m. In November most of the population occurred between 200 and 50 m. The summer population was concentrated in the upper 50 m, and numbers increased dramatically as the new cohort hatched. Copepodite stages CII and CIII dominated the population at the end of January, while CIV dominated 2 wk later. In autumn, CV was the modal stage. The majority of the population was concentrated in the upper 100 m, but there was an increase in abundance below 300 m compared to summer. Age structure changed with depth with a younger surface population and an older one in deeper water layers. The seasonal change in number of M. pygmaeus is much smaller than that of C. citer; the summer:winter:autumn ratio of the former being about one, whereas the winter:summer/autumn of the latter was about nine. Early copepodite stages and adults of M. pygmaeus occurred throughout all investigation periods. The large proportion of early copepodite stages in April and in mid-October suggests autumn and early to midwinter breeding. Apparently, M. pygmaeus may reproduce and grow year-round or perhaps has a 2-yr life-cycle. In contrast, the dramatic increase in abundance of early copepodite stages of C. citer in summer suggests springtime reproduction.     

Some aspects of the life history of the subarctic copepodNeocalanus cristatus (Calanoida) in Sagami Bay,central Japan

A typical subarctic copepod,Neocalanus cristatus, occurred in the mesopelagic layer (500 to 1000 m) in Sagami Bay, central Japan, throughout the year. Specimens were collected from 1982 to 1986. A small number of adult females were distributed from 800 to 900 m only, but no adult males were collected. This species appeared to be abundant in April and August, when intermediate Oyashio water flowed strongly into Sagami Bay. Mean prosome lengths of copepodite stages IV and V and adults were 4.33, 6.87 and 6.87 mm, respectively. The condition factor [wet wt/(prosome length)³ × 100] of copepodite stage V did not vary remarkably, and mean values ranged from 4.7 to 5.0. Prosome length, body weight and condition factor ofN. cristatus collected from Sagami Bay were smaller than those of copepods in the northern North Pacific.N. cristatus transported from the north cannot molt to adult stages (except for those originating in mesopelagic waters) due to the adverse environmental conditions in Sagami Bay; instead, they die in the mesopelagic layer and sink to the bathypelagic layer (1 000 to 1 400 m), close to the bottom. Since nauplii and early copepodite stages did not occur in any season,N. cristatus probably do not reproduce in Sagami Bay.     

Growth and production of the inshore marine copepod Pseudodiaptomus marinus in the central part of the Inland Sea of Japan

The growth and production of the inshore marine copepod Pseudodiaptomus marinus was studied in the central part of the Inland Sea of Japan. The stage-specific growth rate was determined under controlled laboratory conditions by examining the length-weight relationship and development rates at various temperatures. The stage duration was short and constant from NII to CII, beyond which development was retarded. Males developed faster than females in CIV and CV. The specific growth rate was highest in copepodite stages followed by the nauplii and adult females (=egg production rate). The daily production of P. marinus was estimated from the stage-specific growth rate and stage-specific abundance in nature as the sum of the individual stages. The production changed seasonally with water temperature and population biomass. Daily production and biomass (P/B) ratios increased linearly with temperature. Total annual production was 20.7 mg C m^-3 yr^-1.     

Overwintering strategies of dominant calanoid copepods in the German Bight, southern North Sea

Abundance, stage composition and reproductive parameters (egg production, egg viability, proportion of spawning females) of the four copepod species Acartia clausi, Centropages hamatus, C. typicus and Temora longicornis were measured at the long term sampling station Helgoland Roads (German Bight, southern North Sea) from September 2003 to May 2004 to study their overwintering strategies. A. clausi was overwintering as females with arrested reproduction from November to January. T. longicornis, which is known to produce resting eggs in the North Sea, had a pelagic population with all developmental stages present during winter and reproductive rates closely related to food concentrations. Although their females produced eggs in response to ambient food conditions, both C. hamatus and C. typicus were rare in the pelagic. The C. hamatus population returned in May, probably from resting eggs, whereas C. typicus depended on advection. The Centropages species seemed to be less adapted to pelagic life in winter than A. clausi and T. longicornis. Sporadic occurrence of large numbers of nauplii and young copepodids of A. clausi and Centropages spp. pointed to different overwintering strategies or more successful survival in adjacent regions and advection of them into the waters around Helgoland island. While A. clausi was decoupled from environmental conditions in late autumn and winter, the other species were able to respond to variations in the food environment. Thus, egg production of T. longicornis increased during an unusual autumn diatom bloom.     

Population dynamics of Euterpina acutifrons (Copepoda: Harpacticoida) from North Inlet,South Carolina,with reference to Dimorphic Males

The population dynamics of Euterpina acutifrons (Dana), a pelagic, harpacticoid copepod, are summarized in a life table based on field data. Highest mortality occurred in the last naupliar stage (NVI) and the first copepodite stage (CI). Overall survival in the field was 0.06% from the first naupliar stage (NI) to adult (CVI). The net reproductive rate (R _o=55.590) and intrinsic rate of increase (I _m=0.28) were sufficiently high to maintain a population with such a low survival rate in nature. E. acutifrons was present and breeding in the field from April through December. Low temperatures limited breeding, which began when the temperature reached 16.5°C and ceased when it fell to 11°C. Optimum temperature for North Inlet E. acutifrons was 25°C, with a maximum laboratory survival of 15.3% and a generation time of 10.3 days. Generation time in the field (20°C) was 14 days. Temperature also affected the abundance of dimorphic males. Small males were always most abundant, but peaked during the coldest month; large males became equal in abundance only during the varmest months.Contribution No. 298 from the Belle W. Baruch Institute for Marine Biology and Coastal Research.     

Physioecology of zooplankton. II. Effects of phytoplankton concentration,temperature, and body size on the development and molting rates of Calanus pacificus and Pseudocalanus sp.

Developmental time and stage duration for Calanus pacificus Brodsky and Pseudocalanus sp. and the rate of loss of body carbon by molting for C. pacificus were estimated for copepodite stages cultured under various combinations of phytoplankton concentration and temperature. Mean development time and stage duration for C. pacificus decreased hyperbolically with increasing food concentration, and the minimum time required for reaching a given stage decreased logarithmically with a logarithmic increase in temperature. Low temperature retarded the development of early stages proportionally more than that of late stages, and stage duration increased logarithmically with increasing body weight. Therefore, copepodite development was not isochronal. The rate of loss of body carbon by molting was small, ranging from 0.2 to 2% day^-1. This rate increased hyperbolically with food concentration and was linearly related to the growth rate. The critical food concentration for the rates of development and molting increased with temperature and stage of development, but these rates were less dependent on food concentration than the growth rate. The development rate of Pseudocalanus sp. was higher than that of C. pacificus, and was less influenced by changes in food concentration and temperature. It is postulated that the inverse relationship between temperature and body size results from a differential effect of temperature and body size on the rates of growth and development. That is, with increasing body size the growth rate tends to become temperature-independent, but the development rate remains proportional to temperature. Thus, copepodites growing at low temperature can experience a greater weight increment between molting periods than individuals growing at high temperature, because the growth rate is similar at all temperatures but stage duration is longer at low temperature.Contribution No. 1128 from the Department of Oceanography, University of Washington, Seattle, Washington 98195, USA     

Growth and development of Calanus spp. (Copepoda) during spring phytoplankton succession in the North Sea

Experiments were carried out to determine growth and development rates of the herbivorous copepod Calanus finmarchicus (Gunnerus) under natural conditions during the phytoplankton spring bloom in the northern North Sea. From 28 April to 25 May 1983 copepodite stages I, IV and V were incubated for a 3-d period on board a ship in vessels with naturally occurring phytoplankton or cultured algae as food. Highest rates of growth and development were achieved while the diatom Chaetoceros sp. was the dominant phytoplankton organism. These rates decreased considerably when this chain-forming diatom was succeeded after one week by the small-celled diatom Thalassiosira conferta. Again one week later, during the bloom of the succeeding colonial microflagellate Corymbellus aureus, copepodite stage IV still managed to maintain moderate rates of growth and development, but these rates dropped to almost zero in CV, suggesting the start of a resting stage. Nevertheless, brood collected from this generation and from Calanus helgolandicus (Claus) was raised in the laboratory to the adult stage at high speed. Since temperature and the total phytoplankton concentration in the sea remained almost constant it seems that the retardation and arrestment of growth and development were an immediate response to a qualitative change of the food composition related to the successive blooms of different algal species.     

Molting rates and cohort development of Calanus finmarchicus and C. glacialis in the sea off southwest Nova Scotia

Species of Calanus were sampled at stations off southwest Nova Scotia during an 8-d cruise in June, 1982. A simple model using shipboard measurement of molting rates of predominant copepodite stages accurately predicted the changes in cohort structure that occurred at stations along a transect at the beginning and end of the cruise. The combined durations of C. finmarchicus (Gunnerus) stages CIII and CIV, calculated from the inverses of molting rates corrected for presence of diapausing C. glacialis Jaschnov, corresponded well with development times based on laboratory rearing experiments. We conclude that our molting rate measurements accurately reflected processes in nature. This methodology is useful for analyzing the dynamics and production of copepod populations.     

Population dynamics and production of the planktonic copepods in a eutrophic inlet of the Inland Sea of Japan. I. Centropages abdominalis

Population dynamics and production of the calanoid copepod Centropages abdominalis were studied from November 1986 to November 1987 in Fukuyama Harbor, in the central part of the Inland Sea of Japan. This species was present in the plankton during a cold-water period from November to June (temperature range: 8.9 to 21.1 °C), with a peak abundance (23 600 ind m^–3) in February. During this period, six generations could be detected, and each generation time agreed well with that predicted from food-satiated laboratory experiments, indicating that the natural population was not food-limited. The population suffered extremely high mortality during the period from egg to naupliar stage (N) II: only 0.02 to 4% of the eggs survived to NII. However, the mortality in stages older than NII was almost negligible. The growth rate of C. abdominalis increased exponentially with increasing temperature. Its biomass and production rate showed marked seasonal variations largely in parallel with numerical abundance. The estimated production between 7 November 1986 and 29 May 1987 was 355 mg C m^–3 or 2.66 g C m^–2, 95% of which occurred during February and March. The daily production rate to biomass ratio increased exponentially with temperature from 0.18 at 8.9°C to 0.37 at 19°C.     

Potential effect of phytoplankton colony breakage on the calculation of zooplankton filtration rates

Substantial net production of short chains of the diatom Skeletonema costatum occurred in grazing experiments conducted with Acartia hudsonica (=A. clausi). A general model was then constructed to evaluate the influence of colony breakage during grazing on the calculation of zooplankton filtration and ingestion rates. Breakage can lead to either over-or underestimation of these rates. The magnitude of error is related to breakage probability, particle size distribution, size of the largest colonies, length of the experiment, copepod concentration and actual filtration rates. Size distributions similar to those described in the literature as manifestations of a complex selection for size and particle abundance can be generated by the grazing model under conditions of a uniform filtration rate accompanied by colony breakage. Unless the rate of breakage exceeds the rate of removal and causes net particle production, the occurrence of breakage may go undetected.     

Ontogenetic feeding shifts in the meiobenthic harpacticoid copepod Nitocra lacustris

¹⁴C-radiolabelling experiments indicate that adult stages of the salt-marsh harpacticoid copepod Nitocra lacustris (Schmankevitsch) receive a large part of their nutrition through the ingestion and assimilation of certain diatoms. An abundance of empty diatom frustules occurs in the gutpellet contents of field-collected individuals. Naupliar stages do not ingest diatoms in the laboratory, and nauplii from the field do not contain frustules in their gut pellets. Ingestion of diatoms in the laboratory first occurs during the second or third copepodite stage. ³H-radiolabel expeiments and grazing experiments using bacterium-sized beads adhering to the diatoms indicated that both adults and nauplii ingest bacteria adhering to the outer mucus coating of the diatoms (and probably ingest the diatom mucus itself). Adults ingest bacteria (and probably mucus exopolymer) coincidently while ingesting diatoms. The nauplii ingest these components by scraping the outer surface of the diatoms. SEM observations indicate that diatoms are not punctured by the nauplii during feeding. While diatom mucus and associated bacteria play an (as yet unquantified) role in the nutrition of the adults, these components may comprise the bulk of food resources for naupliar stages.     

The influence of temperature and salinity on<Emphasis Type="Italic"> Acartia</Emphasis> (Copepoda: Calanoida) nauplii survival

Adult Acartia congeners, A. bifilosa, A. clausi, A. discaudata and A. tonsa, have distinct seasonal and spatial distribution patterns in Southampton Water (UK), reflecting patterns of temperature and salinity, respectively. The effect of these factors on other life stages, hatch success and naupliar survival was investigated by exposing the congeners to a range of salinity (15.5–33.3) and of temperature (5–20°C). A. clausi is known to prefer more saline waters, and showed highest hatch success at 33.3 salinity. A. tonsa is most tolerant to dilution, and at 15.5 salinity it had the highest hatch success of all the congeners. Hatch success in both A. bifilosa and A. discaudata was similar over the range of salinities investigated, confirming that they are intermediate species in terms of spatial distribution. The nauplii of all species survived well at the higher salinities and best at 33.3, which allows for differential transport of the poorly swimming nauplii to the mouth of the estuary until size and swimming ability increase, after which they can then return to regions of preferred salinity. The summer species, A. clausi and A. tonsa showed higher hatch success at 20°C, whereas A. discaudata, which is present in the water column all year round, showed no significant temperature-related differences in hatch success. A. bifilosa, which diapauses over summer, showed significantly higher hatch success at 10°C than at 20°C. The physiological relationship between temperature and development time was clear; naupliar survival of all species was highest at 20°C and all congeners reached the first copepodite stage (CI) significantly faster at 20°C. However, no consistent pattern was seen for salinity. It would appear that the adult Acartidae in Southampton Water remain in regions of their preferred salinity and lay eggs there which hatch well. However, because the nauplii are not good swimmers, they are swept towards the mouth of the estuary and into areas of higher salinity, where they remain and develop into more advanced stages before moving back up the estuary to take up their adult distribution pattern.Communicated by J.P. Thorpe, Port Erin     

Relationship between growth rate and egg production in the copepod Acartia clausi hudsonica

Egg production by Acartia clausi hudsonica ceases at low concentrations of Isochrysis galbana as food and at high levels reaches a maximum that increases with temperatures in the natural range. This increase parallels the rate of production of fecal pellets. Females without males can produce about 400 eggs before entering a generally short postreproductive period. Weight increments between copepodite stages are exponential and, assuming isochronal durations of stages and that development time of older stages is the same mutiple of embryonic duration at all temperatures, a temperature-dependent rate is estimated for pre-adult growth. We demonstrate that this growth rate also predicts the observed maximal rate of egg production by the nongrowing adult females. Published data for other copepod species (except Pseudocalanus) are inadequate for wider testing of this hypothesis, but available data do suggest that no such simple rule governs total output of eggs by females of different species.     

Life cycle of Pseudocalanus acuspes Giesbrecht (Copepoda, Calanoida) in the Central Baltic Sea: I. Seasonal and spatial distribution

The seasonal and spatial distribution of Pseudocalanus acuspes in the Bornholm Basin (Central Baltic Sea) was studied on 16 cruises between March 2002 and May 2003 from stratified (10 m) multinet samples. The highest abundances were reached in May 2002 and April 2003 (618×10³ and 869×10³ ind. m⁻², respectively). Ontogenetic vertical distribution was stage specific with differences of mean annual weighted mean depth >30 m between nauplii and males; it followed closely the hydrography which was characterized by a permanent halocline and a summer thermocline. The vertical distribution showed a positive correlation with salinity especially in the older developmental stages; the relationship to temperature was negative in the nauplii and copepodite stage I (CI). Most of the stages performed a seasonal migration. The consequences of the vertical distribution patterns in relation to the effects of climate and predation are discussed. A stage shift from nauplii in April/May to CIV and CV as overwintering stages indicated slow seasonal development. However, nauplii were observed all the year round, and the resulting stage structure did not allow to distinguish generations. Changes in the prosome length of females seemed to be related to the advection of water masses with different temperatures rather than to different generations. It could not be clarified whether the strong increase of nauplii and adults after an inflow event of cold, saline North Sea water in the beginning of 2003 was a result of advection or improvement in habitat conditions.     

Influence of cultivation and food concentration on body length of calanoid copepods

The cephalothorax length of the marine pelagic Copepoda Acartia clausi Giesbrecht, Temora longicornis (Müller), Centropages hamatus (Lilljeborg) and Pseudocalanus sp. was monitored at 15°C during prolonged cultivation through up to 55 filial generations and at different concentrations of food. The length of T. longicornis decreased considerably during the first 15 generations and remained rather constant thereafter. In the other species, body length increased slightly or remained almost constant. Genetic changes are probably involved. Food concentration influenced body size of all species, particularly C. hamatus, in which 80% of the natural size range may be explained by differences in food concentration. The idea that temperature is a dominant factor in determining the length of copepods should be reconsidered.     

Population dynamics and production of the planktonic copepods in a eutrophic inlet of the Inland Sea of Japan. IV. Pseudodiaptomus marinus, the egg-carrying calanoid

Population dynamics and production of the egg-carrying calanoid copepod Pseudodiaptomus marinus were studied for a year in Fukuyama Harbor, a eutrophic inlet of the Inland Sea of Japan. This species was perennial, with a large numerical peak in June and small peaks in September/October and November/December. During the study period, at least 11 generations could be detected. For each generation, the stage-specific survival from egg to Copepodite Stage (C) V was determined; it was very high during early life stages (egg to NIII), and gradually decreased beyond. On average, 94% of eggs recruited into NIII, which is strongly contrasted with very high (>ca. 90%) mortality during the corresponding stages for free-spawning copepods, i.e. Acartia omorii, Centropages abdominalis and Paracalans sp. This demonstrates that the egg-carrying strategy has a great advantage to reduce mortality in egg stage. The biomass of this species showed marked seasonal variations largely in parallel with numerical abundance. The instantaneous somatic growth rate increased linearly with temperature. The population production rate was estimated as the sum of somatic growth of larval stages and egg production of adult females; the annual integration was 51.0 mg C m⁻³ yr⁻¹ or 0.38 g C m⁻² yr⁻¹. Received: 11 November 1996 / Accepted: 7 December 1996