Abundance,growth and grazing loss rates of picophytoplankton in Barguzin Bay,Lake Baikal

The abundance, growth, and grazing loss rates of picophytoplankton were investigated in August 2002 in Barguzin Bay, Lake Baikal. Water samples for incubation were taken once at a near-shore station and twice at an offshore station. Contributions of picophytoplankton to total phytoplankton were high (56.9–83.9%) at the offshore station and low (5.8–6.8%) at the near-shore station. The picophytoplankton community in the offshore station comprised mainly phycoerythrin (PE)-rich cyanobacteria, with eukaryotic picophytoplankton being less abundant. In contrast, as well as PE-rich cyanobacteria and eukaryotic picophytoplankton, phycocyanin (PC)-rich cyanobacteria were found in the near-shore station. At the offshore station, growth and grazing loss rates on 25 August were 0.56 and 0.43 day⁻¹, respectively, and on 29 August, 0.69 and 0.83 day⁻¹, respectively. At the near-shore station, growth and grazing loss rates were 1.61 and 0.70 day⁻¹, respectively. These results show that there is a difference in the abundance, composition, and ecological role in the microbial food web of picophytoplankton between the near-shore and the offshore areas in Barguzin Bay.     

Structure and seasonal trophodynamics of picophytoplankton in sevastopol bay and adjacent waters (the Black Sea)

Abundance and seasonal trophodynamics (specific growth rate, daily production, and grazing mortality) of the major picophytoplankton components, Synechococcus cyanobacteria (Syn) and picoeukaryotes (Pico-E), were studied at three stations in Sevastopol Bay and adjacent coastal waters (the Black Sea) in 2014 by flow cytometry and the dilution method. Pico-E abundance was shown to increase along the nutrient and pollution gradient from the coastal waters outside the bay (annual average of 7.3 ± 5.4 × 10³ cells mL^–1) to the eastern corner of the bay (28.7 ± 11.4 × 10³ cells mL^–1), while no relation was found between the water pollution status and Syn abundance (9.9 ± 8.7 × 10³ cells mL^–1; at all the stations, n = 27). Matter flows through the communities (daily production for Syn and Pico-E 0^–16.6 and 0^–19.3 µg C L^–1 day^–1, respectively; grazing mortality for Syn and PicoE 0–3.6 and 0–21.2 µg C L^–1 day^–1, respectively) were comparable to or even exceeded their biomass stocks (>0.05–6.8 and 0.9–26.5 µg C L^–1 for Syn and PicoE, respectively), indicating high biomass turnover rates. The highest flow-to-stock ratio (up to 6 for Syn) and a significant imbalance between daily production (P) and grazing mortality (G) were observed in the most polluted and eutrophic waters of the bay in spring (Pico-E: P/G < 1) and late summer (Syn: P/G > 1). Black River inflow to the bay was hypothesized to be among the mechanisms maintaining this pronounced and long-term imbalance in the open system without any negative consequences for the picophytoplankton assemblages.     

三门湾浮游动物的季节变动及微型浮游动物摄食影响

2002年8月、11月、2003年2月和5月,在三门湾进行了4个航次生物、化学和水文等专业综合调查。根据采集的浮游动物样品的分析鉴定及海上现场实验结果,对浮游动物的群落组成、生物量、丰度、多样性指数的分布和季节变动及其浮游动物对浮游植物的摄食影响进行研究。结果表明,三门湾浮游动物有67属,89种,16类浮游幼体,主要可划分为4个生态类群：以近岸低盐类群为主,其优势种为中华哲水蚤Calanus sinicus、真刺唇角水蚤Labidocera etwhaeta、捷氏歪水蚤Tortanus derjugini、太平洋纺锤水蚤Acartiapacifica、中华假磷虾Pseudeuphausia sinica和百陶箭虫Sagitta bedoti等。半咸水河口类群、暖水性外海类群和广布种相对较少。浮游动物生物量和丰度的平面分布趋势除了夏季有所差异外,其它季节基本一致。2月份和5月份,浮游动物生物量和丰度,从湾顶向湾口呈逐渐增加趋势;8月份,湾口区生物量最高,而丰度高值区出现在湾顶部;11月份,生物量和丰度的平面分布相对均匀。浮游动物种类多样性指数有明显的季节变化,其动态变化与浮游动物种数和丰度的变化一致。微型浮游动物对浮游植物存在摄食压力,且有季节变化,摄食率的变化在0．18．0．68d^-1,微型浮游动物的摄食率低于相同季节的浮游植物生长率。微型浮游动物对浮游植物摄食压力的变化范围为16．1％-49．1％d^-1,对初级生产力摄食压力的变化在58．3％-83．6％d^-1。11月份,微型浮游动物对浮游植物和初级生产力的摄食压力均出现最高值。     

Application of the size-fractionation method to simultaneous estimation of clearance rates by heterotrophic flagellates and ciliates of pico- and nanophytoplankton

To estimate the clearance rates of pico- and nanophytoplankton by heterotrophic nanoflagellates (HNF) and ciliates, the size-fractionation method was employed in combination with a multiple regression analysis. Apparent growth rate of a specific phytoplankton group was decomposed into three terms, net growth rate, grazing rates by HNF and those by ciliates, and the grazing rates were interpreted as a linear function of average cell concentrations of HNF and ciliates. We produced a set of subsamples from a water sample by size-fractionation using three different pore sizes. By measuring phytoplankton and protozoan cell concentrations, apparent growth rate of a specific phytoplankton group was regressed against the average cell concentrations of HNF and ciliates to obtain the net growth rate of the phytoplankton group and the average clearance rates by these two protozoan groups. The estimated values were within the range of those previously reported for cultured and natural protozoan, which supported the feasibility of the present method. The estimated values also suggested that picophytoplankton abundance in Otsuchi Bay in spring is controlled mainly by HNF through active grazing. The present study rediscovered the utility of the size-fractionation method as a method to estimate the clearance rates of different protozoan groups from natural assemblages in a single experiment.     

Impact of Water Column Acidification on Protozoan Bacterivory at the Lake Sediment-Water Interface

Although the impact of acidification on planktonic grazer food webs has been extensively studied, little is known about microbial food webs either in the water column or in the sediments. Protozoon-bacterium interactions were investigated in a chronically acidified (acid mine drainage) portion of a lake in Virginia. We determined the distribution, abundance, apparent specific grazing rate, and growth rate of protozoa over a pH range of 3.6 to 6.5. Protozoan abundance was lower at the most acidified site, while abundance, in general, was high compared with other systems. Specific grazing rates were uncorrelated with pH and ranged between 0.02 and 0.23 h^-1, values similar to those in unacidified systems. The protozoan community from an acidified station was not better adapted (P = 0.95) to low-pH conditions than a community from an unacidified site (multivariate analysis of variance on growth rates for each community incubated at pHs 4, 5, and 6). Both communities had significantly lower (P < 0.05) growth rates at pHs 4 and 5 than at pH 6. Reduced protozoan growth rates coupled with high grazing rates and relatively higher bacterial yields (ratio of bacterial-protozoan standing stock) at low pH indicate reduced net protozoan growth efficiency and a metabolic cost of acidification to the protozoan community. However, the presence of an abundant, neutrophilic protozoan community and high bacterial grazing rates indicates that acidification of Lake Anna has not inhibited the bacterium-protozoon link of the sediment microbial food web.     

Demographic,mechanistic and density-dependent determinants of population growth rate: a case study in an avian predator

Identifying the determinants of population growth rate is a central topic in population ecology. Three approaches (demographic, mechanistic and density-dependent) used historically to describe the determinants of population growth rate are here compared and combined for an avian predator, the barn owl (Tyto alba). The owl population remained approximately stable (r approximately 0) throughout the period from 1979 to 1991. There was no evidence of density dependence as assessed by goodness of fit to logistic population growth. The finite (lambda) and instantaneous (r) population growth rates were significantly positively related to food (field vole) availability. The demographic rates, annual adult mortality, juvenile mortality and annual fecundity were reported to be correlated with vole abundance. The best fit (R(2) = 0.82) numerical response of the owl population described a positive effect of food (field voles) and a negative additive effect of owl abundance on r. The numerical response of the barn owl population to food availability was estimated from both census and demographic data, with very similar results. Our analysis shows how the demographic and mechanistic determinants of population growth rate are linked; food availability determines demographic rates, and demographic rates determine population growth rate. The effects of food availability on population growth rate are modified by predator abundance.     

Fast microzooplankton grazing on fast-growing,low-biomass phytoplankton: a case study in spring in Chesapeake Bay,Delaware Inland Bays and Delaware Bay

Dilution experiments were performed to examine the growth and grazing mortality rates of picophytoplankton (<2 μm), nanophytoplankton (2–20 μm), and microphytoplankton (>20 μm) at stations in the Chesapeake Bay (CB), the Delaware Inland Bays (DIB) and the Delaware Bay (DB), in early spring 2005. At station CB microphytoplankton, including chain-forming diatoms were dominant, and the microzooplankton assemblage was mainly composed of the tintinnid Tintinnopsis beroidea. At station DIB, the dominant species were microphytoplanktonic dinoflagellates, while the microzooplankton community was mainly composed of copepod nauplii and the oligotrich ciliate Strombidium sp. At station DB, nanophytoplankton were dominant components, and Strombidium and Tintinnopsis beroidea were the co-dominant microzooplankton. The growth rate and grazing mortality rate were 0.13–3.43 and 0.09–1.92 d⁻¹ for the different size fractionated phytoplankton. The microzooplankton ingested 73, 171, and 49% of standing stocks, and 95, 70, and 48% of potential primary productivity for total phytoplankton at station CB, DIB, and DB respectively. The carbon flux for total phytoplankton consumed by microzooplankton was 1224.11, 100.76, and 85.85 μg C l⁻¹ d⁻¹ at station CB, DIB, and DB, respectively. According to the grazing mortality rate, carbon consumption rate and carbon flux turn over rates, microzooplankton in study area mostly preferred to graze on picophytoplankton, which was faster growing but was lowest biomass component of the phytoplankton. The faster grazing on Fast-Growing-Low-Biomass (FGLB) phenomenon in coastal regions is explained as a resource partitioning strategy. This quite likely argues that although microzooplankton grazes strongly on phytoplankton in these regions, these microzooplankton grazers are passive. Handling editor: K. Martens     

Effects of herbivory, nutrient levels, and introduced algae on the distribution and abundance of the invasive macroalga Dictyosphaeria cavernosa in Kaneohe Bay, Hawaii

Since the 1960s, and possibly earlier, the macroalga Dictyosphaeria cavernosa has overgrown and displaced corals on reef slopes and outer reef flats in Kaneohe Bay, Oahu. This shift in reef community composition is generally attributed to nutrient enrichment resulting from sewage discharge. Following the diversion of most of the sewage effluent in 1977-1978, it was expected that D. cavernosa growth would become nutrient-limited and its abundance would consequently decline, but the alga remains abundant in much of the bay. One explanation for its persistence is that nutrients are once again high enough to support the alga's growth. An alternative explanation is that there has been a reduction in grazing intensity in the bay. In this study we resurveyed the distribution and abundance of D. cavernosa at 120 reef slope sites originally surveyed in 1969. We conducted additional surveys to estimate the biomass of herbivores and the areal coverage of D. cavernosa and other macroalgae on reef slopes and flats. Field experiments were used to determine spatial and temporal patterns of grazing intensity on and growth rates of D. cavernosa and the introduced macroalga Acanthophora spicifera. Laboratory experiments were used to examine preferences among herbivores for some of the most abundant macroalgae on Kaneohe Bay reefs. Twenty years after sewage diversion, D. cavernosa cover on reef slopes has decreased substantially in southern Kaneohe Bay, the site of most of the historical sewage discharge. D. cavernosa cover has changed less in other regions, remaining high in the central bay and low in the north bay. D. cavernosa thalli protected by grazer exclusion cages sustained positive growth rates on reef slopes and flats throughout the bay. Reduced nutrient concentrations may have caused a reduction in D. cavernosa growth rates, and a consequent reduction in D. cavernosa abundance in the south bay shortly after sewage diversion. Measurements of grazing intensity and surveys of herbivorous fish abundance suggest that the continued abundance of D. cavernosa is the result of a reduction in grazing intensity. Reduced grazing intensity on D. cavernosa may in turn be the result of a historical reduction in herbivore biomass or the establishment of several introduced macroalgae on reef flats. The introduced species are preferred by herbivorous fishes over D. cavernosa, as indicated by preference tests. The hypothesis that reduced grazing pressure on D. cavernosa is related to the establishment of introduced species is supported by the observation that D. cavernosa cover is highest on reef slopes where the cover of preferred introduced macroalgae on the adjacent outer reef flat is also high. Conversely, D. cavernosa cover is low or zero on reef slopes where the cover of introduced macroalgae on the adjacent reef flat is low or zero     

Biochemical composition of crustacean zooplankton and their grazing on phytoplankton and ciliated protozoans in a recently founded reservoir (Sahela, Morocco

In order to assess the impact of crustacean zooplankton on phytoplankton and protozoan ciliates in the Sahela reservoir under semi-arid climate, we conducted experiments during the period from July to December 1999 at the deepest point in the lake (15 m). Samplings and measurements were carried out in diffusion chambers submerged in situ over a period of 7 h without (control chambers) and with (experimental chambers) crustacean zooplankton. During these experiments, counts were conducted on phytoplankton and ciliates to determine the abundance and the mortality of these organisms due to zooplankton in each diffusion chambers at t = 0 and t = 7 h of incubation. The study showed that the growth rates of phytoplankton and ciliates populations varied between 0.02 and 0.05 h-1 and from 0.01 to 0.07 h-1, respectively. The mortality caused by zooplankton grazing fluctuated from 0.07 to 0.2 h-1 of phytoplankton and from 0.01 to 0.2 h-1 of ciliates. These mortalities were significantly and positively correlated with the growth rates (r = 0.8; p < 0.02; n = 9). Moreover, the heavy predation by the crustacean zooplankton was exerted on small-sized phytoplankton and ciliates and we demonstrated the relationships between protozoans and zooplankton for the transfer of matter and energy in aquatic food webs. Furthermore, the crustacean zooplankton metabolism was different, whether zooplankton was present in diffusion chambers or in the lake.     

Food supply, grazing activity and growth rate in the limpet Patella vulgata L.: a comparison between exposed and sheltered shores

The limpet Patella vulgata L. is an important microphagous grazer on intertidal rocky shores of north-west Europe, occurring across the wave exposure gradient. Groups of P. vulgata were selected at mid-tide level of two exposed shores and two sheltered, fucoid dominated shores on the Isle of Man, British Isles, and manipulated to equivalent densities and population structure. The level of grazing activity and growth rate were determined over a 1-year period. At the same time, the abundance of epilithic microalgae, measured as the concentration of chlorophyll a, was determined as an estimate of food supply. Microagal abundance showed a seasonal pattern in both exposed and sheltered conditions, with higher levels in winter compared to summer. In both seasons, the microalgal resource was more abundant on the sheltered shore studied. The level of grazing activity in P. vulgata showed a seasonal pattern on the exposed but not the sheltered shores. Averaged over the year, grazing activity on the exposed shores was over double that on sheltered shores. Thus, in sheltered conditions, food supply for limpets was high and grazing activity low; in exposed conditions, food supply was low and grazing activity high. The growth rate of P. vulgata, measured as increase in shell length, showed no significant difference between exposed and sheltered shores. Growth rate was also determined in P. vulgata at natural densities. Although the overall density declined with decreasing exposure to wave action, the density per unit area of grazeable substance was higher in shelter. In these populations, the mean growth rate was over twice as high on exposed compared to sheltered shores.     

Hatch-period-dependent early growth and survival of Pacific herring Clupea pallasii in Miyako Bay, Japan

Considerable interannual variation in the abundance of larval and juvenile Pacific herring Clupea pallasii was detected in Miyako Bay, on the Pacific coast of northern Japan; abundances were high in 2001 and 2003 and low in 2000 and 2002. Hatch dates and growth rates for larval and juvenile survivors were estimated through otolith analysis. Water temperature and food availability were monitored on the spawning and nursery grounds in the inner part of the bay. The number of spawning females caught in nets set around the spawning ground was recorded during each spawning season (January to May) in 2000–2003. No correlation was found between the number of spawning females and the abundance of larvae and juveniles on the spawning and nursery grounds. The hatch dates of surviving larvae and juveniles were concentrated at the end of the spawning season in 2001 and in the middle of the season in 2003. The larvae experienced relatively high prey concentrations during the first-feeding period in 2001 but low concentrations in 2003. Survival of larvae during the first-feeding period may be a function of prey concentration as well as water temperature. In 2003, low water temperature would reduce starvation mortality during the first-feeding period. In contrast, unfavourable feeding conditions with higher temperatures during the first-feeding period seemed to result in low larval survival in 2000 and 2002. The 2001 larvae grew faster than those in 2003 because of the late hatch dates and the higher ambient temperatures that resulted. Temperature might be a major factor controlling growth rates of C. pallasii larvae in Miyako Bay.     

Photo- and heterotrophic pico- and nanoplankton in the Mississippi River plume: distribution and grazing activity

The abundance of pico- and nanophytoplankton, bacteria and heterotrophicnanoflagellates, and grazing rates on phototrophic pico- andnanoplankton and bacterioplankton were assessed along a salinitygradient (0.2–34.4) in the Mississippi River plume inMay 2000. Grazing rates were established by serial dilutionexperiments, and analysis by flow cytometry allowed differentiationof grazing rates for different phytoplankton subpopulations(eukaryotes, Synechococcus spp., Prochlorococcus spp.). Grazingrates on phytoplankton tended to increase along the salinitygradient and often approached or exceeded 1 day^-1. Phytoplanktonnet growth rates (growth – grazing) were mostly negative,except for positive values for eukaryotic nanoplankton in thelow-salinity, high-chlorophyll region. Grazing pressure on bacteriawas moderate (     

Long-term and seasonal dynamics of the recruitment and growth of youngBalanus rostratus barnacles in Amurskii Bay, Sea of Japan

The changes in distribution and abundance of the barnacleBalanus rostranus that occurred at various sites of Amurskii Bay in 1982–1995 were studied. Increased water and sediment pollution by industrial and sewage discharge were found to most significantly affect the abundance of larvae, food composition, and the availability of substrata suitable for larva to settle. The mortality of young barnacles increased and the growth rate decreased in the most polluted areas of the bay at water temperatures higher than 18°C and at critically low oxygen saturation.     

Microbial herbivory on the brown tide alga, Aureococcus anophagefferens: results from natural ecosystems, mesocosms and laboratory experiments

Experiments were conducted with natural plankton assemblages from two areas in Great South Bay (GSB) and the Peconic Bays Estuary System, NY, to compare the rates of growth and pelagic grazing mortality of Aureococcus anophagefferens with co-occurring phytoplankton. We hypothesized that A. anophagefferens would experience low mortality rates by microbial herbivores (relative to feeding pressure on other algae) thus providing it with a competitive advantage within the phytoplankton community. In fact, substantial rates of mortality were observed in nearly every experiment in our study. However, mortality rates of A. anophagefferens were less than intrinsic growth rates of the alga during late spring and early summer in Great South Bay, resulting in positive net growth rates for the alga during that period. This timing coincided with the development of a brown tide in this estuary. Similarly, growth rates of the alga also exceeded mortality rates during bloom development in natural plankton assemblages from the Peconic Bays Estuary System held in mesocosms. In contrast to the situation for A. anophagefferens, growth rates of the total phytoplankton assemblage, and another common picoplanktonic phytoplankter (Synechococcus spp.), were frequently less than their respective mortality rates. Mortality rates of A. anophagefferens in both systems were similar to growth rates of the alga during later stages of the bloom. Laboratory studies confirmed that species of phagotrophic protists that consume A. anophagefferens (at least in culture) are present during brown tides but preference for or against the alga appears to be species-specific among phagotrophic protists. We conclude that two scenarios may explain our results: (1) protistan species capable of consuming the brown tide alga were present at low abundances during bloom initiation and thus not able to respond rapidly to increases in the intrinsic growth rate of the alga, or (2) the brown tide alga produced substance(s) that inhibited or retarded protistan grazing activities during the period of bloom initiation. The latter scenario seems less likely given that significant mortality of A. anophagefferens was measured during our field study and mesocosm experiment. However, even a minor reduction in mortality rate due to feeding selectivity among herbivores might result in a mismatch between growth and grazing of A. anophagefferens that could give rise to significant net population growth of this HAB species. Either scenario infers an important role for trophic interactions within the plankton as a factor explaining the development of brown tides in natural ecosystems.     

Microzooplankton grazing and the control of phytoplankton biomass in the Suwannee River estuary,USA

Microzooplankton grazing can have significant impacts on the distribution and abundance of phytoplankton, thereby influencing the frequency and duration of algae blooms. Observations of high ciliate abundances in the Suwannee River estuary, Florida, suggest a significant potential for top-down pressure on the phytoplankton community by microzooplankton. We examined the composition of the microzooplankton and determined grazing mortality losses for phytoplankton within the Suwannee River estuary from 2001 to 2002. Our results indicated grazing mortality rates of 1.4 d⁻¹, equivalent to a loss of up to 76% of phytoplankton standing crop and up to 83% of total daily primary production. The microzooplankton community was primarily composed of ciliates, dinoflagellates, and copepod nauplii. The densities of ciliates in the estuary were comparable to densities reported in highly eutrophic ecosystems (9,400–72,800 ciliates l⁻¹). Grazing pressure on small phytoplankton may be further enhanced because ciliates and small dinoflagellates have growth rates similar to those of phytoplankton, and therefore can keep up with surges in abundance. Handling editor: Judit Padisak     

Seasonal dynamics and grazing rate of zooplankton in Yueqing Bay,China

The species composition,biomass,abundance,and species diversity of zooplankton were determined for samples collected from August 2002 to May 2003 from 14 stations in Yueqing Bay,China.Phytoplankton growth rate and microzooplankton grazing rate were obtained by using the dilution method developed by Landry and Hassett.The spatial and temporal variations of zooplankton and its relationship with environmental factors were also analyzed.The results showed that the zooplankton in the Yueqing Bay could be divided into four ecotypes,namely coastal low saline species,estuary brackish water species,offshore warm water species,and eurytopic species.A total of 75 species of zooplankton belonging to 56 genera and 17 groups of pelagic larva were identified in the Yueqing Bay.The coastal low saline species was the dominant ecotype in the study area,and the dominant species were Labidocera euchaeta,Acartia pacifica,Acrocalanus gibber,Pseudeuphausia sinica,and Sagitta bedoti among others.There was considerable seasonal variation in zooplankton biomass and abundance in the surveyed areas.The peak biomass appeared in August,descending in November and in May,and the lowest biomass appeared in February.Similarly,the highest abundance of zooplankton was observed in August,with the abundance descending in the following months:May,November,and February.There were similar horizontal distribution patterns for the biomass and the abundance of zooplankton.They both increased from the upper to the lower bay in February and May,but decreased from the upper to the lower bay in August.Biomass and abundance were evenly distributed in the Yueqing Bay in November.Moreover,there was marked seasonal variation in the species diversity of zooplankton,which conformed to the abundance of zooplankton.Results of the dilution experiments indicated that there was grazing pressure of microzooplankton on phytoplankton in the Yueqing Bay throughout the year though the rate of microzooplankton grazing on phytoplankton varied seasonally.Phytoplanktons were growing at 0.26-2.07/d and grazed by microzooplankton at a rate of 0.15--0.48/d in different seasons.     

夏季胶州湾微型浮游动物摄食初步研究

2002年6月至7月间对胶州湾内、外和港口3个典型站位进行了微型浮游动物对浮游植物的摄食研究．按陆基半现场方式进行了4次稀释法实验,对湾外相同的站位进行了两次实验,对湾内和港口各进行了一次实验,获取了研究站位浮游植物和微型浮游动物种类、丰度、体积转换浮游植物碳含量、碳／叶绿素比率、浮游植物净生长率、微型浮游动物摄食率、对潜在初级生产力的摄食压力、对浮游植物现存量的摄食压力以及碳摄食通量等参数．湾外和湾内站位的浮游植物组成相似,优势种为新月柱鞘藻(Cylindrotheca closterium)和中肋骨条藻(Skeletonema costatum),港口浮游植物优势种类为中肋骨条藻、浮动湾角藻(Eucampia zodiacus)和旋链角毛藻(Chaetoceros curvisetus)．湾外微型浮游动物的优势种为百乐拟铃虫(Tintinnopsis beroidea),而在湾内为百乐拟铃虫和急游虫(Strombidium sp．),港口主要为急游虫,也有少数的百乐拟铃虫．微型浮游动物对浮游植物的摄食率和对潜在初级生产力的摄食压力,在湾内最高,其次在湾外,港口最低．微型浮游动物对浮游植物的摄食率,在湾外,分别为0．96和1．20d^-1,在湾内为1．33d^-1,在港口为0．36d^-1．微型浮游动物对潜在初级生产力的摄食压力,在湾外,分别为74％和84％,在湾内为93％,在港口为53％．微型浮游动物的碳摄食通量在港口最高达到281mgC·m^-3·d^-1,在湾内为102mgC·m^-3·d^-1,在湾外最低范围在31～49mgC·m^-3·d^-1．浮游植物的细胞大小和两种微型浮游动物的摄食习性的不同是造成研究站位微型浮游动物摄食率和摄食压力不同的主要原因．同世界其它内湾相比,胶州湾微型浮游动物的摄食压力处于中等水平。     

Spatial and Temporal Variability in Juvenile Pacific Herring, Clupea pallasi, Growth in Prince William Sound, Alaska

We examined the spatial and temporal variability of juvenile Pacific herring, Clupea pallasi, growth within Prince William Sound, Alaska. Pacific herring, ranging from post-larval to mature fish, were collected from four spatially segregated bays between October 1995 and March 1998. Linear growth equations from each bay were similar. However, growth rates and wet weight-at-length, reflecting condition, of juvenile Pacific herring cohorts varied seasonally and annually. The short term spatial variability in juvenile Pacific herring growth suggested that each bay was a unique nursery area. The physical and biological conditions within each bay appeared to dictate Pacific herring growth rate.     

Relationships between heterotrophic nanoflagellates and the demographic response of Daphnia longispina in a eutrophic lake with poor food quality conditions

1. Based on both field data and laboratory studies, the summer population of Daphnia longispina living in a stratified eutrophic lake was examined in relation to the abundance of algae, nanoflagellates and picocyanobacteria.
2. In early July, the Daphnia population replaced Bosmina and remained the dominant zooplankter during summer 1994. Its development in July was concomitant with an increase of edible algae but, despite the apparent abundance in available food, the Daphnia population decreased throughout August suggesting poor food conditions.
3. From mid-August to the beginning of September, the biomass of inedible phytoplankton was greater than that of the smaller, edible fraction. Consequently the average rate of increase, birth rates and fecundity of Daphnia remained low. Although the biomass of heterotrophic nanoflagellates was consistently low, the demographic parameters of Daphnia were correlated throughout this period with these protozoans.
4. Life table experiments run in the laboratory showed that epilimnetic food supported both the growth in length of individual Daphnia and an increase in fecundity, but metalimnetic food supported only individual growth. D. longispina probably failed to reproduce because of the abundance of detritus mixed with the heterotrophic nanoflagellates in the metalimnetic water at that period of the year. The vertical migration of Daphnia into these deeper layers could be caused by a predator avoidance mechanism.     

Compensation in individual growth rates and its influence on lake trout population dynamics in the Michigan waters of Lake Superior

The role of compensatory mechanisms in the population dynamics of lake trout in the Michigan waters of Lake Superior was explored during three time periods: the pre-sea lamprey period, prior to 1950 when lake trout were at a relatively high abundance and the fishery was the primary source of lake trout mortality; the sea lamprey dominant period, from 1951 to 1961 when lake trout were at a very low abundance due to sea lamprey predation and overexploitation; and currently, from 1985 to 1993 when wild lake trout abundance was at a moderate level. The role of compensatory changes in growth and fecundity rates of lake trout in the Michigan waters of Lake Superior was evaluated using a life table approach. Individual growth and fecundity rates were calculated and compared between time periods. These rates were used to determine age-specific fecundity which, along with age-specific survival, were incorporated into a Leslie projection matrix to calculate the finite rate of population increase (λ). Individual growth rates and age-specific fecundity rates changed in response to the different levels of lake trout abundance during each of the study periods. Lake trout during the sea lamprey dominant period, which experienced the lowest abundance and highest mortality levels, exhibited the fastest individual growth rates and the highest age-specific fecundity. These high rates contributed to the relatively large compensatory scope exhibited by lake trout during the sea lamprey dominant period as compared to lake trout during the pre-sea lamprey or the current periods which are associated with higher levels of abundance.