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1.
2009年1月在南海北部海域的5个站位,采用稀释法和显微分析技术研究了浮游植物生长率及微型浮游动物对浮游植物的摄食压力,同时测定了微型浮游动物的丰度及类群组成.结果表明:南海北部微型浮游动物类群主要以无壳纤毛虫为主,南海北部微型浮游动物类群细胞丰度为33~529个/dm3.南海北部浮游植物生长率为0.45~1.83 d-1,微型浮游动物摄食率为0.44~1.76 d-1,摄食压力占浮游植物现存量的42.6%~82.8%,占初级生产力的97.3%~225.1%.近岸区摄食压力比陆架区高,表明冬季南海近岸区微型浮游动物摄食能够有效的控制浮游植物的生长,而陆架区浮游植物生长率大于摄食率,浮游植物存在着现存量的积累,微型浮游动物并不能完全控制浮游植物的生长.  相似文献   

2.
2004年7~8月在台湾海峡南部的5个站位,用稀释法研究了浮游植物的生长率,微型浮游动物对浮游植物的摄食率及其生产力.微型浮游动物主要为无壳纤毛虫,尤其是急游虫类和侠盗虫类.浮游植物的生长率为0.52~0.72/d,浮游动物的摄食率为0.45~1.33/d,相当于每天摄食浮游植物现存量的36%~74%和初级生产力的88%~141%.微型浮游动物的次级生产力(MP02)为初级生产力的28.5%~58.4%.表明微型浮游动物在台湾海峡夏季海洋生态系统的能量流动中发挥着重要的作用.  相似文献   

3.
根据2005年8月和11月的调查资料,利用现场稀释法,以叶绿素a为检测对象,分别对三亚湾海区夏秋两季微型浮游动物的摄食情况进行研究。结果表明,夏秋两季浮游植物瞬时生长率(k)分别为0.9~1.32/d和1.81~3.30/d,而微型浮游动物的摄食率(g)则为0.85~1.79/d和1.29~2.57/d。对浮游植物现存量和初级生产力的摄食压力分别是,夏季为57.26%~83.30%和78.13%~140.38%,秋季为72.47%~92.35%和86.65%~97.90%。秋季微型浮游动物以微型浮游植物为其主要食物来源,其摄食率和对初级生产力的摄食压力最高,平均分别为1.09/d和107.98%;微型浮游植物的瞬时生长率也是最高的,平均为0.94/d,为浮游植物群体的主要组成部分。在三亚湾夏秋两季可把微型浮游动物作为控制浮游植物生长的重要影响因子之一,同时与秋季相比,夏季微型浮游动物在物质循环和能量流动方面起到更显著的作用。  相似文献   

4.
三亚湾珊瑚礁海区微型浮游动物种群组成和摄食研究   总被引:2,自引:0,他引:2  
采用现场稀释法,以叶绿素 a 为检测对象,利用 2006 年 4 月的调查资料对三亚湾珊瑚礁海区微型浮游动物的种群组成和摄食情况进行了研究.结果表明,区内微型浮游动物的组成以纤毛虫为主.微型浮游动物以 Tintinnopsis compressa, Tintinnopsis cylindrical, Tintinnidium semicilidium 三种纤毛虫为优势种,其中 Tintinnopsis 属纤毛虫是优势种群,有 38 种,占总纤毛虫种数的37.3 %.微型浮游动物的摄食率 ( g ) 在 1.28 ~ 2.37 d-1之间,平均值为 0.945 d-1;浮游植物瞬时增长率 ( k ) 为 0.26 ~ 1.44 d-1,平均值为 1.963 d-1;微型浮游动物对浮游植物现存量和初级生产力的摄食压力分别在 72.20 % ~90.65 % 和 113.31 % ~ 315.34 %,平均值分别为 84.56 % 和 177.05 %.三亚湾珊瑚礁海区内,微型浮游动物的摄食水平主要取决于水体中微型浮游动物和叶绿素a之间的相对数量关系.在控制浮游植物生长和转移浮游植物生产力方面微型浮游动物起着相当重要的作用,可以在一定程度上降低潜在的富营养化威胁.  相似文献   

5.
通过对山东省靖海湾海蜇养殖港塭定期采样,采用稀释法研究该海蜇养殖港塭水体中浮游植物的生长率、微型浮游动物对浮游植物的摄食率、摄食压力以及微型浮游动物的生产力。研究结果表明,海蜇养殖港塭微型浮游动物组成比较简单,海蜇养殖期间微型浮游动物丰度低于海蜇捕捞结束期。其中,海蜇养殖期间微型浮游动物的优势种为根状拟铃虫(Tintinnopsis radix),为600~2 600 ind/L,而海蜇捕捞结束后优势种为根状拟铃虫、诺氏麻铃虫(Leprotintinnus nordquisti)和运动类铃虫(Codonellopsis mobilis),丰度分别为3 000~6 000、1 500~3 0001、500~3 000 ind/L。研究期间,该港塭浮游植物生长率为0.05~1.03 d-1。微型浮游动物的摄食率为0.24~2.37 d-1,对浮游植物现存量的摄食压力为21.10%~90.61%,对潜在初级生产力的摄食压力为77.08%~583.68%,而微型浮游动物的次级生产力占初级生产力的22.92%~76.92%。本研究表明微型浮游动物在海蜇养殖港塭生态系统物质和能量流动中起着重要作用。  相似文献   

6.
南极普里兹湾边缘浮冰区微型浮游动物的摄食及其氮的排泄   总被引:14,自引:1,他引:13  
于1998–1999年夏季在南极普里兹湾边缘浮冰区利用稀释培养实验进行了微型浮游动物对浮游植物的摄食现场实验研究,同时对微型浮游动物的氨氮产生率进行了推算。结果表明,微型浮游动物的日摄食量为5.1–25.0mgC/(m3*d),占浮游植物现存量的10%–65%,对初级生产力的摄食压力也较大(34%–100%)。利用微型浮游动物的摄食率推算得出其氮产生率为0.44–1.75mg/(m3*d),达到维持现场初级生产所需氨氮的68%–536%。由此可见,微型浮游动物在南极夏季边缘浮冰区海洋生态系统中,特别是对浮游植物的生产和归宿起着十分重要的调控作用。  相似文献   

7.
于2005年3月对黄海海域的7个站位应用稀释法研究了浮游植物的生长率和微型浮游动物对浮游植物的摄食压力。结果表明:实验期间,微型浮游动物生长速率范围在0.34~0.95d-1,浮游植物摄食速率范围在0.44~0.94d-1。微型浮游动物对浮游植物的现存量和初级生产力的摄食压力分别为47.76%~63.80%和61.50...  相似文献   

8.
厦门杏林虾池夏冬季微型浮游动物对浮游植物的摄食压力   总被引:11,自引:0,他引:11  
20 0 0年 8月和 2 0 0 1年 2月 ,在杏林虾池用稀释法研究了微型浮游动物对浮游植物的摄食压力 .结果表明 :砂壳纤毛虫、甲壳类无节幼体是微型浮游动物的优势种 ;浮游植物生长率夏季为 0 .40~ 1 .0 1 /d、冬季为 0 .1 8~ 0 .96/d ;浮游动物的摄食率夏季为 0 .578~ 1 .3 2 4/d、冬季为 0 .2 0 4~ 0 .2 55/d ;日摄食率 (以C计 )夏季为 1 9.1 7~89.51mg/(m3·d)、冬季为 3 .3 2~ 7.2 3mg/(m3·d) ,各占浮游植物现存量的 43 .90 %~ 73 .40 %、1 8.43 %~ 2 2 .51 %;对初级生产力的摄食压力夏季为 1 1 5.2 3 %~1 93 .52 %、冬季为 3 7.47%~ 1 1 1 .3 1 %.  相似文献   

9.
2005年7月在台湾海峡南部4个站位应用“稀释法”结合高效液相色谱(HPLC)色素分析技术研究了不同色素类群浮游植物的生长率及微型浮游动物对其的摄食死亡率.结果表明,不同色素类群浮游植物的生长率(k)和摄食死亡率(g)分别为0.52~ 1.34 d-1和0.25 ~ 1.10 d-1,微型浮游动物对不同色素类群浮游植物的现存量和初级生产力的摄食压力分别为22%~ 66%和40%~ 151%.通过比较不同类群浮游植物的g/k值,发现颗粒较大的浮游植物(硅藻和甲藻)的净生长率要大于那些微型藻类(蓝细菌、隐藻和定鞭金藻等)的净生长率,说明本次研究中微型藻类更易受到微型浮游动物的摄食控制.  相似文献   

10.
台湾海峡小型浮游动物的摄食对夏季藻华演替的影响   总被引:3,自引:2,他引:3  
于2004年8月1~6日对台湾海峡南部近岸的藻华过程进行了定点连续跟踪观测,用稀释法研究了浮游植物的生长率和小型浮游动物对浮游植物的摄食死亡率,同时运用高效液相色谱(HPLC)技术,分析了浮游植物不同光合色素类群的生长率和摄食死亡率.结果表明,观测期间处于藻华的消退期.8月1日时,浮游植物生物量(叶绿素a)和丰度分别为2.04μg/dm3和2.99×105个/dm3,主要优势种为尖刺伪菱形藻(Pseudo-nitzschia pungens)、冰河拟星杆藻(Asterionellopsis glacialis)和中肋骨条藻(Skeletonema costatum),8月6日时,浮游植物生物量和丰度分别减为0.37μg/dm3和1.54×104个/dm3;而蓝藻和甲藻的丰度和比例则呈现出逐渐增加的趋势,所占的比重分别从1日的0.04%和0.85%增加到6日的9.59%和41.97%.小型浮游动物主要由无壳纤毛虫、砂壳纤毛虫、红色中缢虫(Mesodinium rubrum)和异养甲藻等类群组成,总丰度于8月2日达到最大值,为3640个/dm3,之后逐渐减少,6日时,仅为436个/dm3.观测期间,小型浮游动物在群落组成上虽一直以无壳纤毛虫和异养甲藻为主,但在具体的类群结构上却表现出了一定的差异,30μm以下的无壳纤毛虫和异养甲藻总体呈下降的趋势,而红色中缢虫、砂壳纤毛虫和大于50μm的无壳纤毛虫总体呈增加的趋势.观测期间,浮游植物的生长率为0.40~0.91d-1,小型浮游动物的摄食率为0.26~1.34d-1,摄食率和生长率总体呈逐渐下降的趋势.结果还表明,小型浮游动物的摄食率与叶绿素a具有很好的相关性(R2=0.89),对各光合色素类群的现存量和初级生产力均具有较高的摄食压力(分别为37.97%~82.24%和70.71%~281.33%),是藻华消亡的重要原因之一;此外,小型浮游动物对甲藻和蓝藻的避食行为,可能是观测期间由“硅藻”水华向“硅藻-甲藻”水华转变的重要原因之一.  相似文献   

11.
Phytoplankton group-specific growth and microzooplankton grazing were determined seasonally using the dilution technique with high-performance liquid chromatography (HPLC) in the Xiamen Bay, a subtropical bay in southeast China, between May 2003 and February 2004. The results showed that growth rates of phytoplankton ranged from 0.71 to 2.2 d^-1 with the highest value occurred in the inner bay in May. Mierozooplankton grazing rates ranged from 0.5 to 3.1 d^-1 with the highest value occurred in the inner bay in August. Microzooplankton grazing impact ranged from 39% to 95% on total phytoplankton Chl a biomass, and 65% to 181% on primary production. The growth and grazing rates of each phytoplankton group varied, the highest growth rate (up to 3.3 d^-1 ) was recorded for diatoms in August, while the maximum grazing rate ( up to 2.1 d ^-1 ) was recorded for chlorophytes in February in the inner bay. Among main phytoplankton groups, grazing pressure of microzooplankton ranged from 10% to 83% on Chl a biomass, and from 14% to 151% on primary production. The highest grazing pressure on biomass was observed for cryptophytes (83%) in August, while the maximum grazing pressure on primary production was observed for eyanobacteria (up to 151% ) in December in the inner bay. Net growth rates of larger phytoplanktons (diatoms and dinoflagellates) were higher than those of smaller groups ( prasinophytes, chlorophytes and cyanobacteria). Relative preference index showed that microzooplankton grazed preferentially on prasinophytes and avoided to harvest diatoms in cold seasons (December and February).  相似文献   

12.
为了解春夏季黄海和东海微型浮游动物类群及其摄食生态,于2011年春季和夏季在黄海、东海,通过稀释法测定浮游植物生长率及微型浮游动物对浮游植物的摄食率,同时应用显微分析技术研究了微型浮游动物丰度及其类群组成.结果表明:(1)春季,黄海、东海微型浮游动物丰度为1800~21833个/dm3,夏季的为67~6175个/dm3;春季,其微型浮游动物生物量为8.71-60.58ug/dm3,夏季的则为0.44~30.25ug/dm3(其生物量以c含量计).(2)春季、夏季黄海和东海浮游植物的生长率及其标准偏差分别为0.78±0.35、1.62±0.83d-1,而春季的显著低于夏季(P〈0.05).春季、夏季其微型浮游动物的摄食率及其标准偏差分别为0.98±0.32、0.92±0.57d-1,无显著性差异(p〉0.05).春季,微型浮游动物摄食浮游植物现有生物量的61%±13%,占初级生产量的131%±58%;夏季,微型浮游动物摄食浮游植物现有生物量的54%±22%,占初级生产量的70%±44%.春、夏季,黄海和东海微型浮游动物对浮游植物初级生产量的摄食比例较高.  相似文献   

13.
2000年秋季(10月21日-11月7日)和2001年春季(4月30日-5月15日)用稀释培养法在黄海和东海测定了微型浮游动物对浮游植物的摄食,结果表明:(1)秋季表层浮游植物叶绿素α(Chl α)的内禀生长率为0.40~0.59 d<'-1>,微型浮游动物对Chl α的摄食率为0.21~0.63 d<'-1>,对Ch...  相似文献   

14.
曾祥波  黄邦钦 《海洋学报》2008,30(6):140-146
为了研究小型浮游动物对近岸浮游植物藻华的摄食调控作用,于2005年7月,应用"稀释法"并结合高效液相色谱(HPLC)光合色素分析技术,研究了台湾海峡船基围隔实验条件下浮游植物生长率及小型浮游动物摄食率的日变动。结果表明:由于营养盐添加的影响,迅速形成了以尖刺伪菱形藻(Pseudo-nitzschia pungens)为优势种的藻华,生物量(叶绿素a)从实验初始7月6日的1.45μg/dm3迅速增加到7月8日的29.80μg/dm3,随后消退。镜检和光合色素分析的结果显示,实验期间一直以此硅藻占绝对优势。浮游植物的生长率在藻华峰值(7月8日)前保持了较高的生长速率(>1.0/d)且大于小型浮游动物的摄食率;小型浮游动物的摄食率也逐渐增加,7月7日时达到0.86/d,显示有57%以上的浮游植物现存量被摄食。7月8日后,水华迅速消退,摄食率除13日外,均大于浮游植物的生长率。小型浮游动物主要由急游虫(Strombidium spp.)、侠盗虫(Strobilidium spp.)等无壳纤毛虫、异养甲藻-螺旋环沟藻(Gyrodinium spirale)及砂壳纤毛虫等组成,其对浮游植物的生长迅速作出了反应,各类群的丰度在水华峰值后的7月9日均几达最大值,水华后期(11日)大型的无壳纤毛虫达最大值。小型浮游动物的这种组成及变动特点是其保持较高摄食率及一定程度上控制和促进藻华消退的原因之一。  相似文献   

15.
During late winter and spring of 2002 and 2003, 24 two- to three-day cruises were conducted to Dabob Bay, Washington State, USA, to examine the grazing, egg production, and hatching success rates of adult female Calanus pacificus and Pseudocalanus newmani. Here, we discuss the results of our grazing experiments for P. newmani. Each week, we conducted traditional microzooplankton dilution experiments and “copepod dilution” experiments, each from two different layers. Grazing was measured by changes in chlorophyll concentration and direct cell counts. Clearance rates on individual prey species, as calculated by cell counts, showed that Pseudocalanus are highly selective in their feeding, and may have much higher grazing rates on individual taxa than calculated from bulk chlorophyll disappearance. The grazing rates of the copepods, however, are typically an order of magnitude lower than the grazing rates of the microzooplankton community, or the growth rates of the phytoplankton. P. newmani ingested diatoms, but, at certain times fed preferentially on microzooplankton, such as ciliates, tintinnids, and larger dinoflagellates. Removal of the microzooplankton may have released the other phytoplankton species from grazing pressure, allowing those species’ abundance to increase, which was measured as an apparent “negative” grazing on those phytoplankton species. The net result of grazing on some phytoplankton species, while simultaneously releasing others from grazing pressure resulted in bulk chlorophyll-derived estimates of grazing which were essentially zero or slightly negative; thus bulk chlorophyll disappearance is a poor indicator of copepod grazing. Whether copepods can significantly release phytoplankton from the grazing pressure by microzooplankton in situ, thus causing a trophic cascade, remains to be verified, but is suggested by our study.  相似文献   

16.
Using the seawater dilution technique, we measured phytoplankton growth and microzooplankton grazing rates within and outside of the 1999 Bering Sea coccolithophorid bloom. We found that reduced microzooplankton grazing mortality is a key component in the formation and temporal persistence of the Emiliania huxleyi bloom that continues to proliferate in the southeast Bering Sea. Total chlorophyll a (Chl a) at the study sites ranged from 0.40 to 4.45 μg C l−1. Highest phytoplankton biomass was found within the bloom, which was a mixed assemblage of diatoms and E. huxleyi. Here, 75% of the Chl a came from cells >10 μm and was attributed primarily to the high abundance of the diatom Nitzschia spp. Nutrient-enhanced total phytoplankton growth rates averaged 0.53 d−1 across all experimental stations. Average growth rates for >10 μm and <10 μm cells were nearly equal, while microzooplankton grazing varied among stations and size fractions. Grazing on phytoplankton cells >10 μm ranged from 0.19 to 1.14 d−1. Grazing on cells <10 μm ranged from 0.02 to 1.07 d−1, and was significantly higher at non-bloom (avg. 0.71 d−1) than at bloom (avg. 0.14 d−1) stations. Averaged across all stations, grazing by microzooplankton accounted for 110% and 81% of phytoplankton growth for >10 and <10 μm cells, respectively. These findings contradict the paradigm that microzooplankton are constrained to diets of nanophytoplankton and strongly suggests that their grazing capability extends beyond boundaries assumed by size-based models. Dinoflagellates and oligotrich ciliates dominated the microzooplankton community. Estimates of abundance and biomass for microzooplankton >10 μm were higher than previously reported for the region, ranging from 22,000 to 227,430 cells l−1 and 18 to 164 μg C l−1. Highest abundance and biomass occurred in the bloom and corresponded with increased abundance of the large ciliate Laboea, and the heterotrophic dinoflagellates Protoperidinium and Gyrodinium spp. Despite low grazing rates on phytoplankton <10 μm within the bloom, the abundance and biomass of small microzooplankton (<20 μm) capable of grazing E. huxleyi was relatively high at bloom stations. This body of evidence, coupled with observed high grazing rates on large phytoplankton cells, suggests the phytoplankton community composition was strongly regulated by herbivorous activity of microzooplankton. Because grazing behavior deviated from size-based model predictions and was not proportional to microzooplankton biomass, alternate mechanisms that dictate levels of grazing activity were in effect in the southeastern Bering Sea. We hypothesize that these mechanisms included morphological or chemical signaling between phytoplankton and micrograzers, which led to selective grazing pressure.  相似文献   

17.
To investigate the seasonal variation and community structure of nano- and microzooplankton in Gyeonggi Bay of the Yellow Sea, the abundance and carbon biomass of nano- and microzooplankton were evaluated at 10-day intervals from January 1997 to December 1999. Four major groups of nano- and microzooplankton communities were classified: heterotrophic ciliates, heterotrophic dinoflagellates (HDF), heterotrophic nanoflagellates (HNF), and copepod nauplii. The total carbon biomass of nano- and microzooplankton ranged from 10.2 to 168.8 μg C L−1 and was highest during or after phytoplankton blooms. Nano- and microzooplankton communities were composed of heterotrophic ciliates (7.4–81.4%; average 41.7% of total biomass), HDF (0.1–70.3%; average 26.1% of total biomass), copepod nauplii (1.6–70.6%; average 20.7% of total biomass), and HNF (0.8–59.5%; average 11.5% of total biomass). The relative contribution of individual components in the nano- and microzooplankton communities appeared to differ by seasons. Ciliates accounted for the most major component of nano- and microzooplankton communities, except during summer and phytoplankton blooming seasons, whereas HDF were more dominant during the phytoplankton blooming seasons. The abundance and biomass of nano- and microzooplankton generally followed the seasonal dynamics of phytoplankton. The size and community distribution of nano- and microzooplankton was positively correlated with size-fractionated phytoplankton. The carbon requirement of microzooplankton ranged from 60 to 83% of daily primary production, and was relatively high when phytoplankton biomass was high. Therefore, our result suggests that the seasonal variation in the community and size composition of nano- and microzooplankton appears to be primarily governed by phytoplankton size and concentration as a food source, and their abundance may greatly affect trophic dynamics by controlling the seasonal abundance of phytoplankton.  相似文献   

18.
Phytoplankton growth rates and mortality rates were experimentally examined at 21 stations during the 2017 spring intermonsoon(April to early May) in the northern and central South China Sea(SCS) using the dilution technique, with emphasis on a comparison between the northern and central SCS areas which had different environmental factors. There had been higher temperature but lower nutrients and chlorophyll a concentrations in the central SCS than those in the northern SCS. The mean rates of phytoplankton growth(μ_0) and microzooplankton grazing(m) were(0.88±0.33) d~(–1) and(0.55±0.22) d~(–1) in the central SCS, and both higher than those in the northern SCS with the values of μ_0((0.81±0.16) d~(–1)) and m((0.30±0.09) d~(–1)), respectively.Phytoplankton growth and microzooplankton grazing rates were significantly coupled in both areas. The microzooplankton grazing impact(m/μ_0) on phytoplankton was also higher in the central SCS(0.63±0.12) than that in the northern SCS(0.37±0.06). The microzooplankton abundance was significantly correlated with temperature in the surface. Temperature might more effectively promote the microzooplankton grazing rate than phytoplankton growth rate, which might contribute to higher m and m/μ_0 in the central SCS. Compared with temperature, nutrients mainly affected the growth rate of phytoplankton. In the nutrient enrichment treatment,the phytoplankton growth rate(μn) was higher than μ_0 in the central SCS, suggesting phytoplankton growth in the central SCS was nutrient limited. The ratio of μ_0/μn was significantly correlated with nutrients concentrations in the both areas, indicating the limitation of nutrients was related to the concentrations of background nutrients in the study stations.  相似文献   

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