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1.
The source and significance of two nutrients, nitrogen and phosphorous, were investigated by a modified dilution method performed on seawater samples from the Jiaozhou Bay, in autumn 2004. This modified dilution method accounted for the phytoplankton growth rate, microzooplankton grazing mortality rate, the internal and external nutrient pools, as well as nutrient supplied through remineralization by microzooplankton. The results indicated that the phytoplankton net growth rate increased in turn from inside the bay, to outside the bay, to in the Xiaogang Harbor. The phytoplankton maximum growth rates and microzooplankton grazing mortality rates were 1.14 and 0.92 d-1 outside the bay, 0.42 and 0.32 d-1 inside the bay and 0.98 and 0.62 d-1 in the harbor respectively. Outside the bay, the remineralized nitrogen (Kr=24.49) had heavy influence on the growth of the phytoplankton. Inside the bay, the remineralized phosphorus(Kr=3.49) strongly affected the phytoplankton growth. In the harbor, the remineralized phosphorus (Kr=3.73) was in larger demand by phytoplankton growth. The results demonstrated that the different nutrients pools supplied for phytoplankton growth were greatly in accordance with the phytoplankton community structure, microzooplankton grazing mortality rates and environmental conditions. It is revealed that nutrient remineralization is much more important for the phytoplankton growth in the Jiaozhou Bay than previously believed. 相似文献
2.
Phytoplankton growth and microzooplankton grazing were studied during the 2007 spring bloom in Central Yellow Sea. The surveyed stations were divided to pre-bloom phase (Chl a concentration less than 2 μg L−1), and bloom phase (Chl a concentration greater than 2 μg L−1). Shipboard dilution incubation experiments were carried out at 19 stations to determine the phytoplankton specific growth rates and the specific grazing rates of microzooplankton on phytoplankton. Diatoms dominated in the phytoplankton community in surface waters at most stations. For microzooplankton, Myrionecta rubra and tintinnids were dominant, and heterotrophic dinoflagellate was also important in the community. Phytoplankton-specific growth rates, with an average of 0.60±0.19 d−1, were higher at pre-bloom stations (average 0.62±0.17 d−1), and lower at the bloom stations (average 0.59±0.21 d−1), but the difference of growth rates between bloom and pre-bloom stations was not statistically significant (t test, p=0.77). The phytoplankton mortality rate by microzooplankton grazing averaged 0.41±0.23 d−1 at pre-bloom stations, and 0.58±0.31 d−1 during the blooms. In contrast to the growth rates, the statistic difference of grazing rates between bloom and pre-bloom stations was significant (after removal of outliers, t test, p=0.04), indicating the importance of the top-down control in the phytoplankton bloom processes. Average potential grazing efficiency on primary productivity was 66% at pre-bloom stations and 98% at bloom stations, respectively. Based on our results, the biomass maximum phase (bloom phase) was not the maximum growth rate phase. Both phytoplankton specific growth rate and net growth rate were higher in the pre-bloom phase than during the bloom phase. Microzooplankton grazing mortality rate was positively correlated with phytoplankton growth rate during both phases, but growth and grazing were highly coupled during the booming phase. There was no correlation between phytoplankton growth rate and cell size during the blooms, but they were positive correlated during the pre-bloom phase. Our results indicate that microzooplankton grazing is an important process controlling the growth of phytoplankton in spring bloom period in the Central Yellow Sea, particularly in the “blooming” phase. 相似文献
3.
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
4.
Dilution experiments were conducted to investigate microzooplankton grazing impact on phytoplankton of different taxonomic groups and size fractions (< 5, 5–20, 20–200 μm) during spring and summer bloom periods at two different sites (inner Tolo Harbour and Tolo Channel) in the Tolo Harbour area, the northeastern coastal area of Hong Kong. Experiments combined with HPLC pigment analysis in three phytoplankton size fractions measured pigment and size specific phytoplankton growth rates and microzooplankton grazing rates. Pigment-specific phytoplankton growth rates ranged between 0.08 and 3.53 d− 1, while specific grazing rates of microzooplankton ranged between 0.07 and 2.82 d− 1. Highest specific rates of phytoplankton growth and microzooplankton grazing were both measured in fucoxanthin in 5–20 μm size fraction in inner Tolo Harbour in summer, which coincided with the occurrence of diatom bloom. Results showed significant correlations between phytoplankton growth and microzooplankton grazing rates. Microzooplankton placed high grazing pressure on phytoplankton community. High microzooplankton grazing impact on alloxanthin (2.63–5.13) suggested strong selection toward cryptophytes. Our results provided no evidence for size selective grazing on phytoplankton by microzooplankton. 相似文献
5.
A sequence of nine dilution experiments was conducted according to Landry and Hassett [Landry, M.R., Hassett, R.P., 1982. Estimating the grazing impact of marine microzooplankton. Mar. Biol. 67, 283–288] in the northern Wadden Sea from March until October 2004 to investigate the seasonality of microzooplankton grazing. From March until April, no grazing was observed. Microzooplankton grazing started in May (0.66 d− 1) and increased until August (1.22 d− 1). In October microzooplankton grazing was low again (0.17 d− 1). Phytoplankton growth rates varied between 0 and 1.1 d− 1. Since the reliability of dilution experiments is still frequently discussed in literature, we tested if our data obtained by dilution experiments reflected short-term in situ phytoplankton dynamics of the study site. We scaled experimental growth rates to water column irradiance, calculated short-term chlorophyll-a dynamics and compared the results to in situ measured chlorophyll-a concentrations. Calculated chlorophyll-a concentrations correlated significantly with in situ measured chlorophyll-a concentrations but slightly overestimated the in situ measured chlorophyll-a. This overestimation was in the range of phytoplankton assimilation reported for the Wadden Sea benthos. We will show that microzooplankton grazing had a large impact during the Phaeocystis bloom and during summer suggesting that a large proportion of phytoplankton biomass remained the pelagic food web. Microzooplankton grazing did not impact the diatom spring bloom and its demise. 相似文献
6.
《Journal of Sea Research》2009,61(4):246-254
The aim of this study was to investigate controls on the phytoplankton community composition and biogeochemistry of the estuarine plume zone of the River Thames, U.K. using an instrumented moored buoy for in situ measurements and preserved sample collection, and laboratory-based measurements from samples collected at the same site. Instrumentation on the moored buoy enabled high frequency measurements of a suite of environmental variables including in situ chlorophyll, water-column integrated irradiance, macronutrients throughout an annual cycle for 2001 e.g. nitrate and silicate, and phytoplankton biomass and species composition. The Thames plume region acts as a conduit for fluvial nutrients into the wider southern North Sea with typical winter concentrations of 45 μM nitrate, 17 μM silicate and 2 μM phosphate measured. The spring bloom resulted from water-column integrated irradiance increasing above 60 W h m− 2 d− 1 and was initially dominated by a diatom bloom mainly composed of Nitzschia sp. and Odontella sinesis. The spring bloom then switched after ∼ 30 days to become dominated by the flagellate Phaeocystis reaching a maximum chlorophyll concentration of 37.8 μg L− 1. During the spring bloom there were high numbers of the heterotrophic dinoflagellates Gyrodinium spirale and Katodinium glaucum that potentially grazed the phytoplankton bloom. This diatom–flagellate switch was predicted to be due to a combination of further increasing water-column integrated irradiance > 100 W h m− 2 d− 1 and/or silicate reaching potentially limiting concentrations (< 1 μM). Post spring bloom, diatom dominance of the lower continuous summer phytoplankton biomass occurred despite the low silicate concentrations (Av. 0.7 μM from June–August). Summer diatom dominance, generally due to Guinardia delicatula, was expected to be as a result of microzooplankton grazing, dominated by the heterotrophic dinoflagellate Noctiluca scintillans, controlling 0.7–5.0 μm ‘flagellate’ fraction of the phytoplankton community with grazing rates up to 178% of ‘flagellate’ growth rate. The Thames plume region was therefore shown to be an active region of nutrient and phytoplankton processing and transport to the southern North Sea. The use of a combination of moorings and ship-based sampling was essential in understanding the factors influencing nutrient transport, phytoplankton biomass and species composition in this shelf sea plume region. 相似文献
7.
8.
M. Brady Olson Suzanne L. Strom 《Deep Sea Research Part II: Topical Studies in Oceanography》2002,49(26)
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
9.
Hongbin Liu Koji Suzuki Jun Nishioka Rumi Sohrin Takeshi Nakatsuka 《Deep Sea Research Part I: Oceanographic Research Papers》2009,56(4):561-570
The Sea of Okhotsk is one of the most productive marine basins in the world ocean and plays an important role in transport of organic carbon and iron to the western subarctic Pacific. We report the first measurements of phytoplankton growth and microzooplankton grazing rates in the Sea of Okhotsk, in late summer of 2006. The study area can be divided into two areas: nutrient-sufficient waters on the continental shelf along the east coast of Sakhalin Island and in the vicinity of Bussol Strait, and surface nutrient-depleted waters beyond the shelf break and in the vicinity of Sakhalin Bay. Phytoplankton growth rate in the studied area was strongly affected by nutrient availability, with high phytoplankton growth rate (0.55±0.14 d?1) in the nutrient-replete region and severely depressed growth (0.03±0.05 d?1) in the nutrient-depleted region. On the other hand, microzooplankton grazing rates in both the nutrient-replete and nutrient-depleted regions were approximately the same (0.26±0.20 d?1 vs. 0.27±0.24 d?1). Consequently, microzooplankton grazing consumed <50% of the phytoplankton growth in nutrient-rich waters but >3 times the phytoplankton growth in nutrient-depleted waters. Phytoplankton physiological condition as measured by the maximum photochemical quantum efficiency (Fv/Fm) of algal photosystem II (PS II) showed a general trend in agreement with the in situ growth rate of phytoplankton. In contrast to the phytoplankton community, picophytoplankton, especially the cyanobacteria Synechococcus, showed no nutrient effect on their growth, and the growth and mortality rates were well balanced, suggesting that they have a low nutrient requirement and their biomass was controlled principally by microzooplankton grazing. 相似文献
10.
《Deep Sea Research Part I: Oceanographic Research Papers》2002,49(2):363-375
Phytoplankton growth and microzooplankton grazing rates were measured by the dilution technique in the subarctic North Pacific Ocean along a west–east transect during summer 1999. Average phytoplankton growth rates without added nutrients (μ0) were 0.33, 0.41, 0.20 and 0.49 d−1 for the four regions sampled: the Western Gyre, the Bering Sea, the Gulf of Alaska gyre and stations along the Aleutian Trench. Average grazing mortality rates (m) were 0.34, 0.27, 0.20 and 0.49 d−1. Limitation of phytoplankton growth by macronutrients, such as NO3 and SiO2, was identified only at a few stations, with overall μ0/μn (μn is nutrient-enhanced growth rate) averaging 0.9. Phytoplankton growth and microzooplankton grazing were approximately balanced, as indicated by high m/μ0 ratio, except in the Bering Sea, where the m/μ0 ratio was 0.65, indicating the relative importance of the diatom-macrozooplankton grazing food chain and possible higher export flux to the deep layer. Flow cytometric analysis revealed that the growth rates of picoplankton (Synechococcus and picoeukaryotes) were usually much lower than the total phytoplankton community growth rates estimated from chlorophyll a, except for stations in the Gulf of Alaska Gyre, where the growth rates for different populations were about the same. Lower than community-average growth rate for picoplankton indicates larger phytoplankters, presumably diatoms, were growing at a much faster rate. Suppressed phytoplankton growth in the Gulf of Alaska was probably a result of iron limitation. 相似文献
11.
《Journal of Sea Research》2000,43(3-4):345-356
During spring blooms 1998 and 1999, three complementary methods were used to evaluate the in situ feeding activities of the dominant copepod species of the Belgian coastal zone: gut pigment content analysis using HPLC, the 14C tracer method, and cell count experiments. The results obtained by all three methods consistently showed that Phaeocystis globosa is not an adequate food source for the spring copepods in the Belgian coastal zone. Our results demonstrated that, among the potential prey, copepods strongly selected diatoms and microzooplankton, and that these types of prey accounted for the major part of the ingested carbon. However, diatoms and microzooplankton ingestion did not always seem sufficient in terms of carbon to avoid food limitation. Comparison of clearance rates exerted on different potential prey types during the P. globosa peak with those before and after the P. globosa peak showed that the copepods' feeding pressure on diatoms was reduced during the P. globosa peak while that on microzooplankton was not. The low grazing pressure on P. globosa, together with the preferential grazing on diatoms, which reduces the competition for nutrients, and the predation on microzooplankton organisms, which reduces the microzooplankton grazing pressure on P. globosa cells, are likely to favour the P. globosa bloom in the Southern Bight of the North Sea. 相似文献
12.
2011年春夏季黄海和东海微型浮游动物类群组成及其摄食的研究 总被引：1，自引：0，他引：1
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.
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
14.
《Deep Sea Research Part II: Topical Studies in Oceanography》2009,56(17):1264-1273
Microzooplankton grazing impact on phytoplankton was assessed using the Landry–Hassett dilution technique in the Western Arctic Ocean during spring and summer 2002 and 2004. Forty experiments were completed in a region encompassing productive shelf regions of the Chukchi Sea, mesotrophic slope regions of the Beaufort Sea off the North Slope of Alaska, and oligotrophic deep-water sites in the Canada Basin. A variety of conditions were encountered, from heavy sea-ice cover during both spring cruises, moderate sea-ice cover during summer of 2002, and light to no sea ice during summer of 2004, with a concomitant range of trophic conditions, from low chlorophyll-a (Chl-a; <0.5 μg L−1) during heavy ice cover in spring and in the open basin, to late spring and summer shelf and slope open-water diatom blooms with Chl-a >5 μg L−1. The microzooplankton community was dominated by large naked ciliates and heterotrophic gymnodinoid dinoflagellates. Significant, but low, rates of microzooplankton herbivory were found in half of the experiments. The maximum grazing rate was 0.16 d−1 and average grazing rate, including experiments with no significant grazing, was 0.04±0.06 d−1. Phytoplankton intrinsic growth rates varied from the highest values of about 0.4 d−1 to the lowest values of zero to slightly negative growth, on average 0.16±0.15 d−1. Light limitation in spring and post-bloom senescence during summer were likely explanations of observed low phytoplankton growth rates. Microzooplankton grazing consumed 0–120% (average 22±26%) of phytoplankton daily growth. Grazing and growth rates found in this study were low compared to rates reported in another Arctic system, the Barents Sea, and in major geographic regions of the world ocean. 相似文献
15.
The new diatom species Mediopyxis helysia was described to science from clones found in 2003 in the North Sea, northern Wadden Sea, and the Gulf of Maine. Seven years after its first occurrence, we observed Mediopyxis to contribute up to almost 50% of the biovolume of the diatoms during a diatom spring bloom in the western Wadden Sea. Grazing experiments based on the dilution technique could not detect any microzooplankton grazing impact on the bloom community. Mediopyxis is now also well established in the western Wadden Sea and does have the potential to become a dominant species. The reasons for its success remain largely unresolved but avoidance of being grazed might be one factor. Future research on this new species is needed to understand the success and forecast the ecological footprint of this large diatom species arriving in the western European Seas. 相似文献
16.
Julian P. McCreary Jr Kevin E. Kohler Raleigh R. Hood Donald B. Olson 《Progress in Oceanography》1996,37(3-4)
A coupled, physical-biological model is used to study the processes that determine the annual cycle of biological activity in the Arabian Sea. The physical model is a
system with a surface mixed layer imbedded in the upper layer, and fluid is allowed to move between layers via entrainment, detrainment and mixing processes. The biological model consists of a set of advective-diffusive equations in each layer that determine the nitrogen concentrations in four compartments: nutrients, phytoplankton, zooplankton and detritus. Coupling is provided by the horizontal-velocity, layer-thickness, entrainment and detrainment fields from the physical solution. Surface forcing fields (such as wind stress and photosynthetically active radiation) are derived from monthly climatological data, and the source of nitrogen for the system is upward diffusion of nutrients from the deep ocean into the lower layer. Our main-run solution compares favorably with observed physical and biological fields; in particular, it is able to simulate all the prominent phytoplankton blooms visible in the CZCS data. Three bloom types develop in response to the physical processes of upwelling, detrainment and entrainment. Upwelling blooms are strong, long-lasting events that continue as long as the upwelling persists. They occur during the Southwest Monsoon off Somalia, Oman and India as a result of coastal alongshore winds, and at the mouth of the Gulf of Aden through Ekman pumping. Detrainment blooms are intense, short-lived events that develop when the mixed layer thins abruptly, thereby quickly increasing the depth-averaged light intensity available for phytoplankton growth. They occur during the fall in the central Arabian Sea, and during the spring throughout most of the basin. In contrast to the other bloom types, entrainment blooms are weak because entrainment steadily thickens the mixed layer, which in turn decreases the depth-averaged light intensity. There is an entrainment bloom in the central Arabian Sea during June in the solution, but it is not apparent in the CZCS data. Bloom dynamics are isolated in a suite of diagnostic calculations and test solutions. Some results from these analyses are the following. Entrainment is the primary nutrient source for the offshore bloom in the central Arabian Sea, but advection and recycling also contribute. The ultimate cause for the decay of the solution's spring (and fall) blooms is nutrient deprivation, but their rapid initial decay results from grazing and self shading. Zooplankton grazing is always an essential process, limiting phytoplankton concentrations during both bloom and oligotrophic periods. Detrital remineralization is also important: in a test solution without remineralization, nutrient levels drop markedly in every layer of the model and all blooms are severely weakened. Senescence, however, has little effect: in a test solution without senescence, its lack is almost completely compensated for by increased grazing. Finally, the model's detrainment blooms are too brief and intense in comparison to the CZCS data; this difference cannot be removed by altering biological parameters, which suggests that phytoplankton growth in the model is more sensitive to mixed-layer thickness than it is in the real ocean. 相似文献
17.
The balance between microzooplankton grazing and phytoplankton growth in a highly productive estuarine fjord 总被引：1，自引：4，他引：1
Andrew W. Leising Rita Horner James J. Pierson James Postel Claudia Halsband-Lenk 《Progress in Oceanography》2005,67(3-4):366
During 24, three-day cruises to Dabob Bay, Washington State, USA, from February 4 to April 26, 2002, and February 4 to May 1 2003, we examined the relative growth and grazing rates of phytoplankton and microzooplankton using dilution experiments. Experiments were conducted over two time intervals: 8–10 h during the nighttime only, or 24 h from noon to noon. We used water from two depths during each cruise: from the surface mixed layer, and from a deep layer below the seasonal thermocline. During 2002, there was one mid-sized bloom consisting mainly of Thalassiosira spp. in early February, and a larger bloom in April comprised of two Chaetoceros spp. and Phaeocystis sp. During 2003, there were also two blooms, one in early February, which was again dominated by Thalassiosira spp., and a second larger bloom in mid-April, comprised mainly of Thalassiosira spp. and Chaetoceros spp. During all four of these blooms, and for both water source depths, specific grazing rates of microzooplankton were most often as high or higher than the calculated phytoplankton specific growth rates. The major microzooplankton categories that could have accounted for this were (1) a large Gyrodinium spp., (2) a group of fusiform-shaped mid-sized Protoperidinium species, and (3) three loosely defined taxonomic groups consisting of naked ciliates, tintinnids, and unidentified heterotrophic dinoflagellates. Based on our measurements, it appears that the microzooplankton community grazing pressure can often exert significant control on phytoplankton biomass, even during the extremely productive spring bloom periods and under several different diatom-dominated bloom types. These results suggest that even in highly productive estuarine ecosystems, which are often nurseries to economically important fisheries species, microzooplankton play a critical role and may significantly alter the availability and efficiency of transfer of energy to higher trophic levels. 相似文献
18.
Suhaimi Suratman Keith Weston Naomi Greenwood David B. Sivyer David J. Pearce Tim Jickells 《Estuarine, Coastal and Shelf Science》2010
The aim of this study was to investigate the cycling of dissolved inorganic and organic nutrients using moored instrumented buoys (SmartBuoys) during the spring bloom in the North Sea. The instrumentation on the buoys enabled high frequency measurements of water-column integrated irradiance and in situ chlorophyll to be made, and also preserved water sample collection which were used for dissolved inorganic and organic nutrient analyses. The SmartBuoys were located in the year-round well-mixed plume zone associated with the River Thames and in the summer stratified central North Sea. These site locations allowed comparison of nutrient concentrations and cycling, and spring bloom development at two contrasting sites. The spring bloom was expected to be initiated at both stations due to increasing insolation and decreasing suspended load leading to higher water-column integrated irradiance. Due to differences in suspended load between the sites, the spring bloom started ∼2 months earlier in the central North Sea. The spring bloom in the Thames plume also resulted in higher maximum phytoplankton biomass due to the higher pre-bloom nutrient concentrations associated with riverine input. The use of SmartBuoys is also shown to allow the cycling of dissolved organic nutrients to be examined over the critical, and often undersampled, spring bloom period. Dissolved Organic Nitrogen (DON) clearly increased during the spring bloom in the central North Sea compared to winter concentrations. DON also increased in the Thames plume although showing greater winter variability related to higher riverine and sedimentary dissolved organic matter input at this shallow (∼18 m) coastal site. DON increase during the spring bloom was therefore related to primary production at both sites probably due to active release by phytoplankton. At both stations DON decreased to pre-bloom concentrations as the bloom declined suggesting the released DON was bioavailable and removed due to heterotrophic uptake and production. The preserved nutrient samples from the central North Sea site were also suitable for Dissolved Organic Phosphorus (DOP) analysis due to their low suspended load with similar trends and cycling to DON, albeit at lower concentrations. This suggested similar processes controlling both DON and DOP. The variable timing of short term events such as the spring bloom makes sampling away from coastal regions difficult without the use of autonomous technology. This study demonstrates for the first time the applicability of using preserved samples from automated buoys for the measurement of dissolved organic nutrients. 相似文献
19.
Experiments on nutrient and iron amendments were performed with phytoplankton on the eastern shelf of the Bering Sea in June 2000 and August 2001. The nutrient amendments (NO3, NH4, SiO4, NO3 + SiO4, NH4 + SiO4, and Fe + NO3) increasing their initial concentrations by ～20 μM were put into test bottles 10 l in volume each. With iron addition (Fe or Fe + NO3), its concentration increased by 5 nM. The experiments performed showed that the main nutrient that limited the phytoplankton development was nitrogen. Regardless of the composition of the dominant algae in the background community, the amendments caused massive development of diatoms. The intense growth was characteristic for diatoms of both the spring and spring-summer assemblages. At high abundances of Phaeocystis pouchetii or of the coccolithophore Emiliania huxleyi in the natural water, nitrogen-containing amendments caused an intense growth of these species, along with the massive development of diatoms. In the case of the diatom prevalence in the initial sample, the intensities of the utilization of NO3 and NH4 in combination with SiO4 in the course of the experiment were 1.7 and 3 times as high as their intensities with no silicon amendments. Likewise, NO3 + SiO4 and NH4 + SiO4 mixed amendments caused an increase in the silicon assimilation by a factor of 4–5 as compared to pure silicon amendments. During one of the experimental series in which both diatoms and Phaeocystis pouchetii actively developed, virtually complete nitrogen utilization (90–99.8%) in 4–5 days was observed for both the NO3 and NH4. The addition of silicon and iron only caused no significant growth of the phytoplankton abundance. It was assumed that the destruction of the seasonal thermocline and the supply of nutrients into the surface layer as a result of strong wind forcing might cause a phytoplankton bloom in the summer time and result in the much pronounced qualitative and quantitative spatial heterogeneity of the phytoplankton characteristic of the eastern shelf of the Bering Sea. 相似文献
20.
稀释法(dilution technique)是研究微型浮游动物摄食和浮游植物生长的常用方法之一,负值浮游植物生长率是稀释实验中常见的现象。分析了造成负值生长率出现的因素,以及这些因素对实验结果的影响,并提出了防止不利影响产生的措施。负值生长率的出现不能简单地视为实验失败的标志,培养光照和温度条件、取样误差、无颗粒水污染、营养盐污染和限制等都可能造成负生长率的出现,且对实验结果的影响不同。同时,根据实验结果,演示浮游植物光适应、取样误差、无颗粒水污染和加富营养盐对稀释实验的影响。结果显示,光照条件可以改变细胞色素含量,且不同浮游植物类群对光照条件的响应不同,从而导致基于色素分析的稀释实验结果出现误差;取样混合不均,可造成取值偏低,导致浮游植物生长率估值偏低,甚至为负值,但可能不影响对摄食率的估算。另外,实验污染(无颗粒水和加富营养盐污染)往往会抑制浮游植物生长,甚至造成浮游植物死亡。因此,培养条件模拟和人为干扰控制是稀释实验成功的关键。 相似文献