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The distribution of physical and chemical parameters and theirimpact on the biomass and abundance of phytoplankton in theWestern Pacific Ocean were compared in two opposing situations:the El Niño Southern Oscillation (ENSO) event of 1987and the non-ENSO period of 1988. During El Niño conditions(September 1987), maximum cell abundance was recorded at 10°Sat the boundary between the South Equatorial Current (SEC) andthe South Equatorial Countercurrent (SECC). In September 1988,after the return of non-ENSO conditions, a well-establishedequatorial upwelling produced an increase in the surface layernutrient supply over 7° of latitude. This in turn causedan increase in phytoplankton populations in the upper layer,with chlorophyll concentrations >0.2 mg m–3 and cyanobacteriaand microalgae populations >8.0x106 l–1 and >1.2x106l–1 respectively. Integrated over 120 m, the cyanobacteriaand microalgae populations were respectively 4.7 and 3.2 timeslarger than the year before. On the other hand, transient nutrientinputs such as those observed at 10°S in September 1987caused a large increase in cyanobacteria populations (4.4 times),compared with those in neighbouring zones, and a somewhat smallerincrease in microalgae populations (1.3 times). Cyanobacteriapopulations were much larger than those of microalgae in the80–100 m upper layer, whereas the latter were more numerousat that depth and below the chorophyll maximum. Population variationsin cyanobacteria were accompanied by changes in form, size andfluorescence of the cells. The analysis of the 52 profiles ofdepth distribution of cyanobacteria and microalgae shows howthe community structure is related to the depth and gradientof the nitracline.  相似文献   
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 Phytoplankton biomass, community structure and productivity of the Great Astrolabe lagoon and surrounding ocean were studied using measurements of chlorophyll concentration and carbon uptake. The contribution of picophytoplankton to biomass, productivity and community structure was estimated by size fractionation, 14C-incubation and flow cytometry analysis. Picoplankton red fluorescence was demonstrated to be a proxy for chlorophyll <3 μm. Consequently, the percentage contribution to chl a<3 μm from each picoplankton group could be calculated using regression estimated values of ψ i (fg chl a per unit of red fluorescence). In the lagoon, average chlorophyll concentration was 0.8 mg m-3 with 45% of phytoplankton <3 μm. Primary production reached 1.3 g C m-2 day-1 with 53% due to phytoplankton <3 μm. Synechococcus was the most abundant group at all stations, followed by Prochlorococcus and picoeukaryotes. At all stations, Prochlorococcus represented less than 4% of the chl a <3 μm, Synechococcus between 85 and 95%, and Picoeukaryotes between 5 and 10%. In the upper 40 m of surrounding oceanic waters, phytoplankton biomass was dominated by the >3 μm size fraction. In deeper water, the <1 μm size fraction dominated. Prochlorococcus was the most abundant picoplankton group and their contributions to the chlorophyll a<3 μm were close to that of the picoeukaryotes (50% each). Accepted: 27 May 1999  相似文献   
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A cyclostat was designed for growing the oceanic oxyphotobacterium Prochlorococcus PCC 9511. Culture of this organism, known to bedifficult to grow, was mastered for a large volume. Prochlorococcusgrew well and axenic conditions were maintained for up to 15 days. Wedesigned an illumination system allowing a smooth bell-shaped irradiancecurve reaching almost 1000 mol quanta m-2 s-1 tobe obtained. Cell division was strongly synchronised under theseillumination conditions, which were close to those found at low latitude inthe upper layer of ocean. The described device is particularly well suited tomake experiments requiring up to 6 L per day of well synchronised,exponentially-growing Prochlorococcus culture.  相似文献   
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G protein-coupled receptors (GPCRs) are involved in most physiological processes, many of them being engaged in fully differentiated cells. These receptors couple to transducers of their own, primarily G proteins and β-arrestins, which launch intracellular signalling cascades. Some of these signalling events regulate the translational machinery to fine-tune general cell metabolism or to alter protein expression pattern. Though extensively documented for tyrosine kinase receptors, translational regulation by GPCRs is still poorly appreciated. The objective of this review paper is to address the following questions: i) is there a “GPCR signature” impacting on the translational machinery, and ultimately on the type of mRNA translated? ii) are the regulatory networks involved similar as those utilized by tyrosine kinase receptors? In particular, we will discuss the specific features of translational control mediated by GPCRs and highlight the intrinsic properties of GPCRs these mechanisms could rely on.  相似文献   
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Cuet  P.  Atkinson  M. J.  Blanchot  J.  Casareto  B. E.  Cordier  E.  Falter  J.  Frouin  P.  Fujimura  H.  Pierret  C.  Susuki  Y.  Tourrand  C. 《Coral reefs (Online)》2011,30(1):45-55

Productivity, nutrient input, nutrient uptake, and release rates were determined for a coral-dominated reef flat at La Réunion, France, to assess the influence of groundwater nitrogen on carbon and nutrient budgets. Water samples were collected offshore in the ocean, at the reef crest and back reef for nutrients, picoplankton, pH, and total alkalinity. Volume transport of ocean water across the reef flat was measured using both current meters and drogues. Groundwater advected onto the reef flat and mixed with incoming ocean water. Metabolic rates for the reef community were determined to be: gross primary production = 1,000 mmol C m−2 d−1, community respiration = 960 mmol C m−2 d−1, and community calcification = 210 mmol C m−2 d−1. Across the reef flat, silicate behaved conservatively, there was net uptake of phosphate (0.06 mmol P m−2 d−1) and net release of nitrate, ammonia, dissolved and particulate organic nitrogen (total 7.0 mmol N m−2 d−1). Groundwater nitrate contributed 37% of the increase in nitrate plus ammonia. The first-order mass transfer coefficient of phosphate was 3.3 m d−1, and for nitrate plus ammonia, 5.9 m d−1. Gross N and P uptake from estimates of mass transfer and uptake of particles were 0.37 mmol P m−2 d−1 and 7.2 mmol N m−2 d−1, respectively giving an N:P uptake ratio of 20:1. Thus, the elevation of nitrogen across the reef flat maintains a high N:P flux, enhancing algal growth downstream of the transect. We conclude that net community production (40 mmol C m−2 d−1) was sustained by net uptake of phosphate from the ocean and net uptake of new nitrogen from groundwater.

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The Grand Récif of Toliara (GRT) in Madagascar is a large (33 km2) barrier reef system of the SW Indian Ocean that had been well investigated in the 1960s and early 1970s. A massive degradation of the reef has been reported since at least the early 1980s, just a few years after research activities ceased in the area. Examination of historical aerial photographs and modern high-resolution remote sensing images confirms a continuous loss of coral habitat on GRT outer reef flats between 1962 and 2011, with an average loss of 65 % and a range of 37–79 % loss during this 50-year period. The usual suspects of coral community declines (cyclones, bleaching and sedimentation) may have contributed to the demise of the GRT. However, an independent study (Salimo 1997) suggests that the chronic pressure of fisherman gleaning on reef flats with destructive tools is the main driver of the observed changes. Salimo’s reported level of frequentation (6.8 fishermen per day and per km?2) and rates of destruction per fisherman (7.7 m2 of coral habitat h?1) yield a cumulated overall loss in agreement with the image-based rates of habitat loss. The GRT is unlikely to recover because this chronic stress is unlikely to decrease in the near future. Indeed, the GRT daily provides subsistence fishery resources for local Vezo people and to agriculturalist or pastoralist ethnic groups who have turned to exploiting coastal resources due to increasing aridity and dwindling agricultural and livestock production.  相似文献   
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A method for the determination of the R-(+) and S-(−) enantiomers of propranolol in blood was developed. After extraction with heptane—isopentanol and derivatization with (+)-1-(9-fluorenyl)ethyl chloroformate, excess reagent was removed using solid-phase extraction. The enantiomers were separated on an achiral, reversed-phase, radially compressed column, and detected by fluorescence with excitation and emission wavelengths of 260 and 340 nm, respectively. The limit of quantification was 0.5 ng/ml. This method was used for pharmacokinetic analysis of propranolol enantiomers after administration of immediate-release (80 mg) or sustained-release (160 mg) racemic propranolol.  相似文献   
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