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1.
Oxidation of As^Ⅲ by three types of manganese oxide minerals affected by goethite was investigated by chemical analysis, equilibrium redox, X-ray diffraction （XRD） and transmission electron microscopy （TEM）. Three synthesized Mn oxide minerals of different types, birnessite, todorokite, and hausmannite, could actively oxidize As^Ⅲ to Asv, and greatly varied in their oxidation ability. Layer structured birnessite exhibited the highest capacity of As^Ⅲ oxidation, followed by the tunnel structured todorokite. Lower oxide hansmannite possessed much low capacity of As^Ⅲ oxidation, and released more Mn^2＋ than birnessite and todorokite during the oxidation. The maximum amount of Asv produced during the oxidation of As^Ⅲ by Mn oxide minerals was in the order： birnessite （480.4 mmol/kg） 〉 todorokite （279.6 mmol/kg） 〉 hansmannite （117.9 mmol/kg）. The oxidation capacity of the Mn oxide minerals was found to be relative to the composition, crystallinity, and surface properties. In the presence of goethite oxidation of As^Ⅲ by Mn oxide minerals increased, with maximum amounts of Asv being 651.0 mmol/kg for birnessite, 332.3 mmol/kg for todorokite and 159.4 mmol/kg for hansmannite. Goethite promoted As^Ⅲ oxidation on the surface of Mn oxide minerals through adsorption of the Asv produced, incurring the decrease of Asv concentration in solutions. Thus, the combined effects of the oxidation （by Mn oxide minerals）-adsorption （by goethite） lead to rapid oxidation and immobilization of As in soils and sediments and alleviation of the As^Ⅲ toxicity in the environments.  相似文献   

2.
The shallow marine hydrothermal vents near Ambitle Island in eastern Papua New Guinea discharge hot, slightly acidic, As-rich, chemically reduced fluid into cool, slightly alkaline, oxygenated seawater. Gradients in temperature, pH, and total As (AsT), among others, are established as the two aqueous phases mix. The hydrothermal fluid contained 900 μg/L AsT, almost exclusively present as the reduced AsIII, while local seawater measured between 1.2 and 2.4 μg/L As, with approximately equal levels of AsIII and AsV. Of particular interest in this study was As speciation and abundance in pore waters as a function of sediment depth and as a function of distance from the area of focused venting. With increasing distance, AsT concentration in the pore water decreased rapidly, but remained elevated up to 300 m from the area of focused venting when compared to a non-hydrothermal control site. As a function of depth (to 100 cm) AsT concentration in the pore water profiles was elevated and generally increased with depth. Surprisingly, aqueous AsV far exceeded aqueous AsIII at almost all distances and depths investigated, while at the control site the AsIII concentration exceeded that of AsV. In the Tutum Bay hydrothermal system, chemical disequilibria among As species provide potential metabolic energy for arsenite oxidizing microorganisms where hydrothermal fluid mixes with seawater near the vent orifice, and for arsenate reducing microorganisms with increasing distance and depth from the hydrothermal point source.  相似文献   

3.
Natural attenuation of arsenic by simple adsorption on oxyhydroxides may be limited due to competing oxyanions, but uptake by coprecipitation may locally sequester arsenic. We have systematically investigated the mechanism and mode (adsorption versus coprecipitation) of arsenic uptake in the presence of carbonate and phosphate, from solutions of inorganic composition similar to many groundwaters. Efficient arsenic removal, >95% As(V) and ∼55% in initial As(III) systems, occurred over 24 h at pHs 5.5-6.5 when Fe(II) and hydroxylapatite (Ca5(PO4)3OH, HAP) “seed” crystals were added to solutions that had been previously reacted with HAP, atmospheric CO2(g) and O2(g). Arsenic adsorption was insignificant (<10%) on HAP without Fe(II). Greater uptake in the As(III) system in the presence of Fe(II) was interpreted as due to faster As(III) to As(V) oxidation by molecular oxygen in a putative pathway involving Fe(IV) and As(IV) intermediate species. HAP acts as a pH buffer that allows faster Fe(II) oxidation. Solution analyses coupled with high-resolution transmission electron microscopy (HRTEM), X-ray Energy-Dispersive Spectroscopy (EDS), and X-Ray Absorption Spectroscopy (XAS) indicated the precipitation of sub-spherical particles of an amorphous, chemically-mixed, nanophase, FeIII[(OH)3(PO4)(AsVO4)]·nH2O or FeIII[(OH)3( PO4)(AsVO4)(AsIIIO3)minor]·nH2O, where AsIIIO3 is a minor component.The mode of As uptake was further investigated in binary coprecipitation (Fe(II) + As(III) or P), and ternary coprecipitation and adsorption experiments (Fe(II) + As(III) + P) at variable As/Fe, P/Fe and As/P/Fe ratios. Foil-like, poorly crystalline, nanoparticles of FeIII(OH)3 and sub-spherical, amorphous, chemically-mixed, metastable nanoparticles of FeIII[(OH)3, PO4]·nH2O coexisted at lower P/Fe ratios than predicted by bulk solubilities of strengite (FePO4·2H2O) and goethite (FeOOH). Uptake of As and P in these systems decreased as binary coprecipitation > ternary coprecipitation > ternary adsorption.Significantly, the chemically-mixed, ferric oxyhydroxide-phosphate-arsenate nanophases found here are very similar to those found in the natural environment at slightly acidic to circum-neutral pHs in sub-oxic to oxic systems, such phases may naturally attenuate As mobility in the environment, but it is important to recognize that our system and the natural environment are kinetically evolving, and the ultimate environmental fate of As will depend on the long-term stability and potential phase transformations of these mixed nanophases. Our results also underscore the importance of using sufficiently complex, yet systematically designed, model systems to accurately represent the natural environment.  相似文献   

4.
Processing of arsenopyrite ore took place at Blackwater Au mine, New Zealand, between 1908 and 1951 and no rehabilitation was undertaken after mine closure. High As concentrations in solid processing residues (up to 40 wt% As) are due to secondary As minerals. Site pH regimes vary from 4.1 to circum-neutral. Originally, all processed As was present as arsenolite (arsenic trioxide polymorph, AsIII), a by-product of arsenopyrite roasting. Near the roaster, scorodite precipitated as a result of the high dissolved As concentration during arsenolite dissolution. The formation of scorodite has two major consequences. Firstly, the scorodite precipitate cements the ground in the vicinity of the roaster area, thereby creating an impermeable surface crust (up to 30 wt% As) and encapsulating weathered arsenolite grains within the cement. Secondly, formation of scorodite temporarily immobilizes some of the dissolved As that is generated during nearby arsenolite dissolution. Where all the available arsenolite has dissolved, scorodite becomes soluble, and the dissolved As concentrations are controlled by scorodite solubility, which is at least two orders of magnitudes lower than arsenolite solubility. Downstream Eh conditions fall below the AsV/AsIII boundary, so that scorodite does not precipitate and dissolved As concentrations are controlled by arsenolite solubility. Dissolved As reaches up to 52 mg/L in places, and exceeds the current WHO drinking water guideline of 0.01 mg/L by 5200 times. This study shows that dissolved As concentrations in discharge waters at historic mine sites are dependent on the processing technology and associated mineralogy.  相似文献   

5.
Previous studies show the importance of iron- and arsenate-reducing bacteria in mobilizing arsenic in groundwater. Here the authors present experimental evidence of arsenic mobilization in connection with bacterially mediated manganese reduction in groundwater affected by mining activities. Manganese-reducing Pseudomonas species were enriched, isolated and identified by 16S rRNA gene phylogeny from groundwater containing high co-dissolved arsenic (as AsIII) and manganese. Enrichment cultures dissolved synthetic birnessite and hausmannite efficiently, but Mn reduction by isolates was reduced at the upper range of environmental levels of dissolved AsIII. Results suggest either a self-limiting release of arsenic coupled to bacterial manganese reduction, in the absence of other electron donors like sulfide, or increased arsenic resistance conferred to Mn-reducing bacteria in consortia.  相似文献   

6.
Fresh natural montroseite of the Akouta uranium deposit (Niger) and its alteration products are characterized by reflectance measurement, X-ray diffraction pattern, chemical composition, Raman and infrared spectroscopies. Microprobe analysis allows to distinguish Fe-free and Fe-bearing montroseite. Valence measurements show mainly VIII vanadium in fresh mineral. Iron is recognized as FeII with the charge deficit compensated by VIV. A first alteration step is characterized by VIII to VIV oxidation, a second one by the FeII to FeIII oxidation. These oxidation steps are compensated by dehydrogenation inferred from water content measurements. Behaviour of hydrogen atoms during this alteration process is discussed from the I.R. spectroscopic data. Finally an evolution mechanism of the crystal structure is proposed.  相似文献   

7.
Many studies have proposed that silicic acid and phosphate (PV) can displace arsenic sorbed to iron oxides leading to elevated As concentrations in aquatic systems. While surface complexation models are adept at quantifying sorption to synthetic oxides in laboratory systems their application to complex natural systems remains challenging. In this study we provide a systematic approach to developing a robust use of models for understanding AsV distribution in natural systems in which hydrated iron oxides are the main adsorptive phase. The Waikato River provides a useful laboratory for this work because it contains high H4SiO4, AsV and PV loadings due to geothermal and agricultural inputs. A 15 min oxalate extraction and a 48 h ethylenediaminetetraacetic acid (EDTA) extraction of river sediment contained the same ratios of As:Fe, P:Fe and Si:Fe. Both of these extracts target the poorly ordered iron oxide phases (typically ferrihydrite) and by following the release of elements over time in the EDTA extraction it was possible to demonstrate that the extracted As, P, and Si were associated with the ferrihydrite. This demonstrates for the first time that a single oxalate extraction can quantify ferrihydrite sorbed H4SiO4, As and PV and provides a basis to quantify the role of these ligands in inhibiting AsV sorption to sediments. The measured concentrations of ferrihydrite sorbed AsV, PV and H4SiO4 for the Waikato River suspended sediment allow for the informed selection of appropriate model parameters for applying the Diffuse Layer Model to the system. In this way it was possible to quantify the effect of the individual components in the river water on AsV sorption. This study provides an explanation for the observation that the proportion of sorbed As in the Waikato River is generally significantly lower than that observed in rivers closer to the world average concentrations. More generally the study provides a method to quantify the role of individual water chemistry components on AsV distribution in natural systems.  相似文献   

8.
Although algal blooms, including those considered toxic or harmful, can be natural phenomena, the nature of the global problem of harmful algal blooms (HABs) has expanded both in extent and its public perception over the last several decades. Of concern, especially for resource managers, is the potential relationship between HABs and the accelerated eutrophication of coastal waters from human activities. We address current insights into the relationships between HABs and eutrophication, focusing on sources of nutrients, known effects of nutrient loading and reduction, new understanding of pathways of nutrient acquisition among HAB species, and relationships between nutrients and toxic algae. Through specific, regional, and global examples of these various relationships, we offer both an assessment of the state of understanding, and the uncertainties that require future research efforts. The sources of nutrients potentially stimulating algal blooms include sewage, atmospheric deposition, groundwater flow, as well as agricultural and aquaculture runoff and discharge. On a global basis, strong correlations have been demonstrated between total phosphorus inputs and phytoplankton production in freshwaters, and between total nitrogen input and phytoplankton production in estuarine and marine waters. There are also numerous examples in geographic regions ranging from the largest and second largest U.S. mainland estuaries (Chesapeake Bay and the Albemarle-Pamlico Estuarine System), to the Inland Sea of Japan, the Black Sea, and Chinese coastal waters, where increases in nutrient loading have been linked with the development of large biomass blooms, leading to anoxia and even toxic or harmful impacts on fisheries resources, ecosystems, and human health or recreation. Many of these regions have witnessed reductions in phytoplankton biomass (as chlorophylla) or HAB incidence when nutrient controls were put in place. Shifts in species composition have often been attributed to changes in nutrient supply ratios, primarily N∶P or N∶Si. Recently this concept has been extended to include organic forms of nutrients, and an elevation in the ratio of dissolved organic carbon to dissolved organic nitrogen (DOC∶DON) has been observed during several recent blooms. The physiological strategies by which different groups of species acquire their nutrients have become better understood, and alternate modes of nutrition such as heterotrophy and mixotrophy are now recognized as common among HAB species. Despite our increased understanding of the pathways by which nutrients are delivered to ecosystems and the pathways by which they are assimilated differentially by different groups of species, the relationships between nutrient delivery and the development of blooms and their potential toxicity or harmfulness remain poorly understood. Many factors such as algal species presence/abundance, degree of flushing or water exchange, weather conditions, and presence and abundance of grazers contribute to the success of a given species at a given point in time. Similar nutrient loads do not have the same impact in different environments or in the same environment at different points in time. Eutrophication is one of several mechanisms by which harmful algae appear to be increasing in extent and duration in many locations. Although important, it is not the only explanation for blooms or toxic outbreaks. Nutrient enrichment has been strongly linked to stimulation of some harmful species, but for others it has not been an apparent contributing factor. The overall effect of nutrient over-enrichment on harmful algal species is clearly species specific.  相似文献   

9.
Sediment cores were collected from the Neuse and Pamlico River estuaries, North Carolina, at seven different sites, and the data show strong anthropogenic influence on water quality. The sediments from these cores were dated using210Pb,137Cs,14C, and pollen horizon techniques. Specific parameters investigated include bulk density, sedimentation rates, diatom assemblage changes, nutrient and trace metal flux, and vegetation changes as recorded in the pollen record. The greatest increases in sedimentation, nutrient and metal flux and changes in diatom assemblages have occurred in the past 50–60 yr in the Pamlico and Neuse. Diatom diversity has decreased and small planktonic forms have become dominant over time, most likely due to eutrophication and increased turbidity and sedimentation. Major changes occur before phytoplankton surveys and monitoring were initiated. Overall trends are similar to those found in Chesapeake Bay, although the time frame of major changes is more recent. Dominant small planktonic diatom species differ between Chesapeake Bay and the Neuse and Pamlico. Variance in paleoecological indicators between these mid-Atlantic estuaries may be due to geomorphology and land use history.  相似文献   

10.
The effect of a 7-mo drought (La Niña 1988) was evaluated on pelagic properties in the large Patos Lagoon (30°12′–32°12′S, 50°40′–52°15′W). From December 1987 to December 1988, surface water was sampled along the longitudinal axis of the lagoon for temperature (10–29°C), salinity (0–31.4), dissolved inorganic phosphate (0.02–4.73 μM), nitrate (0.05–66.25 μM), nitrite (0.01–3.54 μM), ammonium (0.09–33.19 μM), silicate (1.11–359.20 μM), phytoplankton chlorophylla (chl; 0.4–41.2 mg m?3), primary production (gross PP 1.72–161.82 mg C m3 h?1; net PP 0.04–126.19 mg C m3 h?1), and species composition and abundance (42–4,961 ind ml?1). In the wet season the whole system acted as a river and light availability limited phytoplankton growth. During the drought from February to August monthly freshwater runoff was low and the inflow of marine water to the southern sector generated spatial variability of the analyzed properties and five functional areas were recognized. The northernmost Guaíba River (1) presented low light availability and phytoplankton chl concentration compared to the northern limnetic area (2) (chl mean 13.3 μg I?1; max 41.2 μg I?1; gross PP mean 52.6 mg C m3 h?1), which acted as a biological filter removing dissolved inorganic nutrients. Silicate concentration was strongly diminished in this area due to diatom uptake (Aulacoseira granulata, 9,330 cells ml?1). In the northern limnetic and central oligohaline (3) areas, phytoplankton biomass was controlled by light but nitrogen also played a limiting role. In the southern area (4) that is under marine influence, low chl concentration (mean 4.5 μg I?1) and gross PP (mean 28.1 mg C m3 h?1) coincided with co-limitation of nitrogen and light while the channel to the ocean (5) was strongly light limited. This study demonstrated that low light and high silicate input had a buffer effect at Patos Lagoon, hampering negative expression of cultural eutrophication. The main effect during the drought period occurred in the northern limnetic region, where low silicate values due to diatom uptake led to higher cyanobacteria abundance, and enhanced mineralization occurred in the central oligohaline lagoon. Increased rainfall resulted in light limitation and decreasing primary production in the entire freshwater lagoon, and the adjacent coastal region benefited from nutrient enrichment.  相似文献   

11.
Enteromorpha intestinalis is a bloom-forming species of macroalgae associated with eutrophication. The objective of this study was to investigate how this alga performs osmoregulation and nutrient uptake in order to proliferate under environmental conditions that covary with eutrophication. We quantified the response ofE. intestinalis to salinity, light, and nutrients. We performed two short-term (48 h) laboratory experiments (salinity alone and salinity × nutrients × light) to examine the algal responses of tissue water, potassium (K+), and nutrient (NO 3 − and total N) content. Tissue water content decreased with increasing salinity, and although K+ concentration decreased from the initial concentration, it decreased less with increased salinity treatment demonstrating two mechanisms to withstand short-term salinity fluctuation. The salinity × nutrient × light experiment showed that, in the short term, light had an interaction with tissue K+. Total tissue N content was positively related to N treatment level, and light did not affect total nutrient concentration. The effect of light was present whether the nutrients were present in the tissue as inorganic or organic forms. With reduced light, we hypothe size that the assimilation of inorganic to organic N was energy limited. The ability of this alga to take up available nutrients rapidly for growth and short-term osmoregulation, even under low light and salinity levels, helps to explain the bloom potential ofE. intestinalis.  相似文献   

12.
Chromium (Cr) is a heavy metal that exists in soils in two stable oxidation states, +III and +VI. The trivalent species is an essential nutrient, whereas the hexavalent species is highly toxic. This study investigated the environmental impact of CrIII potentially released into soil from wastes and various materials by determining the risk of oxidation of initially soluble inorganic CrIII into hazardous CrVI. The principal aim was to describe the pH-dependent mechanisms that regulate 1) the formation of CrVI from the easily soluble CrIII and 2) the potential bioavailability of CrIII and that of CrVI species produced in the oxidation of CrIII in agricultural soil (fine sand, organic carbon 3.2%). The amount of CrVI formed in oxic soil conditions was regulated by two counteracting reactions: 1) oxidation of CrIII into CrVI by manganese oxide (MnIVO2) and 2) the subsequent reduction of CrVI by organic matter back to CrIII. The effect of pH on this net-oxidation of CrIII and on the chemical availability of both CrIII and CrVI species was investigated in soil samples incubated with or without excessive amounts of synthetic MnO2, over the chemically adjusted pH range of 3.9–6.3 (+22 °C, 47 d). In soil subsamples without added MnO2, the net-oxidation of CrIII into CrVI (1 mM CrCl3 in soil suspensions, 1:10 w/V) was negligible. As for the MnO2-treated soils, at maximum only 4.7% of added CrIII was oxidized – regardless of the high oxidation potential of these subsamples. The lowest production of CrVI was observed under acidic soil conditions at pH ∼4. At low pH, the net-oxidation diminished as result of enhanced reduction of CrVI back to CrIII. At higher pHs, the oxidation was limited by enhanced precipitation (or adsorption) of CrIII, which lowered the overall amount of CrIII susceptible for oxidation. Moreover, the oxidation reactions by MnO2 were inhibited by formation of Cr(OH)3 coverage on its surface. The pH-dependent chemical bioavailability of added CrIII differed from that of the CrVI formed. At elevated pHs the chemical availability of CrIII decreased, whereas that of CrVI produced increased. However, the risk of CrVI formation through oxidation of the easily soluble inorganic CrIII was considered to be low in agricultural soils high in organic matter and low in innate MnO2.  相似文献   

13.
The composition and structure of aktashite from the Aktash deposit, Gorny Altai, Russia, have been studied by electron microprobe and X-ray structural analysis. On the basis of close compositions and crystal structures, the identity of aktashite from the Gal-Khaya and Aktash deposits has been demonstrated. Crystals of aktashite are of trigonal symmetry; the unit-cell dimensions are: a = 13.7500(4), c = 9.3600(3) Å, V = 532.54(8) Å3, space group R3, Z = 3 for the composition of Cu6Hg3As4S12, R = 0.043. The structure of aktashite as a framework of vertex-shared HgS4? and CuS4? tetrahedrons of the same orientation is intimately related to the sphalerite-type structure. The earlier identified uncommon cluster group [As4] has been verified and its parameters have been refined. It is shown that the structure may be represented as construction blocks (As4S12)12? packed according to the law of the distorted cubic I-cell.  相似文献   

14.
The 13C/12C ratio of carbon compounds is used to identify sources and sinks in the global carbon cycle. However, the relatively enriched 13C content observed for marine organic carbon remains enigmatic. The majority of oceanic carbon is fixed by algae and cyanobacteria via the Calvin-Benson-Bassham cycle, yet isotopic discrimination by the CO2 fixation enzyme, RubisCO (ribulose 1,5-bisphosphate carboxylase/oxygenase), has only been measured for a single marine cyanobacterium. Different forms of RubisCO occur in different phytoplankton species (overall amino acid identity varying by as much as ∼75%) and thus may vary in the degree to which they fractionate carbon. Here we measured isotope discrimination by RubisCO from the coccolithophore Emiliania huxleyi, a cosmopolitan species used as a marine algal model.E. huxleyi RubisCO discriminated substantially less (ε = 11.1‰) against 13CO2 than other RubisCO enzymes (18-29‰), despite having Michaelis-Menten kinetic parameters (KCO2 = 72 μM; Vmax = 0.66 μmol min−1 mg−1 protein) similar to those measured for RubisCO enzymes from different organisms. If widespread, decreased isotope discrimination of 13C by phytoplankton RubisCO may be a major factor influencing the enriched 13C content of marine organic carbon. This finding emphasizes the necessity of (a) determining ε values for RubisCOs of other marine phytoplankton and (b) re-evaluation of δ13C values from physiological, environmental, and geological studies.  相似文献   

15.
While many coastal ecosystems previously supported dense meadows of seagrass and dense stocks of bivalves, the impacts of overfishing, eutrophication, harmful algal blooms, and habitat loss have contributed to the decline of these important resources. Anthropogenic nutrient loading and subsequent eutrophication has been identified by some researchers as a primary driver of these losses, but others have described potential positive effects of eutrophication on some estuarine resources. The Peconic Estuary, Long Island, NY, USA, offers a naturally occurring nutrient-loading gradient from eutrophic tidal creeks in its western reaches to mesotrophic bays in the eastern region. Over 2 years, we conducted an experiment across this gradient to examine the effects of eutrophication on the growth of estuarine species, including juvenile bivalves (northern quahogs (Mercenaria mercenaria), eastern oysters, (Crassostrea virginica), and bay scallops (Argopecten irradians)) and slipper limpet (Crepidula fornicata). Water quality and phytoplankton community biomass and composition were concurrently monitored at each site, and the effects of these variables on the growth of estuarine species were analyzed with multiple regression model. Eutrophication seemed to impact shellfish through changes in the quality of food and not the quantity since the growth rates of shellfish were more often correlated with densities of specific cell types or quality of seston rather than bulk measures of phytoplankton and organic seston. Northern quahogs and eastern oysters grew maximally within eutrophic locales, and their growth was positively correlated with high densities of autotrophic nanoflagellates and centric diatoms in these regions (p?<?0.001). The growth rates of northern quahogs were also positively correlated with relative water motion, suggesting an important role for tidal currents in delivering seston to suspension feeders. Bay scallops and slipper limpets were negatively impacted by eutrophication, growing at the slowest rate at the most eutrophic sites. Furthermore, bay scallop growth was negatively correlated with densities of dinoflagellates, which were more abundant at the most eutrophic site (p?<?0.001). These results suggest that nutrient loading can have significant but complex effects on suspension-feeding molluscs with select species (e.g., oysters and clams) benefiting from eutrophication and other species performing poorly (e.g., scallops and slipper limpets). Future management approaches that seek to restore bivalve populations will need to account for the differential effects of nutrient loading as managers target species and regions to be restored.  相似文献   

16.
The rates of photosynthetic carbon fixation for some natural populations of Chesapeake Bay phytoplankton and for unialgal cultures of species isolated from those populations follow hyperbolic saturation kinetics with respect to total inorganic carbon concentrations. The apparent half-saturation constants, Kc, measured by 14C uptake are close to and in some cases larger than ambient concentrations of total inorganic carbon, indicating that inorganic carbon can be a limiting nutrient in eutrophic systems. Addition of bicarbonate ion to incubation bottles increased the measured 14C uptake rates by factors as high as 2.5 for natural samples and 4.5 for laboratory cultures.  相似文献   

17.
An experimental in situ microcosm study was conducted in the tropical lagoon La Mancha (Gulf of Mexico) to determine whether or not nutrient limitation occurs and to examine the direct effect of an inorganic nutrient pulse on the phytoplankton community structure. The phytoplankton community response to the addition of four treatments with different combinations of nitrogen (N), phosphorus (P), and silica (Si) (+N-NH4 +, +P-PO4 ?, +Si-SO3, and N:P16) showed that phytoplankton was N-limited as indicated by an increase in phytoplankton biomass (i.e., chlorophyll a) (range, 8–34 mg m?3) during the dry season in two consecutive years (2006 and 2007). Picophytoplankton abundance significantly increased in the +N treatment (145.46 103 cells L?1), while microphytoplankton reached a maximum abundance (68.38 103 cells L?1) in the N:P16 treatment. Phytoplankton composition changed from a community initially dominated by dinoflagellates (e.g., Prorocentrum spp.) to another dominated by diatoms (Thalassiosira and Nitzschia longissima) in the N:P16 treatment. The +N treatment significantly increased Synechococcus sp. growth rates (1.3 divisions per day) (picocyanobacteria). Biomarker pigments measured in the experimental microcosms confirmed observed changes in phytoplankton groups. Our results reveal that La Mancha lagoon is a N-limited coastal system during the dry season and provides evidence of the temporal species successional patterns and mechanisms regulating the phytoplankton community response to nutrient enrichment pulses in this already eutrophic coastal lagoon.  相似文献   

18.
Data were collected in the Tagus estuary from 1999–2007 on a monthly basis and combined with published results and for several previous years between 1980 and 1995, so that a comprehensive analysis could be performed over a non-continuous 27-year period. Sampling conditions and methods were similar for all datasets. Extreme wet and dry years were observed. River flow was strongly linked to phytoplankton abundance, with the highest biomass attained in dry years. The observed range of annual median Chl a was 1.8–7.6 µg L?1 and the overall median was 3.5 µg L?1. Dissolved inorganic nitrogen (DIN) and silicate showed a clear seasonal pattern, with a maximum in winter?spring, indicating a freshwater origin. Although wastewater treatment started in 1990, no difference was detected from 1980 to the present in terms of DIN and phosphorus. The recorded seasonal pattern for biomass with highest values in late spring–summer period is comparable to other temperate tidally influenced ecosystems. In spite of interannual differences in terms of Chl a concentration or the time of the maximum Chl a occurrence, a repeatable pattern could be identified. The mean growth development time for phytoplankton was 163 days (June 12) ranging 129–206 days (May 9–July 26) during the sampling period. No obvious changes in phytoplankton community structure were observed over time: diatoms were always the dominant group, and cryptophytes were relatively abundant throughout autumn–winter. The dominant species have remained essentially the same since 1969. River inflow, light availability, and temperature were the major factors shaping phytoplankton variability patterns. The strong influence of tidal mixing on the estuarine waters appears to lower the risk of potential eutrophication in the Tagus estuary. The lack of change in nutrients and phytoplankton biomass and composition observed in this study is an important contribution towards the assessment of natural variability versus responses to man-induced inputs in this severely anthropogenically disturbed estuary.  相似文献   

19.
Lammerite-β, Cu3(AsO4)2, occurs as a product of the post-eruption fumarole activity of the second cinder cone of the North breach of the Great Fissure Tolbachik eruption in 1975–1976, Kamchatka Peninsula, Russia. Sporadic light to dark green splinter-shaped grains are no larger than 0.15 mm in size. Cleavage is not observed. The mechanical admixture of finely dispersed hematite forms condensed brownish spots that are occasionally zonal relative to the contours of the lammerite-β grains. Associated minerals are euchlorine, piypite, alumoklyuchevskite, alarsite, and lammerite. Lammerite-β is brittle and transparent and has vitreous luster. The calculated density is 5.06 g/cm3. The mineral is not pleochroic, biaxial (+), α = 1.887(5), β = 1.936(5), γ = 2.01(1), 2V(calc.) = 80.9°; dispersion is strong, r < v. The new mineral is monoclinic, the space group is P21/c, a = 6.306(1), b = 8.643(1), c = 11.310(1) Å, β = 92.26(1)°, V = 615.9(1) Å3, and Z = 4. Characteristic reflections in the X-ray powder diffraction pattern (I-d-hkl) are 100-2.83-004, 10-5.65-002, and 10-4.32-020. The chemical composition is as follows, wt %: 51.30 CuO, 0.32 ZnO, 49.12 As2O3, with a total of 100.74 wt %. The empirical and idealized formulas are Cu3.00Zn0.02As1.99O8 and Cu3(AsO4)2, respectively.  相似文献   

20.
海洋浮游植物对磷的响应研究进展   总被引：3，自引：0，他引：3  
磷是海洋浮游植物赖以生存的一种必需营养元素.海洋浮游植物对磷的响应,与初级生产力、碳循环以及固氮作用密切相关.总结了浮游植物可利用的磷源:优先吸收溶解无机磷;在寡磷海域,可通过相关酶类协助利用溶解有机磷来抵御无机磷的缺乏.对比了不同种类浮游植物对不同形态磷源利用方式的差异并从浮游植物生理学角度阐述了存在差异的根本原因.探讨了浮游植物对低磷环境的响应机制.近期的研究发现浮游植物细胞表面可以吸附磷,该发现有利于更加准确地衡量浮游植物承受的营养盐限制问题,进一步完善对海洋磷储库及其生物地球化学循环的认识.最后提出了今后需进一步研究的关键科学问题:浮游植物细胞表面吸附磷的机制;对不同结构有机磷化物的利用机理;浮游植物对磷的海洋生物地球化学循环的响应及反馈作用.  相似文献   

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