共查询到20条相似文献，搜索用时 15 毫秒
1.
O.R. Chaparro Y.A. Montiel C.J. Segura V.M. Cubillos R.J. Thompson J.M. Navarro 《Estuarine, Coastal and Shelf Science》2008,76(4):861-868
The suspension-feeding gastropod Crepipatella dilatata occurs in estuaries in southern Chile that experience considerable fluctuations in salinity, driven by tidal and atmospheric forces. In the Quempillén estuary salinities as low as 9 psu may occur after severe rainstorms, and persist for several hours. In this study salinity was the major factor influencing the clearance rate of C. dilatata. At salinities below 20 psu, filtration ceased, whereas at high salinities (>22 psu) mean clearance rate was 0.24 l h−1 standard animal−1 (S.D. 0.18) for actively filtering individuals. This was confirmed by laboratory experiments under controlled conditions. Endoscopic observations were consistent with measurements of clearance rate, and showed that at salinity 25–30 psu the rate of transport along the gill filaments of particulate material embedded in mucus was 759 μm s−1 (S.D. 480), but particle transport ceased at and below salinity 20 psu. Complete or partial isolation of the mantle cavity from the environment may be a mechanism to protect soft tissues and/or incubated egg capsules from osmotic stress. 相似文献
2.
可口革囊星虫(Phascolosoma esculenta)重组铁蛋白富集Pb2+等重金属特性和功能研究 总被引：1，自引：1，他引：0
利用可口革囊星虫重组铁蛋白富集Pb2+、Fe3+、Cd2+、Cr3+、Cu2+、Mn2+、Sn2+和Zn2+等8 种重金属离子后, 通过透射显微镜和傅里叶红外光谱测定蛋白的超微结构变化和内部基团特性。以 天然的马脾铁蛋白为对照, 观察重组铁蛋白与天然铁蛋白的差别。结果显示, 重组铁蛋白富集Pb2+ 和其它7 种重金属离子后蛋白体积大小与重金属离子种类直接相关。重组铁蛋白相对天然铁蛋白来 说在富集不同种类重金属离子后, 除了非特异性酰胺特征峰和蛋白特征峰外, 还出现一些专门富集 某些重金属离子的特异基团, 如:-CH3、-CH2-、-CH-、-NH-、-SO3-、-COOH、-S=S-和-C-S-C 等。 通过细胞实验进一步验证了铁结合蛋白能够通过富集重金属离子Pb2+来保护小鼠成骨前体细胞 MRC3T3-E1, 使细胞的死亡率明显降低(P<0.05). 相似文献
3.
Andrew P. L. Cheung Timothy H. -J. Lam King Ming Chan 《Marine environmental research》2004,58(2-5):389
Tilapia is a common fish species inhabiting inland waters and estuarine regions in Hong Kong and Southeast Asia, and useful for bio-monitoring of metal pollution. Metallothionein (MT) gene expression in fish tissues has been useful to sub-lethal risk assessment as biomarker of exposure to metal ions in fishes inhabiting metal contaminated area. To investigate metal inductions of Tilapia MT gene expression in vivo, Tilapias were injected with different concentrations of heavy metals and tissues were then removed for quantitative PCR assay using mimic PCR methods. All of the metal ions tested (Cu2+, Cd2+, Hg2+, Ni2+, Pb2+ and Zn2+) were able to induce hepatic MT mRNA levels. Renal MT mRNA levels of Cd2+ and Zn2+ treated fish was not induced with significant fold induction, however MT mRNA levels in gills were sensitive to the administrations of these metal ions. These data indicated that Tilapia MT mRNA levels in gills and liver are sensitive biomarker of exposure to various metal ions. 相似文献
4.
Pasquale Crea Concetta De Stefano Demetrio Milea Silvio Sammartano 《Marine Chemistry》2008,112(3-4):142-148
The results of a potentiometric investigation (by ISE-H+, glass electrode) on the speciation of phytate ion (Phy12−) in an ionic medium simulating the major components (Na+, K+, Ca2+, Mg2+, Cl− and SO42−) of natural seawater, at different salinities and t = 25 °C, are reported. The work was particularly aimed at determining the possible formation of mixed Ca2+–Mg2+–phytate ion pairs, and to establish how including the formation of these mixed species would affect the speciation modeling in seawater media. After testing various speciation models, that considering the formation of the MgCaH3Phy5−, MgCaH4Phy4−, Mg2CaH3Phy3− and Mg2CaH4Phy2− species was accepted, and corresponding stability constants were determined at two salinities (S = 5, 10). A discussion is reported both on the choice of the experimental conditions and on the possibility to extend these results to those typical of real seawater. A detailed procedure is also described to demonstrate that the stability of these species is higher than that statistically predicted. As reported in literature, a parameter, namely log X, has been determined in order to quantify this extra stability for the formation of each mixed species at various salinities. For example, at S = 10, log X113 = 2.67 and log X114 = 1.37 for MgCaH3Phy5− and MgCaH4Phy4− (statistical value is log Xstat = 0.60), and log X213 = 6.11 and log X214 = 2.15 for Mg2CaH3Phy3− and Mg2CaH4Phy2− (log Xstat = 1.43), respectively. Results obtained also showed that the formation of these species may occur even in conditions of low salinity (i.e. low concentration of alkaline earth cations) and low pH (i.e., more protonated ligand). 相似文献
5.
Cd~(2+)对青蛤(Cyclina sinensis)的毒性及蓄积过程研究 总被引：2，自引：0，他引：2
利用水生动物急性毒性实验方法,在6个浓度下Cd2+对青蛤的急性毒性进行测定,经回归分析后,得到Cd2+对青蛤96h半致死浓度为20.09mg/L,安全浓度为0.201mg/L。分别对半致死浓度和安全浓度下Cd2+在青蛤体内不同组织的蓄积情况进行了分析。结果表明,在半致死浓度条件下,168h青蛤各组织Cd2+的含量依次为肌肉内脏团鳃;而在安全浓度下,其结果为内脏团鳃肌肉,内脏团对于Cd2+富集能力远高于肌肉。讨论了青蛤的养殖环境及产品检验等问题。 相似文献
6.
7.
Cd2+和Cu2+对泥蚶的急性毒性和联合毒性试验 总被引：1，自引：0，他引：1
为了解重金属Cd2+和Cu2+对泥蚶的毒害程度和泥蚶对重金属Cd2+和Cu2+的解毒能力,用毒理学实验方法研究了Cd2+和Cu2+对泥蚶(Tegillarca granosa)的急性毒性和联合毒性效应。结果表明:Cd2+、Cu2+对泥蚶的96 h半致死质量浓度分别为6.189、0.460 mg/L;安全质量浓度分别为0.062、0.005 mg/L;相对毒性Cu2+Cd2+。在1︰1毒性单位的联合作用下,Cd2+和Cu2+对泥蚶96 h的半致死质量浓度分别为1.984、0.147 mg/L;安全质量浓度分别为0.020、0.001 mg/L。2种重金属离子的联合毒性大于任一重金属离子的毒性,联合毒性表现为协同作用。 相似文献
8.
陈贞奋 《海洋学报(英文版)》1986,5(4):614-625
Chaetoceros muelleri Lemmermann was cultured in solution of different concentrations of Cu2 , Pb2 , Zn2 and Cd2 , and in mixtures of any two of them. After 6 days the effect of these heavy metal cations on the growth rate and chlorophyll contents of the diatom were determined and an Opton microscope was used to observe the morphology and size of the cells.The experimental results show that the effects of toxicity of these four heavy metals on Chaetoceros muelleri are: Cu2 >Pb2 >Zn2 >Cd2 . However, the cells did not differ significantly in their morphology and size from the controled ones.In any of the mixed metals cultures, its growth rate came close to and was higher than that of the single metal culture of higher concentration. 相似文献
9.
The distribution coefficient (λMg) of Mg2+ ions between calcite and solution was found to be 0.012 ± 0.001 (10°C), 0.014 ± 0.001 (15°C), 0.019 ± 0.001 (25°C), 0.024 ± 0.001 (30°C), 0.027 ± 0.001 (35°C) and 0.040 + 0.003 (50°C). This indicates a remarkable dependence on temperature. The effect of the Mg2+/Ca2+ molar ratio in a parent solution on λMg for calcite is small, where the molar ratio lies in the range 0.04-2. However, the λMg value for aragonite tends to decrease with increasing Mg2+/Ca2+ ratio in the parent solution. The largest Mg content of calcite in the Ca(HCO3)2-Mg2+ → calcite system is around 2 mol% in the temperature range 10–50°C. Neither homogeneous nor heterogeneous distribution laws hold for aragonite precipitation, and the temperature effect on the coprecipitation of Mg2+ ions with aragonite is very small. 相似文献
10.
Aymeric Dabrin Jrg Schfer Grard Blanc Emilie Strady Matthieu Masson Ccile Bossy Sabine Castelle Naïg Girardot Alexandra Coynel 《Estuarine, Coastal and Shelf Science》2009,84(4):429-439
Dissolved Cd (CdD) concentrations along the salinity gradient were measured in surface water of the Gironde Estuary during 15 cruises (2001–2007), covering a wide range of contrasting situations in terms of hydrology, turbidity and season. During all situations dissolved Cd concentrations displayed maximum values in the mid-salinity range, reflecting Cd addition by chloride-induced desorption and complexation. The daily net CdD fluxes from the Gironde Estuary to the coastal ocean were estimated using Boyle's method. Extrapolating CdD concentrations in the high salinity range to the freshwater end member using a theoretical dilution line produced 15 theoretical Cd concentrations (CdD0), each representative of one distinct situation. The obtained CdD0 concentrations were relatively similar (201 ± 28 ng L−1) when freshwater discharge Q was >500 m3 s−1 (508 ≤ Q ≤ 2600 m3 s−1), but were highly variable (340 ± 80 ng L−1; 247–490 ng L−1) for low discharge situations (169 ≤ Q ≤ 368 m3 s−1). The respective daily CdD net fluxes were 5–39 kg day−1, mainly depending on freshwater discharge. As this observation invalidates the existing method of estimating annual CdD net fluxes, we proposed an empirical model, using representative CdD0 values and daily freshwater discharges for the 2001–2007 period. Subsequent integration produced reliable CdD net flux estimates for the Gironde Estuary at the annual timescale that ranged between 3.8–5.0 t a−1 in 2005 and 6.0–7.2 t a−1 in 2004, depending on freshwater discharge. Comparing CdD net fluxes with the incoming CdD fluxes suggested that the annual net CdD addition in the Gironde Estuary ranged from 3.5 to 6.7 t a−1, without any clear temporal trend during the past seven years. The annual CdD net fluxes did not show a clearly decreasing trend in spite of an overall decrease by a factor 6 in Cd gross fluxes during the past decade. Furthermore, in six years out of seven (except 2003), the annual CdD net fluxes even exceeded river borne total (dissolved + particulate) gross Cd fluxes into the estuary. These observations were attributed to progressive Cd desorption from both suspended particles and bottom sediment during various sedimentation–resuspension cycles induced by tidal currents and/or continuous dredging (navigation channel) and diverse intra-estuarine sources (wet deposition, urban sources, and agriculture). Provided that gross fluxes remain stable over time, dissolved Cd exportation from the Gironde Estuary to the coastal ocean may remain at the present level for the coming decade and the estuarine sedimentary Cd stock is forecast to decrease slowly. 相似文献
11.
The extent and mechanisms of adsorption of marine pore water organic matter to montmorillonite were studied in a series of batch and sequential adsorption experiments. Pore water natural organic matter (pNOM) and easily extracted natural organic matter (eNOM) were collected from Liberty Bay (Puget Sound, WA, USA) sediments. The pNOM and eNOM were each divided into two size fractions using a 1000 D ultrafilter. Batch adsorption isotherms were approximately linear, and the >1000 D fractions of both pNOM and eNOM had larger partition coefficients (Kd) than the <1000 D fractions. A two-component fit of the sequential adsorption data indicated that pNOM and eNOM contained a similar amount of NOM (30%) that was not surface reactive toward montmorillonite. After correcting the batch adsorption Kds for the non-reactive components, the Kds estimated by batch and sequential adsorption were identical (2.7 l/kg for >1000 D pNOM and eNOM, and 1.6 l/kg for <1000 D pNOM and eNOM). Mechanisms of adsorption were investigated by systematically changing conditions (pH, temperature and ionic composition) of >1000 D fractions during batch isotherm experiments. Adsorption of NOM was found to decrease with increased temperature, suggesting that hydrophobic effects were not the dominant adsorption mechanisms in this system. Ion exchange was also not an important adsorption mechanism because adsorption increased with ionic strength. The observed enhancement in adsorption with ionic strength indicated that van der Waals interactions were important in the adsorption of NOM. Ligand exchange was found to be a significant mechanism since the presence of SO42− in solution reduced the amount of NOM adsorbed. Ca2+ enhanced adsorption slightly more than Na+, suggesting that cation bridging was involved. The relative contributions of van der Waals interactions, ligand exchange and cation bridging were estimated to be approximately 60%, 35% and 5%, respectively, for adsorption of NOM in a CaCl2 solution. 相似文献
12.
采用实验生态学方法,研究了Cd~(2+)-Cu~(2+)单一及复合胁迫3d、6d、9d对双齿围沙蚕(Perinereis aibuhitensis)消化酶活性和抗氧化指标的影响。结果表明,沙蚕的各项不同指标对Cd~(2+)、Cu~(2+)胁迫的响应表现出不同的变化趋势,复合胁迫中Cd~(2+)-Cu~(2+)对沙蚕各指标的影响存在交互效应。沙蚕3种消化酶活性大小为淀粉酶蛋白酶脂肪酶。Cd~(2+)、Cu~(2+)单一胁迫能激发沙蚕淀粉酶活性,激发作用强于复合胁迫。Cd~(2+)、Cu~(2+)单一胁迫实验前期低浓度组蛋白酶被抑制,高浓度组被诱导,复合胁迫实验前期Cd~(2+)-Cu~(2+)对蛋白酶活性的影响存在协同作用。Cd~(2+)、Cu~(2+)胁迫对沙蚕脂肪酶活性整体表现出抑制作用。Cd~(2+)、Cu~(2+)胁迫诱导沙蚕超氧化物歧化酶(SOD),整体上激活过氧化氢酶(CAT)活性。Cd~(2+)单一胁迫实验组过氧化物酶(POD)均被显著诱导,具有"剂量-效应"关系,Cu~(2+)单一胁迫实验后期POD被显著诱导,复合胁迫实验中,低浓度Cu~(2+)组POD被显著诱导,高浓度Cu~(2+)组POD被显著抑制。实验组沙蚕谷胱甘肽过氧化物酶(GXH-Px)活性和丙二醛(MDA)含量均高于对照组,复合胁迫实验前期,GXH-Px活性与Cu~(2+)浓度呈正相关关系,与Cd~(2+)浓度呈负相关关系。显著的效应-剂量间相关关系存在于特定时间(3d、6d)的MDA含量,沙蚕MDA含量用作监测海洋重金属污染的生物标志物的可能性较大。 相似文献
13.
Dissolved and particulate manganese in seawater samples derived from the English Channel has been analyzed using graphite furnace atomic absorption (GFAAS), and inductively coupled plasma atomic emission (ICP—AES) spectroscopies. Because of the high contents of carbonate minerals found in the suspended matter samples, the English Channel constitutes an ideal field area for the study of the Mn2+/Ca2+/CaCO3 system. Owing to the chemical speciation of particulate manganese and the combined use of the X-ray diffraction and electron spin resonance spectroscopy we have shown the importance of the carbonate phase in the stabilization of manganese (II). This has been confirmed by p-pH measurements in the field. All these studies have also indicated that: (1) manganese is associated with calcite in the form of a solid solution, MnxCa1−xCO3; and (2) significant increases in the concentrations of particulate manganese, especially in offshore waters, occur in summer. This seasonal phenomenon has been attributed to the proliferation of coccolithophorids, which are known to be covered with calcified skeletons at high specific surface areas. To appraise the implication of the coccolithophorid-blooms phenomenon on the Mn2+/Ca2+/CaCO3 system, we have used the manganese distribution coefficient, Di, between the liquid phase and CaCO3 particles. Overall we have shown that: (1) Di in summer (i.e. when coccoliths considered as very fine-grained calcite are abundant) is much higher than that obtained in winter; and (2) in the vicinity of the French coast, Di does not vary significantly even in summer. This is because of the high content of chalk-derived particles found in the near-shore waters. 相似文献
14.
The purpose of the present study was to elucidate in vitro effects of Hg2+, Zn2+, Ni2+ and Cd2+ on cytochrome P4501A1 (CYP1A1) dependent EROD activities in leaping mullet liver microsomes. Fish captured from the most polluted part of Izmir Bay, had highly elevated EROD activities, and induced CYP1A1 protein levels as determined by Western blotting. Although all of the metal ions caused inhibition of the initial velocity of the reaction, Hg2+ and Cd2+ exhibited much higher inhibitory effect at lower concentrations and they were evidently more potent inhibitors than others. The inhibitor concentration giving 50% inhibition (IC50 values) of Zn2+, Ni2+, Cd2+ and Hg2+ of initial EROD activity were 107, 16, 1.3 and 0.15 micromolar, respectively. Glutathione (GSH) at 0.5 mM final concentration, completely reversed Ni2+ and Cd2+ inhibition of EROD activity indicating the protective action of GSH. 相似文献
15.
G. V. Novikov O. Yu. Bogdanova M. E. Melnikov N. V. Lobus A. N. Drozdova N. A. Shulga 《Oceanology》2016,56(1):65-69
The behavior of heavy-metal cations in ore minerals of cobalt-rich ferromanganese crusts from the Marcus Wake seamount in aqueous solutions of metal salts was studied in experiments. The Zn2+ and Cd2+ cations showed high reactivity and Ва2+ and Pb2+ showed low reactivity. It was found that Zn2+ and Cd2+ cations within the ore mineral composition are mainly absorbed (up to 66%) whereas Pb2+ and Ва2+ are chemically bound (up to 70%). Ore minerals in the crusts are characterized by sorption properties and high ionexchange capacity by these cations (1.94–2.62 mg-equiv/g). The capacity values by heavy-metal cations for ore minerals of the crusts from different areas of the Marcus Wake seamount are close to each other. 相似文献
16.
采用静态急性毒性实验研究了重金属Pb~(2+)对青蛤(Cyclina sinensis)的生物急性毒性效应,测定了在96 h Pb~(2+)半致死浓度的1/10(TC组)和1/100(SC组)两个浓度胁迫下,血淋巴液中酸性磷酸酶(ACP)、碱性磷酸酶(AKP)和溶菌酶(LSZ)活性的变化。结果显示:Pb~(2+)的96 h LC50为7.938 mg/L; SC组ACP活性表现为诱导-抑制趋势,除4 d外均与对照组差异显著(P0.05), TC组为抑制趋势,为3个组中的最低,与对照组差异显著(P0.05);实验组SC组和TC组的AKP、LSZ活性均表现为前期为诱导中后期受抑制的趋势,与对照组差异显著(P0.05),且TC组活性始终低于SC组,表现出Pb~(2+)的胁迫浓度越高酶活性受到的抑制作用越大。以上结果表明,重金属Pb~(2+)对青蛤的毒性级别为高毒级,能造成青蛤免疫相关酶的活性受到抑制,影响青蛤的免疫能力,而且这种抑制作用随着环境中Pb~(2+)浓度增加而增加。 相似文献
17.
1. The adsorption action of basic zinc carbonate adsorbent on uranium in natural seawater can be expressed with the following formula of adsorption isotherm:C=k(U*)n = 8.51× 10-1(U*)0.49,where C is the concentration of uranium on adsorbent; U* is content of uranium in natural seawater employed.2. when the quantity of basic zinc carbonate adsorbent (T) is constant, with the increase of natural seawater quantity through the adsorption column (G), also increased are the adsorption content of uranium of the adsorbent (U), the concentration of uranium on the adsorbent (C) and the concentration of residual uranium (C0*) in natural seawater after adsorbing uranium, while the rate of recovery of uranium (R) is decreased. With the increase of (G) the coefficient of distribution (Kd) decreases to a certain value and then a little rises again. 相似文献
18.
The interaction of Mn2+ with the surface of calcite in aqueous solutions is complex. In dilute solutions the Mn2+ is rapidly absorbed, MnCO33 nucleates on the calcite surface and then grows by a first order reaction with respect to the initial Mn2+ concentration. At higher ionic strengths in NaCl solutions, the rate of these processes is slower, but the same general pattern persists. In solutions containing Mg2+, at the concentration of seawater and in seawater, the nucleation phase of the uptake process does not appear to occur. The long-term uptake rate of Mn2+ on the surface of calcite in seawater is first order with respect to the dissolved Mn2+ concentration. The rate constant is over three orders of magnitude smaller than that found in dilute Mg2+-free solutions. A probable explanation for the slower growth rate in seawater is that MnCO3 is not nucleated on the calcite surface due to the presence of high Mg2+ concentrations. The Mg2+, through site competition, prevents enough Mn2+ from being adsorbed to reach a critical concentration for MnCO3 nucleation. This behavior is similar to that found for orthophosphate with calcite surfaces in dilute solutions and seawater. It indicates that rhodochrosite cannot nucleate in carbonate-rich recent sediments unless the Mg2+ concentration is lowered below that of seawater.Measurements of the solubility of rhodochrosite in seawater gave results from an undersaturation approach to equilibrium in excellent agreement with those found in previous studies in dilute solutions. When equilibrium was approached from supersaturation, approximately fifty times more calcium was precipitated than Mn2+. The measured solubility was over twice that determined from undersaturation. It is possible that a Mn—calcite containing 25 to 30 mol% MnCO3 formed on the rhodochrosite from the supersaturated solutions. Consequently, it is doubtful that pure rhodochrosite controls the concentration of Mn2+ even in calcium carbonate-poor marine environments. 相似文献
19.
Ursula Werner Anna Blazejak Paul Bird Gabriele Eickert Raphaela Schoon Raeid M.M. Abed Andrew Bissett Dirk de Beer 《Estuarine, Coastal and Shelf Science》2008,76(4):876-888
We investigated microphytobenthic photosynthesis at four stations in the coral reef sediments at Heron Reef, Australia. The microphytobenthos was dominated by diatoms, dinoflagellates and cyanobacteria, as indicated by biomarker pigment analysis. Conspicuous algae firmly attached to the sand grains (ca. 100 μm in diameter, surrounded by a hard transparent wall) were rich in peridinin, a marker pigment for dinoflagellates, but also showed a high diversity based on cyanobacterial 16S rDNA gene sequence analysis. Specimens of these algae that were buried below the photic zone exhibited an unexpected stimulation of respiration by light, resulting in an increase of local oxygen concentrations upon darkening. Net photosynthesis of the sediments varied between 1.9 and 8.5 mmol O2 m−2 h−1 and was strongly correlated with Chl a content, which lay between 31 and 84 mg m−2. An estimate based on our spatially limited dataset indicates that the microphytobenthic production for the entire reef is in the order of magnitude of the production estimated for corals. Photosynthesis stimulated calcification at all investigated sites (0.2–1.0 mmol Ca2+ m−2 h−1). The sediments of at least three stations were net calcifying. Sedimentary N2-fixation rates (measured by acetylene reduction assays at two sites) ranged between 0.9 to 3.9 mmol N2 m−2 h−1 and were highest in the light, indicating the importance of heterocystous cyanobacteria. In coral fingers no N2-fixation was measurable, which stresses the importance of the sediment compartment for reef nitrogen cycling. 相似文献
20.
Y.M. Astor M.I. Scranton F. Muller-Karger R. Bohrer J. García 《Marine Chemistry》2005,97(3-4):245-261
Monthly seawater pH and alkalinity measurements were collected between January 1996 and December 2000 at 10°30′N, 64°40′W as part of the CARIACO (CArbon Retention In A Colored Ocean) oceanographic time series. One key objective of CARIACO is to study temporal variability in Total CO2 (TCO2) concentrations and CO2 fugacity (fCO2) at this tropical coastal wind-driven upwelling site. Between 1996 and 2000, the difference between atmospheric and surface ocean CO2 concentrations ranged from about − 64.3 to + 62.3 μatm. Physical and biochemical factors, specifically upwelling, temperature, primary production, and TCO2 concentrations interacted to control temporal variations in fCO2. Air–sea CO2 fluxes were typically depressed (0 to + 10 mmol C m− 2 day− 1) in the first few months of the year during upwelling. Fluxes were higher during June–November (+ 10 to 20 mmol C m− 2 day− 1). Fluxes were generally independent of the slight changes in salinity normally seen at the station, but low positive flux values were seen in the second half of 1999 during a period of anomalously heavy rains and land-derived runoff. During the 5 years of monthly data examined, only two episodes of negative air–sea CO2 flux were observed. These occurred during short but intense upwelling events in March 1997 (−10 mmol C m− 2 day− 1) and March 1998 (− 50 mmol C m− 2 day− 1). Therefore, the Cariaco Basin generally acted as a source of CO2 to the atmosphere in spite of primary productivity in excess of between 300 and 600 g C m− 2 year− 1. 相似文献