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1.
Accurate and rapid determination of inorganic carbon constituents in ocean environments is important for understanding the carbon cycle, especially in the context of ocean-acidification research. A microsensor capable of directly measuring carbonate ion (CO3 2–) concentrations would be desirable. In this study, a carbonate microsensor with a polymeric liquid membrane was fabricated, and two calibration methods were used to evaluate its performance. The first method was based on continuous titration. Small increments of HCl were added to seawater or Na2CO3 solution to adjust the total alkalinity and pH values and thus obtain a series of carbonate concentrations. The second method used a series of discrete standards. Varying amounts of HCl or NaOH were added to separate seawater aliquots, and the CO3 2– concentration of each standard was calculated from the resulting total alkalinity and total dissolved inorganic carbon. Both methods were found to be adequate for achieving accurate calibration of the CO3 2– sensor, and both are suitable for field work. The discrete standards method, however, is more convenient and may provide a better linear range at low CO3 2– concentrations (detection range: 2–300 μmol/kg) than the continuous titration method in seawater (detection range: 10–250 μmol/kg). This CO3 2– microsensor can be used for 5–7 d and detects changes in carbonate concentration as low as 2 μmol/kg in the inorganic carbon constituents of the environments where marine calcareous organisms grow. The CO3 2– microelectrode was further assessed by applying it to the measurement of pore-water CO3 2– concentration profiles in a marine sediment core. 相似文献
2.
Ocean acidification damages calcareous organisms, such as calcifying algae, foraminifera, corals, and shells. In this study,
we made a device equipped with a Clark-type oxygen electrode and a pH-stat to examine how the most abundant calcifying phytoplankton,
the coccolithophorid Emiliania huxleyi, responded to acidification and alkalization of the seawater medium. When E. huxleyi was incubated at pH 8.2, close to oceanic pH, the medium was alkalized during photosynthesis, and the alkalization rate [determined
as μmol HCl added (mg Chl)−1 h−1] was identical to the activity of photosynthesis [determined as μmol O2 evolved (mg Chl)−1 h−1]. When pH was maintained at 7.2 by the pH-stat, alkalization activity was stimulated and exceeded photosynthetic activity,
resulting in an increase in the ratio of alkalization to photosynthesis (Alk/PS). On the other hand, no alkalization and photosynthesis
were observed at pH 9.2. In contrast, acidification of seawater was observed in the dark because of the release of respiratory
CO2 from cells at pH 8.2–9.2, but not at pH 7.2. When orthophosphate was rapidly depleted within a day in the batch culture,
intracellular calcification gradually increased, and both photosynthesis and alkalization decreased gradually. During the
period the Alk/PS ratio also decreased gradually. These results indicate that E. huxleyi possesses an ability to compensate for the acidification of seawater when photosynthesis is more actively driven than respiration.
These results suggest that the E. huxleyi cells may not be severely damaged by oceanic acidification during photosynthesis because of their homeostatic function to
avoid negative effects on cellular activity. Finally, we concluded that E. huxleyi cells possess a buffering ability to reduce acidification effects when photosynthesis is actively driven. 相似文献
3.
Kenneth S Johnson 《Marine Chemistry》1982,11(3):285-286
Recently, the stoichiometric association constant for MgSO4o in seawater was presented as being inconsistent with thermodynamic data. The results obtained are refuted here as being inaccurate due to assumptions made concerning the activity coefficient of the MgSO4o ion pair. 相似文献
4.
提要以伊红染色法检测样品精子存活率为依据,研究了4℃下5种保存液及Ca2 、Mg2 离子对中华绒螯蟹精子体外保存效果的影响。5种保存液分别为人工海水(ASW)、2倍钙离子人工海水(2×Ca2 -ASW)、无镁离子人工海水(Mg2 -FASW)、无钾离子人工海水(K -FASW)、无钙离子人工海水(Ca2 -FASW),经4天保存后,各保存液中精子样品的存活率和精子密度均出现明显差异,K -FASW、ASW及2×Ca2 -ASW三种保存液中的精子因发生顶体反应而大量死亡,而Mg2 -FASW、Ca2 -FASW的保存效果较好。在此基础上,进一步探讨了不同Mg2 和Ca2 浓度对精子存活率的影响,结果发现,经24h保存后各实验组精子存活率均随着两种离子浓度的增加而明显下降。上述结果表明:K -FASW、ASW及2×Ca2 -ASW不适合精子保存,而Mg2 -FASW和Ca2 -FASW均可作为该蟹精子的保存液;Ca2 因可引起精子顶体反应而造成保存液中精子的大量死亡,其浓度与存活率呈明显的负相关;无K 的保存液中,Ca2 、Mg2 的存在与否对精子的保存效果起关键作用;无Mg2 人工海水之所以具有较好的保存效果,可能与Mg2 的缺乏而导致Ca2 逆浓度差转运受阻,避免了因Ca2 进入而诱发顶体反应有关。 相似文献
5.
The solubility of aluminum hydroxide in seawater of 35‰ salinity at pH = 7.4−8.2 and 25°C was determined experimentally for
three samples synthesized in different ways. The solubilities of two phases subjected to ageing and precipitated (a) from
a boiling solution of aluminum sulfate and (b) immediately from seawater at room temperature were a little different and showed
the minimum within pH = 8.05−8.10. The solubility of aluminum hydroxide precipitated from a solution of sulfate aluminum at
room temperature and not subjected to ageing was about twofold at pH∼7.9. The analysis of the pH dependence of the concentration
of dissolved aluminum allows one to suppose that an Al(OH)2+ hydroxo complex is the primary form of the aluminum occurrence in seawater at pH < 8.05, whereas the Al(OH)4− anion is prevailing at pH > 8.10. Electrically neutral Al(OH)30 hydroxocomplexes may be prevailing within the narrow range of pH = 8.05−8.10 and, in general, are of secondary importance. 相似文献
6.
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
7.
根据2018年7月、11月和2019年1月、4月对广东考洲洋牡蛎养殖海域进行4个季节调查获得的p H、溶解无机碳(DIC)、水温、盐度、溶解氧(DO)及叶绿素a(Chla)等数据,估算该区域表层海水溶解无机碳体系各分量的浓度、初级生产力(PP)、表层海水CO2分压[p(CO2)]和海-气界面CO2交换通量(FCO2),分析牡蛎养殖活动对养殖区碳循环的影响。结果表明:牡蛎养殖区表层海水中Chl a、DIC、HCO3–和PP显著低于非养殖区;养殖淡季表层海水中pH、DO、DIC、HCO3–、和CO32–显著大于养殖旺季,养殖旺季的p(CO2)和FCO2显著大于养殖淡季。牡蛎养殖区表层海水夏季、秋季、冬季和春季的海-气界面CO2交换通量FCO2平均值分别是(42.04±9.56)、(276... 相似文献
8.
9.
采用化学沉淀法成功制备了Cu2+/SnO2复合纳米光催化剂,采用XRD、SEM等测试手段对复合纳米光催化剂的粒径、形态等进行表征。在紫外光条件下,分别改变催化剂掺杂比、催化剂煅烧温度、催化剂投加量、柴油初始含量和光照时间等单因素,探究不同条件对Cu2+/SnO2复合纳米光催化剂降解海洋柴油污染物的影响。结果表明,自制复合纳米光催化剂可以有效降解海水中的柴油污染物,在紫外光作用下,于400℃下煅烧Cu/Sn掺杂比为0. 03的Cu2+/SnO2复合纳米光催化剂、投加量为0. 2 g/dm3、柴油初始含量为0. 15 g/dm3、H2O2溶液含量为0. 2 g/dm3、溶液的p H为7、光照时间3 h时效果最好,海水中柴油的去除率最高,达到86. 98%。Cu2+/SnO2复合纳米光催化剂用聚丙烯纳米球负载后可以实际应用于海洋中,便于回收。 相似文献
10.
A theoretical evaluation of basic thermodynamic relationships reveals that variation of activity coefficients, ion pairing and electrical interactions must be considered when modelling ionic diffusion in seawater. The contributions of ion-pair formation and change in activity coefficient along the diffusion path were studied experimentally by conducting diffusion experiments in which solutions of KCl, NaCl, MgCl2, Li2SO4, K2SO4, Na2SO4 and MgSO4, at an ionic strength of 0.7, were allowed to diffuse into distilled water. The study reveals that the thermodynamic factor, required to correct for changes in the activity coefficient along the diffusion path, is significant for all the salts studied. Agreement between a simple diffusion model, which does not include ion pairing, and observed data was good for completely dissociated salts, but poor for salts which are known to form ion pairs at the concentration levels studied. The diffusion of MgSO4, 0.425 of which is associated at I = 0.7, was successfully modelled by assuming that the diffusion coefficient of the MgSO40 ion pair is different from the diffusion coefficient of the dissociated salt. The diffusion coefficient of this ion pair is estimated to be 1.9 × 10−5 cm2 s−1 at 30°C, as compared to 0.49 × 10−5 cm2 s−1 for the dissociated salt. It is suggested that the high mobility of this ion pair could cause magnesium enrichment in pore water of sulfate depleted sediments. 相似文献
11.
海洋中的氮循环是海洋生物地球化学研究的热点领域之一,而硝化过程是氮循环的关键一环,准确获取硝化速率对于丰富海洋氮循环的认识至关重要。15N标记同位素技术是目前国际上最为广泛使用的硝化速率测定方法,该方法的核心在于准确测定15N加富样品产生的15NO2-和15NO3-的含量,但目前的方法普遍存在测试时间较长、测试成本较高、所需样品体积较大或者检测限较高等问题。研究以低成本的膜进样质谱作为15N加富样品测试设备,建立了基于镉柱与氨基磺酸双还原体系测定15N加富样品中15NO3-含量的方法。经条件优化实验确定的具体方法:采用1 mol/L HCl配制15 mmol/L的氨基磺酸（SA）作为反应试剂除去样品原有的NO2-,然后利用镉柱将15NO 相似文献
12.
ZHANG Naixing SONG Jinming CAO Conghu REN Rongzhu WU Fengcong ZHANG Shaoping SUN Xu 《海洋学报(英文版)》2012,31(1):73-82
The influence of macronitrogen (NO - 3 and NH + 4 ) addition with Ulva pertusa on dissolved inorganic carbon system in seawater was studied. The results indicate that p(CO 2 ) and HCO 3 concentration decrease significantly, while pH and CO 2- 3 concentration increase significantly. When the concentration of NO 3 was less than 71 μmol/dm 3 or NH + 4 was less than 49.7 μmol/dm 3 , dissolved inorganic carbon (DIC) absorption rates by Ulva pertusa generally increased with the increasing of nitrogen concentration. The DIC decreased 151 μmol/dm 3 with the addition of 71 μmol/dm 3 NO 3 and decreased 232 μmol/dm 3 with the addition of 49.7 μmol/dm 3 NH + 4 after the experiment compared with DIC measured without nitrogen addition. A significant negative-correlation was found between c(DIC) and growth rate (μ) of Ulva pertusa (r = -0.91, P <0.000 1, n=11). NH + 4 had more influence on the species of inorganic carbon system than NO 3 . 相似文献
13.
The protonization constant of HS? (K12) has been determined potentiometrically (glass electrode) at atmospheric pressure in synthetic seawater in the salinity range 2.5–40‰ at 5 and 25°C and in NaCl solutions in the formal ionic strength of 0.1–0.8 M at 5 and 25°C. The difference between synthetic seawater and an NaCl solution with the same formal ionic strength can be explained in terms of the complexation of H+ by sulphate in seawater. These results can be used to compare the pH scales suggested by Hansson (1973c) and Bates (1975). Furthermore, comparison between the present values of K12 and those of Goldhaber and Kaplan (1975) makes it possible to compare the conventional pH scale with Hansson's titration pH scale. The conditional protonization constant of HS? in seawater of different salinities can be used to modify the Gran plots (Hansson and Jagner, 1973) for alkalinity measurements in anoxic seawater. Ion-pair formation between HS? and Mg2+ or Ca2+ seems to be very weak. 相似文献
14.
Concentration and stable isotopic compositions (δ
18O) of dissolved O2 were measured in seawater samples collected from the Philippine Sea in June 2006. The in-situ O2 consumption rate and the isotopic fractionation factor (α
r
) during dissolved O2 consumption were obtained from field observations by applying a vertical one-dimensional advection diffusion model to the
deep water mass of about 1000–4000 m. The average O2 consumption rate and α
r
were, respectively, 0.11 ± 0.07 μmol kg−1yr−1 and 0.990 ± 0.001. These estimated values agree well with values from earlier estimations of Pacific deep water. The in-situ O2 consumption rates are two or more times higher north of 20°N, although the value of α
r
was not significantly different between the north and south. Its levels varied rapidly in the water mass of less about 2000
m depth. These results suggest that organic matter from the continent imparts a meaningful contribution to the upper water
in the northern part of the area; it might produce the strong O2 minimum that is evident in the water mass from about 1000–2000 m in the northern part of the Philippine Sea. 相似文献
15.
Franck Lartaud Laurent Emmanuel Marc de Rafelis Stephane Pouvreau Maurice Renard 《Geo-Marine Letters》2010,30(1):23-34
Compared to oxygen isotopes, the carbon isotope composition of biogenic carbonates is less commonly used as proxy for palaeoenvironmental
reconstructions because shell δ13C is derived from both dissolved inorganic (seawater) and organic carbon sources (food), and interactions between these two
pools make it difficult to unambiguously identify any independent effect of either. The main purpose of this study was to
demonstrate any direct impact of variable food supply on bivalve shell δ13C signatures, using low/high rations of a 13C-light mixed algal diet fed to 14-month-old (adult) cultured Japanese Crassostrea gigas under otherwise essentially identical in vitro conditions during 3 summer months (May, June and July 2003, seawater temperature
means at 16, 18 and 20 °C respectively) in experimental tanks at the Argenton laboratory along the Brittany Atlantic coast
of France. At a daily ration of 12% (versus 4%) oyster dry weight, the newly grown part of the shells (hinge region) showed
significantly lower δ13C values, by 3.5‰ (high ration: mean of −5.8 ± 1.1‰, n = 10; low ration: mean of −2.3 ± 0.7‰, n = 6; ANOVA Scheffe’s test, p < 0.0001). This can be explained by an enhanced metabolic activity at higher food supply, raising 13C-depleted respiratory CO2 in the extrapallial cavity. Based on these δ13C values and data extracted from the literature, and assuming no carbon isotope fractionation between food and shell, the
proportion of shell metabolic carbon would be 26 ± 7 and 5 ± 5% for the high- and low-ration C. gigas shells respectively; with carbon isotope fractionation (arguably more realistic), the corresponding values would be 69 ± 14
and 24 ± 9%. Both groups of cultured shells exhibited lower δ13C values than did wild oysters from Marennes-Ol éron Bay in the study region, which is not inconsistent with an independent
influence of diet type. Although there was no significant difference between the two food regimes in terms of δ18O shell values (means of 0.1 ± 0.3 and 0.4 ± 0.2‰ at high and low rations respectively, non-significant Scheffe’s test),
a positive δ13C vs. δ18O relationship recorded at high rations supports the interpretation of a progressive temperature-mediated rise in metabolic
activity fuelled by higher food supply (in this case reflecting increased energy investment in reproduction), in terms not
only of δ13C (metabolic signal) but also of δ18O (seawater temperature signal). Overall, whole-shell δ18O trends faithfully recorded summer/winter variations in seawater temperature experienced by the 17-month-old cultured oysters. 相似文献
16.
采用3H-TdR同位素示踪方法研究了环境因子对溶藻弧菌对大黄鱼表皮粘液粘附作用的影响。试验结果表明,溶藻弧菌能很好地粘附于大黄鱼表皮粘液,其粘附量在菌浓度不超过6.52×108cfu/ml情况下随菌浓度的升高而升高;粘附量在25℃下孵育180min趋于饱和,在180min以内与孵育时间呈正相关关系;粘附作用在温度25—30℃、pH值偏酸、盐度35条件下较强;在无Na (盐度为0)时,无粘附作用;Ca2 能显著加强溶藻弧菌的粘附作用,而Mg2 作用不明显。这些结果表明,溶藻弧菌对大黄鱼表皮粘液有较强的粘附作用,其粘附作用受温度、盐度、pH值等环境因子的影响。 相似文献
17.
氯离子和硫酸根离子是海水中重要的无机阴离子,在研究海洋生态变化、海洋循环作用过程与海洋全球气候变化等领域具有重要的指示意义。其测定方法较多,但缺少相应的测试方法。本文对测定海水中Cl-,SO42-的离子色谱方法进行了优化,选用IonPacAS14碳酸盐选择性离子色谱柱,以3.5 mmol/L Na2CO3+1 mmol/L NaHCO3为流动相,可消除海水样品中碳酸盐及其他阴离子的干扰。该方法对Cl-检出限为0.29 mg/L,线性相关系数r2=0.999 2,对SO42-检出限为0.42 mg/L,线性相关系数r2=0.997 9。样品的加标回收率在95%~102%,Cl-和SO42-的相对标准偏差分别为1.92%和4.18%。该方法简便、迅速、灵敏、准确度高,可满足批量海水样品中Cl-与SO42-的准确测试。 相似文献
18.
M. Lutfi Firdaus Kazuhiro Norisuye Yusuke Nakagawa Seiji Nakatsuka Yoshiki Sohrin 《Journal of Oceanography》2008,64(2):247-257
Dissolved and labile particulate Zr, Hf, Nb, Ta, Mo and W were determined at stations K1 (51°N, 165°E), K2 (47°N, 160°E),
KNOT (44°N, 155°E) and 35N (35°N, 160°E) in the western North Pacific Ocean. A portion of seawater for dissolved species (D)
was passed through a 0.2 μm Nuclepore filter and acidified to pH 2.2 with HCl and HF. A portion of seawater for acid-dissolvable species (AD) was acidified
without filtration. Labile particulate (LP) species is defined as AD minus D, which represents a chemically labile fraction
of particulate species. D-Zr, Hf and Ta increase with depth, Nb shows a slight depletion in surface water, whereas Mo and
W have a conservative vertical profile. The concentration range of D-Zr, Hf, Nb, Ta and W is 31–275, 0.14–0.95, 4.0–7.2, 0.08–0.29
and 40–51 pmol kg−1, respectively, whereas that of Mo is 97–105 nmol kg−1. LP-species of Zr, Hf and Ta account for 10–14% of AD in average and increase up to 25% below 4000 m, whereas those for Mo
and W are negligible. In contrast, LP-Nb shows maxima (up to 27%) in surface water. We also found that D-Zr/Hf, Nb/Ta and
Mo/W mole ratios generally increase in the order continental crust < river water < coastal sea < open ocean. 相似文献
19.
Association constants of orthophosphate ion with Na+, Ca2+, and Mg2+ were measured at μ = 0.68 and 20°C. The results were used to calculate phosphate speciation in seawater. Free HPO42? ion and MgHPO4o are found to be the predominant species. 相似文献
20.
为了解盐度渐变对黄条鰤(Seriola aureovittata)渗透调节的影响,设置自然海水(对照组盐度为29),5,10,15,20,35六个盐度梯度,并对不同盐度下幼鱼鳃丝Na~+/K~+-ATP酶活力、离子浓度、渗透压进行了检测和分析。结果显示:在盐度5～35,黄条鰤尿、血清、血浆的渗透压均随盐度升高而升高,盐度为35时渗透压均为最高,其中尿的渗透压显著高于血清和血浆渗透压。在盐度从29下降的过程中,鳃丝Na~+/K~+-ATP酶活力、离子浓度、渗透压呈现相似的变化规律,都随着盐度的降低而呈现总体下降的趋势;盐度从29升高到35时,各检测指标中仅有尿和血浆的K~+含量无显著变化(P0.05),其余均显著升高(P0.05)。实验结果表明,黄条鰤生存和繁衍的自然海水盐度29是幼鱼存活的适宜盐度,在略低的盐度20～29均能较快适应,说明在盐度渐变过程中,黄条鰤幼鱼对外界盐度变化有较强的调节能力。 相似文献