Zinc-rich Pyrite from the TAG Active Mound, the TAG Hydrotherma Field, Mid-Atlantic Ridge

Abstract: Pyrite rich in Zn, up to 3.1 wt%, was found in the TAG active mound of the TAG hydrothermal field, the slow-spreading Mid-Atlantic Ridge at 26°08'N and 44°49'W. The Zn-rich pyrite is characterized by an optical homogeneity, a homogeneous distribution of Zn in the back-scattered electron images, both at a magnification of about 500, a negative correlation between Fe and Zn contents of the pyrite and a rather small unit cell edge (a₀ = 5.4117 ± 0.0008Å), strongly indicating that the detected Zn is present in the pyrite in solid solution. Such Zn concentrations are observed exclusively in dendritic pyrite, suggesting that the Znrich pyrite grew from hydrothermal fluids of a high degree of supersaturation due to quenching on the seafloor.     

针对IPCC评估报告中海洋碳循环的疑问——δ13C收支平衡法的验证

 通过对比IPCC历次评估报告中全球碳循环的收支发现,尽管评估报告在估算各主要碳库及其间的通量时差别不大,但表层至中深层海水间溶解无机碳通量却存在巨大差异。利用δ¹³C的收支平衡检验了这一通量的适用范围,结果表明：IPCC 1996年和2007年评估报告对此通量估计过大,而1990年和2001年评估报告估计偏小。     

Effects of fluid displacement pattern on complex electrical impedance in Berea sandstone over frequency range 104–106 Hz

To better understand the effect of fluid distribution on the electric response of rocks saturated with oil and brine, we conducted experimental studies on the complex electrical impedance in a Berea sandstone, together with in situ acquisitions of oil distribution images employing a high‐resolution medical X‐ray computed tomography. We performed two tests of brine displacement by oil under high (10 MPa) and low (5 MPa) pressures, which were accompanied by fingering and stable displacement patterns, respectively. The measured complex impedance data were fitted to the Cole model to obtain the resistance, capacitance, peak frequency of the imaginary impedance, and the exponent α of the rock–fluid system. With increasing oil saturation, the resistance showed an increasing trend, whereas the other three parameters decreased. The fingering displacement exhibited lower resistance and capacitance than the stable displacement. The analysis of the resistance changes using a simple parallel connection model indicates that there are more components of residual brine in parallel connections in the fingering pattern than in the stable displacement pattern at the same saturation. We also interpreted the normalised changes in the capacitance (or apparent dielectric constant) with respect to the oil saturation via an analysis of the shape factor of fluid distribution based on the Maxwell–Wagner–Brugermann–Hanai model. The changes in the shape factor suggest that the pinch‐off of the brine in parallel connection by the oil is a dominant mechanism reducing the capacitance. In the stable displacement, most of the connections in the brine phase are immediately pinched off by oil displacement front at a local oil saturation of 65%. Conversely, in the fingering displacement, there is a transition from the bulk or layered brine to the pinched‐off at a local oil saturation below 60%. The analyses indicate that the difference in the fluid distribution under different fluid conditions is responsible for the non‐Archie behaviour.     

Contamination and impacts of new antifouling biocide Irgarol-1051 on subtropical coral reef waters

Coral reefs are deteriorating worldwide due to various stresses, including pollution of hazardous chemicals such as antifouling chemicals. Occurrence and impacts of a new antifouling biocide Irgarol-1051 (2-methylthio-4-tert- butylamino -6-cyclopropylamino -s-triazine) have been studied in coral reef waters around Okinawa Islands, Japan. The average concentration of Irgarol detected at commercial and fisheries Ports was 24.70 ± 9.88 ng/L. In Naha Bay, the average concentration of Irgarol was 10.00±12.98 ng/L. The average level detected around the Ports has already approaches the environmental risk limit for the marine organisms. Irgarol was detected in waters at the frequency of 92.3 % (24/26) of the total samples collected during two sampling campaigns (September and December, 2007) at the Ports. In Naha Bay, Irgarol was detected by 40.5 % (17/42) of the total water samples collected monthly from Sep., 2007 to Feb., 2008, indicating that Irgarol is widely detected along the coastal shorelines of Okinawa Island. The eco- toxicological study revealed that the rate of photosynthesis in the coral Galaxea fascicularis was significantly reduced by 18 % and 121 % relative to control when the corals were exposed to 1000 and 10,000 ng/L of Irgarol, respectively. The calcification rate dropped by 98.3 % relative to control when the corals were exposed to 10,000 ng/L of Irgarol. The results of the present study report the wide occurrence of new antifouling biocide Irgarol around coastal areas of Okinawa Island. However, the contamination does not pose serious threat on the photosynthesis and calcification of corals under short term exposure (96 h).     

Simultaneous Measurement of Hydrogen Peroxide and Fe Species (Fe(II) and Fe<Subscript>(tot)</Subscript>) in Okinawa Island Seawater: Impacts of Red Soil Pollution

The northern part of Okinawa Island suffers from red soil pollution—runoff of red soil into coastal seawater—which damages coastal ecosystems and scenery. To elucidate the impacts of red soil pollution on the oxidizing power of seawater, hydrogen peroxide (HOOH) and iron species including Fe(II) and total iron (Fe_(tot), defined as the sum of Fe(II) and Fe(III)) were measured simultaneously in seawater from Taira Bay (red-soil-polluted sea) and Sesoko Island (unpolluted sea), off the northern part of Okinawa Island, Japan. We performed simultaneous measurements of HOOH and Fe(II) because the reaction between HOOH and Fe(II) forms hydroxyl radical (•OH), the most potent environmental oxidant. Gas-phase HOOH concentrations were also measured to better understand the sources of HOOH in seawater. Both HOOH and Fe(II) in seawater showed a clear diurnal variation, i.e. higher in the daytime and lower at night, while Fe_(tot) concentrations were relatively constant throughout the sampling period. Fe(II) and Fe_(tot) concentrations were approximately 58% and 19% higher in red-soil-polluted seawater than in unpolluted seawater. Gas-phase HOOH and seawater HOOH concentrations were comparable at both sampling sites, ranging from 1.4 to 5.4 ppbv in air and 30 to 160 nM in seawater. Since Fe(II) concentrations were higher in red-soil-polluted seawater while concentrations of HOOH were similar, •OH would form faster in red-soil-polluted seawater than in unpolluted seawater. Since the major scavenger of •OH, Br⁻, is expected to have similar concentrations at both sites, red-soil-polluted seawater is expected to have higher steady-state •OH concentrations.     

针对IPCC评估报告中海洋碳循环的疑问——δ13C收支平衡法的验证

通过对比IPCC历次评估报告中全球碳循环的收支发现,尽管评估报告在估算各主要碳库及其间的通量时差别不大,但表层至中深层海水间溶解无机碳通量却存在巨大差异。利用δ¹³C的收支平衡检验了这一通量的适用范围,结果表明：IPCC 1996年和2007年评估报告对此通量估计过大,而1990年和2001年评估报告估计偏小。     

中国南麂列岛产海洋底栖硅藻新种-南麂侧链藻(Pleurosira nanjiensis sp. nov.)的形态与分子系统学研究

本文描述了采自南麂列岛小柴屿岩相潮间带的一海洋底栖硅藻新种,南麂侧链藻（Pleurosira nanjiensis sp.nov.）。本研究使用光学显微镜和扫描电子显微镜对该种进行了形态学观察,并基于SSU rRNA和rbcL基因重建了其系统发育关系。南麂侧链藻具有壳面橄榄形、椭圆形或圆形,壳面隆起,单眼突出于壳表面,2–3个唇状突（rimportulae）,放射排列的线纹等特征,区别于其他侧链藻。     

Occurrence of tributyltin compounds and characteristics of heavy metals

Surface sediment samples were collected from Tanzanian major commercial ports and studied for the distribution and behavior of tributyltin (TBT) compounds and heavy metals. The content of TBT in sediments ranged from ND-3670 ng (Sn) g¹dry wt (1780 ± 1720) (Mean ± SD) at Zanzibar and from ND-16700 ng (Sn)g¹ dry wt (4080 ± 7540) at Dar es Salaam ports, respectively. Maximum TBT levels were detected inside the both ports. Metabolic degradation of butyltin compounds (BTCs) showed that MBT + DBT > TBT %, this may be attributed by the warm ambient water and intense sunlight in the tropical regions. A sequential extraction procedure was undertaken to provide detailed chemical characteristics of heavy metals in the sediments. The procedure revealed that about 50% of Fe in the both ports is in immobile fraction (residual fraction) while other metals; Cd, Cu, Ni, Co, Zn, Pb, and Mn were mostly found in exchangeable or carbonate fractions and thus can be easily remobilized and enter the aquatic food chain. This paper provides basic information of TBT compounds contamination and chemical characteristics of heavy metals in the marine ecosystem in Tanzania. To our knowledge, this is the first documentation of Organotin compounds (OTCs) in marine environments in East Africa and suggests the importance of further detailed OTCs studies in other sub-Saharan Africa regions     

Distribution coefficient of Mg ions between calcite and solution at 10–50°C

The distribution coefficient (λ_Mg) 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 λ_Mg for calcite is small, where the molar ratio lies in the range 0.04-2. However, the λ_Mg 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.     

The coprecipitation of uranium with calcium carbonate

This report is one of the studies on the factors controlling the trace element contents of marine calcareous skeletons. The values of the distribution coefficients of UO₂ ²⁺ between solutions and carbonate precipitates were measured in the laboratory at 20±1C. From the determination of the uranium contents of marine calcareous skeletons and sea water, the values of uranium between marine calcareous skeletons and sea water are expected as 1.2 to 0.3 for aragonite and 0.2 to 0,0n for calcite. The experimentally measured value of the distribution coefficient for aragonite is thermodynamically discussed. And it was known that the value of the distribution coefficient of UO₂ ²⁺ is controlled greatly by the activity coefficient of uranium dissolved in a parent medium and the crystal form of CaCO₃. The activity coefficient of uranium in solution mainly owes to the formation of complexes between UO₂ ²⁺ and CO₃ ^2–in the solution.