NOAA gulf of Mexico status and trends program: Trace organic contaminant distribution in sediments and oysters

Polynuclear aromatic hydrocarbons (PAH), chlorinated pesticides, and polychlorinated biphenyls (PCB) concentrations were determined in sediment and oysters to provide information on the current status of the concentration of these contaminants in Gulf of Mexico coastal areas removed from point sources of input. Coprostanol analyses of sediments showed that anthropogenic materials are associated with the sediments at all 153 stations sampled. The levels of contaminants encountered are low compared with areas of known contamination. Average PAH concentrations are nearly the same in oysters and sediments, although the molecular weight distribution is different. Average DDT and PCB concentrations are higher by a factor of 10 to 130 in oysters as compared to sediments. Continued sampling and analyses will allow for long-term trends in the concentrations of these contaminants to be determined.     

Trace contaminant concentrations in the Kara Sea and its adjacent rivers, Russia.

Trace organic (chlorinated pesticides, PCBs, PAHs and dioxins/furans) and trace metal concentrations were measured in surficial sediment and biological tissues (i.e., worms, crustaceans, bivalve molluscs, and fish livers) collected from the Russian Arctic. Total DDT, chlordane, PCB and PAH concentrations ranged from ND to 1.2, ND to <0.1, ND to 1.5 and <20-810 ng g(-1), respectively, in a suite of 40 surficial sediment samples from the Kara Sea and the adjacent Ob and Yenisey Rivers. High sedimentary concentrations of contaminants were found in the lower part of the Yenisey River below the salt wedge. Total dioxins/furans were analysed in a subset of 20 sediment samples and ranged from 1.4 to 410 pg g(-1). The highest trace organic contaminant concentrations were found in organisms, particularly fish livers. Concentrations as high as 89 ng g(-1) chlordane; 1010 ng g(-1) total DDTs; 460 ng g(-1) total PCBs; and 1110 ng g(-1) total PAH, were detected. A subset of 11 tissue samples was analysed for dioxins and furans with total concentrations ranging from 12 to 61 pg g(-1). Concentrations of many trace organic and metal contaminants in the Kara Sea appear to originate from riverine sources and atmospheric transport from more temperate areas. Most organic contaminant concentrations in sediments were low; however, contaminants are being concentrated in organisms and may pose a health hazard for inhabitants of coastal villages.     

Levels of chlorinated hydrocarbons and trace metals in bivalves and nearshore sediments from the Dominican Republic

Bivalves (Crassostrea rizhophorae, Isognomon alatus, Codakia orbicularis Linné, and Tellina fausta) and sediment samples collected from 12 locations along the Dominican Republic coastline were used to assess the degree of nearshore contamination by selected chlorinated hydrocarbons and heavy metals. Concentrations of total chlordanes, DDTs and PCBs ranged from 0.51 to 7.47 ng/g, < MDL to 30.9 ng/g and 11.3 to 82.3 ng/g, and from < MDL to 1.73 ng/g, 0.21 to 12.5 ng/g and 0.46 to 41.9 ng/g in bivalves and surface sediments, respectively. The concentration ranges of predominantly anthropogenic Cu, Pb and Zn were 3.08–866 μg/g, 0.08–1.46 μg/g and 22.9–4380 μg/g in bivalve soft parts and 1.01–111 mg/g, 0.420–134 μg/g and 1.96–277 μg/g in surface sediments, respectively. Mercury concentrations ranged from 0.290 to 7.02 μg/g and from 0.096 to 0.565 μg/g in both matrices. The relatively high Hg concentrations found in bivalves from two stations in Bahia Samana, near to a known source of past Hg contamination in the sediments, require a more in-depth survey of the area. In general the concentrations of selected chlorinated hydrocarbons and trace metals, compared with those reported for the same matrices in the Caribbean and west Atlantic coastal areas, show at present the existence of only very localized contamination problems in the Dominican Republic.     

华北克拉通南缘中条山-嵩山地区1.78Ga基性岩墙群的地球化学特征及构造环境

幔源岩浆侵位产生的基性岩墙群是地壳伸展裂解的重要标志。华北克拉通南缘中条山-嵩山地区出露有大量的中元古代基性岩墙群,对其研究将有助于深入了解华北克拉通中元古代构造演化特征。其岩石类型以辉绿岩为主,少量辉长辉绿岩和辉绿玢岩;主要造岩矿物为斜长石和单斜辉石,其它矿物包括角闪石、Fe-Ti氧化物、磷灰石、黑云母、碱性长石和石英。锆石SHRIMPU-Pb年龄为1785±18Ma,代表岩墙的结晶年龄。岩石K2O+Na2O含量为3.63%～6.18%,K2O/Na2O比值为0.73～1.38,FeOT含量较高(10.03%～13.59%),属于拉斑玄武岩系列。岩石的稀土元素含量高(142×10-6～381×10-6),亏损Nb、Ta、Zr、Hf等高场强元素,富集Rb、Ba、La等大离子亲石元素,全岩εNd(t)值为-6.2～-8.1。岩墙的固结指数(SI)和MgO含量呈明显的正相关关系,说明幔源岩浆发生过明显的结晶分异作用。地球化学分析表明,研究区基性岩墙属于板内拉斑玄武岩系列,与熊耳群火山岩有相似的地球化学特征;基于两者紧密的产出关系,我们认为该区岩墙可能是熊耳群火山岩的通道岩墙,共同代表了华北克拉通东、西陆块碰撞后伸展事件。     

Chlorinated hydrocarbons in the seawater and surface sediments of Blanca Bay,Argentina

In order to characterize our study area and to provide reference values to be used in the future to measure the changes produced by an increase in contamination, the concentrations of chlorinated hydrocarbons have been investigated in fifty-one samples of seawater, taken at four different depths: air-sea interface, surface, one metre and bottom waters, and in twenty-three samples of surface sediments from Blanca Bay, Argentina. Of eleven organochlorine compounds we were looking for (α BHC, lindane, heptachlor, δ BHC. aldrin, heptachlor epoxide, dieldrin, o-p′DDD, p-p′DDD, o-p′DDT and p-p′DDT), seven could be detected in seawater and three in surface sediments with the following mean concentrations: α-BHC=48·2 ng l^?1; lindane=54·2 ng l^?1; heptachlor=45·0 ng l^?1; δ BHC=12·5 ng l^?1; aldrin=61·8 ng l^?1 and ΣDDT=67·0 ng l^?1; and δ BHC=3·2 ng g^?1; lindane=4·2 ng g^?1 and heptachlor=1·0 ng g^?1 for seawater, regarding the surface waters, and sediment samples, respectively.Concentration factors among the different water layers were also studied to see if there was any correlation between chlorinated hydrocarbon contents and the water depths from which the samples were taken. As a mean value, the air-sea interface water contains 18 times more of these compounds than that of the water near the bottom. A comparison of the values corresponding to seawater and surface sediments from our study area with those levels measured in samples from other geographic locations is also presented.With the purpose to detect a relationship between chlorinated hydrocarbon concentrations and the contents of particulate matter (PM) on the one hand, and particulate organic material (POM) on the other hand, four groups of samples containing different amounts of PM and POM, respectively were formed. From a comparison of the results obtained, lindane, heptachlor and δ BHC showed a tendency to lower concentrations in those samples containing little PM whereas α BHC and aldrin remained without important changes. No significant correlation was found between organochlorine levels and contents of POM.     

铜陵狮子山地区中酸性侵入岩锆石SHRIMP U-Pb定年及岩浆作用的深部过程

铜陵狮子山地区中酸性侵入岩锆石SHRIMP U-Pb定年结果表明,白茫山辉石二长闪长岩、鸡冠山和大团山石英二长闪长岩以及胡村花岗闪长岩的年龄分别为:138.21 ±0.82Ma、139.9 ±1.1Ma、139.3 ±1.2Ma和140.9 ±1.2Ma.岩浆侵位顺序为花岗闪长岩→石英二长闪长岩→辉石二长闪长岩.根据锆石SHRIMP U-Pb年龄变化范围,推测该区岩浆活动持续的时间约为15Ma,且岩浆属脉动式多次侵位,后期岩浆侵位的热使早期岩体中已结晶的锆石发生熔解、重结晶,形成新的锆石.地下深部岩浆活动频繁,形成了多级岩浆房,使得本区的莫霍面界线不明显.     

Stable isotope analysis of consumer food webs indicates ecosystem recovery following prolonged drought in a subtropical estuarine lake

Assessing changes in food-web structure provides a useful monitoring tool for gauging the resilience of ecosystems in the face of climatic impacts. We consider the ecological resilience of a large estuarine lake (St Lucia Estuary, South Africa) in the wake of an extreme climatic event (prolonged drought). Using carbon and nitrogen stable isotopes, food-web structure was assessed at five sites across the estuary during the winter and spring of 2013. Sampling occurred approximately three years after heavy rains flooded the system and returned it to a relatively diluted state following an almost decade-long drought that decimated food webs in the upper parts of the estuary due to hypersalinity effects. Comparisons of niche width and variance of consumer food webs among sites revealed a general homogenisation of food webs across the entire system, contrasting with the spatial differentiation of food webs documented during the drought phase. Our results indicate that the estuary is able to maintain ecological resilience at the whole-system level in the face of an extreme drought. This is likely facilitated by source pools of species residing in the relatively stable lower estuary, which are able to rapidly recolonise areas denuded by drought in the upper estuary.     

Galveston Bay: Temporal changes in the concentrations of trace organic contaminants in national status and trends oysters (1986–1994)

The temporal distributions for six classes of trace organic contaminants (chlordanes, DDTs, dieldrin, PAHs, PCBs, and butyltins) in oysters from six Galveston Bay sites from National Oceanic and Atmospheric Administration’s National Status and Trends (NS&T) Mussel Watch Program are compared with other NS&T sites from the Gulf of Mexico as well as all NS&T sites of the United States (East Coast, West Coast, and Gulf of Mexico). Decreases in the median for the Gulf-wide concentration of chlordanes, dieldrin, and butyltins occurred during 1986–1994. The Gulfwide median concentrations of DDTs, PAHs, and PCBs exhibited a strong cyclic distribution with time. For Galveston Bay oysters, “high” concentration is defined as the concentration greater than the median plus one standard deviation for all Gulf of Mexico sites. The percentage of sites having high concentrations during 1986–1994 for Galveston Bay oysters are 49% for dieldrin, 45% for butyltins, 40% for chlordanes, 38% for PCBs, 30% for PAHs, and 21% for DDTs. For PCBs, 43% of Galveston Bay oyster samples analyzed over the first 9 yr have concentrations high enough for potential biological effects to be observed in oysters. The percentages in other agents were chlordanes (22%), butyltins (22%), dieldrin (5%), and PAHs (4%). National Academy of Science-proposed regulatory limits for oysters were exceeded in only 2% of Galveston Bay samples for DDTs and 1% for PCBs. All other contaminants were below proposed NAS limits.