不同发展模式下资源环境承载力评价——以海南省为例

文章关注于产业、人口与资源环境要素的作用关系,建构了资源环境承载力综合评价框架,并以海南省为案例区开展应用研究。该框架首先对区域产业重要性进行评价并分级,为产业结构调整提供依据;其次解析了区域产业、人口资源消耗与污染排放强度,最后,基于产业评价结果设定不同的产业结构调整情景,结合产业和人口的资源消耗与污染排放强度评价不同产业结构下的资源环境承载力,即产业和人口的规模上限。结果表明：2016年海南省的经济规模并未超载,产业有进一步发展空间。其中土地资源成为海南省发展的首要限制因素,其次是水环境;海南经济效益较高的支柱产业和基础性产业多为高耗水、高污染的产业,亟需加强水资源的集约利用,并降低污染排放强度。为提升经济发展规模上限,需要培育低能耗、低排放的产业。文章建构的资源环境承载力评价方法将产业、人口与资源环境相联系,其评价结果政策意义更为明确,可为优化产业结构调整、控制产业及人口发展规模提供决策参考。     

中国北方四条河口的汞——以大辽河、鸭绿江、滦河、东村河为例

分别于1989年，1992年，1991年8月，1991年5月对大辽河口、鸭绿江口、滦河口、东村河口水体中总汞进行了取样和分析，其中又对大辽河口和东村河口进行了溶解态汞的分析。大辽河口和东村河口溶解态汞的含量分别为85～460ng/L和180～500ng/L，平均值分别为210和324ng/L；总汞含量分别为95～550和400～1000ng/L，平均值分别为310和640ng/L。大辽河河流段和河口段溶解态汞和颗粒态汞是主要存在形式。河口溶解态汞和颗粒态汞随氯度变化趋势相似。东村河口溶解态汞约占50%。鸭绿江口和滦河口总汞含量分别为30～2500和3700～6700ng/L，平均值分别为700和5700ng/L。鸭绿江口总汞随氯度变化趋势与随浊度变化趋势一致。而在滦河口总汞含量随两者变化趋势则不同。还讨论了滦河口、东村河口、鸭绿江口和大辽河口汞的污染程度。     

Trace metal composition of colloidal organic material in marine environments

Marine colloidal material (1 kDa–0.2 μm) was isolated by cross-flow ultrafiltration followed by diafiltration and freeze-drying from surface waters of the Gulf of Mexico and the Middle Atlantic Bight (MAB), as well as from estuarine waters of Galveston Bay. Elemental characterization of isolated colloidal material included organic carbon (OC) and selected trace metal (Cu, Pb, Zn, Cd, Co, Ni, Cr, Be, Fe, Al, Mn, V, Ba, and Ti) determinations. It was found that levels of these metals in marine colloids ranged from <0.1 to 50 μg/g colloidal matter, except for Fe which generally had a concentration >120 μg/g. Most metals (Cu, Pb, Zn, Ni, Al, Mn, V, and Ti) had an average concentration >1 μg/g while concentrations of Cd, Co and Be were usually <1 μg/g. Metal concentrations (μg/g) in isolated colloids were, in general, higher in Galveston Bay than in the Gulf of Mexico, suggesting either high abundance of trace metals in estuarine waters or differences in organic matter composition. Higher colloidal metal concentrations in the MAB than in the Gulf of Mexico might be due to higher terrestrial inputs in the MAB. Colloidal metal concentrations (μg/g) were generally lower than those in average soils, continental crust and suspended particles. However, metal/aluminum ratios (Me/Al) in isolated marine colloids were significantly higher than those for average soils and continental crust. Most importantly, colloids had a metal composition and metal/OC ratio (Me/C) similar to humic substances and marine plankton, suggesting that marine colloids largely originate from planktonic sources and are composed of predominately organic components. The Me/C ratios of Galveston Bay colloids followed the sequence of Cu>Ni, Cr, Zn>Mn>Co>Pb, Cd, which is similar to the Irving–Williams order except for Mn, suggesting that the interaction of metals with marine colloids is determined by the affinity of metals for specific organic ligands.     

舟山海域陆源溶解有机质变化及其对近岸羽状流的响应

2007年夏季在东海舟山海域河口锋区开展了陆源溶解有机质的调查研究。测定了有色溶解有机质(CDOM)在激发波长370 nm/发射波长460 nm处的荧光强度和在λ=355 nm处的吸收系数,用于代表陆源CDOM浓度,并测定了荧光指数以指示CDOM来源。结果表明,CDOM的荧光值和紫外吸收系数之间呈显著正相关性,陆源CDOM浓度大体有向海方向降低的趋势,但是纵向上存在一些"突跃"现象。在舟山海域东北角不时观测到表层水体含有高浓度的CDOM,但变异性很大,推测可能该海区受到长江口羽状流的影响。在连续观测站发现陆源CDOM浓度在低平潮时往往比高平潮时要高。河海水在混合过程中CDOM浓度与盐度呈显著的线性负相关关系。在低盐度的悬沙锋区(S<24)CDOM浓度明显低于理论稀释值,而在较高盐度的羽状锋区,CDOM浓度接近于理论稀释值。在盐度为24~31范围内,大部分水样的荧光指数在1.50上下波动,表明其中CDOM来源以陆地来源为主;在较低盐度(S<24)的水样中荧光指数在1.70至1.90以上,表明CDOM以海洋来源为主,这与其陆源组分在高浊度的低盐度区存在显著的去除过程有关。研究表明,舟山海域水质存在着显著的变异性,与近岸羽状流密切相关,陆源溶解有机质的分布特征对此有较好的响应。     

南海溶解氧垂直结构的季节变化分析

溶解氧在生物活动较小的情况下,与温盐相似,同样具有保守性。本文基于WOD05数据集中实际观测的溶解氧标准层资料,对南海溶解氧的垂直结构及其季节变化进行阐述,指出在浅水陆架区、中央海盆和吕宋岛以东深水区,溶解氧具有不同的垂向分布特点。重点分析了深水区的溶解氧垂向结构,发现其极大值存在季节性变化,量值在冬、春较大,夏、秋较小,出现的深度夏季最深,超过50 m,秋、冬较浅且现象不够明显;极小值基本不存在季节变化,出现的深度约860 m;对比温盐关系曲线,发现溶解氧极大值对应着南海次表层水团上界、衰减缓慢的稳定阶段对应次表层水团高盐核心水层、而极小值则对应中、深层水团的交界。     

长江口邻近海域溶解态铝的分布及季节变化

基于2006年6、8、10月对长江口邻近海域的大面调查资料,分析了溶解态Al的分布及季节变化,讨论了水团混合、悬浮颗粒物及浮游植物水华对溶解态铝分布的影响。结果表明,3个航次溶解态铝的水平分布规律相似,都是近岸浓度最高,随着离岸距离的增加浓度降低,6、8、10月溶解态Al的平均浓度分别为(119±77)、(109±80)和(138±73)nmol/L,统计结果表明该海域的溶解态铝具有明显的季节变化。影响溶解态铝分布的主要因素有水团混合、底沉积物的再悬浮以及浮游植物的调节作用。     

北极孔斯峡湾表层沉积物中溶解有机质的来源与转化历史

在北极地区孔斯峡湾采集28个表层沉积物样品,测定了其中水溶性有机质(也称溶解有机质,DOM)的分子量分布、紫外/可见吸收光谱和三维荧光光谱特征,并利用平行因子分析(PARAFAC)模型对DOM的荧光组分和来源进行了解析。结果表明:孔斯峡湾表层沉积物中有色溶解有机质(CDOM)及其中的荧光溶解有机质(FDOM)含量均从内湾向外湾方向呈逐渐累积的趋势,但CDOM中的FDOM所占比例逐渐减小,与DOM趋于老龄化密切相关。沉积作用减弱以及长期的光化学降解和微生物降解作用对此起主要贡献,并导致腐殖质和小分子组分在沉积物DOM中所占的比例呈逐渐递增的趋势。沉积物DOM包含陆源类腐殖质、自生源类腐殖质和类蛋白等三个荧光组分,但是其组成比例空间差异很大。吸收光谱斜率比(S_R)随自生源所占百分比增加而减小,随DOM腐殖质组分中陆源与自生源的比值增加而增加;腐殖化指数(HIX)随类腐殖质与类蛋白质比值和水深的增加而增加,生物源指数(BIX)随自生源比例增加而增加。峡湾沉积物DOM的组成和来源存在着高度的空间差异,在冰川湾区由水体颗粒有机质(POM)的近期转化和迁移而来,而在峡湾中央及口门附近以较老的腐殖质为优势,主要源于水体DOM长期迁移和转化。研究表明,FDOM/CDOM,S_R,HIX和BIX等构成的CDOM光谱指纹信息可以作为揭露沉积物溶解有机质来源及迁移转化历史的工具,对探索海洋与冰川相互作用影响下的峡湾环境演变有着重要意义。     

南海中部和北部上层海水中溶存甲烷浓度及海气交换通量*

根据2010年4—5月国家基金委南海多学科综合航次在南海中部和北部的调查资料,利用抽真空气相色谱法测定海水中溶存甲烷浓度,分析了该海区上层海水中溶存甲烷的浓度、饱和度及海气交换通量。南海中部和北部表层海水中溶存甲烷浓度范围为1.15—5.6nmol·L?1,平均值为2.2nmol·L?1,饱和度范围为59.7%—298.8%,59%站位的溶存甲烷处于过饱和状态。甲烷海气交换通量范围分别为?17.7—61.3μmol·m?2·d?1(根据 LM-86方程计算)和?27.9—119.6μmol·m?2·d?1(根据 W-92方程计算)。南海是大气中甲烷的来源之一,年甲烷辐射量估算值为2.7×10?2—4.0×10?2Tg·a?1。     

环境因子对贝类累积溶解态重金属的影响

对溶解态重金属的吸收是贝类累积重金属的重要来源之一,易受到生物因素和非生物因素的影响。综述溶解氧、温度、空气预暴露、化学物质预暴露等环境因子,诱导的机体代谢过程的改变,对溶解态重金属的累积和转运过程的影响。强调了贝类对溶解态重金属的转运除了被动转运之外,还涉及到需要ATP供能的主动转运过程。     

Characterization of chromophoric dissolved organic matter (CDOM) in the Baltic Sea by excitation emission matrix fluorescence spectroscopy

Chromophoric dissolved organic matter (CDOM) is the major light absorber in the Baltic Sea. In this study, excitation emission matrix (EEM) fluorescence spectra and UV–visible absorption spectra of CDOM are reported as a function of salinity. Samples from different locations and over different seasons were collected during four cruises in 2002 and 2003 in the Baltic Sea in both Pomeranian Bay and the Gulf of Gdansk. Absorption by CDOM decreased with increased distance from the riverine source and reached a relatively stable absorption background in the open sea. Regression analysis showed that fluorescence intensity was linearly related to absorption by CDOM at 375 nm and a_CDOM(375) absorption coefficients were inversely related to salinity. Analysis of CDOM-EEM spectra indicated that a change in composition of CDOM occurred along the salinity gradient in the Baltic Sea. Analysis of percent contribution of respective fluorophore groups to the total intensity of EEM spectra indicated that the fluorescence peaks associated with terrestrial humic components of the CDOM and total integrated fluorescence decreased with decreasing CDOM absorption. In contrast, the protein-like fraction of CDOM decreased to a lesser degree than the others. Analysis of the percent contribution of fluorescence peak intensities to the total fluorescence along the salinity gradient showed that the contribution of protein-like fluorophores increased from 2.6% to 5.1% in the high-salinity region of the transect. Fluorescence and absorption changes observed in the Baltic Sea were similar to those observed in similar transects that have been sampled elsewhere, e.g. in European estuaries, Gulf of Mexico, Mid-Atlantic Bight and the Cape Fear River plume in the South Atlantic Bight, although the changes in the Baltic Sea occurred over a much smaller salinity gradient.