Distribution, abundance and life history of Mysis relicta (Lovén) in the Feldberg Lake District, Germany

Distribution, abundance and life history characteristics of Mysis relicta were studied in the Feldberg Lake District (Lake Breiter Luzin, Lake Schmaler Luzin, Lake Zansen) located in northeastern Germany. Between July 2001 and November 2002 mysids were collected by vertical net hauls. In order to determine the impact of the current trophic conditions on the distribution of mysids in these lakes, oxygen concentration, total phosphorus, chlorophyll a and water transparency were also measured. All investigated lakes are mesotrophic at present. Lake Breiter Luzin exhibited great seasonal and spatial variations in mysid abundance. Density of adults and juveniles had a mean of 44.9 ± 57.1 and 68.7 ± 99.6 m⁻², respectively. Highest abundance of adults was 110.4 ± 76.5 m⁻² in summer, lowest abundances of 2.0 ± 4.0 m⁻² occurred in spring. For juveniles, highest density of 218.4 ± 174.6 m⁻² was detected in summer and lowest of 0.8 ± 1.8 m⁻² in winter. No mysids were caught in any of the daytime hauls, but they were widely distributed throughout the water column at night. Size frequency distribution of mysids suggested that reproduction occurred year-round, the most consistent influx of juveniles occurred in early summer and a smaller second cohort in autumn. Highest mysid abundance was 189.2 ± 318.6 adults and 127.0 ± 66.3 juveniles m⁻² in Lake Schmaler Luzin, and 59.6 ± 5.6 adults and 79.4 ± 11.2 juveniles m⁻² in Lake Zansen. There were great spatial differences in abundance in both lakes.     

The role of biogenic structures on the biogeochemical functioning of mangrove constructed wetlands sediments - A mesocosm approach

Benthic metabolism (measured as CO₂ production) and carbon oxidation pathways were evaluated in 4 mangrove mesocosms subjected daily to seawater or 60% sewage in the absence or presence of mangrove trees and biogenic structures (pneumatophores and crab burrows). Total CO₂ emission from darkened sediments devoid of biogenic structures at pristine conditions was comparable during inundation (immersion) and air exposure (emersion), although increased 2-7 times in sewage contaminated mesocosms. Biogenic structures increased low tide carbon gas emissions at contaminated (30%) and particularly pristine conditions (60%). When sewage was loaded into the mesocosms under unvegetated and planted conditions, iron reduction was substituted by sulfate reduction and contribution of aerobic respiration to total metabolism remained above 50%. Our results clearly show impacts of sewage on the partitioning of electron acceptors in mangrove sediment and confirm the importance of biogenic structures for biogeochemical functioning but also on greenhouse gases emission.     

麻江古油藏油源识别与油气运聚分析：来自油气地球化学的证据

充分考虑热演化过程中烃源岩干酪根、族组分、固体沥青及正构烷烃碳同位素相互关系及变化规律,通过地球化学分析并结合前人碳同位素及芳烃标志物研究进行综合分析,结果表明古油藏各区域储层早期均存在下寒武统黑色泥岩来源,后期来源有较大差别,麻江古背斜以南各地沥青均不同程度与中寒武统都柳江组有关,北凯里液态原油及油苗为五峰组及龙马溪组印支期成藏产物,其保存环境为储层早期成岩过程中形成的独立封闭系统。在油源识别的基础上,结合构造地质背景、油气成藏条件及流体活动规律分析,认为黔南坳陷及邻区下寒武统、都柳江组、五峰组及龙马溪组烃源岩的分布控制了该区油气富集规律,黔南海西期断裂系统与加里东运动形成的不整合面构成不同期次油气运聚的输导系统,海西期形成的一系列正断裂是麻江古油藏成藏的关键。     

中国北方岩溶地下水污染分析

近年来,受气候变化和强烈人类活动的影响,环境物质及能量多频次、大范围的输入,极大程度上改变着岩溶水系统的水环境质量,岩溶水生态环境遭受不同程度的威胁和破坏,岩溶水水质日趋恶化。本文归纳分析了我国北方岩溶水系统水质特征、污染现状、污染来源及污染途径。我国北方岩溶水水质类型中硫酸盐型水和氯化物型水的分布逐渐增加,主要污染组分为总硬度、SO42-、F-、NO3-和TDS等。其中硫酸盐和硝酸盐污染强度和范围最大,呈现出显著的人类活动影响特征。依据我国北方岩溶系统结构及水力学特征,将岩溶水污染途径概括为：①连续入渗型——主要包括岩溶区地表水（河流、水库等）渗漏污染,城镇污水渠或排污管道破损引起的污水渗漏污染;②越流型污染——污染孔/裂隙水（含矿坑水/老窑积水等）越流污染岩溶水;③间歇入渗型——固废淋溶入渗和污水灌溉渗漏污染等。据此提出了推进岩溶水水资源保护和污染防治的合理化建议。     

熵值理论和改进BP网络在湖泊富营养化评价中的应用研究

针对湖泊型饮用水源地水体污染、富营养化加剧的问题,引入熵值理论,建立单指标营养状态指数(TSI)和熵权藕合的湖泊综合营养状态指数模型(STSI),计算得到湖泊综合富营养状态指数判断湖泊富营养综合状态;基于神经网络仿真理论和Matlab软件系统,采用附加动量法和自适应学习速率改进BP算法,建立5-3-1结构型式的BP网络模型对湖泊富营养状态进行仿真预测。综合富营养化指数模型及改进BP模型应用于评价及预测固城湖富营养状态,并对模型评价结果进行验证。结果表明,改进BP网络模型可以有效地综合判断水体状态,为富营养评价及预测提供新的方法。     

Foraminifera in Cenozoic Paleoenvironments

INTRODUCTION Microfossilsaregenerallythemostversatileand “useful”offossilsforbothcorrelationandagedeter minationandpaleoenvironmentalanalysis.Among microfossilstheforaminiferaarepre eminent(Fig. 1).Wefindinthesamesample—beitoutcropor subsurface,onshor…     

Carbonates calibrated against oceanographic parameters along a latitudinal transect in the Gulf of California, Mexico

Trophic resources are an important control governing carbonate production. Though this importance has long been recognized, no calibration exists to quantitatively compare biogenic assemblages within trophic resource fields. This study presents a field calibration of carbonate producers in a range of settings against high‐resolution in situ measurements of nutrients, temperature and salinity. With its latitudinal extent from 30° to 23° N, the Gulf of California, Mexico, spans the warm‐temperate realm and encompasses nutrient regimes from oligo‐mesotrophic in the south to eutrophic in the north. Accordingly, from south to north carbonates are characterized by: (i) coral‐dominated shallow carbonate factories (5–20 m water depth) with average sea‐surface temperatures of 25 °C (min. 18 °C, max. 31 °C), average salinities of 35·06‰ and average chlorophyll a levels, which are a proxy for nutrients, of 0·25 mg Chl a m^?3 (max. 0·48, min. 0·1). (ii) Red algal‐dominated subtidal to inner‐shelf carbonate formation (10–25 m) in the central Gulf of California exhibiting average temperatures of 23 °C (min. 18 °C, max. 30 °C), average salinities of 35·25‰, and average Chl a levels of 0·71 Chl a m^?3 (max. 5·62, min. 0). (iii) Molluskan bryozoan‐rich inner to outer shelf factories in the northern Gulf of California (20–50 m) with average sea surface temperatures of only 20 °C (min. 13 °C, max 29 °C), average salinities of 35·01‰, and average contents of 2·2 mg Chl a m^?3 (max. 8·38, min. 0). By calibrating sedimentological data with in situ measured oceanographic information in different environments, the response of carbonate producers to environmental parameters was established and extrapolated to carbonates on a global scale. The results demonstrate the importance of recognizing and quantifying trophic resources as a dominant control determining the biogenic composition and facies character of both modern and fossil carbonates.     

CO<Subscript>2</Subscript> Air–Sea Exchange due to Calcium Carbonate and Organic Matter Storage,and its Implications for the Global Carbon Cycle

Release of CO₂ from surface ocean water owing to precipitation of CaCO₃ and the imbalance between biological production of organic matter and its respiration, and their net removal from surface water to sedimentary storage was studied by means of a quotient θ = (CO₂ flux to the atmosphere)/(CaCO₃ precipitated). θ depends not only on water temperature and atmospheric CO₂ concentration but also on the CaCO₃ and organic carbon masses formed. In CO₂ generation by CaCO₃ precipitation, θ varies from a fraction of 0.44 to 0.79, increasing with decreasing temperature (25 to 5°C), increasing atmospheric CO₂ concentration (195–375 ppmv), and increasing CaCO₃ precipitated mass (up to 45% of the initial DIC concentration in surface water). Primary production and net storage of organic carbon counteracts the CO₂ production by carbonate precipitation and it results in lower CO₂ emissions from the surface layer. When atmospheric CO₂ increases due to the ocean-to-atmosphere flux rather than remaining constant, the amount of CO₂ transferred is a non-linear function of the surface layer thickness because of the back-pressure of the rising atmospheric CO₂. For a surface ocean layer approximated by a 50-m-thick euphotic zone that receives input of inorganic and organic carbon from land, the calculated CO₂ flux to the atmosphere is a function of the CaCO₃ and C_org net storage rates. In general, the carbonate storage rate has been greater than that of organic carbon. The CO₂ flux near the Last Glacial Maximum is 17 to 7×10¹² mol/yr (0.2–0.08 Gt C/yr), reflecting the range of organic carbon storage rates in sediments, and for pre-industrial time it is 38–42×10¹² mol/yr (0.46–0.50 Gt C/yr). Within the imbalanced global carbon cycle, our estimates indicate that prior to anthropogenic emissions of CO₂ to the atmosphere the land organic reservoir was gaining carbon and the surface ocean was losing carbon, calcium, and total alkalinity owing to the CaCO₃ storage and consequent emission of CO₂. These results are in agreement with the conclusions of a number of other investigators. As the CO₂ uptake in mineral weathering is a major flux in the global carbon cycle, the CO₂ weathering pathway that originates in the CO₂ produced by remineralization of soil humus rather than by direct uptake from the atmosphere may reduce the relatively large imbalances of the atmosphere and land organic reservoir at 10²–10⁴-year time scales.