Long-Term Temperature Trends and Tree Growth in the Taymir Region of Northern Siberia

The northernmost conifers in the world are located well above the Arctic Circle in the Taymir region of northern Siberia and have been recording the thermal environment for centuries to millennia. The trees respond to temperatures beyond the narrow season of actual cambial cell division by means of root growth, photosynthesis, lignification of cell walls, and other biochemical processes. Data from annual tree-ring widths are used to reconstruct May–September mean temperatures for the past four centuries. These warm-season temperatures correlate with annual temperatures and indicate unusual warming in the 20th century. However, there is a loss of thermal response in ring widths since about 1970. Previously the warmer temperatures induced wider rings. Most major warming and cooling trends are in agreement with other high-latitude temperature reconstructions based on tree-ring analyses with some regional differences in timing of cooling in the late 18th century and of warming in the late 19th century.     

Importance of seagrass as a carbon source for heterotrophic bacteria in a subtropical estuary (Florida Bay)

A stable carbon isotope approach was taken to identify potential organic matter sources incorporated into biomass by the heterotrophic bacterial community of Florida Bay, a subtropical estuary with a recent history of seagrass loss and phytoplankton blooms. To gain a more complete understanding of bacterial carbon cycling in seagrass estuaries, this study focused on the importance of seagrass-derived organic matter to pelagic, seagrass epiphytic, and sediment surface bacteria. Particulate organic matter (POM), seagrass epiphytic, seagrass (Thalassia testudinum) leaf, and sediment surface samples were collected from four Florida Bay locations with historically different organic matter inputs, macrophyte densities, and primary productivities. Bulk (observed and those reported previously) and compound-specific bacterial fatty acid δ¹³C values were used to determine important carbon sources to the estuary and benthic and pelagic heterotrophic bacteria. The δ¹³C values of T. testudinum green leaves with epiphytes removed ranged from −9.9 to −6.9‰. Thalassia testudinum δ¹³C values were significant more enriched in ¹³C than POM, epiphytic, and sediment samples, which ranged from −16.4 to −13.5, −16.2 to −9.6, and −16.7 to −11.0‰, respectively. Bacterial fatty acid δ¹³C values (measured for br14:0, 15:0, i15:0, a15:0, br17:0, and 17:0) ranged from −25.5 to −8.2‰. Assuming a −3‰ carbon source fractionation from fatty acid to whole bacteria, pelagic, epiphytic, and sediment bacterial δ¹³C values were generally more depleted in ¹³C than T. testudinum δ¹³C values, more enriched in ¹³C than reported δ¹³C values for mangroves, and similar to reported δ¹³C values for algae. IsoSource mixing model results indicated that organic matter derived from T. testudinum was incorporated by both benthic and pelagic bacterial communities, where 13–67% of bacterial δ¹³C values could arise from consumption of seagrass-derived organic matter. The IsoSource model, however, failed to discriminate clearly the fraction of algal (0–86%) and mangrove (0–42%) organic matter incorporated by bacterial communities. These results indicate that pelagic, epiphytic, and sediment surface bacteria consumed organic matter from a variety of sources. Bacterial communities incorporated consistently seagrass-derived organic matter, the dominant macrophyte in Florida Bay, but seagrass δ¹³C values alone could not account fully for bacterial δ¹³C values.     

How will climate change alter fishery governanceʔ Insights from seven international case studies

We examine the implications of climate change for fishery governance using seven international fishery case studies in low, mid and high latitudes, including eastern Australia, the western Pacific Ocean, Alaska, west coast United States, Hawaii, west coast Canada and France. Climate change adds uncertainty about fish stock productivity, migratory patterns, trophic interactions and vulnerability of fish populations to fishing pressure.     

海洋溢油鉴别前处理技术比较研究

针对目前海洋溢油样品的吸附色谱柱预分离前处理技术,比较了不同前处理方法得到的溢油样品中烃类化合物、生物标志物、金刚烷类化合物和多环芳烃类化合物的气相色谱／气相色谱质谱指纹图谱。就溢油样品吸附色谱柱预分离技术的优缺点进行了详细总结和讨论,并为溢油来源的快速、准确鉴别提出了建议。     

Comparing the Upper Triassic Deep-sea Flysch of theShannan Terrane with the Coeval Shallow Shelf Sediments ofthe Tethys Himalaya,Southern Tibet

The provenance and paleogeography of the Upper Triassic deep-sea flysch Langjiexue Group(LG) of the Shannan Terrane in the northeastern Himalaya orogen, south of Yarlung Zangbo, have been disputed in recent years since its affinity to the Tethys Himalaya was suspected during the early 2000 s. Based on the earlier discoveries of the Upper Permian–Triassic basalts and mafic dykes from the LG and of coeval detrital zircons from the Qulonggongba Formation(QF) in shallow shelf sediments of the Tethys Himalaya, the previous viewpoints on the basin and tectonics of the LG have been recently rejected. We compared the two units of the Upper Triassic, and our results reveal a number of differences,discrepancies, and inconsistencies in the debate, raising crucial questions on the postulation and provenance model of the remote Gondwanide Orogen for the LG. It is suggested that more observations and evidence are needed to further improve the paleogeographic understanding and relationship of the two units.     

陆相盆地中的海侵层序特征:中欧盆地三叠系与松辽盆地白垩系对比研究

中欧盆地三叠系是典型的海陆过渡相沉积，松辽盆地白垩系是含有海侵事件记录的陆相河湖盆地。两盆地的共同特点是：①大陆克拉通上长期发育的大型坳陷盆地；②靠近古大洋和（或）有向海通道；③主要由互层状泥岩、粉砂岩、碳酸盐岩和膏盐层组成；④无典型海相化石，可能发育有半咸水和（或）高盐度生物；⑤海侵层中自生矿物的δ^34S,δ^13C,δ^18O同位素比值及介质盐度指数（Sr/Ba）、碱度指数（Ca Mg)／（Si Al）、还原性指标（Zn Ni)/Ga、硫沉积通量指数（归一化硫含量）等显著高于相邻层位背景值。     

江汉平原长湖近代沉积物磁性测量及其气候意义

根据１９９２年长湖所取代表性９２－５ 面沉积物磁性测量结果并结合化学分析和孢粉分析,研究长湖近代沉积物磁性参数变化与气候变化的关系,指出该地区最近４００ａ来气候变化总趋势是一个由冷变暖的过程。     

A GCM study of future climate response to aerosol pollution reductions

We use the global atmospheric GCM aerosol model ECHAM5-HAM to asses possible impacts of future air pollution mitigation strategies on climate. Air quality control strategies focus on the reduction of aerosol emissions. Here we investigate the extreme case of a maximum feasible end-of-pipe abatement of aerosols in the near term future (2030) in combination with increasing greenhouse gas (GHG) concentrations. The temperature response of increasing GHG concentrations and reduced aerosol emissions leads to a global annual mean equilibrium temperature response of 2.18 K. When aerosols are maximally abated only in the Industry and Powerplant sector, while other sectors stay with currently enforced regulations, the temperature response is 1.89 K. A maximum feasible abatement applied in the Domestic and Transport sector, while other sectors remain with the current legislation, leads to a temperature response of 1.39 K. Increasing GHG concentrations alone lead to a temperature response of 1.20 K. We also simulate 2–5% increases in global mean precipitation among all scenarios considered, and the hydrological sensitivity is found to be significantly higher for aerosols than for GHGs. Our study, thus highlights the huge potential impact of future air pollution mitigation strategies on climate and supports the need for urgent GHG emission reductions. GHG and aerosol forcings are not independent as both affect and are influenced by changes in the hydrological cycle. However, within the given range of changes in aerosol emissions and GHG concentrations considered in this study, the climate response towards increasing GHG concentrations and decreasing aerosols emissions is additive.     

Progressive oxidation of pyrite in five bituminous coal samples: An As XANES and Fe Mössbauer spectroscopic study

Naturally occurring pyrite commonly contains minor substituted metals and metalloids (As, Se, Hg, Cu, Ni, etc.) that can be released to the environment as a result of its weathering. Arsenic, often the most abundant minor constituent in pyrite, is a sensitive monitor of progressive pyrite oxidation in coal. To test the effect of pyrite composition and environmental parameters on the rate and extent of pyrite oxidation in coal, splits of five bituminous coal samples having differing amounts of pyrite and extents of As substitution in the pyrite, were exposed to a range of simulated weathering conditions over a period of 17 months. Samples investigated include a Springfield coal from Indiana (whole coal pyritic S = 2.13 wt.%; As in pyrite = detection limit (d.l.) to 0.06 wt.%), two Pittsburgh coal samples from West Virginia (pyritic S = 1.32–1.58 wt.%; As in pyrite = d.l. to 0.34 wt.%), and two samples from the Warrior Basin, Alabama (pyritic S = 0.26–0.27 wt.%; As in pyrite = d.l. to 2.72 wt.%). Samples were collected from active mine faces, and expected differences in the concentration of As in pyrite were confirmed by electron microprobe analysis. Experimental weathering conditions in test chambers were maintained as follows: (1) dry Ar atmosphere; (2) dry O₂ atmosphere; (3) room atmosphere (relative humidity ∼20–60%); and (4) room atmosphere with samples wetted periodically with double-distilled water. Sample splits were removed after one month, nine months, and 17 months to monitor the extent of As and Fe oxidation using As X-ray absorption near-edge structure (XANES) spectroscopy and ⁵⁷Fe Mössbauer spectroscopy, respectively. Arsenic XANES spectroscopy shows progressive oxidation of pyritic As to arsenate, with wetted samples showing the most rapid oxidation. ⁵⁷Fe Mössbauer spectroscopy also shows a much greater proportion of Fe³⁺ forms (jarosite, Fe³⁺ sulfate, FeOOH) for samples stored under wet conditions, but much less difference among samples stored under dry conditions in different atmospheres. The air-wet experiments show evidence of pyrite re-precipitation from soluble ferric sulfates, with As retention in the jarosite phase. Extents of As and Fe oxidation were similar for samples having differing As substitution in pyrite, suggesting that environmental conditions outweigh the composition and amount of pyrite as factors influencing the oxidation rate of Fe sulfides in coal.