The exchange of organic carbon in basin mangrove forests in a southwest Florida estuary

The magnitude and seasonality of organic carbon exchange was estimated for two basin mangrove forests in Rookery Bay, Florida. Runoff and tidal inundation in the forests were seasonal with half the annual total of each occurring from August to October. In each forest there were 152 tides yr^?1 with a cumulative depth of about 12 m. Total organic carbon increased in bay waters exporting from the mangroves following a flood tide and peak concentrations were associated with export due to rainfall. The amount of net export from each basin forest was similar, although the concentration of organic carbon in each were different. Monthly net organic carbon export was proportional to the cumulative tidal amplitude within the forest. Total organic carbon export was 64 gC m^?2 yr^?1 and DOC was 75% of the total. A comparison of organic carbon export among riverine, fringe and basin mangroves suggests that tidal hydrology influences the proportion of litter fall that is exported from mangroves; and the magnitude of this organic carbon export from mangroves is related to the cumulative tidal amplitude within the forests.     

Dissolved organic carbon dynamics in two streams draining forested catchments at loch ard,Scotland

Dissolved organic carbon (DOC) was measured at four or eight hour intervals between mid-1989 and mid-1991 in two catchments in west central Scotland. The experimental catchment had been recently clear-felled and the control remained under forest. The amount of DOC varied during individual storm events following the stream hydro-graph. Maximum variations were found in the summer half-year and in the clear-felled catchment. There was also evidence of the exhaustion of DOC in the later events of a sequence. Differences between the catchments were related to catchment characteristics and to land-use change. The reduced magnitude of variation in DOC with discharge in the control stream was due to the influence of a wetland area through which the stream flowed. The mean DOC concentrations were similar in the two streams and annual exports were 15 g m^?2 from the control and 16g m^?2 from the felled catchment. The stream draining the clear-felled catchment had greater high flow DOC concentrations in the summer half-year, probably due to the effect of greater mean summer temperatures on DOC release and of the greater supply of organic debris in the stream channel.     

沙坡头没蒿和柠条叶片δ13C 和 N 含量的季节变化特征

通过对腾格里沙漠东南缘沙坡头人工固沙区油蒿和柠条叶片稳定碳同位素分辨率（△）和N 含量的测定，研究了不同种植方式下油蒿和柠条叶片△ 和 N 含量的季节变化及其关系。结果表明：在不同种植方式下，两种植物的△ 与 N 含量在不同月份之间均存在显著差异。油蒿叶片 △ 极显著高于柠条的：在不同种植方式下，油蒿单种下 △ 显著高于混种，柠条则反之。 油蒿叶片 N 含量极显著低于柠条的：不同种植方式下柠条叶片 N 含量无显著差异，而单种油蒿叶片 N 含量则显著低于混种。在 △ 与 N 含量的关系中，柠条叶片 △ 与 N 在两种生境、单种和混种下均极显著正相关，雨明柠条叶片 N 含量可以作为其 △ 与 N 含量的季节变化及其关系在不同微生境有所差异。     

有机碳同位素示踪古环境变化研究

对有机碳同位素示踪环境变化的原理、研究对象、取得的进展和存在的问题等进行了详细研究，认识到C～H键比C-O键有利于富集^12C，从而导致生物或有机碳δ^13C为极低的负值，使有机碳与无机碳之间存在显著的碳同位素差异。光合作用类型的不同使植物分为C3，C4和CAM3种类群，并导致不同类群的植物具有不同的碳同位素组成，C3植物δ^13C=-20‰～-32‰，平均-28‰，而C4植物δ^13C=-9‰～-17‰，平均-14‰。气候环境的差异影响了光合作用的类型和强度，使不同环境的植物类群特征不同，不仅造成植物组合的碳同位素组成不同，而且导致不同食性的动物牙齿等化石的碳同位素组成的差异，甚至相应的无机碳同位素的变化，因此生物链及其衍生物的碳同位素研究也就成为反演某一地区或某一时期气候环境的有效手段。被作为研究对象的地质记录可分为有机和无机两类，有机类主要包括树轮等植物化石、牙齿等动物化石、煤等陆相沉积有机质、海相沉积有机质、土壤(前者的衍生物)，这些研究对象分别适合于目的不同的环境研究，并获得了较好的效果。进而发现有机碳同位素在研究重大生物灭绝事件、C4植物起源、地球早期生命起源、地外生命存在与否、矿产资源形成时的有机质作用等问题上将有重要作为。     

HITRAN数据库对卫星1.6 μm通道CO2辐射传输特性计算的影响

卫星遥感器中的CO21.6μm弱吸收带通道测量信号可以反映CO2的近地层浓度分布,是温室气体卫星反演的重要通道之一。HITRAN数据库是建立卫星遥感CO2浓度算法依赖的重要分子光谱参数数据库,目前已经更新到了2012版,不同版本中大气分子谱线参数存在差异。本文利用逐线积分模式LBLRTM,研究了最近3个版本HITRAN数据库(04、08、12版)在CO2的弱吸收带通道上大气光学厚度、透过率的差异,发现04版计算的气体光学厚度普遍偏高,可对CO2造成约38 ppm的低估;08版本得到的气体光学厚度与12版本接近,反演相差2 ppm以内。在此基础上,分析了不同HITRAN数据库对整层CO2变化和近地层CO2变化的敏感性,结果表明:04版对整层和近地面大气的变化敏感性最强,并且放大了近地层信号;08版与12版对整层或近地层CO2的敏感度接近,两者经过卷积后得到的信号无差异。     

平顶山城区碳环境演变时间序列分析

大气中日益上升的温室气体浓度,已导致温室效应日益增强,从而引发一系列不利的环境与生态后果,并会对世界粮食生产、水资源利用等关系人类生存发展的方面产生重要影响。1994~2014年是平顶山城市化进程不断加快和经济社会高速发展的时期,土地利用、人口、能源消耗和城市植被等影响碳源、碳汇的主要方面也都发生了重大的变化。将1994~2014年河南省平顶山市城区的碳平衡变化情况作为研究对象,计算出碳平衡主要影响因素各自的变化情况并加以分析,得出有关平顶山城区碳环境演变的结论。最后,为促进平顶山城区的碳源碳汇平衡,提出实现城市快速发展过程中低碳效应策略。     

Applying personal carbon trading: a proposed ‘Carbon,Health and Savings System’ for British Columbia,Canada

Addressing climate change requires the synergy of technological, behavioural and market mechanisms. This article proposes a policy framework that integrates the three, deploying personal carbon trading as a key element within a policy portfolio to reduce personal carbon footprints. It draws on policy and human motivation literatures that address the behavioural changes that may be needed in the context of a long-term threat such as climate change. This proposal builds on an analysis of the British Columbia carbon tax, international examples of carbon pricing instruments and strategies for behavioural change such as social networks, loyalty management, mobile apps and gamification. Interviews were conducted with experts in financial services, energy conservation and clean technology, as well as with specialists in climate, health and taxation policy. Their input, together with a review of the theoretical literature and practical case studies, informed the proposed design of a Carbon, Health and Saving System for promoting individual engagement and collective action by linking long-term climate mitigation measures with short-term personal and social goals, including health, recreation and social reinforcement.

Policy Relevance

This article identifies areas for climate policy innovation and recommends policies that can support, promote and enable personal carbon budgeting and collective action. Although this study is focused on British Columbia, both the input provided by key opinion leaders and the proposed framework are applicable to other jurisdictions.

This policy proposal shows how personal carbon trading could work in the context of a Canadian province with an existing climate mitigation policy. It also specifies a minimum viable product approach to establishing the economic, social and technological foundations for personal carbon trading.

The Carbon, Health and Saving System identifies the technologies and stakeholders needed to implement personal carbon trading, and offers the possibility of motivating a widespread conscious human response in the event that carbon taxation proves insufficient to generate economic adaptation in a changing climate.     

Carbon and Noble Gas Isotopes in the Tengchong Volcanic Geothermal Area, Yunnan, Southwestern China

Carbon and noble gas isotope analyses are reported for bubbling gas samples from the Tengchong volcanic geothermal area near the Indo-Eurasian suture zone. All samples contain a resolvable component of mantle-derived 3He. Occurrence of mantle-derived 3He coincides with surface volcanism. However, 3He occurs over a larger geographic areathan do surface volcanics. δ13C values for CO2 and CH4 vary from -33.4‰ to 1.6 ‰ and from -52.8‰ to -2.8‰, respectively. He and C isotope systematics indicate that CO2 and CH4 in the CO2-rich gases originated predominantly from magmatic component mixed with crustal CO2 produced from carbonate. However, breakdown of organic matter and near-surface processes accounts for the CH4 and CO2 in N2-rich gases. 3He/4He ratio distribution pattern suggests that mantle-derived He and heat sources of high-temperature system in central Tengchong originate from a hidden magma reservoir at subsurface. CO2-rich gases with the highest 3He/4He ratio (5.2 Ra) may be representative of the     

沁水盆地南部潘庄区块废弃矿井煤层气地球化学特征及成因

为了研究废弃矿井中煤层气成因,以沁水盆地南部潘庄区块废弃矿井为例,抽采废弃矿井中煤层气并进行化学组分和同位素测试,并采集部分废弃矿井水样品测试水中离子浓度、pH值等进行研究。结果表明：潘庄区块废弃矿井中煤层气CH₄体积分数平均值为91.99%,CO₂为1.26%,N₂为6.73%;甲烷碳同位素（δ¹³C₁）值为-31.36‰~-33.53‰,平均-32.25‰,氢同位素（δD）值为-182.76‰~-193.20‰,平均-187.538‰。废弃矿井排采水中阴阳离子主要为Mg²⁺、K⁺、HCO₃^-、Cl^-、Na⁺、SO₄^2-和NO₃^-等,产出水型为Mg-（HCO₃）₂型,表明矿井水受到地表水的强烈影响。废弃矿井中煤层气主要以热成因气为主,少量次生生物气。与附近未开采煤储层相比,研究区废弃矿井中的环境更有利于次生生物气的生成。     

Chemical Characteristics of Carbonaceous Aerosols During Dust Storms over Xi＇an in China

Characterization of carbonaceous aerosols including CC (carbonate carbon), OC (organic carbon), and EC (elemental carbon) were investigated at Xi'an, China, near Asian dust source regions in spring 2002. OC varied between 8.2 and 63.7 μg m-3, while EC ranged between 2.4 and 17.2 μ m-3 during the observation period. OC variations followed a similar pattern to EC and the correlation coeflcient between OC and EC is 0.89 (n=31). The average percentage of total carbon (TC, sum of CC, OC, and EC) in PM2.5 during dust storm (DS) events was 13.6%, which is lower than that during non-dust storm (NDS) periods (22.7%). CC, OC, and EC accounted for 12.9%, 70.7%, and 16.4% of TC during DS events, respectively. The average ratio of OC/EC was 5.0 in DS events and 3.3 in NDS periods. The OC-EC correlation (R2=0.76, n=6) was good in DS events, while it was stronger (R2=0.90, n=25) in NDS periods. The percentage of water-soluble OC (WSOC) in TC accounted for 15.7%, and varied between 13.3% and 22.3% during DS events. The distribution of eight carbon fractions indicated that local emissions such as motor vehicle exhaust were the dominant contributors to carbonaceous particles. During DS events, soil dust dominated the chemical composition, contributing 69% to the PM2.5 mass, followed by organic matter (12.8%), sulfate (4%), EC (2.2%), and chloride (1.6%). Consequently, CC was mainly entrained by Asian dust. However, even in the atmosphere near Asian dust source regions, OC and EC in atmospheric dust were controlled by local emission rather than the transport of Asian dust.