张广才岭西坡45年生不同起源林分碳储量研究

以五常凤凰山林场皆伐迹地上45年生不同起源(人工造林、人天混更新、天然更新)形成的落叶松纯林、落叶松与阔叶树混交林和次生阔叶林3种林分为研究对象,调查分析不同林型林分乔木层、灌草层、凋落物层、土壤层碳储量以及3种林型林分总碳储量,分析不同更新方式对森林碳储量的影响,探究具有高固碳能力的森林更新方式。研究结果表明:人天混交林能增加林分灌草层碳储量(P<0.05);凋落物未分解层碳储量、半分解层碳储量和凋落物总碳储量均以落叶松纯林最高,且半分解层碳储量和凋落物总碳储量在3个林型间差异显著(P<0.05);土壤总碳储量以及森林生态系统总碳储量针阔混交林均略高于其它两种林分,但差异并不显著(P>0.05)。研究表明人天混更新有利于植被碳汇和土壤碳汇能力的提高。人工针叶纯林具有较高的凋落物碳储量。     

不同退化沙地土壤碳的矿化潜力

通过实验室土壤培养试验 ,研究了科尔沁退化沙质草地不同生境 (流动沙地 ,半固定沙地 ,固定沙地和丘间低地 )下土壤碳的矿化潜力及不同凋落物在沙地土壤中的分解。经 33d的室内培养 ,不同生境土壤 CO2 - C的释放有极显著的差异 ,与生境植被盖度 ,凋落物积累 ,土壤沙化程度 ,土壤有机碳和全氮含量的分布有显著相关。流动沙地土壤有极低的土壤有机碳和氮的含量及其微弱的土壤微生物呼吸 ,表明土地沙漠化不仅导致土壤有机碳库衰竭 ,也使土壤微生物活性丧失。在有机质含量很低的流动沙地和半固定沙地土壤中 ,含氮量高的小叶锦鸡儿 (Caragana microphylla)凋落物比含氮量低、C/N比高的差巴嘎蒿(Artemisia halodendron)和 1年生植物凋落物有较快的分解。在沙漠化的演变中 ,土壤的粗粒化 ,有机物质和养分及微生物活性的丧失制约着凋落物在土壤中的矿化潜力。灌木的存在使更多的有机物质和养分积聚在灌丛下 ,形成灌丛肥岛 ,因而显著贡献于碳的固存。     

碳输入方式对森林土壤碳库和碳循环的影响研究进展

凋落物和植物根系是森林土壤有机碳的主要来源.综述了不同碳输入方式对土壤全碳、微生物生物量碳和可溶性有机碳等碳库组分及土壤呼吸影响的研究进展.不同地区、不同森林土壤有机碳对碳输入的响应程度不同,且采用添加和去除凋落物,以及去除根系方法(DIRT)对土壤碳的影响具有树种差异和区域差异.目前主要侧重于土壤呼吸和碳库组分的研究,亟需开展对土壤碳的结构类型和稳定性,以及土壤生物尤其是土壤动物的响应机制的相关研究.     

鼎湖山亚热带常绿针阔叶混交林凋落物及矿质氮输入对土壤有机碳分解的影响

2010年7-12月,选取鼎湖山国家级自然保护区亚热带针阔叶混交林,采用全因子控制试验,研究不同类型的凋落物(针叶和阔叶凋落物)添加及氮处理(加氮模拟氮饱和、减氮模拟根吸收)对表层(0～10 cm)和下层(20～30 cm)土壤有机质分解(呼吸)的影响.结果表明： 2010年7-11月间,两种凋落物的添加使土壤-凋落物系统的呼吸速率显著增加,但这种影响在12月消失.减氮和加氮处理均显著增加了土壤-凋落物系统的呼吸.叶凋落物短期内完全分解,对土壤碳分解和积累的影响十分有限,可能不是该系统中土壤有机质的主要来源.通过减少土壤可利用氮模拟根系对氮的吸收能够明显促进土壤有机质的分解.     

不同植被配置下土壤碳矿化潜力

通过实验室培养的方法,研究了沙坡头地区不同植被配置区(纯柠条、纯油蒿、柠条油蒿混交林)土壤碳矿化潜力及不同凋落物在土壤中的分解.结果表明,通过103 d的室内培养,相同配置不同处理的土壤碳矿化差异不显著,灌丛密度高的植被配置碳矿化量高.不同生境土壤CO2-C的释放在灌丛下不加凋落物处理的情况下,单行油蒿与双行柠条样地间碳矿化存在显著性差异(P=0.047),其他各样地及各处理差异均不显著.总的来说,柠条样地土壤碳矿化潜力高于其他2种样地.凋落物分解速率在不同生境土壤最初的分解速率均为1年生草本混合样＞油蒿＞柠条,在培养40 d之后,3种凋落物的分解速率趋于一致,这与草本较高的C、N、C/N比有关.另外,柠条样地的土壤加油蒿凋落物比在柠条样地的土壤中加柠条凋落物有较高的初始碳矿化潜力,这除与油蒿凋落物较易分解有关外还与不同生境土壤养分的可利用性有关,但在培养过程中出现拐点,这与柠条较高的C、N、C/N有关.在不同生境的土壤中,碳矿化潜力均为灌丛下＞灌丛外,灌木的存在使更多的有机质和养分积聚在灌丛下,形成灌丛肥岛,对碳的固存具有显著贡献.     

中国森林的地下碳分配

通过收集国内33个森林样地的土壤呼吸和年凋落物量数据,分析中国森林地下碳分配（TBCA）模式。结果表明,中国森林土壤呼吸年通量与年凋落物量呈显著的线性相关（R^2=0．3319,P=0．000）,其中成熟林土壤呼吸与年凋落物量间呈显著的线性相关（R^2=0．3245,P=0．004）,但未成熟林土壤呼吸与年凋落物量间的线性相关不显著（R^2=0．3485,P=0．092）。中国森林的地下碳分配变化范围1．460～25．100tChm^-2a^-1,平均值为9．217tChm^-2a^-1;中国森林的TBCA与年均气温相关关系不显著（P=0．196）,但与年均降水量则呈显著正相关（R=0．480,P=0．021）。中国森林TBCA和凋落物对土壤呼吸的平均贡献分别为74．2％和25．8％;中国森林TBCA对土壤呼吸的贡献随土壤呼吸增大而增大,而凋落物对土壤呼吸的贡献则随土壤呼吸的增大而降低。     

万木林自然保护区不同林分土壤可溶性有机氮含量

对福建建瓯万木林自然保护区内细柄阿丁枫天然林(ALG)、米槠天然林(CAC)和35年生杉木人工林(CUL)土壤可溶性有机氮含量(SON)进行了研究.结果表明:3种林分中,ALG0～5cm、5～10cm和10～20cm层土壤SON含量最高,分别为95.3、78.3和72.5mg.kg-1,且与其余林分差异显著(P0.05);而CAC与CUL各土层SON含量分别为74.5、70.1、65.6mg.kg-1和78.6、68.9、69.1mg.kg-1.CAC、CUL和ALG在0～20cm土层的SON含量分别占可溶性总氮(TSN)组分的79.17%～80.78%、68.64%～74.51%和59.97%～69.66%,随着土层加深,3种林分SON含量占土壤TSN和全氮(TN)含量的比例不断增大;SON与土壤有机碳含量极显著相关(r=0.982,P0.01),与TSN、TN、铵态氮和硝态氮等土壤养分也存在不同程度的相关性.土壤SON含量与森林类型、地形、海拔以及树龄等因素有关.     

草地利用方式对土壤呼吸和凋落物分解的影响

草地利用方式影响植被群落结构和土壤微环境, 制约草地生态系统碳循环。该文通过测定温带草原在放牧、割草、围封3种利用方式下湿润年(2012年)和干旱年(2011年)的凋落物产量、质量及其分解速率和土壤碳通量, 分析了草地利用方式对土壤呼吸和凋落物的影响, 探讨了凋落物对土壤呼吸的贡献机制。结果表明: 在干旱年份, 放牧样地土壤呼吸最大, 分别达到割草和围封样地的1.5倍和1.29倍; 在湿润年份, 割草样地土壤呼吸最大, 为309 g C∙m^-2∙a^-1, 明显高于放牧样地和围封样地。不论干旱年还是湿润年, 围封样地凋落物产量都大于放牧样地和割草样地。3种利用方式下湿润年土壤呼吸和凋落物分解均比干旱年增强。因此, 水分是温带草原植物生长和生态系统碳循环的主要限制因子, 草地利用方式则显著影响凋落物生产和分解。进一步分析表明, 经过两年的分解, 同一样地内凋落物质量C:N下降, N含量和木质素:N升高, 土壤呼吸与凋落物产量、凋落物分解速率以及木质素:N正相关, 而与凋落物C:N负相关。     

黄土旱塬区冬小麦不同施肥处理的土壤呼吸及土壤碳动态

依据黄土旱塬区黑垆土上中国科学院长武站长期定位试验 (始于1984年),于2008年3月到6月,测定了冬小麦连作系统中返青期、拔节期、抽穗期、灌浆期和收获期土壤呼吸日变化、生育期变化以及土壤可溶性有机碳(Dissolved organic C, DOC)和微生物量碳(Soil microbial biomass C, MBC),研究了施肥措施对土壤呼吸、DOC和MBC的影响以及土壤呼吸与碳组分之间的关系.研究涉及6个处理:休闲地(F)、不施肥(CK)、有机肥(M)、氮肥(N)、氮磷肥(NP)和氮磷有机肥(NPM).结果表明,冬小麦连作系统中土壤呼吸的日变化格局呈单峰曲线,最高值出现在12:00左右(拔节期)和14:30左右(成熟期),最小值出现在0:00～3:00之间或6:00左右;冬小麦土壤呼吸速率拔节期最高,其次是灌浆后期,抽穗期最低;不同施肥条件下,各生育期土壤呼吸速率大小顺序:NPM＞M＞NP＞N＞CK＞F.土壤水分亏缺是导致抽穗期和灌浆期土壤呼吸速率降低的重要原因.各施肥处理DOC含量高低顺序为灌浆期＞抽穗期＞成熟期＞返青期＞拔节期;除M,NPM处理MBC含量拔节期＞灌浆期外,各施肥处理MBC含量高低顺序为成熟期＞抽穗期＞灌浆期＞拔节期＞返青期.同一处理不同生育期土壤呼吸速率与DOC,MBC的相关性较低,但同生育期不同施肥处理土壤呼吸与土壤有机碳组分间存在显著的相关性.以F处理土壤呼吸为基础,估算CK、N和NP处理生育期根系对土壤呼吸的平均贡献率依次为36%、45%和54%.     

不同起源时间的植物叶凋落物在中亚热带的分解特性

选择9种起源时间不同的植物的凋落叶,采用分解袋法,在浙江千岛湖地区从2006年6月到2008年6月进行了分解试验,试图探索植物进化过程中凋落物分解特性的演变趋势.所选的9种植物分属于4个类群,按起源时间由早到晚依次为蕨类植物(芒萁和桫椤)、裸子植物(苏铁、水杉、杉木和马尾松)、双子叶植物(木荷和青冈)及单子叶植物(毛竹).每隔一个月取样,每种凋落物3次重复.结果表明:不同植物类群凋落物基质的氮(N)、木质素(Lignin)含量及Lignin/N比值与分解速率具有良好的相关性.起源时间越晚的植物凋落物的基质N含量越高,为单子叶植物>双子叶植物>裸子植物>蕨类植物.Lignin含量和Lignin/N比值的趋势一致,均为起源时间越晚而值越低,即蕨类植物>裸子植物>双子叶植物>单子叶植物.凋落物分解系数k值的范围在0.25～0.63之间,表现出毛竹>青冈>木荷>水杉>马尾松>杉木>苏铁>桫椤>芒萁的趋势.4个植物类群的凋落物分解速率的均值为单子叶植物>双子叶植物>裸子植物>蕨类植物.试验结果初步表明:植物凋落物分解的进化趋势是由分解缓慢逐渐演变为分解较快.     

Different types of nitrogen deposition show variable effects on the soil carbon cycle process of temperate forests

Nitrogen (N) deposition significantly affects the soil carbon (C) cycle process of forests. However, the influence of different types of N on it still remained unclear. In this work, ammonium nitrate was selected as an inorganic N (IN) source, while urea and glycine were chosen as organic N (ON) sources. Different ratios of IN to ON (1 : 4, 2 : 3, 3 : 2, 4 : 1, and 5 : 0) were mixed with equal total amounts and then used to fertilize temperate forest soils for 2 years. Results showed that IN deposition inhibited soil C cycle processes, such as soil respiration, soil organic C decomposition, and enzymatic activities, and induced the accumulation of recalcitrant organic C. By contrast, ON deposition promoted these processes. Addition of ON also resulted in accelerated transformation of recalcitrant compounds into labile compounds and increased CO₂ efflux. Meanwhile, greater ON deposition may convert C sequestration in forest soils into C source. These results indicated the importance of the IN to ON ratio in controlling the soil C cycle, which can consequently change the ecological effect of N deposition.     

东北松嫩平原羊草群落的土壤呼吸与枯枝落叶分解释放CO2贡献量

根据静态气室法的测量结果 ,分析了羊草群落土壤呼吸量和枯枝落叶分解释放 CO2 量的季节动态 ,及其与地上生物量 ,枯枝落叶分解量及环境因子的关系。结果表明 :( 1 )在整个观测期内 ,羊草群落土壤呼吸的季节动态呈现单峰曲线 ,8月中旬达到最大值 1 3.2 7g C/( m2 · d)。 ( 2 )羊草群落土壤呼吸的季节变化规律与地上绿色体生物量的季节动态同步。( 3)羊草群落土壤呼吸的季节动态与枯枝落叶分解量的季节动态同步。 ( 4 )羊草群落土壤呼吸量与土壤 0～ 1 0 cm土壤含水量显著正相关。( 5 )地表枯枝落叶层直接排放 CO2 量的季节动态呈现逐渐递减的趋势 ,释放量平均为 -0 .87g C/( m2·d)。有减缓土壤向大气排放 CO2 的作用。 ( 6 )枯枝落叶分解释放 CO2 量同地表枯枝落叶量显著正相关。     

小兴安岭4种原始红松林群落类型生长季土壤呼吸特征

为阐明小兴安岭地带性植被原始红松林土壤呼吸各组分的碳排放速率及其对土壤水热变化的响应规律,采用挖壕法和红外气体分析法测定土壤表面CO2通量(Rs),确定4种原始红松林群落类型生长季的土壤总呼吸(Rt)中土壤微生物呼吸(Rh),根系呼吸(Rr)和凋落物呼吸(Rl)的贡献量动态变化及其影响因子。结果表明:生长季内,4种原始红松林群落类型的Rt、Rh、Rr具有明显的季节性变化,7-9月份较高,6月份和10月份较低。Rh对Rt的贡献量最高,平均在58.8%;Rr对Rt的贡献量次之,平均为26.5%;Rl对Rt的贡献量相对较小,平均为12.5%。生长季土壤呼吸速率与5cm深土壤温度相关性极显著(P0.01)。Rr和Rh的Q10值分别为2.88和2.23。表明根呼吸对土壤温度的敏感性高于微生物呼吸。生长季平均土壤呼吸速率的依次为:椴树红松林(6.38μmol·m-·2s-1)云冷杉红松林(6.32μmol·m-·2s-1)枫桦红松林(5.95μmol·m-·2s-1)蒙古栎红松林(2.86μmol·m-·2s-1)。4种原始叶红松林群落类型间的Rh和Rr也存在一定差异。     

黑龙江省帽儿山林区6种主要林分类型凋落物研究

对帽儿山林区水曲柳、落叶松等六种主要林分的年凋落量、凋落物组成及分解动态进行了观测。结果表明：(1) 六种林分的年凋落量分别为水曲柳(5.57 t·hm^-2)、蒙古栎(4. t·hm^-2)、山杨(4.27 t·hm^-2)、落叶松(4.08 t·hm^-2)、红松(5.62 t·hm^-2)、樟子松(5.56 t·hm^-2);(2) 六种林分其叶的年凋落量占年总凋落量的比例明显大于其它组分,是其凋落物中的主要组成部分;(3) 经过近1a时间的分解,测得六种林分凋落叶分解速率依次为：水曲柳>樟子松>落叶松>山杨>蒙古栎>红松;经模拟研究表明,水曲柳凋落叶95%分解需3.5 a;蒙古栎需8.0 a;山杨需6.7 a;落叶松需6.6 a;红松需8.8 a;樟子松需4.4 a。     

Soil respiration in six temperate forests in China

Scaling soil respiration (R_S), the major CO₂ source to the atmosphere from terrestrial ecosystems, from chamber‐based measurements to ecosystems requires studies on variations and correlations of R_S from various biomes and across geographic regions. However, few studies on R_S are available for Chinese temperate forest despite the importance of this forest in the national and global carbon budgets. In this study, we conducted 18‐month R_S measurements during 2004–2005 in six temperate forest types, representing the typical secondary forest ecosystems across various site conditions in northeastern China: Mongolian oak (Quercus mongolica Fisch.), aspen‐birch (Populous davidiana Dode and Betula platyphylla Suk.), mixed deciduous (no dominant tree species), hardwood (dominated by Fraxinus mandshurica Rupr., Juglans mandshurica Maxim., and Phellodendron amurense Rupr.) forests, Korean pine (Pinus koraiensis Sieb. et Zucc.) and Dahurian larch (Larix gmelinii Rupr.) plantations. Our specific objectives were to: (1) explore relationships of R_S against soil temperature and water content for the six forest ecosystems, (2) quantify annual soil surface CO₂ flux and its relations to belowground carbon storage, (3) examine seasonal variations in R_S and related environmental factors, and (4) quantify among‐ and within‐ecosystem variations in R_S. The R_S was positively correlated to soil temperature in all forest types, and was significantly influenced by the interactions of soil temperature and water content in the pine, larch, and mixed deciduous forests. The sensitivity of R_S to soil temperature at 10 cm depth (Q₁₀) ranged from 2.61 in the oak forest to 3.75 in the aspen‐birch forests. The Q₁₀ tended to increase with soil water content until reaching a threshold, and then decline. The annual R_S for the larch, pine, hardwood, oak, mixed deciduous, and aspen‐birch forests averaged 403, 514, 781, 785, 786, and 813 g C m^?2 yr^?1, respectively. The annual R_S of the broadleaved forests was 72% greater than that of the coniferous forests. The annual R_S was positively correlated to soil organic carbon (SOC) concentration at O horizon (R²=0.868) and total biomass of roots <0.5 cm in diameter (R²=0.748). The coefficient of variation (CV) of R_S among forest types averaged 25% across the 18‐month measurements. The CV of R_S within plots varied from 20% to 27%, significantly (P<0.001) greater than those among plots (9–15%), indicating the importance of the fine‐scaled heterogeneity in R_S. This study emphasized that variations in soil respiration and potential sampling bias should be appropriately tackled for accurate soil CO₂ flux estimates.     

Annual variation in soil respiration and its components in a coppice oak forest in Central Italy

In order to investigate the annual variation of soil respiration and its components in relation to seasonal changes in soil temperature and soil moisture in a Mediterranean mixed oak forest ecosystem, we set up a series of experimental treatments in May 1999 where litter (no litter), roots (no roots, by trenching) or both were excluded from plots of 4 m². Subsequently, we measured soil respiration, soil temperature and soil moisture in each plot over a year after the forest was coppiced. The treatments did not significantly affect soil temperature or soil moisture measured over 0–10 cm depth. Soil respiration varied markedly during the year with high rates in spring and autumn and low rates in summer, coinciding with summer drought, and in winter, with the lowest temperatures. Very high respiration rates, however, were observed during the summer immediately after rainfall events. The mean annual rate of soil respiration was 2.9 µ mol m^?2 s^?1, ranging from 1.35 to 7.03 µmol m^?2 s^?1. Soil respiration was highly correlated with temperature during winter and during spring and autumn whenever volumetric soil water content was above 20%. Below this threshold value, there was no correlation between soil respiration and soil temperature, but soil moisture was a good predictor of soil respiration. A simple empirical model that predicted soil respiration during the year, using both soil temperature and soil moisture accounted for more than 91% of the observed annual variation in soil respiration. All the components of soil respiration followed a similar seasonal trend and were affected by summer drought. The Q₁₀ value for soil respiration was 2.32, which is in agreement with other studies in forest ecosystems. However, we found a Q₁₀ value for root respiration of 2.20, which is lower than recent values reported for forest sites. The fact that the seasonal variation in root growth with temperature in Mediterranean ecosystems differs from that in temperate regions may explain this difference. In temperate regions, increases in size of root populations during the growing season, coinciding with high temperatures, may yield higher apparent Q₁₀ values than in Mediterranean regions where root growth is suppressed by summer drought. The decomposition of organic matter and belowground litter were the major components of soil respiration, accounting for almost 55% of the total soil respiration flux. This proportion is higher than has been reported for mature boreal and temperate forest and is probably the result of a short‐term C loss following recent logging at the site. The relationship proposed for soil respiration with soil temperature and soil moisture is useful for understanding and predicting potential changes in Mediterranean forest ecosystems in response to forest management and climate change.     

东灵山地区辽东栎林主要土壤因子的Haar小波分解

小波分解可以区分一维信号的区域变化和局部细节,是进行土壤因子分析的一种有效方法。应用该方法对北京东灵山地区辽东栎林样带中的3个主要土壤因子指标进行Haar小波分解。结果表明：沿山下到山顶样带梯度,土壤含水量呈明显的逐步下降趋势;土壤pH值变化幅度在6.5-6.6之间,表现比较稳定;土壤有机质含量在样带中存在3个较高值区域,具有一定的复杂性。较大水平上3个土壤因子在样带的下部受到的干扰较大,在样带的中、上部受到的干扰较小;在较小水平上,土壤含水量存在不规则的周期性干扰,pH值和有机质含量受干扰的情况较为复杂,规律性不明显。低频近假信号可以有效地揭示出土壤因子在样带中的总体变化规律,高频细节信号主要反映土壤因子受其它因素干扰程度,并可以在样带上定位出现奇异性变化的区域。     

Seasonal changes in the contribution of root respiration to total soil respiration in a cool-temperate deciduous forest

A trenching method was used to determine the contribution of root respiration to soil respiration. Soil respiration rates in a trenched plot (R _trench) and in a control plot (R _control) were measured from May 2000 to September 2001 by using an open-flow gas exchange system with an infrared gas analyser. The decomposition rate of dead roots (R _D) was estimated by using a root-bag method to correct the soil respiration measured from the trenched plots for the additional decaying root biomass. The soil respiration rates in the control plot increased from May (240–320 mg CO₂ m^–2 h^–1) to August (840–1150 mg CO₂ m^–2 h^–1) and then decreased during autumn (200–650 mg CO₂ m^–2 h^–1). The soil respiration rates in the trenched plot showed a similar pattern of seasonal change, but the rates were lower than in the control plot except during the 2 months following the trenching. Root respiration rate (R _r) and heterotrophic respiration rate (R _h) were estimated from R _control, R _trench, and R _D. We estimated that the contribution of R _r to total soil respiration in the growing season ranged from 27 to 71%. There was a significant relationship between R _h and soil temperature, whereas R _r had no significant correlation with soil temperature. The results suggest that the factors controlling the seasonal change of respiration differ between the two components of soil respiration, R _r and R _h.