最近12000年来青藏高原植被的时空分布

青藏高原 30个点湖泊的孢粉记录综合研究显示 :在进入全新世之前 (12kaBP以前 ) ,除最东南部外 ,高原从东到西均发育为荒漠草原植被。全新世早期 (12 .0 - 9.0kaBP)高原东南部 (10 4° - 98°E)为落叶阔叶林 /针阔叶混交林 ;中部 (98° - 92°E)为草甸或灌丛草甸 ,再向西至 80°E左右为草原植被 ;全新世中期 (9.0 - 3 .2kaBP)高原由东向西古植被依次发育为针阔混交林和硬叶阔叶林 (10 4° - 98°E)→针阔混交林 (98° - 94°E)→灌丛草甸 (94° -92°E)→草原 (92°- 80°E) ;全新世晚期 (3.2kaBP以后 )由东向西古植被依次为硬叶阔叶林→针阔混交林→草甸→草原→荒漠。     

陇中黄土高原末次冰盛期以来的植被演替及其气候响应

末次冰盛期以来,地球系统经历了一次从冷到暖完整的气候旋回,是过去全球变化研究的一个重要时段。本文基于陇中黄土高原会宁硝沟剖面河湖相-水下黄土沉积序列的高分辨率地层孢粉记录,探讨该区末次冰盛期以来的植被演替及其气候响应模式,旨在为黄土高原生态环境建设的战略部署提供科学依据,且对进一步探讨区域气候演化机制、预测未来气候环境变化趋势具有重要意义。硝沟剖面的孢粉记录揭示,末次冰盛期以来该区的植被演替过程为:荒漠草原(寒冷的盛冰期)→针叶疏林/森林草原(逐渐增温的冰消期)→针阔叶混交林为主的森林草原→针阔叶混交林(温暖的盛间冰期)→针叶疏林草原→干草原/荒漠草原;相应的气候变化模式为:冷干→较温湿→较暖湿→暖湿→温凉偏干→较冷干。总体来看,末次冰盛期以来,研究区植被对气候环境变化的响应非常敏感,随着气候的冷暖干湿变化,森林/疏林草原带自东南-西北发生多次进退;区域顶极植物群落为中全新世气候最适宜期发育的针阔叶混交林,研究区早中全新世较长时期都有较大面积的针阔叶混交林发育;晚全新世植被退化为干草原/荒漠草原,一方面可能是气候持续变干的自然响应,另一方面可能也与此时强烈的人类活动对自然森林/草原植被的破坏导致的恶性循环有关。     

东北地区植被物候期遥感模拟与变化规律

使用1982—2003年GIMMS-NDVI数据,借助GIS空间分析功能,提取东北地区不同植被NDVI时间序列数据,使用分段式Logistic函数模拟了东北地区不同植被物候期,分析了1982—2003年不同植被物候期的变化趋势。结果表明:针叶林、阔叶林、草丛、草甸和沼泽植被生长季开始日期提前,生长季延长,其中沼泽植被生长季开始日期提前和生长季延长的趋势明显,针叶林次之;结束日期的变化趋势表现不一,针叶林和沼泽植被生长季结束日期推迟,阔叶林、草丛和草甸植被呈现微弱提前趋势;针阔混交林、灌丛、草原和农田植被生长季开始日期推迟,生长季缩短,其中农田植被生长季开始日期推迟和生长季缩短的趋势明显,草原次之;针阔混交林、灌丛、草原和农田4种植被生长季结束日期呈现提前的变化趋势,其中灌丛结束日期的提前趋势明显。     

浙江省生态公益林植被恢复过程中物种组成及多样性的变化

在浙江省生态公益林区域的现状植被中分析了6种主要群落类型的物种组成和多样性的变化格局,包括演替系列中的2种灌丛、松优势林、2种混交林和常绿阔叶林。结果表明含松较多的灌丛和松优势林常分布在环境退化较严重(土层瘠薄)的生境中,其中灌木层主要由阳性的映山红、木、白栎等组成,常绿阔叶林优势种木荷、青冈、苦槠、甜槠等在其中偶见,因此推断其自然恢复为常绿林的速度慢;含常绿阔叶树较多的灌丛及含松较少的混交林分布在土层较厚处,木荷、青冈、苦槠、甜槠等的频度和重要值都较大,较容易自然恢复为常绿阔叶林。各种群落中物种多样性指数——Gleason、Shannon-Wiener、Simpson指数基本上以常绿阔叶林为最高,其次是含松较少的混交林,含松较多的灌丛和松优势林各种多样性指数最低。本研究显示我国中亚热带东部森林植被恢复途径有3条:(1)灌草丛→针叶林(松)→针(松)阔混交林→常绿阔叶林;(2)灌草丛→针(松)阔混交林→常绿阔叶林;(3)灌草丛→常绿阔叶林。这意味着本区域的常绿阔叶林恢复可以不必经历松林阶段,在生境条件较好的地方通过人工干预、补种常绿阔叶树可以加速常绿阔叶林恢复。     

河北小五台山主要植被类型的分布与地形的关系：基于遥感信息的分析

小五台山是河北省最高峰,具有较完整的暖温带植被垂直带谱。本文通过野外群落植被调查,结合由TM遥感影像解译1：50000地形图制作的DEM数据而得到的植被图,分析了小五台山主要植被群落的分布状况及其与地形的关系。结果表明,小五台山从低海拔到高海拔,依次出现灌丛、阔叶林、针阔混交林、暗针叶林、矮林、灌丛、草甸等植被类型。森林景观的面积最大,占总面积的60．7％;平均斑块面积最大的是阔叶林和亚高山草甸,斑块破碎化最严重的是水体和针阔混交林。不同的植被类型在不同的地形条件下分布特点不同,林地在北坡所占面积比例(占总面积的75％)远大于南坡(46%),说明水分条件是小五台山森林分布的限制因子之一;灌丛和草甸与林地相反。随海拔高度的变化,不同植被类型的分布面积比例发生变化,出现替代现象,形成植被垂直带谱。由于坡度的影响,增加了带谱内植被组成的复杂性。     

藏北高原典型植被样区物候变化及其对气候变化的响应

植被物候作为陆地生态系统对气候变化的响应和反馈的重要指示,已成为区域或全球生态环境领域研究的热点。基于非对称高斯拟合方法重建了2001—2010年MODIS EVI时间序列影像,利用动态阈值法提取藏北高原植被覆盖2001—2010年每年关键物候参数。选取研究区内东部高寒灌丛草甸、中部高寒草甸及西部高寒草原和高寒荒漠4种典型植被类型,并结合附近的4个气象台站气候资料,分析典型植被物候在近10a对关键气候因子的响应特征。研究结果表明:(1)4种不同典型植被的物候特征(EVImax降低、返青期延后和生长季长度缩短)均表现出高寒灌丛草甸→高寒草甸→高寒草原→高寒荒漠草原的过渡;(2)藏北高原近10a的年平均气温及春、夏、冬三个季度的平均气温均呈显著升高的趋势,升温幅度在0.8—3.9℃/10a,降水减少趋势不显著,在这种水热条件下典型植被均表现出返青提前(7.2—15.5d/10a)、生长季延长(8.4—19.2d/10a)的趋势,而枯黄出现时间为年际间自然波动;(3)高寒灌丛草甸EVImax主要受春季降水量和气温影响,且降水的影响程度大于气温;对高寒草甸植被而言,春、夏季的气温和降水均有较大的影响;而高寒草原和高寒荒漠草原主要受夏季平均气温和降水量影响;(4)高寒灌丛草甸的返青时间主要受前一年秋季降水量的影响,相关系数达-0.579;而高寒草甸、高寒草原和高寒荒漠草原主要受春季平均气温影响,高寒荒漠草原的特征最为明显(r=-0.559)。     

末次冰期以来湛江湖光岩玛珥湖孢粉记录及古环境变化

通过对湛江湖光岩玛珥湖钻孔孢粉记录的研究认为,末次冰期以来,该区植被类型从早期的南亚热带季风常绿阔叶林依次演替为,中亚热带常绿、落叶阔叶林→南亚热带季风常绿阔叶林→中亚热带常绿—落叶阔叶—针叶混交林(湖边草地)→热带季雨林→半常绿季雨林。气候最寒冷的时期温度比目前至少降低了4—6℃以上。全新世早期相对于旱。     

青藏高原全新世花粉记录

全新世青藏高原的花粉记录,反映高原东南部和西北部截然不同的孢粉类型。东南部主要国常绿硬叶种类及潮湿亚热带成分。而西北部几乎没有乔木树种花粉,主要为干旱灌丛和草原成分。文中根据青藏高原２０个湖沼孢粉资料,探讨了青藏高原全新世不同时段、不同地区的植被史及古气候状况。由于高原的特殊大气环流形势,夏半年受西南季风控制,由东南向西北,水份逐渐减弱;冬半年高原面受干冷西风环流影响,致使气候寒冷干燥。全新世植被     

从生态地理特征论中国东北样带(NECT)在全球变化研究中的科学意义

中国东北样带(NECT)是国际地圈生物圈计划(IGBP)全球变化研究的陆地样带之一。该样带在东经112°与130°30′之间沿北纬43°30′设置,长约1600km,跨越北纬42°～46°,宽约300km,位于中纬度温带地区以降水或湿润度/干燥度为主要全球变化驱动因素,自东至西沿一个连续的空间过渡梯度,植被类型或生物群区是由温带针阔叶混交林、温带落叶阔叶林、农田及温带草原的3个亚地带:草甸草原、典型草原和荒漠草原等类型组成。给出了样带的基本生态地理特征及其梯度分析,包括其地理位置、地形地貌、气候梯度、土壤类型、土地利用格局、植被类型、主要优势种和群落类型的生态地理特征以及全新世适宜期的植被分布格局。这些特征沿经向均表现出明显的梯度分布。     

腾格里沙漠晚更新世孢粉植物群与气候环境演变

根据腾格里沙漠断头梁人工开挖剖面距今约４２０００～２３０００ａＢＰ（晚更新世）的孢粉分析结果,可将该期植被和气候演化划分为５个阶段（组合带）：阶段Ⅰ,约４２０００～３８０００ａＢＰ,此段孢粉组合特征显示出,在现今为戈壁荒漠的山地丘陵上,当时发育着针阔混交林,在古湖边缘上发育着杨柳林和草原,气候较温暖湿润;阶段Ⅱ,约３８０００～３１０００ａＢＰ,气候温暖湿润,地带性植被为以温带、暖温带阔叶林为主的针阔混交林,湖畔河边发育着草甸植被;阶段Ⅲ,约３１０００～３００００ａＢＰ,为针叶林和寒温性高山柳丛大发展时期,气候寒温,为一冷期;阶段Ⅳ,约３００００～２８０００ａＢＰ,为冷期过后的升温期,也是湖面扩大期,孢粉组合中藻类含量高,为草甸和沼泽植被;阶段Ⅴ,２８０００～２３０００ａＢＰ,孢粉组合显示出丘陵山地上发育温带柏和桦为主的针阔混交林,平原上生长着草原植被,湖畔、河边有柳林分布,气候较温暖湿润,但较阶段Ⅰ略干。此剖面孢粉组合所反映的气候变化特征与古里雅及格陵兰冰芯δ１８Ｏ所记录的同期气候变化特征具有良好的可比性。     

Palynoflora at Late Miocene?aEarly Pliocene from Leijiahe of Lingtai,Gansu Province,China

Vegetation and climate changes of Late Miocene-Early Pliocene have been deduced based on pollen research from Wenwanggou and Xiaoshigou sections near Leijiahe village (ca 35°04′15″N,107°43′30″E). The two sections are quite famous of rich micromammalian fossils. Before ca. 6.5 Ma, open forest-grassland was distributed in the studied area indicating a temperate and humid condition at that time. In the period between ca.6.5 and 5.8 Ma BP (Late Miocene) predominance of Chenopodiaceae and Artemisia implies that desert or desert-grassland was developed in the area and the climate should be cold and dry. During the time interval from ca.5.8 to 3.4 Ma BP mixed conifer and broad leaved deciduous forest with a few subtropical tree taxa had replaced the arid desert vegetation indicating a warm and humid climate. The climate aridity event of Late Miocene can be correlated with the global climatic event.     

Vegetation History of the Southern Loess Plateau of China During the Last 100000 Years Based on Pollen Data

The paper deals with the vegetation history of the southern Loess Plateau, central China, for the last 100 ka based on palynological records from Weinan section. The pollen diagram of the loess-paleosol sequence at Weinan, southern part of the Plateau (109~30rE, 34°24′N), displays a predominence of arid shrubs or herbs (Arternisia, Chenopodiaceae) alternating with the abundance of mesic herbs (Cyperaceae, Ranuculaceae, Liliaceae etc. ) indicating a succession of steppe and meadow-steppe in turn during the last 100 ka BP. Forest vegetation developed only in some comparatively short time intervals e. g. Ulmus forest at ca. 95.1～90.0 ka BP (9. 50～9.32 m); Corylus woodland at ca. 25.0～21.1 ka BP (4.00～3.48 m) and Tsuga stand at ca. 13.7～11.8 ka BP (2.20～1.80 m). So far plant ecologists assinged the southern Loess Plateau to temperate broadleaf deciduous forest zone. Actually there are no forests on. the Plateau surfaces today. The lack of forest from the Plateau surface today is explained as being due to human interferences by plant ecologists. However, in the context of the last 100 ka BP it seems that there has been some nonhuman factors responsible for the treelessness of the Plateau, such as the free-draining nature of loess, which deserves greater consideration.     

Vegetation and Climate Change during the Last Deglaciation in the Great Khingan Mountain,Northeastern China

The Great Khingan Mountain range, Northeast China, is located on the northern limit of modern East Asian Summer Monsoon (EASM) and thus highly sensitive to the extension of the EASM from glacial to interglacial modes. Here, we present a high-resolution pollen record covering the last glacial maximum and the early Holocene from a closed crater Lake Moon to reconstruct vegetation history during the glacial-interglacial transition and thus register the evolution of the EASM during the last deglaciation. The vegetation history has gone through distinct changes from subalpine meadow in the last glacial maximum to dry steppe dominated by Artemisia from 20.3 to 17.4 ka BP, subalpine meadow dominated by Cyperaceae and Artemisia between 17.4 and 14.4 ka BP, and forest steppe dominated by Betula and Artemisia after 14.4 ka BP. The pollen-based temperature index demonstrates a gradual warming trend started at around 20.3 ka BP with interruptions of several brief events. Two cold conditions occurred around at 17.2–16.6 ka BP and 12.8–11.8 ka BP, temporally correlating to the Henrich 1 and the Younger Dryas events respectively, 1and abrupt warming events occurred around at 14.4 ka BP and 11.8 ka BP, probably relevant to the beginning of the Bølling-Allerød stages and the Holocene. The pollen-based moisture proxy shows distinct drought condition during the last glacial maximum (20.3–18.0 ka BP) and the Younger Dryas. The climate history based on pollen record of Lake Moon suggests that the regional temperature variability was coherent with the classical climate in the North Atlantic, implying the dominance of the high latitude processes on the EASM evolution from the Last Glacial Maximum (LGM) to early Holocene. The local humidity variability was influenced by the EASM limitedly before the Bølling-Allerød warming, which is mainly controlled by the summer rainfall due to the EASM front covering the Northeast China after that.     

暖温带山地森林的小气候研究

本文探讨了暖温带山地落叶阔叶混交林和油松林不同梯度的气温、湿度、土壤温度的日变化特征,不同季节的分析结果表明：１．落叶阔叶林夜间始终存在气温随高度增加而增加（第１梯度＞第２梯度＞第３梯度＞第４梯度）的辐射逆温现象。油松林夜间林内气温观测值始终低于林冠以上值。２．在生长季的不同时期,人工油松林的林内气温（林地以上２ｍ和４ｍ）的日间波动程度和振幅都高于林冠以上（林冠顶以上０．５ｍ和２．５ｍ）。而在生长季中期,充分发育的落叶阔叶林林冠能够明显地缓减林内气温波动和振幅。３．两类林分各梯度的气温一般均在正午后２～３小时内达到高峰,而早晚较低,具有明显的日变化特征。４．落叶阔叶林林冠以上２．５ｍ处的水汽压及相对湿度始终低于林地以上４ｍ（林下灌木层以上２．５ｍ）处的同期值,具有比油松林更强的增湿效应。     

中国东部森林植被带划分之我见

简要回顾了中国东部森林植被带划分研究的历史及当前存在的争论。提出了中国东部植被带划分应以植被本身的特征，特别是地带性的生物群落集为主要依据，同时参照它们的区系组成和气候指标。根据上述原则将中国东部划分为６个植被带∶北方针叶林带、凉温带针阔混交林带、温带落叶阔叶林带、暖温带常绿落叶阔叶混交林带、亚热带常绿阔叶林带和热带雨林、季雨林带，并对各植被带的特征作了简要的描述。阐述了对一些植被带名称、界线改动的原因，特别讨论了我国常绿落叶阔叶混交林以及常绿阔叶林生物气候带的归属问题，认为前者归属于暖温带植被，后者归属于亚热带植被为宜。     

用数值分类系统探讨浙江九龙山植被类型的划分

 九龙山位于浙江省遂昌县西南部,北纬28˚21′,东经118˚52′。土地面积约75km2。主峰海拔1724m。植物种类丰富,初步统计约有种子植物143科、584属、1149种。植物区系起源古老,地理成分以热带、亚热带成分组成为主。本文用数值分类NTS专用软件在IBM—PC型计算机进行数值分类。主要有6个植被型：常绿阔叶林,常绿、落叶阔叶混交林,落叶阔叶林,山顶矮林,针叶林和竹林。常绿阔叶林为本区地带性植被,常绿、落叶阔叶混交林为本区主要的植被类型。     

青藏高原东南部18ka以来气候与水文变化

青藏高原东南部众多封闭小湖的湖相沉积记录着重要的地理信息,是恢复当地晚更民以来古环境演变的理想材料。西藏海登湖和仁同分辨率的花粉组合,ＡＭＳ＾１４Ｃ测年及磁化率和有机质含量测定,揭示了研究区与鳊季风密切相关的古植被,古气候和古水文变化历史。高分辨率的花粉记录反映,在１６ｋａＢｍ,Ｐ,以前花粉组合以黎科（Ｃｈｅｎｏｐｏｄｉａｃｅａｅ）和蒿属（Ａｒｔｅｍｉｓｉａ）为主,花粉浓度很低,应为荒漠草原植被。     

再论中国植被分区的原则和方案

 本文首先提出中国植被分区的原则和依据以及高级分区单位的标志,将全国划分为八大植被区,其中有五个区包括两个亚区,因作者主张亚区与区作为同一级的辅助单位看待,所以实际上把全国分为13个高级植被分区单位。除少数例外,每一植被区或亚区都分为一过渡带和典型带。全文以植被区或亚区、植被地带或亚地带为单位,论述其植被特点。     

山东植物区系的演变和来源

1　现代植物区系山东省位于我国东部、黄河下游 ,北濒渤海 ,东临黄海 ,地理范围介于北纬 34°2 3′～38°2 4′,东经 1 1 4°4 8′～ 1 2 2°4 3′之间。全省总面积为 1 5.72万 km2 ,占全国总面积的 1 .6%。属暖温带季风气候 ,沿海比较湿润 ,地带性植被主要是暖温带落叶阔叶林和松、栎类针阔叶混交林。山东省在中国植物区系的分区地位隶属于泛北极植物区、中国 -日本森林植物亚区、华北植物地区 [1 ]。据最近研究统计 ,现有野生维管植物 1 47科、61 4属 ,约 1 547种 (包括变种 ,下同 )。其中蕨类植物 2 4科 39属 1 0 5种 ,裸子植物 3科 3属 …     

An Ecogeographical Regionalization for Biodiversity in China

Ecogeographical regionalization is the basis for spatial differentiation of biodiversity research. In view of the principle of international ecogeographical regionalization, this study has applied multivariate analysis and GIS method and based on some ecogeographical attributes limited to the distribution of plant and vegetation, including climatic factors, such as minimum temperature, mean temperature of the coldest month, mean temperature of the wannest month, annual average temperature, precipitation of the coldest month, precipitation of the wannest month, annual precipitation, CV of annual precipitation, biological factors such as vegetation types, vegetation division types, NPP, fiorisitic types, fauna types, abundance of plant species, genus and endemic genus; soil factors such as soil types, soil pH;topographical factors as longitude, latitude and altitude etc. The ecogeographical regionalization for biodiversity in China was made synthetically by using fuzzy cluster method. Four classes of division were used, viz., biodomain, subbiodomain, biome and bioregion. Five biodomains, seven subbiodomains and eighteen biomes were divided in China as follows: Ⅰ Boreal forest biodomain. Ⅰ A Eurasian boreal forest subbiodomain. Ⅰ A1 Southern Taiga mountain cold-temperate coniferous forest biome; Ⅰ A2 North Asian mixed coniferous-broad-leaved forest biome. Ⅱ Northern steppe and desert biodomain. Ⅱ B Eurasian steppe subbiodomain. Ⅱ BI Inner Asian temperate grass steppe biome; Ⅱ B2 Loess Plateau warm-temperate forest/shmb steppe biome. Ⅱ C Asia-Mrica desert subbiodomain. Ⅱ C1 Mid-Asian temperate desert biome; Ⅱ C2 Mongolian/Inner Asian temperate desert biome. Ⅲ East Asian biodomain. Ⅲ D East Asian deciduous broad-leaved forest subbiodomain. Ⅲ D1 East Asian deciduous broad-leaved forest biome, Ⅲ E East Asian evergreen broad-leaved forest subbiodomain. Ⅲ El East Asian mixed deciduous-evergreen broad-leaved forest biome; Ⅲ E2 East Asian evergreen broad-leaved forest biome; Ⅲ E3 East Asian monsoon evergreen broad-leaved forest biome; Ⅲ FA Western East Asian mountain evergreen broadleaved forest biome. Ⅳ Palaeotropical subdomain. IV F India-Malaysian tropical forest subbiodomain.Ⅳ Fl Northern tropical rain forest/seasonal rain forest biome; Ⅳ F2 Tropical island coral reef vegetation biome. Ⅴ Asian plateau biodomain. Ⅴ G Tibet Plateau subbiodomain. Ⅴ G1 Tibet alpine highcold shrub meadow biome;Ⅴ G2 Tibet alpine high-cold steppe biome; Ⅴ G3 Tibet alpine high-cold desert biome; Ⅴ G4 Tibet alpine temperate steppe biome; Ⅴ G5 Tibet alpine temperate desert biome.