9 resultados para Forest structure
em Chinese Academy of Sciences Institutional Repositories Grid Portal
Resumo:
长白山自然保护区始建于1960年,位于北坡的红松针阔叶混交林森林生态系统是我国东北地区典型温带地带性森林植被之一,面临着全球气候变化和人类干扰的双重影响。 本研究以间隔43年的野外调查数据为基础,对1963年和2006年的长白山自然保护区北坡海拔800~1700m的森林植物群落进行对比分析,得到该区域的森林结构、植物多样性与碳储量的变化特点,讨论森林动态变化与人类活动、气候变化的关系,评价长白山自然保护区的保护效果: 对长白山北坡森林沿海拔梯度的森林结构和植物多样性的分析表明:群落的整体空间格局保存完好,植物种类变化不大,乔木层的建群种的种类基本不变,植物多样性与海拔高度呈负相关关系;林下层植物多样性受小环境影响,与海拔高度无明显相关。 以红松(Pinus koraiensis)针阔混交林、红松针叶混交林和云冷杉暗针叶林三种类型为单元分别研究各森林类型的多样性变化:α多样测度选择物种丰富度、Shannon-Wiener和Pielou均匀度指数,较好体现了样地内发生的多样性变化,灌木层和草本层多样性明显下降,一些稀有种和药用物种消失,红松等原优势物种有衰退趋势,阔叶树比例增大;β多样性测度选取Cody指数,体现出海拔梯度上的植被空间格局细节变化,演替层特别是阔叶树的物种更替变化有向高海拔移动的趋势。 对森林生态系统各层次碳储量进行估算:乔木层和灌木层采用维量法,对灌木层自建生长回归方程;草本层、枯枝落叶层采取收获法;植物细根采取根钻法;土壤采取土壤深度加权法。碳密度估算结果都与前人研究结果相似。各类型植被碳库总碳密度都达到170 t/hm2,远远高于国内平均森林植被碳库密度值44.9 t/hm2。 乔木层43年来的碳储量变化都无显著性差异,但仍表现出:阔叶树种碳储量上升,特别在高海拔类型这种变化更加明显;针叶树种碳储量在暗针叶林内大幅下降;树干的碳库分配比例都有所减少,表明植被碳库正存在向不稳定性方向发展的趋势。针阔混交林和暗针叶林的土壤碳储量,与植被碳库出现相反的变化趋势,整体碳库保持在一个相对平衡的状态。 推测造成这种变化的原因是:禁止砍伐等保护措施的实施,基本保存了乔木层垂直分布格局,而气候变暖使阔叶树种比例大幅增加,采集松籽等人类生产及旅游活动对林下层植被影响破坏较大。提议加强保护区内管理力度和规划,以减缓长白山北坡森林群落的不稳定变化趋势。
Resumo:
以沈阳市城区与环城区为对象借助于航片和卫片利用GIS进行城市森林结构的研究。针城市森林的性质和特点,以大功能为主体,结合植被类型,确定城市森林的4级分类单位,结合我国城市森林现状和分类原则,将城市森林分为五大类,并将沈阳城市森林分为5个城市森林类,16个城市森林亚类,43个城市森林组以及181个城市森林型。研究表明,沈阳城区乔木总体上胸径偏小,树高偏低,缺少大树,总体健康状况有待于提高,树种过于集中,主要乔木树种为杨柳榆(刺)槐以及油松和圆柏6种,其他树种占据比重较小,灌木生长良好。环城区乔木状况与城区相似,各状况更差,主要乔木树种为油松、蒙古栋和刺槐。城区森林覆盖率为7.15%,三维绿量总量为1.61E+08m3,总叶面积为1.13E+08m2,环城区森林覆盖率为4.82%,中心城区三维绿量和总叶面积分别为1.76E+08m2和1.51E+O8m2,环城区分别为4.44E十08m3和3.82E+08m2。获得主要树种的三维绿量模拟方程。沈阳城市森林总体景观格局分布均匀,但破碎化程度较大,大斑块分布不均匀,景观美学价值普遍较低。通过对所调查的样地进行综合评价并排序,获得沈阳市城市森林结构最优化类型,并对城市森林发展提出建议。
Resumo:
本文系统研究了沈阳城市森林的布局与结构、城市森林功能、城市森林病虫害发生与树木健康状况和城市自然资源与社会经济状况等指标对沈阳城市森林生态系统健康与管理的影响。同时一,采用2种生态系统健康评价方法对沈阳城市森林生态系统健康状况进行了评价,并提出了沈阳城市森林生态系统健康管理的对策。研究结果如下:1、截至2004年末,沈阳城市森林植被覆盖率已经达到35%,城市森林林地分布基本合理,但需要进一步加强道路林地、居住区林地和城郊大面积生态林建设。2、沈阳城市森林以乔木为主,乔灌株数比为1.7:1,乔灌的覆盖度比约为7:1。3、沈阳城市森林不同类型林地中植物组成不同。公园林地中有74个属,137个种(变种);庭院林地中有53个属,104个种(变种);居住区林地中有45个属,81个种(变种);道路林地中有43个属,94个种(变种);运河风景林地中有75个属,142个种(变种);棋盘山风景林地中有48个属,118个种(变种)。4、公园林地、庭院林地、居住区林地、道路林地和运河风景林地的Shannon一Wiener多样性指数分别为2.78、3.05、3.15、3.18和3.18,均匀度指数分别为0.56、0.66、0.72、0.70和0.64。除了棋盘山风景林地外,沈阳城市森林中栽植总量超过乔木总量5%的乔木树种有7个属,分别为李、柳树、杨树、桧柏、榆树、槐树和银杏,7种树木总量达到了全部乔木总量的82.09%;栽植总量超过灌木总量5%的灌木树种也有7个属,分别为水腊、丁香、李属,小聚、玫瑰、忍冬和连翘,7个属灌木总量达到了全部灌木总量的87.92%。5、公园林地、庭院林地、道路林地和防护林地中OBH<20cm、20cm<DBH<60cm和DBH>60cm树木的比例分别为:57.9%、40.0%、2.1%,49.2%、47.8%、3.0%,65.3%、33.1%、1.6%和64.6%、34.9%、0.5%,表明沈阳城市森林树木的规格总体上偏小。6、经样方调查和CITYgreen模型计算,沈阳城市森林的生态效益约2.0亿USD/yr.。公园林地、庭院林地和风景林地的景观指标相对较高;道路林地和居住区林地的景观效果一般;防护林地的景观效果较差。7、目前已经发现的沈阳城市森林病害约600余种,虫害约700余种,其中杨树主要病虫害39种,柳树的主要病虫害有33种,榆树和槐树的主要病虫害均为,1种。杨柳树腐烂病、光肩星天牛、天幕毛虫、桃红颈天牛和美国白蛾等是近10年来沈阳城市森林中普遍发生和造成严重危害的主要病虫害。沈阳城市森林主要树木的平均健康指数为2.68,处于一般健康状态。8、沈阳城市森林的土壤和水资源状况均不利于树木的健康生长,沈阳的社会经济发展也有待于进一步提高。9、经过生物指示物法(光肩星天牛为生物指示物)、专家权重法、公众问卷调查和对比研究,沈阳城市森林生态系统总体上处于亚健康状态。10、通过对沈阳城市森林资源、管理状况的调查研究和健康状况的评价,本文提出了沈阳城市森林生态系统健康管理的对策,包括合理规划沈阳城市森林林地布局,增加道路林地、居住区林地和城郊林地的面积和植被覆盖率;调整树木种类组成,避免单一或少数树种的大量栽植,提高生物多样性水平;保护大树和古树;增加城市森林管理资金的投入;应用先进技术,采取科学的病虫害防治和植物养护方法,促进树木的健康生长等。This project systematically studied the urban forest ecosystem health and management in Shenyang. The study explored factors, such as urban forest structure, distribution, pests, aesthetic value, ecological benefit, natural resources and socieo-economic status, that affecting the urban forest ecosystem health and management. Two methods were used to evaluate the ecosystem health. This project also proposed Shenyang's urban forest ecosystem health management strategies. The research results can be summarized as follows: 1. As of the end of 2004, urban forest coverage in Shenyang is about 35%, and is in relatively even patch distribution pattern. However, the street trees and roadside forest patches, residential block forest patches should be enhanced. 2. Trees are the major component of the Shenyang s urban forest, followed by shrubs. The quantity ratio of tree to shrub is about 1.7:1, and the coverage ratio of trees to shrub is about 7:1. 3. Species composition varies by location. There are 74 genera, 137 species (including varieties) in the public parks; 53 genera, 104 species (and var.) in the green spaces of the institution (including school), factory, and company; 45 genera, 81 species (var.) in residential blocks; 43 genera, 94 species (var.) in streets and roadside forest patches; 75 genera, 142 species (var.) in the Canal landscape forest patches; 48 genera, 118 species (var.) in the Qipan Mountain recreation forest. 4. The Shannon-Woener indices varies in parks, in institution, factory, and company yards, in streets and roadside forest patches, in residential blocks.there are 2.78, 3.05, 3.18, 3.15, 3.18, respectively; and the evenness indices are 0.56, 0.66, 0.70, 0.72, 0.64, respectively. Besides the Qipan Mountain forest patches, trees of 7 genera, Prunus spp., Salix spp., Populus spp., Sabina spp., Ulmus spp., Robinia spp. and Ginkgo biloba are of more than 5% the total urban trees, respectively. In fact, trees from these 7 genera are about 82% of all trees in Shenyang's urban forests. In terms of shrubs, species of 7 genera, Ligustrum spp., Syringa spp., Prunus spp., Berberis spp., Rosa spp., Lonicera spp., and Forsythia spp. are more than 5% the total urban shrubs, respectively. 88% of all the shrubs in Shenyang s urban forest are from these 7 genera. 5. The diameter class of DBH<20cm, 20cm
Resumo:
Figs (Moraceae) and their pollinating wasps (Agaonidae) constitute a famous reciprocal mutualism in which figs provide some female flowers for the development of fig wasp offspring while the fig wasps pollinate Fig flowers. However, figs also host many no
Resumo:
How coniferous trees in northern China changed their distribution ranges in response to Quaternary climatic oscillations remains largely unknown. Here we report a study of the phylogeography of Pinus tabulaeformis, an endemic and dominant species of coniferous forest in northern China. We examined sequence variation of maternally inherited, seed-dispersed mitochondrial DNA (mtDNA) (nad5 intron 1 and nad4/3-4) and paternally inherited, pollen- and seed-dispersed chloroplast DNA (cpDNA) (rpl16 and trnS-trnG) within and among 30 natural populations across the entire range of the species. Six mitotypes and five chlorotypes were recovered among 291 trees surveyed. Population divergence was high for mtDNA variation (G(ST) = 0.738, N-ST = 0.771) indicating low levels of seed-based gene flow and significant phylogeographical structure (N-ST > G(ST), P < 0.05). The spatial distribution of mitotypes suggests that five distinct population groups exist in the species: one in the west comprising seven populations, a second with a north-central distribution comprising 15 populations, a third with a southern and easterly distribution comprising five populations, a fourth comprising one central and one western population, and a fifth comprising a single population located in the north-central part of the species' range. Each group apart from the fourth group is characterized by a distinct mitotype, with other mitotypes, if present, occurring at low frequency. It is suggested, therefore, that most members of each group apart from Group 4 are derived from ancestors that occupied different isolated refugia in a previous period of range fragmentation of the species, possibly at the time of the Last Glacial Maximum. Possible locations for these refugia are suggested. A comparison of mitotype diversity between northern and southern subgroups within the north-central group of populations (Group 2) showed much greater uniformity in the northern part of the range both within and between populations. This could indicate a northward migration of the species from a southern refugium in this region during the postglacial period, although alternative explanations cannot be ruled out. Two chlorotypes were distributed across the geographical range of the species, resulting in lower levels of among-population chlorotype variation. The geographical pattern of variation for all five chlorotypes provided some indication of the species surviving past glaciations in more than one refugium, although differentiation was much less marked, presumably due to the greater dispersal of cpDNA via pollen.