首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献,搜索用时 58 毫秒
1.
孙然好  程先  陈利顶 《生态学报》2017,37(24):8445-8455
水生态功能分区是针对水生态系统特征的陆地生态系统划分,是为流域水生态管理提供生态背景和基本单元。陆地-水生态系统的耦合是水生态功能分区的核心,但多停留在个别小流域进行理论探讨,大型流域的实际案例较少。针对海河流域独特的气候、地貌、水文和人类活动特征,提出了水生态功能分区的三级指标体系。一级二级区针对气候、地貌、水文背景进行"自上而下"的分区,三级区针对人类活动对水资源、水环境、生境影响,采用"自下而上"的分区方法。最终,海河流域划分了6个一级区、16个二级区和73个三级区。研究充分体现了"以水定陆、以陆控水"的基本原则,以及"自下而上"和"自上而下"分区方法的优点,结果可为海河流域水生态管理提供科学依据,为水资源空间调配与合理利用、产业结构布局与区域协调等服务。  相似文献   

2.
基于遥感和GIS的巢湖流域生态功能分区研究   总被引:4,自引:0,他引:4  
生态功能分区是区域自然资源科学管理及可持续发展利用的基础。基于生态功能分区原则,考虑流域——子流域完整性进行巢湖流域生态功能分区。在综合分析巢湖流域生态环境基本特征的基础上,确定生态功能分区原则、依据、方法及命名,基于遥感与GIS在数据采集方面及多层面叠加功能的优势,通过遥感数据对研究区土地利用信息的提取以及利用DEM空间分析进行子流域划分等技术手段,探讨了遥感和GIS技术支持下的研究区子流域生态功能划分方法,形成了巢湖流域生态功能分区方案,将全流域分为5个生态功能区和12个生态功能亚区,并阐明了不同生态功能区的生态保护重点与经济社会发展约束。对于新调整行政区划的巢湖流域生态环境综合治理具有重要的现实意义,可为流域产业布局、生态防灾减灾、环境保护与建设规划等提供科学依据。  相似文献   

3.
水生态一、二级分区技术框架   总被引:8,自引:1,他引:7  
刘星才  徐宗学  徐琛 《生态学报》2010,30(17):4804-4814
水生态功能分区是流域水环境分类、分级、分区、分期管理的基础。回顾总结国内外水生态功能分区工作的基础上,针对我国流域水生态功能一、二级分区工作,提出了一个可供参考的分区指标体系,探讨了流域尺度水生态分区技术框架的构建以及可能存在的问题。该技术框架主要由3部分内容组成:环境要素对水生态因子的驱动机制、分区指标体系和分区技术。作为技术框架的理论依据,驱动机制分析首先以水-陆生态水文耦合模型为框架对环境要素如何影响水生态系统功能进行阐述。指标体系是技术框架的基础部分,主要包括水生态因子和环境要素两大类,其中一级分区指标包括气候、水文和地貌等要素,二级分区指标包括水质、水生动植物、藻类、土壤、植被、土地利用和社会经济要素。针对一、二级水生态功能区采用"自上而下"和"自下而上"的分区方法,为技术框架付诸现实提供了保障。为正在进行的各大流域水生态功能分区工作提供一定的参考依据,同时也希望在这些具体分区工作的基础上能进一步完善本分区技术框架。  相似文献   

4.
洱海流域水生态分区   总被引:4,自引:0,他引:4  
分区边界的确定是生态分区的重要步骤,但目前多数水生态分区的边界确定以定性分析、专家判断为主。本研究以洱海流域为例,建立了一套两级分区体系。该体系基于GIS技术,用子流域作为分区基本单元,并用相关分析法,定量筛选一、二级分区指标。其中,一级分区指标为高程、坡度和植被归一化指数(NDVI),二级分区指标为农田百分比和城镇百分比。通过指标图层的叠加和重分类,合并同质性子流域,从而将洱海流域划分为5个一级区和9个二级区。藻类群落分布的验证结果表明分区合理。本研究将定量分析和子流域边界应用于水生态分区,使分区边界的确定更科学,在实际管理中更具有可操作性。本研究结果为水生态分区研究提供了新的方法,为洱海流域水生态管理提供了基本管理单元。  相似文献   

5.
李翔  张远  孔维静  郦威  卫毅梅  冯祯 《生态科学》2013,32(6):744-751
流域水生态功能区是管理流域水生态系统的基本单元,其特点是统筹陆地和河流生态系统,更好、更全面反应流域水生态系统的整体特征。通过对流域内重要生境的识别,可以为区域内生物保护目标、生态安全目标、流域管理等方案的制定和实施提供重要的科学依据。该文以辽河保护区为例,从分区理论、划分方法、指标体系建立和划分结果四个方面详细介绍了分区过程,最终以保护区内主要自然影响和人类干扰作为主要分区指标,将辽河保护区划分为8 个水生态功能三级区,并总结了各功能区的地貌、河段特征和土地利用特征等。研究结果将有助于对辽河保护区的内生态环境状况进行修复与改良。  相似文献   

6.
水生态功能分区的研究进展   总被引:12,自引:1,他引:11  
水生态功能分区是基于对流域水生态系统的区域差异的研究而提出的一种分区方法.它阐明了水生环境系统在区域和地带等不同尺度上的空间分异特征,并揭示出水生态系统空间分布规律.本文系统阐述了水功能区划、水环境功能区划、生态地理分区、生态分区以及水生态功能分区等几个重要分区概念的区划方法、目标及局限性,并综述了国内外水生态功能分区的研究进展,比较了国内外分区框架体系的差异,指出了我国水生态功能区划的缺陷,并对其发展趋势进行了展望.  相似文献   

7.
和克俭  黄晓霞  丁佼  刘琦  江源 《生态学报》2019,39(15):5483-5493
流域水生态功能分区研究是我国正在开展的一项重要工作,如何验证分区结果的合理性,是当前亟待解决的问题。采用地理加权回归(GWR)模型评估流域特征对东江水质的影响,验证水质及流域影响空间差异是否与一二级水生态功能分区结果吻合,并对比了GWR模型与普通最小二乘(OLS)模型性能,讨论了GWR在分区验证方面的应用价值及不足。结果显示:1)水质指标以及GWR模型局部解释率(Local R~2)均在一二级水生态功能分区间存在显著差异;2)相比OLS模型,GWR模型校正R~2更高,残差空间自相关指数Moran′s I更低。研究表明东江水生态功能分区结果能合理反映水陆耦合关系,有效解释水质空间差异。此外建议选择总氮(TN)而非溶解氧(DO)和总磷(TP)作为分区验证指标。GWR模型在分区结果验证中具有广泛应用前景。降低数据空间自相关影响及改善距离测度方法是未来GWR模型研究的难点问题。  相似文献   

8.
水生态功能分区研究中的基本问题   总被引:10,自引:1,他引:9  
唐涛  蔡庆华 《生态学报》2010,30(22):6255-6263
重点流域水生态功能一级二级分区研究是当前我国正在开展的一项重要工作,如何进行科学、合理的分区是值得深入探讨且亟待回答的重要问题。从水生态功能分区与水生态区划的关系、水生生物在分区中的应用、以及如何选取合适的定量分析方法等方面入手,阐述了对分区目的、指标体系和技术方法等关键问题的理解。并建议:(1)统一选用流域水生态系统结构、功能空间差异的环境驱动因子作为分区指标体系;(2)用生境尺度的水环境、水生生物指标来验证分区结果;(3)尽可能统一定量分析方法,以便为不同流域间分区结果的比较,以及为将来在全国尺度上开展分区工作奠定基础。  相似文献   

9.
水生态功能区划流程:双关系树框架与概念模型   总被引:1,自引:0,他引:1  
郭书海  吴波 《生态学杂志》2017,28(12):4051-4056
水生态区划和水生态功能区划是流域水环境管理与水生态系统合理利用的重要基础,国内已经研究十年有余.本文针对该领域的一些共性问题,通过对水生态区划分与水生态功能类型划分的系统分析,探讨了水生态区划与水生态功能区划的关联性,提出了基于双树结构的RFCH流程和钻石概念模型;并以辽河流域为例,参照其他研究者的区划方案,开展了以水生态三级区为基础的水生态功能分类,为流域水生态功能区划提供了一种可借鉴的流程框架.  相似文献   

10.
海河流域生态功能区划   总被引:4,自引:1,他引:3  
从海河流域自身的特征出发,运用RS、GIS技术,采用定性和定量分析相结合的方法,对海河流域生态功能区进行划分.结果表明:海河流域可划分为5个生态区、24个生态亚区和114个生态功能区;以流域尺度上占主导地位的4项生态功能(水源涵养、水土保持、防风固沙和生物多样性保护)为依据,确定了对海河流域具有重要意义的11个重要生态功能区域.该区划结果明确了对海河流域生态安全具有重要意义的区域,可用于指导海河流域自然资源的有序开发利用和产业的合理布局,为海河流域生态环境保护提供了科学依据,对维护海河流域生态安全具有重要意义.  相似文献   

11.
Summary In 1982 and 1983 root samples were taken by auger from potato crops grown on marine clay in the Flevo-Polder. The roots increased their penetration depth throughout the periods of measurement, and ultimately reached depths between 80 cm and 100 cm below the hills. Between 50 and 60 days after emergence, decay of roots commenced, starting in the upper horizons. In the hill mean root length densities varied between 1 and 2 cm cm−3. Below the hills root density rarely exceeded 1 cm cm−3. The random variation in root density was equivalent to a coefficient of variation of 50%. There were significant effects of the position of sampling (relative to the centre of the plant) on root density; densities were usually lowest beneath the furrow. Depending on season and sampling date, total root length varied between 3.4 and 7.1 km m−2, and root dry mass varied between 33 and 77 g m−2. Representative figures for specific root length were 100–120 m g−1 dry weight. About 90% of the root diameters were smaller than 0.44 mm; the most frequent class (35%) were roots with diameters between 0.12 and 0.20 mm.  相似文献   

12.
Summary The soil-block technique was developed to estimate fine root production in forest ecosystems. This technique produced estimates similar to conventional soil coring but required less labor and reduced disturbance to the soil-root environment.  相似文献   

13.
14.
Proliferation of roots in a nutrient patch can occur either as a result of an increase in root length (morphological response) or by a change in root birth or death rates (demographic responses). In this study we attempted to distinguish between these two mechanisms of response to nutrient patches and to compare the responses of four old-field plant species (two annuals, two perennials). For all four species combined, there were significant increases in root numbers and root length in fertilized patches. Root proliferation in fertilized patches was largely due to increased birth (=branching) rates of new roots. However, there was also a significant increase in root death rates in the fertilized patches which reduced the magnitude of the increase in net root numbers. Plots for individual species suggested they differed in the magnitude and timing of root proliferation in fertilized patches due to differences in root birth and death rates. However, because of the limited sample size in this study, there was only a marginally significant difference among species in root birth rates, and no difference in death rates. Further studies are currently underway to better quantify species differences in the demographic mechanism, as well as magnitude, of response to nutrient patches and if this would affect the ability to exploit small-scale heterogeneity in soil resources.  相似文献   

15.
Empirical and theoretical studies have highlighted that plantcompetition and species diversity are substantially affected by interactionsamong plant growth and nutrient uptake rates, root lateral spread, rootplasticity, and small scale soil nutrient heterogeneity. This study wasdesignedto (a) experimentally estimate parameters regarding rootscaling patterns, root biomass allocation, growth rates, nutrient productivity,and root nutrient influx rates of 55 plant species common to Great Plainsgrasslands; and (b) determine if grasses and forbs can beclassified into statistically distinct groups based on these characteristics.Wefound that: (1) In all species root lateral spread, rootlength, and root surface area had significant allometric scaling relationshipswith root biomass, but that the relationships were unaffected by Navailability.(2) Reductions in the supply of N increased the root:shootratio in 62% of the species. (3) The frequency distributionandmean values of maximum relative growth rates were very similar for grasses andforbs/shrubs, but mid successional grasses had a higher relative growth ratethan late successional ones. (4) In 78% of the species tested,N productivity was increased by reductions in the N supply.(5)When subjected to a high N supply, the N and P productivity of grasses was, onaverage, higher than that of forbs/shrubs, and the N and P productivity ofC4 grasses was, on average, higher than that of C3grasses. No differences were found under a low N supply. (6)Nodifferences on the average maximum N and P influx rates per unit of rootsurfacearea were found between grasses and forbs or between C3 andC4 grasses, but both were correlated with maximum relative growthrate. (7) The set of parameters we measured were able toseparate grasses and forbs/shrubs into statistically distinct groups that tendto follow in broad terms the coarse vs. fine scaleforaging strategies hypothesis.  相似文献   

16.
Allen A  Snyder AK  Preuss M  Nielsen EE  Shah DM  Smith TJ 《Planta》2008,227(2):331-339
Plant defensins are small, highly stable, cysteine-rich antimicrobial proteins that are thought to constitute an important component of plant defense against fungal pathogens. There are a number of such defensins expressed in various plant tissues with differing antifungal activity and spectrum. Relatively little is known about the modes of action and biological roles of these proteins. Our previous work on a virally encoded fungal toxin, KP4, from Ustilago maydis and subsequently with the plant defensin, MsDef1, from Medicago sativa demonstrated that some of these proteins specifically blocked calcium channels in both fungi and animals. The results presented here demonstrate that KP4 and three plant defensins, MsDef1, MtDef2, and RsAFP2, all inhibit root growth in germinating Arabidopsis seeds at low micromolar concentrations. We have previously demonstrated that a fusion protein composed of Rab GTPase (RabA4b) and enhanced yellow fluorescent protein (EYFP) is dependent upon calcium gradients for localization to the tips of the growing root hairs in Arabidopsis thaliana. Using this tip-localized fusion protein, we demonstrate that all four proteins rapidly depolarize the growing root hair and block growth in a reversible manner. This inhibitory activity on root and root hair is not directly correlated with the antifungal activity of these proteins and suggests that plants apparently express targets for these antifungal proteins. The data presented here suggest that plant defensins may have roles in regulating plant growth and development. A. Allen and A.K. Snyder contributed equally.  相似文献   

17.
Plant enzyme activities in the rhizosphere potentially are a resource for improved plant nutrition, soil fertility, bioremediation, and disease resistance. Here we report that a border cell specific β-galactosidase is secreted into the acidic extracellular environment surrounding root tips of pea, as well as bean, alfalfa, barrel medic, sorghum, and maize. No enzyme activity was detected in radish and Arabidopsis, species that do not produce viable border cells. The secreted enzyme activity was inhibited by galactose and 2-phenylethyl 1-thio-β-d-galactopyranoside (PETG) at concentrations that altered root growth without causing cell death. A tomato galactanase encoding gene was used as a probe to isolate a full length pea cDNA clone (BRDgal1) from a root cap-border cell cDNA library. Southern blot analysis using full length BRDgal1 as a probe revealed 1–2 related sequences within the pea genome. BRDgal1 mRNA expression was analysed by whole mount in situ hybridization (WISH) and found to occur in the outermost peripheral layer of the cap and in suspensions of detached border cells. No expression was detected within the body of the root cap. Repeated efforts to develop viable hairy root clones expressing BRDgal1 antisense mRNA under the control of the CaMV35S promoter, whose expression in the root cap is limited to cells at the root cap periphery only during root emergence, were unsuccessful. These data suggest that altered expression of this enzyme is deleterious to early root development. The first two authors contributed equally to the completion of this project.  相似文献   

18.
棉花根系生长和空间分布特征   总被引:25,自引:0,他引:25       下载免费PDF全文
结合田间根钻取样和图像扫描分析方法, 研究了不同棉花品种根系的长度、直径和表面积动态及 0~ 10 0cm深和 0~ 4 0cm宽土壤范围内的空间分布特征。该方法与常规直尺测量结果相比相关系数R2 达到 0.899 (n =1318), 显示了较好的可靠性。研究结果表明, 棉花平均根长密度 (RLD) 在花铃期为 1.2 1~ 1.2 7mm·cm-3, 吐絮后降至 1.0 4~ 1.12mm·cm-3, 收花时为 0.76mm·cm-3 。棉花根平均直径在不同基因型间存在显著差异, 抗虫杂交棉的根直径最粗, 平均为 0.5 2mm ;早熟类型品种根直径较细, 平均为 0.36mm。在土壤深度上根直径的差异不显著, 但距棉行距离越远, 根的平均直径越小。在明确根系长度和直径动态规律的基础上, 提出了根表面积指数 (RAI) 的概念, 与地上部叶面积指数具有相似的含义和生物学意义, 且呈较好的指数相关关系 (R2 =0.779) 。RAI在生理发育时间 (PDT) 小于等于 4 0前, 其增长动态符合LOGISTIC生长规律 (R2 =0.84 9), 在PDT大于 4 0后, 呈线性递减趋势 (R2 =0.5 70~ 0.895 ), 且杂交抗虫棉的RAI在全生育期内均明显高于其它类型品种, 而早熟类型品种相对略低。RAI空间分布特征表现为, 开花前在浅根层内 (0~ 30cm) 分布最多, 花铃期以中层根系 (40~ 6 0cm) 为主, 吐絮后主要以深层 (70~ 10 0cm) 和距棉行较远的行间较多。研究结果为制定合理的施肥、灌溉措施提供了理论依据, 并量化了棉花根系的时空变化, 为进一步提高生长发育模拟模型的精度奠定了基础。  相似文献   

19.
Summary This study examined the effects of aggregate size on root impedance and developed an equation to describe the root pressure necessary to avoid deflection around an aggregate. This critical root pressure was predicted to increase with increasing aggregate size, decreasing root diameter, and decreasing deflection angle. In growth chamber experiments, maize (Zea mays L.) seedlings were grown in A horizon material of Groseclose silt loam (Clayey, mixed, mesic, Typic Hapludult). The soil had been moist sieved into different aggregate sizes (0–1, 1–2, 2–3, and 3–6 mm diameter). The larger aggregates did constitute a slight root impedance as roots were deflected around them. Diameters of roots grown in 3–6 mm aggregates increased significantly, whereas root lengths were not always signficantly decreased. The smaller aggregates did not impede root growth and were readily displaced by roots. Large aggregates were more of an impedance to lateral roots than to main axes.  相似文献   

20.
Summary A simple method for making detailed measurements of seedling root systems is described. Photocopies of root systems are traced over by an operator using a digitizing system attached to a microcomputer. The computer calculates and prints the lengths of axis, laterals and sublaterals for each root system. Accurate measurements can be achieved with a degree of speed and detail unobtainable by other methods.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号