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1.
伊洛河流域外来草本植物分布格局   总被引:2,自引:1,他引:2  
外来生物入侵及其防治已经成为生态学关注的重点和热点问题.目前的研究主要集中在外来入侵种上,然而入侵种仅占外来种中很少一部分,因此,研究外来种现有分布格局对研究生物入侵及其防治有重要意义.以伊洛河流域草本植物群落中的外来种为对象,沿河从河源地到入黄河口选取典型样地,在调查流域内草本植物群落中物种组成的基础上选取外来种,并对外来种种类组成及其分布格局进行研究.结果表明:流域内有外来草本植物27种,分属于15科,种类较多的科为菊科、苋科和豆科;引入方式以有意引种为主.流域横向不同生境间,河滩地在水流的养分富集、季节性洪水物理干扰及人为活动扰动作用下,呈现出受外来种分布较多,而受人类活动扰动最强且营养丰富的农田分布较小的分布格局;纵向环境梯度下,上游河源山地属于自然植被区,人为干扰较轻,且受外来种影响较小;中游丘陵区从自然生态系统向农业生态系统的过渡区域,人类活动的扰动有所加强;下游平原农业区,人类活动强烈,区域内以人工生态系统为主,群落物种组成简单但受外来种影响最大,受自然环境和人类活动的双重影响.不同物种在不同生境间差异明显,其中,小蓬草、钻叶紫菀和反枝苋广泛分布于3种生境中.总体上,伊洛河外来草本植物分布格局在自然因素的基础上强烈受人为因素的影响,呈现出从上游到下游逐渐增多的趋势.  相似文献   

2.
秦岭牛背梁植物物种多样性垂直分布格局   总被引:32,自引:0,他引:32  
基于秦岭山脉中段牛背梁自然保护区南北坡垂直样带51个样方的调查资料,利用植被数量分析方法(TWINSPAN和DCA)对牛背梁植物群落进行了分类和排序,并分析了植物物种多样性沿海拔梯度的分布格局。结果表明,牛背梁的植被群落具有明显的海拔梯度格局,从低海拔到高海拔依次分布有:锐齿槲栎(Quercus aliena var.acuteserrata)林,桦木(Betula spp.)林.巴山冷杉(Abis Jargesii)林和亚高山灌丛。海拔梯度是牛背梁山区制约植物群落分布的主要因子,而坡向和坡度则起到次要作用。对物种多样性的分析表明,物种总数、木本植物物种多样性和草本植物物种多样性在南北坡具有不同的海拔梯度格局。物种总数在南坡呈现单峰分布格局,而在北坡分布趋势不明显;木本植物物种多样性在南北坡具有相似的分布格局:在低海拔沿海拔梯度变化不明显,而在高海拔则随海拔上升而急剧下降;草本植物物种多样性在南北坡沿海拔梯度变化的规律不明显。β多样性沿海拔梯度先减少后增加,形成两端高中间低的格局,说明中海拔地区生境条件较为均一,低海拔地区的人为活动增加了生境的异质性,而高海拔地区的生态过渡特性增加了物种的更替速率以及群落的相异性。  相似文献   

3.
方康  徐国策  李鹏  王斌  陈新  马天文  魏全  马凌 《生态学报》2023,43(13):5571-5580
沉积物是河流生态系统中氮磷等物质循环的重要场所,而微生物是河流生态系统的重要组成部分,探究沉积物中微生物群落碳源利用特征和功能多样性对于河流生态环境保护具有重要意义。利用Biolog Eco微平板法、基于主成分分析、冗余分析阐明了大理河流域沉积物中微生物群落碳源利用强度和功能多样性变化特征及其影响因素。结果表明:(1)从流域上游到流域下游,沉积物中微生物碳源利用强度逐渐降低,与上游相比,支流、中游、下游沉积物中微生物碳源利用强度分别降低了13.4%、30.5%、30.7%。(2)沉积物中微生物群落功能多样性存在差异,沉积物中微生物群落功能多样性(Shannon-Wiener多样性指数)表现为上游 > 支流 > 中游 > 下游,常见物种优势度(Simpson多样性指数)则表现为下游 > 支流 > 中游 > 上游。(3)与微生物代谢活动相关性较高碳源为糖类,其次是氨基酸类,聚合物类、羧酸类、胺类、酚酸类与微生物代谢活动相关性较低。(4)沉积物中全氮、氨氮、硝氮、有机碳含量是影响微生物群落功能多样性和碳源利用特征差异的主要因素。流域沉积物中合适的碳、氮水平对维持河流水生态健康具有重要的意义。  相似文献   

4.
黄山陈村水库上游河源溪流的鱼类群落及其纵向梯度格局   总被引:1,自引:0,他引:1  
确定鱼类群落的分布格局及其对人类活动的响应,是合理保护、恢复和管理鱼类多样性的基础。基于2011年5月和10月自黄山陈村水库上游3条河源溪流共39个样点的调查数据,比较研究了溪流间鱼类群落及其纵向梯度格局的异同,着重探讨了人类活动对溪流鱼类群落纵向梯度格局的影响。研究结果显示,同人为干扰较轻的舒溪相比,人为干扰严重的浦溪和麻溪中水宽、底质和植被覆盖率等局域栖息地条件显著变化,这造成了后者的鱼类多样性显著下降及物种组成的显著变化,主要表现为敏感性的地方物种(如宽鳍鱲、光唇鱼、原缨口鳅等)数量减少、耐受性的广布物种(如泥鳅、麦穗鱼、高体鰟鲏等)数量增多。舒溪的鱼类物种数及其组成均与海拔显著相关,但这种"海拔-鱼类群落"关系在麻溪和浦溪中削弱甚至消失。底质、植被覆盖率对舒溪鱼类群落具有重要影响,但对浦溪和麻溪鱼类群落却无显著影响。研究结果表明,在子流域空间尺度上,诸如城镇化发展、土地利用、河道治理等人类活动可通过对局域栖息地条件的影响,导致溪流鱼类多样性下降及其物种组成的变化,破坏鱼类群落的纵向梯度格局,并改变栖息地与鱼类群落之间的联系。  相似文献   

5.
采用样线法调查了东辽河河岸带草本植物群落,分析了物种多样性特征,利用组平均聚类法和除趋势对应分析(DCA)分别对植物群落进行了分类和排序,探讨了影响东辽河河岸带草本植物群落分布的主要环境因子。结果表明:东辽河河岸带共有草本植物118种,属36科70属,草本植物的物种多样性自上游向下游呈现先增加后降低的变化趋势,而丰富度指数变化规律不显著,这与河流水文特征、河岸土壤基质类型、土壤含水量和人为干扰有关。聚类分析结果显示,东辽河河岸带草本群落可划分为11种类型,其中湿生植物群落占据优势。DCA排序轴与环境因子的相关性分析表明,海拔和河流等级是东辽河河岸带草本植物群落分布的重要影响因子。  相似文献   

6.
洞庭湖区鼠类群落的物种多样性分析   总被引:13,自引:0,他引:13  
张美文  王凯荣  王勇  李波 《生态学报》2003,23(11):2260-2270
通过对洞庭湖区黑线姬鼠褐家鼠主害区桃源的害鼠群落调查,揭示了平原农田生态类型区、丘陵农林复合生态类型区和山区林农复合生态类型区及其不同生境的鼠类群落的物种多样性。在人类干扰程度最高的平原生态类型区,鼠类群落的优势种突出,优势集中性指数最高,丘陵生态区次之,而具有大片森林、受干扰较低的山区林农复合生态区,优势集中性指数最低。物种多样性Shannon—Weiner指数和均匀性指数亦显示同样的规律:适度干扰的山区复合生态区的多样性指数最高,均匀性最好,丘陵生态区居中,平原生态区最低。不论何种生态类型区,农田生境鼠类群落的优势种都较突出,优势集中性指数也较高,群落多样性和均匀性较低;林地生境的优势集中性有较大下降,山区林地内的鼠种比丘陵区要多,优势集中性指数也较低,多样性指数和均匀度都有提高。林缘农田在同一生态类型不同生境内优势集中性最低、多样性指数和均匀性最高。比较不同生境鼠类群落的相似性,最不相似的群落是农田与受人类干扰较小的森林。这些现象说明人类的社会生产活动使害鼠群落的物种多样性降低、优势度下降、优势种突出、均匀性降低,形成了只利于少数几个种群栖息和生产发展的环境,最终导致少数种群的暴发,形成危害。但适度干扰能提高物种多样性。  相似文献   

7.
云南西部地区地带性植物群落物种多样性的地理分布格局   总被引:2,自引:0,他引:2  
利用样方数据和文献资料,探讨了云南西部地区地带性植物群落的物种多样性。结果表明:在纬度梯度上,从南到北,物种密度呈递减趋势;在海拔梯度上,从高海拔到低海拔,物种密度呈递增趋势;在经度梯度上,从东到西,物种密度呈递减格局。总体上,在群落尺度上,南部地区物种密度较高;北部地区,即滇西北地区物种密度相对较低,这可能与研究区域内热量和水分条件的空间分异有关,但热量因子可能扮演着更为重要的角色。海拔梯度上的物种变化速率远高于经度梯度和纬度梯度,这可能与海拔梯度上热量条件的变化速率远高于其他地理梯度有关。区域尺度上单位面积物种多样性的分布格局与群落尺度明显不同,这可能源于群落尺度上单位面积的物种多样性主要受制于能量水平;但在区域尺度上,单位面积的物种多样性可能与区域内的生境异质性有关。表明“尺度效应”在塑造物种多样性地理分布格局中的重要作用。  相似文献   

8.
伏牛山自然保护区物种多样性分布格局   总被引:9,自引:5,他引:4  
在伏牛山自然保护区典型地段设立样方,通过群落调查和多样性分析对物种多样性的垂直分布格局进行研究。发现:α多样性,乔木层在中海拔的落叶阔叶混交林带最高,灌木层随海拔升高稍呈上升趋势,草本层在低海拔次生林带和山顶矮林带物种多样性较高;β多样性总体上呈"~"型变化,在中海拔建群种发生更替的落叶阔叶混交林区最高,物种更替速率最快,其次是山顶附近。γ多样性大致沿海拔升高递减,以700m以下和过渡带落叶阔叶混交林区总物种丰富度最高。沿海拔梯度升高,水热组合发生变化,地带性植被总体上表现为由栓皮栎(Quercus variabilis)林向锐齿栎(Quercus aliena var.acuteserrata)林更替,在建群种发生更替的中海拔过渡带形成混交林带,短柄枹(Quercus glandulifera var.brevipetiolata)、槲栎(Quercus aliena)等夹杂其间在一些小生境中形成优势种群。总体上体现了过渡带具有高的物种多样性和更替速率,总物种丰富度隐含着沿海拔升高而降低的负相关关系。  相似文献   

9.
探索和揭示生物多样性的空间格局和维持机制是生态学和生物地理学研究的热点内容, 但综合物种、系统进化和功能属性等方面的多样性海拔格局研究很少。该文以关帝山森林群落为研究对象, 综合物种、谱系和功能α和β多样性指数, 旨在初步探讨关帝山森林群落多样性海拔格局及其维持机制。研究结果表明: 随着海拔的升高(1 409-2 150 m), 关帝山森林群落物种丰富度指数(S)、谱系多样性指数(PD)和功能丰富度指数(FRic)整体上表现出上升的趋势, 特别是海拔1 800 m以上区域。随着海拔的升高, 总β多样性(βtotal)和更替(βrepl)上升趋势明显, 而丰富度差异(βrich)则逐渐下降。不同生活型植物的物种、谱系和功能多样性海拔格局差异较大。随着海拔的升高, 草本植物S和物种多样性指数(H′)上升趋势高于木本植物。影响草本植物S分布的主要因素是地形因子, 而影响木本植物S分布的主要因素是历史过程。随着海拔的升高, 木本植物βtotal上升趋势要比草本植物明显。随着海拔的升高, 木本植物βreplβrich分别表现出单峰格局和“U”形格局, 而草本植物βreplβrich则分别表现出单调递增和单调递减的格局。随着环境差异和地理距离的增加, 群落间物种、谱系和功能β多样性显著增加。环境差异(环境过滤)对木本植物的β多样性具有相对较强的作用; 而环境差异(环境过滤)和地理距离(扩散限制)共同作用于草本植物的β多样性。  相似文献   

10.
溪流鱼类多样性沿着河流纵向梯度的空间分布规律已得到大量报道, 但这些研究大多聚焦基于物种组成的分类α多样性, 而有关分类β多样性和功能多样性的纵向梯度分布规律及其对人类干扰的响应研究较少。本文以青弋江上游3条人为干扰程度不同的河源溪流为研究区域, 比较研究了人为干扰对溪流鱼类功能α和β多样性及其纵向梯度分布格局的影响。结果显示, 人类干扰改变了河源溪流鱼类功能多样性的纵向梯度格局——由线性变化变为二项式分布。此外, 我们发现, 人为干扰导致土著种被本地入侵种取代, 且较强的土地利用和水污染排放可能增大环境的不连续性, 而群落周转和嵌套变化往往取决于环境的变化。尽管功能β多样性由嵌套成分主导, 但周转成分占比相对于人为干扰较小的溪流而言明显增加。人为干扰显著改变了受干扰溪流鱼类的物种组成和功能多样性, 且功能多样性的纵向梯度格局在不同的多样性指标上存在差异。本研究强调, 在评估人为干扰下多样性的变化时, 需要从多方面考虑, 包括空间尺度和多样性指标等。  相似文献   

11.
伊洛河河岸带生态系统草本植物功能群划分   总被引:10,自引:5,他引:5  
郭屹立  卢训令  丁圣彦 《生态学报》2012,32(14):4434-4442
植物功能群是对环境有相同响应和对主要生态系统过程有相似作用的组合。伊洛河是黄河中游南岸的一条重要水系,其河岸带生态系统不同生境类型中草本植物优势种变化明显,能较好地反映出植被与环境的动态关系。根据调查结果,结合出现次数和重要值,选取27种优势种进行种间联结及相关性分析。以$2检验为基础,结合联结系数AC和共同出现百分率PC来测定草本层优势种间的联结性,根据优势种间的联结性及其在不同生境中的变化异同,以优势种为主体划分伊洛河河岸带生态系统中草本植物功能群。结果表明,对27种草本植物优势种共划分了5组功能群:"广布型"、"湿生型"、"中旱生型"、"农田逃逸型"和"入侵型"。表明以优势种为主体对伊洛河河岸带生态系统草本植物进行功能群划分可行性高,有较强的代表性。同一功能群物种间表现出显著正联结性,一起出现在同一生境下的几率较大,在长期的生长演化过程中,能够适应相似的资源环境且对干扰有相似的响应。伊洛河河岸带生态系统由于长期的自然和人为干扰,加上外来物种的入侵,河岸带生态系统的生物多样性和生态安全面临着严峻的挑战。  相似文献   

12.
1. Few extensive lotic studies have examined patterns in the biodiversity of non‐biting midges (Diptera: Chironomidae) along major environmental gradients. Our aim was to fill this gap by describing patterns in species diversity, assemblage composition and distributions of midges across a boreal drainage basin. 2. We found that the diversity of midges, as measured by rarefied species richness, Fisher’s α and Pielou’s evenness, responded positively to stream size in regression analysis. By contrast, species density was most strongly correlated to a gradient in suspended solids and phosphorus in stream water, as well as macrophyte cover. Spatial variables were not significantly correlated with species diversity. 3. Midge assemblage composition was best explained by a model incorporating five composite environmental gradients in canonical correspondence analysis. The environmental gradients were stream size, macrophyte cover, alkalinity, nitrogen and suspended solids. Spatial variables did not overcome the effects of environmental gradients on assemblage composition. 4. Cluster analysis divided the 27 study sites into four groups with relatively similar midge assemblages. These groups were statistically significant in multi‐response permutation procedure, and 15 of the 49 midge taxa recorded varied significantly among the groups in indicator value analysis. Discriminant function analysis showed that stream size, macrophyte cover and habitat structure predicted 66.7% of sites into correct groups. 5. The information provided by the present analyses may be of considerable importance in conservation planning at the drainage basin level. The fact that species diversity and assemblage composition varied primarily along the stream size gradient suggests that sites belonging to the different size classes (first to fifth order) are needed to conserve the biodiversity of midges. The other environmental gradients should also be considered in conservation planning, because they explained significant amounts of variability in midge assemblage composition.  相似文献   

13.
采用样方调查法,研究了白龙江干旱河谷不同坡向主要灌丛群落沿着海拔梯度的结构特征、物种多样性的变化规律,旨在了解白龙江干旱河谷不同海拔梯度植被特征和物种多样性变化,为白龙江干旱河谷区域不同海拔植被恢复提供理论依据。研究结果表明:(1)不同海拔梯度同一坡向物种数不同,同一海拔不同坡向物种数也不同,随着海拔的升高不同坡向物种数表现为先增加后减少的趋势,同一海拔梯度内不同坡向主要植被类型也不同。(2)主要灌木群落α多样性在不同坡向随着海拔梯度的升高,表现出先升高后减小的趋势。不同坡向草本群落α多样性随着海拔的升高,也表现出先升高后减小的趋势。对主要灌丛α多样性指数进行相关性分析得物种丰富度指数对物种多样性贡献率最大,表现为丰富度指数(D1、D2)> 生态优势度指数(SN)> 种间机遇指数(H)> 群落均匀度指数(R)。(3)不同坡向主要灌丛群落β多样性Whittaker指数沿着不同海拔梯度变化不大,最大值出现在海拔1250~1650m;Routledge和Codyβ多样性指数在海拔1450~1650m出现最大值,但是大体呈现出波形变化。草本β多样性随着海拔的升高变化较大,阳坡植物的β多样性指数在海拔1050~1250m达到最大,阴坡和半阴半阳坡在海拔区间1250~1450m达到最大,半阴半阳坡的β多样性指数均大于阳坡。白龙江干旱河谷不同坡向、不同海拔梯度物种α多样性和β多样性都不同,且不同坡向随着海拔梯度的变化物种α多样性和β多样性呈一定的相关性,说明海拔和坡向是影响生物多样性主要因子之一。  相似文献   

14.
Wang Y J  Tao J P  Zhang W Y  Zang R G  Ding Y  Li Y  Wang W 《农业工程》2006,26(11):3525-3532
Human activities such as deforestation, cultivation, and overgrazing have contributed to the destruction of forest ecosystems in the upper Minjiang River basin for a long time, which has led to the reduction in forest coverage and biodiversity. On the Giant Panda Corridor of Tudiling in this basin, the effects of the existing disturbance regimes on plant communities after the vegetation restoration in the 1980s were assessed, and the community composition, the species diversity and their relationships with environmental factors significantly associated with the disturbance were analyzed using the transect sampling method, the two-way indicator species analysis (TWINSPAN) and the detrended canonical correspondence analysis (DCCA). The results were as follows: communities could be classified into six types, and species were clustered into four functional groups (responsive to disturbance, retarded disturbance, resistant to intermediate disturbance, and resistant to heavy disturbance) based on both TWINSPAN and DCCA. DCCA with species composition of plots is similar to that with species diversity of plots. The communities were separated into distinct groups along the DCCA axis, and this pattern was significantly correlated with environmental factors. Elevation differences, shape, slope, distance to roads, and the number of paths in the plots had an evident influence on the distribution of the species and communities. Environmental factors including slope, distance to roads, and the number of paths revealed the gradient of disturbance among the communities along the DCCA axis. High disturbance intensity caused significantly lower species diversity and inhibited the regeneration of vegetation compared with the more diverse undisturbed communities. Artificial restoration was more effective than natural restoration in maintaining high species diversity. The process of succession was inhibited in natural restoration because of the failure of tree establishment, growth, and survival during regeneration.  相似文献   

15.
1. Many studies have shown traditional species diversity indices to perform poorly in discriminating anthropogenic influences on biodiversity. By contrast, in marine systems, taxonomic distinctness indices that take into account the taxonomic relatedness of species have been shown to discriminate anthropogenic effects. However, few studies have examined the performance of taxonomic distinctness indices in freshwater systems. 2. We studied the performance of four species diversity indices and four taxonomic distinctness indices for detecting anthropogenic effects on stream macroinvertebrate assemblages. Further, we examined the effects of catchment type and area, as well as two variables (pH and total phosphorus) potentially describing anthropogenic perturbation on biodiversity. 3. We found no indications of degraded biodiversity at the putatively disturbed sites. However, species density, rarefied species richness, Shannon's diversity and taxonomic diversity showed higher index values in streams draining mineral as opposed to peatland catchments. 4. Of the major environmental gradients analysed, biodiversity indices showed the strongest relationships with catchment area, lending further support to the importance of stream size for macroinvertebrate biodiversity. Some of the indices also showed weak linear and quadratic relationships to pH and total phosphorus, and residuals from the biodiversity index‐catchment area regressions (i.e. area effect standardized) were more weakly related to pH and total phosphorus than the original index values. 5. There are a number of reasons why the biodiversity indices did not respond to anthropogenic perturbation. First, some natural environmental gradients may mask the effects of perturbation on biodiversity. Secondly, perturbations of riverine ecosystems in our study area may not be strong enough to cause drastic changes in biodiversity. Thirdly, multiple anthropogenic stressors may either increase or decrease biodiversity, and thus the coarse division of sites into reference and altered streams may be an oversimplification. 6. Although neither species diversity nor taxonomic distinctness indices revealed anthropogenic degradation of macroinvertebrate assemblages in this study, the traditional species diversity and taxonomic distinctness indices were very weakly correlated. Therefore, we urge that biodiversity assessment and conservation planning should utilize a number of different indices, as they may provide complementary information about biotic assemblages.  相似文献   

16.
长江流域兽类物种多样性的分布格局   总被引:1,自引:0,他引:1  
共记录了长江流域内兽类280种,隶属于11目36科135属,特有种和受威胁物种分别有14种和154种。根据兽类分布特点,依据山系和水系将长江流域分为19个区域,除了江源区外,物种丰富度、G-F多样性指数和特有种比例,从上游到下游区域总体趋势是随海拔降低逐渐降低,形成以四川盆地和沅江为分界线的3个数量级;利用Jaccard物种相似性系数对长江流域内19个区域进行聚类分析,发现整个流域分成4部分:江源区;横断山区、川西高原、云南高原、四川盆地和秦巴山区;贵州高原、江南丘陵、鄱阳湖平原和长江三角洲;淮阳山地、两湖平原和长江下游平原,基本反映了流域内自然地理环境及我国大陆地势三级台阶变化的特点。  相似文献   

17.
澜沧江-湄公河是东南亚最大的河流, 也是世界上淡水生物多样性最高的三大河流之一。由于特殊的地理位置和国际河流属性, 澜沧江-湄公河淡水鱼类的多样性现状仍缺乏系统的认识。本文在近20年调查的基础上, 系统整理了澜沧江-湄公河中上游32个支流或亚流域的淡水鱼类物种名录, 在此基础上对其种类组成和分布进行了分析, 并利用分类学多样性指数对澜沧江-湄公河中上游流域的物种多样性进行了评估。结果表明, 澜沧江-湄公河中上游共记录了淡水鱼类745种, 分属于2纲17目63科229属, 其中鲤形目鱼类451种, 占物种数的60.5%。分类学多样性指数显示, 从源头到中游, 淡水鱼类在分类阶元上的分布越来越均匀, 亲缘关系越来越远, 分类多样性越来越高。聚类分析(cluster analysis, CA)和多维尺度分析(multi-dimensional scaling, MDS)表明, 当Jaccard相似性系数为8.69时, 澜沧江-湄公河中上游32个亚流域可以分为源区、上游和中游3组; 相似性分析(ANOSIM)结果显示, 各组之间淡水鱼类组成差异显著(R = 0.877, P = 0.001)。相似性百分比分析(similarity percentage analysis, SIMPER)结果表明, 导致3组差异性的鱼类主要是鲤形目和鲇形目鱼类, 且随着地势阶梯的升高出现了科级、属级类群的替代。近几十年来, 随着流域各国人口的增长和经济的快速发展, 澜沧江-湄公河鱼类多样性和渔业资源面临严重威胁, 未来需加强流域内国家间合作, 在流域尺度上制定科学保护计划。  相似文献   

18.
Ecosystem resilience is the inherent ability to absorb various disturbances and reorganize while undergoing state changes to maintain critical functions. When ecosystem resilience is sufficiently degraded by disturbances, ecosystem is exposed at high risk of shifting from a desirable state to an undesirable state. Ecological thresholds represent the points where even small changes in environmental conditions associated with disturbances lead to switch between ecosystem states. There is a growing body of empirical evidence for such state transitions caused by anthropogenic disturbances in a variety of ecosystems. However, fewer studies addressed the interaction of anthropogenic and natural disturbances that often force an ecosystem to cross a threshold which an anthropogenic disturbance or a natural disturbance alone would not have achieved. This fact highlights how little is known about ecosystem dynamics under uncertainties around multiple and stochastic disturbances. Here, we present two perspectives for providing a predictive scientific basis to the management and conservation of ecosystems against multiple and stochastic disturbances. The first is management of predictable anthropogenic disturbances to maintain a sufficient level of biodiversity for ensuring ecosystem resilience (i.e., resilience-based management). Several biological diversity elements appear to confer ecosystem resilience, such as functional redundancy, response diversity, a dominant species, a foundation species, or a keystone species. The greatest research challenge is to identify key elements of biodiversity conferring ecosystem resilience for each context and to examine how we can manage and conserve them. The second is the identification of ecological thresholds along existing or experimental disturbance gradients. This will facilitate the development of indicators of proximity to thresholds as well as the understanding of threshold mechanisms. The implementation of forewarning indicators will be critical particularly when resilience-based management fails. The ability to detect an ecological threshold along disturbance gradients should therefore be essential to establish a backstop for preventing the threshold from being crossed. These perspectives can take us beyond simply invoking the precautionary principle of conserving biodiversity to a predictive science that informs practical solutions to cope with uncertainties and ecological surprises in a changing world.  相似文献   

19.
珠江水系鱼类群落多样性空间分布格局   总被引:14,自引:1,他引:13  
珠江是我国南方第一大河,是我国重要淡水渔业生产基地和水生生物资源基因库。珠江鱼类在维持生物多样性、提供鱼类种质资源方面举足轻重。但是到目前为止,关于其鱼类空间分布格局的研究甚少。特别是近几十年来各种水工建设和过度捕捞使得渔业资源急剧衰退,鱼类空间分布的研究显得尤为重要。2015年对珠江全流域13个站位进行了全面调查,共采集渔获物10119尾,隶属于94种72属17科。鲤科鱼类占显著优势,其次种类较多的依次为鲿科、鳅科。采用非度量多维标度排序(NMDS)方法对鱼类群落空间分布特征进行了分析,结果表明珠江鱼类被划分为3个类群,即以餐、南方拟餐、黄颡鱼等小型鱼类为主的中上游类群、以赤眼鳟、鲮鱼、广东鲂等中型鱼类为主的中下游类群和以罗非鱼为主的重要支流类群。同时发现中下游物种多样性高,上游及河口江段多样性低的格局。采用冗余分析方法(RDA)分析了鱼类多样性与环境因子的关系,发现年均气温、降雨量、年均径流量、河流宽度与透明度是珠江水系河流鱼类群落结构差异的主要影响因子,其中年均气温是影响鱼类群落分布的最关键因子之一。与历史资料对比后发现,珠江鱼类种类明显减少、空间分布也发生了巨大改变。研究是珠江水系野生渔业资源长期调查的一部分,研究结果将对渔业资源的多样性保护和可持续利用具有指导意义。  相似文献   

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