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1.
三江并流地区干旱河谷植物物种多样性海拔梯度格局比较   总被引:1,自引:0,他引:1  
在滇西北三江并流地区典型干旱河谷段, 在怒江、澜沧江和金沙江的东、西坡共设置了6条海拔梯度样带, 通过标准样地的植物群落调查, 分析各条样带植物的物种丰富度、物种更替率的海拔梯度格局, 并比较了地理和植被变量对分布格局的解释。干旱河谷植被带位于海拔3,000 m以下, 以灌丛和灌草丛为主, 其在各河谷的分布上限自西向东依次升高。植物物种丰富度的分布主要与海拔、流域、经纬度和植被带有关, 沿纬度和海拔梯度升高而显著增加的格局主要表现在草本层和灌木层, 灌木物种丰富度还呈现自西向东显著增加的趋势。怒江的灌木和草本种物种丰富度显著高于金沙江和澜沧江, 三条江的乔木种丰富度差异则不显著。森林带的样方草本物种丰富度显著低于灌草丛带样方, 并且还拥有后者没有的乔木种。不同样带的植物物种更替速率呈现了不一致的海拔梯度格局, 但均在样带海拔下部的灌草丛群落与海拔上部森林群落之间的交错带出现峰值。森林-灌草丛植被交错带在怒江样带处于海拔1,900-2,100 m处, 在澜沧江河谷位于海拔2,300-2,400 m, 在金沙江河谷位于海拔2,700-2,900 m。所有海拔样带的森林段或灌草丛段相对于同一样带不同植被段之间的物种更替程度为最小, 不仅小于同一流域不同样带相同植被段之间物种更替率的均值, 更小于所有样带相同植被段之间的更替率均值。在三条河流6条海拔样带的12个植被带段之间的物种更替变化中, 空间隔离因素可以解释34.2%, 而植被类型差异仅能解释不到0.5%。本研究结果显示了环境差异对不同植被类型物种丰富度的首要影响, 和各河流之间的空间隔离对植物群落构建和物种构成的主要作用。  相似文献   

2.
This study documents differences in fish assemblages for 32 freshwater streams located between 258 and 2242 m a.s.l. on the eastern slopes of the central range of the Colombian Andes. A total of 2049 fishes belonging to 62 species, 34 genera and 16 families were collected. Species richness declined rapidly with altitude; nearly 90% of the species were recorded between 250 and 1250 m a.s.l. Three of the four physico‐chemical variables, of the water, temperature, dissolved oxygen and pH, explained 53·5% of the variation in species richness along the altitudinal gradient, with temperature the most important (37·6%). An analysis of species composition showed that the distinctiveness of the fish fauna increased with elevation, with the greatest turnover observed between 1000 and 1750 m a.s.l. On this altitudinal gradient, turnover was dominated by the loss of species rather than gain, and dominance by just a few species was greater at higher elevations. Turnover was also observed along the altitudinal gradient in the structure of the three functional groups (torrential, pool and pelagic species). The study focused on understanding the pattern of diversity of fish communities inhabiting the Andes in Colombia. Anthropogenic effects on the altitudinal distribution of fish species in the region, however, are largely unknown and would require further investigations.  相似文献   

3.
Hu J  Xie F  Li C  Jiang J 《PloS one》2011,6(5):e19817
Quantifying spatial patterns of species richness is a core problem in biodiversity theory. Spiny frogs of the subfamily Painae (Anura: Dicroglossidae) are widespread, but endemic to Asia. Using spiny frog distribution and body size data, and a digital elevation model data set we explored altitudinal patterns of spiny frog richness and quantified the effect of area on the richness pattern over a large altitudinal gradient from 0-5000 m a.s.l. We also tested two hypotheses: (i) the Rapoport's altitudinal effect is valid for the Painae, and (ii) Bergmann's clines are present in spiny frogs. The species richness of Painae across four different altitudinal band widths (100 m, 200 m, 300 m and 400 m) all showed hump-shaped patterns along altitudinal gradient. The altitudinal changes in species richness of the Paini and Quasipaini tribes further confirmed this finding, while the peak of Quasipaini species richness occurred at lower elevations than the maxima of Paini. The area did not explain a significant amount of variation in total, nor Paini species richness, but it did explain variation in Quasipaini. Five distinct groups across altitudinal gradient were found. Species altitudinal ranges did not expand with an increase in the midpoints of altitudinal ranges. A significant negative correlation between body size and elevation was exhibited. Our findings demonstrate that Rapoport's altitudinal rule is not a compulsory attribute of spiny frogs and also suggest that Bergmann's rule is not generally applicable to amphibians. The study highlights a need to explore the underlying mechanisms of species richness patterns, particularly for amphibians in macroecology.  相似文献   

4.
Species richness patterns along altitudinal gradients are well-documented ecological phenomena, yet very little data are available on how environmental filtering processes influence the composition and traits of butterfly assemblages at high altitudes. We have studied the diversity patterns of butterfly species at 34 sites along an altitudinal gradient ranging from 600 to 2,000 m a.s.l. in the National Park Berchtesgaden (Germany) and analysed traits of butterfly assemblages associated with dispersal capacity, reproductive strategies and developmental time from lowlands to highlands, including phylogenetic analyses. We found a linear decline in butterfly species richness along the altitudinal gradient, but the phylogenetic relatedness of the butterfly assemblages did not increase with altitude. Compared to butterfly assemblages at lower altitudes, those at higher altitudes were composed of species with larger wings (on average 9 %) which laid an average of 68 % more eggs. In contrast, egg maturation time in butterfly assemblages decreased by about 22 % along the altitudinal gradient. Further, butterfly assemblages at higher altitudes were increasingly dominated by less widespread species. Based on our abundance data, but not on data in the literature, population density increased with altitude, suggesting a reversed density–distribution relationship, with higher population densities of habitat specialists in harsh environments. In conclusion, our data provide evidence for significant shifts in the composition of butterfly assemblages and for the dominance of different traits along the altitudinal gradient. In our study, these changes were mainly driven by environmental factors, whereas phylogenetic filtering played a minor role along the studied altitudinal range.  相似文献   

5.
Biodiversity patterns of vascular plant species were studied along altitudinal gradients in the Faroe Islands. Plants were sampled from five different mountains (150–856 m a.s.l.) at 50 m altitudinal intervals. Included in the study were 107 vascular plant species. In order to compare only altitudes with the same number of plots, three different analyses were carried out. One analysis included five mountains from 250 to 750 m a.s.l., one had three mountains from 150 to 750 m a.s.l., and the last one had two mountains from 750 to 850 m a.s.l. The patterns of biodiversity were evaluated on the basis of species richness as the total number of species at each altitudinal interval, as species turnover between altitudes and in relation to the Shannon‐Wiener index. Similar patterns were found for species richness in the three analyses, although richness was higher along the whole transect when five mountains were included. For the Shannon‐Wiener index, only small differences were found among the three analyses. A maximum was seen at 250 m a.s.l. and again at 500 m a.s.l. both in richness and in the Shannon‐Wiener index. Maximum species turnover was found at mid‐altitudes. Total vegetation cover followed the same pattern as richness. In addition to climate, the altitudinal variation of biodiversity may be affected by grazing.  相似文献   

6.
1. Describing and understanding patterns in biological diversity along major geographical gradients is an important topic in ecology. Samples collected from a large number of physically and chemically comparable stream sites along a 4000 m gradient of altitude in the Andes of Ecuador served to characterise patterns of family richness of aquatic macroinvertebrates at the scale of the stream site (local) and at that of discrete altitudinal zones. 2. Both mean local and zonal family richness decreased by about 50% from sea level to 4000 m a.s.l. Local richness declined linearly, while zonal richness remained constant from sea level up to a threshold altitude of about 1800 m, whereafter it decreased. 3. From sea level to 1800 m few families were lost from zonal richness and few were gained. From 1800 to 3800 m the decrease in the number of families was accounted for by a loss of families present in lowland streams, with few new families gained. Hence, there was relatively little turnover of families along the entire gradient. 4. The diverging pattern of local and zonal richness was caused by sporadically occurring families inflating zonal richness at mid‐altitudes. If the sporadic families were represented by the same species found commonly in the lowlands, then the mid‐altitudinal zonal richness would be maintained by a ‘rescue effect’. More probably, however, the sporadically occurring families found at mid‐altitudes are each represented by new species replacing each other along the gradient, the families progressively diminishing in species richness and occurrence as the overall temperature tolerance of the family is approached. 5. This study demonstrates that spatial scale affects altitudinal patterns in the taxonomic richness of stream invertebrates. It also showed that family‐level identification can facilitate interpretation of sources and sinks of biodiversity along geographic gradients.  相似文献   

7.
Differences in vascular plant species richness; along the altitudinal gradient in the Aurland area of western Norway have been investigated. Based on field surveys, as complete lists as possible of all vascular plants have been compiled for each 100 m altitudinal band, from sea level to the highest mountain (1764 m). For each of the 18 altitudinal bands, climatic data have been estimated. A total of 444 vascular plant species were recorded. Highest species richness (263 species) occurred in the 600–700 in band, whereas the uppermost band had only 10 species. There are minor differences in species number between the altitudinal bands < 1000 m. Partial least squares regression shows that species richness for the overall altitudinal gradient is well predicted by mean July and January temperatures and mean annual precipitation. Species turnover is highest in the 100–200 m. 600–700 m. and 1400–1500 m altitudinal bands. In terms of the gradient in summer temperature, the study supports the generally assumed linear relationship between July temperature and the number of vascular plant species between 700 and 1500 m corresponding with a mean July temperature range of 7–11°C. The study shows a decrease of ca 30 vascular plant species with a 1°C decrease in mean July temperature, and that the “climatic vascular plant limit” is here estimated to occur at a mean July temperature of 2.4°C. Above 1500 and below 700 m. species number is lower than expected based on summer iemperature conditions alone. The 700–800 m band represents the highest floristic difference compared to the other bands. Ordination and classification analyses of the floristic compositional data of all the bands highlight the 600–800 and 1500–1600 m altitudinal bands as the major biotic boundaries along the gradient. No major discontinuity in species richness, composition, or turnover was consistently found, however, at the 1100–1200 m band representing the forest-limit ecotone in Aurland.  相似文献   

8.
Biodiversity pattern and life-form spectra were studied along a 3,000 m altitudinal gradient from a semi-desert area to the alpine peak of Tochal Mountain. The gradient is located on the southern slopes of Central Alborz with a Mediterranean continental climate. DCA ordination was applied to 1,069 relevés and 7 quantitative variables to discover the relation of diversity and altitude. A biodiversity pattern was obtained by relating values for species richness and Shannon-Wiener’s index to 100-m altitudinal sections. Altitude was determined as the major ecological gradient. Both diversity indices are negatively correlated with altitude and show a decreasing trend beyond a peak in species richness at 1,800–1,900 m a.s.l. towards a very low diversity in the high alpine zone. The biodiversity peak does not match with the potential tree line in the area (2,500–3,000 m a.s.l.). The high diversity in foothills can be related to habitat heterogeneity, longer suitable climatic conditions, and diverse disturbance factors, while unfavorable conditions at high-altitude alpine and low-altitude desert areas reduce the number of species at both extremes. Life-form patterns clearly change along altitudinal gradient. Annuals with decreasing trend, and hemicryptophytes and chamaephytes with increasing trend along the altitudinal gradient are notable patterns of life form in the area. Temperature, soil moisture and nutrients are the main factors that explain the ecological influence of altitude on species diversity and life-form patterns in the semi-arid steppe vegetation of the area.  相似文献   

9.
Roadside plant communities were studied along two roads following an altitudinal gradient in Gran Canaria and Tenerife (Canary Islands). Our aim was to investigate variation in plant species richness, particularly of the alien flora, along a gradient from coastal shrubland to summit vegetation (1950 m a.s.l. in Gran Canaria, 2300 m in Tenerife) in relation to variation in habitat factors (altitude, habitat structure, roadside disturbance, distance to urban nuclei). We compared different species groups that were classified in terms of their biogeographical status, origin and life form. Altitude was the most important factor determining species richness and composition along both roadside transects. Alien plants showed a unimodal distribution pattern along the altitudinal gradient, with less species and lower abundance at low and high altitudes, and highest abundance at intermediate altitude. Alien plant species were also relatively more frequent near urban centres. The number of native and alien species was significantly positively correlated along the altitudinal gradient. Both alien and native, non-endemic species showed differences in their distribution along the altitudinal gradient according to their biogeographical affinities and climatic tolerances. Despite considerable differences in species pools these patterns were consistent among the two islands. Environmental (abiotic) stress is proposed as a primary, altitude-related factor acting as a filter against most alien plants at coastal and high-mountain altitudes. A higher frequency or intensity of disturbance at intermediate altitudes may be a further causal factor promoting alien plants in this zone. Future management efforts to control alien plants along roads should, therefore, concentrate on intermediate altitudinal zones of the higher Canary Islands.  相似文献   

10.
Aims The fauna of mountains and their surrounding regions are likely to be influenced principally by two biological processes: horizontal colonization along similar altitudinal levels by elements originating from lineages inhabiting higher latitudes; and vertical colonization by lineages from the same latitude, but at lower altitudes. We examine whether the expected patterns derived from the latter process can be observed in mountain dung beetle assemblages. Specifically, we study the variation in species composition and richness with altitude in five regions spanning elevation gradients, analysing whether the altitudinal rates of change in the number of species and genera differ, and whether beta‐diversity scores for adjacent sites in each altitudinal gradient are different for species and genera. Location Eastern Cordillera of the Colombian Andes. Methods Field work was carried out in 1997–99 at 27 sites in five regions with elevation gradients, with 10–32 pitfall traps placed in each site. For each altitudinal level the numbers of species and genera were analysed with respect to altitude, and the slope of the linear regression between these variables was calculated. The slope of the curve of the altitude against the cumulative number of species and genera was also calculated for each altitudinal gradient to describe the compositional change between adjacent sites (beta diversity). Species and generic slopes were compared using analysis of covariance. The turnover of species along each altitudinal gradient was measured using presence/absence data and Cody's beta‐diversity index between adjacent pairs of sites. A cluster analysis was used to detect faunistically homogeneous groups of localities. Results Species richness always decreased with altitude, although the slopes did not differ significantly from zero. The number of genera also decreased with increasing altitude, but generally at a significantly slower rate than for species. Variation in the species beta‐diversity scores between altitudinal levels did not follow a homogeneous pattern in the different regions. Two main altitudinal groups of sites with a boundary c. 1500–1750 m a.s.l. can be detected with respect to faunistic similarity. Low‐ and mid‐altitude sites are inhabited by all of the genera (19) and 80% of all species collected. Eight genera and 61 species (c. 60% of the total) are unable to inhabit high‐altitude sites, and only 20 species appear to be exclusive to these high‐altitude environments (> 2000 m a.s.l.). Main conclusions The dominant processes explaining dung beetle composition in the high north‐eastern Andean mountains are probably those of vertical colonization. The limited role of horizontal colonization processes, or colonization from northern or southern lineages, could be a consequence of the isolation and recent geological origin of these mountains.  相似文献   

11.
We studied the altitudinal patterns of plant species richness and examined the effects of geometric constraints, area, and climatic factors on the observed richness patterns along the ridge of the Baekdudaegan Mountains, South Korea. Rapoport’s altitudinal rule was evaluated by examining the relationship between altitudinal range size and midpoint. We also examined the latitudinal effect on species richness. Plant data were collected from 1,100 plots along a 200–1,900 m altitudinal gradient along the ridge of the Baekdudaegan. A total of 802 plant species from 97 families and 342 genera were found. The altitudinal patterns of plant species richness along the ridge of the Baekdudaegan depicted distinctly hump-shaped patterns, although the absolute altitudes of the richness peaks vary somewhat among plant groups. While the mid-domain effect (MDE) was the most powerful explanatory variable in simple regression models, species richness was also associated with climatic factors, especially mean annual precipitation (MAP) and temperature (MAT) in multiple regression models. The relative importance of the MDE and climatic factors were different among plant groups. The MDE was more important for woody plants and for large-ranged species, whereas climatic factors were better predictors for total and herbaceous plants and for small-ranged species. Rapoport’s altitudinal rule and a latitudinal effect on species richness were not supported. Our study suggests that a combined interaction of the MDE and climatic factors influences species richness patterns along the altitudinal gradient of the Baekdudaegan Mountains, South Korea.  相似文献   

12.
Aim Biodiversity patterns along altitudinal gradients are less studied in aquatic than terrestrial systems, even though aquatic sites provide a more homogeneous environment independent of moisture constraints. We studied the altitudinal species richness pattern for planktonic rotifers in freshwater lakes and identified the environmental predictors for which altitude is a proxy. Location Two hundred and eighteen lakes of Trentino–South Tyrol (Italy) in the eastern Alps; lakes covered 98% (range 65–2960 m above sea level) of the altitudinal gradient in the Alps. Methods We performed: (1) linear regression between species richness and altitude to evaluate the general pattern, (2) multiple linear regression between species richness and environmental predictors excluding altitude to identify the most important predictors, and (3) linear regression between the residuals of the best model of step (2) and altitude to investigate any additional explanatory power of altitude. Selection of environmental predictors was based on limnological importance and non‐parametric Spearman correlations. We applied ordinary least squares regression, generalized linear, and generalized least squares modelling to select the most statistically appropriate model. Results Rotifer species richness showed a monotonic decrease with altitude independent of scale effects. Species richness could be explained (R2= 51%) by lake area as a proxy for habitat diversity, reactive silica and total phosphorus as proxies for productivity, water temperature as a proxy for energy, nitrate as a proxy for human influence and north–south and east–west directions as covariates. These predictors completely accounted for the species richness–altitude pattern, and altitude had no additional effect on species richness. Main conclusions The linear decrease of species richness along the altitudinal gradient was related to the interplay of habitat diversity, productivity, heat content and human influence. These factors are the same in terrestrial and aquatic habitats, but the greater environmental stability of aquatic systems seems to favour a linear pattern.  相似文献   

13.
Elevational patterns of species richness and their underlying mechanisms have long been a controversial issue in biodiversity and biogeographical research, and several hypotheses have been proposed in the past decades. Local and regional studies have suggested that area and geometric constraint are two of major factors affecting the elevational pattern of species richness. In this study, using data of seed plants and their distribution ranges and a Digital Elevation Model data set, we explored altitudinal patterns of seed plant richness and quantified the effects of area and the mid-domain effect (MDE) on the richness patterns in a high mountain area, Gaoligong Mountains (ranging from 215 m to 5791 m a.s.l.) located in south-eastern Tibet, China. The results showed that richness and density (richness/log-transformed area) of seed plants at species, genus, and family levels all showed hump-shaped patterns along the altitudinal gradient. The altitudinal changes in richness of species with three different range sizes (< 500 m, 500–1500 m, and > 1500 m), species of different plant life-forms (trees, shrubs, and herbs), and endemic species further confirmed this finding. Analysis of Generalized Linear Model depicted that although the area of each elevational band was always in high correlation with the species richness, the MDE could explain 84.9%, 33.8%, 83.8%, and 84.5% of the total variation in richness for all species and the three species groups with different range sizes, respectively. This suggests that the MDE significantly influences the patterns of species richness and is likely be stronger for broad-ranged species than for narrow-ranged ones in the Gaoligong Mountains.  相似文献   

14.
《Acta Oecologica》2006,29(3):241-246
Species richness patterns of ground-dwelling vascular plants, bryophytes, and lichens were compared along an altitudinal gradient (310–1135 m a.s.l.), in western Norway. Total species richness peaked at intermediate altitudes, vascular plant species richness peaked immediately above the forest limit (at 600–700 m a.s.l.), bryophyte species richness had no statistically significant trend, whereas lichen richness increased from the lowest point and up to the forest limit, with no trend above. It is proposed that the pattern in vascular plant species richness is enhanced by an ecotone effect. Bryophyte species richness responds to local scale factors whereas the lichen species richness may be responding to the shading from the forest trees.  相似文献   

15.
Unraveling how climate change impacts the diversity and distribution patterns of organisms is a major concern in ecology, especially with climate-sensitive species, such as dung beetles. Often found in warmer weather conditions, beetles are used as bio-indicators of environmental conditions. By using an altitudinal gradient as a proxy for climate change (i.e., space-for-time substitution), we assessed how changes in climatic variables, such as temperature and precipitation, impact patterns of dung beetle diversity and distribution in the Peruvian Andes. We recorded dung beetle diversity using three different types of baits, feces, carrion, and fruits, distributed in 18 pitfall traps in five different altitudinal sites (from 900 to 2500 m, 400 m apart from each other) in the rainy and dry season. We found that (i) dung beetle richness and abundance were influenced by the climate gradient, (ii) seasonality influenced beetle richness, which was high in the wet season, but did not influence abundance, (iii) dung beetle richness and abundance fit to a hump-shaped distribution pattern along the altitudinal gradient, and (iv) species richness is the beta-diversity component that best describes the composition of dung beetle species along the altitudinal gradient. Our data show that the distribution and diversity of dung beetles are different at larger scales, with different patterns resulting from the response of species to both abiotic and biotic factors.  相似文献   

16.
高黎贡山种子植物物种丰富度沿海拔梯度的变化   总被引:27,自引:4,他引:23  
物种丰富度沿海拔梯度的分布格局成为生物多样性研究的热点。为探讨中尺度区域物种丰富度沿海拔梯度的分布,本文以高黎贡山为研究对象,利用该地区的地方植物志资料,结合通过GIS生成的区域数字高程模型(DEM)数据,分析了该区域全部种子植物和乔木、灌木、草本三种生活型种子植物物种丰富度的垂直分布格局以及物种密度沿海拔梯度的变化特征。结果表明:(1)全部种子植物和不同生活型植物物种丰富度随着海拔的升高呈现先增加后减小的趋势,最大值出现在海拔1500—2000m的范围;(2)物种密度与海拔也呈现单峰曲线关系;(3)物种丰富度和物种密度分布格局的形成主要受海拔所反映的水、热状况组合以及物种分布的边界影响。  相似文献   

17.
《Journal of Asia》2014,17(2):161-167
Two diversity patterns (hump-shaped and monotonic decrease) frequently occur along altitude or latitude gradients. We examined whether patterns of ant species richness along altitudes in South Korea can be described by these patterns and whether ranges of ant species follow Rapoport's altitudinal rule. Ants on 12 high mountains (> 1100 m) throughout South Korea (from 33° N to 38° N) were surveyed using pitfall traps at intervals of 200–300 m altitude. The temperatures at the sampling sites were determined from digital climate maps. Ant species richness decreased monotonically along the altitudinal gradient and increased along the temperature gradient. However, species richness of cold-adapted species (highland species) showed a hump-shaped pattern along altitude and temperature gradients. The altitude and temperature ranges of ant species followed Rapoport's rule. Sampling site temperature ranges were significantly correlated with coldness. Therefore, Rapoport's rule can be explained by high cold-tolerance of species inhabiting high altitudes or latitudes.  相似文献   

18.
Wang  Guohong  Zhou  Guangsheng  Yang  Limin  Li  Zhenqing 《Plant Ecology》2003,165(2):169-181
We studied the distribution pattern, species diversity and life-formspectra of plant communities along an altitudinal gradient in the mid-sectionofthe northern slopes of Qilianshan Mountains by means of multivariate analyses.Two data sets (167 species × 75 plots, 10 environmental variables ×75 plots), originated from the fieldworks in 1998–1999, were subjected toTWINSPAN and DCCA, resulting in 8 major plant communities: 1)Asterothamnus centraliasiaticus–Halogetonarachnoideus desert grassland on azonal substrates from 1450 to 1600m and 2) zonal Reaumuria soogorica desertgrassland on gravels from 1470 to 1900 m; 3) Stipaprzewalskii–Stipa purpurea montane grassland from 2200 to 2900m; 4) Polygonum viviparum alpine grasslandfrom 2900 to 3700 m; 5) Caraganastenophylla–Ajaniafruticulosa dry-warm shrubland from 2350 to 2800 m; 6)Sabina przewalskii mid-wet warm forest from 2700 to 3300m; 7) Picea crassifolia cold coniferousforestfrom 2450 to 3200 m; 8) Caragana jubatawet-cold alpine shrubland from 3100 to 3700 m. Species diversityand species richness of both grasslands and forests peaked at the intermediateportion of the elevational gradient. Evenness might be strongly influenced byeither biotic or abiotic factors at a local scale, while seems quiteindependentof an elevational gradient at landscape scales. Beta-diversity decreased from1500 to 3700 m, indicating that species turnover declined withincreased elevation. Both richness of life-form and total species richness in agiven altitudinal belt (gamma-diversity) peaked at intermediate elevations,while relative species richness of different life-form varied differently alongthe altitudinal gradient.  相似文献   

19.
Aim To study the altitudinal variation of ground spiders (Araneae, Gnaphosidae) of Crete, Greece, as far as species composition, species richness, activity and range of distribution are concerned. Location Altitudinal zones (0–2400 m) along the three main mountain massifs of the island of Crete. Methods Thirty‐three sampling sites were located from 0 to 2400 m a.s.l. on Crete, and sampled using pitfall traps. Material from the high‐activity period of Gnaphosidae (mid‐spring to mid‐autumn) was analysed. Sampling sites were divided into five altitudinal zones of 500 m each. Statistical analysis involved univariate statistics (anova ) and multivariate statistics, such as multidimensional scaling (MDS) and cluster analysis (UPGMA) using binomial data of species presence or absence. Results Species richness declines with altitude and follows a hump‐shaped pattern. The activity pattern of the family, as a whole, is not correlated with altitude and is highly species‐specific. In the highest zone, both species richness and activity decline dramatically. The altitudinal range of species distribution increases with altitude. On the Cretan summits live highly tolerant lowland species and isolated residents of the high mountains of Crete. Two different patterns of community structure are recorded. Main conclusions Communities of Gnaphosidae on Crete present two distinct structures following the altitudinal gradient, these being separated by a transitional zone between 1600 and 2000 m. This study supports previous results which show a hump‐shaped decline in species richness of Gnaphosidae along altitudinal gradients, leading to a peak at 400–700 m, where an optimum of environmental factors exists. This makes this zone the meeting point of the often opportunistic lowland species with the older and most permanent residents of the island. Rapoport's rule on the positive correlation of the altitudinal range of species distributions with altitude is also supported. The high activity recorded for the species that persist on the high mountains of Crete is indicative of a tolerant arachnofauna, and is considered to result from relaxation of competitive interactions with other species. This is related to a reduction in species numbers, shortening of the activity period on high mountains and the unique presence of high mountain species that thrive only there. As shown in our study, strategies to cope with altitude are species‐specific. Therefore, there cannot exist one single model to describe how animals react to the change in altitude, even under the same environmental conditions.  相似文献   

20.
Petr Sklenář 《Plant Ecology》2006,184(2):337-350
Altitudinal variation of the zonal superpáramo vegetation was studied between 4300 and 4630 m to test a possible occurrence of a fine altitudinal zonation within the superpáramo belt. A rectangular grid of 1 m2 sample plots was established; 25 replicate plots separated by a 3 m space were located along a 100 m long transect parallel to the contours, and there were 17 such transects separated by 20 m of altitude. Species were scored using a 7-grade cover scale and basic environmental data were gathered for each sample. Major changes occur over a short altitudinal range, at around 4400 m, which corresponds to a transition between the lower and upper superpáramo. Species richness sharply declines but species turnover (per altitude) increases along the altitudinal gradient. The correlation between richness and bare ground or rock cover is negative, but the correlation to rocks becomes positive above 4500 m. Species from lower altitudes tend to have narrower altitudinal range, although a large number of species appear to be indifferent to altitude. Direct ordination analyses indicate that high-altitude species show stronger correlation to environmental variables, especially rock, than species from lower altitudes. TWINSPAN cluster analysis delimited 15 groups of samples. There is a change in the clustering pattern along the altitudinal gradient from a horizontal (i.e., within altitude) to vertical (i.e., across altitude) arrangement of the cluster groups, although this pattern is partly obscured at the highest altitudes due to a large number of empty samples. MANOVA tests for samples from adjacent altitudinal levels indicate two distinct altitudinal breaks at lower altitudes, corresponding to the Loricaria-belt in lower superpáramo and the transition between lower and upper superpáramo, while no indication of a zonation was found in upper superpáramo.  相似文献   

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