澜沧江中游水生昆虫生活史和生态学性状多样性的海拔格局: 气候和土地利用的影响

物种通过功能性状响应环境变化, 探究群落功能性状多样性的海拔格局是揭示生物多样性空间分布格局和形成机制的重要研究内容。气候变化和土地利用是影响溪流生物多样性变化及其群落构建的重要因素, 然而气候和土地利用沿海拔梯度如何影响水生昆虫功能性状垂直分布格局的系统研究仍旧比较缺乏。本文基于2016年和2018年在云南澜沧江中游1,000-3,000 m海拔共56个溪流样点的水生昆虫群落调查数据, 利用线性和二次回归模型探索并比较了生活史性状(化性、生活史快慢、成虫寿命)和生态学性状(营养习性、生活习性、温度偏好)的群落加权平均性状多样性指数沿海拔梯度的分布特征, 并通过随机森林模型解析流域尺度气候和土地利用变量对生活史和生态学性状多样性垂直分布格局的影响。结果表明: 生活史性状中, 少于1世代、无季节性、慢季节性、成虫寿命长等性状多样性沿海拔梯度呈显著的“U”型分布格局, 而快季节性和成虫寿命极短多样性呈显著的单峰型海拔格局, 成虫寿命短多样性呈显著递增的海拔格局。生态学性状中, 温度偏好多样性与海拔梯度无关, 附着者和爬行者的多样性沿海拔梯度分别呈显著的递增和“U”型格局, 滤食者、植食者和捕食者的多样性分别呈显著递增、递减和“U”型海拔格局。随机森林模型分析结果表明, 气候和土地利用对生活史性状多样性的解释量高于对生态学性状多样性的解释量, 年平均温度和农业面积百分比是共同的关键因素。综上, 水生昆虫群落功能性状多样性海拔格局存在差异, 主要受不同自然环境梯度和人类干扰因素驱动。研究结果可为制定澜沧江流域生物多样性保护对策提供理论基础。     

钱塘江中游水生昆虫群落功能多样性对土地利用变化的响应

基于11个反映水生昆虫生活史、对外界抵抗力和生理特征的生物学性状,应用目前国际上通用的fourth-corner统计方法,系统研究了浙江省钱塘江中游流域水生昆虫功能多样性对土地利用变化的响应.结果表明： 部分生物学性状对土地利用变化敏感,且其随人类干扰强度的变化所发生的改变与预期吻合,其最大个体长度逐渐下降,呼吸方式从以鳃呼吸为主转变为以表皮呼吸为主,掘穴者数量显著增加.参照点的功能多样性指数(Rao值)显著高于干扰点(P<0.001).说明人类活动引起的土地利用变化导致溪流水质和栖境质量下降,引起群落的变异和对生物性状组成的筛选,最终导致水生昆虫群落功能多样性改变.生物性状及功能多样性是未来评价生态健康的潜在指标.     

北京东灵山土壤动物多样性海拔格局的尺度推绎规律

识别群落内部各类群多样性格局的复杂性是生态学家面临的挑战,而尺度推绎规律是揭示复杂生态结构的有效途径之一.本研究利用多重分形的方法探索了不同海拔土壤动物多样性格局的尺度推绎规律,对比分析了凋落物层和土壤层之间多重分形谱的差异.结果 表明:与之前对植物群落的分析结果相似,土壤动物多样性尺度推绎规律同样具有幂律特征,如丰富...     

山西关帝山森林群落物种、谱系和功能多样性海拔格局

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(β_total)和更替(β_repl)上升趋势明显, 而丰富度差异(β_rich)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β_total上升趋势要比草本植物明显。随着海拔的升高, 木本植物β_repl和β_rich分别表现出单峰格局和“U”形格局, 而草本植物β_repl和β_rich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。     

香溪河水生昆虫功能性状及功能多样性空间格局

近年来,生物多样性研究已从群落物种多样性拓展至功能多样性层面,使用功能性状表征功能组成及功能多样性是当前底栖动物生态学研究的热点之一。物种功能性状对环境变化敏感,对群落和种群沿环境梯度的演替具有许多潜在的指示作用。为了解香溪河水系水生昆虫功能性状空间分布格局及环境因子对功能多样性的影响,于2005年12月及2006年1月、2月对该水系的香溪河、九冲河、高岚河、古夫河4条河流的水生昆虫进行了调查,并对理化指标进行了测定;参考相关文献资料,本研究选择化性、漂移性、游泳能力、吸附能力、形状、个体大小、流态偏好、温度偏好、生活型、营养习性等10个功能性状纳入分析。研究结果发现,香溪河水系共鉴定水生昆虫127种,四节蜉(Baetis sp.)、高翔蜉(Epeorus sp.)、短尾石蝇(Nemoura sp.)为区域优势分类单元,相对丰度分别为38.6%、9.1%、6.7%;4条河流间优势物种组成差异较大。10个功能性状中相对丰度最高的等级性状分别为1世代/a(Volt2)、高漂移率(Drft3)、无游泳能力(Swim1)、无吸附能力(Atch1)、流线型(Shpe1)、小型个体(Size1)、沉积/侵蚀流态兼好型(Rheo2)、广温型(Ther2)、附着型(Habi4)、收集者(Trop1);单因素方差分析及独立样本T检验表明,化性、附着能力、大小、流速偏好、温度偏好、漂移性、生活型、营养习性等性状级别间差异显著,而游泳能力、形状性状等级间无显著差异。对10个功能性状的33个等级性状在4条河流间相对丰度的差异性进行研究,结果发现,Volt1、Drft2、Swim2、Atch1、Atch2、Size3、Rheo1、Ther3、Habi2、Habi3、Trop3、Trop5等12个等级性状相对丰度在4条河流间差异显著。功能性状多样性、树状图功能多样性用来描述4条河流功能多样性,结果表明,功能性状多样性指数均值在古夫河、高岚河、九冲河、香溪河分别为2.8、3.2、6.9和5.4;树状图功能多样性指数均值在分别为4.8、5.7、11.1、8.8。功能冗余度均值在4条河流分别为2.9、3.4、4.6、3.9。运用逐步回归分析功能多样性、功能冗余度与环境参数的关系,结果表明,功能性状多样性指数受总氮、水深影响显著;树状图功能多样性指数受总氮、水深、流速影响显著;功能冗余度指数受硝态氮、溶解氧、二氧化硅影响显著。     

鄂西桑寄生植物多样性的海拔格局

桑寄生植物(桑寄生科)的分布与寄主选择性和生境相关。本研究沿海拔梯度(175～3106 m)设置3条样带共292个样方(20 m×20 m),调查了鄂西亚热带森林群落中桑寄生的分布,记录桑寄生植物多样性。结果表明:在研究区内共调查到7种桑寄生科植物,40种寄主植物;桑寄生植物分布的最低海拔是194 m,最高海拔是2011 m;物种多样性在海拔梯度上先上升后下降,相对集中分布在海拔600～1000 m范围内,呈现单峰分布格局;不同桑寄生科植物在不同寄主植物上的寄生强度不同,更偏好选择高大的落叶乔木作为寄主;桑寄生科植物在鄂西地区海拔梯度上呈"中度膨胀"(mid-elevation peak)的分布格局,可能与寄生植物偏好性及寄主多样性有关。     

西南山地源头溪流附石性水生昆虫群落特征及多样性——以重庆鱼肚河为例

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山西吕梁山草本群落物种多样性的海拔梯度格局及与环境因子的关系

山地草本群落物种多样性的海拔梯度格局及其与环境因子的关系一直是生态学和地理学研究的热点问题。为探究吕梁山草本群落不同尺度物种多样性(α、β、γ多样性)的海拔梯度格局及其与环境因子的关系,该研究采用样方法在吕梁山从北向南选取管涔山、关帝山、五鹿山,并对每个山地划分出高、中、低3个海拔梯度,对草本群落物种多样性和环境因子进行调查分析。结果表明:(1)α多样性随海拔升高呈先升后减的单峰变化格局,峰值出现在中海拔;β多样性中Cody指数在1 900～2 000 m间出现峰值,而BrayCurtis指数出现最小值,表明1 900～2 000 m海拔带是草本群落物种更新速率和组成变化较快的过渡地带;γ多样性随海拔升高也呈先升后减的单峰变化格局(R²=0.406,P<0.01)。(2)海拔对温度、湿度变化的影响极其显著(P<0.01);海拔、温度、湿度等环境因子共同影响物种的α多样性,其中海拔是主要影响因素(P<0.05),温度、湿度影响不显著(P>0.05)。综上所述,吕梁山草本群落多样性在海拔梯度上多表现为"中间膨胀"变化格局,海拔变化是影响多样性变...     

井冈山鹿角杜鹃群落灌木层功能多样性及其随海拔梯度的变化

研究植物群落功能多样性沿环境梯度的变化可以揭示功能多样性与生态系统功能间的关系及维持机制。以井冈山地区鹿角杜鹃（Rhododendron latoucheae）群落为研究对象,通过调查不同海拔梯度群落灌木层植物的物种组成与结构特征,研究了该群落类型灌木层植物的物种多样性、功能多样性、环境因子的特征及其相互之间的关系。结果表明：1）群落类型灌木层植物物种多样性和功能多样性沿海拔梯度呈现不同的变化趋势。物种多样性指数均随着海拔的升高呈减小趋势,而功能多样性指数的变化却较为复杂。其中FRic、FEve和FDis随着海拔的升高显著减小,FDiv和Rao却随海拔的升高而增加;2）群落中物种多样性和功能多样性呈现复杂的相关性。FRic、FEve与丰富度指数呈显著正相关,而Rao、FDis、FDiv与Simpson优势度指数呈线性相关关系,且具有显著相关性;3）群落所分布的坡位及土壤氮与磷含量等环境因子对灌木植物的功能多样性有着重要的影响。鹿角杜鹃群落灌木层植物的物种多样性和功能多样性的相互关系及其对环境变化的响应共同决定了群落的生态系统功能。     

小秦岭森林群落数量分类、排序及多样性垂直格局

采用分层取样的方法,沿小秦岭林区海拔梯度设立56块20 m×20 m样地,用多元回归树(MRT)方法对小秦岭森林群落进行分类,采用除趋势对应分析(DCA)进行排序,用广义可加模型(GAM)研究不同生活型物种多样性沿海拔梯度分布格局。结果表明:(1)56个样地进行MRT分类,经交叉验证并依据植物群落分类和命名原则,本区植物群落可分为5类;(2)样方DCA排序明确地揭示各群落类型生境分布范围,较好地反映小秦岭自然保护区森林群落与环境因子的关系;(3)不同生活型物种多样性指数随海拔梯度变化发生一定的波动,且呈现不同的多样性格局:丰富度指数中,乔木层呈显著的单峰分布格局,灌木层在中海拔段呈明显下降趋势,草本层随着海拔的升高总体呈下降趋势;Shannon-Wiener多样性指数中,不同生活型物种随海拔变化趋势与物种丰富度变化趋势大体相同;不同生活型物种的均匀度指数随海拔变化趋势较平缓。     

Seasonal patterns of taxonomic and functional beta diversity in submerged macrophytes at a fine scale

Spatiotemporal variation in community composition is of considerable interest in ecology. However, few studies have focused on seasonal variation patterns in taxonomic and functional community composition at the fine scale. As such, we conducted seasonal high‐density sampling of the submerged macrophyte community in Hongshan Bay of Erhai Lake in China and used the generalized dissimilarity model (GDM) to evaluate the effects of environmental factors and geographic distance on taxonomic and functional beta diversity as well as corresponding turnover and nestedness components. At the fine scale, taxonomic turnover and nestedness as well as functional turnover and nestedness showed comparable contributions to corresponding taxonomic and functional beta diversity, with different importance across seasons. All taxonomic and functional dissimilarity metrics showed seasonal variation. Of note, taxonomic beta diversity was highest in summer and lowest in winter, while functional beta diversity showed the opposite pattern. Taxonomic and functional turnover showed similar change patterns as taxonomic and functional beta diversity. Taxonomic nestedness was low in summer and high in winter. Functional nestedness was also lower in summer. These results suggest that under extreme environmental conditions, both turnover and nestedness can exist at the fine scale and seasonal community composition patterns in submerged macrophytes should be considered. Future investigations on community assembly mechanisms should pay greater attention to long‐term dynamic characteristics and functional information.     

Invertebrate community responses to land use at a broad spatial scale: trait and taxonomic measures compared in New Zealand rivers

1. Large‐scale comparative studies of ecological responses to anthropological stressors in rivers require measures that are consistent across a range of spatial scales. The biological trait profile of communities offers an alternative approach to traditional measures of macroinvertebrate taxonomic identity and is less constrained by biogeographic influences. 2. We compared the capacities of taxonomic composition and biological trait composition to discriminate the effects of land use (measured as percentage of the catchment in pasture) across a large geographic zone (the whole of New Zealand) in 30 sub‐catchments grouped into five ecoregions throughout the North and South Islands of New Zealand. In addition, we investigated trait consistency (i.e. whether similar traits had similar trait responses to land use at local (catchment) and broad scales). 3. The analysis of taxonomic composition showed that community structure was indeed influenced by land‐use intensity, but that relationships differed among ecoregions. In contrast, traditional assessment metrics (Macroinvertebrate Community Index, richness in Ephemeroptera, Plecoptera and Trichoptera taxa) and trait composition were uninfluenced by region. Trait responses were consistent at the broad and catchment scales, with similar traits responding to pastoral land use at both scales. 4. We used general linear modelling to investigate individual trait responses to land‐use intensity, catchment area and region, focussing on 15 trait categories known to be influenced by land‐use intensity at the catchment scale. Several trait categories varied with land‐use intensity and demonstrated consistency at both catchment and broad scales. Of these, the representation of shorter generation time, asexual reproduction and hermaphroditism, ability to lay eggs beneath the water surface, egg protection and respiration types tolerant of oxygen depletion generally increased in assemblages exposed to more intense pastoral land use. At the same time, the representation of short life duration of adults, prevalence of laying eggs at the water surface, sexual reproduction and low body flexibility decreased in assemblages exposed to land‐use intensification. 5. Our results highlight the value of developing predictive response measures that are relevant at multiple scales and provide the basis for new measures of river condition that are as effective as taxonomic identity in terms of response reliability.     

A macroecological perspective of diversity patterns in the freshwater realm

1. The aim of this paper is to review literature on species diversity patterns of freshwater organisms and underlying mechanisms at large spatial scales. 2. Some freshwater taxa (e.g. dragonflies, fish and frogs) follow the classical latitudinal decline in regional species richness (RSR), supporting the patterns found for major terrestrial and marine organism groups. However, the mechanisms causing this cline in most freshwater taxa are inadequately understood, although research on fish suggests that energy and history are major factors underlying the patterns in total species and endemic species richness. Recent research also suggests that not all freshwater taxa comply with the decline of species richness with latitude (e.g. stoneflies, caddisflies and salamanders), but many taxa show more complex geographical patterns in across‐regions analyses. These complexities are even more profound when studies of global, continental and regional extents are compared. For example, clear latitudinal gradients may be present in regional studies but absent in global studies (e.g. macrophytes). 3. Latitudinal gradients are often especially weak in the across‐ecosystems analyses, which may be attributed to local factors overriding the effects of large‐scale factors on local communities. Nevertheless, local species richness (LSR) is typically linearly related to RSR (suggesting regional effects on local diversity), although saturating relationships have also been found in some occasions (suggesting strong local effects on diversity). Nestedness has often been found to be significant in freshwater studies, yet this pattern is highly variable and generally weak, suggesting also a strong beta diversity component in freshwater systems. 4. Both geographical location and local environmental factors contribute to variation in alpha diversity, nestedness and beta diversity in the freshwater realm, although the relative importance of these two groups of explanatory variables may be contingent on the spatial extent of the study. The mechanisms associated with spatial and environmental control of community structure have also been inferred in a number of studies, and most support has been found for species sorting (possibly because many freshwater studies have species sorting as their starting point), although also dispersal limitation and mass effects may be contributing to the patterns found. 5. The lack of latitudinal gradients in some freshwater taxa begs for further explanations. Such explanations may not be gained for most freshwater taxa in the near future, however, because we lack species‐level information, floristic and faunistic knowledge, and standardised surveys along extensive latitudinal gradients. A challenge for macroecology is thus to use the best possible species‐level information on well‐understood groups (e.g. fish) or use surrogates for species‐level patterns (e.g. families) and then develop hypotheses for further testing in the freshwater realm. An additional research challenge concerns understanding patterns and mechanisms associated with the relationships between alpha, beta and gamma components of species diversity. 6. Understanding the mechanistic basis of species diversity patterns should preferably be based on a combination of large‐scale macroecological and landscape‐scale metacommunity research. Such a research approach will help in elucidating patterns of species diversity across regional and local scales in the freshwater realm.