浮游植物生物量增长模式及抽样、互补效应检验

选取我国近海18种常见浮游植物,以不同物种构建集群,试验研究不同浮游植物集群生物量随物种丰富度的增长模式,运用多因素方差分析检验集群的抽样效应,并分别采用超产分析、相对产量之和分析、子集分析法,检验集群内的生态位互补效应.结果表明:集群生物量随物种丰富度的增长模式不是单一的,当物种数<5时,集群生物量随物种丰富度增加而增大,当物种数>5时,集群生物量与物种丰富度之间无明显规律性;集群内存在较强的互补效应,随物种丰富度的增加呈近似"钟型"曲线变化;集群在生长稳定期存在抽样效应.     

Regional species richness in an obligate subterranean dwelling fauna – epikarst copepods

Aim  The diversity of the obligate cave-dwelling fauna has proved difficult to measure because of the highly localized distributions of most species. We investigated: (1) the local and regional diversity patterns of a major component of the obligate cave-dwelling fauna living in the epikarst zone, the karst layer closest to the surface; (2) variations in local and regional patterns of species richness; and (3) sampling sufficiency at multiple scales.
Location  Caves in the Dinaric Mountains of Slovenia.
Methods  We sampled continuously the abundance of 37 species of copepods dislodged from the epikarst from 35 ceiling drips in six caves for a period of one year. Copepods were collected in a specially designed net that allowed continuous collection.
Results  Based on species accumulation curves and Chao estimates of total diversity, we determined that 3–4 months of continuous sampling were sufficient to find 90% of the species in a drip, that five drips were sufficient to find 90% of the species in a cave, and that five caves were sufficient to find 90% of the species in a region.
Main conclusions  The epikarst copepod fauna is a significant part of the aquatic cave fauna, contributing about 20% at the regional level. Because of the scale of variation, much of which occurs within a cave, and because of the availability of continuous sampling devices, the epikarst component of subterranean diversity seems to be more thoroughly and accurately measured than do other components.     

Evaluating the performance of species richness estimators: sensitivity to sample grain size

1. Fifteen species richness estimators (three asymptotic based on species accumulation curves, 11 nonparametric, and one based in the species-area relationship) were compared by examining their performance in estimating the total species richness of epigean arthropods in the Azorean Laurisilva forests. Data obtained with standardized sampling of 78 transects in natural forest remnants of five islands were aggregated in seven different grains (i.e. ways of defining a single sample): islands, natural areas, transects, pairs of traps, traps, database records and individuals to assess the effect of using different sampling units on species richness estimations. 2. Estimated species richness scores depended both on the estimator considered and on the grain size used to aggregate data. However, several estimators (ACE, Chao 1, Jackknifel and 2 and Bootstrap) were precise in spite of grain variations. Weibull and several recent estimators [proposed by Rosenzweig et al. (Conservation Biology, 2003, 17, 864-874), and Ugland et al. (Journal of Animal Ecology, 2003, 72, 888-897)] performed poorly. 3. Estimations developed using the smaller grain sizes (pair of traps, traps, records and individuals) presented similar scores in a number of estimators (the above-mentioned plus ICE, Chao2, Michaelis-Menten, Negative Exponential and Clench). The estimations from those four sample sizes were also highly correlated. 4. Contrary to other studies, we conclude that most species richness estimators may be useful in biodiversity studies. Owing to their inherent formulas, several nonparametric and asymptotic estimators present insensitivity to differences in the way the samples are aggregated. Thus, they could be used to compare species richness scores obtained from different sampling strategies. Our results also point out that species richness estimations coming from small grain sizes can be directly compared and other estimators could give more precise results in those cases. We propose a decision framework based on our results and on the literature to assess which estimator should be used to compare species richness scores of different sites, depending on the grain size of the original data, and of the kind of data available (species occurrence or abundance data).     

Changes of species richness pattern in mountain grasslands: abandonment versus restoration

Changes in plant species richness at various spatial scales were investigated by manipulative experiment in mountain grasslands. The aim of the research was to compare changes in species richness in newly abandoned sites and sites where restoration measures were applied after 20 years of abandonment. The plots were located in two vegetation types with different moisture regime. Species richness decreased significantly after abandonment, mainly at the finest spatial scale of 10 × 10 cm. There was significant increase of species richness on restored sites, but it was apparent mainly at a larger scale. However, even 4 years of regular mowing were not sufficient to restore species richness to the level typical for traditionally managed grasslands in the region. No significant difference was found in the performance of the 2 contrasting vegetation types (wet and dry) in relation to management measures. A significant difference in scale-dependent species richness was only observed. The dry type had a steeper species-area curve, with a lower number of species at the finest spatial scale. According to the results of the experiment, mountain grasslands are very vulnerable habitats, losing their conservation value quickly after abandonment. Restoration is possible due to an extensive species pool in the region, but return to the original species richness at all spatial scales is quite a long process.     

Hotspots and richness pattern of grasshopper species in cultural landscapes

The success of the hotspot approach for biodiversity conservation depends on the spatial scale and the indicator species used. In this study, we investigated grasshopper species richness in Switzerland at a 1 ha resolution including a total of 111 species. We compared the representativeness of common and of endangered grasshopper species for the overall grasshopper species richness and we assessed the efficiency of the hotspot approach for grasshopper conservation. The pattern of overall grasshopper species richness was well represented by both the number of common and the number of endangered grasshopper species. For evaluating the efficiency of different hotspot approaches for conservation, we compared hotspots of common species, hotspots of endangered species (rarity hotspots), and hotspots of all grasshopper species (richness hotspots). Among these hotspot types, richness hotspots not only featured most common grasshopper species, but they even contained more endangered species than the rarity hotspots. The combination of rarity hotspots and hotspots of common species featured more species than the other combinations of hotspot types. However, the gain of combining two hotspot types compared to the single-hotspot approach was low (max. 3 species). About 24% of the species were not contained in any of the hotspots. These grasshopper species require species-specific action plans. As rarity hotspots were located in areas that are rather strongly affected by landscape change, species richness in rarity hotspots may decrease in the future. We conclude that, for grasshoppers, the hotspot approach on the 1 ha scale can be an effective way to conserve a high proportion of species richness.     

Climate-based model of spatial pattern of the species richness of ants in Georgia

For optimal planning of conservation and monitoring measures, it is important to know the spatial pattern of species richness and especially areas with high species richness. A spatial pattern of the species richness of ants in Georgia (Caucasus) was modeled, areas with the highest number of ant’s species were inferred, and climatic factors that influence the pattern of ant diversity were identified. A database was created by accumulating occurrences for 63 ant species, including 256 localities and 2,018 species/occurrences. Species richness was positively correlated with variables associated with temperature and negatively correlated with variables associated with precipitation. Species richness reaches a maximum at the elevations 800–1,200?m a.s.l. and declines at both lower and higher altitudes. The role of climatic variables and geography of the study area in determining the observed pattern of species richness is discussed.     

二道白河河岸带植物群落最小面积与物种丰富度

河岸带是森林小流域单元的重要组成部分之一。由于河水的影响和边缘效应等因素的综合作用,河岸带植物群落与远离河岸带的森林群落在组成,结构和分布格局等方面存在较大差异,其如落最小面积也不同。本文对长白山原始阔叶红松林河岸带植物群落最小面积和物种丰富度进行了探讨。结果表明,河岸带植物群落的最小面积均小于远离河岸带的森林群落的最小面积,在河岸带,阔叶红松林群落的60,80和90％植物在时的平均最小面积分别约为80,180和320m^2;而远离河岸带的森林内部,相应的平均最小面积分别为260,380和480m^2左右。河岸带植物群落的物种丰富度普遍高于森林群落。     

Assessing bee species richness in two Mediterranean communities: importance of habitat type and sampling techniques

The decline of bees has raised concerns regarding their conservation and the maintenance of ecosystem services they provide to bee-pollinated wild flowers and crops. Although the Mediterranean region is a hotspot for bee species richness, their status remains poorly studied. There is an urgent need for cost-effective, reliable, and unbiased sampling methods that give good bee species richness estimates. This study aims: (a) to assess bee species richness in two common Mediterranean habitat types: semi-natural scrub (phrygana) and managed olive groves; (b) to compare species richness in those systems to that of other biogeographic regions, and (c) to assess whether six different sampling methods (pan traps, variable and standardized transect walks, observation plots and trap nests), previously tested in other European biogeographic regions, are suitable in Mediterranean communities. Eight study sites, four per habitat type, were selected on the island of Lesvos, Greece. The species richness observed was high compared to other habitat types worldwide for which comparable data exist. Pan traps collected the highest proportion of the total bee species richness across all methods at the scale of a study site. Variable and standardized transect walks detected the highest total richness over all eight study sites. Trap nests and observation plots detected only a limited fraction of the bee species richness. To assess the total bee species richness in bee diversity hotspots, such as the studied habitats, we suggest a combination of transect walks conducted by trained bee collectors and pan trap sampling.     

Changes in the species richness,spatial pattern and species frequency associated with the decline of oak forest

Nomenclature: follows Flora Europea (Tutin et al. 1964–1980). Since the extension of the irrigation system, the water regime of most of the permanent marshes of the Camargue (southern France) have been intensively controlled. Considerable quantities of nutrient rich Rhone water are pumped into these marshes, leading to lower salinities and a higher biomass production and consequently an increasing organic matter concentration of the sediments. Myriophyllum spicatum has become abundant in these permanent marshes since large quantities of freshwater entered these systems. It has displaced Potamogeton pectinatus in several of these marshes. The different factors likely to influence the distribution of P. pectinatus and M. spicatum were investigated experimentally. The impact of Cl^- concentrations between 0 and 6 g l^-1 on the biomass production of both species was tested. P. pectinatus appears to be more salt tolerant than M. spicatum. The influence of sediment quality on the biomass production of both species was investigated using six sediments differing in organic matter concentration. Compared to P. pectinatus, M. spicatum had a lower total biomass production when grown on sediments with low organic matter concentration (2–4% organic matter) and a higher biomass production on sediments with relatively high organic matter concentration (9–13% organic matter).Nitrogen addition to the sediments yielded an increased biomass production of P. pectinatus and M. spicatum. On some sediments M. spicatum needed higher concentrations of nitrogen than P. pectinatus to increase its biomass production.The creation of freshwater marshes by the introduction of irrigation water, resulting in lower salinities and an increase in sediment organic matter concentration, stimulates the biomass production of M. spicatum.As M. spicatum grows less well on poor sediments and at higher salinities it seems to be unable to displace P. pectinatus in more natural systems in the Camargue.     

The relationship between percentage of singletons and sampling effort: A new approach to reduce the bias of richness estimates

Estimate the richness of a community with accuracy despite differences in sampling effort is a key aspect to monitoring high diverse ecosystems. We compiled a worldwide multitaxa database, comprising 185 communities, in order to study the relationship between the percentage of species represented by one individual (singletons) and the intensity of sampling (number of individuals divided by the number of species sampled). The database was used to empirically adjust a correction factor to improve the performance of non-parametrical estimators under conditions of low sampling effort. The correction factor was tested on seven estimators (Chao1, Chao2, Jack1, Jack2, ACE, ICE and Bootstrap). The correction factor was able to reduce the bias of all estimators tested under conditions of undersampling, while converging to the original uncorrected values at higher intensities. Our findings led us to recommend the threshold of 20 individuals/species, or less than 21% of singletons, as a minimum sampling effort to produce reliable richness estimates of high diverse ecosystems using corrected non-parametric estimators. This threshold rise for 50 individuals/species if non-corrected estimators are used which implies in an economy of 60% of sampling effort if the correction factor is used.     

Latitudinal patterns of mammalian species richness in the New World: the effects of sampling method and faunal group

Abstract. Although the latitudinal gradient of species richness for mammals in North America is well documented, few investigators have quantified the relationship in South America. We examined the pattern in North and South America, at two spatial scales (2.5° and 5°) for each of two sampling methods (quadrats and latitudinal bands). A scale effect was evident for quadrats but not for bands. Significant linear relationships between species richness and latitude were found for three faunal groups: all mammals, nonvolant species, and bats. Effects of area confound the latitudinal relationship. By statistically removing such effects, we found that the latitudinal gradient is not an artifact of the species-area relationship, and that the latitudinal gradients for North and South America were statistically indistinguishable. Our data suggest that both faunal subgroups, nonvolant species and bats, contributed substantially to the overall mammalian pattern. Further, multiple regression analyses showed that only latitude is a necessary variable to explain bat richness; for nonvolant species, in addition to latitude, area and longitude may be important.     

国裸子植物物种丰富度空间格局与多样性中心

中国拥有世界上最丰富的裸子植物区系,对理解全球裸子植物分布变化与系统演化具有重要意义.我们利用中国天然分布的202种裸子植物的水平和垂直分布信息获得物种分布区范围,探讨了中国裸子植物在科、属、种水平的分布特点.总体上,中国裸子植物物种丰富度南高北低,山地裸子植物丰富度较高,平原和高原相对贫乏;随分类阶元变高,丰富度高值区域面积逐渐扩大,高值中心逐渐南移.占中国陆地面积5%的裸子植物最丰富区域内分布了85%的中国自然分布的裸子植物物种.我们将这些区域划分为6个裸子植物多样性中心:(1)东喜马拉雅-横断山脉-秦岭,(2)滇黔桂-南岭,(3)华中山地,(4)黄山-武夷山脉,(5)海南岛南部山地,(6)长白山(甑峰山附近).各中心裸子植物区系之间的特点和联系反映了各自地理位置的差异和空间距离的隔离作用,其中横断山脉地区是中国裸子植物最重要的分化中心.     

The influence of trap density and sampling duration on the detection of small mammal species richness

Assessing species richness of small mammal communities is an important research objective for many live-trapping studies designed to assess or monitor biological diversity. We tested the effectiveness and efficiency of various trap densities for determining estimates and counts of small mammal species richness. Trapping was conducted in grassland habitats in northeastern Kansas during spring and fall of 2002 and 2003. Estimates and counts of species richness were higher at increased trap densities. This effect appeared to be primarily due to the higher number of individuals sampled at higher trap densities. At least 3 nights duration was needed to produce a stable estimate of species richness for the range of trap densities tested (9–144 trap stations/ha). Higher trap densities generally reached stable richness estimates in fewer nights than low density trapping arrangements. Given that counts and estimates of species richness were influenced by trap density and sampling duration, it is critical that these parameters are selected to most effectively meet research objectives.     

The contribution of common and rare species to plant species richness patterns: the effect of habitat type and size of sampling unit

Understanding how overall patterns of spatial variation in species richness are affected by distributional patterns of species has been an area of growing concern. In the present study, we investigated the relative importance of common and rare species as contributors in overall plant species richness. We further examined if the effects of common or rare species in richness patterns are affected by the size of the sampling units and if the observed patterns hold at different habitats. We used a dataset of 5,148 higher plant species distributed across 16,114 sampling plots located in 240 sites of the NATURA 2000 network of Greece. We ranked all species based on the number of sites they occupied and we developed a common to rare and a rare to common sequence. We correlated those sequences with cumulative species distributions. We performed this analysis in nine different sizes of sampling units and in three different datasets referring to (a) all habitat types together, (b) coniferous habitats only and (c) alpine habitats only. Our analysis showed that despite the proportionally higher numbers of restricted species, widespread species make a greater contribution to overall richness patterns and that this observed pattern does not depend on the size of the sampling units. Moreover, the observed pattern stands for different habitat types. Our findings support the generality of this pattern and highlight the importance of widespread species as adequate indicators of biodiversity patterns at various habitat types. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

The importance of plot size and the number of sampling seasons on capturing macrofungal species richness

The species-area relationship is an important factor in the study of species diversity, conservation biology, and landscape ecology. A deeper understanding of this relationship is necessary, in order to provide recommendations on how to improve the quality of data collection on macrofungal diversity in different land use systems in future studies, a systematic assessment of methodological parameters, in particular optimal plot sizes. The species-area relationship of macrofungi in tropical and temperate climatic zones and four different land use systems were investigated by determining the macrofungal species richness in plot sizes ranging from 100 m² to 10 000 m² over two sampling seasons. We found that the effect of plot size on recorded species richness significantly differed between land use systems with the exception of monoculture systems. For both climate zones, land use system needs to be considered when determining optimal plot size. Using an optimal plot size was more important than temporal replication (over two sampling seasons) in accurately recording species richness.     

Effect of sampling pattern on estimation of species distributions along gradients

Computer simulation and statistical theory indicate that estimation of species distribution is difficult when species reach maximum abundance near one end of the sampled portion of a gradient or when they have wide ecological breadth. Relative to balanced sampling of the whole gradient, concentration of sampling effort near the ends increases accuracy in estimation of distributions of truncated species more than it decreases accuracy for other species. Hence, overall accuracy in the estimation of distributions for a collection of species with modes scattered about on a gradient is greatest when sampling is somewhat more intense near the extremes of the gradient.