Current Species Richness Research Articles

The effects of extreme forest fragmentation on the bird community of Singapore Island

Singapore Island suffered one of the highest known deforestation rates in the tropics from the mid-to-late 19th century when over 95% of its native lowland forest was cleared. We compared the current bird community structure and composition among three habitat types, i.e., old (>50 years, 7–935 ha) and young (⩽50 years, 29–49 ha) naturally regenerating secondary forests and abandoned wooded plantations (27–102 ha) dominated by exotic species. Forest patch area had the strongest influence on the current species richness. The overall bird richness was not greater in most mature forest patches, but 20 species were only found in the old secondary forests and five of these were found in <50% of these patches. The rapid decrease in the number of forest species in plantations was offset by an increase in the number of open habitat species. Comparisons with current bird communities in nearby mainland forest sites (Peninsular Malaysia) suggest that the forest avifauna of Singapore is depauperate. The preservation of larger mature and maturing forests is therefore required for conserving the extant forest avifauna in Singapore. Connecting isolated patches can also be envisioned to facilitate movements of forest birds that have low densities and restricted distribution.

Estimation and prediction of plant species richness in a mosaic landscape

Traditional agricultural mosaic landscapes are likely to undergo dramatic changes through either intensification or abandonment of land use. Both developmental trends may negatively affect the vascular plant species richness of such landscapes. Therefore, sustainable land-use systems need to be developed to maintain and re-establish species richness at various spatial scales. To evaluate the sustainability of specific land-use systems, we need approaches for the effective assessment of the present species richness and models that can predict the effects on species richness as realistically as possible. In this context, we present a methodology to estimate and predict vascular plant species richness at the local and the regional scale. In our approach, the major determinants of vascular plant species richness within the study area are taken into consideration: These are according to Duelli's mosaic concept the number of habitat types and of habitat patches within area units. Furthermore, it is based on the relative frequencies of species within habitat types. Our approach comprises six steps: (i) the determination of present habitat patterns within an observation area, (ii) the creation of a land-use scenario with simulated habitat patterns, (iii) the determination of species frequencies within habitat types of this area, (iv) a grouping of habitat-specific species, (v) the estimation of the probabilities for all species (or habitat specialists) to occur, either in stepwise, exponentially enlarged landscape tracts (local scale), or in the entire observation area (regional scale), and (vi) the validation of the estimated species numbers. The approach will be exemplified using data from the municipal district of Erda, Lahn-Dill Highlands, Germany. The current species numbers to be expected on the basis of probability calculations were compared with those recorded on the basis of extensive field work. This comparison shows that, on the basis of our simple calculations, the current local plant species richness can be predicted well, with a slight underestimation.

A tale of two analyses: estimating the consequences of shifts in hexapod diversification

I present a novel descriptive (non-statistical) method to help identify the location and importance of shifts in diversification across a phylogeny. The method first estimates radiation rates across terminal higher taxa and then subjects these rates to a parsimony analysis across the phylogeny. The reconstructions define the magnitude, direction and influence of past shifts in realized diversification rates across nodes. I apply the method to data on the extant hexapod orders. The results indicate that the Coleoptera (beetles) and Diptera (flies) have contributed large upward shifts in diversification tendency, without which, under the model employed, global species richness would be reduced by 20% and 6%, respectively. The origin of Neoptera (insects with wing flexion), identified elsewhere as a significant radiation, may represent a large positive, a large negative or zero influence on current species richness, depending on the assumed phylogeny and parsimony method. The most influential radiations are attributable to the origin of the Eumetabola (insects with complete metamorphosis plus bugs and their relatives) and Pterygota (winged insects), but there is presently only weak evidence that they represent significant shifts in underlying diversification tendency. These analyses support some but not all results of previous phylogenetic analyses and the identity of the most important shift therefore remains elusive. New methodology involving comparisons across multiple taxa is likely to be necessary. © 2003 The Linnean Society of London, Biological Journal of the Linnean Society, 2003, 80, 23–36.

Effects of errors in range maps on estimates of historical species richness of mammals in Canadian national parks

AbstractAim Tests for faunal relaxation in reserves, particularly for mammals, have relied on comparisons of current species richness with estimates of species richness derived from historical range maps. However, any range map reflects the extent of occurrence of species and not necessarily the area of occupancy. Thus, estimates of historical species richness might be prone to error introduced by ‘false positives’, that is, a species might be considered to have been present in locations where it actually was not. The effect of such ‘false positives’ could bias statistical tests of faunal relaxation to type I error, and result in estimates of the extent of faunal relaxation in reserves greater than was actually the case. We evaluated the potential for errors in historical range maps to generate inflated estimates of historical species richness of mammals at sites that are reserves today.Location Canadian national parks in the Canadian portion of the Alleghenian‐‐Illinoian mammal province in south‐eastern Canada (the maritime region and parts of southern Québec, Ontario and Manitoba).Methods The effect of varying levels of error in range maps on estimates of historical species richness was tested using geographical information systems (GIS)‐based statistical sampling of simulated historical ranges. Species’ areas of occupancy were simulated to be only 25%, 75% and 95% of published historical species ranges. For each reserve, estimates of historical species richness from these simulated species ranges were then compared with similar, previously published estimates of richness based on published historical species ranges.Results Previous estimates of historical species richness for reserves were inversely and linearly related to the degree of inaccuracy of species ranges. If species ranges were, on average, 5% smaller than the accepted ranges, then estimates of historical species richness agreed with previous estimates in c. 90% of cases. However, if historical ranges were, on average, 25% smaller than those used in previous analyses, then previous historical estimates of species richness may be overestimates in c. 40% of cases.Main conclusions Estimates of the extent of faunal relaxation in reserves that use historical range maps to quantify past species richness appear to be sensitive to even small errors in the degree to which range maps may overestimate ‘area of occupancy’.

Plant communities of field boundaries in Finnish farmland

To determine the importance of field boundary habitats for farmland biodiversity, we surveyed a total of 193 boundaries from four climatically and agriculturally dissimilar regions in Finland. We measured the current plant species richness and composition of the boundaries, and based on the differences in vegetation characteristics, we describe six boundary types. The observed plant species were mainly indicators of fresh to wet soils and moderate to rich mineral nitrogen content. The most frequent species were tall, perennial monocots and dicots indicating the high productivity of thevegetation. Moreove, herbicide-tolerant species were common. No species rare for Finland were found.In animal husbandry regions, the most frequent species were sown grassland species and typical grassland weeds. In cereal production regions, fast-spreading root weeds tolerant of herbicides were the most frequent. Mean species richness was highest in the cluster Ca-lamagrostis-Phalaris (24 species (s)/boundary (b)), which we considered as representative of moist sites with some disturbance by agricultural practices. Most species-poor were the clusters Elymus-Anthriscus (14 s/b)and Elymus-Cirsium (16 s/b),both found predominantly in cereal production regions in southern Finland. Our results suggest that the biodiversity value of boundaries is lowest in the most intensive cereal production areas and highest in areas of mixed farming.;

Conservation of Mammals in Eastern North American Wildlife Reserves: How Small Is Too Small?

Abstract: A common objective of methods of systematic reserve selection has been to maximize conservation benefits—frequently current species richness—while reducing the costs of acquiring and maintaining reserves. But the probability that a reserve will lose species in the future is frequently not known because the minimum area requirements for most species have not been estimated empirically. For reserves within the Alleghenian‐Illinoian mammal province of eastern North America, we empirically estimated the minimum area requirement of terrestrial mammals such that reserves should not lose species because of insularization. We compared this estimate to the actual size of 2355 reserves and reserve assemblages within the mammal province. The estimated minimum area requirement was 5037 km2 (95% CI: 2700–13,296 km2). Fourteen reserves and reserve assemblages were&gt; 2700 km2, 9 were&gt; 5037 km2, and 3 were&gt; 13,296 km2. These 14 reserves accounted for 73% of the total area of reserves and 10% of the total area of the mammal province. Few reserves appear large enough to avoid loss of some mammal species without the additional cost of active management of habitat or populations. Immigration corridors and buffer zones that combine small reserves into assemblages totaling at least 2700 km2 may be the most efficient means of conserving mammals in these reserves.

Insular biogeography of mammals in Canadian parks: a re‐analysis

Summary Aim Glenn &amp; Nudds (1989) compared mammal species richness in Canadian parks to estimated species‐area relationships prior to European settlement to test if parks presently contain their historical compliment of species. However, the data they used to estimate the presettlement species‐area relationships were not commensurate with the scale of the parks and were not independent. This uncertainty reduces the utility of Glenn and Nudds analysis to detect which, if any, parks are experiencing mammal extirpations and ultimately to direct conservation efforts to enhance mammal conservation in Canada. We improved Glenn and Nudds methods and re‐assesed the conservation status of mammals in Canadian parks. Location Canada. Methods We constructed species‐area curves for disturbance tolerant and intolerant species in five mammal regions of Canada by sampling historical range maps using plots of 10– 10,000 km2. We compared these estimates of expected species richness to current species richness in thirty‐six parks and contrast our results with those of Glenn and Nudds. Results All ten re‐estimated species‐area regressions had higher intercepts than those reported by Glenn and Nudds; four had lower slopes. Of seventy‐two cases analysed, we found twenty in which parks had fewer species than expected and four in which parks had more species than expected, compared to fourteen and thirty‐three, respectively, reported by Glenn and Nudds. Changes in both the regression parameters and increases in the prediction intervals accounted for the disparity between these results. Park residuals were not significantly different from zero in eight of ten analyses. Residuals for parks in the Alleghenian‐Illinoian mammal province were negative and decreased with increasing park size. Main conclusions Improvement of Glenn and Nudds methods had an effect on both the parameter estimates and precison of the presettlement species‐area curves. As a result, mammal conservation in some Canadian parks is worse than Glenn and Nudds reported. Six additional parks contained fewer disturbance intolerant species than predicted. However, Glenn and Nudds finding of systematic differences between expected and observed species richness in parks in the densely populated region of southern Ontario, southern Quebec and the maritime provinces was not an artefact of their methods. In this region, seven of ten parks appear to have lost disturbance‐sensitive species of mammals. The pattern of species loss in this region was consistent with the idea that these parks have become isolated from mammal dispersal by surrounding habitat change and have experienced local species extirpations.

Importance of historical factors on species richness and composition of butterfly assemblages (Lepidoptera: Rhopalocera) in a northern Iberian mountain range

ABSTRACT. The butterfly assemblages of three vegetation types (pasture, heathland and rocky outcrop with Genista spp.) and two geographical orientations (a northern slope and a sheltered gorge) were studied along an altitudinal gradient in the Picos de Europa in northern Spain. In order to study the effects or historical climatic changes on current butterfly assemblages, it was examined if changes in richness and faunal composition of assemblages were joined with changes in their biogeographical composition. The three vegetation types showed characteristic butterfly assemblages, but no difference in species richness and biogeographical composition was found. Species richness in the sheltered gorge was higher than in the northern slope. Faunal composition also varied between orientations and there were more widespread and Mediterranean species in the sheltered gorge than in the northern slope. Species richness declined with increasing altitude, though a midaltitudinal peak was observed. There was a faunal segregation between high and low localities. Species richness of widespread and Mediterranean butterflies decreased as altitude increased, whereas the reverse was true for montane species. Moreover, biogeographical elements differed in their climatic tolerances measured as altitudinal ranges. Therefore, changes in richness and composition of butterfly assemblages between both slopes and along the altitudinal gradient were joined in part with variation in their biogeographical composition. These results suggest that current species richness and composition of butterfly assemblages in the Picos de Europa might be the consequence of differential colonization of refuges during the past climatic changes.

Specialization of Phytophagous Arthropod Communities on Introduced Plants

Arthropod herbivore communities vary in the proportion of plant family specialists and broad generalists. Examination of the literature of 23 annual crop plant species and the associated feeding relations of 498 arthropod species in Japan revealed that contemporary cropping area was only weakly associated with current arthropod species richness and that the proportion of plant family specialists was greater and the proportion of generalists was lower on plant species that had been in Japan for longer periods of time. These results suggest that arthropod communities become increasingly more specialized or less generalized the longer a plant coexists with the community, and that this process can occur over time periods of a few thousand years. Exotic arthropod species associated with these plants and known to have invaded Japan in the last 100—200 yr are more generalized than the native fauna, so species invasions could not contribute to the increased specialization or decreased generalization with time.