Annual respiration and production estimates for collembolan and psocopteran epiphyte herbivores on larch trees in southern England

ABSTRACT.

• 1 The population and biomass dynamics of the collembolan and psocopteran epiphyte herbivores on larch trees at Ranmore Common, Surrey, were followed from October 1976 to October 1978.
• 2 The effect of temperature and body weight on the metabolic rate of the epiphyte herbivores was determined in the laboratory.
• 3 The metabolic rate of Psocoptera appears little influenced by changes in temperature within the range they normally experience in the field. This‘low Q₁₀ metabolism’is discussed in the light of other studies of species showing a similar phenomenon.
• 4 The collembolan metabolism also shows some temperature compensation.
• 5 The laboratory studies on metabolic rate are combined with field data to give annual respiration and production estimates.
• 6 The data from southern England are compared with published data from northern England sites and their differences discussed.

     

A study of species richness and diversity in seed banks and its use for the environmental mitigation of a proposed holiday village development in a coniferized woodland in south east England

A survey was carried out to determine the density and species composition of germinable seed in the surface soil layers of 30 plots within a coniferized lowland woodland in East Kent in order to establish the resources available for habitat creation in the event of some areas being modified during a proposed holiday village development. The selected plots included conifer plantations (up to 69 years old), broad-leaved plantations and the semi-natural broad-leaved edges that remain on parts of the perimeter of the site which were used as the control. A total of 13 682 seedlings emerged from the soil samples during the four-month germination trials. Fifty-two species were identified of which eight were ancient woodland indicator species for south-east England. The most abundant species represented in the seed banks were: Juncus effusus, Rubus fruticosus, Carex sylvatica, Betula pendula and Agrostis tenuis. Between-site comparisons of coniferous plots of different ages revealed a marked reduction in the seed species and seed density in plantations over 65 years old. Results of soil nutrient and texture analyses ruled out the likelihood of edaphic factors being responsible for between-site differences in seed bank composition. Seed species richness and diversity (Shannon-Wiener diversity index) were greatest in the semi-natural broad-leaved edges, but the diversity index used also showed that two replanted conifer sites had high values despite few species being present. The usefulness and limitations of diversity indices in the context of seed bank studies is discussed. From the results of the study, management proposals for the site have been put forward in order to maintain floristic diversity and mitigate the impact of the proposed development.     

Bird species richness and densities in relation to sulphur dioxide gradients and environmental variables

The expansion of coal-fired power stations in South Africa has resulted in growing environmental concerns as they are the largest emitters of sulphur dioxide (SO₂). Sulphur dioxide emissions from power plants pose a potential threat to avian populations. However, the effect of SO₂ pollution on bird communities is poorly understood. Using point counts we investigated the relationships of bird species richness and species-specific density with SO₂ concentrations around Matimba power station. Environmental parameters were derived from remotely sensed data and data reduction was performed using principal component analysis. Generalised linear mixed models were then used to infer the relationships of bird species richness and species-specific densities with SO₂ concentrations and the environmental variables. Our results revealed that SO₂-polluted air had no influence on bird species richness and densities in our study sites, but SO₂ levels were below annual national ambient air quality standards. Vegetation productivity was found to have a greater influence on species densities than SO₂ pollution. Monitoring of bird population changes around Matimba power station once neighbouring Medupi power station is fully operational is recommended, as SO₂ content of the air will increase significantly, and species may be sensitive to this increase in SO₂ levels.     

Archaeobotanical evidence for climate as a driver of ecological community change across the anthropocene boundary

The biodiversity response to climate change is a major focus in conservation research and policy. Predictive models that are used to project the impact of climate change scenarios – such as bioclimatic envelope models – are widely applied and have come under severe scrutiny. Criticisms of such models have focussed on at least two problems. First, there is an assumption that climate is the primary driver of observed species distributions (‘climatic equilibrium’), when other biogeographical controls are often reliably established. Second, a species' sensitivity to macroclimate may become less relevant when impacts are down‐scaled to a local level, incorporating a modifying effect of species interactions structuring communities. This article examines the role of different drivers (climate, pollution and landscape habitat structure) in explaining spatial community variation for a widely applied bioindicator group: lichen epiphytes. To provide an analysis free of ‘legacy effects’ (e.g. formerly higher pollution loads), the study focused on hazel stems as a relatively short‐lived and recently colonized substratum. For communities during the present day, climate is shown to interact with stem size/age as the most likely explanation of community composition, thus coupling a macroclimatic and community‐scale effect. The position of present‐day communities was projected into ordination space for eight sites in England and compared to the position of historical epiphyte communities from the same sites, reconstructed using preserved hazel wattles dating mainly to the 16th Century. This comparison of community structure for the late‐ to post‐Mediaeval period, with the post‐Industrial period, demonstrated a consistent shift among independent sites towards warmer and drier conditions, concurrent with the end of the Little Ice Age. Long‐term temporal sensitivity of epiphyte communities to climate variation thus complements spatial community patterns. If more widely applied, preserved lichen epiphytes have potential to generate new baseline conditions of environment and biodiversity for preindustrial lowland Europe.     

Eutrophication,biodiversity loss,and species invasions modify the relationship between host and parasite richness during host community assembly

Host and parasite richness are generally positively correlated, but the stability of this relationship in response to global change remains poorly understood. Rapidly changing biotic and abiotic conditions can alter host community assembly, which in turn, can alter parasite transmission. Consequently, if the relationship between host and parasite richness is sensitive to parasite transmission, then changes in host composition under various global change scenarios could strengthen or weaken the relationship between host and parasite richness. To test the hypothesis that host community assembly can alter the relationship between host and parasite richness in response to global change, we experimentally crossed host diversity (biodiversity loss) and resource supply to hosts (eutrophication), then allowed communities to assemble. As previously shown, initial host diversity and resource supply determined the trajectory of host community assembly, altering post‐assembly host species richness, richness‐independent host phylogenetic diversity, and colonization by exotic host species. Overall, host richness predicted parasite richness, and as predicted, this effect was moderated by exotic abundance—communities dominated by exotic species exhibited a stronger positive relationship between post‐assembly host and parasite richness. Ultimately, these results suggest that, by modulating parasite transmission, community assembly can modify the relationship between host and parasite richness. These results thus provide a novel mechanism to explain how global environmental change can generate contingencies in a fundamental ecological relationship—the positive relationship between host and parasite richness.     

Niche conservatism and species richness patterns of squamate reptiles in eastern and southern Africa

Niche conservatism has been proposed as a mechanism influencing large‐scale patterns of taxonomic richness. We document the species richness patterns of five monophyletic squamate reptile groups (gekkonids, cordylids‐scincids, lacertids, chameleons and alethinophidian snakes) in eastern and southern Africa, and explore if observed patterns reflect niche conservatism processes. We quantified richness and its relationships with current climatic conditions by gridding species' range maps at 110 × 110 km. Also, dated phylogenies and palaeoclimatic reconstructions, coupled with evidence from the fossil record, were used to approximate the areas and climate characteristics in which each group originated and/or radiated. Mean species richness and geographically corrected confidence intervals in current climate types were calculated for each group in order to establish their climatic preferences. On average, the species richness of older groups (gekkonids, cordylids‐scincids and lacertids) was lower in equatorial climates and higher in arid and temperate conditions, whereas more recent groups (chameleons and alethinophidian snakes) were richer in equatorial and temperate climates and less rich in arid conditions. Across all groups, higher richness was associated with climatic characteristics similar to those prevailing at the time in which each group originated/radiated. The congruence of the current climates where reptile groups are richer and the past climates amidst which those groups originated is consistent with an explanation for their diversity gradients based on niche conservatism.     

Changes in species richness of vascular plants under the impact of air pollution: a global perspective

Aim To investigate the general pattern of changes in species richness and diversity of vascular plants due to environmental contamination and associated habitat changes imposed by point polluters, and identify the sources of variation in the response of plant communities to industrial pollution. Location Global. Methods We collected species richness and diversity data from 86 studies that were conducted around 60 atmospheric point polluters worldwide and reported in 95 papers (published in 1953–2007). We used meta‐analysis to search for a general effect and to compare between polluter types and plant groups, and linear regression to describe the latitudinal gradient and to quantify relationships between pollution and effect size. Results Although the species richness of vascular plants generally decreased with pollution, the effects were not uniform across the studies. Polluters that cause soil acidification imposed a stronger detrimental effect on plant diversity than industries whose emissions increased soil pH. An overall adverse effect was primarily due to the contribution of non‐ferrous smelters and aluminium plants; the effects of other SO₂‐emitting industries were less detrimental, albeit negative, and the effects of chemical plants, fertilizer factories and cement industries did not differ from zero. Longevity of the pollution impact only made a slight contribution to the detected variation, while adverse effects increased with increase in pollution load. Main conclusions This study is the first demonstration of geographical variation in the responses of plant communities to aerial emissions: adverse effects increased from high to low latitudes, and this pattern was explained primarily by increases in both the diversity of original (undisturbed) communities and mean summer temperatures. The latter result suggests that under a future warmer climate the existing pollution loads may become more harmful. Model calculations indicate that a detectable depauperation of plant communities is unlikely if the polluter emits < 1500 t of SO₂ annually.     

Ancient DNA evidence for the loss of a highly divergent brown bear clade during historical times

The genetic diversity of present-day brown bears (Ursus arctos) has been extensively studied over the years and appears to be geographically structured into five main clades. The question of the past diversity of the species has been recently addressed by ancient DNA studies that concluded to a relative genetic stability over the last 35,000 years. However, the post-last glacial maximum genetic diversity of the species still remains poorly documented, notably in the Old World. Here, we analyse Atlas brown bears, which became extinct during the Holocene period. A divergent brown bear mitochondrial DNA lineage not present in any of the previously studied modern or ancient bear samples was uncovered, suggesting that the diversity of U. arctos was larger in the past than it is now. Specifically, a significant portion (with respect to sequence divergence) of the intraspecific diversity of the brown bear was lost with the extinction of the Atlas brown bear after the Pleistocene/Holocene transition.     

Genetic diversity loss in a biodiversity hotspot: ancient DNA quantifies genetic decline and former connectivity in a critically endangered marsupial

The extent of genetic diversity loss and former connectivity between fragmented populations are often unknown factors when studying endangered species. While genetic techniques are commonly applied in extant populations to assess temporal and spatial demographic changes, it is no substitute for directly measuring past diversity using ancient DNA (aDNA). We analysed both mitochondrial DNA (mtDNA) and nuclear microsatellite loci from 64 historical fossil and skin samples of the critically endangered Western Australian woylie (Bettongia penicillata ogilbyi), and compared them with 231 (n = 152 for mtDNA) modern samples. In modern woylie populations 15 mitochondrial control region (CR) haplotypes were identified. Interestingly, mtDNA CR data from only 29 historical samples demonstrated 15 previously unknown haplotypes and detected an extinct divergent clade. Through modelling, we estimated the loss of CR mtDNA diversity to be between 46% and 91% and estimated this to have occurred in the past 2000–4000 years in association with a dramatic population decline. In addition, we obtained near‐complete 11‐loci microsatellite profiles from 21 historical samples. In agreement with the mtDNA data, a number of ‘new’ microsatellite alleles was only detected in the historical populations despite extensive modern sampling, indicating a nuclear genetic diversity loss >20%. Calculations of genetic diversity (heterozygosity and allelic rarefaction) showed that these were significantly higher in the past and that there was a high degree of gene flow across the woylie's historical range. These findings have an immediate impact on how the extant populations are managed and we recommend the implementation of an assisted migration programme to prevent further loss of genetic diversity. Our study demonstrates the value of integrating aDNA data into current‐day conservation strategies.     

Habitat loss and possible effects on local species richness in a species-poor system: a case study of southern Baltic Sea macrofauna

The effects of habitat loss on local species richness depend on the characteristics of the endangered system (including its total species pool and the distribution of species among the habitats). The present study focuses on the species-poor southern Baltic marine benthic biota. Macrobenthic samples were collected in three habitats: (1) soft bottom covered with vegetation; (2) stony reefs; (3) unvegetated sands. Fourty one percent of 54 observed macrozoobenthic species were habitat specific, while 30% occurred in all three habitats. There were no significant differences in total species richness among the three habitats. The accumulation curves plotted for subsets of data with selected habitats excluded lay below the curve plotted for the whole dataset, but only in one case the 95% confidence intervals of the subset curve did not overlap with those plotted for the whole dataset. The exclusion of samples from selected habitats produced a species richness drop ranging from 9 to 13%. The present study showed that habitat loss in a species-poor area with a relatively large ratio of generalist species cannot produce local species richness declines similar to those predicted for diverse marine systems. However, it must be emphasized that in species-poor systems, the loss of ecological function accompanying habitat loss could be disproportionally higher than that predicted based on decreases in species richness, as some functions are performed by a single species.     

Biodiversity indicators in European ground waters: towards a predictive model of stygobiotic species richness

1. Estimates of species richness obtained from exhaustive field inventories over large spatial scales are expensive and time-consuming. For this reason, efficiency demands the use of indicators as 'surrogates' of species richness. Biodiversity indicators are defined herein as a limited suite of taxonomic groups the species richness of which is correlated with the species richness of all other taxonomic groups present in the survey area.
2. Species richness in ground water was assessed at different spatial scales using data collected from six regions in Europe. In total, 375 stygobiotic species were recorded across 1157 sites and 96 aquifers. The taxonomic groups collected from more than one site and with more than two species (Oligochaeta, Gastropoda, Cyclopoida, Harpacticoida, Ostracoda, Isopoda, Amphipoda, Bathynellacea and Acari) were used to develop nonparametric models to predict stygobiotic biodiversity at the aquifer scale.
3. Pair-wise correlations between taxonomic groups were low, i.e. variation in species richness of a single taxonomic group did not usually reflect variation of the other groups. In contrast, multiple regressions calculated between species richness of any combination of taxa and extra-group species richness along the six regions resulted in a number of significant relationships.
4. These results suggest that some taxonomic groups (mainly Copepoda and Amphipoda and, to a lesser extent, Oligochaeta and Gastropoda) combined in different ways across the regions, were good biodiversity indicators in European groundwater ecosystems. However, the uneven distribution of taxonomic groups prevented selection of a common set of indicators for all six regions. Faunal differences among regions are presumably related to both historical and ecological factors, including palaeogeography, palaeoecology, geology, aquifer fragmentation and isolation, and, less clearly, anthropogenic disturbance.     

Experimental evidence for the effects of dung beetle functional group richness and composition on ecosystem function in a tropical forest

Much of the literature on the relationship between species richness or functional group richness and measures of ecosystem function focuses on a restricted set of ecosystem function measures and taxonomic groups. Few such studies have been carried out under realistic levels of diversity in the field, particularly in high diversity ecosystems such as tropical forests. We used exclusion experiments to study the effects of dung beetle functional group richness and composition on two interlinked and functionally important ecological processes, dung removal and secondary seed dispersal, in evergreen tropical forest in Sabah, Malaysian Borneo. Overall, both dung and seed removal increased with dung beetle functional group richness. However, levels of ecosystem functioning were idiosyncratic depending on the identity of the functional groups present, indicating an important role for functional group composition. There was no evidence for interference or competition among functional groups. We found strong evidence for overyielding and transgressive overyielding, suggesting complementarity or facilitation among functional groups. Not all mixtures showed transgressive overyielding, so that complementarity was restricted to particular functional group combinations. Beetles in a single functional group (large nocturnal tunnellers) had a disproportionate influence on measures of ecosystem function: in their absence dung removal is reduced by approximately 75%. However, a full complement of functional groups is required to maximize ecosystem functioning. This study highlights the importance of both functional group identity and species composition in determining the ecosystem consequences of extinctions or altered patterns in the relative abundance of species.     

Origins of species richness in the Indo‐Malay‐Philippine biodiversity hotspot: evidence for the centre of overlap hypothesis

The Indo‐Malay‐Philippine (IMP) biodiversity hotspot, bounded by the Philippines, the Malay Peninsula and New Guinea, is the epicentre of marine biodiversity. Hypotheses to explain the source of the incredible number of species found there include the centre of overlap hypothesis, which proposes that in this region the distinct faunas of the Pacific and Indian Oceans overlap. Here we review the biogeographical evidence in support of this hypothesis. We examined tropical reef fish distributions, paying particular attention to sister species pairs that overlap in the IMP hotspot. We also review phylogeographical studies of wide‐ranging species for evidence of lineage divergence and overlap in the IMP region. Our synthesis shows that a pattern of isolation between the Pacific and the Indian Ocean faunas is evident across a wide range of taxa. The occurrence of sister species, with one member in each ocean, indicates that the mechanism(s) of isolation has been in effect since at least the Miocene, while phylogeographical studies indicate more recent divergences in the Pleistocene. Divergence in isolation followed by population expansion has led to an overlap of closely related taxa or genetic lineages in the hotspot, contributing to diversity and species richness in the region. These findings are consistent with the centre of overlap hypothesis and highlight the importance of this process in generating biodiversity within the IMP.