Historical stability of diversity patterns in African estrildid finches (Aves: Estrildidae)?

Studying shifts in species diversity through time and space is an essential component of many aspects of biogeography and ecology. In this study, we predict the potential distribution of 61 species of African estrildid finches in order to assess current and past diversity patterns. Models were projected onto two climatic scenarios (Community Climate System Model, CCSM, and Model for Interdisciplinary Research on Climate, MIROC) representing past climate conditions, as might be expected during the Last Glacial Maximum 21 000 years BP. Subsequent overlays of the resulting potential distributions were conducted under different dispersal assumptions and compared with expert maps. Our results suggest highly similar current distribution patterns obtained by both methods. Projections onto Pleistocene scenarios showed similar patterns, with only small differences under limited and unlimited dispersal assumptions. Looking separately at diversity patterns predicted for forest and savannah species, diversity hot spots of forest species under MIROC conditions were consistent with suggested forest refugia, but were inconsistent under CCSM conditions. According to our models, savannah species were more widely distributed during the cooler and drier conditions of the Pleistocene. By using ecological niche models we show that current diversity patterns of a whole species group may have changed only slightly since the Pleistocene, suggesting a pattern of general spatial stability. However, we emphasize the importance of using different climatic scenarios as well as including the supposed dispersal of organisms in the modelling, as these factors influence results on a broad scale. © 2011 The Linnean Society of London, Biological Journal of the Linnean Society, 2011, 102 , 455–470.     

STUDIES ON THE UPTAKE AND TRANSLOCATION OF STREPTOMYCIN BY PEACH SEEDLINGS

Measurements of the antibiotic activity in the foliage of peach seedlings, kept with their roots in mineral nutrient solutions containing streptomycin, showed that streptomycin passed into the foliage and sometimes reached concentrations above those of the solutions surrounding the roots. The amount of the antibiotic in leaves varied with the time that roots were kept in the solutions and with the streptomycin concentrations of the solutions. Lower leaves contained much more than upper leaves.
Adding macerated leaf tissue to streptomycin solutions decreased the amount of streptomycin detectable in the supernatant liquid more than could be accounted for by dilution or alteration of pH.
Streptomycin first affected plants by decreasing apical growth, but at higher concentrations it caused chlorotic and necrotic areas on leaves and stems.     

Floodplain ants show a stronger response to an extensive flood than to variations in fallen‐timber load

Understanding how species respond to differences in resource availability is critical to managing biodiversity under the increasing pressures associated with climate change and growing human populations. Over the last century, the floodplain forests of Australia's largest river system, the Murray‐Darling Basin, have been much affected by intensive harvesting of timber and firewood, and increasingly stressed by river regulation and, recently, an extended drought. Fallen timber – logs and shed branches – is known to play a key role in the ecology of several important species on these floodplains. Here, we monitored the response of the ant assemblages of a floodplain forest along the Murray River to a large‐scale (34 ha) experimental manipulation of fallen‐timber load (0 to 80 t ha^?1) over 4 years. The forest was subjected to an incidental, extensive flood that enabled us to examine how two important stressors (timber removal and river regulation) affect ant assemblages. Ants showed little response to the proximity of fallen timber within plots, prior to the flood, or to different loads among plots, unlike other floodplain biota. After the flood, both ant abundance and species richness increased and species composition changed. However, this increase in species richness after flooding was less pronounced in plots with higher amounts of fallen timber. Managing river red gum forest using a mosaic of flood regimes, more representative of historical conditions, is likely to be the most effective way to maintain and enhance the diversity of ants and other biota on these important floodplains.     

Habitat use by the inland carpet python (Morelia spilota metcalfei: Pythonidae): Seasonal relationships with habitat structure and prey distribution in a rural landscape

Abstract Squamate reptiles are significant components of woodland vertebrate communities in eastern Australia, but their ecology is poorly understood. We investigated seasonal variation in habitat use by the Inland Carpet Python, Morelia spilota metcalfei Wells and Wellington (Pythonidae), a threatened snake that inhabits the woodland environments of the Murray–Darling Basin. Nine pythons were radiotracked within and near the Mount Meg Flora and Fauna Reserve in north‐eastern Victoria to investigate how habitat structure and prey distribution (namely, that of the European Rabbit, Oryctolagus cuniculus L. (Leporidae)) influenced seasonal movement patterns. Data were analysed over three spatial scales to allow firm interpretations regarding resource selection. Pythons exhibited distinct seasonal trends in habitat use. During the cooler spring months, snakes chose warm, well‐insulated microhabitats, primarily rocky outcrops on north‐ and north‐west‐facing hillsides. Pythons moved widely during the summer months, apparently in search of prey. Snake localities could be readily linked to rabbit distribution at this time. Specifically, snakes moved to more open, disturbed habitats that contained a high density of rabbits, and consistently selected microhabitats in close proximity to rabbit burrows. In autumn, habitat use was transitional, as snakes progressively returned to the rocky hillsides where they overwintered. Thus, trends in habitat use were influenced by the snakes' thermoregulatory and foraging strategies. Careful management of specific habitats and feral prey populations is required to conserve populations of this endangered snake.     

Assessing the eddy covariance technique for evaluating carbon dioxide exchange rates of ecosystems: past, present and future

The eddy covariance technique ascertains the exchange rate of CO₂ across the interface between the atmosphere and a plant canopy by measuring the covariance between fluctuations in vertical wind velocity and CO₂ mixing ratio. Two decades ago, the method was employed to study CO₂ exchange of agricultural crops under ideal conditions during short field campaigns. During the past decade the eddy covariance method has emerged as an important tool for evaluating fluxes of carbon dioxide between terrestrial ecosystems and the atmosphere over the course of a year, and more. At present, the method is being applied in a nearly continuous mode to study carbon dioxide and water vapor exchange at over a hundred and eighty field sites, worldwide. The objective of this review is to assess the eddy covariance method as it is being applied by the global change community on increasingly longer time scales and over less than ideal surfaces. The eddy covariance method is most accurate when the atmospheric conditions (wind, temperature, humidity, CO₂) are steady, the underlying vegetation is homogeneous and it is situated on flat terrain for an extended distance upwind. When the eddy covariance method is applied over natural and complex landscapes or during atmospheric conditions that vary with time, the quantification of CO₂ exchange between the biosphere and atmosphere must include measurements of atmospheric storage, flux divergence and advection. Averaging CO₂ flux measurements over long periods (days to year) reduces random sampling error to relatively small values. Unfortunately, data gaps are inevitable when constructing long data records. Data gaps are generally filled with values produced from statistical and empirical models to produce daily and annual sums of CO₂ exchange. Filling data gaps with empirical estimates do not introduce significant bias errors because the empirical algorithms are derived from large statistical populations. On the other hand, flux measurement errors can be biased at night when winds are light and intermittent. Nighttime bias errors tend to produce an underestimate in the measurement of ecosystem respiration. Despite the sources of errors associated with long‐term eddy flux measurements, many investigators are producing defensible estimates of annual carbon exchange. When measurements come from nearly ideal sites the error bound on the net annual exchange of CO₂ is less than ±50 g C m^?2 yr^?1. Additional confidence in long‐term measurements is growing because investigators are producing values of net ecosystem productivity that are converging with independent values produced by measuring changes in biomass and soil carbon, as long as the biomass inventory studies are conducted over multiple years.     

Latitudinal patterns of magnitude and interannual variability in net ecosystem exchange regulated by biological and environmental variables

Over the last two and half decades, strong evidence showed that the terrestrial ecosystems are acting as a net sink for atmospheric carbon. However the spatial and temporal patterns of variation in the sink are not well known. In this study, we examined latitudinal patterns of interannual variability (IAV) in net ecosystem exchange (NEE) of CO₂ based on 163 site-years of eddy covariance data, from 39 northern-hemisphere research sites located at latitudes ranging from ∼29°N to ∼64°N. We computed the standard deviation of annual NEE integrals at individual sites to represent absolute interannual variability (AIAV), and the corresponding coefficient of variation as a measure of relative interannual variability (RIAV). Our results showed decreased trends of annual NEE with increasing latitude for both deciduous broadleaf forests and evergreen needleleaf forests. Gross primary production (GPP) explained a significant proportion of the spatial variation of NEE across evergreen needleleaf forests, whereas, across deciduous broadleaf forests, it is ecosystem respiration (Re). In addition, AIAV in GPP and Re increased significantly with latitude in deciduous broadleaf forests, but AIAV in GPP decreased significantly with latitude in evergreen needleleaf forests. Furthermore, RIAV in NEE, GPP, and Re appeared to increase significantly with latitude in deciduous broadleaf forests, but not in evergreen needleleaf forests. Correlation analyses showed air temperature was the primary environmental factor that determined RIAV of NEE in deciduous broadleaf forest across the North American sites, and none of the chosen climatic factors could explain RIAV of NEE in evergreen needleleaf forests. Mean annual NEE significantly increased with latitude in grasslands. Precipitation was dominant environmental factor for the spatial variation of magnitude and IAV in GPP and Re in grasslands.     

The Role of Tree Gaps in Maintaining the Population Structure of a Woodland Herb: Cynoglossum virginianum L.

Abstract Tree gaps may be important habitats for the establishment and spread of understory herbs in eastern (US) deciduous forests. Data from past studies, however, have not shown any clear patterns for either species diversity or increased percent cover. The lack of clear patterns of response to gaps by herbs may be due to evolutionary differences among species or, in part, due to the fact that most studies have been short-term and long-term patterns have, therefore, not been observed. In addition, few studies have considered the responses of individual genets and/or ramets. We have been conducting a long-term study of Cynoglossum virginianum , now in its 16th year, to determine subpopulation and individuals' responses in gap and non-gap habitats. A larger percentage of individuals flowered in the gap subpopulation shortly after it was created. Seed production rates were also higher in the gap subpopulation. The long-term benefits gained by the short-term flowering response have, however, been few as all but two of the seedlings produced within a few years of gap formation have died. In addition, all of individuals that flowered and produced seeds decreased in size and most have remained in the smaller size classes. In addition, only one of the individuals in the gap subpopulation has flowered since the initial flowering response while plants in non-gap subpopulations have flowered and produced seeds throughout the study period. Gaps may only be beneficial to C. virginianum if seeds are dispersed into non-gap areas or if seeds can remain dormant in the soil until conditions are more suitable for seedling survival.     

The moult of Barred Warblers Sylvia nisoria in Kenya—evidence for a split wing-moult pattern initiated during the birds' first winter*

The moult of Barred Warblers Sylvia nisoria was studied during three winter seasons in southeastern Kenya at a southward passage site (Ngulia) and a wintering site (Mtito Andei). Most Barred Warblers migrating through Ngulia in November had yet to commence winter moult. These birds probably moulted subsequently in winter in northern Tanzania. In December, birds were found in heavy moult at Mtito Andei, and some of these birds were known to stay throughout the winter. By contrast, most birds reaching southeastern Kenya from late December onwards had already completed part or all of their winter moult, presumably at stopover sites in northern and eastern Kenya or in Ethiopia. Thus, winter moult in Barred Warblers takes place mainly in late November and December, either just before or soon after the final leg of autumn migration. In general, first-year birds renewed all tertials and tail feathers, about three to five secondaries per wing and commonly also the outer one to four large primaries per wing. Adults renewed all tertials and tail feathers, almost all secondaries and only occasionally an outer primary. The replacement of relatively fresh juvenile secondaries during the birds' first winter implies that the split moult pattern of this species (secondaries, tertials and tail moulted in winter; primaries and tertials in summer) is endogenously controlled.     

Migration, stopover and moult of the Great Reed Warbler Acrocephalus arundinaceus in Ghana, West Africa

We studied Great Reed Warblers Acrocephalus arundinaceus at two localities in Ghana during the winter. In the north (Tono), the birds arrived from late September and conducted a rapid moult soon after arrival. Towards the end of moult, birds accumulated fat and disappeared from the site. In the south (Tafo), birds arrived from mid-November in fresh plumage. This seemed to be the final wintering area as birds stayed there during the winter. In March-April they again accumulated fat, although only small amounts, before spring migration back to breeding areas.