Home About us Contact
|
Home About us Contact | ||
|
|
||
Published Data Sets (published + data_set)
Selected AbstractsThe evolution of rewards: seed dispersal, seed size and elaiosome sizeJOURNAL OF ECOLOGY, Issue 3 2006WILL EDWARDS Summary 1We examine the relationship between the reward offered to ants to disperse seeds (elaiosome size) and seed size, and the possible mechanisms that may generate this relationship in Australian plant species. 2We used seed and elaiosome sizes from our own data set containing 87 Acacia species, supplemented with 22 species from a previously published data set, and 98 ,Other species' from 51 genera in 25 families, also from published data. 3The relationship between ln(elaiosome size) and ln(seed size) was determined using standard major axis (SMA) regression for both data sets. For the Other data set we also determined the relationship among species independent of the differences between genera, among genera independent of the differences between families, among genera and among families. We used SMA to test for differences in slopes between groups. 4We found a significant common slope amongst all subsets of the larger data set. The estimated common slope and the 95% confidence interval for the relationship between ln(elaiosome size) and ln(seed size) across all data sets fell above one (1.24, 95%CI = 1.17,1.32), suggesting positive allometry. Slopes were also significantly positive and strikingly similar between the Acacia species data set and the Other species data sets. Similar positive allometry was shown in the ,other' species data set among genera and families, and among species independent of genus means (,species effects'). 5Significant and consistent relationships between taxonomic levels, independent of relationships at other levels, along with significant relationships at the species level, and similarity of slopes, suggest independent convergence towards an underlying functional relationship that has persisted over long evolutionary periods. Our results therefore suggest that ants have been agents of selection on seed traits. 6Such a functional relationship might result from a trade-off in ant foraging behaviour between the benefit of the reward (elaiosome) and the cost of the dispersal (determined by seed size). Slopes > 1 would then suggest that ants need more than proportionally larger rewards to remove larger seeds. [source] Energetic costs, underlying resource allocation patterns, and adaptive value of predator-induced life-history shiftsOIKOS, Issue 2 2008Karsten Rinke We studied costs and benefits of life history shifts of water fleas (genus Daphnia) in response to infochemicals from planktivorous fish. We applied a dynamic energy budget model to investigate the resource allocation patterns underlying the observed life history shifts and their adaptive value under size selective predation in one coherent analysis. Using a published data set of life history shifts in response to fish infochemicals we show that Daphnia invests less energy in somatic growth in the fish treatment. This observation complies with theoretical predictions on optimal resource allocation. However, the observed patterns of phenotypic plasticity cannot be explained by changes in resource allocation patterns alone because our model-based analysis of the empirical data clearly identified additional bioenergetic costs in the fish treatments. Consequently, the response to fish kairomone only becomes adaptive if the intensity of size selective predation surpasses a certain critical level. We believe that this is the first study that puts resource allocation, energetic costs, and adaptive value of predator induced life-history shifts , using empirical data , into one theoretical framework. [source] Applying species-sensitivity distributions in ecological risk assessment: Assumptions of distribution type and sufficient numbers of species,ENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 2 2000Michael C. Newman Abstract Species-sensitivity distribution methods assemble single-species toxicity data to predict hazardous concentrations (HCps) affecting a certain percentage (p) of species in a community. The fit of the lognormal model and required number of individual species values were evaluated with 30 published data sets. The increasingly common assumption that a lognormal model best fits these data was not supported. Fifteen data sets failed a formal test of conformity to a lognormal distribution; other distributions often provided better fit to the data than the lognormal distribution. An alternate bootstrap method provided accurate estimates of HCp without the assumption of a specific distribution. Approximate sample sizes producing HC5 estimates with minimal variance ranged from 15 to 55, and had a median of 30 species-sensitivity values. These sample sizes are higher than those suggested in recent regulatory documents. A bootstrap method is recommended that predicts with 95% confidence the concentration affecting 5% or fewer species. [source] The lognormal distribution is not an appropriate null hypothesis for the species,abundance distributionJOURNAL OF ANIMAL ECOLOGY, Issue 3 2005MARK WILLIAMSON Summary 1Of the many models for species,abundance distributions (SADs), the lognormal has been the most popular and has been put forward as an appropriate null model for testing against theoretical SADs. In this paper we explore a number of reasons why the lognormal is not an appropriate null model, or indeed an appropriate model of any sort, for a SAD. 2We use three empirical examples, based on published data sets, to illustrate features of SADs in general and of the lognormal in particular: the abundance of British breeding birds, the number of trees > 1 cm diameter at breast height (d.b.h.) on a 50 ha Panamanian plot, and the abundance of certain butterflies trapped at Jatun Sacha, Ecuador. The first two are complete enumerations and show left skew under logarithmic transformation, the third is an incomplete enumeration and shows right skew. 3Fitting SADs by ,2 test is less efficient and less informative than fitting probability plots. The left skewness of complete enumerations seems to arise from a lack of extremely abundant species rather than from a surplus of rare ones. One consequence is that the logit-normal, which stretches the right-hand end of the distribution, consistently gives a slightly better fit. 4The central limit theorem predicts lognormality of abundances within species but not between them, and so is not a basis for the lognormal SAD. Niche breakage and population dynamical models can predict a lognormal SAD but equally can predict many other SADs. 5The lognormal sits uncomfortably between distributions with infinite variance and the log-binomial. The latter removes the absurdity of the invisible highly abundant half of the individuals abundance curve predicted by the lognormal SAD. The veil line is a misunderstanding of the sampling properties of the SAD and fitting the Poisson lognormal is not satisfactory. A satisfactory SAD should have a thinner right-hand tail than the lognormal, as is observed empirically. 6The SAD for logarithmic abundance cannot be Gaussian. [source] Measuring the components of competition along productivity gradientsJOURNAL OF ECOLOGY, Issue 2 2007MARK V. WILSON Summary 1Controversy surrounds the measurement of competition intensity. Moreover, when biomass varies systematically along productivity and other environmental gradients, common indices of competitive outcome mask important ecological interactions. 2This study presents two indices derived from how neighbours interact with target plants. The first, relative crowding, increases directly with the abundance of neighbours present and decreases inversely with the potential size and vigour of the target plant itself. The second, interaction strength, is the integral of suppression of the target by neighbours over the range of neighbour abundance. Relative crowding and interaction strength are derived independently, but when multiplied produce the commonly used relative competitive index, showing the biological underpinnings of the relative competition index in terms of crowding and strength of interaction. Since the new indices of relative crowding and interaction strength explicitly account for the amount of neighbour biomass, they serve as a valid method to track the effects of changing habitat conditions on the components of competition. 3The new indices are applied to three published data sets. In each case, relative crowding increased with standing crop. In one case competition was reported as unchanged along a productivity gradient, whereas the new indices show that relative crowding and interaction strength both had significant patterns, but their effects were counteracting. These results do not fit current theories of competition. Further empirical studies are needed to see if competition theory needs revision. 4Separating the mechanisms of competition into relative crowding and strength of interaction reveals previously hidden patterns that help bring to light underlying processes of competition along productivity gradients. [source] Modelling advection and diffusion of water isotopologues in leavesPLANT CELL & ENVIRONMENT, Issue 8 2007MATTHIAS CUNTZ ABSTRACT We described advection and diffusion of water isotopologues in leaves in the non-steady state, applied specifically to amphistomatous leaves. This explains the isotopic enrichment of leaf water from the xylem to the mesophyll, and we showed how it relates to earlier models of leaf water enrichment in non-steady state. The effective length or tortuosity factor of isotopologue movement in leaves is unknown and, therefore, is a fitted parameter in the model. We compared the advection,diffusion model to previously published data sets for Lupinus angustifolius and Eucalyptus globulus. Night-time stomatal conductance was not measured in either data set and is therefore another fitted parameter. The model compared very well with the observations of bulk mesophyll water during the whole diel cycle. It compared well with the enrichment at the evaporative sites during the day but showed some deviations at night for E. globulus. It became clear from our analysis that night-time stomatal conductance should be measured in the future and that the temperature dependence of the tracer diffusivities should be accounted for. However, varying mesophyll water volume did not seem critical for obtaining a good prediction of leaf water enrichment, at least in our data sets. In addition, observations of single diurnal cycles do not seem to constrain the effective length that relates to the tortuosity of the water path in the mesophyll. Finally, we showed when simpler models of leaf water enrichment were suitable for applications of leaf water isotopes once weighted with the appropriate gas exchange flux. We showed that taking an unsuitable leaf water enrichment model could lead to large biases when cumulated over only 1 day. [source] Genetic structure of Eurasian cattle (Bos taurus) based on microsatellites: clarification for their breed classification,ANIMAL GENETICS, Issue 2 2010M.-H. Li Summary We pool three previously published data sets and present population genetic analyses of microsatellite variation in 48 Bos taurus cattle breeds from a wide range of geographical origins in Eurasia, mostly its northern territory. Bayesian model-based clustering reveals six distinct clusters: besides a single-population cluster of the Yakutian Cattle from Far Eastern Siberia and a cluster of breeds characteristic of an early origin, the other four major clusters largely correspond to previously defined morphological subgroups of Red Lowland, Lowland Black-Pied, Longhorned Dairy and North European Polled cattle breeds. The results highlighted past expansion events of the productive breeds such as Danish Red, Angeln, Holstein-Friesian and Ayrshire in northern and Eastern Europe. Based on genetic assignment of the breeds and the availability of breed information, we provide a preliminary classification of the five breeds that were to date undefined. Furthermore, in the analysis of molecular variance, despite some correspondence between geographical proximity and genetic similarity, the breed classification appears to be a better predictor of genetic structure in the cattle populations (the among-group variance component: breed classification, 2.47%, P < 0.001; geographical division, 0.77%, P < 0.001). [source] | ||||||||||