Local Dispersal (local + dispersal)

Distribution by Scientific Domains


Selected Abstracts


Sex ratio and maturity indicate the local dispersal and mortality of adult stoneflies

FRESHWATER BIOLOGY, Issue 8 2006
I. PETERSEN
Summary 1.,Despite a recent upsurge in interest, there remains remarkably little information about the dispersal and survival of the adults of most stream-dwelling insects, although this is a basic requirement for understanding their long-term population dynamics. 2.,Using Malaise traps for a whole annual flight period, we captured adult stoneflies (Leuctra nigra) along transects perpendicular to three upland Welsh streams. We assessed spatial and temporal patterns in sex ratio to infer local dispersal and, using maturity as an age marker, estimated the mortality of adult females. 3.,Nearly all adult stoneflies (99%) were taken in the period 26 April,23 July, and the onset of the male and female flight periods was the same. Most males (90%) had been caught by late June. Females were classified as immature (without ripe eggs) or mature, and 90% of immature females had been caught by mid-late June (depending on catchment). As immature females declined in the catch, mature females increased, 10% having been caught by late-May to early June and 90% by early to mid-July. The median catches of immature and mature females were separated by 32 days in all three catchments. 4.,There was a female bias in the sex ratio overall, which increased as time passed and was attributable partially to the greater longevity of females. Late in the flight period, however, female bias was also greater near the stream channel implying a return of mature females (but not males) from the riparian vegetation, presumably to oviposit. 5.,The number of mature females was less than the number of immatures in two of the three channels. Over all three catchments, the overall mortality of females over the 32 days taken to mature was estimated at 29%, equivalent to an exponential daily rate of 1.1% day,1. The apparently negative mortality rate in one catchment (i.e. more matures than immatures being caught) could be due to an influx of adult females from elsewhere along the channel to oviposit. 6.,Natural markers of age and population structure, such as sex ratio and female maturity, thus enabled us to detect a return of females to the stream to oviposit, after prior limited dispersal into the riparian zone, and to infer longitudinal movements in search of suitable sites. We were also able to estimate mortality in the field. Such natural markers seem to have been underexploited in the study of adult aquatic insects. [source]


Plant colonization after managed realignment: the relative importance of diaspore dispersal

JOURNAL OF APPLIED ECOLOGY, Issue 4 2005
MINEKE WOLTERS
Summary 1Deliberate breaching of sea defences is frequently practised with the aim of restoring salt-marsh vegetation on previously embanked land. However, experience so far has shown that it may take several years before salt-marsh vegetation is fully established, and it is possible that limited diaspore dispersal plays a role in this. In order to ascertain whether salt-marsh development may be constrained by limited diaspore dispersal, we studied the dispersal of salt-marsh species by tidal water. 2From October 2001 to the end of March 2002 a total of 38 species, of which 18 were salt-marsh species, was trapped in a restoration site and adjacent marsh. Aster tripolium, Limonium vulgare, Puccinellia maritima, Salicornia spp., Spergularia media and Suaeda maritima were the most abundant salt-marsh species, with more than 3 diaspores m,2 trapped during the study period. 3For most species, the number of diaspores trapped was representative of their abundance in nearby vegetation. Hence, despite the potential for long-distance transport by tidal water, our results indicate a predominantly local dispersal of salt-marsh species. 4Synthesis and applications. For the restoration of salt-marsh vegetation after de-embankment, relatively rapid colonization may be expected from pioneer and low-marsh species, provided they are present in a nearby source area and the restoration site is at the appropriate altitude. The establishment of species absent from the adjacent marsh may be dependent on the presence of birds or humans as the main dispersal agents. Breaching of sea defences should preferably take place before or during September, in order to take advantage of the peak in dispersal of salt-marsh species in the first year after breaching. [source]


Offspring-driven local dispersal in female sand lizards (Lacerta agilis)

JOURNAL OF EVOLUTIONARY BIOLOGY, Issue 6 2004
K. Ryberg
Abstract We report on a field study in which determinants of female breeding dispersal (i.e. the shift in the mean home range coordinates between successive breeding events) was investigated. Offspring were released in full sib groups (or half sib ones if there was within-clutch multiple paternity) at a separation distance from the females that varied between ,families'. This allowed for analysis of ,offspring nearness' effects on maternal dispersal. When a female's offspring were released more closely to her, she responded with greater dispersal. Furthermore, when the data set was truncated at 100 m maternal,offspring separation distance at offspring release (because perception at longer distances is likely to be unrealistic), maternal dispersal resulted in greater separation distance between female and offspring in the following year. A corresponding analysis for juveniles revealed no effect of maternal nearness on offspring dispersal but identified a significant effect of clutch size, to our surprise with dispersal declining with increasing clutch size. We discuss this result in a context of the ,public information hypothesis' (reinterpreted for juveniles in a nonsocial foraging species), suggesting that conspecific abundance perhaps acts as an indicator of local habitat quality. Thus, our analysis suggests a microgeographic structuring of the adult female population driven by genetic factors, either through inbreeding avoidance, or from simply avoiding individuals with a similar genotype regardless of their pedigree relatedness, while a nongenetic factor seems more important in their offspring. [source]


Which traits promote persistence of feral GM crops?

OIKOS, Issue 1 2005
Part 2: implications of metapopulation structure
Transgenes may spread from crops into the environment via the establishment of feral populations, often initiated by seed spill from transport lorries or farm machinery. Locally, such populations are often subject to large environmental variability and usually do not persist longer than a few years. Because secondary feral populations may arise from seed dispersal to adjacent sites, the dynamics of such populations should be studied in a metapopulation context. We study a structured metapopulation model with local dispersal, mimicking a string of roadside subpopulations of a feral crop. Population growth is assumed to be subject to local disturbances, introducing spatially random environmental stochasticity. Our aim is to understand the role of dispersal and environmental variability in the dynamics of such ephemeral populations. We determine the effect of dispersal on the extinction boundary and on the distribution of persistence times, and investigate the influence of spatially correlated disturbances as opposed to spatially random disturbances. We find that, given spatially random disturbances, dispersal slows down the decline of the metapopulation and results in the occurrence of long-lasting local populations which remain more or less static in space. We identify which life history traits, if changed by genetic modification, have the largest impact on the population growth rate and persistence times. For oilseed rape, these are seed bank survival and dormancy. Combining our findings with literature data on transgene-induced life history changes, we predict that persistence is promoted by transgenes for oil-modifications (high stearate or high laurate) and, possibly, for insect resistence (Bt). Transgenic tolerance to glufosinate herbicide is predicted to reduce persistence. [source]


Dispersal kernels of the invasive alien western corn rootworm and the effectiveness of buffer zones in eradication programmes in Europe

ANNALS OF APPLIED BIOLOGY, Issue 1 2010
L.R. Carrasco
Europe is attempting to contain or, in some regions, to eradicate the invading and maize destroying western corn rootworm (WCR). Eradication and containment measures include crop rotation and insecticide treatments within different types of buffer zones surrounding new introduction points. However, quantitative estimates of the relationship between the probability of adult dispersal and distance from an introduction point have not been used to determine the width of buffer zones. We address this by fitting dispersal models of the negative exponential and negative power law families in logarithmic and non-logarithmic form to recapture data from nine mark-release-recapture experiments of marked WCR adults from habitats as typically found in the vicinity of airports in southern Hungary in 2003 and 2004. After each release of 4000,6300 marked WCR, recaptures were recorded three times using non-baited yellow sticky traps at 30,305 m from the release point and sex pheromone-baited transparent sticky traps placed at 500,3500 m. Both the negative exponential and negative power law models in non-log form presented the best overall fit to the numbers of recaptured adults (1% recapture rate). The negative exponential model in log form presented the best fit to the data in the tail. The models suggested that half of the dispersing WCR adults travelling along a given bearing will have travelled between 117 and 425 m and 1% of the adults between 775 and 8250 m after 1 day. An individual-based model of dispersal and mortality over a generation of WCR adults indicated that 9.7,45.3% of the adults would escape a focus zone (where maize is only grown once in 3 consecutive years) of 1 km radius and 0.6,21% a safety zone (where maize is only grown once in 2 consecutive years) of 5 km radius and consequently current European Commission (EC) measures are inadequate for the eradication of WCR in Europe. Although buffer zones large enough to allow eradication would be economically unpalatable, an increase of the minimum width of the focus zone from 1 to 5 km and the safety zone from 5 to 50 km would improve the management of local dispersal. [source]