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Marine megafauna species are affected by a wide range of anthropogenic threats. To evaluate the risk of such threats, species’ vulnerability to each threat must first be determined. We build on the existing threats classification scheme and ranking system of the International Union for Conservation of Nature (IUCN) Red List of Threatened Species by assessing the vulnerability of 256 marine megafauna species to 23 at‐sea threat...
A Transcriptomic Comparative Study of Cranial VasculatureNARA Subscribed
Fox control and fire influence the occurrence of invasive predators and threatened native preyNARA Subscribed
It can be challenging to distinguish management impacts from other population drivers, including ‘natural’ processes and co-occurring threats. However, disentangling processes is important, particularly when management may have unintended consequences, such as mesopredator release. We explored the effects of long-term, broadscale poison-baiting programs on the distribution of red foxes Vulpes vulpes (targeted invasive predator...
Marine nutrient subsidies promote biogeochemical hotspots in undisturbed, highly humic estuariesNARA Subscribed
The land‐ocean dissolved organic carbon (DOC) flux represents a significant term within the global carbon budget, with peatland‐dominated regions representing the most intense sources of terrestrial DOC export. As the interface between freshwater and marine systems, estuaries have the potential to act as a filter of the land‐ocean carbon flux, removing terrestrially derived DOC, which is present at low concentrations in the oc...
Effects of human footprint and biophysical factors on the body‐size structure of fished marine speciesNARA Subscribed
Marine fisheries in coastal ecosystems in many areas of the world have historically removed large‐bodied individuals, potentially impairing ecosystem functioning and the long‐term sustainability of fish populations. Reporting on size‐based indicators that link to food‐web structure can contribute to ecosystem‐based management, but the application of these indicators over large (cross‐ecosystem) geographical scales has been lim...
Marine reserves are a key tool for the conservation of marine biodiversity, yet only ~2.5% of the world's oceans are protected. The integration of marine reserves into connected networks representing all habitats has been encouraged by international agreements, yet the benefits of this design has not been tested empirically. Australia has one of the largest systems of marine reserves, providing a rare opportunity to assess how...
Large birds travel farther in homogeneous environmentsNARA Subscribed
Aim Animal movement is an important determinant of individual survival, population dynamics and ecosystem structure and function. Nonetheless, it is still unclear how local movements are related to resource availability and the spatial arrangement of resources. Using resident bird species and migratory bird species outside the migratory period, we examined how the distribution of resources affects the movement patterns of both...
Strong responses from weakly interacting speciesNARA Subscribed
The impact of species loss from competitive communities partly depends on how populations of the surviving species respond. Predicting the response should be straightforward using models that describe population growth as a function of competitor densities; but these models require accurate estimates of interaction strengths. Here, we quantified how well we could predict responses to competitor removal in a community of annual...
Latitudinal gradients in biotic interactions have been suggested as causes of global patterns of biodiversity and phenotypic variation. Plant biologists have long speculated that outcrossing mating systems are more common at low than high latitudes owing to a greater predictability of plant–pollinator interactions in the tropics; however, these ideas have not previously been tested. Here, we present the first global biogeograp...
The effects of asymmetric interactions on population dynamics has been widely investigated, but there has been little work aimed at understanding how life history parameters like generation time, life expectancy and the variance in lifetime reproductive success are impacted by different types of competition. We develop a new framework for incorporating trait‐mediated density‐dependence into size‐structured models and use Trini...
Competition on productivity gradients – what do we expect?NARA Subscribed
Many experimental studies have quantified how the effects of competition vary with habitat productivity, with the results often interpreted in terms of the ideas of Grime and Tilman. Unfortunately, these ideas are not relevant to many experiments, and so we develop an appropriate resource competition model and use this to explore the effects of habitat productivity on the intensity of competition. Several mechanisms influencin...
Plant growth rates and seed size: a re‐evaluationNARA Subscribed
Small‐seeded plant species are often reported to have high relative growth rate or RGR. However, because RGR declines as plants grow larger, small‐seeded species could achieve higher RGR simply by virtue of their small size. In contrast, size‐standardized growth rate or SGR factors out these size effects. Differences in SGR can thus only be due to differences in morphology, allocation, or physiology. We used nonlinear regressi...