199 research outputs found
Generalized drivers in the mammalian endangerment process
An important challenge for conservation today is to understand the endangerment process and identify any generalized patterns in how threats occur and aggregate across taxa. Here we use a global database describing main current external threats in mammals to evaluate the prevalence of distinct threatening processes, primarily of anthropogenic origin, and to identify generalized drivers of extinction and their association with vulnerability status and intrinsic species' traits. We detect several primary threat combinations that are generally associated with distinct species. In particular, large and widely distributed mammals are affected by combinations of direct exploitation and threats associated with increasing landscape modification that go from logging to intense human land-use. Meanwhile, small, narrowly distributed species are affected by intensifying levels of landscape modification but are not directly exploited. In general more vulnerable species are affected by a greater number of threats, suggesting increased extinction risk is associated with the accumulation of external threats. Overall, our findings show that endangerment in mammals is strongly associated with increasing habitat loss and degradation caused by human land-use intensification. For large and widely distributed mammals there is the additional risk of being hunted
Cars as a tool for monitoring and protecting biodiversity
Modern cars have an array of sensors that allow different objects to be recognized, including large and small animals. They thus have the potential to become a tool for monitoring biodiversity and improving driver safety. But to achieve this various challenges in computing, communications and privacy need to be addressed.info:eu-repo/semantics/publishedVersio
Which intrinsic traits predict vulnerability to extinction depends on the actual threatening processes
Understanding what makes some species more vulnerable to extinction than others is an important challenge for conservation. Many comparative analyses have addressed this issue exploring how intrinsic and extrinsic traits associate with general estimates of vulnerability. However, these general estimates do not consider the actual threats that drive species to extinction and hence, are more difficult to translate into effective management. We provide an updated description of the types and spatial distribution of threats that affect mammals globally using data from the IUCN for 5941 species of mammals. Using these data we explore the links between intrinsic species traits and specific threats in order to identify key intrinsic features associated with particular drivers of extinction. We find that families formed by small-size habitat specialists are more likely to be threatened by habitat-modifying processes; whereas, families formed by larger mammals with small litter sizes are more likely to be threatened by processes that directly affect survival. These results highlight the importance of considering the actual threatening process in comparative studies. We also discuss the need to standardize and rank threat importance in global assessments such as the IUCN Red List to improve our ability to understand what makes some species more vulnerable to extinction than others
Socioeconomic correlates of global mammalian conservation status
The main causes of biodiversity decline are related to human use of resources, which is ultimately triggered by the socioeconomic decisions made by individuals and nations. Characterizing the socioeconomic attributes of areas in which biodiversity is most threatened can help us identify decisions and conditions that promote the presence or absence of threats and potentially suggest more sustainable strategies. In this study we explored how diverse indicators of social and economic development correlate with the conservation status of terrestrial mammals within countries explicitly exploring hypothesized linear and quadratic relationships. First, comparing countries with and without threatened mammals we found that those without threatened species are a disparate group formed by European countries and Small Island Developing States (SIDS) with little in common besides their slow population growth and a past of human impacts. Second, focusing on countries with threatened mammals we found that those with a more threatened mammalian biota have mainly rural populations, are predominantly exporters of goods and services, receive low to intermediate economic benefits from international tourism, and have medium to high human life expectancy. Overall, these results provide a comprehensive characterization of the socioeconomic profiles linked to mammalian conservation status of the world's nations, highlighting the importance of transborder impacts reflected by the international flux of goods, services and people. Further studies would be necessary to unravel the actual mechanisms and threats that link these socioeconomic profiles and indicators with mammalian conservation. Nevertheless, this study presents a broad and complete characterization that offers testable hypotheses regarding how socioeconomic development associates with biodiversity
Jordan curve theorem : different approaches
RESUMEN: Se conocen muchas demostraciones del teorema de la curva de Jordan. A lo largo de éste trabajo desarrollamos en detalle algunas de estas pruebas. En primer lugar introduciremos el problema original y la conjetura, que resultó ser teorema, hecha por el propio Camille Jordan a finales del siglo XIX. Para después exponer tres demostraciones. La primera, publicada por H. Tverberg en 1980, cuyos argumentos son del tipo geométrico. En segundo lugar exponemos la prueba elaborada por R. Maehara en 1984, basada en el teorema del punto fijo de Brower. Por último veremos una demostración mediante resultados de la topologÃa algebraica, la cual podemos encontrar en el libro TopologÃa (Prentice Hall, 2000) de J.R. Munkres.ABSTRACT: There are many proofs of Jordan curve theorem. In this paper we detail some of these proofs. First we introduce the original problem and the conjeture made by Camille Jordan. Then we explain three proofs. The first, whose arguments are geometric, was published by H. Tverberg in 1980. The second was elaborated by R. Maehara in 1984 and it is a proof based on Brouwer's fixed-point theorem. Finally, we show a proof based on algebraic topology, which apppears in the book `Topology' (Prentice Hall, 2000) written by J.R. Munkres.Grado en Matemática
Road encroachment mediates species occupancy, trait filtering and dissimilarity of passerine communities
Assessing the road effects on biodiversity is challenging because impacts may depend on both wildlife responses to roads and on the spatial arrangement of roads. We questioned whether an increase in road encroachment leads to significant changes in species occurrence and community composition. Using a large citizen-science dataset of point-counts performed throughout Iberian Peninsula, we modelled the effect of road density on the occurrence of common birds (n = 78 species), while accounting for potential confounding effects of environment and survey effort. We then tested if species' occurrence patterns would be linked to specific traits related to the ability to cope with human presence. Finally, we assessed how road density affects the community compositional dissimilarity. We estimated 36 (46%) and 18 (23%) species to be negatively and positively affected by roads, respectively. Increased road encroachment was positively related with urban dwelling and fecundity, and negatively related with nesting on the ground. Furthermore, increasing road density translated into an increasing community compositional dissimilarity, mostly due to species turnover. Overall, we found that different species-specific responses to roads translate into changes at the community level. Landscape and road-network management should be conceived acknowledging that roads are contributing to biodiversity changes. As so, building upon the concepts of land sharing/land sparing, conservation actions should be tailored according to the different species responses e.g., road verge management targeting species having a positive relation with road density; and compensation actions targeting species showing a negative response toward roads.info:eu-repo/semantics/publishedVersio
Are road-kills representative of wildlife community obtained from atlas data?
Systematic road-kill surveys are useful to study the impact of roads on wildlife. However, they
are time-and budget-consuming, so the use of non-systematic data in road ecology is currently
gaining popularity (for instance, by environmental consultants). Some data sources such as atlases
(i.e., compilations of species records from a given region), which can include non-systematic and
citizen-science data, can entail several intrinsic biases, mostly due to uneven sampling effort and
uneven species detectability. Here, we tested this prediction by verifying if data from the Spanish
Atlas of Terrestrial Mammals mirror the road-kill patterns obtained from our own systematic roadkill
surveys. We focused on the Mediterranean mesocarnivore guild due to its easy identification by
citizens involved in atlas-data collection. We tested if the relative abundance of each species, their
richness and diversity obtained from Atlas and our systematic surveys were related, using linear
models, while controlling for human population and road density (potentially confounding effects).
We further compared the patterns of species abundance obtained from both sources. Our results
highlight that road-kill patterns do not mirror the Atlas patterns for the three metrics evaluated.
This is probably due to survey biases in typical data from wildlife atlases. When analysing species
individually, we found that some species are road-killed more (or less) than expected in relation
to their abundance in atlas records. These results are probably due to species-specific ecological
or behavioural traits such as species morphology or species behaviour when facing the road. We
suggest that abundance from atlas data should not be used as a proxy for road-kill rates.info:eu-repo/semantics/publishedVersio
Human-Related Factors Regulate the Spatial Ecology of Domestic Cats in Sensitive Areas for Conservation
Background: Domestic cats ranging freely in natural areas are a conservation concern due to competition, predation, disease transmission or hybridization with wildcats. In order to improve our ability to design effective control policies, we investigate the factors affecting their numbers and space use in natural areas of continental Europe.
Methodology/Principal Findings: We describe the patterns of cat presence, abundance and space use and analyse the associated environmental and human constraints in a well-preserved Mediterranean natural area with small scattered local farms. We failed in detecting cats in areas away from human settlements (trapping effort above 4000 trap-nights), while we captured 30 individuals near inhabited farms. We identified 130 cats, all of them in farms still in use by people (30% of 128 farms). All cats were free-ranging and very wary of people. The main factor explaining the presence of cats was the presence of people, while the number of cats per farm was mostly affected by the occasional food provisioning with human refuse and the presence of people. The home ranges of eight radio tagged cats were centred at inhabited farms. Males went furthest away from the farms during the mating season (3.8 km on average, maximum 6.3 km), using inhabited farms as stepping-stones in their mating displacements (2.2 km of maximum inter-farm distance moved). In their daily movements, cats notably avoided entering in areas with high fox density.
Conclusions: The presence, abundance and space use of cats were heavily dependent on human settlements. Any strategy aiming at reducing their impact in areas of conservation concern should aim at the presence of settlements and their spatial spread and avoid any access to human refuse. The movements of domestic cats would be limited in areas with large patches of natural vegetation providing good conditions for other carnivore mammals such as red foxes.Peer reviewe
Management-Related Traffic as a Stressor Eliciting Parental Care in a Roadside-Nesting Bird: The European Bee-Eater Merops apiaster
Traffic is often acknowledged as a threat to biodiversity, but its effects have been mostly
studied on roads subjected to high traffic intensity. The impact of lower traffic intensity such
as those affecting protected areas is generally neglected, but conservation-oriented activities
entailing motorized traffic could paradoxically transform suitable habitats into ecological
traps. Here we questioned whether roadside-nesting bee-eaters Merops apiaster perceived
low traffic intensity as a stressor eliciting risk-avoidance behaviors (alarm calls and flock
flushes) and reducing parental care. Comparisons were established within Doñana
National Park (Spain), between birds exposed to either negligible traffic (ca. 0±10 vehicles
per day) or low traffic intensity (ca. 10±90 vehicles per day) associated to management and
research activities. The frequencies of alarm calls and flock flushes were greater in areas of
higher traffic intensity, which resulted in direct mortality at moderate vehicle speeds ( 40
km/h). Parental feeding rates paralleled changes in traffic intensity, but contrary to our predictions.
Indeed, feeding rates were highest in traffic-exposed nests, during working days
and traffic rush-hours. Traffic-avoidance responses were systematic and likely involved
costs (energy expenditure and mortality), but vehicle transit positively influenced the reproductive
performance of bee-eaters through an increase of nestling feeding rates. Because
the expected outcome of traffic on individual performance can be opposed when responses
are monitored during mating (i.e. negative effect by increase of alarm calls and flock
flushes) or nestling-feeding period (i.e. at least short-term positive effect by increase of nestling
feeding rates), caution should be taken before inferring fitness consequences only
from isolated behaviors or specific life history stages.Peer reviewe
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