136 research outputs found
Reevaluation of patterns of mussel (Mytilus edulis) selection by European Oystercatchers (Haematopus ostralegus)
© National Research Council of Canada 2002. Published version reproduced with the permission of the publisher.European Oystercatchers (Haematopus ostralegus) were highly selective towards mussels between 35 and 50 mm in length, and fewer than 5% of mussels taken were below 35 mm or above 50 mm. The oystercatchers selected ventrally thin-shelled mussels, especially if the length was more than 35 mm, regardless of whether they opened the right or left valve of the mussel. The oystercatchers also took mussels that had few barnacles on the ventral surface. Although brown-shelled mussels were rare in the population, oystercatchers showed a strong preference for them. Generally, oystercatchers consumed ventrally flat mussels, especially in the smaller length classes, particularly the most preferred size class, 30–45 mm. Ventral shell thickness and colour had independent effects on mussel selection. The other two variables, number of barnacles and shape of the ventral surface (flat or curved), apparently had no influence on selection on their own, only by way of their association with colour or thickness
Life path analysis: scaling indicates priming effects of social and habitat factors on dispersal distances
1. Movements of many animals along a life-path can be separated into repetitive ones within home ranges and transitions between home ranges. We sought relationships of social and environmental factors with initiation and distance of transition movements in 114 buzzards Buteo buteo that were marked as nestlings with long-life radio tags.
2. Ex-natal dispersal movements of 51 buzzards in autumn were longer than for 30 later in their first year and than 35 extra-natal movements between home ranges after leaving nest areas. In the second and third springs, distances moved from winter focal points by birds that paired were the same or less than for unpaired birds. No post-nuptial movement exceeded 2 km.
3. Initiation of early ex-natal dispersal was enhanced by presence of many sibs, but also by lack of worm-rich loam soils. Distances travelled were greatest for birds from small broods and with relatively little short grass-feeding habitat near the nest. Later movements were generally enhanced by the absence of loam soils and short grassland, especially with abundance of other buzzards and probable poor feeding habitats (heathland, long grass).
4. Buzzards tended to persist in their first autumn where arable land was abundant, but subsequently showed a strong tendency to move from this habitat.
5. Factors that acted most strongly in ½-km buffers round nests, or round subsequent focal points, usually promoted movement compared with factors acting at a larger scale. Strong relationships between movement distances and environmental characteristics in ½-km buffers, especially during early ex-natal dispersal, suggested that buzzards became primed by these factors to travel far.
6. Movements were also farthest for buzzards that had already moved far from their natal nests, perhaps reflecting genetic predisposition, long-term priming or poor habitat beyond the study area
Population overlap and habitat segregation in wintering Black-tailed Godwits Limosa limosa
Distinct breeding populations of migratory species may overlap both spatially and temporally, but differ in patterns of habitat use. This has important implications for population monitoring and conservation. To quantify the extent to which two distinct breeding populations of a migratory shorebird, the Black-tailed Godwit Limosa limosa, overlap spatially, temporally and in their use of different habitats during winter. We use mid-winter counts between 1990 and 2001 to identify the most important sites in Iberia for Black-tailed Godwits. Monthly surveys of estuarine mudflats and rice-fields at one major site, the Tejo estuary in Portugal in 2005-2007, together with detailed tracking of colour-ringed individuals, are used to explore patterns of habitat use and segregation of the Icelandic subspecies L. l. islandica and the nominate continental subspecies L. l. limosa. In the period 1990-2001, over 66 000 Black-tailed Godwits were counted on average in Iberia during mid-winter (January), of which 80% occurred at just four sites: Tejo and Sado lower basins in Portugal, and Coto Dontildeana and Ebro Delta in Spain. Icelandic Black-tailed Godwits are present throughout the winter and forage primarily in estuarine habitats. Continental Black-tailed Godwits are present from December to March and primarily use rice-fields. Iberia supports about 30% of the Icelandic population in winter and most of the continental population during spring passage. While the Icelandic population is currently increasing, the continental population is declining rapidly. Although the estuarine habitats used by Icelandic godwits are largely protected as Natura 2000 sites, the habitat segregation means that conservation actions for the decreasing numbers of continental godwits should focus on protection of rice-fields and re-establishment of freshwater wetlands
A Review of Flight-Initiation Distances and their Application to Managing Disturbance to Australian Birds
Disturbance – the response of birds to a stimulus such as the presence of a person – is considered a conservation threat for some Australian birds. The distance at which a bird flees from perceived danger is defined as the flight-initiation distance (FID), and could be used to designate separation distances between birds and stimuli that might cause disturbance. We review the known FIDs for Australian birds, and report FIDs for 250 species. Most FIDs are from south-eastern Australia, and almost all refer to a single walker as the stimulus. Several prominent factors correlated with FID are discussed (e.g. body mass and the distance at which an approach begins). FIDs have not been used extensively in the management of disturbance, for a variety of reasons including lack and inaccessibility of available data. We call for standardised data collection and greater application of available data to the management of disturbance
Pacing and Decision Making in Sport and Exercise: The Roles of Perception and Action in the Regulation of Exercise Intensity
In pursuit of optimal performance, athletes and physical exercisers alike have to make decisions about how and when to invest their energy. The process of pacing has been associated with the goal-directed regulation of exercise intensity across an exercise bout. The current review explores divergent views on understanding underlying mechanisms of decision making in pacing. Current pacing literature provides a wide range of aspects that might be involved in the determination of an athlete's pacing strategy, but lacks in explaining how perception and action are coupled in establishing behaviour. In contrast, decision-making literature rooted in the understanding that perception and action are coupled provides refreshing perspectives on explaining the mechanisms that underlie natural interactive behaviour. Contrary to the assumption of behaviour that is managed by a higher-order governor that passively constructs internal representations of the world, an ecological approach is considered. According to this approach, knowledge is rooted in the direct experience of meaningful environmental objects and events in individual environmental processes. To assist a neuropsychological explanation of decision making in exercise regulation, the relevance of the affordance competition hypothesis is explored. By considering pacing as a behavioural expression of continuous decision making, new insights on underlying mechanisms in pacing and optimal performance can be developed. © 2014 Springer International Publishing Switzerland
Ecological impacts of non-native Pacific oysters (Crassostrea gigas) and management measures for protected areas in Europe
Pacific oysters are now one of the most ‘globalised’ marine invertebrates. They dominate bivalve aquaculture production in many regions and wild populations are increasingly becoming established, with potential to displace native species and modify habitats and ecosystems. While some fishing communities may benefit from wild populations, there is now a tension between the continued production of Pacific oysters and risk to biodiversity, which is of particular concern within protected sites. The issue of the Pacific oyster therefore locates at the intersection between two policy areas: one concerning the conservation of protected habitats, the other relating to livelihoods and the socio-economics of coastal aquaculture and fishing communities. To help provide an informed basis for management decisions, we first summarise evidence for ecological impacts of wild Pacific oysters in representative coastal habitats. At local scales, it is clear that establishment of Pacific oysters can significantly alter diversity, community structure and ecosystem processes, with effects varying among habitats and locations and with the density of oysters. Less evidence is available to evaluate regional-scale impacts. A range of management measures have been applied to mitigate negative impacts of wild Pacific oysters and we develop recommendations which are consistent with the scientific evidence and believe compatible with multiple interests. We conclude that all stakeholders must engage in regional decision making to help minimise negative environmental impacts, and promote sustainable industry development
Predation risk and foraging behavior of the hoary marmot in Alaska
I observed hoary marmots for three field seasons to determine how the distribution of food and the risk of predation influenced marmots' foraging behavior. I quantified the amount of time Marmota caligata foraged in different patches of alpine meadows and assessed the distribution and abundance of vegetation eaten by marmots in these meadows. Because marmots dig burrows and run to them when attacked by predators, marmot-toburrow distance provided an index of predation risk that could be specified for different meadow patches.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/46873/1/265_2004_Article_BF00292992.pd
The concept of carrying capacity and shorebirds
This paper discusses the term 'carrying capacity, defined in terms of the 'one-in, one-out rule'. On this definition, capacity is reached when, for every additional bird that arrives, another one either dies or emigrates, so that numbers in a locality cannot increase and the habitat is fully occupied. Simulations with an individuals-based and physiologically structured model showed that this definition is appropriate for wintering oystercatchers eating mussels, a system in which interference between foraging birds occurs; as the numbers of recruits settling on the mussel beds in September increased to very high levels, the number remaining by spring reached a plateau. Whether birds were assumed to remain on the estuary until they died at some point during the winter or whether they emigrated before they starved made no difference to the predicted capacity of the mussel beds. Carrying capacity in this system could also be defined in terms of the total bird-days per winter because this quantity likewise tended to plateau as the numbers of recruits settling in September increased. However, the plateau was less clearly defined and it took a very much higher number of September recruits for capacity defined this way to be reached.
Further simulations showed that, without interference, the numbers of autumn recruits could be increased to the point at which no birds remained on the mussel beds by spring because food density had been depleted to below the levels required for even the most efficient birds to balance their energy budget. The relationship between numbers remaining by March and the numbers settling the previous September was thus dome-shaped. In systems with little or no interference, therefore, carrying capacity may only be measured as the total number of bird-days depends critically on the numbers of birds that arrive in September. Defining carrying capacity in terms of bird-days per winter rather than in terms of the numbers remaining in March does not solve the difficulties of defining and measuring capacity in systems without interference. In such systems, measuring capacity in bird-days per winter — as is so often done — provides a poor prediction because the total number of bird-days depends on the numbers that arrive in autumn.
Whether carrying capacity is actually reached depends on there being a sufficiently large number of potential recruits to the estuary in autumn; in the oystercatcher— mussel system, it required 8000 recruits in September for the carrying capacity of ca 320 to be achieved. In many species and localities there may not normally enough recruits fo e capacity of a locality to be reached. However this should not be taken to mean that a reduction in food supplies through habitat loss or change would not affect
local numbers If competition for food is sufficiently intense or the rates of emigration and/or mortality to be density-dependentyouo increased , a reduction in the food suppl ld lead t ' rates of emigration and/or mortality, and so to a reduction in local bird numbers. This was confirmed by simulations which showed that winter habitat loss used local mortality or emigration to increase in oystercatchers long before carrying capacity was reached
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