LeVY flights are a special class of random walks whose step lengths are not constant but rather are chosen from a probability distribution with a power-law tail. Realizations of Levy flights in physical phenomena are very diverse, examples including fluid dynamics, dynamical systems, and micelles1,2. This diversity raises the possibility that Levy flights may be found in biological systems. A decade ago, it was proposed that Levy flights may be observed in the behaviour of foraging ants3. Recently, it was argued that Drosophila might perform Levy flights4, but the hypothesis that foraging animals in natural environments perform Levy flights has not been tested. Here we study the foraging behaviour of the wandering albatross Diomedea exulans, and find a power-law distribution of flight-time intervals. We interpret our finding of temporal scale invariance in terms of a scale-invariant spatial distribution of food on the ocean surface. Finally, we examine the significance of our finding in relation to the basis of scale-invariant phenomena observed in biological systems.

Lévy flight search patterns of wandering albatrosses

BACKGROUND: Comparing patterns of ter- restrial and marine defaunation helps to place human impacts on marine fauna in context and to navigate toward recovery. De- faunation began in ear- nest tens of thousands of years later in the oceans than it did on land. Al- though defaunation has been less severe in the oceans than on land, our effects on marine animals are increasing in pace and impact. Humans have caused few complete extinctions in the sea, but we are responsible for many ecological, commercial, and local extinctions. Despite our late start, humans have already powerfully changed virtually all major marine ecosystems. ADVANCES: Humans have profoundly de- creased the abundance of both large (e.g., whales) and small (e.g., anchovies) marine fauna. Such declines can generate waves of ecological change that travel both up and down marine food webs and can alter ocean ecosystem functioning. Human harvesters have also been a major force of evolutionary change in the oceans and have reshaped the genetic structure of marine animal popula- tions. Climate change threatens toaccelerate marine defaunation over the next century. The high mobility of many marine animals offers some increased, though limited, ca- pacity for marine species to respond to cli- mate stress, but it also exposes many species to increased risk from other stressors. Be- cause humans are intensely reliant on ocean ecosystems for food and other ecosystem ser- vices, we are deeply affected by all of these forecasted changes. Three lessons emerge when comparing the marine and terrestrial defaunation ex-

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Marine defaunation: Animal loss in the global ocean

1. Carry-over effects occur when processes in one season influence the success of an individual in the following season. This phenomenon has the potential to explain a large amount of variation in individual fitness, but so far has only been described in a limited number of species. This is largely due to difficulties associated with tracking individuals between periods of the annual cycle, but also because of a lack of research specifically designed to examine hypotheses related to carry-over effects. 2. We review the known mechanisms that drive carry-over effects, most notably macronutrient supply, and highlight the types of life histories and ecological situations where we would expect them to most often occur. We also identify a number of other potential mechanisms that require investigation, including micronutrients such as antioxidants. 3. We propose a series of experiments designed to estimate the relative contributions of extrinsic and intrinsic quality effects in the pre-breeding season, which in turn will allow an accurate estimation of the magnitude of carry-over effects. To date this has proven immensely difficult, and we hope that the experimental frameworks described here will stimulate new avenues of research vital to advancing our understanding of how carry-over effects can shape animal life histories. 4. We also explore the potential of state-dependent modelling as a tool for investigating carry-over effects, most notably for its ability to calculate optimal rates of acquisition of a multitude of resources over the course of the annual cycle, and also because it allows us to vary the strength of density-dependent relationships which can alter the magnitude of carry-over effects in either a synergistic or agonistic fashion. 5. In conclusion carry-over effects are likely to be far more widespread than currently indicated, and they are likely to be driven by a multitude of factors including both macro- and micronutrients. For this reason they could feasibly be responsible for a large amount of the observed variation in performance among individuals, and consequently warrant a wealth of new research designed specifically to decompose components of variation in fitness attributes related to processes across and within seasons.

https://besjournals.onlinelibrary.wiley.com/doi/epdf/10.1111/j.1365-2656.2010.01740.x

Carry‐over effects as drivers of fitness differences in animals

Marine fronts at the continental shelves of austral South America: Physical and ecological processes

From basics to clinical: a comprehensive review on spinal cord injury.

In the adult mammalian CNS, chondroitin sulfate proteoglycans (CSPGs) and myelin-associated inhibitors (MAIs) stabilize neuronal structure and restrict compensatory sprouting following injury. The Nogo receptor family members NgR1 and NgR2 bind to MAIs and have been implicated in neuronal inhibition. We found that NgR1 and NgR3 bind with high affinity to the glycosaminoglycan moiety of proteoglycans and participate in CSPG inhibition in cultured neurons. Nogo receptor triple mutants (Ngr1(-/-); Ngr2(-/-); Ngr3(-/-); which are also known as Rtn4r, Rtn4rl2 and Rtn4rl1, respectively), but not single mutants, showed enhanced axonal regeneration following retro-orbital optic nerve crush injury. The combined loss of Ngr1 and Ngr3 (Ngr1(-/-); Ngr3(-/-)), but not Ngr1 and Ngr2 (Ngr1(-/-); Ngr2(-/-)), was sufficient to mimic the triple mutant regeneration phenotype. Regeneration in Ngr1(-/-); Ngr3(-/-) mice was further enhanced by simultaneous ablation of Rptpσ (also known as Ptprs), a known CSPG receptor. Collectively, our results identify NgR1 and NgR3 as CSPG receptors, suggest that there is functional redundancy among CSPG receptors, and provide evidence for shared mechanisms of MAI and CSPG inhibition.

/pdf/ngr1-and-ngr3-are-receptors-for-chondroitin-sulfate-3dlfsdmt58.pdf

NgR1 and NgR3 are receptors for chondroitin sulfate proteoglycans

Giant petrels (Macronectes spp.) are the most sexually dimorphic of all seabirds. We used satellite-tracking and mass change during incubation to investigate the influence of sexual size dimorphism, in terms of the intersexual food competition hypothesis, on foraging and fasting strategies of northern giant petrels at South Georgia. Females foraged at sea whereas males foraged mainly on the South Georgia coast, scavenging on seal and penguin carcasses. Foraging effort (flight speed, distance covered, duration of foraging trips) was greater for females than for males. In contrast, foraging efficiency (proportionate daily mass gain while foraging) was significantly greater for males than for females. Females were significantly closer to the desertion mass threshold than males and could not compensate for the mass loss during the incubation fast while foraging, suggesting greater incubation costs for females than for males. Both sexes regulated the duration and food intake of foraging trips depending on the depletion of the body reserves. In males the total mass gain was best explained by mass at departure and body size. We suggest that sexual segregation of foraging strategies arose from size-related dominance at carcasses, promoting sexual size dimorphism. Our results indicate that sex-specific differences in fasting endurance, contest competition over food and flight metabolic rates are key elements in maintenance of sexual size dimorphism, segregating foraging strategies and presumably reducing competition between sexes.

Sexual dimorphism and sexual segregation in foraging strategies of northern giant petrels, Macronectes halli, during incubation

The movements of two wandering albatrosses, one of each sex, breeding at South Georgia, were tracked using satellite telemetry, particularly to assess whether such birds could be at risk from longline fishing operations in the subtropics. Full details of the performance (number and quality of uplinks) of the Toyocom transmitters are provided, together with data on flight speeds and night and daytime travel by the albatrosses. The female, tracked for seventeen days—covering three foraging trips totalling 13951 km - had a much more northerly distribution than the male, which made two trips to sea during the same period and travelled a minimum distance of 9280 km. On one trip the female frequented the area off Brazil known to be used for longline fisheries. The distributional differences between the sexes support earlier suggestions, based on at-sea observations, that the observed high mortality rates of South Georgian females could be due to a greater likelihood of incidental mortality in longline fishing. These results also show that the presence of females off Brazil can include birds still rearing chicks, rather than simply representing post-breeding dispersal.

Satellite tracking of wandering albatrosses (Diomedea exulans) in the South Atlantic

We develop a new approach to quantifying habitat use within the foraging ranges of satellite-tracked seabirds. We applied kernel estimation techniques to 167 days (3738 locations) of data from Black-browed and Grey-headed albatrosses Diomedea melanophris and D. chrysostoma during the chick-rearing period of the breeding cycle at South Georgia. At this time the activity range of these two species covers an estimated 440 000 and 640 000 km2, respectively, with very substantial overlap. In contrast, kernel estimation reveals that the main foraging areas of these two sympatric, congeneric species are very distinct. Based on location density categories accounting for 50% of locations, the foraging areas cover c. 81 500 and c. 119 700 km2, respectively, with 42% and 50% of the range of one species overlapping with that of the other.

https://www.jstor.org/stable/pdfplus/3677408.pdf

A. G. Wood

Papers

NgR1 and NgR3 are receptors for chondroitin sulfate proteoglycans

Sexual dimorphism and sexual segregation in foraging strategies of northern giant petrels, Macronectes halli, during incubation

Satellite tracking of wandering albatrosses (Diomedea exulans) in the South Atlantic

Quantifying habitat use in satellite-tracked pelagic seabirds : application of kernel estimation to albatross locations

Population dynamics of Black‐browed and Grey‐headed Albatrosses Diomedea melanophris and D. chrysostoma at Bird Island, South Georgia