Trace elements were analyzed in fish of commercial interest to determine their importance in marine systems of the Western Indian Ocean and their bioaccumulation patterns. The results are equivalent or lower than levels reported in ichthyofauna worldwide. Certain values of muscular Cd, Hg, Pb and Zn were however above thresholds for human consumption. Levels varied among tissues, species and with fish length, but were seldom influenced by the nutritional condition of the fish, its gender and its reproductive status. Correlations between hepatic Hg and Se levels in Swordfish (r 2 = 0.747) and Yellowfin Tunas (r 2 = 0.226), and among metallothionein linking metals imply the existence of detoxification processes in these species. Differences in levels between fish from the Mozambique Channel and Reunion Island probably reflect differences of diets rather than differences of elemental availability in both environments.Capsule : Metal bioaccumulation was quantified in four species of pelagic fish.

Artificial lights at night cause high mortality of seabirds, one of the most endangered groups of birds globally. Fledglings of burrow-nesting seabirds, and to a lesser extent adults, are attracted to and then grounded (i.e., forced to land) by lights when they fly at night. We reviewed the current state of knowledge of seabird attraction to light to identify information gaps and propose measures to address the problem. Although species in families such as Alcidae and Anatidae can be grounded by artificial light, the most affected seabirds are petrels and shearwaters (Procellariiformes). At least 56 species of Procellariiformes, more than one-third of them (24) threatened, are subject to grounding by lights. Seabirds grounded by lights have been found worldwide, mainly on oceanic islands but also at some continental locations. Petrel breeding grounds confined to formerly uninhabited islands are particularly at risk from light pollution due to tourism and urban sprawl. Where it is impractical to ban external lights, rescue programs of grounded birds offer the most immediate and employed mitigation to reduce the rate of light-induced mortality and save thousands of birds every year. These programs also provide useful information for seabird management. However, these data are typically fragmentary, biased, and uncertain and can lead to inaccurate impact estimates and poor understanding of the phenomenon of seabird attraction to lights. We believe the most urgently needed actions to mitigate and understand light-induced mortality of seabirds are estimation of mortality and effects on populations; determination of threshold light levels and safe distances from light sources; documentation of the fate of rescued birds; improvement of rescue campaigns, particularly in terms of increasing recovery rates and level of care; and research on seabird-friendly lights to reduce attraction.

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Shearwaters and petrels (hereafter petrels) are highly adapted seabirds that occur across all the world's oceans. Petrels are a threatened seabird group comprising 124 species. They have bet-hedging life histories typified by extended chick rearing periods, low fecundity, high adult survival, strong philopatry, monogamy and long-term mate fidelity and are thus vulnerable to change. Anthropogenic alterations on land and at sea have led to a poor conservation status of many petrels with 52 (42%) threatened

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The foraging behaviour of animals depends on the distribution, abundance and predictability of their food resources. In the marine environment, top predators such as seabirds are known to concentrate their foraging effort in specific oceanic features where productivity is elevated or prey concentrated. When marine productivity is low and prey distribution unpredictable, such as in tropical waters, selection should favour the evolution of flexible foraging strategies. By using GPS, Argos transmitters and activity recorders, we studied the foraging strategy of red-footed boobies (RFBs) Sula sula breeding on Europa Island in the Mozambique Channel, to examine the way a central place forager searches for prey in tropical waters. RFBs only foraged during the day-time and never sat on the water at night; thus, they consequently had a limited maximum foraging range of 148 km. Primary production within this range was low overall (average 0.165 mg chlorophyll m -3 ), with a high spatial and temporal heterogeneity due to the presence of strong geostrophic currents and surface mixing by storms. RFBs appear to adjust their foraging strategy to cope with this situation. Individual birds do not return to the same oceanic sites from one trip to the next, but generally head in the direction of zones where productivity is enhanced. Active foraging, i.e. periods when birds spent time on the sea surface or dived, occurred at the most distant part of the foraging trip. Despite their limited foraging range and the low productivity of surrounding waters, red-footed boobies are able to track zones of prey availability located in areas of enhanced primary production. Searching is probably favoured by the presence of sub-surface predators that chase prey to the surface. The foraging strategy of this tropical sulid appears to differ extensively from that of temperate or polar seabirds whose prey distribution and availability are more predictable.

Most hypotheses attempting to explain the evolution of reversed sexual dimorphism (RSD) assume that size-related differences in foraging ability are of prime importance, but the studies on sex-specific differences in foraging behaviour remain scarce. We compare the foraging behaviour of males and females in a seabird species with a RSD by using several miniaturised activity and telemetry loggers. In red-footed boobies males are 5% smaller and 15% lighter than females, but have a longer tail than females. Both sexes spend similar time on the nest while incubating or brooding. When foraging at sea, males and females spend similar time foraging in oceanic waters, forage in similar areas, spend similar proportion of their foraging trip in flight, and feed on similar prey-flying fishes and flying squids-of similar size. However, compared to males, females range farther during incubation (85 km vs. 50 km), and furthermore feed mostly at the extremity of their foraging trip, whereas males actively forage throughout the trip. Males are much more active than females, landing and diving more often. During the study period, males lost mass, whereas females showed no significant changes. These results indicate that males and females of the red-footed boobies differ in several aspects in their foraging behaviour. Although some differences found in the study may be the direct result of the larger size of females, that is, the slightly higher speeds and deeper depths attained by females, others indicate clearly different foraging strategies between the sexes. The smaller size and longer tail of males confer them a higher agility, and could allow them to occupy a foraging niche different from that of females. The higher foraging effort of males related to its different foraging strategy is probably at the origin of the rapid mass loss of males during the breeding period. These results suggest that foraging differences are probably the reason for the differential breeding investment observed in boobies, and are likely to be involved in the evolution and maintenance of RSD.

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