Literatura académica sobre el tema "Silky shark – Behavior"

There is a lack of studies on how provisioning may influence shark numbers and behaviour. The effects of long-term provisioning were investigated at a Red Sea reef, where both grey reef shark (Carcharhinus amblyrhynchos) and silky shark (Carcharhinus falciformis) occurred. Initially, grey reef sharks outnumbered silky sharks, but over 6 years, silky shark numbers increased almost 20-fold, whereas grey-reef sightings decreased >90%. Following this, silky-shark sightings also declined considerably (>80%). It is suggested that these declines could relate to local overfishing. Many silky sharks were identified individually through distinctive markings or conventional tagging. Some individual silky sharks were recorded regularly over 2 years or more, but most appeared to be transient visitors. Sighting records indicated that provisioning extended the residency of transient individuals. If visiting silky sharks were drawn from a larger regional population, this would explain both their initial accumulation and why, to begin with, sightings were sustained despite local fishing pressure. Conversely, the site fidelity typical of grey reef sharks would have made them more susceptible to local depletion. Silky sharks were recorded as behaving more boldly when present in greater numbers, but the decline in grey reef sharks appears to be unrelated to the initial increase in the numbers of silky shark.

Many shark populations are experiencing critical declines from overfishing, triggering potentially detrimental cascade effects on marine ecosystems. Silky sharks, Carcharhinus falciformis, have experienced some of the most severe declines, yet little information exists on their behavioural ecology to inform management decisions. In the present study, the movement patterns of a sexually segregated subpopulation of female silky sharks on reefs in the Central Red Sea were investigated using acoustic telemetry to characterise habitat-use and residency patterns. Frequent baiting of sharks at a particular reef-site significantly increased time spent in the vicinity, although no increases in use of other reef areas 5–10 and 50–60 km away were recorded, and regular use of all three reef areas persisted in the absence of bait. Observed residency patterns varied considerably, from being present almost year-round to visiting only intermittently. The sharks spent significantly longer times at study reefs during daylight hours, even within bait-free regions, suggesting the diel bias is normal. This pattern became less distinct nearer the full moon when there is more ambient light. The regular, perennial use of these reefs by mature and near-mature female silky sharks highlights the importance of this habitat in the Red Sea for recruitment into the local shark population.

Characterizing the vulnerability of both target and non-target (bycatch) species to a fishing gear is a key step towards an ecosystem-based fisheries management approach. This study addresses this issue for the tropical tuna purse seine fishery that uses fish aggregating devices (FADs). We used passive acoustic telemetry to characterize, on a 24 h scale, the associative patterns and the vertical distribution of skipjack (Katsuwonus pelamis), yellowfin (Thunnus albacares), and bigeye tuna (Thunnus obesus) (target species), as well as silky shark (Carcharhinus falciformis), oceanic triggerfish (Canthidermis maculata), and rainbow runner (Elagatis bipinnulata) (major non-target species). Distinct diel associative patterns were observed; the tunas and the silky sharks were more closely associated with FADs during daytime, while the rainbow runner and the oceanic triggerfish were more closely associated during the night. Minor changes in bycatch to catch ratio of rainbow runner and oceanic triggerfish could possibly be achieved by fishing at FADs after sunrise. However, as silky sharks display a similar associative pattern as tunas, no specific change in fishing time could mitigate the vulnerability of this more sensitive species. For the vertical distribution, there was no particular time of the day when any species occurred beyond the depth of a typical purse seine net. While this study does not provide an immediate solution to reduce the bycatch to catch ratios of the FAD-based fishery in the western Indian Ocean, the method described here could be applied to other regions where similar fisheries exist so as to evaluate potential solutions to reducing fishing mortality of non-target species.

There is great concern about the future of sharks in Ecuador because of the lack of biological knowledge of most species that inhabit the region. This paper analyzes the feeding behavior of the pelagic thresher shark (Alopias pelagicus), the blue shark (Prionace glauca) and the silky shark (Carcharhinus falciformis) through the use of stable isotopes of carbon and nitrogen (δ13C and δ15N), with the aim of determining the degree of interaction between these species in the Galapagos Marine Reserve. No interspecific differences were found in use of oceanic vs. inshore feeding areas (δ13C: Kruskal–Wallis test, p = 0.09). The position in the hierarchy of the food web where A. pelagicus feeds differed from that of the other species (δ15N: Kruskal–Wallis test, p = 0.01). There were no significant differences in δ13C and δ15N values between males and females of the three species (Student’s t-test, p > 0.05), which suggests that both sexes have a similar feeding behavior. A specialist strategy was observed in P. glauca (trophic niche breadth TNB = 0.69), while the other species were found to be generalist (A. pelagicus TNB = 1.50 and C. falciformis TNB = 1.09). The estimated trophic level (TL) varied between the three species. C. falciformis occupied the highest trophic level (TL = 4.4), making it a quaternary predator in the region. The results of this study coincide with the identified behavior in these predators in other areas of the tropical Pacific (Colombia and Mexico), and suggest a pelagic foraging strategy with differential consumption of prey between the three species. These ecological aspects can provide timely information when implementing in conservation measures for these shark species in the Tropical Pacific and Galapagos Marine Reserve.

The paired olfactory organs of both the lemon shark (Negaprion brevirostris) and the silky shark (Carcharhinus falciformis) are located in solid cartilaginous nasal capsules, which open at the ventral side of the snout and are entirely separate from the mouth. The olfactory rosette consists of two rows of lamellae arising from a central raphe. The lamellae possess secondary folds covered with sensory epithelium, which contains microvillous receptor cells, supporting cells with both cilia and microvilli, basal cells, and goblet cells. No ciliated receptor cells were found. Gaps between facing lamellae connect the inlet chamber with the outlet chamber. The inlet chamber receives the ventilatory water through the incurrent nostril and the outlet chamber discharges the water through the excurrent nostril. A nasal flap, a septum, and paired valve flaps form an incomplete barrier between incurrent and excurrent nostrils and may have hydrodynamic functions, which are discussed.

The shape of shark teeth varies among species, but traditional testing protocols have revealed no predictive relationship between shark tooth morphology and performance. We developed a dynamic testing device to quantify cutting performance of teeth. We mimicked head-shaking behaviour in feeding large sharks by attaching teeth to the blade of a reciprocating power saw fixed in a custom-built frame. We tested three tooth types at biologically relevant speeds and found differences in tooth cutting ability and wear. Teeth from the bluntnose sixgill ( Hexanchus griseus ) showed poor cutting ability compared with tiger ( Galeocerdo cuvier ), sandbar ( Carcharhinus plumbeus ) and silky ( C. falciformis ) sharks, but they also showed no wear with repeated use. Some shark teeth are very sharp at the expense of quickly dulling, while others are less sharp but dull more slowly. This demonstrates that dynamic testing is vital to understanding the performance of shark teeth.

Silks play an important role in the life of various arthropods. A highly neglected prerequisite to make versatile use of silks is sufficient attachment to substrates. Although there have been some studies on the structure and mechanics of silk anchorages of spiders, for insects only anecdotal reports on attachment-associated spinning behaviour exist. Here, we experimentally studied the silk attachment of the pupae and last instar caterpillars of the tea bagworm Eumeta minuscula (Butler 1881) (Lepidoptera, Psychidae) to the leaves of its host plant Ilex chinensis . We found that the bagworms spin attachment discs, which share some structural features with those of spiders, like a plaque consisting of numerous overlaid, looped glue-coated silk fibres and the medially attaching suspension thread. Although the glue, which coats the fibres, cannot spread and adhere very well to the leaf surface, high pull-off forces were measured, yielding a mean safety factor (force divided by the animal weight) of 385.6. Presumably, the bagworms achieve this by removal of the leaf epidermis prior to silk attachment, which exposes the underlying tissue that represents a much better bonding site. This ensures a reliable attachment during the immobile, vulnerable pupal stage. This is the first study on the biomechanics and structure of silk attachments to substrates in insects.

The silky shark Carcharhinus falciformis forms the primary elasmobranch bycatch in tuna purse seine fisheries using fish aggregating devices (FADs) in all of the world’s tropical oceans. Its life-history traits of slow growth, late maturation and low fecundity make it vulnerable to over exploitation, as is apparent from historical bycatch trends. Very little is known about the associative behaviour of this species with floating objects, information which is essential in formulating effective mitigation and management measures. This study aims to address this knowledge gap through the use of various electronic tagging techniques in conjunction with dietary analysis. Dietary data were collected from 323 silky sharks incidentally caught at FADs. Approximately 40 percent of the diet consisted of prey associated with FADs while the remaining 60 percent were non-associated species of crustaceans, cephalopods and fishes. These results suggest that the associative behaviour is not primarily driven by trophic enhancement, but is likely a combination of predator avoidance, social interactions and feeding. Fine-scale behavioural data from silky sharks associated with drifting FADs were collected through the use of acoustic telemetry techniques. Acoustic tags were implanted into 38 silky sharks (69- 116 cm TL) at eight FADs. FADs were equipped with satellite linked acoustic receivers and abandoned to drift freely. Presence/absence and swimming depth data were telemetered via the Iridium satellite system. A total of 300 d of behavioural data were collected from 20 tagged individuals. Individuals remain associated with the same FAD for extended periods (min = 2.84 d, max = 30.60 d, mean = 15.69 d). Strong diel patterns were observed in both association and swimming depth. Typically individuals moved away from FADs after sunset and return later during the night, then remain closely associated until the following evening. Vertical behaviour also changed around sunset with sharks using fairly constant depths, within the upper 25 m, during the day and switching to rapid vertical movements during the night, with dives in excess of 250 m recoded. Broader scale movement behaviour was investigated using pop-up archival satellite tags (PSATs). Tags were deployed on 46 silky sharks (86-224.5 cm TL) for a total of 1495 d. Light data were used to calculate geolocation estimates and reconstruct the sharks’ trajectories. Movement patterns differed between animals and according to deployment duration. Several extensive horizontal movements were observed, with an average track length of 3240 km during an average tag deployment of 44.02 d. Horizontal movement patterns were found to correlate very closely with drift patterns of FADs. Consequently, it appears that the movement behaviour of juvenile silky sharks is strongly influenced by the movement of drifting FADs in this region. Ghost fishing of silky sharks through entanglement in FADs was also investigated using data derived from PSATs as well as underwater visual censuses. Thirteen per cent of the tagged sharks became entangled in FADs and entangled sharks were observed in 35 percent of the 51 FADs surveyed. Using this information in conjunction with estimated time that sharks remained entangled in the FAD (from depth data from PSATs), and scaling up according to estimates of FAD numbers, it was found that between 480 000 and 960 000 silky sharks are killed annually in this manner in the Indian Ocean. Subsequent management measures in this region prevent the deployment of FADs with netting that could lead to entanglement. Overall, floating objects appear to play a significant role in the juvenile life stages of silky sharks in this region. While their association with floating objects is clearly advantageous in an evolutionary sense, under current tuna fishery trends, this behaviour is certainly detrimental for the population.

The blacknose shark (Carcharhinus acronotus) is a common small coastal shark species found in nearshore waters along the southeast coast of the United States, from North Carolina into the Gulf of Mexico and extending further south into the Bahamas. There has been some debate in recent years over the reproductive periodicity of C. acronotus in waters off the U.S. coast. Earlier studies have suggested that Gulf C. acronotus reproduce on an annual basis whereas the Atlantic populations of this species may reproduce biennially. Additionally, there have been no known studies on the diet of C. acronotus. The goal of the present study was to re-evaluate the reproductive biology of the Atlantic populations of C. acronotus with the intent on clarifying discrepancies in reproduction as well as provide information on dietary trends. This was accomplished by examining male and female reproductive tracts and gut contents in animals caught throughout the Atlantic range of C. acronotus. Based on these data, spermatogenesis occurs between late May to early July with peak sperm production occurring in June and July. In females, follicular development is complete by late June-early July with ovulation occurring shortly afterwards. Mating occurs between mid-June and early July based on the presence of fresh mating scars on females captured during this time. Current data suggests that gestation begins late July with parturition occurring late May to early June the following year. As observed in earlier studies, reproductive periodicity appears to be largely biennial. However, evidence for concurrent follicular development and pregnancy was observed in several females, suggesting that at least a portion of the Atlantic population may reproduce on an annual basis. Dietary data shows a dominance of teleost prey items in the diets of C. acronotus with scianids making up the majority of the identifiable teleosts.