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1.
Proc Natl Acad Sci U S A ; 117(12): 6590-6598, 2020 03 24.
Artículo en Inglés | MEDLINE | ID: mdl-32152110

RESUMEN

The effects of predator intimidation on habitat use and behavior of prey species are rarely quantified for large marine vertebrates over ecologically relevant scales. Using state space movement models followed by a series of step selection functions, we analyzed movement data of concurrently tracked prey, bowhead whales (Balaena mysticetus; n = 7), and predator, killer whales (Orcinus orca; n = 3), in a large (63,000 km2), partially ice-covered gulf in the Canadian Arctic. Our analysis revealed pronounced predator-mediated shifts in prey habitat use and behavior over much larger spatiotemporal scales than previously documented in any marine or terrestrial ecosystem. The striking shift from use of open water (predator-free) to dense sea ice and shorelines (predators present) was exhibited gulf-wide by all tracked bowheads during the entire 3-wk period killer whales were present, constituting a nonconsumptive effect (NCE) with unknown energetic or fitness costs. Sea ice is considered quintessential habitat for bowhead whales, and ice-covered areas have frequently been interpreted as preferred bowhead foraging habitat in analyses that have not assessed predator effects. Given the NCEs of apex predators demonstrated here, however, unbiased assessment of habitat use and distribution of bowhead whales and many marine species may not be possible without explicitly incorporating spatiotemporal distribution of predation risk. The apparent use of sea ice as a predator refuge also has implications for how bowhead whales, and likely other ice-associated Arctic marine mammals, will cope with changes in Arctic sea ice dynamics as historically ice-covered areas become increasingly ice-free during summer.


Asunto(s)
Ballena de Groenlandia/fisiología , Ecosistema , Cubierta de Hielo , Orca/fisiología , Animales , Regiones Árticas , Canadá , Biología Marina , Modelos Biológicos , Dinámica Poblacional , Conducta Predatoria
2.
Proc Natl Acad Sci U S A ; 114(10): 2628-2633, 2017 03 07.
Artículo en Inglés | MEDLINE | ID: mdl-28223481

RESUMEN

Although predators influence behavior of prey, analyses of electronic tracking data in marine environments rarely consider how predators affect the behavior of tracked animals. We collected an unprecedented dataset by synchronously tracking predator (killer whales, [Formula: see text] = 1; representing a family group) and prey (narwhal, [Formula: see text] = 7) via satellite telemetry in Admiralty Inlet, a large fjord in the Eastern Canadian Arctic. Analyzing the movement data with a switching-state space model and a series of mixed effects models, we show that the presence of killer whales strongly alters the behavior and distribution of narwhal. When killer whales were present (within about 100 km), narwhal moved closer to shore, where they were presumably less vulnerable. Under predation threat, narwhal movement patterns were more likely to be transiting, whereas in the absence of threat, more likely resident. Effects extended beyond discrete predatory events and persisted steadily for 10 d, the duration that killer whales remained in Admiralty Inlet. Our findings have two key consequences. First, given current reductions in sea ice and increases in Arctic killer whale sightings, killer whales have the potential to reshape Arctic marine mammal distributions and behavior. Second and of more general importance, predators have the potential to strongly affect movement behavior of tracked marine animals. Understanding predator effects may be as or more important than relating movement behavior to resource distribution or bottom-up drivers traditionally included in analyses of marine animal tracking data.


Asunto(s)
Conducta Predatoria/fisiología , Orca/fisiología , Ballenas/fisiología , Animales , Regiones Árticas , Canadá , Ecosistema , Cubierta de Hielo
3.
Toxicol Pathol ; 38(1): 72-5, 2010 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-19884653

RESUMEN

This article summarizes key points from Dr. Bernard Leblanc's presentation European Perspectives on Alternative Mouse Carcinogenicity Models and a distillation of questions and answers from a panel discussion following presentations on Alternative Mouse Models for Carcinogenicity Assessment at the Society of Toxicologic Pathology's annual symposium on June 23, 2009, in Washington, DC.


Asunto(s)
Pruebas de Carcinogenicidad/métodos , Modelos Animales de Enfermedad , Animales , Humanos , Ratones
5.
Toxicol Appl Pharmacol ; 182(3): 188-96, 2002 Aug 01.
Artículo en Inglés | MEDLINE | ID: mdl-12229863

RESUMEN

This report summarizes the deliberations of a multidisciplinary committee, sponsored by the Pharmaceutical Research and Manufacturers of America, on current "best practices" within the U.S. pharmaceutical industry in assessing the role of drug metabolites as potential mediators of the toxicity of new drug products. Input to the document was obtained from numerous sources, including members of the pharmaceutical industry, academic investigators, and representatives of regulatory agencies who attended a workshop on the subject in November 2000. The overall goal of the paper is to define practical and scientifically based approaches to the use of metabolite data that address contemporary issues in the safety evaluation of drug candidates. Although there remains a lack of consensus on how best to deal with several aspects of this complex subject, this paper raises a number of points to consider, which emphasize the need to treat drug metabolite issues on a case-by-case basis. It is hoped that the discussion will promote continued dialog among industrial scientists and regulators charged with ensuring the clinical safety of new therapeutic agents.


Asunto(s)
Ensayos Clínicos como Asunto/normas , Evaluación de Medicamentos/métodos , Industria Farmacéutica/normas , Preparaciones Farmacéuticas/metabolismo , Animales , Evaluación de Medicamentos/normas , Humanos , Preparaciones Farmacéuticas/normas , Pruebas de Toxicidad , Estados Unidos , United States Food and Drug Administration
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