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1.
Adv Exp Med Biol ; 875: 815-20, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-26611037

RESUMO

Anthropogenic noise is a by-product from human activity that impacts protected species and is increasingly being considered in environmental management decisions. Offshore energy development presents a navigational hazard to existing shipping, making the locations of these two sources of noise mutually exclusive. This fact means that licensing decisions are stepping into the realm of coastal and marine spatial planning (CMSP). To be effective, conservation measures must also be considered in the CMSP process to mitigate potential cumulative adverse effects associated with resource development, particularly with multiuse conflicts. Thus managers should consider shipping lane relocation to make environmentally optimal decisions.


Assuntos
Conservação dos Recursos Naturais , Ecossistema , Navios , Ruído
2.
Mar Pollut Bull ; 85(1): 24-32, 2014 Aug 15.
Artigo em Inglês | MEDLINE | ID: mdl-24998798

RESUMO

The North Atlantic right whale (Eubalaena glacialis) faces increasing pressure from commercial shipping traffic and proposed marine renewable energy developments. Drawing upon the successful Stellwagen Bank National Marine Sanctuary model, we propose a multi-stakeholder marine spatial planning process that considers both appropriate positioning of offshore wind farms and redefining commercial shipping lanes relative to whale migration routes: placement of wind turbines within certain right whale habitats may prove beneficial for the species. To that end, it may be advisable to initially relocate the shipping lanes for the benefit of the whales prior to selecting wind energy areas. The optimal end-state is the commercial viability of renewable energy, as well as a safe shipping infrastructure, with minimal risk of collision and exposure to shipping noise for the whales. This opportunity to manage impacts on right whales could serve as a model for other problematic interactions between marine life and commercial activities.


Assuntos
Cooperação Internacional , Baleias/fisiologia , Migração Animal , Animais , Oceano Atlântico , Ecossistema , Monitoramento Ambiental/métodos , Geografia , Ruído , Energia Renovável , Navios , Meios de Transporte , Vento
3.
Brain Res ; 1358: 89-101, 2010 Oct 28.
Artigo em Inglês | MEDLINE | ID: mdl-20728435

RESUMO

Estrogens affect body fluid balance, including sodium ingestion. Recent findings of a population of neurons in the hindbrain nucleus of the solitary tract (NTS) of rats that are activated during sodium need suggest a possible central substrate for this effect of estrogens. We used immunohistochemistry to label neurons in the NTS that express 11-ß-hydroxysteroid dehydrogenase type 2 (HSD2), an enzyme that promotes aldosterone binding, in male rats, and in ovariectomized (OVX) rats given estradiol benzoate (EB) or oil vehicle (OIL). During baseline conditions, the number of HSD2 immunoreactive neurons in the NTS immediately rostral to the area postrema was greater in EB-treated OVX rats compared to those in OIL-treated OVX and male rats. A small number of HSD2 immunoreactive neurons was also labeled for dopamine-ß-hydroxylase (DBH), an enzyme involved in norepinephrine biosynthesis. Double-labeled neurons in the NTS were located primarily in the more lateral portion of the HSD2 population, at the level of the area postrema in all three groups, with no sex or estrogen-mediated differences in the number of double-labeled neurons. These results suggest that two subpopulations of HSD2 neurons are present in the NTS. One subpopulation, which does not colocalize with DBH and is increased during conditions of elevated estradiol, may contribute to the effects of estrogens on sodium ingestion. The role of the other, smaller subpopulation, which colocalizes with DBH and is not affected by estradiol, remains to be determined, but one possibility is that these latter neurons are part of a larger network of catecholaminergic input to neuroendocrine neurons in the hypothalamus.


Assuntos
11-beta-Hidroxiesteroide Desidrogenase Tipo 2/metabolismo , Anticoncepcionais/farmacologia , Estradiol/análogos & derivados , Neurônios/efeitos dos fármacos , Neurônios/metabolismo , Núcleo Solitário/citologia , Animais , Peso Corporal/efeitos dos fármacos , Contagem de Células/instrumentação , Dopamina beta-Hidroxilase/metabolismo , Estradiol/farmacologia , Feminino , Tamanho do Órgão/efeitos dos fármacos , Ovariectomia/métodos , Ratos , Ratos Sprague-Dawley , Ureter/anatomia & histologia , Ureter/efeitos dos fármacos
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