The R/V Oceanus completed a 9,789 km, 28 day passage from Woods Hole, Massachusetts, in the Atlantic Ocean, through the Panama Canal to Yaquina Bay, Oregon, in the Pacific Ocean on 21 February 2012. The Oceanus had previously operated in the Mediterranean Sea and Atlantic Ocean (including the Caribbean Sea). We document the sequential acquisition of the barnacles Balanus trigonus and Amphibalanus venustus and the oyster Ostrea equestris on the Oceanus on its high and low latitude transoceanic, intra-oceanic, and interoceanic travels before she was surveyed in Yaquina Bay. The close correspondence between hull fouling accumulations and the detailed two year Oceanus working history reveals B. trigonus settlement occurred in every tropical port visited by the Oceanus, that some populations survived through two of three Woods Hole winters, and that some of these populations passed through the freshwater Panama Canal. These results suggest that marine hull-fouling species are continuously transported globally between most ports of call by most ship passages.
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Benzodiazepines, acting through ionotropic receptors of γ-aminobutyric acid (GABA receptors, GABAR), have been shown to modify feeding behaviour and increase appetite in humans and non-human subjects. However, the cellular and molecular mechanisms that underlie connected short-term behavioural fluctuations are still unclear. In the present study, we used (Prussian carp) as a model organism to research the impact of scantily explored benzodiazepine phenazepam (PNZ) on feeding behaviour and the related molecular mechanisms of PNZ action at single-cell and single-receptor levels. We found that the feeding activity of is under control of GABARs via two distinct mechanisms: orthosteric (triggered by GABA binding site) and allosteric (triggered by benzodiazepine binding site). PNZ displayed clear stimulatory effects on both mechanisms in a GABA-dependent manner. In addition, orthosteric and allosteric effects were found to be partially competitive, which leads to complex behavioural repercussions of conjoint effects of GABAR ligands.
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