In fish as in other vertebrates, the diverse functions of thyroid hormones are mediated at the peripheral tissue level through iodothyronine deiodinase (dio) enzymes and thyroid hormone receptor (tr) proteins. In this study, we examined thyroid hormone regulation of mRNAs encoding the three deiodinases dio1, dio2 and dio3 - as well as three thyroid hormone receptors trαA, trαB and trβ - in initial phase striped parrotfish (Scarus iseri). Parrotfish were treated with dissolved phase T(3) (20 nM) or methimazole (3 mM) for 3 days. Treatment with exogenous T(3) elevated circulating T(3), while the methimazole treatment depressed plasma T(4). Experimentally-induced hyperthyroidism increased the relative abundance of transcripts encoding trαA and trβ in the liver and brain, but did not affect trαB mRNA levels in either tissue. In both sexes, methimazole-treated fish exhibited elevated dio2 transcripts in the liver and brain, suggesting enhanced outer-ring deiodination activity in these tissues. Accordingly, systemic hyperthyroidism elevated relative dio3 transcript levels in these same tissues. In the gonad, however, patterns of transcript regulation were distinctly different with elevated T(3) increasing mRNAs encoding dio2 in testicular and ovarian tissues and dio3, trαA and trαB in the testes only. Thyroid hormone status did not affect dio1 transcript abundance in the liver, brain or gonads. Taken as a whole, these results demonstrate that thyroidal status influences relative transcript abundance for dio2 and dio3 in the liver, provide new evidence for similar patterns of dio2 and dio3 mRNA regulation in the brain, and make evident that fish exhibit tr subtype-specific transcript abundance changes to altered thyroid status.

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As coral reef ecosystems decline in health worldwide, reef‐associated fishes are being impacted by changes to their coral reef habitats. While previous studies have shown coral reef structure to affect the demography of reef fishes, changes in reef conditions may also impact the behavior of reef fishes as they cope with altered habitats. In this study, we examined spatial patterns of intraspecific behavioral variation in the bicolor damselfish (Stegastes partitus) across the fringing reefs of Curaçao (Caribbean Sea), and explored how this behavioral variation associated with physical and social conditions on the reef. Principal components analysis (PCA) condensed physical parameters of the reef into principal component 1 (PC1), comprising depth, coral cover (%), rugosity, and average hole size (cm2), and principal component 2 (PC2), which represented the number of holes. PC1, but not PC2, increased spatially across the reef as the habitat transitioned from coral rubble in the shallows to live coral on the reef slope. This transition in reef structure was paralleled by changes in social conditions including decreases in bicolor damselfish density in habitats with higher PC1 values. The behavior of bicolor damselfish also varied spatially with greater aggression and more frequent shelter use in habitats with lower PC1 values. Path analysis revealed robust associations between this behavioral variation and physical habitat conditions of the reef, indicating that physical – rather than social – habitat variation is the primary determinant of these spatial patterns of intraspecific behavioral variation. Taken as a whole, this coupling between physical reef structure and behavior suggests that reef fish may show altered behaviors on coral reefs degraded by anthropogenic impacts.

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choriogenins, and estrogen receptor esr1 -but not esr2a -in the liver within 72 hrs, and that these transcriptional changes return to pre-exposure levels within 12 days of the termination of 4-NP or E2 exposure. In sum, these findings validate the use of mRNA levels for several estrogen-responsive genes as accurate biomarkers for short-term 4-NP exposure in the arrow goby. In Chapter 2, I evaluated the effects of 4-NP and E2 exposures on the osmoregulatory ability of C. ios. I exposed adult arrow gobies to 4-NP (10 μg/L or 100 μg/L) or E2 (50 ng/L) for 14 days, and then transferred the fish from a 33 ppt salinity (control) environment to either 20 ppt, or 5 ppt conditions. Whole body water content was then measured, and the relative mRNA levels for the ion channels