We surveyed offshore fish populations in the Gulf of Mexico in 2011 and 2012, following persistent reports of abnormal skin lesions and other pathologies in the aftermath of the Deepwater Horizon oil spill. The incidence of skin lesions in 2011 sampling was most frequent in some bottom‐dwelling species along the continental shelf edge north of the Deepwater Horizon site. Longline surveys revealed that by 2012 the overall frequency of lesions in northern Gulf of Mexico (NGM) fishes in the vicinity of the Deepwater Horizon had declined 53%, with severity also declining. Relatively high concentrations of polycyclic aromatic hydrocarbon (PAH) metabolites (up to 470,000 ng naphthalene equivalents/g bile wet weight), indicative of oil‐related pollution, were found in fish bile in 2011; concentrations of summed PAHs measured in fish liver and muscle were relatively low (<35 ng/g) due to the efficient metabolism of these compounds by teleost fish. Significant declines in bile concentrations of naphthalene and phenanthrene metabolites in Red Snapper Lutjanus campechanus between 2011 and 2012 indicate an episodic exposure to elevated levels of hydrocarbons of petrogenic origin. The composition of PAH parent compounds and alkylated homologs in Red Snapper liver samples was highly correlated with oil collected at the Deepwater Horizon wellhead but was less coherent with other PAH sources in the NGM. The elevated 2011 prevalence of skin lesions in some NGM species was unrelated to surface salinity or temperature anomalies and was not the result of an epizootic observable in our histopathology samples but was positively correlated with PAH concentration. Thus, we fail to reject the null hypothesis that elevated skin lesion frequency is unrelated to PAH exposure from the Deepwater Horizon oil spill. Received August 14, 2013; accepted March 26, 2014

Microchemical analyses of fish otoliths have revolutionized fisheries science. Molecules deposited within otoliths may originate from ambient water and diet, with molecular concentrations being subject to subsequent physiological alteration after exposure. Analyses of otolith microstructure and incorporation of inorganic elements have led to major advances in stock assessment and fisheries ecology. However, the use of otoliths for microchemical analyses has drawbacks. Specifically, otolith removal from live specimens requires specimen sacrifice, which may be forbidden in the case of protected species. In addition, otoliths rarely contain sufficient concentrations of organic matter to allow reconstruction of food-web relationships via multiple stable isotopes, and otolith microstructure can be difficult to interpret in some species. Here, we review alternatives to otoliths that can provide microchemical analytes for life-history studies in fishes. Our focus is to describe advantages and disadvantages to the use of each alternative structure, with particular attention paid to trace-element analysis for inorganic matrices and stable-isotope analysis for organic ones. In general, the chronological analysis of elemental and isotopic values within each structure depends on the inert nature (or lack of molecular turnover) of the tissue. Structures with high turnover rates or those that are metabolically active will not effectively record elemental or isotopic compositions over time. Here, we provide an assessment of the use of bony endoskeleton, fin spines, fin rays, scales, and eye lenses as alternatives or complements to fish otolith analysis.

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We evaluated eye lenses as potential recorders of stable isotope histories in fish because they consist of metabolically inert optical proteins that are deposited in successive, concentric circles (laminae) much like otolith circuli and tree rings. We conducted four different tests on lenses from red snapper, red grouper, gag, and white grunt. The first test was a low-resolution screening of multiple individuals (4–5 radial groups of laminae per lens, all species except white grunt). Along the radial axis, all individuals exhibited substantial isotopic variability. Red snapper individuals separated into two groups based on δ 15N and gag separated into two groups based on δ 13C. Two gag with the greatest variation were chosen for high-resolution temporal analysis using individual laminae from their second eye lenses. The first-order patterns from the high-resolution analysis generally mimicked patterns from the low-resolution screening of grouped laminae, yet the high-resolution plots revealed early-life details that were not apparent in the low-resolution screenings. For the third test, left- versus right-eye variation was compared using high-resolution methods. White grunt left- and right-eye radial isotopic patterns were almost identical for both δ 13C and δ 15N, suggesting the variations observed among individual fish were not artifacts. The final test evaluated intra-laminar variation; multiple samples were analyzed from different parts of the same lamina. Seven laminae from three individuals of two species were analyzed in this manner; variations among laminae were found to be much higher than variations within laminae. However, nominal intra-laminar variations were comparable to nominal differences between left and right lenses, suggesting intra-laminar variation established measurement precision. Eye lens isotopes appear to be useful for reconstructing the isotopic histories of individual fish; these histories can be compared with spatially-derived isoscapes to reconstruct individual histories for site fidelity, movement and trophic position.

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