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The δ15N values of organisms are commonly used across diverse ecosystems to estimate trophic position and infer trophic connectivity. We undertook a novel cross-basin comparison of trophic position in two ecologically well-characterized and different groups of dominant mid-water fish consumers using amino acid nitrogen isotope compositions. We found that trophic positions estimated from the δ15N values of individual amino acids are nearly uniform within both families of these fishes across five global regions despite great variability in bulk tissue δ15N values. Regional differences in the δ15N values of phenylalanine confirmed that bulk tissue δ15N values reflect region-specific water mass biogeochemistry controlling δ15N values at the base of the food web. Trophic positions calculated from amino acid isotopic analyses (AA-TP) for lanternfishes (family Myctophidae) (AA-TP ∼2.9) largely align with expectations from stomach content studies (TP ∼3.2), while AA-TPs for dragonfishes (family Stomiidae) (AA-TP ∼3.2) were lower than TPs derived from stomach content studies (TP∼4.1). We demonstrate that amino acid nitrogen isotope analysis can overcome shortcomings of bulk tissue isotope analysis across biogeochemically distinct systems to provide globally comparative information regarding marine food web structure.

Ammonia oxidation, the first step in nitrification, is performed by certain Beta-and Gammaproteobacteria and Crenarchaea to generate metabolic energy. Ammonia monooxygenase (amoA) genes from both Bacteria and Crenarchaea have been found in a variety of marine ecosystems, but the relative importance of Bacteria versus Crenarchaea in ammonia oxidation is unresolved, and seasonal comparisons are rare. In this study, we compared the abundance of betaproteobacterial and crenarchaeal amoA genes in the coastal Arctic Ocean during summer and winter over 2 years. Summer and winter betaproteobacterial amoA clone libraries were significantly different, although the gene sequences were similar to those found in temperate and polar environments. Betaproteobacterial and crenarchaeal amoA genes were 30-to 115-fold more abundant during the winter than during the summer in both years of the study. Archaeal amoA genes were more abundant than betaproteobacterial amoA genes in the first year, but betaproteobacterial amoA was more abundant than archaeal amoA the following year. The ratio of archaeal amoA gene copies to marine group I crenarchaeal 16S rRNA genes averaged 2.9 over both seasons and years, suggesting that ammonia oxidation was common in Crenarchaea at this location. Potential nitrification rates, as well as the total amoA gene abundance, were highest in the winter when competition with phytoplankton was minimal and ammonium concentrations were the highest. These results suggest that ammonium concentrations were important in determining the rates of ammonia oxidation and the abundance of ammonia-oxidizing Betaproteobacteria and Crenarchaea.

Basalts from the Mid‐Atlantic Ridge change progressively in composition with increasing distance from the Azores platform. Study of the Lucky Strike and Menez Gwen segments reveals much complexity in the gradient. Both segments contain only basalts enriched relative to normal mid‐oceanic ridge basalt, but in two distinct groups. Moderately enriched basalts occur throughout the segments, with proximal Menez Gwen enriched relative to Lucky Strike. Highly enriched basalts occur at segment centers. Incompatible element ratios of the highly enriched basalts exceed those of the Azores platform, while isotopic compositions are less enriched. These observations can be explained by a low‐degree melt of garnet‐bearing Azores mantle added to mantle depleted by previous melt extraction. Melting this “metasomatized” mantle produces lavas that match the enriched samples. The Azores gradient cannot be explained by simple two‐component mixing; rather, it reflects recent melt extraction and addition processes related to southward flow of the Azores plume. The Azores gradient also permits tests of segmentation models. Central supply models predict step functions in chemical compositions between segments. Within‐segment gradients require vertical supply. Central supply is supported by robust central volcanoes, thicker crust at segment centers, and a step function in isotopes between the segments. The lava diversity at segment centers, however, requires batches of distinct magma that are preserved through melting and melt delivery. Within‐segment gradients in moderately incompatible element ratios support a component of multiple supply. The data suggest partial homogenization of magma within a segment and preferential melt focusing to segment centers with some vertical transport.

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