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Abstract Abundance, biomass, size and distribution of macro-jellyfish were measured in the Northern Gulf of Alaska (NGA). Nearly 1000 kg dispersed among ~13 800 jellyfish were collected using a 5-m2 Methot net. We present length-weight regressions for seven most-common taxa. Catches were dominated by the hydrozoan Aequorea victoria and the scyphozoan Chrysaora melanaster. During 2018, epipelagic macro-jellyfish biomass averaged 1.46 ± 0.36 g WW m−3 for July and 1.14 ± 0.23 g WW m−3 for September, while during 2019 they averaged 0.86 ± 0.19 g WW m−3 for July and 0.72 ± 0.21 g WW m−3 by September. Despite similar biomass among seasons within a year, July abundances were fivefold greater than abundances in September, with July catches dominated by smaller-sized jellyfish over the inner shelf, while during September larger jellyfish were more prominent and most predominant at offshore stations. Comparison to 20 years of data from standard towed nets allowed determination of the relative magnitude of the dominant carnivorous zooplankton components: scyphozoans, hydrozoans and chaetognaths in the NGA. The biomass of these smaller epipelagic predators (5.4 mg WW m−3 for hydrozoans and 10.5 mg WW m−3 for chaetognaths) is a low percentage of the macro-jellyfish, despite their much higher numerical abundance. 

Abstract A 25‐year (1996–2020) hindcast from a coupled physical‐biogeochemical model is evaluated with nutrients, phytoplankton and zooplankton field data and is analyzed to identify mechanisms controlling seasonal and interannual variability of the northern Gulf of Alaska (NGA) planktonic food web. Characterized by a mosaic of processes, the NGA is a biologically complex and productive marine ecosystem. Empirical Orthogonal Function (EOF) analysis combining abiotic and biotic variables averaged over the continental shelf reveals that light intensity is a main driver for nanophytoplankton variability during spring, and that nitrate availability is a main driver for diatoms during spring and for both phytoplankton during summer. Zooplankton variability is a combination of carry‐over effects from the previous year and bottom‐up controls from the current year, with copepods and euphausiids responding to diatoms and microzooplankton responding to nanophytoplankton. The results also demonstrate the effect of nitrate availability and phytoplankton community structure on changes in biomass and energy transfers across the planktonic food web over the entire growing season. In particular, the biomass of large copepods and euphausiids increases more significantly during years of higher relative diatom abundance, as opposed to years with higher nitrate availability. Large microzooplankton was identified as the planktonic group most sensitive to perturbations, presumably due to its central position in the food web. By quantifying the combined variability of several key planktonic functional groups over a 25‐year period, this work lays the foundation for an improved understanding of the long‐term impacts of climate change on the NGA shelf. 

Abstract BackgroundDiapause is a seasonal dormancy that allows organisms to survive unfavorable conditions and optimizes the timing of reproduction and growth. Emergence from diapause reverses the state of arrested development and metabolic suppression returning the organism to an active state. The physiological mechanisms that regulate the transition from diapause to post-diapause are still unknown. In this study, this transition has been characterized for the sub-arctic calanoid copepodNeocalanus flemingeri, a key crustacean zooplankter that supports the highly productive North Pacific fisheries. Transcriptional profiling of females, determined over a two-week time series starting with diapausing females collected from > 400 m depth, characterized the molecular mechanisms that regulate the post-diapause trajectory. ResultsA complex set of transitions in relative gene expression defined the transcriptomic changes from diapause to post-diapause. Despite low temperatures (5–6 °C), the switch from a “diapause” to a “post-diapause” transcriptional profile occurred within 12 h of the termination stimulus. Transcriptional changes signaling the end of diapause were activated within one-hour post collection and included the up-regulation of genes involved in the 20E cascade pathway, the TCA cycle and RNA metabolism in combination with the down-regulation of genes associated with chromatin silencing. By 12 h, females exhibited a post-diapause phenotype characterized by the up-regulation of genes involved in cell division, cell differentiation and multiple developmental processes. By seven days post collection, the reproductive program was fully activated as indicated by up-regulation of genes involved in oogenesis and energy metabolism, processes that were enriched among the differentially expressed genes. ConclusionsThe analysis revealed a finely structured, precisely orchestrated sequence of transcriptional changes that led to rapid changes in the activation of biological processes paving the way to the successful completion of the reproductive program. Our findings lead to new hypotheses related to potentially universal mechanisms that terminate diapause before an organism can resume its developmental program.