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In this letter, we introduce The Polar Vocabularies and Semantics Working Group, originally established as a joint effort between the joint SAON/IASC Arctic Data Committee and the Data Management Collaboration Team of the Interagency Arctic Research Policy Committee. We Invite, communities of practice to actively engage with us in our activities (described below), to advance the state of semantics-based applications in polar activities (and to increase interoperability between stakeholders and rights holders within existing and emerging digital ecosystems).

cti_cross_region_taxon This repository provides the data and codes used in the manuscript: Guillem Chust, Ernesto Villarino, Matthew McLean, Nova Mieszkowska, Lisandro Benedetti-Cecchi, Fabio Bulleri, Chiara Ravaglioli, Angel Borja, Iñigo Muxika, José A. Fernandes-Salvador, Leire Ibaibarriaga, Ainhize Uriarte, Marta Revilla, Fernando Villate, Arantza Iriarte, Ibon Uriarte, Soultana Zervoudaki, Jacob Carstensen, Paul J. Somerfield, Ana M. Queirós , Andrea J. McEvoy, Arnaud Auber, Manuel Hidalgo, Marta Coll, Joaquim Garrabou, Daniel Gómez-Gras, Cristina Linares, Francisco Ramírez, Núria Margarit, Mario Lepage, Chloé Dambrine, Jérémy Lobry, Myron A. Peck, Paula de la Barra, Anieke van Leeuwen, Gil Rilov, Erez Yeruham, Anik Brind'Amour, and Martin Lindegren. Cross-basin and cross-taxa patterns of marine community tropicalization and deborealization in warming European seas. Nature Communications Please check the github repo cti_cross_region_taxon for updates. Abstract Ocean warming and acidification, decreases in dissolved oxygen concentrations, and changes in primary production are causing an unprecedented global redistribution of marine life. The identification of underlying ecological processes underpinning marine species turnover, particularly the prevalence of tropicalization over deborealization, has been recently debated in the context of ocean warming. Here, we track changes in the mean thermal affinity of marine communities across European seas by calculating the Community Temperature Index for 65 biodiversity time series collected over four decades and containing 1,817 species from different communities (zooplankton, coastal benthos, pelagic and demersal invertebrates and fish). We show most communities and sites have clearly responded to ongoing ocean warming via abundance increases of warm-water species (tropicalization; 54%) and decreases of cold-water species (deborealization; 18%). Tropicalization dominated Atlantic sites compared to semi-enclosed basins such as the Mediterranean and Baltic Seas, probably due to physical barrier constraints to connectivity and species colonization. Semi-enclosed basins appeared to be particularly vulnerable to ocean warming, experiencing the fastest rates of warming and biodiversity loss through deborealization. Keywords: climate change, community temperature index, CTI, ocean connectivity. Acknowledgements This study has been supported by the European Union's Horizon 2020 research and innovation programme under grant agreement No 869300 (FutureMARES project) (G.C., E.V., J.F-S., M.P., M.Lin., C.D., D.G-G., G.R., L.B., C.R., M.C., F.R., G.R., P.B., M.P., M.Lep., J.L., A.B., N.M., J.G., F.B., L.B.C, A.Q., F.V., A.I., and I.U.), and by the Urban Klima 2050 -- LIFE 18 IPC 000001 project, which has been received funding from European Union's LIFE programme (G.C., E.V., L.I., A.B., A.U., and M.R.). Additional financial support was obtained from the Basque Government (PIBA2020-1-0028 & IT1723-22). We thank the NOAA Climate Prediction Center for providing Sea Temperature data through the NCEP Global Ocean Data Assimilation System (GODAS) www.cpc.ncep.noaa.gov/products/GODAS. We also thank Ocean Biodiversity Information System (OBIS) for providing global occurrences of the biological group studied here. Data from the Basque Country were obtained from the Basque Water Agency (URA) monitoring network, through a Convention with AZTI. M.C., J.G., D.G.-G. and F.R. acknowledge the 'Severo Ochoa Centre of Excellence' accreditation (CEX2019-000928-S). Authors M.H. and M.Lin. are grateful for the support from ICES Working Group on Comparative Ecosystem-based Analyses of Atlantic and Mediterranean marine systems (WGCOMEDA) for this research. This paper is contribution nº xxxx from AZTI, Marine Research, Basque Research and Technology Alliance (BRTA)

The repository contains the version of PISCES that was used to investigate the role played by low latitudes and the Southern Ocean at sustaining export production and PP in the low latitudes. This code is based on version 3.6 of NEMO and the repository only includes routines that have been changed with respect to this version. The code is in Fortran 90.

Anvi'o databases of the 47 ammonia-oxidizing archaea MAGs from abyssal and hadal surface sediments presented in Trouche et al, 2023 (https://doi.org/10.1038/s43705-023-00341-6). 

The uploaded file contains three separate Python scripts aimed at modeling the sinking velocity of natural Trichodesmium colonies loaded with dust particles. Two scripts have been developed to calculate the dust influencing factor (K), and one script is dedicated to calculating the sinking velocity of particle-free Trichodesmium colonies (v0). All Python scripts are available on GitHub (https://github.com/Zhanzhu1110/Trichobuoyancy.git) and can be processed using the "Codespaces" function on GitHub. The file 'K given values' is a specialized script designed to simulate the dust factor (K), assuming seawater and dust densities of 1028 kg/m3 and 2500 kg/m3, respectively, with a colony radius of 1 mm.

This dataset includes the NEMO 4.0.2 configuration used and analysed in the paper titled "Eddy-driven heterogeneity in sea ice during the ice-growth season". The output data is approximately 4TB for the 3 idealised configuration used in the manuscript, thus we opted to distribute the configuration. Note: The initial conditions for each simulation are compressed into the file `init_cond.zip` The configuration for one of the simulations is compressed in the file `config.zip` In order to reproduce all the runs, it's only required to change the initial conditions in the file namelist_cfg and namelist_ice_cfg. Further information and scripts to reproduce the result of the manuscript can be found at: https://github.com/josuemtzmo/Ice_formation

These supplementary teaching resources align to the open textbook, Fish, Fishing, and Conservation which is a 389-page, peer-reviewed publicly-available, openly-licensed textbook intended for undergraduate students who are exploring majors in Fish & Wildlife. It is also relevant to a general audience or for use in courses which explore social and ethical aspects of fish, fishing and conservation. The open textbook, Fish, Fishing, and Conservation, is freely available at https://doi.org/10.21061/fishandconservation. Supplementary teaching resources include a sample course syllabus, schedule, and a variety of assignments. Individuals who wish to share their materials relevant to teaching in this subject area are encouraged to join and share their openly-licensed resources via the Fish, Fishing, and Conservation instructor group in OER Commons. Are you reviewing or adopting Fish, Fishing, and Conservation for a course? Please help us understand your use by filling out this form. VIVA (Virtual Library of Virginia)

The creation, movement, and consumption of distinct biomolecules by marine organisms has far reaching implications regarding ecosystem material and energy flow and how we manage the marine environment. Lipids are ubiquitous, energy rich biomolecules that are essential for all life and are used for cell membrane structure, energy storage and serve as useful indicators for ecosystem and food web dynamics. In this dissertation, the flow of specific lipid biomolecules through multiple marine environments is measured, explored, and clarified to better understand biogeochemical cycles, marine food webs and ecosystem connectivity. In the first chapter of my dissertation, I measure, quantify, and close the loop of the open ocean microbial hydrocarbon cycle, with implications for priming effects of the ocean microbiome to oil spills. It is estimated that seeps, spills, and other oil pollution introduce ~ 1.3 million tons (1.3 Tg) of hydrocarbons into the ocean each year. Additionally, it is known that globally abundant marine cyanobacteria Prochlorococcus and Synechococcus which account for ~25% of ocean net primary production also produce hydrocarbons from fatty acids. But little is known about the size, turnover and fate of these cyanobacterial hydrocarbons and the implications for the ocean’s microbiome response to future oil spills. From a research expedition in the North Atlantic, I report that cyanobacteria in an oligotrophic gyre mainly produce n-pentadecane which correlates tightly with fluorescence and Prochlorococcus abundance in oligotrophic waters. Using chemical and isotopic tracing I find that pentadecane production and diel dynamics mainly occurs in the lower euphotic zone at the deep chlorophyll maximum. I estimate the global flux of cyanobacteria-produced pentadecane exceeds total oil input in the ocean by 100 to 500-fold, with cyanobacteria producing ~ 130-650 million tons of pentadecane per year. Analysis of sinking particles at the base of the euphotic zone show that nearly all pentadecane (< 0.001 % remaining) is consumed within the euphotic zone, suggesting near complete consumption of these hydrocarbons by hydrocarbon degrading microbes. These findings characterize a wide-spread microbial hydrocarbon cycle that selectively primes the ocean’s microbiome with long-chain alkanes. In the second chapter of my dissertation, I conduct a large-scale feeding experiment on a symbiotic reef-building coral (Stylophora pistillata) in the Red Sea to clarify fatty acid and isotopic biomarker patterns of coral heterotrophy for use in the field. Coral heterotrophy is an often-overlooked facet of coral nutrition that provides essential nutrients that help corals resist and recover from thermally induced bleaching that is degrading reef ecosystems around the world due to rising global ocean temperatures. Yet, methods for measuring coral mixotrophy, the balance between organic matter contributions to the coral host from autotrophic photo endosymbionts and heterotrophy on particles and plankton have typically been too coarse to elucidate source contributions. Through my experiment I show that fatty acids and isotopic biomarkers reliably separate experimental and reef nutritional source groups (heterotrophic or autotrophic). I show that heterotrophic fatty acid biomarkers are reliably recorded into coral host and symbiont tissues, with a divergent metabolic pattern of autotrophic biomarkers as feeding increases due to positive feedback of heterotrophy on the in hospite photo symbiont population. Additionally, I show that nitrogen and essential fatty acids are preferentially recorded into coral tissue while most heterotrophic carbon is respired or exuded as mucous; this shows that the use of bulk carbon isotopes as a feeding proxy for the last ~ 40 years is largely underestimating the contribution of heterotrophy to the trophic ecology of reef building corals. Overall, this finding underscores a connectivity between oceanic phyto- and zooplankton and reef-building coral. In the third chapter of my dissertation, I explore the mixotrophic differences of divergent bleaching responses of Acropora hyacinthus colonies on the forereef of Mo’orea during the 2019 mass bleaching event. During this bleaching event, all colonies of A. hyacinthus on the deep forereef (14 m) bleached and recovered, while colonies on the shallow forereef (5 m) near the reef crest resisted bleaching entirely, despite the same temperature stress. Using fatty acid and isotopic biomarkers I show through several lines of evidence that bleaching resistant colonies near the reef crest were likely consuming more particulate organic matter than deep forereef colonies. This conclusion is supported by isotopic feeding proxies, less isotopic niche overlap of the host and symbiont of resistant colonies, and larger proportions of putative POM fatty acid biomarkers in the host of resistant colonies relative to recovered colonies. This interpretation is in line with observations that benthic communities on the reef crest are a net sink of oceanic POM and that increased reliance on heterotrophy is associated with bleaching resistance. These data show the vital importance of reef environment, coral heterotrophy, and planktonic subsidies in structuring bleaching response of corals in a warming ocean and ultimately show that the reef crest may serve as a potent zone for reseeding coral populations after marine heat waves.

Understanding what factors shape the magnitude of divergence under rapid evolution is critical. Phenotypic divergence, specifically, can be influenced by selective forces such as the environment (climate, geographic distance) as well as non-selective forces (genetic composition of the founding population). Threespine sticklebacks provide a unique opportunity to study the magnitude of divergence under rapid evolution. Marine sticklebacks independently colonized freshwater habitats at the end of the last ice age (~12,000 years ago) generating multiple replicate pairs that represent a natural experiment. However, studies rely on untested assumptions that marine sticklebacks are not phenotypically varied and are unchanged from their ancestors. Here, we test how differential environmental conditions impact the estimated magnitude of phenotypic divergence and parallelism of independent freshwater stickleback populations. We find that marine variation is comparable to freshwater variation. Importantly, the inferred magnitude of phenotypic divergence of each freshwater population is dependent on marine sampling location. The geographic distance and environmental similarity between the marine and freshwater pairs explain a significant degree of variance. When estimating the degree of parallelism among freshwater pairs, marine reference also affects the inferred magnitude. The observed pattern suggests the choice of reference population and its geographic distance are important aspects to consider when estimating freshwater divergence and parallelism. Results also implicate a signature of local adaptation and/or isolation by distance. We provide recommendations for choosing ecologically relevant marine references in future studies on this important evolutionary model system.

Widespread overuse and large-scale production of antibiotics create antibiotic pollution, disrupting environmental microbiota and creating a public health risk. Highly urbanized coastal environments can be under high impact from antibiotic pollution from many trails of polluted effluents and runoff. The city of Long Beach is one such coastal area under high impact, since it is highly urban, industrialized, and experiences frequent sewage spills. We collected water samples from the LA River in a transect running southwest into the San Pedro Channel in order to investigate (1) how does strength of antibiotic resistance change as distance from shore increases, and (2) does antibiotic resistance correlate with composition of the bacterial community. There was no consistent relationship between strength of antibiotic resistance and distance from shore. Instead, we found that bacteria from the Pacific Ocean showed higher antibiotic resistance than bacteria from the LA River in five out of eleven antibiotic treatments. We also found that the alpha diversity of bacterial communities was lower in the LA River samples compared, and alpha diversity positively correlated with strength of antibiotic resistance in four antibiotic treatments. Our findings highlight how prevalence of antibiotic pollution does not always follow a distance dilution, as well as the need for understanding the strength behind antibiotic resistance in marine bacteria.