<?xml version="1.0" encoding="UTF-8"?><resource xsi:schemaLocation="http://datacite.org/schema/kernel-4 http://schema.datacite.org/meta/kernel-4.3/metadata.xsd" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns="http://datacite.org/schema/kernel-4"><identifier identifierType="DOI">10.1594/PANGAEA.995157</identifier><creators><creator><creatorName>Bienhold, Christina</creatorName><givenName>Christina</givenName><familyName>Bienhold</familyName><nameIdentifier schemeURI="http://orcid.org/" nameIdentifierScheme="ORCID">0000-0003-2269-9468</nameIdentifier><affiliation affiliationIdentifierScheme="ROR" affiliationIdentifier="https://ror.org/032e6b942">Alfred Wegener Institute, Helmholtz Centre for Polar and Marine Research, Bremerhaven</affiliation><affiliation affiliationIdentifierScheme="ROR" affiliationIdentifier="https://ror.org/02385fa51">Max-Planck-Institut für Marine Mikrobiologie</affiliation></creator><creator><creatorName>Kohlenbach, Katharina</creatorName><givenName>Katharina</givenName><familyName>Kohlenbach</familyName></creator></creators><titles><title>Benthic prokaryotic cell densities from Polarstern expedition PS138 to the Central Arctic Ocean during August-September 2023</title></titles><publisher>PANGAEA</publisher><publicationYear>2026</publicationYear><subjects><subject>Central Arctic Ocean</subject><subject>Deep sea</subject><subject>Eurasian Basin</subject><subject>sediment biogeochemistry</subject><subject subjectScheme="Parameter">Event label</subject><subject subjectScheme="Parameter">Latitude of event</subject><subject subjectScheme="Parameter">Longitude of event</subject><subject subjectScheme="Parameter">Date/Time of event</subject><subject subjectScheme="Parameter">Elevation of event</subject><subject subjectScheme="Parameter">Sample ID</subject><subject subjectScheme="Parameter">Replicate, biological</subject><subject subjectScheme="Parameter">Replicate, technical</subject><subject subjectScheme="Parameter">Depth, sediment/rock, top/minimum</subject><subject subjectScheme="Parameter">Depth, sediment/rock, bottom/maximum</subject><subject subjectScheme="Parameter">Prokaryotes, abundance as single cells</subject><subject subjectScheme="Parameter">Comment</subject><subject subjectScheme="Method">Multicorer with television</subject><subject subjectScheme="Method">Acridine Orange Direct Counting (AODC)</subject><subject subjectScheme="Campaign">PS138</subject><subject subjectScheme="Basis">Polarstern</subject></subjects><dates><date dateType="Collected">2023-08-09T18:21:23/2023-09-18T23:05:43</date></dates><resourceType resourceTypeGeneral="Dataset">Dataset</resourceType><relatedIdentifiers><relatedIdentifier relatedIdentifierType="DOI" relationType="References">10.57738/BzPM_0788_2024</relatedIdentifier><relatedIdentifier relatedIdentifierType="DOI" relationType="References">10.1016/S0967-0637(97)00052-6</relatedIdentifier><relatedIdentifier relatedIdentifierType="DOI" relationType="References">10.3389/fmicb.2017.00266</relatedIdentifier><relatedIdentifier relatedIdentifierType="DOI" relationType="References">10.1007/BF00395813</relatedIdentifier></relatedIdentifiers><sizes><size>770 data points</size></sizes><formats><format>text/tab-separated-values</format></formats><rightsList><rights rightsURI="https://creativecommons.org/licenses/by/4.0/" schemeURI="https://spdx.org/licenses/" rightsIdentifierScheme="SPDX" rightsIdentifier="CC-BY-4.0">Creative Commons Attribution 4.0 International</rights><rights>Data access is restricted (moratorium, sensitive data, license constraints)</rights></rightsList><descriptions><description descriptionType="Abstract">Undisturbed sediment samples were obtained with a TV-guided multiple corer (TV-MUC). Upon retrieval of the MUC, the overlying water was carefully removed from each core and the upper few centimeters of sediment were cut using a steel plate and a custom-made plastic ring into the following depth horizons: 0-1 cm, 1-5 cm, 5-10 cm. For the determination of prokaryotic cell abundances, 2 ml sediment were ﬁxed in 9 ml formaldehyde/seawater at a ﬁnal concentration of 2-4% formaldehyde and stored at 4°C. Benthic prokaryotic cell abundances were determined using the Acridine Orange Direct Count (AODC) method (Meyer-Reil, 1983, doi:10.1007/BF00395813) following the protocol described in (Boetius and Damm, 1998, doi:10.1016/S0967-0637(97)00052-6; Hoffmann et al., 2017, doi:10.3389/fmicb.2017.00266). For 0-1 cm: 3 biological replicates, and 2 technical replicate filters per sample were counted. A total of 50 grids or at least 500 cells were counted per filter. For 1-5 cm: 2 biological replicates, and 2 technical replicate filters per sample were counted. A total of 50 grids or at least 250 cells were counted per filter.For 5-10 cm: 1 biological replicate, and 2 technical replicate filters per sample were counted. A total of 50 grids or at least 100 cells were counted per filter. Because cell numbers were so low in the deeper sediment layers, these numbers need to be treated with caution.</description></descriptions><geoLocations><geoLocation><geoLocationBox><westBoundLongitude>31.548253</westBoundLongitude><eastBoundLongitude>130.170545</eastBoundLongitude><southBoundLatitude>82.908155</southBoundLatitude><northBoundLatitude>89.945032</northBoundLatitude></geoLocationBox></geoLocation></geoLocations></resource>