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                    <gco:CharacterString>INSPIRE Implementing rules laying down technical arrangements for the interoperability and harmonisation of unknown theme</gco:CharacterString>
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                  <gmd:date>
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                      <gmd:date>
                        <gco:Date>2011</gco:Date>
                      </gmd:date>
                      <gmd:dateType>
                        <gmd:CI_DateTypeCode codeList="https://schemas.isotc211.org/schemas/19139/resources/codelist/gmxCodelists.xml#CI_DateTypeCode" codeListValue="publication">publication</gmd:CI_DateTypeCode>
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              <gmd:explanation>
                <gco:CharacterString>See the referenced specification</gco:CharacterString>
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              <gmd:pass>
                <gco:Boolean>false</gco:Boolean>
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        </gmd:DQ_DomainConsistency>
      </gmd:report>
      <gmd:lineage>
        <gmd:LI_Lineage>
          <gmd:statement>
            <gco:CharacterString>Sample equipment types used included: Corer: Box. National Oceanography Centre was contracted to undertake the survey on behalf of Natural Environment Research Council. Sediment samples were collected from megacores (max 60 cm), ROV pushcores (max 30 cm, with one XL pushcore of 60 cm) and 5 metre gravity core. The megacores and gravity cores were wireline deployed over the side of the James Cook. Extensive ROV video footage and imaging allowed groundtruthing and precise landing location cataloguing for many megacores and gravity cores. ROV push cores were taken by ROV pilots in locations specified by scientists onboard, also allowing for precise location information. Once retrieved on deck, gravity cores were sectioned into roughly one metre sections labelled from (surface) A, B, C, D, E (base). Cylindrical sediment samples were collected using cut off syringes and porewater extracted using rhizomes (and split into aliquots for different analyses). Megacores and pushcore sediment was sampled by extrusion and slicing at set intervals. Sampling was generally 1 cm slices in the top 10 cm and 2 cm thick slices below 10 cm. Porewater was extracted at similar intervals using rhizomes and split into aliquots for different analyses. During deployment of boxcores, nodules were collected. After these nodules had been checked for fauna/biota by the biologists, they were washed to reduce salt build up, set out to dry, photographed in trays and bagged up in bulk bags by station number. They were then sealed. Nodules were also measured in three dimensions and data recorded.</gco:CharacterString>
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