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            <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/dataset/881801.rdf" xlink:actuate="onRequest">Faunal ID, size and biomass on oyster reefs in Quonochontaug Pond, RI from July-August 2018 and September-October 2018</gmx:Anchor>
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            <gco:CharacterString>Cite this dataset as: Hughes, A. R., Davenport, T., Grabowski, J. (2022) Faunal ID, size and biomass on oyster reefs in Quonochontaug Pond, RI from July-August 2018 and September-October 2018. Biological and Chemical Oceanography Data Management Office (BCO-DMO). (Version 1) Version Date 2022-11-02 [if applicable, indicate subset used]. doi:10.26008/1912/bco-dmo.881801.1 [access date]</gco:CharacterString>
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        <gco:CharacterString>Fauna on restored oyster reefs Dataset Description:  Methods and Sampling: &amp;lt;p&amp;gt;These data were published in Davenport et al., 2022 (Restoration Ecology). All figure numbers mentioned refer to Davenport et al., 2022 (Restoration Ecology).&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;To compare reef-associated community colonization among oyster reef and sand habitats, we deployed experimental sampling trays assigned to four treatments in Quonochontaug Pond, Rhode Island, USA (41.3 N, 71.7 W). Sampling trays (plastic bakery trays, 0.66 meters L x 0.56 meters W x 0.14 meters H) were lined with fiberglass window screen (1-millimeter mesh opening). For the reef edge, reef interior, and shell treatments, trays were filled with five gallons of clean, articulated oyster shell from a shell recycling program run by The Nature Conservancy. For the sand treatment, the sampling trays were lined as before but filled with ten gallons of locally-sourced sand that was sieved to remove live organisms. Reef edge treatments of a single tray filled with shell were placed abutting each reef at a position randomized by cardinal direction (Fig. S3). Reef interior treatments of a single tray filled with shell were placed at the innermost point on each reef (Fig. S3). Shell and sand treatments of a single tray filled with shell or sand, respectively, were placed in each control plot (Fig. S3). Trays were deployed by divers on SCUBA on July 10, 2018 (summer) and September 7, 2018 (fall) and were leveled with surrounding substrate by carefully excavating the surrounding reef material (interior treatment) or sediment (edge, shell, and sand treatments).&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;After 28-29 days, divers collected the trays by carefully lifting them off the substrate and noting any organisms that escaped during retrieval. Divers brought the trays to the boat where fish were removed and euthanized in a eugenol/seawater solution before they were bagged and all tray contents placed in coolers. Tray contents were rinsed, sieved and sorted and all individuals were removed and stored in 10% isopropyl alcohol. Individuals were enumerated and identified to the lowest possible taxonomic group, measured, and weighed (wet weight in grams). Trays were rinsed and allowed to dry fully between deployments. Two trays were upturned during the fall deployment (block 1 reef interior; block 3 reef interior), leading to 24 trays sampled in summer and 22 trays in fall.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Measurements are total length to the nearest 1 millimeter (mm) for fishes, carapace width to nearest 0.1 mm for crabs, carapace length to nearest 0.1 mm for shrimps, shell height to nearest 0.1 mm for snails, and shell length to the nearest 0.1 mm for slipper shells. Fish measurements were determined with a metric ruler. All other organisms were measured with Vernier calipers. For species found at high densities, a subset (up to 20 individuals per species per sample) was weighed individually, after which organisms were weighed in bulk by species. Polychaetes were not measured, were weighed in bulk, and were only counted if heads were present.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Tray contents were rinsed with fresh water over a 1-mm sieve and stored in 10% isopropyl alcohol for approximately 1-6 months prior to identification and size and biomass measurements.&amp;lt;/p&amp;gt;</gco:CharacterString>
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        <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/award/709941.rdf" xlink:title="OCE-1652320" xlink:actuate="onRequest">Funding provided by NSF Division of Ocean Sciences (NSF OCE) Award Number: OCE-1652320 Award URL: https://www.nsf.gov/awardsearch/show-award?AWD_ID=1652320</gmx:Anchor>
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	Name: tray
	Units: unitless
	Description: &lt;p&gt;unique indicator for each experimental sampling tray.&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/881824.rdf
	Name: block
	Units: unitless
	Description: &lt;p&gt;numerical label for experimental block, 1-3; corresponds to Figure 1 in Davenport et al. 2022, Restoration Ecology.&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/881825.rdf
	Name: reef
	Units: unitless
	Description: &lt;p&gt;alphabetical label for the reef on which trays with HOBO loggers were attached; corresponds to Figure 1 in Davenport et al. 2022. Restoration Ecology&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/881826.rdf
	Name: treat
	Units: unitless
	Description: &lt;p&gt;experimental treatment, including I (reef interior), E (reef edge), SHELL (shell control tray). Corresponds to Figure 1 in Davenport et al. 2022, Restoration Ecology.&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/881827.rdf
	Name: species
	Units: unitless
	Description: &lt;p&gt;scientific name including genus and species where known otherwise the lowest taxonomic group is listed with spp. 1 indicating individuals of the same group. A taxon followed by biomass (e.g. &amp;quot;taxon - biomass&amp;quot;) indicates the specimen could not be identified to species since it was too damaged but the specimen was added to the biomass for its taxon. Where common name replaces a scientific name (e.g. &amp;quot;Ribbon worm&amp;quot;)  this individual was not identified to species&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/881828.rdf
	Name: meas_descrip
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http://lod.bco-dmo.org/id/dataset-parameter/881829.rdf
	Name: meas
	Units: millimeters (mm)
	Description: &lt;p&gt;measurement of organism size. Organisms for which measurements would be unreliable (e.g. crabs with broken shells) were not measured.&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/881830.rdf
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http://lod.bco-dmo.org/id/dataset-parameter/881831.rdf
	Name: wet_weight
	Units: grams (g)
	Description: &lt;p&gt;wet weight in grams. Organisms were blotted three times with lint-free wipes before weighing.&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/881832.rdf
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	Description: &lt;p&gt;year of tray deployment in format: YYYY&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/881833.rdf
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&amp;lt;p&amp;gt;To compare reef-associated community colonization among oyster reef and sand habitats, we deployed experimental sampling trays assigned to four treatments in Quonochontaug Pond, Rhode Island, USA (41.3 N, 71.7 W). Sampling trays (plastic bakery trays, 0.66 meters L x 0.56 meters W x 0.14 meters H) were lined with fiberglass window screen (1-millimeter mesh opening). For the reef edge, reef interior, and shell treatments, trays were filled with five gallons of clean, articulated oyster shell from a shell recycling program run by The Nature Conservancy. For the sand treatment, the sampling trays were lined as before but filled with ten gallons of locally-sourced sand that was sieved to remove live organisms. Reef edge treatments of a single tray filled with shell were placed abutting each reef at a position randomized by cardinal direction (Fig. S3). Reef interior treatments of a single tray filled with shell were placed at the innermost point on each reef (Fig. S3). Shell and sand treatments of a single tray filled with shell or sand, respectively, were placed in each control plot (Fig. S3). Trays were deployed by divers on SCUBA on July 10, 2018 (summer) and September 7, 2018 (fall) and were leveled with surrounding substrate by carefully excavating the surrounding reef material (interior treatment) or sediment (edge, shell, and sand treatments).&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;After 28-29 days, divers collected the trays by carefully lifting them off the substrate and noting any organisms that escaped during retrieval. Divers brought the trays to the boat where fish were removed and euthanized in a eugenol/seawater solution before they were bagged and all tray contents placed in coolers. Tray contents were rinsed, sieved and sorted and all individuals were removed and stored in 10% isopropyl alcohol. Individuals were enumerated and identified to the lowest possible taxonomic group, measured, and weighed (wet weight in grams). Trays were rinsed and allowed to dry fully between deployments. Two trays were upturned during the fall deployment (block 1 reef interior; block 3 reef interior), leading to 24 trays sampled in summer and 22 trays in fall.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Measurements are total length to the nearest 1 millimeter (mm) for fishes, carapace width to nearest 0.1 mm for crabs, carapace length to nearest 0.1 mm for shrimps, shell height to nearest 0.1 mm for snails, and shell length to the nearest 0.1 mm for slipper shells. Fish measurements were determined with a metric ruler. All other organisms were measured with Vernier calipers. For species found at high densities, a subset (up to 20 individuals per species per sample) was weighed individually, after which organisms were weighed in bulk by species. Polychaetes were not measured, were weighed in bulk, and were only counted if heads were present.&amp;lt;/p&amp;gt;

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&amp;lt;p&amp;gt;&amp;lt;strong&amp;gt;BCO-DMO Processing:&amp;lt;/strong&amp;gt;&amp;lt;br /&amp;gt;
- Adjusted field/parameter names to comply with BCO-DMO naming conventions&amp;lt;br /&amp;gt;
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- Values in column &amp;quot;wet_weight&amp;quot; were rounded to 3 decimal places for all trays except t1&amp;lt;br /&amp;gt;
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