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            <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/dataset/932236.rdf" xlink:actuate="onRequest">ZooSCAN images of zooplankton collected with MOCNESS tows during six R/V Atlantic Explorer cruises in the northwest Atlantic (Sargasso Sea) from 2021 to 2023</gmx:Anchor>
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                <gmx:Anchor xlink:href="http://orcid.org/0000-0002-3730-2876" xlink:title="ORCID" xlink:actuate="onRequest">Amy Elizabeth Maas</gmx:Anchor>
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            <gco:CharacterString>Cite this dataset as: Maas, A., Blanco-Bercial, L. (2024) ZooSCAN images of zooplankton collected with MOCNESS tows during six R/V Atlantic Explorer cruises in the northwest Atlantic (Sargasso Sea) from 2021 to 2023. Biological and Chemical Oceanography Data Management Office (BCO-DMO). (Version 1) Version Date 2024-07-11 [if applicable, indicate subset used]. doi:10.26008/1912/bco-dmo.932236.1 [access date]</gco:CharacterString>
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        <gco:CharacterString>Methods and Sampling: &amp;lt;p&amp;gt;One pair of 1m&amp;lt;sup&amp;gt;2&amp;lt;/sup&amp;gt; MOCNESS (Multiple Open Closing Nets with Environmental Sensor System) tows were performed during each cruise- one during the day, and one at night (MOCNESS, Wiebe et al, 1985). Nets with 150um mesh were used to better capture the smaller midwater zooplankton community in the region. Eight nets were fired in sequence along the upcast to capture spatially discrete zooplankton samples between 600m and the surface. While nets one, two, and three consistently targeted depths of 600-500m, 500m-400m, and 400-300m, depths for nets four through eight varied based on hydrographic features including the thermocline, deep chlorophyll maximum, and oxygen minimum zone (Maas et al, 2014, Steinberg et al, 2008).&amp;amp;nbsp; Once onboard, samples were split in two using a Motoda splitter (Motoda, 1959)&amp;amp;nbsp; with half preserved with sodium tetraborate buffered 4% formalin in seawater to be scanned with a ZooSCAN&amp;amp;nbsp;(Gorsky et al, 2010) and half placed in 95% undenatured ethanol for metabarcoding.&amp;amp;nbsp;&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;A representative subsample of the formalin-preserved zooplankton community from each net were imaged using a ZooSCAN ver. 4 at either 4,800 dpi or 2,400 dpi (following the methods in: Gorsky et al., 2010, Vandromme et al., 2012 as detailed in Maas et al. 2021). The change in resolution partway through the project was a result of recommendations from Hydroptic and loss of software support for 4800dpi imaging. In order to better represent all size classes in the images, the original sample was divided into three size categories. All individuals larger than 2 cm were selected by eye and scanned separately from all the others (fraction &amp;quot;d1&amp;quot;). The remainder of the sample was sieved through a 1-mm mesh sieve, and both size fractions were individually scanned (&amp;quot;d2&amp;quot; &amp;amp;gt;1000um, &amp;quot;d3&amp;quot; 153-1000um). From these smaller size fractions, at least 1500 particles were scanned after subsampling using a Motoda splitter (Motoda, 1959), requiring generation of two separate scans for both size classes. This resulted in a total of five images per net.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;&amp;lt;strong&amp;gt;Image names:&amp;lt;/strong&amp;gt;&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Image names include:&amp;lt;br /&amp;gt;
cruise#_mocnessID_net#_sizefraction_ and _a|b if a replicate and end in _raw_1.tif&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Multiple images of the same size fraction were sometimes taken to obtain a sufficient number of particles. These replicates are named a or b. If there is no replicate they don’t have a letter in the image name. An a and b scan were always done for size classes d2 and d3.&amp;amp;nbsp; This was important because the split size is for the sum of a+b (e.g. if a is ¼ and b is ¼, the acq_sub_part will be 0.5).&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;&amp;lt;strong&amp;gt;Example of image names:&amp;lt;/strong&amp;gt;&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;ae2112_m22_n4_d3_a_raw_1.tif&amp;amp;nbsp; [a replicate]&amp;lt;br /&amp;gt;
ae2112_m22_n4_d3_b_raw_1.tif&amp;amp;nbsp;&amp;amp;nbsp;[b replicate]&amp;lt;br /&amp;gt;
ae2204_m27_n5_d1_raw_1.tif&amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp;&amp;amp;nbsp;[no&amp;amp;nbsp;replicate]&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Related Datasets may contain the &amp;quot;object_id&amp;quot; (the particle/organism id) which is constructed the same way as the image name except it as an additional _#&amp;amp;nbsp;at the end.&amp;amp;nbsp; This additional number in the object_id is added by the ZooProcess software (Hydroptic, 2016).&amp;lt;br /&amp;gt;
e.g.&amp;lt;br /&amp;gt;
object_id:&amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp;ae1614_m3_n1_d2_a_1_100&amp;lt;br /&amp;gt;
image_name: ae1614_m3_n1_d2_a_1.tif&amp;lt;/p&amp;gt;</gco:CharacterString>
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        <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/award/835244.rdf" xlink:title="OCE-2023621" xlink:actuate="onRequest">Funding provided by NSF Division of Ocean Sciences (NSF OCE) Award Number: OCE-2023621 Award URL: https://www.nsf.gov/awardsearch/show-award?AWD_ID=2023621</gmx:Anchor>
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        <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/award/835246.rdf" xlink:title="OCE-2023372" xlink:actuate="onRequest">Funding provided by NSF Division of Ocean Sciences (NSF OCE) Award Number: OCE-2023372 Award URL: https://www.nsf.gov/awardsearch/show-award?AWD_ID=2023372</gmx:Anchor>
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                <gco:CharacterString>&amp;lt;p&amp;gt;One pair of 1m&amp;lt;sup&amp;gt;2&amp;lt;/sup&amp;gt; MOCNESS (Multiple Open Closing Nets with Environmental Sensor System) tows were performed during each cruise- one during the day, and one at night (MOCNESS, Wiebe et al, 1985). Nets with 150um mesh were used to better capture the smaller midwater zooplankton community in the region. Eight nets were fired in sequence along the upcast to capture spatially discrete zooplankton samples between 600m and the surface. While nets one, two, and three consistently targeted depths of 600-500m, 500m-400m, and 400-300m, depths for nets four through eight varied based on hydrographic features including the thermocline, deep chlorophyll maximum, and oxygen minimum zone (Maas et al, 2014, Steinberg et al, 2008).&amp;amp;nbsp; Once onboard, samples were split in two using a Motoda splitter (Motoda, 1959)&amp;amp;nbsp; with half preserved with sodium tetraborate buffered 4% formalin in seawater to be scanned with a ZooSCAN&amp;amp;nbsp;(Gorsky et al, 2010) and half placed in 95% undenatured ethanol for metabarcoding.&amp;amp;nbsp;&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;A representative subsample of the formalin-preserved zooplankton community from each net were imaged using a ZooSCAN ver. 4 at either 4,800 dpi or 2,400 dpi (following the methods in: Gorsky et al., 2010, Vandromme et al., 2012 as detailed in Maas et al. 2021). The change in resolution partway through the project was a result of recommendations from Hydroptic and loss of software support for 4800dpi imaging. In order to better represent all size classes in the images, the original sample was divided into three size categories. All individuals larger than 2 cm were selected by eye and scanned separately from all the others (fraction &amp;quot;d1&amp;quot;). The remainder of the sample was sieved through a 1-mm mesh sieve, and both size fractions were individually scanned (&amp;quot;d2&amp;quot; &amp;amp;gt;1000um, &amp;quot;d3&amp;quot; 153-1000um). From these smaller size fractions, at least 1500 particles were scanned after subsampling using a Motoda splitter (Motoda, 1959), requiring generation of two separate scans for both size classes. This resulted in a total of five images per net.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;&amp;lt;strong&amp;gt;Image names:&amp;lt;/strong&amp;gt;&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Image names include:&amp;lt;br /&amp;gt;
cruise#_mocnessID_net#_sizefraction_ and _a|b if a replicate and end in _raw_1.tif&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Multiple images of the same size fraction were sometimes taken to obtain a sufficient number of particles. These replicates are named a or b. If there is no replicate they don’t have a letter in the image name. An a and b scan were always done for size classes d2 and d3.&amp;amp;nbsp; This was important because the split size is for the sum of a+b (e.g. if a is ¼ and b is ¼, the acq_sub_part will be 0.5).&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;&amp;lt;strong&amp;gt;Example of image names:&amp;lt;/strong&amp;gt;&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;ae2112_m22_n4_d3_a_raw_1.tif&amp;amp;nbsp; [a replicate]&amp;lt;br /&amp;gt;
ae2112_m22_n4_d3_b_raw_1.tif&amp;amp;nbsp;&amp;amp;nbsp;[b replicate]&amp;lt;br /&amp;gt;
ae2204_m27_n5_d1_raw_1.tif&amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp;&amp;amp;nbsp;[no&amp;amp;nbsp;replicate]&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Related Datasets may contain the &amp;quot;object_id&amp;quot; (the particle/organism id) which is constructed the same way as the image name except it as an additional _#&amp;amp;nbsp;at the end.&amp;amp;nbsp; This additional number in the object_id is added by the ZooProcess software (Hydroptic, 2016).&amp;lt;br /&amp;gt;
e.g.&amp;lt;br /&amp;gt;
object_id:&amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp;ae1614_m3_n1_d2_a_1_100&amp;lt;br /&amp;gt;
image_name: ae1614_m3_n1_d2_a_1.tif&amp;lt;/p&amp;gt;</gco:CharacterString>
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                <gco:CharacterString>&amp;lt;p&amp;gt;Scans were processed using&amp;amp;nbsp;ZooProcess&amp;amp;nbsp;(version 8.22, ImageJ macro suite). The &amp;quot;Convert and process from RAW&amp;quot; function was used to separate particles into individual vignettes and generate a suite of measurements for each particle. &amp;quot;Doubles&amp;quot; (vignettes containing more than one particle) were manually separated in the software and reprocessed.&amp;amp;nbsp;&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Processed scans and their corresponding metadata were then uploaded to Ecotaxa (Picheral et al,&amp;amp;nbsp;https://ecotaxa.obs-vlfr.fr/), where a training set was created using manually classified images from this project as well as existing validated images from other projects in the Sargasso Sea. Classification categories were chosen based on taxon of interest, identification level in previous projects, and known limitations of the software. Generally, broader level taxonomic groups are used. Identification of all particles was predicted, then manually validated.&amp;amp;nbsp;&amp;lt;/p&amp;gt;</gco:CharacterString>
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        <gmd:processStep xlink:title="BCO-DMO Data Processing Description">
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                <gmd:description>
                  <gco:CharacterString>Version 1: 
* All raw scan images were bundled into zip files named by &amp;lt;cruise_id&amp;gt;_&amp;lt;mocness_id&amp;gt;.zip
* The filesize and md5 checksum was added to the image metadata table.
**  After images were transferred to BCO-DMO, a file inventory was made containing the filename, filesize in bytes, and checksum (md5sum).  This file inventory table was joined with the provided metadata table to verify the file collection is complete without any missing files.
* an additional supplemental file was added containing metadata for each file (including zips) which includes file access links to aid in programmatic download of all image bundles in the dataset once the dataset is released.
* two imagenames in the metadata table were changed to match the actual filenames. The data submitter was consulted and advised this was the correct course of action. The 3 was omitted in d3 of the imagename.
image_name ae2124_m24_n1_d_a_raw_1.tif -&amp;gt; ae2124_m24_n1_d3_a_raw_1.tif
image_name ae2124_m24_n1_d_b_raw_1.tif -&amp;gt; ae2124_m24_n1_d3_b_raw_1.tif</gco:CharacterString>
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                          <gco:CharacterString>Specified by BCO-DMO Data Managers</gco:CharacterString>
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    <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/affiliation/191.rdf" xlink:actuate="onRequest">Biological and Chemical Oceanography Data Management Office (BCO-DMO)</gmx:Anchor>
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		  <gmd:hoursOfService>
        <gco:CharacterString>Monday - Friday 8:00am - 5:00pm</gco:CharacterString>
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		  <gmd:contactInstructions>
		    <gco:CharacterString>For questions regarding this resource, please contact BCO-DMO via the email address provided.</gco:CharacterString>
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                <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/instrument/437.rdf" xlink:title="MOCNESS1" xlink:actuate="onRequest">MOCNESS (1m2 mouth size)</gmx:Anchor>
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            <gco:CharacterString>PI Supplied Instrument Name: MOCNESS (1m2 mouth size) PI Supplied Instrument Description:The Multiple Opening/Closing Net and Environmental Sensing System or MOCNESS is a family of net systems based on the Tucker Trawl principle. There are currently 8 different sizes of MOCNESS in existence which are designed for capture of different size ranges of zooplankton and micro-nekton. Each system is designated according to the size of the net mouth opening and in two cases, the number of nets it carries. The original MOCNESS (Wiebe et al, 1976) was a redesigned and improved version of a system described by Frost and McCrone (1974)(from MOCNESS manual). The MOCNESS used in this experiment is a 1m2 (mouth size) rigged with nine 150um mesh nets. One is flown open on the downcast to balance the net (Net 0- contents preserved but not analyzed), and the other eight (Net 1-8) are triggered on the upcast at desired depths. This particular MOCNESS was originally manufactured by Biological Environmental Sensor Systems (BESS), but was refit with new electronics from SIO/STS in 2017 (Net Interface Unit, Net Angle Sensor) to allow it to interface with Seabird instruments (SBE9Plus CTD, SBE3S Temperature, SBE4C Conductivity, SBE11 Deck Box).  Instrument Name: MOCNESS1 Instrument Short Name:MOC1   Instrument Description: The Multiple Opening/Closing Net and Environmental Sensing System or MOCNESS is a family of net systems based on the Tucker Trawl principle. The MOCNESS-1 carries nine 1-m2 nets usually of 335 micrometer mesh and is intended for use with the macrozooplankton.  All nets are black to reduce contrast with the background.  A motor/toggle release assembly is mounted on the top portion of the frame and stainless steel cables with swaged fittings are used to attach the net bar to the toggle release.  A stepping motor in a pressure compensated case filled with oil turns the escapement crankshaft of the toggle release which sequentially releases the nets to an open then closed position on command from the surface. -- from the MOCNESS Operations Manual (1999 + 2003). Community Standard Description: http://vocab.nerc.ac.uk/collection/L22/current/NETT0097/</gco:CharacterString>
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                <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/instrument/854072.rdf" xlink:title="ZooSCAN" xlink:actuate="onRequest">ZooSCAN ver. 4</gmx:Anchor>
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            <gco:CharacterString>PI Supplied Instrument Name: ZooSCAN ver. 4 PI Supplied Instrument Description:A representative subsample of the formalin-preserved zooplankton community from each net were imaged using a ZooSCAN ver. 4 at either 4,800 dpi or 2,400 dpi (following the methods in: Gorsky et al., 2010, Vandromme et al., 2012 as detailed in Maas et al. 2021). Instrument Name: ZooSCAN Instrument Short Name:   Instrument Description: Description excerpt from Hydroptic website
http://www.hydroptic.com/index.php/public/Page/product_item/ZOOSCAN

The ZooSCAN (CNRS patent) system makes use of scanner technology with custom lighting and a watertight scanning chamber into which liquid zooplankton samples can be placed. The scanner recovers a high-resolution, digitial image and the sample can be recovered without damage.  These digital images can then be investigated by computer processing. While the resolution of the digitized zooplankton images is lower than the image obtained using a binocular microscope this technique has proved to be more than adequate for large sample sets. Identification of species is done by automatic comparison of the image (vignette) of each individual animal in the scanned image with a library data set which may be built by the investigator for each individual survey or imported from a previous survey. The latest machine learning algorithm allows high recognition levels even if we recommend complementary manual sorting to achieve a high number of taxonomic groups.</gco:CharacterString>
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                  <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/deployment/931891.rdf" xlink:title="Cruise" xlink:actuate="onRequest">AE2112</gmx:Anchor>
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