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        <gco:CharacterString>Sample data for Lottia genomic samples Dataset Description:  Methods and Sampling: &amp;lt;p&amp;gt;We sampled 19 sites on the Pacific coast of North America, spanning most of the contemporary range of&amp;amp;nbsp;&amp;lt;em&amp;gt;Lottia&amp;amp;nbsp;gigantea &amp;lt;/em&amp;gt;(urn:lsid:marinespecies.org:taxname:456593)&amp;lt;em&amp;gt;.&amp;amp;nbsp;&amp;lt;/em&amp;gt;We non-lethally excised a small piece of foot muscle tissue. For all locations except the four northern sites, we collected tissue from roughly 30 individuals per site, comprised of 10 individuals within each of the following size ranges: 10–25 mm (small), 30–40 mm (medium), and &amp;amp;gt;40 mm (large). Sampling of the four northern sites (i.e., expanded range) also consisted of roughly 10 small, medium, and large individuals per site. However, as individual limpets at these four sites have been closely monitored over the past 8 years, these sites had known cohorts based on the estimated year of settlement. Size classes at sites for which we do not have monitoring data were chosen based on our data and previous growth curves (Kido &amp;amp;amp; Murray,&amp;amp;nbsp;2003) to approximately group individuals into those that settled during the marine heatwaves (MHWs), soon after the MHWs (late 2016 or late 2017), or well after the MHWs (late 2018 or late 2019).&amp;amp;nbsp;Tissue was stored in 90% ethanol at −20°C. We used the Qiagen DNeasy extraction kit to perform DNA extractions following the manufacturer's protocols. DNA quantity and quality were assessed with NanoDrop, Qubit, and gel electrophoresis. Library preparation followed the Nextera Lite protocol, with adaptations following Rowan et&amp;amp;nbsp;al.&amp;amp;nbsp;(2019). Briefly, this consisted of normalizing samples, tagmentation, PCR, pooling samples, and bead size selection. The purified samples were run on a High Sensitivity DNA Bioanalyzer chip and then sent to BGI Genomics for whole-genome sequencing on the DNBSEQ-T7 PE150 platform on four lanes of sequencing.&amp;lt;/p&amp;gt;</gco:CharacterString>
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        <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/award/867542.rdf" xlink:title="OCE-2023297" xlink:actuate="onRequest">Funding provided by NSF Division of Ocean Sciences (NSF OCE) Award Number: OCE-2023297 Award URL: https://www.nsf.gov/awardsearch/show-award?AWD_ID=2023297</gmx:Anchor>
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Anthropogenic climate change is shifting the distributions of species across the globe. Such contemporary shifts in species’ ranges may have cascading effects on entire ecosystems. This project disentangles the mechanisms underlying climate-driven species range shifts in marine systems using the intertidal owl limpet as a case study. During the recent marine heatwaves off the Pacific coast of North America, populations at the northern range limit in northern California have expanded, with ongoing reproduction even after termination of the heatwave events. This is therefore an ideal system to explore the dynamics of natural selection that occur as species occupy new regions. Broadly, this project deepens understanding of how range shifts occur in marine systems and furthers the ability to predict future species distributions in response to climate change. The project provides research experiences for high school and undergraduate students from historically underrepresented groups by engaging with existing, demonstrably-effective programs. The investigators host leadership and skill-building workshops for senior female graduate students and engage the public in partnership with the California Academy of Sciences, Bodega Marine Lab, and San Francisco Exploratorium. Finally, the project provides training for a postdoctoral scholar and two graduate students.&lt;/p&gt;
&lt;p&gt;Although phenomenological studies suggest that climate-associated range shifts are common in marine systems, to date, mechanistic studies of the climate-organism interactions that alter geographic distributions have largely focused on terrestrial systems. However, dispersal dynamics greatly differ in many marine systems, as currents may frequently transport planktonic larvae into new environmental regimes. This project integrates detailed demographic observations of the recent range expansion of the intertidal owl limpet, Lottia gigantea, with ecological, phenotypic, and genomic measurements of divergence across its range. Specifically, the work 1) documents phenotypic divergence in larval and juvenile traits across the zone of range expansion, 2) uses whole genome sequencing to estimate gene flow across the entire range, 3) identifies genomic patterns of selection across the zone of range expansion and through time, and 4) identifies drivers of variation in performance over latitudinal and microgeographic scales. The ability to monitor this range shift in real time, along with the suitability of this system for tracking individuals across multiple years, allows the investigators to examine the impact of selection in novel range-edge conditions at the phenotypic and genomic levels, and scale from individuals to species-level responses to ongoing environmental change.&lt;/p&gt;
&lt;p&gt;This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the Foundation's intellectual merit and broader impacts review criteria.&lt;/p&gt;</gco:CharacterString>
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                <gco:CharacterString>&amp;lt;p&amp;gt;We sampled 19 sites on the Pacific coast of North America, spanning most of the contemporary range of&amp;amp;nbsp;&amp;lt;em&amp;gt;Lottia&amp;amp;nbsp;gigantea &amp;lt;/em&amp;gt;(urn:lsid:marinespecies.org:taxname:456593)&amp;lt;em&amp;gt;.&amp;amp;nbsp;&amp;lt;/em&amp;gt;We non-lethally excised a small piece of foot muscle tissue. For all locations except the four northern sites, we collected tissue from roughly 30 individuals per site, comprised of 10 individuals within each of the following size ranges: 10–25 mm (small), 30–40 mm (medium), and &amp;amp;gt;40 mm (large). Sampling of the four northern sites (i.e., expanded range) also consisted of roughly 10 small, medium, and large individuals per site. However, as individual limpets at these four sites have been closely monitored over the past 8 years, these sites had known cohorts based on the estimated year of settlement. Size classes at sites for which we do not have monitoring data were chosen based on our data and previous growth curves (Kido &amp;amp;amp; Murray,&amp;amp;nbsp;2003) to approximately group individuals into those that settled during the marine heatwaves (MHWs), soon after the MHWs (late 2016 or late 2017), or well after the MHWs (late 2018 or late 2019).&amp;amp;nbsp;Tissue was stored in 90% ethanol at −20°C. We used the Qiagen DNeasy extraction kit to perform DNA extractions following the manufacturer's protocols. DNA quantity and quality were assessed with NanoDrop, Qubit, and gel electrophoresis. Library preparation followed the Nextera Lite protocol, with adaptations following Rowan et&amp;amp;nbsp;al.&amp;amp;nbsp;(2019). Briefly, this consisted of normalizing samples, tagmentation, PCR, pooling samples, and bead size selection. The purified samples were run on a High Sensitivity DNA Bioanalyzer chip and then sent to BGI Genomics for whole-genome sequencing on the DNBSEQ-T7 PE150 platform on four lanes of sequencing.&amp;lt;/p&amp;gt;</gco:CharacterString>
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                  <gco:CharacterString>- Loaded Lottia_metadata.xlsx into BCO-DMO system
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- Renamed multiple fields: &amp;quot;Library Name&amp;quot; → Library_Name, &amp;quot;Sample ID&amp;quot; → Sample_ID, &amp;quot;% Dups&amp;quot; → Percent_Dups, &amp;quot;% GC&amp;quot; → Percent_GC, &amp;quot;Read_Length&amp;quot; → Average_read_length, &amp;quot;M Seqs&amp;quot; → M_Seqs, &amp;quot;#reads&amp;quot; → num_reads, &amp;quot;read_length&amp;quot; → sequencer_read_length , &amp;quot;read X read length&amp;quot; → read_X_read_length, &amp;quot;genome size&amp;quot; → genome_size
- Standardized site text in lottia_reads.cov-1 via find/replace to comply with BCO-DMO character guidance: “Bahía Asunción”→“Bahia Asuncion”; then “Bahía”→“Bahia”
- Renamed resource lottia_reads.cov-1 to 958640_v1_lottia_genome.
- Exported final output as CSV named 958640_v1_lottia_genome.csv

Accepted species identifier confirmed on 2026-03-17.</gco:CharacterString>
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                <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/instrument/649.rdf" xlink:title="Automated DNA Sequencer" xlink:actuate="onRequest">DNBSEQ-T7 PE150 platform</gmx:Anchor>
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The purified samples were run on a High Sensitivity DNA Bioanalyzer chip and then sent to BGI Genomics for whole-genome sequencing on the DNBSEQ-T7 PE150 platform on four lanes of sequencing. Instrument Name: Automated DNA Sequencer Instrument Short Name:Automated Sequencer   Instrument Description: A DNA sequencer is an instrument that determines the order of deoxynucleotides in deoxyribonucleic acid sequences.</gco:CharacterString>
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                <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/instrument/626182.rdf" xlink:title="Bioanalyzer" xlink:actuate="onRequest">High Sensitivity DNA Bioanalyzer chip</gmx:Anchor>
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                <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/instrument/484.rdf" xlink:title="Fluorometer" xlink:actuate="onRequest">Qubit</gmx:Anchor>
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                <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/instrument/867997.rdf" xlink:title="scalpel" xlink:actuate="onRequest">scalpel</gmx:Anchor>
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            <gco:CharacterString>PI Supplied Instrument Name: scalpel PI Supplied Instrument Description:Samples were collected with a small scalpel. Instrument Name: scalpel Instrument Short Name:   Instrument Description: A scalpel, or lancet, or bistoury, is a small and extremely sharp bladed instrument used for dissection and surgery.</gco:CharacterString>
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                <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/instrument/924758.rdf" xlink:title="Thermo Scientific NanoDrop spectrophotometer" xlink:actuate="onRequest">NanoDrop</gmx:Anchor>
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            <gco:CharacterString>PI Supplied Instrument Name: NanoDrop PI Supplied Instrument Description:DNA quantity and quality were assessed with Nanodrop, Qubit, and gel electrophoresis. Instrument Name: Thermo Scientific NanoDrop spectrophotometer Instrument Short Name:NanoDrop spectrophotometer   Instrument Description: Thermo Scientific NanoDrop spectrophotometers provide microvolume quantification and purity assessments of DNA, RNA, and protein samples. NanoDrop spectrophotometers work on the principle of ultraviolet-visible spectrum (UV-Vis) absorbance. The range consists of the NanoDrop One/OneC UV-Vis Spectrophotometers, NanoDrop Eight UV-Vis Spectrophotometer and NanoDrop Lite Plus UV Spectrophotometer.</gco:CharacterString>
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