| Contributors | Affiliation | Role |
|---|---|---|
| Bay, Rachael | University of California-Davis (UC Davis) | Principal Investigator |
| Grosberg, Richard K. | University of California-Davis (UC Davis) | Co-Principal Investigator |
| Sanford, Eric | University of California-Davis (UC Davis) | Co-Principal Investigator |
| Cameron, Brenda | University of California-Davis (UC Davis) | Scientist |
| Fenberg, Philip | University of Southampton | Scientist |
| Nielsen, Erica | University of California-Davis (UC Davis) | Scientist |
| Paz-García, David A | Center for Biological Research of the Northwest, SC (CIBNOR) | Scientist |
| Sones, Jacqueline | University of California-Davis (UC Davis) | Scientist |
| Walkes, Samuel | University of California-Davis (UC Davis) | Student |
| Mickle, Audrey | Woods Hole Oceanographic Institution (WHOI BCO-DMO) | BCO-DMO Data Manager |
We sampled 19 sites on the Pacific coast of North America, spanning most of the contemporary range of Lottia gigantea (urn:lsid:marinespecies.org:taxname:456593). 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 >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 & Murray, 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). 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 al. (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.
The data included here are sample data taken directly in the field and summary data for whole genome data, before any processing or analysis.
- Loaded Lottia_metadata.xlsx into BCO-DMO system
- Loaded Lottia_reads.cov.xlsx into BCO-DMO system
- Converted lottia_metadata-1 field date from %m/%d/%y to %Y-%m-%d
- Inner-joined lottia_reads.cov-1 (target) with lottia_metadata-1 (source) on key Library Name
- Set data types in lottia_reads.cov-1: % Dups number; % GC integer; Read Length number; M Seqs number; mill integer; #reads number (scientific notation output); read length integer; read X read length number (scientific notation output); genome size number (scientific notation output); Cov number; latitude number; longitude number; size number; size_group string; date date with format %Y-%m-%d
- Renamed multiple fields: "Library Name" → Library_Name, "Sample ID" → Sample_ID, "% Dups" → Percent_Dups, "% GC" → Percent_GC, "Read_Length" → Average_read_length, "M Seqs" → M_Seqs, "#reads" → num_reads, "read_length" → sequencer_read_length , "read X read length" → read_X_read_length, "genome size" → 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.
| File |
|---|
958640_v1_lottia_genome.csv (Comma Separated Values (.csv), 163.37 KB) MD5:64f8edc9c83061133a1195e89d07ef07 Primary data file for dataset ID 958640, version 1 |
| Parameter | Description | Units |
| Library_Name | Library Name | unitless |
| Sample_ID | Sample ID | unitless |
| Percent_Dups | Percent of reads that are PCR duplicates | percent |
| Percent_GC | GC content (%) for DNA sequences | percent |
| Average_read_length | Average realized read length | base pairs (bp) |
| M_Seqs | Number of reads (in millions) | million reads (10^6 reads) |
| mill | Constant value (1,000,000) used to scale read counts during processing | unitless |
| num_reads | Total number of reads (e.g., M_Seqs × 1,000,000). | unitless |
| sequencer_read_length | Read length of flow cell (150 bp) | base pairs (bp) |
| read_X_read_length | Number of base pairs sequenced (num_reads × read_length) | base pairs (bp) |
| genome_size | Total length of L. gigantea genome measured in base pairs (bp) | base pairs (bp) |
| Cov | Estimated mean sequencing depth (× coverage) across the genome for the sample/library (total bases / genome size) | unitless |
| site | Site name of sampling | unitless |
| date | Date of sampling | unitless |
| latitude | Latitude of sampling, South is negative | decimal degrees |
| longitude | Longitude of sampling, East is positive | decimal degrees |
| size | Shell length/size (mm) measured | mm |
| size_group | Binned sizes used to infer settlement time relative to the 2014–2016 marine heatwaves (e.g., small 10–25 mm, medium 30–40 mm, large >40 mm) | unitless |
| Dataset-specific Instrument Name | DNBSEQ-T7 PE150 platform |
| Generic Instrument Name | Automated DNA Sequencer |
| Dataset-specific Description | Whole genome samples were sequenced at BGI Genomics on a DNBSEQ-T7.
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. |
| Generic Instrument Description | A DNA sequencer is an instrument that determines the order of deoxynucleotides in deoxyribonucleic acid sequences. |
| Dataset-specific Instrument Name | High Sensitivity DNA Bioanalyzer chip |
| Generic Instrument Name | Bioanalyzer |
| Dataset-specific Description | 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. |
| Generic Instrument Description | A Bioanalyzer is a laboratory instrument that provides the sizing and quantification of DNA, RNA, and proteins. One example is the Agilent Bioanalyzer 2100. |
| Dataset-specific Instrument Name | Qubit |
| Generic Instrument Name | Fluorometer |
| Dataset-specific Description | DNA quantity and quality were assessed with Nanodrop, Qubit, and gel electrophoresis. |
| Generic Instrument Description | A fluorometer or fluorimeter is a device used to measure parameters of fluorescence: its intensity and wavelength distribution of emission spectrum after excitation by a certain spectrum of light. The instrument is designed to measure the amount of stimulated electromagnetic radiation produced by pulses of electromagnetic radiation emitted into a water sample or in situ. |
| Dataset-specific Instrument Name | scalpel |
| Generic Instrument Name | scalpel |
| Dataset-specific Description | Samples were collected with a small scalpel. |
| Generic Instrument Description | A scalpel, or lancet, or bistoury, is a small and extremely sharp bladed instrument used for dissection and surgery. |
| Dataset-specific Instrument Name | NanoDrop |
| Generic Instrument Name | Thermo Scientific NanoDrop spectrophotometer |
| Dataset-specific Description | DNA quantity and quality were assessed with Nanodrop, Qubit, and gel electrophoresis. |
| Generic 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. |
NSF abstract:
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.
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.
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.
| Funding Source | Award |
|---|---|
| NSF Division of Ocean Sciences (NSF OCE) |