Contributors | Affiliation | Role |
---|---|---|
Tepolt, Carolyn | Woods Hole Oceanographic Institution (WHOI) | Principal Investigator |
Grason, Emily | Sea Grant (WSG) | Co-Principal Investigator |
McDonald, Patrick | University of Washington (UW) | Co-Principal Investigator |
Mickle, Audrey | Woods Hole Oceanographic Institution (WHOI BCO-DMO) | BCO-DMO Data Manager |
Samples of Carcinus maenas (urn:lsid:marinespecies.org:taxname:107381) were collected by large network of collaborators, usually by trapping but approaches vary. Heart tissue was dissected from crabs after severing the ventral nerve cord, and hearts were preserved in RNALater and frozen at -80 prior to extraction. Total RNA extraction was conducted with TRI reagent and 1-bromo-3-chloropropane. mRNA libraries were prepared with Illumina TruSeq Stranded mRNA kits and individually single-indexed with Illumina index sets A and B. Samples were multiplexed 24 / lane of 150 bp pe Illumina HiSeq4000 sequencing at Azenta (formerly Genewiz; South Plainfield NJ).
Samples were demultiplexed by Azenta (formerly Genewiz; South Plainfield NJ), and are provided raw with no further processing.
- Imported "BCO-DMO_RNASeq_metadata_NSF-1850996.csv" into the BCO-DMO system
- Converted date field to ISO UTC format YYYY-MM-DD
- Replaced non-standard character '’' with '''
- Exported file as "949682_v1_green_crabs_rna_seq.csv"
Accepted species identifier confirmed on 2025-01-29.
Parameter | Description | Units |
sample_name | Individual sample ID | unitless |
SRA_accession | SRA accession number for individual sequence files | unitless |
biosample_accession | Individual NCBI BioSample code | unitless |
embayment | General coastal water body from which sample was collected | unitless |
site | More specific data on collection location provided by collector | unitless |
state | US state or Canadian province where samples was collected | unitless |
sex | Sex (M=Male, F=Female, or U=Unknown) | unitless |
size_CW | Carapace width of crab in mm | Millimeters (mm) |
color | Color of ventral side of cephalothorax, as determined by collector | unitless |
collection_date | Date of collection | unitless |
latitude | Latitude of collection; positive values = North | decimal degrees |
longitude | Longitude of collection; positive values = East | decimal degrees |
collector | Person who collected the sample | unitless |
collector_affiliation | Organization through which the sample was collected | unitless |
Dataset-specific Instrument Name | Illumina HiSeq4000 sequencers |
Generic Instrument Name | Automated DNA Sequencer |
Dataset-specific Description | Samples were sequenced using Illumina HiSeq4000 sequencers by Azenta (formerly Genewiz; South Plainfield NJ). |
Generic Instrument Description | General term for a laboratory instrument used for deciphering the order of bases in a strand of DNA. Sanger sequencers detect fluorescence from different dyes that are used to identify the A, C, G, and T extension reactions. Contemporary or Pyrosequencer methods are based on detecting the activity of DNA polymerase (a DNA synthesizing enzyme) with another chemoluminescent enzyme. Essentially, the method allows sequencing of a single strand of DNA by synthesizing the complementary strand along it, one base pair at a time, and detecting which base was actually added at each step. |
NSF Award Abstract:
Marine invasive species pose a serious and ongoing risk to ocean ecosystems and the economies that rely on them. Understanding how such species adapt rapidly to new environments is key to preventing and managing invasions. Traditionally, the focus has been on inherent traits and flexibility of an invasive species, ignoring the potential for evolutionary change after introduction. However, recent research has shown that some marine species may evolve specific genomic features which allow highly efficient selection over as little as a single generation. This project tests the importance of genomic traits in allowing marine invasive species to survive and thrive on new shores. Its focus is on the high-impact invasive European green crab, which has spread over 1,500 km of the West Coast of North America since 1989 and has very recently begun expanding into the Salish Sea. This project tracks the earliest stages of green crab invasion into a new environment where the species is predicted to have substantial ecological and economic impacts. Genetic differences are followed over time and space across the entire West Coast, with a focus on crabs found in the Salish Sea where the species is currently expanding. Genetic data is complemented by oceanographic modeling to predict the spread of green crabs into the Salish Sea and across the West Coast. Finally, targeted sequencing and prior sampling are used to probe the genomic traits underlying these changes and determine if the same traits have played a role in the species' invasive success on other shores. Sampling for this project is conducted by Washington Sea Grant's Crab Team, an expansive outreach and monitoring program powered largely by hundreds of volunteers who monitor green crabs across 3,000 miles of coastline in the Salish Sea. The results of this project are shared with these volunteers and other stakeholders and is used to inform trans-boundary green crab management and spread prediction on the West Coast.
Recent work has hypothesized that genomic architecture, which has been increasingly discovered to play a role in local adaptation, may also be key to a species' ability to adapt quickly when gene flow is high. This project integrates multiple approaches to track the speed and dynamics of adaptation-with-gene flow across a thermal gradient in an explicit oceanographic context using the invasive European green crab (Carcinus maenas). Prior work in this system identified a suite of genes that appear to constitute balanced polymorphisms whose allele frequencies correlate strongly with site temperature against a homogeneous neutral genetic background. This project has three main goals: 1) To examine fine-scale selection to temperature over a comprehensive spatial and temporal data set comprising most of the species' history on the West Coast, 2) To track the expanding range front in the Salish Sea, comparing the genetic trajectory of individuals at the range edge with oceanographic modeling of dispersal, and 3) To characterize the genomic regions surrounding putative balanced polymorphisms and examine the ubiquity of their association with temperature across globally replicated populations. This coupled evolutionary oceanography approach represents an unprecedented test of the speed and nature of rapid adaptation in a highly dynamic natural marine environment.
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) | |
NSF Division of Ocean Sciences (NSF OCE) |