FY07-09 proposal 200717500

Jump to Reviews and Recommendations

Section 1. Administrative

Proposal titleDNA typing to identify native inland Oncorhynchus mykiss
Proposal ID200717500
OrganizationWashington State University
Short descriptionNew DNA-Based Tests, which distinquish the Inland and Coastal forms of Rainbow Trout will be developed. These tests should be widely useful for genetic characterization of Columbia Basin Populations.
Information transferPublications in Journals and Presentations at Scientific Meetings
Proposal contact person or principal investigator
Contacts
ContactOrganizationEmail
Form submitter
Gary Thorgaard Washington State University thorglab@wsu.edu
All assigned contacts
Dan Nordquist Washington State University ogrd@wsu.edu
Lori Selby Washington State University spfo@wsu.edu
Gary Thorgaard Washington State University thorglab@wsu.edu

Section 2. Locations

Province / subbasin: Mainstem/Systemwide / Systemwide

LatitudeLongitudeWaterbodyDescription

Section 3. Focal species

primary: Interior Redband Trout
secondary: Steelhead All Populations

Section 4. Past accomplishments

YearAccomplishments

Section 5. Relationships to other projects

Funding sourceRelated IDRelated titleRelationship
BPA 200103200 Coeur D'Alene Fisheries Enhanc Involves assessment of genetic purity of native trout.
BPA 199404900 Kootenai River Resident Fish A Involves assessment of genetic purity of redband trout
BPA 198909600 Genetic M&E Prog For Sal/Steel Utilizes genetic markers on an ongoing basis and would benefit from improved marker technology
BPA 199800200 Snake River Native Salmonid As Would benefit from improved DNA marker technology
BPA 200007900 Assess Res Fish Owyhee DVIR Would benefit from DNA marker technologies for identifying purity of redband trout populations
BPA 199701900 Stinking Water Salmonid Projec Malheur River redband trout may have hybridized with introduced rainbow trout.

Section 6. Biological objectives

Biological objectivesFull descriptionAssociated subbasin planStrategy
Assess resident fish losses Identify hybridized populations Boise/Payette/Weiser Determine extent of redband/ rainbow hybridization
Assess resident fish losses Identify hybridized populations Clearwater Redband populations will be identified and typed with DNA marker technology
Assess resident fish losses Identify hybridized populations Bruneau Develop genetic markers to distinguish between native redband trout and nonnative rainbow trout from hatchery origin
Assess resident fish losses Identify hybridized populations Intermountain Determine genetic distribution of resident redband trout (San Poil River)
Assess resident fish losses Identify hybridized populations Intermountain Determine genetic distribution of native focal species, including rainbow/ redband trout (Upper Columbia)
Assess resident fish losses Identify hybridized populations Malheur Genetic evaluation of redband trout to determine degree of integration and hybridization with introduced rainbow trout
Assess resident fish losses Identify hybridized populations Snake Hells Canyon No information is available regarding genetic integrity of redband trout
Assess resident fish losses Identify hybridized populations Walla Walla What is the rate of hybridization between endemic wild and out-of-basin hatchery reared stocks?
Conserve biodiversity in rainbow trout Test patterns of genetic variation Asotin Coordinated assessment of genetic analyses
Conserve biodiversity in rainbow trout Test patterns of genetic variation Burnt Expedite analysis of archived data and encourage additional genetic sampling of redband trout
Conserve biodiversity in rainbow trout Test patterns of genetic variation Fifteenmile Conduct genetic sampling of steelhead returning to Fifteenmile Compare resident trout and steelhead genetics in Fifteenmile Creek Genetic sampling of Mill Creek steelhead
Conserve biodiversity in rainbow trout Test patterns of genetic variation Grande Ronde Determine and compare genetic characteristics of hatchery and natural fish in the Grande Ronde subbasin
Conserve biodiversity in rainbow trout Test patterns of genetic variation Hood Monitor population genetic structure of steelhead and resident rainbow trout
Conserve biodiversity in rainbow trout Test patterns of genetic variation Lower Snake Genetic characterization of steelhead and resident rainbow trout
Conserve biodiversity in rainbow trout Test patterns of genetic variation Middle Snake Continue genetic evaluation of redband trout
Conserve biodiversity in rainbow trout Test patterns of genetic variation Owyhee Assess population structure, including genetic structure, of fish populations on the DVIR.
Conserve biodiversity in rainbow trout Test patterns of genetic variation Powder Expedite analysis of archived data and encourage additional genetic sampling of redband trout.
Conserve biodiversity in rainbow trout Test patterns of genetic variation Salmon Continue collection of life history characteristics and genetic diversity data on focal fish species
Conserve biodiversity in rainbow trout Test patterns of genetic variation Intermountain Perform assessment of native salmonid stocks composition using DNA analysis or other appropriate techniques by 2010 (Spokane system)
Conserve biodiversity in rainbow trout Test patterns of genetic variation Umatilla Assess and monitor the genetic characteristics of natural and hatchery reared steelhead

Section 7. Work elements (coming back to this)

Work element nameWork element titleDescriptionStart dateEnd dateEst budget
Develop RM&E Methods and Designs Develop DNA-based tests for identifying hybrdization and monitoring biodiversity in rainbow trout Tests wil be developed which could replace allozyme tests currently being used. This will facilitate sampling and testing. New DNA tests to differentiate redband and coastal rainbow trout will also be developed. 2/1/2007 9/30/2009 $333,946
Biological objectives
Metrics

Section 8. Budgets

Itemized estimated budget
ItemNoteFY07FY08FY09
Personnel 50% salaries are requested for Joseph Brunelli (assistant research professor) and a research associate to be identified. Funding for an hourly lab employee (10 hours/ week) is also requested. $28,733 $45,080 $46,883
Fringe Benefits [blank] $8,696 $13,570 $14,112
Supplies Costs of molecular biology supplies and DNA sequencing. Allozyme typing costs are included in year one. $16,700 $25,000 $26,000
Travel Travel for sample collection and to attend meetings $670 $1,000 $1,040
Overhead 46.8% TDC $25,646 $39,616 $41,200
Totals $80,445 $124,266 $129,235
Total estimated FY 2007-2009 budgets
Total itemized budget: $333,946
Total work element budget: $333,946
Cost sharing
Funding source/orgItem or service providedFY 07 est value ($)FY 08 est value ($)FY 09 est value ($)Cash or in-kind?Status
Washington State University 5% salary for PI $8,651 $8,997 $9,357 In-Kind Under Review
Totals $8,651 $8,997 $9,357

Section 9. Project future

FY 2010 estimated budget: $0
FY 2011 estimated budget: $0
Comments:

Future O&M costs:

Termination date: 9/30/09
Comments: We expect to publish several papers from this research and to present the results at meetings to share the technology we develop with interested researchers.

Final deliverables: Publications, presentations, and new methods for DNA typing to distinguish inland from coastal rainbow trout, and to detect hybrids.

Section 10. Narrative and other documents


Reviews and recommendations

FY07 budget FY08 budget FY09 budget Total budget Type Category Recommendation
NPCC FINAL FUNDING RECOMMENDATIONS (Oct 23, 2006) [full Council recs]
$0 $0 $0 $0 Expense Basinwide Do Not Fund
NPCC DRAFT FUNDING RECOMMENDATIONS (Sep 15, 2006) [full Council recs]
$0 $0 $0 $0 Basinwide

ISRP PRELIMINARY REVIEW (Jun 2, 2006)

Recommendation: Fundable

NPCC comments: This project proposes to develop suites of molecular genetic markers for discriminating between coastal rainbow trout and inland rainbow trout. The problem of identification and historical mixing and introgression among these O. mykiss forms is identified and pervasive. Current methods based on allozyme polymorphism are inadequate for a number of reasons and beg for more modern approaches (to such age-old questions). The project is fundable as it will develop usable tools for conservation and restoration of native rainbow trout populations. The methods are largely demonstrated as tractable by sponsors, and the applicability throughout the basin is high. The ISRP recommends coordination of this work with studies proposed by IDFG (200721800) to avoid duplication and to enhance overall power of results. Several of the subbasin plans identify the mixing (and potential interbreeding) of these forms to be a current or historical issue needing methods to assess its extent and effects. While, the project will not specifically address any single problem or situation in a subbasin plan, it will provide the means to address these in the future. Ultimately, the project has direct relationship to numerous other genetics-based M&E or research projects. The project has two primary objectives regarding the development of usable and appropriate molecular genetic markers for identifying the level and extent of hybridization between introduced and native rainbow trout in the interior Columbia basin: 1) SNPs that are equivalent to presently available allozyme markers (LDH-B and SOD); and, 2) a suite of new AFLP marker variants associated with the inland and coastal forms. The objectives are part of several subbasin plans. The methods of developing the markers are adequately described and generally appropriate. The proposal will be stronger with the confirmation that populations selected are in fact monophyletic in terms of whether they are coastal or inland (as well as their allozyme genotype). The sponsors should indicate also that number of SNPs or AFLPs that will be targeted for development. Published information indicates that even with fixed differences among groups, at least 8 to 10 loci (or more) characters are needed to discriminate among various hybrid, backcross, and parental lineages in an admixture within a 95% confidence. For characters that are not fixed for alternative alleles or forms (such as with the allozymes) and even greater number is needed. Therefore, figuring the target of SNPs and AFLPs is important from a discriminatory power perspective. As a last minor improvement, the sponsors need to more clearly describe populations to be sampled, and sampling techniques.


ISRP FINAL REVIEW (Aug 31, 2006)

Recommendation: Fundable

NPCC comments: This project proposes to develop suites of molecular genetic markers for discriminating between coastal rainbow trout and inland rainbow trout. The problem of identification and historical mixing and introgression among these O. mykiss forms is identified and pervasive. Current methods based on allozyme polymorphism are inadequate for a number of reasons and beg for more modern approaches (to such age-old questions). The project is fundable as it will develop usable tools for conservation and restoration of native rainbow trout populations. The methods are largely demonstrated as tractable by the sponsors, and the applicability throughout the basin is high. The ISRP recommends coordination of this work with studies proposed by IDFG (200721800) to avoid duplication and to enhance overall power of results. Several of the subbasin plans identify the mixing (and potential interbreeding) of these forms to be a current or historical issue needing methods to assess its extent and effects. While, the project will not specifically address any single problem or situation in a subbasin plan, it will provide the means to address these in the future. Ultimately, the project has direct relationship to numerous other genetics-based M&E or research projects. The project has two primary objectives regarding the development of usable and appropriate molecular genetic markers for identifying the level and extent of hybridization between introduced and native rainbow trout in the interior Columbia basin: 1) SNPs that are equivalent to presently available allozyme markers (LDH-B and SOD); and, 2) a suite of new AFLP marker variants associated with the inland and coastal forms. The objectives are part of several subbasin plans. The methods of developing the markers are adequately described and generally appropriate. The proposal will be stronger with the confirmation that populations selected are in fact monophyletic in terms of whether they are coastal or inland (as well as their allozyme genotype). The sponsors should indicate also that number of SNPs or AFLPs that will be targeted for development. Published information indicates that even with fixed differences among groups, at least 8 to 10 loci (or more) characters are needed to discriminate among various hybrid, backcross, and parental lineages in an admixture within a 95% confidence. For characters that are not fixed for alternative alleles or forms (such as with the allozymes) and even greater number is needed. Therefore, figuring the target of SNPs and AFLPs is important from a discriminatory power perspective. As a last minor improvement, the sponsors need to more clearly describe populations to be sampled, and sampling techniques.