FY07-09 proposal 200711000

Jump to Reviews and Recommendations

Section 1. Administrative

Proposal titleDifferences in Functional Genes Between Hatchery and Wild Chinook Salmon
Proposal ID200711000
OrganizationUniversity of Idaho - Aquaculture Research Institute
Short descriptionThis project will examine functional genetic differences between hatchery and wild Chinook salmon with the goal of identifying and reducing negative hatchery effects through modified hatchery practices.
Information transferInformation gathered and generated during this project will be disseminated via publication in peer-reviewed, scientific journals.
Proposal contact person or principal investigator
Contacts
ContactOrganizationEmail
Form submitter
Madison Powell University of Idaho mpowell@uidaho.edu
All assigned contacts
Tom Flagg NOAA Fisheries, Manchester Research Station tom.flagg@noaa.gov
Ronald Hardy University of Idaho rhardy@uidaho.edu
Madison Powell University of Idaho mpowell@uidaho.edu

Section 2. Locations

Province / subbasin: Mainstem/Systemwide / Systemwide

LatitudeLongitudeWaterbodyDescription
46.4346 117.0142 [none] Aquaculture Research Institute - University of Idaho
42.4535 -114.5122 [none] Hagerman Fish Culture Experiment Station

Section 3. Focal species

primary: Chinook All Populations

Section 4. Past accomplishments

YearAccomplishments

Section 5. Relationships to other projects

Funding sourceRelated IDRelated titleRelationship
[Funding Source left blank] [no entry] [Relationship field left blank]

Section 6. Biological objectives

Biological objectivesFull descriptionAssociated subbasin planStrategy
Quantify differences between hatchery & wild salmo A series of hypothesis-driven, comparative studies of Chinook salmon populations in Idaho, Washington and Oregon will be used to address this objective. These studies are observational and focus on functional genetic differences between hatchery and wild Chinook salmon as observed using DNA microarray data (RM&E Uncertainties Research). None [Strategy left blank]
Reduce differences between hatchery & wild salmon Two hypothesis-driven, manipulative studies will be used to address this objective. This study will examine changes in gene expression in Chinook salmon when subjected to different hatchery protocols. Specifically, the effectiveness of alternative “hatchery reform” practices on reducing differences in gene expression between hatchery and wild fish. None [Strategy left blank]

Section 7. Work elements (coming back to this)

Work element nameWork element titleDescriptionStart dateEnd dateEst budget
Produce/Submit Scientific Findings Report Produce Manuscript of Differential Gene Expression and Functional Testing Produce a peer-reviewed manuscript of experimental findings 7/1/2008 10/31/2009 $0
Biological objectives
Reduce differences between hatchery & wild salmon
Metrics
Produce/Submit Scientific Findings Report Produce Manuscript of Microarray Analyses Produce a peer-reviewed manuscript of experimental findings. 7/1/2008 7/1/2009 $0
Biological objectives
Quantify differences between hatchery & wild salmo
Metrics
Analyze/Interpret Data Analyze and Interpret Functional Testing Analyze and correlate functional testing with bioinformatics data 7/1/2008 10/31/2009 $53,497
Biological objectives
Reduce differences between hatchery & wild salmon
Metrics
Primary R, M, and E Type: Action Effectiveness Research
Analyze/Interpret Data Analyze Microarray and Bioinformatics Data Complete analysis and post-analysis interpretation of differential expression observed using microarrays 7/1/2007 7/1/2009 $250,516
Biological objectives
Quantify differences between hatchery & wild salmo
Metrics
Primary R, M, and E Type: Uncertainties Research
Analyze/Interpret Data Analyze Microarray and Bioinformatics Data Analyze and interpret all microarray, RT-PCR and bioinformatics data. 7/1/2007 10/31/2009 $498,067
Biological objectives
Reduce differences between hatchery & wild salmon
Metrics
Primary R, M, and E Type: Uncertainties research
Collect/Generate/Validate Field and Lab Data Collect and analyze Chinook salmon smolts Both hatchery and wild Chinook salmon smolts will be collected during outmigration at four locations. Tissues from samples will then be analyzed using DNA microarrays. 5/1/2007 10/31/2009 $306,187
Biological objectives
Quantify differences between hatchery & wild salmo
Metrics
Primary R, M, and E Type: Uncertainties research
Collect/Generate/Validate Field and Lab Data Culture, Sample and Analyze Chinook salmon Chinook salmon from two locations will be cultured under two separate hatchery protocols. Samples will be taken and analyzed for differential gene expression using QPCR and for physiological differences. 9/1/2007 10/31/2009 $163,257
Biological objectives
Reduce differences between hatchery & wild salmon
Metrics
Primary R, M, and E Type: Action Effectiveness Research
Collect/Generate/Validate Field and Lab Data Functional Testing Functional testing of cultured, experimental and control fish. 7/1/2007 10/31/2009 $317,902
Biological objectives
Reduce differences between hatchery & wild salmon
Metrics
Primary R, M, and E Type: Action Effectiveness Research

Section 8. Budgets

Itemized estimated budget
ItemNoteFY07FY08FY09
Personnel Principal Investigator - Ron Hardy $10,818 $11,251 $11,700
Personnel Co-P.I. - Matt Powell $7,265 $7,557 $7,858
Personnel Co-P.I. - Barrie Robison $5,275 $5,485 $5,703
Personnel Co-P.I. - Rod Hill $5,687 $5,913 $6,151
Personnel Post-doctoral Fellow $44,720 $46,509 $48,360
Personnel Scientific Aide - Joyce Faler $25,490 $26,520 $13,790
Personnel Scientific Aide - Churchill $10,768 $14,560 $7,571
Personnel Graduate Student $21,632 $22,495 $23,400
Personnel Hourly Student Labor $13,000 $13,520 $14,061
Fringe Benefits Principal Investigator - Hardy $3,570 $3,713 $3,861
Fringe Benefits Co-P.I. - Powell $2,398 $2,494 $2,593
Fringe Benefits Co-P.I. - Robison $1,846 $1,920 $1,996
Fringe Benefits Co-P.I. - Hill $1,933 $2,011 $2,091
Fringe Benefits Post-doctoral Fellow $15,652 $16,278 $16,926
Fringe Benefits Scientific Aide - Faler $8,922 $9,282 $4,827
Fringe Benefits Sicentific Aide - Churchill $4,953 $6,698 $3,483
Fringe Benefits Graduate Student $130 $135 $141
Fringe Benefits Hourly Student Labor $1,170 $1,217 $1,265
Supplies Lab supplies for genetic analyses $32,000 $48,000 $27,200
Supplies Microarry chips @$120 ea. $48,000 $72,000 $40,800
Supplies Functional testing @ $100/fish $11,000 $19,000 $6,000
Supplies Tank and fish rearing supplies $3,000 $6,000 $6,000
Supplies RT-PCR supplies $0 $7,500 $12,500
Travel Regional travel for project $6,000 $6,000 $4,000
Travel National travel to scientific meetings $4,000 $4,000 $3,000
Other Subcontract - CRITFC $2,500 $20,000 $20,000
Other Subcontract - IDFG $20,000 $20,000 $20,000
Other Subcontract - ODFW $2,500 $20,000 $20,000
Other Subcontract - WDFW $20,000 $20,000 $20,000
Other Subcontract - NOAA Fisheries $25,000 $25,000 $30,000
Overhead Facilities and Administrative Rates @31.5% $112,789 $146,109 $120,964
Personnel Co-P.I. - Tom Flagg $0 $0 $0
Personnel Co-P.I. - Paul Kline $0 $0 $0
Personnel Co.-P.I. - Paul Seidel $0 $0 $0
Totals $472,018 $611,167 $506,241
Total estimated FY 2007-2009 budgets
Total itemized budget: $1,589,426
Total work element budget: $1,589,426
Cost sharing
Funding source/orgItem or service providedFY 07 est value ($)FY 08 est value ($)FY 09 est value ($)Cash or in-kind?Status
CRITFC sample collection/research $1,250 $8,571 $8,182 In-Kind Confirmed
IDFG sample collection/research $10,000 $8,571 $8,182 In-Kind Confirmed
National Science Foundation Capital Equipment $25,000 $0 $0 In-Kind Confirmed
NOAA-Fisheries sample colleciton/research $12,500 $10,714 $12,273 In-Kind Confirmed
ODFW sample collection/research $1,250 $8,571 $8,182 In-Kind Confirmed
University of idaho Salaries $24,052 $25,013 $26,012 In-Kind Confirmed
WDFW sample collection/research $10,000 $8,571 $8,182 Cash Confirmed
Totals $84,052 $70,011 $71,013

Section 9. Project future

FY 2010 estimated budget: $0
FY 2011 estimated budget: $0
Comments: No outyear funds are requested.

Future O&M costs:

Termination date: 10/31/09
Comments: All objectives will be complete by 10/31/09

Final deliverables: Final deliverables include manuscript(s) submitted for peer-review in scientific journals.

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: Response requested

NPCC comments: Although the technique proposed for use in this proposal is potentially a very valuable tool, the ISRP does not recommend funding the proposal as worded. The ISRP believes that the utility of the technique as it stands now is more uncertain than portrayed, and the proposal needs to provide further explanation. The proposal should acknowledge that baseline data are needed to determine how the results of the micro array assays should be interpreted. For example, it should be acknowledged that an individual fish raised in different environments would give different assay results -- but how different, and how would the authors interpret those different array assays? The technical aspects of gene chip arrays and the molecular methods are well developed. We question the actual experimental design in some cases, however, as being sound enough to test what is being proposed. For example, it is assumed that a result showing that gene expression differences have become similar (as measured by quantification of expression at a molecular level) means that "for the purposes of evolutionary fitness, the hatchery environment can then serve as a surrogate to the natural environment for rearing salmon and steelhead." We don’t believe that such a level of cause/effect has ever been shown. It is still a long way from similarity in micro array results to fitness equality. The underlying approach of this proposal may be inadequate and should be further justified in a response. The ISRP also feels that there is a need to identify how application to management will occur or at least to demonstrate how communication with the relevant management agencies would occur. Technical and scientific background: There is quite a bit of technical background given on the potential of this new technique, but we are not convinced that the authors are fairly stating what it will or will not be able to answer. There is substantial muddling of the concerns regarding the inherent genetic differences between stocked and wild spawned fish (including issues associated with inbreeding and out breeding depression) with those of how rearing a fish in a hatchery environment can change its phenotypic expression of genes, resulting in an organism that looks, behaves, performs differently than if it were raised in the wild. A clear explanation of how this technique can or cannot address those two quite different questions is needed. It is not evident from the authors' explanation that this difference is clearly appreciated and understood. Rationale and significance to subbasin plans and regional programs: In concept, the problem addressed (hatchery vs. wild differences) is an important issue. The relationship of the proposal to subbasin plans and regional programs is explained only superficially. In addition, as is pervasive throughout this proposal, there is substantial overstatement of the potential impacts of the results. As an example, "The proposed project offers to add a new dimension to our understanding of factors that affect differences in hatchery and wild fish by determining the functional role of differentially expressed genes." The ISRP is not convinced that it will be all that easy or clear - much less accomplishable within this timeframe. Relationships to other projects: Although the proposal states, "The proposed project will provide information to support most artificial propagation programs in the Columbia River Basin," few details are given and no other projects are identified on the cover proposal or narrative. Objectives: Objectives are concise and have nice sets of alternative hypotheses, but eventual applicability to management is unclear. Tasks (work elements) and methods: Innovative approaches to assessing the functional differences between hatchery and wild fish are proposed, which may at some time serve to assess reforms in hatchery rearing protocols. It is just not clear, however, that without substantial basic research on what the assays are telling us, that the technique will be able to answer those questions. Monitoring and evaluation: This is a proposal to develop assessment technology. If it works it could make a significant contribution to deciding whether hatchery practices can be modify sufficiently to make hatchery production compatible with the need to protect natural populations. It is not clear, however, how the results will be interpreted nor how they will be used to change management strategies. Facilities, equipment, and personnel: This laboratory seems to be an excellent venue for such studies, but until we see a response that uses better evolutionary bases for the experimental design, together with a more realistic set of expectations of the technique, we question the level of understanding by the personnel. Information transfer: The sponsors have a track record of publishing the findings of their work in the peer-reviewed literature and producing annual reports, and presenting at regional and national conferences. Benefits to focal and non-focal species: A successful project could affect the focal species positively. However, if the (simplistic?) approach of assuming that array assay similarity translates into fitness/genetic equivalence is transferred to field applications prematurely, there could be risk for harm to the focal species. Until an adequate response is provided, we remain concerned over this possibility. We are not certain there is much of an effect on non-focal species, unless a misinterpretation of results allows rampant stocking.


ISRP FINAL REVIEW (Aug 31, 2006)

Recommendation: Response requested

NPCC comments: Although the technique proposed for use in this proposal is potentially a very valuable tool, the ISRP does not recommend funding the proposal as worded. The ISRP believes that the utility of the technique as it stands now is more uncertain than portrayed, and the proposal needs to provide further explanation. The proposal should acknowledge that baseline data are needed to determine how the results of the micro array assays should be interpreted. For example, it should be acknowledged that an individual fish raised in different environments would give different assay results -- but how different, and how would the authors interpret those different array assays? The technical aspects of gene chip arrays and the molecular methods are well developed. We question the actual experimental design in some cases, however, as being sound enough to test what is being proposed. For example, it is assumed that a result showing that gene expression differences have become similar (as measured by quantification of expression at a molecular level) means that "for the purposes of evolutionary fitness, the hatchery environment can then serve as a surrogate to the natural environment for rearing salmon and steelhead." We don’t believe that such a level of cause/effect has ever been shown. It is still a long way from similarity in micro array results to fitness equality. The underlying approach of this proposal may be inadequate and should be further justified in a response. The ISRP also feels that there is a need to identify how application to management will occur or at least to demonstrate how communication with the relevant management agencies would occur. Technical and scientific background: There is quite a bit of technical background given on the potential of this new technique, but we are not convinced that the authors are fairly stating what it will or will not be able to answer. There is substantial muddling of the concerns regarding the inherent genetic differences between stocked and wild spawned fish (including issues associated with inbreeding and out breeding depression) with those of how rearing a fish in a hatchery environment can change its phenotypic expression of genes, resulting in an organism that looks, behaves, performs differently than if it were raised in the wild. A clear explanation of how this technique can or cannot address those two quite different questions is needed. It is not evident from the authors' explanation that this difference is clearly appreciated and understood. Rationale and significance to subbasin plans and regional programs: In concept, the problem addressed (hatchery vs. wild differences) is an important issue. The relationship of the proposal to subbasin plans and regional programs is explained only superficially. In addition, as is pervasive throughout this proposal, there is substantial overstatement of the potential impacts of the results. As an example, "The proposed project offers to add a new dimension to our understanding of factors that affect differences in hatchery and wild fish by determining the functional role of differentially expressed genes." The ISRP is not convinced that it will be all that easy or clear - much less accomplishable within this timeframe. Relationships to other projects: Although the proposal states, "The proposed project will provide information to support most artificial propagation programs in the Columbia River Basin," few details are given and no other projects are identified on the cover proposal or narrative. Objectives: Objectives are concise and have nice sets of alternative hypotheses, but eventual applicability to management is unclear. Tasks (work elements) and methods: Innovative approaches to assessing the functional differences between hatchery and wild fish are proposed, which may at some time serve to assess reforms in hatchery rearing protocols. It is just not clear, however, that without substantial basic research on what the assays are telling us, that the technique will be able to answer those questions. Monitoring and evaluation: This is a proposal to develop assessment technology. If it works it could make a significant contribution to deciding whether hatchery practices can be modify sufficiently to make hatchery production compatible with the need to protect natural populations. It is not clear, however, how the results will be interpreted nor how they will be used to change management strategies. Facilities, equipment, and personnel: This laboratory seems to be an excellent venue for such studies, but until we see a response that uses better evolutionary bases for the experimental design, together with a more realistic set of expectations of the technique, we question the level of understanding by the personnel. Information transfer: The sponsors have a track record of publishing the findings of their work in the peer-reviewed literature and producing annual reports, and presenting at regional and national conferences. Benefits to focal and non-focal species: A successful project could affect the focal species positively. However, if the (simplistic?) approach of assuming that array assay similarity translates into fitness/genetic equivalence is transferred to field applications prematurely, there could be risk for harm to the focal species. Until an adequate response is provided, we remain concerned over this possibility. We are not certain there is much of an effect on non-focal species, unless a misinterpretation of results allows rampant stocking.