Torbjørn Forseth

Dr. Torbjørn Forseth

Department of Aquatic Biodiversity, The Norwegian Institute for Nature Research (NINA), 7034 Trondheim, Norway

Research Focus & Metrics

Academic Career Length

36Years (1991-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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28 November 2017 in Fish and Fisheries
Verified
Journal Article
Open access
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Ana T. SilvaAna T. Silva
Ana T. Silva
MLMartyn C. Lucas
Martyn C. Lucas
TCTheodore Castro-Santos
Theodore Castro-Santos
CKChristos Katopodis
Christos Katopodis
LBLee Baumgartner
Lee Baumgartner
SCSteven J. Cooke
Steven J. Cooke
Much effort has been devoted to developing, constructing and refining fish passage facilities to enable target species to pass barriers on fluvial systems, and yet, fishway science, engineering and practice remain imperfect. In this review, 17 experts from different fish passage research fields (i.e., biology, ecology, physiology, ecohydraulics, engineering) and from different continents (i.e., North and South America, Europe, Africa, Australia) identified knowledge gaps and provided a roadmap for research priorities and technical developments. Once dominated by an engineering‐focused approach, fishway science today involves a wide range of disciplines from fish behaviour to socioeconomics to complex modelling of passage prioritization options in river networks. River barrier impacts on fish migration and dispersal are currently better understood than historically, but basic ecological knowledge underpinning the need for effective fish passage in many regions of the world, including in biodiversity hotspots (e.g., equatorial Africa, South‐East Asia), remains largely unknown. Designing efficient fishways, with minimal passage delay and post‐passage impacts, requires adaptive management and continued innovation. While the use of fishways in river restoration demands a transition towards fish passage at the community scale, advances in selective fishways are also needed to manage invasive fish colonization. Because of the erroneous view in some literature and communities of practice that fish passage is largely a proven technology, improved international collaboration, information sharing, method standardization and multidisciplinary training are needed. Further development of regional expertise is needed in South America, Asia and Africa where hydropower dams are currently being planned and constructed.

3 March 2017 in ICES Journal of Marine Science
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Journal Article
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TFTorbjørn Forseth
Torbjørn Forseth
BBBjørn T. Barlaup
Bjørn T. Barlaup
BFBengt Finstad
Bengt Finstad
PFPeder Fiske
Peder Fiske
HGHarald Gjøsæter
Harald Gjøsæter
VWVidar Wennevik
Vidar Wennevik
Atlantic salmon (Salmo salar) is an economically and culturally important species. Norway has more than 400 watercourses with Atlantic salmon and supports a large proportion of the world’s wild Atlantic salmon. Atlantic salmon are structured into numerous genetically differentiated populations, and are therefore managed at the population level. Long-distance migrations between freshwater and ocean habitats expose Atlantic salmon to multiple threats, and a number of anthropogenic factors have contributed to the decline of Atlantic salmon during the last decades. Knowledge on the relative importance of the different anthropogenic factors is vital for prioritizing management measures. We developed a semi-quantitative 2D classification system to rank the different anthropogenic factors and used this to assess the major threats to Norwegian Atlantic salmon. Escaped farmed salmon and salmon lice from fish farms were identified as expanding population threats, with escaped farmed salmon being the largest current threat. These two factors affect populations to the extent that they may be critically endangered or lost, with a large likelihood of causing further reductions and losses in the future. The introduced parasite Gyrodactylus salaris, freshwater acidification, hydropower regulation and other habitat alterations were identified as stabilized population threats, which have contributed to populations becoming critically endangered or lost, but with a low likelihood of causing further loss. Other impacts were identified as less influential, either as stabilized or expanding factors that cause loss in terms of number of returning adults, but not to the extent that populations become threatened. Management based on population specific reference points (conservation limits) has reduced exploitation in Norway, and overexploitation was therefore no longer regarded an important impact factor. The classification system may be used as a template for ranking of anthropogenic impact factors in other countries and as a support for national and international conservation efforts.

1 July 1999 in Journal of Animal Ecology
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Journal Article
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TFTorbjørn Forseth
Torbjørn Forseth
TNTor F. Nesje
Tor F. Nesje
BJBror Jonsson
Bror Jonsson
KHKarstein Hårsaker
Karstein Hårsaker

20 December 2001 in Functional Ecology
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Journal Article
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BJB. Jonsson
B. Jonsson
TFTorbjørn Forseth
Torbjørn Forseth
AJA. J. Jensen
A. J. Jensen
TNT. F. Næsje
T. F. Næsje
Summary: Experimental data for maximum growth and food consumption of Atlantic Salmon (Salmo salarL.) parr from five Norwegian rivers situated between 59 and 70°N were analysed and modelled. The growth and feeding models were also applied to groups of Atlantic Salmon growing and feeding at rates below the maximum. The data were fitted to the Ratkowsky model, originally developed for bacterial growth. The rates of growth and food consumption varied significantly among populations but the variation appeared unrelated to thermal conditions in the river of population origins. No correlation was found between the thermal conditions and limits for growth, thermal growth optima or maximum growth, and hypotheses of population‐specific thermal adaptation were not supported. Estimated optimum temperatures for growth were between 16 and 20 °C. Model parameter estimates differed among growth‐groups in that maximum growth and the performance breadth decreased from fast to slow growing individuals. The optimum temperature for growth did not change with growth rate. The model for food consumption (expressed in energy terms) peaked at 19–21 °C, which is only slightly higher than the optimal temperature for growth. Growth appeared directly related to food consumption. Consumption was initiated ≈2 °C below the lower temperature for growth and terminated ≈1·5 °C above the upper critical temperature for growth. Model parameter estimates for consumption differed among growth‐groups in a manner similar to the growth models. By combining the growth and consumption models, growth efficiencies were estimated. The maximum efficiencies were high, 42–58%, and higher in rivers offering hostile than benign feeding and growth opportunities.

5 July 2007 in Freshwater Biology
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Journal Article
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AFA. G. Finstad
A. G. Finstad
SES. Einum
S. Einum
TFTorbjørn Forseth
Torbjørn Forseth
OUO. Ugedal
O. Ugedal

1 February 2001 in Freshwater Biology
Verified
Journal Article
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TFTorbjørn Forseth
Torbjørn Forseth
MHM. A. Hurley
M. A. Hurley
AJA. J. Jensen
A. J. Jensen
JEJ. M. Elliott
J. M. Elliott