Abstract
California contains the southernmost native populations of most Pacific Coast salmon and trout, many of which appear to be rapidly headed toward extinction. A quantitative protocol was developed to determine conservation status of all salmonids native to the state. Results indicate that if present trends continue, 25 (78%) of the 32 taxa native to California will likely be extinct or extirpated within the next century, following the bull trout (Salvelinus confluentus), which was extirpated in the 1970s. California’s salmonids are adapted to living in a topographically diverse region with a Mediterranean climate, characterized by extreme seasonal and inter-annual variability in streamflow. Consequently, California salmonids have evolved extraordinary life history diversity to persist in the face of stressful conditions that often approach physiological limits. The spatial distributions of California salmonids vary from wide-ranging anadromous forms to endemic inland forms persisting in only a few kilometers of stream. Eighty-one percent of anadromous taxa are threatened with extinction and 73% inland taxa are either threatened or already extinct. Although specific drivers of decline differ across species, major causes of decline are related to increasing competition with humans for water, human degradation of watersheds, and adverse effects of hatchery propagation. Climate change, interacting with the other causes of decline, is increasing the trajectory towards extinction for most populations. Bringing all of California’s salmonid fishes back from the brink of extinction may not be possible. If there are bold changes to management policy, however, self-sustaining populations of many species may be possible due to their inherent ability to adapt to changing conditions.
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References
Akari H, Arden W, Olsen E, Cooper B, Blouin M (2007a) Reproductive success of captive-bred steelhead trout in the wild: evaluation of three hatchery programs in the Hood River. Conserv Biol 21:181–190
Akari H, Cooper B, Blouin M (2007b) Genetic effects of captive breeding cause a rapid, cumulative fitness decline in the wild. Science 318:100
Akari H, Berejikian B, Ford M, Blouin M (2008) Fitness of hatchery-reared salmonids in the wild. Evol Appl 1:342–355
Akari H, Cooper B, Blouin M (2009) Carry-over effect of captive breeding reduces reproductive fitness of wild-born descendants in the wild. Biol Lett 5:621
Allendorf FW, Ryman N (1987) Genetic management of hatchery stocks. In: Ryman N, Utter F (eds) Population genetics and fishery management. Univ Washington Pr, Seattle, pp 141–159
Allendorf FW, Waples RS (1996) Conservation and genetics of Salmonid fishes. Conservation genetics: case histories from nature, pp 238–280
Beamish RJ (1993) Climate and exceptional fish production off the West Coast of North America. Can J Fish Aquat Sci 50:2270–2291
Beamish RJ, Nevile CEM, Cass AJ (1997) Production of Fraser River sockeye salmon (Oncorhynchus nerka) in relation to decadal-scale changes in the climate and the ocean. Can J Fish Aquat Sci 54:543–554
Behnke RJ (2002) Trout and salmon of North America. Free Press, New York, p 359
Bisson PA, Coutant CC, Goodman D, Gramling R, Lettenmaier D, Lichatowich J, Liss W, Loudenslager E, McDonald L, Philipp D (2002) Hatchery surpluses in the Pacific Northwest. Fisheries 27:16–27
Brett JR (1971) Energetic responses of salmon to temperature. A Study of some thermal relations in the physiology and freshwater ecology of sockeye salmon (Oncorhynchus nerka). Am Zool 11:99–113
Brown LR, Moyle PB, Yoshiyama RM (1994) Historical decline and current status of Coho salmon in California. N Am J Fish Manag 14:237–261
Brown DK, Echelle AA, Propst DL, Brooks JE, Fisher WL (2001) Catastrophic wildfire and number of populations as factors influencing risk of extinction for Gila trout (Oncorhynchus gilae). West N Am Nat 61:139–148
California Data Exchange Center (2009) Klamath River watershed historical precipitation and outflows. In: Calif Dep Water Resouces (ed)
Carmona-Catot G, Moyle PB, Simmons RE (2011) Long-term captive breeding does not necessarily prevent reestablishment: lessons learned from Eagle Lake rainbow trout. Rev Fish Biol Fisheries. Published online 8-28-2011
Carr ME (2001) Estimation of potential productivity in eastern boundary currents using remote sensing. Deep-Sea Res 49:59–80
Carlson SM, Satterthwaite WH, Fleming IA (2011) Weakened portfolio effect in a collapsed salmon population complex. Can J Fish Aquat Sci 68:1579–1589
Cayan D, Bromirski P, Hayhoe K, Tyree M, Dettinger M, Flick R (2008) Climate change projections of sea level extremes along the California coast. Clim Chang 87:57–73
Chilcote MW, Leider SA, Loch JJ (1986) Differential reproductive success of hatchery and wild summer-run steelhead under natural conditions. Trans Am Fish Soc 115:726–735
Chilcote M, Goodson K, Falcy M (2011) Reduced recruitment performance in natural populations of anadromous salmonids associated with hatchery-reared fish. Can J Fish Aquat Sci 68:511–522
Coronado C, Hilborn R (1998) Spatial and temporal factors affecting survival in coho salmon (Oncorhynchus kisutch) in the Pacific Northwest. Can J Fish Aquat Sci 55:2067–2077
Crozier LG, Zabel RW, Hamlet AF (2008) Predicting differential effects of climate change at the population level with life-cycle models of spring Chinook salmon. Global Change Biol 14:236–249
DiLorenzo E, Schneider N, Cobb KM, Franks PJS, Chhak K, Miller AJ, McWilliams JC, Bograd SJ, Arango H, Curchitser E, Powell TM, Rivière P (2008) North Pacific Gyre Oscillation links ocean climate and ecosystem change. Geophys Res Lett 35:6
Dunham JB, Pilliod DS, Young MK (2004) Assessing the consequences of nonnative trout in headwater ecosystems in western North America. Fish 29:18–26
Ebersole JL, Liss WJ, Frissell CA (2001) Relationship between stream temperature, thermal refugia and rainbow trout Oncorhynchus mykiss abundance in arid-land streams in the northwestern United States. Ecol Freshwat Fish 10:1–10
Flick WA, Webster DA (1964) Comparativ first year survival and production in wild and domestic strains of brook trout, Salvelinus fontinalis. Trans Am Fish Soc 93:58–69
Ford MJ (2002) Selection in captivity during supportive breeding my reduce fitness in the wild. Conserv Bio 16:815–825
Galbraith H, Jones R, Park R, Clough J, Herrod-Julius S, Harrington B, Page G (2002) Global climate change and sea level rise: potential losses of intertidal habitat for shorebirds. Waterbirds 25:173–183
Goodman D (2005) Selection equilibrium for hatchery and wild spawning fitness in integrated breeding programs. Can J Fish Aquat Sci 62:374–389
Greene CW (1952) Results from stocking brook trout of wild and hatchery strains at Stillwater Pond. Trans Am Fish Soc 81:43–52
Greene CM, Hall JE, Guilbault KR, Quinn TP (2010) Improved viability of populations with diverse life-history portfolios. Biol Lett 6(3):382–386
Gresswell RE (1999) Fire and aquatic ecosystems in forested biomes of North America. Trans Am Fish Soc 128:193–221
Hamlet AF, Mote PW, Clark MP, Lettenmaier DP (2005) Effects of temperature and precipitation variability on snowpack trends in the western United States. J Clim 18:4545–4561
Hanak E, Lund J, Dinar A, Gray B, Howitt R, Mount J, Moyle P, Thompson B (2011) Managing California’s water: from conflict to reconciliation. Public Policy Inst Calif, San Francisco
Hare SR, Francis RC (1995) Climate change and salmon production in the northeast Pacific Ocean. In: Beamish RJ (ed) Climate change and northern fish populations. National Research Council Canada, Ottowa, pp 357–372
Hauri C, Gruber N, Plattner GK, Alin S, Feely RA, Hales B, Wheeler PA (2009) Ocean acidification in the California current system. Ocean 22:60–71
Hayhoe K, Cayan D, Field CB, Frumhoff PC, Maurer EP, Miller NL, Moser SC, Schneider SH, Cahill KN, Cleland EE, Dale L, Drapek R, Hanemann M, Kalkstein LS, Lenihan J, Lunch CK, Neilson RP, Sheridan SC, Verville JH (2004) Emissions pathways, climate change, and impacts on California. Proc Natl Acad Sci 101:12422–12427
Hays GC, Richardson AJ, Robinson C (2005) Climate change and marine plankton. Trends Ecol Evol 20:337–344
Heard WR (1998) Do hatchery salmon affect the North Pacific Ocean ecosystem? NPa. Anadr Fish Comm Bull 1:405–411
Hilborn R, Quinn TP, Schindler DE, Rogers DE (2003) Biocomplexity and fisheries sustainability. Proc Natl Acad Sci USA 100:6564–6568
Intergovernmental Panel for Climate Change (2007) Climate Change 2007: The Physical Science Basis, Contribution of Working Group I to the Fourth Assessment Report of the Intergovernmental Panel on Climate Change. In: Solomon et al. (ed), Cambridge Univ. Pr, Cambridge, UK
Isaak DJ, Thurow RF, Rieman BE, Dunham JB (2007) Chinook salmon use of spawning patches: relative roles of habitat quality, size, and connectivity. Eco Appl 17:352–364
JMP, Version 9 (2011) SAS Institute Inc., Cary, NC
Kaeriyama M, Nakamura M, Edapalina R, Bower J, Yamaguchi H, Walker R, Myers K (2004) Change in feeding ecology and trophic dynamics of Pacific salmon (Oncorhynchus spp) in the central Gulf of Alaska in relation to climate events. Fish Ocean 13:197–207
Knowles N, Cayan DR (2002) Potential effects of global warming on the Sacramento/San Joaquin watershed and the San Francisco estuary. Geophys Res Lett 29:1891–1894
Krkosek M, Lewis MA, Volpe JP (2005) Transmission dynamics of parasitic sea lice from farm to wild salmon. Proc R Soc B 272:689–696
Kostow K (2009) Factors that contribute to the ecological risks of salmon and steelhead hatchery programs and some mitigating strategies. Rev Fish Biol Fish 19:9–31
Lackey RT, Lach D, Duncan S (eds) (2006) Salmon 2100: the future of wild Pacific salmon. American Fisheries Society, Bethesda, Maryland, p 629
Lehodey P, Alheit J, Barange M, Baumgartner T, Beaugrand G, Drinkwater K, Fromentin J-M, Hare SR, Ottersen G, Perry RI, Roy C, Lingen C, Werneri F (2006) Climate variability, fish and fisheries. J Clim 19:5009–5030
Levin PS, Williams JG (2002) Interspecific effects of artificially propagated fish: an additional conservation risk for salmon. Conserv Bio 16:1581–1587
Levin PS, Zabel RW, Williams JG (2001) The road to extinction is paved with good intentions: negative association of fish hatcheries with threatened salmon. Proc Royal Soc London, Series B: Bio Sci 268:1153
Lindley ST, Grimes CB, Mohr MS, Peterson WT, Stein JE, Anderson JJ, Botsford LW, Bottom DL, Busack CA, Collier TK (2009) What caused the Sacramento River fall Chinook stock collapse? US Dept of Commerce, National Oceanic and Atmospheric Administration, National Marine Fisheries Service, Southwest Fisheries Science Center, Fisheries Ecology Division
Lund J, Hanak E, Fleenor W, Howitt R, Mount J, Moyle P (2007) Envisioning futures for the Sacramento-San Joaquin Delta. Public Policy Institute of California, San Francisco
Lynch M, Healy M (2001) Captive breeding and the genetic fitness of natural populations. Conserv Genet 2:363–378
Mantua NJ, Hare SR, Zhang Y, Wallace JM, Francis RC (1997) A pacific interdecadal climate oscillation with impacts on salmon production. Bull Am Meteorol Soc 78:1069–1079
Marchetti MP, Moyle PB (2001) Effects of flow regime on fish assemblages in a regulated California stream. Ecol Appl 11:530–539
Marchetti MP, Moyle PB, Levine R (2004) Alien fishes in California watersheds: characteristics of successful and failed invaders. Ecol Appl 14:587–596
McCullough DA (1999) A review and synthesis of effects of alterations to the water temperature regime on freshwater life stages of salmonids, with special reference to Chinook salmon. US EPA, Seattle
McCusker MR, Parkinson E, Taylor EB (2000) Mitochondrial DNA variation in rainbow trout (Oncorhynchus mykiss) across its native range: testing biogeographical hypotheses and their relevance to conservation. Mol Ecol 9:2089–2108
McGowan JA, Cayan DR, Dorman LM (1998) Climate-ocean variability and ecosystem response in the Northeast Pacific. Science 281:210–217
Mohseni O, Stefan HG, Eaton JG (2003) Global warming and potential changes in fish habitat in U.S. streams. Clim Chang 59:389– 409
Montgomery DR (2003) King of fish: the thousand-year run of salmon. Westview Press
Mote PW, Hamlet AF, Clark MP, Lettenmaier DP (2005) Declining mountain snowpack in western North America. Bull Am Meteorol Soc 86:39–49
Mote PW, Parson EA, Hamlet AF, Keeton WS, Lettenmaier D, Mantua N, Miles EL, Peterson DW, Peterson DL, Slaughter R, Snover AK (2003) Preparing for climatic change: the water, salmon, and forests of the Pacific Northwest. Clim Chang 59:389–409
Moyle PB (1969) Comparative behavior of young brook trout of domestic and wild origin. Prog Fish-Cult 31:51–56
Moyle PB (2002) Inland fishes of California. Regents of the University of California, Berkeley, p 502
Moyle PB, Marchetti MP (2006) Predicting invasion success: freshwater fishes in California as model. BioSci 56:515–524
Moyle PB, Purdy SE, Israel JA (2008) Salmon, steelhead, and trout in California: status of an emblematic fauna. California Trout, San Francisco, p 316
Moyle PB, Katz JVE, Quiñones RM (2011) Rapid decline of California’s native inland fishes: a status assessment. Biol Cons 144:2414–2423
Moyle PB, Quiñones RM, Katz JVE (in press) California fish species of special concern, 3rd edn. California Department of Fish and Game, Rancho Cordova
Mueter FJ, Peterman RM, Pyper BJ (2002) Opposite effects of ocean temperature on survival rates of 120 stocks of Pacific salmon (Oncorhynchus spp.) in northern and southern areas. Can J Fish Aquat Sci 59:456–463
Naish KA, Hard JJ (2008) Bridging the gap between the genotype and the phenotype: linking genetic variation, selection and adaptation in fishes. Fish Fish 9:396–422
National Marine Fisheries Service (2010) Public draft recovery plan for central California coast Coho Salmon (Oncorhynchus kisutch) Evolutionarily Significant Unit. National Marine Fisheries Service, Southwest Region, Santa Rosa, California
Nickelson T (2003) The influence of hatchery coho salmon (Oncorhynchus kisutch) on the productivity of wild coho salmon populations in Oregon coastal basins. Can J Fish Aquat Sci 60:1050–1056
Nickelson TE, Solazzi MF, Johnson SL (1986) Use of hatchery coho salmon (Oncorhynchus kisutch) presmolts to rebuild wild populations in Oregon coastal streams. Can J Fish Aquat Sci 43:2443–2449
Nielsen EE, Hansen MM, Loeschcke V (1999) Genetic variation in time and space: microsatellite analysis of extinct and extant populations of Atlantic salmon. Evolution 53:261–268
Noss RF, Franklin JF, Baker WL, Schoennagel T, Moyle PB (2006) Managing fire-prone forests in the western United States. Front Ecol Environ 9:481–487
Pearsons TN, Temple GM (2010) Changes to rainbow trout abundance and salmonid biomass in a Washington watershed as related to hatchery salmon supplementation. Trans Am Fish Soc 139:502–520
Pierce DW (2004) Future changes in biological activity in the North Pacific Due to anthropogenic forcing of the physical environment. Clim Chang 62:389–418
Quiñones RM, Moyle PB (in press) Integrating global climate change into salmon and trout conservation: a case study of the Klamath River. In: Root TL, Hall KR, Herzog M, Howell CA (eds) Linking science and management to conserve biodiversity in a changing climate. University of California Press, Berkeley
Reisenbichler RR, Rubin SP (1999) Genetic changes from artificial propagation of Pacific salmon affect the productivity and variability of supplemented populations. ICES J Mar Sci 56:459–466
Reusch TBH, Ehlers A, Hämmerli A, Worm B (2005) Ecosystem recovery after climatic extremes enhanced by genotypic diversity. Proc Natl Acad Sci USA 102:2826
Richter A, Kolmes S (2005) Maximum temperature limits for Chinook, coho, and chum salmon, and steelhead trout in the Pacific Northwest. Rev Fish Sci 13:23–49
Roessig JM, Woodley CM, Cech JJ, Hansen LJ (2004) Effects of global climate change on marine and estuarine fishes and fisheries. Rev Fish Biol Fish 14:251–275
Rogers LA, Schindler DE (2008) Asynchrony in population dynamics of sockeye salmon in southwestern Alaska. Oikos 117:1578–1586
Scavia D, Field J, Boesch D, Buddemeier R, Burkett V, Cayan D, Fogarty M, Harwell M, Howarth R, Mason C, Reed D, Royer T, Sallenger A, Titus J (2002) Climate change impacts on U.S. coastal and marine ecosystems. Estuar Coast 25:149–164
Scheuerell MD, Williams JG (2005) Forecasting climate-induced changes in the survival of Snake River spring/summer Chinook salmon (Oncorhynchus tshawytscha). Fish Ocean 14:448–457
Schindler DE, Augerot X, Fleishman E, Mantua NJ, Riddell B, Ruckelshaus M, Seeb J, Webster M (2008) Climate change, ecosystem impacts, and management for Pacific salmon. Fisheries 33:502–506
Schwing FB, Mendelssohn R, Bograd SJ, Overland JE, Wang M, Ito S (2010) Climate change, teleconnection patterns, and regional processes forcing marine populations in the Pacific. J Mar Syst 79:245–257
Stewart IT, Cayan DR, Dettinger MD (2004) Changes in snowmelt runoff timing in Western North America under a ‘business as usual’ climate change scenario. Clim Chang 62:217–232
Stewart IT, Cayan DR, Dettinger MD (2005) Changes toward earlier streamflow timing across Western North America. J Clim 18:1136–1155
Unwin MJ, Glova GJ (1997) Changes in life history parameters in a naturally spawning population of Chinook salmon (Oncorhynchus tshawytscha) associated with releases of hatchery-reared fish. Can J Fish Aquat Sci 54:1235–1245
Sugihara NG, Van Wagtendong JW, Shaffer KE, Fites-Kaulfman J, Thode AE (eds) (2006) Fire in California’s ecosystems. University of California Press, Berkeley
VanDevelder P (2011) A fish tale in the Land of Oz. High Country News, Paoinia
Wang M, Overland JE, Bond NA (2010) Climate projections for selected large marine ecosystems. J Mar Syst 79:258–266
Waples RS, Pess GR, Beechie T (2008) Evolutionary history of Pacific salmon in dynamic environments. Evol Appl 1:189–206
Waples RS, Beechie T, Pess GR (2009) Evolutionary history, habitat disturbance regimes, and anthropogenic changes: what do these mean for resilience of Pacific salmon populations? Ecol Soc 14:3
Wells BK, Grimes CB, Sneva JG, McPherson S, Waldvogel JB (2008) Relationships between oceanic conditions and growth of Chinook salmon (Oncorhynchus tshawytscha) from California, Washington, and Alaska, USA. Fish Ocean 17:101–125
Williams JG (2006) Central Valley salmon: a perspective on Chinook and steelhead in the Central Valley of California. San Francisco Estuary and Watershed Science 4
Williamson K, May B (2005) Homogenization of fall-run chinook salmon gene pools in the central valley of California, USA. N Am J Fish Manag 25:993–1009
Yoshiyama RM, Fisher FW, Moyle PB (1998) Historical abundance and decline of Chinook salmon in the Central Valley Region of California. N Am J Fish Manag 18:487–521
Yoshiyama RM, Moyle PB, Gerstung ER, Fisher FW (2000) Chinook salmon in the California Central Valley: an assessment. Fisheries 25:6–20
Acknowledgements
Initial funding for this project was provided by California Trout, Inc, through the Sage Fund. Funding for this analysis was provided by the California Department of Fish and Game and by the David and Lucile Packard Foundation, the Stephen Bechtel Fund, and the Resources Legacy Fund as part of the Delta Solutions program at UC Davis. This analysis would not have been possible without information and review provided willingly by dozens of biologists statewide, making this a true community effort. The views expressed are those of the authors and do not reflect official opinion of any institution.
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Appendices
Appendix A
Descriptions of factors causing decline used in Anthropogenic Threats Analysis
Major dams
Dams were recorded as having a high impact on a species if they cut off a species from a large amount of its range, if they caused major changes to habitat, or if they significantly changed water quality and quantity downstream of the dam. The effects of the reservoirs created by dams were also evaluated. Dams were regarded as having a low impact if they were present within the range of the species but their effects were either very small or poorly known.
Agriculture
The effects of agriculture were regarded as being high if agricultural return water or farm effluent heavily polluted streams, if diversions severely reduced flow, if large amounts of silt flowed into streams from farmland, if pesticides had significant impacts or were suspected of having them, and if other factors directly affected the streams in which a species lived. Agriculture was regarded as having a low impact if it was not pervasive in the watersheds in which the species lived or was not causing significant changes to aquatic environments.
Grazing
Livestock grazing was separated from other forms of agriculture because its effects are widespread on range and forest lands throughout California, especially the effects of cattle. Impacts are high where stream banks are trampled and riparian vegetation removed, resulting in streams becoming incised and the drying of adjacent wetlands. Removal of vegetation can also result in large amounts of silt being washed into streams, increased summer temperatures, and decreased summer flows. Impacts are low where grazing occurs in watersheds but changes described above are minimal.
Rural residential
As California’s human population grows, people spread across the landscape, often settling in diffuse patterns along or near streams. This results in water removal, streambed alteration (to protect houses, create swimming holes, construct road crossings, etc.), and pollution (especially from septic tanks). Where such housing is abundant and unregulated, it causes major changes to streams and their fishes and is rated as a high impact. Where such housing is present but scarce, the effects are usually low.
Urbanization
When humans concentrate in towns and cities, they alter the streams that flow through them to reduce flooding and acquire the water. Pollution is rampant, both through sewage discharges and through less obvious means such as storm drains. Generally, the bigger the city, the bigger its effects on local streams and fish populations.
Instream mining
The most severe instream mining took place during the 19th and early 20th century when miners excavated and dredged river beds for gold, turning them over multiple times. These severe legacy effects are still with us in many rivers. Nearly as severe, at least locally, have been instream gravel mining operations, in which large pits were dug into streambeds and banks altered. Such mining is largely banned (in favor of mining off-channel areas) but also has legacy effects. This was usually rated intermediate when present, although severe legacy affects resulted in high ratings for some species. The impacts of contemporary recreational and professional suction dredge mining for gold can also result in a high rating.
Mining
This refers to hard rock mining, in which tailings can be dumped into streams and pollutants result from mine drainage, mostly of abandoned mines. The effects of mercury, used in processing gold in placer and dredge mining is also included here. High ratings come from situation where mines, even if abandoned, form a major threat because their wastes are poised on the edges of rivers (e.g. Iron Mountain Mine near Redding). Low ratings for species usually come from situations where old mines are present but their effects on nearby streams are not known or not obvious.
Transportation
Historically, river banks were favorite places to construct roads and railroads, so many rivers and creeks have roads and railroads running along one or both sides, often confining the stream channel and subjecting the streams to pollution from vehicle emissions, waste disposal, and accidents. Also culverts and other drainage modifications associated with roads often block fish migration or restrict fish movements. Dirt roads can become hydrologically connected to streams, increasing siltation and changing local flow regimes and seriously impacting aquatic habitat. The ratings were made based on how pervasive roadside streams are in the areas occupied by the species
Logging
Timber harvest has always been one of the major uses of forested watersheds in California. These same watersheds support the most species and highest abundances of fish, including anadromous salmon and steelhead. Logging was relatively unregulated until the mid-20th century, resulting in major degradation of streams through removal of trees as cover and landscape stabilizers. Legacy effects include incised streams with little large wood providing structure and many silt-bottomed reaches. Logging is still a pervasive activity in forested watersheds and is better regulated today than previously, but its effects can still result in siltation of streams, reduced complexity of habitat, and other alterations. High ratings were given when a species occupied streams degraded by either the legacy or contemporary effects of logging. Low ratings were awarded to species that used forested watersheds but where the effects of logging were either mitigated or of small significance.
Fire
Forest, range, and scrub fires are part of California’s natural landscape but human activities have made them more severe (Gresswell 1999; Noss et al. 2006; Sugihara et al. 2006). Transition from relatively frequent understory fires to less frequent but catastrophic crown fires has been shown to be a major driver in the extinction risk of Gila trout (Oncorhynchus gilae) in New Mexico (Brown et al. 2001). There is little reason to think that similar factors are not pervasive in California. A fish species rated high for fire is one in which most of its streams are affected by fire, through increased erosion, increases in temperature, spills of fire-fighting chemicals, and effects of ash and other materials. Low ratings generally applied to fish that lived in areas where fires occur but for various reasons have minimal impact on streams.
Estuary alteration
Many California fishes depend on estuaries for at least part of their life cycle. All estuaries in the state are highly altered by human activity, from siltation to pollution, to diking and draining, to removal of sandbars between the estuary and ocean. Thus the more estuarine dependant a fish species is, the more likely it was to get a high rating for this factor.
Recreation
Human use of streams as playgrounds has greatly increased along with the human population but the effects are usually minor, although concentrated at periods of time when stream flows are low. Recreation is likely to be rated high as a factor when there is, for example, heavy off-road vehicle use in limited habitat, ski resorts that increase sedimentation (from cleared areas for ski runs), or rafters and swimmers disturbing spawning or holding fish (salmon and steelhead).
Harvest
Harvest of fishes is both legal and illegal. Both can have severe impacts on fish populations, especially of large fishes or ones that are isolated and therefore easy to catch (e.g. summer steelhead).
Hatcheries
Most fishes do not have populations supported in part by fish hatcheries but for those that do, hatcheries often have negative effects on wild populations through competition for space and food, direct predation, and loss of fitness and genetic diversity (Kostow 2009; Chilcote et al. 2011). The severity of these effects was rated based in part on hatchery dependence and/or the threat of interbreeding between wild and hatchery populations.
Alien species
Non-native species are present in every California watershed and their impacts on native species through hybridization, predation, competition, and disease are often severe (Moyle and Marchetti 2006). Fish species were rated high in this category if there were studies demonstrating major direct or indirect impacts of alien invaders. They were rated low if contact with aliens was frequent but not negative.
Appendix B
Appendix C
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Katz, J., Moyle, P.B., Quiñones, R.M. et al. Impending extinction of salmon, steelhead, and trout (Salmonidae) in California. Environ Biol Fish 96, 1169–1186 (2013). https://doi.org/10.1007/s10641-012-9974-8
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DOI: https://doi.org/10.1007/s10641-012-9974-8