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Research about Klamath River Basin

Source-linked reports with geographic coverage including Klamath River Basin.

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Water and endangered fish in the Klamath River Basin: Do Upper Klamath Lake surface elevation and water quality affect adult Lost River and Shortnose Sucker survival?

In the western United States, water allocation decisions often incorporate the needs of endangered fish. In the Klamath River basin, an understanding of temporal variation in annual survival rates of Shortnose Suckers Chasmistes brevirostris and Lost River Suckers Deltistes luxatus and their relation to environmental drivers is critical to water management and sucker recovery. Extinction risk is high for these fish because most individuals in the populations are approaching their maximum life span and recruitment of new fish into the adult populations has never exceeded mortality losses in the past 22 years. We used a time series of mark–recapture data from the years 1999–2021 to analyze the relationship between lake level, water quality covariates, and survival of adult Shortnose Suckers and two spawning populations of Lost River Suckers in Upper Klamath Lake, Oregon. We compared competing model hypotheses in a maximum likelihood framework using Akaike's information criterion and then ran the top environmental covariates in a Bayesian framework to estimate how much of the variation in survival was explained by these covariates as compared to random variation. The complementary analyses found almost unequivocal support for our base model without environmental covariates. Estimated adult sucker survival was high across the time series and consistent with sucker life history (mean annual survival = 0.82–0.91). This suggests that adult suckers were generally robust to interannual variation in lake levels as well as consistently poor water quality within the years of our data set. Recovery time is limited, as a declining survival trend for adult suckers in recent years may be due to the onset of senescence. The successful recovery of suckers in Upper Klamath Lake may rely on shifting research from the causes of adult mortality and its relationship with lake surface elevation to the causes of poor recruitment into adult populations.

California, Oregon

Characterization of the genetic structure of four sucker species in the Klamath River. Final Report

Four species of suckers (family Catostomidae) inhabit the Klamath River Basin of Oregon and California: Lost River suckers (LRS; Deltistes luxatus), shortnose suckers (SNS; Chasmistes brevirostris), Klamath largescale suckers (KLS; Catostomus snyderi), and Klamath smallscale suckers (KSS; Catostomus rimiculus). All but Klamath smallscale suckers are endemic and restricted to the Klamath River Basin where they occur sympatrically in large lakes and reservoirs, including the Lost River and Klamath Lake subbasins (Figure 1; USFWS 2012). Population declines, primarily due to loss or degradation of spawning, rearing, and adult habitat, have resulted in Lost River and shortnose suckers being listed as endangered throughout their entire range under the U.S. Endangered Species Act (USFWS 1988). Continued population declines coupled with failed adult recruitment prompted the USFWS to initiate an assisted rearing program in 2015 as a part of their recovery strategy (Childress et al. 2019). The program was designed to maintain as much genetic diversity as possible while improving recruitment by averting high early life stage mortality (Day et al. 2017). However, while assisted rearing efforts are targeted towards endangered LRS and SNS, species differentiation of larval and juvenile suckers is problematic in the Klamath River Basin. This, in turn, complicates the management of these species as well as the population modeling used to evaluate recovery efforts. Maintaining as much as possible of the genetic resources, or “evolutionary legacy” of a species is a goal common to conservation and endangered species recovery strategies. Inappropriate assumptions regarding species’ evolutionary lineages, and genetic characteristics may lead to the mismanagement of an endangered species through a failure to recognize and appropriately manage species boundaries and genetic population structure. Despite a considerable amount of research, the partitioning of genetic diversity within and among the four species of suckers in the Klamath River Basin remains unclear. Previously developed genetic markers are effective at differentiating some species, but fail to effectively differentiate all four species of suckers in the basin (Tranah et al. 2001; Wagman 2003; Tranah and May 2006; Hoy and Ostberg 2015; Dowling et al. 2016). Peer-reviewed publications describing the morphological characteristics of (Markle et al. 2005) and genetic relationships among (Dowling et al. 2016; Tranah and May 2006) Klamath River Basin suckers have not resolved uncertainties regarding the systematic relationships among the four currently recognized taxa. Specifically, genetic and morphological data generally support LRS and KSS as being distinct entities, but genetic evidence does not support a distinction between KLS and SNS. All three publications above refer to unpublished information regarding ecological differences between KLS and SNS as evidence to support the existence of two entities. However, the authors also acknowledge that overlap in morphological characters (Markle et al. 2005) and a lack of genetic differentiation (Dowling et al. 2016; Tranah and May 2006) between KLS and SNS raises the question of their specific identity. This is particularly problematic in the Lost River subbasin, where overlap in morphological characters between KLS and SNS is greatest. In our opinion, the basis of the strong genetic similarity between KLS and SNS has not been resolved. Morphological characters mostly support the existence of two distinct species, while genetic characters do not (i.e., genetic divergence between KLS and SNS is less than divergence among populations of each species; (Smith et al. 2015). Some have suggested that introgressive hybridization may have resulted in a lack of genetic differentiation between KLS and SNS and a breakdown of monophyletic species (Dowling et al. 2016; Tranah and May 2006), and that this hybridization may be an important process in

California, Oregon

Evolutionary dynamics of Ceratonova species (Cnidaria: Myxozoa) reveal different host adaptation strategies

The myxozoan parasite Ceratonova shasta is an important pathogen that infects multiple species of Pacific salmonids. Ongoing genetic surveillance has revealed stable host-parasite relationships throughout the parasite's endemic range. We applied Bayesian phylogenetics to test specific hypotheses about the evolution of these host-parasite relationships within the well-studied Klamath River watershed in Oregon and California, USA. The results provide statistical support that different genotypes of C. shasta are distinct lineages of one species, which is related to two other Ceratonova species in the same ecosystems; Ceratonova X in speckled dace and C. gasterostea in threespine stickleback. Furthermore, we found strong support for the hypothesis that C. shasta type 0 in native steelhead trout and type I in Chinook salmon each evolved with a specialist host adaptation strategy, while C. shasta type II in coho salmon resulted from a generalist host adaptation strategy. Inferred date and host species of the most recent common ancestor of extant Klamath basin types indicate that it occurred between 14,000 and 21,000 years ago, and most likely infected a native steelhead or rainbow trout host.

California, Oregon

Klamath River Basin water-quality data

The Klamath River Basin stretches from the mountains and inland basins of south-central Oregon and northern California to the Pacific Ocean, spanning multiple climatic regions and encompassing a variety of ecosystems. Water quantity and water quality are important topics in the basin, because water is a critical resource for farming and municipal use, power generation, and for the support of wildlife, aquatic ecosystems, and endangered species. Upper Klamath Lake is the largest freshwater lake in Oregon (112 square miles) and is known for its seasonal algal blooms. The Klamath River has dams for hydropower and the upper basin requires irrigation water to support agriculture and grazing. Multiple species of endangered fish inhabit the rivers and lakes, and the marshes are key stops on the Pacific flyway for migrating birds. For these and other reasons, the water resources in this basin have been studied and monitored to support their management distribution.

California, Oregon

Life history diversity in Klamath River steelhead

Oncorhynchus mykiss exhibits a vast array of life histories, which increases its likelihood of persistence by spreading risk of extirpation among different pathways. The Klamath River basin (California–Oregon) provides a particularly interesting backdrop for the study of life history diversity in O. mykiss , in part because the river is slated for a historic and potentially influential dam removal and habitat recolonization project. We used scale and otolith strontium isotope ( 87 Sr/ 86 Sr) analyses to characterize life history diversity in wild O. mykiss from the lower Klamath River basin. We also determined maternal origin (anadromous or nonanadromous) and migratory history (anadromous or nonanadromous) of O. mykiss and compared length and fecundity at age between anadromous (steelhead) and nonanadromous (Rainbow Trout) phenotypes of O. mykiss . We identified a total of 38 life history categories at maturity, which differed in duration of freshwater and ocean rearing, age at maturation, and incidence of repeat spawning. Approximately 10% of adult fish sampled were nonanadromous. Rainbow Trout generally grew faster in freshwater than juvenile steelhead; however, ocean growth afforded adult steelhead greater length and fecundity than adult Rainbow Trout. Although 75% of individuals followed the migratory path of their mother, steelhead produced nonanadromous progeny and Rainbow Trout produced anadromous progeny. Overall, we observed a highly diverse array of life histories among Klamath River O. mykiss . While this diversity should increase population resilience, recent declines in the abundance of Klamath River steelhead suggest that life history diversity alone is not sufficient to stabilize a population. Our finding that steelhead and Rainbow Trout give rise to progeny of the alternate form (1) suggests that dam removal might lead to a facultatively anadromous O. mykiss population in the upper basin and (2) raises the question of whether both forms of O. mykiss in the Klamath River should be managed under the same strategy.

California, Oregon

Demographics and run timing of adult Lost River ( Deltistes luxatus ) and shortnose ( Chasmistes brevirostris ) suckers in Upper Klamath Lake, Oregon, 2011

Executive Summary Data from a long-term capture-recapture program were used to assess the status and dynamics of populations of two long-lived, federally endangered catostomids in Upper Klamath Lake, Oregon. Lost River suckers ( Deltistes luxatus ) and shortnose suckers ( Chasmistes brevirostris ) have been captured and tagged with passive integrated transponder (PIT) tags during their spawning migrations in each year since 1995. In addition, beginning in 2005, individuals that had been previously PIT-tagged were re-encountered on remote underwater antennas deployed throughout sucker spawning areas. Captures and remote encounters during spring 2011 were used to describe the spawning migrations in that year and also were incorporated into capture-recapture analyses of population dynamics. Cormack-Jolly-Seber (CJS) open population capture-recapture models were used to estimate annual survival probabilities, and a reverse-time analog of the CJS model was used to estimate recruitment of new individuals into the spawning populations. In addition, data on the size composition of captured fish was examined to provide corroborating evidence of recruitment. Survival and recruitment estimates were used to derive estimates of changes in population size over time and to determine the status of the populations in 2010. Separate analyses were conducted for each species and also for each subpopulation of Lost River suckers (LRS). One subpopulation of LRS migrates into tributaries to spawn, similar to shortnose suckers (SNS), whereas the other subpopulation spawns at upwelling areas along the eastern shoreline of the lake. In 2011, we captured, tagged, and released 806 LRS at four lakeshore spawning areas and recaptured an additional 1,006 individuals that had been tagged in previous years. Across all four areas, the remote antennas detected 6,547 individual LRS during the spawning season. Spawning activity peaked in April and most individuals were encountered at Sucker Springs and Cinder Flats. In the Williamson River, we captured, tagged, and released 2,742 LRS and 123 SNS, and recaptured 376 LRS and 58 SNS that had been tagged in previous years. Remote PIT tag antennas in the traps at the weir on the Williamson River and remote antenna systems that spanned the river at four different locations on the Williamson and Sprague Rivers detected a total of 16,494 LRS and 5,450 SNS. Most LRS passed upstream between mid-April and mid-May when water temperatures were rising and near or greater than 10 °C. In contrast, the largest peaks in upstream passage of SNS occurred in early and mid-May when water temperatures were rising and near or greater than 12 °C. Finally, an additional 875 LRS and 1,600 SNS were captured in trammel net sampling at pre-spawn staging areas in the northeastern portion of the lake. Of these, 191of the LRS and 571 of the SNS had been PIT-tagged in previous years. For LRS, encounter histories showed that more than 90 percent of the fish captured at the staging areas were members of the subpopulation that spawns in the tributaries. Capture-recapture analyses for the LRS subpopulation that spawns at the shoreline areas included encounter histories for more than 10,500 individuals, and analyses for the subpopulation that spawns in the tributaries included more than 22,000 encounter histories. With a few exceptions, the survival of males and females in both subpopulations was high (greater than 0.9) between 1999 and 2009. Notably lower survival occurred for both sexes from the tributaries in 2000, for both sexes from the shoreline areas in 2002, and for males from the tributaries in 2006. Between 2001 and 2010, the abundance of males in the lakeshore spawning subpopulation decreased by 50–60 percent and the abundance of females decreased by 29–44 percent. Capture-recapture models suggested that the abundance of the river spawning subpopulation of LRS has increased substantially since 2006. The increase over this period was largely due to large estimated recruitment events in 2003, 2006, and 2008. We know that the estimate in 2006 is substantially biased in favor of recruitment due to a sampling issue. We are skeptical of the magnitude of recruitment indicated by the 2003 and 2008 estimates as well because very few small individuals that would indicate the presence of new recruits were captured in those years. If we assume that little or no recruitment has occurred, the abundance of both sexes in the river spawning subpopulation decreased by more than 40 percent between 2002 and 2010. Capture-recapture analyses for SNS included encounter histories for more than 15,500 individuals. The majority of annual survival estimates between 2001 and 2009 were high (greater than 0.8), but SNS did experience more years of low survival than either LRS subpopulation. The survival of both sexes was particularly low in both 2001 and 2004, and male survival also was somewhat low in 2002 and 2006. Capture-recapture models and size composition data indicated that recruitment of new individuals into the SNS spawning population was trivial in nearly all years between 2001 and 2009. As a result, the abundance of males decreased by 64–82 percent and the abundance of females decreased by 62–76 percent between 2001 and 2010. Despite relatively high survival in most years, both species have experienced substantial declines in the abundance of spawning fish because losses from mortality have not been balanced by recruitment of new individuals. Although capture-recapture data indicate substantial recruitment of new individuals into the adult spawning populations for SNS and river spawning LRS in some years, size data do not corroborate these estimates. In fact, fork length data indicate that all populations are largely comprised of fish that were present in the late 1990s and early 2000s. As a result, the status of the endangered sucker populations in Upper Klamath Lake remains worrisome, and the situation is most dire for shortnose suckers. Future investigations should explore the connections between sucker recruitment and survival and various environmental factors, such as water quality and disease. Our monitoring program provides a robust platform for estimating vital population parameters, evaluating the status of the populations, and assessing the effectiveness of conservation and recovery efforts.

California, Oregon

Estimation of stream temperature in support of fish production modeling under future climates in the Klamath River Basin

Stream temperature estimates under future climatic conditions were needed in support of fish production modeling for evaluation of effects of dam removal in the Klamath River Basin. To allow for the persistence of the Klamath River salmon fishery, an upcoming Secretarial Determination in 2012 will review potential changes in water quality and stream temperature to assess alternative scenarios, including dam removal. Daily stream temperature models were developed by using a regression model approach with simulated net solar radiation, vapor density deficit calculated on the basis of air temperature, and mean daily air temperature. Models were calibrated for 6 streams in the Lower, and 18 streams in the Upper, Klamath Basin by using measured stream temperatures for 1999-2008. The standard error of the y-estimate for the estimation of stream temperature for the 24 streams ranged from 0.36 to 1.64°C, with an average error of 1.12°C for all streams. The regression models were then used with projected air temperatures to estimate future stream temperatures for 2010-99. Although the mean change from the baseline historical period of 1950-99 to the projected future period of 2070-99 is only 1.2°C, it ranges from 3.4°C for the Shasta River to no change for Fall Creek and Trout Creek. Variability is also evident in the future with a mean change in temperature for all streams from the baseline period to the projected period of 2070-99 of only 1°C, while the range in stream temperature change is from 0 to 2.1°C. The baseline period, 1950-99, to which the air temperature projections were corrected, established the starting point for the projected changes in air temperature. The average measured daily air temperature for the calibration period 1999-2008, however, was found to be as much as 2.3°C higher than baseline for some rivers, indicating that warming conditions have already occurred in many areas of the Klamath River Basin, and that the stream temperature projections for the 21st century could be underestimating the actual change.

Oregon;California

Water quality modeling in the systems impact assessment model for the Klamath River basin - Keno, Oregon to Seiad Valley, California

This report describes the water quality model developed for the Klamath River System Impact Assessment Model (SIAM). The Klamath River SIAM is a decision support system developed by the authors and other US Geological Survey (USGS), Midcontinent Ecological Science Center staff to study the effects of basin-wide water management decisions on anadromous fish in the Klamath River. The Army Corps of Engineersa?? HEC5Q water quality modeling software was used to simulate water temperature, dissolved oxygen and conductivity in 100 miles of the Klamath River Basin in Oregon and California. The water quality model simulated three reservoirs and the mainstem Klamath River influenced by the Shasta and Scott River tributaries. Model development, calibration and two validation exercises are described as well as the integration of the water quality model into the SIAM decision support system software. Within SIAM, data are exchanged between the water quantity model (MODSIM), the water quality model (HEC5Q), the salmon population model (SALMOD) and methods for evaluating ecosystem health. The overall predictive ability of the water quality model is described in the context of calibration and validation error statistics. Applications of SIAM and the water quality model are described.

California, Oregon

Modeling and management of water in the Klamath River Basin: overcoming politics and conflicts

The network flow model MODSIM, which was designed as a water quantity mass balance model for evaluating and selecting water management alternatives, has been applied to the Klamath River basin. A background of conflicting issues in the basin is presented. The complexity of water quantity model development, while satisfying the many stakeholders and involved special interest groups is discussed, as well as the efforts taken to have the technical model accepted and used, and overcome stakeholder criticism, skepticism, and mistrust of the government.

Oregon