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Temporal and spatial distribution of endangered juvenile Lost River and shortnose suckers in relation to environmental variables in Upper Klamath Lake, Oregon: 2009 annual data summary

Lost River sucker (Deltistes luxatus) and shortnose sucker (Chasmistes brevirostris) were listed as endangered in 1988 for a variety of reasons including apparent recruitment failure. Upper Klamath Lake, Oregon, and its tributaries are considered the most critical remaining habitat for these two species. Age-0 suckers are often abundant in Upper Klamath Lake throughout the summer months, but catches decline dramatically between late August and early September each year. Similar declines of age-1 suckers between spring and late summer also occur annually. These rapid declines in catch rates and a lack of substantial recruitment into adult sucker populations in recent years suggests sucker populations experience high mortality between their first summer and first spawn. Summer age-0 sucker habitat use and distribution have been studied extensively, but many uncertainties remain about age-1 and older juvenile habitat use, distribution, and movement patterns within Upper Klamath Lake. This study was designed to examine seasonal changes in distribution of age-1 suckers in Upper Klamath Lake as they relate to depth and water quality. The results of our third annual spring and summer sampling effort are presented in this report. Catch data collected in 2009 indicate seasonal changes in age-1 and older juvenile sucker habitat use coincident with changes in water quality. Although age-1 sucker catch rates were again concentrated along the western shore in June and early July, as they were in 2007 and 2008, very few age-1 suckers were captured in Eagle Ridge Trench in 2009 - a deepwater area along the western shore extending from Howard Bay to Eagle Ridge Point. Instead, suckers in 2009 were concentrated in the relatively shallow bays along the western shore. Nevertheless, as dissolved-oxygen concentrations decreased in mid-July below sublethal thresholds around the Eagle Ridge Trench, age-1 suckers apparently moved away from the western shore, and subsequently were captured in main lake areas and the eastern shore. Age-1 suckers were noticeably absent from the tributaries of Upper Klamath Lake during periods of chronically low dissolved-oxygen concentrations in the lake, refuting a previously untested hypothesis that tributaries were important age-1 sucker refuge habitats. In addition, declines in overall catch rates for age-1 suckers in August and September, despite intensive sampling, indicates that the apparent declines in abundance may be due to increased mortality and not due to sampling the wrong environments or poor detection probability. The remote detection of an age-1 juvenile sucker tagged in Short Creek and subsequently recaptured in the Link River array, more than 30 kilometers away, indicates the capacity of juvenile suckers to migrate relatively long distances. This knowledge, coupled with other remotely detected suckers in the Williamson River, indicates that juvenile sucker movement in Upper Klamath Lake may be common. In order to better quantify movement and potentially survival, future research should focus on tagging more juvenile suckers and taking advantage of the significant passive integrated transponder tag infrastructure throughout Upper Klamath Lake and its tributaries. In this data summary, we also describe the distribution of age-0 suckers in Upper Klamath Lake and its tributaries. These data corroborate findings from 2007 and 2008, which describe age-0 sucker habitat as shallow relative to depths available in Upper Klamath Lake. Similar to age-1 suckers, age-0 sucker abundances also appeared to decline in late summer, despite continued sampling throughout Upper Klamath Lake and its tributaries. In addition to low dissolved-oxygen concentrations, increased opercle deformity and anchor worm (Lernaea spp.) infection rates, as well as increased abundances of fathead minnows and other piscivorous non-native fish, may provide potential insight into the causes of juvenile sucker rarity. Opercle deformity r

Open-File Report↗

Population ecology of variegate darter (Etheostoma variatum) in Virginia

Variegate darters ( Etheostoma variatum ) were listed as endangered in Virginia in 1992. Reasons for listing included habitat degradation and concerns about current and future impacts of coal mining throughout their Virginia range. Prior to this research, little was known about variegate darter distribution, habitat use, or populations in Virginia. Two primary goals of this research were to gain knowledge about the current population ecology and the relationship between landscape-level factors (e.g., land cover changes, watershed size, isolation from other populations) on current and past variegate darter population sizes. We investigated distribution, habitat suitability, population genetics, and population size and structure of variegate darters in the upper Big Sandy River drainage, Buchanan, Dickenson, and Wise Co., Virginia. Our results indicate variegate darters are primarily found in the Levisa Fork, with highest densities and abundances between its confluence with Dismal Creek and the Virginia-Kentucky border. Sporadic occurrences in smaller tributaries to the Levisa and Tug forks indicate they exist more widely in low densities, especially near the confluence with the Tug and Levisa mainstems. Detection of variegate darters in smaller tributaries was inconsistent, with reach-level occupancy estimates varying among years. We detected young-of-year variegate darters every year we sampled, but age 1 + darters were indistinguishable from older darters based on standard length. Variegate darter population size and stability in Virginia were estimated via multiple methods, including site occupancy surveys, mark-recapture studies, and population genetic analysis. Using mark-recapture methods at five sites, we estimated overall population size in 2011 to be approximately 12,800 individuals in the 35-km reach between the Levisa Fork - Dismal Creek confluence and the Virginia-Kentucky border. Age structure seemed stable, with breeding adults and young-of-year collected annually during 2008-2011. Population genetic analysis indicated variegate darters in the Levisa Fork and its tributaries are part of a single genetic population. Historical and current genetic stability were seen in our analysis of the variegate darter population, with no genetic differentiation among riffles across the upper Levisa Fork watershed, indicating dispersal among these sites is enough to overcome random genetic drift. This population is genetically isolated from downstream populations by the dam at Fishtrap Lake, Pike Co., Kentucky, and is beginning to show genetic isolation from other nearby populations. As expected, the Virginia population is most closely related to those in the Russell Fork and Levisa Fork downstream of the dam. Regular monitoring of variegate darters in the Levisa Fork mainstem from the Dismal Creek confluence to the Virginia-Kentucky border would facilitate better understanding of normal fluctuations of population size and distribution, as well as assessments of population status. This reach encompasses the core of the variegate darter population in Virginia, and its persistence will determine long-term viability of this species. Given that little is known about long-term population trends, we suggest that annual site-occupancy and population size estimates be made at ten randomly selected riffles for at least ten years to understand normal levels of variability. Thereafter, these population parameters could be monitored bi-annually as a way to detect shrinking distribution or abundance, especially after any fish kill or other pollution event in the Levisa Fork. We further suggest that the sites upstream and downstream of the saline diffusor pipe be monitored to detect changes in the extent of the impact zone. Overall, the variegate darter population in Virginia appears stable, although primarily confined to the lower 35 km of the Levisa Fork. Nevertheless, variegate darters in Virginia remain susceptible to extirpation due to catastrophic events, both physical (chemical spill) and biological (disease outbreak or invasive species introduction).

Virginia, West Virginia↗

Characterization of estuary use by Nisqually Hatchery Chinook based on Otolith analysis

INTRODUCTION The Nisqually Fall Chinook population is one of 27 stocks in the Puget Sound evolutionarily significant unit listed as threatened under the federal Endangered Species Act (ESA). Preservation and extensive restoration of the Nisqually delta ecosystem are planned to assist in recovery of the stock. A pre-restoration baseline including life history types, estuary residence time, growth rates, and habitat use are needed to evaluate the potential response of hatchery and wild Chinook salmon to restoration. Otolith analysis has been selected as a means to examine Chinook salmon life history, growth, and residence in the Nisqually estuary. Over time, the information from the otolith analyses will be used to: 1) determine if estuary restoration actions cause changes to the population structure (i.e. frequency of the different life history trajectories) for Nisqually River Chinook, 2) compare pre- and post- restoration residence times and growth rates, 3) suggest whether estuary restoration yields substantial benefits for Chinook salmon through (1) and (2), and 4) compare differences in habitat use between hatchery and wild Chinook to further protect ESA listed stock. Otoliths are calcium carbonate structures in the inner ear that grow in proportion to the overall growth of the fish. Daily growth increments can be measured so date and fish size at various habitat transitions can be back-calculated. Careful analysis of otolith microstructure can be used to determine the number of days that a fish resided in the estuary as a juvenile (increment counts), size at entrance to the estuary, size at egress, and the amount that the fish grew while in the estuary. Juvenile hatchery Chinook salmon are generally released as smolts that move quickly through the delta with much shorter residence times than for many wild fish and are not dependent on the delta as nursery habitat (Myers and Horton 1982; Mace 1983; Levings et al. 1986). The purpose of this study is to use and evaluate otolith microstructure analysis as a tool for assessing the role of the estuary in the life history of hatchery Chinook salmon in the Nisqually River before and after restoration efforts at the Nisqually National Wildlife Refuge (Nisqually NWR). This tool is used to quantify changes in rate of growth, length of residence and habitat use to help predict restoration benefits to the federally threatened Nisqually River hatchery and wild Chinook salmon populations. Analysis of otolith microstructure typically is superior to the alternative of traditional mark-recapture methods. The latter are extremely expensive or inadequate in estuary habitats, typically are biased and substantially underestimate use, and do not directly reveal the importance or contribution to adult recruitment (i.e., they do not account for any differential survival afterward in Puget Sound or the ocean). Analysis of otolith microstructure for these purposes is proving successful for the Nisqually wild Chinook stock as well as a similar study that USGS and partners are conducting in the Skagit River estuary system located in northern Puget Sound. This work is based on research by Neilson et al. (1985). We expect to use the Skagit River as a reference for the before/after restoration comparison in the Nisqually River.

Open-File Report↗

Gopherus agassizii (Cooper 1861) – Agassiz’s Desert Tortoise, Mojave Desert Tortoise

The Mojave Desert Tortoise, Gopherus agassizii (Family Testudinidae), is a large terrestrial species that can reach >370 mm in straight midline carapace length (CL) but most individuals are smaller. Both sexes reach adulthood at 12 to 21 years and ca. 180 mm CL. The species is sexually dimorphic, with males typically larger than females; sexual characteristics of males become more obvious with increasing size and age. Females lay from 1 to 10 eggs per clutch and from 0 to 3 clutches annually, with eggs hatching after 67 to 104 days. Populations of G. agassizii have declined rapidly over the last several decades. Habitat throughout the geographic range has experienced major losses, degradation, and fragmentation as a result of urban and agricultural development, livestock grazing, military activities, transportation and utility corridors, high levels of visitor use, vehicle-oriented recreation, and energy development. Disturbed habitats were vulnerable to invading non-native grasses and forbs, creating an unnatural and destructive grass-fire cycle. When consumed by tortoises as their only diet, non-native (and native) grasses are harmful because of limited nutrients. Additionally, subsidized predators (Common Ravens, Coyotes, and dogs), infectious diseases, drought, and vandalism, add to the catastrophic effects of habitat loss and degradation. Tortoise populations have declined rapidly in density, and most populations are below viability, with fewer than 3.9 adults/km2. These declines occurred despite protections afforded by federal and state laws and regulations, ca. 26,000 km2 of federally designated critical habitat units, two Recovery Plans, and efforts to reduce the negative impacts of human activities. As noted by Allison and McLuckie (2018), the negative population trends in most of the critical habitat units suggest that under current conditions G. agassizii is on the path to extinction. Distribution. – USA. Distributed in parts of the southern Great Basin, Mojave, and western Sonoran deserts in southeastern California, southern Nevada, northwestern Arizona, and southwestern Utah, north and west of the Grand Canyon/Colorado River complex, with the exception of a small population east of the Colorado River. Synonymy. – Xerobates agassizii Cooper 1861, Testudo agassizii, Gopherus agassizii, Gopherus polyphemus agassizii, Scaptochelys agassizii, Xerobates lepidocephalus Ottley and Velázques Solis 1989. Subspecies . – None currently recognized. Status. – IUCN 2019 Red List: Vulnerable (VU A1acde+2cde; assessed 1996) ; TFTSG Provisional Red List: Critically Endangered (CR; assessed 2011, 2018); CITES: Appendix II (Testudinidae spp.); US ESA: Threatened.

Arizona, California, Nevada, Utah↗

Southwestern Willow Flycatcher Breeding Site and Territory Summary - 2007

The Southwestern willow flycatcher (Empidonax traillii extimus; hereafter references to willow flycatcher and flycatcher refer to E.t. extimus, except where specifically noted) is an endangered bird that breeds only in dense riparian habitats in parts of six Southwestern states (Arizona, New Mexico, southern California, extreme southern Nevada, southern Utah, and southwestern Colorado). Since 1993, hundreds of Southwestern willow flycatcher surveys have been conducted each year, and many new flycatcher breeding sites located. This document synthesizes the most current information available on all known Southwestern willow flycatcher breeding sites. This rangewide data synthesis was designed to meet two objectives: (1) identify all known Southwestern willow flycatcher breeding sites and (2) assemble data to estimate population size, location, habitat, and other information for all breeding sites, for as many years as possible, from 1993 through 2007. This report provides data summaries in terms of the number of flycatcher sites and the number of territories. When interpreting and using this information, it must be kept in mind that a 'site' is a geographic location where one or more willow flycatchers establishes a territory. Sites with unpaired territorial males are considered breeding sites, even if no nesting attempts were documented. A site is often a discrete patch of riparian habitat but may also be a cluster of riparian patches; there is no standardized definition for site, and its use varies within and among states. For example, five occupied habitat patches along a 10-km stretch of river might be considered five different sites in one state but only a single site in another state. This lack of standardization makes comparisons based on site numbers problematic. Researchers for this report generally deferred to statewide summary documents or to local managers and researchers when delineating a site for inclusion in the database. However, to avoid inflating the number of sites and to establish more consistent definitions of the term 'site', adjacent and nearby sites from statewide reports were sometimes considered as a single site for the purposes of the rangewide data summary. Any combining or splitting of sites at the rangewide level was done on a case-by-case basis. Because of differences in site definitions, one should not evaluate the relative importance of a geographic region (such as drainage, watershed, or state) simply according to the number of flycatcher sites. A 'territory' is an exclusive defended area within a breeding site. Although detailed monitoring studies have identified unpaired territorial males and polygynous males at some flycatcher breeding sites, for the purposes of this report a territory is equivalent to the exclusive breeding area of a pair of flycatchers. In general, the concept of territory is more similar among states and different investigators than site; thus, it is a more robust unit to use for summaries and comparisons. However, note that the definition of a polygynous territory is not consistent among states; a male polygynously paired with two females would be considered one territory in some states and two territories in other states. For each site, we referred to reports or spoke directly with researchers and managers to gather information such as management entity/agency, location (state, drainage, elevation), gross habitat type (native, exotic, or mixed; dominant tree species), and number of flycatcher territories. Synthesizing the information on more than 200 breeding sites is challenging because annual data-collection and survey-reporting requirements are not standardized rangewide, and the nature and degree of readily available information varies widely from state to state. This is particularly true for areas such as California, where there are many flycatcher sites but surveyors are not required to submit standardized flycatcher survey forms. The lack of c

Open-File Report↗

Bathymetry of Walker Lake, West-Central Nevada

Walker Lake lies within a topographically closed basin in west-central Nevada and is the terminus of the Walker River. Much of the streamflow in the Walker River is diverted for irrigation, which has contributed to a decline in lake-surface altitude of about 150 feet and an increase in dissolved solids from 2,500 to 16,000 milligrams per liter in Walker Lake since 1882. The increase in salinity threatens the fresh-water ecosystem and survival of the Lahontan cutthroat trout, a species listed as threatened under the Endangered Species Act. Accurately determining the bathymetry and relations between lake-surface altitude, surface area, and storage volume are part of a study to improve the water budget for Walker Lake. This report describes the updated bathymetry of Walker Lake, a comparison of results from this study and a study by Rush in 1970, and an estimate of the 1882 lake-surface altitude. Bathymetry was measured using a single-beam echosounder coupled to a differentially-corrected global positioning system. Lake depth was subtracted from the lake-surface altitude to calculate the altitude of the lake bottom. A Lidar (light detection and ranging) survey and high resolution aerial imagery were used to create digital elevation models around Walker Lake. The altitude of the lake bottom and digital elevation models were merged together to create a single map showing land-surface altitude contours delineating areas that are currently or that were submerged by Walker Lake. Surface area and storage volume for lake-surface altitudes of 3,851.5-4,120 feet were calculated with 3-D surface-analysis software. Walker Lake is oval shaped with a north-south trending long axis. On June 28, 2005, the lake-surface altitude was 3,935.6 feet, maximum depth was 86.3 feet, and the surface area was 32,190 acres. The minimum altitude of the lake bottom from discrete point depths is 3,849.3 feet near the center of Walker Lake. The lake bottom is remarkably smooth except for mounds near the shore and river mouth that could be boulders, tree stumps, logs, or other submerged objects. The echosounder detected what appeared to be mounds in the deepest parts of Walker Lake, miles from the shore and river mouth. However, side-scan sonar and divers did not confirm the presence of mounds. Anomalies occur in two northwest trending groups in northern and southern Walker Lake. It is hypothesized that some anomalies indicate spring discharge along faults based on tufa-like rocks that were observed and the northwest trend parallel to and in proximity of mapped faults. Also, evaporation measured from Walker Lake is about 50 percent more than the previous estimate, indicating more water is flowing into the lake from sources other than the Walker River. Additional studies need to be done to determine what the anomalies are and whether they are related to the hydrology of Walker Lake. Most differences in surface area and storage volume between this study and a study by Rush in 1970 were less than 1 percent. The largest differences occur at lake-surface altitudes less than 3,916 feet. In general, relations between lake-surface altitude, surface area, and storage volume from Rush's study and this study are nearly identical throughout most of the range in lake-surface altitude. The lake-surface altitude in 1882 was estimated to be between 4,080 feet and 4,086 feet with a probable altitude of 4,082 feet. This estimate compares well with two previous estimates of 4,083 feet and 4,086 feet. Researchers believe the historic highstand of Walker Lake occurred in 1868 and estimated the highstand was between 4,089 feet and 4,108 feet. By 1882, Mason Valley was predominantly agricultural. The 7-26 feet decline in lake-surface altitude between 1868 and 1882 could partially be due to irrigation diversions during this time.

Scientific Investigations Report↗

The potential influence of changing climate on the persistence of salmonids of the inland west

The Earth's climate warmed steadily during the 20th century, and mean annual air temperatures are estimated to have increased by 0.6°C (Intergovernmental Panel on Climate Change, 2007). Although many cycles of warming and cooling have occurred in the past, the most recent warming period is unique in its rate and magnitude of change (Siegenthaler and others, 2005) and in its association with anthropogenic emissions of greenhouse gases (Intergovernmental Panel on Climate Change , 2007). The climate in the western United States warmed in concert with the global trend but at an accelerated rate (+0.8°C during the 20th century; Saunders and others, 2008). The region could also prove especially sensitive to future changes because the relatively small human population is growing rapidly, as are demands on limited water supplies. Regional hydrological patterns are dominated by seasonal snow accumulation at upper elevations. Most of the region is relatively dry, and both terrestrial and aquatic ecosystems are strongly constrained b y water availability (Barnett and others, 2008; Brown and others, 2008). Stream environments are dynamic and climatically extreme, and salmonid fishes are the dominant elements of the native biodiversity (McPhail and Lindsey, 1986; Waples and others, 2008). Salmonids have broad economic and ecologic importance, but a century of intensive water resource development, nonnative fish stocking, and land use has significantly reduced many populations and several taxa are now protected under the Endangered Species Act (Thurow and others, 1997; Trotter, 2008). Because salmonids require relatively pristine, cold water environments and are often isolated in headwater habitats, members of this group may be especially vulnerable to the effects of a warming climate (Keleher and Rahel, 1996; Rieman and others, 2007; Williams and others, 2009). Warming during the 20th century drove a series of environmental trends that have profound implications for many aspects of salmonid habitat, including disturbance regimes such as wildfire, and unfavorable changes to thermal and hydrologic properties of aquatic systems. Warmer air temperatures have been associated with decreased winter snow accumulations, have accelerated snowmelt, and have advanced the timing of peak runoff by several days to weeks across most of western North America (Stewart and others, 2005; Barnett and others, 2008). Less snow and earlier runoff decrease aquifer recharge, make less water available for groundwater inputs to streams, and are contributing to widespread decreases in summer low flows (Stewart and others, 2005; Rood and others, 2008; Luce and Holden 2009). Interannual variability in stream flow is increasing, as is the persistence of multi-year extreme conditions (McCabe and others, 2004; Pagano and Garen 2005). In many areas of western North America, flood risks have increased in association with warmer temperatures during the 20th century (Hamlet and Lettenmaier, 2005). Streams where midwinter temperatures are near freezing have proven especially sensitive to increased flooding because of associated transitional hydrological patterns (mixtures of rainfall and snowmelt) and propensity for occasional rain-on-snow events to rapidly melt winter snowpack and generate large floods (Hamlet and Lettenmaier, 2005). Stream temperatures in many areas are increasing (Peterson and Kitchell, 2001; Morrison and others, 2002; Bartholow, 2005; Kaushal and others, 2010), due to both air temperature increases and reduced summer flows that make streams more sensitive to warmer air temperatures (Isaak and others, 2010). In recent decades, wildfires have become more common across much of the western United States during periods of more frequent droughts (Westerling and others, 2006; Hoerling and Eischeid, 2007), and local stream temperature can increase in postfire environments (Gresswell, 1999; Dunham and others, 2007). Fire-related temperature increase within streams is commonly a transient phenomenon, lasting only until riparian vegetation has recovered (Gresswell, 1999); however, ongoing climate change could preclude recovery to higher stature, prefire vegetation types in some areas (McKenzie and others, 2004; van Mantgem and Stephenson, 2007), resulting in a loss of critical riparian shading. Additionally, when wildfires occur in steep mountain topographies, the vegetation that stabilize s soils on hillslopes is often killed and landslides become more prevalent (Gresswell, 1999). Landslides int o stream channels form debris flows composed of sediment slurries and dead trees that can scour channels to bedrock and further exacerbate stream heating, delay recovery of riparian areas, or extirpate fish populations (Gresswell, 1999; May and Gresswell, 2003; Dunham and others, 2007). Changes in stream environments will shift habitat distributions, sometimes unpredictably, in both time and space for many salmonid fishes. Water temperature fundamentally influences aquatic ecosystem health because distribution, reproduction, fitness, and survival of ectothermic organisms are inextricably linked to the thermal regime of the environment. Historically, research has focused on defining lethal thermal limits of salmonids (Eaton and others, 1995; Selong and others, 2001; Todd and others, 2008); however, water temperature is known to be important in biological processes at a variety of spatial scales and levels of biological organization (Rahel and Olden, 2008; McCullough and others, 2009). For instance, trout are affected directly by water temperature through feeding, metabolism, and growth rates, and indirectly by factors such as prey availability and species interactions (Wehrly and others, 2007; Rahel and Olden, 2008). Where cold water temperatures currently limit habitat suitability and distributions of some species (for example, at the highest and most northerly distributional extents; Nakano and others, 1996; Coleman and Fausch, 2007), a warming climate may gradually increase the quality and extent of suitable habitat. Over time, previously constrained populations are expected to expand into these new habitats and increase in number. Some evidence suggests this may already be happening in Alaska, where streams in recently deglaciated areas are being colonized by emigrants from nearby salmon and char populations (Milner and others, 2000). Unfortunately, many of the sensitive salmonid species that are often the focus of western managers are unlikely to benefit from future water temperature increases. Warmer stream temperatures will facilitate invasion by nonnative species that are broadly established in downstream areas into upstream areas where they will compete with native species (Rieman and others, 2006; Rahel and Olden, 2008; Fausch and others, 2009). In other cases, warmer stream temperatures will render thermally suitable habitats unsuitable in downstream areas and effect net losses of habitat because upstream distributions are often constrained by streams that are too small or steep (Hari and others, 2006; Isaak and others, 2010). Both scenarios are realistic for fish species like bull trout ( Salvelinus confluentus ) (Rieman and others, 2006; Rieman and others, 2007), the various subspecies of cutthroat trout ( Oncorhynchus clarkii ) (Williams and others, 2009), Gila trout ( Oncorhynchus gilae gilae ) (Kennedy and others, 2008), and Apache trout ( Oncorhynchus gilae apache ) (Rinne and Minckley, 1985; Carmichael and others, 1993). As native species are increasingly confined to smaller and more isolated habitats by a gradually warming climate, the effects of wildfires (whether related to lethal changes in water quality during a fire, channel debris flows, or chronic postfire warming ) could have greater proportional effects on remaining habitats (for example, Brown and others, 2001; Rieman and others, 2007). If these changes were accompanied by additional hydrologic alterations associated with changes to the magnitude, frequency, duration, timing, and rate of change of discharge patterns (Jager and others, 1999; Henderson and others, 2000), populations may begin to lose some of their historic resilience and become ever more susceptible to local extirpations. As dramatic and extensive as climatic and environmental trends are for salmonid habitats, global climate models (GCMs) project that many of these trends will continue and even accelerate until at least the middle of the 21st century (Intergovernmental Panel on Climate Change, 2007). Current projections suggest mean annual air temperatures will increase by an additional 1–3°C, and early indications are that climate trajectory is at the higher end of this range (Pittock, 2006; Raupach and others, 2007). Although predicted changes vary considerably, even the most conservative estimates suggest a warming rate that will be twice that observed during the 20th century. Projections for the midcentury are most certainly due to the effects of greenhouse gases already emitted or predicted in the short term, uncertainties of the effects of longer-term greenhouse gas emissions, short-term climate cycles, and process errors associated with climate models (Cox and Stephenson, 2007). Projections of changes in total precipitation are less certain than those for air temperatures, but most GCMs project relatively small changes in the Northwest, with the exception of slightly drier summer periods (Mote and others, 2008; Karl and others, 2009). In the Southwest, however, significant decreases (such as 15–30 percent ) are projected during most periods of the year, and this area is one of the few for which Intergovernmental Panel on Climate Change (2007) precipitation projections have a high level of certainty (Hoerling and Eischeid, 2007; Karl and others, 2009). Clearly, managers of native salmonids in the wester n United States should consider adjusting management strategies to accommodate a warmer and possibly drier future (Williams and others, 2009). Tools are needed to forecast where important changes may occur and how conservation efforts should be prioritized. In this Open-File Report, we document our initial efforts in this regard for 10 species and subspecies of inland trout and Montana Arctic grayling ( Thymallus arcticus ) across the western United States.

Arizona, California, Colorado, Idaho, Montana, Nev↗

Assessing causes of mortality for endangered juvenile Lost River suckers (Deltistes luxatus) in mesocosms in Upper Klamath Lake, south-central Oregon, 2016

Executive Summary The recovery of endangered Lost River suckers ( Deltistes luxatus ) in Upper Klamath Lake, south-central Oregon, has been impeded because juveniles are not recruiting into adult spawning populations. Adult sucker populations spawn each spring but mortality of age-0 suckers during their first summer is excessively high, and recruitment of juveniles into adult populations does not occur in most years. The last significant year class to join spawning aggregations was hatched in 1991. Capture rates for age-0 Lost River suckers decrease so substantially each summer that it is thought that mortality is nearly 100 percent within the first year of life each year. Causes of mortality are not understood but poor water quality, parasites, disease, predation, and non-native species are suspected to contribute to mortality. Upper Klamath Lake is hypereutrophic and summer water-quality conditions have large diurnal and seasonal fluctuations. Photosynthesis of Aphanizomenon flos-aquae , the most abundant cyanobacterium in Upper Klamath Lake, is responsible for large fluctuations in dissolved-oxygen (DO) concentrations and pH. We introduced hatchery-raised, passive integrated transponder-tagged juvenile Lost River suckers into large mesocosms located at Fish Banks, Mid North, and Rattlesnake Point in Upper Klamath Lake, Oregon, to assess sucker mortality relative to water-quality conditions. We identified the date of death for each sucker by assessing movement patterns among vertically stratified antennas. We modeled daily mortality using known fate models relative to water-quality conditions measured by sondes. Histopathology was used to understand causes of eminent mortality for moribund suckers. Fish mortality, growth, health, and movement patterns varied among locations, but it was unclear whether this variation was due to water-quality or other factors. Seasonal mortality was 58.8 percent at Fish Banks, 27.4 percent at Mid North, and 11.5 percent at Rattlesnake Point. Growth over the 109-day study period was lowest at Fish Banks (34.5 ±10.0 millimeters [mm] standard length (SL); 18.6 ±7.7 grams [g]), intermediate at Mid North (57.5 ±13.6 mm SL; 40.1 ±15.4 g), and greatest at Rattlesnake Point (78.4 ±13.0 mm SL; 72.5 ±18.7 g). Our ability to assess causes of juvenile sucker mortality in mesocosms using our modelling approach was limited by low daily mortality. Zero to 3 mortalities occurred per day, except on July 30 at Fish Banks when 7 mortalities occurred. Relative to any other measured and tested water-quality condition, mortality was more likely to occur on days with large fluctuations in oxygen percent saturation. When we assessed the fit of the most parsimonious model, performance was poor, which suggested that other factors were contributing to mortality. Our ability to assess the relationship between seasonal patterns in water quality and fish mortality were limited by the absence of substantial differences in water quality among sites, inconsistency in the depth at which measurements were collected, and no clear pattern in conditions leading up to and during mortality events. Except for DO at Rattlesnake Point and diel temperature variations at Fish Banks, seasonally summarized water-quality factors were similar among sites. The locations of water-quality monitors within the water column likely explain the differences in DO at Rattlesnake Point and temperature variation at Fish Banks. Furthermore, DO concentrations and other water-quality factors occurring during and prior to mortality events were inconsistent. Microscopic assessments indicated severe gill hyperplasia, fusion of the secondary lamellae, and severe Ichthyobodo sp. infestations on the gills of most moribund suckers. Liver glycogen was usually depleted in suckers with severe Ichthyobodo sp. infestations. Ichthyobodo sp. infestations probably were the immediate cause of death and probably originated from the Klamath Tribes Fish Research Facility, although this parasite also is present in Upper Klamath Lake and severe water-quality conditions may have contributed to morbidity. As suckers in the mesocosms died, they were replaced with suckers from the Fish Research Facility that likely were heavily parasitized with Ichthyobodo sp. Therefore, it is possible that the gradient in mortality rate among sites was owing to site-varying differences in inadvertent increases in introduced parasite loads.

Oregon↗