USGS Science⌕ Search

SEARCH · USGS Science

Results for “Growth”

Search indexed USGS publications on groundwater, aquifers, geologic maps, mineral resources and earthquakes. Explore source records by subject and place.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 919 records · Page 51Linked to original sources

Regeneration patterns of northern white cedar, an old-growth forest dominant

Regeneration of Thuja occidentalis L. was examined in an old-growth dune forest on South Manitou Island, Michigan. To estimate the current status of cedar regeneration, we determined size structure of seedlings and stems and analyzed present patterns of establishment and persistence relative to substrate type. There has been a shift in the pattern of cedar establishment from soil to log substrates. While 97% of all stems ≥15 cm dbh are associated with a soil substrate, 81% of stems ≥2.5cm-<15 cm dbh, and 98% of all cedar seedlings are confined to log substrates. However, few cedar seedlings survive; only 1% of all seedlings on logs are >25 cm tall. There was no significant relationship between the state of log decay and the density of seedlings >25 cm in height, indicating that long-term survival is not dependent on the degree of log decomposition. However, survival on logs is associated with canopy openings. Seedlings >25 cm tall were associated with gaps, and 78% of cedar stems (≥2.5 cm dbh) on logs were associated with a single windthrow gap. Thus, current cedar regeneration in this old-growth forest depends on logs and the canopy openings associated with them.

American Midland Naturalist↗

Salinity as a constraint on growth of oligohaline marsh macrophytes. II. Salt pulses and recovery potential

The ability of common oligohaline marsh macrophytes of the northern Gulf of Mexico coast to recover from pulses of increased salinity was investigated in a greenhouse experiment with Eleocharis palustris, Panicum hemitomon, Sagittaria lancifolia, and Scirpus americanus monocultures. Components of salinity pulses applied were final salinity reached (6 or 12 g/L), salinity influx rate (3 d or 3 wk), and duration of exposure (1, 2, or 3 mo). After each exposure period, we placed plants into freshwater until the end of the 120-d experiment to determine recovery potential. The four species varied in their ability to recover from the salinity pulses. Within a species, recovery varied with final salinity level and duration of exposure, and to a lesser extent with salinity influx rate. Scirpus americanus, growth of which was stimulated by <3 mo of exposure to 6 g/L, was able to recover even under the most extreme conditions of exposure to 12 g/L salinity for 3 mo. Ability to recover decreased with increased salinity and increased duration of exposure for the remaining three species. Recovery of specific aspects of growth was also suppressed in these species by a rapid salinity influx rate compared to a slow influx rate. The complex variations in recovery patterns displayed by the different species may lead to changes in species dominance following the short-term salinity pulses that can occur during storm events, which in turn may affect marsh plant community composition and structure.

Louisiana↗

Growth rate is negatively correlated with hatch date in Black Brant

Arctic geese nest in a highly seasonal environment in which ungrazed plants reach peak nitrogen concentrations when goslings hatch (Sedinger and Raveling 1986). Grazing by geese prolongs peak nutrient concentrations but reduces food availability. This should cause nutrient availability to decline seasonally. Here, we test the hypothesis that late-hatching goslings of Black Brant ( Branta bernicla nigricans ) grow more slowly than those hatching early. We substracted the sizes of wild goslings from those of captive-reared goslings of the same age and regressed the differences against hatch date. Differences between wild- and captive-reared goslings for body mass, tarsus length, and culmen length were significantly negatively related to hatch date; i.e., late-hatching wild goslings were smaller than those hatching early, after accounting for age. We detected no between-year difference in gosling size, but male goslings were larger than females of the same age for all measures. Egg size was only weakly associated with size of goslings 1 mo after hatching, but we detected no effect of other brood characteristics on growth. Seasonal variation in gosling growth rate may favor early nesting in arctic geese.

Alaska↗

Elk and deer diets in old-growth forests in western Washington

Dietary quality and overlap of sympatric Roosevelt elk ( Cervus elaphus roosevelti ) and Columbian black-tailed deer ( Odocoileus hemionus columbianus ) were investigated in old-growth forests of the Hoh Valley, Olympic National Park, Washington. Diets of both cervids were comprised mainly of common old-growth flora, particularly in winter. High dietary overlap suggested competitive interactions for food, especially in winter when forage resources were least available. Predominant forages in fall and winter diets seemed to afford little opportunity for cervids to select different plant parts. Crude protein (CP), in vitro dry matter digestibility (IVDMD), and phosphorus (P) in important forages varied with phenology, but seasonal trends were more pronounced for shrubs and grasses than forbs and trees. CP, IVDMD, and P in cervid diets also varied seasonally and usually in the following ascending order: winter, fall, summer, spring. CP and P appeared to be adequate in diets, but low IVDMD suggested that digestible energy was limited. Few significant differences in seasonal dietary qualities were demonstrated between elk and deer. The collective cervid population (and its habitat) in the Hoh Valley is unmanaged and probably at equilibrium with its food resource, or at ecological carrying capacity. Results are discussed in light of herbivore--habitat interactions at equilibrium densities.

Washington↗

Effects of forest management on density, survival, and population growth of wood thrushes

Loss and alteration of breeding habitat have been proposed as causes of declines in several Neotropical migrant bird populations. We conducted a 4-year study to determine the effects of winter prescribed burning and forest thinning on breeding wood thrush ( Hylocichla mustelina ) populations at the Piedmont National Wildlife Refuge (PNWR) in Georgia. We estimated density, adult and juvenile survival rates, and apparent annual survival using transect surveys, radiotelemetry, and mist netting. Burning and thinning did not cause lower densities ( P = 0.25); wood thrush density ranged from 0.15 to 1.30 pairs/10 ha. No radiomarked male wood thrushes ( n = 68) died during the 4 years, but female ( n = 63) weekly survival was 0.981 ± 0.014 (SE) for females ( n = 63) and 0.976 ± 0.010 for juveniles ( n = 38). Apparent annual adult survival was 0.579 (SE = 0.173). Thinning and prescribed burning did not reduce adult or juvenile survival during the breeding season or apparent annual adult survival. Annual population growth (lambda) at PNWR was 1.00 (95% confidence interval = 0.32-1.63), and the considerable uncertainty in this prediction underscores the need for long term monitoring to effectively manage Neotropical migrants. Population growth increased on experimental compartments after the burn and thin (95% CI before = 0.91-0.97, after = 0.98-1.05), while control compartment declined (before = 0.98-1.05, after = 0.87-0.92). We found no evidence that the current management regime at PNWR, designed to improve red-cockaded woodpecker ( Picoides borealis ) habitat, negatively affected wood thrushes.

Georgia↗

Marrow fat deposition and skeletal growth in caribou calves

I evaluated rates of marrow fat deposition and skeletal growth of caribou ( Rangifer tarandus granti ) calves through 20 days of age at Denali National Park, Alaska, USA. Both were negatively correlated with late winter snowfall, indicating the prolonged effects of maternal undernutrition following severe winters. Using regression analyses, I found that the rates of marrow fat deposition and hindfoot growth during the 20 days following birth declined 46% and 68%, respectively, over the range of winter severity during this study. These measures of development may indicate a broader array of effects of maternal undernutrition, influencing the vulnerability of caribou calves to predation.

Journal of Wildlife Management↗

Growth and development of the king rail

Growth and development of the King Rail ( Rallus elegans ) from hatching to first flight were studied by observations and measurements of captive birds and by observations of natural nests in the field. This is the fourth in a series of reports on the life history of the King Rail (Meanley 1953, 1956, and 1957). Information in this paper is intended to supplement the data of Bent (1925) on growth and development and the description of juvenal plumage given by Friedmann (1941).

The Auk↗

Growth and equilibrium in sea otter populations

(1) Counts through time were compiled for five sea otter ( Enhydra lutris ) populations in the north-east Pacific Ocean that were below equilibrium density: Attu Island, south-east Alaska, British Columbia, Washington State, and central California. Similar data were obtained from the equilibrium density population at Amchitka Island in 1971 and 1986. (2) Shorelines of Attu and Amchitka islands each were divided into forty-five segments, within which lineal (length of shore at mean higher high water) and areal (mean higher high water to the 10-fathom (18.3-m) depth contour) measures were made of the amount of habitat. (3) Rate of increase for the four northern populations was 17-20% year-1. Density- or size-dependent changes in rate of increase could not be demonstrated for any of these populations. The California population, in contrast, has undergone three apparent growth phases: the early 1900s to the mid-1970s when it increased about 5% year-1; the mid-1970s to the mid-1980s when it declined about 5% year-1; and the mid-1980s to 1988 when it increased about 7% year-1. An exponential growth model accounted for 92-98% of the variation in counts through time in all cases. (4) Population increase at Attu Island was achieved largely by range expansion as opposed to increased density. Range expansion in lineal and areal habitat occurred at 11% and 13% year-1, respectively; neither rate was lower (P > 0.25) than the observed rate of increase in numbers of animals counted. (5) Despite similarities in island size and physical environment, the most conservative estimates of population density at Amchitka Island were > 3 X greater than maximum density estimates for Attu Island. (6) Surveys of Amchitka Island from the mid-1930s through the mid-1980s indicate that the population increased to a peak in the 1940s; declined abruptly thereafter; and subsequently increased to a new and higher equilibrium in the 1960s, where it has since remained. (7) These population data, together with information on sea otter foraging and benthic community structure at Attu and Amchitka islands, suggest that multiple population equilibria exist in this system, emanating from complex trophic interactions low in the food web. I hypothesize that the lower population equilibrium is achieved largely or exclusively on an invertebrate diet consisting principally of herbivorous sea urchins. When unregulated by sea otter predation, the rocky benthos is deforested by sea urchin grazing. As growing otter populations compete increasingly for food, grazing intensity declines and the system shifts to one dominated by kelp beds, in turn leading to increased production, a shift in habitat structure, and population increases of kelp bed fishes. Apparently this new food resource elevates the sea otter population to a higher and more stable equilibrium.

Journal of Animal Ecology↗

Dose-response effects of recombinant bovine somatotrop (Posilac) on growth performance and body composition of two-year-old rainbow trout (Oncorhynchus mykiss)

Two hundred rainbow trout ( Oncorhynchus mykiss , mean weight 301.5 g) were allotted to four treatments with five replicates in a randomized block design to determine the dose-response effects of recombinant bovine somatotropin (rbST; Posilac TM ) on growth performance and carcass composition. Treatments were sham-injected controls (S), 10 µ g/g BW of rbST (L), 20 µ g/g BW of rbST (M), and 30 µ g/g BW of rbST (H). The tanks held 135 L; water flow = 15.1 L/min; temperature = 15°C. The fish were maintained in a 12-h light:dark cycle and hand-fed twice daily. The fish received a single intraperitoneal (i.p.) injection on d 0 and were weighed on d 0, 14, 28, and 56. On d 56 the fish were killed. The whole body (WBW), eviscerated carcass (EC), viscera (VIS), and reproductive organ weights and the increase in average daily body length (ADL) were determined. Recombinant bST reduced (linear, P < .004) feed intake 17.6% from d 0 to 14 and improved ADG 44.8% from d 0 to 14 (linear, P < .001) and 8.1% from d 0 to 56 (linear, P < .022). Treated groups had improved (linear, P < .001) feed efficiencies for d 0 to 28. Treatment with rbST increased final weight (linear, P < .018) and length (linear, P < .001), decreased carcass dry matter (linear, P < .001) and fat (linear, P < .001), content, increased carcass ash (linear, P < .001) and tended to increase carcass protein (linear, P < .054) content. Recombinant bST increased WBW (linear, P < .018) and EC (linear, P < .003) but decreased (linear, P < .015) testes weight. Ovary weights, VIS and overall gonadosomatic index were unaffected ( P > .05) by rbST. Recombinant bST was undetectable in serum samples taken on d 56 as determined by radioimmunoassay. Overall, the improved ADG, feed efficiency, body mass, and composition indicate that administration of rbST to rainbow trout may be an efficacious method of modulating growth in fish.

Journal of Animal Science↗

Reserve growth effects on estimates of oil and natural gas resources

Many scientists think that the supply of economically recoverable oil and natural gas is geologically limited. However, as recently as early 1999, we experienced a glut of oil on the world market and the lowest inflation-adjusted price of gasoline in history. What is going on? While we cannot provide a comprehensive answer to that question here, we can describe one process that significantly affects the domestic oil and gas industry, a process that also will affect the global industry at some point—reserve growth (also known as field growth).

Fact Sheet↗

Monitoring and analysis of sand dune movement and growth on the Navajo Nation, southwestern United States

Recurring drought and rising temperatures have caused reactivation and renewed growth of sand dunes on the lands of the Navajo Nation on the Colorado Plateau. Migrating dunes threaten health, housing, and transportation pathways. U.S. Geological Survey (USGS) scientists are conducting research to better understand the processes of dune growth and movement. This research will provide critical data to the Native peoples of the region in their response to the changing environment.

Colorado Plateau↗

Juvenile Lost River and shortnose sucker year-class formation, survival, and growth in Upper Klamath Lake, Oregon and Clear Lake Reservoir, California—2017 Monitoring Report

Executive Summary Populations of federally endangered Lost River ( Deltistes luxatus ) and shortnose suckers ( Chasmistes brevirostris ) in Upper Klamath Lake, Oregon, and Clear Lake Reservoir (hereinafter referred to as Clear Lake; fig. 1), California, are experiencing long-term declines in abundance. Upper Klamath Lake populations are decreasing because juvenile suckers are not surviving and recruiting into the adult population. Most juvenile sucker mortality occurs within the first year of life in Upper Klamath Lake. Annual production of juvenile suckers in Clear Lake appear to be highly variable and may not occur at all in very dry years. However, juvenile sucker survival is much higher in Clear Lake, with some suckers surviving to join spawning aggregations. Long-term monitoring of juvenile sucker populations is needed to 1) determine if there are annual and species-specific differences in production, survival, and growth; 2) better understand when juvenile sucker mortality is greatest; 3) help identify potential causes of high juvenile sucker mortality particularly in Upper Klamath Lake; and 4) monitor for successful juvenile survival in Upper Klamath Lake. The U.S. Geological Survey (USGS) began a summer juvenile sucker monitoring program in 2015 to track cohorts over time in Upper Klamath and Clear Lakes. The juvenile sucker monitoring program involved using trap net data at fixed sites to determine the status of juvenile suckers. Annual variability in apparent age-0 sucker production, juvenile sucker survival, and growth were tracked. Using genetic markers, suckers were classified as one of three taxa; shortnose (combinations of shortnose and Klamath largescale suckers), Lost River, or suckers with genetic markers of both species (Intermediate [Prob]). By using catch data, we generated taxa-specific indices of year-class strength, August–September apparent survival, and overwinter apparent survival. We also examined the prevalence and severity of afflictions such as parasites, wounds, and deformities. The Upper Klamath Lake year-class strength indices for both Lost River and shortnose suckers were slightly lower in 2015 and 2017 than in 2016. The ratios of age-0 Lost River suckers to age-0 shortnose suckers captured in August in Upper Klamath Lake were low in 2015 and 2017, given that adult Lost River suckers are more abundant and more fecund than adult shortnose suckers. This may indicate lower egg, larval, or juvenile survival or poorer spawning success for Lost River suckers than shortnose suckers in these two years. Apparent relative age-0 survival indices for Lost River suckers from August to September in Upper Klamath Lake were greater in 2015 (0.29) than in 2016 (0.16) or 2017 (0.14). Age-0 shortnose sucker catch rates increased between August and September in 2015, possibly indicating new individuals of this species were still recruiting to the lake between the two sampling periods. August to September relative survival indices for Upper Klamath Lake shortnose suckers were 0.35 in 2016 and 0.00 in 2017. We predicted year-class strength would be greater in Clear Lake in years when high spring-time lake elevations and instream flow allowed adult suckers access to spawning habitat in the Willow Creek drainage. Instream flows and lake elevations were sufficient to allow adult suckers to access Willow Creek during the 2016 and 2017 spawning seasons, and age-0 suckers were detected in Clear Lake both years. Higher lake surface elevations and instream flows in 2017 than in 2016 were not associated with higher year-class strength indices in 2017 than in 2016. Low lake surface elevations appeared to limit access by adults to Willow Creek during the 2014 and 2015 spawning seasons and age-0 suckers were not detected in Clear Lake during these years. Nineteen shortnose suckers from the 2014 cohort were captured in Clear Lake in 2017. A 2015 cohort of shortnose suckers was captured as age-1 in 2016 and as age-2 in 2017. The most likely explanation for increasing catch rates of the 2015 cohort is that the higher Willow Creek flows in 2016 and 2017 facilitated the movement of stream-resident suckers, spawned in 2014 and 2015 downstream into Clear Lake. Due to uncertainty in the genetic identification of non-Lost River suckers, these fish are equally likely to be Klamath largescale or shortnose suckers (Hoy and Ostberg, 2015).

California, Oregon↗

Juvenile Lost River and shortnose sucker year-class formation, survival, and growth in Upper Klamath Lake, Oregon, and Clear Lake Reservoir, California—2018 monitoring report

Executive Summary Populations of federally endangered Lost River ( Deltistes luxatus ) and shortnose suckers ( Chasmistes brevirostris ) in Upper Klamath Lake, Oregon, and Clear Lake Reservoir (hereinafter Clear Lake), California, are experiencing long-term decreases in abundance. Upper Klamath Lake populations are decreasing not only because of adult mortality, which is relatively low, but also because they are not being balanced by recruitment of young adult suckers into known adult spawning aggregations. Long-term monitoring of juvenile sucker populations is conducted to (1) determine if there are annual and species-specific differences in production, survival, and growth; (2) better understand when juvenile sucker mortality is greatest, and (3) help identify potential causes of high juvenile sucker mortality, particularly in Upper Klamath Lake. The U.S. Geological Survey monitoring program, which began in 2015, tracks cohorts through summer months and among years in Upper Klamath and Clear Lakes. Data on juvenile suckers captured in trap nets are used to provide information on annual variability in age-0 sucker apparent production, juvenile sucker apparent survival, apparent growth, species composition, and health. Juvenile sucker year-class strength and apparent survival were low in 2018 in Upper Klamath Lake. Most juvenile sucker mortality occurs within the first year of life. The Upper Klamath Lake year-class strength indices for Lost River and shortnose suckers in 2018 were the lowest they had been since the start of monitoring in 2015. The annual catch rates of shortnose sucker remained consistently low, whereas Lost River sucker catch rates varied. The capture of only four age-1 and older suckers from Upper Klamath Lake during the 2018 sampling season indicated low annual survival of the 2017 cohort. Annual production indices of juvenile suckers in Clear Lake are highly variable and potentially affected by seasonal connections to spawning habitat in Willow Creek. A total of seven age-0 shortnose or Klamath largescale suckers ( Catostomus snyderi ) were captured from Clear Lake in 2018, which was a relatively wet year, indicating that a small cohort was formed or that there was a delay in the recruitment of age-0 suckers. The 2018 sampling continued to detect recruitment of juveniles from the 2015 cohort to the lake. Given the dysconnectivity between Willow Creek and Clear Lake during the 2015 spawning season, the continued recruitment of young fish of this cohort to the lake may be attributed to reproduction by resident suckers in Willow Creek. Suckers younger than age-3 in Clear Lake could be identified as either shortnose or Klamath largescale suckers. A stream resident life history, if it were occurring, is consistent with these fish being Klamath largescale suckers. Survival of all distinguishable taxa of juvenile suckers is much higher in Clear Lake than in Upper Klamath Lake, with non-trivial numbers of suckers surviving to join spawning aggregations.

California, Oregon↗

Growth, survival, and cohort formation of juvenile Lost River (Deltistes luxatus) and shortnose suckers (Chasmistes brevirostris) in Upper Klamath Lake, Oregon, and Clear Lake Reservoir, California—2019 Monitoring Report

Populations of federally endangered Lost River ( Deltistes luxatus ) and shortnose suckers ( Chasmistes brevirostris ) in Upper Klamath Lake, Oregon, and Clear Lake Reservoir (hereinafter, Clear Lake), California, are experiencing long-term decreases in abundance. Upper Klamath Lake populations are decreasing not only due to adult mortality, which is relatively low, but also because they are not being balanced by recruitment of young adult suckers into known adult spawning aggregations. Long-term monitoring of juvenile sucker populations is conducted to (1) determine if there are annual and species-specific differences in production, survival, and growth, (2) better understand when juvenile sucker mortality is greatest, and (3) help identify potential causes of high juvenile sucker mortality particularly in Upper Klamath Lake. The U.S. Geological Survey monitoring program, that began in 2015, tracks cohorts through summer months and among years in Upper Klamath and Clear Lakes. Data on juvenile suckers captured in trap nets are used to provide information on annual variability in age-0 sucker apparent production, juvenile sucker apparent survival, apparent growth, species composition, and health. Upper Klamath Lake indices of year-class strength indicated that the 2019 year-class was the strongest in the past 5 years of monitoring. Low detections of age-1 and older suckers indicate that the 2018 cohort experienced poor survival within the first year of life. Shortnose suckers constituted the smallest proportion and suckers with uncertain species identification constituted the largest proportion of the 2019 year-class. Small numbers of Lost River sucker were captured consistently throughout the sampling season. The relative abundance of age-0 suckers is not a good indicator of year-class strength in Clear Lake. There were no age-0 suckers captured in Clear Lake during the 2015 and 2019 sampling seasons. Most suckers captured were age-1 Klamath largescale/shortnose suckers, which indicated a relatively strong 2018 cohort. Four-year old juveniles from the 2015 cohort were present in 2019 in Clear Lake. Cohorts that do not recruit to our sampling gear until a year or more of age seem to indicate that (1) a stream resident life history is contributing to the lake population and (2) juvenile suckers occupy the Willow Creek drainage for a full year or more. Although these suckers could be either the non-endangered Klamath largescale or the endangered shortnose suckers, a stream resident life history is consistent with these fish being Klamath largescale suckers. Survival of all distinguishable taxa of juvenile suckers is much higher in Clear Lake than in Upper Klamath Lake, with non-trivial numbers of suckers surviving to join spawning aggregations in most years.

California, Oregon↗

Growth, survival, and cohort formation of juvenile Lost River (Deltistes luxatus) and shortnose suckers (Chasmistes brevirostris) in Upper Klamath Lake, Oregon, and Clear Lake Reservoir, California—2020 monitoring report

Executive Summary Populations of federally endangered Lost River ( Deltistes luxatus ) and shortnose suckers ( Chasmistes brevirostris ) in Upper Klamath Lake, Oregon, and Clear Lake Reservoir (hereinafter, Clear Lake), California, are experiencing long-term decreases in abundance. Upper Klamath Lake populations are decreasing not only because of adult mortality, which is relatively low, but also because they are not being balanced by recruitment of young adult suckers into known adult spawning aggregations. Long-term monitoring of juvenile sucker populations is conducted to (1) determine if there are annual and species-specific differences in production, survival, and growth, (2) better understand when juvenile sucker mortality is greatest, and (3) help identify potential causes of high juvenile sucker mortality particularly in Upper Klamath Lake. The U.S. Geological Survey (USGS) monitoring program, begun in 2015, tracks cohorts through summer months and among years in Upper Klamath and Clear Lakes. Data on juvenile suckers captured in trap nets are used to provide information on annual variability in age-0 sucker apparent production, juvenile sucker apparent survival, apparent growth, species composition, and health. Upper Klamath Lake indices of year-class strength suggest that the 2020 age-0 cohort is one of the lowest since standardized monitoring began. Despite apparently low over-winter survival, the relatively large 2019 cohort persisted in our 2020 samples and continues to contribute to the populations. Although the 2019 cohort age-0 suckers were composed mainly of Lost River suckers, the age-1 suckers from the 2019 cohort were mainly shortnose suckers. Lost River suckers comprised the largest proportion of the 2020 year-class and were only captured in July and August. Shortnose suckers were mainly captured in August and September and comprised a smaller proportion of the 2020 year-class. Age distribution of suckers captured in Clear Lake indicates greater juvenile survival than in Upper Klamath Lake. Most juvenile suckers captured were age-3 and age-4 suckers classified as the combination of Klamath largescale suckers ( Catostomus snyderi ) and shortnose suckers from the Lost River Basin, from the 2016 and 2017 cohorts. A lack of age-0 suckers captured in Clear Lake during years with the low inflow or lake levels initially lead us to believe that low water prevented spawning and year class formation. However, recent data indicate that some cohorts that were not captured as age-0 suckers were detected in later years at age-1 or age-2. This finding indicates that juvenile suckers in Clear Lake may spend one or more years in the tributaries or that sampling efficacy for age-0 suckers varies among years because of water depth. The first 5 years of this monitoring program indicated different patterns in recruitment and survival of juvenile suckers between Upper Klamath and Clear Lakes. Since the monitoring program began in 2015, age-0 sucker catch rates, interpreted as indices of year-class strength, were greatest in Upper Klamath Lake in 2016 and 2019. In those years Lost River suckers made up the majority of age-0 sucker catches; however, in 2017 and 2020 the age-1 sucker catches from these cohorts were mainly composed of shortnose suckers or suckers with genetic markers of both Klamath largescale and shortnose suckers, indicating a low overwinter survival for Lost River suckers even when the age-0 catches were high. Age-0 suckers do not fully recruit to our sampling gear in Upper Klamath Lake until August, experience high mortality by September, and are almost undetectable by the following July or August in most years. In Clear Lake, suckers frequently are not captured until age-1 or age-2 and annual survival appears much greater.

California, Oregon↗

Growth, survival, and cohort formation of juvenile Lost River (Deltistes luxatus) and shortnose suckers (Chasmistes brevirostris) in Upper Klamath Lake, Oregon, and Clear Lake Reservoir, California—2021–22 monitoring report

Executive Summary The work reported in this publication provides updated data and interpretation for sampling years 2015 and 2022 of the juvenile monitoring project. The study objectives, background, study area, species description, and methods remained the same or similar throughout the years, while the executive summary, results, and discussion were updated each year. Therefore much of this paper was originally presented in previous reports (Bart and others 2020a, b; Bart and others, 2021; Burdick and others, 2016; Burdick and others, 2018; Martin and others, 2022) and is repeated here for the reader’s convenience. Populations of federally endangered Lost River ( Deltistes luxatus ) and shortnose suckers ( Chasmistes brevirostris ) in Upper Klamath Lake, Oregon, and Clear Lake Reservoir (hereinafter, Clear Lake), California, are experiencing long-term decreases in abundance. Upper Klamath Lake populations are decreasing not only because of adult mortality, which is relatively low, but also because they are not being balanced by recruitment of young adult suckers into adult spawning aggregations. Long-term monitoring of juvenile sucker populations is conducted to (1) determine if there are annual and species-specific differences in production, survival, and growth; (2) better understand when juvenile sucker mortality is greatest; and (3) identify potential causes of high juvenile sucker mortality particularly in Upper Klamath Lake. The U.S. Geological Survey (USGS) monitoring program, begun in 2015, tracks cohorts through summer months and among years in Upper Klamath and Clear Lakes. Data on juvenile suckers captured in trap nets are used to provide information on annual variability in age-0 sucker production, juvenile sucker apparent survival, growth, species composition, and health. Upper Klamath Lake indices of year-class strength suggest that the 2022 age-0 cohort is the lowest since standardized monitoring began. The 2021 cohort, like most cohorts, had moderately low catch rates their first year of life, with a steep drop off during the second year. Although the 2020 cohort persisted through the September 2022 sampling, this cohort was sparsely represented after the first year with no representatives from this cohort captured from July 2021 through July 2022. Despite apparently low fall through spring apparent survival, the relatively large 2019 cohort persisted in our 2020–21 samples, but has not been detected since June 2021. Klamath largescale ( Catostomus snyderi ) and shortnose suckers were only differentiated from each other starting in 2020. Shortnose suckers dominated the age-1 catch in 2020 and 2022, whereas age-1 Klamath largescale suckers were slightly more prevalent in 2021. Although there were occasionally age-2 and older suckers captured, none of these fish were Lost River suckers. Except for 2015, 2017, and 2021, there were more age-0 Lost River suckers than presumed shortnose suckers in Upper Klamath Lake. However, in all years sampled, there were more age-1 presumed shortnose suckers than Lost River suckers. Age distribution of suckers captured in Clear Lake indicates greater juvenile survival than in Upper Klamath Lake. Most juvenile suckers captured throughout the years were from the 2016 and 2017 cohorts; however, by 2022 most of these fish were no longer susceptible to standard trap nets and were not as prevalent in 2022 juvenile catches, and these suckers presumedly recruited to the adult population. As the 2016 and 2017 cohorts catches declined, so did the catch in overall numbers of suckers. Excluding age-0 catches, the 2016 cohort catches peaked at age-3 and the 2017 catches peaked at age-2. In 2022, the majority of the catch was composed of age-3 to age-5 suckers. The majority of suckers captured in Clear Lake during this multiyear project were classified as the combination of Klamath largescale suckers and shortnose suckers from the Lost River Basin, from the 2016 and 2017 cohorts. The few suckers identified as Lost River or definitive shortnose suckers were from the 2016 and 2017 cohorts. A lack of age-0 suckers captured in Clear Lake during years with low spawning tributary inflow or lake levels suggested that low water prevented spawning and year class formation. However, recent data indicate that some cohorts with Klamath largescale and shortnose sucker genetics that were not captured as age-0 suckers were detected in later years at age-1 or age-2. This finding indicates that juvenile suckers in Clear Lake may spend one or more years in the tributaries and that these cohorts may primarily be represented by Klamath largescale suckers. The first 7 years of this monitoring program indicated different patterns in recruitment and survival of juvenile suckers between Upper Klamath and Clear Lakes. Since the monitoring program began in 2015, age-0 sucker catch rates, interpreted as indices of year-class strength, were greatest in Upper Klamath Lake in 2016 and 2019. In those years, Lost River suckers made up the majority of age-0 sucker catches. However, in 2017 and 2020, the age-1 sucker catches from these cohorts were mainly composed of shortnose suckers or suckers with genetic markers of both Klamath largescale and shortnose suckers, indicating a low first year survival for Lost River suckers even when age-0 catches were high. Age-0 suckers do not fully recruit to our sampling gear in Upper Klamath Lake until August, experience high mortality by September, and are almost undetectable in subsequent years. In Clear Lake, suckers are often not captured until age-1 or age-2 and juvenile annual survival appears much greater; however, there does appear to be a drop-off in catch rates as the suckers age and become less susceptible to the fishing gear.

California, Oregon↗

Growth and degradation of Hawaiian volcanoes

The 19 known shield volcanoes of the main Hawaiian Islands&mdash;15 now emergent, 3 submerged, and 1 newly born and still submarine&mdash;lie at the southeast end of a long-lived hot spot chain. As the Pacific Plate of the Earth&rsquo;s lithosphere moves slowly northwestward over the Hawaiian hot spot, volcanoes are successively born above it, evolve as they drift away from it, and eventually die and subside beneath the ocean surface. The massive outpouring of lava flows from Hawaiian volcanoes weighs upon the oceanic crust, depressing it by as much as 5 km along an axial Hawaiian Moat. The periphery of subsidence is marked by the surrounding Hawaiian Arch. Subsidence is ongoing throughout almost all of a volcano&rsquo;s life. During its active life, an idealized Hawaiian volcano passes through four eruptive stages: preshield, shield, postshield, and rejuvenated. Though imperfectly named, these stages match our understanding of the growth history and compositional variation of the Hawaiian volcanoes; the stages reflect variations in the amount and rate of heat supplied to the lithosphere as it overrides the hot spot. Principal growth occurs in the first 1&ndash;2 million years as each volcano rises from the sea floor or submarine flank of an adjacent volcano. Volcanic extinction ensues as a volcano moves away from the hot spot. Eruptive-stage boundaries are drawn somewhat arbitrarily because of their transitional nature. Preshield-stage lava is alkalic as a consequence of a nascent magma-transport system and less extensive melting at the periphery of the mantle plume fed by the hot spot. The shield stage is the most productive volcanically, and each Hawaiian volcano erupts an estimated 80&ndash;95 percent of its ultimate volume in tholeiitic lavas during this stage. Shield-stage volcanism marks the time when a volcano is near or above the hot spot and its magma supply system is robust. This most active stage may also be the peak time when giant landslides modify the flanks of the volcanoes, although such processes begin earlier and extend later in the life of the volcanoes. Late-shield strata extend the silica range as alkali basalt and even hawaiite lava flows are sparsely interlayered with tholeiite at some volcanoes. Rare are more highly fractionated shield-stage lava flows, which may reach 68 weight percent SiO 2 . Intervolcano compositional differences result mainly from variations in the part of the mantle plume sampled by magmatism and the distribution of magma sources within it. Volcanism wanes gradually as Hawaiian volcanoes move away from the hot spot, passing from the shield stage into the postshield stage. Shallow magma reservoirs (1&ndash;7-km depth) of the shield-stage volcanoes cannot be sustained as magma supply lessens, but smaller reservoirs at 20&ndash;30-km depth persist. The rate of extrusion diminishes by a factor of 10 late in the shield stage, and the composition of erupted lava becomes more alkalic&mdash;albeit erratically&mdash;as the degree of melting diminishes. The variation makes this transition, from late shield to postshield, difficult to define rigorously. Of the volcanoes old enough to have seen this transition, eight have postshield strata sufficiently distinct and widespread to map separately. Only two, Ko&lsquo;olau and Lāna&lsquo;i, lack rocks of postshield composition. Five Hawaiian volcanoes have seen rejuvenated-stage volcanism following quiescent periods that ranged from 2.0 to less than 0.5 million years. The rejuvenated stage can be brief&mdash;only one or two eruptive episodes&mdash;or notably durable. That on Ni&lsquo;ihau lasted from 2.2 to 0.4 million years ago; on Kaua&lsquo;i, the stage has been ongoing since 3.5 million years ago. As transitions go, the rejuvenated stage may be thought of as the long tail of alkalic volcanism that begins in late-shield time and persists through the postshield (+rejuvenated-stage) era. Because successive Hawaiian volcanoes erupt over long and overlapping spans of time, there is a wide range in the age of volcanism along the island chain, even though the age of Hawaiian shields is progressively younger to the southeast. For example, almost every island from Ni&lsquo;ihau to Hawai&lsquo;i had an eruption in the time between 0.3 and 0.4 million years ago, even though only the Island of Hawai&lsquo;i had active volcanoes in their shield stage during that time. Once they have formed, Hawaiian volcanoes become subject to a spectrum of processes of degradation. Primary among these are subaerial erosion, landslides, and subsidence. The islands, especially those that grow high above sea level, experience mean annual precipitation that locally exceeds 9 m, leading to rapid erosion that can carve deep canyons in less than 1 million years. Hawaiian volcanoes have also been modified by giant landslides. Seventeen discrete slides that formed in the past 5 m.y. have been identified around the main Hawaiian Islands, and fully 70 are known along the Hawaiian Ridge between Midway Islands and the Island of Hawai&lsquo;i. These giant landslides displace large amounts of seawater to generate catastrophic giant waves (megatsunami). The geologic evidence for megatsunami in the Hawaiian Islands includes chaotic coral and lava-clast breccia preserved as high as 155 m above sea level on Lāna&lsquo;i and Moloka&lsquo;i. Large Hawaiian volcanoes can persist as islands through the rapid subsidence by building upward rapidly enough. But in the long run, subsidence, coupled with surface erosion, erases any volcanic remnant above sea level in about 15 m.y. One consequence of subsidence, in concert with eustatic changes in sea level, is the drowning of coral reefs that drape the submarine flanks of the actively subsiding volcanoes. At least six reefs northwest of the Island of Hawai&lsquo;i form a stairstep configuration, the oldest being deepest.

Hawaii↗

Water-level variations and their effects on tree growth and mortality and on the biogeochemical system at the phytoremediation demonstration site in Fort Worth, Texas, 1996-2003

In 1996, a field-scale phytoremediation demonstration project was initiated and managed by the U.S. Air Force at a site in western Fort Worth, Texas, using a plantation of 1-year-old stems harvested from branches of eastern cottonwoods during the dormant season (whips) and a plantation of 1-year-old eastern cottonwood seedlings (calipers). The primary objective of the demonstration project was to determine the effectiveness of eastern cottonwoods at reducing the mass of dissolved trichloroethene transported within an alluvial aquifer. The U.S. Geological Survey conducted a study, in cooperation with the U.S. Air Force, to determine water-level variations and their effects on tree growth and mortality and on the biogeochemical system at the phytoremediation site. As part of the study, water-level and water-quality data were collected throughout the duration of the project. This report presents water-level variations at periodic sampling events; data from August 1996 to January 2003 are presented in this report. Water levels are affected by aquifer properties, precipitation, drawdown attributable to the trees in the study area, and irrigation. This report also evaluates the effects of ground-water depth on tree growth and mortality rates and on the biogeochemical system including subsurface oxidation-reduction processes. Overall, both whips and calipers showed a substantial increase in height, canopy diameter, and trunk diameter over the first 3 years of the study. By the fifth growing season (September 2000), the height of the calipers varied predictably with height decreasing with increasing depth to ground water. Percent mortality was relatively constant at about 25 percent in the whip plantation in January 2003 where ground-water levels were less than 10 feet below land surface during the drought in September 2000. The mortality rate increased where the ground-water levels were greater than 10 feet below land surface and approached 90 percent where ground-water levels were between 12 and 13 feet. A decrease in molar ratio of trichloroethene to cis -dichloroethene was measured in ground water within and downgradient from the planted area over time. Decreases in these ratios appeared to be related to ground-water depth. The molar ratios of trichloroethene to cis -dichloroethene during the third growing season were relatively constant, between 3.0 and 4.0, in samples collected from wells across the site. By the end of the fifth growing season the lowest ratio was measured in areas where ground-water depth was less than 10 feet below land surface; these same areas had the lowest dissolved oxygen concentrations (0.93 to 1.7 milligrams per liter) and the highest dissolved organic carbon concentrations (1.6 to 1.8 milligrams per liter). This indicates that between the third and fifth growing seasons, a labile fraction of dissolved organic carbon had been introduced into the aquifer by the planted trees that was capable of stimulating reductive dechlorination of trichloroethene.

Texas↗