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At least 145 records · Page 8Linked to original sources
USGS2016

A synthesis of radial growth patterns preceding tree mortality

Tree mortality is a key factor influencing forest functions and dynamics, but our understanding of the mechanisms leading to mortality and the associated changes in tree growth rates are still limited. We compiled a new pan-continental tree-ring width database from sites where both dead and living trees were sampled (2970 dead and 4224 living trees from 190 sites, including 36 species), and compared early and recent growth rates between trees that died and those that survived a given mortality event. We observed a decrease in radial growth before death in ca. 84% of the mortality events. The extent and duration of these reductions were highly variable (1–100 years in 96% of events) due to the complex interactions among study species and the source(s) of mortality. Strong and long-lasting declines were found for gymnosperms, shade- and drought-tolerant species, and trees that died from competition. Angiosperms and trees that died due to biotic attacks (especially bark-beetles) typically showed relatively small and short-term growth reductions. Our analysis did not highlight any universal trade-off between early growth and tree longevity within a species, although this result may also reflect high variability in sampling design among sites. The intersite and interspecific variability in growth patterns before mortality provides valuable information on the nature of the mortality process, which is consistent with our understanding of the physiological mechanisms leading to mortality. Abrupt changes in growth immediately before death can be associated with generalized hydraulic failure and/or bark-beetle attack, while long-term decrease in growth may be associated with a gradual decline in hydraulic performance coupled with depletion in carbon reserves. Our results imply that growth-based mortality algorithms may be a powerful tool for predicting gymnosperm mortality induced by chronic stress, but not necessarily so for angiosperms and in case of intense drought or bark-beetle outbreaks.

Global Change Biology↗
USGS2021

Joint effects of climate, tree size, and year on annual tree growth derived using tree-ring records of ten globally distributed forests

Tree rings provide an invaluable long-term record for understanding how climate and other drivers shape tree growth and forest productivity. However, conventional tree-ring analysis methods were not designed to simultaneously account for the effects of climate, tree size, and other drivers on individual growth, which has limited the potential to use tree rings to understand forest productivity, its climate sensitivity, and its global change responses. Here, we develop and apply a new method to simultaneously model non-linear effects of primary climate drivers, reconstructed tree diameter (DBH), and year in generalized least squares models that account for the temporal autocorrelation inherent to each individual tree’s growth. We analyze data from 3811 trees representing 40 species at 10 globally distributed sites, showing that precipitation, temperature, DBH, and calendar year have additively, and often interactively, influenced annual growth over the past 120 years. Growth responses were predominantly positive to precipitation (usually over ≥ 3-month seasonal windows) and negative to temperature (usually over ≤ 3-month seasonal windows), with both included in 78% of top models, and with non-linear responses prevalent (63% of relationships). Climate sensitivity commonly varied with DBH (44% of cases tested). Trends in ring width at small DBH were linked to the light environment under which trees established, but basal area or biomass increments consistently peaked at intermediate DBH and declined thereafter. Accounting for climate and DBH, growth rate declined over time for 92% of species in secondary or disturbed stands, whereas growth trends were mixed in older forests. These trends were largely attributable to stand dynamics as cohorts and stands age, which remain challenging to disentangle from global change drivers. By providing a parsimonious approach for characterizing multiple interacting drivers of tree growth, our method reveals a more complete picture of the factors influencing growth than has previously been possible.

Indiana, Massachusetts, New Mexico, Nebraska, Utah↗
USGS2007

Growth rate differences between resident native brook trout and non-native brown trout

Between species and across season variation in growth was examined by tagging and recapturing individual brook trout Salvelinus fontinalis and brown trout Salmo trutta across seasons in a small stream (West Brook, Massachusetts, U.S.A.). Detailed information on body size and growth are presented to (1) test whether the two species differed in growth within seasons and (2) characterize the seasonal growth patterns for two age classes of each species. Growth differed between species in nearly half of the season- and age-specific comparisons. When growth differed, non-native brown trout grew faster than native brook trout in all but one comparison. Moreover, species differences were most pronounced when overall growth was high during the spring and early summer. These growth differences resulted in size asymmetries that were sustained over the duration of the study. A literature survey also indicated that non-native salmonids typically grow faster than native salmonids when the two occur in sympatry. Taken together, these results suggest that differences in growth are not uncommon for coexisting native and non-native salmonids. ?? 2007 The Authors.

Journal of Fish Biology↗
USGS2010

Vulnerability of white spruce tree growth in interior Alaska in response to climate variability: Dendrochronological, demographic, and experimental perspectives

This paper integrates dendrochronological, demographic, and experimental perspectives to improve understanding of the response of white spruce ( Picea glauca (Moench) Voss) tree growth to climatic variability in interior Alaska. The dendrochronological analyses indicate that climate warming has led to widespread declines in white spruce growth throughout interior Alaska that have become more prevalent during the 20th century. Similarly, demographic studies show that white spruce tree growth is substantially limited by soil moisture availability in both mid- and late-successional stands. Interannual variability in tree growth among stands within a landscape exhibits greater synchrony than does growth of trees that occupy different landscapes, which agrees with dendrochronological findings that the responses depend on landscape position and prevailing climate. In contrast, the results from 18 years of a summer moisture limitation experiment showed that growth in midsuccessional upland stands was unaffected by moisture limitation and that moisture limitation decreased white spruce growth in floodplain stands where it was expected that growth would be less vulnerable because of tree access to river water. Taken together, the evidence from the different perspectives analyzed in this study clearly indicates that white spruce tree growth in interior Alaska is vulnerable to the effects of warming on plant water balance.

Alaska↗
USGS1994

The enigma of oil and gas field growth

Growth in estimates of recovery in discovered fields is an important source of annual additions to United States proved reserves. This paper examines historical field growth and presents estimates of future additions to proved reserves from fields discovered before 1992. Field-level data permitted the sample to be partitioned on the basis of recent field growth patterns into outlier and common field sets, and analyzed separately. The outlier field set accounted for less than 15% of resources, yet grew proportionately six times as much as the common fields. Because the outlier field set contained large old heavy-oil fields and old low-permeability gas fields, its future growth is expected to be particularly sensitive to prices. A lower bound of a range of estimates of futu e growth was calculated by applying monotone growth functions computed from the common field set to all fields. Higher growth estimates were obtained by extrapolating growth of the common field set and assuming the outlier fields would maintain the same share of total growth that occurred from 1978 through 1991. By 2020, the two estimates for additions to reserves from pre-1992 fields are 23 and 32 billion bbl of oil in oil fields and 142 and 195 tcf of gas in gas fields.

American Association of Petroleum Geologists Bulle↗
USGS2017

Linking functional response and bioenergetics to estimate juvenile salmon growth in a reservoir food web

Juvenile salmon ( Oncorhynchus spp.) use of reservoir food webs is understudied. We examined the feeding behavior of subyearling Chinook salmon ( O . tshawytscha ) and its relation to growth by estimating the functional response of juvenile salmon to changes in the density of Daphnia , an important component of reservoir food webs. We then estimated salmon growth across a broad range of water temperatures and daily rations of two primary prey, Daphnia and juvenile American shad ( Alosa sapidissima ) using a bioenergetics model. Laboratory feeding experiments yielded a Type-II functional response curve: C = 29.858 P *(4.271 + P ) -1 indicating that salmon consumption ( C ) of Daphnia was not affected until Daphnia densities ( P ) were < 30 · L -1 . Past field studies documented Daphnia densities in lower Columbia River reservoirs of < 3 · L -1 in July but as high as 40 · L -1 in August. Bioenergetics modeling indicated that subyearlings could not achieve positive growth above 22°C regardless of prey type or consumption rate. When feeding on Daphnia , subyearlings could not achieve positive growth above 20°C (water temperatures they commonly encounter in the lower Columbia River during summer). At 16–18°C, subyearlings had to consume about 27,000 Daphnia · day -1 to achieve positive growth. However, when feeding on juvenile American shad, subyearlings had to consume 20 shad · day -1 at 16–18°C, or at least 25 shad · day -1 at 20°C to achieve positive growth. Using empirical consumption rates and water temperatures from summer 2013, subyearlings exhibited negative growth during July (-0.23 to -0.29 g · d -1 ) and August (-0.05 to -0.07 g · d -1 ). By switching prey from Daphnia to juvenile shad which have a higher energy density, subyearlings can partially compensate for the effects of higher water temperatures they experience in the lower Columbia River during summer. However, achieving positive growth as piscivores requires subyearlings to feed at higher consumption rates than they exhibited empirically. While our results indicate compromised growth in reservoir habitats, the long-term repercussions to salmon populations in the Columbia River Basin are unknown.

PLoS ONE↗
USGS1947

Age and growth of the kiyi, Leucichthys kiyi Koelz, in Lake Michigan

Ages were determined and individual growth histories were calculated from the examination and measurement of the scales of 1,649 kiyis captured at seven localities in Lake Michigan in 1931 and 1932. The numbers of individuals employed for the investigation of other phases of the life history (such as length-frequency distributions, length-weight relationship, and sex ratio) varied according to the amount of data available or required. Age-group IV was dominant in the 1931 collections from Racine, Port Washington, and Kewaunee, Wisconsin, and age-group V dominated the 1932 samples from the Fox Islands and from three localities southward of Manistique, Michigan. A trend was noticeable toward an increase in average age from south to north. Among the explanations suggested for the observed differences in age composition were: Variation with latitude in the natural span of life; differences in fishing intensity; fluctuations in the strength of year classes (to account possibly for the shift in the dominant age group from 1931 to 1932). The oldest male kiyi belonged to the VII group and the oldest female was a member of the X group. The possible distorting effects of such factors as gear selection traceable to differences in the mesh sizes of nets fished in 1931 and 1932, selection by nets on the basis of the condition (K) of the fish, and local variations in fishing intensity and hence in the selective destruction of rapidly growing individuals in the fishery were held to be sufficiently great to render doubtful the significance of most of the observed local differences in growth rate. Kiyis from all samples were combined to determine the general growth in length. The growth in weight of the Fox Islands fish, however, was considered separately as these fish were consistently lighter than kiyis of corresponding length from other localities. The Lake Michigan kiyi grows slowly, with the females growing slightly more rapidly than the males. The grand average calculated lengths indicated, for example, that the females did not attain a total length of 10 inches until the fifth year of life or the males until the sixth. Similarly, the calculated weight of 4 ounces was not reached until the fifth or sixth year (with the actual time varying with sex and locality). The season's growth of the kiyi probably begins sometime in May and most or all of the growth is completed by the end of August. The calculated lengths of the age groups exhibited large discrepancies that differed from “Lee's phenomenon” as ordinarily observed in that the data for the later rather than the earlier years of life were affected most severely. Chief among the factors held responsible for these discrepancies were gear selection and the selective destruction of the more rapidly growing individuals in the fishery. Errors inherent in the (direct-proportion) method of computing growth from scale measurements were considered to have been unimportant. The Lake Michigan kiyi exhibits growth compensation–the tendency for the smaller of the young fish to have the more rapid growth in the later years of life. Comparisons with the average lengths and weights of the age groups of the Lake Ontario kiyi given by Pritchard (1931) indicated the Lake Michigan fish to be the larger at the earlier ages (age-groups II and III) and the smaller at the later ages (age-groups IV to VI). The length-frequency distributions of the age groups exhibited extensive overlap. As many as eight age groups were represented in a single centimeter interval of length. The length frequencies and average lengths of all fish collected, arranged according to the mesh sizes of the gill nets by which they were captured, revealed that the selective action of these nets in the taking of kiyis was much more obvious in the numbers of fish in the catch than in their average size. As an illustration, in 1930–1931, the 2 3/4-inch mesh nets took fish that were only 0.1 inch longer than those in 2 1/2-inch meshes but captured less than one fourth as many. Gill nets fished in northern Lake Michigan in 1932 captured kiyis that averaged 0.2 to 0.4 inch longer than those taken in the same meshes in southern Lake Michigan in 1930–1931. Because of the more slender form of kiyis from the northeastern island region of Lake Michigan, data on the general length weight relationship were compiled separately for fish of that area and for those of the great central basins of the lake. In both regions the weight increased to a power slightly greater than the cube of the length. Available information on condition indicated that the coefficient (K) was higher in August and early September than in May, June, and July. Condition declined from early September to October and early November–the latter period the time of most active spawning. Spawning itself was accompanied by an additional loss of about 12 per cent of the body weight of females and of somewhat less than 2 per cent of the weight of males. Analysis of the variations of K within a group that was homogeneous with respect to age, sex, maturity, and time of collection revealed that a net of a particular mesh size tends to take the heavier of the shorter fish and the lighter of the longer fish within its range of effectiveness. Among fish of the same length the values of K tended to increase with increase in the mesh size of the nets employed for their capture. Practically all fish in the samples were mature (only 11 immature in more than 6,000). These “immature” fish were probably “non-functional” since all of them approached or exceeded the average length of the mature kiyis. Females were strongly predominant in the collections at all seasons but were relatively more plentiful during the summer (90 per cent of the total) than during the spawning period (75 per cent). Possible factors contributing to this predominance of females and to the change in the sex ratio at the spawning season were discussed. A decrease in the relative abundance of males with increase in age appears to be characteristic of the kiyi. This decrease indicates a differential mortality of th sexes (greater relative destruction of males in the spawning period when they are unusually abundant or a greater natural mortality rate for the males). Current fishery regulations on mesh size and closed seasons afford the kiyi good protection but offer no guarantee against depletion from too intensive fishing.

Transactions of the American Fisheries Society↗
USGS1997

Age and growth of alewives in the changing pelagia of Lake Ontario, 1978-1992

We documented the age and growth of alewives Alosa pseudoharenqus in Lake Ontario during 1978-1992 and determined if growth was affected by intraspecific competition for epilimnetic zooplankton, lake temperature, or demand of salmonine piscivores for prey. Ages of juvenile alewives were determined from scales during 1978-1983, and ages of juvenile and adult alewives were determined from otoliths during 1984-1992. Indices of abundance for alewives were calculated from spring bottom trawl catches in 1978-1992; zooplankton density and epilimnetic temperature were monitored at two stations during 1981-1991; and salmonine demand each year during 1978-1992 was calculated with a simulation model. Although we encountered 11-year-old alewives, few fish lived longer than 7 years, and most fish in the population were younger than 6 years. Mean sizes at ages 1, 2, and 3 in spring averaged 93 mm (5.1 g), 133 mm (17 g), and 149 mm (22 g), but from age 3 to age 8, mean size increased by only 5-7 mm and 2-3 g per year. Female alewives lived longer than male alewives and were always longer than male alewives at age 4 and older. Epilimnetic temperatures were suitable for rapid growth of juvenile alewives each year. Lake temperature had the potential to affect growth of adults but adult growth was not correlated with temperature suitability indices perhaps because temperature regimes differed among lake regions and alewives were mobile. Growth of alewives was not correlated with salmonine demand for prey. Competition for zooplankton among the two youngest alewife cohorts affected growth of age-1 alewives. Zooplankton density declined sharply in 1986, and should it decline again, growth of age-1 alewives will slow, unless numbers of age-0 alewives fall. Whether growth of age-1 fish declines or numbers of age-0 fish fall, the result of another decline in zooplankton density will be a reduction in the production of alewives needed to support piscivores.

Transactions of the American Fisheries Society↗
USGS2011

Interactions between slimy sculpin and trout: Slimy sculpin growth and diet in relation to native and nonnative trout

To investigate whether introductions of nonnative trout affect growth and diet of nongame fish in small streams, we designed a field experiment to examine interactions between slimy sculpin Cottus cognatus and native brook trout Salvelinus fontinalis or nonnative brown trout Salmo trutta. We hypothesized that brown trout would compete with and reduce growth of slimy sculpin. We expected no change in slimy sculpin growth in treatments with brook trout because the two species co-occur in their native range and thus may have evolved methods to partition resources and decrease competitive interactions. Enclosures (1 m2) were stocked with (1) juvenile brown trout and slimy sculpin, (2) juvenile brook trout and slimy sculpin, or (3) slimy sculpin alone (control). Fish were stocked at three densities to examine intraspecific versus interspecific competition. Replicates of each treatment were placed in riffles in Valley Creek, Minnesota, and six experimental trials were conducted over three summers (2002-2004). Brown trout presence was associated with reduced growth of large slimy sculpin in enclosures, whereas brook trout presence produced no change in slimy sculpin growth; these effects did not depend on fish density. Brown trout or brook trout presence was not associated with shifts in the diets of slimy sculpin, indicating that reduced slimy sculpin growth in the presence of brown trout was not due to prey selection or prey availability changes. Our research suggests that effects on growth of slimy sculpin in Valley Creek differ between introduced brown trout and native brook trout; however, the mechanisms underlying changes in slimy sculpin growth are unclear. Although brook trout and brown trout appear to fill similar ecological roles in small, coldwater streams, brown trout may negatively impact growth of nongame fish. ?? Copyright by the American Fisheries Society 2007.

Transactions of the American Fisheries Society↗
USGS2002

On geological interpretations of crystal size distributions: Constant vs. proportionate growth

Geological interpretations of crystal size distributions (CSDs) depend on understanding the crystal growth laws that generated the distributions. Most descriptions of crystal growth, including a population-balance modeling equation that is widely used in petrology, assume that crystal growth rates at any particular time are identical for all crystals, and, therefore, independent of crystal size. This type of growth under constant conditions can be modeled by adding a constant length to the diameter of each crystal for each time step. This growth equation is unlikely to be correct for most mineral systems because it neither generates nor maintains the shapes of lognormal CSDs, which are among the most common types of CSDs observed in rocks. In an alternative approach, size-dependent (proportionate) growth is modeled approximately by multiplying the size of each crystal by a factor, an operation that maintains CSD shape and variance, and which is in accord with calcite growth experiments. The latter growth law can be obtained during supply controlled growth using a modified version of the Law of Proportionate Effect (LPE), an equation that simulates the reaction path followed by a CSD shape as mean size increases.

American Mineralogist↗
USGS2019

Early-warning signals of individual tree mortality based on annual radial growth

Tree mortality is a key driver of forest dynamics and its occurrence is projected to increase in the future due to climate change. Despite recent advances in our understanding of the physiological mechanisms leading to death, we still lack robust indicators of mortality risk that could be applied at the individual tree scale. Here, we build on a previous contribution exploring the differences in growth level between trees that died and survived a given mortality event to assess whether changes in temporal autocorrelation, variance, and synchrony in time-series of annual radial growth data can be used as early warning signals of mortality risk. Taking advantage of a unique global ring-width database of 3065 dead trees and 4389 living trees growing together at 198 sites (belonging to 36 gymnosperm and angiosperm species), we analyzed temporal changes in autocorrelation, variance, and synchrony before tree death (diachronic analysis), and also compared these metrics between trees that died and trees that survived a given mortality event (synchronic analysis). Changes in autocorrelation were a poor indicator of mortality risk. However, we found a gradual increase in inter-annual growth variability and a decrease in growth synchrony in the last ∼20 years before mortality of gymnosperms, irrespective of the cause of mortality. These changes could be associated with drought-induced alterations in carbon economy and allocation patterns. In angiosperms, we did not find any consistent changes in any metric. Such lack of any signal might be explained by the relatively high capacity of angiosperms to recover after a stress-induced growth decline. Our analysis provides a robust method for estimating early-warning signals of tree mortality based on annual growth data. In addition to the frequently reported decrease in growth rates, an increase in inter-annual growth variability and a decrease in growth synchrony may be powerful predictors of gymnosperm mortality risk, but not necessarily so for angiosperms.

Frontiers in Plant Science↗
USGS1999

Aspects of chick growth in Gull-billed Terns in coastal Virginia

Because of concerns about apparent population declines and low productivity of Gull-billed Terns (Sterna nilotica) along the coast of Virginia, we investigated whether food limitations may result in retarded growth rates of young. Several colonies of Gull-billed Terns were monitored from May to July each year from 1994 to 1996 on both sandy barrier islands and marsh/shellpile islands in coastal Virginia. Nests were visited one to three times a week to monitor clutch size and hatching success, and enclosures were installed around selected nests to monitor chick growth from hatching to at least two weeks of age. When comparing chick growth, we found significant year, habitat and hatch order effects. Chicks from marsh shellpiles had higher mass and culmen growth rates than did those from barrier islands, and first-hatched (A) chicks had significantly higher culmen growth rates than did second-hatched (B) chicks. Year effects were only found for mass growth rates. Growth rates of Gull- billed Terns in these Virginia colonies seem to be low relative to those of six other North American tern species from other geographic areas. These findings suggest that growth rates of young Gull-billed Terns, as well as other reproductive parameters, need to be examined in detail in other coastal areas such as Texas, where the species is more abundant, to determine whether our growth results are species- or region-specific.

Waterbirds↗
USGS2011

Growth rate variation among passerine species in tropical and temperate sites: an antagonistic interaction between parental food provisioning and nest predation risk

Causes of interspecific variation in growth rates within and among geographic regions remain poorly understood. Passerine birds represent an intriguing case because differing theories yield the possibility of an antagonistic interaction between nest predation risk and food delivery rates on evolution of growth rates. We test this possibility among 64 Passerine species studied on three continents, including tropical and north and south temperate latitudes. Growth rates increased strongly with nestling predation rates within, but not between, sites. The importance of nest predation was further emphasized by revealing hidden allometric scaling effects. Nestling predation risk also was associated with reduced total feeding rates and per-nestling feeding rates within each site. Consequently, faster growth rates were associated with decreased per-nestling food delivery rates across species, both within and among regions. These relationships suggest that Passerines can evolve growth strategies in response to predation risk whereby food resources are not the primary limit on growth rate differences among species. In contrast, reaction norms of growth rate relative to brood size suggest that food may limit growth rates within species in temperate, but not tropical, regions. Results here provide new insight into evolution of growth strategies relative to predation risk and food within and among species.

Evolution↗
USGS1988

Phytoplankton growth rates in a light-limited environment, San Francisco Bay

Phytoplankton cells reside in a turbulent medium partitioned into an upper photic zone that sustains photosynthesis, and a lower aphotic zone that does not. In estuaries, vertical mixing rates between these 2 zones can be rapid (< 1 generation time) because of tidal stirring and because the mixing depth is generally shallow. Moreover, the photic depth is characteristically shallow in estuaries because of the high seston concentrations that typify these systems (e.g. Cloern 1987). Hence the mean light exposure of phytoplankton cells, and their rates of photosynthesis and growth in estuaries, should be related to the ratio of photic depth Z p to mixing Z m , (defined as either the water column depth, or the surface layer depth in a stratified estuary). Grobbelar (1985) has measured phytoplankton production in turbid waters and used the ratio Z p :Z m as a simple index to quantify the degree of light limitation. Harris and his colleagues have examined in detail the importance of the Z p :Z m ratio in lakes for influencing variability of phytoplankton production and photosynthetic parameters (Harris et al. 1980), and variability of species composition both temporally (Harris & Piccinin 1980) and spatially (Haffner et al. 1980). Phytoplankton growth rates have only rarely been measured in estuaries (Malone 1977, Furnas 1982, Harding et al. 1986) where cycling rates between the photic and aphotic zones can be much faster than in lakes or the open ocean. This study was motivated by the need for quantitative measures of phytoplankton population growth rate in an estuarine environment, and was designed around the presumption that growth rates can be related empirically to light exposure. We conducted the study in San Francisco Bay (California, USA), which has large horizontal gradients in light availability (Z p :Z m ) typical of many coastal plain estuaries, and nutrient concentrations that often exceed those presumed to limit phytoplankton growth (Cloern et al. 1985). We tested the hypothesis that light availability is the primary control of phytoplankton growth, and that previous estimates of growth rate based on the ratio of productivity to biomass (Cloern et al. 1985) are realistic. Specifically, we wanted to verify that growth rate varies spatially along horizontal gradients of light availability indexed as Z p :Z m , such that phytoplankton turnover rate is rapid in shallow clear areas (high Z p :Z m ) and slow in deep turbid areas (low Z p :Z m ). We used an in situ incubation technique which simulated vertical mixing, and measured both changes in cell number and carbon production as independent estimates of growth rate across a range of Z p :Z m ratios.

California↗
USGS2021

Increased growth rates of stream salamanders following forest harvesting

Timber harvesting can influence headwater streams by altering stream productivity, with cascading effects on the food web and predators within, including stream salamanders. Although studies have examined shifts in salamander occupancy or abundance following timber harvest, few examine sublethal effects such as changes in growth and demography. To examine the effect of upland harvesting on growth of the stream-associated Ouachita dusky salamander ( Desmognathus brimleyorum ), we used capture–mark–recapture over three years at three headwater streams embedded in intensely managed pine forests in west-central Arkansas. The pine stands surrounding two of the streams were harvested, with retention of a 14- and 21-m-wide forested stream buffer on each side of the stream, whereas the third stream was an unharvested control. At the two treatment sites, measurements of newly metamorphosed salamanders were on average 4.0 and 5.7 mm larger post-harvest compared with pre-harvest. We next assessed the influence of timber harvest on growth of post-metamorphic salamanders with a hierarchical von Bertalanffy growth model that included an effect of harvest on growth rate. Using measurements from 839 individual D . brimleyorum recaptured between 1 and 6 times (total captures, n = 1229), we found growth rates to be 40% higher post-harvest. Our study is among the first to examine responses of individual stream salamanders to timber harvesting, and we discuss mechanisms that may be responsible for observed shifts in growth. Our results suggest timber harvest that includes retention of a riparian buffer (i.e., streamside management zone) may have short-term positive effects on juvenile stream salamander growth, potentially offsetting negative sublethal effects associated with harvest.

Arkansas↗
USGS2017

The estimation of growth dynamics for Pomacea maculata from hatchling to adult

Pomacea maculata is a relatively new invasive species to the Gulf Coast region and potentially threatens local agriculture (rice) and ecosystems (aquatic vegetation). The population dynamics of P. maculata have largely been unquantified, and therefore, scientists and field-workers are ill-equipped to accurately project population sizes and the resulting impact of this species. We studied the growth of P. maculata ranging in weights from 6 to 105 g, identifying the sex of the animals when possible. Our studied population had a 4:9 male:female sex ratio. We present the findings from initial analysis of the individual growth data of males and females, from which it was apparent that females were generally larger than males and that small snails grew faster than larger snails. Since efforts to characterize the male and female growth rates from individual data do not yield statistically supported estimates, we present the estimation of several parameterized growth rate functions within a population-level mathematical model. We provide a comparison of the results using these various growth functions and discuss which best characterizes the dynamics of our observed population. We conclude that both males and females exhibit biphasic growth rates, and thus, their growth is size-dependent. Further, our results suggest that there are notable differences between males and females that are important to take into consideration in order to accurately model this species' population dynamics. Lastly, we include preliminary analyses of ongoing experiments to provide initial estimates of growth in the earliest life stages (hatchling to ≈6 g).

Ecosphere↗
USGS2022

Mark-recapture models accurately predict growth trajectories of known-age Muskellunge in Green Bay, Lake Michigan

Length-at-age data are commonly used to describe growth of fish, and obtaining these data typically involves estimating ages from calcified structures (e.g., fin spines or rays, otoliths, or cleithra). Verifying the accuracy of age and growth estimates for long-lived fish is often difficult because known-age fish are not available for all ages in a population. Mark–recapture methods offer nonlethal alternatives for estimating growth of fish that do not require age data. However, few studies have compared growth trajectories estimated from mark–recapture data with trajectories estimated using the standard von Bertalanffy growth function (VBGF) incorporating length-at-age data from known-age fish. We used a robust data set of Muskellunge Esox masquinongy sampled from Green Bay, Lake Michigan, during 1990–2018 to compare growth trajectories estimated from three mark–recapture models and a VBGF fitted to length-at-age data from known-age individuals. Growth trajectories estimated with mark–recapture models were similar to trajectories estimated with a VBGF using known-age fish. Our results suggest that using recapture of tagged fish provides a viable alternative for describing Muskellunge growth trajectories compared with using ages estimated from calcified structures, where incorrect age estimates represent an additional source of error.

Wisconsin↗
USGS2019

Fish growth changes over time in a Midwestern U.S. lake

Growth of Walleyes Sander vitreus, Yellow Bass Morone mississippiensis, Common Carp Cyprinus carpio, and Black Bullheads Ameiurus melas was assessed in Clear Lake, Iowa, over several decades and in relation to environmental variables. Growth of Common Carp was positively correlated with phytoplankton concentration. Recent Black Bullhead growth was faster than in the 1950s and 1990s, which may be a consequence of their recent decline in abundance. Growth of Common Carp and Yellow Bass was faster in the 1940s than in more recent time periods. Relative to their entire range, Common Carp first‐year growth was below average, whereas length at later ages was above average. Walleye relative growth showed a similar pattern. The large changes in growth over several decades suggest that as the Clear Lake ecosystem continues to change, growth rates of its important fish species are also likely to continue changing.

Transactions of the American Fisheries Society↗