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At least 235 records · Page 13Linked to original sources

Age and growth of a native, lightly exploited population of Coregonus clupeaformis (Lake Whitefish) in a small natural lake in Maine

We assessed annual growth of Coregonus clupeaformis (Lake Whitefish) from a natural, lightly exploited population in a small lake in northern Maine using observed and back-calculated length-at-age data. We sampled Lake Whitefish from Clear Lake, ME, with gill nets and extracted otoliths from 57 fish. We incorporated age-at-length data into a von Bertalanffy growth function, which we employed to model growth trajectories from individual fish. We used these estimates to evaluate length-at-age variability within this population. Ages for Lake Whitefish varied from 8 y to 30 y. Among all fish, we characterized incremental growth by an average-growth coefficient of K = 0.156 and an estimated L∞ of 484 mm. The oldest individuals demonstrated the slowest incremental growth (K = 0.106) when compared to younger cohorts (K = 0.218). We observed an inverse relationship between L∞ and K and the estimated age-at-capture (R2 = 0.178 and 0.723, respectively), which suggests relatively slow growth and a smaller maximum size for the longest living members of the population. Our estimated parameters serve as a reference to inform management of populations of Lake Whitefish.

Maine↗

Estimating age from recapture data: Integrating incremental growth measures with ancillary data to infer age-at-length

Estimating the age of individuals in wild populations can be of fundamental importance for answering ecological questions, modeling population demographics, and managing exploited or threatened species. Significant effort has been devoted to determining age through the use of growth annuli, secondary physical characteristics related to age, and growth models. Many species, however, either do not exhibit physical characteristics useful for independent age validation or are too rare to justify sacrificing a large number of individuals to establish the relationship between size and age. Length‐at‐age models are well represented in the fisheries and other wildlife management literature. Many of these models overlook variation in growth rates of individuals and consider growth parameters as population parameters. More recent models have taken advantage of hierarchical structuring of parameters and Bayesian inference methods to allow for variation among individuals as functions of environmental covariates or individual‐specific random effects. Here, we describe hierarchical models in which growth curves vary as individual‐specific stochastic processes, and we show how these models can be fit using capture–recapture data for animals of unknown age along with data for animals of known age. We combine these independent data sources in a Bayesian analysis, distinguishing natural variation (among and within individuals) from measurement error. We illustrate using data for African dwarf crocodiles, comparing von Bertalanffy and logistic growth models. The analysis provides the means of predicting crocodile age, given a single measurement of head length. The von Bertalanffy was much better supported than the logistic growth model and predicted that dwarf crocodiles grow from 19.4 cm total length at birth to 32.9 cm in the first year and 45.3 cm by the end of their second year. Based on the minimum size of females observed with hatchlings, reproductive maturity was estimated to be at nine years. These size benchmarks are believed to represent thresholds for important demographic parameters; improved estimates of age, therefore, will increase the precision of population projection models. The modeling approach that we present can be applied to other species and offers significant advantages when multiple sources of data are available and traditional aging techniques are not practical.

Loango National Park↗

Effects of stream enclosures on drifting invertebrates and fish growth

Stream ecologists often use enclosure experiments to investigate predator-prey interactions and competition within and among fish species. The design of enclosures, manipulation of species densities, and method of replication may influence experimental results. We designed an experiment with enclosure cages (1 m2, 6-mm mesh) to examine the relative influence of fish size, density, and prey availability on growth of brown trout (Salmo trutta), brook trout (Salvelinus fontinalis), and slimy sculpin (Cottus cognatus) within enclosures in Valley Creek, Minnesota. In addition, we examined water flow and invertebrate drift entering enclosures and in open riffles to investigate whether enclosures reduced the supply of invertebrate prey. Growth of small (age-0) brook and brown trout was not influenced by fish density, but growth of larger (age-1) trout generally decreased as density increased. Sculpin growth was not related to fish size or density, but increased with mean size of invertebrates in the drift. Enclosures reduced water flow and tended to reduce invertebrate drift rate, although total drift rate (ind./min), total drift density (ind./m3), and mean size of invertebrates were not significantly different inside enclosures compared to adjacent stream riffles. Enclosures had no effect on drift rate or size of Gammarus pseudolimnaeus, the main prey item for trout and sculpin in Valley Creek. Overall, our analyses indicated that reductions of prey availability by enclosures did not influence fish growth. Trout growth may have been limited at larger sizes and densities because of increased activity costs of establishing and defending territories, whereas sculpin growth was related to availability of large prey, a factor not influenced by enclosures. ?? 2006 by The North American Benthological Society.

Journal of the North American Benthological Societ↗

Growth and invasive potential of Sapium sebiferum (Euphorbiaceae) within the coastal prairie region: the effects of soil and moisture regime

The introduced tree Sapium sebiferum (Euphorbiaceae) is considered a serious threat to the preservation of the coastal prairie region of Louisiana and Texas, although it is currently uncommon in the western part of the region. The objective of this study was to evaluate the potential effects of location, soils, and available moisture on the growth and survival of S. sebiferum in coastal prairie. In a field experiment, S. sebiferum mortality was significantly greater at a western site than at central and eastern sites. The greatest mortality and least growth of surviving plants occurred on a soil from the western region, regardless of site. A greenhouse study also found that S. sebiferum growth was lowest on the western soil. Watering frequency significantly affected S. sebiferum growth, except on the western soil. Sapium sebiferum growth responded to both nitrogen and phosphorum additions for all soils. Soil analyses revealed the highest sand, sodium, and phosphorus contents, and much higher electrical conductivity in the western soil. It is concluded that the soil examined from the western region is unfavorable for S. sebiferum growth, though not to the extent to preclude S. sebiferum completely. Evidence suggests that soil salinity may be the primary cause of the poor S. sebiferum growth at the western site.

Louisiana, Texas↗

Evaluation of transmitter attachment techniques on growth of wild turkey poults

We compared the effects on growth of backpack-mounted and surgically implanted radiotransmitters used as marking techniques in studies of wild turkey ( Meleagris gallopavo ) poult survival. We applied repeated-measures analysis of variance (ANOVA) and Bayesian analysis to evaluate the null hypothesis that marking technique did not affect growth. Growth in body mass was similar among treatment groups. We did, however, find differences in wing-growth rates among treatment groups. The control group had the highest wing-growth rate, the backpack group had the lowest growth rate, and the surgical implant group was intermediate. Latex backpack harnesses also caused physical developmental problems that would have negatively biased wild poult survival estimates in the field. Surgically implanted transmitters affected wing growth less than the backpack harnesses and are therefore recommended for attaching transmitters to wild turkey poults.

Journal of Wildlife Management↗

Deducing growth mechanisms for minerals from the shapes of crystal size distributions

Crystal size distributions (CSDs) of natural and synthetic samples are observed to have several distinct and different shapes. We have simulated these CSDs using three simple equations: the Law of Proportionate Effect (LPE), a mass balance equation, and equations for Ostwald ripening. The following crystal growth mechanisms are simulated using these equations and their modifications: (1) continuous nucleation and growth in an open system, during which crystals nucleate at either a constant, decaying, or accelerating nucleation rate, and then grow according to the LPE; (2) surface-controlled growth in an open system, during which crystals grow with an essentially unlimited supply of nutrients according to the LPE; (3) supply-controlled growth in an open system, during which crystals grow with a specified, limited supply of nutrients according to the LPE; (4) supply- or surface-controlled Ostwald ripening in a closed system, during which the relative rate of crystal dissolution and growth is controlled by differences in specific surface area and by diffusion rate; and (5) supply-controlled random ripening in a closed system, during which the rate of crystal dissolution and growth is random with respect to specific surface area. Each of these mechanisms affects the shapes of CSDs. For example, mechanism (1) above with a constant nucleation rate yields asymptotically-shaped CSDs for which the variance of the natural logarithms of the crystal sizes (??2) increases exponentially with the mean of the natural logarithms of the sizes (??). Mechanism (2) yields lognormally-shaped CSDs, for which ??2 increases linearly with ??, whereas mechanisms (3) and (5) do not change the shapes of CSDs, with ??2 remaining constant with increasing ??. During supply-controlled Ostwald ripening (4), initial lognormally-shaped CSDs become more symmetric, with ??2 decreasing with increasing ??. Thus, crystal growth mechanisms often can be deduced by noting trends in ?? versus ??2 of CSDs for a series of related samples.

American Journal of Science↗

Differential effects of temperature and salinity on growth and mortality of oysters (Crassostrea virginica) in Barataria Bay and Breton Sound, Louisiana

Temperature and salinity and their interaction exert a major control on the life cycle of the eastern oyster (Crassostrea virginica), affecting reproduction, development, growth, and mortality. Quantifying specific temperature and salinity relationships on oyster growth and mortality has however proven difficult, with data suggesting potentially region-specific responses. Legacy and recent data from field tray studies from public oyster grounds in Barataria Bay and Breton Sound were used to estimate growth and mortality rates as a function of temperature and salinity. Previous studies conducted in Barataria Bay and Breton Sound reported differences in growth and mortality between the basins. In the present study, environmental conditions were synchronized to compare growth and mortality between basins at similar combinations of temperature and salinity. Results indicate that when temperature and salinity are the same (synchronized), seasonal oyster growth and mortality rates still differ between Barataria Bay and Breton Sound. Given the same salinity and temperature conditions, differences in growth and mortality rates between estuaries may persist due to differences in other environmental conditions (i.e., food quality and composition, hydrology, site history, salinity variation) or localized genetic adaptations to environmental conditions.

Lousianna↗

Growth and mortality of coral transplants (Pocillopora damicornis) along a range of sediment influence in Maui, Hawai'i

Fragments of the lace coral Pocillopora damicornis (Linnaeus, 1758) were transplanted to four sites on the south-central coast of Maui, Hawai'i, to examine coral growth over a range of expected sediment influence. Corals remained in situ for 11 months and were recovered seasonally for growth measurements using the buoyant weight technique. Average sediment trap accumulation rates ranged from 11 to 490 mg cm-2 day-1 and were greater at the wave-exposed reef site than at the protected harbor sites. Coral growth was highest at the donor site and was higher in the summer than in the winter. A stepwise linear regression found significant effects of sediment trap accumulation and light on growth rates, but the partial correlation coefficients suggest that these factors may be only secondary controls on growth. This study did not show a clear link between coral growth and sediment load. This result may be due, in part, to covariation of sediment load with wave exposure and the inability of trap accumulation rates to integrate all sediment effects (e.g., turbidity) that can affect coral growth. ?? 2008 by University of Hawai'i Press. All rights reserved.

Pacific Science↗

Growth history of oil reserves in major California oil fields during the twentieth century

Oil reserves in 12 of California's 52 giant fields (fields with estimated recovery > 100 million barrels of oil) have continued to appreciate well past the age range at which most fields cease to show significant increases in ultimate recovery. Most of these fields were discovered between 1890 and 1920 and grew to volumes greater than 500 million barrels in their first two decades. Growth of reserves in these fields accelerated in th e1950s and 1960s and is mostly explained by application of secondary and tertiary recovery technicques, primarily waterflooding and thermal recovery. The remaining three-fourths of California's giant fields show a pattern of growth in which fields cease to grow significantly by 20-30 years following recovery. virtually all of these fields have estimated ultimate recoveries less than about 500 million barrels and most are in the 100-200 million barrel range. Three of six offshore giant fields, all discovered between 1966 and 1981, have shown decreases in their estimated ultimate sizes within about the first decade after production began, presumably because production volumes ailed to match initial projections. The data suggest that: 1. Only fields that attain an estimated ultimate size of several hundred million barrels shortly after discovery and have geologic characterisics that make them suceptible to advanced recovery techniques are likely to show substantial late growth. 2. Offshore fields are less likely to show significant growth, probably because projections based on modern seismic reflection and reservoir test data are unlikely to underestimate the volume of oil in the field. 3. Secondary and tertiary recovery programs rather than field extensions or new pool discoveries are responsible for most of the significant growth of reserves in California. 4. field size data collected ove rmany decades provide a more comprehensive context for inferring reasons for reserve appreciation than shorter data series such as the Oil and Gas Integrated Field file (OGIFF) from the U.S. Department of Energy's Energy Information Administration (EIA). 5. Efforts to project future growth in California fields, and perhaps fields in other regions, should focus on evaulating the potential for enhanced recovery in fields with current estimated ultimate recoveries of about 250-500 million barrels. 6. By analogy with oil, attempts to project growth in gas reservoirs, in California and perhaps elsewhere, should focus on larger fields with lower permeability reservoirs where advances in recovery technology, such as perhaps horizontal drilling, are more likely to add substantial reserves.

Bulletin↗

User's Guide to Galoper: A Program for Simulating the Shapes of Crystal Size Distributions from Growth Mechanisms - and Associated Programs

GALOPER is a computer program that simulates the shapes of crystal size distributions (CSDs) from crystal growth mechanisms. This manual describes how to use the program. The theory for the program's operation has been described previously (Eberl, Drits, and Srodon, 1998). CSDs that can be simulated using GALOPER include those that result from growth mechanisms operating in the open system, such as constant-rate nucleation and growth, nucleation with a decaying nucleation rate and growth, surface-controlled growth, supply-controlled growth, and constant-rate and random growth; and those that result from mechanisms operating in the closed system such as Ostwald ripening, random ripening, and crystal coalescence. In addition, CSDs for two types weathering reactions can be simulated. The operation of associated programs also is described, including two statistical programs used for comparing calculated with measured CSDs, a program used for calculating lognormal CSDs, and a program for arranging measured crystal sizes into size groupings (bins).

Open-File Report↗

Reserve Growth of Alberta Oil Pools

This Open-File Report is based on a presentation delivered at the Fourth U.S. Geological Survey Workshop on Reserve Growth on March 10-11, 2008. It summarizes the results of a study of reserve growth of oil pools in Alberta Province, Canada. The study is part of a larger effort involving similar studies of fields in other important petroleum provinces around the world, with the overall objective of gaining a better understanding of reserve growth in fields with different geologic/reservoir parameters and different operating environments. The goals of the study were to: 1. Evaluate historical oil reserve data and assess reserve growth. 2. Develop reserve growth models/functions to help forecast hydrocarbon volumes. 3. Study reserve growth sensitivity to various parameters ? for example, pool size, porosity, oil gravity, and lithology. 4. Compare reserve growth in oil pools/fields of Alberta provinces with those from other large petroleum provinces.

Open-File Report↗

Reserve growth during financial volatility in a technologically challenging world

Reserve growth (growth-to-known) is the addition of oil and gas quantities to reported proved or proved-plus-probable reserves in discovered fields. The amount of reserve growth fluctuates through time with prevailing economic and technological conditions. Most reserve additions are the result of investment in field operations and in development technology. These investments can be justified by higher prices of oil and gas, the desire to maintain cash flow, and by greater recovery efficiency in well established fields. The price/cost ratio affects decisions for field abandonment and (or) implementation of improved recovery methods. Although small- to medium-size fields might show higher percentages of reserve growth, a relatively few giant fields contribute most volumetric reserve growth, indicating that companies may prefer to invest in existing fields with low geologic and production risk and an established infrastructure in order to increase their price/cost relationship. Whereas many previous estimates of reserve growth were based on past trends of reported reserves, future reserve growth is expected to be greatly affected by financial volatility and fluctuating economic and technological conditions.

Open-File Report↗

U.S. Geological Survey assessment of reserve growth outside of the United States

The U.S. Geological Survey estimated volumes of potential additions to oil and gas reserves for the United States by reserve growth in discovered accumulations. These volumes were derived by using a new methodology developed by the U.S. Geological Survey and reviewed by the American Association of Petroleum Geologists Committee on Resource Evaluation. This methodology was used to assess reserve growth in individual accumulations (reservoirs, groups of reservoirs, or fields). Selected, large, well-studied, conventional accumulations in the United States that are estimated to contribute most to reserve growth were assessed using analysis of geology and engineering practices. Potential additions to oil and gas reserves for large, discovered, conventional accumulations outside of the United States due to reserve growth were assessed using the U.S. accumulations as analogs. Potential oil and gas volumes were assumed to be added to proven plus probable reserves. The U.S. Geological Survey estimated volumes of technically recoverable, conventional petroleum resources resulting from reserve growth for discovered fields outside the United States that have reported in-place oil and gas volumes of 500 million barrels of oil equivalent or greater. The mean volumes of reserve growth were estimated at 665 billion barrels of crude oil; 1,429 trillion cubic feet of natural gas; and 16 billion barrels of natural gas liquids. These volumes constitute a significant portion of the world’s oil and gas resources and represent the potential future growth of current global reserves over time based on better assessment methodology, new technologies, and greater understanding of reservoirs.

Scientific Investigations Report↗

Using Gambusia affinis growth and condition to assess estuarine habitat quality: A comparison of indices

Numerous indices have been used to estimate fish growth and condition however, differences in sensitivity and reliability of the methods have hampered efforts to identify appropriate indicators for routine evaluation of habitat quality in the field. We compared common morphometric (length, weight, somatic growth, length-weight condition) and biochemical (RNA:DNA ratio, relative DNA content, energy density) growth indices on the same wild-caught mosquitofish Gambusia affinis to examine their usefulness as indicators of habitat quality. A laboratory experiment was used to quantify growth rates of wild-caught G. affinis under different feeding treatments. Field studies consisted of both a short-term enclosure experiment (10 d) and weekly (7 wk) fish collections to compare growth indices in managed inflow and reference marshes during a winter/spring freshwater pulse event in upper Breton Sound, Louisiana, USA. Marshes flooded by restored freshwater pulses were capable of producing optimum growth (0.001 g DW d-1 DW = dry weight) and energetically valuable habitat (>6000 cal g-1 DW) for trophic transport. Because of differences in timing of response, morphometric and biochemical indices were generally not directly correlated, but there was clear agreement in direction and magnitude of response. The most striking difference in timing was that biochemical indices (RNA:DNA) responded more slowly to treatments than did morphometric growth indices. While gross patterns are comparable between indicators, differences in sensitivity and response time between indicators suggest that choice of indicator needs to be accounted for in interpretation and analysis of effects. ?? Inter-Research 2010, www.int-res.com.

Marine Ecology Progress Series↗

Growth rates for immature Kemp’s ridley sea turtles from a foraging area in the northern Gulf of Mexico

Examining vital rates helps clarify how environmental characteristics, biological resources and human activities affect population growth. Carapace lengths were gathered for 241 Kemp’s ridley Lepidochelys kempii sea turtles that were marked and recaptured (n = 23) between 2011 and 2019 at a foraging location in northwest Florida, USA. There was a strong correlation between length, width and weight of captured turtles. Mean ± SD size of all captured turtles was 36.6 ± 7.6 cm. Mean recapture interval was 499 ± 475.4 d. Straight-line carapace lengths at initial capture ranged from 20.6 to 53.3 cm. Growth rates from 0.21 to 12.44 cm yr -1 (mean 3.15 ± 2.64 cm) were documented and were greatest for turtles in the 20.0-29.9 cm size class. Growth rates from northwest Florida were slower than those reported from other sites in the Gulf of Mexico. These results indicate that Kemp’s ridleys recruit from oceanic habitat into coastal bays in northwest Florida, where they remain until they reach adulthood. However, some adult-sized turtles may continue to use the nearshore habitat. A gradient in growth rates in the Gulf of Mexico may occur from faster growth in the south to slower growth in the north. Fine-scale variations in resources and environmental conditions may drive regional differences in growth rates, and research on what drives these differences is needed.

Marine Ecology Progress Series↗

Increased whitebark pine (Pinus albicaulis) growth and defense under a warmer and regionally drier climate

Introduction: Tree defense characteristics play a crucial role in modulating conifer bark beetle interactions, and there is a growing body of literature investigating factors mediating tree growth and resin-based defenses in conifers. A subset of studies have looked at relationships between tree growth, resin duct morphology and climate; however, these studies are almost exclusively from lower-elevation, moisture-limited systems. The relationship between resin ducts and climate in higher-elevation, energy-limited ecosystems is currently poorly understood. Methods: In this study, we: (1) evaluated the relationship between biological trends in tree growth, resin duct anatomy, and climatic variability and (2) determined if tree growth and resin duct morphology of whitebark pine, a high-elevation conifer of management concern, is constrained by climate and/or regional drought conditions. Results: We found that high-elevation whitebark pine trees growing in an energy-limited system experienced increased growth and defense under warmer and regionally drier conditions, with climate variables explaining a substantive proportion of variation (∼20–31%) in tree diameter growth and resin duct anatomy. Discussion: Our results suggest that whitebark pine growth and defense was historically limited by short growing seasons in high-elevation environments; however, this relationship may change in the future with prolonged warming conditions.

Montana↗

Plant-derived products selectively suppress growth of the harmful alga Prymnesium parvum

Prymnesium parvum is a harmful alga found in brackish waters worldwide whose toxins can be lethal to aquatic organisms. Established field methods to control blooms of this species, however, are unavailable. Earlier studies showed that various extracts of giant reed ( Arundo donax ) can suppress P. parvum growth and that ellipticine, an allelochemical present in giant reed, is a potent algicide against this species. The unintended effects of giant reed products on nontarget organisms, however, are not fully understood. This study determined the effects of giant reed leachate (aqueous extract of dried chips) and ellipticine on growth of P. parvum and the green microalga Chlorella sorokiniana ; survival and reproduction of the planktonic crustacean Daphnia pulex ; and hatching success, larval survival, and larval swimming behavior of the teleost fish Danio rerio . Leachate made with 3 g chips L −1 was lethally toxic to P. parvum and D. pulex , stimulated C. sorokiniana growth, and impaired D. rerio behavior. Leachate at 1 g L −1 fully suppressed P. parvum growth, had moderate effects on D. pulex reproductive output, and had no effects on D. rerio . Ellipticine at 0.01 mg L −1 irreversibly inhibited P. parvum growth, acutely but reversibly inhibited C. sorokiniana growth, slightly delayed D. pulex reproduction, and had no effects on D. rerio . These observations suggest that when applied at appropriate concentrations, natural products derived from giant reed can be used as tools to specifically control P. parvum growth with minimal effects on nontarget species.

Water↗

Influence of repeated prescribed fire on tree growth and mortality in Pinus resinosa forests, northern Minnesota

Prescribed fire is widely used for ecological restoration and fuel reduction in fire-dependent ecosystems, most of which are also prone to drought. Despite the importance of drought in fire-adapted forests, little is known about cumulative effects of repeated prescribed burning on tree growth and related response to drought. Using dendrochronological data in red pine ( Pinus resinosa Ait.)-dominated forests in northern Minnesota, USA, we examined growth responses before and after understory prescribed fires between 1960 and 1970, to assess whether repeated burning influences growth responses of overstory trees and vulnerability of overstory tree growth to drought. We found no difference in tree-level growth vulnerability to drought, expressed as growth resistance, resilience, and recovery, between areas receiving prescribed fire treatments and untreated forests. Annual mortality rates during the period of active burning were also low (less than 2%) in all treatments. These findings indicate that prescribed fire can be effectively integrated into management plans and climate change adaptation strategies for red pine forest ecosystems without significant short- or long-term negative consequences for growth or mortality rates of overstory trees.

Minnesota↗