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At least 19 recordsLinked to original sources

Evidence for growth hormone/insulin-like growth factor I axis regulation of seawater acclimation in the euryhaline teleost Fundulus heteroclitus

The ability of ovine growth hormone (oGH), recombinant bovine insulin-like growth factor I (rbIGF-I), recombinant human insulin-like growth factor II (rhIGF-II), and bovine insulin to increase hypoosmoregulatory capacity in the euryhaline teleost Fundulus heteroclitus was examined. Fish acclimated to brackish water (BW, 10 ppt salinity, 320 mOsm/kg H 2 O) were injected with a single dose of hormone and transferred to seawater (SW, 35 ppt salinity, 1120 mOsm/kg H 2 O) 2 days later. Fish were sampled 24 h after transfer and plasma osmolality, plasma glucose, and gill Na + ,K + -ATPase activity were examined. Transfer from BW to SW increased plasma osmolality and gill Na + ,K + -ATPase activity. Transfer from BW to BW had no effect on these parameters. rbIGF-I (0.05, 0.1, and 0.2 μg/g) improved the ability to maintain plasma osmolality and to increase gill Na + , K + -ATPase activity in a dose-dependent manner. oGH (0.5, 1, and 2 μg/g) also increased hypoosmoregulatory ability but only the higher doses (2 μg/g) significantly increased gill Na + ,K + -ATPase activity. oGH (1 μg/g) and rbIGF-I (0.1 μg/g) had a significantly greater effect on plasma osmolality and gill Na + ,K + -ATPase activity than either hormone alone. rhIGF-II (0.05, 0.1, and 0.2 μg/g) and bovine insulin (0.01 and 0.05 μg/g) were without effect. The results suggest a role of GH and insulin-like growth factor I (IGF-I) in seawater acclimation of F. heteroclitus. Based on these findings and previous studies, it is concluded that the capacity of the GH/IGF-I axis to increase hypoosmoregulatory ability may be a common feature of euryhalinity in teleosts.

Connecticut↗

Variations in growth of roseate tern (Sterna dougallii) chicks: II. Early growth as an index of parental quality

We measured growth of Roseate Tern (Sterna dougallii) chicks at a colony in Connecticut in 10 successive years. Data on body mass during the first three to four days of life were fitted to a quadratic regression model, yielding three parameters of early growth for each of 1,551 chicks: mass at hatching (Mo), linear growth (a) and quadratic growth (b). First chicks in each brood (A-chicks) exceeded second chicks (B-chicks) in each of the three growth parameters; A-chicks from broods of two grew faster than single chicks during the first three days. Mo depended on egg mass, hatch order, hatch date, and year. The linear coefficient (a) depended on hatch date, hatch order, and year, but not on egg mass or Mo. The quadratic coefficient (b) depended on a, hatch date, Mo, and hatch order. Subsequent growth and survival of chicks were predicted well by these parameters of early growth, with b contributing more to these predictions than Mo or a. After controlling for effects of early growth, none of the other variables measured (hatch date, egg mass, parental age, hatch interval between chicks, mass difference between chicks, female-female pairing, or trapping) contributed significantly to explaining later growth and survival. Year effects were substantial in only two of the 10 years of study. Individual pairs were consistent in performance (as indexed by chick growth) in successive years. These results suggest that growth and survival of Roseate Tern chicks are determined primarily by parental quality; much of the information about parental quality is expressed by the time the eggs are laid, and most of it is expressed by the time the chicks are three days old.

Condor↗

Density, ages, and growth rates in old-growth and young-growth forests in coastal Oregon

We studied the ages and diameter growth rates of trees in former Douglas-fir (Pseudotsuga menziesii (Mirb.)Franco) old-growth stands on 10 sites and compared them with young-growth stands (50-70 years old, regenerated after timber harvest) in the Coast Range of western Oregon. The diameters and diameter growth rates for the first 100 years of trees in the old-growth stands were significantly greater than those in the young-growth stands. Growth rates in the old stands were comparable with those from long-term studies of young stands in which density is about 100-120 trees/ha; often young-growth stand density is well over 500 trees/ha. Ages of large trees in the old stands ranged from 100 to 420 years; ages in young stands varied by only about 5 to 10 years. Apparently, regeneration of old-growth stands on these sites occurred over a prolonged period, and trees grew at low density with little self-thinning; in contrast, after timber harvest, young stands may develop with high density of trees with similar ages and considerable self-thinning. The results suggest that thinning may be needed in dense young stands where the management objective is to speed development of old-growth characteristics.

Canadian Journal of Forest Research↗

Repeated acute stress reduces growth rate of Atlantic salmon parr and alters plasma levels of growth hormone, insulin-like growth factor I and cortisol

Atlantic salmon ( Salmo salar ) parr were subjected to acute handling stresses and growth-monitored for at least 30 days. In fish stressed twice daily, growth rate in weight was 61% lower than controls after 11 days (1.00 vs. 2.57% day −1 ) and over a 30 day period it was 50% lower than controls (1.53 vs. 3.07% day −1 ). In fish stressed once daily, growth rate was 18% lower than controls after 10 days (2.17 vs. 2.63% day −1 ) and over a 30-day period it was 34% lower than controls (1.71 vs. 2.59% day −1 ). In fish stressed once daily, food consumption was reduced by 62% and 37% after 17 and 37 days, respectively. At the end of 40 days of acute stress once daily, control and stressed fish were sampled 1 h prior to, 3 and 7 h after a stress event. Plasma growth hormone levels were significantly higher in the stressed group than in the controls prior to and 7 h after stress. Plasma insulin-like growth factor I (IGF-I) levels were higher in the stressed group only 3 and 7 h after stress. Plasma cortisol levels were lower in the stressed group prior to and 3 h after stress. The results indicate that acute stressors decrease growth of Atlantic salmon parr, with increasing frequency of stress having a more rapid and greater effect.

Aquaculture↗

Seasonal variations in ectotherm growth rates: Quantifying growth as an intermittent non steady state compensatory process

Generally, growth rates of living organisms are considered to be at steady state, varying only under environmental forcing factors. For example, these rates may be described as a function of light for plants or organic food resources for animals and these could be regulated (or not) by temperature or other conditions. But, what are the consequences for an individual's growth (and also for the population growth) if growth rate variations are themselves dynamic and not steady state? For organisms presenting phases of dormancy or long periods of stress, this is a crucial question. A dynamic perspective for quantifying short-term growth was explored using the daily growth record of the scallop Pecten maximus (L.). This species is a good biological model for ectotherm growth because the shell records growth striae daily. Independently, a generic mathematical function representing the dynamics of mean daily growth rate (MDGR) was implemented to simulate a diverse set of growth patterns. Once the function was calibrated with the striae patterns, the growth rate dynamics appeared as a forced damped oscillation during the growth period having a basic periodicity during two transitory phases (mean duration 43. days) and appearing at both growth start and growth end. This phase is most likely due to the internal dynamics of energy transfer within the organism rather than to external forcing factors. After growth restart, the transitory regime represents successive phases of over-growth and regulation. This pattern corresponds to a typical representation of compensatory growth, which from an evolutionary perspective can be interpreted as an adaptive strategy to coping with a fluctuating environment.

Journal of Sea Research↗

Structure and development of old-growth, unmanaged second-growth, and extended rotation Pinus resinosa forests in Minnesota, USA

The structure and developmental dynamics of old-growth forests often serve as important baselines for restoration prescriptions aimed at promoting more complex structural conditions in managed forest landscapes. Nonetheless, long-term information on natural patterns of development is rare for many commercially important and ecologically widespread forest types. Moreover, the effectiveness of approaches recommended for restoring old-growth structural conditions to managed forests, such as the application of extended rotation forestry, has been little studied. This study uses several long-term datasets from old growth, extended rotation, and unmanaged second growth Pinus resinosa (red pine) forests in northern Minnesota, USA, to quantify the range of variation in structural conditions for this forest type and to evaluate the effectiveness of extended rotation forestry at promoting the development of late-successional structural conditions. Long-term tree population data from permanent plots for one of the old-growth stands and the extended rotation stands (87 and 61 years, respectively) also allowed for an examination of the long-term structural dynamics of these systems. Old-growth forests were more structurally complex than unmanaged second-growth and extended rotation red pine stands, due in large part to the significantly higher volumes of coarse woody debris (70.7 vs. 11.5 and 4.7 m 3 /ha, respectively) and higher snag basal area (6.9 vs. 2.9 and 0.5 m 2 /ha, respectively). In addition, old-growth forests, although red pine-dominated, contained a greater abundance of other species, including Pinus strobus , Abies balsamea , and Picea glauca relative to the other stand types examined. These differences between stand types largely reflect historic gap-scale disturbances within the old-growth systems and their corresponding structural and compositional legacies. Nonetheless, extended rotation thinning treatments, by accelerating advancement to larger tree diameter classes, generated diameter distributions more closely approximating those found in old growth within a shorter time frame than depicted in long-term examinations of old-growth structural development. These results suggest that extended rotation treatments may accelerate the development of old-growth structural characteristics, provided that coarse woody debris and snags are deliberately retained and created on site. These and other developmental characteristics of old-growth systems can inform forest management when objectives include the restoration of structural conditions found in late-successional forests.

Minnesota↗

Latitudinal comparisons of walleye growth in North America and factors influencing growth of walleyes in Kansas reservoirs

We compared the growth of walleyes Stizostedion vitreum in Kansas to that of other populations throughout North America and determined the effects of the abundance of gizzard shad Dorosoma cepedianum and temperature on the growth of walleyes in Kansas reservoirs. Age was estimated from scales and otoliths collected from walleyes (N = 2,072) sampled with gill nets from eight Kansas reservoirs during fall in 1991-1999. Age-0 gizzard shad abundance was indexed based on summer seining information, and temperature data were obtained from the National Oceanic and Atmospheric Administration. Parameter estimates of von Bertalanffy growth models indicated that the growth of walleyes in Kansas was more similar to that of southern latitude populations (e.g., Mississippi and Texas) than to that of northern (e.g., Manitoba, Minnesota and South Dakota) or middle latitude (e.g., Colorado and Iowa) populations. Northern and middle latitude populations had lower mean back-calculated lengths at age 1, lower growth coefficients, and greater longevity than southern and Kansas populations. A relative growth index (RGI; [Lt/Ls ] ?? 100, where Lt is the observed length at age and Ls is the age-specific standard length derived from a pooled von Bertalanffy growth model) and standardized percentile values (percentile values of mean back-calculated lengths at age) indicated that the growth of walleyes in Kansas was above average compared with that of other populations in North America. The annual growth increments of Kansas walleyes were more variable among years than among reservoirs. The growth increments of age-0 and age-1 walleyes were positively related to the catch rates of gizzard shad smaller than 80 mm, whereas the growth of age-2 and age-3 walleyes was inversely related to mean summer air temperature. Our results provide a framework for comparing North American walleye populations, and our proposed RGI provides a simple, easily interpreted index of growth.

North American Journal of Fisheries Management↗

Stimulation of coho salmon growth by insulin-like growth factor I

The effect of insulin-like growth factor I on growth rate of coho salmon ( Oncorhynchus kisutch ) was examined. Juvenile coho salmon received implants of osmotic minipumps containing recombinant bovine insulin-like growth factor I (rbIGF-I) or saline for a period of 3 to 4 weeks. High doses of rbIGF-I (>0.13 μg · g −1 · d −1 ) resulted in hypoglycemia and death. In 2-year-old coho salmon, 0.09 μg · g −1 · d −1 rbIGF-I administered for 25 days doubled linear growth rate and increased growth rate in weight by 40%. In rapidly growing, 1-year-old coho salmon, growth rate was not altered by rbIGF-I at 0.01 or 0.05 μg · g −1 · d −1 for 31 days. In ration-limited fish exhibiting slow growth in the control group, rbIGF-I (0.02 to 0.12 μg · g −1 · d −1 ) increased linear growth rate by up to threefold and growth rate in weight by up to fourfold. The results indicate that exogenous treatment with mammalian IGF-I can stimulate coho salmon growth under some conditions, and that endogenous IGF-I may be an important factor in regulating growth of teleosts.

General and Comparative Endocrinology↗

Tree growth and competition in an old-growth Picea abies forest of boreal Sweden: influence of tree spatial patterning

Question: What factors best characterize tree competitive environments in this structurally diverse old-growth forest, and do these factors vary spatially within and among stands? Location: Old-growth Picea abies forest of boreal Sweden. Methods: Using long-term, mapped permanent plot data augmented with dendrochronological analyses, we evaluated the effect of neighbourhood competition on focal tree growth by means of standard competition indices, each modified to include various metrics of trees size, neighbour mortality weighting (for neighbours that died during the inventory period), and within-neighbourhood tree clustering. Candidate models were evaluated using mixed-model linear regression analyses, with mean basal area increment as the response variable. We then analysed stand-level spatial patterns of competition indices and growth rates (via kriging) to determine if the relationship between these patterns could further elucidate factors influencing tree growth. Results: Inter-tree competition clearly affected growth rates, with crown volume being the size metric most strongly influencing the neighbourhood competitive environment. Including neighbour tree mortality weightings in models only slightly improved descriptions of competitive interactions. Although the within-neighbourhood clustering index did not improve model predictions, competition intensity was influenced by the underlying stand-level tree spatial arrangement: stand-level clustering locally intensified competition and reduced tree growth, whereas in the absence of such clustering, inter-tree competition played a lesser role in constraining tree growth. Conclusions: Our findings demonstrate that competition continues to influence forest processes and structures in an old-growth system that has not experienced major disturbances for at least two centuries. The finding that the underlying tree spatial pattern influenced the competitive environment suggests caution in interpreting traditional tree competition studies, in which tree spatial patterning is typically not taken into account. Our findings highlight the importance of forest structure – particularly the spatial arrangement of trees – in regulating inter-tree competition and growth in structurally diverse forests, and they provide insight into the causes and consequences of heterogeneity in this old-growth system.

V�sterbotten County↗

Using a laboratory-based growth model to estimate mass- and temperature-dependent growth parameters across populations of juvenile Chinook Salmon

To estimate the parameters that govern mass- and temperature-dependent growth, we conducted a meta-analysis of existing growth data from juvenile Chinook Salmon Oncorhynchus tshawytscha that were fed an ad libitum ration of a pelleted diet. Although the growth of juvenile Chinook Salmon has been well studied, research has focused on a single population, a narrow range of fish sizes, or a narrow range of temperatures. Therefore, we incorporated the Ratkowsky model for temperature-dependent growth into an allometric growth model; this model was then fitted to growth data from 11 data sources representing nine populations of juvenile Chinook Salmon. The model fit the growth data well, explaining 98% of the variation in final mass. The estimated allometric mass exponent (b) was 0.338 (SE = 0.025), similar to estimates reported for other salmonids. This estimate of b will be particularly useful for estimating mass-standardized growth rates of juvenile Chinook Salmon. In addition, the lower thermal limit, optimal temperature, and upper thermal limit for growth were estimated to be 1.8°C (SE = 0.63°C), 19.0°C (SE = 0.27°C), and 24.9°C (SE = 0.02°C), respectively. By taking a meta-analytical approach, we were able to provide a growth model that is applicable across populations of juvenile Chinook Salmon receiving an ad libitum ration of a pelleted diet.

Transactions of the American Fisheries Society↗

Growth performance of Rainbow Trout in reservoir tributaries and implications for steelhead growth potential above Skagit River dams

Objective In the Pacific Northwest (USA), Pacific salmon Oncorhynchus spp. populations have been declining significantly for decades, prompting stakeholders to respond with a variety of conservation and restoration measures. One such measure being considered in the Skagit River basin (Washington, USA) is the introduction of steelhead Oncorhynchus mykiss (anadromous Rainbow Trout) above the impassable Gorge, Diablo, and Ross dams to bolster their populations. Because freshwater growth is key to survival at subsequent life stages, we evaluated current trends in size and growth of Rainbow Trout among key tributaries to Gorge, Diablo, and Ross reservoirs using empirical data collection and bioenergetics modeling. Methods For nine candidate streams, a bioenergetics model was used to assess how temperature and prey consumption affected growth performance of Rainbow Trout between annuli 1 and 2, and 2 and 3. Thermal scenarios were created to evaluate how fish growth responded to temperature variability while total annual consumption was constrained within empirical growth estimates. We then compared these results to back-calculated size thresholds established by size-at-age observed in wild steelhead adults that returned to the Skagit River below the dams. Result Of the streams proposed for introductions, there was one instance (McMillan Creek) in the nominal simulations where growth met or exceeded the size at annulus 2 or 3 of a returning adult steelhead (24.9 g at annulus 2 and 50.3 g at annulus 3). Modeled growth under different thermal scenarios showed that colder temperatures (0.1–10.7°C, Canyon Creek) produced higher growth than under the nominal or warm scenarios (2.0–15.3°C, Canyon Creek), as well as one additional tributary where size at annulus 2 or 3 (±2 SE) was comparable to the threshold established by adult steelhead below the dams (Big Beaver Creek, annulus 3). Conclusion These results suggest Rainbow Trout growth is most limited by prey availability in the examined upper Skagit tributaries.

Washington↗

Linking ecosystem processes to consumer growth rates: Gross primary productivity as a driver of freshwater fish somatic growth in a resource-limited river

Individual growth can exert strong controls on population dynamics and be constrained by resource acquisition rates. Difficulty in accurately quantifying resource availability over large spatial extents and at high temporal frequency often limits attempts to understand the extent that resources limit individual growth. Daily estimates of stream metabolism, including gross primary productivity (GPP), are increasingly available but have not, to our knowledge, been linked to fish growth. Here we examine how GPP, water temperature, high flow and turbidity are linked to spatiotemporal variation in growth of flannelmouth sucker (Catostomus latipinnis). We fit state space growth models to six years of mark-recapture data collected in four river reaches spanning 300 river kilometers. Consistent with past research in this system, we find that water temperature is the dominant driver of spatiotemporal variation in growth. However, we also find that GPP is strongly linked to fish growth. Fish growth is likely to be linked to stream metabolism in other systems where overall productivity, not the quality of primary producers, limits the food webs that support fish growth.

Arizona↗

The effect of size and competition on tree growth rate in old-growth coniferous forests

Tree growth and competition play central roles in forest dynamics. Yet models of competition often neglect important variation in species-specific responses. Furthermore, functions used to model changes in growth rate with size do not always allow for potential complexity. Using a large data set from old-growth forests in California, models were parameterized relating growth rate to tree size and competition for four common species. Several functions relating growth rate to size were tested. Competition models included parameters for tree size, competitor size, and competitor distance. Competitive strength was allowed to vary by species. The best ranked models (using Akaike’s information criterion) explained between 18% and 40% of the variance in growth rate, with each species showing a strong response to competition. Models indicated that relationships between competition and growth varied substantially among species. The results also suggested that the relationship between growth rate and tree size can be complex and that how we model it can affect not only our ability to detect that complexity but also whether we obtain misleading results. In this case, for three of four species, the best model captured an apparent and unexpected decline in potential growth rate for the smallest trees in the data set.

Canadian Journal of Forest Research↗

Long-term increases in young-of-the-year growth of Arctic cisco Coregonus autumnalis and environmental influences

Arctic cisco Coregonus autumnalis young-of-year (YOY) growth was used as a proxy to examine the long-term response of a high-latitude fish population to changing climate from 1978 to 2004. YOY growth increased over time (r2 = 0·29) and was correlated with monthly averages of the Arctic oscillation index, air temperature, east wind speed, sea-ice concentration and river discharge with and without time lags. Overall, the most prevalent correlates to YOY growth were sea-ice concentration lagged 1 year (significant correlations in 7 months; r 2 = 0·14-0·31) and Mackenzie River discharge lagged 2 years (significant correlations in 8 months; r 2 = 0·13-0·50). The results suggest that decreased sea-ice concentrations and increased river discharge fuel primary production and that life cycles of prey species linking increased primary production to fish growth are responsible for the time lag. Oceanographic studies also suggest that sea ice concentration and fluvial inputs from the Mackenzie River are key factors influencing productivity in the Beaufort Sea. Future research should assess the possible mechanism relating sea ice concentration and river discharge to productivity at upper trophic levels.

Journal of Fish Biology↗

Growth of coast redwood and Douglas-fir following thinning in second-growth forests at Redwood National Park and Headwaters Forest Reserve

Managers of second-growth forests at Redwood National Park and the Bureau of Land Management’s Headwaters Forest Reserve encourage the development of late seral forest characteristics using mechanical thinning, where competing vegetation is removed to promote growth of residual trees. Yet the ability to quantify and reliably predict outcomes of treatments such as these is hindered by the long time scales at which forests respond to thinning. Here we present analyses of tree growth at Redwood National Park (RNP) and Headwaters Forest Reserve (HDWT) from sites that have had > 5 years to respond to thinning treatments. Compared to untreated stands, thinned stands had lower stem density (trees ha -1 ) and basal area (m 2 ha -1 ), primarily due to removal of Douglas-fir ( Pseudotsuga menziesii (Mirb.) Franco). Individual tree growth (basal area increment, BAI, m 2 yr -1 ) was related to tree size (basal area, m 2 ) and treatment history, with the highest growth rates observed in large trees. Both redwood ( Sequoia sempervirens (D. Don) Endl.) and Douglas-fir appeared to have a small, but detectable, positive growth response to thinning treatments. Early results suggest a large degree of variation among sites, with possible systematic differences in growth responses between RNP and HDWT. Future work will focus on identifying site-level differences (site quality, local competition, slope, aspect, stand age, distance from the ocean) to improve our understanding of the growth response.

Redwood National Park and Headwaters Forest Reserv↗

Long-term patterns of diameter and basal area growth of old-growth Douglas-fir trees in western Oregon

Diameter growth and age data collected from stumps of 505 recently cut old-growth Douglas-fir (Pseudotsuga menziesii (Mirb.) Franco) trees at 28 sample locations in western Oregon (U.S.A.) indicated that rapid early and sustained growth of old Douglas-fir trees were extremely important in terms of attaining large diameters at ages 100a??300 years. The diameters of the trees at ages 100a??300 years (D100a??D300) were strongly, positively, and linearly related to their diameters and basal area growth rates at age 50 years. Average periodic basal area increments (PAIBA) of all trees increased for the first 30a??40 years and then plateaued, remaining relatively high and constant from age 50 to 300 years. Average PAIBA of the largest trees at ages 100a??300 years were significantly greater by age 20 years than were those of smaller trees at ages 100a??300 years. The site factors province, site class, slope, aspect, elevation, and establishment year accounted for little of the variation observed in basal area growth at age 50 years and D100a??D300. The mean age range for old-growth Douglas-fir at the sample locations was wide (174 years). The hypothesis that large-diameter old-growth Douglas-fir developed at low stand densities was supported by these observations.

Canadian Journal of Forest Research↗

Recent growth of conifer species of western North America: Assessing spatial patterns of radial growth trends

We explored spatial patterns of low-frequency variability in radial tree growth among western North American conifer species and identified predictors of the variability in these patterns. Using 185 sites from the International Tree-Ring Data Bank, each of which contained 10a??60 raw ring-width series, we rebuilt two chronologies for each site, using two conservative methods designed to retain any low-frequency variability associated with recent environmental change. We used factor analysis to identify regional low-frequency patterns in site chronologies and estimated the slope of the growth trend since 1850 at each site from a combination of linear regression and time-series techniques. This slope was the response variable in a regression-tree model to predict the effects of environmental gradients and species-level differences on growth trends. Growth patterns at 27 sites from the American Southwest were consistent with quasi-periodic patterns of drought. Either 12 or 32 of the 185 sites demonstrated patterns of increasing growth between 1850 and 1980 A.D., depending on the standardization technique used. Pronounced growth increases were associated with high-elevation sites (above 3000 m) and high-latitude sites in maritime climates. Future research focused on these high-elevation and high-latitude sites should address the precise mechanisms responsible for increased 20th century growth.

Canadian Journal of Forest Research↗

Allowing macroalgae growth forms to emerge: Use of an agent-based model to understand the growth and spread of macroalgae in Florida coral reefs, with emphasis on Halimeda tuna

The growth patterns of macroalgae in three-dimensional space can provide important information regarding the environments in which they live, and insights into changes that may occur when those environments change due to anthropogenic and/or natural causes. To decipher these patterns and their attendant mechanisms and influencing factors, a spatially explicit model has been developed. The model SPREAD (SPatially-explicit Reef Algae Dynamics), which incorporates the key morphogenetic characteristics of clonality and morphological plasticity, is used to investigate the influences of light, temperature, nutrients and disturbance on the growth and spatial occupancy of dominant macroalgae in the Florida Reef Tract. The model species, Halimeda and Dictyota spp., are modular organisms, with an 'individual' being made up of repeating structures. These species can also propagate asexually through clonal fragmentation. These traits lead to potentially indefinite growth and plastic morphology that can respond to environmental conditions in various ways. The growth of an individual is modeled as the iteration of discrete macroalgal modules whose dynamics are affected by the light, temperature, and nutrient regimes. Fragmentation is included as a source of asexual reproduction and/or mortality. Model outputs are the same metrics that are obtained in the field, thus allowing for easy comparison. The performance of SPREAD was tested through sensitivity analysis and comparison with independent field data from four study sites in the Florida Reef Tract. Halimeda tuna was selected for initial model comparisons because the relatively untangled growth form permits detailed characterization in the field. Differences in the growth patterns of H. tuna were observed among these reefs. SPREAD was able to closely reproduce these variations, and indicate the potential importance of light and nutrient variations in producing these patterns. ?? 2008 Elsevier B.V.

Ecological Modelling↗