Growth rates of black caiman (Melanosuchus niger) and spectacled caiman (Caiman crocodilus) from two different Amazonian flooded habitats

2013 ◽  
Vol 34 (4) ◽  
pp. 437-449 ◽  
Author(s):  
Ronis Da Silveira ◽  
Zilca Campos ◽  
John Thorbjarnarson ◽  
William E. Magnusson

Rates of growth and survival in wild populations are affected by the physical environment, biotic interactions, and density-dependent processes, such as growth and fecundity. However, the relative importance of these factors in long-lived reptiles is poorly understood. We analyzed growth rates of Melanosuchus niger and Caiman crocodilus coexisting in two areas of the Brazilian Amazon with very different environmental characteristics. Growth rates of Caiman crocodilus at the two sites were similar, but M. niger grew more slowly in the area with higher productivity and higher density of caimans. Growth rates of the same species from other sites and of the temperate-zone Alligator mississippiensis indicate large differences among sites, but little evidence that these differences are primarily due to differences in productivity or temperature. Demographic models used to estimate sustained yields from caiman harvests should take into account the likely importance of density-dependent growth.

2002 ◽  
Vol 59 (1) ◽  
pp. 57-65 ◽  
Author(s):  
Geir Ottersen ◽  
Kristin Helle ◽  
Bjarte Bogstad

For the large Arcto-Norwegian stock of cod (Gadus morhua L.) in the Barents Sea, year-to-year variability in growth is well documented. Here three hypotheses for the observed inverse relation between abundance and the mean length-at-age of juveniles (ages 1–4) are suggested and evaluated. Based on comprehensive data, we conclude that year-to-year differences in length-at-age are mainly determined by density-independent mechanisms during the pelagic first half year of the fishes' life. Enhanced inflow from the southwest leads to an abundant cohort at the 0-group stage being distributed farther east into colder water masses, causing lower postsettlement growth rates. We can not reject density-dependent growth effects related to variability in food rations, but our data do not suggest this to be the main mechanism. Another hypothesis suggests that lower growth rates during periods of high abundance are a result of density-dependent mechanisms causing the geographic range of juveniles to extend eastwards into colder water masses. This is rejected mainly because year-to-year differences in mean length are established by age 2, which is too early for movements over large distances.


2021 ◽  
Author(s):  
◽  
Anna Clare Smith

<p>Realistic population models and effective conservation strategies require a thorough understanding of the processes that drive variation in individual growth and survival, particularly within life stages that are subject to high mortality. For fragmented marine populations it is also important to consider how processes driving variation performance may vary through space and time. In this study I assess the interaction of two primary factors driving juvenile demography: benthic habitat composition and larval history traits, in a temperate reef fish, Forsterygion lapillum (the common triplefin). It is well understood that juveniles of many marine organisms are closely associated with structured nearshore habitats as they provide resources (refuge and food sources) that are critical for juvenile growth and/or survival. Nursery habitats are often assessed using measures of fitness of juveniles inhabiting them (e.g. rates of growth). However individual fitness measures may not only be indicative of conditions experienced in the benthic phase, but also an individual's prior history. Recent evidence suggests that variation in larval traits at settlement (e.g., size and age at settlement, larval growth rate) can impact on subsequent ecological performance (e.g., feeding ability and/or predator avoidance) and therefore influence subsequent fitness (i.e. rates of growth and/or probabilities of survival). I used otolith microstructure to assess separate and joint effects of habitat composition and larval traits on the growth of young F. lapillum. Both macroalgal composition of habitat patches and larval traits affected juvenile growth rates, and results suggested that habitat composition may have the potential to mediate fitness-related advantages that may accrue to certain individuals as a result of paternal effects and/or larval dispersal history. Quantifying spatio-temporal variability in the post-settlement fitness of Individuals with that differ in larval traits is essential for effective spatial management of marine populations. I further explore the joint effects of macroalgal composition and larval traits, within the context of additional spatial and temporal environmental variation. Results provide direct evidence that habitat can mediate the strength of carryover effects, but that the impact of habitat was variable between local populations and settlement events through time. In chapter 4 of my thesis, I focus on how small-scale variation in macroalgal composition within a nursery habitat (while controlling for individual variation) can affect the strength of density dependent growth and survival rates of F. lapillum. Density-dependent survival is evident during the first 30 days after settlement, and the strength of density dependence varied as a function of macroalgal composition. Resulting variation in estimates of nursery value (i.e., the number of late-stage juveniles produced per area unit of habitat) highlight the importance of incorporating local scale variation in juvenile demography into assessments of nursery habitat. Lastly, I assess a potential strategy of fishes to persist in a wide range of benthic environments. The ability to adjust traits (i.e., phenotypic plasticity) may allow organisms that encounter a range of unpredictable environmental conditions to maximise fitness within a single generation. In chapter 5 I explore patterns of variation in morphology of juvenile F. lapillum from two different subpopulations and from different macroalgal habitats. I evaluate possible evidence for constraints on morphological variation arising from variation in growth rate prior to and following settlement. Results suggest that for organisms with complex life cycles, variation in growth rates experienced during dispersal may constrain plasticity in later stages.</p>


2021 ◽  
Author(s):  
◽  
Anna Clare Smith

<p>Realistic population models and effective conservation strategies require a thorough understanding of the processes that drive variation in individual growth and survival, particularly within life stages that are subject to high mortality. For fragmented marine populations it is also important to consider how processes driving variation performance may vary through space and time. In this study I assess the interaction of two primary factors driving juvenile demography: benthic habitat composition and larval history traits, in a temperate reef fish, Forsterygion lapillum (the common triplefin). It is well understood that juveniles of many marine organisms are closely associated with structured nearshore habitats as they provide resources (refuge and food sources) that are critical for juvenile growth and/or survival. Nursery habitats are often assessed using measures of fitness of juveniles inhabiting them (e.g. rates of growth). However individual fitness measures may not only be indicative of conditions experienced in the benthic phase, but also an individual's prior history. Recent evidence suggests that variation in larval traits at settlement (e.g., size and age at settlement, larval growth rate) can impact on subsequent ecological performance (e.g., feeding ability and/or predator avoidance) and therefore influence subsequent fitness (i.e. rates of growth and/or probabilities of survival). I used otolith microstructure to assess separate and joint effects of habitat composition and larval traits on the growth of young F. lapillum. Both macroalgal composition of habitat patches and larval traits affected juvenile growth rates, and results suggested that habitat composition may have the potential to mediate fitness-related advantages that may accrue to certain individuals as a result of paternal effects and/or larval dispersal history. Quantifying spatio-temporal variability in the post-settlement fitness of Individuals with that differ in larval traits is essential for effective spatial management of marine populations. I further explore the joint effects of macroalgal composition and larval traits, within the context of additional spatial and temporal environmental variation. Results provide direct evidence that habitat can mediate the strength of carryover effects, but that the impact of habitat was variable between local populations and settlement events through time. In chapter 4 of my thesis, I focus on how small-scale variation in macroalgal composition within a nursery habitat (while controlling for individual variation) can affect the strength of density dependent growth and survival rates of F. lapillum. Density-dependent survival is evident during the first 30 days after settlement, and the strength of density dependence varied as a function of macroalgal composition. Resulting variation in estimates of nursery value (i.e., the number of late-stage juveniles produced per area unit of habitat) highlight the importance of incorporating local scale variation in juvenile demography into assessments of nursery habitat. Lastly, I assess a potential strategy of fishes to persist in a wide range of benthic environments. The ability to adjust traits (i.e., phenotypic plasticity) may allow organisms that encounter a range of unpredictable environmental conditions to maximise fitness within a single generation. In chapter 5 I explore patterns of variation in morphology of juvenile F. lapillum from two different subpopulations and from different macroalgal habitats. I evaluate possible evidence for constraints on morphological variation arising from variation in growth rate prior to and following settlement. Results suggest that for organisms with complex life cycles, variation in growth rates experienced during dispersal may constrain plasticity in later stages.</p>


2004 ◽  
Vol 61 (9) ◽  
pp. 1616-1626 ◽  
Author(s):  
Michael A Etnier

Analysis of length-at-age measurements of archived skeletal material shows that somatic growth rates of male northern fur seals (Callorhinus ursinus) vary inversely with population density. Von Bertalanffy growth curves were estimated for two series of known-age mandibles collected 1911–1920 (n = 156) and 1940–1953 (n = 151), time periods representing the historic population minimum and maximum, respectively. Mandibles from the former time period are larger than mandibles from the latter time period, suggesting a density-dependent response in somatic growth. Although density-dependent growth in northern fur seals has been suggested before, previous studies have been hampered by the potentially confounding factors of fisheries interactions, variable environmental conditions, and harvest of adult female northern fur seals. The material analyzed here pre-dates the substantial development of the Bering Sea groundfish fishery and the period of heaviest culling of females. Likewise, the two time periods examined are characterized by broadly similar climatic and environmental conditions. Therefore, the results support the hypothesis that measurements of somatic growth rates provide an index of population levels relative to carrying capacity. Growth rate studies could therefore be used to evaluate the current population status of northern fur seals.


Author(s):  
K. Thomas Jensen

To examine density-dependent effects on growth in Cerastoderma edule (L.) (Bivalvia), growth rates of individual cockles established by chance at high and low densities on the same intertidal mudflat in two different years (1984 and 1989) were compared. Two-year-old cockles occurring at high densities (>2000 individuals m-2 in 1984) attained mean lengths from 16.1 to 18.8 mm on the lower shore at the end of their third growing season, while low-density cockles (<50 individuals m-2 in 1989) of the same age reached mean lengths in the range of26.5 to 30.3mm. In terms of individual weight the difference between cockles from the two periods was even more striking, as the flesh ash-free dry-weight of a cockle from 1984 constituted only 7% of that from a 1989 cockle. During both periods growth in cockles increased with the duration of tidal submersion, but the interannual growth differences exceeded by far the effect of differences in submersion time.


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