scholarly journals Diet and divergence of introduced smallmouth bass (Micropterus dolomieu) populations

2005 ◽  
Vol 62 (8) ◽  
pp. 1720-1732 ◽  
Author(s):  
Erin S Dunlop ◽  
Judi A Orendorff ◽  
Brian J Shuter ◽  
F Helen Rodd ◽  
Mark S Ridgway

We examine the degree and causes of divergence in growth and reproduction in two populations of smallmouth bass (Micropterus dolomieu) introduced a century ago. Despite a common source, the Provoking Lake population now has a higher population density and slower growing individuals than the Opeongo Lake population. Using this system, we test the predictions of life history theory that delayed maturation and reduced reproductive investment are expected in high density populations with slow individual growth rates. Observations on both populations run directly counter to the aforementioned expectations. Instead, Provoking males have smaller sizes and younger ages at nesting and higher gonad masses than Opeongo males; Provoking females have smaller sizes at maturity, larger egg sizes, and higher ovarian dry masses than Opeongo females. Temperature, food availability, diet ontogeny, young-of-the-year mortality, and adult mortality were examined as plausible contributors to the divergence. Results suggest that low food availability, likely caused or mediated by intraspecific competition for prey, and lack of large prey in the diet are contributing to the slow growth, increased reproductive investment, and higher mortality following reproduction in Provoking. This study provides insight into the processes that produce rapid divergence of life history in a species exhibiting parental care.

2019 ◽  
Vol 66 (4) ◽  
pp. 373-382 ◽  
Author(s):  
Mar Comas ◽  
Senda Reguera ◽  
Francisco J Zamora-Camacho ◽  
Gregorio Moreno-Rueda

Abstract Lifespan is one of the main components of life history. Shorter lifespans can be expected in marginal habitats. However, in the case of ectotherms, lifespan typically increases with altitude, even though temperature—one of the main factors to determine ectotherms’ life history—declines with elevation. This pattern can be explained by the fact that a shorter activity time favors survival. In this study, we analyzed how lifespan and other life-history traits of the lizard Psammodromus algirus vary along a 2,200 m elevational gradient in Sierra Nevada (SE Spain). Populations at intermediate altitudes (1,200–1,700 m), corresponding to the optimal habitat for this species, had the shortest lifespans, whereas populations inhabiting marginal habitats (at both low and at high altitudes) lived longest. Therefore, this lizard did not follow the typical pattern of ectotherms, as it also lived longer at the lower limit of its distribution, nor did it show a longer lifespan in areas with optimal habitats. These results might be explained by a complex combination of different gradients along the mountain, namely that activity time decreases with altitude whereas food availability increases. This could explain why lifespan was maximum at both high (limited activity time) and low (limited food availability) altitudes, resulting in similar lifespans in areas with contrasting environmental conditions. Our findings also indicated that reproductive investment and body condition increase with elevation, suggesting that alpine populations are locally adapted.


Web Ecology ◽  
2000 ◽  
Vol 1 (1) ◽  
pp. 1-10 ◽  
Author(s):  
K. I. Stergiou

Abstract. The available quantitative information (age, growth, maturation and mortality) for 103 fish stocks in Hellenic Seas was analysed here in the context of life-history theory and compared with similar information from other areas of the world. The results showed that the fish species and stocks inhabiting Hellenic waters are generally small in size, have low longevity, mature at an early age and size, and probably suffer high adult mortality rates. Such a pattern most probably is an adaptation to the synergetic combination of highly oligotrophic conditions and high subtropical temperatures prevailing in Hellenic waters and is consistent with life-history theory. Finally, the auximetric grid was used to compare the growth of four species, each represented by more than six stocks. The results revealed that the growth spaces occupied by the four species reflect their strikingly different feeding habits, especially with respect to the size of prey and the relative importance of fish prey to their diet.


2021 ◽  
pp. 1-11
Author(s):  
Gerlinde Höbel ◽  
Robb Kolodziej ◽  
Dustin Nelson ◽  
Christopher White

Abstract Information on how organisms allocate resources to reproduction is critical for understanding population dynamics. We collected clutch size (fecundity) and egg size data of female Eastern Gray Treefrogs, Hyla versicolor, and examined whether observed patterns of resource allocation are best explained by expectations arising from life history theory or by expected survival and growth benefits of breeding earlier. Female Hyla versicolor showed high between-individual variation in clutch and egg size. We did not observe maternal allocation trade-offs (size vs number; growth vs reproduction) predicted from life history theory, which we attribute to the large between-female variation in resource availability, and the low survival and post-maturity growth rate observed in the study population. Rather, clutches are larger at the beginning of the breeding season, and this variation in reproductive investment aligns with seasonal variation in ecological factors affecting offspring growth and survival.


2005 ◽  
Vol 62 (4) ◽  
pp. 844-853 ◽  
Author(s):  
Erin S Dunlop ◽  
Brian J Shuter ◽  
Mark S Ridgway

In this study, we examine the divergence in growth and maturation between two populations of smallmouth bass (Micropterus dolomieu) introduced from a common source a century ago. To determine if the divergence in maturation is simply a plastic response to differences in growth rate, we use a new approach to estimate and then compare the probabilistic maturation reaction norms (PMRNs) for each population. The PMRNs for 5-year-old males are similar in the two populations, suggesting that the observed divergence in maturation is largely a plastic response to growth rate differences. For one population, we document the time course of maturation changes for the 60-year period from 1937 through 1990; while the mean length at maturation for 5-year-old males exhibits a steady downward trend (beginning at 31 cm and ending at 26 cm), their PMRNs vary over a much narrower range (25–27 cm) and do not exhibit a consistent temporal trend. These observations are consistent with the hypothesis that most of the observed change in maturation since introduction is a product of phenotypic plasticity, driven by environmentally based differences in growth rate. Our study provides an instructive example of how the PMRN approach can be used to isolate the role of growth rate variation in generating life history differences.


2005 ◽  
Vol 62 (4) ◽  
pp. 791-801 ◽  
Author(s):  
David N Reznick ◽  
Cameron K Ghalambor

Life history theory predicts that high adult mortality rates select for earlier maturity and increased reproduction. If such evolution occurs in response to the commercial exploitation of natural fish populations, then the correlated reduction in body size would reduce the yield of the fishery. Earlier maturity and reduced body size are seen in commercially exploited populations. Here, we compare the life histories of natural populations of guppies (Poecilia reticulata) from Trinidad that live in either high- or low-predation environments, which serve as surrogates for the presence or absence of commercial fishing. We can quantify mortality rate and life history variables, including age and size at maturity, in the laboratory and in nature. We have manipulated mortality rates in nature and measured the rate of evolution. High mortality selects for earlier maturity at a smaller size, as observed in commercial fisheries and as predicted by theory. Furthermore, the nature and magnitude of predator-induced mortality are comparable to those caused by commercial fishing. The rate of evolution in guppies predicts similar evolution in commercial fisheries on a time scale of decades. These attributes support arguments that humans, like predators, have acted as an agent of selection when exploiting populations of fish.


2009 ◽  
Vol 5 (6) ◽  
pp. 802-804 ◽  
Author(s):  
Ben L. Phillips

Individuals in the vanguard of a species invasion face altered selective conditions when compared with conspecifics behind the invasion front. Assortment by dispersal ability on the expanding front, for example, drives the evolution of increased dispersal, which, in turn, leads to accelerated rates of invasion. Here I propose an additional evolutionary mechanism to explain accelerating invasions: shifts in population growth rate ( r ). Because individuals in the vanguard face lower population density than those in established populations, they should (relative to individuals in established populations) experience greater r -selection. To test this possibility, I used the ongoing invasion of cane toads ( Bufo marinus ) across northern Australia. Life-history theory shows that the most efficient way to increase the rate of population growth is to reproduce earlier. Thus, I predict that toads on the invasion front will exhibit faster individual growth rates (and thus will reach breeding size earlier) than those from older populations. Using a common garden design, I show that this is indeed the case: both tadpoles and juvenile toads from frontal populations grow around 30 per cent faster than those from older, long established populations. These results support theoretical predictions that r increases during range advance and highlight the importance of understanding the evolution of life history during range advance.


2021 ◽  
Author(s):  
◽  
Joe C. Gunn

The Smallmouth Bass (Micropterus dolomieu) is one of the most highly targeted sport fishes in the world. Anglers vie for the opportunity to catch Smallmouth Bass recreationally and competitively, spending billions of dollars every year on travel, equipment, and conservation permits. Along with their extreme popularity, they are of central importance in their native ecosystems throughout central and eastern North America. They are voracious apex predators, controlling top-down food web dynamics among fishes and invertebrates in both streams and natural lakes, and they act as obligate hosts in the life cycles of several freshwater mussels. A great deal is known about the general ecology of Smallmouth Bass and their role in aquatic communities across their extensive native distribution. Much less is known about levels and distribution of diversity within the species. In 1940, Carl Hubbs and Reeve Bailey published descriptions of two distinct subspecies: the Northern Smallmouth Bass (M. d. dolomieu), inhabiting the central and eastern portion of the range, and the Neosho Smallmouth Bass (M. d. velox), which is range-restricted to the Arkansas River Basin in the Central Interior Highlands. While the subspecies classification was largely accepted among taxonomists, it was predicated on only a few subtle morphological traits, including differences in coloration, body size, and the presence of glossohyal teeth. Researchers began to investigate genetic divergence among Smallmouth Bass populations at the end of the twentieth century. Some genetic structure has been detected, but the overall diversity and the evolutionary forces generating contemporary patterns have been considered extremely complex and therefore unresolved, especially where the Neosho and Northern subspecies ranges meet in the Central Interior Highlands. To address the need for a robust understanding of the divergence and evolution history of Smallmouth Bass in the Central Interior Highlands, I addressed three broad areas concerning the phylogeography and conservation of the species using a combination of morphological, genetic, and genomic data: 1) patterns of genetic and morphological differentiation between the Neosho and Northern Smallmouth Bass subspecies, 2) lineage diversification and the extent and origins of admixture within the subspecies, and 3) effects of admixture on individual growth and fitness in two streams within the Neosho Smallmouth Bass native range. Using neutral microsatellite markers and a combination of three independent Bayesian analysis methods, I detected complex and hierarchical population structure of Smallmouth Bass in the Central Interior Highlands. The broadest level of structure indicated two distinct genetic clusters corresponding to the Neosho and Northern subspecies, but with substantial and heterogenous patterns of admixture within some streams in the Neosho native range. At finer levels of structure, clusters corresponded to river drainages and to potentially distinct populations within drainages. The Northern and Neosho subspecies were morphologically distinct overall based on principal component analysis of five morphometric traits, but they significantly differed only in head length. Based on genome-wide variation at over 50,000 single nucleotide polymorphisms, the Neosho and Northern subspecies represented two diverged, monophyletic clades, each comprising two additional monophyletic lineages. Populations in Big Piney Creek and the Illinois Bayou within the Neosho range also showed signatures of local adaptation based on outlier FST analysis. Admixture in the Illinois River system within the Neosho range originated from a hatchery strain of Northern Smallmouth Bass found in Skiatook Lake, Oklahoma, while admixture in the Elk River, upper Arkansas River tributaries, and the Illinois Bayou and Big Piney Creek system originated from the White River in the Northern range. Demographic analysis revealed that admixture in these streams has occurred on different time scales, in some cases likely due to historic migration, and in other cases likely due to secondary contact, possibly as a result of anthropogenic introductions. In Big Sugar Creek and the Elk River, two Neosho Smallmouth Bass native streams known to be admixed with White River Northern Smallmouth Bass, individual growth did not differ between genetically pure Neosho, pure Northern, or admixed fish. However, in the Elk River alone, average length-at-infinity (maximum length) was lower for admixed fish than for either pure Neosho or pure Northern fish. We also found a significant negative relationship between multi-locus heterozygosity (based on fourteen microsatellite loci) and body condition, suggesting that increased intermixing may be causing outbreeding depression in these streams. The Neosho and Northern Smallmouth Bass constitute highly differentiated, locally adapted, and independently evolving lineages in the Central Interior Highlands. Despite divergence, there are also complex and extensive patterns of admixture in the Neosho range which may be contributing to lower fitness in two Neosho Smallmouth Bass streams. It will be crucial to consider these patterns and their potential outcomes in the development of management protocols for the preservation of endemic diversity within this economically and ecologically vital sportfish.


2018 ◽  
Author(s):  
Iris Wang ◽  
Nicholas Michael Michalak ◽  
Joshua Ackerman

Life history theory posits organisms face tradeoffs in how they allocate resources to reproduction, parenting, and growth. These patterns of resource allocation can be classified more broadly into life history strategies, which vary on a continuum from fast to slow. These distinctions can be applied to describe within species and between species differences. Slow strategies are marked by increased investment in growth, a delay in reproductive investment, and increased investment in parenting. In contrast, fast strategies are marked by early investment in reproduction at a cost of growth and a reduced investment in parenting in favor of further reproduction.


The Auk ◽  
2020 ◽  
Vol 137 (3) ◽  
Author(s):  
John T Rotenberry ◽  
Priya Balasubramaniam

Abstract The mass of a bird’s egg is a critical attribute of the species’ life history and represents a fundamental component of reproductive effort. Indeed, the tradeoff between the number of eggs in a clutch and clutch mass lies at the heart of understanding how environmental attributes such as nest predation or adult mortality influence reproductive investment. However, egg masses have not been reported for the majority of avian species. We capitalized on the strong allometric relationship between avian body mass and egg mass to produce egg mass estimates for over 5,500 species previously lacking such information. These estimates are accompanied by measures of the robustness of the regressions used to produce them (e.g., sample size, root mean square error [RMSE] of estimation, coefficient of determination, and degree of extrapolation), thus allowing independent evaluation of the suitability of any estimate to address a particular research question relating to avian life history. Most estimates (~5,000) were based on family-level egg mass–body mass regressions, with the remainder derived from other relationships such as ordinal regressions. We compared estimating regressions based on adult vs. female body masses and, after finding little difference between the 2, based our final estimates on adult masses as those were more numerous in the literature. What small differences between adult- and female-based regressions that did occur were not related to sexual size dimorphism across families. These new estimates, coupled with ~5,000 egg masses reported in the literature, provide a foundation of over 10,000 species for wider investigations assessing variation in reproductive effort in birds over a broad array of ecological and evolutionary contexts.


2010 ◽  
Vol 88 (9) ◽  
pp. 900-904
Author(s):  
F. Stephen Dobson ◽  
Pierre Jouventin

Williams (1966; Am. Nat. 100(916): 687–690) furthered R.A. Fisher’s concept of reproductive value by breaking it into two components: (1) current reproduction and (2) residual reproductive value (RRV, the summed product of survival and reproduction over the rest of the lifespan). He predicted a negative correlation of measures of these two components among species, and this prediction led in part to the idea of trade-offs in life-history theory. We tested Williams’ prediction with 24 species of albatrosses and petrels (order Procellariiformes), species with a great range of body sizes and all laying only one egg at a time (like humans, highly iteroparous). Two measures of reproductive investment were not negatively correlated with RRV. Adjusting data for body mass and phylogeny resulted in significant positive associations. In addition, any measure of annual parental allocation to reproduction (once adjusted for body size) should give a positive association with RRV as shown by a simple simulation model that assumes a highly iteroparous life cycle. Under such life cycles, Williams’ prediction confounds the positive influence of reproduction on both current investment and RRV. Principles of life-history theory, however, do not require re-evaluation, as this particular prediction can in at least some cases be internally inconsistent.


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