Life-history traits of a small-bodied coastal shark

2013 ◽  
Vol 64 (1) ◽  
pp. 54 ◽  
Author(s):  
Adrian N. Gutteridge ◽  
Charlie Huveneers ◽  
Lindsay J. Marshall ◽  
Ian R. Tibbetts ◽  
Mike B. Bennett
Keyword(s):  
Life History ◽  
Life Histories ◽  
Life History Traits ◽  
Logistic Function ◽  
Early Maturation ◽  
Large Size ◽  
History Of ◽  
Age Model ◽  
Best Fit ◽  
Combined Data

The life histories of small-bodied coastal sharks, particularly carcharhinids, are generally less conservative than those of large-bodied species. The present study investigated the life history of the small-bodied slit-eye shark, Loxodon macrorhinus, from subtropical Hervey Bay, Queensland, and compared this species' biology to that of other coastal carcharhinids. The best-fit age model provided parameters of L∞ = 895 mm total length (TL), k = 0.18 and t0 = –6.3 for females, and L∞ = 832 mm TL, k = 0.44 and t0 = –2.6 for males. For sex-combined data, a logistic function provided the best fit, with L∞ = 842 mm TL, k = 0.41 and α = –2.2. Length and age at which 50% of the population was mature was 680 mm TL and 1.4 years for females, and 733 mm TL and 1.9 years for males. Within Hervey Bay, L. macrorhinus exhibited an annual seasonal reproductive cycle, producing an average litter of 1.9 ± 0.3 s.d. With the exception of the low fecundity and large size at birth relative to maximum maternal TL, the life-history traits of L. macrorhinus are comparable to other small-bodied coastal carcharhinids, and its apparent fast growth and early maturation contrasts that of large-bodied carcharhinids.

Coevolutionary interactions between host life histories and parasite life cycles

Parasitology ◽  
1998 ◽  
Vol 116 (S1) ◽  
pp. S47-S55 ◽  
Author(s):  
J. C. Koella ◽  
P. Agnew ◽  
Y. Michalakis
Keyword(s):  
Life History ◽  
Life Cycle ◽  
Life Histories ◽  
Life History Traits ◽  
Evolutionary Ecology ◽  
Life Cycles ◽  
Microsporidian Parasite ◽  
History Of ◽  
Host Life ◽  
Host Parasite

SummarySeveral recent studies have discussed the interaction of host life-history traits and parasite life cycles. It has been observed that the life-history of a host often changes after infection by a parasite. In some cases, changes of host life-history traits reduce the costs of parasitism and can be interpreted as a form of resistance against the parasite. In other cases, changes of host life-history traits increase the parasite's transmission and can be interpreted as manipulation by the parasite. Alternatively, changes of host's life-history traits can also induce responses in the parasite's life cycle traits. After a brief review of recent studies, we treat in more detail the interaction between the microsporidian parasite Edhazardia aedis and its host, the mosquito Aedes aegypti. We consider the interactions between the host's life-history and parasite's life cycle that help shape the evolutionary ecology of their relationship. In particular, these interactions determine whether the parasite is benign and transmits vertically or is virulent and transmits horizontally.Key words: host-parasite interaction, life-history, life cycle, coevolution.

scholarly journals Life in the Slow Lane: Reproductive Life History of the White-Browed Scrubwren, an Australian Endemic

The Auk ◽  
2000 ◽  
Vol 117 (2) ◽  
pp. 479-489 ◽  
Author(s):  
Robert D. Magrath ◽  
Ashley W. Leedman ◽  
Janet L. Gardner ◽  
Anthony Giannasca ◽  
Anjeli C. Nathan ◽  
...  
Keyword(s):  
Life History ◽  
Life Histories ◽  
Life History Traits ◽  
Life History Strategy ◽  
Breeding Biology ◽  
Long Period ◽  
Successful Attempt ◽  
Reproductive Life ◽  
History Of ◽  
Small Clutch

Abstract An understanding of geographic and phylogenetic variation in passerine life histories is hampered by the scarcity of studies from the Southern Hemisphere. We documented the breeding biology of the White-browed Scrubwren (Sericornis frontalis), an Australia endemic in the Pardalotidae (parvorder Corvida). Like other members of the Pardalotidae, scrubwrens had a long laying interval (two days), a long incubation period (declining from 21 to 17 days through the season), and a long period of postfledging parental care (6 to 7 weeks). Scrubwrens appeared to be typical of the Australian Corvida in having a small clutch size (three eggs) and a long breeding season (5.4 months), and they also had a long interval between breeding attempts (10 days after a failed attempt, 21 days after a successful attempt). Scrubwrens were multibrooded, often raising two broods successfully and occasionally raising three broods. The breeding biology of scrubwrens adds further support to claims of a distinct life-history strategy for members of the Corvida but also reinforces evidence that some “Corvida” life-history traits more specifically are those of the Pardalotidae.

Hormones and Behavior

2019 ◽  
pp. 11-26
Author(s):  
Maren N. Vitousek ◽  
Laura A. Schoenle
Keyword(s):  
Life History ◽  
Life Histories ◽  
Life History Traits ◽  
Developmental Plasticity ◽  
Endocrine System ◽  
Phenotypic Traits ◽  
Social Environments ◽  
Trade Offs ◽  
And Behavior

Hormones mediate the expression of life history traits—phenotypic traits that contribute to lifetime fitness (i.e., reproductive timing, growth rate, number and size of offspring). The endocrine system shapes phenotype by organizing tissues during developmental periods and by activating changes in behavior, physiology, and morphology in response to varying physical and social environments. Because hormones can simultaneously regulate many traits (hormonal pleiotropy), they are important mediators of life history trade-offs among growth, reproduction, and survival. This chapter reviews the role of hormones in shaping life histories with an emphasis on developmental plasticity and reversible flexibility in endocrine and life history traits. It also discusses the advantages of studying hormone–behavior interactions from an evolutionary perspective. Recent research in evolutionary endocrinology has provided insight into the heritability of endocrine traits, how selection on hormone systems may influence the evolution of life histories, and the role of hormonal pleiotropy in driving or constraining evolution.

A comparative study of the life histories of Nematodirus battus and N. filicollis, nematode parasites of sheep

Parasitology ◽  
1959 ◽  
Vol 49 (3-4) ◽  
pp. 374-386 ◽  
Author(s):  
R. J. Thomas
Keyword(s):  
Life History ◽  
Intestinal Mucosa ◽  
Related Species ◽  
Life Histories ◽  
Basic Pattern ◽  
Culture Methods ◽  
Closely Related Species ◽  
Nematode Parasites ◽  
History Of ◽  
Comparative Description

1. The life history of N. battus is described, and a comparative description of the life history of N. filicollis is given.2. The life histories of these two species are compared with those of N. spathiger and N. helvetianus, two closely related species, and are shown to follow the same basic pattern, with minor variations in timing which appear to be specific in nature, and not related to differences in culture methods or host species.3. The pathogenesis of Nematodirus species is discussed and related to the migration of larvae into the intestinal mucosa during development.

III.—The Life-history and Cytology of Didymium nigripes Fr.

1932 ◽  
Vol 57 (1) ◽  
pp. 93-142 ◽  
Author(s):  
Elsie J. Cadman
Keyword(s):  
Life History ◽  
Life Histories ◽  
Important Research ◽  
Great Work ◽  
Animal Kingdom ◽  
History Of ◽  
Natural Groups

Since 1860, in which year De Bary published his great work Die Mycetozoen, the investigation of the life-history of members of the Mycetozoa has aroused a considerable amount of interest, and a great deal of important research has been carried out in this connection. The group of organisms is particularly interesting, because it lies on the borderline between plant and animal kingdoms, and it is very possible that a detailed investigation of several species of the Mycetozoa might be of considerable assistance in elucidating certain obscure points in the life-histories of higher members of both the great natural groups. The term “Mycetozoa,” which we owe to De Bary, will be used throughout in preference to the older term “Myxogastres” invented by Fries (32, p. 2), and that of “Myxomycetes” first employed by Link (32, p. 2). “Mycetozoon,” or “fungus-like animal,” is a very appropriate description of a member of the group, since during part of its life-history it exhibits distinctly animal-like characters, and the individuals move rapidly by means of flagella, whilst later, during the development of the sporangium, a plant-like form is assumed. The combination of plant and animal characters has given rise to much discussion as to the position of the Mycetozoa in plant or animal kingdom, and the group has been claimed by both zoologists and botanists.

A Primer of Life Histories

2021 ◽  
Author(s):  
Jeffrey A. Hutchings
Keyword(s):  
Life History ◽  
Life Histories ◽  
Life History Theory ◽  
Life History Traits ◽  
Reproductive Effort ◽  
Effective Means ◽  
Academic Experience ◽  
Sustainable Exploitation ◽  
Evolution Of Life ◽  
Opportune Time

Life histories describe how genotypes schedule their reproductive effort throughout life in response to factors that affect their survival and fecundity. Life histories are solutions that selection has produced to solve the problem of how to persist in a given environment. These solutions differ tremendously within and among species. Some organisms mature within months of attaining life, others within decades; some produce few, large offspring as opposed to numerous, small offspring; some reproduce many times throughout their lives while others die after reproducing just once. The exponential pace of life-history research provides an opportune time to engage and re-engage new generations of students and researchers on the fundamentals and applications of life-history theory. Chapters 1 through 4 describe the fundamentals of life-history theory. Chapters 5 through 8 focus on the evolution of life-history traits. Chapters 9 and 10 summarize how life-history theory and prediction has been applied within the contexts of conservation and sustainable exploitation. This primer offers an effective means of rendering the topic accessible to readers from a broad range of academic experience and research expertise.

scholarly journals The application of life history information to the conservation management of Chrysoritis butterflies (Lepidoptera: Lycaenidae) in South Africa

Koedoe ◽  
2004 ◽  
Vol 47 (1) ◽  
Author(s):  
R.F. Terblanche ◽  
H. Van Hamburg
Keyword(s):  
South Africa ◽  
Life History ◽  
Life Histories ◽  
Host Plants ◽  
Conservation Management ◽  
Aesthetic Value ◽  
Wing Patterns ◽  
In The Wild ◽  
History Of ◽  
Voucher Specimens

Due to their intricate life histories and the unique wing patterns and colouring the butterflies of the genus Chrysoritis are of significant conservation and aesthetic value. Thisoverview probes into practical examples of butterfly life history research applicable to environmental management of this relatively well-known invertebrate group in South Africa. Despite the pioneer work on life histories of Chrysoritis in the past, more should be done to understand the life history of the butterflies in the wild, especially their natural host plants and the behaviour of adults and larvae. A system of voucher specimens of host plants should be introduced in South Africa. Although various host plant species in nature are used by the members of Chrysoritis, including the Chrysoritis chrysaor group, the choice of these in nature by each species is significant for conservation management and in the case of Chrysoritis aureus perhaps even as a specific characteristic.A revision of the ant genus Crematogaster will benefit the conservation management of Chrysoritis species since some of these ant species may consist of a number of specieswith much more restricted distributions than previously thought. Rigorous quantified tudies of population dynamics of Chrysoritis butterflies are absent and the introductionof such studies will benefit conservation management of these localised butterflies extensively.

Long-bone development and life-history traits of the Devonian tristichopterid Hyneria lindae

2018 ◽  
Vol 109 (1-2) ◽  
pp. 75-86 ◽  
Author(s):  
Viktoriia KAMSKA ◽  
Edward B. DAESCHLER ◽  
Jason P. DOWNS ◽  
Per E. AHLBERG ◽  
Paul TAFFOREAU ◽  
...  
Keyword(s):  
Life History ◽  
Limb Development ◽  
Life History Traits ◽  
Bone Development ◽  
Bone Histology ◽  
Long Bone ◽  
General Character ◽  
Appendicular Skeleton ◽  
Predatory Behaviour ◽  
Large Size

ABSTRACTHyneria lindae is one of the largest Devonian sarcopterygians. It was found in the Catskill Formation (late Famennian) of Pennsylvania, USA. The current study focuses on the palaeohistology of the humerus of this tristichopterid and supports a low ossification rate and a late ossification onset in the appendicular skeleton. In addition to anatomical features, the large size of the cell lacunae in the cortical bone of the humerus mid-shaft may suggest a large genome size and associated neotenic condition for this species, which could, in turn, be a partial explanation for the large size of H. lindae. The low metabolism of H. lindae revealed here by bone histology supports the hypothesis of an ambush predatory behaviour. Finally, the lines-of-arrested-growth pattern and late ossification of specimen ANSP 21483 suggest that H. lindae probably had a long juvenile stage before reaching sexual maturity. Although very few studies address the life-history traits of stem tetrapods, they all propose a slow limb development for the studied taxa despite different ecological conditions and presumably distinct behaviours. The bone histology of H. lindae would favour the hypothesis that a slow long-bone development could be a general character for stem tetrapods.

Life on the edge: the ecology and life history of the tropidurine iguanid lizard Uranoscodon superciliosum

1990 ◽  
Vol 68 (7) ◽  
pp. 1366-1373 ◽  
Author(s):  
Jeffrey M. Howland ◽  
Laurie J. Vitt ◽  
Pamela T. Lopez
Keyword(s):  
Life History ◽  
Social Interaction ◽  
Sexual Dimorphism ◽  
Small Diameter ◽  
Habitat Specialization ◽  
Large Size ◽  
Tropical Wet Forest ◽  
History Of ◽  
Forest Streams ◽  
Small Forest

An Amazonian population of the iguanid lizard Uranoscodon superciliosum was studied in lowland tropical wet forest in central Pará, Brazil. These nonheliothermic lizards are restricted to densely vegetated habitats near (often over) water, particularly riverbanks and small forest streams, where they utilize small-diameter perches and feed on a wide variety of invertebrates, apparently at the water's edge. They mature at moderate to large size at an age of about 1.5 years. Production of moderate-sized clutches of eggs is seasonal, and reproduction and fat storage both cycle in association with rainfall and flooding. Although they occur in fairly high densities, social interaction is uncommon and sexual dimorphism is not pronounced. The ecology and life history of this lizard seem to be strongly influenced by the unusual habitat specialization.

scholarly journals Density Dependence, Evolutionary Optimization, and the Diversification of Avian Life Histories

The Condor ◽  
2000 ◽  
Vol 102 (1) ◽  
pp. 9-22 ◽  
Author(s):  
Robert E. Ricklefs
Keyword(s):  
Life History ◽  
Life Table ◽  
Life Histories ◽  
Life History Traits ◽  
Evolutionary Ecology ◽  
Reproductive Rate ◽  
Empirical Modeling ◽  
Adult Survival ◽  
Life History Variation ◽  
Evolutionary Response

Abstract Although we have learned much about avian life histories during the 50 years since the seminal publications of David Lack, Alexander Skutch, and Reginald Moreau, we still do not have adequate explanations for some of the basic patterns of variation in life-history traits among birds. In part, this reflects two consequences of the predominance of evolutionary ecology thinking during the past three decades. First, by blurring the distinction between life-history traits and life-table variables, we have tended to divorce life histories from their environmental context, which forms the link between the life history and the life table. Second, by emphasizing constrained evolutionary responses to selective factors, we have set aside alternative explanations for observed correlations among life-history traits and life-table variables. Density-dependent feedback and independent evolutionary response to correlated aspects of the environment also may link traits through different mechanisms. Additionally, in some cases we have failed to evaluate quantitatively ideas that are compelling qualitatively, ignored or explained away relevant empirical data, and neglected logical implications of certain compelling ideas. Comparative analysis of avian life histories shows that species are distributed along a dominant slow-fast axis. Furthermore, among birds, annual reproductive rate and adult mortality are directly proportional to each other, requiring that pre-reproductive survival is approximately constant. This further implies that age at maturity increases dramatically with increasing adult survival rate. The significance of these correlations is obscure, particularly because survival and reproductive rates at each age include the effects of many life-history traits. For example, reproductive rate is determined by clutch size, nesting success, season length, and nest-cycle length, each of which represents the outcome of many different interactions of an individual's life-history traits with its environment. Resolution of the most basic issues raised by patterns of life histories clearly will require innovative empirical, modeling, and experimental approaches. However, the most fundamental change required at this time is a broadening of the evolutionary ecology paradigm to include a variety of alternative mechanisms for generating patterns of life-history variation.

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