A preliminary study of variation and inheritance of life-history traits and the occurrence of hybrid vigour in Sitobion avenae (F.) (Hemiptera: Aphididae)

1988 ◽  
Vol 78 (1) ◽  
pp. 75-83 ◽  
Author(s):  
Chris Newton ◽  
A. F. G. Dixon

AbstractClones of Sitobion avenae (F.) collected in southern England in 1983 and 1984 were subjected to sexual-inducing conditions in the laboratory (12 L:8 D photoperiod at 15°C and/or 8 L:16 D photoperiod at 12°C). Most clones were continuously parthenogenetic under these conditions; some clones produced males only (androcyclic), and the same behaviour was observed under field conditions in the autumn of 1983. In contrast, over 90% of the clones collected from Scotland in 1984 were holocyclic (i.e. cyclically parthenogenetic). Fundatrices from intra- and interclonal matings were obtained. Those from interclonal matings were significantly more fecund than fundatrices from intraclonal matings. Examination of the descendants of these fundatrices indicated that both life-history strategy and migratory tendency were genetically-determined.

2020 ◽  
Vol 40 (1) ◽  
pp. 39-47 ◽  
Author(s):  
Chen Luo ◽  
Lucie S. Monticelli ◽  
Dandan Li ◽  
Syed Suhail Ahmed ◽  
Gaurav Pandharikar ◽  
...  

2019 ◽  
Vol 22 (1) ◽  
pp. 56-64 ◽  
Author(s):  
Xiangli Xu ◽  
Xiaoxia Liu ◽  
Qingwen Zhang ◽  
Junxiang Wu

Life history traits were evaluated in the wing polyphenic aphid, Sitobion avenae (Fabricius), by rearing the winged and wingless morphs under the laboratory conditions. Winged morph with large thoraces exhibited a significantly greater morphological investment in flight apparatus than wingless morph with small thoraces. Compared to the winged morph, the wingless morph produced significantlymore nymphs and exhibited significantly faster nymph development rates. In addition, the age at which reproduction first occurred for the winged morph was significantly delayed, and higher mortality was recorded.The results suggest that the fitness differences associated with wingsmay be related to nymph development, adult fecundity, and mortality. Based on these results, the trends and exceptions of life history traits for the wing polyphenic insects are discussed.


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 ◽  
...  

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.


2016 ◽  
Vol 371 (1690) ◽  
pp. 20150187 ◽  
Author(s):  
Daniel Sol ◽  
Ferran Sayol ◽  
Simon Ducatez ◽  
Louis Lefebvre

The evolutionary origin of innovativeness remains puzzling because innovating means responding to novel or unusual problems and hence is unlikely to be selected by itself. A plausible alternative is considering innovativeness as a co-opted product of traits that have evolved for other functions yet together predispose individuals to solve problems by adopting novel behaviours. However, this raises the question of why these adaptations should evolve together in an animal. Here, we develop the argument that the adaptations enabling animals to innovate evolve together because they are jointly part of a life-history strategy for coping with environmental changes. In support of this claim, we present comparative evidence showing that in birds, (i) innovative propensity is linked to life histories that prioritize future over current reproduction, (ii) the link is in part explained by differences in brain size, and (iii) innovative propensity and life-history traits may evolve together in generalist species that frequently expose themselves to novel or unusual conditions. Combined with previous evidence, these findings suggest that innovativeness is not a specialized adaptation but more likely part of a broader general adaptive system to cope with changes in the environment.


1997 ◽  
Vol 75 (6) ◽  
pp. 954-958 ◽  
Author(s):  
Roger Fons ◽  
Françoise Poitevin ◽  
Josette Catalan ◽  
Henri Croset

Populations of the lesser white-toothed shrew, Crocidura suaveolens (Pallas, 1811), from Corsica show an increase in adult body size associated with a decrease in litter size. The average number of embryos in wild Corsican females is smaller (mean 2.6, n = 62) than in mainland females (mean 4.6, n = 173). A breeding experiment was run for 4 years, yielding three generations. Under standard breeding conditions, the differences between island and mainland populations were maintained and were significant (median litter size was 2 for Corsica and 5 for the mainland). These differences in life-history traits were therefore proved experimentally to be genetically determined. Hypotheses concerning the mechanisms responsible for these differences are discussed.


2020 ◽  
Author(s):  
Rebecca Sear

Interest in incorporating life history research from evolutionary biology into the human sciences has grown rapidly in recent years. Two core features of this research have the potential to prove valuable in strengthening theoretical frameworks in the health and social sciences: the idea that these is a fundamental trade-off between reproduction and health; and that environmental influences are important in determining individual life histories. For example, the idea that mortality risk in the environment shifts individuals along a ‘fast-slow continuum’ of ‘life history strategy’ is now popular in the evolutionary human sciences. In biology, ‘fast’ life history strategists prioritise reproduction over health so that individuals grow quickly, reproduce early and often, and suffer a rapid deterioration in health and relatively early death; ‘slow’ strategists start reproducing later, have fewer offspring, and die at an older age. Evolutionary human scientists tend to assume that, along with these life history outcomes, several behavioural traits, such as parenting, mating and risk-taking behaviour and, in the most expansive version, a whole suite of psychological and personality traits also cluster together into ‘fast’ and ‘slow’ life histories. Here, I review the different approaches to life history strategies from evolutionary anthropologists, developmental psychologists and evolutionary psychologists, in order to assess the theoretical and empirical evidence for human ‘life history strategies’. While there is precedent in biology for the argument that some behavioural traits, notably risk-taking behaviour, may be linked in predictable ways with life history outcomes, there is relatively little theoretical or empirical justification for including a very wide range of behavioural traits in a ‘life history strategy’. Given the diversity and lack of consistency in this human life history literature, I then make recommendations for improving its usefulness: 1) greater clarity over terminology, so that a distinction is made between life history outcomes such as age at maturity, first birth and death, and behavioural traits which may be associated with life history outcomes but are not life history traits themselves; 2) more empirical data on linkages between life history traits, behavioural traits and the environment, including the underlying mechanisms which generate these linkages; 3) more empirical work on life history strategies in a much broader range of populations than has so far been studied. Such a research programme on human life history has the potential to produce valuable insights for the health and social sciences, not least because of its interest in environmental influences on health, reproduction and behaviour.


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