The cost of reproduction to the clonal herb Asarum canadense (wild ginger)

1995 ◽  
Vol 73 (10) ◽  
pp. 1683-1686 ◽  
Author(s):  
Angela M. Muir
Keyword(s):  
Sexual Reproduction ◽  
Asexual Reproduction ◽  
Energy Cost ◽  
Reproductive Effort ◽  
Cost Of Reproduction ◽  
Net Energy ◽  
Subsequent Growth ◽  
Subsequent Storage ◽  
The Cost ◽  
And Storage

The cost of reproduction to the clonal understorey herb Asarum canadense (wild ginger) was examined by measuring subsequent growth and storage. All connected vegetative rhizome was controlled and fully measured. Three important aspects of reproductive effort were addressed: (i) the effect of sexual reproduction on subsequent storage and growth of fragments, (ii) the effect of asexual reproduction on subsequent storage and growth of fragments, and (iii) a comparison to determine the least costly method of reproduction. It was found that sexual reproduction in wild ginger has an energy cost that diverts energy from storage and growth. Asexual reproduction represents neither a net energy cost nor gain to the fragment and is the least costly mode of reproduction to wild ginger. Key words: Asarum canadense, reproduction, rhizome, clonal.

The cost of reproduction in women: Reproductive effort and oxidative stress in premenopausal and postmenopausal American women

2017 ◽  
Vol 30 (1) ◽  
pp. e23069 ◽  
Author(s):  
Anna Ziomkiewicz ◽  
Amara Frumkin ◽  
Yawei Zhang ◽  
Amelia Sancilio ◽  
Richard G. Bribiescas
Keyword(s):  
Oxidative Stress ◽  
Reproductive Effort ◽  
Cost Of Reproduction ◽  
American Women ◽  
The Cost ◽  
And Oxidative Stress

Freshwater Migration as a Determinant Factor in the Somatic Cost of Reproduction of Two Anadromous Coregonines of James Bay

1990 ◽  
Vol 47 (2) ◽  
pp. 318-334 ◽  
Author(s):  
Yvan Lambert ◽  
Julian J. Dodson
Keyword(s):  
Energy Cost ◽  
Reproductive Effort ◽  
Energy Content ◽  
Cost Of Reproduction ◽  
Energy Gain ◽  
Lake Whitefish ◽  
James Bay ◽  
Energy Increase ◽  
Species Specific ◽  
Somatic Energy

We tested the hypothesis that the species-specific costs of migration differentially affect reproductive effort and somatic cost of reproduction in sympatric anadromous populations of cisco (Coregonus artedii) and lake whitefish (C. clupeaformis) of James Bay. Reproductive effort, which includes the energy cost of migration, is higher for cisco. Female cisco allocate more energy to reproduction than its total energy gain. The energy invested by lake whitefish in reproduction is approximately equal to its seasonal energy gain. Reproduction results in large differences in the energy content of gonads, viscera, and carcass between reproductive and nonreproductive fish of the same length. Neither cisco nor lake whitefish are able to spawn two years in succession. The somatic energy increase of reproductive female cisco is 121% lower than the somatic energy increase of nonreproductive females; similar comparisons are 89% (female) and 103% (male) for lake whitefish. The energy cost of migration is largely responsible for the higher somatic cost of reproduction observed for cisco. These different somatic costs of migration are related to resource accumulation prior to migration and to differences in the aerobic cost of swimming between the two species in combination with the difficulty of the freshwater migration.

Life histories of North American game birds: a reanalysis

1988 ◽  
Vol 66 (8) ◽  
pp. 1906-1912 ◽  
Author(s):  
Todd W. Arnold
Keyword(s):  
Life History ◽  
North American ◽  
Life Histories ◽  
Life History Traits ◽  
Reproductive Effort ◽  
Cost Of Reproduction ◽  
Reproductive Value ◽  
Trade Offs ◽  
Game Birds ◽  
The Cost

Recently, Zammuto (R. M. Zammuto. 1986. Can. J. Zool. 64: 2739–2749) suggested that North American game birds exhibited survival–fecundity trade-offs consistent with the "cost of reproduction" hypothesis. However, there were four serious problems with the data and the analyses that Zammuto used: (i) the species chosen for analysis ("game birds") showed little taxonomic or ecological uniformity, (ii) the measures of future reproductive value (maximum longevity) were severely biased by unequal sample sizes of band recoveries, (iii) the measures of current reproductive effort (clutch sizes) were inappropriate given that most of the birds analyzed produce self-feeding precocial offspring, and (iv) the statistical units used in the majority of analyses (species) were not statistically independent with respect to higher level taxonomy. After correcting these problems, I found little evidence of survival–fecundity trade-offs among precocial game birds, and I attribute most of the explainable variation in life-history traits of these birds to allometry, phylogeny, and geography.

scholarly journals Evidence for the Cost of Reproduction in Humans: High Lifetime Reproductive Effort Is Associated with Greater Oxidative Stress in Post-Menopausal Women

PLoS ONE ◽  
2016 ◽  
Vol 11 (1) ◽  
pp. e0145753 ◽  
Author(s):  
Anna Ziomkiewicz ◽  
Amelia Sancilio ◽  
Andrzej Galbarczyk ◽  
Magdalena Klimek ◽  
Grazyna Jasienska ◽  
...  
Keyword(s):  
Oxidative Stress ◽  
Reproductive Effort ◽  
Cost Of Reproduction ◽  
Menopausal Women ◽  
Post Menopausal ◽  
The Cost

Energy cost of square dancing

1975 ◽  
Vol 38 (1) ◽  
pp. 44-45 ◽  
Author(s):  
M. Jette ◽  
H. Inglis
Keyword(s):  
Energy Cost ◽  
American Heart Association ◽  
American Heart ◽  
Average Energy ◽  
Heart Association ◽  
Work Load ◽  
Functional Class ◽  
Net Energy ◽  
Class 1 ◽  
The Cost

This experiment was concerned with determining the energy cost of two popular Western square dancing routines: the “Mish-Mash,” which is a relatively fast-moving dance with quick movements, and the “Singing” dance, which is a slower and more deliberate type of dance. The subjects were four middle-aged couples, veteran members of a local square dancing club. Sitting and standing pulmonary ventilations were determined through the use of the Tissot gasometer. Kofranyi-Michaelis respirometers were employed for the dance routine ventilations. These apparatus were fitted with a Monoghan neoprene cushion plastic mask. Gas samples were collected in polyethylene metallized bags and analyzed for O2 and CO2 content. The net energy cost for the two dances was appropriately summarized. The results indicated that for the males the net average energy cost of the “Mish-Mash,” dance was 0.085 and 0.077 kcal/min per kg for the “Singing” dance. For the females, the cost was 0.088 and 0.084 kcal/min per kg, respectively. A net average cost of these two dances yielded a caloric expenditure of 5.7 kcal/min for a 70-kg male and 5.2 kcal/min for a 60-kg female. It was indicated that during the course of a typical square dance evening, a 70-kg man would expend some 425 kcal. while a 60-kg female would burn some 390 kcal. The energy cost of the dances studied were determined to be within the permissible work load of a functional class 1 patient with diseases of the heart as determined by the American Heart Association.

Infectious diseases, reproductive effort and the cost of reproduction in birds

1997 ◽  
pp. 53-61 ◽  
Author(s):  
L. Gustafsson ◽  
D. Nordling ◽  
M. S. Andersson ◽  
B. C. Sheldon ◽  
A. Qvarnström
Keyword(s):  
Infectious Diseases ◽  
Reproductive Effort ◽  
Cost Of Reproduction ◽  
The Cost

Molecular basis of adaptive evolution of sperm motility involved in in vivo fertilization of terrestrial animals

Impact ◽  
2020 ◽  
Vol 2020 (6) ◽  
pp. 73-75
Author(s):  
Akihiko Watanabe
Keyword(s):  
Sexual Reproduction ◽  
Sperm Motility ◽  
Asexual Reproduction ◽  
Acrosome Reaction ◽  
Sperm Morphology ◽  
Adaptive Potential ◽  
Selective Pressures ◽  
The Face ◽  
Genetic Profiles

One of the unifying traits of life on this planet is reproduction, or life's ability to make copies of itself. The mode of reproduction has evolved over time, having almost certainly begun with simple asexual reproduction when the ancestral single celled organism divided into two. Since these beginnings' life has tried out numerous strategies, and perhaps one of the most important and successful has been sexual reproduction. This form of reproduction relies on the union of gametes, otherwise known as sperm and egg. Evolutionarily, sexual reproduction allows for greater adaptive potential because the genes of two unique individuals have a chance to recombine and mix in order to produce a new individual. Unlike asexual reproduction which produces genetically-identical clones of the parent individual, sex produces offspring with novel genes and combinations of genes. Therefore, in the face of new selective pressures there is a higher chance that one of these novel genetic profiles will produce an adaptation that is advantageous in the new circumstances. Dr Akihiko Watanabe is a reproductive biologist based in the Department of Biology, Faculty of Science Yamagata University in Japan, he is currently working on three research projects; a comparative study on the signalling pathways for inducing sperm motility and acrosome reaction in amphibians, the mechanism behind the adaptive modification of sperm morphology and motility, and the origin of sperm motility initiating substance (SMIS).

scholarly journals The Advantages of Segregation and the Evolution of Sex

Genetics ◽  
2003 ◽  
Vol 164 (3) ◽  
pp. 1099-1118 ◽  
Author(s):  
Sarah P Otto
Keyword(s):  
Sexual Reproduction ◽  
Asexual Reproduction ◽  
Deleterious Mutations ◽  
Evolution Of Sex ◽  
Beneficial Mutations ◽  
Selection Regime ◽  
Strong Selection ◽  
Genome Wide ◽  
Low Levels

AbstractIn diploids, sexual reproduction promotes both the segregation of alleles at the same locus and the recombination of alleles at different loci. This article is the first to investigate the possibility that sex might have evolved and been maintained to promote segregation, using a model that incorporates both a general selection regime and modifier alleles that alter an individual’s allocation to sexual vs. asexual reproduction. The fate of different modifier alleles was found to depend strongly on the strength of selection at fitness loci and on the presence of inbreeding among individuals undergoing sexual reproduction. When selection is weak and mating occurs randomly among sexually produced gametes, reductions in the occurrence of sex are favored, but the genome-wide strength of selection is extremely small. In contrast, when selection is weak and some inbreeding occurs among gametes, increased allocation to sexual reproduction is expected as long as deleterious mutations are partially recessive and/or beneficial mutations are partially dominant. Under strong selection, the conditions under which increased allocation to sex evolves are reversed. Because deleterious mutations are typically considered to be partially recessive and weakly selected and because most populations exhibit some degree of inbreeding, this model predicts that higher frequencies of sex would evolve and be maintained as a consequence of the effects of segregation. Even with low levels of inbreeding, selection is stronger on a modifier that promotes segregation than on a modifier that promotes recombination, suggesting that the benefits of segregation are more likely than the benefits of recombination to have driven the evolution of sexual reproduction in diploids.

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