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40 results for “post-mating”

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zenodo32/100

Figure 9 in An imperfect imago? Post-mating loss of iridescent scales in Cheimas butterflies may change female from attractive to cryptic (Lepidoptera: Nymphalidae: Satyrinae)

Figure 9. Mating simulation experiment in Cheimas opalinus dominici. (a) Female hind wing mounted; (b) male hind wing mounted on the female hind wing; (c) male hind wing artificial movement over the female hind wing; (d) faded female dorsal hind wing after removing the male wing at the end of the experiment.

opennotspecifiedApr 2018View details →
zenodo32/100

Figure 7 in An imperfect imago? Post-mating loss of iridescent scales in Cheimas butterflies may change female from attractive to cryptic (Lepidoptera: Nymphalidae: Satyrinae)

Figure 7. Scanning electron microscope photographs of Cheimas opalinus opalinus scales: (a) bluegreen (folded) and brown (flat) cover scales; (b) blue-green (folded) cover scales making up the hind wing dorsum structurally coloured patch; (c, d) microstructures of the blue-green colour-generating scale in two magnifications and different views, the periodicity of the cross ribs and the microribs on the side of the ridges are responsible; (e, f) female brown wing areas showing the scales of the hind wing dorsal surface (e) and the area of the blue patch after losing the blue colour-generating scales (f) (scale as indicated).

opennotspecifiedApr 2018View details →
zenodo32/100

Figure 2 in An imperfect imago? Post-mating loss of iridescent scales in Cheimas butterflies may change female from attractive to cryptic (Lepidoptera: Nymphalidae: Satyrinae)

Figure 2. Young females of various subspecies of Cheimas opalinus (left column: virgin, right column: mated): (a, b) C. o. dominici (El Baho); (c, d) C. o. opalinus (El Potrero); (e, f) C. o. rosalinus (Paramo El Rosal).

opennotspecifiedApr 2018View details →
dryad32/100

Data from: Population density mediates the interaction between pre- and post-mating sexual selection

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publicFeb 2018View details →
dryad32/100

Data from: Wolbachia and host intrinsic reproductive barriers contribute additively to post-mating isolation in spider mites

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publicJun 2021View details →
dryad32/100

Data from: The effects of synthetic estrogen exposure on pre-mating and post-mating episodes of selection in sex-role-reversed Gulf pipefish

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publicJul 2013View details →
dryad28/100

Data from: Multiple post-mating barriers to hybridisation in field crickets

Mechanisms that prevent different species from interbreeding are fundamental to the maintenance of biodiversity. Barriers to interspecific matings, such as failure to recognize a potential mate, are often relatively easy to identify. Those occurring after mating, such as differences in the how successful sperm are in competition for fertilisations, are cryptic and have the potential to create selection on females to mate multiply as a defence against maladaptive hybridization. Cryptic advantages to conspecific sperm may be very widespread and have been identified based on the observations of higher paternity of conspecifics in several species. However, a relationship between the fate of sperm from two species within the female and paternity has never been demonstrated. We use competitive microsatellite PCR to show that in two hybridising cricket species, Gryllus bimaculatus and G. campestris, sequential cryptic reproductive barriers are present. In competition with heterospecifics, more sperm from conspecific males is stored by females. Additionally, sperm from conspecific males has a higher fertilisation probability. This reveals that conspecific sperm precedence can occur through processes fundamentally under the control of females, providing avenues for females to evolve multiple mating as a defence against hybridization, with the counterintuitive outcome that promiscuity reinforces isolation and may promote speciation.

opencc-zeroDec 2011View details →
dryad28/100

Data from: The relationship between post-mating reproductive isolation and reinforcement in Phlox

The process of speciation involves the accumulation of reproductive isolation (RI) between diverging lineages. Selection can favor increased RI via the process of reinforcement, whereby costs to hybridization impose selection for increased prezygotic RI. Reinforcement results in phenotypic divergence within at least one taxon, as a result of costly hybridization between sympatric taxa. The strength of selection driving reinforcement is determined by the cost of hybridization and the frequency of hybridization. We investigated the cost of hybridization by quantifying post-mating RI barriers among Phlox species that comprise one of the best-studied cases of reinforcement. We determined if the strength of RI differs among lineages that have and have not undergone reinforcement, how much variability there is within species in RI, and whether RI is associated with phylogenetic relatedness. We found high RI for the species that underwent phenotypic divergence due to reinforcement; however, RI was also high between other species pairs. We found extensive variability in RI among individuals within species, and no evidence that the strength of RI was associated with phylogenetic relatedness. We suggest that phenotypic divergence due to reinforcement is associated with the frequency of hybridization and introgression, and not the cost of hybridization in this clade.

opencc-zeroDec 2017View details →
dryad28/100

Data from: The relationship between post-mating reproductive isolation and reinforcement in Phlox

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publicMay 2018View details →
dryad28/100

Data from: Multiple biological mechanisms result in correlations between pre- and post-mating traits that differ among versus within individuals and genotypes

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publicJul 2018View details →
dryad28/100

Data from: Divergence in sex peptide-mediated female post-mating responses in Drosophila melanogaster

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publicAug 2018View details →
dryad28/100

Data from: Variation in the post-mating fitness landscape in fruitflies

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publicApr 2017View details →
dryad28/100

Data from: Macronutrients and micronutrients drive trade-offs between male pre- and post-mating sexual traits

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publicJul 2019View details →
dryad28/100

Data from: Multiple post-mating barriers to hybridisation in field crickets

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publicDec 2012View details →
geo24/100

Roles of female and male genotype in post-mating responses in Drosophila melanogaster

GEO Series GSE104706. Drosophila melanogaster. 90 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenOct 2017View details →
geo24/100

Seminal fluid components alone stimulate post-mating changes in honey bee queens (Apis mellifera)

GEO Series GSE145395. Apis mellifera carnica. 38 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenJul 2020View details →
zenodo20/100

Figure 1 in An imperfect imago? Post-mating loss of iridescent scales in Cheimas butterflies may change female from attractive to cryptic (Lepidoptera: Nymphalidae: Satyrinae)

Figure 1. Young males of various subspecies of Cheimas opalinus from various localities: (a) C. o. opalinus (La Culata); (b) C. o. opalinus (El Potrero); (c) C. o. cristalinus (Pico Tonojo); (d) C. o. cristalinus (Pico Tonojo); (e) C. opalinus cristalinus (Agua de Obispo); (f) C. opalinus iosephi (Quebrada El Cahote).

opennotspecifiedApr 2018View details →
geo16/100

Regulation of Anopheles gambiae male accessory gland genes influences post-mating response in female

GEO Series GSE27233. Anopheles gambiae. 6 samples. Type: Expression profiling by array.

openGEO-OpenFeb 2013View details →
geo12/100

Post-mating expression of female D. melanogaster genomes experimentally evolved under different post-copulatory sexual selection regimes

GEO Series GSE30089. Drosophila melanogaster. 32 samples. Type: Expression profiling by array.

openGEO-OpenJan 2014View details →
geo12/100

Post-mating expression of female Drosophila melanogaster genomes experimentally evolved under different post-copulatory sexual selection regimes

GEO Series GSE48385. Drosophila melanogaster. 32 samples. Type: Expression profiling by array.

openGEO-OpenJan 2014View details →

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International Brain Laboratory public data

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Last verified 2026-04-29Open record