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20 results for “Musca domestica”
Figure. Mean pre-adult development time (in days) values for all strains. Vertical bars denote 0.95 confidence intervals. in Effects of artificial migration of susceptible individuals on resistance and fitness of a fenitrothion-resistant strain of Musca domestica (L.) Diptera
Figure. Mean pre-adult development time (in days) values for all strains. Vertical bars denote 0.95 confidence intervals.
Figure 4 in The predatory behavior of Hydrotaea albuquerquei (Lopes) larvae on the larvae of Musca domestica Linnaeus under laboratory conditions
Figure 4. Functional Response. The predatory capacity of H. albuquerquei larvae (predator) on Musca domestica larvae (prey) at different proportional prey densities to the total number of larvae (200 individuals) of predators and prey in other encounters. The statistical model (Poisson distribution with correction of the distribution for Quasipoisson) of the predatory capacity is in the upper portion of the graph. H1M1, H. albuquerquei first-instar larvae versus M. domestica first-instar larvae. H2M1, H. albuquerquei second-instar larvae versus M. domestica first-instar larvae. H3M1, third-instar larvae of H. albuquerquei versus first-instar larvae of M. domestica. H3M2, third-instar larvae of H. albuquerquei versus second-instar larvae of M. domestica.
Figure 3 in The predatory behavior of Hydrotaea albuquerquei (Lopes) larvae on the larvae of Musca domestica Linnaeus under laboratory conditions
Figure 3. Survival of predator (%) of Hydrotaea albuquerquei larvae (predator) at different proportional densities of prey with the total number of larvae (200 individuals) of predators and prey in other encounters. The statistical model (Binomial distribution with correction of the distribution for Quasibinomial) of the predator's survival is in the upper portion of the graph to the H1M1, H2M1 and H3M1 encounters. H1M1, H. albuquerquei first-instar larvae versus M. domestica first-instar larvae. H2M1, H. albuquerquei second-instar larvae versus M. domestica first-instar larvae. H3M1, third-instar larvae of H. albuquerquei versus first-instar larvae of M. domestica. H3M2, third-instar larvae of H. albuquerquei versus second-instar larvae of M. domestica.
Figure 2 in The predatory behavior of Hydrotaea albuquerquei (Lopes) larvae on the larvae of Musca domestica Linnaeus under laboratory conditions
Figure 2. Survival of prey (%) of Musca domestica larvae (prey) at different proportional prey densities to the total number of larvae (200 individuals) of predators and prey in other encounters. The statistical model (Binomial distribution with correction of the distribution for Quasibinomial) of the prey survival is in the upper portion of each graph. H1M1, H. albuquerquei first-instar larvae versus M. domestica first-instar larvae. H2M1, H. albuquerquei second-instar larvae versus M. domestica first-instar larvae. H3M1, third-instar larvae of H. albuquerquei versus first-instar larvae of M. domestica. H3M2, third-instar larvae of H. albuquerquei versus second-instar larvae of M. domestica.
Figure 1 in The predatory behavior of Hydrotaea albuquerquei (Lopes) larvae on the larvae of Musca domestica Linnaeus under laboratory conditions
Figure 1. Diagram showing the sampling design of the interaction of larvae of different instars (1, 2 and 3) between the predator Hydrotaea albuquerquei (H) and the prey Musca domestica (M). The other encounters (HM) considered the differences in size between the larvae of the species. In each encounter (HM) of the different instars, 200 larvae of the species were placed together in different proportions considering the ratio of M. domestica larvae (M) to eachH.albuquerquei larva (H), establishing proportional densities between predators (H) and preys (M) in agreement with Table 1. For each encounter and density, triplicates were performed.
Figure 4 in Bisexual and oedipal reproduction of Macrocheles muscaedomesticae (Acari, Macrochelidae) feeding on Musca domestica (Diptera, Muscidae) eggs
Figure 4 Age-stage-specific life expectancy (vxj) of Macrocheles muscaedomesticae feeding on Musca domestica eggs: bisexual cohort.
Figure 3 in Bisexual and oedipal reproduction of Macrocheles muscaedomesticae (Acari, Macrochelidae) feeding on Musca domestica (Diptera, Muscidae) eggs
Figure 3 Age-stage-specific life expectancy (exj) of Macrocheles muscaedomesticae feeding onMusca domestica eggs: bisexual (left) and oedipal (right) cohorts.
Figure 2 in Bisexual and oedipal reproduction of Macrocheles muscaedomesticae (Acari, Macrochelidae) feeding on Musca domestica (Diptera, Muscidae) eggs
Figure 2 Age-specific survival rate (lx), fecundity (mx) and maternity (lxmx) of Macrocheles muscaedomesticae feeding onMusca domestica
Figure 1 in Bisexual and oedipal reproduction of Macrocheles muscaedomesticae (Acari, Macrochelidae) feeding on Musca domestica (Diptera, Muscidae) eggs
Figure 1 Age-stage-specific survival rate S (xj) of Macrocheles muscaedomesticae feeding onMusca domesticaeggs: bisexual (left) and oedipal (right) cohorts.
Data from: Is multifactorial sex determination in the house fly, Musca domestica (L.), stable over time?
Sex determination pathways evolve rapidly, usually because of turnover of master regulatory genes at the top of the developmental pathway. Polygenic sex determination is expected to be a transient state between ancestral and derived conditions. However, polygenic sex determination has been observed in numerous animal species, including the house fly, Musca domestica. House fly males carry a male-determining factor (M) that can be located on any chromosome, and an individual male may have multiple M factors. Females lack M and/or have a dominant allele of the Md-tra gene(Md-traD) that acts as a female-determining locus even in the presence of multiple copies of M. We found the frequency and linkage of M in house flies collected in Chino, CA (USA) was relatively unchanged between 1982 and 2014. The frequency of females with Md-traD in the 2014 collection was 33.6% (n=140). Analysis of these results, plus previously published data, revealed a strong correlation between the frequencies of Md-traD and multiple M males, and we find that these populations are expected to have balanced sex ratios. We also find that fitness values that allow for the invasion and maintenance of multiple sex determining loci suggest that sexually antagonistic selection could be responsible for maintaining polygenic sex determination in house fly populations. The stability over time and equilibrium frequencies within populations suggest the house fly polygenic sex determination system is not in transition, and provide guidance for future investigations on the factors responsible for the polymorphism.
Data from: Benzyl alcohol synergistic effect with deltamethrin against Musca domestica with molecular docking of potential modes of action
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Data from: Microbial communities of the house fly Musca domestica vary with geographical location and habitat
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Data from: Is multifactorial sex determination in the house fly, Musca domestica (L.), stable over time?
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High-fat and high-sugar diets induce rapid adaptations of fat storage in the house fly Musca domestica L
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Impacts of the Hytrosavirus on the Transcriptome of the Housefly, Musca domestica
GEO Series GSE88939. Musca domestica. 6 samples. Type: Expression profiling by high throughput sequencing.
Transcriptome Differences between Alternative Sex Determining Genotypes in the House Fly, Musca domestica
GEO Series GSE67065. Musca domestica. 16 samples. Type: Expression profiling by high throughput sequencing.
A Whole Transcriptional Linkage Analysis of Gene Co-Regulation in Insecticide Resistant House Flies, Musca domestica
GEO Series GSE39327. Musca domestica. 4 samples. Type: Expression profiling by high throughput sequencing.
Identification of constitutively-expressed immune effectors in the house fly (Musca domestica) and the transcription factors that regulate them
GEO Series GSE182611. Musca domestica. 28 samples. Type: Expression profiling by high throughput sequencing.
Early developmental transcriptome of Musca domestica.
GEO Series GSE85160. Musca domestica. 10 samples. Type: Expression profiling by high throughput sequencing.
Function analysis and characterisation of a novel chitinase, MdCht9, in Musca domestica
GEO Series GSE189491. Musca domestica. 6 samples. Type: Expression profiling by high throughput sequencing.
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Allen Brain Atlas
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