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36 results for “Musca”
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.
Fig. 1 in Phoresy of a sucking louse, Linognathus sp. (Phthiraptera: Anoplura: Linognathidae), by Musca (Byomya) conducens Walker (Diptera: Muscidae) in South Africa
Fig. 1. Photograph of the phoretic Linognathus sp. (Anoplura, Linognathidae) attached to the right mid tarsus of Musca conducens Walker (Muscidae).
Figs 1–4 in The kleptoparasitic habits of Musca albina Wiedemann, 1830 (Diptera: Muscidae)
Figs 1–4. Kleptoparasitic Musca albina Wiedemann females: (1) perching near dung-rolling Scarabaeus (numerous individuals were observed perching near active scarabs, but none were observed to alight in the vicinity of source dung); (2) cluster on rapidly sinking dung ball (during the brief period the host scarab spends interring the dung ball the kleptoparasitic muscids arrive and swiftly oviposit); (3) single female with her ovipositor inserted into a partially buried dung ball; (4) female flies only alight on fully formed Scarabaeus dung balls, and only when stationary (no muscids were observed on actively rolling dung balls); artificially impeding motion of the ball by impaling it with a twig lured in this female.
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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Fig. 4 in Biotransformation of betulinic acid by Circinella muscae and Cunninghamella echinulata to discover anti-inflammatory derivatives
Fig. 4. Inhibition against NO production of betulinic acid, 1–4, and 7–10 in LPS-induced RAW 264.7 cells.
FIGURES 4–8. Cheiloceps musca Uhler, cotype. 4 in To the revision of the genus Thionia Stål (Hemiptera, Fulgoroidea, Issidae), with description of new genera and new subtribe
FIGURES 4–8. Cheiloceps musca Uhler, cotype. 4—dorsal view; 5—lateral view; 6—frontal view; 7—ovipositor, lateral view; 8—labels.
FIGURES 27–29 in External ultrastructure of Progonoia diatreta sp. nov. (Bacillariophyta, Scoliotropidaceae) differs from P. musca and P. intercedens comb. nov.
FIGURES 27–29. Progonoia diatreta, sp. nov., internal SEM. 27. General view of valve. 28. Detail of apex showing terminal raphe ending and internal aspect of alveoli, with partial transverse walls and a series of small pores around the inner edge of one, the outer edge of the other, and the apical end of the last alveolus (arrow). Some of the pores of the external surface can be seen where the inner membrane has broken away (arrowhead). 29. Detail of central area showing the double helictoglossa (arrow) and the partial transverse walls extending into each alveolus from the longitudinal wall (arrowhead). Scale bars: Fig. 27 = 10 μm, Figs 28, 29 = 2 μm.
FIGURES 7–13 in External ultrastructure of Progonoia diatreta sp. nov. (Bacillariophyta, Scoliotropidaceae) differs from P. musca and P. intercedens comb. nov.
FIGURES 7–13. Progonoia intercedens, LM (Figs 7–10 DIC) and external SEM (Figs 11–13). 7, 8. Oblique frustule at two focal planes. 9. Valve. 10. Frustule in girdle view, showing the striae on the copulae. 11. Valve, external view. 12. Detail of areolae showing contrasting structure of longitudinal rows: a hymen near the surface in the middle rows (arrowhead), probably unbroken in life, and the deeper pits of the inner and marginal areolae (arrows). Notice also the small pores with structure similar to the middle rows. 13. Detail of marginal areolae, showing the deeper membranes with small marginal perforations (arrow). Scale bars: Figs 7–10 = 10 μm, Fig. 11 = 5 μm, Figs 12, 13 = 1 μm.
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.