Relevant bibliographies by topics / Flies DIPTERA

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Flies DIPTERA'

Author: Grafiati
Published: 4 June 2021
Last updated: 9 February 2022

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Journal articles on the topic "Flies DIPTERA"

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Yarger, Alexandra M., Katherine A. Jordan, Alexa J. Smith, and Jessica L. Fox. "Takeoff diversity in Diptera." Proceedings of the Royal Society B: Biological Sciences 288, no. 1942 (2021): 20202375. http://dx.doi.org/10.1098/rspb.2020.2375.

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The order Diptera (true flies) are named for their two wings because their hindwings have evolved into specialized mechanosensory organs called halteres. Flies use halteres to detect body rotations and maintain stability during flight and other behaviours. The most recently diverged dipteran monophyletic subsection, the Calyptratae, is highly successful, accounting for approximately 12% of dipteran diversity, and includes common families like house flies. These flies move their halteres independently from their wings and oscillate their halteres during walking. Here, we demonstrate that this subsection of flies uses their halteres to stabilize their bodies during takeoff, whereas non-Calyptratae flies do not. We find that flies of the Calyptratae are able to take off more rapidly than non-Calyptratae flies without sacrificing stability. Haltere removal decreased both velocity and stability in the takeoffs of Calyptratae, but not other flies. The loss of takeoff velocity following haltere removal in Calyptratae (but not other flies) is a direct result of a decrease in leg extension speed. A closely related non-Calyptratae species ( D. melanogaster ) also has a rapid takeoff, but takeoff duration and stability are unaffected by haltere removal. Haltere use thus allows for greater speed and stability during fast escapes, but only in the Calyptratae clade.
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Adler, Peter, and Gregory Courtney. "Ecological and Societal Services of Aquatic Diptera." Insects 10, no. 3 (2019): 70. http://dx.doi.org/10.3390/insects10030070.

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More than any other group of macro-organisms, true flies (Diptera) dominate the freshwater environment. Nearly one-third of all flies—roughly 46,000 species—have some developmental connection with an aquatic environment. Their abundance, ubiquity, and diversity of adaptations to the aquatic environment position them as major drivers of ecosystem processes and as sources of products and bioinspiration for the benefit of human society. Larval flies are well represented as ecosystem engineers and keystone species that alter the abiotic and biotic environments through activities such as burrowing, grazing, suspension feeding, and predation. The enormous populations sometimes achieved by aquatic flies can provide the sole or major dietary component for other organisms. Harnessing the services of aquatic Diptera for human benefit depends on the ingenuity of the scientific community. Aquatic flies have played a role as indicators of water quality from the earliest years of bioassessment. They serve as indicators of historical and future ecological and climate change. As predators and herbivores, they can serve as biological control agents. The association of flies with animal carcasses in aquatic environments provides an additional set of tools for forensic science. The extremophilic attributes of numerous species of Diptera offer solutions for human adaptation to harsh terrestrial and extraterrestrial environments. The potential pharmaceutical and industrial applications of the symbiotic microbial community in extremophilic Diptera are better explored than are those of dipteran chemistry. Many flies provide valuable ecological and human services as aquatic immatures, but are also pests and vectors of disease agents as terrestrial adults. The scientific community, thus, is challenged with balancing the benefits and costs of aquatic Diptera, while maintaining sustainable populations as more species face extinction.
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Reilly, Lucy A., Joana Favacho, Lourdes M. Garcez, and Orin Courtenay. "Preliminary evidence that synanthropic flies contribute to the transmission of trachoma- causing Chlamydia trachomatis in Latin America." Cadernos de Saúde Pública 23, no. 7 (2007): 1682–88. http://dx.doi.org/10.1590/s0102-311x2007000700020.

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Synanthropic flies have been shown to be important mechanical vectors of Chlamydia trachomatis, which causes trachoma. However entomological studies have not been forthcoming in Latin America. This study assesses the relationship between household dipteran fly densities and active childhood trachoma in a village on Marajó Island, Pará state, Brazil. For 78 households, members were examined for signs of trachoma, relative abundance of potential trachoma vectors (Diptera, Chloropidae and Diptera, Muscidae) was quantified by trap counts, and additional measures of household hygiene associated with C. trachomatis transmission were assessed. Active childhood trachoma prevalence was 24.1% (45/187), present in 46.2% of sampled households with evidence of case clustering. Childhood prevalence was positively associated with increased fly densities, whereas indirect measures of sanitary conditions (latrine ownership and perceived importance of flies) showed a protective effect. This study indicates that C. trachomatis can be transmitted by synanthropic flies in this region of Latin America.
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Deguenon, Jean M., Jiwei Zhu, Steven Denning, Michael H. Reiskind, David W. Watson, and R. Michael Roe. "Control of Filth Flies, Cochliomyia macellaria (Diptera: Calliphoridae), Musca domestica (Diptera: Muscidae), and Sarcophaga bullata (Diptera: Sarcophagidae), Using Novel Plant-Derived Methyl Ketones." Journal of Medical Entomology 56, no. 6 (2019): 1704–14. http://dx.doi.org/10.1093/jme/tjz107.

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AbstractFilth flies live in close proximity to humans and livestock and transmit pathogens. Current control relies on chemical insecticides, and flies can develop resistance to these insecticides. The public is also interested in natural and safer insecticides. Therefore, alternative pesticides compatible with the synanthropic nature of flies are needed. Four plant aliphatic methyl ketones were evaluated for control of adult house flies, Musca domestica L., blow flies, Cochliomyia macellaria (F.), and gray flesh flies, Sarcophaga bullata (Parker). In sealed petri dish assays, 2-heptanone, 2-octanone, 2-nonanone, and 2-undecanone exhibited fumigant activity against house flies with 24-h LC50s of 6.9, 7.5, 8.0, and 9.2 µg/cm3, respectively. Further research focused on undecanone (a U.S. EPA-registered biopesticide). When tested in larger enclosures at 1.7, 2.3, and 2.8 µg/cm3, undecanone provided 60.4, 82.2, and 94.4% house fly mortality; 56.9, 75.6, and 92.5% flesh fly mortality; and 62.1, 84.5, and 97.9% blow fly mortality, respectively, after a 2-h exposure. In a two-choice behavioral assay with 194.6 µg/cm2 of the test compound on the treatment versus an untreated surface of the same area, the overall mean repellencies for blow flies were 84.7% for undecanone versus 87.6% for N,N-diethyl-meta-toluamide (DEET). For house flies, mean repellencies were 80.7% for undecanone and 84.9% for DEET. The house fly topical LD50 for undecanone was 58.1 µg per fly. Undecanone was far less expensive for filth fly control than the gold standard for insect fumigation, methyl bromide.
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Boppre, Michael, and Brian R. Pitkin. "Attraction of Chloropid Flies to Pyrrolizidine Alkaloids (Diptera: Chloropidae)." Entomologia Generalis 13, no. 1-2 (1988): 81–85. http://dx.doi.org/10.1127/entom.gen/13/1988/81.

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Frantsevich, Leonid, and Ludmilla Frantsevich. "Der Mittelhüft-Fortsatz von Fliegen (Diptera: Brachycera)." Entomologia Generalis 23, no. 4 (1999): 233–50. http://dx.doi.org/10.1127/entom.gen/23/1999/233.

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EL-HAWAGRY, MAGDI S. "Catalogue of Egyptian Tephritoidea (Diptera: Schizophora: Acalyptratae)." Zootaxa 4299, no. 2 (2017): 151. http://dx.doi.org/10.11646/zootaxa.4299.2.1.

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All known Egyptian taxa of the superfamily Tephritoidea are systematically catalogued. Synonymies, type localities, type depositories, world distributions by biogeographic realm(s) and country, Egyptian localities and dates of collection for Egyptian tephritoid species are provided. The known Egyptian host plants of phytophagous species are listed. A total number of 86 tephritoid species belonging to 48 genera, 15 tribes, 9 subfamilies, and repre-senting 6 families has been catalogued. The treated families are: Lonchaeidae (lance flies), Piophilidae (skippers), Platystomatidae (signal flies), Pyrgotidae (pyrgotid flies), Tephritidae (fruit flies) and Ulidiidae (picture–winged flies).
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Williams, K. A., and M. H. Villet. "Spatial and Seasonal Distribution of Forensically Important Blow Flies (Diptera: Calliphoridae) in Makhanda, Eastern Cape, South Africa." Journal of Medical Entomology 56, no. 5 (2019): 1231–38. http://dx.doi.org/10.1093/jme/tjz056.

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AbstractThe seasonal activity of adults of eight forensically important blow fly species [Calliphora croceipalpis (Diptera: Calliphoridae), Jaennicke, Lucilia sericata (Meigen) (Diptera: Calliphoridae), L. cuprina (Wiedemann) (Diptera: Calliphoridae), Chrysomya chloropyga (Wiedemann) (Diptera: Calliphoridae), Ch. albiceps (Wiedemann) (Diptera: Calliphoridae), Ch. marginalis (Wiedemann) (Diptera: Calliphoridae), Ch. putoria (Wiedemann) (Diptera: Calliphoridae), Ch. megacephala (Fabricius) (Diptera: Calliphoridae)] was quantified from collections in Makhanda, South Africa. Flies were collected in traps baited with chicken liver and placed in the field at eight locations for four consecutive days each fortnight for 14 mo. The seasonal distribution of each species compared well to published seasonal distributions of these blow flies elsewhere in South Africa, with evidence of year-to-year variation within seasons that might be explained by weather. This information is important for determining when and where certain species are likely to occur and will be of use in forensic investigations and myiasis management plans.
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Sontowski, Rebekka, and Nicole M. van Dam. "Functional Variation in Dipteran Gut Bacterial Communities in Relation to Their Diet, Life Cycle Stage and Habitat." Insects 11, no. 8 (2020): 543. http://dx.doi.org/10.3390/insects11080543.

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True flies and mosquitos (Diptera) live in habitats and consume diets that pose specific demands on their gut bacterial communities (GBCs). Due to diet specializations, dipterans may have highly diverse and species-specific GBCs. Dipterans are also confronted with changes in habitat and food sources over their lifetime, especially during life history processes (molting, metamorphosis). This may prevent the development of a constant species- or diet-specific GBC. Some dipterans are vectors of several human pathogens (e.g., malaria), which interact with GBCs. In this review, we explore the dynamics that shape GBC composition in some Diptera species on the basis of published datasets of GBCs. We thereby focus on the effects of diet, habitats, and life cycle stages as sources of variation in GBC composition. The GBCs reported were more stage-specific than species- or diet-specific. Even though the presence of GBCs has a large impact on the performance of their hosts, the exact functions of GBCs and their interactions with other organisms are still largely unknown, mainly due to the low number of studies to date. Increasing our knowledge on dipteran GBCs will help to design pest management strategies for the reduction of insecticide resistance, as well as for human pathogen control.
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Nartshuk, Emilia. "Chloropid flies (Diptera, Chloropidae) of Cyprus." Entomologica Fennica 1, no. 4 (1990): 227–32. http://dx.doi.org/10.33338/ef.83489.

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A small collection of chloropids collected by H. Lindberg on Cyprus in 1939 contains 18 species. Speccafrons cypria sp. n. is described. A lectotype is designated for Scoliophthalmus trapezoides Becker. Most of the species have a Mediterranean distribution.
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Dissertations / Theses on the topic "Flies DIPTERA"

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Swink, Whitney Garland. "The Dance Flies (Diptera: Empidoidea) of Madagascar." NCSU, 2009. http://www.lib.ncsu.edu/theses/available/etd-10302009-191803/.

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The Empidoidea are a monophyletic superfamily of flies that includes dance flies (Empididae), long-legged flies (Dolichopodidae), and several small families (Atelestidae, Hybotidae, and Brachystomatidae). Empidoids are found worldwide and contain many thousands of species, but none have ever been described from Madagascar. An ongoing biodiversity survey by the California Academy of Sciences has brought to light many hundreds of undescribed empidoids from the island. This research project involves description, databasing, and DNA barcoding to establish the first estimates of empidoid species diversity in Madagascar. This study will contribute to critical surveys of species richness for rapidly degrading habitats in this important biodiversity hotspot. Representatives from two empidoid families, Empididae and Hybotidae were collected from Madagascar. There are eight new species of Hybos (Hybotidae: Hybotinae) from Madagascar: H. gardneri sp. nov., H. flaviarticulus sp. nov., H. verykoukis sp. nov., H. fianarantsoensis sp. nov., H. exastis sp. nov., H. triangulus sp. nov., H. angustifacies sp. nov., and H. ignotopalpus sp. nov. All species are described and male genitalia are illustrated. DNA barcoding was performed on the flies from the subfamily Hybotinae in order to infer species limits, but due to poorly preserved or degraded DNA, no definitive conclusions could be drawn. To aid identification, eight new barcodes were obtained that will be submitted to the barcode library upon publication of the new species. All data collected for the Madagascar empidoids have been recorded in a Mandala database and all images have been uploaded into Morphbank. Additionally, a LucID key is available on the Internet for species identification.
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Torr, Stephen J. "The host-orientated behaviour of tsetse flies (Diptera: Glossinidae)." Thesis, Imperial College London, 1987. http://hdl.handle.net/10044/1/46793.

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Campbell-Lendrum, Diarmid H. "Factors affecting rates of predation on tsetse (Diptera: Glossinidae)." Thesis, University of Oxford, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.260118.

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Weldon, Christopher W. "Dispersal and mating behaviour of Queensland fruit fly, Bactrocera tryoni (Froggatt) (Diptera: Tephritidae) : implications for population establishment and control /." Connect to full text, 2005. http://setis.library.usyd.edu.au/adt/public_html/adt-NU/public/adt-NU20051007.085638.

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Whittington, Andrew Eric. "Taxonomic revision of the Afrotropical Plastotephritinae (Diptera; Platystomatidae)." Thesis, University of Aberdeen, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.324145.

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Schulz, Katja-Sabine. "The evolution of mating systems in black scavenger flies (Diptera: Sepsidae)." Diss., The University of Arizona, 1999. http://hdl.handle.net/10150/289010.

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Black scavenger flies are characterized by sexual behaviours that are very unusual in insects. I have studied two of the most remarkable elements of their mating systems: the timing of copulations immediately after an oviposition bout (post-oviposition matings) and the males' escorting of ovipositing females. In a study of the patterns of sperm precedence in one sepsid species, I found that the sepsids' peculiar timing of matings is not associated with unusual patterns of sperm precedence: sepsid males displace rival sperm and achieve a large last male advantage, which is the most common outcome of sperm competition in insects. I discuss the potential significance of sperm transfer mechanisms for the sepsids' timing of matings, and I consider factors that may favour the maintenance of post-oviposition matings in sepsid populations. In a survey of sepsid mating patterns, I found that post-oviposition matings are typical of many black scavenger flies and that mating systems characterized by the absence of copulations with gravid females may have arisen early in the family's evolutionary history. In several black scavenger flies, ovipositing females are commonly accompanied by an escorting male, and in all but one of the species I have studied, escorting is pre-copulatory. In several species, I found pronounced geographic variation in the expression of this trait. I argue that sepsids share certain characteristics which may have facilitated multiple independent origins of escorting behaviour. In order to investigate the adaptive significance of escorting, I have conducted a comparative study of patterns of sexual size dimorphism and sex ratios at oviposition sites in conspecific populations that show great divergence in the expression of this trait. The results of this research support the pre-copulatory mate guarding hypothesis for the adaptive significance of escorting behaviour, and they suggest that conspecific populations vary significantly in the degree or nature of sexual selection acting both on morphology and behaviour of males. Furthermore, in a study of the genetic architecture of escorting behaviour, I found that the observed behavioural variation has a genetic basis: the expression of escorting behaviour is a quantitative trait with a significant sex-related component of inheritance.
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Cotton, S. "The signalling function of eyespan in stalk-eyed flies (Diptera: Diopsidae)." Thesis, University College London (University of London), 2004. http://discovery.ucl.ac.uk/1446601/.

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Genetic models of the handicap theory of sexual selection propose that ornaments signal heritable male quality, so females mating with the most ornamented males acquire fitness benefits for their offspring. Male ornaments are predicted to have coevolved with female preference to be larger, and so more costly. The key prediction made by the handicap hypothesis is that male sexual traits have evolved heightened condition dependence, a result of the higher differential cost of ornaments relative to other traits. I investigated evidence for condition-dependent sexual ornaments and found little support from well-designed experiments. Most studies had neglected to 1) compare condition dependence in sexual traits with suitable non-sexual controls, 2) adequately account for body size variation, and 3) assess individuals under a range of stresses representative of those experienced in nature. There was also a dearth of experimental studies exploring the genetic basis of condition dependence. I used experiments with stalk-eyed flies to examine predictions made by condition-dependent handicap models of sexual selection. Cyrtodiopsis dalmanni is highly sexually dimorphic for eyespan, and females exhibit strong mating preferences for males with large eyespans. Condition was varied experimentally by manipulating larval food availability. I found that male eyespan was more sensitive to changes in condition than female eyespan and other non-sexual traits. Male eyespan also showed a great increase in standardized phenotypic variance under stress, unlike non-sexual traits. These patterns persisted before and after controlling for body size. In contrast, there was no heightened condition dependence of male eyespan in Sphyracephala beccarri, a species without female mate choice for exaggerated male eyespan and only minor sex differences in eyespan. The genetic basis of ornament condition dependence was investigated in C. dalmanni by comparing the performance of distinct genotypes (inbred lines) along a gradient of environmental stress. Lines that produced a large ornament in one environment tended to do so in others. Stress also amplified these differences between genotypes leading to an increase in the genetic variance of the male ornament. Such patterns were less marked in non-sexual traits, and persisted after controlling for size. I looked for positive correlations between ornaments and viability by assessing the genetic correlations between male eyespan expression and four components of fitness (male fertility, female fecundity, and male and female longevity). I found no evidence that females obtain genetic benefits, other than male attractiveness, for their offspring by mating with well-ornamented males. However, body size-corrected male eyespan was negatively correlated with female longevity. This was unexpected and does not provide support for "good genes" benefits of sexual selection. Possible reasons for such findings (or lack thereof) are discussed.
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Camp, Jeremy Vann. "Host attraction and host selection in the family Corethrellidae (Wood and Borkent) (Diptera)." Click here to access thesis, 2006. http://www.georgiasouthern.edu/etd/archive/fall2006/jeremy_v_camp/camp_jeremy_v_200608_ms.pdf.

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Thesis (M.S.)--Georgia Southern University, 2006.<br>"A dissertation submitted to the Graduate Faculty of Georgia Southern University in partial fulfillment of the requirements for the degree Master of Science" ETD. Includes bibliographical references (p. 64-68) and appendix.
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Murray, Rosalind L. "The ecology and evolution of female-specific ornamentation in the dance flies (Diptera: Empidinae)." Thesis, University of Stirling, 2015. http://hdl.handle.net/1893/22157.

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Elaborate morphological ornaments can evolve if they increase the reproductive success of the bearer during competition for mates. However, ornament evolution is incredibly rare in females, and the type and intensity of selection required to develop female-specific ornamentation is poorly understood. The main goals of my thesis are to clarify the relationship between the type and intensity of sexual selection that drives the evolution of female ornamentation, and investigate alternative hypotheses that might be limiting or contributing to the development of female ornaments. I investigated the ecology and evolution of female-specific ornaments within and between species of dance flies from the subfamily Empidinae (Diptera: Empididae). The dance flies display incredible mating system diversity including those with elaborate female-specific ornaments, lek-like mating swarms, aerial copulation and nuptial gift giving. To elucidate the form of sexual selection involved in female-ornament evolution, I experimentally investigated the role of sexual conflict in the evolution of multiple female- specific ornaments in the species Rhamphomyia longicauda. Through manipulative field experiments, I found that variation in the attractiveness of two ornaments displayed by females indicates that sexual conflict, causing a coevolutionary arms race, is an important force in the evolution of multiple extravagant female ornaments. Using R. longicauda again, I tested for a role of functional load-lifting constraints on the aerial mating ability of males who paired with females displaying multiple large ornaments. I found no evidence of functional constraints influencing the mating opportunities of elaborately ornate females, but instead discovered a relationship consistent with positive assortative mating for mass. Biased sex ratios are predicted to increase the intensity of sexual selection in a population, which in turn, is predicted to influence the evolution of ornamentation. I measured the incidence and prevalence of vertically transmitted symbiotic bacteria that has been observed to distort the sex ratio in other Dipteran hosts. While my survey revealed that symbionts occur at high incidence and variable prevalence across dance fly hosts, I found no effect of symbiont infection levels on population sex ratios, or female- specific ornament evolution. Further investigation into the relationship between sex ratios and female-ornament evolution using the comparative method revealed that the operational sex ratio (OSR) of a population did not predict continuous measures of female ornamentation across species. However, female-ornament evolution did predict male relative testis investment across species indicating that female ornaments likely indicate increased levels of polyandry. My thesis reveals that sexual selection theory developed to describe male-specific ornament evolution cannot readily be translated to apply to females. I show that male mate choice, rather than functional constraints or ecological associations with bacteria, is likely driving the evolution of female-specific ornaments. I also identify sexual conflict as an important selective force in the evolution of female-specific ornaments.
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Gouge, Dawn Heather. "Biological control of sciarid flies (Diptera: Sciaridae) with entomopathogenic nematodes (Nematoda: Rhabditida), including reference to other diptera." Thesis, University of Reading, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.385057.

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Books on the topic "Flies DIPTERA"

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Weinberg, Medeea. Diptera Asilidae. Schweizerischen Entomologischen Gesellschaft, 1995.

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Royal Entomological Society of London., ed. Tachinid flies: Diptera: Tachinidae. Royal Entomological Society of London, 1993.

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Beshovski, Venelin Lazarov. Carnoidea insecta: Diptera, diptera brachycera acaliptratae. Prof. Marin Drinov Academic Publishing House, 2013.

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Miller, Sara Swan. Flies: From flower flies to mosquitoes. F. Watts, 1998.

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Geiger, Willy. Diptera Limoniidae. Insecta Helvetica, Entomolog. Institut der ETH, 1986.

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Flies eat poop! PowerKids Press, 2014.

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Kapoor, Vijay Chandra. Indian fruit flies: Insecta, Diptera, Tephritidae. Oxford & IBH Pub. Co. Pvt., 1993.

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Disney, R. H. L. Scuttle flies: Diptera (Phoridae, genus Megaselia). Royal Entomological Society of London, 1989.

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Pechuman, L. L. The Horse flies and Deer flies of Maine (Diptera, Tabanidae). Maine Agricultural and Forest Experiment Station, University of Maine, 1996.

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Remm, H. Eesti sääriksääsklased (Diptera, Tipulidae). Eesti NSV Teaduste Akadeemia, Eesti Looduseuurijate Selts, 1986.

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Book chapters on the topic "Flies DIPTERA"

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Krafsur, E. S., R. D. Moon, R. Albajes, et al. "Flies (Diptera)." In Encyclopedia of Entomology. Springer Netherlands, 2008. http://dx.doi.org/10.1007/978-1-4020-6359-6_3838.

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Wall, Richard, and David Shearer. "Adult flies (Diptera)." In Veterinary Entomology. Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-011-5852-7_4.

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Kriska, György. "True Flies – Diptera." In Freshwater Invertebrates in Central Europe. Springer Vienna, 2013. http://dx.doi.org/10.1007/978-3-7091-1547-3_22.

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Krafsur, E. S., R. D. Moon, R. Albajes, et al. "Fruit Flies (Diptera: Tephritidae)." In Encyclopedia of Entomology. Springer Netherlands, 2008. http://dx.doi.org/10.1007/978-1-4020-6359-6_3902.

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Heppner, John B., David B. Richman, Steven E. Naranjo, et al. "Scuttle Flies, (Diptera: Phoridae)." In Encyclopedia of Entomology. Springer Netherlands, 2008. http://dx.doi.org/10.1007/978-1-4020-6359-6_4093.

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Leppla, Norman C., Bastiaan M. Drees, Allan T. Showler, et al. "Robber Flies (Diptera: Asilidae)." In Encyclopedia of Entomology. Springer Netherlands, 2008. http://dx.doi.org/10.1007/978-1-4020-6359-6_3421.

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Berry, Colin, Jason M. Meyer, Marjorie A. Hoy, et al. "Black Flies (Diptera: Simuliidae)." In Encyclopedia of Entomology. Springer Netherlands, 2008. http://dx.doi.org/10.1007/978-1-4020-6359-6_361.

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Currie, Douglas C., and D. Bruce Hunter. "Black Flies (Diptera: Simuliidae)." In Parasitic Diseases of Wild Birds. Wiley-Blackwell, 2009. http://dx.doi.org/10.1002/9780813804620.ch31.

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O’Hara, James E., Igor UsUpensky, N. J. Bostanian, et al. "Tachinid Flies (Diptera: Tachinidae)." In Encyclopedia of Entomology. Springer Netherlands, 2008. http://dx.doi.org/10.1007/978-1-4020-6359-6_2344.

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Capinera, John L., Thomas O. Crist, John B. Heppner, et al. "Horse Flies and Deer Flies (Diptera: Tabanidae)." In Encyclopedia of Entomology. Springer Netherlands, 2008. http://dx.doi.org/10.1007/978-1-4020-6359-6_1401.

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Conference papers on the topic "Flies DIPTERA"

1

Doud, Carl W. "Development of stable flies and house flies (Diptera: Muscidae) in dewatered sewage biosolids." In 2016 International Congress of Entomology. Entomological Society of America, 2016. http://dx.doi.org/10.1603/ice.2016.108899.

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2

Lessard, Bryan D. "Reconstructing the phylogeny of the soldier flies (Diptera: Stratiomyidae)." In 2016 International Congress of Entomology. Entomological Society of America, 2016. http://dx.doi.org/10.1603/ice.2016.95469.

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3

Nartshuk, E. P. "Brachypterous and apterous species of grass flies (Diptera, Chloropidae)." In XI Всероссийский диптерологический симпозиум (с международным участием). Русское энтомологическое общество, 2020. http://dx.doi.org/10.47640/978-5-00105-586-0_2020_152.

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4

Cohen, Chris M. "Searching for venom: Comparative transcriptomics in robber flies (Diptera: Asilidae)." In 2016 International Congress of Entomology. Entomological Society of America, 2016. http://dx.doi.org/10.1603/ice.2016.111536.

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5

Justin Talley, Greta Schuster, David Parker, Bill Clymer, and Carl Patrick. "Monitoring Population Trends of House Flies and Stable Flies (Diptera: Muscidae) on Texas High Plains Feedlots." In 2002 Chicago, IL July 28-31, 2002. American Society of Agricultural and Biological Engineers, 2002. http://dx.doi.org/10.13031/2013.10508.

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6

Owings, Charity G. "Mediators of population genetic structure in Indiana blow flies (Diptera: Calliphoridae)." In 2016 International Congress of Entomology. Entomological Society of America, 2016. http://dx.doi.org/10.1603/ice.2016.107639.

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7

Williams, Kirstin A. "Nocturnal oviposition in forensically important flies (Diptera: Calliphoridae) in South Africa." In 2016 International Congress of Entomology. Entomological Society of America, 2016. http://dx.doi.org/10.1603/ice.2016.111029.

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8

Solecki, Anna M. "Ecophylogenetics of flies (Diptera) in a subarctic site, Churchill (MB, Canada)." In 2016 International Congress of Entomology. Entomological Society of America, 2016. http://dx.doi.org/10.1603/ice.2016.115181.

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9

Ostrovsky, A. M. "To the fauna of robber flies (Diptera, Asilidae) of SouthEastern Belarus." In XI Всероссийский диптерологический симпозиум (с международным участием). Русское энтомологическое общество, 2020. http://dx.doi.org/10.47640/978-5-00105-586-0_2020_168.

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10

Shcherbakov, M. V. "To the study of tephritid fruit-flies (Diptera, Tephritidae) of Tuva." In XI Всероссийский диптерологический симпозиум (с международным участием). Русское энтомологическое общество, 2020. http://dx.doi.org/10.47640/978-5-00105-586-0_2020_260.

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