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841 results for “fruit flies”

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zenodo28/100

Figure 3. K in Microsatellite based genetic diversity of Mediterranean fruit fly (Ceratitis capitata, Diptera: Tephritidae) populations from Southwest Turkey

Figure 3. K = 4 clustering assignment depending on the Bayesian method under an admixture model obtained by Structure software. Individuals are represented by a vertical line and each color indicates a different cluster. 1: Muğla; 2: Aydın; 3: Antalya; 4: İzmir; 5: Adana; 6: Yalova; 7: Mersin.

opencc-by-4.0Apr 2022View details →
zenodo28/100

Fig. 3 in Efficacy Of Protein Bait Sprays In Controlling Fruit Flies (Diptera: Tephritidae) Infesting Angled Luffa And Bitter Gourd In Thailand

Fig. 3. Percentage of infested fruits of angled luffa in plots treated with Pinnacle bait and untreated. (Only Bactrocera cucurbitae and B. tau were found.)

opencc-by-4.0Dec 2003View details →
zenodo28/100

FIGURES 56 in New species and new records of fruit flies of tribe Acanthonevrini (Diptera: Tephritidae: Phytalmiinae) from India

FIGURES 56. Habitus (dorsal) of male of Phorelliosoma hilaratum Hering.

opennotspecifiedSep 2024View details →
zenodo28/100

FIGURE 39 in New species and new records of fruit flies of tribe Acanthonevrini (Diptera: Tephritidae: Phytalmiinae) from India

FIGURE 39. Habitus (lateral view) of female of Erectovena desperata (Hering).

opennotspecifiedSep 2024View details →
zenodo28/100

FIGURE 1 in New species and new records of fruit flies of tribe Acanthonevrini (Diptera: Tephritidae: Phytalmiinae) from India

FIGURE 1. Dorsal habitus of female of Ptilona confracta David & Hancock, sp. n

opennotspecifiedSep 2024View details →
zenodo28/100

Linked collectors and determiners for: Royal Museum of Central Africa - True Fruit Flies (Diptera, Tephritidae) of the Afrotropical Region (ENBI wp13).

Natural history specimen data linked to collectors and determiners held within, "Royal Museum of Central Africa - True Fruit Flies (Diptera, Tephritidae) of the Afrotropical Region (ENBI wp13)". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/b276cb50-d3ea-11dc-ab69-b8a03c50a862">https://bionomia.net/dataset/b276cb50-d3ea-11dc-ab69-b8a03c50a862</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/b276cb50-d3ea-11dc-ab69-b8a03c50a862">https://gbif.org/dataset/b276cb50-d3ea-11dc-ab69-b8a03c50a862</a>. Formatted as a Frictionless Data package.

opencc-zeroJan 2024View details →
dryad28/100

Data from: Sexual harassment induces a temporary fitness cost but does not constrain the acquisition of environmental information in fruit flies

Across animals, sexual harassment induces fitness costs for females and males. However, little is known about the cognitive costs involved, i.e. whether it constrains learning processes, which could ultimately affect an individual's fitness. Here we evaluate the acquisition of environmental information in groups of fruit flies challenged with various levels of male sexual harassment. We show that, although high sexual harassment induces a temporary fitness cost for females, all fly groups of both sexes exhibit similar levels of learning. This suggests that, in fruit flies, the fitness benefits of acquiring environmental information are not affected by the fitness costs of sexual harassment, and that selection may favour cognition even in unfavourable social contexts. Our study provides novel insights into the relationship between sexual conflicts and cognition and the evolution of female counterstrategies against male sexual harassment.

opencc-zeroDec 2014View details →
dryad28/100

Data from: Exposure to males, but not receipt of sex peptide, accelerates functional aging in female fruit flies

Increased exposure to males can affect females negatively, reducing female lifespan and fitness. These costs could derive from increased mating rate and also harassment by males. Additionally, early investment in reproduction can increase the onset or rate of senescence in reproductive traits. Hence, there is a tight link between reproduction and aging. Here, we assess how mating and encounter rate with males impacts declines in female functional traits that are not directly involved in reproduction. In Drosophila melanogaster fruit flies, exposure to males and mating reduces female lifespan through harassment and receipt of seminal proteins, including sex peptide. We manipulated the intensity of female exposure to males and regularly assessed female stress responses and recorded physiological traits over her lifetime. Both mating itself and increased exposure to males accelerates declines in female climbing ability and starvation resistance. However, this is not related to changes in female body mass or fat storage. Moreover, these declines are not driven by the receipt of sex peptide. Our results suggest some synchrony in senescence across traits in response to female exposure to males, however this is not universal, as we did not find this for physiological traits. Synchrony in senescence has been theorised but little supported in the literature. It is clear that aging is a multifaceted trait; to understand environmental impacts on aging rates we must measure more than lifespan, and indeed measure senescence in multiple traits. Specifically, our work shows that we must identify which female traits are sensitive to elevated mating activity to understand the impact of antagonistic interactions between the sexes on female aging patterns.

opencc-zeroDec 2018View details →
dryad28/100

Data from: Fruit flies diversify their offspring in response to parasite infection

The evolution of sexual reproduction is often explained by Red Queen dynamics: Organisms must continually evolve to maintain fitness relative to interacting organisms, such as parasites. Recombination accompanies sexual reproduction and helps diversify an organism's offspring, so that parasites cannot exploit static host genotypes. Here we show that Drosophila melanogaster plastically increases the production of recombinant offspring after infection. The response is consistent across genetic backgrounds, developmental stages, and parasite types but is not induced after sterile wounding. Furthermore, the response appears to be driven by transmission distortion rather than increased recombination. Our study extends the Red Queen model to include the increased production of recombinant offspring and uncovers a remarkable ability of hosts to actively distort their recombination fraction in rapid response to environmental cues.

opencc-zeroDec 2014View details →
zenodo28/100

Figure 23 in New country records, annotated checklist and key to the dacine fruit flies (Diptera: Tephritidae: Dacinae: Dacini) of Bangladesh

Figure 23. Dacus (Callantra) longicornis Wiedemann. A) Head. B) Head and scutum. C) Abdomen, male. D) Wing. E) Distribution in Bangladesh. F) Lateral view, female. G) Lateral view, male.

opencc-by-4.0Aug 2021View details →
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Figure 19 in New country records, annotated checklist and key to the dacine fruit flies (Diptera: Tephritidae: Dacinae: Dacini) of Bangladesh

Figure 19. Bactrocera (Bactrocera) tuberculata (Bezzi). A) Head. B) Head and scutum. C) Abdomen, female. D) Abdomen, male. E) Wing (after Leblanc et al. 2014). F) Distribution in Bangladesh. G) Lateral view, female. H) Lateral view, male.

opencc-by-4.0Aug 2021View details →
zenodo28/100

Figs. 22–27 in Biology And Description Of The Third Instar Larva And Puparium Of Ichneumonopsis Burmensis Hardy (Diptera: Tephritidae: Dacinae: Gastrozonini), A Bamboo-Breeding Fruit Fly From The Oriental Region

Figs. 22–27. Pseudocephalon of I. burmensis larva showing the sense organs (SEM pictures). 22, Pseudocephalon and prothorax. 23, Antenna and maxillary sense organ. 24, Maxillary sense organ. 25, Stomal organ. 26, Detail of pseudocephalon showing the labial lobe, labial organ and pad organ. 27, Apical part of the labial lobe and the labial organ. ac pl = accessory plates; ant = antenna; lal = labial lobe; la org = labial organ; mh = mouth hook; max org = maxillary sense organ; or lb = oral lobe; or rdg = oral ridges; pad org= pad organ; pas A = papilla sensillum A; pas B = papilla sensillum B; pegs = peg sensillum; pits = pit sensillum; sto org = stomal organ.

opencc-by-4.0Feb 2013View details →
zenodo28/100

Figs. 1–7 in Biology And Description Of The Third Instar Larva And Puparium Of Ichneumonopsis Burmensis Hardy (Diptera: Tephritidae: Dacinae: Gastrozonini), A Bamboo-Breeding Fruit Fly From The Oriental Region

Figs. 1–7. Adults, habitat and development of I. burmensis-larvae. 1, Habitus of I. burmensis female. 2, Bamboo stand of M. compactiflorus in north Thailand at the edge of a field in November. The bamboo shoot in the front was damaged by a larva of the weevil Cyrtotrachelus sp. and the apical part of the main stem has dropped to the ground (large arrow points to the stump of the main stem). One of the resulting side branches of the main stem is infested by an I. burmensis larva (ii). The large side branch on the left has taken over the function of the main stem. 3, Cross-section through an M. compactiflorus internode near the apex of the bamboo shoot (diameter: 7 mm). The internode cavity contains white pith. 4, Apical part of an infested bamboo shoot of M. compactiflorus. The arrow points to the internode containing an I. burmensis larva. The upper internodes are dead but still attached to the bamboo shoot. 5, I. burmensis larva feeding on the white pith inside a bamboo internode (diameter of the internode cavity: 3–4 mm). 6, Bamboo fibres, ca. 5–7 cm long, recently torn off by the larva. 7, Lateral cut through an I. burmensis-internode (base of the internode on the left). The larva has eaten up about half of the white pith in the basal part the internode cavity and has freshly pupated at the base of the internode. Note the thin bamboo wall at the level of the exit hole. Most of the torn off vascular fibres have been removed in order to show the puparium. They filled the cavity beween the puparium and the "vf" arrow. eh = exit hole; bp = bamboo pith; bb = branch bud; ii = I. burmensis-internode; p = puparium; vf = vascular fibres.

opencc-by-4.0Feb 2013View details →
zenodo28/100

Supplementary material 2 from: Leblanc L, Tsatsia F, Doorenweerd C (2021) Novel lures and COI sequences reveal cryptic new species of Bactrocera fruit flies in the Solomon Islands (Diptera, Tephritidae, Dacini). ZooKeys 1057: 49-103. https://doi.org/10.3897/zookeys.1057.68375

Table S1. Pairwise molecular distance

opencc-zeroSep 2021View details →
zenodo28/100

Figure 4 from: Leblanc L, Tsatsia F, Doorenweerd C (2021) Novel lures and COI sequences reveal cryptic new species of Bactrocera fruit flies in the Solomon Islands (Diptera, Tephritidae, Dacini). ZooKeys 1057: 49-103. https://doi.org/10.3897/zookeys.1057.68375

Figure 4 Bactrocera pseudodistincta (Drew) A head B head and scutum C abdomen D wing E lateral view.

opencc-by-4.0Sep 2021View details →
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Figure 6 from: Leblanc L, Tsatsia F, Doorenweerd C (2021) Novel lures and COI sequences reveal cryptic new species of Bactrocera fruit flies in the Solomon Islands (Diptera, Tephritidae, Dacini). ZooKeys 1057: 49-103. https://doi.org/10.3897/zookeys.1057.68375

Figure 6 Bactrocera geminosimulata sp. nov. A head B head and scutum C abdomen D lateral view and wing.

opencc-by-4.0Sep 2021View details →
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Figure 3 from: Leblanc L, Tsatsia F, Doorenweerd C (2021) Novel lures and COI sequences reveal cryptic new species of Bactrocera fruit flies in the Solomon Islands (Diptera, Tephritidae, Dacini). ZooKeys 1057: 49-103. https://doi.org/10.3897/zookeys.1057.68375

Figure 3 Bactrocera allodistincta sp. nov. A head B head and scutum C abdomen D male genitalia E wing F lateral view.

opencc-by-4.0Sep 2021View details →
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Figure 28 from: Leblanc L, Tsatsia F, Doorenweerd C (2021) Novel lures and COI sequences reveal cryptic new species of Bactrocera fruit flies in the Solomon Islands (Diptera, Tephritidae, Dacini). ZooKeys 1057: 49-103. https://doi.org/10.3897/zookeys.1057.68375

Figure 28 Bactrocera moluccensis (Perkins) A head and scutum B abdomen C wing. Bactrocera furvescens Drew D head and scutum E abdomen F wing. Bactrocera aterrima (Drew) G head and scutum H abdomen I wing. Bactrocera parafroggatti Drew &amp; Romig J head and scutum K abdomen L wing.

opencc-by-4.0Sep 2021View details →
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Figure 27 from: Leblanc L, Tsatsia F, Doorenweerd C (2021) Novel lures and COI sequences reveal cryptic new species of Bactrocera fruit flies in the Solomon Islands (Diptera, Tephritidae, Dacini). ZooKeys 1057: 49-103. https://doi.org/10.3897/zookeys.1057.68375

Figure 27 Bactrocera pacificae Drew &amp; Romig A head and scutum B abdomen C female wing D male wing. Bactrocera buinensis Drew E head and scutum F abdomen G wing. Bactrocera unipunctata (Malloch) (reproduced from Drew 1989) H head and scutum I abdomen J wing. Bactrocera aithogaster Drew K scutum L abdomen M wing.

opencc-by-4.0Sep 2021View details →
zenodo28/100

Supplementary material 1 from: Leblanc L, Tsatsia F, Doorenweerd C (2021) Novel lures and COI sequences reveal cryptic new species of Bactrocera fruit flies in the Solomon Islands (Diptera, Tephritidae, Dacini). ZooKeys 1057: 49-103. https://doi.org/10.3897/zookeys.1057.68375

Figure S1. COI Phylogeny

opencc-zeroSep 2021View details →

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Last verified 2026-04-30Open record

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International Brain Laboratory public data

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Last verified 2026-04-29Open record

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Last verified 2026-04-29Open record