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54 results for “Bradysia”
Fig. 7 in Taxonomy of Bradysia Winnertz (Diptera, Sciaridae) in the Northern Holarctic, with the description of four new species
Fig. 7. Bradysia quercina Menzel & Köhler, 2014 (from Sweden). A. Part of hypopygium, ventral view. B. Gonostylus, ventral view. C. Apical part of gonostylus, ventral view. Scales = 0.1 mm.
Fig. 6 in Taxonomy of Bradysia Winnertz (Diptera, Sciaridae) in the Northern Holarctic, with the description of four new species
Fig. 6. Bradysia plusiospina sp. nov. (holotype). A. Part of hypopygium, ventral view. B. Gonostylus, ventral view. Scales = 0.1 mm.
Fig. 5 in Taxonomy of Bradysia Winnertz (Diptera, Sciaridae) in the Northern Holarctic, with the description of four new species
Fig. 5. Bradysia oelandica sp. nov. (holotype). A. Gonostylus, ventral view. B. Part of hypopygium, ventral view. C. Medial parts of hypopygium, ventral view. Scale bars: A = 0.1 mm, B–C = 0.3 mm. 1 = lobe at dorsal mesial margin of gonocoxa, 2 = tegmen, 3 = gonocoxal apodeme, 4 = aedeagal apodeme.
Fig. 4 in Taxonomy of Bradysia Winnertz (Diptera, Sciaridae) in the Northern Holarctic, with the description of four new species
Fig. 4. Bradysia falciceps sp. nov. (holotype). A. Part of hypopygium, ventral view. B. Gonostylus, ventral view. Scales = 0.1 mm.
Fig. 2 in Taxonomy of Bradysia Winnertz (Diptera, Sciaridae) in the Northern Holarctic, with the description of four new species
Fig. 2. Bradysia bigeminata sp. nov. (holotype). A. Part of hypopygium, ventral view. B. Gonostylus, ventral view. Scales = 0.1 mm.
Fig. 3 in Taxonomy of Bradysia Winnertz (Diptera, Sciaridae) in the Northern Holarctic, with the description of four new species
Fig. 3. Bradysia chlorocornea Mohrig & Menzel, 1992 (from Finland). A. Gonostylus, ventral view. B. Part of hypopygium, ventral view. Scales = 0.1 mm.
Fig. 1. Bradysia ascenda Rudzinski, 1994 in Taxonomy of Bradysia Winnertz (Diptera, Sciaridae) in the Northern Holarctic, with the description of four new species
Fig. 1. Bradysia ascenda Rudzinski, 1994 (from Sweden). A. Part of hypopygium, ventral view. B. Gonostylus, ventral view. C. Tegmen and cerci, ventral view. D. Apical part of gonostylus, ventral view. Scales = 0.1 mm.
Figs 38–46 in New Records Of Bradysia Species (Diptera, Sciaridae) From Ukraine
Figs 38–46. Bradysia polonica, male: 38 — thorax, lateral view; 39 — hypopygium, ventral view; 40 — anterior apex of fore tibia (t 1) with tibial organ, lateral view; 41 — gonostyli, ventral view; 42 — base of hypopygium with basal lobe, ventral view; 43 — eye bridge, frontal view; 44 — fourth flagellomere, lateral view; 45 — wing, dorsal view; 46 — maxillary palp, lateral view.
Figs 28–37 in New Records Of Bradysia Species (Diptera, Sciaridae) From Ukraine
Figs 28–37. Bradysia angustoocularis, imagoes: 28 — habitus of male, lateral view (terminalia removed, see fig. 34); 29 — habitus of female, lateral view; 30 — thorax, lateral view; 31 — fourth flagellomere, lateral view; 32 — maxillary palp, lateral view; 33 — anterior apex of fore tibia (t) with tibial organ, lateral view; 34 — 1 hypopygium, ventral view; 35 — gonostylus, ventral view; 36 — wing, dorsal view; 37 — eye bridge, frontal view. Scale bars: 28–29 — 1.0 mm; 30–37 — 0.10 mm.
Figs 18–27 in New Records Of Bradysia Species (Diptera, Sciaridae) From Ukraine
Figs 18–27. Bradysia cinerascens, male: 18 — thorax, lateral view; 19 — hypopygium, ventral view; 20 — base of hypopygium with basomedial group of bristles on inner membrane, ventral view; 21 — gonostylus, ventral view; 22 — anterior apex of fore tibia (t 1) with tibial organ, lateral view; 23 — basal palpomere of maxillary palp, lateral view; 24 — fourth flagellomere, lateral view; 25 — wing, dorsal view; 26 — eye bridge, frontal view; 27 — medial macrotrichia on y of specimen no. 207 (black arrow shows). Scale bars: 0.10 mm.
Figs 1–8 in New Records Of Bradysia Species (Diptera, Sciaridae) From Ukraine
Figs 1–8. Bradysia brevispina, male: 1 — thorax, lateral view; 2 — hypopygium, ventral view; 3 — anterior apex of fore tibia (t 1) with tibial organ, lateral view; 4 — gonostylus, ventral view; 5 — maxillary palp, lateral view; 6 — fourth flagellomere, lateral view; 7 — wing; 8 — eye bridge, frontal view. Scale bars: 0.10 mm.
Figs 9–17 in New Records Of Bradysia Species (Diptera, Sciaridae) From Ukraine
Figs 9–17. Bradysia microspina, male: 9 — thorax, lateral view; 10 — hypopygium, ventral view; 11 —anterior apex of fore tibia (t 1) with tibial organ, lateral view; 12 — gonostylus, ventral view; 13 — maxillary palp, lateral view; 14 — eye bridge, frontal view; 15 — 1 distal macrotrichia on y (black arrow shows); 16 — wing, dorsal view; 17 — fourth flagellomere, lateral view. Scale bars: 0.10 mm.
Linked collectors and determiners for: Definition of the Bradysia luctifica group (Diptera, Sciaridae), with the description of five new species.
Natural history specimen data linked to collectors and determiners held within, "Definition of the Bradysia luctifica group (Diptera, Sciaridae), with the description of five new species". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/f1c5d605-7034-4f05-bea5-f9b28f5de6e7">https://bionomia.net/dataset/f1c5d605-7034-4f05-bea5-f9b28f5de6e7</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/f1c5d605-7034-4f05-bea5-f9b28f5de6e7">https://gbif.org/dataset/f1c5d605-7034-4f05-bea5-f9b28f5de6e7</a>. Formatted as a Frictionless Data package.
Fitness of two mushroom flies Bradysia minpleuroti (Diptera: Sciaridae) and Coboldia fuscipes (Diptera: Scatopsidae) fed on two edible mushrooms
<p><a name="OLE_LINK220"></a><a name="OLE_LINK189"></a><em>Dictyophora</em> <em>rubrovolvata</em> and <a name="OLE_LINK87"></a><em>Pleurotus</em> <em>ostreatus</em> are economically important mushrooms in China. <a name="_Hlk146231531"></a><em>Bradysia</em> <em>minpleuroti</em> Yang et Zhang and <a name="OLE_LINK71"></a><em>Cobolidia</em> <em>fuscipes</em> (Meigen, 1830) are important mushroom flies that damage the two mushrooms. In this study we used the age-stage, two-sex life table method assessed <a name="_Hlk146230932"></a>the fitness of <a name="_Hlk143696432"></a><em>B</em>. <em>minpleuroti</em> and <em>C</em>. <em>fuscipes</em> when they were respectively fed on <a name="OLE_LINK20"></a><em>D</em>. <em>rubrovolvata</em> and <em>P</em>. <em>ostreatus</em>. Our results showed that the 1st (2.39 days) and 2nd (1.41 days) instar larvae, pupa (2.87 days) and total longevity (18.19 days) of <em>B</em>. <em>minpleuroti</em> were shorter when fed on <em>P</em>. <em>ostreatus</em> than fed on <em>D</em>. <em>rubrovolvata </em>(3.46, 1.86, 3.10, 20.19 days). <a name="OLE_LINK233"></a><em>B</em>. <em>minpleuroti</em> had similar fecundity when fed on the two edible mushrooms. <em>B</em>. <em>minpleuroti</em> had higher values of net reproductive rate (<em>R</em><sub>0</sub>, 87.73), intrinsic rate of increase (<em>r</em>, 0.2604), and finite rate of increase (<em>λ</em>, 1.2974) and shorter mean generation time (<em>T</em>, 17.19) when fed on <em>P</em>. <em>ostreatus</em> than fed on <em>D</em>. <em>rubrovalvata</em>. The developmental period of larvae stage and pupa stage of <em>C</em>. <em>fuscipes</em> were significantly affected by the two edible mushrooms. Female fecundity, total longevity, <em>R</em><sub>0</sub>, <em>r</em>, <em>λ</em> and <em>T</em> of <em>C</em>. <em>fuscipes</em> were not significantly different between the two edible mushrooms. We found that<a name="OLE_LINK174"></a> fitness of <em>B</em>. <em>minpleuroti</em> larvae had higher fitness when fed on <em>P</em>. <em>ostreatus</em> than fed on <em>D</em>. <em>rubrovolvata</em>. However, <a name="OLE_LINK183"></a>the fitness of <em>C</em>. <em>fuscipes</em> larvae had no significant difference fed on the two edible mushrooms. This study has provided valuable data and insights by delving into the adaptability of two significant pests on two edible mushrooms. It facilitates the development of more effective pest management strategies, contributing to the development of the mushroom industry.</p>
Effects of the entomopathogenic fungus Mucor hiemalis BO-1 on the physical functions and transcriptional signatures of Bradysia odoriphaga larvae
<p><em><span>Mucor hiemalis</span></em><span> BO-1 is an entomopathogenic fungus that infects <em>Bradysia</em> <em>odoriphaga</em>, a destructive root maggot. <em>M</em>. <em>hiemalis</em> BO-1 possesses stronger pathogenicity to the larvae than to other stages of <em>B</em>. <em>odoriphaga</em> and provides satisfactory field control. However, the physiological response of <em>B</em>. <em>odoriphaga</em> larvae to infection and the infection mechanism of <em>M</em>. <em>hiemalis</em> are unknown. We detected some physiological indicators of diseased <em>B</em>. <em>odoriphaga</em> larvae infected by <em>M</em>. <em>hiemalis</em> BO-1. These included changes in consumption, nutrient contents and digestive and antioxidant enzymes. We performed transcriptome analysis of diseased <em>B</em>. <em>odoriphaga</em> larvae and found that M. <em>hiemalis</em> BO-1 showed acute toxicity to <em>B</em>. <em>odoriphaga</em> larvae and was as toxic as some chemical pesticides. The food consumption of diseased <em>B</em>. <em>odoriphaga</em> after inoculation with <em>M</em>. <em>hiemalis</em> spores decreased significantly, and there was a significant decrease in total protein, lipid and carbohydrates in diseased larvae. Key digestive enzymes (protease, </span>α<span>-amylase, lipase and cellulase) were significantly inhibited during infection. Peroxidase maintained high activity, and the activity of other antioxidant enzymes (catalase, superoxide dismutase and glutathione S-transferases) first increased and then decreased. Combined with the transcriptional signatures of diseased <em>B</em>. <em>odoriphaga</em> larvae, <em>M</em>. <em>hiemalis</em> BO-1 infection resulted in decreased food consumption, reduced digestive enzyme activity and altered energy metabolism and material accumulation. Infection was also accompanied by fluctuations in immune function, such as cytochrome P450 and the Toll pathway. Therefore, our results laid a basis for the further study of the interactions between <em>M</em>. <em>hiemalis</em> BO-1 and <em>B</em>. <em>odoriphaga</em> and promoted the genetic improvement of entomopathogenic fungi.</span></p>
Effects of the entomopathogenic fungus Mucor hiemalis BO-1 on the physical functions and transcriptional signatures of Bradysia odoriphaga larvae
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FIGURE 3 A–D. Bradysia boninensis Steffan, 1969. Holotype. A in Revision of the black fungus gnat species (Diptera: Sciaridae) described by W.A. Steffan from Micronesia
FIGURE 3 A–D. Bradysia boninensis Steffan, 1969. Holotype. A. Hypopygium; B. Flagellomeres 1–5; C. Palpus; D. Wing.
FIGURE 4 A–C. Bradysia kraussi Steffan, 1969. Holotype. A in Revision of the black fungus gnat species (Diptera: Sciaridae) described by W.A. Steffan from Micronesia
FIGURE 4 A–C. Bradysia kraussi Steffan, 1969. Holotype. A. Hypopygium; B. Head with palpus and basal segments of flagellomeres; C. Gonostylus from Bradysia snyderi Steffan, 1969, syn. n. of B. kraussi.
Data sets of preference for Mucor circinelloides over edible mushrooms in the fungus gnat Bradysia impatiens
<p>This is the raw data for the olfactory response experiments on preference for <em>Mucor circinelloides</em> over edible mushrooms in the fungus gnat <em>Bradysia impatiens</em> (Diptera: Sciaridae).</p>
FIGURE 13 in The genus Bradysia Winnertz (Diptera, Sciaridae) in New Caledonia, with the description of thirteen new species
FIGURE 13. Bradysia stricta sp. n. (A paratype, B–D holotype). A. Antennal flagellomere 4, lateral view. B. Apical part of front tibia, prolateral view. C. Part of hypopygium, ventral view. D. Gonostylus, ventral view. Scale 0.1 mm.
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