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507 results for “symbionts”
Figures 43-49 from: Kanao T, Maruyama M (2012) Two new genera and species of the termite symbiont lineage Termitohospitini (Coleoptera, Staphylinidae, Aleocharinae) from Bolivia and peninsular Malaysia. ZooKeys 254: 67-87. https://doi.org/10.3897/zookeys.254.4043
Figures 43-49 - Coptotermocola clavicornis, abdominal sclerites and genitalia. 43 tergite VIII 44 sternite VIII 45 tergites IX–X 46 median lobe of aedeagus, aparameral view 47 median lobe of aedeagus, lateral view 48 paramere, external view 49 spermatheca.
Figures 11-16 from: Kanao T, Maruyama M (2012) Two new genera and species of the termite symbiont lineage Termitohospitini (Coleoptera, Staphylinidae, Aleocharinae) from Bolivia and peninsular Malaysia. ZooKeys 254: 67-87. https://doi.org/10.3897/zookeys.254.4043
Figures 11-16 - Neotermitosocius bolivianus, thorax and legs. 11 pronotum, left side with setae 12 elytron, left 13 meso- and metaventrites, anatomical left side with setae 14 fore leg, posterior surface 15 mid leg, anterior surface 16 hind leg, anterior surface.
Figure 28-29 from: Kanao T, Maruyama M (2012) Two new genera and species of the termite symbiont lineage Termitohospitini (Coleoptera, Staphylinidae, Aleocharinae) from Bolivia and peninsular Malaysia. ZooKeys 254: 67-87. https://doi.org/10.3897/zookeys.254.4043
Figure 28-29 - Coptotermocola clavicornis. 28 head capsule left side = dorsal view, right side = ventral view 29 antenna.
Figures 24-27 from: Kanao T, Maruyama M (2012) Two new genera and species of the termite symbiont lineage Termitohospitini (Coleoptera, Staphylinidae, Aleocharinae) from Bolivia and peninsular Malaysia. ZooKeys 254: 67-87. https://doi.org/10.3897/zookeys.254.4043
Figures 24-27 - Habitus of Coptotermocola clavicornis. 24 beetle photographed in situ 25 dorsal view 26 lateral view 27 ventral view.
Figures 5-10 from: Kanao T, Maruyama M (2012) Two new genera and species of the termite symbiont lineage Termitohospitini (Coleoptera, Staphylinidae, Aleocharinae) from Bolivia and peninsular Malaysia. ZooKeys 254: 67-87. https://doi.org/10.3897/zookeys.254.4043
Figures 5-10 - Neotermitosocius bolivianus mouthparts. 5 labrum, left side = labrum, right side = epipharynx 6 left mandible, dorsal view 7 right mandible, dorsal view 8 maxilla, ventral view 9 mentum, ventral view 10 labium in ventral view.
Figures 36-42 from: Kanao T, Maruyama M (2012) Two new genera and species of the termite symbiont lineage Termitohospitini (Coleoptera, Staphylinidae, Aleocharinae) from Bolivia and peninsular Malaysia. ZooKeys 254: 67-87. https://doi.org/10.3897/zookeys.254.4043
Figures 36-42 - Coptotermocola clavicornis, thorax and legs. 36 pronotum, left side with and right side without setae 37 elytron, left 38 meso- and metaventrites, anatomical left side with setae 39 detail of mesosternal process surface sculpture 40 fore leg, posterior surface 41 mid leg, posterior surface 42 hind leg, posterior surface.
Figures 3-4 from: Kanao T, Maruyama M (2012) Two new genera and species of the termite symbiont lineage Termitohospitini (Coleoptera, Staphylinidae, Aleocharinae) from Bolivia and peninsular Malaysia. ZooKeys 254: 67-87. https://doi.org/10.3897/zookeys.254.4043
Figures 3-4 - Neotermitosocius bolivianus. 3 head capsule, left side = dorsal view, right side = ventral view 4 antenna.
Figure 2 from: Bochkov A, Abramov A (2014) Acariform mites (Acariformes) - permanent symbionts of Hapalomys delacouri Thomas (Rodentia, Muridae) in Vietnam. ZooKeys 459: 137-145. https://doi.org/10.3897/zookeys.459.8952
Figure 2 - Afrolistrophorus hapalomys sp. n., female, A lateral view B opisthosoma in dorsal view C ovipore D tibia and tarsus III in ventral view. Scale bars: A and B = 100 μm; C and D = 50 μm.
Figure 1 from: Bochkov A, Abramov A (2014) Acariform mites (Acariformes) - permanent symbionts of Hapalomys delacouri Thomas (Rodentia, Muridae) in Vietnam. ZooKeys 459: 137-145. https://doi.org/10.3897/zookeys.459.8952
Figure 1 - Afrolistrophorus hapalomys sp. n., male holotype, A dorsal view B ventral view C tarsus III in ventral view D tarsus IV ventral view. Scale bars: A and B = 50 μm; C and D = 25 μm.
Figure 3 from: Bochkov A, Abramov A (2014) Acariform mites (Acariformes) - permanent symbionts of Hapalomys delacouri Thomas (Rodentia, Muridae) in Vietnam. ZooKeys 459: 137-145. https://doi.org/10.3897/zookeys.459.8952
Figure 3 - Radfordia mirabilis sp. n., female holotype, A dorsal view B ventral view C vulva. Scale bars: A and B = 100 μm; C = 50 μm.
Figure 4 from: Augustinos AA, Drosopoulou E, Gariou-Papalexiou A, Asimakis ED, Cáceres C, Tsiamis G, Bourtzis K, Mavragani-Tsipidou P, Zacharopoulou A (2015) Cytogenetic and symbiont analysis of five members of the B. dorsalis complex (Diptera, Tephritidae): no evidence of chromosomal or symbiont-based speciation events. In: De Meyer M, Clarke AR, Vera MT, Hendrichs J (Eds) Resolution of Cryptic Species Complexes of Tephritid Pests to Enhance SIT Application and Facilitate International Trade. ZooKeys 540: 273-298. https://doi.org/10.3897/zookeys.540.9857
Figure 4 - Comparison of the 3L polytene chromosome arm of a Bactrocera tryoni and b Bactrocera dorsalis s.s.. Dot lines connect characteristic landmarks of the two chromosomes.
Figure 1 from: Augustinos AA, Drosopoulou E, Gariou-Papalexiou A, Asimakis ED, Cáceres C, Tsiamis G, Bourtzis K, Mavragani-Tsipidou P, Zacharopoulou A (2015) Cytogenetic and symbiont analysis of five members of the B. dorsalis complex (Diptera, Tephritidae): no evidence of chromosomal or symbiont-based speciation events. In: De Meyer M, Clarke AR, Vera MT, Hendrichs J (Eds) Resolution of Cryptic Species Complexes of Tephritid Pests to Enhance SIT Application and Facilitate International Trade. ZooKeys 540: 273-298. https://doi.org/10.3897/zookeys.540.9857
Figure 1 - a, b Polytene nuclei of Bactrocera dorsalis s.s. from China. Chromosome arms are shown. Tips are marked with arrows and centromeres are indicated with 'C'.
Figure 5 from: Augustinos AA, Drosopoulou E, Gariou-Papalexiou A, Asimakis ED, Cáceres C, Tsiamis G, Bourtzis K, Mavragani-Tsipidou P, Zacharopoulou A (2015) Cytogenetic and symbiont analysis of five members of the B. dorsalis complex (Diptera, Tephritidae): no evidence of chromosomal or symbiont-based speciation events. In: De Meyer M, Clarke AR, Vera MT, Hendrichs J (Eds) Resolution of Cryptic Species Complexes of Tephritid Pests to Enhance SIT Application and Facilitate International Trade. ZooKeys 540: 273-298. https://doi.org/10.3897/zookeys.540.9857
Figure 5 - Comparison of the 4L polytene chromosome arms of a Bactrocera tryoni and b Bactrocera dorsalis s.s.. Dot lines connect characteristic landmarks of the two chromosomes.
Figure 3 from: Augustinos AA, Drosopoulou E, Gariou-Papalexiou A, Asimakis ED, Cáceres C, Tsiamis G, Bourtzis K, Mavragani-Tsipidou P, Zacharopoulou A (2015) Cytogenetic and symbiont analysis of five members of the B. dorsalis complex (Diptera, Tephritidae): no evidence of chromosomal or symbiont-based speciation events. In: De Meyer M, Clarke AR, Vera MT, Hendrichs J (Eds) Resolution of Cryptic Species Complexes of Tephritid Pests to Enhance SIT Application and Facilitate International Trade. ZooKeys 540: 273-298. https://doi.org/10.3897/zookeys.540.9857
Figure 3 - Characteristic asynapsis in the 3L, close to the tip region, observed in Bactrocera dorsalis colony derived from China. a almost completely synapsed region b–d asynapses of the same region; asterisks (*) indicate the specific region.
Figure 2 from: Augustinos AA, Drosopoulou E, Gariou-Papalexiou A, Asimakis ED, Cáceres C, Tsiamis G, Bourtzis K, Mavragani-Tsipidou P, Zacharopoulou A (2015) Cytogenetic and symbiont analysis of five members of the B. dorsalis complex (Diptera, Tephritidae): no evidence of chromosomal or symbiont-based speciation events. In: De Meyer M, Clarke AR, Vera MT, Hendrichs J (Eds) Resolution of Cryptic Species Complexes of Tephritid Pests to Enhance SIT Application and Facilitate International Trade. ZooKeys 540: 273-298. https://doi.org/10.3897/zookeys.540.9857
Figure 2 - a–e Characteristic asynapsis in 5R chromosome arm, close to the centromere (regions 73–74), observed in the Bactrocera dorsalis s.s. colony derived from China. Asterisks (*) mark the asynaptic region, while 'C' marks the 5R centromere.
Figure 8 from: Augustinos AA, Drosopoulou E, Gariou-Papalexiou A, Asimakis ED, Cáceres C, Tsiamis G, Bourtzis K, Mavragani-Tsipidou P, Zacharopoulou A (2015) Cytogenetic and symbiont analysis of five members of the B. dorsalis complex (Diptera, Tephritidae): no evidence of chromosomal or symbiont-based speciation events. In: De Meyer M, Clarke AR, Vera MT, Hendrichs J (Eds) Resolution of Cryptic Species Complexes of Tephritid Pests to Enhance SIT Application and Facilitate International Trade. ZooKeys 540: 273-298. https://doi.org/10.3897/zookeys.540.9857
Figure 8 - a, b Polytene nuclei derived from the F1 Bactrocera dorsalis s.s. × Bactrocera tryoni hybrids. Chromosome arms are indicated. Tips are marked with arrows and centromeres are indicated with 'C'. Note the overall banding pattern homosequentiallity and the presence of limited asynapses.
Figure 9 from: Augustinos AA, Drosopoulou E, Gariou-Papalexiou A, Asimakis ED, Cáceres C, Tsiamis G, Bourtzis K, Mavragani-Tsipidou P, Zacharopoulou A (2015) Cytogenetic and symbiont analysis of five members of the B. dorsalis complex (Diptera, Tephritidae): no evidence of chromosomal or symbiont-based speciation events. In: De Meyer M, Clarke AR, Vera MT, Hendrichs J (Eds) Resolution of Cryptic Species Complexes of Tephritid Pests to Enhance SIT Application and Facilitate International Trade. ZooKeys 540: 273-298. https://doi.org/10.3897/zookeys.540.9857
Figure 9 - a–e Part of the 2R chromosome arm including the fixed inversion. Photos derived from different polytene chromosome preparations. Asterisks (*) indicate the inversion breakpoints. 'C' indicates the 2R centromere.
Figure 7 from: Augustinos AA, Drosopoulou E, Gariou-Papalexiou A, Asimakis ED, Cáceres C, Tsiamis G, Bourtzis K, Mavragani-Tsipidou P, Zacharopoulou A (2015) Cytogenetic and symbiont analysis of five members of the B. dorsalis complex (Diptera, Tephritidae): no evidence of chromosomal or symbiont-based speciation events. In: De Meyer M, Clarke AR, Vera MT, Hendrichs J (Eds) Resolution of Cryptic Species Complexes of Tephritid Pests to Enhance SIT Application and Facilitate International Trade. ZooKeys 540: 273-298. https://doi.org/10.3897/zookeys.540.9857
Figure 7 - The inverted region on the 2R polytene arm that differentiates Bactrocera tryoni from the five members of the Bactrocera dorsalis complex: a Bactrocera tryoni b Bactrocera dorsalis s.s. Dotted lines mark the chromosomal region involved in the inversion while arrows indicate the orientation.
Figure 6 from: Augustinos AA, Drosopoulou E, Gariou-Papalexiou A, Asimakis ED, Cáceres C, Tsiamis G, Bourtzis K, Mavragani-Tsipidou P, Zacharopoulou A (2015) Cytogenetic and symbiont analysis of five members of the B. dorsalis complex (Diptera, Tephritidae): no evidence of chromosomal or symbiont-based speciation events. In: De Meyer M, Clarke AR, Vera MT, Hendrichs J (Eds) Resolution of Cryptic Species Complexes of Tephritid Pests to Enhance SIT Application and Facilitate International Trade. ZooKeys 540: 273-298. https://doi.org/10.3897/zookeys.540.9857
Figure 6 - Comparison of the 5L polytene chromosome arms of a Bactrocera tryoni and b Bactrocera dorsalis s.s.. Dot lines connect characteristic landmarks of the two chromosomes.
Fig. 3 in Antibacterial harziane diterpenoids from a fungal symbiont Trichoderma atroviride isolated from Colquhounia coccinea var. mollis
Fig. 3. Key ROESY correlations of compounds 1–5.
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