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Data from: Molecular phylogeny of the horse flies: a framework for renewing tabanid taxonomy
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Figure 5 from: Sabbatini Peverieri G, Mitroiu M-D, Bon M-C, Balusu R, Benvenuto L, Bernardinelli I, Fadamiro H, Falagiarda M, Fusu L, Grove E, Haye T, Hoelmer K, Lemke E, Malossini G, Marianelli L, Moore MR, Pozzebon A, Roversi P-F, Scaccini D, Shrewsbury P, Tillman G, Tirello P, Waterworth R, Talamas EJ (2019) Surveys of stink bug egg parasitism in Asia, Europe and North America, morphological taxonomy, and molecular analysis reveal the Holarctic distribution of Acroclisoides sinicus (Huang & Liao) (Hymenoptera, Pteromalidae). Journal of Hymenoptera Research 74: 123-151. https://doi.org/10.3897/jhr.74.46701
Figure 5 Boxplot of pair-wise molecular distances between (left) the Acroclisoides haplotypes evidenced in this study, (center) conspecific individuals in the Pteromalinae, (right) individuals from different species of the same genus in the Pteromalinae.
Figure 4 from: Sabbatini Peverieri G, Mitroiu M-D, Bon M-C, Balusu R, Benvenuto L, Bernardinelli I, Fadamiro H, Falagiarda M, Fusu L, Grove E, Haye T, Hoelmer K, Lemke E, Malossini G, Marianelli L, Moore MR, Pozzebon A, Roversi P-F, Scaccini D, Shrewsbury P, Tillman G, Tirello P, Waterworth R, Talamas EJ (2019) Surveys of stink bug egg parasitism in Asia, Europe and North America, morphological taxonomy, and molecular analysis reveal the Holarctic distribution of Acroclisoides sinicus (Huang & Liao) (Hymenoptera, Pteromalidae). Journal of Hymenoptera Research 74: 123-151. https://doi.org/10.3897/jhr.74.46701
Figure 4 Haplotype network of the 49 Acroclisoides sinicus barcodes analyzed in this study. Each circle corresponds to one haplotype; circle size gives the proportion of individuals belonging to the haplotype. The color of the circles represents the geographical origin. Numbers correspond to the haplotype numbers. Hash marks symbolize the number of mutations between haplotypes.
Figure 1 from: Sabbatini Peverieri G, Mitroiu M-D, Bon M-C, Balusu R, Benvenuto L, Bernardinelli I, Fadamiro H, Falagiarda M, Fusu L, Grove E, Haye T, Hoelmer K, Lemke E, Malossini G, Marianelli L, Moore MR, Pozzebon A, Roversi P-F, Scaccini D, Shrewsbury P, Tillman G, Tirello P, Waterworth R, Talamas EJ (2019) Surveys of stink bug egg parasitism in Asia, Europe and North America, morphological taxonomy, and molecular analysis reveal the Holarctic distribution of Acroclisoides sinicus (Huang & Liao) (Hymenoptera, Pteromalidae). Journal of Hymenoptera Research 74: 123-151. https://doi.org/10.3897/jhr.74.46701
Figure 1 Typical shapes of exit holes produced by egg parasitoids of Halyomorpha halys in Europe: Anastatus bifasciatus male (A) and female (B) (NE-Italy); Acroclisoides sinicus (C, D) (NE-Italy); Trissolcus mitsukurii (E) (NE-Italy) and Trissolcus japonicus (F) (Switzerland).
Figure 3 from: Sabbatini Peverieri G, Mitroiu M-D, Bon M-C, Balusu R, Benvenuto L, Bernardinelli I, Fadamiro H, Falagiarda M, Fusu L, Grove E, Haye T, Hoelmer K, Lemke E, Malossini G, Marianelli L, Moore MR, Pozzebon A, Roversi P-F, Scaccini D, Shrewsbury P, Tillman G, Tirello P, Waterworth R, Talamas EJ (2019) Surveys of stink bug egg parasitism in Asia, Europe and North America, morphological taxonomy, and molecular analysis reveal the Holarctic distribution of Acroclisoides sinicus (Huang & Liao) (Hymenoptera, Pteromalidae). Journal of Hymenoptera Research 74: 123-151. https://doi.org/10.3897/jhr.74.46701
Figure 3 Acroclisoides sinicus: paratype of A. solus ♀ (U.S.A.), habitus in lateral view (A); idem, head in frontal view (B); ♂ (Switzerland), habitus in lateral view (C); idem, head in frontal view (D).
Figure 2 from: Sabbatini Peverieri G, Mitroiu M-D, Bon M-C, Balusu R, Benvenuto L, Bernardinelli I, Fadamiro H, Falagiarda M, Fusu L, Grove E, Haye T, Hoelmer K, Lemke E, Malossini G, Marianelli L, Moore MR, Pozzebon A, Roversi P-F, Scaccini D, Shrewsbury P, Tillman G, Tirello P, Waterworth R, Talamas EJ (2019) Surveys of stink bug egg parasitism in Asia, Europe and North America, morphological taxonomy, and molecular analysis reveal the Holarctic distribution of Acroclisoides sinicus (Huang & Liao) (Hymenoptera, Pteromalidae). Journal of Hymenoptera Research 74: 123-151. https://doi.org/10.3897/jhr.74.46701
Figure 2 Acroclisoides sinicus, ♀ (Italy, Cordenons): habitus in dorso-lateral view (A); head in frontal view (B); head in dorsal view (C); fore wing (D); antennae (E); mesosoma in dorsal view (F); mesosoma in lateral view (G).
Supplementary material 2 from: Nazari V, ten Hagen W (2020) Molecular taxonomy of Tomares hairstreaks (Lepidoptera, Lycaenidae, Theclinae). Deutsche Entomologische Zeitschrift 67(1): 19-33. https://doi.org/10.3897/dez.67.50252
SI 2. Male and female genitalia dissections of Tomares species.
Figure 2 from: Nazari V, ten Hagen W (2020) Molecular taxonomy of Tomares hairstreaks (Lepidoptera, Lycaenidae, Theclinae). Deutsche Entomologische Zeitschrift 67(1): 19-33. https://doi.org/10.3897/dez.67.50252
Figure 2 Neighbour-Joining tree of 271 barcode sequences of Tomares. Values are bootstrap of 100 replicates for supported nodes.
Figure 1 from: Nazari V, ten Hagen W (2020) Molecular taxonomy of Tomares hairstreaks (Lepidoptera, Lycaenidae, Theclinae). Deutsche Entomologische Zeitschrift 67(1): 19-33. https://doi.org/10.3897/dez.67.50252
Figure 1 Right valvae in male genitalia of Tomares species. 1.T. mauritanicus GP76 (Morocco); 2.T. ballus GP77 (Morocco); 3.T. fedtschenkoi GP78 (Tajikstan); 4.T. desinens GP86 (Qazvin, Iran); 5.T. callimachus callimachus GP75 (Crimea); 6.T. callimachus hafis GP86 (Zanjan, Iran); 7.T. nesimachus GP84 (Damascus, Syria); 8.T. "telemachus" GP79 (Turkmenistan); 9.T. romanovi GP74 (Lorestan, Iran); 10.T. nogelii nogelii GP88 (Nevshehir, Turkey); 11.T. nogelii nogelii GP85 (Sivas, Turkey); 12.T. nogelii dobrogensis GP83 (Ukraine). All dissections and images by WtH.
Figure 4 from: Nazari V, ten Hagen W (2020) Molecular taxonomy of Tomares hairstreaks (Lepidoptera, Lycaenidae, Theclinae). Deutsche Entomologische Zeitschrift 67(1): 19-33. https://doi.org/10.3897/dez.67.50252
Figure 4 Distribution of taxa in the nogelii complex. Shapes represent morphological identifications (□ = nogelii, ∆ = nesimachus, ○ = romanovi), colors represent COI barcode haplotypes (red = nogelii haplotypes, orange = nesimachus haplotypes, green = romanovi haplotypes). Sites with shared or more than one haplotypes are circled. Records in gray are concatenated from literature. Approximate taxon boundaries are inferred from represented haplotypes. For haplotype network, see Figure 3.
Figure 3 from: Nazari V, ten Hagen W (2020) Molecular taxonomy of Tomares hairstreaks (Lepidoptera, Lycaenidae, Theclinae). Deutsche Entomologische Zeitschrift 67(1): 19-33. https://doi.org/10.3897/dez.67.50252
Figure 3 TCS Haplotype Network of the nogelii complex. Colors indicate morphological identifications (red = nogelii, blue = dobrogensis, orange = nesimachus, green = romanovi, yellow = telemachus). The most common haplotype (large circle) comprises central and eastern Turkish individuals of nogelii, 'nesimachus' and 'dobrogensis', as well as a single nesimachus from Israel.
Figure 5 from: Nazari V, ten Hagen W (2020) Molecular taxonomy of Tomares hairstreaks (Lepidoptera, Lycaenidae, Theclinae). Deutsche Entomologische Zeitschrift 67(1): 19-33. https://doi.org/10.3897/dez.67.50252
Figure 5 Bayesian phylogeny of selected Tomares sequences based on combined data (COI + EF-1α). Values above branches are bootstrap support obtained under Parsimony and Likelihood criteria for each node, and values below branches are Bayesian posterior probabilities. Images: 1) ballus wth013 Morocco, 2) ballus wth055 Spain, 3) mauritanicus wth017 Morocco, 4) fedtchenkoi wth020 Kyrgyzstan, 5) callimachuscallimachus wth051 Azerbaijan, 6) callimachushafis wth053 Iran, 7) desinens wth042 Iran, 8) dobrogensis wth080 Crimea, 9) nogelii zma153 Turkey, 10) nesimachus wth065 Syria, 11) romanoviobscura zma161 Turkey, 12) romanovicachetinus zma146 Azerbaijan, 13) romanoviromanovi wth010 Armenia, 14) telemachus wth005 Turkmenistan.
Supplementary material 1 from: Nazari V, ten Hagen W (2020) Molecular taxonomy of Tomares hairstreaks (Lepidoptera, Lycaenidae, Theclinae). Deutsche Entomologische Zeitschrift 67(1): 19-33. https://doi.org/10.3897/dez.67.50252
SI 1. Material examined and Genbank accessions.
Supplementary material 3 from: Nazari V, ten Hagen W (2020) Molecular taxonomy of Tomares hairstreaks (Lepidoptera, Lycaenidae, Theclinae). Deutsche Entomologische Zeitschrift 67(1): 19-33. https://doi.org/10.3897/dez.67.50252
SI 3. Androconia, forewing upperside and hindwing underside in select Tomares species.
Supplementary material 2 from: Wang P, Che J, Liu Q, Li K, Jin JQ, Jiang K, Shi L, Guo P (2020) A revised taxonomy of Asian snail-eating snakes Pareas (Squamata, Pareidae): evidence from morphological comparison and molecular phylogeny. ZooKeys 939: 45-64. https://doi.org/10.3897/zookeys.939.49309
Appendix S2
Supplementary material 1 from: Wang P, Che J, Liu Q, Li K, Jin JQ, Jiang K, Shi L, Guo P (2020) A revised taxonomy of Asian snail-eating snakes Pareas (Squamata, Pareidae): evidence from morphological comparison and molecular phylogeny. ZooKeys 939: 45-64. https://doi.org/10.3897/zookeys.939.49309
Appendix S1
Supplementary material 4 from: Wang P, Che J, Liu Q, Li K, Jin JQ, Jiang K, Shi L, Guo P (2020) A revised taxonomy of Asian snail-eating snakes Pareas (Squamata, Pareidae): evidence from morphological comparison and molecular phylogeny. ZooKeys 939: 45-64. https://doi.org/10.3897/zookeys.939.49309
Figure 1
Figure 3 from: Wang P, Che J, Liu Q, Li K, Jin JQ, Jiang K, Shi L, Guo P (2020) A revised taxonomy of Asian snail-eating snakes Pareas (Squamata, Pareidae): evidence from morphological comparison and molecular phylogeny. ZooKeys 939: 45-64. https://doi.org/10.3897/zookeys.939.49309
Figure 3 The comparisons of dorsal head (row 1) and median dorsal (row 2) between Pareas macularius and P. margaritophorus. AP. margaritophorusBP. macularius.
Figure 2 from: Wang P, Che J, Liu Q, Li K, Jin JQ, Jiang K, Shi L, Guo P (2020) A revised taxonomy of Asian snail-eating snakes Pareas (Squamata, Pareidae): evidence from morphological comparison and molecular phylogeny. ZooKeys 939: 45-64. https://doi.org/10.3897/zookeys.939.49309
Figure 2 Bayesian inference(left) and Maximum Likelihood(right) trees of the Pareidae based on mtDNA dataset. Branch support measures are Bayesian posterior probabilities and ML bootstrap support respectively. Branch support indices are not given for most intrageneric nodes to preserve clarity.
Supplementary material 3 from: Wang P, Che J, Liu Q, Li K, Jin JQ, Jiang K, Shi L, Guo P (2020) A revised taxonomy of Asian snail-eating snakes Pareas (Squamata, Pareidae): evidence from morphological comparison and molecular phylogeny. ZooKeys 939: 45-64. https://doi.org/10.3897/zookeys.939.49309
Appendix S3
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International Brain Laboratory public data
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OpenNeuro
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