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Figure 4 from: De Meyer M, Delatte H, Mwatawala M, Quilici S, Vayssières J-F, Virgilio M (2015) A review of the current knowledge on Zeugodacus cucurbitae (Coquillett) (Diptera, Tephritidae) in Africa, with a list of species included in Zeugodacus. 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: 539-557. https://doi.org/10.3897/zookeys.540.9672
Figure 4 - Individual admixture proportions (K=5) of 25 different populations of Zeugodacus cucurbitae (after Virgilio et al. 2010).
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: De Meyer M, Delatte H, Mwatawala M, Quilici S, Vayssières J-F, Virgilio M (2015) A review of the current knowledge on Zeugodacus cucurbitae (Coquillett) (Diptera, Tephritidae) in Africa, with a list of species included in Zeugodacus. 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: 539-557. https://doi.org/10.3897/zookeys.540.9672
Figure 3 - Distribution patterns for African tephritids: a Zeugodacus cucurbitae b Dacus ciliatus c Dacus bivittatus d Dacus vertebratus e Dacus frontalis f Dacus punctatifrons (source of data: http://projects.bebif.be/fruitfly/index.html).
Figure 2 from: Vaníčková L, Hernández-Ortiz V, Bravo ISJ, Dias V, Roriz AKP, Laumann RA, Mendonça AL, Paranhos BAJ, do Nascimento RR (2015) Current knowledge of the species complex Anastrepha fraterculus (Diptera, Tephritidae) in Brazil. 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: 211-237. https://doi.org/10.3897/zookeys.540.9791
Figure 2 - Scanning electron micrographs of the anterior tip (dorsal view) of eggs from Brazilian-1 (A), Brazilian-2 (B), Brazilian-3 (C) morphotype of Anastrepha fraterculus. The arrow shows aeropyles. Bars = 20 µm (A, B) and 50 µm (C). The images were modified from Selivon et al. 2004, and from Selivon and Perondini 1998, with permision.
Figure 2 from: De Meyer M, Delatte H, Mwatawala M, Quilici S, Vayssières J-F, Virgilio M (2015) A review of the current knowledge on Zeugodacus cucurbitae (Coquillett) (Diptera, Tephritidae) in Africa, with a list of species included in Zeugodacus. 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: 539-557. https://doi.org/10.3897/zookeys.540.9672
Figure 2 - NJ tree (K2P distance, Kimura 1980) including 44 COI DNA barcodes of Zeugodacus cucurbitae from 11 countries (Virgilio and De Meyer, unpublished data).
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 5 from: De Meyer M, Delatte H, Mwatawala M, Quilici S, Vayssières J-F, Virgilio M (2015) A review of the current knowledge on Zeugodacus cucurbitae (Coquillett) (Diptera, Tephritidae) in Africa, with a list of species included in Zeugodacus. 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: 539-557. https://doi.org/10.3897/zookeys.540.9672
Figure 5 - Zeugodacus cucurbitae specimens (n = 42) reared from four different hosts (Cucumis dipsaceus, Cucurbita sp., Luffa sp., Momordica rostrata) at the Sokoine University of Agriculture (Morogoro, Tanzania) and genotyped at 19 microsatellite loci (Mwatawala, Virgilio, De Meyer, unpublished data).
Figure 4 from: Vaníčková L, Hernández-Ortiz V, Bravo ISJ, Dias V, Roriz AKP, Laumann RA, Mendonça AL, Paranhos BAJ, do Nascimento RR (2015) Current knowledge of the species complex Anastrepha fraterculus (Diptera, Tephritidae) in Brazil. 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: 211-237. https://doi.org/10.3897/zookeys.540.9791
Figure 4 - The results of the multivariate principal component analysis (PCA) of the sex pheromone of the males of Anastrepha fraterculus from 7 different populations representing two Brazilian morphotypes (A. sp.1, A. sp.3). A. sp.1. PEL – Pelotas (RS, BR), BEN – Bento Gonçalves (RS, BR), VAC – Vacaria (RS, BR), SAO - São Joaquim (SC, BR), TUC – Tucumán (AR); A. sp.3. AL – Alagoas (AL, BR); PIRA – Piracicaba (SP, BR) [modified after Břízová et al. (2013)].
Figure 4 from: Vaníčková L, Břízová R, Pompeiano A, Ferreira LL, de Aquino NC, Tavares RF, Rodriguez LD, Mendonça AL, Canal NA, do Nascimento RR (2015) Characterisation of the chemical profiles of Brazilian and Andean morphotypes belonging to the Anastrepha fraterculus complex (Diptera, Tephritidae). 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: 193-209. https://doi.org/10.3897/zookeys.540.9649
Figure 4 - Principal component analyses (PCA) of transformed GC×GC/MS data of 48 female CHs from seven populations of the Anastrepha fraterculus cryptic species complex. (Variables factor map) projection of variables on the plane defined by the first two principal components. (Hierarchical clustering) score plot describing the populations and their clustering. Key: AL – Alagoas, AL, Brazil; BEN – Bento Gonçalves, RS, Brazil; CAC – Cachipay, Colombia; DUI – Duitama, Colombia; PEL – Pelotas, RS, Brazil; SAO – São Joaquim, SC, Brazil; SIB – Sibundoy, Colombia. A1–19 – n-alkanes; B1–11 – methylbranched hydrocarbons; C1–11 – alkenes; D1–7 – alkadienes. Colored boxes indicate particular clusters.
Figure 2 from: Van Cann J, Virgilio M, Jordaens K, De Meyer M (2015) Wing morphometrics as a possible tool for the diagnosis of the Ceratitis fasciventris, C. anonae, C. rosa complex (Diptera, Tephritidae). 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: 489-506. https://doi.org/10.3897/zookeys.540.9724
Figure 2 - Diagnostic performance at different identification thresholds. Proportions of male and female specimens consistently assigned (a) to morphospecies (i.e. of specimens for which the highest posterior group membership probabilities (PGMP) corresponds to the prior morphospecies grouping) and (b) to genotypic cluster (i.e. of specimens for which the highest PGMP corresponds to the prior A, F1, F2, R1, R2 genotypic grouping) when considering wing landmarks (left) or wing band areas (right) and by using different assignment thresholds (no threshold, PGMP = 0.95, PGMP = 0.99).
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 1 from: Vaníčková L, Hernández-Ortiz V, Bravo ISJ, Dias V, Roriz AKP, Laumann RA, Mendonça AL, Paranhos BAJ, do Nascimento RR (2015) Current knowledge of the species complex Anastrepha fraterculus (Diptera, Tephritidae) in Brazil. 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: 211-237. https://doi.org/10.3897/zookeys.540.9791
Figure 1 - Adult female Anastrepha fraterculus (A) and typical forms of the aculeus tip and the wing pattern of morphotypes Brazilian-1 (B, E), Brazilian-2 (C, F), Brazilian-3 (D, G), respectively. (The photo of adult was made by Dr. Hoskovec, the images of aculeus and wings were modified from Hernández-Ortiz et al. 2012).
Figure 2 from: Vaníčková L, Břízová R, Pompeiano A, Ferreira LL, de Aquino NC, Tavares RF, Rodriguez LD, Mendonça AL, Canal NA, do Nascimento RR (2015) Characterisation of the chemical profiles of Brazilian and Andean morphotypes belonging to the Anastrepha fraterculus complex (Diptera, Tephritidae). 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: 193-209. https://doi.org/10.3897/zookeys.540.9649
Figure 2 - Principal component analyses (PCA) of transformed GC×GC/MS data of seven male-borne volatiles produced by groups of 20 sexually mature individuals from seven populations of the Anastrepha fraterculus cryptic species complex. Variables factor map represents projection of variables on the plane defined by the first two principal components. Hierarchical clustering is score plot describing the populations and their clustering. Key: AL – Alagoas, AL, Brazil; BEN – Bento Gonçalves, RS, Brazil; DUI – Duitama, Colombia; IBA – Ibague, Colombia; PEL – Pelotas, RS, Brazil; SAO – São Joaquim, SC, Brazil; SIB – Sibundoy, Colombia. Epianas. – Epianastrephin; Z.E.Far – (Z, E)-α-farnesene; E.E.Far – (E, E)-α-farnesene; Nonen.1.ol – (Z)-3-nonen-1-ol; Nonadien. – (E, Z)-3,6-nonadien-1-ol; a.Pinene – α-pinene. Colored boxes indicate particular clusters.
Figure 3 from: Vaníčková L, Břízová R, Pompeiano A, Ferreira LL, de Aquino NC, Tavares RF, Rodriguez LD, Mendonça AL, Canal NA, do Nascimento RR (2015) Characterisation of the chemical profiles of Brazilian and Andean morphotypes belonging to the Anastrepha fraterculus complex (Diptera, Tephritidae). 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: 193-209. https://doi.org/10.3897/zookeys.540.9649
Figure 3 - Principal component analyses (PCA) of transformed GC×GC/MS data of 48 male CHs from seven populations of the Anastrepha fraterculus cryptic species complex. Variables factor map represents projection of variables on the plane defined by the first two principal components. Hierarchical clustering is score plot describing the populations and their clustering. Key: AL – Alagoas, AL, Brazil; BEN – Bento Gonçalves, RS, Brazil; CAC – Cachipay, Colombia; DUI – Duitama, Colombia; PEL – Pelotas, RS, Brazil; SAO – São Joaquim, SC, Brazil; SIB – Sibundoy, Colombia. A1–19 – n-alkanes; B1–11 – methylbranched hydrocarbons; C1–11 – alkenes; D1–7 – alkadienes. Colored boxes indicate particular clusters.
Figure 4 from: Břízová R, Vaníčková L, Faťarová M, Ekesi S, Hoskovec M, Kalinová B (2015) Analyses of volatiles produced by the African fruit fly species complex (Diptera, Tephritidae). 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: 385-404. https://doi.org/10.3897/zookeys.540.9630
Figure 4 - The results of statistical analyses of the male-borne volatiles produced by Ceratitis fasciventris (blue), Ceratitis anonae (green) and Ceratitis rosa (red). (A) Multivariate principal component analysis (PCA) of the 22 common compounds identified in the pheromone of the males of the FAR complex. (B) Multivariate correspondence analysis (CA) of the 12 antennal active compounds. The three species are clearly segregated. Each symbol on the plot represents one sample. The numbers in italics denote the retention indices (RI) of the species-specific compounds. For the structural identification of the compounds see the Suppl. materials 1–3: Tables 1–3.
Figure 1 from: Vaníčková L, Břízová R, Pompeiano A, Ferreira LL, de Aquino NC, Tavares RF, Rodriguez LD, Mendonça AL, Canal NA, do Nascimento RR (2015) Characterisation of the chemical profiles of Brazilian and Andean morphotypes belonging to the Anastrepha fraterculus complex (Diptera, Tephritidae). 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: 193-209. https://doi.org/10.3897/zookeys.540.9649
Figure 1 - Heat map of seven male-borne volatiles (columns) identified by GC×GC/MS analyses in seven populations (rows) of the Anastrepha fraterculus cryptic species complex. The dendrograms were created using correlation-based distances and the Ward method of hierarchical clustering (P < 0.05). Key: AL – Alagoas, AL, Brazil; BEN – Bento Gonçalves, RS, Brazil; DUI – Duitama, Colombia; IBA – Ibague, Colombia; PEL – Pelotas, RS, Brazil; SAO – São Joaquim, SC, Brazil; SIB – Sibundoy, Colombia. Epianas – Epianastrephin; Z.E.Far – (Z, E)-α-farnesene; E.E.Far – (E, E)-α-farnesene; Z.Nonenol – (Z)-3-nonen-1-ol; E.Z.Nona – (E, Z)-3,6-nonadien-1-ol; a.Pinene – α-pinene.
Figure 3 from: Břízová R, Vaníčková L, Faťarová M, Ekesi S, Hoskovec M, Kalinová B (2015) Analyses of volatiles produced by the African fruit fly species complex (Diptera, Tephritidae). 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: 385-404. https://doi.org/10.3897/zookeys.540.9630
Figure 3 - A comparison of female antennal responses of Ceratitis fasciventris, Ceratitis anonae, and Ceratitis rosa to standard solutions. The FID/EAD on the y-axis represents the ratio between an electroantennographic response and a conventional detector. The higher the number, the higher the response (N = 3).
Figure 2 from: Břízová R, Vaníčková L, Faťarová M, Ekesi S, Hoskovec M, Kalinová B (2015) Analyses of volatiles produced by the African fruit fly species complex (Diptera, Tephritidae). 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: 385-404. https://doi.org/10.3897/zookeys.540.9630
Figure 2 - GC-FID/EAD analyses of the Ceratitis fasciventris, Ceratitis anonae, and Ceratitis rosa male-borne volatiles using a conspecific female antenna as an EAD detector. The numbers indicate EAD-active compounds and correspond to Table 1. The symbols EAD-1-3 denote the three independent repetitions of the GC-EAD analyses.
Figure 1 from: Břízová R, Vaníčková L, Faťarová M, Ekesi S, Hoskovec M, Kalinová B (2015) Analyses of volatiles produced by the African fruit fly species complex (Diptera, Tephritidae). 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: 385-404. https://doi.org/10.3897/zookeys.540.9630
Figure 1 - GC×GC-TOFMS chromatograms (TIC mode) of the male (N = 5) volatiles of Ceratitis fasciventris, Ceratitis anonae and Ceratitis rosa. Each spot represents one compound; the identified compounds are numbered in each chromatogram, with the numbering corresponding to the respective Table 1 of compounds. The intensity of each spot is colour-coded (blue - 0, red - maximum).
Figure 3 from: Vaníčková L, Břízová R, Pompeiano A, Ekesi S, De Meyer M (2015) Cuticular hydrocarbons corroborate the distinction between lowland and highland Natal fruit fly (Tephritidae, Ceratitis rosa) populations. 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: 507-524. https://doi.org/10.3897/zookeys.540.9619
Figure 3 - Section of the GC×GC/MS analysis of the female (A) and male (B) cuticular hydrocarbon profiles of coastal population (R1) of Ceratitis rosa from Kenya. The intensity of the signals is colour-coded from green (zero) to red (maximum). The compounds are assigned according to Table 1.
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