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3,761 results for “phylogenetic relationships”

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FIGURE 12 in A fully web-illustrated morphological phylogenetic study of relationships among oak gall wasps and their closest relatives (Hymenoptera: Cynipidae).

FIGURE 12. Petiole: a Diplolepis triforma, b Neuroterus numismalis parth. gen., c Andricus quercusfoliata, d Biorhiza mellea.

opennotspecifiedJun 2008View details →
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FIGURE 6 in A fully web-illustrated morphological phylogenetic study of relationships among oak gall wasps and their closest relatives (Hymenoptera: Cynipidae).

FIGURE 6. Mesopleuron, lateral view: a Pediaspis aceris parth. gen., b Neuroterus numismalis parth. gen.

opennotspecifiedJun 2008View details →
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FIGURE 2 in A fully web-illustrated morphological phylogenetic study of relationships among oak gall wasps and their closest relatives (Hymenoptera: Cynipidae).

FIGURE 2. Pronotum, anterior view: a Phanacis phoenixopodos, b Trigonaspis gibbera, c Trichagalma serratae.

opennotspecifiedJun 2008View details →
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FIGURE 124 in Phylogenetic relationships of the genera of Epipsocetae (Psocoptera: Psocomorpha)

FIGURE 124. Strict consensus tree of 104 MPTs, generated by removing O. orghidani and P. obscurus (L = 384, IC = 0.41, IR = 0.78). A and B indicate the two main clades topologies for Epipsocidae.

opennotspecifiedMay 2006View details →
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FIGURE 122 in Phylogenetic relationships of the genera of Epipsocetae (Psocoptera: Psocomorpha)

FIGURE 122. Strict consensus of 57189 equally most parsimonious trees (L = 393; IC = 0.40; IR = 0.78).

opennotspecifiedMay 2006View details →
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FIGURES 100–121 in Phylogenetic relationships of the genera of Epipsocetae (Psocoptera: Psocomorpha)

FIGURES 100–121. Ovipositor valvulae and ninth sternum of Dolabellopsocus sp. 3 (100), E pipsocopsis prominens (101) and Euplocania badonneli (102). Gonapophyses of Elipsocus sp. 4 (103), Dichoepipsocus complexus (104), Auroropsocus orientis (105), Hinduipsocus atratus (106), Loneura leonilae (107), Mesepipsocus proctus (108), Epipsocopsis greeni (109) and Valvepipsocus diodematus (110) (from Li Fasheng 2002). Distal process of v2+3 of Euplocania pictaoides (111) and Bertkauia crosbyana (112). Female epiproct of Odontopsocus orghidani (113), Terryerwinia sp. PERU (114), Euplocania pictaoides (115), Goja plaumanni (116) and Mesepipsocus proctus (117). Female paraproct of sp. 3. SABAH (118), Odontopsocus orghidani (119), Cladiopsocus garciai (120) and Epipsocopsis sp. 1 (121).

opennotspecifiedMay 2006View details →
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FIGURES 69–99 in Phylogenetic relationships of the genera of Epipsocetae (Psocoptera: Psocomorpha)

FIGURES 69–99. Hypandrium of Goja montieli (69), Loneura leonilae (70) and Mesepipsocus sp. 15 (71). Phallosome of Euplocania badonneli (72), Triplocania brailovskyana (73), Epipsocus sp. 2 (74), Elipsocus sp. 4 (75), Terryerwinia acutiphallica (76) and Goja montieli (77). External parameres of Mesepipsocus sp. BELICE (78), Bertkauia crosbyana (79), Dolabellopsocus sp. 2 (80), Mesepipsocus sp. 15 (81) and Goja montieli (82). Male clunium, epiproct and paraprocts of E pipsocus sp. 2 (83), Mesepipsocus sp. 15 (84), Dolabellopsocus sp. 2 (85) and Isthmopsocus sp. BE LICE (86). Posterior view of male epiproct of Elipsocus sp. 4 (87), Epipsocus sp. 2 (88) and Dolabellopsocus sp. 3 (89). Anterior view of male epiproct of Elipsocus sp. 4 (90), Hinduipsocus sp. (91), Willreevesia dominica (92) and Euplocania badonneli (93). Male paraproct of Cladiopsocus ocotensis (94). Posterior view of subgenital plate of Goja montieli (95), Dolabellopsocus sp. 2 (96), Mesepipsocus proctus (97), Bertkauia crosbyana (98) and Hinduipsocus atratus (99).

opennotspecifiedMay 2006View details →
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FIGURES 33–68 in Phylogenetic relationships of the genera of Epipsocetae (Psocoptera: Psocomorpha)

FIGURES 33–68. Female hind coxa of Hinduipsocus atratus (33) and Cladiopsocus ocotensis (34). Ventral surface of fore femur of Goja montieli (35), Epipsocopsis prominens (36) and Auroropsocus orientis (37). Tarsus of Bertkauia crosbyana (38), Dolabellopsocus sp. 2 (39) and E lipsocus sp. 4 (40). Pretarsal claw of Dichoepipsocus micropterus (41), Ianthorntonia annae (42), Cladiopsocus ocotensis (43) and Isthmopsocus sp. 2 (44). Female fore wing of Goja montieli (45) and Hinduipsocus sp. (46). Middle view of forewing of Elipsocus sp. 4 (47). Forewing of E pipsocus sp. 2 (48), Incapsocus penai (49), Goja montieli (50) and Ptiloneura bidorsalis (51). Hindwing of Stenopsocus immaculatus (52) and Goja montieli (53). Pterostigma of Dolabellopsocus sp. 2 (54), Bertkauia crosbyana (55), Neurostigma enderleini (56) and Spurostigma sp. 2 (57). Areola postica of Dolabellopsocus sp. 2 (58), Bertkauia crosbyana (59), Stenopsocus immaculatus (60), Auroropsocus orientis (61) and Neurostigma enderleini (62). Posterior view of forewing of Euplocania badonneli (63). Anal margin of forewing of Spurostigma sp. 2 (64), Isthmopsocus sp. (65) and Auroropsocus orientis (66). Costal margin of hindwing of Stenopsocus immaculatus (67) and Euplocania badonneli (68).

opennotspecifiedMay 2006View details →
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FIGURE 123 in Phylogenetic relationships of the genera of Epipsocetae (Psocoptera: Psocomorpha)

FIGURE 123. Consensus tree showing the character states that can be unambiguously optimized in all the MPTs. Black bars are apomorphic characters and grey bars are homoplastic characters. The arrow (?) indicates that the cladogram continues in the next page.

opennotspecifiedMay 2006View details →
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FIGURES 1–32 in Phylogenetic relationships of the genera of Epipsocetae (Psocoptera: Psocomorpha)

FIGURES 1–32. Compound eye of Bertkauia crosbyana (1), Isthmopsocus sp. 2 (2) and Goja montieli (3). Frons of Dolabellopsocus sp. 2 (4). Ocelli of Elipsocus sp. 4 (5), Epipsocus sp. 2 (6), Goja montieli (7) and Isthmopsocus sp. 2 (8). Scape and pedicel of Dicropsocus montanus (9) and loneura leonilae (10). Front view of head of Cladiopsocus ocotensis (11) and Triplocania brailovskyana (12). Anterior ends of epistomal suture of Euplocania badonneli (13) and Goja plaumanni (14). Labrum of Stenopsocus immaculatus (15), Dolabellopsocus sp. 2 (16), Bertkauia crosbyana (17) and Cladiopsocus ocotensis (18). Distal inner labral sensilla of Elipsocus sp. 4 (19) and Ianthorntonia annae (20). Anterior ends of labrum of Cladiopsocus garciai (21) and labral tubercles of Ianthorntonia annae (22), Terryerwinia acutiphallica (23) and Mesepipsocus sp. 1 (24). Right mandible of Spurostigma sp. 2 (25) and Ianthorntonia annae (26). Lacinial apex of Stenopsocus immaculatus (27), Dolabellopsocus sp. 2 (28), Epipsocopsis greeni (29), Dicropsocus complexus (30), Dichoepipsocus micropterus (31) and Ianthorntonia annae (32).

opennotspecifiedMay 2006View details →
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FIGURE 125 in Phylogenetic relationships of the genera of Epipsocetae (Psocoptera: Psocomorpha)

FIGURE 125. Phylogenetic relationships among genera of Epipsocetae and sister families. Question marks (?) indicate that monophyly is not supported.

opennotspecifiedMay 2006View details →
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F in Frenguelliidae, a new family of dragonflies from the earliest Eocene of Argentina (Insecta: Odonata): phylogenetic relationships within Odonata

F. 3. Interpretation of Frenguellia patagonica gen. nov., sp. n. holotype MLP 6431, detail of nodal structures (scale=0.5 mm). Arrows show the zigzagged portion of RA and the posterior displacement of ScP due to biostratinomic deformation.

opennotspecifiedDec 2003View details →
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F in Frenguelliidae, a new family of dragonflies from the earliest Eocene of Argentina (Insecta: Odonata): phylogenetic relationships within Odonata

F. 1. Photograph of Frenguellia patagonica gen. nov., sp. n. holotype MLP 6431, general habitus (scale=3 mm).

opennotspecifiedDec 2003View details →
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F in Frenguelliidae, a new family of dragonflies from the earliest Eocene of Argentina (Insecta: Odonata): phylogenetic relationships within Odonata

F. 2. Interpretation of Frenguellia patagonica gen. nov., sp. n. holotype MLP 6431, general habitus (scale=3 mm). Arrow shows the distal displacement of RA due to biostratinomic deformation.

opennotspecifiedDec 2003View details →
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FIGURE 4 in Limits and phylogenetic relationships of East Asian fishes in the subfamily Oxygastrinae (Teleostei: Cypriniformes: Cyprinidae)

FIGURE 4. The strict consensus of four most-parsimonious trees (length = 25370 steps; CI = 0.159; RI = 0.460) based on a data matrix with a subset of 122 taxa (of 144); terminals represented solely by sequences obtained from GenBank were removed. Bootstrap values are reported at each node (values below 50% are not shown).

opennotspecifiedJun 2013View details →
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FIGURE 2a in Limits and phylogenetic relationships of East Asian fishes in the subfamily Oxygastrinae (Teleostei: Cypriniformes: Cyprinidae)

FIGURE 2a. The phylogenetic relationships of the subfamily Oxygastrinae, as represented by the strict consensus of six mostparsimonious trees (length = 26366 steps; CI = 0.154; RI = 0.469). Relationships are shown for (a) outgroup taxa and (b) subfamily Oxygastrinae. Bremer (above) and bootstrap (below) support values are displayed at each node (bootstrap values below 50% are not shown).

opennotspecifiedJun 2013View details →
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FIGURE 3 in Limits and phylogenetic relationships of East Asian fishes in the subfamily Oxygastrinae (Teleostei: Cypriniformes: Cyprinidae)

FIGURE 3. The tree topology with the best log likelihood score (ln L = -107719.569) resulting from 100 independent searches of a data matrix with a subset of 122 taxa (of 144); terminals represented solely by sequences obtained from GenBank were removed. Bootstrap values are reported at each node (values below 50% are not shown).

opennotspecifiedJun 2013View details →
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FIGURE 1a in Limits and phylogenetic relationships of East Asian fishes in the subfamily Oxygastrinae (Teleostei: Cypriniformes: Cyprinidae)

FIGURE 1a. The phylogenetic relationships of the subfamily Oxygastrinae (Teleostei: Cypriniformes: Cyprinidae), as represented by the tree topology with the best log likelihood score (ln L = -111857.327) recovered from 100 independent maximum likelihood searches. Bootstrap values are reported at each node (values below 50% are not shown). Relationships are shown for (a) outgroup taxa and (b) subfamily Oxygastrinae.

opennotspecifiedJun 2013View details →
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FIGURE 2b in Limits and phylogenetic relationships of East Asian fishes in the subfamily Oxygastrinae (Teleostei: Cypriniformes: Cyprinidae)

FIGURE 2b. The phylogenetic relationships of the subfamily Oxygastrinae, as represented by the strict consensus of six mostparsimonious trees (length = 26366 steps; CI = 0.154; RI = 0.469). Relationships are shown for (a) outgroup taxa and (b) subfamily Oxygastrinae. Bremer (above) and bootstrap (below) support values are displayed at each node (bootstrap values below 50% are not shown).

opennotspecifiedJun 2013View details →
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Figure 51. Character states for characters 31 in The comparative osteology and phylogenetic relationships of African and South American lungfishes (Sarcopterygii: Dipnoi)

Figure 51. Character states for characters 31 (contact between pterygoid tooth plates) and 33 (number of ridges on tooth plate). Pterygoid tooth plates in ventral view of: A, Neoceratodus forsteri, AMS I-40438-001; B, †Arganodus atlantis, KU 60708; and C, Protopterus aethiopicus, UF 137272. Anterior is to the top. †Dagger symbol represents extinct taxa. Scale bars: 5 mm.

opennotspecifiedMar 2015View details →

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