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Figure 90-91 in Monographic revision of the genus Aegidinus Arrow (1904) and generic phylogeny of the world Orphninae (Coleoptera: Scarabaeidae: Orphninae).
Figure 90-91. Aegidinus oreibates female. Scale bar = 1 mm. 90) Dorsal habitus. Arrow indicates depression. 91) Lateral habitus.
Figure 83- 87 in Monographic revision of the genus Aegidinus Arrow (1904) and generic phylogeny of the world Orphninae (Coleoptera: Scarabaeidae: Orphninae).
Figure 83- 87. Scale bar = 1 mm. 83) Lateral 3/4 habitus of A. cornutus. Arrow indicates tubercle. 84) Dorsal habitus of A. crypticus. 85) Lateral habitus of A. crypticus. Arrow indicates boss. 86) Lateral 3/4 habitus of A. guianensis. Arrow indicates tumosity.87) Dorsal habitus of A. guianensis. Arrow indicates fovea.
Figures 78-81. 78 in Monographic revision of the genus Aegidinus Arrow (1904) and generic phylogeny of the world Orphninae (Coleoptera: Scarabaeidae: Orphninae).
Figures 78-81. 78) Elytra of Aegidinus sp. Arrow indicates transverse row of U- or V- shaped, impressed lines. 79) Lateral view of elytra. Arrow indicates location of margin adjacent to humerus. 80) Procoxa (dorsal surface), showing two setose pits. 81) Ventral view of A. oreibates female.
Figures 65-77 in Monographic revision of the genus Aegidinus Arrow (1904) and generic phylogeny of the world Orphninae (Coleoptera: Scarabaeidae: Orphninae).
Figures 65-77. Female genitalia, gonocoxites. Scale bar = 1 mm. 65) A. brasiliensis. 66) A. candezei. 67) A. guianensis. 68) A. howdenorum. 69) A. howeae. 70) A. oreibates. 71) A. simulatus. 72) A. sunidigea. 73-74) A. teamscaraborum. 75) A. tricornus. 76) A. unicus. 77) A. venezuelensis.
Figures 50- 64 in Monographic revision of the genus Aegidinus Arrow (1904) and generic phylogeny of the world Orphninae (Coleoptera: Scarabaeidae: Orphninae).
Figures 50- 64. Male genitalia. Scale bar = 1 mm. 50) Parameres (frontal view) of A. guianensis. 51) Parameres and part of phallobase (lateral view) of A. guianensis. 52) Parameres (frontal view) of A. howdenorum. 53) Parameres and part of phallobase (lateral view) of A. howdenorum. 54) Ventral plate of A. howdenorum. 55) Lateral lobe of A. howdenorum. Arrow indicates notch. 56) Parameres (frontal view) of A. howeae. 57) Parameres and part of phallobase (lateral view) of A. howeae. 58) Parameres (frontal view) of A. oreibates. 59) Parameres and portion of phallobase (lateral view) of A. oreibates. 60) Ventral plate of A. oreibates. 61) Parameres (frontal view) of A. petrovi. 62) Parameres and part of phallobase (lateral view) of A. petrovi. 63) Parameres (frontal view) of A. teamscaraborum. 64) Parameres and part of phallobase (lateral view) of A. teamscaraborum.
Figure 30 in Monographic revision of the genus Aegidinus Arrow (1904) and generic phylogeny of the world Orphninae (Coleoptera: Scarabaeidae: Orphninae).
Figure 30. Strict consensus tree of the Orphninae showing separate Old and New World clades (excludes Stenosternus costatus and Goniorphnus felschei). Bootstrap values are shown on tree.
Figure 29 in Monographic revision of the genus Aegidinus Arrow (1904) and generic phylogeny of the world Orphninae (Coleoptera: Scarabaeidae: Orphninae).
Figure 29. Strict consensus tree of the Orphninae, including all taxa. Boot strap values are shown on tree.
Figure 1-9 in Monographic revision of the genus Aegidinus Arrow (1904) and generic phylogeny of the world Orphninae (Coleoptera: Scarabaeidae: Orphninae).
Figure 1-9. Scale bar = 1 mm. 1) Mouthparts exposed beyond clypeus. a) Labrum exposed beyond edge of clypeus. b) Single, external, lateral lobe on mandibles. 2) Apical spines of metatibia (indicated by arrows) separated by basal metatarsal segment. 3) Female genital sclerites of Aegidinus brasiliensis Arrow. a) Superior sclerite. b) Inferior sclerite. c) Interior process. 4). Female genital sclerites of A. oreibates Colby. a) Superior sclerite. b) Inferior sclerite. c) Accessory sclerite. 5) Male parameres (frontal view) of A. oreibates. a) Lateral lobe. b) Median lobe. 6) Male parameres (frontal view) of A. brasiliensis. a) Lateral lobe. b) Median lobe. 7) Male parameres and phallobase (lateral view) of A. guianensis (Westwood). a) Lateral lobe. b) Median lobe. c) phallobase. d) Basal piece of phallobase. 8) Attachment of first antennal club segment to stem offset (Hybalus sp.). 9) Attachment of first antennal club segment to stem not offset (Orphnus sp.).
Figures 38-49 in Monographic revision of the genus Aegidinus Arrow (1904) and generic phylogeny of the world Orphninae (Coleoptera: Scarabaeidae: Orphninae).
Figures 38-49. Male genitalia. Scale bar = 1 mm. 38) Parameres (frontal view) of Aegidinus brasiliensis. 39) Parameres and part of phallobase (lateral view) of A. brasiliensis. 40) Parameres (frontal view) of A. candezei. 41) Parameres and part of phallobase (left, lateral view) of A. candezei. 42) Ventral plate of A. candezei. 43) Parameres and part of phallobase (right, lateral view) of A. candezei. 44) Parameres (frontal view) of A. cornutus. 45) Parameres and part of phallobase (lateral view) of A. cornutus. 46) Parameres (frontal view) of A. crypticus. 47) Parameres and part of phallobase (lateral view) of A. crypticus. 48) Ventral plate of A. crypticus.49) Lateral lobe of A. crypticus.
Figures 34-37. 34 in Monographic revision of the genus Aegidinus Arrow (1904) and generic phylogeny of the world Orphninae (Coleoptera: Scarabaeidae: Orphninae).
Figures 34-37. 34) Aegidium sp. male dorsal view. 35) Aegidium sp. female, dorsal view. 36) Aegidiellus alatus male, dorsal view. 37) Aegidiellus alatus female, dorsal view.
Figures 22-28 in Monographic revision of the genus Aegidinus Arrow (1904) and generic phylogeny of the world Orphninae (Coleoptera: Scarabaeidae: Orphninae).
Figures 22-28. All scale bars = 1 mm. 22) Abdomen of Aegidinus sp. Arrows indicate stridulatory combs. 23) Completely sclerotized phallobase of Aegidinus howdenorum (ventral view). 24) Incompletely sclerozited phallobase of Hybalus sp. (ventral view). 25) Spiculum gastrale (Orphnus sp.) harp- shaped. 26) Spiculum gastrale (Chaetonyx robustus) wishbone- shaped. 27) Spiculum gastrale (Aegidium sp.) t- shaped. 28) Madecorphnus sp. phallobase (dorsal view). Arrow indicates bulge.
Figure 15-21 in Monographic revision of the genus Aegidinus Arrow (1904) and generic phylogeny of the world Orphninae (Coleoptera: Scarabaeidae: Orphninae).
Figure 15-21. Scale bar = 1 mm. 15) Prefemoral cleaning brush composed of a line of setae (Madecorphnus sp.). 16) Prefemoral cleaning brush composed of a patch of setae (Aegidium sp.). 17) Prefemoral cleaning brush composed of a line and a patch of setae (Orphnus sp.). 18) Mesofemur without ridge along posterior edge (Aegidiellus alatus). 19) Mesofemur with ridge along posterior edge; surface posterior to ridge minutely roughened (Aegidium sp.). Arrow indicates position of ridge. 20) Ventral view of Brenskea coronata. a) Mesocoxae contiguous. b) Mesometasternum unsutured. 21) Ventral view of Orphnus sp. a) Mesocoxae separated. b) Meso- metasternum sutured.
Figure 31-33. Paraegidium costalimai. 31 in Monographic revision of the genus Aegidinus Arrow (1904) and generic phylogeny of the world Orphninae (Coleoptera: Scarabaeidae: Orphninae).
Figure 31-33. Paraegidium costalimai. 31) Clypeus (frontal view). 32) Dorsal habitus of female. Note vermiform punctures on pronotum and U- shaped punctures on elytra. 33) Dorsal habitus of male.
Figure 10-14. 10 in Monographic revision of the genus Aegidinus Arrow (1904) and generic phylogeny of the world Orphninae (Coleoptera: Scarabaeidae: Orphninae).
Figure 10-14. 10) Mandible of Aegidinus sp. Arrow indicates single, external, lateral lobe. Scale bar = 100 m. 11) Mandible of Aclopus sp. Scale bar = 1 mm. 12) Mandible of Aegidium sp. a) Mesal mandibular brush. b) Mandibular prostheca. Scale bar = 1 mm. 13) Galea of Paraegidium sp. Arrow indicates trapezoidal distagalea. 14) Protibia of Aegidinus sp. Arrow indicates apical denticle. Scale bar = 1 mm.
Fig. 65 in Phylogeny Of Phyllostomid Bats (Mammalia: Chiroptera): Data From Diverse Morphological Systems, Sex Chromosomes, And Restriction Sites
Fig. 65. Evolution of carnivory inferred from our optimization of the carnivory character of Ferrarezi and Gimenez (1996: table 1; see our table 8) on our strict consensus tree from the character congruence analysis. The ''uncertain'' states for Phyllostomus and Tonatia are due to taxonomic polymorphism.
Fig. 64 in Phylogeny Of Phyllostomid Bats (Mammalia: Chiroptera): Data From Diverse Morphological Systems, Sex Chromosomes, And Restriction Sites
Fig. 64. Evolution of different types of nectarivory inferred from our optimization of the nectarivory character of Ferrarezi and Gimenez (1996: table 1; see our table 8) on our strict consensus tree from the character congruence analysis. Note that the nectarivory character, as defined by Ferrarezi and Gimenez (1996) includes the consumption of pollen and petals. To prevent an equivocal reconstruction for the base of the clade that includes all phyllostomids except desmodontines, we examined trees in which the position of Brachyphylla was resolved and fixed the node at the base of the clade that includes all phyllostomids except desmodontines with the state that occurred under the two alternative placements for this genus.
Fig. 63 in Phylogeny Of Phyllostomid Bats (Mammalia: Chiroptera): Data From Diverse Morphological Systems, Sex Chromosomes, And Restriction Sites
Fig. 63. Evolution of different types of frugivory inferred from our optimization of the frugivory character of Ferrarezi and Gimenez (1996: table 1; see our table 8) on our strict consensus tree from the character congruence analysis. To prevent an equivocal reconstruction for the base of the clade that includes all phyllostomids except desmodontines, we examined trees in which the position of Brachyphylla was resolved and fixed the node at the base of the clade that includes all phyllostomids except desmodontines with the state that occurred under the two alternative placements for this genus.
Fig. 62 in Phylogeny Of Phyllostomid Bats (Mammalia: Chiroptera): Data From Diverse Morphological Systems, Sex Chromosomes, And Restriction Sites
Fig. 62. Evolution of different types of insectivory (see text for description of character states) inferred from our optimization of the insectivory character of Ferrarezi and Gimenez (1996: table 1; see our table 8) on our strict consensus tree from the character congruence analysis. We inferred the state at the root with reference to a phylogeny of Microchiroptera (Simmons, 1998). The equivocal optimizations for Phyllostomidae and Vampyrini are due to differences in interpretation of the character under ACCTRAN or DELTRAN. The ''uncertain'' state for Noctilio is due to taxonomic polymorphism (see table 8).
Fig. 61 in Phylogeny Of Phyllostomid Bats (Mammalia: Chiroptera): Data From Diverse Morphological Systems, Sex Chromosomes, And Restriction Sites
Fig. 61. Tree used by Ferrarezi and Gimenez (1996; redrawn from fig. 4) with their feedinghabits character optimized on the topology. This character was ordered such that predominant insectivory evolved from strict insectivory; predominant carnivory, predominant frugivory, or sanguivory evolved from predominant insectivory; and predominant nectarivory or strict frugivory evolved from predominant frugivory.
Fig. 60 in Phylogeny Of Phyllostomid Bats (Mammalia: Chiroptera): Data From Diverse Morphological Systems, Sex Chromosomes, And Restriction Sites
Fig. 60. Evolution of the labial horseshoe inferred from optimization of character 25 on the strict consensus tree from our character congruence analysis. The morphology of the thickened labial horseshoe (character 27) is also indicated: asterisks indicate taxa with a Vshaped labial projection; a single cross indicates taxa in which all individuals have a Vshaped notch; a double cross indicates taxa in which some individuals have a Vshaped notch. The state for Centurio is not indicated because we scored this taxon ''?'' for all characters related to the noseleaf (see character 18).
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