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32 results for “Cuculidae”
Figure 1 in The haemoproteids of the Cuculidae
Figure 1. (A–C) Haemoproteus cuculis sp. nov.: (A) immature gametocyte; (B) macrogametocyte; (C) microgametocyte (upper) and immature gametocyte (lower). (D–F) Haemoproteus centropi: (D) immature gametocyte (upper) and almost mature microgametocyte (lower); (E) macrogametocyte; (F) two microgametocytes. (G–I) Haemoproteus clamatori sp. nov.: (G) immature gametocyte; (H) macrogametocyte; (I) microgametocyte. Scale bar: 14 mm.
Fig. 2 in A new species of Centrorhynchus (Acanthocephala, Centrorhynchidae) endoparasite of Guira guira (Aves, Cuculidae) from Argentina
Fig. 2. SEM micrographs of Centrorhynchus guira n. sp.: a - proboscis armament, lateral view; b - proboscis armament, apical view, showing longitudinal rows with 19 hooks per row (arrow); c - female, posterior end; d - male, posterior end with everted copulatory bursa; e - internal anatomy showing an apparent segmentation.
Fig. 1 in A new species of Centrorhynchus (Acanthocephala, Centrorhynchidae) endoparasite of Guira guira (Aves, Cuculidae) from Argentina
Fig. 1. Microphotographs of Centrorhynchus guira n. sp. a - proboscis armament; b - detail of transitional hooks; c - female, reproductive system; d - female, posterior end; e - male, posterior end with everted copulatory bursa; f - detail of uterine bell; g - detail of uterus; h - vagina showing 2 sphincters; i - egg, superficial view; j - egg, detail of acanthor and middle shell without polar prolongations.
Figure 3. After extracting a in Observations Of Novel Feeding Tactics In Guira Cuckoo Guira Guira (Aves: Cuculidae)
Figure 3. After extracting a larva the cuckoos descended to the ground to soften it up before consumption.
Figure 2 in Observations Of Novel Feeding Tactics In Guira Cuckoo Guira Guira (Aves: Cuculidae)
Figure 2. Guira Cuckoo Guira guira inserting its bill into the silk nest of Brassolis sophorae to extract a larva.
Figure 1 in Observations Of Novel Feeding Tactics In Guira Cuckoo Guira Guira (Aves: Cuculidae)
Figure 1. Mature larva of Brassolis sophorae.
FIGURE 3 in New feather mites of the genera Aniacarus and Aniibius (Acariformes: Pterolichidae) from two cuckoo species (Cuculiformes: Cuculidae) in Brazil
FIGURE 3. Aniacarus ani sp. n., details. A–D—legs I–IV of male, respectively, E—tarsus and tibia IV of female, F—spermatheca.
FIGURE 9 in New feather mites of the genera Aniacarus and Aniibius (Acariformes: Pterolichidae) from two cuckoo species (Cuculiformes: Cuculidae) in Brazil
FIGURE 9. Aniacarus robustus sp. n., details. A—leg I of male, B—leg II of male, C—tibia and tarsus IV of male, D—adanal sucker, E—spermatheca.
FIGURE 6 in New feather mites of the genera Aniacarus and Aniibius (Acariformes: Pterolichidae) from two cuckoo species (Cuculiformes: Cuculidae) in Brazil
FIGURE 6. Aniacarus simplex sp. n., details. A—leg I of male, B—leg II of male, C—tibia and tarsus IV of male, D—spermatheca.
FIGURE 12 in New feather mites of the genera Aniacarus and Aniibius (Acariformes: Pterolichidae) from two cuckoo species (Cuculiformes: Cuculidae) in Brazil
FIGURE 12. Aniacarus coronatus sp. n., details. A—leg I of male, B—leg II of male, C—tibia and tarsus IV of male, D—femur, genu and tibia I of male, E—gnathosoma of male, dorsal view, F—spermatheca.
FIGURE 15 in New feather mites of the genera Aniacarus and Aniibius (Acariformes: Pterolichidae) from two cuckoo species (Cuculiformes: Cuculidae) in Brazil
FIGURE 15. Aniibius guirae sp. n., details. A–D—legs I–IV of male, respectively, E—genital apparatus, F—genu II of female, G—spermatheca. Scale bars: A–F—50 µm, G—25 µm.
FIGURE 2 in Integrating voice and phenotype in a revision of the brush cuckoo Cacomantis variolosus (Aves: Cuculidae) complex
FIGURE 2. The seven element shapes found in the Cacomantis variolosus complex. Taxon names given represent the following geographic song types (see Results): sepulcralis—Sundaland and Philippines, virescens—Sulawesi and Sula, aeruginosus—resident Moluccas, variolosus—Australasia, blandus—Admiralty Islands, addendus—Solomon Islands.
FIGURE 4 in Integrating voice and phenotype in a revision of the brush cuckoo Cacomantis variolosus (Aves: Cuculidae) complex
FIGURE 4. Boxplots of vocal measurements. Explanation of variables: pacing—elements per second; element duration in seconds; changes in center frequency in Hertz. For further explanation of vocal parameters, see Methods.
FIGURE 3 in Integrating voice and phenotype in a revision of the brush cuckoo Cacomantis variolosus (Aves: Cuculidae) complex
FIGURE 3. Principal component analysis plot based on the four vocal parameters measured. The first principal component (PC1) chiefly differentiates addendus and virescens, while the second PC splits the sepulcralis group and variolosus group. The inferred Australian migrant variolosus individual (ML 168559) found on Flores, Nusa Tenggara, Indonesia, is denoted by an arrow.
FIGURE 1 in Integrating voice and phenotype in a revision of the brush cuckoo Cacomantis variolosus (Aves: Cuculidae) complex
FIGURE 1. Distribution of the Cacomantis variolosus complex across the Indo-Pacific region: (a) showing the ranges of taxa listed in Table 1; (b) showing all species and subspecies recognized as a result of this study, with species encircled.
Figure 6 in Three terrestrial Pleistocene coucals (Centropus: Cuculidae) from southern Australia: biogeographical and ecological significance
Figure 6. Body mass estimates for extant cuculids, using eight regression equations derived from Campbell & Marcus (1992); estimates are expressed as a proportion of published mean body mass for each species (Dunning, 2008; Erritzøe et al., 2012) (e.g. a value of 2 on the y-axis indicates that the estimated body mass is double the average for that species). Abbreviations: C., Centropus; E., Eudynamys; S., Scythrops.
Figure 9 in Three terrestrial Pleistocene coucals (Centropus: Cuculidae) from southern Australia: biogeographical and ecological significance
Figure 9. Subtrees of the phylogeny shown in Figure 8, showing differences in topology amongst the 16 shortest trees on which the consensus tree is based (topologies shown at A, B, C, and D were each recovered four times). Changes in the positions of Coua, Centropus phasianinus, Centropus violaceus, and Centropus maximus sp. nov. show that there was conflict in the relationships of the Centropus and Coua taxa.
Figure 4 in Three terrestrial Pleistocene coucals (Centropus: Cuculidae) from southern Australia: biogeographical and ecological significance
Figure 4. Referred material of Centropus bairdi sp. nov. from Leaena's Breath Cave, Nullarbor Plain, south-central Australia. Right tibiotarsus WAM 09.3.279 in cranial (A) and caudal (B) aspects; left tarsometatarsus WAM 09.3.280 in dorsal (C), plantar (D), and proximal (E) aspects; left tarsometatarsus of Centropus phasianinus MV B.12969 (F) in plantar aspect provided for comparison. Abbreviations: ccl, crista cnemialis lateralis; cf, crista fibularis; cl, condylus lateralis; cm, cotyla medialis; ei, eminentia intercotylaris; fg, facies gastrocnemialis; fdl, canal for tendon of m. flexor digitorum longus; fhl, canal for tendon of m. flexor hallucis longus; fpht, fossa parahypotarsalis medialis; fvp, foramina vascularia proximalia; ii, incisura intercondylaris; ps, pons supratendineus; se, sulcus extensorius; sf, sulcus flexorius; tfb, tuberculum m. fibularis brevis; ttc, tuberositas m. tibialis cranialis. Scale bars = 1 cm.
Figure 1 in Three terrestrial Pleistocene coucals (Centropus: Cuculidae) from southern Australia: biogeographical and ecological significance
Figure 1. Map of key localities mentioned in the text, showing the range of extant Centropus phasianinus, and showing landbridge connections between Australia and Melanesia at different Pleistocene sea level low-stands (–40 and –130 m) relative to modern sea level; (modified from Sahul and Sunda Shelf Basemap, CartoGIS CAP, 2013, Map 00-101; downloaded from http://asiapacific.anu.edu.au/mapsonline/base-maps/sunda-and-sahul-shelf, 08-05-2015).
Figure 8 in Three terrestrial Pleistocene coucals (Centropus: Cuculidae) from southern Australia: biogeographical and ecological significance
Figure 8. Phylogeny of cuculids, including the extinct Australian species, Centropus maximus sp. nov., based upon the 135-character osteological phylogeny of Hughes (2000); bootstrap consensus of 16 shortest trees (tree length = 308, consistency index = 0.59, retention index = 0.87); numbers above branches/nodes are bootstrap support values, expressed as percentages; taxon names in parentheses reflect current synonyms of taxa included in Hughes's (2000) original analysis.
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