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109 results for “Tuerkayana”
Fig. 2 in Tuerkayana latens Ng and Hsi-Te Shih 2023, n. sp.
Fig. 2. Viability of second instar larva to adult for populations of Drosophila willistoni (CAJ, PMA and POA), D. mercatorum (SER, CAJ, SAN and POA), D. maculifrons (CAJ and PMA), and D. ornatifrons (CAJ and PMA). Viability was calculated as the emerged adults/total larvae ratio. Different letters above the bars indicate significant differences at a p value of 0.05 determined by the ANOVA followed by Tukey post-hoc test. Error bars represent standard error of the mean.
Fig. 5 in Tuerkayana latens Ng and Hsi-Te Shih 2023, n. sp.
Fig. 5. Triglycerides (A), Glycogen (B), and Total Protein (C) concentrations per mg of dry weight of adult females and males from populations of Drosophila willistoni (CAJ, PMA, and POA), D. mercatorum (SER, CAJ, SAN, and POA), D. maculifrons (CAJ and PMA), and D. ornatifrons (CAJ and PMA). Values are means and SE for homogenates of 15 flies for D. willistoni and 5 flies for D. mercatorum, D. maculifrons, and D. ornatifrons. Lines above bars group statistically similar values. Asterisks above bars and different letters above lines indicate significant differences (sex and populational, respectively) at a p value of 0.05, determined by the ANOVA followed by Tukey post-hoc test. Error bars represent standard error of the mean.
Fig. 4 in Tuerkayana rotundum
Fig. 4. Whittaker curves showing the rank-abundance relationship of the species registered in the native sites of the province of La Pampa (Parque Luro Provincial Reserve) and Salta (Poligono A Municipal Reserve).
Fig. 3 in Tuerkayana rotundum
Fig. 3. Rarefaction curves based on individuals comparing: a- natural sites of Parque Luro Provincial Reserve (PL) and Poligono A Municipal Reserve (PA); and b- between Parque Luro Provincial Reserve 1 (PL1) and 2 (PL2), selva montana of Poligono A Municipal Reserve (PAM) and selva pedemontana of Poligono A Municipal Reserve (PAP).
Fig. 1 in Tuerkayana latens Ng and Hsi-Te Shih 2023, n. sp.
Fig. 1. Map of the collection areas of Drosophila populations from which isofemale lines were obtained and analyzed. The locations are described in the Material and Methods section. SER: 21°15'15.23"S, 47°34'34.95"W - Altitude 830 m; CAJ: 21°21'35.45"S, 47°17'32.89"W - Altitude 830 m; PMA: 25°21'3.23"S, 51°28'4.41"W - Altitude: 1,000 m; SAN: 29°23'0.54"S, 54°45'41.58"W - Altitude: 135 m; POA: 30°4'9.94"S, 51°7'36.34"W - Altitude: 115 m.
Fig. 5 in Tuerkayana rotundum
Fig. 5. Ordering by CCA analysis of the 12 sampling transects in the natural sites of the province of La Pampa (six circles) and Salta (six triangles), showing a general pattern of relationship with microhabitat environmental variables.
Fig. 3 in Tuerkayana latens Ng and Hsi-Te Shih 2023, n. sp.
Fig. 3. Development time from second instar larva to emerged adults for populations of Drosophila willistoni (CAJ, PMA and POA), D. mercatorum (SER, CAJ, SAN and POA), D. maculifrons (CAJ and PMA), and D. ornatifrons (CAJ and PMA). The development times were measured in hours. Lines above bars group statistically similar values. Asterisks above bars and different letters above lines indicate significant differences (sex and populational, respectively) at a p value of 0.05, determined by the ANOVA followed by Tukey post-hoc test. Error bars represent standard error of the mean.
Fig. 4 in Tuerkayana latens Ng and Hsi-Te Shih 2023, n. sp.
Fig. 4. Dry weights in milligrams of adult females and males from populations of Drosophila willistoni (CAJ, PMA and POA), D. mercatorum (SER, CAJ, SAN and POA), D. maculifrons (CAJ and PMA), and D. ornatifrons (CAJ and PMA). Individual dry weights were calculated from samples of 15 recently emerged flies of D. willistoni, and 5 recently emerged flies of D. mercatorum, D. maculifrons, and D. ornatifrons. Lines above bars group statistically similar values. Asterisks above bars and different letters above lines indicate significant differences (sex and populational, respectively) at a p value of 0.05, determined by the ANOVA followed by Tukey post-hoc test. Error bars represent standard error of the mean.
Fig. 5 in Tuerkayana latens Ng and Hsi-Te Shih 2023, n. sp.
Fig. 5. Currently accepted Cheloniidae relationships and divergence times. The red bar corresponds to the Hyachelia lowryi and H. tortugae divergence time of 26.16 Ma. (95% HPD: 9.36–46.43). Species in bold represent Hyachelia occurrences. Turtle drawings are adapted from Vecta.io and Biorender. Orange triangles represent known H. lowryi hosts and blue dots represent known H. tortugae hosts.
Fig. 4 in Tuerkayana latens Ng and Hsi-Te Shih 2023, n. sp.
Fig. 4. COI+18SrRNA tree of Talitrida based on available sequences. Node values correspond to the estimated divergence time of Hyachelia. Red bars show the 95% highest posterior density. Bootstraps and posterior probability values are represented above branches for the Talitrida, Hyachelia, H. lowryi and H. tortugae. Red horizontal bars correspond to the 95% highest posterior density intervals (HPD). The gray vertical bar corresponds to Chelonioidea radiation according to Kear and Lee (2006).
Fig. 3. Hyachelia tortugae Barnard, 1967 in Tuerkayana latens Ng and Hsi-Te Shih 2023, n. sp.
Fig. 3. Hyachelia tortugae Barnard, 1967 (ZUEC CRU 4386). a, Maxilliped, scale bar: 0.1 mm. b, Gnathopod 2, scale bar: 1.0 mm. c, Uropod 3, scale bar: 0.1 mm. d, Gnathopod 1, scale bar: 0.5 mm. e, Uropod 1, scale bar: 0.5 mm. f, Pereopod 4, scale bar: 0.5 mm. g, Pereopod 7, scale bar: 0.5 mm. h, Uropod 2, scale bar: 1.0 mm.
Fig. 2 in Tuerkayana latens Ng and Hsi-Te Shih 2023, n. sp.
Fig. 2. Hyachelia lowryi Serejo and Sittrop, 2009 (ZUEC CRU 4385). a, Maxilliped, scale bar: 0.1 mm. b, Gnathopod 2, scale bar: 1.0 mm. c, Uropod 3, scale bar: 0.1 mm. d, Gnathopod 1, scale bar: 0.5mm; e) Uropod 1, scale bar: 0.5 mm. f, Pereopod 4, scale bar: 0.5 mm. g, Pereopod 7, scale bar: 0.5 mm; h) Uropod 2, scale bar: 1.0 mm.
Fig. 13 in Tuerkayana latens Ng and Hsi-Te Shih 2023, n. sp.
Fig. 13. Minuca vocator (Herbst, 1804), collected from Curaçao (UNI 713). A: Dorsal view of entire crab. B: Lateral carapace view on side of minor cheliped. C: Outer surface of major cheliped. D: Inner surface of major cheliped. E: Second ambulatory leg. F: Oral view of carapace. a. eyebrow, b. postorbital sulcus, c. dental on suborbital margin, d. anterolateral angle, e. posterolateral line, f. posterolateral striae, g. pubescence, h. articulation ridge, i. pre-pollex depression, j. pollex, k. dactyl, l. superior carpal cavity carina, m. apex of oblique ridge, n. pre-dactyl ridge, o. articulation ridge, p. manus-pollex ridge, q. pubescence, r. setae.
Fig. 6 in Tuerkayana latens Ng and Hsi-Te Shih 2023, n. sp.
Fig. 6. Current known distribution of Hyachelia. Stars correspond to new records, and stars with black outlines correspond to new host records.
Fig. 10 in Tuerkayana latens Ng and Hsi-Te Shih 2023, n. sp.
Fig. 10. Minuca mordax (Smith, 1870), collected from Belize (UNI 47). A: Dorsal view of entire crab. B: Lateral carapace view on side of minor cheliped. C: Outer surface of major cheliped. D: Inner surface of major cheliped. E: Second ambulatory leg. F: Oral view of carapace. a. eyebrow, b. postorbital sulcus, c. suborbital margin, d. anterolateral angle, e. posterolateral line, f. posterolateral striae, h. articulation ridge, j. pollex, k. dactyl, l. superior carpal cavity carina, m. apex of oblique ridge, n. pre-dactyl ridge, o. articulation ridge, q. pubescence, r. setae.
Fig. 12 in Tuerkayana latens Ng and Hsi-Te Shih 2023, n. sp.
Fig. 12. Minuca victoriana (von Hagen, 1987), collected from Vitória, Brazil (UNI 168). A: Dorsal view of entire crab. B: Lateral carapace view on side of minor cheliped. C: Outer surface of major cheliped. D: Inner surface of major cheliped. E: Second ambulatory leg. F: Oral view of carapace. a. eyebrow, b. postorbital sulcus, c. dental on suborbital margin, d. anterolateral angle, e. posterolateral line, f. posterolateral striae, g. pubescence, h. articulation ridge, i. pre-pollex depression, j. pollex, k. dactyl, l. superior carpal cavity carina, m. apex of oblique ridge, n. pre-dactyl ridge, o. articulation ridge, p. manus-pollex ridge, q. pubescence, r. setae.
Fig. 9 in Tuerkayana latens Ng and Hsi-Te Shih 2023, n. sp.
Fig. 9. Other sympatric Minuca from the south Atlantic coast of South America. A: Minuca mordax (Smith, 1870), B: Minuca rapax (Smith, 1870), C: Minuca victoriana von Hagen, 1987. D: Minuca vocator (Herbst, 1804). Adult males, scale bar ≈ 10 mm. Specimens not catalogued.
Fig. 11 in Tuerkayana latens Ng and Hsi-Te Shih 2023, n. sp.
Fig. 11. Minuca rapax (Smith, 1870), collected from Puerto Rico (UNI 421). A: Dorsal view of entire crab. B: Lateral carapace view on side of minor cheliped. C: Outer surface of major cheliped. D: Inner surface of major cheliped. E: Second ambulatory leg. F: Oral view of carapace. a. eyebrow, b. postorbital sulcus, c. dental on suborbital margin, d. anterolateral angle, e. posterolateral line, f. posterolateral striae, h. articulation ridge, j. pollex, k. dactyl, l. superior carpal cavity carina, m. apex of oblique ridge, n. pre-dactyl ridge, o. articulation ridge, p. manus-pollex ridge, q. pubescence, r. setae.
Fig. 1. a in Tuerkayana latens Ng and Hsi-Te Shih 2023, n. sp.
Fig. 1. a, Hawksbill turtle (Eretmochelys imbricata) stranded in Alagoas, northeast Brazil. b, Amphipods (Hyachelia lowryi) associated to E. imbricata, arrow indicates H. lowryi specimens. c, Hyachelia lowryi Serejo and Sittrop, 2009 (ZUEC CRU 4385). d, Hyachelia tortugae Barnard, 1967 (ZUEC CRU 4386).
Fig. 6. Male right G1 in Tuerkayana latens Ng and Hsi-Te Shih 2023, n. sp.
Fig. 6. Male right G1 from Minuca panema (Coelho, 1972) (A, B: MZUSP 20833) and M. burgersi (Holthuis, 1967) (C, D: UNI 719). a. apical flange, b. "thumb" or palp. Scale bar = 0.5 mm.
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