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Journal articles on the topic 'Pig-nosed turtle'

Author: Grafiati

Published: 4 June 2021

Last updated: 5 February 2022

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1

Georges, Arthur, Erika Alacs, Matthew Pauza, Felix Kinginapi, Amos Ona, and Carla Eisemberg. "Freshwater turtles of the Kikori Drainage, Papua New Guinea, with special reference to the pig-nosed turtle, Carettochelys insculpta." Wildlife Research 35, no. 7 (2008): 700. http://dx.doi.org/10.1071/wr07120.

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A survey of the Kikori River drainage of the Gulf Province of Papua New Guinea identified four species of freshwater turtle. The pig-nosed turtle Carettochelys insculpta and the southern New Guinea soft-shelled turtle Pelochelys bibroni are riverine species. The New Guinea spotted turtle Elseya novaeguineae lives primarily in the tidal freshwater creeks and streams, flooded sinkholes and swamps of the lowland rainforest. The New Guinea painted turtle Emydura subglobosa resides almost exclusively in forest sinkholes and swamps. Pelochelys bibroni was the least-common species, and is probably lo

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2

Eisemberg, Carla C., Mark Rose, Benedict Yaru, and Arthur Georges. "Spatial and temporal patterns of harvesting of the Vulnerable pig-nosed turtle Carettochelys insculpta in the Kikori region, Papua New Guinea." Oryx 49, no. 4 (2014): 659–68. http://dx.doi.org/10.1017/s0030605313001646.

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AbstractManagement of wildlife use by communities living a partially traditional lifestyle is usually more successful when the interactions between those communities and the environment are well understood. We mapped the harvest areas for the Vulnerable pig-nosed turtle Carettochelys insculpta for six language-groups in the Kikori region of Papua New Guinea and compared harvest parameters between different areas and language-groups and, when possible, between 1980–1982 and 2007–2009. Spatially, the main influence on harvest method was a tribe's location relative to the turtle's distribution. N

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3

Doody, J. Sean, Arthur Georges, Jeanne E. Young, et al. "Embryonic aestivation and emergence behaviour in the pig-nosed turtle, Carettochelys insculpta." Canadian Journal of Zoology 79, no. 6 (2001): 1062–72. http://dx.doi.org/10.1139/z01-061.

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Two related aspects of hatchling emergence were studied in a population of pig-nosed turtles (Carettochelys insculpta) in northern Australia. Using emergence phenology data, nest temperatures, historical weather data, and a developmental model, we tested the hypothesis that delayed hatching occurs in C. insculpta, and that such a delay would allow hatchlings to time their emergence to match the onset of the wet season. Carettochelys insculpta hatchlings emerged, on average, 17 days after dates predicted from a developmental model. Combined with observations of hatchlings remaining in eggs unti

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4

Doody, J. S., B. Green, R. Sims, D. Rhind, P. West, and D. Steer. "Indirect impacts of invasive cane toads (Bufo marinus) on nest predation in pig-nosed turtles (Carettochelys insculpta)." Wildlife Research 33, no. 5 (2006): 349. http://dx.doi.org/10.1071/wr05042.

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The cane toad (Bufo marinus) was introduced into Australia in 1935. Because this toxic frog is novel to the Australian fauna, its introduction has impacted native fauna in a variety of ways. We anticipated a severe decline in the yellow-spotted monitor lizard (Varanus panoptes) associated with the arrival of cane toads along the Daly River, Northern Territory, and predicted a simultaneous impact on nest predation in the pig-nosed turtle (Carettochelys insculpta) because the lizard is the chief predator of C. insculpta eggs at the site. We surveyed for monitors and cane toads for five years at

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5

Doody, J. Sean, Matthew Pauza, Bret Stewart, and Chris Camacho. "Nesting Behavior of the Pig-Nosed Turtle, Carettochelys insculpta, in Australia." Chelonian Conservation and Biology 8, no. 2 (2009): 185–91. http://dx.doi.org/10.2744/ccb-0764.1.

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6

Ferrara, Camila R., Richard C. Vogt, Carla C. Eisemberg, and J. Sean Doody. "First Evidence of the Pig-nosed Turtle (Carettochelys insculpta) Vocalizing Underwater." Copeia 105, no. 1 (2017): 29–32. http://dx.doi.org/10.1643/ce-16-407.

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7

Xiong, Lei, Xiao-san Li, Ling Wang, Ke Zhou, and Liu-wang Nie. "The mitochondrial genome complete sequence and organization of the Pig-nosed Turtle Carettochelys insculpta (Testudines, Carettochelyidae) and its phylogeny position in Testudines." Amphibia-Reptilia 31, no. 4 (2010): 541–51. http://dx.doi.org/10.1163/017353710x530203.

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AbstractThe Pig-nosed Turtle Carettochelys insculpta (Testudines; Cryptodira; Carettochelyidae) is the sole living representative of the Carettochelyidae. The phylogenetic position of C. insculpta within Testudines has not yet been determined unequivocally. To address this issue, we sequenced the whole mitochondrial DNA (mtDNA) of C. insculpta using the long-and-accurate PCR (LA-PCR) method. The results show that the length of C. insculpta mtDNA is 16 439 bp and its structure is conserved compared to those of other turtles and other vertebrates except the NADH4 gene beginning with an ATC start

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8

Rivera, Angela R. V., and Richard W. Blob. "Forelimb muscle function in pig-nosed turtles, Carettochelys insculpta : testing neuromotor conservation between rowing and flapping in swimming turtles." Biology Letters 9, no. 5 (2013): 20130471. http://dx.doi.org/10.1098/rsbl.2013.0471.

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Changes in muscle activation patterns can lead to new locomotor modes; however, neuromotor conservation—the evolution of new forms of locomotion through changes in structure without concurrent changes to underlying motor patterns—has been documented across diverse styles of locomotion. Animals that swim using appendages do so via rowing (anteroposterior oscilations) or flapping (dorsoventral oscilations). Yet few studies have compared motor patterns between these swimming modes. In swimming turtles, propulsion is generated exclusively by limbs. Kinematically, turtles swim using multiple styles

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9

Beggs, Kerry, Jeanne Young, Arthur Georges, and Peter West. "Ageing the eggs and embryos of the pig-nosed turtle, Carettochelys insculpta (Chelonia: Carettochelydidae), from northern Australia." Canadian Journal of Zoology 78, no. 3 (2000): 373–92. http://dx.doi.org/10.1139/z99-214.

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Standard series of embryonic stages are the primary basis for organising information in embryological studies and for ageing eggs and embryos in field studies. In this paper we calibrate the developmental series for the pig-nosed turtle, Carettochelys insculpta, from northern Australia against an established series for Chelydra serpentina, carefully noting unique attributes of C. insculpta. We also extend existing non-destructive approaches to staging embryos by identifying several additional specific embryological attributes visible externally or by candling. A chronological sequence of attri

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10

Doody, J. Sean, Arthur Georges, Jeanne E. Young, et al. "Embryonic aestivation and emergence behaviour in the pig-nosed turtle, Carettochelys insculpta." Canadian Journal of Zoology 79, no. 6 (2001): 1062–72. http://dx.doi.org/10.1139/cjz-79-6-1062.

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11

Davenport, John, Julia Davenport, Cheong-Hoong Diong, and K. H. Low. "Swimming and bipedal bottom-running in the pig-nosed turtle Carettochelys insculpta Ramsay, 1886." Journal of Natural History 50, no. 33-34 (2016): 2097–105. http://dx.doi.org/10.1080/00222933.2016.1180720.

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12

Young, Jeanne E., Arthur Georges, J. Sean Doody, Peter B. West, and Rachael L. Alderman. "Pivotal range and thermosensitive period of the pig-nosed turtle, Carettochelys insculpta (Testudines: Carettochelydidae), from northern Australia." Canadian Journal of Zoology 82, no. 8 (2004): 1251–57. http://dx.doi.org/10.1139/z04-105.

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Understanding temperature-dependent sex determination in nature often depends on knowledge of species-specific attributes that are integrated into the relationship between temperature and sex. We determined two such attributes for the pig-nosed turtle, Carettochelys insculpta Ramsay, 1886, in tropical Australia: the pivotal range in temperature that separates the male-producing domain from the female-producing domain, and the thermosensitive period during which the embryonic sex is influenced by temperature. The pivotal range for C. insculpta was very narrow, spanning only about 1 °C, and was

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13

Doody, J. Sean, John Roe, Phillip Mayes, and Lesley Ishiyama. "Telemetry tagging methods for some freshwater reptiles." Marine and Freshwater Research 60, no. 4 (2009): 293. http://dx.doi.org/10.1071/mf08158.

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Reptiles are often ignored or under-studied in freshwater systems. An understanding of their biology and thus their role in aquatic communities can be greatly advanced by studies using radio telemetry. In turn, the value of radio telemetry for research depends on the availability of suitable and reliable methods of attaching or implanting radio transmitters. The present study describes transmitter attachment and implantation techniques for selected freshwater reptiles, including the eastern and northern long-necked turtles (Chelodina longicollis and Chelodina rugosa, respectively), the pig-nos

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14

Rivera, A. R. V., G. Rivera, and R. W. Blob. "Forelimb kinematics during swimming in the pig-nosed turtle, Carettochelys insculpta, compared with other turtle taxa: rowing versus flapping, convergence versus intermediacy." Journal of Experimental Biology 216, no. 4 (2012): 668–80. http://dx.doi.org/10.1242/jeb.079715.

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15

Eisemberg, C. C., M. Rose, B. Yaru, Y. Amepou, and A. Georges. "Salinity of the coastal nesting environment and its association with body size in the estuarine pig-nosed turtle." Journal of Zoology 295, no. 1 (2014): 65–74. http://dx.doi.org/10.1111/jzo.12179.

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16

Tkach, Vasyl V., and Scott D. Snyder. "Doodytrema carettochelydis n. gen., n. sp., (Digenea: Microscaphidiidae) from the Pig-Nosed Turtle, Carettochelys insculpta, (Cryptodira: Carettochelydidae) in Australia." Comparative Parasitology 73, no. 2 (2006): 165–71. http://dx.doi.org/10.1654/4238.1.

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17

Doody, J. Sean, Arthur Georges, and Jeanne E. Young. "Twice every second year: reproduction in the pig-nosed turtle, Carettochelys insculpta, in the wet–dry tropics of Australia." Journal of Zoology 259, no. 2 (2003): 179–88. http://dx.doi.org/10.1017/s0952836902003217.

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18

Beggs, Kerry, Jeanne Young, Arthur Georges, and Peter West. "Ageing the eggs and embryos of the pig-nosed turtle, Carettochelys insculpta (Chelonia: Carettochelydidae), from northern Australia." Canadian Journal of Zoology 78, no. 3 (2000): 373–92. http://dx.doi.org/10.1139/cjz-78-3-373.

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19

Doody, J. S., J. E. Young, and A. Georges. "Sex Differences in Activity and Movements in the Pig-Nosed Turtle, Carettochelys insculpta, in the Wet-Dry Tropics of Australia." Copeia 2002, no. 1 (2002): 93–103. http://dx.doi.org/10.1643/0045-8511(2002)002[0093:sdiaam]2.0.co;2.

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20

Georges, A. "Thermal-Characteristics and Sex Determination in Field Nests of the Pig-Nosed Turtle, Carettochelys-Insculpta (Chelonia, Carettochelydidae), From Northern Australia." Australian Journal of Zoology 40, no. 5 (1992): 511. http://dx.doi.org/10.1071/zo9920511.

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Carettochelys insculpta lays its eggs in shallow nests constructed in clean fine sand adjacent to water. Six nests had the following thermal characteristics: (1) core temperatures ranging from 26.1 to 33.7-degrees-C early in September, from 30.0 to 38.7-degrees-C early in October and from 28.4 to 36.8-degrees-C early in November; (2) a pronounced daily cycle in core temperatures of up to 6.4-degrees-C in amplitude, with the minimum occurring after sunrise in mid-morning and the maximum occurring in the evening; (3) a difference in the temperatures experienced by the top and bottom eggs in a si

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21

Eisemberg, Carla C., Mark Rose, Benedict Yaru, and Arthur Georges. "Demonstrating decline of an iconic species under sustained indigenous harvest – The pig-nosed turtle (Carettochelys insculpta) in Papua New Guinea." Biological Conservation 144, no. 9 (2011): 2282–88. http://dx.doi.org/10.1016/j.biocon.2011.06.005.

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22

Adrian, Brent, Patricia A. Holroyd, J. Howard Hutchison, and KE Beth Townsend. "Additional records and stratigraphic distribution of the middle Eocene carettochelyid turtle Anosteira pulchra from the Uinta Formation of Utah, North America." PeerJ 8 (August 24, 2020): e9775. http://dx.doi.org/10.7717/peerj.9775.

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Background Anosteira pulchra is one of two species of the obligately-aquatic freshwater clade Carettochelyidae (pig-nosed turtles) from the Eocene of North America. Anosteira pulchra is typically rare in collections, and their distribution is poorly documented. The Uinta Formation [Fm.] contains a diverse assemblage of turtles from the Uintan North American Land Mammal Age. Whereas turtles are abundantly preserved in the Uinta Fm., A. pulchra has been reported only from a few specimens in the Uinta C Member. Methods We describe new records of Anosteira pulchra from the Uinta Basin and analyze

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23

Eisemberg, Carla C., Yolarnie Amepou, Mark Rose, Benedict Yaru, and Arthur Georges. "Defining priority areas through social and biological data for the pig-nosed turtle (Carettochelys insculpta) conservation program in the Kikori Region, Papua New Guinea." Journal for Nature Conservation 28 (November 2015): 19–25. http://dx.doi.org/10.1016/j.jnc.2015.08.003.

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24

Doody, J. Sean, Peter West, and Arthur Georges. "Beach Selection in Nesting Pig-Nosed Turtles, Carettochelys insculpta." Journal of Herpetology 37, no. 1 (2003): 178–82. http://dx.doi.org/10.1670/0022-1511(2003)037[0178:bsinpn]2.0.co;2.

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25

Shepherd, Chris R., Lalita Gomez, and Vincent Nijman. "Illegal wildlife trade, seizures and prosecutions: A 7.5-year analysis of trade in pig-nosed turtles Carettochelys insculpta in and from Indonesia." Global Ecology and Conservation 24 (December 2020): e01249. http://dx.doi.org/10.1016/j.gecco.2020.e01249.

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