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Auteur : Grafiati
Publié le 11 mars 2023

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1

Aceto, M., C. Sarzanini, O. Abollino, G. Sacchero et E. Mentasti. « Distribution of Minor and Trace Metals in Carezza Lake (ANTARCTICA) Ecosystem ». International Journal of Environmental Analytical Chemistry 55, no 1-4 (juillet 1994) : 165–77. http://dx.doi.org/10.1080/03067319408026215.

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Charlotte Ross. « ‘La carezza incompiuta’ : Queer Aesthetics, Desire, and Censorship in Ticchioni's Il suicidio di un esteta ». Modern Language Review 111, no 2 (2016) : 390. http://dx.doi.org/10.5699/modelangrevi.111.2.0390.

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3

ABOLLINO, ORNELLA, MAURIZIO ACETO, SANDRO BUOSO, MASSIMO GASPARON, WILLIAM J. GREEN, MERY MALANDRINO et EDOARDO MENTASTI. « Distribution of major, minor and trace elements in lake environments of Antarctica ». Antarctic Science 16, no 3 (septembre 2004) : 277–91. http://dx.doi.org/10.1017/s0954102004002111.

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The concentrations of major, minor and trace metals were measured in water samples collected from five shallow Antarctic lakes (Carezza, Edmonson Point (No 14 and 15a), Inexpressible Island and Tarn Flat) found in Terra Nova Bay (northern Victoria Land, Antarctica) during the Italian Expeditions of 1993-2001. The total concentrations of a large suite of elements (Al, As, Ba, Ca, Cd, Ce, Co, Cr, Cs, Cu, Fe, Ga, Gd, K, La, Li, Mg, Mn, Mo, Na, Nd, Ni, Pb, Pr, Rb, Sc, Si, Sr, Ta, Ti, U, V, Y, W, Zn and Zr) were determined using spectroscopic techniques (ICP-AES, GF-AAS and ICP-MS). The results are similar to those obtained for the freshwater lakes of the Larsemann Hills, East Antarctica, and for the McMurdo Dry Valleys. Principal Component Analysis (PCA) and Cluster Analysis (CA) were performed to identify groups of samples with similar characteristics and to find correlations between the variables. The variability observed within the water samples is closely connected to the sea spray input; hence, it is primarily a consequence of geographical and meteorological factors, such as distance from the ocean and time of year. The trace element levels, in particular those of heavy metals, are very low, suggesting an origin from natural sources rather than from anthropogenic contamination.
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Wiles, M., et TG Rand. « Integumental ulcerative disease in a loggerhead turtle Carella caretta -. the Bermuda Aquarium : microbiology and histopathology ». Diseases of Aquatic Organisms 3 (1987) : 85–90. http://dx.doi.org/10.3354/dao003085.

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Gastaldi, Roberto, Paola Borgia et Mohamad Maghnie. « Lo iodio nell’alimentazione dell’età evolutiva ». L'Endocrinologo 22, no 4 (août 2021) : 293–97. http://dx.doi.org/10.1007/s40619-021-00924-2.

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SommarioLo iodio viene assunto esclusivamente attraverso gli alimenti e rappresenta un componente essenziale per la sintesi degli ormoni tiroidei. Una carenza iodica misconosciuta da inadeguato apporto dietetico che si instaura nei primi anni di vita può essere responsabile di scarsa crescita e disordini dello sviluppo neuro-cognitivo. Negli ultimi anni è aumentata la prevalenza delle allergie alimentari e dei cultori di diete vegane nei paesi occidentali. Entrambe le situazioni impongono restrizioni dietetiche, limitando le fonti di importanti nutrienti come iodio, ferro, zinco, vitamina D, calcio e vitamina B12. Nelle allergie alimentari e in regime dietetico vegano, infatti, i primi alimenti ad essere esclusi sono proprio quelli a maggior contenuto di iodio, come pesce, latte, uova e derivati. L’apporto di iodio può dunque divenire insufficiente qualora non ci sia adeguato utilizzo di fonti di iodio alternative, come il sale iodato. Pertanto, risulta fondamentale che gli operatori sanitari siano a conoscenza dei possibili rischi di carenze nutrizionali in bambini con allergia alimentare, vegani o entrambi, al fine di garantire un attento monitoraggio auxologico e nutrizionale e soddisfare il fabbisogno energetico e nutritivo. In questo articolo riassumiamo i principali aspetti riguardanti l’apporto iodico in dieta vegana e nelle diete di esclusione dei bambini con allergie alimentari, revisionando la letteratura su questi argomenti e fornendo alcuni suggerimenti per i pediatri.
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6

Jeansonne, James H., Thomas Moore, David Bernhart et Melissa Snover. « CONDUCTING A NATURAL RESOURCE DAMAGE ASSESSMENT (NRDA) FOR SEA TURTLE INJURY RESULTING FROM AN OIL SPILL NEAR FORT LAUDERDALE, FL ». International Oil Spill Conference Proceedings 2005, no 1 (1 mai 2005) : 95–99. http://dx.doi.org/10.7901/2169-3358-2005-1-95.

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ABSTRACT Following a mystery oil spill near Ft. Lauderdale, Florida in August 2000, natural resource trustee agencies (Trustees) conducted a natural resource damage assessment (NRDA) under the Oil Pollution Act of 1990 (OPA). During the NRDA, injury to several life stages of Loggerhead sea turtles (Carena caretta) and Green sea turtles (Chelonia my das) was quantified using a computer model, SIMAP (French-McCay, 2001), and the type and scale of restoration required was determined. Quantification of injury required Trustees to determine key model input parameters based on a variety of scientific data sources. The restoration scaling portion of this NRDA required Trustees to quantify the number of Loggerhead sea turtle hatchlings it would take to replace a post-pelagic juvenile (age 17 to 20 years) and an adult female (42 to 50 years old). To accomplish this, Trustees developed a simple model based on recent life stage and population dynamics assumptions for the south Florida Loggerhead sub-population. Details of the sea turtle NRDA method and rationale for determining the required model input parameters are discussed.
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7

Rutledge, Felix N. « Luigi Carenza (1926–1992) ». Gynecologic Oncology 46, no 3 (septembre 1992) : 271–72. http://dx.doi.org/10.1016/0090-8258(92)90214-4.

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8

Vilaça, Sibelle Torres, et Fabricio Rodrigues dos Santos. « Molecular Data for the Sea Turtle Population in Brazil ». Dataset Papers in Science 2013 (22 août 2013) : 1–7. http://dx.doi.org/10.1155/2013/196492.

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We report here a dataset comprising nine nuclear markers for the Brazilian population of Cheloniidae turtles: hawksbills (Eretmochelys imbricata), loggerheads (Caretta caretta), olive ridleys (Lepidochelys olivacea), and green turtles (Chelonia mydas). Because hybridization is a common phenomenon between the four Cheloniidae species nesting on the Brazilian coast, we also report molecular markers for the hybrids E. imbricata × C. caretta, C. caretta × L. olivacea, and E. imbricata × L. olivacea and for one hybrid E. imbricata × C. mydas and one between three species C. mydas × E. imbricata × C. caretta. The data was used in previous studies concerning (1) the description of frequent hybrids C. caretta × E. imbricata in Brazil, (2) the report of introgression in some of these hybrids, and (3) population genetics. As a next step for the study of these hybrids and their evolution, genome-wide studies will be performed in the Brazilian population of E. imbricata, C. caretta, and their hybrids.
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9

Báez, José C., Juan A. Camiñas, Julio Valeiras, Francisco Conde et Antonio Flores-Moya. « First record of the epizoic red seaweed Polysiphonia carettia Hollenberg in the Mediterranean Sea. » Acta Botanica Malacitana 26 (1 décembre 2001) : 197–201. http://dx.doi.org/10.24310/abm.v26i0.7417.

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Primera cita del alga roja epizoica Polysiphonia carettia Hollenberg en el mar Mediterráneo Key words. Caretta caretta, epibionts, Mediterranean Sea, Polysiphonia carettia. Palabras claves. Caretta carom, cpibiontes, Mar Mediterráneo, Polysiphonia carettia.
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10

Zanon, Tobia. « «Carezze» italiane di Paul Valéry ». Italica Belgradensia 2019, Speciale (2019) : 117–25. http://dx.doi.org/10.18485/italbg.2019.ns_zogovic.9.

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11

Gyuris, E., et CJ Limpus. « The Loggerhead Turtle, Caretta-Caretta, in Queensland - Population Breeding Structure ». Wildlife Research 15, no 2 (1988) : 197. http://dx.doi.org/10.1071/wr9880197.

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Population models proposed as a result of independent tagging programs of nesting Caretta caretta in Queensland are in disagreement about the size of discrete breeding units. An electrophoretic survey was conducted to assess the relevance of genetic variation as revealed by electrophoresis to the investigation of Caretta caretta population breeding structure. Low level electrophoretic variability (H*L(obs) = 0.016) was found. The geographical distribution of alleles, when compared with tag-recapture data and other aspects of life history, indicated that discrete breeding populations of C. caretta in Queensland are larger than previously thought. C. caretta nesting on the mainland beaches and on the cays of the Capricornia Section of the Great Barrier Reef Marine Park form a panmictic population. The data indicate that those nesting on the Swain Reefs cays do not interbreed with the mainland-Capricornia breeding population.
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12

Hays, Graeme C., et John R. Speakman. « Nest placement by loggerhead turtles, Caretta caretta ». Animal Behaviour 45, no 1 (janvier 1993) : 47–53. http://dx.doi.org/10.1006/anbe.1993.1006.

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13

Upton, Steve J., Daniel K. Odell et Michael T. Walsh. « Eimeria caretta sp.nov. (Apicomplexa : Eimeriidae) from the loggerhead sea turtle, Caretta caretta (Testudines) ». Canadian Journal of Zoology 68, no 6 (1 juin 1990) : 1268–69. http://dx.doi.org/10.1139/z90-189.

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Eimeria caretta sp.nov. (Apicomplexa: Eimeriidae) is described from the feces of a stranded loggerhead turtle, Caretta caretta (Testudines), rescued from the Atlantic coast near Jensen Beach, Hutchinson Island, Martin County, Florida. Oocysts are subspherical to ellipsoidal, 24.5 × 22.0 (21.4–28.0 × 18.4–24.0) μm, with a smooth, bilayered wall. Micropyle, polar granule, and oocyst residuum are absent. Sporocysts are ovoid, 14.3 × 8.9(12.8–16.0 × 8.2–10.0) μm, and possess a Stieda body but no substieda body. The Stieda body is unusual in that 12–20 long, thin filaments project from its surface. Sporozoites are elongate, each with two refractile bodies. The sporocyst residuum consists only of scattered granules. This coccidian is most similar to Eimeria filamentifera Wacha and Christiansen 1979 from the common snapping turtle, Chelydra serpentina, but differs because it possesses more numerous and elongate filaments associated with the Stieda body and lacks an oocyst residuum.
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14

Zinenko, O., K. A. Vishnyakova, L. Stoyanov et P. E. Gol’din. « Record of the Loggerhead Sea Turtle, Caretta caretta (Testudines, Cheloniidae), in the Black Sea with the Review of the Species Occurrence in the Region ». Zoodiversity 55, no 2 (2021) : 127–32. http://dx.doi.org/10.15407/zoo2021.02.127.

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A rare live record of the loggerhead sea turtle Caretta caretta (Linnaeus, 1758) is reported from the Dzharylgach Gulf in the north-western Black Sea. This is the first record from Ukrainian waters since 1962 and the northernmost record of the species in the Black Sea. The loggerhead sea turtles of the east Mediterranean origin are increasingly often seen in the Marmara and the Black Sea during the latest decade, which is an evidence for potential expansion of this species range, at least partly due to climate changes. Key words: sea turtles, Caretta caretta, Black Sea, Ukraine, range expansion.
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15

Tomen, Bihter. « Pembe Caretta ». Journal of Middle East Women's Studies 14, no 2 (1 juillet 2018) : 255–58. http://dx.doi.org/10.1215/15525864-6680400.

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16

MacLean, Robert A., Craig A. Harms et Joanne Braun-McNeill. « PROPOFOL ANESTHESIA IN LOGGERHEAD (CARETTA CARETTA) SEA TURTLES ». Journal of Wildlife Diseases 44, no 1 (janvier 2008) : 143–50. http://dx.doi.org/10.7589/0090-3558-44.1.143.

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17

Nutter, F. B., D. D. Lee, M. A. Stamper, G. A. Lewbart et M. K. Stoskopf. « Hemiovanosalpingecomy in a loggerhead sea turtle (Caretta caretta) ». Veterinary Record 146, no 3 (15 janvier 2000) : 78–80. http://dx.doi.org/10.1136/vr.146.3.78.

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18

Hays, G. C., et J. R. Speakman. « Clutch size for Mediterranean loggerhead turtles (Caretta caretta) ». Journal of Zoology 226, no 2 (février 1992) : 321–27. http://dx.doi.org/10.1111/j.1469-7998.1992.tb03842.x.

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19

Coles, William C., John A. Musick et Lindsay A. Williamson. « Skeletochronology Validation from an Adult Loggerhead (Caretta caretta) ». Copeia 2001, no 1 (février 2001) : 240–42. http://dx.doi.org/10.1643/0045-8511(2001)001[0240:svfaal]2.0.co;2.

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20

Harry, J. L., et D. A. Briscoe. « Multiple Paternity in the Loggerhead Turtle (Caretta caretta) ». Journal of Heredity 79, no 2 (mars 1988) : 96–99. http://dx.doi.org/10.1093/oxfordjournals.jhered.a110480.

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BOWEN, BRIAN W., ANNA L. BASS, SHAIO-MEI CHOW, MEREDITH BOSTROM, KAREN A. BJORNDAL, ALAN B. BOLTEN, TOSHINORI OKUYAMA et al. « Natal homing in juvenile loggerhead turtles (Caretta caretta) ». Molecular Ecology 13, no 12 (21 octobre 2004) : 3797–808. http://dx.doi.org/10.1111/j.1365-294x.2004.02356.x.

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22

Türkozan, Oğuz, Çetin Ilgaz et Serdar Sak. « Carapacial scute variation in Loggerhead Turtles,Caretta caretta ». Zoology in the Middle East 24, no 1 (janvier 2001) : 137–42. http://dx.doi.org/10.1080/09397140.2001.10637893.

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23

Reich, Kimberly J., Karen A. Bjorndal, Michael G. Frick, Blair E. Witherington, Chris Johnson et Alan B. Bolten. « Polymodal foraging in adult female loggerheads (Caretta caretta) ». Marine Biology 157, no 1 (25 septembre 2009) : 113–21. http://dx.doi.org/10.1007/s00227-009-1300-4.

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Valente, A. L., M. L. Parga, Y. Espada, S. Lavin, F. Alegre, I. Marco et R. Cuenca. « Ultrasonographic imaging of loggerhead sea turtles (Caretta caretta) ». Veterinary Record 161, no 7 (18 août 2007) : 226–32. http://dx.doi.org/10.1136/vr.161.7.226.

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Crespo-Picazo, J. L., D. García-Párraga, F. L. García-Peña, N. Frías, J. M. Corpa et J. Ortega. « Perinatal Mortality in the Loggerhead Turtle (Caretta caretta) ». Journal of Comparative Pathology 156, no 1 (janvier 2017) : 79. http://dx.doi.org/10.1016/j.jcpa.2016.11.077.

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26

Houghton, J. D. R., et G. C. Hays. « Asynchronous emergence by loggerhead turtle ( Caretta caretta ) hatchlings ». Naturwissenschaften 88, no 3 (27 avril 2001) : 133–36. http://dx.doi.org/10.1007/s001140100212.

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Minisola, Salvatore. « La carenza di vitamina D nell’adulto ». L'Endocrinologo 6, no 1 (mars 2005) : 3–7. http://dx.doi.org/10.1007/bf03344506.

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28

De Majo, M., F. Macri, M. Masucci, G. Coci et MG Pennisi. « Clinical ultrasonography in loggerhead sea turtles (Caretta caretta) : imaging of pathological features ». Veterinární Medicína 61, No. 3 (15 juillet 2016) : 155–61. http://dx.doi.org/10.17221/8767-vetmed.

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29

Lohmann, K. J. « Magnetic orientation by hatchling loggerhead sea turtles (Caretta caretta) ». Journal of Experimental Biology 155, no 1 (1 janvier 1991) : 37–49. http://dx.doi.org/10.1242/jeb.155.1.37.

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Laboratory experiments were conducted to test the ability of loggerhead sea turtle hatchlings (Caretta caretta L.) to orient using the magnetic field of the earth. Hatchlings were tethered to a rotatable lever-arm apparatus which tracked swimming orientation in complete darkness. Hatchlings tested in the earth's magnetic field were nonrandomly oriented with a mean angle of 42 degrees; those tested under an earth-strength field with a reversed horizontal component were also nonrandomly oriented, but with a mean angle of 196 degrees. The distributions under the two magnetic field conditions were significantly different, indicating that loggerhead sea turtle hatchlings can detect the magnetic field of the earth and use it as a cue in orientation.
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LUTCAVAGE, M. E., P. L. LUTZ et H. BAIER. « Gas Exchange in the Loggerhead Sea Turtle Caretta Caretta ». Journal of Experimental Biology 131, no 1 (1 septembre 1987) : 365–72. http://dx.doi.org/10.1242/jeb.131.1.365.

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Pulmonary CO diffusion capacity (DLCO), lung volume (VL), oxygen uptake (Vo2) and pulmonary blood flow (QL) were measured simultaneously in the loggerhead sea turtle Caretta caretta (Linnaeus) (8–11 kg) using a gas rebreathing technique (syringe pump ventilation). Calculated DLCO and Vo2 values in the loggerhead turtle are approximately twice those of non-varanid reptiles and about 25 % of values for resting mammals. Evidence based on an estimated lung-capillary O2 gradient, δPo2, shows that only a small driving gradient is required for O2 conductance across the loggerhead turtle lung. Pulmonary blood flow values are high compared to those for other reptiles; on the basis of the Fick principle, this implies a substantial blood convection requirement. Differences in oxygen transport mechanisms between the loggerhead sea turtle and other highly aerobic but terrestrial reptiles may result from divergent lung structures and breathing patterns. In sea turtles, the coupling of respiration with locomotory behaviour is one factor that may limit aerobic performance. Since sea turtles have only intermittent access to air, they are required to load both arterial and venous blood with O2 before submerging
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Manire, Charles A., Michael J. Kinsel, Eric T. Anderson, Tonya M. Clauss et Lynne Byrd. « Lungworm Infection in Three Loggerhead Sea Turtles, Caretta caretta ». Journal of Zoo and Wildlife Medicine 39, no 1 (mars 2008) : 92–98. http://dx.doi.org/10.1638/2007-0092.1.

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RAIDAL, SR, PL SHEARER et RIT PRINCE. « Chronic shoulder osteoarthritis in a loggerhead turtle (Caretta caretta) ». Australian Veterinary Journal 84, no 7 (juillet 2006) : 231–34. http://dx.doi.org/10.1111/j.1751-0813.2006.00003.x.

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Reckendorf, Anja, Kathryn Tuxbury, Julie Cavin, Gena Silver, Jennifer Brisson, Claire McManus, Brian Stacy, Constance Merigo et Charles Innis. « Laryngeal Paralysis in a Loggerhead Sea Turtle (Caretta caretta) ». Journal of Herpetological Medicine and Surgery 26, no 1-2 (1 mars 2016) : 20. http://dx.doi.org/10.5818/1529-9651-26.1-2.20.

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SHAMBLIN, BRIAN M., BRANT C. FAIRCLOTH, MARK DODD, ALICIA WOOD-JONES, STEVEN B. CASTLEBERRY, JOHN P. CARROLL et C. JOSEPH NAIRN. « Tetranucleotide microsatellites from the loggerhead sea turtle (Caretta caretta) ». Molecular Ecology Notes 7, no 5 (septembre 2007) : 784–87. http://dx.doi.org/10.1111/j.1471-8286.2007.01701.x.

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Day, Rusty D., Steven J. Christopher, Paul R. Becker et David W. Whitaker. « Monitoring Mercury in the Loggerhead Sea Turtle,Caretta caretta ». Environmental Science & ; Technology 39, no 2 (janvier 2005) : 437–46. http://dx.doi.org/10.1021/es049628q.

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Kitsos, Miltiadis-Spyridon, Magdalini Christodoulou, Christos Arvanitidis, Michalis Mavidis, Ioannis Kirmitzoglou et Athanasios Koukouras. « Composition of the organismic assemblage associated with Caretta caretta ». Journal of the Marine Biological Association of the United Kingdom 85, no 2 (31 mars 2005) : 257–61. http://dx.doi.org/10.1017/s0025315405011136h.

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The organismic assemblage associated with Caretta caretta was studied in 37 loggerhead turtles, washed ashore dead at various localities in the northern Aegean Sea. A total number of 63 macrobenthic species and 17 species of macroalgae were identified. From these species, 41 and 13 respectively are reported for the first time as epibionts of this turtle. Analysis of the epibiont species distribution on six loggerhead turtles gave some evidence regarding the settlement preferences of certain epibiont species. From a biogeographical point of view, 61·3% of the epibiont species were cosmopolitan, 30·7% had an Atlanto-Mediterranean distribution, while 8% were Mediterranean endemics.
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Pike, David A. « Environmental correlates of nesting in loggerhead turtles, Caretta caretta ». Animal Behaviour 76, no 3 (septembre 2008) : 603–10. http://dx.doi.org/10.1016/j.anbehav.2008.04.010.

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Lutcavage, M. E., P. L. Lutz et H. Baier. « Respiratory mechanics of the loggerhead sea turtle, Caretta caretta ». Respiration Physiology 76, no 1 (avril 1989) : 13–24. http://dx.doi.org/10.1016/0034-5687(89)90014-5.

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Young, Morgan, Michael Salmon et Richard Forward. « Visual Wavelength Discrimination by the Loggerhead Turtle, Caretta caretta ». Biological Bulletin 222, no 1 (février 2012) : 46–55. http://dx.doi.org/10.1086/bblv222n1p46.

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40

Jacobson, ER, BL Homer, BA Stacy, EC Greiner, NJ Szabo, CL Chrisman, F. Origgi et al. « Neurological disease in wild loggerhead sea turtles Caretta caretta ». Diseases of Aquatic Organisms 70 (2006) : 139–54. http://dx.doi.org/10.3354/dao070139.

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41

Frick, MG, KL Williams, AB Bolten, KA Bjorndal et HR Martins. « Foraging ecology of oceanic-stage loggerhead turtles Caretta caretta ». Endangered Species Research 9 (14 décembre 2009) : 91–97. http://dx.doi.org/10.3354/esr00227.

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42

Manire, Charles A., Lynne Byrd, Corie L. Therrien et Kelly Martin. « Mating-induced ovulation in loggerhead sea turtles,Caretta caretta ». Zoo Biology 27, no 3 (2008) : 213–25. http://dx.doi.org/10.1002/zoo.20171.

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Cutrim, Caio Henrique Gonçalves, et Vinícius Albano Araújo. « Sea turtle strandings and the importance of the restinga de Jurubatiba National Park in loggerhead (Caretta caretta) nesting sites ». Nature and Conservation 14, no 4 (1 janvier 2022) : 34–46. http://dx.doi.org/10.6008/cbpc2318-2881.2021.004.0004.

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Protected areas represent important refuges for several species of fauna, mitigating human impacts and providing food resources and reproductive sites. In this study, analyzed the stranding pattern of sea turtles and the importance of the largest restinga protected area in Brazil, the Restinga de Jurubatiba National Park, Rio de Janeiro, Brazil, as a potential nesting site for Caretta caretta. A total of 352 strandings were recorded from October 2017 to September 2020 by direct monitoring on the beaches. The species with the highest recorded stranding was Chelonia mydas (n = 146), followed by Lepidochelys olivacea (n = 100), Caretta caretta (n = 91), Dermochelys coriacea (n = 11) and Eretmochelys imbricata (n = 4). The highest number of stranding records occurred in the end of winter and during spring. A total of 223 nests were registered, mostly in spring and summer, with most records of C. caretta nesting between November and December. The occurrence of nesting in the park area demonstrates it is importance for the conservation of sea turtles, since the lack of urbanization reduces anthropogenic impacts such as overfishing, egg collection, running over and artificial lighting, which favors that these animals complete their cycle of life.
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44

Careaga, Gloria, Pedro Paulo Gomes Pereira et Wilza Vieira Villela. « Género y sexualidad en México : entrevista con Gloria Careaga ». Ciência & ; Saúde Coletiva 24, no 4 (avril 2019) : 1427–30. http://dx.doi.org/10.1590/1413-81232018244.15122017.

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Resumen En esta entrevista con Gloria Careaga, una de las principales investigadoras en género y sexualidad en México, exploramos las relaciones entre género y sexualidad en su país. Además, hemos examinado las contribuciones de Careaga al campo de la salud pública.
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45

Barrios, César Augusto, Moises Fernandes Bezerra et Luiz Drude Lacerda. « USO DE FRAGMENTOS DE CARAPAÇA PARA MONITORAMENTO DO MERCÚRIO EM DUAS ESPÉCIES DE TARTARUGAS MARINHAS NO NORDESTE DO BRASIL ». Arquivos de Ciências do Mar 51, no 1 (11 septembre 2018) : 93. http://dx.doi.org/10.32360/acmar.v51i1.32973.

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Este trabalho compara concentrações de Hg para duas espécies de tartarugas marinhas, Caretta caretta e Chelonia mydas, encontradas na zona costeira do nordeste brasileiro e fazendo uso de fragmentos de carapaça como método não invasivo de monitoramento dos níveis ambientais de Hg. Os resultados não mostraram diferença significativa entre as concentrações de Hg nas duas espécies. Porém, a comparação entre a C. caretta (adultos) e C. mydas (juvenis e subadulto), permitiu observar que a dieta exerce influência na concentração de Hg nesses organismos. Tornando relevante, em futuros estudos, a quantificação de Hg tanto nas espécies em estudo quanto em sua fonte alimentar.
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46

Koo, Kyo-Soung, Sang-Hyun Han et Hong-Shik Oh. « First Report of a Hybridization between Caretta caretta and Chelonia mydas from Jeju Island, South Korea ». Korean Journal of Environmental Biology 32, no 4 (30 décembre 2014) : 377–81. http://dx.doi.org/10.11626/kjeb.2014.32.4.377.

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47

Avşar, Dursu, Sinan Mavruk, Hacer Yeldan, Meltem Manaşırlı et Caner Enver Özyurt. « TEMPORAL CHANGES OF THE NESTING TRACKS TO THE SEA TURTLES (Caretta caretta and Chelonia mydas) ON THE SUGÖZÜ BEACH ». e-Journal of New World Sciences Academy 13, no 1 (23 janvier 2018) : 62–73. http://dx.doi.org/10.12739/nwsa.2018.13.1.5a0095.

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48

Limpus, CJRPC. « The Loggerhead Turtle, Caretta caretta, in Queensland : Observations on Internesting Behaviour ». Wildlife Research 12, no 3 (1985) : 535. http://dx.doi.org/10.1071/wr9850535.

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An internesting Caretta caretta remained associated with a single underwater refuge adjacent to her nesting beach throughout an entire breeding season. She maintained this association even when repeatedly disturbed by divers. The relevance of this behaviour to turtle mortality in trawling fisheries is discussed.
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49

Caracappa, S., A. Pisciotta, M. F. Persichetti, G. Caracappa, R. Alduina et M. Arculeo. « Nonmodal scutes patterns in the Loggerhead Sea Turtle (Caretta caretta) : a possible epigenetic effect ? » Canadian Journal of Zoology 94, no 5 (mai 2016) : 379–83. http://dx.doi.org/10.1139/cjz-2015-0248.

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Eleven specimens of the threatened Loggerhead Sea Turtle (Caretta caretta (L., 1758)) were caught accidentally by fishermen in different parts of Sicily (Mediterranean Sea). Five of them showed an atypical number of carapacial and plastron scutes, making the immediate identification of the specimens as C. caretta difficult. Both genetic and epigenetic analysis were carried out on these specimens. Sequencing of a 649 bp sequence of the mitochondrial cytochrome c oxidase I (COI) gene allowed us to classify all the individuals as C. caretta. Epigenetic analysis, performed by evaluating the total level of DNA cytosine methylation, showed a reduced and significant (F = 72.65, p < 0.01) global level of methylated cytosines in the turtles with nonmodal scutes compared with the normal turtles. Our results suggest that the variability in the number of scutes could be dependent on the environmental conditions during embryonic incubation, via an epigenetic mechanism. This finding could have implications in our understanding of the pathways of morphological evolution and diversification in the chelonians.
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Corsini-Foka, Maria, Gerasimos Kondylatos et Elias Santorinios. « Increase of sea turtles stranding records in Rhodes Island (eastern Mediterranean Sea) : update of a long-term survey ». Journal of the Marine Biological Association of the United Kingdom 93, no 7 (29 mai 2013) : 1991–2002. http://dx.doi.org/10.1017/s0025315413000556.

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A total of 209 strandings of sea turtles (152 loggerhead turtles Caretta caretta, 42 green turtles Chelonia mydas, 15 unidentified) were recorded during the period 1984–2011 along the coasts of Rhodes (Aegean Sea, Greece). The proportion of dead to live individuals was different in the two species. Stranded Caretta caretta were larger than Chelonia mydas. The size range of stranded green turtles, usually juveniles, appeared to increase since 2000, including the largest specimens ever observed in Greek waters. For both species, a tendency to strand more frequently on the west coast of the island, along fishing ground areas, was noted. The higher incidence of loggerhead turtle strandings was observed in summer, while more green turtle strandings were documented in winter. Factors involved in the increased trend of stranding records of both species, along with the acceleration of this phenomenon in the last decade, are discussed. Data from Rhodes provide evidence that human activities detrimentally affect mainly larger-sized loggerhead turtles living in shallow waters.
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