Nest temperature and respiratory gases during natural incubation in the broad-shelled river turtle, Chelodina expansa (Testudinata : Chelidae)

Temperature was monitored in three natural nests, and oxygen and carbon dioxide partial pressure monitored in one natural nest of the broad-shelled river turtle, Chelodina expansa, throughout incubation. Nest temperature decreased after nest construction in autumn, remained low during winter and gradually increased in spring to a maximum in summer. In a nest where temperature was recorded every hour, temperature typically fluctuated through a 2 degrees C cycle on a daily basis throughout the entire incubation period, and the nest always heated faster than it cooled. Oxygen and carbon dioxide partial pressures in this nest were similar to soil oxygen and carbon dioxide partial pressures for the first 5 months of incubation, but nest respiratory gas tensions deviated from the surrounding soil over the last three months of incubation. Nest respiratory gas tensions were not greatly different from those in the atmosphere above the ground except after periods of rain. After heavy rain during the last 3 months of incubation the nest became moderately hypoxic (P-O2 similar to 100 Torr) and hypercapnic (P-CO2 similar to 50 Torr) for several successive days. These short periods of hypoxia and hypercapnia were not lethal.

Patterns of lipid storage and mobilisation in the female green sea turtle (Chelonia mydas)

Reproductive data from southern Queensland indicate that vitellogenesis in female Chelonia mydas takes approximately 8 months and is followed by a migration to a breeding area. At Heron Island, females lay multiple clutches over approximately 3 months. To investigate how females mobilise and store lipid during the breeding season we collected plasma, yolk, and fat tissue samples from females at a variety of stages during the nesting season. In breeding females, concentrations of plasma triglyceride increased seasonally. They reached peak concentrations during vitellogenesis and courtship, remained high throughout the nesting season, and then declined to a nadir after the last clutch. Plasma protein concentration increased throughout the breeding season, peaking following the last clutch for the season. Yolk lipids were highest during courtship and were similar throughout the nesting season, suggesting that uptake of lipid by ovarian follicles is completed prior to the beginning of the nesting season. Plasma triglyceride decreases in females with prolonged periods of unsuccessful nesting, and total lipid levels in adipose tissue and follicle yolks were significantly lower in atretic females. It appears that: (1) endogenous energy reserves can be reduced by stochastic environmental events (such as those reducing nesting success), and (2) a metabolic shift signalling the end of the nesting season is characterised by a drop in plasma triglycerides and slight increase in total plasma protein.

Interactions among endocrinology, seasonal reproductive cycles and the nesting biology of the female green sea turtle

We collected data on plasma levels of testosterone+5a-dihydrotestosterone (T+DHT) and corticosterone (CORT) from adult female green sea turtles (Chelonia mydas) from southern Queensland during distinct stages of their reproductive cycle. Those females capable of breeding in a given year had elevated plasma steroid levels (T+DHT 0.91 +/- 0.08; CORT 1.05 +/- 0.29 ng/ml), associated with follicular development, until courtship began in October. At the beginning of the nesting season in November plasma levels of 2 CORT were related to when the female first nested (r(2) = 0.06; F = 10.45; P = 0.01). However, they were not correlated with the number of clutches a female laid in that season (F = 3.65; P = 0.08). We repeatedly sampled 23 turtles over the nesting season and profiled changes in steroids immediately following oviposition of each clutch. Levels of T+DHT (range 0.41-0.58 ng/ml) and CORT (range 2.13-2.81 ng/ml) were similar through the early stages of the nesting season and inter-nesting period, and declined to near basal levels (T+DHT 0.37 +/- 0.03 and CORT 1.85 +/- ng/ml) following the last clutch for the season. Steroid hormone levels were also low (T+DHT 0.38 +/- 0.16; CORT 0.46 +/- 0.21 ng/ml) in four independent post-breeding (atretic) females; samples for these females were taken at a time when body condition was presumably at the lowest for the season. Subtle changes in the nesting environment, such as variation in nesting habitat or the time of night that nesting occurred, were associated with a small and slow CORT increase. We suggest CORT is increased in nesting females to assist in lipid transfer to prepare the ovarian follicles and/or the reproductive organs for ovulation.

Influência das características geológicas do local de desova na duração da incubação e no sucesso da eclosão dos ovos de Caretta caretta na praia da Guanabara, Anchieta, Espírito Santo

O objetivo deste estudo foi analisar possíveis influências do local da desova no sucesso da eclosão e na duração da incubação de Caretta caretta (Linnaeus, 1758) no sul do estado do Espírito Santo. Geomorfologicamente a área da desova na praia da Guanabara, em Anchieta (ES), pode ser dividida em praia aberta e berma. Durante quatro estações reprodutivas foram coletados dados sobre o tamanho dos sedimentos, a altura dos ninhos em relação ao nível do mar, a compartimentação geomorfológica da praia, a data da desova, o número de filhotes vivos e o tamanho da ninhada. Os resultados mostraram variações dos principais parâmetros sedimentológicos entre os anos, indicando que as temporadas reprodutivas devem ser analisadas individualmente. O sucesso da eclosão não foi afetado pelas características geológicas do local da desova. A duração da incubação não variou entre a praia e a berma, apesar das diferenças significativas no tamanho do sedimento, na profundidade dos ninhos e na altura em relação ao nível do mar. A duração da incubação se correlacionou positivamente ao tamanho dos sedimentos, com ninhos em sedimentos mais grossos eclodindo mais cedo que os ninhos localizados em sedimentos mais finos. Como as características dos ninhos influenciam a duração da incubação, recomenda-se que a transferência de ninhos, quando inevitável, respeite as diferenças entre os locais de desova, principalmente, quanto à profundidade da câmara de ovos.

Características sedimentológicas de la Playa de Calheta de PAU (Isla de Boa Vista, República de Cabo Verde): implicaciones en la anidación de Caretta caretta (Linnaeus, 1758)

Programa de doctorado en Oceanografía

Desarrollo embrionario de Caretta caretta: análisis descriptivo de su evolución morfológica

Programa de Doctorado en Oceanografía

Estudio de los sonidos emitidos por las crías de tortuga boba, Caretta caretta, en el momento de la eclosión

Las crías Caretta caretta durante la eclosión y antes de salir del nido, emiten sonidos asociados a crujido y raspado del corion, así como chillidos, silbidos y tos, en un rango de frecuencia entre los 300 y 2600 Hz. No obstante, los silbidos y chillidos, que pueden ser asociables a un sistema de vocalización, se emiten a una frecuencia (1500-2600 Hz) mucho mayor al rango de sensibilidad descrito para esta especie (250-1000 Hz) y por tanto imperceptibles para ellas. Sin embargo, los sonidos producidos como consecuencia de ejercicios de respiración y expulsión de arena de las vías respiratorias, acompañados de tos (300-1200 Hz), por parte de las crías recién eclosionadas, son los únicos sonidos que podrían servir de señal y estimulación a la eclosión del resto de crías en el nido. ABSTRACT The hatchlings Caretta caretta, during the eclosion and before the abandon of their nest, produce sounds associated to creakling and scrape of the eggshell, and howl, whistle and cough, in a frequency range between 300 and 2600 Hz. Nevertheless, the howls and whistles, that could be associated to a vocalization apparatus, were emitted at a higher frequency (1500-2600 Hz) than the auditory range describe for this species (250-1000 Hz), and therefore probably inaudible for them. However, sounds generated as a consequence of breathing exercises and sand expulsion from the airways through coughs (300- 1200 Hz), by the recently hatched turtles, could be used as signal or stimulus for the hatch of the reminder eggs in the nest.

Estudio de la selección por el color del alimento en la tortuga boba Caretta caretta tras la eclosión

The behavior of newborn pups of loggerhead turtles (Caretta caretta) towards a potential food after hatching and before eating food for the first time was studied. There was no significant time trend approach and bite of potentially edible objects based on their color or size. However, a clear trend was observed for those objects that are transparent, white or red, independently the sex of the animal. Furthermore, it was verified that the turtles do not have a biting behavior to feed from first contact with water, but it comes after 3 or 4 days. There is also a learning process that determines the choice of targets of further attacks.

Biología reproductora de la tortuga boba (Caretta caretta Linneo, 1758) en la isla de Boavista, archipiélago de Cabo Verde

[ES]Este trabajo analiza diversos aspectos de la biología reproductora de la población nidificante de tortuga boba (Caretta caretta) en el archipiélago de Cabo Verde. Se estudiaron datos relacionados con la temporada de anidación, con la morfometría de las hembras, con el éxito de las salidas a tierra, con el tiempo de incubación y con el éxito de los nidos.

Voluntariado ambiental para la conservación de la Tortuga Boba (Caretta caretta) en la isla de Boa Vista

[ES]Cabo Verde Natura 2000 es una organización sin ánimo de lucro que en colaboración con ADS-Biodiversidad organiza, desde 1998, un voluntariado ambiental para la protección de la población de tortuga boba (Caretta caretta) de Cabo Verde. El 90 % de esta población nidifica en la isla de Boa Vista, donde la ONG tiene su centro de actuación. Cada temporada (de Junio a Octubre) acuden a los campamentos de Cabo Verde Natura 2000 cientos de voluntarios dispuestos a colaborar con la causa y vivir una experiencia única. Buscamos voluntarios para la campaña 2016. hablaremos de la importancia de la conservación de la población de tortugas marinas de Cabo Verde, de las actividades se realizan desde la ONG y de cómo participar.

Nesting In The Clouds: Evaluating And Predicting Sea Turtle Nesting Beach Parameters From Lidar Data

Humans' desire for knowledge regarding animal species and their interactions with the natural world have spurred centuries of studies. The relatively new development of remote sensing systems using satellite or aircraft-borne sensors has opened up a wide field of research, which unfortunately largely remains dependent on coarse-scale image spatial resolution, particularly for habitat modeling. For habitat-specialized species, such data may not be sufficient to successfully capture the nuances of their preferred areas. Of particular concern are those species for which topographic feature attributes are a main limiting factor for habitat use. Coarse spatial resolution data can smooth over details that may be essential for habitat characterization. Three studies focusing on sea turtle nesting beaches were completed to serve as an example of how topography can be a main deciding factor for certain species. Light Detection and Ranging (LiDAR) data were used to illustrate that fine spatial scale data can provide information not readily captured by either field work or coarser spatial scale sources. The variables extracted from the LiDAR data could successfully model nesting density for loggerhead (Caretta caretta), green (Chelonia mydas), and leatherback (Dermochelys coriacea) sea turtle species using morphological beach characteristics, highlight beach changes over time and their correlations with nesting success, and provide comparisons for nesting density models across large geographic areas. Comparisons between the LiDAR dataset and other digital elevation models (DEMs) confirmed that fine spatial scale data sources provide more similar habitat information than those with coarser spatial scales. Although these studies focused solely on sea turtles, the underlying principles are applicable for many other wildlife species whose range and behavior may be influenced by topographic features.