Seasonal changes in blood oxygen transport and acid-base status in the tegu lizard, Tupinambis merianae

Oxygen-binding properties, blood gases, and acid-base parameters were studied in tegu lizards, Tupinambis merianae, at different seasons and temperatures. Independent of temperature and pH, blood oxygen affinity was higher in dormant lizards than in those active during the summer. Haematocrit (Hct) and hemoglobin content ([Hb]) were greater in active lizards resulting in a higher oxygen-carrying capacity. Nucleoside triphosphate content ([NTP]) was reduced during dormancy, but the ratio between [NTP] and [Hb] remained unchanged. Dormancy was accompanied by an increase in plasma bicarbonate ([HCO(3)(-)]PI) and an elevation of arterial CO(2) partial pressure (P(aCO2)) and CO(2) content in the plasma (C(PlCO2)). These changes in acid-base parameters persist over a broad range of body temperatures. In vivo, arterial O(2) partial pressure (Pa(O2)) and O(2) content (Ca(O2)) were not affected by season and tended to increase with temperature. Arterial pH (pH(a)) of dormant animals is reduced compared to active lizards at body temperatures below 15 degreesC, while no significant difference was noticed at higher temperatures. (C) 2003 Elsevier B.V. All rights reserved.

Frugivoria e dispersão de sementes pelo lagarto teiú Tupinambis merianae (Reptilia: Teiidae)

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Structure of the posthepatic septum and its influence on visceral topology in the tegu lizard, Tupinambis merianae (Teiidae : Reptilia)

The posthepatic septum (PHS) divides the body cavity of Tupinambis merianae into two parts: the cranial one containing the lungs and liver and the caudal one containing the remaining viscera. The PHS is composed of layers of collagenous fibers and bundles of smooth muscle, neither of which show systematic orientation, as well as isolated blood vessels, lymphatic vessels, and nerves. Striated muscle of the abdominal wall does not invade the PHS. The contractions of the smooth muscles may stabilize the pleurohepatic cavity under conditions of elevated aerobic needs rather than supporting breathing on a breath-by-breath basis. Surgical removal of the PHS changes the anatomical arrangement of the viscera significantly, with stomach and intestine invading the former pleurohepatic cavity and reducing the space for the lungs, Thus, the PHS is essential to maintain the visceral topography in Tupitionibis. J. Morphol. 258:151-157, 2003. (C) 2003 Wiley-Liss. Inc.

Role of the post-hepatic septum on breathing during locomotion in Tupinambis merianae (Reptilia : Teiidae)

Tupinambis merianae increased minute ventilation by increasing both tidal volume and breathing frequency during sustained locomotion at 0.17 m s(-1). Animals in which the post-hepatic septum (PHS) had been surgically removed were not able to increase tidal volume during locomotion. Tegus without PHS compensated, in part, by increasing breathing frequency above the levels observed for tegus with intact PHS, but minute ventilation remained less than in the control animals. The rate of oxygen consumption and the air convection requirement, however, were not significantly different between animals with and without PHS, nor at the tested speeds was endurance affected by the removal of the PHS. These data suggest that the PHS facilitates ventilation by acting as a mechanical barrier, preventing the viscera from moving cranially during physical exertion.

Allometry and morphological integration in the skull of Tupinambis merianae (Lacertilia: Teiidae)

The morphogenetic processes acting in the skull of the lizard Tupinambis merianae were investigated by geometric morphometric techniques. The observed ontogenetic shape change involved a widening of the anterior extremity, stretching and narrowing of the midface, narrowing of the braincase, orbital reduction and elongation of the temporal region (origin of jaw adductor muscles). This change occurred mostly in a localized way in certain cranial regions. The major components identified were: rostrum, midface, dermal elements of braincase (functionally influenced) and endochondral elements of braincase (embryologically influenced). The growth patterns lead to an increased robustness of the skull (particularly the anterior extremity) and a reduction of cranial kinesis. These changes, together with the ontogenetic variation in dentition aid in the ontogenetic variation observed in the diet of these animals, which shift from carnivory to omnivory.

Estudo da helmintofauna do lagarto Tupinambis merianae Dumeril e Bibron, 1839 (Reptilia: Squamata, Teiidae) procedentes do arquipélago de Fernando de Noronha, Pernambuco, Brasil e relação com a fauna endêmica de lagartos do arquipélago

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Variação sazonal da temperatura corpórea no lagarto Teiú, Tupinambis merianae (Squamata, Lacertilia, Teiidae)

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Caracterização histomorfométrica do intestino delgado do lagarto Teiú, Tupinambis merianae, em resposta à dormência sazonal e alimentação

O teiú, Tupinambis merianae, é um lagarto Teiidae comum na América do Sul, e conhecido por apresentar um ciclo anual de atividade bastante marcante. Reprodução e forrageio ocorrem nos meses quentes do ano e, com o inicio dos meses mais frios, os animais param de se alimentar, escondem-se em tocas escavadas no solo e hibernam de 4-5 meses consecutivos, em temperaturas médias por volta de 17°C. Considerando que durante a dormência sazonal o teiú permanece por um longo período sem se alimentar e que o epitélio do intestino pode responder à ausência/presença de nutrientes luminais através de ajustes morfológicos e funcionais importantes, no presente trabalho nós analisamos as alterações histomorfológicas do intestino delgado do lagarto teiú, T. merianae, em função do jejum sazonal e não sazonal, bem como em resposta à ingestão do alimento. Para tanto, acompanhamos as alterações dos parâmetros estudados em três grupos experimentais: G1, animais amostrados logo após a saída da dormência e antes (i.e., após o jejum sazonal) e após a primeira alimentação pós-dormência; G2, antes e após a segunda alimentação pósdormência; e G3, grupo submetido a um jejum extra de 60 dias após o despertar da dormência. Foram analisados cortes de cada amostra de tecido, sendo que em cada corte foram realizadas as seguintes medidas morfométricas: altura de vilosidades, espessura da camada muscular, perímetro do intestino e contagem de células caliciformes por vilosidade. Nossos resultados indicam a ocorrência de uma atrofia da mucosa intestinal em resposta ao jejum suplementar (60 dias) e um aumento desta em resposta a alimentação (para todos os grupos). Houve também uma diminuição do perímetro intestinal com o jejum suplementar (60 dias) e uma diminuição do número de células caliciformes em animais em jejum. Também durante o jejum, o epitélio intestinal... (Resumo completo, clicar acesso eletrônico abaixo)

Efeitos da dieta e ontogenia no crescimento e fisiologia digestiva do lagarto Teiu, Tupinambis Merianae

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Efeitos da dieta e ontogenia no crescimento e fisiologia digestiva do lagarto Teiu, Tupinambis Merianae

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Helminths From an Introduced Species (Tupinambis merianae), and Two Endemic Species (Trachylepis atlantica and Amphisbaena ridleyi) From Fernando de Noronha Archipelago, Brazil

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Density of the tegu lizard (Tupinambis merianae) and its role as nest predator at Anchieta Island, Brazil

Mammals has been pointed out to be the main nest predators in islands, but recent studies has shown that tree snakes are also important nest predator in tropical forests. Here we present information on the density tegu lizards Tupinambis merianae and its role as nest predator at Anchieta Island, Ubatuba, in southeastern Brazil. The mean density of tegu lizards wets estimated to be 83 individuals/km2, which is 1.83 times lower than other well-known population (Fernando de Noronha Archipelago). In the dense rainforest, the density was estimated in 20 individuas/ km2, and in the open rainforest, 109 ind/km2. The high density of this lizard may have serious implications for nest predation. We found that 36% of artificial plasticine eggs were "preyed upon" by tegu lizards. Therefore, it is paramount to manage the tegu population on Anchieta Island to assure the survival of ground nesting birds in islands and possibly in forest fragments.

Seasonal metabolic depression, substrate utilisation and changes in scaling patterns during the first year cycle of tegu lizards (Tupinambis merianae)

The tegus increase in body mass after hatching until early autumn, when the energy intake becomes gradually reduced. Resting rates of oxygen consumption in winter drop to 20% of the values in the active season (Vo(2)=0.0636 ml g(-1) h(-1)) and are nearly temperature insensitive over the range of 17-25degreesC (Q(10)=1.55). During dormancy, plasma glucose levels are 60% lower than those in active animals, while total protein, total lipids and beta-hydroxybutyrate are elevated by 24%, 43% and 113%, respectively. In addition, a significant depletion of liver carbohydrate (50%) and of fat deposited in the visceral fat bodies (24%) and in the tail (25%) and a slight loss of skeletal muscle protein (14%) were measured halfway through the inactive period. Otherwise, glycogen content is increased 4-fold in the brain and 2.3-fold in the heart of dormant lizards, declining by the onset of arousal. During early arousal, the young tegus are still anorexic, although Vo(2) is significantly greater than winter rates. The fat deposits analysed are further reduced (62% and 45%, respectively) and there is a large decrease in tail muscle protein (50%) together with a significant increase in glycogen (2-3-fold) and an increase in plasma glucose (40%), which suggests a role for gluconeogenesis as a supplementary energy source in arousing animals. No change is detectable in citrate synthase activity, but beta-hydroxyacyl CoA dehydrogenase activities are strongly affected by season, reaching a Mold and 5-fold increase in the liver tissue of winter and arousing animals, respectively, and becoming reduced by half in skeletal muscle and heart of winter animals compared with late fall or spring active individuals. From hatching to late autumn, the increase of the fat body mass relatively to body mass is disproportionate (b=1.44), and the mass exponent changes significantly to close to 1.0 during the fasting period. The concomitant shift in the Vo(2) mass exponent in early autumn (b=0.75) to values significantly greater than 1.0 in late autumn and during winter dormancy indicates an allometric effect on the degree of metabolic depression related to the size of the fat stores and suggests greater energy conservation in the smaller young.

Metabolic response to feeding in Tupinambis merianae: Circadian rhythm and a possible respiratory constraint

The diurnal tegu lizard Tupinambis merianae exhibits a marked circadian variation in metabolism that is characterized by the significant increase in metabolism during part of the day. These increases in metabolic rate, found in the fasting animal, are absent during the first 2 d after meal ingestion but reappear subsequently, and the daily increase in metabolic rate is added to the increase in metabolic rate caused by digestion. During the first 2 d after feeding, priority is given to digestion, while on the third and following days, the metabolic demands are clearly added to each other. This response seems to be a regulated response of the animal, which becomes less active after food ingestion, rather than an inability of the respiratory system to support simultaneous demands at the beginning of digestion. The body cavity of Tupinambis is divided into two compartments by a posthepatic septum (PHS). Animals that had their PHS surgically removed showed no significant alteration in the postprandial metabolic response compared to tegus with intact PHS. The maximal metabolic increment during digestion, the relative cost of meal digestion, and the duration of the process were virtually unaffected by the removal of the PHS.

Gas exchange and ventilation during dormancy in the tegu lizard Tupinambis merianae

The tegu lizard Tupinambis merianae exhibits an episodic ventilatory pattern when dormant at 17 degrees C but a uniform ventilatory pattern when dormant at 25 degrees C. At 17 degrees C, ventilatory episodes were composed of 1-22 breaths interspaced by non-ventilatory periods lasting 1.8-26min, Dormancy at the higher body temperature was accompanied by higher rates of O-2 consumption and ventilation. The increase in ventilation was due only to increases in breathing frequency with no change observed in tidal volume. The air convection requirement for O-2 did not differ at the two body temperatures. The respiratory quotient was 0.8 at 17 degrees C and 1.0 at 25 degrees C. We found no consistent relationship between expired gas composition and the start/end of the ventilatory period during episodic breathing at 17 degrees C. However, following non-ventilatory periods of increasing duration, there was an increase in the pulmonary O-2 extraction that was not coupled to an equivalent increase in elimination of CO2 from the lungs. None of the changes in the variables studied could alone explain the initiation/termination of episodic ventilation in the tegus, suggesting that breathing episodes are shaped by a complex interaction between many variables. The estimated oxidative cost of breathing in dormant tegus at 17 degrees C was equivalent to 52.3% of the total metabolic rate, indicating that breathing is the most costly activity during dormancy.