Post-cranial prey transport mechanisms in the black pinesnake, Pituophis melanoleucus lodingi: an x-ray videographic study

Most previous studies of snake feeding mechanisms have focused on the functional morphology of the highly specialized ophidian jaw apparatus. Although some of these studies have included observations of post-cranial movements during feeding, the functional roles of these movements have remained poorly understood. In this study, we used x-ray videography to examine post-cranial prey transport mechanisms in a colubrid snake, Pituophis melanoleucus lodingi. We found that prey transport in this species progresses through four distinct phases, three of which are characterized by either undulatory or concertina-like movements of the anterior portion of the trunk. In the first phase of transport (the oral phase), unilateral movements of the jaws are used to pull the head forward around the prey. In the second phase (the orocervical phase), unilateral jaw movements continue, but are augmented by concertina-like movements of the anterior portion of the trunk. In the third phase (the cervical phase), prey transport occurs exclusively through concertina-like movements of the neck. Finally, in the fourth phase (the thoracic phase), prey is transported to the stomach via undulatory movements of the trunk. Our observations of feeding behavior in a phylogenetically diverse sample of fourteen other snake species demonstrate that similar post-cranial transport mechanisms are used by a wide variety of alethinophidian snakes that feed on large, bulky prey.     

Transmission studies with Sarcocystis idahoensis of deer mice (Peromyscus maniculatus) and gopher snakes (Pituophis melanoleucus)

Transmission studies with Sarcocystis idahoensis of deer mice (Peromyscus maniculatus) and gopher snakes (pituophis melanoleucus) were conducted to determine host specificity of various stages of the parasite. Sporocysts were not passed by four dogs or four cats fed infected skeletal muscle from deer mice. Seven white mice (Mus musculus) and 34 white-footed mice (Peromyscus leucopus) were negative for sarcocysts and liver meronts following oral inoculation with S. idahoensis sporocysts; however, excystation of sporocysts occurred in two white-footed mice killed four hours post inoculation (PI). A gopher snake orally inoculated with sporocysts remained negative for coccidia for two months PI. Three deer mice orally inoculated and three intraperitoneally (IP) inoculated with tachyzoites from liver meronts developed sarcocysts in their skeletal muscles similar to those seen in deer mice orally inoculated with sporocysts. Liver meronts were not found. Ten deer mice orally inoculated and 10 deer mice inoculated IP with bradyzoites from S. idahoensis sarcocysts remained negative for sarcocysts and liver meronts at necropsy 17 days PI.     

Gas exchange parameters, muscle blood flow and electromechanical properties of the plantar flexors

Sixteen men were tested to determine VO2max (ml X kg-1 X min-1), anaerobic threshold VO2 (ATVO2) and oxygen kinetics (time constant, T.C.) during running on a treadmill. For measuring maximal calf blood flow (maxBF, ml X 100 ml-1 X min-1), venous occlusion plethysmography was employed immediately following a combination of arterial occlusion and toe raising exercise to exhaustion. In addition, supramaximal electrical stimulations were given to determine maximal calf twitch force (Fmax, N), maximal rate of twitch force development (dF/dt) and relaxation (R X dF/dt, N X ms-1) and electro-mechanical delay time (EMD, ms). Results demonstrated that VO2max, ATVO2 and maxBF were all inversely related to T.C. (p less than 0.05). MaxBF and ATVO2 showed the highest correlation (r = 0.89, p less than 0.01). Stepwise multiple linear regression analyses revealed that variance in VO2max (60%) and ATVO2 (84%) could be accounted for by the combined effects of the following peripheral factors: VO2max = 51,25-3.24(dF/dt) + 0.14(maxBF), and ATVO2 = 11.68 + 0.42(maxBF) - 0.2(Fmax). These findings, together with the results of cluster analysis, suggest a tight link between ATVO2 and peripheral blood flow capacity. On the other hand, a moderate correlation (r = 0.64, p less than 0.01) between VO2max and maxBF might be due in part to individual differences in oxygen extraction-utilization capacity during heavy exercise above anaerobic threshold.     

Ventilation and gas exchange in the diamondback water snake,Natrix rhombifera

Summary Simultaneous measurements of pulmonary and cutaneous oxygen and carbon dioxide exchange, pulmonary ventilation and heart rate were made on the diamondback water snake,Natrix rhombifera at 28°C using body plethysmography. Resting lung volume, maximum lung volume and tracheal volume were also measured.The following mean values were measured in undisturbed snakes breathing room air: total (pulmonary and cutaneous) O₂ uptake 46 mol · (kg min)^–1; total CO₂ output, 49 mol · (kg min)^–1; tidal volume, 12 ml (BTPS) · kg^–1; ventilatory rate, 6.9 min^–1; heart rate, 42 min^–1. From the measurements of tracheal volume, the effective (alveolar) ventilation was estimated as approximately 70% of total ventilation resulting in effective pulmonary and of 130 Torr and 20 Torr respectively. Cutaneous exchange accounted for 8.1% of the total and 12.4% of the total .Resting lung volume of anaesthetized snakes was 75 ml (BTPS) · kg^–1, maximum lung volume was 341 ml (BTPS) · kg^–1 and tracheal volume was 3.9 ml (BTPS) · kg^–1.     

The influence of gas exchange on lung gas concentrations during air breathing

A model study is made of the contribution that continuing respiratory gas exchange makes to the alveolar plateau slope for O₂ during air breathing. Calculations in the model of the O₂ concentration appearing at the mouth during expiration, are performed for single breaths of air at constant flow rates 18 litres/min and 120 litres/min. At 18 litres/min the breathing period is 5 sec, the initial lung volume is 2300 ml, and the O₂ uptake rate is 300 ml STPD/min; whereas at 120 litres/min these parameters are 4 sec, 1200 ml, and 1800 ml STPD/min respectively. In each case the initial lung O₂ tension is taken to be 98 mm Hg. It is found that at 18 litres/min, the O₂ concentration difference on the alveolar plateau over the last second of expiration is 0.4 mm Hg when gas exchange is omitted and 1.2 mm Hg when gas exchange is included in the model. At 120 litres/min, this difference is zero and 5.0 mm Hg respectively. The gas exchange component predicted from a corresponding well-mixed compartment model is the same at 18 litres/min (0.8 mm Hg) but is 6.0 mm Hg at 120 litres/min.     

Effects of curved inlet tubes on air flow and particle deposition in bifurcating lung models

In vivo bifurcating airways are complex and the airway segments leading to the bifurcations are not always straight, but curved to various degrees. How do such curved inlet tubes influence the motion as well as local deposition and hence the biological responses of inhaled particulate matter in lung airways? In this paper steady laminar dilute suspension flows of micron-particles are simulated in realistic double bifurcations with curved inlet tubes, i.e., 0 degrees < or =theta< or =90 degrees, using a commercial finite-volume code with user-enhanced programs. The resulting air-flow patterns as well as particle transport and wall depositions were analyzed for different flow inlet conditions, i.e., uniform and parabolic velocity profiles, and geometric configurations. The curved inlet segments have quite pronounced effects on air-flow, particle motion and wall deposition in the downstream bifurcating airways. In contrast to straight double bifurcations, those with bent parent tubes also exhibit irregular variations in particle deposition efficiencies as a function of Stokes number and Reynolds number. There are fewer particles deposited at mildly curved inlet segments, but the particle deposition efficiencies at the downstream sequential bifurcations vary much when compared to those with straight inlets. Under certain flow conditions in sharply curved lung airways, relatively high, localized particle depositions may take place. The findings provide necessary information for toxicologic or therapeutic impact assessments and for global lung dosimetry models of inhaled particulate matter.