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Hydrodynamic effect of a satellite transmitter on a juvenile green turtle (Chelonia mydas)

Wind tunnel tests were performed to measure the effect of a satellite transmitter on a juvenile green turtle (Chelonia mydas). A full-scale turtle model was constructed from an 11.5 kg specimen with a 48 cm carapace length, and a transmitter model was constructed from a Telonics ST-6. The turtle model was tested in a wind tunnel with and without the transmitter, which was mounted on the forward, topmost part of the carapace. Drag, lift and pitch moment were measured for several speeds and flow angles, and the data were scaled for application to the marine environment. At small flow angles representative of straight-line swimming, the transmitter increased drag by 27-30 %, reduced lift by less than 10 % and increased the pitch moment by 11-42 %. On the basis of the drag data at zero angle of attack, it is estimated that the backpack will reduce swimming speed by 11 %, assuming that the turtle produces the same thrust with the unit attached. The drag data are also used to estimate the effect of a transmitter on the swimming energetics of an adult green turtle. Design guidelines are included to minimize the adverse forces and moments caused by the transmitter.

Journal Article↗

Heart rates and diving behavior of leatherback sea turtles in the eastern pacific ocean

Heart rates and diving behavior of leatherback sea turtles (Dermochelys coriacea) were monitored at sea during the internesting interval. Instruments that recorded the electrocardiogram and the depth and duration of dives were deployed on six female leatherback turtles as they laid eggs at Playa Grande, Costa Rica. Turtles dived continually for the majority of the internesting interval and spent 57-68 % of the time at sea submerged. Mean dive depth was 19+/-1 m (mean +/- s.d.) and the mean dive duration was 7.4+/-0.6 min. Heart rate declined immediately upon submergence and continued to fall during descent. All turtles showed an increase in heart rate before surfacing. The mean heart rate during dives of 17.4+/-0.9 beats min-1 (mean +/- s.d.) was significantly lower than the mean heart rate at the surface of 24.9+/-1.3 beats min-1 (P<0.05). Instantaneous heart rates as low as 1.05 beats min-1 were recorded during a 34 min dive. The mean heart rate over the entire dive cycle (dive + succeeding surface interval; 19.4+/-1.3 beats min-1) was more similar to the heart rate during diving than to the heart rate at the surface. Although dive and surface heart rates were significantly different from each other, heart rates during diving were 70 % of heart rates at the surface, showing that leatherback turtles do not experience a dramatic bradycardia during routine diving.

Journal Article↗

Embryonic temperature influences juvenile temperature choice and growth rate in snapping turtles Chelydra serpentina.

Snapping turtles (Chelydra serpentina) demonstrate temperature-dependent sex determination (TSD): intermediate egg incubation temperatures (23-27 degreesC) produce males, while extreme temperatures produce females. Snapping turtles are also sexually dimorphic: adult males are typically larger than females. Previous researchers hypothesized that male-producing egg temperatures enhanced the growth rate of juvenile turtles, resulting in the adult dimorphism and potentially providing an adaptive benefit for TSD. In reptiles, the choice of ambient temperature can also influence growth. I measured the effect of egg incubation temperature on juvenile growth rate and water temperature choice of C. serpentina. Eggs were incubated in the laboratory at 21.5, 24.5, 27.5 or 30.5 degreesC to produce both sexes, all males, both sexes or all females, respectively. Egg temperature was linearly and negatively correlated with growth rate of both male and female juveniles. Thus, growth was enhanced, but not maximized, by male-producing egg temperatures. Egg temperature was also negatively correlated with juvenile temperature choice such that, on average, turtles from 21.5 degreesC eggs selected 28 degreesC water, while turtles from 30.5 degreesC eggs chose 24.5 degreesC water. Additionally, these temperature choices were highly repeatable, even following a 6 month hibernation period at 7 degreesC. Thus, while male egg temperatures do not directly maximize growth, multiple effects of embryonic temperature may combine to create long-lasting differences in the behavioral physiology of male and female C. serpentina. Such differences could be important to the ecology and evolution of TSD.

Journal Article↗

Properties of spinal motoneurons and interneurons in the adult turtle: provisional classification by cluster analysis.

The purpose of the present study was to compare, in motoneurons (MNs) vs. interneurons (INs), selected passive, transitional, and active (firing) properties, as recorded in slices of lumbosacral spinal cord (SC) taken from the adult turtle. The cells were provisionally classified on the basis of (1) the presence (in selected INs) or absence (MNs and other INs) of spontaneous discharge, (2) a cluster analysis of selected properties of the nonspontaneously firing cells, (3) a comparison to previous data on turtle MNs and INs, and (4) a qualitative comparison of the results with those reported for other vertebrate species (lamprey, cat). The provisional nomenclature accommodated properties appropriate for solely MNs (Main MN group) vs. nonspontaneously firing INs (Main IN-N) vs. spontaneously firing INs (IN-S) and for neurons with two degrees of intermediacy between the Main MN and the Main IN-N groups (Overlap MN, Overlap MN/IN). Morphological reconstructions of additional cells, which had been injected with biocytin during the electrophysiological tests, were shown to provide clear-cut support for the provisional classification procedure. The values for the measured parameters in the 96 tested cells covered the spectrum reported previously across adult vertebrate species and were robust in measurements made on different SC slices up to 5 days after their removal from the host animal. The interspecies comparisons permitted the predictions that (1) our Main MN and Overlap MN cells would be analogous to two MN types that innervate fast-twitch and slow-twitch skeletomotor muscle fibers, respectively, in the cat, and (2) the MNs in our Overlap MN/IN group probably innervate slow (nontwitch, tonic) muscle fibers whose presence has recently been established in the turtle hindlimb. In summary, the results bring out the utility of the SC slice preparation of the turtle for study of spinal motor mechanisms in adult tetrapod vertebrates, particularly as an adjunct to the in vivo cat, because of the ease with which robust measurements can be made of the active properties of both MNs and INs.

Action Potentials↗

Immunocytochemical localization of glutamate receptor subunits in the brain stem and cerebellum of the turtle Chrysemys picta.

The regional distribution of ionotropic (AMPA and NMDA) and metabotropic (mGluR1alpha) glutamate receptor subunits was examined in the brain stem and cerebellum of the pond turtle, Chrysemys picta, by using immunocytochemistry and light microscopy. Subunit-specific antibodies that recognize NMDAR1, GluR1, GluR4, and mGluR1alpha were used to identify immunoreactive nuclei in the brain stem and cerebellum. Considerable immunoreactivity in the turtle brain stem and cerebellum was observed with regional differences occurring primarily in the intensity of staining with the antibodies. The red nucleus, lateral reticular nucleus and cerebellum labeled intensely for NMDAR1 and moderately for GluR1. The cerebellum also labeled strongly for mGluR1alpha. All of the cranial nerve nuclei labeled intensely for NMDAR1 and to varying degrees for GluR1, GluR4, and mGluR1alpha. Counterstaining revealed the presence of neuronal somata where there were no immunoreactive neurons in individual nuclei. This finding suggests that there are subpopulations of immunoreactive neurons within a given nucleus that bear different glutamate receptor subunit compositions. The results suggest that the glutamate receptor subunit distribution in the brain stem and cerebellum of turtles is similar to that reported for rats. Additionally, there is considerable colocalization of NMDA and AMPA receptors as revealed by light microscopy. These results have implications for the organization of neural circuits that control motor behavior in turtles, and, generally, for the function of brain stem and cerebellar neural circuits in vertebrates.

Abducens Nerve↗

Scanning electron microscope studies of the papilla basilaris of some turtles and snakes.

The papillae basilares of three species of turtles and four species of snakes were studied by SEM. The papillae of turtle are relatively large among reptiles and are characterized by a long, horizontal middle section resting on wide basilar membrane. Both terminal ends of the papilla extend onto the surrounding limbus in the form of a forked or "T" -shaped end or as a curved, "hook"- like processes. Details vary with the species. In the three species of turtles studied, there were between 1,100 and 1,400 hair cells on a papilla. The tectorial membrane covering the horizontal portion of the papilla is heavy in appearance and tightly attached to the kinocilial bulbs. The terminal ends of the papilla are covered by a thin gelatinous material. In addition, mat-like tectorial network covers the supporting cells and extends from the microvilli of the supporting cells to the overlying tectorial membrane. All hair cells are unidirectionally and abneurally oriented. The supporting cell surfaces form a large part of the papilla and, thus, hair cell density is low. The papillae of the two boid snake species studied are moderately long among snakes and contain a moderate number of hair cells (574 in Epicrates and 710-780 in Constrictor). Papillar form is elongate, avoid, or canoe-shaped. The tectorial membrane may be either highly fenestrated or moderately dense and covers all but a few of the terminal hair cells. A tectorial-like mat covers all but a few of the terminal hair cells. Most hair cells are unidirectionally and abneurally oriented. A few terminal cells in boids may show reverse orientation. Hair cell density is similar to that of turtles.

Animals↗

Growth of the turtle Chrysemys scripta under constant controlled laboratory conditions.

The purpose of this study was to determine 1) growth of the turtle shell and change in weight under constant controlled laboratory conditions and 2) whether under these constant conditions there were seasonal changes. Fifty unfed refrigerated eight-week-old hatchling turtles Chrysemys scripta were received in October and maintained in aquaria with 16 hours of artificial light and eight hours of darkness, at 24-27 degrees C and a humidity of 30% and fed twice weekly. Gross linear measurements of the width and length of the plastron and carapace, and total body weights, were taken at eight weeks and thereafter at about six-week intervals. During the two-year period the mean increase of the plastron length was from 30.79 +/- 0.19 mm to 68.32 +/- 1.58 mm, plastron width from 24.23+/- 0.20 mm to 50.43 +/- 1.03 mm; carapace length from 32.47 +/- 0.24 mm to 75.21 +/- 1.82 mm, carapace width from 31.81 +/- 0.28 mm to 67.12 +/- 1.29 mm, and body weight from 6.94 +/- 0.15 gm to 80.63 +/- 5.02 gm. Calculated daily percent changes revealed that strongly correlated with its value at 786 days of age. No seasonal differences in growth were noted between the summer and winter periods when turtles would enter winter dormancy in certain natural environments. Environmental factors are reflected in the growth of the turtle.

Animals↗

Cutaneous dermatomes for initiation of three forms of the scratch reflex in the spinal turtle.

The turtle spinal cord produces three forms of the hindlimb scratch reflex. Each scratch form is initiated in response to gentle mechanical stimulation of a distinct set of sites in the periphery, termed the receptive field for that scratch form. The turtle spinal cord consists of 8 cervical segments (C1-C8), 10 dorsal segments (D1-D10), 2 sacral segments (S1, S2), and about 16 caudal segments (Ca1-Ca16). First, we recorded cutaneous afferents in peripheral nerves to reveal the tactile dermatomes of segments D3-D8. These segments innervate regions of the body between the forelimb and hindlimb, directly lateral to their spinal cord segments. Adjacent segments innervate adjacent and partially overlapping regions of the periphery. Second, we used successive spinal cord transections combined with either a) behavioral analysis in turtles with limb movements or b) electroneurographic recordings in immobilized turtles, and mapped the zone of remaining sensibility after each transection to measure the borders of dermatomes D2-Ca2. This technique revealed that adjacent dermatomes are innervated by non-adjacent spinal segments in regions near the hip. Segments D8 and Ca1 innervate adjacent and partially overlapping regions ventral to the hip. There is a similar discontinuity in the innervation of the shell and skin dorsal to the hip. These discontinuities correlate with the innervation of the hindlimb skin by segments D8-Ca1. The rostral scratch receptive field is innervated by sensory afferents entering spinal segments D3-D6; the pocket scratch receptive field is innervated by D6-D8; the caudal scratch receptive field is innervated by S2, Ca1, and more caudal segments. The rostral-pocket transition zone is innervated mainly by one segment, D6; the ventral part of the caudal-pocket transition zone is innervated by two non-adjacent segments, D8 and Ca1. Thus the motor pattern blends elicited by stimulation of sites within the rostral-pocket transition zone must be produced in response to a very different distribution of sensory inputs than the blends elicited by stimulation of sites within the caudal-pocket transition zone.

Action Potentials↗

Neuroanatomical distribution and binding properties of saxitoxin sites in the rat and turtle CNS.

Since saxitoxin (STX) binds to voltage-sensitive sodium channels and blocks their function, it has been widely used in the study of these channels. There is, however, limited information on STX binding properties and the neuroanatomical distribution of the Na+ channel as a function of brain region in the rat and in lower vertebrates such as the turtle. In the present study, we used a broad range of 3H-STX concentration (up to 64 nM) to examine saturation profiles and density distribution in both adult rat and turtle brains. We found that (1) STX sites do not vary greatly in affinity (most Kds = 2 to 5 nM) in various regions of the adult rat brain; (2) STX binding distribution was very heterogeneous in the rat with much higher density in the cortex, hippocampus, amygdala, and cerebellum than in the brainstem and spinal cord; (3) STX sites are mostly localized in layers made mostly of neurons with low density in white matter; and (4) turtle brain STX sites had similar binding properties, but its brain had much fewer STX sites than the rat, especially in the cerebellum and rostral areas such as the cortex. We conclude that (a) adult brain sodium channels have similar STX binding affinity in spite of the existence of multiple sodium channel subtypes; (b) the brainstem is very different from rostral brain areas in channel density; and (c) the turtle brain has a much lower sodium channel density than the rat brain.

Animals↗

Anatomical organization of the limb premotor network in the turtle (Chrysemys picta) revealed by in vitro transport of biocytin and neurobiotin.

The in vitro turtle brainstem-cerebellum preparation has been a valuable tool in the study of central motor programs. In the present study, we investigate the anatomical organization of the turtle rubrocerebellar limb premotor network and its sensory connections in vitro by combining the rapid anterograde and retrograde transport of neurobiotin and biocytin with the extended viability of the isolated turtle brainstem-cerebellum. These compounds retrogradely labeled soma, dendrites, and axons, and orthogradely labeled axons and, to a lesser extent, terminals. The chelonian red nucleus receives a dense input from the contralateral lateral cerebellar nucleus and projects heavily to the contralateral spinal cord. Rubral axons sparsely innervate the lateral cerebellar nucleus and project heavily to the lateral reticular nucleus. Lateral reticular axons heavily innervate the lateral cerebellar nucleus before terminating in the pars lateralis of the cerebellar cortex as mossy fibers. These prominent, recurrent loops among the lateral cerebellar nucleus, red nucleus, and lateral reticular nucleus constitute the turtle rubrocerebellar limb premotor network. Sensory inputs to the red nucleus originate in the contralateral dorsal column nuclei, the principal trigeminal nucleus, and the spinothalamic system. These sites project bilaterally to the lateral reticular nucleus. The lateral cerebellar nucleus receives a contralateral input from the dorsal column nuclei. The red nucleus projects sparsely to the dorsal column nuclei. The red nucleus also receives an ipsilateral descending projection from the suprapeduncular nucleus, located in the diencephalon, and an ascending input from the rostral rhombencephalic reticular formation. An ipsilateral descending pathway originating in the red nucleus is likely to be the rubro-olivary tract.

Animals↗

Expression of SR-BI (Scavenger Receptor Class B Type I) in turtle (Chrysemys picta) tissues and other nonmammalian vertebrates.

In this study, the tissue distribution of the expression of an HDL-receptor (SR-BI; Scavenger Receptor Class B Type I) was investigated in the turtle using an antiserum to murine SR-BI. Several turtle tissues including liver, heart, small intestine, kidney, oviduct, ovary, and testis were shown to express an 82 kDa membrane protein. In addition, SR-BI expression in livers of other nonmammalian species such as the chicken, frog, goldfish, shark, and skate is also reported. Ovarian SR-BI expression varies seasonally in the turtle as do plasma levels of apoA-I and cholesterol ester. It is possible that changing levels of SR-BI, the receptor for apoA-I, is physiologically relevant to the demands of the turtle ovarian cycle and cholesterol distribution.

Adaptation, Physiological↗

Nitrogen metabolism and excretion in the aquatic chinese soft-shelled turtle, Pelodiscus sinensis, exposed to a progressive increase in ambient salinity.

This study aimed to determine effects of 6-day progressive increase in salinity from 1 per thousand to 15 per thousand on nitrogen metabolism and excretion in the soft-shelled turtle, Pelodiscus sinensis. For turtles exposed to 15 per thousand water on day 6, the plasma osmolality and concentrations of Na+, Cl- and urea increased significantly, which presumably decreased the osmotic loss of water. Simultaneously, there were significant increases in contents of urea, certain free amino acids (FAAs) and water-soluble proteins that were involved in cell volume regulation in various tissues. There was an apparent increase in proteolysis, releasing FAAs as osmolytes. In addition, there might be an increase in catabolism of certain amino acids, producing more ammonia. The excess ammonia was retained as indicated by a significant decrease in the rate of ammonia excretion on day 4 in 15 per thousand water, and a major portion of it was converted to urea. The rate of urea synthesis increased 1.4-fold during the 6-day period, although the capacity of the hepatic ornithine urea cycle remained unchanged. Urea was retained for osmoregulation because there was a significant decrease in urea excretion on day 4. Increased protein degradation and urea synthesis implies greater metabolic demands, and indeed turtles exposed to 15 per thousand water had significantly higher O2 consumption rate than the freshwater (FW) control. When turtles were returned from 15 per thousand water to FW on day 7, there were significant increases in ammonia (probably released through increased amino acid catabolism) and urea excretion, confirming that FAAs and urea were retained for osmoregulatory purposes in brackish water.

Amino Acids↗

Cytological evaluation of spermatogenesis and organization of the germinal epithelium in the male slider turtle, Trachemys scripta.

The germ cell development in the slider turtle (Trachemys scripta) testis was investigated by viewing the histology of the seminiferous epithelium in plastic sections with a light microscope. Germ cell morphologies in the slider turtle testis were similar to the morphologies of other vertebrate germ cell types. However, the slider turtle seminiferous epithelium contained germ cells that progress through spermatogenesis in a temporal rather than a spatial pattern, resulting in a single spermatogenic event that climaxed with one massive sperm release in November. Mature sperm then are stored within the epididymis until breeding commences in the following spring. The germ cell development strategy in the slider turtle is different from that of other amniotes and is more reminiscent of the developmental strategy found in the anamniotic testis. This temporal progression of germ cells through spermatogenesis within a tubular testis represents a transitional model that may be evolutionarily significant.

Animals↗

The buccopharyngeal mucosa of the turtles (testudines).

Gross and histological examination of all extant families of turtles revealed that the buccopharyngeal mucosa is morphologically highly varied. The tongues of aquatic species have small lingual papillae or lack them entirely, while terrestrial species have tongues with numerous glandular papillae. The pharynx and the esophagus also have papillae in some species. These either facilitate swallowing in which case they are long, pointed, keratinized, and occur commonly in marine turtles, or they are vascular and nonkeratinized, facilitate respiratory gas exchange and are found in the Trionychidae, Dermatemyidae, and Carettochelyidae. The morphology of the buccopharyngeal mucosa of turtles reflects their diet, feeding behavior, habitat, and relationships. Convergence in the morphology of the buccopharyngeal mucosa occurs among families, especially among the Emydidae and other familes of turtles. Intergeneric parallelism is also seen within the Emydidae.

Animals↗

Evidence for GABAergic interneurons in the red nucleus of the painted turtle.

Immunocytochemical and electrophysiological evidence supporting the presence of GABAergic interneurons in the turtle red nucleus is presented. Injections of HRP into the spinal cord produced labeling of large neurons in the contralateral red nucleus. The peroxidase-antiperoxidase (PAP) method revealed smaller cells immunoreactive to an antibody against glutamate decarboxylase (GAD), the synthetic enzyme for the inhibitory neurotransmitter GABA, that were interspersed among larger immunonegative neurons. Similar small neurons were densely immunostained by antibodies to GABA-glutaraldehyde conjugates obtained from different sources and applied according to pre-embedding and postembedding protocols. Rubrospinal neurons retrogradely labeled with HRP measured 16 and 27 microns in mean minor and major cell body diameters, while GABA-like immunopositive neurons situated within the red nucleus measured 7 and 13 microns. There was very little overlap in soma size between the two cell populations. Therefore, we suggest that the GAD- and GABA-positive neurons may be local inhibitory interneurons. This notion is further supported by observations of pre-embedding immunostaining for GAD and postembedding immunostaining for GABA showing that the turtle red nucleus is amply innervated by immunoreactive axon terminals. These puncta are closely apposed to cell bodies and dendrites of both immunonegative large neurons and immunopositive small neurons. Moreover, immunogold staining at the electron microscopic level demonstrated that GABA-like immunoreactive axon terminals with pleomorphic synaptic vesicles formed symmetric synapses with cell bodies and dendrites of the two types of red nucleus cells. These ultrastructural features are commonly assumed to indicate inhibitory synapses. A moderately labeled bouton with round vesicles and asymmetric synapses was also observed. In addition, the two types of red nucleus neurons received asymmetric axosomatic and axodendritic synapses with GABA-negative boutons provided with round vesicles, features usually associated with excitatory functions. To obtain electrophysiological evidence for inhibition, intracellular recordings from red nucleus neurons were conducted using an in vitro brainstem-cerebellum preparation from the turtle. Small, spontaneous IPSPs were recorded from 7 out of 14 red nucleus cells studied. These morphological and physiological results provide strong support for concluding that the turtle red nucleus, like its mammalian counterpart, contains GABAergic inhibitory interneurons. While we have not identified the main source of input to these interneurons, in view of the scarce development of the reptilian cerebral cortex, this input is unlikely to come from the motor cortex as it does in mammals.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗

Identification of sex in hatchling loggerhead turtles (Caretta caretta) by analysis of steroid concentrations in chorioallantoic/amniotic fluid.

A major difficulty in sea turtle conservation is the inability to nonlethally and noninvasively identify the sex of hatching sea turtles. Traditional sexing techniques such as plasma sex steroid quantification cannot be applied to hatchlings without sacrificing the hatchlings or utilizing invasive procedure. This paper presents a technique for sexing hatchling sea turtles by analysis of sex steroid concentrations in egg chorioallantoic/amniotic fluid (CAF). Metabolites of estradiol-17 beta (E) and testosterone (T) in CAF are best expressed as an index or E:T ratio. Chorioallantoic/amniotic fluid E:T ratios for males (0.5 +/- 0.1) were significantly lower than those for females (2.2 +/- 0.3). When separated by utilizing an E:T ratio of 1.25 as the determinant index value, 27 of 28 hatchlings were designated correctly as males (E:T < 1.25) or females (E:T > or = 1.25). Sex was verified for all hatchlings by gonadal histology. This study shows significant concentrations of T and E metabolites in CAF and plasma of hatchling loggerhead turtles and illustrates the use of a nonlethal, noninvasive method for determining sex, which could be potentially utilized for other endangered reptile and avian species.

Amniotic Fluid↗

Adrenomedullary hormonal and glycemic responses to high ambient temperature in the soft-shelled turtle, Lissemys punctata punctata.

The aim of the investigation was to study the influence of high ambient temperature on adrenomedullary activity and blood glucose levels in adult female soft-shelled turtles (Lissemys punctata punctata). Experiments were carried out at 25 degrees, 35 degrees, and 38 degrees, and one group was exposed to 38 degrees for 15 days and then maintained at 25 degrees for another 15 days. Exposure to a low ambient temperature of 25 degrees had no clear effect on adrenomedullary function with respect to histology (nuclear diameter), epinephrine and norepinephrine concentrations, and blood glucose level of turtles, but higher temperatures of 35 degrees and 38 degrees stimulated adrenomedullary activity as well as blood glucose level in turtles compared with controls (30 degrees ). The extent of these changes was greater at 38 degrees than that at 35 degrees, and withdrawal from high ambient temperature reversed the effect in turtles.

Adrenal Medulla↗

The implications of variable remigration intervals for the assessment of population size in marine turtles.

Sea turtles nest on sandy beaches and tend to show high fidelity to specific nesting areas, but, despite this fidelity, the inter-annual variation in nesting numbers may be large. This variation may reflect the fact that turtles do not usually nest in consecutive years. Here, theoretical models are developed in which the interval between successive nesting years (the remigration interval) reflects conditions encountered on the feeding grounds, with good feeding years leading to a reduction in the remigration interval and vice versa. These simple models produce high levels of inter-annual variation in nesting numbers with, on occasion, almost no turtles nesting in some years even when the population is large and stable. The implications for assessing the size of sea turtle populations are considered.

Animals↗