Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “Turtles”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 775 records · Page 43Linked to original sources

Cope's rule in cryptodiran turtles: do the body sizes of extant species reflect a trend of phyletic size increase?

Cope's rule of phyletic size increase is questioned as a general pattern of body size evolution. Most studies of Cope's rule have examined trends in the paleontological record. However, neontological approaches are now possible due to the development of model-based comparative methods, as well as the availability of an abundance of phylogenetic data. I examined whether the phylogenetic distribution of body sizes in extant cryptodiran turtles is consistent with Cope's rule. To do this, I examined body size evolution in each of six major clades of cryptodiran turtles and also across the whole tree of cryptodirans (n = 201 taxa). Extant cryptodiran turtles do not appear to follow Cope's rule, as no clade showed a significant phyletic body size trend. Previous analyses in other extant vertebrates have also found no evidence for phyletic size increase, which is in contrast to the paleontological data that support the rule in a number of extinct vertebrate taxa.

Animals↗

Observations on Haemogregarina balli sp. n. from the common snapping turtle, Chelydra serpentina.

Haemogregarina balli sp. n. is described from the blood and organs of the common snapping turtle Chelydra serpentina serpentina and from the gastric and intestinal ceca of the presumed invertebrate hosts, the leeches Placobdella parasitica and Placobdella ornata. In the peripheral blood of the turtle, male and female gametocytes and immature erythrocytic schizonts are found within erythrocytes. The maturation of erythrocytic schizonts containing 6-8 merozoites is recorded from liver imprints. Schizonts with 13-25 merozoites are found in various cells of the liver, lung and spleen. In the gastric ceca of the leeches the host erythrocytes are digested, releasing the gametocytes and immature erythrocytic schizonts. Immature erythrocytic schizonts degenerate. Association of the gametocytes occurs in the intestinal ceca. The microgametocyte apparently gives rise to 4 nonmotile microgametes, one of which fertilizes the macrogamete while the other remain as condensed' residual nuclei on the periphery of the developing oocyst. The oocyst increases in size with maturity. A mature oocyst produces 8 sporozoites from a single germinal center. Sporozoites liberated from the oocyst are found in the tissues of the leech. Transovarial transmission of the parasite does not occur in the turtle. Attempts at experimental transmission failed. Previously unfed (control) leeches were negative for the parasite. Haemogregarina balli is compared with other haemogregarines described from C. serpentina. Features of species of Haemogregarina and Hepatozoon as well as the taxonomy of these genera are discussed.

Animals↗

Contrast radiography of the gastrointestinal tract in sea turtles.

Intestinal obstruction by radiolucent foreign bodies is common in sea turtles. The absence of clinical signs and the extended fasting periods in these animals means that intestinal obstructions may not be diagnosed early. Digestive tract radiographic contrast procedures were performed to evaluate the gastrointestinal transit time and intestinal obstructions in loggerhead sea turtles. Barium sulfate and nonionic iodinate contrast medium were used for radiographic contrast procedures. Contrast medium was administered via a gastric tube or into the colon. These procedures are often necessary and are useful to document intestinal obstruction and foreign objects. The diagnostic procedures were not easily performed in some turtles, but often they were adequate for the diagnosis.

Animals↗

Spinal motor patterns in the turtle.

Rhythmic alternation between ipsilateral hip flexors and extensors occurs during the normal pattern of fictive rostral scratching in response to unilateral midbody stimulation in D3-end turtles (complete spinal transection posterior to the forelimb enlargement). Unilateral midbody stimulation evokes rhythmic bursts of ipsilateral hip flexor activity with no hip extensor activity in D3-end turtles with D6-D7 contralateral hemisection (transverse hemisection anterior to the hindlimb enlargement). Bilateral midbody stimulation in these turtles evokes reconstruction of rhythmic alternation between intact side hip flexors and extensors. These normal motor patterns in response to two-site stimulation are reconstructed because one-site stimulation in this preparation activates only hip flexor rhythms (J. Neurosci. 18: 467). Hip flexor rhythms can therefore occur without hip extensor activation. This supports the concept that reciprocal inhibition between flexor and extensor interneurons is not required for flexor motor rhythm generation. Reciprocal inhibition, when present, also contributes to rhythmicity (J. Neurophysiol. 78: 3479; see also Currie and Gonsalves, this volume). Both mechanisms for rhythmicity are included in the Grillner unit burst generator model: hip flexor unit burst generators may be rhythmogenic in the absence of hip extensor activity and reciprocal inhibition contributes to rhythmogenesis. Contralateral midbody stimulation assisted in the activation of ipsilateral hip extensor rhythmicity during reconstructed rostral scratching. This result provides additional support for the hypothesis that a bilateral shared core of hip interneuronal circuitry plays a critical role in the generation of the normal pattern of fictive rostral scratching (J. Neurosci. 15: 4343).

Animals↗

Surgical removal of a fish hook from the oesophagus of a turtle.

An adult male Macquarie turtle was presented for examination after swallowing a fish hook. Radiographs taken to determine the position of this foreign body within the gastrointestinal tract revealed the fish hook lodged in the turtle's oesophagus. Surgical removal of the fish hook involved an approach through the soft tissues of the lateral neck. The turtle recovered well and was returned to the wild.

Animals↗

Functional characteristics of slowly adapting pulmonary stretch receptors in the turtle (Chrysemys picta).

1. Single nerve fibre discharge has been recorded from slowly adapting pulmonary stretch receptors in single-pithed turtles on artificial ventilation. 2. Receptor discharge during static and dynamic lung inflations showed that lung volume was the major stimulus of these receptors. The rate and degree of change in transpulmonary pressure were without direct effect. 3. The response of these receptors to static and dynamic lung inflation differed only quantitatively from those of bronchopulmonary stretch receptors in mammals. The lower discharge frequencies and sensitivities of the turtle receptors may arise from the low body temperature of these animals. 4. The sensitivity of turtle pulmonary receptors to CO2 was greater than that recorded for bronchopulmonary receptors of mammals although the effects of CO2 on receptor discharge were qualitatively similar. In several instances, receptor discharge was totally inhibited throughout the ventilatory cycle by inflation with 5--10% CO2 in air.

Action Potentials↗

Response properties of motoneurones in a slice preparation of the turtle spinal cord.

1. Motoneurones in transverse sections of the turtle spinal cord were investigated in vitro with intracellular recording techniques. 2. Turtle motoneurones had a resting membrane potential of -60 to -80 mV, spike height of 90-110 mV and were able to maintain rhythmic firing during depolarization. In agreement with the size variation of the cells the input resistance and time constant ranged from 18 M omega and 12 ms to 55 M omega and 61 ms. 3. The active response properties of motoneurones included time-dependent inward rectification in response to hyperpolarizing current pulses. The action potential had an initial segment (IS) and a soma-dendritic (SD) component and was followed by a fast and a slow after-hyperpolarization (AHP) with different sensitivity to membrane potential. 4. The relation between firing rate and injected current was sigmoid when determined for the first few interspike intervals during depolarizing current pulses. Adaptation was biphasic with an early phase lasting 0.5-1 s and a late phase lasting 10-20 s. 5. The ionic conductances responsible for the active membrane properties included a tetrodotoxin (TTX)-sensitive Na+ conductance generating the action potential and a Ca2+ conductance transiently activated during the action potential. A tetraethylamonium (TEA)-sensitive K+ conductance was responsible for spike repolarization and the fast AHP. A Ca2+-dependent K+ conductance, blocked by Mn2+ and apamin, accounted for only part of the slow AHP. The time-dependent inward rectification was selectively blocked by extracellular Cs+ at concentrations below 1 mM. 6. The results show that the response properties of spinal motoneurones of the turtle are closely similar to those known from mammals in vivo. The experiments confirm and extend the identification of the ionic conductances underlying the active response properties of spinal motoneurones.

Action Potentials↗

Intrinsic determinants of firing pattern in Purkinje cells of the turtle cerebellum in vitro.

1. The intrinsic response properties of turtle Purkinje cells and the underlying conductances have been investigated with intradendritic and intrasomatic recordings in a slice preparation. 2. The active generation site for fast Na+ spikes was confined to the soma and for slow Ca2+ spikes to the dendrites. The configuration and generation of Ca2+ spikes was more affected by the level of extracellular K+ than were Na+ spikes. 3. Sodium spikes had a lower threshold than Ca2+ spikes at all recording sites. Sodium spike firing was abruptly initiated during depolarizing current pulses and the spike frequency increased from an early minimum to a higher steady-state level over a period of seconds or until the occurrence of Ca2+ spikes. Calcium spikes were always delayed by at least 100 ms from the onset of a depolarizing current pulse from rest. 4. The abrupt onset of Na+ spike firing was due to a tetrodotoxin-sensitive plateau potential. The phase of accelerating firing frequency and the delayed occurrence of Ca2+ spikes was due to a transient hyperpolarization activated by depolarization from rest or from more negative membrane potentials. The transient hyperpolarization was inactivated by depolarized holding potentials and was most probably generate by a rapidly inactivating K+ channel. 5. It is concluded that turtle Purkinje cells display the basic firing properties and underlying conductances known from Purkinje cells of other vertebrates. In turtle Purkinje cells Ca2+ spikes are actively generated in spiny dendrites and it is suggested that spiny dendrites rather than branch points are 'hot spots'. 6. The transient hyperpolarization, not previously described in Purkinje cells, seems particularly important for regulating Ca2+-dependent excitability.

Action Potentials↗

Decoupling of horizontal cells in carp and turtle retinae by intracellular injection of cyclic AMP.

1. Horizontal cells are electrically coupled through gap junctions. This is a disadvantage in elucidating the membrane properties of the cells. In order to block gap junctions, adenosine 3',5'-cyclic monophosphate (cyclic AMP) or its analogues, dibutyryl cyclic AMP and 8-bromo cyclic AMP, were ionophoretically injected into horizontal cells of the carp or turtle retina. 2. Before injection of the chemicals the input resistance of the cell was so low as to be unmeasurable, because the applied current leaked through gap junctions. After injection, however, the input resistance was significantly increased. 3. After the injection dye-coupling between horizontal cells was not observed when examined by intracellular injection of Lucifer Yellow dye, supporting the idea that high concentrations of intracellular cyclic AMP block gap junctions. 4. In this situation responses to light delivered to the receptive field centre were increased in amplitude, while responses to light delivered to the receptive field surround were greatly diminished. 5. After injection horizontal cells were readily polarized by conventional intracellular current injection. The hyperpolarizing light responses in carp and turtle luminosity-type cells (H1 cells) could be reversed by depolarizing the horizontal cells, and the reversal potentials were estimated to be about 0 mV. In addition, the resistance increase which accompanied the hyperpolarizing light responses could be detected. 6. In turtle biphasic chromaticity-type horizontal cells (H2 cells), hyperpolarizing light responses to shorter wavelengths and depolarizing ones to longer wavelengths could be reversed by depolarizing the horizontal cells. Both responses have almost the same reversal potential at about 0 mV. The membrane resistance changes associated with light responses were also detected; the resistance increased during the hyperpolarizing response, while it decreased during the depolarizing response. These observations suggest that the ionic mechanisms of both responses are probably the same, irrespective of their polarities.

Animals↗

Tetraethylammonium-sensitive apical K+ channels mediating K+ secretion by turtle colon.

1. Apical membrane K+ channels in turtle colon were identified and characterized using current fluctuation analysis. 2. Under short-circuit conditions in NaCl-Ringer solution, the power density spectrum (PDS) of the short-circuit current (Isc) sometimes exhibited a clearly discernible Lorentzian component, indicating spontaneous fluctuations produced by a population of apical ion channels. The Lorentzian component had a characteristic corner frequency (fc) which averaged 10.2 +/- 0.9 Hz (mean +/- S.E.M., n = 20). 3. The power of the spontaneous fluctuations was enhanced (So increased) by manoeuvres that depolarize the apical membrane electrical potential (Va). Discernible fluctuations were enhanced or induced by raising the serosal K+ concentration ([K+]s = 50-115 mM, Na+ replacement), by clamping the transepithelial potential (Vt) to serosa-positive values, or by blocking basolateral K+ channels with Ba2+. 4. Mucosal amiloride (100 microM) attenuated the spontaneous fluctuations observed in NaCl-Ringer solution but had no effect in the presence of serosal high K+, indicating that amiloride did not block the K(+)-permeable channels but these channels resided in the same cells as the amiloride-sensitive Na+ channels. 5. Raising the mucosal K+ concentration attenuated spontaneous fluctuations. 6. In the presence of serosal high K+ and mucosal amiloride, the spontaneous fluctuations were often accompanied by a reversed Isc consistent with K+ secretion. These conditions were used to test the effects of putative channel blockers. 7. Mucosal Ba2+ and tetraethylammonium (TEA+) were effective inhibitors of the spontaneous fluctuations and the reversed Isc. At a concentration of 10 mM, TEA+ was maximally effective but the TEA+ analogues tetramethylammonium (TMA+) and tetrapropylammonium (TPrA+) were much less effective. Mucosal Rb+ or Cs+ did not inhibit at a concentration of 10 mM. 8. Mucosal lidocaine (200 microM), quinidine (200 microM), or diphenylamine-2-carboxylate (DPC, 1 mM) had little or no effect on the spontaneous fluctuations and reversed Isc. Quinine (100 microM), 4-aminopyridine (1 mM), and apamin (100 nM) were also without effect. 9. Mucosal TEA+ (10 mM) abolished the active secretory K+ flux measured in the presence of serosa-positive transepithelial potentials. 10. These experiments identified a population of TEA(+)-sensitive, apical K+ channels which mediate active K+ secretion in turtle colon. Sensitivity to external TEA+ distinguishes these channels from basolateral K+ channels in turtle colon and demonstrates similarity to apical K+ channels in mammalian colon.

Amiloride↗

Calcium spikes and calcium plateaux evoked by differential polarization in dendrites of turtle motoneurones in vitro.

1. The ability of dendrites in turtle motoneurones to support calcium spikes and calcium plateaux was investigated using differential polarization by applied electric fields. 2. Electric fields were generated by passing current through transverse slices of the turtle spinal cord between two plate electrodes. The linear extracellular voltage gradient generated by the field implied that the tissue was ohmic and homogeneous. 3. The transmembrane potential at the cell body of motoneurones was measured as the voltage difference between an intracellular and an extracellular microelectrode. 4. In normal medium an applied field induced synaptic activity as well as intrinsic polarization of motoneurones. Synaptic activity was suppressed by tetrodotoxin (TTX, 1 microM). 5. In the presence of TTX and tetraethylammonium (TEA, 1-5 mM), applied fields evoked multicomponent Ca2+ spikes in both the soma-hyperpolarizing and soma-depolarizing direction of the field. The different components of Ca2+ spikes were discrete and additive. High amplitude components had higher threshold and faster time course and were followed by larger after-hyperpolarizations, than low amplitude components. The frequency of field-evoked regenerative responses was relatively insensitive to somatic bias current. 6. TTX-resistant Ca(2+)-mediated plateau potentials promoted by apamin were evoked by differential polarization in both the soma-depolarizing and soma-hyperpolarizing direction. 7. It is concluded that Ca2+ channels responsible for Ca2+ spikes and Ca2+ plateaux are present in dendrites of spinal motoneurones of the turtle.

Animals↗

Role of synaptic inhibition in turtle respiratory rhythm generation.

In vitro brainstem and brainstem-spinal cord preparations were used to determine the role of synaptic inhibition in respiratory rhythm generation in adult turtles. Bath application of bicuculline (a GABA(A) receptor antagonist) to brainstems increased hypoglossal burst frequency and amplitude, with peak discharge shifted towards the burst onset. Strychnine (a glycine receptor antagonist) increased amplitude and frequency, and decreased burst duration, but only at relatively high concentrations (10-100 microM). Rhythmic activity persisted during combined bicuculline and strychnine application (50 microM each) with increased amplitude and frequency, decreased burst duration, and a rapid onset-decrementing burst pattern. The bicuculline-strychnine rhythm frequency decreased during mu-opioid receptor activation or decreased bath P(C)(O(2)). Synaptic inhibition blockade in the brainstem of brainstem-spinal cord preparations increased burst amplitude in spinal expiratory (pectoralis) nerves and nearly abolished spinal inspiratory activity (serratus nerves), suggesting that medullary expiratory motoneurons were mainly active. Under conditions of synaptic inhibition blockade in vitro, the turtle respiratory network was able to produce a rhythm that was sensitive to characteristic respiratory stimuli, perhaps via an expiratory (rather than inspiratory) pacemaker-driven mechanism. Thus, these data indicate that the adult turtle respiratory rhythm generator has the potential to operate in a pacemaker-driven manner.

Animals↗

Evaporative water loss in box turtles: effects of rostral brainstem and other temperatures.

Box turtles were implanted with thermodes astride the preoptic tissue of the brainstem. The rate of evaporative water loss could be transiently increased by heating the rostral brainstem. Heating tissue in the anterior hypothalamus affected evaporative water loss only a high ambient temperatures. The magnitude of the response was proportional both to the change in hypothalamic temperature and to the ambient temperature with which the turtle was in equilibrium. The major fuction of a high rate of evaporative water loss in turtles is probably to protect the brain from overheating during thermal stress.

Animals↗

Eradication of Arizona hinshawii from artificially infected turtle eggs.

Turtle eggs, 24 h old, were infected with Arizona hinshawii and treated 48 h later with gentamicin sulfate (Garasol; Shering Corp., Allantown, N.J.) by pressure differential egg dip treatment to ascertain the concentration of this reagent required to eradicate this pathogen from eggs. Infected eggs treated with 1,000 or 1,500 micrograms of gentamicin per ml of dip solution eliminated detectable A. hinshawii from eggs as determined by testing shells and embryo-yolk homogenates of 12-day-old eggs and the gastrointestinal tracts, kidneys, livers and gall bladders, and yolks of 50-day-old embryos. Treated eggs produced hatchlings which did not excrete detectable A. hinshawii at 72 h or 30 days after hatching, nor was this organism recovered from the visceral organs of these hatchlings when necropsied 30 days after hatching. Bacteriological assays on infected nontreated eggs showed that greater than 70% of the eggs harbored A. hinshawii, and eggs in this group produced hatchlings which actively excreted and harbored A. hinshawii. Eggs not infected or treated also produced turtles which excreted and systemically carried A. hinshawii and Salmonella spp. though not at the same level as did the turtles produced from infected, nontreated eggs.

Animals↗

Isolation of Campylobacter fetus from a pet turtle.

During the course of a Salmonella agona case investigation, Campylobacter fetus was isolated from a pet turtle. This is the first reported isolation of C. fetus from a turtle and suggests that turtles, in addition to being reservoirs for Salmonella species, may also be reservoirs for C. fetus.

Animals↗

Cutaneous hyalohyphomycosis caused by Fusarium solani in a loggerhead sea turtle (Caretta caretta L.).

Fusarium solani was reported as the agent of a cutaneous infection in an injured sea turtle collected in the Mediterranean Sea. The turtle was treated with both a topical 10% solution of iodine in alcohol and ketoconazole. The source of the causal agent was traced to the sand in the tank in which the turtle was maintained. The strain was only sensitive in vitro to amphotericin B and was resistant to 5-fluorocytosine, fluconazole, itraconazole, and ketoconazole.

Administration, Topical↗

Identification and expression of immunogenic proteins of a disease-associated marine turtle herpesvirus.

Herpesviruses are associated with several diseases of marine turtles, including lung-eye-trachea disease (LETD) and fibropapillomatosis. Two approaches were used to identify immunodominant antigens of LETV, the LETD-associated herpesvirus. The first approach targeted glycoprotein B, which is known to be immunogenic and neutralizing in other species. The second strategy identified LETV proteins recognized on Western blots by antibodies in immune green turtle plasma. A 38-kDa protein was resolved by two-dimensional gel electrophoresis, sequenced, and identified as a scaffolding protein encoded by the overlapping open reading frames of UL26 and UL26.5. Glycoprotein B and the scaffolding protein were cloned and expressed in Escherichia coli. The expressed proteins were recognized on Western blots by antibodies in immune green turtle plasma. Phylogenetic studies based on UL26, DNA polymerase, and glycoprotein B revealed that LETV clusters with the alphaherpesviruses.

Alphaherpesvirinae↗

Vasoactive intestinal peptide stimulates alkali excretion in turtle urinary bladder.

The turtle urinary bladder possesses an active transport mechanism for the electrogenic secretion of alkali. This process is independent of exogenous Cl and Na, induced by cyclic AMP (cAMP), and potentiated in bladders from NaHCO3-loaded (alkalotic) turtles. In the present study, it is shown that the serosal addition of vasoactive intestinal peptide (VIP) induces rapidly developing parallel increases in alkali secretion and in the short-circuiting current carried by this secretion. The VIP-induced increment in alkali secretion is greater in the presence than in the absence of an exogenously added phosphodiesterase inhibitor. Additions of a cAMP analog subsequent to the VIP-induced alkali secretion fail to induce any further increase in alkalinization. These results provide evidence for the action of VIP as a hormonal up regulator of alkali excretion in the turtle urinary bladder.

1-Methyl-3-isobutylxanthine↗