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PubMed1999

The ecological role of the prehensile tail in white-faced capuchins (Cebus capucinus).

Prehensile tails appear to have evolved at least twice in platyrrhine evolution. In the atelines, the tail is relatively long and possesses a bare area on the distal part of its ventral surface that is covered with der-matoglyphs and richly innervated with Meissner's corpuscles. In contrast, the prehensile tail of Cebus is relatively short, fully haired, and lacks specialized tactile receptors. Little is currently known regarding tail function in capuchins, and whether their prehensile tail serves a greater role in feeding or traveling. In this paper we examine patterns of positional behavior, substrate preference, and tail use in wild white-faced capuchins (Cebus capucinus) inhabiting a wet tropical forest in northeastern Costa Rica. Observational data were collected over the course of 3 months on adult capuchins using an instantaneous focal animal time sampling technique. Differences in the frequency and context of tail use, and the estimated amount of weight support provided by the tail relative to other appendages during feeding/foraging and traveling were used as measures of the ecological role of this specialized organ in capuchin positional behavior. During travel, quadrupedal walking, leaping, and climbing dominated the capuchin positional repertoire. The capuchin tail provided support in only 13.3% of travel and was principally employed during below branch locomotor activities. In contrast, tail-assisted postures accounted for 40.6% of all feeding and foraging records and occurred primarily in two contexts. The tail was used to suspend the individual below a branch while feeding, as well as to provide leverage and weight support in above-branch postures associated with the extraction of prey from difficult to search substrates. A comparison of tail use in Cebus, with published data on the atelines indicates that both taxa possess a grasping tail that is capable of supporting the animal's full body weight. In capuchins and howling monkeys, the tail appears to be used more frequently and serves a greater weight-bearing role during feeding than during traveling. In Ateles, and possibly Brachyteles, and Lagothrix, however, the prehensile tail serves a dual role in both feeding and forelimb suspensory locomotion. Additional relationships between white-faced capuchin feeding, positional behavior, extractive foraging techniques, and prehensile tail use are discussed.

Animals↗
PubMed2005

Partial tail loss has no severe effects on energy stores and locomotor performance in a lacertid lizard, Takydromus septentrionalis.

Many species of lizards use caudal autotomy as a defense strategy to avoid predation, but tail loss entails costs. These topics were studied experimentally in the northern grass lizard, Takydromus septentrionalis. We measured lipids in the three-tail segments removed from each of the 20 experimental lizards (adult females) initially having intact tails to evaluate the effect of tail loss on energy stores; we obtained data on locomotor performance (sprint speed, the maximal length traveled without stopping and the number of stops in the racetrack) for these lizards before and after the tail-removing treatments to evaluate the effect of tail loss on locomotor performance. An independent sample of 20 adult females that retained intact tails was measured for locomotor performance to serve as controls for successive measurements taken for the experimental lizards. The lipids stored in the removed tail was positively correlated with tailbase width when holding the tail length constant, indicating that thicker tails contained more lipids than did thinner tails of the same overall length. Most of the lipids stored in the tail were concentrated in the proximal portion of the tail. Locomotor performance was almost unaffected by tail loss until at least more than 71% of the tail (in length) was lost. Our data show that partial tail loss due to predatory encounters or other factors may not severely affect energy stores and locomotor performance in T. septentrionalis.

Animals↗
PubMed2004

Limits on the evolution of tail ornamentation in birds.

In birds, elongated tails are one of the most common and most studied ornaments. However, the tail also has an aerodynamic function, playing a role in turning and slow flight. If a tail is to function as an ornament, then there will be an inevitable conflict between the aerodynamic role and the signaling role. Aerodynamic theory has developed to the point where it is possible to predict the aerodynamic and mechanical consequences of ornamental tails of different sizes and shapes. Tail elongation will influence many different mechanical and aerodynamic parameters. For at least some and possibly all of these parameters, there will be limits that are placed by the bird's anatomy, morphology, or physiology on the extent to which the effect of tail elongation could be tolerated. For example, if a particular tail morphology meant that the power required to fly exceeded the power available from the flight muscles, then the bird would obviously be unable to fly with such a tail. To examine whether these considerations could limit the development of ornamental tails, the effect of long tails of different shapes was examined on three parameters: static balance, lift-to-drag ratio, and the cost of flight. All three of these parameters were found to limit the range of possible tail morphologies that could be developed by birds. These limits were most acute for small birds, which may not be able to operate with a long tail of any shape. Slightly larger birds would be able to develop elongated streamers and forked tails but not pintails or wedge-shaped tails. Medium to large birds are less constrained and could develop a much wider range of tails than small birds, but there will always be limits to the sizes of tail ornament that could be developed. Thus the physical consequences of ornamentation on ecology and behavior are likely to be responsible for some of the patterns of ornamentation observed in nature.

Animals↗
PubMed1993

Rat tail flick reflex: magnitude measurement of stimulus-response function, suppression by morphine and habituation.

1. To quantitatively investigate a nocifensive behavioral response, we developed a method to measure the magnitude of the rat's tail flick reflex and its modulation. A radial array of force transducers measured forces of tail flicks (in rostral, horizontal, and vertical planes) elicited by graded noxious radiant thermal stimulation of the conscious rat's tail, from which the overall movement vector was calculated. 2. The rostrally directed component of tail flicks was always larger than dorsal or horizontal components; the latter was usually in a preferred (left or right) direction regardless of which side of the tail was heated. Tail flick force vectors increased from 40 to 46-52 degrees C and then leveled off. Stimulus-response functions were reproducible within and across rats and were fitted by second-order polynomial functions, whose correlation coefficients were similar when the left or right side of the tail was stimulated in separate sessions (r2 = 0.408 and 0.451, respectively). The inverse latency of tail flicks also increased with temperature in a manner fitted by a second-order polynomial (r2 = 0.707, 0.553 for left and right side, respectively). 3. Systemic administration of morphine (1 or 2 mg/kg ip) usually suppressed tail flicks in an all-or-none manner; i.e., flicks at all stimulus temperatures were either totally abolished (n = 7) or unaffected (n = 5) after morphine. In three rats, 1 mg/kg morphine suppressed tail flick magnitude subtotally, reducing the slope of the linear portion of the stimulus-response function. Morphine effects were reversed by the opiate antagonist naloxone. 4. Tail flick magnitude decreased over repeated trials of 44 degrees C heat stimuli delivered to one tail site, recovered after a 15-min rest period, and decremented more quickly with subsequent stimulus repetition. The decrement was less at long (2 or 4 min) than at short (1 min) interstimulus intervals, and high (50 degrees C) than at low (44 degrees C) stimulus intensities. The reflex decrement transferred to a nearby stimulus site in some rats, and was "dishabituated" after a noxious tail pinch. These observations are consistent with habituation of the tail flick reflex. 5. This method, therefore, provides a quantitative and reproducible measure of tail flick reflex magnitude that is sensitive to morphine. The underlying neural circuitry of the tail flick reflex is discussed in relation to limb withdrawal reflexes.

Afferent Pathways↗
PubMed1983

Slow components of potassium tail currents in rat skeletal muscle.

The kinetics of potassium tail currents have been studied in the omohyoid muscle of the rat using the three-microelectrode voltage-clamp technique. The currents were elicited by a two-pulse protocol in which a conditioning pulse to open channels was followed by a test step to varying levels. The tail currents reversed at a single well-defined potential (VK). At hyperpolarized test potentials (-100 mV and below), tail currents were inward and exhibited two clearly distinguishable phases of decay, a fast tail with a time constant of 2-3 ms and a slow tail with a time constant of approximately 150 ms. At depolarized potentials (-60 mV and above), tail currents were outward and did not show two such easily separable phases of decay, although a slow kinetic component was present. The slow kinetic phase of outward tail currents appeared to be functionally distinct from the slow inward tail since the channels responsible for the latter did not allow significant outward current. Substitution of Rb for extracellular K abolished current through the anomalous (inward-going) rectifier and at the same time eliminated the slow inward tail, which suggests that the slow inward tail current flows through anomalous rectifier channels. The amplitude of the slow inward tail was increased and VK was shifted in the depolarizing direction by longer conditioning pulses. The shift in VK implies that during outward currents potassium accumulates in a restricted extracellular space, and it is suggested that this excess K causes the slow inward tail by increasing the inward current through the anomalous rectifier. By this hypothesis, the tail current slowly decays as K diffuses from the restricted space. Consistent with such a hypothesis, the decay of the slow inward tail was not strongly affected by changing temperature. It is concluded that a single delayed K channel is present in the omohyoid. Substitution of Rb for K has little effect on the magnitude or time course of outward current tails, but reduces the magnitude and slows the decay of the fast component of inward tails. Both effects are consistent with a mechanism proposed for squid giant axon (Swenson and Armstrong, 1981): that (a) the delayed potassium channel cannot close while Rb is inside it, and (b) that Rb remains in the channel longer than K.

Animals↗
PubMed2004

Use of the tail moment of the lymphocytes to evaluate DNA damage in human biomonitoring studies.

The Comet assay has gained increasing popularity for use in human biomonitoring or epidemiologic studies; however, one of the shortcomings of the Comet assay is a lack of agreement on a single appropriate Comet parameter that is capable of adequately describing observed DNA damages. Among the tail parameters of Comet features, the most frequently used are the tail moments (both the Olive tail moment and the extent tail moment), the tail DNA, and the tail length. Some studies comparing Comet parameters have been found in cell toxicity research, but there are few comparative studies that use human biomonitoring or epidemiologic data. In this study, we evaluate those four tail parameters in both high and low DNA damaged cells with the use of epidemiologic data. To do this, a new graphical approach, the so-called quantile dispersion graphs (QDGs) are used. In a comparison of an exposed group and a control group, either the tail moment or tail DNA is preferable to the tail length. With respect to providing smaller variability in quantiles for the amount of DNA damage, however, the tail moment is the preferred parameter for both groups. Moreover, the tail moment provides the most stable estimates for DNA damage because it has a larger degree of uniformity in quantile dispersions. To study high degrees of damage from toxic exposure using B cells or G cells, however, the tail DNA showed more significant discrepancies than the other parameters, in terms of both the mean differences and the graphical differences between the two groups. In view of this result, it is suggested that both the tail moment and the tail DNA be presented as tail parameters in human biomonitoring studies.

Adult↗
PubMed1985

Irreversible binding to the receptor of bacteriophages T5 and BF23 does not occur with the tip of the tail.

Treatment of purified tails of bacteriophage T5 with 0.05% sodium dodecyl sulfate specifically removed pb2, a protein of 108,000 molecular weight (108K), from the tail. Although these tails were devoid of the single straight tail fiber, they still inhibited adsorption of T5 to Escherichia coli cells. Reconstitution of these tails with pb2 increased the efficiency of inhibition of T5 adsorption. Treatment of tails with 0.1% sodium dodecyl sulfate removed, in addition to pb2, a protein of 67K from phage T5 and one of 60K from phage BF23. These tails failed to inhibit phage adsorption, and no reconstitution was achieved. Reconstitution of T5 tails with pb2 from BF23, and of BF23 tails with pb2 from T5, did not alter the host receptor specificity of the tails. Binding of untreated T5 tails to small FhuA receptor particles revealed that binding occurred with the conical part of the tail and that pb2 was most likely released from the tail upon binding. From these results and from recent observations with T5-BF23 hybrid phages (K.J. Heller, Virology 139:11-21, 1984), we conclude that the receptor-binding proteins of T5 and BF23 are the 67K and 60K proteins, respectively, and that they are not located at the tip of the tail but rather at or near the site where the straight tail fiber is attached to the conical part of the tail.

Coliphages↗
PubMed1995

Comparative and functional myology of the prehensile tail in New World monkeys.

The caudal myology of prehensile-tailed monkeys (Cebus apella, Alouatta palliata, Alouatta seniculus, Lagothrix lagotricha, and Ateles paniscus) and nonprehensile-tailed primates (Eulemur fulvus, Aotus trivirgatus, Callithrix jacchus, Pithecia pithecia, Saimiri sciureus, Macaca fascicularis, and Cercopithecus aethiops) was examined and compared in order to identify muscular differences that correlate with osteological features diagnostic of tail prehensility. In addition, electrophysiological stimulation was carried out on different segments of the intertransversarii caudae muscle of an adult spider monkey (Ateles geoffroyi) to assess their action on the prehensile tail. Several important muscular differences characterize the prehensile tail of New World monkeys compared to the nonprehensile tail of other primates. In atelines and Cebus, the mass of extensor caudae lateralis and flexor caudae longus muscles is more uniform along the tail, and their long tendons cross a small number of vertebrae before insertion. Also, prehensile-tailed monkeys, especially atelines, are characterized by well-developed flexor and intertransversarii caudae muscles compared to nonprehensile-tailed primates. Finally, Ateles possesses a bulkier abductor caudae medialis and a more cranial origin for the first segment of intertransversarii caudae than do other prehensile-tailed platyrrhines. These myological differences between nonprehensile-tailed and prehensile-tailed primates, and among prehensile-tailed monkeys, agree with published osteological and behavioral data. Caudal myological similarities and differences found in Cebus and atelines, combined with tail-use data from the literature, support the hypothesis that prehensile tails evolved in parallel in Cebus and atelines.

Animals↗
PubMed1993

Morphological evidence for secondary formation of the tail gut in the rat embryo.

The secondary body formation is a developmental mechanism occurring in the caudal part of the embryo in which embryonic structures arise from a mass of mesenchymal cells without previous formation of germ layers. The formation of the tail gut by this mechanism was investigated on transverse serial semithin and ultrathin sections of 12-, 13-, 14- and 15-day rat embryo tails. The tail gut, together with the tail portion of the notochord, originates from an axial mass of condensed mesenchymal cells named tail cord. Formation of the tail gut involves the appearance of large intercellular junctions among tail cord cells, and rearrangement of these cells around a newly formed lumen. Mesenchymal characteristics of these cells are gradually lost, and they simultaneously acquire the morphology of epithelial cells. Some cells of the tail cord, located ventral to the tail gut, do not participate in the tail gut formation and form a separate mass of cells without any definitive morphogenetic fate. This surplus group of cells is first evident in 12-day embryos, and it increases in mass during the following 3 days. In 15-day embryos, after the tail gut has completely disappeared, the surplus cells represent all that remains of the tail cord. The mesenchymal-epithelial transformation of the tail cord cells into the cells of the tail gut, and the appearance of the surplus cells, could be considered as the main morphological arguments for the secondary formation of the tail gut.

Animals↗
PubMed2006

Energetic and locomotor costs of tail loss in the Chinese skink, Eumeces chinensis.

Caudal autotomy is a defense mechanism used by numerous lizards to evade predators, but this entails costs. We collected 294 adult Chinese skinks (Eumeces chinensis) from a population in Lishui (eastern China) to evaluate energetic and locomotor costs of tail loss. Of the 294 skinks, 214 (c. 73%) had previously experienced caudal autotomy. Neither the proportion of individuals with regenerated tails nor the frequency distribution of locations of the tail break differed between sexes. We successively removed four tail segments from each of the 20 experimental skinks (adult males) initially having intact tails. Lipid content in each removed tail segment was measured, and locomotor performance (sprint speed, the maximal length traveled without stopping and the number of stops in the racetrack) was measured for each skink before and after each tail-removing treatment. Another independent sample of 20 adult males with intact tails was measured for locomotor performance to serve as controls for successive measurements taken for the experimental lizards. Caudal lipids were disproportionately stored along the length of the tail, with most lipids being aggregated in its proximal portion. Tail loss significantly affected sprint speed, but not the maximal length of, or the number of stops during the sprint. However, the adverse influence of tail loss on sprint speed was not significant until more than 51% of the tail (in length) was lost. Our data show that partial tail loss due to predatory encounters or other factors may not severely affect energy stores or locomotor performance in E. chinensis. As tail breaks occurred more frequently in the proximal portion of the tail in skinks collected from the field, we conclude that caudal autotomy occurring in nature often incurs substantial energetic and locomotor costs in E. chinensis.

Animals↗
PubMed2000

Influence of tail shape on tadpole swimming performance.

Many tadpoles respond to insect predators by developing deeper, and sometimes longer, tails. It has been assumed that the larger tail enhances aspects of swimming performance, because deep-tailed tadpoles survive well when confronted with hunting predators. We tested this hypothesis using both naturally occurring and surgically created variation in tail morphology of Hyla versicolor tadpoles. We measured swimming performance (maximum speed, time to reach a 2.5 cm radius, and angle of escape) and morphology (size and shape of the body and tail) in 288 tadpoles, of which half possessed the predator-induced morphology and the other half were from predator-free ponds. Large tadpoles swam faster than small ones, and shape was significantly correlated with size-corrected swimming performance. The fastest tadpoles had relatively shallow bodies and tail fins, and short tails; there was no difference in swimming performance between predator-induced and no-predator tadpoles. We performed an experiment to create independent variation in tail depth and length by surgically manipulating tail shape in 270 tadpoles. Three tail-length treatments reduced the length of the tail fin by 21 %, 34 % and 55 %; three tail-depth treatments reduced the maximum depth of the tail fin by 11 %, 34 % and 59 %; two additional treatments controlled for the effects of anaesthesia and surgery. The angle of escape was unaffected by surgery. Maximum speed and minimum escape time were both significantly impaired by the high-removal treatments, but showed no evidence of decline until 30 % of the tail (length or depth) was removed. These results suggest that the relatively deep tails in predator-induced tadpoles (approximately 10 % deeper than in no-predator tadpoles) do not improve performance in burst swimming. Thus, predator-induced tadpoles are less vulnerable to predation for reasons other than enhanced swimming performance.

Animals↗
PubMed2002

Function of the heterocercal tail in sharks: quantitative wake dynamics during steady horizontal swimming and vertical maneuvering.

The function of the heterocercal tail in sharks has long been debated in the literature. Previous kinematic data have supported the classical theory which proposes that the beating of the heterocercal caudal fin during steady horizontal locomotion pushes posteroventrally on the water, generating a reactive force directed anterodorsally and causing rotation around the center of mass. An alternative model suggests that the heterocercal shark tail functions to direct reaction forces through the center of mass. In this paper, we quantify the function of the tail in two species of shark and compare shark tail function with previous hydrodynamic data on the heterocercal tail of sturgeon Acipenser transmontanus. To address the two models of shark heterocercal tail function, we applied the technique of digital particle image velocimetry (DPIV) to quantify the wake of two species of shark swimming in a flow tank. Both steady horizontal locomotion and vertical maneuvering were analyzed. We used DPIV with both horizontal and vertical light sheet orientations to quantify patterns of wake velocity and vorticity behind the heterocercal tail of leopard sharks (Triakis semifasciata) and bamboo sharks (Chiloscyllium punctatum) swimming at 1.0Ls(-1), where L is total body length. Two synchronized high-speed video cameras allowed simultaneous measurement of shark body position and wake structure. We measured the orientation of tail vortices shed into the wake and the orientation of the central jet through the core of these vortices relative to body orientation. Analysis of flow geometry indicates that the tail of both leopard and bamboo shark generates strongly tilted vortex rings with a mean jet angle of approximately 30 degrees below horizontal during steady horizontal swimming. The corresponding angle of the reaction force is much greater than body angle (mean 11 degrees ) and the angle of the path of motion of the center of mass (mean approximately 0 degrees ), thus strongly supporting the classical model of heterocercal tail function for steady horizontal locomotion. Vortex jet angle varies significantly with body angle changes during vertical maneuvering, but sharks show no evidence of active reorientation of jet angle relative to body angle, as was seen in a previous study on the function of sturgeon tail. Vortex jet orientation is significantly more inclined than the relatively horizontal jet generated by sturgeon tail vortex rings, demonstrating substantial differences in function in the heterocercal tails of sharks and sturgeon. We present a summary of forces on a swimming shark integrating data obtained here on the tail with previous data on pectoral fin and body function. Body orientation plays a critical role in the overall force balance and compensates for torques generated by the tail. The pectoral fins do not generate lift during steady horizontal locomotion, but play an important hydrodynamic role during vertical maneuvering.

Animals↗
PubMed1998

Role of differential cell proliferation in the tail bud in aberrant mouse neurulation.

In the mouse mutant curly tail, the phenotypes spina bifida and curled tail result from a delay in closure of the posterior neuropore (PNP). At the developmental stage when this delay can first be recognized, the caudal region of the embryo demonstrates a transiently enhanced curvature of the body axis which likely inhibits elevation, convergence, and fusion of the neural folds. The enhanced curvature is thought to be the result of a decreased proliferation in the ventrally located gut endoderm and notochord, together with a normal proliferation of the overlying neuroepithelium of the PNP. However, the proliferation defect and the enhanced curvature were originally demonstrated at the same developmental stage, while it is expected that reduced proliferation should precede enhanced curvature and delayed PNP closure. The caudal region originates from the tail bud and we therefore propose that the enhanced curvature is induced by a disturbed dorso-ventral proliferation pattern in the tail bud. Using flow cytometry, proliferation patterns were determined separately for the dorsal and ventral halves of the tail bud of curly tail and of control embryos as well as of recombinant embryos having the curly tail phenotype with a genetic background which is matched to the BALB/c control strain. In general, it appeared that about half of the cell cycle duration in tail bud cells was occupied by S phase, about 40% by G0/G1 and the rest by G2/M. For the control embryos, no dorso-ventral differences in relative phase duration were demonstrated. However, curly tail and recombinant embryos at the 21-25 somite stage, prior to the onset of enhanced curvature, exhibited ventrally a higher proportion of G0/G1 phase cells than dorsally, and a complementary relationship for S phase cells. We interpret these observations as indicating a prolonged G1 phase at the ventral side of the tail bud, resulting in a prolongation of the cell cycle and thus a decreased proliferation. In 26-30 somite stage embryos, prior to the normalization of curvature in curly tail embryos, the dorso-ventral proliferation balance was re-established. We conclude that a reduced proliferation in the ventral part of the tail bud of the curly tail embryo precedes both the onset of enhanced curvature and the previously observed reduction in proliferation of the hindgut and notochord, and is a likely candidate for an early event in the pathogenetic sequence leading to the curly tail phenotype.

Animals↗
PubMed1982

Antipyrine and acetaminophen kinetics in the rat: comparison of data based on blood samples from the cut tail and a cannulated femoral artery.

Antipyrine and acetaminophen kinetics were determined from concentration data obtained by simultaneous blood sampling from the cut end of the tail and a cannulated femoral artery in the rat. Significant differences in concentrations and kinetics for both drugs were found by comparison of the two sampling sites. The hypothesis that the differences were due to a low tail blood flow was tested. The tail blood flow was measured with a microsphere technique, and tail antipyrine concentrations were calculated from the relationship between arterial antipyrine concentration, tail flow, and time for comparison with the observed antipyrine concentrations. Mean blood flow of the rat tail was 0.02 ml/min/ml tail tissue at 22 degrees, which was 8.8 and 0.9% of the liver and kidney flow, respectively. Tail flow increased more than twofold by elevation of the tail temperature to 37 degrees. The calculated tail antipyrine concentration versus time curve showed a very close correspondence to the observed antipyrine tail concentration versus time curves. The results show that tail flow is a major determinant of antipyrine tail concentration in the rat. Kinetic data based on blood samples from the cut end of the tail, therefore, should be interpreted with caution.

Acetaminophen↗
PubMed2004

Morphological features of tail bud development in truncate mouse mutants.

A key malformation in the homozygous truncate mouse mutants is a partial lack of the notochord in the embryo tail. In order to analyze if tail bud development was affected by the truncate (tc) mutation, serial semithin sections of tails of the homozygous mutant embryos were compared to the wild-type controls. In the wild-type embryos morphologically uniform mesenchyme of the tail bud was continuous via the medullary cord to the secondary neural tube, and via the tail cord to the notochord and the gut. In truncate embryos the tail cord was not continuous to the notochord, but to the additional lumen of the tail gut resulting in tail gut duplication. Toward the base of the tail two tail guts subsequently fused together or the additional one disappeared. If present in the tip of the tail, the notochord in truncate embryos ended near the ventral border of the secondary neural tube. The rest of the tail notochord was fragmented and the posterior ends of the fragments were frequently adjacent or even continuous to the neural tube. We suggest that the improper regionalization of the tail bud, where notochord is associated with the neural tube rather than with the tail gut, is related to the subsequent segmental lack of the notochord in truncate mutants.

Animals↗
PubMed1999

A developmental pathway controlling outgrowth of the Xenopus tail bud.

We have developed a new assay to identify factors promoting formation and outgrowth of the tail bud. A piece of animal cap filled with the test mRNAs is grafted into the posterior region of the neural plate of a host embryo. With this assay we show that expression of a constitutively active Notch (Notch ICD) in the posterior neural plate is sufficient to produce an ectopic tail consisting of neural tube and fin. The ectopic tails express the evenskipped homologue Xhox3, a marker for the distal tail tip. Xhox3 will also induce formation of an ectopic tail in our assay. We show that an antimorphic version of Xhox3, Xhox3VP16, will prevent tail formation by Notch ICD, showing that Xhox3 is downstream of Notch signalling. An inducible version of this reagent, Xhox3VP16GR, specifically blocks tail formation when induced in tailbud stage embryos, comfirming the importance of Xhox3 for tail bud outgrowth in normal development. Grafts containing Notch ICD will only form tails if placed in the posterior part of the neural plate. However, if Xwnt3a is also present in the grafts they can form tails at any anteroposterior level. Since Xwnt3a expression is localised appropriately in the posterior at the time of tail bud formation it is likely to be responsible for restricting tail forming competence to the posterior neural plate in our assay. Combined expression of Xwnt3a and active Notch in animal cap explants is sufficient to induce Xhox3, provoke elongation and form neural tubes. Conservation of gene expression in the tail bud of other vertebrates suggests that this pathway may describe a general mechanism controlling tail outgrowth and secondary neurulation.

Animals↗
PubMed2004

Characterization and availability of cyanide in solid mine tailings from gold extraction plants.

The aim of this study was to investigate the availability and fate of cyanide in gold mill solid tailings. For this purpose, aged (6-9 years) and recently discharged (3 months) tailings were sampled at various depths from two gold mining sites in Quebec (Canada). A physicochemical characterization of the tailings along with a bacterial enumeration was performed and batch-leaching tests with water and caustic solution were conducted to assess the soluble cyanide fraction. Following the standard acid reflux/distillation method, the total cyanide concentration (CN(T)) in fresh tailings was higher (average of 19.5 +/- 2.0 compared to 3.2 +/- 0.7 mg/kg) and the pH more alkaline (10.6 +/- 0.1 compared to 7.6 +/- 0.2) compared to aged ones. In aged tailings, the enumeration of total heterotrophic (10(4)-10(6) cfu/g) and cyanide-resistant bacteria (10(2)-10(5) cfu/g) showed a significant indigenous microflora, but no growth on agar plates was detected in fresh tailings, suggesting an evolution and a gradual acclimatization of bacterial populations with weathering. Elevated concentrations of CN(T), weak acid dissociable cyanide (CN(WAD)), cyanate (CNO-), and thiocyanate (SCN-) were measured in the supernatant solution of the fresh tailings samples collected in-situ, highlighting their reactivity, whereas these species were not detectable in aged tailings. Accordingly, when batch-leaching tests were performed with fresh samples, 68-72% of the total cyanide was released into aqueous solution with more than 20% being CN(WAD). Again, CN(T) and CN(WAD) were not detectable during leaching of aged tailings. In fresh tailings, approximately 50% of the cyanides were quantifiable with the standard acid reflux/distillation method (readily soluble cyanides, and weak to moderately strong complexes), whereas in aged tailings only 15 to 33% of the actual total cyanide content was measured by the standard method. These results stress the necessity of performing a preliminary alkaline extraction prior to total cyanide determination. In summary, this study revealed a difference in physicochemical properties, cyanide concentration and speciation, viable bacterial populations and cyanide leaching behavior between aged and fresh solid mine tailings. The findings indicate that the more reactive cyanide species initially associated with the solid tailings have naturally degraded within the mine tailings impoundment area, resulting primarily from volatilization (decrease in pH), leaching, and bacterial degradation.

Bacteria↗
PubMed2003

Speciation and characterization of arsenic in Ketza River mine tailings using X-ray absorption spectroscopy.

Ketza River mine tailings deposited underwater and those exposed near the tailings impoundment contain approximately 4 wt % As. Column-leaching tests indicated the potential for high As releases from the tailings. The tailings are composed dominantly of iron oxyhydroxides, quartz, calcite, dolomite, muscovite, ferric arsenates, and calcium-iron arsenates. Arsenopyrite and pyrite are trace constituents. Chemical compositions of iron oxyhydroxide and arsenate minerals are highly variable. The XANES spectra indicate that arsenic occurs as As(V) in tailings, but air-drying prior to analysis may have oxidized lower-valent As. The EXAFS spectra indicate As-Fe distances of 3.35-3.36 A for the exposed tailings and 3.33-3.35 A for the saturated tailings with coordination numbers of 0.96-1.11 and 0.46-0.64, respectively. The As-Ca interatomic distances ranging from 4.15 to 4.18 A and the coordination numbers of 4.12-4.58 confirm the presence of calcium-iron arsenates in the tailings. These results suggest that ferric arsenates and inner-sphere corner sharing or bidentate-binuclear attachment of arsenate tetrahedra onto iron hydroxide octahedra are the dominant form of As in the tailings. EXAFS spectra indicate that the exposed tailings are richer in arsenate minerals whereas the saturated tailings are dominated by the iron oxyhydroxides, which could help explain the greater release of As from the exposed tailings during leaching tests. It is postulated that the dissolution of ferric arsenates during flow-through experiments caused the high As releases from both types of tailings. Arsenic tied to iron oxyhydroxides as adsorbed species are considered stable; however, iron oxyhydroxides having low Fe/As molar ratios may not be as stable. Continued As releases from the tailings are likely due to dissolution of both ferric and calcium-iron arsenates and desorption of As from high-As bearing iron oxyhydroxides during aging.

Arsenates↗