Western diamondback rattlesnakes demonstrate physiological and biochemical strategies for tolerating prolonged starvation

Because of the uncertainty in food resources in nature, all animals face the possibility of imposed periods of fasting (i.e., starvation) at some point in their lives. I investigated physiological and biochemical responses to starvation that occur in a species of rattlesnake known to tolerate successfully prolonged periods of starvation in the wild. Sixteen subadult Crotalus atrox were fasted for up to 24 wk under controlled conditions simulating their active season. Snakes exhibited significant reductions in plasma glucose but increased circulating ketone bodies. Fasting snakes lost mass at a linear rate and increased their relative moisture content during the experiment. The bodies of fasting snakes demonstrated an increase in their fatty acid (FA) unsaturation index and were apparently able to "spare" essential FAs effectively from beta -oxidation. Endogenous essential and nonessential amino acids were used indiscriminately to fuel energetic requirements, suggesting that essential amino acids are not preferentially spared during starvation. The (15)N signature of excreted nitrogenous waste increased significantly, presumably as a result of shifting amino acid source pools during starvation. Because our comparative knowledge of starvation physiology contains large taxonomic gaps, particularly with respect to amphibians and reptiles, an understanding of the biological responses exhibited by these animals may offer insight into the evolution of physiological strategies animals employ to cope with the pressures of starvation.     

Rhesus Macaques (Macaca mulatta) Use Posture to Assess Level of Threat From Snakes

Once prey animals have detected predators, they must make decisions about how to respond based on a cost‐benefit analysis of their risk level. The threat sensitivity hypothesis predicts that prey animals match their response to the level of risk, with high‐risk predator encounters eliciting stronger evasive responses than low‐risk encounters. Primates are known prey of snakes, yet they vary their responses toward snakes. We predicted that primates match their response to the threat level from snakes by assessing posture, with striking postures indicating greater risk than coiled postures and coiled postures indicating greater risk than extended sinusoidal postures. We tested this prediction in a series of experimental trials in which captive rhesus macaques (Macaca mulatta) were exposed to snake models in those postures. Results supported the predictions: macaques responded more strongly to a snake model in a striking posture than in a coiled posture and more to a snake model in a coiled posture than to an extended sinusoidal snake model. We also examined responses of macaques to a partially exposed snake model to mimic the condition of incomplete information, as snakes are often occluded by vegetation. The occluded snake model evoked a response comparable to that of the striking snake. These findings support the threat sensitivity hypothesis. Rhesus macaques use the posture of snakes as a cue in threat assessment, responding more intensely as threat increases, and they also behave as if risk is elevated when their information about snakes is incomplete.     

Gastrointestinal responses to feeding in a frequently feeding colubrid snake (Natrix maura)

Ectotherm vertebrates show physiological mechanisms that reduce metabolic costs during prolonged fasting. Once feeding, these animals adopt a wide variety of metabolic responses such as changes in gastrointestinal organ masses. Up-regulatory responses after feeding have been widely explored in infrequently feeding snakes like pythons, whereas few studies have been devoted to frequently feeding snakes. In this study, we have considered the gastrointestinal responses after feeding in a frequent feeder, the viperine snake Natrix maura, in the Ebro Delta rice fields. In this habitat, viperine snakes are exposed to long periods of food deprivation due to the lack of available prey as a consequence of the man-induced rice cycle. We weighed prey items and full gut masses, and measured length of combined esophagus and stomach, and intestine of viperine snakes belonging to a wide range of sizes. Snakes concentrate foraging activity when rice fields were flooded. In this period, gut masses increased. Likewise, intestines increased in length during the feeding period, which suggests that viperine snakes probably experience a postfeeding hypertrophy of their small intestines that contributes to their larger length. Once the intestine length was corrected for the snake size, it was shown that adults present longer intestines than immature snakes, reflecting an increase in the posterior part of the body linked to the gonads development. This study contributes to explore the physiological responses to feeding in frequently feeding snakes modelled by abrupt shifts of food availability.     

Allometry and selection in a novel predator–prey system: Australian snakes and the invading cane toad

Because many organismal traits vary with body size, interactions between species can be affected by the respective body sizes of the participants. We focus on a novel predator–prey system involving an introduced, highly toxic anuran (the cane toad, Bufo marinus ) and native Australian snakes. The chance of a snake dying after ingesting a toad depends on the size of the snake and the size of the toad, and ultimately reflects the effect of four allometries: (1) physiological tolerance (the rate that physiological tolerance to toad toxin changes with snake size); (2) swallowing ability (the rate that maximal ingestible toad size (i.e. snake head size) increases with snake body size); (3) prey size (the rate that prey size taken by snakes increases with snake head size) and (4) toad toxicity (the rate that toxicity increases with toad size). We measured these allometries, and combined them to estimate the rate at which a snake's resistance changes with toad toxicity. The parotoid glands (and thus, toxicity) of toads increased disproportionately with toad size (i.e. relative to body size, larger toads were more toxic) but simultaneously, head size relative to body size (and thus, maximal ingestible prey size relative to predator size) declined with increasing body size in snakes. Thus, these two allometries tended to cancel each other out. Physiological tolerance to toxins did not vary with snake body size. The end result was that across snake species, mean adult body size did not affect vulnerability. Within species, however, smaller predators were more vulnerable, because the intraspecific rate of decrease in relative head size of snakes was steeper than the rate of increase in toxicity of toads. Thus, toad invasion may cause disproportionate mortality of juvenile snakes, and adults of the sex with smaller mean adult body sizes.     

High infection intensities,but negligible fitness costs,suggest tolerance of gastrointestinal nematodes in a tropical snake

We investigated patterns of prevalence and intensity of gastrointestinal nematode infections in a tropical natricine snake, the keelback (Tropidonophis mairii). Ninety‐eight per cent of keelbacks were infected with Tanqua anomala (Gnathostomidae), with infection intensities of up to 243 worms per snake. Infection with T. anomala caused severe inflammation of stomach mucosa and submucosa at the sites of parasite attachment and encystment. Nonetheless, we did not detect detrimental effects of nematode infection on measures of fitness among wild or captive snakes. Snakes with heavier nematode infections had higher body condition scores than less‐infected individuals. Deworming captive snakes had no measurable effect on their growth rate, body condition or locomotor performance. In combination with an earlier study on blood‐dwelling hepatozoons, our work suggests that keelbacks have a high tolerance to parasites. The ‘fast‐pace’ life history and short lifespan of these snakes may make it beneficial for them to tolerate infection, rather than expend energy on resisting parasite attack.     

MSCT在莽山烙铁头研究中的应用

利用多层螺旋计算机断层摄影(MSCT)扫描莽山烙铁头(Trimeresurus mangshanensis),通过重建显示蛇的各部分解剖结构,来探讨MSCT在保护濒危动物莽山烙铁头的应用价值。对3条莽山烙铁头进行CT扫描,扫描完毕重建出蛇的二维、三维图像,并分别显示其体表、骨骼、内脏等细节,MSCT能够对蛇的解剖、生境状况、疾病的诊断等方面进行研究和评价,也为蛇类等动物的研究提供新思路和新方法。     

Coral snake mimicry: live snakes not avoided by a mammalian predator

The occurrence of coral snake coloration among unrelated venomous and non-venomous New World snake species has often been explained in terms of warning coloration and mimicry. The idea that snake predators would avoid coral snakes in nature seems widely established and is postulated in many discussions on coral snake mimicry. However, the few workers that have tested a potential aposematic function of the conspicuous colour pattern focused exclusively on behaviour of snake predators towards coloured abstract models. Here we report on behaviour of temporarily caged, wild coatis (Nasua narica) when confronted with co-occurring live snakes, among which were two species of venomous coral snakes. Five different types of responses have been observed, ranging from avoidance to predation, yet none of the coatis avoided either of the two coral snake species or other species resembling these. As in earlier studies coatis appeared to avoid coral snake models, our findings show that results from studies with abstract snake models cannot unconditionally serve as evidence for an aposematic function of coral snake coloration.     

Feeding Strategies in Marine Snakes: An Analysis of Evolutionary, Morphological, Behavioral and Ecological Relationships

Analysis of 1,063 stomach contents from 39 species of sea snakesindicates that about one-third of the shallow, warm, marine,Indo-Australian fish families are preyed upon by sea snakes.Families of eels and gobies are taken by the greatest numbersof snake species. Most species of sea snakes feed on fish familieswhose members are relatively sedentary, dwelling along the bottom,within burrows or reef crevices. With one exception, a fishegg-eating specialization found uniquely in the Aipysurus-Emydocephaluslineage, the dietary habits of sea snakes cannot be categorizedaccording to the snakes' three phylogenetic lineages. Eels,mullet-like, rabbitfish-like and goby-like fish forms are takenby all three lineages. Two or three snake species are generalists,and numerous ones specialize on eels, goby-like fish or catfish.There are differences among sea snake species in the relationshipbetween snake neck girth and the maximum diameter of the prey;in the relationships of both snake gape measurements and fanglength, to the type of prey taken; and in the relationship ofsnake shape and body proportions to the prey selected. Severalmodes of feeding have been observed among sea snakes: feedingin nooks and crannies in the bottom or in reefs, cruising nearthe bottom, and feeding in drift lines. Analysis of percentdigestion of stomach contents and projections backward to thetimes of prey capture provides evidence for feeding periodicity.The greatest amount of diet overlap is for two species of seasnakes which do not both occur at the same locality. Where speciesdo co-occur, diet overlap index values are lower. The numbersof species present as well as their relative abundances varyamong localities as does the relative importance of generalists,eel-eaters, egg-eaters and other specialized feeders.     

Predation on snakes of Argentina: Effects of coloration and ring pattern on coral and false coral snakes

The occurrence of coral snake coloration among unrelated venomous and non‐venomous snake species has often been explained in terms of warning coloration and mimicry. In Argentina, no field tests have been conducted to confirm this mimetic association between one venomous coral species (Micrurus phyrrocryptus, Elapidae) and two non‐venomous snake species with a similar color pattern (Lystrophis pulcher and Oxyrhopus rhombifer, Colubridae). The aims of this work were to test for the possible aposematic or cryptic function of the ring pattern and coloration of coral snakes and false coral snakes from central Argentina, and to analyse whether the pattern is effective throughout the year. Predation on snakes was estimated by using non‐toxic plasticine replicas of ringed venomous and non‐venomous snakes and unbanded green snakes placed along transects in their natural habitat during the dry and rainy season. Ringed color pattern was attacked by predators despite the background color. One of the replica types was attacked more than expected during the dry season, suggesting that both shape and width of rings may influence the choice by predators. The reaction of predators towards replicas that mimic snake species with ringed patterns is independent of the geographical region, and we can conclude that mimicry characteristics are quite general when the true models are present in the area.     

Resource partitioning and interspecific competition in snakes: the search for general geographical and guild patterns

The role of interspecific competition as a key factor in the ecology of natural communities where species exploit limited resources is well established, and the study of competition dynamics in snake communities has received much attention in recent years. Twenty years ago, an acclaimed review ( Toft 1985 ) suggested that snakes were atypical among vertebrates because sympatric species usually partition the food niche. Here, I review the articles published in the last two decades with the aim of finding any general geographical or guild patterns and assessing if Toft's main conclusion is still supported by new evidence. Where appropriate, I use Monte Carlo simulations to establish whether observed patterns of niche overlap are real, or if they have occurred by chance. My study shows clear congruence in the patterns of coexistence exhibited by snake communities in different regions of the world, i.e.: (1) cold regions of the northern hemisphere (high latitudes and altitudes) exhibit low species richness and a very low, or even absent, potential for interspecific competition; (2) aquatic snakes that form communities in temperate regions generally partition the food type available and exhibit a broad similarity in habitat use with subtle differences in microhabitat use; (3) terrestrial snake communities in temperate regions are very variable in terms of their coexistence dynamics and show no evidence of generalised patterns; (4) sympatric viperids in Europe, North America and, most interestingly, tropical Asia partition the available habitat but not the prey resource; (5) competition is much stronger in tropical snake communities, and the intensity of this process fluctuates throughout the year being most intense during periods of low food availability; (6) in general, tropical snakes partition the food resource (prey type and/or prey size), but when this resource is not partitioned competitive exclusion can occur. Prey resource availability is a fundamental variable for all snake communities; this is clearly documented by studies on terrestrial snakes in Australia where, due to a relative scarcity of prey availability in the field, sympatry among species is much rarer than in other continents. I conclude that, although there are several notable exceptions, Toft's main conclusion is still supported by empirical evidence. However, I disagree with Toft's conclusion that most snakes are food specialists, and I contend that interspecific competition is important in structuring many (if not most) of the snake communities around the world.     

Can Wall Lizards Combine Chemical and Visual Cues to Discriminate Predatory from Non‐Predatory Snakes Inside Refuges?

The ability to use multiple cues in assessing predation risk is especially important to prey animals exposed to multiple predators. Wall lizards, Podarcis muralis, respond to predatory attacks from birds in the open by hiding inside rock crevices, where they may encounter saurophagous ambush smooth snakes. Lizards should avoid refuges with these snakes, but in refuges lizards can also find non‐saurophagous viperine snakes, which lizards do not need to avoid. We investigated in the laboratory whether wall lizards used different predator cues to detect and discriminate between snake species within refuges. We simulated predatory attacks in the open to lizards, and compared their refuge use, and the variation in the responses after a repeated attack, between predator‐free refuges and refuges containing visual, chemical, or visual and chemical cues of saurophagous or non‐saurophagous snakes. Time to enter a refuge was not influenced by potential risk inside the refuge. In contrast, in a successive second attack, lizards sought cover faster and tended to increase time spent hidden in the refuge. This suggests a case of predator facilitation because persistent predators in the open may force lizards to hide faster and for longer in hazardous refuges. However, after hiding, lizards spent less time in refuges with both chemical and visual cues of snakes, or with chemical cues alone, than in predator‐free refuges or in refuges with snake visual cues alone, but there were no differences in response to the two snake species. Therefore, lizards could be overestimating predation risk inside refuges. We discuss which selection pressures might explain this lack of discrimination of predatory from similar non‐predatory snakes.     

Induced defences in an endangered amphibian in response to an introduced snake predator

Introduced species have contributed significantly to the extinction of endemic species on islands. They also create new selection pressures on their prey that may result in modified life history strategies. Introduced viperine snakes (Natrix maura) have been implicated in the decline of the endemic midwife toad of Mallorca (Alytes muletensis). A comparison of A. muletensis tadpoles in natural pools with and without snakes showed that those populations subject to snake predation possessed longer tails with narrower tail fins but deeper tail muscles. Field and laboratory experiments showed that these changes in tail morphology could be induced by chemical and tactile cues from snakes. Populations of tadpoles that were subject to snake predation also displayed clear bimodal size-frequency distributions, with intermediate-sized tadpoles missing from the pools completely. Tadpoles in pools frequented by snakes developed faster in relation to their body size than those in pools without snakes. Variation in morphology between toad populations may therefore be caused by a combination of size-selective predation and tadpole plasticity. The results of this study indicate that the introduction of alien species can result in selection for induced defences, which may facilitate coexistence between predator and prey under certain conditions.     

Human overexploitation and extinction risk correlates of Chinese snakes

China is one of the countries with the richest snake biodiversity in the world. However, about one‐third of all 236 species are now considered threatened, partially due to the intense human overexploitation. Despite that, to date, no study has explicitly investigated the patterns and processes of extinction and threats of Chinese snakes, or between human exploited and unexploited snake subgroups. We addressed the following three questions: 1) which snake families proportionally include more human exploited species than expected by chance? 2) Which species traits and extrinsic factors are correlated with their extinction risk? 3) Are there differences between human exploited and unexploited species in terms of patterns and processes of extinction? We found that the family Elapidae contained a significantly higher number of exploited species. Considering eight species traits and four extrinsic factors, we performed phylogenetic correlation tests, finding that small geographic range size, large body length, oviparous reproduction, diurnal activity and high human exploitation were important in determining the extinction risk of all Chinese snakes. Moreover, human exploited snakes had a higher percentage of threatened species and large‐bodied species than unexploited snakes. Extinction risk of human exploited species was related to body length, reproduction mode and activity period, whereas that of human unexploited species were associated with geographic range size, microhabitat and annual temperature. Overall, we highlight the phylogenetic non‐random exploitation of snakes, and different factors underlying species response to human overexploitation. We suggest that conservation priority should be given to exploitation‐prone families and species with extinction‐prone traits, as identified in this study. Moreover, human exploited and unexploited species should be managed considering different strategies since their extinction risk was associated with different ecological traits. Conservation actions should also focus on preventing human threats, such as human overexploitation and habitat loss, for the effective preservation of Chinese snakes.     

Length–mass allometry in snakes

Body size and body shape are tightly related to an animal's physiology, ecology and life history, and, as such, play a major role in understanding ecological and evolutionary phenomena. Because organisms have different shapes, only a uniform proxy of size, such as mass, may be suitable for comparisons between taxa. Unfortunately, snake masses are rarely reported in the literature. On the basis of 423 species of snakes in 10 families, we developed clade‐specific equations for the estimation of snake masses from snout–vent lengths and total lengths. We found that snout–vent lengths predict masses better than total lengths. By examining the effects of phylogeny, as well as ecological and life history traits on the relationship between mass and length, we found that viviparous species are heavier than oviparous species, and diurnal species are heavier than nocturnal species. Furthermore, microhabitat preferences profoundly influence body shape: arboreal snakes are lighter than terrestrial snakes, whereas aquatic snakes are heavier than terrestrial snakes of a similar length. © 2012 The Linnean Society of London, Biological Journal of the Linnean Society, 2012, ●● , ●●–●●.     

Does rock disturbance by superb lyrebirds (Menura novaehollandiae) influence habitat selection by juvenile snakes?

Abstract: Vertebrates that destroy or disturb habitats used by other animals may influence habitat selection by sympatric taxa. In south‐east Australian forests, superb lyrebirds (Menura novaehollandiae) displace soil, leaf litter and rocks during their daily foraging activities. We investigated whether superb lyrebirds disturb small sandstone rocks that endangered broad‐headed snakes Hoplocephalus bungaroides and common small‐eyed snakes Cryptophis nigrescens use as diurnal thermoregulatory sites. To estimate the frequency of lyrebird rock disturbance, and to assess whether lyrebirds also attack small snakes, we placed 900 plasticine snake replicas under stones on rock and soil substrates along transects on three sandstone plateaux. Because juvenile snakes must select retreat sites that simultaneously allow them to thermoregulate and minimize predation risk, we quantified the thermal environments underneath stones on rock and soil substrates. During the 6‐week experiment, animals disturbed rocks on soil substrates twice as often (16.9%) as rocks lying on rock substrates (8.2%). Disturbed rocks were significantly smaller and lighter than undisturbed rocks on both substrates. Lyrebirds were the major agents of disturbance, and attacked 40% of snake models under disturbed rocks. Rocks on soil substrates conferred the greatest thermal benefits to snakes, but both species of snake avoided these microhabitats in the field. Instead, juvenile snakes selected rocks on rock substrates, and sheltered under stones that were too heavy for superb lyrebirds to disturb. By disturbing rocks over millennia, superb lyrebirds not only have shaped the physical landscape, but also may have exerted strong selection on habitat selection by sympatric snakes.     

Income breeding allows an aquatic snake Seminatrix pygaea to reproduce normally following prolonged drought-induced aestivation

1. Capital breeding is an ideal reproductive strategy for many ectotherms because it provides a disassociation between feeding and reproduction, a necessary requirement for animals that become anorexic during pregnancy. Among ectotherms, some viviparous snakes (e.g. Viperidae) exemplify the capital breeding strategy because many species (i) do not feed during pregnancy due to behavioural conflicts between reproduction and foraging, and (ii) take more than one season to accumulate sufficient energetic stores for reproduction. 2. Isolated wetlands often exhibit extreme annual fluctuations in environmental conditions with prolonged droughts periodically leaving wetlands completely dry and devoid of prey. Following droughts, however, wetlands can be extremely productive, rendering prey resources virtually unlimited for some species. 3. This study examines drought survival strategy and reproductive ecology of a small aquatic snake Seminatrix pygaea (Cope) in an isolated wetland. Seminatrix pygaea are atypical from most sympatric snake species in that (i) their small body size, reliance on aquatic prey, and high rates of evaporative water loss make them ill-suited to overland movement, and (ii) they may not be subject to costs typically associated with feeding during pregnancy. 4. We hypothesized that S. pygaea would survive periodic multiyear droughts by aestivating within the dried wetland, a survival strategy heretofore undocumented in snakes. Further, we hypothesized that if S. pygaea rely on 'typical' snake reproductive strategies of 'adaptive anorexia' and capital breeding, reproductive output would be reduced in the first wet year following drought. 5. By encircling a 10-ha wetland with a continuous drift fence before it refilled we were able to demonstrate that S. pygaea were present within the dried wetland prior to the onset of spring rains that refilled the wetland in 2003. Our results suggest that S. pygaea are capable of surviving multiyear droughts by aestivating within the dried wetland. 6. Despite having presumably depleted energy reserves during the drought, S. pygaea reproduced with the same frequency and fecundity during the first season following refilling of the wetland as in pre-drought years. 7. The ability of S. pygaea to rebound rapidly from the stresses of prolonged drought is due in part to their reproductive ecology. Seminatrix pygaea readily feed throughout pregnancy and consequently can rapidly translate high prey abundances into reproductive output through income breeding.     

Gripping during climbing of arboreal snakes may be safe but not economical

On the steep surfaces that are common in arboreal environments, many types of animals without claws or adhesive structures must use muscular force to generate sufficient normal force to prevent slipping and climb successfully. Unlike many limbed arboreal animals that have discrete gripping regions on the feet, the elongate bodies of snakes allow for considerable modulation of both the size and orientation of the gripping region. We quantified the gripping forces of snakes climbing a vertical cylinder to determine the extent to which their force production favoured economy or safety. Our sample included four boid species and one colubrid. Nearly all of the gripping forces that we observed for each snake exceeded our estimate of the minimum required, and snakes commonly produced more than three times the normal force required to support their body weight. This suggests that a large safety factor to avoid slipping and falling is more important than locomotor economy.     

Experimental study of alarm calls of the oriental tit (Parus minor) toward different predators and reactions they induce in nestlings

Anti-predatory strategies of birds are diverse and may include predator-specific alarm calls. For example, oriental tit (Parus minor) parents can distinguish snakes from other predators and produce snake-specific referential vocalizations ("jar" call) when a snake poses a threat to their nest. The “jar” call has a very specific function to induce fledging of nestlings close to fledging age. This reaction ensures nestlings' survival in natural encounters with snakes that are capable of entering nest cavities and kill entire broods. Sciurid rodents, like chipmunks, may pose a similar threat to cavity-nesting birds. We explored the hypothesis that parents use the fledging-inducing alarm vocalizations in this situation, because chipmunks, like snakes, can kill the brood upon entering the nest cavity. We compared alarm calls of parents toward two predators (chipmunk and snake) who pose a similar threat to the nestlings in a nest cavity, and toward an avian predator (Eurasian jay) who cannot enter nest cavities and poses no threat to the nestlings in a nest. Our results show that the vocal responses of oriental tits were different among the three predators. This suggests that the acoustic properties of vocal responses to predators are different between predators of a similar hunting strategy (nest-cavity entering). The playback of recorded vocal responses of parents to chipmunks did not trigger the fledging of old nestlings, whereas the vocalizations toward a snake did, as shown by earlier studies. Our study suggests that the vocal response of parents does not carry information about the ability of predators to enter the nest cavity and confirms the special status of alarm calls triggered by snakes.