Does the rattle of Crotalus durissus terrificus reveal its dietary history?
© Martinez et al.; licensee BioMed Central Ltd. 2014
Received: 30 August 2014
Accepted: 4 December 2014
Published: 9 December 2014
Environmental devastation threatens the survival of many species, including venomous snakes such as the South American rattlesnake Crotalus durissus terrificus. This observation is based on the decrease of snakes collected and donated to Brazilian research institutes. Nevertheless, some individuals have managed to survive and procreate. The question is how these snakes are adapting in these new environmental conditions.
To answer it, the carbon-13 level of rattlesnakes and their feed (either laboratory or wild mice) was evaluated by isotope-ratio mass spectrometry. Thus, rattle segments from 16 adults and 15 offspring of captive snakes, and of three wild newborn C. d. terrificus were evaluated as well as 17 Mus musculus mice captured in traps, four live feeder mice and the ration offered to mice at animal houses.
The isotopic exchange time of the captive adult snakes (n = 16) varied between 33 and 37 months and of captive-born animals (n = 15), until reaching a plateau of equilibrium, varied from 18 to 24 months. Regarding the captured Mus musculus (n = 17), 88.23% (n = 15) were from a C4 environment. Of the six rattle rings from offspring of captured C. d. terrificus, five were from a C4 environment, whereas of the 170 rattle rings studied, 60% originated from a C3 environment and 40% from a C4. The same carbon-13 values were found in captive snakes.
Based on the present results, it can be inferred that most C. d. terrificus snakes (60%) fed animals from a C3 environment; birds consist of an alimentary alternative for snakes, as well as rodents, small reptiles and amphibians; different venom compositions among snakes from the same region may be related to the food type; the primary rattle of offspring reflects the maternal diet during gestation; and, finally, the different rattle rings indicate the alimentary history of these animals.
The South American rattlesnake Crotalus durissus terrificus, characterized by a caudal rattle, has proven to be able to procreate and survive in hostile environments. Once born, the offspring carry at the caudal tip a single ring denominated the primary rattle. At each molting, which generally occurs every 6 to 12 months depending on the diet, a new ring is formed. Throughout the life of these animals, they accumulate numerous rings, thus augmenting their rattle permanently. Environmental devastation requires these animals to adapt to new living conditions. Although the number of human accidents has increased in certain regions of Brazil, the number of specimens captured and donated to research institutes has diminished [1–4]. The question is how are these snakes adapting to and surviving in new environmental conditions?
To answer this query, the authors analyzed the isotope carbon-13 (δ 13C) of rattle segments from young and adult C. d. terrificus rattlesnakes as well as of food offered to them by means of mass spectrometry [5, 6]. This research was based on the knowledge that plants around the globe present different biochemical pathways, by absorbing molecules in their stable isotopes, especially carbon (12C, 13C), hydrogen (1H, 2H), oxygen (16O, 17O, 18O), nitrogen (14 N, 15 N) and sulfur (32S, 33S, 34S, 36S). During photosynthesis, when carbon fixation results in three-carbon atoms, the process is called C3 photosynthetic plant cycle. When the initially formed sugars have four carbon atoms, the process is called C4 photosynthetic plant cycle. Group C3 comprise approximately 86% of plant species, including hardwoods, pine and eucalyptus forests, rice, soy, other leguminous and fruit-bearing trees. C4 plants comprise grasses, corn and sugarcane (see Additional file 1) .
According to Vogel , the isotopic ratios and δ13C‰ values in C3 and C4 plants are expressed in the Pee Dee Belemnite (PDB) standard. The standard was named after a Cretaceous marine fossil, Belemnitella americana, found in the Pee Dee Formation in South Carolina, USA. This material had an anomalously high 13C:12C ratio (0.0112372), and was established as δ13C value of zero. The δ13C‰ of C3 plants varies from −22‰ to −33‰ with an average value of −26.7‰ whereas that of C4 plants ranges from −9‰ to −16‰, determining an average value of −12.6‰ and sample mean of −12.5‰. According to Martinez , environments that present intermediate values between −16‰ and −22‰ can be classified as partially C3 or C4. Thus, values between −16‰ and −17.2‰ indicate partially C4 plants and between −22‰ and −23.23‰ would suggest partially C3 plants. Thus, the isotopic variations of δ13C‰ found in organic matter may be used in the quality control, authentication and traceability of products originating from C3 and C4 plant environments .
The objective of this work was to evaluate the levels of (δ13C) in the rattle rings of C. d. terrificus snakes captured and born in captivity, in captured and laboratory mice, and in the ration offered to mice for diagnosing whether the alimentary history of the snakes is related to the C3 or C4 environment or both.
Captive animals were donated by the Center for the Study of Venoms and Venomous Animals (CEVAP) of São Paulo State University (UNESP) based in Botucatu, SP, Brazil (latitude 22° 53′ 09“ South, longitude 48° 26′ 42” West, and average altitude 804 meters) and by the Butantan Institute (IB) in São Paulo, Brazil (latitude 23° 32′ 51“ South, longitude 46° 38′ 10” West and altitude 760 meters).
We evaluated segments of rattles of 16 adult C. d. terrificus snakes kept in captivity (11 at CEVAP and five at IB) and 15 newborn snakes (four born in CEVAP and 11 in IB). Four mice (two from the CEVAP animal house and two from IB) and samples of feed offered to rodents reared in IB and CEVAP were studied.
A field study was conducted in the city of Pardinho, about 20 km from Botucatu (latitude 23° 4′ 52“ South, longitude 48° 22′ 25” West and average altitude 898 meters) where most of the snakes donated to CEVAP were captured. At this site, pitfall traps were placed to capture mice, small rodents and newborn snakes [9, 10]. Three newborn C. d. terrificus and 17 Mus musculus mice captured in these traps in Pardinho were studied.
Collection of material
The rattle of each C. d. terrificus snake was manually removed, then counted and placed into a tube of transparent plastic. The rattles were separated and identified one-by-one according to the origin of the animal. In total, 34 rattles were collected and 170 rings analyzed.
Captured mice and those provided by IB and CEVAP were killed according to the guidelines of the Ethics Committee on Animal Experimentation. Authorization for the field study was obtained from the Brazilian Institute of Environment and Renewable Natural Resources (IBAMA) – authorization for scientific purpose (number 13999–1).
For measurement of the isotopic ratio of carbon-13 (δ13C) in snake rattles, mice and their ration, three samples weighing from 50 to 70 μg were inserted into capsules maintained in a refrigerator at +4°C, in the laboratory of the Stable Isotopes Center of UNESP, Botucatu, SP. The employed methodology was proposed by Tieszen et al. , with adaptations by Ducatti et al.. The isotopic ratios of 13C/12C were measured in a Delta V Advantage Isotope Ratio Mass Spectrometer (Thermo Fisher Scientific, USA). Isotopic ratio values were expressed as delta per thousand (δ) relative to the PDB international standards for 13C.
The analysis and δ13C curve values obtained for each animal were obtained statistically by the Minitab method of regression for non-linear equations .
Ethics committee approval
This study was approved on April 29, 2008 by the Brazilian Institute of Environment and Renewable Natural Resources (IBAMA) – SISBIO (authorization for activities with scientific purposes) under protocol number 13999–1.
By analyzing the samples and diet of rodents provided by CEVAP and IB, the following results were obtained: the average isotopic values of δ13C of rodents from CEVAP and IB animal house were respectively −21.46‰ ± 0.15‰ and −22.03‰ ± 0.07‰; for the ration given to rodents, the respective mean values for CEVAP and IB were −21.56‰ ± 0.08‰ and −22.56‰ ± 0.02‰.
Figure 1 shows the analysis of the δ13C results obtained from the nine segments of rattlesnake 1, from Botucatu, captured in a maize crop and kept for at least 24 months in CEVAP. The analysis revealed isotopic δ13C values of −13.98‰ for the first segment, −18.56‰ for the fifth and −13.28‰ for the sixth segment. The results observed in the seventh, eighth and ninth segments were respectively −17.34‰, −17.96‰ and −17.51‰. Figure 1 shows these results.
Figure 2 shows the analysis of the δ13C results obtained from the eight segments of rattlesnake 4, which was kept in captivity at CEVAP. Its respective δ13C isotopic values were −20.77‰ for the first segment, −14.5‰ for the second and −13.46 ‰ for the third segment. This snake was held in captivity for at least 42 months, where it received a diet of mice bred in CEVAP. The results observed in the fourth, fifth, sixth, seventh and eighth segments were respectively −17.26‰, –18.28‰, −19.44‰, −19.9‰ and −20.53‰, as shown in Figure 2.
The δ13C results obtained from the six segments of the mother rattlesnake 1 were as follows: the first segment showed a δ13C isotopic value of −17.45‰, whereas the second, third, fourth, fifth and sixth produced respective percentages of −14.67‰, −16.38 ‰, −14.98 ‰, −16.09‰ and −16.62‰. When this snake was captured and taken to IB, it had six segments in its rattle. One month later it gave birth to three snakelets whose δ13C values measured in the first segments were respectively –17.55‰., −17.09‰ and −17.90‰. The mother rattlesnake 2, held captive for a month at IB, had the respective δ13C values for its segments: −12.65‰, −14.97‰, −13.26‰ and −12.21‰. The five snakes born in captivity showed δ13C values for the primary/first segment of −12.59‰, −12.51‰, –12.94‰, −13.65‰ and −12.72‰. Figure 4 displays the results.
The mice bred in CEVAP and IB animal houses showed respective δ13C averages of −21.46 ± 0.15‰ and −22.03 ± 0.07‰. The two mice caught in the partially C3 environment showed average δ13C values of −18.73 ± 0.07‰, whereas the fifteen mice captured in the C4 environment presented a δ13C average of −11.92 ± 0.05‰. For the primary and second segments, the second wild newborn (F2) presented respective δ13C values of −19.57‰ and −16.57‰ versus −12.57‰ and –11.50‰ for the first wild newborn (F1) and −13.89‰ and −11.59‰ for the third wild newborn (F3).
The isotopic profile (Figure 1) shows that, from birth to the development of the fourth segment (around 18 months of age), the first snake had consumed a diet based on animals living in an environment closely resembling C4. The fifth segment showed an isotopic value compatible with partially C3; in other words, there was a dietary change in prey that had fed on fruits, rice, soy, coffee and large trees. In the sixth segment the snake returned to eating animals from a strictly C4 environment, at which point it was captured and donated to CEVAP, initiating a controlled diet based on rodents from the animal house that consume solely balanced feed produced from a partially C3 environment. There was a change in the nature of the food energy source from the old environment (C4) to the captive (C3). These results are compatible with its life history, since this snake was captured in a maize crop – the representative plant of C4 environment.
Isotopic analysis of the profile of the rattlesnake 4 (Figure 2) shows that it was born in a mixed C3-C4 environment, where it remained for approximately six months and was then captured and taken to CEVAP. In captivity, it was offered live rodents that had the same isotopic profile of the ration they received. To complete the turnover of carbon, this animal had to be held in captivity with the same dietary energy supply for at least 33 months. Therefore, there is a slower turnover due to slow metabolism that provokes a slow rate of tissue production, which includes the rattle. These data agree with those by Mizutani et al. , which suggest that animals with a slow metabolism present a slow turnover, while those with an accelerated metabolism show a fast turnover.
Figure 3 shows the profile of the offspring from a mother recently captured and donated to CEVAP, indicating that both snakelets have the same isotopic initial values, namely −16.2‰. Both received since birth a diet of rodents from the animal house. Since it were animals in the growth phase, we found that the turnover was faster than that of adult animals acquiring, therefore, the isotopic equilibrium earlier. In this case, the first animal reached the equilibrium level at approximately 18 months and the second at around 28 months. The observation of these animals in the growth phase corroborated the study by Mizutani et al. , which showed that accelerated metabolism causes a rapid turnover. The isotopic values of both primary segments proves that they are from the same litter.
Figure 4 displays an analysis of the mothers and their offspring. The first mother was from a partially C4 environment while the second mother originated from a strictly C4 environment. The offspring of the first mother showed isotopic values from the same environment. These snakes were pregnant in nature when captured and donated to the IB. After a period of approximately one month, the first gave birth to three snakes and the second, five. All were born with the primary segment. Isotopic analysis of δ13C in mother rattlesnake 1 and its three offspring revealed that the last segment of the mother rattle was similar to those of the snakelets. Similar results were observed for mother rattlesnake 2 and its offspring. These findings show that the mother’s diet in nature can be traced in offspring rattles. There was also a small fractionation factor between mother and newborn snakes of around ± 1‰ for δ13C, which may suggest that the isotopic values of the primary segment of the offspring are close to those of the last segment of the mother.
Figure 5 shows that the majority of mice (88.23%) captured in the field were from a C4 environment. Regarding the second wild newborn snake, it was originally from a partially C3 environment and after migrated to a partially C4. The others were born in a C4 environment and remained in the same.
Figures 6 and 7 display a histogram and the mean values of δ13C in the 170 rattle segments of the studied snakes, according to the distribution of environments. It was verified that most of the values (58%) belong to an environment that is partially C3.
Additional file 1 shows two biochemical pathways of carbohydrate synthesis that carbon isotopes can follow in nature. The animals that feed on C3 and C4 plants will incorporate both types of isotopes. Thus, it may be concluded that Crotalus durissus terrificus snakes are predators of animals such as birds, mammals, reptiles and amphibians that had fed on C3 and C4 plants. The rattle rings enabled not only a retrospective analysis of the lifelong alimentary history but also speculation as to whether they were also eating birds, as can be observed in Figure 8, which provides a gain in the competition for survival in environments that are increasingly hostile and devastated. In relation to mice, it must be emphasized that those captured in a natural setting were predominantly consuming C4 plants. In captivity, these animals are fed ration produced from C3 plants, especially rice, soy and other legumes. Consequently, upon entering captivity, all the snakes alter their isotopic profile to that of a C3 environment.
Between 1993 and 1995 Sant’Anna and Abe  analyzed the stomach contents of 633 rattlesnakes (C. d. terrificus) in southeastern Brazil. The authors observed that the gastric and intestinal content was constituted mostly of the remains of rodents and small marsupials, and noted that newborn rattlesnakes fed primarily on rodents and presented the lowest rate of animals with stomach content . It should be highlighted that on that occasion, no birds were found in the gastric content. The current observations show that these animals incorporated birds in their diet, as shown by Figure 8 recently taken in CEVAP captivity.
Based on the results, we conclude that:
● Crotalus durissus terrificus eat animals whose diets comprise both C3 and C4 plants.
● The rate of complete turnover of newborn snakes born in captivity until reaching the equilibrium level varies between 18 and 24 months.
● The rate of complete turnover of adults held in captivity until reaching the equilibrium level varies from 33 to 36 months.
● The primary rattle of newborn snakes reflects the mother’s diet during pregnancy, which can be confirmed by isotopic analysis of the last rattle segment the mother’s body.
● The ration produced in Brazil and offered as food to the rodents in captivity is produced essentially from rice, soy and other plants.
● It is possible to speculate that besides rodents, snakes may also be feeding on birds.
● One may also question whether this new behavior could alter the future composition of the venom of these snakes.
● Further studies are required to confirm all or some of these hypotheses.
The authors would like to thank the State of São Paulo Research Foundation (FAPESP, proc. n. 2007/05159-7 and 2008/57411-4) and the National Council for Scientific and Technological Development (CNPq, proc. n. 473622/2009-2).
- Barraviera B, Bonjorno JC Jr, Arakaki D, Domingues MA, Pereira PC, Mendes RP, Machado JM, Meira DA: A retrospective study of 40 victims of Crotalus snake bites. Analysis of the hepatic necrosis observed in one patient. Rev Soc Bras Med Trop 1989, 22(1):5–12. 10.1590/S0037-86821989000100002View ArticlePubMedGoogle Scholar
- Azevedo-Marques MM, Cupo P, Hering SE: Acidentes por animais peçonhentos. Medicina, Ribeirão Preto 1992, 25: 539–554.Google Scholar
- Sgarbi LPS, Ilias M, Machado T, Alvarez L, Barraviera B: Human envenomations due to snakebites in Marília, state of São Paulo, Brazil. A retrospective epidemiological study. J Venom Anim Toxins 1995, 1(2):70–78.View ArticleGoogle Scholar
- Duarte MR, Menezes FAM: Is the population of Crotalus durissus (Serpentes, Viperidae) expanding in Brazil? J Venom Anim Toxins incl Trop Dis 2013, 19: 30. doi:10.1186/1678–9199–19–30 10.1186/1678-9199-19-30PubMed CentralView ArticlePubMedGoogle Scholar
- Mizutani H, Kubaya Y, Wada E: Nitrogen and carbon isotope compositions relate linearly in cormorants tissues and its diets. Isot Environ Health Stud 1991, 27(4):166–168. 10.1080/10256019108622500View ArticleGoogle Scholar
- Ducatti C, Carrijo AS, Pezzato AC, Mancera PFA: Modelo teórico e experimental da reciclagem do Carbono–13 em tecidos de mamíferos e aves. Sci Agric (Piracicaba, Braz) 2002, 59(1):29–33. 10.1590/S0103-90162002000100003View ArticleGoogle Scholar
- Vogel JC: Variability of Carbon Isotope Fractionation During Photosynthesis. In Stable Isotopes and Plants Carbon-Water Relations. Edited by: Saugier B, Ehleringer JR, Hall AE, Farguhar GD. San Diego: Academic Press; 1993:29–46.View ArticleGoogle Scholar
- Martinez MG: Feeding history of Crotalus durissus terrificus snakes by analysis of Carbon-13 (δ13C) isotope from the rattle. J Venom Anim Toxins incl Trop Dis 2010, 16(1):186–187. 10.1590/S1678-91992010000100019View ArticleGoogle Scholar
- Heyer WR, Donnelly RA, McDiarmid RW, Hayek LC, Foster MS: Measuring and Monitoring Biological Diversity: Standard Methods for Amphibians. Washington: Smithsonian Institution Press; 1994.Google Scholar
- Cechin SZ, Martins M: Eficiência de armadilhas de queda (pitfall traps) em amostragens de anfíbios e répteis no Brasil. Rev Bras Zool 2000, 17(3):729–740. 10.1590/S0101-81752000000300017View ArticleGoogle Scholar
- Tieszen LL, Boutton TW, Tesdahl KG, Slade NA: Fractionation and turnover of stable carbon isotopes in animal tissues: implications for δ13C analysis of diet. Oecologia (Berlin) 1983, 57: 32–37. 10.1007/BF00379558View ArticleGoogle Scholar
- Microcal Software Origin® 6.0. Professional: Origin Data Analysis and Technical Graphics. Northampton, USA: Microcal Software Inc; 1999.Google Scholar
- Sant’Anna SS, Abe AS: Diet of the rattlesnake Crotalus durissus in southeastern Brazil (Serpentes, Viperidae). Stud Neotrop Fauna E 2007, 42(3):169–174. 10.1080/01650520601148313View ArticleGoogle Scholar
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