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28 March 2016 The ecology of human-anaconda conflict: a study using internet videos
Everton B. P. Miranda, Raimundo P. Ribeiro, Christine Strüssmann
Author Affiliations +
Abstract

Human-wildlife conflict is a widespread problem that threatens both animals and local livelihoods. When this conflict involves predators, the additional risks to human life worsen the problem. The perceptions of human-predator conflict have been investigated multiple times, usually to generate data for conflict resolution. However, such efforts have largely involved mammals from the order Carnivora. In this work, we tested hypotheses about the feeding habits of two species of constricting anacondas from the genus Eunectes and human perception of risks and attitudes associated with such habits. In particular, we investigated the consequences for the snake after predation on domestic or wild animals. We also tested the relationship between human killing of anacondas and local development indicators – a proxy for general education level. Data were obtained from internet videos using a standardized method for information retrieval. A total of 330 videos of human-anaconda encounters were recovered from ten different South American countries. We found that visual evidence of a recent meal (distended abdomen) and predation on domestic animals did not affect the probability of the anaconda being killed, but this probability increased as the Human Development Index (HDI) diminished and as anaconda size increased. Although retaliatory killing is described as one of main causes of animal mortality following human-wildlife conflicts, our results suggest that killing of anacondas are not retaliatory or related to economic losses, but preventive, because these snakes are seen as life-threatening animals. Adding social context information on human-predator conflicts, together with taxon-free research on this subject can improve our knowledge about human-wildlife conflict. Further research could focus on the actual impacts (direct or indirect) of anacondas on stakeholders, and on the role of other non-mammalian predators in human-wildlife conflicts (whether actual or perceived).

Introduction

Human-wildlife conflict occurs when wildlife and people come into contact with negative impacts to one or both of them. It is a pervasive problem, especially when top predators threaten the food, safety, and economic resources of local stakeholders [1]. Unlike wild prey, domestic animals are highly vulnerable to predation due to low vigilance rates [234]. Moreover, they frequently occur in predictable high densities and are easier to catch than wild prey species [5,6]. Livestock consumption by predators and resulting retaliatory or preventive killing are a worldwide conservation concern [78910]. Persecution of predators on the one hand, and the need to conserve them on the other, create human-carnivore conflict [11].

The most widely studied of such conflicts have involved carnivore mammals, while similar research on other predators is scant, due largely to a series of biogeographical coincidences [12], as the developed nations – where most of the research on human-wildlife conflict is done [11] – are in the northern hemisphere. Because most top predators in northern ecosystems are mammals of the order Carnivora – with a peripheral role for raptors – most published research deals with conflict involving these species. Although this research focus does not reflect the realities of faunal composition in the tropics, it has nevertheless been followed by researchers in tropical regions.

Combine this with taxonomic xenophobia and the disproportionate attention received by charismatic species [13,14], and the result is a near-total lack of research on the role of non-mammalian predators in human-wildlife conflict. For instance, the CENAP (Brazilian government authority responsible for predation conflict) [15] deals solely with carnivorous mammals. However, in tropical regions top predator guilds have different compositions from those in the northern hemisphere, with eagles [16], crocodilians [17], giant snakes [18], and lizards [19] also occupying this role, demanding research on a much broader array of taxa than is currently the case [20].

Conservationists typically assume that people kill predators to reduce predation of domestic animals and/or life-threatening risks. Interviewing local people has been widely used to assess community perceptions of predators and to gather detailed information on human-predator interactions [2122232425]. Although ecological data are important in conservation decisions, two other aspects are also vital, and often neglected: the attitudes of local people toward wildlife, and the social context. Questionnaires and interviews are frequently used to measure perceptions and attitudes, but their application is limited in space and their wide-scale use would be prohibitively expensive. Socially contextualized information – such as the Human Development Index – can reveal the social variables of such conflicts [26,27], with the advantage that it can be retrieved from published sources.

Although regarded as a nontraditional scientific data source, the internet is creating a revolution in human communication, with effects ranging from massive information spreading on major conflicts [28] to broad availability of biologically useful data [29303132]. Internet sources can be standardized and used to gather information on human-predator conflicts with hundreds of professional and amateur internet videos containing information on foraging incidents, in detail and on a geographic scale that hardly could be attained by any other method. Analyses of these nontraditional data sources offer an empirical background to human-wildlife conflicts for which there are no published quantitative field data [33].

Boidae and Pythonidae snakes are known to prey on domestic animals [25,343536]. Boids, which occupy a variety of habitats and substrates in the Neotropics, are large sized, non-venomous, constricting species whose females are much larger than males [37]. In South America, the two most widely distributed and best-studied semiaquatic species are Eunectes notaeus (Cope 1887), the Yellow Anaconda, reaching nearly 3.7m and 29kg [38], and Eunectes murinus (Linnaeus 1758), the Green Anaconda, reaching 5.17m and 97.5kg [39]. Anacondas are killed in retaliation for livestock consumption and perceived risk to humans, and their fat is widely used for its supposed curative properties [40]. Anaconda leather has commercial value, but only in Argentina is there a sustainable management program for the Yellow Anaconda [41]. Snakes in the genus Eunectes are also wild-collected for the pet trade [42]. All anaconda species are included in CITES-Appendix II and have not yet been assessed under IUCN Red List categories and criteria.

We used internet videos to investigate attitudes of local people toward anacondas and to determine the extent, nature, and effects of human-anaconda conflict, based on the following hypotheses: (i) people are more inclined to retaliatory kill anacondas that preyed on pets or livestock; (ii) people are less inclined to kill anacondas that have eaten recently, assuming they pose less risk; (iii) people are more inclined to kill large-sized anacondas that are perceived to present greater risk; and (iv) anaconda killing is negatively correlated with Human Development Index (HDI). With these hypotheses we characterized the relationship between people and anacondas, and tested whether HDI affects human-wildlife conflict.

Methods

Data acquisition – Internet searches were made on Google Videos between August 2014 and May 2015. To find the videos we used the keywords boiuna, curiyú, mata-toros, sicuri, sucruiú, sucuri, sucuriju, sucurijuba, and yacumama, the vernacular English name anaconda, and the genus Eunectes. The common names used by Spanish, French, English and Portuguese speakers in South America allowed us to recover videos from different South American countries. For each keyword, we searched the first 100 results and collected data from the videos, together with site addresses. We did not include in our sample nature documentaries or videos produced in private captivity, zoological gardens, studios, or wildlife management facilities. We also checked our final database for duplicate videos (e.g., when a conflict event was depicted in a professional video and also in amateur videos). All site addresses are listed in the Appendix. Some of them contain scenes that may be disturbing for some viewers, as they involve animal cruelty.

Data standardization – For each video, we collected information on year, state-level location (Provincia, Departamento, Estado, etc.), and country. We noted the anaconda species, and recorded the prey species if the snake regurgitated or its stomach was cut open. Identification of most prey species was made directly from the videos, by the authors or by consulting taxon experts. If there was a bulge in the anaconda's stomach but prey could not be identified, it was labeled as “unknown.” Anaconda's body size was recorded in one out of five categories, chosen to minimize the error of estimation: less than 1 m; between 2 - 3 m; between 3 - 4 m, between 4 - 5 m, and more than 5 m. To check the error in our estimates, we asked two experienced biologists (Juan Draque and Mariano Barros, who had handled and measured hundreds of Yellow anacondas during an Argentinian sustainable management program) to produce two independent body size estimates of 30 randomly sampled videos. We then collated their estimates with ours as a test of our accuracy.

Since differently sized snakes could have differential chances of being videoed and posted on the internet (i.e., the “macho” effect increases the posting rate for larger snakes) we performed a two-sided Kolmogorov-Smirnov test between our estimated size distribution for both anaconda species and the size distribution of nearly seven hundred Green anacondas from Rivas [39]. We discovered that our distribution is close to reality, under the null hypothesis that the samples are drawn from different distributions (P = 0.38). Finally, we recorded whether or not the snake was intentionally killed in the video. Additionally, we obtained the Human Development Index (HDI) for each State or equivalent, in the same year of the video (or nearest, when there were no statistics for a specific year), using the reports of United Nations Development Program [4243444546]. We chose the HDI as a proxy for general education level at each location, since it is measured using the same methods all over the world. Besides education, HDI is a statistic composed of life expectancy and per capita income. For political reasons, Venezuela does not allow evaluations by the United Nations and so lacks data on HDI. Therefore, videos produced in that country were excluded from that analysis.

Statistical analyses –We used Fisher's exact test to investigate whether the proportion of anacondas killed when preying on livestock or pets differed from the proportion of anacondas killed when preying on wild prey [hypothesis (i)]. The same test was used to investigate whether the number of anacondas killed with obvious stomach contents (prey item identified or not) differed from the number of anacondas killed while lacking obvious stomach contents [hypothesis (ii)]. To test hypothesis (iii) we used a logistic regression, in which the dependent variable was binary (killed or not), and the independent variable was the body size estimate (categories 1 - 5). For hypothesis (iv) we also used a logistic regression, in which the dependent variable was binary (killed or not), and the independent variable was the HDI for the location of the video. We tested the accuracy of the anaconda's size estimate through a Spearman correlation between our own estimates and each independent series of estimates provided by the specialists. In order to model the stochastic correlation between the two estimates, we measured 10,000 Monte Carlo simulated Spearman correlations between our data and random samples of the specialists' data. All statistical analyses were made on R software using the Vegan package [48], and significance levels were established at 0.05.

Results

We sampled 330 videos filmed between 2002 and 2015, of which 274 were made by amateurs and 56 by professionals, generally from the news media. The majority of the videos were filmed in Brazil (269 videos), followed by Venezuela (14), Paraguay (seven), French Guyana (six), Colombia, Peru and Ecuador (three videos each), Argentina (two), and Trinidad & Tobago and Bolivia (one video each). We failed to establish the country for 19 videos. We were able to determine more precise location information (state level or equivalent) for 196 videos. Samples came from urban areas in 26.97% of the videos and from rural in 6.67%, while the degree of anthropization was not detectable in the remaining samples.

Body size estimates made by the specialist biologists were correlated with our own data, and there was also a correlation between the two independent specialists' estimations (Spearman correlation test, n = 30, ρ = 0.68, 0.63, and 0.57 for correlation between ours and each specialist's estimation, and between the two specialists, respectively). Monte Carlo randomization showed that this is not a product of chance (P < 0.01). We therefore consider that our size distribution estimation is close to reality.

The species depicted in the videos were Green anacondas in 297 samples and Yellow anacondas in 33 samples. No videos of the remaining members of the genus Eunectes – the Dark-spotted Anaconda Eunectes deschauenseei Dunn and Conant 1936, and the Bolivian Anaconda Eunectes beniensis Dirksen 2002 – were retrieved. In 78 videos, the snakes were killing, ingesting, digesting or regurgitating prey after being harassed, and only four of these were Yellow anacondas. In 27 of the videos that involved incidents of predation, prey was already inside the snake's digestive tract or highly digested and could not be identified. Among the prey items figured in the remaining 51 videos there were domestic animals in 23 of them (11 pets and 12 livestock), and wild animals in 28 (Table 1). Fifty-two videos showed people killing anacondas.

Table 1.

Descriptive data from Yellow and Green anacondas (Eunectes notaeus and Eunectes murinus) feeding habits as depicted in 78 internet videos. The percentage for each prey species is represented by % and the number of samples by n. Samples can be found by code on Appendix 1.

10.1177_194008291600900105-table1.tif

The rate of anacondas killed when preying on domestic animals was 21.7% compared to a 28.5% rate of anacondas killed when taking wild prey, but there was no statistical difference (two tailed Fisher's exact test, 50 d.f., P = 0.749). Snakes that had eaten recently (19.23%) were killed more frequently than those that had not (14.68%), but this difference has no statistical significance (two tailed Fisher's exact test, 329 d.f., P = 0.374). The Anaconda's size affected positively the probability of the snake being killed (logistic regression, 329 d.f., z-value = 3.11, P < 0.001). Anaconda killing following an encounter with humans is negatively and significantly related to changes in the Human Development Index of the location where the encounter occurred (logistic regression, 193 d.f., z-value = 2.91, P < 0.001; Figure 1).

Fig. 1.

A – Effect of body size (size classes' estimates, from one to more than five meters; see text for details) on the probability of an anaconda being killed, according to 330 internet videos; B – Effect of Human Development Index (HDI) on anacondas killing probability, in 196 locations for which we obtained information (state or equivalent).

10.1177_194008291600900105-fig1.tif

Discussion

Our study shows for the first time that in South America, anacondas can have high rates of predation on domestic animals, which comprised 41.82% of videoed anaconda prey. Capybaras (Hydrochoerus hydrochaeris) were the most common prey (17.8%), followed by domestic dogs (Canis lupus familiaris; 12.3%). Dogs as main prey have been noted in other studies of domestic animal predation by carnivores [49], as well as by crocodilians [50]. Several other domestic animals, such as cattle calves (Bos taurus), chickens (Gallus gallus), ducks (Cairina moschata), and cats (Felis catus) were also recorded being killed by anacondas. However, caution must be used in prey composition interpretation, because our method is likely to under-represent small prey and might also be biased toward domestic prey.

Although predation on domestic animals can lead to conflicts between their owners and predators [51], the rate of snakes killed after foraging on such food items in our sample of videos (15.7%) cannot be explained by food type, since it was lower than the rate at which anacondas were killed while eating wild animals. This phenomenon has been recorded elsewhere, when financial rewards have been given for not killing animals, even when there were confirmed instances of their having consumed livestock [52]. Although domestic animals are frequent items in the diet of anacondas, low retaliatory killing rates do not indicate persecution based solely on livestock consumption. Therefore, could rare predatory attacks on humans (a single occurrence in our sample, besides two defensive attacks) be the underlying cause of anaconda killing?

Current knowledge on human-predator conflict predicts that most killings are retaliatory or preventive [53]. Human-anaconda interactions in South America appear to be more complex, with causal factors normally unconsidered when dealing with mammalian predators. Although the videos did not provide a direct measure of body size of the anacondas, they demonstrated that large (> 5 m) snakes were more likely to be killed, and these are exclusively Green anacondas. While direct attacks on humans are rare, the increase in the killing of larger anacondas suggests that preventive or punitive killing is due to fear and could be one of the main reasons why people selectively kill the larger snakes (see an interesting discussion on the subject in 56).

Fear-based killing is corroborated by the strong influence of the HDI on killing probability. A non-feeding anaconda in a location with a HDI of 0.6 or less is six times more likely to be killed than one that is eating dogs in a location with a HDI of 0.7 or more. This suggests that, despite attacks on humans being rare events, the risk posed by anacondas still occurs in the collective imagination of less developed communities, resulting in the killing of these snakes at any given opportunity. Interestingly, this is contrary to current knowledge on the effects of HDI in conflict, since human-wildlife conflict is commonly associated with food security in less developed nations [54]. Furthermore, as reptiles, anacondas do not share with large cats or other carnivore mammals the same public concerns capable of preventing killing as a result of conflict [55]. Our results therefore add a social component to differences in predator killing probabilities, indicating a strong effect of human development on human-anaconda conflict.

Data for the current study were collected using a method that, although open to further improvements, allows low-cost access to information from a wide geographic range. Additionally, it allows obtaining data that were not biased by conservationist-observer presence. We emphasize that this is not the first time that non-traditional data spontaneously generated by its agents have been used to advance knowledge on conservation subjects [56]. The relationship between predators and people, especially considering the current widespread decline of predators, is a broad topic ready for online investigation.

Rather than definitively answering the questions related to human-anaconda conflict, our discoveries open a field of research rarely explored by tropical biologists. Here we have shown that the perceived risk a reptilian predator imposes on human lives can result in it being killed, even if the actual risk is slim. We encourage future researchers to try to quantify real and perceived losses inflicted on stakeholders by anaconda predation. We also suggest that this should be done for several other tropical predators that are frequently ignored by biologists working in the human-predator conflict field, such as crocodilians, eagles, and other large-sized predators that prey on domestic animals. Since anacondas are charismatic animals frequently depicted in popular books [57], infamous movies, music and mockumentaries, but rarely subjected to research, we expect our work to stimulate further investigation into other aspects of these iconic species.

Implications for conservation

Although lacking evaluation by IUCN, we believe that both anaconda species treated here (the Green and the Yellow anacondas) are not of conservation concern. Both species are flexible in habits, distributed over large areas that include several conservation units, and are capable of sustaining high harvest rates (see historical data from Argentina in 38). Their preventive killing in the context considered here probably has a negligible overall impact on range-wide populations. Our findings should be useful for conflict-related questions, since quantitative data on stakeholders' losses are unknown and conflict with non-mammalian predators is under-researched. Deliberate killing should also be investigated in the other two anaconda species – the Bolivian Anaconda and the Dark-spotted Anaconda – as these have much smaller ranges and are probably exposed to the same kind of persecution described in this study. Their occurrence in still remote areas (Beni river valley in Bolivia and Marajó region in northern Brazil, respectively; 48, 49) certainly accounts for the lack of videos depicting these two species. Since the largest animals are more likely to be killed – which in large constrictors are the females with highest reproductive output [38,39,60,61] – this could generate a conservation problem for these two smaller-ranged anaconda species.

Although many videos depicted anacondas either being killed or being harassed to a degree that led Brazilian authorities to prosecute their authors, several videos show the animals from an ecotourism perspective (see Appendix 1. samples 6, 126, 143, and 187 for instance). This points to a high tourism potential for these large snakes, already noted elsewhere [62]. Although restricted to a few areas of extremely clear water (e.g., 63 for Bonito and 64 for Nobres, both in Midwestern Brazil), ecotourism could be a way to positively incorporate the anacondas into local economies, as the management plan for skin trade is doing for the species in Argentina.

Acknowledgements

We thank the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) for grants to R. Ribeiro-Jr (PROPeq-UFMT 332/CAP/2013), E. Miranda (process #130873/2014-4), and C. Strüssmann (process #309541/2012–3), as well as for general financial support (“Edital Universal”; process #456497/2014-5). We also thank Fundação de Apoio à Pesquisa Científica e Tecnológica (FAPEMAT; process #155536/2014 and process #23038.007261/2014-32, grant 3530/2014, “Edital 008/2014–PRONEM/FAPEMAT/CAPES”). Jorge Menezes provided key inputs to the original discussions from which this research grew. Mariano Barros and Juan Draque kindly validated our size estimates and corrected the Spanish abstract. We acknowledge Adrian Barnett who reviewed the English, improving the quality of the article. We also thank numerous anonymous video makers who kindly responded to our requests for data. An anonymous reviewer kindly contributed to improving the final version of the paper.

References

1.

Inskip, C., Zimmermann, A., 2009. Human-felid conflict: a review of patterns and priorities worldwide. Oryx 43:18–34. Google Scholar

2.

Gustafsson, M., Jensen, P., de Jonge, F. H., Schuurman, T., 1999. Domestication effects on foraging strategies in pigs (Sus scrofa). Applied Animal Behavior Science 62:305–317. Google Scholar

3.

Abrahams, M., Sutterlin, A., 1999. The foraging and antipredator behaviour of growth-enhanced transgenic Atlantic salmon. Animal Behavior 58:933–942. Google Scholar

4.

Provenza, F., Villalba, J., Bels, V., 2006. Foraging in domestic herbivores: linking the internal and external milieux. In: Feeding in domestic vertebrates: from structure to behaviour. Bels, V., (Ed.), pp. 210–240. CABI Wuallingford, Oxfordshire. Google Scholar

5.

Sundararaj, V., McLaren, B., Morris, D., Goyal, S., 2012. Can rare positive interactions become common when large carnivores consume livestock? Ecology 93:272–280. Google Scholar

6.

De Azevedo, F. C. C., Murray, D. L., 2007. Spatial organization and food habits of jaguars (Panthera onca) in a floodplain forest. Biological Conservation 137: 391–402. Google Scholar

7.

Lyngdoh, S., Shrotriya, S., Goyal, S. P., Clements, H., Hayward, M.W., Habib, B., 2014. Prey preferences of the snow leopard (Panthera uncia): regional diet specificity holds global significance for conservation. PLoS One. 9: e88349. Google Scholar

8.

Palmeira, F., Crawshaw, P., 2008. Cattle depredation by puma (Puma concolor) and jaguar (Panthera onca) in central-western Brazil. Biological Conservation 141:118–125. Google Scholar

9.

Morehouse, A., Boyce, M., 2011. From venison to beef: seasonal changes in wolf diet composition in a livestock grazing landscape. Frontiers in Ecology and Environment 9:440–445. Google Scholar

10.

Estes, J. A., Terborgh, J., Brashares, J. S., Power, M. E., Berger, J., Bond, W.J., 2011. Trophic downgrading of planet Earth. Science 333:301–6. Google Scholar

11.

Treves, A., Karanth, K., 2003. Human-carnivore conflict and perspectives on carnivore management worldwide. Conservation Biology 17:1491–1499. Google Scholar

12.

Diamond, J., 1998. Guns, germs, and steel: A short history of everybody for the last 13,000 years. W. W. Norton & Company, New york. Google Scholar

13.

Bonnet, X., Shine, R., Lourdais, O., 2002. Taxonomic chauvinism. Trends in Ecology and Evolution 17: 1–3. Google Scholar

14.

Brooke, Z., Bielby, J., Nambiar, K., Carbone, C., 2014. Correlates of research effort in carnivores: body size, range size and diet matter. PLoS One. 9: e93195–e93195. Google Scholar

15.

IBAMA. 2015. CENAP.  http://www.icmbio.gov.br/cenap/carnivoros-brasileiros.html consulted at August 2015. Google Scholar

16.

Aguiar-Silva, F., Sanaiotti, T., Luz, B., 2014. Food habits of the Harpy Eagle, a top predator from the Amazonian rainforest canopy. Journal of Raptor Research 48:24–45. Google Scholar

17.

Nifong, J., Silliman, B., 2013. Impacts of a large-bodied, apex predator (Alligator mississippiensis Daudin 1801) on salt marsh food webs. Journal of Experimental Marine Biology and Ecology 440:185–191. Google Scholar

18.

Shine, R., Harlow, P., Keogh, J., 1998. The influence of sex and body size on food habits of a giant tropical snake, Python reticulatus. Functional Ecology 12:248–258 Google Scholar

19.

Doody, J.S., Soanes, R., Castellano, C.M., Rhind, D., Green, B., McHenry, C., 2015. Invasive toads shift predator-prey densities in animal communities by removing top predators. Ecology 96: 2544–2554. Google Scholar

20.

Glen, A., and Dickman, C., (Eds). 2014. Carnivores of Australia: Past, Present and Future. CSIRO Publishing, Sidney. Google Scholar

21.

Conforti, V., De Azevedo, F., 2003. Local perceptions of jaguars (Panthera onca) and pumas (Puma concolor) in the Iguacu National Park area, south Brazil. Biological Conservation 111: 215–221. Google Scholar

22.

Oli, M., Taylor, I., Rogers, M., 1994. Snow leopard Panthera uncia predation of livestock: an assessment of local perceptions in the Annapurna Conservation Area, Nepal. Biological Conservation 68: 63–68. Google Scholar

23.

Dar, N., Minhas, R., Zaman, Q., Linkie, M., 2009. Predicting the patterns, perceptions and causes of human–carnivore conflict in and around Machiara National Park, Pakistan. Biological Conservation 142: 2076–2082. Google Scholar

24.

Lucherini, M., Merino, M., 2008. Perceptions of human-carnivore conflicts in the High Andes of Argentina. Mountain Research and Development 28: 81–85. Google Scholar

25.

Goursi, U., Awan, M., Minhas, R., Ali, U., Kabir, M., Dar, N., 2012. Status and Conservation of Indian Rock Python (Python molurus molurus) in Deva Vatala National Park, Azad Jammu and Kashmir, Pakistan. Pakistan Journal of Zoology 44: 1507–1514. Google Scholar

26.

Kark, S., Tulloch, A., Gordon, A., Mazor, T., Bunnefeld, N., Levin, N., 2015. Cross-boundary collaboration: key to the conservation puzzle. Current Opinions in Environment and Sustainability 12:12–24. Google Scholar

27.

Nyirenda, V., Lindsey, P., Phiri, E., 2015. Trends in Illegal Killing of African Elephants (Loxodonta africana) in the Luangwa and Zambezi Ecosystems of Zambia. Environmental and Natural Resources Research 5:24–36. Google Scholar

28.

Comunello, F., Anzera, G., 2012. Will the revolution be tweeted? A conceptual framework for understanding the social media and the Arab Spring. Islam and Christian–Muslim Relations 23:453–470. Google Scholar

29.

Winterton, S.L., Guek, H.P., Brooks, S.J., 2012. A charismatic new species of green lacewing discovered in Malaysia (Neuroptera, Chrysopidae): the confluence of citizen scientist, online image database and cybertaxonomy. Zookeys 214:1–11. Google Scholar

30.

Bager, A., Borghi, C., Secco, H., 2015. The influence of economics, politics and environment on road ecology in South America. In: Handbook of Road Ecology. Van der Ree, R., Smith, D., and Grilo, C., (Eds). Wiley-Blackwell, Chichester. Google Scholar

31.

Sullivan, B.L., Wood, C.L., Iliff, M.J., Bonney, R.E., Fink, D., Kelling, S., 2009. eBird: A citizen-based bird observation network in the biological sciences. Biological Conservation 142:2282–2292. Google Scholar

32.

Kawrykow, A., Roumanis, G., Kam, A., Kwak, D., Leung, C., Wu, C., 2012. Phylo: a citizen science approach for improving multiple sequence alignment. PLoS One 7: e31362. Google Scholar

33.

Bizri, H., Morcatty, T., Lima, J., Valsecchi, J., 2015. The thrill of the chase: uncovering illegal sport hunting in Brazil through YouTubeTM posts. Ecology and Society 20:1–30. Google Scholar

34.

Strüssmann, C., 1997. Hábitos alimentares da sucuri-amarela, Eunectes notaeus Cope, 1862, no Pantanal matogrossense. Biociencias 5:35–52. Google Scholar

35.

Bhupathy, S., Ramesh, C., Bahuguna, A., 2014. Feeding habits of Indian rock pythons in Keoladeo National Park, Bharatpur, India. Herpetological Journal. 24:59–64. Google Scholar

36.

Shine, R., Harlow, P.S., Keogh, J.S., 1998. The influence of sex and body size on food habits of a giant tropical snake, Python reticulatus. Functional Ecology 12: 248–258. Google Scholar

37.

Henderson, R., and Powell, R., Eds. 2007. The biology of boas and pythons. Eagle Mountain Publishing, Utah. Google Scholar

38.

Waller, T., Micucci, P., Alvarenga, E., 2007. Conservation biology of the yellow anaconda (Eunectes notaeus) in northeastern Argentina. In: Biology of the boas and pythons. Henderson, R.W., and Powell, R., (Eds). Eagle Mountain Publishing, Utah. Google Scholar

39.

Rivas, J., 2015. The life history of the green anaconda (Eunectes murinus) with emphasis on its reproductive biology. CreateSpace, South Carolina. Google Scholar

40.

Alves, R.R.N., Filho, G.A.P., De Lima, Y.C.l.C., 2006Snakes used in ethnomedicine in northeast Brazil. Environmental Development and Sustainability 9: 455–464. Google Scholar

41.

Micucci, P., Waller, T., 2007. The management of Yellow Anacondas (Eunectes notaeus) in Argentina: From historical misuse to resource appreciation. Iguana 14:160–171. Google Scholar

42.

Romagosa, C., 2014. Patterns of Live Vertebrate Importation into the United States: Analysis of an Invasion Pathway. In: Invasive Species in a Globalized World: Ecological, Social, and Legal Perspectives on Policy. Keller, R. P., Cadotte, M. W., and Glenn, S., (Eds). University of Chicago Press, Chicago. Google Scholar

43.

PNUD. 2010. Atlas do Desenvolvimento Humano no Brasil.  http://www.atlasbrasil.org.br/2013/pt/consulta/ consulted at 24 May 2015 Google Scholar

44.

PNUD. 2011. Colombia Rural: Razones para la esperaza. Informe Nacional de Desarollo Humano.  www.pnud.org.co/sitio.shtml?apc=aBa020081–&x=65970&s=j#.VWINp09Viko consulted at 24 May 2015 Google Scholar

45.

PNUD. 2003Informe Nacional Sobre Desarrollo Humano Paraguay.  http://desarrollo.edu.py/uploads/2013/01/informe-desarrollo-humano-2003.pdf consulted at 3 Aug 2015 Google Scholar

46.

PNUD. 2013. Cambio climático y territorio: Desafíos y respuestas para un futuro sostenible Informe sobre Desarrollo Humano.  www.pe.undp.org/content/peru/es/home/library/poverty/Informesobredesarrollohumano2013/IDHPeru2013.html consulted at 26 May 2015 Google Scholar

47.

PNUD. 2011. Argentina en un mundo incierto: Asegurar al desarrollo humano en el siglo XXI.  www.ar.undp.org/content/argentina/es/home/library/human_development.html consulted at 24 May 2015 Google Scholar

48.

Oksanen, J., Kindt, R., Legendre, P., O'Hara, B., Stevens, M.H.H, Oksanen, M.J., 2007The vegan package. Community Ecology Package. Google Scholar

49.

Athreya, V., Odden, M., Linnell, J., 2014. A cat among the dogs: leopard Panthera pardus diet in a human-dominated landscape in western Maharashtra, India. Oryx 1–7. Google Scholar

50.

Mawson, P., 2004. Crocodile management in Western Australia. Proceedings of the 17th Working Meeting of the IUCN-SSC Crocodile Specialist Group 28–37. Google Scholar

51.

Hariohay, K., Røskaft, E., 2015. Wildlife Induced Damage to Crops and Livestock Loss and how they Affect Human Attitudes in the Kwakuchinja Wildlife Corridor in Northern Tanzania. Environmental and Natural Resources Research 5:72–79. Google Scholar

52.

Liu, F., McShea, W.J., Garshelis, D.L., Zhu, X., Wang, D., Shao, L., 2011Human-wildlife conflicts influence attitudes but not necessarily behaviors: Factors driving the poaching of bears in China. Biological Conservation 144:538–547. Google Scholar

53.

Moleón, M., Sánchez-Zapata, J.A., Gil-Sánchez, J.M., Barea-Azcón, J.M., Ballesteros-Duperón, E., Virgós, E., 2011Laying the foundations for a human-predator conflict solution: assessing the impact of Bonelli's eagle on rabbits and partridges. PLoS One 6: e22851. Google Scholar

54.

Peterson, M.N., Birckhead, J.L., Leong, K., Peterson, M.J., Peterson, T.R., 2010. Rearticulating the myth of human-wildlife conflict. Conservation Letters 3:74–82. Google Scholar

55.

Marchini, S., Macdonald, D., 2012. Predicting ranchers' intention to kill jaguars: case studies in Amazonia and Pantanal. Biological Conservation 147: 213–221. Google Scholar

56.

McClenachan, L., 2009. Documenting loss of large trophy fish from the Florida Keys with historical photographs. Conservation Biology 23:636–43. Google Scholar

57.

Murphy, J.C., Henderson, R.W., 1997. Tales of giant snakes: a historical natural history of anacondas and pythons. Krieger Pub. Co., Malabar. Google Scholar

58.

Plotkin, R., Riding, S., 2011. Biogeography of the Llanos de Moxos: natural and anthropogenic determinants. Geographica Helvetica 3: 183–192. Google Scholar

59.

Waller, T., Micucci, P., 1993. Estado actual del conocimiento de la biología, comercio y conservación de las boas neotropicales: Géneros Boa L. (1758) y Eunectes Wagler (1830)(Reptilia: Serpentes: Boidae). Informe inédito preparado por TRAFFIC Sudamérica. Google Scholar

60.

Shine, R, Harlow, PS, Keogh, JS., 1998. The allometry of life-history traits: insights from a study of giant snakes (Python reticulatus). Journal of Zoology 244: 405–414. Google Scholar

61.

Cardozo, G., Chiaraviglio, M., 2011. Phenotypic plasticity of life history traits in relation to reproductive strategies in Boa constrictor occidentalis. Evolution and Ecology 25:1163–1177. Google Scholar

62.

Barrio-Amorós, C., Manrique, R., 2007. Historia natural de la anaconda (Eunectes murinus, Linnaeus, 1758) en Los Llanos de Venezuela. Una perpectiva ecoturistica. Fundación AndígenA, Mérida. Google Scholar

63.

Arruda, D. O., Oliveira, G.M., Mariani, M.A.P., 2014. Competitiveness of tourism productive system in Bonito, MS, Brazil, from a resource-based view. Interações 15: 399–408. Google Scholar

64.

Lemes, M.T., Nunes, J.R., Nunes, P.A., Oliveira, S.S., 2014. Contribution of Ecotourism and Environmental Education at a resort located in the city of Nobres (MT, Brazil). Revista Brasileira de Ecoturismo 7: 151–167. Google Scholar

Appendices

Appendix 1:

ID: individual sample number. Link: site address for each sample. Category: amateur (unprofessional recording) and professional (recorded by TV news teams). Year: year when video was recorded. HDI: Human Development Index in state (or equivalent) level as shown in 43–47. ISO Code: country code following ISO 3166-1 alpha-3. Species: scientific name of anaconda species in the video. Size (1-5): size estimates from one to more than five meters (see text for details). Predation (0 or 1): if the videoed anaconda was involved in a predation incident. Prey species: scientific name of prey species involved (NI stands for Not Identified). Prey category: wild when native prey was killed and domestic when pet or livestock were killed. Habitat category: separated in urban and rural. Kill: 1 if anaconda was killed in the video and 0 if it was not.

10.1177_194008291600900105-table2.tif
© 2016 Everton B. P. Miranda, Raimundo P. Ribeiro-Jr., and Christine Strüssmann. This is an open access paper. We use the Creative Commons Attribution 4.0 license http://creativecommons.org/licenses/by/4.0/. The license permits any user to download, print out, extract, archive, and distribute the article, so long as appropriate credit is given to the authors and source of the work. The license ensures that the published article will be as widely available as possible and that your article can be included in any scientific archive. Open Access authors retain the copyrights of their papers. Open access is a property of individual works, not necessarily journals or publishers.
Everton B. P. Miranda, Raimundo P. Ribeiro, and Christine Strüssmann "The ecology of human-anaconda conflict: a study using internet videos," Tropical Conservation Science 9(1), 43-77, (28 March 2016). https://doi.org/10.1177/194008291600900105
Received: 23 September 2015; Accepted: 27 November 2015; Published: 28 March 2016
KEYWORDS
Boidae
Eunectes murinus
Eunectes notaeus
human-wildlife conflict
livestock predation
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