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CARLOS
JESUS
BALDERAS
VALDIVIA (e-mail: cjbv@servidor.unam.mx), Laboratorio de
Biodiversidad, Direcci6n General de Divulgaci6n de
la
Ciencia,
Universmn,
UNAM,
Zona
Cultural Universitaria,
CP
04510,
Mexico, D.F.
CROTALUS
RA
VUS (Mexican Pygmy Rattlesnake).
DIET.
There
are few reports regarding the feeding habits
of
Crotalus ravus.
However, lizards (Sceloporus grammicus, S. megalepidurus),
mammals (Mus musculus, Microtus mexicanus), and insects (He-
miptera and Orthoptera) have been reported in the diet
of
this spe-
cies (Uribe-Pena et al. 1999. Anfibios y Reptiles de las Serranfas
del Distrito Federal, Mexico. Instituto de Biologfa, Universidad
Nacional Aut6noma de Mexico. 119 pp.; Mendoza-Hernandez et
al. 2004. Herpetol. Rev. 35:63).
In May 2001 we found a C. ravus at the base
of
a cactus ( Opuntia
sp.) near
La
Preciosa Lake (19 .3678°N, 97 .3867°W, WGS84; 2040
m), Las Minas,Puebla State,Mexico. The snake was eating an adult
Sceloporus spinosus. Photographic vouchers (MZFC 1604--05) are
in the Herpetological Collection
of
Museo de Zoologia, Facultad
de Ciencias, Universidad Nacional Aut6noma de Mexico.
Furthermore, on 12 May 2007 we collected an adult female
C. ravus (167
mm
SVL, 186
mm
TL), in Delegaci6n Magdalena
Contreras (19 .2879°N, 99 .2670°W, WGS84; 2580 m) in the south-
ern mountains
of
Distrito Federal, Mexico. The specimen (MZFC
20902) was found crossing a trail in oak forest. A fragment
of
a
snake tail was found in the snake's stomach.
We
identified the prey
as
Thamnophis scalaris, by comparing the tail fragment to the tails
of
other snakes collected in the same area. This is the first report
of
a snake in the diet
of
C. ravus.
We
thank Manejo de Ecosistemas y Desarrollo Humano, Uni-
versidad Nacional Aut6noma de Mexico (SDEI-PTID-02) for
financial support.
Submitted by ISRAELSOLANO-ZAVALETA(e-mail: crota-
lus.viper@gmail.com),
URI
OMAR
GARCIA-VAZQUEZ
and
MARTHA
L.
CALDERON-ESPINOSA,
Museo de Zoologfa,
Facultad de Ciencias, Universidad Nacional Aut6noma de Mexico,
Apartado Postal 70-399, Mexico, Distrito Federal 04510, Mexi-
co.
EUNECTES
MURINUS
(Green Anaconda).
LONGEVITY.
Anacondas and other large reptiles tend to live many years and
grow slowly later in life. However, long-term data on growth
rates for wild snakes are in short supply. Here we report recapture
of
a Eunectes murinus after
13
years. These observations were
made in the course
of
conducting an on-going mark-recapture
project (running since 1992) in the Venezuelan llanos, Distrito
M uiioz' A pure
state
(7
.5°N' 69
.3
°W). All snakes were marked
using scale clipping and by copying the ventral pattern covering
the first
15
subcaudal scales (Rivas
et
al. 2007. In Henderson and
Powell [eds.], Biology
of
the Boas and Pythons, pp. 128-138.
Eagle Mountain Publishing Company, Eagle Mountain, Utah).
On 27 August 1994 we captured a female (E548, 324 cm
SVL,
21
kg). Thirteen years later on
19
March 2007, we caught
E548 again and although the scale clipping mark was difficult
to
read,
we
were able to identify the individual unequivocally
by comparing the subcaudal pattern with our records. Upon
recapture E548 measured 366
cm
SVL and 25 kg. E548 was
wounded, weakened, and had a subcutaneous nematode (possibly
Dracunculus sp.) which has been found in other individuals in
this population (Calle et al. 1994.
J.
Zoo. Wild. Med. 25:53-64).
This may be the longest recapture record
of
any individual
snake in the wild. Twelve-year recaptures have been reported
by Madsen and Shine (2000. J. Anim. Ecol. 69:952-958).
It
is
surprising that in
13
years E548 only grew 42 cm.
It
is expected
that the growth rate
of
large reptiles will decrease towards older
age (e.g., Madsen and Shine, op. cit.),
butE548
is still far from the
largest size recorded for this region (exceeding 500 cm, Rivas et
al., op. cit.) and even further from other literature records. Cursory
evaluation
of
our mark/recapture data suggest that anacondas in
the wild may take more than a decade to reach 320 cm SVL, so
E548 could be in her mid-twenties or perhaps even older.
The harvest
of
anacondas have been present for more than
two decades driven largely by demand for luxury snakeskin
products in the global market (Waller
et
al. 2007. In Henderson
and Powell [eds.], Biology
of
the Boas and Pythons, pp. 340-362.
Eagle Mountain Publishing Company, Eagle Mountain, Utah).
However, rural populations may also be increasing their harvest
in response to changes associated with macroeconomic packages
that are affecting much
of
South America (Rivas 2007. Iguana.
14:
10-21). Nevertheless, a recent three-year study monitored the
experimental harvest
of
wild Eunectes noteus (Yellow Anaconda)
and concluded that harvest could be sustainable based primarily
on high reproductive i:ates, large distribution, and low human
density (Waller et al., op. cit.). However,
if
the extremely slow
growth rate presented here is the norm, we believe that the notion
of
sustainability is suspect in regions with high harvest/mortality
(see Rivas, op. cit.; Rivas et al. 1999. Herpetol. Rev. 30:101;
Rivas 2000. Unpubl. Ph.D. dissertation, University
of
Tennessee.
287 pp.; Rivas et al. 2001. Herpetol. Rev. 32:107-108).
We thank the Wildlife Conservation Society, Zoo de Doue la
Fontaine-France, Miami Metro Zoo,Anaconda Investments LLC,
COVEGAN,
J.
and T. Dunbar, and T. Hughes for assistance.
Submitted by
JESUS
A. RIVAS, Department
of
Math and
Natural Sciences, Somerset Community College, 808 Monticello
Street,Somerset,Kentucky42501,
USA;andSARAHJ.COREY,
Department
of
Evolution, Ecology, and Organismal Biology, The
Ohio State University, 318
W.
12'h
Avenue, Columbus, Ohio
43210, USA.
FARANCIA
ABACURA
(Mud Snake).
PREDATION
. Few re-
cords exist regarding predators
of
Farancia. Palmer and Braswell
(1995. Reptiles
of
North Carolina. University
of
North Carolina
Press, Chapel Hill) report
ed
that American Alligators (Alligator
mississippiensis) and Cottonmouths (Agkistrodon piscivorus)
consumed Farancia abacura and these appear
to
be their only
documented predators. It has been suggested that birds
of
prey
and wading birds predate
mud
snakes (Ernst and Ernst 2004.
The Snakes
of
the United States and Canada. Smithsonian Press,
Washington, D.C.) and birds have been used experimentally to
elicit death feigning (Doody et al. 1996. Herpetol. Rev. 27: 82-83).
However, there are no records
of
birds preying upon Mud Snakes
in
situ.
Herpetological Review 39(4), 2008 469
... Our understanding of the biology of adult Green Anacondas has improved in recent years. There have been comprehensive studies of their mating system (Rivas and Burghardt, 2001;Rivas et al., 2007a), general natural history (Rivas, 2000;Rivas et al., 2007b), conservation and sustainable use (Rivas, 2007(Rivas, , 2010, predation (Rivas et al., 1999Rivas and Owens, 2000), diseases (Calle et al., 1994, foraging (Rivas, 1998(Rivas, , 2004, and demography (Rivas and Corey, 2008), along with notes on field techniques (Rivas et al., 1995;Raphael et al., 1996;Rivas, 2008). Adult anacondas live in shallow, stagnant water that is often covered by aquatic vegetation (Rivas, 2000;Rivas et al., 2007b). ...
... This is true for both juvenile females and most males throughout their lives, but as soon as females reach reproductive size, which is larger than the maximum size obtained by most males, they switch to feeding on mammals and reptiles (Rivas, 2000). Growth rates decline in adulthood; there is a documented case of an adult free-ranging anaconda taking 13 years to grow little more than half a meter (Rivas and Corey, 2008). Adult anacondas may be found in aggregations during the dry season where they apparently gather in cave-like depressions that are exposed in the river banks when the water level drops, or the few ponds that hold water until the wet season returns. ...
... In a long-term study on their ecology, Madsen and Shine (2000) found growth rates between 1 and 1.9 mm/day, far higher than that found in neonatal anacondas. Adult anacondas do have a very slow growth rate, even slower than that of neonates (Rivas and Corey, 2008). ...
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Our knowledge of the biology of neonatal snakes has lagged behind that of adult animals, mostly due to the difficulty of finding and studying neonatal snakes in the wild. Traditional approaches view neonatal reptiles as miniature replicates of their adult counterparts. In this contribution, we present data on the natural history of neonatal Green Anacondas from opportunistic captures in the wild over a 17-year period, as well as from a brief study on captive-born radio-tagged individuals. Both approaches converge in presenting a picture of the ecology of neonatal anacondas showing many similarities between their natural history and that of adult anacondas in spite of the great size difference. The neonates' biology resembles that of adults, especially males, in their preference for birds in their diet, the relative prey size they choose, slow growth rates they experience, low feeding frequency, little mobility, and preference for similar habitats of stagnant, shallow water covered by aquatic vegetation. The conventional wisdom that neonatal reptiles are replicates of their adult counterparts seems to be largely on target in Green Anacondas. © 2016 by the American Society of Ichthyologists and Herpetologists.
... There have been comprehensive studies on the general natural history of the genus Eunectes [22,[33][34][35] including diet [36][37][38][39][40][41][42][43][44][45], diseases [46,47], habitat use and mobility [22,[30][31][32][33]44,45], allometric growth [48,49], and demography [22,50]. On the other hand, the conservation status of anacondas throughout their range is largely unexplored, although Eunectes species are protected from international trade by CITES's Appendix 2 [51][52][53]. ...
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Anacondas, genus Eunectes, are a group of aquatic snakes with a wide distribution in South America. The taxonomic status of several species has been uncertain and/or controversial. Using genetic data from four recognized anaconda species across nine countries, this study investigates the phylogenetic relationships within the genus Eunectes. A key finding was the identification of two distinct clades within Eunectes murinus, revealing two species as cryptic yet genetically deeply divergent. This has led to the recognition of the Northern Green Anaconda as a separate species (Eunectes akayima sp. nov), distinct from its southern counterpart (E. murinus), the Southern Green Anaconda. Additionally, our data challenge the current understanding of Yellow Anaconda species by proposing the unification of Eunectes deschauenseei and Eunectes beniensis into a single species with Eunectes notaeus. This reclassification is based on comprehensive genetic and phyloge-ographic analyses, suggesting closer relationships than previously recognized and the realization that our understanding of their geographic ranges is insufficient to justify its use as a separation criterion. We also present a phylogeographic hypothesis that traces the Miocene diversification of anacondas in western South America. Beyond its academic significance, this study has vital implications for the conservation of these iconic reptile species, highlighting our lack of knowledge about Citation: Rivas, J.; De La Quintana, P.; Mancuso, M.; Pacheco, L.F.; Rivas, G.A.; Mariotto, S.; Salazar-Valenzuela, D.; Baihua, M.T.; Baihua, P.; Burghardt, G.M.; et al.
... However, Ch. angulifer shows relatively low growth rates even in captivity (Tolson 1992;Tolson and Henderson 1993;Morell et al. 1998;Polo and Moreno 2007). Among large boids, free-ranging Green Anacondas also show relatively low growth rates (Rivas and Corey 2008;Rivas et al. 2016). ...
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The Cuban Boa (Chilabothrus angulifer) is a top terrestrial predator in Cuba. References to prey species consumed by this boa date to when the first Europeans arrived in the region more than 500 years ago. However, long-term studies on its trophic ecology do not exist. The scarce and scattered records on its feeding habits indicate that this boa preys on a variety of native and domestic animals. Based on dietary information collected in the field and from the literature, we characterized the diet of this snake and tested four different hypotheses: (1) The Cuban Boa is a generalist predator; (2) the diets of boas in natural and anthropogenic habitats differ; (3) an ontogenetic shift in diet occurs; and (4) foraging strategies used in natural and anthropogenic habitats differ. We identified 49 prey species from 351 prey items obtained from 218 snakes, including 71 items (31 snakes) from the literature. Mammals represented 55% of total prey items consumed, followed by birds (41%) and ectotherms (4%). Chilabothrus angulifer exhibited a narrow niche breadth. However, rather than a trophic specialist, we consider this boa an opportunistic generalist predator, capable of adjusting its diet and foraging behavior according to prey availability and abundance. The diet of Ch. angulifer changed dramatically from mostly native mammals and birds in natural habitats to mostly livestock, pets, and human com-mensals in human-altered habitats. Also, mammals were consumed more frequently in natural habitats, whereas birds dominated the diet of boas associated with anthropogenic habitats. Few ectotherms were consumed in either type of habitat. We observed an ontogenetic shift in diet, but this primarily reflected a trend of consuming larger prey rather than a shift from ectotherms to endotherms as reported for some other boids. In natural habitats, Ch. angulifer used both ambush and active-foraging modes by day and night, whereas in anthropogenic situations, most boas used an active-foraging strategy at night. The frequent consumption of domestic animals by Cuban Boas might be the principal reason for the historical human-wildlife conflict involving this species in rural areas of Cuba.
... al. (2008), Lamonica et. al. (2007), Müller (1970), Petzold (1983) Rivas (1998, 2000, Rivas and Corey (2008), Rivas and Burghardt (2001), Rivas and Owens (2000), Rivas et. al. (1995Rivas et. ...
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A review of the taxonomy of the New World boids finds several genera as currently recognized to be paraphyletic. There are available genus names for those species within genera that have been found to be composite, should they be split to ensure monophyletic genera. The only potential exception to this is within the genus Eunectes Wagler, 1830 as currently recognized. There is a strong argument in favor of splitting the so-called Yellow Anacondas away from the so-called Green Anacondas, at the genus level as a result of clear and consistent differences between the relevant taxa. This paper formalizes this division by taking a conservative position and naming and defining a new subgenus, Maxhoserboa subgen. nov. for the Yellow Anaconda and related species.
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... Predação de conspecíficos é um evento registrado para várias linhagens de serpentes (boídeos, dipsadídeos, elapídeos) e aparentemente é mais frequente em espécies com hábitos alimentares generalistas e ofiófagos (e.g. Engeman et al. 1996, Rivas & Owens 2000, Hartmann & Marques 2005. ...
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Full-text available
The present study reports on food habits of snakes in Espigão do Oeste, Rondônia State (Southwestern Amazonia), Brazil. Snakes were recorded by time constrained search, pitfall traps with drift fences, captures by local inhabitants, and opportunistic sightings. The snakes collected had their stomachs and intestinal contents examined. Information on food habits was obtained for 89 specimens belonging to 31 species. The majority of the 114 items found (stomach contents and field observations) were adult frogs (38%), followed by mammals (16%), lizards (15%), mollusks (13%), birds (5%), and snakes (5%). The majority of snake species from Espigão do Oeste feed on lizards, as in Central Amazonia (Manaus). A smaller proportion of snakes in the Amazonia feed upon frogs in relation to the Pantanal, South and Southeastern Brazil. These differences may be due to greater proportion of Xenodontinae in extra-Amazonian communities, as many snakes in that clade prey upon frogs. Most of the frogs and lizards species recorded in stomach contents snakes are terrestrial, which should be associated with most species of analysed snakes (52%) foraging on the ground.
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Full-text available
Introduction Trophic cascades can produce important effects on a community where some species may have strong effects on other parts of the community up, down the food chain, or both. Top predators are often controlled from the bottom-up by the abundance of their prey base while prey animals are often controlled from the top-down. Studies of trophic interactions in the tropics suggest that the trophic chains are longer because of the high productivity; and because of the high diversity there is abundant intraguild redundancy which results in weak interactions. Methods We studied the effect of bottom-up forces affecting the population of green Anaconda (Eunectes murinus) in the Venezuelan llanos; looking at net primary productivity, precipitation, and the abundance of an important prey item, Capybara (Hydrochaeris hydrochaeris). Results Our data show a strong interaction of these variables on the percentage of Anacondas that reproduce in a given year (here forth breeding ratio). In particular Capybara abundance has a strong effect. Capybara abundance itself is also under strong bottom-up influence determined by precipitation and Net Primary Productivity. Discussion These strong interactions are not what is expected from a tropical ecosystem. We also found an unexpected strong influence of precipitation and primary productivity on Anaconda breeding ratio not related to the abundance of Capybara, likely affecting abundance of other prey or affecting non-trophic variables. This later evidence supports the notion that there is redundancy in tropical food chains and, strong as the effect of Capybara abundance might be, Anacondas do not entirely rely on them.
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