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Abstract

This special issue of Tropical Conservation Science provides a synopsis of nine of the eleven presentations on ungulates presented at the Symposium on Ecology and Conservation of Ungulates in Mexico during the Mexican Congress of Ecology held in November 2008 in Merida, Yucatan. Of the eleven species of wild ungulates in Mexico (Bairds tapir Tapirus bairdii, pronghorn antelope Antilocapra americana, American bison Bison bison, bighorn sheep Ovis canadensis, elk Cervus canadensis, red brocket deer Mazama temama, Yucatan brown brocket Mazama pandora, mule deer Odocoileus hemionus, white-tailed deer Odocoileus virginianus, white-lipped peccary Tayassu pecari and collared peccary Pecari tajacu), studies which concern four of these species are presented: Baird's tapir and the white lipped peccary, which are tropical species in danger of extinction; the bighorn sheep, of high value for hunting in the north-west; and the white-tailed deer, the most studied ungulate in Mexico due to its wide distribution in the country and high hunting and cultural value. In addition, two studies of exotic species, wild boar (Sus scrofa) and red deer (Cervus elaphus), are presented. Issues addressed in these studies are: population estimates, habitat use, evaluation of UMA (Spanish acronym for 'Wildlife Conservation, Management and Sustainable Utilization Units') and ANP (Spanish acronym for 'Natural Protected Areas') to sustain minimum viable populations, and the effect of alien species in protected areas and UMA, all of which allow an insight into ungulate conservation and management within the country.
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Special issue: introduction
Research on ecology, conservation and
management of wild ungulates in Mexico
Sonia Gallina
1
and Salvador Mandujano
1
1
DepartamentodeBiodiversidadyEcologíaAnimal,InstitutodeEcologíaA.C.,km.2.5Carret.Ant.
CoatepecNo.351,CongregacióndelHaya,Xalapa91070,Ver.México.Email:
<sonia.gallina@inecol.edu.mx
>;<salvador.mandujano@inecol.edu.mx>
Received: Received 6 February 2009; Accepted 15 February 2009, Published: 25 May, 2009
Copyright: © Sonia Gallina and Salvador Mandujano. This is an open access paper. We use the
Creative Commons Attribution 3.0 license http://creativecommons.org/licenses/by/3.0/
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Cite this paper as: Galllina, S. and Mandujano, S. 2009. Research on ecology, conservation and
management of ungulates in Mexico. Tropical Conservation Science Vol. 2 (2):116-127. Available
online: www.tropicalconservationscience.org
Abstract
This special issue of Tropical Conservation Science provides a synopsis of nine of the eleven
presentations on ungulates presented at the Symposium on Ecology and Conservation of Ungulates
in Mexico during the Mexican Congress of Ecology held in November 2008 in Merida, Yucatan. Of the
eleven species of wild ungulates in Mexico (Baird´s tapir Tapirus bairdii, pronghorn antelope
Antilocapra americana, American bison Bison bison, bighorn sheep Ovis canadensis, elk Cervus
canadensis, red brocket deer Mazama temama, Yucatan brown brocket Mazama pandora, mule deer
Odocoileus hemionus, white-tailed deer Odocoileus virginianus, white-lipped peccary Tayassu pecari
and collared peccary Pecari tajacu), studies which concern four of these species are presented:
Baird’s tapir and the white lipped peccary, which are tropical species in danger of extinction; the
bighorn sheep, of high value for hunting in the north-west; and the white-tailed deer, the most
studied ungulate in Mexico due to its wide distribution in the country and high hunting and cultural
value. In addition, two studies of exotic species, wild boar (Sus scrofa) and red deer (Cervus
elaphus), are presented. Issues addressed in these studies are: population estimates, habitat use,
evaluation of UMA (Spanish acronym for ‘Wildlife Conservation, Management and Sustainable
Utilization Units’) and ANP (Spanish acronym for ‘Natural Protected Areas’) to sustain minimum
viable populations, and the effect of alien species in protected areas and UMA, all of which allow an
insight into ungulate conservation and management within the country.
Key words: wild ungulates, research needs, conservation, species extinction, Mexico.
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Introduction
Ungulates include the majority of large herbivores on the planet [1]. With the exception of
Antarctica, they are found in nearly all biomes and zoogeographical regions, with human
intervention allowing many species to expand their original geographical boundaries. The
actual number of species varies from author to author because the concept of species is
flexible and is constantly changing depending on the results of genetic and taxonomic
research. The most widely accepted list is that published by Wilson and Reeder [2]. In
general, the Smithsonian Institute recognizes 257 species of modern ungulates. Of these,
at least five species have gone extinct in the last 300 years due to anthropogenic
pressures, and many other species are of critical conservation concern [1].
There are 34 species of ungulates in The Americas (hereinafter America), which represents
13.2% of the ungulate species worldwide (Appendix 1). Of these 34 species, 91% belong
to the order Artiodactyla and the remainder to Perissodactyla. Cervidae is one of the most
represented families within the order Artiodactyla. This family includes 19 species which
correspond to 55.9% of American ungulates. Mazama is the most diverse cervid genus in
South America, represented by seven species [3,4], however, it is also one of the least
known. The families Antilocapridae and Tayassuidae are endemic to America and are
represented by one and three species respectively. Other families are the Camelidae and
Tapiridae. In America, these are represented by two of the four species found worldwide
and three of the four species found worldwide, respectively. Another notable aspect of
American ungulates is the near absence of the Bovidae, the most species diverse ungulate
family (137 species, most of which are found in Africa and Asia [2]). This family is
represented in America by five species, which are confined to North America. Of the 34
species of American ungulates, 10 species are restricted to the Nearctic zoogeographic
region, while 22 species inhabit the Neotropical region. The remaining two species, with
the largest geographical distribution in America are the white-tailed deer (Odocoileus
virginianus) and collared peccary (Pecari tajacu), which inhabit very different vegetation
types in the Nearctic and Neotropics [5,6].
Molecular dating suggests that the family Cervidae originated and radiated in central Asia
during the Late Miocene, and that Odocoileini dispersed to North America during the
Miocene/Pliocene boundary, and underwent an adaptive radiation in South America after
their Pliocene dispersal across the Isthmus of Panama [7]. According to the systematic
relationships and evolutionary history of Neotropical deer, at least eight ancestral forms of
deer invaded South America during the late Pliocene (2.5–3 MYA), and members of the
red brockets had an independent early explosive diversification soon after their ancestor
arrived there, giving rise to a number of morphologically cryptic species. Deer endemic to
the New World fall in two biogeographic lineages: the first one groups Odocoileus and
Mazama americana is distributed in North, Central, and South America, whereas the
second one is composed of South American species only and includes Mazama
gouazoubira. This implies that the genus Mazama is not a valid taxon [3]. Genetic analysis
revealed high levels of molecular and cytogenetic divergence between groups of
morphologically similar species of brockets (Mazama), and suggest a polyphyletic origin.
In particular, Mazama americana showed a striking relationship with several sequences of
Odocoileus i
n contrast to that expected, since this M. americana (now M. temama)
haplotype, from a Mexican origin, was not associated with several Bolivian Mazama
sequences analyzed. This could put forward that this genera is not monophyletic. On the
other hand, these Bolivian Mazama formed a clade with Pudu puda and Ozotoceros
bezoarticus. Likely, an Odocoileus virginianus sequence from the Central area of Colombia
showed a more strong relationship with a North American O. heminonus sequence than
with the other O. virginianus sequences of Colombian origin as well. This could be
explained by means of various different hypotheses. The first is the existence of common
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ancestral haplotypes between both species. Another one is the reiterative hybridization
among both Odocoileus species before the migration of O. virginianus from North America
to South America [8].
Ungulates in Mexico
Eleven ungulate species are found in Mexico (one Perissodactyl species and ten
Artiodactyls species) [9-19], which correspond to 32.4% and 4.3% of ungulate species in
America and worldwide, respectively. The Perissodactyl species is the Baird’s tapir Tapirus
bairdii (Gill, 1865), and the Artiodactyl species are: one species of Antilocapridae, the
pronghorn antelope Antilocapra americana (Ord, 1815); two species of Bovidae, the
American bison Bison bison (Linnaeus, 1758) and the bighorn sheep Ovis canadensis
(Shaw, 1804); five species of Cervidae, elk Cervus canadensis (Erxleben, 1777), the red
brocket Mazama temama (Kerr, 1792), the Yucatan brown brocket Mazama pandora
(Merriam, 1901), the mule deer Odocoileus hemionus (Rafinesque, 1817), and the white-
tailed deer Odocoileus virginianus (Zimmermann, 1780); and two species of Tayassuidae,
the white lipped peccary Tayassu pecari (Link, 1795) and the collared peccary Pecari
tajacu (Linnaeus, 1758).
Baird’s tapir Tapirus bairdii (photo Eduardo Naranjo), Pronghorn antelope Antilocapra
americana (photo Sonia Gallina), American bison Bison bison (photo Sonia Gallina),
Bighorn sheep Ovis canadensis (photo Sergio Alvarez-Cárdenas).
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It is worthy of note that at in all States of Mexico, at least one species of ungulate is found
[5]. For example, five species (pronghorn antelope, bison, bighorn sheep, elk and mule
deer) inhabit the Nearctic region, four species (tapir, red brocket, Yucatan brown brocket
and white lipped peccary) inhabit the Neotropical region, and the remaining two species,
with the widest geographical and ecological distribution (white-tailed deer and collared
peccary), are found throughout almost the country. However, the areas of distribution of
Mexican ungulates have declined markedly and local populations have been eradicated in
some localities. The main causes are uncontrolled hunting, and the loss and
fragmentation of habitat [4]. This has led to the extinction of species like the American
bison and elk in Mexico [11,13], although populations of these have been reintroduced.
Meanwhile, species such as the tapir, bighorn sheep, white lipped peccary and pronghorn
antelope are considered in danger of extinction [9,10,12,18]. With regard to brocket deer,
there is insufficient information to discern their conservation status [14,15]. The deer
genus Odocoileus and collared peccary are not regarded as endangered and their
exploitation is possible under certain restrictions and within the framework of UMA
(Spanish acronym for ‘Wildlife Conservation, Management and Sustainable Utilization
Units’) [17,19]. While the number of studies with these species has increased notably
throughout the country in recent years, there are still significant gaps in our knowledge
[4,20,21].
Wapiti or elk Cervus canadensis (photo Sonia Gallina), Red brocket deer Mazama temama
(photo Rafael Reyna), Yucatan brocket deer Mazama pandora (photo Rosa María González
Marín), Mule deer Odocoileus hemionus (photo Carlos López González).
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Purpose of special issue
In November 2008 the Symposium on Ecology and Conservation of Ungulates in Mexico
was organized during the Mexican Congress of Ecology in Merida, Yucatan. The aim was
to bring together researchers who are working on different groups of ungulates in the
country in order to share recently gained knowledge and to define both the issues of
conservation affecting the different species, and the strategies necessary to address these
issues. During the event, there were eleven presentations concerning seven of the eleven
species of ungulates in Mexico, in addition to two presentations on wild boar and red deer.
As a result of this event, nine of the eleven presentations are extensively presented in this
special issue of the journal Tropical Conservation Science. These studies, carried out in
different parts of the country, address topical issues and allow readers interested in
conservation and management insight into the status of this important group of mammals
in Mexico.
Implications for conservation
Based on the results of these studies, the implications for conservation differ in some
aspects and agree in others, depending on the species in question. In the case of
endangered species such as Baird’s tapir and the white lipped peccary, Naranjo [22] and
Reyna-Hurtado [23] suggest that it is crucial to maintain areas of habitat as large as
possible, avoid fragmentation, increase connectivity between these areas, make plans for
land use involving surrounding communities, and implement actions to reduce the hunting
of these species. As for the bighorn sheep, which is a vulnerable species with permitted
exploitation in special cases, Alvarez-Cardenas et al. [24] emphasize the importance of
intermountain movement of individuals looking for suitable areas for breeding, rearing of
young, feeding, water and genetic exchange, and therefore it is important to maintain and
White-tailed deer Odocoileus
virginianus (photo Alberto González
Gallina), White-lipped peccary
Tayassu pecari (photo Alberto
González Romero) and Collared
peccary Pecari tajacu (photo Alberto
González Romero).
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restore habitat structural elements to enhance the connectivity between isolated
populations.
Regarding the white-tailed deer, Sanchez-Rojas et al. [25] emphasize the importance of
UMA as a complementary strategy for the conservation and sustainable use of this species
in forested areas in the center of the country. Delfin-Alfonso et al. [26] propose a model
for habitat assessment using geographic information systems in order to identify areas of
conservation, management and reintroduction of white-tailed deer in central Veracruz.
This model is also a methodological proposal to assess habitat in other regions of the
country with similar characteristics. On the other hand, Coronel-Arellano et al. [27]
propose to use the standardized vegetation index as a predictive variable of the density of
white-tailed deer in temperate habitat sites, and emphasize the importance of this
procedure as a potential tool for other areas focusing on the conservation and
reintroduction of large carnivores, for which the deer are prey. The work of Mandujano
and Gonzalez-Zamora [28] shows that most UMA do not have the critical size to support
minimum viable populations (MVP) of white-tailed deer, while the Biosphere Reserves,
Areas of Protection of Natural Resources, and Protected Areas of Flora and Fauna, are the
ANP (Spanish acronym for ‘Natural Protected Areas’) which could potentially support the
MVP of this species. They suggest a system of conservation at a regional level in which
ANP and UMA are incorporated, assuming source-sink and archipelago reserve models,
where connectivity can have an important role in the movement of individuals between
populations.
Gallina and Escobedo-Morales [29] suggest connecting UMAs to preserve regional
biodiversity and maintain the viability of wildlife populations. The introduction of exotic
species, such as red deer, is an important alternative at production level but has not
contributed to the conservation of native species and in many cases may have serious
negative consequences. Therefore, strict control of these exotic species is necessary, as
the encouragement of the use and conservation of native wildlife and the revision of the
main conservation objectives of UMA. Finally, Breceda et al. [30] report on wild boar, an
exotic species, and emphasize the potential impacts this animal may have on native
species of ungulates, as they may compete for food and space and cause changes in
habitat and the regeneration processes of endemic plants. Moreover, they constitute a
potential threat to the biodiversity of Biosphere Reserves, which contain a significant
number of endemic species. For these reasons continuous population control is necessary.
Species and research topics not included in this special number
In Mexico, the bison is under special protection and the only wild population is found in a
region that is under evaluation to be protected as a reserve [31]. The pronghorn antelope
is an endangered species in our country but there are some stable populations in different
localities [32]. Mule deer is not an endangered species but some subspecies (O. h.
cerrocensis, O. h. peninsulae y O. h. sheldoni) have severe conservation problems [16].
There are population studies in Durango and Baja California [33-35]. The brocket deer
species are not in danger but are considered fragile [14,15], there are some studies in the
southeast states as Campeche, Quintana Roo, Chiapas and Tabasco [36-38]. Nevertheless
there is a need to do more efforts in order to increase the knowledge of these species
including their systematic, because the phylogenetic origin is not yet clear [3,7,8]. The
other species not treated in this special number is the collared peccary, with a widest
geographical distribution and exploited in Mexico, but with very few ecological studies
[39]. Most of the information we have, has been obtained as a prey in studies related with
felids [40-42].
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Some topics about management and conservation of ungulates that need research efforts
in a short time are:
Analyze the use and sustainable hunting of ungulates in indigenous communities
in areas with high and low hunting pressure [38,43].
Assessing the effectiveness of the UMA for conservation and sustainable use of
ungulates [44,45]. In particular, in tropical forest there is a need to look for
different management strategies [46,47].
Studies on fragmentation, sink-source models and metapopulations from a
landscape perspective [48,49].
Know about the role of ungulates in tropical habitats as structural agents on
vegetation and the consequences of their absence [50].
Genetic and distribution studies of white-tailed deer [51], mule deer [S. Ayala,
personal communication] and brocket deer subspecies [3,7,8].
Analyze the relationship about human population growing, agriculture
technology, cattle ranching, habitat transformation and their effect on
distribution areas of ungulate populations [52-54].
Acknowledgments
We gratefully acknowledge the Mexican Ecological Society for allowing the organization of
the Symposium on Ecology and Conservation of Ungulates in Mexico. Many thanks also go
to Alejandro Estrada, editor of the journal Tropical Conservation Science, for his patience
and interest in this special edition. Finally, thanks go to all the reviewers who kindly
reviewed and helped improved each of the papers in this special issue.
Cited references
[1] Huffman, B. 2008. Ultimate ungulate page, www.ultimateungulate.com, December
3, 2008.
[2] Wilson, D. E. and Reeder, D. A. M. 2005. Mammal Species of the World: A
Taxonomic and Geographical Reference. The Smithsonian Institution Press,
Washington, D. C.
[3] Duarte, J. M. B., González, S. and Maldonado, J. E. 2008. The surprising
evolutionary history of South American deer. Molecular Phylogenetics and Evolution
49:17-22.
[4] Weber, M. and González, S. 2003. Latin America deer diversity and conservation: A
review of status and distribution. Ecoscience 10:443-454.
[5] Hall, E. R. 1981. The Mammals of North America. Second ed. John Wiley and Sons,
New York, 2:601-1181 + 90.
[6] Eisenberg, J.F. 1989. Mammals of the Neotropics: The Northern Neotropics.
University of Chicago Press, x + 449 pp.
[7] Gilbert, C., Ropiquet, A., and Hassanin, A. 2006. Mitochondrial and nuclear
phylogenies of Cervidae (Mammalia, Ruminantia): Systematics, morphology, and
biogeography. Molecular Phylogenetics and Evolution 40:101-117.
[8] Ruiz-García, M., Randi, E., Martínez-Agüero, M. and Alvarez, D. 2007. Phylogenetic
relationships among Neotropical deer genera (Artiodactyla: Cervidae) by means of
DNAmt sequences and microsatellite markers. Revista de Biología Tropical 55:723-
741.
Mongabay.com Open Access Journal - Tropical Conservation Science Vol. 2 (2):116-127, 2009
Tropical Conservation Science | ISSN 1940-0829 | tropicalconservationscience.org
123
[9] March, I.J. and Naranjo, E. J. 2005. Tapir, Tapirus bairdii (Gill, 1865). In: Los
Mamíferos Silvestres de México, Ceballos, G. y Oliva, G. (Eds.), pp. 496-497,
CONABIO y Fondo de Cultura Económica, México, D. F.
[10] Cancino, J. 2005.
Berrendo, Antilocrapa americana (Ord, 1815). In: Los Mamíferos
Silvestres de México, Ceballos, G. and Oliva, G. (Eds.), pp. 502-504, CONABIO y
Fondo de Cultura Económica, México, D. F.
[11] Pacheco, J. 2005. Bisonte americano, Bison bison (Linnaeus, 1758). In: Los
Mamíferos Silvestres de México, Ceballos, G. y Oliva, G. (Eds.), pp. 505-506,
CONABIO y Fondo de Cultura Económica, México, D. F.
[12] Sánchez, O. 2005. Borrego cimarrón, Ovis canadensis (Erxleben, 1777). In: Los
Mamíferos Silvestres de México, Ceballos, G. and Oliva, G. (Eds.), pp. 507-509,
CONABIO y Fondo de Cultura Económica, México, D. F.
[13] Weber, M. and Galindo-Leal, C. 2005. Wapiti, Cervus canadensis (Erxleben, 1777).
In: Los Mamíferos Silvestres de México, Ceballos, G. and Oliva, G. (Eds.), pp. 510-
511, CONABIO y Fondo de Cultura Económica, México, D. F.
[14] Gallina, S. 2005. Temazate, Mazama americana (Erxleben, 1777). In: Los
Mamíferos Silvestres de México, Ceballos, G. y Oliva, G. (Eds.), pp. 512-513,
CONABIO y Fondo de Cultura Económica, México, D. F.
[15] Medellín, R.A. 2005. Venado temazate café, Mazama pandora Merriam, 1901. In:
Los Mamíferos Silvestres de México, Ceballos, G. and Oliva, G. (Eds.), pp. 514-515,
CONABIO y Fondo de Cultura Económica, México, D. F.
[16] Weber, M. and Galindo-Leal, C. 2005. Venado bura, Odocoileus hemionus
(Rafinesque, 1817). In: Los Mamíferos Silvestres de México, Ceballos, G. and Oliva,
G. (Eds.), pp. 515-517, CONABIO y Fondo de Cultura Económica, México, D. F.
[17] Galindo-Leal, C. and Weber, M. 2005. Venado cola blanca, Odocoileus virginianus
(Zimmermann, 1708). In: Los Mamíferos Silvestres de México, Ceballos, G. y Oliva,
G. (Eds.), pp. 517-521, CONABIO y Fondo de Cultura Económica, México, D. F.
[18] March, I. J. 2005. Pecarí de labios blancos, Tayassu pecari (Link, 1795). In: Los
Mamíferos Silvestres de México, Ceballos, G. and Oliva, G. (Eds.), pp. 522-524,
CONABIO y Fondo de Cultura Económica, México, D. F.
[19] March, I. J. and Mandujano, S. 2005. Pecarí de collar, Tayassu tajacu (Linnaeus,
1758). In: Los Mamíferos Silvestres de México, Ceballos, G. and Oliva, G. (Eds.), pp.
524-527, CONABIO y Fondo de Cultura Económica, México, D. F.
[20] Mandujano, S. 2004. Análisis bibliográfico de los estudios de venados en México.
Acta Zoologica Mexicana (n.s.) 20:211-251.
[21] Gallina, S., Mandujano, S. and Delfín-Alfonso, C.A. 2007. Importancia de las áreas
naturales protegidas para conservar y generar conocimiento biológico de las
especies de venados en México. In: Hacia una Cultura de Conservación de la
Biodiversidad Biológica, Halftter, G., Guevara, S. and Melic, A. (Eds.), pp. 187-196,
m3m: Monografías Tercer Milenio vol 6. S.E.A., Zaragoza, España.
[22] Naranjo, E. J. 2009. Ecology and conservation of Baird’s tapir in Mexico. Tropical
Conservation Science 2:140-158. Available online:
www.tropicalconservationscience.org
[23] Reyna-Hurtado, R. 2009. Conservation status of the white-lipped peccary (Tayassu
pecari) outside the Calakmul Biosphere Reserve in Campeche, Mexico: a synthesis.
Tropical Conservation Science 2:159-172. Available online:
www.tropicalconservationscience.org
[24] Alvarez-Cárdenas, S., Galina-Tessaro, P., Días-Castro, S., Guerrero-Cárdenas, I.,
Castellanos-Vera, A. and Mesa-Zavala, E. 2009. Evaluación de elementos
estructurales del hábitat del borrego cimarrón en la Sierra del Mechudo, Baja
California Sur, México. Tropical Conservation Science 2:189-203. Available online:
www.tropicalconservationscience.org
Mongabay.com Open Access Journal - Tropical Conservation Science Vol. 2 (2):116-127, 2009
Tropical Conservation Science | ISSN 1940-0829 | tropicalconservationscience.org
124
[25] Sánchez-Rojas, G., Aguilar-Miguel, C. and Hernández-Cid, E. Estudio poblacional y
uso de hábitat por el Venado Cola Blanca (Odocoileus virginianus) en un bosque
templado de la Sierra de Pachuca, Hidalgo, México. Tropical Conservation Science 2:
204-214. Available online: www.tropicalconservationscience.org
[26] Delfín-Alfonso, C.A., Gallina, S. and López-González, C.A. 2009. Evaluación del
hábitat del venado cola blanca utilizando modelos espaciales y sus implicaciones
para el manejo en el centro de Veracruz, México. Tropical Conservation Science 2:
215-228. Available online: www.tropicalconservationscience.org
[27] Coronel-Arellano, H., López González, C.A. and Moreno Arzate, C.N. 2009.
¿Pueden las variables de paisaje predecir la abundancia de venado cola blanca? El
caso del noroeste de México. Tropical Conservation Science 2:229-236. Available
online: www.tropicalconservationscience.org
[28] Mandujano, S. and González-Zamora, A. 2009. Evaluation of natural conservation
areas and wildlife management units to support minimum viable populations of
white-tailed deer in Mexico. Tropical Conservation Science 2:237-250. Available
online: www.tropicalconservationscience.org
[29] Gallina, S. and Escobedo-Morales, L.A. 2009. Análisis sobre las Unidades de
Manejo (UMAs) de ciervo rojo (Cervus elaphus Linnaeus, 1758) y wapiti (Cervus
canadensis Linnaeus, 1758) en México: problemática para la conservación de los
ungulados nativos. Tropical Conservation Science 2:251-265. Available online:
www.tropicalconservationscience.org
[30] Breceda, A., Arnaud, G., Álvarez-Cárdenas, S., Galina-Tessaro, P. and Montes-
Sánchez, J. 2009. Evaluación de la Población de Cerdos Asilvestrados (Sus scrofa) y
su Impacto en la Reserva de la Biosfera Sierra La Laguna, Baja California Sur,
México. Tropical Conservation Science 2:173-188. Available online:
www.tropicalconservationscience.org
[31] Ceballos, G. and Oliva, G. (Eds.). 2005. Los Mamíferos Silvestres de México,
CONABIO y Fondo de Cultura Económica, México, D.F.
[32] Medellín, R.A., Manterola,C., Valdéz, M., Hewitt, D.G., Doan-Crider, D. and
Fulbright, T.E. 2005. History, ecology and conservation of the pronghorn antelope,
bighorn sheep, and black bear in Mexico. Pp. 387-404, in: Cartron, J.E., Ceballos,
G., and Felger, R.E. (Eds.), Biodiversity, Ecosystems, and Conservation in Northern
Mexico. Oxford University Press,
[33] Sanchez-Rojas, G., and Gallina, S. 2000. Factors Affecting Habitat Use by Mule
Deer (Odocoileus hemionus) in the Central Part of the Chihuahua Desert, México: an
Assessment with Univariate and Multivariate Methods. Ethology, Ecology and
Evolution 12:405-417.
[34] Gallina, S., Galina-Tessaro and Álvarez-Cárdenas, S. 1991. Mule deer density and
pattern distribution in the pine-oak forest at the Sierra de la Laguna in Baja
California Sur. Ethology, Ecology and Evolution 3:27-33.
[35] Pereza, P.I. 2007. Análisis Reproductivo de la Población de Venado Bura
(Odocoileus hemionus fuliginatus) en Áreas Circundantes a El Rosario, Baja
California, México: Consideraciones para su Manejo, Conservación y
Aprovechamiento. Tesis de Maestría en Ciencias. Universidad Autónoma de Baja
California.
[36] Weber, M. 2005. Ecology and conservation of sympatric tropical deer populations
in the Greater Calakmul Region, Campeche, Mexico. Dissertation, Durham
University, Durham, United Kingdom.
[37] Gonzalez-Marin, R., Gallina, S., Mandujano, S. and Weber, M. 2008. Densidad y
distribución de ungulados silvestres en la Reserva Ecológica El Edén, Quintana Roo,
México. Acta Zoológica Mexicana (n.s.)
24: 73-93.
Mongabay.com Open Access Journal - Tropical Conservation Science Vol. 2 (2):116-127, 2009
Tropical Conservation Science | ISSN 1940-0829 | tropicalconservationscience.org
125
[38] Naranjo, E.J., Bolaños, J.E., Guerra, M.M. and Bodmer, R.E. 2004b. Hunting
sustainability of ungulates populations in the Lacandon forest, México. In: People in
Nature: Wildlife Conservation in South and Central America, Silvus, K.M., Bodmer,
R.E. and Fragoso, J.M. (eds.), pp. 324-343. Columbia University Press, New York.
[39] Mandujano, S. 1999. Variation in herds size of collared peccaries in a mexican
tropical forest. The Southwestern Naturalist 44:199-204.
[40] Aranda, M. and Sánchez-Cordero, V. 199
6. Prey spectra of jaguar (Panthera onca)
and puma (Puma concolor) in tropical forests of Mexico. Studies on Neotropical
Fauna and Environment 31:65-67.
[41] Núñez, R., Miller, B. and Lindzey, F. 2000. Food habits of jaguars and pumas in
Jalisco, Mexico. Journal of Zoology 252:373-379.
[42] Rosas-Rosas, O.C., Valdez, R., Bender, L.C. and Daniel, D. 2003. Food habits of
pumas in northwestern Sonora, Mexico. Wildlife Society Bulletin 31: 528-535.
[43] Reyna-Hurtado, R. and Tanner, G.W. 2
005. Habitat preferences of ungulates in
hunted and nonhunted areas in the Calakmul Forest, Campeche, Mexico. Biotropica
37:676-685.
[44] Sisk, T.D., Castellanos, A.E. and Koch, G.W. 2007. Ecological impacts of wildlife
conservation units policy in México. Ecological Environment 5: 209-212.
[45] Valdez, R., Guzmán-Aranda, J.C., Abarca, J.C., Tarango-Arámbula, L.A. and
Clemente-Sánchez, F. 2006. Wildlife Conservation and Management in Mexico
Wildlife Society Bulletin 34:270-282.
[46] Weber, M., García-Marmolejo, G. and Reyna-Hurtado, R. 2006. The tragedy of the
commons: wildlife management units in southeastern México. Wildlife Society
Bulletin 34: 1480-1488.
[47] García-Marmolejo, G., Escalona-Segura, G., and Der Wal, H.V. 2008. Multicriteria
evaluation of wildlife management units in Campeche, Mexico. Journal of Wildlife
Management 72:1194-1202.
[48] Naranjo, E.J. and Bodmer, R.E.
2007. Source-sink systems of hunted ungulates in
the Lacandon Forest, Mexico. Biology Conservation 138:412-420.
[49] Sanchez-Rojas, G. and Gallina, S. 2007. Metapoblaciones, el reto en la biología de
la conservación: el caso del venado bura en el Bolsón de Mapimí. In: Tópicos en
Sistemática, Biogeografía, Ecología y Conservación de Mamíferos, Sanchéz-Rojas, G.
and Rojas-Martínez, A. (eds.), pp. 115-124, Universidad Nacional del Estado de
Hidalgo, México.
[50] Dirzo, R. and Miranda, A. 2000. Contemporary Neotropical defaunation and forest
structure, function and diversity –a sequel to John Terborgh. Conservation Biology
4:444-447.
[51] Logan-López, K, Cienfuegos, E., Sifuentes-Rincón, A.M., González-Paz, M.,
Clemente-Sánchez, F., Mendoza, G. and Taranfo, L.A. 2007. Patrones de variación
genética en cuatro subespecies de venado cola blanca del noreste de México.
Agrociencia 41:13-21.
[52] Peres, C.A. 2002. Synergistic Effects of Subsistence Hunting and Habitat
Fragmentation on Amazonian Forest Vertebrates. Conservation Biology 15:1490-
1505.
[53] Escamilla, A., Sanvicente, M., Sosa, M. and Galindo-Leal, C. 2000. Habitat mosaic,
wildlife availability, and hunting in the tropical forest of Calakmul, Mexico.
Conservation Biology 14:1592-1601.
[54] Naughton-Treves, L., Mena, J.L., Treves, A., Alvarez, N. and Ra
deloff, V.C. 2002.
Wildlife survival beyond park boundaries: the impact of slash-and-burn agriculture
and hunting on mammals in Tambopata, Peru. Conservation Biology 17:1106-1117.
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Appendix 1. Wild ungulates living in the American continent, according to Wilson and
Reeder [2]. * Indicates species in Mexico.
Orden Perissodactyla Owen, 1848
Familia Tapiridae Gray, 1821
Tapirus Brisson, 1762
1. * Tapirus bairdii (Gill, 1865) Baird's tapir, Central American tapir
2. Tapirus pinchaque (Roulin, 1829) Mountain tapir
3. Tapirus terrestris (Linnaeus, 1758) South America tapir, Brazilian tapir,
lowland tapir
Orden Artiodactyla Owen, 1848
Familia Tayassuidae Palmer, 1897
Catagonus Ameghino, 1904
4. Catagonus wagneri (Rusconi, 1930) Chacoan peccary
Pecari Reinchenbach, 1835
5. * Pecari tajacu (Linnaeus, 1758) Collared peccary, javelina
Tayassu G. Fisher [von Waldheim], 1814
6. * Tayassu pecari G. Fisher [von Waldheim], 1814 White-lipped peccary
Familia Camelidae Gray, 1821
Lama G. Cuvier, 1800
7. Lama glama (Linnaeus, 1758) Llama, guanaco
Vicugna Lesson, 1842
8. Vicugna vicugna (Molina, 1782) Vicuña
Familia Cervidae Goldfuss, 1820
Subfamilia Capreolinae Brookes, 1828
Alces Gray, 1821
9. Alces americanus (Clinton, 1822) American moose
Blastocerus Wagner, 1844
10. Blastocerus dichotomus (Illiger, 1815) Marsh deer
Hippocamelus Leuckart, 1816
11. Hippocamelus antisensis (d’Orbigny, 1834) Peruvian guemal, taruca
12. Hippocamelus bisulcus (Molina, 1782) Patagonian huemul, South Andean
huemul
Mazama Rafinesque, 1817
13. Mazama americana (Erxleben, 1777) South American Red brocket
14. Mazama bororo Duarte, 1996 Sao Paulo Bororo, small red brocket
15. Mazama bricenii Thomas, 1908 Merida Brocket, Grey dwarf brocket
16. Mazama chunyi Hershkovitz, 1959, Dwarf brocket
17. Mazama gouazoubira G. Fisher [von Waldheim], 1814, Brown brocket
18. Mazama nana (Hensel, 1872) Lesser brocket
19. * Mazama pandora Merriam, 1901 Yucatan brown brocket
20. Mazama rufina (Pucheran, 1851) Ecuator, Little red brocket
21. * Mazama temama (Kerr, 1792) Central American, Mexican red brocket
Odocoileus Rafinesque, 1832
22. * Odocoileus hemionus (Rafinesque, 1817) Mule deer
23. * Odocoileus virginianus (Zimmermann, 1780) White-tailed deer
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Ozotoceros Ameghino, 1891
Ozotoceros bezoarticus (Linnaeus, 1758) Pampas deer
Pudu Gray, 1852
25. Pudu mephistophiles (de Winton, 1896) Northern pudu
26. Pudu puda (Molina, 1782) Southern pudu
Rangifer C. H. Smith, 1872
27. Rangifer tarandus (Linnaeus, 1758) Caribou, reindeer
Subfamilia Cervinae Goldfuss, 1820
Cervus Linnaeus, 1758
28. * Cervus elaphus Linnaeus, 1758 Red deer, wapiti, American elk
Familia Antilocapridae Gray, 1866
Antilocapra Ord, 1818
29. * Antilocapra americana (Ord, 1815) Pronghorn
Familia Bovidae Gray, 1821
Subfamilia Bovinae Gray, 1821
Bison H. Smith, 1827
30. * Bison bison (Linnaeus, 1758) American bison
Subfamilia Caprinae Gray, 1821
Oreamnos Rafinesque, 1817
31. Oreamnos americanus (de Blainville, 1816) Rocky Mountain goat
Ovibos de Blainville, 1816
32. Ovibos moschatus (Zimmermann, 1780) Muskox
Ovis Linnaeus, 1758
33. * Ovis canadensis Shaw, 1804 Bighorn sheep
34. Ovis dalli Nelson, 1884 Dall's sheep
Cervus canadensis (Erxleben, 1777) according to other authors. For a discussion in this
aspect, see Gallina and Escobedo-Morales [29] in this number.
Reproduction of artistic painting “Deer”. Mixed
technique on canvas, 110 x 90 cm, by Salvador
Mandujano Rodríguez, 2007.
... Differences were obtained for the usable phytomass in each of the vegetation types, in favor of the rainy season over the dry season, because of the higher precipitation and temperatures favoring vegetative growth in this annual period, allowing higher primary productivities to be reached (Morley, 1987, Winograd, 1995, Cantú, 2002, Ramírez, 2004, Villarreal, 2006, Gallina & Mandujano, 2009 It is also recommended to continue conducting carrying capacity studies, year after year, to determine changes in primary productivity and establish a management program aimed at improving the habitat in its four components: water, food, cover and space. ...
... Se obtuvieron diferencias para la fitomasa aprovechable en cada uno de los tipos de vegetación, a favor de la época de lluvias sobre la de estiaje, consecuencia de la mayor ocurrencia de precipitaciones y temperaturas, que favorecen en ese período anual el crecimiento vegetativo, permitiendo se alcancen mayores productividades primarias (Morley, 1987, Winograd, 1995, Cantú, 2002, Ramírez, 2004, Villarreal, 2006, Gallina & Mandujano, 2009). La comparación con los resultados de coeficientes de agostadero obtenidos en el Parque Estatal Flor del Bosque y lo recomendado por COTECOCA, indica que el bosque de pino-encino puede soportar el incremento de venados, para el matorral-pastizal los valores indican reducir las unidades animales para obtener una K estable. ...
Article
Full-text available
The habitat carrying capacity (K) for white-tailed deer (Odocoileus virginianus) in General Lázaro Cárdenas del Río “Flor del Bosque” State Park (FBSP), a Protected Natural Area (PNA) in the state of Puebla, Mexico, was evaluated. This PNA has three vegetation types: oak forest, mixed forest, and scrub-grassland. Phytomass samples were taken in 500-meter-long transects at two times of the year (two for each vegetation type), in the rainy and dry seasons, using Guevara's Forage Balancemethodology and Cantú's formula for the calculation of phytomass production. Differences were obtained for the usable phytomass in each of the vegetation types, in favor of the rainy season (P < 0.05) over the dry season, due to the higher precipitation and temperature that favor plant growth during that period of the year, which allows greater primary productivity. The results of K in number of hectares (ha) per animal unit (AU) were 2.48 ha·AU-1 for oak forest and 10.25 ha·AU-1 for scrub-grassland, which differ from the data established by the COTECOCA grazing coefficients, which assume values of 9.77 ha·AU-1 for oak forest and 8.80 ha·AU-1 for scrub-grassland. In the case of mixed forest, there are no data on grazing coefficients reported by COTECOCA; however, this presents a value of 9.10 ha·AU-1. These data allow us to increase the number of white-tailed deer individuals and establish a 1:1 ratio with the cattle-deer binomial to develop correct management in case of establishing a diversified livestock model for areas adjacent to General Lázaro Cárdenas del Río “Flor del Bosque” State Park
... The Central American Red Brocket, Mazama temama (Erxleben, 1777) is a deer species that has been targeted by illegal hunters for local commercial purposes or as a source of protein (Leopold 1959;Gallina and Mandujano 2009), as well as for its habitat (Gallina and Mandujano 2009;Bello-Gutiérrez et al. 2010). Even so, this deer species is considered Data Deficient by IUCN (Bello et al. 2016). ...
... The Central American Red Brocket, Mazama temama (Erxleben, 1777) is a deer species that has been targeted by illegal hunters for local commercial purposes or as a source of protein (Leopold 1959;Gallina and Mandujano 2009), as well as for its habitat (Gallina and Mandujano 2009;Bello-Gutiérrez et al. 2010). Even so, this deer species is considered Data Deficient by IUCN (Bello et al. 2016). ...
Article
Full-text available
Anthropogenic threats have increasingly isolated the populations of Mazama temama (Erxleben, 1777) and limited the gene flow in this species. Knowledge of the phylogeographic structure of this species is therefore essential for its conservation. Thus, in this study, we describe the phylogeographic structure of two M. temama populations of Veracruz and Oaxaca, Mexico. We sequenced the D-Loop region of the mitochondrial DNA of 16 individuals, in order to estimate the diversity and genetic differentiation ( F ST ), Tajima’s D index, "Mismatch distribution" test; a phylogram and a haplotype network was constructed and we performed multidimensional scaling analysis to test the hypothesis of association between geographic distance and genetic diversity. The haplotypic and nucleotide diversity was high, indicating divergent populations ( F ST = 0.223), while the Tajima’s D index (-1,03300; P > 0.10) determined disequilibrium in the D-Loop region, derived from a population expansion that was evidenced in the "Mismatch distribution" test and confirmed with the haplotype network in the form of a star. Four lineages were identified in the phylogram (Veracruz n = 3, Oaxaca n = 1), evidencing geographic and reproductive isolation between the two populations. This was confirmed by the multidimensional scaling analysis, which evidenced recent evolutionary divergence between the populations analyzed, which are considered evolutionary units of conservation.
... The Central American Red Brocket, Mazama temama (Erxleben, 1777) is a deer species that has been targeted by illegal hunters for local commercial purposes or as a source of protein (Leopold 1959;Gallina and Mandujano 2009), as well as for its habitat (Gallina and Mandujano 2009;Bello-Gutiérrez et al. 2010). Even so, this deer species is considered Data Deficient by IUCN (Bello et al. 2016). ...
... The Central American Red Brocket, Mazama temama (Erxleben, 1777) is a deer species that has been targeted by illegal hunters for local commercial purposes or as a source of protein (Leopold 1959;Gallina and Mandujano 2009), as well as for its habitat (Gallina and Mandujano 2009;Bello-Gutiérrez et al. 2010). Even so, this deer species is considered Data Deficient by IUCN (Bello et al. 2016). ...
Preprint
Citation: Serna-Lagunes R, Romero-Ramos DK, Delfín-Alfonso CA, Salazar-Ortiz J (2021) Phylogeography of the Central American red brocket, Mazama temama (Artiodactyla, Cervidae) in southeastern Mexico. Neotropical Biology and Conservation @(@): 1-@. https://doi. Abstract Anthropogenic threats have increasingly isolated the populations of Mazama temama (Erxleben 1777) and limited the gene flow in this species. Knowledge of the phylogeographic structure of this species is therefore essential for its conservation. Thus, in this study, we describe the phylogeographic structure of two M. temama populations of Veracruz and Oaxaca, Mexico. We sequenced the D-Loop region of the mitochondrial DNA of 16 individuals, in order to estimate the diversity and genetic differentiation (F ST), Tajima's D index, Mismatch distribution test; a phylogram and a haplotype network was constructed and we performed multidimensional scaling analysis to test the hypothesis of association between geographic distance and genetic diversity. The haplotypic and nucleotide diversity was high, indicating divergent populations (F ST = 0.223), while the Tajima's D index (-1,03300; P > 0.10) determined disequilibrium in the D-Loop region, derived from a population expansion that was evidenced in the Mismatch distribution test and confirmed with the haplotype network in the form of a star. Four lineages were identified in the phylogram (Veracruz n = 3, Oaxaca n = 1), evidencing geographic Neotropical Biology and Conservation @(@): 1-@ (2021) Ricardo Serna-Lagunes et al. 2 and reproductive isolation between the two populations. This was confirmed by the multidimensional scaling analysis, which evidenced recent evolutionary divergence between the populations analyzed, which are considered evolutionary units of conservation.
... En este sentido, se ha señalado que la composición de la dieta de los venados cola blanca es variable, pues depende de los recursos que dispone en un ecosistema específico (Beltrán & Díaz, 2017), del grado de conservación del ecosistema y de la estructura y composición de la vegetación. Con base en lo anterior, conocer la diversidad de las especies de plantas y su nivel de importancia es esencial para la planificación del manejo y preservación de los ecosistemas donde vive el venado cola blanca (Gallina & Mandujano, 2009). ...
Article
Full-text available
El objetivo fue conocer la contribución de la diversidad florística de la selva baja inundable (SBI) y la selva mediana subperennifolia (SMS) en la composición botánica de la dieta del venado cola blanca. Se calcularon los índices de valor de importancia (IVI) de las especies, el índice de Margalef (Dmg) y el índice de Shannon (H´), así como la composición botánica de la dieta. La mayor diversidad se encontró en la SMS (H’ = 3.96-3.99; Dmg = 12.11-12.17), comparada con SBI (H’ = 3.80; Dmg = 10.51), y se identificaron 75 especies consumidas por los venados. La dieta del venado se relaciona con un mayor IVI de las especies. Las principales especies en la dieta fueron Cladium mariscus subsp. jamaicense, Thevetia ahouai, Byrsonima bucidifolia, Machaerium cirrhiferum y Dalbergia glabra. Se concluye que la alta diversidad de especies de las selvas tropicales provee una elevada oferta alimenticia a los venados cola blanca, predominando el consumo de especies de las familias Fabaceae, Cyperacea, Rubiaceae y Malvaceae.
... En México, la mayoría de las subespecies de venado cola blanca se distribuye en regiones tropicales, aunque sujetas a alguna modalidad de aprovechamiento; situación que obliga al desarrollo de planes de manejo específicos para cada eco-región. Esta necesidad también obliga a prestar atención a la deficiencia de conocimiento biológico de venados en zonas tropicales, como el patrón reproductivo, uso de hábitat y dieta, entre otros (Vaughan 1994;Gallina y Mandujano 2009; Vishnu-Savanth y Saseendran 2012). ...
Article
Full-text available
Objetivo: analizar la relación entre el nivel de testosterona en heces fecales y el ciclo de las astas, así como determinar el período reproductivo del venado cola blanca (O. v. veraecrucis) en función del hábitat de cuatro Unidades de Manejo para la Conservación de Vida Silvestre (UMA) de la región Huasteca de Veracruz y San Luis Potosí, México. Método: El estudio se realizó en cuatro ranchos ganaderos registrados como UMA, ubicados en los estados de Veracruz y San Luis Potosí, en la región Huasteca de México. Se evaluaron veintisiete muestras fecales y ciento noventa y dos imágenes fotográficas de machos de venado cola blanca para identificar el patrón reproductivo anual. Las muestras e imágenes se recolectaron entre febrero de 2015 y julio de 2016. La concentración de testosterona en heces se determinó mediante pruebas ELISA. Se realizaron análisis estadísticos de regresión lineal y correlación para identificar la relación de la concentración de testosterona con el crecimiento promedio de las astas, de escalamiento multidimensional no métrico para la ordenación de los valores de concentración de testosterona observados, etapa de crecimiento de las astas y variables ambientales. Para agrupar los meses en que los animales presentan características reproductivas similares se aplicó un análisis de k-medias. Resultados: Fue posible identificar una relación positiva entre la variación anual de los niveles de testosterona y las etapas del ciclo de astas; las menores concentraciones hormonales ocurrieron de marzo a junio y coincidieron con la muda y crecimiento de astas nuevas, permitiendo identificar este lapso como no reproductivo, mientras que, entre julio y febrero el nivel de testosterona se mantuvo elevado, coincidiendo con la presencia de astas osificadas y libres de terciopelo, indicador de actividad reproductiva en los machos.
... En México, la mayoría de las subespecies de venado cola blanca se distribuye en regiones tropicales, aunque sujetas a alguna modalidad de aprovechamiento; situación que obliga al desarrollo de planes de manejo específicos para cada eco-región. Esta necesidad también obliga a prestar atención a la deficiencia de conocimiento biológico de venados en zonas tropicales, como el patrón reproductivo, uso de hábitat y dieta, entre otros (Vaughan 1994;Gallina y Mandujano 2009; Vishnu-Savanth y Saseendran 2012). ...
Article
Full-text available
... Our results show that the studied sample of O. virginianus presents a genetic diversity that has not been modified by historical demographic processes such as population expansions (Rogers and Harpending 1992;Rogers et al. 1996). However, the pressure of clandestine hunting and legal hunting of the specie in Mexico (SEMARNAT 2013), its ecology and management (Gallina and Mandujano 2009), habitat fragmentation, poaching, consumption by local communities, and predators (Mandujano 2011;Gallina-Tessaro et al. 2019) are constant pressures on the populations of this species. This decreases the effective size of the mating population in wild populations (Mandujano and González-Zamora 2009), thus only a few lineages go on to the next generation while other lineages go extinct or are less frequent within the population (Rogers et al. 1996;Vázquez-Domínguez 2002). ...
Book
Although all living beings modify their environment, human beings have acquired the ability to do so on a superlative space-time scale. As a result of industrialization and the use of new technologies, the anthropogenic impact has been increasing in the last centuries, causing reductions in the sizes or the extinction of numerous wild populations. In this sense, from the field of conservation genetics, various efforts have been made in recent decades to provide new knowledge that contributes to the conservation of populations, species, and habitats. In this book, we summarize the concrete contributions of researchers to the conservation of the Neotropical mammals using Molecular Ecology techniques. The book is divided into three major sections. The first section provides an up-to-date review of the conservation status of Neotropical mammals, the applications of the molecular markers in its conservation, and the use of non-invasive and forensic genetic techniques. The second and third sections present, respectively, a series of case studies in various species or taxonomic groups of Neotropical mammals.
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Background. The red temazate deer (Mazama temama, Artiodactyla: Cervidae) is a deer with ecological, cultural and economic importance, but its density and habitat characteristics in National Parks are unknown. Objective. To estimate the track index as an indirect measure of density and describe the vegetation characteristics of the habitat of M. temama in the town of Zapoapan, Parque Nacional Cañón del Río (PNCRB), Veracruz, Mexico. Methodology. During January to October 2021, eight transects were established to record tracks, phototraps were installed to determine their presence, and Canfield lines were used to describe the vegetation in areas with the presence of the species. Results. Twenty-three tracks of M. temama were recorded: nine tracks (39%), six excreta (26%), three foraging tracks (13%), three stalls (13%) and two photocaptures (8%), equivalent to an index tracks of 0.57 individuals/ha or 2.2 ha/individual, low density compared to other reports of the species. The habitat presented a richness of 19 species of plants, the shrubs being more abundant (36%) than the herbaceous and arboreal (represented by 32% each); the tree layer was dominant in terms of height and diameter. Implications. These results suggest that the habitat does not have sufficient diversity of resources to maintain a dense population of M. temama. Conclusion. The population density of M. temama in the PNCRB was low associated with a restricted carrying capacity in the study area, so actions must be taken towards the conservation and sustainable use of the population of this species. RESUMEN Antecedentes. El venado temazate rojo (Mazama temama, Artiodactyla: Cervidae) es un cérvido con importancia ecológica, cultural y económica, pero no se conoce sobre su densidad y las características del hábitat en Parques Nacionales. Objetivo. Estimar el índice de rastros como una medida indirecta de la densidad y describir las características de la vegetación del hábitat de M. temama en la localidad de Zapoapan, Parque Nacional Cañón del †
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p> Background. The effects of climate change are increasingly altering patterns of precipitation, temperature increase and longer droughts, which directly impacts the quality of habitat and resources for the maintenance of wildlife populations. Objective. To design and test a management area that will help to reduce wildlife vulnerability during the critical dry season. Methodology. In Wildlife Management Unit (UMA) “Cano Cruz”, in Campeche, Mexico, was evaluated a management plot for wildlife maintenance during dry season (December 2014- June 2015). The management plot had an area of three hectares, providing a water troughs and food resources such as corn, sorghum, pumpkin, among others. At the same time, he worked at an adjacent area of preserved vegetation (control site), five camera traps at both sites were installed for the monitoring of birds and mammals. To establish differences in the presence and use of water and food resources, the Relative Abundance Index was estimated monthly and several statistical tests were applied (Shapiro-Wilk, t-Student, Mann-Whitney U and Square Chi). Results. In the site of preserved vegetation, 74 individuals of three species of birds and 135 individuals of eight mammal’s species were registered, while management plot, 2,575 individuals of 24 bird species and 1,033 individuals of 14 mammal species were recorded. The management plot proved to be an important site during dry season, to maintenance of wildlife species, such as Ocellated Turkey ( Meleagris ocellata ), White-winged Dove ( Zenaida asiatica ), Melodious Blackbird ( Dives dives ), Yucatán Brown Brocket ( Mazama pandora ), White-nosed Coati ( Nasua narica ) and Raccoon ( Procyon lotor ). Conclusion. In the face of higher temperatures and increasingly prolonged droughts in the Yucatan Peninsula, the management plot constitutes an important alternative to implement in community territories, managed under the UMA scheme, since it reduces vulnerability of priority species of birds and mammals.</p
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In Mexico four species of native deer exist: the white-tailed deer (Odocoileus virginianus), the mule deer (O. hemionus), the red brocket deer (Mazama temama) and the brown brocket deer (M. pandora). Unfortunately, the distribution areas of deer populations have diminished notably in the country as a whole, and some local populations have even become extinct, so it is urgent to design alternatives and management strategies for their conservation and appropriate use. One of the best strategic options for the conservation of deer in Mexico lies with the protected natural areas (ANPs), where it is possible to find deer populations which have been less severely affected than in unprotected areas. Here we analyze the importance ANPs have as places that generate biological information on deer, and in particular we lay the stress on the role that the Instituto de Ecología A. C. has played in the research and development of human resources. It was found that the least studied species were the brocket deer and the mule deer, while the white-tailed deer is the most studied species, with 75% of the total research. Five of the country’s 14 subspecies of white-tailed deer have drawn the most attention: O. v. texanus, O. v. couesi, O. v. sinaloae, O. v. mexicanus and O. v. yucatanensis. However, only 17 protected natural areas have generated information on any of the species. The Instituto de Ecología A. C. has contributed 38.5% of deer research in the country. Finally, we can conclude that protected natural areas play a decisive role in the generation of biological information on Mexico’s deer.
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Because the shape of Mexico resembles an upright funnel, most of the country’s land surface area is in the north. A west-to-east cross-section of the country at around 25º N latitude would show the plains and mountains of the Baja California penin-sula, coastal Sonoran plains, Sierra Madre Occiden-tal, Mexican Plateau, Sierra Madre Oriental, and Gulf coastal plains (see chapter 1). This topographi-cally intricate landscape encompasses a wide vari-ety of habitats for wildlife, including montane oak and conifer woodlands and forests, grasslands, and extensive desert regions with plains and often sparsely vegetated peaks.
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At the Calakmul Biosphere Reserve in Campeche, Mexico, the prey spectra of sympatric jaguars (Panthera onca) and pumas (Puma concolor) were studied by examination of their scats. 10 vertebrate species were identified for jaguars and 7 for pumas, mainly mammals and some birds. Based on these diet analyses, we conclude that jaguars and pumas coexist at Calakmul by means of different food habits.
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La generación de información sobre la abundancia de venado cola blanca (Odocoileus virginianus) se ha obtenido a nivel local, lo cual reduce su utilidad para tomar decisiones de manejo y conservación a nivel de paisaje. Nuestro objetivo fue generar un índice predictivo regional para estimar la abundancia de venado cola blanca utilizando imágenes de satélite. La información de campo se generó a partir de estudios locales en dos sitios en el noroeste de México, el primer sitio se ubica en la Sierra de San Luís en el municipio de Agua Prieta, Sonora y el segundo se encuentra ubicado en la Sierra Los Pavos, en el municipio de Sahuaripa, Sonora; de acuerdo a sus características el primer sitio es templado y el segundo es tropical. La densidad de venado cola blanca se calculó por medio de transectos lineales para el conteo de grupos fecales. Se encontró una relación significativa entre el valor de índice de vegetación normalizado (análisis que se deriva de la reflectancia del espectro electromagnétic entre la biomasa verde y su firma espectral; NDVI) y la abundancia de venado cola blanca para una de las localidades muestreada; sin embargo, para la otra localidad no se encontró una relación significativa entre las variables. El NDVI predice la abundancia en el sitio templado y no en el tropical. Al parecer esta relacionado a variables antropogénicas mas que de paisaje. Es posible utilizar el NDVI para identificar áreas de reintroducción para poblaciones de venado cola blanca en sitios templados del Noroeste de México.