Journal of
Threatened Taxa | www.threatenedtaxa.org | 26 May 2018 | 10(6):
11703–11709
Home range and spatial
organization by the Hoary Fox Lycalopex vetulus(Mammalia: Carnivora: Canidae):
response to social disruption of two neighboring pairs
Julio C. Dalponte1, Herson S. Lima 2, Stuart Klorfine 3 & Nelton C. da Luz4
1 Instituto para a Conservação dos Carnívoros Neotropicais(PRÓ-CARNÍVOROS), Avenida Horácio Neto, 1030, Parque Edmundo Zanoni, 12945-010, Atibaia, São Paulo, Brasil
2 Universidadedo Estado de Mato Grosso(UNEMAT), Campus de Nova Xavantina, Av. Expedição Roncador Xingu, Nova Xavantina, Mato Grosso 78690-000, Brasil
3 SQN 215, BlocoB, 505, 70874-020, Brasília DF, Brasil
4 Instituto Nacional de Pesquisas Espaciais (INPE)-
Centro Regional da Amazônia, Parquede Ciência e Tecnologia do Guamá, Avenida Perimetral, 2651, 66077-830, Belém,Pará, Brasil
1 jcdalponte@hotmail.com (corresponding
author), 2 hersonlima@hotmail.com; 3 sklorfine@hotmail.com,4 neltonluz@msn.com
Abstract: The Hoary Fox Lycalopex vetulus, is a small omnivore-insectivore canidinhabiting open environments/areas of the Brazilian savannah, whose spatial
organization and territoriality is still unknown. Space use and social organization of two
breeding pairs with adjacent home ranges were determined through radio tracking
from October 2002 to April 2003 in a mosaic of cultivated pastures and Cerrado vegetation in eastern Mato Grosso, Brazil. Home ranges were 140–299 ha in size, with individual areas of the
male and female in each breeding pair overlapping extensively. After the death
of both individuals of one pair, the neighboring pair progressively occupied
the vacant space, expanding markedly its range into about half the area
originally occupied by the previous pair. Factors driving a pair of Hoary Foxes to expand their territory into a
vacant area after death of the neighboring pair were not clearly determined. Absence of territorial defence, however,
could have contributed to the range shift observed. This is the first
time that the response of neighboring foxes to social disruption of an adjacent
pair has been documented for Hoary Foxes.
Keywords: Cattle pastures, movement patterns, South American Canidae, territoriality.
Portuguese Abstract: Resumo: A raposa-do-campo Lycalopex vetulus, é um pequeno canídeo insetívoro-omnívoro que habita ambientes abertos da savana brasileira, cuja organização espacial e territorialidade ainda é desconhecida. Uso do espaço e organização social de dois casais reprodutivos com áreas domiciliares adjacentes foram determinadas através de rastreamento por rádio telemetriade outubro de 2002 a abrilde 2003 em um mosaico de pastagens e vegetação de Cerrado no leste de Mato Grosso, Brasil.
As áreas de vida tinham 140–299 ha, com áreas individuais de machos e fêmeas de cada par reprodutivo sobrepondo-se extensivamente. Após a morte de ambos os indivíduos de um dos pares, o par vizinho ocupou progressivamente o espaço vago, expandindo marcadamente sua área em cercade 50% da área originalmente ocupada pelo par anterior. Fatores que levaramum par de raposas para expandir seu território em uma área vaga após a morte do par vizinho não foram claramente determinadas. Ausência de defesa territorial, no entanto, pode ter contribuído para a mudança de área observada. Esta é a primeira vez quea resposta de raposas vizinhas à ruptura social de um
par adjacente foi documentada para a raposa-do-campo.
doi: http://doi.org/10.11609/jott.3082.10.6.11703-11709 | ZooBank:urn:lsid:zoobank.org:pub:D5BA9563-9A43-4D8C-BF60-97B9D05B90D9
Editor: Brian L. Cypher, California
State University ,Bakersfield, USA. Date
of publication: 26 May 2018 (online & print)
Manuscript details: Ms # 3082 |
Received 03 October 2016 | Final received 31 October 2017 | Finally accepted 15
April 2018
Citation: Dalponte, J.C., H.S. Lima, S. Klorfine& N.C. da Luz (2018). Home range and spatial organization by
the Hoary Fox Lycalopex vetulus (Mammalia: Carnivora: Canidae): response to social disruption of two
neighboring pairs. Journal of Threatened Taxa 10(6): 11703–11709; http://doi.org/10.11609/jott.3082.10.6.11703-11709
Copyright: © Dalponte et al. 2018. Creative Commons Attribution 4.0 International
License. JoTT allows unrestricted use of this
article in any medium, reproduction and distribution by providing adequate
credit to the authors and the source of publication.
Funding: The Saint Louis Zoo’s Field Research for Conservation
Program funded this study (FRC #01-15).
Competing interests: The authors declare no competing interests.
Author Details: Julio C. Dalponte: Born in Ribeirão Preto, São Paulo state, Brazil, he received his
undergraduate degree in Biology from the Federal University of Mato Grosso in 1989 and a PhD in
Animal Biology from the University of Brasília in 2003. He is currently an
associate professor and teaches Zoology at the Federal University of Mato Grosso, Campus of Sinop, Mato Grosso State. Herson S. Lima: Born in 1963 in Três Lagoas, Mato Grossodo Sul state, Brazil, he received his undergraduate
degree in Biology from the State University of Mato Grosso, Mato Grosso,
Brazil, in 2002. He did a specialization course in savannaecology from this same institution, presenting a course conclusion monograph on
the space use of the Hoary Fox in the Cerrado biome.
He currently works on his cattle ranch and is a consultant in field
biology. Stuart Klorfine: Born in 1970 in
Seattle, WA, US, he holds a degree in Ecology and Ethology from Antioch
University in 1998. Stuart has developed studies on medium and large mammals inagroecosystems and protected areas of Mato Grosso. He currently works
as a biology consultant, with emphasis on conservation and monitoring of wild
mammals. Nelton C. da Luz: Born in Canarana,
Brazil, in 1983. He received the B.S. degree in biology from the State
University of Mato Grosso, Mato Grosso, Brazil, in 2008 and
the M.S. degree in management of natural resources and local development in the
Amazon from the Federal University of Para, Belem, Brazil, in 2011. He is
currently with the Regional Center of the Amazon,
National Institute for Space Research–INPE-CRA, Belem, Brazil.
Author Contribution: JCD: Project Coordinator, fund raising, obtaining field data, data
analysis and preparation of the final version of the manuscript. HSL: Obtaining
field data, data analysis and preparation of first version of the manuscript.
SK: Fund raising, obtaining field data, and data analysis. NCdaL:
Help in field work and data analysis.
Acknowledgements: We thank E.S. Lima for field for
assistance in the field, and E.C. Rocha, W. Tomas, M.R. Pitman, and V. Queirogas by early manuscript revisions.
Introduction
The Hoary Fox Lycalopex vetulus, is a non-cooperative, solitary, small canid (3–4 kg body weight) with a distribution restricted to Brazil (Dalponte 2009). It is classified as a species of Least Concern (Dalponte & Courtenay 2004) for conservation purposes. In a more recent assessment, however, it has been classified as
Vulnerable to extinction in Brazil (Lemos et al. 2013).
The Hoary Fox inhabits open areas of
Brazil, particularly the herbaceous and sub-shrubland of the Cerrado (Brazilian savannah), transitional
areas, and cattle pastures (Dalponte & Courtenay 2004; Rocha et al.
2008). It is an omnivore-insectivore consumer (Dalponte 1997). Although with no morphological
adaptations that enable them to gain access to the concealed termite galleries
of hard exposed above-ground nests, such as those found in true myrmecophagous mammals, it is an active predator of leaf-feeding termites (Dalponte 1995; Dalponte 1997; Juarez & Marinho Filho 2002; Dalponte 2003; Dalponte & Courtenay 2004; Jácomo et al. 2004; Courtenay et al. 2006; Lemos & Facure 2011). Rich
termite patches occur in cattle pastures (mainly above-ground concentrations ofSyntermes and Cornitermes species) along with dung beetles, and these resources are exploited on a
seasonal and opportunistic basis (Ferreira-Silva & Lima 2006).
In central Brazil, the Hoary Fox can
subsist foraging and breeding in cattle pastures
year-round (Juarez & Marinho-Filho 2002; Dalponte 2003; Courtenay et al. 2006). Hoary Fox can reach densities of 1.5
foxes/km² (radio tracking; Courtenay et al. 2006).
The Hoary Fox has a monogamous mating
system consisting of a reproductive pair with
extensively overlapping home ranges (Dalponte 2003; Dalponte & Courtenay 2004; Courtenay et al.
2006). Data on home ranges, spatial
organization and territoriality of the Hoary Fox is scarce, and restricted to
four studies in central Brazil (Juarez & Marinho Filho 2002; Dalponte 2003; Courtenay et al. 2006; Lemos 2016). Field data on the social behavior of the
Hoary Fox, related to temporo-spatial aspects, social interactions and
habitat use are limited by few studies (Dalponte 2003; Courtenay et al. 2006; Lemos 2016). The spatial relationship between
neighboring pairs of Hoary Fox, however, is still unknown, as well as the
factors related to changes in home range size.
Home ranges are relatively confined areas
where most animals carry out their daily activities and
should be defined relative to a specific time interval (Powell 2000). Home ranges of mammalian carnivores may
vary in size depending on body size (Gittleman & Harvey 1982), and tend to be
larger as animal size increases (Ewer 1973). Ranges can also vary according to sex,
habitat type distribution and availability (Ross et al. 2012), and productivity
of the habitats, as well as food dispersion and availability (Macdonald 1983; Sandell 1989). Considering food availability, for example, ranges may be larger where prey density is lower (Zoellick & Smith 1992), and smaller where
food resources are clumped (Eide et al. 2004).
A territory is an area within an animal’s
home range over which the animal has exclusive or priority use, and it may comprise the animal’s entire home range (Powell
2000). Territoriality is an
important mechanism by which social carnivores limit or exclude potential
competitors of the same species from access to mates, food, space, and cover (Mech 1970; Gese 1998).
Owners of territories usually win
territorial disputes against intruders of the same species. Winners in the competition for
territories achieve considerable direct and indirect reproductive benefits (Alcock 2005). A territory should provide all the key resources for an individual or group, allowing
self-sufficiency within the smallest possible area (Vaughan 1978). Neighbors of the same species represent
potential competitors for space, food and partners (Mech 1970; Gese 1998). Territoriality
limits the number of animals competing for food resources, mating opportunities
and formation of new social groups. Territorial behavior in carnivores includes
vocalizations, postures and odoriferous marking at territory boundaries (Brown
& Orians 1970; Kruuk1972; Peters & Mech 1975; Harrington & Mech 1978).
Olfactory communication plays an
important role in the social life of carnivores, especially strongly
territorial species (Ewer 1973; Macdonald 1983; Gorman & Trowbridge
1989). Urine and feces constitute scent marks used by carnivores and have an advantage over
other ways of communicating due to their persistence in the environment, and
because they do not require the territory owner to be physically present (Ewer
1973). Scent marking as a form of territorial definition is well established in larger canids such as the Gray Wolf Canis lupus and Coyote Canis latrans (Allen et al. 1999), but is less well
studied in smaller canids.
Amongcanids, defense of territories is usually
conducted by the dominant pair (Mech 1970; Macdonald 1979; Ralls et al. 2007; Darden et al. 2008;
Arnold et al. 2011). In the event of social disruption, the
absence of these dominant individuals can enable the neighboring pair to
attempt to expand into the non-defended area (Gese 1998).
Studies on territoriality in canids indicate that changes on spatial
distribution between social units may occur due to shifts in territorial
boundaries in response to loss of one or both individuals
of the alpha pair (Gese 1998). Data on usurping a vacant territory due
to death or abandonment by the original occupants are rarely recorded among canid species due to the difficulty of
observing elusive and nocturnal carnivores (Mech 1974; Kleiman & Brady
1978; Gese 1998).
The aims of this study were to describe
the home ranges and document patterns of home range overlap of two neighboring
Hoary Fox mated pairs, and to document for the first time the responses of
neighboring Hoary Fox dyads to removal of an adjacent pair.
Material and Methods
The social organization of Hoary Fox
(Images 1,2) was studied in an area of 6.5km² located at Laranjal Ranch, 10km north of Nova Xavantina (14033’S & 52023’W; Fig. 1), eastern Mato Grosso State, Brazil. The local
landscape consists of patches of Cerrado vegetation in a matrix of cultivated
pasture and field crops. Pastures are permanent and composed of introduced,
exotic African grasses (Brachiaria and Andropogon) that range from 10–80 cm
high. The pastures support high densities of leaf-feeding termites consisting of above
ground mounds of Cornitermes and below ground nests of Syntermes (Ferreira-Silva & Lima 2006; Image
3). Every year from November to
April, a monoculture crop of soybean dominates part of the landscape, and from May to October the ground remains almost totally
exposed, with some grasses and shrubs composing the vegetation. Climate has two distinct seasons: wet
(October–March) and dry (April–September), type Aw in the Köppenclassification (Alvares et
al. 2013). Average yearly rainfall
is around 1,600mm (Nimer1981).
Foxes were captured with leghold traps (coil spring soft-catch foothold
traps Victor 1.1 / 2 x 2; Woodstream Corporation, Lititz, Pennsylvania, USA)
and immobilized with Zoletil 50® (dosage 0.1ml / kg body
weight), measured, weighed, sexed and fitted with very high frequency (VHF)
radio transmitters (Telonics, Inc.) weighing about 3% of the animal
body weight.
Captures followed the procedures recommended by the American Society of Mammalogy (Sikes & Gannon 2011), and the Brazilian Law Nº 11.794, of 08 October, 2008 which regulates procedures for the
scientific use of animals, and were approved by the Brazilian Government (Chico
Mendes Institute Biodiversity Conservation - ICMBio / SISBIO’s
Permanent Collection License # 15524).
Radio
locations were obtained by triangulation from
three fixed towers located on internal roads in the study area, using a
two-element Yagi antenna. Foxes were monitored an average of three
sessions per week, totaling 66 sessions at dawn and dusk
(between 17:00hr and 07:00hr). Triangulations to calculate the location of each individual were made
through Trackmaker 12 program, and size of home ranges were
compared with 100% and 95% of the locations by the minimum
convex polygon (MCP; Mohr 1947). Home range and overlapping areas between pairs were estimated using ArcGIS 9.3 software (ESRI 2010). Additionally, 10 sessions between 08:00hr
and 15:00hr were previously conducted to check daytime activity.
All foxes were located during each
monitoring bout, yielding up to three triangulations per individual, with an
interval of 1.5–2 h between each triangulation.
Two mated Hoary Fox pairs (male M1 and
female F1 of pair P1 and male M2 and female F2 of pair P2)
with adjacent ranges were followed from October 2002 to April 2003. To better understand changes in size and
shape of home ranges of the breeding pairs, we divided the study period into
three distinct phases. The first
phase comprised the first three months of the study (Phase I: 1
October to 31 December 2002), during which the two breeding pairs (P1 and P2)
associated with their offspring and occupied stable areas. The second phase
(Phase II: 5 January to 7 February 2003), started with the death of F2, during which M2 alone took care of the puppies. The third phase (Phase III: 9 February
to 9 April 2003), began after the death of M2. Urine marking behavior was opportunistically
recorded during radio tracking.
Results
A total of 174 radio locations were obtained for male M1, and 169 for
female F1 from 1 October 2002 to 9 April 2003. We obtained 127 radio locations for male M2 from 1 October 2002 to 7
February 2003, and 76 locations for female F2 from 1 October to 31 December
2002.
Pair P2 was monitored
for a shorter period because the female F2 was killed by domestic dogs Canis familiaris on 5 January 2003 and male M2 died with
symptoms of pesticide poisoning on 9 February 2003. Estimated home ranges (MCP 100%) of M1
and F1 were 421ha and 458ha, respectively, and those of M2 and F2
were 401ha and 205ha (Table 1). Estimated ranges of M1 and F1 (95% MCP) were 283ha and 299ha,
respectively, and to M2 and F2 (95% MCP) were 204ha and 140ha, respectively
(Table 1). Home range size did not differ greatly between individuals, but did differ between different phases of the
study (Table 2). The smallest area was that of F2 (140ha) in the first phase,
and the largest was that of F1 (299ha) in the third phase.
In Phase I, the overlapping area between
pairs P1 and P2 was small, ranging from 22ha to
24ha with an estimated average overlap of 13% (Fig. 2 and Table 3). In Phase II, there was an advance of
pair P1 over the area of pair P2, ranging from 30ha to 41ha, and an estimated
average overlap of 22% (Fig. 3 and Table 4). In Phase III the expansion was
substantial, ranging from 68ha to104ha, and an average overlap estimate of 53%
(Fig. 4 and Table 4).
No activity was detected during diurnal
monitoring bouts. Foxes exhibited
activity after dark, but by the first light of day they were already in
their resting sites.
Table 1. Arithmetic mean home ranges
sizes (Minimum convex polygon - MCP 100% 95% and) of four Hoary Foxes Lycalopex vetulus(two breeding pairs) from 01 October 2002 to 09 April 2003, at Nova Xavantina, Mato Grosso State, Brazil.
Fox |
Monitoring period (days) |
Number of locations |
Home range
MCP (ha) 100% 95% |
M1 |
191 |
174 |
421 223 |
F1 |
191 |
169 |
458 240 |
M2 |
130 |
127 |
401 200 |
F2 |
92 |
76 |
205 140 |
M1 - Male Pair 1; F1 - Female Pair 1; M2 - Male Pair 2; F2 - Female
Pair 2
Table 2. Home ranges (Minimum convex polygon
95%) of four Hoary Fox Lycalopex vetulus (two breeding pairs) analyzed in three distinct
phases in Nova Xavantina, Mato Grosso State, Brazil.
Phase |
Fox |
Monitoring period (days) |
Number of locations |
Home range (ha) |
1 |
M1 |
92 |
83 |
170.6 |
1 |
F1 |
92 |
77 |
190.2 |
1 |
M2 |
92 |
82 |
196.7 |
1 |
F2 |
92 |
76 |
140 |
2 |
M1 |
130 |
148 |
214.6 |
2 |
F1 |
130 |
125 |
230.7 |
2 |
M2 |
130 |
127 |
204.2 |
3 |
M1 |
191 |
174 |
283.7 |
3 |
F1 |
191 |
169 |
299.3 |
Table 3. Home range overlap between two Hoary Fox Lycalopex vetulus breeding pairs in the first phase of the study (01 October to 31
December 2002).
Overlap percentages |
||||
Foxes |
M1 |
F1 |
F2 |
M2 |
M1 |
|
141ha - 74% |
23ha - 16% |
23ha - 11% |
F1 |
141ha - 82% |
|
22ha - 15% |
24ha - 12% |
F2 |
23ha - 13% |
22ha - 11% |
|
135ha - 68% |
M2 |
23ha - 13% |
24ha - 12% |
135ha - 96% |
|
Table 4. Home range overlap between
individuals of two Hoary Fox Lycalopex vetulus breeding pairs in the second phase of the study
(05 January to 7 February 2003).
Overlap percentages |
||||
Foxes |
M1 |
F1 |
F2 |
M2 |
M1 |
|
197ha - 85% |
31ha - 22% |
30ha - 15% |
F1 |
197ha - 92% |
|
38ha - 27% |
41ha - 20% |
F2 |
31ha -14% |
38ha -17% |
|
|
M2 |
30ha - 15% |
41ha - 18% |
|
|
Table 5. Home range overlap between individuals of two breeding
pairs of Hoary Foxes Lycalopex vetulus in the third phase of the study (9 February to 9 April 2003).
Overlap percentages |
||||
Foxes |
M1 |
F1 |
F2 |
M2 |
M1 |
|
259ha - 87% |
68ha - 49% |
81ha - 40% |
F1 |
259ha - 92% |
|
92ha - 65% |
104ha - 50% |
F2 |
68ha - 24% |
92ha - 30% |
|
|
M2 |
81ha - 29% |
104ha - 35% |
|
|
Discussion
The largest Hoary Fox home ranges
described in the present study (140–299ha using MCP 95% were smaller than those reported in previous studies
conducted in central Brazil (Juarez & Marinho-Filho 2002; Courtenay et al. 2006; Lemos 2016). Juarez & Marinho-Filho (2002), using the MPC, but without
information on the percentage of the locations used in the calculations,
estimated home ranges of 208 and 385ha for a young and a lactating female Hoary Fox, respectively. Lemos (2016), working in Southern GoiásState with a larger sample of individuals (n = 38), estimated an average adult
Hoary Fox home range area of 268ha, using 95% kernel density autocorrelation
estimator (AKDE) over 392 days.
Courtenay et al. (2006) reported
overlapping among a family group of between 420ha and 456ha respectively, using
the restricted polygon 95% and grid cell 95% in 12 months from August 1991 to July 1993. Different methods in estimating home
range sizes, more extensive tracking periods and more individuals monitored in
previous studies, may contribute to the relatively smaller size of the home
range areas we reported.
An additional factor influencing the
range size of Hoary Fox in our study may be the movement
restriction during the reproductive stage, including the period dedicated to
raise offspring, when mobility of breeding pairs and family groups may be
limited to their natal range (Courtenay et al. 2006).
The Hoary Fox may be able to subsist in cattle pastures
by adopting a primarily insectivorous diet throughout the year, consuming large
proportions of leaf-feedingtermites in the dry season and dung beetles in the rainy
season (Ferreira-Silva
& Lima 2006). Although arthropods, particularly
soldiers and workers of leaf-feedingtermites, have low nutritional values for mammals (Redford
& Dorea 1984), pastures provide relatively
abundant and concentrated resources for Hoary Fox. We hypothesized that these resource
concentrations can meet food demands for Hoary Fox all year round and also
permit the foxes to use relatively small home ranges.
Factors driving a pair of Hoary Foxes to
expand their territory into a vacant area after death of the neighboring pair were not clearly determined. The
Hoary Fox exhibit several potential forms of territorial defence (e.g., urine
marking, scat deposition, body rubbing, scraping and roar barking; Dalponte 2003). The absence of any of these could have contributed to the changes in the
spatial organization.
Although the number of monitored foxes
was small, this is the first time that the responses of neighboring foxes to
social disruption of an adjacent pair have been documented for Hoary Foxes.
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