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1 August 2006 Preliminary Evaluation of the Conservation Status of Callicebus coimbrai in the Brazilian State of Sergipe
Leandro Jerusalinsky, Marcelo M. Oliveira, Ronaldo F. Pereira, Valdineide Santana, Paulo César R. Bastos, Stephen F. Ferrari
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Endemic to the Atlantic forest of the Brazilian states of Sergipe and Bahia, Callicebus coimbrai survives in a highly fragmented landscape characterized by small remnants of forest in a matrix of plantations and pasture. First described only seven years ago, the species is still poorly known and, until the present study, had been recorded from only fifteen sites in Sergipe, in fragments of no less than 40 ha. Here, we report on a survey of the presumed range of the species in Sergipe, with the primary aims of identifying remnant populations and evaluating the influence of factors, such as fragment size, on survival. Populations of C. coimbrai were recorded through either sightings or response to playbacks of vocalizations at 30 of 147 sites surveyed (including 15 confirmed previously), and consistent reports from local residents were obtained at a further 46 localities. Six of the confirmed fragments were less than 20 ha, including one of only 3 ha. This indicates that the species is relatively tolerant of habitat fragmentation, and is able to survive in isolated forests of small size. Together with the growing number of known (and potential) populations, this tolerance is a positive factor for the long-term conservation of the species. However, based on the results of this survey, estimates of the total area of forest occupied by the species, and numbers remaining in the wild are only 100–150 km2 and 500–1,000 individuals, respectively. Clearly, this situation requires urgent measures, including the implementation of protected areas and provisions for metapopulation management.


Coimbra-Filho's titi monkey, Callicebus coimbrai, was first described by Kobayashi and Langguth in 1999, and is considered to be one of the most endangered of all Neotropical primates (Brazil, MMA 2003; IUCN 2004). Its known range covers little more than 30,000 km2, straddling the border between the states of Sergipe and Bahia, an area that has suffered deforestation and habitat fragmentation virtually since the beginning of European colonization, five centuries ago (Coimbra-Filho and Câmara 1996).

By the beginning of the 20th century, the Atlantic forest of Sergipe had been reduced to approximately 40% of its original cover, and to less than 1% over the subsequent 100 years (Siqueira and Ribeiro 2001). This remnant forest cover is distributed in isolated fragments of no more than 900 ha. Prior to the present study, C. coimbrai had been recorded from 15 sites in Sergipe, and two in Bahia (Kobayashi and Langguth 1999; Sousa 2000, 2003; Printes 2005), in forest fragments ranging in size from 40 to 900 ha. It is not known to occur in any officially protected areas in either state (Silva et al. 2005).

In the present study, the known and presumed distribution of C. coimbrai in the state of Sergipe was surveyed systematically in an attempt to locate additional remnant populations and define ecological parameters such as the minimum size of fragment necessary for the survival of the species. The data collected were used for an overall assessment of the conservation status of the species in this state, and the formulation of basic guidelines for the development of long-term conservation strategies.


Fieldwork was planned on the basis of known C. coimbrai localities in Sergipe (Kobayashi and Langguth 1999; Sousa 2000, 2003) and the identification of potential sites using a digital atlas of the state (Sergipe, SEPLANTEC 2004) using satellite images and aerial photographs. The primary strategy was to survey all fragments of large size (>100 ha), and to sample smaller fragments within the survey area; in particular those for which local residents had indicated the presence of C. coimbrai.

Four main study areas were demarcated (Fig. 1) and surveyed during separate excursions between May and September 2004. In November 2004, and March and May 2005, complementary excursions were conducted to survey previously visited localities where the species had been indicated consistently in interviews, but not confirmed directly. During visits to each site, experienced local residents were interviewed in a standardized, undirected manner, supported by photographs and drawings of local mammals, and by recordings of Callicebus vocalizations, in an attempt to identify local habitat in which titis could be found. Sites indicated consistently by residents were visited and surveyed qualitatively, using existing trails. In addition to observations, recordings of Callicebus vocalizations were played through a loudspeaker (Johnny Stewart 612 Deluxe professional caller) in an attempt to provoke a response from animals out of sight.

Figure 1.

Map of the Brazilian state of Sergipe, showing the four main study areas.


The size of forest remnants was estimated through a combination of the available information (aerial photographs and satellite images) and direct observation. At sites where the presence of C. coimbrai was confirmed, the landowner or property manager was also contacted to obtain more detailed information and to refine estimates. Estimates were less systematic at unconfirmed sites, and given their heterogeneity, they have been assigned to size classes for the purposes of the present study.


A total of 147 forest fragments were identified either during planning, or during surveys, when indicated by local residents. All were visited during the four preliminary excursions, and 28 of them were revisited during the three complementary field trips. In many cases, fragments identified on the digital atlas either no longer existed or had been practically eliminated by deforestation or fire.

Overall, 245 residents were interviewed, and a total of 110 sites were indicated as having resident titis in at least one interview. However, the reports referring to 34 of these sites were considered unreliable because of inconsistencies in the identification of the species. Some interviewees confused titis with capuchins (Cebus) or marmosets (Callithrix), or even other arboreal mammals. The remaining 76 sites included the 15 recorded by Kobayashi and Langguth (1999) and Sousa (2003), and an additional 15 at which the presence of the species was confirmed through either direct observation or response to playbacks (Table 1, Fig. 2). Playbacks proved to be an important survey tool, providing confirmation of the presence of titi monkeys at the majority (63.3%) of the sites.

Table 1.

Confirmed localities for Callicebus coimbrai in the state of Sergipe, Brazil.


Figure 2.

Sites in the state of Sergipe where the presence of Callicebus coimbrai has been confirmed. Sites are numbered as in Table 1.


At the remaining 46 sites (Table 2, Fig. 3), the presence of C. coimbrai was indicated consistently in interviews, but was not confirmed directly through surveys. Many of these fragments were relatively small in size, although records from Fazenda Tuim and Fazenda Sabão (Table 1) do indicate that the species is able to survive in fragments of less than 10 ha. As such, it would seem reasonable to assume that titis are present in many, if not all, of these unconfirmed fragments.

Table 2.

Localities at which the presence of C. coimbrai was reported consistently by local residents, but not confirmed via direct observation.


Figure 3.

Sites in the state of Sergipe where the presence of Callicebus coimbrai was reported by local residents during the present study, but not confirmed directly (see text and Table 2).


The sum of the area of forest at the 30 confirmed sites (Table 1) is just over 5,000 ha, and that of the unconfirmed sites is between 1,500 and 3,500 ha. The results indicate that C. coimbrai is relatively more abundant in the southern coastal forest zone in comparison with the central and northern coastal zones. More than a half of confirmed (55.9%) and unconfirmed (60.9%) sites are located in the basins of the Rios Piauí and Real (Figs. 2 and 3). This area is characterized by seasonal semi-deciduous forest (Brazil, IBGE 2004).

An additional, unexpected result of the surveys was the recovery of an adult female C. coimbrai (Fig. 4) from illegal captivity at Riacho Fundo do Abaís (11°12′ S, 37°20′ W) on 16 March 2005. The animal was taken to the Aracaju Zoological Gardens on the same day, where it was found to be in good health, and has now survived for almost a year. This is the first time the species has been held officially in captivity, and represents a potentially important first step in the eventual development of programs of captive breeding, translocation, and reintroduction.

Figure 4.

Adult female Callicebus coimbrai, resident at the Aracaju Zoological Gardens since 16 March 2005. Photograph by Leandro Jerusalinsky.


A second animal was observed (M. C. Sousa pers. comm.) in private captivity in the town of Nossa Senhora da Glória (Fig. 3), although it escaped before being transferred to Aracaju. This, together with surrounding localities (8, 30, and B in Fig. 2), confirms that, while C. coimbrai is rare in caatinga habitats, where it is replaced by Callicebus barbarabrownae, its original geographic range extends farther north and west than was previously supposed.


In common with most of the platyrrhine species discovered in the wild over the past 15 years (for example, Lorini and Persson 1990; Van Roosmalen et al. 2002), C. coimbrai has a relatively restricted geographic range, which, like most of the Atlantic forest, is characterized by critical levels of deforestation and habitat fragmentation. There was thus little doubt that the species was at some risk of extinction as soon as it was made known to science, and it is now considered to be one of the most endangered of Brazilian primates (Brazil, MMA 2003; IUCN 2004). This study has done little to alter this initial impression, although the species is now known to occur at many more sites than the three localities identified originally by Kobayashi and Langguth (1999). In addition to the thirty sites confirmed here, R. C. Printes (pers. comm.) has recorded C. coimbrai at two additional sites in Sergipe (Fig. 2), bringing the current total to thirty-two. It is important to note that one of the sites reported by Printes is located outside the area surveyed in the present study, suggesting that a certain number of potential sites have yet to be identified.

These sites encompass a total area of approximately 50 km2 of forest. While this is almost certainly an underestimate of the total area of forest in Sergipe occupied by populations of C. coimbrai, it seems unlikely that the definitive value will surpass 75 km2. If it is assumed that a similar situation exists in Bahia, given that the species may be distributed over a similar area in this state (Printes 2005), we can conclude that the total area of forest occupied by the species is between 100 and 150 km2.

Demographic parameters of C. coimbrai populations are not known, and few reliable data are available for the genus. The values most relevant to the present study are those of Müller (1996a) and Heiduck (2002), who recorded home ranges of 22–24 ha for two Callicebus melanochir groups in the Atlantic forest of southern Bahia. Palacios et al. (1997) reported a similar value for the Amazonian Callicebus torquatus. Price and Piedade (2001) recorded smaller home ranges in a shortterm study of Callicebus personatus, although surveys at a number of other sites in southeastern Brazil (Chiarello 2003; São Bernardo and Galetti 2004) returned relatively low population densities for this species, indicative of relatively large home ranges.

Titi monkeys are strictly monogamous and live in small family groups, with three to five members. Callicebus coimbrai appears to be typical in this sense (Sousa 2003; R. C. Printes pers. comm.; this study), and a similar pattern has been reported for the closely related C. melanochir (Müller 1996a; Heiduck 2002), so it would seem reasonable to use four individuals as an approximate mean group size. Using a generous estimate of five groups/km2, the 30 confirmed sites in Sergipe would contain a theoretical total population of approximately 1,000 individuals. Even if this were a gross overestimate, it would still seem reasonable to assume that the number of C. coimbrai surviving in the wild (including both Sergipe and Bahia) may be between 500 and 1,000 individuals.

While this provides some room for cautious optimism, the question of habitat fragmentation cannot be overlooked. Demographic patterns in fragmented habitat are clearly different from those in continuous forest, although the effects are not always negative, depending on the species. One positive aspect of the present study, for example, was the confirmation of the ability of C. coimbrai to survive in forest fragments smaller than 10 ha. Given this, the number of fragments with titis may be as important as the total area of forest for the planning of conservation strategies. The large number of unconfirmed reports (Table 2) certainly suggests that many more small, isolated populations have yet to be discovered.

However tolerant of habitat disturbance C. coimbrai may be, the distribution of remnant populations in a large number of isolated fragments clearly presents a deep-seated problem for long-term management (Vieira et al. 2003). Titi monkeys present an additional unique behavioral problem, among Atlantic forest primates: While the exact mechanism is still unclear (Müller 1996b; Mayeaux et al. 2002), offspring invariably emigrate from their natal groups as they approach sexual maturity, limiting group composition to the breeding pair and their immature offspring.

While this may be an important dispersal mechanism in populations inhabiting continuous forest, it may have deleterious consequences in small fragments, where emigration to a new forest may be the only option for maturing offspring (see Fig. 5). Individuals migrating between fragments over open ground risk predation and exhaustion (mean day range of Atlantic forest titis is approximately 1 km: Müller 1996a; Price and Piedade 2001), with only a very random possibility of encountering a potential reproductive partner. This suggests an extremely inefficient process characterized by high mortality and the frequent loss of reproductive opportunities (for example, animal dispersing to vacant fragments).

Figure 5.

Hypothetical scenario faced by a maturing titi monkey (red animal in fragment A) in the fragmented landscape of the Atlantic forest of Sergipe. Fragment D offers the best opportunities for survival and the establishment of a breeding group, but is farthest from A. Smaller fragments (B and C) are more common, and generally more accessible, but will normally be either at carrying capacity (B) or vacant (C). In either case, the chance to breed will depend on unpredictable, random events such as the disappearance of the same sex adult (B) or the immigration of an adult of the opposite sex (C).


This implies, in turn, that active management of the metapopulation, including both translocation and reintroduction, may be relatively more important for the long-term conservation of C. coimbrai (and other titi species) than for other Atlantic forest primates. The effective implementation of such management will also depend on the establishment of an integrated system of public and privately owned reserves. One important first step in this process is the creation of a federal conservation unit — with the specific aim of protecting C. coimbrai — which is currently being planned by the Brazilian environment institute (IBAMA), based on the results of the present study.


This study was made possible by the helpful cooperation of local residents and landowners throughout the region. We are grateful to Márcio Macedo, Gláucia Bispo and Marleno Costa (IBAMA/SE) for local technical support, to Rodrigo Cambará Printes and Marcelo C. Sousa for unpublished data, and to Paulo José de Oliveira (SEPLANTEC) for providing the digital atlas and aerial photographs. Special thanks to Aline Lima for Figures 1, 2, and 3.

Literature Cited


Brazil, IBGE 2004. Mapa de Vegetação do Brasil. Instituto Brasileiro de Geografia e Estatística. Brasília, Brazil. Website: <>. Accessed 5 August 2005. Google Scholar


Brazil, MMA 2003. Instrução Normativa N° 03, de 27 de maio de 2003: Lista Oficial das Espécies da Fauna Brasileira Ameaçadas de Extinção. Ministério do Meio Ambiente (MMA), Brasília. Diário Oficial da União – Seção 1 101:88–97. Google Scholar


A. G. Chiarello 2003. Primates of the Brazilian Atlantic Forest: The influence of forest fragmentation on survival. In Primates in Fragments: Ecology and Conservation. L. K. Marsh , editor. (ed.), pp. 99–121.Plenum Press. New York. Google Scholar


A. F. Coimbra-Filho and Ide G. Câmara . 1996. Os Limites Originais do Bioma Mata Atlântica na Região Nordeste do Brasil. Fundação Brasileira para a Conservação da Natureza. Rio de Janeiro. Google Scholar


S. Heiduck 2002. The use of disturbed and undisturbed forest by masked titi monkeys Callicebus personatus melanochir is proportional to food availability. Oryx 36:133–139. Google Scholar


IUCN 2004. 2004 IUCN Red List of Threatened Species. IUCN — The World Conservation Union. Gland, Switzerland. Website: <>. Accessed July 2005. Google Scholar


S. Kobayashi and A. Langguth . 1999. A new species of titi monkey, Callicebus Thomas, from north-eastern Brazil (Primates, Cebidae). Rev. Bras. Zool 16:531–551. Google Scholar


M. L. Lorini and V. G. Persson . 1990. Nova espécie de Leontopithecus Lesson, 1840, do sul do Brasil (Primates, Callitrichidae). Bol. Mus. Nac., Rio de Janeiro 338:1–14. Google Scholar


D. J. Mayeaux, W. A. Mason, and S. P. Mendoza . 2002. Developmental changes in responsiveness to parents and unfamiliar adults in a monogamous monkey (Callicebus moloch). Am. J. Primatol 58:71–89. Google Scholar


K-H. Müller 1996a. Diet and feeding ecology of masked titis (Callicebus personatus). In Adaptive Radiations of Neotropical Primates. M. A. Norconk, A. L. Rosenberger, and P. A. Garber , editors. (eds.), pp. 383–401.Plenum Press. New York. Google Scholar


K-H. Müller 1996b. Emigration of a masked titi monkey (Callicebus personatus) from an established group, and the establishment of a new group. Neotrop. Primates 4:19–21. Google Scholar


E. Palacios, A. Rodríguez, and T. R. Defler . 1997. Diet of a group of Callicebus torquatus lugens (Humboldt, 1812) during the annual resource bottleneck in Amazonian Colombia. Int. J. Primatol 18:503–522. Google Scholar


E. C. Price and H. M. Piedade . 2001. Ranging behavior and intraspecific relationships of masked titi monkeys (Callicebus personatus personatus). Am. J. Primatol 53:87–92. Google Scholar


R. C. Printes 2005. Novos registros sobre a distribuição do guigó da caatinga Callicebus barbarabrownae (Hersh kovitz, 1990) e novo limite sul de Callicebus coimbrai (Kobayashi & Langguth, 1999). In. Programa e Livro de Resumos: XI Congresso Brasileiro de Primatologia. p. 154. Porto Alegre, 13–18 de fevereiro de 2005. Sociedade Brasileira de Primatologia. Porto Alegre. (Abstract). Google Scholar


C. S. São Bernardo and M. Galetti . 2004. Densidade e tamanho populacional de primatas em um fragmento florestal no sudeste do Brasil. Rev. Bras. Zool 21:827–832. Google Scholar


Sergipe, SEPLANTEC 2004. Atlas Digital sobre Recursos Hídricos de Sergipe. CD-ROM. Secretaria de Estado do Planejamento e da Ciência e Tecnologia (SEPLANTEC). Aracaju, Sergipe. Google Scholar


T. C F. Silva, L. Jerusalinsky, and M. M. Oliveira . 2005. Primatas endêmicos do Brasil em Unidades de Conservação de Proteção Integral: Registros de ocorrência e taxa desprotegidos. In. Programa e Livro de Resumos: XI Congresso Brasileiro de Primatologia. p. 165. Porto Alegre, 13–18 de fevereiro de 2005. Sociedade Brasileira de Primatologia. Porto Alegre. (Abstract). Google Scholar


E. R. Siqueira and F. E. Ribeiro . 2001. A Mata Atlântica de Sergipe. Embrapa Tabuleiros Costeiros. Aracaju. Google Scholar


M. C. Sousa 2000. New localities for Coimbra-Filho's titi monkey, Callicebus coimbrai, in north-east Brazil. Neotrop. Primates 8:151. Google Scholar


M. C. Sousa 2003. Distribuição do guigó (Callicebus coimbrai) no Estado de Sergipe. Neotrop. Primates 11:89–91. Google Scholar


M. G M. Van Roosmalen, T. van Roosmalen, and R. A. Mittermeier . 2002. A taxonomic review of the titi monkeys, genus Callicebus Thomas, 1903, with the description of two new species, Callicebus berhardi and Callicebus stephennashi, from Brazilian Amazonia. Neotrop. Primates 10:Suppl1–52. Google Scholar


M. V. Vieira, et al 2003. Mamíferos. In Fragmentação de Ecossistemas: causas, efeitos sobre a biodiversidade e recomendações de políticas públicas. D. M. Rambaldi and D. A S. Oliveira , editors. (eds.), pp. 126–151.Ministério do Meio Ambiente (MMA). Brasília. Google Scholar
Leandro Jerusalinsky, Marcelo M. Oliveira, Ronaldo F. Pereira, Valdineide Santana, Paulo César R. Bastos, and Stephen F. Ferrari "Preliminary Evaluation of the Conservation Status of Callicebus coimbrai in the Brazilian State of Sergipe," Primate Conservation 2006(21), 25-32, (1 August 2006).
Received: 1 September 2005; Published: 1 August 2006
Callicebus coimbrai
Coimbra-Filho's titi monkey
Northeast Brazil
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