Mammal survey on the Rio Jauaperí, Rio Negro
Basin,
the Amazon, Brazil
by M. TROLLE
Zoological Museum University of
Copenhagen, Mammal Department,
Universitetsparken 15, 2100 Copenhagen,
Denmark
e-mail: mtrolle@zmuc.ku.dk
Summary. – The Brazilian part of the Rio Negro Basin, a
major region of the Amazon, is one of the least studied regions of the Amazon
rainforest. An intensive, four months inventory of the medium to large,
non-volant mammal species was conducted in the area encompassing the lower Rio
Xixuaú, a minor tributary to the Rio Jauaperí river, to the north
of Rio Negro. The main habitats of the study area were seasonally flooded
igapó forest, riparian vegetation, higher-lying terra firme
forest, secondary forest, minor water courses and lakes. Using walked transects,
camera trapping, observations from canoe, nightspotting, interviews, and
identification of skulls, it was possible to list 43 species for the study site,
including 8 xenarthrans, 7 primates, 12 carnivores and 5 ungulates. The habitat
use of the primate species is analyzed.
KEY WORDS : Mammal
inventory, camera trapping, primate habitat use, Rio Negro region, the Amazon,
Brazil.
INTRODUCTION
The majority of the mammal surveys of the Brazilian Amazon has been
carried out to the south of Rio Amazonas and on tributaries to Rio
Solimões (Voss and Emmons 1996; Patton et al. 2000) – mainly
on white water rivers. The black water Rio Negro Basin is one of
the least studied regions of the Amazon rainforest. The first collections on the
Rio Negro were conducted by the expedition of A. Rodrigues Ferreira in the end
of the eighteenth century, and later, in the nineteenth century, also A.R.
Wallace visited the region. Avila Pires (1964) published a paper on mammals
collected on the Rio Negro close to Manaus. The only recent intensive mammal
inventory of a delimited study site in the Brazilian part of the Rio Negro
region was carried out in the Parque Nacional do Jaú, situated at Rio
Jaú, to the south of Rio Negro (M.N.F. da Silva, personal communication)
- a study that focused on small mammal trapping (Patton and da Silva,
unpublished species list). Rio Jauaperí, where this study took place,
runs to the north of Rio Negro, which is a major distribution barrier for many
mammal species (Emmons and Feer 1997; Eisenberg and Redford 1999).
An
intensive, four months mammal inventory was conducted in the Xixuaú
Nature Reserve, situated on the western side of the middle Rio Jauaperí,
Roraima state, Brazil (headquarters at S 0º48.023’, W
61º33.476’). Xixuaú Nature Reserve is an area of approximately
150,000 ha of mostly pristine rainforest. The study area consists of the typical
forest habitat types of the region; higher-lying unflooded terra firme
forest, lower-lying seasonally flooded igapó forest and riparian
vegetation, as well as secondary forest at various successional stages, a few
minor plantations, minor water courses and lakes. During the floodseason the
area receives ‘black’ water from Rio Jauaperí, and the
igapó is flooded by black water, however, a couple of months a year,
during the low water season, the water courses inside the Nature Reserve are
exceptionally clear and the water less acidic. The study focused on the area
encompassing the lower Rio Xixuaú, a narrow river in the southern part of
the Nature Reserve.
The study was conducted starting at the peak of the low
water season of the beginning of 2001 when all of the igapó forest was
dry. During the study period, the rainy season began and waters rose
considerably, and at the end of the study period the igapó was starting
to flood. Observations from an earlier one-month visit to Xixuaú in
August 1996, at the peak of the flood season, are included.
The area was
traditionally inhabitated by indigenous people, who must have carried out
subsistance hunting. For more than three decades, the area has been inhabited by
only a few caboclo families and, besides poaching of cats and otters,
hunting pressure was probably light. Hunting ceased altogether with the
establishment of the Xixuaú Nature Reserve about 10 years ago.
The
main aim of this study was to inventory the medium to large, non-volant mammal
species of the area. In addition, the habitat use of primates in the area was
studied in more detail.
MATERIALS AND METHODS
The following methods were used: camera trapping, diurnal and nocturnal
walked transects, diurnal and nocturnal observations from canoe, identification
of tracks, interviews of knowledgeable reserve staff, and, in the case of one
species, identification of skull and skeletal parts.
Six TrailMaster camera
traps with infrared trigger mechanism were used (TM 550 Passive Infrared Trail
Monitor + TM35-1 Camera Kit) (Goodson and Associates, USA). Trap stations were
often baited (Table 2).
A system of nine transects was established and used
for the daily surveys. The trails were situated along an 8 km stretch of the
lower Rio Xixuaú and its tributaries. The trail system covered all of the
above mentioned major terrestrial habitat types. On the walked transects,
observations of animals heard close to the trail were included (typically
flushed animals and monkeys). Animal signs that could be identified to species
level, such as armadillo burrows and tapir droppings, were also recorded.
For
the interviews I relied mostly on two very knowledgeable locals: Carlos Roberto
Nascimento who has lived for 25 years in Xixuaú, and worked for many
years as a poacher of wild cats and Giant Otters, and João Soares Gomes
da Silva, who has spent his entire life working inside the forest, and has lived
about 10 years in Xixuaú. Both men have worked extensively as guides in
the reserve.
TABLE 1. - List of mammals of the lower Rio Xixuaú
area.
Abbreviations. Survey methods:
A=acoustic record; B=burrows; C=camera trapping; I=interviews; Sk=skull;
V=visual record; T=tracks (footprints, scats). Assessment of relative
abundance: c=common; s=significant seasonal variation in local abundance.
DIDELPHIMORPHIA
|
|
|
|
Didelphidae
|
Didelphis marsupialis
|
Black-eared Opossum
|
CV-c
|
XENARTHRA
|
|
|
|
Myrmecophagidae
|
Cyclopes didactylus
|
Pygmy Anteater
|
I
|
|
Myrmecophaga tridactyla
|
Giant Anteater
|
C
|
|
Tamandua tetradactyla
|
Southern Tamandua
|
V-c
|
Bradypodidae
|
Bradypus tridactylus
|
Pale-throated Three-toed Sloth
|
V
|
Megalonychidae
|
Choloepus didactylus
|
Amazon Two-toed Sloth
|
Sk
|
Dasypodidae
|
Dasypus kappleri
|
Great Long-nosed Armadillo
|
CB-c
|
|
Dasypus novemcinctus
|
Nine-banded Armadillo
|
VB-c
|
|
Priodontes maximus
|
Giant Armadillo
|
CB-c
|
PRIMATES
|
|
|
|
Callitrichidae
|
Saguinus midas
|
Golden-handed Tamarin
|
VA-c
|
Cebidae
|
Alouatta seniculus
|
Red Howler Monkey
|
VA-c
|
|
Ateles paniscus
|
Red-faced Black Spider Monkey
|
VA-c
|
|
Cebus apella
|
Tufted Capuchin
|
VA-c
|
|
Chiropotes satanas
|
Brown Bearded Saki
|
VA-c
|
|
Pithecia pithecia
|
White-faced Saki
|
VA-c
|
|
Saimiri sciureus
|
Amazon Squirrel Monkey
|
VA-c
|
CARNIVORA
|
|
|
|
Canidae
|
Speothos venaticus
|
Bush Dog
|
I
|
Procyonidae
|
Nasua nasua
|
Ring-tailed Coati
|
I
|
|
Potos flavus
|
Kinkajou
|
I
|
Mustelidae
|
Eira barbara
|
Tayra
|
CV-c
|
|
Galictis vittata
|
Grison
|
I
|
|
Lontra longicaudus
|
Neotropical River Otter
|
I
|
|
Pteronura brasiliensis
|
Giant Otter
|
VBA-cs
|
Felidae
|
Leopardus pardalis
|
Ocelot
|
I
|
|
Leopardus wiedii
|
Margay
|
I
|
|
Herpailurus yaguarondi
|
Jaguarundi
|
I
|
|
Panthera onca
|
Jaguar
|
V
|
|
Puma concolor
|
Puma
|
C
|
CETACEA
|
|
|
|
Platanistidae
|
Inia geoffrensis
|
Boto River Dolphin
|
V-cs
|
Delphinidae
|
Sotalia fluviatilis
|
Tucuxi Dolphin
|
V
|
PERISSODACTYLA
|
|
|
|
Tapiridae
|
Tapirus terrestris
|
Brazilian Tapir
|
CT-c
|
ARTIODACTYLA
|
|
|
|
Tayassuidae
|
Pecari tajacu
|
Collared Peccary
|
CV-c
|
|
Tayassu pecari
|
White-lipped Peccary
|
I
|
Cervidae
|
Mazama americana
|
Red Brocket
|
CV-c
|
|
Mazama gouazoupira
|
Brown Brocket
|
I
|
SIRENIA
|
|
|
|
Trichechidae
|
Trichechis inunguis
|
Amazonian Manatee
|
V-s
|
RODENTIA
|
|
|
|
Sciuridae
|
Sciurus cf. aestuans
|
Brazilian Brown Squirrel
|
V
|
Erethizontidae
|
Coendou prehensilis
|
Brazilian Tree Porcupine
|
I
|
Hydrochaeridae
|
Hydrochaeris hydrochaeris
|
Capybara
|
I-rare
|
Agoutidae
|
Agouti paca
|
Paca
|
CV-c
|
Dasyproctidae
|
Dasyprocta agouti
|
Red-rumped Agouti
|
CVA-c
|
|
Myoprocta acouchy
|
Red Dwarf Agouti (Acouchy)
|
CVA-c
|
Echimyidae
|
Proechimys sp.*
|
Spiny Rat
|
C
|
* Identified by J.A. de Oliveira and L.M. Pessôa from
camera trap photo
Note: the scientific names generally
follow Wilson and Reeder (1993).
TABLE 2. - Camera trapping
results.
Abbreviations. Site of camera trap: fish bait =
fish bait covered by leaves; veg bait = vegetarian bait (banana, manioc, food
left overs, salt); nat trail = natural trail; hum trail = human trail; mud = mud
wallow/watering hole ; trunk = hollow
trunk.
Species
|
No of photos
|
Sites
|
Didelphis marsupialis
|
175
|
Fish bait 150; veg bait 18; hum trail 6; mud
1
|
Myrmecophaga tridactyla
|
3
|
Fish bait/scratching tree 2, mud/salt 1
|
Dasypus kappleri
|
3
|
Cavity in trunk/nat trail 3
|
Dasypus*
|
15
|
Mud 9; hum trail 2; nat trail 4
|
Priodontes maximus
|
13
|
Burrow 6; dug up termite nest 7
|
Eira barbara
|
1
|
Veg bait
|
Puma concolor
|
1
|
Hum trail/fish bait/scratching tree
|
Tapirus terrestris
|
11
|
Nat trail 1; veg bait 1; salt 4; mud 5
|
Pecari tajacu
|
43
|
Fish bait 7; mud 4; water 11; bed 21
|
Mazama americana
|
6
|
Hum trail 3; salt 2; bed of peccaries 1
|
Agouti paca
|
6
|
Veg bait 1; hum trail 3, mud 1; trunk 1
|
Dasyprocta agouti
|
14
|
Nat trail 1; veg bait 3, salt 2; mud 4; trunk
4
|
Myoprocta acouchy
|
1
|
Mud
|
* Photos where it was not possible to distinguish between
D. kappleri and D. novemcinctus
RESULTS
More than 750 records of mammals were obtained by sightings, acoustic
records and camera trapping. The inventory includes 43 species (Table 1), out of
which 23 were sighted, 13 were recorded by camera trapping, and an additional 13
‘reliable’ species were reported by the locals of Xixuaú. The
study design did not allow for precise estimates of abundance of the species,
however, several of the species were recorded frequently enough to conclude that
they were common. This information is included in Table 1.
Table 2 lists the
results of the camera trapping, giving information on the sites and bait types
used successfully to record the various species.
Primate
observations
The only monkeys observed frequently in the
igapó forest during the survey were Howlers and Capuchins. During the low
water season the diverse and abundant primate fauna is found in the terra firme.
In order to analyze the habitat use of the primates in the terra firme
forest, four of the most walked transects were chosen, representing a grade from
very tall, open, undisturbed primary forest to forest with many tree falls and
much natural secondary vegetation. The average time it took to walk a transect
was about the same on these four trails, so the results are comparable. Two
measures were calculated: a sighting index (i.e. the frequency of recording a
species per walked transect), and the number of records of a species on a trail
divided by the total number of primate records on that trail (i.e. how
frequently a species was observed on a trail in comparison to the other species)
(Table 3).
All seven species of primates were observed carrying young
throughout the study period.
Squirrel Monkeys and Capuchins are known to
commonly associate (Emmons and Feer 1997). During our study, we saw 22 examples
of such mixed troops. The only other species often seen associating was the
Bearded Saki. We had several observations of a single Bearded Saki moving
together with either Spider Monkeys (n=3) or mixed Capuchin/Squirrel Monkey
troops (n=3).
TABLE 3. - Occurrence of primates in
various types of terra firme forest.
Data from four terra firme trails grading from very tall
and open to relatively disturbed forest. Sighting index = no. of obs. of sp. /
no. of transects walked; % = no. of obs. of sp. / total no. of primate obs. on
trail (see text for explanation).
Trail habitat
|
Very tall, open, many thick trees, little
secondary vegetation
|
Tall, relatively open, relatively little
secondary vegetation
|
Part of trail tall, relatively open forest,
other part of trail with much secondary vegetation
|
Diverse mixture of tall primary and many
patches of secondary vegetation around tree falls
|
No. of transects walked
|
10
|
15
|
27
|
15
|
Total no. of primate obs.
|
26
|
37
|
90
|
34
|
|
Index
|
%
|
Index
|
%
|
Index
|
%
|
Index
|
%
|
S. midas
|
.9
|
34
|
.2
|
8
|
.5
|
16
|
.75
|
32
|
A. seniculus
|
.7
|
37
|
.6
|
24
|
.55
|
17
|
.45
|
21
|
A. paniscus
|
.8
|
31
|
.85
|
35
|
.4
|
12
|
0
|
0
|
C. apella
|
.1
|
4
|
.4
|
16
|
.85
|
26
|
.6
|
26
|
C. satanas
|
.1
|
4
|
.15
|
5
|
.2
|
7
|
.15
|
6
|
P. pithecia
|
0
|
0
|
.05
|
3
|
.05
|
1
|
.05
|
3
|
S. sciureus
|
0
|
0
|
.2
|
8
|
.75
|
22
|
.25
|
12
|
DISCUSSION
When opossums (Didelphidae), spiny rats (Echimyidae), and rats and mice
(Sigmodontinae) are excluded, the long-term study at the MSCE Reserves north of
Manaus recorded 32 species of non-volant mammals (Voss and Emmons 1996). In our
study, we found 41 species within this category. The high number compared to the
MSCE reserves is mainly explained by the fact that this area consists
exclusively of terra firme growth, with no major rivers and associated riparian
vegetation.
An additional armadillo species distributed throughout the
Amazon, Cabassous unicinctus, could be expected in the Rio
Jauaperí region. The species is extremely difficult to record in
rainforest; neither L.H. Emmons or J.R. Malcolm, some of the most experienced
field workers in the region, found the species during their extensive studies at
the MSCE Reserves (Voss and Emmons 1996), and only later has it been recorded in
the region by camera trapping (Rittl 1998; Yabe et al. 1998). A second
species of tree porcupine, Coendou melanurus, could also occur (Emmons
and Feer 1997; Eisenberg and Redford 1999), however, the species was not
recorded in the MSCE Reserves, and was not known by locals in Xixuaú.
Habitat use and seasonal local migration of
primates
The data in Table 3 should obviously be viewed with caution, but
nevertheless give a good indication of various trends. Using these results along
with the rest of our observations, in Table 4 I have given a summary of the
overall habitat use of the primate community. The following forest strata
classifications for the terra firme were used: A stratum = tall emergents; B
stratum = the continuous canopy; C stratum = smaller trees (and palms) below the
canopy.
TABLE 4. - Resume of primate habitat use
in Xixuaú.
Species
|
Habitat use
|
Saguinus midas
|
According to Emmons and Feer (1997), unlike other
callithrichids this species tends to frequent open, high forest formations. This
concurs with the observations from Xixuaú. Quite common in both tall,
open mature terra firme forest and terra firme forest with many patches of
natural secondary vegetation. In tall forest they seem to favour trees with
relatively dense foliage. The most commonly observed species in secondary
forest. Strata B-C.
|
Alouatta seniculus
|
Seems to be the most evenly distributed primate species in
the various terra firme forest types, being common in all parts of the terra
firme. Rarely seen in secondary forest, but relatively common in igapó
forest, both during the low water and the flood season. Strata
A-B.
|
Ateles paniscus
|
Seems to be the most specialized primate habitat wise;
almost exclusively recorded in tall, open mature forest with relatively little
disturbance, and were never recorded in secondary forest or igapó. In
their prefered habitat they may be the most commonly recorded monkey. Strata
A-B.
|
Cebus apella
|
The most recorded of all the primates, partly due to its
relative abundance in the igapó, where, during the low water season, it
is the most abundant species. Relatively uncommon in tall, open mature terra
firme forest, but very common in the more heterogenous terra firme with tree
falls, and also relatively common in disturbed forest. When in mixed groups with
Squirrel Monkeys, they are on average higher up in the forest. Strata
B-C.
|
Chiropotes satanas
|
The least commonly observed monkey, and half of the
observations were of single individuals. This may be partly explained by the
fact that troops use large areas of several square kilometers (Emmons and Feer
1997), and, next to Squirrel Monkeys, this was the species seen in the largest
groups. One troop of at least 45 individuals was encountered. They were found in
the whole range of terra firme forest types. Never recorded in secondary forest,
but, observed in igapó during the flood season. Strata
B-C.
|
Pithecia pithecia
|
Another less commonly recorded species, which may be partly
due to its generally shy, silent and secretive behavior. Rarely observed deep in
the mature terra firme forest, and prefers secondary forest and edge habitats
(e.g. between igapó/terra firme and secondary/primary forest). During the
flood season, the species enters the igapó. Strata B-C.
|
Saimiri sciureus
|
Uncommon in tall, undisturbed terra firme forest, and
favoured terra firme forest with a high degree of natural disturbance to an even
greater extent than the Tufted Capuchin, with which it often associates. Often
seen in palms. This is a common species in secondary forest and was also
observed frequently in riparian vegetation at the edge of rivers and clearings,
both during the low water and flood season. Strata C.
|
During the dry season when fruit is scarce inside the
seasonally flooded igapó the only common monkeys found in this part of
the forest are Howlers (specialized folivores) and Capuchins (omnivores) (Emmons
and Feer 1997), both able to get by without fruit. During my flood season visit
in 1996 I recorded also White-faced Saki, Brown Bearded Saki and Squirrel Monkey
in the igapó. My own observations combined with information from locals
indicate a strong migration of many of the primate species from the terra firme
to the igapó during the flood season, when the amount of fruit increases
substantially. However, I never saw Spider Monkeys in igapó, and
according to the locals, this species stays in the terra firme. This may also,
at least to some extent, be the case with the Tamarin.
Camera trapping
Camera trapping has been used successfully for mammal studies in
tropical forests of Asia and Africa (Griffiths and van Schaik 1993; Karanth and
Nichols 1998; Franklin et al. 1999). This survey, along with the studies
of Rittl (1998), Yabe and Higuchi (1998), and Yabe et al. (1998) has
shown that also in the Amazon camera trapping is a highly efficient way to
relatively quickly record a number of shy and secretive terrestrial mammal
species, and survey a fauna that may otherwise take years to inventory. The
above mentioned camera trapping studies north of Manaus recorded also
Jaguarundi, Ocelot, Margay, Grison, Coati, and a range of smaller species of
opossums and rodents.
Ants and termites are known to be a major problem for
field workers camera trapping in rainforest in Asia, since they use camera traps
as nesting sites. To solve this problem I recommend a simple solution: wrap
adhesive tape around the base of the pole on which the camera trap is placed
with the sticky side facing outwards. Above this, the bark can be peeled upwards
with a machete so that an ‘umbrella’ is constructed; this umbrella
protects the tape against rain and probably works against rodents (like the
system used on ropes on ships, to prevent rats from entering).
After this
study, a similar mammal survey was carried out in Pantanal of SW Brazil. In the
coming publication of that study (Trolle in prep.) more detailed recommendations
for camera trapping in the Amazon and Pantanal will be given.
ACKNOWLEDGEMENTS
This project was a collaboration between the Zoological Museum
University of Copenhagen, National Institute for Amazonian Research, Manaus
(INPA) and Museu Nacional, UFRJ, Rio de Janeiro. The project was made
economically possible by the generous support of WWF-Denmark/Novo Nordisk,
Explorers Club-US, Copenhagen Zoo, University of Copenhagen, Zoological Museum
of Copenhagen, Frimodt-Heineke Fonden, Torben og Alice Frimodts Fond, H.R.
Frederiksen og Grete Siim Frederiksens Fond, Direktør Peder Mortensen og
Hustru Marry Mortensens Fond, Kjebi Fonden, NetTravel, Duracell, Photographica,
and Fuji. Thanks are also due to Associação Amazônia for
providing the opportunity to carry out the study in Xixuaú Nature
Reserve. For collaboration, advice and support thanks to Dr. João Alves
de Oliveira, Dra. Maria Nazareth Ferreira da Silva, Dr. Hans J. Baagøe,
Prof. Jon Fjeldså, Mogens Andersen, Dr. Leila M. Pessôa and Dr.
Louise Emmons. Tim Dempster and João Alves de Oliveira kindly revised the
manuscript and Signe Zacchi translated the summary into French. And finally,
many thanks are extended to my field assistants in Xixuaú for invaluable
help in the field.
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