SciELO - Scientific Electronic Library Online

 
vol.49 número3-4Una nueva especie de rana de cristal del género Hyalinobatrachium (Anura: Centrolenidae) del Delta del Río Orinoco, VenezuelaUna nueva especie de serpiente del género Sibon (Serpentes: Colubridae) de la vertiente del Caribe de Costa Rica índice de autoresíndice de materiabúsqueda de artículos
Home Pagelista alfabética de revistas  

Servicios Personalizados

Revista

Articulo

Indicadores

Links relacionados

Compartir


Revista de Biología Tropical

versión On-line ISSN 0034-7744versión impresa ISSN 0034-7744

Rev. biol. trop vol.49 no.3-4 San José dic. 2001

 

Distribution and abundance of four caiman species (Crocodylia: Alligatoridae)
in Jaú National Park, Amazonas, Brazil
*

George Henrique Rebêlo 1 and Luciana Lugli 2

1 Instituto Nacional de Pesquisas da Amazônia, Coordenação de Pesquisas em Ecologia, Caixa Postal 478, 69011-970 Manaus-AM, Brazil. Phone: 55 92 6431820. E-mail: jacare@inpa.gov.br

2 Universidade Estadual Paulista, Rio Claro-SP, Brazil. Phone: 55 19 5332952. E-mail: llugli@ms.rc.unesp.br

* This study is dedicated to the memory of our friend, the Brazilian herpetologist and political activist Glória Moreira [1963-1997].

Received 17-I-2000. Corrected 03-X-2000. Accepted 08-II-2001.

Abstract

Jaú National Park is a large rain forest reserve that contains small populations of four caiman species. We sampled crocodilian populations during 30 surveys over a period of four years in five study areas. We found the mean abundance of caiman species to be very low (1.0 ± 0.5 caiman/km of shoreline), independent of habitat type (river, stream or lake) and season. While abundance was almost equal, the species’ composition varied in different waterbody and study areas. We analysed the structure similarity of this assemblage. Lake and river habitats were the most similar habitats, and inhabited by at least two species, mainly Caiman crocodilus and Melanosuchus niger. However, those species can also inhabit streams. Streams were the most dissimilar habitats studied and also had two other species: Paleosuchus trigonatus and P. palpebrosus. The structure of these assemblage does not suggest a pattern of species associated and separated by habitat. Trends in species relationships had a negative correlation with species of similar size, C. crocodilus and P. trigonatus, and an apparent complete exclusion of M. niger and P. trigonatus. Microhabitat analysis suggests a slender habitat partitioning: P. trigonatus was absent from river and lake Igapó (flooded forest), but frequent in stream Igapó. This species was the most terrestrial and found in microhabitats similar to C. crocodilus (shallow waters, slow current). Melanosuchus niger inhabits deep, fast moving waters in different study areas. Despite inhabiting the same waterbodies in many surveys, M. niger and C. crocodilus did not share the same microhabitats. Paleosuchus palpebrosus was observed only in running waters and never in stagnant lake habitats. Cluster analysis revealed three survey groups: two constitute a mosaic in floodplains, (a) a cluster with both M. niger and C. crocodilus, and another (b) with only C. crocodilus. A third cluster (c) included more species, and the presence of Paleosuchus species. There was no significant difference among wariness of caimans between disturbed and undisturbed localities. However, there was a clear trend to increase wariness during the course of consecutive surveys at four localities, suggesting that we, more than local inhabitants, had disturbed caimans. The factors that are limiting caiman populations can be independent of human exploitation. Currently in Amazonia, increased the pressure of hunting, habitat loss and habitat alteration, and there is no evidence of widespread recovery of caiman populations. In large reserves as Jaú without many disturbance, most caiman populations can be low density, suggesting that in blackwater environments their recovery from exploitation should be very slow.

Key words: Reptilia, Crocodylia, Amazonia, abundance, richness, wariness, Jaú National Park, Brazil.

 

Jaú National Park (JNP) is the world’s largest rain forest reserve, located in Central Amazonia, in a nearly pristine condition. A declining human population of a thousand people inhabit the area and take its subsistence from the forest. Most of them live in ten small villages, and some are scattered throughout the area. Their staple foods are fish, turtles and manioc; their subsistence is supplied by products that they extract to sell. Main products are liana faggots, brazil nuts, copaíba oil, cassava flour, live turtles, aquarium fishes and timber (Guazelli et al. 1998). Water bodies are predominantly poor nutrient blackwater environments that may affect plant richness and floristic composition of the igapó (flooded forest) (Ferreira 1997). The rains are abundant and the dry season short. As is common in other central Amazonia areas, the forest is flooded during rainy season and the isolated pools dry up when rains are scarce (Richards 1996).

The crocodilian assemblage is composed of four Alligatoridae species (blunt head and armoured crocodilians). Species interactions of amazonian crocodilians are poorly known and studies examining patterns of that community have controversial conclusions (Medem 1971, Magnusson 1985). Two gregarious species inhabit quiet waters of great rivers and lakes: Melanosuchus niger (Spix, 1825) and Caiman crocodilus (Linnaeus, 1758). Studies discovered that Melanosuchus is absent from many areas of historic distribution, and this had been related to commercial hunting (Medem 1971, 1981, 1983, Brazaitis et al. 1990, 1996a, b).

Two other species are the solitary, small, and heavily armoured caimans of the genus Paleosuchus Gray, 1862: Paleosuchus trigonatus (Schneider, 1801) observed in running waters and forest streams, and the dwarf P. palpebrosus (Cuvier, 1807) widely distributed throughout savannas and forests streams. They are sympatric species in some localities, but exclusive in other areas (Medem 1971, 1981, 1983). The thick bony plated skin of Paleosuchus is considered a successful adaptation to terrestrial life (Medem 1981); since it is not suitable for tanning, commercial hunting for this skin is low.

We found a rather small caiman population in JNP in a survey through different areas, habitats, and seasons. Crocodilian po-pulations of 1-10 individuals/km were more frequently reported, while very dense populations (more than 10 individuals/km) were less frequently observed in different parts of the world (see Glastra 1983, Montague 1983, Gorzula and Paolillo 1986, Seijas 1986, Bayliss 1987, Gorzula and Seijas 1989, Espinosa 1995, Brazaitis et al. 1996b, Mohd Sah and Stuebing 1996, Da Silveira et al. 1997). We examined the patterns of abundance and ecological relationships among sympatric caimans in JNP, combining descriptive data with community analysis techniques described by Ludwig and Reynolds (1988).

We investigated specifically: (1) the caiman species abundances, diversity, and the similarities between surveys, (2) the caiman species assemblage structure, (3) the human impact on caiman populations, (4) and the sizeage structures, which are important demographic parameters for conservation.

 

Materials and methods

Study area: The study was conducted during 1993 and 1996 at Jaú National Park, situated 200 km Northwest from Manaus, Amazonas State, Brazil (1º00’-3º00’S, 61º30’-64º 00’W). In 1980, the Jaú River and its riparian areas up to the banks of the Unini and Carabinani rivers were established as a National Park (Act nº 85.200) to preserve their biological and cultural values. Because few rivers in Amazonia have this level of protection, the JNP provides an opportunity to study crocodilian assemblages and their habitat associations along a relatively undisturbed river. JNP has 22 720 km 2 . The climate is wet tropical (Köppen Af), with rainy and dry seasons, the mean annual temperature ranges between 24-26 °C, and the annual rainfall ranges between 1 750 and 2 500 mm. Rainfall occurs throughout the year, but the dry season is in July-November and the wet season is in December-June. The annual variation of river level is near 7 m, and the majority of the Igapó forest is flooded from 221 to 264 days each year (Anonymus 1998). The waters from the area have low conductivity, acid pH, low dissolved O 2 , and few suspended matter, with mean water temperature of 26.2 °C (Díaz-Castro 1999).

Sampling and data collection: The transects surveyed were selected within the JNP study areas targeted by eight fieldteams involved in the basic surveys to design the management plan of the reserve. We performed nocturnal spotlight surveys, on open water, riverbanks and shoreline areas, using aluminium boats (6 m) equiped with 15-25 HP outboard engines as the only platform.

We covered 231 km of the Jaú river and tributaries in three areas and times: (i) Cutiaú (October 1993, March 1994, January 1996), (ii) Central (July 1993, January and February 1994), (iii) West (January 1996). We covered also 111 km of (iv) Rio Negro and the Jaú mouth (July and October 1993, April and September 1995), and 28 km of (v) the Unini River and tributaries, in north JNP (September 1996).

To evaluate human impact we compared abundances between less and more disturbed areas. Less disturbed or rarely accessible to non-dwellers, include all Jaú river areas (i, ii, and iii), and more disturbed areas (with regular traffic of regional ships and most active trade of manufactured and extractive products) include the Jaú mouth, Rio Negro (iv) and Unini river (v).

We extensively searched the waters of JNP to find the caimans. Surveys were conducted at night, begining 1 hr after sunset. Caimans were located by eye-reflection using hi-powered spot-lights (powered by a 12 volts car battery). We moved slowly toward the animals to identify species, estimate sizes, and then captured a sample of animals to correct for size estimates. Acommon sampling error is imprecise size estimates (Magnusson 1983). Based on size measurements of animals, we produced a regression equation relating measured total lenght (M) to estimated total length (E).

The length of the survey routes were determined in two ways: (a) by standing the limits from geographical references established during fieldwork, or (b) by ploting precise geographical coordinates obtained with the Global Positioning System Receiver Garmin® 45. The distances traveled were measured on a drawn map of JNP (produced by Fundação Vitória Amazônica-FVA, based on Landsat-TM images), with flexible ruler (in mm), and converted to scale. Caiman abundance was expressed as the number of animals of each species (excluding hatchling pods) seen per kilometer.

We identified the species in the field by direct observation of morphologic characteristics of at least three living animals: head shape, jaw pattern, and body color. The animal sizes (total lengths) were estimated at distances < 10 m.

Assemblage analysis: The impact of human presence was evaluated by comparison of the differences in the proportion of unidentified caimans (eye proportion = wariness) between less and more disturbed areas and during survey series conducted in four localities. Often, the animals fled before our approach and were classified as eyes. These constituted the main proportion of eyes reported, but some eyes represented animals spoted inside inaccessible Igapó covering. We do not summed eyes to abundance of any other species, as in other studies (e.g. Seijas 1988, Da Silveira et al. 1997). The dominant species can be different for different surveys, so we chose to analyse eyes apart; too many eyes-only observations may result in a common bias in crocodilian surveys (Bayliss 1987), but can indicate the isturbance level of localities and wariness (Pacheco 1996, Ron et al. 1998). We followed the suggestion of Ron et al. (1998) that stated that an increase in the proportion of eyes reflects an increase in wariness and a behavioral response to human disturbance.

To examine habitat partitioning we identified habitat patches and microhabitats that we could easily categorize. Each survey was designed to represent only one of four habitat categories: lake, river, river- lake, and stream. These categories are self-explaining, except river-lake, that refers solely to long islands, with great lakes inside and separated by wide channels (Figs. 1, 2). For every individual caiman encountered, we assigned one of nine microhabitat classifications (considering vegetation type, water depth and flow) designated as: (1) Grass: constitutes the floating grass carpet; (2) Rapids: include shallow waters with swift running current; (3) Pool: deep waters with no current; (4) Deep: the deep waters with swift moving currents; (5) Stream Igapó: flooded forest with little current, short flooding period, and high plant diversity; (6) Land: all land locations including animals on sandbank, mud beaches, rocks, and clay banks; (7) Margins: shallow waters with little or no current; (8) Lake Igapó: flooded forest with no current, longest flooding period, and lowest plants richness; (9) River Igapó: flooded forest with little current, but intermediate flooding period and plant richness.



For search of species associations, we constructed a presence-absence matrix with surveys as columns and caiman species as rows, and then calculated Jaccard Distance (JD) as follows:

1-2W/(A+B-W)

where W is the sum of shared abundances and A and B are the sums of abundances in individual sample units.

We used another matrix of quantitative measures of species abundance (surveys as columns and species as rows) to identify species correlations (covariation of abundances between species) (Ludwig and Reynolds 1988). We used Spearman correlation coefficients to determine species affinities. All indexes, calculations and statistical tests, were performed using Systat 5.03 (Anonymous 1990-1993).

We used Cluster analysis to examine crocodilian assemblage structure (an uncommon procedure, since crocodilian studies usually were focused on one species), because this classification technique places similar samples or surveys into groups or clusters. These clusters may delimit or represent different crocodilian assemblages based on their overall resemblance. A possible random utilization of resources can be indicated by no structure. But if there are any ecological separations and associations between species, well-defined clusters of surveys can emerge using hierarchical, agglomerative and polythetic classifications with species abundance data, which can be summarized in a dendrogram (Ludwig and Reynolds 1988). The data of abundances matrix were added to a constant (0.01), logtransformed and relativized by standard deviates of species abundances. The distance measure used was relative euclidian and the group linkage method was median. Cluster analyses were performed using Pc-ord 2.01 software (McCune and Mefford 1995). Voucher specimens were deposited in the herpetology collection of the Instituto Nacional de Pesquisa da Amazônia in Manaus, Brazil.

 

Results

Distribution and abundance: During the sampling, we identified 290 individuals. Species observed were common caiman (C. crocodilus), black caiman (M. niger), Schneider’s caiman (P. trigonatus), and dwarf caiman (P. palpebrosus). Common caiman was the most frequently observed (69 %), followed by black caiman (14 %), Schneider’s caiman (12 %), and dwarf caiman (4 %) across all surveys combined (Table 1).

 

Table 1

Numbers of crocodilians sighted withing species and size classes in Jaú National Park
during 1993-1996 nocturnal spotlight surveys.

Numbers in size classes*

Species

N

H

2 - 6

6 - 10

10 - 14

14 - 18

18 - 22

> 22

NR

Caiman crocodilus

201

44

25

53

38

28

7

1

5

Melanosuchus niger

40

8

 

4

5

3

6

11

3

Paleosuchus trigonatus

36

 

 

14

11

8

 

 

3

Paleosuchus palpebrosus

13

 

2

3

8

 

 

 

 

  * Size classes in m x 10-1. N: total crocodilians sighted. H: hatchlings. NR: no size estimated.
 
The abundances of species varied across surveys (Table 2). We surveyed 371 km of shoreline, 287 km during the wet season (20 surveys) versus 84 km in the dry season (10 surveys). The total number of caimans (i.e., all species combined) observed in the dry season surveys (1.1 + 0.5 caimans/km) was greater than in the wet season (0.9 + 0.5 caimans/km), but these differences were not significant between seasons (t 0.05(2),28 = 0.829, p > 0.5). The higher abundance (2.3 caimans/km, two species, stream habitat) was observed in wet season. The second highest abundance (2.2 caimans/km, one species, lake habitat) was observed in dry season.

 Table 2

Surveys of caimans in Jaú National Park.

 

Surveys

Dates

H (hours)

Habitat

Study

km

Season

 

 

Caimans/km

 

 

Hatchlings

 

 

 

 

Type

Area

 

 

CC

MN

PP

PT

Eyes

Total

Pods

count

1

Jaú mouth

Jul,17,93

04:00

River

RN

11.7

W

0.43

0.08

0.00

0.00

0.17

0.68

 

 

2

Miratucu

Jul,19,93

03:23

Stream

CE

21.6

W

0.00

0.00

0.00

0.78

0.21

0.99

 

 

3

C.Grande-Miratucu

Jul,29,93

02:15

River

CE

11.0

W

0.45

0.00

0.00

0.00

0.54

0.99

 

 

4

Preto

Oct,19,93

02:20

Stream

RN

4.9

D

0.82

0.00

0.20

0.20

0.41

1.63

 

 

5

Preto mouth-Manichuau

Oct,20,93

01:11

River

RN

8.3

D

0.36

0.00

0.00

0.00

0.36

0.72

 

 

6

Supiá Lake

Oct,20,93

00:32

Lake

RN

4.9

D

2.04

0.00

0.00

0.00

0.20

2.24

 

 

7

Cutiuaú Lake

Oct,29,93

04:02

Lake

CT

11.5

D

0.96

0.26

0.00

0.00

0.09

1.31

 

 

8

Miratucu (lower)

Jan,17,94

02:12

Stream

CE

9.0

W

0.00

0.00

0.00

0.89

0.22

1.11

 

 

9

Miratucu mouth-Catoá

Jan,17,94

03:32

River

CE

7.7

W

0.78

0.13

0.13

0.00

1.04

2.08

1

8

10

Macaco

Jan,23,94

01:12

Stream

CE

9.3

W

0.54

0.32

0.00

0.00

0.32

1.19

 

 

11

Umanapana

Jan,24,94

02:10

Stream

CE

6.4

W

0.00

0.00

0.31

0.62

1.41

2.34

 

 

12

Macaco mouth-Maranhoto

Jan,30,94

03:01

River

CE

21.6

W

0.37

0.00

0.00

0.00

0.28

0.65

 

 

13

Miratucu mouth-Pajé

Feb,15,94

02:53

River

CE

20.1

W

0.20

0.00

0.05

0.00

0.05

0.30

 

 

14

Miratucu (Gerley)

Feb,18,94

03:00

Stream

CE

14.0

W

0.00

0.00

0.14

0.36

0.50

1.00

 

 

15

Moura-Nazaré

Mar,05,94

03:05

Lake

CT

12.4

W

0.89

0.00

0.00

0.00

0.32

1.21

2

16

16

Uruá-Jaú mouth

Sep,02,94

01:00

River

RN

4.0

D

0.25

0.75

0.00

0.00

0.25

1.25

 

 

17

Negro

Apr,06,95

03:12

River

RN

14.3

W

0.35

0.00

0.00

0.00

0.14

0.49

 

 

18

Negro (Enseada)

Apr,07,95

02:36

River/ Lake

RN

18.5

W

0.05

0.16

0.00

0.00

0.00

0.21

 

 

19

Negro (Panema)

Apr,08,95

05:34

River/ Lake

RN

24.5

W

0.53

0.00

0.00

0.00

0.28

0.81

2

8

20

Negro (Onças)

Apr,09,95

04:22

River/ Lake

RN

32.3

W

0.22

0.03

0.00

0.00

0.28

0.53

 

 

21

Jaú mouth

Apr,10,95

03:00

River

RN

14.3

W

0.21

0.07

0.00

0.00

0.56

0.84

1

3

22

Negro (Grande)

Sep,01,95

04:01

River/ Lake

RN

21.6

D

0.37

0.00

0.00

0.00

0.37

0.74

 

 

23

S.Maria-Praia Alta

Jan,19,96

02:37

River

WE

12.3

W

0.16

0.00

0.08

0.00

0.16

0.40

 

 

24

S.Maria-Feijão

Jan,23,96

02:33

River

WE

5.9

W

0.17

0.34

0.17

0.00

0.51

1.19

 

 

25

Pinto

Jan,21,96

01:50

River

WE

13.6

W

0.22

0.22

0.00

0.00

0.29

0.73

2*

9

26

Cutiuaú Lake

Jan,25,96

01:18

Lake

CT

6.5

W

0.15

0.00

0.00

0.00

0.46

0.61

 

 

27

Unini (Sumaúma)

Sep,05,96

01:43

Lake

U

1.2

D

0.00

0.00

0.00

0.00

0.81

0.81

 

 

28

Papagaio

Sep,11,96

01:06

River

U

12.0

D

0.08

0.16

0.00

0.00

0.25

0.50

1

4

29

Unini (Tapiira)

Sep,14,96

01:54

River/ Lake

U

7.7

D

0.65

0.00

0.00

0.00

0.52

1.17

 

 

30

Mauaru

Sep,17,96

02:10

Stream

U

7.7

D

0.13

0.13

0.00

0.00

0.26

0.52

 

 

 H: duration of observation period, CC: Caiman crocodilus, MN: Melanosuchus niger, PP: Paleosuchus palpebrosus, PT: Paleosuchus trigonatus. Study areas: RN: Rio Negro, CE: Central, CT: Cutiaú, WE: West, U: Unini. Seasons: W: wet season, D: dry season. * including one pod of M. niger hatchlings.

Therefore the mean caiman abundance was 1.0 + 0.5 caimans/km. Low abundance surveys predominated: in 17 surveys we counted less than 1.0 caiman/km, while in eight surveys we observed moderate abundances (1.0-2.0 caiman/km). The highest abundances were observed in less disturbed areas, while the lowest abundances were observed in more disturbed areas. The ranges of abundances were similar between rivers (0.3-2.1 caimans/km), lakes (0.6-2.2 caimans/km) and streams (0.5-2.3 caimans/km), but was minor in riverlake surveys (0.2-1.2 caimans/km).

No caiman species were distributed continuously across the entire study area. The common caiman ocurred in 25 surveys (mean abundance 0.4 + 0.3 caimans/km), the black caiman was observed in 12 surveys (0.2 + 0.1 caimans/km), Schneider’s P. trigonatus was observed only in five surveys (but with mean abundance of 0.6 + 0.3 caimans/km), and P. palpebrosus was observed in seven surveys (mean of 0.1 + 0.1 caimans/km).

Comparing the species composition between surveys we found two groups: C. crocodilus - M. niger, and P. t r igonatus - P. palpebrosus (Fig. 3). Despite the coefficient of community does not take into account the relative abundance of species assemblage, we measured the differences in community structure and expressed the relative weakness of the two possible associations, the pair C. crocodilus - M. niger (0.480) and the pair P. trigonatus - P. palpebrosus (0.333), and revealed that there is no association (or complete exclusion) between M. niger and P. trigonatus.


Similarity among surveys may be expressed by measuring the correlation between species abundances. There was a small negative correlation between C. crocodilus and P. trigonatus that was significant (-0.459, ANOVA 1,27 F = 5.501, p = 0.027) and a positive, but not significant (0.401, p = 0.08) correlation between P. palpebrosus and P. trigonatus. There was a small covariation of C. crocodilus and M. niger abundances that was highly non-significant (0.004, p = 0.900). The structure of caiman assemblage does not ressemble a pattern of separated sets of species associated to specific habitats. The only actual trend we observed in species relationships was that populations of similar size species (C. crocodilus and P. trigonatus) were mutually excludents and may have a niche overlap.

Size-age structures: In order to correct estimated total length of observed, and not captured animals, a linear regression line of predicitive size was used for all species (M = 0.004 + 0.966 E, F 1,18 = 60.046, p < 0.001, R 2 = 0.757) (Fig. 4). Frequency distributions of estimated size for black caiman and dwarf caiman were skewed toward the larger size classes, which were expected for long-lived species with continual growth. Large M. niger include some 4 m long individuals, while large P. palpebrosus has animals of 1.0-1.4 m in length. The length frequencies for C. crocodilus showed a predominance of juveniles and subadults, and for P. trigonatus a predominance of middle size classes of subadults.


Few juveniles were observed. Among common caiman, eight pods of hatchlings were observed, 22 % of individuals of these species were juveniles, most observed in the early wet season (six pods in Rio Jaú and one pod in Rio Negro), and one in early dry season (Rio Unini). Common caiman pods were observed in nearly every habitat type, but mostly in river habitats. Juveniles composed 20 % of the overall observations of black caiman, that corresponds to one pod of hatchlings observed in upper Jaú in the early wet season. No juvenile Schnider’s or dwarf caimans were observed.

Species-habitat relations: Comparing the species composition between surveys using coefficients of community (Jaccard) for habitat categories, we found differences. Ranking the mean coefficients for habitat, the most similar were (1) lakes, (2) lakes and river-lakes, and (3) river-lakes (inhabited by the C. crocodilus - M. niger pair). Moderately similar were (4) rivers and river-lakes, (5) rivers and lakes, and (6) rivers (inhabited by C. crocodilus -M. niger pair, with occasional P. palpebrosus). Dissimilarities were higher among (7) streams, (8) rivers and streams, (9) streams and river-lakes, and (10) streams and lakes.

Surveys in streams were not quite homogeneous, they were different within stream surveys and different in each stream, among upper and lower courses of the stream. In some stream surveys, we found P. trigonatus populations, but in others we did not.

The examination of microhabitats used by caimans (Fig. 5) suggests a thin habitat partitioning. Paleosuchus trigonatus were absent from river and lake Igapó, but were frequent in stream Igapó. This species was the most terrestrial and frequently observed on land. The only microhabitat category that they used as frequent as C. crocodilus were margins. However, P. trigonatus was frequently observed in water as deep as M. niger.



Fig. 5. Microhabitat used by caimans in Jaú National Park. CC = Caiman crocodilus, MN = Melanosuchus niger, PP =
Paleosuchus palpebrosus, PT = Paleosuchus trigonatus, I. = Igapó.

The most frequently used microhabitat by C. crocodilus and M. niger were river and lake Igapó, but this two species differ in use of other microhabitats: C. crocodilus predominate in shallow waters (margins) and land locations, while M. niger predominated in deep moving waters, but were absent from stream Igapó. Carpets of floating grass are rare in JNP and only C. crocodilus was observed in such habitat.

Paleosuchus palpebrosus was observed only in running water microhabitats: river Igapó, margins, stream Igapó and rapids, and never in stagnant waters of lake habitats. Only Paleosuchus was observed in fast running rapids.

The general pattern of microhabitat use was strongly oriented to river Igapó, lake Igapó and margins (30 %, 20 %, and 18 % of observations, respectively).

Assemblage structure: The patterns of clustering of surveys were summarized in the dendrogram in Fig. 6. Using an arbitrary cutoff distance of 4.3, we distinguish three clusters, which can be described only by species composition: Cluster A represents surveys where we find C. crocodilus and M. niger. Cluster B represents surveys where we find only C. crocodilus populations. Both patterns were common and observed in all habitats types and study areas, making a mosaic. Cluster C represents some of the most rich in species surveys, but what was distinctive was the presence of at least one Paleosuchus in all these surveys, in river and stream habitat types, in Central and West study areas. Populations of P. trigonatus were find only in streams, and P. palpebrosus in river and streams.


Fig. 6. Cluster analysis of surveys of caimans of Jaú National Park, based on the abundance data of Table 2. Data added to a constant (0.01), log-transformed and relativized by standard deviates of species abundances. Distance measure was relative euclidian and group linkage method was Median. Percent chaining: 7.53. Clusters: A: surveys with Melanosuchus niger and Caiman crocodilus set, B: surveys with only Caiman crocodilus, C: surveys with at least one Paleosuchus species. Survey number legend as Table 2.

Human impact: Long term human disturbance of this ecosystem was not much evident. We observed a mild slight trend to increase wariness, that could be attributed to human general activities in JNP. The proportion of eyes observed in much disturbed localities (40 %) was greater than in little disturbed ones (38 %), but this diference was not significant (t 0.05(2),28 = 0.269, p > 0.5). We observed, however, an increase of wariness that could be attributed to our surveys. When we compared the proportion of eyes in consecutive surveys, there was a trend to increase the proportion of wariness with time in all habitats and study areas, considered by us disturbed or not. Three sequences of three surveys (surveys # 1, 16, and 21 in Jaú mouth, surveys # 2, 8, and 14 in Miratucu stream, and surveys # 7, 15, and 26 in Cutiaú lake) and one sequence of five surveys (# 17, 18, 19, 20, and 22 in Rio Negro), all showed clearly similar increasing wariness trends.

 

Discussion

This study focused on distribution and abundance of the caiman community of Jaú National Park as they related to habitat caracteristics. The presence and relatively stable abundance of common species at each study site show that these species had wide distributions along the area. However, the abundance of each species varied in association with different habitats and as a response to species interactions. The small relative abundances could reflect bias due to wet season dispersal, since in JNP environmental disturbance are minimal, and there is no marginal habitats. Differences between dry and wet seasons surveys could indicate the existence of many individuals unapparent in the wet season.

Caiman surveys in South American savannas observed large differences of abundance between seasons, and the dry seasons abundances could be two to ten times larger than the wet season abundances (e.g. Gorzula 1978, Glastra 1983). But the similar numbers between dry and wet seasons in JNP, suggests that there should not be a great number of caimans hidden inside the flooded forest. Juveniles of C. yacare have been reported to occur somewhat appart from adults and in shallower waters (e.g. Rebêlo et al. 1997). However, we assumed that because the same survey method and similar effort were used among surveys, observational bias remained consistent and the observed differences in abundances for each species likely reflects the caiman assemblage structure in JNP.

The very low densities of fewer than 1 caiman/km that we detected were reported in 70 % of the localities surveyed elsewhere in Amazonian waters by Brazaitis et al. (1996a). To compare this study with published surveys carried out in Amazonian waters, Glastra (1983), Espinosa (1995), Brazaitis et al. (1996a), Da Silveira et al. (1997) and Da Silveira and Thorbjarnarson (1999) reported values between 1- 19, 0-2, 0-10, 0-58 and 1-115 caimans/km, respectively. The abundance obtained in this study (0-2 caimans/km) was low in comparison with the majority of values from other caiman surveys in Amazonian waters. But, abundances reported by Da Silveira and Thorbjarnarson (1999) of very abundant populations of C. crocodilus and M. niger in Mamirauá reserve sector’s where hunting pressure is lowest, is a rare event in Amazonia.

The distribution of common caimans reflects their general habitat use as was seen in other studies (Medem 1971, 1981, 1983, Magnusson 1985, Brazaitis et al. 1990, 1996a, b). Surveys where we observed only one species always had C. crocodilus in floodplain, or P. trigonatus in streams of the Central study area. Melanosuchus niger and P. trigonatus were not observed together in any survey, maybe because of mutual exclusion, although the literature recorded sympatric occurrence of the two species (Medem 1967).

In previous studies M. niger populations were so reduced, that it was impossible to determine which is the relationship between that species and C. crocodilus (Brazaitis et al. 1996a, Da Silveira et al. 1997). The authors explained the small numbers as evidence of very reduced populations due to commercial hunting: few M. niger survivors were observed "mixed" with several C. crocodilus, which could be contributing (as predators or competitors) to hinder the recovery of the populations of M. niger submitted to hunting (Magnusson and Rebêlo 1982, Rebêlo and Magnusson 1983). However, without strong evidences of species interference, differences in distribution of sympatric populations were attributed to habitat preferences (Magnusson 1985). Therefore, reduced populations of M. niger were considered unable to affect the distribution of C. crocodilus (Da Silveira et al. 1997), while the reversal is unknown.

The different adult size of the two species and the differential use of microhabitats, could reduce or attenuate the negative effects of sharing the same habitats and eating similar preys. In the blackwater Archipelago of Anavilhanas, C. crocodilus abundance does not coincide with food availability and nesting areas of M. niger, which predominate in the deeper water channels, with more sediments and floating grass (Da Silveira et al. 1997).

The non occurrence of the four species in all surveys suggests effective habitat partitioning. Melanosuchus niger and C. crocodilus inhabit floodplain habitats, while P. trigonatus inhabits forest streams and turbulent waters (Medem 1981, 1983), and their peculiar diet was attributed to habitats selection (Magnusson et al. 1987). Notwithstanding, our results of streams with C. crocodilus and M. niger challenge strictly the habitat separation hypothesis, despite the absence of P. trigonatus in river and lake habitats. The importance of interspecific competition in the organization of crocodilian communities is easy to imagine since they are members of the same guild, but is difficult to establish since the mere presence of differences of resource utilization between species is not evidence of competition (Schoener 1974), and if other factors (as predation, food, weather, or something else) keep densities at a low level, the role of competition will be negligible (Begon et al. 1996).

Physiological and behavioral mechanisms can also reduce or attenuate the niche overlap between species. Nests of P. t r igonatus need an extra source of heat (Magnusson et al. 1985) while the C. crocodilus females build common mound nests (Gorzula and Seijas 1989). Adults of C. crocodilus prey upon fishes and large invertebrates, while adults of P. trigonatus prey mostly on terrestrial vertebrates (Magnusson et al. 1987). Paleosuchus trigonatus have a highly terrestrial life (Magnusson and Lima 1991) while C. crocodilus spend most of the day in the water (Marcellini 1979).

We observed P. trigonatus in 71 % of the stream surveys. Medem (1967, 1971) remarked that what separate the species is any skill to deal with water speed: in his analysis Paleosuchus are caimans of (1) running waters of tropical forest streams with rocky or sandy bottom, (2) neighbourhood of rapids, water- falls, jumps and whirls, (3) narrow channels of large rivers through where masses of water slide swiftly (as in narrow pass), and (4) savanna streams and gallery forests.

For Medem (1967, 1971), P. trigonatus would represent the primitive form, while P. palpebrosus would be the most specialized. Paleosuchus palpebrosus would have developed adaptations to colonize the larger bodies of water, where there is some water flow (as a secondary effect, the "carapace" guaranteed an extra protection against drying up in unfavorable habitats and against predation from larger species).

If the flow is the critical factor, the resistance to impact on rocks and the swimming capacity would be factors capable to increase or to reduce the fitness of a species. Magnusson (1989) commented that "It is obvious that the habitats of each [Paleosuchus] differ, and that the habitats of both are different from those of other sympatric crocodilians but just which differences are critical remains conjecture." According to Magnusson (1989), P. trigonatus is the specialized form differing from the other crocodilians in its thermal biology (living in moderate temperature and relatively stable forest habitat, with limited opportunities for basking), and may be the largest biomass of great predators in the Terra Firme forest near Manaus, drained by small streams (Magnusson and Lima 1991).

In JNP, P. trigonatus is not the only species of forest streams, and different from the Manaus area, most of the individuals we observed were subadults, a stage of life with high dispersion rates (great mobility). In the Manaus semi-urban area, most of the population was constituted by adult animals, whose high survival rate and extended lifetime would have great influence on the population dynamics (Magnusson and Lima 1991).

Conservation: We used a regression line to correct size estimates, a usually neglected tool. The action plan for crocodilian conservation of the Crocodile Specialist Group (Thorbjarnarson 1992), call for more population survey work, that was "urgently needed for a large percentage of the [crocodilian] species". Surveys were considered needed not only for planning recovery programs, but also as the first step of sustainable yield utilization projects. However, rarely the relationship between actual and estimated sizes of individuals has been presented, and accurate estimates of total numbers are of limited use without some idea of the accuracy of the size estimates (Magnusson 1983).

These data provide the first comprehensive overview of the caiman community in JNP. For common and black caimans in this areas, populations are currently widespread in floodplain, but appear to be not abundant. Schnider’s caiman is specific of some streams. The rare but widespread observation of dwarf caiman suggest that the species is a habitat generalist, but its abundance may be affected by the other species. Their use of the river, however illustrates the importance of riverine systems to all caiman species found within JNP.

The differences in numbers of different species show the influence of different habitat caracteristics and patterns on caiman assemblages. The river and lake Igapó were important to common and black caimans, the deep waters attracted more black caimans, and the stream Igapó and rapids were preferred by Paleosuchus.

Very low numbers of caimans were present in JNP , but the observation of pods of hatchlings suggests that there is successful reproduction of the two most abundant species. Without immediate threats of habitat destruction, with large areas of pristine habitats, the situation has been favorable for the recovery of the populations affected by commercial hunting in the past. The international trade in caiman skins periodically increase the demand for all crocodilian-skin products, touted by the fashion industry (Brazaitis et al. 1998). The regional market for caiman meat is increasing (Da Silveira and Thorbjarnarson 1999) and current evidences of localized recovery are supporting a proposal to downlist M. niger in Brazil (Ronis da Silveira pers. comm.). As large caiman populations are rarely found, we do not support the increase of utilization of M. niger and the efforts to widespread use of the species.

The discovery of small populations of M. niger in scattered distributions throughout Amazonia, are considered an effect of overexploitation (Plotkin et al. 1983, Brazaitis et al. 1996a, b, 1998), and does not fit the historical records that reported larger populations (Bates 1876, Carvalho 1951, Aguirre 1956). Small, disjunct, isolated populations that are reported do not mean that the species has recovered everywhere and can not support the efforts to reassessment of the status of the species and allow it in the trade.

We do not know what was the level of disturbance that the caimans of JNP experienced in the past. If measures of wariness reflect such disturbance (and we agree that it may reflect very recent episodes), our study shows that researchers disturbed the caimans more than local inhabitants. Based on reports of local inhabitants, we can say that where today is the JNP, commercial hunting of C. crocodilus and M. niger stopped in 1973. This could be consequence of legal prohibition or depletion of population stocks.

Current inhabitants cause little impact on caiman populations, but this is not because there is hunting restriction, since it is also forbidden the commercial fishing of turtles. They catch turtles once there is market for them. Now, local inhabitants rarely eat caiman meat, or kill large and potentially dangerous animals. However, when the fashion comes back, we must be aware about the management and conservation of the low density populations in poor blackwater areas.

The aquatic ecosystems of the Amazonia blackwater rivers and streams constitute nutrient poor areas, considered uncapable to maintain populations as large as the ones reported for "white waters" (loam silted rivers).

Blackwater rivers are considered acid, low nutrient, high nitrogen ecosystems with head-waters inside forests with sandy podzols soils (Sioli and Klinge 1962). Blackwater rivers and the lands they drain have low subsistence potential for human populations and they are notorious "starvation rivers" (Meggers 1996). As top predators even the caiman populations should be limited by habitat productivity. Small populations have a general problem in conservation biology, since they can be at risk simply because of their size, which requires studies on the effects of low numbers on population persistence (Caughley and Gunn 1996). Thus the factors that are limiting these populations, however, can be independent of human exploitation.

Currently, in Amazonia increased the pressure of hunting, habitat loss and habitat alteration, and there is no evidence of widespread recovery of caiman populations. Our data show that in large reserves without many disturbances, most caiman populations can have low density, suggesting that in blackwater environments their recovery from exploitation should be very slow.

 

Acknowledgments

We thank the following: Regina Oliveira invited us to work at JNP. Laércio Marajó dos Reis, Aldenora Lima de Queiroz, José Carlos Raposo, Carlos Sotero da Silva, Carola Reimann and Norma Chemin helped us in the fieldwork. Arnaldo Carneiro Filho gave to us files of the Landsat-TM images. Augusto S. Abe and Peter Brazaitis reviewed carefully our text, and two anonymous reviewers read critically an early version of this paper. This research was supported by: Fundação Vitória Amazônica; Instituto Nacional de Pesquisas da Amazônia; Biodiversity Support Program - a consortium among World Wildlife Fund, The Nature Conservancy and World Resources Institute, financed by Usaid (Grant MS33); Fundação O Boticário de Proteção a Natureza (Projeto de Pesquisa 119/93A); Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (Bolsa de Doutorado para GHR); and Instituto Brasileiro do Meio Ambiente e dos Recursos Naturais Renováveis. This paper is part of GHR doctorate thesis in Ecology at Universidade Estadual de Campinas.

 

References

Aguirre, A. 1956. Contribuição para o estudo da biologia do jacaré-açú Melanosuchus niger (Spix). Ministério da Agricultura - Divisão de Caça e Pesca, Rio de Janeiro. 15 p.        [ Links ]

Anonymous. 1990-1993. Systat 5.03 for windows. Evanston, Illinois.        [ Links ]

Anonymous. 1998. Plano de manejo do Parque Nacional do Jaú. Fundação Vitória Amazônica, Manaus. 258 p.        [ Links ]

Bates, H.W. 1876. The naturalist on the river Amazons. John Murray, London. 300 p. (Tradução Regina R. Junqueira)        [ Links ]

Bayliss, P. 1987. Survey methods and monitoring within crocodile management programmes, p. 157-75. In G. Webb, C. Manolis & P. Whitehead (eds.). Wildlife management: Crocodiles and Alligators. Surrey Beatty, Chipping Norton, Australia.        [ Links ]Begon, M., J.L. Harper & C.R. Townsend. 1996. Ecology: Individuals, populations and communities. Blackwell Science, Oxford. 952 p.         [ Links ]

Brazaitis, P., C. Yamashita & G.H. Rebêlo. 1990. A summary report of the CITES central South American caiman study: Phase I: Brazil, p. 100-115. In Crocodiles. Proceedings of the 9th Working Meeting of Crocodile Specialist Group, IUCN - The World Conservation Union, Gland, Switzerland.        [ Links ]

Brazaitis, P, G.H. Rebêlo & C. Yamashita. 1996a. The status of Caiman crocodilus crocodilus and Melanosuchus niger populations in the Amazonian regions of Brazil. Amphibia-Reptilia 17: 377-385.        [ Links ]

Brazaitis, P, G.H. Rebêlo, C. Yamashita, E.A. Odierna & M.E. Watanabe. 1996b. Threats to brazilian crocodilian populations. Oryx 30: 275-284.        [ Links ]

Brazaitis, P., M.E. Watanabe & G. Amato. 1998. The caiman trade. Sci. Amer. 278: 52-58.        [ Links ]

Carvalho, A.L. 1951. Os jacarés do Brasil. Arq. Mus. Nac. (R. Janeiro) 42: 125-139.        [ Links ]

Caughley, G. & A. Gunn. 1996. Conservation biology in theory and practice. Blackwell Science, Cambridge. 459 p.        [ Links ]

Da Silveira, R., W.E. Magnusson & Z. Campos. 1997. Monitoring the distribution, abundance and breeding areas of Caiman crocodilus crocodilus and Melanosuchus niger in the Anavilhanas Arquipelago, Central Amazonia, Brazil. J. Herpetol. 31: 514-520.        [ Links ]Da Silveira, R. & J.B. Thorbjarnarson. 1999. Conservation implications of commercial hunting of black and spectacled caiman in the Mamirauá Sustainable Development Reserve, Brazil. Biol. Conserv. 88: 103-109.         [ Links ]

Díaz-Castro, J.G. 1999. Biomassa, diversidade e fatores abióticos controladores do bloom de ficoperifíton no canal central do rio Jaú, na época da cheia, Parque Nacional do Jaú – Amazônia central. Tese de Doutorado, Instituto Nacional de Pesquisas da Amazônia / Universidade do Amazonas, Manaus.        [ Links ]

Espinosa, J.A.V. 1995. Estado poblacional, utilización de tipos vegetacionales y crecimiento de Melanosuchus niger y Caiman crocodilus (Crocodylidae: Alligatorinae) en Zancudococha y Cuyabeno, Amazonia Ecuatoriana. Tesis de Licenciado, Pontificia Universidad Catolica del Equador, Quito.        [ Links ]

Ferreira, L.V. 1997. Effects of the duration of flooding on species richness and floristic composition in three hectares in the Jaú National Park in floodplain forests in central Amazonia. Biodivers. Conserv. 6: 1353-1363.        [ Links ]

Glastra, R. 1983. Notes on a population of Caiman cocodilus crocodilus depleted by hide hunting in Surinam. Biol. Conserv. 26: 149-162.        [ Links ]Gorzula, S. 1978. An ecological study of Caiman crocodilus crocodilus inhabiting savanna lagoons in the Venezuelan Guayana. Oecologia 35: 21-34.         [ Links ]

Gorzula, S. & A. Paolillo. 1986. La ecología y el estado actual de los aligatóridos de la Guayana Venezolana, p. 37-54. In Crocodiles. Proccedings of the 7th Working Meeting of the Crocodile Specialist Group. IUCN, Gland, Switzerland.        [ Links ]

Gorzula, S. & A.E. Seijas. 1989. The common caiman, p. 44-61. In P. Hall & R. Bryant (eds.). Crocodiles: Their ecology, management, and conservation. IUCN Publ. New Series, Gland, Switzerland.        [ Links ]

Guazelli, A.C., G.H. Rebêlo, J.H. Benatti, M.R. Pinheiro, M.P.S.R. Chaves, M. Saragoussi, R. Oliveira da Silva, S. Borges & H. Barreto. 1998. A gênese de um plano de manejo: O caso do Parque Nacional do Jaú. Fundação Vitória Amazônica, Manaus. 114 p.        [ Links ]Ludwig, J.A. & J.F. Reynolds. 1988. Statistical ecology: A primer on methods and computing. Wiley, New York. 337 p.         [ Links ]

Magnusson, W.E. & G.H. Rebêlo. 1982. Brazilian crocodiles: The problems of conservation in a multispecies system. Zimbabwe Sci. News 17: 56-57.        [ Links ]

Magnusson, W.E. 1983. Size estimates of crocodilians. J. Herpetol. 17: 86-88.        [ Links ]

Magnusson, W.E. 1985. Habitat selection, parasites and injuries in Amazonian Crocodilians. Amazoniana 9: 193-204.        [ Links ]

Magnusson, W.E., A.P. Lima & R.M. Sampaio. 1985. Sources of heat for nests of Paleosuchus trigonatus and a review of crocodilian nest temperatures. J. Herpetol. 19: 199-207.        [ Links ]

Magnusson, W.E., E. Silva & A.P. Lima, 1987. Diets of Amazonian crocodilians. J. Herpetol. 21: 85-95.         [ Links ]

Magnusson, W.E. 1989. Paleosuchus, p. 101-109. In P. Hall & R. Bryant (eds.). Crocodiles: Their ecology, management, and conservation. IUCN Publ. New Series, Gland, Switzerland.        [ Links ]

Magnusson, W.E. & A.P. Lima, 1991. The ecology of a cryptic predator Paleosuchus trigonatus in a tropical rainforest. J. Herpetol. 25: 41-48.        [ Links ]

Marcellini, D.L. 1979. Activity patterns and densities of Venezuelan caiman Caiman crocodilus and pond turtles Podocnemis vogli, p. 263-271. In J.F. Eisenberg (ed.). Vertebrate ecology in the northern Neotropics. Smithsonian, Washington.        [ Links ]

Mc Cune, B. & Mefford, M.J. 1995. PC-ORD. Multivariate analysis of ecological data - Version 2.01. MjM Software, Gleneden Beach, Oregon.        [ Links ]

Medem, F. 1967. El género Paleosuchus en Amazonia, p. 141-162. In Atas do Simpósio sobre a Biota Amazônica 3 (Limnologia). Superintendência para o Desenvolvimento da Amazônia, Belém.        [ Links ]

Medem, F. 1971. Biological isolation of sympatric species of South American Crocodilia, p. 152-158. In Crocodiles. IUCN Publ. New Series, Suppl. Paper. Medem, F. 1981. Los Crocodylia de Sur America 1. Colciencias, Bogotá. 354 p.        [ Links ]

Medem, F. 1983. Los Crocodylia de Sur America 2. Colciencias, Bogotá. 270 p.        [ Links ]

Meggers, B.J. 1996. Amazonia: Man and culture in a counterfeit paradise. Smithsonian, Washington. 214 p.        [ Links ]

Mohd Sah, S.A. & R.B. Stuebing. 1996. Diet, growth and movements of juvenile crocodiles Crocodylus porosus Schneider in the Klias River, Sabah, Malaysia. J. Trop. Ecol. 12: 651-662.        [ Links ]

Montague, J.J. 1983. Influence of water level, hunting pressure and habitat type on Crocodile abundance in the Fly river drainage, Papua New Guinea. Biol. Conserv. 26: 309-339.        [ Links ]

Pacheco, L.F. 1996. Wariness of caiman populations and its effect on abundance estimates. J. Herpetol. 30: 123-126.        [ Links ]

Plotkin, M.J., F. Medem, R.A. Mittermeier & I.D. Constable. 1983. Distribution and conservation of the black caiman (Melanosuchus niger), p. 695-705. In A.G.J. Rhodin & K. Miyata (eds.). Advances in herpetology and evolutionary biology. Museum of Comparative Zoology, Cambridge.        [ Links ]

Rebêlo, G.H. & W.E. Magnusson. 1983. An analysis of the effect of hunting on Caiman crocodilus and Melanosuchus niger based on the sizes of confiscated skins. Biol. Conserv. 26: 95-104.        [ Links ]

Rebêlo, G.H., G.A.N. Borges, C. Yamashita & A.G. Arruda Filho. 1997. Growth, sex ratio, populations structure, and hunting mortality of Caiman yacare in the Pantanal, Brazil. Vida Silv. Neotrop. 6: 29-36.        [ Links ]

Richards, P.W. 1996. The tropical rain forest: An ecological study. Cambridge University, Cambridge. 575 p.        [ Links ]

Ron, S.R., A. Vallejo & E. Asanza. 1998. Human influence on the wariness of Melanosuchus niger and Caiman crocodilus in Cuyabeno, Ecuador. J. Herpetol. 32: 320-324.        [ Links ]

Schoener, T.W. 1974. Resource partitioning in ecological communities. Science 185: 27-39.        [ Links ]

Seijas, A.E. 1986. Situación actual de las poblaciones de babas y babillas (Caiman crocodilus) en la región nortecostera de Venezuela, p. 28-36. In Crocodiles. Proccedings of the 7 th Working Meeting of the Crocodile Specialist Group. IUCN, Gland, Switzerland.        [ Links ]

Seijas, A.E. 1988. Habitat use by american crocodile and the spectacled caiman coexisting along the Venezuelan coastal region. M.Sc. Thesis, University of Florida, Gainesville. 104 p.         [ Links ]Sioli, H. & H. Klinge, 1962. Solos, tipos de vegetação e águas na Amazônia. Bol. Mus. Paraense Emílio Goeldi, N. S. 1: 27-37.         [ Links ]

Thorbjarnarson, J. 1992. Crocodiles: An action plan for their conservation. IUCN, Gland, Switzerland. 136 p.        [ Links ]

Creative Commons License Todo el contenido de esta revista, excepto dónde está identificado, está bajo una Licencia Creative Commons