This article outlines a coastal mammalian harvesting pattern involving a few terrestrial mammals whose biomass appears to have been greater when associated with man than under "natural" conditions. By concentrating the supply of both carbohydrates and animal protein, "garden hunting" may have eliminated seasonality and scheduling problems. Because it artificially increased the biomass of selected animals, it may have functioned as a substitute for animal domestication.
This article outlines a coastal mammalian harvesting pattern involving a few terrestrial mammals whose biomass appears to have been greater when associated with man than under "natural" conditions. By concentrating the supply of both carbohydrates and animal protein, "garden hunting" may have eliminated seasonality and scheduling problems. Because it artificially increased the biomass of selected animals, it may have functioned as a substitute for animal domestication.
This article outlines a coastal mammalian harvesting pattern involving a few terrestrial mammals whose biomass appears to have been greater when associated with man than under "natural" conditions. By concentrating the supply of both carbohydrates and animal protein, "garden hunting" may have eliminated seasonality and scheduling problems. Because it artificially increased the biomass of selected animals, it may have functioned as a substitute for animal domestication.
Source: Human Ecology, Vol. 4, No. 4 (Oct., 1976), pp. 331-349 Published by: Springer Stable URL: http://www.jstor.org/stable/4602380 . Accessed: 16/05/2014 11:48 Your use of the JSTOR archive indicates your acceptance of the Terms & Conditions of Use, available at . http://www.jstor.org/page/info/about/policies/terms.jsp . JSTOR is a not-for-profit service that helps scholars, researchers, and students discover, use, and build upon a wide range of content in a trusted digital archive. We use information technology and tools to increase productivity and facilitate new forms of scholarship. For more information about JSTOR, please contact support@jstor.org. . Springer is collaborating with JSTOR to digitize, preserve and extend access to Human Ecology. http://www.jstor.org This content downloaded from 132.248.9.8 on Fri, 16 May 2014 11:48:26 AM All use subject to JSTOR Terms and Conditions Human Ecology, Vol. 4, No. 4, 1976 "Garden Hunting" in the American Tropics Olga F. Linares1 Using faunal analysis, this article outlines a coastal mammalian harvesting pat- tern involving a few terrestrial mammals whose biomass appears to have been greater when associated with man than under "natural" conditions. Archeologi- cal evidence suggests that these animals fed regularly on cultivated crops and were hunted in house gardens and cultivated fields. By concentrating the supply of both carbohydrates and animal protein, "garden hunting" may have elimi- nated seasonality and scheduling problems. And because it artificially increased the biomass of selected animals, it may have functioned as a substitute for animal domestication. KEY WORDS: hunting; tropics; faunal collections; coastal settlements; prehistoric hunting. INTRODUCTION Students of tropical South American cultures often draw a distinction between societies located near important rivers and societies occupying "mar- ginal" habitats away from the mainstreams (Sauer, 1958; Cameiro, 1964, 1970; Lathrap, 1968, 1970; Morey, 1970; Meggers, 1971). Nonriverine groups are con- sidered to be agriculturally impoverished, as well as committed, in the absence of fishing possibilities, to the permanent quest for easily depleted terrestrial and arboreal game. Low population densities, small group size, settlement dis- persal, and constant movement are thought to result from this mode of life (Carneiro, 1970). All nonriverine peoples were not, however, necessarily equally restricted. Numerous Indian groups were encountered by the first European explorers along both American seacoasts, but these have been discounted or ignored in the literature, possibly because these groups were rapidly decimated (see Sauer, 1966). Yet archeologists have repeatedly shown that coastal settlements flou- Smithsonian Tropical Research Institute, P.O. Box 2072, Balboa, Panama Canal Zone. 331 i 1976 Plenum Publishing Corporation, 227 West 17th Street, New York, N.Y. 10011. No part of this publication may be reproduced, stored in a retrieval system, or transmitted, In any form or by any means, electronic, mechanical, photocopying, microfilming, recording, or otherwise, without written permission of the publisher. This content downloaded from 132.248.9.8 on Fri, 16 May 2014 11:48:26 AM All use subject to JSTOR Terms and Conditions 332 Linares rished in the tropics from at least 3000 B.C. onward. The subsistence system of these settlements must have been very different from those of inland groups. In fact, terrestrial hunting among these groups tended not toward a broad-spectrum "many species taken" adaptation but rather toward greater specialization and selectivity. A prehistoric example of selective hunting by otherwise maritime groups has been described by Coe and Flannery (1964), while Nietschmann (1973) has discussed hunting among the present-day turtle-fishing Miskito Indians of coastal Nicaragua. The garden-hunting pattern I describe here from a site called Cerro Brujo in Bocas del Toro province, Panama, is also a specialized one and selectivity is indicated by the archeological remains. Rather than resembling tropical forest hunting, with its particular technology, its belief system, and male-oriented trekking activities (Siskind, 1973; Murphy and Murphy, 1974), this game-procure- ment system was more akin to harvesting vegetable products and maritime re- sources. The contrast between animal biomass under natural conditions and biomass under garden hunting is marked. Shifting cultivation, especially of cultivated root crops, affects the' biomass of terrestrial mammals that are behaviorally preadapted to becoming commensals of man. As a kind of mammalian "tending pattern," garden hunting may have taken the place of animal domestication in parts of the New World tropics. Both patterns result in the substitution of culturally created for naturally existing mammalian biomasses. Even now, after the introduction of bamyard animals and cash crops, garden hunting remains a widespread and important practice. THE SETTING Bocas del Toro (hereafter designated as Bocas) is a long and narrow prov- ince located on the northwest sector of the Isthmus of Panama, facing the Caribbean Sea or Atlantic Ocean (Fig. 1). Climatically, Bocas is wet (The Af tropics in Koppen's classification), with two very short, relatively dry seasons. The mean annual rainfall averaged for 5 years is 3703 mm (about 148 inches), with little seasonal variation and with most precipitation falling at night, thus limiting transpiration. Topographically, Bocas is characterized by low, rolling hills and ridges that extend to the water's edge. There are neither broad coastal plains nor many beaches. The archeological site of Cerro Brujo is found toward the tip of the small Aguacate Peninsula, away from major rivers but accessible to two lagoons (Fig. 2). The "community pattern" represented is that of a dispersed hamlet con- sisting of four localities marked by shell-midden clusters. Within the hamlet unit, the localities nearest each other were 300 m apart; the two most distant were This content downloaded from 132.248.9.8 on Fri, 16 May 2014 11:48:26 AM All use subject to JSTOR Terms and Conditions "Garden Hunting" in the American Tropics 333 T3 cr 96 z C4 'S E 'S 0 !7 = E w < < M 'IT Z 3c C .C Cld U Cd CO QC CIS C's 0 -4 ...... . ... .............. .3 co This content downloaded from 132.248.9.8 on Fri, 16 May 2014 11:48:26 AM All use subject to JSTOR Terms and Conditions 334 Linares Fig. 2. Looking into Almirante Bay from a ridge on the Aguacate Peninsula. 800 m apart. We have calculated the adult residential population at Cerro Brujo as approximately 25 persons (Linares and Ranere, 1971; Linares, 1970). The principal biotopes utilized by the Cerro Brujo and other Aguacate inhabitants can be listed as follows: 1. Terrestrial biotopes: (1) Ridgetops between the 80 and 140 m contours were used for habitation and possibly for small kitchen gardens and tree crops. (b) The 40 and 80 m contour was probably used for swidden fields. (c) Streams flowing through the base of the ridges provided the only source of fresh water and were probably favorite spots for garden- ing and hunting. (d) Low-lying swamps are used nowadays to collect crabs and to gather palm products. These are difficult areas to traverse. 2. Littoral or marine biotopes: (a) Mangrove stands and mud flats fringing the shore were used for gathering two species of Ostrea, two species of Arca, and a species of d7ama. This is also the natural habitat of the caiman, which was occasionally hunted. (b) From shoreline to about 2 fathoms, or approximately 4 m, are coral outcrops, barrier reefs, and other habitats where most inshore fishing took place. (c) Offshore beyond 2 fathoms are found larger pelagic fish, most of which were not taken, suggesting that the open sea was mostly used for green turtle fishing and for transportation. This content downloaded from 132.248.9.8 on Fri, 16 May 2014 11:48:26 AM All use subject to JSTOR Terms and Conditions "Garden Hunting" in the American Tropics 335 The bulk of the cultural materials excavated at Cerro Brujo came from two main midden clusters (Fig. 3), representing a brief occupation. Five radio- carbon estimates fall between A.D. 960 and A.D. 985. A 20-30 year occupa- tion accords well with the time span of a contemporary Guaymi hamlet. Close similarities exist between the oldest of the Cerro Brujo artifacts and those from a number of sites in the neighboring highlands of Chiriqui province (see Linares et al., 1975). I have suggested elsewhere (Linares, in press) that the Cerro Brujo inhabitants migrated to their peninsular setting from landlocked interior habitats. This hypothesis is corroborated by the absence of molluscs in the oldest levels, as well as by the close chronological and spatial overlaps. A thorough survey of the Aguacate Peninsula in 1973 revealed only three additional archeological sites. These resemble Cerro Brujo in size, layout, and chronology (Fig. 4). Each site was made up of several dwelling localities, marked by shell-midden refuse deposits, found within an area 1.5-2 km in diameter. Since each loose cluster of localities was separated from similar units by tracts of un- inhabited territory, I am assuming that each corresponded to a dispersed hamlet (what Young, 1971, calls a caseri'o among the modern Guaymi who inhabit this area). These ancient hamlets were usually located on the highest ridges of the Aguacate Peninsula, at spots with both lagoons in view. Population densities over the entire peninsula at A.D. 900 can be roughly estimated as no more than 3 persons per square kilometer. Fig. 3. Aerial photograph of the principal Cerro Brujo shell-midden cluster in process of excavation. (Lower trench is 10 by 6.5 m.) This content downloaded from 132.248.9.8 on Fri, 16 May 2014 11:48:26 AM All use subject to JSTOR Terms and Conditions 336 Linares (CA-1,-2, -4). Except for a deforested zone along the only major alluvial areas in Bocas (the Changuinola-Sixaola on the west and the Cricamola on the east), the prov- ince presents a mosaic of small clearings in the midst of extensive forested tracts. The vegetation is typically a "dense growth of large, predominantly broad-leaf evergreen, trees" (Gordon, 1969: 5) mixed with a few deciduous species. Before proceeding, we must consider in some detail whether the ecology of the area today is similar to that of late pre-Columbian times. (For places referred to in this discussion, see Fig. 1.) Scholars have argued quite persuasively that much of the New World tropics was heavily populated and extensively cultivated in late prehistoric times (Gordon, 1957; Sauer, 1966; Dobyns, 1966; Bennett, 1964; Lathrap, 1970). Some areas, however, were not, and the interfiuvial zone bordering Almirante Bay, including the Aguacate Peninsula, seems to have been one of the This content downloaded from 132.248.9.8 on Fri, 16 May 2014 11:48:26 AM All use subject to JSTOR Terms and Conditions "Garden Hunting" in the American Tropics 337 relatively undisturbed regions.2 Given the limitations of the early Spanish des- criptions of Panama (Howe, 1974: 12-18; Young, 1970), we must turn to archeology for evidence of population distribution and man-induced vegeta- tional changes at the time of occupation of the Bocas sites. The shell mounds of Almirante Bay and Chiriqui Lagoon were first de- scribed by Gordon (1961), who concludes, in a later publication, that the "shell collectors must have been numerous . . ." (Gordon, 1969: 67). Although Gordon's description of the Bocas environment is invaluable, his archeological interpretations may be misleading. Most of the shell-middens described (Gordon, 1961: map 2; 1969: map 4, p. 68) are very small. They are not to be taken as archeological "sites" (i.e., hamlet clusters in this context), but as dwelling localities or garbage dumps, to be exact-some of them associated with at most a single house. (Thus, while Gordon's map indicates nine "sites" in Aguacate Peninsula, our survey shows only four dispersed hamlets.) Furthermore, these localities were probably occupied only for a short time. Incidentally, in the years between our excavations of Cerro Brujo and a systematic survey of Aguacate Peninsula, the Guaymi Indian family living in the vicinity of our site, much in the manner of their ancestors (Linares, 1970), has shifted residence twice, abandoning an old house and building two new structures. All this has taken place in 3 years, within a radius of less than 1 km, and is a normal procedure in the developmental cycle of the Guaymi domestic group (Young, 1971). There is little evidence, then, that in the late prehistoric period Almirante Bay or its immediate vicinity was much more heavily populated or disturbed by man than it is now. This impression is strengthened by the palynological record. None of the 18 samples prepared for analysis from one of the two cores collected from freshwater bogs about 100 m from the Cerro Brujo hamlet con- tained pollen of agricultural plants: "Pollens which may indicate disturbance, cheno-ams, composites, Cecropia sp. and grasses are rare in the samples ex- amined .... With a cursory look such as this it appears that there is no record of forest disturbance by man in the Core CBII" (West, n.d.: 1), or at least no record of major disturbances over a long period of time. THE CERRO BRUJO FAUNA: SOME CULTURAL INFERENCES Over 6000 mammal bones were recovered from the shell-containing (i.e., more recent) of the two occupations at the Cerro Brujo site. These, plus other animal bones, make up 15,000 specimens altogether. Grayson (1973) has 2A careful reading of Fernando Colon's account of his father's fourth voyage in 1502 (re- produced in Lothrop, 1950: 3-7) conflrms this point. Although he mentions encounter- ing Indians in Almirante Bay, the only places where he talks about towns and many peoples are in Catiba, Zobrare, etc. These places are about 200 km to the east of Almirante Bay, in northern Veraguas province. This content downloaded from 132.248.9.8 on Fri, 16 May 2014 11:48:26 AM All use subject to JSTOR Terms and Conditions 338 Linares classified the mammals into 1437 identifiable specimens belonging to 14 species (excluding man) and then calculated the "minimum numbers of individuals" of each species. Keeping in mind that there are difficulties with this method,3 we can pi ceed with our analysis. Table I suggests that the Cerro Brujo inhabitants had strong hunting preferences for certain species. Agouti (Dasyprocta punc- tata), paca (Cuniculus paca), and nine-banded armadillo (Dasypus novem- cintus) together constitute 80.9% of all animals taken. Four large species-collared peccary (Tayassu tajacu), white-lipped peccary (Tayassu pecari), white-tailed deer (Odocoileus virginianus), brocket deer (Mazama americana)-are less impor- tant, amounting to 10. 1% of the total. The rats (Sigmodon, Oryzomys, Hoplomys) and the opossums (Caluromys, Marmosa) together add up to only 6.8% of the total number of minimum individual mammals. The manatee (Trichechus man- atus), an aquatic mammal, is only 1.9% of the total.4 Table I may convey the impression that small mammals were the only im- portant components of the Cerro Brujo diet; however, any such impression is dispelled if we convert these values to butchered weights (Table II) and add up the values for the same species as grouped above. Conversion to butchered weights changes the percentages considerably, and it is obvious that in reckoning "cultural importance" both measures are needed to draw conclusions.5 The two methods become more disparate when the smaller (or the larger) animals are compared. This is exaggerated in the case of agoutis and manatees. Both of these animals were probably equal in importance: the caviomorph rodents (agouti and paca) were important for regular consumption and the manatee for intermittent con- sumption. Whether their combined presence is calculated in individual numbers 'The minimum numbers method (MNI for short) determines the necessary number of in- dividuals of a species accounting for all identical bone elements found in a given collec- tion. Using the Cerro Brujo fauna, Grayson (1973) demonstrated that the MNIs vary significantly depending on the analytic units used for the calculations. He compared MNIs calculated on the basis of single excavation strata with MNIs calculated on the basis of the whole site. Neither of these alternatives is entirely satisfactory. Therefore, White (n.d.), at my request, reanalyzed the Cerro Brujo fauna and calculated MNIs on the basis of nine "features" representing activity loci within a dwelling locality. As expected, he came out with more accurate values, halfway between those obtained by Grayson. Nonetheless, since both methods yielded a similar rank order for the most important species, I have used Grayson's MNI figures based on the single strata distinctions because these figures are published, and because I consider them to be the less distorting of the alternatives he presents. Skeptics should keep in mind that differential bone preservation, distribution, and destruction, to say nothing about differences in cultural practices (hunting techniques, taboos, food preferences), necessarily affect a-ll faunal analysis-as indeed they affect all kinds of prehistoric reconstructions. 4R. White (n.d.) recalculated the percentages for each of these species clusters as (a) 7 3.8%; (b) 16.8%; (c) 7.4%; (d) 0.9%. He is also of the opinion that, of the two, only the collared peccary was present in the Cerro Brujo fauna. This strengthens the thesis of this article. 5White (n.d.) would rank the most important species by butchered weight in the following order of decreasing importance: Tayassu, Odocoileus, Cuniculus, Trichechus, Dasyprocta, and Dasypus. This rank order strengthens the argument that small mammals were not the only ones taken by the Cerro Brujo group. This content downloaded from 132.248.9.8 on Fri, 16 May 2014 11:48:26 AM All use subject to JSTOR Terms and Conditions "Garden Hunting" in the American Tropics 339 Table I. List of Mammals Hunted by the Prehistoric Cerro Brujo Inhabitantsa Number of Minimum Species English name specimens numbers Percent Dasyprocta punctata Agouti 822 204 43.8 Cuniculus paca Paca 224 104 22.3 Dasypus novemcintus Nine-banded armadillo 186 69 14.8 Tayassu tajacu Collared peccary 94 27 05.8 Sigmodon Cotton rat 28 16 03.4 Odocoileus virginianus White-tailed deer 20 14 03.0 Oryzomys Rice rat 16 11 02.4 Tayassu pecari White-lipped peccary 15 4 00.9 Hoplomys Armored rat 8 3 00.6 Didelphis narsupialis Opossum 5 1 00.2 Mazama americana Brocket deer 3 2 00.4 Caluromys Woolly opossum 2 1 00.2 Marmosa Mouse opossum 1 1 00.2 Trichechus manatus Manatee 13 9 01.9 Total 1437 466 aAdapted from Grayson (1973: Table 2, p. 436). Table II. Comparison of the Minimum Number of Individualsa with the Butchered Weight of the Most Important Mammals at Cerro Brujo Minimum Butchered weights number of Species individualsb Kilograms Pounds Percent of total Agouti 43.8 556 1224 16.7 Paca 22.3 709 1560 21.3 Nine-banded armadillo 14.8 219 483 06.6 Collared peccary 5.8 490 1080 14.8 Cotton rat 3.4 4.09 9 0.12 White-tailed deer 3.0 382 840 11.5 Rice rat 2.4 1 2.4 0.06 White-lipped peccary 0.9 91 200 2.73 Opossum 0.2 9 90 0.27 Woolly opossum 0.2 3.6 8 0.10 Mouse opossum 0.2 <2.0 <4.0 0.05 Brocket deer 0.4 36 80 1.09 Manatee 1.9 818 1800 24.60 aAdapted from Grayson (1973: Table 2, p. 436). bPercent of total. This content downloaded from 132.248.9.8 on Fri, 16 May 2014 11:48:26 AM All use subject to JSTOR Terms and Conditions 340 Linares Table III. Comparison of the Butchered Weights (i.e., meat without bones) of the Terrestrial Fauna Hunted by the Cerro Brujo Inhabitantsa with the Fauna Hunted by the Miskito Indians of Nicaraguab and the Bayano Cuna Indians of PanamaC Cerro Brujo Miskito area Bayano Cuna Species hunted (20-year span) (1-year sample) (14-day sample) Agouti 16.7 Insignificant Agouti Nine-banded armadillo 06.6 Not mentioned Insignificant Paca 21.3 Insignificant Paca Manatee 24.6 1.5% (Not here) Collared peccary 14.8 0.61% Collared peccary White-tailed deer 11.50 45.0% Not important White-lipped peccary 2.73 50.0% White-lipped peccary Brocket deer 1.09 0.30% Brocket deer Tapir None 2.0% Tapir, plus two kinds of monkeys, coati, tree squirrels aValues expressed as percentage of total butchered weights of all minimum number of individuals of all species in the collection. bData adapted from Nietschmann (1973: Tables 1 and 2). CData adapted from Bennett (1962: Table 6, p. 42). (1.3%) or in butchered weights (3.9%), deep-forest species such as the brocket deer and the white-lipped peccary are seen to have been insignificant. A further comparison can be made (Table III) between the butchered weights in the Cerro Brujo mammal sample and the butchered weights given for the same species hunted by the coastal Tasbapauni Miskito Indians of eastern Nicaragua (Nietschmann, 1973; I have extrapolated the information from his Tables 21 and 22). The last column in Table III of this article simply lists the terrestrial mammals hunted by the mainland, noncoastal, Bayano Cuna of eastern Panama (Bennett, 1962: Table 6, p. 42). Although few hard and fast conclusions can be drawn from Table III, the comparative data do support the idea that Cerro Brujo inhabitants harvested a different proportion of a faunal community than did the other groups. The abundant species at Cerro Brujo are of little im- portance to the Miskito Indians. In turn, the Bayano Cuna regularly hunt a num- ber of additional mammalian species. To summarize, hunting among each of these three peoples, the Bayano Cuna, the Miskito Indians, and the prehistoric Cerro Brujo group, differs greatly. The Bayano Cuna exploit the high canopy, as well as the deep forest, for game. On the other hand, the coastal Tasbapauni Miskito are maritime exploiters, partly as a result of the commercial demand for turtles. Although they hunt a number of other species, they focus on only two large terrestrial mammals (the white-lipped peccary and the white-tailed deer), which they track inland during a specified season. In the Cerro Brujo case, a considerable amount of game was provided by six species (Table III), but only three species were regu- This content downloaded from 132.248.9.8 on Fri, 16 May 2014 11:48:26 AM All use subject to JSTOR Terms and Conditions "Garden Hunting in the American Tropics 341 n 4 cn AO 0 'C 0 u E C) C) 11!; E w 0 00 C> cn cn eq P', 0 0 z 0 00 oq 0 0 W; C; C> 0 0 U S v 73 0 0 CA w C) CD C) 4) (O C) -4 C) C) E -S :3 W) vt 0 C) Z 0 0 CA 00 C) C) C4 M n C W) cl W) 0 -0 CA 1.0 W rl- CD cn E '-t -4 " %D 0 -, 0 I--, 0 -4 tn -4 %O tn 00 r 0 0 0 0 ." 'O w C: - pq m W) 0 0 1-4 oq 00 0 o 0 0 cq C) >.. ZZ o tz-, t cq , - +.- ON 0 u 0 o r- 00 tn 0 0 0 0 Its w > en 00 tn --I tn eq C) %C O %O CD r 0 o o Z C 00 C:) o 00 cq O C) eq C) u ON - 4-4 CD en r- %O m en %O 0 -.4 4.4 -0 0 00 eq %O 4n oo 4.4 00 en 00 00 00 ..4 6.4 C) ON IOJ m J:,. = E0 Cd w C,; C; t,; r4 0 cd w Ca 4-4 6-4 0 0 w ON r- 404 6-10 I", C.-4 CA rA 0 w 0-4 coi 0 4. O .2 04 0 4.4 -5 O 0 C-3 Irk) 413 cj ct w bo Cd p Zs 0 8. , l:L t3 lu This content downloaded from 132.248.9.8 on Fri, 16 May 2014 11:48:26 AM All use subject to JSTOR Terms and Conditions 342 Linares larly caught (see Table I). An idea of just how much terrestrial game was being taken is provided by the next comparison. Faunal assemblages from archeological sites are assumed by faunal ana- lysts to represent the products of cultural selection - samples that are biased under human hunting pressures. Rarely, however, has anyone attempted to measure just how far a cultural faunal assemblage departs from "normal" spe- cies distributions in undisturbed habitats. In the present case, we can rearrange the data on Table I and calculate the biomass of the terrestrial animals in the Cerro Brujo collection.6 This procedure may facilitate comparison between a "cultural faunal assemblage" and the same assemblage in two "natural," i.e., undisturbed, habitats (Table IV). Table IV suggests that the biomass for every species represented in the collection is significantly higher in our site than is their biomass in nature. The proposition may be entertained that the product of 20 years of casual hunting is somehow equivalent to having recovered a complete sample of all the indi- vidual animals of a certain species found in each of two "natural" habitats at any one point in time. This proposition is obviously very difficult to test. None- theless, Table IV gives us some relative idea of "cultural" vs. "natural" biomass: (1) The percentage biomasses of the three most common species in our Cerro Brujo collection (agouti, paca, and armadillo) together amount to 52.9% of the total. In the Surinam situation, the figure for the same species is 12.7%. In Barro Colorado Island (BCI) it is 19.4%, assuming that the biomass for Dasypus is more or less the same as in Surinam. (2) The collared peccary alone accounts for 21.68% of the Cerro Brujo biomass, while it is only 3.5% of the total in Surinam and 3.5% in BCI. (3) The biomass of white-tailed deer at Cerro Brujo was much higher than at BCI (compare 19.5 5% with 0.6%). If we now take into consideration the full data presented by Eisenberg and Thorington (1973) for all terrestrial and arboreal mammalian species (the bats excepted) in Surinam and BCI, and compare these with those for our faunal collection of mammals, we see that at those two localities not one of the most dominant mammals (in terms of biomass) appears in our collections. This suggests that the Cerro Brujo people were being extremely selective, or that they did not develop appropriate hunting techniques. They seem to have been ignor- ing many of tl'e following common animals: (1) the two-toed sloth (Choleopus sp.) and the three-toed sloth (Bradypus sp.); (2) monkeys of several genera (Cebus, Ateles, Alouatta, etc.); (3) tapir (Tapirus sp.); (4) the spiny rat (Pro- echimys sp.), one of the most abundant of the New World tropical rodents 'I have used Eisenberg and Thorington's (1973) method for calculating biomass. This in- volved multiplying the numbers of individual animals by the live weight of an "average" adult specimen and then calculating the percentage biomass of each species in the Cerro Brujo collection. The difficulties with using average-weights are illustrated by the fact that Eisenberg and Thorington (1973: Table 1, p. 152) and Nietschmann (1973: Table 20, p. 165) present slightly different live weights for the same species. This content downloaded from 132.248.9.8 on Fri, 16 May 2014 11:48:26 AM All use subject to JSTOR Terms and Conditions "Garden Hunting" in the American Tropics 343 Cd > CZ cl 7:$ Cd 0 +.,- lt U -4 > Cd cl ci .4 : :z 0 Cd ct 0 C, Cd 4.1 Cd 4.1 VD cl cl O Cd Cd CZ 0 0 M 0 Ct z > cd cld cld 0 m U 4) C) U (L) to +-- - 00 00 lr $..4 . z cti cri C6 04 cts Cd Cld Cd 4--j C13 O cd 7:1 C) > 03 Cd 04 cl C's 0 C--.4 4 r. = C6 0 = =S -4 C) C14 0 VI C) cn 05 0 CA C4 w 0 0 0 x x cl CIS t4-4 W5 w C13 1-4 0 -4 4-1 cn 0 0 C-) Q Cld Cd (D 4 'A 0) Cts 40 bo 40. 0 0 C) Cd (D 6 C4M : V .2 4' C's -t:3 to 0 0 CIS 0 1-4 0 Cd Cld 10 Cd C) Co Cj 1:1 0 41 C's0 0 Cq Cd z z z C z M 0 P", C) cn t3 -4 Cld F 7:1 Cd cl 4-A "Cl (L) 0 4.1 j ...q U 0 t3 4 u ;3 N Cd 0 CZ -11 9L4 L) 1:13 45 This content downloaded from 132.248.9.8 on Fri, 16 May 2014 11:48:26 AM All use subject to JSTOR Terms and Conditions 344 Linares (Gliwicz, 1973); (5) the coati (Nasua sp.), as well as squirrels (Sciuridae) and raccoon (Procyon). The absence of these animals in our collection cannot be due to simple deforestation or game depletion. As I have indicated, one must assume that the land was at least as forested then as it is now. Furthermore, some of these animals, e.g., coatis, would have flourished in second growth. By compiling a list of the main behavioral traits of terrestrial mammals appearing in our Cerro Brujo collection (Table V), and considering the habits and habitats of the mammals that do not appear in the refuse of this site, we can see two things. The most abundant animals present are either smallish ani- mals that live in the underbrush or in burrows, often in the vicinity of encamp- ments or recently cleared fields (the caviomorph rodent and armadillo), or larger forms that are not too shy and live - or can live - in forest-edge conditions (the collared peccary and the white-tailed deer). The mammals missing altogether or poorly represented are either those that inhabit the high canopy (monkeys, sloths) or those that are fast climbers (coatis, squirrels) or those that are very shy and live in forested conditions away from man (the brocket deer and the tapir). In short, although large forest tracts must have existed in Bocas at that time, the Table VI. List of Fish, Amphibians, and Reptiles from Cerro Brujoa Minimum Species Colloquial name numbers Percentage Megalops-Albula Tarpon 6 2.2 Belonidae Needlefish 7 2.6 Centropomus Snook 53 19.3 Serranidae Grouper (sea bass) 53 19.3 Carangidae Jack 21 7.7 Lutjanus Snapper 38 13.9 Haemulon Grunt 10 3.6 Sparidae Porgies 3 1.1 Sciaenidae Drums (corvina) 1 0.4 Sparus sp. Parrotfish 4 1.5 Eleotridae Gobies 3 1.1 Kyphosus Rudderfish 1 0.4 Sphyraena Barracuda 6 2.2 Diodontidae Porcupine fish 16 5.8 Rays Rays 5 1.8 Sharks Sharks 2 0.7 Anuran Frogs 7 2.6 Crocodilian Caiman 5 1.8 Geoemyda Forest turtle 1 0.4 Chelonidae Sea turtle 19 6.9 aAdapted from a list by Wing (n.d.). The minimum number of in- dividuals is given only for the most recent of the two occupations. This content downloaded from 132.248.9.8 on Fri, 16 May 2014 11:48:26 AM All use subject to JSTOR Terms and Conditions "Garden Hunting" in the American Tropics 345 Cerro Brujo inhabitants were concentrating on species that live in forest-edge conditions and readily invade man-made clearings. Evidence supporting the idea that this specialization was facilitated by the presence of alternative protein sources from the sea is given in Table VI. The total minimum number of individual fish, reptiles, and amphibians in Table VI, having been calculated on a different basis from that of Grayson (1973), although on the same basis as that of White (see footnote 4), appears to be smaller than that of mammals. But marine fishing may have been even more important than terrestrial hunting (White and Wing, personal communications). In fact, Cerro Brujo people were capable of taking in large, and sometimes dangerous, aquatic organisms. The most common edible species in Table VI (Centropomus, serranid, carangid, Lutianus) also grow very large. Missing from the collection are the open-water pelagic fish that swim rapidly, such as the tuna and the mackerel. The most common fish species in the collection occur inshore and can be harvested with traps and spears. Such harvesting accords well with the absence of all fish- hooks and net weights in the Cerro Brujo deposits. If traps and spears were the most common fishing gear employed (Wing and Rubinoff, personal communica- tions), then the techniques employed for getting protein on land and in the sea were probably much the same. It is also important to note the scarcity of birds in our -collection (less than 20 bones; Grayson, personal communication) and the total absence of arboreal reptiles such as iguanas and lizards (Rand, personal communication). CONCLUSIONS For inferring man-induced vegetational changes in the areas around the Cerro Brujo encampment, and reconstructing hunting practices, we can contrast mammalian pairs found in our collection (see Fig. 5). In the tropics, as elsewhere, species of the same family have evolved contrasting morphologies and/or behavior and occupy different ecological niches. Comparing the popularity of related species in the collections is a useful method for inferring past conditions: 1. The white-lipped vs. the collared peccary: The first does not occur (White, personal communication), or occurs in very small numbers (Grayson, 1973), in our collection. The reason for this may be that the white-lipped (although it travels in huge packs) is also more dangerous, especially to hunters without guns, and cannot be caught in traps. Further, a pack needs a large home range and probably a large forest. In contrast, the collared peccary travels in small packs, is more peaceful, needs smaller territories, and is used to living in disturbed conditions. It readily eats cultivated crops. Collared peccaries also do well as semi- domesticates of man. This content downloaded from 132.248.9.8 on Fri, 16 May 2014 11:48:26 AM All use subject to JSTOR Terms and Conditions 346 Linares B G Fig. 5. Most important mammal ter- restrial species at Cerro Brujo. (A) Mazama americana (brocket deer); (B) Dasyprocta punctata (agouti); (C) Cuniculus paca (paca); (D) Dasypus novemcintus (nine-banded armadillo); (E) Tayassu tajacu (collared peccary); (F) Tayassu pecani (white-lipped pec- cary); (G) Odocoileus virginianus (white-tailed deer). Drawings by M. H. Moynihan. F This content downloaded from 132.248.9.8 on Fri, 16 May 2014 11:48:26 AM All use subject to JSTOR Terms and Conditions "Garden Hunting" in the American Tropics 347 2. White-tailed deer vs. the brocket deer: The open brush and grassland species (Odocoileus) was almost seven times more popular at Cerro Brujo than the small, crepuscular, solitary, shy, forest-dwelling brocket deer (Mazama). Because the white-tailed deer can withstand heavy harvesting by man, it was probably one of the few large species that could be hunted near home, in cleared and cultivated fields. 3. The agouti and the paca were hunted in Cerro Brujo in numbers dis- proportionate to their natural biomass (Table IV). As N. Smythe has observed (personal communication), the ratio of one species to the other in our collections (roughly four times as many agoutis as pacas) conforms to their natural densities; the agouti, however, is more diurnal. Smythe's suggestion that the Cerro Brujo inhabitants must have been using snares and traps, which are effective day or night, conforms very well to hunting practices as reconstructed from artifactual evidence. Furthermore, these caviomorph rodents eat all sorts of cultivated plants, including rootcrops and fruits. They live under tree trunks and inside rotten logs (Smythe, 1970). The perfect environment for them is the sort found, for example, in the slashed and mulched fields of the Guaymi of Bocas; because of the constant rains, these fields are burned but infrequently. For additional inferences on hunting practices, we have noted the total absence in our collection of monkeys, sloths, and climbing species (such as squirrels and coatis). The likelihood that the Cerro Brujo group did not use projectile weapons (blowguns, arrows, etc.) with which to fell animals in the higher canopy is increased by the fact that these items are missing in our ex- cavations. But such negative evidence is inconclusive, especially since the hunt- ing gear employed today by a tropical forest group is normally made entirely of perishable materials. As I have previously suggested, the Cerro Brujo people probably origi- nated inland. Two main shifts in hunting were made once these groups migrated to the coast. One was to a small range of terrestrial animals, the other to marine ani- mals. The new terrestrial hunting adaptation that was devised and is represented at Cerro Brujo is what I have called "garden hunting" because in all likelihood it took place in and near cultivated fields and house gardens.7 In this dual sys- tem, animal protein and carbohydrates are spatially concentrated and their Garden hunting is still the predominant form of hunting among many inland South Amer- ican groups, including the Guaymi and Cuna Indians of Panama. The Chiriqui Guaymi until recently pole-fenced their root crops, and built huts in their maize-bean fields, where they stayed overnight to hunt (J. Bort, personal communication). Among the island Cuna, who hunt on the mainland, guarding crops is such an important function of the hunt that a man can freely kill animals in another man's field (Gonzilez, personal communication), while he cannot even touch the other man's crops without complying with elaborate access rules (Howe and Sherzer, 1975). This content downloaded from 132.248.9.8 on Fri, 16 May 2014 11:48:26 AM All use subject to JSTOR Terms and Conditions 348 Linares abundance vis a vis each other is regulated. By reducing seasonality and schedul- ing problems, garden hunting was analogous to, and may have even substituted for, actual animal domestication. ACKNOWLEDGMENTS The Cerro Brujo excavations were financed by a grant from the National Science Foundation (NSF-Gr-2846). Besides myself as principal investigator, a number of colleagues and students participated in the project. Among them I should like to mention Dr. Anthony J. Ra-nere (archeologist), Dr. Philip Young (ethnographer), and Miss E. Jane Rosenthal, Miss Irene Borgono, and Mr. M'aximo Miranda, all graduate students now. Special thanks are owed to Dr. Donald K. Grayson, who did the initial mammalian identifications, and to Mr. Richard S. White, Jr., who reanalyzed the data. Dr. Elizabeth Wing identified the fish, reptiles, and amphibians, and Mr. James West analyzed some of the palyno- logical cores. I should like to thank Wing, White, and West for permission to refer to their unpublished reports. This article has been enriched by the comments of my colleagues at the Smithsonian Tropical Research Institute, namely Drs. Martin H. Moynihan, A. Stanley Rand, Ira Rubinoff, Neal G. Smith, and most specially Nicholas Smythe. Data on the modern Guaymi have been kindly provided by Mr. John Bort and on the San Blas Cuna by the second chief of Niatuppu-Tikantikki, Mr. Gonzalez. REFERENCES Bennett, C. F. (1962). The Bayano Cuna Indians, Panama: An ecological study of liveli- hood and diet. Annals of the Association of American Geographers 52(1): 32-50. Bennett, C. F. (1964). Human Influences on the Zoogeography of Panama. Ibero-Ameri- cana, Vol. 51. University of California Press, Berkeley, 112 pp. Carneiro, R. L. (1964). Shifting cultivation among the Amahuaca of eastern Peru. Volker- kundliche Abhandlungen (Hanover) 1: 9-18. Carneiro, R. L. (1970). Hunting and hunting magic among the Amahuaca of the Peruvian montala. Ethnology IX(4): 3 31-34 1. Coe, M. D., and Flannery, K. V. (1964). Microenvironments and Mesoamerican prehistory. Science 143: 650-654. Colon, F. (1502). Vida del Almirante Don Cistobal Col6n, escrita por su hijo, Hernando Colon (see Lothrop, 1950). Dobyns, H. F. (1966). Estimating aboriginal American population: An appraisal of tech- niques with a New Hemispheric estimate. Current Anthropology 7(4): 395-416. Eisenberg, J. F., and Thorington, R. W. (1973). A preliminary analysis of a neotropical mammal fauna. Biotropica 5(3): 150-161. Gliwi-ez, J. (1973). Characteristics of a population of Proechimys semispinosus (Tomes, 1860) - A rodent species of the tropical rainforest. Bulletin de l'Academie Polonaise des Sciences Cl. 1.XXI-6: 413-418. Goldman, E. A. (1920). Mammals of Panama. Smithsonian Miscellaneous Collections 69(5). This content downloaded from 132.248.9.8 on Fri, 16 May 2014 11:48:26 AM All use subject to JSTOR Terms and Conditions "Garden Hunting" in the American Tropics 349 Gordon, B. L. (1957). Human Geography and Ecology in the Sinu Country of Colombia. Ibero-Americana, Vol. 39. University of California Press, Berkeley, 117 pp. Gordon, B. L. (1961). Notes on the Chiriqui' Lagoon District and adjacent regions of Pan- ama II. Mimeographed report, Department of Geography, University of California, Berkeley, 28 pp. Gordon, B. L. (1969). Anthropogeography and rainforest ecology in Bocas del Toro pro- vince, Panama. Mimeographed report, Department of Geography, University of California, Berkeley, 99 pp. Grayson, D. K. (1973). On the methodology of faunal analysis. American Antiquity 38(4): 432-438. Howe, J. (1974). Village political organization among the San Blas Cuna. Ph.D. disserta- tion, University of Pennsylvania. Xerox, University Microfilms, Ann Arbor, Mich., 442 pp. Howe, J., and Sherzer, J. (1975). Take and tell: A practical classification from the San Blas Cuna. American Ethnologist 2(3): 435-460. Lathrap, D. W. (1968). The "hunting" economics of the tropical forest zone of South America: An attempt at historical perspective. In Lee, R. B., and De Vore, I. (eds.), Man, the Hunter, Aldine, Chicago, pp. 23-29. Lathrap, D. W. (1970). The Upper Amazon. Praeger, New York. Linares, 0. F. (1971). Cerro Brujo, a tiny Guayml hamlet of the past. Bulletin of the Uni- versity of Pennsylvania Museum 13: 27-35. Linares, 0. F. (in press). Adaptive strategies in Western Panama. Paper presented at the Smith- sonian Institution Conference on Biogeographic Approaches to Archeology, May 1974, Washington, D.C. World Archaeology. Linares, 0. F., and Ranere, A. J. (1971). Human adaptations to the tropical forest of wes- tern Panama. Archaeology 24(4): 346-355. Linares, 0. F., Sheets, P., and Rosenthal, E. J. (1975). Prehistoric agriculture in tropical highlands. Science 187: 137-145. Lothrop, S. K. (1950). Archaeology of Southern Veraguas, Panama. Memoirs of the Pea- body Museum of Archaeology and Ethnology, Harvard University, IX(2): 4-7. Mendez, E. (1970). Los Principales Mamiferos Silvestres de Panama. Imprenta Barcenas, Panama City. Meggers, B. J. (1971). Amazonia: Man and Culture in a Counterfeit Paradise. Aldine, Chicago. Morey, R. V. (1970). Ecology and culture change among the Colombian Guahibo. Ph.D. dissertation, University of Pittsburgh. Xerox, University Microfilms, Ann Arbor, Mich. 1973. Murphy, Y., and Murpihy, R. F. (1974). Women of the Forest. Columbia University Press, New York. Nietschmann, B. (1973). Between Land and Water: The Subsistence Ecology of the Miskito Indians, Eastern Nicaragua. Seminar Press, New York. Sauer, C. 0. (1958). Man in the ecology of tropical America. Proceedings of the Ninth Paci- fic Science Congress, 1957, 20: 105-110. Sauer, C. 0. (1966). The Early Spanish Main. University of California Press, Berkeley. Siskind, J. (1973). To Hunt in the Morning. Oxford University Press, New York. Smythe, N. (1970). Ecology and behavior of the agouti (Dasyprocta punctata) and related species on Barro Colorado Island. Ph.D. dissertation, University of Maryland. Walker, E. P. (1968). Mammals of the World, Vols. I and II. Johns Hopkins Press, Baltimore. West, J. (n.d.) Progress report of pollen analysis of core CBII from Cerro Brujo, Bocas del Toro, Panama. Typescript, 3 pp. White, R. (n.d.) Notes on a re-analysis of the Cerro Brujo Fauna. Typescript, 20 pp. Wing, E. (n.d.) Use of aquatic resources at Cerro Brujo (CA-3). Typescript, 9 pp. Young, P. D. (1970). Notes on the ethnohistorical evidence for structural continuity in Guaymf society. Ethnohistory 17(1-2): 11-29. Young, P. D. (1971). Ngawbe: Tradition and Change Among the Modern Guaymi of Wes- tern Panama. University of Illinois Studies in Anthropology, No. 7, Urbana. This content downloaded from 132.248.9.8 on Fri, 16 May 2014 11:48:26 AM All use subject to JSTOR Terms and Conditions