and that resources were exploited from a widevariety of habitats, including the coast and themountains. Fifteen species of aquatic plants fromfreshwater marshes of the distant Maullín flood- plain and from coastal dunes and brackish water estuaries of the delta, along with gomphothere(
Cuvieronicus sensu
Casamiquela) and paleo-camelid (
Paleolama
sp.) meat, wild potatoes(
Solanum maglia
), and 45 other plant speciesfrom inland forests and wetlands provided the bulk of the Monte Verdeans
’
diet (
12
,
13
). In-cluded in the plant inventory were four previ-ously reported varieties of seaweed,
Durvillaea Antarctica
(
cochayuyo
),
Porphyra
sp. (
luche
),
Gracilaria
sp. (
pelillo
), and
Sargassum
sp.,from sandy and rocky shorelines (
14
–
16
). Allof these species are edible and have important medicinal properties. Also recovered were theremains of 19 other probable medicinal spe-cies, 5 of which came from coastal environments(
14
–
16
). Other coastal resources collected from beaches and transported to the site were dis-coidal pebbles made into stone tools, bitumenused as adhesive to attach tools to wooden shafts,and marine fossils (
12
,
13
).Our new analyses are from 27.2 liters of previously excavated but unstudied sediment fillfrom 24 hearths and braziers in the floors of twostructures thought to be the remains of a medic-inal hut and a residential tent. We recovered theremains of seaweed and other economically im- portant plants (SOM text, section 2, and table
S
1) and three stones, one of which is a flaketool. Identified were
Porphyra
sp. and
Durvillaea Antarctica
(Fig. 2) and five new species of sea-weed:
Gigartina
sp. (
luga roja
);
Mazzaella
sp.(
luga cuchara
);
Porphyra columbina
; probably
Sarcothalia crispata
(
luga negra
, Fig. 3); and
Macrocystis pyrifera
(
huiro
) (
13
). We also recov-ered
Trentepohlia
sp., an algae that is availableexclusively on trees (
Aextoxicon punctatum
and
Griselinia jodinifolia
) and rocks in the littoralzone. The excellent preservation of the speci-mens allowed species-level identifications basedon cellular structure, plant morphology, and color.Two accelerator mass spectrometry radiocarbondates derived from fragments of
Gigartina
sp.on the floor of a wishbone-shaped hut and from
Mazzaella
sp. in a brazier on a tent floor are re-spectively between 14,190 and 13,990 cal yr B.P.(~12,290 ± 60 C
14
yr B.P., Beta Analytic radio-carbon dating service sample number 238355)and 14,220 and 13,980 cal yr B.P. (~12,310 ±40 C
14
B.P., Beta Analytic sample number 239650). These dates agree with those derivedfrom wood artifacts and charcoal in hearths at Monte Verde II, which range between 14,600and 14,200 cal yr B.P. (
13
).It was difficult to count the soft remains of the 10 species of algae because many were frag-mented and mixed with other plants in masti-cated cuds, thought to be representative of anancient pharmacopeia (
14
,
15
) (SOM text, sec-tion 3, and fig. S1), or were trampled and em- bedded in hut floors. However, the dry weight total of all excavated seaweed remains was~125 g. Several algae fragments were partially burned, suggesting that they had been dried, probably for transport from the coast or for storage, or were cooked. The fragility of soft leafyseaweeds, their unlikely preservation in archaeo-logical sites, and yet their widespread dispersionin hearths and braziers across the site and their combination with other medicinal plants in theform of masticated cuds suggest their value for both food and medicinal purposes.The seaweeds represent contrasts in en-vironment and seasonal availability. Four genera (
Durvillaea
,
Porphyra
,
Mazzaella
, and
Sarco-thalia
) derive from rocky coastlines and inter-tidal pools located west and south of MonteVerde (
16
,
17
), whereas three (
Gracilaria
,
Gig-artina
, and
Macrocystis
) originate only fromsandy coastlines west of the site. The peak avail-ability of three (
Mazzaella
,
Gigartina
, and
Sarco-thalia
) occurs from early spring to early summer,one (
Gracilaria
) is available from late springto early summer, one (
Porphyra
) is found in mid-summer, and one (
Durvillaea
) occurs in late sum-mer to early fall (
18
–
21
).
Sargassum
sp. (Fig. 4)is a warm-water species with a wide Pacific nat-ural range. Its growth anywhere in Chile, wherethe cold Humboldt Current sweeps the coast, isdoubtful (
17
–
22
).
Sargassum
probably reachedChile through violent storms or major El Niñoevents, or perhaps the configuration of oceancurrents was different at the time of site occu- pation.
Trentepohlia
sp. is available year roundalong the littoral. Seaweed collection by MonteVerdeans was thus conducted at various coastallocales from early spring to early fall. Today, thetidal range of the sea varies from 6.5 m near Puerto Montt in the Reloncavi Bay to 4 m at the mouth of the Maullín River, in both areas producing a wide and abundantly availableresource-rich intertidal beach. With the excep-tion of
Sargassum
sp., moderate quantities of all varieties of seaweeds are deposited alongthe shoreline during storm surges. All nine sea-weed species recovered at Monte Verde II areexcellent sources of iodine, iron, zinc, protein,hormones, and a wide range of trace elements, particularly cobalt, copper, boron, and manga-nese (
23
–
29
). Secondary beneficial effects of these seaweeds include aiding cholesterol me-tabolism, increasing the calcium uptake of bones,antibiotic effects, and increasing the body
’
s abil-ity to fight infection. These species have medic-inal uses that closely correspond to commoncontemporary health problems in the study area today (SOM text, section 3). Two species,
Gig-artina
and
Sargassum
, are non-edible and wereevidently used exclusively for medicinal pur- poses. Collectively, the seaweeds and 10 other plant species at Monte Verde II suggest a medic-inal stock derived from the cool temperate en-vironment of the region. These same species areused today as medicinal plants by local indig-enous populations.We also recovered a total of 268 edibleseeds, fruits, and other plant parts (SOM andtable S1) from the processed feature fills, whichcorrespond with the genera previously reported
Fig. 2.
Microscopic view of an archaeologicalspecimen of
Durvillaea antarctica
from a hearthmatrix located in the remains of a domestic hut.Scale bar, ~100
m
m.
Fig. 3.
Microscopic view of an archaeologicalspecimen of
Sarcothalia crispata
from a hearthmatrix located in the remains of a domestic hut.Scale bar, ~ 200
m
m.
Fig. 4.
Microscopic view of
Sargassum
sp. from the floorof the wishbone-shaped hut.Scale bar, ~100
m
m.
www.sciencemag.org
SCIENCE
VOL 320 9 MAY 2008
785
REPORTS
Add a Comment