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Archaeological sites on the west coast for evaluating the disposition and vul-
of Mexico provide long-term records nerability of these endangered species
of human predation on sea turtle pop- today (Limpus 1995; Spotila 2004).
ulations. These large reptiles, valuable Sea turtles occupy most of the
for their meat, eggs, shell, oil, and world’s tropical and subtropical oceans
skin, are easily obtained from nesting with five species—Dermochelys cori-
beaches, but prolonged predation can acea [Leatherback], Eretmochelys im-
disrupt rookeries and lead to population bricata squamata [The Pacific Hawks-
fragmentation and local extirpation. Our bill], Caretta caretta gigas [Pacific Log-
recent excavations at two sites in coastal gerhead], Lepidochelys olivacea [Olive
Guerrero near Acapulco indicate that Ridley], Chelonia mydas agassizi [East
people hunted sea turtles, most likely Pacific Green Turtle]—present along
from nesting grounds, by at least 5500 Mexico’s Pacific Coast (Cliffton et al.
cal yrs BP and significantly reduced their 1995). These resilient animals have per-
local availability within a 3,000 year sisted on the planet for over 100 million
period. These data help provide a deeper years, surviving the Cretaceous-Tertiary
historical and environmental framework extinction event about 65 mya, but
231
Carley B. Smith et al.
have witnessed dramatic declines in ing beaches are known from Michoa-
their numbers worldwide in the last 100 can, Guerrero, and Oaxaca, with the
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Figure 1. Map showing modern turtle rookeries on the Pacific Coast of Mexico. Inset shows
archaeological sites in the Acapulco region. 1 = Puerto Marqués, 2 = La Zanja, 3 =
Arroyo Seco, 4 = El Recreativo, 5 = Barrio Nuevo, 6 = La Sabana, 7 = Infonivit, 8 = La
Picuda, 9 = Palma Sola, 10 = Hornos, 11 = Tambuco.
this historical information and provide These records contain evidence for the
greater time depth to study the dynamic transition to maize-based food produc-
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Figure 2. Graph showing decrease in sea turtle remains (NISP) over time at Puerto Marqués and La
Zanja. Numbers have been volumetrically corrected (per m3 ) for comparative purposes
(see Table 1 caption for volumetric information).
Table 1. Identified sea turtle remains in NISP and MNI from Puerto Marqués and La Zanja.
Not corrected for volume. Volumes excavated from Puerto Marqués are 1.6 m3 (Late
Archaic), 2.4 m3 (Early Formative), 3.6 m3 (Middle Formative), and 0.39 m3 (Late
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Formative). Volumes excavated for La Zanja are 2.4 m3 (Early Formative) and 3.2
m3 (Middle Formative).
LATE FORMATIVE
Puerto Marqués
Green Chelonia mydas 7 2 1 1 2 1 0 0
Hawksbill cf. Eretmochelys 1 1 0 0 0 0 0 0
imbricata
Sea Turtles Cheloniidae 234 21 12 0
La Zanja
Loggerhead Caretta caretta 2 1 1 1
Green Chelonia mydas 8 2 21 5
Olive Ridley cf. Lepidochelys 2 1 0 0
olivacea
Sea Turtles Cheloniidae 497 192
1). Sea turtle bone frequencies at Puerto declines are evident in both records.
Marqués decline from the Late Archaic We interpret this trend as disturbance
through Middle Formative (∼2800–2500 to nesting grounds in the immediate
cal yrs BP) and disappear entirely from vicinity of these prehistoric villages.
all later levels. A similar trend is visible in Although industrial scale hunting has
the stratigraphic record at La Zanja. Taxa severely impacted sea turtle populations
identified at this more interior location in recent years, prehistoric hunting and
include C. mydas, C. caretta, and L. disruption of breeding colonies is par-
olivacea. The number of sea turtle bones tially responsible for shaping the mod-
is highest (n = 212) in the Early For- ern distribution and extent of these pop-
mative period (∼3400–3100 cal yrs BP) ulations. For instance, our data suggest
deposits and a declining trend is evident that Green sea turtle nesting beaches
based on reduced numbers of bones in extended farther to the south than
the Middle Formative (2800–2500 cal yrs those recorded historically in coastal
BP) assemblage. Michoacan, at least prior to disruptions
Our work in coastal Guerrero sug- associated with expanding prehistoric
gests a reduction in the availability of sea populations in the Late Holocene. Olive
turtles that parallels expanding human Ridley (L. olivacea) remains in the
populations in the region (see Figure Early Formative period deposits at La
1, inset). Sea turtle bones and carapace Zanja are also suggestive of nesting
fragments were the most common rep- areas closer than those recorded his-
tile remains in the earliest deposits at torically at Piedra de Tlacoyunque and
the two locations sampled. Subsequent Chacahua.
spanning the Holocene will help This work was funded by the National
elucidate the biogeographical distribu- Science Foundation (BCS-0211215).
tions of the different sea turtle species
along the Pacific Coast of Mexico. How- REFERENCES
ever, our preliminary work shows that
the distribution of Green sea, and pos- Cliffton, K., D. O. Cornejo, and R. S. Felger. 1995.
sibly Olive Ridley, turtles, was greater Sea turtles of the Pacific Coast of Mexico. In
than that recorded historically, an impor- Biology and Conservation of Sea Turtles, rev.
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Spotila, J. R. 2004. Sea Turtles: A Complete Guide
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