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To cite this article: Simcha Lev-Yadun & Mina Weinstein-Evron (1993) Prehistoric Wood
Remains of Cupressus Sempervirens L. from the Natufian Layers of El-Wad Cave, Mount
Carmel, Israel, Tel Aviv, 20:1, 125-131, DOI: 10.1179/tav.1993.1993.1.125
Article views: 21
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PREHISTORIC WOOD REMAINS OF
CUPRESSUS SEMPERVIRENS L. FROM
THE NATUFIAN LAYERS OF EL-WAD CAVE,
MOUNT CARMEL, ISRAEL
Simcha Lev-Yadun and Mina Weinstein-Evron
ABSTRACT
Introduction
The botanical landscape of Israel has been greatly influenced by human activity
(Zohary 1983), including denudation of large areas (Zohary 1959:338-520) and
both deliberate and unconscious introduction of new plants (Zohary 1962:208-229;
Liphschitz and Waise11974; Dafni and Heller 1990). Since the Middle East was a
major arena for the domestication of many plants (Zohary and Hopf 1988), it is
sometimes difficult to distinguish between local natural plants and adventive plants
that escaped from cultivation, e.g. Ficus sycomorus (Galil, Stein and Horovitz
1976) and Ceratonia siliqua (Liphschitz 1987a; Kislev 1988). The reproductive
biology of Ficus sycomorus indicates that it was probably introduced by man,
although it was suggested that the loss of seed set may be secondary (Galil, Stein
and Horovitz 1976).On the other hand, Ceratonia siliqua seems to be indigenous to
Israel, but its natural distribution was restricted until about two thousand years ago
(Liphschitz 1987a; Kislev 1988). Recently, the question of whether Cupressus
sempervirens belongs to the natural flora of Israel, or is an introduced plant, was
raised, and it was suggested by Liphschitz and Bigger (1989) that this tree was not a
part of the natural forest of Israel in antiquity. In this study we shall present new
evidence to the contrary, indicating that Cupressus sempervirens was part of the
natural forests of Israel, although it was not a common species.
Charcoals 5-10 mm.long were collected from the Early Natufian layer of el-Wad
Cave in Mount Carmel (Fig. 1),dated to ca. 11,000-8,700 B.C.E. (Weinstein-Evron
1991). Samples of cross, tangential and radial longitudinal planes were prepared
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Tel Aviv 20 (1993)
Fig. I. SEM photographs of the wood fragment. I) A cross-section showing four wavy ring
borders (arrows). No resin ducts were found (X 76). 2) A tangential longitudinal section
showing many uniseriate and some biseriate (thick arrows) rays. Radial resin ducts were
not found. The height of rays ranged from one or two cells (small arrows) to 30 cells (X
175). 3) A radial longitudinal section showing the pits between tracheids and ray
parenchyma (X 2630). 4) A radial longitudinal section showing smooth walls of ray
parenchyma cells (X 1750).
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from the charcoals, mounted on metal discs and coated with gold. The samples
were studied under a Jeol JSM 840 A SEM at various magnifications. The plant
material was compared with wood samples of recent trees under both light
microscopy and SEM. Published monographs on xylem anatomy (Greguss 1955;
Fahn, Werker and Baas 1986; Schweingruber 1990) were also used for anatomical
comparison.
Results
One of the samples, EW -89 G-40-C, 172, was of a conifer. The wood was
composed of tracheids, and four growth rings were seen in the cross-section (Fig.
1:1). No resin ducts were found, and the ring border was somewhat wavy, a
common shape for the ring border in Cupressus sempervirens. The curvature of the
growth rings was small, indicating that the charcoal came from a mature tree.
Another indication of its origin from a mature specimen was the occurrence of
biseriate rays (Fig. 1:2), which, in conifers, appear in mature wood. The pit pairs in
the rays were small (Cupressoid) (Fig. 1:3) and not window-like (Pinoid) (IAWA
Committee on Nomenclature 1964:38). Mean ray height was 8.4 cells, and ranged
from 1-30 cells (Fig. 1:2). The end walls of the ray parenchyma cells were smooth
(Fig. 1:4).
Discussion
This is the first record of conifer wood remains from a prehistoric Mount Carmel
site. The early date indicates that this wood was local, and not imported. The lack of
several diagnostic anatomical structures: resin ducts, tracheids in the rays, window-
like pit pairs in the rays and fringed torus margins excluded both Pinus and Cedrus
as well as all other members of the Pinaceae that grow in the Eastern Mediterranean
region (see Greguss 1955; Fahn, Werker and Baas 1986; Schweingruber 1990). The
distinction between Juniperus and Cupressus was based on two criteria: ray height
and indentures of ray parenchyma end walls (Greguss 1955; Fahn, Werker and
Baas 1986:55-56; Schweingruber 1990:135-147). The differences in the two
characteristics were very clear when fresh wood of mature Cupressus sempervirens
was compared with that of Juniperus phoenicea. The wood was thus defined as the
trunk-wood of Cupressus sempervirens.
Members of the genus Cupressus do not form extensive forests as do members of
the genus Pinus. American species of the genus Cupressus usually grow in small
populations (Wolf 1948). Wolf suggested that. Cupressus is not sufficiently
aggressiveto colonize new territories since seed production and methods of dispersal
are such that there is practically no possibility of reaching nearby suitable areas.
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Lev-Yadun and Weinstein-Evron: Prehistoric Wood Remains
Acknowledgments
We thank Prof. Amots Dafni, Dr. Ella Werker and Dr. Daniel Kaufman for their
comments on the manuscript, and Mr. Felix Skandarani for his help with the SEM
work. This study was supported by the Irene Levi Sala Care Archaeological
Foundation, The Nature Reserves Authority of Israel and The Faculty of
Humanities, University of Haifa.
REFERENCES
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