Usually lizards are considered to be insect
eating. But in
desert areas, the extreme climatic conditions and the fluctuating amount
of food often result in interesting adaptations and relations between
plants and animals, and their environment. The following is a report on
one such case involving flower predation by lizards.
On the
14th
November, 1973, we were camped on the few hundred metres wide coastal
plain at Paposo (Lat. 25°05‘ South, Long. 70°30‘, approx.), which
lies between the sea and the steeply rising coastal mountain range in the
Atacama desert, Chile. Because of the extremely interesting vegetation at
Paposo, various writers have published further information, such as
Philippi (1860), Reiche (1907),
Johnston
(1929), Kummerow (1961), Follmann & Weisser (1966) and Rundel & Mahu
(1975). This coastal plain is inhabited mainly by a dense population
of the cactus
Copiapoa
haseltoniana
of which
the cylindrical stems are generally oriented northwards (Mooney et. al.
(1975), see figure 1).

Fig. 1.
Copiapoa haseltoniana
Backeberg in its habitat at Papaso. The ochre wool of the pad
distinguishes this species from
Copiapo cinerea
(Phil.) Backeberg. The yellow flowers are not only visited by insects,
but also predated by lizards, probably
Lio/aemus p/atei platei.
The lizard can be seen on the upper right plant head.
As is
common in areas such as this, with coastal desert climate, the early
morning was overcast. By the middle of the morning however, the cloud
cover had begun to dissipate, with the sun breaking through the gaps
warming the ground below. Stimulated by the warmer temperatures and/or
light, the lizards came out of their hiding-places, and could be seen
perching on rocks where they warmed themselves in the sun‘s rays. Now
insect life was also more active, with many wild bees, ants, and flies
paying visits to the bright yellow flowers of the
Copiapoa
haseltoniana
plants.
The
lizards, which appeared to be Liolaemus platei platei, Ortiz
(1975), soon began to visit the C. haseltoniana plants, moving
agilely in between the rows of spines on the ribs. When the first lizard
approached a flower of C. haseltoniana it was expected that it
would remain there and prey on visiting insects. Much to our surprise, the
lizard moved right onto the flower and began eating parts of it,
especially the pollen laden stamens (Fig. 2). This preference could be
related to a possible high nutrient (proteins?) content of the pollen. We
observed the lizards repeatedly, and at no stage did they attempt to catch
any of the insects that passed close by them.

Fig. 2. The herbivorous lizard on the
C. haseltoniana
flower. They seem to prefer to eat the stamens, but occasionally they
also grasp a petal such as can be seen in the photograph. The lizard
has a petal in its mouth. An ant can be seen at the base of the flower.
While we watched, no attempt was made by the lizard to take this ant or
any other visiting insects.
Considering the large quantity of seed still produced, together with the
low germination and establishment rate that
Copiapoa
haseltoniana
normally
exhibits in its natural environment, the overall impact of the predation
of flowers by cf. Liolaemus platei plaitei on the population of
Copiapoa haseltoniana
is
probably low.
Herbivory by lizards has been
reported to take place in other deserts, in montane areas and higher
latitudes in Chile, as well as under laboratory conditions. Liolaemus
nigromaculatus has
been observed eating flower buds at the localities Los Molles and Zapallar
in Central Chile (F.R. Fuentes (1975)). Nevertheless, this is, to our
knowledge, the first time that flower predation by lizards is reported
from the Atacama Desert, and it is probable that it is a much more common
phenomenon than is at present realized. Another animal which we observed
feeding on flowers of C. haseltoniana were goats, which (in spite of the
protection by the spine barrier) were able to successfully remove complete
flowers with their tongues. The shiny black seeds are harvested by ants
and sometimes the fruits are completely emptied by them. (See also Weisser
(1973) and Speta (1967)).
Summary
Flower
predation by lizards,
Liolaemus plalei platei
(lguanidae),
on Copiapoa
haseltoniana
(Cactaceae)
is
reported from the locality of Paposo, Atacama Desert, Chile.
Acknowledgements
We wish to
acknowledge the support received from the Facultad de Ciencias, Universidad
de Chile, Santiago, from the Botanical Research Institute,
Pretoria,
and to our travelling companions Prof. H. Mooney and Mrs S. Gulmon. For
their valuable suggestions we want to thank Dr F.R. Fuentes, Prof. J.C.
Ortiz, and Mr T. Arnold.
References
Backeberg, C. (1970). Das Kakteenlexikon. Ed. G. Fischer Verlag, Jena.
Donoso Barros, R. (1966). Reptiles de Chile. Ed. Universidad de
Chile, Santiago (in Ortiz 1973)).
Follmann, G., & Weisser, P.J. (1966). Oasis de neblina en eI Norte de
Chile. Bol. Univ. de Chile 67:34—38.
Fuentes,
F. R. (1975). Personal communication.
Johnston,
I.M. (1929). The coastal flora of the Departments of Chañaral and
Taltal. Contr. Gray Herb. 85:1—1 80.
Kummerow,
J. (1961).
Nebelpflanzen am Rande der Wüste Atacama. Kosmos 7:319—323.
Mooney, H.A., P.J. Weisser & S.L. Gulmon (1975).
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Copiapoa
haseltoniana.
Unpublished
manuscript.
Ortiz, J.C. (1973). Nota distributional sobre Liolaemus platei
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Ortiz, J.C. (1975).
Personal
communication. Philippi, R.A. (1860).
Viaje al desierto de
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I-IV: l-236.
Rundel.
P.W. & M. Mahu (1975). Community
Structure
and Diversity in a Coastal Fog Desert in Northern Chile.
Unpublished manuscript.
Reiche. K. (1907). Grundzüge der Pflanzenverbreitung in Chile. In:
Engler, A. & Drude O. Die Vegetation der Erde VIII: I —374.
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Speta, F. (1967). Möglichkeiten der Samenverbreitung bei Cactaceen mit
besonderer Berücksichtigung der Myrmekochorie.
Kakt. u. a. Sukk.
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Weisser, P.J. (1973). Morfologia externa de las semillas de algunas
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Botanical Research
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Pretoria
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