Daemonorops verticillaris (Griff.) Mart. and D. macrophylla Becc. are two rattan palms of peninsular Malaysia which are characteristically associated with a resident ant colony. The ants construct a nest utilizing plant hairs alone, or hair and spines, which is capable of absorbing approximately 185 percent water by weight. Use of a 14C tracer shows that wateror nutrient-enhanced throughfall is absorbed by the nest, subsequently taken into the plant, and translocated to developing tissues. D. verticillaris and, to a lesser extent, D. macrophylla trap falling debris (leaves, twigs, and fruits) around the plant apex. Precipitation, or throughfall, percolates through this material, is directed toward the stem, and is absorbed by the ant nest material. Taken together, debris collection and water absorption constitute a unique and effective mechanism of nutrient enhancement and recycling for these particular plants. NUTRIENT ACQUISITION IS A PRIME REQUISITE for any organism's continued existence. In addition to maximizing purely physiological functions, tissue nutrient level can also affect the production and growth of anatomical characteristics. Most plants seem to exist at a level somewhat below maximal growth in that added nutrients increase growth over wild populations. Methods for nutrient acquisition should have been under intense selection pressure throughout a species' evolutionary history, and to this end, we find that a variety of characteristics, both physiological and morphological, aid in nutrient trapping, uptake, and incorporation. Lamont (1982) has reviewed nutrient uptake in plants, and his list of modifications includes: mycorrhizal associations; nitrogen fixation; carnivorous habit; proteoid, capillaroid, and dauciform root systems; persistent, detritis trapping leaf bases which include aerial roots; and a parasitic habit. To this list we would add direct nutrient uptake by leaves (Benzing et al. 1976, Bentley & Carpenter 1984) and certain ant-plant relationships in which there is an uptake of nutrients by the plant from various ant residues. We know of such uptake in Hydnophytum (Rubiaceae) (Huxley 1978, Rickson 1979), several Bromeliaceae (Benzing 1970), and Cecropia (Moraceae), Macaranga (Euphorbiaceae), and Piper (Piperaceae) (F. R. Rickson, pers. comm.). No long term exclusion studies have explored any actual benefit of this uptake to the plant; however, over the past four years a trend toward lower flower production and seed set in a set of greenhouse Hydnophytum plants from which fertilizer has been withheld is beginning to be discernable (F. R. Rickson, pers. comm.). In addition, a number of studies have shown increased plant fecundity associated with insect trapping (Darwin 1878, Kellermann & Von Raumer 1878, Harder & Zemlin 1967). Twelve genera and 600 species of rattans grow in South East Asia. Ants are consistently associated with 5 species in 2 genera. Daemonorops macrophylla and D. verticillaris are two rattan palms of the lowland dipterocarp forests of western peninsular Malaysia. Rattans are climbers, and Daemonorops uses a modified leaf rachis tip possessing recurved spines to anchor the leaves as the stem ascends into the forest canopy. These two species are constantly associated with an ant colony living on the leaf sheaths; D. verticillaris especially, by virtue of leaf placement and spine orientation, accumulates dead leaves and other debris in the region of the shoot apex. Rattans possess a leaf sheath that bears spines (Fig. 1A). The spines may be small but most often are large, stiff, and formidable to the collector. Spines in herbarium material are oriented horizontally or downward in most species; however, in the two species considered here, particularly D. verticillaris, many of the spines point decidedly upward, and a few inserted at the junction of the petiole and sheath reach 10 cm in length. It is the upward orientation of spines and new leaves which allows for the collection of debris. Field observation indicated that the ant colony nest material was very absorbent of rainwater and throughfall. This fact, coupled with the cluster of debris around the shoot apex, suggested that the total system might function in nutrient acquisition and transfer to the main plant stem. I Received 28 January 1986, revision accepted 23 August 1986. BIOTROPICA 18(4): 337-343 1986 337 This content downloaded from 157.55.39.58 on Tue, 15 Nov 2016 03:54:50 UTC All use subject to http://about.jstor.org/terms FIGURE 1. Morphology of D. verticillaris and D. macrophylla. (A) General morphology of D. verticillaris. (B) Section through the center of a stem as in Figure IA. Note the overlapping spines and the indumentum material placed within the resulting cavity. 338 Rickson and Rickson This content downloaded from 157.55.39.58 on Tue, 15 Nov 2016 03:54:50 UTC All use subject to http://about.jstor.org/terms STUDY SITE AND METHODS The study was conducted at Pasoh Forest Reserve, Negri Sembilan, Malaysia, between October 1981 and March 1982. Pasoh is an IBP study area located approximately 2?59'N latitude and 102?17.5'E longitude. The area is classified as a lowland dipterocarp forest and receives an annual rainfall of approximately 200 cm (Manokaran
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