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72<br />

ANA LUISA ANAYA<br />

allelopathy is a challenging and exigent matter of study. At present we have proof<br />

that secondary metabolites are involved with biotic interactions, and that allelopathic<br />

effects may restrict or enhance, alone or in relation with other environmental factors<br />

(light, temperature, humidity and nutrients), the distribution, health and growth of<br />

species in natural, artificial or managed communities. In the search for application of<br />

allelopathy knowledge is crucial to understand other biotic interactions (competition,<br />

defense against herbivory) and also the actual and full significance of a mixture of<br />

secondary metabolites all together acting in the environment (Anaya, 1999).<br />

Allelopathy typically operates through the release, modification, and joint action<br />

of a number of allelochemicals in a particular situation, and transitions through the<br />

soil add to the complications for explaining the phenomenon. The frontiers in research<br />

on allelopathy include isolation of additional compounds that may be involved, and<br />

determining more precisely how allelochemicals production is regulated and how the<br />

compounds function to inhibit growth. Such information may allow modification of<br />

crop plants so they have enhanced capability for weed suppression. Alternatively,<br />

new herbicides, pesticides, and growth regulators may be developed from some of<br />

plant and microorganisms compounds (Einhellig, 1989).<br />

In the study of biological interactions mediated by secondary metabolites it is<br />

very important to perform multidisciplinary investigations in a long term approach in<br />

order to understand these interactions from an holistic point of view and make use of<br />

them for beneficial purposes in the management of natural resources in agroecosystems.<br />

8. REFERENCE<br />

Abrahim, D., Braguini, W.L., Kelmer-Bracht, A.M., Ishii-Iwamoto, E.L. Effects of four monoterpenes on<br />

germination, primary root growth, and mitochondrial respiration of maize. J Chem Ecol 2000; 26:611-<br />

624.<br />

Ahonsi, M.O., Berner, D.K. Emechebe, A.M., Lagoke, S.T. Selection of rhizobacterial strains for suppression of<br />

germination of Striga hermonthica (Del.) Benth. Seeds. Biol Con 2002; 24:143-152.<br />

Anaya, A.L., S. del Amo. Allelopathic potential of Ambrosia cumanensis H.B.K. (Compositae) in a tropical<br />

zone of México. J Chem Ecol 1978; 4:289-304.<br />

Anaya, A.L., Ramos, L., Cruz, R., Hernández, J., Nava, V. Allelopathy in Mexican Traditional Agroecosystems:<br />

A case study in Tlaxcala. J Chem Ecol 1987; 13:2083-2101.<br />

Anaya, A.L., Hernández-Bautista, B.E., Torres-Barragán, A., León-Cantero, J. Jiménez-Estrada, M. Phytotoxicity<br />

of cacalol and some derivatives obtained from the roots of Psacalium decompositum (A. Gray) H. Rob &<br />

Brettell (Asteraceae), “matarique” or “maturín”. J Chem Ecol 1996; 22:393-403.<br />

Anaya, A.L., Pelayo-Benavides, H.R. Allelopathic potential of Mirabilis jalapa L. (Nyctaginaceae): Effects on<br />

germination, growth and cell division of some plants. Allelopathy J 1997; 4:57-68.<br />

Anaya, A.L. Allelopathy as a Tool in the Management of Biotic Resources in Agroecosystems. Crit Rev Plant<br />

Sci 1999; 18: 697-739.<br />

Anaya, A.L., Mata, R., Sims, J., González-Coloma, A., Cruz-Ortega, R., Guadaño, A., Hernández-Bautista<br />

B.E., Ríos, G., Gómez-Pompa, A. Allelochemical potential of Callicarpa acuminata (Verbenaceae). J<br />

Chem Ecol 2003; 29:2725-2740.<br />

Bais, H.P., Walker, T.S., Stermitz, F.R., Hufbauer, R.A., Vivanco, J.M. 2002. Enantiomeric-dependent phytotoxic<br />

and antimicrobial activity of (±)-catechin. A rhizosecreted racemic mixture from spotted knapweed. Plant<br />

Physiol 2003; 128: 1173-1179.<br />

Barazani, O. Friedman J. Allelopathic bacteria and their impact on higher plants. Crit Rev Microbiol 2001;<br />

27:41-55.

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