The breeding system of Ramosmania heterophylla–dioecy or heterostyly?

OWENS, S.J., JACKSON, A., MAUNDER, M., RUDALL, P.JOHNSON, M.A.T., 1993. The breeding system of Ramosmania heterophylla– dioecy or heterostyly?Ramosmania heterophylla (Cafe Marron), endemic to Rodrigues, Mauritius, is now almost extinct, since it appears to exist in the wild as a single plant, but has recently been successfully established at Kew by means of vegetative cuttings. Despite plenty of flowers on the Kew plants, attempts to set seed by manual pollination for seed banking purposes have failed. This investigation showed that pollen is viable and that embryo sacs appear fully developed. Lack of seed set is a result of the non-functional stigmas on short styles. The most likely explanation is that the last-known plant is male, although heterostyly or a mutant stylar developmental gene cannot be ruled out. The plant has a chromosome number of 2n= 22.     

Randomly Amplified Polymorphic DNA (RAPD) and Isoenzyme Analysis of Trypanosoma rangeli Strains

ABSTRACT. Sixteen Trypanosoma rangeli strains were compared by isoenzyme and randomly amplified polymorphic DNA (RAPD) analysis. Eight strains were isolated from either Rhodnius prolixus or Homo sapiens from Honduras, Colombia and Venezuela. Another eight strains were isolated from either Panstrongylus megistus or the rodent Echimys dasythrix from the State of Santa Catarina, southern Brazil. All six T. rangeli strains isolated from P. megistus were co-infections with Trypanosoma cruzi , demonstrating an overlap of the sylvatic cycles of these parasites and that the accurate identification of species is of utmost importance. Both isoenzyme and RAPD analysis revealed two distinct groups of T. rangeli strains, one formed by the strains from Santa Catarina and the other, by the strains from Honduras, Colombia and Venezuela. With the five enzymes used, all the strains from Santa Catarina had identical profiles which overlapped with those of the other regions only in the pattern obtained with malic enzyme. Analysis of 138 RAPD bands by means of an unweighted pair group method analysis (UPGMA) phenogram using the Dice similarity coefficient allowed the separation of the two groups based on their divergence at a lower level of similarity than the phenon line. We show that the identification of T. cruzi and T. rangeli in naturally mixed infections is readily achieved by either RAPD or isoenzyme analysis.