Establishment of an agroforestry research network in Victoria,Australia (1983–85)

From 1983 to 1985, a network of agroforestry research trials was established at six localities throughout Victoria. This paper describes experimental designs and establishment procedures used at the trial sites. The overall aim of the research program is to provide definitive information on the costs and benefits of a wide range of agroforestry combinations. Accordingly, trials were established at the following locations to test a total of 93 tree species grown in combination with specific types of agriculture:

1. Carngham (near Ballarat) — sheep grazing andPinus radiata D. Don (radiata pine);
2. Hamilton (several sites) — sheep grazing and mixed tree species;
3. Kyabram — irrigated pastures andEucalyptus grandis W. Hill ex Maiden (flooded gum);
4. Rutherglen — cereal cropping and shelterbelts;
5. Myrtleford — irrigatedMentha spp. (mint) and two clones ofPopulus spp. (poplar); and
6. Neerim South (near Warragul) — cattle grazing and mixed tree species.

Conventional and systematic experimental designs have been used in setting up these trials, which in total constitute the most comprehensive agroforestry research in Australia. This paper describes these trials in detail, and stresses the importance of their continued expert management, so that the full benefits of the work can be realised for rural Victoria.     

Changes through time in traits of poplar clones in selection trials

Growth, survival, stem characteristics, resistance to wind, and canker disease of 51 poplar clones were evaluated at age 9 and 10 years, and compared to measurements at age 3 in two trials on the Lower Valley of the Colorado River, Argentina. About 30% of the clones in both trials had large changes in growth rankings at age 9 and 10 compared to rankings at age 3. Canker incidence increased about 4-fold between age 3, and measurements at age 9 and 10. Stem form was in general satisfactory, and wind incidence was almost nil. In trial 1, clones 588–1, Conti 12, 582–41, and 582–5 occupied the upper positions in the growth rankings at age 3 and 10, and the clone 588–1 ranked first both in growth and canker incidence in 1998. Stem growth trajectories of clones with similar growth rates did not differ among clones with, and without canker disease. In trial 2, the range in growth among clones was narrower than in trial 1, and canker disease, although of minor incidence, was present in most clones at age 9. Some of the P. deltoides clones in the trials had similar growth, and less canker disease than the Euroamerican clones commonly grown in the region, but progressive canker incidence should be addressed with additional selection trials.     

Peptidases of Trichobilharzia regenti (Schistosomatidae) and its molluscan host Radix peregra S. Lat. (Lymnaeidae): construction and screening of cDNA library from intramolluscan stages of the parasite

Trichobilharzia regenti is a neurotropic bird schistosome,causing cercarial dermatitis in humans. In this study, ZAP cDNA expression library from Radix peregra s. lat. hepatopancreases containing intramolluscan stages of T. regenti was constructed and screened using PCR with specific and degenerate primers, designed according to previously described serine and cysteine peptidases of other parasite species. Full-length sequences of cathepsins B1 and L, and two serine peptidases, named RpSP1 and RpSP2, were obtained.The protein-protein BLAST analysis and parallel control reactions with template from hepatopancreases of T. regenti non-infected snails revealed that only cathepsin B1 was of parasite origin. The remaining sequences were derived from the snail intermediate host, which implies that the initial source of parasite mRNA was contaminated by snail tissue.Regardless of this contamination, the cDNA library remains an excellent molecular tool for detection and identification of bioactive molecules in T. regenti cercariae.     

Plants,small mammals,and the hierarchical landscape classifications of Patagonia

Assemblages of plants were studied at 14 sites in northern Patagonia corresponding to localities at which we (Monjeau et al. 1997) earlier studied the relationship between small mammal assemblages and landscape classifications. This allowed us to test predictions that both plants and small mammals correspond to the more inclusive hierarchical landscape divisions but that plants track better than small mammals the less inclusive divisions. Species presence or absence of plants at each locality was used in a series of multivariate analyses and compared by correlation analysis with those generated from small mammal species data. Assemblages of both plants and small mammals corresponded to the upper divisions, which are based on climatic and geomorphological features, but small mammal assemblages did not correspond to the lower divisions of the landscape classifications. Three factors are considered as explanations for the observed differences between plants and small mammals: a) small mammal habitat is determined more by plant growth form than by plant species; b) trophic level differences between the two groups; and c) species pool size affects the resolution of microhabitat correspondence. Our data indicate that both plant assemblages and small mammal assemblages respond to climatic and geomorphological features, which is in contrast to the paradigm that mammal assemblages simply follow plant assemblages. We also attempted to reconcile classification systems in Patagonia by proposing a nomenclatural system based on a hierarchical classification. In the system proposed, ecoregion is the lowest division small mammal assemblages can recognize in Patagonia. Finally, we conclude that the hierarchical nature of landscapes based on a holistic view of environments reflects real entities that are not just the perceptions of landscape ecologists.     

Age determination of large live trees with inner cavities: radiocarbon dating of Platland tree,a giant African baobab

• Introduction   

For large trees without a continuous sequence of growth rings in their trunk, such as the African baobab (Adansonia digitata L.), the only accurate method for age determination is radiocarbon dating. As of today, this method was limited to dating samples collected from the remains of dead specimens.