Climate warming and the rainforest birds of the Australian Wet Tropics: Using abundance data as a sensitive predictor of change in total population size

Global average surface temperatures have increased rapidly over the last 100 years and there is accumulating evidence that climate change is already causing shifts in species’ distributions. We use extensive abundance data and expected range shifts across altitudinal gradients to predict changes in total population size of rainforest birds of Australian tropical rainforests in response to climate warming. According to our most conservative model scenario, 74% of rainforest birds of north-eastern Australia are predicted to become threatened (including 26 critically endangered species) as a result of projected mid-range warming expected within the next 100 years. Extinction risk varies according to where along the altitudinal gradient a species is currently most abundant. Upland birds are most affected and are likely to be immediately threatened by even small increases in temperature. In contrast, there is a capacity for the population size of lowland species to increase, at least in the short term. We conclude that abundance data collected across climatic gradients will be fundamental to gaining an understanding of population size change associated with climate warming.     

Within-stand and seasonal variations of specific leaf area in a clonal Eucalyptus plantation in the Republic of Congo

Specific leaf area (SLA; m²_leaf kg^?1_leaf) is a key ecophysiological parameter influencing leaf physiology, photosynthesis, and whole plant carbon gain. Both individual tree-based models and other forest process-based models are generally highly sensitive to this parameter, but information on its temporal or within-stand variability is still scarce. In a 2–4-year-old Eucalyptus plantation in Congo, prone to seasonal drought, the within-stand and seasonal variability in SLA were investigated by means of destructive sampling carried out at 2-month intervals, over a 2-year period. Within-crown vertical gradients of SLA were small. Highly significant relationships were found between tree-average SLA (SLA_t) and tree size (tree height, H_t, or diameter at breast height, DBH): SLA_t ranged from about 9 m² kg^?1 for dominant trees to about 14–15 m² kg^?1 for the smallest trees. The decrease in SLA_t with increasing tree size was accurately predicted from DBH using power functions. Stand-average SLA varied by about 20% during the year, with lowest values at the end of the 5-month dry season, and highest values about 2–3 months after the onset of the wet season. Variability in leaf water status according to tree size and season is discussed as a possible determinant of both the within-stand and seasonal variations in SLA.     

Polymerization of 1-naphthol and related phenolic compounds by an extracellular fungal enzyme

An extracellular phenol oxidase was isolated from the culture filtrate of the fungus Rhizoctonia praticola by gel filtration on Sephadex G-200. The enzyme catalyzed the polymerization of 1-naphthol to dimeric, trimeric, tetrameric, and pentameric compounds as determined by mass spectrometry. One product with a molecular weight of 286 was identified as 4,4′-bi-1-naphthol. Other compounds that were dimerized or polymerized by the enzyme were phenol, o-methoxyphenol (guaiacol), p-methylphenol (p-cresol), 2,6-dimethoxyphenol, and 1,3- and 1,5-dihydroxynaphthalene. The product from 2,6-dimethoxyphenol was isolated and identified as 3,5,3′,5′-tetramethoxydiphenoquinone.     

Impact of agroforestry practices on the flowering phenology of <Emphasis Type="Italic">Vitellaria paradoxa</Emphasis> in parklands in southern Mali

The impact of human practices on the phenology of flowering was assessed for an important agroforestry tree species of the Sudano-Sahelian zone: Vitellaria paradoxa. Flowering was monitored at two sites in southern Mali over 2 years. At each site, the impact of agricultural practices on flowering phenology was assessed by comparing field, fallow and forest. The site effect and agricultural practices were significant for all the monitored variables. The proportion of individuals that flowered was 89% at Koumantou and 40% at MPeresso. About 98, 95 and 75% of individuals at Koumantou and 88, 12 and 20% at MPeresso flowered in the field, fallow and forest, respectively. The mean length of flowering ranged from 69 to 81 days at Koumantou and from 45 to 108 days at MPeresso. The mean number of days for the active phase ranged from 36 to 49 days at Koumantou and from 27 to 64 days at MPeresso. Koumantou’s favourable climatic conditions resulted in better flowering ability and a higher probability of abundant flowering. Field appeared to provide better conditions than fallow and forest regarding flowering ability and probability of abundant flowering. However, tree diameter did not affect flowering phenology. Agricultural practices appear to have a noticeable impact on the phenology of flowering of V. paradoxa. Trees flowered abundantly in the parkland and therefore increased gene flow via pollen and/or seeds and the dynamics of genetic diversity.     

Comparative analysis of genetic diversity in Tunisian apricot germplasm using AFLP and SSR markers

Eighty-one accessions representing apricot germplasm in Tunisia were collected from different areas of cultivation and fingerprinted using amplified fragment length polymorphism (AFLP) and microsatellites (SSR) markers. A total of 339 polymorphic markers were revealed using 5 AFLP primers combinations and 24 SSR loci. AFLP and SSR markers expressed a high level of polymorphism allowing the distinction of the accessions with an efficiency coefficient of discrimination of 100% for AFLP and 97% for SSR markers. Genetic diversity structure was assessed with AFLPs and SSRs markers separately then with combined matrix data by the help of hierarchical clustering elaborated using Wards method based on Nei and Li (1979) distances. Comparison of the obtained dendrograms revealed a phylogeographic structure into two major groups with significant conservation between the observed subgroups in relation with the geographic origin of the accessions. The relative efficiency of the markers in determining the genetic relationships among apricot accessions has been assessed and a combination of AFLPs and SSRs markers was the most effective. In addition, Mantel test based on genetic distances indicated highly significant correlation between AFLP-SSR data and each of the AFLP and SSR ones, with Pearson correlation values of r = 0.873 and r = 0.692, respectively, revealing the higher efficiency of the combination of both molecular techniques (AFLP and SSR) to estimate the levels of genetic variability among apricot germplasm.     

From the recent lessons of the Malagasy foci towards a global understanding of the factors involved in plague reemergence

Re-emergence of human cases of plague after decades of silence does not necessarily mean that plague foci are re-emerging. Most often, Yersinia pestis bacteria have been maintained and circulating at low levels in the rodent populations. It seems therefore more appropriate to speak in terms of expansion or regression phases for sylvatic rodent plague foci and to reserve the term re-emergence for human cases. From the analysis of well-documented human plague cases in Madagascar, we underline the causes of re-emergence that can be generalized to most world foci, and can help define environments at risk where the threat of new emergence lurks. In all recent plague outbreaks, usually more than one risk factor was at the origin of the re-emergence. The reduction or discontinuance of surveillance and control, as well as poverty and insalubrity are the main factors in the re-emergence of human cases, allowing increased contacts with infected rodents and fleas. Environment changes (i.e. climatic changes, deforestation, urbanization) induce changes in flea and rodent populations by (i) extension of rodent habitats (for example by replacing forests by steppes or farmlands); (ii) modifications in population dynamics (possible outbreaks due to an increase of available food resources); but also, (iii) emergence of new vectors, reservoirs and new Y. pestis genotypes. Numerous and spontaneous genomic rearrangements occur at high frequencies in Y. pestis, which may confer selective advantages, enhancing the ability of Y. pestis to survive, to be transmitted to new hosts, and to colonize new environments. Therefore, any environmental change should be taken as a warning signal and active surveillance programs should be initiated.     

Efficacy of insecticide mixtures against larvae of Culex quinquefasciatus (Say) (Diptera: Culicidae) resistant to pyrethroids and carbamates

The efficacy of insecticide mixtures of permethrin (pyrethroid) and propoxur (carbamate) was tested by larval bioassays on two strains of Culex quinquefasciatus (Say), one resistant to pyrethroids and the other resistant to carbamates. The method consisted in combining one insecticide at the highest concentration causing no mortality (LC0) with increasing concentrations of the second one. The concentration-mortality regression lines were determined for permethrin and propoxur alone and in combination, and synergism ratios (SR) were calculated in order to determine the magnitude of an increase or decrease in efficacy with use of the mixtures. With the pyrethroid-resistant strain (BK-PER), the results showed that propoxur at LC0 significantly enhanced the insecticidal activity of permethrin (SR50 = 1.54), especially on the upper range of the concentration-mortality regression. Conversely, when permethrin at LC0 was tested with propoxur against the carbamate resistant strain (R-LAB), an antagonistic effect was observed (SR50 = 0.67). With the BK-PER strain, an increased oxidative detoxification (MFO) appeared to be the main mechanism responsible for the synergistic interaction. Nevertheless, antagonism in the R-LAB strain is probably due to a physiological perturbation implying different target sites for pyrethroid (ie sodium channel) and carbamate insecticides [ie acetylcholinesterase (EC 3.3.3.7) and choline acetyltransferase (EC 2.3.1.6)].     

Degradation of Sevin by soil microorganisms

Microorganisms capable of transforming the pesticide 1-naphthyl N-methyl-carbamate (Sevin) were isolated from soil. Three isolates were able to accelerate the hydrolysis of Sevin to 1-naphthol. Several unidentified intermediates were separated by thin-layer chromatography and also by following the decomposition of Sevin-methyl-¹⁴C. Since 1-naphthol is a biological as well as a chemical decomposition product of Sevin, its transformation by the isolated microbes was also studied. A fungus, identified as Fusarium solani, altered 1-naphthol rapidly. Whereas one strain of bacterium degraded the hydrolysis product gradually, another strain accumulated it under certain conditions. Mixed cultures of the investigated microbes were more effective in transforming Sevin than pure cultures, and this phenomenon was also observed with 1-naphthol as substrate with the exception of one bacterial strain.