Quantitation of malaria sporozoites transmitted in vitro during salivation by wild Afrotropical Anopheles

Abstract. The malaria transmission potential of wild, infective Anopheles from western Kenya was evaluated by determining the number of sporozoites transmitted in vitro by salivation when their mouthparts were inserted into capillary tubes containing either sucrose or blood. With sucrose, 86.6% of 102 infective Anopheles transmitted a geometric mean (GM) of 3.84 sporozoites (range 1–34). With blood, 23.1% of 104 infective Anopheles , tested on the day of collection, transmitted a GM of 2.30 sporozoites (range 1–117). For Anopheles held 5 days postcapture before testing with blood, 53.6% of 56 transmitted a GM of 6.04 sporozoites (range 1–420). Transmitting Anopheles contained significantly more salivary gland sporozoites than non-transmitters. No significant differences were detected between Anopheles gambiae Giles sensu lato and Anopheles funestus Giles in sporozoite transmission by individuals with sporozoites in their salivary glands.
Sporozoites were detected microscopically in the salivary duct from heads in 80.3% of 117 infective Anopheles (GM=11.2, range 1–71). Sporozoite detection in mosquito heads by ELISA was 25% less efficient than microscopic detection.
Over 98% of the infective Anopheles transmitted less than twenty-five sporozoites. Transmitted sporozoites represented only about 3% of the total sporozoites in the salivary glands suggesting that sporozoite transmission may be restricted to sporozoites in the salivary duct at the time of feeding. Results are discussed in relation to anti-sporozoite vaccine development.     

Examination of the 'founder effect' in biodiversity research: patterns and imbalances in the published literature

We reviewed 2524 articles published from 1987 to 1995 in five international journals, Conservation Biology , Biological Conservation , Biodiversity and Conservation , Ecological Applications , and the Journal of Applied Ecology , to assess patterns and imbalances in biodiversity research in the following subject areas: locations where research was conducted, types of organisms studied, types of ecosystems studied, types of methodologies used, and types of stresses investigated. Biodiversity research was found to be narrowly focused with little deviation from its initial course set of being a discipline concerned largely with the implications of forest habitat loss on charismatic terrestrial megafauna; i.e. the 'founder effect' is very much in evidence. The 'sleeping dragon' of ignored marine biodiversity is really symptomatic of a wider problem, and can perhaps be referred to as a 'hibernating hydra' of many imbalances due to, for example, under-representations of research from developing nations, or on amphibians and invertebrates, alpine and arctic systems, sociological components and chemical stresses etc. It is time to take steps to actively awaken the creature so that conservation biology/applied ecology can become more pluralistic in scope.     

Calcification in the bivalve periostracum

The periostracum in certain bivalves is imbedded with calcified, spiculelike structures analogous if not homologous to cuticular spicules found in the Aplacophora and Polyplacophora (chitons). Although rare or absent in most living bivalves, calcified periostracal structures are apparently an ancestral feature in some bivalve groups, i.e. the Mytilacea, Permophoridae, Myoida. and Anomalodesmata. Ancestors of the Bivalvia and Polyplacophora may have been covered with a flexible, spiculestudded cuticle. Shell plates in these two classes may have originated through a modification of the mechanism of spiculelike cuticular calcification. resulting in a primordial shell with simple prismatic structure.     

Host plant variation in mortality of the leaf-folding sawfly on the arroyo willow

Abstract. 1. We tested the hypothesis that survival and sources of mortality of the leaf-folding sawfly ( Phyllocolpa sp.) varied significantly among host plants of the arroyo willow ( Salix lasiolepis Bent ham).
2. Survival of the leaf folder differed among field and potted willows in a common environment in two of three cases, and sources of mortality differed among plants in four of five cases.
3. Egg mortality differed among field plants but not among the potted willow plants.
4. Larval mortality and parasitism differed among field and potted willows in 2 years, and appeared to be compensatory mortality sources.
5. Leaf folder density among plants was not generally correlated with percentage of leaf folds with no egg (galls formed but no subsequent oviposition), percentage survival, or percentage mortality, indicating a general lack of density dependence.
6. The proportion of folds with no egg oviposited differed significantly among field and potted plants, and was only correlated with survival or sources of mortality in one of three years.
7. The data support the hypothesis that host plant genotype affects the interaction of the leaf folder with its natural enemies, and thus represents a three trophic level interaction.     

Diurnal Changes in Asparaginase Activity in Pea Leaves: II. REGULATION OF ACTIVITY

Pea leaf asparaginase is stabilized by asparagine and aspartateduring incubation. In crude extracts this effect was enhancedby products of the light reaction (NADPH, NADH, or reduced ferredoxin),but these compounds were ineffective on the purified enzyme,or in the absence of asparagine. MgATP, MgADP and oxidized ferredoxinreduced asparaginase activity in purified preparation reducedor oxidized glutathione had no effect. Asparaginase activitydoes not appear to be modulated via phosphorylation/dephosphorylation.The presence of calcium during extraction increased asparaginaseactivity more than 2-fold, but addition of calcium to extractsprepared in its absence had no effect; calmodulin had no effecton activity. Co-extraction of light- and dark-treated tissueshowed that soluble factors are not responsible for the diurnalvariation in asparaginase activity. Association of asparaginasewith membranes did not account for changes in extractable activity.Use of the protein synthesis inhibitors cycloheximide, puromycin,emetine, actinomycin D and cordycepin and the thiol proteaseinhibitor leupeptin suggested that mRNA and protein synthesisare required for the increase of asparaginase activity duringthe light period and that proteolytic degradation accounts forthe decrease during the dark. Key words: Pisum sativum, asparaginase, protein synthesis, proteolysis.     

Diurnal Changes in Asparaginase Activity in Pea Leaves: I. THE REQUIREMENT FOR LIGHT FOR INCREASED ACTIVITY

During the growth of leaves of Pisum sativum L., levels of asparaginase(E.C. 3.5.1.1 [EC] ) showed a diurnal variation during a 3 d periodof leaf expansion, increasing in the light and decreasing inthe dark period; the greatest diurnal variation being foundin half-expanded leaves. Asparaginase activity in half-expandedleaves reached a maximum after 4 h exposure to light and thisactivity was maintained over the rest of the light period. Changesin asparaginase activity were not influenced by diurnal temperaturechanges. The increase in asparaginase activity during the lightperiod was directly proportional to the photon flux densityover the range 0–285 µmol m^-2 s^-1 PAR. The increaseof asparaginase activity during illumination of detached leaveswas inhibited by the photosynthetic electron transport inhibitors3-(3', 4'-dichlorophenyl)-1, 1-dimethylurea (DCMU) and atrazine.These observations indicate that the increase in asparaginaseactivity in half-expanded leaves is dependent upon non-cyclicelectron transport. Key words: Pisum sativum, asparaginase, photosynthetic electron transport