Suppression of green peach aphid (Myzus persicae) (Sulz.), citrus mealybug (Planococcus citri) (Risso), and two spotted spider mite (Tetranychus urticae) (Koch.) attacks on tomatoes and cucumbers by aqueous extracts from vermicomposts

Vermicomposts are produced through interactions between earthworms and microorganisms in the breakdown of organic wastes. Aqueous extracts were prepared in commercial brewing equipment (Growing Solutions Inc.) from vermicomposts processed from pre-consumer food waste. The ratio of vermicompost to water was 1 to 5 v:v to produce a 20% aqueous solution. The effects of soil drenches at dilutions of 20%, 10%, and 5% vermicompost extracts, were compared with those of deionized water, in the suppression of green peach aphids, mealybugs, and two spotted spider mites attacking tomatoes and cucumbers, in greenhouse cage experiments.     

Suppression of Botryosphaeria canker of apple by arbuscular mycorrhizal fungi

Stem brown canker or Botryosphaeria canker disease impairs the growth and kills the shoots, limbs and even trunks of infected apple trees. Apple roots are usually colonized by arbuscular mycorrhizal fungi, which may have a positive influence on plant growth and suppression of diseases. In order to assess the efficacy of AM to suppress the disease severity and plant growth enhancement, nine AMF inoculation treatments (Sclerocystis dussi, Glomus intraradices, G. fasciculatum, G. bagyaraji, G. leptotichum, G. monosporum, Gigaspora margarita, a mixed AM culture and a non-mycorrhizal control treatment) were used in this present study. Two-year-old potted apple plants, maintained under glasshouse conditions, were either pre-inoculated with AMF followed by stem inoculation with Botryosphaeria ribis or simultaneously inoculated with Botryosphaeria ribis and AM. The results indicated that the incidence of canker was less severe in plants inoculated with AMF in comparison to non-mycorrhizal control. Timing of inoculation also had a significant effect on disease development and plant survival. Plants pre-inoculated with mycorrhiza performed better over those inoculated simultaneously with Botryosphaeria ribis and AM fungi. Furthermore, AM inoculation resulted in improved survival and growth of AMF-colonized plants; though, it varied by species of AM fungi utilized.     

Assessment of genetic divergence in salt tolerance of soybean (<Emphasis Type="Italic">Glycine max</Emphasis> L.) genotypes

A large number of soybean (Glycine max L.) genotypes of diverse growth habit and adaptive characters were used in the experiment. Soil salinity-induced changes in nine morpho-physiological characters of 30-day-old seedlings of 170 soybean genotypes were compared in the study. The first and second principal components (PC) of principal component analysis (PCA) results accounted for 97 and 2.5%, respectively, of the total variations of soybean genotypes. The variation for the first PC was composed mainly of relative total dry weight (DW), relative shoot dry weight, as well as petiole dry weight. There were four clusters distinguished in the cluster analysis. The genotypes in cluster IV performed better in respect to relative total dry weight and relative shoot dry weight and hence having salt tolerance. The genotypes clusters III performed very poorly and those of clusters II and I were moderate to poor. D2 analysis indicated that the clusters differed significantly from each other. Discriminant function analysis (DFA) again asserts strongly that more than 92% of the genotypes were correctly assigned to clusters. Both PCA and DFA confirmed that the relative total DW followed by shoot and petiole DW were the major discriminatory variables, and the root DW were the secondary important variables to distinguish genotypes into groups. In this study, multivariate analyses were used in identifying the soybean genotypes of desirable traits for salt tolerance.     

Economics and Employment Generation of Bamboo-Based Enterprises: A Case Study from Eastern Bangladesh

An exploratory survey was carried out to assess economics and employment generation of the trade of bamboo and bamboo-based secondary products in the eastern Bangladesh, to obtain reliable information about their status, socio-economic significance, production and marketing. The study was undertaken over 30 bamboo-based enterprises in a suburban market of eastern Bangladesh, to investigate regional product details, economic profitability and employment opportunities. The sample entrepreneurs, corresponding to about 25% of the bamboo enterprise population were interviewed using a semi-structured questionnaire. About 202 full and part-time workers were employed in the factories, under categories of artisan (who manufactured secondary products). The average number of worker’s in the large, medium and small factories were 9 (artisan 40%), 6.45 (artisan 35%) and 5 (artisan 25%) respectively. The study revealed that there was always a satisfied demand of skilled artisans. Most of the workers were relatively newly employed (not more than 5 years). The daily wage rate varied between 70 and 130 Tk. ($US 1 equals approximately 70 Bangladeshi Taka (Tk.), as at December 2008). Bambusa balcooa was the most utilized species (39.96%) in terms of monetary value. The price of a single B. balcooa culm in the local market was Tk. 160–210. Nine sizes of articles under seven bamboo categories were identified, these being bera (36″ × 120″ and 72″ × 96″), bookshelf (36″ × 24″), chaluni (12″ × 12″), chatai (48″ × 60″ and 36″ × 48″), jhuri, rickshaw hood and tukri. Net average profit per article was the highest for rickshaw hoods (Tk. 400 at the retailer stage). The total expected annual income for an enterprises from all articles types sold was estimated to be Tk. 85,800. Three distinct marketing channels were identified for selling bamboo and value-added secondary products. The study also generated policy implications for effective management of bamboo-based enterprises.     

<Emphasis Type="Italic">Eimeria bovis</Emphasis> meront I-carrying host cells express parasite-specific antigens on their surface membrane

Host immune responses conducted against antigens of Eimeria bovis are key factors for the development of protective immunity against this protozoan disease. In this study we investigated the expression of E. bovis-derived antigens on the host cell surface membrane during E. bovis first merogony in vitro. Host cells carrying E. bovis-meront I stages expressed E. bovis host cell surface antigens (EbHCSAg) on their surface membrane which were recognised by hyperimmune sera of calves and by sera from rats immunized with E. bovis merozoites I, when tested by indirect immune fluorescent antibody test (IIFAT), laser scanning confocal microscopy (LSCM) and immune electron microscopy. Expression of EbHCSAg on permissive host cells was earliest detected 7 days p. i., thus coinciding with the onset of the parasite replication. Membrane-associated EbHCSAg were removed from infected host cells by proteinase K, partially by Triton X-100, Triton X-114 and Triton X-405, but not by 1 M NaCl, CHAPS or phospholipase C treatment. Antibodies, affinity-purified on paraformaldehyde/glutardialdehyde (PAGA)-fixed E. bovis meront I-infected bovine host cells bound to the surface meront I-carrying cells and to merozoites I (IIFAT, LSCM) but, in contrast to untreated sera, not to sporozoites. When tested on methanol-fixed merozoites I and sporozoites by IIFAT, affinity-purified antibodies bound to structures in the apical complex area of merozoites I, but not to sporozoites, whilst untreated sera caused diffuse labelling of internal structures of both parasite stages. Immune electron microscopy demonstrated binding of affinity-purified antibodies to micronemes and dense granules of merozoites I. Although the function of EbHCSAg is still unknown, results of this study might suggest an involvement in the development of protective immunity against E. bovis infections.     

Cytoarchitectural differences of myoepithelial cells among goat major salivary glands

Previously, the distribution of myoepithelial cells (mecs) in the salivary glands was studied by both immunohistochemistry, and transmission electron microscopy; however, little was elucidated concerning their morphological features, especially in goats. This study was performed to investigate the correlation between the cytoarchitecture of the mecs in goat major salivary glands (parotid, mandibular, and sublingual glands) and the nature of the saliva secretion. The cytoarchitectural features of the mecs were examined by scanning and transmission electron microscopy as well as immunohistochemically. The secretory endpieces in the parotid gland are of the pure serous type, but in both the mandibular and sublingual glands they are of the mixed type. In all studied glands, the intercalated ducts were covered by mecs which, unlike the large stellate cells that surrounded the secretory endpieces, were spindle-shaped with few cytoplasmic processes. Interestingly, the mecs were found to bulge on the basal surfaces of the serous acini and intercalated ducts in all glands and to be in close contact to the seromucous tubules surface in the mandibular and sublingual glands forming a continuous network around it. In conclusion, the differences in the degree of development of the mecs as well as the number of their cytoplasmic processes may be correlated with the nature of the secretion and the number of the secretory granules. Thus these observations may have some relevance in the diagnosis of atrophy and pathogenic conditions of these glands.     

Molecular characterization and marker based chemotaxonomic studies of Podophyllum hexandrum Royle

Detailed chemical studies and RAPD analysis were done in different populations of Podophyllum hexandrum collected from high altitude regions of North Western Himalayas. Random amplified polymorphic DNA (RAPD) analysis revealed a high degree of genetic diversity among the 12 collected accessions, attributed to their geographical and climatic conditions. HPLC analysis also revealed variation in the concentration of two major marker compounds which lead to the identification of a chemotype. The study demonstrated that RAPD and chemical markers are very useful tools to compare the genetic relationship and pattern of variation among such prioritized and endangered medicinal plants.     

Molecular polymorphism of cytoplasmic DNA in Ficus carica L.: Insights from non-coding regions of chloroplast DNA

The trnL (UAA) intron and the intergenic spacer between the 3′ exon of trnL (UAA) and trnF (GAA) sequences were used as genetic markers for differentiating Ficus carica cultivars and establishing refined genetic relationships. The study was based on 20 fig cultivars, collected from south and centre of Tunisia. Since, the intron was thought to be more variable among close relatives than is the chloroplast spacer. The size of these non-coding regions varied from 554 to 589 and from 989 to 1022 bases pairs for the intron and the combined sequences correspondingly. The average of GC content was 33.9% and 34.6% in the intron and the combined intron and spacer respectively. High values of A + T contents were detected in both data sets and may explain the high proportions of transversions founded. The observed variation pattern of plastid DNA provides evidence of an important genetic diversity. The overall transition/transversion bias (R) was 0.202 in the intron and 0.27 in the combined regions. The RI index of 0.592 indicates that these combined sequences have clearly more homoplasy then the intron (RI = 0.705) and spacer (RI = 0.777) sequences separately. Phylogenetic trees were generated based on maximum parsimony (MP) and neighbor-joining (NJ) analysis of the chloroplast sequences data. Results proved that a typically continuous genetic diversity characterizes the local fig germplasm. In fact, relationships inferred from the cpDNA analysis suggest several clades, which do not show geographical or tree sex correspondence. Although the level of apparent diversity is considerable, we may conclude that non-coding regions of chloroplast genome provide a new and practical opportunity to evaluate genetic diversity and to discriminate fig cultivars. Revealed cytoplasmic DNA markers are reliable to elaborate a molecular data base to conduct management and breeding programs on local fig germplasm.