Temperature-dependent development and survival of Podisus maculiventris (Hemiptera: Pentatomidae): implications for mass rearing and biological control

The spined soldier bug, Podisus maculiventris (Say), is a generalist predator that can control >75 insect pests in various agroecosystems. Despite valuable results from the previous studies, thermal development and survival of P. maculiventris over a wide range of temperatures had not been elucidated completely. This study was conducted to investigate the stage-specific development and survival of P. maculiventris at eight constant temperatures (13.2, 18.4, 21.7, 23.7, 27.2, 32.7, 35.2, and 40.6 °C) covering the entire thermal range for P. maculiventris development. Completion of egg development was observed at 13.2–32.7 °C, whereas nymphs successfully developed into adults at 18.4–32.7 °C. Survival model using log-normal equations showed bell-shape patterns for all stages, and temperatures resulting in highest survival of P. maculiventris were 19.9, 24.3, and 24.5 °C for egg, nymph, and egg to adult, respectively. Developmental rates at the eight temperatures were fitted with a nonlinear Briere model, which estimated optimal temperatures for development as 31.2, 30.6, and 30.6 °C for egg, nymph, and egg to adult, respectively. Operative thermal ranges (i.e., in-between the lower and upper developmental thresholds) were estimated to be 8.9–35.2, 12.8–35.2, and 12.7–35.2 °C for egg, nymph, and egg to adult, respectively. In a linear model, the lower thresholds were 10.9, 13.1, and 13.0 °C for egg, nymph, and egg to adult, respectively. Findings herein provide comprehensive data and explanations on optimal temperature and thermal requirement for P. maculiventris, which can be used to optimize environmental condition in mass rearing and predicting phenology of P. maculiventris in the field.     

工厂化繁育香菇胶囊菌种专用培养基配方研究

在已筛选出的代料香菇胶囊菌种专用配方LSC1和LSC5基础上,设计了7种香菇胶囊菌种培养基配方,以L26为供试菌株,观察测试了菌丝生长速度、瘤状突起物形成时间与数量、菌种成型及在愈伤培养时的特征以及菌种持水性等特征指标,筛选出了适宜于工厂化繁育香菇胶囊菌种的专用培养基配方LSCG2T和LSCG3,并在胶囊菌种工厂化繁育生产线中进行了应用试验,取得了良好效果。试验结果表明,工厂化繁育胶囊菌种的配方中粗细木屑的比例应提高到5∶1,配方中应添加以提供微量元素和基质物理性能改良剂的辅料。     

Prediction of bending properties for structural glulam using optimized distributions of knot characteristics and laminar MOE

This study established a prediction model for bending properties of glued-laminated timber (glulam) using optimized knot and modulus of elasticity (MOE) distributions of lumber laminate as the main input variables. For this purpose, knot and MOE data were investigated for all pieces of lumber that were prepared for glulam manufacturing, and statistical distributions of knot size, knot number in one lumber, and MOE of each laminate were optimized as distribution functions. These knot and MOE data were used as input variables in the prediction model for bending properties, and were also used in generating virtual glulam using the inverse transform method. Prediction of bending properties for glulam was carried out using the transformed section method, which is partially provided in ASTM D 3737 (Annex A4). Predicted values were compared with those from full-scale four-point bending tests for 60 six-layered glulams with 10 different laminar combinations. Finally, the allowable bending properties of glulam for each specific laminate combination were determined by calculating the fifth percentile of the modulus of rupture and the average modulus of elasticity from virtual test results of more than 1000 virtual glulams. From the results of this study, predicted bending properties for glulam and their distributions could be used for structural design in both allowable stress design and limit state design.     

Intergeneric hybrids and an amphiploid between Elymus canadensis and Psathyrostachys juncea

Summary Fifty four hybrid plants between Elymus canadensis and Psathyrostachys juncea were obtained by handpollination and embryo culture. The average cross compatibility between both species was 31.2 percent. One amphiploid plant was induced by colchicine treatment. The hybrid and amphiploid plants resembled P. juncea in appearance but showed a higher plant height and dry matter yield than the parents. The hybrids showed extremely low pollen stainability and were completely sterile. With the exception of one plant (2n=3x+1=22), all hybrid plants were allotriploids (SHN, 2n=3x=21). The amphiploid plant (SSHHNN, 2n=6x=42) showed 58.9% pollen stainability and 11.6% seed fertility.Mean chromosome associations of the hybrids and amphiploid at metaphase I were 0.02IV+0.06III+2.03II+16.91I and 0.07III+18.00II+5.85I, respectively. Lagging chromosomes, chromosome bridges, abnormal cytokinesis, and micronuclei were occasionally observed at the anaphase, telophase, or tetrad stage.     

The Giemsa C-Banded Karyotype of Canada Wildrye (Elymus canadensis)

Karyotype of Canada wildrye (Elymus canadenisis L.) was described using giemsa C-banding techniques. Most of the chromosomes showed dome banding pattern polymorphism. Small to large terminal and centormere bands were observed in most of the chromosomes. A faint satellite was observed in one chromosome. Tow chromosomes had a large interstitial band near the centromeres in the long arms. The Giemsa C-banding pattern of E. Canadensis is compared to that of Pseudoroegneria spicata and Critesion boddanii to illustrate species relationship.     

The use of microsatellite polymorphisms to characterise and compare genetic variability in Avena strigosa and A. barbata

Microsatellite (SSR) polymorphism was assessed across 90 diploid Avena strigosa Schreb. and tetraploid Avena barbata Pott ex Link accessions obtained from the USDA-ARS National Small Grains Collection using 105 genomic SSRs. Eleven polymorphic SSRs that detected 69 different alleles were identified and used to genotype the 90 accessions, which were chosen from a larger set of 385 accessions based on geographical source-diversity and variable reaction responses to five Australian pathotypes of the crown rust pathogen Puccinia coronata Corda f. sp. avenae Eriks. Eight diploid and eight tetraploid clades were identified among the 90 accessions. Diploid accessions displayed the lowest genetic diversity, with all accessions being at least 86 % similar, and included accessions from countries in the Americas such as Canada, USA, Argentina, Uruguay and Brazil, and European accessions from France, Romania and Poland. Although both species formed distinct clusters in the dendrogram, a few instances of diploids showing high similarity with tetraploids and vice versa were observed. An AMOVA analysis revealed 86 % of the total genetic variation to be distributed within the two oat species, while between-species differences accounted for only 14 %. Heterozygosity (H) index values of 0.32 and 0.40 were obtained for diploids and tetraploids respectively. Our study effectively differentiated A. strigosa and A. barbata, and identified 11 SSRs suitable for future characterisation of accessions of the two species.     

Methylation methods for the quantitative analysis of conjugated linoleic acid (CLA) isomers in various lipid samples

Precise methylation methods for various chemical forms of conjugated linoleic acid (CLA), which minimize the formation of t,t isomers and allylmethoxy derivatives (AMD) with the completion of methylation, were developed using a 50 mg lipid sample, 3 mL of 1.0 N H(2)SO(4)/methanol, and/or 3 mL of 20% tetramethylguanidine (TMG)/methanol solution(s). Free CLA (FCLA) was methylated with 1.0 N H(2)SO(4)/methanol (55 degrees C, 5 min). CLA esterified in safflower oil (CLA-SO) was methylated with 20% TMG/methanol (100 degrees C, 5 min), whereas CLA esterified in phospholipid (CLA-PL) was methylated with 20% TMG/methanol (100 degrees C, 10 min), followed by an additional reaction with 1.0 N H(2)SO(4)/methanol (55 degrees C, 5 min). Similarly, CLA esterified in egg yolk lipid (CLA-EYL) was methylated by base hydrolysis, followed by reaction with 1.0 N H(2)SO(4)/methanol (55 degrees C, 5 min). These results suggest that for the quantitative analysis of CLA in lipid samples by GC, proper methylation methods should be chosen on the basis of the chemical forms of CLA in samples.     

Botanical origin and chemical composition of Brazilian propolis

Brazilian propolis has been classified into 12 groups based on physicochemical characteristics: five in the southern Brazil group (group 3), one in the southeastern Brazil group (group 12), and six in the northeastern Brazil group (group 6). The plant origins of these groups were investigated using reversed-phase high-performance thin-layer chromatography (RPHPTLC), reversed-phase high-performance liquid chromatography (RPHPLC), and gas chromatography-mass spectrometry (GC-MS). It was concluded that the origins of propolis group 3, group 6, and group 12 are resins of the poplar tree, Hyptis divaricata, and Baccharis dracunculifolia, respectively.     

Structure of a new echinocystic acid bisdesmoside isolated from Codonopsis lanceolata roots and the cytotoxic activity of prosapogenins

We isolated a new saponin named codonoposide (1) from the roots of Codonopsis lanceolata (Campanulaceae) and characterized it as 3-O-[beta-D-xylopyranosyl(1-3)-beta-D-glucuronopyranosyl]-3beta,16alpha-dihydroxyolean-28-oic acid 28-O-[beta-D-xylopyranosyl (1-3)-alpha-L-rhamnopyranosyl (1-2)-alpha-L-arabinopyranosyl] ester by chemical, physicochemical, and 2DNMR techniques. Complete hydrolysis of 1 produced a sapogenin (1a), and the partial hydrolysis and further isolation afforded two prosapogenins (1b, 1c). The structures of 1a, 1b, and 1c were found to be 3beta,16alpha-dihydroxyolean-28-oic acid (echinocystic acid, 1a), 3-O-beta-D-glucuronopyranoside of 1a, and 3-O-beta-D-xylopyranosyl (1-3)-beta-D-glucuronopyranoside of 1a, respectively, on the basis of spectroscopic data. On MTT assay, 1a showed marginal cytotoxic activity whereas 1b exhibited more cytotoxicity than 1a. However, the bisdesmosylsaponin 1 exhibited no cytotoxicity (IC(50)>0.3 mM against tested cell lines). This result indicated that glycoside linkage of glucuronic acid at C-3 enhances the cytotoxicity of sapogenin (1a), and additive glycosylation of xylose to 1b strongly enhances the cytotoxicity of 3-O-monosaccharides (1b). Therefore, true forms of codonoposide for the cytotoxicity must be sapogenins or prosapogenins.