Development of the red palm weevil, Rhynchophorus ferrugineus (Olivier), (Coleoptera, Curculionidae) on natural and synthetic diets

The development of the red palm weevil, Rhynchophorus ferrugineus (Olivier) was investigated on a newly developed semiartificial diet as compared with two natural diets namely sugarcane stem and banana fruit. The weevil was successfully maintained on these diets and duration of the life cycle for males and females, respectively were 164.97 and 194.61 days on the semiartificial diet, 192.5 and 186.5 days on banana, and 172.00 and 170.00 days on sugarcane. The average egg production per female was shown to be significantly higher on the semiartificial diet, being 184.00?±?18.68 eggs compared with an average of 125.00?±?11.97 and 133.00?±?15.21 eggs on banana and sugarcane, respectively. The fertility ranged between 94?–?100?% in those eggs deposited by females previously reared on the tested diets. The developed semiartificial diet was shown to be suitable for maintaining laboratory colonies of the red palm weevil, and it can substitute natural diets.     

In situ measurement of tensile elastic moduli of individual component polymers with a 3D assembly mode in wood cell walls

We attempted to measure in situ the tensile elastic moduli of individual component polymers with a three-dimensional (3D) assembly mode in the cell walls of Sugi (Cryptomeria japonica D. Don) without isolating the polymers. To prepare wood tangential slices [50 × 6 × 0.2 mm (L × T × R)] consisting of lignin with a 3D assembly mode in the cell walls, cellulose and hemicellulose were removed using the method of Terashima and Yoshida (2006) to obtain methylated periodate lignin slices. To prepare wood slices consisting of polysaccharide with a 3D assembly mode in the cell walls, lignin was removed using the method of Maekawa and Koshijima (1983) to obtain holocellulose slices. Static tensile test was applied to determine the elastic moduli of 3D lignin and 3D polysaccharide slices. The followings were revealed. The elastic modulus of the 3D lignin slices was 2.8 GPa, regardless of the microfibril angle (MFA) in the slices. The elastic moduli of the 3D polysaccharide slices with MFAs of 14°, 23°, 34°, and 42° were 18, 12, 9, and 4 GPa, respectively. The former shows that the lignin with a 3D assembly mode behaves as an isotropic substance in the cell walls, while the latter suggests that the 3D polysaccharide slice shows marked anisotropic structure in the cell wall. Despite the fact that cellulose content increased after lignin removal, values of substantial elastic modulus of the cell wall slightly decreased regardless of MFA. Following two possible reasons were pointed out for explaining this phenomenon. First, lignin removal caused an artifactual deterioration in the polysaccharide slices at the level of macromolecular aggregate. Second, rigid and fusiform-shaped cellulose crystallites are dispersed in the soft matrix of amorphous polysaccharide, and those are loosely connected to each other by the intermediary of matrix polysaccharide. Those suggest that the rigid cellulose crystallite can optimize its strong mechanical performance in the polysaccharide framework of the wood cell wall in combination with the ligninification.     

Short-term changes in the soil carbon stocks of young oil palm-based agroforestry systems in the eastern Amazon

The current expansion of the oil palm (Elaeis guineensis Jacq.) in the Brazilian Amazon has mainly occurred within smallholder agricultural and degraded areas. Under the social and environmental scenarios associated with these areas, oil palm-based agroforestry systems represent a potentially sustainable method of expanding the crop. The capacity of such systems to store carbon (C) in the soil is an important ecosystem service that is currently not well understood. Here, we quantified the spatial variation of soil C stocks in young (2.5-year-old) oil palm-based agroforestry systems with contrasting species diversity (high vs. low); both systems were compared with a ~10-year-old forest regrowth site and a 9-year-old traditional agroforestry system. The oil palm-based agroforestry system consisted of series of double rows of oil palm and strips of various herbaceous, shrub, and tree species. The mean (±standard error) soil C stocks at 0–50 cm depth were significantly higher in the low (91.8 ± 3.1 Mg C ha^?1) and high (87.6 ± 3.3 Mg C ha^?1) species diversity oil palm-based agroforestry systems than in the forest regrowth (71.0 ± 2.4 Mg C ha^?1) and traditional agroforestry (68.4 ± 4.9 Mg C ha^?1) sites. In general, no clear spatial pattern of soil C stocks could be identified in the oil palm-based agroforestry systems. The significant difference in soil carbon between the oil palm area (under oil palm: 12.7 ± 2.3 Mg C ha^?1 and between oil palm: 10.6 ± 0.5 Mg C ha^?1) and the strip area (17.0 ± 1.4 Mg C ha^?1) at 0–5 cm depth very likely reflects the high input of organic fertilizer in the strip area of the high species diversity oil palm-based agroforestry system treatment. Overall, our results indicate a high level of early net accumulation of soil C in the oil palm-based agroforestry systems (6.6–8.3 Mg C ha^?1 year^?1) that likely reflects the combination of fire-free land preparation, organic fertilization, and the input of plant residues from pruning and weeding.     

Above- and belowground carbon stocks of two organic,agroforestry-based oil palm production systems in eastern Amazonia

Ecosystem-level assessments of carbon (C) stocks of agroforestry systems are scarce. We quantified the ecosystem-level C stocks of one agroforestry-based oil palm production system (AFS_P) and one agroforestry-based oil palm and cacao production system (AFS_P+C) in eastern Amazonia. We quantified the stocks of C in four pools: aboveground live biomass, litter, roots, and soil. We evaluated the distribution of litter, roots, and soil C stocks in the oil palm management zones and in the area planted with cacao and other agroforestry species. The ecosystem-C stock was higher in AFS_P+C (116.7 ± 1.5 Mg C ha^?1) than in AFS_P (99.1 ± 3.1 Mg C ha^?1). The total litter-C stock was higher in AFS_P+C (3.27 ± 0.01 Mg C ha^?1) than in AFS_P (2.26 ± 0.06 Mg C ha^?1). Total root and soil C stocks (0–30 cm) did not differ between agroforestry systems. Ecosystem-C stocks varied between agroforestry systems due to differences in both aboveground and belowground stocks. In general, the belowground-C stocks varied spatially in response to the management in the oil palm and non-oil palm strips; these results have important implications for the monitoring of ecosystem-level C dynamics and the refinement of soil management.     

Changes in bamboo fiber subjected to different chemical treatments and freeze-drying as measured by nanoindentation

The effects of chemical treatments (H₂O₂ + CH₃COOH, acidified NaClO₂, and NaOH) and freeze-drying on bamboo fibers were studied at a submicron level, to characterize chemical and mechanical changes to the secondary cell wall. Specifically, a field emission environmental scanning electron microscope (FE-ESEM) and imaging fourier transform infrared spectroscopy (FTIR) were used to demonstrate degradation in morphology and molecular structure, and nanoindentation was used to track changes in micromechanical properties. The results showed that cellular structures after chemical treatments clearly displayed wrinkles, pores, and microfibrils. The decreased bands at 1508 cm^-1 and 1426 cm^?1 showed that lignin was degraded on treatment of H₂O₂ + CH₃COOH and acidified NaClO₂, which directly resulted in a decrease in hardness (H) in the secondary cell wall for treated fibers. In addition, a diminishing peak at 1733 cm^?1 caused by NaOH solution indicated that hemicellulose was seriously degraded. It resulted in a decreased modulus (E _r) by 13.71 % in bamboo fibers, while no obvious reduction was observed in the first two steps.     

Enzymatic hydrolysis of wood with alkaline treatment

Pulverized samples of wood, cedar and eucalyptus were treated with 5 N NaOH solutions at 25–150 °C. Hemicellulose and lignin content in the samples decreased with increasing treatment temperatures, while the recovery of glucose was maintained at nearly 90 %. X-ray diffraction analysis showed that the content of the original cellulose I structure in the samples decreased with increasing temperature, and most of the cellulose in the sample treated at 150 °C was converted to cellulose II by mercerization. Enzymatic hydrolysis of the alkaline-treated samples was carried out at 37 °C using solutions comprising a mixture of cellulase and β-glucosidase. The samples treated at higher temperatures showed better enzymatic degradability. Treatment with an alkaline solution of lower concentration (1 N NaOH) at 150 °C was also used. Despite significant quantities of hemicellulose and lignin being removed, mercerization was not induced. The enzymatic degradability was much lower than that of the sample treated with a 5 N NaOH solution at 150 °C. Thus, treatment with concentrated alkaline solution at high temperature led to not only the removal of hemicellulose and lignin, but also to modification of the cellulose structure, which resulted in high efficiency of enzymatic saccharification of the wood samples.     

Effect of the amount of lignin on tensile properties of single wood fibers

Chemical components are the main factors affecting the mechanical properties of wood fibers. Lignin is one of the main components of wood cell walls and has a critical effect on the mechanical properties of paper pulp and wood fiber based composites. In this study, we carried out tensile tests on single mature latewood tracheids of Chinese fir (Cunninghamia lanciolata (Lamb.) Hook.), using three different delignified treatment methods to obtain different amounts of lignin. We applied single fiber tests to study the effect of the amount of lignin on mechanical tensile properties of single wood fibers at the cellular level. The results show that in their dry state, the modulus of elasticity of single fibers decreased with the reduction in the amount of lignin; even their absolute values were not high. The amount of lignin affects the tensile strength and elongation of single fibers considerably. Tensile strength and elongation of single fibers increase with a reduction in the amount of lignin.     

Comparative studies on microstructures and chemical compositions of cell walls of two solid wood floorings

Two common wood flooring materials, taun (Pometia spp.) and cumaru (Dipteryx odorata), were used as investigated objects and comparison was made between the two wood species for their density, microstructure, microfibril angle (MFA), cellulose crystallinity and the main chemical composition. Results showed that the density of cumaru was 0.941 g·cm^?3, significantly larger than that of taun, 0.737 g·cm^?3. The biggest difference of two wood species in microstructures was fiber cells. Fiber cells of cumaru had dense cell walls, almost no cell lumens; while fiber cells of taun had relatively thin cell walls, with apparent cell lumens. The thickness of fiber cell wall of cumaru and taun were 6.80 and 2.82 µm, respectively, and the former is about 2.5 times thicker than the latter. Measured data of MFA indicated that the average MFA of cumaru was 11.7°, smaller than that of taun, 13.4°. The relative crystallinity of cumaru and taun were 54.0 and 50.8%, respectively. The two wood species had the similar holocellulose contents, but the lignin content of cumaru was higher than that of taun, especially that the content of extractive of cumaru was as twice as that of taun.     

Chemical composition of lignocellulosic biomass in the wood of <Emphasis Type="Italic">Abies religiosa</Emphasis> across an altitudinal gradient

Tree adaptation to environment has been extensively studied. However, little is known about the variations in structure and chemical composition of lignocellulosic biomass (LB) in relation to altitudinal gradient. We wonder, are there significant variations in the LB in the wood across an altitudinal gradient? To answer this, we carried out a study of Abies religiosa. Wood samples were collected from 36 trees, grown between 3000 and 3500 masl, and then subjected to gravimetric and FTIR (Fourier Transform Infrared) spectroscopic analyses. The gravimetric results showed a proportion of 54.81 ± 2.20 % cellulose, 12.37 ± 1.33 % hemicellulose and 24.68 ± 1.16 % of insoluble lignin. Using the principal components analysis with analysis of variance (ANOVA), significant differences were found at 3100 and 3200 masl in two independent components related to both hemicellulose and lignin, through gravimetry as well as the spectroscopic bands assigned to the carbonyl groups of these polymers, respectively. However, the observed changes in chemical composition of LB did not follow a linear relationship with respect to the altitudinal gradient, which suggests that complex environmental interactions could also be playing an important role. Also, there were significant differences (p < 0.05) in two of the empirical indexes calculated from the FTIR analysis.     

Colorimetric and vibrational spectroscopic characterization of weathered surfaces of wood and rigid polyvinyl chloride–wood flour composite lumber

Rigid polyvinyl chloride–wood flour composite lumber containing either pine or maple wood flour and pine and maple lumber was subjected to accelerated weathering according to the ASTM Standard G 53 protocol. Non-weathered and weathered surfaces of all specimens were analyzed using colorimetric methods, reflectance infrared Fourier transform and Raman spectroscopic techniques. In the FT-IR spectra, conjugated ketones (1,744 cm^?1) of lignin as evidenced by their skeletal vibrations (1,560–1,500 cm^?1) and stretching (1,440–1,500 cm^?1) were reduced in weathered specimens. Cellulose was largely unaffected by weathering. C–O bending vibrations at 1,040 cm^?1 from holocellulose in pine specimens and intensity bands at 1,125–1,090 and 1,360 cm^?1 (C–O stretching and O–H bending from cellulose) in the maple and wood–plastic composite (WPC)-maple specimens were unaffected. A band at 1,650 cm^?1 became prominent after weathering of both pine and maple WPC specimens which is due to C=C–C=C stretching vibration of weathered PVC portion of the specimen. Raman shifts at 530 and 840–900 cm^?1 are attributed to C–O and C–C–O stretching in cellulose (remain unchanged). The role of extractives in weathering of pine is shown by the disappearance of Raman shifts at 392 and 434 cm^?1 (C=C deformations in pine extractives) in weathered pine. One-Way ANOVA, between-group designs showed significant effect on brightness (L*), redness (a*) and yellowness (b*) for all treatments.     

Physiological effects of touching hinoki cypress (<Emphasis Type="Italic">Chamaecyparis obtusa</Emphasis>)

This study aimed to clarify the physiological effects of touching hinoki cypress (hereinafter called “hinoki”) (Chamaecyparis obtusa) wood with the palm of the right hand on brain activity and autonomic nervous activity. Twenty-two female university students (mean age 21.1?±?0.2 years) participated in the study. As an indicator of brain activity, oxyhemoglobin (oxy-Hb) concentrations were measured in the left/right prefrontal cortex using near-infrared time-resolved spectroscopy. Heart rate variability (HRV) was used as an indicator of autonomic nervous activity. The high-frequency (HF) component of HRV, which reflected parasympathetic nervous activity, and the low-frequency (LF)/HF ratio, which reflected sympathetic nervous activity, were measured. Plate (300?×?300 mm) of uncoated hinoki was used as tactile stimulation. Marble was used as a control material. After sitting at rest with their eyes closed, the participants touched the materials for 90 s with their eyes still closed. The results showed that tactile stimulation with hinoki significantly decreased oxy-Hb concentration in the left prefrontal cortex and increased ln(HF) reflected parasympathetic nervous activity compared with marble. In conclusion, our study showed that touching hinoki wood with the palm calms prefrontal cortex activity and increases parasympathetic nervous activity, thereby inducing physiological relaxation.     

竹原纤维和竹粉纤维形态和化学成分分析

以3年生毛竹材为原料,研究了毛竹竹粉和竹原纤维的纤维形态和化学成分。纤维形态分析结果表明:竹原纤维的宽度(143μm)与竹粉(136μm)相当,长度(22.63 mm)远高于竹粉(0.61 mm),使其长宽比(158.25)远高于竹粉(4.49)。化学成分分析表明:竹原纤维的纤维素含量(65.6%)比竹粉(37.3%)高得多,聚戊糖含量(17.1%)略低于竹粉(20.1%)。竹粉中的木质素含量为24.5%,是竹原纤维中木质素含量(11.5%)的2倍多。竹原纤维的高纤维素含量和低木质素含量是其广泛应用于制浆造纸行业的重要原因。     

Quantifying lignin and holocellulose content in coniferous decayed wood using near-infrared reflectance spectroscopy

To determine the independent decomposition rates of lignin and cellulose of decayed woody debris, a technique for the rapid analysis of lignin and cellulose is required. We applied a near-infrared spectroscopy (NIRS) technique to measure the lignin and holocellulose content in decayed wood. We succeeded in creating partial least-squares (PLS) models to estimate the lignin and holocellulose content in the decayed wood of five species using NIR spectra. Although the accuracy was acceptable for the estimation of a five-species mixed model (R ² = 0.970 for lignin and R ² = 0.962 for holocellulose), it was further improved when the model was applied to each species independently. This combination of NIRS and a PLS model is a valuable tool for the determination of the lignin and holocellulose content in decayed wood. The technique is time efficient (3 min per sample) and non-hazardous (no acid treatment is required).     

竹浆纤维红外光谱分析及再生纤维素纤维市场简析

通过有效检测竹浆中的纤维素纤维的红外吸收光谱,并利用红外光谱仪等多种专业仪器来分析多种纤维素纤维的差别,可以得出纤维素纤维的结构差异性,从而有助于将其利用在工业化量产之后,结合其自身特性来区分应用方向。同时对再生纤维素纤维市场进行简析,为相关行业企业尽早做好应对贸易摩擦造成的负面影响准备提供参考。     

In vitro clonal propagation of Gardenia latifolia Ait.: a toy making woody tree

An efficient, in vitro clonal propagation protocol has been established for Gardenia latifolia Ait. using mature nodal explants on Murashige and Skoog (MS) medium fortified with cytokinins (BA/Kn/2-iP) (1.0–5.0 mg l^?1) in combination with auxin IAA (0.5 mg l^?1). Maximum bud break (87 %) with shoot number (7.2 ± 0.26) observed on MS medium supplemented with BA (4.0 mg l^?1) and IAA (0.5 mg l^?1). Maximum number of shoots (30 ± 0.46) with shoot length of (0.9 ± 0.03 cm) observed on MS medium supplemented with BA (2.0 mg l^?1), Kn (2.0 mg l^?1) and IAA (0.5 mg l^?1). Further elongation of shoots (3.5 ± 0.06 cm) was achieved on MS medium supplemented with BA (1.0 mg l^?1) and IAA (0.1 mg l^?1). About 70 % of root induction occurred in half-strength MS medium supplemented with IBA (4.0 mg l^?1) in 4–6 weeks. Further elongation of roots with average length (9.0 cm) was achieved in culture bottles containing vermiculite and ¼ strength MS salts. After their partial hardening in these bottles for 30 days they were transferred to pots containing a mixture of soil and vermicompost (1:1) for acclimatization. The acclimatized plantlets were established in the field successfully with 85 % survival rate.     

The effect of axial strain on crystalline cellulose in Norway spruce

The effect of strain on dry, clear Norway spruce (Picea abies [L.] Karst.) wood was studied by tensile testing along the cell axis and by in situ X-ray diffraction measurements. The mean microfibril angle (MFA) was initially 3–12 degrees and did not decrease due to strain. Based on the positions of the reflections 200 and 004 of crystalline cellulose, cellulose chains elongated and the distance between the hydrogen bonded sheets of chains decreased due to the strain. The elongation of the unit cell parallel to the cellulose chains was twice as high in juvenile wood as in mature wood. The (X-ray) Poisson ratio ν _ca for crystalline cellulose in Norway spruce was calculated from the deformation of the unit cell. The average ν _ca of earlywood was 0.28 ± 0.10 in juvenile wood and 0.38 ± 0.23 in mature wood. In latewood, the average ν _ca was 0.48 ± 0.10 in juvenile wood and 0.82 ± 0.11 in mature wood. The average ν _ca values were not directly correlated to the crystallite dimensions or to the mean MFA in juvenile and mature earlywood and latewood. The results show that the amorphous matrix has a definite effect on the deformation of cellulose crystallites.     

超声辅助提取对竹纤维结构和机械性能的影响

文章以超声波辅助提取竹纤维,研究超声波处理以及超声波处理方式（前超声和后超声）对低试剂量条件下提取竹纤维结构和热性能的影响。结果表明：超声波处理应用于低试剂量竹纤维提取,可降低竹纤维胶质含量,改善竹纤维细度和细度均匀性。用后超声辅助提取竹纤维,竹纤维胶质含量可降低13.2%,纤维直径由489±247 μm降至224±52 μm,平均直径降低率达54.2%。超声辅助提取对竹纤维机械性能有一定程度的影响,对竹纤维拉伸强度略有降低,拉伸模量下降明显,断裂伸长率略有提高,机械强度均匀性增加;后超声辅助提取较前超声辅助提取对竹纤维的机械性能降低程度小。经提取工艺,竹纤维结晶度增加,但超声辅助提取竹纤维结晶度又略有下降,未超声竹纤维结晶度为56.50%,后超声竹纤维结晶度为55.89%,前超声竹纤维结晶度为56.25%;傅里叶红外光谱分析表明,竹纤维化学结构变化主要由纤维提取工艺引起,超声处理对纤维结构影响不明显;通过电镜观察,经纤维提取工艺,原竹材结构中被胶质包覆的单纤维形态暴露,单丝状明显,超声辅助提取增加了纤维表面粗糙度,后超声辅助提取单丝分散性增强;总体上,超声辅助提取可促进低试剂量条件下的长竹纤维提取,对纤维细度有明显改善效果,但对纤维结构和机械性能影响不大。     

基于微波液化的木质纤维素组分分离和转化——纤维素组分的理化和酶解性质

【目的】将微波加热与甘油利用相结合的综合炼制工艺用于木质纤维素生物质预处理,探索其在燃料乙醇制备中的可行性,为实现经济可行、经济有效的木质纤维素生物质酶解预处理技术和生物燃料生产提供基础信息。【方法】以银腺杨、日本落叶松、刚竹和柳枝稷为试验材料,采用微波液化法对其进行液化处理,将液化产物分为纤维素、半纤维素和木质素组分,并对纤维素纤维组分进行综合表征。【结果】化学分析结果表明,纤维素纤维具有较高的葡聚糖含量;红外光谱显示,木质素和半纤维素的信号逐渐减弱,说明半纤维素和木质素经液化处理后有效脱除;XRD分析结果表明,纤维素纤维结晶度高、表面积大。【结论】相比原木质纤维素生物质,银腺杨、日本落叶松、刚竹和柳枝稷4种原材料纤维素纤维的酶解糖化效率均有不同程度提升(最高酶解转化率可达70%),液化固体产物--纤维素纤维在制备燃料乙醇中具有广阔的潜力和前景。     

Investigation of changes in compressed moso bamboo (<Emphasis Type="Italic">Phyllostachys pubescens</Emphasis>) after hot-press molding

In this study, molding moso bamboo strips to a curved shape using hot-press molding operation was explored. Bamboo strips with different thickness and moisture content (MC) were subjected to press molding under 120–210 °C for different time. Changes in the chemical components of bamboo were analyzed by Fourier-transform infrared spectroscopy (FTIR). Effect of MC on thermal mechanical behavior of bamboo was investigated using dynamic mechanical analysis (DMA). Results showed that the influencing degree of four variables on compression and recovery ratios decreased as: temperature?>?time?>?thickness?>?MC. Compression ratio increased and recovery ratio decreased dramatically when pressing temperature exceeded 180 °C. FTIR analysis indicated that polysaccharide (especially hemicelluloses) underwent a progressive thermal degradation during compression at 180 and 210 °C for 40 min, whereas relative content of lignin increased. DMA results showed that bamboo samples with a higher MC had a lower storage modulus value, confirmed water had a plasticizing effect. The loss factor of bamboo with higher MC (12 and 16%) exhibited two major transitions centred around 100 °C (α₁) and 50 °C (α₂), respectively. The temperature of these α transitions kept almost unchanged as moisture level increased from 12 to 16%. These findings provide fundamental information for the future preparation of curved bamboo as profiled components in engineered products.     

Micromorphological characteristics of bamboo (<Emphasis Type="Italic">Phyllostachys pubescens</Emphasis>) fibers degraded by a brown rot fungus (<Emphasis Type="Italic">Gloeophyllum trabeum</Emphasis>)

The decay pattern in bamboo fibers caused by a brown rot fungus, Gloeophyllum trabeum, was examined by microscopy. The inner part of the polylaminate secondary wall was degraded, while the outer part of the secondary wall remained essentially intact. Degradation in bamboo fiber walls without direct contact with the fungal hyphae was similar to wood decay caused by brown rot fungi. Degradation in polylaminate walls was almost confined to the broad layers whereas the narrow layers appeared resistant. The p-hydroxylphenyl unit lignin in middle lamella, particularly in the cell corner regions, was also degraded. The degradation of lignin in bamboo fibers was evidenced by Fourier transform infrared spectra. The present work suggests that the decay of bamboo fiber walls by G. trabeum was influenced by lignin distribution in the fiber walls as well as the polylaminate structures.