Silver catfish Rhamdia quelen immersion anaesthesia with essential oil of Aloysia triphylla (L'Hérit) Britton or tricaine methanesulfonate: effect on stress response and antioxidant status

Responses to anaesthesia with essential oil (EO) of Aloysia triphylla (135 and 180 mg L^?1) and tricaine methanesulfonate (MS222) (150 and 300 mg L^?1) were assessed in silver catfish. Exposure to the anaesthetics elicited a stress response in the species. In the case of MS222, it was displayed as a release of cortisol into bloodstream, elevation in hematocrit and plasma ion loss. The EO presented cortisol‐blocking properties, but increased haematocrit and disturbances of hydromineral balance were observed. Liver antioxidant/oxidant status of EO and MS222‐anaesthetized silver catfish was also estimated. The synthetic anaesthetic induced lipoperoxidation, notwithstanding increased catalase contents, whereas the naturally occurring product was capable of preventing the formation of lipid peroxides, possibly due to combined actions of catalase and glutathione‐S‐transferase. Anaesthetic efficacy was also tested via induction and recovery times. Overall, the promising results obtained for the physiological parameters of the EO‐treated fish counterbalanced the slight prolonged induction time observed for 180 mg L^?1. As for 135 mg L^?1, both induction and recovery times were lengthy; despite that, the EO was able to promote oxidative protection and mitigate stress. None of the MS222 concentrations prompted such responses concomitantly.     

Effects of Protease and Urea on a Granular Starch Hydrolyzing Process for Corn Ethanol Production

The dry grind process using granular starch hydrolyzing enzymes (GSHE) saves energy. The amount of GSHE used is an important factor affecting dry grind process economics. Proteases can weaken protein matrix to aid starch release and may reduce GSHE doses. Two specific proteases, an exoprotease and an endoprotease, were evaluated in the dry grind process using GSHE (GSH process). The effect of protease and urea addition on GSH process was also evaluated. Addition of these proteases resulted in higher ethanol concentrations (mean increase of 0.3–1.8 v/v) and lower distillers' dried grains with solubles (DDGS) yields (mean decrease of 1.3–8.0% db) compared with the control (no protease addition). As protease levels and GSHE increased, ethanol concentrations increased and DDGS yields decreased. Protease addition reduced the required GSHE dose. Final mean ethanol concentrations without urea (15.2% v/v) were higher than with urea (15.0% v/v) in GSH process across all protease treatments.     

PCR-sequence characterization of new adenoviruses found in reptiles and the first successful isolation of a lizard adenovirus

A consensus nested PCR was used to screen diagnostic samples from approximately 70 reptiles for the presence of adenoviruses (AdV) in the years 2006-2007. Classical virus isolation methods were also used with all samples. After adenoviruses were detected in a group of helodermatid lizards in a Danish zoo, a follow-up study was also carried out on lizards from this group (10 Mexican beaded lizards and 24 Gila monsters) over the period of a year. Adenoviruses were detected in a total of 26 lizards and snakes by PCR. The PCR amplicons from all positive animals were sequenced and the resulting polymerase gene sequences were used for phylogenetic analysis. Altogether six Agamid AdVs were amplified, with a minimal sequence variation between one another and between these and GenBank Agamid AdVs. The sequence obtained from one of the Gila monsters is identical with the GenBank Helodermatid AdV, while the sequences from the Mexican beaded lizards differ from this. In a snake collection we have detected a new AdV from an Asp viper. All of the above mentioned adenoviruses cluster in the Atadenovirus genus. However, the sequence from a new Varanid AdV detected in this study clusters outside this genus. On cell culture, viruses were isolated from three of the AdV positive helodermatid lizards (one Mexican beaded lizard and two Gila monsters) and identified as AdVs based on electron microscopy and PCR and sequencing using cell culture supernatant. This is the first report of the successful isolation of a lizard AdV.     

A method to generate soilscapes from soil maps

Digital soil mapping for large areas is challenging if mapping resolution should be as high as possible and sampling should be as sparse as possible. Generally, the more complex the soil associations in a landscape, the more samples are required to systematically cover the entire feature space. Moreover, regions should be modeled separately if the patterns of spatial variation vary on subregion level. A systematic segmentation of a landscape into soilscapes is additionally important for a feasible application of soil‐sensing approaches. In this paper, we introduce a semiautomated approach to segment nominal spatial datasets based on the local spatial frequency distribution of the mapping units. The aim is to provide homogeneous and nonfragmented segments with smoothed boundaries. The methodological framework for the segmentation comprises different spatial and nonspatial techniques and focuses mainly on a moving‐window analysis of the local frequency distribution and a k‐means cluster analysis. Based on an existing soil map (1:50,000), we derived six segments for the Nidda catchment (Central Hesse, Germany), comprising 1600 km². As segmentation is based on a soil map, soilscapes are derived. In terms of the feature space, these soilscapes show a higher homogeneity compared to the entire landscape. Advantages compared to an existing map of landscape units are discussed. Segmenting a landscape as introduced in this study might also be of importance for other disciplines and can be used as a first step in biodiversity analysis or setting up environmental‐monitoring sites.     

Fast molecular detection of Pseudomonas syringae pv. aesculi in diseased horse chestnut trees

A molecular technique was used to detect the bacterium Pseudomonas syringae pv. aesculi in horse chestnut trees (Aesculus hippocastanum), affected by the recently recognized European ‘Pseudomonas horse chestnut bark disease’. The technique helped identify the pathogen within 6 h of sample preparation including DNA extraction, polymerase chain reaction (PCR) and electrophoresis until gel documentation. PCR primer pairs derived from the gyrase B gene sequence were used. Because of the great similarity in the gyrase B gene sequences of the numerous closely related P. syringae pathovars, the primers were not only totally specific to the pathovar aesculi, but also detected a few other pathovars. The assumption that other bacteria should not occur at least near to a necrotic lesion of a horse chestnut tree was corroborated by sequence identity of the PCR products obtained with the gyrase B gene sequence of P. syringae pv. aesculi. Koch’s postulates were fulfilled for an isolate of P. syringae pv. aesculi obtained from a diseased horse chestnut tree sampled in Hamburg in 2007.     

竹类对真菌的感受性

本文对来自几个不同国家竹类茎秆的霉菌和担子菌进行分离和DNA测序鉴定。对蓝变真菌的纯培养的样品的实验室染色试验表明,正如发生在木材细胞组织中的一样,密集的褐变菌丝、厚垣孢子对组织的侵染和木质化细胞壁的渗透压扭作用。利用不同的测试安排的纯培养的白变、褐变和软腐真菌的退化实验表明,相当大的质量损失是由于白化菌和软腐菌引起的。本研究通过透射电镜证实了真菌攻击的微观形态学表现。研究结果改变了真菌破坏竹子的基本看法,需要改进竹资源更好利用和更适当保护的措施。     

Improving in-season nitrogen recommendations for maize using an active sensor

An active crop canopy reflectance sensor could be used to increase N-use efficiency in maize (Zea mays L.), if temporal and spatial variability in soil N availability and plant demand are adequately accounted for with an in-season N application. Our objective was to evaluate the success of using an active canopy sensor for developing maize N recommendations. This study was conducted in 21 farmers’ fields from 2007 to 2009, representing the maize production regions of east central and southeastern Pennsylvania, USA. Four blocks at each site included seven sidedress N rates (0–280 kg N ha⁻¹) and one at-planting N rate of 280 kg N ha⁻¹. Canopy reflectance in the 590 nm and 880 nm wavelengths, soil samples, chlorophyll meter (SPAD) measurements and above-ground biomass were collected at the 6th–7th-leaf growth stage (V6–V7). Relative amber normalized difference vegetative index (ANDVI_relative) and relative SPAD (SPAD_relative) were determined based on the relative measurements from the zero sidedress treatment to the 280 kg N ha⁻¹ at-planting treatment. Observations from the current study were compared to relationships between economic optimum N rate (EONR) and ANDVI_relative, presidedress NO₃ test (PSNT), or SPAD_relative that were developed from a previous study. These comparisons were based on an absolute mean difference (AMD) between observed EONR and the previously determined predicted relationships. The AMD for the relationship between EONR and ANDVI_relative in the current study was 46 kg N ha⁻¹. Neither the PSNT (AMD = 66 kg N ha⁻¹) nor the SPAD_relative (AMD = 72 kg N ha⁻¹) provided as good an indicator of EONR. When using all the observations from the two studies for the relationships between EONR and the various measurements, ANDVI_relative (R² = 0.65) provided a better estimate of EONR than PSNT (R² = 0.49) or SPAD_relative (not significant). Crop reflectance captured similar information as the PSNT and SPAD_relative, as reflected in strong relationships (R² > 0.60) among these variables. Crop canopy reflectance using an active sensor (i.e. ANDVI_relative) provided as good or better an indicator of EONR than PSNT or SPAD_relative, and provides an opportunity to easily adjust in-season N applications spatially.     

Effect of different dietary ratios of sunflower and linseed oils on growth and carcass traits of rabbits

As part of an experiment aiming to modify the meat fatty acid profile, this work studied the growth and carcass traits as affected by various dietary ratios of sunflower oil and linseed oil. A diet without added oil served as a control (C). Four other diets were equally 4% oil-enriched but they differed in the incorporation ratios of sunflower oil (S) to linseed oil (L), i.e. 4% S to 0% L (diet 4%S), 3% S to 1% L (diet 3:1%SL), 2% S to 2% L (diet 2:2%SL) and 0% S to 4% L (diet 4%L). The oil-rich diets had slightly higher digestible energy contents (11.4 vs 10.6 MJ/kg) than the C feed. In each group 10 litters of 7 to 9 Pannon White kits per litter were studied in the pre-weaning period from 21 to 35 days old. Growth and slaughter traits were assessed with 50 and 30 rabbits per group, respectively. No significant effects of diets were found on litter and doe performances. The only significant differences in growth performance of the C, 4%S, 3:1%SL, 2:2%SL and 4%L rabbits were for the 35–49 day feed intake (88, 86, 84, 84 and 83 g per day, respectively, P = 0.046), the 35–84 day growth rate (36, 38, 37, 35 and 37 g/day, P = 0.034) and the 84-day body weight (2608, 2703, 2664, 2565 and 2628 g, respectively, P = 0.022). There were several significant differences in carcass traits including the weight of reference carcass (1357, 1391, 1388, 1380 and 1369 g, respectively, P = 0.004) and left longisimus dorsi meat (78, 79, 81, 81 and 76 g, respectively, P = 0.046) of rabbits. The diets had major effects on the L*, a* and b* colour values (lightness, redness and yellowness) of meat and fat. Carcass colour of the C and 4%S rabbits was closer and the 4%L rabbits was further from the European consumer's preference of light coloured, less red and slightly yellow rabbit meat. Our result reveals the importance of age and body weight at slaughter. Taking the growth and slaughter performances and, the recent belief of human health benefits from lower n− 6/n− 3 FAs dietary ratios into account, the 2:2%SL diet seems most appropriate if the interests of the raisers, meat processors and buyers are considered equally.