温室环境控制方法研究现状分析与展望

环境控制方法是实现温室蔬菜高效生产的关键。随着现代控制技术的快速发展,温室环境控制方法逐步从手动、定时控制方法,转变为设定值控制和智能控制等方式。该文概述了以设定值为目标实现环境控制的方法,归纳了模糊控制、解耦控制、人工智能控制和表型控制等智能控制方法的特点,总结了现有温室环境调控领域控光、控温、控气、通风、灌溉和“云-边-端”协同控制系统的优劣。针对现存问题,指出该领域的发展趋势为构建考虑扰动因素影响的温室环境控制方法,研制基于作物生长和表型评价体系的环境调控模型,以及建立多模型融合的“云-边-端”协同温室环境调控系统。相关技术的发展将为温室的智能化与信息化发展提供重要的决策依据和借鉴意义。     

微粒体甘油三酯转运蛋白研究进展

从微粒体甘油三酯转运蛋白(MTP)结构、功能、活性与多态性、脂代谢中的作用、表达与调节等方面综述了微粒体甘油三酯转运蛋白是一种重要的脂质转运蛋白,着重论述了MTP与脂代谢关系、MTP表达与调节.MTP的活性、基因表达状态是控制极低密度脂蛋白合成、装配和分泌速率的重要因素,研究MTP基因表达与调节对预防动物脂肪肝、提高畜禽生产品质,探讨人类脂类代谢性疾病和心血管疾病等重要疾病形成机制,对防治这些疾病具有重要的临床意义.     

微生物发酵豆粕对断奶仔猪生长、血清指标及肠道形态的影响

本文旨在研究微生物发酵豆粕对仔猪生长及血清指标的影响,并且根据肠道组织形态学的微观变化,评价了不同处理的豆粕对早期断奶仔猪肠道形态的影响.选用60头35日龄断奶体重为(8.62±0.21)kg的同窝杜×长×大仔猪,分为试验组和对照组,每组3个重复,每个重复10头,分别饲喂以普通豆粕为对照组,微生物发酵豆粕为试验组的日粮.试验结果表明:饲喂微生物发酵豆粕使仔猪料重比降低8.39%(P＜0.05),腹泻指数降低39.96%(P＜0.01),血清尿素氮含量降低39.47%(P＜0.01),血清IgG含量降低6.35%(P＜0.05).豆粕经微生物发酵后减轻饲粮中大豆蛋白对肠道的过敏损伤,使肠道维持良好的结构形态,从而促进营养物质的消化吸收.     

黄河干流梯级水库补偿调节方案风险分析

本文以黄河干流梯级水库补偿调节为例,系统分析了补偿调节方案的主要风险因素,提出了多因素组合风险估计的蒙特卡罗(Monte-Carlo)随机模拟技术,并根据风险指标对补偿调节方案的风险做出评价。结果表明,研究建立的补偿调节方案风险模型是合理可行的。     

Effects of Photoperiod on Stem Cells Activation in Cashmere Goat Hair Follicles

In order to extend the anagen of cashmere goat hair follicles and increase the production of cashmere,this study was performed with artificially shorten the daylight time among Arbas White cashmere goats. Skin tissue sections from cashmere goats were collected to compare the morphologic changes between artificial daylight and natural daylight,and immunohistochemical method was used to study the hair follicle cell proliferation and important protein expression in related signaling pathways. The results showed that strong cell proliferation occurred in cashmere goat hair follicle cells during artificial daylight,plenty of cytokeratin 15 (K15) positive signals were distributed in the outer root sheath,β-catenin protein was actively expressed in hair matrix and root sheath, indicating that the hair follicles were in the anagen growth phase;Meanwhile,cashmere goat hair follicles under natural daylight were in telogen with weak signals. Above all prove that short photoperiod played an important role in promoting hair follicle growth,the artificial short photoperiod could change hair follicle growth cycle and make hair follicles earlier enter to the anagen growth phase,causing a variety of typical gene expressions during hair follicle growth.     

硒蛋白的基因表达与调控

硒蛋白是微量元素硒以硒代半胱氯酸(SeC)形式进入多肽链的蛋白质。SeC的遗传密码是UGA。在原核细胞中,4种基因产物SELA、SELB、SELC和SELD参与了硒蛋白的合成过程。真核生物硒蛋白mRNA3’-UTR的硒代半胱氨酸插入序列(SECIS)是真核细胞UGA密码编码SeC的顺式作用元件。动物的硒营养状态不影响硒蛋白基因的转录,但影响硒蛋白mRNA的稳定性。饲料硒水平与含硒酶活性呈正相关。     

安徽白山羊杂交效应

对安徽白山羊及其二元杂交组合(波×安,萨×安)、三元杂交组合(波×萨×安,马×萨×安)和级进杂交组合(波×波×安)研究表明:(1)杂交能提高安徽白山羊的生长发育速度。二元杂交和三元杂交组合在6月龄前生长较快,6月龄后变慢;级进杂交在8月龄前生长较快。(2)无论是二元杂交还是三元杂交,均能提高安徽白山羊的产肉性能(P<0 01,P<0 05),但肉质有下降的趋势,三元杂交比二元杂交下降更多。(3)二元杂交和三元杂交能够增大安徽白山羊板皮面积(P<0 01,P<0 05),减小毛纤维密度,二元杂交使板皮的均匀度提高。     

Estrogen suppresses melatonin-enhanced hyperactivation of hamster spermatozoa

Hamster sperm hyperactivation is enhanced by progesterone, and this progesterone-enhanced hyperactivation is suppressed by 17β-estradiol (17βE₂) and γ-aminobutyric acid (GABA). Although it has been indicated that melatonin also enhances hyperactivation, it is unknown whether melatonin-enhanced hyperactivation is also suppressed by 17βE₂ and GABA. In the present study, melatonin-enhanced hyperactivation was significantly suppressed by 17βE₂ but not by GABA. Moreover, suppression of melatonin-enhanced hyperactivation by 17βE₂ occurred through non-genomic regulation via the estrogen receptor (ER). These results suggest that enhancement of hyperactivation is regulated by melatonin and 17βE₂ through non-genomic regulation.     

NPFFR1基因对鹅卵泡颗粒细胞激素分泌和细胞凋亡的影响研究

神经相关肽受体（RFamide-related peptide receptor,NPFFR1）是促性腺激素抑制激素的主要亲和受体,它在调控动物繁殖方面起着重要作用。为了解NPFFR1对鹅卵巢卵泡发育的作用,本研究以42周龄健康产蛋四川白鹅为试验材料（n=9）,利用RT-qPCR法检测NPFFR1基因在等级前和等级卵泡颗粒细胞中的mRNA表达规律;在颗粒细胞中过表达NPFFR1基因,酶联免疫吸附法检测颗粒细胞上清液（n=9）中雌二醇（estradiol,E2）、孕酮（progesterone,P4）和抗缪勒管激素（anti-Mullerian hormone,AMH）的浓度变化,剩余贴壁细胞作一步法TUNEL检测细胞凋亡情况;转录组测序方法筛选大黄卵泡（8~10 mm）颗粒细胞过表达NPFFR1前后表达差异显著基因,并对差异表达基因进行功能聚类分析。结果显示,除F1等级外,其余等级卵泡颗粒细胞NPFFR1表达量均极显著高于等级前卵泡（P<0.01）;过表达NPFFR1后,等级颗粒细胞上清液中的E2和等级前颗粒细胞上清液AMH的含量显著（P<0.05）降低,但孕酮P4含量变化不显著（P>0.05）;转录组测序共筛选到267个差异表达基因（119个下调,148个上调）,这些基因主要富集在生物节律过程、繁殖进程等生物学过程中;同时,与对照组相比,差异基因AMH显著下调表达（P<0.05）,Clock（clock circadian regulator）、FOS（proto-oncogene,AP-1 trans-cription factor subunit）、Per（period circadian regulator）和ANTXR2（cell adhesion molecule 2）分别极显著（P<0.01）或显著（P<0.05）上调表达。上述试验结果提示,NPFFR1可从激素、细胞凋亡和生物节律等多个环节影响卵泡颗粒细胞,参与调控卵泡的时序等级发育。     

Fluazifop-butyl causes membrane peroxidation in the herbicide-susceptible broad leaf weed bristly starbur (Acanthospermum hispidum)

In order to clarify the action mechanism of fluazifop-butyl, an aryloxyphenoxypropionate (AOPP) herbicide in bristly starbur (Acanthospermum hispidum DC.), a unique fluazifop-butyl-susceptible broad-leaved weed, ethylene evolution and membrane lipid peroxidation in the plant seedlings were investigated. Foliar application of fluazifop-P-butyl induced ethylene evolution only from bristly starbur, but not from oat (Avena sativa L.), another fluazifop-butyl-susceptible species, and two tolerant species, pea (Pisum sativum L.) and hairy beggarticks (Bidens pilosa L.). The other AOPP herbicides, quizalofop-ethyl and fenoxaprop-ethyl, and a cyclohexanedione (CHD) herbicide, sethoxydim, did not enhance ethylene production from bristly starbur. This fluazifop-butyl-induced ethylene production in bristly starbur was completely suppressed by aminoethoxyvinylglycine (AVG), a 1-aminocyclopropane-1-carboxylic acid (ACC) synthase inhibitor, but not by p-chlorophenoxyisobutyric acid (PCIB), an anti-auxin compound, suggesting this evolved ethylene was not auxin-induced. Phytotoxic action by fluazifop-P-butyl (5 μM) in bristly starbur was reduced markedly by two lipid-soluble antioxidants, vitamin E, and ethoxyquin. The ethylene production from the plant was also inhibited by these two antioxidants. Content of malondialdehyde, an indicator of lipid peroxidation, increased only by fluazifop-P-butyl in bristly starbur seedlings but not in oat, and this increase was inhibited by ethoxyquin. These results strongly suggest that the primary site of action for fluazifop-butyl in bristly starbur is on the membranes and active oxygen species and/or free radicals are involved in peroxidation. Ethylene evolution is probably induced by these reactive oxygen species.