香蕉中噻唑膦残留分析方法研究

建立香蕉中噻唑膦的超高效液相色谱串联质谱法(UPLC-MS/MS)残留测定方法。香蕉样品采用乙腈提取和PSA+C18分散固相萃取,采用UPLC-MS/MS多反应模式(MRM)进行分析测定。噻唑膦在添加水平0.01~1.0 mg/kg范围内,平均回收率为94.3%~107.5%,相对标准偏差为7.9%~11.0%。采用外标法定量,方法的检出限为0.001μg/m L,定量限为0.005 mg/kg。该方法简单、准确、重复性较好且节省溶剂,适用于香蕉中噻唑膦的残留检测。     

甘蔗叶不同还田方式对土壤养分的影响

为减轻秸秆焚烧所带来的环境问题和充分利用甘蔗叶资源,在大田环境下动态监测甘蔗叶粉碎、焚烧和深埋3种还田方式对土壤养分的影响。结果表明:甘蔗叶粉碎还田和深埋还田有利于甘蔗叶中有机碳及氮、磷、钾养分的缓慢释放;甘蔗叶焚烧还田提高了土壤碱解氮含量5.6~20.9 mg/kg和速效磷含量0.8~4.0 mg/kg,促进土壤中氮磷向有效态转化,焚烧还田初期显著增加了土壤速效钾的含量12.3~18.3 mg/kg,但焚烧会损失部分甘蔗叶中碳氮元素,也造成环境污染。综合分析认为甘蔗叶粉碎还田是比较省工、方便的处理方式。     

抗白粉病胡麻种质资源田间鉴定与筛选

白粉病目前已成为影响胡麻产量和质量最常见的病害之一, 种植抗病品种是防控病害最经济环保的有效措施, 然而抗病亲本材料的缺乏已成为制约抗病品种选育的关键因素。为筛选出抗白粉病胡麻材料, 本研究在田间自然感病的条件下, 采用病情指数法对300份国内外胡麻种质资源材料进行了抗白粉病鉴定和评价。结果表明, 所有供试材料均程度不同地感染胡麻白粉病, 无免疫材料, 仅有5份材料为中抗; 其余295份均为感病材料, 其中8份材料中感, 52份材料感病, 235份材料高度感病。本研究可为抗白粉病胡麻品种的培育及相关抗病基因的发掘提供参考。     

GA4+7+氯吡脲对重瓣百合'Thalita'生长的影响

以重瓣百合'Thalita'为试材,采用4个不同浓度(10、20、40、80 mg·L-1)的GA4+7+氯吡脲(1∶1),对其进行叶面喷施处理,以清水为对照,测定其株高、茎粗、叶面积等指标,探讨GA4+7+氯吡脲对重瓣百合'Thalita'生长的影响,以期为其推广提供参考.结果 表明:20 mg·L-1 GA4+7+氯吡脲对'Thalita'花苞直径和叶面积促进作用最大,分别比对照高14.18％和55.13％,均达显著差异;茎粗随着GA4+7+氯吡脲的浓度升高表现出一定抑制作用;20 mg·L-1GA4+7+氯吡脲在花苞开放率和花期上综合效果最好;80 mg·L-1 GA4+7+氯吡脲对'Thalita'株高促进效果最好,比对照高2.67％;所有处理组种球鲜质量和根长均比对照低,其中20 mg·L-1 GA4+7+氯吡脲效果最为明显,分别比对照低36.77％和48.18％,均达显著差异.综合比较来看,20 mg·L-1 GA4+7+氯吡脲对重瓣百合'Thalita'生长影响最大,效果更佳.     

危害蒙古栎的新害虫——金纹吉丁

2018年在承德市双庙村蒙古栎林中发现吉丁幼虫危害现象,对其进行鉴定确定为金纹吉丁(Corebus aequalipennis Fairmaire),并对其分布范围、主要形态特征、生物学特性等进行了调查,提出了相应的防治措施。     

上海水稻精量机械穴直播技术研究与应用

以上海地区主推水稻品种为材料,在精量机械穴直播条件下,开展了不同类型水稻品种的小区试验和示范,明确了精量机械穴直播水稻的生育特性、抗倒伏性、群体建成和产量表现,并分析了采用水稻精量机械穴直播后土壤的微生物群落结构的变化和水稻生产经济效益。试验示范结果表明,精量机械穴直播水稻生育期明显缩短,单株分蘖力强,群体结构合理,穗粒结构协调,干物质积累多,抗倒能力较强,增产优势明显,节本低耗,生产效率显著提高,是目前极具生产潜力的一种新型高效低耗种植模式,适合上海都市农业发展的需求,也顺应了水稻低碳种植发展趋势,具有广阔的应用前景。     

MicroRNA-145 inhibits epithelial-mesenchymal transition in human renal cancer A-498 cells by ADAM28

AIM: To investigate the inhibitory effect of microRNA-145 (miR-145) on epithelial-mesenchymal transition (EMT) in renal cancer A-498 cells. METHODS: The A-498 cells were transfected with miR-145 mimics (M145) and mimic negative control(MNC), which served as M145 group and MNC group, respectively. Mock control (MC) group was set up using untreated A-498 cells. The expression level of miR-145 in each group was detected by RT-qPCR. Transwell assay was used to detect the invasion ability of the cells. The protein expression of vimentin, E-cadherin and ADAM28 was determined by Western blot. Bioinformatic method was used to predict the target genes of miR-145. Antagonistic effect of ADAM28 over-expression on the inhibition of EMT by miR-145 was detected by Western blot. The relationship between miR-145 and ADAM28 was analyzed by dual-luciferase reporter assay. RESULTS: The expression level of miR-145 in M145 group was significantly up-regulated than that in MC group (P<0.05). The number of invasive cells in M145 group was 12.78±3.37, which was significantly lower than that in MC group (P<0.05). ADAM28 may be the target gene of miR-145. Compared with MC group, the protein expression of vimentin and ADAM28 in M145 group was significantly decreased (P<0.05), while the protein expression of E-cadherin was significantly increased (P<0.05).After ADAM28 over-expression, the protein expression of vimentin in the A-498 cells of M145 group was significantly increased (P<0.05), and the protein expression of E-cadherin was significantly decreased (P<0.05). The results of dual-lucife-irasei reporter assay showed that ADAM28 was a downstream target gene of miR-145. CONCLUSION: miR-145 may inhibit the expression of EMT-related proteins through the downstream target gene ADAM28 and inhibit the EMT process of renal cancer A-498 cells.     

Effect of dietary calcium or phosphorus deficiency on bone development and related calcium or phosphorus metabolic utilization parameters of broilers from 22 to 42 days of age

This experiment was conducted to investigate the effect of dietary calcium (Ca) or phosphorus (P) deficiency on bone development and related Ca or P metabolic utilization parameters of broilers from 22 to 42 days of age based on our previous study, which indicated that dietary Ca or P deficiency impaired the bone development by regulating related Ca or P metabolic utilization parameters of broilers from 1 to 21 days of age. A total of 504 one-day-old Arbor Acres male broilers were randomly assigned to 1 of 4 treatments with 7 replicates in a completely randomized design, and fed the normal control and Ca- or P-deficient diets from 1 to 21 days of age. At 22 days of age, the broilers were further fed the normal control diet (0.90% Ca+0.35% non-phytate P (NPP)), the P-deficient diet (0.90% Ca+0.18% NPP), the Ca-deficient diet (0.30% Ca+0.35% NPP) or the Ca and P-deficient diet (0.30% Ca+0.18% NPP), respectively. The results showed that dietary Ca or P deficiency decreased (P<0.05) tibia bone mineral density (BMD), bone breaking strength (BBS), ash content, tibia ash Ca content and serum P content on days 28 and 42, but increased (P<0.05) tibia alkaline phosphatase (ALP) activity of broilers on day 42 compared with the control group. Furthermore, the broilers fed the P-deficient diet had the lowest (P<0.05) tibia BMD, BBS, ash content, serum P content and the highest (P<0.05) serum Ca content on day 28 compared with those fed the Ca-deficient or Ca and P-deficient diets. The results from the present study indicated that the bone development and related Ca or P metabolic utilization parameters of broilers were the most sensitive to dietary P deficiency, followed by dietary Ca deficiency or Ca and P-deficiency; dietary Ca or P deficiency impaired the bone development possibly by regulating serum Ca and P contents as well as tibia Ca content and ALP activity of broilers from 22 to 42 days of age.     

养殖密度对硝化型生物絮团系统中凡纳滨对虾生长和水质的影响

利用硝化型生物絮团系统进行凡纳滨对虾的养殖,并通过设置不同的养殖密度探究不同养殖密度下硝化型生物絮团系统对凡纳滨对虾生长性能和水质情况的影响。实验选择同一批标粗到一定规格的健康凡纳滨对虾[体长(4.80±0.25) cm,体质量(0.98±0.16)g],分成5个密度梯度组放养到养殖池中,进行为期45 d的养殖。结果表明:80～610尾/m~3范围内,硝化型生物絮团系统对非离子氨和亚硝酸盐氮可以控制在警戒浓度(0.2 mg/L)附近波动,为凡纳滨对虾健康生长提供了良好的环境,保证养殖存活率,另外该系统下适当的排污可以避免高密度养殖下硝酸盐氮积累太快;80～610尾/m~3时存活率随密度升高而下降,但产量随密度升高而增加。