基于经济效益的农业新型经营主体小麦玉米全程机械化农机配备研究

因山东省旱作灌溉区种植模式多样、技术模式不统一，规模化生产下的机械效能未能充分发挥，存在动力机械与机具配套比低、农机动力与资金浪费问题，在对小麦玉米周年轮作下全程机械化技术模式调研后，总结小麦玉米全程机械化技术路线，构建以作业成本最小为目标的农机装备优化配备模型。通过对平度市某小麦玉米种植合作社进行计算，作业成本较实际情况下降10.9%；总动力优化配备结果为23.712 kW，下降51.36%；农机配套比提高50%。研究结果可为山东省旱作灌溉区小麦玉米全程机械化技术模式优选、农机农艺深度融合、农业合作社的农机配备等方面提供技术参考。     

小麦4B染色体上LOX基因的等位变异及其区域分布

为了解中国不同麦区小麦种质资源籽粒脂肪氧化酶（lipoxygenase,LOX）活性相关基因TaLox-B1的差异和分布,利用小麦4B染色体上的功能标记LOX16和LOX18对7个麦区的436份种质资源进行分子检测。结果表明：在供试材料中共检测到3种TaLox-B1基因等位变异类型,分别为TaLox-B1a（与高LOX活性相关)、TaLox-B1b（与低LOX活性相关）和杂合型,其频率分别为19.0％、70.4％和10.6％。小麦LOX活性基因不同变异类型在各生态区的分布存在明显差异：基因型TaLox-B1a在黄淮冬麦区、北部冬麦区和长江中下游冬麦区分布较多,其比例分别为21.1%、19.8%和17.6%;基因型TaLox-B1b在西南冬麦区和长江中下游冬麦区分布较多,比例分别为87.9%、72.5%;杂合型仅存在于北部冬麦区、黄淮冬麦区与长江中下游冬麦区,比例分别为14.2%、12.4%和9.8%。利用标记LOX16和LOX18对53个自选高代品系进行分子检测,发现自选品系仅有TaLox-B1b与杂合型两种基因型,其中基因型TaLox-B1ab有32个,比例为60.4%。采用分子标记辅助选择,有利于快速鉴定小麦籽粒LOX活性,加速LOX的遗传改良和新品种选育。     

‘哈伯’南天竹组织培养和快速繁殖

为建立‘哈伯’南天竹组织培养和种苗繁育技术体系,以半木质化带芽茎段为外植体材料开展植株再生研究。通过观察对比试验法、L₉(3⁴)正交试验设计完全随机法、极差分析、显著性检验、LSD多重比较,探讨了‘哈伯’南天竹组培的最适培养基配方。试验结果表明：最佳诱导培养基为MS + 6-BA 2.0 mg/L + IBA 0.1 mg/L +蔗糖30 g/L,诱导萌动率71.77%,成活率85.51%;最佳增殖培养基为WPM +6-BA 1.5 mg/L + IBA 0.01 mg/L + 蔗糖30 g/L,增殖系数6.3;最佳生根培养基为1/2 MS+ IBA 0.5 mg/L + NAA 1.0 mg/L + 蔗糖20 g/L + AC 0.2 g/L,生根率97.63%;试管苗移入泥炭土:珍珠岩=3:2(V/V)混合基质中,移栽成活率96.67%。该试验建立了高效稳定的组培快繁技术体系,得到的组培苗后代能够稳定的保持母本优良性状,为工厂化育苗提供了技术支撑。     

滴灌下生物质改良材料对盐渍土水盐氮运移的调控效应

为探究生物质改良材料对滴灌盐渍土水、盐、肥运移过程的调控效应，采用土箱模拟试验，研究了水肥一体化滴灌条件下，生物炭和腐殖酸两种改良材料对盐渍土水、盐、氮运移和再分布过程及其时空分布特征的影响规律。结果表明：在滴灌条件下，盐渍土壤水盐的时空动态变化表现出明显的水分入渗驱动的盐分运移过程和蒸发扩散驱动的水盐再分布过程；铵态氮含量在时间上表现出先增大、后减小的变化趋势，在空间上的运移再分布特征较弱；硝态氮含量初始时空分布表现出与水盐相似的运移特征，受铵态氮硝化作用的多重影响，后期空间分布与铵态氮空间分布相似；生物炭通过提高土壤饱和导水率，增大了入渗阶段土壤水、盐、氮的运移速率和分布范围；腐殖酸通过提高土壤田间持水率增大了再分布过程土壤水、盐、氮的分布范围和强度，同时其对尿素的水解和硝化过程表现出更强的抑制效果。应用生物质改良材料在改变土壤物理性状进而调控滴灌土壤水盐运移的同时，还影响土壤氮素转化运移过程及其分布，这为水肥一体化滴灌盐渍农田的节水、控盐、减肥治理提供了理论基础。     

氮磷钾配比对长优2号产量和经济性状的影响

采用“3414”方案设计试验,研究氮磷钾不同配比施肥对长优2号产量及经济性状的影响,结果表明,氮、磷、钾对长优2号都有一定的增产效应,其中以氮的增产效应最为显著,磷与钾次之。初步得出本次试验最佳施肥量为“N”16.23㎏/667㎡、“P2O5”8.46㎏/667㎡、“K2O”16.06㎏/667㎡,NPK比接近“1：0.5：1”水平。     

利用KASP标记定位小麦群体中的无芒位点Awn-4A.1

芒是小麦穗部重要的光合器官之一，是小麦长期进化和适应环境的产物，对小麦产量和逆境适应具有重要影响。为了探究芒的发育及芒长的遗传机制，本研究利用小麦无芒品种中国春（Chinese Spring，CS）和有芒品系MK147构建的F₂分离群体与F₅代重组自交系（RIL）群体为材料，对无芒位点进行了标记和定位。遗传分析表明，群体中的无芒性状受半显性单基因控制；采用Wheat660K SNP芯片结合集群分离分析法（bulked segregate analysis，BSA）在F₂群体构建的无芒、有芒混池中检测到一个多态性SNP标记的富集区，初步将QTL定位于4A染色体上。在该QTL区间开发了58个KASP标记，并将定位区间缩小至KASP标记SNP-1537与SNP-4195之间，遗传距离为0.81 cM，对应中国春参考基因组（IWGSC.Ref.V1.0）4A染色体上9.23 Mb （100.56～109.79 Mb）的区间，将该位点命名为 Awn-4A.1。     

天津春稻和麦茬稻品质特性比较

以天津市培育的优质小站稻品种津川1号和隆优619为供试材料,分析了春稻和麦茬稻品质特性的差异。结果表明,津川1号作麦茬稻的整精米率明显低于作春稻,而垩白粒率显著高于春稻;津川1号麦茬稻的蛋白质含量明显偏高,食味值显著低于春稻;隆优619作春稻和麦茬稻无论在外观、加工、食味还是营养品质方面均无显著差异,是较理想的麦茬连作品种。     

马铃薯枯萎病和干腐病药剂防治筛选试验报告

马铃薯产业是宁夏“1+4”特色优势产业,是西吉县所有农作物中种植面积最大、涉及农户最多、比较效益最高的农民脱贫致富的主导产业。近年来西吉县马铃薯产业由商品薯种植大县向种薯繁育大县的转变,推动了农业增效,农民增收的快速发展。但各类土传性病害的发生影响了马铃薯产业的发展,同时磋商了农民种植的积极性。为了测定筛选出对马铃薯枯萎病和干腐病防治效果好、成本较低药剂,为大田防治提供科学依据。     

Exogenous application of allelopathic water extracts helps improving tolerance against terminal heat and drought stresses in bread wheat (Triticum aestivum L. Em. Thell.)

The allelopathic water extracts (AWEs) may help improve the tolerance of crop plants against abiotic stresses owing to the presence of the secondary metabolites (i.e., allelochemicals). We conducted four independent experiments to evaluate the influence of exogenous application of AWEs (applied through seed priming or foliage spray) in improving the terminal heat and drought tolerance in bread wheat. In all the experiments, two wheat cultivars, viz. Mairaj‐2008 (drought and heat tolerant) and Faisalabad‐2008 (drought and heat sensitive), were raised in pots. Both wheat cultivars were raised under ambient conditions in the wire house till leaf boot stage (booting) by maintaining the pots at 75% water‐holding capacity (WHC). Then, managed drought and heat stresses were imposed by maintaining the pots at 35% WHC, or shifting the pots inside the glass canopies (at 75% WHC), at booting, anthesis and the grain filling stages. Drought stress reduced the grain yield of wheat by 39%–49%. Foliar application of AWEs improved the grain yield of wheat by 26%–31%, while seed priming with AWEs improved the grain yield by 18%–26%, respectively, than drought stress. Terminal heat stress reduced the grain yield of wheat by 38%. Seed priming with AWEs improved the grain yield by 21%–27%; while foliar application of AWEs improved the grain yield by 25%–29% than the heat stress treatment. In conclusion, the exogenous application of AWEs improved the stay green, accumulation of proline, soluble phenolics and glycine betaine, which helped to stabilize the biological membranes and improved the tolerance against terminal drought and heat stresses.     

Replication of neurovirulent equine herpesvirus type 1 (EHV-1) in CD172a+ monocytic cells

Equine herpesvirus type 1 (EHV-1) is responsible for respiratory disorders, abortion and myeloencephalopathy (EHM) in horses. Two pathotypes of EHV-1 strains are circulating in the field: neurovirulent (N) and non-neurovirulent (NN). For both strains, CD172a⁺ monocytic cells are one of the main carrier cells of EHV-1 during primary infection, allowing the virus to invade the horse’s body. Recently, we showed that EHV-1 NN strains showed a restricted and delayed replication in CD172a⁺ cells. Here we characterize the in vitro replication kinetics of two EHV-1 N strains in CD172a⁺ cells and investigate if the replication of these strains is similarly silenced as shown for EHV-1 NN strains. We found that EHV-1 N replication was restricted to 7–8% in CD172a⁺ cells compared to 100% in control RK-13 cells. EHV-1 N replication was not delayed in CD172a⁺ cells but virus production was significant lower (10^3.0 TCID₅₀/10⁵ inoculated cells) than in RK-13 cells (10^8.5 TCID₅₀/10⁵ inoculated cells). Approximately 0.04% of CD172a⁺ cells produced and transmitted infectious EHV-1 to neighbour cells compared to 65% of RK-13 cells. Unlike what we observed for the NN strain, pretreatment of CD172a⁺ cells with histone deacetylases inhibitors (HDACi) did not influence the replication of EHV-1 N strains in these cells. Overall, these results show that the EHV-1 replication of N strains in CD172a⁺ cells differs from that observed for NN strains, which may contribute to their different pathogeneses in vivo.