温度、光强和密度对条斑紫菜壳孢子放散的影响

在实验室内可控条件下,用充气培养的条斑紫菜成熟的壳孢子囊枝作材料,研究温度(5～20℃),光强(5～115μmol／m^2.s)和壳孢子囊枝的密度(0．075～1．709mg／ml)对壳孢子放散的影响。结果表明：(1)在5～20℃范围内,壳孢子均可以放散,温度越低,壳孢子开始放散得越早．但高峰期不明显,且放散的周期很长;20℃是最适宜的放散温度,放散的壳孢子数量多,放散集中。(2)壳孢子的放散在低光强和高光强条件下都较差,57μmol／m^2.s条件下壳孢子放散量多而集中。(3)壳孢子囊枝的密度影响壳孢子放散,低密度条件下壳孢子放散快但总量少;密度太高．壳孢子放散极其缓慢;适宜的壳孢子囊枝密度有利于壳孢子放散。     

光合细菌FP04的筛选及对中华鳖养殖水质和生产效益的影响

从入海排污口污泥中筛选到一株有较强净化养殖水质能力的光合细菌,初步鉴定其为红螺菌,命名为FP04。实验室试验表明,FP04能有效降低养殖污水的CODcr含量。在中华鳖的养殖水体中加入不同浓度的FP04,结果与对照组比较,FP04可显著降低养殖水体中的氨氮和化学需氧量,并可减少甲鱼病害发生,提高甲鱼养殖成活率和增重率,其中以养殖水体中FP04浓度为9×104CFU/mL的效果最好,成活率和增重率分别提高14%和31%。     

3种植物生长调节剂对坛紫菜自由丝状体生长与光合色素含量的影响

采用单因素分析法,比较研究了添加3种外源植物生长调节剂(吲哚乙酸IAA、2,4-二氯苯氧乙酸2,4-D、激动素KT)对野生型坛紫菜(Pyropia haitanensis)自由丝状体生长及光合色素含量的影响。结果表明:与对照组相比,低浓度的IAA(0.5~4.0 mg·L~(-1))和KT(0.5~2.0 mg·L~(-1))对藻体的特定生长率有显著影响,以2.0 mg·L~(-1)IAA和1.0 mg·L~(-1)KT对藻体的促生长效应最大,培养25 d时藻体鲜重增加最大,分别是对照组的1.90倍和1.52倍(P0.05)。高浓度的IAA(6.0~10.0 mg·L~(-1))和KT(4.0~10.0 mg·L~(-1))却会抑制藻体生长(P0.05)。培养25 d时,与对照组相比,2.0 mg·L~(-1)IAA和1.0 mg·L~(-1)KT均有利于叶绿素a(Chl a)和类胡萝卜素(Car)的合成,Chl a含量分别增加了23.7%和23.8%;Car含量分别增加了31.0%和28.6%(P0.05)。然而,高浓度的IAA和KT(6.0、10.0 mg·L~(-1))不利于Chl a的合成,其处理浓度越高,Chl a含量下降越多。与对照组相比,较低浓度的IAA(1.0~2.0 mg·L~(-1))明显促进藻红蛋白(PE)和藻蓝蛋白(PC)合成,其中2.0 mg·L~(-1)IAA处理组PE、PC含量最高,分别增加了59.1%和45.7%(P0.05)。较低浓度的KT(0.5~2.0 mg·L~(-1))均有利于PE、PC合成,其中0.5 mg·L~(-1)KT处理组的PE、PC含量增加最多,分别提高了48.4%和50.5%(P0.05)。高浓度的IAA(6.0、10.0 mg·L~(-1))和KT(10.0 mg·L~(-1))则明显降低了PE、PC合成(P0.05)。2,4-D对藻体的特定生长率和光合色素合成无显著影响(P0.05)。     

羊栖菜马尾藻光合作用与水温、光强的关系

羊栖菜马尾藻在不同水温、光强下，光合作用各有其明显的规律性，有适宜的水温和光强范围。光合作用的适宜水温约为１５－２５℃，而以２０℃为最适水温。光饱和产争光合速度随水温２０，１５，２５，１０℃依次降低。根据测定结果，本文对其在羊栖菜马尾藻生产上的合理应用，促使养殖技术和产量的提高，进行了探讨。     

樱桃透光和郁闭树冠相对光照强度及其果实品质和产量的差异

 以13年生‘红灯’甜樱桃（Prunus avium L.）为试材,应用树冠分格方法,研究了树冠透光和郁闭两种冠型内相对光照强度及其果实品质和产量的差异,以及相对光照强度与果实产量品质的关系。结果表明,两种树冠内相对光照强度均自下而上逐渐增高,透光和郁闭树冠小于30%的相对光照区域分别占树冠总体积的25.23%和52.78%。透光树冠果实分布均匀,主要集中在树冠1.5～2.5 m的高度;而郁闭树冠果实分布差异较大,主要在树冠的外围和上部;产量分别是9.02t.hm-2和3.53t.hm-2。果实品质因素与相对光照强度的回归分析表明樱桃单果质量、果实硬度、果实可溶性固形物含量、可滴定酸含量、固酸比最佳的相对光照强度值分别为76.52%、46.84%、100.00%、41.63%和75.77%。     

Production protocol development for greenhouse cut Linaria, Lupinus, and Papaver flowers

Linaria maroccana Hook. f. Ann., ‘Lace Violet’, Lupinus hartwegii ssp. cruikshankii Lindl. ‘Sunrise’ and Papaver nudicaule L. ‘Meadow Pastels’ seeds were directly sown into 105 cell plug trays and received either ambient light or supplemental high intensity discharge (HID) lighting. For each species, a 2 × 3 × 3 factorial was used with two light intensities during propagation, three transplant stages, and three night temperatures. Seedlings were transplanted at the appearance of 2–3, 5–6, or 8–9 true leaves. Transplanted Linaria and Papaver seedlings were placed at 5/11, 10/16, or 15/21 ± 1 °C night/day temperatures and Lupinus seedlings were placed at 15/24, 18/25, or 20/26 ± 2 °C night/day temperatures. For this study, the optimum production temperature for Linaria was 10/16 °C as the cut stems produced at 15/21 °C were unmarketable and production time was excessively long at 5/11 °C. At 10/16 °C, Linaria seedlings should be transplanted at the 2–3 leaf stage to maximize stem number, stem length and profitability. For Lupinus the optimum temperature was 15/24 °C due to long stems and high profitability per plant. Lupinus seedlings should be transplanted at the 2–3 leaf stage when grown at 15/24 °C to obtain the longest and thickest stems; however, $/m² week was higher for plants transplanted at the 8–9 leaf stage due to less time in finishing production space. For Papaver, the 15/21 °C temperature was optimal as that temperature produced the longest stems in the shortest duration, resulting in the highest $/m² week. At 15/21 °C Papaver plants should be transplanted at the 2–3 leaf stage. Supplemental HID lighting had no effect on any of the species.     

Characteristics of phosphorus uptake kinetics of poinsettia and marigold

In a previous experiment it has been found that maximum uptake rate (I_max), Michaelis constant (K_m), and minimum nutrient concentration (C_min) as plant physiological characteristics may be important for phosphorus (P) uptake in peat-substrate. Thus, variation of P uptake parameters was evaluated with a series of depletion studies for poinsettia (Euphorbia pulcherrima) and marigold (Tagetes patula) under fluctuating climatic conditions and different developmental stages.     

Does root-sourced ABA play a role for regulation of stomata under drought in quinoa (Chenopodium quinoa Willd.)

The Andean seed crop quinoa (Chenopodium quinoa Willd.) is traditionally grown under drought and other adverse conditions that constrain crop production in the Andes, and it is regarded as having considerable tolerance to soil drying. The objective of this research was to study how chemical and hydraulic signalling from the root system controlled gas exchange in a drying soil in quinoa. It was observed that during soil drying, relative g_s and photosynthesis A_max (drought stressed/fully watered plants) equalled 1, until the fraction of transpirable soil water (FTSW) decreased to 0.82 ± 0.152 and 0.33 ± 0.061, respectively, at bud formation, indicating that photosynthesis was maintained after stomata closure. The relationship between relative g_s and relative A_max at bud formation was represented by a logarithmic function (r² = 0.79), which resulted in a photosynthetic water use efficiency WUE_Amax_/gs$\text{WU}{\text{E}}_{A_{\text{max}}/g_{\text{s}}}$ of 1 when FTSW > 0.8, and increased by 50% with soil drying to FTSW 0.7–0.4. Mild soil drying slightly increased ABA in the xylem. It is concluded that during soil drying, quinoa plants have a sensitive stomatal closure, by which the plants are able to maintain leaf water potential (ψ_l) and A_max, resulting in an increase of WUE. Root originated ABA plays a role in stomata performance during soil drying. ABA regulation seems to be one of the mechanisms utilised by quinoa when facing drought inducing decrease of turgor of stomata guard cells.     

温度、盐度和光照强度对鼠尾藻氮、磷吸收的影响

在实验室条件下,研究了不同的温度和盐度组合,温度和光照强度组合对鼠尾藻(Sargassum thunbergii)氮、磷吸收速率的影响.结果表明,上述3个环境因子对鼠尾藻氮、磷吸收速率均有显著影响.其中,温度和盐度对鼠尾藻氮、磷吸收速率有极显著影响(P<0.01),二者交互作用也极显著(P<0.01).在盐度20、温度25℃条件下和盐度30、温度30℃条件下,鼠尾藻对氮有较高吸收速率,分别为11.26μmol/[g(dw)·h]和11.01 μmol/[g(dw)·h];在盐度40、温度15～30℃范围内对磷的吸收速率较大,达到1.5μmol/[g(dw)·h]以上.温度和光照对鼠尾藻氮、磷吸收速率均有极显著影响(P<0.01),二者交互作用极显著(P<0.01).在温度15℃和光照强度140～180μE/(m2·s)以及温度20～25℃和光照强度60～100 μE/(m2·s)条件下,鼠尾藻对氮有较高吸收速率,均在9.60 μmol/[g(dw)·h]以上;在温度25℃和光照强度60μE(m2·s)条件下,鼠尾藻对磷的吸收速率达到最大,为1.30 μmol/[g(dw)·h].本研究结果表明,鼠尾藻总体上对水体中的氮、磷均具有较高的吸收速率,且能较好地同时吸收NH4+-N和NO3--N,显示了它对海水环境中营养盐具有较强的吸收能力.