Characteristics and mechanisms of the hydroponic bio-filter method for purification of eutrophic surface water

The hydroponic bio-filter method (HBFM) was adopted to purify eutrophic surface water. The average removal efficiency of total nitrogen (TN) and total phosphorus (TP) was 16.8% and 30.8%, respectively, at the hydraulic loading rate (HLR) of 3.0 m³ (m² d)⁻¹. The mass removal rate of TN and TP accordingly reached 1.0 and 0.1 g (m² d)⁻¹ separately. The sedimentation of particulate nitrogen and phosphorus played a major role in removal of nitrogen and phosphorus, which contribute 62.2% and 75.9%, respectively. The optimal HLR of HBFM ranged from 3.0 to 4.0 m³ (m² d)⁻¹. The sediment in midstream reached a maximum nitrification potential of 4.76 × 10⁻⁶ g (g h)⁻¹, while upstream it reached a maximum denitrification potential of 8.1 × 10⁻⁷ g (g h)⁻¹. The distribution of nitrification potential corresponded to the ammonium-oxidizing bacteria density. The key for improving nitrogen removal efficacy of HBFM system consisted of changing the nitrification/denitrification region distribution and accordingly enhancing the denitrification process. The sum of dissolved nitrogen removed by denitrification and plant assimilation was nearly equal to the amount released by sediment. Secateur length of Nasturtium officinale had some effect on its uptake rate. The length of cut should be less than 10 cm at a time. The harvesting frequency of once a month for N. officinale had no influence on nitrogen and phosphorus removal.     

Nursery Nitrogen Loading Improves Field Performance of Bareroot Oak Seedlings Planted on Abandoned Mine Lands

Although mine reclamation sites are important targets for ecological restoration, they are generally difficult to regenerate successfully. We evaluated the importance of nursery nutrient loading as a new approach to enhance forest restoration on abandoned mine lands. Northern red oak ( Quercus rubra ) and White oak ( Q. alba ) seedlings were nitrogen (N) loaded for 18 weeks at a bareroot nursery in southern Indiana, United States. Fertility treatments followed conventional or modified exponential functions to synchronize N supply with plant demand. Subsequently, nursery-grown seedlings were outplanted the following year onto a mine reclamation site in southwestern Indiana to evaluate effects of nursery N loading on first-year field performance. Nursery N loading promoted total plant dry mass production 25–129% in Red oak and 50–184% in White oak compared to unfertilized plants. Nitrogen loading increased N content 88–145% and potassium (K) content 16–71% for Red oak and N content 124–250% and K content 16–93% for White oak relative to controls. When outplanted, N loading resulted in high seedling survival (>84%) and increased total plant dry mass production 14–30% for Red oak and 23–52% for White oak. Nitrogen loading increased plant N uptake 14–102% in Red oak and 32–105% in White oak under field conditions. Exponential N loading demonstrates potential as a viable technique to improve seedling outplanting performance and reclamation success in Indiana and elsewhere.     

Current status and conservation of Pistacia germplasm

The genetic erosion of Pistacia germplasm has been highlighted in many reports. In order to emphasize this and to focus more attention on this subject, national and international (especially IPGRI and IFAR) institutions have initiated projects proposing to characterize, collect and conserve Pistacia germplasm. Therefore, this paper reviews recent research concerning conventional (in situ and ex situ) and unconventional biotechnological conservation strategies applied to the preservation of Pistacia germplasm. As regards conventional conservation, the majority of germplasm collections of Pistacia species are preserved on farms (in situ) and in seed and field genebanks (ex situ), as well as in the wild, where they are vulnerable to unexpected weather conditions and/or diseases. Hence, complementary successful unconventional in vitro methods (organogenesis, somatic embryogenesis and micrografting) and slow-growth storage conditions for medium-term preservation of Pistacia are presented together with the morphological and molecular studies carried out for the characterization of its species in this review. Moreover, special attention is additionally focused on cryopreservation (dehydration- and vitrification-based one-step freezing techniques) for the long-term preservation of Pistacia species. Possible basic principles concerning the establishment of a cryobank for the successful conservation of Pistacia germplasm are also discussed.     

Closure of plasmodesmata in maize (Zea mays) at low temperature: a new mechanism for inhibition of photosynthesis

Background and Aims

Photosynthesis is one of the processes most susceptible to low-temperature inhibition in maize, a tropical C4 crop not yet fully adapted to a temperate climate. C4 photosynthesis relies on symplasmic exchange of large amounts of photosynthetic intermediates between Kranz mesophyll (KMS) and bundle sheath (BS) cells. The aim of this study was to test the hypothesis that the slowing of maize photosynthesis at low temperature is related to ultrastructural changes in the plasmodesmata between KM and BS as well as BS and vascular parenchyma (VP) cells.

Methods

Chilling-tolerant (CT) KW 1074 and chilling-sensitive (CS) CM 109 maize (Zea mays) lines were studied. The effect of moderate chilling (14 °C) on the rate of photosynthesis, photosynthate transport kinetics, and the ultrastructure of plasmodesmata linking the KMS, BS and VP cells were analysed. Additionally, the accumulation of callose and calreticulin was studied by the immunogold method.

Key Results

Chilling inhibited photosynthesis, photosynthate transfer to the phloem and photosynthate export from leaves in both lines. This inhibition was reversible upon cessation of chilling in the CT line but irreversible in the CS line. Simultaneously to physiological changes, chilling induced swelling of the sphincters of plasmodesmata linking KMS and BS cells and a decreased lumen of the cytoplasmic sleeve of plasmodesmata at the BS/VP interface in the CS line but not in the CT line. Accumulation of calreticulin, which occurred near the neck region of the closed plasmodesmata was observed after just 4 h of chilling and over-accumulation of callose at the KMS/BS and BS/VP interfaces occurred after 28 h of chilling.

Conclusions

Stronger chilling sensitivity of the CM 109 maize line compared with the KW 1074 line, shown by decreased photosynthesis and assimilate export from a leaf, is related to changes in the ultrastructure of leaf plasmodesmata at low temperature. The chain of reactions to chilling is likely to include calreticulin action resulting in rapid and efficient closure of the plasmodesmata at both KMS/BS and BS/VP interfaces. Callose deposition in a leaf was a secondary effect of chilling.     

黄河口不同氮基质碱蓬种子萌发及幼苗生长对盐分及氮输入的响应

2014年4-11月,选择黄河入海口北部滨岸高潮滩的碱蓬湿地为研究对象,基于野外原位氮负荷增强模拟试验(N0,无额外氮输入;N1,低氮输入;N2,中氮输入;N3,高氮输入),获取相应的不同氮基质种子(S0,S1,S2和S3),以研究其发芽率以及幼苗生长状况对不同盐分胁迫和氮浓度交互作用的响应。结果表明,不同氮负荷影响下碱蓬成熟种子中的氮含量整体表现为S2S0S1S3,中氮输入更利于种子中氮养分的累积。盐分和氮交互作用下4种氮基质种子的发芽率总体表现为S2S1S0S3(P0.05),S2在不同盐分胁迫下的发芽率最高,幼苗的生长状况也最好。随着盐分的增加,4种氮基质种子的发芽率及幼苗生长状况均受到一定程度的抑制,但较低的盐分有助于其幼苗长度的增长,且随着氮输入量的增加这种抑制作用可得到一定程度缓解。盐分胁迫、氮浓度和种子类型作为单独因素出现时对碱蓬的发芽率、幼苗长度、鲜重和干重均产生显著影响,除幼苗长度受氮浓度和盐分胁迫交互作用的影响达到显著水平外(P0.05),其他因子交互作用对诸生态指标的影响并不明显。研究发现,不同氮输入处理不仅改变了原生环境碱蓬种子的氮含量,而且也使这些具备不同氮基质的种子对不同盐分胁迫与氮浓度环境具有不同的生态适应对策,中氮输入下的碱蓬种子(S2)无论在萌发率还是在幼苗生长状况上均优于其他氮基质的种子。未来,随着黄河口新生湿地氮养分供给的不断增加,当湿地氮养分达到中氮水平时,将更有利于碱蓬种子的萌发以及幼苗的生长,当氮养分达到更高水平时,碱蓬种子的萌发以及幼苗生长可能会受到一定程度的抑制。     

沙柳原料高浓度底物酶解发酵乙醇工艺

为了提高沙柳生物转化过程的经济可行性,考察了沙柳原料经过蒸爆、超微粉碎+稀酸、超微粉碎+稀碱预处理后高浓度底物补料酶解的效果,并对其高浓度水解糖液进行了乙醇发酵。结果表明:蒸爆处理法水解效果最好,通过补料酶解,底物质量分数可以达到30%,酶解液中总糖质量浓度达到132 g/L,葡萄糖质量浓度105 g/L;超微粉碎+稀酸预处理原料底物质量分数可以达到22%,酶解液中总糖质量浓度达到123 g/L,葡萄糖质量浓度73 g/L;超微粉碎+稀碱预处理原料底物质量分数可以达到22%,酶解液中总糖质量浓度133 g/L,葡萄糖质量浓度77 g/L。3种预处理使沙柳原料的酶解糖液都可以较好地被酿酒酵母利用发酵产乙醇,蒸爆处理原料的酶解糖液乙醇发酵效果最好,乙醇质量浓度达到47 g/L。     

COM1, a factor of alternative non‐homologous end joining,lagging behind the classic non‐homologous end joining pathway in rice somatic cells

The role of rice (Oryza sativa) COM1 in meiotic homologous recombination (HR) is well understood, but its part in somatic double‐stranded break (DSB) repair remains unclear. Here, we show that for rice plants COM1 conferred tolerance against DNA damage caused by the chemicals bleomycin and mitomycin C, while the COM1 mutation did not compromise HR efficiencies and HR factor (RAD51 and RAD51 paralogues) localization to irradiation‐induced DSBs. Similar retarded growth at the post‐germination stage was observed in the com1‐2 mre11 double mutant and the mre11 single mutant, while combined mutations in COM1 with the HR pathway gene (RAD51C) or classic non‐homologous end joining (NHEJ) pathway genes (KU70, KU80, and LIG4) caused more phenotypic defects. In response to γ‐irradiation, COM1 was loaded normally onto DSBs in the ku70 mutant, but could not be properly loaded in the MRE11^RNAi plant and in the wortmannin‐treated wild‐type plant. Under non‐irradiated conditions, more DSB sites were occupied by factors (MRE11, COM1, and LIG4) than RAD51 paralogues (RAD51B, RAD51C, and XRCC3) in the nucleus of wild‐type; protein loading of COM1 and XRCC3 was increased in the ku70 mutant. Therefore, quite differently to its role for HR in meiocytes, rice COM1 specifically acts in an alternative NHEJ pathway in somatic cells, based on the Mre11–Rad50–Nbs1 (MRN) complex and facilitated by PI3K‐like kinases. NHEJ factors, not HR factors, preferentially load onto endogenous DSBs, with KU70 restricting DSB localization of COM1 and XRCC3 in plant somatic cells.     

活体肺癌组织玻璃化保存的研究

保存活体的肺癌组织将为肺癌发病基因筛查和靶向药物筛选等体外实验研究提供更完整的样本信息. 本文对活体肺癌组织的玻璃化保存方法进行研究，首先采用针浸法玻璃化保存单块肺癌组织，对所需低温保护剂的浓度和平衡时间进行了优化；其次采用冻存管对多块肺癌组织样本进行玻璃化保存，对低温保护剂溶液体积以及平衡时间进行了优化；最后对慢速冷冻、不加低温保护剂快速冷冻、玻璃化冷冻3种冷冻方法的冻存效果进行比较并通过低温显微分析其冰晶损伤机理.结果表明，20% EG+20% DMSO+0.5 mol/L海藻糖作为低温保护剂，在平衡溶液和玻璃化溶液分别加载3 min和1 min时，针浸法和0.25 ml冻存管内玻璃化冻存，复苏后组织活力最高，分别约为79.96%与80.44%. 免疫组化显示玻璃化保存肺癌组织经过复苏后，相比慢速冷冻和无保护剂快速冷冻，组织结构损伤较小，组织内细胞TUNEL阳性表达较少. 低温显微结果表明，玻璃化保存组织内部及周围只出现少量细小冰晶，而慢速冷冻、快速冷冻组织皆出现明显冰晶.