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The results showed that LC50 were 0.0095 and 0.0082 mg/L at 24 h and 48 h with safe concentration of 0.0018 mg/L for Zoea Ⅰ. For Zoea Ⅱ, LC50 were 0.019 and 0.010 mg/L at 24 h and 48 h with safe concentration of 0.0038 mg/L.

三疣梭子蟹Ⅰ期溞状幼体24 h LC50和48h LC50分别为0.0095 mg/L和0.0082 mg/L，安全质量浓度为0.0018 mg/L；三疣梭子蟹Ⅱ期溞状幼体24 h LC50和48h LC50。

The safety concentration of ammonia nitrogen on the zoea larvae, mysis larvae and postlarvae was 0.295mg/L, 0.724mg/L, 1.072 mg/L respectively, and that of sulfurated hydrogen was 0.0430mg/L, 0.0553mg/L, 0.0705mg/L.

氨氮和硫化氢对日本对虾蚤状幼体、糠虾幼体和仔虾的安全浓度分别为：0.295，0.0430；0.724，0.0553；1.072，0.0705mg/L。

Plantlet regeneration from cotyledon of Citrullus lanatus cv. Zhangkang No. 4 was studied. The results showed that aseptic seedlings should be cultured in dark for 3d, then exposed to a photoperiod of 16/8h/d for 3d. The callus induction rate was higher in cotyledons placed facing downwards to the medium than in those facing upwards. The highest induction rate occurred in MS medium containing 6-BA (2.0mg/L), kinetin (1.0mg/L)and GA3 (1.0mg/L). The induction initiated in dark and took 7 days, while callus growth and differentiation proceeding for 7 days under 16/8h light-dark cycles. A highest rate of embryogenic callus was obtained after 3 successive subcultures.

以无子西瓜郑抗4号无菌苗子叶为外植体，进行了体细胞胚发生及植株再生的研究，结果表明，无菌苗应先进行3d暗培养，然后采取光照16h/d和黑暗8h/d培养3d；将子叶的叶面朝下放置于培养基上的愈伤组织诱导率高于叶面朝上的培养方式；子叶诱导胚性愈伤组织的最适培养基配方为MS+6-BA2.0mg/L+KT1.0mg/L+GA31.0mg/L；诱导需要在黑暗条件下启动，进行7d暗培养，而生长分化于光照16h/d和黑暗8h/d条件下培养7d；继代3次得到的胚性愈伤组织最多；最适生根培养基配方为1/2MS+IBA0.3mg/L。

The low phosphate scale and corrosion inhibitor consists of hydroxyl ethylidene bisphosphoric acid in 0.5-1 mg/l, hydrolyzed polymaleic anhydride in 0.5-2 mg/l and polyasparic acid in 1-2 mg/l, with the total concentration being 3 mg/l.

还含有0.5～2mg/L的水解聚马来酸酐和1～2mg/L的聚天冬氨酸，低磷阻垢缓蚀剂的总质量分数之和为3mg/L。

Cells in the induction group were incubated in 1.5 mL of osteoinductive medium, supplemented with 10-8 mol/L dexamethasone, 10 mol/L β-glycerophosphoric acid, and 50 mg/L vitamin C.

选取第3代骨髓间充质干细胞和脂肪间充质干细胞，按5×107 L-1接种后各分为2组：诱导组加入含10-8 mol/L地塞米松、10 mol/L β-甘油磷酸、50 mg/L维生素C的成骨诱导培养基1.5 mL，未诱导组不加入成骨诱导培养基。

METHODS: The third passage of BMSCs and AMSCs at a density of 5×10^7 L^(-1) were divided into two groups. Cells in the induction group were incubated in 1.5 mL of osteoinductive medium, supplemented with 10^8 mol/L dexamethasone, 10 mol/L β-glycerophosphoric acid, and 50 mg/L vitamin C. Cells in the non-induction group were not treated with osteoinductive medium.

选取第3代骨髓间充质干细胞和脂肪间充质干细胞，按5×10^7L^(-1)接种后各分为2组：诱导组加入含10^8mol/L地塞米松、10mol/L β-甘油磷酸、50mg/L维生素C的成骨诱导培养基1.5mL，未诱导组不加入成骨诱导培养基。

When 2.0 g/L of malate was added to the fermentation medium, the metabolic flux of byproducts L-Ala and lactic acid decreased by 22.1% and 16.5%. At the same time, the metabolic channeled to EMP and glyoxyl circle decreased by 2.26% and 9.09%. However, the metabolic flux channeled to HMP increased by 2.26%.The metabolic flux channeled to the L-glutamic acid synthesis pathway increased from 73.59% to 79.92%.

在L-谷氨酸发酵中、后期添加2.0 g/L苹果酸后，合成副产物L-丙氨酸和乳酸的代谢流量明显减少，分别降低了22.1%和16.5%，EMP途径和乙醛酸循环的代谢流分别减少了2.26%和9.09%，HMP途径的代谢流增加了2.26%，而L-谷氨酸生物合成的代谢流从73.59%增长至79.92%，较未添加前提高了6.33%。

The results show that by providing wastewaters pH of about 3 and reaction time of 2 hours, the quantity of H2O2 of 40 mL/L, the concentration of ferrous iron is 0.4 g/L, the effluent of microelectrolysis goes into Biological contact oxidation process, in which DO, HRT and volume load are 4.5 mg/L, 10 hours and 1.0 kg CODCr/(m3·d) respectively, satisfying the first grade of the national standard.

结果表明，在废水pH值为3左右、反应时间2 h的前提下，双氧水投加量40 mL/L，二价铁离子质量浓度为0.4 g/L，再经过微电解处理后的出水进入接触氧化阶段。在溶解氧为4.5 mg/L左右，水力停留时间为10 h、容积负荷1.0 kg CODCr/（m3·d）左右的条件下，出水CODCr小于100 mg/L，可达到国家对丙烯腈废水处理要求的一级标准。

"Over the l ast two years, a new sty l ing phi l osophy that we ca l l L-finesse, has taken shape at Lexus Design," said Wahei Hirai

丰田汽车公司负责全球设计的官员Wahei Hirai表示：&在过去两年里，LEXUS雷克萨斯形成了一种全新的设计理念，我们称之为L-finesse。&

Result The optimum medium formula for protocorm propagation in tissue culture of C. grandiflorium was MS+0.1 mg/L 6-BA. The suitable medium for protocorm induction and differentiation in tissue culture of C. grandiflorum was WS+1.5 mg/L 6-BA+0.3 mg/L NAA with the bud-inducing rate up to 130%. The suitable medium for root inducement was 1/2MS+0.2 mg/L NAA+1.0 mg/6-BA and the survival rate of in vitro plantlets after transplanting was 78%.

结果］大花蕙兰组织培养原球茎粉殖以MS+0.1 mg/L NAA+2.0 mg/L6-BA培养基配方最好；适合大花蕙兰组织培养原球茎诱导分化的培养基配方为MS+1.5 mg/L6-BA+0.3 mg/L NAA，诱导出芽率可达130%；适合大花蕙兰诱导生根的培养基配方为1/2 MS+0.2 mg/L NAA+1.0 mg/L6-BA，试管苗移栽后成活率为78%。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。