滤食性贝类对浮游植物群落增殖作用的研究

报道了在室内实验条件下贝类对浮游植物促长（间接）作用的研究结果,数据表明,贝类对浮游植物有明显的促长作用,并且浮游植物的增长与贝类密度呈正相关,贝类对浮游植物的促长作用随藻类种类的不同具有较大的差别,主要取决于藻类对营养盐的需求量,由于贝类排泄产物和排泄量存在种间差异,因而对浮游植物具有不同的促长效果。     

林地覆盖对雷竹林土壤微生物特征及其与土壤养分制约性关系的影响

为了探讨林地覆盖雷竹林退化机理,给退化雷竹林恢复提供理论参考,对不同覆盖年限(CK、1、3 a 和6 a) 雷竹林土壤微生物区系组成和生物量碳(C_mic)、氮(N_mic)、磷(P_mic)等特征因子进行了测定,并分析了其与土壤养分的制约性关系。结果表明:(1) 雷竹林土壤微生物以细菌为主,真菌次之,放线菌最少,分别占土壤微生物总量的90.11%-98.03%、1.04%-9.22%和0.67%-1.37%。随覆盖年限增加,细菌、放线菌比率呈下降趋势,真菌比率呈上升趋势;土壤微生物总数、细菌和放线菌数量及C_mic、N_mic、P_mic均呈先升高后降低的变化趋势,试验雷竹林间差异极显著,真菌数量总体呈极显著升高趋势。(2)雷竹林土壤微生物特征因子与土壤有机质(SOM)、全氮(TN)、全磷(TP)、碱解氮(Available nitrogen, AN)和pH均呈显著或极显著相关,其中,CK和覆盖1 a、3 a雷竹林土壤微生物特征因子与土壤养分主要呈正相关,与pH呈负相关,而覆盖6 a雷竹林则相反。(3)不同覆盖年限雷竹林土壤养分与土壤微生物的制约性关系存在一定的差异,CK雷竹林土壤SOM、TN、AN、速效钾(AK)和pH主要影响土壤C_mic、N_mic和细菌,覆盖1 a雷竹林土壤SOM、TN、TP和AK主要影响土壤P_mic、放线菌和细菌,覆盖3 a雷竹林土壤SOM、TN、速效磷(AP)和AN主要影响土壤N_mic、放线菌和真菌,覆盖6 a雷竹林土壤SOM、TN和pH主要影响土壤N_mic、真菌。研究表明:长期覆盖雷竹林土壤细菌、放线菌数量与比例明显降低,真菌数量与比例明显提高,土壤养分与土壤微生物的制约性作用关系会发生较为明显变化,产生土壤障害,这是覆盖雷竹林退化的主要原因之一。     

Suction volume and filtering efficiency of silver carp (Hypophthalmichthys molitrix Val.) and bighead carp (Aristichthys nobilis Rich.)

Experiments were conducted to measure the suction volume of silver carp and bighead carp of age 1 + with respiratory chamber, and to calculate the suction volume and the filtering efficiency with respect to changes in concentrations of food particles. Suction volume (B. ml/mouth) and filtering efficiency (E. %) were calculated using the following formula: C ₁=C₀(1-BE/v)ⁿ where C₀ and C₁ were the concentrations of specific food particles at the beginning and at the end of experiment, respectively, V was the volume (ml) of experimental water, and n was the total number of observation of suction made during the experimental period. The relationships between suction volume (ml/mouth) of age I+ silver carp (B_h) and bighead carp (B_a) and their standard lengths (L, cm) were: B _h=0.561L-8.94, B_a= 0.627L-7.48 while those of the fingerlings were: B _h= O.l70L-0.837, B_a= 0.157L-0.418. The suction volume of the fingerlings was mainly affected by fish size, the function of temperature between 15 and 25° C being negligible. However, temperature affected filtering rate (filtered volume per unit time) through its effect on filtering frequency. The filtering efficiency of the fishes for rotifers (Brachionus caliciflorus) was 100 per cent. The relationships between filtering efficiency and sizes of food particles smaller than or equal to that of a rotifer were: E _h=25.1 ln e.s.d. -13.6, E_a=22.2 In e.s.d. -33.1 where E_h and E_a were filtering efficiency of silver carp and bighead carp, respectively, and e.s.d. was the equivalent spherical diameter (μm) of food particles.     

盐碱池塘围隔生态系统的悬浮物结构及有机碳库储量

1 998年 4～ 7月对高青盐碱池塘单养鲢和罗非鱼围隔生态系统颗粒悬浮物构成和各有机碳库储量及动态进行了研究。结果表明 ,浮游生物的干重 (PZ)占总颗粒悬浮物干物质 (TS)的 4.2 6%～ 2 5 .97% ,平均 1 2 %。各围隔浮游植物干重(DWP)平均值变化范围为 0 .1 6～ 0 .70 mg/L,有鱼围隔均比无鱼围隔的大。浮游动物干重 (DWZ)平均值变化范围为0 .3 2～ 2 .81 mg/L,养鲢围隔中最小 ,小于无鱼对照围隔 ,养罗非鱼围隔明显高于养鲢围隔。颗粒悬浮物的灰分含量平均值为 42 .3 8%。溶解有机碳 (DOC)、颗粒有机碳 (POC)库储量平均值分别为 5 .40± 1 .61 mg C/L和 1 .96± 0 .96mg/L。各处理围隔间颗粒有机物的 C/N比的平均值比较接近 ,总平均值为 6.97± 0 .2 4。 TOC、DOC和 POC比例为 1∶ 0 .73∶0 .2 7。浮游生物碳和腐质颗粒碳占 POC的比例的平均值分别为 3 4.65 %和 65 .3 5 %。腐质颗粒碳、浮游动物碳与浮游植物碳的比例为 9.2 9∶ 3 .71∶ 1。浮游生物碳中浮游动物碳占 78.8% ,浮游植物碳占 2 1 .2 %。浮游动物碳比浮游植物碳高 ,这可能是内陆盐水的通性。盐碱池塘围隔生态系统颗粒有机碳 (POC,mg C/L)与浮游植物叶绿素 a(Chla,μg/L)和悬浮颗粒有机物 (SO,mg/L)之间存在显著的正相关关系 ,其回归方程分别为     

中国对虾继饥饿后的补偿生长研

1999年7至8月份,在25.0±0.5℃条件下对中国对虾（湿重,1.454±0.150g）进行了不同时间的饥饿处理后再供食的恢复生长实验。对照组C连续饱食投喂32d;处理组S4、S8和S12分别饥饿4、8和12d后再饱食投喂28、24和20d。主要结果如下饥饿结束时各处理组的干重和湿重显著低于对照组（P<0.05）;实验结束时S4组和对照组间的干重和湿重差异不显著（P>0.05）,而S8和S12两组的干重和湿重仍显著低于对照组（P<0.05）;恢复生长后各处理组的湿重摄食率显著高于对照组（P<0.05）。实验结果表明,中国对虾继饥饿后再恢复喂食出现完全或部分补偿生长效应,且这种补偿生长效应主要是通过恢复生长阶段食欲增大,摄食水平提高实现的。     

盐碱池塘细巧华哲水蚤对浮游植物的摄食生态研究

利用常规显微镜直接计数法和叶绿素 a法研究了盐碱池塘细巧华哲水蚤 ( Sinocalanustenellus)对浮游藻类的原位摄食率及其影响因素。测得该水蚤对水柱浮游植物的滤水率为 1 .73～ 1 5 5 .1 6μl/ ( ind.· h) ,摄食率为 92～ 2 5 38cell/( ind.· h)或 0 .7～ 2 7.7ng C/ ( ind.· h)。两种方法测定的滤水率和摄食率基本相符 ( p>0 .5 ,t检验 )。该水蚤可有选择地滤食诸如小色球藻、光甲藻、绿裸藻 ,单生卵囊藻和小环藻等 ,其选择性指数分别为 0 .81、0 .75、0 .72、0 .6 1和 0 .35。不同光处理下细巧华哲水蚤的滤食率多数情况是无光时摄食率高。在本实验的条件下该水蚤在饥饿后的滤水率和摄食率与正常情况相比均显著降低 ( P<0 .0 1 ,t检验 )。     

SNHG16 as the miRNA let-7b-5p sponge facilitates the G2/M and epithelial-mesenchymal transition by regulating CDC25B and HMGA2 expression in hepatocellular carcinoma

Long noncoding RNAs (lncRNAs) play crucial roles in hepatocellular carcinoma (HCC). However, the underlying molecular mechanisms of small nucleolar RNA host gene 16 (SNHG16) for regulating the cell cycle and epithelial to mesenchymal transition (EMT) remain elusive. In this study, SNHG16 expression profiles of HCC tissues or cell lines were compared with those of normal tissues or hepatocyte cell line. The effect of SNHG16 knockdown in HCC cell lines was investigated by using in vitro loss-of-function experiments and in vivo nude mouse experiments. The potential molecular regulatory mechanism of SNHG16 in HCC progression was investigated by using mechanistic experiments and rescue assays. The results revealed that SNHG16 was highly expressed in HCC tissues and cell lines, which predicted poor prognosis of HCC patients. On one hand, the downregulation of SNHG16 induced G2/M cell cycle arrest, inducing cell apoptosis and suppression of cell proliferation. On the other hand, it inhibited cell metastasis and EMT progression demonstrated by in vitro loss-of-function cell experiments. Besides, knockdown of SNHG16 increased the sensitivity of HCC cells to cisplatin. For the detailed mechanism, SNHG16 was demonstrated to act as a let-7b-5p sponge in HCC. SNHG16 facilitated the G2/M cell cycle transition by directly acting on the let-7b-5p/CDC25B/CDK1 axis, and promoted cell metastasis and EMT progression by regulating the let-7b-5p/HMGA2 axis in HCC. In addition, the mechanism of SNHG16 for regulating HCC cell proliferation and metastasis was further confirmed in vivo by mouse experiments. Furthermore, these results can provide new insights into HCC treatment and its molecular pathogenesis, which may enlighten the further research of the molecular pathogenesis of HCC.     

CK2 phosphorylates TNFAIP1 to affect its subcellular localization and interaction with PCNA

TNFAIP1 is a protein which can be induced by tumor necrosis factorα (TNFα) and interleukin-6 (IL-6), it may play roles in DNA synthesis, DNA repair, cell apoptosis and human diseases. However, very little has been known about how TNFAIP1 acts in these physiological processes. In this paper, CK2β was identified as a partner of TNFAIP1 by screening the HeLa cDNA library in yeast two-hybrid system with TNFAIP1 as a bait. Furthermore, it was demonstrated that CK2 could phosphorylate TNFAIP1 in vitro and in vivo, which facilitated the distribution of TNFAIP1 in nucleus and enhanced its interaction with PCNA. It is suggested that the phosphorylation of TNFAIP1 may be required for its functions.