Integrated transcriptome and proteome analysis provides insight into chilling-induced dormancy breaking in Chimonanthus praecox

Chilling has a critical role in the growth and development of perennial plants.The chilling requirement(CR)for dormancy breaking largely depends on the species.However,global warming is expected to negatively affect chilling accumulation and dormancy release in a wide range of perennial plants.Here,we used Chimonanthus praecox as a model to investigate the CR for dormancy breaking under natural and artificial conditions.We determined the minimum CR(570 chill units,CU)needed for chilling-induced dormancy breaking and analyzed the transcriptomes and proteomes of flowering and non-flowering flower buds(FBs,anther and ovary differentiation completed)with different CRs.The concentrations of ABA and GA3 in the FBs were also determined using HPLC.The results indicate that chilling induced an upregulation of ABA levels and significant downregulation of SHORT VEGETATIVE PHASE(SVP)and FLOWERING LOCUS T(FT)homologs at the transcript level in FBs when the accumulated CR reached 570 CU(IB570)compared to FBs in November(FB.Nov,CK)and nF16(non-flowering FBs after treatment at 16℃for−300 CU),which suggested that dormancy breaking of FBs could be regulated by the ABA-mediated SVP-FT module.Overexpression in Arabidopsis was used to confirm the function of candidate genes,and early flowering was induced in 35S::CpFT1 transgenic lines.Our data provide insight into the minimum CR(570 CU)needed for chilling-induced dormancy breaking and its underlying regulatory mechanism in C.praecox,which provides a new tool for the artificial regulation of flowering time and a rich gene resource for controlling chilling-induced blooming.

Bayesian estimator of human error probability based on human performance data

A Bayesian method for estimating human error probability（HEP） is presented.The main idea of the method is incorporating human performance data into the HEP estimation process.By integrating human performance data and prior information about human performance together,a more accurate and specific HEP estimation can be achieved.For the time-unrelated task without rigorous time restriction,the HEP estimated by the common-used human reliability analysis（HRA） methods or expert judgments is collected as the source of prior information.And for the time-related task with rigorous time restriction,the human error is expressed as non-response making.Therefore,HEP is the time curve of non-response probability（NRP）.The prior information is collected from system safety and reliability specifications or by expert judgments.The（joint） posterior distribution of HEP or NRP-related parameter（s） is constructed after prior information has been collected.Based on the posterior distribution,the point or interval estimation of HEP/NRP is obtained.Two illustrative examples are introduced to demonstrate the practicality of the aforementioned approach.

Study on Toxicity of 9 Biocontrol Microbial Products to Adult Population of Tobacco Beetle,Lasioderrma serricorne(Fabricius)

[Objectives]The paper was to study the toxicity of 9 biocontrol microbial products to adult population of Lasioderrma serricorne.[Methods]Nine biocontrol microbes were used as test materials to study their toxicity to the experimental population of L.serricorne adults.[Results]The toxicities of these biocontrol microbes from low to high at 5 d post spraying were:Luhai Beauveria bassiana powder(LC_(50)=462.752×10^(8) spores/L),Meichongzhi B.bassiana powder(LC_(50)=9713.157×10^(8) spores/L),Yiqiang Bio B.bassiana powder(LC_(50)=11203.321×10^(8)spores/L),Nongbao Bio B.bassiana powder(LC_(50)=12188.866×10^(8) spores/L),Yeshengwang B.bassiana powder(LC_(50)=21685.532×10^(8) spores/L);Fatu Bacillus thuringiensis suspension(LC_(50)=1.0844×10^(8) IU/L),Laojite B.thuringiensis suspension(LC_(50)=2.056×10^(8) IU/L),Lujinwa B.thuringiensis powder(LC_(50)=2.273×10^(8) IU/L),Nongbao Bio B.thuringiensis powder(LC_(50)=18.399×10^(8) spores/L).The toxicities of these biocontrol microbes from low to high at 10 d post spraying were:Nongbao Bio B.bassiana powder(LC_(50)=0.072×10^(8) spores/L),Yiqiang Bio B.bassiana powder(LC_(50)=2.484×10^(8) spores/L),Luhai B.bassiana powder(LC_(50)=44.551×10^(8) spores/L),Meichongzhi B.bassiana powder(LC_(50)=96.447×10^(8) spores/L),Yeshengwang B.bassiana powder(LC_(50)=723.347×10^(8) spores/L);Lujinwa B.thuringiensis powder(LC_(50)=0.0001×10^(8) IU/L),Fatu B.thuringiensis suspension(LC_(50)=0.045×10^(8) IU/L),Laojite B.thuringiensis suspension(LC_(50)=0.0644×10^(8) IU/L),Nongbao Bio B.thuringiensis powder(LC_(50)=1.899×10^(8) spores/L).The toxicities of these biocontrol microbes from low to high at 15 d post spraying were:Meichongzhi B.bassiana powder(LC_(50)=0.001×10^(8) spores/L),Nongbao Bio B.bassiana powder(LC_(50)=0.01×10^(8) spores/L),Yiqiang Bio B.bassiana powder(LC_(50)=0.084×10^(8) spores/L),Luhai B.bassiana powder(LC_(50)=2.370×10^(8) spores/L),Yeshengwang B.bassiana powder(LC_(50)=8.915×10^(8)spores/L);Lujinwa B.thuringiensis powder(LC_(50)=0.16×10^(4) IU/L),Laojite B.thuringiensis suspension(LC_(50)=0.185×10^(4) IU/L),Fatu B.thuringiensis suspension(LC_(50)=32.211×10^(4) IU/L),Nongbao Bio B.thuringiensis powder(LC_(50)=1590×10^(4) spores/L).[Conclusions]According to the three stages of tube rubbing,it is found that the control effects of Lujinwa B.thuringiensis powder and Meichongzhi B.bassiana powder are the best,and the results will provide technical support for the biological control of L.serricorne adults.

Occurrence Regularity and Life History of Cigarette Beetle Lasioderrma serricorne(Fabricius)in Tobacco Leaf Threshing and Redrying Workshop

[Objectives]The paper was to study the occurrence regularity and life history of cigarette beetle Lasioderrma serricorne(Fabricius)in tobacco leaf threshing and redrying workshop.[Methods]With the tobacco leaf threshing and redrying workshop as the survey site,the occurrence regularity of L.serricorne was investigated,and the life history table was inferred according to its biological characteristics.The temperature,humidity and duration of tobacco leaf threshing and redrying were simulated in the laboratory to study the survival rate of all states of L.serricorne in this environment.[Results]The lifecycle of L.serricorne in tobacco leaf threshing and redrying workshop was:the overwintering generation pupated in late February;the pupa began to emerge in early March,and reached its peak in late March.The first-generation eggs started hatching in late March,pupated in late May,emerged in early June,and reached the peak eclosion of the first-generation adults in mid-July.The second-generation eggs began to hatch in late July,pupated in mid-August,emerged in late August,and reached the peak eclosion of the second-generation adults in mid-September.The third-generation eggs began to hatch in mid-September;most of the larvae began to overwinter,some pupated in mid-November and survived the winter as pupae,and some pupae emerged to adults.The survival test results of different states of L.serricorne under simulated temperature,humidity and duration in the tobacco leaf threshing and redrying process showed that the mortality rates of eggs in simulated 1,2 and 3 conditions were about 51.22%,90.24% and 100%,and the mortalities of larvae in simulated 1,2 and 3 conditions were about 18.30%,81.25%and 100%,respectively.The mortalities of pupae in simulated 1,2 and 3 conditions were about 69.39%,100% and 100%,and the mortalities of adults in simulated 1,2 and 3 conditions were about 100%,100% and 100%,respectively.[Conclusions]L.serricorne of different states can be killed by appropriately raising the temperature during threshing and redrying.

DESTINY-Breast04:Calm Thinking on the HER2-low

The DESTINY-Breast04(DB-04)trial is a phaseⅢclinical trial that examined the efficacy of trastuzumab deruxtecan(T-DXd),an anti-HER2-antibody drug,in patients with low HER2 expression(HER2-low)advanced breast cancer.The study enrolled patients with HER2-low,unresectable,and/or recurrent metastatic breast cancer(mBC)who were resistant to previous endocrine therapy and had received one or two previous lines of chemotherapy.Among the 557 enrolled patients,494(88.7%)patients had hormone receptor-positive(HR+)mBC and 63(11.3%)patients had hormone receptor-negative(HR−)mBC.