Populus Tomentosa(포풀루스 토멘토사)란 무엇입니까?
Populus Tomentosa 포풀루스 토멘토사 - Here we performed a comprehensive analysis of morphological observations, transcriptome profiles, the DNA methylome, and miRNAs of the cambium in Populus tomentosa during the transition from dormancy to activation. [1] Herein, we propose the adsorption-pyrolysis-doping strategy to tailor the content of C−S−C/S−C species and pore sizes of biomass-derived N, S-doped porous carbon catalyst from populus tomentosa to achieve the activity and selectivity of H2O2 electrosynthesis and develop a 3D printed revolving roller-compacted triboelectric nanogenerator (RRC-TENG) as an electric supply with instantaneous short circuit current of 285 μA, open circuit voltage of 500 V, transferred charge of 1. [2] In this study, we constructed a FOX library from the Chinese white poplar, Populus tomentosa. [3] Through a comparative analysis of gene regulation in response to heat in Arabidopsis thaliana, Populus tomentosa and N. [4] Through a comparative analysis of gene regulation in response to heat in Arabidopsis thaliana, Populus tomentosa and N. [5] Here, we employed Illumina sequencing technology to assess how miRNA and messenger RNA (mRNA) populations vary in the Chinese white poplar (Populus tomentosa) during a leaf black spot fungus (Marssonina brunnea) infection. [6] The resistance to growth of molds for MACu modified wood (Populus tomentosa) was measured according to ASTM D3273-16. [7] Based on the field survey, forest resources data and the measured standard emission factors, the Guenther model developed in 1993 (G93) was applied in this paper to estimate the emission of BVOCs from several dominant forest species ( Platycladus orientalis , Quercus variabilis , Betula platyphylla , Populus tomentosa , Pinus tabuliformis , Robinia pseudoacacia , Ulmus pumila , Salix babylonica and Larix gmelinii ) in the Jing-Jin-Ji area in 2017. [8] In the present study, applying the strategy of detecting hDNA by constructing populations from inhibited post-meiotic segregation, two hybrid triploid populations were constructed from two maternal parents inPopulus tomentosa by inhibiting post-meiotic segregation. [9] Here, we use Illumina sequencing to assess how sRNA populations vary in the Chinese white poplar (Populus tomentosa) during a rust fungus (Melampsora larici-populina) infection. [10] To elucidate the phenotypic and molecular effects of polyploidization, we obtained hexaploids by applying colchicine to a triploid clone (Populus tomentosa × P. [11] A high‐performance liquid chromatography (HPLC) fingerprint method with multivariate statistical analyses was applied to discriminate the male and female barks of Populus tomentosa for the first time. [12] Using RNA sequencing, we obtained a high-resolution temporal profile of gene expression during autumn leaf senescence in poplar (Populus tomentosa). [13] By investigating sap flow in 14 lateral roots (LRs) randomly selected from trees of a Chinese white poplar (Populus tomentosa) plantation receiving three levels of irrigation, an unknown root water transport mode of simultaneous daytime bi-directional water flow was discovered. [14] lannesiana were found weak correlation with O3 and SOA generation, while Salix matsudana, Populus tomentosa and Salix matsudana f pendula were strongly related. [15] Enzymatic assay of Populus tomentosa (Popto) CSE1, -2 and -12 showed that PoptoCSE1 and -2 kept CSE activity. [16] PeWRKY31 is a zinc-finger C 2 H 2 type-II WRKY TF that is closely related to WRKY TFs of Populus tomentosa , and localizes to the nucleus. [17] Then plantation poplar wood (Populus tomentosa) was impregnated and modified with them. [18] (BY), Salix matsudana Koidz (LS), Populus tomentosa (YS), Sophora japonica Linn (GH) and Platycladus orientalis (L. [19] In field experiments, we recorded stem water content and freeze–thaw data of Pachira glabra, Populus tomentosa, and Lagerstroemia indica during an overwintering period. [20] In this study, 11 members of the XTH gene family were cloned from Populus tomentosa. [21] Four wood species including Masson pine (Pinus massoniana), Chinese fir (Cunninghamia lanceolata), poplar (Populus tomentosa) and ayous (Triplochiton scleroxylon) were studied. [22] Here, we report that a microRNA, miR6443, specifically regulates S lignin biosynthesis during stem development in Populus tomentosa. [23] The divergence of CCRs and CCR-like sequences in Populus tomentosa, Panicum virgatum, Oryza sativa, and Selaginella moellendorffii suggests that NWYCY is not efficient for CCR recognition. [24] In this study, we used small RNA (sRNA) sequencing to build four libraries derived from shoot tips and mature leaf tissues of Populus tomentosa, and identified 99 known miRNA families. [25] In this study, we isolated an ABC transporter gene PtoABCG36 from Populus tomentosa. [26] DNA methylation and long non-coding RNAs (lncRNAs) regulate plant growth and development, but their relationship and effect on responses to the auxin phytohormone indole-3-acetic acid (IAA) remain largely unknown, particularly in woody plants such as poplar (Populus tomentosa). [27] In this study, the microstructure and mechanical properties of poplar (Populus tomentosa) catkin fibers (PCFs) were investigated using field emission scanning electron microscope, atomic force microscopy (AFM), X-ray diffraction, and nanoindentation methods. [28] To expand the applications of low-density wood, solid white poplar (Populus tomentosa) wood with a moisture content of 10. [29] We isolated an R2R3-MYB transcription factor MYB6 from Populus tomentosa and determined that it was expressed predominately in young leaves. [30] Females were capable of developing eggs when provided Acer rubrum, but not Populus deltoides or Populus tomentosa. [31] Here, we identified an Aux/INDOLE-3-ACETIC ACID 9 (IAA9)-AUXIN RESPONSE FACTOR 5 (ARF5) module in Populus tomentosa as a key mediator of auxin signaling to control early developing xylem development. [32] Populus tomentosa is a major industrial tree species used for timber and pulp manufacturing in northern China. [33] X-ray computed tomography (X-CT) technology was used to analyze the difference in the CT number of the heartwood and sapwood of Chinese white poplar (Populus tomentosa) and Masson pine (Pinus massoniana) under different MC. [34] To evaluate the roles of expansin in response to different environmental stress conditions, the expansin gene PttEXPA8 from Populus tomentosa was transformed into tobacco. [35] In this study, we isolated the single-copy gene PtSS3 from the SS gene family of Populus tomentosa and analyzed its structure. [36] The effects of chemical pretreatment on the purification of poplar (Populus tomentosa) catkin fiber and the effect of ultrasonic time for the microfibrillarization of poplar catkin fiber (PCF) were studied. [37] Populus tomentosa, of section Populus, is distributed mainly in northern China. [38] Expression of PtoNF-Y was analyzed during floral bud development in Populus tomentosa. [39] In this study, we used the PacBio SEQUEL software to determine that the cp genome of Populus tomentosa has a length of 156,558 bp including a long single-copy region (84,717 bp), a small single-copy region (16,555 bp), and a pair of inverted repeat regions (27,643 bp). [40] Here, we used association genetics (additive, dominant and epistasis) and expression quantitative trait nucleotide (eQTN) mapping to decipher the genetic networks for tree growth and wood properties in 435 unrelated individuals of Populus tomentosa. [41] We used two Populus populations: a linkage mapping population comprising a full‐sib family of 1,200 progeny and an association mapping panel comprising 435 unrelated individuals from nearly the entire natural range of Populus tomentosa. [42] It is difficult for wood fibers/high density polyethylene (WF/HDPE) composites to laminate with poplar (Populus tomentosa) wood veneer due to its nonpolar and imporous surface. [43] In this study, a total of 110 allotriploid individuals from two cross combinations who shared only one male parent were obtained by chromosome doubling of megaspore via high temperature treatment in Populus tomentosa. [44] In this paper we examine the biomechanical effects on slope stability of the roots of Populus tomentosa, Robinia pseudoacacia and Olea europaea in a geohazard-prone region in China. [45]여기에서 우리는 휴면에서 활성화로 전환하는 동안 Populus tomentosa의 형성층의 형태학적 관찰, transcriptome 프로필, DNA methylome 및 miRNA에 대한 포괄적인 분석을 수행했습니다. [1] 여기에서, 우리는 활성 및 선택성을 달성하기 위해 populus tomentosa에서 바이오매스 유래 N, S-도핑된 다공성 탄소 촉매의 C-S-C/S-C 종의 함량 및 기공 크기를 조정하기 위한 흡착-열분해-도핑 전략을 제안합니다. 285μA의 순간 단락 전류, 500V의 개방 회로 전압, 1의 전송된 전하를 갖는 전기 공급 장치로 3D 인쇄된 회전 롤러 압축 마찰전기 나노발전기(RRC-TENG)를 개발했습니다. [2] 이 연구에서 우리는 중국 백합, Populus tomentosa에서 FOX 라이브러리를 구성했습니다. [3] Arabidopsis thaliana, Populus tomentosa 및 N. [4] Arabidopsis thaliana, Populus tomentosa 및 N. [5] 여기에서 우리는 Illumina 시퀀싱 기술을 사용하여 잎 검은 반점 균류(Marssonina brunnea) 감염 동안 중국 백합(Populus tomentosa)에서 miRNA 및 메신저 RNA(mRNA) 개체군이 어떻게 변하는지 평가했습니다. [6] MACu 변형 목재(Populus tomentosa)에 대한 곰팡이의 성장 저항성은 ASTM D3273-16에 따라 측정되었습니다. [7] 현장 조사, 산림 자원 데이터 및 측정된 표준 배출 계수를 기반으로 1993년에 개발된 Guenther 모델(G93)을 본 논문에서 적용하여 여러 주요 산림 종( Platycladus orientalis , Quercus variabilis , Betula platyphylla , Populus tomentosa , Pinus tabuliformis , Robinia pseudoacacia , Ulmus pumila , Salix babylonica 및 Larix gmelinii ) 2017년 Jing-Jin-Ji 지역. [8] 본 연구에서는 억제된 감수분열 후 분리로부터 개체군을 구성하여 hDNA를 검출하는 전략을 적용하여 감수분열 후 분리를 억제하여 토멘토사에서 2개의 모친으로부터 2개의 잡종 삼배체 개체군을 구성했습니다. [9] 여기에서 우리는 Illumina 시퀀싱을 사용하여 녹병균(Melampsora larici-populina) 감염 동안 중국 백양목(Populus tomentosa)에서 sRNA 개체군이 어떻게 다른지 평가합니다. [10] 배수체화의 표현형 및 분자적 효과를 설명하기 위해 우리는 삼배체 클론(Populus tomentosa × P)에 콜히친을 적용하여 6배체를 얻었다. [11] 다변량 통계 분석을 통한 고성능 액체 크로마토그래피(HPLC) 지문법을 최초로 적용하여 포풀루스 토멘토사의 암수 수피를 구별했습니다. [12] RNA 시퀀싱을 사용하여 우리는 포플러(Populus tomentosa)의 가을 잎 노화 동안 유전자 발현의 고해상도 시간적 프로파일을 얻었습니다. [13] 세 가지 수준의 관개를 받는 중국 백양나무(Populus tomentosa) 농장의 나무에서 무작위로 선택된 14개의 측근(LR)에서 수액 흐름을 조사하여 동시 주간 양방향 물 흐름의 알려지지 않은 뿌리 물 수송 모드를 발견했습니다. [14] lannesiana는 O3 및 SOA 생성과 약한 상관관계가 있는 반면 Salix matsudana, Populus tomentosa 및 Salix matsudana f pendula는 강한 상관관계가 있는 것으로 나타났습니다. [15] Populus tomentosa (Popto) CSE1, -2 및 -12의 효소 분석은 PoptoCSE1 및 -2가 CSE 활성을 유지함을 보여주었습니다. [16] PeWRKY31은 징크핑거 C 2 H 2 type-II WRKY TF로 Populus tomentosa의 WRKY TF와 밀접하게 관련되어 있으며 핵에 국한되어 있습니다. [17] 그런 다음 재배 포플러 나무(Populus tomentosa)를 함침하고 수정했습니다. [18] (BY), Salix matsudana Koidz (LS), Populus tomentosa (YS), Sophora japonica Linn (GH) 및 Platycladus orientalis (L. [19] 현장 실험에서 우리는 월동 기간 동안 Pachira glabra, Populus tomentosa 및 Lagerstroemia indica의 줄기 수분 함량 및 동결-해동 데이터를 기록했습니다. [20] 이 연구에서 XTH 유전자 패밀리의 11개 구성원이 Populus tomentosa에서 복제되었습니다.