scholarly journals Clonal selection in S0 and S1 peach trees evaluated in a subtropical environment

2021 ◽  
Vol 21 (1) ◽  
Author(s):  
José Osmar da Costa e Silva ◽  
Claudio Horst Bruckner ◽  
Pedro Crescêncio Souza Carneiro ◽  
Marcos Deon Vilela de Resende ◽  
Rodrigo Silva Alves ◽  
...  
2011 ◽  
Vol 33 (7) ◽  
pp. 1561-1567 ◽  
Author(s):  
Xiao-fei Wang ◽  
Yue-bing Chen ◽  
Xi Zhang ◽  
Quan Zhang ◽  
Chao-jing Tang

HortScience ◽  
1998 ◽  
Vol 33 (3) ◽  
pp. 541b-541
Author(s):  
Rita Giuliani ◽  
James A. Flore

Potted peach trees grown outdoors during the 1997 season were subjected to drought and subsequent rewatering to evaluate their dynamic response to soil water content. The investigation was primarily focused on the early detection of plant water stress to prevent negative effects on the growth. Leaf chlorophyll fluorescence and canopy temperature estimates (by infra-red thermometry) were conducted. Drought effect on physiological processes were detected through by estimates of canopy development rate, leaf gas-exchange measurements; while leaf water potential was measured to characterize plant water status. A decrease in the canopy's development rate was found 1 week after irrigation was stopped, which also coincided with a more-negative leaf water potential, whereas a decrease of the gas-exchange activities occurred several days later. No significant differences between the stressed and control plants were recorded by the chlorophyll fluorescence parameters (Fo, Fm, Fv and the ratio Fv/Fm), whereas the infra-red estimates of canopy temperature detected a slight increase of the canopy surface temperature (connected to the change of leaf energy balance and in relation to partial stomatal closure) on the non-irrigated plants 1 week after the beginning of the trial. The use of infra-red thermometry for early detection of water shortage is discussed.


HortScience ◽  
1998 ◽  
Vol 33 (3) ◽  
pp. 452c-452 ◽  
Author(s):  
Schuyler D. Seeley ◽  
Raymundo Rojas-Martinez ◽  
James Frisby

Mature peach trees in pots were treated with nighttime temperatures of –3, 6, 12, and 18 °C for 16 h and a daytime temperature of 20 °C for 8 h until the leaves abscised in the colder treatments. The trees were then chilled at 6 °C for 40 to 70 days. Trees were removed from chilling at 40, 50, 60, and 70 days and placed in a 20 °C greenhouse under increasing daylength, spring conditions. Anthesis was faster and shoot length increased with longer chilling treatments. Trees exposed to –3 °C pretreatment flowered and grew best with 40 days of chilling. However, they did not flower faster or grow better than the other treatments with longer chilling times. There was no difference in flowering or growth between the 6 and 12 °C pretreatments. The 18 °C pretreatment resulted in slower flowering and very little growth after 40 and 50 days of chilling, but growth was comparable to other treatments after 70 days of chilling.


2018 ◽  
Vol 7 (2) ◽  
pp. 99-114
Author(s):  
Abdaallah El-Kharafen ◽  
Hany El-Alakmy ◽  
Roqia Ahmed ◽  
Mohamed Sourour ◽  
Mohamed ElDeep

Blood ◽  
2019 ◽  
Vol 133 (13) ◽  
pp. 1436-1445 ◽  
Author(s):  
Jyoti Nangalia ◽  
Emily Mitchell ◽  
Anthony R. Green

Abstract Interrogation of hematopoietic tissue at the clonal level has a rich history spanning over 50 years, and has provided critical insights into both normal and malignant hematopoiesis. Characterization of chromosomes identified some of the first genetic links to cancer with the discovery of chromosomal translocations in association with many hematological neoplasms. The unique accessibility of hematopoietic tissue and the ability to clonally expand hematopoietic progenitors in vitro has provided fundamental insights into the cellular hierarchy of normal hematopoiesis, as well as the functional impact of driver mutations in disease. Transplantation assays in murine models have enabled cellular assessment of the functional consequences of somatic mutations in vivo. Most recently, next-generation sequencing–based assays have shown great promise in allowing multi-“omic” characterization of single cells. Here, we review how clonal approaches have advanced our understanding of disease development, focusing on the acquisition of somatic mutations, clonal selection, driver mutation cooperation, and tumor evolution.


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