Dataset Information

A crystal plasticity FEM study of through-thickness deformation and texture in a {112} <111> aluminium single crystal during accumulative roll-bonding.

ABSTRACT: In this study, a crystal plasticity finite element method (CPFEM) model was used to study the deformation behaviour in an aluminium single crystal (1 1 2)[1 1 -1] processed by accumulative roll-bonding (ARB) up to 9 cycles. The simulation followed the real ARB process based on the developed finite element model. The predicted through-thickness texture matches well with the experimental observations. The deformation behaviours, in terms of crystal rotation, shear strain and slip system activation, in the first and second cycles (conventional rolling) were unidirectional, but the deformation was altered after ARB was applied from the third cycle onwards. Such alteration was found to be caused by the thickness position change and deformation discontinuity at interfaces, which were investigated in detail. The role that interfaces play became dominant over thickness position change as increasing ARB cycles.

SUBMITTER: Wang H

PROVIDER: S-EPMC6399260 | biostudies-literature | 2019 Mar

REPOSITORIES: biostudies-literature

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A crystal plasticity FEM study of through-thickness deformation and texture in a {112} <111> aluminium single crystal during accumulative roll-bonding.

Wang Hui H Lu Cheng C Tieu Kiet K Deng Guanyu G Wei Peitang P Liu Yu Y

Scientific reports 20190304 1

In this study, a crystal plasticity finite element method (CPFEM) model was used to study the deformation behaviour in an aluminium single crystal (1 1 2)[1 1 -1] processed by accumulative roll-bonding (ARB) up to 9 cycles. The simulation followed the real ARB process based on the developed finite element model. The predicted through-thickness texture matches well with the experimental observations. The deformation behaviours, in terms of crystal rotation, shear strain and slip system activation ...[more]

PMID: 30833615

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Project description:Wheat cultivars ‘TAM 111’ and ‘TAM 112’ have been dominantly grown in the Southern U.S. Great Plains for many years due to their excellent, yet variable, drought tolerance. To identify the molecular basis and genetic control of drought tolerance in these two landmark cultivars, RNA-seq analysis was conducted to compare gene expression difference in flag leaves under fully irrigated (wet) and water deficient (dry) conditions. Of the 122,017 gene sequences assembled, 2,254 genes showed significantly altered expression patterns under dry and wet conditions in the two cultivars. TAM 111 had 593 and 1,532 dry-wet differentially expressed genes (DEGs), and TAM 112 had 777 and 1,670 at heading and grain-filling stages, respectively. The two cultivars have 1,214 (53.9%) dry-wet DEGs in common, which agreed with their excellent adaption to drought, but 438 and 602 dry-wet DEGs were respectively shown only in TAM 111 and TAM 112 suggested that each may have a specific mechanism to cope with drought. Annotation of all 2,254 genes with dry-wet expression difference found 1,855 have functions related to biosynthesis, stress responses, defense responses, transcription factors and cellular components related to ion or protein transportation and signal transduction. Comparing hierarchical structure of biological processes, molecule functions and cellular components revealed the significant regulation differences between TAM 111 and TAM 112, particularly for genes of phosphorylation and adenyl ribonucleotide binding, and proteins located in nucleus and plasma membrane. Comparing gene expressions involved in responses to stresses of water deprivation, heat and oxidative, ABA-induced signal pathway and transcription regulation found TAM 112 have more specific dry-wet DEGs than TAM 111 with most of them up-regulated, indicating that TAM 112 is more active than TAM 111 in response to drought. In addition, 399 dry-wet DEGs with unknown functions included 258 genes encoding predicted uncharacterized proteins and 141 unannotated genes with no similar sequences identified in the databases. These may represent novel genes related to drought response in TAM 111 or TAM 112. This research thus revealed different drought-tolerance mechanisms in TAM 111 and TAM 112 and identified useful drought tolerance genes for wheat adaption.

Project description:Wheat cultivars 'TAM 111' and 'TAM 112' have been dominantly grown in the Southern U.S. Great Plains for many years due to their high yield and drought tolerance. To identify the molecular basis and genetic control of drought tolerance in these two landmark cultivars, RNA-seq analysis was conducted to compare gene expression difference in flag leaves under fully irrigated (wet) and water deficient (dry) conditions. A total of 2254 genes showed significantly altered expression patterns under dry and wet conditions in the two cultivars. TAM 111 had 593 and 1532 dry-wet differentially expressed genes (DEGs), and TAM 112 had 777 and 1670 at heading and grain-filling stages, respectively. The two cultivars have 1214 (53.9%) dry-wet DEGs in common, which agreed with their excellent adaption to drought, but 438 and 602 dry-wet DEGs were respectively shown only in TAM 111 and TAM 112 suggested that each has a specific mechanism to cope with drought. Annotations of all 2254 genes showed 1855 have functions related to biosynthesis, stress responses, defense responses, transcription factors and cellular components related to ion or protein transportation and signal transduction. Comparing hierarchical structure of biological processes, molecule functions and cellular components revealed the significant regulation differences between TAM 111 and TAM 112, particularly for genes of phosphorylation and adenyl ribonucleotide binding, and proteins located in nucleus and plasma membrane. TAM 112 showed more active than TAM 111 in response to drought and carried more specific genes with most of them were up-regulated in responses to stresses of water deprivation, heat and oxidative, ABA-induced signal pathway and transcription regulation. In addition, 258 genes encoding predicted uncharacterized proteins and 141 unannotated genes with no similar sequences identified in the databases may represent novel genes related to drought response in TAM 111 or TAM 112. This research thus revealed different drought-tolerance mechanisms in TAM 111 and TAM 112 and identified useful drought tolerance genes for wheat adaption. Data of gene sequence and expression regulation from this study also provided useful information of annotating novel genes associated with drought tolerance in the wheat genome.

Dataset Information

A crystal plasticity FEM study of through-thickness deformation and texture in a {112} <111> aluminium single crystal during accumulative roll-bonding.

Publications

A crystal plasticity FEM study of through-thickness deformation and texture in a {112} <111> aluminium single crystal during accumulative roll-bonding.

Similar Datasets

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