Dynamics of module structures on Arundinella hirta populations in Songnen Plains of China

2015 ◽  
Vol 35 (8) ◽  
Author(s):  
李程程 LI Chengcheng ◽  
李海燕 LI Haiyan ◽  
杨允菲 YANG Yunfei
Keyword(s):  
Arundinella Hirta ◽  
Module Structures

scholarly journals Cycle and flow trusses in directed networks

2016 ◽  
Vol 3 (11) ◽  
pp. 160270 ◽  
Author(s):  
Taro Takaguchi ◽  
Yuichi Yoshida
Keyword(s):  
Truss Structures ◽  
Directed Network ◽  
Unified Framework ◽  
Directed Networks ◽  
Research Fields ◽  
Wide Range ◽  
Definition Of ◽  
Information Finding ◽  
Empirical Networks ◽  
Module Structures

When we represent real-world systems as networks, the directions of links often convey valuable information. Finding module structures that respect link directions is one of the most important tasks for analysing directed networks. Although many notions of a directed module have been proposed, no consensus has been reached. This lack of consensus results partly because there might exist distinct types of modules in a single directed network, whereas most previous studies focused on an independent criterion for modules. To address this issue, we propose a generic notion of the so-called truss structures in directed networks. Our definition of truss is able to extract two distinct types of trusses, named the cycle truss and the flow truss, from a unified framework. By applying the method for finding trusses to empirical networks obtained from a wide range of research fields, we find that most real networks contain both cycle and flow trusses. In addition, the abundance of (and the overlap between) the two types of trusses may be useful to characterize module structures in a wide variety of empirical networks. Our findings shed light on the importance of simultaneously considering different types of modules in directed networks.

Structure Design and Analysis for the Spacecraft On-Orbit Replacement Unit (ORU)

2013 ◽  
Vol 437 ◽  
pp. 449-453 ◽  
Author(s):  
Xi Zhai ◽  
Xin Hong Li ◽  
Si Yin Zhou
Keyword(s):  
Complex Structure ◽  
Structure Design ◽  
Module Structure ◽  
Assembly Technology ◽  
Universal Structure ◽  
Module Structures

By using on-orbit replacement and assembly technology, some fresh ideas and methods for the design, produce and application of spacecraft were put forward. Universal structure is one of the most basic requirements of On-Orbit replacement, assembly. Module structure must obey the rules of the Operationally Responsive Space (ORS). According to the degree of spacecraft module division, two module structures were proposed, and the complex structure was analyzed to verify the correctness of it.

scholarly journals Factorization of the canonical bases for higher-level Fock spaces

2011 ◽  
Vol 55 (1) ◽  
pp. 23-51 ◽  
Author(s):  
Susumu Ariki ◽  
Nicolas Jacon ◽  
Cédric Lecouvey
Keyword(s):  
Fock Space ◽  
Fock Spaces ◽  
Transition Matrices ◽  
Canonical Bases ◽  
Highest Weight ◽  
Highest Weight Modules ◽  
Graphic Module ◽  
Module Structures ◽  
Weight Modules

AbstractThe level l Fock space admits canonical bases $\mathcal{G}_{e}$ and $\smash{\mathcal{G}_{\infty}}$. They correspond to $\smash{\mathcal{U}_{v}(\widehat{\mathfrak{sl}}_{e})}$ and $\mathcal{U}_{v}({\mathfrak{sl}}_{\infty})$-module structures. We establish that the transition matrices relating these two bases are unitriangular with coefficients in ℕ[v]. Restriction to the highest-weight modules generated by the empty l-partition then gives a natural quantization of a theorem by Geck and Rouquier on the factorization of decomposition matrices which are associated to Ariki–Koike algebras.

scholarly journals Twisted Invariant Theory for Reflection Groups

2006 ◽  
Vol 182 ◽  
pp. 135-170 ◽  
Author(s):  
C. Bonnafé ◽  
G. I. Lehrer ◽  
J. Michel
Keyword(s):  
Invariant Theory ◽  
Regular Element ◽  
Central Element ◽  
Reflection Group ◽  
General Criterion ◽  
Coordinate Ring ◽  
Reflection Groups ◽  
Complex Vector ◽  
Finite Reflection Group ◽  
Module Structures

AbstractLet G be a finite reflection group acting in a complex vector space V = ℂr, whose coordinate ring will be denoted by S. Any element γ ∈ GL(V) which normalises G acts on the ring SG of G-invariants. We attach invariants of the coset Gγ to this action, and show that if G′ is a parabolic subgroup of G, also normalised by γ, the invariants attaching to G′γ are essentially the same as those of Gγ. Four applications are given. First, we give a generalisation of a result of Springer-Stembridge which relates the module structures of the coinvariant algebras of G and G′ and secondly, we give a general criterion for an element of Gγ to be regular (in Springer’s sense) in invariant-theoretic terms, and use it to prove that up to a central element, all reflection cosets contain a regular element. Third, we prove the existence in any well-generated group, of analogues of Coxeter elements of the real reflection groups. Finally, we apply the analysis to quotients of G which are themselves reflection groups.

scholarly journals Quantitative Trait Module-Based Genetic Analysis of Alzheimer’s Disease

2019 ◽  
Vol 20 (23) ◽  
pp. 5912
Author(s):  
Shaoxun Yuan ◽  
Haitao Li ◽  
Jianming Xie ◽  
Xiao Sun
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Medial Temporal Lobe ◽  
Interactive Effect ◽  
Brain Structures ◽  
Material Transport ◽  
Subcortical Structures ◽  
Main Effect ◽  
System Module ◽  
Module Structures

The pathological features of Alzheimer’s Disease (AD) first appear in the medial temporal lobe and then in other brain structures with the development of the disease. In this work, we investigated the association between genetic loci and subcortical structure volumes of AD on 393 samples in the Alzheimer’s Disease Neuroimaging Initiative (ADNI) cohort. Brain subcortical structures were clustered into modules using Pearson’s correlation coefficient of volumes across all samples. Module volumes were used as quantitative traits to identify not only the main effect loci but also the interactive effect loci for each module. Thirty-five subcortical structures were clustered into five modules, each corresponding to a particular brain structure/area, including the limbic system (module I), the corpus callosum (module II), thalamus–cerebellum–brainstem–pallidum (module III), the basal ganglia neostriatum (module IV), and the ventricular system (module V). Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment results indicate that the gene annotations of the five modules were distinct, with few overlaps between different modules. We identified several main effect loci and interactive effect loci for each module. All these loci are related to the function of module structures and basic biological processes such as material transport and signal transduction.

Comparison of photosynthetic carbon reduction (Kranz) cells having different ontogenetic origins in the C4 NADP – malic enzyme grass Arundinella hirta

1990 ◽  
Vol 68 (6) ◽  
pp. 1222-1232 ◽  
Author(s):  
Nancy G. Dengler ◽  
Ronald E. Dengler ◽  
Douglas J. Grenville
Keyword(s):  
Cell Walls ◽  
Vascular Tissue ◽  
Cell Types ◽  
Bundle Sheath ◽  
Carbon Reduction ◽  
Bundle Sheath Cells ◽  
Photosynthetic Carbon ◽  
Arundinella Hirta ◽  
Photosynthetic Carbon Reduction ◽  
Sheath Cells

The C4 grass Arundinella hirta is characterized by unusual leaf blade anatomy: photosynthetic carbon reduction takes place both within the chlorenchymatous bundle sheath cells of the longitudinal veins and within longitudinal strands of "distinctive cells" that form part of the leaf mesophyll and are often completely isolated from vascular tissue. Although they are equivalent physiologically, these two cell types have different ontogenetic origins: bundle sheath cells are delimited from procambium early in leaf development, whereas distinctive cells differentiate from ground meristem at a later developmental stage. Although the two cell types share numerous cytological features (large chloroplasts with reduced grana, thick cell walls with a suberin lamella), we also found significant differences in cell lengths, length to width ratios, cell cross-sectional areas, organelle numbers per cell cross section, phenol content of the cell walls, and numbers of pit fields in the longitudinal cell walls. The size and shape of bundle sheath cells are likely a direct consequence of procambial origin. The thicker walls of bundle sheath cells (in major veins) and their greater lignification may reflect the inductive effect of cell differentiation in the proximity of sclerenchyma and vascular tissues. Differences between major and minor vein bundle sheath cells may reflect differences in the timing of initiation of procambial strands. Our analysis of cell wall characteristics has also shown the presence of numerous primary pit fields in the transverse walls between adjacent distinctive cells in a file; plasmodesmata in these pit fields form a pathway for longitudinal symplastic transport not previously known to exist.

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