Projective Approximations

1984 ◽  
Vol 36 (1) ◽  
pp. 178-192 ◽  
Author(s):  
K. Varadarajan

Let R be an associative ring with 1 ≠ 0. Throughout we will be considering unitary left R-modules. Given a chain complex C over R, a free approximation of C is defined to be a free chain complex F over R together with an epimorphism τ:F → C of chain complexes with the property that H(τ):H(F) ≃ H(C). In Chapter 5, Section 2 of [3] it is proved that any chain complex C over Z has a free approximation τ:F → C. Moreover given a free approximation τ:F → C of C and any chain map f:F’ → C with F’ a free chain complex over Z, there exists a chain map φ:F’→ F with T O φ = f . Any two chain maps φ, ψ of F’ in F with T O φ = T O ψ are chain homotopic.

2009 ◽  
Vol 18 (09) ◽  
pp. 1227-1258
Author(s):  
JAE-WOOK CHUNG ◽  
XIAO-SONG LIN

In this paper, we introduce the notion of Reidemeister torsion for quasi-isomorphisms of based chain complexes over a field. We call a chain map a quasi-isomorphism if its induced homomorphism between homology is an isomorphism. Our notion of torsion generalizes the torsion of acyclic based chain complexes, and is a chain homotopy invariant on the collection of all quasi-isomorphisms from a based chain complex to another. It shares nice properties with torsion of acyclic based chain complexes, like multiplicativity and duality. We will further generalize our torsion to quasi-isomorphisms between free chain complexes over a ring under some mild condition. We anticipate that the study of torsion of quasi-isomorphisms will be fruitful in many directions, and in particular, in the study of links in 3-manifolds.


2020 ◽  
pp. 1-33
Author(s):  
ALBERTO CAVALLO

Abstract We introduce a generalization of the Lisca–Ozsváth–Stipsicz–Szabó Legendrian invariant ${\mathfrak L}$ to links in every rational homology sphere, using the collapsed version of link Floer homology. We represent a Legendrian link L in a contact 3-manifold ${(M,\xi)}$ with a diagram D, given by an open book decomposition of ${(M,\xi)}$ adapted to L, and we construct a chain complex ${cCFL^-(D)}$ with a special cycle in it denoted by ${\mathfrak L(D)}$ . Then, given two diagrams ${D_1}$ and ${D_2}$ which represent Legendrian isotopic links, we prove that there is a map between the corresponding chain complexes that induces an isomorphism in homology and sends ${\mathfrak L(D_1)}$ into ${\mathfrak L(D_2)}$ . Moreover, a connected sum formula is also proved and we use it to give some applications about non-loose Legendrian links; that are links such that the restriction of ${\xi}$ on their complement is tight.


2020 ◽  
Vol 4 (4) ◽  
pp. 455-480
Author(s):  
U. Bauer ◽  
H. Edelsbrunner ◽  
G. Jabłoński ◽  
M. Mrozek

Abstract We call a continuous self-map that reveals itself through a discrete set of point-value pairs a sampled dynamical system. Capturing the available information with chain maps on Delaunay complexes, we use persistent homology to quantify the evidence of recurrent behavior. We establish a sampling theorem to recover the eigenspaces of the endomorphism on homology induced by the self-map. Using a combinatorial gradient flow arising from the discrete Morse theory for Čech and Delaunay complexes, we construct a chain map to transform the problem from the natural but expensive Čech complexes to the computationally efficient Delaunay triangulations. The fast chain map algorithm has applications beyond dynamical systems.


2017 ◽  
Vol 57 (8) ◽  
pp. 1674
Author(s):  
M. J. Zamiri ◽  
R. Mehrabi ◽  
G. R. Kavoosi ◽  
H. Rajaei Sharifabadi

The present study was conducted to determine the relationship between the activity of mitochondrial respiratory chain complexes in pre- and post-slaughter muscle samples and residual feed intake (RFI) in Ghezel male lambs born as a result of random mating. The study was based on the hypothesis that random-bred lambs with lower feed (or higher) RFI have lower (or higher) respiratory chain-complex activity in muscle samples. Lambs (n = 30) were fed a diet consisting of 70% concentrate and 30% alfalfa hay during a 70-day period. Individual feed intake and average daily gain were recorded to calculate the RFI, feed-conversion ratio (FCR) and adjusted FCR (aFCR). On the basis of these calculations, the lambs were classified into low and high groups for RFI, with FCR and aFCR (n = 22) being one standard deviation above or below the means; this was corroborated by Student’s t-test (P < 0.01). At the end of the experiment, a 10-g biopsy sample was taken from the posterior side of the left femoral biceps. After 24 h, the lambs were slaughtered, and a sample from the posterior side of the right femoral biceps was dissected for determination of mitochondrial protein and respiratory chain-complex activities (Complexes I–V). The RFI was not correlated with the metabolic bodyweight and average daily gain, but was positively correlated (r = 0.56) with the average daily feed intake (P < 0.01); mean daily feed intake in the low-RFI group was 200 g less than that in the high-RFI group. The FCR and aFCR were not significantly (P > 0.05) correlated with average daily feed intake (r = 0.39 and r = 0.36 respectively), but showed a negative correlation (P < 0.01) with average daily gain (r = –0.73 and r = –0.76 respectively). Although very high negative correlations were recorded between the activities of all five respiratory-chain complexes and RFI in muscle samples obtained before (–0.91 to –0.97) and after (–0.92 to –0.97) slaughter, Complexes I and V showed small negative correlations (–0.40) with FCR or aFCR (P < 0.05). Enzyme activities of the respiratory-chain Complexes I, III and V were not significantly different between the pre- and post-slaughter biopsy samples; however, the enzyme activities of respiratory-chain Complexes II and IV were slightly higher in post-slaughter samples (P < 0.01). These results suggested that it may be possible to use the enzymatic activity of respiratory-chain complexes in muscle biopsy samples for screening of lambs for RFI, providing a useful procedure for genetic selection of lambs for this component of feed efficiency. These encouraging results need to be verified in further experiments using other sheep breeds and a larger number of lambs.


2013 ◽  
Vol 29 (0) ◽  
pp. 21-22 ◽  
Author(s):  
Masahiro MIKURIYA ◽  
Kazuya OUCHI ◽  
Yasutaka NAKANISHI ◽  
Daisuke YOSHIOKA ◽  
Hidekazu TANAKA ◽  
...  

2019 ◽  
Vol 150 (4) ◽  
pp. 1937-1964 ◽  
Author(s):  
Hua-Lin Huang ◽  
Zheyan Wan ◽  
Yu Ye

AbstractWe provide explicit and unified formulas for the cocycles of all degrees on the normalized bar resolutions of finite abelian groups. This is achieved by constructing a chain map from the normalized bar resolution to a Koszul-like resolution for any given finite abelian group. With a help of the obtained cocycle formulas, we determine all the braided linear Gr-categories and compute the Dijkgraaf–Witten Invariants of the n-torus for all n.


2008 ◽  
Vol 17 (01) ◽  
pp. 31-45 ◽  
Author(s):  
MARKO STOŠIĆ

For each graph and each positive integer n, we define a chain complex whose graded Euler characteristic is equal to an appropriate n-specialization of the dichromatic polynomial. This also gives a categorification of n-specializations of the Tutte polynomial of graphs. Also, for each graph and integer n ≤ 2, we define the different one-variable n-specializations of the dichromatic polynomial, and for each polynomial, we define graded chain complex whose graded Euler characteristic is equal to that polynomial. Furthermore, we explicitly categorify the specialization of the Tutte polynomial for graphs which corresponds to the Jones polynomial of the appropriate alternating link.


2012 ◽  
Vol 55 (1) ◽  
pp. 145-160 ◽  
Author(s):  
THOMAS HÜTTEMANN ◽  
DAVID QUINN

AbstractSuppose C is a bounded chain complex of finitely generated free modules over the Laurent polynomial ring L = R[x,x−1]. Then C is R-finitely dominated, i.e. homotopy equivalent over R to a bounded chain complex of finitely generated projective R-modules if and only if the two chain complexes C ⊗LR((x)) and C ⊗LR((x−1)) are acyclic, as has been proved by Ranicki (A. Ranicki, Finite domination and Novikov rings, Topology34(3) (1995), 619–632). Here R((x)) = R[[x]][x−1] and R((x−1)) = R[[x−1]][x] are rings of the formal Laurent series, also known as Novikov rings. In this paper, we prove a generalisation of this criterion which allows us to detect finite domination of bounded below chain complexes of projective modules over Laurent rings in several indeterminates.


Medicina ◽  
2010 ◽  
Vol 46 (10) ◽  
pp. 679
Author(s):  
Vida Gendvilienė ◽  
Irma Martišienė ◽  
Danguolė Zablockaitė ◽  
Jonas Jurevičius

The aim of the study was to investigate the effect of inhibitors of mitochondrial respiratory chain complexes I, III, and IV on the electromechanical activity in human myocardium. Material and methods. The experiments were performed on the human myocardial strips obtained from patients with heart failure (NYHA class III or IV) using a conventional method of registration of myocardial electromechanical activity. Under the perfusion with physiological Tyrode solution (control), contraction force (P) was 0.94±0.12 mN (n=16), relaxation time (t50) was 173.38±5.03 ms (n=15), action potential durations measured at 50% (AP50) and 90% (AP90) repolarization were 248.96±13.38 ms and 398.59±17.93 ms, respectively (n=13). Results. The inhibition of respiratory chain complex I by rotenone (3×10–5 M, the highest concentration applied) decreased contraction force of human myocardium to 48.99%±14.74% (n=3) (P<0.05); AP50, to 81.34%±15.81%; and AP90, to 87.28%±7.25% (n=3) (P>0.05) of control level, while relaxation time and resting tension remained almost unchanged. Antimycin A, an inhibitor of complex III, applied at the highest concentration (3×10–4 M) reduced P to 41.66%±8.8% (n=5) (P<0.001) and marginally increased t50 and decreased the durations of AP. Anoxia (3 mM Na2S2O4) that inhibits the activity of complex IV reduced the contraction force to 9.23%±3.56% (n=6) (P<0.001), AP50 and AP90 to 65.46%±9.95% and 71.07%±8.39% (n=5) (P<0.05) of control level, respectively; furthermore, the resting tension augmented (contracture developed). Conclusions. Our results show that the inhibition of respiratory chain complex IV had the strongest inhibitory effect on the electromechanical activity of failing human myocardium.


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