Cellular approximation theorem explained

In algebraic topology, the cellular approximation theorem states that a map between CW-complexes can always be taken to be of a specific type. Concretely, if X and Y are CW-complexes, and f : X → Y is a continuous map, then f is said to be cellular, if f takes the n-skeleton of X to the n-skeleton of Y for all n, i.e. if

f(X ^{n)\subseteq} Y ^{n} for all n. The content of the cellular approximation theorem is then that any continuous map f : X → Y between CW-complexes X and Y is homotopic to a cellular map, and if f is already cellular on a subcomplex A of X, then we can furthermore choose the homotopy to be stationary on A. From an algebraic topological viewpoint, any map between CW-complexes can thus be taken to be cellular.

Idea of proof

The proof can be given by induction after n, with the statement that f is cellular on the skeleton Xⁿ. For the base case n=0, notice that every path-component of Y must contain a 0-cell. The image under f of a 0-cell of X can thus be connected to a 0-cell of Y by a path, but this gives a homotopy from f to a map which is cellular on the 0-skeleton of X.

Assume inductively that f is cellular on the (n - 1)-skeleton of X, and let eⁿ be an n-cell of X. The closure of eⁿ is compact in X, being the image of the characteristic map of the cell, and hence the image of the closure of eⁿ under f is also compact in Y. Then it is a general result of CW-complexes that any compact subspace of a CW-complex meets (that is, intersects non-trivially) only finitely many cells of the complex. Thus f(eⁿ) meets at most finitely many cells of Y, so we can take

e ^{k\subseteq} Y to be a cell of highest dimension meeting f(eⁿ). If k\leq n , the map f is already cellular on eⁿ, since in this case only cells of the n-skeleton of Y meets f(eⁿ), so we may assume that k > n. It is then a technical, non-trivial result (see Hatcher) that the restriction of f to X ^{n-1} \cup e ^{n} can be homotoped relative to X^n-1 to a map missing a point p ∈ e^k. Since Y^k -  deformation retracts onto the subspace Y^k-e^k, we can further homotope the restriction of f to X ^{n-1} \cup e ^{n} to a map, say, g, with the property that g(eⁿ) misses the cell e^k of Y, still relative to X^n-1. Since f(eⁿ) met only finitely many cells of Y to begin with, we can repeat this process finitely many times to make f(e ^{n)} miss all cells of Y of dimension larger than n.

We repeat this process for every n-cell of X, fixing cells of the subcomplex A on which f is already cellular, and we thus obtain a homotopy (relative to the (n - 1)-skeleton of X and the n-cells of A) of the restriction of f to Xⁿ to a map cellular on all cells of X of dimension at most n. Using then the homotopy extension property to extend this to a homotopy on all of X, and patching these homotopies together, will finish the proof. For details, consult Hatcher.

Applications

Some homotopy groups

The cellular approximation theorem can be used to immediately calculate some homotopy groups. In particular, if

n<k, then \pi ^{k) =0 .} _{n(S} Give S ^{n} and S ^{k} their canonical CW-structure, with one 0-cell each, and with one -cell for S ^{n} and one -cell for S ^{k.} Any base-point preserving map f\colon S ^{n} \to S ^{k} is then homotopic to a map whose image lies in the -skeleton of S ^{k,} which consists of the base point only. That is, any such map is nullhomotopic.

Cellular approximation for pairs

Let f:(X,A)→(Y,B) be a map of CW-pairs, that is, f is a map from X to Y, and the image of

A\subseteq X under f sits inside B. Then f is homotopic to a cellular map (X,A)→(Y,B). To see this, restrict f to A and use cellular approximation to obtain a homotopy of f to a cellular map on A. Use the homotopy extension property to extend this homotopy to all of X, and apply cellular approximation again to obtain a map cellular on X, but without violating the cellular property on A.

As a consequence, we have that a CW-pair (X,A) is n-connected, if all cells of

X - A have dimension strictly greater than n: If i\leq n , then any map (D ^{i,\partial} D ^{i)} →(X,A) is homotopic to a cellular map of pairs, and since the n-skeleton of X sits inside A, any such map is homotopic to a map whose image is in A, and hence it is 0 in the relative homotopy group \pi _{i(X,A)} .
We have in particular that (X,X ^{n)} is n-connected, so it follows from the long exact sequence of homotopy groups for the pair (X,X ^{n)} that we have isomorphisms \pi ^{n)} _{i(X} →\pi _{i(X)} for all i<n and a surjection \pi ^{n)} _{n(X} →\pi _{n(X)} .

CW approximation

f \colon Z\to X that is called a CW approximation to X. CW approximation, being a weak homotopy equivalence, induces isomorphisms on homology and cohomology groups of X. Thus one often can use CW approximation to reduce a general statement to a simpler version that only concerns CW complexes.Z _{i} of Z , so that the maps (f _{i)} _{*\colon} \pi _{k} (Z _{i)\to} \pi _{k(X)} are isomorphic for k< i and are onto for k = i (for any basepoint). Then Z _{i+1} is built from Z _{i} by attaching (i+1)-cells that (for all basepoints)

• are attached by the mappings

S ^{i} \to Z _{i} that generate the kernel of \pi _{i} (Z _{i)\to} \pi _{i(X)} (and are mapped to X by the contraction of the corresponding spheroids)

• are attached by constant mappings and are mapped to X to generate

\pi _{i+1} (X) (or \pi _{i+1} (X)/(f _{i)} _{*} (\pi _{i+1} (Z _{i))} ).

The cellular approximation ensures then that adding (i+1)-cells doesn't affect

\pi _{k} (Z _{i)\stackrel{\cong}{\to}} \pi _{k} (X) for k<i , while \pi _{i} (Z _{i)} gets factored by the classes of the attachment mappings S ^{i} \to Z _{i} of these cells giving \pi _{i} (Z _{i+1} )\stackrel{\cong}{\to} \pi _{i} (X) . Surjectivity of \pi _{i+1} (Z _{i+1} )\to \pi _{i+1} (X) is evident from the second step of the construction