On Wed, Sep 25, 2013 at 02:17:02PM -0700, Zach Brown wrote:
> > void zero_fill_bio(struct bio *bio)
> > {
> > - unsigned long flags;
> > struct bio_vec bv;
> > struct bvec_iter iter;
> >
> > - bio_for_each_segment(bv, bio, iter) {
> > +#if defined(CONFIG_HIGHMEM) || defined(ARCH_IMPLEMENTS_FLUSH_DCACHE_PAGE)
> > + bio_for_each_page(bv, bio, iter) {
> > + unsigned long flags;
> > char *data = bvec_kmap_irq(&bv, &flags);
> > memset(data, 0, bv.bv_len);
> > flush_dcache_page(bv.bv_page);
> > bvec_kunmap_irq(data, &flags);
> > }
> > +#else
> > + bio_for_each_segment(bv, bio, iter)
> > + memset(page_address(bv.bv_page) + bv.bv_offset,
> > + 0, bv.bv_len);
> > +#endif
>
> This looks pretty sketchy. I'd expect this to be doable with one loop
> and that bvec_kmap_irq() and flush_dcache_page() would fall back to
> page_address() and nops when they're not needed.
>
> Where did this come from?
It's just that if we need the kmap or the flush_dcache_page we have to
process the bio one 4k page at a time - if not, we can process 64k (or
whatever) bvecs all at once. That doesn't just save us memcpy calls, we
can also avoid all the machinery in bio_for_each_page() for chunking up
large bvecs into single page bvecs.
I can definitely think of better ways to do this, but I figured I'd wait
and see if other code ends up wanting to switch between
bio_for_each_page() and bio_for_each_segment() and why.
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