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dm: ensure bio submission follows a depth-first tree walk
A dm device can, in general, represent a tree of targets, each of which handles a sub-range of the range of blocks handled by the parent. The bio sequencing managed by generic_make_request() requires that bios are generated and handled in a depth-first manner. Each call to a make_request_fn() may submit bios to a single member device, and may submit bios for a reduced region of the same device as the make_request_fn. In particular, any bios submitted to member devices must be expected to be processed in order, so a later one must never wait for an earlier one. This ordering is usually achieved by using bio_split() to reduce a bio to a size that can be completely handled by one target, and resubmitting the remainder to the originating device. bio_queue_split() shows the canonical approach. dm doesn't follow this approach, largely because it has needed to split bios since long before bio_split() was available. It currently can submit bios to separate targets within the one dm_make_request() call. Dependencies between these targets, as can happen with dm-snap, can cause deadlocks if either bios gets stuck behind the other in the queues managed by generic_make_request(). This requires the 'rescue' functionality provided by dm_offload_{start,end}. Some of this requirement can be removed by changing the order of bio submission to follow the canonical approach. That is, if dm finds that it needs to split a bio, the remainder should be sent to generic_make_request() rather than being handled immediately. This delays the handling until the first part is completely processed, so the deadlock problems do not occur. __split_and_process_bio() can be called both from dm_make_request() and from dm_wq_work(). When called from dm_wq_work() the current approach is perfectly satisfactory as each bio will be processed immediately. When called from dm_make_request(), current->bio_list will be non-NULL, and in this case it is best to create a separate "clone" bio for the remainder. When we use bio_clone_bioset() to split off the front part of a bio and chain the two together and submit the remainder to generic_make_request(), it is important that the newly allocated bio is used as the head to be processed immediately, and the original bio gets "bio_advance()"d and sent to generic_make_request() as the remainder. Otherwise, if the newly allocated bio is used as the remainder, and if it then needs to be split again, then the next bio_clone_bioset() call will be made while holding a reference a bio (result of the first clone) from the same bioset. This can potentially exhaust the bioset mempool and result in a memory allocation deadlock. Note that there is no race caused by reassigning cio.io->bio after already calling __map_bio(). This bio will only be dereferenced again after dec_pending() has found io->io_count to be zero, and this cannot happen before the dec_pending() call at the end of __split_and_process_bio(). To provide the clone bio when splitting, we use q->bio_split. This was previously being freed by bio-based dm to avoid having excess rescuer threads. As bio_split bio sets no longer create rescuer threads, there is little cost and much gain from restoring the q->bio_split bio set. Signed-off-by: NeilBrown <neilb@suse.com> Signed-off-by: Mike Snitzer <snitzer@redhat.com>
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@ -1498,8 +1498,29 @@ static void __split_and_process_bio(struct mapped_device *md,
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} else {
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} else {
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ci.bio = bio;
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ci.bio = bio;
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ci.sector_count = bio_sectors(bio);
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ci.sector_count = bio_sectors(bio);
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while (ci.sector_count && !error)
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while (ci.sector_count && !error) {
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error = __split_and_process_non_flush(&ci);
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error = __split_and_process_non_flush(&ci);
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if (current->bio_list && ci.sector_count && !error) {
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/*
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* Remainder must be passed to generic_make_request()
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* so that it gets handled *after* bios already submitted
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* have been completely processed.
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* We take a clone of the original to store in
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* ci.io->bio to be used by end_io_acct() and
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* for dec_pending to use for completion handling.
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* As this path is not used for REQ_OP_ZONE_REPORT,
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* the usage of io->bio in dm_remap_zone_report()
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* won't be affected by this reassignment.
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*/
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struct bio *b = bio_clone_bioset(bio, GFP_NOIO,
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md->queue->bio_split);
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ci.io->bio = b;
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bio_advance(bio, (bio_sectors(bio) - ci.sector_count) << 9);
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bio_chain(b, bio);
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generic_make_request(bio);
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break;
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}
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}
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}
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}
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/* drop the extra reference count */
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/* drop the extra reference count */
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@ -1510,8 +1531,8 @@ static void __split_and_process_bio(struct mapped_device *md,
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*---------------------------------------------------------------*/
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*---------------------------------------------------------------*/
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/*
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/*
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* The request function that just remaps the bio built up by
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* The request function that remaps the bio to one target and
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* dm_merge_bvec.
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* splits off any remainder.
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*/
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*/
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static blk_qc_t dm_make_request(struct request_queue *q, struct bio *bio)
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static blk_qc_t dm_make_request(struct request_queue *q, struct bio *bio)
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{
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{
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@ -2034,12 +2055,6 @@ int dm_setup_md_queue(struct mapped_device *md, struct dm_table *t)
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case DM_TYPE_DAX_BIO_BASED:
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case DM_TYPE_DAX_BIO_BASED:
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dm_init_normal_md_queue(md);
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dm_init_normal_md_queue(md);
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blk_queue_make_request(md->queue, dm_make_request);
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blk_queue_make_request(md->queue, dm_make_request);
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/*
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* DM handles splitting bios as needed. Free the bio_split bioset
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* since it won't be used (saves 1 process per bio-based DM device).
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*/
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bioset_free(md->queue->bio_split);
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md->queue->bio_split = NULL;
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if (type == DM_TYPE_DAX_BIO_BASED)
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if (type == DM_TYPE_DAX_BIO_BASED)
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queue_flag_set_unlocked(QUEUE_FLAG_DAX, md->queue);
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queue_flag_set_unlocked(QUEUE_FLAG_DAX, md->queue);
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