Linux kernel for uConsole
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18a25da843
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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Linux kernel ============ This file was moved to Documentation/admin-guide/README.rst Please notice that there are several guides for kernel developers and users. These guides can be rendered in a number of formats, like HTML and PDF. In order to build the documentation, use ``make htmldocs`` or ``make pdfdocs``. There are various text files in the Documentation/ subdirectory, several of them using the Restructured Text markup notation. See Documentation/00-INDEX for a list of what is contained in each file. Please read the Documentation/process/changes.rst file, as it contains the requirements for building and running the kernel, and information about the problems which may result by upgrading your kernel.