Secondary
organic
aerosol
(SOA)
exerts
a
considerable
influence
on
atmospheric
chemistry.
However,
little
information
about
the
vertical
distribution
of
SOA
in
alpine
setting
is
available,
which
limited
simulation
using
chemical
transport
models.
Here,
total
15
biogenic
and
anthropogenic
tracers
were
measured
PM2.5
aerosols
at
both
summit
(1840
m
a.s.l.)
foot
(480
Mt.
Huang
during
winter
2020
to
explore
their
formation
mechanism.
Most
determined
species
(e.g.,
BSOA
ASOA
tracers,
carbonaceous
components,
major
inorganic
ions)
gaseous
pollutants
presented
higher
concentrations
than
those
summit,
suggesting
relatively
more
significant
effect
emissions
ground
level.
The
ISORROPIA-II
model
showed
that
acidity
increases
as
altitude
decreases.
Air
mass
trajectories,
potential
source
contribution
function
(PSCF),
correlation
analysis
with
temperature
revealed
was
mostly
derived
from
local
oxidation
volatile
compounds
(VOCs),
while
mainly
influenced
by
long-distance
transport.
robust
correlations
NH3,
NO2,
SO2)
indicated
could
promote
productions
mountainous
background
atmosphere.
Moreover,
most
correlated
well
levoglucosan
all
samples,
biomass
burning
played
an
important
role
mountain
troposphere.
This
work
demonstrated
daytime
significantly
valley
breeze
winter.
Our
results
provide
new
insights
into
distributions
provenance
free
troposphere
over
East
China.
Abstract.
Nitrogen-containing
organic
compounds
(NOCs)
are
abundant
and
important
aerosol
components,
deeply
involving
in
global
nitrogen
cycle.
However,
the
sources
formation
processes
of
NOCs
remain
largely
unknown,
particularly
city
(Urumqi,
China)
farthest
from
ocean
worldwide.
Here,
PM2.5
collected
Urumqi
over
a
one-year
period
were
characterized
by
ultrahigh-resolution
mass
spectrometry.
The
abundance
CHON
(mainly
poor-O
unsaturated
aliphatic-like
species)
positive
ion
mode
was
higher
warm
than
cold
period,
which
attributed
to
contribution
fresh
biomass
material
combustion
(e.g.,
forest
fires)
associated
with
amidation
fatty
acids
rather
oxidation
processes.
nitro-aromatic
negative
increased
significantly
tightly
related
old-age
dry
straws)
wintertime
Urumqi.
For
CHN
compounds,
we
found
that
alkyl
nitriles
aromatic
CNH
showed
periods,
respectively.
It
further
confirmed
different
impacts
fresh-
materials
on
NOC
compositions.
Our
results
clarify
mechanisms
emitted
NOCs.
Abstract.
Nitrogen-containing
organic
compounds
(NOCs)
are
abundant
and
important
aerosol
components,
deeply
involving
in
global
nitrogen
cycle.
However,
the
sources
formation
processes
of
NOCs
remain
largely
unknown,
particularly
city
(Urumqi,
China)
farthest
from
ocean
worldwide.
Here,
PM2.5
collected
Urumqi
over
a
one-year
period
were
characterized
by
ultrahigh-resolution
mass
spectrometry.
The
abundance
CHON
(mainly
poor-O
unsaturated
aliphatic-like
species)
positive
ion
mode
was
higher
warm
than
cold
period,
which
attributed
to
contribution
fresh
biomass
material
combustion
(e.g.,
forest
fires)
associated
with
amidation
fatty
acids
rather
oxidation
processes.
nitro-aromatic
negative
increased
significantly
tightly
related
old-age
dry
straws)
wintertime
Urumqi.
For
CHN
compounds,
we
found
that
alkyl
nitriles
aromatic
CNH
showed
periods,
respectively.
It
further
confirmed
different
impacts
fresh-
materials
on
NOC
compositions.
Our
results
clarify
mechanisms
emitted
NOCs.
Secondary
organic
aerosol
(SOA)
exerts
a
considerable
influence
on
atmospheric
chemistry.
However,
little
information
about
the
vertical
distribution
of
SOA
in
alpine
setting
is
available,
which
limited
simulation
using
chemical
transport
models.
Here,
total
15
biogenic
and
anthropogenic
tracers
were
measured
PM2.5
aerosols
at
both
summit
(1840
m
a.s.l.)
foot
(480
Mt.
Huang
during
winter
2020
to
explore
their
formation
mechanism.
Most
determined
species
(e.g.,
BSOA
ASOA
tracers,
carbonaceous
components,
major
inorganic
ions)
gaseous
pollutants
presented
higher
concentrations
than
those
summit,
suggesting
relatively
more
significant
effect
emissions
ground
level.
The
ISORROPIA-II
model
showed
that
acidity
increases
as
altitude
decreases.
Air
mass
trajectories,
potential
source
contribution
function
(PSCF),
correlation
analysis
with
temperature
revealed
was
mostly
derived
from
local
oxidation
volatile
compounds
(VOCs),
while
mainly
influenced
by
long-distance
transport.
robust
correlations
NH3,
NO2,
SO2)
indicated
could
promote
productions
mountainous
background
atmosphere.
Moreover,
most
correlated
well
levoglucosan
all
samples,
biomass
burning
played
an
important
role
mountain
troposphere.
This
work
demonstrated
daytime
significantly
valley
breeze
winter.
Our
results
provide
new
insights
into
distributions
provenance
free
troposphere
over
East
China.