Authorea (Authorea),
Journal Year:
2023,
Volume and Issue:
unknown
Published: Feb. 20, 2023
Trends
in
tropospheric
ozone,
an
important
air
pollutant
and
short-lived
climate
forcer
(SLCF),
are
estimated
using
available
surface
ozonesonde
profile
data
for
1993-2019.
Using
a
coherent
methodology,
observed
trends
compared
to
modeled
(1995-2015)
from
the
Arctic
Monitoring
Assessment
Programme
SLCF
2021
assessment.
Statistically
significant
increases
ozone
at
coastal
sites,
notably
during
winter,
concurrent
decreasing
carbon
monoxide,
generally
captured
by
multi-model
median
(MMM)
trends.
Wintertime
also
free
troposphere
most
but
tend
be
overestimated
MMMs.
Springtime
northern
Alaska
not
simulated
while
negative
springtime
Scandinavia
always
reproduced.
Possible
reasons
changes
model
behavior
discussed,
including
precursor
emissions,
changing
sinks,
variability
large-scale
meteorology.
Abstract
The
atmospheric
methane
trend
is
not
fully
understood.
Here
we
investigate
the
role
of
main
sink,
natural
source,
and
anthropogenic
emissions
on
growth
rate
over
last
three
decades
using
numerical
models
emission
inventories.
We
find
that
long-term
driven
by
increased
emissions,
while
wetland
show
large
variability
can
modify
trend.
influence
hydroxyl
radical,
through
nitrogen
oxides
carbon
monoxide
has
modified
contributed
to
stabilization
from
2000
2007.
radical
increase
prior
this
period
might
have
decline
in
isotopic
ratio
after
2007
due
time
dependent
response
radical.
Emission
reductions
COVID-19
restrictions
via
possibly
approximately
two
thirds
2019
2020.
Journal of Geophysical Research Atmospheres,
Journal Year:
2022,
Volume and Issue:
127(11)
Published: May 25, 2022
Detailed
knowledge
of
the
physical
and
chemical
properties
sources
particles
that
form
clouds
is
especially
important
in
pristine
areas
like
Arctic,
where
particle
concentrations
are
often
low
observations
sparse.
Here,
we
present
situ
cloud
aerosol
measurements
from
central
Arctic
Ocean
August-September
2018
combined
with
air
parcel
source
analysis.
We
provide
direct
experimental
evidence
Aitken
mode
(particles
diameters
≲70
nm)
significantly
contribute
to
condensation
nuclei
(CCN)
or
droplet
residuals,
after
freeze-up
sea
ice
transition
toward
fall.
These
were
associated
spent
more
time
over
pack
ice,
while
size
distributions
dominated
by
accumulation
≳70
showed
a
stronger
contribution
oceanic
slightly
different
regions.
This
was
accompanied
changes
average
composition
an
increased
relative
organic
material
Addition
mass
due
aqueous-phase
chemistry
during
in-cloud
processing
probably
small
given
fact
observed
very
similar
both
whole-air
residual
data.
aerosol-cloud
interaction
valuable
insight
into
origin
CCN
Ocean.
Atmospheric chemistry and physics,
Journal Year:
2025,
Volume and Issue:
25(1), P. 143 - 156
Published: Jan. 8, 2025
Abstract.
Forest
wildfires
in
interior
Alaska
represent
an
important
black
carbon
(BC)
source
for
the
Arctic
and
sub-Arctic.
However,
BC
observations
have
not
been
sufficient
to
constrain
range
of
existing
emissions.
Here,
we
show
our
mass
concentrations
monoxide
(CO)
mixing
ratios
Poker
Flat
Research
Range
(65.12°
N,
147.43°
W),
located
central
Alaska,
from
April
2016
December
2020.
The
medians,
10th
percentile
ranges,
90th
ranges
hourly
concentration
CO
ratio
throughout
observation
period
were
13,
2.9,
56
ng
m−3
124.7,
98.7,
148.3
ppb,
respectively.
Sporadically
large
peaks
observed
at
same
time,
indicating
influences
common
sources.
These
coincided
with
other
comparative
sites
emissions
Alaska.
Source
estimation
by
FLEXPART-WRF
(Flexible
Particle
Dispersion–Weather
Forecast)
confirmed
a
contribution
boreal
forest
western
Canada
when
high
observed.
For
these
cases,
found
positive
correlation
(r=0.44)
between
BC/ΔCO
fire
radiative
power
(FRP)
Canada.
This
finding
implies
that
variability
emission
is
associated
intensity
time
progress
suggests
factor
and/or
inventory
could
be
potentially
improved
FRP.
We
recommend
FRP
integrated
into
future
bottom-up
inventories
achieve
better
understanding
dynamics
pollutants
frequently
occurring
under
rapidly
changing
climate
Arctic.
Abstract
A
key
driving
factor
behind
rapid
Arctic
climate
change
is
black
carbon,
the
atmospheric
aerosol
that
most
efficiently
absorbs
sunlight.
Our
knowledge
about
carbon
in
scarce,
mainly
limited
to
long-term
measurements
of
a
few
ground
stations
and
snap-shots
by
aircraft
observations.
Here,
we
combine
observations
from
campaigns
performed
over
nine
years,
present
vertically
resolved
average
properties.
four
higher
mass
concentration
(21.6
ng
m
−3
average,
14.3
median)
was
found
spring,
compared
summer
(4.7
3.9
median).
In
much
inter-annual
geographic
variability
prevailed
stable
situation
summer.
The
shape
size
distributions
remained
constant
between
seasons
with
an
mean
diameter
202
nm
spring
210
Comparison
concentrations
simulated
global
model
shows
notable
discrepancies,
highlighting
need
for
further
developments
intensified
measurements.
Atmospheric chemistry and physics,
Journal Year:
2023,
Volume and Issue:
23(1), P. 637 - 661
Published: Jan. 16, 2023
Abstract.
As
the
third
most
important
greenhouse
gas
(GHG)
after
carbon
dioxide
(CO2)
and
methane
(CH4),
tropospheric
ozone
(O3)
is
also
an
air
pollutant
causing
damage
to
human
health
ecosystems.
This
study
brings
together
recent
research
on
observations
modeling
of
O3
in
Arctic,
a
rapidly
warming
sensitive
environment.
At
different
locations
observed
surface
seasonal
cycles
are
quite
different.
Coastal
Arctic
locations,
for
example,
have
minimum
springtime
due
depletion
events
resulting
from
bromine
chemistry.
In
contrast,
other
maximum
spring.
The
12
state-of-the-art
models
used
this
lack
halogen
chemistry
needed
simulate
coastal
springtime;
however,
multi-model
median
(MMM)
has
accurate
at
non-coastal
locations.
There
large
amount
variability
among
models,
which
been
previously
reported,
we
show
that
there
continues
be
no
convergence
or
improved
accuracy
simulating
its
precursor
species.
MMM
underestimates
by
5
%
15
depending
location.
vertical
distribution
studied
ozonesonde
measurements
models.
highly
variable,
free-tropospheric
within
range
±50
model
altitude.
performs
best,
±8
seasons.
However,
nearly
all
overestimate
near
tropopause
(∼300
hPa
∼8
km),
likely
ongoing
issues
with
underestimating
altitude
excessive
downward
transport
stratospheric
high
latitudes.
For
biased
about
20
Eureka.
Observed
simulated
precursors
(CO,
NOx,
reservoir
PAN)
evaluated
throughout
troposphere.
Models
underestimate
wintertime
CO
everywhere,
combination
emissions
possibly
overestimating
OH.
Throughout
profile
(compared
aircraft
measurements),
both
NOx
but
overestimates
PAN.
Perhaps
as
result
competing
deficiencies,
matches
reasonably
well.
Our
findings
suggest
despite
updates
over
last
decade,
results
variable
ever
not
increased
representing
O3.
Atmosphere,
Journal Year:
2023,
Volume and Issue:
14(1), P. 139 - 139
Published: Jan. 8, 2023
The
results
of
the
research
are
numerical
estimates
average
fields
black
carbon
mass
concentration
in
surface
layer
atmosphere
Arctic
region
obtained
using
numeric
technology
referred
to
as
fluid
location
(FLA).
modelling
has
been
based
on
measurements
concentrations
near-surface
during
two
cruises
Professor
Multanovskiy
(28
July–7
September
2019)
and
Akademik
Mstislav
Keldysh
(31
July–24
August
2020)
vessels.
These
have
supplemented
by
at
stationary
monitoring
points
located
Spitsbergen
Severnaya
Zemlya
archipelagoes.
simulation
summertime
demonstrates
that
areas
increased
were
observed
over
Northern
Europe
and,
2019,
also
Laptev
Sea
basin.
spatial
distribution
qualitatively
agreed
with
same
data
derived
from
second
Modern-Era
Retrospective
analysis
for
Research
Applications
(MERRA-2)
but
showed
quantitative
differences.
values
zones
follows:
85.3
ng/m3
(2019)
53.6
(2020)
reconstructed
FLA
technology;
261.69
131.8
MERRA-2
data.
Geophysical Research Letters,
Journal Year:
2023,
Volume and Issue:
50(22)
Published: Nov. 20, 2023
Abstract
Observed
trends
in
tropospheric
ozone,
an
important
air
pollutant
and
short‐lived
climate
forcer
(SLCF),
are
estimated
using
available
surface
ozonesonde
profile
data
for
1993–2019,
a
coherent
methodology,
compared
to
modeled
(1995–2015)
from
the
Arctic
Monitoring
Assessment
Program
SLCF
2021
assessment.
Increases
observed
ozone
at
coastal
sites,
notably
during
winter,
concurrent
decreasing
carbon
monoxide,
generally
captured
by
multi‐model
median
trends.
Wintertime
increases
also
free
troposphere
most
with
decreases
spring
months.
Winter
tend
be
overestimated
medians.
Springtime
northern
Alaska
not
simulated
while
negative
springtime
Scandinavia
always
reproduced.
Possible
reasons
changes
model
performance
discussed
including
precursor
emissions,
changing
dry
deposition,
variability
large‐scale
meteorology.
Journal of Geophysical Research Atmospheres,
Journal Year:
2025,
Volume and Issue:
130(7)
Published: April 8, 2025
Abstract
Air
pollutants
are
primarily
transported
from
midlatitude
emission
regions
in
winter
and
early
spring,
leading
to
elevated
concentrations
of
aerosols,
including
black
carbon
(BC),
the
Arctic,
a
phenomenon
known
as
Arctic
haze.
The
Weather
Research
Forecasting
model
coupled
with
chemistry
is
used
investigate
potential
causes
uncertainties
modeling
BC
for
2014.
captures
observed
variability
at
surface
sites,
reproducing
Zeppelin
but
showing
low
bias
Tiksi,
Alert,
Utqiaġvik/Barrow.
influence
removal
processes
on
biases
explored
by
switching
off
dry
or
wet
deposition.
Wet
deposition,
during
transport
North
Atlantic
storm
track,
locally
over
Svalbard,
dominates
Zeppelin,
while
Pacific
track
influences
Alert
Dry
Asian
source
Alaska
affects
Utqiaġvik/Barrow,
larger
than
Tiksi
due
proximity
local/regional
anthropogenic
sources.
Regional
runs
northern
late
January
show
improved
simulated
compared
observations
part,
better
resolution
processes,
emissions.
Sensitivity
also
that
regional
Alaskan
sources,
notably
Slope
oil
fields,
may
be
contributing
30%–50%,
average,
Utqiaġvik/Barrow
February
2014,
remainder
outside
region.
These
findings
highlight
importance
local
emissions,
need
inventories
Arctic.
Atmospheric chemistry and physics,
Journal Year:
2023,
Volume and Issue:
23(14), P. 7955 - 7973
Published: July 18, 2023
Abstract.
Aerosol–cloud
interaction
is
considered
one
of
the
largest
sources
uncertainty
in
radiative
forcing
estimations.
To
better
understand
role
black
carbon
(BC)
aerosol
as
a
cloud
nucleus
and
impact
clouds
on
its
vertical
distribution
Arctic,
we
report
airborne
situ
measurements
BC
particles
European
Arctic
near
Svalbard
during
“Arctic
CLoud
Observations
Using
polar
Day”
(ACLOUD)
campaign
held
summer
2017.
was
measured
with
single-particle
soot
photometer
aboard
Polar
6
research
aircraft
from
lowest
atmospheric
layer
up
to
approximately
3500
m
a.s.l
(metres
above
sea
level).
During
in-cloud
flight
transects,
contained
liquid
droplets
(BC
residuals)
were
sampled
through
counterflow
virtual
impactor
(CVI)
inlet.
Four
flights,
conducted
presence
low-level,
surface-coupled,
inside-inversion,
mixed-phase
over
ice,
selected
address
variability
above,
below,
within
layer.
First,
increase
size
coating
thickness
free
troposphere
cloud-dominated
boundary
confirmed
that
ground
observations
not
representative
upper
layers.
Second,
although
only
1
%
particle,
higher
number
concentration
residuals
than
below
indicated
totality
below-cloud
activated
by
nucleation
scavenging
but
also
alternative
processes
such
activation
free-tropospheric
at
top
might
occur.
Third,
efficient
exchange
bottom
similarity
cloud.
Last,
residual
(+31
%)
geometric
mean
diameter
(+38
absolute
enrichment
larger
compared
outside
supported
hypothesis
concomitant
mechanisms
suggested
formation
agglomerates
caused
processing.
The
evolution
properties
inside
an
bottom,
which
include
activation,
processing,
sub-cloud
release
processed
agglomerates.
In
case
persistent
low-level
clouds,
this
cycle
may
reiterate
multiple
times,
adding
additional
degree
complexity
understanding
processing
Arctic.