Abstract.
In
this
study,
we
present
and
analyze
the
first
continuous
timeseries
of
relevant
aerosol
precursor
vapors
from
central
Arctic
during
Multidisciplinary
drifting
Observatory
for
Study
Climate
(MOSAiC)
expedition.
These
include
sulfuric
acid
(SA),
methanesulfonic
(MSA),
iodic
(IA).
We
use
FLEXPART
simulations,
inverse
modeling,
sulfur
dioxide
(SO2)
mixing
ratios,
chlorophyll-a
(chl-a)
observations
to
interpret
20
seasonal
variability
vapor
concentrations
identify
dominant
sources.
Our
results
show
that
both
natural
anthropogenic
sources
are
SA
in
Arctic,
but
associated
with
haze
most
prevalent.
MSA
an
order
magnitude
higher
polar
day
than
night
due
changes
biological
activity.
Peak
were
observed
May,
which
corresponds
timing
annual
peak
chl-a
north
75°
N.
IA
exhibit
two
distinct
peaks
25
year:
a
spring
secondary
autumn,
suggesting
depend
on
solar
radiation
sea
ice
conditions.
general,
cycles
SA,
MSA,
Ocean
related
conditions,
expect
environment
will
affect
these
future.
The
subsequent
influence
processes
remains
uncertain,
highlighting
need
continued
Arctic.
Atmospheric chemistry and physics,
Journal Year:
2023,
Volume and Issue:
23(5), P. 2927 - 2961
Published: March 6, 2023
Abstract.
In
the
Arctic,
aerosol
budget
plays
a
particular
role
in
determining
behaviour
of
clouds,
which
are
important
for
surface
energy
balance
and
thus
region’s
climate.
A
key
question
is
extent
to
cloud
condensation
nuclei
high
Arctic
summertime
boundary
layer
controlled
by
local
emission
formation
processes
as
opposed
transport
from
outside.
Each
these
sources
likely
respond
differently
future
changes
ice
cover.
Here
we
use
global
model
observations
ship
aircraft
field
campaigns
understand
source
late
summer.
We
find
that
particles
formed
remotely,
i.e.
at
latitudes
outside
dominant
Aitken
mode
during
sea
melt
period
up
end
August.
Particles
such
remote
sources,
entrained
into
free
troposphere,
account
nucleation
particle
concentrations
otherwise
underestimated
model.
This
declines
photochemical
rates
decrease
towards
summer
largely
replaced
new
driven
iodic
acid
created
freeze-up.
Such
increases
simulated
2
orders
magnitude
freeze-up
consistent
with
strong
fluctuations
occur
September.
Our
results
suggest
high-Arctic
regime
shift
summer,
only
after
this
do
become
sensitive
processes.
Elementa Science of the Anthropocene,
Journal Year:
2024,
Volume and Issue:
12(1)
Published: Jan. 1, 2024
Low-level
clouds
in
the
Arctic
affect
surface
energy
budget
and
vertical
transport
of
heat
moisture.
The
limited
availability
cloud-droplet-forming
aerosol
particles
strongly
impacts
cloud
properties
lifetime.
Vertical
particle
distributions
are
required
to
study
aerosol–cloud
interaction
over
sea
ice
comprehensively.
This
article
presents
vertically
resolved
measurements
number
concentrations
sizes
using
tethered
balloons.
data
were
collected
during
Multidisciplinary
drifting
Observatory
for
Study
Climate
expedition
summer
2020.
Thirty-four
profiles
concentration
observed
2
size
ranges:
12–150
nm
(N12−150)
above
150
(N>150).
Concurrent
balloon-borne
meteorological
provided
context
continuous
through
cloudy
atmospheric
boundary
layer.
Radiosoundings,
remote
sensing
data,
5-day
back
trajectories
supplemented
analysis.
majority
showed
more
lowest
temperature
inversion,
on
average,
double
compared
below.
Increased
N12−150
up
3,000
cm−3
free
troposphere
low-level
related
secondary
formation.
Long-range
pollution
increased
N>150
310
a
warm,
moist
air
mass.
Droplet
activation
inside
caused
reductions
by
100%,
while
decrease
was
less
than
50%.
When
thermodynamically
coupled
with
surface,
5
times
higher
values
below
cloud-capping
inversion.
Enhanced
interacting
advected
inversion
from
beyond
edge
when
decoupled
surface.
Vertically
discontinuous
suggest
that
emitted
at
not
transported
these
conditions.
It
is
concluded
cloud-surface
coupling
state
tropospheric
abundance
crucial
assessing
ice.
Atmospheric chemistry and physics,
Journal Year:
2024,
Volume and Issue:
24(20), P. 11791 - 11805
Published: Oct. 23, 2024
Abstract.
The
aerosol
particles
serving
as
cloud
condensation
and
ice
nuclei
contribute
to
key
processes
associated
with
cold-air
outbreak
(CAO)
events
but
are
poorly
constrained
in
climate
models
due
sparse
observations.
Here
we
retrieve
number
size
distribution
modes
from
measurements
at
Andenes,
Norway,
during
the
Cold-Air
Outbreaks
Marine
Boundary
Layer
Experiment
(COMBLE)
Zeppelin
Observatory,
approximately
1000
km
upwind
Andenes
Svalbard.
During
CAO
sea-spray-mode
concentration
is
correlated
strong
over-ocean
winds
a
mean
of
8±4
cm−3
that
71
%
higher
than
non-CAO
conditions.
Additionally,
Hoppel
minimum
diameter
6
nm
smaller
conditions,
though
estimated
supersaturation
lower,
likely
activated
in-cloud
109±61
no
statistically
significant
difference
99±66
cm−3.
For
trajectories
between
Observatory
upwind-to-downwind
change
largest
for
accumulation
mode
decrease
93±95
cm−3,
attributable
primarily
precipitation
scavenging.
These
characteristic
properties
distributions
provide
guidance
evaluating
aerosol–cloud
interaction
models.
Atmospheric chemistry and physics,
Journal Year:
2024,
Volume and Issue:
24(22), P. 12595 - 12621
Published: Nov. 14, 2024
Abstract.
In
this
study,
we
present
and
analyze
the
first
continuous
time
series
of
relevant
aerosol
precursor
vapors
from
central
Arctic
(north
80°
N)
during
Multidisciplinary
drifting
Observatory
for
Study
Climate
(MOSAiC)
expedition.
These
include
sulfuric
acid
(SA),
methanesulfonic
(MSA),
iodic
(IA).
We
use
FLEXPART
simulations,
inverse
modeling,
sulfur
dioxide
(SO2)
mixing
ratios,
chlorophyll
a
(chl
a)
observations
to
interpret
seasonal
variability
in
vapor
concentrations
identify
dominant
sources.
Our
results
show
that
both
natural
anthropogenic
sources
are
SA
Arctic,
but
associated
with
haze
most
prevalent.
MSA
an
order
magnitude
higher
polar
day
than
night
due
changes
biological
activity.
Peak
were
observed
May,
which
corresponds
timing
annual
peak
chl
north
75°
N.
IA
exhibit
two
distinct
peaks
year,
namely
spring
secondary
autumn,
suggesting
depend
on
solar
radiation
sea
ice
conditions.
general,
cycles
SA,
MSA,
Ocean
related
conditions,
expect
environment
will
affect
these
future.
The
subsequent
influence
processes
remains
uncertain,
highlighting
need
continued
Arctic.
Abstract.
The
role
aerosol
chemical
composition
plays
in
Arctic
low-level
cloud
formation
is
still
poorly
understood.
In
this
study
we
address
issue
by
combining
situ
observations
of
the
characteristics
residuals
(dried
liquid
droplets
or
ice
crystals)
and
particles
from
Zeppelin
Observatory
Ny-Ålesund,
Svalbard
(approx.
480
m
a.
s.
l.).
These
measurements
were
part
one-year
long
Ny-Ålesund
Aerosol
Cloud
Experiment
2019–2020
(NASCENT).
To
obtain
at
molecular
level,
deployed
a
Filter
Inlet
for
Gases
AEROsols
coupled
to
Chemical
Ionization
Mass
Spectrometer
(FIGAERO-CIMS)
with
iodide
as
reagent
ion
behind
Ground-based
Counterflow
Virtual
Impactor
(GCVI).
station
was
enshrouded
clouds
roughly
15
%
time
during
NASCENT,
out
which
analyzed
14
events
between
December
2019
2020.
During
entire
year,
shows
contributions
oxygenated
organic
compounds,
including
organonitrates,
traces
biomass
burning
tracer
levoglucosan.
summer,
methanesulfonic
acid
(MSA),
an
oxidation
product
dimethyl
sulfide
(DMS),
large
sampled
mass,
indicating
marine
natural
sources
condensation
nuclei
(CCN)
nucleating
(INP)
mass
sunlit
year.
addition,
also
find
inorganic
acids
nitric
sulfuric
acid,
outstanding
high
absolute
signals
one
residual
sample
spring
late
summer
(May
21
September
12,
2020),
probably
caused
anthropogenic
sulfur
emissions
near
Barents
Kara
Sea.
particular
event,
on
May
18,
2020,
air
origin
did
not
change
before
after
cloud.
We
therefore
chose
it
case
investigate
impact
physicochemical
properties.
show
that
overall
similar
before,
during,
cloud,
have
already
undergone
several
cycles
processing
being
measured
Zeppelin,
and/or
timescales
observed
fraction
can
be
neglected.
Meanwhile
there
are
average
fewer
particles,
but
relatively
more
accumulation
mode
Comparing
signal
sulfur-containing
compounds
aerosols
cloud-free
conditions,
has
higher
relative
contribution
compared
observe
increase
particulate
MSA
due
Overall,
composition,
especially
residuals,
reflects
general
population
well.
Our
results
thus
suggest
most
serve
seeds
Arctic.
Atmospheric chemistry and physics,
Journal Year:
2023,
Volume and Issue:
23(12), P. 7033 - 7055
Published: June 26, 2023
Abstract.
Climate
change
is
particularly
noticeable
in
the
Arctic.
The
most
common
type
of
cloud
at
these
latitudes
mixed-phase
stratocumulus.
These
clouds
occur
frequently
and
persistently
during
all
seasons
play
a
critical
role
Arctic
energy
budget.
Previous
observations
central
(north
80∘
N)
have
shown
high
occurrence
prolonged
periods
shallow,
single-layer
stratocumulus
top
boundary
layer
(BL;
altitudes
∼
300
to
400
m).
However,
recent
from
summer
2018
instead
showed
prevalence
two-layer
boundary-layer
system.
Here
we
use
large-eddy
simulation
examine
maintenance
one
systems
observed
sensitivity
layers
different
micro-
macro-scale
parameters.
We
find
that
model
generally
reproduces
thermodynamic
structure
well,
with
two
near-neutrally
stratified
BL
caused
by
low
(located
within
first
few
hundred
meters)
capped
lower-altitude
temperature
inversion
an
upper
(based
around
kilometer
or
slightly
higher)
main
BL.
simulated
persistent
unless
there
are
aerosol
number
concentrations
(≤
5
cm−3),
which
cause
dissipate,
large-scale
wind
speeds
(≥
8.5
m
s−1),
erode
lower
related
layer.
changes
alter
both
short-
longwave
radiative
effect
surface.
This
results
net
modeled
system,
can
impact
surface
melting
freezing.
findings
highlight
importance
better
understanding
representing
sources
sinks
over
Ocean.
Furthermore,
they
underline
significance
meteorological
parameters,
such
as
speed,
for
maintaining
encountered
atmosphere
Abstract.
Mixed-phase
clouds
(MPC)
are
key
players
in
the
Arctic
climate
system
due
to
their
role
modulating
solar
and
terrestrial
radiation.
Such
radiative
interactions
critically
rely
on
ice
content
of
MPC
which,
turn,
also
depend
availability
nucleating
particles
(INP).
INP
sources
concentrations
poorly
understood
Arctic.
Recently,
active
at
high
temperatures
were
associated
with
presence
primary
biological
aerosol
(PBAP).
Here,
we
investigated
for
a
full
year
abundance
variability
fluorescent
PBAP
(fPBAP)
within
cloud
residuals,
directly
sampled
by
multiparameter
bioaerosol
spectrometer
coupled
ground-based
counterflow
virtual
impactor
inlet
Zeppelin
Observatory
(475
m
asl),
Ny-Ålesund,
Svalbard.
fPBAP
(10-3–10-2
L-1)
contributions
coarse-mode
(0.1
1
every
103
particles)
residuals
found
be
close
those
expected
high-temperature
INP.
Transmission
electron
microscopy
confirmed
fPBAP,
most
likely
bacteria,
residual
samples.
Seasonally,
our
results
reveal
an
elevated
summer.
Parallel
water
vapor
isotope
measurements
point
towards
link
between
summer
regionally
sourced
air
masses.
Low-level
predominantly
observed
beginning
end
summer,
one
explanation
is
existence
In
this
study,
present
observational
evidence
that
may
play
important
determining
phase
low-level
clouds.
These
findings
have
potential
implications
future
description
condensation
nuclei
given
ongoing
changes
hydrological
biogeochemical
cycles
will
influence
flux
Abstract.
In
this
study,
we
present
and
analyze
the
first
continuous
timeseries
of
relevant
aerosol
precursor
vapors
from
central
Arctic
during
Multidisciplinary
drifting
Observatory
for
Study
Climate
(MOSAiC)
expedition.
These
include
sulfuric
acid
(SA),
methanesulfonic
(MSA),
iodic
(IA).
We
use
FLEXPART
simulations,
inverse
modeling,
sulfur
dioxide
(SO2)
mixing
ratios,
chlorophyll-a
(chl-a)
observations
to
interpret
20
seasonal
variability
vapor
concentrations
identify
dominant
sources.
Our
results
show
that
both
natural
anthropogenic
sources
are
SA
in
Arctic,
but
associated
with
haze
most
prevalent.
MSA
an
order
magnitude
higher
polar
day
than
night
due
changes
biological
activity.
Peak
were
observed
May,
which
corresponds
timing
annual
peak
chl-a
north
75°
N.
IA
exhibit
two
distinct
peaks
25
year:
a
spring
secondary
autumn,
suggesting
depend
on
solar
radiation
sea
ice
conditions.
general,
cycles
SA,
MSA,
Ocean
related
conditions,
expect
environment
will
affect
these
future.
The
subsequent
influence
processes
remains
uncertain,
highlighting
need
continued
Arctic.
Abstract.
Mixed-phase
clouds
(MPC)
are
key
players
in
the
Arctic
climate
system
due
to
their
role
modulating
solar
and
terrestrial
radiation.
Such
radiative
interactions
critically
rely
on
ice
content
of
MPC
which,
turn,
also
depend
availability
nucleating
particles
(INP).
INP
sources
concentrations
poorly
understood
Arctic.
Recently,
active
at
high
temperatures
were
associated
with
presence
primary
biological
aerosol
(PBAP).
Here,
we
investigated
for
a
full
year
abundance
variability
fluorescent
PBAP
(fPBAP)
within
cloud
residuals,
directly
sampled
by
multiparameter
bioaerosol
spectrometer
coupled
ground-based
counterflow
virtual
impactor
inlet
Zeppelin
Observatory
(475
m
asl),
Ny-Ålesund,
Svalbard.
fPBAP
(10-3–10-2
L-1)
contributions
coarse-mode
(0.1
1
every
103
particles)
residuals
found
be
close
those
expected
high-temperature
INP.
Transmission
electron
microscopy
confirmed
fPBAP,
most
likely
bacteria,
residual
samples.
Seasonally,
our
results
reveal
an
elevated
summer.
Parallel
water
vapor
isotope
measurements
point
towards
link
between
summer
regionally
sourced
air
masses.
Low-level
predominantly
observed
beginning
end
summer,
one
explanation
is
existence
In
this
study,
present
observational
evidence
that
may
play
important
determining
phase
low-level
clouds.
These
findings
have
potential
implications
future
description
condensation
nuclei
given
ongoing
changes
hydrological
biogeochemical
cycles
will
influence
flux