The
Third
U.S.
National
Marine
Environmental
DNA
Workshop
on
June
2–5,
2024
brought
together
researchers,
practitioners,
and
policymakers
to
overview
discuss:
(1)
environmental
(e)DNA
–
defined
as
“DNA
in
the
environment”
a
strategic
national
priority,
(2)
eDNA
tool
readiness
approaches
support
decision-making,
(3)
emerging
technologies,
(4)
plans
for
implementation
adoption
monitoring
ecosystem
assessment
“from
microbes
through
whales”.
Uses
applications
of
have
been
revolutionizing
exploration,
measurement,
biodiversity
across
ecosystems,
including
marine
freshwater
aquatic
environments
emphasized
Workshop,
well
terrestrial
aerial
systems.
featured
launch
new
Aquatic
Strategy
from
White
House
Office
Science
Technology
Policy
(2024),
with
ocean
waters,
all
salinities;
was
developed
using
outputs
taskforce
2022
Second
Workshop.
2.5-day
included
speaker
presentations,
panel
discussions,
networking
tools,
applications,
use,
upscaling,
their
future.
led
into
Capitol
Hill
Ocean
Week
(CHOW)
events
(June
5–6,
2024),
during
World
Week.
Note
that
this
summary
paper
represents
author’s
take-away
view
interpretation,
not
necessarily
overall
views
or
consensus
Government,
Smithsonian
Institution,
workshop
organizers,
speakers.
Marine Environmental Research,
Journal Year:
2025,
Volume and Issue:
208, P. 107160 - 107160
Published: April 17, 2025
The
Mediterranean
Sea,
a
global
biodiversity
hotspot,
is
increasingly
threatened
by
anthropogenic
pressures,
leading
to
decline
in
marine
and
ecosystem
services.
In
response,
effective
monitoring
conservation
strategies,
including
citizen
science
initiatives,
are
crucial
for
understanding
mitigating
these
impacts.
This
study
presents
the
Marine
Adventure
Research
Education
(M.A.R.E.)
initiative,
which
integrates
public
participation
through
visual
surveys
environmental
DNA
(eDNA)
sampling.
Novel
species-specific
primers
were
developed
target
key
species,
Risso's
dolphin,
fin
whale,
basking
shark,
loggerhead
sea
turtle,
sperm
whale.
Over
three
months,
approximately
100
participants
contributed
detection
of
endangered
striped
Tyrrhenian
Sea.
Thus,
eDNA
analysis
proved
be
highly
sensitive
non-invasive
method
detecting
wide
range
complementing
traditional
surveys.
As
matter
fact,
second
most
detected
species
with
molecular
analyses
was
an
elusive
previously
underreported
region.
this
suggests
that
technique
might
considered
promising
monitor
dolphin
distribution
Analytical Sciences,
Journal Year:
2023,
Volume and Issue:
39(10), P. 1711 - 1718
Published: June 16, 2023
Environmental
RNA
(eRNA)
analysis
is
expected
to
infer
species'
physiological
information
(health
status,
developmental
stage,
and
environmental
stress
response)
their
distribution
composition
more
correctly
than
DNA
(eDNA)
analysis.
With
the
prospect
of
such
eRNA
applications,
there
an
increasing
need
for
technological
development
efficient
detection
because
its
physicochemical
instability.
The
present
study
conducted
a
series
aquarium
experiments
using
zebrafish
(Danio
rerio)
validated
methodologies
capture,
preservation,
extraction
in
water
sample.
In
experiment,
approximately
1.5-fold
increase
lysis
buffer
volume
resulted
sixfold
target
concentration.
capture
although
GF/F
GF/A
filters
yielded
similar
concentrations,
filter
may
be
capable
passing
through
samples
consequently
collecting
particles,
given
time
required
filtration.
preservation
use
stabilization
reagent
(RNAlater)
allowed
stably
preserving
on
sample
at
−
20
even
4
°C
6
days
least.
Altogether,
findings
enable
improvement
availability
from
field
easily
preserve
without
deep-freezing,
which
will
contribute
refinement
biological
monitoring
aquatic
ecosystems.
Environmental DNA,
Journal Year:
2024,
Volume and Issue:
6(2)
Published: March 1, 2024
Abstract
Environmental
RNA
(eRNA)
has
the
potential
as
a
non‐invasive
tool
for
assessing
physiological
status
of
macro‐organisms,
yet
quantitative
method
relative
gene
expression
analysis
is
still
underexplored.
To
bridge
this
gap,
study
introduces
quantification
eRNA,
employing
PCR
(qPCR)
to
evaluate
antioxidant
gene,
catalase
(
cat
),
in
Japanese
medaka
Oryzias
latipes
exposed
two
toxic
chemicals
96
h:
chlorpyrifos
(CPS)
and
carbamazepine.
Our
results
showed
that,
genes
frequently
used
reference
tissue
or
cells
conventional
correlated
with
each
other.
Also,
one
them
elfa
)
exhibited
less
variability,
showing
its
suitability
eRNA
analyses.
Additionally,
levels
increased
increasing
CPS
concentrations,
concentration‐response
manner.
These
suggest
promising
qPCR
applications
monitoring
an
organism's
health
response
environmental
changes.
However,
we
observed
disparities
beta‐actin
actb
between
whole
fish
body,
indicating
might
have
biased
origin.
Further
research
needed
uncover
origin
determine
limitations
applicability
domain
analysis.
Canadian Journal of Fisheries and Aquatic Sciences,
Journal Year:
2024,
Volume and Issue:
unknown
Published: June 10, 2024
Environmental
deoxyribonucleic
acid
(eDNA)
metabarcoding
offers
advantages
over
physical
capture
for
identifying
and
quantifying
animals
in
monitoring
programs.
In
this
study,
the
fish
community
was
sampled
at
three
stations
(inner,
middle,
outer
estuary)
estuaries
August
2020,
four
June
2021
(Prince
Edward
Island,
Canada)
using
both
beach
seining
eDNA
metabarcoding.
Two
12S
primer
sets,
12S-160
12S-248F,
with
different
amplicon
lengths,
yielded
similar
results.
consistently
detected
species
captured
by
186
co-located
seines
revealed
additional
species.
It
also
monthly
(June–August),
interannual
(2020–2021),
spatial
shifts
community,
distinguishing
separated
as
little
0.4
km.
Positive
correlations
existed
between
reads
captures.
These
findings
suggest
complements
methods
characterizing
nearshore
communities
Prince
Island’s
estuaries.
While
techniques
lack
certain
population
parameter
information
provided
methods,
such
size,
sex,
age
structure,
they
offer
a
more
comprehensive
diversity
assessment
presence–abundance
insights,
especially
inaccessible
environments.
Environmental DNA,
Journal Year:
2024,
Volume and Issue:
6(4)
Published: July 1, 2024
Abstract
Marine
mammal
foraging
grounds
are
popular
focal
points
for
marine
protected
area
(MPA)
implementation,
despite
being
temporally
dynamic,
requiring
continuous
monitoring
to
infer
prey
availability
and
abundance.
distributions
assumed
be
driven
by
their
in
areas,
but
limited
understanding
of
often
prevents
us
from
exploring
how
shifting
impacts
both
seasonal
long‐term
distributions.
Environmental
DNA
(eDNA)
metabarcoding
could
enhance
the
habitat
use
relation
through
simultaneous
both.
However,
eDNA
applications
focused
on
mammals
or
predator–prey
dynamics
have
been
date.
In
this
study,
we
assess
spatiotemporal
changes
distribution
abundance
cetaceans,
minke
whales
(
Balaenoptera
acutorostrata
),
bottlenose
dolphins
Tursiops
truncatus
)
harbor
porpoises
Phocoena
phocoena
key
species
a
newly
established
MPA,
employing
metabarcoding.
We
recovered
105
molecular
operational
taxonomic
units
(OTUs)
vertebrates
using
two
primer
sets
targeting
12S
16S
genes,
along
with
112
OTUs
broader
eukaryotic
set
18S
rRNA.
Overall,
forage
fish
species,
sandeels
clupeids,
were
most
abundant
teleost
fishes
detected,
although
varied
distance
shore.
also
found
clear
spatial
partitioning
between
coastal
more
pelagic
porpoises,
paralleling
main
species.
Other
conservation
interest
detected
including
critically
endangered
European
eel
Anguilla
anguilla
Atlantic
bluefin
tuna
Thunnus
thynnus
invasive
pink
salmon
Oncorhynchus
gorbuscha
).
This
study
demonstrates
application
detect
trends
occurrence
cetacean
predators
prey,
furthering
our
fine‐scale
within
MPAs.
Future
improve
ability
predict
climate‐induced
shifts
rapid
responses
appropriate
management
actions.
Environmental DNA,
Journal Year:
2024,
Volume and Issue:
6(4)
Published: July 1, 2024
Abstract
Environmental
DNA
(eDNA)
has
recently
emerged
as
an
effective
tool
for
invasive
species
biosecurity.
We
explored
the
use
of
eDNA
detection
khapra
beetle
(
Trogoderma
granarium
,
Everts
1898),
insect
cereal
grains
and
other
food
products
that
a
high
global
economic
impact.
developed
novel
method
aggregating
deposited
in
stored
grain
entails
washing
sample
rice,
filtering
sample,
detecting
trace
using
standard
qPCR
workflow.
To
explore
performance
this
method,
we
raised
500
larvae
within
g
rice
over
14‐day
period
then
removed
them.
used
“spiked”
to
create
range
simulated
densities
larvae.
This
lab
approach
mimics
conditions
are
comparable
field
~1.4
180
beetles
per
50
kg
(1/8
16
spiked
100
clean
rice),
assuming
is
uniformly
distributed
rice.
detected
from
all
density
levels
tested.
Logistic
models
revealed
amounts
equivalent
what
left
by
~1
larva
container
can
be
with
85%
>97%
certainty,
depending
on
number
technical
replicates
run
sample.
Based
model,
estimated
one
where
distributed,
single
six
would
sufficient
>99%
certain
was
free
(95%
credible
intervals:
97.7%–100%).
Our
results
suggest
surveys
may
useful
cost‐effective,
first‐step
provide
means
map
relative
magnitude
transport
pathways,
informing
allocation
conventional
biosecurity
inspection
efforts.
Biological Invasions,
Journal Year:
2024,
Volume and Issue:
26(11), P. 3715 - 3731
Published: July 24, 2024
Abstract
The
global
marine
ecosystem
is
changing
rapidly
as
the
result
of
biogeochemical
cycles
and
structure
being
altered
by
industrial
civilization.
Invasive
species
(IMS)
are
one
most
damaging
regional
consequences
human
activity,
easily
attributable
to
specific
processes.
This
makes
IMS
introduction
tractable
threats
for
management
appropriate
policies.
Once
established,
a
different
set
policies
required
either
restrict
spread,
or
attempt
local
eradication.
key
tool
damage
mitigation
rapid,
widely
deployable
detection.
Environmental
Nucleic
Acids
(eNA),
combining
environmental
DNA
(eDNA)
RNA
(eRNA)
analyses,
have
emerged
valuable
tools
sensitive,
cost-effective
readily
detection
IMS.
Methods
eNA
still
developed
through
widespread
active
research
community,
so
identifying
limitations
current
processes
will
help
prioritise
eNA-based
research.
We
analysed
synthesised
opinions
expert
managers
researchers
in
Australia
New
Zealand
about
knowledge
gaps
needs
synthesis
was
placed
context
with
literature
on
what
technologies
currently
providing
an
tool;
problems
exist
technology;
could
be
done
improve
this
general
approach.
Our
analyses
produced
list
priorities
that
chart
path
towards
best
possible
systems
eNA.