Frontiers in Marine Science,
Journal Year:
2023,
Volume and Issue:
10
Published: Feb. 27, 2023
Species
detection
using
environmental
DNA
(eDNA)
is
a
biomonitoring
tool
that
can
be
widely
applied
to
mangrove
restoration
and
management.
Compared
traditional
surveys
are
taxa-specific
time-consuming,
eDNA
metabarcoding
offers
rapid,
non-invasive
cost-efficient
method
for
monitoring
biodiversity
characterising
the
spatio-temporal
distribution
of
multiple
taxa
simultaneously.
General
guidelines
well-established
aquatic
systems,
but
habitat-specific
still
lacking.
Mangrove
habitats,
as
priority
ecosystems
in
Southeast
Asia,
present
unique
prospects
challenges
these
regards.
Environmental
used
(1)
track
functional
recovery
ecological
restoration,
(2)
prioritise
conservation
areas,
(3)
provide
early
warning
threats,
(4)
monitor
threatened
taxa,
(5)
response
climate
change,
(6)
support
community-based
restoration.
However,
potential
applications
have
yet
been
realized
Asia
due
technical
challenges,
lack
standardised
methods,
difficulties
defining
community,
data
limitations,
funding,
infrastructure
capacity.
Successful
implementation
activities
would
encourage
development
data-driven
coastal
management
equitable
programs.
Eventually,
this
promote
Asia’s
shared
regional
interests
food
security,
defence
conservation.
The Science of The Total Environment,
Journal Year:
2023,
Volume and Issue:
873, P. 162322 - 162322
Published: Feb. 18, 2023
Environmental
DNA
(eDNA)
is
the
fastest
growing
biomonitoring
tool
fuelled
by
two
key
features:
time
efficiency
and
sensitivity.
Technological
advancements
allow
rapid
biodiversity
detection
at
both
species
community
levels
with
increasing
accuracy.
Concurrently,
there
has
been
a
global
demand
to
standardise
eDNA
methods,
but
this
only
possible
an
in-depth
overview
of
technological
discussion
pros
cons
available
methods.
We
therefore
conducted
systematic
literature
review
407
peer-reviewed
papers
on
aquatic
published
between
2012
2021.
observed
gradual
increase
in
annual
number
publications
from
four
(2012)
28
(2018),
followed
growth
124
This
was
mirrored
tremendous
diversification
methods
all
aspects
workflow.
For
example,
freezing
applied
preserve
filter
samples,
whereas
we
recorded
12
different
preservation
2021
literature.
Despite
ongoing
standardisation
debate
community,
field
seemingly
moving
fast
opposite
direction
discuss
reasons
implications.
Moreover,
compiling
largest
PCR-primer
database
date,
provide
information
522
141
species-specific
metabarcoding
primers
targeting
wide
range
organisms.
works
as
user-friendly
'distillation'
primer
that
hitherto
scattered
across
hundreds
papers,
list
also
reflects
which
taxa
are
commonly
studied
technology
environments
such
fish
amphibians,
reveals
groups
corals,
plankton
algae
under-studied.
Efforts
improve
sampling
extraction
specificity
reference
databases
crucial
capture
these
ecologically
important
future
surveys.
In
rapidly
diversifying
field,
synthetises
procedures
can
guide
users
towards
best
practice.
Pensoft Publishers eBooks,
Journal Year:
2021,
Volume and Issue:
unknown
Published: Dec. 2, 2021
DNA-based
methods
for
species
detection
and
identification
have
revolutionised
our
ability
to
assess
biodiversity
in
terrestrial,
freshwater
marine
ecosystems.
Starting
from
the
seminal
study
that
used
eDNA
detect
invasive
american
bullfrogs
France
(Gentile
Francesco
Ficetola
et
al.
2008)),
research
conducted
over
last
decade
has
demonstrated
power
of
these
approaches
surveying
a
wide
range
groups.
Early
applications
included
use
monitor
Asian
Carp
USA
(Jerde
2013).
Following
heavy
scrutiny,
method
was
eventually
adopted,
is
still
employed
today
by
United
States
Geological
Survey
(USGS).
A
flurry
followed,
with
tests
designed
many
threatened
including
New
zealand
mudsnails
(Goldberg
2013),
crayfish
(Geerts
2018),
gammarids
(R.
Blackman
2017),
great
crested
newts
(Biggs
2015).
The
newt
test
been
regulatory
monitoring
UK
since
2014.
During
same
time
period,
there
proliferation
studies
high-throughput
sequencing
describe
whole
communities
organisms
mixed
environmental
samples,
using
an
approach
termed
DNA
metabarcoding
(Taberlet
2012).
Environmental Science & Technology,
Journal Year:
2022,
Volume and Issue:
56(9), P. 5322 - 5333
Published: April 18, 2022
Increased
use
of
environmental
DNA
(eDNA)
analysis
for
indirect
species
detection
has
spurred
the
need
to
understand
eDNA
persistence
in
environment.
Understanding
is
complex
because
it
exists
a
mixture
different
states
(e.g.,
dissolved,
particle
adsorbed,
intracellular,
and
intraorganellar),
each
state
expected
have
specific
decay
rate
that
depends
on
parameters.
Thus,
improving
knowledge
about
conversion
rates
between
reactions
degrade
needed.
Here,
we
focus
eukaryotic
extraorganismal
eDNA,
outline
how
water
chemistry
suspended
mineral
particles
likely
affect
among
state,
indicate
parameters
column.
On
basis
deducing
these
controlling
parameters,
synthesized
literature
assess
whether
could
already
derive
general
understanding
persisting
However,
found
are
often
not
being
measured
or
reported
when
measured,
many
cases
very
few
experimental
data
exist
from
which
draw
conclusions.
Therefore,
further
study
aquatic
environments
We
recommend
analytic
controls
can
be
used
during
processing
potential
losses
if
all
were
present
sample,
future
work
would
help
determine
dominant
water.
BMC Bioinformatics,
Journal Year:
2021,
Volume and Issue:
22(1)
Published: April 5, 2021
The
recent
blooming
of
metabarcoding
applications
to
biodiversity
studies
comes
with
some
relevant
methodological
debates.
One
such
issue
concerns
the
treatment
reads
by
denoising
or
clustering
methods,
which
have
been
wrongly
presented
as
alternatives.
It
has
also
suggested
that
denoised
sequence
variants
should
replace
clusters
basic
unit
analyses,
missing
fact
are
a
proxy
for
species-level
entities,
in
studies.
We
argue
here
methods
developed
and
tested
ribosomal
markers
uncritically
applied
highly
variable
cytochrome
oxidase
I
(COI)
without
conceptual
operational
(e.g.,
parameter
setting)
adjustment.
COI
naturally
high
intraspecies
variability
be
assessed
reported,
it
is
source
valuable
information.
contend
not
Rather,
they
complementary
both
used
together
pipelines.Using
dataset
from
benthic
marine
communities,
we
compared
two
procedures
(based
on
UNOISE3
DADA2
algorithms),
set
suitable
parameters
clustering,
these
steps
different
orders.
Our
results
indicated
algorithm
preserved
higher
intra-cluster
variability.
introduce
program
DnoisE
implement
taking
into
account
natural
(measured
entropy)
each
codon
position
protein-coding
genes.
This
correction
increased
number
sequences
retained
88%.
order
(denoising
clustering)
had
little
influence
final
outcome.We
highlight
need
combining
adequate
choice
stringency
parameters,
metabarcoding.
present
uses
coding
properties
this
marker
improve
step.
recommend
researchers
report
their
terms
(a
haplotypes)
formed
species),
avoid
collapsing
latter
single
representative.
will
allow
at
cluster
(ideally
equating
diversity)
level,
ease
additivity
comparability
between
Environmental DNA,
Journal Year:
2022,
Volume and Issue:
4(4), P. 894 - 907
Published: April 11, 2022
Abstract
Analysis
of
environmental
DNA
is
increasingly
used
to
characterize
ecological
communities,
but
the
effectiveness
this
approach
depends
on
accuracy
taxonomic
reference
databases.
The
MIDORI
databases,
first
released
in
2017,
were
built
improve
for
mitochondrial
metazoan
(animal)
sequences.
has
now
been
significantly
improved
and
renamed
MIDORI2
(available
at
http://www.reference‐midori.info
).
Like
MIDORI,
from
GenBank
contains
curated
sequences
thirteen
protein‐coding
two
ribosomal
RNA
genes.
Coverage
substantially
expanded
cover
all
eukaryotes,
including
fungi,
green
algae
land
plants,
other
multicellular
algal
groups,
diverse
protist
lineages.
also
includes
not
only
species
with
full
binomials,
taxa
referred
by
genus
left
unspecified
(“sp.”).
Another
new
feature
updating
databases
approximately
every
months
version
numbers
corresponding
each
release.
Additional
potentially
erroneously
annotated
have
removed.
Finally,
ability
export
data
files
BLAST+
added
original
preformatted
five
assignment
programs,
amino
acid
are
made
available
As
a
technical
validation,
we
conducted
preliminary
comparison
performance
programs.
Results
suggest
that
top
hits
performed
better
assigning
CO1
than
alignment‐free
methods
based
compositional
features.
Comparing
commonly
sequences,
CO‐ARBitrator
BOLD,
show
broader
range
non‐metazoan
taxa.
Overall,
many
contexts,
offers
clear
advantages:
higher
diversity
variety
user‐friendly
features,
regular
updates.
particularly
well‐suited
studies
target
genes
broad
primers.
Estuaries and Coasts,
Journal Year:
2022,
Volume and Issue:
45(7), P. 2254 - 2273
Published: June 25, 2022
Abstract
Environmental
DNA
(eDNA)
detection
methods
can
complement
traditional
biomonitoring
to
yield
new
ecological
insights
in
aquatic
systems.
However,
the
conceptual
and
methodological
frameworks
for
eDNA
interpretation
were
developed
primarily
freshwater
environments
have
not
been
well
established
estuaries
marine
that
are
by
nature
dynamic,
turbid,
hydrologically
complex.
context
species
life
history
critical
successful
application
of
methods,
challenges
associated
with
subject
a
symposium
held
at
University
California
Davis
on
January
29,
2020
(
https://marinescience.ucdavis.edu/engagement/past-events/edna
).
Here,
we
elaborate
upon
topics
addressed
evaluate
monitoring
biodiversity
studies
estuaries.
We
first
provide
concise
overview
science
then
examine
San
Francisco
Estuary
(SFE)
as
case
study
illustrate
how
programs
regional
guidance
future
potential
applications.
Additionally,
offer
recommendations
enhancing
communication
between
scientists
natural
resource
managers,
which
is
essential
integrating
into
existing
programs.
Our
intent
create
accessible
those
outside
field
eDNA,
especially
without
oversimplifying
or
advantages
these
methods.
Molecular Ecology Resources,
Journal Year:
2022,
Volume and Issue:
23(2), P. 396 - 409
Published: Sept. 24, 2022
Environmental
DNA
(eDNA)
metabarcoding
is
an
effective
method
for
studying
fish
communities
but
allows
only
estimation
of
relative
species
abundance
(density/biomass).
Here,
we
combine
with
the
total
eDNA
amplified
by
our
universal
marker
(teleo)
using
a
quantitative
(q)PCR
approach
to
infer
absolute
species.
We
carried
out
2850-km
survey
within
Danube
catchment
spatial
integrative
sampling
protocol
coupled
traditional
electrofishing
biomass
and
density
estimation.
Total
concentrations
were
highly
correlated.
The
correlation
between
per
taxon
specific
was
comparable
strength
when
all
sites
pooled
remained
significant
considered
separately.
Furthermore,
nonlinear
mixed
model
showed
that
richness
underestimated
amount
teleo-DNA
extracted
from
sample
below
threshold
0.65
×
10
Methods in Ecology and Evolution,
Journal Year:
2022,
Volume and Issue:
14(2), P. 415 - 430
Published: April 12, 2022
Abstract
Several
studies
have
shown
the
potential
of
eDNA‐based
proxies
for
plant
identification,
but
little
is
known
about
their
spatial
and
temporal
resolution.
This
limits
its
use
biodiversity
assessments
monitoring
vegetation
responses
to
environmental
changes.
Here
we
calibrate
signals
detected
with
soil
eDNA
surveys
by
comparing
a
standard
visual
above‐ground
survey.
Our
approach
compares
in
an
old‐growth
boreal
forest
southern
Norway,
surveyed
100
permanent
1‐m
2
plots
seven
times
over
30‐year
period,
single
metabarcoding‐based
survey
from
samples
collected
at
same
year
last
On
average,
60%
10%
vascular
plants
bryophytes
recorded
across
all
were
eDNA.
Taxa
more
representative
local
taxa
pool
than
specific
plot,
corresponded
those
period
although
most
closely
matched
current
composition.
Soil
abundant
better
rare
ones
both
unrecorded
detected.
study
highlights
broad
scales.
The
method's
ability
detect
makes
it
suitable
assessment
composition
area
broad‐scale
diversity
assessments.
Environmental DNA,
Journal Year:
2023,
Volume and Issue:
5(4), P. 671 - 682
Published: May 16, 2023
Abstract
Reliable
and
comparable
estimates
of
biodiversity
are
the
foundation
for
understanding
ecological
systems
informing
policy
decision‐making,
especially
in
an
era
massive
anthropogenic
impacts
on
biodiversity.
Environmental
DNA
(eDNA)
metabarcoding
is
at
forefront
technological
advances
monitoring,
last
few
years
have
seen
major
progress
solutions
to
technical
challenges
from
laboratory
bioinformatics.
Water
eDNA
has
been
shown
allow
fast
efficient
recovery
signals,
but
rapid
pace
development
meant
that
some
important
principles
regarding
sampling
design,
which
well
established
traditional
inventories,
neglected.
Using
a
spatially
explicit
river
flow
model,
we
illustrate
how
must
be
adjusted
size
watercourse
increase
quality
signal
recovered.
We
additionally
investigate
effect
parameters
(volume,
number
sites,
sequencing
depth)
detection
probability
empirical
data
set.
Based
principles,
propose
aquatic
replication
volume
scaled
match
organisms'
ecosystems'
properties
provide
reliable
estimates.
present
generalizable
conceptual
equation
describing
features
as
function
ecosystem
monitored,
abundance
target
organisms,
procedure.
The
aim
this
formalization
enhance
standardization
critical
steps
design
inventory
studies
using
eDNA.
More
robust
standards
will
generate
more
eDNA,
necessary
method's
long‐term
plausibility
comparability.