Fisheries Science,
Journal Year:
2019,
Volume and Issue:
85(2), P. 327 - 337
Published: Jan. 3, 2019
Abstract
Environmental
DNA
(eDNA)
consists
of
fragments
shed
from
organisms
into
the
environment,
and
can
be
used
to
identify
species
presence
abundance.
This
study
aimed
reveal
dispersion
degradation
processes
eDNA
in
sea.
Caged
fish
were
set
off
end
a
pier
Maizuru
Bay,
Sea
Japan,
their
was
traced
at
sampling
stations
located
cage
10,
30,
100,
300,
600
1000
m
distances
along
two
transect
lines.
surface
water
collected
each
station
0,
2,
4,
8,
24
48
h
after
setting
cage,
again
removing
cage.
Quantitative
PCR
analyses
using
species-specific
primer
probe
revealed
that
target
detectable
while
present
for
up
1
but
not
2
or
later.
Among
57
amplified
samples,
45
(79%)
within
30
These
results
suggest
provide
snapshot
coastal
marine
environment.
Environmental DNA,
Journal Year:
2021,
Volume and Issue:
4(1), P. 9 - 33
Published: Feb. 25, 2021
Abstract
Environmental
DNA
(eDNA)
has
revolutionized
our
ability
to
identify
the
presence
and
distributions
of
terrestrial
aquatic
organisms.
Recent
evidence
suggests
concentration
eDNA
could
also
provide
a
rapid,
cost‐effective
indicator
abundance
and/or
biomass
for
fisheries
stock
assessments.
Globally,
resources
are
under
immense
pressure,
their
sustainable
harvest
requires
accurate
information
on
sizes
fished
stocks.
However,
in
many
cases
required
remains
elusive
because
reliance
imprecise
or
costly
fishery‐dependent
independent
data.
Here,
we
review
literature
describing
relationships
between
concentrations
fish
biomass,
as
well
key
influencing
factors,
precursor
determining
broader
utility
monitoring
populations.
We
reviewed
63
studies
published
2012
2020
found
90%
identified
positive
focal
species.
Key
biotic
factors
included
taxon
examined
body
size,
distribution,
reproduction,
migration.
abiotic
mostly
comprised
hydrological
processes
affecting
dispersal
persistence
eDNA,
especially
water
flow
temperature,
although
collection
methods
were
influential.
The
cumulative
influence
these
different
likely
explains
substantial
variability
observed
concentrations,
both
within
among
studies.
Nevertheless,
there
is
considerable
support
using
an
ancillary
tool
assessing
population
across
discrete
spatio‐temporal
scales,
following
preliminary
investigations
determine
species‐
context‐specific
abundance/biomass
relationship.
Advantages
relative
other
approaches
include
reduced
costs,
increased
efficiencies,
nonlethal
sampling.
Molecular Ecology,
Journal Year:
2018,
Volume and Issue:
28(2), P. 407 - 419
Published: June 25, 2018
Abstract
DNA
metabarcoding
is
a
technique
used
to
survey
biodiversity
in
many
ecological
settings,
but
there
are
doubts
about
whether
it
can
provide
quantitative
results,
that
is,
the
proportions
of
each
species
mixture
as
opposed
list.
While
several
experimental
studies
report
similar
number
fail
do
so.
Here,
we
rationale
understand
under
what
circumstances
be
quantitative.
In
essence,
simulate
S
with
defined
initial
abundance
distribution.
simulated
PCR
,
increases
its
concentration
following
certain
amplification
efficiency.
The
final
will
reflect
one
when
efficiency
for
all
species;
otherwise,
and
concentrations
would
poorly
related.
Although
known
factors
modulate
efficiency,
focused
on
primer–template
mismatches,
arguably
most
important
one.
We
15
common
primers
pairs
targeting
mitochondrial
COI
region
mitogenomes
ca
.
1,200
insect
species.
results
showed
some
produced
circumstances,
whereas
other
failed
conclusion,
depending
primer
pair
characteristics
analysed
(i.e.,
high
richness,
low
evenness),
estimate
relative
abundances
different
PLoS ONE,
Journal Year:
2017,
Volume and Issue:
12(4), P. e0176343 - e0176343
Published: April 25, 2017
Molecular
analysis
of
environmental
DNA
(eDNA)
can
be
used
to
assess
vertebrate
biodiversity
in
aquatic
systems,
but
limited
work
has
applied
eDNA
technologies
marine
waters.
Further,
there
is
understanding
the
spatial
distribution
Here,
we
use
an
metabarcoding
approach
target
and
amplify
a
hypervariable
region
mitochondrial
12S
rRNA
gene
characterize
communities
at
10
oceanographic
stations
spanning
45
km
within
Monterey
Bay
National
Marine
Sanctuary
(MBNMS).
In
this
study,
collected
three
biological
replicates
small
volume
water
samples
(1
L)
2
depths
each
stations.
We
amplified
fish
using
universal
primer
set.
obtained
5,644,299
high
quality
Illumina
sequence
reads
from
samples.
The
were
annotated
lowest
taxonomic
assignment
bioinformatics
pipeline.
survey
identified,
rank,
7
families,
3
subfamilies,
genera,
72
species
vertebrates
study
sites.
These
92
distinct
taxa
come
33
unique
families.
observed
significantly
different
community
composition
between
sampling
(0
m
20/40
deep)
across
all
located
on
continental
shelf
(<200
bottom
depth)
versus
deeper
waters
canyons
(>200
depth).
All
1
family
identified
known
occur
MBNMS.
informs
implementation
for
biomonitoring.
Conservation Biology,
Journal Year:
2018,
Volume and Issue:
33(1), P. 196 - 205
Published: July 13, 2018
Abstract
Monitoring
communities
of
fish
is
important
for
the
management
and
sustainability
fisheries
marine
ecosystems.
Baited
remote
underwater
video
systems
(BRUVs)
are
among
most
effective
nondestructive
techniques
sampling
bony
fishes
elasmobranchs
(sharks,
rays,
skates).
However,
BRUVs
sample
visually
conspicuous
biota;
hence,
some
taxa
undersampled
or
not
recorded
at
all.
We
compared
diversity
characterized
using
with
detected
via
environmental
DNA
(eDNA)
metabarcoding.
sampled
seawater
captured
imagery
48
locales
that
included
reef
seagrass
beds
inside
outside
a
reserve
(Jurien
Bay
in
Western
Australia).
Eighty‐two
genera
from
13
orders
were
detected,
community
described
eDNA
combined
yielded
>30%
more
generic
richness
than
when
either
method
was
used
alone.
Rather
detecting
homogenous
genetic
signature,
assemblages
mirrored
BRUVs’
spatial
explicitness;
differentiation
between
clear
despite
relatively
small
geographical
scale
study
site
(∼35
km
2
).
Taxa
by
one
approach,
due
to
limitations
biases
intrinsic
method,
often
other.
Therefore,
concert
provides
holistic
view
vertebrate
across
habitats.
Both
methods
noninvasive,
which
enhances
their
potential
widespread
implementation
surveillance
Molecular Ecology,
Journal Year:
2020,
Volume and Issue:
29(6), P. 1069 - 1086
Published: Feb. 11, 2020
Environmental
DNA
(eDNA)
metabarcoding,
a
technique
for
retrieving
multispecies
from
environmental
samples,
can
detect
diverse
array
of
marine
species
filtered
seawater
samples.
There
is
growing
potential
to
integrate
eDNA
alongside
existing
monitoring
methods
in
order
establish
or
improve
the
assessment
diversity.
Remote
island
reefs
are
increasingly
vulnerable
climate-related
threats
and
as
such
there
pressing
need
cost-effective
whole-ecosystem
surveying
baseline
biodiversity,
study
assemblage
changes
ultimately
develop
sustainable
management
plans.
We
investigated
utility
metabarcoding
high-resolution,
multitrophic
biomonitoring
tool
at
Cocos
(Keeling)
Islands,
Australia
(CKI)-a
remote
tropical
coral
reef
atoll
situated
within
eastern
Indian
Ocean.
Metabarcoding
assays
targeting
mitochondrial
16S
rRNA
CO1
genes,
well
18S
nuclear
gene,
were
applied
252
surface
samples
collected
42
sites
140
km2
area.
Our
successfully
detected
wide
range
bony
fish
elasmobranchs
(244
taxa),
crustaceans
(88),
molluscs
(37)
echinoderms
(7).
Assemblage
composition
varied
significantly
between
sites,
reflecting
habitat
partitioning
across
ecosystem
demonstrating
localisation
signals,
despite
extensive
tidal
oceanic
movements.
In
addition,
we
document
putative
new
occurrence
records
46
taxa
compare
efficiency
our
approach
visual
survey
techniques
CKI.
demonstrates
multimarker
capturing
biodiversity
an
entire
sets
important
ongoing
management.
Fish and Fisheries,
Journal Year:
2018,
Volume and Issue:
19(5), P. 751 - 768
Published: April 6, 2018
Abstract
Application
of
environmental
DNA
(e
)
analysis
has
attracted
the
attention
researchers,
advisors
and
managers
living
marine
resources
biodiversity.
The
apparent
simplicity
cost‐effectiveness
e
make
it
highly
attractive
as
species
distributions
can
be
revealed
from
water
samples.
Further,
species‐specific
analyses
indicate
that
concentrations
correlate
with
biomass
abundance,
suggesting
possibility
for
quantitative
applications
estimating
abundance
specific
organisms
in
ecosystems,
such
stock
assessment.
However,
path
detecting
occurrence
an
organism
to
estimates
is
long
indirect,
not
least
concentration
depends
on
several
physical,
chemical
biological
factors
which
influence
its
production,
persistence
transport
ecosystems.
Here,
we
provide
overview
basic
principles
relation
potential
fisheries
application.
We
describe
fundamental
processes
governing
generation,
breakdown
summarize
current
uncertainties
about
these
processes.
five
major
challenges
application
assessment,
where
there
immediate
need
knowledge
building
systems,
point
weaknesses
compared
established
monitoring
methods.
emerging
interest
management
recent
technological
advances,
could
improve
efficiency.
advise
precaution
against
exaggerating
present
scope
monitoring,
but
also
argue
informed
insights
into
strengths
limitations,
become
integrated
tool
assessment
management.
Ecology and Evolution,
Journal Year:
2018,
Volume and Issue:
8(12), P. 6330 - 6341
Published: May 29, 2018
Environmental
DNA
(eDNA)
analysis
is
a
rapid,
cost-effective,
non-invasive
biodiversity
monitoring
tool
which
utilises
left
behind
in
the
environment
by
organisms
for
species
detection.
The
method
used
as
species-specific
survey
rare
or
invasive
across
broad
range
of
ecosystems.
Recently,
eDNA
and
"metabarcoding"
have
been
combined
to
describe
whole
communities
rather
than
focusing
on
single
target
species.
However,
whether
metabarcoding
sensitive
targeted
approaches
detection
remains
be
evaluated.
great
crested
newt
Triturus
cristatus
flagship
pond
international
conservation
concern
first
UK
routinely
monitored
using
eDNA.
We
evaluate
has
comparable
sensitivity
real-time
quantitative
PCR
(qPCR)
T.
Extracted
samples
(N
=
532)
were
screened
qPCR
analysed
all
vertebrate
high-throughput
sequencing
technology.
With
threshold
1
12
positive
replicates,
newts
detected
50%
ponds.
Detection
decreased
32%
when
was
increased
4
replicates.
metabarcoding,
34%
ponds
without
threshold,
28%
(0.028%)
applied.
Therefore,
provided
greater
but
with
no
equivalent
stringent
threshold.
proportion
sequences
each
sample
positively
associated
number
replicates
(qPCR
score)
suggesting
may
indicative
concentration.
holds
enormous
potential
holistic
assessment
routine
freshwater
monitoring.
advocate
this
community
approach
guide
management
conservation,
whereby
entire
can
initially
surveyed
best
inform
use
funding
time
surveys.
PLoS ONE,
Journal Year:
2017,
Volume and Issue:
12(4), P. e0175186 - e0175186
Published: April 12, 2017
The
difficulty
of
censusing
marine
animal
populations
hampers
effective
ocean
management.
Analyzing
water
for
DNA
traces
shed
by
organisms
may
aid
assessment.
Here
we
tested
aquatic
environmental
(eDNA)
as
an
indicator
fish
presence
in
the
lower
Hudson
River
estuary.
A
checklist
local
and
their
relative
abundance
was
prepared
compiling
12
traditional
surveys
conducted
between
1988-2015.
To
improve
eDNA
identification
success,
31
specimens
representing
18
species
were
sequenced
two
mitochondrial
gene
regions,
boosting
coverage
12S
target
sequence
to
80%
taxa.
We
collected
76
one-liter
shoreline
surface
samples
at
contrasting
estuary
locations
over
six
months
beginning
January
2016.
amplified
with
vertebrate-specific
primers.
Bioinformatic
analysis
DNA,
using
a
reference
library
GenBank
our
newly
generated
sequences,
detected
most
(81%)
locally
abundant
or
common
relatively
few
(23%)
uncommon
taxa,
corresponded
seasonal
habitat
preference
determined
surveys.
Approximately
2%
reads
commonly
consumed
that
are
rare
absent
waters,
consistent
wastewater
input.
Freshwater
rarely
despite
inflow.
These
results
support
further
exploration
suggest
will
facilitate
fine-scale
geographic
temporal
mapping
low
cost.
Genes,
Journal Year:
2019,
Volume and Issue:
10(3), P. 192 - 192
Published: March 1, 2019
Population
genetic
data
underpin
many
studies
of
behavioral,
ecological,
and
evolutionary
processes
in
wild
populations
contribute
to
effective
conservation
management.
However,
collecting
samples
can
be
challenging
when
working
with
endangered,
invasive,
or
cryptic
species.
Environmental
DNA
(eDNA)
offers
a
way
sample
material
non-invasively
without
requiring
visual
observation.
While
eDNA
has
been
trialed
extensively
as
biodiversity
biosecurity
monitoring
tool
strong
taxonomic
focus,
it
yet
fully
explored
means
for
obtaining
population
information.
Here,
we
review
current
research
that
employs
approaches
the
study
populations.
We
outline
challenges
facing
eDNA-based
methodologies,
suggest
avenues
future
developments.
advocate
further
optimizations,
this
emergent
field
holds
great
potential
part
genetics
toolkit.