Diversity,
Journal Year:
2024,
Volume and Issue:
16(5), P. 306 - 306
Published: May 20, 2024
Habitat
selection
has
been
a
central
focus
of
animal
ecology,
with
research
primarily
concentrating
on
habitat
choice,
utilization,
and
evaluation.
However,
studies
confined
to
single
scale
often
fail
reveal
the
needs
animals
fully
accurately.
This
paper
investigates
wintering
whooper
swan
(Cygnus
cygnus)
in
Manas
National
Wetland
Park,
Xinjiang,
using
satellite
tracking
determine
their
locations.
The
Maximum
Entropy
model
(MaxEnt)
was
applied
explore
multi-scales
Park’s
swans
across
nighttime,
daytime,
landscape
scales.
study
showed
that
varied
different
At
scale,
prefer
habitats
average
winter
precipitations
6.9
mm
temperatures
−6
°C,
including
water
bodies
wetlands,
indicating
climate
(precipitation
temperature)
land
type
(wetlands
bodies)
influence
selection.
During
areas
close
bodies,
bare
land,
more
dispersed
distribution
bodies.
For
they
tend
choose
within
wetland
park
where
human
disturbance
is
minimal
safety
higher.
can
provide
scientific
basis
data
support
for
conservation
management
waterbirds
like
swans,
recommending
targeted
measures
effectively
manage
protect
grounds
swans.
Biological reviews/Biological reviews of the Cambridge Philosophical Society,
Journal Year:
2023,
Volume and Issue:
98(3), P. 868 - 886
Published: Jan. 23, 2023
ABSTRACT
Spatial
and
social
behaviour
are
fundamental
aspects
of
an
animal's
biology,
their
spatial
environments
indelibly
linked
through
mutual
causes
shared
consequences.
We
define
the
‘spatial–social
interface’
as
intersection
individuals'
phenotypes
environments.
Behavioural
variation
at
spatial–social
interface
has
implications
for
ecological
evolutionary
processes
including
pathogen
transmission,
population
dynamics,
evolution
systems.
link
a
foundation
theory,
vocabulary,
methods.
provide
examples
future
directions
integration
introduce
key
concepts
approaches
that
either
implicitly
or
explicitly
integrate
processes,
example,
graph
density‐dependent
habitat
selection,
niche
specialization.
Finally,
we
discuss
how
movement
ecology
helps
interface.
Our
review
integrates
behavioural
identifies
testable
hypotheses
Journal of Animal Ecology,
Journal Year:
2020,
Volume and Issue:
90(1), P. 45 - 61
Published: Sept. 28, 2020
Abstract
Social
network
analysis
has
achieved
remarkable
popularity
in
disease
ecology,
and
is
sometimes
carried
out
without
investigating
spatial
heterogeneity.
Many
investigations
into
sociality
may
nevertheless
be
subject
to
cryptic
variation,
so
ignoring
processes
can
limit
inference
regarding
dynamics.
Disease
analyses
gain
breadth,
power
reliability
from
incorporating
both
social
behavioural
data.
However,
the
tools
for
collecting
analysing
these
data
simultaneously
complex
unintuitive,
it
often
unclear
when
variation
must
accounted
for.
These
difficulties
contribute
scarcity
of
simultaneous
spatial‐social
ecology
thus
far.
Here,
we
detail
scenarios
that
benefit
analysis.
We
describe
procedures
collection
data,
outline
statistical
approaches
control
estimate
covariance
analyses.
hope
researchers
will
expand
more
include
components
questions.
measures
increase
scope
such
analyses,
allowing
accurate
model
estimates,
better
transmission
modes,
susceptibility
effects
contact
scaling
patterns,
ultimately
effective
interventions.
Journal of Animal Ecology,
Journal Year:
2022,
Volume and Issue:
91(7), P. 1334 - 1344
Published: April 7, 2022
Abstract
Individual
decisions
regarding
how,
why
and
when
organisms
interact
with
one
another
their
environment
scale
up
to
shape
patterns
processes
in
communities.
Recent
evidence
has
firmly
established
the
prevalence
of
intraspecific
variation
nature
its
relevance
community
ecology,
yet
challenges
associated
collecting
data
on
large
numbers
individual
conspecifics
heterospecifics
have
hampered
integration
into
ecology.
Nevertheless,
recent
technological
statistical
advances
GPS‐tracking,
remote
sensing
behavioural
ecology
offer
a
toolbox
for
integrating
processes.
More
than
simply
describing
where
go,
movement
provide
unique
information
about
interactions
environmental
associations
from
which
true
individual‐to‐community
framework
can
be
built.
By
linking
paths
both
data,
ecologists
now
simultaneously
quantify
interspecific
Eltonian
(biotic
interactions)
Grinnellian
(environmental
conditions)
factors
underpinning
assemblage
dynamics,
substantial
logistical
analytical
must
addressed
these
approaches
realize
full
potential.
Across
communities,
empirical
support
conservation
applications
reveal
metacommunity
dynamics
via
tracking‐based
dispersal
data.
As
multi‐species
tracking
are
surmounted,
we
envision
future
movements
ecological
signatures
will
bring
resolution
many
enduring
issues
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2020,
Volume and Issue:
unknown
Published: June 14, 2020
Abstract
Animal
tracking
data
are
being
collected
more
frequently,
in
greater
detail,
and
on
smaller
taxa
than
ever
before.
These
hold
the
promise
to
increase
relevance
of
animal
movement
for
understanding
ecological
processes,
but
this
potential
will
only
be
fully
realized
if
their
accompanying
location
error
is
properly
addressed.
Historically,
coarsely-sampled
have
proved
invaluable
large
scale
processes
(e.g.,
home
range,
habitat
selection,
etc.),
modern
fine-scale
unlock
far
information.
While
GPS
can
often
ignored
coarsely
sampled
data,
require
care,
tools
do
not
kept
pace.
Current
approaches
dealing
with
largely
fall
into
two
categories—either
discarding
least
accurate
estimates
prior
analysis
or
simultaneously
fitting
parameters
a
hidden-state
model.
In
some
cases
these
provide
level
correction,
they
known
limitations,
worse
doing
nothing.
Here,
we
general
framework
account
triangulated
trilatcralizcd
which
includes
GPS,
Argos
Doppler-shift,
VHF,
trilatcralized
acoustic
cellular
data.
We
apply
our
error-modelselection
190
cellular,
devices
representing
27
models
from
14
manufacturers.
Collectively,
were
used
track
wide
range
comprising
birds,
fish,
reptiles,
mammals
different
sizes
behaviors,
urban,
suburban,
wild
settings.
almost
half
tested
device
models,
error-model
selection
was
necessary
obtain
best
performing
model,
quarter
reported
DOP
values
actually
misinformative.
Then,
using
empirical
multiple
species,
an
overview
modern,
error-informed
analyses,
including
continuous-time
path
reconstruction,
home-range
distribution,
overlap,
speed,
distance
estimation.
Adding
techniques,
introduce
new
estimators
outlier
detection
autocorrelation
visualization.
Because
error-induced
biases
depend
many
factors—sampling
schedule,
characteristics,
device,
habitat,
etc.—differential
bias
easily
confound
biological
inference
lead
researchers
draw
false
conclusions.
demonstrate
how
analyses
calibrated
that
insensitive
error,
allow
use
all
Methods in Ecology and Evolution,
Journal Year:
2022,
Volume and Issue:
14(8), P. 1887 - 1905
Published: Oct. 11, 2022
Abstract
GPS‐based
tracking
is
widely
used
for
studying
wild
social
animals.
Much
like
traditional
observational
methods,
using
GPS
devices
requires
making
a
number
of
decisions
about
sampling
that
can
affect
the
robustness
study's
conclusions.
For
example,
fewer
individuals
per
group
across
more
distinct
groups
may
not
be
sufficient
to
infer
group‐
or
subgroup‐level
behaviours,
while
limits
ability
draw
conclusions
populations.
Here,
we
provide
quantitative
recommendations
when
designing
studies
animal
societies.
We
focus
on
trade‐offs
between
three
fundamental
axes
effort:
(1)
coverage—the
and
allocation
among
in
one
groups;
(2)
duration—the
total
amount
time
over
which
collect
data
(3)
frequency—the
temporal
resolution
at
record
data.
first
test
tags
under
field
conditions
quantify
how
these
aspects
design
both
accuracy
(error
absolute
positional
estimates)
precision
estimate
relative
position
two
individuals),
demonstrating
error
have
profound
effects
inferring
distances
individuals.
then
use
from
whole‐group
tracked
vulturine
guineafowl
Acryllium
vulturinum
demonstrate
trade‐off
frequency
duration
impact
inferences
interactions
coverage
common
measures
behaviour
groups,
identifying
types
are
less
robust
lower
Finally,
data‐informed
simulations
extend
insights
different
sizes
cohesiveness.
Based
our
results,
able
offer
range
strategies
address
research
questions
organizational
scales
systems—from
movement
network
structure
collective
decision‐making.
Our
study
provides
practical
advice
empiricists
navigate
their
decision‐making
processes
highlights
importance
optimal
deployment
drawing
informative
Ecology Letters,
Journal Year:
2022,
Volume and Issue:
25(5), P. 1290 - 1304
Published: March 8, 2022
The
ongoing
explosion
of
fine-resolution
movement
data
in
animal
systems
provides
a
unique
opportunity
to
empirically
quantify
spatial,
temporal
and
individual
variation
transmission
risk
improve
our
ability
forecast
disease
outbreaks.
However,
we
lack
generalizable
model
that
can
leverage
how
it
affects
pathogen
invasion
persistence
on
heterogeneous
landscapes.
We
developed
flexible
'Movement-driven
modelling
spatio-temporal
infection
risk'
(MoveSTIR)
leverages
diverse
derive
metrics
direct
indirect
contact
by
decomposing
into
constituent
processes
formation
duration
deposition
acquisition.
use
MoveSTIR
demonstrate
ignoring
fine-scale
movements
actual
landscapes
mis-characterize
epidemiological
dynamics.
unifies
previous
work
networks
address
applied
theoretical
questions
at
the
nexus
ecology.
Ecology and Evolution,
Journal Year:
2023,
Volume and Issue:
13(3)
Published: March 1, 2023
Abstract
Quantifying
spatiotemporally
explicit
interactions
within
animal
populations
facilitates
the
understanding
of
social
structure
and
its
relationship
with
ecological
processes.
Data
from
tracking
technologies
(Global
Positioning
Systems
[“GPS”])
can
circumvent
longstanding
challenges
in
estimation
interactions,
but
discrete
nature
coarse
temporal
resolution
data
mean
that
ephemeral
occur
between
consecutive
GPS
locations
go
undetected.
Here,
we
developed
a
method
to
quantify
individual
spatial
patterns
interaction
using
continuous‐time
movement
models
(CTMMs)
fit
data.
We
first
applied
CTMMs
infer
full
trajectories
at
an
arbitrarily
fine
scale
before
estimating
thus
allowing
inference
occurring
observed
locations.
Our
framework
then
infers
indirect
interactions—individuals
same
location,
different
times—while
identification
vary
context
based
on
CTMM
outputs.
assessed
performance
our
new
simulations
illustrated
implementation
by
deriving
disease‐relevant
networks
for
two
behaviorally
differentiated
species,
wild
pigs
(
Sus
scrofa
)
host
African
Swine
Fever
mule
deer
Odocoileus
hemionus
chronic
wasting
disease.
Simulations
showed
derived
be
substantially
underestimated
when
exceeds
30‐min
intervals.
Empirical
application
suggested
underestimation
occurred
both
rates
their
distributions.
CTMM‐Interaction
method,
which
introduce
uncertainties,
recovered
majority
true
interactions.
leverages
advances
ecology
fine‐scale
spatiotemporal
individuals
lower
It
leveraged
dynamic
networks,
transmission
potential
disease
systems,
consumer–resource
information
sharing,
beyond.
The
also
sets
stage
future
predictive
linking
environmental
drivers.
Ecological Monographs,
Journal Year:
2022,
Volume and Issue:
92(3)
Published: March 24, 2022
Abstract
Home
ranges
(HRs),
the
regions
within
which
animals
interact
with
their
environment,
constitute
a
fundamental
aspect
of
ecology.
HR
sizes
and
locations
commonly
reflect
costs
benefits
associated
diverse
social,
biotic,
abiotic
factors.
Less
is
known,
however,
about
how
these
factors
affect
intraspecific
variation
in
size
or
fidelity
(the
individual's
tendency
to
maintain
same
location
over
time)
whether
features
emerge
from
consistent
differences
among
individuals
sites
they
occupy.
To
address
this
knowledge
gap,
we
used
an
extensive
GPS‐tracking
data
set
long‐lived
lizard,
sleepy
lizard
(
Tiliqua
rugosa
),
included
repeated
observations
multiple
across
years.
We
tested
three
categories
predictors—(1)
characteristics
(sex,
aggressiveness,
parasitic
tick
counts),
(2)
environmental
(precipitation,
food,
refuge
quality),
(3)
social
conditions
(conspecific
overlap
number
neighbors)—affected
fidelity.
found
that
differed
consistently
annual
HRs
(with
repeatability
0.58
0.33,
respectively),
all
predictors
affected
both
For
example,
were
smaller
areas
more
males
had
larger
than
females.
In
addition,
aggressive
lizards
tended
have
HRs.
Conspecific
interacted
(social
network
degree)
interactive
effect
on
where
whose
overlapped
neighbors
HRs,
was
particularly
strong
for
neighbors.
declined
time
(HR
drifted
year
year),
but
rate
drift.
The
fact
despite
drifting
suggests
individual
traits
(e.g.,
habitat
choice
criteria
differ
individuals),
rather
simple
heterogeneity
sites.
Overall,
findings
demonstrate
(1)
strong,
long‐term,
within‐individual
consistency
between‐individual
space
use
combined
effects
traits,
conditions,
animal
implications
ecological
processes.