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Document Description
Title
Habitat
complexity
influences
the
growth
rate
of
juvenile
gadiformes
(gadus
morhua
,
gadus
ogac
,
urophysis
tenuis)
in
newman
sound
,
Newfoundland
Author
Renkawitz
,
Mark
D.
Description
Thesis
(M.Sc.)--Memorial
University
of
Newfoundland
,
2009.
Biology
Date
2008
Pagination
xvii, 152 leaves : ill.
Subject
Gadiformes--Newfoundland
and
Labrador--Newman
Sound--Growth;
Gadiformes--Newfoundland
and
Labrador--Newman
Sound--Habitat;
Marine
ecology--Newfoundland
and
Labrador--Newman
Sound;
Degree
M.Sc.
Degree Grantor
Memorial University of Newfoundland. Dept. of Biology
Discipline
Biology
Language
Eng
Spatial Coverage
Canada--Newfoundland and Labrador--Newman Sound
Notes
Includes
bibliographical
references
(leaves
89-106)
Abstract
In
Newman
Sound
,
Newfoundland
,
juvenile
fish
settle
in
shallow
near-shore
waters
and are
often
associated
with
eelgrass
beds
of
intermediate
structural
complexity.
Although
it
is
well
established
that
structurally
complex
habitats
such
as
eelgrass
provide
a
refuge
for
juvenile
fish
from
larger
predatory
fish
,
little
is
known
about
the
potential
energetic
reward
associated
with
use
of these
complex
habitats.
The
settlement
and
close
association
of
age
0
and
1
juvenile
fish
(approximately
60-100
mm
SL)
with
eelgrass
habitat
may
be the
result
of an
active
compromise
in
which
optimal
foraging
habitat
is
sacrificed
for
habitats
with
increased
shelter
from
predators.
In this
study
,
I
quantified
the
relative
growth
rates
of
fishes
associated
with
three
adjacent
habitats
of
differing
structural
complexity
(barren
seafloor
,
eelgrass
, and
water
column)
at
five
sites
in
Newman
Sound
,
Newfoundland.
Juvenile
Greenland
cod
(
Gadus
ogac
)
,
Atlantic
cod
(G.
morhua
)
, and
white
hake
(Urophysis
tenuis
)
were
placed
in
1
m
3
enclosures
positioned
over
eelgrass
,
barren
seafloor
, and
water
column
habitats
in
2002
and
2003.
Changes
in
standard
fish
length
(mm
SL)
and
volume
(ml)
were
measured
, and
specific
daily
growth
rates
were
determined
and
compared.
Stomach
contents
were
examined
for
habitat-related
differences
in the
type
and
quantity
of
items
consumed
by
enclosed
fish
at the
termination
of
each
experiment.
Zooplankton
samples
were also
collected
biweekly
during
summer
and
fall
in
2003
to
determine
if
differences
in
prey
concentration
differed
among
the
habitats.
--
Annual
and
seasonal
variations
in
growth
rates
were
documented
among
habitats
and
between
the
species.
In
fall
2002
, there was
no
statistical
difference
in
specific
growth
rates
(SGR)
of
Greenland
cod
among
the
habitats
(barren
=
0.068
%
SL·day-1
,
eelgrass
=
0.074
%
SL·day
-1
,
water
column
=
0.064
%
SL·day-1
).
SGR
of
Atlantic
cod
during
winter
from
2002
to
2003
did
not
differ
significantly
either
(barren
=
0.129
%
SL·day-1
,
eelgrass
=
0.151
%
SL·day-1
,
deep
water
=
0.116
%
SL·day
-1
)
, but
survival
was
significantly
greater
in
deeper
habitats
(55
%)
than in
shallower
habitats
(20
%).
In
spring
2003
,
mean
SGR
(±
SE)
of
Atlantic
cod
was
significantly
greater
in
eelgrass
than
barren
seafloor
or
water
column
habitats
(0.366
±
0.026
%
SL·day
-1
,
0.327
±
0.035
%
SL·day-1
, and
0.065
±
0.013
%
SL·day-1
respectively).
In
summer
2003
juvenile
white
hake
grew
more
rapidly
in
eelgrass
(0.713
±
0.062
%
SL·day
-1
)
than in
barren
or
water
column
habitats
(0.483
±
0.055
%
SL·day-1
and
0.271
±
0.040
%
SL·day
-1
respectively).
In
fall
2003
,
juvenile
Greenland
cod
grew
more
rapidly
in
water
column
(0.449
±
0.055
%
SL·day-1
)
habitats
than in
either
barren
(0.372
±
0.028
%
SL·day-1
)
or
eelgrass
habitats
(0.254
±
0.013
%
SL·day-1
).
Diets
were
similar
among
habitats
within
experiments
, but
differed
over
time.
Fish
in
eelgrass
tended
to have
greater
amount
of
food
by
weight
in their
stomachs
at the
time
of
sampling
than
fish
in
either
barren
or
water
column
habitats
(1.03
%
,
0.88
%
and
0.69
%
respectively).
Gadiformes
in
each
habitat
appeared
to
select
for
benthic
or
epibenthic
prey.
The
concentration
of
available
prey
differed
among
the
habitats.
Eelgrass
samples
had the
highest
concentration
of
zooplankton
(1.93
individuals·Liter
-1
)
,
followed
by
barren
(1.33
individuals·Liter-1
)
and
water
column
samples
(0.99
individuals·Liter-1
).
--
These
data
suggest
that at
certain
times
of the
year
,
juvenile
fish
settle
and
occupy
structurally
complex
habitats
for
energetic
reward
as
measured
by
growth.
At the
scale
of these
experiments
, there were
differences
in the
growth
rates
,
food
availability
and
zooplankton
concentration
between
three
habitats
at
my
sites.
Enclosure
methodology
can
be a
useful
tool
in
determining
relative
differences
between
specific
juvenile
fish
foraging
habitats
provided
that
confounding
variables
and
artifacts
of the
experimental
method
are
rigorously
accounted
for.
Understanding
the
relationships
between
specific
habitat
components
(e.g.
,
vegetation)
and
fish
growth
aids
our
understanding
of
juvenile
fish
ecology
, and
may
ultimately
help
restore
depleted
fish
populations
in the
Northwest
Atlantic
through
habitat
conservation
and
protection.
Type
Text
Resource Type
Electronic
thesis
or
dissertation
Format
Image/jpeg;
Application/pdf
Source
Paper copy kept in the Centre for Newfoundland Studies, Memorial University Libraries
Local Identifier
a3183778
Rights
The author retains copyright ownership and moral rights in this thesis. Neither the thesis nor substantial extracts from it may be printed or otherwise reproduced without the author's permission.
Collection
Electronic
Theses
and
Dissertations
Scanning Status
Completed
PDF File
(19.40
MB)
--
http://collections.mun.ca/PDFs/theses/Renkawitz_MarkD.pdf
CONTENTdm file name
57628.cpd