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Introduction
In the University of Saskatchewan work, nearcontinuous light impacted growth rate negatively
when birds were weighed at 32 (Figure 1), 39
(Figure 2) and 49 d (Figure 3) of age (British Poultry
Science, in press). At 32 d (quadratic relationship
between daylength and weight), body weight peaked
when birds were exposed to 20L. A shift occurred
in this pattern as birds aged. At 39 d, the heaviest
body weights were still found 20L, but 17L birds
outweighed 20L birds (quadratic relationship). This
trend continued, and at 49 d, birds raised under 17
and 20L were heaviest, and even birds exposed to 14L
were heavier than those under 23L. Thus, it appears
that darkness exposure slows growth early in life,
but broilers have the ability to adapt with resulting
increased growth later in life. When birds were grown
to heavier weights, adding even more darkness to the
photoperiod program resulted in similar body weights
as achieved under 4 h of darkness.
1,75
Karen Schwean-Lardner
32d
kg
1,70
1,65
1,60
1,55
14L
17L
20L
23L
XXIV
2,35
39d
kg
2,25
2,20
2,15
14L
17L
20L
23L
Karen Schwean-Lardner
kg
49d
14L
17L
20L
23L
0,70
2,30
3,28
3,26
3,24
3,22
3,20
3,18
3,16
3,14
3,12
3,10
7-32d
7-39d
7-49d
0,65
0,70
7-32d
7-39d
7-49d
0,65
0,60
0,60
0,55
0,55
0,50
0,50
14L
17L
20L
23L
14L
17L
20L
23L
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7-32d
7-39d
2,0
7-49d
% mortality
7
6
%
5
4
3
2
1
1,5
Metabolic
Skeletal
1,0
0,5
0,0
0
14L
17L
20L
14L
23L
17L
20L
23L
17L
20L
23L
SEM
28 d
2.34
2.34
4.69
0.730
35 d
0.63
2.50
4.33
0.413
45 d
4.66
9.26
8.72
16.26
1.117
2,5
Metabolic
2,0
Skeletal
1,5
1,0
0,5
0,0
3,0
Metabolic
2,5
Skeletal
Karen Schwean-Lardner
% mortality
% mortality
2,0
1,5
1,0
0,5
0,0
14L
17L
20L
23L
XXIV
17L
20L
23L
31 d
Absolute (g)
46 d
Absolute (g)
Karen Schwean-Lardner
17L
20L
23L
SEM
31 d
Carcass
65.90
66.27 66.38
66.25
0.138
Total breast
17.24
17.64 17.99
18.21
0.128
Drum meat
3.16
3.09
3.04
2.99
0.020
Carcass
67.25
68.04 68.63
68.63
0.110
Total breast
14.92
15.51 15.93
16.19
0.107
Drum meat
3.23
3.16
3.10
3.07
0.012
Carcass
70.42
71.14 72.34
71.58
0.189
Total breast
19.99
20.62 21.29
21.14
0.130
Drum meat
3.25
3.18
3.11
0.018
38 d
49 d
3.14
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90
10
60
4
17L
20L
14L
23L
17L
20L
5
27d
42d
27d
4
% time
4
3
2
23L
% time
70
14L
27d
42d
80
% time
% time
27d
42d
42d
3
2
0
14L
17L
20L
23L
14L
17L
20L
1,2
0,6
27d
27d
% time
% time
0,2
42d
0,9
42d
0,4
23L
Karen Schwean-Lardner
0,6
0,3
0,0
0,0
14L
17L
20L
23L
14L
17L
20L
23L
XXIV
% time
27d
42d
4
2
0
14L
17L
20L
23L
Karen Schwean-Lardner
14L
17L
20L
23L
Inactive resting
Walking
Standing
Feeding
Drinking
Preening
Dustbathing
Conclusions
The results of this research demonstrate
that daylength has important effects on broiler
productivity, which in turn affect the economics
of production. With the exception of breast meat
yield, near-constant lighting programs have no
advantages in comparison to other daylengths tested
for broiler production. Furthermore, the loss of body
weight and increase in mortality may outweigh the
economic advantages of increased breast muscle.
Lighting programs using 20 h light and 4 h darkness
(20L) result in intermediate performance heavier
body weights at the younger ages of 31/32 d, but
with little or no differences as compared to longer
dark periods at older ages. Once again, mortality is
higher than when longer dark periods, such as the
17L program used here, are employed. These data
indicate that in terms of productivity, choosing an
exact lighting program for all situations may not be
ideal. Age of marketing, cost of feed ingredients,
historical farm mortality rates and farm altitude are
some of the examples that might be considered
when choosing an appropriate daylength to include
in a lighting program.
The data also indicate that daylength has a
vital importance in dictating the well-being of
broilers. The poor growth rate of birds raised on
23L indicates a welfare problem, and the higher
mortality is a major welfare issue. Behavioural
expression suffers to a point of extreme lethargy
under very long daylengths, and the near loss of
important behaviours such as nutritive, comfort
and exploratory behaviours indicate poor well-being
as well. Loss of flock synchrony in behaviour and
melatonin production signal abnormal behavioural
and physiological functioning, furthering this
argument. Reducing daylength to 20L improves
XXIV
100
80
60
40
20
0
0
200
400
600
800
1000
1200
1400
1600
1800
2000
2200
2400
Figure 17a - Percent of flock inactive resting of birds on 14L:10D at d 27. The black checked line represents the
scotophase period, and the green triangle line the photophase. Behaviour responded quadratically with time
during the photophase (P=0.0001).
100
80
60
40
20
0
0
200
400
600
800
100
80
60
40
20
0
0
200
400
600
800
Karen Schwean-Lardner
Figure 17b - Percent of flock inactive resting of birds on 17L:7D at 27 d. The black line represents the
scotophase period, and the green line the photophase. Behaviour responded quadratically over time during the
photophase (P=0.0001).
Figure 17c - Percent of flock inactive resting of birds on 20L:4D at 27 d. The black line represents the
scotophase period, and the green line the photophase. Daytime relationship between behaviour and time was
not statistically significant.
100
80
60
40
20
0
0
200
400
600
800
Figure 17d - Percent of flock inactive resting of birds on 23L:1D at 27 d. The black line represents the
scotophase period, and the green line the photophase. Daytime relationship between behaviour and time was
not statistically significant.
Area: Chicken Breeder and Broiler Production August 06
XXIV
Melatonin (pg/ml)
160
140
120
100
80
60
40
20
0
0
300
600
900
1200
1500
1800
2100
2400
Melatonin (pg/ml)
Figure 18a - Melatonin rhythm of birds raised on 14L:10D at d21. The black line represents the scotophase
period, and the green line the photophase. Serum melatonin levels respond quadratically over the 24 h period
(P=0.0001).
160
140
120
100
80
60
40
20
0
0
300
600
900
1200
1500
1800
2100
2400
160
140
Melatonin (pg/ml)
Karen Schwean-Lardner
Figure 18b - Melatonin rhythm of birds raised on 17L:7D at d 21. Serum melatonin levels respond quadratically
over the 24 h period (P=0.0001).
120
100
80
60
40
20
0
0
300
600
900
1200
1500
1800
2100
2400
Melatonin (pg/ml)
Figure 18c - Melatonin rhythm of birds raised on 20L:4D at d 21. Serum melatonin levels respond quadratically
the 24 h period (P=0.0154).
160
140
120
100
80
60
40
20
0
0
300
600
900
1200
1500
1800
2100
2400
Figure 18d - Melatonin rhythm of birds raised on 23L:1D at d 21. The 24 h period relationship between
behaviour and time was not statistically significant (P=0.9447).
XXIV
Acknowledgements
While it has been shown that birds can sleep
during the light period, the quality of that sleep is
likely poorer (Rattenborg et al., 2005). Beyond that,
flocks that do not follow a synchronized pattern of
behavioural expression very likely may waken birds
that are attempting to sleep during the photophase.
This is termed sleep fragmentation, and in other
species, has been shown to be as detrimental as
total sleep deprivation (Chen and Kushida, 2005).
In this research, flocks under 23L did not form
synchronized behavioural patterns during the
photophase for any behaviour monitored, which
makes the development of sleep fragmentation
possible. Similarly, 20L flocks only exhibited
synchronized patterns in some behaviours. Those on
14L and 17L were synchronized in their behavioural
expression. Strengthening the argument of sleep
deprivation was the impact of daylength on
melatonin production. Melatonin plays an important
part in the onset of sleep, driven partly by the height
of the night-time peak, the duration of the peak,
and the range between the peak and valley. Under
23L, no synchronized rhythms were noted, showing
that levels did not differ between photo- and
scotophases periods. Functions of sleep are many,
including tissue regeneration, energy restoration,
immune function, memory development, mental
Karen Schwean-Lardner
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Karen Schwean-Lardner
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