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In the past five years it has become apparent that dairy heifer
and cow function can be modified by alterations in the indoor
lighting conditions and recommendations have been made regarding
light intensity and duration of light exposure during the day. Some
of these recommendations, which are meant to increase milk
production, can result in inconvenience for the dairy producer and
an increase in the cost of barn lighting. As well, unanswered
questions regarding barn lighting conditions still remain. The
studies described herein were designed to provide answers which
would help to ensure that, with respect to dairy barn lighting
conditions, convenience for the dairy producer is maximized,
lighting cost is minimized and milk production is not compromised in
any way.
In Experiment 1 we examined the effect of various intensities of
dim light on dairy heifer physiology and in Experiment 2 we examined
the effect of various day lengths on milk production of dairy cows.
The results have been previously published in the M.Sc. Thesis of
Pushpa Mutharamalingam.
Experiment 1 - Plasma Melatonin and
IGF-1 Responses to Dim Light at Night in Prepubertal Dairy Heifers
Background:
Melatonin hormone is produced by the pineal gland
of the brain only at night. This results in the very regular
occurrence of high levels of melatonin in the blood (a high plateau in
cattle) at night and levels of essentially zero during the day for a
wide variety of species. This daily rhythm in blood melatonin is
thought to direct other daily rhythms in the body and is thought to be
important for good animal health. Light intensities of 150 to 200 Lux
are recommended during daytime as studies (reviewed by Dahl et al.
2000) have shown that dairy cattle respond to such intensities with an
increase in milk production when the day length is extended to 16 to
18 hours.
Through previous Manitoba Hydro and ARDI funding,
we (Lawson and Kennedy 2001) have previously shown that a light
intensity of 50 Lux causes a reduction in night melatonin level in
dairy heifers but lower intensities of light were not examined. Dahl
et al. (2000) have emphasized that 6 to 8 hours of complete darkness
is important for dairy cows to ensure the continuation of natural
circadian rhythms. Manitoba Hydro also makes this recommendation when
advising dairy producers on lighting retrofits or new barn lighting.
At this point we can only say that the use of a 50 Lux light intensity
at night will likely shorten the length of the night perceived by
dairy cows and so may be bad with respect to milk production and cow
health. Dahl et al. (2000) recommends only red light be used at
night, if a night light is needed. Most species, including cattle, do
not respond to light in the red end of the visible spectrum. This
recommendation has generally not been accepted in the industry as it
is not practical.
Many dairy farmers still provide either dim light
(less than 100 Lux) or bright light (greater than 100 Lux) at night to
promote feed consumption at night and to facilitate health checks
during the night. Although research has shown that bright night light
does not promote feeding at night (Tanida et al. 1984) and that it may
actually decrease feed intake (Peters et al. 1981), the practice
continues. Because there have never been studies showing negative
production effects of dim light at night, the practice of the use of
dim light is considered acceptable by many producers.
Animal species differ dramatically in their
sensitivity to light with the highest sensitivity being found,
logically, in nocturnal species. Theoretically, for every species,
there is an intensity of light or limit of sensitivity, below which
the animal will demonstrate no physiological response to the light.
This level in sheep (Arendt and Ravault 1988) is very low (1.0 Lux or
lower) but sensitivity to dim light in cattle has not been previously
studied using very dim levels of light. Thus, we do not know what the
"safe" intensity of dim nightlight for cattle is. Our previous
research (Lawson and Kennedy 2001) suggested that the intensity was
below 50 Lux.
Objective:
To determine if low light intensities have a physiological effect
in dairy heifers.
Experimental Approach:
Plasma melatonin levels were measured in dairy heifers exposed at
night (8 hours) for a short (1 day) and long (14 days) time to no dim
light (0 Lux), two very low intensities of dim light (5 and 10 Lux) or
an intensity of dim light (50 Lux) previously shown to cause a
physiological effect. The 5 and 10 Lux intensities were chosen as it
would be possible for dairy producers to check cows at these
intensities of light. An intensity of light less than 5 Lux would be
too dim for practical use.
Methods:
Twelve dairy heifers were exposed to 0, 5, 10 or 50 Lux (0, 0.5,
1.0 or 5 fc) light intensity during the 8 hour nighttime period for 14
consecutive days using a Latin Square Design which made it possible
for every heifer to receive every treatment once. Eric Witkowski,
lighting engineer, Manitoba Hydro, designed the incandescent and
fluorescent lighting schemes for four rooms in the Animal Science
Research Unit at the University of Manitoba for this experiment.
Fluorescent fixtures were used for lighting during the day and
incandescent fixtures were used for experimental lighting during the
night. Bulbs of a variety of wattages were used to achieve uniformity
in the dim light intensities required throughout the animal holding
areas. Blood samples were collected via jugular catheter during the
last hour of the light period and at 1, 2, 4 and 8 hours of the night
on days 1, 4 and 14 of the experiment. The heifers were exposed to a
light intensity of 200 Lux (20 fc) during the 16 hour days.
Results and Discussion:
Statistical analysis revealed that there was a significant
Treatment X Hour effect which is shown in Figure 1 where means
represent a particular hour averaged over days 1, 4 and 14 of the
experiment. Of the three light treatments, only the 50 Lux treatment
affected plasma melatonin level and this effect had disappeared by the
4th hour of the night. Plasma melatonin only rose to 50% of the
normal night level when the 50 Lux light was present at night.
Although the negative effect of 50 Lux on melatonin disappeared by 4
hours into the night, because melatonin analysis was done only on
samples collected at 2 and 4 hours of the night, the negative effect
may have lasted for 3 hours or more. This inhibitory effect of 50 Lux
was equally dramatic at l, 4 and 14 days of treatment. Because the
ability of 50 Lux to depress melatonin at night occurred consistently
throughout the 14 day experiment, we feel confident that the heifers
did not become insensitive to 50 Lux over time. This is important in
that one cannot assume that animals will "get over" the negative
effect of 50 Lux on plasma melatonin levels.
It is necessary to question whether there would be functional
consequences to a 50% reduction in plasma melatonin at night which was
caused by the 50 Lux treatment. Although this question cannot be
answered at this time, related information in sheep suggests that the
height of the nighttime melatonin plateau is of practical importance.
As found in sheep (Hotter and Chemineau 2001) we have observed a high
degree of variability among dairy heifers for the normal night level
of plasma melatonin. Some heifers consistently have a high plateau
while other consistently have a plateau ½ to ¼ the highest levels
found. In sheep, nighttime melatonin plateau levels are negatively
correlated to fertility (Hotter and Chemineau 2001). It would be very
interesting to examine this in cattle but as of yet this has not been
attempted.
Melatonin values at night for the 5 and 10 Lux treatments were not
different from values found during complete darkness (0 Lux) (Figure
1). Thus, the 0, 5 and 10 Lux treated heifers all showed the normal
rise in plasma melatonin at night. Unfortunately, we were limited to
having 4 treatments in this experiment and so were unable to test the
effects of the intermediate light intensities of 20, 30 and 40 Lux.
Results found on day 4 and 14 were identical to results found on day
1 indicating that the heifer sensitivity to 5 and 10 Lux does not
develop over time.
Our results indicate that dairy heifers are not sensitive to 5 or
10 Lux light during the night but respond to 50 Lux for greater than 2
but less than 4 hours per night. If light with an intensity of 50 Lux
is used at night in dairy barns, cows will receive less
"physiological" hours of darkness than intended, and possibly needed,
for good health. The heifers showed no tendency to develop either
increased or decreased sensitivity to dim light over the course of the
14 day experimental period. Dahl et al. (2000) has indicated that 6-8
hours of darkness is important for dairy cows in order to ensure the
continuation of natural circadian rhythms. Currently there are dairy
producers who provide light at 50 Lux or higher at night. In such
cases, the presence of light at night may be reducing the length of
night to shorter than that recommended. A recommendation for the use
of 5 or 10 Lux intensity at night in dairy barns would ensure that
light at night does not compromise cow productivity and health.
Conclusions:
Current recommendations are that it is important for dairy cattle
to be exposed to a certain number of hours of complete darkness each
night (at least 6 hours according to industry experts) but many dairy
producers leave lights on in the barn at night for a variety of
practical reasons. Our results indicate that a night light of 50 Lux
has a physiological impact on cattle but intensities of 5 and 10 Lux
do not. We were limited to having 4 treatments and so were unable to
test the effects of the intermediate light intensities of 20, 30 and
40 Lux. This study is the first in the world to study, under
controlled conditions, the effects of very low light intensities on
cattle physiology. The results suggest that farmers should be very
cautious when using light intensities greater than 10 Lux during the
night. Light of 10 Lux intensity is bright enough for humans, and
likely cattle, to see fairly well if the eyes are allowed a minute or
two to adapt. Thus, use of dim light up to 10 Lux in intensity is a
practical and safe alternative for dairy producers who wish to have
light in their free-stall or tie-stall barns during the night.
Experiment 2 - Milk
Production, Milk Composition and Plasma IGF-1 in Dairy Cows Exposed to
14, 16, 18, and 20 h Photoperiods
Background:
Dahl et al. (2000) reviewed a large number of studies where
exposure of dairy cows to 16 to 18 hour day length increases milk
production significantly compared to 13 or lower hours of day length.
They recommend that day length be no longer than 16 to 18 hours
(length of total darkness at night no shorter than 6 to 8 hours) in
order to ensure the continuation of natural circadian rhythms.
Manitoba Hydro also makes this recommendation when advising dairy
producers on lighting retrofits or new barn lighting. However, only
indirect evidence was used to conclude that day lengths longer than 18
can be deleterious to milk production and that 14 hours is too short
of a day to generate this effect. Having a day length as short as 14
hours or longer than 18 hours could be very convenient and/or
economical for dairy producers as they would have more flexibility in
management in terms of when lights must be turned off or on. This
could lead to a saving in hydro bills and bulb costs (use of a 14 hour
day) or result in improvements in ability to check the cows at night
(if it is safe to have lights on for 20 hours a day). Based on solid
evidence, exposure of dairy cows to light for 24 hours a day is not
recommended.
Twenty-four hour a day light exposure resulted in reduced feed
intake of dairy cows (Peters et al. 1981). Because milk production
using 14 or 20 hour day lengths has never been directly compared to
that using 16 or 18 h day lengths, a study was done to make this
comparison using lactating dairy cows.
Objectives:
To compare milk yield, milk composition, body weight, body
condition score, feed intake and plasma IGF-1 levels in lactating
dairy cows exposed to day lengths of 14 16, 18, and 20 hours.
Methods:
Milk composition, body weight, body condition score, feed intake
and plasma IGF-1 levels were measured in dairy cows exposed to day
lengths of 14, 16, 18 and 20 hours at the Glenlea Dairy Facility.
Twelve cows (4 primiparous and 8 multiparous, 109 ± 14 d in milk at
the start of the trial) were used but two were eliminated from the
study due to poor health. Breeding of the cows was synchronized so
that each would be in early lactation at the beginning of the study
which was 168 days in length. The cows weighed 695.6 ± 57.8 kg (mean
± SD). Cows had unlimited access to feed and water and were fed 1 kg
hd-1 d-1 of alfalfa hay (Table 1). The TMR was balanced for the
production of 35 kg of milk/day/cow. Cows were milked twice daily
(04:30 h and 16:30 h).
Table 1. Composition of the Diet for Experiment 2
|
Chemical Composition
(%) |
Alfalfa Hay |
Total Mixed Rationz |
|
Dry Matter |
87.5 |
48.8 |
|
Crude Protein |
7.6 |
18.3 |
|
Acid Detergent Fiber |
39.1 |
23.7 |
|
Neutral Detergent Fiber |
60.5 |
38.2 |
|
Net
Energy Lactation (NEL)y |
1.2 |
1.61 |
z Containing
(g kg-1): Alfalfa silage (315); Corn silage (320); Dairy 26 (260); DPE
(95); Sunflower Seed (10).
y Energy
content expressed as NEL (Mcal kg-1) (Cornell Nutrition Conference
1979 and Penn State Lab Nutrition 1978).
Each cow was given each treatment for 6 weeks using a Latin Square
Design. Administration of 4 lengths of day in the Glenlea tie-stall
barn was achieved by the use of polyethylene curtains that separated
cows, in treatment groups of three, from all other cows. Separate
light controls and fluorescent fixtures were installed for each of the
4 curtained areas to achieve a light intensity of approximately 250
Lux in each area during the day. The curtains were all raised in the
morning to allow milking and lowered in the evening so that some cows
could receive different day lengths.
Milk production was measure daily. Feed intake was measured over
the final 2 days of weeks 5 and 6 of each treatment. Milk samples
were collected during weeks 5 and 6 for analysis of milk fat, protein,
SNF and somatic cell count. The daily amount of TMR given to each
group of cows was recorded during periods 2, 3 and 4. Weigh backs for
each group were recorded weekly during weeks 1 to 4 and daily during
week 5 and week 6. Representative samples of the weigh backs and the
TMR were collected. Core samples of the hay were taken from each new
bale fed during experimental periods 2, 3 and 4. Daily samples of the
TMR and weigh backs were pooled for weeks 5 and 6 separately and hay
samples from all periods were pooled for proximate analysis.
Blood samples were collected by tail vein puncture on day 7 of week
3 and week 6 of each period using 10 ml heparinized vacutainer tubes
and 20 G needles for measurement of IGF-1 level. Body weight, body
condition score were conducted during the 6th week of each treatment.
Two cows were removed from trial, one due to an udder injury and
subsequent mastitis, and another due to a dramatic drop in milk yield
during period 2 of the trail. Data for these cows were not included
in the statistical analysis.
Milk samples were preserved with 2-bromo-2-nitropropane-1,3 diol
and stored at 4°C until analyzed for composition using near infrared
spectroscopy (NIR) with the Milk-O-Scan 303AB (Floss Electric,
Hillerod, Denmark) at the laboratory of the Manitoba Milk Producers
(Winnipeg, MB).
Dry matter content of both the feed and weighbacks was determined
by drying at 60°C for 48 h (AOAC, 1990). All feed samples were
analyzed for crude protein (Mixed Catalyst Kjeldahl procedure, AOAC,
1990), NDF (National Forage Testing Association, 1993) and ADF (AOAC,
1990). Ca, P, K, Mg and Na were measured using inductively coupled
plasma emission spectroscopy (AOAC, 1990). Feed efficiency (kg of
milk/kg of dry matter intake) was calculated for individual cows.
Plasma was collected after blood centrifugation (3000 x g for 30
minutes) and stored at - 20°C until assayed for IGF-1 (Kerr et al.
1990) at the Western College of Veterinary Medicine, Saskatoon, SK.
Analysis of variance was carried out to determine the significance
of treatment on the milk yield, milk composition, body weight, body
condition scoring, feed intake and plasma IGF-1 level. Statistical
analysis of the data was performed using Mixed Model procedure of SAS
(SAS Institute, Cary, NY, 1999). Initially, data for weeks 5 and 6 of
each period were analyzed separately, but was then averaged prior to
analysis, as the effect of week was not significant (P>0.05). Cows
were at 192 ± 15 (mean ± SD) days in milk by the beginning of period
4. It was considered that light treatments might not be as effective
on milk yield in late lactation as in mid- lactation. For this
reason, statistical analysis was performed with and without period 4
in the data set. In this analysis, because dry matter intake was
available for only periods 2 and 3, intake was not assessed
statistically but arithmetic means were calculated. All effects were
tested against the residual error. Initial milk yield (week 1) was
used as a covariate in the analysis, but was non-significant. Parity,
days of pregnancy and days in milk were used as covariates in the
model, but were dropped from subsequent analysis because treatment
effects in the covariate analysis remained non-significant even though
the covariates were found to be significant (P = 0.05).
Results and Discussion:
Body weight and body condition scoring did not differ among
treatments throughout the experiment. There was no effect of day
length on milk yield, dry matter intake and feed efficiency whether
results of 4 periods (Table 2) or 3 periods (Table 3) of the
experiment were analyzed. Thus, for these parameters, inclusion of
late lactation data (period 4, Table 3) made no difference. It must
be noted that the variation among treatments for milk yield was very
high (Tables 2 and 3). Because of this variation, at least a 25%
difference among treatments in milk yield would be required to be
significant. In a review, Dahl et al. (2000) indicated that the milk
response to long photoperiod (16 h) is sometimes only a 6% increase.
Such an increase would be very difficult to demonstrate using the
cows of the Glenlea dairy herd. At this point we can only conclude
that none of the day length treatments had a large effect on milk
production. The variability in our results suggests a number of
possible problems. To find moderate or low milk production
differences, we would need to use a large number of cows - more than
the 12 used in this study. It is also possible that the lack of
treatment differences related to the 6-week treatment period which
may have been too short to allow for a full photoperiodic response to
develop. However, others (Dahl et al. 1997) have seen a response in 4
weeks. Also, all other studies (reviewed by Dahl et al. 2000) used
cows which had been exposed to a short natural day length (<12 hours)
or a short artificial photoperiod (13 hours) prior to their studies.
Cows were exposed to an artificial 18 hour day prior to our study.
Table 2. Effect of Photoperiod on Milk Yield, Milk Composition and
Plasma IGF-1 Levels in Dairy Cows (Least Square Means) When All Four
Periods of the Experiment Were Included
|
Trait |
Photoperiod (hours/day) |
|
14 |
16 |
18 |
20 |
SEMz |
P = |
|
Milk Yield (kg/d) |
30.6 |
30.6 |
31.5 |
31.4 |
2.5 |
0.87 |
|
Milk Fat (kg/d) |
1.0 |
1.0 |
1.1 |
1.1 |
0.09 |
0.44 |
|
Milk Protein (kg/d) |
1.1 |
1.0 |
1.1 |
1.1 |
0.09 |
0.38 |
|
Dry Matter Intake (kg/d) |
20.7 |
21.0 |
21.8 |
20.3 |
0.83 |
0.27 |
|
Feed Efficiencyy |
1.4 |
1.4 |
1.4 |
1.5 |
0.08 |
0.71 |
|
Plasma IGF-1 (ng/ml) |
147 |
155 |
153 |
152 |
11 |
0.90 |
|
Body Weight (kg) |
715 |
705 |
710 |
716 |
19 |
0.42 |
|
Body Condition Score |
3.7 |
3.7 |
3.7 |
3.7 |
0.10 |
0.80 |
z SEM =
pooled standard error of the mean
y kg of
milk /kg of feed
Table 3. Effect of Photoperiod on Milk Yield, Milk Composition and
Plasma IGF-1 Levels in Dairy Cows (Least Square Means) When Only the
First Three Periods of the Experiment Were Included
|
Trait |
Photoperiod (hours/day) |
|
14 |
16 |
18 |
20 |
SEMz |
P = |
|
Milk Yield (kg/d) |
31.5 |
32.5 |
33.4 |
32.2 |
2.6 |
0.70 |
|
Milk Fat (kg/d) |
1.0 |
1.0 |
1.2 |
1.1 |
0.10 |
0.09 |
|
Milk Protein (kg/d) |
1.1 |
1.1 |
1.2 |
1.1 |
0.09 |
0.60 |
|
Dry Matter Intake (kg/d) |
22.0 |
21.3 |
22.7 |
20.0 |
NA |
NA |
|
Feed Efficiencyy |
1.5 |
1.4 |
1.5 |
1.4 |
0.11 |
0.45 |
|
Plasma IGF-1 (ng/ml) |
141 |
157 |
152 |
158 |
11 |
0.45 |
|
Body Weight (kg) |
710 |
704 |
708 |
715 |
16 |
0.68 |
|
Body Condition Score |
3.7 |
3.7 |
3.7 |
3.8 |
0.12 |
0.75 |
z SEM =
pooled standard error of the mean
y kg of
milk /kg of feed
Plasma IGF-1 concentration did not differ among treatments (Tables
2 and 3). The level of variation was similar to that found in other
studies where changes in day length did affect the plasma level of
IGF-1. It is thought that long photoperiod increases milk production
through the action of IGF-1 hormone. Spicer et al. (1994) found an
increase in the concentration of blood IGF-1 hormone in heifers
exposed to 16 hour (159 ng ml-1) and 18 hour (133 ng ml-1 ) compared
to 8 hour (111 ng ml-1) day lengths. A 24 hour day length resulted in
the same IGF-1 level as the 8 hour day length. Dahl et al. (1997)
found a rise in dairy cow plasma IGF-1 after only 4 weeks of exposure
to an 18 hour photoperiod compared to natural photoperiod of less than
13 hours per day. Possibly an effect was not found in our experiment
because the shortest day length that we studied was 14 hours rather
than the 8 hour day used by Spicer et al. (1994) or the natural short
day photoperiod used by Dahl et al. (1997). Day lengths shorter than
14 hours were not examined in the present study as they would not be
representative of a practical indoor dairy barn environment. Our
inability to demonstrate a difference in IGF-1 among our treatment
groups is the strongest evidence we have that day lengths of 14 to 20
hours are all perceived as long days by dairy cows.
When Period 4 was excluded from the data analysis (Table 3) we
found that total milk fat production tended (P = 0.09) to be elevated
for cows exposed to 18 hours of light per day (1.2 Kg d-') compared to
cows exposed to 14 (1.0 Kg d-1) or 16(1.0 Kg d-1) hours of light per
day and results for 20 hours of light per day (1.1 Kg d-1) were
intermediate. The tendency for a rise in milk fat with longer day
length is surprising as others have found no effect of long days
(Phillips and Schofield 1989 - experiment 1 and Dahl et al. 1997) or a
decrease in milk fat (Stanisiewski et al. 1985 and Phillips and
Schofield 1989 - experiment 2) with long days. Our results may relate
to the effect of long days on cow behaviour found by Phillips and
Schofield (1989) where cows exposed to long photoperiod spent 20% more
time lying down. Increased time spent lying would reduce maintenance
cost and thus would make more feed energy available for body fat or
milk fat production.
Conclusions:
There was no evidence in our study for a difference in milk yield,
feed intake or feed efficiency due to day lengths of 14, 16, 18 and 20
hours. However, high levels of variation made it impossible to detect
small or moderate differences.
Total milk fat produced per day tended to be higher for cows
exposed to 18 hours of light per day.
No difference in plasma IGF-1 level was found in cows exposed to
day lengths of 14, 16, 18 and 20 hours.
Overall Conclusions and Implications:
Our results indicate that dairy heifers are not sensitive to 5 or
10 Lux light intensities during the night but respond to 50 Lux for
greater than 2 but less than 4 hours per night. If light with an
intensity of 50 Lux is used at night in dairy barns, cows will receive
less "physiological" hours of darkness than intended, and possibly
needed, for good health. The heifers showed no tendency to develop
either increased or decreased sensitivity to dim light over the course
of the 13 day experimental period. Currently there are dairy
producers who provide light at 50 Lux or higher at night. In such
cases, the presence of light at night may be reducing the length of
night to shorter than that recommended. A recommendation for the use
of 5 or 10 Lux intensity at night in dairy barns would ensure that
light at night does not compromise cow productivity and health.
Milk production and IGF-1 levels were similar for cows exposed to
14 h to 20 h of light per day. Because the variation among treatments
for milk yield was very high, at least a 25% difference among
treatments in milk yield would be required to be significant. At this
point we can only conclude that none of the day length treatments had
a large effect on milk production. A treatment difference may also
have been missed if the treatment duration of 6-weeks was too short in
duration to allow for a full photoperiodic response to develop.
Variation among treatments for plasma IGF-1 level was not excessively
large yet no differences were found among treatments for this hormone
which is thought to mediate the effect of light on milk production.
This is our strongest evidence that day lengths of 14 to 20 hours are
all perceived as long days by dairy cows. When Period 4 was excluded
from the data analysis, we found that total milk fat production tended
to be elevated for cows exposed to 18 hours of light per day compared
to cows exposed to 14 or 16 hours of light per day and results for 20
hours of light per day were intermediate. Our results may relate to
the effect of long days on cow behaviour as it has been shown by
others that cows exposed to long photoperiod spend 20% more time lying
down. Increased time spent lying with a day length of 18 hours would
reduce maintenance cost and thus would make more feed energy available
for body fat or milk fat production.
Acknowledgements:
The authors are grateful to the Agri-Food Research and Development
Initiative (ARDI) and Manitoba Hydro which made it possible to conduct
these studies. Professors K. Plaizier and G. Crow assisted with
experimental planning and statistical analysis. Staff at the Animal
Science Research Unit and Glenlea Dairy Barn provided expert animal
care and assisted with data collection. Eric Witkowski and Ray Boris
of Manitoba Hydro provided technical guidance for both experiments.
Each of the following people made a great effort to ensure that the
experiments were conducted properly and in the process also received
training in the field of animal experimentation. We wish them best
wishes in their future endeavors.
- The M.Sc. student, Pushpa Muthuramalingam, received her degree
at the University of Manitoba spring convocation in 2004. Currently
she is employed as a research associate at a private Winnipeg
molecular biology lab.
- A summer student, Kristen Ficzycz, is currently attending the
Veterinary College in Saskatoon.
- A research assistant, Deanne Fulawka, is currently employed in
the Department of Animal Science.
- Dr. Rob Berry, a research associate who directly supervised this
project, is now the Dairy Specialist for the province of Manitoba.
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