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Comparing simple methods for ageing roe deer Capreolus capreolus: Are any of them useful for management?

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The dynamics of ungulate populations depend not only on the size, but also on the sex- and age-structure of the population. Successful management therefore depends on obtaining estimates of the age composition. Variation in performance due to age can be fairly well described by stages, and simple, rough methods for ageing cervids can therefore be useful to management. We assessed the performance of three relatively simple and objective methods based on tooth wear (height of molar), weight of eye lenses and diameter of pedicles (males only) on a sample of 77 female and 81 male European roe deer Capreolus capreolus from Lier, Norway. The relationship between tooth wear and age was linear, whereas the relationship between weight of eye lenses and diameter of pedicles was curvilinear with age, likely making them unreliable for old age classes. However, as only three males and six females ≥ 6 years old were included, we were unable to assess the uncertainty in age estimation for older age classes precisely. No simple method could precisely age roe deer, even up to five years of age. Our results do suggest that tooth wear, i.e. height of molar, can serve as a very simple and objective measure of age in roe deer, given that moderate precision (an error rate of ± 1 year and a success rate of 70% up to four years of age) is sufficient to reach management aims. As residuals between age estimates based on tooth wear and diameter of pedicle were not correlated, combining these methods improved the fit slightly. Since tooth wear may differ between areas, the scales presented here may perform less well in other areas, and a calibration for each area is clearly recommended.
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SHORT
COMMUNICATION
Comparing simple methods for ageing roe deer Capreolus
capreolus: are any of them useful for management?
Atle Mysterud & Eivind Østbye
Mysterud, A. & Østbye, E. 2006: Comparing simple methods for ageing roe
deer Capreolus capreolus: are any of them useful for management? - Wildl.
Biol. 12: 101-107.
The dynamics of ungulate populations depend not only on the size, but also on
the sex- and age-structure of the population. Successful management therefore
depends on obtaining estimates of the age composition. Variation in perform-
ance due to age can be fairly well described by stages, and simple, rough meth-
ods for ageing cervids can therefore be useful to management. We assessed the
performance of three relatively simple and objective methods based on tooth
wear (height of molar), weight of eye lenses and diameter of pedicles (males
only) on a sample of 77 female and 81 male European roe deer Capreolus capre-
olus from Lier, Norway. The relationship between tooth wear and age was linear,
whereas the relationship between weight of eye lenses and diameter of pedicles
was curvilinear with age, likely making them unreliable for old age classes.
However, as only three males and six females ≥ 6 years old were included, we
were unable to assess the uncertainty in age estimation for older age classes pre-
cisely. No simple method could precisely age roe deer, even up to five years of
age. Our results do suggest that tooth wear, i.e. height of molar, can serve as a
very simple and objective measure of age in roe deer, given that moderate pre-
cision (an error rate of ± 1 year and a success rate of 70% up to four years of
age) is sufficient to reach management aims. As residuals between age esti-
mates based on tooth wear and diameter of pedicle were not correlated, com-
bining these methods improved the fit slightly. Since tooth wear may differ
between areas, the scales presented here may perform less well in other areas,
and a calibration for each area is clearly recommended.
Key words: eye lense weights, pedicle diameter, tooth sectioning, tooth wear
Atle Mysterud, Centre for Ecological and Evolutionary Synthesis (CEES),
Department of Biology, University of Oslo, P.O. Box 1066 Blindern, N-0316
Oslo, Norway - e-mail: atle.mysterud@bio.uio.no
Eivind Østbye, Department of Biology, University of Oslo, P.O. Box 1066
Blindern, N-0316 Oslo, Norway - e-mail: eivind.ostbye@bio.uio.no
Corresponding author: Atle Mysterud
Received 10 September 2004, Accepted 7 November 2004
Associate Editor: Jean-Michel Gaillard
Short communication articles are short scientific entities often dealing with
methodological problems or with byproducts of larger research projects. The
style is the same as in original articles
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102 © WILDLIFE BIOLOGY · 12:1 (2006)
Ungulate populations are strongly structured according
to age and sex (reviews in Tuljapurkar & Caswell 1997,
Gaillard et al. 1998, 2000), so there are large individual
differences in performance within populations that are
related to sex and age. The dynamics of ungulate popu-
lations of similar sizes may subsequently vary accord-
ing to the age and sex composition of the herd (Coulson
et al. 2001). Therefore, a manager needs not only to
obtain indices of abundance or density (as well as oth-
er relevant information regarding condition of the ani-
mals and habitat quality), but preferably also of the sex
and age composition of the population in order to pre-
dict future dynamics, and simple methods to age ani-
mals remain a central challenge in wildlife management.
Fortunately, as performance can be fairly well described
by age stages (i.e. juvenile, subadult, prime-aged and
senescent stages; Gaillard et al. 1998), relatively coarse
methods may be suitable for management.
Tooth sectioning is clearly the most widely used age-
ing method in ungulate research in Scandinavia and
North America, as it has proven a highly reliable age-
ing technique in a number of ungulates inhabiting the
strongly seasonal environments at northern latitudes (see
e.g. Reimers & Nordby (1968) for reindeer Rangifer ta-
randus, Mitchell & Youngson (1969) and Hamlin et al.
(2000) for red deer and elk Cervus elaphus, and Aitken
(1975) for roe deer Capreolus capreolus). Tooth sec-
tioning is based on counting annuli in the tooth cemen-
tum, which arise due to seasonally retarded growth dur-
ing winter and increased growth during summer. How-
ever, to be able to read these lines it is necessary to have
quite sophisticated laboratory equipment, or to send the
samples to laboratories charging ~10€ per individual.
In contrast, alternative methods either utilise the con-
tinuous wear with age (e.g. molar wear; Hewison et al.
1999), growth in the size of the eye lenses (Maringgele
1979, Ashby & Henry 1979, Angibault et al. 1993) or
growth of the pedicles of male antlers (Stubbe et al.
1987, Stubbe 1997). However, the relative performance
of these methods for ageing roe deer is largely unknown.
Further, although the use of tooth wear has been subject
to much research, several studies have assessed tooth wear
based on a subjective scale (Szabik 1973, Hrabe & Kou-
bek 1987, Cederlund et al. 1991). Studies that used an
objective criteria (e.g. height of the molar) differ in their
conclusions, reporting either limited (Cederlund et al.
1991), high (Ashby & Henry 1979) or variable (Hewi-
son et al. 1999) success in predicting age.
In this paper, we compare three fairly simple methods
for ageing roe deer using data on age obtained by tooth
sectioning (as known-age material is unavailable). Our
aim is to determine the success of these methods as
viewed from a management perspective. However, such
methods may also be useful for capture-mark-recapture
studies, because a method for ageing live animals with-
out the extraction of teeth would be valuable (Festa-
Bianchet et al. 2002).
Material and methods
Study area
The study area is located in the Lier valley near Sylling
in the municipality of Lier in the county of Buskerud in
southern Norway (between 59°45'-60°00'N and 10°05'-
10°20'E). Most of the area is forested and situated with-
in the boreonemoral region (Abrahamsen et al. 1977).
Vegetation is varied and dominated by Norway spruce
Picea abies mixed with Scots pine Pinus sylvestris on
the drier and poorer locations. Along the valley bottom
on richer soil, deciduous forest is dominant, fragment-
ed by small, cultivated fields (Kjøstvedt et al. 1998). The
topography is extremely hilly (see Mysterud & Østbye
1995, Mysterud 1999, Mysterud et al. 1999 for a further
description of the study area).
Data
Jaw bones, eye lenses and skulls from 77 female and 81
male roe deer aged ≥ 1 year old were collected and pro-
cessed by Eivind Østbye during 1985-2001. We exclud-
ed fawns, as these can be aged by their pattern of tooth
eruption (only 4-5 cheek teeth in their first autumn;
Cederlund & Liberg 1995). As tooth sectioning is regard-
ed as a highly reliable method for age determination in
strongly seasonal environments such as Norway (for roe
deer, see Aitken 1975), we use 'tooth section age' as
'known age'. The Matson Laboratory in the USA did all
the age determination by tooth sectioning. Any error in
the ageing will most likely increase the error rates report-
ed, and thus if the methods are successful, this would
likely lead to a conservative result. The following three
methods were compared:
Method 1: molar height
Tooth wear is a well-known method frequently used for
ageing cervids including roe deer (e.g. Hewison et al.
1999). We used an objective measure, namely the height
of the second molar (M2) measured to the nearest 0.1
mm using a calibre.
Method 2: eye lens weight
The size of the eye lenses has also been used previous-
ly for ageing roe deer (e.g. Maringgele 1979, Ashby &
Henry 1979). We extracted both eye lenses from fresh
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heads, and used the average weight (to the nearest 0.001
g) after fixation in 10% formalin for 10 days and subse-
quent drying at 80°C.
Method 3: diameter of the pedicles
For males, a method for ageing individuals based on the
diameter of the pedicle has been described (Stubbe et al.
1987, Stubbe 1997). We used average length and width
on both sides of the head as a measure of diameter.
We also tried to combine tooth wear and diameter of
the pedicles (Stubbe et al. 1987, Stubbe 1997).
Statistical analyses
We used linear models to determine the relationship
between our response variables (M2 height, eye lense
weight and pedicle size) and the predictor variables. We
used model selection and assessed fit with the Akaike
Information Criterion (AIC; Johnson & Omland 2004)
or by comparing r2, as the latter was used in previous
studies. We tried adding sex, a sex*age interaction term
and a second-order term for age (in addition to only age).
We also tried an ln-transformation of the response vari-
ables. The most parsimonious model was subsequently
used to derive predictions. We then established intervals
for each age by interpolation from the predicted values
of the best model, and then reclassified the data into age
by using these intervals to check the success rate. All mod-
els were run in S-Plus version 6.2 (Crawley 2003).
Results
Height of the second molar was the only measure lin-
early related to age (Fig. 1A, Table 1). A second-order
term for age entered both the model for the weight of
the eye lenses and for the diameter of the pedicles (see
Table 1). The weight of the eye lenses did not increase
after seven years of age. The diameter of pedicles
seemed not to increase after 4-6 years of age, but this
was only based on two data points, and the relationship
was linear up to five years of age (testing for age2 below
six years of age: T = 0.128, P = 0.898; see Fig. 1). The
weight of the eye lenses was larger for females than for
males. The fit was improved slightly by ln-transform-
ing the height of the molar (r2 = 0.547 vs 0.590), but this
did not apply for the weight of the eye lenses (r2 = 0.713
vs 0.698) or the diameter of the pedicles (r2 = 0.391 vs
0.375). Excluding ages > 7 years decreased the perform-
ance of molar height slightly (r2 = 0.484).
Except for 1-year-old roe deer, no method was able
to determine 50% to the correct age. However, if allow-
ing for ± one year, the success rate of the tooth-wear
method was > 70% up to four years of age, but with a
tendency to overestimate age (Table 2). Similarly, the
success rate 1 year) of the eye-lense method was > 60%
up to five years of age in both sexes, and up to four years
for the size of the pedicle.
It may be possible to combine methods to improve
accuracy in ageing if the same individuals are not over-
or underestimated by both methods, i.e. if the residuals
are not correlated. There was no correlation between
Table 1. Results from model selection and parameter values from the most parsimonious models. Model selection was done starting with
age only, then adding (age)2, sex and sex*age, including or excluding factors depending on whether fit was improved or not. AIC = Akaike
Information Criterion, ΔAIC = difference in AIC value between the AIC for the model given in that row and the most parsimonious model
(lowest AIC), l.s. mean = least square mean, SE = standard error, T = Student’s T test statistic, P = significance probability.
Parameter AIC ΔAIC l.s. mean SE T P
A. ln(molar height)
Intercept 2.1362 0.0135 157.944 0.000
Age -237.151 0.000 -0.0641 0.0046 -13.950 0.000
(Age)2-236.053 1.099
Sex -235.466 1.686
Age*sex -234.097 3.054
B. Eye lense weight
Intercept 0.2184 0.0050 43.914 0.000
Age -681.193 42.292 0.0379 0.0029 12.999 0.000
(Age)2-716.754 6.731 -0.0021 0.0003 -6.890 0.000
Sex -723.485 0.000 -0.0119 0.0040 -2.958 0.004
Age*sex -721.629 1.856
C. Pedicle diameter
Intercept 15.3328 0.7397 20.729 0.000
Age 315.399 2.051 1.9410 0.4918 3.946 0.000
(Age)2313.348 0.000 -0.1255 0.0628 -1.997 0.050
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residuals estimated from tooth wear and those estimated
based on the diameter of the pedicle (rPe = 0.127, df =
66, P = 0.302), very weak correlation between residuals
based on tooth wear and those from size of the eye lenses
(rPe = 0.217, df = 117, P = 0.018), whereas the residuals
from using the size of eye lenses and the diameter of
pedicles to age roe deer were correlated (rPe = 0.522, df =
57, P < 0.001). This indicates that combining methods
using measures of body size will not add much more
predictability, whereas combining tooth wear and meth-
ods using size will improve success. Indeed, slightly
improved precision was obtained when combining tooth
wear with the diameter of the pedicles (see Table 2).
Table 2. Predicted values for the relationship between age and height of the second molar (in mm), weight of the eye lenses (in g) and diameter
of the pedicles (in mm). The intervals used to estimate age in roe deer were based on the most parsimonious models given in Table 1, and
the success rate (proportion correct and proportion within ± 1 year) is given relative to age estimated based on tooth sectioning.
Estimated
age Pre-
dicted Lower
limit Upper
limit
Age - based on tooth sectioning
NProp.
correct Prop.
± 1 year
1 2 3 4 5 6 7 8 9 10 12
A. Molar height 137
1 7.941 >7.695 47 9 3 4 63 0.75 0.89
2 7.448 7.217 7.695 14 9 2 2 27 0.33 0.93
3 6.986 6.769 7.217 4 6 3 3 16 0.19 0.75
4 6.552 6.349 6.769 2 1 7 1 2 1 14 0.07 0.71
5 6.145 5.955 6.349 1 2 1 2 6 0.33 0.50
6 5.764 5.585 5.955 2 2 4
7 5.406 5.238 5.585 1 1 1 3
8 5.070 4.913 5.238 0
9 4.755 4.608 4.913 0
10 4.460 4.322 4.608 1 1 2
11 4.183 4.053 4.322 1 1 2
12 3.924 <4.053 0
B. Eye lense - females 77
1 0.263 <0.277 37 5 42 0.88 1.00
2 0.291 0.277 0.303 2 6 2 1 11 0.55 0.91
3 0.315 0.303 0.325 2 3 3 2 10 0.30 0.80
4 0.335 0.325 0.344 3 2 5 0.40 1.00
5 0.352 0.344 0.359 1 2 1 1 5 0.20 0.80
6 0.366 0.359 0.371 1 1 1 3
≥7 0.376 >0.371 1 1
B. Eye lense - males 81
1 0.251 <0.265 36 5 1 42 0.86 0.98
2 0.278 0.265 0.290 3 4 2 1 10 0.40 0.90
3 0.302 0.290 0.313 1 3 3 3 10 0.30 0.90
4 0.323 0.313 0.331 4 2 3 9 0.22 1.00
5 0.340 0.331 0.347 1 4 1 6 0.00 0.67
6 0.354 0.347 0.359
≥7 0.364 >0.359 1 2 1 4
C. Pedicle diameter 68
1 17.148 <17.931 21 6 2 29 0.72 0.93
2 18.713 17.931 19.370 6 3 2 2 13 0.23 0.85
3 20.026 19.370 20.558 2 2 1 2 1 8 0.13 0.63
4 21.089 20.558 21.495 2 2 2 1 7 0.29 0.86
5 21.900 21.495 22.461 2 1 3 0.00 0.00
≥6 22.461 >22.461 1 4 2 1 8
D. Tooth wear and pedicle diameter 67
1 22 9 1 1 33 0.67 0.94
2 7 1 3 1 12 0.08 0.92
3 2 2 1 2 7 0.14 0.71
4 3 3 3 1 10 0.30 0.90
5 1 1 2 0.50 1.00
≥6 2 1 1 3
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© WILDLIFE BIOLOGY · 12:1 (2006)
Discussion
We compared the performance of three fairly simple
methods for ageing roe deer based on: the relationship
between age and tooth wear, the size of the eye lenses
and the diameter of the pedicles. The main result is that
none of these simple methods could age roe deer pre-
cisely. However, if a lower precision is sufficient, some
of them may still be useful for management.
The general body size in roe deer males reaches a pla-
teau at about 4-5 years of age (Andersen et al. 1998).
Although based on only two data points, we found a pat-
tern consistent with this. From around 4-6 years of age,
the diameter of the pedicles does not seem to increase
further (see Fig. 1). Any size measure will likely per-
form equally well, making this the least useful method.
It is difficult to see any advantages of this method over
for example tooth wear rates.
Size of the eye lenses is a simpler method than tooth
sectioning, and the method performs quite well. Indeed,
for ages up to five years it performs better than tooth
wear (see Table 2). Our results are roughly in accordance
with previous studies also reporting that a plateau for
eye-lense size was reached at about 6-7 years of age (Ma-
ringgele 1979, Ashby & Henry 1979). Ashby & Henry
(1979) concluded that eye lense weights were useless as
a method, since the relationship between age and eye-
lense size was not linear. However, this can be overcome
by fitting a curvilinear relationship for age (see Fig. 1),
and does not mean that the method is useless, but rath-
er that weight intervals for estimating age decrease with
increasing age (see Table 2). The method seems unsuit-
able for age determination above a threshold age of
around seven years. We also found a sex difference in
eye-lense weight, which was not tested for previously.
Sexing the animals can therefore increase performance
relative to previous accounts (Maringgele 1979, Ashby
& Henry 1979). However, drying and preparing the eye
lenses still requires some equipment not available to
most managers, and may therefore be less suited than
tooth wear if larger samples should be processed each
year in population monitoring.
Using either a subjective or objective assessment of
tooth wear has been a common approach to age roe deer
(Szabik 1973, Cederlund et al. 1991, Hewison et al. 1999).
When comparing a subjective assessment of wear with
an objective criteria (height of the molar), Cederlund et
al. (1991) reported that the subjective assessment of wear
seemed to perform slightly better. However, the persons
performing the assessment in Cederlund et al. (1991)
were skilled, possibly underestimating the error rates of
the subjective assessment. A more serious problem is
related to the fact that such subjective methods give biased
results which depend on the experience of the observer,
inexperienced persons typically being more likely to
overestimate age of younger animals and underestimate
age of older animals (Cederlund et al. 1991, Szabik 1973,
Hewison et al. 1999). The studies that have used molar
height to assess age differ in their conclusions, report-
ing either limited (r2 = 0.44; Cederlund et al. 1991), high
(r2 = 0.74; Ashby & Henry 1979) or variable success
Figure 1. Relationship between age (as determined by tooth section-
ing) and A) molar height, B) mean weight of the eye lenses and C)
mean diameter of the pedicles. The lines indicate 95% confidence
intervals.
0 4 10 12
AGE (years)
5
10
15
20
25
DIAMETER OF PEDICLE (mm)
C)
0 8 10 12
AGE (years)
1
3
5
7
9
MOLAR (M2) HEIGHT (mm)
A)
642
0 8 10 12
AGE (years)
0.1
0.2
0.3
0.4
MEAN WEIGHT (g)
Females
Males B)
246
2 6 8
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106 © WILDLIFE BIOLOGY · 12:1 (2006)
depending on population (r2 = 0.36-0.66; Hewison et al.
1999) in predicting age. Our study comes between this
(r2 = 0.59), while two other studies used molar height
without giving an exact fit (Stoddart 1974, Aitken 1975).
In our case, the fit was improved by an ln-transforma-
tion, which was not used in previous studies. Ashby &
Henry (1979) excluded ages of 8-10 years, and indeed,
the wear rate of very old age classes (in red deer) decreased
more than predicted even from a log-linear relationship
(Loe et al. 2003). Our fit was not improved by excluding
the few very old animals, while animals of old age were
not present in the study by Cederlund et al. (1991). At
least some of the within-age variation in tooth wear may
be due to reported individual variation in diet due to
local-scale habitat variation (Mysterud et al. 1999).
Since measuring the height of the molar is an objec-
tive method, it is possible to estimate the likelihood of
bias. Indeed, we seemed to overestimate age with the
tooth-wear method (see Table 2). Also, since error rates
are not much higher than for subjective criteria (Ceder-
lund et al. 1991), this makes it a more appropriate meth-
od for long-term monitoring when changes in the per-
sonnel performing the procedure are common. Some
caution is nevertheless required. Since the performance
of the methods in our study is scaled with the same mate-
rial, as was also done in previous studies (Ashby & Hen-
ry 1979, Cederlund et al. 1991), the intervals presented
may not perform equally well in other areas. Tooth wear
may vary somewhat between areas (Hewison et al.
1999), which may lead to biased estimates. This is not
overcome by using an objective assessment of wear.
Clearly, more sophisticated ways for measuring tooth
wear than molar height may increase precision (Pérez-
Barbería & Gordon 1998a, Pérez-Barbería & Gordon
1998b), but such measures cannot be easily obtained.
As residuals for age estimates based on tooth wear and
those based on the diameter of the size of the pedicle
were not correlated, an increased fit was obtained by
combining the two methods (Stubbe et al. 1987, Stubbe
1997), but this method can only be used with males.
Whether the precision reported for molar height in our
study is good enough or not, depends on the objectives.
For a manager, it is most important to be able to classi-
fy the proportion of juvenile, subadult, adult and senes-
cent stages (see Gaillard et al. 1998). Harvested popu-
lations also have a low average age (Langvatn & Loison
1999), so it may not be important to have a very high pre-
cision for old age classes. Using the height of the molar
provides a very easy method for ageing, and we argue
that it is suitable for most routine studies. However, we
clearly need more information to be able to predict spa-
tially variable molar wear rates in ruminants in general,
which is necessary in order to avoid biased estimates.
Even though these methods are mainly aimed at man-
agement, such methods may also be useful for science
when performing capture-mark-recapture studies, as the
ability to age live animals without having to extract teeth
would be valuable (Festa-Bianchet et al. 2002). This may
be feasible for some species, but error rates will likely be
higher due to measurement error, severely restricting the
applicability in studies of life history variation.
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... age-sex class composition; Gaillard et al. 2000, Williams et al. 2002 of wildlife populations. The mammalian eye lens continues to grow until death (Smith 1883, Krause 1934, Augusteyn 2007a) and hence the dry mass of the eye lens has commonly been used to estimate the age of mammalian species (Lord 1959, Dudzinski and Mykytowycz 1961, Dapson 1980, Mysterud and Østbye 2006, Augusteyn 2007b. The form of the relationship between age and the eye lens mass is similar for all mammal species studied, with an early rapid increase followed by slower increase throughout the life span that approaches an asymptotic maximum (Augusteyn 2008(Augusteyn , 2014. ...
... Knowing age class rather than age may be sufficient for the study and management of many harvested populations (Williams et al. 2002, Mysterud andØstbye 2006). In ungulate populations, the strong age-dependent variation in demographic variables (e.g. ...
... The precision of age predictions obtained using inverse prediction from the Lord model decreased with increasing eye lens dry mass. The increasingly poor precision for heavier eye lenses was due to the curvilinear relationship between age and eye lens dry mass (Dapson 1980, Mysterud andØstbye 2006). However, most estimates of hog deer age will have reasonable precision because few animals  6 years are harvested in southeast Australia ( 12%; Table 1). ...
Article
Full-text available
Estimation of the age or age class of harvested animals is often necessary to interpret the condition and dynamics of wildlife populations. The mammalian eye lens continues to grow until death and hence the dry mass of the eye lens has commonly been used to estimate the age of mammals. The method requires the relationship between eye lens mass and age to be parameterized using individuals of known age. However, predicting age is complicated by the curvilinear relationship between eye lens mass and age. We used frequentist and Bayesian methods to predict the ages and age classes of harvested hog deer Axis porcinus from eye lens mass. Deer were tagged as calves and harvested 4-177 months later in southeastern Australia. Lenses were extracted, fixed and oven-dried. Of the five growth models evaluated, the Lord model best described the relationship between age and eye lens dry mass (R2 = 95%). The precision of age predictions obtained using the Lord model in a Bayesian mode of inference decreased with increasing eye lens dry mass, with the size of the 95% CI equaling or exceeding predicted age for hog deer > 6 years. However, most predictions of hog deer age will have reasonable precision because few animals > 6 years are harvested. Linear discriminant analysis had high predictive power for classifying hog deer to four widely-used age classes (juvenile, yearling, prime-age and senescent). The Bayesian method is recommended for inverse non-linear prediction of age and the frequentist linear discriminant analysis method is recommended for estimating age class. We provide tables of correspondence between hog deer eye lens dry mass and predicted age and age class. Our statistical methods can be used to estimate age and age class for other mammalian species, including from other ageing techniques such as tooth eruption-wear criteria.
... Baltic aspects of roe deer hunt It is very important to estimate the age of roe buck up to five years old (Hewison et al. 1999). The most precise age estimation is possible for an animal up to two years old (Cederlund & Kjellander 1991, Mysterud & Østbye 2006, with a precision of ca. 77 % for animals up to four years (Høye 2006). ...
... 77 % for animals up to four years (Høye 2006). If both tooth wear and pedicle diameter are accounted for, precision is even higher (Mysterud & Østbye 2006). Tooth wear rates are not influ-enced by habitat quality (Veiberg et al. 2007). ...
Article
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With antlers valuated as trophies, ungulates experience high pressures due to selective hunting. The response of the population differs depending on the type of hunting strategy used, and trophies serve as a suitable proxy to answer this question. For example, unrestricted trophy or leisure hunting results in a diminishing quality of trophies. We evaluated the effect of the applied hunting strategy on European roe deer (Capreolus capreolus) antler size in Lithuania, Latvia and Estonia between 2006 and 2011. With the aim of preserving good quality bucks up to 5 years of age, compensatory hunting (culling) is obligatory in Lithuania. To the north, in the other two Baltic countries, roe deer buck are hunted with no age limit. Based on nonparametric tests and forward stepwise discriminant function analysis of antler morphometric characters, Lithuanian roe deer antlers were found to be significantly larger (about 40 % by mean weight and volume for the 35 biggest trophies). We conclude that bucks in Latvia and Estonia are hunted out before they reach trophy maturity (5-7 years). The antlers of fast growing bucks in the age of 3-4 years are almost as big, so they are untimely eliminated from the population. We recommend extending the preservation period of healthy roe deer buck to 6 years of age, giving hunters the possibility to estimate their age not solely on antler size, but also on other body characters.
... There are two key issues when choosing a method of age estimation, (1) bias (the difference between the estimated age and the true age) and precision (the quality of consistently repeating the same estimate), and (2) practicality, defined as how easy or costly it is to apply the method (Morris, 1972(Morris, , 1978Mysterud & Ostbye, 2006). Some methods have low precision, where samples are classified within wide age classes, normally within a few years; these estimates are known as relative age. ...
... loss of elasticity in collagen fibres, tooth wear). These methods can be used in the field, reducing costs and logistics, but at the cost of precision (Brown & Chapman, 1991b;Fandos, Orueta & Aranda, 1993;Pérez-Barbería, 1994;Hewison et al., 1999;HØye, 2006;Mysterud & Ostbye, 2006). ...
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Knowing the age of individuals is crucial for almost any analysis of population dynamics, evolution, palaeontology, management and conservation. The aim of this study was to provide the practitioner with a practical and cost-effective method to estimate the age of large numbers of red deer samples. Using 694 mandibles of Scottish red deer of known age, we compared the bias and precision of five of the most widely used methods for estimating the age of red deer based on tooth characters. Two methods based on reference collections of photographs representing different stages of tooth wear, two methods describing the traits that characterise different classes of the tooth wear and age, and one method based on counting the cementum layers of the radicular pad of the first permanent molar, were used. We also described 13 age classes up to 38 months of age based on different stages of eruption of lower molar teeth. We applied a sequential stepwise-like selection procedure in conjunction with cross-validated predictions using the prediction error sum of squares statistic, with the aim of reducing the large number of traits that the two methods based on tooth wear trait descriptions require to estimate age. We were able to reduce the number of traits by 70% and still gain precision and reduce bias in the predictions, which indicated that the equations provided by these two methods overfitted the age of our reference samples. The cementum layers method was the most precise and least biased of all the methods, followed by Dudley's method. We provide the practitioner with recommendations to allow estimation of the ages of Scottish red deer, together with comprehensive graphic material to facilitate the use of the different methods.
... Tidligere undersøkelser har vist at aldersbestemmelse av voksne rådyr på bakgrunn av tannsnitt gir et bedre estimat på reell alder sammenlignet med andre alternative metoder (Aitken 1975, Ashby & Henry 1979, Mysterud & Østbye. 2006. Presisjonen til metoden har likevel ikke blitt evaluert på samme måte som for elg, hjort og rein . Mangelen på materiale fra dyr med kjent alder er en viktig begrensning for gjennomføringen av en slik undersøkelse. Det er også noe uklarheter hvorvidt tannsnitt av framtenner eller jeksler er det som gir best resultat (Ashby & Henry 1979 ...
Technical Report
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... The ages of the animals were estimated based on tooth wear (both sexes) and the development of antlers in males (41,42). The animals were then assigned to three age groups: (i) fawns younger than 1 year (n = 26), (ii) yearlings and young individuals (n = 26), and (iii) adults older than 3 years (n = 47). ...
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Ashworthius sidemi is an abomasal nematode typical for Asiatic cervids such as sambar (Rusa unicolor) or sika deer (Cervus nippon). This non-native parasite was introduced into Europe via sika deer in the late 19th and early 20th centuries. The current dynamic spread of this parasite amongst autochthonous wild cervids occurs independently of human activities, and A. sidemi has a negative impact on the health of wild ruminants and may pose a threat to the conservation of endangered wild ungulates and to livestock. This invasive parasite has been previously detected in the Czech Republic, but more accurate information on A. sidemi is required. Only limited information is generally available on the factors influencing the spread of abomasal nematodes in wild ruminants, so more information is necessary for planning effective strategies of parasite control. We therefore conducted a survey on the abomasal nematodes in cervids in both game reserves and hunting grounds across the Czech Republic, taking into account the hosts (species, age, sex) and environmental factors (monthly average temperature). The abomasa of 104 animals belonging to five cervid species originating from various locations of the country were collected. Data on host (species, sex, and age group) and the monthly average temperature in the region were obtained for each animal. The parasitological analyses indicated that 92% of the abomasa were infected by nematodes. Ashworthius sidemi was the most prevalent (72%) and abundant (80% of the total recovered individuals) nematode species and was detected in all cervid species except white-tailed deer. The intensity of A. sidemi was highest in roe deer (Capreolus capreolus) and fallow deer (Dama dama), but A. sidemi abundance did not depend substantially on the host or environmental factors. In contrast, the abundance of nematodes from the subfamily Ostertagiinae was influenced by the host species and temperature. Parasitic load was significantly higher in roe deer and during the warmer periods of the survey. We also detected another non-native nematode species, Spiculopteragia houdemeri. The results of our study suggest that the non-native nematode A. sidemi is now widespread amongst cervid hosts in the Czech Republic, probably due to the high sensitivity of autochthonous cervids to A. sidemi infections as well as adaptation of this parasite to the current climatic conditions of this country.
... The large proportion of old deer indicates the importance of adult survival in the maintenance of populations in the semiarid environment of South Texas, where inter-annual variation in recruitment is associated with precipitation patterns. Overall, observers should expect variation in toothwear patterns among individual deer; however, understanding biases for each ageing method can provide support for research and management decisions (Mysterud and Ostbye 2006). ...
Article
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Context The ability to accurately estimate age of animals is important for both research and management. The two methods for age estimation in ungulates are tooth replacement and wear (TRW) and cementum annuli (CA). Errors in estimated TRW ages are commonly attributed to environmental conditions; however, the influence of environmental variables on tooth wear has not been quantified. Further, the performance of CA in environments with weak seasonality has not been thoroughly evaluated. Aims The study had the following three goals: identify environmental and morphological factors that influenced estimated ages, quantify accuracy of TRW and CA, and develop TRW ageing criteria that minimise error. Methods We used data from harvested (n = 5117) and free-ranging, known-age white-tailed deer (n = 134) collected in southern Texas, USA, to quantify environmental and morphological influences on estimated TRW ages, and assess biases in both methods. Key results We observed substantial variation in age estimates for both TRW and CA. Soil, drought and supplemental nutrition had minor effects on tooth wear, insufficient to alter age estimates by ≥1 year. Body mass and antler size influenced age estimates for TRW only for extreme outliers. Both methods were biased and tended to under-estimate ages of adult deer, especially TRW. Wear on the first molar was most correlated with the known age (r² = 0.78) and allowed biologists to correctly place known-age deer into age classes of 2, 3–5, and ≥6 years old 72%, 73% and 68% of the time, an improvement compared with the 79%, 48% and 28% accuracy from pooled TRW. Conclusions We observed substantial inter- and intra-individual variation in tooth-wear patterns that became more pronounced in older deer. Individual variation had a greater influence on TRW ages than did environmental covariates, whereas CA ages appeared unaffected by environment. Although variable, age estimates were ±1 year of the true age 87% and 93% of the time for TRW and CA respectively. Implications Managers, ecologists and epidemiologists often incorporate ages into population models. The high inter-individual variation in estimated ages, the tendency to underestimate ages of older deer, and the ageing method need to be considered.
... Age estimation of free living game animals and proper division in age groups is critical for understanding population dynamics and development of management strategies. Very precise methods are used to determine age in dead animal: antler beam diameter, tooth wear and replacement, molar tooth ratio, eye lens weight (mysterud and Østbye, 2006, Stubbe, 1997, Ueckermann and Scholz 1976, Almasan and rieck, 1970, Andersen, 1953. Age estimation in live roe deer can be enduring, since there is no reliable visible characteristic (Strandgaard, 1972). ...
Article
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Population of roe deer (Capreolus capreolus) living in the selected hunting estates in the Eastern Croatia has been studied. Specimens were collected at locations in hunting estates: Osijek, Podunavlje, Spačva and Kunjevci, which differs in habitat composition and characteristics of roe deer's populations. Aim of the study was to determine the most applicable parameter among size of the body parts for classification of live individuals into age groups. Total of 161 individuals was measured. The most pronounced body measures: head length and body length have linear increase in relation to age. Continuous growth throughout age classes was significant for the head length and for the body length. The lowest values of measured parameters were confirmed for Podunavlje and Kunjevci, the significantly higher values were in Osijek, while the values were intermediate in Spačva. Based on the results, a recommendation for the age estimation in live roe deer is to observe head length and eye position in relation to snout.
... , VAN DEELEN et al. 2000, GEE et al. 2002 V praksi se zbrane čeljustnice najpogosteje (marsikje rutinsko, čeprav pogosto ne dovolj kritično) uporabljajo za ocenjevanje starosti živali (npr. HRABE / KOUBEK 1987, HEWISON et al. 1999, AZORIT et al. 2004, MYSTERUD / ØSTBYE 2006, HØYE 2006, KAISER et al. 2009). Z makroskopskim (okularnim) pregledom čeljustnic in zob (predmeljakov -p/P, meljakov -m/M, pri divjem prašiču in muflonu tudi sekalcev -i/I) je mogoče za osebke večine vrst parkljarjev do dokončane menjave mlečnih zob v stalne starost živali ugotoviti skoraj do meseca natančno. ...
Article
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To check the reliability of macroscopic (ocular) assessment of the age of red deer (Cervus elaphus L.) obtained by ocular inspection of teeth eruption and wear (done by hunters or hunter commissions), a validation of the precision of these assessments was carried out on a representative sample set, i.e. a total 2008-annual cull of red deer in the entire Slovenia. Test of the reliability of ocular age assessment was performed by cutting/grinding of the first mandibular molar (M1) and counting the incremental layers of dental cementum on 821 samples of adults (aged from two to twenty-two years). The ocular age assessment of adult red deer (regardless of sex) was biased with a large error (maximum deviation between both assessments: nine years). With both methods the same animal age was established in 24.5% of cases, and with the age of the animals the reliability of ocular assessment declined. Ages of hinds and younger stags were both under-assessed and over-assessed; however, ages of older stags were generally over-assessed. Out of 426 analysed stags, 142 (33.3%) were categorized in another age category as found by counting annuli in tooth cementum. This raises doubts about the reliability of the current categorization of adult red deer stags into three age categories (2–4 years old, 5–9 years old, and 10+ years old, respectively); indeed, precise (on a yearly basis) ages of adult stags are impossible to be identified by routine age assessment, such as the inspection of teeth wear.
... We also excluded counties 4, 6, 9, 15 and 16 ( Fig. 1) and the years 1987 and 1988 from both data sets, and also 1989 from the prime stag data set because of low harvesting numbers, leaving a total of 126 017 individuals available for analyses. Age was estimated by tooth wear (Szidnai 1978), a method known to show some variation for older individuals (Mysterud & Østbye 2006) but also variation between (Veiberg et al. 2007) and within populations (Nussey et al. 2007). As the same method was utilized over the full data set, it is unlikely that over-or underestimation of age plays a role for the observed patterns, but we are aware that the ageing method probably adds some noise to the data, particularly for older individuals. ...
Conference Paper
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Article
Length and structural complexity of antlers provide an indication of individual quality in many ungulates in the context of female mate choice and trophy hunting. Selectivity of hunters for individuals with various antler sizes may have bearing on the population structure. It is less well understood, however, whether and how antler anomalies may signal individual characteristics. We used data on 2,461 roe deer (Capreolus capreolus) males harvested by stalking during 1966–2011 in western Poland to test hypotheses explaining probability of occurrence of accessory, broken, and malformed antlers. By employing a multinomial logistic regression, we showed that the probability of occurrence of broken and malformed antlers increased in males older than 2 years. Probability of occurrence of accessory and, in young males, broken antlers was higher in individuals with increased body weight. Occurrence of malformed antlers decreased over the study period. Contrary to our prediction, we did not detect an effect of distance to forest on the probability of malformed antlers occurring. We conclude that the main premise of compensatory culling is not supported in roe deer. © 2014 The Wildlife Society.
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In large-herbivore populations, environmental variation and density dependence co-occur and have similar effects on various fitness components. Our review aims to quantify the temporal variability of fitness components and examine how that variability affects changes in population growth rates. Regardless of the source of variation, adult female survival shows little year-to-year variation [coefficient of variation (CV<10%)], fecundity of prime-aged females and yearling survival rates show moderate year-to-year variation (CV<20%), and juvenile survival and fecundity of young females show strong variation (CV>30%). Old females show senescence in both survival and reproduction. These patterns of variation are independent of differences in body mass, taxonomic group, and ecological conditions. Differences in levels of maternal care may fine-tune the temporal variation of early survival. The immature stage, despite a low relative impact on population growth rate compared with the adult stage, may be the critical component of population dynamics of large herbivores. Observed differences in temporal variation may be more important than estimated relative sensitivity or elasticity in determining the relative demographic impact of various fitness components.
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Spośrod 1506 zuchw rogaczy sarn, Capreolus capreolus (Linnaeus, 1758) odstrzelonych w poludniowo-wschodniej Polsce w latach 1969-1971 wybrano 200 (Tabela 1) reprezentujących cztery rozne siedliska (Fig. 1). Wiek tych rogaczy określono najpierw na podstawie starcia zebow, a potem bezwzglednie, wedlug liczby sloi zimowych w cemencie I1 (Fig. 2).
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A rapid freeze-sectioning technique for demonstrating annuli in tooth cementum of reindeer (Rangifer tarandus) is described. The technique has been applied to a reference material of 37 adult known-age animals and to 1,100 jawbones from two reindeer populations. The known-age material strongly indicates that the annulation is referable to age. The presence of special rut lines in teeth of males from high quality range indicates that rut-line formation might be related to condition.
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