2007 NORTHEASTERN NATURALIST 14(3):375–386
The Timing of Waterfowl Arrival and Dispersion During
Spring Migration in Labrador
Keith G. Chaulk1,* and Bruce Turner2
Abstract - Weekly aerial surveys were conducted in central Labrador during the spring
staging period (27 April to 29 May, 2000), and the relative abundance of waterfowl
was documented. Anas rupribes (American Black Duck) and Bucephala clangula
(Common Goldeneye) were among the first species to arrive, while peak waterfowl
diversity occurred on the latest survey date. Overall, Branta canadensis (Canada
Geese) were the most abundant species, followed by American Black Duck and Anas
crecca (Green-winged Teal). As expected, the relative abundance of these species
varied by date and region. By the time of the last survey on 29 May, average flock size
had decreased for most species, most likely corresponding with the start of breeding
and nest initiation. Our findings could be useful as baseline information for future
studies of climate change, may have implications for the management of the aboriginal
spring hunt, and also might be used to mitigate the effects of military flying activity.
Introduction
Understanding spatial and temporal patterns in the distribution and abundance
of animals is important because these patterns can be indicators of
ecosystem change. Migratory birds in the high latitudes are particularly
interesting in this respect because of the apparent regularity and extent of
their annual movements (Gwinner 1996). Many migratory bird species start
their migration on or around the same time each year (Coppack and Both
2002). However, recent evidence has demonstrated that large-scale processes
like climate change can influence the timing of migration (Coppack
and Both 2002, Hüppop and Hüppop 2003) and breeding (Both and Visser
2001, Brown et al. 1999, Crick and Sparks 1999, Crick et al. 1997).
While many waterfowl demonstrate fidelity to breeding sites (Eadie and
Gauthier 1985, Seymour 1991, Zicus and Hennes 1989), or wintering sites
(Hestbeck et al. 1991, Lincoln 1934), and in some cases to staging areas
(Afton and Hier 1987), it is not clear if all species demonstrate fidelity to
staging areas (Moison et al. 1967). Regardless, spring migration is an
important period during waterfowl life history, and staging areas provide
waterfowl with the resources needed to maintain, restore, or increase the
energy reserves to meet the demands of migration and reproduction. Different
strategies are evident across different species (Alisauskas and
Ankney 1992, Gauthier et al. 1984, Krapu and Rienecke 1992, McLandress
and Ravelling 1981, Thomas 1982). In this paper, we look at temporal and
spatial patterns of waterfowl on staging habitats during the spring period in
1Canadian Wildlife Service, Goose Bay, NL, A0P 1C0, Canada. 2Canadian Wildlife Service,
Mt. Pearl, NL, A1N 4T3, Canada. *Corresponding author - keith.chaulk@ec.gc.ca.
376 Northeastern Naturalist Vol. 14, No. 3
Labrador, a sub-arctic region in eastern Canada. This information may
have use for future population-monitoring surveys, and/or comparing the
effects of climate change on waterfowl migration patterns in this sub-arctic
region. Our findings may have implications for the management of the
aboriginal spring hunt, and also be might be used to mitigate the effects of
military flying activities in Labrador.
Study Area
The study area was divided into three general regions centered on
Goose Bay, NL (Fig. 1). The southern region contained survey sites with
Figure 1. Study area of spring-staging surveys conducted in Labrador from 27 April
to 29 May 2000. Map shows the location of the three general survey regions
(northern, central, and southern).
2007 K.G. Chaulk and B. Turner 377
the highest altitudes, with elevation up to 350 m above sea level (asl)
followed by the northern and central regions, with elevation as low as 2 m
asl. The study area is typically described as sub-arctic, comprised of boreal
forest, taiga, tundra, wetlands, lakes, river systems, and mountainous terrain.
The frost-free period ranges from 40 days in the north to 100 days in
the south (Department of National Defence 1994)
Methods
Survey methods
Fourteen water systems were surveyed in helicopter over a 5-week
period in the spring of 2000; these systems were grouped into three broad
geographic sub-regions (north, central, and south). Each water system was
visited once per week, and in total, 5 surveys were flown. Surveys were
based out of Goose Bay, NL, and the weekly surveys were conducted from
27 April to 29 May, 2000. It should be noted that the labels north, central,
and south are relative to this study, in that all survey sub-regions are
located in Southern and Central Labrador, with the majority of sites located
within Central Labrador.
Surveys were conducted using an Enstrom EN-480 helicopter. Typical
cruising speed was 110 km/h, but on-site survey speed ranged from 30–60
km/h, and on-site aboveground altitudes ranged from 15–30 m. Crew size
varied from 2–3 people, but the pilot and primary researcher held constant
for all surveys. Field observations, such as snow cover and species
type and abundance, were collected using a laptop connected to a
hand-held GPS unit and microphone. The GPS unit was mounted inside
the aircraft with an unobstructed view of the sky. Geodetic coordinates
were recorded in latitiude/longitude decimal degrees North American
Datum 1983.
The laptop was running the US Fish and Wildlife Service GPS Voice
Survey Recording Program (v 3.1). The program was divided into 2 subprograms
(record and transcribe). The record portion was used to collect
field information and data-log flight-track information. By clicking the
mouse pad, geodetic coordinates were linked to individual observations,
stored in the form of audio files. The transcribe portion of the program was
used to process the audio files and turn them into alpha numeric text (i.e.,
names and numbers). The post-processed data could then be exported to
various software programs for mapping and data analysis. Post-processed
data was saved as a database and stored in File Maker Pro (v 4.0), mapping
was conducted in MapInfo (v 4.5), and statistical analyses and graphing
were performed using Minitab (v 14.2).
Sites were selected for observation based on a combination of previously
identified spring staging habitats (Bateman et al. 1999), satellite imagery,
and aboriginal environmental knowledge provided by Innu elders. In general,
the water systems investigated in this study were those areas of first
378 Northeastern Naturalist Vol. 14, No. 3
open water in the spring and were selected due to their known or predicted
importance to waterfowl spring staging, as they provide secure roosting sites
and access to foraging habitat in an otherwise frozen landscape. Average
snow cover was visually estimated for each site and compiled for each
region. Waterfowl that were not positively identified were classed as one of
the following: unidentified duck, unidentified diver, unidentified dabbler, or
unidentified merganser/goldeneye, depending on the level of uncertainty
of the observer. No effort was made to correct for potential auto-correlation
of observations between survey weeks or regions. Sceintific names with
authorities are given in Table 1 and species names are based on accounts
from the Birds of North America.
We used abundance and flock size to index the timing of waterfowl
arrival and dispersion. Abundance and flock size are both expected to be
highest in early spring periods when limited open water causes waterfowl
to congregate. As many of these first open-water areas are not preferred
breeding habitats, abundance and flock size are expected to decrease as
spring progresses and waterfowl disperse to more favourable breeding
and foraging habitats.
Statistics
We developed two separate general linear models with abundance as the
response variable. Predictors in model 1 included: species, survey region,
and their interaction. Predictors in model 2 included: species, survey week,
Table 1. Summary of species and individuals for all regions all surveys. Observation made
during weekly aerial surveys conducted in central Labrador from 27 April to 29 May, 2000.
Total Total
individuals # of flocks Average
Scientific name Common name counted observed flock size
Branta canadensis (L.) Canada Goose 6882 572 12.0 ± 1.2
Anas rupribes (Brewster) Black Duck 1252 356 3.5 ± 0.2
Anas crecca (L.) Green-winged Teal 934 117 8.0 ± 1.2
Bucephala clangula (L.) Common Goldeneye 906 270 3.4 ± 0.2
Aythya marila (L.) Greater Scaup 841 147 5.7 ± 0.8
Unknown duck 631 74 8.5 ± 1.7
Melanitta perspicilatta (L.) Surf Scoter 609 105 5.8 ± 0.7
Mergus spp. Unknown merganser 543 149 3.6 ± 0.5
Mergus merganser (L.) Common Merganser 211 61 3.5 ± 0.7
Anas acuta (L.) Northern Pintail 94 37 2.5 ± 0.3
Anas clypeata (L.) Northern Shoveler 71 18 3.9 ± 0.6
Anas platyrhynchos (L.) Mallard 57 24 2.4 ± 0.4
Unknown merg/gold 55 13 4.2 ± 0.5
Histronicus histronicus (L.) Harlequin Duck 45 16 2.8 ± 0.4
Aythya collaris (Donovan) Ringed-neck Duck 43 17 2.5 ± 0.3
Unknown diver 33 17 1.9 ± 0.2
Mergus serrator (L.) Red Breasted Merganser 22 11 2.0 ± 0.4
Melanitta nigra (L.) Black Scoter 21 6 3.5 ± 1.0
Melanitta fusca (L.) White Winged Scoter 7 2 3.5 ± 1.5
Anas Americana (Gmelin) American Wigeon 3 2 1.5 ± 0.5
2007 K.G. Chaulk and B. Turner 379
and their interaction. Unfortunately, due to rank deficiency resulting from
limited sample size, we were precluded from using the model: species,
survey week, survey region, and their interactions.
Results
Seasonal phenology
Mean monthly temperatures for Goose Bay, the only reporting station
within the study area, were above normal in April (observed = -0.3 oC;
average = -1.8 oC) but below normal in May (observed = 4.3 oC ; average =
5.1 oC). Total precipitation was above normal in both April (observed 70.0
mm; average 57.1 mm) and May (observed = 101.0 mm; average = 66.4
mm). The study area was 99% snow-covered at the start of the survey period,
decreasing to 0% for some sites by the end of the survey period. Spring melt
did not occur uniformly, being faster at lower elevations in the central region
and slower at higher elevations in the southern and northern regions.
In all areas, at the time of the first survey (27 April), the ground was
completely snow-covered, all lakes and streams were frozen, and open water
was confined to only a few water systems in the southern region. Between 7
May and 15 May, the spring thaw was delayed by below-normal temperatures
and above-normal precipitation, which fell as snow. Temperatures
warmed during the third week, and extensive melting occurred by the last
week of May (Fig. 2).
Figure 2. Average percent snow-cover (95% CI), summarized by week and survey
region. Snow-cover information based on repeated visual observations at 27
survey sites in the study area (one recording per site/per survey week). These 27 sites
were pooled by survey sub-region (south, central, north). Observation made during
weekly aerial surveys conducted in central Labrador from 27 April to 29 May, 2000.
380 Northeastern Naturalist Vol. 14, No. 3
Figure 3. Relative abundance by survey region for 6 species of waterfowl. Observations
made during weekly aerial surveys conducted in Labrador from 27 April to 29
May, 2000. Note that the Y axes change by species.
Overall diversity and abundance
Over 13,000 individual waterfowl were counted between 27 April–29
May, 2000. In order, the five most abundant waterfowl were: Canada Goose,
American Black Duck, Green-winged Teal, Common Goldeneye, and
Greater Scaup (Table 1). Of observed waterfowl species, the 3 least abundant
species were Black Scoter, White-winged Scoter, and American
Wigeon, and overall, fifteen species of waterfowl were positively identified
(Table 1). The northern region had the highest diversity (15 species), while
the southern region had the lowest overall waterfowl diversity (11 species).
The lowest waterfowl diversity was observed on the earliest survey date (27
April; 4 species), the greatest waterfowl diversity occurred on the latest
survey date (29 May; 15 species).
Spatial patterns
We found that species and region had a significant interaction
(P < 0.01, DF = 299, F = 1.88, R2 = 42.85%). Overall, the northern survey
region had the highest counts for Canada Goose, Greater Scaup, and
Common Goldeneye, the central survey region had the highest counts for
Green-winged Teal and Black Duck, while Surf Scoters were equally
abundant in the southern and northern regions (Fig. 3).
Temporal patterns
We found that species and week had a significant interaction (P < 0.01,
DF = 299, F = 3.34, R2 = 62.15). Overall, Canada Goose abundance was
2007 K.G. Chaulk and B. Turner 381
highest on 7 May, while Green-winged Teal and Greater Scaup abundance
peaked on 22 May. American Black Duck and Common Goldeneye abundance
were greatest on 15 May, while Surf Scoters were late in arriving and
were equally abundant on 22 and 29 May (Fig. 4).
Average flock size varied by survey week depending on the species in
question. Green-winged Teal flock sizes were relatively constant across
survey dates (Fig. 5). Average flock size for Greater Scaup and Surf Scoter
were lowest from 27 April to 7 May, and average flock sizes for Surf
Scoter continued to increase as the survey period progressed, suggesting
later nesting (Fig. 5). With respect to Canada Goose, American Black Duck,
and Common Goldeneye, the largest average flock sizes were observed on 7
May, with flock sizes of these 3 species declining thereafter, most likely
coinciding with the dispersal to breeding habitats (Fig. 5). The first active
goose nests were observed in the central region on 29 May.
Discussion
With the exception of Canada Geese (Mowbray et al. 2002), the study
area is near the range edge for many of the species observed including,
American Black Duck, Green-winged Teal, Common Goldeneye, Surf
Scoter, and Greater Scaup. The timing and extent of spring migration
varies slightly for each species (Eadie et al. 1995, Johnson 1995, Kessel
et al. 2002, Longcore et al. 2000, Savard et al. 1998). Unfortunately, very
Figure 4. Relative abundance by survey week for 6 species of waterfowl. Observation
made during weekly aerial surveys conducted in Labrador from 27 April to 29
May, 2000. Note that the Y axes change by species.
382 Northeastern Naturalist Vol. 14, No. 3
Figure 5. Average flock size summarized by week for 6 species of waterfowl. Observations
made during weekly aerial surveys conducted in central Labrador from 27 April to
29 May, 2000. Dashed lines represent overall average flock size by species. Note that
the Y axes change by species. The reader should note that the minimum error bar value
for Green-winged Teal (date = 5/7) is negative and has not been truncated.
few published reports exist with respect to the timing of spring migration
in this sub-arctic region, so there is a paucity of information with respect
to waterfowl staging during the spring period in Labrador.
We found that the abundance of each species had a significant interaction
with survey region, probably reflecting variable habitat conditions across
regions. For example, latitude, elevation, vegetation, and wetlands could all
play important roles influencing abundance patterns, with each species responding
differently. Overall, the northern survey region was most
productive for Canada Goose, Greater Scaup, and Common Goldeneye,
while the central survey region was most productive for Green-winged Teal
and American Black Duck; the southern and northern regions were equally
productive for Surf Scoter. We also found that species abundance and survey
week had a significant interaction; this was expected since each species has
slightly different timing with respect to migration and consequently for the
start of breeding and nesting.
As the surveys were conducted during a single season, the findings
should be considered more indicative than representative of temporal aspects
of arrival and dispersal of waterfowl using spring staging habitats in
Labrador. Additional surveys across several years are required to clearly
establish annual variation. It should be noted that the timing of migration
and subsequent nest initiation in more northerly areas of Labrador (>55o N)
2007 K.G. Chaulk and B. Turner 383
could be delayed by 1–3 weeks relative to our study areas, depending on the
progress of spring. Unfortunately, we have limited information on which to
make a generalized statement, but we do know that Somateria mollisima
(L.)(Common Eiders) breeding in northern Labrador have average nestinitiation
dates that can be 2–3 weeks later than Common Eiders nesting in
more southern and central regions of Labrador (Chaulk et al. 2004).
From late April to mid-May, we found that the amount of open-water
habitat was quite limited, being restricted to fast-flowing rivers, river
inlets and outlets, constrictions in lakes, and in the littoral areas of the
tide-influenced central region. Snow cover appeared to vary with date,
latitude, altitude, forest canopy cover, and presence of water (i.e., river,
lake, wetland). Fast-moving rivers and drainage areas were the first to
open, followed by lakes and wetlands; forested areas were the last
to thaw. It should be noted that the study area was subjected to snow
storms during the month of May, which resulted in increased snow cover
for some areas as the spring progressed.
The total numbers of observed waterfowl comprise but a small percentage
of the total waterfowl estimated to breed in Labrador. Nonetheless, the results
provide a basis on which to assess the timing and duration of spring migration
for these six species. While total waterfowl numbers in each of the three regions
(south, central, and north) followed a general pattern of increase to 7 May, and
decreases after 22 May, species exhibited differences. For example, by 29 May,
Surf Scoters were still increasing, while Canada Geese had largely dispersed
from staging habitats.
During Black Duck surveys in the 1990s (Bateman and Hicks 1999),
Canada Goose goslings were observed as early as 29 May in the central
survey region (K. Chaulk, pers. observ.), indicating nest initiation in late
April. During our study, we did not observe any goslings, and the first active
goose nest was not detected in the central region until 29 May 2000.
However,with few exceptions (Chaulk et al. 2004, 2005), very little is
published with respect to average nest-initiation dates for any waterfowl
species in Labrador. Nonetheless, it appeared that the spring period in May
2000 was later arriving than normal, and it seems likely that goose nesting
was delayed as a result. Of those species reported, Surf Scoter flock and
overall abundance were still increasing at the end of the survey period,
suggesting that this species has much later nesting than the other species,
most likely starting in June (Savard and Lamothe 1991).
Labrador is an important breeding area for many waterfowl populations
of the Atlantic flyway, and our results may be of interest to regional researchers
and managers. Our results could also serve as baseline information
for studies investigating impacts of climate change on the timing of waterfowl
migration, and might have application with respect to establishing
spring hunting seasons for aboriginal people living in central Labrador. For
example, the Labrador Inuit have finalized their land-claim process, which
384 Northeastern Naturalist Vol. 14, No. 3
provides waterfowl-harvesting rights during the spring period (LIA 2005).
In the past, closing dates for the spring hunt have been based on traditional
Inuit knowledge regarding the timing of transition from migration to nesting.
The information presented here corresponds well with Inuit Knowledge,
and may be useful in the co-management of the spring hunt in Nunatsiavut
and surrounding areas. In addition, the information presented here may also
be used to mitigate impacts of the Department of National Defence military
flying program that operates out of Goose Bay, NL.
Acknowledgments
We acknowledge the Innu Nation for providing important aboriginal ecological
knowledge with respect to waterfowl spring staging. This project was made possible
with funding from the Department of National Defence, and from the Canadian
Wildlife Service.
Literature Cited
Alisauskas, R.T., and C.D. Ankney. 1992. The cost of egg laying and its relationship
to nutrient reserves in waterfowl. Pp. 30–61, In Bruce D.J. Batt, Alan D.
Afton, Michael G. Anderson, C. Davison Ankney, Douglas H. Johnson, John A.
Kadlec, and Gary L. Krapu. (Eds.). Ecology and Management of Breeding
Waterfowl. University of Minnesota Press, Minneapolis, MN.
Afton, A.D., and R.H. Hier. 1987. Recovery rates and distribution of color-marked
Lesser Scaup staging in Northwestern Minnesota. Minnesota Department of
Natural Resources, Minneapolis, Minnesota. Unpublished Report.
Bateman, M.C., and A.H. Hicks. 1999. Waterfowl populations in Labrador: A data
compilation and analysis. Canadian Wildlife Service Report, Sackville, NB,
Canada.
Both, C., and M.E. Visser. 2001. Adjustment to climate change is constrained by
arrival date in a long-distance migrant bird. Nature 411:296–298.
Brown, J.L., S.H. Li, and N. Bhagabati. 1999. Long-term trend toward earlier
breeding in an American bird: A response to global warming? Proceedings of
the National Academy of Science. USA 96:5565–5569.
Chaulk, K.G., G.J. Robertson, and W.A. Montevecchi. 2004. Regional and annual
variability in Common Eider nesting ecology in Labrador. Polar Research.
23:121–130.
Chaulk, K.G., G.J. Robertson, W.A. Montevecchi, and P. Ryan. 2005. Aspects of
Common Eider breeding ecology in Labrador. Arctic 58:10–15.
Coppack T., and C. Both. 2002. Predicting life-cycle adaption of migratory birds to
global climate change. Ardea 90:369–378.
Crick, H.Q.P., and T.H. Sparks. 1999. Climate change related to egg-laying trends.
Nature 399:423–424
Crick, H.Q.P., C. Dudley, D.E Glue, and D. Thomson. 1997. UK birds are laying
eggs earlier. Nature 388:526.
Department of National Defence (DND). 1994. Military flight training: An
envvironmental impact statment on military flight training in Labrador and
Quebec. Project Management office Goose Bay, National Defence
Headquarteers, Ottawa, Ontario.
2007 K.G. Chaulk and B. Turner 385
Eadie, J.M., and G. Gauthier. 1985. Prospecting for nest sites by cavity-nesting
ducks of the genus Bucephala. Condor 87:528–534.
Eadie, J.M., M.L. Mallory, and H.G. Lumsden. 1995. Common Goldeneye
(Bucephala clangula). In A. Poole and F. Gill (Eds.). The Birds of North
America, No. 170. The Academy of Natural Sciences, Philadelphia, and the
American Ornithologists’ Union, Washington, DC.
Gauthier, G., J. Bédard, J. Huot, and Y. Bédard. 1984. Spring accumulation of fat
by Greater Snow Geese in two staging habitats. Condor 86:192–199.
Gwinner, E. 1996. Circannual clocks in avian reproduction and migration. Ibis
138:47–63.
Hestbeck, J.B., J.D. Nichols, and R.A. Malecki. 1991. Estimates of movement and
fidelity using using mark-resight data of wintering Canada Geese. Ecology
72:523–533
Hüppop, O., and K. Hüppop. 2003. North Atlantic Oscillation and timing of
spring migration in birds. Proceedings of the Royal Society of London. B
270:233–240.
Johnson, K. 1995. Green-winged Teal (Anas crecca). In A. Poole and F. Gill (Eds.).
The Birds of North America, No. 170. The Academy of Natural Sciences,
Philadelphia, and the American Ornithologists’ Union, Washington, DC.
Kessel, B.D., D.A. Rocque, and J.S. Barclay. 2002. Greater Scaup (Aythya marila).
In A. Poole and F. Gill (Eds.). The Birds of North America, No. 650. The Birds
of North America, Inc. Philadelphia, PA.
Krapu , G.L and K.J. Rienecke. 1992. Foraging ecology and nutrition. 1–29 pp., In
B.D.J. Batt et al. . Bruce D.J. Batt, Alan D. Afton, Michael G. Anderson, C.
Davison Ankney, Douglas H. Johnson, John A. Kadlec, and Gary L. Krapu.
(Eds.). Ecology and Management of Breeding Waterfowl. University of Minnesota
Press, Minneapolis, MN.
Lincoln, F.C. 1934. The operation of homing instinct. Bird Banding 5:149–155.
Longcore, J.R., D.G. McAuley, G.R. Hepp, and J.M. Rhymer. 2000. American
Black Duck (Anas rubripes). In A. Poole and F. Gill (Eds.). The Birds of North
America, No. 170. The Academy of Natural Sciences, Philadelphia, and the
American Ornithologists’ Union, Washington, DC.
Labrador Inuit Association (LIA). 2005. Labrador Inuit Land Claims Agreement.
Bill C-56. Ottawa, ON, Canada.
McLandress, M.R., and D.G. Raveling. 1981. Changes in diet and body composition
of Canada Geese before spring migration. Auk 90:65–79.
Moison, G., R.I., Smith, and K. Martinson. 1967. The Green-winged Teal: Its
distribution, migration, and population dynamics. US Fish and Wildlife Service,
Washington, DC. Species Science Report Wildlife 100.
Mowbray, T.B., C.R. Ely, J.S. Sedinger, and R.E. Trost. 2002. Canada Goose
(Branta canadensis.) In A. Poole and F. Gill (Eds.). The Birds of North
America, No. 682. The Birds of North America, Inc., Philadelphia, PA.
Savard, J.P-L., and P. Lamothe. 1991. Distribution, abundance, and aspects of
breeding ecology of Black Scoters (Melanitta nigra) and Surf Scoters (M.
perspicillata) in Northern Quebec. Canadian Field-Naturalist. 105:488–496.
386 Northeastern Naturalist Vol. 14, No. 3
Savard, J.P.L., D. Bordage, and A. Reed. 1998. Surf Scoter (Melanitta perspicillata).
In A. Poole and F. Gill (Eds.). The Birds of North America, No. 170. The
Academy of Natural Sciences, Philadelphia, and the American Ornithologists’
Union, Washington, DC.
Seymour. N.R. 1991. Philopatry in male and female American Black Ducks. Condor
93:189–191.
Thomas, V.G. 1982. Spring migration: The prelude to goose reproduction and a
review of its implications. In H. Boyd (Ed.). Proceedings of the International
Waterfowl Research Bureau Symposium. Canadian Wildlife Service, Ottawa
ON, Canada. Special Publication.
Zicus, M.C., and S.K. Hennes. 1989. Nest prospecting by Common Goldeneyes.
Condor 91:807–812.