EFFECTS OF NECK BANDS ON CANADA GEESE. NESTING AT THE McCONNELL RIVER CHARLES D. MAGINNES AND ERIGA H. DUNN

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J. Field Ornithol., 59(3):239-246 EFFECTS OF NECK BANDS ON CANADA GEESE NESTING AT THE McCONNELL RIVER CHARLES D. MAGINNES AND ERIGA H. DUNN Ministry of Natural Resources Wildlife Research Section P.O. Box 50 Maple, Ontario LOJ leo, Canada Abstract.--Canada Geese (Branta canadensis) neck-banded at McConnell River, Northwest Territories were recaptured on the nesting grounds less frequently than geese leg-banded at the same locality. The difference could result from increased mortality, or emigration of neck-banded geese to nest elsewhere. Our data cannot distinguish between these causes, because other factors confounded the analysis. Hunters recovered the same proportions of neck-banded and leg-banded geese despite the fact that fewer neck-banded geese were recaptured. That could result from enhanced reporting due to neck bands, or hunter selection for visibly marked geese. There were no consistent detrimental effects on reproductive performance of neck-banded geese. Assessment of effects of neck bands should be included in the design of any study that uses such bands. EFECTOS DE BANDAS EN EL PESCUEZO EN GANSOS DEL CANADA Rcsumcn.--Gansos dcl Canada (Branta canadensis) marcados cn cl Rio McConncll (Canada), con bandas cn cl pcscuczo, fucron rccapturados con mcnor frccucncia quc gansos anillados cn sus patas. La difcrcncia pucdc scr atribuida a mayor mortalidad dc los gansos quc fucron anillados cn cl pcscuczo, o a la migraci6n dc cstos (particularmcntc machos) a otras fircas dc anidajc. La data obtcnida no pucdc difcrcnciar entre posiblcs causas, dado cl hccho dc quc otros factorcs confundcn cl an/tlisis. Los cazadorcs pot cjcmplo, rccobraron la misma proporci6n dc gansos anillados cn cl pcscuczo cn las patas, aunquc csto podrla scr cl resultado dc informar con prcfcrcncia a aves con marcas cn cl pcscuczo, o a cl prcfcrir cazar aves con una marca bicn visible. No sc cncontraron cfcctos dctrimcntalcs cn la rcproducci6n dc aves quc fucron anilladas cn cl pcscuczo. E1 posiblc cfccto dc anillas cn cl pcscuczo dcbc scr considcrada cn cl discrio dc cualquicr cstudio quc incluya cl uso dc las mismas. Neck bands can provide special insight into the long-term reproductive performance and survival of geese, provided that the bands themselves do not affect the parameters under study. Neck bands may increase mortality (Ankney 1975, 1976; Zicus et al. 1983), reduce frequency of nesting (Lensink 1968, although based on very small samples), or influence aggressivencounters (Hawkins and Simpson 1985). However, those papers describe specific instances, and there is uncertainty about whether all goose species are affected in all studies. Reproduction may not be affected at all (Chabreck and Shroer 1975). Macinnes and Lieff (1968) reported that neck-banded Canada Geese (Branta canadensis, of a small race in the hutchinsii-parvipes complex, Macinnes 1966) were recaptured at lower rates that leg-banded geese. Here we re-examine the problem in greater detail, including data from later years. We investigated mortality, based on hunter recoveries, recapture rate on the breeding grounds and effect of neck bands on pairing and reproduction. 239

240] c. D. Macinnes and E. H. Dunn J. Field Ornithol. Summer 1988 METHODS Canada Geese were caught during their primary molt at the McConnell River, Northwest Territories (60ø50'N, 94ø25'W) from 1964-1971 (see Macinnes et al. 1974). All unbanded birds were given U.S. Fish and Wildlife Service aluminum leg bands. In addition, neck bands were put on some adults in 1964, and in later years, on all birds large enough to retain them. We kept goslings in a separate holding pen so that all adults and young could be released together; goslings too small to retain neck bands shed them there. Neck bands applied in 1964-1965 were plastic, whereas later bands were aluminum (Macinnes et al. 1969). Any bird captured after 1965 was given a new metal neck band if the old one was plastic, defaced, or lost, or if the bird had not previously had a neck band. Recapture of a bird was tallied only on the first instance of capture in a year subsequento the year of banding. If a leg-banded goose was later recaptured and given a neck band, it was recorded as a leg-band recapture, but was then added to the pool of newly neck-banded birds so that it might later be encountered as a recaptured neck band. Neither recapture nor recovery rate differed between the plastic and metal neck bands, so results are combined in this paper. However, we arbitrarily chose to tally as neck-banded all birds that had lost neck bands before recapture or recovery. Although aluminum neck bands were almost never lost ((0.1% annually), about 2 $ % of plastic neck bands fell off each year. Our arbitrary correction may therefore have masked an additional effect of plastic neck bands. We observed geese from elevated towers, and throughout the day we counted broods in families with one or both adults neck-banded. Brood counts of pairs without neck bands were derived from surveys made during early morning and late evening, when visibility was best (Macinnes et al. 1974). In this paper, comparisons of brood counts between unbanded and neck-banded pairs were made for the one day each season on which the largest number of broods was seen (always within the week just before banding began). Because pairs without neck bands that had lost whole broods could not be identified as such, comparison of brood size was made only for pairs with at least one gosling. RESULTS Recovery rate of geese neck-banded as adults was similar to that for adults leg-banded alone (Table 1; P y 0.05; X2 corrected for continuity, Snedecor and Cochrane ]967). Neither recovery rate differed between the sexes. Annual recovery rates of neck-banded adults ranged from 20-33%, but did not vary significantly among years (? y 0.05). Similarly, leg-banded goslings from 1964 (when all sizes of gosling were leg-banded only) were not recovered at different rates than neck-banded goslings, and the sexes did not differ. Recovery rates of gosling females leg-banded in 1965-1971, when only small individuals were given leg bands alone, were lower than those of

Vol. 9, No. 3 Effects of Neck Bands on Canada Geese [241 Tt BL. 1. Percent of Canada Geese banded at the McConnell River that were recovered dead elsewhere. Band type b Gosling Adult (both sexes) Male Female No. Percent No. Percent No. Percent banded recovered banded recovered banded recovered Neck band (1964-1971) 1102 26 611 29 540 33 Leg band (1964) 39 33 87 21 88 23 Leg band (1965-1971) -- -- 350 23 557 17 Recoveries reported to the Bird Banding Laboratory (U.S. Fish & Wildlife Service) through 1983. Numbers of leg-banded birds include only those birds never given a neck band (i.e., never recaptured). b All goslings banded in 1964 received leg bands alone, whereas in 1965-1971 only those too small to retain a neck band were given a leg band alone. leg-banded males from the same years and lower than those of neckbanded goslings of both sexes (? < 0.05). Recapture rates on the nesting ground were compared only for 1965-1969, as geese banded in the last 2 yr of study had little chance of being recaptured. Adults leg-banded in 1964 were recaptured twice as frequently on the breeding grounds as neck-banded adults (P < 0.005, Table 2), and there were no differences in rates between the sexes. Similarly, gosling females leg-banded in 1964 were recaptured at a much higher rate than gosling females neck-banded in later years. Gosling females legbanded in other years, however, when only small individuals were legbanded, had similar recapture rates to neck-banded gosling females. Recapture rates of gosling males did not differ among band types. In all cases, differences in recapture rates showed in the first summer following the year of banding. Once leg-banded adults had been recaptured once and given a neck band, they did not differ in subsequent recapture rates from originally neck-banded birds that had also been recaptured once. If both members of a breeding pair were neck-banded, the pair initiated egg-laying one day later than unmarked pairs (P = 0.02, Table 3). Pairs with only the male neck-banded also tended to nest a day later (P = 0.08), whereas pairs with only the female neck-bande did not, suggesting that the delay of egg-laying was affected by the males. There were no significant differences in clutch size, despite different initiation dates (Table 3). Brood size at about three weeks of age was compared for neck-banded and unmarked pairs. In three of the four years with data there was no difference in brood size, but in the fourth, neck-banded pairs averaged one less gosling than unmarked pairs (P = 0.04, Table 4). DISCUSSION The combination of low recovery (Table 1) and recapture rates (Table 2) of female goslings leg-banded after 1964 (when only small birds received leg bands alone) suggested that those birds were subjecto high

242] C. D. Madnnes and E. H. Dunn j. Field Ornithol. Summer 1988 T^BLE 2. Recapture and recovery rates of Canada Geese banded at the McConnell River, by band type, age, and sex. a Percent of total Recap- Not tured recaptured at the Recovered or Age and sex Total McCon- without recovered at banding Band type b banded nell recapture (% seen c) Adult Neck band (1964-1969) 1043 20 21 58 (20) Gosling male Gosling female Leg band (1964) 66 42 20 38 Neck band (1965-1969) 399 5 26 66 (13) Leg band (1964) 95 4 21 75 Leg band (1965-1969) 302 4 25 71 Neck band (1965-1969) 407 7 36 57 (11) Leg band (1964) 107 18 19 64 Leg band (1965-1969) 440 6 18 76 a Asterisks between values indicate significant differences (X 2, P < 0.05 = *, P < 0.005 b Leg bands alone were put on all goslings in 1964, but thereafter only on goslings too small to retain a neck band. c Percent of neck-banded birds identified by neck-band code at the McConnell River, but never recaptured or recovered. mortality before the beginning of their first hunting season. Such early mortality may have been natural, related to the birds' smaller size, or could have resulted from the mass-banding process itself. It is not clear why the effect was absent in undersized males, but our recapture samples are small. The particularly low recapture rate of all gosling males supports the hypothesis that young males mate during spring migration and follow their chosen female to her natal area (Macinnes and Lieff 1968). Because of the special nature of goslings receiving leg bands alone in 1965-1971, it is only appropriate to compare recovery and recapture rates of neck-banded goslings with those for leg-banded goslings from 1964 (a fact not appreciated in Macinnes et al. 1974:701). Similarly, adult data can only be compared to leg-band data from 1964, as that was the only year when leg bands alone were applied. The following discussion is based on the assumption that the 1964 leg-band sample was indeed representative, and not influenced by factors peculiar to that year. Neck-banded birds were generally recaptured at half the rate of 1964 leg-banded birds (Table 2). One possible cause is reduced catchability. There were relatively large numbers of neck-banded geese seen at McConnell that were never recaptured or recovered (Table 2). However, we think it very unlikely that neck-banding a bird should have made it markedly less catchable than leg-banding, as trapping and handling pro-

Vol. 59, No. 3 Effects of Neck Bands on Canada Geese [243 TABLE 3. Effect of neck band status on date of clutch initiation and clutch size. a Differ- Date of clutch initiation ence Source of from variation mean b F n P Neck-banded male only 1.49 3.07 14, 69 0.08 Neck-banded female only -0.49 0.73 30, 69 0.40 Neck-banded male x neck-banded female 1.15 5.54 68, 69 0.02 Clutch size Neck-banded male only -0.11 0.10 14, 69 0.75 Neck-banded female only 0.20 0.75 30, 69 0.39 Neck-banded male x neck-banded female -0.16 0.75 115, 69 0.39 a ANOVA of date of clutch initiation and clutch size with year and marking status of pair. All comparisons made with pairs in which neither bird was neck-banded. Year had a significant effect in each ANOVA (not shown in table). Column headings starting with F are: F-ratio, sample size, probability. b Difference from mean value for pairs without either adult neck-banded (n = 69), after correction for independent effects of year. A negative date of first egg indicates earlier nest initiation. cedures were otherwise the same. Moreover, there was no increase in the numbers of birds seen but not recaptured over the course of the study, as would be expected if catchability of neck-banded birds was reduced. We assume for the remainder of this discussion that neck bands had some other effect. Low recapture of neck-banded geese could indicate either higher mortality or lowered likelihood of returning to nest in the McConnell area. If reproductive behavior was disrupted, then birds might have left the McConnell area prior to banding drives. Alternatively, neck-banded birds TABLE 4. Effect of neck band status on brood size. a 1967 Mean brood Year size b F n P Neck-banded pairs 2.76 4.86 17 0.04 Non-neck-banded pairs 3.87 16 1968-1970 Neck-banded pairs 3.18 1.59 56 0.21 Non-neck-banded pairs 3.50 34 a ANOVA of pairs with either or both birds neck-banded compared to pairs with no neck bands. Only pairs with at least one gosling were included in the analysis. Column headings as in Table 3. Corrected for year, which had a highly significant effect in the multi-year analysis.

244] C. D. Macinnes and E. H. Dunn J. Field Ornithol. Summer 1988 might have emigrated and bred elsewhere. Other analyses of the effects of markers have sometimes ignored this range of possibilities (e.g., Howe 1980). Increased non-hunting mortality or reduced chance of recapture at the McConnell area should be distinguishable by their different effects on recovery and recapture rates, as shown in Table 5. Unfortunately, there are two important biases that could alter recovery rates, making it difficult to interpret our results. Hunters may be more likely to report neck-banded than leg-banded birds to the Bird Banding Laboratory, and hunters may selectively shoot visibly marked geese (Craven 1979). Either bias would increase the recovery rate of neck-banded geese, but only hunter selectivity would decrease the recapture rate of these birds. Raveling (1978) estimated a reporting rate of neck-banded Canada Goose recoveries similar to that for leg-banded birds, but Craven (1979) found nearly twice the recovery rate of neck-banded over leg-banded Canada Geese in two of four years. Craven found no difference in recapture rates in a single sample of 51 recaptured birds, suggesting that reporting bias was important. As 20-25% of hunters in Craven's study reported being conscious of seeing neckbands before they shot, hunter selection may also have been important. We conclude that there is no clear evidence from other studies to help us estimate the importance of potential biases in our own data. Predicted effects of these biases in combination with possible effects of neck bands are shown in Table 5. The tabulated predictions are mutually exclusive for each set of conditions described, but in reality several of these effects may be confounded. Our data for geese neck-banded as adults are consistent with the predictions for neck bands causing mortality, combined with reporting bias. Data for neck-banded female goslings better fit the predictions for reduced chance of nesting at the McConnell River, combined with reporting or selection bias in the data. Male goslings were apparently unaffected by neck bands, but their low rate of return to the McConnell area gave us very small samples. It would be surprising if neck bands had very different effects on adults than on goslings, and neck bands seem more likely to cause some combination of mortality and/or disruption of breeding in both groups. Although about half the neck-banded birds were affected, it is important to keep in mind that at least some of these may have nested normally away from the McConnell River study area. We have assumed thus far that our sample of leg-banded geese is adequate, despite its short (1 yr) sample period. This problem, combined with possible biases in recovery rates, makes it impossible to determine conclusively whether neck bands had negative effects on Canada Geese. Our data are suggestive but should not be taken as certain evidence that neck-banding causes mortality and/or disruption of breeding. Our support is good, however, for the conclusion that neck bands did not negatively affect performance of those neck-banded birds that did return to nest at the McConnell River study area. New mates with and without neck bands were chosen in proportion to their numbers in the study area,

Vol. 59, o. 5 Effects of Neck Bands on Canada Geese [245 TABLE 5. Predictions for signs of ratios of recapture and recovery rates of neck-banded geese to those of leg-banded geese; with and without assumption of positive reporting bias or hunter selectivity of neck-banded birds (see text). Zero indicates prediction of the same rates for both groups, - - indicates particularly severe effect of neck bands. Parentheses mean that predictions would depend on degree of difference in other rates. Table 2 data Effect of neck bands Recap- Neither Recovery tured Recovered recovered rate at mc- without nor (Table 1) Connell recapture recaptured None 0 0 0 0 With report bias q- 0 q- - With selection bias + - + (0) Mortality - - - + With report bias (0) - (0) (+) With selection bias (0) (0) - Reduced chance of breeding at McConnell 0 - + (0) With report bias + - + (0) With selection bias + + (0) indicating that pair formation was not affected by neck bands. The proportion of neck-banded non-breeders remaining on the nesting area was also similar to that in leg-banded populations (Macinnes and Dunn 1988). We have suggested that neck bands may cause important non-hunting mortality in Canada Geese, result in birds moving away from the breeding area (where they may or may not breed), or perhaps reduce catchability of neck-banded geese that have returned to nest. Such effects should be considere during analysis and interpretation of studies in which geese are neck-banded. Reporting bias and hunter selection of marked birds will unfortunately confound such analyses. It is therefore important to test the effects of neck bands as an integral part of each study of neckbanded geese, rather than post-facto, as in this paper. Investigators must plan carefully, so that adequate samples of marked and unmarked birds are encountered in the years following banding. Although we were unable to provide conclusive evidence of negative effects of neck-banding, we hope our discussion of the difficulties in assessing such effects will stim- ulate others to undertake more extensive studies. ACKNOWLEDGMENTS We are grateful (in retrospect) to the anonymous reviewer of another of our manuscripts, who prompted us to undertake this detailed analysis. This is Ontario Ministry of Natural Resources, Wildlife Research Contribution No. 86-08. LITERATURE CITED ANKNEY, C. D. 1975. Neck bands contribute to starvation in female Lesser Snow Geese. J. Wildl. Manage. 39:825-826. 1976. Response by C. D. Ankney. J. Wildl. Manage. 40:572.

246] C. D. Macinnes and E. H. Dunn J. Field Ornithol. Summer 1988 CtqABRECK, R. H., AND J. D. SHROER. 1975. Effects of neck collars on the reproduction of Snow Geese. Bird-Banding 46:346-347. CRAVEN, S. R. 1979. Some problems with Canada Goose neckbands. Wildl. Soc. Bull. 7: 268-273. HAWKINS, L. g., AND S. G. SIMPSON. 1985. Neckband a handicap in an aggressivencounter between Tundra Swans. J. Field Ornithol. 56:182-184. HOWE, M. A. 1980. Problems with wing tags: evidence of harm to Willets. J. Field Ornithol. 51:72-73. LENSINK, C.J. 1968. Neck bands as an inhibitor of reproduction in Black Brant. J. Wildl. Manage. 32:418-420. MACINNES, C. D. 1966. Population behavior of eastern Arctic Canada Geese. J. Wildl. Manage. 30:536-553., R. A. DAVIS, R. N. JONES, B.C. LIEFF, AND A. J. PAKULAK. 1974. Reproductive efficiency of McConnell River small Canada Geese. J. Wildl. Manage. 38:686-707., AND E. H. DUNN. 1988. Estimating proportion of an age class nesting in Canada Geese. J. Wildl. Manage. 52:421-423., AND B.C. LIEFF. 1968. Individual behavior and composition of a local population of Canada Geese. Pp. 93-101, in R. L. Hine and C. Schoenfeld, eds. Canada Goose management. Dembar Educational Research Services, Madison, Wisconsin., J.P. PREVETT, AND H. A. EDNEY. 1969. A versatile collar for individual identification of geese. J. Wildl. Manage. 33:330-335. RAVELING, D.G. 1978. Dynamics of distribution of Canada Geese in winter. Trans. N. Am. Wildl. Nat. Resour. Conf. 43:206-225. SNEDECOR, G. W., AND W. G. COCHRAN. 1967. Statistical methods, sixth edition. Iowa State University Press, Ames, Iowa. ZICUS, M. C., D. F. SCHULTZ, AND J. A. COOPER. 1983. Canada Goose mortality from neckband icing. Wildl. Soc. Bull. 11:286-290. Received 11 May 1987; accepted 21 Nov. 1987.