Thomas Fondell - Academia.edu (original) (raw)

Papers by Thomas Fondell

Canadian Journal of Zoology, May 26, 2014

ABSTRACT A total of 842 blood samples collected from five species of tundra-nesting geese in Alas... more ABSTRACT A total of 842 blood samples collected from five species of tundra-nesting geese in Alaska was screened for haemosporidian parasites using molecular techniques. Parasites of the genera Leucocytozoon Danilewsky, 1890, Haemoproteus Kruse, 1890, and Plasmodium Marchiafava and Celli, 1885 were detected in 169 (20%), 3 (<1%), and 0 (0%) samples, respectively. Occupancy modeling was used to estimate prevalence of Leucocytozoon parasites and assess variation relative to species, age, sex, geographic area, year, and decade. Species, age, and decade were identified as important in explaining differences in prevalence of Leucocytozoon parasites. Leucocytozoon parasites were detected in goslings sampled along the Arctic Coastal Plain using both historic and contemporary samples, which provided support for transmission in the North American Arctic. In contrast, lack of detection of Haemoproteus and Plasmodium parasites in goslings (n = 238) provided evidence to suggest that the transmission of parasites of these genera may not occur among waterfowl using tundra habitats in Alaska, or alternatively, may only occur at low levels. Five haemosporidian genetic lineages shared among different species of geese sampled from two geographic areas were indicative of interspecies parasite transmission and supported broad parasite or vector distributions. However, identical Leucocytozoon and Haemoproteus lineages on public databases were limited to waterfowl hosts suggesting constraints in the range of parasite hosts.

Journal of Field Ornithology, 2004

... THOMAS F. FONDELL , 1 , JAMES B. GRAND , , DAVID A. MILLER , , and R. MICHAEL ANTHONY. (2006)... more ... THOMAS F. FONDELL , 1 , JAMES B. GRAND , , DAVID A. MILLER , , and R. MICHAEL ANTHONY. (2006) Renesting by Dusky Canada Geese on the Copper River Delta, Alaska. Journal of Wildlife Management 70:4, 955-964 Online publication date: 1-Oct-2006. ...

Wildlife Monographs, 2006

Wildlife Biology, 2006

2006: Techniques for identifying predators of goose nests. -Wildl. Biol. 12: 249-256.

Virology Journal, 2008

The global spread of the highly pathogenic avian influenza H5N1 virus has stimulated interest in ... more The global spread of the highly pathogenic avian influenza H5N1 virus has stimulated interest in a better understanding of the mechanisms of H5N1 dispersal, including the potential role of migratory birds as carriers. Although wild birds have been found dead during H5N1 outbreaks, evidence suggests that others have survived natural infections, and recent studies have shown several species of ducks capable of surviving experimental inoculations of H5N1 and shedding virus. To investigate the possibility of migratory birds as a means of H5N1 dispersal into North America, we monitored for the virus in a surveillance program based on the risk that wild birds may carry the virus from Asia.

The Wilson Bulletin, 2002

ABSTRACT We studied orientation of nest sites relative to nearby vegetation for dabbling ducks (C... more ABSTRACT We studied orientation of nest sites relative to nearby vegetation for dabbling ducks (Cinnamon Teal, Anas cyanoptera; Blue-winged Teal, A. discors; Gadwall, A. strepera; Mallard, A. platyrhynchos; and Northern Shoveler, A. clypeata) and Short-eared Owls (Asio flammeus) in ungrazed grassland habitat during 1995–1997 in westcentral Montana. We estimated an index of vegetation height and density in intercardinal directions (NE, SE, SW, NW) immediately around nests. All species oriented nests with the least vegetation to the southeast and the most vegetation to either the southwest or northwest. Furthermore, maximum vegetation around nests shifted from the southwest to the northwest with increasing nest initiation date, apparently as a response of individuals tracking seasonal change in the afternoon solar path. Thus, nests were relatively exposed to solar insolation during cool morning hours but were shaded from intense insolation in the afternoon throughout the breeding season. We suggest that nest microhabitat was selected in part to moderate the thermal environment.

Journal of Wildlife Management, 2006

The population of dusky Canada geese (Branta canadensis occidentalis; hereafter duskies) breeding... more The population of dusky Canada geese (Branta canadensis occidentalis; hereafter duskies) breeding on the Copper River Delta (CRD), Alaska, USA, has been in long-term decline, largely as a result of reduced productivity. Estimates of renesting rates by duskies may be useful for adjusting estimates of the size of the breeding population derived from aerial surveys and for understanding population dynamics. We used a marked population of dusky females to obtain estimates of renesting propensity and renesting interval on the CRD, 1999CRD, -2000. Continuation nests, replacement nests initiated without a break in the laying sequence, resulted only after first nests were destroyed in the laying stage with 4 eggs laid. Renesting propensity declined with nest age from 72% in mid-laying to 30% in early incubation. Between first nests and renests, mean interval was 11.9 6 0.6 days, mean distance was 74.5 m (range 0-214 m), and clutch size declined 0.9 6 0.4 eggs. We incorporated our renesting estimates and available estimates of other nesting parameters into an individual-based model to predict the proportion of first nests, continuation nests, and renests, and to examine female success on the CRD, 1997CRD, -2000. Our model predicted that 19-36% of nests each year were continuation nests and renests. Also, through 15 May (the approx. date of breeding ground surveys), 1.1-1.3 nests were initiated per female. Thus, the number of nests per female would have a significant, though relatively consistent, effect on adjusting the relation between numbers of nests found on ground surveys versus numbers of birds seen during aerial surveys. We also suggest a method that managers could use to predict nests per female using nest success of early nests. Our model predicted that relative to observed estimates of nest success, female success was 32-100% greater, due to replacement nests. Thus, although nest success remains low, production for duskies was higher than previously thought. For dusky Canada geese, managers need to consider both continuation nests and renests in designing surveys and in calculating adjustment factors for the expansion of aerial survey data using nest densities. (JOURNAL OF WILDLIFE MANAGEMENT 70(4):955-964; 2006)

The Journal of Wildlife Management, 2011

Recent declines in black brant (Branta bernicla nigricans) are likely the result of low recruitme... more Recent declines in black brant (Branta bernicla nigricans) are likely the result of low recruitment. In geese, recruitment is strongly affected by habitat conditions experienced by broods because gosling growth rates are indicative of forage conditions during brood rearing and strongly influence future survival and productivity. In 2006-2008, we studied gosling growth at 3 of the 4 major colonies on the Yukon-Kuskokwim Delta, Alaska. Estimates of age-adjusted gosling mass at the 2 southern colonies (approx. 30% of the world population of breeding black brant) was low (gosling mass at 30.5 days ranged 346.7 AE 42.5 g to 627.1 AE 15.9 g) in comparison to a third colony (gosling mass at 30.5 days ranged 640.0 AE 8.3 g to 821.6 AE 13.6 g) and to most previous estimates of age-adjusted mass of brant goslings. Thus, our results are consistent with the hypothesis that poor gosling growth is negatively influencing the brant population. There are 2 non-mutually exclusive explanations for the apparent growth rates we observed. First, the population decline may have been caused by density-independent factors and habitat capacity has declined along with the population as a consequence of the unique foraging feedback between brant and their grazing habitats. Alternatively, a reduction in habitat capacity, as a result of changes to the grazing system, may have negatively influenced gosling growth, which is contributing to the overall long-term population decline. We found support for both explanations. For colonies over habitat capacity we recommend management to enhance foraging habitat, whereas for colonies below habitat capacity we recommend management to increase nesting productivity. ß 2011 The Wildlife Society.

Journal of Field Ornithology, 2008

The population of Dusky Canada Geese (Branta canadensis occidentalis) has been in long-term decli... more The population of Dusky Canada Geese (Branta canadensis occidentalis) has been in long-term decline, likely due to reduced breeding productivity. To identify causes of mortality, we monitored goslings marked with radio transmitters on the western Copper River Delta, Alaska, from 1997 to 1999. Almost all gosling mortality (96%; 81 of 84) was due to predation, with mink (Mustela vison) and Bald Eagles (Haliaeetus leucocephalus) the most important predators. Bald Eagles are also major nest predators and, thus, appear to play a key role in limiting the breeding productivity of Dusky Canada Geese. Daily survival rate for goslings to 28 d of age was lower (0.011; 95% CI 0.002−0.024) for those with transmitters than for those without, but did not differ for older goslings (29−45 d).

Journal of Animal Ecology, 2006

Predation plays an integral role in many community interactions, with the number of predators and... more Predation plays an integral role in many community interactions, with the number of predators and the rate at which they consume prey (i.e. their functional response) determining interaction strengths. Owing to the difficulty of directly observing predation events, attempts to determine the functional response of predators in natural systems are limited. Determining the forms that predator functional responses take in complex systems is important in advancing understanding of community interactions. 2. Prey survival has a direct relationship to the functional response of their predators. We employed this relationship to estimate the functional response for bald eagle Haliaeetus leucocepalus predation of Canada goose Branta canadensis nests. We compared models that incorporated eagle abundance, nest abundance and alternative prey presence to determine the form of the functional response that best predicted intra-annual variation in survival of goose nests. 3. Eagle abundance, nest abundance and the availability of alternative prey were all related to predation rates of goose nests by eagles. There was a sigmoidal relationship between predation rate and prey abundance and prey switching occurred when alternative prey was present. In addition, predation by individual eagles increased as eagle abundance increased. 4. A complex set of interactions among the three species examined in this study determined survival rates of goose nests. Results show that eagle predation had both prey-and predator-dependent components with no support for ratio dependence. In addition, indirect interactions resulting from the availability of alternative prey had an important role in mediating the rate at which eagles depredated nests. As a result, much of the within-season variation in nest survival was due to changing availability of alternative prey consumed by eagles. 5. Empirical relationships drawn from ecological theory can be directly integrated into the estimation process to determine the mechanisms responsible for variation in observed survival rates. The relationship between predator functional response and prey survival offers a flexible and robust method to advance our understanding of predatorprey interactions in many complex natural systems where prey populations are marked and regularly visited.

The Condor, 2007

We examined the relationship between attributes of nest sites used by Canada Geese (Branta canade... more We examined the relationship between attributes of nest sites used by Canada Geese (Branta canadensis) in the Copper River Delta, Alaska, and patterns in nest and female survival. We aimed to determine whether nest site attributes related to nest and female survival differed and whether nest site attributes related to nest survival changed within and among years. Nest site attributes that we examined included vegetation at and surrounding the nest, as well as associations with other nesting birds. Optimal nest site characteristics were different depending on whether nest survival or female survival was examined. Prior to 25 May, the odds of daily survival for nests in tall shrubs and on islands were 2.92 and 2.26 times greater, respectively, than for nests in short shrub sites. Bald Eagles (Halieaeetus leucocephalus) are the major predator during the early breeding season and their behavior was likely important in determining this pattern. After 25 May, when eagle predation is limited due to the availability of alternative prey, no differences in nest survival among the nest site types were found. In addition, nest survival was positively related to the density of other Canada Goose nests near the nest site. Although the number of detected mortalities for females was relatively low, a clear pattern was found, with mortality three times more likely at nest sites dominated by high shrub density within 50 m than at open sites dominated by low shrub density. The negative relationship of nest concealment and adult survival is consistent with that found in other studies of groundnesting birds. Physical barriers that limited access to nest sites by predators and sites that allowed for early detection of predators were important characteristics of nest site quality for Canada Geese and nest site quality shifted within seasons, likely as a result of shifting predator-prey interactions.

The Auk, 2006

AяѠѡџюѐѡ.-The Dusky Canada Goose (Branta canadensis occidentalis) population that breeds in the C... more AяѠѡџюѐѡ.-The Dusky Canada Goose (Branta canadensis occidentalis) population that breeds in the Copper River Delta, Alaska, has declined substantially since the late 1970s. Persistent low numbers have been aĴ ributed to low productivity in recent years. We examined paĴ erns in survival rates of 1,852 nests to beĴ er understand ecological processes that infl uenced productivity during 1997-2000. We compared 10 nonparametric models of daily survival rate of nests (DSR) that included variation among years, calendar dates, nest initiation dates, and nest ages with equivalent models based on parametric functions. The unequivocal best model included paĴ erns of DSR that varied among discrete periods of years, calendar dates, and nest ages. Generally, DSR was low early in the nesting season and higher midseason. Across years, paĴ erns in DSR were most variable early and late in the nesting season. Daily survival rates of nests declined between the fi rst and second week aĞ er initiation, increased until the fourth week, and then declined during the last week before hatch. Nest survival probability estimates ranged from 0.07 to 0.71 across years and nest initiation dates. Mean rates of nest survival ranged between 0.21 and 0.31 each year. We suggest (1) considering models that do not limit estimates of daily nest survival to parametric forms; (2) placing greater emphasis on sample size when nests are rare, to obtain accurate estimates of nest survival; and (3) developing new techniques to estimate the number of nests initiated.

The dusky Canada goose (Branta canadensis occidentalis) population has been in long-term decline,... more The dusky Canada goose (Branta canadensis occidentalis) population has been in long-term decline, likely due to reduced breeding productivity, but gosling survival of this population had not been examined. We studied gosling survival in broods of radiomarked adult females on the western Copper River Delta, Alaska, USA, during 1997USA, during -1999USA, during and 2001USA, during -2003. Survival estimates for dusky Canada goose goslings to 45 days (x ¼ 0.32) were below estimates from most previous studies of geese. Daily survival of goslings increased with age and decreased with date of hatch. Precipitation during the first 3 days post-hatch was negatively related to gosling survival and this effect increased with date. Annual estimates of gosling survival were positively correlated with annual estimates of nest success, suggesting overlap in factors affecting nest and gosling survival. Nest success probably also directly affected gosling survival, because survival decreased with hatch date and more broods hatched from renests during years with low nest success. Gosling survival appears to play an important role in limiting current productivity of this population. Management directed at increasing nest success would likely also improve gosling survival. We recommend additional research directed at examining sources of gosling mortality and the link between nest success and gosling survival.

ABSTRACT Birds employ varying strategies to accommodate the energetic demands of moult, one impor... more ABSTRACT Birds employ varying strategies to accommodate the energetic demands of moult, one important example being changes in body mass. To understand better their physiological and ecological significance, we tested three hypotheses concerning body mass dynamics during moult. We studied Black Brant in 2006 and 2007 moulting at three sites in Alaska which varied in food availability, breeding status and whether geese undertook a moult migration. First we predicted that if mass loss during moult were simply the result of inadequate food resources then mass loss would be highest where food was least available. Secondly, we predicted that if mass loss during moult were adaptive, allowing birds to reduce activity during moult, then birds would gain mass prior to moult where feeding conditions allowed and mass loss would be positively related to mass at moult initiation. Thirdly, we predicted that if mass loss during moult were adaptive, allowing birds to regain flight sooner, then across sites and groups, mass at the end of the flightless period would converge on a theoretical optimum, i.e. the mass that permits the earliest possible return to flight. Mass loss was greatest where food was most available and thus our results did not support the prediction that mass loss resulted from inadequate food availability. Mass at moult initiation was positively related to both food availability and mass loss. In addition, among sites and years, variation in mass was high at moult initiation but greatly reduced at the end of the flightless period, appearing to converge. Thus, our results supported multiple predictions that mass loss during moult was adaptive and that the optimal moulting strategy was to gain mass prior to the flightless period, then through behavioural modifications use these body reserves to reduce activity and in so doing also reduce wing loading. Geese that undertook a moult migration initiated moult at the highest mass, indicating that they were more than able to compensate for the energetic cost of the migration. Because Brant frequently change moult sites between years in relation to breeding success, the site‐specific variation in body mass dynamics we observed suggests individual plasticity in moult body mass dynamics.