USGS ScienceSearch

Geology topics

William J.L. Sladen

Publications and source records attributed to William J.L. Sladen.

8 recordsLinked to original sources

Delineation of Tundra Swan Cygnus c. columbianus populations in North America: geographic boundaries and interchange

North American Tundra Swans Cygnus c. columbianus are composed of two wellrecognised populations: an Eastern Population (EP) that breeds across northern Canada and north of the Brooks Range in Alaska, which migrates to the eastern seaboard of the United States, and a Western Population (WP) that breeds in coastal regions of Alaska south of the Brooks Range and migrates to western North America. We present results of a recent major ringing effort from across the breeding range in Alaska to provide a better definition of the geographic extent of the migratory divide in Alaska. We also reassess the staging and winter distributions of these populations based on locations of birds tracked using satellite transmitters, and recent recoveries and sightings of neck-collared birds. Summer sympatry of EP and WP Tundra Swans is very limited, and largely confined to a small area in northwest Alaska. Autumn migration pathways of EP and WP Tundra swans abut in southwest Saskatchewan, a region where migrating WP birds turn west, and EP birds deviate abruptly eastward. Overall, from 1989 to 2013 inclusive, 2.6% of recoveries or resightings reported to the USGS Bird Banding Laboratory were of birds that moved from the domain of the population in which they were initially captured to within the range of the other population; a proportion roughly comparable to the results of Limpert et al . (1991) for years before 1990. Of the 70 cross-boundary movements reported since 1989, 39% were of birds marked on breeding areas and 61% were of birds marked on wintering areas. Dispersing swans (i.e. those that made crossboundary movements) did not differ with respect to age or sex from those that did not move between populations. The Brooks Range in northern Alaska effectively separates the two populations within Alaska, but climate-induced changes in tundra breeding habitats and losses of wetlands on staging areas may alter the distribution for both of these populations.

Wildfowl

Motorized migrations: The future or mere fantasy?

In 15 experiments from 1993-2002, we led cranes, geese, or swans on their first southward migration with either ultralight aircraft or vehicles on the ground. These experiments reveal that large birds can be readily trained to follow and most will return north (and south) in subsequent migrations unassisted. These techniques can now be used to teach birds new (or forgotten) migration paths. Although we are constantly improving our training techniques, we now have an operational program that can be broadly applied to those species where juveniles learn migration routes from their parents.

Arizona, Florida, Idaho, Indiana, Maryland, New Me

Teaching migration routes to canada geese and trumpeter swans using ultralight aircraft, 1990-2001

This paper summarizes eleven years (1990-2001) of experiments to teach Canada Geese (Branta canadensis) and Trumpeter Swans (Cygnus buccinator) pre-selected migration routes using ultralight aircraft. When Canada Geese were trained to follow an ultralight aircraft for southward autumn migrations of 680 or 1,320 km, 81% (83/103) returned on their own in the next spring to near their place of training. In contrast, none returned of 21 similarly raised geese that were transported south in a closed truck over a route of 680 km. Trumpeter Swans have proven more difficult to train. However, in two experiments in which Trumpeter Swans followed an ultralight for the entire pre-selected route, one of three and two of four returned close to their training area. A stage-by-stage method, in which swans were transported in trucks between stops, flown in the vicinity and penned with a view of the night sky, has shown some promise. So far an established migration route (north and south twice) has been confirmed in only two geese

Book chapter

Baseline hematology and clinical chemistry results from captive-raised trumpeter swans

Results from hematology and clinical chemistry tests are presented for healthy captive-raised Trumpeter Swans (Cygnus buccinator) to help establish baseline data. Blood samples were obtained from 14 cygnets between the ages of three to four and seven to eight months that were the subjects of a study to teach migration routes to swans. Males and females differed significantly in asparatate aminotransferase, alanine aminotransferase and total protein. Age categories differed significantly in hematocrit, white blood cell counts, alkaline phosphatase, aspar-rate aminotransferase, glucose, cholesterol and uric acid. There were no significant differences among age categories in values of alanine aminotransferase, calcium, triglycerides and total protein.

Book chapter

Lessons from the motorized migrations

Ten experiments have been conducted to determine if cranes can be led on migration and if those so trained will repeat migrations on their own. Results have been mixed as we have experienced the mishaps common to pilot studies. Nevertheless, we have learned many valuable lessons. Chief among these are that cranes can be led long distances behind motorized craft (air and ground), and those led over most or the entire route will return north come spring and south in fall to and from the general area of training. However, they will follow their own route. Groups transported south and flown at intervals along the route will migrate but often miss target termini. If certain protocol restrictions are followed, it is possible to make the trained cranes wild, however, the most practical way of so doing is to introduce them into a flock of wild cranes. We project that it is possible to create or restore wild migratory flocks of cranes by first leading small groups from chosen northern to southern termini.

Book chapter

Annual survival rates of adult and immature eastern population tundra swans

Tundra swans ( Cygnus columbianus) of the eastern population were neckbanded in Maryland, North Carolina, and Alaska from 1966 through 1990. These swans were resighted and recaptured during autumn, winter, and spring, 1966-1990. Although the original motivation for this study involved swan movements, we wanted to use the resulting data to test hypotheses about sources of variation in swan survival rates. Recaptures of legbanded and neckbanded swans permitted us to estimate neckband loss rates, which were found to vary with age and sex of swans, and number of years since initial application. Estimates of annual neckband retention rate ranged from about 0.50 for adult male swans ≥ 2 years after initial neckbanding to > 0.96 for immature swans and adult females the first year following neckbanding. This variation in neckband loss rates prevented the simple correction of survival estimates to account for such loss. Consequently, we developed a series of multinomial models parameterized with survival, sighting, and neckband retention probabilities for use with the recapture and resighting data.

Alaska, Maryland, North Carolina