We investigated fat deposition in transient, nocturnal, long-distance migrants at a wooded stopover site that is not near an ecological barrier (e.g. desert, large water body). The changes in body mass of recaptured birds have traditionally been used as a measure of mass gains at stopover sites. This technique ignores the majority of transients, however, possibly hindering the ability to answer species-level questions regarding stopover mass gain. We compare an analysis of recaptures with a technique that considers all captures and their condition by time of day. Eleven woodland-associated migrant species were analyzed, as well as a resident species (Black-capped Chickadee, Parus atricapillus) for comparison. Based on recapture data alone, our study site appears to be primarily a location of mass loss, rather than one of fat deposition. Conversely, the examination of condition by time of day suggests that individuals of several species have net daily gains greatly exceeding those of recaptured individuals. During autumn, however, several species exhibited net daily losses. Although some of these losses may be related to molt, it seems unlikely that molt is the only contributing factor. Differences among species in mass gains at our site suggest that various fat-deposition patterns (and, thus, migration strategies) may occur among migrants that are not approaching ecological barriers.

During a study of migrating land birds in 1987, we examined over 9,200 individual birds representing 99 species from the Saint Croix River Valley, a Lyme disease-endemic area of east central Minnesota and northwestern Wisconsin. We found that 250 deer tick (Ixodes dammini) larvae and nymphs infested 58 birds from 15 migrant species; 56 ticks (22.4%) were positive for the Lyme disease spirochete Borrelia burgdorferi. Five ground-foraging migrant bird species favoring mesic habitats, veery (Catharus fuscescens), ovenbird (Seiurus aurocapillus), northern waterthrush (S. novaboracensis), common yellowthroat (Geothlypis trichas), and swamp sparrow (Melospiza georgiana), accounted for nearly three-quarters of parasitized individuals. Nearly half of the spirochete-positive ticks were removed from migrating birds taken in a riparian floodplain forest. Recaptured migrants with infected ticks indicate that they transmit B. burgdorferi to hexapod larvae. We suggest that birds may be both an important local reservoir in the upper Mississippi Valley and long-distance dispersal agents for B. burgdorferi-infected ticks to other regions of the continent.

The anterior and posterior ends of the insect embryo are patterned through the terminal patterning system, which is best known from the fruitfly Drosophila melanogaster. In Drosophila, the RTK receptor Torso and its presumed co-activator Torso-like initiate a signaling cascade, which activates two terminal gap genes, tailless and huckebein. These in turn interact with various patterning genes to define terminal structures. Work on other insect species has shown that this system is poorly conserved, and not all of its components have been found in all cases studied. We place the variability of the system within a broader phylogenetic framework. We describe the expression and knock-down phenotypes of the homologues of terminal patterning genes in the hemimetabolous Oncopeltus fasciatus. We have examined the interactions among these genes and between them and other patterning genes. We demonstrate that all of these genes have different roles in Oncopeltus relative to Drosophila; torso-like is expressed in follicle cells during oogenesis and is involved in the invagination of the blastoderm to form the germ band, and possibly also in defining the growth zone; tailless is regulated by orthodenticle and has a role only in anterior determination; huckebein is expressed only in the middle of the blastoderm; finally, torso was not found in Oncopeltus and its role in terminal patterning seems novel within holometabolous insects. We then use our data, together with published data on other insects, to reconstruct the evolution of the terminal patterning gene network in insects. We suggest that the Drosophila terminal patterning network evolved recently in the lineage leading to the Diptera, and represents an example of evolutionary "tinkering", where pre-existing pathways are co-opted for a new function.

ABSTRACT:During a special two-day