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(e.g..Robinson et al. 1995), but to the best of our knowi- nearest 15 cm for nests 53 m above the ground and-Ao <br /> edge these two processes have never, been causally the nearest 0.5 m for rug-her nests. We pooled data <br /> Linked. If nest predation is higher in exotic species. this across vears but anaivzed DMRs of robins and thrushes <br /> may provide one potential mechanism for the popula- separately with the program CONTRAST(Hines&Sauer <br /> tion declines seen in some songbird species occupying 1989). Nests placed in dead trees or shrubs,Rosa multi <br /> this region. For instance, both Mi11s et al. (1989) and flora. and Celastrus spp.,were excluded from the analy- <br /> Germaine et al. (1998) found that native bird species di- ses due to love sample sizes. <br /> versir- and density were positively correlated with the <br /> volume of native vegetation but were negatively corre- <br /> lated or uncorrelated with the voiuine of exotic vegeta- Results <br /> tion. The link between invasion of exotic shrubs and <br /> population declines, if it exists, will take much research We performed pairwise comparisons of daily nest mortal- <br /> to uncover. We examined the connection between ex- iry rate (DMR)between nests built in Lonicera versus na- <br /> otic species and nest predation rates. uve species (including Crataegus and Viburnum as well ` <br /> We document nest predation on two songbird spe- as native tree species, such as Acer, Ostrya, and Prunus) <br /> ties, American Robins (Turdus migratorius) and Wood and built in Rhamnus versus native species. Nests built <br /> Thrushes (Hylocichla mustelina), over 6 years in an ur in Lonicera had significantly higher DMRs than nests in <br /> ban reserve outside of Chicago. Both Lonicera and natives for both robins ()(2 = 12.31, df = 1,p < 0.001; <br /> Rhamnus (predominantly R. cathartica) are abundant Fig. 1) and thrushes (X2 = 4.0. df = 1,p < 0.05; Fig. 1), # <br /> at the site where they have replaced native species of whereas nests built in Rhamnus did not have higher <br /> Viburnum and Crataegus. Rhamnus lack the sharp DMRs than natives for either species (p > 0.25;Fig. 1). <br /> thorns that characterize Crataegus, whereas Lonicera As a potential explanation for these results, we tested <br /> has sturdy branches and reduced basal cover relative to for an effect of nest height in robins (thrushes showed <br /> Viburnum (K.A.S., personal observations). We hvpothe- too little variability in nest height for an analysis) with <br /> size that these features may increase nest predation di- regression analysis. Daily mortalir- rate, calculated from <br /> recth, through predator facilitation. Furthermore, early a minimum of five nest attempts per height category, <br /> leaf flush and expansion in Lonicera maackii (Trisel & was inversely related to nest height (r2 = 0.496, p = <br /> Gorchov 1994) may make them a focus for nest build- 0.001; Fig. 2). Moreover, the proportion (aresin-square- <br /> ing. Concentrating nest densities by nesting in a re- root-transformed) of depredated nests(minimum of four <br /> stricted subset of plant types available may in turn at- depredation.:; pc: ..eight category) ascribed to large• <br /> tract generalist predators to these aggregations of nests <br /> (Martin & Roper 1988; Schmidt &Whelan 1998). <br /> 0.07 72 ❑ thrush <br /> T ■ robin <br /> Methods Q 0.06 18 <br /> From 1992 to 1997, we studied the nesting success of M 0.05 <br /> American Robins and Wood Thrushes in the approxi- 102 <br /> mateiv 200 ha of deciduous woodlands at The '.Morton += 58 <br /> Arboretum (15 km west of Chicago, Illinois, L,'.S.A-) and 0.04 <br /> � 1e � 53 <br /> the abutting 150-ha Hidden Lake Forest Preserve(for site O 0.03 21'40 <br /> description see Schmidt and Whelan [1998]). We lo- E 2� <br /> 7.7 <br /> cared and monitored nests throughout the breeding sea- >, <br /> son by visual inspection every 2-5 days. W'e classified 0.02 <br /> successful nests as those that fledged at least one host <br /> young, determined by inspection of the nest and sur- 0.01 <br /> roundings and by the tinting of the disappearance of <br /> nestlings. Unsuccessful nests often failed due to preda- 0.0 <br /> ,ion (>9590). We ascribed predation to large mammals e9 v- e� ``Zz v5 Ott` <br /> (e.g., raccoons) when nests were physically and vio- <br /> lently disturbed (e.g., tipped over or knocked out of a <br /> tree) or when tracks, fur, scratch marks on bark, and Plant species <br /> broken branches or stems were conspicuous. We calcu- <br /> lated the daily nest mortality rate using Mavfeld's (19-5) Figure 1. Nest daily mortality rate (DMR - 1 SE) by <br /> method. We also recorded the nest shrub or tree species nest substrate for American Robin and Wood Thrush. <br /> for all nests and visually estimated nest height to the Sample sires are given above bars. • <br /> Conservation Biology <br /> Voiumc 13,No.6,December 1999 <br />