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Complex responses within a desert bee guild (Hymenoptera: Apiformes) to urban habitat fragmentation

Publication Name Ecological Applications
Data Source Ecological Applications
Data Type Publication
Volume 16
Journal Number 2
Publication Year 2006
Publication Place
Publisher
Pagination pp. 632-644
ISBN/ISSN
Robert L. Minckley, Linda J. Kervin, T'ai H. Roulston, Neal M. Williams

Urbanization within the Tucson Basin of Arizona during the past 50+ years has fragmented the original desert scrub into patches of different sizes and ages. These remnant patches and the surrounding desert are dominated by Larrea tridentata (creosote bush), a long-lived shrub whose flowers are visited by >120 native bee species across its range. Twenty-one of these bee species restrict their pollen foraging to L. tridentata. To evaluate the response of this bee fauna to fragmentation, we compared species incidence and abundance patterns for the bee guild visiting L. tridentata at 59 habitat fragments of known size (0.002–5 ha) and age (up to 70 years), and in adjacent desert.
The 62 bee species caught during this study responded to fragmentation heterogeneously and not in direct relation to their abundance or incidence in undisturbed desert. Few species found outside the city were entirely absent from urban fragments. Species of ground-nesting L. tridentata specialists were underrepresented in smaller fragments and less abundant in the smaller and older fragments. In contrast, cavity-nesting bees (including one L. tridentate specialist) were overrepresented in the habitat fragments, probably due to enhanced nesting opportunities available in the urban matrix. Small-bodied bee species were no more likely than larger bodied species to be absent from the smaller fragments. The introduced European honey bee, Apis mellifera, was a minor faunal element at >90% of the fragments and exerted little if any influence on the response of native bee species to fragmentation. Overall, bee response to urban habitat fragmentation was best predicted by ecological traits associated with nesting and dietary breadth. Had species been treated as individual units in the analyses, or pooled together into one analysis, these response patterns may not have been apparent. Pollination interactions with this floral host are probably not adversely affected in this system because of its longevity and ability to attract diverse pollinators but will demand careful further study to understand.

Apiformes
biodiversity
body size
conservation
habitat fragmentation
matrix effects
nesting biology
oligolecty
pollen specialization
Tucson
Arizona
Ancylandrena larreae Larrea tridentata (creosote bush)
Perdita punctulata Larrea tridentata (creosote bush)
Perdita triangulifera Larrea tridentata (creosote bush)
Anthophora californica Larrea tridentata (creosote bush)
Anthophora vannigera Larrea tridentata (creosote bush)
Apis mellifera Larrea tridentata (creosote bush)
Centris cockerelli Larrea tridentata (creosote bush)
Centris hoffmanseggiae Larrea tridentata (creosote bush)
Centris Larrea tridentata (creosote bush)
Ceratina apacheorum Larrea tridentata (creosote bush)
Ceratina nanula Larrea tridentata (creosote bush)
Diadasia rinconis Larrea tridentata (creosote bush)
Epeolus Larrea tridentata (creosote bush)
Epeolus mesillae Larrea tridentata (creosote bush)
Ericrocis lata Larrea tridentata (creosote bush)
Melissodes Larrea tridentata (creosote bush)
Melissodes tristis Larrea tridentata (creosote bush)
Nomada Larrea tridentata (creosote bush)
Eucera conformis Larrea tridentata (creosote bush)
Townsendiella pulchra Larrea tridentata (creosote bush)
Triepeolus Larrea tridentata (creosote bush)
Xylocopa californica Larrea tridentata (creosote bush)
Xylocopa varipuncta Larrea tridentata (creosote bush)
Colletes cercidii Larrea tridentata (creosote bush)
Colletes clypeonitens Larrea tridentata (creosote bush)
Colletes covilleae Larrea tridentata (creosote bush)
Colletes louisae Larrea tridentata (creosote bush)
Colletes salicicola Larrea tridentata (creosote bush)
Colletes wootoni Larrea tridentata (creosote bush)
Hylaeus Larrea tridentata (creosote bush)
Agapostemon angelicus Larrea tridentata (creosote bush)
Agapostemon melliventris Larrea tridentata (creosote bush)
Agapostemon virescens Larrea tridentata (creosote bush)
Evylaeus amicus Larrea tridentata (creosote bush)
Lasioglossum Larrea tridentata (creosote bush)
Lasioglossum sisymbrii Larrea tridentata (creosote bush)
Nomia tetrazonata Larrea tridentata (creosote bush)
Anthidiellum ehrhornii Larrea tridentata (creosote bush)
Anthidium cockerelli Larrea tridentata (creosote bush)
Ashmeadiella cactorum Larrea tridentata (creosote bush)
Ashmeadiella parkinsoniae Larrea tridentata (creosote bush)
Ashmeadiella prosopidis Larrea tridentata (creosote bush)
Coelioxys hirsutissima Larrea tridentata (creosote bush)
Coelioxys novomexicana Larrea tridentata (creosote bush)
Dolichostelis perparvum Larrea tridentata (creosote bush)
Hoplitis biscutellae Larrea tridentata (creosote bush)
Lithurge apicalis Larrea tridentata (creosote bush)
Megachile chilopsidis Larrea tridentata (creosote bush)
Megachile discorhina Larrea tridentata (creosote bush)
Megachile lippiae Larrea tridentata (creosote bush)
Megachile newberryae Larrea tridentata (creosote bush)
Megachile odontostoma Larrea tridentata (creosote bush)
Megachile prosopodis Larrea tridentata (creosote bush)
Megachile redlandica Larrea tridentata (creosote bush)
Megachile Larrea tridentata (creosote bush)
Osmia Larrea tridentata (creosote bush)
Trachusa larreae Larrea tridentata (creosote bush)
Hesperapis larreae Larrea tridentata (creosote bush)