DNA metabarcoding reveals broadly overlapping diets in three sympatric North American hummingbirds

Author(s):  
Austin R Spence ◽  
Erin E Wilson Rankin ◽  
Morgan W Tingley

ABSTRACT Hummingbirds, a highly diverse avian family, are specialized vertebrate pollinators that feed upon carbohydrate-rich nectar to fuel their fast metabolism while consuming invertebrates to obtain protein. Previous work has found that morphologically diverse hummingbird communities exhibit higher diet specialization on floral resources than morphologically similar hummingbird communities. Due to the difficulties of studying avian diets, we have little understanding whether hummingbirds show similar patterns with their invertebrate prey. Here, we use DNA metabarcoding to analyze floral and invertebrate diets of 3 species of sympatric North American hummingbirds. We collected fecal samples from 89 Anna’s (Calypte anna), 39 Black-chinned (Archilochus alexandri), and 29 Calliope (Selasphorus calliope) hummingbirds in urban and rural localities as well as across an elevational gradient from sea level to 2,500 meters above sea level in California, USA. We found hummingbirds showed high dietary overlap in both invertebrate and plant resources, with few invertebrate and plant families common to most individuals and many families found in only a few individuals. Chironomidae was the most common invertebrate family across all species, and Rosaceae and Orobanchaceae were the most common plant families. Anna’s Hummingbirds had significantly higher invertebrate diet diversity than Black-chinned Hummingbirds when found at the same sites, but we found no difference in plant diet diversity among any of the 3 species. Hummingbirds in urban sites had higher plant diet diversity than in rural sites, but we found no effect of elevation on dietary richness. Our study shows how DNA metabarcoding can be used to non-invasively investigate previously unknown life-histories of well-studied birds, lending insight to community structure, function, and evolution.

1899 ◽  
Vol 8 (281) ◽  
pp. 407-408 ◽  
Author(s):  
Harrison G. Dyar

1901 ◽  
Vol 9 (303) ◽  
pp. 226-227 ◽  
Author(s):  
Harrison G. Dyar

1900 ◽  
Vol 9 (285) ◽  
pp. 9-10 ◽  
Author(s):  
Harrison G. Dyar

1899 ◽  
Vol 8 (273) ◽  
pp. 310-311 ◽  
Author(s):  
Harrison G. Dyar

1964 ◽  
Vol 71 (1) ◽  
pp. 251
Author(s):  
R. E. Gordon ◽  
A. C. Bent

2000 ◽  
Vol 74 (3) ◽  
pp. 444-463 ◽  
Author(s):  
Xueping Ma ◽  
Jed Day

The cyrtospiriferid brachiopod genus Tenticospirifer Tien, 1938, is revised based on restudy of the type species from the Frasnian (Late Devonian) of the Russian Platform. As revised the genus includes cyrtospiriferid species with pyramidal ventral valves, catacline ventral interareas, a narrow delthyrium, few sinal plications, and lack a median dorsal septum and pseudodeltidium. All species retained in the genus are of Givetian and Frasnian age. All Famennian age species described from South China and North America are rejected from the genus. It appears that Tenticospirifer evolved during the early Givetian in western Europe and remained endemic to that region during the remainder of the Givetian. Successive migrations of Tenticospirifer from eastern Laurussia to North America, then to South China and possibly Australia, coincided with middle and late Frasnian eustatic sea level rises, respectively. The North American species Spirifera cyrtinaformis Hall and Whitfield, 1872, and related species identified as Tenticospirifer by North American workers, are reassigned to Conispirifer Lyashenko, 1985. Its immigration to and widespread dispersal in carbonate platforms of western Laurussia, northern Gondwana and tropical island arcs (?) coincided with a major late Frasnian eustatic sea level rise. The new family Conispiriferidae is proposed with Conispirifer Lyashenko, 1985, selected as the type genus. The new family also includes the new genus Pyramidaspirifer with Platyrachella alta Fenton and Fenton, 1924, proposed as the type species. The affinity of the new family remains uncertain pending restudy of key genera currently included in the Superfamily Cyrtospiriferoidea. Available data from the Devonian brachiopod literature indicate that species of Pyramidaspirifer are restricted to late Frasnian deposits of central and western North America.


Ecosphere ◽  
2020 ◽  
Vol 11 (4) ◽  
Author(s):  
Douglas B. Sponsler ◽  
Don Shump ◽  
Rodney T. Richardson ◽  
Christina M. Grozinger

1992 ◽  
Vol 6 ◽  
pp. 149-149
Author(s):  
Jisuo Jin

Three rhynchonellid brachiopod genera, Hiscobeccus, Lepidocyclus, and Hypsiptycha, are the most diagnostic elements of the Lepidocyclus fauna of North America in Late Ordovician time. These are characterized by relatively large, strongly biconvex to globular shells with coarse imbricating growth lamellae and, internally, with septiform cardinal processes in brachial valves. Among the three genera, Hiscobeccus appears the earliest, now known from rocks of late Trentonian-Edenian age in the Canadian Rocky Mountains and Mackenzie Mountains. Morphologically, Hiscobeccus is distinguished from the other two genera by its open delthyrium in the pedicle valve. Early forms of Hiscobeccus show close morphological similarity to Rhynchotrema in their non-globular biconvex shells covered by strong growth lamellae only in the anterior portions. It has been suggested that Hiscobeccus evolved from the Rhynchotrema wisconsinense stock through increase in shell size, globosity, and strength of growth lamellae. Earliest species of Rhynchotrema has been documented convincingly from rocks of early Trentonian age, and the derivation of Hiscobeccus most likely took place during the mid-Trentonian. Lepidocyclus and Hypsiptycha evolved from either Rhynchotrema or Hiscobeccus by developing a pair of deltidial plates covering the delthyrium.Rhynchotrema and other rhynchonellids that evolved before mid-Trentonian time are common to the North American (Laurentian) and the Siberia-Kazakhstan paleocontinents. In contrast, Hiscobeccus, Lepidocyclus, and Hypsiptycha that evolved after the mid-Trentonian are virtually restricted to Laurentia. Therefore, Rhynchotrema marked the last successful intercontinental migration of rhynchonellids during their Llandeilian-Caradocian cosmopolitanism. The pronounced provincialism of the North American Lepidocyclus fauna may have been caused by a number of factors. Facies control is not likely the explanation because these rhynchonellids occur in nearly all the inland and marginal platform seas of Laurentia and commonly are found together in the same types of rocks. Plate tectonics and sea-level changes are considered major causes. The Ordovician rhynchonellids lived in shallow marine (intertidal-subtidal) environments and were incapable of crossing vast, deep oceanic barriers because of their sedentary mode of life and short-lived motile larval stages. The widening of the ocean between North America and Siberia, coupled with high sea-level stand, may have created a sufficiently wide oceanic barrier to interrupt faunal mixing between the two paleocontinents by late Trentonian time. Moreover, the rise in sea level would have resulted in the disappearance of island faunas, which could have served as stepping stones for intercontinental migration of shallow-water benthic faunas during low sea-level stand.


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