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For the last 93 years mayfly diversity has been studied at all taxonomic levels from families to populations and all spatial and temporal scales. This has resulted in the description of almost every possible pattern with regard to latitude, elevation, habitat, climate, and season. However, if the focus is on species and sampling restricted to nymphs and the spatial scale limited to drainage networks, then a single recurring pattern appears—the hump-shaped Mid-network Mayfly Maxima (MMM). Past studies have attempted to explain this hump-shaped pattern with regards to some combination of ecologic, hydrologic, climatic, anthropogenic, or historic variables. There is wide agreement that some of these variables are important to the occurrence and distribution of individual species, but there is no consensus as to what combination of these variables comprises the best general explanation of the humped-shaped pattern. Because of the lack of agreement on how to explain this recurring pattern for mayflies and an unwillingness to acknowledge it as a general feature of drainage networks, where mayflies occur, we have become stuck trying to tease out a cause and have failed to recognize that although knowing a cause is important it may not be relevant to the broader use of this information for biomonitoring, climate monitoring, habitat management, and conservation now. I believe that there is sufficient evidence that the MMM exists and occurs in almost every major drainage system and is reasonably predictable using basic attributes of drainage networks pertinent to the aquatic life stage (nymphs). Herein I will summarize pertinent studies that support this contention; reexamine some results from one of the most comprehensive recent studies that included mayfly taxa along altitudinal gradients in North America by Gill et al. (2014), as well as a test dataset from a river in western Maine, USA; comment on information needed to estimate the location of MMM in any drainage network and how the MMM can be used; and discuss how the extent of common vs. rare species affect the perceptions of the regional species pool and the MMM.
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Larval stages have been associated for all of the known species of Eurylophella in eastern North America except for E. coxalis. The larva of E. coxalis is described herein from a reared series of specimens. Adults are redescribed and eggs are described for the 1st time, as are notes on larval habitat and behavior. Association of E. coxalis completes our knowledge of the life stages of a presumed different species, Dentatella bartoni, which was previously known only from the larval stage. This larva is now determined to be the larval stage of E. coxalis. Further, characters used to diagnose Dentatella danutae have shown that this taxon is not different from what has been called D. bartoni. Thus, Dentatella bartoni (Allen) and D. danutae McCafferty are now placed as subjective junior synonyms of E. coxalis. A conservative criterion requiring that apomorphic characters be discernable in both larval and adult life stages is proposed for recognizing mayfly genera when knowledge of life stages and/or the phylogenetic nature of diagnostic characters is incomplete. Field and laboratory observations of live E. coxalis larvae show this species to be associated with cold, swift, alkaline streams containing coarse inorganic substrates with well-developed periphyton.
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"As with previous editions, this new one is intended to serve as a standard guide to the aquatic and semiaquatic insects of North America"--Preface, xi.
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New state records are provided for two recently described species of North American Acentrella Bengtsson, 1912. Acentrella nadineae McCafferty, Waltz & Webb, 2009 is newly reported from Connecticut, Massachusetts, and Minnesota, and A. rallatoma Burian & Myers, 2011 is reported from Minnesota.
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Abstract Broad-scale aquatic insect ecological studies are an important potential source of biodiversity information, though taxa lists may contain outdated names or be incompletely or incorrectly identified. We re-examined over 12 000 archived Ephemeroptera (mayfly) specimens from a large environmental assessment project (Mackenzie Valley pipeline study) in Yukon and the Northwest Territories, Canada (1971–1973) and compared the results to data from five recent (post-2000) collecting expeditions. Our goals were to update the species list for Ephemeroptera for Yukon and the Northwest Territories, and to evaluate the benefits of retaining and re-examining ecological samples to improve regional biodiversity information, particularly in isolated or inaccessible areas. The original pipeline study specimen labels reported 17 species in 25 genera for the combined Yukon and Northwest Territories samples, of which six species and 15 genera are still valid. Re-examination of specimens resulted in 45 species in 29 genera, with 14 and seven newly recorded species for Northwest Territories and Yukon, respectively. The recent collecting resulted in 50 species, 29 of which were different from the pipeline study, and five of which were new territorial records (Northwest Territories: four species; Yukon: one species). Re-examination of archived ecological specimens provides a cost-effective way to update regional biodiversity information.
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A new species Acentrella rallatoma (type locality: Connetquot River, Oakdale, NY, USA) is described from nymphs and reared adults. Additional specimens were studied from southeastern New York, southeastern New Hampshire, coastal Connecticut, and Martha's Vineyard, MA, USA. Nymphs can be separated from those of other Nearctic species by: scraper-like outer incisors of mandibles, cerci alternately banded from bases to tips, and row of robust bristle-like setae (with modified tips) on dorsal edge of femora. Male imagos can be separated from those that lack hind wings by: distinctive colour pattern of abdominal terga, and genitalia with pigmented sclerotised penes cover. Comparative analysis of A. rallatoma with other Nearctic species revealed a lack of comparative data on nymphs of its presumptive sister species A. parvula. To facilitate future studies of this group, the nymph of A. parvula is redescribed and regional differences are discussed. Abdominal colour patterns of A. parvula that vary over its range from Florida, USA to Labrador, Canada are illustrated. Problems concerning genus-level diagnostic characters for Acentrella nymphs and adults are discussed to facilitate placement of future taxa. To complement existing keys to Nearctic nymphs of Acentrella a provisional key to the known adult males is given. © 2011 Copyright Taylor and Francis Group, LLC.
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Mayflies (Ephemeroptera) were collected from 35 sites (streams and tundra ponds) across southern Nunavut in 2002-2005. Nine mayfly species were previously reported for Nunavut: Acentrella feropagus Alba-Tercedor and McCafferty, Acerpenna pygmaea (Hagen), Baetis bundyae Lehmkuhl, B. flavistriga McDunnough, B. foemina McDunnough, Diphetor hageni (Eaton) (Baetidae), Ephemerella aurivillii (Bengtsson) (Ephemerellidae), Leptophlebia nebulosa (Walker) (Leptophlebiidae), and Metretopus borealis (Eaton) (Metrotopidae). We add 7 species to this list, bringing the total to 16: Ameletus inopinatus Eaton (Ameletidae), Acentrella lapponica Bengtsson, Baetis hudsonicus Ide, B. tricaudatus Dodds, Heptagenia solitaria McDunnough (Heptageniidae), Rhithrogena jejuna Eaton (Heptageniidae), and Parameletus chelifer Bengtsson (Siphlonuridae). Based on numbers collected, the dominant mayfly family was Baetidae. Baetis bundyae was the most common mayfly collected, particularly in coastal areas, where larvae were found in permanent and temporary streams and in small or shallow tundra ponds. Larvae hatched 2-3 weeks after ice-out and developed rapidly in 2.5-4 weeks, emerging as adults by early August. All populations containing larvae that were large enough to sex showed female-biased sex ratios, suggesting parthenogenesis. A combination of freeze-tolerant eggs, good dispersal ability, and probable parthenogenesis is probably responsible for the success of Baetidae across the Arctic. © 2007 Entomological Society of Canada.
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Season-long sampling in streams and rivers produced 112 species of mayflies, which with other records totals 121 species for New Hampshire; 88 of these are new state records. Appearance of blackwing/mature larvae were used to develop statements on seasonality of species. Distinct differences were found between the faunas of southern and north-central New Hampshire, with an important factor being water temperatures through the season. A biogeographic analysis coupled with known habitat preferences reinforced the hypothesis that water temperature was a critical factor in determining species distributions in the state.
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We tested the efficacy of DNA barcodes in identifying mayfly species primarily from the northeastern United States and central Canada. We sequenced a 630-base-pair segment of the mitochondrial gene, cytochrome c oxidase 1 (COI), from 1 individual of each of 80 species to create a reference sequence profile. We used these reference sequences to identify 70 additional specimens representing 32 of the species that were in the profile. DNA barcodes correctly identified 69 of the 70 test specimens. The sole exception was an individual identified morphologically as Maccaffertium modestum that showed deep genetic divergence from other M. modestum specimens. Mean sequence divergence within species was 1%, whereas mean divergence among congeneric species was an order of magnitude greater (18%). We conclude that DNA barcoding can provide a powerful tool for mayfly species identification. © 2005 by The North American Benthological Society.
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