From:
ASSESSMENT OF SPECIES DIVERSITY IN THE MIXEDWOOD PLAINS ECOZONE
MITES
(Acari)
Ian M. Smith, Evert E. Lindquist
and Valerie Behan-Pelletier
CASE STUDY - WATER MITES
(Ian M. Smith)
HABITATS AND COMMUNITIES
Water mites form discrete communities of species based upon adaptations of post-larval
instars that specialize them to exploit particular freshwater habitats and microhabitats.
In the Mixedwood Plains, eight reasonably distinct communities can be identified in association with different habitat types. Most species are strongly associated
with one particular habitat type, but some are able to exploit a variety of similar
types (eg. rheocrene springs and riffle areas, stream pools and lakes), and consequently may be represented in more than one community. These communities are richly
polyphyletic and often represent unique assemblages of species that have different
post-glacial biogeographic histories and occur together nowhere else.
Freshwater habitats are especially vulnerable to physical disturbance and chemical
pollution. Both the quantity and quality of these habitats in the Mixedwood Plains
have been significantly degraded by agricultural, industrial, recreational and urban
development, especially in the Lake Erie Lowlands. Nearly 80% of the original 2 million
hectares of wetland habitat in the Mixedwood Plains has been eliminated or seriously
damaged by human activities. Springs and streams have been extensively dammed, diverted, channelled, silted up and polluted. Ponds and lakes have undergone progressive
eutrophication and intensive recreational exploitation. All of these activities
have had inadvertent impacts on freshwater invertebrate communities. Water mites
are useful indicators of biodiversity change in these communities because of their high taxonomic
diversity, abundance in all kinds of habitats and robust interactions with other
organisms, especially insects. In addition, water mites are relatively easy to collect and identify compared to many other groups of freshwater arthropods because the
adult instar is fully aquatic.
Springs
About 60 species representing 30 genera and 20 families inhabit springs and seepage
areas in the Mixedwood Plains. Communities from individual sites may include up
to 20 different species. Deutonymphs and adults are typically specialized for crawling
on moss mats and detritus. Most species are cold-adapted crenobionts but some (eg.
Laversia berulophila)
are more generalized stenophiles also able to live in the profundal zone of oligotrophic
lakes. Many crenophilic species are distributed widely in well drained areas of
the Boreal Shield and Atlantic-Maritime Ecozones, with scattered populations in the
Mixedwood Plains. Most of these species have Northeastern or Boreal distributions.
They probably inhabited Pleistocene refugia in discharge areas associated with highlands
near the edge of the Laurentide Ice Sheet and dispersed through the Mixedwood Plains early in the Holocene, leaving relict populations in persistent cold springs as
they moved north. Spring habitats are common throughout the Mixedwood Plains, but
they and their arthropod communities are increasingly threatened by intensive agriculture and residential development in urban areas, especially in the Lake Erie Lowlands.
Information on springs and their biota in the Mixedwood Plains Ecozone is fragmentary,
despite their importance as sources for surficial watersheds and indicators of ground water quality, respectively . Mites, insects and crustaceans are the dominant animal
groups in spring habitats. We need to develop an inventory of springs in the
Ecozone and compile a relational database on their arthropod species and communities.
This would permit development of baselines for assessing and monitoring biodiversity
change in a network of selected springs and permit correlation of documented changes with environmental stressors using Geographical Information System technology.
Groundwater/Hyporheos
Approximately 20 species representing 15 genera and 15 families inhabit subsurface
water in the Mixedwood Plains. Communities from individual sites may include up
to 10 different species. Deutonymphs and adults are typically specialized for running
through subsurface interstices in gravel deposits.
They usually lack both pigment and
functional eyes (Fig.M-44). Most of these species have Northeastern distributions and are distributed
widely in the Atlantic-Maritime Ecozone with scattered populations in the Mixedwood Plains and southern regions of the Boreal Shield Ecozone. Others have Southeastern
distributions. All of them probably inhabited Pleistocene refugia in highland and
piedmont areas remote from the edge of the Laurentide Ice Sheet and dispersed gradually into the Mixedwood Plains as stable fluvial depositional areas became reestablished
during the Holocene. These habitats apparently developed more rapidly in the Atlantic-Maritime
Ecozone as a result of its more varied topography and elevation. Subterranean freshwater habitats and their arthropod communities are being degraded in the
Mixedwood Plains, especially in agricultural and urban areas of extreme southern
Ontario, by chemical pollution, siltation and compaction. Knowledge of groundwater
biota in the Mixedwood Plains is rudimentary, but my initial surveys show that some of the
water mite species which characterize the rich phreatic communities in unglaciated
parts of North America have established populations in the Ecozone. As in the case
of spring fauna, we need to develop relational databases for these mites and initiate
monitoring in selected aquifers to document biodiversity changes and correlate them
with local environmental stressors.
Stream Riffles
About 100 species representing 22 genera and 12 families inhabit flowing
water in erosional zones of streams and rivers in the Mixedwood Plains (Fig.M-45).
Communities from individual sites may include up to 25 different
species. The dominant genera in riffle habitats are among the least
well known taxa in the Ecozone. Deutonymphs and adults of mites in
these habitats are typically specialized for clinging and crawling on
rocks and aquatic plants. Most of the species are relatively
cold-adapted stenophiles distributed widely in small streams of the
Mixedwood Plains, Atlantic-Maritime and southern regions of the Boreal
Shield Ecozone. Most of them have Southeastern or Northeastern
distributions. They probably inhabited Pleistocene refugia in
erosional areas associated with highlands such as the Ozark Plateau,
Cumberland Plateau and Appalachian Mountains south of the Laurentide
Ice Sheet, and dispersed into the Mixedwood Plains and contiguous
eastern Canadian Ecozones as lotic habitats stabilized during the
Holocene. A small group of species are relatively warm-adapted and
restricted to shallow rivers and streams in Karst areas of the
Mixedwood Plains and Atlantic-Maritime Ecozones (Fig.M-46). Several of these
species represent clades that apparently invaded North America from
South America following establishment of the Panamanian Isthmus during
the Pliocene, and have reached the northern limits of their
distributions in the Mixedwood Plains.
Stream Pools
Nearly 100 species representing 30 genera and 16 families inhabit pools in depositional
zones of streams and rivers in the Mixedwood Plains (Fig. M-47).
Communities from individual
sites may include up to 60 different species. Deutonymphs and adults are typically
specialized for swimming and burrowing in silt. Most of these species are cool-adapted
stenophiles with Northeastern or Boreal distributions, found widely in small streams
in the Mixedwood Plains, Atlantic-Maritime and Boreal Shield Ecozones. Many of themalso can also exploit sublittoral habitats in small lakes. They probably inhabited
Pleistocene refugia in depositional areas south of the Laurentide Ice Sheet and dispersed
into the Mixedwood Plains as lotic habitats stabilized during the Holocene.
Streams and their arthropod communities are being degraded by siltation caused by
erosion associated with intensive agriculture, chemical pollution and urban development
throughout the Ecozone, with the greatest impacts to date in the Lake Erie Lowland
Ecoregion. Although a substantial among of research has been done on stream biota in
the Mixedwood Plains, this has rarely resulted in well documented inventories of
arthropod species that could be used as baselines for monitoring spatial or temporal
biodiversity change. This is unfortunate, because mites, along with insects and crustaceans,
comprise most of the faunal species diversity in stream habitats. They can be used
as sensitive indicators to detect changes in community composition at an early stage, permitting action to be taken to mediate the impact of stressors before profund
and irreversible degradation of community structure occurs, with implications for
fish and other organisms at higher levels of the food chain. Here again, we need
to establish and maintain relational databases on selected taxa that can be linked to information
on regional and local stressors using GIS technology. Improving taxonomic knowledge
of the most diverse genera of rheobiontic water mites would be a necessary but cost-effective step toward this objective, because the adult mites can be more rapidly
and reliably identified than the aquatic larvae of their insect hosts.
Bog Pools
Nearly 50 species representing 17 genera and 12 families inhabit bog pools in the
Mixedwood Plains. Communities from individual sites may include up to 20 different
species. Deutonymphs and adults are typically specialized for clinging to Sphagnum
and swimming. Most of these species are cool-adapted halophiles with Northeastern or Boreal
distributions and with scattered populations in relict bogs in the Mixedwood Plains.
They probably inhabited tundra pools in periglacial Pleistocene refugia and dispersed through the Mixedwood Plains early in the Holocene leaving relict populations
in poorly drained areas as they moved northward.
Bogs and their arthropod communities in the Mixedwood Plains are being degraded by
wetland drainage programs and associated agricultural and urban development. Bog
communities contain some highly specialized mites that are rare in the Ecozone.
The taxonomy of bog- dependent water mite species is sufficiently well known to permit development
of a relational database for this fauna. It would be useful to establish baselines
for species populations and community composition at selected bog sites, and to monitor for spatial and temporal changes along a transect extending northward to include
some relatively large and undisturbed bogs in the Boreal Shield Ecozone.
Ponds/Marshes
Over 100 species representing 17 genera and 12 families inhabit ponds and marshes
in the Mixedwood Plains (Fig.M-48).
Communities from individual sites may include as many as
50 different species. Deutonymphs and adults are typically specialized for swimming
and clinging to plants. Most of these species exhibit broad temperature tolerance, and
some have extensive Northeastern or Boreal distributions. Others, notably certain
species of the genus Arrenurus,
appear to have limited distributions within the Great Lakes Basin. A number of
the species in this group also exploit shallow, littoral habitats in small eutrophic
and mesotrophic lakes. They probably inhabited Pleistocene refugia remote from the
edge of the Laurentide Ice Sheet and dispersed gradually into the Mixedwood Plains during
the Holocene.
Mites and associated arthropod communities that depend on ponds and marshes have been
greatly reduced in the Mixedwood Plains by wetland drainage programs associated with
agricultural, urban and industrial development. Large areas of many formerly extensive marshes have been drained and filled, and populations of mite species and their
host insects have been fragmented and isolated in small remnant patches of habitat.
Some of these species are endemic to the Great Lakes Basin and still occur most
commonly and abundantly in the Mixedwood Plains Ecozone. Developing a relational database
for these mites would permit us to monitor their populations as indicators of the
sustainability of arthropod communities in critical wetland habitats.
Vernal Temporary Pools
About 60 species representing 14 genera and 8 families inhabit vernal temporary pools
in the Mixedwood Plains (Fig.M-49).
Communities from individual sites may include up to 20
different species. Deutonymphs and adults are typically specialized for clinging
to plants and detritus or swimming. All of these species exhibit adaptations for either
avoiding or withstanding drought that characteristically extends from early summer
until the following spring. Most of them exhibit exceptionally broad temperature
tolerance and are distributed widely in the Mixedwood Plains, Atlantic-Maritime and Boreal
Shield Ecozones. Many of the species in this group have Northeastern or Boreal distributions;
some others are known only from the Great Lakes Basin. A few species are halophiles restricted to intermittent pools in fens and bogs, with distributions that
may extend to the high Arctic. Mites able to exploit temporary vernal pools probably
inhabited seasonally intermittent tundra pools in periglacial Pleistocene refugia,
in regions with marked spring melting and summer drought. They apparently dispersed through
the Mixedwood Plains early in the Holocene, leaving relict populations in areas with
perched water tables as they moved further north.
Vernal temporary pools are common in the Mixedwood Plains Ecozone, but are often disregarded
as significant habitats because they are seasonal. They are frequently filled or
drained to reduce mosquito populations and permit agricultural or residential development. In fact, many insects breed only in temporary pools, and the water mites
associated with them occur exclusively in these habitats (Wiggins et al. 1980). Developing
a relational database for these species would permit monitoring of populations of
mosquitoes and their parasites at selected sites, and would provide insight on dispersal
of these species and other members of this fascinating arthropod community.
Lakes
About 200 species representing 30 genera and 20 families inhabit lakes in the Mixedwood
Plains. Communities from certain mesotrophic lakes (Fig.M-50, Fig.M-51) comprise exceptional diversity
and may include up to 100 different species.
Swarms of 20 or more species in each of the genera Arrenurus and Piona
may live sympatrically in some of these lakes. Deutonymphs and adults of mites inhabiting
lakes are typically specialized for swimming or clinging to plants. Lake inhabiting
water mites of the Mixedwood Plains exhibit a remarkable diversity of post-glacial origins and dispersals, and illustrate all major distribution patterns. Various
species also occur in shallow lakes in the eastern United States, the Atlantic-Maritime
Ecozone or Boreal Shield Ecozone, and a few have very broad distributions extending westward to the Prairie Ecozone and beyond. The Mixedwood Plains represent a biogeographic
crossroads for these mites, and many of the species assemblages that characterize
mesotrophic lake communities in this Ecozone occur nowhere else.
Mesotrophic lakes, with their unique water
mite assemblages and arthropod communities, are distributed throughout the Mixedwood
Plains, especially in the Manitoulin-Lake Simcoe Ecoregion from the Rideau Waterway
to the Kawartha Lakes and into the Bruce Peninsula. They are increasingly threatened
with physical and biological degradation by agricultural, recreational and urban
development. Changes in the species diversity of arthropod taxa and communities
in these lakes provide early signals of degenerative trends that may ultimately result in irreversible
damage to the integrity of aquatic ecosystems. Development of relational databases
for selected groups of these mites and their insect hosts would permit monitoring of species populations and community composition. Monitoring should be conducted
at a series of sites arranged along longitudinal and latitudinal transects traversing
the Ecozone to detect and characterize both spatial and temporal changes, and should
incorporate GIS capabilities to provide the basis for correlating changes with environmental
stressors and interpreting their significance.
About 20 species representing 15 genera and 10 families are restricted to profundal
substrata in oligotrophic lakes in the Mixedwood Plains. Communities in this habitat
are relatively depauperate, and usually contain about 10 species. Deutonymphs and
adults are typically specialized for swimming and burrowing in silt. These species
(eg. the pionid Huitfeldtia rectipes
Thor and the arrenurid Arrenurus serratus
Marshall) are cold-adapted stenophiles with extensive Boreal distributions that may
extend into Arctic Ecoregions. They probably inhabited Pleistocene ice-front lakes
in refugia near the edge of the Laurentide Ice Sheet and dispersed through the Mixedwood Plains early in the Holocene leaving relict populations in deep lakes as they moved
northward.
Oligotrophic lakes, including the Great Lakes, have been subject to accelerating pollution
and eutrophication throughout the historic period of human activity in the Mixedwood
Plains. Physical changes have had profound impact on the species and communities inhabiting these lakes, as have intensive fish harvesting and the introduction
of invasive exotic species. The benthic profundal fauna of mites and other arthropods
represents a relatively small and taxonomically well known resident community that
is not targeted by humans for direct manipulation. Monitoring of the species composition
of this community in selected lakes would, therefore, provide a clear indication
of the impact of physical changes on biodiversity. Most of the members of this community are cold-adapted species with either Boreal or Arctic distributions, and the status
of their relict populations in the Mixedwood Plains would also be a useful indicator
of the impact of increasing water temperature on lake biota in the Ecozone.
TABLE 6: LIST OF NAMED SPECIES OF WATER MITES IDENTIFIED
FROM THE MIXEDWOOD PLAINS ECOZONE
(Unnamed species included are only known representative of genus in Ecozone)
Superfamily - Hydrovolzoidea
Family - Hydrovolziidae
Hydrovolzia mitchelli Habeeb
Superfamily - Eylaoidea
Family - Limnocharidae
Limnochares americana Lundblad
Limnochares aquatica (Linnaeus)
Neolimnochares n. sp.
Rhyncholimnochares kittatiniana Habeeb
Family - Piersigiidae
Piersigia limnophila Protz
Family - Eylaidae
Eylais deviata Smith
Eylais discreta Koenike
Eylais euryhalina Smith
Eylais infundibulifera Koenike
Eylais lancianii Smith
Eylais wainsteini Smith
Superfamily - Hydrachnoidea
Family - Hydrachnidae
Hydrachna baculoscutata Crowell
Hydrachna barri Smith
Hydrachna canadensis Marshall
Hydrachna crenulata Marhall
Hydrachna cruenta Muller
Hydrachna davidsi Smith
Hydrachna elongata Smith
Hydrachna hesperia Lundblad
Hydrachna hungerfordi Lundblad
Hydrachna hutchinsoni Smith
Hydrachna magniscutata Marshall
Hydrachna marshallae Lundblad
Hydrachna milaria Berlese
Hydrachna rotunda Marshall
Hydrachna severnensis Smith
Hydrachna stipata Lundbald
Superfamily - Hydryphantoidea
Family - Hydryphantidae
Hydryphantes multiporus Marshall
Hydryphantes ruber (de Geer)
Hydryphantes tenuabilis Marshall
Thyasides sphagnorum Habeeb
Thyas barbigera (de Geer)
Thyas inepta Lundblad
Thyas rivalis Koenike
Thyas stolli Koenike
Zschokkea bruzelii Lundblad
Euthyas mitchelli Cook
Euthyas truncata (Neuman)
Trichothyas muscicola (Mitchell)
Thyopsella dictyophora Cook
Thyopsis cancellata (Protz)
Panisopsis asopos (Cook)
Panisopsis gorhami (Habeeb)
Panisopsis setipes (Viets)
Panisus cataphractus (Koenike)
Panisus condensatus Habeeb
Peudohydryphantes latipalpus Marshall
Wandesia gaspensis Habeeb
Family - Hydrodromidae
Hydrodroma despiciens (Muller)
Family - Rhynchohydracaridae
Clathrosperchon americanus Habeeb
Superfamily - Lebertioidea
Family - Sperchontidae
Sperchon decorellus Habeeb
Sperchon glandulosus Koenike
Sperchon mitchelli Habeeb
Sperchonopsis iansmithi Conroy
Sperchonopsis latipalpis Conroy
Sperchonopsis magniscuta Conroy
Sperchonopsis ovalis Marshall
Sperchonopsis protuberosa Conroy
Sperchonopsis tuberculata Conroy
Family - Teutoniidae
Teutonia setifera Habeeb
Family - Anisitsiellidae
Bandakia borealis Smith
Bandakia phreatica Cook
Bandakia vietsi Cook
Family - Lebertiidae
Lebertia annae Habeeb
Lebertia danieli Habeeb
Lebertia ontarioensis Marshall
Lebertia porosa Thor
Lebertia pushorum Habeeb
Lebertia quinquemaculosa Marshall
Family - Oxidae
Frontipoda americana Marshall
Oxus auburnensis Habeeb
Oxus connatus Marshall
Oxus deceptor Habeeb
Oxus elongatus Marshall
Oxus gnaphiscoides Habeeb
Oxus intermedius Marshall
Family - Torrenticolidae
Testudacarus vulgaris Habeeb
Torrenticola bittikoferae Crowell
Torrenticola jordanensis Marshall
Torrenticola neoanomala Habeeb
Superfamily - Hygrobatoidea
Family - Limnesiidae
Limnesia americana Piersig
Limnesia anomala Koenike
Limnesia cornuta Wolcott
Limnesia eggletoni Cook
Limnesia fulgida Koch
Limnesia marshallae (Viets)
Limnesia marshalliana Lundblad
Limnesia paucispina Wolcott
Limnesia undulata (Muller)
Limnesia wawaseea Marshall
Tyrrellia circularis Koenike
Tyrrellia ovalis Marshall
Family - Hygrobatidae
Atractides parviscutatus Marshall
Atractides nodipalpis Thor
Hygrobates canadensis Habeeb
Hygrobates longipalpis (Hermann)
Hygrobates multiporus Koenike
Hygrobates neocalliger Habeeb
Hygrobates neooctoporus Marshall
Family - Feltriidae
Feltria amoenella Habeeb
Feltria cornuta Walter
Feltria geometrica Habeeb
Feltria minuta Koenike
Feltria purpurotincta Habeeb
Feltria rivophila Habeeb
Family - Unionicolidae
Neumania brucei Conroy
Neumania canoga Habeeb
Neumania distincta Marshall
Neumania extendens Marshall
Neumania fragilis Marshall
Neumania hickmani Marshall
Neumania ovata Marshall
Neumania papillator Marshall
Neumania pubescens Marshall
Neumania punctata Marshall
Neumania semicircularis Marshall
Neumania setosipalpa Conroy
Neumania tenuipalpis Marshall
Koenikea aphrasta Cook
Koenikea concava Wolcott
Koenikea haldemani Viets
Koenikea smithi Cook
Koenikea spinipes (Wolcott)
Koenikea wolcotti Viets
Unionicola abnormipes (Wolcott)
Unionicola arcuata (Wolcott)
Unionicola campelomaicola Marshall
Unionicola crassipes Muller
Unionicola pectinata (Wolcott)
Unionicola serrata (Wolcott)
Unionicola ypsilophora (Bonz)
Family - Pionidae
Wettina octopora Cook
Wettina ontario Smith
Hydrochoreutes michiganensis Cook
Hydrochoreutes microporus Cook
Hydrochoreutes schizopetiolatus Cook
Pseudofeltria multipora Cook
Forelia americana Cook
Forelia borealis (Habeeb)
Forelia cayuga Habeeb
Forelia cursor Habeeb
Forelia onondaga Habeeb
Forelia ovalis Marshall
Forelia pinguipalpis Smith
Forelia siegasiana Habeeb
Huitfeldtia rectipes Thor
Neotiphys pionoidellus (Habeeb)
Pionopsis paludis Habeeb
Tiphys americanus (Marshall)
Tiphys brevipes Habeeb
Tiphys cooki Smith
Tiphys diversus (Marshall)
Tiphys marshallae Cook
Tiphys mitchelli Cook
Tiphys ornatus Koch
Tiphys scaurus (Koenike)
Tiphys vernalis (Habeeb)
Najadicola ingens (Koenike)
Nautarachna muskoka Smith
Nautarachna queticoensis Smith
Piona americana Marshall
Piona brunsoni Cook
Piona carnea (Koch)
Piona clavicornis (Muller)
Piona conglobata (Koch)
Piona constricta (Wolcott)
Piona coronis (Wolcott)
Piona crassa (Wolcott)
Piona debilis (Wolcott)
Piona exilis (Wolcott)
Piona inconstans (Wolcott)
Piona interrupta Marshall
Piona michiganensis Cook
Piona mitchelli Cook
Piona napio Crowell
Piona neumani (Koenike)
Piona pugilis (Wolcott)
Piona rotunda (Kramer)
Piona spinulosa (Wolcott)
Piona turgida (Wolcott)
Piona uncata (Koenike)
Piona variabilis (Koch)
Piona wolcotti Marshall
Family - Aturidae
Ljania bipapillata Thor
Ljania michiganensis Cook
Axonopsis setoniensis Habeeb
Brachypoda cornipes Habeeb
Brachypoda setosicauda Habeeb
Woolastookia pilositarsa Habeeb
Albia caerulea Marshall
Albia neogaea Habeeb
Aturus deceptor Habeeb
Aturus mirabilis Piersig
Kongsbergia paterna Habeeb
Kongsbergia semiornata Habeeb
Superfamily - Arrenuroidea
Family - Momoniidae
Momonia campylotibia Smith
Stygomomonia riparia Habeeb
Family - Nudomideopsidae
Nudomideopsis magnacetabula (Smith)
Family - Mideidae
Midea expansa Marshall
Family - Mideopsidae
Mideopsis (sensu stricto) americana Marshall
Mideopsis (s. s.) borealis Habeeb
Mideopsis (s. s.) fibrosa Lundblad
Mideopsis (s. s.) gladiator Habeeb
Mideopsis (s. s.) crassipes Soar
Mideopsis (s. s.) lamellipalpis Lundblad
Mideopsis (s. s.) marshallae Cook
Mideopsis (Xystonotus) aspera (Wolcott)
Mideopsis (Xyst.) delicata (Habeeb)
Mideopsis (Xyst.) interstitialis Cook
Mideopsis (Xyst.) robusta (Habeeb)
Mideopsis (Xyst.) wolcotti Cook
Family - Chappuisididae
Uchidastygacarus acadiensis Smith
Family - Athienemanniidae
Chelomideopsis besselingi (Cook)
Stygameracarus canadensis Smith
Family - Acalyptonotidae
Paenecalyptonotus fontinalis Smith
Family - Neoacaridae
Neoacarus lacus Smith
Neoacarus motasi Cook
Neoacarus similis Cook
Volsellacarus n. sp.
Family - Laversiidae
Laversia berulophila Cook
Family - Krendowskiidae
Geayia ontario Smith
Geayia ovata (Wolcott)
Krendowskia similis Viets
Family - Arrenuridae
Arrenurus (Truncaturus) acuminatus Mullen
Arrenurus (Trunc.) angustilimbatus Mullen
Arrenurus (Trunc.) danbyensis Mullen
Arrenurus (Trunc.) kenki Marshall
Arrenurus (Trunc.) lacrimatus Cook
Arrenurus (Trunc.) palustris Mullen
Arrenurus (Trunc.) ringwoodi Mullen
Arrenurus (Trunc.) rufopyriformis Habeeb
Arrenurus (Micruracarus) acutus Marshall
Arrenurus (Micr.) bicaudatus Marshall
Arrenurus (Micr.) cheboyganensis Cook
Arrenurus (Micr.) crenellatus Marshall
Arrenurus (Micr.) hiatocaudatus Cook
Arrenurus (Micr.) infundibularis Marshall
Arrenurus (Micr.) laticaudatus Marshall
Arrenurus (Micr.) lyriger Marshall
Arrenurus (Micr.) ovalis Marshall
Arrenurus (Micr.) pseudosetiger Marshall
Arrenurus (Micr.) scutulatus Marshall
Arrenurus (Micr.) setiger Koenike
Arrenurus (Megaluracarus) alticorpus Wilson
Arrenurus (Meg.) apetiolatus Piersig
Arrenurus (Meg.) bartonensis Cook
Arrenurus (Meg.) birgei Marshall
Arrenurus (Meg.) cardiacus Marshall
Arrenurus (Meg.) dinotoformis Cook
Arrenurus (Meg.) elevatus Marshall
Arrenurus (Meg.) intermedius Marshall
Arrenurus (Meg.) longicaudatus Marshall
Arrenurus (Megaluracarus) mamillanus Marshall
Arrenurus (Meg.) manubriator Marshall
Arrenurus (Meg.) marshallae Piersig
Arrenurus (Meg.) megalurus Marshall
Arrenurus (Meg.) neobirgei Cook
Arrenurus (Meg.) neomamillanus Cook
Arrenurus (Meg.) opisthifoliacercus Young
Arrenurus (Meg.) pseudaphelocercus Wilson
Arrenurus (Meg.) pseudocaudatus Marshall
Arrenurus (Meg.) pseudoconicus Piersig
Arrenurus (Meg.) pseudocylindratus Piersig
Arrenurus (Meg.) pseudotenuicollis Wilson
Arrenurus (Meg.) rawsoni Marshall
Arrenurus (Meg.) rectangularis Marshall
Arrenurus (Meg.) rotundus Marshall
Arrenurus (Meg.) scutuliformis Marshall
Arrenurus (Meg.) semicircularis Marshall
Arrenurus (Meg.) siegasianus Habeeb
Arrenurus (Meg.) solifer Marshall
Arrenurus (Meg.) unisinuatus Wilson
Arrenurus (Meg.) wardi Marshall
Arrenurus (sensu stricto) americanus Marshall
Arrenurus (s. s.) amplus Marshall
Arrenurus (s. s.) bleptopetiolatus Cook
Arrenurus (s. s.) compactilis Marshall
Arrenurus (s. s.) dentipetiolatus Marshall
Arrenurus (s. s.) drepanophorus Cook
Arrenurus (s. s.) falcicornis Marshall
Arrenurus (s. s.) fissicorniformis Cook
Arrenurus (s. s.) fissicornis Marshall
Arrenurus (s. s.) flabellifer Marshall
Arrenurus (s. s.) gennadus Cook
Arrenurus (s. s.) hungerfordi Cook
Arrenurus (s. s.) laticornis Marshall
Arrenurus (s. s.) magnicaudatus Marshall
Arrenurus (s. s.) major Marshall
Arrenurus (s. s.) mucronatus Lavers
Arrenurus (s. s.) paracascadensis Conroy
Arrenurus (s. s.) pinguisomus Cook
Arrenurus (s. s.) planus Marshall
Arrenurus (s. s.) pleopetiolatus Marshall
Arrenurus (s. s.) pollictus Marshall
Arrenurus (s. s.) pseudosuperior Cook
Arrenurus (s. s.) reflexus Marshall
Arrenurus (s. s.) serratus Marshall
Arrenurus (s. s.) superior Marshall
Arrenurus (s. s.) tetratumuli Munchberg
Arrenurus (s. s.) trifoliatus Marshall
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