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.

Water mites from interstitial hyporheic habitats.

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.

A riffle habitat in a stream in Wellingion Country, Ontario. A riffle habitat in a shallow river in karst topography in HastingCounty, Ontario

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.

A pool habitat in astream in Halton County, Ontario

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.

A permanent pond habitat inOntario County, Ontario.

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.

A vernal temporary pool habitat in Leeds County, Ontario

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.

A littoral habitat in a mesotrophic lake in Leeds Country, Ontario A littoral habitat in a mesotrophic lake in Peterborough County, Ontario


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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