Anodonta nuttalliana

I. Lea, 1838

Winged Floater

G2Imperiled (G2G3Q) Found in 5 roadless areas NatureServe Explorer →
G2ImperiledGlobal Rank
VulnerableIUCN
MediumThreat Impact
Identity
Unique IDELEMENT_GLOBAL.2.108236
Element CodeIMBIV04100
Record TypeSPECIES
ClassificationSpecies
Classification StatusStandard
Name CategoryInvertebrate Animal
IUCNVulnerable
Endemicoccurs (regularly, as a native taxon) in multiple nations
KingdomAnimalia
PhylumMollusca
ClassBivalvia
OrderUnionoida
FamilyUnionidae
GenusAnodonta
Synonyms
Anodonta wahlametensisI. Lea, 1838
Other Common Names
Anodonte ailée (FR)
Concept Reference
Turgeon, D. D., J. F. Quinn, Jr., A. E. Bogan, E. V. Coan, F. G. Hochberg, W. G. Lyons, P. M. Mikkelsen, R. J. Neves, C. F. E. Roper, G. Rosenberg, B. Roth, A. Scheltema, F. G. Thompson, M. Vecchione, and J. D. Williams. 1998. Common and scientific names of aquatic invertebrates from the United States and Canada: Mollusks. 2nd Edition. American Fisheries Society Special Publication 26, Bethesda, Maryland. 526 pp.
Taxonomic Comments
Considerable taxonomic confusion surrounds this species complex. Williams et al. (2017) retain Anodonta californiensis, A. kennerlyi, A. nuttalliana, and A. oregonensis based on their phylogenetic affinity to Eurasian Anodonta (Mock et al. 2004, Zanatta et al. 2007, Chong et al. 2008). O'Brien et al. (2019) supports the distinctiveness of A. nuttalliana and A. californiensis.

Isaac Lea (1838) described Anodonta wahlametensis, Anodonta nuttalliana, and Anodonta oregonensis from the same site ("Wahlamet [Willamette River], near its junction with the Columbia River [Oregon]") all in the same publication. Call (1884) considered Anodonta nuttalliana to include, as synonyms, Anodonta wahlametensis, Anodonta oregonensis, and Anodonta californiensis. Recent authors (e.g., Burch, 1975, Clarke, 1981; Turgeon et al., 1998), however, have considered A. californiensis, A. nuttalliana, and A. oregonensis to be distinct. Some authors even continue to recognize Anodonta wahlamatensis as a distinct species (Frest and Johannes, 1995; Taylor, 1981; Henderson, 1929) while most place it in the synonymy of A. nuttaliana (Burch, 1975; Turgeon et al., 1998). Whether A. wahlamatensis should be removed from the synonymy of A. nuttalliana will depend on future anatomical and genetic work on western Anodonta.

Mock et al. (2004; 2005) found a lack of resolution (very little nuclear diversity) in phylogenetic reconstructions of Anodonta (A. californiensis, A. oregonensis, A. wahlamatensis) populations in the Bonneville Basin, Utah, but there was a tendency for the Bonneville Basin Anodonta (tentatively A. californiensis) to cluster with A. oregonensis from the adjacent Lahontan Basin in Nevada. Zanatta et al. (2007) supported the monophyly of both Pyganodon and Utterbackia using mutation coding of allozyme data, but also resolved the Eurasian Anodonta cygnea to Pyganodon, Utterbackia, and North American Anodonta; indicating futher phylogenetic analysis of the Anodontinae is required including both North American and Eurasian species. In a phylogenetic analysis of western North American Anodonta using topotypic material as was available, Chong et al. (2008) found three deeply divided lineages: one clade including Anodonta oregonensis and Anodonta kennerlyi, one clade including Anodonta californiensis and Anodonta nuttalliana, and one clade including Anodonta beringiana. A. californiensis is likely to be synonymized with nuttalliana in the near future.
Conservation Status
Rank MethodLegacy Rank calculation - Excel v3.1x
Review Date2018-12-06
Change Date2018-12-06
Edition Date2018-12-06
Edition AuthorsHeinold, B.
Threat ImpactMedium
Range Extent200,000-2,500,000 square km (about 80,000-1,000,000 square miles)
Number of Occurrences21 - 80
Rank Reasons
Documented long- and short-term declines in A. nuttalliana and other western Anodonta species since last review in 2009. Low genetic diversity with hydrologic separation between populations. Distribution, along with species designation, is poorly understood as recent molecular work has brought some resolution to taxonomy and many historical records may be composed of more than one western Anodonta species. It is believed to occur in California, Oregon, Washington, and across southern British Columbia (north to 52 degrees N latitude) except Vancouver Island, possibly east to Utah (where it may be extirpated) with Idaho records believed to be A. kennerlyi. British Columbia records for A. californiensis are now believed to be applicable to this species. A proper conservation assessment requires further taxonomic study clarifying the placement of western Anodonta species, all of which are largely in decline with local extirpations and range-wide reductions.
Range Extent Comments
This Range Extent analysis only includes occurrences of the putative A. nuttalliana species concept by Chong et al. (2008) and excludes those of A. californiensis, a closely related species in the same clade (Mock et al. 2010, Chong et al. 2008). Reported occurrences are not always in agreement: Blevins et al. (2017) included British Columbia, Canada; Arizona, California, Idaho, Nevada, Oregon, Utah, Washington, Wyoming, USA; Chihuahua, Sonora, Mexico that provided a Range Extent of 2,086,110 square km. Mock (2010) and Nedeau et al. (2005) included California, Oregon, Washington, southern British Columbia; east to Utah (Burch 1975); Idaho records (Henderson, 1924; 1936) records believed to be Anodonta kennerlyi. Wyoming records were identified as A. californiensis and proposals to find extant and additional populations in the Bear River drainage using eDNA and visual surveys are expected to occur for the next couple years (L. Tronstad pers. comm. 2018). Preliminary analysis (K. Mock, Utah State University, pers. comm.) indicates Utah Anodonta are distinct from A. oregonensis of the Pacific northwest and should tentatively be assigned to A. californiensis pending future taxonomic work. Clarke (1981) cites distribution as the Fraser and Columbia River systems in southern British Columbia (absent from Vancouver Island) and south to central California.
There are reports of A. nuttalliana from Mexico; however, all of the records from Mexico available on MUSSELp Database (Graf and Kummings 2018), are presently identified as other Anodonta species (mostly A. impura) on database websites of the respective institutions where they are deposited (Field Museum of Natural History, Museum of Comparative Zoology, US National Museum, Delaware Museum of Natural History,The Academy of Natural Sciences Pennsylvania). Additionally, no other occurrences available from these institutional database websites listed Mexico as a locality for specimens identified as A. nuttalliana. This will likely remain uncertain until taxonomy has better resolution and sufficient field surveys accurately document western Anodonta species.
Occurrences Comments
Number of Occurrences for this Anodonta nuttalliana review did not include records of A. californiensis, a closely related species in the same clade (Mock et al. 2010, Chong et al. 2008). Historical records with uncertain identifications, sympatry, and morphological inconsistencies between species further confound characterization of its true distribution. Currently it is believed to occur in California, Oregon, Washington, southern British Columbia, Arizona, Utah, and Nevada (Mock et al. 2004, 2010, Nedeau et al. 2005, Burch 1975) with some Idaho records (Henderson 1924; 1936) records believed to be Anodonta kennerlyi.
There are reports of A. nuttalliana from Mexico; however, all of the records from Mexico available on MUSSELp Database (Graf and Kummings 2018), are presently identified as other Anodonta species (mostly A. impura) on the respective institutional database websites where they are deposited (Field Museum of Natural History, Museum of Comparative Zoology, US National Museum, Delaware Museum of Natural History,The Academy of Natural Sciences Pennsylvania). Additionally, no other occurrences available from these institutional database websites listed Mexico as locality for specimens identified as A. nuttalliana.
Preliminary analysis (K. Mock, Utah State University, pers. comm.) indicates Utah Anodonta should tentatively be assigned to Anodonta californiensis. Clarke (1981) cites distribution as the Fraser and Columbia River systems in southern British Columbia (absent from Vancouver Island) and south to central California. In Canada, it is somewhat common in British Columbia but little concise locality information is available (Metcalfe-Smith and Cudmore-Vokey 2004), however it is now believed records of what was formerly attributed to Anodonta californiensis in British Columbia is now considered Anodonta nuttalliana (BC CDC, pers. comm. 2009). In Oregon, several populations of Anodonta were recently confirmed in the Middle Fork John Day River and the lower main stem of the Umatilla River, but due to the taxonomic confusion surrounding the western Anodonta, identification to species level was not attempted (Brim Box et al. 2003; 2006), although preliminary evidence indicates the John Day River population includes A. californiensis/nuttalliana clade and the Umatilla River population include both A. oregonensis/kennerlyi and A. californiensis/nuttalliana clades in sympatry (K. Mock, Utah State University, pers. comm. 2007). Specimens have also been confirmed in the Upper Quinn and Middle Owyhee drainages in Nevada/Oregon (K. Mock, Utah State University, pers. comm. 2007). Museum specimens (UMMZ) exist for California (San Juaquin River in San Juaquin Co., Coyote Creek in San Jose Co., San Juan Tequesquito Creek in San Benito Co., Clear Lake in Lake Co., Sacramento River in Sacramento Co., North Fork Pit River in Modoc Co.), Utah (Salt Lake City canal, Warm Spring Lake, and Jordan River in Salt Lake Co., Utah Lake in Utah Co., Willow Springs in Tooele Co., Sevier River in Millard Co.), Oregon (Klamath Lake in Klamath Co.), Nevada (Humboldt River in Elko Co., Pyramid Lake in Washoe Co.), and British Columbia (Sumas and Harrison Lakes).
Threat Impact Comments
Threats were documented in literature.
Ecology & Habitat

Habitat

This species occurs in rivers and lakes on muddy and sandy bottoms (Clarke, 1981), especially low gradient, low elevation areas of coastal watersheds (Nedeau et al., 2005).

Reproduction

Little is known about life history and the glochidial host is unknown. They are probably long-term brooders as gravid females have been observed in October (Nedeau et al., 2005).
Other Nations (2)
United StatesN3
ProvinceRankNative
NevadaSNRYes
OregonS2Yes
CaliforniaSNRYes
UtahS2Yes
WashingtonS1Yes
WyomingSNRYes
CanadaN4
ProvinceRankNative
British ColumbiaS4Yes
Threat Assessments
ThreatScopeSeverityTiming
2 - Agriculture & aquacultureRestricted (11-30%)Moderate or 11-30% pop. declineHigh (continuing)
2.3 - Livestock farming & ranchingRestricted (11-30%)Moderate or 11-30% pop. declineHigh (continuing)
3 - Energy production & miningRestricted (11-30%)Moderate or 11-30% pop. declineHigh (continuing)
3.2 - Mining & quarryingRestricted (11-30%)Moderate or 11-30% pop. declineHigh (continuing)
7 - Natural system modificationsRestricted (11-30%)Moderate or 11-30% pop. declineHigh (continuing)
7.2 - Dams & water management/useRestricted (11-30%)Moderate or 11-30% pop. declineHigh (continuing)
7.2.1 - Abstraction of surface water (domestic use)Restricted (11-30%)Moderate or 11-30% pop. declineHigh (continuing)
7.2.3 - Abstraction of surface water (agricultural use)Restricted (11-30%)Moderate or 11-30% pop. declineHigh (continuing)
8 - Invasive & other problematic species, genes & diseasesRestricted (11-30%)Moderate or 11-30% pop. declineHigh (continuing)
8.1 - Invasive non-native/alien species/diseasesRestricted (11-30%)Moderate or 11-30% pop. declineHigh (continuing)
8.2 - Problematic native species/diseasesRestricted (11-30%)Slight or 1-10% pop. declineHigh (continuing)
9 - PollutionRestricted (11-30%)Slight or 1-10% pop. declineHigh (continuing)
9.1 - Domestic & urban waste waterRestricted (11-30%)Slight or 1-10% pop. declineHigh (continuing)
9.3 - Agricultural & forestry effluentsSmall (1-10%)Moderate or 11-30% pop. declineHigh (continuing)
9.3.3 - Herbicides and pesticidesSmall (1-10%)Moderate or 11-30% pop. declineHigh (continuing)

Roadless Areas (5)
Utah (5)
AreaForestAcres
Fishlake MountainFishlake National Forest25,217
Hilgard MountainFishlake National Forest28,389
Little CreekFishlake National Forest11,479
Mt. ArvineFishlake National Forest6,054
TibadoreFishlake National Forest9,266
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