Bivalvia | Unionida | Unionoidea | Unionidae | Unioninae | Anodontini | Alasmidontina

genus Strophitus Rafinesque, 1820: cladomics

5 Recent valid species (8 total species)

Cladomics pages are experimental — even more so than the rest of this site!

The purpose of the cladomics pages for each genus and family-group level taxon is to provide statistics and references indicating the extent to which published phylogenetic work supports the classification used here.

The Cladomics Summary provides an overview of the number of studies that have included terminal species representing this taxon as well as an indication of how frequently it has been recovered as monophyletic.

Following the summary, the available published clades representing the taxon are listed.

For more information, visit the Cladomics FARQ (frequently asked rhetorical questions) page. Abbreviations for the various statistics are explained on the FARQ!

Cladomics Summary

number of species = 5 (8 total)
analyzed in 54 cladograms in 37 publications
maximum number of terminals in an analysis = 5 (mean = 1.48, median = 1)

Basic Monophyly

number of cladograms that test basic monophyly (i.e., more than 1 included species) = 8
maximum number of included terminals = 5, (mean = 4.25 median = 4.5)
proportion of cladograms that support basic monophyly = 1

Pairwise Cladogram Clustering

The graphs below depict in two dimensions all pair-wise ingroup distances within the cladome. See the Cladmoics FARQ for more information.

Cladograms

Perkins et al., 2025 [Publ 4447], fig. 2_mtDNA-ITS

** Top Monophyly Cladogram ** ** Top Sister-Group Cladogram **

Campbell & Lydeard, 2026 [Publ 4810], fig. 6-14

Smith et al., 2018 [Publ 3790], fig. 1

Smith et al., 2023 [Publ 4291], fig. 2

Whelan et al., 2023 [Publ 4287], fig. 2

Whelan et al., 2023 [Publ 4287], fig. 3

Whelan et al., 2023 [Publ 4287], fig. 4

Krebs et al., 2003 [Publ 2691], fig. 3

Inoue et al., 2018 [Publ 3858], fig. 1_3a-c

Boyer et al., 2011 [Publ 2718], fig. 4

Inoue et al., 2014 [Publ 3635], fig. 3A

Chong et al., 2008 [Publ 2668], fig. 3

Breton et al., 2011 [Publ 3376], fig. 3

Chase et al., 2018 [Publ 3847], fig. 4

King et al., 1999 [Publ 2699], fig. 2

Boyer et al., 2011 [Publ 2718], fig. 3

Hewitt et al., 2018 [Publ 3758], fig. 5

Huang et al., 2019 [Publ 3843], fig. 2

Huang et al., 2019 [Publ 3843], fig. S3

Huang et al., 2019 [Publ 3843], fig. S4

Stewart et al., 2021 [Publ 4451], fig. 1

Lydeard et al., 1996 [Publ 2656], fig. 3

Lydeard et al., 1996 [Publ 2656], fig. 4

King et al., 1999 [Publ 2699], fig. 4

Huang et al., 2002 [Publ 2657], fig. 1

Huang et al., 2002 [Publ 2657], fig. 2

Lopes-Lima et al., 2017 [Publ 3745], fig. 1-2

Bolotov et al., 2017 [Publ 3761], fig. S1

Bolotov et al., 2017 [Publ 3761], fig. S2

Bolotov et al., 2017 [Publ 3764], fig. S1

Bolotov et al., 2018 [Publ 3826], fig. 2

Lopes-Lima et al., 2020 [Publ 4080], fig. 2-4

Jeratthitikul et al., 2022 [Publ 4260], fig. S1_1

Jeratthitikul et al., 2022 [Publ 4260], fig. S2_2

Graf & Ó Foighil, 2000 [Publ 2648], fig. 2A

Graf & Ó Foighil, 2000 [Publ 2648], fig. 2B

Graf & Cummings, 2006 [Publ 1968], fig. 2

Hoeh et al., 2009 [Publ 2716], fig. 3

Hoeh et al., 2009 [Publ 2716], fig. 4

Hoeh et al., 2009 [Publ 2716], fig. 5

Jadhav & Jamkhedkar, 2009 [Publ 3697], fig. 11

Wu et al., 2018 [Publ 3836], fig. 2

Pfeiffer & Graf, 2013 [Publ 3531], fig. 2

Wu et al., 2021 [Publ 4366], fig. 2_I

Wu et al., 2021 [Publ 4366], fig. 6

Wu et al., 2023 [Publ 4296], fig. 4

Liu et al., 2023 [Publ 4310], fig. 4

Liu et al., 2023 [Publ 4310], fig. 5

Bogan & Hoeh, 2000 [Publ 2650], fig. 1

Hoeh et al., 2001 [Publ 2652], fig. 14f2

Hoeh et al., 2001 [Publ 2652], fig. 14f4

Hoeh et al., 2002 [Publ 2653], fig. 2

Roe & Hoeh, 2003 [Publ 2655], fig. 4f2

Roe & Hoeh, 2003 [Publ 2655], fig. 4f3