Bivalvia | Unionida | Unionoidea | Unionidae | Ambleminae | Amblemini

genus Reginaia Campbell & Lydeard, 2012: cladomics

3 Recent valid species (3 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 = 3 (3 total)
analyzed in 36 cladograms in 22 publications
maximum number of terminals in an analysis = 2 (mean = 1.58, median = 2)

Basic Monophyly

number of cladograms that test basic monophyly (i.e., more than 1 included species) = 21
maximum number of included terminals = 2, (mean = 2 median = 2)
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

Campbell et al., 2005 [Publ 2660], fig. 1

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

Campbell et al., 2005 [Publ 2660], fig. 2

Campbell & Lydeard, 2012 [Publ 3308], fig. 1

Campbell & Lydeard, 2012 [Publ 3308], fig. 2

Campbell & Lydeard, 2012 [Publ 3308], fig. 3

Campbell & Lydeard, 2012 [Publ 3308], fig. 4

Campbell & Lydeard, 2012 [Publ 3309], fig. 1-2

Campbell & Lydeard, 2012 [Publ 3309], fig. 3

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

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

Inoue et al., 2013 [Publ 3528], fig. 3

Pfeiffer et al., 2016 [Publ 3660], fig. 2

Pfeiffer et al., 2019 [Publ 3866], fig. 1

Inoue et al., 2020 [Publ 3941], fig. 3

Inoue et al., 2020 [Publ 3941], fig. 4

Inoue et al., 2020 [Publ 4128], fig. 2

Inoue et al., 2020 [Publ 4128], fig. 3

Lydeard et al., 2000 [Publ 2654], fig. 2a

Lydeard et al., 2000 [Publ 2654], fig. 2b

Lydeard et al., 2000 [Publ 2654], fig. 2c

Lydeard et al., 2000 [Publ 2654], fig. 2d

Serb et al., 2003 [Publ 2659], fig. 2

Serb et al., 2003 [Publ 2659], fig. 3

Pfeiffer et al., 2019 [Publ 3937], fig. 4-5

Pfeiffer et al., 2019 [Publ 3937], fig. 6

Smith et al., 2019 [Publ 3951], fig. 2

Smith et al., 2020 [Publ 4129], fig. 1

Smith et al., 2020 [Publ 4129], fig. 2-3

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

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

Burlakova et al., 2019 [Publ 3899], fig. 1

Barraza et al., 2026 [Publ 4851], fig. 3

Burdick & White, 2007 [Publ 2679], fig. 3

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

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

Hauck et al., 2023 [Publ 4333], fig. 9