“…Meerow (2010) characterized the Andean tetraploid clade’s polyploid genome as grist for the mill of the Andean orogeny. Northern Peru in particular, comprising in part the Neotropical bioprovinces Cauca, Desert and Ecuadorian ( Morrone, 2014 ), with its complex of microhabitats, has been a hotspot of diversification in the Andean clade ( Meerow and van der Werff, 2004 ; Meerow and Cano, 2019 ; Meerow and Nakamura, 2019 ; Esquerre and Meerow, 2020 ). The distributions of Rauhia in Peru and Phaedranassa in Ecuador ( Meerow, 1990 ; Oleas et al, 2012 , 2013 , 2016 ) fit the allopatric models of dispersal or vicariance ( Figure 10 and Supplementary Figure 9 ) followed by isolation described for Andean complexes of Buddleja L. ( Norman, 2000 ), Calceolaria L. ( Molau, 1988 ), Fuchsia L. ( Berry, 1982 ), and many other taxa ( Ayers, 1999 ; Beck and Richter, 2008 ; Antonelli et al, 2009 ; Pennington et al, 2010 ; Anthelme et al, 2014 ; Luebert and Weigend, 2014 ; Bacon et al, 2018 ).…”