Tax. = taxonomic unit of comparison:
Sp = single species occurring in both North America (NA) and South America (SA).
Sp-InC = the same two infraspecies (varieties or subspecies) occurring in both NA and SA.
Sp-InD = two different infraspecies (varieties or subspecies) occurring in both NA and SA.
Sp-Sp = two different species, either sister- or closely related, occurring in NA and SA.
Sp-Cl = a single species in the source region sister to a clade (of two or more species) in the recipient region.
Cl-Sp = a clade (of two or more species) in the source region sister to a single species in the recipient region.
Cl-Cl = a clade sister to another clade. For taxa names, [ ] = synonym(s).
Dist. = distribution:
AAD = American amphitropical disjust distribution generally well outside of tropical regions.
eN = AAD distribution in eastern North America.
eS = AAD distribution in eastern South America.
eNS = AAD distribution in eastern North America and eastern South America.
ewN = AAD distribution in eastern and western North America.
tN = trans-North America, distribution significantly entering North American tropical zone.
tS = trans-South America, distribution significantly entering South American tropical zone.
tNS = trans-North and South America, distribution significantly entering North American and South American tropical zones.
* = native distribution also occurring outside the western hemisphere.
C#-NA = chromosome number of North American taxon.
C#-SA = chromosome number of South American taxon.
(Taxa specific to a count are indicated in parentheses; less commonly obtained chromosome counts or ploidy levels are indicated in brackets.)
Dur./Hab. = plant duration, either A = annual, B = biennial, P = perennial, or a combination, and plant habit, either H = herb, S = shrub, T = tree, or a combination.
Disp. Dir. = direction of dispersal or migration from source area to recipient area as determined from phylogenetic studies, either N->S (NA to SA), S->N (SA to NA), or Equivocal.
Div. mya = mean time (mean ranges in parentheses) of divergence of NA and SA taxa/clades, either stated in or calculated from (*) literature soures.
Lit. Source = Literature source of phylogenetic or pertinent taxonomic studies, including those citing direction or time of divergence.
"—" = missing information. Distribution links largely from the Global Biodiversity Information Facility (GBIF).
** = not considered bipolor by Moore and Chater (1971)..
No. | Region | GROUP | Family | Genus | Tax. | Dist. | AAD Taxon/Clade-NA | SynonymyNA | Dur.-Hab. | NA Distribution: BLZ,CAN,CRI,GTM,HND,MEX,NIC,PAN,SLV,USA | NA Distribution: Data Source | C#-NA | Chrom.Lit.-NAm | AAD Taxon/Clade-SA | SynonymySA | SA Distribution: ARG,BRA,BOL,CHL,COL,ECU,PER,PRY,URY,VEN | SA Distribution: Data Source | C#-SA | Chrom.Lit.-SAm | Div. mya-Late | Div. mya-Early | Div. mya-Mean | Notes | Disp. Dir. | Lit. Source |
1 | Bipoloar | FERN | Ophioglossaceae | Botrychium | Sp-Sp | AAD | Botrychium spathulatum W.H.Wagner | Botrychium lunaria (L.) Sw. _ Botrychium campestre W.H.Wagner & Farrar | P-H | CAN,USA | GBIF, 2017; USDS-NRCR, 2017 | B. l.: 2n = 90 [2x] | Dauphin, et al., 2016 | Botrychium dusenii (Christ) Alston | Botrychium lunaria (L.) Sw. var. dusenii Christ | ARG,CHL | Zuloaga et al., 2008 | [4x] | Farrar and Stensvold, 2017 | 0.3 | Farrar and Stensvold, 2017 | ||||
2 | Bipoloar | Pteridaceae | Cryptogramma | Sp-Sp | AAD | Cryptogramma acrostichoides R.Br. | Cryptogramma crispa (L.) R.Br. ex Hook. var. acrostichoides (R.Br.) C.B.Clarke | P-H | CAN,USA | GBIF, 2017; USDS-NRCR, 2017 | — | Cryptogramma fumariifolia Christ | Cryptogramma crispa var. chilensis (Christ) Looser | ARG,CHL | Zuloaga et al., 2008 | — | |||||||||
3 | Bipoloar | MONOCOT | Cyperaceae | Carex | Sp | AAD* | Carex arctogena L. | P-H | CAN,USA[Europe] | GBIF, 2017; USDS-NRCR, 2017 | — | " | ARG,CHL | Zuloaga et al., 2008 | — | 0 | N->S | Villaverde et al., 2015a | |||||||
4 | Bipoloar | Sp | AAD* | Carex canescens L., s.l. | P-H | CAN,USA[Asia, Europe, Australia] | GBIF, 2017; USDS-NRCR, 2017 | 2n = 54, 56 | Roalson, 2008 | " | ARG,CHL | Zuloaga et al., 2008 | — | 0 | 0.17 | 0.05 | N->S | Villaverde et al., 2017 | |||||||
5 | Bipoloar | Sp | AAD | Carex macloviana D’Urv. | P-H | CAN,USA | GBIF, 2017; USDS-NRCR, 2017 | 2n = 86 | Roalson, 2008 | " | ARG,CHL | Zuloaga et al., 2008 | — | 0.09 | 0.48 | 0.27 | SA pops possibly diphyletic; see Márquez-Corro et al., 2017 | Equiv | Escudero et al., 2010; Márquez-Corro et al., 2017 | ||||||
6 | Bipoloar | Sp-InD | AAD | Carex magellanica Lam. subsp. irrigua (Wahlenb.) Hiitonen | P-H | CAN,USA | GBIF, 2017; USDS-NRCR, 2017 | 2n = ca. 60 | Roalson, 2008 | Carex magellanica Lam. subsp. m. | ARG,CHL | Zuloaga et al., 2008 | — | 0 | 0.39 | 0.2 | N->S | Escudero et al., 2010 | |||||||
7 | Bipoloar | Sp | AAD* | Carex maritima Gunnerus, s.l. | Carex incurva Lightf. | P-H | CAN,USA[Europe] | GBIF, 2017; USDS-NRCR, 2017 | 2n = 60 | Roalson, 2008 | " | ARG,CHL | Zuloaga et al., 2008 | — | 0.03 | 0.51 | 0.23 | 3 changes in ITS (607 bp long), 1 bp change in rps-16 Chile-NA/Europe | N->S | Villaverde et al., 2015b | |||||
8 | Bipoloar | Sp | AAD* | Carex microglochin Wahlenb. | P-H | CAN,USA[Asia,Europe] | GBIF, 2017; USDS-NRCR, 2017 | — | " | ARG,CHL | Zuloaga et al., 2008 | — | 12 changes in ITS, but not sister taxa | Escudero et al., 2010 | |||||||||||
9 | Bipoloar | Eleocharis | Sp | AAD* | Eleocharis quinqueflora (Hartmann) O.Schwarz s.l.** | Eleocharis pauciflora (Lightf.) Link, Eleocharis atacamensis Phil. | P-H | CAN,USA[Asia,Europe] | GBIF, 2017; USDS-NRCR, 2017 | 2n = ca. 136 | Raven, 1963 | " | ARG,CHL | Zuloaga et al., 2008 | — | What we are treating as Eleocharis quinqueflora s.l. may be a complex of species; see Guaglianone et al., 2009 | |||||||||
10 | Bipoloar | Juncaginaceae | Triglochin | Sp | AAD* | Triglochin palustris L. | P-H | CAN,USA[Asia,Europe] | GBIF, 2017; USDS-NRCR, 2017 | 2n = 24 | Raven, 1963 | " | ARG,CHL | Zuloaga et al., 2008 | — | ||||||||||
11 | Bipoloar | Poaceae | Alopecurus | Sp | AAD* | Alopecurus magellanicus Lam. | Alopecurus alpinus J.E.Sm., Alopecurus antarcticus Vahl | P-H | CAN,USA[Asia,Europe] | GBIF, 2017; USDS-NRCR, 2017 | — | " | ARG,CHL | Zuloaga et al., 2008 | — | ||||||||||
12 | Bipoloar | Avenella | Sp | AAD* | Avenella flexuosa (L.) Drejer | Deschampsia flexuosa (L.) Trin. | P-H | CAN,USA[Europe] | GBIF, 2017; USDS-NRCR, 2017 | — | " | ARG,CHL | Zuloaga et al., 2008 | — | |||||||||||
13 | Bipoloar | Calamagrostis | Sp | AAD* | Calamagrostis stricta (Timm.) Koel. | Calamagrostis neglecta (Ehrh.) P.Gaertn., B.Mey. & Schreb. | P-H | CAN,USA[Europe] | GBIF, 2017; USDS-NRCR, 2017 | — | " | Deyeuxia poaeoides (Steud.) Rúgolo | ARG,CHL | Flora del Cono Sur, 2017 | — | ||||||||||
14 | Bipoloar | Catabrosa | Sp | AAD* | Catabrosa aquatica (L.) Beauv. | P-H | CAN,USA[Europe] | GBIF, 2017; USDS-NRCR, 2017 | 2n = 20 | Raven, 1963 | " | ARG,CHL | Flora del Cono Sur, 2017 | — | Flora del Cono Sur, 2017, indicates that Catabrosa aquatica is non-native ("Adventicia") in the Cono Sur. But considered native by the World Checklist of Selected Plant Families, and by Robert J. Soreng (personal communication). | ||||||||||
15 | Bipoloar | Deschampsia | Sp | AAD* | Deschampsia caespitosa (L.) P.Beauv. | P-H | CAN,USA[Europe] | GBIF, 2017; USDS-NRCR, 2017 | 2n = 26, 28 | Raven, 1963 | " | Deschampsia caespitosa (L.) P. Beauv. var. caespitosa, var. pulchra (Nees & Meyen) Nicora | ARG,BRA,CHL | Zuloaga et al., 2008 | — | ||||||||||
16 | Bipoloar | Phleum | Sp | AAD* | Phleum alpinum L. | P-H | CAN,USA[Europe] | GBIF, 2017; USDS-NRCR, 2017 | 2n = 28 | Dalgaard, 1988 | " | ARG,CHL | Zuloaga et al., 2008 | 2n = 28 | Moore, 1981 | ||||||||||
17 | Bipoloar | Vahlodea | Sp | AAD* | Vahlodea atropurpurea (Wahlenb.) Fr. | Deschampsia atropurpurea (Wahlenb.) Scheele | P-H | CAN,USA[Europe] | GBIF, 2017; USDS-NRCR, 2017 | 2n = 14 | Raven, 1963 | " | ARG,CHL | Flora del Cono Sur, 2017 | — | ||||||||||
18 | Bipoloar | EUDICOT | Brassicaceae | Cardamine | Sp-Sp | AAD* | Cardamine pratensis L. | P-H | CAN,USA[Europe] | GBIF, 2017; USDS-NRCR, 2017 | — | Cardamine glacialis (G.Forst.) DC. | ARG,CHL | Flora del Cono Sur, 2017 | — | ||||||||||
19 | Bipoloar | Draba | Sp-Sp | AAD* | Draba incana L. | BP-H | CAN,USA[Europe] | GBIF, 2017; USDS-NRCR, 2017 | — | Draba magellanica Lam. | ARG,CHL | Flora del Cono Sur, 2017 | — | ||||||||||||
20 | Bipoloar | Ericaceae | Empetrum | Sp-Sp | AAD* | Empetrum nigrum L. | P-S | CAN,USA[Europe] | GBIF, 2017; USDS-NRCR, 2017 | — | Empetrum rubrum Vahl ex Willd. | ARG,CHL | Flora del Cono Sur, 2017 | — | 0.56 | 0.93 | 0.69 | N->S | Popp et al., 2011 | ||||||
21 | Bipoloar | Gentianceae | Gentiana | Sp | AAD* | Gentiana prostrata Haenke | ABP-H | CAN,USA[Europe] | GBIF, 2017; USDS-NRCR, 2017 | — | " | ARG,CHL | Flora del Cono Sur, 2017 | — | |||||||||||
22 | Bipoloar | Plantaginaceae | Hippuris | Sp | AAD* | Hippuris vulgaris L. | P-H | CAN,MEX,USA[Europe] | Villaseñor, 2016; GBIF, 2017; USDS-NRCR, 2017 | — | " | ARG,CHL | Flora del Cono Sur, 2017 | — | |||||||||||
23 | Bipoloar | Plantago | Sp | AAD* | Plantago maritima L. | Plantago maritima L. subsp. juncoides (Lam.) Hulten | P-H | CAN,USA[Europe] | GBIF, 2017; USDS-NRCR, 2017 | — | " | Halerpestes cymbalaria (Pursh) Greene | ARG,CHL | Flora del Cono Sur, 2017 | — | Plantago maritima var. scabrior (Pilg.) Pilg. also occurs in s. Patagonia | |||||||||
24 | Bipoloar | Plumbaginaceae | Armeria | Sp | AAD* | Armeria maritima (Mill.) Willd. | Armeria maritima (Mill.) Willd. subsp. californica (Boiss.) A.E.Porsild | P-H | CAN,USA[Europe] | GBIF, 2017; USDS-NRCR, 2017 | 2n = 18 | Raven, 1963 | " | ARG,CHL | Flora del Cono Sur, 2017 | — | A second, possibly independent disjunction is suggested by a related form with more conspicuous but still monomorphic flowers which occurs along the Pacific Coast of NA from s. Brit. Col. to central Calif. (also n =9) and again in s. Chile (H. G. Baker. 1954. Rapp. Comm. Intern. Congr. Botan., Paris, sect. 10, pp. 190-191; Am. Naturalist, 93: 255-272, 1959; and pers. commun.) | ||||||||
25 | Bipolar | Polygonaceae | Koenigia | Sp | AAD* | Koenigia islandica L. | A-H | CAN,USA[Europe] | GBIF, 2017; USDS-NRCR, 2017 | 2n = 28 | Raven, 1963 | " | ARG,CHL | Flora del Cono Sur, 2017 | — | ||||||||||
26 | Bipoloar | Ranunculaceae | Anemone | Sp | AAD | Anemone multifida Poir.** | P-H | CAN,USA | USDA-NRCS, 2017 | 2n = 32 [4x] | Löve, 1982a | " | ARG,CHL | Zuloaga et al., 2008 | 2n = 16, 32 [4x], 64 [6x] | Moore, 1981; Ziman et al., 2006 | Of hybrid origin from taxa in NA (Meyer et al., 2010): "Our results (fig. 1) indicate that A. multifida may be a cross between a member of the montane/alpine clade consisting of A. drummondii, A. parviflora, and A. lithophila and a member of the more temperate clade consisting of A. sylvestris, A. virginiania, A. riparia, and A. cylindrica, all North American species. If true, this helps to explain the diverse habitats (from sand dunes to montane and alpine environments) and geographical range (discontinuous range in North America and South America) occupied by A. multifida. | N->S | Meyer et al., 2010; Hoot et al., 2012 | ||||||
27 | Bipoloar | Ranunculus | Sp-Sp | AAD* | Ranunculus hyperboreus Rottb.** | P-H | CAN,USA[Europe] | GBIF, 2017; USDS-NRCR, 2017 | 2n = 32 | Krogulevich, 1976; Engelskjon, 1979; Zhukova, 1980; Zhukova, 1982; Malakha, 1990 | Ranunculus fuegianus Speg.** | ARG,CHL | Zuloaga et al., 2008 | 2n = 48 | Moore, 1981 | Ranunculus bonariensis Poir. var. trisepalus (Gill.) Lourteig | N->S? | Paun et al., 2005 |