June 14, 2023

BRAZILIAN NATIVE BRASSICACEAE

PUBLISHED IN 02.02.2023 

Brassicaceae is a remarkable family composed mainly of herbs from temperate (rarely in tropical mountainous regions), being quite diverse in the region of East Asia, the Mediterranean basin, Central Asia and North America. Plants of the World On Line (POWO) recognizes 345 genera in Brassicaceae (SEE), while BrassiBase, a platform dedicated exclusively to the family, points to 351 genera, with 3,977 spp. within 52 tribes (SEE). The family is marked by an exorbitant amount of naturalized, cultivated and invasive species in various parts of the world, so the vast majority of local treatments of the group contain many citations of non-native species and genera, at various scales.

In terms of native diversity, in addition to the regions of the northern hemisphere already mentioned, it is worth mentioning interesting radiations from the Andean and Patagonian region of South America, South Africa and Australia, all with many endemic genera. Few genera occur in tropical zones, most restricted to mountainous regions. In Africa, for example, few genera colonized the African highlands, to mention prominently Arabis, Arabidopsis, Crambe, Diceratella, Oreophyton, Sisymbrium, Subularia, Mummenhoffia and Turritis; tribe Microlepidieae (16/55) has a extraordinary radiation in Australia region; in southern Africa, three near restricted genera occur: Aplanodes, Chamira and Heliophila, the latter with c. 100 spp., very distinct morphologically.

Morphologically, Brassicaceae are mostly delicate herbs, but there are a lot of sessile rosettes, dendroid rosettes and succulents, aquatic herbs, large shrubs, small arctic tundra herbs, thorny shrubs from North Africa, some rare lianas, nanoplants from snow line and high mountains, but saplings (or larger), woody lianas and epiphytes are virtually absent. The Brassicaceae are easily distinguished by the cruciform corolla and tetradynamous stamens. The exceptions are in some species of Lepidium that have only two stamens and a rudimentary or absent corolla.

In New World there are c. 1,170 spp., c. 400 in South America; the only native Neotropical crop is Lepidium meyenii (maca) cultivated in the high Peruvian Andes and consumed locally.

There is almost no academic work focused on the family in Brazil, which is surprising given that the family represents one of the most interesting and explored in the botanical literature of many neighboring countries. With the objective of creating a point of support in this discussion, NSAA made a review of Brassicaceae in Brazil, using as reference the species cited as Brazilian in POWO (SEE), each one being analyzed within the scope of the VPA and the records of each one. in Species Link (SEE), with eventual complement from other sources, such as Zuloaga et al. (Darwiniana, 2019). Maps were edited based on these records, one per genus, and some referenced images were added. In some genera, we excluded some records due to the fact that they are too disjoint from the occurrence bulk of a given species, suggesting that they are material incorrectly identified, or non-native material.

In this analysis we identify 4 genera and 11 spp. native in Brazil, two endemics, both known only the type collection.

TAXONOMY

Brassicaceae includes two subfamilies, Aethionemoideae (1/58) and Brassicoidae (remaining), the latter with five subtribes, Arabodae (117/c. 1,190, Arabideae, Alysseae, Asperuginoideae, Stevenieae), at South America with 84 spp. in two genera from Venezuela to Argentina and Chile; Heliophilodae (22/c. 111, Anastaticeae, Asteae, Biscutelleae, Chamireae, Cremolobeae, Eudemeae, Heliophileae, Hillielleae, Iberideae, Megacarpaeeae Notothlaspideae, Schizopetaleae, Subularieae) from S and E Europe, Mediterranean, W Asia, Mexico, Himalayas, Siberia, Russian Far East, Alaska, Yukon and South America; and Hesperodae (Eurasia, Anchonieae, Buniadeae, Chorisporeae, Dontostemoneae, Euclidieae, Hesperideae, Shehbazieae) does not occur in Brazil.

Andrzeiowskia (1, SE Europe, SW Asia), Raphanorhyncha (1, Mexico), Veselskya (1, Afghanistan) are unplaced Brassicaceae.

ADAPTED PHYLOGENY OF BRASSICACEAE WITH EMPHASIS ON CLADES WITH NATIVE BRAZILIAN SPECIES

1. SUPERTRIBE CAMELINODAE

16 lineages, Alyssopsideae, Arabidopsideae, Boechereae, Beilstein, Camelineae, Cardamineae, Crucihimalayeae, Descurainieae, Erysimeae, Halimolobeae, Hemilophieae, Lepidieae, Malcolmieae, Microlepidieae, Oreophytoneae, Physarieae, Smelowskieae, Turritideae, Yinshanieae, 11 of them absent in South America. For South Americans, tribes Descuiraneae (6/c. 45, 12 spp. in three genera from Venezuela to Argentina and Chile), Physarieae (7/133, only six sp. of Physaria (Nutt. ex. Torr. & A. Gray) A. Gray. from Bolivia, Argentina and Uruguay) and Halimolobeae (6/39, 13 spp. in 4 genera from Venezuela to Argentina and Chile) does not occur in Brazil. Brazilian members belogs tribes Cardamineae and Lepidieae.

1.1 Tribe Cardamineae - c. 12 genera and c. 335 spp., almost all from northern hemisphere south up to Mexico except Aplanodes (2) in South Africa and Lesotho, and two subcosmopolitan, Rorippa and Cardamine.

Cardamine L.

Annuals, biennials, or perennials, usually rhizomatous, sometimes tuberiform, stoloniferous or caudex; not scapose, often subscapose; glabrous or pubescent. Stems erect, ascending, decumbent, or prostrate, unbranched or branched. Leaves: cauline, rhizomal, or basal; rhizomal and basal rosulate or not, petiolate, blade margins entire, toothed, or 1-3-pinnatisect, or palmately lobed, sometimes trifoliolate, pinnately, palmately, or bipinnately compound (leaflets petiolulate, subsessile, or sessile); cauline (usually alternate, rarely opposite or whorled) petiolate or sessile, blade (base cuneate, attenuate, or auriculate to sagittate), margins entire, dentate, or variously lobed, (leaflets petiolulate or sessile). Racemes (corymbose or paniculate, bracteate in C. pattersonii), elongated in fruit. Fruiting pedicels erect, ascending, divaricate, or reflexed, slender or stout. Flowers: sepals (caducous), usually erect, rarely spreading or ascending, ovate or oblong, lateral pair saccate or not basally, (usually glabrous, rarely pubescent); petals (rarely absent), white, pink, purple, or lilac, obovate, spatulate, or oblanceolate, claw absent or strongly differentiated from blade, (apex obtuse, rounded, emarginate, or subemarginate); stamens (6, rarely 4), equal in length; filaments not dilated basally; anthers ovate, oblong, or linear, (apex obtuse), glabrous [rarely pubescent]; nectar glands confluent, lateral glands annular or semiannular, subtending bases of stamens, median glands present (2, rarely 4) or absent. Fruits siliques, sessile, usually linear, rarely narrowly oblong or narrowly lanceolate, smooth or torulose, latiseptate; valves (papery, elastically dehiscent, becoming spirally or circinately coiled) each not veined, glabrous or, rarely, pubescent; replum strongly flattened; septum complete, (membranous); ovules 4-80 per ovary; style usually distinct, rarely obsolete; stigma capitate. Seeds uniseriate, flattened, usually not winged, rarely margined or winged, oblong, ovoid, or globose; seed coat (smooth, minutely reticulate, colliculate, or rugose) mucilaginous or not when wetted; cotyledons accumbent, rarely incumbent. x = 7, 8 (FNA).

DISTRIBUITON 260 spp., mainly restricteds for a single landmass region: C & E Asia from E Siberia to Philipppines (c. 65 spp.), northern Eurasia from Azores to Turkey and Siberia (c. 50 spp.), Arctic Canada to Central America and Caribbean (c. 40 spp., C. ocoana O.E.Schulz endemic to Dominican Republic), Australia to New Zealand and adjacent islands (c. 55 spp.), South America (27 exclusive spp.); tropical Africa and Middle East has only one exclusive species each; Australasia from Indonesia to New Caledonia has only three exclusive species (New Guinea and Java with endemics).

14 non South American spp. extrapolate this pattern, being seven spp. from Eurasia up to North America; C. trichocarpa Hochst. ex A.Rich. from tropical Africa to India; C. macrophylla Willd. and C. impatiens L. from Europe to tropical China and India; C. hirsuta L. and C. flexuosa With. from Europe and tropical Africa to Middle East or New Guinea; C. pratensis L. and C. bellidifolia L. in northern Hemisphere up to U.S.A., Ethiopia and Tibet.

South American has 33 spp., 27 exclusives, C. obliqua Hochst. ex A.Rich. and C. africana L. are amphitropical, native from tropical Africa and from Mexico to Ecuador, the latter also in southern Asia, Australasia and S & SE South America inc. Brazil; C. ovata Benth., C. jamesonii Hook., C. bonariensis Pers. and C. fulcrata Greene occur from Central America, Caribbean or Mexico to South America. For 27 South American exclusives, VPA reconizes only 19. Endemic species in South America occur in Bolivia (2), Chile (6), Colombia (1), Ecuador (3), Uruguay (1, C. subterranea Larrañaga) and Venezuela (1).

IN BRAZIL Salariato & Zuloaga (Darwiniana, 2020) cites C. bonariensis Pers. and C. chenopodiifolia Pers. in Brazil; POWO lists these same two plus C. africana L. (SEE); VPA and Reflora cites only C. chenopodifolia (SEE Reflora). This paper recognizes the three from POWO; for several phylogeny from Cardamine, se works of Carlsen et al. (Annals of the Missouri Botanical Garden, 2009), W. Bleeker et al. (Australian Systematic Botany, 2002) and Marhold (American Journal of Botany, 2006).

1. Cardamine africana L. ‣ subpantropical species, from tropical & S Africa, Yemen, India to W Malesia, Guatemala to Ecuador, Bolivia, Argentina and S & SE Brazil. In Brazil occur in small places in Minas Gerais, Rio de Janeiro, São Paulo, Paraná, Santa Catarina and Rio Grande do Sul states.


2. Cardamine bonariensis Pers. ‣ widely distributed from Mexico to Argentina and S, SE & NE Brazil; widely in Brazil from Paraíba to Rio Grande do Sul state, with a gap between Bahia and Minas Gerais.


3. Cardamine chenopodiifolia Pers. ‣ collected from Bolivia, Argentina, Paraguay and E & SE Brazil. In Brazil is widely from Minas Gerais to Rio Grande do Sul state, with a disjunct record near Bahia state.


Lorem ipsum dolor sit amet, consectetur adipiscing elit, sed do eiusmod tempor incididunt ut labore et dolore magna aliqua. Ut enim ad minim veniam, quis nostrud exercitation ullamco laboris nisi ut aliquip ex ea commodo consequat. Duis aute irure dolor in reprehenderit in voluptate velit esse cillum dolore eu fugiat nulla pariatur. Excepteur sint occaecat cupidatat non proident, sunt in culpa qui officia deserunt mollit anim id est laborum.
 
Cardamine bonariensis Pers. in Santa Catarina state, Brazil © Species Link/Fototeca Paulo Schwirkowski – FPS
Cardamine chenopodiifolia Pers. in Uruguay © floranativadeuruguay.blogspot.com.br
2. Rorippa Scop.

Annuals, biennials, or perennials; (usually aquatic or of mesic habitats, rhizomatous, sometimes with caudex); not scapose; glabrous or pubescent. Stems erect or prostrate, unbranched or branched. Leaves basal and/or cauline; petiolate or sessile; basal (usually withered early), rosulate or not, petiolate, blade margins entire, dentate, sinuate, lyrate, pectinate, or 1-3-pinnatisect; cauline petiolate or sessile, blade (base cuneate, attenuate, auriculate, or sagittate), margins entire, dentate, pinnatifid, or pinnatisect. Racemes slightly to considerably elongated in fruit. Fruiting pedicels erect, suberect, ascending, horizontal, reflexed, or divaricate, usually slender. Flowers: sepals (rarely persistent), erect or spreading, ovate or oblong, lateral pair not or, rarely, saccate basally, (margins often membranous); petals (rarely vestigial or absent), often yellow, sometimes white or pink, usually obovate, spatulate, oblong, or oblanceolate, rarely linear, claw undifferentiated or not from blade, (often shorter than sepals, apex obtuse or emarginate); stamens usually tetradynamous, rarely 4 and equal; anthers usually ovate or oblong, rarely linear, (apex usually obtuse, rarely apiculate); nectar glands confluent, often subtending bases of stamens, median present. Fruits siliques or silicles, usually sessile, rarely shortly stipitate, linear, oblong, ovoid, ellipsoid, pyriform, subglobose, or globose, smooth or torulose, terete or slightly latiseptate; valves papery or leathery, each obscurely veined, glabrous or pubescent; replum (visible), rounded; septum usually complete, rarely perforate; ovules [10-]18-242[-300] per ovary; style obsolete or distinct; stigma capitate, (rarely slightly 2-lobed). Seeds usually biseriate, rarely uniseriate, plump, not or, rarely, winged, oblong, ovoid, ovate, orbicular, cordiform, subglobose, or globose; seed coat (reticulate, colliculate, rugose, tuberculate, or foveolate), mucilaginous or not when wetted; cotyledons accumbent (FNA). 
 
DISTRIBUTION 85 spp., mainly exclusives from a single regiions: Europe inc. Caucasus (13), tropical Africa (3), Pacific islands from Indonesia to Solomon Is. (5, inc. endemics in New Guinea, Java and New Caledonia), Arctic Canada to Costa Rica and Caribbean (20), Australia (4), New Zealand (1), Iran (1), Madagascar and region (2), Marocco (3), S, E & SE Asia (7). Mixed pattern includes Eurasia to Canadá, Australia to New Zealand, Africa to India, Africa to Madagascar, India to Timor one spp. each. 5 spp. are widely distributed in Eurasia; R. indica (L.) Hiern. occur in almost all parts of Old World; R. palustris (L.) Besser occur in over all nothern Hemisphere up to Nicaragua, Sudan and New Guinea.

All 13 South American members by POWO (SEE) are exclusive from continent except Rorippa pinnata (Sessé & Moc.) Rollins, disjuntc from Colombia and Mexico: R. austroamericana Mart.-Laborde (Argentina, Bolivia), R. beckii Al-Shehbaz (Peru, Bolivia), R.bonariensis (Poir.) Macloskie (Ecuador, Peru, Argentina, Paraguay, Brazil), R. clandestina (Spreng.) J.F. Macbr. (Ecuador to Argentina and Brazil), R. coxii (Phil.) L.E. Navas (Chile), R. chubutica (O.E.Schulz) Mart.-Laborde (Argentina and Chile), R. eggersii (O.E. Schulz) J.F. Macbr. (Colombia and Ecuador), R. hilariana (Walp.) Cabrera (Bolivia, Argentina, Paraguay, Brazil), R. mandonii (E. Fourn.) Mart.-Laborde (Colombia to Bolivia and Argentina), R. nana (Schltdl.) J.F. Macbr. (Colombia to Bolivia, S Brazil), R. philippiana (Speg.) Macloskie (Chile) and R. ventanensis Boelcke (Argentina).

VPA recognizes 4 spp. absents in POWO for South America (SEE): R. sarmentosa (Sol. ex G. Forst.) J.F. Macbr., R. palustris (L.) Besser, R. burkartii (Mart.-Laborde) Al-Shehbaz and R. amphibia (L.) Besser; and excludes 3: R. chubutica (O.E.Schulz) Mart.-Laborde, R. pinnata (Sessé & Moc.) Rollins and R. ventanensis Boelcke.

IN BRAZIL Salariato & Zuloaga (Darwiniana, 2020) cites R. bonariensis (Poir.) Macloskie, R. burkartii (Mart.-Laborde) Al-Shehbaz, R. clandestina (Spreng.) J.F. Macbr., R. coxii (F. Phil. ex Phil.) L.E. Navas, R. hilariana (Walp.) Cabrera for Brazil; POWO cites all except R. burkartii and R. coxii, plus R. nana (Schltdl.) J.F. Macbr. (SEE); VPA cites the same all from POWO; Reflora cites all from POWO except R. nana (SEE Reflora). By Species Link, only the three of the Reflora has registered records, and they are the only ones accepted here.

1. Rorippa bonariensis (Poir.) Macloskie. ‣ Ecuador, Peru, Argentina, Paraguay and S Brazil; among the latter country, this species occur only in Rio Grande do Sul state.


2. Rorippa clandestina (Spreng.) J.F. Macbr. ‣ range from Ecuador to Argentina and S Brazil. In Brazil this species ocur in few locations in Paraná, Minas Gerais and Santa Catarina states.


3. Rorippa hilariana (Walp.) Cabrera. ‣ known from Bolivia, Argentina, Paraguay and S Brazil, where occur only in Paraná and Rio Grande do Sul state.


Lorem ipsum dolor sit amet, consectetur adipiscing elit, sed do eiusmod tempor incididunt ut labore et dolore magna aliqua. Ut enim ad minim veniam, quis nostrud exercitation ullamco laboris nisi ut aliquip ex ea commodo consequat. Duis aute irure dolor in reprehenderit in voluptate velit esse cillum dolore eu fugiat nulla pariatur. Excepteur sint occaecat cupidatat non proident, sunt in culpa qui officia deserunt mollit anim id est laborum.

Rorippa clandestina (Spreng.) J.F. Macbr. in Santa Catarina state, Brazil © Species Link/Fototeca Paulo Schwirkowski – FPS

1.2 Tribe Lepidieae - a single genus, Lepidium., recenty incluing Cyphocardamum from Afghanisthan and Lithodraba from Argentina.

C. Lepidium L.

Herbs not scapose; glabrous, pubescent, hirsute, or pilose. Stems usually erect or ascending, sometimes procumbent, decumbent, or prostrate, unbranched or branched. Leaves usually basal and cauline; petiolate or sessile; basal rosulate or not, petiolate (or petiole undifferentiated from blade), blade margins entire, dentate, denticulate, serrate, crenate, or lobed; cauline petiolate or sessile, blade (base auriculate or not), margins entire, dentate, or pinnately divided. Racemes (usually corymbose), elongated or not in fruit. Fruiting pedicels erect to divaricate, slender or stout. Flowers: sepals (usually deciduous, sometimes persistent), usually ovate or oblong, rarely suborbicular; petals (erect or spreading, sometimes rudimentary or absent), obovate, spatulate, oblong, oblanceolate, orbicular, linear, or filiform, claw absent or differentiated from blade, (apex obtuse, rounded, or emarginate); stamens 2 or 4 and equal in length, lateral or median, or 6 and tetradynamous; filaments not dilated basally; anthers ovate or oblong; (ovary placentation apical); nectar glands (4 or 6), distinct, median glands often present. Fruits schizocarps or silicles, (rarely indehiscent), sessile, didymous, oblong, ovate, obovate, cordate, obcordate, elliptic, orbicular, ovoid, obovoid, or globose, strongly angustiseptate or inflated and terete; valves each with prominent veins or not veined, (keeled or rounded, apex winged or not, thin or strongly thickened and ornamented, enclosing or readily releasing seed), glabrous or pubescent; replum rounded, (visible); septum complete or perforated; style absent, obsolete, or distinct, (included or exserted from apical notch); stigma capitate, usually entire, rarely 2-lobed. Seeds oblong or ovate [obovate], plump or flattened, winged, margined, or not winged; seed coat (smooth, minutely reticulate, or papillate), usually copiously mucilaginous when wetted, rarely not; cotyledons usually incumbent (FNA).

DISTRIBUTION subcosmopolitan. 

IN BRAZIL Salariato & Zuloaga (Darwiniana, 2020) cites L. auriculatum Regel & Körn., L. bonariense L. and L. didymum L. in Brazil; VPA cites exactly these three species; POWO (SEE) lists these same three for country; Reflora cites only L. auriculatum Regel & Körn. (as L. aletes J.F.Macbr.) and L. bonariense L. (SEE Reflora).

1. Lepidium auriculatum Regel & Körn. ‣ Peru to S Brazil, Argentina, Chile and Uruguay.


2. Lepidium bonariense L. ‣ collected from Bolivia to SE & S. Brazil, Paraguay, Argentina, Chile and Uruguay.


3. Lepidium didymum L. ‣ native from Peru to S Brazil, Argentina, Chile and Uruguay.


4. Lepidium grandifructum C.L.Hitchc. ‣ known only two collections, endemic to Brazil, known only the type collection from Upper Rio Negro Basin in Paraná state.


Lorem ipsum dolor sit amet, consectetur adipiscing elit, sed do eiusmod tempor incididunt ut labore et dolore magna aliqua. Ut enim ad minim veniam, quis nostrud exercitation ullamco laboris nisi ut aliquip ex ea commodo consequat. Duis aute irure dolor in reprehenderit in voluptate velit esse cillum dolore eu fugiat nulla pariatur. Excepteur sint occaecat cupidatat non proident, sunt in culpa qui officia deserunt mollit anim id est laborum.
 
Lepidium auriculatum Regel & Korn. in Santa Catarina state, Brazil © Species Link/Fototeca Paulo Schwirkowski – FPS
Lepidium bonariense L. in Uruguay © floranativadeuruguay.blogspot.com.br

2. SUPERTRIBE BRASSICODAE

14 tribes, Aphragmeae, Brassiceae, Calepineae, Coluteocarpeae, Conringieae, Eutremeae, Fourraeeae, Isatideae, Kernereae, Plagiolobeae, Schrenkielleae, Sisymbrieae, Thelypodieae, Thlaspideae, 11 absents in South America and three in continent: Coluteocarpeae (3/127), with Noccaea magelanica (Comm. ex Poir.) Holub in Argentina and Chile, Brassiceae (c. 36/c. 275), with Cakile lanceolata (Willd.) O.E. Schulz in Colombia and Venezuela, and the Brazilian Thelypodieae (28/260), widely distributed and exclusively from New World except Pringlea from Prince Edward, Crozet, Kerguélen, and Heard islands.

D. Polypsecadium O.E.Schulz.

Annual or perennial herbs, subshrubs, or shrubs; stems erect to ascending, branched above; basal leaves absent; racemes many flowered, lax, ebracteate, corymbose, elongated considerably in fruit; petals white to lavender or purple, obovate to spatulate, apex obtuse. 

DISTRIBUTION 15 spp., two in N Andes from Colombia and Ecuador, and remaind 12 from Peru to S Argentina (centre of diversity), and one endemic to southern Brazil.

IN BRAZIL Polypsecadium is a very enigmatic genus not recognized in Brazil by the VPA or by Reflora, and has been neglected over the years by scholars in the area.

1. Polypsecadium brasiliense (O.E.Schulz) Al-Shehbaz. ‣ known only the type collection, from Santa Catarina state, no precise location nor collection environment details.


xxx.

June 10, 2023

NEW WORLD ANGIOSPERM ENDEMIC FAMILIES ✅

LAST UPDATED IN 29.09.2024
⋵: 'ENDEMICS'

In old classifications, other families endemic to a country were already recognized as valid. It is the case of Leiteriaceae Benth. (DELTA INTKEY), composed by Leitneria floridana Chapm. and L. pilosa J.A.Schrad. & W.R.Graves, known from Missouri, Arkansas, Texas, Georgia and Florida states in U.S.A., now united within Simaroubaceae (POWO); Duckeodendraceae Kuhlmann (DELTA-INTKEY), known only from Duckeodendron cestroides Kuhlmann, endemic to Amazon forest in Amazonas and Pará states in northern Brazil (GBIF), now under Solanaceae; and and Pterostemonaceae (Engl.) Small (DELTA-INTKEY), known from three species endemics to Mexico, now within Iteaceae (POWO).

Finally, some families are almost endemic of countries, such as Stegnospermataceae Nakai in Mexico (4 spp., all in Meexico, 3 endemics and one up to Central America and Caribbean, POWO), and Rhabdodendraceae Gilg. & Pilg. in Brazil (3 spp., all from Brazil, two endemics and one up to Guianas, Venezuela and Colombia, POWO), both Caryophyllales.

May 28, 2023

BRAZILIAN METAZOA ABSENT LINEAGES ✅

LAST UPDATED IN 29.09.2024
⋵: 'ENDEMICS'

Brazilian 28 absent Metazoa canonic lineages are (1) Xenoturbellida, (2) Nemertodermatida, (3) Filospermoidea, (4) Seisonida, (5) Orthonectida, (6) Rhomboza/Dicyemida, (7) Craniida, (8) Phoronopsis, (9) Monoplacophora, (10) Meiopriapulomorpha, (11) Peripatopsidae, (12) Rhabdopleurida, (13) Asymmetron, (14) Epigonichthys, (15) Hoilungia, (16) Polyplacotoma, (17) Polypodiozoa, (18) Micrognathozoa, (19) Gnosonesimida, (20) Haplopharyngida, (21) Cycliophora, (22) Loxokalypodida, (23) Mesotardigrada, (24) Remipedia, (25) Petromyzontii, (26) Cladistii, (27) Coelacantha and (28) Rhynchocephalia (Brazilian Metazoa, 2023).

BRAZILIAN ABSENT PHYLLA WORLDWIDE, INCLUDING PHYLOGENETIC ISSUES

Nine are monotypics., three are diotypics (Coelacantha 1:1/2 Loxokalypodida 1:1/2 and Cycliophora 1:1/2) and remaining from 3 to 127 spp.: Peripatopsidae (1:41/127), Dicyemida, (3:9/115), Petromyzontii (3:10/48), Monoplacophora (4:8/30), Remipedia (8:12/28), Filospermoidea (2:3/28), Orthonectida (2:5/26), Cladistii (1:2/14), Meiopriapulomorpha (1:1/12), Craniida (1:3/11), Nemertodermatida (2:6/9), Xenoturbelllida (1:1/6), Gnosonesimida (1:1/6), Rhabdopleurida (1:1/5), Seisonida (1:2/4), Phoronopsis (1:1/3) and Haplopharyngida (1:1/3).

Joined, these groups has (46:119/)493 spp.

FULL MAP OF RANGE OF ALL BRAZILIAN METAZOA LINEAGES (UPDATED IN 10 MAR, 2024)

May 25, 2023

ANIMAL OUTER FAMILIES NEAR BRAZIL

LAST UPDATED IN 29.09.2024

Two mammal families was collected near Brazilina borders, and maybe collected also in country. Both was collected in NE Argentina, near Brazilian border at western bank of Uruguay river, in Rio Grande do Sul state. Lagostomus maximus Desmarest, 1817, belong to rodent family Chinchilidae, a family absent in Brazil, and also occur in Bolivia and Paraguay; Chacodelphys formosa Shamel, 1930, is a marsupial from Didelphidae family, and is a endemic genus for Argentina.

ARGENTINAN RANGE OF LAGOSTOMUS (BLUE DOTS, ECOREGISTROS) AND CHACODELPHYS (PINK DOTS, TETA & PARDINAS, 2007, SEE)

May 17, 2023

SMALLEST VERTEBRATES FROM BRAZIL✅

LAST UPDATED IN 29.09.2024
⋵: 'ENDEMICS'

Brazil is the world's hotspot for miniaturized Craniata, with the smallest members of Squamata, Amphibian and Actinopterigii from across continental America being endemic to Brazil. More than that, our smallest Amphibia and Actinopterigii are the smallest in the entire Western Hemisphere and are among three of their groups worldwide. The smallest Brazilian Squamata is second in New World only to some nanolizards in the Caribbean on the continent.

Actinopterigii ▸ two of the three smallest Actinipterigii are two Brazilian species from endemic genus Leptophilypnion (Eleotridae): L. fittkaui T. R. Roberts, 2013 known only from Rio Negro in Amazonas state, and L. pusillus T. R. Roberts, 2013 known only from Tapajós River in Pará state (Roberts et al., Intenational Journal of Ichthyology, 2013), with mature lengts of 9.1 to 9,3mm. Over a hundred of Neotropical fishes run as miniaturized, with mature age below 26mm (Piza et al., Neotropical Ichtyology, 2014).

Amphibia ▸ Brachycephalus pulex Napoli, Caramaschi, Cruz & Dias, 2011, found only in southern Bahia, may be even smaller, with adults measuring just 7.1 mm on average, 1 mm lesser Paedophryne amauensis from Papua New Guinea, being the smallest known vertebrate for several sources (Revista Fapesp).

Squamata ▸ smallest Squamata from Brazil and South America, possibly in mainland New World, is Coleodactylus natalensis Freire 1999 (Sphaerodactylidae), known only from remants of Atlantic Forest in Rio Grande do Norte state, NE Brazil, with males and females reach a maximum snout-vent length of 22 and 24 mm (Lisboa, Sales & Freire, Zoologia, 2012). Other species in this genus are very small, and are distributed from Venezuela, Guianas and Brazil except southern parts. Miniaturized lizards also occur in Gymnophthalmidae.

April 21, 2023

MÚSICAS 1: BAHIA, ANOS 90

1. PROTESTO DO OLODUM (Bamda Mel)

Moçambique hey, por minuto alguém vai morrer, sem ter pão nem água para beber....


2. MADAGASCAR (Banda Reflexu's)

Ilha, ilha do mor, Madagascar


3. SENEGAL (Banda Reflexu's)

Diz povão, Senegal região. 
 


4. BAGDÁ (Bamda Mel)

Oooh, Bagdá, Oooh Bagdá, Ooooooh, Bagdá 
 

February 18, 2023

AS MAIORES FALÉSIAS DO BRASIL

Os mais significativos sistemas de falésias do Brasil estão nos estados do Ceará (praias do Morro Branco e das Fontes, em Beberibe; Canoa Quebrada, em Aracati; e Redonda, em Icapuí), no Rio Grande do Norte (no município de Touros e na Praia da Pipa, em Tibau do Sul), Paraíba (Ponta do Seixas, em João Pessoa), Alagoas (Praia do Gunga), Bahia (Costa da Praia Dourada, em Mucuri), São Paulo e Rio Grande do Sul (falésias de Torres), conforme Saiba Mais (2021).

Com o objetivo de listar o mais longo sistema contínuo (paredão extenso sem ser interrompido por cursos d'água) da costa brasileira, o Almanaque Z, usando a ferramnta de comprimento do Google Earth, calculou suas extensões lineares, com leve contorno, da extensão de cada uma.

RESULTADO

Todos os sistemas citados acima têm menos de 1200m de extensão com exceção de Beberibe (CE), Touros (RN), da Ponta do Seixas (PB), do Gunga (AL) e da Costa Dourada (BA), sendo estes indubitavelmente os mais longos o país. Apenas um dos trechos da Costa Dourada superaram 2,5 km, chegando a cerca de 2,7 km. O Almanaque Brazil considera, assim, esta a mais longa falésia contínua do Brasil, em comprimento.


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SEE ALSO

QUAL A MAIOR DOLINA DO BRASIL?
DEEPEST POINT OF BRAZILIAN ATLANTIC

February 17, 2023

NOCTILUCA NO BRASIL

LAST UPDATED IN 29.09.2024

No Brasil os registros de bioluminescência por Noctiluca são entremamente vagos, imprecisos e não documentados cientificamente. Mundo afora, como fenômeno biológico, os bloons deste protista na noite são fartamente documentados, conhecidos e alguns descritos em artigos científicos.

As noctilucas, precisamente Noctiluca scintillans (Macartney) Kofoid & Swezy, são dinoflagelados da família Noctilucaceae, que ocorrem em todo o mundo; eles produzem luz em flashes como resultado da reação entre luciferina e luciferase, durante estresse mecânico, por isso sua presença é notada em águas agitadas próximo das costas (Wikipedia).

Abaixo, um checklist de registros de bioluminescência de Noctiluca no Brasil, feito em busca rápida pela internet.

  • registro na praia do Ervino, São Francisco do Sul, em 18 de julho de 2024 (NSC Total).
  • registro feito em Balneário Camboriú, também em 18 de julho de 2024 (G1, com vídeo).
  • registro em 28 de julho de 2023, em um clube de canoagem na Baía Norte em Florianópolis às 6h15 (G1, com vídeo).
  • registro em vídeos em Capão da Canoa (RS), em janeiro de 2022, dois links (Youtube Link 1, Youtube Link 2).
  • registro na região de Torres (RS) por Gabriel Zaparolli em outubro de 2021, publicado pelo Olhar Digital (LINK) e o Met Sul (LINK).
  • registro no litoral norte do Rio Grande do Sul, citado em Souza Cardoso (Brazilian Journal of Oceanography, 2012), como um registro jornalístico do Zero Hora, sem mais detalhes.
  • registros de ocorrência, curiosamente com tons de extrema ordinaridade, na Ilha do Mel (PR), por JB Litoral (LINK), com um texto com falas de especialistas mas sem registros de foto ou vídeo fiáveis.
  • citações, sem nenhum detalhe, de ocorrência também na Ilha do Cardoso (SP), em Desviantes (LINK).

BIOLUMINESCÊNCIA DE NOCTILUCA EM CAPÃO DA CANOA, RS


February 15, 2023

POST AVULSO: UMA PLANTA ESTRANHA

Por muito tempo uma árvore bastante alongada, plantada na frente de uma concessionária da mais importante avenida de Teresina, Piauí, chamava a atenção pelo seu aspecto. Por mais que este autor que vos fala tivesse curiosidade de saber que espécies era aquela, jamais fez nada para entender. Na sua ignorância, apenas supeitava que era uma Araliaceae, talvez relatado a Schefflera.

Um dia, vasculhando o site Flora of the World, autor enontrou a planta. Ali. Magnifica. Não era uma Schefflera. Não era Araliaceae. Nem Apiales. Nem Eudicots mesmo era. Era, de modo bastante inesperado, uma Annonaceae!! Monoon longifolium (Sonn.) B.Xue & R.M.K.Saunders, antiga Polyalthia longifolia (Sonn.) Benth. & Hook.f. ex Thwaites, nativa da Índia e Sri Lanka. Mistério resolvido.

February 06, 2023

CUSHIONS OF SOUTH AMERICA (EXCEPT BRAZIL)

INTRODUCTION

Cushion plants represent a special life form which usually has character combinations such as short-node intervals, compact branches, solitary flowers or few-flowered racemes, and dome- or mat-shaped cushions. They are common among perennial herbs growing on high-altitude mountains and are thought to be associated with dry and cold environments, such as the high Andes and Patagonia, Himalayas, and New Zealand Alps. Aubert et al. (Alpine Botany, 2014) updated the cushion plants catalogue in which they recognized 1,309 species of 63 families and 273 genera.

This post aims to list the cushions from South America in light of new molecular and distributional data. The primary list follows Alpine Cushions (SEE), but with due corrections via POWO (SEE); names assigned to a country in Alpine Cushions but not assigned in the VPA are in salmon color; the reverse situation (which are all accepted here) is marked in blue.

In this compilation we list 280 cushions in 86 genera at 38 families among 20 orders, 18 if them in Eudicots. By country, the diversities are Venezuela (21 spp. in 12 genera at 10 families), Colombia (38 spp. in 20 genera at 13 familes), Ecuador (53 spp. in 28 genera at 18 families), Peru (72 spp. in 35 genera at 22 families), Bolivia (64 spp. in 34 genera at 22 families), Argentina (194 spp. in 67 genera at 31 families), and Chile (158 spp. in 59 genera at 30 families). Gentianaceae, Malvaceae and Saxifragaceae occur only from Ecuador southwards. Fabaceae, Lamiaceae, Verbenaceae and Frankeniaceae occur only from Peru southwards; Oxalidaceae and Bromeliaceae occur only in Bolivia southwards. Restionaceae, Iridaceae, Asteliaceae, Rosaceae, Violaceae, Thymelaeaceae, Plumbaginaceae, Montiaceae, Solanaceae, Rubiaceae occur only in Argentina and Chile; Loasaceae only in Chile.

Cushions of South America

The Top 5 genera (Azorella, Nototriche, Junellia, Pycnophyllum and Benthamiella) composes more than 1/3 of all cushions in South America (90 spp). None of them occur in Brazil. Taxonomic changes: Phyllactis and Aretioides under Valeriana; Petunia under Fabiana; Mulinum under Azorella; Belloa under Mniodes; Deuterocohnia under Dyckia.

Some claims for cushions in South America are not on this list. Jalcophila M.O. Dillon & Sagást. and Aphanactis Wedd. in Asteraceae (K.Kubitzki, vol. VIII, 2007); Englerocharis Musch. (Brassicaceae) from Peru (Al-Shehbaz et al., Kew Bulletin, 2012); Gamocarpha DC. and Moschopsis Phil. (Calyceraceae) from Chile and Argentina (Pozner & al., Taxon, 2021). Ribes frankei Weigend & Breitkopf (Grossulariaceae), endemic to mountains of Peru, is the unique cushion-like species among this family (Weigend ey al., Novon, 2010).

Although there is no citation in the literature, many species of Poales do Brazil could be considered cushions, within the current limits adopted, namely Paepalanthus glabrifolius Ruhland, P. pseudotortilis Ruhland, Leiothrix plantago (Mart.) Giul. and L. curvifolia Ruhland (Eriocaulaceae), Abolboda killipii Lasser and A. americana (Aubl.) Lanj. (Xyridaceae); all of these are endemic to Brazil except the Abolboda Bonpl., which extend into the adjacent countries of the Guiana Shield. In Mexico there are only 13 cushions in 6 genera of two families: Cactaceae with Echinocereus (2), Epitelantha (1), Ferocactus (1), and Mammilaria (7), and Caryophyllaceae with Arenaria bryoides and Colobanthus quitensis.

TAXONOMY

IRIDACEAE ‣ Tapeinia pumila (G.Forst.) Baill. (AR, CH).

ASTELIACEAE ‣ Astelia pumila (J.R.Forst.) Gaudich. (AR, CH).

RESTIONACEAE ‣ Gaimardia australis Gaudich. (AR, CH).

BROMELIACEAE ‣ Dyckia grisebachii Baker (BL, AR syn. Deuterocohnia brevifolia, inc. Deuterocohnia lorentziana).

ERIOCAULACEAE ‣ Paepalanthus karstenii Ruhland (VZ, CL, EC, PR, BL), P. ferreyrae Moldenke (PR), P. lodiculoides Moldenke (VZ, CL, EC, PR), P. pilosus (Kunth) Kunth (VZ, CL, EC, PR), P. stegolepoides Moldenke (VZ); for pulvinate species in northern Andes, see Hensold (PhytoKeys, 2016).

JUNCACEAE ‣ Distichia acicularis Balslev & Laegaard (EC), D. filamentosa Buchenau (PR, BL, CH), D. muscoides Nees & Meyen (CL, EC, PR, BL, AR, CH), Oxychloe andina Phil. (PR, BL, AR, CH), O. bisexualis Kuntze (AR, CH), O. castellanosii Barros (AR), O. haumaniana (Barros) Barros (AR, CH), O. mendocina Barros (AR), Patosia clandestina (Phil.) Buchenau (BL, AR).

Juncaceae chart
Distichia muscoides Nees & Meyen, D. filamentosa Buchenau, Oxychloe andina Phil.

CYPERACEAE ‣ Carpha alpina R.Br. (CH), Oreobolus cleefii L.E.Moro (CL, EC, PR), O. ecuadorensis T.Koyama (CL, EC, PR), O. goeppingeri Suess. (VZ, CL, EC, PR, BL), O. obtusangulus Gaudich. (VZ, CL, EC, PR, BL, CH), O. venezuelensis Steyerm. (VZ, CL, EC, PR, BL), Rhynchospora oreoboloidea Gómez-Laur. (CL, EC), Phylloscirpus deserticola (Phil.) Dhooge & Goetgh. (EC, PR, BL, AR, CH), Zameioscirpus atacamensis (Phil.) Dhooge & Goetgh. (PR, BL, AR), Z. gaimardioides (É.Desv.) Dhooge & Goetgh. (PR, AR, CH), Z. muticus Dhooge & Goetgh. (PR, BL, AR, CH); for range in northern Andes, see Springer Nature (LINK).

Cyperaceae chart
Oreobolus obtusangulus Gaudich., Zameioscirpus atacamensis (Phil.) Dhooge & Goetgh.

XYRIDACEAE ‣ Xyris subulata Ruiz & Pav. (GU, VZ, CL, EC, PR).

POACEAE ‣ Aciachne pulvinata Benth. (VZ, CL, EC, PR, BL), A. acicularis Laegaard (VZ, CL, EC, PR, BL, AR), A. flagellifera Laegaard (CL, EC), Deschampsia venustula Parodi (AR, CH).

Aciachne chart
Aciachne pulvinata Benth., A. acicularis Laegaard

RANUNCULACEAE ‣ Caltha appendiculata Bercht. & J.Presl (AR, CH), C. sagittata Cav. (EC, PR, BL, CH).

Caltha card

SAXIFRAGACEAE ‣ Saxifraga magellanica Poir. (EC, PR, BL, AR, CH, inc. S. adenodes Poepp. ex Sternb.), Saxifragella bicuspidata (Hook. f.) Engl. (AR, CH).

Saxifraga magellanica
Saxifraga magellanica Poir.

FABACEAE ‣ Adesmia aconcaguensis Burkart (AR), A. aegiceras Phil. (AR, CH), A. ameghinoi Speg. (AR), A. aueri Burkart (AR), A. caespitosa Phil. (AR, CH), A. digitata Burkart (AR), A. echinus C.Presl (AR, CH), A. erinacea Phil. (BL, AR, CH), A. frigida Phil. (CH), A. glomerula Clos (AR, CH), A. neglecta M.N.Correa (AR), A. horrida Hook. & Arn. (BL, CH), A. occulta (R.E.Fr.) Burkart (PR, BL, CH), A. pentaphylla Phil. (AR, CH), A. salicornioides Speg. (AR, CH), A. serrana M.N.Correa (AR), A. subterranea Clos (AR, CH), Anarthrophyllum burkartii Soraru (AR), A. desideratum (DC.) Benth. (AR, CH), A. gayanum (A.Gray) B.D.Jacks. (AR, CH), A. patagonicum Speg. (AR).

Adesmia erinacea Phil., A. occulta (R.E.Fr.) Burkart

OXALIDACEAE ‣ Oxalis compacta Gillies ex Hook. & Arn. (AR), O. erythrorrhiza Gillies ex Hook. & Arn. (AR), O. holosericea Phil. (CH), O. hypsophila Phil. (BL, CH, AR), O. loricata Dusén (AR), O. muscoides Phil. (AR).

Oxalis hypsophila Phil.

ROSACEAE ‣ Acaena alpina Poepp. ex Walp. (AR, CH), A. caespitosa Gillies ex Hook. & Arn. (AR, CH), A. confertissima Bitter (AR), A. lucida Vahl (AR, CH).

VIOLACEAE ‣ Viola auricolor Skottsb. (AR, CH), V. dasyphylla W.Becker (AR).

THYMELAEACEAE ‣ Drapetes muscosus Hook.f. (AR, CH).

BRASSICACEAE ‣ Brayopsis colombiana Al-Shehbaz (CL, EC), B. calycina (Desv.) Gilg & Muschl. (PR, BL, AR), B. diapensioides (Wedd.) Gilg & Muschl. (PR, BL), Dactylocardamum imbricatifolium Al-Shehbaz (PR), Delpinophytum patagonicum (Speg.) Speg. (AR), Draba aretioides Humb. & Bonpl. ex DC. (EC), D. depressa Hook.f. (CL, EC, PR), D. gilliesii Hook. & Arn. (AR, CH), D. obovata Benth. (EC), Eudema nubigena Humb. & Bonpl. (EC), E. hauthalii Gilg & Muschl. (AR, CH), E. werdermannii O.E.Schulz (AR, CH), Lithodraba mendocinensis (Hauman) Boelcke (AR), Onuris hatcheriana (Gilg ex Macloskie) Gilg & Muschl. (AR, CH), Physaria okanensis Al-Shehbaz & Prina (AR), Xerodraba colobanthoides Skottsb. (AR), X. glebaria (Speg.) Skottsb. (AR), X. lycopodioides (Speg.) Skottsb. (AR), X. monantha (Gilg ex Kuntze) Skottsb. (AR), X. patagonica (Speg.) Skottsb. (AR, CH), X. pectinata Skottsb. (AR, CH), X. pycnophylloides (Speg.) Skottsb. (AR).

Draba depressa Hook.f., Dactylocardamum imbricatifolium Al-Shehbaz

Brayopsis colombiana Al-Shehbaz, Eudema nubigena Humb. & Bonpl.

GERANIACEAE ‣ Geranium crassipes Hook. ex A.Gray (CL, PR), G. sericeum Willd. ex Spreng. (EC).

Geranium sericeum Willd. ex Spreng.

MALVACEAE ‣ Nototriche azorella Hill (PR, CH), N. auricoma A.W. Hill (CH), N. compacta A.W. Hill (PR).

, CH, AR, CH), N. ecuadoriensis Fryxell (EC), N. flabellata (Wedd.) A.W. Hill (PR, BL), N. holoserica A.W. Hill (AR, CH), N. jamesonii A.W.Hill (EC, syn. N. hartwegii A.W. Hill), N. obcuneata (Baker f.) A.W. Hill (PR, BL, CH), N. orbignyana (Wedd.) A.W. Hill (PR, BL, CH), N. parviflora A.W. Hill (AR, CH), N. pediculariifolia (Meyen) A.W. Hill (PR, BL, CH), N. philippii A.W. Hill (AR, CH), N. phyllanthos (Cav.) A.W. Hill (EC, PR, inc. N. pichinchensis (Bonpl.) A.W. Hill), N. polygama Krapov. (BL), N. pulvilla A.W. Hill (AR), N. sajamensis (Hieron.) A.W. Hill (PR, BL), N. stipularis (Phil.) A.E.Martic. (BL, CH), N. turritella A.W. Hill (PR, BL, CH).

Nototriche compacta A.W. Hill, Nototriche obcuneata (Baker f.) A.W. Hill, Nototriche phyllanthos (Cav.) A.W. Hill

FRANKENIACEAE ‣ Frankenia triandra Remy (PR, BL, AR, CH; inc. Pycnophyllum pilgerianum Muschl).

Frankenia triandra Remy

PLUMBAGINACEAE ‣ Armeria curvifolia Bertero (AR, CH), A. maritima Willd. (AR, CH).

MONTIACEAE ‣ Calandrinia caespitosa Gillies ex Arn. (AR), C. colchaguensis Barnéoud (AR), C. ferruginea Barnéoud (CH), C. potentilloides Barnéoud (AR), C. sericea Hook. & Arn. (AR).

CACTACEAE ‣ Airampoa soehrensii (Britton & Rose) Lodé (PR, BL, CH, inc. Tunilla soehrensii (Britton & Rose) D.R. Hunt & Iliff), Austrocylindropuntia floccosa (Salm-Dyck ex Winterfeld) F.Ritter (PR, BL), Copiapoa ahremephiana N.P.Taylor & G.J.Charles (CH), C. cinerascens (Salm-Dyck) Britton & Rose (CH), C. dealbata F.Ritter (CH), C. longistaminea F.Ritter (CH), C. solaris (F.Ritter) F.Ritter (CH), Cumulopuntia boliviana (Salm-Dyck) F.Ritter (PR, BL, AR, CH; inc. Maihueniopsis bolivianum (Salm-Dyck) R. Kiesling and M. pentlandii (Salm-Dyck) R. Kiesling), Gymnocalycium monvillei (Lem.) Pfeiff. ex Britton & Rose (AR), M. glomerata (Haw.) R. Kiesling (BL, AR, CH), Opuntia atacamensis Phil. (CH).

Austrocylindropuntia floccosa (Salm-Dyck ex Winterfeld) F.Ritter, Cumulopuntia boliviana (Salm-Dyck) F.Ritter, Tunilla soehrensii (Britton & Rose) D.R. Hunt & Iliff

CARYOPHYLLACEAE ‣ Arenaria bisulca (Bartl.) Fenzl ex Rohrb. (PR, AR), A. denticulata Phil. (CH), A. dicranoides Kunth (VZ, EC, PR, BL), A. musciformis Triana & Planch. (VZ, CL, EC), A. venezuelana Briq. (VZ, CL), Colobanthus quitensis (Kunth) Bartl. (CL, EC, PR, BL, CH), C. lycopodoides Griseb. (AR, CH), C. subulatus (d'Urv.) Hook.f. (AR, CH), Paronychia sessiliflora Nutt. (BL), Pycnophyllum argentinum Pax (BL, AR), P. bryoides (Phil.) Rohrbach (PR, BL, AR, CH), P. glomeratum Mattf. (PR, AR, CH), P. macropetalum Mattf. (PR, BL, AR, CH), P. mattfeldii J.F. Macbr. (PR, BL), P. molle Remy (CL, PR, BL, AR, CH), P. spathulatum Mattf. (BL, CH), P. stuebelii Mattf. (BL), P. tetrastichum Remy (PR, BL, AR, CH, inc. P. kobalanthum Mattf.), P. muscosa Skottsb. (AR), P. convexum Griseb. (AR), P. mucronulatum Mattf. (AR), Philippiella patagonica Speg. (AR, CH), Reicheella andicola (Phil.) Pax (CH), Silene haumanii Bocquet (AR).

Arenaria bisulca (Bartl.) Fenzl ex Rohrb., A. dicranoides Kunth, A. musciformis Triana & Planch.

Pycnophyllum bryoides (Phil.) Rohrbach, P. molle Remy

Colobanthus quitensis (Kunth) Bartl.

LOASACEAE ‣ Loasa caespitosa Phil. (CH).

ERICACEAE ‣ Disterigma empetrifolium (Kunth) Nied. (VZ, CL, EC, PR, BL).

Disterigma empetrifolium (Kunth) Nied.

GENTIANACEAE ‣ Gentianella armerioides (Griseb. ex Gilg) J.S.Pringle (PR, BL), Halenia minima C.K. Allen (EC), Halenia pusilla Gilg (PR, BL).

Halenia minima C.K. Allen

RUBIACEAE ‣ Oreobolus obtusangulus Gaudich. (AR), O. glacialis (Poepp.) Ricardi (AR, CH).

SOLANACEAE ‣ Benthamiella azorella (Skottsb.) C.Soriano (AR), B. azorelloides Speg. (AR, CH), B. chubutensis C.Soriano (AR), B. graminifolia Skottsb. (AR), B. lanata C.Soriano (AR), B. longifolia Speg. (AR), B. nordenskjoldii Dusén (AR), B. patagonica Speg. (AR, CH), B. pycnophylloides Speg. (AR), B. skottsbergii C.Soriano (AR), B. sorianoi S.Arroyo (AR), B. spegazziniana C.Soriano (AR, CH), Combera minima Sandwith (CH), Fabiana australis Alaria (AR), F. foliosa (Speg.) S.C.Arroyo (AR), F. nana (Speg.) S.C.Arroyo (AR), Pantacantha ameghinoi Speg. (AR).

CALCEOLARIACEAE ‣ Calceolaria mendocina Phil. (AR, CH), C. pennellii Descole & Borsini (AR), C. pinifolia Cav. (AR, CH), C. prichardii (Rendle) Kraenzl.

LAMIACEAE ‣ Hedeoma mandoniana Wedd. (PR, BL, AR).

Hedeoma mandoniana Wedd.

PLANTAGINACEAE ‣ Plantago barbata G.Forst. (AR, CH), P. rigida Kunth (VZ, CL, EC, PR, BL), P. sempervivoides Dusén (AR, CH), P. tubulosa Decne (VZ, EC, PR, BL), P. uniglumis Wallr. ex Walp. (AR, CH).

Plantago rigida Kunth, P. tubulosa Decne 

VERBENACEAE ‣ Junellia aretioides (R.E.Fr.) Moldenke (BL, AR, CH), J. azorelloides (Speg.) Moldenke (AR), J. caespitosa (Gillies & Hook., CH) Moldenke (AR), J. congesta (Tronc.) Moldenke (AR), J. digitata (Phil.) Moldenke (BL, CH, AR, CH), J. erinacea (Gillies & Hook.) Moldenke (AR), J. micrantha (Phil.) Moldenke (CH), J. minima (Meyen) Moldenke (PR, BL, AR), J. mulinoides (Speg.) Moldenke (AR), J. odonellii Moldenke (AR, CH), J. pappigera (Phil.) N. O'Leary & P. Peralta (AR, CH), J. patagonica (Speg.) Moldenke (AR, CH), J. silvestrii (Speg.) Moldenke (AR, CH), J. toninii (Kuntze) Moldenke (AR, CH), J. uniflora (Phil.) Moldenke (AR, CH).

Junellia minima (Meyen) Moldenke 

ASTERACEAE ‣ Abrotanella diemii Cabrera (AR), A. emarginata (Cass. ex Gaudich.) Cass. (AR, CH), A. linearifolia A.Gray (CH), A. purpurea Swenson (AR, CH), A. submarginata A.Gray (CH), A. trichoachaenia Cabrera (AR, CH), A. trilobata Swenson (AR, CH), Baccharis aretioides Turcz. (EC), Brachyclados caespitosus (Phil.) Speg. (AR), Belloa chilensis Remy (BL, AR, CH), Burkartia lanigera (Hook. & Arn.) Crisci (AR), Chuquiraga aurea Skottsb. (AR), Erigeron leptopetalus Phil. (AR, CH), E. rosulatus Wedd. (PR, BL, AR, CH), Gamochaeta nivalis Cabrera (AR,CH), Lucilia kunthiana (DC.) Zardini (VZ, CL, EC, PR, BL), Mniodes aretioides Cuatrec. (PR, BL), M. caespititia (Wedd.) Quip. & M.O.Dillon (BL), M. longifolia (Cuatrec. & Aristeg.) Sagást. & M.O.Dillon (VZ, CL, EC, PR, BL), M. radians (Benth.) Sagást. & M.O.Dillon (VZ, CL, EC), M. schultzii (Wedd.) S.E.Freire, Chemisquy, Anderb. & Urtubey (EC, PR, BL, AR, CH inc. M. virescens (Wedd.) Cabrera), Monticalia microdon (Wedd.) B.Nord. (EC), Nardophyllum bryoides (Lam.) Cabrera (AR, CH), Nassauvia ameghinoi Speg. (AR), N. pentacaenoides Speg. (AR), Raouliopsis pachymorpha (Wedd.) S.F.Blake (CL), R. seifrizii S.F.Blake (CL), Senecio culcitenellus Cuatrec. (AR, CH), S. depressus Hook. & Arn. (AR, CH), S. digitatus Phil. (AR, CH), S. skottsbergii Cabrera (AR, CH), S. subdiscoideus Sch.Bip. ex Wedd. (PR, BL, AR, CH), Werneria aretioides Wedd. (PR, BL, AR, CH), W. humilis Kunth (CL, EC, PR, BL), W. poposa Phil. (PR, BL, AR), W. pumila Kunth (CL, EC, PR, AR), W. pygmaea Gillies ex Hook. & Arn. (VZ, CL, EC, PR, BL, CH), W. rosea Hieron. (EC), Xenophyllum incisum (Phil.) V.A.Funk (AR, CH), X. pseudodigitatum (Rockh.) V.A.Funk (AR, CH).

Erigeron rosulatus Wedd. and Werneria aretioides Wedd.

Mniodes schultzii (Wedd.) Cabrera, Senecio subdiscoideus Sch.Bip. ex Wedd., Xenophyllum humile (Kunth) V.A.Funk

STYLIDIACEAE ‣ Donatia fascicularis J.R.Forst. & G.Forst. (AR, CH), Phyllachne uliginosa J.R. Forst. & G. Forst. (AR, CH).

CAMPANULACEAE ‣ Lysipomia aretioides Kunth (EC, PR), L. muscoides Hook.f. (CL, EC, PR).

Lysipomia muscoides Hook.f.

CAPRIFOLIACEAE ‣ Valeriana alypifolia Kunth (EC), V. aretioides Kunth (EC, PR, BL), V. corynodes Borsini (AR), V. densa (Wedd.) Höck (BL), V. macrorhiza Poepp. ex DC. (BL, AR, CH), V. rigida Ruiz & Pav. (CL, EC, PR, BL), V. sedifolia d'Urv. (AR, CH, inc. Aretiastrum magellanicum (Decne.) Skottsb.).

Valeriana rigida Ruiz & Pav.

APIACEAE ‣ Azorella albovaginata (Gillies & Hook.) G.M.Plunkett & A.N.Nicolas (AR, CH), A. ameghinoi Speg. (AR, CH), A. aretioides (Kunth) Willd. ex DC. (CL, EC, PR, AR), A. biloba (Schltdl.) Wedd. (CL, EC, PR, BL, AR, CH), A. corymbosa (Ruiz & Pav.) Pers. (CL, EC, PR), A. compacta Phil. (PR, BL, AR, CH), A. crassipes Phil. (AR, CH), A. crenata (Ruiz & Pav.) Pers. (VZ, CL, EC, PR), A. diapensioides A.Gray (PR, BL, AR, CH), A. diversifolia Clos (AR, CH), A. filamentosa Lam. (AR, CH), A. fuegiana Speg. (AR, CH), A. hallei (Skottsb.) G.M.Plunkett & A.N.Nicolas (AR), A. julianii Mathias & Constance (VZ, CL), A. lycopodioides Gaudich. (AR, CH), A. madreporica Clos (AR, CH), A. microphylla (Cav.) G.M.Plunkett & A.N.Nicolas (AR), A. monantha Clos (AR, CH), A. multifida (Ruiz & Pav.) Pers. (VZ, CL, EC, PR, BL), A. nivalis Phil. (AR, CH), A. patagonica Speg. (AR, CH), A. pectinata Phil. (CH), A. pedunculata (Spreng.) Mathias & Constance (CL, EC), A. pulvinata Wedd. (PR, BL), A. prolifera (Cav.) G.M.Plunkett & A.N.Nicolas (AR, CH), A. ruizii G.M.Plunkett & A.N.Nicolas (AR, CH), A. selago Hook.f. (AR, CH), A. spinosa (Ruiz & Pav.) Pers. (AR, CH), A. trifoliolata Clos (AR, CH), A. trifurcata (Gaertn.) Pers. (AR, CH), A. trisecta (H.Wolff) Mart.Fernández & C.I.Calviño (BL, AR, CH; syn. Mulinum crassifolium), A. valentini (Speg.) Mart.Fernández & C.I.Calviño (AR, CH), Bolax caespitosa Hombr. & Jacquinot ex Decne (AR, CH), B. gummifera (Lam.) Spreng. (AR, CH).

Azorella compacta Phil., A. diapensioides A.Gray