Aloe maculata subsp. maculata
Authors/Creators
- 1. Ria Olivier Herbarium, Department of Botany, Nelson Mandela University, P. O. Box 77000, Gqeberha, 6031 South Africa. & smithgideon 1 @ gmail. com; https: // orcid. org / 0000 - 0002 - 5417 - 9208
- 2. Ria Olivier Herbarium, Department of Botany, Nelson Mandela University, P. O. Box 77000, Gqeberha, 6031 South Africa. & epnfigueiredo @ gmail. com; https: // orcid. org / 0000 - 0002 - 8511 - 8213
- 3. Meise Botanic Garden, Nieuwelaan 38, B- 1860 Meise, Belgium. & filip. verloove @ plantentuinmeise. be; https: // orcid. org / 0000 - 0003 - 4144 - 2422
- 4. Foundational Biodiversity Science Division, South African National Biodiversity Institute, Private Bag X 101, Pretoria, 0001 South Africa. & H. G. W. J. Schweickerdt Herbarium, Department of Plant and Soil Sciences, University of Pretoria, Pretoria, 0002 South Africa.
- 5. Centre for Applied Ecology Prof. Baeta Neves, School of Agriculture, University of Lisbon, Tapada da Ajuda, 1349 - 017 Lisbon, Portugal. & Egas Moniz Center for Interdisciplinary Research (CiiEM), Egas Moniz School of Health and Science, Campus Universitário, Quinta da Granja, Monte da Caparica, 2829 - 511 Caparica, Portugal.
Description
2. Aloe maculata Allioni (1773: 65 [13]) subsp. maculata (Fig. 2).
Locally used synonyms:— Aloe saponaria (Aiton 1789: 467) Haworth (1804: 17).
Common name(s):— Portuguese: áloe-manchado. English: soap aloe (Grace et al. 2011).
Description:—Plants acaulescent or with stem up to 0.5 m tall; rosettes solitary or suckering to form dense groups. Leaves densely rosulate, erectly spreading to slightly recurved, up to 25–30 × 8–12 cm, ovate-lanceolate, with dried twisted apex, adaxial surface pale to darker green, with numerous, dull, H-shaped or irregularly shaped, white maculations in irregular broken, wavy, transverse bands, abaxial surface paler green, obscurely lineate and usually without maculations; margin horny, brown; marginal teeth ± 10 mm apart, 3–5 mm long, pungent, reddish brown; exudate clear. Inflorescence 0.4–1.0 m high, erect, branched. Racemes 10–12 cm long, capitate-corymbose, dense. Floral bracts ± 12–23 × 3–5 mm. Pedicels 35–45 mm long. Flowers: perianth 35–50 mm long, up to 10 mm across ovary, abruptly constricted above ovary to form sub-globose basal swelling, enlarging towards wide open mouth, slightly decurved, usually salmon pink to orange; outer segments free for 10–15 mm; stamens exserted 1–3 mm; style exserted to 5 mm. Capsule (2.0–)2.5–3.0 cm long, oblong.
Flowering time:—April–July.
Habitat:—On old (stone) walls and in abandoned gardens (Almeida 2012: 209). A range of sites in natural vegetation, including on coastal cliffs and sand dunes.
First mention of the species as naturalised in Portugal:—1998 (fide Almeida & Freitas 2006: 119).
Localities recorded:— Almeida (2012: 209, as “ Aloe saponaria ”) recorded it as casual in BL (Alhadas) and Ag (Sagres). Güemes (2013: 314) recorded it for E (Serra d’El Rei), BAl, and Ag. Silva et al. (2015: 69–70, 75) recorded it as casual and escaped at Cascais, Oeiras, north of Lisbon. It is here recorded at the following further localities; São João do Estoril (E); Almograve, Porto Covo (BAl), Cabo de Sagres (Ag).
Country / region of origin:—Southern Africa. It occurs from the Cape Peninsula through the provinces of Western and Eastern Cape, into the eastern Free State, through KwaZulu-Natal to Mpumalanga, South Africa, as well as in Lesotho and Eswatini.
Secondary distribution range:— Aloe maculata is very sparingly naturalised in areas with a Mediterranean climate. It is reportedly known as such from the western Mediterranean area: France (Provence and Corsica; Tison & de Foucault 2014), Spain (Guillot Ortiz et al. 2008, Aymerich & Sáez 2019), Gibraltar (Lamb 1996), and Malta (Mifsud 2022; erroneously as ‘ A. microstigma subsp. microstigma ’). In Italy, it is a mere casual (Galasso et al. 2018). It is furthermore locally naturalised in the Canary Islands (unpublished records by FV) and in Algeria in North Africa (Sakhraoui et al. 2023). It is also naturalised in parts of Australia (Randall 2007, Weeds of Australia 2023) and New Zealand (Schönberger et al. 2021). In some areas of its secondary range, A. maculata is considered to be an environmental weed.
Status in Portugal:—Naturalised. It was previously recorded in a list of “more or less naturalised” taxa (Almeida & Freitas 2006: 118), and later recorded as casual (Almeida 2012: 209) and as “Casual. Cultivated, escaped” (Silva et al. 2015: 75).
References:— Almeida & Freitas (2006); Almeida (2012); Güemes (2013); Silva et al. (2015).
Notes:— Aloe maculata has been recorded as naturalised in the Iberian Peninsula, in Spain and Portugal (Almeida & Freitas 2006: 119, Guillot Ortiz et al. 2008: 28–32, Almeida 2012: 209, Güemes 2013: 312). In places in Portugal the species has become naturalised through self-replacing populations and is now spreading without human aid. At some locations A. maculata has become invasive.
Aloe maculata is a distinctive species that can be easily identified based on the adaxial leaf surface that is spotted, often densely so, with whitish maculations (Fig. 2A–C) and its capitate inflorescences (Fig. 2D). Depending on the provenance of material of this species, flowering can take place at virtually any time of the year. Thus far only summer-flowering material of A. maculata has been observed in Portugal.
The only alooid material cultivated in Portugal with which A. maculata can be confused is A. × schimperi Todaro (1878: 70, plate 16) [A. maculata × A. striata Haworth (1804: 18)] (Fig. 3A–B), of which the arguably better known name A. × schoenlandii Baker (1902: 430), as ‘ Schönlandi ’, pro sp., is a synonym (Figueiredo & Smith 2016: 14). However, the leaf margins of A. × schimperi are distinctly pinkish—a character inherited from A. striata —and the flowers lack the prominent basal swellings evident in the flowers of A. maculata.
Aloe × commutata Todaro (1876: 75, t. 18) (Fig. 3C–D) (see Figueiredo & Smith 2012), of which the parents are A. grandidentata Salm-Dyck (1822: 3 [species no. 2]) and A. maculata, has a similar, typically ‘maculate aloe’-like vegetative morphological appearance as A. maculata. However, A. × commutata has elongated racemes (not capitate ones) and clavate (not basally inflated) flowers, and the leaf margins are concolorous, unlike those of A. × schimperi that are pinkish. Thus far we have not observed A. × commutata in cultivation anywhere in continental Portugal, although it is popular as a garden subject in some parts of the world, for example in the Boyce Thompson Arboretum, in Superior, Arizona, U.S.A. (see Smith 2005) and in the Huntington Botanical Gardens, in San Marino, California, U.S.A. (see Smith 1997), but, interestingly, not in South Africa, from where its parents originate.
In A. maculata, one other subspecies, A. maculata subsp. ficksburgensis (Reynolds 1937: 148) Gideon F.Sm. & Figueiredo in Smith et al. (2012b: 15), is recognised, which is only known from the eastern Free State, South Africa, and western Lesotho. This subspecies has not been observed in continental Portugal.
Notes
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Linked records
Additional details
Identifiers
Biodiversity
- Kingdom
- Plantae
- Phylum
- Tracheophyta
- Order
- Asparagales
- Family
- Asphodelaceae
- Genus
- Aloe
- Species
- maculata
- Taxon rank
- subSpecies
References
- Allioni, C. (1773 [?]) Auctarium ad synopsim methodicam stirpium horti reg. taurinensis. Melanges de Philosophie et de Mathematique de la Societe Royale de Turin pour les annees 1770 - 1773 5: 53 - 96. [Preprinted on 30 September 1773]. Available from: https: // www. biodiversitylibrary. org / item / 32648 # page / 85 / mode / 1 up (accessed 1 December 2023).
- Haworth, A. H. (1804) A new arrangement of the genus Aloe, with a chronological sketch of the progressive knowledge of that genus, and of other succulent genera. Transactions of the Linnean Society of London 7 (1): 1 - 28. https: // doi. org / 10.1111 / j. 1096 - 3642.1804. tb 00276. x
- Grace, O. M., Klopper, R. R., Figueiredo, E. & Smith, G. F. (2011) The aloe names book. Strelitzia 29. South African National Biodiversity Institute, Pretoria, and Royal Botanic Gardens, Kew, 232 pp. Available from: http: // hdl. handle. net / 20.500.12143 / 270 (accessed 1 December 2023).
- Almeida, J. D. de. (2012) Flora exotica subespontanea de Portugal continental (plantas vasculares). 5. a edicao. M. Sc. thesis. University of Coimbra, Coimbra, 281 pp. Available from: https: // docplayer. com. br / 48643620 - Flora-exotica-subespontanea-de-portugalcontinental-plantas-vasculares. html (accessed 1 December 2023).
- Almeida, J. D. de & Freitas, H. (2006) Exotic naturalized flora of continental Portugal. A reassessment. Botanica Complutensis 30: 117 - 130.
- Guemes, J. (2013) Aloe L. In: E. Rico, M. B. Crespo, A. Quintanar, A. Herrero & C. Aedo (Eds.) Flora iberica 20. Real Jardin Botanico, CSIC, Madrid, pp. 308 - 314. Available from: http: // www. floraiberica. es / floraiberica / texto / pdfs / 20 _ 183 _ 32 _ Aloe. pdf (accessed 1 December 2023).
- Silva, V., Figueiredo, E. & Smith, G. F. (2015) Alien succulents naturalised and cultivated on the central west coast of Portugal. Bradleya 33: 58 - 81. https: // doi. org / 10.25223 / brad. n 33.2015. a 10
- Tison, J. - M. & de Foucault, B. (2014) Xanthorrhoeaceae. Flora Gallica. Flore de France. Biotope Editions, Meze, pp. 299 - 301, whole work 1195 pp.
- Guillot Ortiz, D., Laguna Lumbreras, E. & Rossello Picornell, J. A. (2008) La familia Aloaceae en la flora aloctona valenciana. Bouteloua 6: 1 - 58. Available from: http: // www. floramontiberica. org / Bouteloua / MonogBouteloua _ 06 _ Aloaceae. pdf (accessed 1 December 2023).
- Aymerich, P. & Saez, L. (2019) Checklist of the vascular alien flora of Catalonia (northeastern Iberian Peninsula, Spain). Mediterranean Botany 40 (2): 215 - 242. https: // doi. org / 10.5209 / mbot. 63608
- Lamb, B. M. (1996) The genus Aloe (L.) in Gibraltar. Almoraima 15: 267 - 272.
- Mifsud, S. (2022) Malta wild plants. Available online at: https: // maltawildplants. com (accessed November 2022).
- Galasso, G., Conti, F., Peruzzi, L., Ardenghi, N. M. G., Banfi, E., Celesti-Grapow, L., Albano, A., Alessandrini, A., Bacchetta, G., Ballelli, S., Bandini Mazzanti, M., Barberis, G., Bernardo, L., Blasi, C., Bouvet, D., Bovio, M., Cecchi, L., Del Guacchio, E., Domina, G., Fascetti, S., Gallo, L., Gubellini, L., Guiggi, A., Iamonico, D., Iberite, M., Jimenez-Mejias, P., Lattanzi, E., Marchetti, D., Martinetto, E., Masin, R. R., Medagli, P., Passalacqua, N. G., Peccenini, S., Pennesi, R., Pierini, B., Podda, L., Poldini, L., Prosser, F., Raimondo, F. M., Roma-Marzio, F., Rosati, L., Santangelo, A., Scoppola, A., Scortegagna, S., Selvaggi, A., Selvi, F., Soldano, A., Stinca, A., Wagensommer, R. P., Wilhalm, T. & Bartolucci, F. (2018) An updated checklist of the vascular flora alien to Italy. Plant Biosystems 152 (3): 556 - 592. https: // doi. org / 10.1080 / 11263504.2018.1441197
- Sakhraoui, N., Verloove, F. & Smith, G. F. (2023) Aloe maculata All. (Asphodelaceae subfam. Alooideae): a new addition to the alien flora of Algeria and North Africa. Bradleya 41: 225 - 229. https: // doi. org / 10.25223 / brad. n 41.2023. a 16
- Randall, R. P. (2007 [September]) The introduced flora of Australia and its weed status. CRC for Australian Weed Management, Department of Agriculture and Food, Western Australia [Waite Campus, University of Adelaide, PMB 1, Glen Osmond, SA 5064 Australia.], 524 pp. Available from: https: // www. aabr. org. au / images / stories / resources / weeds / intro _ flora _ australia. pdf (accessed 1 December 2023).
- Weeds of Australia (2023) Aloe arborescens Mill. Available from: https: // keyserver. lucidcentral. org / weeds / data / media / Html / aloe _ arborescens. htm (accessed 31 January 2023).
- Schonberger, I., Wilton, A. D., Boardman, K. F., Breitwieser, I., De Lange, P. J., De Pauw, B., Ford, K. A., Gibb, E. S., Glenny, D. S., Greer, P. A., Heenan, P. B., Korver, M. A., Maule, H. G., Novis, P. M., Prebble, J. M., Smissen, R. D. & Tawiri, K. (2021) Checklist of the New Zealand Flora - Seed Plants. Manaaki Whenua-Landcare Research, Lincoln, 412 pp. https: // doi. org / 10.26065 / ax 7 t- 8 y 85
- Todaro, A. (1878 [1876 -]) Hortus Botanicus Panormitanus. Vol. 1. Cyri Visconti & Francisci Lao, Palermo, 64 pp. + XL plates.
- Baker, J. G. (1902) New or noteworthy plants. The Gardeners' Chronicle ser. 3, 32: 429 - 430. Available from: https: // www. biodiversitylibrary. org / item / 83820 # page / 494 / mode / 1 up (accessed 1 December 2023).
- Figueiredo, E. & Smith, G. F. (2016) Aloe × schimperi Tod. (Aloe maculata All. × Aloe striata Haw.), the earliest name applicable to the common and invasive nothospecies known as Aloe × schoenlandii Baker (Asphodelaceae: Alooideae). Haseltonia 22: 9 - 17. https: // doi. org / 10.2985 / 026.022.0103
- Figueiredo, E. & Smith, G. F. (2012) Clarifying the application of the long-confused name Aloe commutata, and the establishment of Aloe × commutata Tod. (Asphodelaceae). Bradleya 30: 25 - 32. https: // doi. org / 10.25223 / brad. n 30.2012. a 7
- Smith, G. F. (2005) The Boyce Thompson Arboretum near Superior, Arizona: a stunning botanical and succulent garden in cowboy country. Aloe 42 (1 & 2): 28 - 34.
- Smith, G. F. (1997) The Desert Garden of the Huntington Botanical Gardens: one of the great gardens of the world. Aloe 34 (3 & 4): 90 - 94.
- Reynolds, G. W. (1937) A new Aloe from South-West Africa, together with new varieties from the Transvaal and Orange Free State. Journal of South African Botany 3: 143 - 150.
- Smith, G. F., Figueiredo, E., Klopper, R. R. & Crouch, N. R. (2012 b) Aloe maculata All. (Asphodelaceae) in the Free State province, South Africa, and resurrection of ' var. ficksburgensis'. Bradleya 30: 13 - 18. https: // doi. org / 10.25223 / brad. n 30.2012. a 5