First record of Neea madeirana (Nyctaginaceae: Pisonieae) from the Peruvian Amazon

Primeiro registro de Neea madeirana (Nyctaginaceae: Pisonieae) da Amazônia peruana

ABSTRACT

Neea is one of the largest genera of Nyctaginaceae and comprises approximately 80 species distributed in the Neotropical region. Here, we report for the first time the occurrence of Neea madeirana in Peru, almost 50 years after it was first collected in this country, but was misidentified as Guapira noxia. We also insert N. madeirana in the identification key for Peruvian species of Neea and update the distribution map of N. madeirana. Given that we have not located any posterior specimen of G. noxia in Peruvian collections, and the original specimens cited as G. noxia correspond to N. madeirana, we suggest the exclusion of G. noxia from the Peruvian flora checklist.

KEYWORDS:
Caryophyllales; Loreto; new record; Pisonieae; taxonomy

RESUMO

Neea é um dos maiores gêneros de Nyctaginaceae e compreende aproximadamente 80 espécies distribuídas na região neotropical. Aqui, relatamos, pela primeira vez, a ocorrência de Neea madeirana no Peru, quase 50 anos depois de ter sido coletada pela primeira vez neste país, mas foi erroneamente identificada como Guapira noxia. Também inserimos N. madeirana na chave de identificação para espécies peruanas de Neea e atualizamos o mapa de distribuição de N. madeirana. Dado que não localizamos nenhum espécime posterior de G. noxia nas coleções peruanas, e os espécimes originais citados como G. noxia correspondem a N. madeirana, sugerimos a exclusão de G. noxia da flora peruana.

PALAVRAS-CHAVE:
Caryophyllales; Loreto; novo registro; Pisonieae; taxonomia

Neea Ruiz & Pav. is one of the largest genera in the family Nyctaginaceae, comprising approximately 80 species distributed in the Neotropical region (Furlan and Giulietti 2014), and is most diverse in the Amazonas and Orinoco river basins and the Guayana Shield region (Steyermark and Aymard 2003; Costa et al. 2021). The genus is found in eleven neotropical countries, of which Brazil (ca. 23 spp.), Venezuela (ca. 25), and Peru (ca. 20) (Grandtner and Chevrette 2014) have the most species.

In the Peruvian Amazon, Neea is represented by 13 species that occur in different habitats, such as tropical lowland and montane forests (Vásquez et al. 2018). In the state of Loreto, there are records of eight species that occur in upland primary forests (Vásquez 1997; Vásquez et al. 2018). However, cataloguing the diversity of Neea is still a work in progress, and many specimens in collections remain potentially unidentified or misidentified (Costa et al. 2023). While reviewing the Herbario Amazonense (AMAZ) collection, we found specimens identified as Guapira noxia (Netto) Lundell collected in Loreto, Peru. However, G. noxia is typical of the Cerrado savanna in Brazil. Therefore, we reexamined these specimens and redescribe them here as Neea madeirana Standl., which is herewith reported for the first time for Peru.

We analyzed specimens at herbaria AMAZ and HH, and online images of specimens at F, MO and U (acronyms follow Thiers 2022), all misidentified as G. noxia. In addition, between July and November 2020, we conducted expeditions in the Napo River basin in the Peruvian Amazon. The material from Peru was morphologically compared with the N. madeirana holotype and its respective synonyms, according to Furlan and Giulietti (2014) (Neea krukovii Standl. and Neea aeruginosa Standl.), available at BM, F, K, NY, and RB. The material was measured using a digital caliper, following the terminology of Radford et al. (1974), Furlan and Giulietti (2014), and Ellis et al. (2009) for leaf architecture. The description of Neea huachamacarae Steyerm., followed Steyermark and Aymard (2003).

Quantitative morphological characters were presented as mean, standard deviation and the range (maximum and minimum), according to Vasconcelos et al. (2020). To prepare an updated distribution map for N. madeirana, geographical coordinates of records throughout its distribution range were obtained from herbarium specimen labels available online on SpeciesLink (2021) and Reflora (2021). The map was made with the package Maps (Becker and Wilks 2013) in the program R (R Core Team 2020). We determined the conservation status of the species using IUCN criteria (IUCN 2021) with the ConR package (Dauby et al. 2017) estimating the area of occupancy (AOO), extent of occurrence (EOO), and number of subpopulations.

Neea madeirana Standl.

(Figures 1 and 2)

Figure 1
Neea madeirana. A - fertile branch; B - detail of veins on abaxial surface; C-D - pistillate flower; E-F - staminate flower; G - infructescence; H - detail of infructescence axis; I - anthocarp; J; - cupule of anthocarp. (A-B, G-J from R. Soplin 37-A-5; C-D from N. T. Silva 5401) Credit: Francisco Farroñay.

Figure 2
Updated distribution map of Neea madeirana.

Description - Trees, 10-30 m tall. Trunk 25 cm DBH. Leaves subopposite; petioles 1.3-(2.3 ± 0.9)-4.9 cm long, tomentose; blades 5.4-(14 ± 5.7)-23.6 × 3.2-(7.2 ± 3)-13.4 cm, elliptic or ovate, surface smooth, adaxially and abaxially pubescent to tomentose, trichomes reddish; apex attenuate or acute; base acute or asymmetric; margin entire. Midrib pinnate, adaxially impressed or prominent, abaxially prominent; secondary venation brochidodromous, with 6-(10.2 ± 2.7)-15 pairs, adaxially impressed, abaxially prominent, tertiary veins alternate percurrent. Inflorescences 1-3, 1.6-(3.1 ± 1.3)-3.9 cm long, in terminal to cauliflorous cymes, with dense trichomes, tomentose or ferruginous-puberulous, reddish; primary branches 1.4-(2.4 ± 0.8)-3.4 cm long, opposite to alternate, branched into 3-5 secondary axes, these subopposite, with dense reddish trichomes and groups of flowers congested at the apical portion. Bracts not observed. Bracteoles deltoid, with reddish trichomes covering the surface. Staminate buds not observed. Staminate flowers 4-(5.4 ± 0.6)-6.5 × 2-(2.4 ± 0.2)- 2.5 mm, urceolate, 5-lobed, lobes close, deltoid, densely pubescent. Pistillate flowers 2.2-(2.6 ± 0.2)-2.5 × 1.5-(1.5 ± 0.1)-1.7 mm, tubular, 5-lobed, lobes close, deltoid, densely pubescent; ovary 0.7-(0.9 ± 0.2)-1 mm long, elliptic to ovoid; style 0.7-(0.9 ± 0.3)-1.4 mm long; stigma entire; staminodes 4‒6, ca. 1-(1.3 ± 0.2)-1.5 mm long. Infructescences 7.3-(8.6 ± 0.9)-9.3 cm long, puberulent. Anthocarps 1.5-(1.8 ± 0.3)-2.2 cm, elliptic; apical cupule apiculate or commonly absent.

Material examined - PERU. Loreto: Maynas: Santa María de Nanay, Río Nanay, halfway between Santa María de Nanay and Iquitos, 3°50’S, 73°30’W, c.a. 140 m, 23 February 1981 (fr.), A.H. Gentry et al. 31563 (AMAZ![12787], F!, MO!, U!); ibid: Santa María de Nanay, 3°52’52.00”S, 73°29’31.00”O, c.a. 90m, 1 October 1981 (bud), J.J. Pipoly et al. 12666 (MO![738340]); Requena: Jenaro Herrera, km 2.8 de la carretera Jenaro Herrera-Angamos, arboreto de terraza alta del CIJH, 04°50’S, 73°45’W, 10 January 1983 (fl.), D. Angulo 7/153 (HH![2603]); Maynas: Puerto Almendras: Río Nanay, 03°45’S, 73°25’W, 122m, 25 October 1984 (fl.), R. Vásquez et al. 5849 (AMAZ![21143], MO!); Requena: Jenaro Herrera, 04°50’S, 73°45’W, 122m, 13 September 1987 (fl.), R. Vásquez et al. 9538 (AMAZ![113], MO!); Río Apayacu, Terra firme forest on low rolling hills in the upper watershed of the Apayacu River. Soils well-drained 38% sand and 16% clay, 3° 07›00»S, 72°42›45»W, 16-23 August 2003 (sterile), N. Pitman et al. 9744 (AMAZ![34404]); Santa Clotilde, Río Napo, bosque sobre arcilla, 1° 0’18.19”S 74°49’7.08”O, c.a. 160 m, 22 November 2020 (fr.), R. Soplin et al. 37-A-5 (AMAZ![97584]). BOLIVIA. Pando: W bank of rio Madeira, 2 km above Abunã, 10°24’57.36”S 65°29’14.87”O, 25 July 1968 (fr.), G.T. Prance et al. 6492 (INPA!, NY). BRAZIL. Acre: Mâncio Lima: Ramal do Banho a 5 Km da Sede do Município, 7°54’0.00”S, 73°28’12.00”O, 8 November 1991 (fr.), C.A. Cid Ferreira et al. 10629 (INPA!,NY, UFAC!); Amazonas: Manaus: Reserva Florestal Adolfo Ducke, 2°52’48.00”S, 59°58’12.00”O, 8 October 2015 (sterile), G.P. Viana s.n (INPA!, FUEL!); ibid: 2°52’48.00”S, 59°58’12.00”O, 31 Octuber 1994 (buds), A. Vicentini & C.F, Silva 754 (IAN!; FUEL!; NY!); Presidente Figueiredo: Rebio Uatumã, grade do PPBio, 0°59’60.00”S 59° 0’0.00”O, 25 September 2007 (fl.), J.G de Carvalho-Sobrinho 1683 (INPA!, FUEL!); São Gabriel da Cachoeira: Camanaús, Alto Rio Negro, abaixo de Camanaus. Caatinga com piassabal, 0° 7’12.00”S, 67°34’48.00”O, 15 October 1932 (bud), W.A. Ducke 25641 (RB); Pará: Almeirim: Área Cova da Onça, 2°18’55.33”S, 59°41’7.70”O, 15 August 1979 (fl.), N.T. Silva 5401 (INPA!); Rondônia: Manicoré: RADAM/ BRASIL SB-20-XD, Sub-base do Projeto RADAM/BRASIL SB-20-XD-Pto.02, 5°49’60.00”S 61°16’60.00”O, 19 August 1976 (fl.), C.D.A. Mota s.n (INPA!); Mato Grosso: Reserva Cirecatinga, Próximo Alcaititu - Reserva Ciracatinga Sopezal, 12°41’60.00”S 58° 5’60.00”O, 24 August 1995 (fl.), R. Godinho 2 (INPA!)

Distribution and habitat - It is known to occur in terra firme forests in Brazil, in the states of Amapá, Amazonas, Mato Grosso, Maranhão, Pará, and Rondônia (Furlan and Giulietti 2014; Costa et al. 2020), and in Bolivia, in the state of Pando. Here we expand the known distribution to Peru, Loreto state, where it occurs in upland primary forests with well-drained, sandy and clayey soils (Figure 2).

Conservation status - Based on the updated distribution (Brazil, Bolivia, and Peru), EOO is 4,478,116 km² and AOO is 144 km², with 38 subpopulations (radius 5 km). According to IUCN criteria, Neea madeirana is categorized as of Least Concern (LC).

Diagnosis - Neea madeirana is characterized by Furlan and Giulietti (2014) by the reddish trichomes covering the midrib on both leaf surfaces (Figure 1a,b) and reproductive structures (e.g., inflorescence, bracts, bracteoles, and flowers) (Figure 1a-h), inflorescence and infructescence with opposite, alternate or subvercillate primary axes (Figure 1a-g), urceolate, tomentose staminate flowers with long, truncated lobes (Figure 1e,f), and tubular, tomentose pistillate flowers with long, linear lobes (Figure 1c,d). Relative to the diagnosis by Furlan and Giulietti (2014) for Neea madeirana from Brazil, the most relevant differences we observed to the specimens from Peru were that the indument of the staminate perianth is densely pubescent (vs. puberulous or glabrescent) and the cupule of the anthocarps are apiculate (vs. immerse) (see Figure 1).

The misidentification of Neea madeirana as Guapira noxia was probably due to the vegetative similarity between them, as both have leaves with a tomentose adaxial surface with reddish trichomes. However, N. madeirana can be differentiated from G. noxia by the shape of the tertiary veins (alternate-percurrent vs. ramified), the shape of the staminate flowers (urceolate vs. campanulate), the position of the stamens in the perianth (included vs. exserted), and the shape of the pistillate flower lobes (deltoid vs. papillated) (see Furlan and Giulietti 2014). Also, G. noxia in Brazil has a greater affinity for savanna environments, while N. madeirana occurs predominantly in Amazonian rainforests (terra firme forests and dry forests on slopes) (see Furlan and Giulietti 2014).

We recommend removing G. noxia from the Peruvian flora list, as the specimens cited in the Peruvian tree checklist by Vásquez et al. (2018) (collection Gentry 31563) are Neea madeirana as reported in this study.

Updated key to the species of Neea in Peru (modified from Costa et al. 2020 )

1. Leaves alternate ....................... N. virens Poepp. ex Heimerl

1. Leaves opposite, subopposite, or verticillate ...................... 2

2. Leaves equal or more than 30 cm long ............................. 3

3. Peduncle flexible, less than 3 cm thick .................................................................................. N. laxa Poepp. & Endl.

3. Peduncle inflexible, more than 3 cm thick ...................... 4

4. Bracts deltoid, ca. 1.5 mm long ................................................................................. N. floribunda Poepp. & Endl.

4. Bracts linear or lanceolate, more than 2 mm long ......... 5

5. Pistillate flowers glabrous .................................................................................................... N. mapirensis Standl.

5. Pistillate flowers pubescent ... N. verticillata Ruiz & Pav.

2. Leaves less than 30 cm long .............................................. 6

6. Intersecondary veins less than 1 cm from major secondary veins ............................ N. ovalifolia Spruce ex. J.A. Schmidt

6. Intersecondary veins more than 1 cm from major secondary veins .................................................................. 7

7. Leaves pubescent .......................................................... 8

8. Intercostal tertiary veins ramified ............................................................................... N. parviflora Poepp. & Endl.

8. Intercostal tertiary veins opposite percurrent ........................................................................... N. madeirana Standl.

7. Leaves glabrous ............................................................ 9

9. Staminate flowers tubular, with minute trichomes at the base ....................................... N. oppositifolia Ruiz & Pav.

9. Staminate flowers subpandurate-tubular or cylindric-campanulate, glabrous .................................................. 10

10. Staminate flowers 4-5.5 mm long ...................................................................... N. macrophylla Poepp. & Endl.

10. Staminate flowers 7.5-8 mm long ............................................................................ N. huachamacarae Steyerm.

ACKNOWLEDGMENTS

We thank the staff of the Herbarium Amazonense (AMAZ) and Herbario Herrerense (HH) at Universidad Nacional de la Amazonía Peruana (UNAP) and the Instituto de Investigaciones de la Amazonía Peruana (IIAP), respectively, for allowing us access to their collection. We also thank the Servicio Nacional Forestal y de Fauna Silvestre (SERFOR-Peru) for the logistical and financial support to carry out fieldwork.

REFERENCES

• Becker, R.A.; Wilks, A.R. 2013. Maps in S. AT&T Bell Laboratories Statistics Research Report (93.2). ( (http://ect.bell labs.com/sl/doc/93.2.ps ). Accessed on 25 Jul 2021.
  » http://ect.bell labs.com/sl/doc/93.2.ps
• Costa, D.S.; Rossetto, E.F.S.; Sá, C.F.C. 2020. Neea in Flora e Funga do Brasil. Jardim Botânico do Rio de Janeiro. ( (https://floradobrasil. jbrj.gov.br/FB24043 ) . Accessed on 24 Oct 2022.
  » https://floradobrasil. jbrj.gov.br/FB24043
• Costa, D.; Rossetto, E.F.S.; Terra-Araujo, M.H. 2021. Neea campanulata (Nyctaginaceae: Pisonieae), a new species from humid forests, Pará State, Brazil. Kew Bulletin, 76: 625-631.
• Costa, D.; Sandoli Rossetto, E.F.; Terra Araujo, M.H.. 2023. A new species of Neea (Pisonieae, Nyctaginaceae) from central and eastern Amazonia, Brazil, with a note on the typification of Neea ovalifolia Brittonia 75: 307-317.
• Dauby, G.; Stévart, T.; Droissart, V.; Coisaux, A.; Deblauwe, V.; Simo-Droissart, M.; et al. 2017. ConR: An R package to assist large-scale multispecies preliminary conservation assessments using distribution data. Ecology and Evolution, 7: 11292-11303.
• Ellis, B.; Daly, D.C.; Hickey, L.J.; Johnson, K.R.; Mitchell, J.D.; Wilf, P.; Wing, S.L. 2009. Manual of Leaf Architecture Cornell University Press, New York, 200p.
• Furlan, A; Giulietti, A.M. 2014. A tribo Pisonieae Meisner (Nyctaginaceae) no Brasil. Boletim De Botânica, 32: 145-268.
• Grandtner, M.M.; Chevrette, J. 2014. Dictionary of Trees, Volume 2: South America: Nomenclature, Taxonomy and Ecology Laval University, Quebec, 1172p.
• IUCN. 2021. The IUCN Red List of Threatened Species. Version 2021-1. ( (https://www.iucnredlist.org ). Accessed on 25 July 2021.
  » https://www.iucnredlist.org
• Radford, A.E.; Dickison, W.C.; Massey, J.R.; Bell, C.R. 1974. Vascular Plant Systematics. Harper & Row Publishers, New York, 891p.
• R Core Team 2020. R: A language and environment for statistical computing. Vienna, Austria. ( (https://www.r-project.org/ ). Accessed on 25 Jul 2021.
  » https://www.r-project.org/
• Reflora. 2021. Reflora Virtual Herbarium. ( (http://reflora.jbrj.gov.br/reflora/herbarioVirtual/ ). Accessed on 25 July 2021.
  » http://reflora.jbrj.gov.br/reflora/herbarioVirtual/
• SpeciesLink. 2021. Centro de Referência em informação Ambiental. ( (http://www.splink.org.br/index?lang=pt ). Accessed on 25 July 2021.
  » http://www.splink.org.br/index?lang=pt
• Steyermark, J.A.; Aymard, G.A. 2003. Nyctaginaceae In: Berry, P.C.; Yatskievych, K.; Holst, B.K. (Eds.). Flora of the Venezuelan Guayana v.7. Missouri Botanical Gardens Press, St. Louis, p.101-118p.
• Thiers, B. 2022. [continuously updated]. Index Herbariorum. A global directory of public herbaria and associated staff. New York Botanical Garden’s Virtual Herbarium. ( (http://sweetgum.nybg.org/science/ih/ ). Accessed on 20 Jul 2023.
  » http://sweetgum.nybg.org/science/ih/
• Vásquez, R. 1997. Flórula de las Reservas Biológicas de Iquitos, Perú: Allpahuayo-Mishana, Explornapo Camp, Explorama Lodge Monographs in Systematic Botany from the Missouri Botanical Garden. St. Louis, 1046p.
• Vásquez, R.; Rojas, R.; Monteagudo, A.; Valenzuela, L.; Huamantupa, I. 2018. Catálogo de los árboles del Perú. Revista Q’euña, 9: 1-167.
• Vasconcelos, C.C.; Adrianzén, M.U.; Camargo, J.L.C.; Terra-Araujo, M.H. 2020. Pouteria kossmanniae (Sapotaceae): a new species from Central Amazonia, Brazil. Phytotaxa 447: 265-275.

• CITE AS:

  Costa, D.S.; Farroñay, F.; Dávila-Doza, H.P.; Villacorta-Mora, L. 2024. First record of Neea madeirana (Nyctaginaceae: Pisonieae) from the Peruvian Amazon. Acta Amazonica 54: e54bc23155

Data availability

The data that support the findings of this study are not publicly available.

Edited by

ASSOCIATE EDITOR:

Natalia Ivanauskas

Publication Dates

• Publication in this collection
  08 Jan 2024
• Date of issue
  Jan-Mar 2024

History

• Received
  09 June 2023
• Accepted
  27 Oct 2023