Research Article |
Corresponding author: Rosa Cerros-Tlatilpa ( tlatilpa@uaem.mx ) Academic editor: Luiza Teixeira-Costa
© 2025 María Guadalupe Maldonado-Borja, Rosa Cerros-Tlatilpa.
This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Citation:
Maldonado-Borja MG, Cerros-Tlatilpa R (2025) A new and endemic species of Struthanthus (Loranthaceae) from Guerrero, Mexico. Plant Ecology and Evolution 158(2): 195-204. https://doi.org/10.5091/plecevo.145707
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Background and aims – Struthanthus is a neotropical genus with 60 to 70 species, distributed from northern Mexico to Argentina. Eighteen species are reported in Mexico. During fieldwork to investigate Struthanthus in Mexico, a new species was collected in the state of Guerrero. We present a full description, distribution map, illustrations, and photographs of an unusual new Struthanthus species endemic to Guerrero, Mexico.
Material and methods – This study is based on fieldwork, literature revision, and examination of herbarium material. Collected specimens were prepared for storage in the herbarium, analysed, measured, described, and photographed. Preliminary conservation assessment is based on spatial analyses following IUCN guidelines and criteria.
Key results – We propose a new species of Struthanthus for Guerrero, Mexico, S. longipetiolatus. This species is only known from cloud forests, oak-pine forests, and oak forests in the province of Sierra Madre del Sur, in the state of Guerrero. A distribution map and an identification key are provided for S. longipetiolatus and its morphologically similar congeners in the region.
Conclusion – The newly described species increases the number of Struthanthus species in Mexico to 19 and the number of endemic species to nine. This discovery underlines the need for continued botanical inventories and research on parasitic plants.
endemism, hemiparasite, mistletoe, taxonomy
Struthanthus Mart. is a complex genus of Loranthaceae because it shares morphological characters with other genera of small flowers, such as Cladocolea Tiegh. (
The description is based on our collections from Sierra Madre del Sur (SMS) in Guerrero and herbarium specimens from ENCB, HUMO, MEXU, and XAL (acronyms follow
MEXICO – Guerrero • Leonardo Bravo, Los Morros; 17°41’27.06”N, 99°48’8.93”W; 2098 m; 22 Apr. 2023; ♂ fl.; Maldonado-Borja 87; holotype: HUMO [40027].
Morphological comparison of Struthanthus longipetiolatus with S. ibe-dzi, S. racemosus, and S. ramiro-cruzii.
Characters | S. ibe-dzi | S. longipetiolatus | S. racemosus | S. ramiro-cruzii |
Stem nodes | compressed and bicarinate | subterete to complanate | terete | terete |
Leaf shape | ovate to lanceolate, rare elliptical | lanceolate, ovate, or narrowly ovate | narrowly lanceolate to subulate-falcate | ovate to lanceolate, cordate when mature |
Leaf apex shape | acute to acuminate | long acuminate to acute mucronate | apiculate | apiculate or acute |
Leaf base shape | cuneate to oblique | attenuate to oblique | attenuate to cuneate | subcordate to truncate |
Petiole length (cm) | 0.25–1.2 | 1.2–3.2 | 0.6–0.9 | 0.5–1 |
Inflorescences per axil | 1 | 1 | 1 | 1(2) |
Inflorescence subunit | mostly triads, rarely monads in the apical flowers of inflorescence | triads | monads | triads, rarely monads or dyads in the apical flowers of the inflorescence |
Flowers in triads (monads if applicable) | central sessile and laterals pedicellate | central sessile and laterals pedicellate | monads pedicellate | central sessile and laterals pedicellate |
Pistillate inflorescence length (cm) | 2–5 | 3.5–7.6 | 3–4.5 | 2.5–6.2(–10.5) |
Triads/monads number per pistillate inflorescence | 6–12(–15) triads | 10–14(–16) triads | 8–10(–12) monads | 8–20 triads |
Pistillate flower length from base of ovary (mm) | 5.8–7.2 | 4.7–6 | 3.8–5 | 5–5.8 |
Staminate inflorescence length (cm) | 2–6.8 | 3.6–10.8(–12) | 3.6–4.6 | 2.5–8 |
Triads/monads number per staminate inflorescence | 6–16(–19) | 12–16(–18) | 10–12 monads | 10–16 |
Staminate flower length from base of ovary (mm) | 6–9 | 6.2–10.2 | 4.6–6 | 6–7 |
Flower colour | green | olive green yellowish to pink-reddish | reddish | greenish-yellow |
Struthanthus longipetiolatus is similar to S. ibe-dzi, S. racemosus, and S. ramiro-cruzii. Plants scandent and pendant with inflorescences in racemes and triads peduncled, the central flower sessile, and the lateral ones pedicellate as in S. ibe-dzi and S. ramiro-cruzii. However, the new taxon is distinguished by its olive green yellowish to pink-reddish stems, petioles, leaves, inflorescence, petals, and style of the pistillate flower and by the long petioles reaching up to 3.2 cm.
Struthanthus longipetiolatus. A. Habit, scandent and pendant shrub. B. Staminate inflorescence. C. Lateral view of a staminate flower with two petals removed to show the anthers. C1. Front and side view of anther basifixed, dimorphic, and elliptical with an apicular connective. C2. Dissected staminate flower with two alternating stamens, stylodium straight to slightly wavy, and undifferentiated stigma. D. Lateral view of a pistillate flower with two petals removed to show the contour of the convolute style. D1. Dissected pistillate flower with staminodes, a convolute style, and a capitate stigma. E. Mature leaf. F. Infructescence. Male inflorescence from Maldonado-Borja 87 (A, B, C, C1, C2); female inflorescence from Maldonado-Borja 119 (D, E) and Maldonado-Borja 54 (F). Illustration by Eduardo Santaella.
Shrubs woody, scandent, pendant, 0.8–4(–6.5) m long, perennial, hemiparasitic, dioecious. Haustorium terete, with several epicortical roots at the base of the plant; epicortical roots produce secondary haustoria that attach to the host. Stems 1–4.5 mm diameter, voluble, terete to subterete, glabrous, olive green to pinkish, and brown greenish when dried, with lenticels when mature; with epicortical roots. Nodes subterete to complanate, bicarinate mainly when young; stem internodes 3.5–8.6(–10) cm long. Leaves opposite to subopposite; petioles 1.2–3.2 cm long, channelled near the leaf blade base, resupinate; blades lanceolate, ovate, or narrowly ovate, 1.2–5.0 × 6.5–16.5 cm, apex long acuminate to acute mucronate, base attenuate to oblique, olive green to pinkish-reddish, margin entire, repand when mature, hyaline, venation pinnate, glabrous, papyraceous. Inflorescences indeterminate, axillary, 1 per axil, racemes of triads, rarely paniculated; rachis subterete to applanate, nodes plane, triads opposite to subopposite, decussate; central flower from triad sessile, lateral flowers pedicellate 0.22–0.65 mm long. Bracts and bracteoles caducous, cupuliform. Pistillate inflorescences 3.5–7.6 cm long, peduncles 0.5–1.35 cm long, 10–14(–16) triads, triad peduncle 0.5–1.28 mm long. Staminate inflorescences 3.6–10.8(–12) cm long, peduncle 0.45–1.6(–2) cm long, 12–16(–18) trads, triad peduncle 0.6–1 mm long. Pistillate flowers hexamerous. Flower buds cylindrical, rounded at the apex; mature flowers 1.25–2.2 × 4.7–6 mm, calyculus irregular, 0.1–0.2 mm, petals linear 0.5–0.75 × 2.8–3.65 mm, olive green yellowish to pink-reddish, staminodes one series; nectary globose, hexagonal, surrounding the style; ovary inferior 1–1.2 × 2–2.6 mm, green yellowish; style strongly convolute, 3.2–4 mm long, stigma capitate, pink-reddish when ripe. Staminate flowers hexamerous, central flower of triad sessile, pedicels of lateral flowers 1.2–2.2 mm long. Flower buds claviform with rounded apex; mature flowers 2.4–4.8 × 6.2–10.2 mm, petals linear, 0.8–1.25 × 5–8.5 mm, olive green yellowish to pink-reddish, without trichomes at the insertion of the petal and the filament; anthers basifixed, dimorphic, and elliptical, 0.9–1.18 × 2.2–3.2 mm, fully attached to petals, asymmetrical theca, apicular connective; calyculus irregular, green yellowish 0.2–0.5 mm, vestigial ovary 1.2–2.25 × 1–2 mm, nectary globose, hexagonal, surrounding the stylodium base; stylodium straight to slightly wavy, 1.4–3 mm long, stigma undifferentiated. Fruit a berry, ovoid, green when immature, orange to vermillion when ripe, bluish-black when dry, glaucous, 3.45–6.65 × 8.2–10 mm. Seed ovoid, 2.2–4.8 × 4.2–5.2 mm.
Struthanthus longipetiolatus. A. Pistillate inflorescence with reddish styles. B. Dissected pistillate flower with staminodes (st), a convolute style, and a capitate stigma (s) above the ovary (o). C. Hexamerous nectary (ne), irregular calyculus (ca). D. Staminate inflorescence with pendant petioles (p), pink-reddish leaves. E. Dissected staminate flower showing two series of stamens (S1, S2), basifixed, dimorphic, with elliptical anthers and apicular connective; stylodium slightly wavy, and undifferentiated stigma. F. Hexamerous nectary (ne), irregular calyculus (ca). G. Sexual dimorphism, female (left) and male (right) flowers, two petals were removed. H. Immature fruits. I. Mature orange and vermillion fruits. Photos by Rosa Cerros-Tlatilpa (A, D, H, I) and Maria Guadalupe Maldonado-Borja (B, C, E, F, G).
Struthanthus longipetiolatus is endemic to Guerrero, Mexico, in cloud forests, oak-pine forests, and oak forests in the Sierra Madre del Sur Biogeographic Province (
Struthanthus longipetiolatus mainly parasitizes Pinus spp. (Pinaceae), but also Ostrya virginiana (Mill.) K.Koch (Betulaceae), and Quercus spp. (Fagaceae). It was also found parasitizing cultivated fruit trees such as Crataegus mexicana Moc. & Sessé ex DC., Prunus persica (L.) Batsch (Rosaceae), and Psidium guajava L. (Myrtaceae) (Fig.
Flowering from May to August and fruiting from December to February.
The specific epithet refers to the characteristic long petioles in this taxon, unique among Mexican species.
Endangered: EN B1ab(iii) + 2ab(iii). Struthanthus longipetiolatus is known only from the centre region of Guerrero in the Province of Sierra Madre del Sur. The extent of occurrence (EOO) is estimated at 293 km2 (criterion B1: EN) and the area of occupancy (AOO) is estimated at 52 km2 (criterion B2: EN). There are four locations (condition a) and there is a continuing decline in habitat quality (condition b(iii)), together indicating Endangered under criteria B1 and B2. The state of Guerrero experiences an annual deforestation rate averaging 13,311.8 hectares/year (
MEXICO – Guerrero • Chilpancingo de los Bravos, Llanos de Tepoxtepec; 17°28’36.13”N, 99°31’36.35”W; 2331 m; 12 Jan. 2022; fr.; Maldonado-Borja 49; HUMO • ibid.; 12 Jan. 2022; fr.; Maldonado-Borja 50; HUMO • ibid.; 12 Jan. 2022; fr.; Maldonado-Borja 51; HUMO • ibid.; 18 Apr. 2022; fr.; Maldonado-Borja 54; HUMO • ibid.; 18 Apr. 2022; ♂ fl.; Maldonado-Borja 55; HUMO • ibid.; 13 May 2022; ♀ fl.; Maldonado-Borja 71; HUMO • ibid.; 26 Aug. 2023; ♂ fl.; Maldonado-Borja 80; HUMO • Km 7 hacia llanos de Tepoxtepec; 17°28’44.11”N, 99°31’9.44”W; 2218 m; 18 Apr. 2022; ♀ fl.; Maldonado-Borja 53; HUMO • Llanos de Tepoxtepec; 17°28’42.99”N, 99°31’31.51”W; 2269 m; 18 Apr. 2022; ♂ fl.; Maldonado-Borja 56; HUMO • Camino hacia el parque de Llanos de Tepoxtepec; 17°27’48.3”N, 99°32’49.6”W; 2577 m; 13 May 2022; ♀ fl.; Maldonado-Borja 68; HUMO • Camino hacia el parque de Llanos de Tepoxtepec; 17°28’33.8”N, 99°31’50.4”W; 2399 m; 13 May 2022; ♂ fl.; Maldonado-Borja 69; HUMO • ibid.; 13 May 2022; ♂ fl.; Maldonado-Borja 70; HUMO • ibid.; 26 Aug. 2022; ♀ fl.; Maldonado-Borja 78; HUMO • Camino hacia el parque de Llanos de Tepoxtepec; 17°28’32.79”N, 99°31’48.59”W; 2376 m; 26 Aug. 2022; ♀ fl.; Maldonado-Borja 79; HUMO • Llanos de Tepoxtepec; en bifurcación camino al Parque, a lado de Huerta de duraznos; 17°28’37.07”N, 99°31’26.32”W; 2383 m; 17 Jun. 2023; ♀ fl.; Maldonado-Borja 117; HUMO • ibid.; 17 Jun. 2023; ♂ fl.; Maldonado-Borja 118; HUMO • ibid.; 17 Jun. 2023; ♀ fl., fr.; Maldonado-Borja 119; HUMO • Llanos de Tepoxtepec, km 8 a 200 m de la telesecundaria; 17°28’33.77”N, 99°31’50.29”W; 2265 m; 26 Aug. 2022; ♂ fl.; Maldonado-Borja 120; HUMO • ibid.; 26 Aug. 2022; ♀ fl.; Maldonado-Borja 121; HUMO • General Heliodoro Castillo, Carretera de Puerto del Varal a Verde Rico; 17°42’32.75”N, 99°54’44.44”W; 2222 m; 24 Apr. 2023; ♂ fl.; Maldonado-Borja 96; HUMO • Leonardo Bravo, Filo de Caballos, Chichihualco; [17.64897°N, -99.82453°W]; 2240 m; 3 Jun. 1983; ♂ fl.; Martínez S. 3895; MEXU, ENCB • ½ km al E de Tres Caminos, Chichihualco; [17.71117°N, -99.77511°W]; 2420 m; 4 May 1987; ♀ fl.; Lorea 4083; XAL • Comunidad “Campo de Aviación”; 17°39’9.51”N, 99°49’24.89”W; 2200 m; 22 Apr. 2023; ♂ fl.; Maldonado-Borja 88; HUMO.
A single individual can parasitize different tree strata, forming the main haustorium on the top branches and descending to the lower branches, measuring up to 6.5 m in length. This new species is characterized by its long petioles up to 3.2 cm. It can also have olive green yellowish to pink-reddish tones in stems, leaves, flower peduncles, petals, and even in the styles. Unlike other species of the genus, S. longipetiolatus has a well-marked sexual dimorphism, the staminate flowers being larger compared to the pistillate flowers (Fig.
1. | Stems with exfoliating bark; condensed inflorescence | S. condensatus |
– | Stems without exfoliating bark; non-condensed inflorescence | 2 |
2. | Inflorescence spike-like, 1–5 per axil; pedicel on the fruit conspicuously accrescent, pendant | S. quercicola |
– | Inflorescence racemiform,1–2 per axil; pedicel on the fruit slightly thickened, straight | 3 |
3. | Triads subsessile; triad flowers all sessile | 4 |
– | Triads pedunculate; lateral flowers pedicellate and central flower sessile | 5 |
4. | Leaves with petioles 0.8–1.2 cm; unisexual flowers; non-accrescent pedicels on the fruit; fruit without glands, reddish | S. interruptus |
– | Leaves sessile to subsessile, petioles 0.4–0.6 cm; bisexual flowers; accrescent pedicels on the fruit; fruit with glands, brown-reddish | S. venetus |
5. | Leaves ovate to lanceolate, cordate when mature, apex apiculate or acute, base subcordate to truncate | S. ramiro-cruzii |
– | Leaves lanceolate, ovate or narrowly ovate, apex acute to long acuminate to apiculate, base acute to attenuate | 6 |
6. | Petiole 0.6–0.9 cm long, subunit of inflorescence in monads | S. racemosus |
– | Petiole 1.25‒3.2 cm long, subunit of inflorescence in triads | S. longipetiolatus |
Struthanthus longipetiolatus morphologically resembles S. ibe-dzi, S. racemosus, and S. ramiro-cruzii because the four species have inflorescences in racemes. Additionally, unlike other Struthanthus species, they have stamens fully attached to the petal and lack trichomes at the base of the petal’s insertion with the filament. The four species are distributed in the Sierra Madre del Sur, with S. ibe-dzi being endemic to the state of Oaxaca. In contrast, S. longipetiolatus, S. racemosus, and S. ramiro-cruzii are found in the state of Guerrero. Like S. ramiro-cruzii and S. ibe-dzi, S. longipetiolatus has triads with pedicellate lateral flowers and a sessile central one. Struthanthus racemosus differs from S. longipetiolatus in having monads instead of triads in addition to petioles 0.60–0.90 mm long. Additionally, S. longipetiolatus and S. ramiro-cruzii are found in the same locality, but they differ mainly in the leaf shape and pedicel length. Moreover, S. ramiro-cruzii has leaves ovate to lanceolate, cordate when mature, with a petiole 0.5–1.0 cm long while S. longipetiolatus has leaves lanceolate, rarely ovate with apex acute to long acuminate, mucronate, and a base acute to obtuse with a slender petiole up to 3.20 cm long. Another notable difference is the stem colour, which ranges from olive green to pink-reddish, and extends to leaves, flowers peduncles, petals, and even the styles. Plant pigments are involved in various functions including photosynthesis, for example, flowers from calyx to pistil may accumulate pigments implicated in pollination (
Guerrero ranks as the 4th state in Mexico in terms of biological diversity (
We are grateful to Emmanuel Martínez-Ambriz, an anonymous reviewer, the subject editor Luiza Teixeira-Costa, and the editor in chief Brecht Verstraete for their comments and suggestions to improve this manuscript. This work is part of the MSc thesis of the first author and is financially supported by the National Council of Science and Technology (CONAHCYT) through grant 286670. We thank the curators from the herbaria for allowing access to their collections, particularly to ENCB, HUMO, MEXU, UAGC, and XAL for specimen loans. Special thanks to the Secretaría de Medio Ambiente y Recursos Naturales for granting a collecting permit (SGPA/DGGFS/712/1132/1809/N1-0081/04/18). A sincere and deep gratitude to the brothers Germán†, Hipólito, and Jerónimo Maldonado Marino and their respective families, for their support and company during the fieldwork. Also, our gratitude to the family Solano Moreno from Llanos de Tepoxtepec, especially to the fearless young Santiago. We also thank Dr J.C. Caspeta-Mandujano for his help during fieldwork, Eduardo Santaella for the illustrations, and Elizabeth Skendzic for the final review of the manuscript.