Submitted Successfully!
Thank you for your contribution! You can also upload a video entry or images related to this topic.
Ver. Summary Created by Modification Content Size Created at Operation
1 + 2809 word(s) 2809 2021-08-20 08:11:01 |
2 h Meta information modification 2809 2021-08-31 07:52:27 | |
3 h + 374 word(s) 3183 2021-08-31 07:59:13 | |
4 h + 374 word(s) 3183 2021-08-31 08:00:07 | |
5 format correct Meta information modification 3183 2021-09-28 11:14:38 |

Video Upload Options

Do you have a full video?


Are you sure to Delete?
If you have any further questions, please contact Encyclopedia Editorial Office.
Gutiérrez-Ortega, J.S.; Haynes, J.; Vovides, A.P. Ceratozamia aurantiaca (Zamiaceae). Encyclopedia. Available online: (accessed on 08 December 2023).
Gutiérrez-Ortega JS, Haynes J, Vovides AP. Ceratozamia aurantiaca (Zamiaceae). Encyclopedia. Available at: Accessed December 08, 2023.
Gutiérrez-Ortega, José Said, Jody Haynes, Andrew P. Vovides. "Ceratozamia aurantiaca (Zamiaceae)" Encyclopedia, (accessed December 08, 2023).
Gutiérrez-Ortega, J.S., Haynes, J., & Vovides, A.P.(2021, August 31). Ceratozamia aurantiaca (Zamiaceae). In Encyclopedia.
Gutiérrez-Ortega, José Said, et al. "Ceratozamia aurantiaca (Zamiaceae)." Encyclopedia. Web. 31 August, 2021.
Ceratozamia aurantiaca (Zamiaceae)

Ceratozamia aurantiaca, a new cycad species from Oaxaca, Mexico, is endemic to lowland karst tropical rainforests of the northern mountains (Sierra Norte region).

cycads botanic gardens endangered species

1. Introduction

The cycad genus Ceratozamia Brongn. (Zamiaceae) currently comprises 33 species from Mexico, Guatemala, Belize, and Honduras, with all but three endemic to Mexico [1]. Most species are represented by one to a few narrowly distributed populations separated by a few to several kilometers, generally inhabiting tropical evergreen forest, oak forest, or tropical montane cloud forest [2]. In Ceratozamia, species that are closely related phylogenetically also tend to exhibit geographic proximity and similar morphology [3], which are criteria considered as proxy when testing species delimitation. The species definition within the genus has traditionally been based on morpho-geographic criteria, such that each species is represented by one or more geographically close populations that share morphological characteristics [4][5]. Even so, species delimitation among closely related species has been a constant challenge in Ceratozamia [2][6][7].
Recent reviews of the genus have proposed the recognition of species complexes, which are groups of species with high morphological resemblance [2][8]. Belonging to a species complex in Ceratozamia implies that it can be difficult to correctly identify a member taxon within the complex if detailed information about its origin in the wild is unknown. The C. robusta species complex has been considered one of the most taxonomically difficult groups in the genus [2] (Figure 1). Plants belonging to this species complex are easily recognized by their robust epigeous trunks, large robust cones, large leaves, and petioles that are densely armed with prickles—a set of traits distinct in the genus. Increased interest in cycads in the late 20th century led to the discovery of populations of C. robusta Miq. in the states of Chiapas, Oaxaca, and Veracruz (Mexico), as well as in Guatemala and Belize (Figure 1). Although all populations from these regions share the aforementioned suite of morphological characteristics, a high level of variation among populations of C. robusta sensu lato was previously noted [5] and has only been carefully examined in recent years [7][9][10].
Figure 1. Distribution map of the known populations of Ceratozamia robusta species complex. Black circles surrounded by a dotted line indicate the occurrence of populations of C. robusta, as currently circumscribed. The star symbol indicates the neotype locality of C. robusta (Parque Nacional Cañón del Sumidero, Chiapas, Mexico). Ceratozamia subroseophylla, previously considered as C. robusta, has been recorded in two areas in Santiago Tuxtla, Veracruz, Mexico. The putative new species (herein named Ceratozamia aurantiaca; see results) occurs in two localities in the Sierra Norte region, Oaxaca, Mexico; these populations have been long considered as C. robusta. Green color scale indicates the elevation in meters above sea level (m a.s.l.) as recorded in the raster layers of 30-s resolution of the NASA Shuttle Radar Topographic Mission (SRTM) 90 m Digital Elevation Database v4.1 deposited in DIVA-GIS (, accessed on 15 July 2021).
Martínez-Domínguez et al. [7] (2016) demonstrated that populations from the Los Tuxtlas region of Veracruz, historically recognized as Ceratozamia robusta, were significantly differentiated from other populations of C. robusta. The authors used qualitative morphological traits and molecular evidence to support the erection of a new species that they named C. subroseophylla Mart.-Domínguez & Nic.-Mor. In a similar way, populations from Guerrero (Mexico) reportedly closely related to C. robusta were assigned to a new taxon, C. leptoceras Mart.-Domínguez, Nic-Mor., D.W. Stev. & Lorea-Hern. [9]. Close inspection of morphological variation among populations in Chiapas (Mexico) and Belize revealed that the populations from the Chiapas Highlands (Los Altos de Chiapas), historically recognized as C. robusta, represented yet another different species, C. sanchezae Pérez-Farr., Gut.Ortega & Vovides [10], which has a closer morphological resemblance to the C. miqueliana species complex than to C. robusta. These studies showed that detailed observations and statistical testing of the morphological variation among populations can be used to delimit species within the C. robusta species complex.
In the 1970s, a Ceratozamia population that was considered to be either C. mexicana Brongn., C. mexicana var. robusta (Miq.) Dyer, or C. robusta (according to determinations on herbarium specimens deposited in MEXU, SERO, and HEM), was discovered near the hydroelectric dam “Presa Miguel Alemán” in the Sierra Norte region of Oaxaca (Mexico). Living plants from an early collection at this location, characterized by orange emerging leaves, were introduced into horticulture in the USA, almost exclusively in Florida. The taxon remains in cultivation today, where it is informally known as Ceratozamia sp. “Presa Alemán”. The original locality where the plants were collected was subsequently submerged under the waters of the reservoir upon completion, and accordingly, the taxon was believed to have been rendered extinct. However, further exploration in adjacent areas not affected by the flooding of the Presa Alemán in 2000 resulted in the discovery of more populations with the distinctive orange emergent leaves. In consideration of these new plant records, botanists regarded these populations from the Sierra Norte region as belonging to the C. robusta species complex [2][5] due to their robust trunks, large cones, and large leaves with petioles densely armed with prickles. Observations of plants in situ revealed that they all produce leaves that emerge brown and quickly change to orange (Figure 2). This same coloration occurs ex situ, in a plant cultivated for nearly 30 years at Fairchild Tropical Botanic Garden (FTBG) in Florida, USA, suggesting that this distinctive trait is intrinsic and not due to environmental conditions (Figure A1 and Figure A2).
Figure 2. Emerging leaf color in a Ceratozamia aurantiaca sp. nov. population from San Pedro Teutila, Sierra Norte region, Oaxaca (Mexico). The orange-brown color occurs early in emergence and appears in juveniles (A,B) and adults (C,D).

2. Morphological Observations

Several qualitative traits were identified as exclusive to the putative new species (Table 1). As previously noted in wild plants and botanical garden collections, the orange color of emerging leaves is the most conspicuous unique trait for the plants from the Sierra Norte region, Oaxaca, but it is not the only distinctive trait. In the wild, the trunks of these plants grow erect to decumbent, similarly to C. subroseophylla, whereas they are always erect in C. robusta. Additionally, the texture of leaflets is coriaceous, but papyraceous in the other two species. Other traits observed in the putative new species are shared with either C. robusta or C. subroseophylla: the veins on the abaxial side of the leaflets are not visible in either the putative new species or C. robusta, but are visible in C. subroseophylla, and the apex of the female cone is mucronate in both the putative new species and C. subroseophylla, but acuminate in C. robusta.
Table 1. Comparison of morphological variation among species of the Ceratozamia robusta complex.
Trait C. aurantiaca C. subroseophylla C. leptoceras C. robusta
Trunk Erect to decumbent Erect to decumbent Erect to decumbent Erect
Color of emerging leaves Orange-brown to orange Yellowish-brown Green to copper-green Reddish-brown
Crown of leaves Open Open Open Closed
Texture of leaflets Coriaceous Papyraceous Membranaceous Papyraceous
Veins on abaxial surface of leaflets Not visible Visible Visible Not visible
Apex of female cone Mucronate Mucronate Acute Acuminate

3. Morphometric Analyses

Five of seven measured morphometric traits were found to be significantly differentiated among the three groups at the overall level: length of petiole, number of leaflets, distance between median leaflets, and width of median and basal leaflets (Table 2). The pairwise comparisons allowed the identification of the traits that are significantly differentiated between the putative new species and the two compared species (Table 3). The putative new species has significantly shorter petioles than both C. robusta and C. subroseophylla (Figure 3A), significantly fewer leaflets than C. subroseophylla (Figure 3C), significantly wider spaces between median leaflets than C. robusta and C. subroseophylla (Figure 3E), significantly wider median leaflets than C. robusta and C. subroseophylla (Figure 3F), and significantly wider basal leaflets than C. robusta (Figure 3G). There are no significant differences among groups in length of rachis (Figure 3B) or length of median leaflets (Figure 3D).
Table 2. Morphometric differentiation of seven traits among the three Ceratozamia species examined. Overall differentiation estimated as Welch’s F in ANOVA is indicated. d.f = degrees of freedom. Bold F values indicate significant values, with p < 0.05. The linear discriminant (LD) axis load value of the main axis (which explains 87.79% of the total variation), as estimated in the LD analysis, is annotated. The three highest absolute LD load values of axis 1 are indicated in bold.
Key Name Variable and Unit F d.f. p LD Axis Load
A Length of petiole (cm) 18.27 24.93 1.30 × 10−5 0.309
B Length of rachis (cm) 0.503 23.15 0.6112 −0.024
C Number of leaflet pairs 12.53 24.81 0.0001735 0.103
D Length of median leaflets (mm) 1.682 21.84 0.2092 0.032
E Distance between median leaflets (mm) 12.56 23.87 0.0001877 −0.278
F Width of median (mm) 20.94 24.59 4.899 × 10−6 −0.227
G Width of basal leaflets (mm) 7.277 22.46 0.003662 −0.033
Table 3. Pairwise Tukey’s Q values of differentiation between species of seven morphometric traits. Abbreviations: traits A-G correspond to those listed in Table 3. * = p < 0.05, ** = p < 0.005, *** = p < 0.001.
  C. aurantiaca vs.
C. robusta
C. aurantiaca vs.
C. subroseophylla
C. subroseophylla vs.
C. robusta
A (length of petiole) 4.121 * 9.492 *** 5.371 **
B (length of rachis) 1.247 0.4368 0.8097
C (number of leaflet pairs) 3.066 7.815 *** 4.749 **
D (length of median leaflets) 1.317 0.927 2.244
E (distance between median leaflets) 3.804 * 7.942 ** 4.138 *
F (width of median leaflets) 8.635 *** 6.692 *** 1.942
G (width of basal leaflets) 4.287 * 0.4224 3.864 *
The LDA summarized the total morphometric variation into two main axes, explaining 87.79% and 12.21% of the total variation, respectively (Figure 4). Three trait groups were found to be completely non-overlapping, as denoted by the biplots in Figure 4 (load values are listed in Table 2): petiole length (trait A), number of leaflets (trait C), and space between median leaflets (trait E). The confusion matrix obtained from the LDA (Table 4) shows that most individuals were estimated to belong to their given groups, as expected; only one individual of the putative new species might be confused with C. robusta, and only two individuals of C. robusta might be confused with the putative new species. However, the Mahalanobis distances among the three groups were estimated to be highly significant (Table 5), suggesting that the total variation completely sorted between the assigned groups.
Table 4. Confusion matrix constructed with the linear discriminant analysis (LDA). Rows indicate given groups (number of individuals considered Ceratozamia aurantiaca, C. robusta, or C. subroseophylla according to their population type) and columns indicate groups predicted by the LDA.
  C. aurantiaca C. robusta C. subroseophylla Total
C. aurantiaca 15 1 0 16
C. robusta 2 18 0 20
C. subroseophylla 0 0 11 11
Total 17 19 11 47
Table 5. Squared Mahalanobis distances (below diagonal) and p-values (above diagonal) among the three analyzed species. All values are significant (p < 0.001), suggesting complete sorting among species’ variation.
  C. aurantiaca C. robusta C. subroseophylla
C. aurantiaca - 5.07 × 10−6 7.42 × 10−8
C. robusta 10.26 - 1.80 × 10−5
C. subroseophylla 7.35.56 13.32 -
In summary, the following evidence is presented to support the putative new species described herein: (1) Distinctive qualitative morphological traits distinguish the populations of the Sierra Norte region from C. robusta and C. subroseophylla, the two most closely related taxa. The main distinctive trait is the orange color of emerging leaves (Figure 2). This characteristic can also be observed in plants in cultivation (Figure A1), discarding the alternative explanation that it is due to environmental factors. (2) Significant morphometric differentiation in most of the examined traits distinguishes the populations of the Sierra Norte region from other species in the C. robusta species complex.

4. New Species Description

Ceratozamia aurantiaca Pérez-Farr., Gut.-Ortega, J.L.Haynes & Vovides sp. nov. (Figure 5, Figure 6 and Figure 7).
Figure 5. Ceratozamia aurantiaca sp. nov. (A) Adult plant with orange emerging leaves beginning to transition to green. (B) Adult plant with erect trunk. (C,D) Details of leaflet articulation, prickles, and leaflet shape. (E) Details of apex and heavily armed petioles.
Figure 6. Strobili of Ceratozamia aurantiaca sp. nov. (A) Microstrobilus; (B) megastrobilus.
Figure 7. Mature megastrobilus of Ceratozamia aurantiaca sp. nov., showing details of megasporophylls and peduncle (A), mucronate apex (B) and view from below (C). Scale = 10 cm. Photos by José García.
Holotype:—MEXICO. Oaxaca, Sierra Norte, San Pedro Teutila, 30 May 2021, Pérez-Farrera M.A & Díaz-Jiménez p. 4014 ♀ (HEM!). Isotypes: (XAL).
Ceratozamia aurantiaca is easily distinguished by its emerging leaves of orange color that turn green at maturity. It resembles C. robusta, but has longer petioles and wider separation between leaflets along the rachis.
Additional specimens examined:—MEXICO. Oaxaca: Santa Maria Tlalixtac, 675 m a.s.l. (above sea level), 26 November 2004, Gonzalo Juárez García & Cutberto Ángel Cruz Espinosa 868 (MEXU, SERO); Chiquihuitlán de Benito Juárez, 861 m a.s.l., 26 November 2004, Cutberto Ángel Cruz Espinosa & Gonzalo Juárez García 1945 (MEXU, SERO); San Pedro Teutila, 708 m a.s.l., 10 June 2004, Gonzalo Juárez García & Laura Escobar 425 (MEXU, SERO); 588 m a.s.l., 30 May 2021, Miguel Ángel Pérez-Farrera & Pedro Díaz-Jiménez 34,015 ♂ (MEXU; HEM).
Plant rupicolous, arborescent, unbranching. Stem cylindrical, erect, sometimes decumbent with age, 20–150 cm tall, 10–15 cm in diameter, covered with persistent leaf bases. Cataphylls persistent, triangular, brown, densely tomentose at emergence, apex acuminate. Leaves pinnate, 10–27 per apex (mean = 15), crown open, erect, ascending, eventually arching at maturity, basally slightly keeled, 117–257 cm long, 53–77 cm wide, reddish-light brown at emergence, becoming bright orange, and then green at maturity. Petiole terete 31–73 cm long (mean = 54 cm), densely armed with thick prickles. Rachis terete, 85–187 cm long (mean = 135 cm), with spaced prickles diminishing apically, green at maturity. Leaflets coriaceous, linear to subfalcate, occasionally sigmoid, 19–31 pairs (mean = 25), subopposite basally, opposite medially, margin entire, apex asymmetric, acute to acuminate; base broad attenuate, articulation brownish to green, depending on age; veins 29–37, parallel, inconspicuous, slightly translucent; median leaflets 21–38 cm long (mean = 33 cm), 3.4–4.7 cm wide (mean = 4.0 cm), 2.4–4.7 cm between leaflets (mean = 3.5 cm), articulation 0.75–1.5 cm wide (mean = 1.0 cm). Microstrobilus solitary, cylindrical, erect, 34–36 cm long, 4–6 cm diameter, light-orange and tomentose when emerging, light brown when mature, peduncle 4.5–7.5 cm long, 1.2–1.9 cm diameter, densely tomentose. Microsporophyll cuneiform, distal face bicornate, 16–25 mm long, 7–13 mm wide, sporangia zone on abaxial surface 11–20 mm long, microsporangia grouped in sori of 3–4. Megastrobilus solitary, cylindrical, erect, 39–42 cm long, 10.3–10.7 cm diameter, light-orange pubescent base color with green diamond-shaped patches and dark brown trichomes on megasporophyll terminal facets at emergence, maturing light-orange with greenish-yellow horizontal line and brown trichomes on megasporophyll terminal facets; apex mucronate, peduncle 7–8.8 cm long, 1.8–1.9 cm in diameter, tomentose. Megasphorophylls peltate, bicornate, 3–4.25 cm wide, 1.7–2.4 cm tall, distal face pubescent, brown to reddish-orange (including horns) at maturity, base green with light-orange pubescence; peduncle tomentose, light green when immature, light brown at maturity. Seeds ovoid, sarcotesta cream when immature, orange-brown when mature, sclerotesta beige, 2.3–2.7 cm diameter, 1.6–1.9 cm long, with micropylar ridges.
Habitat description: Ceratozamia aurantiaca grows in karst tropical forests or Pinus-Quercus forests, between 200 to 800 m a.s.l.
Etymology: The specific epithet is from the Latin “aurantiacus” and refers to the glowing orange color of emerging leaves.

3. Ceratozamia aurantiaca

Ceratozamia aurantiaca possesses a set of diagnosable traits that separates it from its congeners with which it might be confused: orange emergent leaves, shorter petioles, wider median leaflets, and wider spacing between median leaflets. It also possesses a suite of additional traits that, combined with the above-mentioned traits and taken as a whole, distinguish it from all other species in the genus: leaves ascending, with numerous robust, large, medium, and small, recurved to barbed, green prickles on the petiole; coriaceous, leaflets lanceolate in shape, symmetrical to slightly asymmetrical, linear to subfalcate (occasionally slightly sigmoid), with wide articulations; large megasporangiate strobilus with orange base color, green coloration localized to the terminal facet of the megasporophylls, and numerous dark trichomes.
The distinction of Ceratozamia aurantiaca as a new species helps resolve the definition of C. robusta. Historically, all populations sharing characteristics of the C. robusta species complex (large trunks, large cones, and large leaves with prickled petioles) from Chiapas, Belize, Guatemala, and Oaxaca were assumed to be C. robusta. However, recent studies [7][9][10] have suggested that C. robusta, as defined by the neotypification by Stevenson & Sabato [6], seems to be restricted to the eastern portion of the distributional range (Chiapas, Belize, and Guatemala), whereas the populations from Oaxaca and Guerrero might represent a group of closely related species. Ceratozamia leptoceras seems to be the most dissimilar when compared with the species covered in this study (Table 1), as it has thin prickles on the petioles (thick in the other species), linear leaflets with membranaceous texture (lanceolate and papyraceous or coriaceous in the other species), and an acute megastrobilus apex (acuminate or mucronate in other species).
The species comprising the C. robusta species complex occur in mesic habitats, usually rainforests considered floristic refugia during the Neogene glaciations [11]. Such areas are currently separated by drier valleys or high mountains that may represent geographic barriers against gene flow (Figure 1). These patterns of distribution suggest that the Ceratozamia species are products of geographic isolation leading to allopatric speciation, as has been demonstrated in another cycad species in this geographic area [12]. After gaining geographic isolation, cycads seem to be prone to experience local adaptation through the retention/acquisition of anatomical features [8][13] and stochastic, demographic processes [12][14]. Ceratozamia aurantiaca is likely to have originated through similar evolutionary processes.
Pigment variation in emerging leaves has been well documented in Ceratozamia. Whitelock [15] mentioned that emerging leaves in the species belonging to the Ceratozamia miqueliana species complex (e.g., C. miqueliana H.Wendl., C. euryphyllidia Vázq.Torres, Sabato & D.W.Stev., C. becerrae Pérez-Farr., Vovides & Schutzman) always produce lime-green emergent leaves, a trait that can be considered as diagnostic in this group. Other Ceratozamia species may also produce a brownish pigmentation that may vary from yellowish-brown (as in C. subroseophylla) to a more common reddish-brown color, as in C. sanchezae or C. robusta. In populations of these latter species, it is common to find individuals producing either green or reddish-brown emerging leaves. On the other hand, the northern species (e.g., C. latifolia Miq., C. zaragozae Medellín, C. chamberlainii Mart.-Domínguez, Nic.-Mor. & D.W.Stev.) always produce emerging leaves of brownish to reddish color. The presence of the orange color in emerging leaves of C. aurantiaca is unique in the genus. This distinctive trait is present in wild plants (Figure 2) and in plants living in garden conditions for nearly 30 years (Figure A1 and Figure A2), suggesting that it has a genetic background, rather than environmental. The fixed expression of pigments that produce the orange color in emerging leaves may be the result of stochastic, demographic processes (a combination of population bottlenecks and the random fixation of alleles due to genetic drift).
To date, three populations of Ceratozamia aurantiaca are known in the wild (Figure 1), in the municipalities of San Pedro Teutila and San Bartolomé Ayautla, Oaxaca. Populations have a narrow distribution and have suffered burning and clearing due to livestock activities. There are approximately 50 adult plants in San Bartolomé Ayautla, and close to 200 adult plants in San Pedro Teutila; thus, this species should be considered as “threatened with extinction” (P) in the Mexican Official Norm NOM-059-ECOL (SEMARNAT 2010) and as “Endangered” according to the IUCN Red List of Threatened Species (2021), based on the criteria A2ce+4c; C1. Further studies of more populations from Oaxaca and phylogenetic analyses at the genus level, as performed on other cycad genera in Mexico [16][17], will further clarify the species and genetic diversity in Ceratozamia, the delimitation within the C. robusta species complex, and the evolutionary history of the cycad genus Ceratozamia.


  1. Calonje, M.; Stevenson, D.W.; Osborne, R. The World List of Cycads, Online Edition. 2021. Available online: (accessed on 4 August 2021).
  2. Vovides, A.P.; Pérez-Farrera, M.A.; González, D.; Avendaño, S. Relationships and Phytogeography in Ceratozamia (Zamiaceae). In Cycad Classification: Concepts and Recommendations; Walters, T., Osborne, R., Eds.; CABI Publishing: Wallingford, UK, 2004; pp. 109–125.
  3. Medina-Villarreal, A.; González-Astorga, J.; de Los Monteros, A.E. Evolution of Ceratozamia cycads: A proximate-ultimate approach. Mol. Phylogen. Evol. 2019, 139, 106530.
  4. Walters, T.; Osborne, R.; Decker, D. ‘We Hold These Truths…’. In Cycad Classification: Concepts and Recommendations; Walters, T., Osborne, R., Eds.; CABI Publishing: Cambridge, UK, 2004; pp. 1–11.
  5. Whitelock, L.M. The Cycads; Timber Press: Portland, OR, USA, 2002; p. 532.
  6. Stevenson, D.W.; Sabato, S. Typification of names in Ceratozamia Brongn., Dion Lindl., and Microcycas A. DC. (Zamiaceae). Taxon 1986, 35, 578–584.
  7. Martínez-Domínguez, L.; Nicolalde-Morejón, F.; Vergara-Silva, F.; Stevenson, D.W. Integrative taxonomy of Mexican cycads: Biogeography, morphology and DNA barcoding corroborate a new sympatric species in Ceratozamia (Zamiaceae). Phytotaxa 2016, 268, 25–45.
  8. Vovides, A.P.; Pérez-Farrera, M.A.; Gutiérrez-Ortega, J.S.; Avendaño, S.; Medina-Villarreal, A.; González-Astorga, J.; Galicia, S. A revision of the Ceratozamia miqueliana (Zamiaceae) species complex based on analyses of leaflet anatomical characters. Flora 2020, 270, 151649.
  9. Martínez-Domínguez, L.; Nicolalde-Morejón, F.; Lorea-Hernández, F.G.; Vergara-Silva, F.; Stevenson, D.W. A novelty in Ceratozamia (Zamiaceae, Cycadales) from the Sierra Madre del Sur, Mexico: Biogeographic and morphological patterns, DNA barcoding and phenology. PhytoKeys 2020, 156, 1.
  10. Gutiérrez-Ortega, J.S.; Pérez-Farrera, M.A.; Vovides, A.P.; Chávez-Cortázar, A.; López, S.; Santos-Hernández, N.G.; Ruíz-Roblero, S.K. Ceratozamia sanchezae (Zamiaceae): A new cycad species from Chiapas Highlands (Mexico). Phytotaxa 2021, 500, 201–216.
  11. Wendt, T. Las selvas de Uxpanapa, Veracruz-Oaxaca, México: Evidencia de refugios florísticos cenozoicos. An. Inst. Biol. UNAM Ser. Bot. 1989, 58, 29–54.
  12. Gutiérrez-Ortega, J.S.; Salinas-Rodríguez, M.M.; Ito, T.; Pérez-Farrera, M.A.; Vovides, A.P.; Martínez, J.F.; Molina-Freaner, F.; Hernández-López, A.; Kawaguchi, L.; Nagano, A.J.; et al. Niche conservatism promotes speciation in cycads: The case of Dioon merolae (Zamiaceae) in Mexico. New Phytol. 2020, 227, 1872–1884.
  13. Gutiérrez-Ortega, J.S.; Yamamoto, T.; Vovides, A.P.; Pérez-Farrera, M.A.; Martínez, J.F.; Molina-Freaner, F.; Watano, Y.; Kajita, T. Aridification as a driver of biodiversity: A case study for the cycad genus Dioon (Zamiaceae). Ann. Bot. 2018, 121, 47–60.
  14. Gutiérrez-Ortega, J.S.; Molina-Freaner, F.; Martínez, J.F.; Pérez-Farrera, M.A.; Vovides, A.P.; Hernández-López, A.; Tezuka, A.; Nagano, A.J.; Watano, Y.; Takahashi, Y.; et al. Speciation along a latitudinal gradient: The origin of the Neotropical cycad sister pair Dioon sonorense-D. vovidesii (Zamiaceae). Ecol. Evol. 2021, 11, 6962–6976.
  15. Whitelock, L.M. Range and variation in the genus Ceratozamia (Zamiaceae). Bot. Rev. 2004, 70, 235–239.
  16. Calonje, M.; Meerow, A.W.; Griffith, M.P.; Salas-Leiva, D.; Vovides, A.P.; Coiro, M.; Francisco-Ortega, J. A time-calibrated species tree phylogeny of the New World cycad genus Zamia L. (Zamiaceae, Cycadales). Int. J. Plant Sci. 2019, 180, 286–314.
  17. Gutiérrez-Ortega, J.S.; Salinas-Rodríguez, M.M.; Martínez, J.F.; Molina-Freaner, F.; Pérez-Farrera, M.A.; Vovides, A.P.; Matsuki, Y.; Suyama, Y.; Ohsawa, T.A.; Watano, Y.; et al. The phylogeography of the cycad genus Dioon (Zamiaceae) clarifies its Cenozoic expansion and diversification in the Mexican transition zone. Ann. Bot. 2018, 121, 535–548.
Subjects: Plant Sciences
Contributors MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to : , ,
View Times: 487
Revisions: 5 times (View History)
Update Date: 28 Sep 2021