Micromorphology of the flower of Zephyranthes lindleyana (Amaryllidaceae)

Modern Phytomorphology

All submissions of the EM system will be redirected to Online Manuscript Submission System. Authors are requested to submit articles directly to Online Manuscript Submission System of respective journal..

Research - Modern Phytomorphology ( 2021) Volume 15, Issue 2

Micromorphology of the flower of Zephyranthes lindleyana (Amaryllidaceae)

O. Fishchuk*
Lesia Ukrainka Volyn National University, Pr. Voli. 13, Lutsk, 43025, Ukraine
*Corresponding Author:
O. Fishchuk, Lesia Ukrainka Volyn National University, Pr. Voli. 13, Lutsk, 43025, Ukraine, Tel: 380663108107, Email:

Received: 12-Mar-2021 Accepted: 26-Mar-2021 Published: 03-Apr-2021, DOI: 10.5281/zenodo.5078277


In connection with the search for new morphological features, useful for the taxonomy of plants was studied the structure of the flowers of the Zephyranthes lindleyana Herb. (Mexico), as modern molecular taxonomy does not always consider the morphological and anatomical features of the flower, and the vertical zonality of the gynoecium does not take into account at all. The morphometric parameters and micromorphology of the ovary were described by using flowers transverse sections. 10 flowers of Z. lindleyana were sectioned using standard methods of Paraplast embedding and serial sectioning at 20 mkm thickness. Sections were stained with Safranin and Astra Blau and mounted in Eukitt. We investigated the presence of three vertical zones in the Z. lindleyana gynoecium: synascidiate, symplicate and hemisymplicate. Asymplicate zone is absent. The data we obtained helped deepen the knowledge on micromorphological peculiarities of flowers of Z. lindleyana and will help to compare the received morphological and anamomical features with features studied earlier for representatives of Amaryllidaceae family for use them in the taxonomy in future.


Zephyranthes lindleyana, ovary, vertical zones, gynoecium, micromorphology, septal nectary


The integration of molecular phylogenetic data and evolutionary comparative morphology of a flower is a promising direction for the construction of a modern evolutionary system of orders, families, subfamilies and genera. The study of vascular anatomy and micromorphology of monocotyledonous flowers is a current way in the study of evolutionary morphology (Skrypec and Odintsova 2020; Fishchuk and Odintsova 2017). The object of our study was selected Z. lindleyana, which is widely grown as an ornamental flowering plant. Genus Zephyranthes Herb. belongs to the subtribe Hippeastrinae Walp tribes Hippeastreae Sweet., subfamily Amaryllidoideae s.s., family Amaryllidaceae (Chase et al. 2016). The alkaloids study of Zephyranthes is presented (Centeno-Betanzos et al. 2021), the endosperm development and the variations of structures of embryo sacs was studied (Chengqi 2019). The purpose of our study is to clarify the features of floral morphology and internal gynoecium structure, the structure of septal nectaries and to determine the vertical zonality of gynoecium in family members of the family Amaryllidaceae.

Materials and Methods

Plant material was collected in the A.V. Fomin Botanical garden of Taras Shevchenko National University of Kyiv and fixed in 70% alcohol. For light microscope observations, 10 flowers Z. lindleyana were sectioned using standard methods of Paraplast embedding and serial sectioning at 20 mkm thickness by Barykina et al. (2004). This is about 200 slides and about 7200 serial sections. Sections were stained with Safranin and Astra Blau and mounted in Eukitt. Digital photomicrographs were made using a microscope AMSCOPE T490B-10M (USA) and microscope digital camera AMSCOPE 10MP MU1000 (USA). The height of the gynoecium vertical zones was obtained after the calculation of the transverse sections of the pistil. We used the concept of vertical zonation of gynoecium by W. Leinfellner (Leinfellner 1950) to analyze the internal structure of the gynoecium, which takes into consideration only the congenital fusion of the carpels. The methodological basis of the vertical zonation gynoecium study was formulated by W. Leinfellner, later the method was elaborated for monocots (Odintsova 2013).


Z. lindleyana flowers are up to 6.6 cm-7 cm long, slightly zygomorphic, pink. The scape is 12.5 cm-13 cm long and 0.4 cm-0.5 cm in diameter, flowers are solitary. Two bracts are conical, fused into one, forming a twokeel structure about 4 cm long, 1.3 cm wide and 0.9 cm at the base, leathery, brown. The pedicel is up to 1.8 cm long, about 0.3 cm in diameter (Fig. 1A-B). Perigonium is simple with linear members. The flower is tube funnelshaped, the flower tube is about 2.4 cm long, 0.4 cm in diameter at the base and 0.8 cm above the base (Fig. 1G). The outer tepals are wider than the inner tepals. The outer tepals are 5.2 cm, 5 cm, 5.2 cm long and 1.9 cm, 1.8 cm, 1.9 cm wide, and the inner tepals are 4.9 cm, 4.9 cm, 5 cm in length and 1.4 cm, 1.5 cm, 1.4 cm wide, respectively. The androecium is characterized by the presence of 6 stamens, which are attached to the base of the flower tube. The length of the inner stamens is 3.3 cm, and the length of the outer stamens is 3 cm. The stamens are straight, tapering to the top, the stamens of the outer circle are 2.3 cm, and the length of the stamens of the inner circle is 2.6 cm, 0.1 cm are the stamens in diameter. Anthers bent at the apex, introse, dorsifixed (Fig. 1H). Anthers of external and internal stamens are 1.3 cm long. But the filaments are attached at different heights to the anther in the external and internal stamens (Fig. 1H). Anthers, 0.1 cm in diameter, are attached just below the middle of the anther height.


Figure 1: Ascending series of transversal sections of the flower Zephyranthes lindleyana. Scale bar 500 µm; A, B: Pedicel; C, E: Inferior ovary; C, D: Symplicate zone; E,F: Hemysymplicate zone; G: Flower tube and style; H: Free tepals, filaments and style; dv: dorsal vein; fi: filament; lo: ovary locule; ft: flower tube; ov: ovule; sc: style channel; sv: septal vein; st: style; te: tepal; vb: vascular bundle; vv: ventral vein.

The gynoecium is represented by three growing carpels. The length of the gynoecium is 6 cm, the ovary is ovoid, bright green 0.8 cm high and 0.4 cm in diameter (Fig. 1D), which turns into a slightly zygomorphic, green at the base, and above the white, s-shaped style 5 cm long and 0.1 cm in diameter (Fig. 1H). Stigma is three-lobeles, with widely curved lobeles 0.2 cm long and 0.1 cm in diameter. The fruit is a capsule with flattened black seeds.

In Z. lindleyana gynoecium we distinguish the following structural zones: synascidiate structural zone, height about 360 μm and fertile symplicate structural zone, the height of which is about 2080 μm (Fig. 1C-1D) and hemisymplicate zone is about 2500 μm (Fig. 1E-1F). Septal nectaries appear in the hemisymplicate zone and open with nectary slits at the base of the style, the total height of the septal nectary is 2900 μm (Fig. 1F). The roof of the ovary is 400 microns.


Characteristic features of the genus Zephyranthes is a hollow scape, terete, rarely retained entirely inside the bulb, single-flowered, spathe bracts fused and tubular below the middle (Meerow and Snijman 1998). According to E. Daumann (Daumann 1970), the genus Zephyranthes has an internal septal nectary. He established the presence of epidermal septal nectaries in Z. lindleyana. We found three vertical zones in the ovary of the studied species: synascidiate, symplicate and hemisymplicate. Septal nectaries appear in the hemisymplicate zone. In Hippeastrum striatum gynoecium were found synascidiate, symplicate and hemisymplicate vertical zones (Fishchuk 2021).


The study of the micromorphology of Z. lindleyana, showed the presence of three vertical zones in the ovary synascidiate, symplicate and hemisymplicate, lengthy septal nectary that appear at the hemisymplicate zone and are continued by nectary cavities. Flower morphology and gynoecium structure will help us to differentiate the studied species and their morphological and anatomy features from other members of the Amaryllidaceae family.


Barykina R.P., Veselova T.D., Deviatov A.G., Djalilova H.H., Iljina G.M., Chubatova N.V. (2004). Handbook of the botanical microtechniques. Moscow: Izd-vo MGU.

Centeno-Betanzos L.Y., Reyes-Chilpa R., Pigni N.B., Jankowski C.K., Torras-Claveria L.,  Bastida J. (2021). Plants of the ‘Libellus de Medicinalibus Indorum Herbis’ from Mexico, 1552. Zephyranthes fosteri (Amaryllidaceae) Alkaloids. Chem Biodiversity 18: e2000834.

Chase M.W., Christenhusz M.J.M., Fay M.F., Byng J.W., Judd W.S., Soltis D.E., Stevens P.F. (2016). An update of the angiosperm phylogeny group classification for the orders and families of flowering plants: APG IV. Botan J Linnean Soc 181: 1-20.

Ao C. (2019). The endosperm development and the variations of structures of embryo sacs: unravelling the low fecundity of Zephyranthes candida (Amaryllidaceae). Plant Biosyst Internat J Dealing Aspects Plant Biol 153: 673-678.

Daumann E. (1970). Das Blütennektarium der Monocotyledonen unter besonderer Berücksichtigung seiner systematischen und phylogenetischen Bedeutung. Feddes Repertorium 80: 463-590.

Fishchuk O. (2021). Comparative flower morphology in Hippeastrum striatum (Lam.) HE Moore (Amaryllidaceae). Ukr J Ecol 11: 273-278.

Fishchuk O.S., Odintsova A.V. (2020). Micromorphology and anatomy of the flowers of Galanthus nivalis and Leucojum vernum (Amaryllidaceae). Regulat Mech Biosyst 11: 463-468.

Leinfellner W. (1950). Der Bauplan des synkarpen Gynözeums. Österreichische Botanische Zeitschrift 97: 403-436.

Meerow A.W., Snijman D.A. (1998). Amaryllidaceae In K. Kubitzki [ed.], Families and genera of vascular plants. Springer pp: 83-110.

Odintsova A. (2013). Dva osnovnyx typy septalnyx nektarnykiv odnodolnyx. Visnyk Lvivskogo universytetu. Seriya biologichna 61: 41-50.  

Odintsova A., Fishchuk O. (2017). The flower morphology in three Convallariaceae species with various attractive traits. Acta Agrobotanica 70.

slot demo