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Analele ştiinţifice ale Universităţii “Al. I. Cuza” Iaşi<br />

Tomul LIV, fasc. 2, s.II a. <strong>Biologie</strong> vegetală, 2008<br />

MICROSPOROGENESIS AND THE MALE GAMETOPHYTE AT EPHEDRA<br />

DISTACHYA L.<br />

GENŢIANA MIHAELA IULIA PREDAN * , IRINA GOSTIN **<br />

Abstract: This study <strong>de</strong>scribes the microsporogenesis and the male gametophyte in Ephedra distachya L., only<br />

one species of the Ephedraceae family growing spontaneous in Romania. Ephedra distachya L. is a dioecious<br />

plant. Light microscopy (lm) is used to examine the early <strong>de</strong>velopmental stages of the male cones and<br />

combined light (lm) and scanning electron microscopy (sem) were used to analyze the mature pollen grains.<br />

The pollen cones are clustered at no<strong>de</strong>s either sessile or stalked. They are oval-oblong, each is composed of 2-8<br />

<strong>de</strong>cussate pairs of membranous bracts, proximal bracts empty; each distal bract subtending a male flower<br />

composed of 2 basally fused, orbicular or obovate scales (false perianth); sessile anthers on staminal column.<br />

Ephedra distachya pollen is particularly abundant. Ephedra distachya has the polyplicate pollen type<br />

characterized by a pointed-oval shape and 6 longitudinal ridges and 6 valleys, due to alternation of thicker and<br />

thinner exine regions, inaperturate. In polar view, ridges are low and triangular. On the SEM analysis the pollen<br />

wall of Ephedra distachya is simple, so the SEM closely resembles the LM observation.<br />

Key words: Ephedra distachya L., male cones, pollen <strong>de</strong>velopment<br />

Introduction<br />

Genus Ephedra L. contains 35-45 species, most of them populating the <strong>de</strong>sert or arid<br />

regions. In Romania a single species of Ephedraceae family occurs - Ephedra distachya L. Its<br />

status is rare [12].<br />

Genus Ephedra L. has been much studied from the morphological and anatomical point<br />

of view, information was summarized and inclu<strong>de</strong>d in synthesis works [8, 10, 14, 15, 16]. The<br />

histology of the flowers and strobili of the Ephedra distachya L. plants was examined by Van<br />

Tieghem (1869), Thoday and Berridge (1912) [10], later by Favre-Duchartre M. [5]. Baranec T.<br />

Rehorek and V. studied the reproductive cycle of the Ephedra distachya L. plants, spontaneous<br />

in Slovakia [2] and P. Mehra N. analysed dimensions of the male nuclei of the representatives<br />

in the Ephedra genus [10].<br />

Allison S. D. et al. have studied all the important stages of the Ephedra pollen<br />

<strong>de</strong>velopment using both photonic and the scanning and transmission electronic microscope [3].<br />

Gamal El-Ghazaly et al. were concerned about pollen grain polarity, the aperture situation and<br />

the pollen tube at 5 species of Ephedra including E. distachya L. [6].<br />

The microsporogenesis and the <strong>de</strong>scription of the pollen and the male gametophyte<br />

* University of Bucharest, Faculty of Biology, Department <strong>de</strong> Botany and Microbiology, Aleea Portocalelor, nr. 1-3,<br />

060101, Bucureşti, Romania; ggentiana@yahoo.com<br />

** „Al. I. Cuza” University, Faculty of Biology, Bd. Carol I, no. 20A, 700506, Iaşi, Romania; irinagostin@yahoo.com<br />

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<strong>de</strong>velopment in Ephedra distachya L. provi<strong>de</strong>s interesting characterization in this species.<br />

Material and methods<br />

Our study was carried out on samples of Ephedra distachya L. from different places in<br />

Romania: Agigea Marine Dune Reserve (Constanta County), Culmea Pricopanului (Tulcea<br />

County), the Botanical Gar<strong>de</strong>n of Iaşi (cultivated plants) and from Bulgaria (Balchik) [7, 8].<br />

Ephedra distachya L. is a dioecious plant. Male cones were collected during the three spring<br />

months (March, April and May), in successive phaenological phases, from the cones initiation<br />

up to the pollen shedding.<br />

The biological material (male cones) was fixed in 70% alcohol or FAA (formalin 40%, 5<br />

cc: alcohol 70%, 90 cc: glacial acetic acid 5 cc). After being fixed, the material has been<br />

processed in accordance with the paraffin embeding protocol [3], sectioned (transverselly and /<br />

or longitudinally) with a Minot type microtome at 12-15 μm thick, colored with Ehrlich’s<br />

haematoxylin and embed<strong>de</strong>d in Canada balm. To highlight microspores and young pollen grains<br />

microscopical preparations squash type have been ma<strong>de</strong>, that have been colored with acetic<br />

carmine.<br />

All obtained sections were analyzed using light microscope (LM) Docuval type and<br />

photographed with a digital photo camera slr Canon EOS 400D. For the analysis of the pollen<br />

grains at electronic scanning microscope (SEM) a Vega - TESCAN LSH microscope was used<br />

in The Faculty of Biology of The “Al I. Cuza” University from Iaşi [12].<br />

Male cones were consi<strong>de</strong>red from the morphological point of view with a Belphotonics<br />

stereomicroscope and photographed with the same digital camera.<br />

The <strong>de</strong>scription of the pollen grains has been ma<strong>de</strong> in accordance with the terminology<br />

adopted by Faegri [4].<br />

Results and discussions<br />

The male cones, either sessile or stalked, are found clustered at no<strong>de</strong>s (fig. 1). The male<br />

cones are green, oval-oblongue, each of them being composed of 2-8 <strong>de</strong>scussate pairs of<br />

membranous bracts, like cups (Fig. 2, 3). The lower pair bracts is sterile, each distal bract<br />

subtending a male flower composed of 2 basally fused, orbicular or obovate scales (primitive<br />

periant) (Fig. 4, 7), an axis (microsporangiophore or anterophore) terminal bearing a number of<br />

anthers, each anther with two micro sporangia (pollen sacs) (Fig. 4). A group of archespores<br />

subepi<strong>de</strong>rmal cells in the mature cones is observed in March (fig. 5).<br />

In April, following meiosis I, macrospore dyads have resulted. After meiosis II numerous<br />

tetrads of microspores appear, the wall formation taking place after each stage of meiosis. Soon,<br />

the wall surrounding the 4 microspore cells dissolve and the microspores in the pollen sac are<br />

25


eleased. The microsporangia wall is composed of three known layers: epi<strong>de</strong>rmis, the median<br />

layer and the tapetum layer. The median layer is composed of a single row of parenchimatic<br />

cells and, as the pollen sac grows, its cells are flattened so that they ultimately disappear. The<br />

tapetum has signs of <strong>de</strong>generation after the reductional division (Fig. 6) and no longer in the<br />

stage of mature pollen (Fig. 8). At mature pollen sac epi<strong>de</strong>rmis persists. Its cells have a regular<br />

appearance and their walls are thickened (Fig. 9). Only in a small portion of the pollen sac<br />

upper part a few parenchimatic cells with thin walls remain. By their breaking a hole will form<br />

that will be issued pollen (porici<strong>de</strong> opening).<br />

In May, the pollen is divi<strong>de</strong>d and forms a small prothalian cell and a large, central one<br />

(Fig. 10). The last divi<strong>de</strong> and formed the second prothalian cell and initial anteridial cell. The<br />

last divi<strong>de</strong> and give a vegetative larger cell, and a generative cell. The generative cell will form<br />

the stalk cell and spermatogene cell, the latter giving rise to gametes. Regarding pollen sacs, the<br />

pollen has 5 cells [8]. The mature pollen grains are yellow, fusiforme and obvious poliplicate:<br />

they have 6 longitudinal ridges (plicae) (sometimes slightly corrugated) and 6 valleys, formed<br />

due to the alternation of thicker and thinner exine regions (Fig. 9, 10). On a polar view, the<br />

ridges are short and triangular. Pollen grains have 53 μm long axis and 20 μm short axis. At the<br />

electronic scanning microscope (SEM), the pollen surface is no obvious regulate and no<br />

aperture was noticed eather, so the pollen is inaperturate (Fig. 11, 12).<br />

Conclusions<br />

In March, a group of archespore cells appears in the pollen sacs, subepi<strong>de</strong>rmaly.<br />

In April the anther wall is composed of an epi<strong>de</strong>rmis and a scrap tapetum and the<br />

microspores are free.<br />

In May the anther wall is only represented by the epi<strong>de</strong>rmis and numerous grains of<br />

fusiforme and yellow pollen are found insi<strong>de</strong> the pollen sac, in our observation (in 17 May 2007<br />

on Culmea Pricopanului) the pollen grains are uninucleate.<br />

According to the SEM observations, the pollen grains of Ephedra distachya L. have a<br />

simple structure, the SEM observations being very similar to those ma<strong>de</strong> on an optical<br />

microscope.<br />

REFERENCES<br />

1. ANDREI M., RĂDULESCU D., 1972 - Caiet pentru tehnica preparării şi conservării materialului biologic.<br />

Tipogr. Univ. din Bucureşti<br />

2. BARANEC, T., V. REHOREK, et al., 1994 - Generative reproduction of ephedra (Ephedra distachya L.) in<br />

Slovakia. Biologia Bratislava, 49 (1): 65-67<br />

3. DOORES ALLISON S., OSBORN J. M., GAMAL EL-GHAZALY., 2007 - Pollen Ontogeny in Ephedra<br />

americana (Gnetales). International Journal of Plant Sciences 168 (7): 985-997<br />

4. FAEGRI K., IVERSEN J., 1966 - Textbook of pollen analysis. 2nd Ed. Munksgaard, Copenhagen<br />

26


5. FAVRE-DUCHARTRE M., 1959 - Contribution à l’étu<strong>de</strong> <strong>de</strong> la reproduction sexuée chez Ephedra distachya. C.<br />

R. Acad. Sci. Paris. 249: 1551-1553<br />

6. GAMAL EL-GHAZALY, ROWLEY J., HESSE M., 1998 - Polarity, aperture condition and germination in pollen<br />

grains of Ephedra (Gnetales). Plant Systematics and Evolution, 213 (3-4): 217-231<br />

7. GRINŢESCU G. P., 1952 - Ephedra L. In: T. SĂVULESCU (red. princip.). Flora României. 1. Bucureşti: Edit.<br />

Aca<strong>de</strong>miei Române<br />

8. JOHRY B. M., BISWAS C., 1997 - The Gymnosperms. Narosa Publishing House, New – Delhi<br />

9. KRÜSSMANN G., 1985 - Manual of cultivated conifers. B.T. Batsford Ltd. London<br />

10. LEHMANN-BAERTS M., 1967 - La morphologie du sporophyte dans le genre Ephedra. La Cellule (Belg.), 67<br />

(5): 7-56<br />

11. MEHRA P. N., 1950 - Inequality in size of the male nuclei in the genus Ephedra. Ann. Bot., July 1950; 14: 331-<br />

339<br />

12. OLTEAN M., NEGREAN G., POPESCU A., ROMAN N., DIHORU G. SANDA V., MIHĂILESCU S., 1994 -<br />

Lista roşie a plantelor superioare din România. Studii, sinteze, documentaţii <strong>de</strong> ecologie, 1<br />

13. PLOAIE G. P., PETRE ZOE. 1979 - Introducere in microscopia electronica cu aplicatii in biologia celulara si<br />

moleculara. Edit. Acad. Romane, Bucuresti<br />

14. SCHNARF K., 1933 - Embryologie <strong>de</strong>r Gymnospermen. In: Linsbauer K. „Handbuch <strong>de</strong>r Pflanzenanatomie”, II<br />

Abt., 2 Teil, Bd. 2. Verlag Gebru<strong>de</strong>r Borntraeger, Berlin<br />

15. SINGH H., 1978. - Embryology of gymnosperms. Berlin-Stuttgart<br />

16. SMARANDACHE D., 2005 - Embriologia plantelor. I. Embriologia arhegoniatelor. Edit. Univ. din Bucureşti,<br />

Bucureşti.<br />

17. STEEVES M. W., BARGHOORN E. S., 1959 - The pollen of Ephedra. J. Arnold Arboretum, 40: 221-255<br />

The explanation of figures:<br />

Plate I<br />

Fig. 1 Ephedra distachya L. - Branch with male cones (1 May 2008; Orig)<br />

Fig. 2 Ephedra distachya L. – Male cone (20 May 2007) (Oc. 10x; Amplific. 2; Orig.)<br />

Fig. 3. Ephedra distachya L. - Longitudinal section of a male cone - fragment (13 April 2008) (Oc 12.5x; ob. 3.2x;<br />

Amplific. 8; Orig.)<br />

Fig. 4. Ephedra distachya L. - Male flower (20 May 2007) (Oc. 10x; Amplific. 3; Orig.)<br />

Fig. 5. Ephedra distachya L. - Longitudinal section through the anther that outlines the archaesporal cells (17 March<br />

2007) (Oc 12.5x.; ob. 25x; Amplific. 160; Orig.)<br />

Fig. 6. Ephedra distachya L. - Cross-section through the male flower (13 April 2008) (Oc. 12.5x; ob. 10x; Amplific.<br />

6.3; Orig.)<br />

Fig. 7. Ephedra distachya L. - Longitudinal section through the male flower (13 April 2008) (Oc. 12.5x; ob. 10x;<br />

Amplific. 6.3; Orig.)<br />

Plate II<br />

Fig. 8 Ephedra distachya L. - Longitudinal section through the male flower (29 May 2001) (Oc. 12.5x; ob. 3.2x;<br />

Amplific.16; Orig.)<br />

Fig. 9. Ephedra distachya L. - Longitudinal section through the anther - anteral wall and young pollen grains (29 May<br />

2001) (Oc. 12.5x; ob. 40x; Ampific. 16; Orig.)<br />

Fig. 10. Ephedra distachya L. - Unicellular pollen grain (17 May 2007) (Oc. 12.5x; ob. 40x; Amplific.16; Orig.)<br />

Fig. 11. SEM micrograph of Ephedra distachya L. poliplicate pollen (21 May 2008; Orig.)<br />

Fig 12. SEM micrograph of Ephedra distachya L. pollen (21 May 2008; Orig.)<br />

27


GENŢIANA PREDAN, IRINA GOSTIN<br />

PLATE I<br />

1 2 3<br />

4 5<br />

6<br />

7<br />

28


GENŢIANA PREDAN, IRINA GOSTIN<br />

PLATE II<br />

8<br />

9<br />

10<br />

11<br />

12<br />

29

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