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Comparative Morphological, Anatomical and Ecological Studies on Two Varieties of Iris unguicularis subsp. carica (Iridaceae) in Turkey

Estudo Comparativo Morfológico, Anatômico e Ecológico de Duas Variedades de Iris unguicularis subsp. carica (Iridaceae) da Turquia

ABSTRACT:

Iris is the largest genus of family Iridaceae having 50 species with 24 endemic to Turkey. Here in this study we compared morphological, anatomical and ecological characters of two varieties of Iris unguicularis subsp. carica (Iris unguicularis subsp. carica var. carica and Iris unguicularis subsp. carica var. syriaca) from Turkey. We reported some distinctive morphological characteristics between both of the varieties like plant size, root length and width, leaf length and width, perianth tube, falls, standard fruit and bract length, falls and standards width and structure, flower colour which are of important taxonomic values. We further investigated that both the varieties are found in different localities and the differences in morphological properties are specific to ecological conditions. Soil analysis of both varieties reveal that CO3, Ca, Mg, Fe and Mn values are more effective than the other soil factors in the distributions of these varieties.

Keywords:
comparison; morphology; anatomy; ecology

RESUMO:

Íris é o maior gênero da família Iridaceae com 50 espécies, sendo 24 endêmicas da Turquia. Neste estudo, comparamos caracteres morfológicos, anatômicos e ecológicos de duas variedades de Iris unguicularis subsp. carica (Iris unguicularis subsp. carica var. carica e Iris unguicularis subsp. carica var. syriaca) da Turquia. Relatamos algumas características morfológicas distintas entre as duas variedades, tamanho da planta, comprimento e largura da raiz, comprimento e largura da folha, diâmetro da tuba, quedas, comprimento padrão da fruta e da bráctea, quedas e padrões de largura e estrutura, cor da flor e importância taxonômica. valores. Nós investigamos ainda que ambas as variedades são encontradas em diferentes localidades e as diferenças nas propriedades morfológicas são específicas das condições ecológicas. Análises do solo de ambas as variedades revelam que os valores de CO3, Ca, Mg, Fe e Mn são mais efetivos que os demais fatores do solo nas distribuições dessas variedades.

Palavras-chave:
comparação; morfologia; anatomia; ecologia

INTRODUCTION

Family Iridaceae has about 85 genera in which Iris L. is the largest genus. There are 56 taxa of this genus distributed in Turkey (50 species, 3 subspecies, and three varities) with 24 endemics (Mathew, 2001Mathew B. Some aspects of the Juno group of irises. Proceedings of the International Iridaceae conference. Special Volume. Ann Bot. 2001;1:113-22.; Güner et al., 2012Güner A. Iris L. in Turkey Plants List (Vascular Plants). Istanbul: Nezahat Gökyigit Botanical Garden and Flora Research Association Publication; 2012. p.535-40.). The genus contains bearded, crested and beardless species. The under-ground parts of the genus are mostly rhizomatic, bulb and tuber shaped. Iris taxa are economically important geophytes producing different secondary metabolities. The Iris L. species are used to treat many diseases for a long time as anti-flammatory, diuretic, analgesic, wound-healing agents, anti-bacterial, anti-viral, and anti-cancer (Wollenweber et al., 2003Wollenweber E, Stevens JF, Klimo K, Kanauft J, Norbert F, Clarissa G. Cancer chemopreventive in vitro activities of isoflavones isolated from Iris germanica. Planta Med. 2003;69:15-20.; Kukula-Koch et al., 2013Kukula-Koch W, Sieniawska E, Widelski J, Urjin O, G³owniak P, Skalicka-WoŸniak K. Major secondary metabolites ofIrisspp. Phytochem Rev. 2013;14(1):51-80. ). Their rhizomes are also used to treat inflammation of the upper respiratory tract, gastrointestinal tract, in gynecology and oncology practices (Williams, 1997Williams CA. Flavonoid and xanthone patterns in bearded Iris species and the pathway of chemical evolution in the genus. Biochem Syst Ecol. 1997;25:309-25.; Iwashina et al., 1998Iwashina T, Tsukasa I, Ootani S. Flavonoids of the genus Iris; structures, distribution and function. Rev Ann Tsukuba Bot Gard. 1998;17:147-83.). Iris unguicularis from the same genus is known for its medicinal properties because its rhizomes contains 1,3-O-diferuloylsucrose, 5,7-dihydroxy-6-methoxychromone, irilone, 4,5,7-trihydroxy-methoxyflavanone, tectorigenin, kaempferol, 4,5,7-trihydroxy-3,8-dimethoxyflavanone, 8-methoxyeriodictyol, hispidulin, mangiferin, irigenin and kanzakiflavones-1 (Arisawa and Morita, 1976Arisawa M, Morita N. Studies on constituents of genus Iris. VII The constituents of I. unguicularis Poir. Chem Pharm Bull. 1976;24:815-7. ; Rahman et al., 2010Rahman A, Hareem S, Choudhary MI, Sener B, Abbaskhan A, Siddiqui H, et al. New and known constituents from Iris unguicularis and their antioxidant activity, Heterocycles. 2010;82:813-24. ; Mosihuzzmana et al., 2013Mosihuzzman M, Naheed S, Hareem S, Talib S, Abbas G, Khan SN, et al. Studies on á- glucosidase inhibition and anti-glycation potential of I. loczyi and I. unguicularis. Life Sci. 2013;92:187-92.). Besides these uses their rhizomes is also are used in making “cheese curd” (Baser, 1997Baser KHC. Current knowledge on the wild food and non-food plants of Turkey. Cah Options Med. 1997;3:129-59. ). Sofiane et al., (2016Sofiane G, Wafa N, Loubna A. Evalution of antioxidant and antifungal activities of methanolic aerial part extract of I. unguicularis Poiret. Asian J Plant Sci Res. 2016;6(4):18-23 ) reported that the above-ground parts of I. unguicularis have high antioxidant and antifungal properties too.

The genus Iris is divided into six subgenera recognized within subgenus Limniris include beardless irises and widely distributed in the Northern Hemisphere. This subgenus contains sections Limniris and Lophiris. The section Limniris is divided into sixteen series within the series Unguiculares (Stebbings, 1997Stebbings G. The Gardener’s guide to growing irises. Newton Abbot: David and Charles; 1997. p.16-8. ). Both Limniris and Lophiris sections are reported to be polyphyletic (Wilson, 2004Wilson CA. Phylogeny of Iris based on chloroplast matK gene and trnK intron sequence data. Mol Phylog Evol. 2004;33:402-12.). Unguiculares (Diels) Lawrence series is a small group and plants of this series are with problematic taxonomy (Davis and Jury, 1990Davis AP, Jury SL. A taxonomic review of IrisL. series Unguiculares (Diels) Lawrence. Bot J Linn. Soc. 1990;103:281-300.). Iris unguicularis belongs to series Unguiculares of Limniris subgenus and is widely cultivated in temperate regions. It is a perennial rhizomatous flowering plant in the genus Iris, their species blossom in late winter and early spring with pleasant fragrance, large in size, light lavender blue coloured and delicate. The leaves are bright green coloured, erect, slender, linear, striped and 10-60 cm at the time of anthesis. Morphologically, this species is very similar to I. lazica Aldov. However, leaf width of I. unguicularis is smaller than leaf width of I. lazica. Leaves width, pollen morphology, and leaf chemical components are the most important distinguishing characters between these two species (Davis and Jury, 1990). In addition, I. laziza does not like very hot dry areas, and prefers relatively damp areas with Blacksea element. Similary, I. unguicularis is known as bush navruz by people and represented with a subspecies in Turkey, named subsp. carica. Based on differeces in the leaf width measurements, I. unguicularis subsp. carica was divided into two varieties as var. carica and var. syriaca. Iris unguicularis subsp. carica (Wern. Schulze) A.P.Davis & Jury var. carica, has a leaf width 1-2 mm, while leaf width of I. unguicularis subsp. carica var. syriaca (Wern. Schulze) A.P. Davis & Jury is 2-5 mm. The var. carica is endemic to East Mediterranean region of Turkey, whereas the var. syriaca is found in East Mediterranean region but not endemic (Güner et al., 2000Güner A, Özhatay N, Ekim T, Baser KHC. Flora of Turkey and the East Aegean Islands. Edinburg: University Press; 2000. p.270-1., 2012). Var. carica disributes in the Mediterranean and Agean coasts from 1-1500 m. and blossom between January to June while var. syriaca from 600-1000 m. blossom in February-April. Here in this investigation we compared morphological, anatomical and ecological characters of I. unguicularis subsp. carica var. carica and I. unguicularis subsp. carica var. syriaca varieties to report the significant distinguishing characters in term of taxonomy.

MATERIAL AND METHODS

The materials of I. unguicularis subsp. carica var. carica and I. unguicularis subsp. carica var. syriaca were collected during the flowering period between 2016 and 2017. The localities of plant samples are listed below.

Iris unguicularis subsp. carica var. carica

1. C2 Mugla: Fethiye to Ölüdeniz road, under Pinus brutia forest, 250 m., 3 March 2017, Çelik 644 (A1 locality)

2. C2 Mugla: Fethiye to Dalaman, 4 km. to Göycek Passage, under Pinus brutia forest, 160 m., 3 March 2017, Çelik 645 (A2 locality).

3. C2 Mugla: Yaraþ behind the water fountain, under Pinus brutia forest, 720 m., 3 March 2017, Çelik 646 (A3 locality).

4. C2 Mugla: Yilanli mountain, Yaras Village, Pinus brutia forests, 1000 m., 7 March 2016, Çelik, 642 (A4 locality).

Iris unguicularis subsp. carica var. syriaca

5. C6 Hatay: Saman Mountain, Tekepinari Gömbece Village, Pinus brutia forest and mixed shrubs, 600 m., 5 March 2017, Çelik, 647 (B1 locality).

6. C6 Osmaniye: Kadirli, Tahta Village, Cincikli location, rare scrub areas, 900 m., 21 March 2016, Çelik, 643 (B2 locality).

Both varieties were identified according to Güner et al. (2000Güner A, Özhatay N, Ekim T, Baser KHC. Flora of Turkey and the East Aegean Islands. Edinburg: University Press; 2000. p.270-1., 2012). The plant samples were fixed in 70% alcohol and then used for morphological measurements. Paraffin method was used (Algan, 1981Algan G. Microtechnic for plant tissues. Istambul: Firat University Press; 1981.) to prepare cross-sections of the roots, scapes and leaves. The cross and surface-sections of these parts were taken and photographed. The cross-sections were stained with sartur reagent. The anatomical and morphological measurements were made with a micrometric ocular and ruler. The distinguishing morphological and anatomical characters were given in Table 1 and3, respectively. Mean epidermal and stoma cells numbers in 1 mm2 of the surface-section were determined. Length and width of stomata in the lower surfaces of leaves were measured (Table 2). Stomatal index was calculated according to the description of Mesdner and Mansfield (1968Mesdner H, Mansfield TA. Physiolgy of stomata. London: McGraw-Hill; 1968.). For soil analysis samples were taken from 0-20 cm depth during generative growth period and were brought in polyethylene bags to the laboratory. Physical and chemical analyzes of the soil samples, were carried out in Amasya University Central Research Application Laboratory Application and Research Center. The soil texture, total salinity, calcium carbonate (CaCO3) and pH were determined according to the standard methods (Kaçar, 1996Kaçar B. Chemical analysis of plant and soil. Ankara: Foundation of Education; Research and Development Publication; 1996.). Nitrogen, phosphorus, potassium, organic matter and microelements contents of the soil samples were analyzed by micro-Kjeldahl apparatus, ammonium-molybdate-stannous chloride, flame photometer, the Walkley-Black, DTPA (Diethylenetriaminepentaacetic acid) + CaCl2 (Calcium chloride) + TEAL (Triethanolomine) methods, respectively (Kaçar, 1996).

Table 1
Distinguishing morphological characters of investigated varieties

Table 2
Stomata measurements and stomata index for varieties (lower surface of leaf)

Table 3
Distinguishing anatomical characters of investigated varieties (all dimensions are µm)

RESULTS AND DISCUSSION

Morphological characteristics

Iris unguicularis subsp. carica var. carica: Plants are perennial herbs, 12-40 cm in height, and rhizomatous. Their rhizomes are thick, pale-brown with membranous sheaths. Roots are tough, thin and intensive, 18-30 cm x 1-1.5 mm in length. Leaves are linear, slender, flat, erect, striped, bright green, longer than the scape and 10-60 x 1-2 mm at anthesis, pointed, forming dense clumps (Figure 1A). Scapes are erect, selender, sheathed, unbranched and 1-2 flowered. Bract and bracteoles 7-25 cm, linear-lanceolate and short sipicular. Perianth tube wrapped with bract and bracteoles, long-tapering at apex, 8-25 cm. Flowers are solitary, pretty dark lavender-blue to deep lilac, with delicate marking and sweetly-scent. Falls oblanceolate, 5.5-7.4 x1-1.7 cm, acute, recurved, pale violet, with narrow long-tapering claw, white veined, with a strong deep yellow median stripe on falls. Claws yellowish, veined with red-purple, oblong spathulate, subequal and entire. Standards oblanceolate, 6-7.5 x 1.4-1.7 cm., acute, rounded at the top, pale violet coloured and erect. The base of standards and falls burgundy coloured. Stylar tube 1.5-2 cm, style branches 2.5-3 x 0.3-0.4 cm, with acute lobes 1-1.2 x 0.2 cm. Crest is 2-4 mm. Ovary narrow, selender and 9-12 x 2-4 mm. Stamens lilac coloured. Capsule ellipsoid, 3-4 x 1-1.5 cm, carried on a short peduncle. Found along dry sunny banks, edges of scrub, open pine woodlands and rocky places, 1-1500 m.

Figure 1
General appearances of herbarium samples of varieties. A, var. carica; B, var. syriaca, r,root; rh, rhizome; s, scape; l, leaf; f, flower.

Iris unguicularis subsp. carica var. syriaca: Plants are perennial herbs, 20-55 cm in height, and rhizomatous. Thier rhizome is thick, pale-brown with membranous sheaths. Roots are tough, thin and intensive, 14-25 cm x 1-1.8 mm. Leaves are linear, slender, flat, erect, striped, bright green, longer than the scape and 10-50 x 2-5 mm at anthesis, pointed, forming dense clumps (Figures 1B). Scapes are erect, selender, sheathed, unbranched and 1-2 flowered. Bract and bracteoles 12-20 cm, linear-lanceolate and short spicular. Perianth tube wrapped with bract and bracteoles. Perianth tube long-tapering at apex, 13-20 cm. Flowers solitary, pretty light lavender-blue to deep lilac, with delicate marking and sweetly-scented. Falls oblanceolate to lanceolate-rhombic, 5.5-7.9 x 1-1.9 cm, acute, recurved, pale violet, with narrow long-tapering claw, white veined, with a strong deep yellow median stripe on falls. Claws yellowish, veined with red-purple, oblong spathulate, subequal and entire. Standards oblanceolate-lanceolate-rhombic, 6.5-8.2 x 1.2-2.1 cm, acute, rounded at the top, pale violet coloured and erect. The base of standards and falls burgundy coloured. Stylar tube 1.5-2 cm and style branches 2.5-3 x 0.3-0.4 cm, with acute lobes 1-1.2 x 0.2 cm. Crest 2-4 mm. Ovary narrow, selender and 9-12 x 2-4 mm. Stamens lilac coloured. Capsule ellipsoid, 2.5-4 x 1-1.5 cm, carried on a short peduncle. Found near bushes and in meadow places, withing Pinus brutia forest 600-1000 m.

Anatomical characteristcs of the roots

Iris unguicularis subsp. carica var. carica: Epidermis is single layered, large celled with simple, multi-celled and dense eglandular trichomes. Cortex is multilayered (10-15 layered) and parenchymatic (Figure 2A). The parenchyma cells are oval and cylindrical shaped with undulated margins. Cortex cells near the endoderm, are small and oval shaped with no idioblasts. Endodermis is single layered and with large parenchymatic cells. The thickening in endodermis cells are three sided and oriented to pericycle. There is no thickening towards cortex. The thickening in endodermis cells are very obvious (Figure 2B). Pericycle is 1-3 layered with large and oval parenchymatic cells. Pericycle cells are smaller than endodermis cells. Xylem is 12-15 strands. There are large and oval shaped parenchyma cells in the pith.

Figure 2
The root cross-sections of varieties. A, B, var. carica; C, D, var. syriaca, e, epiderma; ex, exoderma; p, parenchyma; en, endoderma; pr, pericycle; ph, phloem; t, trachea, pt, pith; eg, eglandular trichomes

Iris unguicularis subsp. carica var. syriaca: In root cross-section, epidermis is single layered, with large cells and dense eglandular trichomes. Cortex parenchyma is 12-16 layered. Parenchyma cells are very large, oval and cylindrical shaped (Figure 2C). The margins of these cells are not undulated, but straight. In the cortex, idioblasts are observed. Endoderm is single layered and parenchymatic. Endodermis cells are large. The thickening in endodermal cells are three sided, very evident and oriented to pericyle. There is no thickening towards cortex. Pericycle occurs from large, oval shaped and 1-2 layered parenchymatic cells. Endodermis cells are larger than pericycle cells. Xylem has 12-16 strands. In the pith region, there are large, oval and hexagonal shaped parenchyma cells (Figure 2D).

Anatomical characteristcs of the scapes

Iris unguicularis subsp. carica var. carica: Cuticle is thin. Epidermis is single layered, large and square shaped. Papillae and micropapillae are seen over the epidermis and cuticle, respectively. There is lacunal collenchyma under epidermis which is 1-3 layered. Cortex contains either oval or circular shaped and large or small parenchyma cells (Figure 3A). Parenchymatic cells are multilayered. Parenchyma cells in the cortex and pith are filled with dense granule-like matters or idioblasts and rare styloids. Large and small vascular bundles are located disorderly in cortex and central cylinder. The xylem and phloem elements are apparent in the vascular bundles (Figure 3B). Xylem elements are in arch-shaped. There are sclerenchyma cells at the phloem pole of vascular bundles. Bundle sheath is not obvious. The pith consists of large, thin walled and rounded shaped parenchymatic cells.

Figure 3
The scape cross-sections ofvarieties. A, B, var. carica; C, D,var. syriaca, c, cuticle; e. epiderma; cl, collenchyma; p, parenchyma; sc, styloids; cr, crystalline granules; ph, phloem; x; xylem, t, trachea; id, idioblasts

Iris unguicularis subsp. carica var. syriaca: Epidermis is single layered, large and square shaped. The cuticle is thin in the cross-section of scape. Lacunal collenchyma is 3-5 layered. The papillae and micropapillae are seen over the epidermis and cuticle, respectively. Cortex is composed of oval or circular shaped and large parenchyma cells (Figure 3C). The cortex is 10-13 layered. There are dense granule-like matters or idioblasts in the cortex parenchyma cells. Vascular bundles are disordered. In the cross-section of scape, there are large and small vascular bundles (Figure 3D). In the phloem pole of vascular bundles have dense sclerenchyma. Bundle sheath consists of one layered, and thin walled parenchymatatic cells. The parenchyma cells in the pith are large and rounded.

Anatomical characteristcs of the leaves

Iris unguicularis subsp. carica var. carica: Leaf is isobilateral ensiform type. Cuticle is very thick in both lower and upper epidermises. Both epidermises cells are single layered, large celled and square shaped. Epidermis cells and cuticle layer include papillae and dense micropapillae, respectively. Micropapillae on the cuticle layer are extremely conspicuous. Palisade-like parenchyma is 1-2 layered and small-cylindrical shaped. Spongy-like parenchyma is 3-5 layered. The mesophyll cells in the center are large, circular shaped and without chlroplast. There are large cavities in the mesophyll. Vascular bundles are in single row on each side of the leaf (Figure 4A). Large vascular bundles are at margin (large marginal bundles) and keel base (large keel bundles). Small vascular bundles present in the mesophyll regions between two large keel bundles. There is a large marginal vascular bundle at the corner of leaves. Xylem of vascular bundles is directed towards the leaf center. Phloem of vascular bundles is directed towards the lower and upper epidermises. The phloem and xylem elements are observed clearly. The bundle sheath is clear. There are marginal sclerenchyma cap only at phloem pole of large and small vascular bundles and at the leaf margin (Figure 4B). The sclerenchma cap is V-form and extends towards epidermis. In the xylem pole has large oval shaped parenchymatic cells without chloroplast. Stomata are rather below the epidermis cells. Each stoma is large, dense and ordered (Figure 5A). In mesophyll and both epidermises, crystalline granules are dense. But, styloids are rare in mesophyll. The keels in both epidermises are more clearer and little rounded. The leaf parts in the regions between keels are narrow, and keels in the epidermis are dense.

Figure 4
The leaf cross-sections of varieties. A, B, var. carica; C, D,var. syriaca, c, cuticle; ue, upper epiderma; pp, palisade parenchyma; sp, spongy parenchyma, vb, vascular bundles; sb, sheath bundle; sk, sclerenchyma; le, lower epiderma; mp, micropapillae; cv, cavities.

Figure 5
The leaf surface-sections of varieties. A, var. carica; B,var. syriaca, ec, epidermis cell; cr, crystalline granules; st, stoma cell; sc, styloids.

Iris unguicularis subsp. carica var. syriaca: Leaf is in isobilateral type (Figure 4C). Upper and lower epidermises cells are square shaped, large, single layered and with papillae. Cuticle layer is thick and conspicuous micropapillae. The side walls of upper and lower epidermises cells are undulated. Bulliform cells are rare. Stomata are frequent in both epidermises and are of amaryllis type (Figure 5B). Stomata are rather below the epidermis cells (xeoromorphic structure). Mesophyll contains rounded or radially elongated parenchyma cells. There is palisade-like parenchyma in the outermost layer and is 1-2 layered in the upper and lower epidermises. These cells are with dense chloroplast. The spongy-like parenchyma in the innermost is 4-5 layered, oval shaped and with less chloroplast. The large cavities and large parenchyma cells are in the centre of mesophyll (Figure 4D). Crystalline granules and styloids are less in number in the mesophyll. However, crystalline granules are dense in the epidermis cells. Vascular bundles are located as two circles and in pairs opposite to each other. Large vascular bundles are at margin (large marginal bundles) and keel base (large keel bundles). Small vascular bundles are present in the mesophyll regions between two large keel bundles. Phloem and xylem elements are obvious. Vascular bundles contain bundle sheath, which has one layered and thin walled parenchymatous cells without chloroplast. There are dense sclerenchyma cap at phloem pole and at the leaf margin. The sclerenchma cap is V-form and almost adjacent to epidermis. There are parenchyma cells, which are large, oval shaped and without chloroplast, at xylem pole of vascular bundles. The keels in the lower and upper epidermises are less obvious and little rounded.

Physical and chemical characters of the soil samples

Iris unguicularis subsp. carica var. carica: It is an endemic to Turkey with limited distribution and vulnerable. Its soil characteristics are based on four localities (A1, A2, A3 and A4) in Mugla. The salinity contents of the soil samples were 536-616 ms cm-1. The pH and CaCO3 values were 6.65-6.93 and 0.071-0.078% respectively. The soil samples had loamy and loamy-sandy texture (Table 4). While the N and organic matter contents were between 2.76-2.82% and 4.54-4.65% respectively, the P and K contents were between 1.36-1.46 kg da-1 and 45.126-45.379 kg da-1 respectively. The Ca, Mg and Cu contents of soil samples ranged between 3220-3228, 254.1-254.9 and 0.629-0.640 ppm in order, while the Zn, Mn, Na and Fe contents of soil samples ranged between 0.748-0.753, 4.201-4.208, 19.499-19.521 and 25.48-25.54 ppm, respectively.

Table 4
Physical and chemical properties of soil samples (A: I. unguicularis subsp. carica var. carica, B: I. unguicularis subsp. carica var. syriaca)

Iris unguicularis subsp. carica var. syriaca: It is not an endemic species to Turkey but has limited distribution in Turkey. Soils samples were taken from 2 different localities (B1 and B2) in Hatay and Osmaniye. The soil samples in B1 and B2 localities have sandy texture structure. The pH values varied from 6.99 to 7.69. The total salinity of soil samples was between 320 and 390 µs cm-1. The level of CaCO3 concentration was 52.60-59.12%. The organic matter, N, P and K values of soils ranged between 2.51-3.45%, 1.30-2.70%, 1.15-1.50 kg da-1 and 32.56-35.99 kg da-1, respectively (Table 4). The Zn, Mn, Na and Fe values were 0.317-0.738, 0.708-0.935, 19.87-21.21 and 1.781-2.078 ppm, while the Ca, Mg and Cu values were 67.90-7902, 346.2-370.9 and 0.480-0.601 ppm, respectively.

The taxon I. unguicularis subsp. carica has been divided into two varietiesi.e. I. unguicularis subsp. carica var. carica and I. unguicularis subsp. carica var. syriaca (Güner et al., 2000Güner A, Özhatay N, Ekim T, Baser KHC. Flora of Turkey and the East Aegean Islands. Edinburg: University Press; 2000. p.270-1., 2012) based on the leaf width measurements. Here in this study, we observed some other distinctive morphological characters between both varieties like; plant size, root length and width, leaf length and width, perianth tube, fall, standard, fruit and bract length, fall and standard width and structure, flower colour. These morphological characters are of important taxonomic values, between both the varieties (Table 1). Other morphological characters were very similar in the investigated two varieties. We further observed that both the varieties are found in different localities in Turkey and reveal that differences in morphological properties of the same species collected in different localities are specific to ecological conditions.

In root and leaf anatomical characters of the two varieties, some different characters such as; length and width of epidermis and cortex cells, diameter of pith cells, length of endodermis cells, the layer number of cortex, margin structure of cortex cells, number of xylem strands, layer number of pericycle, density and size of stomata, density of crystal granules, length and width of palisade-like parenchyma cells, status of keels, thickness of cuticle, diameter of trachea, whether the side walls of the upper and lower epidermises cells are undulated, presence and absence of bulliform cells and density of micropapillae are observed (Tables 2and3). The above situation was also found in root and leaf anatomical characters of some Iris taxa by Kandemir and Çelik (2017Kandemir N, Çelik A. Comparison of morphological and anatomical properties of endangered endemic Iris pamphylica and I. masia in Turkey. Acta Bot Hung. 2017;59:371-88.). In the cross-sections of leaf, the keels in the lower and upper epidermises of var. syriaca were less obvious. However, the keels in both epidermises of var. carica were clearer. We think that these characters may be used as distinguished taxonomic characters in the classification of these varieties. Nikolic and Mitic (1991Nikolic T, Mitic B. Phenetic relationships within populationsof Iris illyrica, I. palliida and I. peudopallida (Iridaceae) with regard to morphological characteristics of epidermis. Acta Bot Croat. 1991;50:99-106.) pointed out that leaf anatomical characters could also be a significant diagnostic charaters for some Iris species. Similarly, Rudall (1994Rudall P. Anatomy and systematics of Iridaceae. Bot J Linn Soc. 1994;114:1-21.) reported that leaf anatomical characters are significant for classification of the family. On the other hand, the quantity and shape of sclerenchyma cap (V-form) in the vascular bundles are very interesting in the taxa of Limniris subgenus. This type of sclerenchyma was obtained in the leaf of Iris pseudacorus L. by Gontova and Zatylnikova (2013Gontova TN, Zatylnikova OA. Comparative morphologival and anatomical study of leaves and stem of Iris Pseudocorus and Iris Sibirica. Int J Biol Pharm Allied Sci. 2013;5(3):574-8. ). Rudall (1991Rudall P. Leaf anatomy in Tigridieae (Iridaceae). Plant Systematics and Evolution. 1991;175:1-10.) reported that the amount of sclerenchyma varied among species. We think that shape of sclerenchyma cap and presence of keel in both epidermises are of taxonomic value among subgenera of Iris genus. So, taxa belonging to Limniris subgenus may be easily distiguished from other taxa of Iris genus. The similar status was found in the vascular bundles of I. pseudacorus and I. sibirica leaves by Gontova and Zatylnikova (2013). Although some distinguishing anatomical characters e.g., diameter of epidermis cells, layer number of lacunal collenchyma and whether the bundle sheath was obvious are identified in the scapes of investigated varieties, but most characteristics are similar in the scape of both varieties.

Xeoromorphic leaf characters like stomata below the epidermal cells, mesophyll in isobilateral structure, vascular bundles with dense sclerenchyma are observed. Sclerenchyma are also found on the margin of the leaf, extending to the epidermis as girders. The xeoromorphic leaf characters are also found in other taxa of Iridaceae (Rudall and Mathew, 1990Rudall P, Mathew B. Leaf anatomy in Crocus (Iridaceae). Kew Bull. 1990;45:535-44.; Rudall, 1991; Kandemir, 2015Kandemir N. Leaf anatomical properties of some rare and endemic Iris L. taxa and their reletions: Subgenus Hermodactyloides in Turkey. Iran J Bot. 2015;21:142-51. ; Kandemir and Yakupoglu, 2016Kandemir N, Yakupoglu H. Morphological and anatomical properties od endemic Iris nezahatiae distributed in the North-East Anatolia region (Turkey). BEU Journal of Science. 2016; 5(1):104-12. ). Mitic and Liber., (2000Mitic BNT, Liber Z. Morphological and anatomical in Alpine-Dinaric populations of the genus Iris L. Pallidae Series (A. Kern.) Trinajstic (Iridaceae). Acta Soc Bot Pol. 2000;69(4):285-91.) reported that the anatomical characters are closely related to the climatic conditions, especially the xeromorphic or mesomorphic aspect of the habitate.

In leaves of both varieties, V-form sclerenchyma cap extends to the epidermis, a character found in some species of Tigridieae (Iridaceae) and Iridaceae by Rudall (1991Rudall P, Goldblatt P. Leaf anatomy and phylogeny of Ixioideae (Iridaceae). Bot J Linn Soc. 1991:106:329-45., 1994). However the sclerenchyma cap does not extend to epidermis in some taxa of Iridaceae. Since leaf margin structures are different in the taxa of Iridaceae, these characters are reported to be significant in generic groupings of Iridaceae taxa by Rudall and Goldblatt (1991). In these varieties, dense both marginal sclerenchyma and subepidermal marginal sclerenchyma are found on the margins and the corner of leaves, respectively. Leaves margin structures of both varieties are similar, but this character can be used to distinguish genera and subgenera of Iridaceae. Styloids and idioblasts in different shapes were seen in Iris taxa by Rudall (1994). Wu and Cutler (1985Wu QG, Cutler DF. Taxonomic, evolutionary and ecological implications of the leaf anatomy of rhizomatous Iris species. Bot J Linn Soc. 1985;90:253-303.) emphasized that variations in styloids size and shape are significant among Iris taxa. However, similar idioblast, crystal granules and styoloids are seen in the root, scape and leaf of both varieties. Therefore, these charactres are not important in distinguishing of the two varieties.

Soil analysis revealed that I. unguicularis subsp. carica var. carica prefers slightly saline, loamy-sandy and loamy soils, while I. unguicularis subsp. carica var. syriaca disrtibutes in saltless and sandy soils. It was found that some Iris, Crocus L. and Scilla L. taxa (Kandemir et al., 2011Kandemir N, Çelik A, Sürücü A. Ecological response of some Iris L. taxa (Iridaceae) in Turkey. Bangladesh J Bot. 2011;40:177-84., 2012; Kandemir, 2016Kandemir N. Top senescence in the endemic Iris nezahatiae, critically endangered, and distributed in the North-East Anatolia Region (Turkey). Ecology. 2016;25:1-8.; Kandemir et al., 2018Kandemir N, Çelik A, Yayla F. Ecological properties and close relationships of some Scilla L. taxa (Asparagaceae) in Turkey. Int J Agric Biol. 2018;20:307-14.) prefer loamy and loamy-sandy soils because the drainage of these types of soils is good. The var. syriaca grows usually in slightly alkaline and neutral soils, while var. carica grows in neutral soils. It is shown in Table 4 that var. carica grows at low calcareous soils and var. syriaca grows at high calcareous level soils. The same states are found in some Crocus and Iris taxa by Kandemir et al., (2011Kandemir N, Çelik A, Sürücü A. Ecological response of some Iris L. taxa (Iridaceae) in Turkey. Bangladesh J Bot. 2011;40:177-84., 2012Kandemir N, Çelik A, Yayla F. Comparative anatomic and ecologic investigation on some endemic Crocus taxa (Iridaceae) in Turkey. Pak J Bot. 2012;44:1065-74.) and Kandemir (2016Kandemir N. Top senescence in the endemic Iris nezahatiae, critically endangered, and distributed in the North-East Anatolia Region (Turkey). Ecology. 2016;25:1-8.). The investigated taxa prefer rich organic matter and nitrogen soils. It was reported that some Iris taxa (Kandemir et al., 2011) grow in soils with rich levels of organic matter and nitrogen. However, soil P contents of both the varieties are found to be at deficiency levels. This state may occur, since P is rather phloem-immobile ion and stored in the form of insoluble form (calcium-phosphate) in soil. And, also in alkaline soils, pH affects the nutrient element intake of plants. In such soils, CaCO3 contents increase and this increase cause low P contents (Özdemir and Öztürk, 1996Özdemir F, Öztürk M. Studies on the autecology of Capparis L. species distributed in West Anatolia. Turk J Bot. 1996;20:117-25.). Therefore, plants cannot get any benefit from P. K, Ca, Cu, Mg, Mn, Fe and Zn contents of the varieties are in sufficient amount in all soil samples. It was reported that K, Cu, Mg, Mn, Fe, Zn and contents of soils where some Iris and Crocus taxa grow are generally enough (Kandemir et al., 2011, 2012). K is very phloem-mobile ion. Sodium (Na) contents of both varieties are low in all localities. While CO3, Ca and Mg contents are high in the var. syriaca, Fe and Mn contents are high in the var. carica. The difference has seen among CO3, Ca, Mg Fe and Mn contents of var. syriaca and var. carica, but there is no other difference between other ecological properties. Therefore, var. syriaca and var. carica are close ecological taxa. On the other hand, minor differences in some ecological characters are observed. The reason of differences in these ecological characters may be due to their exposure to various ecological and climatic factors in the distribution areas of these Iris taxa.

In conclusion distinguishing morphological and anatomical characters to taxanomic values are determined in both varieties. Additionally, some similar morphological, anatomical and ecological characters were found in these varieties. Specially, both the varieties can be distinguished by the root, scape and leaf anatomical characters. As a result, we suggest that these two varieties should be promoted to subspecies category related to the differences in morphological, anatomical and ecological characteristics. In order to confirm the data, it is required to get more detailed studies on both varieties. Although there is plenty of knowledge in the literature, it is reported that this knowledge is not sufficient to figure out the relationships between sections in the subgenera of Iris genus (Wilson, 2011Wilson CA. Subgeneric classification in Iris re-examined using chloroplast sequence data. Taxon. 2011;60:27-35. ; Guo and Wilson, 2013Guo J, Wilson AC. Moleculer phylogeny of crested Iris based on five plastid markers (Iridaceae). Syst Bot. 2013;38:987-95. ).

REFERENCES

  • Algan G. Microtechnic for plant tissues. Istambul: Firat University Press; 1981.
  • Arisawa M, Morita N. Studies on constituents of genus Iris VII The constituents of I. unguicularis Poir. Chem Pharm Bull. 1976;24:815-7.
  • Baser KHC. Current knowledge on the wild food and non-food plants of Turkey. Cah Options Med. 1997;3:129-59.
  • Davis AP, Jury SL. A taxonomic review of IrisL. series Unguiculares (Diels) Lawrence. Bot J Linn. Soc. 1990;103:281-300.
  • Gontova TN, Zatylnikova OA. Comparative morphologival and anatomical study of leaves and stem of Iris Pseudocorus and Iris Sibirica Int J Biol Pharm Allied Sci. 2013;5(3):574-8.
  • Guo J, Wilson AC. Moleculer phylogeny of crested Iris based on five plastid markers (Iridaceae). Syst Bot. 2013;38:987-95.
  • Güner A, Özhatay N, Ekim T, Baser KHC. Flora of Turkey and the East Aegean Islands. Edinburg: University Press; 2000. p.270-1.
  • Güner A. Iris L. in Turkey Plants List (Vascular Plants) Istanbul: Nezahat Gökyigit Botanical Garden and Flora Research Association Publication; 2012. p.535-40.
  • Iwashina T, Tsukasa I, Ootani S. Flavonoids of the genus Iris; structures, distribution and function. Rev Ann Tsukuba Bot Gard. 1998;17:147-83.
  • Kaçar B. Chemical analysis of plant and soil. Ankara: Foundation of Education; Research and Development Publication; 1996.
  • Kandemir N, Çelik A, Sürücü A. Ecological response of some Iris L. taxa (Iridaceae) in Turkey. Bangladesh J Bot. 2011;40:177-84.
  • Kandemir N, Çelik A, Yayla F. Comparative anatomic and ecologic investigation on some endemic Crocus taxa (Iridaceae) in Turkey. Pak J Bot. 2012;44:1065-74.
  • Kandemir N. Leaf anatomical properties of some rare and endemic Iris L. taxa and their reletions: Subgenus Hermodactyloides in Turkey. Iran J Bot. 2015;21:142-51.
  • Kandemir N, Yakupoglu H. Morphological and anatomical properties od endemic Iris nezahatiae distributed in the North-East Anatolia region (Turkey). BEU Journal of Science. 2016; 5(1):104-12.
  • Kandemir N. Top senescence in the endemic Iris nezahatiae, critically endangered, and distributed in the North-East Anatolia Region (Turkey). Ecology. 2016;25:1-8.
  • Kandemir N, Çelik A. Comparison of morphological and anatomical properties of endangered endemic Iris pamphylica and I. masia in Turkey. Acta Bot Hung. 2017;59:371-88.
  • Kandemir N, Çelik A, Yayla F. Ecological properties and close relationships of some Scilla L. taxa (Asparagaceae) in Turkey. Int J Agric Biol. 2018;20:307-14.
  • Kukula-Koch W, Sieniawska E, Widelski J, Urjin O, G³owniak P, Skalicka-WoŸniak K. Major secondary metabolites ofIrisspp. Phytochem Rev. 2013;14(1):51-80.
  • Mathew B. Some aspects of the Juno group of irises. Proceedings of the International Iridaceae conference. Special Volume. Ann Bot. 2001;1:113-22.
  • Mesdner H, Mansfield TA. Physiolgy of stomata. London: McGraw-Hill; 1968.
  • Mitic BNT, Liber Z. Morphological and anatomical in Alpine-Dinaric populations of the genus Iris L. Pallidae Series (A. Kern.) Trinajstic (Iridaceae). Acta Soc Bot Pol. 2000;69(4):285-91.
  • Mosihuzzman M, Naheed S, Hareem S, Talib S, Abbas G, Khan SN, et al. Studies on á- glucosidase inhibition and anti-glycation potential of I. loczyi and I. unguicularis Life Sci. 2013;92:187-92.
  • Nikolic T, Mitic B. Phenetic relationships within populationsof Iris illyrica, I. palliida and I. peudopallida (Iridaceae) with regard to morphological characteristics of epidermis. Acta Bot Croat. 1991;50:99-106.
  • Özdemir F, Öztürk M. Studies on the autecology of Capparis L. species distributed in West Anatolia. Turk J Bot. 1996;20:117-25.
  • Rahman A, Hareem S, Choudhary MI, Sener B, Abbaskhan A, Siddiqui H, et al. New and known constituents from Iris unguicularis and their antioxidant activity, Heterocycles. 2010;82:813-24.
  • Rudall P. Leaf anatomy in Tigridieae (Iridaceae). Plant Systematics and Evolution. 1991;175:1-10.
  • Rudall P, Goldblatt P. Leaf anatomy and phylogeny of Ixioideae (Iridaceae). Bot J Linn Soc. 1991:106:329-45.
  • Rudall P, Mathew B. Leaf anatomy in Crocus (Iridaceae). Kew Bull. 1990;45:535-44.
  • Rudall P. Anatomy and systematics of Iridaceae. Bot J Linn Soc. 1994;114:1-21.
  • Sofiane G, Wafa N, Loubna A. Evalution of antioxidant and antifungal activities of methanolic aerial part extract of I. unguicularis Poiret. Asian J Plant Sci Res. 2016;6(4):18-23
  • Stebbings G. The Gardener’s guide to growing irises. Newton Abbot: David and Charles; 1997. p.16-8.
  • Williams CA. Flavonoid and xanthone patterns in bearded Iris species and the pathway of chemical evolution in the genus. Biochem Syst Ecol. 1997;25:309-25.
  • Wilson CA. Phylogeny of Iris based on chloroplast matK gene and trnK intron sequence data. Mol Phylog Evol. 2004;33:402-12.
  • Wilson CA. Subgeneric classification in Iris re-examined using chloroplast sequence data. Taxon. 2011;60:27-35.
  • Wollenweber E, Stevens JF, Klimo K, Kanauft J, Norbert F, Clarissa G. Cancer chemopreventive in vitro activities of isoflavones isolated from Iris germanica Planta Med. 2003;69:15-20.
  • Wu QG, Cutler DF. Taxonomic, evolutionary and ecological implications of the leaf anatomy of rhizomatous Iris species. Bot J Linn Soc. 1985;90:253-303.

Publication Dates

  • Publication in this collection
    09 Sept 2019
  • Date of issue
    2019

History

  • Received
    13 Mar 2018
  • Accepted
    16 Apr 2018
Sociedade Brasileira da Ciência das Plantas Daninhas Departamento de Fitotecnia - DFT, Universidade Federal de Viçosa - UFV, 36570-000 - Viçosa-MG - Brasil, Tel./Fax::(+55 31) 3899-2611 - Viçosa - MG - Brazil
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