The Brassicaceae (Cruciferae), or mustard family, is one of the largest angiosperm families, can be recognized easily by its floral and fruiting characters. It is cosmopolitan but chiefly distributed in the temperate and Mediterranean region, it represented by 338 genera and 3709 species [1] . In Saudi Arabia, it is represented by 53 genera and 74 species [2] . In eastern region of Saudi Arabia, [3] recorded 46 species and 30 genera.

The morphological characters of the family Brassicaceae especial fruit seed and cotyledons are used in the tribal classification of the family [4] recognized 10 tribes based on fruit and cotyledon characters. [5] recognized 4 tribes and 19 sub tribe, then [6] put the members of the family in 10 tribes by using nectar glands and myrosin cells characters. [7] divided the family into three groups according to fruit characters into Siliquosae, Siliqulosae and Lomentaeae, each composed of number of tribes. [8] classifies the genera of the family in 19 tribes. [9] reduced the total number of Schulz’s tribes from 19 to 15 tribes depending on very large numbers of features of flowers and fruit. [10] recognized 6 tribes under the family Cruciferae according to fruit characters, but [11] divided the family into 6 groups and 10 tribes. [12] [13] reduced Schulz’s tribes to three tribes: The lypodieae, Brassiceae and Sisymbrieae. [14] classified the family Brassicaceae of the southeastern United States into 7 tribes; then [15] recognized 25 tribes for the family Brassicaceae. Recently there are some researches based on molecular and phylogenetic studies for the family as [16] - [29] .

The morphology of seed coat structure is considered to be stable characters and is little influenced by external environmental conditions whilst the seeds develop and ripen within the fruit [30] [31] [32] [33] . The seed coat characters have been used successfully to solve systematic and phylogenetic problems between different taxa [34] [35] . In the Brassicaceae, several studies have been carried out on the seed coat and its taxonomic significance. [36] [37] [38] [39] studied the external morphology and anatomy of seeds of 90 genera and 200 species of the Cruciferae. [40] [41] [42] investigated the seed coats and development of epidermal slime bodies of Malcolmia. [43] studied the seed coat of Lepidium in East tropical Africa. [44] investigated the structure of seed coat and development in certain species of Brassicaceae. [45] [46] studied some taxa of Brassica seeds by using scanning electron microscope (SEM). [47] used SEM on the seed surface to distinguish Matthiola, Morettia, and Diceratella. [48] studied the seed coat morphology, particularly the epidermal slime structure of Morettia. [49] studied the seed coat of genus Farsetia by using SEM to distinguish between species. [50] investigated the seed coat sculpture in species of the tribe Brassiceae in Egypt by using SEM. [51] investigated the seed morphology and taxonomy with SEM in the tribe Lepidieae in Egypt. More recently, [52] gave detailed descriptions of seed morphology in 44 species of the subtribes Brassicinae, Raphaninae and Moricandiinae, and elucidated the phylogenetic relationships between taxa. [53] study seed morphology of 45 taxa belonging to 23 genera from tribes Arabideae, Euclidieae, Hesperideae, Lunarieae, Matthioleae, and Sisymbrieae, of Brassicaceae were examined using light and scanning electron microscopy. [54] studied the macro and micromorphological characters of approximately 22 genera, 30 species of Brassicaceae. [55] study seed coat sculpture of 93 taxa belonging to 45 genera of the family Brassicaceae from Egypt by using light and scanning electron microscope. [56] investigated seed morphology and seed coat sculpturing of 32 Taxa of Family Brassicaceae by using light microscope and scanning electron microscope. [57] study the relation between 26 taxa of family Brassicaceae from Egypt by using morphological characters including fruit and seed characters, [58] study the seed exomorphic characteristics of 14 taxa of Lepidium L. in Brassicaceae from Turkey by light microscope and scanning electron microscope (SEM). [59] study macro and micromorphological characters of 9 species and 30 accessions seeds in Ricotia L. by light (LM) and scanning electron microscopy (SEM) to evaluate the taxonomic relevance of these traits. [60] studies the morphological Characteristics of some species of Brassicaceae (Cruciferous) in Setifian High Plateau, Algeria.

The fruit and seed coat morphological feature in Brassicaceae species growing in eastern region of Saudi Arabia is not yet correctly projected. Therefore, our knowledge about the fruit and seed coat morphology of these plants is only measly. Therefore the main objective of this study is to examine and describe the fruit and seed coat of some species of Brassicaceae growing in eastern region of Saudi Arabia by using light and scanning electron microscope to indicate the important of these characters for taxonomy and identification of different species.

Ten species belong to nine genera were collected fresh in spring season from different area in eastern region of Saudi Arabia (Table 1). The materials studied were identified according to plant key of [2] [3] . Foliar details for fruit and seed were examined with the aid of binocular stereo microscope (Olympus Bx53). The details of seed morphology were investigated in electron scanning microscope (SEM) with the use of FEI, ISPECT S50 (Czech Republic). SEM was operated at 20 kV with working distance 10 mm. Long and high magnification was performed to capture the recognized features of the specimen. The seeds were

mounted onto a metallic stub with a double-sided adhesive tape. Gold coating of few nanometers was applied using sputter coating machine (Quorum, Q150R ES, UK) to avoid charging and capture high quality images.

The terminology of [32] [61] [62] was adopted to describe the SEM aspects of the seed coat. The morphological characters of the fruit and seed for the studied species were collected and creating data matrix used for numerical analysis. The relationships between the studied species have been demonstrated as dendrograms Figure 4 by using PRIMER 6, version 6.1.6 analyses using agglomeration of Schedule measure Euclidean distance, using complete linkage between groups.

The fruit and seed morphological characters for ten species of the family Brassicaceae are summarized in Tables 2-6 and the image by and SEM are represented in Figures 1-3.

The fruit and seed morphology characters of the studied species obtained by light and scanning electron microscope 34 characters (14 characters for fruit and 20 characters for seed) were used for numerical analysis.

The cluster analysis obtained from fruit characters only (Figure 4(a)) showed that species were grouped into two major clusters and each cluster divided into two groups, the first cluster I consisted of five species: Coronopus didymus and Farsetia burtonae recorded in group I while Cardamine hirsute, Cakile arabica and Sisymbrium irio present in group II. The cluster II comprised five species: Raphanus sativus (group I) and Brassica juncea, Eruca sativa, Brassica tournefortii and Savignya parviflora (group II).

The results obtained from seed characters only (Figure 4(b)) also divided the studied species into two main clusters and two groups. Cluster I contained Savignya parviflora and Farsetia burtonae. While cluster II consisted of eight species present in two groups; Cardamine hirsute, Raphanus sativus, Coronopus didymus, Eruca sativa and Cakile arabica in group I and Brassica juncea, Brassica tournefortii and Sisymbrium irio in group II.

The results obtained from combined of fruit and seed characters (Figure 4(c)) divided the species into two main clusters and two groups. Cluster I contained

Savignya parviflora and Farsetia burtonae. While cluster II consisted of eight species present in two groups; Cardamine hirsute, Raphanus sativus, Cakile arabica, Eruca sativa and Sisymbrium irio in group I and Brassica juncea, Brassica tournefortii and Coronopus didymus in group II.

The tribal classification of Brassicaceae has long been problematic and not well understood phylogenetically because of the traditionally used few characters as cotyledons in the embryo, fruit characters, number of rows of seeds in each locule, trichome type, and features of the nectarines etc. to delimit different tribes of the family Brassicaceae [23] [63] . In the present study, the species are recorded in five tribes (Alysseae, Lepideae, Sisymbrieae, Cardamineae, Brassiceae) [15] .

The tribe Alysseae DC. As delimited by [15] [64] are polyphyletic. It consists of approximately 280 species, the Farsetia species put in different tribes in different studies; [5] put it in tribe Hesperideae under subtribe Malcolmiinae while [7] placead the Farsetia species with Lobularia in tribe Alyssineae, [10] put it in tribe Arabideae. Recently [15] put the species Farsetia in tribe Alysseae as [8] . The tribe has recently been studied phylogenetically as [65] [66] . The position of Alysseae relative to the other tribes varied in different studies; [20] put the tribe with tribe Brassiceae in lineage II, while [63] say the tribe appeared either related to Erysimum or unrelated to any tribe. [67] found the tribe related to the Noccaeeae, while [68] it grouped together with the tribes Chorisporeae, Hesperideae, and Malcolmieae. In the present study tribe Alysseae (Farsetia burtonae) are placed with tribe Lepideae (Coronopus didymus) in the cluster result from fruit characters only, this differ from the traditional classification which separate them into different tribes or different groups, but it agree with recent molecular studies as [27] which put the two tribes in the same lineage. While in the clusters results from seed or seed and fruit characters the tribe Alysseae (Farsetia burtonae) are placed with species of tribe Brassiceae (Savignya parviflora), this agree with some molecular studies as [27] [69] .

The tribe Lepideae consists of three to five genera and over 240 species, [15] [70] . It is polyphyletic. Some genetic studies as done on the tribes, [27] [69] [71] [72] [73] . In the present study the tribe Lepideae (Coronopus didymus) are placed with some species of tribe Brassiceae, this agree with some traditional studies as [5] which put them in the same tribe but in different sub-tribes, or placed with species of tribe Alysseae (Farsetia burtonae) in the same group.

The tribe Sisymbrieae was recognized with 70 genera and 400 species according to [8] [74] but molecular data as, [18] [75] [76] [77] , supported the removal of many of its component genera to other tribes. The tribe is monophyletic and is sister to the Schizopetaleae [20] or the Brassiceae [18] [75] . In the present study the tribe Sisymbrieae (Sisymbrium irio) found together with species from tribe Brassiceae, this agrees with [5] [18] [27] [69] [75] .

[9] presented a phylogenetic network and indicated close relationships of Sisymbrieae with Arabideae and Lepidieae. [78] [79] have shown that the boundaries between the tribes Lepidieae, Lunarieae, Sisymbrieae, Euclidieae, and Alysseae are highly artificial. The results from previous studies of phylogenetic relationships [71] [72] [73] demonstrated a close relationship among the tribes Sisymbrieae, Lepidieae and Arabideae. [70] indicated that the tribes Arabideae, Lepidieae and Sisymbrieae are polyphyletic.

The tribe Cardamineae DC is monophyletic. The tribe has been subjected to several molecular studies as; [80] [81] [82] [83] [84] that support its monophyly. The position of Cardamineae relative to the other tribes is done by some studies as, [27] [69] . The study put the tribe Cardamineae with tribe Lepidieae and tribe Alysseae in the same lineage. In the present study the tribe Cardamineae (Cardamine hirsute) placed together in the same group with some species of tribe Brassiceae and tribe Sisymbrieae in all clusters, this agree with [5] .

The tribe Brassiceae DC is consider monophyletic according to some molecular studies as [19] [85] [86] . This tribe was subjected to extensive molecular studies, [20] [63] [67] [69] [87] [88] . In the present study the most species of tribe Brassieae are placed together but some species present with different tribes. This results support the Brassiceae to be heterogenous.

The fruit and seed coat characters are very important characters that can be used for identification and differentiate between the different tribes and also between species belong to the same genera. Most tribes of Brassicaceae are polyphyletic, and some are related to each other’s as Lepidieae, Alyssieae and Sisymbrieae. The results indicate the tribe Brassiceae to be heterogenous.

Author is grateful to the staff of Institute for Research and Medical Consultation (IRMC) in the University of Imam Abdulrahman Bin Faisal for carry out the Scanning Electron Microscope (SEM). Also I would like to express my sincere appreciation to the research units of college Science research for giving me the opportunity to conduct the practical part research.

Gabr, D.G. (2018) Significance of Fruit and Seed Coat Morphology in Taxonomy and Identification for Some Species of Brassicaceae. American Journal of Plant Sciences, 9, 380-402. https://doi.org/10.4236/ajps.2018.93030