The seeds of Loasaceae subfam. Loasoideae (Cornales) II: Seed morphology of “South Andean Loasas” (Loasa, Caiophora, Scyphanthus and Blumenbachia)

South Andean Loasas (Blumenbachia, Caiophora, Loasa, Scyphanthus) are a monophyletic group of taxa within Loasaceae subfam. Loasoideae, comprising some 100 species, 49 of which are investigated here. They retain a many-layered testa in the mature seeds and usually have passive transfer testas with complex, spongiose wall outgrowths. Additional modifications concern the undulations of the testa epidermis, presence or absence of the outer periclinal wall, secondary sculpturing, the presence or absence of spines, warts and finally spongiose structures on the anticlinal walls of the testa epidermis and the inner periclinal wall. Seeds of the widespread “deeply pitted” type are plesiomorphic, while various subclades of South Andean Loasas have derivations underscoring their relationships and confirming the relationships found with molecular markers and other morphological characters. The genus Blumenbachia has either seeds with a many-layered testa forming longitudinal lamellae (sect. Angulatae), or balloon seeds with a loose outer testa layer and spongiose wall outgrowths on the inner periclinal walls (sect. Blumenbachia and sect. Gripidea) and is clearly monophyletic. Loasa s.str. (ser. Loasa, ser. Macrospermae, ser. Floribundae, ser. Deserticolae) is characterized by the presence of a subterminal hilum or hilar scar and one subgroup (ser. Loasa, ser. Macrospermae) by very large and heavy seeds with a collapsed testa. L. ser. Pinnatae, ser. Acaules, ser. Volubiles, Scyphanthus and Caiophora share more or less one seed types with minor modifications. Within Caiophora various derivations are observed, of which the gradual loss of the secondary sculpture of the inner periclinal wall is the most striking one. Anemochoria is the most widespread dispersal mechanism in South Andean Loasas and is achieved in at least five structurally different ways.     

SYSTEMATIC SIGNIFICANCE OF SEED-SURFACE FEATURES IN ORTHOCARPUS (SCROPHULARIACEAE—SUBTRIBE CASTILLEJINAE)

Scanning electron microscope and light microscope examination of seed-coat features of 26 species of Orthocarpus have allowed recognition of many species-level differences (summarized in a key) and of three seed-coat types that parallel taxonomic subgroups but support realignments at generic and infrageneric levels. Type 1 seeds (subg. Orthocarpus, sect. Orthocarpus) have a lateral hilum, sculptured inner tangential seed-coat walls, and a tightly fitting outer seed coat. They are very similar to seeds of Cordylanthus. Seeds of Types 2 and 3 have a terminal hilum and membranous inner tangential cell walls. Type 2 seeds (subg. Orthocarpus, sects. Castillejoides and Cordylanthoides, with one exception) have a net-like, loosely fitting outer seed coat that shows close relationship to seeds of Castilleja. Inner tangential walls of Type 2 seeds normally rupture. Type 3 seeds (subg. Triphysaria, with two exceptions) have a tightly fitting outer seed coat and inner tangential walls are always retained. Seed features support evidence from floral morphology and chromosome numbers that Orthocarpus as currently recognized is not a monophyletic lineage.     

Seed morphology of Erica L. sect. Loxomeria Salisb. ex Benth., sect. Eremocallis Salisb. ex Benth. and sect. Brachycallis I. Hansen,and its systematic implications

Abstract

Several quantitative and qualitative seed characters of the seven European species of Erica sect. Loxomeria, Eremocallis and Brachycallis were studied. Two main seed types are found based on size and shape: regular ellipsoid or oblong seeds of ca. 0.4 mm for E. ciliaris and the E. tetralix group, and curved to kidney‐shaped seeds of 0.6–0.9 mm for E. cinerea, E. maderensis and E. terminalis. The testa surface in E. ciliaris is reticulate, with indented outer periclinal walls. Erica cinerea has inflated outer anticlinal walls. This character is exclusive for this species within the European (and nearby areas) species of the genus. The seeds of E. maderensis are similar to those of E. terminalis. According to seed morphology, the classical infrageneric classification, by which E. terminalis would be grouped with the E. tetralix group in sect. Eremocallis and E. maderensis in sect. Brachycallis with E. cinerea, is artificial.     

Anatomy of Brazilian Eriocaulaceae: correlation with taxonomy and habitat using multivariate analyses

In this study we present a survey on vegetative anatomy in species of Actinocephalus, Blastocaulon, Eriocaulon, Leiothrix, Paepalanthus, Philodice, Syngonanthus, and Tonina (Eriocaulaceae). Multivariate analyses were used to correlate anatomical characters to taxa and the habitats where the species occur. Root and stem anatomical characters seem to be more affected by environmental factors where these species occur, and seem of little value for delimiting major taxonomic groups within the family. Other characters in the leaves, such as epidermis with thickened wall cells, compartmented substomatal chambers, mesophyll with hypodermis, compact chlorenchyma, collenchymatous bundle sheath extensions, and numerous vascular bundles, were shown to be important for defining species clusters in Leiothrix, Syngonanthus, and Paepalanthus subg. Platycaulon. Similarly, loosely aggregated chlorenchyma caused Blastocaulon, Eriocaulon, Philodice, Syngonanthus sect. Carpocephalus, S. sect. Syngonanthus, and Tonina, genera from humid environments, to cluster. Scape characters appear to be more informative in discriminating groups. This situation probably reflects lower selection pressures determining anatomical characters of this organ.     

Developmental anatomy and morphology of the ovule and seed of heliconia (heliconiaceae, zingiberales)

The developmental anatomy and morphology of the ovule and seed in several species of Heliconia were investigated as part of an embryological study of the Heliconiaceae and to provide a better understanding of their relationships with the other families of the Zingiberales. Heliconia species have an ovule primordium with an outer integument of both dermal and subdermal origin. The archesporial cell is divided into a megasporocyte and a single parietal cell, which in turn are divided only anticlinally to form a single parietal layer, disintegrating later during gametogenesis. The embryo sac was fully developed prior to anthesis. In the developing seed, the endosperm was nuclear, with wall formation in the globular stage; a nucellar pad was observed during embryo development, but later became compressed. The ripe fruit contained seeds enveloped by a lignified endocarp that formed the pyrenes, with each pyrene having an operculum at the basal end; the embryo was considered to be differentiated. Most of these characteristics are shared with other Zingiberales, although the derivation of the operculum from the funicle and the formation of the main mechanical layer by the endocarp are unique to the Heliconiaceae.     

SEED-COAT MORPHOLOGY AND ANATOMY IN COLLOMIA (POLEMONIACEAE)

Seed-coat morphology of 14 species of Collomia (Polemoniaceae) was examined with light microscopy and scanning electron microscopy. Two seed types were observed based on surface sulpturing: Type 1—hexagonal epidermal cells forming a shallow reticulum with well-defined cell boundaries; Type 2—longitudinally ridged and irregularly arranged crater-like depressions with inconspicuous cell boundaries. Only two species, C. debilis and C. larsenii of sect. Collomiastrum have seed-coat Type 1. Seed-coat Type 2 is characteristic of all species of sect. Collomia, sect. Courtoisia, and C. mazama, C. rawsoniana of sect. Collomiastrum. The present investigation reveals a fairly homogeneous seed-coat pattern in the genus and does not offer significant information for realignment of infrageneric classification. Anatomical studies with light microscopy show that a mucilaginous seed coat develops from the outermost layer of integument in which each epidermal cell develops spiral secondary wall thickenings. Mucilaginous seeds of most Collomia species probably provide adaptive significance in that adherence of seeds to ground prohibits further dispersal to unfavorable habitats, or epizoochoric dispersal.     

Floral anatomy of Paepalanthoideae (Eriocaulaceae, Poales) and their Nectariferous structures

BACKGROUND AND AIMS: Eriocaulaceae (Poales) is currently divided in two subfamilies: Eriocauloideae, which comprises two genera and Paepalanthoideae, with nine genera. The floral anatomy of Actinocephalus polyanthus, Leiothrix fluitans, Paepalanthus chlorocephalus, P. flaccidus and Rondonanthus roraimae was studied here. The flowers of these species of Paepalanthoideae are unisexual, and form capitulum-type inflorescences. Staminate and pistillate flowers are randomly distributed in the capitulum and develop centripetally. This work aims to establish a floral nomenclature for the Eriocaulaceae to provide more information about the taxonomy and phylogeny of the family. METHODS: Light microscopy, scanning electron microscopy and chemical tests were used to investigate the floral structures. KEY RESULTS: Staminate and pistillate flowers are trimerous (except in P. flaccidus, which presents dimerous flowers), and the perianth of all species is differentiated into sepals and petals. Staminate flowers present an androecium with scale-like staminodes (not in R. roraimae) and fertile stamens, and nectariferous pistillodes. Pistillate flowers present scale-like staminodes (except for R. roraimae, which presents elongated and vascularized staminodes), and a gynoecium with a hollow style, ramified in stigmatic and nectariferous portions. CONCLUSIONS: The scale-like staminodes present in the species of Paepalanthoideae indicate a probable reduction of the outer whorl of stamens present in species of Eriocauloideae. Among the Paepalanthoideae genera, Rondonanthus, which is probably basal, shows vascularized staminodes in their pistillate flowers. The occurrence of nectariferous pistillodes in staminate flowers and that of nectariferous portions of the style in pistillate flowers of Paepalanthoideae are emphasized as nectariferous structures in Eriocaulaceae.     

Anatomy and ontogeny of Pterodon emarginatus (Fabaceae: Faboideae) seed.

The aim of this study was to describe the anatomy and ontogeny of Pterodon emarginatus seed using the usual techniques. The ovules are campilotropous, crassinucelate, and bitegmic. The following processes occur during integument development: anticlinal divisions and phenolic compound accumulations in the exotesta, whose cells become palisade; predominantly periclinal divisions and cell expansion in the mesotesta, where the rapheal bundle differentiates; differentiation of the hourglass-cell layer adjacent to the palisade; fusion of outer and inner integuments, which remain individualized structures only at the micropylar end; and intense pectin impregnation in the mesotesta thicker walls with lignification restricted to the xylem. At the hilar pole, the Faboideae seed characteristic structure develops, with double palisade layer, subhilar parenchyma, and tracheid bar. The younger nucellus shows thicker pectic cell walls and is consumed during seed formation. The endosperm is nuclear and, after cellularization, shows peripheral cells with dense lipid content; the seeds are albuminous. The axial embryo shows fleshy cotyledons, which accumulate lipid and protein reserves; starch is rare. Although the seed structure is characteristic of the Fabaceae, the inner integument coalesces into the outer integument without being reabsorbed.     

Studies on Mature Seeds of Cuscuta pedicellata and C. campestris by Electron Microscopy

The seeds of Cuscuta pedicellata have been investigated by transmissionand scanning electron microscopy. Additional observations havebeen made on seeds of C. campestris by SEM only. The seed coatconsists of an outer single epidermis, two different palisadelayers, and an inner multiparenchyma layer. The outer epidermalwall in C. pedicellata has a thick cuticle and zones rich inpectic substances. The thicker ‘U-shaped’ cell wallsin the outer palisade layer are strengthened by a wall layerof hemicellulose. The inner palisade layer has thick walledcells with a ‘light line’. The inner cell wall ofthe compressed multiparenchyma layer has a thin cuticle. A fairlythick cuticle is positioned directly on the endosperm surface.The aleurone cell walls are different from the remaining endospermwalls. The latter are thick and believed to be of galactomannans.There is a ‘clear’ zone between the plasmalemmaand the cell wall in the aleurone cells. The embryo cells arepacked with lipids and proteins. In Cuscuta campestris mostendosperm has been absorbed during the seed development. Theembryo apex has two minute leaf primordia. The features of theCuscuta seeds are discussed in relation to functional and environmentalconditions. Cuscuta pedicellata, Cuscuta campestris, seed, seed coat, cuticle, cell walls, endosperm, aleurone cells, galactomannan, embryo, TEM, SEM     

Development of the ovule and seed in Costus cuspidatus (N.E.Br.) Maas (Zingiberaceae), with special reference to the formation of the operculum

The ovule primordium of Costus is trizonate and both its integuments are dermally initiated. With other evidence, this strongly suggests that most, if not all, monocotyledons have dermally initiated integuments, indicating a derived status. The mature seed coat of Costus is completely formed by the outer integument and its principal mechanical layer is the endotesta.
The seed of Costus has an aril, an operculum and a micropylar collar. These structures, characteristic of zingiberalean seeds, are each initiated in a different, specific cell layer of the exostome. The aril is completely dermally initiated. The parenchymatic part of the operculum and the micropylar collar are of dual origin, namely dermal at me integumentary region and subdermal at the raphe.     

Seed structure and systematic position ofHampea nutricia (Malvaceae)

The mature seeds ofHampea nutricia are glabrous, ovoid, arillate and dark tan in colour. Longitudinal streaks on the seed surface correspond to the underlying integumentary vascular strands. Testa and tegmen are derived from the outer and inner integuments, respectively. The outer epidermis of the tegmen forms a palisade-like macrosclereid layer, the inner epidermis a fringe layer. The endosperm is single-layered and also fills the space between the two cotyledons. The embryo is nearly straight, gland-dotted; it has asymmetrical and folded cotyledons, and gossypol ducts. Systematic position ofHampea is discussed and its placement inMalvaceae is supported.     

On the Embryogeny of Three Taxa of Paepalanthoideae (Eriocaulaceae)

Embryo development in Leiothrix nubigena, Paepalanthus bifidusand Syngonanthus nitens is described. Distinct differentiationof cotyledonary and epicotyledonary sectors in the three taxais demonstrated. The cotyledonary and the epicotylary loci shareequal amounts of the embryonic shoot apex as in most monocotyledons.The cotyledon and its adjacent epicotyl are both terminal onthe embryonic axis. The basal cell of the two-celled proembryocontributes two basal rows of cells at the radicular pole inthe ripe seed. A typical radicle is not organized. Leiothrix nubigena, Paepalanthus bifidus, Syngonanthus nitens Paepalanthoideae, Eriocaulaceae, embryogeny     

Seed development and function inArtabotrys hexapetalus (Annonaceae)

Until now seeds ofAnnonaceae were characterized as mesotestal only. The seed ofArtabotrys hexapetalus, however, is meso- and endotestal. An outer mechanical layer which surrounds the seed as a lignified fibrous tissue is derived from the mesotesta. A complex inner mechanical layer develops from a partially multi-layered endotesta built up by crystal-containing stone cells. The multi-layered endotesta forms a prominent seed plug in the micropylar region which is prolonged along both sides of the perichalaza as inner walls. The endotesta is one-layered on the sides of the seed and participates in rumination. In addition the endotesta may serve for deposition of end-products of metabolism. The complex growing process of the perichalaza and its surrounding tissues is described in detail. The perichalazal pad of tanniferous cells forms an U-shaped septum, in conjunction with the endotesta, dividing the seed into two chambers. During seed development it functions as transmitter of nutrients from the outer chamber filled with starch grains to the nucellus, endosperm and embryo contained in the inner one. During germination this pad probably serves for the uptake of water. — At the initial phases of germination the seed dehisces into two valves along the raphal and antiraphal side. Later on an additional parenchymatous operculum covering the seed apex disintegrates and the endotestal plug fixed by its two prolongations splits along a preformed fracture line into two parts to release the seedling. Rudiments of an aril are recognizable in young seeds only. — The data obtained fromArtabotrys hexapetalus are discussed and compared with published information on seeds in other annonaceous taxa. For systematic considerations the necessity to define the origin of the annonaceous seed plug from one or the other integument is emphasized as it may prove to be an important differential character withinAnnonaceae.     

Datura stramonium Agglutinin : Location in the Seed and Release upon Imbibition

The distribution of Datura stramonium agglutinin over different tissues of D. stramonium L. seeds was visualized by immunocytochemical techniques and quantified by agglutination assays. The lectin occurs predominantly in the outer seed tissues (seed coat and seed epidermis), where it is associated, at least in part, with the cell walls. Developing D. stramonium seeds secrete newly synthesized lectin polypeptides into the incubation medium, which confirms the extracellular location of the lectin. Imbibition of mature decoated seeds results in a rapid and highly specific release of lectin. Indeed, imbibition solutions contain almost exclusively the lectin together with a few other carbohydrate-binding proteins; this is indicative of the predominance of these proteins in the seed surface layer. The presence of important amounts of lectin in the outer tissues of the seed is consistent with a possible role in the mediation of cell-cell interactions.     

Seed morphology and endosperm structure of selected species of Primulaceae, Myrsinaceae, and Theophrastaceae and their systematic importance

Seed size and shape, seed coat surface pattern, seed coat thickness, and endosperm structure were investigated in Androsace septentrionalis, Cortusa matthioli, Hottonia palustris, Primula elatior, Soldanella carpatica (Primulaceae), Anagallis arvensis, A. minima, Cyclamen purpurascens, Glaux maritima, Lysimachia nemorum, L. vulgaris, Trientalis europaea (Myrsinaceae), and Samolus valerandi (Theophrastaceae). Three seed size categories were distinguished on the basis of biometric measurements. Almost all seeds examined were found to be small with an angular shape classified as sectoroid or polyhedral. A new type of seed shape, suboval, was identified for H. palustris. Cyclamen purpurascens seeds differed from seeds of all other species examined because of their large size, subglobose shape, and concave hilar area. Despite the different shape types, the length/width ratio of the seeds examined was constant, while their hilum length/width ratio was a highly variable feature. Three types of seed surface patterns were observed: (1) reticulate, (2) tuberculate with secondary striations, and (3) poroid-alveolate with the presence of a spongy outer layer. For seeds of Anagallis arvensis, A. minima, Cortusa matthioli, Lysimachia nemorum, and Soldanella carpatica, secondary seed sculpture was described. The seed coats of all species examined were two-layered, and great differences in testa thickness were found (9.9?C128.6???m). In general, seeds of the Myrsinaceae species were more often characterized by thick testa. Different proportions in thickness of the inner and outer testa layers were observed. In seeds with reticulate seed patterns, the inner testa layer was twice to several times thicker than the outer layer, while the opposite proportions were observed in seeds with the tuberculate or poroid-alveolate seed sculpture pattern. In seeds of all species examined, oxalate crystals were present on the surface of the inner testa layer. Thus, the presence or absence of oxalate crystals in testa is not a feature distinguishing species with angular or subglobose seeds. Four types of endosperm structure were identified according to the thickness of the endosperm cell walls and the relief of their inner surface: (1) with evenly thickened and smooth cell walls, (2) with evenly thickened cell walls and circular or helical thickenings on their inside surfaces, (3) with very thick, but not evenly thickened cell walls with constrictions (??pitted??), and (4) with very thin papery and undulate cell walls. There is no rule concerning the seed shape, type of the seed sculpture, testa thickness, or endosperm structure that corresponds to the family affiliation of the species examined.     

Seed coat morphology and its systematic significance in Juncus L. (Juncaceae) in Egypt

The seed morphology of nine taxa of Juncus from Egypt has been investigated using light and scanning electron microscopy, to determine the importance of seed coat features as taxonomic characters. Macro- and micromorphological characters, including seed shape, color, size, seed appendages, epidermal cell shape, anticlinal boundaries, and outer periclinal cell wall and secondary cell wall sculpture are presented. Four types of seed appendages are recognized: (i) seeds with two appendages; (ii) seeds without appendages; (iii) seeds with minutely a piculate at one end; and (iv) seeds with minutely a piculate at both ends. Two types of anticlinal cell wall boundaries,(i) raised-channeled, straight and (ii) raised, straight or sinuous, and three different shapes of outer periclinal cell wall are described: (i) flat; (ii) concave; and (iii) flat to slightly concave. The secondary sculpture of the cell wall varies from striate to microreticulate or reticulate, and smooth to finely folded. Seed characters provide useful data for formulating the taxonomy of Juncus both on the subgeneric and sectional level. A key for the identification of the investigated taxa based on seed characters is provided.     

Seed coat morphology and its systematic significance in Juncus L. (Juncaceae)in Egypt

The seed morphology of nine taxa of Juncus from Egypt has been investigated using light and scanning electron microscopy,to determine the importance of seed coat features as taxonomic characters.Macro-and micromorphological characters,including seed shape,color,size,seed appendages,epidermal cell shape,anticlinal boundaries,and outer periclinal cell wall and secondary cell wall sculpture are presented.Four types of seed appendages are recognized:(i)seeds with two appendages;(ii)seeds without appendages;(iii)seeds with minutely a piculate at one end;and(iv)seeds with minutely a piculate at both ends.Two types of anticlinal cell wall boundaries,(i)raised-channeled,straight and(ii)raised,straight or sinuous,and three different shapes of outer periclinal cell wall are described:(i)flat;(ii)concave;and(iii)flat to slightly concave.The secondary sculpture of the cell wall varies from striate to microreticulate or reticulate,and smooth to finely folded.Seed characters provide useful data for formulating the taxonomy of Juncus both on the subgeneric and sectional level.A key for the identification of the investigated taxa based on seed characters is provided.     

Posttranslational regulation of pyruvate, orthophosphate dikinase in developing rice (Oryza sativa) seeds

Pyruvate, orthophosphate dikinase (PPDK; E.C.2.7.9.1) is most well known as a photosynthetic enzyme in C₄ plants. The enzyme is also ubiquitous in C₃ plant tissues, although a precise non-photosynthetic C₃ function(s) is yet to be validated, owing largely to its low abundance in most C₃ organs. The single C₃ organ type where PPDK is in high abundance, and, therefore, where its function is most amenable to elucidation, are the developing seeds of graminaceous cereals. In this report, we suggest a non-photosynthetic function for C₃ PPDK by characterizing its abundance and posttranslational regulation in developing Oryza sativa (rice) seeds. Using primarily an immunoblot-based approach, we show that PPDK is a massively expressed protein during the early syncitial-endosperm/-cellularization stage of seed development. As seed development progresses from this early stage, the enzyme undergoes a rapid, posttranslational down-regulation in activity and amount via regulatory threonyl-phosphorylation (PPDK inactivation) and protein degradation. Immunoblot analysis of separated seed tissue fractions (pericarp, embryo + aleurone, seed embryo) revealed that regulatory phosphorylation of PPDK occurs in the non-green seed embryo and green outer pericarp layer, but not in the endosperm + aleurone layer. The modestly abundant pool of inactive PPDK (phosphorylated + dephosphorylated) that was found to persist in mature rice seeds was shown to remain largely unchanged (inactive) upon seed germination, suggesting that PPDK in rice seeds function in developmental rather than in post-developmental processes. These and related observations lead us to postulate a putative function for the enzyme that aligns its PEP to pyruvate-forming reaction with biosynthetic processes that are specific to early cereal seed development.     

A subtilisin-like serine protease essential for mucilage release from Arabidopsis seed coats

During Arabidopsis seed development large quantities of mucilage, composed of pectins, are deposited into the apoplast underneath the outer wall of the seed coat. Upon imbibition of mature seeds, the stored mucilage expands through hydration and breaks the outer cell wall that encapsulates the whole seed. Mutant seeds carrying loss-of-function alleles of AtSBT1.7 that encodes one of 56 Arabidopsis thaliana subtilisin-like serine proteases (subtilases) do not release mucilage upon hydration. Microscopic analysis of the mutant seed coat revealed no visible structural differences compared with wild-type seeds. Weakening of the outer primary wall using cation chelators triggered mucilage release from the seed coats of mutants. However, in contrast to mature wild-type seeds, the mutant's outer cell walls did not rupture at the radial walls of the seed coat epidermal cells, but instead opened at the chalazal end of the seed, and were released in one piece. In atsbt1.7, the total rhamnose and galacturonic acid contents, representing the backbone of mucilage, remained unchanged compared with wild-type seeds. Thus, extrusion and solubility, but not the initial deposition of mucilage, are affected in atsbt1.7 mutants. AtSBT1.7 is localized in the developing seed coat, indicating a role in testa development or maturation. The altered mode of rupture of the outer seed coat wall and mucilage release indicate that AtSBT1.7 triggers the accumulation, and/or activation, of cell wall modifying enzymes necessary either for the loosening of the outer primary cell wall, or to facilitate swelling of the mucilage, as indicated by elevated pectin methylesterase activity in developing atsbt1.7 mutant seeds.