Anatomy and cell wall ultrastructure of sunflower stalk rind

The anatomy and ultrastructure of sunflower stalk rind are closely related to its conversion and utilization. We studied systematically the anatomy and ultrastructure of the stalk rind using light, scanning electron, transmission electron and fluorescence microscopy. The results showed that the stalk rind consisted of phloem fibers (PF), xylem fibers (XF), vessel elements (V), ground parenchyma cells (GPC), axial parenchyma cells (APC), xylem ray parenchyma cells (XRPC), and pith ray parenchyma cells (PRPC). These cell walls were divided into the middle lamella, primary wall, and secondary wall (S). It was found that the S of PF, XF and V was further divided into three layers (S1–S3), while the S of APC, GPC, XRPC and PRPC showed a non-layered cell wall organization or differentiated two (S1, S2) to seven layers (S1–S7). Our research revealed the plasmodesmata characteristics in the pit membranes (PMs) between parenchyma cells (inter-GPCs, inter-XRPCs, and inter-PRPCs). The morphology of the plasmodesmata varied with the types of parenchyma cells. The thickness and diameter of PMs between the cells (inter-Vs, V–XF, V–APC, and V–XRPC) were greater than that of PMs between parenchyma cells. The cell corners among parenchyma cells were intercellular space. The lignification degree of vessels was higher than that of parenchyma cells and fibers. The results will provide useful insights into the biological structure, conversion and utilization of sunflower stalk rind.

Anatomy and Ultrastructure of Galls Induced by Neuroterus quercusbaccarum (Hymenoptera: Cynipidae) on Oak Leaves (Quercus robur)

The structure and ultrastructure of two developmental stages of the spangle gall induced by Neuroterus quercusbaccarum (Hymenoptera, Cynipidae) were investigated using light microscopy (LM), fluorescence microscopy (FM), and transmission (TEM) and scanning (SEM) electron microscopy. The general design of the gall structure was typical of Cynipidae, but some structural features distinguished the spangle gall. Previously undescribed, characteristic multicellular epidermal protuberances with large openings were observed in autumn on the surface of galls. These may facilitate the gas exchange between the atmosphere and the inside of the gall, thus assisting larval respiration. The larval chamber is surrounded by both a sclerenchymatous capsule and numerous cells containing calcium oxalate crystals that may both serve as protective barriers. In young galls, the nutritive tissue is a wall-less protoplasmic mass, potentially easily accessible to young larvae with delicate mandibles. Cell walls only develop at a later stage. The nutritive tissue was found to be rich in proteins and lipids, but starch grains were not observed. Cellular topology suggests that spangle galls grow by anticlinal division of marginal epidermal cells and periclinal division of subepidermal cells. Cellular proliferation (hyperplasia) also occurs in the leaf tissue near the connection with the gall peduncle, which eventually lignifies.

Uncovering the Neglected Floral Secretory Structures of Rhamnaceae and Their Functional and Systematic Significance

Rhamnaceae flowers are notably recognized by their fleshy nectary. Other types of floral secretory structures have been scarcely reported for this family. Thus, the objective of the present study was to update the occurrence of these structures in the family and to contribute to the knowledge of their morphology and systematic significance. To this end, we carried out an extensive bibliographic search on the secretory structures of the family and obtained data for 257 taxa. Additionally, we presented here novel data (surface, anatomy, and ultrastructure) for six species belonging to the main clades within Rhamnaceae. The family has a wide diversity of types of mucilage-secreting structures: epidermis, hypodermis, idioblasts, cavities, and ducts. Mucilage and phenolic idioblasts are widely distributed among the floral organs. Colleters are present in all sampled species, and these are the first reports of their occurrence in floral organs of Rhamnaceae. The information obtained about the structure, secreted content, and occurrence of the secretory structures of Rhamnaceae helped us to understand the assertive folk use of its species. The absence of mucilage and the presence of resin or mucilage cavities and ducts in some taxa may have intrafamily systematic significance.

Polypide anatomy of hornerid bryozoans (Stenolaemata: Cyclostomatida)

Bryozoans are small colonial coelomates whose colonies are made of individual modules (zooids). Like most coelomate animals, bryozoans have a characteristic body wall composition, including epidermis, extracellular matrix (ECM) and coelothelium, all pressed together. The order Cyclostomatida, however, presents the most striking deviation, in which the ECM and the corresponding coelothelium underlying major parts of the skeletal wall epidermis are “;peeled off” to form an independent membranous sac. The polypide anatomy and ultrastructure of this group is best known from one family, the Crisiidae (Articulata). Here we examined four species from the phylogenetically and ecologically contrasting family Horneridae (Cancellata) from New Zealand. Here we provide the first detailed ultrastructural examination of the hornerid polypide, including tentacles, mouth region, digestive system and the funiculus. We were able to trace continuity and transitions of cell and ECM layers throughout the whole polypide. In addition we identified that the funiculus is a lumen-free ECM cord with two associated muscles, disconnected from interzooidal pores. While agreeing with the general cyclostomate body plan, hornerids have some unique traits that make them worthy of additional study.HighlightsHornerids share a general cyclostomate body plan. The frontal tentacle ECM transitions into oral sphincter ECM, the abfrontal lophophore ECM becomes a septum between coelomic compartments, and the funuculus is a solid ECM cord supplied with muscles.

Anatomy and Ultrastructure of the Cyprid Temporary Adhesive System in Two Species of Acorn Barnacle

Acorn barnacles are sessile as adults and select their settlement site as a cypris larva. Cyprids are well adapted to exploring surfaces in dynamic environments, using a temporary adhesive secreted from the antennules to adhere during this process. The temporary adhesive and the secretory structures are poorly characterized. This study used serial block-face scanning electron microscopy and three-dimensional modelling to elucidate the anatomy related to temporary adhesion. The temporary adhesive glands of two acorn barnacle species, Balanus amphitrite and Megabalanus coccopoma, were located in the proximal region of the first antennular segment, contrary to previous descriptions that placed them in the more distal second segment. The temporary adhesive systems of these acorn barnacles are therefore similar to that described for the stalked barnacle, Octolasmis angulata, although not identical. Knowledge of the true location of the temporary adhesive glands will underpin future studies of the production, composition and secretion of the adhesive.

Glandular trichomes of Robinia viscosa Vent. var. hartwigii (Koehne) Ashe (Faboideae, Fabaceae)—morphology, histochemistry and ultrastructure

Main Conclusion Permanent glandular trichomes of Robinia viscosa var. hartwigii produce viscous secretion containing several secondary metabolites, as lipids, mucilage, flavonoids, proteins and alkaloids. Abstract Robinia viscosa var. hartwigii (Hartweg’s locust) is an ornamental tree with high apicultural value. It can be planted in urban greenery and in degraded areas. The shoots, leaves, and inflorescences of this plant are equipped with numerous persistent glandular trichomes producing sticky secretion. The distribution, origin, development, morphology, anatomy, and ultrastructure of glandular trichomes of Hartweg's locust flowers as well as the localisation and composition of their secretory products were investigated for the first time. To this end, light, scanning, and transmission electron microscopy combined with histochemical and fluorescence techniques were used. The massive glandular trichomes differing in the distribution, length, and stage of development were built of a multicellular and multiseriate stalk and a multicellular head. The secretory cells in the stalk and head had large nuclei with nucleoli, numerous chloroplasts with thylakoids and starch grains, mitochondria, endoplasmic reticulum profiles, Golgi apparatus, vesicles, and multivesicular bodies. Many vacuoles contained phenolic compounds dissolved or forming various condensed deposits. The secretion components were transported through symplast elements, and the granulocrine and eccrine modes of nectar secretion were observed. The secretion was accumulated in the subcuticular space at the trichome apex and released through a pore in the cuticle. Histochemical and fluorescence assays showed that the trichomes and secretion contained lipophilic and polyphenol compounds, polysaccharides, proteins, and alkaloids. We suggest that these metabolites may serve an important function in protection of plants against biotic stress conditions and may also be a source of phytopharmaceuticals in the future.