Paiva Elder Antônio Sousa
Departamento de Botânica, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, 31270-901 - Belo Horizonte, MG, Brazil.
Ann Bot. 2009 Oct;104(5):937-44. doi: 10.1093/aob/mcp175. Epub 2009 Jul 17.
The occurrence of nectaries in fruits is restricted to a minority of plant families and consistent reports of their occurrence are not found associated with Fabaceae, mainly showing cellular details. The present study aims to describe the anatomical organization and ultrastructure of the pericarpial nectaries (PNs) in Erythrina speciosa, a bird-pollinated species, discussing functional aspects of these unusual structures.
Samples of floral buds, ovaries of flowers at anthesis and fruits at several developmental stages were fixed and processed by the usual methods for studies using light, and scanning and transmission electron microscopy. Nectar samples collected by filter paper wicks were subjected to chemical analysis using thin-layer chromatography.
The PNs are distributed in isolation on the exocarp. Each PN is represented by a single hyaline trichome that consists of a basal cell at epidermal level, stalk cell(s) and a small secretory multicellular head. The apical stalk cell shows inner periclinal and anticlinal walls impregnated by lipids and lignin and has dense cytoplasm with a prevalence of mitochondria and endoplasmic reticulum. The secretory cells show voluminous nuclei and dense cytoplasm, which predominantly has dictyosomes, rough endoplasmic reticulum, plastids, mitochondria and free ribosomes. At the secretory stage the periplasmic space is prominent and contains secretion residues. Tests for sugar indicate the presence of non-reducing sugars in the secretory cells. Nectar samples from PNs contained sucrose, glucose and fructose.
The secretory stage of these PNs extends until fruit maturation and evidence suggests that the energetic source of nectar production is based on pericarp photosynthesis. Patrolling ants were seen foraging on fruits during all stages of fruit development, which suggests that the PNs mediate a symbiotic relationship between ants and plant, similar to the common role of many extrafloral nectaries.
果实蜜腺的出现仅限于少数植物科,且未发现豆科植物有关于其出现的一致报道,主要是关于细胞细节方面。本研究旨在描述刺桐(Erythrina speciosa)(一种鸟类传粉的物种)果皮蜜腺(PNs)的解剖结构和超微结构,并讨论这些不寻常结构的功能方面。
采集花芽、花期花朵的子房以及几个发育阶段果实的样本,采用常规方法进行固定,用于光学显微镜、扫描电子显微镜和透射电子显微镜研究。用滤纸芯收集的花蜜样本采用薄层色谱法进行化学分析。
PNs孤立地分布在外果皮上。每个PN由单个透明毛状体代表,该毛状体由表皮水平的基部细胞、柄细胞和一个小的分泌性多细胞头部组成。顶端柄细胞的内平周壁和垂周壁被脂质和木质素浸渍,细胞质致密,富含线粒体和内质网。分泌细胞的细胞核大且细胞质致密,主要含有高尔基体、糙面内质网、质体、线粒体和游离核糖体。在分泌阶段,周质空间突出,含有分泌残留物。糖类检测表明分泌细胞中存在非还原糖。PNs的花蜜样本中含有蔗糖、葡萄糖和果糖。
这些PNs的分泌阶段一直持续到果实成熟,有证据表明花蜜产生的能量来源基于果皮光合作用。在果实发育的各个阶段都能看到巡逻的蚂蚁在果实上觅食,这表明PNs介导了蚂蚁与植物之间的共生关系,类似于许多花外蜜腺的常见作用。