# Nectary Structure and Nectar Secretion Characteristics Among Various Cultivars of Paeonia lactiflora

**Authors:** Hui Cai, Wenjie Ma, Yingling Wan, Yan Liu

PMC · DOI: 10.3390/plants15040580 · Plants · 2026-02-12

## TL;DR

This study examines nectar production in Paeonia lactiflora cultivars to address contamination issues in the cut flower industry.

## Contribution

The study introduces a nectar secretion index and identifies structural and physiological factors influencing nectar production.

## Key findings

- Nectar secretion varies among P. lactiflora cultivars, with sucrose as the primary sugar component.
- Specialized raised stomata on the upper epidermis are responsible for nectar secretion, not regular stomata.
- Nectar production correlates with stomatal aperture and photosynthetic potential, not with flower type or color.

## Abstract

Background: Paeonia lactiflora Pall. produces substantial quantities of nectar during the bud stage. In the production of cut flowers, this nectar attracts contaminants that compromise the quality of the flowers. The current practice of rinsing flowers with clean water escalates production costs. Consequently, reducing nectar secretion during the bud stage has emerged as a significant technical challenge for the industry. Nonetheless, insufficient fundamental knowledge concerning the structure of P. lactiflora nectaries and the physiology of nectar secretion impedes the development of pertinent regulatory technologies. Methods: This study established a “nectar secretion index” to evaluate nectar production in various P. lactiflora cultivars. Nectar sugar concentration and composition were measured using a refractometer and gas chromatography–mass spectrometry (GC-MS). Observations of changes in nectary epidermal morphology and anatomical structure during nectar secretion were conducted using scanning electron microscopy and light microscopy. Key Results: The quantity of nectar secreted by various P. lactiflora cultivars can differ. The indices were not significantly correlated with flowering period, flower color, or flower type. At the peak of nectar secretion, the sugar concentration of nectar secretion by different cultivars’ flower buds varied. Sucrose is the primary sugar component in this nectar. Nectar is secreted along the basal margins of the bracts and sepals on the abaxial surface of all cultivars. Specialized raised stomata are located on the upper epidermis, through which nectar is secreted. In contrast, the epidermal stomata located outside nectar-secreting areas exhibit a normal morphology. Specialized stomata do not secrete nectar concurrently. The stomatal aperture and the percentage of nectar-secreting stomata at the secretion sites are significantly higher in high-nectar-producing cultivars than in low-nectar-producing cultivars. Anatomical observations of bract nectaries indicate that, irrespective of nectar production levels, specialized stomata are consistently located adjacent to vascular bundles. During the initial stage of nectar secretion, no starch was detected in the bract nectaries. In contrast, the stomata in non-secretory epidermal cells of bracts maintain a normal morphology, and calcium oxalate crystals were observed within the subepidermal tissues. Throughout the nectar secretion process, the content of photosynthetic pigments and the Fv/Fm ratio in the bracts and sepals of various cultivars correlated with nectar secretion volume. Conclusions: This study, informed by observations of numerous P. lactiflora cultivars, elucidates the structural characteristics of its nectaries and the nectar secretion properties of various cultivars during the bud stage. It confirms that these nectaries are classified as extrafloral nectaries, specifically structural nectaries consisting of specialized raised stomata and closely associated vascular bundles beneath them. No significant differences in nectary structure or location were noted among cultivars with differing nectar yields. However, both the aperture of nectary stomata and the percentage of nectar-secreting stomata exhibited a significant positive correlation with secretion levels. The intrinsic photosynthetic potential at the nectary sites varies significantly among cultivars. The nectar is not derived from stored cellular starch but likely originates simultaneously from both photosynthesis and phloem transport. These findings provide a theoretical foundation for the development of subsequent regulatory technologies.

## Linked entities

- **Chemicals:** sucrose (PubChem CID 5988), calcium oxalate (PubChem CID 33005)
- **Species:** Paeonia lactiflora (taxon 35924)

## Full-text entities

- **Diseases:** gray mold diseases (MESH:D055652), injury to (MESH:D014947)
- **Chemicals:** carbohydrates (MESH:D002241), acetone (MESH:D000096), MEJA (MESH:C072239), carbon (MESH:D002244), monosaccharides (MESH:D009005), Chlorophyll (MESH:D002734), starch (MESH:D013213), nitrogen (MESH:D009584), amino acids (MESH:D000596), stachyose (MESH:C005695), polysaccharides (MESH:D011134), phosphate (MESH:D010710), hexoses (MESH:D006601), Oligosaccharides (MESH:D009844), sugar alcohols (MESH:D013402), Sugar (MESH:D000073893), periodate (MESH:C009288), helium (MESH:D006371), gold (MESH:D006046), maltose (MESH:D008320), paraffin (MESH:D010232), raffinose (MESH:D011887), Chla (-), trisaccharides (MESH:D014312), toluidine blue (MESH:D014048), trehalose (MESH:D014199), inositol (MESH:D007294), formaldehyde (MESH:D005557), ethanol (MESH:D000431), jasmonic acid (MESH:C011006), D-ribose (MESH:D012266), glucose (MESH:D005947), alcohols (MESH:D000438), chlorophyll b (MESH:C037184), Tween-20 (MESH:D011136), glutaraldehyde (MESH:D005976), phenidone (MESH:C015429), Sucrose (MESH:D013395), disaccharides (MESH:D004187), Calcium oxalate (MESH:D002129), water (MESH:D014867), FAA (MESH:C049328), D-fructose (MESH:D005632)
- **Species:** Homo sapiens (human, species) [taxon 9606], Ananas ananassoides (species) [taxon 2811908], Leptospermum (genus) [taxon 106047], Anemone cathayensis (species) [taxon 2201478], Cucurbita pepo (species) [taxon 3663], Anthurium andraeanum (flamingo-lily, species) [taxon 226677], Cucumis melo var. inodorus (casaba melon, varietas) [taxon 357961], Arabidopsis thaliana (mouse-ear cress, species) [taxon 3702], Clerodendrum chinense (species) [taxon 54464], Paeonia lactiflora (Chinese peony, species) [taxon 35924], Apis mellifera (bee, species) [taxon 7460], Hemerocallis citrina (species) [taxon 1249515], Nicotiana tabacum (American tobacco, species) [taxon 4097], Prunus laurocerasus (cherry laurel, species) [taxon 32242], Liriodendron tulipifera (species) [taxon 3415], Echinacea purpurea (species) [taxon 53751], Brassica juncea (brown mustard, species) [taxon 3707], Polemonium caeruleum (species) [taxon 174663], Tococa guianensis [taxon 260122]

## Full text

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## References

88 references — full list in the complete paper: https://tomesphere.com/paper/PMC12944572/full.md

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Source: https://tomesphere.com/paper/PMC12944572