• A comprehensive review on Nymphaea stellata: A traditionally used bitter

    Type Journal Article
    Author M. K. Mohan Maruga Raja
    Author Neeraj Kumar Sethiya
    Author S. H. Mishra
    URL https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3255414/
    Volume 1
    Issue 3
    Pages 311-319
    Publication Journal of Advanced Pharmaceutical Technology & Research
    ISSN 2231-4040
    Date 2010
    Extra 00076 PMID: 22247863 PMCID: PMC3255414
    Journal Abbr J Adv Pharm Technol Res
    DOI 10.4103/0110-5558.72424
    Accessed 11/17/2021, 2:20:20 PM
    Library Catalog PubMed Central
    Abstract Nymphaea stellata Willd. (Syn. Nymphaea nouchali Burman f.) (Nymphaeaceae) is an important and well-known medicinal plant, widely used in the Ayurveda and Siddha systems of medicines for the treatment of diabetes, inflammation, liver disorders, urinary disorders, menorrhagia, blenorrhagia, menstruation problem, as an aphrodisiac, and as a bitter tonic. There seems to be an agreement between the traditional use and experimental observations, such as, hepatoprotective, anti-inflammatory, and particularly antidiabetic activity. Nymphayol, a steroid isolated from the flowers has been scientifically proved to be responsible for the traditionally claimed antidiabetic activity; it reverses the damaged endocrine tissue and stimulates secretion of insulin in the β-cells. However, taking into account the magnitude of its traditional uses, the studies conducted are still negligible. This review is an attempt to provide the pharmaceutical prospective of Nymphaea stellata.
    Short Title A comprehensive review on Nymphaea stellata
    Date Added 11/17/2021, 2:20:20 PM
    Modified 1/23/2022, 9:33:45 PM

    Tags:

    • germination
    • review
    • phytochemistry
    • cultivation

    Notes:

    • Extracted Annotations (1/23/2022, 9:33:29 PM)

      "The blue apart, and two-to-three feet apart in the rows. om seeds, but it takes three to four years to flower." (p. 313)

      "own from seeds, but it takes three to during summer. Finely sieved clean loam soil without any organic matter or fertilizer is used. Seeds should be sown thinly, covered lightly with soil and then plunged into shallow water, no deeper than 2.5 cm, and placed in a sunny position. Germination should take three-to-four weeks." (p. 313)

      "When the first two or three floating leaves appear the seedling should be picked out and planted into individual containers and immersed back in the water." (p. 313)

    Attachments

    • PubMed Central Link
    • Raja et al_2010_A comprehensive review on Nymphaea stellata.pdf
  • Analysis of Genetic Diversity and Phylogenetic Relationship in the Genus Nymphaea Using DNA Profiling

    Type Book Section
    Author Jeremy Dkhar
    URL http://hdl.handle.net/10603/5275
    Edition 1
    Place New Delhi, India
    Publisher Excel India Publishers
    Pages 105-120
    ISBN 978-93-84869-79-3
    Date October 2015
    Extra 00000
    Library Catalog Zotero
    Language en
    Abstract A comprehensive reassessment of seven Indian representatives of the genus Nymphaea viz. N. alba var. rubra, N. caerulea, N. × marliacea, N. nouchali, N. pubescens, N. rubra and N. tetragona is presented based on morphology, RAPD, PCR-RFLP and sequence data of the ITS region, chloroplast trnK intron, matK and rbcL gene in the current study. Morphological examinations revealed considerable variation among the species investigated. Of significant interest, from the context of evolutionary genetic studies, are two sympatric races of N. nouchali viz. N. nouchali JD 06 and N. nouchali JD 07, resembling each other in all aspects but showed flower colour polymorphism with blue and white coloured flowers respectively. Furthermore, members of subgenus (subg.) Lotos namely N. pubescens and N. rubra showed white coloured pollen in contrast to yellow pollen of the remaining species. Interestingly, the white coloured petals of N. pubescens exhibited a tinge of pink at the apex, resembling the petals colour of N. rubra. Barring N. caerulea and N. nouchali, RAPD analysis of randomly selected individuals from each species showed low genetic variation. The variability detected for N. caerulea may be attributed to the breeding system followed, suggesting it to be an outcrossing species. Surprisingly, no genetic variation was recorded among individuals of N. tetragona, a critically rare and endangered plant of India, necessitating its immediate conservation plan. PCR-RFLP of the ITS region revealed additional fragments, exceeding the expected size of the ITS region when totalled, in N. alba var. rubra, N. × marliacea, N. rubra and N. pubescens. Sequencing of the ITS region indicated that the extra fragments, manifested as additional signals in the sequencing chromatogram in N. pubescens may be due to random mutations occurring in some of the ITS paralogues. However, recent hybridization and introgression may be the reason for the additional signals depicted in the chromatograms of N. alba var. rubra and N. rubra. Interestingly, matK gene of N. tetragona revealed higher number of nonsynonymous substitutions. Molecular evolutionary analysis indicated that three of these sites may be under mild selective pressures. Such adaptive changes at the DNA and protein sequence level of matK gene may have been associated with the colonization of N. tetragona, suggesting that it could have migrated from China. Based on neighbour joining, maximum parsimony, maximum likelihood and Bayesian inference, phylogenetic relationship among the investigated species is presented and discussed.
    Book Title Biotechnological Approaches in Ex Situ Conservation of Plant Genetic Resources of Northeast India
    Date Added 11/17/2021, 4:21:31 PM
    Modified 4/20/2022, 8:51:55 PM

    Tags:

    • genetic

    Notes:

    • N. subgenus Anecphya, comprising 7-10 species, is restricted to Australia and New Guinea. N. subg. Brachyceras, consisting of 14-16 species, has a pantropical range, whereas N. subg. Hydrocallis, comprising 14 species, is confined to the Neotropics. N. subg. Lotos is paleotropical with 2-3 species, while N. subg. Nymphaea, comprising 8 species, occur throughout the Northern Hemisphere in temperate regions.

      The wild species found in India are N. alba, N. candida, N. nouchali, N. pubescens, N. rubra, and N. tetragona, and the cultivated species are N. alba var rubra, N. caerulea, N. micrantha, and N x maliacea.

      However, the traditional classificaiton of Nymphaea in India has been reported to be confusing with some names inaccurately used (Cook, 1996).

      Withing subg. Brachyceras, three clades were resolved by the trnT-trnF sequence data. The first clade comprised N. caerulea and N. colorate, followed by a clade comprising N. micrantha, N. heudelotti, and N. thermarum, and another clade comprising N. ampla, N. elegans and N. gracilis.

      Barring N. caerulea and N. nouchali, RAPD analysis of randomly selected individuals from each species showed low or no genetic variation at both inter- and intra- populations levels (Fig. 7.3). The variability detected for N. caerulea might possible be due to high rate of cross-pollination among individuals of N. caerulea. In N. nouchali, considerable morphological variation accounted for the high genetic variability (68.09%).

      Within subg. Brachyceras, represented here by two species i.e. N. caerulea and three specimins of N. nouchali, incongruence exist between chloroplast and nuclear marker for the phylogenetic placement of N. nouchali JD 02. All chloroplast markers support the association of N. nouchali JS 02 with N. caerulea whereas the ITS data showed it to be closer to the remaining specimen of N. nouchali. Molecular evidence provided here is in disagreement about the taxonomic identity of N. nouchali JD 02.

      Molecular evidence provided is in disagreement about the taxonomic identity of one specimen of N. nouchali and indicated a probable misidentification of N. tetragona.

      The name N. nouchali was initially applied to two specimens, viz., N. nouchali JS 02 and N. nouchali JS 06. The two specimens were found to be morphologically dissimilar and showed variability in texture (thick/thin), mottling and veins (impressed/raised) of the leaf, and number of petals and stamens. In the present study, sequence analysis of matK and trnK altogether revealed 7 substitutions among the two samples and a repeat motif GGGC was found in the trnK sequence of N. nouchali JS 06. Analysis of complete ITS sequences recorded 5 substitutions between them and 2 deletions (CAA and A) in N. nouchali JS 06. Such variations suggested distinctness between the two specimens and a probably identity of N. nouchali JS 02 as N. capensis (nucleotide BLAST of the ITS region of N. nouchali JS 02 showed 99.13% sequence identity with N. capensis, Accession no. AY707898). However, N. capensis has never been reported from India.

      The results indicated no close association between N. petersiana and N. nouchali, thereby, contradicting the morphology-placed treatment of placing N. petersiana in synonymy under N. capensis and N. nouchali, respectively.

    Attachments

    • Dkhar_Analysis of Genetic Diversity and Phylogenetic Relationship in the Genus.pdf
  • Characterization of Cadmium Uptake by the Water Lily Nymphaea aurora

    Type Journal Article
    Author Tamar Schor-Fumbarov
    Author Zvika Keilin
    Author Elisha Tel-Or
    URL https://doi.org/10.1080/713610178
    Volume 5
    Issue 2
    Pages 169-179
    Publication International Journal of Phytoremediation
    ISSN 1522-6514
    Date April 1, 2003
    Extra 00000 Publisher: Taylor & Francis _eprint: https://doi.org/10.1080/713610178 PMID: 12929498
    DOI 10.1080/713610178
    Accessed 11/17/2021, 2:53:38 PM
    Library Catalog Taylor and Francis+NEJM
    Abstract This study characterizes cadmium (Cd) uptake by the waterlily Nymphaea aurora, (Nymphaeaceae) in two systems: a model hydroponic Cd solution and heavily polluted sludge from two sites in Israel. The uptake of Cd from hydroponic solution resulted in Cd storage in petioles and laminae of Nymphaea, as well as in the roots. The pH of the solution affected Cd solubility and availability, with pH 5.5 yielding maximum Cd content in the plant (140 mg Cd per g DW). Cd uptake was reduced by the addition of EDTA to the hydroponic growth medium, although EDTA enhanced heavy metal uptake by terrestrial plants. Nymphaea efficiently reduced the concentration of Cd in heavy metal polluted urban and industrial sludge and the amount of Cd uptake was enhanced by the addition of KCl to the sludge and by adjustment of the pH to 5.5. The inherent growth patterns of Nymphaea plants allowed Cd uptake by the shoot and root, and resulted in maximum contact between the various plant parts and the growth media. Thus, Nymphaea has potential as an optimal, highly effective phytoremediation tool for the removal of Cd from polluted waste sources.
    Date Added 11/17/2021, 2:53:38 PM
    Modified 11/17/2021, 2:53:39 PM

    Tags:

    • cadmium
    • hydroponics
    • industrial sludge
    • Nymphaea (waterlily)
    • phytoremediation
    • urban sludge.

    Notes:

    • Extracted Annotations (1/24/2022, 12:06:11 AM)

      "For the hydroponic protocols, each explant (tissue that has been taken from a plant and placed in a culture medium) containing regeneration buds was planted in an individual pot (5 cm diameter, 7 cm height) containing gravel medium and tap water." (p. 172)

      "Three weeks post planting, each pot was placed in a larger white pot (20-cm-diameter base, 22-cm-diameter apex, 20 cm height), containing tapwater (pH ~6.7)." (p. 172)

      "Control plants were grown in tap water (pH 6.7) without supplements." (p. 172)

      "Industrial sludge from Kibbutz Givat-Brener containing approximately 400 to 450 mg/kg Cd and urban sludge from Haifa Bay containing ~100 mg/kg Cd were used in the sludge experiments. Heavy clay soil from Kibbutz Hazorea was employed in the control experiments. The clay soil represented the natural growth medium of the Nymphaea prior to transplanting into the experimental media." (p. 172)

      "Plants were potted in 50 L containers with the selective media and sampled at intervals of 28, 68, and 91 days (Figure 4) or after 5 weeks (Figure 5)." (p. 172)

      "Necrotic spots were observed on the laminae of treated plants and their development was obviously retarded when compared with the control plants." (p. 173)

    Attachments

    • Schor-Fumbarov et al_2003_Characterization of Cadmium Uptake by the Water Lily Nymphaea aurora.pdf
    • Snapshot
  • Comparative phytochemical analysis of four Mexican Nymphaea species

    Type Journal Article
    Author Silvia Marquina
    Author Jaime Bonilla-Barbosa
    Author Laura Alvarez
    URL https://www.sciencedirect.com/science/article/pii/S0031942205000919
    Volume 66
    Issue 8
    Pages 921-927
    Publication Phytochemistry
    ISSN 0031-9422
    Date April 1, 2005
    Extra 00028 tex.ids= marquina_comparative_2005-1
    Journal Abbr Phytochemistry
    DOI 10.1016/j.phytochem.2005.02.027
    Accessed 11/17/2021, 8:00:23 PM
    Library Catalog ScienceDirect
    Language en
    Abstract Four Mexican Nymphaea species, N. ampla, N. pulchella, N. gracilis and N. elegans belonging to subgenera Brachyceras were analyzed. In this work two 5-glycosyl isoflavones, 7,3′,4′-trihydroxy-5-O-β-d-(2″-acetyl)-xylopyranosylisoflavone (1) and 7,3′,4′-trihydroxy-5-O-α-l-rhamnopyranosylisoflavone (2), were isolated from N. ampla and N. pulchella, respectively, together with other known 3-glycosyl flavones and triterpene saponins from the same four species. The structures were elucidated by 1D and 2D NMR, FABMS, and other spectroscopic analyses. These results confirmed that the four species were different from each other and established that N. pulchella represents a different taxa than N. ampla. In addition, the 5-glycosyl isoflavones could be considered as a taxonomic character of this group of plants.
    Date Added 11/17/2021, 8:00:23 PM
    Modified 3/17/2022, 4:26:01 PM

    Tags:

    • Nymphaeaceae
    • 5-glycosyl isoflavones
    • Taxonomic character

    Notes:

    • Contents

      • Introduction
      • Results and discussion
      • Experimental
        • General experimental procedures
        • Plant material
        • Extraction and isolation
        • 7,3 prime ,4 prime ,Trihydroxy-5-O- beta -d-(2 Prime -acetyl) xylopyranosylisoflavone (1)
        • Acid hydrolysis of compound 1
        • 7,3 prime ,4 prime -Trihydroxy-5-O- alpha -l-rhamnopyranosylisoflavone (2)
      • Acknowledgements
      • References

    Attachments

    • Marquina et al_2005_Comparative phytochemical analysis of four Mexican Nymphaea species.pdf

      Contents

      • Introduction
      • Results and discussion
      • Experimental
        • General experimental procedures
        • Plant material
        • Extraction and isolation
        • 7,3 prime ,4 prime ,Trihydroxy-5-O- beta -d-(2 Prime -acetyl) xylopyranosylisoflavone (1)
        • Acid hydrolysis of compound 1
        • 7,3 prime ,4 prime -Trihydroxy-5-O- alpha -l-rhamnopyranosylisoflavone (2)
      • Acknowledgements
      • References
    • ScienceDirect Snapshot
  • Effect of Pot Size on Plant Growth and Multiplication of Water Lilies (Nymphaea sp)

    Type Journal Article
    Author H S Al-Menaie
    Author O Al-Ragam
    Author N Al-Dosery
    Author M Zalzaleh
    Author M Mathew
    Author N Suresh
    Volume 12
    Issue 2
    Pages 148-153
    Publication Environ. Sci.
    Date 2012
    Extra 00009
    Library Catalog Zotero
    Language en
    Abstract Growth performance and multiplication of two promising water-lily varieties (Nymphaea sp.) namely, N. rosea and N. sunrise were studied at the Urban Demonstration Garden Site (UDG) of Kuwait Institute for Scientific Research (KISR), using different types of pots. Three replicates of each variety were tested using pots of three different sizes i.e., 29 h x 30 w x 29 d cm (circular), 50 h x 45 w x 22 d cm (rectangular) and 22 h x 22 w x 13 d cm (baskets) in split plot design. The water lilies were planted in containers filled with a growing medium of sand: sphagnum peat moss in 2:1 (v/v) and then placed in tanks filled with fresh water. Growth rate was measured on a monthly basis through the petiole length, leaf width, number of leaves and number of flowers. At the end of the study, observations on the number of the offshoots, buds and seedlings produced from each plant were recorded to study the effect of pot size on water-plant growth. Among the three different sized pots studied, rectangular pots of size 50 h x 45 w x 22 d cm were found to be the best for the growth and multiplication of N. rosea and N. sunrise. This could be due to the increased plant-leaf area, shoot biomass and root biomass in rectangular pots compared to circular pots and baskets.
    Date Added 11/17/2021, 2:50:43 PM
    Modified 11/17/2021, 2:51:24 PM

    Notes:

    • Extracted Annotations (1/18/2022, 11:24:33 PM)

      "The performance of these varieties was evaluated under the climatic conditions of Kuwait. Among these varieties, two promising varieties namely N. rosea andN. sunrise were selected to determine the effect of pot size on water-plant growth and multiplication." (p. 149)

      "Pots of three different sizes i.e., 29 h x 30 w x 29 d cm (circular), 50 h x 45 w x 22 d cm (rectangular) and 22 h x 22 w x 13 d cm (baskets) were filled with a growing medium of sand: sphagnum peat moss in 2:1 (v/v) and the containers were thoroughly soaked for compacting." (p. 149)

      "Once the plants were established, aquatic fertilizer tablets were inserted in the growing medium about two inches from the rhizome." (p. 149)

      "Flowers fade after about three to five days; and leaves last for a few weeks and then fade away." (p. 149)

      "For optimum growth of water plants, the pond water should have a neutral or slightly alkaline pH (in the range of 7 to 8)." (p. 149)

      "In order to maintain an optimum pH in the pond, care was taken to cover only 50-70% of the water surface with the plants." (p. 149)

      "Routine removal of sludge and decaying organic matter was carried out to maintain optimum pH." (p. 149)

      "The top portion of the containers was filled with one inch of sand to prevent the top soil from discoloring the pond water." (p. 149)

      "Rectangular pots of size 50 h x 45 w x 22 d cm were found to be the best for the growth and multiplication of N. rosea and N. sunrise. This could be due to the increased plant-leaf area, shoot biomass and root biomass in rectangular pots compared to circular pots and baskets." (p. 152)

      "When the container size was reduced, the rooting volume decreased leading to a reduction in plant growth." (p. 152)

      "Plant growth was stunted even for the best performing plants, due to the small pot size [9]." (p. 152)

    Attachments

    • Al-Menaie et al_2012_Effect of Pot Size on Plant Growth and Multiplication of Water Lilies (Nymphaea.pdf
  • Expression and Functional Analyses of Nymphaea caerulea MADS-Box Genes Contribute to Clarify the Complex Flower Patterning of Water Lilies

    Type Journal Article
    Author Silvia Moschin
    Author Sebastiano Nigris
    Author Ignacio Ezquer
    Author Simona Masiero
    Author Stefano Cagnin
    Author Enrico Cortese
    Author Lucia Colombo
    Author Giorgio Casadoro
    Author Barbara Baldan
    URL https://www.frontiersin.org/article/10.3389/fpls.2021.730270
    Volume 12
    Pages 2018
    Publication Frontiers in Plant Science
    ISSN 1664-462X
    Date 2021
    Extra 00000
    DOI 10.3389/fpls.2021.730270
    Accessed 12/4/2021, 8:36:42 PM
    Library Catalog Frontiers
    Abstract Nymphaeaceae are early diverging angiosperms with large flowers characterized by showy petals and stamens not clearly whorled but presenting a gradual morphological transition from the outer elements to the inner stamens. Such flower structure makes these plant species relevant for studying flower evolution. MADS-domain transcription factors are crucial components of the molecular network that controls flower development. We therefore isolated and characterized MADS-box genes from the water lily Nymphaea caerulea. RNA-seq experiments on floral buds have been performed to obtain the transcript sequences of floral organ identity MADS-box genes. Maximum Likelihood phylogenetic analyses confirmed their belonging to specific MADS-box gene subfamilies. Their expression was quantified by RT-qPCR in all floral organs at two stages of development. Protein interactions among these transcription factors were investigated by yeast-two-hybrid assays. We found especially interesting the involvement of two different AGAMOUS-like genes (NycAG1 and NycAG2) in the water lily floral components. They were therefore functionally characterized by complementing Arabidopsis ag and shp1 shp2 mutants. The expression analysis of MADS-box genes across flower development in N. caerulea described a complex scenario made of numerous genes in numerous floral components. Their expression profiles in some cases were in line with what was expected from the ABC model of flower development and its extensions, while in other cases presented new and interesting gene expression patterns, as for instance the involvement of NycAGL6 and NycFL. Although sharing a high level of sequence similarity, the two AGAMOUS-like genes NycAG1 and NycAG2 could have undergone subfunctionalization or neofunctionalization, as only one of them could partially restore the euAG function in Arabidopsis ag-3 mutants. The hereby illustrated N. caerulea MADS-box gene expression pattern might mirror the morphological transition from the outer to the inner floral organs, and the presence of transition organs such as the petaloid stamens. This study is intended to broaden knowledge on the role and evolution of floral organ identity genes and the genetic mechanisms causing biodiversity in angiosperm flowers.
    Date Added 12/4/2021, 8:36:42 PM
    Modified 4/6/2022, 5:45:43 PM

    Tags:

    • genetic
    • description

    Notes:

    • Extracted Annotations (1/19/2022, 1:16:39 AM)

      "The hermaphroditic flower of N. caerulea arises above the water surface one day before anthesis thanks to the growth of the petiole. Like most of water lily flowers, this flower is protogynous with a diurnal opening." (p. 2022)

      "The first day of anthesis stamens are in a vertical position (Figure 1A), facilitating the access of pollinators" (p. 2022)

      "to the exposed pistil, which is surrounded by a stigmatic fluid that attracts insects (Schneider and Chaney, 1981); during the first day of anthesis, the flower is thus prepared to receive pollen from other flowers. From the day after, the flower keeps the stamens in an oblique position, concealing almost completely the stigma (Figure 1B). Therefore, pollinators must go across stamens to reach the nectar, covering themselves with the pollen produced by the mature male organs. This mechanism promotes crossfertilization. N. caerulea floral organs are shown in Figure 1." (p. 2023)

    Attachments

    • Moschin et al_2021_Expression and Functional Analyses of Nymphaea caerulea MADS-Box Genes.pdf

      Contents

      • Introduction
      • Materials and Methods
        • Nymphaea caerulea Material, RNA Extraction, Quantification, and Cleaning
        • Pollen Viability Assay
        • Transcripts Isolation and Identification
        • Amplification by RT-PCR of NycAP3 Isoforms
        • Gene Expression Analysis by RT-qPCR
        • Phylogenetic Analysis
        • Yeast Two-Hybrid Assays
        • Constructs and Arabidopsis Plant Transformation
        • Fixation, Clearing, and Phloroglucinol Staining of Arabidopsis Fruits
        • Quantification of NycAGs Expression in Arabidopsis Transformed Lines by RT-qPCR
      • Results
        • The Flower Structures of Nymphaea caerulea
        • MADS-Box Genes Isolated in Nymphaea caerulea Developing Flowers
        • Analysis of MADS-Box Gene Expression in the Flower Organs of N. caerulea
        • Analysis of MADS-Domain Protein–Protein Interactions by Yeast Two-Hybrid Assays
        • Functional Analysis of NycAG1 and NycAG2 by Complementation Experiments With Arabidopsis ag and shp1 shp2 Mutants
      • Discussion
        • The Array of MADS-Box Genes in the Flower of Nymphaea caerulea
        • The AGAMOUS Subfamily in Nymphaea caerulea
        • Protein–Protein Specific Interactions Between MADS-Box of Nymphaea caerulea
      • Conclusion
      • Data Availability Statement
      • Author Contributions
      • Funding
      • Acknowledgments
      • Supplementary Material
      • References
  • Factors Affecting Germination of Seeds of Fragrant Waterlily (Nymphaea odorata)

    Type Journal Article
    Author Mary Jane Else
    Author Donald N. Riemer
    URL https://www.apms.org/wp/wp-content/uploads/2012/10/v22p22.pdf
    Volume 22
    Pages 22-25
    Publication Journal of Aquatic Plant Management
    Date 1984
    Extra 00000
    Abstract Fragrant waterlily (Nymphaea odorata Ait.) is an aquatic weed of wide distribution. Seeds from weed populations in souther New Jersey were studied to determine germination requirements. Seeds were dormant at time of release and no after-ripening requirement was observed. Mechanical puncturing of the seed coat had no effect upon germination. Seeds germinated when large numbers were crowded in a small container, and it was thought that the seeds themselved produced something that promoted their germination. Promotion of germination by 2-chloroethylphosphonic acid (ethephon) and inhibition of germination by aeration and CO2 suggested that this substance was ethylene gas in solution. Germination under conditions of seed crowding was inhibited by darkness and promoted by stratification. Stratification at 4.4C for 5 months resulted in germination of crowded seeds in excess of 90%. Germination was strongly inhibited by periods of freezing or drying as short as 1 day.
    Date Added 11/17/2021, 2:39:54 PM
    Modified 1/23/2022, 9:07:24 PM

    Tags:

    • germination

    Notes:

    • After the seeds had become free of their surrounding arils they were stored in fresh water on a laboratory bench at room temperature with alternating 12 hour periods of light and darkness.

      All germination experiments were conducted in 35 ml glass vials measuring approximately 2.5 cm in diameter and 10.5 cm in height.

      Seeds were counted and placed in these vials with either 20 or 25 ml tap water, depending on the experiment.

      In initial experiments, seeds collected in 1978 failed to germinate when small numbers were placed in petri dishes. Extra seeds which were left in a crowded condition in a glass dish on a laboratory bench, did germinate, however, at a rate of approximately 50%.

      Experiment 6... Seeds were stored in the dark at 4.4C for the indicated time.

      Experiment 7. In this experiment, fragrant waterlily seeds were air-dried for 0, 1, 3, 10, 24, 58, and 96 hours.

      In three seasons of experimental work not a single fragrant waterlily seed germinated when the number of seeds per vial was 20 or less.

      Germination did not increase with time, indicating that there is no after-ripening requirement. Approximately 60% of the seeds rotted after a year's storage in water at room temperature.

      Germination increased significantly with increasing concentrations of seeds, starting at 60 seeds/vial and reaching a maximum at 100 seeds/vial. Densities greater than 100 seeds/vial (5 seeds/ml) had no further effect on germination.

      Transfer of water from a container of actively germinating seeds to a container of uncrowded seeds which were not germinating initiated germination in the uncrowded seeds.

      All gas treatments of crowded seeds resulted in significant decreases in germination compared to untreated controls.

      Treatment with ethephon stimulated germination in all cases when: the ethephon concentration was 1.0 ppm or more in the uncrowded seeds and 0.01 ppm or more in the crowded seeds.

      Few germination percentages exceeded 20% in [experiment 4], which is lower than those which occurred in the other experiments. It is possible that the tight vial closure, necessary in this experiment to keep the ethylene gas from escaping, resulted in the buildup of toxic respiratory products or products  antagonistic to the function of ethylene.

      Seeds kept in the dark exhibited only 2% germination, even when crowded, while seeds kept in the light exhibited nearly 30% germination.

      Early experiments indicated that fragrant waterlily seeds do not respond to stratification periods of 9 weeks or less.

      Stratification for 7 and 9 months enhanced germination percentages to nearly 100% in the crowded containers.

      A drying time of only 3 hours resulted in significant inhibition of germination and the percentage declined rapidly up to drying times of 24 hours.

      Four days of freezing resulted in germination of only 4.9%, and one week of freezing prevented germination entirely.

      Mechanical rupture of seed coats failed to induce germination in fragrant waterlily.

    Attachments

    • Else_Riemer_1984_Factors Affecting Germination of Seeds of Fragrant Waterlily (Nymphaea odorata).pdf

      Contents

  • Flavonoids from blue flowers of Nymphaèa caerulea

    Type Journal Article
    Author Torgils Fossen
    Author Åsmund Larsen
    Author Bernard T Kiremire
    Author Øyvind M Andersen
    URL https://www.sciencedirect.com/science/article/pii/S0031942299000497
    Volume 51
    Issue 8
    Pages 1133-1137
    Publication Phytochemistry
    ISSN 0031-9422
    Date August 1, 1999
    Extra 00000
    Journal Abbr Phytochemistry
    DOI 10.1016/S0031-9422(99)00049-7
    Accessed 11/17/2021, 10:06:25 PM
    Library Catalog ScienceDirect
    Language en
    Abstract Seven flavonols including the novel 3-(2″-acetylrhamnosides) of myricetin and quercetin (2 and 6), the rare kaempferol 3-(2″-acetylrhamnoside) and quercetin 3-(3″-acetylrhamnoside), in addition to the 3-rhamnosides of kaempferol, quercetin and were isolated from blue flowers of the African water lily Nymphaèa caerulea (=Nymphaèa capensis). Their structures were elucidated by a combination of chromatography and homo- and heteronuclear two-dimensional NMR techniques and electrospray MS for compound 2.
    Date Added 11/17/2021, 10:06:25 PM
    Modified 1/23/2022, 11:55:27 PM

    Tags:

    • phytochemistry
    • Flavonol 3-rhamnosides
    • Kaempferol 3-(2″-acetylrhamnoside)
    • Myricetin 3-(2″-acetylrhamnoside)
    • Nymphaèaceae
    • Quercetin 3-(2″-acetylrhamnoside)
    • Quercetin 3-(3″-acetylrhamnoside)
    • Water lily

    Notes:

    • Annotations
      (4/6/2022, 5:55:31 PM)

      “It is interesting to note that all the isolated Øavonols, 1±7, from the blue Øowers of N. caerulea have a rhamnosyl moiety in the aglycone 3-position, while all the Øavonols which were isolated from the red petals of N. marliacea were Øavonol 3'-xylosides (Fossen et al., 1998a).” (Fossen et al., 1999, p. 1136)

      “In contrast to this, red Øowers of this latter species have anthocyanins with galactosyl moieties in the 3-position (Fossen et al., 1998b), while the blue Øowers of N. caerulea contain analogous anthocyanins with galactosyl moieties in the 3 '-position.” (Fossen et al., 1999, p. 1136)

      “Flowers (500 g) of the African water lily N. caerulea (=N. capensis ) were collected in September 1997 from Wamiko water pond, west of Kampala, Uganda.” (Fossen et al., 1999, p. 1136)

    Attachments

    • Fossen et al_1999_Flavonoids from blue flowers of Nymphaea caerulea.pdf
    • ScienceDirect Snapshot
  • Germination and early growth of Nymphaea odorata at different water depths

    Type Journal Article
    Author Jennifer H. Richards
    Author Carla Cao
    URL https://www.sciencedirect.com/science/article/pii/S0304377011001768
    Volume 98
    Issue 1
    Pages 12-19
    Publication Aquatic Botany
    ISSN 0304-3770
    Date April 1, 2012
    Extra 00018
    Journal Abbr Aquatic Botany
    DOI 10.1016/j.aquabot.2011.12.003
    Accessed 11/17/2021, 2:26:34 PM
    Library Catalog ScienceDirect
    Language en
    Abstract We experimentally determined the effects of water depth on seed germination and seedling growth and morphology, and we documented the transition from submerged to emergent plants in the white water lily, Nymphaea odorata. Seeds of N. odorata were germinated at 30, 60, and 90cm water depth in outdoor mesocosms and percent germination and morphology measured after a month. The presence of self-seeded seedlings in pots at the same 3 water levels was also recorded over two years. To examine juvenile growth, seeds planted in soil were placed at the same mesocosm depths; germination and growth were monitored for three months, when the plants were harvested for morphological and biomass measurements. N. odorata germinated equally well in 30, 60 and 90cm water; seedlings grew as submerged aquatics. After one month, seedlings in 90cm water had less biomass than those in 30cm (1.1 vs. 3.3mg and 1.0 vs. 1.8mg for different seed sources, respectively) and allocated relatively more biomass to shoots (97.5 vs. 67.8% and 73.1 vs. 58.0%, respectively). Seedlings in 60cm water were intermediate. After 3 months of submerged growth, plant biomass remained less in 90 vs. 60 and 30cm water (22.5 vs. 36.4 and 33.3mg, respectively). Plants in 90 and 60cm water had greater biomass allocation to shoots than plants in 30cm water (85.7 and 72.6% vs. 64.4%, respectively) and produced larger laminae on longer petioles (lamina length=33.3 vs. 25.2mm in 90 vs. 30cm; petiole length=99.0 vs. 36.0mm, respectively). After about 3 months, submerged plants produced floating leaves that had 39% shorter laminae but 267% to 1988% longer petioles than submerged leaves on the same plant. Lamina length to width allometric relations of submerged leaves were >1 at all water levels, distinguishing them from the equal allometry of adult floating leaves. The switch from production of submerged to emergent leaves resembles submergence-escape growth in other aquatics, but because the seedlings have been submerged throughout their life, submergence itself cannot be the stimulus to produce emergent leaves in these totally immersed plants. Our data show that N. odorata plants can establish from seeds in up to 90cm water and that seedlings grow as submerged aquatics until they switch abruptly to production of floating leaves.
    Date Added 11/17/2021, 2:26:34 PM
    Modified 1/23/2022, 9:07:24 PM

    Tags:

    • germination
    • Seedling growth
    • Seed germination
    • Nymphaeaceae
    • Freshwater aquatic plant
    • Juvenile growth
    • LOES
    • Low oxygen escape syndrome
    • Submergence-escape
    • Water depth

    Notes:

    • Extracted Annotations (1/18/2022, 11:24:06 PM)

      "In both sets of experiments we germinated seeds in 25 ml glass vials placed at 30, 60 and 90 cm water depths in the mesocosms. Vials had no added soil, so seeds germinated and grew for a month in water. Vials were covered with plastic screening to retain the seeds but allow water and gas exchange." (p. 13)

      "The mesocosms were 3410 L (900 gal) round polypropylene cattle tanks that were 1 m deep × 2.1 m wide. Plants were grown in native peat in 25 cm diameter × 19 cm high pots on shelves suspended at 30 and 60 cm depths with an additional shelf on the" (p. 13)

      "bottom at 90 cm depth." (p. 13)

      "In order to examine the effects of water on germination and the earliest stages of seedling growth, we assayed germination in glass vials suspended at different depths in the mesocosms." (p. 13)

      "The MG seed germination trials were conducted from September through December 2010, as seeds became available. Seeds were collected within a day of fruit dehiscence and were exposed to sunlight for at least 5 h while floating in water-filled containers. After exposure, 10 seeds were placed in each vial, and five vials were placed at each water level in a mesocosm." (p. 13)

      "rea 3B (25e placed in beakers set in water in the mesocosm area; one fruit dehisced on June 9 2011, and the seeds were exposed to sunlight for a day, then were placed in glass vials suspended individually at 30, 60 and 90 cm water levels in two mesocosms (n = 7 vials per water level per mesocosm); vials at different water depths were interspersed." (p. 13)

      "In 2009 seeds were planted in 12 cm × 8 cm plastic inserts filled with commercial potting soil; each insert had six 4 cm × 4 cm subdivisions. Four seeds were planted per subdivision, resulting in 24 seeds per insert. We placed seeds from a single fruit in three inserts, and each insert was placed at one of three water depths (30, 60 and 90 cm) in a mesocosm." (p. 14)

      "To further document this phenomenon, in June 2010 we planted germinated seedlings at 30, 60 and 90 cm water depths in three mesocosms and monitored production of floating leaves over the next three months." (p. 14)

      "During the FG germination experiment from June 9 to July 11 2011, air temperature on the FIU campus averaged 27.6 ± 2.4 ◦ C (range = 21.9-35.8 ◦ C), while day length varied from 13 h 38 m to 13 h 45 m. The pH of the tanks averaged 7.08 ± 0.41, conductivity was 225.5 ± 12.4, and total dissolved solids were 448 ± 25." (p. 15)

      "photosynthetically active radiation (PAR) at 30 cm was 42.6 ± 2.4% of surface irradiance; PAR at 60 cm was 27.6 ± 1.9%; and PAR at 90 cm was 19.4 ± 1.7%." (p. 15)

      "In the simplified model seedling number did not differ significantly among water depths but did differ significantly among maternal genotypes: removing water depth did not produce a significantly different model (2 = 0.84, df = 2, Pr > 2 = 0.6570), but removing genotype did (2 = 36.88, df = 5, Pr > 2 < 0.0001)." (p. 15)

      "Percent germination from the June 2011 FG seeds was very high, ranging from 99% to 100% (30 cm = 99 ± 4%, 60 cm = 99 ± 3%, 90 cm = 100%) with no significant differences between tanks (Pr > 2 = 0.3561, GLM) or among water levels (Pr > 2 = 0.8030, GLM) and no significant interactions (Pr > 2 = 0.8106, GLM)." (p. 15)

      "Percent germination for the MG seeds in September through December 2010 was more variable, ranging from 57% to 91% averages in individual trials (30 cm = 68 ± 4%; 60 cm = 81 ± 3%; 90 cm = 77 ± 4%). There were significant differences among trials (Pr > 2 < 0.0001, GLM), among water levels (Pr > 2 = 0.0015, GLM) and significant interactions (Pr > 2 < 0.0001, GLM)." (p. 15)

      "The significant differences in germination among water levels were between 30 cm water and the other two water levels, with germination at 30 cm being less in four of the five trials." (p. 15)

      "After a month, FG seedlings had matured 2 leaves (median; range = 0-4). Forty-four percent of FG seedlings at 30 cm water depth had deltoid laminae, compared to 31% at 60 cm and 12% at 90 cm." (p. 15)

      "In the 2009 experiment after about 3 months of submerged growth, juvenile plants at all water levels had 3 (range = 0-7)" (p. 16)

      "mature leaves present, but leaf morphology differed among plants at different water levels (Table 1B)." (p. 16)

      "Submerged juvenile plants began to produce floating laminae after about 3 months of growth." (p. 17)

      "The difference in germination percentages in our experiments when seeds were exposed to sunlight vs. when they were not suggests that sunlight greatly promotes germination." (p. 18)

    Attachments

    • Richards_Cao_2012_Germination and early growth of Nymphaea odorata at different water depths.pdf

      Contents

      • 1 Introduction
      • 2 Materials and methods
        • 2.1 Pollination and seed collection
        • 2.2 Germination and early seedling growth
        • 2.3 Submerged seedling and juvenile plant growth
        • 2.4 Transition from submerged to floating-leaved aquatic
        • 2.5 Statistical analyses
      • 3 Results
        • 3.1 Tank environment
        • 3.2 Seed germination and seedling mortality
        • 3.3 Seedling and juvenile morphology and biomass
          • 3.3.1 Seedling plants
          • 3.3.2 Juvenile plants
        • 3.4 Transition to floating-leaved plants
      • 4 Discussion
        • 4.1 Seed germination and seedling growth
        • 4.2 Seedling and juvenile morphology and growth
      • Acknowledgments
      • References
    • ScienceDirect Snapshot
  • In Vitro culture of Nymphaea nouchali seeds; a conservation approach for a vulnerable species

    Type Journal Article
    Author P. I. P. Perera
    Author T. Attanayaka
    Author K. Yakandawala
    Author D. Yakandawala
    Author C. Fernando
    Author U. Arachchi
    Author D. Gunawardhana
    Author C. Weerasinghe
    URL http://jnsfsl.sljol.info/articles/abstract/10305/
    Rights Authors who publish with this journal agree to the following terms: Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution License that allows others to share the work with an acknowledgement of the work's authorship and initial publication in this journal. Authors are able to enter into separate, additional contractual arrangements for the non-exclusive distribution of the journal's published version of the work (e.g., post it to an institutional repository or publish it in a book), with an acknowledgement of its initial publication in this journal. Authors are permitted and encouraged to post their work online (e.g., in institutional repositories or on their website) prior to and during the submission process, as it can lead to productive exchanges, as well as earlier and greater citation of published work (See The Effect of Open Access ). All third-party images reproduced on this journal are shared under Educational Fair Use. For more information on Educational Fair Use , please see this useful checklist prepared by Columbia University Libraries . All copyright of third-party content posted here for research purposes belongs to its original owners. Unless otherwise stated all references to characters and comic art presented on this journal are ©, ® or ™ of their respective owners. No challenge to any owner’s rights is intended or should be inferred.
    Volume 49
    Issue 3
    Publication Journal of the National Science Foundation of Sri Lanka
    ISSN 2362-0161
    Date 2021-09-30
    Extra 00000 Number: 3 Publisher: National Science Foundation of Sri Lanka
    DOI 10.4038/jnsfsr.v49i3.10305
    Accessed 11/17/2021, 2:16:20 PM
    Library Catalog jnsfsl.sljol.info
    Language eng
    Abstract Nymphaea nouchali var. nouchali is a non-viviparous species with a slow natural propagation by rhizomes or seeds. The plant is threatened in its natural habitats due to several reasons and included in the vulnerable category of the National Red List of Sri Lanka. In vitro contamination free culture method was developed to initiate mass propagation of the species. Results were validated through molecular and microscopic studies. Bacterial growth occurred in the seeds disinfected via standard method of using CloroxTM. Mature seeds scarified with 75 % H2SO4 for 60 seconds gave contamination free cultures with optimum seed germination. Scanning electron micrographs of mature seeds showed the rows containing trichomes running between the two poles of seeds and the sclereids between the rows of trichomes to be the potential habitats for bacteria. Light micrographs showed the thick seed coat that causes a physical dormancy. Sulphuric acid treatment was effective in degrading the trichomes completely and the seed coat partially. The highest seed germination (65.5 %) was obtained by culturing the seeds treated with 75 % H2SO4 on the solidified MS medium. The basal stem of the well-grown seedlings in vitro gave rise to the mini-rhizomes. Molecular analysis showed the close genetic relatedness within and among the isolated plant populations from where the seeds were collected. The in vitro protocol developed in this study can be used for propagation of seedlings of this vulnerable species for maintaining the biodiversity by population enhancement through restoration and introduction into new habitats.
    Date Added 11/17/2021, 2:16:20 PM
    Modified 1/23/2022, 9:08:05 PM

    Tags:

    • in vitro
    • germination

    Notes:

    • Extracted Annotations (12/24/2021, 6:33:32 PM)

      "of Sri Lanka (Dassanayake, 1996;s Guruge et al., 2016). itats due to anthropogenic activities, drying of waterbodies and the competition posed by the viviparous Nymphaea × erangae for habitats, resulting in whipping off some populations completely (Yakandawala & Yakandawala, 2011; Yakandawala et al., 2017)." (p. 2)

      "Evidence for natural hybridization among Nymphaea species has been reported elsewhere in the world, where different karyotypes ranging from 2n = 28 to 84 has been observed, generating uncertainty in species identification (Raja et al., 2010; Nierbauer et al., 2014)." (p. 2)

      "leaf explants of Nymphaea at different maturity stages. ng somatic embryogenesis in the leaf explants of N. nouchali were not successful in demonstrating the recalcitrance of this non-viviparous species." (p. 2)

      "Mature pods of N. nouchali were collected from the plant populations existing in natural habitats of marshy lands in Sri Lanka, after careful observation for the unique morphological characters in the petals, stamens, stigmatic heads, and leaf lamina of the species, as described by Yakandawala & Yakandawala (2011) and Guruge et al. (2017)." (p. 2)

      "awala & Yakandawala (2011) and Guruge et al. (2017). e soaked for three days to facilitate sedimentation of seeds by fermenting the outer pulp. After removing the debris, the seeds were isolated and washed thoroughly with soap water, followed by tap water for 30 min." (p. 2)

      "Murashige and Skoog medium (1962), supplemented with 20.0 g/L sucrose and 100.0 mg/L Myo-Inositol (w/v), was used as the basal culture medium unless otherwise mentioned. The pH was adjusted to 5.8. Solidified media with agar (6.0 g/L; w/v) were used unless otherwise mentioned." (p. 2)

      "15 Pa for 15 min (HVP 50, Hirayama, Saitama, Japan). ture medium were used for inoculating the seeds." (p. 2)

      "L ofe culture medium were used for inoculating the seeds. t 28 °C in light supplied with" (p. 2)

      "Seeds treated with 70% ethanol for 1 min were subjected to ten sterilisation protocols with five Clorox™ concentrations; 10, 30, 50, 70 or 100 % (v/v), each with two exposure times, 10- or 20-min." (p. 3)

      "After disinfecting with 70 % ethanol for 1 min and 10 % Clorox™ for 10 min, seeds were treated with five concentrations of H2SO4, 10, 25, 50, 75, and 100 % (v/v) for five exposure times 15, 30, 60, 90, 180 s." (p. 3)

      "Sixty microliters of Tween were used as the surfactant in the Clorox™ solution. After treating with each disinfectant, the seeds were washed thoroughly with distilled water three times by agitating each for 2 min." (p. 3)

      "ere treated with 25, 50 and 75 % (v/v) H2SO4 for 1 min. 2, 4-D and 2 mg/L BAP solidified with 6.0 g/L agar, the same medium in liquid form and the Albert's solution (2.22 g/L), were tested for seed germination." (p. 3)

      "Results indicated that 70 % ethanol and Clorox™ at any concentration is not sufficient for disinfection of seeds, leaving some bacteria in the hidden habitats of the seed surface." (p. 4)

      "ed and subsequently contaminated the cultured seeds. e germination frequency is higher in contaminated seeds than non-contaminated ones." (p. 4)

      "The bacteria available on the surface of contaminated seeds may act on degradation of the hard seed coat to remove the physical dormancy, thus triggering their germination." (p. 4)

      "f N. alba, with hardy seed coat by cutting it mechanically. tained from non-contaminated seeds may be due to the removal of dormancy through the scarification occurred in the seed preparation process." (p. 5)

      "Sulphuric acid was effective in establishing the contamination free cultures." (p. 5)

      "minated seedlings (χ = 125.03; p < 0.0001) (Figure 2a). omplete disinfection was observed in seeds treated with 50-100 % acid. The concentrations of 10 and 25 % acid, reduced the contamination rate over the control of untreated." (p. 5)

      "The greatest germination (6.3 %) was observed in the seeds treated with 75 % acid that gave 100 % disinfection." (p. 5)

      "nated and non-contaminated seedlings were observed. ctive in complete disinfection of the seeds, none of them germinated indicating the loss of seed viability in the concentrated acid." (p. 5)

      "aminated seedlings (χ = 10.89; p < 0.0279)t (Figure 2b). ation rate and the greatest frequency of the noncontaminated seedlings among the germinated were observed in the seeds treated for 60 and 180 seconds. Based on this observation, acid treatment for 60 seconds duration was selected as the optimum." (p. 5)

      "the occurrence of interaction (χ = 608.41; p < 0.0001). 5 %) was obtained by culturing the seeds treated with 75 % H2SO4 onto the solidified MS medium (Figure 3)." (p. 6)

      "The plants derived from the acid treated seeds showed a normal growth containing a well-grown shoot and the roots (Figure 4a, c) indicating that acid scarification had no adverse effect." (p. 6)

      "in the scarified seeds caused for better germination. medium supplemented with 0.5 mg/L 2, 4-D and 2.0 mg/L BAP, was effective in giving rise to well-grown complete seedlings, containing both shoots and roots with a higher germination rate (≈ 66 %)." (p. 6)

      "heavy contamination in the cultured seeds in vitro.e safe harbouring of bacteria during sterilisation process causing heavy bacterial contamination after culture initiation." (p. 6)

      "ations (10 % and 25 %) were not as effective as such. e Nymphaea species; N. alba (Sumlu et al., 2010; Latowski et al., 2014) and N. lotus var. thermalis (Blidar et al., 2019), which have no trichomes on the seed coats." (p. 6)

      "ermination of seeds by removing physicaln dormancy. ded the seed coat (Figure 4k) to the same degree of different acid treatments, allowing seed germination." (p. 7)

      "Although the study showed that seed culturing is a promising technique for in vitro propagation of N. nouchali, unawareness of the level of genetic purity of the seedling populations is a barrier for implementing the technique for conservation of true-to-type species." (p. 7)

      "enotypes into two major clusters (A and B; Figure 5b). elatedness within the plant populations." (p. 7)

      "The study revealed that a stable level of genetic uniformity existed within and among the three N. nouchali populations, suggesting the non-occurrence of gene contamination in these locations by undesirable alien alleles introduced by outcrossing." (p. 8)

      "undesirable alien alleles introduced by outcrossing. of these populations also suggests that the heterogeneity expected of the in vitro seedlings from these populations to be low, hence showing the possibility of using the technique for mass propagation from seeds collected from the isolated habitats." (p. 8)

    Attachments

    • Perera et al_2021_In Vitro culture of Nymphaea nouchali seeds; a conservation approach for a.pdf
    • Snapshot
  • Influence of ethanol and ethylene on the seed germination of three nymphaeid water plants

    Type Journal Article
    Author A.j.m. Smits
    Author G.h.w. Schmitz
    Author G. Van Der Velde
    Author L.a.c.j. Voesenek
    URL https://onlinelibrary.wiley.com/doi/abs/10.1111/j.1365-2427.1995.tb00421.x
    Volume 34
    Issue 1
    Pages 39-46
    Publication Freshwater Biology
    ISSN 1365-2427
    Date 1995
    Extra 00019 _eprint: https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1365-2427.1995.tb00421.x
    DOI 10.1111/j.1365-2427.1995.tb00421.x
    Accessed 11/17/2021, 8:06:31 PM
    Library Catalog Wiley Online Library
    Language en
    Abstract 1. Under anaerobic conditions cold stratified seeds of Nymphaea alba and Nuphar lutea germinated readily and released ethanol (up to 6–7 mM ethanol g-1 DW), whereas seeds of Nymphoides peltata did not germinate and hardly any ethanol was released (up to 1.5 mM ethanol g-1 DW). Ethylene release by seeds of Nymphaea, Nuphar and Nymphoides incubated under hypoxic conditions could not be detected. 2. Under aerobic conditions all Nymphaea and Nuphar seeds germinated, but at a lower rate compared with anaerobic incubation. Ethanol release under aerobic conditions was low (1.5–2 mM ethanol g-1 DW). Under aerobic conditions the seeds of Nymphoides germinated promptly and ethanol release was low (0–0.5 mM ethanol g-1 DW). 3. Germination of Nymphaea and Nuphar seeds in an ethanol solution (350 mM) was generally stimulated compared with that in water, but no significant effect was recorded if seeds had not received a cold treatment or had been stratified for 8 weeks. Germination of Nymphoides seeds was inhibited in the ethanol solution unless they had received a cold treatment of 12 weeks. 4. Germination of Nymphaea and Nuphar was stimulated by ethylene (5 νg 1-1) but germination in moist air was lower than under normal submersed conditions. A stimulating effect of ethylene on the germination of Nymphoides seeds was also evident. 5. It is suggested that ethanol and ethylene play an important role in determining niches for germination, contributing to the zonation of these nymphaeids in a water body.
    Date Added 11/17/2021, 8:06:31 PM
    Modified 1/23/2022, 9:07:24 PM

    Tags:

    • germination

    Notes:

    • Nymphaea and Nuphar seeds released more ethanol in the anaerobic incubation (up to 6-7 mM ethanol per g DW) than in the aerobic incubation (1-1.5 mM ethanol per g DW).

      No ethylene production by Nymphaea, Nuphar and Nymphoides seeds could be detected after 20 days of incubation.

      Ethylene stimulated the germination of Nymphaea, Nuphar and Nymphoides seeds. However, the total numbers of germinated seeds of Nymphar and in particular Nymphaea were low compared with those in the ethanol experiment.

       

    • Extracted Annotations (12/17/2021, 3:11:15 PM)

      "The seeds of Nymphaea and Nuphar germinated in both aerobic and anaerobic water. After 15 days of anaerobic incubation 60-70% of the seeds had germinated, as opposed to approximately 10-20% in the aerobic incubation (results not shown)." (p. 41)

      "Without a cold treatment only one or two Nymphaea, Nuphar and Nymphoides seeds germinated in the ethanol solution or in twice distilled water over a period of 60 days." (p. 42)

      "After a cold treatment of 4 weeks ethanol stimulated the germination of Nymphaea seeds" (p. 42)

      "Regardless of ethanol release, ethanol by itself (i.e. externally applied ethanol under aerobic conditions) appears to stimulate the germination of Nymphaea and Nuphar seeds." (p. 43)

      "The effect of externally applied ethanol (this study) does not match germination under anaerobic conditions (see also Smits et al, 1990b) and this is probably because externally added ethanol can only partly simulate the effect of endogenously produced ethanol." (p. 43)

      "It is suggested that ethanol production by Nymphaea and Nuphar seeds under anaerobic conditions and the germinationstimulating effect of ethanol together act as a selfaccelerating germination process." (p. 43)

      "Either no ethylene production occurred or the concentration of ethylene in the gas space of the incubation flasks was too low for detection." (p. 43)

      "It appears that the observed germination of Nymphaea and Nuphar seeds in moist air is retarded." (p. 44)

      "In this sense ethanol, as a characteristic compound of anaerobic metabolism that stimulates the germination of Nymphaea and Nuphar seeds, could be designated as a niche-specific compound for these species, indicating the presence of organic, anaerobic soils." (p. 44)

      "Anal ogous to this function of ethanol, ethylene could act as a niche-identifying compound for Nymphoides. The presence of ethylene can be expected in and just above sediments which are only periodically submersed and in which hypoxic conditions prevail, a prerequisite for ethylene production. This environment is most likely to be found in shallow water zones in combination with fluctuating water levels, the habitat where Nymphoides occurs frequently. The ethylene which is produced by micro-orgarusms in the sediment (or possibly released by the seeds themselves) stimulates the germination of Nymphoides." (p. 44)

      "The germination of Nymphaea and Nuphar is also stimulated by ethylene, but exposed conditions appear to hamper germination" (p. 44)

      "of these seeds, so that the overall effect is a low germination rate." (p. 45)

      "In contrast to Nymphoides the seedlings of Nymphaea and Nuphar desiccate readily after emergence." (p. 45)

      "It was suggested above that ethanol and ethylene affect germination in such a way that they could act as niche-identifying substances. However, their action is just part of a chain of events which eventually lead to stimulation or postponement of germination." (p. 45)

      "Anaerobic conditions, the presence of ethanol and darkness are associated with the deeper parts of a water body. The germination of Nymphaea and Nuphar seeds is stimulated by anaerobic conditions and ethanol." (p. 45)

      "In the littoral zone, aerobic or hypoxic conditions prevail in the sediment, which contains less organic material and is subjected to fluctuating water levels. Under aerobic conditions, low germination rates of Nymphaea and Nuphar seeds have been recorded, while the germination rate of Nymphoides seeds is high. Moreover, in contrast to Nymphoides seeds the germination of Nymphaea and Nuphar seeds under conditions where ethylene can be produced is low." (p. 45)

      "The seeds of all three plant species are able to germinate under dark conditions. The germination of seeds of all species, in particular Nymphoides, is stimulated by light." (p. 45)

      "From these data it can be deduced that the germination of Nymphaea and Nuphar is stimulated by factors associated with soft, organic sediments, in which dark and anaerobic conditions prevail." (p. 45)

    Attachments

    • Smits et al_1995_Influence of ethanol and ethylene on the seed germination of three nymphaeid.pdf
    • Snapshot
  • MADS-box genes expressed during flower development and fruit maturation in Nymphaea caerulea

    Type Journal Article
    Author Silvia Moschin
    URL https://www.research.unipd.it/handle/11577/3426234
    Publication undefined
    Date 2018
    Extra 00000
    Accessed 1/18/2022, 11:52:01 PM
    Library Catalog www.semanticscholar.org
    Language en
    Abstract A complex scenario for the expressed MADS-box genes in floral developing tissues was obtained, which reflects the complex floral morphology of the water lily and is in accordance with previous studies conducted in basal Angiosperms’ flowers. MADS-box genes have been found in all eukaryotes, but their number has greatly expanded in plants, where their functions range from root development to floral organ specification and to fruit development. During the development of flowers, some of them act as homeotic selector genes specifying the identity of the floral organs, according to the ABC(D)E model. The model was developed thanks to many studies carried out in eudicots and it works quite well to explain their flower development. By contrast, for many basal Angiosperms the same model does not fit equally well, because their flowers may be organized with a different architecture and their floral organs are not always similarly well defined. For instance, they may show transition forms for some of the floral components. My PhD project studied MADS-box genes expressed in the developing reproductive structures of the basal Angiosperm Nymphaea caerulea. The work has started with gene isolation, since no MADS-box sequence belonging to this species could be found in public databases. To isolate as many as possible MADS-box genes several starting samples and methods have been used. Overall, I was able to isolate the following different MADS-box genes from both flower and fruit tissues: APETALA1/FRUITFULL, APETALA3 (three splicing variants and two resulting proteins of different length), PISTILLATA, three different AGAMOUS-like genes (i.e. AG1, AG2, and AG3), SEPALLATA, AGL6, and JOINTLESS. Thus, genes belonging to all the functional classes of the canonical ABC(D)E model of flower development have been obtained and identified. A detailed expression analysis of the isolated genes during flower and fruit development has revealed some interesting results. A complex scenario for the expressed MADS-box genes in floral developing tissues was obtained, which reflects the complex floral morphology of the water lily and is in accordance with previous studies conducted in basal Angiosperms’ flowers. Considering that some MADS-box transcription factors involved in flower development are important also to regulate post-fertilization processes, I also studied in detail the N. caerulea fruit development, which appeared an interesting and finely tuned process. The study of fruit maturation in a water lily represents the most novel aspect of this work. N. caerulea has a pluricarpellate ovary that after fertilization develops into a fleshy capsule. It matures underwater until its opening occurs to disperse a multitude of arillate seeds. Detailed observations of the fruit opening evidenced some specific zones involved in cell separation events like those that occur in the abscission zones of petioles and pedicels in terrestrial organs. Such interesting observations have been supported by the expression of genes involved in the determination (i.e. JNT) and in the activation (i.e. AG2) of these zones, but also by the presence of some cell wall degrading/modelling enzymes that may cause the separation events which trigger the fruit opening. Finally, I noticed also that the actual seeds dispersion in this species is not carried out directly by its fleshy capsule, which almost completely dissolves in water shortly after its opening, rather by the soft arils that surround the seeds.
    Date Added 1/18/2022, 11:52:01 PM
    Modified 5/13/2022, 5:28:34 PM

    Tags:

    • genetic

    Notes:

    • Annotations
      (5/13/2022, 5:44:23 PM)

      “Proceeding from the exterior towards the centre of the flower we find: the four outermost tepals that enclose the bud and have a greenish abaxial surface and a whitish adaxial one (Figure 3.2 A: “1”). All the other tepals have both surfaces with a cerulean appearance and look therefore like vexillary elements proper (Figure 3.2 A: “2” and “3”). They exhibit a gradual centripetal reduction in size to the point of stamens attachment, thus they have been further separated in outer and inner ones (“2” and “3” respectively).” (Moschin, 2018, p. 17)

      “While the outermost tepals (with a sepal-like aspect) are always four, the same cannot be said for the other tepals: observations made on twenty-four flowers showed a variability between twelve and twenty units, while the most frequent values are between sixteen and nineteen units.” (Moschin, 2018, p. 17)

      “Similarly to tepals, also stamens are spirally arranged, showing a gradual transition from: the outer lager stamens characterized by a cerulean tip (the more distal portion of the element, marked with “4” in Figure 3.2 B), to the innermost stamens (“6”), smaller and without any distal cerulean portion. Thanks to the partial ornamental appearance, the outermost stamens can be further named “petaloid stamens”.” (Moschin, 2018, p. 17)

      “At the centre of the flower a syncarpous pluricarpellary gynoecium can be observed. It is arranged radially around a central core of receptacular tissue (Moseley, 1961). (Figure 3.2 B: “8”). The semiinferous syncarpic ovary clearly shows a number of fused carpels (Figure 3.2 B: “7”) equal to the number of petals.” (Moschin, 2018, p. 17)

      “Observing more in detail the petaloid stamens, it has been possible to see that below the cerulean tip there is an anther with four pollen sacs (Figure 3.3 A), which is comparable to the anther of the innermost stamens (Figure 3.3 B).” (Moschin, 2018, p. 19)

      “After fertilization, the flower closes for the last time and thanks to a curvature of the peduncle it sinks into the muddy ground where it matures for about three weeks.” (Moschin, 2018, p. 19)

      “The pluricarpellate ovary is transformed into a fleshy capsule that develops underwater for about 23-25 days from anthesis (the duration of the process depends also on climatic conditions).” (Moschin, 2018, p. 19)

      “The seeds of N. caerulea are almost completely enclosed by an aril that develops from the funiculus, in an area at the bottom of the developing seeds.” (Moschin, 2018, p. 19)

      “Based on the analysis of 25 different fruits, it has been noted that seeds and arils follow a quite constant maturation pattern, independently from the size of the capsule. In the very first stage of development (i.e. at 4-5 days post anthesis, thus immediately after fertilization) seeds are tiny, soft and orange (Figure 3.4 A). At about 10 days post anthesis (10 DPA) they rapidly increase their size and exhibit a bright red colour. At this stage also the arils start to develop (Figure 3.4 C), from the bottom of the seeds. Then, the growing seeds change colour becoming bordeaux, and the partial arils start to envelop them (Figure 3.4 D). Once the arils have completed their growth enveloping almost completely the seeds, the latter appear more or less brownish (Figure 3.4 E/F).” (Moschin, 2018, p. 20)

      “The aril represents a common character of the family Nymphaeaceae (with the exception of the genera Barclaya and Nuphar) (Bonilla-Barbosa et al., 2000). It consists of a translucent fleshy and tiny envelope that extends its growth from the funiculus enclosing almost completely the mature seed (Figure 3.5). This interesting structure has a great evolutionary importance: with its particular shape, it traps air around the seeds, allowing them to float once the fruit opens (Figure 3.6). Through that, seeds have some time to be transported away by water movements (hydrochory), thus to be dispersed.” (Moschin, 2018, p. 20)

      “Moreover, arils are mucilaginous and also rich in starch (Figure 3.7), therefore the floatin” (Moschin, 2018, p. 20)

      “14 arillate seeds may be eaten by birds and dispersed through endozoochory. Hence it clearly appears that it is the aril the structure actually involved in the dispersal of seeds.” (Moschin, 2018, p. 21)

      “Nymphaea caerulea has a pluricarpellate ovary that develops underwater into a fleshy capsule after the flower is fertilized. The fruit is dehiscent, when it reaches full maturity it opens at the water surface releasing the mature seeds which are almost completely enveloped by a thin translucent aril that allows them to float (chapter 3). Both the maturation process and the fruit opening are finely regulated.” (Moschin, 2018, p. 90)

      “The microscopical analyses led us to hypothesize that the fruit opening occurs thanks to specific and finely localized cell separation events like those that occur in the abscission zones of petioles and pedicels at the level of aerial organs of terrestrial plants.” (Moschin, 2018, p. 90)

      “Observing several maturing fruits, it has been possible to understand that the entire developing process until the fruit opening lasts about 23-25 days from the anthesis. Thus, different fruits that were about to open have been collected, transported to the laboratory and put inside a little basin full of water so that their opening could be filmed and photographed.” (Moschin, 2018, p. 90)

      “These morphological observations suggest that the fruit opening occurs through a series of cell separation events comparable to those that occur during the processes of organ abscission in terrestrial plants. These internal detachments, together with the pressure made by the seed arils, cause a rapid structural failure of the pericarp walls.” (Moschin, 2018, p. 93)

      “My doctorate work revealed the presence of cell wall degrading enzymes in the zones that undergo to a more or less massive process of cell separation during fruit maturation (Figure 7.5). Such zones correspond to the points where the various carpels join, at the level of the top portion of the fruit, or where carpels are anchored to the fruit backbone, at the level of the central core and at the level of the bottom portion (Figure 7.4).” (Moschin, 2018, p. 100)

    Attachments

    • Moschin_2018_MADS-box genes expressed during flower development and fruit maturation in.pdf
    • Snapshot
  • Multivariate analysis of Nymphaea (Nymphaeaceae) taxa in Manipur (India) through morphological variables

    Type Journal Article
    Author Sagolsem Asharani Devi
    Author Biseshwori Thongam
    Author Pratap Jyoti Handique
    URL https://doi.org/10.1007/s40415-015-0231-1
    Volume 39
    Issue 1
    Pages 359-366
    Publication Brazilian Journal of Botany
    ISSN 1806-9959
    Date 2016-03-01
    Extra 00000
    Journal Abbr Braz. J. Bot
    DOI 10.1007/s40415-015-0231-1
    Accessed 11/17/2021, 5:22:42 PM
    Library Catalog Springer Link
    Language en
    Abstract Nymphaea L. forms an economically important wetland plant of Manipur, India. However, there is a dearth of the diversity information about the Nymphaea in this region. There is availability of great variation in the Nymphaea taxa collected during the survey. A total of 40 morphological characters were evaluated and analysed in 207 individuals representing nine taxa, through principal component analysis. The results indicate that there are three distinct types of morphologically same construct Nymphaea taxa detected as components. The first component consists of five taxa, viz., N. micrantha, N. caerulea, N. nouchali, N. manipurensis and N. manipurensis var. versicolor, which can explain around 33 % of the total variation of the Nymphaea taxa. Two taxa, including N. × marliacea and N. mexicana, form the second component that contributes around 30 % of the total variation of the Nymphaea taxa. The last component pertains to N. rubra and N. pubescens that can explain the variation of the Nymphaea taxa by 12 % approximately. Finally, the three components so far identified are designated as a triangular rhizome group, tubular rhizome group and globular rhizome group, respectively. The present study emphasizes the importance of morphological characters in delimiting the taxonomic groups in the Nymphaea taxa.
    Date Added 11/17/2021, 5:22:42 PM
    Modified 11/17/2021, 5:22:43 PM

    Notes:

    • Annotations
      (5/28/2022, 3:54:58 PM)

      “Nymphaea flowers show a variety of colours, and few genera of plants offer such variety in size and colour of flowers, as is found among the water lilies (Conard 1905).” (Devi et al., 2016, p. 360)

      “A survey was carried out during 2010–2012, in the home ponds, paddy fields and wetland habitats in the Manipur state of North East India (Fig. 1).” (Devi et al., 2016, p. 360)

      “Altogether nine Nymphaea taxa were collected: seven known taxa, namely Nymphaea micrantha Guill. and Perr., N. nouchali Burm.f.,N. rubra Roxb. ex Andrews, N. mexicana Zucc., N. 9 marliacea Hort ex Lat.-Marl., N. pubescens Willd. and N. caerulea Savigny, and two unidentified taxa, namely N. manipurensis Asharani & Biseshwori and N. manipurensis var. versicolor Asharani and Biseshwori, during the sample surveys.” (Devi et al., 2016, p. 360)

      “High range and variety of the vegetative characters and the availability of many hybrids have been the major challenges in specific delimitation.” (Devi et al., 2016, p. 364)

      “Members of subgenus Brachyceras have triangularshaped rhizomes; globular rhizomes are observed in subgenus Lotos, whereas cylindrical rhizomes are observed in subgenus Nymphaea.” (Devi et al., 2016, p. 364)

    Attachments

    • Devi et al_2016_Multivariate analysis of Nymphaea (Nymphaeaceae) taxa in Manipur (India).pdf

      Contents

      • Abstract
      • Introduction
      • Materials and methods
        • Plant material
        • Characterization and evaluation
        • Statistical analysis
      • Results
      • Discussion
      • Acknowledgments
      • References
  • Nymphaea nouchali var. versicolor ‘Bua Phuean’: Seed Morphology and Germination In Vitro

    Type Journal Article
    Author Kitti Bodhipadma
    Author Sompoch Noichinda
    Author Phetcharat Wachirabongkoth
    Author Ekawut Pukpoomin
    Author Luepol Punnakanta
    Author Koravisd Nathalang
    URL https://ph02.tci-thaijo.org/index.php/ennrj/article/view/82475
    Rights Copyright (c) 2017 Environment and Natural Resources Journal
    Volume 9
    Issue 2
    Pages 19-25
    Publication Environment and Natural Resources Journal
    ISSN 2408-2384
    Date 2011
    Extra 00001 Number: 2
    Accessed 11/17/2021, 2:18:19 PM
    Library Catalog ph02.tci-thaijo.org
    Language en
    Abstract Nymphaea nouchali var. versicolor ‘Bua Phuean’ is one of Thai native species of day-blooming waterlily. Since the expansion of community from metropolitan area and the appreciation on exotic species of Nymphaea, number of this plant in environment is noticeably decreased. One of the efficient methods to conserve and increase the amount of this plant is seed germination. Thus, seed morphology and developmental stages of ‘Bua Phuean’ were investigated before germinating in vitro. The results revealed that ‘Bua Phuean’ seeds could be categorized into 5 stages and each stage also had dissimilar morphology. After the stages 3 to 5 seeds were germinated under aseptic condition, seed in stage 5 showed the highest germination rate at 82.22 %. During seed germination, coleoptile emerged from seed coat before root became visible.
    Short Title Nymphaea nouchali var. versicolor ‘Bua Phuean’
    Date Added 11/17/2021, 2:18:19 PM
    Modified 1/23/2022, 9:07:24 PM

    Tags:

    • in vitro
    • germination
    • aseptic condition
    • germination rate
    • Nymphaea nouchali
    • seed stage
    • seedling development

    Notes:

    • Extracted Annotations (11/17/2021, 6:49:23 PM)

      "Seeds of each selected stage were separately rinsed with clean running tap water for 10 min and washed in distilled water. Seeds were immersed for 15 min in 5% (v/v) Clorox (a commercial bleach solution containing 5.25%, w/w, sodium hypochlorite as available chlorine) to which 2 drops of Tween-20 were added. The samples were rinsed 3 times with sterile distilled water each for 5 min before placing on Murashige and Skoog (MS) basal medium (Murashige and Skoog, 1962)." (p. 20)

      "Afterward, 15 ml of sterile distilled water was poured over the seeds on semi-solid medium." (p. 20)

      "Cultures were then kept in a growth room under dark condition or 16 hr of illumination from cool white fluorescent lamps (44.57 μmol/m2/s light intensity) and 8 hr of darkness at 25±2 °C." (p. 20)

      "With the naked eye, the different color of seeds could be seen in dissimilar stages of fruits. According to the diverse seed colors, 'Bua Phuean' fruits were classified into stage 1 to 5 which contained orange-red, red, light brown, brown and dark brown seeds, respectively (Figure 2)." (p. 20)

      "stage 5: seed coat was dark brown, rows of longitudinal trichomes present and thick air-containing sack-like, pulpy aril covered." (p. 20)

      "At some point in seed surface sterilization, spongy aril was mangled. Thus, all surface-sterilized seeds that placing on the MS basal medium was uncovered with the aril." (p. 22)

      "highest germination percentage was obtained from stage 5 seeds at 82.22 (Figure 5). These findings illustrated that mature seeds of 'Bua Phuean' had higher germinability than the younger ones." (p. 22)

      "Moreover, the results also suggested that light promoted germination in 'Bua Phuean' seeds as none of seeds from stage 3 to 5 were found germinating under dark condition (Figures 5 and 6)." (p. 22)

      "The coleoptile (plumular sheath) protruded out of seed coat before the first foliage leaf emerged (Figure 7). Afterward, root became noticeable and the first foliage leaf began expanding." (p. 23)

      "Seed germination of 'Bua Phuean' in our experiment did not require cold stratification or perform any dormancy like in some reports (Estrelles et al., 2004; Sumlu et al., 2010)." (p. 24)

      "In the present study, seeds from stage 4 and 5 apparently had the potential for plant propagation even though the highest survival rate was from stage 5." (p. 24)

    Attachments

    • Bodhipadma et al_2011_Nymphaea nouchali var.pdf
  • Pharmocognostic studies on Nymphaea spp.

    Type Journal Article
    Author Archana Pareek
    Author Ashwani Kumar
    Volume 5
    Issue 6
    Pages 18
    Publication World Journal of Pharmaceutical Research
    ISSN 2277-7105
    Date 2016
    Extra 00000
    DOI 10.20959/wjpr20166-6285
    Library Catalog Zotero
    Language en
    Abstract Wetlands provide a unique habitat for several medicinal plants attempt has been made to document some of the little known medicinal properties of wetland plants used by local community of India. Nymphaea is a genus of aquatic perennial plants having showy flowers (white, blue, pink, or yellow, often fragrant), including the white water lily currently Nymphaea, they are growing from an under water stem. which is buried in the mud and sends root lets for anchorage. Water lily, the member of the Nymphaeaceae family, is the symbol of Buddhism and Brahmanism in India. The plant has great medicinal value. Present review deals with various species and their applications in traditional medicines.
    Date Added 11/17/2021, 8:10:18 PM
    Modified 11/17/2021, 9:43:38 PM

    Notes:

    • Extracted Annotations (12/24/2021, 4:34:58 PM)

      "The sample of selected plants were collected from different parts of Rajasthan from water bodies and marshy areas." (p. 19)

      "A large, aquatic herb with tuberous rhizome and peltate leaves, flowers solitary, fragrant, variable in colour, deep red to pure white, fruit a spongy berry." (p. 23)

      "Part of the leaves is submerged, while others rise slightly above the surface. The leaves are round and green on top; they usually have a darker underside. The floating leaves have undulating edges that give them a crenellate appearance. Their size is about 20-24 cm and their spread is 0.8 to 1.9 m." (p. 23)

      "Nymphaea nouchali is a day-blooming nonviviparous plant with submerged roots and stems." (p. 23)

    Attachments

    • Pareek_Kumar_PHARMOCOGNOSTIC STUDIES ON NYMPHAEA SPP.pdf
  • Photosynthesis in the Blue Water Lily (Nymphaea caerulea Saligny) Using Pulse Amplitude Modulation Fluorometry

    Type Journal Article
    Author Raymond J. Ritchie
    URL https://www.journals.uchicago.edu/doi/abs/10.1086/663168
    Volume 173
    Issue 2
    Pages 124-136
    Publication International Journal of Plant Sciences
    ISSN 1058-5893
    Date February 1, 2012
    Extra 00025 Publisher: The University of Chicago Press
    DOI 10.1086/663168
    Accessed 11/17/2021, 2:46:59 PM
    Library Catalog journals.uchicago.edu (Atypon)
    Abstract Water lilies, such as the blue Egyptian water lily (Nymphaea caerulea Savigny), are ubiquitous aquatic plants. Leaves of mature plants normally unfold at the surface and are floating or emergent. Some aquatic vascular plants have a form of CAM (crassulacean acid metabolism) known as submerged aquatic metabolism (SAM). The presence of aerenchyma in water lily leaves and petioles makes it very difficult to measure photosynthesis in water lily plants by gas exchange. Pulse amplitude modulation (PAM) fluorometer techniques provide direct information on the light reactions of plants. PAM technology calculates photosynthesis as the electron transport rate (ETR) through PSII (4 electrons per O2 produced) in mol m−2 s−1. Here, relative ETR (rETR) was based on an assumed leaf absorptance factor of 0.84. Photosynthesis-versus-irradiance (P vs. E) curves were fitted with the waiting-in-line function (). Maximum effective quantum yield, maximum relative ETR (rETRmax), and quantum efficiency all vary on a diurnal cycle. The nonphotochemical quenching parameters qNmax and NPQmax are highly correlated with each other (, ) but do not show a systematic variation over a diurnal cycle. Nymphaea is a “sun plant” with optimum irradiance (Eopt) of 1000 μmol m−2 s−1 PPFD or higher. Titratable acid of leaves varied from ∼50 to 70 mol H+ m−3 (leaf water basis) and was depleted at ∼0600 and 1800 hours each day, a diel pattern inconsistent with SAM/CAM physiology. The N. caerulea C4 acid pool is too small to support substantial SAM-type metabolism. Gross photosynthesis of Nymphaea leaves had a high value of ∼5.3 g C m−2 d−1. For a daily irradiance of 56 mol m−2 PPFD, this works out to a 3.3% conversion efficiency in terms of moles of carbon.
    Date Added 11/17/2021, 2:46:59 PM
    Modified 11/17/2021, 2:47:01 PM

    Tags:

    • CAM photosynthesis
    • carbon fixation
    • diurnal cycle
    • gross photosynthesis
    • light curves
    • PPFD
    • primary productivity
    • pulse amplitude modulation fluorometry
    • submerged aquatic metabolism

    Notes:

    • Extracted Annotations (11/17/2021, 6:29:59 PM)

      "Blue Egyptian water lilies (Nymphaea caerulea, Savigny) are grown as decorative plants in circular earthenware bowls (30 L) on the Phuket campus of Prince Songkla University, Phuket Province, Thailand (lat. 7°539N, long. 98°249E) in June 2011." (p. 127)

      "They are not fertilized, and they rely on rainwater most of the year and tap water in the dry season." (p. 127)

      "Maximum effective photosynthetic yield (Ymax) by Nymphaea was only;0.2-0.3 for leaves sampled during the night, rose to;0.5-0.6 at midday, but then steadily declined back to nighttime levels by sunset (fig. 1)." (p. 128)

      "The rETRmax was 55:36 1:24mmol m2 s1, and the optimum irradiance (Eopt) was 9206 39:1mmol m2 s1 PPFD, or;44% of full sunlight at the season when the study was done in Phuket (fig. 1)." (p. 128)

      "The photosynthetic efficiency (a) was 0:16346 0:00785, which is somewhat lower than a typical value found for C3 vascular plants (Ritchie 2008) or CAM plants (Ritchie and Bunthawin 2010a, 2010b)." (p. 128)

      "The approximate maximum Pg rate would be 13:86 0:31mmol O2 m2 s1." (p. 128)

      "For leaves collected during the day, the Eopt value was ;900mmol m2 s1 PPFD, but Eopt values were lower early in the morning and at night." (p. 129)

      "The Pg of a layered battery of Nymphaea leaves would not saturate during the middle of the day and would reach a maximum theoretical carbon fixation rate of 700mg C m2 s1 (;7 times that achieved by the Nymphaea leaves; fig. 7), or ;16.4 g C m2 d1 (fig. 8)." (p. 132)

      "The pattern of titratable acid in the leaves of Nymphaea, however, is not consistent with any significant CAM physiology (fig. 6; cf. Ritchie and Bunthawin 2010a, 2010b)." (p. 133)

      "This study shows that the amount of organic acid stored in Nymphaea leaves is so small, compared to that in classical CAM plants (300 to>1000mmol Hþ g1 FW; Luttge 2007) and SAM/CAM plants (Isoetes300mmol Hþ g1 FW; Keeley 1983), that it would provide only;15 min supply of CO2 at midday rates of photosynthesis." (p. 133)

      "Figures 2 and 3 show that Nymphaea is a sun plant able to maintain very high rates of photosynthesis in full sunlight (2110mmol m2 s1 PAR). During daylight, the optimum irradiance (Eopt) is of the order of 1000mmol m2 s1 PAR (table 2), similar to that found by Snir et al. (2006), using PAM methods, in Nuphar lutea." (p. 133)

      "C4 photosynthesis in nymphaeids is improbable. The C4 acid pool in Nymphaea leaves is unlikely to act as a carbon storage step in a C4 carbon-concentrating mechanism." (p. 133)

      "The high optimum irradiance (Eopt) of;1000mmol m2 s1 PPFD (table 2; fig. 3) clearly places Nymphaea on the high end of what rates as a sun plant: most plants with such high optimum irradiances are C4 (Atwell et al. 1999)." (p. 134)

      "The Pg achievable by Nymphaea (5.3 g C m2 d1; figs. 7, 8) is comparable to that of a well-kept field crop or pasture of a C3 plant (Atwell et al. 1999)." (p. 134)

      "The finding in this study that Nymphaea leaves have a potential Pg of 5.3 g C m2 d1 is very impressive when it is noted that it is achieved by a single leaf acting as a horizontal photosynthetic surface having a palisade mesophyll with only 2 or 3 cells" (p. 134)

      "Since irradiance reached more than 2100mmol m2 s1 at midday in Phuket during the time of the study, equation (3) predicts substantial photoinhibition of photosynthesis during the middle of the day, but the inhibition was less than 50% because of the very high optimum irradiance." (p. 134)

      "stacked on top of each other (Kaul 1976; Hough and Wetzel 1977)." (p. 135)

      "In terms of converting a total daily irradiance of 57 mol m2 PPFD into moles of carbon, the photosynthetic efficiency is 3.3%." (p. 135)

      "The daily cumulative Pg shown in figure 8 shows that a water lily pond completely covered by leaves is capable of about one-third of the theoretical maximum carbon fixation rate, even under nutrient-limited conditions." (p. 135)

    Attachments

    • Ritchie_2012_Photosynthesis in the Blue Water Lily (Nymphaea caerulea Saligny) Using Pulse.pdf
  • Reproductive Biology of Nymphaea (Nymphaeaceae)

    Type Journal Article
    Author John H. Wiersema
    URL https://www.jstor.org/stable/2399367
    Volume 75
    Issue 3
    Pages 795-804
    Publication Annals of the Missouri Botanical Garden
    ISSN 0026-6493
    Date 1988
    Extra 00070 Publisher: Missouri Botanical Garden Press
    DOI 10.2307/2399367
    Accessed 11/17/2021, 8:02:59 PM
    Library Catalog JSTOR
    Abstract Several reproductive strategies have evolved within the genus Nymphaea. Sexual reproduction is mostly protogynous; flowers are open two to several days (depending on the species), with pollen release usually commencing on the second day. The five subgenera of Nymphaea exhibit differences in floral biology. There is considerable variation in the timing of flower opening, floral odor, flower color, and the form and function of various flower parts. These differences may contribute to genetic isolation between species both through temporal separation of flowering and attraction of different pollinators. While sexual reproduction in many species is dependent on xenogamy or geitonogamy, other species have adaptations to promote autogamy. No species of Nymphaea is known to be agamospermous, but several other modes of asexual reproduction are exhibited: detachable tubers, stolon formation, and proliferations of floral and foliar tissue. Wide-ranging tropical species all avoid being totally reliant on pollinators by employing one or more reproductive alternatives to outcrossing; clearly some obligate outcrossers are limited in their colonizing by pollinator availability. The most important of these reproductive alternatives is autogamy. Wide-ranging temperate species, which mostly rely exclusively on outcrossing for sexual reproduction, probably avoid pollinator limitations by utilizing a broader range of pollinators.
    Date Added 11/17/2021, 8:02:59 PM
    Modified 11/17/2021, 8:02:59 PM

    Notes:

    • Annotations
      (4/25/2022, 3:18:14 PM)

      “Autogamy has also been reported among other members of subg. Brachyceras, such as N. caerulea and N. stellata Willd. (Conard, 1905)” (Wiersema, 1988, p. 800)

    Attachments

    • Wiersema_1988_Reproductive Biology of Nymphaea (Nymphaeaceae).pdf

      Contents

        • p. [795]
        • p. 796
        • p. 797
        • p. 798
        • p. 799
        • p. 800
        • p. 801
        • p. 802
        • p. 803
        • p. 804
  • Role of Brycinus lateralis (Teleostei: Alestidae) in dispersal and germination of Nymphaea nouchali (Angiospermae: Nymphaeaceae) seeds on a seasonal floodplain of the Okavango Delta, Botswana

    Type Journal Article
    Author M Mmusi
    Author K Mosepele
    Author M Murray-Hudson
    Author D Teketay
    Author M Horn
    URL https://doi.org/10.2989/16085914.2016.1244041
    Volume 41
    Issue 4
    Pages 489-494
    Publication African Journal of Aquatic Science
    ISSN 1608-5914
    Date December 15, 2016
    Extra 00001 Publisher: Taylor & Francis _eprint: https://doi.org/10.2989/16085914.2016.1244041
    DOI 10.2989/16085914.2016.1244041
    Accessed 12/4/2021, 8:36:05 PM
    Library Catalog Taylor and Francis+NEJM
    Abstract Seed passage through the gut of vertebrates can be important for seed dispersal, but might influence seed viability. The ability of seeds to germinate after ingestion by seed-eating fish is important for the population dynamics of some plant species, and significant in the evolution of plant–fish interactions. Certain fish in the Okavango Delta, Botswana, are fruit- and seed-eaters and could act as seed dispersers. We sampled 14 fish species in 2013, finding Nymphaea nouchali var. caerulea seeds in the digestive tracts of eight, most commonly in the striped robber Brycinus lateralis. Seeds extracted from the gut of this species had an overall mean germination success of 11.7%. This fish species might well be a legitimate seed disperser, having a positive effect on seed dispersal from parent plants in the Okavango Delta. The current study represents one of the first investigations of the likelihood of seed dispersal by fish on the African continent.
    Short Title Role of Brycinus lateralis (Teleostei
    Date Added 12/4/2021, 8:36:05 PM
    Modified 1/23/2022, 9:07:24 PM

    Tags:

    • germination
    • seed germination
    • digestive tract
    • frugivore
    • seed ingestion
    • seed passage

    Notes:

    • Annotations
      (4/6/2022, 6:18:26 PM)

      “Seeds extracted from the gut of this species had an overall mean germination success of 11.7%.” (Mmusi et al., 2016, p. 1)

      “The seeds were placed in Petri dishes lined with cotton wool, which was saturated with distilled water twice per day. The water and cotton wool were changed every three days to avoid fungal or algal growth, which could affect germination.” (Mmusi et al., 2016, p. 3)

      “Of the fourteen species of fish collected in the Thamalakane and Boro rivers, eight contained seeds in their digestive tracts. All seeds belonged to the aquatic flowering plant Nymphaea nouchali (Table 1).” (Mmusi et al., 2016, p. 3)

      “Most seeds of N. nouchali retrieved from B. lateralis guts did not germinate, but those seeds might have been viable, yet dormant, and therefore available to germinate during the next favourable season.” (Mmusi et al., 2016, p. 4)

      “The plants available in the surroundings of the nets were not limited to N. nouchali, because the B. lateralis sampled were found to have consumed several other items of aquatic and terrestrial origin.” (Mmusi et al., 2016, p. 4)

    Attachments

    • Mmusi et al_2016_Role of Brycinus lateralis (Teleostei.pdf
    • Snapshot
  • Screening of Phytochemical Constituents of Nymphaea Caerulea savigny. An Aquatic Plant Resource for Drug Development

    Type Journal Article
    Author K Siva Prasad
    Author N Savithramma
    Volume 4
    Issue 4
    Pages 45-54
    Publication American Journal of Advanced Drug Delivery
    ISSN 2321-547X
    Date 2016
    Extra 00002
    Library Catalog Zotero
    Language en
    Abstract Objectives: Nymphaea caerulea Savigny. is multipurpose medicinal plant has been mentioned for the treatment of liver disorders in Ayurveda, an ancient system of medicine. Hence the Phytochemical evaluation and estimation of secondary metabolites were carried out. Methods: Polar and non-polar solvents were used to extract maximum number of compounds from various plant parts of N. caerulea preliminary screening analysis (Gibbs, 1974) and quantitative estimation of phytochemicals (Makkar et al., 1993) was carried out. Results: The results revealed that the plant is a rich source of different secondary metabolites like anthocyanins, anthraqunones, emodins, fatty acids, flavonoids, luecoanthocyanins, glycosides, phenols, coumarins, tannins and triterpenoids. Methanol, ethanol, chloroform and water extracts of leaf and flower are excellent source of phytocostituenpts when compare with rhizome and root. Conclusion: The findings of the study will be helpful to the pharmacologists and phytochemists for identification of novel potential active compounds.
    Date Added 12/18/2021, 3:46:34 PM
    Modified 4/6/2022, 5:57:12 PM

    Tags:

    • phytochemistry

    Notes:

    • Annotations
      (4/6/2022, 6:10:59 PM)

      “Roots, rhizomes, leaves and flowers (Fig.2 b, c, e and f) were collected from palakonda hills near palakondaraya temple, kadapa District.” (Prasad and Savithramma, 2016, p. 2)

      “The phytochemical screening of various parts of N. caerulea showed that they are rich in phenols, flavonoids, saponins, anthraquinones and anthocyanins present in all plant parts but leaves and flowers are showing all phytochemicals in methanol, ethanol and chloroform extractions.” (Prasad and Savithramma, 2016, p. 3)

      “Leaves and flowers have more number of secondary metabolites than the rhizome and roots (Table-1). Triterpenoides, alkaloids are absent in root whereas leucoanthocyanins, anthraquinones, triterpenoides and alkaloids are absent in rhizome.” (Prasad and Savithramma, 2016, p. 3)

      “Alkaloids are found only in aqueous extract of flower and leaf.” (Prasad and Savithramma, 2016, p. 3)

      “The highest total flavonoid content was found in flowers (0.02275 mg QE/g (Quercetin Equivalent)/g) followed by leaf (0.012 QE/g) whereas absent in rhizome and root.” (Prasad and Savithramma, 2016, p. 5)

      “The highest total phenols content was found in leaf (325 mg TAE (Tannic Acid Equivalent)/g) than flower (315 mg TAE/g), rhizome (210 mg TAE/g) and root (1801 mg TAE/g) (Table-2).” (Prasad and Savithramma, 2016, p. 5)

      “The highest total tannins cotent was found in the leaf (90.156 mg TAE/g) and followed by flower (0.11225 mg TAE/g).” (Prasad and Savithramma, 2016, p. 5)

    Attachments

    • Prasad_Savithramma_Screening of Phytochemical Constituents of Nymphaea Caerulea savigny.pdf
  • Selective insectivory in Nymphaea nouchali Burm. f.

    Type Journal Article
    Author Pundarikakshudu Tetali
    Author Shrikant Sutar
    Author Sujata Tetali
    URL https://www.nature.com/articles/npre.2008.1817.1
    Rights 2008 The Author(s)
    Pages 1-1
    Publication Nature Precedings
    ISSN 1756-0357
    Date 2008-04-21
    Extra Bandiera_abtest: a Cg_type: Nature Research Journals Primary_atype: Research Publisher: Nature Publishing Group
    Journal Abbr Nat Prec
    DOI 10.1038/npre.2008.1817.1
    Accessed 12/24/2021, 5:42:12 PM
    Library Catalog www.nature.com
    Language en
    Abstract Carnivorous plants comprise roughly 0.24 percent of the flowering plants, or 640 species represented in 12 families. Yet they are regarded as miracula naturae. Over fifty percent of these taxa are represented in a single family, namely Lentibulariaceae. Carnivorous plants are generally insectivorous, and carnivory in flowering plants is generally found in taxa that are adapted to nutrient-deficient habitats. The extra nutrients such plants acquire by special ways serve merely as supplements. The origin and evolution of carnivorous plants is a mystery in the phylogenetic tree of angiosperms, they often appear without a clear linkage. Here, we report that Nymphaea nouchali Burm. f. (a cultivar of var. cernua), a large aquatic member of the family Nymphaeaceae, indulges in a primitive form of insectivory and represents the missing evolutionary link. To the best of our knowledge, an insectivorous flower was not reported in flowering plants before.
    Date Added 12/24/2021, 5:42:12 PM
    Modified 1/23/2022, 9:26:26 PM

    Tags:

    • morphology
    • flower
    • insectivory

    Notes:

    • Extracted Annotations (1/23/2022, 9:25:45 PM)

      "As soon as an insect lands on the stamen, the filament bends inwards to make the insect fall into the stigmatic cup filled with the watery fluid. The insect desperately swims around the circular brim to find a path to escape. In doing so, it tries to grasp the clavateshaped stigmatic appendages - a futile effort, given that the appendages are slippery and curved inwards. The hairs on the inner walls of the cup, the stigmatic appendages, and the inner rows of stamens with their unique shape and structure act as insect-retaining mechanisms. The wet wings and body parts make swimming, flying or climbing up the anthers even more difficult and the insect finally succumbs (Supplementary Movie 1)." (p. 2)

      "We observed this phenomenon with no other variety of N. nouchali and N. rubra Roxb. ex Andrews growing in the same pond." (p. 3)

      "Nutrients are absorbed after the flowers are submerged, possibly to support fruit or seedling development." (p. 3)

      "Two features, namely the stigmatic cup functioning as a trap for insects and the insects being digested in the submerged flowers, distinguish this form of insectivory from the rest." (p. 3)

      "In brief, the study suggests that the insects are trapped through aquaplaning. The stigmatic cup functions like a pit trap. The flowers selectively trap flies, honeybees, and solitary bees. The form of insectivory seems primitive, given the simple mechanisms for luring, trapping, and killing followed by digestion in submerged flowers." (p. 3)

      "The process is unique, found neither in the other species of the genus Nymphaea nor in other groups of plants." (p. 3)

      "Field work was conducted in an artificial pond located in the premises of the Naoroji Godrej Centre for Plant Research, near Pune, India, where two species of water lilies (N. nouchali and N. rubra) are being cultivated." (p. 4)

      "Preliminary experiments on insecticidal properties of the liquid collected from the stigmatic cup showed 40% mortality in houseflies." (p. 4)

    Attachments

    • Snapshot
    • Tetali et al_2008_Selective insectivory in Nymphaea nouchali Burm.pdf
  • Sustainable Production of Aquatic and Wetland Plants

    Type Book Section
    Author Zane S. Coles
    Author Namrita Lall
    Edition 2
    Publisher CRC Press
    ISBN 978-0-429-42909-5
    Date 2020
    Extra 00000 Num Pages: 39
    Abstract Wetlands most often support a rich biodiversity, well beyond their direct area, and provide significant ecological and socio-economic benefits. Benefits include improving/maintaining water quality by reducing pollutants and bio-conservation of soil, water, and biological diversity that reside in or migrate through these ecosystems. This displays the vast array of benefits provided by wetlands as hydrological systems, beyond their inherent ability to improve water quality, and the need to conserve them. In addition to wild collection of species possessing traditional/medicinal properties, placing further pressure on these habitats, these ecosystems are already threatened due to urbanization, agriculture, and mining. On the other hand, the medicinal use of wetland species may provide opportunity to conserve wetland ecosystems through the enrichment of ecological awareness and the need for sustainable utilization (in situ conservation) and ex situ cultivation/conservation. Due to the growing understanding and utilization of natural products, it is necessary that desired species be propagated and cultivated as to reduce pressure on natural ecosystems. Therefore, in the interest of wetland ecosystems and the biodiversity they support, it is necessary to inform readers of suitable propagation and cultivation practices for the regeneration and production of desired species with significant potential. Beyond the commercial production of these species, this information may facilitate sustainable rural development while reducing the exploitation of natural habitats and conserving biodiversity.
    Book Title Aquatic Plants
    Date Added 11/17/2021, 2:34:23 PM
    Modified 1/23/2022, 9:49:30 PM

    Tags:

    • review

    Notes:

    • Extracted Annotations (1/23/2022, 10:02:15 PM)

      "Therefore, under cultivation, fertilization for submerged species growth must should involve the application of low quantities of ammonium salts (such as ammonium sulfate, at a rate of 2 mg/l), which are less susceptible to degradation in the sediment. These salts are less conducive to algal growth and toxicity toward the propagation plants. Emergent and foating species, on the other hand, are less affected by water clarity and can, therefore, be fertilized suffciently and directly to water." (p. 13)

      "Furthermore, inorganic carbon, necessary for submerged species, may be added through potassium bicarbonate along with other essential nutrients, including calcium, sodium, and magnesium (Smart and Barko 1984)." (p. 13)

      "Van Der Walt (2018) recommended a growth medium of equal parts of red sand-clay-loam and compost, fertilized with bonemeal." (p. 14)

    Attachments

    • Coles_Lall_2020_Sustainable Production of Aquatic and Wetland Plants.pdf
    • table-6.2.png
  • The regeneration potential of the seed bank of an ephemeral floodplain in South Africa

    Type Journal Article
    Author Margaret A Brock
    Author K. H Rogers
    URL https://www.sciencedirect.com/science/article/pii/S030437709800062X
    Volume 61
    Issue 2
    Pages 123-135
    Publication Aquatic Botany
    ISSN 0304-3770
    Date June 1, 1998
    Extra 00123
    Journal Abbr Aquatic Botany
    DOI 10.1016/S0304-3770(98)00062-X
    Accessed 11/17/2021, 2:46:27 PM
    Library Catalog ScienceDirect
    Language en
    Abstract Germination from the seed banks of ephemeral floodplain wetlands of the Nyl River in South Africa was quantified in a glasshouse experiment to examine the potential of the seed bank for revegetation. Sediments from three sites with different wetting and drying histories (permanent, seasonal and occasional inundation) were collected in late summer after flooding and germination but before the seed bank was replenished. Samples were flooded artificially after dry, wet or wet/dry pretreatment and germination was recorded. Samples were then dried and reflooded to assess germination from the residual seed bank. All sites had a species-rich germinable seed bank. The water regime history of each site did not influence the number of species or individuals present in any trial or pretreatment. More species and individuals germinated in the first germination trial than the second. Fewer species germinated from the samples collected from above the water line than from underwater. Sixteen species (12 aquatic) and 1392 individuals germinated in the first trial. Most species from the field communities also germinated from the seed bank. Twelve species, including 2 new species, germinated from the residual seed bank. Many of the species from these wetlands have persistent seed banks with staggered germination of propagules. Species maintain themselves over space (sites), conditions (water regimes) and time (trials) by a range of life-cycle patterns. Wetland communities that depend on their seed banks for revegetation between wetting and drying events may be altered by human-induced changes to water regimes.
    Date Added 11/17/2021, 2:46:27 PM
    Modified 1/23/2022, 9:08:05 PM

    Tags:

    • germination
    • Regeneration
    • Resilience
    • Seed bank
    • Temporary wetland
    • Water regime

    Notes:

    • Annotations
      (4/8/2022, 4:40:32 PM)

      “Both Nymphaea species germinated quickly from all water-regime pretreatments and all sites to dominate the first germination event (Figs. 1 and 3). Nymphaea lotus germinated from the second trial whereas Nymphaea caerulea did not. This may indicate that N. caerulea must replenish its seed bank between germination events whereas N. lotus is a generalist with viable seeds remaining after each germination event.” (Brock and Rogers, 1998, p. 132)

    Attachments

    • Brock_Rogers_1998_The regeneration potential of the seed bank of an ephemeral floodplain in South.pdf
    • ScienceDirect Snapshot
  • The Waterlilies: A Monograph of the Genus Nymphaea

    Type Book
    Author Henry S. Conard
    URL https://archive.org/details/waterliliesmonog00conruoft/mode/2up
    Place Washington
    Publisher Carnegie Institution of Washington
    Date 1905
    Extra DOI: 10.5962/bhl.title.51290 Pages: 1-432
    Series Number 4
    Language en
    Short Title The Waterlilies
    # of Pages 432
    Date Added 12/25/2021, 10:31:12 AM
    Modified 4/17/2022, 4:29:27 AM

    Notes:

    • Beginning with Nymphaea devoniensis in 1851, a continually increasing number of forms of waterlily has become known to cultivators. (pg. 219)

      From the fragmentary nature of our knowledge it is impossible to draw any general conclusions on the laws of heredity in waterlilies. So far as we can see, some characteristics are regularly blended in the hybrid offspring, while others are carried over in toto, or even exaggerated, from one or other parent. Thus, the spotting of the calyx so characteristic of N. caerulea is not a whit diminished in N. pulcherrima and A^. Pennsyl- vania, while in both the color of petal and size, shape and number of all of the floral parts are decidedly intermediate. (pg. 222)

      In Brachyceras all known hybrids are sterile, except N. capensis x zanzibariensis raised in our botanic garden, which is highly fertile, and of which a new generation of hybrids is coming on. All of the hardy yellow hybrids are entirely sterile, and crosses of N. tetragona with Eucastalia types are also sterile ; as examples of these N. laydekeri rosea and N. pygniaea alba Marliac may be mentioned. Even N. alba x Candida is greatly enfeebled in seed-producing capacity. But N. alba and N. a. rubra, though much more distinct than the last two to the casual observer, are perfectly fertile together and have fertile progeny. N. odorata and tuberosa hybrids are not self-fertile, but can be crossed with pure species. (pg. 222-223)

      It is unfortunate that Cas- pary's extensive investigations in this line have not been formulated, but his notes, exquisite color sketches, and large collection of pressed speci- mens are preserved in the Royal Herbarium of Berlin. Among them are such crosses as N. capensis X caerulea ; N. capensis X (capensis X caerulea) ; N. caerulea x [caerulea X (capensis X caerulea)] ; N. caerulea X { caerulea X [caerulea x (capensis X caerulea) - ] } ; N. flavo-virens X [capensis X (caerulea X micrantha)] . (pg. 224)

      N. stellata X caerulea. Mentioned by Caspary (1877) as a sterile hybrid… It resembles N. caerulea very closely and is generally sterile, though Caspary succeeded in fertilizing it with pollen of other individuals of the same stock and generation, and obtained a second generation of hybrids. (pg 225)

      N. caerulea X zanzibariensis (=A7. Pennsylvania Conard 1901 b)… Sterile. (pg. 225-226)

    • For cultural purposes we may divide the genus into two groups the hardy and the tender varieties. In the first group Castalia stands alone. All others are tender in our climate. (pg. 236)

      The care of them is very simple. The pond or tank may be only a large bucket or a half-barrel ; in such accommodations N. tetragona, N. t. helvola, N. marliacea chromatella, or even N. caerulea, will get along and bloom ; the first two will do quite well. But the best thing is a brick and cement pool 60 cm. deep and of as large a size as one can get room for ; after one season's trial the tank will seem too small, at any rate. A single course of brick will be sufficient for a small tank, but a double course is better. (pg. 236-237)

      Waterlilies are usually but little shaded in their native haunts, and the tropical species need all the light possible when in our northern climes. It is desirable to have the water-level constant, and to change the water just enough to keep it fresh. (pg. 237)

      The character of the soil for these pots or tubs is of prime impor- tance ; it must be very rich. Various prescriptions for its preparation have been given. R. Miiller (1885) recommends a mixture of three parts soil, two parts compost, and two parts peat for hardy Nymphaeas. We find nothing equal to well-rotted cow manure for fertilizer, and Mr. Tricker's (1897) preparation of good garden soil or sod compost with one-third to one-half of manure gives the finest possible results. Swamp muck is not at all to be recommended. If well-rotted cow manure can not be had, bone dust may be substituted in the proportion of "a six-inch pot full to a barrow load of soil " (Tricker, 1. c). Even in such strong materials a good plant of any of the larger tender forms will completely exhaust the nutriment in a half-barrel of soil before the end of the season ; hence the desirability of larger tubs for the best results. (pg. 237-238)

      The plants should be placed with the crown on a level with the surface of the soil. This should be covered with 1 to 3 cm. of clean sand to keep the manure down and to prevent the activities of certain aquatic worms which often carry up much fine matter to the surface of the tub and tend to bury the plant. For the hardy varieties the tub must be placed deep enough in the water to be safe from actually freezing. Tender varieties need to be within 15 to 25 cm. of the water surface in order to take advantage of the greater warmth of the upper strata. (pg. 238)

      Hardy species should not be moved for two or three years at least, but the tender ones must be wintered with considerable care. Large blooming plants may be lifted with a ball of earth 30 to 60 cm. in diameter, potted, and kept in a warm tank with plenty of light. They will then bloom all winter, and may be planted out again. It is best, however, to let old plants of the tender day-blooming species die. (pg. 238)

      With tender day-blooming species (apocarpous) it is important to obtain two or more plants in the spring. One of these should be kept in a 6-inch or 8-inch pot, and dried off about mid-summer to form a tuber for the next season, as the flowering plants usually die. (pg. 239)

      Propagation by seed is also easy, but is not possible for hybrids. The ripening fruits are covered with muslin bags ; the mouth of the bag is tied fast around the peduncle, and the bag should also be tied to a stick for safe keeping. After the fruit has burst and its parts decayed, the bag is taken in and the seeds washed from the debris. (pg. 239)

      Seeds of the Castalia group must be kept in water in a cool place until ready for sowing. Other seed may be dried and kept in the usual way. (pg. 239)

      The tender varieties may be sown in flat pans, barely covered with sand, and placed in warm tanks in February. The young plants should be pricked off into small pots and kept moving rapidly ; they will produce plants of the largest size the first season. Planting out in the pond must be delayed until all danger of frost, or even of a cold rain storm, is over. (pg. 239)

      The flower to be used for seed should be covered with a fine net (finer than mosquito bar) before it begins to open ; do it on the previous day. As soon as it opens (or before) all of the stamens must be plucked out. For the greatest accuracy the pollen flower should also be kept netted before and after it opens ; this is to avoid any mixing of pollen by insects. Now, on the day the seed-flower first opens, the net is removed for a moment while, with a brush, pollen from the chosen male parent is stirred around in the stigmatic fluid. The net is replaced, and in a week or so the result will be indicated by a swelling of the ovary if successful, or by decay of the flower and peduncle if no fertilization was effected… I have succeeded very well in the Brachyceras group at that time or earlier, but have no successful experience in any other group. (pg. 239-240)

      Several enemies attack waterlilies and work great havoc. In the seed beds, algae may grow up and choke the little plants ; the use of less manure and more sand in the pots is a preventive measure, and weak Bordeaux mixture will kill the algae. After the first transplanting, a damping-off fungus sometimes carries off numbers of seedlings ; the leaves become transparent in ever-increasing areas until they are all gone. This must be prevented by care in pricking off; if the plants are not wounded, and are not weakened by the shock of moving, they will outstrip the fungus. Snails, too, sometimes devour the leaves, or cut them off and leave them floating on the tank ; pick out the offenders and throw them away. The first floating leaves are often seriously weakened by swarms of aphides. A strong spray from hose or syringe will wash them off, and a few sun-fish or paradise fish will effectually prevent their return to the leaves. (pg. 240)

      Nymphaeas are also subject to a fungous disease, a leaf spot which is easily dis- cerned after a spell of warm humid weather. After such a spell of weather, followed by bright sunshine, the leaves are scorched and crumpled up, and as a result, the plant is sadly crippled by being denuded of its foliage; new leaves are weak and smaller, and so too are the flowers, if indeed there are any. This disease must be checked at once or thr plants will be severely set back, if not ruined. The only remedy is Bordeaux mixture, or any of the various mixtures with sulphate of copper as the basis. Use a fine spray, and dilute the mixture to half the strength recommended for most plants. It is best to spray twice with a weak solution rather than to spray once with too strong a solution and damage the foliage. (pg. 241)

      Finally, the ravages of muskrats eating the rhizomes of hardy species in winter must be mentioned. (pg. 241)

    • The name of this species has had a varied application, as is shown by the synonymy of this and the preceding and following plants. The cause lies partly in the close resemblance of N. caerulea and N. stellata, and partly in the fact that these and N. capensis were introduced into cultivation near the same time, and the descriptive character of the name caerulea made it equally applicable to all. The geographical prox- imity of this and N. capensis may have added to the confusion. Indeed, examination of herbarium material shows that N. caerulea is connected by intermediate forms with N. micrantha on the west and N. capensis on the south. We have not been able to secure living material of N. micrantha, but the capensis type is very easily distinguished from the present species. Their hybrid (N. pulcherrima Tricker) is entirely sterile. Other related forms are discussed in their proper places. Many botanists have included all the blue waterlilies of Africa and Asia under the name of N. stellata, as did Hooker & Thorns. (1855) ; Caspary, ten years later, separated off N. capensis, and in 1877 gave exact descriptions of four species in parallel columns; he stated that his old arrangement (1865) needed complete revision, but unfortunately this work was left undone.

    • The number of petals varies from 7 (A 7 ", tetragona) to 33 (Al. capensis). The 4 outermost are largest and alternate with the sepals ; over each interval between these, i. e., opposite each sepal, is a pair of smaller petals, making a whorl of 8. This seems to be followed in Brachyceras and Lotos by another alternating whorl of 8. Of this row usually only 4 or 5 are present in N. caerulea, while an additional row is found more or less complete in N. capensis and zanzibariensis. (pg. 80)

      In old flowers of N. caerulea, long after in- florescence, when the organs are spread apart by the growth of the ripening ovary, I have several times found the stamens arranged in 16 vertical lines, with mostly 4 stamens in each line. (pg. 80)

      They vary in number inversely as the size. N. flava may have only seven perfect seeds to a fruit, or one to three per carpel ; N. tuberosa has sixty to seventy, while N. lotus, rubra, caerulea, capensis, zanzibariensis, and amazonum have thousands. They are nearly globular in N. flava, flavo-virens, elegans, and amazonium, and ellipsoid in the rest. (pg. 90)

      The aril which is attached to the ripe seed is a bell-shaped outgrowth of the funiculus. It is whitish and translucent, mucilaginous, and holds between its two coats tiny air bubbles. It is much shorter than the seed in N. tuberosa, a little longer than the seed in N. odorata (Fig. 41, a), lotus, caerulea, capensis, zanzibariensis, and amazonum, but in these the seed is visible at the open end of the aril. (pg. 90)

      The aril serves, by its mucilage and inclosed air, to float the seed for a short time ; it drops the seed in the course of a few hours (JV. tuberosd) or a day or so {N. caerulea), partly by being bursted and torn through absorption of water, partly by decay (Fig. 41, b). (pg. 91)

      (2) Bare, with longitudinal ridges ; adjacent edges of rows of cells are alternately raised up or level ; the ridges may be interrupted at middle of seed (N. rubra (Fig. 42, a), pubescens). (pg. 92)

      (3) The seed bears longitudinal rows of hairs in the position of the ridges of the second type ; the rows may be similarly interrupted (A 7 , blanda, amazonum, gigantea, caerulea, stellata (Fig. 42, c), capensis, ampla, madagascariensis); N. lotus, thermalis, and dentata are only slightly hairy and show transitions to the second type. (pg. 92)

      Nine-tenths of the space of the seed is occupied by perisperm (nucellar tissue). This consists of large, thin-walled polyhedral cells (Fig. 44, p), densely packed with starch. (pg. 93)

      In the micropylar end of the seed a small lenticular or globose space (Fig. 44) is occupied by the endosperm and embryo. The former is a single layer of cubical cells (e) inclosing the latter. The endosperm cells are thin-walled, but Weberbauer was able to find the walls covered with pits so that the thicker portions formed a fine network. They have moderate nuclei, and contain a rich supply of proteids and oil, but no starch. Over the radicle the endosperm is very thin and poor in contents. The embryo has two equal, fleshy, hemispherical cotyledons, ex- cavated on the inner side to receive the plumule. Between their symmetrical bases is the tiny caulicle, and a slight prominence at the end of this is the radicle. Food- storing tissue of isodiametric cells and elongated conducting cells are distinguishable ; an axial strand of the latter is found in the caulicle, with a branch into each cotyledon. No starch is found in the embryo, but it is richly supplied in all its parts with oil and protein. (pg. 94)

      The formation of the principal air-canals takes place at an extremely early period. The first beginning of separation of the cells was seen in N. caerulea in a rudiment 0.5 mm. long. (pg. 96)

      Seeds of the Lotos and Brachyceras group can with- stand a great deal of drought ; they are accustomed to it ; but they are kept much more successfully, as Caspary (1877) recommended, packed in clay and air dried. Under these conditions a considerable amount of moisture is retained, even when the mass appears to be perfectly dry. (pg. 106)

      In the Dreer Gardens at Riverton, N. J., I have seen flowering plants of N, caerulea which came up spontaneously out of doors where two years previously that species had been grown ; the seeds had lain dormant over all one summer. In this case Mr. Tricker informed me that the bottom of the pond had been dug over each spring. Probably the seeds were buried in the first digging and brought to the surface in the second. (pg. 106)

      The cotyledons remain permanently within the seed and show no changes in the inner parts except in the emptying of the cells. It is by the elongation of the bases of the cotyledons into a kind of petioles that the radicle and plumule are passively carried out of the seed. These coty- ledonary petioles also curve geotropically downward until the caulicle is in a vertical position, and then they cease to grow (Fig. 49, 3, 4). Through all this time the plumule and radicle have remained dormant, but now both start into activity, the former very rapidly. The hypocotyl does not elongate at all. The epicotyl and first leaf shoot upward as a slender subulate body (Fig. 49, 3, 4). The elongation of the epicotyl depends upon the depth to which the seeds are buried ; it reaches up just to the surface of the soil. If they are uncovered at the bottom of the water, the epicotyl is scarcely visible (Fig. 49, 3) ; it is about as long as the width of the cotyledonary petioles. In other circumstances this inter- node may be 2.5 cm. long (2, 4, 5). The stimulus which effects this difference is light. (pg. 107-109)

      It will be recalled that root-hairs are generally said to be wholly lacking in Nymphaea, Nuphar, Euryale, and Victoria. As we have observed them in N. dentata, lotus, caerulea, zanzibariensis, amazonum, elegans, odorata, capensis, and hybrids, they are doubtless universal in the genus. On one occasion also they were found on early roots of a plant springing from a tuber of N. caerulea. (pg. 111)

      The nutritive relations of waterlilies have not been specially worked out. They require a large amount of nitrogenous food, as every cultivator can testify, but prefer it in the form of nitrates rather than ammonia. Excess of calcium, as in limestone waters, is not beneficial. Doubtless these substances are absorbed with water by the roots directly, since no root-hairs are present. And the importance of the roots is shown by the great reduction in vigor of plants when moved from one pot to another, though they soon regain their strength. (pg. 116)

      A peculiar adaptation occurs, on the other hand, in plants of any species, when grown in very shallow water, say 10 to 15 cm. This often occurs in our gardens, where we have the tropical kinds as near to the surface as possible in order to keep them warm. Now, the flower bud is first pushed out from the apex of the plant in a very immature state, and it is to finish its development as it is rising through the water. In very shallow water, therefore, it reaches the surface when it is by no means ready to be exposed to the air. The situation is recognized at once by the plant, and the peduncle bends to one side and becomes S-shaped (Fig. 52) ; thus the bud maintains its erect position and is kept submerged. Then in due time, the bud having matured and the peduncle having reached a suitable length, the latter straightens up and lifts the former into the proper position for opening. (pg. 118-119)

      The process of opening and closing usually occupies nearly an hour. On its first day the flower always opens about an hour later than on subsequent days, closes earlier, and spreads but half as wide.

      7-8 am N. caerulea, marliacea chromatella, and tuberosa open.

      12-1 pm N. odorata, tuberosa, caerulea, and elegans close.

      The stimulus to these actions is to be attributed, in diurnal species at least, wholly to light… That light is the normal stimulus is also shown by the earlier opening of the flowers in more northern latitudes. (pg. 120)

      The large and showy flowers of waterlilies are in many ways designed for the visits of insects. The colors are mostly conspicuous and attractive. N. caerulea is comparatively insignificant ; and N. rubra makes very little showing at night, but in the early morning it is magnificent. (pg. 121)

      The flowers are always pistillate on the first day of opening, and the stigmatic cup is filled nearly to overflowing with a large quantity of slightly sweetened water. This is excreted by the stigma itself and by the axile process. The stamens at this time stand erect around the stigma, leaving a narrow vertical pit in the center of the flower, bounded all over the sides by the still closed anthers of stamens of different lengths. (pg. 121)

      In Brachyceras, as a rule, the entrance to the pistil is totally obstructed on the second day by the inner stamens, and the outer ones are dehiscing ; subsequently the inner stamens bend outward and dehisce until, on the last day, the passage to the stigma is wide open again. In spite of this, N. caerulea and stellata are said by Caspary (1877) to be capable of self-pollination, the latter while still in the bud. The stiff stamens of the- Lotos group dehisce simultaneously on the second day, and undergo no considerable change of position. (pg. 122)

      In Lotos and Brachyceras also the flower often sinks while still open, but on its last day it has already moved down near to the water surface, and is not totally submerged until 1 2 to 20 hours later. The submergence of the flower is due to active, even power- ful, movements of the peduncle, and occurs most pronouncedly in fertilized flowers. Infertile flowers scarcely get below the surface of the water, and then quickly disintegrate ; sometimes the peduncle decays before the floral parts, showing how great is the transmitted effect of fertilization. (pg. 123)

      Under the most favorable circumstances only about half of the ovules proceed with development to form mature seeds, but the presence of 10 or 12 fer- tile ovules in each cell of such fecund species as N. lotus or caerulea is suffi- cient to stimulate the movements of the peduncle. (pg. 123)

      In N. amazonum there is a double curve, so that the ripening fruit is upright. But in other species more or less of spiral coiling accom- panies the bending. The stout peduncles of Brachyceras descend in the same manner as N. amazonum, but there is in addition a strong curving of the lower half of the peduncle to the right or left. The result is that we find the fruits near the bottom of the water, 15 to 35 cm. away from the crown of the plant and on the opposite side from the point of insertion of the fruit-stalk. (pg. 123)

      In deep water (1 to 5 meters) N. flava, odorata, alba, and tuberosa carry the spiral turning to its highest development. From a few centimeters above the rhizome to within a few centimeters of the flower, the peduncle is coiled into a close helix from 2 to 8 centimeters in diameter, and with 2 to 8 or 10 turns ; thus the fruit is drawn down within about half a meter of the bottom of the water, and often quite into the mass of algae and other vegetation overlying the mud. (pg. 124)

      Besides removing the fruit from the drying influence of the air, the purpose of these movements is doubtless twofold : First, to hide the fruit from the many aerial, aquatic, and amphibious animals which might feed upon it, for the majority of such creatures get their food at the surface rather than in the depths of the water ; secondly, to reduce the danger of the fruits being broken off, as would easily occur with the long, slender peduncles of Castalia. (pg. 124)

      • Carpels free at sides, i. e., walls between ovary cells double (Fig. 40) (Nymphaeae apocarpiae)
      • 1. Carpellary styles present, thick and fleshy ; stamens appendaged (Brachyceras)
      • 2. Flowers never yellow
      • 4. Leaves entire or nearly so
      • 5. Leaves ovate or orbicular
      • 6. African species
      • 7. Not bulbilliferous
      • 8. Leaves green or purplish-green beneath , spotted with black
      • 9. Petals 14 to 20 ; stamens 50 to 75 (pg. 126)

    Attachments

    • Conard_1905_The waterlilies.pdf
    • Details - The waterlilies: a monograph of the genus Nymphaea - Biodiversity Heritage Library
    • fig-44-seed-diagram.png
    • plate-8-nymphaea-caerulea.png
  • Transcultural use of narcotic water lilies in ancient egyptian and maya drug ritual

    Type Journal Article
    Author William A. Emboden
    URL https://www.sciencedirect.com/science/article/pii/0378874181900131
    Volume 3
    Issue 1
    Pages 39-83
    Publication Journal of Ethnopharmacology
    ISSN 0378-8741
    Date 1981-01-01
    Journal Abbr Journal of Ethnopharmacology
    DOI 10.1016/0378-8741(81)90013-1
    Accessed 4/6/2022, 3:08:06 PM
    Library Catalog ScienceDirect
    Language en
    Abstract Comparisons are made between ancient ritual uses of the flowers of Nymphaea (Nymphaeaceae) in Maya and Egyptian civilizations. Recurrent motifs encountered in the art of both of these ancient civilizations suggests that the role of the water lily was that of a narcotic (psychodysleptic) used to mediate ecstasis among a priestly caste. Relevant literature is reviewed as are chemical data. Elements in the complex belief systems of these two civilizations need to be reinterpreted in view of the use of two water lilies as ritual narcotics. The species implicated are Nymphaea caerulea Sav., in Egypt, and N. ampla DC., among the Maya.
    Date Added 4/6/2022, 3:08:06 PM
    Modified 4/6/2022, 3:08:06 PM

    Notes:

    • Annotations
      (4/6/2022, 4:20:53 PM)

      “The genus Nelumbo (syn. Nelubium) was unknown in ancient Egypt and was never found as a part of ancient monuments or of any art.” (Emboden, 1981, p. 40)

      “In 1877 Caspary, working on collections made by Sieber in Damietta, Egypt, recognized that N. caerulea var. albiflora was the plant that Kotschy had identified as N. amplu. The mistake is explained in part by the observation that N. caerulea hybridizes with N. micrantha to the west, and N. capensis to the south.” (Emboden, 1981, p. 40)

      “Many botanists such as Hooker and Thompson (1855) found it convenient to treat all blue water lilies of Africa and Asia as N. stellata.” (Emboden, 1981, p. 40)

      “Hybridization within the genus is common and has added another dimension of confusion; however, hybridization does not occur between Old World and New World species.” (Emboden, 1981, p. 41)

      “The first reference to narcotic properties comes from an 1822 report made by Descourtilz, a doctor of medicine of the University of Paris. In the eighth volume of his Flora Pittoresque et Me’dicinale des Antilles he writes (on page 266) that a doctor named Ailbert assured him that he had used “Nymphoea” as a narcotic to replace opiates. He utilized the flowers and the fruits.” (Emboden, 1981, p. 53)

      “The species of Nymphaea was never stated and has been taken to be N. alba which is abundant in that area.” (Emboden, 1981, p. 53)

      “Descourtilz is explicit in saying the “roots” (that is to say, the rhizome) were not used.” (Emboden, 1981, p. 53)

      “The next important report comes from Pobeguin (1912) who in writing of Nymphaea stellata and N. caerulea (the two have often been confused - even by botanists) states, “ La decoction de la fleur est narcotique.. .” This is the first published instance in which the blue water lily of ancient Egypt is implicated in a narcosis which involves the use of the flower.” (Emboden, 1981, p. 53)

      “In 1909 Stuhlmann pointed out that the rhizomes of Nymphaea caerulea while eaten when cooked, were “poisonous” unless boiled.” (Emboden, 1981, p. 53)

      “Delphaut and Balansard (1941) in that year published thei” (Emboden, 1981, p. 53)

      “Arguments that Nymphaea caerulea was only an ornamental plant must recognize that the flower opens only for four hours, from 8 a.m. until noon, and then promptly closes. For this reason, it is not particularly suited as an ornament. Moreover, the closed flowers have no fragrance.” (Emboden, 1981, p. 20)

      “Dobkin de Rios (1974) wrote about the toad motif (Bufo) as an element in the psychotropic fauna of the Maya, and found a high frequency of this representation combined with Nymphaeu amplu.” (Emboden, 1981, p. 61)

      “Emboden’s (1974) suggestion of possible narcotic properties of N. amplu led her to formulate her hypothesis (1977a and b) that the role of the white water lily was of importance in Maya thought and that if used by the priests it might have considerable impact on their cosmological concepts by altering their sense of time. This she suggests is through the action of apomorphine acting as a strong emetic.” (Emboden, 1981, p. 61)

      “Such published errors, supplemented by a full-page photograph, tend to enter as an erroneous part of the lore surrounding the water lily. It is clear that no botanist was consulted in making this incorrect assertion.” (Emboden, 1981, p. 25)

    Attachments

    • Emboden_1981_Transcultural use of narcotic water lilies in ancient egyptian and maya drug.pdf
    • ScienceDirect Snapshot