Research Article |
Corresponding author: Anjula Pandey ( anjuravinder@yahoo.com ) Corresponding author: Pavan Kumar Malav ( pavan.malav@icar.gov.in ) Academic editor: Lorenzo Peruzzi
© 2021 Anjula Pandey, K. Madhav Rai, Pavan Kumar Malav, S. Rajkumar.
This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Citation:
Pandey A, Rai KM, Malav PK, Rajkumar S (2021) Allium negianum (Amaryllidaceae): a new species under subg. Rhizirideum from Uttarakhand Himalaya, India. PhytoKeys 183: 77-93. https://doi.org/10.3897/phytokeys.183.65433
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A new species, Allium negianum (Amaryllidaceae), belongs to the genus Allium subg. Rhizirideum, sect. Eduardia is described here from the Uttarakhand Himalayan region of India. This taxon grows in Malari region of Niti valley in Chamoli district and Dharma valley of Pithoragarh district, Uttarakhand, India. It is a narrowly distributed species and morphologically more closer to A. przewalskianum Regel but differentiated by its tunic color of bulb, umbel with lax flowers, peduncle length, perigone colour, size and shape and leaf anatomy. Taxonomic delineation and relationship analysis based on nuclear ribosomal Internal Transcribed Spacers (ITS) region indicated that A. negianum is distinct and related to A. przewalskianum. This study provided a comprehensive description and comparison with A. przewalskianum, an identification key and notes on the distribution of the species.
Allium negianum, India, Rhizirideum, Seasoning spice, Uttarakhand
Allium L., one of the largest genera in the family Amaryllidaceae, has about 1,100 species distributed world-wide (
Globally Allium subg. Rhizirideum (G.Don ex Koch) Wendelbo s.str. has ca. 37 taxa that are included in four sections distributed mainly in Europe-East Asia, in China (
Taxa of the subg. Rhizirideum belong to the third and the most advanced evolutionary line, which is phylogenetically sister to taxa of the subg. Allium L., Cepa L., Reticulatobulbosa (Kamelin) N.Friesen and Polyprason Radic. (
Despite the importance of the genus Allium for the Indian region, meagre comprehensive studies have been attempted pertaining to molecular and taxonomic evaluation that led to gaps in the status of interspecific and infraspecific relationships among the taxa. Meagre taxonomic studies on the native taxa, unavailability of material for research, sporadic collections from under-explored/unexplored areas and lack of the published literature have led to the possibility of finding new taxonomic records from the Indian region (
The subg. Rhizirideum is the smallest subgenus of Allium as per the flora of India, and it is represented only by the sect. Eduardia containing only one species, A. przewalskianum Regel. This taxon occurs in the scrub, drier slopes, ravines and rocky crevices (2000–4500 m a.s.l.) in Leh, Jammu and Kashmir and Spiti in Himachal Pradesh. The taxa under subg. Rhizirideum are characterized by the presence of several narrowly ovoid-cylindric bulbs, which borne on creeping rhizome usually covered with a common reticulate membrane, leaves shorter than scape, adaxially channeled and stamens slightly longer than perigone segments, spathe with a long beak, nearly 2 to 3 times longer than the base and hemispherical umbel. Most species share a basic chromosome number of x = 8 and 2n = 16 or 32. Occurrence of a polyploid complex in different sections of the subgenus Rhizirideum indicated recent origin of taxa as supported by phylogenetic and biogeographical evidences (
A new taxon, Allium negianum, was collected from the Indo-Tibetan border area of Malari village, Niti valley of Chamoli district in Uttarakhand (India) in 2019 and identity was confirmed by the authors. It is distinct from its closest relative, A. przewalskianum Regel (Table
A total of 110 plants representing 7 accessions of the new species were collected from the type locality and farmers’ fields in the Niti region of Uttarakhand, India. For delimitation of the taxon with other related species, plants were grown in the Field Gene Bank (FGB) at the ICAR-National Bureau of Plant Genetic Resources (ICAR-NBPGR), Regional Station Bhowali (Nainital), Uttarakhand for comparative study of morphological characters. Data were recorded using the Allium descriptor with modifications from the published literature. The floral characters were measured with separate parts to the nearest ten points of the decimal. The seeds having uniform size and maturity were recorded for ultra-features of the characters using the Stereozoom Microscope (LMI, England, model no. SZM167), and the images were captured as JPEG. Ten replicate voucher herbarium specimens of the new species were prepared as per standard procedure and deposited in the National Herbarium of Cultivated Plants (code-NHCP) (Holotype) and CAL (Isotype).
The new species was compared with its closest relative using data derived from the study of specimens preserved in the herbaria of CAL, DD, E, K and NHCP and available literature. Due to its closer affinity with A. przewalskianum, all the specimens from diverse sources were critically examined. Taxonomic description and identification key were provided for Allium negianum and affined species.
For leaf anatomy live plants were grown in the FGB at Regional Station Bhowali (Nainital), Uttarakhand. Leaf-blades were taken from a point 3–4 cm above the sheaths and fixed in 70% alcohol. Cross-sections were made at three different lengths of leaf and stained with Sartur solution (a mix of sudan III, aniline, chloral hydrate, lactic acid, iodine), the structure was studied, and analyzed with the help of a light microscope (Olympus BH-2) and line diagrammes drawn. The outlines of cells were diagrammatically depicted (Fig.
Allium negianum A general habitat B bulb covered with reticulate fiber on bulbs of A. przewalskianum (orange-red) and A. negianum (red-brown) C inflorescence and spathe with a very long beak, persistent D inflorescence E capsule with mature seeds F line-illustrations of transverse section of leaf showing hollow channel G longitudinal section of flower with stamen with two sharp teeth H ovary I seed with prominent beak (C–I magnification × 30–40).
Genomic DNA of nine known species and one new taxon (Table
S. no. | Taxon name | Subgenus | Section | NGB accession number | District; state |
---|---|---|---|---|---|
1 | Allium tuberosum Rottler ex Spreng. | Butomissa | Butomissa | IC353524 | Almora; Uttarakhand |
2 | Allium stracheyi Baker | Polyprason | Orioprasum | IC567645 | Pithoragarh; Uttarakhand |
3 | Allium przewalskianum Regel | Rhizirideum | Eduardia | IC632207 | Leh; Jammu and Kashmir |
4 | Allium negianum sp. nov. | Rhizirideum | Eduardia | IC258493 | Chamoli; Uttarakhand |
5 | Allium sativum L. | Allium | Allium | IC278243 | Chamoli; Uttarakhand |
6 | Allium ampeloprasum var. ampeloprasum | Allium | Allium | IC353526 | Pithoragarh; Uttarakhand |
7 | Allium cepa var. cepa L. | Cepa | Cepa | IC410711 | Uttarkashi; Uttarakhand |
8 | Allium cepa L. var. aggregatum G.Don | Cepa | Cepa | AP/RP/2014 | Chamoli; Uttarakhand |
9 | Allium oschaninii O.Fedtsch. | Cepa | Cepa | AP/2014 | Voucher; Uttarakhand |
10 | Allium schoenoprasum L. | Cepa | Schoenoprasum | IC632213 | Kargil; Jammu and Kashmir |
Major morphological characters* (discriminating characters in bold) of Allium negianum in comparison with A. przewalskianum.
Character | A. przewalskianum | A. negianum |
---|---|---|
Habitat | Carbonaceous slates-gravel; 3300–5200 m | Grassy meadows, open sandy slopes, along rivers/ streams; 3000–4800 m |
Plant habit | Erect | Semi-erect |
Plant growth (under experimental condition) | Robust, shorter | Taller, plants and leaves |
Plant height (cm) | 20–45 | 27–50 |
Bulbs no. in cluster | 2–4 | 2–7 |
Bulb no., shape | Cluster 3–4; cylindrical-narrowly ovoid | Cluster 4–8; cylindrical-narrowly ovoid |
Bulb length (cm) | 10.2–12.5 | 6.8–12 |
Bulb diameter (cm) | 0.6–0.7 | 0.8–1.2 |
Tunic outer** | Finely reticulate; reddish-orange-brown | Finely reticulate; reddish-dark brown |
Tunic inner | Membranous, brown-red | Membranous, orange-red |
Rhizome type; size (mm) | Vertical, short; 3–5 | Oblique; 7–12 |
Leaf no., colour | 3–5, lighter brown-green | 4–6, dark green |
Leaf vs. scape | Much shorter than scape | Slightly shorter than scape |
Leaf blade shape; apex | Linear, not fistular; obtuse to subrounded | Linear, filiform; acute |
Leaf length (cm) | 15–30 | 12–40 |
Leaf width (mm) | 2.0–2.5 | 1–3.2 |
Leaf erectness | Erect | Erect-semierect |
Leaf waxiness | Non-waxy | Waxy |
Leaf cross section | Circular | Circular |
Spathe valve if persistent | 1(2)-valved, persistent | 1-valved, persistent |
Spathe valve shape, size | Ovate | Ovate-oblong |
Spathe size (cm) | 2–3 (two times the base; short, blunt) | 4–6 (long narrow beak; 3 times the base) |
Scape type | Solid, terete, erect, central | Solid, terete, erect to semi-erect, lateral-central |
Scape size (cm) | 30–40 × 0.2–0.35 | 20–50 × 0.36–0.48; 1/3-of the base |
Pedicel vs. perigone | Subequal | 2–3 times longer |
Umbel flower opening pattern |
Synchronous (80 per cent) |
Asynchronous (30–40 per cent) |
Umbel shape | Spherical-hemispherical, densely flowered, compact | Hemispherical, lax, loosely flowered |
Umbel diameter (mm) | 28.5–30.2 | 25.1–42.0 |
Umbel flower (no.) | 25–40 | 30–40 |
Peduncle size (cm) | 0.5–1.0 | 0.8–2.5 |
Flower size (cm) | 0.4–0.5×0.3 | 0.5–0.5× 0.4 |
Flower color | Pale red-purple pink (variable) | Dark purple (as recorded now) |
Perigonium shape and color | Campanulate, pink-dark purple, tepal wide open | Campanulate, lilac, light to dark purple, tepal partly opened |
Tepal shape | Ovate-lanceolate, apex obtuse | Elliptic, ovate-lanceolate; apex-acuminate-mucronate |
Tepal inner size length × width (cm) |
0.3–0.4 ×0.2–0.3 | 0.5–0.6 × 0.3–0.4 |
Tepal outer size length × width (cm) |
0.5–0.7 × 0.2–0.3 | 0.6–0.7 × 0.3–0.5 |
Tepal apex shape | Acute-acuminate | Acute, mucronate |
Tepal maturity | Curved outwards | Slightly inwardly curved/rolled |
Tepal mid-vein | Non-conspicuous; purple green-dark purple | Very conspicuous; green-light green |
Anther length (mm) | 6.1–9.3 | 6.8–8.5 |
Anther lobe length (mm) | Oblong-ovate, 1–2 | Oblong, 1–2 |
Anther lobe color | Yellow-purple | Yellow-purple |
Filament color | Yellowish-purple | Greenish yellow-purplish green |
Filament length, position | Double the size of tepal; exserted, | Half the size of tepal; slightly exerted |
Filament inner and outer anther | Inner – two sharp teeth up to 1/2 to 1/4 length of filament with broader base; outer narrower base | Inner – two shallower-sharper teeth up to 1/2 to 2/3 length of filament with base as wide as tepal; outer narrower base |
Ovary shape | Ovoid – globose, wrinkled | Obovoid – subglobose |
Ovary color | Purple green, tinged with purple | Dark-pale purple |
Ovary style vs. anther (after pollination) | Much exserted, longer than the ovary | Slightly exserted or equal |
Ovary stigma tip | Acuminate-acute | Acuminate |
Stigma vs. stamen | Sub-equal | Slightly longer |
Capsule shape | Ovoid | Sub-globose |
Seed length (mm) | 2.75–2.96 | 3.21–4.05 |
Seed width (mm) | 1.55–1.59 | 1.92–1.97 |
Seed color | Dull black | Shiny black |
Seed no./locule | 2 | 2 |
1000 seed wt (g) | 2.12 | 2.73 |
Odour when crushed# | Strong onion-light garlic | Strong onion-garlic |
The generated DNA sequences from both the primers were checked for alignment using the BioEdit software. Multiple pairwise alignments of generated sequences and from NCBI database were made using ClustalW. The aligned sequences were used to generate the genetic distance between taxa and the evolutionary history, which was inferred by using the Maximum Likelihood method based on the Jukes-Cantor model using MEGA7.0 (
India, Uttarakhand: Chamoli, rocky areas (altitude 3000–4800 m), 22 Aug. 2019, KMR/AS/02/19 (Holotype: NHCP; Isotype: CAL; Seeds conserved in the National Genebank, New Delhi: IC258493).
Herbs, hermaphrodite, 27–50 cm tall. Rhizome condensed, 6.5–8.5 mm long, oblique. Bulb clustered, cylindric to narrowly ovoid, 0.8–1.2 cm in diameter, 6.8–12 cm long, outer tunic finely reticulate, reddish-dark brown, inner membranous, light-brick red. Leaves 4–6, slightly shorter than scape, 12–40 cm × 1.0–3.2 mm, erect, to semi-terete to terete, dark green; base slightly bulbous. Scape terete, semi-erect, covered with leaf sheaths at base only, stout, solid in cross-section (hollow in mature), 15–30 cm × 3.5–5.5 mm. Spathe 1-valved, persistent, beak very narrow-long, 2.5–4 mm. Inflorescence umbellate, hemispheric, 30–40 lax flowered. Peduncle subequal, 16–18 × 2–3 mm, without bulbils. Flowers bisexual, perigone campanulate, tepals dark purple with distinct green mid-line; inner tepals slightly longer than outer ones, oblong-lanceolate, apex acute, 6–8 × 3–4 mm; outer segments ovate to narrowly so, 5.5–6 × 2.5–3 mm. Stamens anthers oblong, yellow-purplish (on maturity), 2.3–2.6 mm long; filaments subequal, 6.8–8.5 mm, purple, slightly exserted, connate at base and adnate to perigone segments; outer ones subulate; inner ones broadened for 1/2–1/4 to their length, one sharp toothed on each side. Ovary sub-globose, purple-tinged, 3.6–4.8 × 1.8–3.5 mm. Style terete, exserted, stigma smooth, acute-acuminate, ovules 2 per locule. Capsules trigonous, 5–5.5 × 5.8–7.2 mm; seeds obovate with a prominent notch on one side, 3.2–4.0 × 1.9–1.9 mm, testa deep black. Plant has strong onion-garlic type aroma.
Slopes, sandy soils along rivers and streams along the alpine meadows (altitude 3000–4800 m asl) in Sumna valley (villages Gamsali, Niti, Tolma, Kailashpur and Farkya) in Chamoli district near Malari glacier of India.
The specific epithet, “negianum”, is named in honour of Late Dr. Kuldeep Singh Negi, an eminent explorer who has dedicated his life in collection of indigenous Allium species germplasm along with associated indigenous knowledge across the country. He was also instrumental in establishing the Allium Field Gene Bank (FGB) at the Regional Station, Bhowali, Uttarakhand. The entire germplasm of indigenous Allium species collected by him from remote areas of the country are characterized and successfully conserved at Allium FGB, Bhowali, Uttarakhand.
Pharan, phran, jambu, sakua, sungdung, kacho, etc. (
Flowering and fruiting is from June to middle September (altitude 3000–4800 m a.s.l.).
The transverse section of the leaf of A. negianum showed an elliptical outline. The epidermis has small cells covered with a thin cuticle layer, and stomata are narrowly distributed along the surface area. Single layered compactly arranged palisade tissue comprised of long cylindrical cells. The mesophyll cells are spongy tissue and compact in young leaf as well in the proximal ends of mature leaf while in the centre part of mature leaf, broken mesophyll cells are confused with fistulous leaf appearance; 10–12 vascular bundles are arranged along with the palisade tissue across the entire circumference (Fig.
Seed characters and testa sculptures represents a good taxonomic character in Allium (
The testa cell shape was irregularly hexagonal-pentagonal, loose with clear meshes of reticulated tissue. The anticlinal walls are usually raised, prominently small to intermediate granulose verrucae. The periclinal cells wall has several verrucae with irregular depressions. Study indicated that in subg. Rhizirideum testa cell shape varied from oval to irregular or oval to hemispherical; and seed length 1.30–2.35 mm, anticlinal wall were distinguished by nearly S type to straight and periclinal wall was flat to nearly convex with densely granulated verrucae (
The sect. Eduardia of the subg. Rhizirideum is distributed in the southern most range of the Himalayan region of India extending to China which is the centre of diversification. Allium negianum is a species recorded from the southernmost transitional zone between India and China. The distribution of A. negianum is restricted to the phytogeographical region of western Himalaya from Sumna valley, Malari, Chamoli district of Uttarakhand, in western Himalaya, India where it commonly occurs along the open grassy meadows, sandy soils along rivers and streams occurring in the snow pasture lands along the alpine meadows (locally known as ‘bugyal’ or ‘bugial’) between 3000–4800 m a.s.l. (Fig.
The first report on large scale cultivation of this taxon in Niti valley, Uttarakhand, as ‘seasoning allium spice’ called ‘jambu’ and ‘phran’ has been published (
(Paratypes). Allium przewalskianum: India. Himachal Pradesh. Spiti, Takcha 25 Jul. 1972 U.C. Bhattacharya 48815 (BSD); Tobo, Kinnaur, Lahul & Spity, 15 Sept. 2007, V.D. Verma & Ramchander (NHCP); Jammu & Kashmir. Ladakh, 25 July 1941, Ludlow & Sheriff8529 (BM); 8 Sep.1941, Ludlow & Sheriff8571 (BM); Ganglas, 1 Aug. 1988, H.J.Chowdhury & B.P.Uniyal 86043 (BSD); 1880, Aitchinson376 (CAL); Kashmir. Nubra, 24 July 1980, A.R. Naqshi & G.N. Dhar7370 under A. stracheyi; Leh (J&K), 8 Sept. 2014, K. Pradheep & P.S. Mehta1733 (NHCP); Leh (J&K), Nov. 2014, K.Pradheep HS21817 (NHCP); Pangu lake, Luthum village, Leh (4500 m), s.s. Malik & D. Gautam15298 (NHCP); Uttarakhand. Malari, Chamoli, 10 Sept. 2019, Badal Singh & K.Madhav RaiHS24013 (NHCP); Allium auriculatum: Uttarakhand: Brahmmathya, district Chamoli, August 1988, K.S.Negi & M.N.Kopper 9387 (NHCP).
A. stoliczki: Ladakh, Khaedubgla, 18 Aug. 1982, P.K.Hazra98623(K), 1985, Jacquemont V. Type (K); T. Thomson, Type (K); China, 1 Jan. 1872, Przewalski N.M., #s.n., Type (P); 01 Jan. 1884, Przewalski N.M., Type (P, K); 1872–1873, Przewalski N.M., #s.n., Type (G).
There are no records on the availability of this new taxon from Uttarakhand (
Allium negianum was previously mistaken for identity as A. stracheyi as noted in the published records from India. Despite no morphological similarity with the latter taxon,
Upon critical examination of specimen of A. auriculatum deposited in the NHCP, all plant characters were found to be closer to A. negianum. Four specimens of this taxon were noted in label data as frequently growing on flat rocks in Brahmmathya, district Chamoli (3800 m asl.), Uttarakhand, used as leaves cooked as a vegetable.
Allium negianum is morphologically allied to a Chinese species A. eduardi Stearn that occurs on the dry slopes and plains in the adjoining regions of Mongolia and Russia and shares characters of spathe beak size, hemispherical umbel and perigone shape, but differs in having yellowish-brown bulb tunic color, tepal apex with a reflexed point and shorter stamen teeth length.
Two species, A. przewalskianum and A. negianum, of the subg. Rhizirideum, sect. Eduardia can be distinguished from A. stracheyi of the subg. Polyprason by using the following key.
1 | Bulbs cylindrical-narrowly oblong-ovoid, outer tunic fibrous, with finely reticulate texture, reddish-dark brown, leaves semiterete-terete | 2 |
– | Bulbs cylindric-narrowly ovoid, outer tunic fibrous scarious, brown-darkest brown, leaves narrow, fistulous | A. stracheyi |
2 | Bulbs outer tunic reticulate, reddish, inner tunic membranous, red-orange, rarely light brown; umbel compact globose, tepal pale-red to dark purple; filaments longer than perigone segments, inner ones broadened for 1/3–1/2 their length with shallow teeth; style very much exserted after anthesis | A. przewalskianum |
– | Bulbs outer tunic reticulate, reddish-brown, inner tunic membranous red; umbel hemi-spherical, lax; tepals dark purple-pink purple; filaments equal to perigone segments, inner ones broadened at the base for 2/3–1/3 of length, sharply marked teeth; style slightly exserted after anthesis | A. negianum |
For taxonomic delineation and relationship analysis data set comprising 18 representative taxa from diverse subgenera were selected (Table
Sl. No. | Species | Genbank accession number |
---|---|---|
1 | Allium tuberosum Rottler ex Spreng. | MZ567234 (present study) |
2 | Allium stracheyi Baker | MZ567226 (present study) |
3 | Allium przewalskianum Regel | MZ567224 (present study) |
4 | Allium negianum sp. nov. | MZ567225 (present study) |
5 | Allium sativum L. | MZ567230 (present study) |
6 | Allium ampeloprasum L. var. ampeloprasum | MZ567231 (present study) |
7 | Allium cepa L. var. cepa | MZ567228 (present study) |
8 | Allium cepa L. var. aggregatum G.Don | MZ567232 (present study) |
9 | Allium oschaninii O.Fedtsch. | MZ567229 (present study) |
10 | Allium schoenoprasum L. | MZ567227(present study) |
11 | Allium eduardii Stearn ex Airy Shaw | MK917745 |
12 | Allium subangulatum Regel. | AJ411870 |
13 | Allium tenuissimum L. | AJ411846 |
14 | Allium nutans L. | JN864787 |
15 | Allium prostratusm Trevi. | LN867014 |
16 | Allium spurium G.Don. | LN867017 |
17 | Allium spirale Willd. | JN864784 |
18 | Allium polyrhizum Turcz. ex Regel | MK917742 |
Two major clades were found within Allium, comprising subgen. Rhizirideum, on one side and second cluster had four subg. Butomissa, Allium, Polyprason and Cepa. on the other side. This former group was divided in two sister clades, with first clade having Allium przewalskianum, Allium negianum sp. nov. A. eduardii (all from section Eduardia); Allium subangulatum, A. polyrhizum from sect. Caespitosoprason; and A. nutans, A. prostratusm, A. spurium and A. spirale in sect. Rhizirideum. One of the taxon A. tenuissimum from sect. Tenuissima grouped separately. Second clade was divided into subgenera, namely Butomissa with one taxon, Allium tuberosum; subg. Allium, with Allium sativum and Allium ampeloprasum var. ampeloprasum; subg. Polyprason having Allium stracheyi; subg. Cepa that was the largest having four taxa, Allium cepa var. cepa, A. cepa var. aggregatum, A. oschaninii and A. schoenoprasum from distinct sections.
Based on the likelihood tree, the new Allium taxon was observed to be closely related to A. przewalskianum, both of Indian Himalayan origin along with a Chinese taxon, A. eduardii to form distinct cluster supporting the morphological resemblance of this taxa with section Eduardii under subg. Rhizirideum. The species from other sections under same genus were distantly placed in the phylogenetic tree. The species which are found in same geographical area belong to different subgenera viz. Allium, Cepa, Butomissa and Polyprason were distantly placed and used as outgroup in determining the integrity of newly described species Allium negianum.
The above findings indicated that the new taxon is a distinct species and is closely related to A. przewalskianum and belongs to sect. Eduardia under subg. Rhizideum. These findings supported the observations recorded using plant morphology, particularly the floral characters that were very distinct in both the taxa.
Distribution of taxa of Allium subg. Rhizirideum sect. Eduardia in India: Allium negianum and A. przewalskianum shown by the red triangle and black circled dots respectively; blue rectangle showed the occurrence of A. przewalskianum as per the data from GBIF (records of occurrence from Uttarakhand).
Recent advances in molecular phylogenetics have revolutionized our understanding of Allium taxonomy and evolution. However, the phylogenetic relationships in some Allium sections (such as the Allium sect. Eduardia) and the genetic bases of adaptative evolution remain poorly understood for the Indian taxa (
Allium negianum, a new species under the subg. Rhizirideum, is described using live and herbarium specimens. With the inclusion of this taxon, in the subg. Rhizirideum of the sect. Eduardia there are two taxa in India, and the latter one A. negianum was reportedly restricted to the Uttarakhand flora. Samples of this taxon collected during earlier explorations that remained unidentified will be designated with this new name and conserved as seed in the National Gene Bank (NGB), New Delhi and vegetative material will be maintained in the Field Gene Bank (FGB) at Bhowali, Uttarakhand, India.
The authors are especially thankful to the Head, Division of Plant Exploration and Germplasm Collection and the Officer-in-charge, Regional Station Bhowali (Nainital), Uttarakhand to facilitate repeated surveys and field observations at the type locality under Global Environment Facility and National Exploration Plan (2019–20) programmes and for growing the germplasm. For the line diagrams help rendered by Mr. RK Pamarthi and Mr. Kunal Patil is greatly acknowledged.