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Article

Diversity, Ecological and Traditional Knowledge of Pteridophytes in the Western Himalayas

1
Department of Life Science, Glocal University, Saharanpur 247121, India
2
Clybay Research Private Limited, Bangalore 560114, India
3
Department of Ethnobotany, Institute of Botany, Ilia State University, 0105 Tbilisi, Georgia
4
Department of Botany, University of Gujrat, Hafiz Hayat Campus, Gujrat 50700, Pakistan
5
Department of Botany, University of Okara, Okara 56130, Pakistan
6
Zonal Educational Office, Vehil, Shopian, Jammu & Kashmir 192303, India
7
Prince Sultan Bin Abdulaziz International Prize for Water Chair, Prince Sultan Institute for Environmental, Water and Desert Research, King Saud University, Riyadh 11451, Saudi Arabia
8
Department of Agricultural Engineering, College of Food and Agriculture Sciences, King Saud University, Riyadh 11451, Saudi Arabia
9
Plant Production Department, College of Food & Agriculture Sciences, King Saud University, Riyadh 11451, Saudi Arabia
10
Floriculture, Ornamental Horticulture, and Garden Design Department, Faculty of Agriculture (El-Shatby), Alexandria University, Alexandria 21545, Egypt
11
Department of Geography, Environmental Management, and Energy Studies, University of Johannesburg, APK Campus, Johannesburg 2006, South Africa
12
Department of Life Sciences, Yeungnam University, Gyeongsan 38541, Korea
*
Author to whom correspondence should be addressed.
These authors contributed equally to this work.
Diversity 2022, 14(8), 628; https://doi.org/10.3390/d14080628
Submission received: 22 June 2022 / Revised: 11 July 2022 / Accepted: 3 August 2022 / Published: 6 August 2022
(This article belongs to the Special Issue Diversity in 2022)

Abstract

:
Pteridophytes have been used by humans for millennia, but in comparison to flowering plants, the documentation of their traditional uses is still neglected; as a result, they must be highlighted and popularized. The present study was carried out from January 2019 to November 2021 to gather ecological and traditional use information on pteridophytes from local inhabitants of the Kashmir valley via semi-structured personal interviews and group discussions. We recorded 58 pteridophyte species belonging to 13 families. The distributions of the species among the families were unequal, with four families constituting more than half of the total species (Dryopteridaceae 26%, Woodsiaceae 17%, Aspleniaceae 14%, and Pteridaceae (14%). The highest numbers of species (45%) were found growing on the forest floor, followed by those growing in rock crevices (26%). This was supported further by a cluster analysis, which identified two primary clusters based on the species presence in different habitats. Half of the species (56%) were reported from altitudes below 2000m, followed by 19% from 2001–2500m, and 8% (e.g., Deparia allantodioides, Dryopteris xanthomelas, Asplenium viride) from 3001–3500m. Among the documented species (N = 58), only 28 species had a traditional usage (as medicine, vegetables, for oral hygiene, and for veterinary use). The aerial parts were most commonly used (64%) followed by the rachis (18%). The highest use value was observed for Diplazium maximum and the lowest for Asplenium fontanum. The findings of our study contribute baseline data to fill the existing knowledge gaps on ecological and traditional knowledge of pteridophytes in the Himalayas.

1. Introduction

Pteridophytes are a plant group that falls between non-tracheophytes and spermatophytes and account for over 48 families, 587 genera, and 12000 species worldwide [1,2,3]. The richness of the species is affected by the rainfall, moisture, and habitat availability [4]. Most species are found in tropical and moist temperate regions followed by subtropical regions [5]. They are widely utilized as vegetables, traditional remedies, and for land scaping and gardening [6]. Proteins, vitamins, crude fiber, and minerals are all found in edible pteridophytes, and steroids, terpenoids, phenolic acids, and flavonoids are only a few of the compounds found in them [7].
Pteridophytes were considered a source of medicines in ancient times but remain relatively under explored. However, fern ethnobotany is not new [8], and there is a wealth of information regarding ferns and local cultures in the literature. On a global scale, [8] offered the most thorough analysis of the usage of lycophytes and ferns, but they have also been studied ethnobotanically in South America [9]. Asia has a great diversity of pteridophytes, but their uses have not been well recorded except for a few studies in China and India [10,11].
The Kashmir valley is an integral but geologically younger part of the Himalayan range [12]. Due to topographical, altitudinal, and geographical variation, the valley represents a vast habitat diversity and floristic richness, which is of immense scientific interest and economic potential [13]. The available scientific literature on the flora of the valley indicates that while phanerogams are well documented, little attention has been paid to pteridophytes [12]. Nevertheless, the earliest reported study of the pterido-flora of Kashmir dates back to 1880 [14], and other studies include those found in [15,16,17,18,19,20,21,22,23,24,25,26,27,28]. The valley is inhabited by diverse ethnic people with unique living patterns, and most people reside in rural areas and possess a strong relationship with the natural resources. This relationship with nature has been documented [29,30,31,32].
However, the research on pteridophytes still focuses on taxonomy [12,25,26,27,28] and there are no available studies on traditional use. A few scattered reports are available for ferns and fern-allies from other regions [26,27,28,29]. The present study was designed not only to assess the medicinal importance of pteridophytes but also other uses by the indigenous people, highlighting their economic potential for the area under study. In this regard, the present study aimed:
To document the pteridophyte species with ethno-usage;
To evaluate the ecological knowledge of the local inhabitants of the Kashmir valley regarding the pteridophytes;
To analyze the further distribution of species at different altitudes.

2. Materials and Methods

2.1. Study Area

Kupwara (Figure 1) is a frontier area in the Union territory of Kashmir, which is mainly mountainous with rich flora. The region covers an area of 2379 km2 and this area is mostly rural, including 368 villages with a population of 870,354 persons and a population density of 366 persons/km2 [33].The area is very biodiverse, with dense forests (Himalayan dry-temperate to subalpine forest types) [34]. The climate is of the dfb type, with temperatures falling below −4 °C in winters and reaching 32 °C maximum in summer [35].

2.2. Survey Methodology

The present study was carried out from January 2019 to November 2021 to gather traditional use reports and ecological information of pteridophytes from the local inhabitants. Ecological data were collected along the altitudinal gradient from 1500–3450 m. During the surveys, data pertaining to the field-based ecological knowledge—such as habitat types of each of the documented species—was collected [36]. The different habitat types included forest floor, rock crevices, grassland pastures, moist paces, and riparian [37]. The ethnobiological information was gathered through semi-structured interviews and group discussions [38,39]. Before interviews, verbal prior informed consent was obtained, and the code of ethics was followed in all aspects of the study (International Society of Ethnobiology. Code of Ethics. 2006) (https://www.ethnobiology.net) (accessed on 28 August 2020). All information was obtained in local language by hiring a translator and local field guide.

2.3. Preservation and Identification of Collected Plants:

The specimens collected from the field were shade-dried and processed into herbarium specimens following standard techniques [40]. The identification was performed with the assistance of Prof. S.P. Kullar (Chandigarh) and Mr. C.R. Fraser-Jenkins (Portugal). Herbarium specimens were deposited in the Department of Taxonomy, University of Kashmir, for future references. The botanical names of the plant species were verified using the Plant List (www.theplantlist.org) (accessed on 28 August 2020. A comparative literature review was conducted to evaluate the possible novelty of the findings.

2.4. Demography of Informants

A total of 58 local individuals, comprising 39 (67.24%) men and 19 (32.75%) women, were selected for the interviews. Due to cultural limitations, the number of male respondents was higher [41,42,43]. Most of the respondents were illiterate (65.51%). Older people (55.17%) had greater traditional knowledge compared to the young (10.34%). The respondents belonged to a variety of professions among which shepherds were the most common (36.20%), followed by skilled laborers (24.13%), farmers (22.41%), and housewives (17.24%) (Table 1).

2.5. Data Analysis

For the dendrogram, presence/absence of data was used to elucidate species distribution in particular clusters based on the same habitat type [44]. The Sorensen’s (Bray–Curtis) distance was used to identify significant differences among diverse habitat types and plant resemblances using Past software ver. 3.14 [45]. A Kernel density map was prepared using ARCGISver.10.5. This depicts hotspots in the landscape, with the darker red color indicating greater species number. We used absence/presence data to depict the distribution of the species on the heat map, and the subsequent cluster analysis will combine species with comparable altitudinal ranges. The program “circlize package” [46] was used to construct chord diagrams in R software 4.0.0. [47]. This graph allows us to see which species in each group and which altitude group has the greatest number of species based on the thickness of each bar [39].

3. Results and Discussions

3.1. Taxonomic Composition

During the present study, we recorded 58 pteridophyte species belonging to 13 families (Figure 2a). The current documentation is the first of its kind from the valley, as no such study related to pteridophytes has been carried out in the region as per our knowledge. Irfan et al [48], who reported 168 taxa belonging to 45 genera and 19 families from Pakistan, Rajput et al. [49] reported 23 species from Gujrat India, Uday et al. [50] reported 77 species belonging to 15 families from Jhargram district of southwest Bengal, and Bibi et al. [51] reported 45 species belonging to 10 families from Ghar KP, Pakistan.
The distribution of species (Figure 3) in the families was unequal, with four families constituting more than half of the total species (Dryopteridaceae (N = 14), Woodsiaceae, Aspleniaceae, and Pteridaceae (N = 8 each). The family species relationship (y = 13.732e−0.219xR² = 0.923) can be observed (Figure 2b). Our results are similar to Bibi et al. [51], who also reported Dryopteridaceae as the dominant family while evaluating the diversity from Ghar, KP, Pakistan; likewise, Irfan et al. [52] reported Dryopteridaceae as the dominant family from Battargam, KP, Pakistan. Gul et al. [53] also reported Dryopteridaceae as the leading family from Pakistan. Our inventory of the documented flora including the scientific name, local name, family, attitude, habitat, and the 11 villages is presented in Table 2. Among all the study sites, most of the species were reported from Thandipora (31%), followed by Rashanpora-Dutt (14%) and Budnamal (10%) (Table 2).

3.2. Ecological Knowledge

We found that the local people possessed profound ecological knowledge about fern species, e.g., their habitats and altitudinal distribution. The habitats included forest floors, rock cervices, grass land pastures, moist places, and riparian areas. The highest number of species (45%) was found on the forest floor, followed by rock crevices (26%), grassland pastures (17%), moist places (7%), and riparian zones (5%) (Table 2). This was further supported by a cluster analysis in which two primary clusters were recorded (Figure 4): Cluster one included the forest floor, comprising species such as, Asplenium adiantum, Pteridium brownseyi, Dryopteris juxtaposita, and Cluster two included grass land pastures with species such as Pteridium revolutum, Dryopteris barbigera, Dryopteris blanfordii, as well as moist paces with Asplenium dalhousia and Equisetum arvense and riparian zones harboring Marsilea minuta and Salvinia natans. Our results are a similar to Bibi et al. [51] from Pakistan, Arjun et al. [54] from Kerala, and Suneetha et al. [55] from Madhya Pradesh.
More than half of the species (56%), including Pteris cretica, Adiantum tibeticum, Adiantum venustum, and Adiantum capillus-veneris, were reported from altitudes below 2000 m, 19% from 2001–2500 m (e.g., Asplenium fontanum, Thelypteris microstegia, Deparia japonica, Deparia petersenii), 17% of the species (e.g., Athyrium dubium, Lepisorus clathratus) from 2501–3000 m, and 8% (e.g., Deparia allantodioides, Dryopteris xanthomelas, Asplenium viride) from 3001–3500 m (Figure 5). A circular layout of the diagram represents the documented species and altitudinal ranges, and its inner lines represent the relationship between the species and altitude. The lines connecting each species and altitude represent their importance in relation to each other, and the size of the arc reflects the number of species in each category. The histogram illustrates the number of species in the landscape, with the greater species numbers (32) in the lower (below 2000 m) altitudes (Figure 6). When comparing the upper and middle altitudinal regions, the lower areas had higher species numbers. This may be due to the fact that a lower altitude provides diverse, suitable habitats for the growth of pteridophytes.

3.3. Traditional Knowledge

The use of ferns in ethnomedicine has been studied on all inhabited continents, including the Americas and Europe [8]. However, current and updated information on the medical applications offered in Asia and Africa is not easily available. In Asian traditional medicine, pteridophytes are an important category of plants. Mannan et al. [56] Discussed their applications in homeopathic, ayurvedic, tribal, and Unani medicine. Indian pteridophytes have been widely explored for their ethnomedicinal usage [57]. However, no extensive study has been carried out in the Kashmir Himalaya to document the pteridophyte species with ethno-usage.
Among all the documented species (N = 58), only 28 species were recorded for ethno-usage (Table 2). Our results are inline with Sarker et al. [58] reported the ethno-use of pteridophytes from the mensingh district of Bangladesh, Khullar [5] Dehradun, India, and Lie et al. [59,60] from China. We classified the traditional uses into four categories (Medicine, vegetable, oral hygiene and veterinary use) (Figure 7a), among which veterinary use was dominant (N = 9), followed by medicine (N = 8), vegetable (N = 6), and oral hygiene (N = 6) (Figure 5a). Species such as Dryopteris barbigera, Dryopteris blanfordii, Dryopteris juxtaposita, Dryopteris redactopinnata, and Polystichum discretum were the main species used for ethno-veterinary purposes. The species with medicinal attributions included Asplenium adiantum-nigrum, Asplenium ceterach and Asplenium trichomanes. For oral hygiene, the species employed were Asplenium trichomanes, Equisetum arvense, and Equisetum diffusum. Pteridium brownseyi, Pteridium revolutum, Dryopteris ramose, were used as vegetables. According to [61], eating ferns has a 3000-year history in China, and edible ferns are among the most commonly harvested wild food plants in the world, with the stems, rhizomes, leaves, young fronds, and shoots, as well as whole plants, being utilized for food [62]. Although ferns have long been utilized in traditional cuisines, there is a scarcity of knowledge of their usage patterns, nutritional characteristics, and recipes, and generally ferns are rarely used as a food source, with a few exceptions [56]. It is important to mention that the young fronds of Pteridium revolutum and the aerial parts Dryopteris stewartii are only eaten when boiled first and then properly sun-dried, because the local users know that if they are taken while green, they may cause cancer and vomiting. The dominance of veterinary usage is because the local people employ the maximum documented species as strays for stables (Figure 7) of the domesticated fauna such as goat, sheep, cow, and buffalo. The complete ethno-usage of the documented species is provided in Table 2.
The aerial parts of ferns were most commonly used (64%), followed by rachis (18%), young fronds (11%), rhizomes (4%), and roots (3%) (Figure 6b). Giri et al. [61] reported the dominance of aerial parts (the whole plant) in ethno-usage from India; Joshi et al. [63] also reported the dominance of aerial parts (whole plant) from India. The use value ranged between 0.29–0.69 (Table 2): the highest use value was observed for Diplazium maximum and the lowest for Asplenium fontanum. The high UV value for Diplazium maximum was due to its high edible value, with local people consuming it as vegetable. The season for collections runs from March to May, and the collected species is sun dried and made into powder, stored, and used in winters. The local people believed that the species enhances one’s life span, explaining its common use. During harsh winters, the availability of green leafy vegetables is sparse, and the price is also very high in local markets, resulting in the dependence of the local people on wild collected vegetables such as Diplazium maximum. Further, some tribal people collected the Diplazium maximum for commercial purposes. The women from these tribes travel to far off places to sell the collected species and earn decent profits in return. Joshi et al, Shrestha et al. [64,65] reported the commercial value of Diplazium species from Central Nepal. Diplazium is commonly known as the fiddle head fern, including edible species such as Diplazium esculentum, Diplazium sammatii, and Diplazium proliferum. The genus is known to have a unique omega 6 fatty acid (di-homo-gammalinolenic acid) as well as polyphenols, suggesting its possible function as a nutraceutical [7]. According to [7], different leafy vegetables such as Amaranthus, asparagus, celery, spinach, and lettuce are inferior in nutritional quality to ferns.

3.4. Toxicity

In the present study, the local people indicated that certain potentially poisonous ferns (Asplenium dalhousia, Pteridium brownseyi, Pteridium revolutum, Dryopteris barbigera, Dryopteris blanfordii, Dryopteris juxtaposita, Dryopteris nigropaleacea, Dryopteris ramosa, Dryopteris stewartii, Athyrium mackinnoniorum, Polystichum discretum, Polystichum aculeatum, Polystichum squarrosum, Polystichum lonchitis, Polystichum piceopaleaceum, Polystichum prescottianum, and Polystichum yunnanense) are not poisonous if harvested at the inappropriate stage. These potentially toxic species constitute 31.03% of the total documented species and are often the cause of livestock deaths. The toxicity of the plant/part can be ascribed to the alkaloids present at the armature stage.The authorof [66] reported livestock deaths from Indonesia due to plant toxicity.
The existence of rare fern species (Polystichum aculeatum, Pteris vittata, Lepisorus nudus, Ophioglossum reticulatum, Polystichum prescottianum, Pteridium brownseyi, and Dryopteris juxtaposita), which were reported for the first time from this part of the Kashmir Himalayas, was one of this study’s most intriguing findings. Polystichum aculeatum was recently reported from Kashmir Himalayas by [66].

4. Conclusions

The current research is the first comprehensive examination of the ecological and traditional uses of pteridophytes in the study area. We documented 58 pteridophyte species, with Dryopteridaceae being the most common. Most species were found at lower elevations (below 2000m). Among the total number of species reported, 28 species had traditional uses. Veterinary uses were the most common, followed by medical and vegetable uses. Diplazium maximum is a highly-edible species that the locals most commonly eat as a vegetable. Due to an ever-changing physical environment, increasing population pressure, and rapid socio-economic growth, all of these species and their related traditional knowledge are endangered. Since much of the information is still in the hands of the local community without any written documentation, the collection and documentation of such information is critical. Ethnopteridological knowledge needs to be efficiently collected, conserved, and used to benefit the country’s development and conservation.

Author Contributions

Data collection A.A.K.; Data Analysis S.M.H., M.M. and M.W.; Initial original draft S.M.H., M.H., U.Y.: Revision, A.A.K., A.Z.D., M.A.-Y., A.A.; W.Z., H.O.E., K.Y., M.M., U.Y., S.M.H., R.W.B. and M.H., A.A.K., A.Z.D., M.A.-Y., H.O.E., K.Y.; Review, R.W.B. and W.Z. All authors have read and agreed to the published version of the manuscript.

Funding

This research was financially supported by the Deanship of Scientific Research, king Saud University through Vice Deanship of Scientific Research Chairs; Research Chair of Prince Sultan Bin Abdulaziz International Prize for Water.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

All the participants provided prior informed consent before interviews; also ethnobiology code of ethics was followed (https://www.ethnobiology.net/what-we-do/core-programs/ise-ethics-program/code-of-ethics/).

Data Availability Statement

All data obtained during the study is included in this article.

Acknowledgments

The authors extend their appreciation to the Deanship of Scientific Research, King Saud University for funding through Vice Deanship of Scientific Research Chairs; Research Chair of Prince Sultan Bin Abdulaziz International Prize for Water.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. (a) Map of India, (b) map of Jammu and Kashmir, (c) map showing surveyed villages in the District of Kupwara, and (d) Kernel density map of the sampled villages.
Figure 1. (a) Map of India, (b) map of Jammu and Kashmir, (c) map showing surveyed villages in the District of Kupwara, and (d) Kernel density map of the sampled villages.
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Figure 2. (a) Percentage of families; (b) species–family relationship of the documented species in the study area.
Figure 2. (a) Percentage of families; (b) species–family relationship of the documented species in the study area.
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Figure 3. Representation of the species collected during the field study. (P.C. Aadil Abdullah Khoja).
Figure 3. Representation of the species collected during the field study. (P.C. Aadil Abdullah Khoja).
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Figure 4. Clustering of documented species in different habitat in the study area.
Figure 4. Clustering of documented species in different habitat in the study area.
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Figure 5. Percentage of species found in different altitudinal groups in the study area. The direction of the lines shows which species is associated with which type of altitudinal group, and the thickness of each bar shows the number of species in each altitudinal type. The complete name of each species is shown in Table 2.
Figure 5. Percentage of species found in different altitudinal groups in the study area. The direction of the lines shows which species is associated with which type of altitudinal group, and the thickness of each bar shows the number of species in each altitudinal type. The complete name of each species is shown in Table 2.
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Figure 6. Altitudinal variations of the documented species in the study area.
Figure 6. Altitudinal variations of the documented species in the study area.
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Figure 7. (a) Different uses of documented species; (b) Percentage of different parts of the documented species for the tradition uses.
Figure 7. (a) Different uses of documented species; (b) Percentage of different parts of the documented species for the tradition uses.
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Table 1. Demography of informants from the study area.
Table 1. Demography of informants from the study area.
InformantsNumberPercentage
Total58100
Men3967.24
Women 1932.75
Age groups
Young 25–40 years610.34
Middle aged 41–55 years2034.48
Old aged 56–75 years3255.17
Occupation
Shepherds2136.20
Farmers1322.41
Skilled laborers1424.13
Housewives1017.24
Education
Illiterate3865.51
Primary1322.41
Secondary712.06
Table 2. Inventory of the documented species from the administrative Kupwara district of Jammu and Kashmir.
Table 2. Inventory of the documented species from the administrative Kupwara district of Jammu and Kashmir.
FamilyBotanical Name/Voucher No.Local NameVillageAltitudeHabitatToxicityPart UsedEthno-UseUse Value
AspleniaceaeAsplenium adiantum-nigrum L.
Asp adi
KUP-001
GuewtheerThandipora1900Forest floor×Areal partUsed to treat jaundice0.63
Asplenium ceterach L.
KUP-002
Asp cet
ReachThandipora1900Rock crevice×Areal partUsed to treat kidney stones0.33
Asplenium fontanum (L.) Bernh. subsp. pseudofontanum
KUP-003
Asp fon
Sheen-ghassBudnamal2500Rock crevice×Areal partUsed to treat respiratory diseases0.29
Asplenium dalhousiae Hook.
KUP-007
Asp dal
Thandipora1900Moist places
Asplenium laciniatum D. Donsubsp. laciniatum
KUP-008
Asp lac
Keran2500Rock crevice
Asplenium septentrionale (L.) Hoffm.
KUP-004
Asp sep
Rashanpora Dutt3100Rock crevice×
Asplenium trichomanes L.
KUP-005
Asp tri
GuewtheerThandipora1950Rock crevice×Areal partUsed to treat Jaundice0.34
RachisUsed as toothpick.
Employed after ear piercing for a week before use of earrings.
0.50
Asplenium viride Huds.
KUP-006
Asp vir
LakitguewtheerChowkibal2200Rock crevice×FrondUsed to treat sun burns0.36
AzollaceaeAzolla filiculoides Lam. subsp. cristata
KUP-009
Azo fil
Lolab1600Riparian zone×
CystopteridaceaeCystopteris fragilis L.
KUP-047
Cysfra
Thandipora1950Rock crevice×
Cystopteris fragilis nonthosubsp. x montserratti Prado and Salvo
KUP-048
Cysfra
Marsari1900Rock crevice×
DennstaediaceaePteridium brownseyi Fraser-Jenk.
KUP-010
Pte bro
LongudSatboin2500Forest floor×Young frondUsed as vegetable0.53
Pteridium revolutum Blume
KUP-011
Pte rev
LongudSadnatop2800Grassland pasturesYoung frondUsed as vegetable and for Asthma0.60
DryopteridaceaeDryopteris barbigera T. Moore ex Hook.
KUP-012
Dry bar
Kaw-deadRashanpora Dutt3000Grassland pasturesAreal partUsed as bedding for livestock during winters0.41
Dryopteris blanfordii C. Hope
KUP-013
Dry bla
Hapat-daedRashanpora Dutt3000Grassland pasturesAreal partUsed as bedding for livestock during winters0.38
Dryopteris juxtaposita Christ.
KUP-014
Dry jux
Hapat-daedFarkan1900Forest floorAreal partUsed as bedding for livestock during winters0.40
Dryopteris nigropaleacea (Fraser-Jenk.) Fraser-Jenk.
KUP-015
Dry nig
Farkan2000Forest floor
Dryopteris ramosa (C.Hope) C. Chr.
KUP-016
Dry ram
DeadFarkan1900Forest floorAreal partUsed as vegetable0.48
Dryopteris redactopinnata S.K. Basuand Panigrahi
KUP-017
Dry red
Kaw-daedBudnamal2500Forest floor×Areal partUsed as bedding for livestock during winters0.36
Dryopteris stewartii Fraser-Jenk.
KUP-018
Dry ste
Kaw-daedFarkan1900Forest floorAreal partUsed as vegetable0.43
Dryopteris xanthomelas (Christ) C. Chr.
KUP-019
Dry xan
Sadnatop2400Forest floor×
Polystichum aculeatum L.
4246-KASH
Pol acu
Kaw-daedFarkan1950Forest floorAreal partUsed as bedding for livestock during winters0.45
Polystichum discretum (D. Don) J. Smith
KUP-020
Pol dis
Kaw-daedFarkan1950Forest floorAreal partUsed as bedding for livestock during winters0.39
Polystichum lonchitis (L.) Roth
KU-023
Pol lon
Bungus valley3100Forest floor
Polystichum piceopaleaceum Tagawa
KUP-024
Pol pic
Hapat-daedThandipora1950Forest floorAreal partUsed as bedding for livestock during winters0.46
Polystichum squarrosum D. Don.
KUP-022
Pol squ
Jungle-daedThandipora1950Forest floorAreal partVegetable
Polystichum yunnanense Christ.
KUP-026
Pol yun
Thandipora1950Forest floor
EquisetiaceaeEquisetum arvense L.
4232-KASH
Equarv
GandamgudThandipora1900Moist areas×RachisUsed for cleaning teeth0.65
Equisetum diffusum D. Don
4233-KASH
Equdif
GandamgudThandipora1900Moist areas×RachisUsed for cleaning teeth0.60
Equisetum ramosissimum Desf.
KUP-027
Equ ram
Thandipora1900Rock crevice×
MarsileaceaeMarsilea minuta L.
KUP-028
Mar min
PafluSat-boin1600Riparian zone×RhizomeDiuretic0.43
OsmundaceaeOsmunda claytoniana L.
KUP-029
Osmcla
MubrakhgulRashanpora Dutt3000Grassland pastures×Areal partUsed as bedding for livestock during winters0.33
OphioglossaceaeOphioglossum reticulatum L.
KUP-030
Oph ret
Chan-choorThandipora1950Grassland pastures×RootsUsed as wound-healing agent0.45
PolypodiaceaeLepisorus clathratus (C.B. Clarke) Ching
KUP-031
Lepcla
Rashanpora Dutt3100Rock crevice×
Lepisorus nudus (Hook.) Ching,
KUP-032
Lepnud
Rashanpora Dutt3100Rock crevice×
PteridaceaeAdiantum capillus-veneris L.
4115-KASH
Adi cap
GuewtheerThandipora1900Forest floor×RachisUsed as toothpick.
Employed after ear piercing for a week before use of earrings.
0.55
Adiantum venustum D. Don.
4104-KASH
Adiven
GuewtheerMarsari1900Forest floor×RachisUsed as toothpick.
Employed after ear piercing for a week before use of earrings.
0.57
Adiantum tibeticum Chingand Y.X. Lin.
KUP-033
Adi tib
GuewtheerThandipora1900Forest floor×RachisUsed as toothpick.
Employed after ear piercing for a week before use of earrings.
0.53
Cryptogramma brunoniana Wall. ex Hook.
KUP-034
Cry bru
Chowkibal2000Rock crevice×
Cryptogramma stelleri (S.G. Gmel.) Prantl
KUP-035
Cry ste
Budnamal2500Rock crevice×
Onychium cryptogrammoides Christ
KUP-036
Ony cry
Thandipora2000Grassland pastures×
Pteris cretica L.
KUP-037
Pte cre
Jungle-daedThandipora1900Forest floor×Areal partUsed as wound-healing agent0.45
Pteris vittata L.
KUP-038
Pte vit
Satboin1600Forest floor×
SalviniaceaeSalvinia natans L.
KUP-039
Sal nat
Satboin1600Riparian zone×
ThelypteridaceaeThelypteris levingei Clarke Ching
KUP-040
The lev
Marsari1900Forest floor×
Thelypteris microstegia subsp. microstegia E.W. Trotter and Hope
KUP-041
The mic
Budnamal2500Forest floor×
Thelypteris microstegia subsp. laterepens (E.W. Trotter) Fraser-Jenk.
KUP-042
The mic
Budnamal2500Forest floor×
Thelypteris palustris Schott
KUP-043
The pal
Thandipora1950Rock crevice×
Phegopteris connectilis (Michx.) Watt
KUP-044
Phe con
Bungus valley2550Moist areas×
WoodsiaceaeAthyrium attenuatum (C.B. Clarke)
KUP-062
Ath att
Bungus valley2550Grassland pastures×
Athyrium dubium Ching
KUP-046
Ath dub
Rashanpora Dutt3000Grassland pastures×
Athyrium mackinnoniorum (C. Hope) C. Chr.
KUP-045
Ath mac
DaedThandipora1950Forest floorAreal partUsed as Vegetable0.36
Deparia allantodioides (Bedd.) M. Kato
KUP-049
Dep all
Budnamal2400Forest floor×
Deparia japonica Thunb.
KUP-050
Dep jap
Sadnatop2800Forest floor×
Deparia petersenii Kunze
KUP-051
Dep pet
Sadnatop2800Grassland pastures×
Diplazium maximum (D. Don) C. Christ
KUP-052
Dip max
LongudMarsari2000Forest floor×Areal partUsed as vegetable0.69
Gymnocarpium fedtschenkoanum Pojark.
KUP-053
Gym fed
Chowkibal2100Rock crevice×
× (presence of toxicity); √ (absence of toxicity).
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Khoja, A.A.; Haq, S.M.; Majeed, M.; Hassan, M.; Waheed, M.; Yaqoob, U.; Bussmann, R.W.; Alataway, A.; Dewidar, A.Z.; Al-Yafrsi, M.; et al. Diversity, Ecological and Traditional Knowledge of Pteridophytes in the Western Himalayas. Diversity 2022, 14, 628. https://doi.org/10.3390/d14080628

AMA Style

Khoja AA, Haq SM, Majeed M, Hassan M, Waheed M, Yaqoob U, Bussmann RW, Alataway A, Dewidar AZ, Al-Yafrsi M, et al. Diversity, Ecological and Traditional Knowledge of Pteridophytes in the Western Himalayas. Diversity. 2022; 14(8):628. https://doi.org/10.3390/d14080628

Chicago/Turabian Style

Khoja, Aadil Abdullah, Shiekh Marifatul Haq, Muhammad Majeed, Musheerul Hassan, Muhammad Waheed, Umer Yaqoob, Rainer W. Bussmann, Abed Alataway, Ahmed Z. Dewidar, Mohamed Al-Yafrsi, and et al. 2022. "Diversity, Ecological and Traditional Knowledge of Pteridophytes in the Western Himalayas" Diversity 14, no. 8: 628. https://doi.org/10.3390/d14080628

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