Journal of Threatened Taxa | www.threatenedtaxa.org | 26 June 2020 | 12(9): 16099–16109

 

ISSN 0974-7907 (Online) | ISSN 0974-7893 (Print) 

doi: https://doi.org/10.11609/jott.4554.12.9.16099-16109

#4554 | Received 10 December 2018 | Final received 25 May 2020 | Finally accepted 01 June 2020

 

 

 

Phytodiversity of chasmophytic habitats at Olichuchattam Waterfalls, Kerala, India

 

Arun Christy 1  & Binu Thomas 2

 

1,2 Department of Botany, Centre for PG studies & Research, St. Joseph’s College (Autonomus), Devagiri, Kozhikode, Kerala 673008, India.

1 arunchristysebastian03@gmail.com, 2 binuthomasct@gmail.com (corresponding author)

 

 

 

Editor: B. Ravi Prasad Rao, Sri Krishnadevaraya University, Ananthapuramu, India.             Date of publication: 26 June 2020 (online & print)

 

Citation: Christy, A. & B. Thomas (2020). Phytodiversity of chasmophytic habitats at Olichuchattam Waterfalls, Kerala, India. Journal of Threatened Taxa 12(9): 16099–16109. https://doi.org/10.11609/jott.4554.12.9.16099-16109

 

Copyright: © Christy & Thomas 2020. Creative Commons Attribution 4.0 International License.  JoTT allows unrestricted use, reproduction, and distribution of this article in any medium by providing adequate credit to the author(s) and the source of publication.

 

Funding: None.

 

Competing interests: The authors declare no competing interests.

 

Author details: Arun Christy currently working as project fellow at Department of Botany, Maharaja’s College, Ernakulam and dealing with the lichenological studies of Kerala. The present article is based on the results of taxonomic studies carried out by him during his post graduation studies in Department of Botany, St. Joseph’s College (Autonomus). Dr. Binu Thomas currently working as Assistant professor in Department of Botany, St. Joseph’s College (Autonomus). He has authored three books, seven book chapters in edited books and more than 100 articles in various national and international Journals. He also being an active reviewer in various reputed Journals. His areas of research interests are in angiosperm taxonomy and phytochemistry.

 

Author contribution: AC—conducted the field trip, collection, Identification and compilation of various datas on chasmophytic plants in the study area. BT—planned the outline of this research work and provided necessary guidelines for the research.

 

Acknowledgements: The authors are thankful to the Principal, St. Joseph’s College, Devagiri, Kozhikode. We also acknowledged the faculty members and Research scholars of Department of Botany, St. Joseph’s College, Devagiri for their support and valuable suggestions.

 

 

Abstract: The present study was conducted to analyse the Phytodiversity of Chasmophytic habitats at Olichuchattam waterfalls, Kerala, India. The studies on the plants in such special type of habitats are very less. Hence the present study will help to know more about them. Field exploration and observations were made, plants were collected, identified and herbarium was prepared.  Analysis of plants and soil samples from different regions of the study area based on altitudinal variations was also done. As a result of the study, a total of 120 plant species that belonging to 49 families and 93 genera were documented. Of these 5 species are bryophyte, 10 species are pteridophytes and 105 species are angiosperms. The ornamental potentiality of the plants in the study area was also analysed and it shows that a total of 47 species have ornamental potentialities. The present study also highlighted some threatening factors can affect the distribution of plants in the present study area. The present study highlights that, the rocky cliffs and crevices serves as an excellent habitat for many interesting plant groups. The plants in these habitats are very unique and are attractive.The rocky cliffs and crevices represents a good indicator of rich biodiversity within small areas.

 

Keywords: Floristic diversity, chasmophytes, Olichuchattam, invasive species, threats.

 

 

 

 

 

 

 

INTRODUCTION

 

Floristic diversity refers to the variety and variability of plants in a given region.  It refers to the number of types or taxa in a given region or group.  India is one of the 12 mega diversity centres of the world where the Western Ghats and the Himalayan region constitute two of the 34 biodiversity hotspots representing a storehouse of several promising economically important plants (Myers 1990).  Species richness and endemism are, however, not uniformly distributed along the Western Ghats.  The southernmost regions which have the most favourable climatic conditions with high, but not excessive rainfall and short dry season are the ones with the highest biodiversity and contain the highest number of endemic species (Pascal et al. 2004).  Southern Western Ghats is one of the two mega endemic centres in Western Ghats (Nair & Daniel 1986; Nayar 1996).  Kerala forms a major species-rich part of southern Western Ghats harbouring a total of 4,679 flowering plants (Sasidharan 2004).

The vegetation on the surface of rocks or stones are lithophytes, while the vegetation in the crevices of rocks are chasmophytes (Schimper 1898).  Rock crevices form a major habitat for many plants and host rich biodiversity within a small area.  The rocky habitat provides an extremely harsh physical environment for plants that leads to the development of specialized plant communities with endemic and habitat specific species.  Microhabitats like rock crevices possess diverse forms of plants, which are mainly seasonal herbs.  These habitats differ from each other due to changes in geographical terrain and soil cover (Porembski 2000).

Chasmophytes are plants rooted in clefts of rocks that are filled with detritus.  In these clefts, particles of earth conveyed by wind and water accumulate.  The amount and rate of accumulation depends upon the width and situation of the clefts (Davis 1982).  The soil thus constituted facilitates plants to establish and their dead fragments further add to the supply of the nutritive material in the clefts (Bashan et al. 2002).  Rocky cliffs are microhabitats which are slightly mineral rich and can support the growth and survival of many chasmophytic species.  The occurrence of such habitats ultimately depends on a number of factors such as geographical location, levels of exposure, high evaporation rates, nature of soil geology, and water runoff during the rainy season (Danin et al. 1982).  The chasmophytic species growing on rock crevices and cliffs have to deal with an extremely inhospitable environment.  Therefore, they have developed several adjustments such as strong roots and reduced life form structure.  This root system supports them on the cliffs and allows for maximum exploitation of the little water and nutrients contained in minimal soil.  This habitat is also susceptible to strong winds and full sunlight, as there is no tall vegetation to protect it from these climatic factors (Binu & Rajendran 2012).

The growth of chasmophytic plants mainly depends on the availability of water and depth of soil with nutrients.  The number of plants is more during the wet season than during the dry season.  The rocky cliffs and crevices represent a good indicator of rich biodiversity within small areas (Binu et al. 2012).  The pioneering plants such as lichens, mosses, ferns & fern allies, small herbs, and grasses grow in the weathered soil in the rock crevices and loosen the weathered particles of rocks and add an organic material to the developing soil.  These plants trap water and wind-blown soil and can add soil content in the crevices.  Finally, dead organic matter of such a pioneer community can add more suitable substrata for the growth of the next community (Roy et al. 1983).

The objectives of the present study were: (i) to document the chasmophytic diversity of the study area, (ii) to study the various factors affecting the growth and survival of chasmophytes in the study area, and (iii) to characterize the chasmophytic plants in the study area.

 

 

MATERIALS AND METHODS

 

Study Area

The study area Olichuchattam is situated in Thiruvambady Panchayath of Kozhikode District of Kerala State, India (11.435˚N & 76.079˚E; Figure 1, Image 1).  Olichuchattam  area  comes under the jurisdiction of Vellarimala Forest Range which is a part of the Western Ghats.  Most of the hill range falls in the Meppadi Forest Range of South Wayanad Division, with some parts falling in the Thamarassery Range of Kozhikode Division (Image 2–5).  Olichuchattam is a waterfall of Iruvanji River situated in evergreen forests on the way to Vellarimala Hills.  The hill ranges are accessible on foot from Muthappanpuzha, a small town which is about 50km from Kozhikode.  By trekking for about 4–5 km (approximately three hours) one can explore the Olichuchattam Waterfalls.  By trekking from Olichuchattam to the upper foothills one can explore different places like Vellarimala, Vavulmala, and Masthakappara.  From the top of Olichuchattam itself one can clearly notice the changes in vegetation and the changes in the landscape because of the altitudinal variations.  The entire waterfall area and adjacent areas are full of wet and moist rocky patches especially in the monsoons and become dry during the summer.  This characteristic habitat enables different plants to survive and adapt in a special way based on the different seasons.

 

Data collection and analysis

The current study was based on extensive exploration and field observations during the period September 2017–February 2018.  In the present study an attempt was made to document and analyse the chasmophytic vegetation of Olichuchattam Waterfall areas of Kozhikode District, Kerala.  The documentation was mainly based on field observations, discussions with local people as well as scrutinizing the literature.  For effective and accurate study, the area was visited and analysed in different climatic conditions in different periods such as rainy season, winter season, and summer season.  The study was mainly based on the rock crevices in nearby areas of the upper regions of the waterfalls (1,400m), near the waterfalls (1,250m), and the lower foothills of the waterfalls (700m) which showed considerable variations in their altitudes ranging 700–1,400 m.

During the field visits, the plant specimens were collected to prepare herbariums.  The collected specimens were identified taxonomically with the help of available floras and literature (Gamble 1915–1936; Sasidharan 2004).  The specimens were processed for the preparation of the herbarium by standard methods.  The voucher specimens are deposited in the Herbaria of PG & Research Department of Botany, St. Joseph’s College, Kozhikode (DEV) for future reference.  Photographs of the study area in different seasons as well as the images of plants were taken.  In addition to these, suitable maps, tables, figures, and images are given in appropriate places.

 

 

RESULTS AND DISCUSSIONS

 

Chasmophytic diversity

Results of the present study reveal 120 species (106 native species and 14 non-native species) belonging to 49 families and 93 genera documented in general (Table 1).  Of these, five species are bryophytes of five families and five genera.  Similarly, in pteridophytes, a total of 10 species belonging to nine families and nine genera are recorded.  Angiosperms are dominant among these groups, which include 105 species that belong to 35 families and 79 genera (Table 2, Figure 2).

The dominant native chasmophytic plant families of the study area are analysed.  The dominant native families are as follows, Poaceae with 15 species followed by Balsaminaceae with seven species, Asteraceae and Commelinaceae with six species each, Malvaceae and Melastomataceae with five species each, and Scrophulariaceae represented by three species (Figure 3).

Similarly, the analysis of the dominant native genera reveals that the genus Impatiens dominates with seven species followed by Blumea, Cyanotis, Eriocaulon, and Arundinella each with three species, respectively (Figure 4).

The analysis of the overall plant habits/growth form reveals that herbs are the dominant with 100 species, followed by 16 species of shrubs and four species of climbers.

 

Distribution pattern of chasmophytic plants

The diversity and distribution of the recorded 120 chasmophytic plants  in the study area reveals that there are only about 25 species which are commonly distributed.  Fifty-eight species are uncommon or sporadically distributed and 37 of them are very rarely occurring in the study area.  The high number of uncommon and rare plants in the study area indicates that they need very specific ecological conditions.

It was observed the distribution of the plants greatly vary with respect to the different seasons.  In the monsoon season, the diversity of water loving chasmophytic plants are seen more. The taxa like Impatiens, Sonerila, Eriocaulon, Utricularia are dominant vegetation cover during this period.  While in the summer period, fewer species survive in the area but grasses and some weedy species are seen thriving well.  Also with the variations in the altitudes, the vegetation changes.  Plants like Pellaea falcata, Bolbitis appendiculata, Impatiens sp., Sonerila sp., Osbeckia sp., Arundinella sp., Pouzolzia wightii, Strobilanthes lanatus, Arundina graminifolia, and Themeda sp. are distributed in high altitude areas (1,200–1,400m).

 

Ornamental chasmophytes

The present study analysed that 47 species of plants have ornamental potential.  Among the 47 species, four of them are pteridophytes and the rest of the 43 species are angiosperms.  Of the 47 species distributed in the area, family Balsaminaceae is dominant with seven species followed by Melastomataceae and Commelinaceae with five species each, Scrophulariaceae and Convolvulaceae with three species each.  Considering the ornamental potential of the plants of documented chasmophytes, 32 species have a good looking habit, seven species have attractive foliage and about 37 species have good looking flowers (Table 3).  The colour of the flowers along with good looking habit of many chasmophytic plants is an aspect of ornamental potentiality, therefore, such taxa has also been identified for possible cultivation in rock gardens or rockeries for ornamental purposes (Binu et al. 2012).

 

Impatiens for rockery/rock gardening

Balsams or Impatiens are often called ‘Jewel Weeds’ or ‘Orchid Balsams’.  They are handsome plants bearing curious and variously coloured flowers.  Southern Indian species of Impatiens have a wealth of new and ornamentally desirable flower colours like red, pink, orange, scarlet, yellow and may have different combinations of these colours.  This beautiful wild flower can be seen on wet perpendicular rocks or old walls in the hills of high elevations.  The balsam thrives best during monsoon months (June–September) and the best collections can only be acquired in the monsoon.  Developing a normal garden for balsams will not be effective because many balsams (especially scapigerous species) cannot survive in normal greenhouses.  So there is a need for a special type of gardening for balsams.  Bhaskar (2012) developed special gardening methods for balsams by providing splash watering, water drippings, and shady conditions which are essential for developing the Impatiens’ microclimate inside greenhouses (Image 6).

 

Invasive chasmophytes

The present study also observed that, there are 14 plant species, which are introduced from various countries as well as different regions of the world and now they are naturalized in chasmophytic habitats of the present study area.  The nativity of these species includes central America, South America, tropical America, and tropical Africa (Sasidharan 2004).  These species are invasive in our country and have established themselves, thereby a threat to other native flora (Table 4).

 

Soil analysis

Soil samples from different regions of the study area (three samples were collected based on altitudinal variations such as lower, middle, higher altitudes) were used for the soil analysis.  Soil samples were analysed with the help of Indian Institute of Spices Research, Kozhikode as per the methods adopted by Jackson (1971).  The parameters analysed are pH value, percentage of organic Carbon, amount of Nitrogen, Phosphorous, and Potassium and the results are presented in Table 5 (Furley 1968).

The soil analysis indicates that the rocky crevices of the lower foothills (700m) is more nutrient rich than the middle and high altitude soils.  This may be due to the washing of the soil and nutrients from the high altitude areas to low altitude areas and the subsequent deposition.  The soil samples of rock crevices are rich in organic carbon and nitrogen due to the weathering of rocks and the deposition of them into the crevices.  The present study also highlights that the growth pattern of chasmophytes in the rock crevices mainly depends on the amount of essential elements in the soil of such micro habitats.

 

Threats to the chasmophytic habitats

Generally, habitat loss is due to the anthropogenic activities.  It was noticed that compared to anthropogenic activities, the present study area was also affected by over grazing as well as unsustainable utilization of natural resources by natives.  It may enhance the depth of threat to the study especially during peak monsoon period by land slides and flooding of rivers.  Invasive species are the biggest threat to many native chasmophytes in the study area.  Tourists trekking the Vellarimala cause destruction to the existing ecosystem to some extent.  There are also many study reports showing that the plants which were distributed earlier in the foothills of Olichuchattam area are disappearing due to the frequent land slides during the monsoon (Manudev et al. 2012).

 

 

CONCLUSION

 

Chasmophytes to some extent determine the vegetation of the valley.  The rocky cliffs and crevices represent a good indicator of rich biodiversity within small areas.  The chasmophytic vegetation hasn’t gained much attention because of the lack of research carried out in this field and the lack of knowledge about this particular vegetation.

 

 

Table 1. Total plant checklist of the study area.

 

Botanical name

Family

Native/ Non-native

Bryophytes

1

Bryum argenteum Hedw.

Bryaceae

Native

2

Campylopus flexuosus (Hedw.) Brid.

Dicranaceae

Native

3

Cyathodium cavernarum Kunze

Targioniaceae

Native

4

Pogonatum aloides (Hedw.) P. Beauv.

Polytrichaceae

Native

5

Riccia crystallina L.

Ricciaceae

Native

Pteridophytes

1

Adiantum raddianum C. Presl

Adiantaceae

Native

2

Bolbitis appendiculata (Willd.) K. Iwats.

Dryopteridaceae

Native

3

Drynaria quercifolia (L) J. Sm.

Drynariaceae

Native

4

Lepisorus nudus (Hook.) Ching

Polypodiaceae

Native

5

Lygodium flexuosum (L.) Sw.

Lygodiaceae

Native

6

Parahemionitis cordata (Roxb. ex Hook. & Grev.) Fras.

Hemionitidaceae

Native

7

Pellaea falcata (R.Br.) Fee

Pteridaceae

Native

8

Pteridium aquilinum (L.) Kuhn.

Dennstaedtiaceae

Native

9

Selaginella involvens (Sw.) Spring

Selaginellaceae

Native

10

Selaginella tenera (Hook. & Grev.) Spring

Selaginellaceae

Native

Angiosperms

1

Abelmoschus angulosus Wall. ex Wight & Arn.

Malvaceae

Native

2

Aeschynomene americana L.

Fabaceae

Non-native

3

Apluda mutica L.

Poaceae

Native

4

Arundina graminifolia (D. Don) Hochr.

Orchidaceae

Native

5

Arundinella leptochloa (Nees ex Steud.) Hook. F.

Poaceae

Native

6

Arundinella metziiHochst. ex Miq.

Poaceae

Native

7

Arundinella pumila (Hochst. ex A. Rich.) Steud.

Poaceae

Native

8

Barleria courtallica Nees

Acanthaceae

Native

9

Blumea barbata DC.

Asteraceae

Native

10

Blumea belangeriana DC.

Asteraceae

Native

11

Blumea membranacea Wall. ex DC.

Asteraceae

Native

12

Bulbophyllum sterile (Lam.) Suresh

Orchidaceae

Native

13

Burmannia coelestis D. Don

Burmanniaceae

Native

14

Canscora diffusa (Vahl) R. Br. ex Roem. & Schult.

Gentianaceae

Native

15

Canscora perfoliata Lam.

Gentianaceae

Native

16

Christisonia tubulosa (Wight) Benth. ex Hook. f.

Orobanchaceae

Native

17

Chromolaena odorata (L.) King & Robins.

Asteraceae

Non-native

18

Chrysopogon hackelii (Hook.f.) C.E.C. Fisch

Poaceae

Native

19

Cleome burmannii Wight & Arn.

Capparaceae

Native

20

Cleome viscosa L.

Capparaceae

Native

21

Commelina benghalensis L.

Commelinaceae

Native

22

Commelina clavata Clarke

Commelinaceae

Native

23

Costus speciosus (Koenig) J.E. Smith

Zingiberaceae

Native

24

Crassocephalum crepidioides (Benth.) S. Moore

Asteraceae

Native

25

Cyanotis arachnoidea Clarke

Commelinaceae

Native

26

Cyanotis cristata (L.) D. Don.

Commelinaceae

Native

27

Cyanotis papilionacea (Burm. f.) Schult. f.

Commelinaceae

Native

28

Cymbopogon flexuosus (Nees ex Steud.) Wats.

Poaceae

Native

29

Cyperus tenuispica Steud.

Cyperaceae

Native

30

Drymaria cordata (L.) Willd.

Caryophyllaceae

Native

31

Emilia sonchifolia (L.) DC.

Asteraceae

Native

32

Eriocaulon quinquangulare L.

Eriocaulaceae

Native

33

Eriocaulon rhodaeFyson

Eriocaulaceae

Native

34

Eriocaulon xeranthemum Mart.

Eriocaulaceae

Native

35

Euphorbia vajraveluiBinoj. & Balakr.

Euphorbiaceae

Native

36

Geissaspis cristata Wight & Arn.

Fabaceae

Native

37

Glinus oppositifolius (L.) A. DC.

Aizoaceae

Native

38

Hemidesmus indicus (L.) R. Br.

Apocynaceae

Native

39

Heteropogon contortus (L.) P. Beauv. ex Roem. &Schult.

Poaceae

Native

40

Hibiscus hispidissimus Griff.

Malvaceae

Native

41

Homonoia riparia Lour.

Euphorbiaceae

Native

42

Hyptis suaveolens (L.) Poit.

Lamiaceae

Non-native

43

Impatiens cordata Wight

Balsaminaceae

Native

44

Impatiens diversifolia Wall. ex Wight & Arn

Balsaminaceae

Native

45

Impatiens gardneriana Wight

Balsaminaceae

Native

46

Impatiens herbicola Hook. f.

Balsaminaceae

Native

47

Impatiens modesta Wight

Balsaminaceae

Native

48

Impatiens scapiflora Heyne ex  Roxb.

Balsaminaceae

Native

49

Impatiens viscosa Bedd.

Balsaminaceae

Native

50

Ipomoea deccana Austin

Convolvulaceae

Native

51

Isachne bourneorum C.E.C. Fisch.

Poaceae

Native

52

Isachneglobosa (Thunb.) O. Ktze.

Poaceae

Native

53

Ischaemum dalzelii Stapf ex Bor

Poaceae

Native

54

Isodon lophanthoides (Buch.-Ham. ex D.Don) H.Hara

Lamiaceae

Native

55

Jansenella griffithiana (C. Muell.) Bor

Poaceae

Native

56

Justicia japonica Thunb

Acanthaceae

Native

57

Knoxia sumatrensis (Retz.) DC.

Rubiaceae

Native

58

Lantana camara L.

Verbenaceae

Non-native

59

Leucas ciliata Benth. ex Wall.

Lamiaceae

Native

60

Lindernia ciliata (Colsm.) Pennell

Scrophulariaceae

Native

61

Lindernia crustacea (L.) F.v. Muell.

Scrophulariaceae

Native

62

Melastoma malabathricum L.

Melastomataceae

Native

63

Melochia corchorifolia L.

Sterculiaceae

Native

64

Merremia umbellata (L.) Hall.

Convolvulaceae

Native

65

Microstachys chamaelea (L.) Muell.-Arg.

Euphorbiaceae

Native

66

Mimosa diplotricha C. Wight ex Sauvalle

Mimosaceae

Non-native

67

Mimosa pudica L.

Mimosaceae

Non-native

68

Mitracarpus hirtus (L.) DC.

Rubiaceae

Non-native

69

Mollugo pentaphylla L.

Aizoaceae

Native

70

Murdannia semiteres (Dalz.) Sant.

Commelinaceae

Native

71

Naregamia alata Wight & Arn.

Meliaceae

Native

72

Oldenlandia corymbosa L.

Rubiaceae

Native

73

Osbeckia aspera (L.) Blume

Melastomataceae

Native

74

Osbeckia virgata D. Don ex Wight & Arn.

Melastomataceae

Native

75

Peliosanthes teta Andr. ssp. humilis

Haemodaraceae

Native

76

Pennisetum polystachyon (L.) Schult.

Poaceae

Native

77

Peperomia pellucida (L.) Kunth

Piperaceae

Non-native

78

Pilea microphylla (L.) Liebm.

Urticaceae

Non-native

79

Pogonatherum crinitum (Thunb.) Kunth

Poaceae

Native

80

Pouzolzia wightii Bennett,

Urticaceae

Native

81

Rotala malampuzhensis Nair ex Cook

Lythraceae

Native

82

Rungia pectinata (L.) Nees

Acanthaceae

Native

83

Scoparia dulcis L.

Scrophulariaceae

Non-native

84

Sida alnifolia L.

Malvaceae

Native

85

Smithia gracilis Benth.

Fabaceae

Native

86

Sonerila rheedei Wight & Arn.

Melastomataceae

Native

87

Sonerila versicolor Wight var. axillaris

Melastomataceae

Native

88

Spermacoce latifolia Aubl.

Rubiaceae

Non-native

89

Spilanthes radicans Jacq.

Asteraceae

Non-native

90

Stemodia verticillata (Mill.) Sprague

Scrophulariaceae

Non-native

91

Strobilanthes lanatus Nees

Acanthaceae

Native

92

Themeda sabarimalayana Sreek. & V.J. Nair

Poaceae

Native

93

Themeda triandra Forssk.

Poaceae

Native

94

Torenia bicolor Dalz.

Scrophulariaceae

Native

95

Tridax procumbens L.

Asteraceae

Non-native

96

Triumfetta annua L.

Tiliaceae

Native

97

Triumfetta rhomboidea Jacq.

Tiliaceae

Native

98

Urena lobata L ssp. lobata

Malvaceae

Native

99

Urena lobata L. ssp. sinuata

Malvaceae

Native

100

Utricularia graminifolia Vahl.

Lentibulariaceae

Native

101

Utricularia striatula Smith

Lentibulariaceae

Native

102

Vernonia cinerea (L.) Less.

Asteraceae

Native

103

Xenostegia tridentata (L.) Austin & Staples

Convolvulaceae

Native

104

Xyris indica L.

Xyridaceae

Native

105

Zeuxine longilabris (Lindl.) Benth. ex Hook. f.

Orchidaceae

Native

 

Table 2. Analysis of chasmophytic diversity in the study area.

 

Analysis of plant diversity

Families

Genera

Species

Bryophyta

5

5

5

Pteridophyta

9

9

10

 

Dicotyledons

Polypetalae

12

26

20

56

*29(3)

73

Gamopetalae

11

30

*26(9)

Monochlamydae

3

6

*4(2)

Monocotyledons

9

23

32

Total

49

93

120

*—native species | ()—Non-native species

 

 

Table 3. List of ornamental chasmophytes from the Olichuchattam area of Kozhikode District, Kerala.

 

Botanical name

Family

Ornamental characters

Pteridophytes

1.

Adiantum raddianum C. Presl

Adiantaceae

Good looking habit and attractive foliage.

2.

Bolbitis appendiculata (Willd.) K.Iwats.

Dryopteridaceae

Good looking habit and attractive foliage.

3.

Pellaea falcata (R.Br.)

Pteridaceae

Good looking habit and attractive foliage.

4.

Selaginellainvolvens (Sw.) Spring

Selaginellaceae

Good looking habit and attractive foliage.

Angiosperms

1.

Abelmoschus angulosus Wall. ex Wight & Arn.

Malvaceae

Attractive large pink coloured flowers

2.

Arundina graminifolia (D.Don) Hochr.

Orchidaceae

Good looking pink/purple coloured flowers also have a good looking habit

3.

Barleria courtallica Nees

Acanthaceae

Attractive light blue coloured flowers.

4.

Burmannia coelestis D.Don.

Burmanniaceae

Attractive light pink coloured flowers.

5.

Canscora diffusa (Vahl) R.Br. ex Roem. & Schult.

Gentianaceae

Good looking habit

6.

Canscora perfoliata Lam.

Gentianaceae

Beautiful cream coloured flowers

7.

Christisonia tubulosa (Wight) Benth. ex Hook.f.

Orobanchaceae

Attractive purple-white tinged-yellow coloured flowers

8.

Commelina benghalensis L.

Commelinaceae

Beautiful blue flowers with good looking habit.

9.

Commelina clavata Clarke

Commelinaceae

Good looking blue coloured flowers with attractive creeping plant habit.

10.

Crassocephalum crepidioides (Benth.) S.Moore

Asteraceae

Good looking yellow-orange coloured flowers and also have attractive pappus hairs.

11.

Cyanotis arachnoidea Clarke

Commelinaceae

Attractive blue coloured flowers and also have attractive habit

12.

Cyanotis papilionacea (Burm.f.) Schult.

Commelinaceae

Attractive blue coloured flowers and nice habit.

13.

Eriocaulon quinquangulare L.

Eriocaulaceae

Attractive plant habit with good looking white headed flowers.

14.

Eriocaulon xeranthemum Mart.

Eriocaulaceae

Attractive plant habit with good looking white headed flowers.

15.

Euphorbia vajravelui Binoj. & Balakr.

Euphorbiaceae

Good looking plant habit.

16.

Geissaspis cristata Wight & Arn.

Fabaceae

Good looking habit, with delicate flowers and persistent fimbriate bracts

17.

Impatiens cordata Wight

Balsaminaceae

A good habit and pink coloured flowers.

18.

Impatiens diversifolia Wall. ex Wight

Balsaminaceae

Attractive pink coloured flowers.

19.

Impatiens gardneriana Wight

Balsaminaceae

Attractive plants with a good habit and pink coloured flowers.

20.

Impatiens herbicola Hook. f.

Balsaminaceae

Small attractive white coloured flowers

21.

Impatiens modesta Wight

Balsaminaceae

Attractive plants with rose coloured flowers.

22.

Impatiens scapiflora Heyne ex Roxb.

Balsaminaceae

Attractive habit and light rose coloured flowers.

23.

Impatiens viscosa Bedd.

Balsaminaceae

Attractive small pink flowers and an attractive habit.

24.

Ipomoea deccana Austin

Convolvulaceae

Good looking purple coloured flowers and attractive habit.

25.

Leucas ciliata Benth. ex Wall.

Lamiaceae

Good looking white flowers.

26.

Lindernia ciliata (Colsm.) Pennell var. ciliata

Scrophulariaceae

Good looking purple flowers with attractive habit.

27.

Lindernia crustacea (L.) Muell.

Scrophulariaceae

Good looking purple flowers.

28.

Melastoma malabathricum L.

Melastomataceae

Attractive large rose coloured flowers.

29.

Merremia umbellata (L.) Hall. f.

Convolvulaceae

Attractive white coloured flowers.

30.

Murdannia semiteres (Dalz.) Sant.

Commelinaceae

Attractive plant habit

31.

Naregamia alata Wight & Arn.

Meliaceae

Good looking white coloured flowers.

32.

Osbeckia aspera (L.) Blume var. aspera

Melastomataceae

Attractive large pink coloured flowers and a good looking habit.

33.

Osbeckia virgata D. Don ex Wight & Arn.

Melastomataceae

Attractive large pink coloured flowers with good looking habit.

34.

Pogonatherum crinitum (Thunb.) Kunth

Poaceae

Attractive plant habit and nice foliage

35.

Rotala malampuzhensis Nair ex Cook

Lythraceae

Attractive plant habit with good looking foliage.

36.

Smithia gracilis Benth.

Fabaceae

Attractive yellow flowers and a good looking habit.

37.

Sonerila rheedei Wight & Arn.

Melastomataceae

Attractive pink coloured flowers

38.

Sonerila versicolor Wight var. axillaris (Wight) Gamble

Melastomataceae

Attractive pink coloured flowers with good looking habit which have leaves with white dots on it.

39.

Torenia bicolor Dalz.

Scrophulariaceae

Attractive dark purple-yellow coloured flowers.

40.

Utricularia graminifolia Vahl.

Lentibulariaceae

Attractive plants with a good habit and blue coloured flowers.

41.

Utricularia striatula Smith

Lentibulariaceae

Attractive plants with pink-yellow coloured flowers.

42.

Xenostegia tridentata (L.) Austin & Staples

Convolvulaceae

Attractive cream to yellow coloured flowers.

43.

Xyris indica L.

Xyridaceae

Good looking plants with beautiful yellow flowers.

 

 

Table 4. List of invasive chasmophytes of study area.

 

Botanical names

Family

Nativity

1.

Aeschynomene americana L.

Fabaceae

Central America

2.

Chromolaena odorata (L.) King

Asteraceae

Central America

3.

Hyptis suaveolens (L.) Poit.

Lamiaceae

Central America

4.

Lantana camara L.

Verbenaceae

Tropical America

5.

Mimosa diplotricha Wight ex Sanv.

Mimosaceae

Tropical America

6.

Mimosa pudica L.

Mimosaceae

South America

7.

Mitracarpus hirtus (L.) DC.

Rubiaceae

Tropical Africa

8.

Peperomia pellucida (L.) Kunth.

Piperaceae

Tropical America

9.

Pilea microphylla (L.) Liebm.

Urticaceae

South America

10.

Scoparia dulcis L.

Scrophulariaceae

Tropical America

11.

Spermacoce latifolia Aubl.

Rubiaceae

Tropical Africa

12.

Spilanthes radicans Jacq.

Asteraceae

Tropical America

13.

Stemodia verticillata Mill.

Scrophulariaceae

Tropical America

14.

Tridax procumbens L.

Asteraceae

Tropical America

 

 

Table 5. Analysis of soil samples from chasmophytic habitats.

Altitudes

pH

Organic carbon (%)

Nitrogen (mg/kg)

Phosphorous (mg/kg)

Potassium (mg/kg)

Lower altitude (700m)

5.00

5.95%

390

5.1

172

Middle altitude (1,250m)

4.71

5.90%

380

4.1

145

Higher altitude (1,400m)

4.52

5.85%

370

3.8

138

 

 

For figures & images - - click here

 

REFERENCES

 

Bashan, Y., C.Y. Li,  V.K.  Lebsky  &  M. Monero (2002). Colonization of chasmophytic plants in arid Baja California, Mexico. Plant Biology 4: 392–402.

Bhaskar, V. (2012). Taxonomic monograph on Impatiens L. (Balsaminaceae) of Western Ghats, South India. The Key Genus for Endemism. Centre for Plant Taxonomic Studies, Bangalore, Karnataka, India, 11–14pp.

Binu, T. &  A. Rajendran (2012). Chasmophytic fern and fern allies of Coimbatore District, Southern Western Ghats, Tamil Nadu, India. Journal of Applied  Biological  Research 11: 1–10.

Binu, T., A. Rajendran & V. Aravindhan (2012). Chasmophytes: the potential plants for Rock gardening, from Velliangiri Hills of Southern Western Ghats of Tamil Nadu, India. Botanical Report 1(1): 14–19.

Danin, A., R.  Gerson, K. Marton & J. Garty (1982). Patterns of limestone and dolomite weathering by lichens and blue – green algae and their paleoclimatic significance. Paleoecology 37: 221–233.

Davis, P.H. (1982). Cliff vegetation in the Eastern Mediterranean. Journal of Ecology 39: 63–93.

Furley, P.A. (1968). The relationships between soil formation and gradient in the Oxford area. Geomorpholgy 12: 25 –42.

Gamble, J.S. &  C.E. CFischer  (1915-1936). The Flora of Presidency of Madras. Part 1- 11 (Part 1-7 by Gamble and 8- 11 by Fischer) Adlard and Sons Ltd., London. (Repr. ed. Vols. 13. 1957).

Jackson, M.L. (1971). Soil Chemical Analysis. Prentice-Hall, New Delhi, India, 498pp.

Manudev, K.M., A. Weber &  S. Nampy (2012). Henckelia pradeepiana, a new species of Gesneriaceae from the southern Western Ghats, India. Rheedea 22(2): 119–123.

Myers, N. (1988 and 1990). Threatened Biotas: hot spots in tropical forests. The Environment 8: 1–20; 10: 243, 256.

Nair, N.C. & P. Daniel (1986). The floristic diversity of the Western Ghats and its conservation: A review. Proceedings of the Indian Academy of Sciences (Animal Science/ Plant Science) Supplement 127–163.

Nayar, M.P. (1996). Hot Spots of Endemic Plants of India, Nepal and Bhutan. Tropical Botanical Garden and Research Institute, Thiruvananthapuram, India, 256pp.

Pascal, J.P., B.R. Ramesh & D. De Franceschi (2004).Wet evergreen forest types of the southern Western Ghats, India. Tropical  Ecology 45(2): 281–292.

Porembski, S. (2000). Biotic diversity of isolated rock outcrops in tropical and temperate regions. Journal of Ecology 146: 177–208.

Roy, D.L., R.W. Miller, C. John &  C. Shickluna (1983). An Introduction to Soil and Plant growth. Prentice-Hall, Englewood Cliffs, NJ, 67–75pp.

Sasidharan, N. (2004). KFRI Handbook, No. 17; Biodiversity documentation for Kerala. Part 6: Flowering plants.

Schimper, A.F. (1898). Plant Geography up on a Physiological Basis. Oxford University Press, England.