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International Journal of
eISSN: 2576-4454

Hydrology

Research Article Volume 2 Issue 6

Fungal flora of tropical riverbanks: indicator for quality running water resources

Saira George, Justin R Nayagam, KI Mani Varghese

Department of Botany, Union Christian College, Aluva (Affiliated to Mahatma Gandhi University, Kottayam) India

Correspondence: Saira George, Department of Botany, Union Christian College, Aluva (Affiliated to Mahatma Gandhi University, Kottayam) India

Received: May 10, 2018 | Published: November 26, 2018

Citation: George S, Nayagam JR, Varghese KIM. Fungal flora of tropical riverbanks: indicator for quality running water resources. Int J Hydro. 2018;2(6):704-707. DOI: 10.15406/ijh.2018.02.00146

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Abstract

River banks of tropics are treasure house of biodiversity. Sacred groves are a part of tradition, which are locations with minimal human interaction in homesteads and hence it is known to be rich in biodiversity from historic time. Taxonomical and ecological studies on different groups of fungi from ten selected sacred groves sites of Central Kerala were studied. Twenty species of fungi were identified from these conserved patches of land. Of these eight were wood rotting fungi and twelve were litter fungi, all indicates their role in bio-geochemical cycle of these regions. Helminthosporium velutinum was a new species record to this region. Torula herbarum found on a new host Ervatamia coronaria. Present studies project that the presence of macro-fungal flora is an indication of limited interaction in the riverbanks as and hence the quality of running water will be considerably good.

Introduction

Sacred Groves are forest patches managed informally as a part of religious and cultural tradition, without ample interference from Government and State Forest Departments.1 Studies on sacred groves recently started with pioneer works done.2 India comprises about 50,000 sacred groves and around 2000 sacred groves had been reported from Kerala.3 Number of groves is reducing drastically now days. From 2011 onwards sacred groves in Kerala are diminishing not due to decline in religious belief but due to religious strategies removing greenery and clear the grove for other purpose.3 Literally, sacred groves represent an in situ conservation method of biodiversity in ancient India. Many species which are rare and extinct in other parts of the country are protected in these groves. They are believed to be the treasure house of medicinal plants, rare and endemic plants, as refugee for relic flora and harbor for seed dispersal.4 Groves are vital parts of life support system and justified as ‘lungs’ of the country by Amruthalingam.5 Four major forest types, namely evergreen, semi-evergreen, moist deciduous and mangrove forests were found in different sacred groves of Kerala by Chandrashekara.6 The general floristic composition and physiognomy of vegetation of the sacred groves are typically like the low level evergreen forest with numerous angiosperms, gymnosperms, bryophytes, pteridophytes, algae and fungi. Floral diversity studies in 577 sacred groves of Kerala by CWRDM7 identified 737 plant species of which 609 were dicotyledons, 122 monocotyledons, 4 pteridophytes and 2 gyymnosperms. Studies in sacred groves of Thrissur district recorded 25 threatened species.8 Studies on herbaceous flora of Iringole kavu reported 68 angeosperms belonged to 28 families and 9 pteridophytes belonged to 5 families.9 Floral survey of Vallikattu kavu in Kozhikode district recorded 245 species of flowering plants belonged to 209 genera and 77 families of which thirty four plants were threatened.10 Survey of lichens in four sacred groves of central Western Ghats recorded 53 species of epiphytic lichen belonging to 30 genera and 15 families.11 Studies on 28 sacred groves of Kerala by Chandrashekara6 identified 670 angiosperm species of which 133 were endemic. The forests of Kerala state is rich in different types of evergreen vegetation and thus provides favorable condition for growth and development of various fungi.12 recorded 1044 taxa of fungi belonging to 414 genera from the state of Kerala. Sankaran et al.,13 recorded 1223 spp. belonging to 464 genera. A documentation made by Maria Florence14 includes a total of 1990 spp. of fungi belonging to 583 genera. The fungal flora of Kerala especially of the Kerala forests remained unexplored except for a few brief surveys carried out by Subramanian & Ramakrishnan,15 Subramanian & Vittal,16 Mani Varghese,17 Hosagouder,18,19 Mohanan,20 etc. Survey of mushrooms flora from Western Ghats were conducted by Thiribhuvanamala et al.21 Marofungal inventory in Western Ghats of Kerala was carried out by Mohanan.22

Perusal of literature clearly indicates that not much work has been carried out on fungal flora of these regions. Ten such sacred groves are selected from Central Kerala.. Therefore diversity studies and ecological aspects are included. The possibility of finding wood rotting and litter fungi is mainly investigated and taxonomical grouping are also incorporated in the study. The present study has its aim to document the fungal flora in the study sites and to establish the possibilities of conservation of fresh water resources and riverbanks to conserve the biodiversity of different life forms.

Materials and methods

Study area includes ten sacred groves of Central Kerala located near river banks. They are Iringole kavu, Chovvazcha kavu, Koozhipilly kavu, Panichayam kavu, Kuzhupilly kavu), Chakarakattu kavu, Palakkattu kavu, Chorian kavu, Vallikattu kavu and Alpara kavu (Table 1) (Figure 1). The largest among the study site Iringole kavu (size of 16 Ha.) to the smallest Panichayam kavu (size of 20 cents), all are well protected by religious view as a part of rituals and hence remain as virgin areas for micro and macro fungi. Fungal fruiting bodies were collected from sample plots of one metre square from ten locations at each study sites during summer seasons from 2007-2010 and 2015-2017. Periodic collection of fungi were made from the above ten sacred groves during summer season from February to April. For field collections, vasculum, lens, knife, scissors, tag were used. Most of the host plants were identified in the field itself.

Sl. No.

(SG)

Site

Area

Coordinates

1

Iringole kavu

SG1

16 ha

10.1091

76.50041

2

Chovvazcha kavu

SG2

0.12 ha

10.1406

76.4587

3

Koozhipilly kavu

SG3

0.10 ha

10.1195

76.4349

4

Panichayam kavu

SG4

0.08 ha

10.1071

76.5634

5

Kuzhupilly kavu

SG5

0.61 ha

10.117

76.4717

6

Chakarakattu kavu

SG6

0.10 ha

10.1279

76.4776

7

Palakattu kavu

SG7

0.20 ha

10.1139

76.4625

8

Chorian kavu

SG8

0.12 ha

10.1058

76.5888

9

Vallikattu kavu

SG9

0.20 ha

10.1323

76.4756

10

Aalpara kavu

SG10

0.40 ha

10.1867

76.4904

Table 1 Location and area of ten selected sacred grooves

Figure 1 Sacred groves (A) Chakarakattu kavu; (B) Panichayam kavu; (C) Kuzhupilly kavu; (D) Palakkattu kavu.

Macro fungal fruit bodies especially of wood rotting fungi were collected as far as possible with the supporting wood. General macro characters of fruit body including colour of different tissues and the type of rot were noted in the field itself. Fruit bodies were wrapped in paper bags and brought to laboratory. Spore prints were taken on micro slides/paper by keeping the fresh fruit body in humid condition. Measurement and detailed observation of fruit body were made in the laboratory and the materials dried in a hot air oven at 70 c. Representative portions of the dried specimens were used for microscopic studies. The rest of the fruit body along with rotten wood were treated with mercuric chloride against mites and moulds and stored with moth balls in paper as voucher specimens. The specimens were brought to the laboratory and infected regions were critically examined using dissection microscope for symptamatology. Tease mounts and scratch mounts were made for microscopic observations. Hand sections were also made. Mounting was done on slide using 5%KOH and lactophenol, as general mounting media. Cotton blue were used for staining. Sections were observed under a research microscope (Olympus trinocular) for studying detailed morphological characters. Measurements of all microscopic structures were taken using micrometer. Drawings were made using a camera lucida (Prism type) attached to the microscope. All the materials collected during this period of investigation were deposited at the Mycological herbarium, Dept of Botany, Union Christian College, Aluva.

Results and discussions

Fungi collected and studied from the present project are classified based on habitat into wood rooting fungi and litter fungi. After critical microscopic observation the materials were assigned to the respective species.

 Wood rotting fungi

Eight species of fungi were collected from living, fallen and decaying woods from these sacred groves (Table 2). All of them belong to the class Basidiomycotina. Among them seven species belonged to order Aphyllophorales and one belonged to Agaricales. Phellinus rimosus and Hexagonia tenuis were perennial species. All other six species were annuals. Pores were not extending to the margin in Polyporus hemicapnodes. Ganoderma lucidum was collected from the base of trunk of living Hydnocarpus pentagyna. But earlier it was reported as basal culm decay of Bambusa bambos, Dendrocalamus strictus, white rot of Artocarpus hirsutus, white spongy rot of Anacardium occidentale etc. from Malappuram, Thrissur, Idukki, and Palakkad districts of Kerala.23‒26 Phellinus rimosus was collected from Artocarpus hirsutus while it was reported from A.heterophyllus by Mohanan.23

Sl. No.

Fungus

Host

Site

1

Coriolopsis caperata (Berk) Murr.

Hopea parviflora Bedd

SG1

Terminalia cattapa Linn.

SG5

2

Ganoderma lucidum (Curt. ex Fr.) Karst.

Hydnocarpus pentagyna Slooten.

SG1

Gymnopilussp. Karsten.

unidentified (dicot)

SG8

decaying wood

3

Hexagonia tenuis ( Hook.)

Calycopteris floribunda

SG1

Fr.

Lam.

4

Lenzites acuta Berk.

Artocarpus heterophyllus

SG9

Lam.

5

Microporus xanthopus (Fr.)

Tectona grandis L.and.

SG1

Kuntze.

Terminalia paniculata

Roth

6

Phellinus rimosus (Berk.)

Ficus benghalensis L.

SG9

Pilat.

Artocarpus hirsutus Lam

 SG1

7

Polyporus hemicapnodes

unidentified branches

SG1

 

Berk. &Br

 

Table 2 Distribution of wood rotting fungi in study area

Litter fungi

Twelve species of fungi were collected from fallen, decaying leaves and twigs (Table 3). All of these fungi belonged to class Duteromycotina and order Moniliales.

Sl. No.

Fungus

Host

 Site

1

Arthrinium sacchari (Speg.) Ellis.

Bambusa bambos (L.) Voss

SG9

2

Beltrania rhombica O. Penzing.

Artocarpus hirsutus Lam.

SG4

Mesua ferrea L.

 SG1

3

Cordella johnstonii Ellis.

unidentified monocot Stem

SG10

4

Dictyoarthrinium sacchari (Stev. In Johnst. & Stev) Damon.

Cocos nucifera L.

SG4

5

Gyrothrix circinata (Berk. &Curt.) Hugues.

Artocarpus hirsutus Lam.

SG3

Cocos nucifera L.

SG2

6

Helminthosporium velutinum Link. ex Ficinus &Schubert

unidentified twigs

SG5

7

Memnoniella levispora Subram

Allamanda cathartica L.

SG2

8

Pithomyces maydicus (Sacc.) Ellis.

Bridelia retusa(L.)A.Juss.

SG6

Bambusa bambos (L.) Voss

SG1

9

Sporidesmium adscendens Berk.

unidentified dead leaves of dicot plant

SG9

10

Sporoschisma mirabile Berk. & Br.

Alstonia scholaris (L.)R.Br.

SG10

11

Tetraploa aristata Berk. &Br.

Bambusa bambos(L.) Voss.

SG9

SG8

12

Torula herbarum f. quaternella Sacc.

Ervatamia coronaria (Jacq.)Stapf.

SG7

 

 

unidentified dicot leaf

SG1

Table 3 Distribution of litter fungi in study area

Setae were present in Beltrania rhombica, Gyrothrix circinata, (branched setae), Sporoschisma mirabile (scattered setae) and Cordella johnstoni (sigle unbranched). Conidia was found in chains in Torula herbarum, Sporoschisma mirabile and Memnoniella levispora. Conidia septate in Torula herbarum (up to 3), Beltrania rhombica, Tetraploa aristata ((longitudinal and transverse), Pithomyces maydicus ((transverse and oblique), Helminthosporium velutinum (6-15 pseudoseptate), Sporoschisma mirabile (up to 3), Sporidesmium adscendens (16-60 pseudoseptate), Dictyoarthrinium sacchari (cruciately septate) and Cordella johnstonii (transverse septa).Septate appendage was observed in Tetraploa aristata. Conidia was formed on groups of phialides in Memnoniella levispora. Conidia was provided with an appendage in Beltrania rhombica. Helminthosporium velutinum was a new report to fungi of Kerala. H. velutinum was reported from monuments of Madanpur, India.27 Another species of this genus, H. dalbergiae was reported from Cherai, Kerala on dead twigs of Tabernae Montana.28 Torula herbarum was found on a new host, Ervatamia coronaria in Kerala. This species was earlier reported from Malayatoor, Kerala, on dead stems of Ichnocarpus frutescens and from dead stems of a dicot plant at Idamalayar, Kerala,28 (Figure 2).

Figure 2 Fruiting body of (A) Ganoderma lucidum (Curt. ex Fr.) Karst; (B) Coriolopsis caperata (Berk) Murr; (C) Gymnopilus sp. Karsten; (D) Microporus xanthopus; (F) Kuntze.

Conclusion

Through the present study the river bank protection is projected to have more importance in protecting the biodiversity especially fungal macro-flora which maybe of various economic interests. Sacred groves from time immemorial were known to be centers of limited human interaction and are treasure house of species diversity. The largest Sacred Grove among the study site Iringole kavu to the smallest Panichayam kavu are well protected by religious view as a part of rituals and hence remain as virgin area for micro and macro fungi. For quality water in the river resources of tropics river bank protection is a must. The present concept may lead to protection of fresh water resources as well as conservation of biodiversity in the future hydro based exploration and utilization.

Acknowledgements

None.

Conflict of interest

The author declares that there are no conflicts of interest.

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