Showing posts with label Conservation. Show all posts
Showing posts with label Conservation. Show all posts

Mosses and More: Exploring the Bryophyte Flora of Kalikasan Park | InformativeBD

Bryophyte Flora of Kalikasan Park, Albay, Philippines

Daile Meek Salvador-Membreve, Erwin N. Baňares, and Jonathan Jaime G. Guerrero, from the institute of Philippines. wrote a Research article about, Mosses and More: Exploring the Bryophyte Flora of Kalikasan Park. Entitled, Bryophyte Flora of Kalikasan Park, Albay, Philippines. This research paper published by the Journal of Biodiversity and Environmental Sciences | JBES. an open access scholarly research journal on Biodiversity. under the affiliation of the International Network For Natural Sciences| INNSpub. an open access multidisciplinary research journal publisher.

Abstract

Bryophytes are nonvascular plants that have ecological and medicinal value. The present study assessed the diversity and ecological status of bryophytes flora in Kalikasan Park, Albay. Sampling plots were established based on the dominant vegetation types in the Park. Collections were made in 20 x 20m in the sampling plots. A total of eight species (8) with five (5) mosses and three (3) species of liverworts were collected in all sampling areas. Microhabitats observed in the study were decayed woods, tree trunks, wet rocks and moist soils. A high index value (2.29) with evenness index of 0.996 was observed in the study area with trees having a much higher index compared to bryophytes found in fern plots. From the species, two (2) species were found to be possibly endangered with one (1) possibly near threatened of IUCN status. Also, three bryophytes found in the area were known to have medicinal value. To date, this is the first record of bryophyte flora in Kalikasan Park.

Submit your article to JBES Journal

Read more : Unraveling the Genetics of Primary Congenital Glaucoma | InformativeBD 

Introduction

Bryophytes are small, photosynthetic, nonvascular and spore-bearing plants. They encompass the terrestrial plants which include mosses, liverworts and hornworts. They occupy various environments from polar to arid conditions but are at their greatest abundance and diversity in tropical rainforests (Valente, Porto and Bastos, 2017). They thrive in trees, rocks, soil, logs and even surfaces of the leaf (Vanderpoorten, Papp and Gradstein, 2010). Bryophytes are known to be indicators of environmental conditions. They are indicator species for air and water quality, heavy metal contamination and climate change (Azuela et al., 2016, Carreon, 2016). Also, they provide habitat and food for arthropods and amphibians (Azuela et al., 2016). Bryophytes are therefore significant for ecological balance. Hence, assessment of bryophytes is thus important.

Kalikasan Park is a man-made forest situated at the back of the Bicol University main campus. It has a total area of ten hectares and the border lies on the Sagumayon River. It is characterized by shrubs, ferns and endemic and non-timber forest trees such as bamboo and rattan. Border areas of the Park are lined with human settlements and agricultural lands.

Infrastructure developments are occurring in the area which might pose a threat to population of bryophytes. Hence, this study aimed to document and determine ecological status of the bryophytes in the Park. This is the first account of bryophytes in the said area.

Reference

Arróniz-Crespo M, Núñez-Olivera E, Martínez-Abaigar J, Becker H, Scher J, Zapp J, Beaucourt N. 2006. Physiological changes and UV protection in the aquatic liverwort Jungermannia exsertifolia subsp. cordifolia along an altitudinal gradient of UV-B radiation. Functional plant biology 33, 1025-1036.

Azuelo A, Manual A, Obemio CD, Oconer E, Gubalane R, Lobredo G. Bryophyte flora of Mt. Matutum protected landscape, South Cotabato, Philippines. 2016. Journal of Biodiversity and Environmental Sciences 9, 1-12.

Azuelo A, Sariana L, Pabualan M. 2010. Diversity and ecological status of bryophytes in Mt. Kitanglad, Bukidnon. Asian Journal of Biodiversity 1, 49-71. Azuelo A, Sariana L, Pabualan M. 2011. Some medicinal bryophytes: their ethnobotanical uses and morphology. Asian Journal of Biodiversity 2, 49-80.

Benítez Á, Prieto M, Aragón G. 2015. Large trees and dense canopies: key factors for maintaining high epiphytic diversity on trunk bases (bryophytes and lichens) in tropical montane forests. Forestry: An International Journal of Forest Research 88, 521-527.

Carreon H, Morales N, Cabras A, Medina MN. 2016. Preliminary list of bryophytes in Tagbaobo, Kaputian, Island Garden City of Samal, Philippines. University of Mindanao International Multidisciplinary Research Journal 1, 152-157.

Gradstein SR, Churchill SP, Salazar Allen N. 2001. Guide to the Bryophytes of Tropical America. The New York Botanical Garden Press, New York.

He X, He K, Hyvönen J. 2016. Will bryophytes survive in a warming world? Perspectives in Plant Ecology, Evolution and Systematics 19, 49-60.

Hespanhol H, Séneca A, Figueira R, Sérgio C. 2011. Microhabitat effects on bryophyte species richness and community distribution on exposed rock outcrops in Portugal. Plant Ecology & Diversity 4, 251-264.

Hipol R, Tolentino D, Fernando E, Dadiz NM. 2007. Life strategies of mosses in Mt. Pulag, Benguet province, Philippines. Philippine Journal of Science 136, 11-18.

Kato-Noguchi H, Seki T. 2010. Allelopathy of the moss Rhynchostegium pallidifolium and 3-hydroxy-β-ionone. Plant signaling & behavior 5, 702-704.

Kumar PREM, Chaudhary BL. 2010. Antibacterial Activity of moss Entodon myurus (Hook) Hamp against some against some pathogenic bacteria. Bioscan 5, 605-608.

Linis VC. 2011. Biogeographical Notes on the Moss Floras of Bicol Penizula in Luzon and Catanduanes Islands, the Philippines. Philippine Journal of Science 142, 119-133.

Valente EDB, Pôrto KC, Bastos CJP. 2017. Habitat heterogeneity and diversity of bryophytes in campos rupestres. Acta Botanica Brasilica 31, 241-249.

Vanderpoorten A, Papp B, Gradstein R. 2010. Sampling of bryophytes. Manual on field recording techniques and protocols for all taxa biodiversity inventories and monitoring 340-354.

Yayintas OT, Sogut O, Konyalioglu S, Yilmaz S, Tepeli B. 2017. Antioxidant activities and chemical composition of different extracts of mosses gathered from Turkey. AgroLife Scientific Journal 6, 205-213.

 Article source : Bryophyte Flora of Kalikasan Park, Albay, Philippines 

Hidden Herps of Lake Mainit: A First Look at Amphibians and Reptiles | InformativeBD

Preliminary report on the amphibians and reptiles of Lake Mainit watershed, Northeastern Mindanao, Philippines

Meconcepcion Ngilangil- Lansang,  Richie P. Lador, and Romell A. Seronay, from the institute of Philippines. wrote a Research article about, Hidden Herps of Lake Mainit: A First Look at Amphibians and Reptiles. entitled, Preliminary report on the amphibians and reptiles of Lake Mainit watershed, Northeastern Mindanao, Philippines. This research paper published by the Journal of Biodiversity and Environmental Sciences | JBES. an open access scholarly research journal on Biodiversity. under the affiliation of the International Network For Natural Sciences| INNSpub. an open access multidisciplinary research journal publisher.

Abstract

Lake Mainit is honored with plentiful assets in both upland and lake ecosystems and is one of the Key Biodiversity Areas (KBA) in the Philippines. A field survey of amphibians and reptiles was conducted in the four municipalities comprising Agusan del Norte portion of Lake Mainit Watershed to determine the species richness, endemicity and conservation status. The methods used were a combination of field observation, reconnaissance survey, pitfall trap method and opportunistic collection. The study found out that 17 species belonging to 13 families, with a total of 69 individuals in the four sampling areas. Polypedates leucomystax recorded the most common species and highest number of individuals followed by Platymantis corrugatus. Highest species diversity index was recorded from Santiago with H’= 1.5. Philippine endemic species were H. pustulatus, P. corrugatus, N. samarensi, M. stejnegeri, H. granducola, P. mindanensis, and S. fasciatus while the two recorded vulnerable species were H. pustulatus and M. Stejnegeri, along these lines, the event of these two species qualifies the area to be protected. In this manner, the low species richness in Lake Mainit watershed could probably go to be archived if the place is completely assessed. Conservation action is still essential to protect and conserve biodiversity in the entire areas.

Submit your article to JBES Journal

Read more  Feeding for Strength: How Natural Diets Boost Mud Crab Growth and Protein | InformativeBD

Introduction

The Philippine Archipelago is one in all the eighteen megadiversity countries that, along is ten times richer in diversity than the Galapagos Island in South American country, with over twenty thousand species of plants and animals endemic to the biological richness of the country (Heaney & Regalado, 1998; Ong et al, 2002; Diesmos & Brown, 2009; Bucol et al, 2011). It houses a spectacular and numerous assemblage of amphibians and reptiles placed at the interface between the faunal zones of the Orient and Australia, has currently jointly recognized as one of the most vital centers of herpetofaunal diversity in South East Asia, creating it so much richer, the amount of endemicity are a lot of higher and therefore the biological process history is much a lot of complicated than are assumed (Diesmos et al, 2002; Ngilangil et al, 2015).

The Mindanao Pleistocene Aggregate Island Complex (Mindanao PAIC) is one giant biogeographically vital sub- province inside the Philippine terra firma (Taylor, 1928; Inger, 1954; Heaney, 1985, 1986; Voris, 2000; Brown & Diesmos, 2009; Sanguila et al, 2016). Mindanao was formed by the accretion of the islandarc associated with the east- central block and also the western continental peninsula block, separated by the Sindangan- Cotabato- Daguma lineament (Yumul et al, 2003; Sanguila et al, 2016). The central part Mindanao has giant isolated mountains that are separated from one another by substantial stretches of low- lying areas that were formed as a result conjointly of collision and geologic process events over the past ten millions years (Hall, 1996, 1998; Yumul et al, 2003, 2009; Sanguila et al, 2016).

This extremely dynamic geologic history suggests the chance of faunal limits to spreading inside early paleoislands, a mechanism which may presumably have contributed to the diversification of the primary amphibian and reptile lineages that inhabited Mindanao (Brown & Alcala, 1970; Brown & Guttman 2002; Evans et al, 2003; Sanguila et al, 2011; 2016; Brown et al, 2013; Barley et al, 2013).

Amphibians and reptiles, cold- full- blooded animals, are regarding one- fourth of all well- known vertebrate species distributed worldwide (Zug et al, 2001; Ali & Bukhari, 2018). They are good biological indicators as a result of they are more sensitive to the environment than other wildlife (Hopkins, 2007; Coritico et al, 2018) and a very important part of healthy scheme as they play a vital role in the food pyramid by maintaining the balance of food cycle thus, they provide an excellent starting point for inventorying and monitoring biodiversity. Moreover, they recycle nutrients between aquatic to terrestrial environments, and removal of those species from any scheme can cause to disturbances in predator- prey dynamics, invertebrate populations, alga communities, leaf litter decompositions, and nutrient cycling, however their population is depleting day by day because of several anthropogenic activities like intensive grazing, forest cutting and burning, mining areas restorations (McLeod & Gates, 1998; Ngilangil et al, 2015) fragmentation, and changes in microclimatic variables through a disturbed gradient within the home ground structure (Ward, 2006; Ngilangil et al, 2015).

Lake Mainit is recognized as the deepest (219.35 meters), fourth biggest (17, 060 ha), one of the cleanest lakes in the Philippines, flanked by mountain ranges at the north, east and west, with a broad aluvial plain at the south and is circumscribed by eight municipalities that comprise the Lake Mainit Watershed (LMDA, 2005; SFM Program, 2009; LMHGC- ESIA, 2013 and Padilla et al, 2015. Subsequently, Lake Mainit is honored with plentiful assets in both upland and lake ecosystems as appeared in researches and studies conducted by various institutions (Gracia, 1981; Demetillo et al, 2015). However, the forest cover of Lake Mainit has been fragmented and degraded into vast open grassland habitats, while some areas are converted into agricultural lands. Remaining forest cover in the watershed is currently threatened by various unregulated anthropogenic activities such as rural development, cryptic small-scale mining, and illegal logging of the remaining tree stands (LMDA-EMP, 2014 and Padilla et al, 2015).

Be that as it may, the information was generated quite a long while prior, which right now needs assessment and validation. Thus, this study aims to determine species distribution, abundance, endemism and conservation status of amphibians and reptiles within the sampling sites of the Lake Mainit watershed area.

Reference

Alcala AC, Brown WC. 1998. Philippine amphibians: An illustrated field guide. Makati: Bookmark Inc. Press 113 pp.

Alcala AC, Bucol AA, Diesmos AC, Brown RM. 2012. Vulnerability of Philippine amphibians to climate change. Philippine Journal of Science 141, 77-87.

Alcala AC. 1986. Guide to Philippine flora and fauna: Amphibians and reptiles. Manila: Natural Resource Management Center, Ministry of Natural Resources and the University of the Philippines 195 pp.

Ali W, Javid A, Hussain A, Bukhari SM. 2018. Diversity and habitat preferences of amphibians and reptiles in Pakistan: A review. Journal of Asia-Pacific Biodiversity 173-187.

Almeria ML, Nuñeza OM. 2013. Diet of seven anuran species (Amphibia: Anura) in Agusan Marsh, Mindanao, Philippines. ABAH Bioflux, 2013, Volume 5, Issue 1.

Balmores MN, Nuñeza OM. 2015. The reptiles of Bega watershed of the province of Agusan del Sur in the Philippines. World Journal of Environmental Biosciences. Volume 4, Issue 2, 50-61.

Barley AJ, White AC. Diesmos and Brown R.M. 2013. The challenge of species delimitation at the extremes: diversification without morphological change in Philippine sun skinks. Evolution 67, 3556-3572. https://doi.org/10.1111/evo.12219.

Barthlott W, Lauer W, Placke A. 1996. Global distribution of species diversity in vascular plants: Towards A World Map of Phytodiversity. Erdkunde 50, 317-327.

Brown RM, Diesmos AC. 2009. Philippines, Biology Gillespie R, Clague D (eds). Encyclopedia of Islands. University of California Press, Berkeley, CA, USA. pp 723-732.

Brown RM, Guttman SI. 2002. Phylogenetic systematics of the Rana Signata complex of Philippine and Bornean stream frogs: Reconsideration of Huxley’s modification of Wallace’s Line at the Oriental- Australian faunal zone interface. Biological Journal Linnean Society 76, 393-461.

Brown RM, Oliveros CH, Siler CD, Fernandez JB, Welton LJ, Buenavente PAC, Diesmos MLL, Diesmos AC. 2012. Amphibians and reptiles of Luzon Island (Philippines), VII: herpetofauna of Ilocos Norte Province, northern Cordillera Mountain Range.

Brown RM, Siler CD, Diesmos AC, Alcala AC. 2009. The Philippine frogs of the genus Leptobrachium (Anura: Megophyridae): Phylogeny- based species delimitation, taxonomic revision, and description of the three new species. Herpetological Monographs 23, 1-44. DOI: 10.1655/09-037.1.

Brown RM, Siler CD, Oliveros CH, Welton LJ, Rock AS wab J, Weerd MV, Beijnen JV, Jose E, Rodriguez D, Jose E, Diesmos AC. 2013. The Amphibians and Reptiles of Luzon Island, Philippines VIII: the herpetofauna of Cagayan and Isabela Provinces, northern Sierra Madre Mountain Range.

Brown WC, Alcala A. 1970. The zoogeography of the herpetofauna of the Philippine Islands, a fringing archipelago. Proceedings of the California Academy of Sciences (4)38 (6), 105130.

Brown WC, Alcala AC. 1978. Philippine Lizards of the family Gekkonidae. Siliman University. Nat Sci Monogr Ser 1, Dumaguete City, Philippines 131.

Brown WC, Alcala AC. 1980. Philippine Lizards of the family Scincidae. Siliman University. Nat Sci Monogr Ser 1, Dumaguete City, Philippines 263.

Bucol AA, Alcala AC, Averia1 LT, Alcala EL, Alcala MLR. 2011. Checklist of the Herpetofauna of Siquijor Island, Philippines. Philipp. Scient 48, 100-122.

Coritico FP, Sinamban EB, Mohaganm AB, Amoroso VB. 2018. Preliminary Report on the Anurans of Mt. Pantaron Range, Bukidnon, Central Mindanao, the Philippines. Journal of Nature Studies 17(1), 9-23.

David P, Pauwels OSG, Lays PFG, Lenglet GL. 2006. On a collection of reptiles from Southern Mindanao Island, the Philippines. Bulletin De L ‘Institut Royal Des Sciences Naturelles De Belgique 76,201-227, 2006.

Demetillo MT, Lador RP, Seronay, RA. 2015. Floral Assessment in Lake Mainit Watershed, Caraga Region, Mindanao Philippines. Annals of Studies in Science and Humanities Volume 1 Number 2 (2015), 12-28.

Diesmos AC, Brown R, Gee G. 2003. Preliminary Report on the amphibians and Reptiles of Balbalasang-Balbalan National Park in Luzon Island, Philippines. Sylvatrop The Technical Journal of Philippine Ecosystems and Natural Resources 131(2), 63-80.

Diesmos AC, Brown RM, Alcala AC, Sison RV, Afuang LE, Gee GVA. 2002. Philippine amphibians and reptiles. In Ong P. S., Afuang L. E., and Rosell-Ambal R. G. (Eds.) Philippine Biodiversity Conservation Priorities: a Second Iteration of the National Biodiversity Strategy and Action Plan. Department of the Environment and Natural Resources— Protected Areas and Wildlife Bureau, Conservation International Philippines, Biodiversity Conservation Program—University of the Philippines Center for Integrative and Developmental Studies, and Foundation for the Philippine Environment. Quezon City, Philippines 26-44.

Diesmos AC, Brown RM. 2009. Diversity, biogeography, and conservation of Philippine amphibians; pp. 26–49, in: I. Das, A. Haas & A. Alek Tuen (Eds.). Biology and conservation of tropical Asian amphibians. Proceedings of the Conference on Biology of the Amphibians in the Sunda Region, South-east Asia.

Diesmos AC, Watters JL, Huron NA, Davis DR, Alcala AC, Crombie RI, Afuang LE, Gee-Das G, Sison RV, Sanguila MB, Penrod ML, Labonte MJ, Davey CS, Leone EA, Diesmos ML, Sy EY, Welton LJ, Brown RM, Siler CD. 2015. Amphibians of the Philippines, part I: checklist of the species. Proceedings of the California Academy of Sciences 62, 451-531.

Evans BJ, Brown RM, McGuire JA, Supriatna J, Andayani N, Diesmos AC, Iskandar D, Melnick DJ, Cannatella DC. 2003. Phylogenetics of fanged frogs: testing biogeographical hypotheses at the interface of the Asian and Australian faunal zones. Systematic Biology 52, 794-819.

Gotame B. 2008. Economics of Biodiversity Conservation in Nepal. The Initiation, 2(1), 55-61.

Gracia DM. 1981. Report on the hydrobiological survey and inventory of aquatic resources of Lake Mainit, Mindanao Island. Terminal report. Manila, BFAR Fish Propagation Division.

Hall R. 1996. Reconstructing Cenozoic SE Asia. In: Hall R, Blundell D (Eds) Tectonic evolution of Southeast Asia. Geological Society, London 153-184. DOI: 10.1144/gsl. sp.1996.106.01.11

Hall R. 1998. The plate tectonics of Cenozoic SE Asia and the distribution of land and sea. In Hall R., Holloway J. D. (Eds.), Biogeography and Geological Evolution of Southeast Asia. Leiden: Brackhuys 99-132.

Heaney LR, Regalado JC. 1998. Vanishing treasures of the Philippine rain forest. The Field Museum, Chicago, USA.

Heaney LR. 1985. Zoogeographic evidence for middle and late Pleistocene land bridges to the Philippine Islands. Modern Quaternary Research in Southeast Asia 9, 127-144.

Heaney LR. 1986. Biogeography of mammals in SE Asia: estimates of rates of colonization, extinction and speciation. Biological Journal of the Linnean Society 28, 127-165. https://doi. org/10.1111/j.1095-8312. 1986.tb01752.x

Hopkins WA. 2007. Amphibians as models for studying environmental change. ILAR Journal   48(3), 270-277.

Inger RF. 1954. Systematics and zoogeography of Philippine Amphibia. Fieldiana 33, 181-531. doi: 10.5962/bhl.title.5571

IUCN. 2016. IUCN Red List of Threatened Species. Version 1016-1. http://www.iucnredlist.org.

Magurran AE. 1988. Ecological diversity and its measurement. Princeton University Press, Princeton N.J.

McLeod RF, Gates JE. 1998. Response of Herpetofaunal Communities to Forest Cutting and Burning at Chesapeake Farms, Maryland. The American Midland Naturalist Vol. 139, No. 1 pp. 164-177.

Ngilangil MM, Boyles LZ, Sularte RP. 2014. Abundance, Distribution and Conservation Status of Reptiles in Agusan Marsh, Bunawan, Agusan del Sur, Philippines. International Journal of Advances in Chemical Engineering, & Biological Sciences 1(2), 2349-1507.

Nuñeza OM, Ates FB, Alicante AA. 2010. Distribution of endemic and threatened herpetofauna in Mt. Malindang, Mindanao, Philippines. Biodiversity Conservation 19, 503-518. DOI: 10.1007/ s10531-009-9742-z

Nuneza OM, Fabricante KMB, Alicante AA, Sucaldito MO, Ponce AG. 2012. The Herpetofauna of Mounts Sambilikan, Ararat and Berseba of the Diwata Range, Agusan del Sur, Philippines.

Ong PS, Afuang LE, Rosell-Ambal RG. 2002. Philippine Biodiversity Conservation Priorities: A Second Iteration of the National Biodiversity Strategy and Action Plan. DENR–PAWB, Conservation International Philippines, Biodiversity Conservation Program UP Center for Integrative and Development Studies and Foundation for the Philippine Environment, Quezon City, Philippines.

Padilla RFQ, Crisologo ES, Romarate IIRA, Vedra SA. 2015. Analysis of vegetation degradation using GIS and remote sensing at Lake Mainit watershed, Mindanao, Philippines. Advances in Environmental Sciences- International Journal of the Bioflux Society Volume 7, Issue 3.

Sanguila MB, Cobb KA, Siler CD, Diesmos AC, Alcala AC, Brown RM. 2016. The amphibians and reptiles of Mindanao Island, southern Philippines, II: the herpetofauna of northeast Mindanao and adjacent islands. ZooKeys 624, 1-132. https://doi.org/10.3897 /zookeys.624.9814.

Sanguila MB, Siler CD, Diesmos AC, Nuñeza O, Brown RM. 2011. Phylogeography, geographic structure, genetic variation, and potential species boundaries in Philippine slender toads. Molecular Phylogenetics and Evolution 61, 333-350. DOI: 10.1016/j.ympev.2011.06.019.

Siler CD, Lira-Noriega A, Brown RM. 2014. Conservation genetics of Australasian Sailfin Lizards: flagship species threatened by coastal development and insufficient protected area coverage. Biological Conservation 169, 100-108.

Smith BE. 1993. Notes on a collection of squamate reptiles from eastern Mindanao, Philippine Islands part 1: Lacertilia. Asiatic Herpetological Research 5, 85-95.

Sustainable Fisheries Management (SMF) Program for Lake Mainit. 2009. Phase II Comprehensive Resource Assessment. Prepared by MSU Naawan Foundation for Science and Technology Development (MSUNFSTDII). MSU Naawan Campus.

Taylor EH. 1928. Amphibians, lizards, and snakes of the Philippines. In Dickerson R. (Ed.), Distribution of Life in the Philippines. Manila: Bureau of Science, Monogr 21, 322 pp.

Voris HK. 2000. Maps of Pleistocene sea levels in Southeast Asia: shorelines, river systems, time durations. Journal of Biogeography 27, 1153-1167. DOI: 10.1046/j.1365-2699.2000.00489.x.

Ward AC. 2012. Composition, distribution and conservation of the herpetofauna of Santa Barbara mountain, Honduras. Graduate Student Theses, Dissertations, & Professional Papers 231.

Yumul GP, Dimalanta CB, Queaño K, Marquez E. 2009. Philippines, geology. In: Gillespie Rand, Clague D (Eds) Encyclopedia of Islands. University of California Press, Berkeley 732-738.

Yumul GP, Dimalanta CB, Tamayo RA, Maury RC. 2003. Collision, subduction and accretion events in the Philippines: A synthesis. Island Arc 12, 77-91. DOI: 10.1046/j.14401738.2003.00382.x

Yusuf AA, Francisco HA. 2009. Climate Change Vulnerability Mapping for Southeast Asia. Singapore: Economy & Environment Program for South East Asia 32p.

Zug GR, Vitt LJ, Caldwell JP. 2001. Herpetology: An Introductory biology of amphibians and reptiles. USA: Academic Press pp.1-527. 

Article source Preliminary report on the amphibians and reptiles of Lake Mainit watershed, Northeastern Mindanao,Philippines  

Winged Residents of the Mangroves: Understanding Avifauna Diversity in Misamis Oriental | InformativeBD

Factors affecting avifauna diversity in selected mangrove areas of Misamis Oriental, Philippines: Basis for conservation and management

Joly Bee A. Olila, and Richel E. Relox, from the different institute of Philippines. wrote a Reseach Article about, Woody Allies: How Chagga Home Gardens Sustain Insect Pollinators in Northern Tanzania. Entitled, Factors affecting avifauna diversity in selected mangrove areas of Misamis Oriental, Philippines: Basis for conservation and management. This research paper published by the Journal of Biodiversity and Environmental Sciences | JBES. an open access scholarly research journal on Biodiversity. under the affiliation of the International Network For Natural Sciences| INNSpub. an open access multidisciplinary research journal publisher. 

Abstract

Ecological and anthropogenic factors may influence the distribution and diversity of birds. This study assessed the avifauna and mangrove species composition, abundance, and diversity as well as the socio-economic and institutional conditions in three coastal ecosystems of Molugan, El Salvador City; Baybay, Alubijid and Tubajon, Laguindingan, Misamis Oriental. Point count and mist-netting methods were used to survey birds, quadrat method to survey mangroves, household survey to 212 respondents and Geographic Information System (GIS) in mapping birds, mangroves and human activities. Results showed a total of nine (9) Orders, 19 Families, 22 species and 1,168 individuals were documented in three selected areas. Baybay had the highest diversity index (2.46), followed by Molugan (1.96) and Tubajon got the lowest (1.70). As for the mangroves, five (5) species were recorded namely: Rhizophora mucronata, Sonneratia alba, Avicennia alba, Avicennia rumphiana and Rhizophora apiculata. However, continuing threats such as growing human population, land-use changes and weak management in the coastal ecosystems led to its unsustainability. Thus, the diversity of birds is highly dependent on the mangrove species and zonation and human activities in the coastal areas. Hence, regular monitoring of programs and policies by stakeholders to ensure sustainability and conservation of birds and mangroves species is recommended.

Submit your article to JBES Journal

Read moreWoody Allies: How Chagga Home Gardens Sustain Insect Pollinators in Northern Tanzania IInformativeBD

Introduction

The Philippine archipelago which is composed of 7,100 distinct islands (Ambal et al., 2012) is recognized as one of the 17 mega diverse countries which contain two-thirds of the earth’s biodiversity and about 70-80% of the world’s flora and fauna species. Avifauna refers to a group of birds that are found almost everywhere on the planet which shows great diversity by their habitat and geographical conditions (Tandan et al., 2015). Birds are valuable indicators of global patterns in biodiversity conservation (Mallari et al., 2011). Avifauna provides several ecological functions such as pest control, pollination, seed dispersal, and plant reproduction in thousands of economically and culturally important plant species through its consumption of several terrestrial, marine, and aerial resources (Whelan et al., 2015). The bird population is a sign of environmental changes as they respond fast to threats and changing environmental conditions (Mallari et al., 2011). However, few are aware of the importance of birds and are greatly affected by human development which leads to the loss of its species. Mangroves belong to a higher group of plants which may exist as trees, shrub, palm, herb, or fern (Primavera et al., 2004). It is a habitat of different avifauna species where they can hatch their eggs (Duke et al., 2007). Mangrove is the one that lessens the impact of tsunamis, hurricanes, cyclonic storms on human lives, properties and helps to prevents flooding and it is the one who catches the waste generated by humans (Danielsen et al., 2005). The mangrove habitat loss caused by deforestation, urbanization, salt production, conversion into paddy fields and aquaculture ponds, over-harvesting of timber and fuel wood, pollution, dumping of domestic sewage and crude oil exploration (Giri, 2011), and degradation has posed major threats to a wide array of fauna bringing them among the ranks of endangered and extinct species (Sandilyan et al., 2010). Thus, there is an urgent demand to examine the avifauna diversity inhabiting mangrove habitats to know the impact of disturbance for future conservation and management.

Reference

Abino AC, Castillo JAA, Lee YJ. 2014. Assessment of Species Diversity, Biomass and Carbon Sequestration Potential of a Natural Mangrove stand in Samar, the Philippines. Forest Science and Technology 10, 1.

Alemayehu F, Onwonga R, Kinyanjui M, Wasonga JO. 2014. Assessment of Mangrove Covers Change and Biomass in Mida Creek, Kenya. Open Journal of Forestry 4, 398-413.

Alviola GL, Del Rosario BI, Otadoy JB, Ibanez JC. 2010. Birds of Malagos Watershed, Southeastern Philippines. Asian Journal of Biodiversity 1(1).

Alviola GL, Mohagan A. 2017. Assessment of Bird Species in Central Mindanao University, Bukidnon, Philippines. Journal of Biology and Life Science Vol 8, No. 2. 2157-6076.

Ambal RGR, Duya MV, Cruz MA, Coroza OG, Vergara SG, de Silva N, Molinyawe N, Tabaranza B. 2012. Key Biodiversity Areas in the Philippines: Priorities for Conservation. Journal of Threatened Taxa 4(8), 2788-2796.

Ascaño II CP, Albutra QB, Ansigbat VV, Mugot DA, Demayo CG. 2016. Avifauna Assessment in and around the Hydraulic Mining Area of Brgy. Tumpagon, Cagayan de Oro City, Philippines. Journal of Scientific Research and Development 3(4), 83-90.

Branch FM, May J, Roberts B, Russell E, Clark BM. 2002. “Case studies on the socio-economic characteristics and lifestyles of subsistence and informal fishers in South Africa,” South African Journal of Marine Science 24, 439-462.

Cailing CAG, Caban JLS, Cultura, RKM, Relox RE. 2018. Relationship of Avifauna and Mangroves in Laguindingan, Misamis Oriental, Philippines. Journal of Biodiversity and Environmental Sciences 13(1), 216-222.

Calimpong DMT, Nuñeza OM. 2015. Avifaunal diversity of Bega Watershed, Prosperidad, Agusan del Sur, Philippines. Journal of Biodiversity and Environmental Sciences 6(4), 385-400.

Danielsen F, Sørensen MK, Olwig MF, Selvam V, Parish F, Burgess ND, Hiraishi T, Karunagaran VM, Rasmussen MS, Hansen LB, Quarto A, Suryadiputra N. 2005.      The Asian Tsunami: A Protective Role for Coastal Vegetation. Science 310(5748), 643.

Duke NC, Meynecke JO, Dittmann S, Ellison AM, Anger K, Berger U, Cannicci S, Diele K, Ewel KC, Field CD, Koedam N, Lee SY, Marchand C, Nordhaus I, Dahdouh-Guebas F. 2007. A World without Mangroves. Science 317, 41-42.

Ellison AM. 2015. Managing mangroves with benthic biodiversity in mind: moving beyond roving banditry. Journal Sea Research 59, 215.

Giliba RA, Boon EK, Kayombo CJ, Chirenje CI, Musamba EB. 2011. “The influence of socio-economic factors on deforestation: a case study of the bereku forest reserve in Tanzania,” Journal of Biodiversity, vol 2, pp. 31-39.

Giri C. 2011. Status and Distribution of Mangrove Forests of the World using Earth Observation Satellite Data. Global Ecology Biogeography 20, 154-159.

Harrison T. 1976. The food of Aerodramus mearnsi (Aves, Apodidae) at Niah Great Cave, in Borneo. F. Bombay Nat. Hist. Soc 71, 376-393.

Honda K, Nakamura Y, Nakaoka M, Uy WH, Fortes MD. 2013. Habitat Use by Fishes in Coral Reefs, Seagrass Beds and Mangrove Habitats in the Philippines. PLoS ONE 8(8).

Jin H, Wang Z, Ran S, Yun C. 2003. “Study on coastal resource evaluation theories and methods,” in Proceedings of the International Conference on Estuaries and Coasts pp. 9-11.

Kennedy RS, Gonzales PC, Dickinson EC, Miranda HC, Fisher TH. 2000. A Guide to the Birds of the Philippines. Oxford University Press Inc., New York.

Malavashi R, Battisti C, Carpaneto GM. 2009. Seasonal Bird assemblages in a Mediterranean patchy wetland: corroborating the intermediate disturbance hypothesis. Polish Journal of Ecology 57(1), 171-179.

Mallari NA, Collar N, Lee DC,mcGowan PJK, Wilkinson R, Marsden SJ. 2011. Population Densities of Understorey Birds Across a Habitat Gradient in Palawan, Philippines: Implications for Conservation. Oryx 45, 234-242.

Mariano HG, Dagoc FLS, Espra AS, Ruben F, Amparado RF. 2019. Mangrove diversity, taxonomic classification, and morphological characteristics of natural and reforested mangrove forests in selected municipalities of Zamboanga Del Sur, Mindanao Island, Philippines. Journal of Biodiversity and Environmental Sciences (JBES), Vol 15, No. 4, p. 86-99.

Mengesha G, Bekele A. 2008. Diversity and relative abundance of birds of Alatish National Park International Journal of Ecology and Environmental Science 34, 215-222.

Mohagan AB, Nuñeza OM, Gracia AG, Selpa ECT, Escarlos JA, Baguhin LJB, Coritico FP, Amoroso VB. 2015. Species Richness of Avifauna in Four Long Term Ecological Research Sites in Mindanao, Philippines. Journal of Applied Environmental and Biological Sciences.

Mtwana L. 2012. Nordlund, People and the Intertidal: Human Induced Changes, Biodiversity Loss, Livelihood Implications and Management in the Western Indian Ocean.

Nordlund LM, Unsworth RKF, Gullström M, Cullen-Unsworth LC. 2018. “Global significance of seagrass fishery activity,” Fish and Fisheries, vol     19, no. 3, pp. 399-412.

Pototan BL, Capin NC, Tinoy MRM, Novero AU. 2017. Diversity of Mangrove Species in three Municipalities of Davao del Norte, Philippines. Aquaculture, Aquarium, Conservation and Legislation – Bioflux Society 10(6).

Primavera JH, Sadaba RS, Lebata NJHL, Altamirano JP. 2004. Handbook of Mangroves in the Philippines–Panay. SEAFDEC Aquaculture Department, Iloilo, Philippines 106pp.

Relox RE, Leano EP, Camino FA. 2011. Avifaunal Assemblage in Mt. Hamiguitan, Davao Oriental, Mindanao Island, Philippines. Journal of Environmental Science and Management 14(1), 1-11.

Sandilyan S, Thiyagesan K, Nagarajan RM. 2010. Decline in species-richness of waterbirds in the Pichavaram mangrove wetlands, southern India. Wader Study Group Bull 117, 91-98.

Sarmin NS, Mohd Hasmadi I, Pakhriazad HZ, Khairil WA, Monjurur R, Khalid I. 2018. Community Perception on Mangrove Change Issue in Southwest Johor, Malaysia. International Journal of Engineering & Technology 7(37), 171-173.

Shackleton SC, Delang O, Angelsen A. 2011. “From subsistence to safety      nets and cash income: exploring the diverse values of non-timber forest products for livelihoods and poverty alleviation,”in Non-Timber Forest Products in the Global Context pp. 55-81, Springer.

Tagupa VMF, Besoro ET, Bacas TDL, Labiao RJG, Sinco AL, Raagas EL. 2017. Avifaunal Assemblage in Barangay Lumbia, Cagayan de Oro City, Philippines. Journal of Biodiversity and Environmental Sciences 11(5), 169-178.

Tandan HN, Maheshwari R, Tandan S. 2015. Avifaunal diversity of Pt. Ravishankar Shukla University Campus, Raipur (Chhattisgarh). IOSR Journal of Environmental Science, Toxicology and Food Technology 1(6), 41-44.

Welsh DA.1987. The influence of forest harvesting on mixed coniferous-deciduous boreal bird communities in Ontario 8, 247-252.

Whelan CJ, Sekercioglu CH, Wenny DG. 2015. Why Bird Matter from Economic Ornithology to Ecosystem Services? Journal Ornithology 156, 227-238.

Article sourceFactors affecting avifauna diversity in selected mangrove areas of Misamis Oriental, Philippines:Basis for conservation and management

 


Population Size and Conservation Strategies for Rose-Ringed Parakeet in Maroua, Northern Cameroon | InformativeBD

Population size and conservation management of the rose-ringed parakeet (Alexandrinus krameri) in the town of Maroua, far north Cameroon

Ghislain Noé Kougoum Piebeng, from the institute of  Cameroon,  Madi Namissa , from the institute of  Cameroon. Simon Awafor Tamungang , from the institute of  Cameroon. Daksala Wansang , from the institute of  Cameroon.  Leonce Syntcha Djakam, from the institute of  Cameroon . Sandra Ateufack Nguekeng, from the institute of  Cameroon and Alexis Teguia, from the institute of  Cameroon. wrote a research article about, Population Size and Conservation Strategies for Rose-Ringed Parakeet in Maroua, Northern Cameroon. entitled, Population size and conservation management of the rose-ringed parakeet (Alexandrinus krameri) in the town of Maroua, far north Cameroon. This research paper published by the Journal of Biodiversity and Environmental Sciences (JBES).  an open access scholarly research journal on Biodiversity. under the affiliation of the International Network For Natural Sciences | INNSpub. an open access multidisciplinary research journal publisher. 

Abstract

The present study was carried out in the town of Maroua, Far North Region of Cameroon with the main objective of contributing to the knowledge of the population status of the Rose-ringed Parakeet (RRP) with a view to its sustainable management. The Rose-ringed Parakeet (RRP) inventory was carried out using the linear strip transect method. The counts were made from 27 July to 20 September 2023 for the rainy season and from 15 November 2023 to 2 February 2024, all between 6 a.m.-9:30 a.m. for the morning and 4 p.m.-6 p.m. for the evening on all sites. The information collected in the field was processed and analysed using Distance 6.0, PAST 4.03 and QGIS.3.22 software. It appears from this analysis that the population of RRP is estimated at 47,391 individuals in the study site with an average density of 20.6 individuals per hectare. In the rainy season, the surface density was estimated at 12,488 individuals/ha for a total of 28,723 individuals while in the dry season, the density was 7.1815 individuals/ha for a total of 16,517 individuals. Depending on the type of habitat, the abundance of parakeets was higher in mixed zones composed of housing and plantations compared to other habitats. RRP are found everywhere in the territory of the city of Maroua. Modelling the spatial distribution using the IDW interpolation method using QGIS software shows that RRP in general and in the rainy season are more abundant in the Maroua 1 subdivision, and this distribution was dependent on the availability of food resources. Les principales activités humaines rencontrés sont le pâturage et l’exploitation forestière. The main human activities encountered were pasture and logging. Although RRPs are still encountered in large numbers in Maroua, conservation should be done as a priority in the districts of Maroua 1 and Maroua 3.

Submit your article to JBES Journal

Read moreInnovative Approaches to Atherosclerosis Treatment: Nanomedicine and Herbal Remedies | InformativeBD

Introduction

Birds represent the animal group most used for environmental monitoring, ahead of large mammals (Ricard et al., 2017). They play a role in crop protection by controlling populations of harmful insects. They enable the development of tourist activities through their various forms (Kouzi, 2012). Birds are a source not only of aesthetic pleasure, sound and color to our existence, but also a source of economic growth, providing income and motivation for conservation through ecotourism (Jaquemet, 2010). They also provide a wide variety of ecosystem services. Rose-ringed parakeets (RRP), for their part, are involved in the pollination of plants and can disperse seeds over long distances through their excrement (Blanco et al., 2018). The potentially ubiquitous ecological role of the parakeet may contribute to the resilience of ecosystems against overgrazing and forest degradation, particularly through their dependence on declining basal tree species (Ellison et al., 2005). 

The RRP, despite its ecological and socioeconomic importance, is one of the most successful invasive birds in the world (Menchetti and Mori, 2014; Le Gros et al., 2016), with exotic populations established in more than 35 countries (Menchetti et al., 2016). The rose-ringed parakeet often occurs around human habitation (Grandi et al. 2018; Mentil et al. 2018). It is a social species and is native to parts of eastern and southern Asia and from eastern to central Africa (Parr and Juniper, 2010). Humans have been responsible for translocating this species across the globe as part of the pet trade, and many are purchased for companionship (Menchetti et al., 2016; Vall-llosera et al., 2017). The RRP with its shrill cry is a granivore-frugivore which exploits both local and exotic species (buds, fruits, seeds). It is also considered a major pest in India, its native area, where it attacks fruit and cereal trees (Clergeau et al., 2015). It nests very early in tree cavities and seems to compete in certain regions with other cavity-dwelling species such as the Nuthatch, Sitta europaea (Strubbe and Matthysen, 2009). Studies also show potential impacts on Stock Doves, Columba oenas or bats (Hernandez-Brito et al., 2014) or on the feeding of small passerines (Peck et al., 2014) and during the breeding period, it displays aggressive behaviour towards other birds that fly around its nests (Clergeau et al., 2015).

Several works have already been carried out on the RRP all over the world and in Africa. In this context, we will cite for example the study on the introduction and nesting of the RRP in Algeria (Amina et al., 2005), and the study on the establishment of the RRP Psittacula krameri (syn: Alexandrinus parakeet) in Algeria and first data on its trophic ecology in this region (Bendjoudi et al., 2005). On the other hand, in Cameroon, no previous study has been carried out on RRP. This work was initiated with the overall objective of contributing to knowledge of the state of the RRP population with a view to its sustainable management in the city of Maroua. Specifically, it is: estimate the abundance and density of the Roseringed parakeet in the town of Maroua, map the spatial distribution of RRP; identify and assess the impact of different threats on this bird species.

Reference

Amina F, Moulaî R, Jacob JP. 2005. Introduction et nidification de la Perruche à collier (Psittacula krameri) en Algérie. Aves 42 (3), 257-262.

Bendjoudi D, Voisin JF, Doumandji S, Baziz B. 2005. Installation de la Perruche à collier Psittacula krameri dans l’Algérois et premières données sur son    écologie trophique dans cette région. Alauda 73, 329-334.

BirdLife International. 2018. Etat des populations d’Oiseaux dans le monde : prenons le pouls de la planète. Cambridge, UK : BirdLife International.

Blanco G, Hiraldo F, Tella JL. 2018. Ecological functions of parrots: an integrative perspective from plant life cycle to ecosystem functioning. Emu 118, 36–49.

Buckland ST, Anderson DR, Burnham KP, Laake JL. 2003. Distance sampling: estimating abundance of biological populations. Oxford University press, Inc., New York.

Clergeau P, Vergnes A, Delanoue R. 2008. La Perruche à collier Psittacula krameri introduite en Île-de-France : distribution et régime alimentaire. Muséum National d’Histoire Naturelle.

Clergeau P, Vergnes A, Delanoue R. 2009. La perruche à collier Psittacula krameri introduite en Ile-de-France : distribution et régime alimentaire. Alauda 77 (2), 121-132.

Clergeau P, Leroy O, Lenancker P. 2015. Dynamique de population de la perruche à collier Psittacula krameri introduite en Île-de-France. Alauda 83 (3), 165-174.

Earnst S, Holmes A. 2012. Bird-habitat relationships in interior Columbia Basin shrubsteppe. Condor 114 (1), 15-29. DOI: 10.1525/cond.2012.100176

Ellison AM, Bank MS, Clinton BD, Colburn EA, Elliott K, Ford CR. 2005. Loss of foundation species: consequences for the structure and dynamics of forested ecosystems. Frontiers in Ecology and the Environment 3, 479–486.

Grandi G, Menchetti M, Mori E. 2018. Vertical segregation by breeding ring-necked parakeets Psittacula krameri in northern Italy. Urban Ecosystem 21, 1011–1017. https://doi.org/10.1007/s11252-018-0779-1

Hernández-Brito D, Carrete M, Popa-Lisseanu AG, Ibañez C, Tella JL. 2014. Crowding in the city: losing and winning competitors of an invasive bird. PLoS One 9, e100593.

Jaquemet S. 2010. Rôle des Oiseaux marins tropicaux dans les réseaux trophiques hauturiers du sud et de l’océan Indien. Océan, Atmosphère. Université de la Réunion, Français.305P.

Kougoum, PGN, Tamungang SA, Téguia A. 2017. Breeding biology of African grey parrot (Psittacus erithacus) in Kom National Park (South-Cameroon) and implications to the species conservations. International Journal of Biological and Chemical Sciences 11(5), 1948-1966. https://doi.org/10.4314/ijbcs.v11i5.2

Kouzi P. 2012. Etat de connaissances bibliographiques de l’avifaune de Kisangani et ses environs (province Orientale, République démocratique du Congo). Mémoire master 2. Université de Kisangani.37Pp.

Le Gros A, Samadi S, Zuccon D, Cornette R, Braun MP, Senar JC, Clergeau P. 2016. Rapid morphological changes, admixture and invasive success in populations of ring- necked parakeets (Psittacula krameri) established in Europe. Biological Invasions 18, 1581-1598.

Madi OP, Sali B, Woin N. 2012. Utilisations et importance socio-économiques du Moringa oleifera au Maroua, Cameroun. Journal of Applied Biosciences 60, 4421– 4432.

Menchetti M, Mori E. 2014. Worldwide impact of alien parrots (Aves Psittaciformes) on native biodiversity and environment: a review. Ethology Ecology and Evolution 26, 172–194.

Mentil L, Battisti C, Carpaneto GM. 2018. The impact of Psittacula krameri (Scopoli, 1769) on orchards: First quantitative evidence for Southern Europe. Belgian Journal of Zoology 148(2). https://doi.org/10.26496/bjz.2018.22

Menchetti M, Mori E, Angelici FM. 2016. Effects of the recent world invasion by ring-necked parakeets Psittacula krameri. In: Angelici F (ed) Problematic Wildlife. Springer, Cham. https://doi.org/10.1007/978-3-319-22246-2_12

Mousa SD. 1994. Impact de la commercialisation de certaines espèces d’oiseaux au Sénégal. ORSTOM. 39p

Oumarou Y, Dapsia DJ, Ndih AC, Fameni TS, Haïwa G, Mohamadou A. 2022. Effets des fientes de volailles, du tourteau de neem [Azadirachta indica (A. Juss)] et du compost à base de bouse de bovin sur la croissance et le rendement du cotonnier (Gossypium hirsutum L.) et les propriétés phisico-chimiques du sol dans la localité de Zokok-Laddéo de la région de l’Extrême-Nord au Cameroun. Afrique Science 21(4), 138-149.

Parr M, Juniper T. 2010. Parrots: A guide to parrots of the world. Bloomsbury Publishing, London.

Peck HL. 2013. Investigating ecological impacts of the non-native population of Rose-ringed parakeets (Psittacula krameri) in the UK. PhD thesis, 212p.

Peck HL, Pringle HE, Marshall HH, Owens IP, Lord AM. 2014. Experimental evidence of impacts of an invasive parakeet on foraging behavior of native birds. Behavioral Ecology 25, 582–590.

Ricard J, Garcin A, Jay L, Mandrin J. 2017. Les Vertébrés, Biodiversité et regulation des ravageurs en arboriculture fruitiere. Centre technique interprofessionnel des fruits et légumes CtiffBalandran 30127 (France).33p.

Shiels AB, Kalodimos NP. 2019. Biology and impacts of Pacific Island invasive species. 15. Psittacula krameri, the Rose-Ringed Parakeet (Psittaciformes: Psittacidae). Pacific Science 73, 421–449.

Strubbe D, Matthysen E. 2009. Experimental evidence for nest-site competition between invasive Ring-necked Parakeets Psittacula krameri and native Nuthatches Sitta europaea. Biological Conservation 142, 1588-1594.

Vall-llosera M, Woolnough AP, Anderson D, Cassey P. 2017. Improved surveillance for early detection of a potential invasive species: the alien rose-ringed parakeet Psittacula krameri in Australia. Biological Invasions 19, 1273–1284. https://doi.org/10.1007/s10530-016-1332-x

Vangeluwe D. 2014. Rapport des activités et des résultats réalisés en 2014. Institut Royal des Sciences Naturelles de Belgique, Centre de baguage.

Weiserbs A. 2010. Invasive species: The case of Belgian Psittacidae. Impacts, risks assessment and range of control measures. Aves 47(1), 21-35.

Source : Population size and conservation management of the rose-ringed parakeet (Alexandrinus krameri) inthe town of Maroua, far north Cameroon  

Conservation Status of Tree Species in Tehsil Takht-e-Nasrati, Karak, Pakistan | InformativeBD

Conservation Status of Tree species in Tehsil Takht-e-Nasrati, Karak Pakistan

Musharaf Khan,  Farrukh Hussain , and  Shahana Musharaf, from the different institute of the Pakistan. wrote a research article about, Conservation Status of Tree Species in Tehsil Takht-e-Nasrati, Karak, Pakistan. entitled, Conservation Status of Tree species in Tehsil Takht-e-Nasrati, Karak Pakistan.This research paper published by the Journal of Biodiversity and Environmental Sciences(JBES). an open access scholarly research journal on Biodiversity. under the affiliation of the International Network For Natural Sciences | NNSpub. an open access multidisciplinary research journal publisher.

Abstract 

The present study documents the conservation status of 21 trees belonging to 14 families on small scale in Tehsil Takht-e-Nasrati, Karak through field surveys, frequently conducted in spring, summer and winter 2009-2010. Among these 9 species were found to be rare, vulnerable (6 species), Infrequent (3 species), endangered (one specie) and dominant (2 species). The conservation status of plants is determined according to IUCN 2001, Red Data List Categories and Criteria. After two years extensive field studies on the basis of questioner including availability of plant, collection of plant, growth of plant, plant parts, population size, geographic range and habitat we have concluded that Salvadora oleoides is endangered (EN) specie.

Submit your article to JBES Journal

Read moreSeed StorageImpact on Germination and Survival of Syzygium polycephaloides | InformativeBD

Introduction

The conservation status of organisms indicates whether the group is still extant or not and if yes, how likely the group is to become extant in the near future. Conservation status of a species depends upon many factors like grazing, fuel demand, agriculture land, deforestation, breeding success rates and known threats (Khan, et al., 2011). Based on the sample of species that have been evaluated through 2006, the percentage of endangered species as 40 percent of all organisms has calculated by the International Union for Conservation of Nature (IUCN) (Anon., 2008). Habitat loss and degradation, introduction of alien species, pollution and diseases, over-exploitation and climate change are some threats facing by plants which are an integral part of our ecosystem because native plants are key components of the global biological diversity (Sudhersan et al., 2003). It is estimated that some 270,000-425,000 vascular plant species are already known (Govaerts, 2001) with perhaps a further 10- 20% still to be discovered and described (Hawksworth & Kalin-Arroyo, 1995). Pakistan’s scenario is not different from the rest of the world. Plant biodiversity is also under tremendous pressure due to its population explosion, unplanned urbanization, deforestation and over-exploitation of natural resources. Unfortunately, very little work has been done on threatened plants of Pakistan and extremely limited information is available on this subject (Alam & Ali, 2009). According to Nasir (1991) 580-650 flowering plant species (i.e. 12%) are expected to be threatened. Chaudhri & Qureshi (1991) reported 709 taxa as threatened plants from Pakistan. However, both these studies are manly based on field observation and literature without any support of quantitative data. In contrast, the recent red list of IUCN (Anon., 2008) only 19 flowering plants species has been listed from Pakistan. Regarding Pakistan previous workers have classified the plant species as threatened or rare on the basis of literature or herbarium specimen. No work has been done according to IUCN red list categories or criteria (Anon., 2001) except Alam & Ali (2009), who classified Astragalus gilgitensis as a Critically Endangered (CR).

The Tehsil Takht-e- Nasrati is situated at o to 33.280 North and 70.300 to 71.300 East. The research area is bounded by Tehsil Karak on the North East, District Mianwali on the East, District Lakki Marwat on the South West and Tribal area Adjoining District Bannu on the West (Fig. 1). The total area of Tehsil is about 613.66 Sq. kilometers. Majority of the area consists of rigged dry hills and rough fields areas i.e. 323.97 Sq. kilometers and agriculture land is about 289.7 Sq. kilometers. The area is situated at 340 m above the sea level. The major problem of the area is shortage of drinking water and over grazing (Fig.2). The people bring drinking water from the remote area (Fig.3). In the year 2001 - 2010, 121.6mm of rainfall per 10 year recorded. The area is very hot in summer and very cold in winter. June and July are the hottest months, whereas December and January are the coldest months. In the year 2001 - 2010 the mean maximum temperature was 39.5o C, in the month of the June, where as the mean minimum temperature was as low as 4.26o C, in the month of January (Table.1). Write down the aim and necessity of your study here.

Reference

Alam J, Ali SL. 2009. Conservation status of Astraglus gilgitensis Ali (Fabaceae): a critically endangered species in Gilgit district, Pakistan. Phyton (Horn, Austria) 48(2), 211-223.

Anonymous. 2001. IUCN Red List Categories: Version 3.1. Species Survival Commission. IUCN, Gland, Switzerland & Cambridge, UK.

Anonymous. 2008. IUCN Red List of threatened species, www.iucnredlist.org cited on December 27th 2009.

Baggs JE, Maschinski J. 2000. Annual report on the long-term research on Purshia subintegra in the Verde Valley for 1999. Report to Arizona Department of Transportation, Phoenix, Arizona, USA.

Chaudri MN, Qureshi RA. 1991. Pakistan’s Endangered Flora –II. Pakistan Systematics 5 (1- 2), 1-84.

Davis SD, Heywood VH, Hamilton AC. 1995. Centres of Plant Diversity: a guide and strategy for their conservation, Vol. 2 (Asia, Australasia and the Pacific). Cambridge: IUCN.

El-Keblawy A, Al-Rawai A. 2007. Impacts of the invasive exotic Prosopis juliflora (Sw.) D.C. on the native flora and soils of the UAE. Plant Ecology 190 (1), 23-35.

Engler M. 2008. The Value of International Trade. Traffic Bulletin 22(1), 4-5.

Govaerts R 2001. How many species of seed plants are there? Taxon 50(4), 1085-1090.

Hawksworth DL, Kalin-Arroyo MT. 1995. Magnitude and distribution of biodiversity. In: Global Biodiversity Assessment. (Ed.): V.H. Heywood. Cambridge University Press, Cambridge, UK; 107-192.

Hirway I, Goswami S. 2007. Valuation of Coastland Resources. The Case of Mangroves in Gujrat. Academic Foundation. India.

Huston MA. 1994. Biological Diversity: The Coexistence of Species on Changing Landscape. Cambridge University Press, Cambridge.

Khan  M,  Shinwari  ZK,  Musharaf  S.  2011. Conservation and ecological characteristic of Trees in Tehsil Karak Pakistan, J. Bio. & Env. Sci. 1(6), 155-164.

Kruckeberg AR, Rabinowitz D. 1985. Biological aspects of endemism in higher plants. Annual Reviews of Ecological Systematics 16, 447-479.

Myers N. 1988. Threatened Biotas: “Hotspots” in tropical forests. Environmentalist 8, 1-20.

Nasir YJ. 1991. Threatened plants of Pakistan. In: Plant Life of South Asia. (Eds.): S.I. Ali & A. Ghaffar. Shamim Press, Karachi; 229-234.

Noor M, Salam U, Khan MA. 1995. Allelopathic effects of Prosopis juliflora Swartz. Journal of Arid Environments 31(1), 83-90.

Pallewatta N, Reaser JK, Gutierrez AT. 2003. Invasive alien species in South-Southeast Asia: National Reports & Directory of Resources. Global Invasive Species Programme, Cape Town, South Africa.

Pieper RD. 1994. Ecological implications of livestock grazing. In: Ecological Implications of Livestock Herbivory in the West. (Eds.): M. Vavra, W.A. Laycock and R.D. Pieper. Society for Range Management, Denver, CO. 177-211.

Primental D, Lach L, Zuniga R, Morrison D. 2000. Environmental and economic costs of non-indigenous species in the United States. Bioscience 50, 53-65.

Rabinowitz D. 1981. Seven forms of rarity. In: The Biological Aspects of Rare Plant Conservation. (Ed.): H. Synge. Wiley & Sons Ltd. 205-217.

Sudhersan C, Abo El-Nil M, Hussain J. 2003. Tissue culture technology for the conservation and propagation of certain native plants. Journal of Arid Environments 54, 133-147.

SourceConservation Status of Tree species in Tehsil Takht-e-Nasrati, Karak Pakistan