Page 62

Proceedings of International Conference on Climate Change, Biodiversity and Ecosystem Services for the Sustainable Development Goals : Policy and Practice 27-29 June 2016 at the Sirindhorn International Environmental Park, Cha-am, Phetchaburi, Thailand

Propagules  of  collected  plants  (each  population)  were  raised  from  root  cuttings  and  plants  were  grown  in  the  greenhouse  of  Botanical  Garden,  Department  of  Botany,  Annamalai  University,  Annamalai  Nagar,  Tamil Nadu.  Stem  cuttings  were  collected  from  15  Table  1  Populations  and  collection  details  of  Gloriosa  superba  from  the  study  area The  plant  samples  were  collected  from  ten  populations  of  the  d i ff e r e n t  geographical  positions  of  South  India.  Such  as  Udaiyarpalaiyam,  Yelagiri  Hills,  Pallakkodu,  Kalrayan  Hills,  Nagercoil,  Bhavani,  Mandya,  Bangalore,  Kozhikode  and  Kottayam. Morphological  characterization Morphological  features  utilized  for  characterization  were  plant  height,  number  of  branches/plant,  leaf  length,  leaf  width,  number  of  flowers  per  cyme,  number  of  fruits  per  cyme,  tuber  length  and  tuber  yield. Assessment  of  alkaloid  content  of  various  populations  of  Gloriosa  superba Total  alkaloid  contents  were  estimated  from  tubers  of  Gloriosa  superb  collected  from  different  habitats.  100  g  of  powdered  dry  samples individuals  of  each  population.  Individuals  were  chosen  at  random  and  young  shoots  were sprouted  from  the  cuttings  after  one  month  of  planting.  From  each  population,  10  individuals  each  were  selected  for  molecular  genetic  analyses. of  Gloriosa  superb  was  soaked  in  200  mL  methanol  and  left  for  30  min.  After  30  min,  the  soaked  plant  material  was  filtered.  The  residue  obtained  after  filtration  is  further  dissolved  in  5  mL  methanol  and  filtered.  After  10  mins,  the  same  step  is  repeated  once  again  and  the  final  filtrate  is  collected  in  50  mL  conical  flask.  The  extract  was  evaporated  to  dryness  in  the  Soxhlet.  evaporator.  The  crude  extract  was  dissolved  in  100  mL  of  0.01 M  HCl.  The  pH  of  filtered  solutions  was  adjusted to  6.0  with  0.01 M  NaOH.  The  crude  extracts  obtained  were  used  for  HPLC  analysis  6.  The  crude  extract  obtained  was  concentrated  to  dryness  to  yield  crude  alkaloid  fraction  (CAF). The  extract  of  each  plant  was  transferred  to  5  mL  volumetric  flasks  separately  with  the  help  of  methanol  (HPL  Cgrade),  sonicated  for  a  few  minutes  and  filtered  and  the  volume  was made up  to  mark  with  methanol;  0.004%  of  Colchicine  in  methanol  was  used  as  standard. 60 Proceedings  of  the  International  Conference  on  Climate  Change,  Biodiversity  and  Ecosystem  Services  for  the Sustainable  Development  Goals  (SDGs):  Policy  and  Practice  27-29  June  2016,  Cha-am,  Phetchaburi,  Thailand


Proceedings of International Conference on Climate Change, Biodiversity and Ecosystem Services for the Sustainable Development Goals : Policy and Practice 27-29 June 2016 at the Sirindhorn International Environmental Park, Cha-am, Phetchaburi, Thailand
To see the actual publication please follow the link above