ABSTRACT
Past climate reconstructions from palaeoecological records require an understanding of relationships between modern vegetation and climate. Phytoliths are being used widely to reconstruct variations in C3/C4 grasses in the past vegetation and corresponding climate. However, little understanding is available on their relationships with the climate driver(s). Even though, the driver(s) regulating C3/C4 grass distributions vary regionally, while reconstructing the past distributions, a grass phytolith-based climatic index (Ic) has often been found to be used globally without assessing its regional consistency. In the Himalaya, the working potential of Ic has proven to be unsatisfactory when compared to other regions of the globe. To improve the efficacy of Ic, we have identified the redundant grass phytolith morphs and revised it by including four exclusive C3-grass indicator morphotypes (bilobate trapezoidal, bilobate scooped, saddle tall and saddle plateaued) to the existing Ic calculation. Thus, a new climatic index, revised Ic (rIc) is proposed in this article. We have compared the rIc with modern climate variables and a relationship with mean annual temperature (MAT) is established with statistical validation. To assess the working potential of the proposed calibration function in the past temperature reconstructions, we have estimated the late Holocene MAT variations in the Himalaya using rIc. We infer that in the mountainous regions like the Himalaya, even with irregular precipitation distribution, variability in C3/C4 grass distributions and their phytolith spectra seem to be a primary function of temperature. Further, we recommend that rIc can be satisfactorily used to reconstruct past temperature variations in the Himalaya and similar mountainous regions where soil water availability is not a limiting factor.
ABSTRACT
A rich and diverse palynoassemblage recovered from the Churanthi River section (26°53' 59.3" N, 88°34' 17.2" E), Darjeeling foothills Eastern Himalaya, has yielded 87 species assigned to 69 genera. The palynoassemblage is rich in angiosperm taxa (45.63%) followed by gymnosperms (0.45%), pteridophytes (18.49%) and fungal remains (23.88%). Based on their nearest living relatives, a wet evergreen to semi-evergreen forest under a humid tropical to sub-tropical environment during the Mio-Pliocene age has been suggested. A lot of angiosperms such as Palaeosantalaceaepites, Araliaceoipollenites, Malvacearampollis, Zonocostites, Neocouperipollis, Dicolpopollis, Palmidites, Palmaepollenites, isolated salt glands of mangrove plant leaves (Heliospermopsis) and Mediaverrunites type of fungal spores, along with ichnofossils like Planolites, Palaeophycus, Skolithos, Rosselia, Ophiomorpha and Teichichnus associated with rippled mudstone-siltstone suggest an environment strongly influenced by brackish water. Primary sedimentary structures in the associated strata indicate strong wave agitation common in shallow marine setting. Some high elevation components (5.14%) such as Alnipollenites, cf. Corylus (Betulaceae), Juglanspollenites, Engelhardtioipollenites (Juglandaceae), Quercoides, Cupuliferoidaepollenites, Lithocarpus, Castanopsis (Fagaceae), Abietineaepollenites (Pinaceae) represent hinterland vegetation possibly transported to the prograding deltaic coastline by the rivers. Reworked palynotaxa (Striatopodocarpites sp., Striatites sp., Faunipollenites sp., Circumstriatites sp., Crescentipollenites sp., Cuneatisporites sp., Parasaccites sp., Scheuringipollenites sp., Rhizomaspora sp., Marsupipollenites sp., Lophotriletes sp.) of Permian age have also been recorded in the palynoassemblage (11.55%) indicating the abundance of Permian Gondwana strata in the source area.
