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ABSTRACT
The Kirthar Formation in Mach area of the Sulaiman Fold-Thrust Belt (SFTB) has yielded rich but moderately diverse larger benthic
foraminiferal assemblage, comprising of thirty species from nineteen genera, suggesting a late Middle Eocene to Late Eocene (SBZ 18-
SBZ 20) age. The late Middle Eocene (SBZ 18) is recognized by the co-occurrence of Pellatispira madraszi, Nummulites maximus,
Borelis vonderschmitti, Nummulites chavannesi, Discocyclina discus, Discocyclina preaomphalus, Silvestriella tetraedra, Asterocyclina
sireli and Asterocyclina stellata. The boundary between Middle and Late Eocene is marked by the first occurrence of Nummulites
fabianii and the disappearance of typical Bartonian taxa such as Nummulites maximus, Discocyclina discus, Discocyclina preaomphalus,
Asterocyclina sireli, Asterocyclina stellata.
KEYWORDS: Larger Benthic Foraminifera; Biostratigraphy; Eocene; Kirthar Formation; Sulaiman Fold-Thrust Belt.
Based on his diverse assemblages the formation has been dated Most of the geology and tectonics of Pakistan including
as Early Eocene to Early Oligocene. Recent studies based on Western Fold-Thrust Belt (WFTB) owes to the head on
some planktonic and smaller benthic foraminifera in parts of collision of Indo-Pak plate with Eurasian Plate at its
southern Sindh such as Sukkur and Kotdigi also suggests northwestern margin (Molnar and Tapponier, 1975; Powell,
Middle Eocene to lower Oligocene age (Usmani et al., 2008). 1979; Bordet, 1978; Acharyya, 1979; Bingham and Klootwijk,
However, despite the wide geographic extension of the Kirthar 1980). The collision occurred around 55 Ma, Muslim Bagh-
Formation and its high vertical thicknesses, it is least studied in Zhob Ophiolite pops out in the Zhob valley, which is considered
terms of foraminifera and lacks the modern biostratigraphic to be the relics of oceanic crust of the eastern Tethys Ocean
framework as compare to their Eocene counterparts of the of obducted onto the western passive margin of Indo-Pak plate
the Kohat and Potwar plateaus in Pakistan (Ahmad et al., 2014; around 65 Ma, which indicates the initial collision of plates
Ahmad et al., 2016). In Mach area, Kirthar Formation has never (Alleman, 1979; Gnos et al., 1996; Kakar et al., 2012). After
been studied for foraminifera and here an attempt has been the initial collision of Indian plate, since the collision was
made to (a) document the foraminiferal fauna of the Kirthar oblique, a remnant Tethys Ocean was formed in the west of
Formation in the study area (b) establish biostratigraphic SFTB (Pishin Belt) in Eocene, which was receiving detritus
foraminiferal zones on the basis of recovered foraminiferal from evolving Himalayas through Palaeo Indus River (Qayyum
assemblages. et al., 1996; Kasi et al., 2018). After the complete suturing and
uplifting of Pishin belt the drainage was diverted towards the
Tectonic Settings
foreland and fordeeps of Sulaiman and Kirthar belts and thick
The fold and thrust belts of western Pakistan comprises Himalayan sourced molasses succession was deposited in
Sulaiman and Kirthar belts. They are the south and Oligocene- Miocene. The Indus River is presently depositing
southwestern extension of Himalayas (Bannert, 1992; Bender sediments in Punjab and Sindh plains. In Miocene-Pliocene
and Raza 1995; Kazmi and Jan, 1997). Main Boundary and Salt period the thick locally derived Urak and Sibi groups molasses
Range thrusts of sub Himalayas bound the SFTB in the north. were deposited in the inter-mountain basins within the SFTB
The SFTB is southward-convex arcuate belt characterized by (Kassi et al., 2009).
east-west trending folds. Kirthar Fold-Thrust Belt (KFTB) and
Indus plain bound the belt in the south. The Quetta Syntaxis is MATERIAL AND METHODS
a hairpin tight bend which separates the SFTB from KFTB. The
Pishin Belt and left lateral strike slip Chaman Fault are located The studied section of the Kirthar Formation is located at about
farther west (Lawrence et al., 1981; Patrait and Achache, 1984; 2.5 km in the east of Mach town (N 29° 51ʹ 25ʺ; E 67° 21ʹ 3ʺ)
Basse and Courtillet, 1988; Searle et al., 1997). The SFTB was measured and sampled. This section is 106 m thick,
gradually lose its amplitude at frontal foredeeps and submerges comprising of medium to thick bedded, nodular limestone. A
into Indus plain. It comprises over 10 km thick Triassic to total of forty-five samples with an average interval of about 1
Pleistocene sediments with some volcanic and volcaniclastic to 2 m were collected. The rock samples were thin sectioned
succession (e.g. Bibai Formation; Kazmi, 1979; Khan et al., and photographed in plane polarized light with a digital camera
1999) (Fig. 2). (C-35AD-2) attached to an Olympus Microscope (BH-2) in the
Centre of Excellence in Mineralogy, University of Balochistan,
Quetta.
BIOSTRATIGRPAHIC RESULTS
Fig. 2. Generalized geological and Tectonic map of the South- These biozones are mainly derived from the ranges of the LBF
West Pakistan. The study area is in extreme western proximity recovered from the western Tethyan region and some parts of
of Suleiman Ranges representing Quetta syntaxes. (After Kasi the eastern Tethys such as Pakistan and India which were
et al., 2012). comparatively least studied (Cahuzac and Poignat, 1997; Serra-
Kiel et al., 1998). However, the recent studies in the last decade
Page 2 © BURJES ISSN 2415-2234
Bahria University Research Journal of Earth Sciences Vol. 4 (1), 2019
in various parts of the eastern Tethys have revealed some faunal Most of these species such as Pellatispira madraszi, Borelis
differences linked to India-Asia collision (Afzal et al., 2009; vonderschmitti, Nummulites chavannesi have their first
2011a; Zhang et al., 2013; Ahmed et al., 2016). These faunal appearance in SBZ 18, whereas Nummulites maximus has its
differences are particularly noticed in the Palaeocene and last occurrence in SBZ 18 (Banerji, 1981; Serra-Kiel et al.,
Eocene, demonstrated to have been due to some biogeographic 1998; Rasser et al., 1999; Özcan et al., 2010; Less and Özcan,
barriers between eastern and western Tethys, which gave rise to 2012; Costa et al., 2013; Cotton et al., 2016). Similarly, species
non-synchronous evolution (Afzal et al., 2011a, 2011b; Zhang such as Discocyclina discus, Discocyclina preaomphalus,
et al., 2013; Kahsnitz et al., 2016). However, there are many Asterocyclina sireli, Asterocyclina stellata are reported from
cosmopolitan taxa which can be used to correlate the the Bartonian of the western as well as the eastern Tethys and
Palaeogene strata throughout Tethys. there is no evidence of their occurrence in Late Eocene (Özcan
et al., 2010, 2016; Less et al., 2011; Ali et al., 2018). Late
The Kirthar Formation in Mach area of the western part of the Eocene is identified by the first appearance of Nummulites
Sulaiman Belt has yielded rich faunal assemblage comprising fabianii and cannot be further divided in to SBZ 19 and SBZ 20
of thirty species from nineteen different genera, suggesting a due to lack of index taxa. Other associated species include
late Middle Eocene (SBZ 18) to Late Eocene age for the Kirthar Asterigerina rotula, Medocia blayensis, Borelis vonderschmitti
Formation in the study area. Late Middle Eocene (SBZ 18) and species of Silvestriella, Sphaerogypsina, and
identified by the presence of Pellatispira madraszi, Nummulites Quinqueloculina. Nummulites fabianii is a common index
maximus, Borelis vonderschmitti, Nummulites chavannesi, species of the Late Eocene and is documented from various
Discocyclina discus, Discocyclina preaomphalus, Asterigerina regions of eastern and western Tethys (Meinhold and
rotula, Linderina brugesi, Silvestriella tetraedra, Asterocyclina Boudagher-Fadel, 2010; Özcan et al., 2010; Less et al., 2011;
sireli, Asterocyclina stellata, Medocia blayensis, Meghalayana Bukhari et al., 2016). A detailed biostratigraphic species log is
indica, and taxa which typifies only Late Eocene are not found given (Fig. 3) and their micro-photograph plate presented in
in this assemblage. Fig. 4.
Fig. 3. Biostratigraphic log showing the species distribution and diversity in Kirthar Formation at Mach Jalal Abad, section.
Fig 4. The micro-photograph plate of fossils.1-3, Asterigerina rotula, 1, MJK-10; 2, MJK-19; 3, MJK-17. 4-6, Medocia blayensis, 4,
MJK-30; 5, MJK-10; 6, MJK-2. 7-8. Asterocyclina sireli, 7. MJK-2; 8, MJK-6. 9-10, Asteocyclina stellata, 9, MJK-3; 10, MJK-6. 11-
12, Asterocyclina spp., 11, MJK-6; 12, MJK-1. 13-14, Discocyclina discus, 13, MJK-2; 14, MJK-6. 15-16, Discocyclina dispansa, 15,
MJK-3; 16, MJK-4. 17, Discocyclina praeomphalus, MJK-7. 18-19, Discocyclina spp., 18, MJK-4: 19, MJK-6. 20, Glomalveolina sp.,
MJK-18. 21-22, Borelis vonderschmitti, 21, MJK-44; 22, MJK-45. 23-24, Linderina brugesi, 23, MJK16; 24, MJK-26. 25-26,
Sphaerogypsina spp., 25, MJK-19; 26, MJK-20. 27-28, Pyrgo spp., 27, MJK18; 28, MJK-25. 29-30, Quinqueloculina spp., 29, MJK-
33; 30, MJK-43. 31-33, Operculina spp., 31, MJK-3; 32, MJK-5; 33, MJK-2. 34-35, Meghalayana indica, 34, MJK-9; 35, MJK-11.
36-37, Silvestriella tetraedra, 36, MJK-5; 37, MJK-26. 38-39, Silvestriella spp., 38, MJK-6; 39, MJK-35. 40-43, Heterostegina spp.,
40, 42, MJK-9; 41, MJK-4; 43, MJK-12. 44-45, Nummulites maximus, 44, MJK-7; 45, MJK-9. 46-47, Nummulites Chavannesi, 46,
MJK-6; 47, MJK-9. 48-50, Nummulites fabianii, 48, MJK-35; 49, MJK-39; 50, MJK-40. 51-56, Nummulites spp., 51, 56, MJK-40; 52,
MJK-39; 53, 55, MJK-6; 54, MJK-9. 57-59, Pellatispira madraszi, 57, MJK-19; 58, MJK-18; 59, MJK-17. 60-61, Pellatispira spp.,
60, MJK-34; 61, MJK-10. (3-6,21-30,44-47) Scale bar 200 µm; (1-2, 7-20,31-43,48-61) Scale bar 500 µm.
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