Professional Documents
Culture Documents
Paleoecología de la facies grainstone rica en algas rojas coralinas del Mioceno Inferior de la
Formación Qom (sección Vartun, Irán central)
ABSTRACT
Amir Hossein Rahiminejad1,*, Mehdi Yazdi2, Amit Kumar Ghosh3
1
Department of Ecology, Institute of Science ABSTRACT RESUMEN
and High Technology and Environmental Sci-
ences, University of Advanced Technology,
Kerman, Iran. In this paleoecological study we focused on En este estudio paleoecológico se enfocó en las
coralline red algae-rich shoal grainstone facies facies grainstone rica en algas rojas coralinas en
2
Department of Geology, Faculty of Sciences, in the Lower Miocene (Aquitanian) carbon- los carbonatos del Mioceno Inferior (Aquita-
University of Isfahan, Isfahan 81746-73441, ates of the Qom Formation in the Vartun sec- niano) de la Formación Qom en la sección Var-
Iran. tion in central Iran. The identified coralline tun del centro de Irán. Las algas rojas coralinas
red algae are mainly non-geniculate, although identificadas en las facies son principalmente
3
Birbal Sahni Institute of Palaeosciences, 53 very rare geniculate forms of corallines were no geniculadas, aunque también se caracteri-
University Road, Lucknow-226 007, Uttar also recognized in thin section analysis. The zaron formas geniculadas mediante análisis de
Pradesh, India. identified algae are represented by Melobesi- láminas delgadas. Las algas identificadas están
oideae (Lithothamnion cf. valens, Lithothamnion cf. representadas por Melobesioidea (Lithothamnion
rovereoti, Lithothamnion cf. peleense, and Lithotham- cf. valens, Lithothamnion cf. rovereoti, Litho-
* Corresponding author: (A.H. Rahiminejad) nion spp.), Mastophoroideae (Neogoniolithon thamnion cf. peleense, y Lithothamnion spp.),
ah.rahiminejad@kgut.ac.ir sp., Spongites spp., and Spongites cf. fruticulosus), Mastophoroidea (Neogoniolithon sp., Spongites
Sporolithon spp. (Sporolithon spp. and Sporolithon spp., y Spongites cf. fruticulosus), Sporolithon
cf. airoldii), and geniculate coralline (Corallina). spp (Sporolithon spp. y Sporolithon cf. airoldii),
The algal taxa mainly display fruticose and y por coralinas geniculadas (Corallina). Los
lumpy growth forms. The dominance of the taxones de algas muestran principalmente for-
former is consistent with high water energy mas grandes y grumosas de fructicoso. Donde
in the identified shoal environment. The predomina consistentemente con alta energía del
presence of Lower Miocene algae indicates agua en el ambiente arrecifal identificado. La
that deposition of carbonates took place presencia de algas del Mioceno Inferior indica
in warm tropical to subtropical waters in a que la exposición de carbonatos tuvo lugar en
euphotic marine environment during the aguas cálidas tropicales a subtropicales en la
Aquitanian. Likewise, high water energy and zona eufótica marina durante el Aquitaniano.
sediment agitation resulted in taphonomic Asimismo, tanto la alta energía del agua como
features such as fragmentation, abrasion, and la agitación de los sedimentos, dieron lugar a
disarticulation. características tafonómicas tales como fragmen-
tación, abrasión, y desarticulación.
Figure 1 (A) Geological and structural map of Iran and location of the studied section (Vartun section) in the north of the Esfahan–Sirjan
Basin in central Iran (modified from Rahiminejad and Hassani, 2016; Rahiminejad et al., 2017, 2018; Rahiminejad and Zand-Moghadam,
2018, 2020; Moosavizadeh et al., 2020). (B) Location map of the Vartun section (modified from Zágoršek et al., 2017). (C) Geological map
of the studied area (redrawn and modified from Zahedi, 1978 and Rahiminejad et al., 2020).
http://dx.doi.org/10.18268/BSGM2022v74n2a020122
Roozpeykar et al., 2019a). This paper focuses on the Qom Formation in the Esfahan–Sirjan Basin
the paleoecological aspects of Lower Miocene are consistent with mixed carbonate–siliciclastic
coralline red algae from the Qom Formation and homoclinal ramp (Reuter et al., 2009), open shelf
contributes data from the algal-rich Cenozoic car- (SE Chahriseh (Moradi, 2012)), and inner and
bonates of Iran. middle ramps Vartun section (Rahiminejad et al.,
2020).
2. Geological Setting
3. Materials and Methods
In the present study, samples yielding fossil cor-
alline red algae were collected from the Lower The investigation of fossil coralline red algae and
Miocene Qom Formation in the Vartun section their associated facies or sedimentary texture was
(Figures 1 and 2). This section is located about 50 based on microscopic analyses of thin-section
km northeast of the city of Esfahan (32° 56′ 13.79″ slides from thirty rock samples of algal limestone
N and 52° 08′ 45.32″ E; Figure 1) and is situated in that were examined with a Stereo binocular Micro-
the north of the Esfahan–Sirjan fore-arc basin in scope model Yaxun YX AK21 and photographed
central Iran (Figure 1A). The most exposed strata using a CCD digital camera model KECam. The
in the studied area comprise Quaternary terraces classification of carbonate facies followed that of
in addition to Triassic (massive dolomite, dolo- Dunham (1962) and Flügel (2010), which is based
mitic limestone, limestone, shale), Jurassic (sandy on the types and abundance of grains and the
shale, sandstone, conglomerate), and Oligocene– matrix in the deposits. Taxonomic analysis of the
Miocene deposits (Figure 1C). Strata of the Qom identified coralline red algae was based on Braga
Formation were deposited on the northeastern (2003), Brandano and Piller (2010), and Sarkar
edge of the Tethyan Seaway in the Sanandaj–Sir- (2017). Coralline red algal growth forms were
jan fore-arc basin, and/or Esfahan–Sirjan fore- described according to Woelkerling et al. (1993),
arc basin, and the Urumieh–Dokhtar magmatic and Nebelsick and Bassi (2000).
arc basin in central Iran during the last marine Since the collected algal specimens in the
transgression in the Oligo–Miocene (Daneshian studied section are present as bioclasts and par-
and Ramezani Dana, 2007; Reuter et al., 2009; tially preserved fossils, confirmation of taxa at
Zágoršek et al., 2017). the species level cannot be accurately established.
Figure 2 Measured stratigraphic column of the Qom Formation in the Vartun section. Age of the Qom Formation in the section is based
on Rahiminejad et al., 2020. Our studies focused on a 1 m-thick interval algal limestone comprising coralline red algae-rich grainstone.
The symbols illustrating the growth forms of the identified algae are redrawn and modified from Woelkerling et al., (1993), and
Nebelsick and Bassi (2000). The percentage or relative abundance of different algal growth forms in the studied grainstone facies is as
follows: fruticose: 70 %, lumpy: 20%, foliose, encrusting, and arborescent: 10%.
http://dx.doi.org/10.18268/BSGM2022v74n2a020122
RESULTS
Miocene coralline red algae from the Qom Formation
Figure 3 Some of the identified large benthic foraminifera used for age determination of the Qom Formation in the Vartun section
(Rahiminejad et al., 2020). (A) Lepidocyclina sp., (B) Nephrolepidina sp., (C) Eulepidina sp., (D) Operculina spp., (E) Miogypsina sp., (F)
Amphistegina sp. Note that these microfossil specimens were not collected from the algal grainstone facies in this study.
http://dx.doi.org/10.18268/BSGM2022v74n2a020122
Figure 4 (A) Outcrop view of the studied coralline red algae-rich limestone (1 m thick) in a grainstone facies. (B) Rock sample of the
studied algae-rich limestone.
massive and lithified coralline red algae-rich lime- of corals, echinoids, gastropods, and bivalves
Miocene coralline red algae from the Qom Formation
stone in the Qom Formation (Figures 2 and 4). (22%) as well as scarce (13%) larger benthic for-
The stratigraphic details of the Qom Formation aminifera (Nephrolepidina sp., Amphistegina sp., and
in the studied section are shown in Figure 2. In the miliolids) comprise the subordinate skeletal grains.
field, the limestone interval (Figures 2 and 4) is lat-
erally exposed up to ca 70 m, is discontinuous, and 4.2. THE IDENTIFIED CORALLINE RED ALGAE AND
untraceable in a wide area. Cylindrical Skolithos THEIR GROWTH FORMS
burrows are common and fossils of bivalves (pec-
tinids), gastropods (Conus, Natica, and Pleurotomaria), The micropaleontological studies revealed the
and echinoids (Clypeasteroids) are abundant in the presence of five genera of coralline red algae in
interval (Figure 2). Likewise, the limestone interval the studied grainstone facies (Table 1 and Figures
is composed of coralline algae-rich grainstone 5 to 8). Non-geniculate forms of the identified
facies dominated by skeletal grains embedded in a algae predominate (Table 1), whereas algae rep-
sparitic matrix or sparry cement (Figures 5A and resentative of geniculate forms (genus Corallina)
5B). The latter (65%) include coarse-grained bio- are scarce. Several of the non-geniculate algae are
clasts and partially preserved specimens of abun- highly fragmented and abraded, while geniculate
dant coralline red algae. Coarse-grained bioclasts forms are disarticulated and fragmented. The
http://dx.doi.org/10.18268/BSGM2022v74n2a020122
percentage or relative abundance of the algae is with foliose, encrusting, and arborescent growth
indicated in Table 1. The non-geniculate algae forms are also present (Table 1), although subor-
include melobesioids, mastophoroids, and sporo- dinately (10%).
lithaceans (Table 1). Melobesioids comprise the
taxa Lithothamnion cf. valens, Lithothamnion cf. rove-
reoti, Lithothamnion cf. peleense, and Lithothamnion spp. 5. Discussion and interpretation
Mastophoroids are represented by the taxa Neogo-
niolithon sp., Spongites cf. fruticulosus, and Spongites 5.1. PALEOECOLOGY OF THE IDENTIFIED
spp. Sporolithaceans include the taxa Sporolithon CORALLINE RED ALGAE
spp., and Sporolithon cf. airoldii.
In the studied grainstone facies, the identified The dominance of a sparitic matrix or sparry
coralline red algae mainly display fruticose (70 %) cement in the identified algal grainstone facies
and lumpy (20%) growth forms (Table 1). Algae and the abundance of bioclasts and skeletal grains
http://dx.doi.org/10.18268/BSGM2022v74n2a020122
DISCUSSION AND INTERPRETATION
Table 1. The identified coralline red algae and their growth forms in the algal grainstone facies. The algae are dominated by non-
geniculate forms. Geniculate forms (Corallina sp.) of the algae are scarce. The percentage or relative abundance of different growth
forms of the algae in the studied grainstone facies is as follows: fruticose: 70 %, lumpy: 20% foliose, encrusting, and arborescent: 10%.
Corallina
Corallina : 5% Arborescent
point to a shoal environment (in an inner ramp) in instance, Ghosh and Sarkar (2013) have reported
a high-energy water zone above the fair-weather a grainstone facies comprising an algal associa-
wave base during the Aquitanian (Flügel, 2010; tion of Corallina, Lithothamnion, and Spongites from
Sadeghi et al., 2011; Vescogni et al., 2014; Rooz- Pliocene reef and back-reef shelf environments
peykar et al., 2019b). as well as a melobesioid coralline algal assemblage
The presence of Skolithos burrows in the algal of Phymatolithon, Mesophyllum, and Lithothamnion
grainstone-bearing limestone indicates high from a coralline algal boundstone in a Pliocene
hydrodynamic (water) energy (Vinn and Wilson, fore-reef environment. Roozpeykar et al. (2019a,
Miocene coralline red algae from the Qom Formation
2013; Sedorko et al., 2018). Further details on the 2019b) have studied a coralline red algae-rich
depositional environment of the Lower Miocene grainstone in a Miocene shoal environment in the
deposits of the Qom Formation in the Vartun Zagros Basin and have reported non-geniculate
section have been provided by Rahiminejad et al. (dominant Spongites and reworked melobesioids)
(2020), whose results confirm our environmental and geniculate algae (Corallina).
interpretation. Generally, coralline red algae were one of the
The co-occurrence of melobesioids (Lithotham- major and most abundant’biotic components of
nion), mastophoroids (Neogoniolithon, Spongites), and photozoan and heterozoan communities of Oligo-
Sporolithon may be representative of the basinward cene–Miocene cool waters (non-tropic) and trop-
part of the shoal environment, although a num- ical carbonates (Bassi and Nebelsick, 2010; Braga
ber of these algae could have been reworked and et al., 2010). Mastophoroids (specifically Spongites)
transported in the shoal environment. are common in shallow tropical carbonates (Adey
Usually, the occurrence of coralline red algae et al., 1982; Braga and Aguirre, 2001, 2004), but
in a grainstone facies is related to nutrient influx are also present in subtropical and temperate
due to encroachment of siliciclastics (Erlich et environments. Some genera (e.g. Lithothamnion and
al., 1990, 1993; Roozpeykar et al., 2019a). For Mesophyllum) of the subfamily Melobesioideae
http://dx.doi.org/10.18268/BSGM2022v74n2a020122
Figure 6 Identified coralline red algae in the grainstone facies. (A) Fragment of Sporolithon sp. showing a lumpy growth form. (B)
occur in both temperate and warm conditions hydrodynamic energy, chemical composition,
(Braga and Aguirre, 2001; Halfar and Mutti, 2005; light intensity, and temperature of marine waters
Bassi et al., 2009; Braga et al., 2010; Brandano and (Sarkar, 2017). The different growth forms of
Piller, 2010; Rösler et al., 2015; Roozpeykar et al., coralline red algae are useful tools in paleoeco-
2019a, 2019b). Also, sporolithaceans (Sporolithon) logical interpretation of marine carbonate facies
are common in tropical deposits (Brandano et al., (Bosence and Pedley, 1982; Braga and Martín,
2005). Coralline red algae can survive in different 1988; Braga and Aguirre, 2001; Rasser and
trophic conditions ranging from oligotrophic to Piller, 2004; Brandano et al., 2005; Brandano and
mesotrophic environments in different latitudes Ronca, 2014) and include warty, lumpy, fruticose,
(Braga et al., 2010). The main paleoecological foliose, encrusting, layered (non-geniculate), and
factors controlling their growth and development arborescent (geniculate) (Woelkerling et al., 1993;
in benthic marine environments include depth, Nebelsick and Bassi, 2000).
http://dx.doi.org/10.18268/BSGM2022v74n2a020122
DISCUSSION AND INTERPRETATION
Figure 7 Identified coralline red algae in the grainstone facies. (A) Lumpy growth form of Lithothamnion cf. rovereoti. (B) Fragment of
Miocene coralline red algae from the Qom Formation
a fruticose thallus of Lithothamnion sp.; partially abraded. (C) Fragment of fruticose thalli of Lithothamnion cf. peleense. (D) Fruticose
thallus of Lithothamnion sp. (E) Foliose thalli of Lithothamnion sp.
As evidenced in this study, the dominance of cor- marine zone (Vescogni et al., 2014; Roozpeykar
alline red algae with fruticose growth forms (Table et al., 2019a, 2019b). The overall recognition of
1) in the shoal carbonate environment is consistent algae indicates that the Lower Miocene grainstone
with high water energy (Bosence, 1991; Basso, was deposited in warm tropical to subtropical
1998; Nebelsick et al., 2000). Agitation in the shoal waters (Bosence, 1983a, 1983b; Braga and Agu-
environment, resulted different taphonomic fea- irre, 2001; Brandano et al., 2005; Roozpeykar et
tures such as high fragmentation, disarticulation, al., 2019a). Moreover, tropical conditions can be
and abrasion of several algae (Nebelsick et al., inferred owing to the presence of skeletal grains
2000; Nebelsick and Bassi, 2000; Roozpeykar et al., of corals and larger benthic foraminifera such as
2019a, 2019b). The identified algae (Table 1 and miliolids, Amphistegina, and Nephrolepidina in the
Figures 5–8) and the presence of larger benthic studied grainstone facies (Pomar et al., 2004; Bran-
foraminifera point to a well-illuminated euphotic dano et al., 2009; Roozpeykar et al., 2019a, 2019b).
CONCLUSIONS / CONTRIBUTIONS OF AUTHORS
http://dx.doi.org/10.18268/BSGM2022v74n2a020122
Figure 8 Identified coralline red algae in the grainstone facies. (A) Fragment of a fruticose thallus of Lithothamnion sp. (B) Fragment of
Lithothamnion sp. (encrusting growth form). (C) Melobesioid algae with a fruticose growth form.
Braga, J.C., Aguirre, J., 2004, Coralline algae of Menorca (Spain): environmental and
REFERENCES
indicate Pleistocene evolution from paleoclimatic implications: Palaeogeography
deep, open platform to outer barrier Palaeoclimatology Palaeoecology, 226
reef environments in the northern Great (3), 307–323. https://doi.org/10.1016/j.
Barrier Reef margin: Coral Reefs, 23, palaeo.2005.04.034
547–558. https://doi.org/10.1007/ Coletti, G., Basso, D., Corselli, C., 2018,
s00338-004-0414-x Coralline algae as depth indicators in the
Braga, J.C., Bassi, D., Piller, W., 2010, Sommiéres Basin (early Miocene, Southern
Palaeoenviromental significance of France): Geobios, 51, 15–30. https://doi.
Oligocene–Miocene coralline red algae – org/10.1016/j.geobios.2017.12.002
a review, in Mutti, M., Piller, W., Betzler, Daneshian, J., Ramezani Dana, L., 2007,
C. (eds.), Oligocene-Miocene carbonate Early Miocene benthic foraminifera and
systems: International Association of biostratigraphy of the Qom Formation,
Sedimentologists, Special Publication, 42, Deh Namak, central Iran: Journal of Asian
165–182. Earth Sciences, 29, 844–858. https://doi.
Braga, J.C., Martín, J., 1988, Neogene coralline-algal org/10.1016/j.jseaes.2006.06.003
growth-forms and their palaeoenvironments Dunham, R.J., 1962, Classification of carbonate
in the Almanzora River Valley (Almeria, SE rocks according to depositional textures, in
Spain): Palaeogeography Palaeoclimatology Ham, W.E. (ed.), Classification of carbonate
Palaeoecology, 67(3), 285–303. https://doi. rocks: AAPG, 108–121.
org/10.1016/0031-0182(88)90157-5 Erlich, R.N., Barrett, S.F., Bai, J.G., 1990,
Brandano, M., Piller, W.E., 2010, Coralline algae, Seismic and geologic characteristics of
oysters and echinoids-a liaison in rhodolith drowning events on carbonate platforms:
formation from the Burdigalian of the Latium- AAPG Bulletin, 74, 1523–1537. https://
Abruzzi Platform (Italy): International doi.org/10.1306/44b4b068-170a-11d7-
Association of Sedimentologists, Special 8645000102c1865d
Publication, 42, 149–164. https://doi. Erlich, R.N., Longo, A.P., Hyare, S., 1993, Response
org/10.1002/9781118398364.ch9 of carbonate platform margins to drowning:
Brandano, M., Ronca, S., 2014, Depositional evidence of environmental collapse, in
processes of the mixed carbonate–siliciclastic Louks, R.G., Sarg, J.F. (eds), Carbonate
India: Geoscience Frontiers, 4, 755–764. Rahiminejad, A.H., Nouradini, M., Yazdi, M.,
https://doi.org/10.1016/j.gsf.2013.01.010 2017, Palaeoenvironmental analysis of
Halfar, J., Mutti, M., 2005, Global dominance scleractinian reef corals from the Oligo-
of coralline red algal facies: a response to Miocene Qom Formation in the Vartun
Miocene oceanographic events: Geology, section (northeastern Esfahan, central Iran):
33, 481–484. https://doi.org/10.1130/ Historical Biology, 29(3), 384–394. https://
g21462.1 doi.org/10.1080/08912963.2016.1167201
Moosavizadeh, S.M.A., Zand-Moghadam, Rahiminejad, A.H., Yazdi, M., Ashouri, A.R.,
H., Rahiminejad, A.H., 2020, Kangazian, A., 2018, Siliciclastic input
Palaeoenvironmental reconstruction and sedimentation rate as controls on
and sequence stratigraphy of the Lower paleoecological distribution of Lower
Cretaceous deposits in the Zagros belt, Miocene benthic carbonate producers in
SW Iran: Boletín de la Sociedad Geológica a fan–delta: Zagros foreland basin, Iran:
Mexicana, 72 (2), A060919. https://doi. Historical Biology, 30 (5), 608–626. https://
org/10.18268/bsgm2020v72n2a060919 doi.org/10.1080/08912963.2017.1312360
Moradi, S., 2012, Study of Microfacies, Rahiminejad, A.H., Yazdi, M., Bahrami, A.,
depositional environment and diagenesis of 2020, Palaeoenvironments and taphonomy
the Qom Formation in Abgarm anticline, SE of clypeasteroids in Miocene carbonates
Chahriseh, NE Isfahan: Iran, University of of the Esfahan–Sirjan Basin, central Iran:
Isfahan, MSc dissertation. Facies, 66, 14. https://doi.org/10.1007/
Nebelsick, J.H., Bassi, D., 2000, Diversity, growth s10347-020-00598-6
forms and taphonomy: key factors controlling Rahiminejad, A.H., Zand-Moghadam, H.,
the fabric of coralline algae dominated shelf 2018, Synsedimentary formation of ooidal
carbonates: Geological Society, London, ironstone: An example from the Jurassic
Special Publications, 178, 89–107. https:// deposits of SE central Iran: Ore Geology
doi.org/10.1144/gsl.sp.2000.178.01.07 Reviews, 95, 238–257. https://doi.
Nebelsick, J.H., Bassi, D., Drobne, K., 2000, org/10.1016/j.oregeorev.2018.02.028
Microfacies analysis and interpretation of Rasser, M., Piller, W., 2004, Crustose algal
Lower Oligocene, Shallow-water carbonates frameworks from the Eocene Alpine foreland:
Miocene coralline red algae from the Qom Formation
Southeast Asia): Palaios, 30(1), 83–93. a case study from Devonian of Paraná Basin,
REFERENCES
https://doi.org/10.2110/palo.2013.055 Brazil: Lethaia, 51(1), 15–34. https://doi.
Roozpeykar, A., Maghfouri-Moghaddam, I., org/10.1111/let.12219
Yazdi, M., Yousefi-Yegane, B., 2019a, Seyrafian, A., Toraby, H., 2005, Petrofacies and
Paleontology and paleoecology of coralline sequence stratigraphy of the Qom Formation
algal assemblages from the Early–Middle (Late Oligocene- early Miocene?), north
Miocene deposits in NW of the Zagros of Nain, southern trend of central Iranian
basin, Iran: Carbonates and Evaporites, basin: Carbonates and Evaporites, 20, 82–90.
34, 1595–1618. https://doi.org/10.1007/ https://doi.org/10.1007/bf03175451
s13146-019-00509-z Stöcklin, J., Setudehina, A., 1991, Stratigraphic
Roozpeykar, A., Maghfouri-Moghaddam, I., lexicon of Iran: Geological Survey of Iran
Yazdi, M., Yousefi-Yegane, B., 2019b, Facies Report, 18, 376 p.
and paleoenvironmental reconstruction of Vescogni, A., Bosellini, F.R., Cipriani, A., Gürler,
Early- Middle Miocene deposits in the north- G., Ilgar, A., Paganelli, E., 2014, The
west of the Zagros Basin, Iran: Geologica Dağpazarı carbonate platform (Mut Basin,
Carpathica, 70(1), 75–87. https://doi. Southern Turkey): facies and environmental
org/10.2478/geoca-2019-0005 reconstruction of a coral reef system during
Sadeghi, R., Vaziri-Moghaddam, H., Taheri, the Middle Miocene Climatic Optimum:
A., 2011, Microfacies and sedimentary Palaeogeography Palaeoclimatology
environment of the Oligocene sequence Palaeoecology, 410, 213–232. https://doi.
(Asmari Formation) in Fars sub-basin, org/10.1016/j.palaeo.2014.05.040
Zagros Mountains, southwest Iran: Facies, Vinn, O., Wilson, M.A., 2013, An event bed with
57, 431–446. https://doi.org/10.1007/ abundant Skolithos burrows from the late
s10347-010-0245-x Pridoli (Silurian) of Saaremaa (Estonia):
Sarkar, S., 2017, Ecology of coralline red algae and Carnets de Géologie [Notebooks on
their fossil evidences from India: Thalassas, Geology], Brest, Letter, 83–87. https://doi.
33, 15–28. org/10.4267/2042/49316
Sarkar, S., Ghosh, A. K., 2015, Evaluation of Woelkerling, W.J., Irvine, L.M., Harvey, A.S., 1993,
coralline algal diversity from the Serravallian Growth-forms in Non-geniculate Coralline
carbonate sediments of Little Andaman Red Algae (Corallinales, Rhodophyta):
Zabihi Zoeram, F., Vahidinia, M., Sadeghi, A., and Mines and Geological Survey of Iran.
REFERENCES