Journal of Threatened Taxa |
www.threatenedtaxa.org | 26 April 2023 | 15(4): 23101–23113
ISSN 0974-7907 (Online) | ISSN 0974-7893
(Print)
https://doi.org/10.11609/jott.7813.15.4.23101-23113
#7813 | Received 31 December 2021 | Final
received 24 March 2023 | Finally accepted 02 April 2023
Recent Foraminifera from the
coast of Mumbai, India: distribution and ecology
Ganapati Ramesh Naik 1,
Manisha Nitin Kulkarni 2 & Madhavi Manohar Indap 3
1,3 Department of Zoology, Central
Research Laboratory, D.G. Ruparel College of Arts, Science & Commerce, Senapati Bapat Marg, Mahim, Mumbai,
Maharashtra 400016, India.
2 Department of Zoology, The
Institute of Science, 15, Madam Cama Road, Mumbai, Maharashtra 400032, India.
1 gnsrnaik@gmail.com, 2 harmonium.mnk@gmail.com,
3 madhaviindap@yahoo.com (corresponding author)
Editor: Rajashekhar K. Patil, Mangalore University,
Mangalore, India. Date of
publication: 26 April 2023 (online & print)
Citation: Naik, G.R., M.N. Kulkarni & M.M. Indap (2023). Recent Foraminifera from the coast of
Mumbai, India: distribution and ecology. Journal of Threatened Taxa 15(4): 23101–23113. https://doi.org/10.11609/jott.7813.15.4.23101-23113
Copyright: © Naik et al. 2023. Creative Commons Attribution 4.0 International License. JoTT allows unrestricted use, reproduction,
and distribution of this article in any medium by providing adequate credit to
the author(s) and the source of publication.
Funding: There is no Government funding.
Partially funded by Fine Envirotech Engineers, Mumbai.
Competing interests: The authors declare no competing
interests.
Author details: Mr.
Ganapati Ramesh Naik, PhD research
scholar at D G Ruparel College’s Department of Zoology, Central Research
Laboratory. Has spent the last six years working in the subject of marine
ecology. Dr. Manisha Nitin Kulkarni is currently a professor in the
Department of Zoology at The Institute of Science in Mumbai. Her
scientific interests include biodiversity and endocrinology. Dr.
Madhavi Manohar Indap is an emeritus professor. Adjunct faculty
at D G Ruparel College’s Central Research Laboratory in Mumbai. Her areas of
interest in study include biodiversity, ecology, and
marine biotechnology.
Author contributions: Madhavi Indap (MI) had conceptualized the
study, directed and finalized the manuscript. Ganapati Naik (GN) collated in
the information, evaluated the data and wrote the manuscript.
Manisha Kulkarni (MK) had supervised the manuscript.
Acknowledgements: We are thankful to National
Centre for Nano-sciences and Nanotechnology, University of Mumbai (NCNNUM) for
providing us the facility of scanning electron microscopy (SEM) for our work.
We are grateful to Fine Envirotech Engineers, Mumbai for providing financial
help to carry out this work.
Abstract: Foraminifera have been used in
biostratigraphy and paleoenvironmental research. They are useful environmental
indicators for monitoring the marine environment. Intertidal sediment samples
were analysed for their diversity in relation to physicochemical parameters and
sediment characteristics along the Mumbai coast of India. Thirty-five species
were found, divided into five orders and 18 families. The orders Rotaliida and
Miliolida were identified to be dominant. Foraminifera were observed to be
inversely related to sand particle size in relation to sediment and
physicochemical parameters of water. Canonical correlation analysis explained
the relationship between species abundance and water physicochemical
parameters.
Keywords: Abundance, anthropological
activities, environmental indicators, foram, grain size, marine coastal area,
physicochemical factors, Protista
Abbreviations: CCA—Canonical correlation
analysis | DO—Dissolved oxygen | MON—Monsoon | MPCB—Maharashtra Pollution
Control Board | OC—Organic carbon | OM—Organic matter | POM—Post-monsoon |
PRM—Pre-monsoon | TFN—Total foraminifera number | WNT—Winter.
Introduction
Mumbai, the state
capital of Maharashtra, has a population of about 22 million people. It is also
the largest and busiest port on India’s west coast. Intertidal zone of Mumbai
represents the peak of adaptability by most types of marine life to harsh
environmental circumstances such as wave action, desiccation and other
associated aspects generated by the tides of the sea (Kameswara & Srinath
2002). Among marine microorganisms, foraminifera are exceptionally varied and
widely spread (Cushman et al. 1928). They are distinguished as protists by
having an external test and streaming granular ectoplasm. Their tests are
composed of calcium carbonate or agglutinated sediments, which are well
preserved after death (Vidya & Patil 2014). They are considered good ecological
indicators for detection and monitoring of coastal pollution (Pravasini &
Patra 2012). According to Fabrizio et al. (2013), Ammonia tepida has a
high resistance to environmental stress while Ammonia parkinsoniana is
sensitive to pollution. These are the most widely used fossil species for
biostratigraphy, sediment correlation and palaeoenvironmental research (Murray
2006) and their usage as bio-indicators in offshore oil drilling operations is
well documented (Mariéva et al. 2010). Abninath & Biswas (1954), Devi &
Rajashekhar (2009), and Subhadra & Patil (2012) conducted intertidal
studies of foraminifera from the Mumbai coast on diversity studies in the
intertidal region. Coastal water is vulnerable to contamination since 38% of
the world’s population lives within 100 kilometres of the coast (Pravasini
& Patra 2012). Coastal pollution is caused by point and non-point
wastewater sources from cities, which include sewage water, waste from industry
and harbours, beach tourism and fishing crafts activities. Pollution has a
negative impact on organisations at all levels, from the organism to the
community and the environment (Francisco et al. 2011).
The current study
was undertaken to document the Foraminifera at several sites along the Mumbai
coast. The objective was to determine the relationship between foram abundance
and various physicochemical factors, as well as anthropological activities.
This information will aid in the creation of a database of foraminifera along
Mumbai’s coastline and contribute to understanding the effects of natural and
anthropogenic events on Foraminifera.
Study Area
Mumbai is located
at 19.0760° N & 72.8777° E, with an overall coast length of 149 km. Four
coastal locations with distinct ecology were chosen for sampling. These sites
range from north to south along the Mumbai shoreline (Figure 1). Gorai beach
(M1) is located in Mumbai’s northwestern outskirts. It is regarded as one of
Mumbai’s cleanest beaches. Juhu beach (M2) has a five-kilometre coastline.
Dadar beach (M3) is situated on the south-west side of Mahim Island. Girgaon
beach (M4) is located on Mumbai Island’s south-west coast. M2, M3, and M4 are
well-known tourist attractions. Mumbai’s water quality is deteriorating as a
result of pollutants from wastewater treatment facilities, sewage discharges,
and discharges from point and non-point sources in the creek and along the
shore (Ritesh et al. 2015).
Material and Methods
Sediment samples
were collected in two phases: September 2013–August 2014 and December
2016–November 2017, from four stations: M1, M2, M3, and M4. The sampling was
divided into four seasons: pre-monsoon (March–May), monsoon (June–August),
post-monsoon (September–November), and winter (December–February).
Using a scientific
spatula, the upper one cm layer of sand sediment was collected in duplicates
between the intertidal zone during low tide. Forams were stained using Rose
Bengal solution and stored in 70% isopropyl alcohol (Walton et al. 1952). The
materials were washed through a 63 µm sieve and oven-dried at 60°C for
analysis. A stereo microscope was used to examine one gram of sand from
each station. The total number of specimens (live + dead) was used to calculate
abundance. Foram tests were hand-picked and put on micro-paleontological slides
using a foram sorting brush. ‘JEOL JSM - 5800VS’ scanning electron microscope
(SEM) was used to image selected specimens. The Loeblich & Tappan
(1988) classification system and the e-site “World Foraminifera Database”
(Hayward et al. 2022) were used for taxonomic analysis.
Temperature, pH,
salinity, dissolved oxygen (DO), phosphates and nitrates were chosen as water
physicochemical parameters. A digital thermometer was used to record the
temperature of the water at sample sites. pH, salinity and DO were measured
with a “Thermo Scientific Eutech PCD-650 multi-parameter metre.” Nutrients
nitrate and phosphate were estimated using standard methods given in the APHA
manual (Lenore et al. 1999).
Another batch of
sand sediment was collected for measurement of organic carbon by titration with
ammonium ferrous sulphate using the Walkley-Black technique with suitable
modification (Syed et al. 2011). To determine the texture of sand sediment,
samples were sieved through multiple mesh sizes. The soil textural triangle
approach (Derek et al. 2015) was used to determine their type. Past 3 v4.03
software was used to calculate diversity indices including the Shannon index,
Simpson index, Evenness, Margalef index, canonical correlation, and Q-mode
cluster.
ResultS and Discussion
Foraminifera Assemblage & Physicochemical
Parameters
The current study
revealed the existence of 35 species from four orders, 18 families and
21 genera (Table 1). These 35 species were divided into 33 benthic and two
planktonic species. M1, M2, M3, and M4 stations revealed the presence of 34,
32, 33, and 22 species, respectively. Order Rotaliida was dominant with 19
species, followed by order Miliolida, which had 11 species. The dominant
species identified along Mumbai’s shore were Nonion scaphum (17.8%), Ammonia
beccarii (15.7%), A. dentata (12%), Elphidium hispidulum
(8.9%), and Bolivina striatula (5.7%). Table 2 has a Foraminifera
checklist. Images 1 (1–20) and 2 (1–19) displays SEM images that illustrate the
morphological trait of species.
The total Foraminifera
number (TFN) is the total number of individuals found in one gram of
sediment. TFN values in samples ranged from 590 at M2 to 178 at M4 per gram.
Northern Mumbai stations (M1, M2) showed greater values, whereas southern
Mumbai stations recorded lesser values (M3, M4).
Shannon index (H)
represented both species abundance and evenness in areas ranging from 2.06 (M4)
to 2.77 (M2). Simpson index of dominance (D) revealed the dominance of
cosmopolitan species with values 0.08 (M2) to 0.21 (M4). Equitability index
revealed species evenness (e^H/S) with values ranging from 0.41 (M3) to 0.67
(M4). The Margalef index of species richness ranged from 2.09 (M4) to 5.04
(M1), and is directly related to taxonomic numbers 12 (M4) and 32 (M1). Table 3
presents the diversity indices.
The water
parameters including pH, temperature, salinity, dissolved oxygen, phosphate,
and nitrate were considered for study of various seasons including,
pre-monsoon, monsoon, post-monsoon, and winter, which are represented in Table
4.
The pH ranged from
6.54 at M2 during post-monsoon to 7.89 at M4 during monsoon. Water temperatures
in the intertidal zone ranged from 25°C reflecting monsoon at M4 to 29°C
representing pre-monsoon at M1. Salinity at all sites varied with the seasons,
ranging from 17 during the monsoon at M1 to 41 during the pre-monsoon at M2.
Dissolved oxygen,
phosphate and nitrate showed variations in its concentrations. DO levels were
highest during the pre-monsoon (7.4 mg/l) and lowest during the winter
(3.1 mg/l) at M1. Similarly, in monsoon, M4 station had the lowest phosphate
and nitrate levels, viz., 0.14 mg/l and 0.1 mg/l and M3 in winter revealed the
greatest phosphate and nitrate ranges 0.56mg/l to 1.5mg/l, respectively.
The sediment type
study revealed that silt type occurred at the M1 and M2, loamy sand
at the M3 and sandy loam at the M4. The organic carbon percentage of sediment
varied between stations, ranging from 0.28% to 0.37% (Table 4).
Pearson Correlation & Canonical Correlation
Analysis (CCA)
For the water parameters
and diversity indices, a Pearson correlation matrix was calculated (Table
5). The pH and dissolved oxygen correlated positively with species evenness but
negatively with the other indices. Temperature correlated positively with the
number of taxa, the H index and the Margalef index. Salinity only correlated
positively with species dominance. Phosphate and nitrate had a significant
negative correlation with species evenness.
CCA defined a
relationship between species, stations and environmental parameters (Figure 2).
For this analysis, species having a total population more than 1% was
chosen, which included population of 18 species. Phosphate and
dissolved oxygen defined axis one, whereas nitrate, pH, salinity, and
temperature defined axis two. According to CCA analysis nitrate, pH and
salinity correlated positively, but temperature correlated negatively with all
other physicochemical parameters. All of the water parameters were found
to have a significant correlation with 12 species.
Ammonia beccarii, E.
repandus, A. dentata, and S. raphana were
abundant at three sample stations displayed in the top-right quadrant of the
graph. T. oblonga, A. intricata, T. tricarinata,
and E. hispidulum peaked at five stations in the bottom right
quadrant of the graph. Q. vulgaris, U. senticosa, N.
scaphum, and B. pseudoplicata showed the highest abundance at five stations represented at
top-left quadrant of graph and species B. marginata, R. globularis,
B. striatula, C. lobatulus, Q. tropicalis,
and E. advenum were most abundant at three stations represented
at bottom-left quadrant of graph.
A. beccarii
and A. dentata are mainly found in waters with high nitrate
levels. N. scaphum was well associated with ambient temperature
and phosphate concentration. B. striatula, C. lobatulus
and Q. tropicalis held the average positions for all
parameters. E. hispidulum and T. tricarinata were
significantly correlating with DO, pH, and salinity.
Species-ecological Relationship
This research
attempted to investigate the relation of foraminifera to intertidal benthic
ecology at different stations. Data from physicochemical parameters were
correlated with dominant species using specific indices.
At M1 TFN ranged from 533 to 450 individuals
per gram, it was represented by 34 species. N. scaphum (28.33%), A. dentata
(12.3%), E. hispidulum (8%) and A. beccarii
(7.64%) were dominant species representing the area. According to Kumar &
Manivannan (2001) N. scaphum has shown positive
correlation to an increase in temperature and DO, our data support this
statement. During the winter, the Simpson’s index 0.14 is correlating with
nitrate value. There is cumulative impact of nitrate and temperature with
bleaching response on foraminifera (Martina et al. 2017), allowing
only tolerant species to thrive. Thirty-one species have been identified
at M2, with a maximum foraminifera test count of 590 in pre-monsoon. Here major
taxa were again N. scaphum (21%), A. dentata
(10.82%), and A. beccarii (10.59%). Phosphate has long been
recognized as a calcite formation inhibitor, adsorbing onto the calcite surface
and inhibiting active crystal growth sites (Aldridge et al. 2011), which might
account for lower test numbers than M1. After A. beccarii,
the dominant species was B. striatula (8.12%). Lagena, Fissurina,
Bolivina, Bulimina, and Uvigerina species are found in
finer sediments and exist in the shelf to slope area, according to Rajiv et al.
(1986); however their prevalence in the study area may be due to wave action.
M3 receives water runoff from the Mithi River and had low salinity during the
monsoon due to monsoon water, in addition to large amount of sewage and
industrial garbage from the Mithi (Jayasiri et al. 2014). At the M3, 33
distinct taxa were present. A. beccarii (24.18%), A. dentata
(15.2%), and E. hispidulum (12.21%) dominated the station. M4 had
taxa count 20 with a maximum of 198 individuals. The dominant species
representing the area were A. beccarii (32.67%), T. tricarinata
(15.02%), and E. hispidulum (11.55%).
The distribution of
benthic Foraminifera is influenced by organic carbon (OC) and sediment type
(Elakkiya & Manivannan 2013). Benthic foram have been shown to be closely
associated with variations in percent gravel, organic carbon flux, temperature
and salinity (Alexandra et al. 2007). The sediment at stations M1 and M2 was
silt type, with 0.34% and 0.28% organic carbon, respectively. At M1 Margalef
index of 5.04 and at M2 Shannon value of 2.77 were both positively
correlated with sediment type, as sand mixed with shelly fragments and silt or
clay support the richest standing crop of foraminifera (Chaturvedi et al.
2000). Station M3 had loamy sand with the highest organic carbon content of
0.37% of all stations. Water discharge from Mahim Creek has the highest
percentage of organic carbon, as the creek is the largest sink for the most of
waste created by residential complexes and small-scale industry (Singare et al.
2015). Station M4 is associated with 0.31% organic carbon with sediment
particle size larger than other stations. According to Elena et al. (2019)
stations exposed to the open sea and intensified currents were defined by
coarser sediments. As M4 had sandy loam type of sediment
suggesting good wave action due to its association with open sea. The
moderate value of OC at this station is associated with sediment type, since in
coarse-grained sand, interstitial water may travel easily through pore spaces,
resulting in less organic particle settling (Hiroshi 1994).
A. beccarii
and A. dentata correlated negatively with DO values from all
stations, making them adaptable to anoxic conditions (Fatin et al. 2012;
Sundara et al. 2016). B. striatula which thrived well in low
oxygen stations (Abhijit & Nigam 2014) and was positively associated to
salinity since it is an opportunistic species that can thrive in both high and
low salinity conditions (Patricia et al. 2019). The dominance of Ammonia sp.
and Elphidium sp. in study area indicated that they are resistant to
decreased salinity, pH or a combination of the two factors (Laurie et al.
2018).
N. scaphum
adapted to environments characterized by high organic matter (OM) quality and
it indicates affinity for OM-rich sediments (Pierre et al. 2016), so its
distribution is well associated with M1 and M2 as compared to M4 which had more
coarse type of sediment. A. dentata and E. hispidulum
was abundant at M1, M2 and M3 as silt sand is preferred by the species over
coarse sandy sediment (Elakkiya & Manivannan 2013), with affinity for
larger amount of organic carbon values (Maria et al. 2012). However, based on
our understanding of above work on foraminifera, we may conclude that the
cosmopolitan species A. beccarii, A. dentata, B.
striatula, N. scaphum, and E. hispidulum
thrive well in Mumbai waters.
Hierarchical Cluster Analysis
Foraminifera species
were tested to a Bray-Curtis cluster analysis in relationship to stations
(Figure 3). It divided stations into three groups: Cluster A (M1 + M2), Cluster
B (Cluster A + M3), and Cluster C (Cluster B + M4).
Cluster A consists
of two stations (M1 + M2) that share 32 species. It had a similar type of
sediment, silt with physicochemical properties. CCA analysis showed these
stations near to one other on the middle and left sides of Axis one. The main
representatives of this cluster were N. scaphum (21–28.3%), A.
beccarii (7.6–10.5%), A. dentata (10.8–12.3%), B. striatula
(6.6–8.1%), B. pseudoplicata (5.5–5.6%), C. lobatulus
(4.7–5.5%), Q. tropicalis (3.5–6.4%), E. hispidulum
(6.5–8%), U. senticosa (2.9–3.7%), T. tricarinata (1.8–3.5%)
and B. marginata (2.8–3.1%). Species like N. scaphum,
A. dentata, and B. striatula have more affinity for
fine sediment like silt than coarse type of sediment.
Cluster B comprised
of three stations (Cluster A + M3) with 31 species in common. In this cluster
M3 is having more similarity with M2 than M1. The cluster had silt and loamy
sand sediment which showed a little correlation with one another. The main
species represented by the cluster were N. scaphum (8.2–28.3%),
A. beccarii (7.6–24.1%), A. dentata (10.8–15.2%), E.
hispidulum (6–12.2%), T. tricarinata (1.8–6.2%), E.
repandus (0.9–3.3%), C. lobatulus (3.2–5.5%), B. striatula
(3.1–8.1%), and Q. tropicalis (3.2–6.4%).
Cluster C comprised
of all four stations (Cluster B + M4) that share 22 species in common. In this
cluster M4 had more similarity with M3 as compared with Cluster A. As M3 and M4
had loamy sand and sandy loam sediment, which had more similarity with each
other. Having a more coarse type of sediment was responsible for more resistant
taxa to sediment particle movements by wave action. The main species
represented by the cluster were A. beccarii (1.9–28.3%), T.
tricarinata (1.8–15%), E. hispidulum (6.5–11.5%), A.
dentata (8.5–15.2%), E. repandus (0.9–5.2%), E. advenum
(1.6–4.1%), T. oblonga (0.8–3.1%), and R. globularis
(1.1–2.3%).
Test Deformity
Environmental
stress induced by large fluctuations in environmental factors such as salinity,
DO, temperature, pH, sedimentation, pollution and hydrodynamics has been
connected to a significant percentage of abnormal tests in foraminiferal
assemblages (Rehab et al. 2011). Mumbai is India’s economic hub, and increased
urbanization and industrialization have resulted in an increase in marine
discharges to coastal areas (Jayasiri et al. 2014). According to Maharashtra
Pollution Control Board (MPCB) data on Maharashtra’s water quality condition,
water at stations Juhu (M2), Dadar (M3), and Girgaon (M4) had a bad water
quality index (MPCB 2013–14, 2016–17). In the present study Quinqueloculina
sp. (M3), Triloculina sp. (M3), Siphogenerina raphana (M2,
M3) and an Undetermined taxa showed the abnormal formation of shells.
These deformed tests have been shown in Image 2 (15–19).
Quinqueloculina sp. (M3)
showed reduced chambers, Triloculina sp. (M3) had twisted
chambers, Siphogenerina raphana (M2, M3) represented by enlarged
chambers and uneven costae lines, and the undetermined taxa had
unusually extended chambers. These abnormalities imply that environmental
conditions and industrialization have had a negative impact on foraminiferal
diversity. All of these abnormalities were associated predominantly with M3
station. According to studies conducted by Shamrao & Kadam (2003),
Jayasiri et al. (2014), and Ritesh et al. (2015), Dadar beach is extremely
contaminated owing to effluents carried in by the Mithi River, with low-energy
hydrodynamics generated by the lagoon region. According to MPCB publications
(MPCB 2013–14, 2016–17), the water quality index for M3 is also rated as bad to
very-bad. According to Suresh & Sonia (2012) morphological abnormalities
are induced by pollution, strongly in shallow waters than deep seas. According
to Jayaraju et al. (2008), heavy metal contamination has a greater
negative impact on foraminiferal test morphology than agricultural and
aquacultural wastes. From these damaged shells it may be concluded that they
act as a sensitive taxon to environmental and anthropogenic conditions.
Conclusion
The present study
revealed diversity and distribution of Foraminifera along Mumbai coast with
presence of 35 species belonging to four orders, 18 families, and 21 genera.
The orders Rotaliida and Miliolida dominated the taxa. A. beccarii,
N. scaphum, A. dentata, and E. hispidulum
were the most opportunistic species present at all stations. Due to
similarities in sediment and species distribution, CCA and Bray-Curtis
similarity analysis revealed that M1-M2 and M3-M4 were more associated with
each other. N. scaphum served as sensitive taxa by showing
affinity for oxygen and finer sediment type. A. beccarii and E.
hispidulum acted as stress tolerant taxa flourishing well in fine as
well as coarse sediment type. The presence of B. striatula
indicated the hypoxic condition of water and sediment during winter season. The
study found that finer to medium grain sand was associated with more species
than coarse sand. Organic carbon concentrations correlated directly with fine
sediment type and stations with low-energy hydrodynamic circumstances (M1, M3),
allowing more organic carbon to trap between sand particles. The presence of
deformed tests suggested that Mumbai’s coastal water had physicochemical
parameter fluctuations and received contaminated water from industrial areas.
It symbolized the potential use of foraminifera in understanding the effects of
urbanization and industrialization on coastal water. This creates a great need
to construct foraminifera study models to comprehend long-term consequences of
changing environmental and anthropogenic activities along urban coasts, since
we cannot halt industrialization, but such research will assist to limit the
impact of pollution on the marine environment.
Table 1. Foraminiferal taxa composition along with the
stations of Mumbai coast.
|
Order |
Family |
Genus |
Species |
1 |
Rotaliida |
Nonionidae |
Nonion |
Nonion scaphum |
2 |
Ammoniidae |
Ammonia |
Ammonia beccarii |
|
3 |
Ammonia dentata |
|||
4 |
Bolivinitidae |
Bolivina |
Bolivina striatula |
|
5 |
Bolivina pseudoplicata |
|||
6 |
Siphogenerinoididae |
Spiroloxostoma |
Spiroloxostoma glabra |
|
7 |
Siphogenerina |
Siphogenerina raphana |
||
8 |
Siphogenerina sp. |
|||
9 |
Elphidiidae |
Elphidium |
Elphidium hispidulum |
|
10 |
Elphidium advenum |
|||
11 |
Elphidium sp. |
|||
12 |
Rosalinidae |
Rosalina |
Rosalina globularis |
|
13 |
Eponididae |
Eponides |
Eponides repandus |
|
14 |
Cibicididae |
Cibicides |
Cibicides lobatulus |
|
15 |
Discorbinellidae |
Discorbinella |
Discorbinella sp. |
|
16 |
Buliminidae |
Bulimina |
Bulimina marginata |
|
17 |
Uvigerinidae |
Uvigerina |
Uvigerina senticosa |
|
18 |
Globigerinidae |
Globigerina |
Globigerina bulloides |
|
19 |
Globigerinoides |
Globigerinoides sp. |
||
20 |
Miliolida |
Hauerinidae |
Quinqueloculina |
Quinqueloculina tropicalis |
21 |
Quinqueloculina porterensis |
|||
22 |
Quinqueloculina vulgaris |
|||
23 |
Quinqueloculina polygona |
|||
24 |
Quinqueloculina agglutinans |
|||
25 |
Triloculina |
Triloculina tricarinata |
||
26 |
Triloculina oblonga |
|||
27 |
Spiroloculinidae |
Spiroloculina |
Spiroloculina antillarum |
|
28 |
Spiroloculina communis |
|||
29 |
Cribrolinoididae |
Adelosina |
Adelosina intricata |
|
30 |
Cornuspiridae |
Cornuspira |
Cornuspira involvens |
|
31 |
Nodosariida |
Lagenidae |
Lagena |
Lagena vulgaris |
32 |
Lagena sulcata |
|||
33 |
Lagena laevis |
|||
34 |
Polymorphinida |
Ellipsolagenidae |
Fissurina |
Fissurina cucullata |
35 |
Fissurina sp. |
Table 2. Distribution of Foraminifera species along
four stations of Mumbai coast.
|
Species |
M1 |
M2 |
M3 |
M4 |
1 |
Nonion scaphum |
+ |
+ |
+ |
+ |
2 |
Ammonia beccarii |
+ |
+ |
+ |
+ |
3 |
Ammonia dentata |
+ |
+ |
+ |
+ |
4 |
Bolivina striatula |
+ |
+ |
+ |
+ |
5 |
Bolivina pseudoplicata |
+ |
+ |
+ |
+ |
6 |
Spiroloxostoma glabra |
+ |
+ |
+ |
- |
7 |
Siphogenerina raphana |
+ |
+ |
+ |
+ |
8 |
Siphogenerina sp. |
+ |
+ |
+ |
- |
9 |
Elphidium hispidulum |
+ |
+ |
+ |
+ |
10 |
Elphidium advenum |
+ |
+ |
+ |
+ |
11 |
Elphidium sp. |
+ |
- |
+ |
+ |
12 |
Rosalina globularis |
+ |
+ |
+ |
+ |
13 |
Eponides repandus |
+ |
+ |
+ |
+ |
14 |
Cibicides lobatulus |
+ |
+ |
+ |
+ |
15 |
Discorbinella sp. |
- |
- |
+ |
- |
16 |
Bulimina marginata |
+ |
+ |
+ |
+ |
17 |
Uvigerina senticosa |
+ |
+ |
+ |
+ |
18 |
Globigerina bulloides |
+ |
+ |
+ |
- |
19 |
Globigerinoides sp. |
+ |
+ |
+ |
- |
20 |
Quinqueloculina tropicalis |
+ |
+ |
+ |
+ |
21 |
Quinqueloculina porterensis |
+ |
+ |
+ |
- |
22 |
Quinqueloculina vulgaris |
+ |
+ |
+ |
+ |
23 |
Quinqueloculina polygona |
+ |
+ |
+ |
+ |
24 |
Quinqueloculina agglutinans |
+ |
- |
- |
- |
25 |
Triloculina tricarinata |
+ |
+ |
+ |
+ |
26 |
Triloculina oblonga |
+ |
+ |
+ |
+ |
27 |
Spiroloculina antillarum |
+ |
+ |
+ |
+ |
28 |
Spiroloculina communis |
+ |
+ |
+ |
+ |
29 |
Adelosina intricata |
+ |
+ |
+ |
+ |
30 |
Cornuspira involvens |
+ |
+ |
+ |
- |
31 |
Lagena vulgaris |
+ |
+ |
+ |
- |
32 |
Lagena sulcata |
+ |
+ |
+ |
- |
33 |
Lagena laevis |
+ |
+ |
- |
- |
34 |
Fissurina cucullata |
+ |
+ |
+ |
- |
35 |
Fissurina sp. |
+ |
+ |
+ |
- |
Table 3. Biodiversity indices of Foraminifera for
Mumbai coast.
Station |
Season |
Taxa |
Individuals |
Dominance |
Shannon |
Evenness |
Margalef |
M1 |
Pre-monsoon |
32 |
467 |
0.1249 |
2.646 |
0.4407 |
5.044 |
Monsoon |
28 |
533 |
0.1224 |
2.529 |
0.4479 |
4.3 |
|
Post-monsoon |
29 |
476 |
0.1203 |
2.585 |
0.4575 |
4.541 |
|
Winter |
28 |
450 |
0.1474 |
2.525 |
0.446 |
4.42 |
|
M2 |
Pre-monsoon |
29 |
590 |
0.1039 |
2.671 |
0.4983 |
4.389 |
Monsoon |
27 |
431 |
0.087 |
2.776 |
0.5945 |
4.286 |
|
Post-monsoon |
28 |
414 |
0.08698 |
2.757 |
0.5625 |
4.481 |
|
Winter |
27 |
486 |
0.1057 |
2.625 |
0.5113 |
4.203 |
|
M3 |
Pre-monsoon |
27 |
363 |
0.1259 |
2.528 |
0.4638 |
4.411 |
Monsoon |
29 |
385 |
0.1069 |
2.681 |
0.5035 |
4.703 |
|
Post-monsoon |
26 |
328 |
0.09856 |
2.644 |
0.5411 |
4.316 |
|
Winter |
29 |
389 |
0.1413 |
2.484 |
0.4132 |
4.695 |
|
M4 |
Pre-monsoon |
19 |
193 |
0.1416 |
2.317 |
0.5339 |
3.42 |
Monsoon |
12 |
192 |
0.1593 |
2.086 |
0.6711 |
2.092 |
|
Post-monsoon |
17 |
178 |
0.2122 |
2.064 |
0.4632 |
3.088 |
|
Winter |
20 |
198 |
0.1662 |
2.297 |
0.4971 |
3.593 |
Table 4. Physico-chemical parameters of water, organic
carbon, and sediment type from sampling stations.
Station |
Season |
pH |
Temperature (°C) |
Salinity (‰) |
Dissolved oxygen (mg/L) |
Phosphate (mg/L) |
Nitrate (mg/L) |
Organic carbon % |
Sediment type |
M1 |
Pre-monsoon |
7.52 |
29 |
30 |
7.4 |
0.2181 |
0.2 |
0.34 |
Silt |
Monsoon |
7.61 |
28 |
17 |
7.2 |
0.327 |
0.5 |
|||
Post-monsoon |
7.33 |
28 |
35 |
6.2 |
0.349 |
0.44 |
|||
Winter |
7.11 |
27 |
38 |
3.1 |
0.315 |
0.648 |
|||
M2 |
Pre-monsoon |
7.65 |
27 |
41 |
6.04 |
0.1455 |
0.95 |
0.28 |
Silt |
Monsoon |
7.6 |
27 |
32 |
7.1 |
0.269 |
0.513 |
|||
Post-monsoon |
6.54 |
28 |
37 |
6.4 |
0.328 |
0.465 |
|||
Winter |
7.42 |
28 |
38 |
3.45 |
0.413 |
0.782 |
|||
M3 |
Pre-monsoon |
7.43 |
28 |
38 |
5.8 |
0.264 |
0.65 |
0.37 |
loamy sand |
Monsoon |
7.06 |
27 |
25 |
6.7 |
0.261 |
0.38 |
|||
Post-monsoon |
7.81 |
27 |
36 |
6.1 |
0.352 |
0.425 |
|||
Winter |
7.39 |
28 |
38 |
3.42 |
0.563 |
1.5 |
|||
M4 |
Pre-monsoon |
7.09 |
29 |
39 |
6.1 |
0.214 |
0.687 |
0.31 |
Sandy loam |
Monsoon |
7.89 |
25 |
29 |
7.4 |
0.1454 |
0.1 |
|||
Post-monsoon |
7.05 |
27 |
37 |
6.7 |
0.361 |
0.456 |
|||
Winter |
7.45 |
27 |
39 |
4.6 |
0.289 |
0.663 |
Table 5. Pearson correlation analysis for diversity
indices and physico-chemical parameters of water.
|
pH |
Temperature |
Salinity |
Dissolved oxygen |
Phosphate |
Nitrate |
Taxa |
Individuals |
Dominance |
Shannon |
Evenness |
Margalef |
pH |
|
|
|
|
|
|
|
|
|
|
|
|
Temperature |
-0.3695 |
|
|
|
|
|
|
|
|
|
|
|
Salinity |
-0.2218 |
0.092786 |
|
|
|
|
|
|
|
|
|
|
Dissolved oxygen |
0.16147 |
-0.10486 |
-0.559 |
|
|
|
|
|
|
|
|
|
Phosphate |
-0.2266 |
0.27571 |
0.1359 |
-0.58298 |
|
|
|
|
|
|
|
|
Nitrate |
-0.0683 |
0.26441 |
0.4791 |
-0.70243 |
0.57205 |
|
|
|
|
|
|
|
Taxa |
-0.127 |
0.53909 |
-0.093 |
-0.17265 |
0.27933 |
0.2728 |
|
|
|
|
|
|
Individuals |
0.08318 |
0.29869 |
-0.193 |
-0.093673 |
0.083084 |
0.2117 |
0.85011 |
|
|
|
|
|
Dominance |
-0.0449 |
-0.22792 |
0.1315 |
-0.10616 |
0.057666 |
-0.012 |
-0.6639 |
-0.663 |
|
|
|
|
Shannon |
-0.0992 |
0.3675 |
-0.073 |
-0.028479 |
0.090162 |
0.1115 |
0.87788 |
0.78129 |
-0.9176 |
|
|
|
Evenness |
0.20239 |
-0.58162 |
-0.059 |
0.39673 |
-0.49099 |
-0.458 |
-0.5564 |
-0.3568 |
-0.2039 |
-0.1202 |
|
|
Margalef |
-0.1953 |
0.59841 |
-0.038 |
-0.19832 |
0.3278 |
0.2943 |
0.98356 |
0.74471 |
-0.614 |
0.85002 |
-0.6019 |
|
For Figures &
Images - - Click Here
References
Abhijit, M.
& R. Nigam (2014). Bathymetric preference of four major genera of rectilinear benthic
foraminifera within oxygen minimum zone in Arabian Sea off central west coast
of India. Journal of Earth System Science 123(3): 633–639. https://doi.org/10.1007/s12040-014-0419-y
Abninath,
C. & B. Biswas (1954). Recent Perforate Foraminifera from Juhu Beach, Bombay. The
Micropaleontology Project, Inc. 8(4): 30–32.
Aldridge,
D., C.J. Beer & D.A. Purdie (2011). Calcification in the planktonic foraminifera Globigerina
bulloides linked to phosphate concentrations in surface waters of the North
Atlantic Ocean. Biogeosciences Discussions 8: 6447–6472. https://doi.org/10.5194/bgd-8-6447-2011
Alexandra,
L.P., L. Sbaffi, V. Passlow & D.C. Collins (2007). Benthic
Foraminifera as Environmental Indicators in Torres Strait–Gulf of Papua. Mapping
the Seafloor for Habitat Characterization: Geological Association of Canada,
47: 329–347.
Chaturvedi,
S.K., R. Nigam & N. Khare (2000). Ecological Response of Foraminiferal Component in
the Sediments of Kharo Creek, Kachchh (Gujarat), West Coast of India. ONGC
Bulletin 37(2): 55–64.
Cushman, J.
(1928). Chapter 1:
The living animal. In: Foraminifea: Their Classification and Economic Use.
Sharon, Massachusetts, USA, 3 pp.
Derek,
G.G., T.P.A. Ferré, K.R. Thorp & A.K. Rice (2015). Hydrologic-Process-Based
Soil Texture Classifications for Improved Visualization of Landscape Function. PLoS
ONE10(6): e0131299. https://doi.org/10.1371/journal.pone.0131299
Devi, G.S.
& K.P. Rajashekhar (2009). Intertidal Foraminifera of Indian coast - a
scanning electron photomicrograph-illustrated catalogue. Journal of
Threatened Taxa 1(1): 17–36. https://doi.org/10.11609/JoTT.o1977.17-36
Elakkiya,
P. & V. Manivannan (2013). Recent benthic foraminifera from off the coast of
Arkattuthurai (near Nagapattinam), south east coast of India. Indian Journal
of Geo-marine Sciences 42(7): 877–887
Elena,
L.G.C., J.L. Clarke, C. Smeaton, K. Davidson & W.E.N. Austin (2019). Organic carbon
rich sediments: benthic foraminifera as bioindicators of depositional
environments. Biogeosciences 16: 4183–4199. https://doi.org/10.5194/bg-16-4183-2019
Fabrizio,
F., G. Margaritelli, F. Francescangeli, R. Rettori, E.A.D. Châtelet & R.
Coccioni (2013). Benthic foraminiferal assemblages and biotopes in a coastal lake: the
case study of lake Varano (southern Italy). ACTA Protozoologica 52:
147–160. https://doi.org/10.4467/16890027AP.13.0014.1111
Fatin,
I.M., K. Yahya, A. Talib & O. Ahmad (2012). Benthic
Foraminiferal Assemblages as Potential Ecological Proxies for Environmental
Monitoring in Coastal Water. 2nd International Conference on
Environment and BioScience 2012, IACSIT Press, Singapore, IPCBEE 44. https://doi.org/10.7763/IPCBEE.2012.V44.13
Francisco,
S.P.J.V. d. Brink & R.M. Mann (2011). Chapter 8: Impact of Pollutants on Coastal and Benthic
Marine Communities, pp 165., In. Ángel, B., M.J. Belzunce & J.M. Garmendia
(eds.). Ecological Impacts of Toxic Chemicals, Bentham Science
Publishers.
Hayward,
B., L.F. Coze, D. Vachard & O. Gross (2022). World foraminifera
Database. (http://www.marinespecies.org/foraminifera/)
Electronic version accessed 13 December 2022
Hiroshi, K.
(1994). Foraminiferal
microhabitats in four marine environments around Japan. Marine
Micropaleontology 24: 29–41. https://doi.org/10.1016/0377-8398(94)90009-4
Jayaraju,
N., B.C.S.R. Reddy & K.R. Reddy (2008). The response of benthic foraminifera to
various pollution sources: A study from Nellore Coast, East Coast of India. Environmental
Monitoring and Assessment 142: 319–323. https://doi.org/10.1007/s10661-007-9931-8
Jayasiri,
H.B., A. Vennila & C.S. Purushothaman (2014). Spatial and
temporal variability of metals in inter-tidal beach sediment of Mumbai, India. Environmental
Monitoring and Assessment 186: 1101–1111. https://doi.org/10.1007/s10661-013-3441-7
Kameswara,
K.R. & M. Srinath (2002). Foraminifera from beach sands along Saurashtra
coast, north-west India. Journal of the Marine Biological Association of
India 44(1&2): 22–36.
Kumar, V.
& V. Manivannan (2001). Benthic foraminiferal responses to bottom water characteristics in
the Palk Bay, off Rameswaram, southeast coast of India. Indian Journal of
Marine Sciences 30: 173–179.
Laurie,
M.C., H.L. Filipsson, Y. Nagai, S. Kawada, K. Ljung, E. Kritzberg & T.
Toyofuku (2018). Decalcification and survival of benthic foraminifera under the combined
impacts of varying pH and salinity. Marine Environmental Research 138:
36–45. https://doi.org/10.1016/j.marenvres.2018.03.015
Lenore, C.,
G. Arnold & E. Andrew (1999). Standard Methods for the Examination of Water and
Wastewater. American
Public Health Association, American Water Works Association and Water
Environment Federation, 20th edition, 1254 pp.
Loeblich,
A. & H. Tappan (1988). Foraminiferal genera and their
classification.Springer science, Business media, New York, 2031 pp.
MPCB
(2013–2014). Water Quality Status of Maharashtra, pp. 113–114. Maharashtra
Pollution Control Board
MPCB
(2016–2017). Water Quality Status of Maharashtra. Maharashtra Pollution Control
Board, 74 pp.
Maria,
C.M., L. Bergamin, M.G. Finoia, G. Pierfranceschi, F. Venti & E. Romano
(2012). Correlation
between textural characteristics of marine sediments and benthic foraminifera
in highly anthropogenically-altered coastal areas. Marine Geology
315–318: 143–161. https://doi.org/10.1016/j.margeo.2012.04.002
Martina,
P., T.E. Roberts & J.M. Pandolfi (2017). Variation in sensitivity of large benthic
Foraminifera to the combined effects of ocean warming and local impacts. Scientific
Reports 7: 45227.
Mariéva,
D., F.J. Jorissen, D. Martin, F. Galgani & J. Miné (2010). Comparison of benthic
foraminifera and macro faunal indicators of the impact of oil-based drill mud
disposal. Marine Pollution Bulletin 60(11): 2007–2021. https://doi.org/10.1016/j.marpolbul.2010.07.024
Murray, J.
(2006). Chapter 10:
Application. Ecology and Applications of Benthic Foraminifera. Cambridge
University Press, England, 281 pp.
Patricia
P.B.E., A.R. Rodrigues, M.P. Gomes & H. Vital (2019). Benthic
foraminifera as indicators of river discharge in the Western South Atlantic
continental shelf. Marine Geology 415: 105973. https://doi.org/10.1016/j.margeo.2019.105973
Pierre,
A.D., J. Bonnin, J.H. Kim, S. Bichon, B. Deflandre, A. Grémare & J.S.S.
Damsté (2016). Impact of organic matter source and quality on living benthic
foraminiferal distribution on a river-dominated continental, margin: a study of
the Portuguese margin. Journal of Geophysical Research: Biogeosciences
121(6): 1689–1714. https://doi.org/10.1002/2015JG003231
Pravasini,
P. & P.K. Patra (2012). Benthic foraminiferal responses to coastal pollution: a review. International
Journal of Geology, Earth and Environmental Sciences 2(1): 42–56.
Rajiv, N. (1986). Foraminiferal assemblages and their use as
indicators of sediment movement: a study in the shelf region off Navapur,
India. Continental Shelf Research 5(4): 421–431.
Rehab, E.,
M.I. Ibrahim, Y. Milker, G. Schmiedl, N. Badr, S.E.A. Kholeif & K.A.F.
Zonneveld (2011). Anthropogenic impact on benthic foraminifera, Abu-Qir bay, Alexandria,
Egypt. Journal of Foraminiferal Research 41(4): 326–348. https://doi.org/10.2113/gsjfr.41.4.326
Ritesh, V.,
V.K. Kushwaha, N. Pandey, T. Nandy & S.R. Wate (2015). Extent of sewage
pollution in coastal environment of Mumbai, India: an object-based image
analysis. Water and Environment Journal 29: 365–374. https://doi.org/10.1111/wej.12115
Shamrao,
A.I. & A.N. Kadam (2003). Pollution of some recreation beaches of Mumbai,
Maharashtra. Journal of Indian Association of Environmental Management
30: 172–175.
Singare,
P.U., S.E.L. Ferns & E.R. Agharia (2015). Studies on Toxic
Heavy Metals in Sediment Ecosystem of Mahim Creek near Mumbai, India. International
Letters of Chemistry, Physics and Astronomy 43: 62–70. https://doi.org/10.18052/www.scipress.com/ILCPA.43.62
Subhadra,
D.G. & R.K. Patil (2012). Comparative study on foraminifera of east and
west coast of India. Journal of Environmental Biology 33: 903–908.
Sundara,
R.R.B.C., N. Jayaraju, G. Sreenivasulu, U. Suresh & A.N. Reddy (2016). Heavy metal
pollution monitoring with foraminifera in the estuaries of Nellore coast, East
coast of India. Marine Pollution Bulletin 113(1–2): 542–551. https://doi.org/10.1016/j.marpolbul.2016.08.051
Suresh,
M.G. & A.N. Sonia (2012). Benthic foraminifera and geochemical studies with
influence on pollution studies along the coast of Cuddalore, Tamil Nadu-ITS,
India.Arabian Journal of Geosciences 7: 917–925. https://doi.org/10.1007/s12517-012-0775-3
Syed, A.K.,
K.G.M.T. Ansari & P.S. Lyla (2011). Organic matter content of sediments in
continental shelf area of southeast coast of India. Environmental Monitoring
and Assessment 184: 7247–7256.
Vidya, P.
& R.K. Patil (2014). Mangrove sediment core analysis of foraminiferal assemblages - a study
at two sites along the western coast of India. Journal of Threatened Taxa 6(2):
5485–5491. https://doi.org/10.11609/JoTT.o3653.5485-91
Walton, W.R. (1952). Techniques for
recognition of living foraminifera. Contributions from the Cushman
Foundation for Foraminiferal Research 3: 56–60.