Journal of Threatened Taxa |
www.threatenedtaxa.org | 26 May 2023 | 15(5): 23190–23199
ISSN 0974-7907 (Online) | ISSN 0974-7893
(Print)
https://doi.org/10.11609/jott.8277.15.5.23190-23199
#8277 | Received 22 November 2022 | Final
received 27 February 2023 | Finally accepted 11 May 2023
Effect of ecological factors on the grass dynamics at Point Calimere Wildlife Sanctuary, India
Selvarasu Sathishkumar
1, Subhasish Arandhara
2 & Nagarajan Baskaran 3
1,2,3 Mammalian Biology
Lab, Department of Zoology, A.V.C. College (Autonomous) (affiliated to
Bharathidasan University, Tiruchirappalli), Mannampandal,
Tamil Nadu 609305, India.
1 ksathish605@gmail.com,
2 subhasisharandhara@gmail.com, 3 nagarajan.baskaran@gmail.com
(corresponding author)
Editor: P. Ravichandran, Manonmaniam
Sundaranar University, Thirunelveli,
India. Date of publication: 26
May 2023 (online & print)
Citation: Sathishkumar, S., S. Arandhara & N. Baskaran (2023). Effect of ecological factors on the
grass dynamics at Point Calimere Wildlife Sanctuary,
India. Journal of Threatened Taxa 15(5): 23190–23199. https://doi.org/10.11609/jott.8277.15.5.23190-23199
Copyright: © Sathishkumar 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: The project was funded by Science and Engineering Research Board [Grant File. No. EMR/2016/001536], Dept. of
Science and Technology, New Delhi, Govt. of India.
Competing interests: The authors declare no competing interests.
Author details: Selvarasu Sathishkumar is presently a PhD scholar in A.V.C. College (Autonomous), (affiliated to Bharathidasan University, Tiruchirappalli), Mayiladuthurai, Tamil Nadu, India. Subhasish Arandhara is presently a PhD scholar in A.V.C. College (Autonomous), (affiliated to Bharathidasan University, Tiruchirappalli), Mayiladuthurai, Tamil Nadu, India. Nagarajan Baskaran is an assistant professor at the Department of Zoology, A.V.C. College (Autonomous) since 2011. Worked as senior scientist at Asian Elephant Research & Conservation
Centre, Centre for Ecological Sciences, Indian Institute of Science, Bangalore during 2002–2011. Research Interest: Studying the behavioural ecology of Wild Asian Elephants and their habitats in southern Indian, east-central Indian (Eastern & Western Ghats) and parts of northeastern India (eastern Himalaya), since 1990. Also studying other large mammals like antelopes, squirrels, sloth bears and assessing biodiversity and impact of developmental activities on conservation of biodiversity in India.
Author contributions: SS—data collection and analyses, draft preparation. SA—data collection, pruning, and analyses and draft preparation. NB—conceptualizing, supervising, data analyses, and final draft preparation.
Acknowledgements: This work was supported by the Science and
Engineering Research Board [Grant File. No. EMR/2016/001536], Dept. of Science
and Technology, New Delhi, Govt. of India. We express our sincere thanks to the
Tamil Nadu Forest Department, especially its former chief wildlife wardens, Mr.
P.C. Thyagi, I.F.S. and Sanjay Kumar Srivastava,
I.F.S., and the wildlife warden Point Calimere, Nagapattinam for granting permission to conduct the study
and support to it. We are also thankful to the management and the principal of
A.V.C. College for their constant support to this project.
Abstract: Grass dynamics play a
major role in the density and diversity of grazing mammals. To understand the
drivers of grass quality and quantity, we assessed the height, cover,
soft-texture, green leaves, and reproductive phase of grass species in relation
to 13 ecological covariates belonging to climate, vegetation, human
disturbance, and wild herbivores at Point Calimere
Wildlife Sanctuary, southern India during November 2018─September 2020. From
the 1,024 quadrates, we recorded 22 grass species and 10 sedges. The grass
parameters varied significantly among habitats and between seasons. The grass
height and grass cover were more in open scrub, while the soft-textured green
grasses were more in grasslands. All the grass parameters except reproductive
stage were highest during the wet season. The general linear model (GLM) based
analysis on the covariate effect on grass quantity and quality demonstrated
that among the 13 covariates compared, Prosopis, an alien invasive
species, is the major driver, with negative influence on both grass quantity;
the cover, and grass quality; soft-texture and greenness of grass. The feral
horse, an alien invasive, negatively influenced grass height. Earlier studies
have also shown the devastating effects of these exotics on native flora and
fauna at Point Calimere, and measures suggested by
these studies are recommended to safeguard natural communities in the area.
Keywords: Dry evergreen,
grasslands, grass quality, greenness of grass, invasive threat, open scrub,
soft-textured grass, southern India, species composition, Tamil Nadu.
Introduction
In
grassland environment grass phenology regulates the life cycles of grasses,
which has a direct impact on biodiversity and trophic levels associated to
herbivory (Auken 2009; Fischer et al. 2013).
Phenology of grass species such as fledgling grass, soft shoots, soft, and
green leaves determine herbivore nutrients (Hughes et al. 1993). Leaf length,
leaf size, and spruce growth are unique features of each species (Ahsan et al.
2010; Huijser & Schmid 2011; Wang et al. 2011).
The growth rate depends on the life cycle of the grass species. At the
vegetative phase, cellulose and hemicellulose are present in large quantities
for energy supply (Islam et al. 2003; Hussain & Durrani
2009). The budding, flowering, fruiting to seed dispersal stages are the
reproductive phases (Sherry et al. 2011). Many factors, including rainfall,
soil type, season, access to water, and the availability of open habitat play a
role in determining the quantity and quality of grass that can grow (Ganskopp & Bohnert 2001;
Sawyer et al. 2005; Hagenah et al. 2008; Hussain & Durrani
2009; Zeng et al. 2010).
Grasslands
are significant global reservoirs of biodiversity and important food sources
for herbivores (Jing et al. 2014; White et al. 2000; Bardgett
et al. 2021). Natural grasslands are also vital to climate and water
regulation, and to biogeochemical cycles like carbon balance, hence their
degradation has serious consequences (White et al. 2000; O’Mara 2012; Cai et
al. 2015). Natural grasslands cover regions with sufficient precipitation for
grass to grow. Climatic, human-caused, and other environmental factors
influence grasslands and alter grass phenology (Boval
& Dixon 2012). Worldwide, grasslands have been disappearing for the greater
part of a century (Egoh et al. 2016). In a short
amount of time, grassland can be negatively affected by a shift in land use.
Specifically, a major issue with grasslands is the growth and succession of
forests (Liu et al. 2013).
This
study focuses on the grass species of Point Calimere
Wildlife Sanctuary, which acts as the major food source to the Blackbuck, an
iconic species of the reserve, and other ungulates. Multiple pressures, from
the invasion of Prosopis to over-grazing by cattle and feral horse on
the grasslands habitat, would result in decline in grass biomass needed to
support the Blackbuck population in the study area (Baskaran et al. 2016; Arandhara et al. 2020, 2021). Although grasses have wide
ecological amplitude and several adaptations to withstand trampling, grazing,
fire, food, and drought, they face severe competition for light and nutrients
from aggressive wood species and invasive plants in tropical forests (Ashokkumar et al. 2021). This study assessed grass species
parameters representing quantity: height & cover, and quality: grass
soft-texture, green grass, & reproductive phase, across three habitats and
two seasons between 2018─2020 to identify the ecological drivers of grass
quantity and quality.
Methods
Study
area
The
research was carried out at the Point Calimere
Wildlife Sanctuary in Tamil Nadu, which is located between 10.30–79.85 0N
and 10.35–79.42 0E at the confluence of the Bay of Bengal and the
Palk Strait, near Nagapattinam (Figure 1). The
reserve encompasses 30 km2 of dry evergreen forest, grassland, open
scrub, sandy coastline, salt marshes, and backwaters (Ali 2005). The grasses in
the sanctuary’s southernmost region cover 17% (4.49 km2) of the
total sanctuary area. The sanctuary’s native and flagship species of Blackbuck
live in grasslands that also serve as a foraging ground for other herbivores
like feral horses, Chital, and domestic cattle. The average annual rainfall in
Point Calimere is 1,366 mm, with temperatures ranging
23─37 ºC. The grasslands are especially vulnerable to invasion by
Prosopis juliflora. Anthropogenic pressures on
the sanctuary include firewood collection, fishing, and cattle grazing.
Data
collection
Assessment
of Grass dynamics and other variables: Data were collected between November
2018 and October 2020 covering two seasons (dry season: February─August
and wet season: September─January) and three habitats
(Dry evergreen, open scrub, and grasslands). The study area was overlaid with 1
km2 grids and placed with a 1-km line transect at each grid. The
grass availability and parameters were evaluated on a monthly interval. Four 1
m2 quadrates were placed at 5 m intervals on the north, south, east,
and west directions at every 250 m interval along these transects. Quadrates of
this size have previously been widely used in studies of grass abundance (Menut & Ceaser 1979; Hacker
1984; Sivaganesan 1991). In total, 1,024 quadrates
were laid (dry evergreen—453, open scrub—272, and grasslands—299) (Image 1).
All grass dynamic parameters were recorded in each quadrat following methods
described in Table 1 Grass specimens were collected and preserved in order to
create herbariums for each grass species for species identification and
confirmation (Rangel et al. 1999; Shaw 2008; Shankar & Shashikala 2010).
The vouchered herbarium was deposited at mammalian biology lab, department of
Zoology in A.V.C. College (Autonomous).
Data
analysis
Statistical
analysis: Prior to performing a detailed analysis, the compiled data were
examined for normality and variance homogeneity. The Kolmogorov-Smirnov (KS)
test used on grass parameter such as, height (KS: 0.35; p = <0.05),
cover (KS: 0.19; p = <0.05), soft texture (KS: 0.23; p =
<0.05), green leaves (KS: 0.16; p = <0.05), and reproductive phase
(KS: 0.37; p = <0.05) of grass species was neither normal, nor could
be transformed to normal with four different transformations (Arsin, Log10 (LG10), Inverse log, and Exponential).
Therefore, the difference in the selection of this species between seasons were
tested using non-parametric Mann-Whitney U-test and Kruskal-Wallis H test. SPSS
V.23 software package was used for the statistical test and the general linear
model (GLM) was used to identify the covariates influencing on grass dynamics
characteristics and all parameter models were ranked by their small-sample
Akaike information criterion (AICc) and inferences
were taken from models with ΔAICc ≤ 2. However, in
results are comprehensively shows that top two models of lowest ΔAICc. Model comparison were calculated by the R
package ‘MuMIn’ (Barton et al. 2018) by in R Library,
in R Software Version 3.3.3 (R Core Team 2019). This model was ranked first due
to lowest AIC. Also, the proportion of the total predictive power found in the
model was sorted to be the highest at weight value. The analysis was carried
out for each grass parameter separately.
Results
In
total, the study identified 22 grass species and 10 species of sedges at Point Calimere (Table 2). The grass species dominated the stand
in all parameters studied compared to sedges. Aeluropus
lagopoides had the highest mean height,
percentage of cover, soft texture, and green leaves. Chloris barbata had the highest percentage of reproductive
phase. Dactyloctenium aegyptium
was the second highest in terms of cover, soft texture green leaves,
followed by Cyperus compressus.
Variation
in grass parameters between season and among habitats
The
grass parameters varied significantly among the three habitats: grassland,
open-scrub, and dry evergreen. Among the five grass parameters, grass height,
percentage cover, and reproductive phase were significantly more in open-scrub
followed by grasslands and dry evergreen (Figure 2). On the other hand,
soft-textured grass and green leaves were significantly higher in grasslands
than the other two habitats. In relation to season, grass height, percentage
cover, soft texture, and green leaves were significantly higher in the wet
compared to dry season. While the reproductive stage was significantly higher
during dry compared to wet season (Table 3).
Influence
of covariates on grass parameter - GLM Model
Grass
height: GLM to test the influence of
covariates on grass height showed a model with covariates viz feral-horse
density, P. juliflora cover, rainfall, spotted
deer density, shrub % cover, and distance from water bodies turned out as the
best model with lower delta AIC and higher weightage, influencing the grass
height (Table 4). However, the covariates, viz., feral-horse with negative influence
and rainfall with positive influence were alone turned out to be the
significant predictors of grass height (Table 5).
Grass
cover: Although the GLM showed that
covariates with feral-horse density, grasslands, P. juliflora
cover, rainfall and distance from water bodies entered as the best model with
lower delta AIC and higher weightage influencing the grass cover (Table 4),
covariates, viz., feral-horse, P. juliflora
cover, distance from water with negative influence, and rainfall and wet season
with positive influence turned out to be the significant predictors of grass
cover (Table 5).
Grass
soft-texture: A model with open habitat, P.
juliflora density, rainfall and distance from
shade entered as the best model with lower delta AIC and higher weightage
influenced the soft-texture of grass (Table 4). Interestingly, all the four
covariates had significant effect on the soft-texture with rainfall, open
habitat, and distance from shade were having positive influence, while the P.
juliflora density had negative influence (Table
5).
Grass
green leaves: Although a model with blackbuck
density, open habitat, P. juliflora density,
and rainfall entered as the best model with lower delta AIC and higher
weightage influencing the green leaves availability (Table 4), covariates,
viz., density of P. juliflora and blackbuck
with negative effect and open habitat with positive effect were alone
significantly influencing the percentage of green leaves in the grass species
(Table 5).
Grass
reproductive phase: Although a model with
covariates such as feral-horse density, open habitat extent, P. juliflora density, and rainfall entered as the best
model with lower delta AIC and higher weightage influencing the reproductive
phase of the grass (Table 4), covariates, viz., P. juliflora
density and open-scrub with positive effect and rainfall with negative effect
had significant influence on the amount of grass reproductive phase (Table 5).
Discussion
This
study observed 22 species of grasses and 10 sedges in the study area, similar
to what Arandhara et al. (2021) and Frank et al.
(2021) reported for the same area. On the basis of cover, species such as A.
lagopoides, D. aegyptium,
and C. compressus are the three
dominant grasses recorded in the coastal habitats, open-scrub, and
dry-evergreen in this study. These findings also support earlier studies
elsewhere for A. lagopoides (Khan & Gulzar
2003; Ahmed et al. 2013), D. aegyptium
(Rojas-Sandoval 2016), and C. compressus
(Ravi & Mohanan 2002; Bryson & Carter 2008).
Independent
factors influencing the grass parameters
Rainfall,
wet season, open habitat availability, distance from shade, and open-scrub
habitat all had a positive impact on the grass parameters measured at Point Calimere. In contrast, Prosopis juliflora,
the density of feral horse and Blackbuck, and the distance from water
negatively influenced the grass parameters studied.
Predictors
of grass height
The
density of feral horses, a non-ruminant bulk feeder (Arandhara
et al. 2020), had the greatest negative effect on grass height among the
13 covariates compared. According to Maron &
Crone (2006), the effects of herbivory on grassland are more severe than those
on woodland. Rainfall, widely regarded as the most effective factor in
promoting plant growth, was a major predictor influencing positively on height
of the grass species (Derner & Hart 2007; Parton
et al. 2012). Increased rainfall during the growing season has been shown to
improve soil water use, which in turn promotes healthy root development and
grasses as well as other plant growth (Wan et al. 2002).
Predictors
of grass cover
The
study showed that percentage of grass cover decreased with feral horse density,
P. juliflora cover and distance from the
waterbody. The feral-horse is a large herbivore with predominant grazing nature
and a bulk-feeder (Baskaran et al. 2019; Arandhara et
al. 2020). Their intensive grazing pressure is thus negatively influencing the
grass cover, as grazing mostly occurs during the growing season (Hao & He
2019). In this study, a decrease in grass cover was observed with the Prosopis
cover. Prosopis is an alien invasive species at Point Calimere, which grow taller and tap the sunlight at canopy
level. Sunlight is an essential factor for the photosynthesis of all plants
including grass species and thus the increase in Prosopis cover reduces
the intensity of sunlight available to the grass species found at the ground
level. Therefore, grass cover decreased with Prosopis cover (Baskaran et
al. 2019; Murugan et al. 2019; Arandhara
et al. 2021). Like the sunlight, soil nutrient, soil moisture is also another
important factor influences the plant growth and productivity and moisture in
the soil is required during the wet season to promote CO2 absorption
and plant growth (Morgan et al. 2016). Therefore, the grass cover increased
significantly with rainfall and during wet season compared to dry season as
reported elsewhere (Wan et al. 2002; Zhang et al. 2020; Xu et al. 2021). Since
soil moisture decreases with increase in distance from waterbody, the grass
cover decreased significantly with distance from the waterbody.
Predictors
of soft-texture and green grass
The
study showed that grass soft-texture increased with rainfall, open habitat, and
distance from the shade, but it decreased with Prosopis density.
Similarly, the green grass availability increased with rainfall, and open
habitat, but it decreased with Prosopis and blackbuck densities. Studies
have shown that rainfall by increasing the soil moisture, triggering the growth
of fresh, and green grasses (Hermance et al. 2015;
Moore et al. 2015; Morgan et al. 2016; Post & Knapp 2020). The fact that
fresh grown plants parts are softer than the old-grown parts due to low fiber
and cellulose content (de Jong 1995; Treydte et al.
2011; Kunwar et al. 2016). Thus, rainfall increases significantly both
soft-texture and green leaves of grasses. The open habitat provides the ideal
sunlight intensity and temperature for promoting photosynthesis in grass
species (Solofondranohatra et al. 2018) and thus the
soft-textured green grasses increased significantly with extent of open
habitats. In contrast, with increase in Prosopis density, which exploits
both sunlight at canopy level and the available soil moisture more efficiently
(Shiferaw et al. 2021), reduces the soft-texture and
greenness of the grass species through reduced growth. The negative effect of
shade on grass soft-texture also follows the above concept as explained for Prosopis.
Blackbucks are a species of ruminant that is known for eating the tips of
young, tender grass leaves, which are richer nutrients and water content (Jhala 1997; Baskaran et al. 2016) and thus green grass
availability decreases with the density of blackbucks.
Predictors
of grass reproductive phase
The
study shows that the grass species reproductive phase increased with P. juliflora cover and open-scrub. As stated in earlier
studies that the open-scrub predominantly with woody plants that are typically
less than 3 m tall and relatively open, offers excellent support for grasses
and plants that are shorter than them (Wardle 1971; Solofondranohatra
et al. 2018). Likewise, P. juliflora is the
most common woody plant in open-scrub at Point Calimere
(Arandhara et al. 2021). Since, grazers are unable to
access the grass species found between and beneath the bushes, the grazing
intensity is lower in open-scrub compared to grasslands. Thus, the grass
species with less grazing pressure in the open-scrub or with more density of Prosopis,
with better growth as found in this study, had more reproductive phases than
that of in grasslands. These findings are similar to earlier study that states
the grass species in the open-scrub were shielded from overgrazing (Popay & Field 1996). As a result, the grass species
reaches its maximum potential for growth and reproduction. As the mean annual
precipitation across space increased, flowering time pushed back for most grass
species, as documented by Munson & Long (2017).
Conclusions and recommendations
Point
Calimere supports grasses and sedges which provide
ideal food sources for mammalian grazing communities. Both grass species
quantity and quality varied among habitats and between seasons. Among the 13
covariates compared, Prosopis, an alien invasive species, is the major
driver that negatively influences on both grass quantity and quality. The feral
horse, an alien invasive, negatively affected grass height. The devastating
effect of these exotics on native flora and fauna at Point Calimere
have been already documented by various studies (Ali 2005; Baskaran et al.
2019; Arandhara et al. 2020, 2021). Thus, to
safeguard the natural communities of plants and animals of Point Calimere, effective measures are needed as suggested by
earlier studies.
Table 1. Details of
grass dynamics parameters and covariates sampled at Point Calimere
Wildlife Sanctuary, India.
|
|
Grass dynamics
parameters |
Description |
|
Dependent variables |
||
|
1 |
Grass height (cm) |
Grass height was
measured using a measuring scale, from the ground level to the highest leaf
blade bend, at five points (one each at four corners and one at the center)
of the quadrate. |
|
2 |
Grass cover/m2 |
Assessed visually
assuming 100% for the entire quadrat and estimating the proportion of area
within a quadrat covered by each grass. |
|
3 |
Soft texture (%) |
Examined crushing
the leaves by hands, if leaf’s structure could be squashed into a
ball—proportion of such leaves for a given grass species in quadrat was rated
in % rating. |
|
4 |
Green leaves (%) |
Assessed visually
quantifying the proportion of leaves in a given species with green grass,
assuming 100% for all the leaves of the same species. |
|
5 |
Reproductive phase
(%) |
Evaluated visually
quantifying the proportion of a given grass with flowers and fruits in %
rating. |
|
Covariates |
||
|
6 |
Open habitat extent
(km2) |
At every plot laid,
habitat visibility on all four directions of north, south, east, and west. |
|
7 |
Distance to water
(m) |
Measured as the
distance from a given quadrate to the water source using a rangefinder or
obtained from land-use land-cover map. |
|
8 |
Distance to shade
(m) |
Measured as the
distance from a given quadrat to the nearest canopy cover area using a
rangefinder. |
|
9 |
Distance to road
(m) |
Measured as the
distance from a given quadrat location to the nearest road or obtained from
land-use land-cover map. |
|
10 |
Ambient temperature
(°C) |
Measured using a
generic digital thermometer-cum-hygrometer device (model: HT01) at each
observation at the feeding site. |
|
11 |
Humidity (Relative
%) |
As described above. |
|
12 |
Weather |
Recorded visually
as cloudy or sunny weather at the start of each feeding site examination. |
|
13 |
Rainfall (mm) |
Rainfall data
arrived from the secondary sources
(https://www.soda-pro.com/web-services/meteo-data/merra) |
|
14 |
Prosopis juliflora cover/25 m2 |
Prosopis density were
arrived from 5 x 5 m quadrates in the study area |
|
15 |
Prosopis juliflora density/25 m2 |
Prosopis cover were
obtained from 5 x 5 m quadrates in the study area |
|
16 |
Blackbuck density |
Density was
obtained by the line transect survey method in the study area. |
|
17 |
Feral horse density |
As described above |
|
18 |
Chital density |
As described above. |
Table 2. Overall list
of grass and sedge species and their parameter recorded at Point Calimere Wildlife Sanctuary, India.
|
|
Grass and sedge
species |
Height (cm) |
Cover (%) |
Soft texture (%) |
Green leaves (%) |
Reproductive phase
(%) |
|
|
Grasses |
|||||||
|
1 |
Aeluropus lagopoides (L.) |
13.2 ± 0.9 |
20.3 ± 1.5 |
20.3 ± 1.5 |
20.4 ± 1.5 |
6.1 ± 0.4 |
|
|
2 |
Aristida adscensionis (L.) |
1.0 ± 0.4 |
0.7 ± 0.3 |
0.7 ± 0.3 |
0.7 ± 0.3 |
0.3 ± 0.1 |
|
|
3 |
Aristida setacea (Retz.) |
1.4 ± 0.4 |
1.3 ± 0.4 |
1.3 ± 0.4 |
1.2 ± 0.4 |
0.0 ± 0.0 |
|
|
4 |
Brachiaria ramosa (L.) Stapf. |
2.4 ± 0.4 |
3.8 ± 0.6 |
3.8 ± 0.6 |
3.8 ± 0.6 |
1.3 ± 0.2 |
|
|
5 |
Cenchrus ciliaris (L.) |
1.5 ± 0.6 |
0.7 ± 0.3 |
0.7 ± 0.3 |
0.7 ± 0.3 |
1.4 ± 0.6 |
|
|
6 |
Chloris barbata Sw. |
10.6 ± 1.2 |
7.6 ± 0.9 |
7.5 ± 0.9 |
7.4 ± 0.9 |
13.0 ± 1.5 |
|
|
7 |
Chrysopogon aciculatus (Retz.) Trin. |
4.8 ± 1.1 |
1.7 ± 0.4 |
1.7 ± 0.4 |
1.7 ± 0.4 |
4.6 ± 1.1 |
|
|
8 |
Chrysopogon fulvus (Spreng.) Chiov. |
2.6 ± 0.8 |
1.1 ± 0.3 |
1.1 ± 0.3 |
1.0 ± 0.3 |
2.9 ± 0.9 |
|
|
9 |
Cynodon dactylon (L.) Pers. |
0.1 ± 0.1 |
0.4 ± 0.2 |
0.4 ± 0.2 |
0.4 ± 0.2 |
0.3 ± 0.2 |
|
|
10 |
Cyrtococum trigonum (Retz.) A.Camus |
0.4 ± 0.2 |
0.4 ± 0.2 |
0.4 ± 0.2 |
0.4 ± 0.3 |
0.6 ± 0.3 |
|
|
11 |
Dactyloctenium aegyptium (L.) Willd. |
5.8 ± 0.5 |
12.4 ± 1.2 |
12.6 ± 1.2 |
12.8 ± 1.2 |
12.2 ± 1.1 |
|
|
12 |
Dichanthium annulatum (Forssk.)
Stapf |
3.6 ± 1.1 |
1.1 ± 0.3 |
1.1 ± 0.3 |
1.1 ± 0.3 |
0.6 ± 0.2 |
|
|
13 |
Digitaria longiflora (Retz.) Pers. |
1.2 ± 0.3 |
1.2 ± 0.3 |
1.2 ± 0.4 |
1.3 ± 0.4 |
1.9 ± 0.5 |
|
|
14 |
Eragrostiella bifaria (Vahl) Bor. |
0.6 ± 0.2 |
0.6 ± 0.2 |
0.6 ± 0.2 |
0.6 ± 0.2 |
0.9 ± 0.4 |
|
|
15 |
Eriochloa procera (Retz.) C.E.Hubb. |
0.7 ± 0.3 |
0.8 ± 0.3 |
0.8 ± 0.3 |
0.8 ± 0.3 |
0.9 ± 0.3 |
|
|
16 |
Hemarthria compressa (L.f.)
R.Br. |
0.6 ± 0.4 |
0.3 ± 0.2 |
0.3 ± 0.2 |
0.3 ± 0.2 |
0.3 ± 0.2 |
|
|
17 |
Heteropogon contortus (L.) P.Beauv.
ex Roem. & Schult. |
2.7 ± 1.3 |
0.4 ± 0.2 |
0.4 ± 0.2 |
0.4 ± 0.2 |
0.3 ± 0.1 |
|
|
18 |
Megathyrsus maximus (Jacq.) B.K.Simon & S.W.L.Jacobs,
2003 |
1.9 ± 0.8 |
0.7 ± 0.3 |
0.7 ± 0.3 |
0.7 ± 0.3 |
0.6 ± 0.2 |
|
|
19 |
Oplismenus composites (L.) P. Beauv. |
1.9 ± 0.5 |
1.6 ± 0.4 |
1.5 ± 0.4 |
1.5 ± 0.4 |
3.1 ± 0.8 |
|
|
20 |
Paspalum paspaloides (L.) |
1.3 ± 0.6 |
0.5 ± 0.2 |
0.5 ± 0.2 |
0.5 ± 0.2 |
0.0 ± 0.0 |
|
|
21 |
Perotis indica (L.) |
10.0 ± 1.6 |
4.1 ± 0.7 |
4.0 ± 0.7 |
4.0 ± 0.6 |
9.0 ± 1.5 |
|
|
22 |
Trachys muricata (L.) Pers. |
0.2 ± 0.2 |
0.0 ± 0.0 |
0.0 ± 0.0 |
0.0 ± 0.0 |
0.3 ± 0.3 |
|
|
Sedges |
|||||||
|
23 |
Bulbostylis barbata (Rottb.) C.B.Clarke |
2.9 ± 0.5 |
3.8 ± 0.6 |
3.8 ± 0.6 |
3.8 ± 0.6 |
6.2 ± 1.0 |
|
|
24 |
Cyperus compressus (L.) |
5.5 ± 0.6 |
10.2 ± 1.0 |
10.2 ± 1.0 |
10.1 ± 1.0 |
5.6 ± 0.6 |
|
|
25 |
Cyperus kyllingia (L.) |
1.8 ± 0.3 |
3.3 ± 0.6 |
3.4 ± 0.6 |
3.4 ± 0.6 |
1.2 ± 0.2 |
|
|
26 |
Cyperus polystachyos Rottb. |
2.4 ± 0.4 |
3.3 ± 0.6 |
3.2 ± 0.6 |
3.2 ± 0.6 |
2.5 ± 0.4 |
|
|
27 |
Cyperus rotundus (L.) |
0.9 ± 0.3 |
1.3 ± 0.4 |
1.4 ± 0.4 |
1.4 ± 0.4 |
0.3 ± 0.1 |
|
|
28 |
Cyperus squarrosus (L.) |
1.2 ± 0.3 |
1.8 ± 0.4 |
1.8 ± 0.4 |
1.8 ± 0.4 |
0.6 ± 0.1 |
|
|
29 |
Fimbristylis cymosa R.Br. |
8.9 ± 1.1 |
6.9 ± 0.8 |
7.0 ± 0.9 |
7.0 ± 0.9 |
11.3 ± 1.4 |
|
|
30 |
Fimbristylis ovata (Burm.f.) J.Kern |
0.3 ± 0.1 |
0.6 ± 0.3 |
0.6 ± 0.3 |
0.6 ± 0.3 |
0.6 ± 0.3 |
|
|
31 |
Fimbristylis triflora (L.) K.Schum. |
3.0 ± 0.6 |
2.2 ± 0.5 |
2.2 ± 0.5 |
2.2 ± 0.5 |
4.6 ± 1.0 |
|
|
32 |
Kyllinga nemoralis (J.R.Forst.
& G.Forst.) Dandy ex Hutch. & Dalziel |
4.9 ± 0.7 |
4.9 ± 0.7 |
4.9 ± 0.7 |
5.0 ± 0.7 |
6.8 ± 1.0 |
|
Table 3. Seasonal
variation among the grass parameter at Point Calimere
Wildlife Sanctuary, India.
|
Grass dynamics
parameters |
Wet season (n =
592) |
Dry season (n =
432) |
Mann-Whitney U |
p |
|
Height (cm) |
13.4 ± 1.43 |
10.1 ± 0.26 |
17224 |
0.000 |
|
Cover (%) |
24.7 ± 0.78 |
21.6 ± 0.89 |
40389 |
0.000 |
|
Soft texture (%) |
67.1 ± 1.75 |
47.6 ± 1.58 |
24379 |
0.000 |
|
Green leaves (%) |
75.7 ± 0.80 |
37.6 ± 0.82 |
69701 |
0.000 |
|
Reproductive phase
(%) |
36.4 ± 1.82 |
43.5 ± 2.24 |
31091 |
0.001 |
Table 4. Top two best
models extracted from GLM to characterize relationship among the grass
parameter and the covariates sorted according to AIC.
|
Dependent variables |
Model |
df |
Log L |
AICc |
∆AICc |
weight |
|
Grass height (cm) |
Feral-horse density
+ Prosopis juliflora cover + rainfall +
Spotted deer density + Shrub percentage cover + Distance from water bodies |
5 |
-3258 |
6527 |
0.00 |
0.099 |
|
Feral-horse density
+ Spotted deer density + Shrub percentage cover |
4 |
-3259 |
6527 |
0.20 |
0.090 |
|
|
Grass cover (%) |
Feral-horse density
+ Grassland habitat + Prosopis juliflora
cover + rainfall + Distance from water bodies |
8 |
-4544 |
9105 |
0.00 |
0.091 |
|
Feral-horse density
+ Grassland habitat + Prosopis juliflora
cover + rainfall + Shrub percentage cover + Distance from water bodies |
9 |
-4543 |
9106 |
0.28 |
0.079 |
|
|
Grass soft texture
(%) |
Open habitat
availability+ Prosopis juliflora density +
rainfall + Distance from shade |
5 |
-4995 |
10001 |
0.00 |
0.996 |
|
Open habitat
availability+ Prosopis juliflora density +
rainfall |
4 |
-5002 |
10013 |
1.51 |
0.002 |
|
|
Grass green leaves
(%) |
Blackbuck density +
Open habitat availability + Prosopis juliflora
density + rainfall |
6 |
-5496 |
11004 |
0.00 |
0.650 |
|
Blackbuck density +
Open habitat availability + Prosopis juliflora
density |
5 |
-5498 |
11006 |
1.60 |
0.292 |
|
|
Grass reproductive
phase (%) |
Prosopis juliflora cover + rainfall + Open-scrub |
5 |
-4965 |
11098 |
0.00 |
0.880 |
|
Prosopis juliflora cover + rainfall + Open-scrub |
4 |
-4910 |
11088 |
1.04 |
0.652 |
Table 5. The best
model showing the relationship between each grass variable and the significant
covariates.
|
Dependent variable |
Covariate |
Estimate ± S.E. |
z value |
Pr(>|z|) |
|
Grass height (cm) |
(Intercept) |
10.6 ± 0.59 |
17.95 |
0.000 |
|
Feral horse density |
-0.0 ± 0.01 |
3.28 |
0.001 |
|
|
Rainfall |
0.1 ± 0.00 |
0.64 |
0.022 |
|
|
Grass cover (%) |
(Intercept) |
42.2 ± 0.02 |
251.41 |
0.000 |
|
Feral horse density |
-0.0 ± 0.00 |
11.40 |
0.000 |
|
|
P. juliflora cover |
-0.0 ± 0.01 |
14.65 |
0.000 |
|
|
Rainfall |
0.0 ± 0.02 |
3.21 |
0.001 |
|
|
Wet season |
0.1 ± 0.01 |
4.28 |
0.000 |
|
|
Distance from water |
-0.0 ± 0.02 |
2.80 |
0.005 |
|
|
Grass soft texture
(%) |
(Intercept) |
4.0 ± 1.79 |
223.28 |
0.000 |
|
Rainfall |
0.0 ± 0.02 |
4.97 |
0.000 |
|
|
P. juliflora density |
-1.1 ± 0.12 |
-9.70 |
0.000 |
|
|
Open habitat
availability |
0.0 ± 0.02 |
3.83 |
0.000 |
|
|
Distance from shade |
0.0 ± 0.02 |
-3.80 |
0.000 |
|
|
Grass green leaves
(%) |
(Intercept) |
4.0 ± 0.02 |
223.64 |
0.000 |
|
Rainfall |
0.0 ± 0.02 |
4.16 |
0.000 |
|
|
P. juliflora density |
-1.0 ± 0.12 |
-8.62 |
0.000 |
|
|
Open habitat
availability |
0.0 ± 0.02 |
3.52 |
0.000 |
|
|
Blackbuck density |
-512 ± 179.3 |
-2.86 |
0.004 |
|
|
Grass reproductive
phase (%) |
(Intercept) |
39.4 ± 5.29 |
7.44 |
0.000 |
|
P. juliflora cover |
0.82 ± 0.33 |
2.46 |
0.013 |
|
|
Rainfall |
-0.10 ± 0.01 |
-6.25 |
0.000 |
|
|
Open scrub |
1.8 ± 0.89 |
0.04 |
0.048 |
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References
Ahmed, M.Z., T. Shimazaki, S. Gulzar, A. Kikuchi, B. Gul, M.A. Khan, H.W. Koyro, B, Huchzermeyer & K.N.
Watanabe (2013). The influence of genes regulating
transmembrane transport of Na+ on the salt resistance of Aeluropus
lagopoides. Functional Plant Biology 40(9):
860–871.
Ahsan, N., T. Donnart, M.Z. Nouri & S. Komatsu (2010).
Tissue-specific defense and thermo-adaptive mechanisms of soybean seedlings
under heat stress revealed by proteomic approach. Journal of Proteome
Research 9(8): 4189–4204.
Ali, R. (2005).
Field studies for the conservation and management of Point Calimere
Complex. Foundation for ecological research, advocacy and learning. A Report
for the Tamil Nadu Forest Department, 40 pp.
Arandhara,
S., S. Sathishkumar & N. Baskaran (2020).
Modelling the effect of covariates on the detectability and density of native
Blackbucks and invasive feral-horse using multiple covariate distance sampling
at Point Calimere Wildlife Sanctuary, Southern India.
Mammalian Biology 100(2): 173–186.
Arandhara,
S., S. Sathishkumar, S. Gupta & N. Baskaran
(2021). Influence of invasive Prosopis
juliflora on the distribution and ecology of
native blackbuck in protected areas of Tamil Nadu, India. European Journal
of Wildlife Research 67(3): 1–16.
Ashokkumar,
M., S. Swaminathan & R. Nagarajan (2021).
Grass species composition in tropical forest of southern India. Journal of
Threatened Taxa 13(12): 19702–19713. https://doi.org/10.11609/jott.7296.13.12.19702-19713
Auken,
O.W. (2009). Causes and consequences of
woody plant encroachment into western North American grasslands. Journal of
Environmental Management 90(10): 2931–2942.
Bardgett,
R.D., J.M. Bullock, S. Lavorel, P. Manning, U.
Schaffner, N. Ostle, M. Chomel,
G. Durigan, L. Fry, D. Johnson & J.M. Lavallee
(2021). Combatting global grassland
degradation. Nature Reviews Earth & Environment 2(10): 720–735.
Barton, H., G. Mutri, E. Hill, L. Farr & G. Barker (2018).
Use of grass seed resources c. 31 ka by modern humans at the Haua Fteah cave, northeast Libya.
Journal of Archaeological Science 99: 99–111.
Baskaran, N., K. Ramkumaran & G. Karthikeyan (2016).
Spatial and dietary overlap between blackbuck (Antilope
cervicapra) and feral horse (Equus caballus) at Point Calimere
Wildlife Sanctuary, southern India: Competition between native versus
introduced species. Mammalian Biology 81(3): 295–302.
Baskaran, N., S. Arandhara, S. Sathishkumar &
S. Gupta (2019). Assessing the changes in land
use and land cover by invasive species and its influence on native flora &
ungulates in selected protected areas of Tamil Nadu, India using GIS and remote
sensing. Technical report submitted to SERB, Government of India.
Boval,
M & R.M. Dixon (2012). The importance of
grasslands for animal production and other functions: A review on management
and methodological progress in the tropics. Animal 6(5): 748–762.
Bryson, C.T. & R. Carter
(2008). The significance of Cyperaceae as Weeds, pp. 15–102. In: Naczi,
R.F.C. & B.A. Ford (eds.). Sedges: Uses, Diversity, and Systematics of the
Cyperaceae, 1st ed. Missouri Botanical
Garden Press, 298 pp.
Cai, H., X. Yang & X. Xu
(2015). Human-induced grassland
degradation/restoration in the central Tibetan Plateau: the effects of
ecological protection and restoration projects. Ecological Engineering
83: 112–119.
De Jong, T.J. (1995).
Why fast-growing plants do not bother about defence. Oikos
74(3): 545–548.
Derner,
J.D. & R.H. Hart (2007). Grazing-induced
modifications to peak standing crop in northern mixed-grass prairie. Rangeland
Ecology & Management 60(3): 270–276.
Egoh,
B.N., J. Bengtsson, R. Lindborg, J.M. Bullock, A.P. Dixon & M. Rouget (2016). The
importance of grasslands in providing ecosystem services: opportunities for
poverty alleviation, pp. 421–441. In: Routledge handbook of ecosystem services,
Routledge.
Fischer, L.K., M. von der Lippe
& I. Kowarik (2013).
Urban grassland restoration: which plant traits make desired species successful
colonizers? Applied Vegetation Science 16(2): 272–285.
Frank, S.J.D., G.V. Gopi, K. Sankar & S.A. Hussain (2021).
Dry season resource selection among sympatric ungulates in a tropical coastal
landscape: implications for conservation and management. Tropical Ecology
62(3): 418–426.
Ganskopp,
D & D. Bohnert (2001).
Nutritional dynamics of 7 northern Great Basin grasses. Rangeland Ecology
& Management/Journal of Range Management Archives 54(6): 640–647.
Hacker, J.B. (1984).
Genetic variation in seed dormancy in Digitaria
milanjiana in relation to rainfall at the collection
site. Journal of Applied Ecology 21: 947–959.
Hagenah, N., H. Munkert, K. Gerhardt & H. Olff
(2008). Interacting effects of grass
height and herbivores on the establishment of an encroaching savanna shrub, pp.
189–202. In: Valk, A.K. (ed.). Herbaceous Plant
Ecology. Recent Advances in Plant Ecology. Springer, 367+VII pp. https://doi.org/10.1007/978-90-481-2798-6
Hao, Y. & Z. He (2019).
Effects of grazing patterns on grassland biomass and soil environments in
China: A meta-analysis. PloS One 14(4):
p.e0215223. https://doi.org/10.1371/journal.pone.0215223
Hermance,
J.F., D.J. Augustine & J.D. Derner (2015).
Quantifying characteristic growth dynamics in a semi-arid grassland ecosystem
by predicting short-term NDVI phenology from daily rainfall: a simple four
parameter coupled-reservoir model. International Journal of Remote Sensing
36(22): 5637–5663.
Hughes, L., M. Westoby & A.D. Johnson (1993).
Nutrient costs of vertebrate-and ant-dispersed fruits. Functional Ecology
54-62 pp.
Huijser,
P. & M. Schmid (2011). The control of
developmental phase transitions in plants. Development 138(19):
4117–4129.
Hussain, F. & M.J. Durrani (2009).
Nutritional evaluation of some forage plants from Harboi
rangeland, Kalat, Pakistan. Pakistan Journal of Botany 41(3): 1137–1154.
Islam, M.R., C.K. Saha, N.R. Sharkar, M. Jahilil & M. Hasanuzzamam
(2003). Effect of variety on proportion
of botanical fraction and nutritive value of different Napier grass (Pennisetum puporeum)
and relationship between botanical fraction and nutritive value. Asian-Australasian
Journal of Animal Sciences 16: 177–188.
Jhala,
Y.V. (1997). Seasonal effects on the
nutritional ecology of blackbuck Antelope cervicapra.
Journal of Applied Ecology 34(6): 1348–1358.
Jing, Z., J. Cheng, J. Su, Y.
Bai & J. Jin (2014).
Changes in plant community composition and soil properties under 3-decade
grazing exclusion in semiarid grassland. Ecological Engineering 64:
171–178.
Khan, M.A. & S. Gulzar
(2003). Light, salinity and temperature
effects on the seed germination of perennial grasses. American Journal of
Botany 90: 131–134.
Kunwar, A., R. Gaire, K.P. Pokharel, S. Baral
& T.B. Thapa (2016). Diet of the four-horned
antelope Tetracerus quadricornis
(De Blainville, 1816) in the Churia hills of Nepal. Journal
of Threatened Taxa 8(5): 8745–8755. https://doi.org/10.11609/jott.1818.8.5.8745-8755
Liu, L., S. Bestel,
J. Shi, Y. Song & X. Chen (2013).
Paleolithic human exploitation of plant foods during the last glacial maximum
in North China. Proceedings of the National Academy of Sciences 110(14):
5380–5385.
Maron,
J.L. & E. Crone (2006). Herbivory: effects on
plant abundance, distribution and population growth. Proceedings of the
Royal Society B: Biological Sciences 273(1601): 2575–2584.
Moore, L.M., W.K. Lauenroth, D.M. Bell & D.R. Schlaepfer
(2015). Soil water and temperature
explain canopy phenology and onset of spring in a semiarid steppe. Great
Plains Research 25(2): 121–138.
Morgan, J.A., W. Parton, J.D. Derner, T.G. Gilmanov & D.P.
Smith (2016). Importance of early season
conditions and grazing on carbon dioxide fluxes in Colorado shortgrass steppe. Rangeland
Ecology & Management 69(5): 342–350.
Morgan, J.W., J.M. Dwyer, J.N.
Price, S.M. Prober, S.A. Power, J. Firn, J.L. Moore,
G.M. Wardle, E.W. Seabloom, E.T. Borer & J.S Camac (2016). Species
origin affects the rate of response to inter-annual growing season
precipitation and nutrient addition in four Australian native grasslands. Journal
of Vegetation Science 27(6): 1164–1176.
Munson, S.M. & A.L. Long
(2017). Climate drives shifts in grass
reproductive phenology across the western USA. New Phytologist
213(4): 1945–1955.
Murugan,
R., I. Djukic, K. Keiblinger,
F. Zehetner, M. Bierbaumer,
S. Zechmeister-Bolternstern & R.G. Joergernsen (2019).
Spatial distribution of microbial biomass and residues across soil aggregate
fractions at different elevations in the Central Austrian Alps. Geoderma 339: 1–8.
O’Mara, F.P. (2012).
The role of grasslands in food security and climate change. Annals of Botany
110(6): 1263–1270.
Parton, W., J. Morgan, D. Smith,
S. Del Grosso, L. Prihodko, D. LeCain,
R. Kelly & S. Lutz (2012). Impact of
precipitation dynamics on net ecosystem productivity. Global Change Biology
18(3): 915–927.
Popay,
I. & R. Field (1996). Grazing animals as weed
control agents. Weed Technology 10(1): 217–231.
Post, A.K. & A.K. Knapp
(2020). The importance of extreme
rainfall events and their timing in a semi-arid grassland. Journal of
Ecology 108(6): 2431–2443.
Rangel, A.A., D.D. Rockemann, F.M. Hetrick & S.K. Samal
(1999). Identification of grass carp haemorrhage virus as a new genogroup of aquareovirus.
Journal of General Virology 80(9): 2399–2402.
Ravi, N. & N. Mohanan (2002).
Common Tropical and Sub-tropical Sedges and Grasses. Science Publishers,
Inc., Enfield, New Hampshire
Rojas-Sandoval, J. (2016).
Dactyloctenium aegyptium
(crowfoot grass). Invasive Species Compendium, 19321 pp.
Sawyer, H., F. Lindzey & D. McWhirter (2005).
Mule deer and pronghorn migration in western Wyoming. Wildlife Society
Bulletin 33(4): 1266–1273.
Shankar, N.B. & J.
Shashikala (2010). Diversity and structure
of fungal endophytes in some climbers and grass species of Malnad
region, Western Ghats, Southern India. Mycosphere
1(4): 265–274.
Shaw, R.B. (2008).
Grasses of Colorado. University Press of Colorado, Boulder, CO, 650 pp.
Sherry, R.A., X. Zhou, S. Gu,
J.A. Arnone III, D.W. Johnson, D.S. Schimel, P.S. Verburg,
L.L. Wallace & Y. Luo (2011). Changes in
duration of reproductive phases and lagged phenological response to
experimental climate warming. Plant Ecology & Diversity 4(1): 23–35.
Shiferaw,
H., T. Alamirew, S. Dzikiti,
W. Bewket, G. Zeleke &
U. Schaffner (2021). Water use of Prosopis juliflora and its impacts on catchment water budget and
rural livelihoods in Afar Region, Ethiopia. Scientific Reports 11(1):
1–14.
Sivaganesan,
N. (1991). The ecology of the Asian
Elephant in Mudumalai Wildlife Sanctuary, with
special reference to habitat utilization. Unpublished PhD Thesis. Bharathidasan
University, Tiruchirapalli.
Solofondranohatra,
C.L., M.S. Vorontsova, J. Hackel,
G. Besnard, S. Cable, J. Williams, V. Jeannoda & C.E. Lehmann (2018).
Grass functional traits differentiate forest and savanna in the Madagascar
central highlands. Frontiers in Ecology and Evolution 6: 184.
Treydte,
A.C., J.G. van der Beek, A.A. Perdok
& S.E. van Wieren (2011). Grazing ungulates select
for grasses growing beneath trees in African savannas. Mammalian Biology
76(3): 345–350.
Wan, C., I. Yilmaz & R.E. Sosebee (2002).
Seasonal soil-water availability influences snakeweed root dynamics. Journal
of Arid Environments 51: 255–264.
Wang, T., X. Jin,
Z. Chen, M. Megharaj & R. Naidu (2011).
Green synthesis of Fe nanoparticles using eucalyptus leaf extracts for
treatment of eutrophic wastewater. Science of the Total Environment 466:
210–213.
Wardle, J. (1971).
The forests and shrublands of the Seaward Kaikoura Range. New Zealand
Journal of Botany, 9: 269─292
White, R.P., S. Murray, M. Rohweder, S.D. Prince & K.M. Thompson (2000).
Grassland Ecosystems. World Resources Institute, Washington, DC, 81 pp.
Xu, W., X. Deng, B. Xu, J.A. Palta & Y. Chen (2021).
Soil Water Availability Changes in Amount and Timing Favor the Growth and
Competitiveness of Grass Than a Co-dominant Legume in Their Mixtures. Frontiers
in Plant Science 12: 723839.
Zeng, D.H., L.J. Li, Z.Y. Yu,
Z.P. Fan & R. Mao (2010). Soil microbial properties
under N and P additions in a semi-arid, sandy grassland. Biology and
Fertility of Soils 46(6): 653─658.
Zhang, Y., Q. Wang, Z. Wang, Y.
Yang & J. Li (2020). Impact of human
activities and climate change on the grassland dynamics under different regime
policies in the Mongolian Plateau. Science of the Total Environment 698:
134304.