Biological diversity is a modern contraction of the word biodiversity. Biological diversity, thus, refers to variation within the living world or within and among living species. Diversity is defined as the range of variation, variety, or differences among a collection of traits. Most often used to refer to the quantity of species, the term “Biodiversity” was originally coined by lovejoy (1980) in its extended for, biological diversity (Swingland, 2001). Amounts of biodiversity the complexity of life on earth is created by the interaction of the three levels of biodiversity that are examined here: (1) Genetic diversity, (2) Species diversity, (3) Ecosystem diversity. The present research focuses on species diversity through the systematic identification and documentation of plant and faunal species within the study area. It is the variation between species within a community or between species within a species population. The species is the actual fundamental unit of classification for organisms, and the most widely used level for characterizing biodiversity is its diversity. In general, it depicts the quantity and species richness of a population. Because of this, species are unique units of diversity, each of which contributes in a unique way to the environment (Ashok Verma, 2016).
Urbanization and Riverfront Transformation:
India’s urbanization has complicated the country’s landscape ecology and human society (Chaturvedi et al.,2013). The choice to turn eleven kilometers of the city’s monsoon river into a riverfront is one example of how Ahmedabad’s spatial shape has changed as a result of the city’s growing urbanization. With strong political backing for the “environmental improvement and urban rejuvenation project” The Sabarmati Riverfront project has a broad scope and ambitious goals (Dempsey et al.,2020). In order to promote environmental sustainability and conserve local flora and fauna diversity, several green spaces have been developed along the riverfront, including the Flowers Park, Biodiversity Park, Miyawaki Forest Patches, and multiple riverfront gardens at Usmanpura and Vasna, collectively enhancing the ecological value of the urban landscape (Paneria et al.,2017)
Fig 1: Zonation map of the Sabarmati Riverfront, Ahmedabad, showing parks, development areas, and river promenade. (Reference: Amirtahmasebi et al., 2016)
Study Area:
The Sabarmati Riverfront Biodiversity Park in Ahmedabad, Gujarat, India, is the site of the current study. An essential part of the Sabarmati Riverfront development, the biodiversity park aims to improve habitat, save endangered species and support urban ecological restoration. The Biodiversity Park is separated into two sections and covers an area of roughly 65,000 m². The current study was limited to Phase 1, which has a total area of about 20,000 m². Nearly 5,000 no. of plants, representing roughly 60 different plant species, make up Phase 1. A variety of attractive, native, and ecologically significant plant taxa make up the flora, adding to the heterogeneity of the system. Phase 2: There are around 100 plant species in Phase 2, which covers an area of about 45,000 m². Plantation operations have been finished in a number of areas, and the vegetation is presently establishing and maturing, even though this phase is not yet accessible to the general public. Important ecological and cultural species have been introduced, such as the Sandalwood (Santalum album) and Sindoor (Bixa Orellana). In several areas of Phase 2, development is still in progress.
Fig 2: Riverfront Biodiversity Park, Ahmedabad
Field investigation for the present research was initiated in Late November and continued through Early December. Dense forest cover and the biodiversity park’s proximity to the Sabarmati River have an impact on localized microclimatic conditions, even though the park is part of Ahmedabad’s larger semi-arid climate regime. Compared to nearby metropolitan region, increased canopy cover results in comparatively greater humidity levels, improved soil moisture retention, and reduced ambient temperatures. Together, these macro- and microclimatic elements affect the study area’s seasonal patterns of fungal emergence, faunal activity, and plant growth.
Materials and Methods:
The previously reported study site, which is situated along the Sabarmati Riverfront in Ahmedabad, Gujrat, India was the location of field experiments. Regular field visits were made on weekends (Saturday and Sunday) during the survey’s four-month duration, which ran from November to February. In order to optimize the detectability of flora and faunal activities, observations were mostly conducted in the morning between 07:00 AM and 11:00 AM. Throughout the research area, many and methodical field treks over various habitat patches were used to document the flora. During these surveys, every species of vascular plant that was found was closely examined, documented, and photographed in the field. Observable morphological characteristics, such as leaf arrangement, inflorescence type, floral structure, and growth habit, were used for preliminary identification. Standard regional taxonomic literature, such as Flora of Gujarat and Practical Botany (Bendre & Kumar, 2008), was used to authenticate the species. To preserve uniformity in systematic arrangement, the recognized scientific names and associated higher taxonomic placement were confirmed in line with the Bentham and Hooker classification system. Every verified species was listed and assembled into an extensive, methodically structured checklist that reflected the floristic makeup of the research location.
Observable morphological traits, growth from, and substrate association within the study area were used to systematically document fungal occurrences. Macroscopic characteristics such cap shape, pore or gill structure, texture, color, and pattern of attachment to the substrate were the main tools used for identification of specimens found during field survey. We meticulously documented the fungi’s growth pattern and ecological niche, including whether they were saprophytic on the surfaces of living plants, leaf litter, or rotting wood (Webster & Weber, 2007). Broader classification was established using distinctive traits that pointed to Ascomycetes and Basidiomycetes types. Approximately seven to eight morphologically different fungus kinds were identified during survey time. The growth of a Polyporous basidiomycetes on woody substrate was noteworthy. This specimen showed discernible chromatic variation, which was probably caused by the weather at the time. The documented specimen had a yellowish-green marginal tint, which may have been caused by seasonal change or moisture fluctuation. Normally, Polyporous mushrooms exhibit a whitish edge during active growth (Bendre & Kumar, 2021). These findings demonstrate how macrofungi’s morphological responses to the local microclimate at the research location are dynamic.
Fig 3: Polyporous fungi observed on decaying wood
Fig 4: Polyporous fungi with Yellowish green margin due to weathering effect
During field walks across various habitats and microhabitats within the study region, systematic visual encounter surveys were used to conduct faunal observations. The behavior and preferred habitats of visible wildlife, including insect, birds, and arachnids, were meticulously examined. In order to accurately describe morphological characteristics such body form, coloration, wing pattern, and distinctive traits, specimens were photographed in situ (Vala et al.,2020). Organisms were recognized to the highest feasible taxonomic level based on field features and a through morphological investigation. A systematic faunal inventory was then created by employing the proper scientific nomenclature and classification hierarchy to arrange and collate all confirmed taxa. Notably, three of India’s top five venomous snake species are known to exist in the research area. However, Russell’s viper was the sole poisonous species encountered during the current survey period (Whitaker et al.,2004). The snake was presumably displaced from its typical habitat into the wet region when the individual was spotted during a period of intense rainfall when the boardwalk was momentarily inundated by high river water level (Wolfgang et al.,1992).
Fig 5: Russell’s Viper observed swimming in floodwater during heavy rainfall.
In insects, the start of a molting cycle is neither purely periodic nor random. Given that molting can achieve many goals depending on the situation, such as changing size or shape, it makes sense to assume that the timing of a molt needs to be adjusted to accommodate these purposes. Because the initiation of metamorphosis ends a larva’s growth period and determines the adult insect’s body size, it is very important to carefully regulate the start of a metamorphic molt (Nijhout, 1981). Molting, or ecdysis, is a fundamental biological process not only in insect but across thr entire phylum Arthropoda. This physiological mechanism underpins the evolutionary success and diversification of arthropods. With almost a million species listed in the catalogue of the most species among Metazoa, making it a remarkable illustration of the animal kingdom’s variety and evolutionary success (Campli et al., 2024). The superphylum Ecdysozoa, which comprises all organisms that grow via ecdysis, or the molting of their exoskeletons (Daley et al., 2018), is where the arthropods originated more than 500 million years ago from their last common ancestor (Giribet and Edgecombe, 2019). During the survey, direct field evidence of ecdysis was recorded, including the photographic documentation of alive insect undergoing molting. These observations provided in situ confirmation of active development processes within the arthropod community of the study area.
Fig 6: Exoskeleton of an arthropod observed on the leaf surface, indicating recent molting
Fig 7: Long-legged fly observed undergoing molting on a leaf surface
RESULTS
The biodiversity assessment of the selected study area revealed a diverse assemblage of plant and animal species, reflecting the ecological richness of the site. 109 vascular plant species, representing a diverse variety of life forms and development behaviors, made up the floristic component. The presence of fungi, with only six species identified, most of which were basidiomycetes and found on decomposing organic matter. With 20 species identified in several orders, including insect and arachnids, the faunal inventory demonstrated a noteworthy diversity of arthropods. 22 chordate species (Ganpule et al., 2014), which constitute avifauna and a few terrestrial vertebrates, were found among vertebrates. Furthermore, the research area had lone representatives of less frequently observed invertebrate phyla, such as one species of each of the Mollusca and platyhelminthes, underscoring the park’s biological niches and microhabitat variety.
Table 1: Systematic Floristic inventory of vascular plant species recorded from the Sabarmati Riverfront Biodiversity Park, Ahmedabad, Gujarat
|
Sr. no. |
Scientific Name |
Family |
Common Name |
|
|
Annona squamosa L. |
Annonaceae |
Custard Apple |
|
|
Polyalthia longifolia (Sonn.) Thw. |
Annonaceae |
False Ashoka |
|
|
Cocculus hirsutus (L.) Theob. |
Menispermaceae |
Vevdi |
|
|
Tinospora cordifolia (Willd.) Miers ex Hook. f. & Thoms. |
Menispermaceae |
Giloy |
|
|
Adansonia digitata L. |
Malvaceae |
African Baobab |
|
|
Abutilon indicum (L.) Sweet, Hort. |
Malvaceae |
Indian Mallow |
|
|
Bombax ceiba L. |
Malvaceae |
Red Silk Cotton |
|
|
Hibiscus rosa-sinensis L. |
Malvaceae |
Gurhal |
|
|
Hibiscus tiliaceus L. |
Malvaceae |
Sea Hibiscus |
|
|
Sterculia foetida L. |
Malvaceae |
Wild Indian Almond |
|
|
Thespesia populnea (L.) Soland. ex. Corr. |
Malvaceae |
Indian Tulip Tree |
|
|
Aegle marmelos (L.) Corr. |
Rutaceae |
Bael |
|
|
Citrus limon (L.) Burm. f. |
Rutaceae |
Lemon |
|
|
Murraya koenigii (L.) Spreng. |
Rutaceae |
Curry Leaf Tree |
|
|
Azadirachta indica A. Juss. |
Meliaceae |
Neem |
|
|
Khaya senegalensis (Desr.) A.Juss. |
Meliaceae |
Khaya |
|
|
Moringa oleifera Lam. |
Moringaceae |
Drumstick |
|
|
Sapindus mukorossi Gaertn. |
Sapindaceae |
Indian Soap Berry |
|
|
Ziziphus mauritiana Lam. |
Rhamnaceae |
Ber, Indian Jujube |
|
|
Mangifera indica L. |
Anacardiaceae |
Mango |
|
|
Abrus precatorius L. |
Fabaceae |
Rosary Pea, Chanothi |
|
|
Butea monosperma (Lam.) Taub. |
Fabaceae |
Palash |
|
|
Dalbergia sissoo Roxb. |
Fabaceae |
Shisham |
|
|
Lablab purpureus (L.) Sweet |
Fabaceae |
Val |
|
|
Pongamia pinnata (L.) Pierre |
Fabaceae |
Karanj |
|
|
Bauhinia purpurea L. |
Fabaceae |
Kachnar |
|
|
Caesalpinia pulcherrima (L.) Sw. |
Fabaceae |
Orange Galtoro |
|
|
Caesalpinia pulcherrima F. flava |
Fabaceae |
Yellow Galtoro |
|
|
Cassia fistula L. |
Fabaceae |
Golden Shower Tree |
|
|
Cassia javanica L. |
Fabaceae |
Pink Shower Tree |
|
|
Cassia siamea Lam. |
Fabaceae |
Kashid |
|
|
Delonix regia (Boj.) Raf. |
Fabaceae |
Gulmohar |
|
|
Peltophorum pterocarpum (DC.) Backer ex K. Heyne |
Fabaceae |
Copperpod |
|
|
Acacia nilotica (L.) Del. Subsp. Indica (Bth.) Brenan |
Fabaceae |
Gum Arabic Tree |
|
|
Acacia auriculiformis A. Cunn. ex. Bth. |
Fabaceae |
Australian Babul |
|
|
Albizia lebbeck (L.) Bth. |
Fabaceae |
Shirish Tree |
|
|
Calliandra inaequilatera Rusby |
Fabaceae |
Powder Puff |
|
|
Pithecellobium dulce (Roxb.) Bth. |
Fabaceae |
Gorus Ambli |
|
|
Prosopis cineraria (L.) Druce |
Fabaceae |
Khejari, Khijdo |
|
|
Tamarindus indica L. |
Fabaceae |
Imli |
|
|
Prunus avium L. |
Rosaceae |
Wild Cherry |
|
|
Anogeissus acuminata (Roxb. ex DC.) Guill. |
Combretaceae |
Button Tree |
|
|
Conocarpus lancifolius Engl. |
Combretaceae |
Conocarpus |
|
|
Terminalia bellirica (Gaertn.) Roxb. |
Combretaceae |
Behda |
|
|
Terminalia catappa L. |
Combretaceae |
Indian Almond |
|
|
Terminalia arjuna (Roxb.) W. & A. |
Combretaceae |
Arjun Tree |
|
|
Callistemon citrinus (Curtis) Skells |
Myrtaceae |
Bottlebrush |
|
|
Eucalyptus globulus Labill. |
Myrtaceae |
Nilgiri |
|
|
Syzygium cumini (L.) Skeels |
Myrtaceae |
Jamun |
|
|
Lawsonia inermis L. |
Lythraceae |
Mehndi |
|
|
Couroupita guianensis Aubl. |
Lecythidaceae |
Cannon Ball Tree |
|
|
Polyscias scutellaria (Burm.f.) Fosberg |
Araliaceae |
Aralia |
|
|
Tarlmounia elliptica (DC.) H. Rob., S.C. Keeley, Skvarla & R.Chan |
Asteraceae |
Curtain Creeper |
|
|
Phoenix dactylifera L. |
Ericaceae |
Date Palm |
|
|
Washingtonia robusta H. Wendl. |
Ericaceae |
Mexican Fan Palm |
|
|
Manilkara zapota (L.) van Royen |
Sapotaceae |
Chikoo |
|
|
Madhuca longifolia (J. Koenig ex L.) J.F. Macbr |
Sapotaceae |
Mahua |
|
|
Manilkara hexandra (Roxb.) Dub. |
Sapotaceae |
Rayan |
|
|
Mimusops elengi L. |
Sapotaceae |
Borsalli |
|
|
Jasminum auriculatum Vahl |
Oleaceae |
Indian Jasmine |
|
|
Jasminum sambac (L.) W. Ait. |
Oleaceae |
Mogra |
|
|
Nyctanthes arbortristis L. |
Oleaceae |
Parijat |
|
|
Salvadora sp. |
Salvadoraceae |
Piludi, Peelu |
|
|
Allamanda cathartica L. var. hendersonii Bailey |
Apocynaceae |
Yellow Allamanda |
|
|
Carissa carandas L. |
Apocynaceae |
Karonda |
|
|
Cascabela thevetia (L.) Lippold |
Apocynaceae |
Yellow Karen |
|
|
Tabernaemontana divaricata (L.) R.Br. ex Roem. & Schult. |
Apocynaceae |
Chandani |
|
|
Thevetia peruviana Var. alba |
Apocynaceae |
White Karen |
|
|
Cordia monoica Roxb. |
Boraginaceae |
Gunda |
|
|
Cordia dichotoma Forst. f. |
Boraginaceae |
Gunda, Snot Berry |
|
|
Cordia sebestena L. |
Boraginaceae |
Geiger Tree |
|
|
Jacquemontia pentanthos (Jacq.) G.Don |
Convolvulaceae |
Cluster vine |
|
|
Cestrum nocturnum L. |
Solanaceae |
Night Jasmine |
|
|
Asystasia gangetica (L.) T. Anders. |
Acanthaceae |
Coromandel |
|
|
Barleria cristata L. |
Acanthaceae |
Vajradanti |
|
|
Thunbergia erecta Var. Alba |
Acanthaceae |
White Bush Clock vine |
|
|
Thunbergia erecta (Benth.) T.Anderson |
Acanthaceae |
Bush Clock vine |
|
|
Kigelia pinnata (Jacq.) DC. |
Bignoniaceae |
Sausage Tree |
|
|
Millingtonia hortensis L. f. |
Bignoniaceae |
Indian Cork Tree |
|
|
Spathodea campanulata Beauv. |
Bignoniaceae |
African Tulip Tree |
|
|
Tabebuia rosea (Bertol.) DC. Prodr |
Bignoniaceae |
Pink Trumpet Tree |
|
|
Tecoma gaudichaudi DC. |
Bignoniaceae |
Yellow Bell Flower |
|
|
Lantana camara L. var. aculeata (L.) Mold. |
Verbenaceae |
Wild sage |
|
|
Vitex negundo L. |
Lamiaceae |
Nagod |
|
|
Clerodendrum inerme (L.) Gaertn. |
Lamiaceae |
Wild jasmine |
|
|
Grevillea robusta Cunn. ex R. Br. |
Proteaceae |
Silver Oak |
|
|
Achyranthes aspera L. var. aspera |
Amaranthaceae |
Anghedi |
|
|
Alternanthera sessilis (L.) Dc. |
Amaranthaceae |
Sessile Joyweed |
|
|
Coccoloba uvifera (L.) L. |
Polygonaceae |
Sea grape |
|
|
Bougainvillea spectabilis Willd. |
Nyctaginaceae |
Bougainvillea |
|
|
Jatropha integerrima Jacq. |
Euphorbiaceae |
Jatropha |
|
|
Phyllanthus emblica L. |
Euphorbiaceae |
Amla |
|
|
Putranjiva roxburghii Wall. |
Euphorbiaceae |
Putranjiva |
|
|
Holoptelea integrifolia (Roxb.) Planch |
Ulmaceae |
Indian Elm |
|
|
Ficus virens Ait. |
Moraceae |
Pilkhan |
|
|
Ficus racemosa L. |
Moraceae |
Cluster fig, Umbro |
|
|
Ficus benghalensis L. |
Moraceae |
Banyan Tree |
|
|
Ficus lyrata Warb. |
Moraceae |
Fiddle-leaf Fig |
|
|
Ficus religiosa L. |
Moraceae |
Peepal |
|
|
Morus alba L. |
Moraceae |
Mulberry |
|
|
Cycas revoluta Thunb. |
Cycadaceae |
Cycas |
|
|
Agave americana L. var. marginata |
Amaryllidaceae |
Century Plant |
|
|
Dioscorea bulbifera L. |
Dioscoreaceae |
Air Potato |
|
|
Canna indica L. |
Cannaceae |
Canna |
|
|
Cordyline fruticosa (L.) A.Chev. |
Liliaceae |
Red Dracena |
|
|
Dieffenbachia seguine (Jacq.) Schott |
Araceae |
Dumb Cane |
|
|
Bambusa vulgaris Schrad. ex J.C. Wendl. |
Poaceae |
Golden Bamboo |
|
|
Cynodon dactylon (L.) Pers. |
Poaceae |
Durva |
|
|
Dendrocalamus calostachys (Kurz) Kurz |
Poaceae |
Green Bamboo |
Table 2: Inventory of macrofungal species recorded during the survey in the Sabarmati Riverfront Biodiversity Park, Ahmedabad, Gujarat.
|
|
Daldinia concentrica (Bolton) Ces. & De Not. |
Hypoxylaceae |
Coal Balls Fungi |
|
|
Lentinus squarrosulus (Mont.) |
Polyporaceae |
White Shiitake |
|
|
Marasmiellus Candidus (Fr.) |
Omphalotaceae |
Snow Fungi |
|
|
Schizophyllum commune Fr. |
Schizophyllaceae |
Split Gill Mushroom |
|
|
Trametes versicolor (L.) Lloyd |
Polyporaceae |
Ployporous |
|
|
Tubaria furfuracea (Pers.) Gillet |
Tubariaceae |
Scurfy Twiglet |
Table 3: Inventory of arthropod fauna recorded from the Sabarmati Riverfront Biodiversity Park, Ahmedabad, Gujarat.
|
|
Anthia sexguttata (Fabricius) |
Carabidae |
Six Spot ground beetle |
|
|
Aulacophora foveicollis (Lucas) |
Chrysomelidae |
Red Beetle |
|
|
Brachythemis contaminata (Fabricius) |
Libellulidae |
Ditch Jewel |
|
|
Condylostylus sp. |
Dolichopodidae |
Long legged Fly |
|
|
Coridius ianus (Fabricius) |
Dinidoridae |
Red Pumpkin Bug |
|
|
Episyrphus balteatus (De Geer) |
Syrphidae |
Hover Fly |
|
|
Estigmene acrea (Dury) |
Erebidae |
Salt Marsh Caterpillar |
|
|
Graphium doson C. & R. Felder |
Papilionidae |
Jay Butterfly |
|
|
Halyomorpha halys Carl S. |
Pentatomidae |
Marmorated Stink Bug |
|
|
Musca domestica L. |
Muscidae |
Housefly |
|
|
Neoscona oaxacensis (Keyserling) |
Araneidae |
Zig Zag Spider |
|
|
Olene mendosa (Jacob Hübner) |
Erebidae |
Hairy tussock moth |
|
|
Paratrechina longicornis (Latreille) |
Formicidae |
Long Horn Crazy Ant |
|
|
Pholcus phalangioides (Fuesslin) |
Pholcidae |
Cellar spider |
|
|
Promachus sp. |
Asilidae |
Robber Fly |
|
|
Riptortus pedestris (Fabricius) |
Alydidae |
Broad Headed Bug |
|
|
Suastus gremius (Fabricius) |
Hesperiidae |
Palm Bob |
|
|
Tettigonia viridissima L. |
Tettigoniidae |
Great Bush Cricket |
|
|
Tetragnatha extensa L. |
Tetragnathidae |
Stretch Spider |
|
|
Tholymis tillarga (Fabricius) |
Libellulidae |
Evening skimmer |
Table 4: Inventory of chordate species recorded from the Sabarmati Riverfront Biodiversity Park, Ahmedabad, Gujarat.
|
|
Acridotheres ginginianus (Latham) |
Sturnidae |
Common Bank Myna |
|
|
Acridotheres tristis L. |
Sturnidae |
Common Myna |
|
|
Alcedo atthis L. |
Alcedinidae |
Kingfisher |
|
|
Argya caudata (Dumont) |
Leiothrichidae |
Babbler |
|
|
Athene blewitti (Hume) |
Strigidae |
Spotted Owlet |
|
|
Centropus sinensis (Stephens) |
Cuculidae |
Greater Coucal |
|
|
Cinnyris asiaticus (Latham) |
Nectariniidae |
Purple sunbird |
|
|
Columba livia (Gmelin) |
Columbidae |
Pigeon |
|
|
Corvus splendens (Vieillot) |
Corvidae |
House Crow |
|
|
Daboia russelii (Shaw & Nodder) |
Viperidae |
Russell’s viper |
|
|
Eudynamys scolopaceus L. |
Cuculidae |
Asian koel |
|
|
Lampropholis delicata De Vis. |
Scincidae |
Garden Skink |
|
|
Lonchura malacca L. |
Estrildidae |
Tricoloured Munia |
|
|
Merops orientalis (Latham) |
Meropidae |
Green Bee-eater |
|
|
Milvus migrans (Boddaert) |
Accipitridae |
Black kite |
|
|
Orthotomus sutorius (Pennant) |
Cisticolidae |
Tailor Bird |
|
|
Oriolus kundoo (Sykes) |
Oriolidae |
Golden Oriole |
|
|
Pavo cristatus L. |
Phasianidae |
Indian Peafowl |
|
|
Ptyas mucosa L. |
Colubridae |
Indian Rat Snake |
|
|
Psittacula krameri (Scopoli) |
Psittaculidae |
Parakeet |
|
|
Tyto javanica (Gmelin) |
Tytonidae |
Barn Owl |
|
|
Varanus bengalensis (Daudin) |
Varanidae |
Indian Moniter Lizard |
Table 5: Inventory of Platyhelminthes fauna recorded from the Sabarmati Riverfront Biodiversity Park, Ahmedabad, Gujarat.
|
1. |
Bipalium javanum (Loman) |
Geoplanidae |
Hammer Head Worm |
Table 6: Inventory of Mollusca recorded from the Sabarmati Riverfront Biodiversity Park, Ahmedabad, Gujarat.
|
1. |
Oxychilus draparnaudi (Beck) |
Oxychilidae |
Glass snail |
The systematic inventory of the Sabarmati Riverfront Biodiversity Park reveals a rich taxonomical composition, encompassing a total of 109 plant species, 6 fungal species, 44 faunal species. The vegetative structure of the park is predominantly arboreal, as illustrated in the distribution of plant species according to habits. Tree constitute the largest segment of the flora at 61%, followed by shrubs at 22%. This dominance of tree species indicates a well-established canopy layer, essential for urban microclimate regulation. Other growth forms, including herbs 7%, climber 7%, and grasses 3% contribute to the vertical stratification and ground cover of the ecosystem, supporting a diverse range of ecological niches (Bendre & Kumar, 2021). Concurrently, the Distribution of Fauna Species According to Groups shows that both lower and higher vertebrates and invertebrates are significantly present. At 41%, Aves are the most varied faunal category (Ganpule et al., 2014). Insects come in second at 39%. The park's floral environment appears to have a good supply of food supplies and nesting locations, as indicated by the wide diversity of birds and insects. Reptiles (9%) (Whitaker et al., 2004), Arachnids (7%), Mollusca (2%), and Platyhelminthes (2%) are further documented groups. Together, these results highlight the park's essential function as a hub for urban biodiversity, promoting intricate relationships between species and sustaining a robust ecosystem in an area that has been altered by human activity
DISCUSSION:
The current study shows that a physically and functionally integrated urban ecosystem with significant species richness is maintained in the Sabarmati Riverfront Biodiversity Park. A managed urban landscape has significant floristic variability, as evidenced by the recording of 109 vascular plant species. By improving primary productivity, habitat stratification, and structural complexity, such plant diversity establishes ecological niches that sustain a variety of trophic levels. In semi-arid urban settings, faunal assemblages depend on vertical layering and microclimatic buffering, which are facilitated by variation in life form such as tree, shrubs, climbers, herbs. The presence of six fungi species, which are primarily linked to organic substrates that are breaking down, indicates that there are active detrital routes in the park. As decomposers, fungi play crucial ecological roles by promoting the turnover of organic matter and the mineralization of nutrients (Gessner et al., 2010). Their existence is indicative of continuous biogeochemical cycling mechanism that maintain plant regeneration and soil fertility. Environmental responsiveness and adaptive morphological plasticity within the mycobiota are further suggested by the observation of a Polyporous basidiomycetes displaying margin color fluctuation under changed moisture conditions. These characteristics highlight how susceptible fungal communities are to change in the microclimate, especially in riparian urban environments.
The site’s trophic interconnectivity is highlighted by the faunal inventory, which includes 22 chordate species and 20 arthropod species. Arthropods are the link between primary producers and higher vertebrates, acting as primary consumers, pollinators, decomposers, and prey organisms (Schowalter et al., 2018). The variety of insects and arachnids seen in different habitat patches suggests that functional guilds, including herbivorous, predatory, and shelter are call reflected in avifaunal and other chordate records, which together indicate habitat appropriateness in an environment that has been anthropogenically altered. Despite their small numbers, the discovery of Platyhelminthes and Mollusca representatives highlights the landscape’s moisture-dependent niches and microhabitat variability. Crucially, biological confirmation of ongoing developmental cycles within the arthropod community is provided by direct field evidence of ecdysis, such as exuviae from shed spiders and an insect going through molting (Truman & Riddiford, 2002). In molting creatures, molting is a physiological process that is hormonally controlled and necessary for growth and metamorphic transformation. Its presence in situ suggests that the habitat promotes effective growth and life cycle completion in addition to supporting transient individuals. These findings support the ecological understanding of the location as a working system as opposed to just a decorative green area (Riddiford, 2012).
Primary production, decomposition, trophic transfer, and developmental succession are among the interconnected ecological process that are demonstrated by the integration of floristic, mycological and faunal components. The ability of planned green areas to preserve aspects of natural ecosystem dynamics is demonstrated by the coexistence of several taxonomic group inside an urban riverside matrix (Loreau et al., 2001). The inventory creates a fundamental basis for long term biodiversity monitoring and ecological assessment, albeit being a temporal snapshot limited to the survey period. Systematically documented inventory like this one help us better understand how managed landscapes can support biological diversity in the face of growing urban expansion. The study emphasizes how urban biodiversity parks can serve as havens that support species survival, ecological interactions, and developmental continuity in urban settings provided they are structurally varied and ecologically maintained.
CONCLUSION
A through examination of the Sabarmati Riverfront Biodiversity Park showed that it was covered to 109 vascular plant, 6 fungi, 20 arthropods, 22 chordates, and representative of Mollusca and Platyhelminthes. Together, these species enable food web interactions, habitat variability, and nutrient cycling, which all contribute to the structure and functionality of the urban ecosystem. The ecosystem’s continuous biological dynamics are highlighted by observation of active developmental process, such as the incomplete documenting of bug and spider molting. A baseline for comprehending ecosystem change is provided by this combined floristic and faunal inventory, which is also a vital resource for upcoming biodiversity monitoring, conservation, and sustainable management plans.
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Bhavna Singh*
Shiv Gupta
10.5281/zenodo.19662730