Thursday, 25 April 2019

Depression : trap of emotional infidelity



Depression???

Dr. Asma Ali ( Ecologist)

Just a day before, I was planning to write a blog on depression and this morning when I was thoroughly reading headlines (certainly... headlines) on newspaper I picked up a news where a TV actress Renee Dhyani open up one of the toughest phase of her life that she has been battling depression for almost a year after her heartbreak. Some times common people like us plunge into the fantasy world where we get trap with illusion that celebrities have everything in their life (does everything refers money, fame, lavish lifestyle, fan following, bodyguard) ; then why do celebrities despite having everything get into depression?




The answer had to be a bit long this time and I need just few quality minutes of your life to spark a change on the way you look at life, forever.

If we take a look deep down within ourselves and ask “What is the most desirable thing of our life?”. I am sure answer will not be so different for all of us IT'S  HAPPINESS. So close your eyes and think about the happiest moment of your life, most likely some of the memories of your childhood will flash right before you or the days of your college canteen or library and the days when your career was on the peak, the days when you blessed with baby and that would be your HAPPY SLIDE SHOW COLLECTION.

Those days when you cherished feeling the breeze in the warmth of the Sun and there was nothing in life that bothered you ( healthy competition with cronies and not politics for sure) we really wanna go back to those days when we were stupid, less equipped but HAPPY.

Being a center of attraction celebrities don't have freedom to move freely, they use to handle stage and public appearance that leave constant stress and anxiety on them. There is a tough competition in every field but celebrities are living in quite complex niche, they require to give their 100% every time, they have to work hard to keep their feet on industry. Name, fame, Life style ; all these things are not permanent and there is always a fear of losing them (synthetic life is eating up the world). Recently Deepika Padukone also address her depression candidly. Some of the celebrities have spoken about their reason of depression while some have not. Some of the hidden reasons maybe past trauma, drug abuse, anxiety etc.


                       Here are some examples of celebrities who went under depression like George Michael sheer superstar who wanted to live his life and steer his career his way, lost his lover Anselmo Feleppa back in 95; he grieved for so long and the song JESUS TO A CHILD was the outcome.

                          Another famous celebrity Oprah Winfrey opened up her suicide thought in an interview. When we talk about Indian stars like Hrithik Roshan who was afflicted to depression after making couple of flop movie; Ileana D'Cruz has been with anxiety, body dysmorphic disorder and depression for almost 15 years and Sanjay Dutt battled with depression when he was Re-imprison in 2013. He was unable to sleep during his jail term.


                         PERFECTION AND EXPECTATION  are found to be adequate tools of depression. When you expect a lot from your surrounding people or the person you are attached most, lead you to shatter your soul into pieces ; where you allow a person to be a driving force of yours smile, your happiness. Let me focus on second point…...PERFECTION; no one in this world is perfect, then how could you expect perfect performance from oneself, or we use to pretend as a perfect in this and that….

                                  Life is a thin thread it takes a second to snap... the CREATURE OF UNIVERSE blessed each and everyone of us with uniqueness….. never give up.



(continue………..)


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Tuesday, 23 April 2019

plant insect interaction

Influence of host plant diversity on the survival and abundance of certain shoreline insects of a tropical lake of Bhopal,  India.

 Dr. Asma Ali (Ecologist)


 ABSTRACT: (1) Plant-insect interaction is a vital component of community structure in any aquatic ecology, particularly with respect to predation, competition and resource spiraling. Availability of aquatic plants can potentially influence every aspect of the life of marginal invertebrate communities of lakes, such as their life cycle, choice of habitat and behavior.

(2) To investigate the importance of host plant diversity for marginal insects of a fresh water body called as Upper Lake, Bhopal, India, population densities of the marginal insects of order, Hemiptera, Coleoptera, Odonata, Orthoptera, Diptera and Strepsiptera were recorded during two years of study period, at four different sampling stations of the large man made tropical Lake.


(3) The data of the study suggest that, most of the insect species had significantly higher survival rate when they were feeding on several host plants, as compared to those, who fed on specific plant species. In the present study it was observed that an increase of plant matter in a subsurface ecosystem indicated significantly high abundance and diversity of aquatic as well as terrestrial insect population.


(4) The present data also demonstrate that loss of shoreline vegetations may reduce the productivity of both aquatic and terrestrial insects, possibly by adversely affecting the amount of allochthonous material entering the shoreline along with microclimate conditions. Although data on plant quality were not available in this study, population data were analyzed to determine the effect and interrelationship of plant insect population growth.


Key words: Plant-insects interactions, shoreline vegetations, insect’s communities, host plant, population abundance and diversity.  


1. INTRODUCTION:

In recent years, there has been a considerable interest in how aquatic species diversity influences ecosystem functions. Various experimental designs have been used to investigate this question in laboratory micro and meso-cosms as well as in field plots with different numbers of plant species (Hector et al., 1999, Boyero 2002, Briers and Biggs 2005) in which diversity has been manipulated at a variety of trophic levels. Consequently the trophic ecology of aquatic invertebrates has received considerable attention from stream ecologists, however in temperate regions of the Northern Hemisphere (Hynes 1970, Merrit and Cummins 1984, Carehino et al. 2003) and to a lesser extent, the Southern Hemisphere (Chessman 1986, Yule, 1996, Death & Zimmermann 2005, Clarke et al. 2008). On the other hand such species diversity influences and their trophic significance in tropical large water bodies are wanting.

Shoreline insects in relation to shoreline macro-vegetations in the ecotone between the lake and land. Such transitional habitats are often ignored because of the different background of aquatic and terrestrial ecologist. However, these ecotones are important for species and process that encounter them as boundaries. Thus the equally challenging and interesting area compelled us to undertake the present study where macrophytes and other shoreline vegetations and their population abundance in relation to the certain shoreline insect’s growth are very interesting and indicating the rich potential with dense vegetation zone. It has been attempted to document an association between both less vegetated and dense vegetated shoreline zones and their associated shoreline insect fauna in one of the largest man made tropical lakes of central India called as Upper Lake. The purpose of the study was firstly to determine the presence of supralittoral vegetation, affecting the diversity and composition of insect communities in shoreline ecotone and secondly to identify the nature of such associations between the vegetation and insect communities.
 
2. MATERIAL AND METHODS:

 2.1 Description of study area:

The Upper Lake is located in Bhopal city, the capital of Madhya Pradesh, the largest state of India. Constructed on earthen dam across the river Kolans in the 11th century created this lake, the Upper Lake has water spread area of 30.72 sq.km at FTL. The storage capacity is 101.6 million cu.m, the maximum and mean depth being 11.7 and 6 m. respectively. The Upper Lake is under a massive conservation, restoration and management project funded by Overseas Economic Cooperative Fund (OECF) Japan to protect it from environmental degradation not only due to its natural aesthetic value and rich biodiversity, but also since it is the main source of potable water.
Selection of the sampling sites of the Upper Lake chiefly was done on the basis of weeds and consequent biomass sampling. Sampling was done at four sampling sites of Upper Lake viz. Bhadbhada, Van-vihar (National Park), Pump-house and Bairagarh designated as SI, SII, SIII and SIV. Among all the sampling stations, Van-vihar (SII) and Bairagarh (SIV) have dense vegetated shoreline habitats, whereas Bhadbhada weir (SI) is generally more disturbed than other three sampling sites, primarily because of its use as a camping site.
Upper Lake is divided into perennial water, covered, marshy and submerged cum dry zones .Due to shallow nature of the last zone the lake becomes exposed from post monsoon period to summer season, therefore the Lake supports mainly three types of vegetations consisting of more than 100 terrestrial or marshy plants and 34 aquatic plant species. The aquatic species have been categorized as floating, submerged and emergent forms. Selection of the sampling sites of the Upper Lake chiefly was done on the basis of weeds and consequent biomass sampling.

2.2. Sampling of marginal insects:

To investigate the species richness and abundance of marginal hemipteran insects as well as their plant interaction a belt quadrate method (Dicks et al., 2003) was applied to the transects. The quadrates were used at the start to the end of the sampling season. Sampling stations were studied for insects in each season i.e. summer, winter and rainy. Sampling walks started between 10 to 12 am, the period of relatively high visitation by insects in the order Hemiptera were collected, and after each sampling, one specimen of each species was brought back to the laboratory to confirm identification using standard texts.
The size, number and distribution of samples to be taken in an area was decided upon before hand in order to make sure that the sampling is representative typifying the study area as a whole. The quadrates used for sampling, must be of such dimensions that all the species, which occur in that community is fully represented.


2.3. Water analysis:

Sampling for water quality parameters and aquatic insects were carrying out at monthly intervals, covering dry and rainy seasons. Air and water temperatures were recorded with a thermometer, whereas pH, total alkalinity, dissolved oxygen, total hardness, calcium hardness and nutrients were determined according to APHA (2003) methods. Monthly rainfall, humidity and ambient temperature data were obtained from the meteorological station Bhopal, India.

2.4. Collection and Identification of macrophytes:

As primary producers, macrophytes represent an important food resource, and they also play a significant role in the oxygen balance and nutrient cycle of many watercourses. In view of their varying requirements, the composition of macrophyte species in a water body makes it possible to draw conclusions about the local chemical and physical conditions. Species that prefer low nutrient concentrations, in particular, have become much less prevalent. Also in decline are species that are dependent on natural riverbanks with sandy and gravelly substrates. Aquatic plants are especially sensitive to changes (increases) in nutrient concentrations (notably phosphorus and ammonium) and to organic pollutants. Samples of shoreline macrophytes were collected from different types of habitat like lake margin and identified by his guidelines given by Needham and Needham (1962) and Haslam (1978).

2.5.Statistical analysis:

The data were analyzed by SPSS (Statistical Package for Social Services Version 10). Descriptive statistics such as probability, frequency, percentage and mean values were used.
 
RESULTS:
During the ecological analysis of the Upper Lake in relation to diversity of insects group and shoreline vegetations in the present study, interesting observations have been made .At all the sampling stations of Upper Lake 35 plant species have been found to be present in varying numbers .Out of these species 15 dominant plant species such as Ipomoea aquatica, Ipomoea fistulosa, Ceratophyllum demersum, Hydrilla verticillata ,Najas minor, Potamogeton pectinatus, Potamogeton crispus, Potamogeton nodusus ,Eichhornia crassipes, Leersia hexandra, Azolla pinnata, Lemna minor, Utricularia flexuosa and Alternanthera were conspicuous throughout the study period and remaining plant  species such as Ageratum conyxoides, Kirgenalia reticulata, Trapa bispinosa and Cyperrus torundus were observed as a sub-dominant or rare species.
Shoreline vegetations of Upper Lake has been divided on the basis of their occurrence i.e. emergent, submerged, rooted and free floating forms, where Stations II and IV had a dence shoreline vegetations as compare to station I and III. Interestingly approximately 83 species of shoreline insects belonging to different orders were recorded in varying population numbers, ranging from 0.6 to14.6 sps/m² throughout the study period. Out of these insects species five insects orders were found to be present dominantly such as Coleoptera, Hemiptera, Odonata, Orthoptera and Lepidoptera. According to their dominance ,the station wise order has been found to be SII >SIV > SIII >SI. Seasonally it was observed that maximum vegetation was present during summer (18 to 70 species /20 m²) and rainy (10 to 52 species/20m²) seasons, whereas winter season had less dense population (8 to 46 species/20 m²) abundance of shoreline vegetations (Table 1).

         

                     

  The relationship between marginal insects and macrophytes were observed significantly positive for Ipomoea aquatic and Ipomoea fistulosa (P<0.001, r =0.89), Potamogeton pectinatus (P <0.001, r =0.90), Eichhornia crassipes (P < 0.001, r =0.90) for sub-merged, rooted macrophyte with porvopotamidae growth form, such as Hydrilla verticillata (P < 0.001, r = 0.90) and for common shoreline macrophyte, Leersia hexandra (P< 0.001, r =0.89). Two macrophyte species of Ipomoea, such as Ipomoea aquatica and Ipomoea fistulosa, three species of Potamogeton such as P. pectinatus, P. crispus, P. nodosus and the member of Pontedriaceae such as Eichhornia crassipes constituted 36.5±2.7, 29.5±2.4 and 23.9±2.7% respectively of total abundant vegetation during the study period.

In the present investigation it was observed that all three species of Potamogeton were found abundantly at station II (40 to 68 species/20m²) and IV (30 to 70 species /20 m²) and were observed less abundant at stations I and III being 10 to 20 species /20m². Interestingly it was also observed that some species of shoreline Coleopterans such as Dineutus indicus,Dineutus unidentatus and Colymbetus fuscus inhabitated on Potamogeton pectinatus, therefore  at stations II and IV these Coleopterans were recorded in maximum population density (32 to 46 species/20m²) as compared to stations I and III(18 to 28 species/20m²Table 1)






                       
               
      Eichhornia crassipes was a dominant macrophyte belongs to family Pontedriaceae, germinates after onset of rains, with high temperature range (30-32ºC) and also good nutrients and soft mud of the littoral zone provided a favorable growth of E. crassipes. Interestingly insect population densities on E. crassipes were found to be significantly higher than on all other plant species. Most of the Dipterans (Culiseta longiareolata, Dolicocephala irrorata, Syrphus vitripennis) some Odonatens (Lestes orientalis, Ischnaru elegans, Libellula quadrimaculata) Coleopterans (Colymbetes fuscus, Dineutatus indicus, Dineutus unidentatus) and Hemipterans (Belostoma indicum, Corixa varicunda, Aradus acutus) were recorded maximum upon E. crassipes because of its high presence during most part of the year, in all sampling stations of Upper Lake (Fig.2). 

On an average analysis of the three seasons, it was observed that maximum number of dominant shoreline vegetation was recorded in summer because of the fact that light strikes in the Lake surface more directly in summer, than in winter, permitting greater light penetration, which was more favorable for the growth of this type of aquatic vegetation. Consequently maximum (18 to 70 species/20m²) shoreline insects of Upper Lake were also observed in summer season, optimum temperature was found to induce the growth and development of insects coupled with the dense population of shoreline vegetation gave support, shelter, food and breeding place to shoreline insects, making a positive symbiotic influence of vegetation as well as insect population (Table 2).

DISCUSSION:

For insects that feed on plants, variations in plant quality can have a profound effect on both levels of competition and mortality from natural enemies (Lill et al. 2002, Helms et al., 2004). Moreover, insects, by comparison with plants, have more specific other needs, such as for food, mating, nesting or oviposition and avoidance of death. Removal of shoreline vegetations may have cascading effects on both the aquatic and terrestrial components of the shoreline ecotone. There is increasing evidence that altering freshwater transitional ecotones affects the structure and function of the aquatic ecosystem they border .For example, reductions in leaf litter have been shown to limit the abundance of detritivores, thereby reducing population size of both aquatic and terrestrial insect prey available for fresh water fish.

In the present study it was observed that several aquatic macrophytes such as Eichhornia crassipes, Leersia hexandra and Potamogeton pectinatus confined themselves to shallow euphotic zones of the Upper Lake, which provided shelter to a large number of insects such as Belostoma indicum, Dineutus indicus, Dineutus unidentatus and Colymbetus fuscus Similarly riparian vegetation provided temperature and micro-climate, habitat complexity and prey refuges which increased the abundance of food and nutrient inputs as well Clear cutting of vegetations at Upper Lake margins altered the composition  of these invertebrates communities through changes in either food choice and habitat. Riparian vegetation provided temperature and micro-climate, habitat.
Across all taxa, Arthropods included several insects, their richness and abundance was higher in the dense vegetated site (stations II and IV) than at the less vegetated sites (stations I and III) of Upper Lake shorelines. Shoreline insects of Upper Lake were several times more abundant on an average at the dense vegetated sites as opposed to the less vegetated sites.
         This suggested that shoreline vegetations provided important functions for both aquatic and terrestrial insects associated with the marginal ecotone. Although the extent of association varied with different macrophytes within different season, at the same station and also between different stations for all the orders of insects found in the present study. These variations between insects and their host plants, was mainly due to the changes in food and shelter requirements, fish predation and the life cycle of individual groups.
                                          Season wise high abundance of marginal insects of 18-70 species/20m² was recorded in summer due to high temperature, which ranged 28 to 36.4ºC. This single factor induced photosynthetic activities of marginal vegetations. There was another factor of high insect abundance in summer, which may be due to phloem sap of grasses and forbs, which is generally accepted to be more nutritious in summer. Current results are similar to the findings of Douglas (1993) and Giulio and Edwards (2003) who have reported that high temperature range of 30 to 35 species/20m² affects on vegetation’s phloem sap and make them more nutritious, this attractive abundance of insect population.
           
                  Several species of Hemiptera such as G.lacustris inhabited on free floating vegetations of E. crassipes, whereas C. varicunda and R. varipes were found to colonise on submerged macrophytes such as V. spiralis and H. verticillata. Another abundant Hemiptera of Upper Lake B. indicum was found to be lotic and lentic in habitat and were observed on submerged macrophytes, H verticillata. Similar pattern of Hemipteran abundance has also been observed by several earlier workers such as Hilsenhoff (1977), Merrit and Cummins (1984), Erman (1984), Dobson (1994) and recently by Clarke et al. (2008) who have reported that peak of population abundance of aquatic insects coincided with the density of higher aquatic vegetation. In the present investigation it has been observed that most of marginal insects were specialized to their host plants where as some species had variable host plants.
             An interesting observation regarding variability of vegetation was seen in present study that Heteropteran insect survival rate was found higher when they feed on variable plants as compared to those who feed on only specific plant species, i.e. N.maculata, T. tendipes, C. longiareolata, B. indicum, R. varipes and N. viridula had more than one species of host plants such as H. verticillata, V. spiralis, E. crassipes and L. hexandra and they showed high survival rate as well as high population abundance. These results are in fairly good corroboration with the findings of Hunter (2001), Helms et al. (2004), Death & Zimmermann (2005) and Barnett & Beisner (2007) who have reported that survival of aquatic insects was dependent on their feeding habits and variation in host plant abundance.
          As evident from the several reports it may be concluded that almost all insects species of Upper Lake are affected by the presence of shoreline macrophytes. In the present study it was also observed that an increase of plant matter in a subsurface ecosystem induced both the abundance and diversity of aquatic as well as terrestrial population. Much as terrestrial insects such as Nemobious fasciatus, Atractomorpha crenulata, Chorthippus paralleus, Nezara viridula and Grillotalpa africana were primary consumers of plant matter so do aquatic insects such as Notonecta maculata, Hydrometra stagnorum, Belostoma indicum, Dineutus indicus and Gerris lacustris accounted for a large amount of the break down of plant material in subsurface ecosystem.
 Ramanuk and Levings (2003) Bahuguna et al. (2004) and Gallego et al. (2010) also suggested that insects are much dependent on the presence and composition of vegetations. Our results suggest that loss of shoreline vegetation may reduce the productivity of both aquatic and terrestrial insects, possibly by adversely affecting the amount of allochthonous material entering the shoreline and microclimate conditions, thus lake vegetations considerably influences survival and abundance of shoreline insects.

REFERENCE:

Anderson, W.B. and G. A. Polis (1998): Marine subsidies of island communities in the Gulf of California: evidence from stable carbon and nitrogen isotopes, Oikos, 81: 75-80.

APHA (2003): Standard methods for examination of water and wastewater, 23rd ed. American Public Health Association, Washington DC, Pp. 1134.

Baber, M.J., Fleishman, E., Babbitt, K.J. and Tarr, T.L. (2004): The relationship between wetland hydroperiod and nestedness patterns in assemblages of larval amphibians and predatory macroinvertibrates. Oikos 107, 16-27.

Barnett, A. and Beisner, B.E. (2007): Zooplankton biodiversity and lake trophic state: explanations invoking resource abundance and distribution Ecology 88, 1674-1686.

Bahuguna, B.K.; R. Nautiyal, P. Nautiyal and H.R. Singh (2004): Stream regulation: variations in the density, composition and diversity of benthic macro-invertibrates occurring in the up and down stream sections of the impounded zone of the river Ganga in the foothills. Tropical Ecol. 45 (2): 251-261, ISSN 0564-3295.

Boyero, L. (2002): Insect biodiversity in fresh water ecosystem: is there any latitudinal gradient? Marine and Fresh water research 53, 753-755.

Briers, R.A. and Biggs, J. (2005): Spatial patterns in Pond invertebrate communities: separating environmental and distance effects. Aquatic conservation. Marine and Fresh water ecosystem 15, 549-557.

Careghino, R., Park, V., Compin, A. and Lek, S. (2003): Predicting the species richness of aquatic insects in streams using a limited number of environmental variables. Journal of  North Americal Benthological Society 22, 442-456.

Chessman, B. C. (1986): dietary studies of aquatic insects from two Victorian rivers, Australian Journal of Marine fresh water Res. 37:129-146.

Clarke, A., MacNally, R., Bond, N. and Lake, P.S. (2008): Macroinvertibrate diversity in headwater streams: a review. Fresh water Biology 53, 1707-1721.

Dicks, L.V., Corbet, S.A., Pywell, R.F. (2003): Compartmentalization in plant-insect flower visitor web. J.Animal Ecol., 71,32-43.

Death, R.G. and Zimmermann, E.M. (2005): Interaction between disturbance and primary productivity in determining stream invertibrate diversity. Oikos 111, 392-402.

Dobson,M(1994): Micro habitat as a determinant of diversity:stream invertebrates colonizing leaf packs .Fresh water Biol.32;565-572.

Douglas,A.E. (1993); The nutritional quality of phloem sap utilized by natural aphid population,Eco. Entomol.,18, 31-38.

Erman, N.A. (1984): The use of riparian system by aquatic insects.pp.177-182.in R.E.Warner and Hendni, California riparian system, Davis C.A.

Gallego L.R.A., E. Meerhoff, J. M. Clemente and D. Conde (2010): Can ephemeral proliferations of submerged macrophytes influence zoobenthos and water quality in coastal lagoons? Hydrobiol. Springer Netherlands, Vol.646, 1573-5117 (online) Biomedical and Lifescience, pp.253-269.

Giulio,M.D. and Edwards,P.J. (2003): The influence of host plant diversity and food quality on larval survival of plant fedding heteropteran bugs.Swiss Federal Res. Sta. Agroeco and Agri., Geobotanical Ins. Zurish Switzerland,Eco.Ent.28,51-57.

Haslam, S.M. (1978): River plants,the macrophytic vegetation of water course, Cambridge University Press, London, pp 396.

Hector, A., Schmid, B., Beierkuhnlein, C., Caldeira, M.C., Diemer, M. Dimitrakopoulos, P.G. (1999): Plant diversity and productivity experiments in European grassland. Science, 286, 1123-1127.

Hilsenhoff, W.L. (1977): Use of Arthropods to evaluate water quality of stream, Tech. Bull.No.100 Deptt. Nat. Res. Madison, Wilcosin, pp. 1-15.

Hunter, M.D. (2001): Multiple approaches to estimating the relative importance of top-down and bottom-up forces on insects populatins,experiments, life tables and time series analysis. Basic and applied Eco. 2, 295-309.

Hynes, H. B. N. (1970): The ecology of running waters. Uni.of Toronto; Toronto Press, pp.555.

Knapp R. (1984): Conservations on quantitative parameters and qualitative attributes in vegetation analysis: Sampling method and taxon analysis. Vegetation Science, W.J. publication hague, 958pp

Lill, J.T., Marquis, R.J.and Ricklefs, R.E. (2002): Host plant influence parasitism of forest caterpiller. Nature, 417, 170-173.

 Merrit,R. W. and K. W. Cummins,(1978): An introduction to the aquatic insects of North America. Kendall Hunt. Dubuque, IOWA, pp. 441.

Needham J.G. and Needham P.R. (1962): A guide of the study of fresh water biology. Holdeom day Inc. San. Francisco, pp 108

Polis, G.A. and S.D. Hurd (1996): Linking marine and terrestrial food webs: allochthonous input from the ocean supports high secondary productivity on smoll islands and coastel land communities, An Nat. 143: 396-423.

Romanuk T.N. and C.D. Levings (2003): Association between Arthropods and the supralittoral Ecotone; dependence of aquatic and terrestrial taxo on riparian vegetation. Environ. Entomol. 32(6): 1343-1353.

William, J.O. (1998): Influence of temperature and humidity on the biology of insecticide-resistant and succeptible strains of Tribolium Castaneum (herbst.): Coleoptera Tenebrionidae. Insect Sci., Applic, vol.10, no.5, 607-625.

Yule, C. M. (1996): Trophic relationships and food webs of the benthic invertibrate fauna of two seasonal tropical streams on Bougainville Island, Papua New Guinea,Journal of Tropicl Ecology, 12:517-534.


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Monday, 22 April 2019

Ecological significance of MACROPHYTES

Dr. ASMA ALI (Ecologist)

INTRODUCTION :


Plants are described as aquatic, if the plant parts involved in photosynthesis are submerged or float on the water surface either permanently or at least for several months each year. The term macrophytes referred to all plants large enough to be visible to the necked eye, not only flowering plants but also ferns, brayophytes and algae.

Aquatic macrophytes are an important component of many water courses providing a structure and habitat for fish and invertebrates, offering protection against currents and predators, and forming a substrate for the deposition of eggs. As primary producer, macrophytes represent an important food resource and they also play a significant role in oxygen balance and nutrient cycle of many water courses. Macrophytes has a large ecological amplitude and therefore may colonize environments with different ecological characteristic.
            In view of their varying requirements, the composition of macrophyte species in a water body makes it possible to draw conclusions about a local chemical and physical conditions. Species that prefer low nutrients concentrations, in particular,  have become much less prevalent. Also in decline of species that are dependent on natural river banks withstanding and gravely substrate. Aquatic plants are especially sensitive to changes in nutrient concentrations and to organic pollutants.





[A]  Aquatic macrophytes as a link in the food chain
  1. Effect of fish grazing on nutrient release:-
  Herbivorous fish have a limited ability to convert plant material into animal tissue and to remove excess nutrients from the system. But being relatively efficient grazers and insufficient assimilators, they may play a significant part in initiating the internal, biologically mobilized nutrients source, or accelerate their recirculation. Thus, if with advancing eutrophication, the rate of macrophyte consumption increases due to the increase in number of herbivores, a new part of their biomass may finally be converted into additional algal biomass- the main troublemaker in lake of the temperate zone. Considerable information is available on the impact of grass carp grazing on water quality. Grass carp partially digest its food and the faeces are a large source of nutrients. Nutrients are readily utilised by phytoplankton, resulting in elevated algal Biomass, and in some situations leading to algal blooms.

2) Periphyton function:-
Periphyton is graze by a diversity of both invertebrate and vertebrate aquatic organisms. The invertebrates include molluscs, nematodes, microcrustaceans, amphipod and isopod crustaceans, crayfish, mysids, chironomid larvae, caddisfly and mayfly larvae. Invertebrate grazers may play an extremely important role in controlling Periphyton and showed cascading trophic interactions and also propose that fish predation on snails would enhance macrophyte biomass.

3) Zooplankton:-
Aquatic macrophytes provides shelter or refuge to zooplanktons, and the presence of especially large zooplanktons control small phytoplankton. If  the larger zooplanktons  becomes scare, the phytoplankton community will change to slow- growing bigger, mainly inedible blue-green species. These bigger, often colonial algae compete more successfully with the small algae for nutrients and establish high-density populations, sometimes leading to algal bloom. In turn ; this restrict light penetration into deeper water and leads to the death of submerged macrophytes.

4) Aquatic macroinvertebrates:-
Aquatic macrophytes are an important habitat for aquatic macroinvertebrates. The plants provide protection from predators and current, and are a direct and indirect source of food of fish and aquatic birds. In plant beds, benthic invertebrates are generally more numerous and more diverse than in open water. Indirectly, macrophytes are also important for the benthic macroinvertebrates, for which they provide protection against foraging by fish and aquatic birds, as well as providing the invertebrates with a supply of organic matter from the decomposing plants.

[B] The role of macrophytes in sustaining water level fluctuation:-
Shorelines are often defined by the relative influence of inflows of water, such as groundwater, precipitation and surface flow. The water level fluctuation of any water body is controlled by the water budget, as well as physical aspects of the surrounding environment such as soil permeability and most important the abundance of shoreline macrophytes, which directly modifies the physicochemical factors of the aquatic ecosystem such as soil makeup, redox potential and nutrient availability.

[C] The role of macrophytes in nutrient recycling among trophic levels and denitrification :-
Eutrophication of Lake water caused by excess nutrients level. Nonpoint source runoff from agricultural fields may contains high levels of nutrients, particularly nitrogen and phosphorus and can be a major contributor to eutrophication of water body. Water temperature and pH are driving factors in the rate of denitrification in an aquatic ecosystem and availability of carbon and nitrate work like a limiting factors. On the other hand various aquatic macrophytes also regulate nutrient level in aquous solutions.
Macrophytes are beneficial for nutrient mitigation since they are capable of some direct update in the water, increase hydraulic retention time by decreasing water flow, provide soil oxygenation and provides surface area for microbial biofilms. Macrophytes induced multiple beneficial effects for the conservation of the wetland, including sustaining water level, nutrients recycling among various trophic levels, provide shelter and growth to macro and micro invertebrates belonging to various orders.
         Aquatic macrophytes interacts with the physico-chemical environment as well as the biological community. These Complex interactions determine the community which is present in every wetland. It is important to have a good understanding of the interactions between plants and their environment.



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lmpact of pesticides on human health


      


Thresholds of pesticides:
Dr. Asma Ali (Ecologist)





Pest are unwanted small creatures that feeds on plants and harm them. To escape from damage, farmer utilize several specific methods for pest control. To reduce or inhibit the growth of pest, pesticides are often divided in the several different categories like insecticide, fungicides, rodenticides and herbicides.

    Pesticides are potentially toxic chemical and can have both acute and chronic health effects. Impact of pest depends on the quantity and the way in which a person is exposed. Several groups of pesticides  can remain in the soil and water for many years. 

The use of lethal pesticide have been banned in the developed countries but still most of the developing countries using them.  It has been observed that more than 1000 pesticides used around the world to ensure food would not destroyed by pest. 

As importantly most of the pesticides found to be soluble in water, therefore they applied with water, where they get absorbed by the target. The higher the solubility of the pesticides, the higher the risk of leaching.

Excessive rainfall and irrigation causes pesticides and its residues to be quickly transport to contaminate groundwater and freshwater supplies over large geographical area. Irrigating saturated soils or management is critical to minimise the risk of pesticides in infiltrating groundwater.



         The Cornell University Cooperative Extension states “cleanup of groundwater contaminated by pesticides is usually impossible. The slow movement of groundwater means that it may take decades for the contaminated water to flow beyond affected wells. Determining which wells will be affected and for how long is difficult problem.”

          When we deal with pesticide it meets a variety of fates. Some may be lost to the atmosphere through volatilization, carried away to surface water by runoff or broken down in the sunlight by photosynthesis.

Pesticides in soil maybe taken up by plants degraded into other chemical forms, or leached downward  possibly to groundwater. The remainder is retained  in the soil and continues to be available for plant uptake.

   Pesticides effects on human health by many ways. Organophosphates and Carbamates affected the nervous system while some of them irritate the skin or eyes. Some pesticide maybe carcinogens and others may affect the hormone or endocrine system in the body.



Although pesticides use has become very common worldwide, many new pest control methods are being developed. These alternative pest control methods are designed to help, control the pest population while protecting the environment and human health.


 The most common alternative pest control methods includes biological control, natural chemical control and genetic control.

In addition to these specific control method, a complex management system known as integrated pest management has also been developed. In addition, crops can be genetically altered in ways that produce chemical are physical barriers to prevent harm from pests.     

  I am at lost to understand that why are we using these banned toxic chemicals. Excess use of pesticides is going to be a helluva problem. We have many different methods to eliminate the damage of crop from these unwanted organism but we always want to take shortcut or adopt easy ways.

As mentioned by Reena Gupta (2017 November) in October 2017 about 40 farmers died and more than 700 were hospitalized in Maharashtra due to pesticide poisoning. Initial reports suggests that the death are due to monocrotophos; a highly toxic chemical been banned in more than 60 countries but allowed to be sold in our country. In this way all our past experiences are potentially available to the present. But what is pertinent here is to use alternative pest control method for sustainable development.


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Friday, 19 April 2019

Migratory birds : Unique guest of Bhopal

UPPER LAKE OF BHOPAL : The favourite destination of migratory birds.
Dr. ASMA ALI ( Ecologist)

As the sun was setting over the shore line of Upper Lake Bhopal, dozen of migratory birds were shuffling about lazily on the edge of the lake, the wind was fluffing  their feathers. A breeze picked up at the Shore line wrinkling the water as the Waves slowly rolled towards them.

Submerging the mud flats, where the birds had been feeding sticking their bills into the soft earth to dig up worms and crabs. Resting for hours on end, they can seem rather sedentary.

These birds had made an epic journey to get here flying all the way from their native place. Astonishingly, they didn't stop along the way. For 6 or 7 days straight they flew, beating their wings the entire way , about 5000-7000 miles. birds highly mobile creatures subject to their movements influenced daily, seasonally and annually, by weather, food and other factors which resulted in more or fewer species as well as individuals at any time in somewhat unpredictable ways.

               The first naturalist to write about migration was Aristotle, who observed that all migratory birds fatten themselves up before migration. Birds often double their weight in a day at a site, gaining up to 50% body fat to prepare them for the long leg of their journey. It is interesting to know that most birds migrate at an altitude of 3,000 feet or less but cranes and geese migrate at altitude of 15,000-21,000 feet.

             Bhopal with beautiful lakes have unique guest in peak of winter season. Many species of migratory birds such as Siberian crane, Greater Flamingo and Demoiselle crane arrive here from Europe, Central Asia and Himalayas, especially in winter season. Bhopal also known as the city of lakes have many natural and man made Lake offer a perfect habitat for these visitors.

             Between 1500 and 4000 species of birds are known to migrate in India and South Asia. In India subcontinent the majority of migratory birds are winter migraine Birds plays important role in ecosystem which are good pollinator and Predator of insects and small mammals, birds also helps dispersing of seed. But immigration of birds on Upper lake has drastically reduce.

          The timing of migration seems to be controlled primarily by changes in day length. Migrating birds navigate using celestial clues from the Sun and stars, the Earth's magnetic field and mental map. Approximately 1800 of the world 10000 Bird species are long-distance migrants.

            Birds are among the few groups of organism in which both community reassembly and adaptation of species to climate change have been documented. Climate changes has resulted in birds shifting their ranges and colonizing new localities consequently, climate change has altered the species richness and composition of avian communities.

          We are learning more about the Migration of birds as they fly thousands of miles and how humans and climate change are making it tougher for them.



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