scholarly journals Behavioural adaptations of argulid parasites (Crustacea: Branchiura) to major challenges in their life cycle

2015 ◽  
Vol 8 (1) ◽  
Author(s):  
V.N. Mikheev ◽  
A.F. Pasternak ◽  
E.T. Valtonen
2021 ◽  
pp. 31-33
Author(s):  
Priyanka Chandna

Waders belonging to order Charadriiformes are commonly found along shorelines and mudats that wade in order to forage for food (such as insects or crustaceans) in the mud or sand. Bogs, marshes, mudats, shorelines, ponds, and ooded areas are all popular habitats for wading birds. The waders include storks, spoonbills, cranes, herons, egrets and ibises. They have certain physical and behavioural adaptations for living on or near water. Wading birds depend on water as a source of food, shelter, and nesting sites. Wading birds wade into shallow water to obtain food, instead of swimming and diving in water in search of feed that is not found on land. If we study the morphology of wading birds, they have lots of characteristics and adaptations that are useful in a watery habitat. Long legs of the wading birds help them to keep their feathers high and dry when wading into water in search of food. A long neck and a long bill are adaptations that make it possible to strike at prey while walking around on long legs. The benets of wading bird′s long, thin, spread-out toes are three-fold: toes help them to keep their balance and also help them to walk in mud without sinking. While walking in water and mushy mud, thin toes are easier to lift and set down. Spread-out toes also prevent them from sinking into soft mud in the water and at the water's edge, and above all those toes also disperse the weight of these big, tall birds, helping them keep their balance over their long legs. Waders are ecologically dependent on wetlands, as they provide good habitat to them for feeding, roosting, breeding, nesting, pre-migratory requirements, migration and protection from predators. So, wet lands plays an important part in the life cycle of wading birds. Wetlands have got highest capacity and are often extremely rich in bird and animal life. The present study aims at the assessment of diversity and residential status of wading birds in Yamuna basin near Hodal in Palwal District. It is located at 27°53′39″N and 77°22′09″E having an average elevation of 190 meters. Many ornithologists pay lots of their attention on eld study of birds during the eighteenth, nineteenth and twentieth century and till today many more are involved in the study of avian diversity near rivers. Avian fauna of Kalesar forests in immediate vicinity of River Yamuna in Yamuna-nagar District has been analysed by Kalsi (1998). Kulkarni et al.(2011) reported 151 species of birds from river Godavari; Balapureet al. (2012) reported 63 avian species from river Narmada. Other workers like Bahuguna(2008), Taketal.(2010), Gupta & Kaushik (2011), Gupta et.al(2012), Anupma et al (2014), Ankita et al (2019) have studied wetlands birds in various regions along the banks of rivers.


Behaviour ◽  
2019 ◽  
Vol 156 (10) ◽  
pp. 969-996 ◽  
Author(s):  
Thomas Hesselberg ◽  
Daniel Simonsen ◽  
Carlos Juan

Abstract Interest for subterranean biology has risen sharply in recent years due to the simplicity of the cave environment. However, most studies have focussed on morphology with few studies looking at behaviour. The cave orb spiders show some unique behavioural adaptations compared to other orb spiders, including rudimentary orb webs, off-web foraging and a complex life cycle with a surface phase. Here, we compare these behavioural adaptations in the European Meta menardi and Meta bourneti to similar behaviours in surface-dwelling orb spiders. We find that current data suggest (1) an extreme reduction in the number of frame threads, (2) evidence of capturing non-flying prey, but not necessarily evidence for off-web foraging and (3) dispersal through a surface-dwelling life stage, but with data lacking on the role of ballooning and their return to caves. We conclude that Meta spiders have potential as model organisms for studies on behavioural adaptations and flexibility.


Author(s):  
Betty Ruth Jones ◽  
Steve Chi-Tang Pan

INTRODUCTION: Schistosomiasis has been described as “one of the most devastating diseases of mankind, second only to malaria in its deleterious effects on the social and economic development of populations in many warm areas of the world.” The disease is worldwide and is probably spreading faster and becoming more intense than the overall research efforts designed to provide the basis for countering it. Moreover, there are indications that the development of water resources and the demands for increasing cultivation and food in developing countries may prevent adequate control of the disease and thus the number of infections are increasing.Our knowledge of the basic biology of the parasites causing the disease is far from adequate. Such knowledge is essential if we are to develop a rational approach to the effective control of human schistosomiasis. The miracidium is the first infective stage in the complex life cycle of schistosomes. The future of the entire life cycle depends on the capacity and ability of this organism to locate and enter a suitable snail host for further development, Little is known about the nervous system of the miracidium of Schistosoma mansoni and of other trematodes. Studies indicate that miracidia contain a well developed and complex nervous system that may aid the larvae in locating and entering a susceptible snail host (Wilson, 1970; Brooker, 1972; Chernin, 1974; Pan, 1980; Mehlhorn, 1988; and Jones, 1987-1988).


Author(s):  
Randolph W. Taylor ◽  
Henrie Treadwell

The plasma membrane of the Slime Mold, Physarum polycephalum, process unique morphological distinctions at different stages of the life cycle. Investigations of the plasma membrane of P. polycephalum, particularly, the arrangements of the intramembranous particles has provided useful information concerning possible changes occurring in higher organisms. In this report Freeze-fracture-etched techniques were used to investigate 3 hours post-fusion of the macroplasmodia stage of the P. polycephalum plasma membrane.Microplasmodia of Physarum polycephalum (M3C), axenically maintained, were collected in mid-expotential growth phase by centrifugation. Aliquots of microplasmodia were spread in 3 cm circles with a wide mouth pipette onto sterile filter paper which was supported on a wire screen contained in a petri dish. The cells were starved for 2 hrs at 24°C. After starvation, the cells were feed semidefined medium supplemented with hemin and incubated at 24°C. Three hours after incubation, samples were collected randomly from the petri plates, placed in plancettes and frozen with a propane-nitrogen jet freezer.


1994 ◽  
Vol 11 (1) ◽  
pp. 47-56
Author(s):  
Virginia C. Day ◽  
Zachary F. Lansdowne ◽  
Richard A Moynihan ◽  
John A. Vitkevich

1978 ◽  
Vol 23 (2) ◽  
pp. 85-86
Author(s):  
BERTRAM J. COHLER
Keyword(s):  

1978 ◽  
Vol 23 (9) ◽  
pp. 697-697
Author(s):  
ALVIN G. BURSTEIN

1991 ◽  
Vol 36 (4) ◽  
pp. 333-333
Author(s):  
Marilyn Shatz
Keyword(s):  

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