Avian Assemblages at Bird Baths: A Comparison of Urban and Rural Bird Baths in Australia

Private gardens provide habitat and resources for many birds living in human-dominated landscapes. While wild bird feeding is recognised as one of the most popular forms of human-wildlife interaction, almost nothing is known about the use of bird baths. This citizen science initiative explores avian assemblages at bird baths in private gardens in south-eastern Australia and how this differs with respect to levels of urbanisation and bioregion. Overall, 992 citizen scientists collected data over two, four-week survey periods during winter 2014 and summer 2015 (43% participated in both years). Avian assemblages at urban and rural bird baths differed between bioregions with aggressive nectar-eating species influenced the avian assemblages visiting urban bird baths in South Eastern Queensland, NSW North Coast and Sydney Basin while introduced birds contributed to differences in South Western Slopes, Southern Volcanic Plains and Victorian Midlands. Small honeyeaters and other small native birds occurred less often at urban bird baths compared to rural bird baths. Our results suggest that differences between urban versus rural areas, as well as bioregion, significantly influence the composition of avian assemblages visiting bird baths in private gardens. We also demonstrate that citizen science monitoring of fixed survey sites such as bird baths is a useful tool in understanding large-scale patterns in avian assemblages which requires a vast amount of data to be collected across broad areas.     

Swimming in mantids

The initiation, form of leg strokes and minimal requirements for swimming in Sphodromantis lineola are described.     

Springs in Swimming Animals

Animals can lower the metabolic cost of swimming by using appropriatelytuned, elastic springs. Jet-powered invertebrates use springsthat lie in functional parallel to their swimming muscles topower half the locomotor cycle. The parallel geometry constrainsthe spring to be non-linearly elastic; muscle power is divertedto load the spring only when swimming muscles are not capableof producing maximal hydrodynamic thrust. The springs of jellyfishand scallops are forced at or near their resonant frequency,producing large energy savings. Measuring the contribution ofelastic energy storage to jet-powered locomotion has been facilitatedby the relatively simple geometries of invertebrate locomotorsystems. In contrast, complex musculoskeletal systems and kinematicshave complicated the study of springs in swimming vertebrates.Skins, tendons and axial skeletons of some vertebrate swimmershave appropriate mechanical properties to act as springs. Todate, though, there exist just a handful of studies that haveinvestigated the mechanical behaviors of these locomotor structuresin swimming vertebrates, and these data have yet to be integratedwith measures of swimming power. Integrating mechanical, kinematic,hydrodynamic and metabolic data are required to understand morefully the role of elastic springs in vertebrate swimming energetics.     

Swimming Performance Assessment in Fishes

Swimming performance tests of fish have been integral to studies of muscle energetics, swimming mechanics, gas exchange, cardiac physiology, disease, pollution, hypoxia and temperature. This paper describes a flexible protocol to assess fish swimming performance using equipment in which water velocity can be controlled. The protocol involves one to several stepped increases in flow speed that are intended to cause fish to fatigue. Step speeds and their duration can be set to capture swimming abilities of different physiological and ecological relevance. Most frequently step size is set to determine critical swimming velocity (U_crit), which is intended to capture maximum sustained swimming ability. Traditionally this test has consisted of approximately ten steps each of 20 min duration. However, steps of shorter duration (e.g. 1 min) are increasingly being utilized to capture acceleration ability or burst swimming performance. Regardless of step size, swimming tests can be repeated over time to gauge individual variation and recovery ability. Endpoints related to swimming such as measures of metabolic rate, fin use, ventilation rate, and of behavior, such as the distance between schooling fish, are often included before, during and after swimming tests. Given the diversity of fish species, the number of unexplored research questions, and the importance of many species to global ecology and economic health, studies of fish swimming performance will remain popular and invaluable for the foreseeable future.     

Swimming mechanisms in nereidiform polychaetes

New observations of the swimming of several species of nereidiform polychaete are presented and the parameters of body motion analysed. It is shown that there are theoretical limits to the values of these parameters outside which propulsion by the wave motion of the body is impossible. Many of the observations do fall outside them. This is because of the effect of the beating parapodia. Kinematic considerations are introduced to show how the wave of parapodial activity is related to the wave motion of the body. Dynamic considerations lead to an estimate of the minimum Young's modulus of the parapodia for pure parapodial swimming, lower values being possible for a combination of body-wave and parapodial swimming. The speeds achieved by different methods of swimming are discussed for the species that have been examined.