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Some actions are intrinsic motor units that can be concatenated as needed to solve a problem. In contrast, many actions are correlated with one another when engaging in particular types of behaviour, such as predation, mating or aggression. Moreover, how those actions are associated depend on intrinsic rules of organisation. Consequently, selecting markers to measure as if they are independent may be misleading. For example, scoring success in grasping a piece of food may fail to reveal that different combinations of limb movements may be capable of comparable rates of success. The lack of independence among actions and the potentially misleading conclusions that can be drawn from end-point measures point us to the second principle – understanding the intrinsic organisation of behaviour. Knowing something about the intrinsic organisation of a behavioural sequence can be critical in identifying markers that reflect that organisation.
Traditionally, to test whether the hypothesised organisation of behaviour generates the behavioural markers selected for measurement has required experiments or comparisons across species, sex and age. In the last couple of decades, important strides have been made in developing ways to create virtual animals, either on a computer screen or as freely moving robots, that can be programmed to produce the behaviour of interest. If the programmed rules are sufficient to produce the behaviour of real animals, then that adds independent evidence for the proposed organisation. Novel testing methods is one direction for the future. Another is to identify additional organisational principles. For example, some level of randomness seems essential for the production of effective functional behaviour. A challenge for the future is to understand how random processes are integrated with the causal processes described in the preceding chapters.
Knowing the perceptions that an animal controls and the brain-based rules that regulate which actions are performed may not be sufficient to explain the overt behaviour performed. The reason for this is that the animal’s particular body anatomy and the structure of the environment within which the actions are performed may constrain them to a particular form. To be certain that it is perceptions or intrinsic motor organisation that is responsible for the behaviour being expressed, the role of body anatomy and environmental context needs to be assessed. These are the third and fourth principles of behavioural organisation. Without taking these principles into account, the behavioural markers selected for measurement may be misleadingly attributed to neural causes and evolutionary processes.
As an empirical science, the study of animal behaviour involves measurement. When an animal engages in a series of actions, such as exploring or catching prey, the problem becomes that of identifying suitable components from that stream of action to use as markers suitable to score. The markers selected reflect the observer’s hypothesis of the organisation of the behaviour. Unfortunately, in most cases, researchers only provide heuristic descriptions of what they measure. To make the study of animal behaviour more scientific, the hypotheses underlying the decision of what to measure should be made explicit so as to allow them to be tested. Using hypothesis testing as a guiding framework, several principles that have been shown to be useful in identifying behavioural organisation are presented, providing a starting point in deciding what markers to select for measurement.
Some actions are intrinsic motor units that can be concatenated as needed to solve a problem. In contrast, many actions are correlated with one another when engaging in particular types of behaviour, such as predation, mating or aggression. Moreover, how those actions are associated depend on intrinsic rules of organisation. Consequently, selecting markers to measure as if they are independent may be misleading. For example, scoring success in grasping a piece of food may fail to reveal that different combinations of limb movements may be capable of comparable rates of success. The lack of independence among actions and the potentially misleading conclusions that can be drawn from end-point measures point us to the second principle – understanding the intrinsic organisation of behaviour. Knowing something about the intrinsic organisation of a behavioural sequence can be critical in identifying markers that reflect that organisation.
Knowing the perceptions that an animal controls and the brain-based rules that regulate which actions are performed may not be sufficient to explain the overt behaviour performed. The reason for this is that the animal’s particular body anatomy and the structure of the environment within which the actions are performed may constrain them to a particular form. To be certain that it is perceptions or intrinsic motor organisation that is responsible for the behaviour being expressed, the role of body anatomy and environmental context needs to be assessed. These are the third and fourth principles of behavioural organisation. Without taking these principles into account, the behavioural markers selected for measurement may be misleadingly attributed to neural causes and evolutionary processes.
As an empirical science, the study of animal behaviour involves measurement. When an animal engages in a series of actions, such as exploring or catching prey, the problem becomes that of identifying suitable components from that stream of action to use as markers suitable to score. The markers selected reflect the observer’s hypothesis of the organisation of the behaviour. Unfortunately, in most cases, researchers only provide heuristic descriptions of what they measure. To make the study of animal behaviour more scientific, the hypotheses underlying the decision of what to measure should be made explicit so as to allow them to be tested. Using hypothesis testing as a guiding framework, several principles that have been shown to be useful in identifying behavioural organisation are presented, providing a starting point in deciding what markers to select for measurement.
When engaging in some behaviour, some actions by an animal are more likely to resonate with us as observers than others and those impressions often form the basis for the behavioural markers that we choose for measurement. However, as much as possible, we should view the context from the animal’s perspective as it is what is important to them that guides their behaviour. Of what the animal may be able to sense, some sensations rank as perceptions that are relevant to the animal in that context. Moreover, in dynamic situations, it is often those perceptions that the animal seeks to stabilise. This means the behaviour controls those perceptions, so many actions can be explained as being compensatory. Without knowing what an action is compensating for, actions may be mistakenly abstracted as markers to measure. So, the first principle is to identify the perceptions that are relevant to the animal.
The Pacific sleeper shark Somniosus pacificus is one of the largest predators in deep Suruga Bay, Japan. A single individual of the sleeper shark (female, ~300 cm in total length) was observed with two baited camera systems deployed simultaneously on the deep seafloor in the bay. The first arrival was recorded 43 min after the deployment of camera #1 on 21 July 2016 at a depth of 609 m. The shark had several remarkable features, including the snout tangled in a broken fishing line, two torn anteriormost left-gill septums, and a parasitic copepod attached to each eye. The same individual appeared at camera #2, which was deployed at a depth of 603 m, ~37 min after it disappeared from camera #1 view. Finally, the same shark returned to camera #1 ~31 min after leaving camera #2. The distance between the two cameras was 436 m, and the average groundspeed and waterspeed of the shark were 0.21 and 0.25 m s−1, respectively, which were comparable with those of the Greenland shark Somniosus microcephalus (0.22–0.34 m s−1) exhibiting the slowest comparative swimming speed among fish species adjusted for size. The ambient water temperature of the Pacific sleeper shark was 5.3 °C, which is considerably higher than that of the Greenland shark (~2 °C). Such a low swimming speed might be explained by the ‘visual interactions hypothesis’, but it is not a consequence of the negative effects of cold water on their locomotor organs.
All students and researchers of behaviour – from those observing freely-behaving animals in the field to those conducting more controlled laboratory studies – face the problem of deciding what exactly to measure. Without a scientific framework on which to base them, however, such decisions are often unsystematic and inconsistent. Providing a clear and defined starting point for any behavioural study, this is the first book to make available a set of principles for how to study the organisation of behaviour and, in turn, for how to use those insights to select what to measure. The authors provide enough theory to allow the reader to understand the derivation of the principles, and draw on numerous examples to demonstrate clearly how the principles can be applied. By providing a systematic framework for selecting what behaviour to measure, the book lays the foundations for a more scientific approach for the study of behaviour.
Measuring Behaviour is the established go-to text for anyone interested in scientific methods for studying the behaviour of animals or humans. It is widely used by students, teachers and researchers in a variety of fields, including biology, psychology, the social sciences and medicine. This new fourth edition has been completely rewritten and reorganised to reflect major developments in how behavioural studies are conducted. It includes new sections on the replication crisis, covering Open Science initiatives such as preregistration, as well as fully up-to-date information on the use of remote sensors, big data and artificial intelligence in capturing and analysing behaviour. The sections on the analysis and interpretation of data have been rewritten to align with current practices, with advice on avoiding common pitfalls. Although fully revised and revamped, this new edition retains the simplicity, clarity and conciseness that have made Measuring Behaviour a classic since the first edition appeared more than 30 years ago.
Dendrobranchiata shrimp taxonomic composition and spatial and temporal distribution on the Amazon continental shelf (ACS) were investigated along a transect between the sources of the Amazon and Pará Rivers, encompassing an extension of ~250 km towards the continental slope. Plankton was collected with oblique trawls (200 μm mesh size), and nine taxa were found; 59.4% were larvae (mysis or decapodid stages) and 40.6% were juveniles or adults. Acetes was negatively related to chlorophyll-a and temperature, and Luciferidae were positively correlated with months. This study provides novel information on the density distribution of dendrobranchiate shrimps, thus helping to pave the way to characterize a large-scale, hugely relevant area that is poorly studied. As in other tropical coastal areas, there is here an increase in number of taxa with increased distance from the coast. Luciferidae, Solenoceridae and Penaeidae were the most frequent families whereas Sicyoniidae and Sergestidae had the lowest frequency of occurrence nearer the slope. Despite the low larval density of penaeid shrimps, their presence in all months and at all sampling sites along the ACS proves the importance of this area for shrimps with socioeconomic relevance, as well as its importance as a nursery and growth habitat for dendrobranchiate shrimps.
The present study reports polychaetes that bore into limestone rocks along the east coast of the Aegean Sea (eastern Mediterranean). Rock materials were collected at two depth intervals (0–5 and 5–10 m) at 15 stations in four localities of Ildırı Bay. A total of 276 specimens belonging to 12 species and four families (Eunicidae, Spionidae, Cirratulidae and Sabellidae) were recorded. Specimens belonging to Dodecaceria and Pseudopotamilla were identified at the genus level, because they differ from described species, were few in number or were in poor condition. Dipolydora giardia is a new species to the marine fauna of Turkey. The most dominant and frequent family in the area was Eunicidae, followed by Spionidae. Lysidice ninetta and L. margaritacea comprised 59% of the total number of individuals. The number of species and individuals, and the diversity index did not change with regard to depth or locality. Two species assemblages were found in the area, mainly formed by Dipolydora and Lysidice species. The Lessepsian species, Palola valida, which is a new record for the Aegean Sea, occurred abundantly at the study sites, posing a risk of damage to limestone rocks in the Mediterranean Sea. The morphological features of the species identified at the generic level and the burrow structure of these species are presented. The burrow shapes of Palola siciliensis and P. valida were described for the first time in the present study; they constructed complicated galleries, including more than four entrances.