MOVEMENT AND WAYFINDING IN THE KING SAUD UNIVERSITY BUILT ENVIRONMENT: A LOOK AT FRESHMAN ORIENTATION AND ENVIRONMENTAL INFORMATION

One potentially significant, yet hardly investigated, criterion for postoccupancy evaluation is the legibility of a setting—the degree to which a building or group of buildings facilitate the ability of users to find their way around. Legibility is one of the foundation concepts of environmental psychology, yet it has not often been considered enough as a guiding principle in design. The purpose of this paper is to analyse spatial orientation and wayfinding problems encountered by newcomers (freshman students) at the King Saud University (KSU) campus, Saudi Arabia, and to test/relate this to Lynch's elements of the image of cities. The analysis draws on previous research findings, theories, and more general observations, as well as observations made of wayfinding performance and map sketching by 30 high-school students likely to soon enroll at the university. Many specific problems with orientation and the architectural legibility of the buildings are identified and discussed. Emphasis is placed upon physical-setting variables that are likely to affect the ease with which spatial orientation and wayfinding are accomplished. These include the following facets of the KSU built environment: degree of differentiation; degree of visual access; and complexity of spatial layout.Legible buildings within which people can effectively maintain their orientation and find their way, according to this research, are in no way simplistic, dull, or boring; on the contrary, settings must possess distinctive landmarks and regions which, along with understandable path networks, allow users to know where they are and how to make their way to desired destinations. Coherent and legible environments are important in the lives of the people who use them. The movement of people through buildings and the factors that influence whether or not they are able to find their way need to continue to be of significance to both researchers and practitioners.     

Modelling effects of time-variable exposure to the pyrethroid beta-cyfluthrin on rainbow trout early life stages

Background

Available literature and regulatory studies show that the severity of effects of beta-cyfluthrin (a synthetic pyrethroid) on fish is influenced by the magnitude and duration of exposure. To investigate how the exposure pattern to beta-cyfluthrin (constant vs peak) may influence the response of the fish, we used a mechanistic effect model to predict the survival and growth of the rainbow trout over its early life stages (i.e. egg, alevin and swim-up fry). We parameterized a toxicokinetic–toxicodynamic (TKTD) module in combination with a dynamic energy budget model enabling us to describe uptake and elimination, as well as to predict the threshold concentration for survival and sublethal effects (feeding behaviour and growth). This effect model was calibrated using data from an early life stage experiment where trout was exposed to a constant concentration of cyfluthrin. The model was validated by comparing model predictions to independent data from a pulsed-exposure study with early life stages of rainbow trout.

Results

The co-occurrence of effects on behaviour and growth raised the possibility that these were interrelated, i.e. impairment of feeding behaviour may have led to reduced food intake and slower growth. We, therefore, included ‘effect on feeding’ as mode of action in the TKTD module. At higher concentrations, the constant exposure led to death. The model was able to adequately capture this effect pattern in the calibration. The model was able to adequately predict the response of fish eggs, alevins and swim-up fry, from both the qualitative (response pattern) and quantitative points of view.

Conclusions

Since the model was successfully validated, it can be used to predict survival and growth of early life stages under various realistic time-variable exposure profiles (e.g. profiles from FOCUS surface water modelling) of beta-cyfluthrin.