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Future of mobility analysis, with a focus on automotive cybersecurity VC investments and growth drivers

We introduce a model of traveling agents ({\it e.g.} frugivorous animals) who feed on randomly located vegetation patches and disperse their seeds, thus modifying the spatial distribution of resources in the long term. It is assumed that the survival probability of a seed increases with the distance to the parent patch and decreases with the size of the colonized patch. In turn, the foraging agents use a deterministic strategy with memory, that makes them visit the largest possible patches accessible within minimal travelling distances. The combination of these interactions produce complex spatio-temporal patterns. If the patches have a small initial size, the vegetation total mass (biomass) increases with time and reaches a maximum corresponding to a self-organized critical state with power-law distributed patch sizes and L\'evy-like movement patterns for the foragers. However, this state collapses as the biomass sharply decreases to reach a noisy stationary regime characterized by corrections to scaling. In systems with low plant competition, the efficiency of the foraging rules leads to the formation of heterogeneous vegetation patterns with $1/f^{\alpha}$ frequency spectra, and contributes, rather counter-intuitively, to lower the biomass levels.

We introduce a model of traveling agents ({\it e.g.} frugivorous animals) who feed on randomly located vegetation patches and disperse their seeds, thus modifying the spatial distribution of resources in the long term. It is assumed that the survival probability of a seed increases with the distance to the parent patch and decreases with the size of the colonized patch. In turn, the foraging agents use a deterministic strategy with memory, that makes them visit the largest possible patches accessible within minimal travelling distances. The combination of these interactions produce complex spatio-temporal patterns. If the patches have a small initial size, the vegetation total mass (biomass) increases with time and reaches a maximum corresponding to a self-organized critical state with power-law distributed patch sizes and L\'evy-like movement patterns for the foragers. However, this state collapses as the biomass sharply decreases to reach a noisy stationary regime characterized by corrections to scaling. In systems with low plant competition, the efficiency of the foraging rules leads to the formation of heterogeneous vegetation patterns with $1/f^{\alpha}$ frequency spectra, and contributes, rather counter-intuitively, to lower the biomass levels.

We introduce a model of traveling agents ({\it e.g.} frugivorous animals) who feed on randomly located vegetation patches and disperse their seeds, thus modifying the spatial distribution of resources in the long term. It is assumed that the survival probability of a seed increases with the distance to the parent patch and decreases with the size of the colonized patch. In turn, the foraging agents use a deterministic strategy with memory, that makes them visit the largest possible patches accessible within minimal travelling distances. The combination of these interactions produce complex spatio-temporal patterns. If the patches have a small initial size, the vegetation total mass (biomass) increases with time and reaches a maximum corresponding to a self-organized critical state with power-law distributed patch sizes and L\'evy-like movement patterns for the foragers. However, this state collapses as the biomass sharply decreases to reach a noisy stationary regime characterized by corrections to scaling. In systems with low plant competition, the efficiency of the foraging rules leads to the formation of heterogeneous vegetation patterns with $1/f^{\alpha}$ frequency spectra, and contributes, rather counter-intuitively, to lower the biomass levels.

We introduce a model of traveling agents ({\it e.g.} frugivorous animals) who feed on randomly located vegetation patches and disperse their seeds, thus modifying the spatial distribution of resources in the long term. It is assumed that the survival probability of a seed increases with the distance to the parent patch and decreases with the size of the colonized patch. In turn, the foraging agents use a deterministic strategy with memory, that makes them visit the largest possible patches accessible within minimal travelling distances. The combination of these interactions produce complex spatio-temporal patterns. If the patches have a small initial size, the vegetation total mass (biomass) increases with time and reaches a maximum corresponding to a self-organized critical state with power-law distributed patch sizes and L\'evy-like movement patterns for the foragers. However, this state collapses as the biomass sharply decreases to reach a noisy stationary regime characterized by corrections to scaling. In systems with low plant competition, the efficiency of the foraging rules leads to the formation of heterogeneous vegetation patterns with $1/f^{\alpha}$ frequency spectra, and contributes, rather counter-intuitively, to lower the biomass levels.

http://uf.catalog.fcla.edu/uf.jsp?st=UF028627459&ix=pm&I=0&V=D&pm=1

http://uf.catalog.fcla.edu/uf.jsp?st=UF028627459&ix=pm&I=0&V=D&pm=1

http://uf.catalog.fcla.edu/uf.jsp?st=UF028627459&ix=pm&I=0&V=D&pm=1

Includes bibliographical references (p. 207-217) and index

Includes bibliographical references (p. 207-217) and index

Includes bibliographical references (p. 207-217) and index

Foraging has become quite a hobby for some folks, but getting started can be intimidating. For many years I used to run workshops and courses in the UK, and the attached botanical notes were part of a day-long long-distance trek. I thought they might be useful for someone starting out.

Foraging has become quite a hobby for some folks, but getting started can be intimidating. For many years I used to run workshops and courses in the UK, and the attached botanical notes were part of a day-long long-distance trek. I thought they might be useful for someone starting out.

Foraging has become quite a hobby for some folks, but getting started can be intimidating. For many years I used to run workshops and courses in the UK, and the attached botanical notes were part of a day-long long-distance trek. I thought they might be useful for someone starting out.

xiv, 219 p., [8 p. of plates] : 30 cm

xiv, 219 p., [8 p. of plates] : 30 cm

xiv, 219 p., [8 p. of plates] : 30 cm

Honey bees are important pollinators, requiring floral pollen and nectar for nutrition. Nectar is rich in sugars, but contains additional nutrients, including amino acids (AAs). We tested the preferences of free-flying foragers between 20 AAs at 0.1% w/w in sucrose solutions in an artificial meadow. We found consistent preferences amongst AAs, with essential AAs preferred over nonessential AAs. The preference of foragers correlated negatively with AA induced deviations in pH values, as compared to the control. Next, we quantified tradeoffs between attractive and deterrent AAs at the expense of carbohydrates in nectar. Bees were attracted by phenylalanine, willing to give up 84 units sucrose for 1 unit AA. They were deterred by glycine, and adding 100 or more units of sucrose could resolve to offset 1 unit AA. In addition, we tested physiological effects of AA nutrition on forager homing performance. In a no-choice context, caged bees showed indifference to 0.1% proline, leucine, glycine or phenylanaline in sucrose solutions. Furthermore, flight tests gave no indication that AA nutrition affected flight capacity directly. In contrast, low carbohydrate nutrition reduced the performance of bees, with important methodological implications for homing studies that evaluate the effect of substances that may affect imbibition of sugar solution. In conclusion, low AA concentrations in nectar relative to pollen suggest a limited role in bee nutrition. Most of the 20 AAs evoked a neutral to a mild deterrent response in bees, thus it seems unlikely that bees respond to AAs in nectar as a cue to assess nutritional quality. Nonetheless, free choice behavior of foraging bees is influenced, for instance by phenylalanine and glycine. Thus, AAs in nectar may affect plant-pollinator interactions and thereby exhibit a selective pressure on the flora in the honey bee habitat.

Honey bees are important pollinators, requiring floral pollen and nectar for nutrition. Nectar is rich in sugars, but contains additional nutrients, including amino acids (AAs). We tested the preferences of free-flying foragers between 20 AAs at 0.1% w/w in sucrose solutions in an artificial meadow. We found consistent preferences amongst AAs, with essential AAs preferred over nonessential AAs. The preference of foragers correlated negatively with AA induced deviations in pH values, as compared to the control. Next, we quantified tradeoffs between attractive and deterrent AAs at the expense of carbohydrates in nectar. Bees were attracted by phenylalanine, willing to give up 84 units sucrose for 1 unit AA. They were deterred by glycine, and adding 100 or more units of sucrose could resolve to offset 1 unit AA. In addition, we tested physiological effects of AA nutrition on forager homing performance. In a no-choice context, caged bees showed indifference to 0.1% proline, leucine, glycine or phenylanaline in sucrose solutions. Furthermore, flight tests gave no indication that AA nutrition affected flight capacity directly. In contrast, low carbohydrate nutrition reduced the performance of bees, with important methodological implications for homing studies that evaluate the effect of substances that may affect imbibition of sugar solution. In conclusion, low AA concentrations in nectar relative to pollen suggest a limited role in bee nutrition. Most of the 20 AAs evoked a neutral to a mild deterrent response in bees, thus it seems unlikely that bees respond to AAs in nectar as a cue to assess nutritional quality. Nonetheless, free choice behavior of foraging bees is influenced, for instance by phenylalanine and glycine. Thus, AAs in nectar may affect plant-pollinator interactions and thereby exhibit a selective pressure on the flora in the honey bee habitat.

We explore a two-step optimization problem in random environments, the so-called restaurant-coffee shop problem, where a walker aims at visiting the nearest and better restaurant in an area and then move to the nearest and better coffee-shop. This is an extension of the Tourist Problem, a one-step optimization dynamics that can be viewed as a deterministic walk in a random medium. A certain amount of heterogeneity in the values of the resources to be visited causes the emergence of power-laws distributions for the steps performed by the walker, similarly to a L\'{e}vy flight. The fluctuations of the step lengths tend to decrease as a consequence of multiple-step planning, thus reducing the foraging uncertainty. We find that the first and second steps of each planned movement play very different roles in heterogeneous environments. The two-step process improves only slightly the foraging efficiency compared to the one-step optimization, at a much higher computational cost. We discuss the implications of these findings for animal and human mobility, in particular in relation to the computational effort that informed agents should deploy to solve search problems.

We explore a two-step optimization problem in random environments, the so-called restaurant-coffee shop problem, where a walker aims at visiting the nearest and better restaurant in an area and then move to the nearest and better coffee-shop. This is an extension of the Tourist Problem, a one-step optimization dynamics that can be viewed as a deterministic walk in a random medium. A certain amount of heterogeneity in the values of the resources to be visited causes the emergence of power-laws distributions for the steps performed by the walker, similarly to a L\'{e}vy flight. The fluctuations of the step lengths tend to decrease as a consequence of multiple-step planning, thus reducing the foraging uncertainty. We find that the first and second steps of each planned movement play very different roles in heterogeneous environments. The two-step process improves only slightly the foraging efficiency compared to the one-step optimization, at a much higher computational cost. We discuss the implications of these findings for animal and human mobility, in particular in relation to the computational effort that informed agents should deploy to solve search problems.

We explore a two-step optimization problem in random environments, the so-called restaurant-coffee shop problem, where a walker aims at visiting the nearest and better restaurant in an area and then move to the nearest and better coffee-shop. This is an extension of the Tourist Problem, a one-step optimization dynamics that can be viewed as a deterministic walk in a random medium. A certain amount of heterogeneity in the values of the resources to be visited causes the emergence of power-laws distributions for the steps performed by the walker, similarly to a L\'{e}vy flight. The fluctuations of the step lengths tend to decrease as a consequence of multiple-step planning, thus reducing the foraging uncertainty. We find that the first and second steps of each planned movement play very different roles in heterogeneous environments. The two-step process improves only slightly the foraging efficiency compared to the one-step optimization, at a much higher computational cost. We discuss the implications of these findings for animal and human mobility, in particular in relation to the computational effort that informed agents should deploy to solve search problems.

We explore a two-step optimization problem in random environments, the so-called restaurant-coffee shop problem, where a walker aims at visiting the nearest and better restaurant in an area and then move to the nearest and better coffee-shop. This is an extension of the Tourist Problem, a one-step optimization dynamics that can be viewed as a deterministic walk in a random medium. A certain amount of heterogeneity in the values of the resources to be visited causes the emergence of power-laws distributions for the steps performed by the walker, similarly to a L\'{e}vy flight. The fluctuations of the step lengths tend to decrease as a consequence of multiple-step planning, thus reducing the foraging uncertainty. We find that the first and second steps of each planned movement play very different roles in heterogeneous environments. The two-step process improves only slightly the foraging efficiency compared to the one-step optimization, at a much higher computational cost. We discuss the implications of these findings for animal and human mobility, in particular in relation to the computational effort that informed agents should deploy to solve search problems.

Gender segregation in early-childhood social play is a pervasive pattern in North America, and child-development scholars have suggested it is a human universal. But very few researchers have looked at gender segregation in small-scale societies, particularly those of hunter-gatherers, whom the authors here call foragers. The authors present their observations of fifty-six, one- to four-year-old children living in two small-scale cultures--Bofi farmers and Bofi foragers--in Central Africa. They examined gender and age variation in the social play of these two groups and found that three- to four-year-olds became more segregated by gender than one- to two-year-olds and that boys in particular showed a tendency to play with other boys. The authors also found that cultural differences became more manifest as gender segregation grew more prominent among the children of Bofi farmers than Bofi foragers. (Contains 1 figure.)

Gender segregation in early-childhood social play is a pervasive pattern in North America, and child-development scholars have suggested it is a human universal. But very few researchers have looked at gender segregation in small-scale societies, particularly those of hunter-gatherers, whom the authors here call foragers. The authors present their observations of fifty-six, one- to four-year-old children living in two small-scale cultures--Bofi farmers and Bofi foragers--in Central Africa. They examined gender and age variation in the social play of these two groups and found that three- to four-year-olds became more segregated by gender than one- to two-year-olds and that boys in particular showed a tendency to play with other boys. The authors also found that cultural differences became more manifest as gender segregation grew more prominent among the children of Bofi farmers than Bofi foragers. (Contains 1 figure.)

Gender segregation in early-childhood social play is a pervasive pattern in North America, and child-development scholars have suggested it is a human universal. But very few researchers have looked at gender segregation in small-scale societies, particularly those of hunter-gatherers, whom the authors here call foragers. The authors present their observations of fifty-six, one- to four-year-old children living in two small-scale cultures--Bofi farmers and Bofi foragers--in Central Africa. They examined gender and age variation in the social play of these two groups and found that three- to four-year-olds became more segregated by gender than one- to two-year-olds and that boys in particular showed a tendency to play with other boys. The authors also found that cultural differences became more manifest as gender segregation grew more prominent among the children of Bofi farmers than Bofi foragers. (Contains 1 figure.)

Gender segregation in early-childhood social play is a pervasive pattern in North America, and child-development scholars have suggested it is a human universal. But very few researchers have looked at gender segregation in small-scale societies, particularly those of hunter-gatherers, whom the authors here call foragers. The authors present their observations of fifty-six, one- to four-year-old children living in two small-scale cultures--Bofi farmers and Bofi foragers--in Central Africa. They examined gender and age variation in the social play of these two groups and found that three- to four-year-olds became more segregated by gender than one- to two-year-olds and that boys in particular showed a tendency to play with other boys. The authors also found that cultural differences became more manifest as gender segregation grew more prominent among the children of Bofi farmers than Bofi foragers. (Contains 1 figure.)

Gender segregation in early-childhood social play is a pervasive pattern in North America, and child-development scholars have suggested it is a human universal. But very few researchers have looked at gender segregation in small-scale societies, particularly those of hunter-gatherers, whom the authors here call foragers. The authors present their observations of fifty-six, one- to four-year-old children living in two small-scale cultures--Bofi farmers and Bofi foragers--in Central Africa. They examined gender and age variation in the social play of these two groups and found that three- to four-year-olds became more segregated by gender than one- to two-year-olds and that boys in particular showed a tendency to play with other boys. The authors also found that cultural differences became more manifest as gender segregation grew more prominent among the children of Bofi farmers than Bofi foragers. (Contains 1 figure.)

We present a differential equation-based mathematical model of nectar foraging by the honey bee Apis mellifera. The model focuses on two behavioural classes; nectar foragers and nectar receivers. Results generated from the model are used to demonstrate how different classes within a collective can collaborate to combine information and produce finely tuned decisions through simple interactions. In particular we show the importance of the `search time' - the time a returning forager takes to find an available nectar receiver - in restricting the forager population to a level consistent with colony-wide needs.

travel linearity and speed of human foragers and chimpanzees during their daily search for food in tropical rainforests Haneul Jang Christophe Boesch Roger Mundry Simone D. Ban Karline R. L. Janmaat

travel linearity and speed of human foragers and chimpanzees during their daily search for food in tropical rainforests Haneul Jang Christophe Boesch Roger Mundry Simone D. Ban Karline R. L. Janmaat

travel linearity and speed of human foragers and chimpanzees during their daily search for food in tropical rainforests Haneul Jang Christophe Boesch Roger Mundry Simone D. Ban Karline R. L. Janmaat

Includes index

Includes index

Includes index

Includes index

Includes index

Includes index

We study a simple model of a forager as a walk that modifies a relaxing substrate. Within it simplicity, this provides an insight on a number of relevant and non-intuitive facts. Even without memory of the good places to feed and no explicit cost of moving, we observe the emergence of a finite home range. We characterize the walks and the use of resources in several statistical ways, involving the behavior of the average used fraction of the system, the length of the cycles followed by the walkers, and the frequency of visits to plants. Preliminary results on population effects are explored by means of a system of two non directly interacting animals. Properties of the overlap of home ranges show the existence of a set of parameters that provides the best utilization of the shared resource.

We study a simple model of a forager as a walk that modifies a relaxing substrate. Within it simplicity, this provides an insight on a number of relevant and non-intuitive facts. Even without memory of the good places to feed and no explicit cost of moving, we observe the emergence of a finite home range. We characterize the walks and the use of resources in several statistical ways, involving the behavior of the average used fraction of the system, the length of the cycles followed by the walkers, and the frequency of visits to plants. Preliminary results on population effects are explored by means of a system of two non directly interacting animals. Properties of the overlap of home ranges show the existence of a set of parameters that provides the best utilization of the shared resource.

We study a simple model of a forager as a walk that modifies a relaxing substrate. Within it simplicity, this provides an insight on a number of relevant and non-intuitive facts. Even without memory of the good places to feed and no explicit cost of moving, we observe the emergence of a finite home range. We characterize the walks and the use of resources in several statistical ways, involving the behavior of the average used fraction of the system, the length of the cycles followed by the walkers, and the frequency of visits to plants. Preliminary results on population effects are explored by means of a system of two non directly interacting animals. Properties of the overlap of home ranges show the existence of a set of parameters that provides the best utilization of the shared resource.

We study a simple model of a forager as a walk that modifies a relaxing substrate. Within it simplicity, this provides an insight on a number of relevant and non-intuitive facts. Even without memory of the good places to feed and no explicit cost of moving, we observe the emergence of a finite home range. We characterize the walks and the use of resources in several statistical ways, involving the behavior of the average used fraction of the system, the length of the cycles followed by the walkers, and the frequency of visits to plants. Preliminary results on population effects are explored by means of a system of two non directly interacting animals. Properties of the overlap of home ranges show the existence of a set of parameters that provides the best utilization of the shared resource.

We study a simple model of a forager as a walk that modifies a relaxing substrate. Within it simplicity, this provides an insight on a number of relevant and non-intuitive facts. Even without memory of the good places to feed and no explicit cost of moving, we observe the emergence of a finite home range. We characterize the walks and the use of resources in several statistical ways, involving the behavior of the average used fraction of the system, the length of the cycles followed by the walkers, and the frequency of visits to plants. Preliminary results on population effects are explored by means of a system of two non directly interacting animals. Properties of the overlap of home ranges show the existence of a set of parameters that provides the best utilization of the shared resource.

We study a simple model of a forager as a walk that modifies a relaxing substrate. Within it simplicity, this provides an insight on a number of relevant and non-intuitive facts. Even without memory of the good places to feed and no explicit cost of moving, we observe the emergence of a finite home range. We characterize the walks and the use of resources in several statistical ways, involving the behavior of the average used fraction of the system, the length of the cycles followed by the walkers, and the frequency of visits to plants. Preliminary results on population effects are explored by means of a system of two non directly interacting animals. Properties of the overlap of home ranges show the existence of a set of parameters that provides the best utilization of the shared resource.

We study a simple model of a forager as a walk that modifies a relaxing substrate. Within it simplicity, this provides an insight on a number of relevant and non-intuitive facts. Even without memory of the good places to feed and no explicit cost of moving, we observe the emergence of a finite home range. We characterize the walks and the use of resources in several statistical ways, involving the behavior of the average used fraction of the system, the length of the cycles followed by the walkers, and the frequency of visits to plants. Preliminary results on population effects are explored by means of a system of two non directly interacting animals. Properties of the overlap of home ranges show the existence of a set of parameters that provides the best utilization of the shared resource.

A book discussing human values in relation to the environment

A book discussing human values in relation to the environment

A book discussing human values in relation to the environment

A book discussing human values in relation to the environment

A book discussing human values in relation to the environment