Eric Posner’s signaling theory of social norms holds that individuals adopt social norms in order to signal that they have a low discount rate , and are therefore reliable long-term cooperative partners. This paper radically expands Posner’s theory by incorporating internalization into his model . I do this by tethering Posner’s theory to an evolutionary model. I argue that internalization is an adaptive quality that enhances the individual’s ability to play Posner’s signaling game and was (...) thus selected for. The idea that internalization is evolutionarily conditioned is not new; however, linking this to Posner’s theory of discount rate signals is, and doing so offers tremendous explanatory potential.Part I identifies the limitations of Posner’s purely rational choice approach, argues for the necessity of including internalization, and then proposes a model that does so – what I call the Expanded Signaling Model of Norms . Part II examines the problems that arise when we embrace such a model. How this model answers some key criticisms plaguing sociobiology is also briefly explored. Part III then examines existing criticisms of Posner’s theory, demonstrating how the Expanded Signaling Model clearly resolves these issues. The paper concludes that incorporating internalization into Posner’s signaling model greatly broadens the explanatory reach of Posner’s theory, providing a measure of clarity and predictability regarding how and why norms are internalized – an important insight, as these beliefs form the normative underpinning to law. (shrink)

Skyrms, building on the work of Dretske, has recently developed a novel information-theoretic account of propositional content in simple signalling systems. Information-theoretic accounts of content traditionally struggle to accommodate the possibility of misrepresentation, and I show that Skyrms’s account is no exception. I proceed to argue, however, that a modified version of Skyrms’s account can overcome this problem. On my proposed account, the propositional content of a signal is determined not by the information that it actually carries, but by the (...) information that it would carry at the nearest separating equilibrium of the underlying evolutionary dynamics. I show that this amended account yields reasonable ascriptions of false propositional content in a well-known formal model of the evolution of communication , and close with a discussion of the serious but perhaps not insuperable difficulties we face in applying the account to examples of signalling in the real world. (shrink)

Ethological theories usually attribute semantic content to animal signals. To account for this fact, many biologists and philosophers appeal to some version of teleosemantics. However, this picture has recently came under attack: while mainstream teleosemantics assumes that representational systems must cooperate, some biologists and philosophers argue that in certain cases signaling can evolve within systems lacking common interest. In this paper I defend the standard view from this objection.

GianCarlo Ghirardi passed away on June 1st, 201. He would have turned 83 on October 28, 2018. He was without any doubt one of the most prominent theoretical physicists working on the foundation and the philosophy of quantum mechanics. In this paper I review some of his achievements and underline how his research influenced the philosophy of physics community.

Living organisms are exposed to numerous influencing factors. This holds also true for their infrastructures that are processing and transducing information like endocrine networks or nerval channels. Therefore, the ability to compensate for noise is crucial for survival. An efficient mechanism to neutralise disturbances is instantiated in form of parallel complementary communication channels exerting antagonistic effects at their common receivers. Different signal processing types share the ability to suppress noise, to widen the system’s regulation capacity, and to provide for variable (...) gains while leaving the transferred signal to a large extent unchanged. (shrink)

This essay ties together some main strands of the author’s research spanning the last quarter-century. Because of its broad scope and space limitations, he prescinds from detailed arguments and instead intuitively motivates the general points which are supported more fully in other publications to which he provides references. After an initial delineation of several distinct notions of meaning, the author considers such a notion deriving from the evolutionary biology of communication that he terms ‘organic meaning’, and places it in the (...) context of evolutionary game theory. That provides a framework for a special type of organic meaning found in the phenomenon of expression, of which the author here offers an updated characterization while highlighting its wide philosophical interest. Expression in turn generalizes to a paradigmatic form of human communication—conversation—and section 4 provides a taxonomy of conversation-types while arguing that attention to such types helps to sharpen predictions of what speakers say rather than conversationally implicate. We close with a view of fictional discourse on which authors of fictional works are engaged in conversation with their readers, and can provide them with knowledge in spite of the fictional character of their conversation. Such knowledge includes knowledge of how an emotion feels and is thus a route to empathy. (shrink)

What is the content of a mental state? This question poses the problem of intentionality: to explain how mental states can be about other things, where being about them is understood as representing them. A framework that integrates predictive coding and signaling systems theories of cognitive processing offers a new perspective on intentionality. On this view, at least some mental states are evaluations, which differ in function, operation, and normativity from representations. A complete naturalistic theory of intentionality must (...) account for both types of intentional state. (shrink)

Vít Gvoždiak published a reconciliatory analysis of Searle’s social ontology with semiotics in Gvoždiak (2012). Without prior knowledge of his paper, an analysis of the same subject appeared in Msimang (2014). Even though Searle’s social ontology is a common point of reference in the formulation of semiotics in these papers, it also serves as a point of departure in their understanding of semiotics and its development. The semiotic theory expressed in Gvoždiak (2012) is an inherently linguistic (speech act centred) (...) theory, whereas the semiotic theory presented in Msimang (2014) tends more towards a general theory of communicative systems in which social ontology, which follows from speech act theory, is an interesting part. It is my purpose in this note to contrast the two positions of semiotic theory as they appear in the aforementioned papers in reference to their appropriation of Searle’s social ontology. (shrink)

Are strangers sincere in their moral praise and criticism? Here we apply signaling theory to argue ceteris paribus moral criticism is more likely sincere than praise; the former tends to be a higher-fidelity signal (in Western societies). To offer an example: emotions are often self-validating as a signal because they're hard to fake. This epistemic insight matters: moral praise and criticism influence moral reputations, and affect whether others will cooperate with us. Though much of this applies to generic (...) praise and criticism too, moral philosophers should value sincere moral praise and moral criticism for several reasons: it (i) offers insight into how others actually view us as moral agents; (ii) offers feedback to help us improve our moral characters; and (iii) encourages some behaviors, and discourages others. And so as moral agents, we should care whether moral praise and moral criticism is sincere. (shrink)

I offer two potential diagnoses of the behavioral norms governing post‐truth politics by comparing the view of language, communication, and truth‐telling put forward by David Lewis (extended by game theorists), and John Searle. My first goal is to specify the different ways in which Lewis, and game theorists more generally, in contrast to Searle (in the company of Paul Grice and Jurgen Habermas), go about explaining the normativity of truthfulness within a linguistic community. The main difference is that for Lewis (...) and game theorists, “truthful” signaling follows from an align- ment of interests, and deception follows from mixed motives leading to the calculation that sending false information is better for oneself. Following in the Enlightenment tradition, Searle argues that practical reasoning, which involves mastery of at least one language, requires that actors intend to communicate. This intention includes constraining the content of statements to uphold veracity conditions. After distinguishing between these two accounts, I will artic- ulate the implications for explaining, and even informing actions, constitutive of post‐truth politics. I argue that the strategic view of communication is suffi- cient neither to model everyday conversation nor to reflect a public sphere useful for democratic govern- ment. Both the pedagogy of strategic communication as cheap talk, and its concordance with new digital information technologies, challenge norms of truthful- ness that underlie modern institutions essential to an effective public sphere. (shrink)

How do conventions of communication emerge? How do sounds or gestures take on a semantic meaning, and how do pragmatic conventions emerge regarding the passing of adequate, reliable, and relevant information? My colleagues and I have attempted in earlier work to extend spatialized game theory to questions of semantics. Agent-based simulations indicate that simple signaling systems emerge fairly naturally on the basis of individual information maximization in environments of wandering food sources and predators. Simple signaling emerges by (...) means of any of various forms of updating on the behavior of immediate neighbors: imitation, localized genetic algorithms, and partial training in neural nets. Here the goal is to apply similar techniques to questions of pragmatics. The motivating idea is the same: the idea that important aspects of pragmatics, like important aspects of semantics, may fall out as a natural results of information maximization in informational networks. The attempt below is to simulate fundamental elements of the Gricean picture: in particular, to show within networks of very simple agents the emergence of behavior in accord with the Gricean maxims. What these simulations suggest is that important features of pragmatics, like important aspects of semantics, don't have to be added in a theory of informational networks. They come for free. (shrink)

Based on the wealth of scientific evidence and concepts, this theory has been formed, and its essence is as follows: 1. From the physical properties of the mind and those of the brain (the alive, processing brain), it can be concluded that the mind occurs, exists, and functions with the brain (Chapter 1) and that it is the composite of all neural information-processing processes (Chapter 2). 2. Qualia—mental phenomena that appear phenomenally in our mind and that we can consciously (...) experience, such as the vision of a house, the sound of a song, and the odor of a rose in our mind—are physical phenomena. They are governed by physical laws and are physically predictable. Specifically, they are neural-process–associated physical phenomena. (Chapters 3 & 4) 3. From the physical properties of qualia and those of special kinds of neural-process signaling patterns, which are neural information and non-material, it can be concluded that qualia are special kinds of neural-process signaling patterns, called special signaling patterns. (Chapter 5) 4. From the physical properties of consciousness and those of a special kind of reentrant signaling state, which is the neural information of the consciousness neural process and is non-material, it can be concluded that consciousness is a special kind of reentrant signaling state. 5. The fact that qualia and conscious awareness and conscious experiences of the qualia occur in only the final-stage sensory perception neural processes and the highest-level cognitive and executive neural processes, which are the latest-evolved neural processes, and never occur in the more primitive neural processes, such as the brainstem, cerebellum, and basal ganglia, or over the whole brain randomly, indicates that they are not haphazardly occurring phenomena but are evolved phenomena of the nervous system. (Chapter 5 & Chapter 6) 6. Because a neural process that performs a certain function (such as perceiving a vision) without a quale occurring and a neural process that performs that same function (such as perceiving the same vision) with a quale occurring have different information in the processes, they have different signaling patterns (to convey different information). Therefore, they have different physical effects on other neural processes, at least from the different effects of different signaling patterns. Qualia thus have physical effects. Also, because we do have conscious awareness and conscious experiences of qualia, qualia must certainly induce the consciousness neural process to function to be consciously aware of and to consciously experience the qualia. Therefore, because the consciousness neural process is a physical process, qualia cause changes in a physical process and thus have physical effects. (Chapter 5) Similarly, it can be concluded that consciousness (conscious awareness and conscious experiences) has physical effects. (Chapter 6) Therefore, qualia and consciousness are evolved neural functions that have physical effects. 7. Because a function requires resources in building, maintaining, and operating the function and may have some negative effects, if its overall effects do not help increase the survival chances of the animals that have the function, those animals and the function will likely become extinct in the evolutionary process. This is especially true for a major function in a critical organ, such as in the case of qualia and consciousness in the brain. The fact that qualia and consciousness still exist today indicates that they have been selected to remain in the evolutionary process. This means that their overall effects must help increase the survival chances of the species that have them. Qualia and consciousness, in the form that they are—phenomenal qualia and phenomenal consciousness, or qualia and consciousness that appear phenomenally in our mind—are thus evolved functions to help increase the survival chances of the species, including humans, that have them. This is the scientific answer to the other part of the hard problem of consciousness: Why do qualia and consciousness in the form of phenomenal qualia and phenomenal consciousness occur in this universe? This is also the scientific answer to one of the most basic questions of our lives: Why do “we” exist? (Chapter 5 & Chapter 6). (shrink)

When moral philosophers study ignorance, their efforts are almost exclusively confined to its exculpatory and blameworthy aspects. Unfortunately, though, this trend overlooks that certain kinds of propositional ignorance, namely of the personal costs and benefits of altruistic actions, can indirectly incentivize those actions. Humans require cooperation from others to survive, and that can be facilitated by a good reputation. One avenue to a good reputation is helping others, sticking to moral principles, and so forth, without calculating the personal costs of (...) doing so, e.g., saving someone from a burning building without calculating how personally costly or beneficial it would be. These actions are indirect moral benefits (partly) resulting from that kind of propositional ignorance. (shrink)

The lie detector test has long been treated with suspicion by the law. Recently, several authors have called this suspicion into question. They argue that the lie detector test may have considerable forensic benefits, particularly if we move past the classic, false-positive prone, autonomic nervous system-based (ANS-based) control question test, to the more reliable, brain-based, concealed information test. These authors typically rely on a “comparative advantage” argument to make their case. According to this argument, we should not be so suspicious (...) of lie detection evidence if it has comparative advantages over the epistemic methods currently utilised by the legal system. In this article, I add to this growing support by making a novel comparative advantage argument in favour of brain-based lie detection evidence. The argument focuses on the P300 concealed information test (P300 CIT), which has several unique properties, and on the effect it may have on pre-trial bargaining in criminal cases rather than in-court evidence. The thesis is that P300 CIT could allow for innocent defendants to credibly signal their innocence to investigators and prosecutors during pre-trial bargaining more effectively than current proposed methods for doing the same thing. I defend this argument from a number of objections, and suggest that it opens up an interesting avenue in the ongoing debate about the merits of this technology. Although the argument is presented with the criminal law in mind, it could form part of a more general cumulative case in favour of this technology. (shrink)

Declarations like “this meeting is adjourned” make certain facts the case by representing them as being the case. Yet surprisingly little attention has been paid to the mechanism whereby the utterance of a declaration can bring about a new state of affairs. In this paper, we use the incentivization account of institutional facts to address this issue. We argue that declarations can serve to bring about new states of affairs as their utterance have game theoretical import, typically in virtue of (...) the utterer signaling a commitment to act in an incentive-changing way. (shrink)

An important objection to signaling approaches to representation is that, if signaling behavior is driven by the maximization of usefulness, then signals will typically carry much more information about agent-dependent usefulness than about objective features of the world. This sort of considerations are sometimes taken to provide support for an anti-realist stance on representation itself. The author examines the game-theoretic version of this skeptical line of argument developed by Donald Hoffman and his colleagues. It is shown that their (...) argument only works under an extremely impoverished picture of the informational connections that hold between agent and world. In particular, it only works for cue-driven agents, in Kim Sterelny’s sense. In cases in which the agents’ understanding of what is useful results from combining pieces of information that reach them in different ways, and that complement one another, maximizing usefulness involves construing first a picture of agent-independent, objective matters of fact. (shrink)

There has recently been an explosion of formal models of signalling, which have been developed to learn about different aspects of meaning. This paper discusses whether that success can also be used to provide an original naturalistic theory of meaning in terms of information or some related notion. In particular, it argues that, although these models can teach us a lot about different aspects of content, at the moment they fail to support the idea that meaning just is some (...) kind of information. As an alternative, I suggest a more modest approach to the relationship between informational notions used in models and semantic properties in the natural world. (shrink)

One of the most important contributions in Roland Posner’s work (1993) was the extension and development of the Gricean paradigm on meaning (1957) in a systematic framework, providing thus a general foundation of semiotic phenomena. According to this approach, communication consists in behaviors or artifacts based on reciprocal assumptions about the intentions and beliefs of the subjects involved in a semiotic exchange. Posner’s model develops with clarity the hierarchical relationships of semiotic phenomena of different complexity, from simple pre-communicative behaviors (like (...) indicating or signaling) to full communicative acts. Not only limited to linguistic communication, this framework can be successfully extended in the description of all kind of sign production, from gestures to artifacts. This article discusses a key point of this paradigm, namely our faculty to at-tribute mental states to other individuals through the observation of their behavior, artifacts or texts. New insights from neuropsychology and developmental psychology are discussed in supporting the validity of this model of communication. (shrink)

There is a common assumption that evolutionary explanations of religion undermine religious beliefs. Do etiological accounts similarly affect the rationality of religious practices? To answer this question, this paper looks at two influential evolutionary accounts of ritual, the hazard-precaution model and costly signaling theory. It examines whether Cuneo’s account of ritual knowledge as knowing to engage God can be maintained in the light of these evolutionary accounts. While the evolutionary accounts under consideration are not metaphysically incompatible with the (...) idea that religious rituals engage God, they cast doubt on whether many, if not all, rituals can do this successfully. (shrink)

Grice, Lewis, and Skyrms proposed similar distinctions between kinds of meaning. The meaning of terms in human language, as Lewis and Skyrms had it, is ‘conventional’. Skyrms presented models showing how it is possible for conventional meaning to evolve in a population without reliance on pre-existing meaning. But one might think of conventionality as coming in degrees, based on whether the evolutionary process begins with ‘natural saliences’. We propose a theory of natural salience and several extensions of Skyrms’s models (...) to capture this notion. These models reveal that natural saliences can hinder, as well as help, the evolution of language. (shrink)

Recent work by Brian Skyrms offers a very general way to think about how information flows and evolves in biological networks — from the way monkeys in a troop communicate, to the way cells in a body coordinate their actions. A central feature of his account is a way to formally measure the quantity of information contained in the signals in these networks. In this paper, we argue there is a tension between how Skyrms talks of signalling networks and his (...) formal measure of information. Although Skyrms refers to both how information flows through networks and that signals carry information, we show that his formal measure only captures the latter. We then suggest that to capture the notion of flow in signalling networks, we need to treat them as causal networks. This provides the formal tools to define a measure that does capture flow, and we do so by drawing on recent work defining causal specificity. Finally, we suggest that this new measure is crucial if we wish to explain how evolution creates information. For signals to play a role in explaining their own origins and stability, they can’t just carry information about acts: they must be difference-makers for acts. (shrink)

Embodied cognitive science has argued that cognition is embodied principally in virtue of grossmorphological and sensorimotor features. This thesis argues that cognition is also internally embodied in affective and fine-grained physiological features whose transformative roles remain mostly unnoticed in contemporary cognitive science. I call this ‘proper embodiment’. I approach this larger subject by examining various emotion theories in philosophy and psychology. These tend to emphasise one of the many gross components of emotional processes, such as ‘feeling’ or ‘judgement’ to the (...) detriment of the others, often leading to an artificial emotion-cognition distinction even within emotion science itself. Attempts to reconcile this by putting the gross components back together, such as JessePrinz’s “embodied appraisal theory”, are, I argue, destined to failure because the vernacular concept of emotion which is used as the explanandum is not a natural kind and is not amenable to scientific explication.I examine Antonio Damasio’s proposal that emotion is involved in paradigmatic ‘cognitive’ processing such as rational decision making and argue (1) that the research he discusses does not warrant the particular hypothesis he favours, and (2) that Damasio’s account, though in many ways a step in the right direction, nonetheless continues to endorse a framework which sees affect and cognition as separate (though now highly interacting) faculties. I further argue that the conflation of ‘affect’ and 'emotion' may be the source of some confusion in emotion theory and that affect needs to be properly distinguished from ‘emotion’. I examine some dissociations in the pain literature which give us further empirical evidence that, as with the emotions, affect is a distinct component along with more cognitive elements of pain. I then argue that affect is distinctive in being grounded in homeostatic regulative activity in the body proper. With the distinction between affect, emotion, and cognition in hand, and the associated grounding of affect in bodily activity, I then survey evidence that bodily affect is also involved in perception and in paradigmatic cognitive processes such as attention and executive function. I argue that this relation is not ‘merely’ casual. Instead, affect (grounded in fine-grained details of internal bodily activity) is partially constitutive of cognition, participating in cognitive processing and contributing to perceptual and cognitive phenomenology. Finally I review some work in evolutionary robotics which reaches a similar conclusion, suggesting that the particular fine details of embodiment, such as molecular signalling between both neural and somatic cells matters to cognition. I conclude that cognition is properly embodied’ in that it is partially constituted by the many fine-grained bodily processes involved in affect (as demonstrated in the thesis) and plausibly by a wide variety of other fine-grained bodily processes that likewise tend to escape the net of contemporary cognitive science. (shrink)

Naturalistic theories of representation seek to specify the conditions that must be met for an entity to represent another entity. Although these approaches have been relatively successful in certain areas, such as communication theory or genetics, many doubt that they can be employed to naturalize complex cognitive representations. In this essay I identify some of the difficulties for developing a teleosemantic theory of cognitive representations and provide a strategy for accommodating them: to look into models of signaling (...) in evolutionary game theory. I show how these models can be used to formulate teleosemantics and expand it in new directions. (shrink)

What explains the distinctive features of human behavior? In this book, Stewart-Williams aims to answer this ambitious question. This book is an engaging addition to the already long list of recent attempts to provide an evolutionary explanation of human uniqueness. It is organized into six chapters, plus two appendices. These chapters address several key topics in evolutionary theory, sex differences and sexual behavior, altruism, and cultural evolution, albeit with varying degrees of detail and depth. These topics include sexual selection, (...) kin selection, Hamilton’s rule, reciprocal altruism, costly signaling theory, group selection, gene-centered views of evolution, inclusive fitness, proximate and ultimate evolutionary explanations, inbreeding avoidance, the Westermarck effect, jealousy, sperm competition, mating and parenting effort, cumulative cultural evolution, imitation and learning biases, evolutionary mismatch theories, and more. (shrink)

We introduce the virtual special issue on content in signalling systems. The issue explores the uses and limits of ideas from evolutionary game theory and information theory for explaining the content of biological signals. We explain the basic idea of the Lewis-Skyrms sender-receiver framework, and we highlight three key themes of the issue: (i) the challenge of accounting for deception, misinformation and false content, (ii) the relevance of partial or total common interest to the evolution of meaningful signals, (...) and (iii) how the sender-receiver framework relates to teleosemantics. (shrink)

Reciprocal Ethics is a novel ethical framework rooted in praxeology, the study of purposeful action. It represents an entirely new paradigm in moral philosophy, placing interaction at the core of universal ethics. Traditional ethical theories often divorce thought from action. Reciprocal Ethics contends that they are two aspects of the same phenomenon in the human experience, removing the traditional boundary between theoretical and practical ethics. The system categorizes all social interaction as either “self-directed” or “other-directed”, and by introducing the concept (...) of "normative signaling" it also exerts legitimate prescriptive power. The theory is a self-consistent, purely descriptive approach to ethics, that suggests that one's actions serve as semiotic signs that signal one's ethical stance in social interaction. Hence actions do not only define individual moral profiles, but also the moral ecosystem within which one actually operates. The theory operates in real time, adapting to the complexity of reality by taking into account uncertainty, incomplete data and social asymmetries. Reconciling elements of consequentialism and deontological theories, Reciprocal Ethics delivers a streamlined, yet comprehensive ethical system for social interaction, offering tangible insights for navigating complex moral dilemmas. By synthesizing descriptive metaethics and normative moral philosophy into one comprehensive formal theory, a bold assertion arises: Reciprocal Ethics becomes the Formal Science of Ethics. (shrink)

This paper proposes a new theory of the nature of hypocritical blame and why it is objectionable, arguing that hypocritical blame is a form of dishonest signaling. Blaming provides very important benefits: through its ability to signal our commitments to norms and unwillingness to tolerate norm violations, it greatly contributes to valuable norm-following. Hypocritical blamers, however, are insufficiently committed to the norms or values they blame others for violating. As allowing their blame to pass unchecked threatens the (...) class='Hi'>signaling system, our strong interest in maintaining valuable norm-following by tracking who has what commitments justifies objecting to hypocritical blame. This theory has a number of strengths over competing accounts: it delivers intuitive verdicts about when blame is objectionable across a range of cases, it is a naturalistic explanation, it is consistent with a leading theory of the nature of blame, it explains why hypocritical pronouncements that don’t feature blame are similiarly objectionable, it does not rely on contentious analyses of the nature of ‘standing’, and it preserves the common intuition that hypocrites are in some way dishonest. (shrink)

We consider how an epistemic network might self-assemble from the ritualization of the individual decisions of simple heterogeneous agents. In such evolved social networks, inquirers may be significantly more successful than they could be investigating nature on their own. The evolved network may also dramatically lower the epistemic risk faced by even the most talented inquirers. We consider networks that self-assemble in the context of both perfect and imperfect communication and compare the behaviour of inquirers in each. This provides a (...) step in bringing together two new and developing research programs, the theory of self-assembling games and the theory of network epistemology. (shrink)

Advances in neuroscience implicate reentrant signaling as the predominant form of communication between brain areas. This principle was used in a series of masking experiments that defy explanation by feed-forward theories. The masking occurs when a brief display of target plus mask is continued with the mask alone. Two masking processes were found: an early process affected by physical factors such as adapting luminance and a later process affected by attentional factors such as set size. This later process is (...) called masking by object substitution, because it occurs whenever there is a mismatch between the reentrant visual representation and the ongoing lower level activity. Iterative reentrant processing was formalized in a computational model that provides an excellent fit to the data. The model provides a more comprehensive account of all forms of visual masking than do the long-held feed-forward views based on inhibitory contour interactions. (shrink)

This paper develops a Fragmentalist theory of Presentism and shows how it can help to develop a interpretation of quantum mechanics. There are several fragmental interpretations of physics. In the interpretation of this paper, each quantum system forms a fragment, and fragment f1 makes a measurement on fragment f2 if and only if f2 makes a corresponding measurement on f1. The main idea is then that each fragment has its own present (or ‘now’) until a mutual quantum measurement—at which (...) time they come (‘become’) to share the same ‘now’. The theory of time developed here will make use of both McTaggart’s A-series (in the form of future-present-past) and B-series (earlier-times to later-times). An example of an application is that a Bell pair of electrons does not take on definite spin values until measurement because the measuring system and the Bell pair do not share the same present (‘now’) until mutual quantum measurement, i.e. until they ‘become’ to share the same A-series. Before that point the ‘now’ of the opposing system is not in the reference system’s fragment. Relativistic no-signaling is preserved within each fragment, which will turn out to be sufficient for the general case. Several issues in the foundations of quantum mechanics are canvassed, including Schrodinger’s cat, the Born rule, modifications to Minkowski space that accommodate both the A-series and the B-series, and entropy. (shrink)

The recent literature on causality has seen the introduction of several distinctions within causality, which are thought to be important for understanding the widespread scientific practice of focusing causal explanations on a subset of the factors that are causally relevant for a phenomenon. Concepts used to draw such distinctions include, among others, stability, specificity, proportionality, or actual-difference making. In this contribution, I propose a new distinction that picks out an explanatorily salient class of causes in biological systems. Some select causes (...) in complex biological systems, I argue, have the property of enabling coherent causal control of these systems. Examples of such control variables include hormones and other signaling molecules, e.g., TOR (target of rapamycin), morphogens or the products of homeotic selector genes in embryonic pattern formation. I propose an analysis of this notion based on concepts borrowed from causal graph theory. (shrink)

This paper brings together two erstwhile distinct strands of philosophical inquiry: the extended mind hypothesis and the situationist challenge to virtue theory. According to proponents of the extended mind hypothesis, the vehicles of at least some mental states (beliefs, desires, emotions) are not located solely within the confines of the nervous system (central or peripheral) or even the skin of the agent whose states they are. When external props, tools, and other systems are suitably integrated into the functional apparatus (...) of the agent, they are partial bearers of her cognitions, motivations, memories, and so on. According to proponents of the situationist challenge to virtue theory, dispositions located solely within the confines of the nervous system (central or peripheral) or even the skin of the agent to whom they are attributed typically do not meet the normative standards associated with either virtue or vice (moral, epistemic, or otherwise) because they are too susceptible to moderating external variables, such as mood modulators, ambient sensibilia, and social expectation signaling. We here draw on both of these literatures to formulate two novel views – the embedded and extended character hypotheses – according to which the vehicles of not just mental states but longer-lasting, wider-ranging, and normatively-evaluable agentic dispositions are sometimes located partially beyond the confines of the agent’s skin. (shrink)

In this paper, I discuss a subset of preferences in which a person desires the fulfillment of a choice they have made, even if it involves the violation of their desires, as in rape fantasies. I argue that such cases provide us with a unique insight into personal autonomy from a proceduralist standpoint. In its first part, I analyze some examples in light of Frankfurt's endorsement theory and argue that even when we cannot endorse a practical decision that involves (...) being violated, we nonetheless regard those cases as instances of autonomy. Therefore, autonomy does not necessarily require endorsement. Instead, I propose that the nature of the relevant highest-order volition dictates the procedure that should be established in one’s desire structure for its fulfillment. In the second part, I discuss how an agent may effectively consent to the violation of their decision by another person. Ordinary consent typically refers to actions but fails to communicate one's higher-order desires or commitments. To address this limitation, I propose a practical tool that accomplishes this by signaling shifts in the normative context where the agents are interacting. (shrink)

Essential Microeconomics is designed to help students deepen their understanding of the core theory of microeconomics. Unlike other texts, this book focuses on the most important ideas and does not attempt to be encyclopedic. Two-thirds of the textbook focuses on price theory. As well as taking a new look at standard equilibrium theory, there is extensive examination of equilibrium under uncertainty, the capital asset pricing model, and arbitrage pricing theory. Choice over time is given extensive coverage (...) and includes a basic introduction to control theory. The final third of the book, on game theory, provides a comprehensive introduction to models with asymmetric information. Topics such as auctions, signaling and mechanism design are made accessible to students who have a basic rather than a deep understanding of mathematics. Examples and diagrams are used to illustrate issues as well as formal derivations. (shrink)

Do people fall for online disinformation, or do they actively utilize it as a tool to accomplish their goals? Currently, the notion of the members of the public as victims of deception and manipulation prevails in the debate. It emphasizes the need to limit people’s exposure to falsehoods and bolster their deficient reasoning faculties. However, the observed epistemic irrationality can also stem from politically motivated reasoning incentivized by digital platforms. In this context, the readily available disinformation facilitates an arms race (...) in loyalty signaling via a public endorsement of fanciful partisan claims. Such a signaling arms race appears capable of derailing democratic decision-making perhaps more effectively than any known reasoning deficiency. Appreciating the role of an instrumentally rational cost-benefit calculus in triggering the disinformation crisis thus appears vital. Examining these themes, the paper contributes to the current debates in political epistemology and democratic theory. (shrink)

Slurs’ meaning is highly unstable. A slurring utterance like ‘Hey, F, where have you been?’ (where F is a slur) may receive a wide array of interpretations depending on various contextual factors such as the speaker’s social identity, their relationship to the target group, tone of voice, and more. Standard semantic, pragmatic, and non-content theories of slurs have proposed different mechanisms to account for some or all types of variability observed, but without providing a unified framework that allows us to (...) understand how different contextual factors simultaneously influence slurs’ interpretation. To address this issue, I argue that slurs convey dimensional qualities such as, e.g., ‘negative valence, neutral arousal, high dominance’ instead of discrete emotional categories such as ‘contempt’. Then, I translate this hypothesis into a game-theoretic model of slurs’ interpretation inspired by Heather Burnett’s pioneering work on identity construction. This new model, called ‘Affective Meaning Games’ (AMG), captures the variability of slurs and integrates pragmatic reasoning within an independently motivated psychological understanding of emotional states. (shrink)

How are fundamental constants, such as c for the speed of light, related to particular technological environments? Our understanding of the constant c and Einstein’s relativistic cosmology depended on key experiences and lessons learned in connection to new forms of telecommunications, first used by the military and later adapted for commercial purposes. Many of Einstein’s contemporaries understood his theory of relativity by reference to telecommunications, some referring to it as “signal-theory” and “message theory.” Prominent physicists who contributed (...) to it (Hans Reichenbach, Max Born, Paul Langevin, Louis de Broglie, and Léon Brillouin, among others) worked in radio units during WWI. At the time of its development, the old Newtonian mechanics was retrospectively rebranded as based on the belief in a means of “instantaneous signaling at a distance.” Even our thinking about lengths and solid bodies, argued Einstein and his interlocutors, needed to be overhauled in light of a new understanding of signaling possibilities. Pulling a rod from one side will not make the other end move at once, since relativity had shown that “this would be a signal that moves with infinite speed.” Einstein’s universe, where time and space dilated, where the shortest path between two points was often curved and which broke the laws of Euclidean geometry, functioned according to the rules of electromagnetic signal transmission. For some critics, the new understanding of the speed of light as an unsurpassable velocity—a fundamental tenet of Einstein’s theory—was a mere technological effect related to current limitations in communication technologies. (shrink)

HORMÔNIOS E SISTEMA ENDÓCRINO NA REPRODUÇÃO ANIMAL -/- OBJETIVO -/- As glândulas secretoras do corpo são estudadas pelo ramo da endocrinologia. O estudante de Veterinária e/ou Zootecnia que se preze, deverá entender os processos fisio-lógicos que interagem entre si para a estimulação das glândulas para a secreção de vários hormônios. -/- Os hormônios, dentro do animal, possuem inúmeras funções; sejam exercendo o papel sobre a nutrição, sobre a produção de leite e sobre a reprodução, os hormônios desempenham um primordial papel (...) quanto ao funcionamento do animal. -/- Nesse capítulo, o estudante identificará os hormônios relevantes para o controle reprodutivo, suas características e o uso clínico dos mesmos. -/- -/- INTRODUÇÃO -/- A endocrinologia é a ciência que se encarrega do estudo do sistema endócrino: um sistema de comunicação entre as células de um organismo; esse trabalho de comunicação é compartilhado com o sistema nervoso já que ambos sistemas possuem características distintas que lhes permite complementar-se para alcançar uma adequada coordenação das funções. Em algumas ocasiões o sistema nervoso e o sistema endócrino interagem direta-mente na transmissão de uma mensagem, pelo qual se conhece como sistema neuroendó-crino. -/- -/- OS HORMÔNIOS -/- A endocrinologia é a ciência que se encarrega do estudo dos hormônios e seus e-feitos. De maneira tradicional os hormônios são considerados como “substâncias secreta-das em direção a circulação pelas glândulas especializadas, e que exercem uma função sobre um órgão branco”. Essa definição, no entanto, é limitada e imprecisa. É necessário ser mais pontual, já que os hormônios não são produzidos em qualquer célula da glândula, senão nas células específicas. Por exemplo, o hormônio luteinizante (LH) é produzido pelos gonadotropos da adenohipófise e não por qualquer outro tipo de célula hipofisária. Da mesma maneira, falar de um “órgão branco” não é exato, já que os hormônios atuam somente nas células que tenham receptores específicos para esse hormônio, e não outras células do mesmo órgão; logo, falar de uma “célula branca” é mais apropriado que falar de um “órgão branco”. As células brancas do LH no testículo são as células de Leydig e as células brancas do hormônio folículo estimulante (FSH) no mesmo órgão são as células de Sertoli. -/- Mediante o supracitado, uma definição mais apropriada de hormônio é a seguinte: “Os hormônios são reguladores biológicos, produzidos e secretados em quantidades pe-quenas pelas células vivas, que depois de viajar pelo meio extracelular atuam sobre as cé-lulas brancas, onde exercem uma ação específica”. -/- É importante levar em conta que os hormônios somente regulam (estimulam ou inibem) funções que já existem na célula branca. Ademais, os hormônios são extraordina-riamente potentes, pelo qual se requerem quantidades muito pequenas para induzir uma resposta na célula. As concentrações circulantes da maioria dos hormônios estão na ordem de nanogramas (10-9 g) ou pictogramas (10-12 g) por mililitro. -/- Etimologicamente o termo “endócrino” significa “secretar em direção adentro”, já que os hormônios são secretados em direção ao interior do organismo (o sangue ou o espaço intracelular), em diferença das secreções exócrinas (em direção ao exterior), que são secretadas em direção a luz de um órgão, como o intestino no caso das enzimas pan-creáticas. -/- Algumas substâncias, sem deixar de ser hormônios, recebem uma classificação adicional em relação ao seu local de ação, ao tipo de células que lhes produzem, ou a al-guma outra característica. Agora, serão descritas algumas dessas características (figura 1). -/- -/- Parahormônio ou hormônio local -/- A maioria dos hormônios são transportados pela circulação desde seu local de se-creção até a célula branca. No entanto, alguns hormônios exercem seu efeito em células adjacentes aquelas que foram produzidos, ao qual não é necessário seu transporte através da circulação geral. Esse tipo de substâncias são chamadas de parahormônios ou hormô-nios locais, e sua liberação é denominada como secreção parácrina. Um exemplo é a pros-taglandina F2 alfa (PGF₂α), que é produzida no epitélio uterino (endométrio) e provoca as contrações nas células musculares do mesmo órgão (miométrio). Deve-se tomar em conta que a mesma substância poderia se comportar em outros casos como um hormônio clássico, atuando em um órgão distinto ao local de sua produção; é o caso da mesma PGF₂α de origem endometrial quando atua sobre as células do corpo lúteo do ovário, pro-vocando sua regressão. A classificação de uma substância como hormônio ou parahormô-nio não depende de sua estrutura química, senão da relação espacial existente entre a célu-la que o produz e a célula branca. -/- -/- Neurohormônio -/- A maioria dos hormônios são produzidos pelas células de origem epitelial, porém, muitos deles são produtos pelos neurônios, logo denominados como neurohormônios. To-dos os neurônios segregam alguma substância, porém tratam-se dos neurohormônios quando o neurônio que os produz despeja-os diretamente em direção a circulação geral, através da qual chegam aos órgãos para exercer seu efeito, sejam na indução, inibição ou estimulação do mesmo. -/- Esse processo é diferente dos neurotransmissores, os quais também são secretados por um neurônio, mas exercem seu efeito em uma célula adjacente com o qual o neurônio estabelece uma sinapse (neuroma com neurônio, neurônio com célula muscular, neurônio com célula glandular). A classificação de uma substância como hormônio ou como neuro-hormônio não depende de sua estrutura química, senão do tipo de célula que o produz. Uma mesma substância é um hormônio quando ele é produzido por uma célula epitelial e um neurohormônio se é produzido por um neurônio. A ocitocina, por exemplo, é secre-tada na neurohipófise por neurônios hipotalâmicos, nesse caso se trata de um neurohor-mônio, mas também é secretada por células do corpo lúteo dos ruminantes, e se trata nesse caso, de um hormônio. A distinção entre um neurohormônio e um hormônio é um neuro-transmissor, da mesma forma, não depende de sua estrutura química, e sim do local onde é secretado. Por exemplo, a dopamina atua como neurotransmissor quando se libera em sinapse da substância negra do mesencéfalo z mas atua como neurohormônio quando é liberada por neurônios hipotalâmicos em direção a circulação do eixo hipotálamo-hipofisário. -/- -/- Pré-hormônio -/- Em alguns casos, os hormônios são secretados em forma inativa (pré-hormônio), que requer uma transformação posterior para converter-se na forma ativa de hormônio. O angiotensinógeno circulante somente cobrará atividade biológica ao se transformar em angiotensina por ação da enzima renina. Algumas substâncias podem atuar como hormô-nios m alguns casos e como pré-hormônios em outros. A testosterona, por exemplo, atua como hormônio nas células musculares, aos quais possui um efeito anabólico direto. O certo é que para a testosterona induzir a masculinização dos órgãos genitais externos em um efeito macho é necessário que seja transformada previamente em 5α-di-hidrotes-tosterona pela enzima 5α-redutase presente nas células de tecido branco, por onde, nesse caso a testosterona é um pré-hormônio de di-hidrotestosterona. -/- -/- Feromônio -/- Os hormônios são mensagens químicas que comunicam a células distintas dentro do mesmo organismo, embora existam casos aos que requerem uma comunicação quími-ca entre organismos diferentes, em geral da mesma espécie. As substâncias empregadas para esse fim denominam-se feromônios. Essas substâncias devem possuir a capacidade de dispersão sobre o ambiente, pelo que nos organismos terrestres geralmente trata-se de substâncias voláteis, enquanto que os feromônios de organismos aquáticos geralmente são substâncias hidrossolúveis. Embora muitos feromônios possuam uma função sexual ou reprodutiva como é o caso de muitas espécies como a canina em que a fêmea em cio dispersa grandes quantidades de feromônios que são captados de longe pelos machos, todavia esse não é sempre o caso, e eles podem ser utilizados para outros tipos de comunicação, como é o caso dos feromônios utilizados pelas formigas para sinalização da rota em direção a fonte de alimentação. E como as abelhas no sentido de orientação da fonte de pólen até a colmeia. Muitos desses feromônios podem ser artificializados, isto é, elaborados pelo homem em laboratório para o estudo ou manipulação de algum animal. -/- -/- O SISTEMA ENDÓCRINO COMO UM SISTEMA DE COMUNICAÇÃO -/- O sistema endócrino é um sistema de comunicação que tem como objetivo coor-denar as funções das células de diferentes órgãos para mantença da homeostase do orga-nismo e promover seu desenvolvimento, crescimento e reprodução. Também ajuda os or-ganismos a adaptarem-se as mudanças de ambiente e ao habitat. O sistema endócrino representa um sistema de comunicação do tipo sem fio, diferentemente do sistema nervo-so que é um sistema de comunicação com fio. -/- Em todo o sistema de comunicação existe uma série de elementos que são necessá-rios para a realização da comunicação de forma efetiva. Esses elementos incluem o emis-sor, a mensagem, o sinal, o meio de transporte do sinal, o receptor, o efetor, a resposta e o feedback ou retroalimentação (figura 1). Todos os elementos são igualmente importan-tes e uma deficiência em qualquer deles pode interromper ou alterar a comunicação. -/- -/- Figura 1: componentes do sistema endócrino de comunicação. Fonte: ZARCO, 2018. -/- -/- Emissor ou transmissor -/- É o elemento responsável pela transmissão de uma mensagem; poderíamos com-pará-lo com a redação de notícias de um canal de televisão. Antes de decidir quais serão as notícias que serão transmitidas esse dia, em que ordem se apresentarão e que ênfase lhes darão, as pessoas da redação analisa rodas as informações disponíveis: provenientes de seus repórteres, de agências de notícias internacionais, publicada em jornais do dia, a existente na internet ou disponíveis através de redes sociais; isso significa que as mensa-gens transmitidas pelo emissor não são aleatórias, e sim respondem a uma análise respon-sável das necessidades de informação. -/- No sistema endócrino o emissor é a célula que produz e secreta um hormônio. Co-mo todo emissor responsável, a mesma célula analisa toda a informação relevante dispo-nível, tal como a concentração de diversos metabólitos no sangue, a concentração de ou-tros hormônios, e as mensagens que recebem por via nervosa, antes de decidir se secretará seu hormônio, em que quantidade o fará e com que frequência. Por essa razão, ao estudar o sistema endócrino não somente devemos conhecer a célula transmissora, e sim qual é a informação que a célula pode receber, e como a analisa e a prioriza para construir sua mensagem. -/- -/- Mensagem -/- É a informação transmitida pelo emissor. No caso de um sistema de notícias tele-visivas a mensagem é a notícia, por exemplo “Vaca dá a luz trigêmeos, um caso raro no Brasil”. No sistema endócrino a mensagem que se transmite é uma instrução para que em outra célula se realize determinadas ações. Por exemplo, os neurônios produtores de GnRH no hipotálamo de uma coelha, ao analisar as concentrações de estradiol circulantes e a informação nervosa procedente de neurônios sensoriais nós órgãos genitais da fêmea, podem “saber” que nos ovários existam folículos lisos para ovularem e que a coelha está copulando, pelo qual decidem transmitir a mensagem “Solicita-se os gonadotropos da adenohipófise a liberação de LH em quantidade suficiente para provocar a ovulação”. -/- -/- Sinal -/- É a forma a qual se codifica a mensagem para permitir sua difusão. No caso de um jornal, a mensagem (por exemplo a notícia da vaca que deu a luz trigêmeos) se codifi-ca em forma de ondas de rádio de uma determinada frequência, amplitude e intensidade; no caso do sistema endócrino a mensagem (a necessidade de realizar uma função celular) é codificada em forma de hormônio secretado em determinada quantidade, frequência e amplitude. Para o exemplo descrito supra, a mensagem se codifica na forma de uma grande elevação nas concentrações de GnRH no sangue do sistema porta hipotálamo-hipofisário. -/- É necessário tomar em conta que o emissor codifica a mensagem de forma tal que quando o receptor decifre o sinal obtenha a informação originalmente contida na mensa-gem. No entanto, o sinal pode ser interpretado de diferentes formas por receptores distintos, o que pode provocar respostas contrárias as esperadas. A notícia transmitida por um jornal de rádio, por exemplo, poderia estar codificada em forma de ondas de rádio que, casualmente, para o sistema eletrônico de um avião signifiquem “baixe a altitude e acelere”, razão pela qual é proibido utilizar aparelhos eletrônicos durante a decolagem e aterrissagem desses aparelhos. -/- Do mesmo modo, a mensagem codificada na forma de secreção de estradiol por parte dos ovários pode ser interpretado pelo sistema nervoso de uma ovelha como uma ordem para apresentar conduta de estro, pelas células do folículo ovariano como uma instrução para sofrer mitose e secretar o líquido folicular, pelos gonadotropos como uma ordem para a secreção de um pico pré-ovulatório de LH, e pelas células do endométrio como uma instrução para sintetizar receptores para a ocitocina. Dessa forma, o mesmo sinal (secreção de estradiol) pode conter diferentes mensagens para diferentes células do organismo. -/- Em alguns casos, pode-se apresentar uma resposta patológica devido as diversas formas de interpretação de uma mensagem, por exemplo, a repetição da secreção de adrenalina em um indivíduo estressado pode resultar no desenvolvimento de um proble-ma de hipertensão arterial. Por isso é necessário conhecer a maneira em que cada célula endócrina codifica suas mensagens, assim como a forma em que esses sinais podem ser interpretados em diferentes órgãos e tecidos, em diferentes momentos da vida do animal, em animais com diferentes antecedentes de espécies diferentes. -/- -/- Meio de transporte do sinal -/- O sinal tem que viajar ou difundir-se desde o emissor até o receptor, e em seu ca-minho pode ser modificado de diversas formas. Os sinais de rádio, por exemplo, viajam através da atmosfera e durante esse trajeto podem ser bloqueados por uma barreira física (como ocorre com as ondas de rádio AM em um túnel), ampliadas por uma estação repeti-dora, alteradas por um campo eletromagnético (uma aspiradora funcionando ao lado da sala de transmissão), entre outros. Da mesma forma, os sinais endócrinos que geralmente viajam no sangue, podem ser modificados ao longo do seu caminho. -/- A PGF₂α é inativada ao passar pelo pulmão, o angiotensinógeno é ativado pela re-nina na circulação, e a testosterona pode ser transformada em di-hidrotestosterona nas células da pele e na próstata, ou em estrógenos nos adipócitos e nos neurônios. Por tudo isso, o sinal que finalmente chega ao receptor pode ser diferente do transmitido pelo emissor. -/- Portanto, ao estudar qualquer sistema hormonal devemos conhecer as possíveis modificações que o hormônio pode sofrer desde o momento em que é secretado até que se uma ao seu receptor na célula branca. -/- -/- Receptor -/- É o elemento que recebe o sinal e interpreta a mensagem contida nele. No caso de um jornal de TV, o receptor é o canal correspondente (por exemplo o canal 2) em um aparelho de televisão. É importante ressaltar que um aparelho de TV possui muitos canais distintos, mas somente receberá mensagens se estiver ligado e sintonizado no canal que está transmitindo a mensagem de interesse. Ou seja, o receptor tem que estar ativo. -/- No caso das mensagens endócrinas os receptores são moléculas específicas nas células brancas. Essas moléculas são proteínas membranais ou citoplasmáticas (segundo o tipo de hormônio), que possui uma alta afinidade por seu hormônio, o que lhes permite registrar a mensagem apenas das baixíssimas concentrações em que os hormônios circu-lam. Os receptores possuem uma alta especificidade, o que significa que somente se unem a seu próprio hormônio, e não a outras substâncias. Em algumas ocasiões um receptor pode receber diversos hormônios do mesmo tipo; por exemplo o receptor de andrógenos pode unir testosterona, androstenediona, di-hidrotestosterona e diversos andrógenos sin-téticos. Apesar disso, cada um desses hormônios pode possuir uma afinidade diferente pelo receptor, pelo qual alguns serão mais potentes que outros para estimulação. -/- Em geral existe um número limitado de moléculas receptoras em cada célula, logo diz-se que os receptores são “saturáveis”, o qual significa que uma vez que todos sejam ocupados a célula não pode receber mais moléculas desse hormônio. Por essa razão a magnitude da resposta de um determinado hormônio vai aumentando conforme se aumen-tam suas concentrações, porém ao saturar-se os receptores alcançam um ponto em que a resposta já não aumenta embora sigam incrementando as concentrações hormonais já que os receptores não permanecem livres para unirem-se ao excesso de moléculas do hormô-nio. -/- As células, em contrapartida, podem regular tanto o número de receptores presen-tes como a afinidade destes por seu hormônio; isso significa que a magnitude da resposta antes um determinado sinal endócrino pode ser distinta em diferentes momentos da vida de um animal; depende do estado dos receptores presentes nos tecidos, pelo qual é impor-tante conhecer quais são os fatores que podem aumentar ou reduzir o número de recepto-res em uma célula, assim como aqueles que podem aumentar ou diminuir a afinidade des-ses receptores por seus hormônios. -/- -/- Efetor -/- É o elemento encarregado de responder a uma mensagem realizando uma ação, e é um elemento diferente do receptor. Vale ressaltar que no caso de uma transmissão de televisão o receptor é o aparelho sintonizado no canal de interesse, porém o efetor é o te-lespectador que está exposto as notícias. Esse telespectador sofrerá mudanças que podem resultar em uma ação. A mudança pode ser evidente (e auxiliar as vítimas de um desastre), ou simplesmente uma mudança potencial (ao se inteirar de uma notícia não se pode produ-zir nenhuma mudança aparente até que alguém lhe pergunte: já se interessou?, E nesse caso a resposta será: “sim” em lugar do “não”). Deve-se tomar em conta que o efetor pode estar ausente embora o receptor esteja presente (um televisor ligado em uma sala vazia). O efetor também pode estar inativado (o telespectador encontra-se dormindo); quando assim ocorre não irá produzir uma resposta embora o receptor esteja presente. -/- No sistema endócrino o efetor é, em geral, um sistema celular encarregado de rea-lizar uma determinada função. Na maioria dos casos trata-se de sistemas enzimáticos cuja função é estimulada pela união do hormônio ao seu receptor. Alguns hormônios, por exemplo, atuam através do sistema AMP cíclico (AMPc) logo, a união do hormônio ao seu receptor resulta na ativação de uma proteína chamada Proteína Gs, que ativa a enzima Adenil-ciclase (ou adenilato ciclase), a qual transforma ATP em AMPc. A presença de AMPc resulta na ativação de uma enzima cinese de proteínas que fosforiza outras enzi-mas, o que pode ativá-las ou inativá-las; nesses casos, é gerada uma cascata de eventos que resulta em uma mudança na atividade celular; por exemplo, a cadeia de eventos que produz-se em resposta ao AMPc quando a célula de Leydig do testículo é estimulada pela união do LH a seu receptor resulta na produção de testosterona, enquanto que a estimula-ção de um adipócito provocada pela união da adrenalina a seu receptor, que também atua através do sistema AMPc, resulta em uma série de eventos que provocam, finalmente, a liberação de ácidos graxos livres em direção a circulação. -/- Nos exemplos supra, o AMPc é considerado um mensageiro intracelular, já que o receptor capta o sinal (hormônio) no exterior da célula, o que resulta na produção de um novo sinal (mudança nas concentrações de AMPc) no interior da célula. Embora o sistema AMPc seja utilizado por muitos hormônios, não é um sistema universal; existem outros sistemas mensageiros intracelulares que também são utilizados para responder os hormô-nios que não entram nas células, por exemplo o sistema cálcio-calmodulina, ou os siste-mas baseados em receptores com atividade de cineses de tirosina. Nos casos que os hor-mônios possa atravessar livremente a membrana celular, como acontece com os hormôni-os esteroides, o hormônio se une a receptores presentes no citoplasma, que depois ingres-sam ao núcleo celular para intervir na regulação da transcrição do genoma. -/- De maneira independente ao mecanismo de ação de um determinado hormônio, sua presença finalmente desencadeará mudanças em um ou mais sistemas efetores da célula, o que permitirá que a mesma responda a mensagem que o emissor transmitiu originalmente. É evidente que para compreender a ação de qualquer hormônio é indispensável conhecer seu mecanismo de ação, o papel dos mensageiros intracelulares e as característi-cas dos sistemas efetores. Deve-se conhecer também quais são os fatores que afetam a transdução da mensagem já que uma célula pode regular seus sistemas efetores e dessa forma ter uma resposta maior, menor ou alterada ante a mesma mensagem. -/- -/- Resposta -/- Como mencionado, qualquer mensagem provoca uma resposta (embora somente seja potencial) sobre o efetor que a recebe. No sistema endócrino, as mensagens hormonais viajam constantemente pelo organismo e são captadas por todas as células que possuem receptores ativos para um determinado hormônio. Uma única célula pode ter receptores para diferentes hormônios, pelo qual pode estar recebendo diversas mensagens simultaneamente, e cada uma dessas mensagens pode afetar a resposta de outras mensagens. Por exemplo, a presença de progesterona pode alterar a resposta das células endometriais ao estradiol. Ademais, as células podem estar recebendo ao mesmo tempo uma informação não hormonal, como as concentrações de diversos metabólitos na circulação, ou a recebida pelo sistema nervoso. A célula analisa toda essa informação e com base nela decide se deve responder a mensagem hormonal que está recebendo como deve responder, com que intensidade e durante quanto tempo. A resposta final pode ser uma resposta física imediata (contração, secreção de um hormônio armazenado previa-mente), uma modificação bioquímica a curto prazo (síntese de um determinado hormônio ou outra substância), ou o início de uma série de mudanças que levam a uma mudança a longo prazo (divisão celular, diferenciação celular, crescimento, morte celular). -/- -/- Feedback ou retroalimentação -/- Quando em um sistema de comunicação se produz uma resposta, em muitos casos essa resposta engloba a geração de informação que vai retornar ao emissor, e que agora constituirá um ou mais dos elementos que o emissor tomará em conta antes de transmitir uma nova mensagem. Assim, se um jornal transmite uma mensagem “menina pobre necessita de doação de roupas”, a resposta de alguns efetores (telespectadores) que virão a doar roupas será conhecida pelo emissor, que assim saberá que já não será mais neces-sário voltar a transmitir a mensagem, o que o fará tomar a decisão de transmitir uma mensagem diferente como “menina pobre já não necessita de roupas, porém requer de ali-mentos para sua família”. Essa modificação da mensagem provocada pela resposta do efetor é conhecida como retroalimentação. -/- De forma análoga, no sistema endócrino a resposta da célula efetora geralmente é reconhecida pelo emissor, que em consequência modifica sua mensagem. Na maioria dos casos se produz uma retroalimentação negativa, que consiste em que a resposta do efetor provoca uma redução na intensidade da mensagem transmitida pelo emissor. Quando os gonadotropos de uma vaca secretam hormônio folículo estimulante (FSH), as células da granulosa de seus folículos ovarianos respondem realizando diversas funções, uma das quais é a secreção de inibina. A elevação nas concentrações circulantes de inibina é capta-da pelos gonadotropos, que logo sabem que o FSH já transmitiu sua mensagem, pelo que reduzem a secreção deste hormônio. A retroalimentação negativa é muito importante em qualquer sistema endócrino já que permite manter as concentrações hormonais dentro de limites aceitáveis. -/- A retroalimentação negativa pode ser de onda ultracurta, curta ou longa. A onda ultracurta é quando o hormônio produzido por uma célula pode inibir sua própria secre-ção. A retroalimentação negativa de onda curta é quando o hormônio produzido por uma célula pode inibir a de um órgão imediatamente superior na hierarquia (por exemplo, quando a progesterona produzida pelo corpo lúteo do ovário inibe a secreção de LH pelos gonadotropos da hipófise). O feedback negativo de onda longa sucede quando o hormônio produzido por uma célula inibe a uma célula de um órgão que está dois ou mais níveis por cima na escala hierárquica, por exemplo, quando a testosterona produzida pelas células de Leydig do testículo inibe diretamente os neurônios produtores de GnRH, saltando as células produtoras de LH e adenohipófise. -/- Existe também a retroalimentação positiva, da qual o primeiro hormônio estimula a secreção de um segundo hormônio, o que por sua vez estimula o primeiro, com o que se estabelece um círculo progressivo de estimulação. Um exemplo de retroalimentação positiva é a que se produz pouco antes da ovulação entre o LH hipofisário e o estradiol de origem folicular. Os dois hormônios se estimulam mutuamente até que alcancem níveis elevados de LH que provoca a ovulação. O círculo de feedback positivo termina quando o pico pré-ovulatório de LH mudanças sobre o folículo que incluem a perda da capacidade de produção de estrógenos. Todo o sistema de retroalimentação positiva deve ter um final abrupto sobre o qual se rompe o ciclo de estimulação mútua, já que não mais deverá ser produzida quantidades elevadas dos hormônios, até que todos os recursos do organismo sejam utilizados para esse fim. -/- -/- CLASSIFICAÇÃO QUÍMICA DOS HORMÔNIOS -/- Do ponto de vista químico e sobre o estudo da Fisiologia da Reprodução Animal, existem quatro grupos principais de hormônios: polipeptídios, esteroides, aminas e prostaglandinas; dentro de cada grupo, por sua vez, existem mais grupos de inúmeros outros hormônios dispostos em subdivisões. -/- -/- Hormônios polipeptídios -/- Os polipeptídios são cadeias de aminoácidos. Quando uma dessas cadeias está constituída por poucos aminoácidos é denominada simplesmente de polipeptídios, mas quando uma cadeia de aminoácidos é longa e adquire uma configuração espacial de três dimensões o polipeptídio é denominado proteína (figura 2). Muitos neurohormônios hipo-talâmicos são polipeptídios, como o liberador de gonadotropinas (GnRH), constituído por 10 aminoácidos, o hormônio liberador de tirotropina (TRH), formado por 3 aminoácidos, o somatostatina, constituído por 14 aminoácidos, a ocitocina que é formada por 8 aminoá-cidos etc. O sistema nervoso central e a hipófise produzem peptídeos opioides. -/- Entre os hormônios polipeptídios que por seu tamanho são considerados proteínas encontramos a prolactina, o hormônio do crescimento, os lactogênios placentários, a relaxina, a insulina e fatores de crescimento parecidos com a insulina (IGFs). Existe outro grupo de hormônios polipeptídios classificados como glicoproteínas. Trata-se de proteí-nas que possuem carboidratos unidos a alguns de seus aminoácidos. -/- -/- Figura 2: classificação dos hormônios polipeptídios. Fonte: ZARCO, 2018. -/- -/- Há um grupo de hormônios glicoproteicos que constituem uma família de molécu-las similares entre si, dentro das quais estão o hormônio luteinizante (LH), o hormônio folículo estimulante (FSH), o hormônio estimulante da tireoide (TSH), a gonadotropina coriônica humana (hCG) e a gonadotropina coriônica equina (eCG); todos estão formados pela subunidade alfa que é idêntica para os hormônios de uma determinada espécie animal, e por uma subunidade beta específica para cada hormônio. As duas subunidades mantém-se unidas através de ligações dissulfeto. Deve-se mencionar que os carboidratos associados as glicoproteínas podem ser distintos em diferentes idades, épocas do ano ou estados fisiológicos; esse processo é conhecido como microheterogenicidade, e recente-mente têm-se dado grande importância a seu estudo, já que é reconhecido fatores tais como a vida média de um hormônio ou sua atividade biológica podem ser modificados de acordo com o tipo de carboidratos presentes na molécula. -/- Existe outra família de hormônios glicoproteicos, que incluem a inibina A, a B, e a activina A, AB e B. Todos os hormônios polipeptídios possuem algumas características comuns. Em primeiro lugar, trata-se de moléculas hidrossolúveis que não conseguem atravessar as membranas celulares pelo qual se unem a receptores transmembranais que flutuam sobre a parede externa da membrana da célula branca e requerem de um segundo mensageiro intracelular, como o cálcio ou o AMPc, para levar sua mensagem ao interior da célula. -/- Os hormônios desse grupo, não podem ser administrados por via dérmica, oral, retal ou intravaginal, já que não podem atravessar a pela ou as mucosas intestinais, retais ou vaginais. Os polipeptídios são digeridos no estômago, o que também impede sua admi-nistração oral. Outra característica que deve-se tomar em conta é que as proteínas (embora não os polipeptídios pequenos) podem se desnaturalizar por fatores como o calor (são termolábeis), a congelação, ou mudanças de pH m a desnaturalização consiste em uma mudança na forma natural da proteína, o que leva a perda de sua função. Por essa razão, ao trabalhar com hormônios proteicos devem-se tomar cuidados especiais durante seu manejo para evitar a exposição a fatores desnaturalizantes. -/- -/- Hormônios esteroides -/- São moléculas derivadas do colesterol; a célula esteroidogênica pode sintetizar o colesterol, obtê-lo de reservas intracelulares ou da circulação. Na célula esteroidogênica existem diversas enzimas que atuam sequencialmente sobre a molécula de colesterol, provocando mudanças sucessivas até obter o hormônio final que será secretado, ao qual dependerá das enzimas que estão presentes e ativas na célula. -/- Existem cinco grupos principais de hormônios esteroides; os progestágenos, os estrógenos, os glicocorticoides e os mineralocorticoides (figura 3). -/- Os progestágenos são hormônios que favorecem o desenvolvimento da gestação; seus efeitos incluem, entre outros, a estimulação da secreção endometrial de substâncias nutritivas para o embrião, a estimulação do desenvolvimento embrionário e placentário, a inibição das contrações uterinas, bem como fazer com que a cérvix fique fechada. O principal hormônio natural desse grupo é a progesterona, mas existem uma grande quantidade de progestágenos sintéticos utilizados na medicina veterinária, tais como o acetato fluorogestona (FGA), o acetato de melengestrol (MGA), o altrenogest e o norgestomet. -/- Os estrógenos são os hormônios femininos responsáveis, entre outras funções, dos sinais do estro ou receptividade sexual nas fêmeas. A maior parte de seus efeitos estão no alcance da fertilização do ovócito. Os estrógenos, além de estimular a conduta sexual feminina, favorecem, entre outras coisas, a abertura da cérvix para permitir a passagem do espermatozoide, e as contrações uterinas para impulsionar o sêmen em direção aos ovidutos. O principal estrógeno natural é o estradiol 17β, outros membros naturais do grupo são a estrona, a equilina e a equilenina, esses dois últimos presentes exclusivamente em éguas gestantes. Também existem numerosos estrógenos sintéticos, tais como o valerato de estradiol, o benzoato de estradiol e o cipionato de estradiol. -/- Os andrógenos são hormônios masculinos. Possuem uma grande quantidade de efeitos encaminhados a alcançar o êxito reprodutivo do macho, como estimular a conduta sexual, estimular a produção de espermatozoides e estimular as secreções das glândulas sexuais acessórias. O andrógeno principal é a testosterona, outros andrógenos naturais incluem a androstenediona e a di-hidrotestosterona. Existe também inúmeros andrógenos sintéticos. -/- Os glicocorticoides ou corticosteroides possuem funções principalmente metabó-licas e de adaptação ao estresse. O principal corticosteroide na maioria das espécies é o cortisol, enquanto que nos ratos e outros roedores é a corticosterona. Na reprodução, os corticosteroides desempenham um papel relevante, em particular durante o parto e a lac-tação. -/- Os mineralocorticoides, como a aldotestosterona, se encarregam da regulação do balanço de líquidos e eletrólitos no organismo. -/- -/- Figura 3: subgrupos dos hormônios esteroides. Fonte: ZARCO, 2018. -/- -/- Os hormônios esteroides como grupos são hidrossolúveis, pelo qual podem atra-vessar livremente as membranas celulares, por essa razão utilizam receptores intracelula-res que se encontram no citoplasma da célula branca; também pode-se administrar por via oral, pela pele, e através das mucosas retal ou vaginal. São moléculas termoestáveis e não são digeridas no estômago, embora algumas possas sofrer modificações na pH ácido, alterando sua função. -/- -/- Aminas -/- São moléculas derivadas de um aminoácido que se modifica pela ação de enzimas específicas. Existem dois tipos de hormônios aminas: as catecolaminas e as indolaminas (figura 4). As catecolaminas derivam do aminoácido tirosina, e incluem a dopamina, a a-drenalina e a noradrenalina. As indolaminas derivam-se do triptofano, e incluem a seroto-nina e a melatonina. -/- As aminas são moléculas hidrossolúveis que não podem atravessar as membranas celulares e portanto atuam através de receptores membranais e segundos mensageiros intracelulares. -/- -/- Figura 4: classificação dos hormônios peptídicos. Fonte: ZARCO, 2018. -/- -/- Prostaglandinas -/- São substâncias derivadas do ácido araquidônico. A principal fonte desse ácido graxo são os fosfolipídios da membrana celular, a partir dos quais se podem liberar o ácido araquidônico mediante a ação da enzima fosfolipase A2. O ácido araquidônico se transforma em prostaglandina H mediante a ação da enzima ciclo-oxigenase (ou sintetase de prostaglandinas), que mais adiante se transforma em diferentes prostaglandinas especí-ficas pela ação de diversas enzimas. O tipo de prostaglandina produzido por cada célula dependerá do complemento de enzimas presentes. -/- A prostaglandina mais importante na reprodução é a PGF2α, a qual é responsável pela destruição do corpo lúteo na maioria das espécies; também provoca contrações uteri-nas, pelo qual é importante para o parto, e o transporte dos espermatozoides e a involução uterina depois do parto. Na prática veterinária a PGF2α natural (dinoprosr) ou seus seme-lhantes sintéticos (cloprostenol, luprostiol etc.) são utilizados para a sincronização do ciclo estral, para a indução do parto e para tratar diversas patologias. Outra prostaglandina com algumas ações relacionadas com a reprodução é a prostaglandina E2 (PGE2). -/- As prostaglandinas são substâncias anfipáticas (com propriedades hidrossolúveis e lipossolúveis), pelo qual podem atravessar as membranas celulares. -/- REFERÊNCIAS BIBLIOGRÁFICAS -/- AUSTIN, Colin Russell; SHORT, R. Reproduction in mammals. Cambridge, 1972. -/- BEARDEN, Henry Joe et al. Reproducción animal aplicada. México: Manual Moderno, 1982. -/- BECKER, Jill B. et al. (Ed.). Behavioral endocrinology. Mit Press, 2002. -/- BITTAR, Edward (Ed.). Reproductive endocrinology and biology. Elsevier, 1998. -/- BURNSTEIN, Kerry L. (Ed.). Steroid hormones and cell cycle regulation. Kluwer Academic Pub., 2002. -/- CUNNINGHAM, James. Tratado de fisiologia veterinária. Elsevier Health Sciences, 2011. -/- CUPPS, Perry T. (Ed.). Reproduction in domestic animals. Elsevier, 1991. -/- DUKES, Henry Hugh; SWENSON, Melvin J.; REECE, William O. Dukes fisiologia dos animais domésticos. Editora Guanabara Koogan, 1996. -/- FELDMAN, Edward C. et al. Canine and feline endocrinology-e-book. Elsevier health sciences, 2014. -/- FUSCO, Giuseppe; MINELLI, Alessandro. The Biology of Reproduction. Cambridge University Press, 2019. -/- GILBERT, Scott F. Biologia del desarrollo. Ed. Médica Panamericana, 2005. -/- GORE, Andrea C. GnRH: the master molecule of reproduction. Springer Science & Business Media, 2002. -/- HAFEZ, Elsayed Saad Eldin; HAFEZ, Bahaa. Reprodução animal. São Paulo: Manole, 2004. -/- HERNÁNDEZ PARDO, Blanca. Endocrinología: Lo esencial de un vistazo. México: Panamericana, 2016. -/- HYTTEL, Poul; SINOWATZ, Fred; VEJLSTED, Morten. Embriologia veterinária. São Paulo: Elsevier Brasil, 2012. -/- ILLERA MARTIN, Mariano. Endocrinología veterinaria y fisiología de la reproducción. Madrid: COLIBAC, 1984. -/- JOHNSON, Martin H. Essential reproduction. Nova Jersey: John Wiley & Sons, 2018. -/- MANDOKI, Juan José et al. Hormone multifunctionalities: a theory of endocrine signaling, command and control. Progress in biophysics and molecular biology, v. 86, n. 3, p. 353-377, 2004. -/- MANDOKI, Juan José et al. Reflections on the mode of functioning of endocrine systems. Archives of medical research, v. 41, n. 8, p. 653-657, 2010. -/- MCKINNON, Angus O. et al. (Ed.). Equine reproduction. Nova Jersey: John Wiley & Sons, 2011. -/- MELMED, Shlomo (Ed.). The pituitary. Londres: Academic press, 2010. -/- NORRIS, David O.; LOPEZ, Kristin H. (Ed.). Hormones and reproduction of vertebrates. Academic Press, 2010. -/- PARHAR, Ishwar S. (Ed.). Gonadotropin-releasing hormone: molecules and receptors. Elsevier, 2002. -/- PIMENTEL, C. A. Fisiologia e endocrinologia da reprodução da fêmea bovina. I Simpósio de Reprodução de Bovinos, Porto Alegre, RS, 2002. -/- PINEDA, Mauricio H. et al. McDonald's veterinary endocrinology and reproduction. Iowa state press, 2003. -/- RAMOS DUEÑAS, J. I. Endocrinología de la reproducción animal. 2018. -/- SALISBURY, Glenn Wade et al. Physiology of reproduction and artificial insemination of cattle. WH Freeman and Company., 1978. -/- SANDERS, Stephan. Endocrine and reproductive systems. Elsevier Health Sciences, 2003. -/- SORENSEN, Anton Marinus. Reproducción animal: principios y prácticas. México, 1982. -/- SQUIRES, E. James. Applied animal endocrinology. Cambridge: Cabi, 2010. -/- YEN, Samuel SC; JAFFE, Robert B.; BARBIERI, Robert L. Endocrinología de la Reproducción. Fisiología, fisiopatología y manejo clínico. Madrid: Ed. Médica Panamericana, 2001. -/- ZARCO, L. Endocrinología. In. PORTA, L. R.; MEDRANO, J. H. H. Fisiología reproductiva de los animales domésticos. Cidade do México: FMVZ-UNAM, 2018. (shrink)

Eating is a fundamental behavior in which all organisms must engage in order to procure the material and energy from their environment that they need to maintain themselves. Since controlling eating requires procuring, processing, and assessing information, it constitutes a cognitive activity that provides a productive domain for pursuing cognitive biology as proposed by Ladislav Kováč. In agreement with Kováč, we argue that cognition is fundamentally grounded in chemical signaling and processing. To support this thesis, we adopt Cisek’s strategy (...) of phylogenetic refinement, focusing on two animal phyla, Porifera and Placozoa, organisms that do not have neurons, muscles, or an alimentary canal, but nonetheless need to coordinate the activity of cells of multiple types in order to eat. We review what research has revealed so far about how these animals gather and process information to control their eating behavior. (shrink)

The articles in this issue represent the pursuit of a new understanding of the human past, one that can replace the neo-saltationist view of a human revolution with models that can account for the complexities of the archaeological record and of human social lives. The articulation of archaeological, philosophical, and biological perspectives seems to offer a strong foundation for exploring available evidence, and this was the rationale for collecting these particular articles. Even at this preliminary stage there is a coherence (...) emerging in proposals: the origin and operation of symbolically rich, complexly signaling human social systems was the consequence of the long-term evolution of multiple components of perceiving and negotiating social interactions, a contingent outcome of myriad adaptive shifts rather than a single event. (shrink)

One might think that if the majority of virtue signallers judge that a proposition is true, then there is significant evidence for the truth of that proposition. Given the Condorcet Jury Theorem, individual virtue signallers need not be very reliable for the majority judgment to be very likely to be correct. Thus, even people who are skeptical of the judgments of individual virtue signallers should think that if a majority of them judge that a proposition is true, then that provides (...) significant evidence that the proposition is true. We argue that this is mistaken. Various empirical studies converge on the following point: humans are very conformist in the contexts in which virtue signalling occurs. And stereotypical virtue signallers are even more conformist in such contexts. So we should be skeptical of the claim that virtue signallers are sufficiently independent for the Condorcet Jury Theorem to apply. We do not seek to decisively rule out the relevant application of the Condorcet Jury Theorem. But we do show that careful consideration of the available evidence should make us very skeptical of that application. Consequently, a defense of virtue signalling would need to engage with these findings and show that despite our strong tendencies for conformism, our judgements are sufficiently independent for the Condorcet Jury Theorem to apply. This suggests new directions for the debate about the epistemology of virtue signalling. (shrink)

Various writers have attempted to use the sender-receiver formalism to account for the representational capacities of biological systems. This paper has two goals. First, I argue that the sender-receiver approach to representation cannot be complete. The mammalian circadian system represents the time of day, yet it does not control circadian behaviours by producing signals with time of day content. Informative signalling need not be the basis of our most basic representational capacities. Second, I argue that representational capacities are primarily about (...) control, and only when specific conditions obtain does this control require informative signalling. (shrink)

One of the moral questions concerning autonomous vehicles (henceforth AVs) is the choice between types that differ in their built-in algorithms for dealing with rare situations of unavoidable lethal collision. It does not appear to be possible to avoid questions about how these algorithms should be designed. We present the results of our study of moral preferences (N = 2769) with respect to three types of AVs: (1) selfish, which protects the lives of passenger(s) over any number of bystanders; (2) (...) altruistic, which minimizes the number of casualties, even if this leads to death of passenger(s); and (3) conservative, which abstains from interfering in such situations. We differentiate between scenarios in which participants are to make their decisions privately or publicly, and for themselves or for their offspring. We aim to answer two research questions: (1) whether the public visibility of the choice of an AV type choice make this choice more altruistic and (2) which type of situation makes it more difficult to choose altruistically: when choosing for society as a whole, when choosing only for oneself, or when choosing only for one’s offspring. Our results show that respondents exhibit a preference for an altruistic strategy for AVs and that it is reinforced when signaled to others. The altruistic preference is strongest when applies to everybody else, weaker when it reflects a solely personal choice, and weakest when choosing for one’s own child. We conclude that a public choice is considerably more likely to pressure consumers into accepting a more socially beneficial solution. (shrink)

‘Virtue signaling’ is the practice of using moral talk in order to enhance one’s moral reputation. Many find this kind of behavior irritating. However, some philosophers have gone further, arguing that virtue signaling actively undermines the proper functioning of public moral discourse and impedes moral progress. Against this view, I argue that widespread virtue signaling is not a social ill, and that it can actually serve as an invaluable instrument for moral change, especially in cases where moral (...) argument alone does not suffice. Specifically, virtue signaling can change the broader public’s social expectations, which can in turn motivate the adoption of new, positive social norms. I also argue that the reputation-seeking motives underlying virtue signaling impose important constraints on virtue signalers’ behavior, which serve to keep the worst excesses of virtue signaling in check. (shrink)

When you type the word “serendipity” in a word-processor application such as Microsoft Word, the autocorrection engine suggests you choose other words like “luck” or “fate”. This correcting act turns out to be incorrect. However, it points to the reality that serendipity is not a familiar English word and can be misunderstood easily. Serendipity is a very much scientific concept as it has been found useful in numerous scientific discoveries, pharmaceutical innovations, and numerous humankind’s technical and technological advances. Therefore, there (...) have been many books written around the concept. So why do we need this additional book? This is not just another book about serendipity. It has evolved from the Editor’s question lingering for a decade after finishing his widely cited article (coauthored with Prof. Nancy K. Napier of Boise State University, ID, USA) “Serendipity as a strategic advantage?” in T. Wilkinson’s edited volume Strategic Management in the 21st Century, published by Praeger. The Editor and contributing authors have tried to achieve the following in this title. Demystifying the Serendipity Myth The phenomenon of serendipity has always been thought of as a “miracle”. It is the mystery of human innovation and one of the ultimate secrets of our society. But serendipity is not just a lucky coincidence nor any hidden conspiracy. This book explores the science of the information process behind this seemingly miraculous phenomenon. It connects human society with nature, going back to the root of our existence and looking at the flame of survival to discover the harmony in making creativity. Presenting the nuts and bolts of being an adventurer of science The authors present their conceptual investigations into serendipity’s nature and its mechanism by examining interesting real events and stories. The content is thought-provoking, and readers are led to question and explore their own life stories and problems along the journey of reading this book. Catching an elusive high-value target requires great strategies and efforts. But there are no dark secrets here because this is the “way of nature” – how we humans have always strived for innovation without realizing the blueprints behind such processes. Unlike other books on serendipity, this book will show you that a powerful “secret” is closer than you think. Delivering practical uses for different audiences By understanding the conditionality and survival drivers of serendipity, individuals or organizations can make better decisions on creating the right environment to facilitate the encounter and attainment of this valuable phenomenon. For scientists: With clear explanations of the information processes underlying serendipity, flexible theoretical frameworks of mindsponge and the 3D principle of creativity, researchers are provided with the tools they need to dig deeper into their own fields of study and find practical applications, be it psychology, economics, sociology, or anything that involves innovation (which is, in fact, every scientific discipline). For curious casual readers: Everybody needs innovation to make breakthroughs or spice up one’s life. If you think great ideas come to people randomly from an unknown fairy place, this book will convince you otherwise without taking away that awe and wonder. But above all, you will know how to become more creative, scientifically and straightforwardly, with no snake oil and no weird tricks. For ambitious business people: The flame that brought about great successes throughout human history is within you. But you can only use it if you understand it. While others wait for serendipity to come, you will be able to actively hunt for those precious moments. As it has always been: the best hunters triumph, not the passive wanderers. And in this age of information chaos, finding the golden fruits is not easy. Those from information technology know this problem well, and this book is the treasure map that they have been seeking to navigate that stormy ocean looking for jewels. Like a kingfisher tracking its prey through the water, waiting to gracefully strike, with serendipity, a person seizes the prize of creativity amid the chaos of life. ¤ ¤ ¤ Official introduction: The book explores the nature, underlying causes, and the information processing mechanism of serendipity. It proposes that natural or social survival demands drive serendipity, and serendipity is conditional on the environment and the mindset, on both individual and collective levels. From Darwin's evolution theory to Sun Tzu's war tactics, major innovations throughout human history are unified by this key concept. In the rapidly changing world, information is abundant but rather chaotic. The adaptive power of serendipity allows people to notice treasures within this wild sea, but only for those who understand how it works. To increase the probability of encountering and attaining serendipity, one should employ the mindsponge mechanism and the 3D process of creativity, for without these frameworks, serendipity is truly an elusive target. The book also discusses methods to build environments and cultures rich in navigational and useful information to maximize the chance of finding and capitalizing on serendipity. As a skill, serendipity has a resemblance to how kingfishers observe and hunt their prey. (shrink)

The paper investigates what type of motivation can be given for adopting a knowledge-based decision theory. KBDT seems to have several advantages over competing theories of rationality. It is commonly argued that this theory would naturally fit with the intuitive idea that being rational is doing what we take to be best given what we know, an idea often supported by appeal to ordinary folk appraisals. Moreover, KBDT seems to strike a perfect balance between the problematic extremes of (...) subjectivist and objectivist decision theory. We argue that these alleged advantages do not stand up to a closer scrutiny: KBDT inherits the same kinds of problems as alternative decision theoretic frameworks but doesn’t retain any of the respective advantages. Moreover, differently from other knowledge-action principles advanced in the literature, KBDT cannot fully explain the intuitive connections between knowledge and rational action. We conclude that the most serious challenge for knowledge-based decision theorists is to provide a substantive rationale for the adoption of such a view. (shrink)

Most elpistologists now agree that hope for a specific outcome involves more than just desire plus the presupposition that the outcome is possible. This paper argues that the additional element of hope is a disposition to focus on the desired outcome in a certain way. I first survey the debate about the nature of hope in the recent literature, offer objections to some important competing accounts, and describe and defend the view that hope involves a kind of focus or attention. (...) I then suggest that this account makes sense of the intuitive thought that there are moral and pragmatic norms on hope that go beyond the norms on desires and modal presuppositions. I conclude by considering some key questions. (shrink)

Virtue signaling—using public moral discourse to enhance one’s moral reputation—is a familiar concept. But, what about profile pictures framed by “Vaccines work!”? Or memes posted to anti-vaccine groups echoing the group’s view that “Only sheep believe Big Pharma!”? These actions don’t express moral views—both claims are empirical (if imprecise). Nevertheless, they serve a similar purpose: to influence the judgments of their audience. But, where rainbow profiles guide their audience to view the agent as morally good, these acts guide their (...) audience to view the agent as epistemically good. They are instances of epistemic virtue signaling. The first goal of this paper is to offer an account of epistemic virtue signaling. I argue that epistemic virtue signaling occurs through both behavioral and propositional signals, and serves purposes similar to those of moral virtue signaling across a wide variety of discourses. The second is to show that there is much work for this concept to do. In particular, this concept illuminates a double bind faced by those who suffer from and seek to overcome testimonial injustice. I close by demonstrating how this double bind arises in the dissolution of medical autonomy, focusing on the care gap faced by pregnant women of color in the United States today, as compared with their white counterparts. (shrink)

Nietzsche is not known for his theory of empathy. A quick skimming of the Stanford Encyclopedia of Philosophy entry on empathy demonstrates this. Arthur Schopenhauer, Robert Vischer, and Theodor Lipps are among those whose views are considered representative, but Nietzsche has been simply forgotten in discussion of empathy. Nietzsche’s theory of empathy has not yet aroused sufficient interest among commentators. I believe that his views on this subject merit careful consideration. Nietzsche scholars have been interested in his naturalistic (...) accounts of other phenomena, but there seems to be relatively limited interest in his naturalistic account of a phenomenon that is so central to his disagreement with Schopenhauer, namely, empathic concern for others. This is surprising because Nietzsche makes a valuable contribution; he has views more in keeping with contemporary theories of empathy than others of his time. My goal here is to fill in this gap in the scholarship and provide the first thorough analysis of Nietzsche’s theory of empathy, which appears most clearly in Dawn. (shrink)

I present and defend the generalized selected effects theory (GSE) of function. According to GSE, the function of a trait consists in the activity that contributed to its bearer’s differential reproduction, or differential retention, within a population. Unlike the traditional selected effects (SE) theory, it does not require that the functional trait helped its bearer reproduce; differential retention is enough. Although the core theory has been presented previously, I go significantly beyond those presentations by providing a new (...) argument for GSE and defending it from a recent objection. I also sketch its implications for teleosemantics and philosophy of medicine. (shrink)