Open Journal of Philosophy 2012. Vol.2, No.4, 235-243 Published Online November 2012 in SciRes (http://www.SciRP.org/journal/ojpp) http://dx.doi.org/10.4236/ojpp.2012.24035 Copyright © 2012 SciRes. 235 The Structure of Explanations and Counter-Explanations of Homosexuality Fabrizzio Mc Manus Laboratory of Social Studies of Science, Faculty of Sciences, Universidad Nacional Autónoma de México, Mexico City, Mexico Email: FabrizzioMc@yahoo.com Received July 27th, 2012; revised A ugust 28th, 2012; accepted Septem b er 1 2th, 2012 The aim of this paper is to revisit an ongoing controversy within the so called “Science Wars”; more spe- cifically, I will address a particular topic within the “human nature” debate: the ontological and episte- mological status of homosexuality. I claim that, in this particular chapter of the “Science Wars”, we are continually left in an explanatory impasse even when more data are collected, more rigorous experimental techniques are developed, more subtle arguments are offered and more pluralistic narratives are told. My diagnosis of the source of this impasse leads me to the conclusion that here we are dealing with a struc- tural problem that cannot be solved with an elaboration of new models and theories that maintain an on- tology and an epistemology that are no longer suited as an explanans of human nature in general, and homosexuality in particular. Nevertheless, my analysis of the structural features of the biological explana- tions and the constructivist counter-explanations also leads me to the belief that, although biologists do not fully understand the intricacies of subjects, neither constructivists understand the facticity of evolution and the challenge that it implies. If so, then the subject might be the right target of explanation. And, if so, constructivists might be right about the uniqueness of human homosexuality as a modern, western phe- nomenon explainable in terms of subjectivities and identities that mold and are molded by desires and in- stitutions. But, if they are, evolution is not expendable because now we are facing a most intriguing ques- tion: How is that we humans became subjects? Keywords: Homosexuality; Human Nature; Philosophy of the Subject Introduction The aim of this paper is to revisit an ongoing controversy within the so called “Science Wars”; more specifically, I will address a particular topic within the “human nature” debate: the ontological and epistemological status of homosexuality—or, should I say human homosexuality? On the one hand, biologists, psychologists and physicians have attempted to explain homosexuality as a biological phe- nomenon caused by biological forces. These biological forces are sometimes catalogued in terms of proximate and ultimate causes, following in this Mayr’s classical dichotomy (Mayr, 1993); proximate causes can also be subdivided in terms of internal vs external forces, although this second dichotomy is problematic and s e l d o m used . Proximate (internal) causes are usually bio-molecular mecha- nisms or develop menta l path ways pr esent in specif ic individu als (Hamer et al., 1993; Hamer, 1995; Hu et al., 1995; LeV ay, 1991; LeVay & Hamer, 1994; Pillard, 1997; Rahman & Wilson, 2003; Savic et al., 2005; Savic et al., 2008; Swaab et al., 2001; Yama- moto et al., 1996); proximate (external) causes are usually en- vironmental phenomena, such as pollutants or maternal effects, that act as developmental insults capable of disrupting canalized developmental pathways that in “normal” circumstances pro- duce a “normal” trait: an heterosexual sexual orientation (see chapter 6 at Poiani, 2010). Ultimate causes are, in contrast, evo- lutionary forces such as sexual selection, group selection, kin selection or even genetic drift, all of these acting on populations (Hutchinson, 1959; Kirby, 2003; Muscarella et al., 2001). But not all biological explanations of homosexuality are al- ways so dichotomic. In the last twenty years different approxi- mations to biology in general, and to evolution in particular, have produced explanations that not only criticize the very dichotomy of proximate vs ultimate causes—I have in mind approaches such as Developmental Systems Theory (DST) (Griffiths & Gray, 1994; Oyama et al., 2001) and Evolutionary Developmental Bio logy (Evo-Devo)-, bu t also the idea that there are species-specific mechanisms responsible for making an individual homosexual. The works of Joan Roughgarden and Aldo Poiani, alth ough very d ifferent i n their d etails, point to new explanations that de-essentialize homosexuality as a biological explanandum by conceiving it as a multiply realizable phe- nomenon. This leads to new and interesting scenarios in which cooperation and agency (Roughgarden, 2004, 2009) and be- havioral and neuronal plasticity (Poiani, 2010) become more important elements for any biological explanation of homo- sexuality. On the other hand, philoso phers, sociologists, anthropologists and literary critics have resisted these explanations and have advanced a col lection of what I call counter-explanations (Byne, 1994; DeLamater & Hyde, 1998; Fausto-Sterling, 2000; Roof, 1992; Rosario, 1997). Counter-explanations are not alternative explanations although there is a myriad of alternative explana- tions emanating from these disciplines. Instances of alternative explanations are: 1) the family of constructivist approaches that encompass psychoanalytical and
F. MC MANUS psychodynamic explanations (e.g. Dean & Lane, 2001); 2) the sociological models that focus on social roles an d thick and thin descriptions of actions and signified traits that constitute gender (Dickinson et al., 2003; Prieur, 2008); 3) or, even, the Queer Theory approach centered upon performative speech acts, prac- tices of embodiment and intercorporeality, and the interaction between agency and structure in the conformation of modern subjectiviti es in term s of identit ies (Butler, 1993; Sullivan, 2003 ; Weiss, 1999). But these are NOT counter-explanations although they might contain elements of them. Let me elaborate, th en, this distinct ion a little further. B iological explan ations hav e produced a universe of data that in principle are evidence in favor of the biological nature of homosexuality. These data cannot simply be ignored, they have to be counter-explained and that is exactly what counter-explanations do: they explain away these data. In a sense alternative constructivist explanations r equire coun- ter-explanations for two different reasons. First, counter-ex- planations question the objectivity and validity of the data- driven biology by means of a dialectic deconstruction of the subject-object relationship that seeks to show how cultural bi- ases are projected upon these data. Second, this dialectic decon- struction also questions an implicit axiom regarding causation that informs all biologic al exp lanations; this axiom usually tak es the form of an implicit commitment towards an ontology of homosexuality in which homosexual subjects possess homo- sexual bodies that are a type of causally structured body. I will elaborate on the details of this axiom later but I would like to point out that by bringing this axiom into question it is possible to problematize the very notion of causation that un- derpins biological explanations and, hence, to offer alternative explanations that emphasize subjectivity, identity, psychody- namics and cultural contexts as more relevant elements for any account that attempts to understand homosexuality. Nevertheless, counter-explanations and alternative explana- tions run the risk of dematerializing the homosexual subject or, at least, to conceive his or her materiality only in terms of sig- nified bodies nested within networks of practices, actions and meanings. The risk of course is not only theoretical but also ethical and po litical. This i s so becaus e resisting bi ological deter- minism, essentialism or some mild forms of evolutionary ide- ologies (Marks, 2012) should not take us into an allegiance with creationism or intelligent design. We are, after all, evolved be- ings and that is a fact that matters. And this fact m atters because if, at the end of tim es, a Peircean community of scientists decides that constructivist alternative explanations are right, a fundamental question is going to arise: How an evolved animal became capable of being a subject? A subject capable of performing speech acts, endorsing identities, possessing an agency, being molded by a structure, etc. Surprisingly this question takes us to an old branch of phi- losophy and a very new branch of biology. As Fernando Vidal (2006) has shown Anthropology used to be understood, at least in the XVIII century, as the branch of metaphysics that deals with the problem of what is to be a human. But now some evo- lutionary biologists have begun to think about the evolved cog- nitive and emotional complexity of human beings. A few have even suggested the necessity of a new approach which has been labeled as “Evolutionary Social Constructiv ism” (Wi lson, 2005) . Poiani’s explanations go some steps further in the right direction, if I might say so, but they are still prone of counter-explanations. And this should raise a n eyebrow for philosophers of science. What is going on in this par ticular chap ter of the “ Science Wars” that continually leaves us in an explanatory impasse even when more data are collected, more rigorous experimental techniques are developed, more subtle arguments are offered and more pluralistic narratives are told. Why biology is still seen by con- structivists as a form of es sentiali sm eve n aft er bi olog y itself has fought hard in order to overcome an essentialism of species (Hull, 1965) and traits (Rieppel, 2005) and has even reinvented itself as DST and Evo-Devo exemplify. Why constructivist themselves fail to see this fact that matters: an evolved animal that became a subject. And why constructivism is still seen by many biologists as mumbo-jumbo jargon incapable of explain- ing anything. My hypothesis, and the main objective of this paper, is to advance as an answer the possibility that we are dealing here with a problem that lies outside the data, the techniques and the particular arguments and lies in the very structure of the expla- nations and counter-explanations offered so far. Maybe the pro- blem is structural and cannot be solved with an elaboration of new models and theories that maintain an ontology and an epis- temology that are no longer suited as an explanans or counter- explanans of human nature in general, and homosexuality in particular. In order to el abo rat e such an ar gu ment this p aper is divide d in four sections. The first section tackles with some structural elements present in most biological explanations of homosexu- ality. The second section, on the other hand, analyzes structural elements of the counter-explanations. The third section is dedi- cated to the problem of the evolved subject and should be un- derstood as an attempt to bridge this explanatory impasse or, at least, to show why it eventually must be bridged. Finally, the fourth section presents the conclusions of this paper. Structural Elements of Biological Explanations Maybe two of the most famous biological explanation of homosexuality nowadays are, first, the infamous and hypothe- sized gene on the q28 section of the X chromo some (Hamer et al., 1993) and, second, the equally famous and assumed dimorphism in the third Interstitial Nuclei of the Anterior Hypothalamus (INAH3) (LeVay, 1991). But biological explanations are much older than genetics and neurosciences and we could argue that they actually date back to the XIX century and, even when they are stated in terms of the modern theory of evolution (the so called New Synthesis), they date back to the late 1950s (Hut- chinson, 1959). So, this background indicates that our domain of interest en- compasses 150 years in which biology has experienced funda- mental changes m ore than once. At first sigh t this might t akes us into the beli ef th at ver y few element s, if an y, can be identified as conserved structural features constitutive of these explanations. In this section I will show that, these changes notwithstanding, there are such elements. The first element that I would like to consider as a conserved structural feature has to do with the most basic strategy for classifying living beings in biology, at least since the XVIII century: seeking for homologies (or affinities, as they used to be called prior to th e mid-XIX centu ry). There are m any definitions of homology and some actually pre-date D arwinis m but the core of the concept has to do—now—with a similarity among organ- isms of the same or different species caused and explained by common descent. Copyright © 2012 SciRes. 236
F. MC MANUS Examples of this way of thinking about homosexuality abound. For example, Bruce Bagemihl (1999) has compiled an entire book of cases o f non human homosexuality, transexuality, intersexualit y and trasvesti sm. Yamamoto and co-work ers (1996) have tried to use Drosophila as a model organism for finding the specifics of the bio-molecular mechanism that produces homo- sexual behaviors not only in flies but maybe also in humans; Frank Beach (see Fausto-Sterling, 2000) used a very similar approach with mice ca. 1940s although under a less mechanistic view of behavior . Even Roughgar den and Poiani s eem to assume that homosexuality in humans is, in a sense, an instance of the same kind of exp lanandum as homosexuality in d ifferent species of birds and mammals. But these authors are not alone. Evolutionary explanations also assume that homosexuality in humans is an instance of a type of phenomena that encompasses several taxa and so should be explained i n simil ar terms acro ss all of th em, no twithstanding if these terms invoke kin selection, group selection or other evolutionary forces. And historically speaking XIX century biology was not very different (see Rosario, 1997 and the rest of the papers in the book). Most sexologists invoked pseudo-Haeckelian explana- tions of homosexuality that involved phylogenetic atavisms or degenerations th at led into more primitive behavio rs; hence, they assumed that homosexuality was comparable to other animal behaviors. Legal medicine, even in the XX century, still con- tinued to use that framework as can be shown with the para- digmatic case of the spanish endocrinologist Gregorio Marañon (1960; see also Ferla, 2004). What is common to all of these explanations is what I have previously named “an empiricism regarding sex and gender categories” (Mc Manus, 2010, in press) that basically implies a commitment towards a westernized and modern view of sexu- ality in which variables such as 1) sex; 2) gender; 3) sexual orientation—understood in terms of the gender of the intended object of desire; 4) stereotyped physical appearances and 5) stereotyped behaviors are considered sufficient to describe all forms of what we, in the West , call “s exuality”; at the sam e time, it implies a rejection of the relevance that the phenomenological dimensions in which these categories are actually lived and experienced by human beings might possess. This implies a co mmitment towards the universality—cultur al as well as interspecific—of these variables not only in terms of their mutual independence but also in terms of their capacity to generate a theoretical multi-space in which every animal sexual behavior can be mapped—as the book of Bagemihl perfectly illustrates. In other words, what these explanations have in common is the idea that sexuality corresponds to a family of traits in which sexual orientation can be conceived as a particular trait ho- mologous among different animals and with different character states that correspond to what we in the West call “homosexu- ality”, “heterosexuality” and “bisexuality” (this corresponds to what I hav e la beled as models o f taxonomic identity [Mc Manus, 2009]). These similarities, as all homologies, could then be under- stood as structural similarities in the organization of the arche- types of organisms (Baupläne) and so similarities due to com- mon descent. This will make homosexuality a trait comparable with classical instances of homologies such as the arms of hu- mans and apes, the wings of insects and the gills of crustaceans, the seeds of coniferous and flowering plants, etc. Nevertheless, the concept of homology is not an easy one to grasp. This is so because the conc ept of the archet ype flourishe d in the german tradition of biology and, as it is well known, this tradition was deeply influenced by Kant. But already in the XIX century biologists abandoned a strictly kantian epistemology re-tooling in the way the very concept of homology. I will sidestep the many intr icacies of th e concept as well as its history but I would like to point out that archetypes are not entirely dead in biology. The discovery of the Hox genes in a sense revitali zed the idea that there is a sort of archetype codifi ed in the genome. More recently, Evo-Devo has attempted to ex- pand this notion by talking about developmental pathways and phylotypic stages causally responsible of producing form (Striedter, 2004). Anyway, the idea of behavioral homologies has its own his- tory (Hebb, 1953; Rendall & Di Fiore, 2007) and it is quite a history. On the one hand, the very possibility of talking about behavioral homologies has been disputed because, for many scholars, behavior is tantamount to a functional dimension and so not prone to a structural analysis; on the other hand, for those who accept the possibility of behavioral homologies, it is still a matter of controversy if behavioral homologies could exist even when there are no structural underlying homologies. Again, I will sidestep these philosophical discussions and I will focus on the relevant consequences for our own topic. The relevant aspect, conserved across 150 years of biology, has to do with the possibility of conceiving sexuality as a family of traits, in general, and sexual orientation, in particular, as a type of trait with many instances such as homosexuality, bi- sexuality and heterosexuality. The feasibility of hypothesizing that homosexuality might be an instance of a homologous be- havioral trait helps us to understand several things. First, why we try to use the very same theory to explain homosexuality in humans and other animals. Second, why we seek for similar mechanisms underlying homosexuality across different species. Third, why many biologists that accept homosexuality as a multiply realized trait still consider it the same phenomenon even when it is generated by different causal mechanisms (if, of course, you accept that behavi oral homologies can occur without an underlying morphological homology). Fourth, why the work of anthropologists is so easily discarded when they insist in showing the cultural differences regarding “sexuality”; this has to do, I might say in order to clarify the point, with the capacity of the concept o f homology to make “the same” things that might appear very “different”. And this structural feature is by no means privative of the topic here revisited—explanations of homosexuality—as can be seen in the work of Paul Griffiths (2011) when he claims that human nature is variable but all v ariations can b e accommodated within the framework of homology. This, in a sense, prohibits any new and cultura lly speci fic traits because all variat ion would be an instance of a rather general kind. If we follow this argument the very concept of homology might allow biologists to conclude that no human behavior is truly unique be cause, even if it does not possess an homologue, it can at least be thought of as a field homologue of a family of behaviors that were precursors of our more complex and signi- fied behaviors—i.e. not homologous to a particular behavior in non human animals but related to them because this human behavior developed by modifying and enriching these behav- iors (Striedter, 2004). The second structural feature I would like to char acterize i s an Copyright © 2012 SciRes. 237
F. MC MANUS elaboration of what Joseph Rouse (1994, 2002) has identified as a form of pernicious philosophical naturalism quite common in cognitive science. He has labeled it as the problem of “the manifest necessity”. This problem is an heir of Wittgenstein’s argument of following a rule (Rouse, 2002). However, this particular v ersion of the problem ar ises when cognit ive scientists (as third person knowers) seek to analyze norms, actions and meanings in terms of natural regularities or causes. In other words, whenever scientists try to ground normativity in causa- tion -understood as a natural necessity. Rouse claims, echoing Wittgenstein, that any analysis of nor- mative phenomena—such as norms, rules, meanings or actions- designed under these lines will fail to explain these phenomena in terms of n atural regularit ies. This is so because the sci entist, as a third person kn ower, faces a finite amount of d ata—thus, his or her interpretations are epistemically underdetermined by evi- dence—and, so, is unable to discriminate among a myriad of possible causal mechanisms capable of producing these data. For Rouse the only possible solution would be to assume that regularities manifest themselves—phenomenologically speak- ing—in such a way that the specific causal mechanism respon- sible for the observed regularities is transparent to the scientist as a third person knower. In other words, if we take causation to be a natural necessary regularity and if we attempt to analyze normative phenomena in terms of causation (both big if’s), then the only way to overcome the underdetermination problem is to suppose that causation manifests itself in such a way that the third person knower correctly identifies the relevant causal mechanism responsible for the normatively guided actions that served as observations1. Now, what is the relationship between this argument and the biological explanations of homosexuality? The s econd stru ctural element is sim ilar to th e previo us argume nt in two respects. Fir st, usually the scientist, as a third person knower, tries to explicate the homosexuality of a subject as if this were a behavioral trait. But the funny thing is that homosexuality is conceived not only as a behavioral regularity but also as a disposition that norma- tively guides and sanctions the behavior of the subject; more- over, as the Kinsey scale illustrates (Fausto-Sterling, 2000; Mc Manus, 2010), h omosex uality, ev en i f con struct ed a s a b ehavio r, also has phenomenological dimensions like arousal, desire and fantasy. So, the first sim ilarit y lie s in t he fa ct t hat h omosexualit y is described at the same time as a normative phenomenon that possess phenomenological dimensions, on the one hand , and as a disposition responsible for the observed sexual and emotional behavior, on the other. In other words, homosexuality as a nor- mative phenomenon is grounded in causation2. Indeed, this ambivalence in the very ontology of what is ho- mosexuality is fundamental for biological explanations because homophobia tends to preclude homosexual behavior in many cultures and because there are situations in which “situational homosexuality” is observed (e.g. prisons). Nevertheless, neither the lack of homosexual behavior in a subject counts as evidence against the hypothesis that he or she might be homosexual nor the behavior, when observed, verifies that he or she is actually homosexual. This is so because the idea of a silent and dormant dis po s it io n helps to establish the supposed universality and transculturality of homosexuality. If this were a motto, it would be more or less like the following statement: “homosexuals are everywhere but they might not be visible in some cultures”. In opposition, the plasticity of behavior aligns itself with the homology-laden reading that makes “the same” things that are “different” be- cause, if homosexual and heterosexual subjects can act as het- erosexual or homosexual subjects—respectivel y—then b ehavior is plastic enough to be molded by cultural dimensions. Second, “the manifest necessity” problem has also a related sibling in this fie ld. We can see th is when we ana lyz e the w a y in which biological explanations of homosexuality connect causa- tion with normativity. In Rouse’s example the problem of the manifest nece ssity was a problem for the researcher because he or she did not have a direct access to the phenomenology of the norms and any attempt to characterize the norms in herme- neutical terms would imply a rejection of the very spirit of naturalism. But biological explanations of homosexuality usu- ally employ subjects that manifest their sexual orientation to the researcher and so the previous problem is bypassed. This allows the identification of a possible causal mechanism that can be taken as the discovery of the natural necessity that manifests itself with transparency into the consciousness of the homo- sexual subject. Let us illustrate this with an exampl e. Simon LeVa y and Dean Hamer (1994) combined their findings in order to offer a more robust causal narrative capable of explaining how genetic dif- ferences could produce a homosexual behavior. They basically endorsed the hypothesis that the genes in Xq28 might be re- sponsible for the morphology of INAH3 and—through an argu- ment mediated by homology which invoked the regulatory dimensions of INAH3 in the sexual behavior of mice—they claimed that this almost insignificant brain modification would produce a feminized behavior in males and, thus, it would make them homosexuals. Of course, these men would not be aware of the underlying morphology—the causative part of the story— but nonetheless it would modify their behavior by structuring in a feminized way their patterns of desire, arousal and sexual fan- tasy and so, eventually, their behavior. Hence, causation mani- fest itself transparently into the consciousness of the first person and so grounds a normative disposition. 1Wittgenstein’s and Rouse’s arguments are much more complex but I will sidestep a full exposition of them because this will not contribute to the general argument of the paper. If interested, the reader should review the problems associated to reglism and regularism as strategies that attempt to characterize norms in terms of regularities and how they lead to an infinite regress (I recommend reading the paper of King Dávalos, 2008, and some other contributions collected at Esteban & Martínez , 2008). 2The idea that sex-generic categories, including sexual orientation, are nor- mative has long been defended in Gender Studies and Gay and Lesbian Studies, at least since Foucault (1977). The phenomenology of these catego- ries is usually taken as evidence of the normative dimensions of them be- cause desire, arousal and fantasy not only guide behavior but also sanction ehavior as enjoyable and pleasurable or disgusting and repelling. When understood as identities their normative dimensions are even stronger be- cause the relation of belonging to a group impose a serious burden upon the sub ect. At this point we could be tempted to conflate this problem with an impoverished view of causation. But we should not go that far. It is true that the previous example seems to accept without a question a bottom-up approach of how diffe r e nt levels of organization present in biological beings causally interact. However, a bottom-up approach to causation does not exhaust all biological understandings of biological causation, certainly not in evolution, development or molecular biology (Craver, 2007; Martinez & Moya, 2011). More complex causal stories can be offered, as can be seen in the proposals of Roughgarden and Poiani. In the case of Roughgarden (2004), social interac- tions among different animals of the same sp ecies might pr oduce Copyright © 2012 SciRes. 238
F. MC MANUS alterations in behavior that have also morphological and phy- siological correlates. In the case of Poiani, the interactions among different levels of organization can also produce altera- tions in behavior. But a more complex causal narrative is not tantamount to a rejection of a pernicious naturalism. All of these models still assume that th e phen omenologica l dimensions of homosexuality in humans ar e cau sally produ ced b y underl ying m echan isms and so that homosexuality in humans, even if richer because of its meaningfulness, is still a hom ologue of homosex ual behaviors in non human animals. All of these models still assume that these causal mechanisms will manifest themselves with transparency in the consciousness of the subject, making him or her homo- sexual. Of course, the problem of underdetermination is still present because there is a m yriad of bio logica l mech anism s that could in principle produce that behavior but, at least, the problem of bridging causation and normativity seems to be solved. Also avoided is the problem of an infinite regress present in the original Wittgensteinian argument. Curiously, this second structural element can be restated as a commitment to an ontological view on the causes of homo- sexuality in wh ich homosexual subj ects have homosexual bodies, i.e. their bodies are causally structured in a different form than heterosexual bodies. This does not imply a tension neither with the multiply realized view because these causal mechanisms might be different in different species or even organisms, nor implies a tension with the first structural element because, as I said before, behaviors can be homologues even if their under- lying developmental pathways are not (a phenomenon known as developmental drift). And even if these behaviors were not homologues, they could still be thought of in terms of evolution if they happen to be similar solutions to similar problems: i.e. analogues. However, I will go further in this analysis in order to claim that the first and second conserved elements actually act syner- gistically. This is so because, if homosexuality, understood as a normative phenomenon, for example, as an identity or subjec- tivity, can be grounded in causation, then, the existence of similar dispositions in non human species (similar up to a point, of course, because these disposition would most likely not pos- sess the phenomenological correlates that they have in humans) might indicate the existence of similar mechanisms in those species an d , so, w ould all ow u s to th in k it i n te rm s of h omol og y. And the synergy goes both ways because, if we assume that sexual orientation is a trait present in human animals and non human animals, then we, per force, would seek for explanations that do not invoke elements only present in humans, elements such as language, meaningful actions, subjectivities, etc. Structural Elements of Counter-Explanations For many biolog ists the accus ations of es sentialis m are, to sa y the less, puzzling. For them, constructivists cannot seriously believe that modern evolutionary biology resembles classical Aristotelian or Platonic doctrines of essences. Moreover, mod- ern biology emphasizes variation and demographic thinking, boundless and endless changes in morphology, physiology and behavior—even if we accept t h a t not every point in the morpho- space can be occupied by living beings. Evolutionary theory implies that organisms co-evolved with their environments and, so, that they lack intrinsic properties because everything—adaptation or constraint—they exhibit is a relational property; every trait is th e result of previous cycles of change with modification in an environmen t al context. But in light of the elements described in the first section of th is paper we can understand wh y constructivists accuse biologi sts of essentialism. The idea that, notwithstanding how much change we detect, a behavior is still the same behavior, in the sense of being a homologous behavior (or an analogous behavior and so the same solutio n to a similar si tuation), and tha t it is the r esult of a causal mechanism that manifest itself in the consciousness of human subjects, resembles essentialism enough in its trans- historicity to justify the label. But it does not resemble essen- tialism enough to be equated with fixism or univocal realizabil- ity. And this last point is fundamental because classical essen- tialisms will not admit the identity of essences when there is a serious possibil ity of endl ess and bou ndless variati on, on the o ne hand, and a multiplicity of causal pathways capable of producing the same phenomenon, on the other hand. I believe this helps to explain, at least partially, why we are stuck in an explanatory impasse. Biologists fought against es- sentialism understanding it as species (and traits) fixism and univocal realizability. Constructivists went a step further and fought against the trans-historicity implicit in the homologation of different culturally-laden phenomena that were interpreted as the same. But this last point is only one of the structural features of counter-explanatio ns. There are at least two more elements that I advanced in the introduction of this paper. Both emerge from a dialectic decon struction of th e subject-objec t relationship b ut, on the one hand, one horn of the criticism refers to the limits of objectivity while, on the other han d, the second hor n refers to t he implicit axiom of a causally structured homosexual body. At this point it might be important to clarify one thing before getting started. I am the one who reads most counter-explana- tions as offering a dialectic deconstruction of the subject-object relationship; the authors I will revisit did not necessarily employ this terminology. Nonetheless, the idea of framing the counter- explanations in these terms occurred to me when I read some criticisms exposed by Donna Haraway (1989) against the pri- matological research on the supposed heritable nature of intel- ligence; what I saw in her crit icism was a general feature of s ome counter-expla nations regarding h u man nature. With this in mind I will proceed by examining a couple of examples. Example No. 1: When Simon LeVay claimed that he had found a dimorphism in the hypothalamus of men Judith Roof (1992) counter-explained his findings by arguing that he was projecting onto the data the very dynamics of exclusion and in- visibility that were definitory of the political vulnerability of lesbians (and, I will add, other subaltern sexualities). According to Roof, lesbians were discriminated by men because they were women and they were also discriminated by heterosexuals be- cause they were homosexuals but, worse, they were discrimi- nated by gay men because the latter still exerted a privileged male-centered view that subordinates and excludes women, including lesbians. So, Roof interpreted LeVay’s explanation as an erasure of lesbianism as an expla nandum because LeVay’s model was only capable of explaining male homosexuality and was, as a result, incomplete. Moreover, L eVay’s nat uralization of homosexuality redeemed gay men but not lesbians as a part of nature; and, as Roughgarden once said, the right to feel as a part of nature, as belonging to the natural order, has important psychological Copyright © 2012 SciRes. 239
F. MC MANUS effects on the Self (2004). Male homosexuals in the work of LeVay were the result of a naturall y occurring causal m echanism and, so, could not be conceived as morally vicious but the same could not be said about lesbians. Roof offered other arguments against LeVay’s hypothes i s but the previous one is interesting for the following reason. It ac- cuses a researcher of inadvertently projecting his cultural biases onto the data in order to use those data to validate his own privileged position as a subject, in this case, as a gay man. Example No. 2: INAH3 is not the only brain region that has been hypothesized as causally responsible for the generation of homosexual beh aviors i n humans . The Corpus Callosum (CC) is another famous brain structure that has been considered a pos- sible candid ate f or causing behav iors such as homosexuality and gender identity diso rders. Indeed, this explan ation was criticized by Anne Fausto-Sterling (2000) in her book Sexing the Body. Fausto-Sterling offered an elabor ate argum entation a gainst the se data by showing how the Corpus Callosum was, at the same time, a mathematical, material and literary object. For her, it was important t o show that the CC was materia l and mathematical because both are aspects of scientific objectivity. Much has been written in philosophy of science about objectiv- ity (Daston & Galison, 2010; Kuhn, 1977; Longino, 2002) but now it is more or less widely recognized that this concept en- compasses several aspects. For example, there is the procedural side of objectivity connected with the standardized techniques and mathematical tools that allow us to model natural phenom- ena by abstracting and extracting them away from their original contexts of occurrence in order to produce what Latour (1992) calls immutabl e and combinable mobiles. These mobiles are an instance of a circling reference (Latour, 1999) that functions as evidence in support of some particular hypothesis by establishing their accuracy and, so, they exemplify a different aspect of objectivity: representing nature. But th ey are also associated with a third aspect of objectivity that grounds an interpretation of objectivity as inter-subjectivity: the replicabil- ity of observations. These mobiles result from standardized procedures that in principle warrant the cancellation of idiosyn- cratic biases by ensuring that any subject might be able to re- produce those results. In my view Fausto-Sterling concentrated so much in these elements because it is a disservice to criticism to ignore the methodological intricacies of science as well as its sociological complexities; t o ac cu se scientists of projecting their biases upon data without even analyzing their methodologies and the socio- logical processes of mutual validation is not only risky but also is the best way to generate a co n u ndrum in which both sides of the dispute end up with a philosophical deafness hard to overcome. Nevertheless, Fausto-Sterling understood something that some philosopher s of sci ence h ave found ha rd to assi milate. The task of philosophy should not be to serve as an unconditional defender of science but, on the contrary, to criticize it when it claims more than it can prove. The other side of her argument showed that the CC was a literary object because the causal narrative offered by physicians, biologists and psychologists is still a narrative that situates within a background the empirical findings and connects them in order to articulate an integrative explanation of the phenomenon in question. In a sense, Fausto-Sterling engaged in an informed criticism that situated the scope of these results by emphasizing the com- plex materiality of the CC. On the one hand, the materiality of the CC is the m ateri alit y of the bo dy and so it is c onnecte d to th e causal arrangements that underlie behavior . On the oth er hand, i t is the materiality of evidence; but a piece of evidence is not tantamount to a piece of the body because the evidence is pro- duced through a set of standardized techniques and procedures that translate a tridimensional living body into bidimensional sections of a corpse or, more correctly, that translate bidimen- sional sections of a corpse into the inferred structure of a tridi- mensional living body. And this process of integrating different sets of evidence and interpreting them is still prone to cultural and systemic biases and, in some cases as Fausto-Sterling showed, to blatant meth- odological err ors. In the particular case of the CC, distinguishing between the typically male and the typically female morphs of the CC was controversial not only because there was no stan- dardized technique for doing it but also because it was done without specifying clear cut criteria that guided the construction of this taxonomy. Claiming that sexual orientation or gender identity resulted from the prese nce of a typically femal e morph in males or a typically male morph in females was dubious because the underlying classification was dubious. If this hy- pothesis was accepted, wrote Fausto-Sterling, was not because of the merits of the research but because it confirmed a cultural and systemic bias: gay men and Male to Female Transexuals (MTF) are just femi nized men and le sbians and Fema le to Male Transexuals (FTM) are just manly women. Anyway, both cases exhibit a common structure already an- ticipated in the introduction. In both situations we find a criti- cism that deconstructs the supposed validity and objectivity of the evidence and the causal narrative erected upon it through a dialectic analysis of the relationship between the subject-the scientist and the object-the data. More exactly, in both cases the criticism targets this implicit dialectic that arises as a consequence of the demands of objec- tivity upon the researcher. This is so because objectivity is un- derstood as an ethical and epistemic neutrality in which the values, goals and expectations of the scientist should be can- celled in order to avoid any interference. The standardized tech- niques, the mathematical tools and the replicability and inter- subjective accessibility of the data should grant the veracity of the results. Hence, this produces an inversion of positions in which the scientist tr ansfers to the data his or her own position as a subject. And so, the data are in principle “telling us their truth”; they occupy the s tructu ral pla ce of the subject becaus e they enunciat e what is the case. But this enunciation is only possible because the experimental settings stabilized—through standardized pro- cedures, mathematical models and theoretical interpretations— the possible outcomes of the experiment. In other words, the object as a subject tells its truth in the vocabulary of the subject as an object because the latter transferred not only his or her position but also made possible the capacity of enunciation of the former by generating a context free of interference in which it can tell us its truth in a language we can understand. Moreover, what is the case and what is the truth is the case about some human subjects, is th e t ruth o f s ome h uman su bjects. This makes the subject (the homosexual subject in this instance) the object of enunciation. As structural positions, the subject becomes the enunciated object and the object becomes the enunciating subject. Sadly, at this point homosexuality is naturalized and the procedural dimensions of objectivity that broug ht i nto b eing and kept the stability and immutability of these combinable mobiles Copyright © 2012 SciRes. 240
F. MC MANUS are usually taken as a d ispos able la dder. Th e liter a r y dime nsion s of these mobiles are forgotten and they are reified as causal mechanisms (Winther, 2006, 2009). Statistical correlations are read as causal re lations, sociall y constructed taxonomie s are read as natural kinds and local experimental findings are taken as robust and trans-historical regularities. But this is only half of the story. This is so because humans tend to mold their behaviors and identities according to the available descriptions of themselves—as Hacking (2001) has famously claimed by labeling this process a “looping effect of human kinds”. Th e funny thing about this l ooping effec t is that it might produce, in some but not all cases, a more stereotyped behavior. Thus, the subject reclaims a subjectivity apparently enunciated by the object and, so, the hermeneutical circle fin- ishes with a subject fully convinced of the naturalness of his or her subjectivity. Precisely because of this last point counter-explanations are usually the first element of constructivist alternative explana- tions. They counter-explained the data and restored the com- plexity of the subject and, therefore, advanced the possibility of searching for a different type of explanation. Towards a Truly Evolutionary Social Constructivism But there is this fact that matters: we evolved. We know we are subjects and we also know that bacteria are not subjects, protozoa are not subjects, plants and fungi are not subjects, sponges are not subjects (sponge Bob notwithstanding), worms are not subjects and, about apes and some mammals, well, we are not so sure anymore although for centuries we would have said that they are not subjects. And, by subjects, I mean that we are aware of our own envi- ronment and about ourselves, even of our own awareness of being aware, but I also mean that we are capable of acting ac- cording to goals, desires and norm s . We are s ubj ects be caus e we can be held a ccountable for our actions—we can be ethically and epistemically responsible and, so, we are not merely responsive, but we can also be subjected by institutions created by our in- tentionality, by our capacity to know that the other knows that we know; hey, we can promise! We are subjects because we are capable of acting as a collective because we can share—mainly through language—our goals and means to achieve those goals, but we are also subjects because we can exert power upon others through those i nstitutions; we can le t them k now things that w ill alter their behavior, we can even menace or threaten them (Habermas, 1999; and Schmitt, 2004, elaborate on some of the previous points). This is exactly what allows us to have a world, to have a cul- ture, because, in Heideggerian terms, the subject is a Dasein, it does not possess properties but existentiaries as forms of be- ing-in-the-world (Heidegger, 1927). But, surprisingly, this ap- parent difference might be the reason for taking evolution more seriously, as Der rida advanced in The animal tha t Therefore I am (2008) when he concluded that, even if stones are Weltlos (without a world) and most animals are Weltarme (poor in world), evolution is still fundamental because our capacity to be a Dasein must have evolved from a previous condition of being poor-in-world. Derrida himself criticized philosophers, specifi- cally continental philosophers, for ignoring the fact that we evolved. If so, then the subject m ig ht be the right target o f explanation . Constructivists might be right about the uniqueness of human homosexuality as a modern, western phenomenon explainable in terms of subjectivities and identities that mold and are molded by desires and institutions. But, if they are, evolution is not expendable because now we are facing a most intriguing ques- tion: How is that we humans became “evolutionarily” and be- come “developmentally” subjects? Such a change in the explanandum is not necessarily disrup- tive to the research programs of physicians, psychologists and biologists. After all, as Millikan (1984) has shown in the case of explanations of a daptations, sometim es we misidentify th e target of an explanation and attempt to explicate what results to be a mere consequence of a more interesting and fundamental phe- nomenon. For example, we might try to explicate why the stru- cture of our hands is an adaptation for writing but, if we do this, we have trans-historicized writing and misidentified a more interesting and fundamental phenomenon: the capacity of our hands to handle objects with an incredible precision and eye- hand coordination. Similarly, if homosexuality is explained in constructivist terms, then the more interesting and fundamental phenomenon is our capacity to become subjects. Cognitive scientists, neurophilosophers and biologists have already begun research programs that might be able to tackle some parts of the previous question. Kim Sterelny, for example, is interested in the evolu tion of ag ency, desires a nd intentional ity (2001); according to him intentionality arises in epistemically translucent environment (examples of environments such as these are social environments or highly heterogeneous environ- ments) in which there is no singular robust environmental clue and, so, it is more adaptive to triangulate different and inde- pendent environmental clues in order to know what are the exact environmental conditions and how we might proceed in such scenario. Social environments are an instance of this kind of scenario because a conflict of interests might arise among dif- ferent organisms which may lead to cheating. Desires, on the other hand, evolved in order to help the organism to ponderate which activities should be a priority. Sober and Wilson (1998) is anoth er goo d examp le of th is new trend in biolog y. They ar e intere sted in the evolu tion of socia lity and normativity. Wilson in particular has advanced the above cited “Evolutionary social constructivism” but, sadly, he has framed it in li ght of classical population ge netics (Wilson , 2005). This is unfortunate because he understands plasticity only in terms of norms of reactions, i.e. as the capacity of a genotype to produce different phenotypes in different environments. This seriously restricts the scope of his proposal because it still im- plies a commitment with a view on phenotypic traits in which they are always the expression of an underlying genotype. In that regard, Poiani is probably the biologist that has better understood th e challenges pos ed by constructivists. Although his proposal is prone to counter-explanations because it still tries to explain homosexuality not as a consequence of being subjects but as a homologous trait present in humans and nonhuman animals, it nonetheless emphasizes the plasticity of the brain without reducing this property into a norm of reaction. For him, plasticity en compasses the fl exibility of a trait th at is not entirely canalized either environmentally or genetically. Thus, plasticity implies cultural evolvability—the capacity of a system to un- dergo evolution, i.e. to change—because a plastic system—like the human nervous system—can react towards novel situations by modifying these situations or by adapting itself into these situations. Copyright © 2012 SciRes. 241
F. MC MANUS We are certainly at the dawn of these alternative forms of doing biology. Current research is too much gene-centered but cognitive sciences might achieve, if they embrace the construc- tivist challenge , the possib ilit y of representin g hu m an n ature not as the negation of our cultural complexity but as what grants us that very cultu ral com plexit y. This wi ll imply a ret hinking of the very structure of modern explanations of homosexuality and human nature; rethinking also the constructivist challenge. We might only hope. Conclusion In this paper I revisited an ongoing controversy within the so called “Science Wars”: the epistemological and ontological status of homosexuality. I claimed that, in t his particular chapter of the “Science Wars”, we are continually left in an explanatory impasse even when more data are collected, more rigorous experimental techniques are developed, more subtle arguments are offered and more pluralistic narratives are told. My diagnosis of the source of this impasse led me to the con- clusion that here we are dealing with a structural problem that cannot be solved with an ela borati on of ne w models and theor ies that maintain an ontology and an epistemology th at are no longer suited as an explanans of human nature in general, and homo- sexuality in particular. In the realm of biological explanations, I pointed out the ex- istence of two conserved structural features that act synergisti- cally in order to bl ock an y chance s of a f ecund dialogue betwe en humanities and biological sciences. First, the conception of homosexuality in humans as a homologous trait to homosexual behaviors in other animals, on the one hand, and, second, con- ceiving homosexuality as a normative phenomenon that none- theless can be grounded in biological causes that structure the consciousness of homosexual subjects, on the other. I also claimed that these conserved structural features, al- though consistent with an evolutionary thinking, interfere with the possibility of fully understanding the construct ivist challenge. This is so because these conserved features offer a trans-his- torical view on homosexuality that ignores the complexities of the human subject. This constructivist challenge has two more attributes. Both emanate from a criticism that deconstructs the supposed validity and objectivity of the evidence and the causal narrative erected upon it through a dialectic analysis of the relationship between the subject and the object. The ultimate goal of the constructiv- ists is to restore the complexity of the subject and, therefore, advance the possibility of searching for a different type of ex- planation. Nevertheless, my analysis of the structural features of the biological explanations and the constructivist counter-explana- tions also led me to the belief that, although biologists do not fully understand the intricacies of subjects, neither constructiv- ists understand the fact icity of evolution and the challenge that it implies. If so, then the subject m ight be the right target of explanation. And, if so, constructivists might be r ight abou t th e un iquen ess of human homosexuality as a modern, western phenomenon ex- plainable in terms of subjectivities and identities that mold and are molded b y desires and institution s. But, if t hey are, evo lution is not expendable because now we are facing a most intriguing question: How is that we humans became subjects? In my view th e r esolution of thes e te nsions r equir es refr aming the question in order to abandon the conserved structural ele- ments that anchor research. Eventually, this should takes us into a new framew ork in which we can talk of an Evo lutionar y Social Constructivism in which human nature is not represented any- more as the negation of our cultural complexity but as what grants us that very cultural complexity. Acknowledgements I would like to thank Edna Suá rez for her sup port, advices a nd encouragement. Also, I would like to thank Rasmus Winther for his support and advices. Finally, I would like to thank the seminars of Philosophy of Biology at UNAM and UAM-C and the scholarship provided by DGAPA-UNAM. REFERENCES Bagemihl, B. (1999). Biological exuberance: Animal homosexuality and natural diversity. New York, NY: St. Martin’s Press. Butler, J. (1993). Bodies that matter: On the discursive limits of “sex”. New York, NY: Routledge. Byne, W. (1994). The biological evidence challenged. Scientific Ame- rican, 270, 50-55. doi:10.1038/scientificamerican0594-50 Craver, C. (2007). Explaining the brain: Mechanisms and the mosaic unity of neuroscience. L ond on: Oxfo rd University press. Daston, L., & Galison, P. (2010). Objectivity. Brooklyn, NY: Zone Books. Dean, T., & Lane, C. (2001). Homosexuality and psychoanalysis. Chi- cago, IL: The University of Chicag o Press. DeLamater, J., & Shibley, H. J. (1998). Essentialism vs social construc- tionism in the study of human sexuality. The Journal of Sex Research, 35, 10-18. doi:10.1080/00224499809551913 Derrida, J. (2008). The animal that therefore I am. New York, NY: Fordham University Press. Dickinson, N., Paul, C., & Herbison, P. (2003) . Same-sex attraction in a birth cohort: Prevalence and persistance in early adulthood. Social Science & Medicine, 56, 1607-1615. doi:10.1016/S0277-9536(02)00161-2 Esteban, J. M., & Martínez, S. (Eds.) (2008). Normas y Prácticas en la Ciencia. Mexico City: UNAM-IIF’s. Fausto-Sterling, A. (2000). Sexing the body: Gender politics and the construction of sexuality. N e w York, NY: Basic Books. Ferla, L. (2004). Gregorio Marañón y la apropiación de la homosexua- lidad por la medicina legal brasileña. Frenia, 4, 53-76. Foucault, M. (1977). Historia de la sexualidad. Mexico City: Siglo XXI Editores. Griffiths, P. E., & Gray, R. D. (1994). Developmental systems and evolutionary explanation. Journal of Philosophy, 91, 277-304. doi:10.2307/2940982 Griffiths, P. (2011). Our plastic nature. In S. B. Gissis, & E. Jablonka (Eds.), Transformations of lamarckism: From subtle fluids to mo- lecular biology (pp. 319- 330). London: The MIT Press. Habermas, J. (1999[1981]). Teoría de la Acción comunicativa. Racio- nalidad de la acción y racionalización social. Bogotá: Grupo Santil- lana. Hacking, I. (2001). Degeneracy, criminal behavior, and looping. In D. Wasserman, & R. Wachbroit (Eds.), Genetics and criminal behavior (pp. 141-168). Cambridge: Cambridge University Press. doi:10.1017/CBO9781139173162.006 Hamer, D., Hu, S. Magnuson, V., Hu, N., & Pattatucci, A. (1993). A linkage between DNA markers on the X chromosome and Male Sexual Orientation. Scienc e, 261, 321-327. doi:10.1126/science.8332896 Haraway, D. (1989). Primate visions: Gender, race, and nature in the world of modern science. New York, NY: Routledge, Chapman and Hall, Inc. Hebb, D. O. (1953). Heredity and environment in mammalian behav- iour. The British Journal of An i m a l Behaviour, 1, 43-47. Copyright © 2012 SciRes. 242
F. MC MANUS Copyright © 2012 SciRes. 243 doi:10.1016/S0950-5601(53)80053-5 Heidegger, M. (1971[1927]). El Ser y El Tiempo. Mexico City: Fondo de Cultura Económica. Hu, S., Pattatucci, A. M. L., Patterso n, C., Li, L., Fu lke r, D., Ch erny, S. , Kruglyak, L., & Hamer, D. (1995). Linkage between sexual orienta- tion and chromosome Xq28 in males but not in females. Nature Ge- netics, 11, 248-256. doi:10.1038/ng1195-248 Hull, D. (1965). The effect of essentialism on Taxonomy: Two thou- sand years of Stasis I. British Journal for the Philosophy of Science, 15, 314-326. doi:10.1093/bjps/XV.60.314 Hutchinson, G. E. (1959). A speculative consideration of certain forms of sexual selection in Man. American Naturalist, 93, 81-93. doi:10.1086/282059 King Dávalos, P. (2008). De las normas implícitas en las prácticas lingüísticas a las normas implícitas en prácticas epistémicas. In Esteban & Martínez (Eds.), Normas y prácticas en la ciencia (pp. 61-80). Mexico City: UNAM. Kirby, J. (2003). A new group-selection model for the evolution of homosexuality. Biology and Philosophy, 18, 683-694. doi:10.1023/A:1026321628276 Kuhn, T. S. (1977). Objectivity, value judgment, and theory choice. In T. S. Kuhn (Ed.), The essential tension (pp. 320-339). Chicago: The University of Chicago Press. Latour, B. (1992). Ciencia en Acción. Cómo seguir a los científicos e ingenieros a través de la sociedad. Bar celon a: Editorial Labor. Latour, B. (1999). Pandora’s Hope: Essays on the reality of science studies. Cambridge, MA: Harvard University Press. LeVay, S. (1991). A difference in hypothalamic structure between heterosexual and homosexual men. Science, 253 , 1034-1037. doi:10.1126/science.1887219 LeVay, S., & Hammer, D. (1994). Evidence for a biological influence in Male homosexuality . Sci e nt if ic American, 2 7 0, 44-49. doi:10.1038/scientificamerican0594-44 Longino, E. H. (2002). The fate of knowledge. Princeton, NJ: Princeton University Press. Marañon, G. (1960). Ensayos sobre la vida sexual. Madrid: Espasa- Calpe. Marks, J. (2012). Evolutionary ideologies. In A. Poiani (Ed.), Prag- matic evolution: The applications of evolutionary theory (pp. 297- 312). Cambr idge: Cambridge University Press. Martínez, M., & Moya, A. (2011). Natural selection and multilevel causation. Philosophy & Theory in Biology, 3, e212. Mayr, E. (1993). Proximate and ultimate causations. Biology and Phi- losophy, 8, 93-94. doi:10.1007/BF00868508 Mc Manus, F. (2009). Rational disagreements in phylogenetics. Acta Biotheoretica, 57, 99-127. doi:10.1007/s10441-009-9072-2 Mc Manus, F. (2010). La Homosexualidad a la luz de la Filosofía de la Ciencia: Mecanismos Biológicos, Subjetividad y Poder. PhD Thesis, Mexico City: UNAM. Mc Manus, F. (in Press). Las Bases neuroendocrinas de la Homo- sexualidad y la atomización mecanística del cuerpo. Millikan, R. G. (1984). Language, thought, and other biological cate- gories: New foundations for realism. London: The MIT Press. Muscarella, F., Fink, B., Grammer, K., & Krik-Smith, M. (2001). Ho- mosexual orientation in males: Evolutionary and ethological aspects. Neuroendocrinology Letters, 22, 393-400. Oyama, S., Griffiths, P., & Gray, R. (2001). Cycles of contingency: Developmental systems and evolution. London: The MIT Press. Pillard, R. (1997). The search for a genetic Influence on Sexual orienta- tion. In V. A. Rosario (Ed.), Science and homosexualities (pp. 226- 241). New York: Routledge. Poiani, A. (2010). Animal homosexuality: A biosocial perspective. Cambridge: Cambridge Uni versity Press. Prieur, A. (2008). La casa de la mema: Travestis, locas y machos. Mexico City: PUEG-UNAM. Rahman, Q., & Wilson, G. (2003). Born gay? The psychobiology of human sexual orientation (Review). Personality and Individual Dif- ferences, 34, 1337-1382. doi:10.1016/S0191-8869(02)00140-X Rendall, D., & Di Fiore, A. (2007). Homoplasy, homology, and the perceived special status of behavior in evolution. Journal of Human Evolution, 52, 504 -521. doi:10.1016/j.jhevol.2006.11.014 Rieppel, O. (2005). Modules, kinds, and homology. Journal of Experi- mental Zoology, 304B, 18-27. doi:10.1002/jez.b.21025 Roof, J. (1992). Hypothalamic criticism: Gay Males studies and male feminist criticism. American Literary History, 4, 355-364. doi:10.1093/alh/4.2.355 Rosario, V. A. (1997). Homosexual bio-histories: Genetic nostalgias and the quest for paternity. In V. A. Rosario (Ed.), Science and Ho- mosexualities (pp. 89-107). New York: Routledge. Roughgarden, J. (2004). Evolution’s rainbow: Diversity, gender, and sexuality in nature and people. Los Angeles, CA: University of Cali- fornia Press. Roughgarden, J. (2009). The genial gene: Deconstructing Darwinian selfishness, cooperation and the evolution of Sex. Los Angeles, CA: University of California Press. Rouse, J. (1994). Engaging science: How to understand its practices philosophically. New York, NY: Cornell University Press. Rouse, J. (2002). How scientific practices matter: Reclaiming philoso- phical naturalism. Chicago, IL: Chicago University Press. Savic, I., Berglund, H., & Lindström, P. (2005). Brain response to putative pheromones in homosexual men. PNAS, 102, 7356-7361. Savic, I., Berglund, H., & Lindström, P. (2008). PET and MRI show differences in cerebral asymmetry and functional connectivity be- tween homo- and heterosexual subjects. PNAS, 105, 10273-10274. doi:10.1073/pnas.0407998102 Schmitt, F. (Ed.) (1994). Socializing epistemology: The social dimen- sions of knowledge. New York, NY: Roman and Littlefield. Sober, E., & Wilson, D. S. (1998). Unto others: The evolution of psy- chology and unselfish behavior. Cambri dge, MA: Harvard University Press. Sterelny, K. (2001). The evolution of agency and other essays (Cam- bridge Studies in Philosophy of Biology). Cambridge, MA: Cam- bridge University Press. Striedter, G. F. (2004). Principles of brain evolution. Sunderland, MA: Sinauers Associates, Inc. Sullivan, N. (2003). A critical introduction to Queer Theory. New York, NY: New York University Press. Swaab, D., Chung, W., Kruijver, F., Hofman, M., & Ishunina, T. (2001). Structural and fuctional sex differences in the human hypothalamus. Hormones and Behavior, 40, 93-98. doi:10.1006/hbeh.2001.1682 Vidal, F. (2006). The sciences of the soul: The early modern origins of psychology. Chicago, IL: University of Chicago Press. Weiss, G. (1999). Body images: Embodiment as intercorporeality. London: Routledge. Wilson, D. S. (2005). Evolutionary social constructivism. In J. Gotts- chall, & D. S. Wilson (Eds.), The literary animal: Evolution and the nature of narrative (Rethinking Theory) (pp. 20-37). New York: Northwestern University Press. Winther, R. (2006). On the dangers of making scientific models onto- logically independent: Taking Richard Levins’ warnings seriously. Biology and Philosophy, 21, 703-724. doi:10.1007/s10539-006-9053-7 Winther, R. (2009). Character analysis in cladistics: Abstraction, reifi- cation, and the search for objectivity. Acta Biotheoretica, 57, 129- 162. doi:10.1007/s10441-008-9064-7 Yamamoto, D., Ito, H., & Fujitani, K. (1996). Genetic dissection of sexual orientation: Behavioral, cellular, and molecular approaches in Drosophila melanogaster. Neuroscience Research, 26, 95-107. doi:10.1016/S0168-0102(96)01087-5
|