Thursday, August 16, 2012

An Epistemology of Gender

This is my Master's in Anthropology Thesis - Submitted and Accepted in 1988.

In the 25 years since I wrote this the advances in state of the literature is nothing short of phenomenal. I will eventually revisit this work to bring it up to date. However, I believe that overall - the thesis still stands up, and I thought I would share it.

Preface – Personal Foundations

In many ways the thoughts and views reflected in this work represent a personal odyssey that has involved more than the acquisition of objective intellectual understanding. Intricately embodied in this endeavour has been a striving for emotional and psychological growth and development. It can be said that the nature of the topic makes it impossible to separate oneself as a dispassionate observer whose subject matter has no bearing or influence on the rest of one's life or conduct. The intertwining of observer and subject matter can have some positive benefit in that the considerations and consequences of findings may more easily be practically grounded. However, for beneficial results to be derived from such a complex area of study the observer is required to confront and acknowledge the belief and value systems constituting the observational base.

The introduction of one sort of bias or another into one's work cannot be avoided. The best precaution is to make as explicit as possible the potential sources of bias. With this in mind it may be important to elaborate some of the personal background pertinent to the present study.

Among the idiosyncrasies of my own upbringing was the fact that I was raised by two women – my mother and her mother (my grandmother). Each woman played different roles in a unique sort of family structure and each taught me different things. It was from my grandmother that I learned how to use carpentry tools, yet neither woman went out of their way to ensure I knew how to cook or launder. In retrospect, I am able to discern some behaviour patterns exhibited by both women that may have been due to the difficulties they faced as women having to be independent in a society in which independent women were not the norm. In the process of growing up I was aware of inequality in the hierarchy of social stratification, but not especially of the inequality of women. In fact many of the images of competence that I continue to carry are of these two significant models of independence.

As an adult I became conscious that economic, social, and psychological dynamics were important factors shaping my experience and ultimately my identity. A fundamental source of self-consciousness is of course the relating we participate in. The rudimentary categories of relationship that I was able to initially distinguish as important were based on distinctions between: 

1.       Classes (which included differences in family structure and dynamics, as well as other socioeconomic factors);
2.       The different quality of relations occurring because of the sex of the participants; and
3.       The different statuses of the participants (for example parent-child or friend-friend).

Becoming cognizant of different categories of relationship permitted the discernment of relational patterns, both within and between categories of relationship. The capacity to discern relational patterns was the primary origin of the motivational curiosity that served as the background for the present work. Specifically, what had seemed to be relational patterns unique to the experience of my parents were apparently being recreated in my own experience despite my best efforts to ensure the opposite. These "inherited" relational patterns were initially most evident to me in my own attitudes and expectations of women.  Eventually I became conscious of corresponding patterns in my attitudes and expectations in other categories of relationship including those to other men, authority figures, social and cultural groups other than my own, and to other classes of social situations.

The sort of inheritance and apparent re-creation of familial relational patterns speak strongly in favour of those views founded on theories proposing the socially constructed nature of identity (including gender characteristics). The innumerable diversity of differences between individuals can be seen as a partial result, at least, of the inevitably unique histories of every individual. Yet the issue is not so simple! This point will be assumed as a given throughout this work and pertinent to every point of view.

Having dedicated approximately eight years of my early adult life to the exploration and establishment of alternative life styles and values, I have been able to experience and observe a good many individual and group efforts to change traditional patterns of behaviour and expectations. The many challenges, opportunities and insights that were integral to this period of my life continue to present themselves, both as a set of resources and an experiential base to reflect upon. Despite the realization that the transformation of tradition (in the profound or even radical way that many in my generation hoped to accomplish) proves impossible, many deep changes have been forthcoming. The view of the social construction of personality/identity would seem to find much support in the observations during this period of "social experiments." However, several areas of experience seemed to tap into roots that extended beyond the parameters of society and culture. Certainly, the particular manifestations of our experience as humans are never free from social or cultural influence. Yet, the source of many experiences may not be found in cultural determinants, but rather in the transcultural determinants of the human condition itself.

Chief among the areas of experience that seems, to this eye, to expose some transcultural aspects of the human condition, is that area of experiential dynamics concerning sexuality and reproduction. While many of the dynamics involved in the reproductive process are necessarily culturally specific, I felt that there were different classes of existential motivations or decisions initially available to each sex. However, accepting a transcultural difference in the orientation of the relational attitudes of each sex does not require an inevitable acceptance of differences behavioral capacity. Despite differences in perceptual orientation an assertion that both sexes share a common behavioral repertoire can be well founded in a general and overriding human capability. Thus, both differences and similarities can be viewed as having a transcultural base. Culturally specific manifestations of both similarities and differences depend on many systemic factors, adaptational systems being only one.

What is more to the point, are the types of choices available to a person in the midst of an existential crisis concerning individual purpose and belonging, especially as they relate to potential reproductive involvement. Perhaps, in more than any other area of human experience, are the implications relevant to differences between the sexes more easily discernible. The experiences, both personal and observed surrounding this issue has been a fundamental factor inspiring the development of this thesis.

The thesis embraces several theoretical frameworks, from biological to symbolic. Anthropology is perhaps the most appropriate discipline within which to carry out this study. The reach of anthropology, extended through its many sub-disciplines, is able to grasp the pertinent theoretical frameworks as well as to provide a perspective based on cross-cultural knowledge.

Chapter One – Epistemological Frameworks

It is increasingly clear that our cultural values have been undermined, so that even among the masses, and especially among today's youth, there are individuals who are seeking, not so much the destruction of the old, as something new on which to build. And because the destruction has been so widespread and has gone so deep, this new foundation must be located in the depths in the most natural, the most primordial, most universally human core of existence. 
Marie-Louise von Franz, (1975) 

The development of a comprehensive understanding of human behaviour is rife with problems, especially if such an understanding remains based solely on personal experience. However, the other side of the coin is the problematic of objective knowledge. The subjective-objective basis of knowledge has been a fundamental issue in the controversy (and confusion) concerning sex and gender. On one hand there is the much substantiated claim that our language (and our social structure) privileges the male, notably in the guise of an objective and universal science. On the other hand, the recognition of subjective experience such as the "problem with no name" (Friedan 1963), made easier through the practice of consciousness raising groups, has played a significant role in the contemporary development of the feminist movement. The continuing feminist challenge to the prevailing social and scientific paradigm has contributed a great deal to the formulation of a more adequate conception of human nature.  However, a number of problems remain. The purpose of this study will be to elaborate a useful theoretical frame within which some aspects of the study of sex differences and similarities and the social construction of gender can be carried out. The proposed frame will incorporate developmental, evolutionary, historical, culturally specific and transcultural observations and perspectives. The frame will aim to avoid the fallacy of the bifurcation of nature by stressing a mind-body unity that acknowledges sex-specific differences within a context of an overwhelming similarity of behavioral potential among individuals of our species. Naturally, the caution against the reification of theory applies to this thesis.

A relatively well accepted view asserts that perception is contingent on some sort of figure-ground relationship. Accepting this as a proposition, it is then possible that the perception of individual differences as 'figure' presupposes a 'ground' of overriding similarities. For example, the not uncommon experience that individuals belonging to an unfamiliar race (or perhaps family) "all look alike". Only after the perceiver has become familiar with the overall similarities of the particular group does a host of subtle and not so subtle individual differences emerge to perception. Thus, a factor contributing to the perception of individuality (in behaviour and development) is a contextual "ground" of similarities. In fact we may be able partially to define "culture" as the determiner of the contextual "ground" of similarities (behavioral and otherwise) out of which emerges individualities. Other factors would include the spectrum of norms that provide the parameters of possible differences.

Fundamental to this study is the view that reality is essentially process and pattern (of organizing information, and information in turn being "news of difference") (Bateson, 1979). To this end some of the perspectives of C.G. Jung, G. Bateson, C. Laughlin et al, E. Count, Varela & Maturana, systems theory and others have been instrumental and are integrated in the construction of our theoretical frame.

Perhaps a central source of problems lies in what Gregory Bateson (1972) has termed pathologies of epistemology, which includes the fallacy of purposive or objective thinking. The consequence of purposive thinking, as a methodology for problem solving, is its linearity of focus almost guarantees the development of "side-effects". The potential of purposive thought to generate certain types of misunderstanding may be compounded by the Indo-European languages. While a full examination of the influence of language is not within the scope or intent of this work, a brief elaboration is appropriate and useful.

The nominalization of processes, that is the extended reliance of our language on nouns, tempts us into the "naturalization" of the fallacy of misplaced concreteness. For example, we often speak of wanting a good or better relationship. While we implicitly understand that "a relationship" as such does not exist in the same way that a "thing" does, we generally act as if the "relationship" were a "thing." We use the noun "relationship" to describe succinctly the type or types of relating that are actively being maintained.  However, when a relational problem is framed as "the relationship is not satisfying" then an obvious solution is to "get out of, or leave the relationship" as if it were a thing. Such a solution seems to be obvious and straightforward, centering the problem objectively – that is without a subject. However, when a relational problem is framed as "the way I'm relating is not satisfying" then the subsequent solutions become focused on the behaviour of the subject, that is, on changing the way I relate. While both solutions may ultimately appear to be identical, the process by which the solution was arrived at, through the later approach and the potential for alternatives contained therein seems to hold, by far, more choice and flexibility.

It is very difficult, as a natural speaker of English and French without fluency in any other language, to conceive of speaking or thinking without the use of nouns. Nouns appear to have played a very useful role as conceptual tools in the development of the knowledge systems that dominate our culture. Despite the aim of maintaining a systemic approach it will be impossible to avoid the nominalization inherent in the language.

No aspect or process is free of being "nominally reified". It is especially important to remember this when we are conceptually framing living systems. In the social sciences much confusion has been created through the nominalization of living processes. For instance, there is the conceptual trap in thinking of the evolution of individual traits or characteristics. This type of conceptualizing often leads to an understanding of discrete parts rather than functioning wholes.  The idea of traits has been applied to a range of theories, from the evolution of species to the development of personality, (including of course notions of gender, masculinity and femininity, etc.). It is the aim of this work to avoid these sorts of conceptual problems. Toward this end, Count's (1973) view that it is systems and not traits (nominalized processes or systems of processes) which evolve, will be adopted.

Another major source of confusion in the thinking concerning sex and gender (and perhaps the social sciences in general) is the lack of consideration of the complex levels in the nature of living experience. If we assume that human experience is multi-leveled we can proceed to make some distinctions between certain of these levels. A logical place to begin in making distinctions between different levels is by defining the terms sex, gender, and sexuality, since I believe they are often erroneously used interchangeably.

In higher life forms only two sexes exist. In virtually all vertebrates and mammals the life cycle can be divided into two phases; a reproductive and a non-reproductive phase. Generally speaking sex becomes a significant determiner of behaviour only during the reproductive phase (Count 1973). On this level, sex functions to ensure the survival of the species by providing the mechanism for reproduction and evolutionary adaptation. The neurostructures responsible for the development and functioning of anatomical or bio-physiological sexual dimorphism are complemented by neurostructures concerned with the individual's survival and existence (this will be expanded upon in chapter two). Although the picture is more complicated at the human level (as will be elaborated in the next chapter) the definition of sex as stated in the above holds true.

Gender as a term appears not to be so clear cut, and only a tentative definition is offered. Genders emerge as socially constructed categories which in turn consist of combinations of components of behaviour that are perceived as isomorphic or consistent with the sex-specific developmental and organizational patterns. While some developmental and organizational patterns are sex-specific, it must be stressed that gender categories do not depend on one's sex as much as on one's behaviour and sometimes status (for instance, in some cultures infants and the elderly are referred to as "its" (Cove 1987 personal communication)).

Sexuality or "polymorphous pleasure"[1] is both problem and solution embodied in the evolutionary experiment represented by the human species. Sexuality may be briefly defined as the "freeing of the libido" made possible by the evolution of the menstrual cycle and the more encompassing homeomorphogenetic relation between body morphology and the hierarchically organized structures of the brain and nervous system. Sexuality becomes more particularly a function concerning the individual rather than the species. A more complete articulation of the nature of human sexuality will be presented in the next chapter. Thus far, our definitions permit us to posit that from two sexes are born the potential for multiple gender categories and innumerable sexualities or varieties of sexual behaviour.

Another fundamental concern, central to an understanding of the unity and distinctiveness of levels within living systems, as well as to proponents of theories of the socially constructed nature of gender, is how the subject is conceptualized. A host of different psychological perspectives acknowledge, in one way or another, the myth of the "unitary, rational, homunculus" (Henriques, Holloway, et al, 1984). This study's perspective takes as given that the socially constructed nature of the subject (as a personality) is incontrovertible. However, a major problem remains. If the subject is neither unitary, nor rational, then upon what do we hang the notion of the individual? It may be that the concept of 'the individual', which we in our culture understand to be a ubiquitous reality, can itself be a social construction.

Berman (1984) speaks of the emergence of an "objective consciousness" sometime between the 1300's and 1500's and established throughout the West in the 1700's. Today, our culture considers objective consciousness to be so much the natural order of things that any other form of consciousness is thought of as an altered state of consciousness. Of course a cultural position that considers all but 'objective consciousness' an 'altered state' can in turn be seen as oriented toward a "monophasic consciousness" (Laughlin 1978, 1983). Be that as it may, what may be important to the conceptualization of the individual is the objectification of experience. The observer in seeing/creating objects easily habituates the perception of a sort of continuity-in-autonomy as a singular, unitary identity/ego/individuality. Extended to a more inclusive level this perception of a continuity-in-autonomy can lead some to the experience of the Transcendental Ego.

The theoretical view of living systems (distinguishable from other systems by their apparent autonomy) developed by Maturana and Varela (1980, also Varela, 1979) serves as a useful epistemological foundation. Upon this perspective we can not only "hang" the phenomenology of a unitary subject, but also certain aspects of the phenomenologies concerned with different levels at which living systems function, (i.e. the ecology as a whole, a particular species, individual females or males etc.). This theoretical framework is also important in that it elaborates a relationship between phenomenological, biological and ontological processes of an organism without using the dualism that so often separates mind from body. The distinction between behavioral capacities and phenomenological/physical unities is vital if we are to achieve a useful understanding of sex similarities and differences. Furthermore, the establishment of an epistemological foundation out of which gender is socially constructed depends on a framework that can distinguish between behavioral capacities and bio-neuro-physiologically linked phenomenologies if we are to respect sex differences without prescribing behaviors that are confining or inappropriate.

A brief reiteration of their views concerning living systems may be appropriate at this point. Maturana and Varela (1980) in speaking of the development of their work state:

What was ...fundamental was the discovery that one had to close off the nervous system to account for its operation, and that perception should not be viewed as a grasping of an external reality, but rather as the specification of one, because no distinction was possible between perception and hallucination in the operation of the nervous system as a closed network (Maturana and Varela, 1980:XV).

Furthermore the authors (1980:7) contend that cognition can only be understood when it is considered a biological phenomenon and that, "any epistemological insight into the domain of knowledge requires this understanding." These theorists describe their understanding of a cognitive system in the following statement:

A cognitive system is a system whose organization defines a domain of interactions in which it can act with relevance to the maintenance of itself, and the process of cognition is the actual (inductive) acting or behaving in this domain (Maturana and Varela 1980:13).

Thus a cognitive system is a living system and living and cognition are the same process. This is true of all organisms whether they have a nervous system or not. The nervous system does not create cognition but expands the cognitive domain by making interactions with pure relations possible (Maturana and Varela 1980:13).

However, this brief presentation of a theory of cognitive systems is incomplete without the encompassing theory of living systems that has been developed by the same authors. The importance and significance of the implications of their perspective, for this work and the social sciences as a whole, should not be measured by the brevity of the following synopsis.

Maturana and Varela (1980:48) offer a summary of a concept of the organization of living systems in the following:

The living organization is a circular organization which secures the production or maintenance of the components that specify it in such a manner that the product of their functioning is the very same organization that produces them.

A living system is thus a homeostatic one. Such a system holds its own organization as a variable that is maintained constant, through the production and functioning of the components that specify it (as a system). Its own organization defines itself as a unit of interactions. Living systems then, are a subclass of circular and homeostatic systems (Maturana and Varela 1980:48).


However, the apparent struggle for conciseness in the above definition of the self-referential circular organization of living systems, as well as the potential for misunderstanding involved in using a language developed to frame other conceptual systems, led the authors to the realization that coining a more specific term would be necessary.  Their choice was the term "autopoiesis" from the Greek auto = self, and poiesis = to produce, that is self-producing. Thus:

An autopoietic system is organized (defined as a unity) as a network of processes of production (transformation and destruction) of components that produces the components that: (1) through their interactions and transformations continuously regenerate and realize the network of processes (relations) that produced them: and (2) constitute it ... as a concrete unity in the space in which they exist by specifying the topological domain of its realization as such a network. (Varela, 1979:13).

Perhaps the self-referential circularity of an autopoietic identity is most succinctly framed by Popeye's statement, "I am what I am that I am what I am."

Autopoietic systems can be further defined as autonomous. As self-producing systems they subordinate all changes to the maintenance of their organization, no matter how profoundly they may otherwise be transformed in the process. Furthermore, autopoietic system can be said to have individuality. Holding its organization as an invariant through its continuous production, an identity is actively maintained which is independent of its interactions with an observer (Maturana and Varela 1980:80).

Accepting the definition of autopoietic systems, we have a substantial transcultural base upon which the phenomenology of a unitary (if not rational) "homunculus" can be placed. Additionally, this base permits us to elaborate a phenomenology/cognition that is relevant to an autonomous identity yet which is dependent on a particular structure and organization. More significantly, by linking structure and ontology with a consequent phenomenology, the theory of autopoiesis is a particularly appropriate framework with which to understand each sex individually as well as an interactional mutualism of one species. We will argue that the structural and ontological differences between each sex are exemplified in corresponding patterns of perceptions and cognitions.

As unlimited in content or form that the phenomenology of a living system can be, the authors (Maturana and Varela 1980:97) do note some stipulations.  Included in these concerns are:
  1. Since autopoietic organization defines the system as a unity, the implication is that the phenomenology of the system is totally subordinated to the maintenance of its unity.
  2. A particular unity defines the domain of its phenomenology. However the specific structure constituting the unity defines the kind of phenomenology that is generated in that domain. That is the particular form adopted by the phenomenology of each autopoietic unity depends on the particular way in which its autopoiesis is realized.
  3. Finally, all biological phenomenology is determined and realized through individual autopoietic unities and consists of all the paths of transformations that homeostatic systems undergo, singly or in groups, in the process of maintaining their defining individual relations constant.
In making the point that individual phenomenology is determined and realized by all the paths of transformation undergone by an autopoietic system (in biological form) these authors are paving an introduction to an understanding of the significance of ontogeny. However, before we can pursue the topic of ontogeny further one more vital consideration regarding the phenomenology of autopoietic systems needs to be discussed.

The circularity of the autopoietic system has very important implications for an understanding of its phenomenology. More specifically the nervous system interacts only with relations that are necessarily mediated by physical interaction.  The objects seen by an animal are not determined by the quantity of light absorbed, but rather by the relations that hold between the receptor induced states of activity within the retina. The types of relations that are possible are determined by the connectivity of the various types of cells involved. Therefore, "the nervous system defines through the relative weights of the patterns of interactions of its various components, both innate and acquired through experience, which relations will modify it at any given interaction" (Maturana and Varela, 1980:2). In general, the organization and structure of an autopoietic system define in it, a bias, a point of view or perspective from within which it interacts, by determining at any instant the possible relations accessible to or generated by its nervous system. By outlining some of the major structural and ontological differences unique to each sex we will present the corresponding biases, or perspectives.

Additionally, organisms exist which include as a subset of their possible interactions, interactions with their own internal states (resultant from external and internal interactions) as if these were independent entities. On this basis we can understand the impossibility of determining perception from hallucination in the operation of the nervous system as a closed network. An apparent paradox emerges as an organism can include their own cognitive domain within their cognitive domain (Maturana and Varela 1980:13). However, this may be the basis of the occurrence of such phenomena as "symbolic penetration" (Webber, 1980; Webber and Laughlin, 1979) which in turn can serve as a methodology for the development (cultural or otherwise) of more comprehensive and complex cognized environments and perceptual filters.

The phenomenology of the nervous system is exclusively that of the changes of state of a closed neuronal network such that for it there is no inside or outside. The specification of boundaries making possible the distinction between internal and external origins of changes of state of the nervous system can only be made by an observer beholding an organism as a unity. Thus, state changes of the nervous system can only originate internally or externally in respect to the domain of interactions of the organism as a unity. Therefore, "the history of the causes of the changes of state of the nervous system lies in a different phenomenological domain than the changes of state themselves" (Maturana and Varela 1980:128).

Given that all states of the nervous system are internal states and that in its process of transformation the nervous system is unable to make distinctions between internally and externally generated changes, then it is equally likely to couple its history of transformations to the history of its internally and/or externally determined state changes. "Thus the transformations that the nervous system undergoes during its operation are a constitutive part of its ambience" (Maturana and Varela 1980:131).

The position taken in this paper relies on the significance of development as a lifelong process. More accurately it posits that, despite individual differences and similarities and the assumption that individuals of the human species are in a general sense capable of exhibiting the entire spectrum of behaviour available to the species as a whole, there remain sex-specific developmental patterns responsible for correspondingly different perceptual orientations. Ontogeny then, "is the history of the structural transformation of a unity. Accordingly, the ontogeny of a living system is the history of maintenance of its identity through continuous autopoiesis in the physical space" (Maturana and Varela 1980:98).

More significantly, the cognitive domain of any autopoietic system is relative to the specific manner in which its autopoiesis is realized. Knowledge (as descriptive conduct) is then to be considered as relative to the knower's cognitive domain. The knowledge of an organism (its conduct repertoire) changes as the manner in which its autopoiesis is realized during the ontogeny, also changes. Therefore:

…knowledge, then is necessarily always a reflection of the ontogeny of the knower because ontogeny as a process of continuous structural change without loss of autopoiesis is a process of continuous specification of the behavioral capacity of the organism, and, hence, of its actual domain of interactions (Maturana and Varela 1980:119).

The consequence of this view is that absolute knowledge is not possible and the validation of all possible relative knowledge is achieved through successful autopoiesis (Maturana and Varela 1980:119). The idea important to note is that ontogeny can occur only because of the maintenance of identity throughout continuous autopoiesis, and that the knowledge of the knower is dependent on the knower's ontogeny.

Another issue fundamental to the foundation of the ideas being developed in this work concerns the bridge between the behavioral parameters circumscribing the individual and those circumscribing the species. Without using such problematic notions as instincts, etc. Maturana and Varela (1980:109) offer their conceptual bridge in the following:

An autopoietic system whose autopoiesis entails the autopoiesis of the coupled autopoietic unities which realize it, is an autopoietic system of a higher order.

When an autopoietic system of this sort of higher order occurs, the way in which the component autopoietic systems realize their own autopoiesis becomes subordinated to the maintenance of the autopoiesis of the higher order (composite) autopoietic unity (Maturana and Varela 1980:110). The higher order autopoietic unity is defined topologically through the coupling of component autopoietic unities. In reference to evolution, the same sort of relations, hold between component and composite autopoietic unities. The authors state:

If the higher order autopoietic system undergoes self-reproduction (through the self-reproduction of one of its component autopoietic unities or otherwise), an evolutionary process begins in which the evolution of the manner of realization of the component autopoietic systems is necessarily subordinated to the evolution of the manner of realization of the composite unity (Maturana and Varela 1980:111).

The conceptualization of autopoietic systems as living unitary systems, which can in turn be composed of, or be a component of autopoietic systems of different orders, sets a frame within which both the individual and the species can be viewed and described in equal terms. However, the hierarchy of different orders of autopoietic systems places certain constraints on the priorities that can be established within each of these different orders of autopoietic systems. Stated succinctly it is only after becoming constituted as an autopoietic unity (individual) that reproduction can take place as a biological phenomenon (Maturana and Varela 1980:97). It follows that the human species must therefore be an autopoietic unity and that individual males and females are composite autopoietic unities. In turn, the realization of the autopoiesis of females and males is subordinated to the maintenance of the autopoiesis of the species. We can discern two important consequences from this view:
  1. Although male and female may contribute equally in the maintenance of the autopoiesis of the species they would logically contribute differently (or two sexes would be redundant); 
  2. From the perspective of an individual, the perceptual/cognitive experience of this species serving dimorphism would likely involve certain aspects of a transpersonal phenomenology. 
The remaining concern, important to this paper, and addressed by the theory of autopoiesis is the dynamic of the communication between individual organisms. The complex position regarding communication that is maintained by Maturana and Varela (1980:120) is summarized in the following. A recursive or expanding domain of communicative interactions is generated, as interlocked ontogenies constituting together a domain of mutually triggering consensual conducts which in turn become specified during the ongoing process of interacting. A linguistic domain then can be defined in autopoietic terms as a consensual domain of communicative interactions arising from the coupling of the ontologies of otherwise independent autopoietic organisms whereby the organisms mutually orient to each other with behavioral modes that have been internally determined and specified during their coupled ontogenies. A linguistic domain or the component communicative and linguistic interactions are intrinsically non-informative despite the ability of an observer (if he overlooks the internal determination of the autopoiesis which generates the domain) to describe such interactions as if they were. This is particularly pertinent to the ideas presented in chapter four concerning the separation of the sexes by a common language which in turn conceals the sex-specific perceptual orientations. Maturana and Varela (1980:120) state:

Phenomenologically the linguistic domain and the domain of autopoiesis are different domains, and although one generates the elements of the other, they do not intersect.

Although the model of autopoiesis is an extremely useful conceptual tool or frame of reference with which to view living organizations, care must be taken to understand that the particular applications presented in this study requires a good deal of simplification. In the following chapters the shifts to conceptions of different orders of autopoietic systems do not account for all of the exponential increases in the complexity that higher orders of autopoietic organization incur.

There are other theoretical frameworks useful to the perspective taken in this project, which will be referred to throughout the work. Time, however, does not permit as full an elaboration of each theoretical frame as has been given to the theory of autopoiesis.

The controversy concerning sex differences has essentially been a special case of the more encompassing nature-nurture dilemma. There has always been a powerful current of biological determinism in the thinking on human behaviour (Bleier, 1984:5). Perhaps it may be that the kind of functionalism which attempted to ground behavioral prescriptions upon a biological base fostered a reaction stressing a proportionately greater emphasis on the social-construction of gender. Either of these types of apparently one-sided approaches must be avoided.

In this regard, autopoiesis is a powerful analytical tool by which understanding and perspective of different orders of self-producing and reproducing living systems can be achieved. Furthermore, autopoiesis recognizes the significance of both hierarchical ordering and complex associative networks in the contextual circularity of the organization and structure of a living system. The profound beauty of autopoietic conceptualization is that it offers an epistemology that can encompass both male and female perceptual and cognitive orientations (as exemplified in the first section of chapter four). By extension, the conception of institutions or bureaucracies as autopoietic systems would require that their management, development and evolution be structured and organized in terms of both networks and hierarchies.

This work takes as given, that biologically based behavioral prescriptions are untenable. An approach that puts greater emphasis on the social construction of gender implies that social change can be enacted through the motivation of a collective will to do so. However, it may also exacerbate the problem in that it may tempt and even foster the projection of feelings of frustration, victimization, blaming and anger, etc. should social change not be as readily forthcoming as anticipated.  Furthermore an exclusively social constructionist approach may tend to obfuscate the complex involvement, which biological differences (and similarities) may have, in the construction of the social parameters out of which gender categories are constituted. Besides the limitations already noted, there remains the problem of developing a theoretical understanding optimising the potential for developing and instituting more appropriate social policies and structures. Thus the problem centers on how to acknowledge both the influence of biological referents of the differences between the sexes and the equality of the repertoire of behavioral potential of both sexes.

A case will be made presenting:
  1. Gender as a social phenomenology constituted out of a symbolic template derived from a species-serving sex dimorphism;
  2. A distinction between the neural (or autopoietic) structures of the species and the individual, enables the acknowledgement of biologically based sex-specific perceptual filters and consequent cognitive orientations in addition to the simultaneous potential for the integration of differing orientations.  
The autopoietic concepts elaborated in this chapter allow us to view the structural and ontological processes underlying human biological dimorphism as the foundation of a symbolic template out of which gender categories and knowledge develop. To put it more simply, being female or male is not a static state of being, rather it is [a becoming] to be, within a developmental unfolding process. Individuals experiencing such sex-specific morphological development, are from conception to death perceiving beings.


Chapter Two – Evolutionary Context: The Human Species as a Being and Becoming

A prerequisite to theorizing human experience is the outlining of the context within which that experience is shaped. Fundamental to most of the thinking on the human species is the elaboration of how and why humans are different from all other forms of life on earth. Evolutionary theory has made much of traits considered uniquely human such as the opposable thumb, an erect posture, the neocortex, speech, and symbol and tool making, etc. However, it has already been noted that evolution conceptualized in terms of morphological traits is neither accurate nor generally useful. Evolution is more comprehensively conceived with the view that it is systems which make novel adjustments rather than traits which evolve. By elaborating the evolution of the human species, in terms of the evolution of the complex interrelated systems that constitute the species, we can establish a metacontext within which the multileveled functionings of human sexual dimorphism can be understood.

To visualise the evolution of a complex system is perhaps not possible without the right set of conceptual tools. Theorizing in terms of traits and linear causal models inevitably leads to the sorts of dilemmas whereby concern is focused on the determination of origins – which comes first the chicken or the egg? Of course the chicken and the egg are one and the same autopoeitic entity at different stages of ontological transformation. The dilemma is a false one.  What emerges is a novel system, not a new thing. Autopoietic systems cannot become established in a gradual process, because it is defined as a system, that is, as a topological unity, by its very organization. A system is an autopoietic (living) one or it is not. Structural changes can occur in response to environmental perturbations, but such changes must be subordinated to the maintenance of the system's identity as an organization.

An important conceptual tool has been offered by Laughlin (1986:134135) in the explanatory causal principle of homeomorphogenesis. This principle refers to an inter-causal isomorphism between two or more changing subsystems within the same system. While total isomorphism is rare in the world, a partial isomorphism functions in a way where set A can be mapped onto set B but not vice versa. The correspondences are causally linked but they are not the same. In a sense, homeomorphogenesis names the process by which a living system maintains the homeostasis of its 'organization' through the production and functioning of its components (including its own organization as variable or component which must also be maintained constant), while undergoing structural changes or transformations. Since autopoiesis implies that all change in such a system is subordinated to the maintenance of the organization which defines it as a unity, then a change in one component may necessitate relatively isomorphic accommodations in other components as well as in the network of productions of components. Homeomorphogenesis is the process by which novelty in one aspect of a living system, orders via the system's organizational networks, isomorphic changes in other parts or subsystems.

The understanding of evolution posited in this chapter relies heavily though not exclusively on the principle of homeomorphogenesis. A case will be made to show that the human neurological capacity for symbolopoesis (the symbol making process understood as a neuropsychological phenomenon) (Count, 1973:219) is isomorphic with the relational potential embodied in the unique sexual dimorphism of humans. More specifically we will concentrate on the relational potential made possible by the evolution of the human menstrual cycle and some corresponding anatomical features (systems).

Two other theorists figure prominently in this chapter, Earl Count and A.N. Whitehead. The initial difficulty in trying to integrate different thinkers lies in the merging of each thinker's language and sphere of interest into one framework. However, the fundamentals of autopoiesis are consistent with the work of Laughlin, Count, and Whitehead. This chapter will primarily utilize the perspective and language developed by Count (1973) as his work lends itself particularly well to the description of the contextual level that this chapter aims to elaborate.

Count (1973:214) asserts that no structure has significance without a functional context. Thus, the total behavioral architecture of an organism (termed by Count as its biogram) must be located within an evolutionary and ecological context in order to be comprehensively understood. One context, within which the evolution of specific biograms can be located, has been delineated by A.N. Whitehead (1929). Whitehead posits that organic (negentropic) processes cannot be understood without some sort of implicit teleological 'principle' guiding these systems toward the methodologies enabling them "to live, to live well, and to live better." Furthermore, the 'function of reason' (Whitehead 1929) is presupposed to be applicable to all orders of systems (organic and inorganic). This thesis accepts Whitehead's notion to be operative in the shaping of successful evolutionary trends, whatever the order or level of the evolving system.

It may seem that the function of reason is incompatible with the Darwinian position on natural selection as well as Maturana and Valera's (1980 see also Valera 1979:70) view that the definition of living systems does not necessitate teleological notions. However, the explanatory principles of natural selection and the function of reason may be seen as mirror images reflecting different perspectives. Ultimately, the products of natural selection can be found to be indistinguishable from the results of the function of reason (as put forth by Whitehead, 1929).

Count (1973:221) grounds his emphasis of context by asserting that:
…the minimum completely viable universe of discourse (unit of survival) is that of organism-within-environment; anything less is an arbitrary abstraction which is useful only temporarily, and intolerable beyond some point.

The compatibility of Count's position with autopoiesis is maintained when we understand that the organism-as-system is a subsystem or moiety of the coupling "organism-environment" which in turn can refer to different orders of autopoietic systems, i.e. "organism vs. species" and "species vs ecology."

It is possible to refine the concept of organism-in-environment in terms that are appropriate to the working of species as an autopoietic system consisting of two homeomorphogenically related component autopoietic systems: "male" and "female." The adjustment occurring at the juncture of two generations is greater than that of an organism to a mere environment. Rather it is two organisms expressing a mutualism (Count, 1973:43). On the level of phylogeny, reproductive modifications must be simultaneous and complementary in both sexes. What is changing, is a system (the structure but not the organization of an autopoietic system) and not just one type of body form (Count 1973:45).

Count's concept of species biograms can also be consistent with the notion that an autopoietic system's phenomenology is dependent upon its structure. More specifically, Count (1973:221), holds that living systems organize an Umwelt through the execution of ontogenic choices. He maintains (1973:143), that an organism's life mode is representative of the externalised functionings of its morphology, the life mode evolving as a feature of the total morphologic evolution. Organisms possess a total behavioral (biogram) as well as a total physical architecture (Count 1973:72).

The elaboration of a biogram begins with a functional distinction between those processes concerned with the wellbeing of the individual and those life processes by which the individual propagates its kind (Count 1973:15). The vertebrate biogram can be viewed as being primarily engineered on a diphasic basis: a phase of reproductive quiescence and a phase of reproductive activity. Each phase takes place under a distinct endocrine or hormonal presidency activated by innate neuro-psychic mechanisms and marked by peculiar behavioral patterns. A migration that is always 'psychological' if not always physical takes place for each phase. The phases persist regardless of the gregariousness or the solitariness of the life habits of the individual (Count 1973:167).

Count (1973:30) offered the generalization that specialized adaptations of an animal's life mode are effected during the non-reproductive phase. Only after the non-reproductive life mode has been remodeled, is the reproductive life mode brought into the new adjustment. In behavioral terms it would seem that the non-reproductive phase of the vertebrate biogram is the most flexible. In fact very little has been studied about this phase, for instance it is not known whether: A) the intra-sex hierarchies, or B) in how far inter-sex dominances, persist. Frequently it is only during this phase that a flock will admit strangers into its membership, as the reproductive phase sees a heightened individualism (Count, 1973:567). During the reproductive phase the hitherto homomorphous society (in terms of its behaviour) develops sex moieties; while the passing of the phase witnesses the recession of this social dimorphism. Thus a realignment of social vectors and tensors, but not a cancellation, is enacted (Count, 1973:21). Animals continue to have phase specific foci of interests such that when one set is active the other tends to be inhibited, i.e. feeding and copulation do not occur simultaneously (Count, 1973:80).

While evolutionary exploration may occur in the non-reproductive phase, it may be that significant evolutionary leaps only become embodied when adaptations are integrated into the reproductive phase. An example may be the shift from oviparity to viviparity, and the subsequent change of "the autonomous male embryo with estrogenic induction of females into the autonomous female embryo with androgenic induction of males" (Sherfey, 1973:41). These types of reproductive phase changes represent radically different relations between the biogram environment mutualisms.

It is now possible to move the discussion to a consideration of the possible nature of the evolutionary question to which the human biogram is the answer. Given that the evolutionary 'unit-of-survival' is the organism-in-environment mutualism, then the onset of the reproductive phase is a question of timing the optimum environment-organism conditions in appropriate synchronous cycles. For example, in spring the exposure to increased amounts of light helps to 'warn' the organism via the pituitary gland which then stimulates the reproductive systems into assuming phasic dominance. In higher animals the instinctive patterns of the reproductive phase become triggered into action by warning mechanisms rather than by tissue hungers (Count 1973:70)[2]. Specific environmental contingencies (for instance increases in sunlight during spring) warn organisms into and through all the biogrammatic phases. However, the reproductive phase is proportionately more reliant on environmental cycles as activational contexts synchronizing phasic processes. The organism is generally freer to "boldly go" to "seek new frontiers" during the phase of reproductive quiescence.

During the reproductive phase an organism attaches its organizational homeostasis and develops a locative ego involvement with a particular "territory" and which lasts only as long as the endocrine tonus does (Count 1973:45). Among higher animals there is an increasing generality in their dependence on environmental contexts to synchronize the processes defining the reproductive phase. The organization of an organism and its Umwelt is accomplished at least partly by a process of discrimination of a self-space and an alien space. In terms of autopoiesis we can understand the discrimination of self-space to be inseparable from the maintenance of the organization defining its unity/identity. Alien space is perhaps more likely not to be as clear-cut a category. There is no specification in an autopoietic organization of what it is not. The territorialism of most animals may not be so much a differentiation of what is alien as much as a maintenance of the integrity of the particular identity[3].

Although Count (1973:251) states that alien space is further differentiated as an animal develops a territorialism of a "home" and a "range", it may be more accurate to define "home" and "range" as differentiations of the self-space since the organism adapts the physical spot to itself, as much as the converse. Alien space is exterior to the boundary of that self-identity. Count (1973:251) comments, "In fact, more than food an animal needs a focus of self-orientation. It is commonly termed 'security' by which usually is meant the emotional state of the animal that results from establishing a certain set of homeostatic conditions. "While a greater degree of flexibility attains as we move up the evolutionary ladder, the need to maintain autopoietic integrity – identity, is consistent with the establishment of sets of homeostatic conditions or more accurately, relations. It is the nature of autopoietic organization to impose its own organization as the structure of reality.

In the monkey, practically all determination and inhibition of behaviour is due to external, immediately present social forces (presence of other animals) rather than concrete environmental features (Count 1973:97). The abstraction from concrete environmental or social "warning mechanisms" is carried furthest in the human species (perhaps the cetaceans are an exception), where the importance of internalising social forces is tremendously expanded. The autopoietic position holding that the nervous system is a closed system imposing its own structure upon reality can be reconciled with the perspective that behaviour is determined by external factors. The concept of "rhythm-taking" (Count 1973, see also Laughlin, d'Aquili, McManus, et al, 1979) as the fundamental "social glue" among vertebrates is consistent with the understanding that autopoietic systems can be perturbed by independent (external) events and consequently undergo compensatory internal changes. Repeated perturbations can be compensated by repeated series of internal, though not necessarily identical changes (Valera, 1979:15). Rhythm-taking may represent a juncture between different orders of autopoietic systems.

It is widely accepted that the greatest evolutionary advantage achieved by the human species is an unsurpassed adaptability. As a species or as individuals we cannot only live, live well, etc. in almost every geographic location on the globe, but can acclimatize with relative ease from one location to another (perhaps even off the globe as well). The capacity for this agility in making an indeterminate number of ecosystems comfortably our own depends (among other things) on the isomorphic developments of our sexual and symbolizing processes.

At the human level the interests of both of the biogrammatic phases are brought into mutual relation and support (Count 1973:108). Humans differ from other vertebrates and alloprimates in the particularly rich contents that are contained within their biogrammatic framework. These contents are indicative of the influence of symbolopoetic action upon (without disrupting) the more fundamental neuro-psychic mechanisms (Count 1973:106). While continuing to share an innate grounding with lower relatives, the power to symbolize permits social generalizations, eg. eidolons (Count 1973:107). Symbolopoesis is not simply attributable to cerebral mechanisms or to neocortical function; rather, "it is profoundly a functioning of a mechanismal totality" (Count 1973:263). It will be argued that the richer content that the human has fitted into the biogrammatic framework is implicit in the human sexual dimorphism.

Included in the process of homination is the emergence of multivalent symbols and multiple statuses (Count 1973:100). Statuses can be understood as particular cases of contingencies-of-relationship involving reciprocation and permitting the development of more complex meta-categories (group statuses, statuses of statuses, etc.). An increase in the flexibility and complexity of contingencies of relationship is not simply a consequence of cerebral developments. It is one of the systemic requirements that go hand in homeomorphogenetic hand with patterned evolutionary refinements.

Bateson (1972) has proposed that the fundamental components of mammalian communication are contingencies of relationship. The development of phasia may represent the emergence of a capacity to communicate in a way, and about, other than contingencies of relationship[4]. Count (1973:216) links phasia and communication in this way:

…it is a real gain, furthermore, when phasia is recognized as being but a particularized case within the more general and comprehensive phenomenon of communication between animals, and when we recognize that we cannot hope for understanding of the particular unless we base it upon the more comprehensive.

It may be important at this point to expand upon the concepts of status, and contingencies of relationship. Statuses are defined as social generalizations. In man statuses themselves, can achieve status and thus, humans are the only species known which has the capacity to hold plural statuses simultaneously (Count 1973:148). Furthermore, status is a moiety of a dyad, a notion which comes very close to that of contingencies of relationship. Bateson (1972:3667) outlines how communication among mammals inevitably occurs in terms of patterns and contingencies of relationship. For instance, when one's cat is trying to ask for food it does so by making sounds and movements characteristic of a kitten to its mother. It would be inappropriate to translate the cat's message as a cry for milk or Meow Mix. A more apt translation would be to say that the cat is asserting "dependency! dependency!" It is the context, that is the cat's physical location in the kitchen, near the refrigerator, etc. that allows us to make the deductive leap of how the cat is dependent on us. Another context such as the door would tempt us to interpret the cat's "dependence" as a specific call to be let out[5].

It may be that the great new feature emerging out of the evolution of human language was not the ability to abstract or generalize, but the discovery of being able to be specific about something other than relationship. Despite this achievement human behaviour has scarcely been affected, as it is rare for any communicational event not to engender the devotion of a few neurons to the question of what does the communication indicate about the relationship between the communicators. 

The development of language (dependent on the capacity for phasia and symbolopoesis) may be the foundation upon which the ability to hold multiple statuses. All statuses are somehow codes which become formalized out of groups (Count 1973:148). Fluid patterns of communication utilizing contingencies of relationship can become fixed in symbol and in identity as part of an "organizational homeostasis and locative ego." The importance of status is not limited to (though it is inseparable from) communication potentials. The humanization of the primate familialism is effected by the Weiterbildung of "status" which is the cohesive of vertebrate sociality in general (Count 1973:146). By regarding the evolution of phasia, symbolopoesis, increasing complexities of social interaction etc. as homeomorphogenic complexes of systems, the foundation is laid for a clearer view of the novelty of human dimorphism.

In Count's view (1973:45) the reproductive system from ape to man has evolved hardly at all[6]. However, human sexuality in relation to alloprimates reflects a vastly more powerful information processing capacity while interrelating with a very similar "visceral" brain and a quasi-identical reproductive mechanism. In this respect Count is accurate, yet though the differences between the reproductive systems may be small, their effect is disproportionately profound. The highly significant developments of phasia and symbolopoesis with the neurophysiology responsible would seem to presume (through the principle of homeomorphogenesis) equally significant developments in human sexuality and the underlying sexual morphology and neurophysiology.

The vertebrate reproductive syndrome is always a matter of bisexual complementarity. In menstruating primates the unremitting succession of cycles is matched by a sexual constancy in the male. Thus, the male pituitary is always secreting gonadotrophic hormones with the result that the neurologic mechanisms are never without some degree of tonus due to sex hormones (Count 1973:90). As stated previously, at the human level both the non-reproductive and reproductive biogrammatic interests are brought into mutual relation and support. The interests and capabilities of the non-reproductive phase can be activated concurrently with the interests and capabilities of the reproductive phase. The reproductive biogrammatic interests are initiated by social "warning mechanisms" (the actual presence as well as the internalized representations of other humans and subsequent categories of contingencies of relationship) occurring on either single or combined levels (Count, 1973:97). In humans there is a phenomenological complexity arising as a consequence of the interfacing of different orders (including the structural particularities or dynamics of each system) of autopoietic networks. For instance, the single or combined occurrence between individuals, of types of pupillary reflexes, types of voice tones, types of situational contexts, and types of contact, age differences etc. can shift the relational emphasis remarkably.

A fundamental distinction can be made between primate and human biograms that centers on the uniqueness of the human menstrual cycle. Count (1973:89) describes the menstrual cycle as:

…a specialization of the mammalian oestral cycle, which, roughly speaking, is the symptomatic of the alternating and successive presidencies of estrogens and progesterone; reflecting a further micro-anatomical evolution. It is definitively identifiable as such only when we reach the level of the monkeys.

This description is accurate only to a point, for it misses the emergent relational potential that becomes manifest in the human. The primate menstrual cycle represents the development of a reproductive cycle that is largely independent of external concrete (except perhaps the lunar cycle) and social "warning mechanisms." While the same is true of the human menstrual cycle, there is an additional development.

With the merging of the evolutionary and exploratory flexibilities of the non-reproductive biogrammatic interests into reproductive biogrammatic modalities, sexual behaviour comes to function as a context for, as well as within the contexts of, a wide variety of categories of contingencies of relationship. More simply, sexual behaviour becomes "neocortical" in the metamorphic sense that it functions as a "field" or "stratum" within which many other areas of activity ultimately (and intimately) become associated with one another. Sex is no longer exclusively for reproduction, but becomes generalized to levels of social and individual play, communication, pleasure, etc., independent of environmental and reproductive cycles while at the same time continuing to function as a medium of social cohesion.

The discussion can now focus on a few specific examples of the distinctly human dimorphism. According to Count (1973:145) about the only distinctively human physiological feature of the reproductive system are the labia majora. Furthermore, the corresponding human perineum lacks the periodic swelling normally advertising oestrus in the female alloprimate. The human labia are best understood as predominantly a feature of the adaptive remodeling of the pelvis perineum as orthogradation is acquired. Accordingly the sexual pattern of physiological responses is not materially altered by these labia. However, the frequency of face to face copulation has shifted from its relatively low incidence among alloprimates to being almost universal in humans due, among other things, to the orthogradational remodeling.

The significance of the "orthogradational remodeling" cannot simply be restricted to raising the frequency of face to face copulation. What the new morphology permits is of the same order as "learning how to learn", that is, the significance is not additive (two sex positions instead of just one) but rather it is exponential (once there is an awareness of choice, perception can open to the potential of generating more choices). The implications of ventro-ventral copulation become much clearer when contextually located within a sexuality not limited to the reproductive syndrome. Within sexual interactions that are contextually play, communication, pleasure, etc. the potential for a great deal more complexity and information exchange in a ventro-ventral interaction is self-evident. Of course the very possibility of choice inevitably makes any specific choice a communication issue, with implications of different contingencies of relationship and even of different statuses.

In a similar line of thought Alice S. Rossi (1985:15) considers that:

…the deposition of fat during human adolescence on the breasts and buttocks is a unique feature of human sexual dimorphism that constitutes a continuous advertisement of an ability to lactate rather than a cyclic fertility advertised by oestrous swelling as do so many other higher primates.

A continuous advertisement of the ability to lactate carries a message of a contingency of relationship implying a nurturer/nurtured mutualism. Within this mutualism lies a potential for nuances of status reverberances (Count, 1973:104,131,151)[7]. Rossi's observations should also be considered in the context of a sexual morphology that is not solely limited to a reproductive syndrome. Thus, the increased erogenous sensitivity of the human breasts may be considered as homeomorphogenically related to a highly complex morphology optimising the likelihood of face to face interaction as well as enabling the potential merging of previously phase specific foci of interests such as feeding and copulation (Morgan, 1985:2830).

Taking the uniqueness of human sexuality further, Paula Weideger (1975:130) comments that:

…certainly in the human being, sex is altogether independent of reproduction in many respects. Not only as a continuous possibility of sexual intercourse, but a continuous sexuality which precedes the introduction of menstrual cycles and which continues long after menstruation has finally ceased. For the human female alone among mammalian species, sexuality is present from birth to death, (noting of course the clitoral response enjoyed from early in development).

Later Weideger (1975:139) includes a qualification with respect to the human species' distance from the strict hormonal control of sexual behaviour with a reminder that as a species, humans have demonstrated a great facility for conjuring up constraints (emotional and otherwise) that are fully as limiting and confining as any strictly physiological constraints might be. The cultural and individual variety of socially constructed constraints is indicative of both a latent behavioral flexibility, and of a relational or social matrix upon which an organizational homeostasis can be attached with the consequence of a greater independence from specific "concrete" environments. The potential for this sort of behavioral flexibility is not purely dependent on a neuro-anatomy but is implicit in human sexual dimorphism.

Thus, the pattern which connects the complex probabilistic system that is the brain as a homeomorphogenically evolved subsystem of an organism-environment mutualism, is in the nature of an implicit interlocking of sets of potentials or predispositions inherent in the morphology of both brain and sex systems. The evolution of the neocortex as an ultimate choice-maker and symbol-processor, is inseparable from and isomorphic with the evolution of a sexual dimorphism which permits a greater spectrum of intra and inter associative, and relational complexities of the organism-environment mutualism.

The human biogram may be viewed as a recent evolutionary strategy aimed at answering the necessities of living, living well, and living better. Inherent in the embodiment of this "answer" is:
  • A relative autonomy from specific environmental contingencies;
  • Complex patterns of hierarchical and non-hierarchical social relations and contingencies of relationship; and 
  • A social cohesive utilizing either or both the non-reproductive and reproductive behavioral repertoires, in sequence or simultaneously. 
In autopoietic terms, it is possible to view this social cohesive as at least partly a manifestation the dynamics inherent in a species level autopoietic system. In this view an individual (as a component autopoietic system) can experience the subservience of the realization of his/her unity to the realization of the unity of the species (as a higher order or composite autopoietic system). The processing of the information inherent in this embodied relational potential would not be possible without an equally complex, higher level of associative capacities such as the neocortex. The potential for relational complexities inherent in the human dimorphism is matched by the symbolopoetic potentials inherent in the human neuro-structure.

The present chapter has outlined some of the unique systems within the human biogram. The emphasis has been to focus on a species level understanding of human sexual dimorphism. In the following chapter we will shift our focus to an elaboration of sex specific structural and ontologic processes underlying human sex dimorphism. We will also emphasize the consequent phenomenological, perceptual, and cognitive associations as they are likely to be experienced by individuals of each sex.

Chapter Three – Defining Processes: Grounding a Symbolic Template

This chapter presents the kernel of the thesis. Sex-specific developmental patterns that are active on a continuous as well as a phasic basis will be elaborated and integrated with the theory of autopoiesis.

The notion that the processes underlying human biological dimorphism are the foundation of a symbolic template out of which gender categories and knowledge develop, requires a particular theoretical focus. The autopoietic concepts elaborated in chapter one permit both the processual and the organizational nature of biological development to be articulated. Putting it more simply it can be said that possessing a female or male body is not like possessing a static fact/noun/category, but is rather like being within a developmental, experiential, unfolding process. Sex-specific morphological development, inevitably involves apparently teleological, guiding patterns of organizing information. In addition, the biological entity, from conception to death, experiences its ontology (guided by inherent patterns of organizing information), as a perceiving being.

Perceptions are both shaped by the highest level of organization and registered as tacit, unconscious experiences that further reinforce the inherently existing pattern of organization. The development of the nervous system (sensorium) is precisely and innately ordered. While never fixed or inflexible, "sensorial organization emerges during development mediating an ever ordered, yet ever richer, more flexible, and more complex field of perception" (Laughlin 1983). In autopoietic terms this is the subordination of an organism's phenomenology to its structural ontology. In the same way sex is not a "thingness" given at some developmental stage and remaining an unchanged characteristic throughout life. Rather, sex is a verb, a process of a patterned organization of fundamental experiences. The shifting of sex as noun, to sex as a dynamic experiential process is fundamental to a more useful analysis of the foundations of gender. 


The cosmologies and belief systems of many cultures make non-arbitrary symbolic use of gender to label or make fundamentally distinct, components of experience or consciousness. By non-arbitrary we mean that the assignment of gender terms appears to be lawful and regularly patterned cross-culturally (Laughlin 1983). The basis of such patterned gender attribution may be rooted in a context of biogenetically structured perceptual experiences. The perceptual experiences are particular to each sex, with initial primary perceptions becoming layered upon with the subsequent unfolding of typical developmental processes. The primacy of perception over cognitive differentiation not only dominates early neurocognitive development but continues to form the 'ground of being' out of which cognition arises. The inherent order of perception is primary not only for moment-to-moment cognition but for ontogenesis as well (Laughlin 1983). The perceptual 'ground' becomes relatively unconscious as higher cognitive functions emerge and as such remains as a matrix of perceptual filters shaping the formation of a symbolic template.

In terms of autopoiesis what we are referring to is an equation of sex specific morphology and ontology with the structural (as opposed to organizational) aspect of an autopoietic system. Subsequently therefore, perceptual filters refer to the ontologically dependent phenomenology by which an autopoietic system specifies a reality (cognitive or otherwise).

To understand this sex specific phenomenology requires that at least two interrelated levels or orders of human sexual dimorphism have to be examined. The first level or order primarily pertains to species being, while the second level or order primarily pertains to individual being. Since the implications of the first level are pervasive throughout the second level, initial elaboration will begin with this level. It must be stressed that these levels are not mutually exclusive but are complexly interrelated. Furthermore, a complete elaboration of all the pertinent structural processes is impossible. What will be undertaken is a presentation of several interrelated lines of evidence by which we hope to establish the reasonableness of the thesis.

Instrumental to the formation of sex-specific perceptual filters and a symbolic template is the inevitable association of the womb with the lifeworld (Laughlin, 1983:2). Memories of the largely undifferentiated totality of immediate perceptual experience within the womb/lifeworld become associated with or symbolized by mother. Mother also becomes the first and quintessential 'woman'. Thus, despite the emergence of more advanced neurocognitive functions, a fundamental cognitive formula remains as an organizing or perceptual filter: "womb=woman=world" (Laughlin 1983). Although autopoiesis stresses the autonomy and self-referential circularity of living systems the cognitive equation cited above is not inconsistent with autopoiesis. The cognition of "womb=woman=world" can be likened to a first order (individual) autopoietic organism's perception of its autopoietic subservience to the higher order (species) autopoietic system.

The influence of the perceptual relationship of the pre- and perinatal child to the lifeworld is pertinent on at least two levels. Fundamental to sex-specific developmental processes and the corresponding organizing of perceptions are the different relationships of each sex to the maternal environment/lifeworld, or womb. On a cultural level, the predominating orientation toward the lifeworld will influence how the sex specific perceptual filters will specify and integrate particular cognitions of gender. For example, a positive orientation to the lifeworld tends to encourage individuals to substantiate, integrate, and potentially to transcend ontologically sex specific perceptual orientations into complementary cognitions of the other sex. By complementary we intend a sense of symmetry, balance and fluidity of interaction.

On the other hand, an ambivalent or negative orientation to the lifeworld fosters a substantiation, integration and crystallization of each sex into a cognition defined in terms of some sort of opposition to the other sex. By oppositional we mean a sense of a more radical asymmetry, conflict, segregation and anxiety emphasizing a need to control or dominate the other sex. Since the nervous systems of all people appear to develop in a very determinate manner during pre- and perinatal life, and the womb for all people provides a fairly similar environment we may feel secure in assuming that this sort of cognition process is universal (Laughlin 1983:245).

To reiterate, the developmental processes integral to each sex can be viewed as a tri-level experience: the unfolding process of the sensorium, the perceptual experience mediated by the sensorium, and the cognitive/cultural appreciation of the developmental process. While the underlying cognitive and perceptual processes are universal, the virtually unlimited potential for variety in behaviour arises with the highly complex interrelations between these levels of experience and the many other environmental and cultural variables that are possible.

An epistemology of gender presupposes the view that:

…consciousness is present in the prenatal child at or near conception and that it develops as function of the development of its operating neurocognitive structures, particularly those mediating the sensorium (Laughlin 1983:11).

Equating consciousness with symbolopoesis and the progressive development of the nervous system, assumes the subordination of an organism's phenomenology to its structure and ontology. To put it another way, each of these levels is guided by isomorphic patterns of organizing information. To understand the perceptually based knowing of gender that this work posits an appropriate description of the processual differences inherent to each sex is required.

It has been postulated that the X and Y chromosomes may be in charge of an auxiliary system which intervenes after conception in the way that the other 44 chromosomes are expressed (Durden-Smith and deSimone, 1983:113). It is believed that the X chromosome is largely sexually neutral. Its role in sex differentiation is primarily involved with the maintenance of the ovarian function in the female. Although the information it carries is essential for proper development beyond that specific to sex morphology, as no person, stillbirth, or abortus has been found without at least one X chromosome (Ounsted and Taylor, 1972:245,249). Even in the event where only one X chromosome is present, female morphological development proceeds to some degree with the exception that ovaries and the subsequent hormonal cycles do not develop.

Only the Y chromosome is sex determining yet does not contain any complex male forming genes. In fact it contains no significant genetic information specific to itself (only a gene for hairy ears) (Bleier, 1984:41). Its primary function is believed to be the "cause of certain potential autosomal and X coded, information to become manifest in the phenotype" (Ounsted and Taylor, 1972:245: see also Durden-Smith and deSimone, 1983:114). Furthermore, in males, the transcription of expressed genomic information takes place at a slower ontogenic pace (Ounsted and Taylor, 1972:245). The sexes differ in the regulation of their developmental pace, which when seen as a continuous and timely sequence of interactions between the expression of genetic information and environmental contingencies, implies important and widespread consequences for individuals of each sex (Ounsted and Taylor, 1972:246).

The first step in a long ontological sequence begins with the differentiation of the gonads early in fetal development. The differentiation of sex morphology occurs within the womb during the fifth to twelfth week of ontogenesis. For the first five weeks of embryonic life all embryos are morphologically female. If the fetal gonads are removed before differentiation takes place, the embryo will autonomously continue to develop into an apparent female morphology, lacking only ovaries, regardless of the genetic sex (Sherfey 1972:38). Sexual differentiation occurs during the following three to seven weeks. However, it is only the male who is required to undergo a sex-specific transformation of morphology (Sherfey 1972:40). In order to do this the male embryo must elaborate extremely large quantities of androgen (relatively speaking) throughout fetal life to overcome both its innate female anatomy and the effects of the circulating maternal estrogens (Sherfey 1972:43). Certain complications can arise if the particular male embryo happens for some reason to be androgen insensitive, or fails to produce androgen. In such cases the embryo will remain an apparently morphologically female, until puberty when expected further female development fails to occur.

At this point it is perhaps useful to characterize, on a sort of archetypal level, the male's perceptual experience of his relationship to the lifeworld that results from his structural developmental pattern. The male, to be and become a male,[8] must differentiate from some fundamental aspects of the World Matrix (as womb/lifeworld and represented by the maternal hormonal environment as well as by the initial female morphology). It is difficult to be more precise, for what is aimed at is a generalizable characterization of sex-specific structural transformations and the subsequent cognitions/phenomenologies associated with such transformative processes.

During the period of sex differentiation and in fact throughout the entire term the genetically female embryo's relationship (in terms of relatively sex-specific hormonal communication) to the lifeworld/environment can be characterized as one of similarity-to or identity-with. It is difficult to determine the significance of the role of either the fetal or maternal estrogen in the full development of the female pattern (Sherfey 1972:40). Of course it is acknowledged that the similarities of experience within the womb for all neonates regardless of sex, far outnumber the differences. Additionally, individual differences in experiences within the womb also outnumber those occurring between the sexes. However, the actual 'weight' of the differences may be substantially disproportionate to their number. The task of this work is the elegant characterization of the developmental differences particular to each sex. Thus, consistent with what could be likened as a type of higher level or archetypal pattern of organizational instruction guiding structural transformations, which in turn pattern perception and experience, the genetic male apparently has to differentiate from the environment (as womb=woman=world). Only in this way will the male be able to develop the expected male morphology and embark on the lifelong experiences corresponding with such a body. In autopoietic terms, this developmental pattern is more than a single structural transformation, rather it is a feature of the male's (as a living autopoietic system) ontologic organization, and thus of his organismic identity. We reiterate that maleness is not to be equated with masculinity. 

The female on the other hand can be characterized, in her pattern of morphological development, as identifying-with-the-environment[9]. The characterization is derived from the previously mentioned difficulty in determining the influential primacy of the fetal or maternal estrogens in the female neonate's development as well as the relatively homogeneous continuation of her ontology in respect to the initial morphology. Thus, the female's structural ontology may also reflect a particular organization/identity. This initial and embryonic genesis of sex morphology is the foundational perceptual template upon which later metamorphically similar perceptions will be overlaid/associated.

The next phase in the developmental sequence of patterned differences of perceptual experiences involves the interaction of infant and mother at birth. What is important to consider is not only the event of birth, but the entire period of early child development. Nancy Chodorow (1978) has elaborated the different perceptual experiences, from a psychoanalytic viewpoint, of pre-oedipal, and oedipal children. Chodorow feels that many, if not all, gender differences are due to the socialization occurring through the psychological experiences at this time. In particular, she believes that the differences in gender are the consequence of female-exclusive mothering. Her solution posits that early and equal involvement by males in the parenting of children would alleviate much of the gender-specific psychodynamics. Much as this may change many of the psychodynamics, it leaves the previously mentioned differences in ontological process and subsequent perceptual/cognitive experiences which are inherent in male and female morphology unaccounted for.

At birth a similarly patterned relationship to the mother/lifeworld is likely to occur, although it will be qualified by the particular culture's orientation to the lifeworld. The female child is born from a female and is female. A recognition which can typically arise on some level between the mother and daughter is (all things being equal) likely to embrace aspects of identity that build on the initial primary perceptual experience and organizational identity. The male child, however, is born from a female but is not female. A recognition between mother and son can typically involve some aspects of identity but would logically include a profoundly different emphasis on those aspects relating to the other-than-self[10]. Despite the fact that in some societies all children are categorized as 'its' along with the elderly, who also return to this category, the potential for the recognition of the individual child's future sex (if not gender) undoubtedly remains.

The different relationships to the lifeworld that are established in utero, during birth, and in early infancy continue to manifest throughout the life of the individual. Apart from the infant's bonding with mother as primary love object (Chodorow, 1978), the relationship between male and female parental figures is the first social dyad that is encountered by the infant. These parental figures not only represent the primary gender role models, but also provide the basis of family role interactions from which a child derives an initial orientation toward society (Laughlin, 1983:3).

Simultaneous with the growing awareness of the – parental male/female dyad is the gradual emergence of more advanced neurocognitive functions mediated by structures which include the prefrontal lobes, the inferior parietal lobe and secondary association areas. The cognitions which are mediated by these structures (and throughout their ontological unfolding) develop within an orientational context that is either in complementarity with, or in opposition to, the primacy of the world of immediate experience perceptually the womb=woman=world (Laughlin, 1983:4).

Despite the orientational context, cognitive development represents the differentiation of distinct concepts, objects and events from an undifferentiated unfolding-enfolding lifeworld. Furthermore, these cognitions emerge and develop in a sort of isomorphic conjunction with a growing awareness of the parental dyad and thus, become associated with the male parental figure and subsequently with the male in general (Laughlin, 1983:34).

Theoretical explanations of the equation of male with knowledge acquired during, and derived from, conceptual development would include the:

…recognition of simple intransivity (lifeworld = mother, mother father, father = cogito) in a Piagetian (1980:84) frame, or the simple logic of metaphoric and metonymic relations (lifeworld:mother :: cogito:father) in a Levi Straussian (1968) frame (Laughlin, 1983:4).

While the above equation utilizes the linking of mother with father, it may be important to note that the "institutions" of motherhood and fatherhood are quite different in that motherhood is incontrovertibly "organic" whereas fatherhood requires a more culturally dependent knowledge of paternity. This sort of knowledge is isomorphic with the neurocognitive process whereby the differentiation of discrete objects/events serves in the adaptation to an "ever unfolding-enfolding lifeworld" (Laughlin, 1983:4). Thus, despite the incredible cultural variation in the details of gender categories and roles, an initial non-arbitrary association of the female (and feminine gender categories) with the lifeworld, is matched by an equally non-arbitrary association of the male (and masculine gender categories) with the process by which cognition develops its adaptive structures (Laughlin, 1983:4). By extension it is equally possible that there is a non-arbitrary association of the male with a differentiation from the lifeworld.

The next significant phase in the unfolding ontology of sexual dimorphism which offers events and perceptual experiences with deep implications for each sex occurs at puberty. During this period of dynamic transition the morphologies and nervous systems of both sexes substantially mature, thus becoming (potentially at least) more actively engaged in higher order autopoietic (species level) phenomenology. The onset of this phase of development carries the potential for an increase in the cognitive appraisal of present and prior perceptual experiences. Experiences during this time are cognitive and perceptual, conscious and unconscious, unique to the period and patterned upon previous experiences. While many of the changes that both sexes undergo are similar in nature, some profound differences exist between the sexes, including the onset of menstruation in the female and possibly the mature phallus[11] in the male.  The significance of the menstrual cycle should be elaborated in order to grasp more completely the pervasive influence of the cycle in shaping perceptual experience, and substantiating the bio-symbolic template.

In much of the literature concerning the physiological features significant to the evolution of our species, the elaboration of the leap from the oestrus to the menstrual cycle has received little emphasis. The radical difference between oestrus and menstruation is often misunderstood. In the oestrus cycle sexual receptivity occurs only in conjunction with ovulation, and "bleeding" is both a visual and olfactory signal of approaching and actual receptivity. In the menstrual cycle, however, "the libido is liberated," as sexual receptivity is no longer dependent on ovulation in the female. Sexual receptivity becomes a question of a host of many other factors, which most likely increase as the psychological complexity of both the individual and the culture/environment increases. 

It is possible to view, for analytical purposes, the menstrual cycle as divided into four phases: pre-ovulatory; ovulatory; premenstrual; and menstrual. Consequently the complete rhythm of the cycle may be experienced as a fourfold one. However, these and other more complicated rhythms emerge from a basic and powerful twofold beat inherent in the two poles or culminations of the menstrual cycle: ovulation, the shedding of the ripe egg into the fallopian tube; and menstruation, the shedding of the thick, built-up lining of the womb resulting in the wall becoming thin and exquisitely sensitive and sometimes likened to a wound (Shuttle and Redgrove, 1978:29). 

Further characterizations can be made of the two poles to the menstrual cycle. Ovulation can be characterized as being concerned with the continuation of the species, embodying values pertinent to the survival of the species. Menstruation on the other hand can be characterized as being concerned with the individual female embodying values pertinent to individual survival (Shuttle and Redgrove 1978). Physiologically the two cycles, ovarian and uterine, are linked by very complex systems of nerve/hormone pathways interacting in networks of influence. The cycles are mutually sensitive, feeding back one with the other. Complicating matters, however, ovulation (with or without a temperature rise) may occur at any point in or even twice in the same cycle. Despite the possible regularity of ovulation at mid-cycle it remains sensitive to unknown rules. These unknown rules most likely involve phenomenological emergents[12] resulting from the unique human structural dimorphism in which both the biogrammatic (reproductive and non-reproductive) interests and capacities are brought into mutual relation and support. Thus, what is usually considered a single cycle under the label of the menstrual cycle can perhaps be more accurately analyzed as a bi-phasic cycle, representing an alteration of values oriented to the species at one end and the individual at the other.

Another common misapprehension concerning the menstrual cycle is its characterization as a larger period of normality punctuated by a shorter period of bleeding accompanied by unpleasant emotional and physical symptoms which in turn are assumed to be the basis of the development of menstrual taboos. However, the menstrual cycle is actually a continuous process of daily physiological and more often than not, unconscious psychological/attitudinal changes. Evidence of the largely unconscious attitudinal changes can be found in studies noting changes in the tone of sexuality and types of dreams experienced during the ovulatory or menstrual peaks (Shuttle and Redgrove 1978).

It is important to hold in mind the point made in the second chapter, that the menstrual cycle in liberating the libido makes possible a new level or order of the types of relationships and contingencies of relationship (emotional, economic, etc.). The possibility of new types of relationships is profound in its implication for the development of new types of social organization, and thus is a fundamental element in the foundation of any society. Further significance of the menstrual cycle can now be elaborated, so as to disclose the relation of this aspect of sex differentiation in the same vein as the account of pre- and perinatal development. 

It is not an uncommon phenomenon, that when a group (two or more) of women are in some form of close association their cycles can synchronize. The synchronization of the menstrual cycle that is possible between women can also extend to include the lunation cycle (Shuttle and Redgrove 1978:133-5,156-60). This sort of inter-subjective cycle synchronization can be a potentially profound source of "knowledge" of the world, potentially leading to the formation of information sharing and processing cults (religious or otherwise) (Shuttle and Redgrove, 1978:25). The cognitive and perceptual association of the female with the lunar rhythms and the moon, and the moon with the biosphere/lifeworld can act as a powerful reaffirmation of the original perceptual experiences of the prenatal relationship with the womb/world. Even though cycles do not always remain synchronized, or may not synchronize at all, it is tempting to make the association between the isomorphic nature of the lunar cycle and the average female cycle.

Riding on the end of a beam of light, we can examine the influence of the lunar cycle in the development of notions of time and thus also of certain types of knowing and memory. The lunar cycle provides not only a marker of the passing months, but with the new, first quarter (appearing as a half-circle), full, and third quarter (appearing as the other half-circle) moon, is a marker of the week. The lunar cycle also individuates each day within the context of a month as distinct from the other days. For the female, the lunar cycle thus provides a potentially external marker of her own internally experienced cyclic process. The resonance of experiences if the menstrual and lunar cycle are synchronized optimises the potential for the integration into the cognized environment of the notions of time, the body/psyche's internal processual cycling, and thus of certain types of knowing-predicting, or the beginning of a certain type of gnosis. The menstrual cycle's correlated phases of attitudes/orientation and dreams/symbols (Shuttle and Redgrove 1978) can also find their interpretive Rorschach in the daily transformation of lunar appearances. Thus, the physiological and psychological aspects of the menstrual cycle can find powerfully isomorphic parallels in the physical (e.g. tides and phasic appearances) and the symbolic (interpretive associations) aspects of the lunar cycle. The complex and multileveled possibilities of association between the menstrual and lunar cycle permits a greater security in the characterization of female development occurring in a metacontext of an identity-with-environment.

A parallel of the onset of menstruation in the female is the maturation of the male's experience of erection, and the capacity for ejaculation of a new fluid – semen. However, no matter how distinctly male this new capability is, it remains associated with the autoerotic, oceanic feeling, or uroboric experience of primal unity and thus with some aspect or guise of the maternal/feminine/natural (Neumann, 1954, see also Monick, 1987; Jung, CW 10; Vanggaard, 1972; and Dulaure, 1934). A brief elaboration of the phenomenological/cognitive dynamics involved with the male's "phallocentric" structural – ontological, transformations will help to delineate further the processual and organizational pattern that is relative to the male.

The symbolic aspect of the erect penis has commonly been termed "Phallus." As a symbol, its meanings generally extend beyond the directly biological[13] and the roles serving goals other than passion[14] or procreation (Vanggaard, 1972:11). In its symbolic aspect, the phallus is multivocalic"[15] and can incorporate implications of power, pleasure, fertility and more. All of these aspects overlap inextricably and as is generic to an understanding of any symbol, the comprehension of one aspect involves a simultaneous grasping of the symbol and its referents as a whole field.

The phallus as a symbol of power can be related to fundamental biogram patterns that have become utilized as tools communicating certain categories of contingencies of relationship. A prototypical demonstration of the aggressive erection is the baboon sitting on guard with an erect penis. Vanggaard (1972:109) suggests that since erections and seminal emission have been observed not infrequently in association with aggressive or fearful dream situations, aggressiveness may be an effective stimulus for erection or peno-anal activity. He goes further by comparing this sort of asexual erection occurring during dreams with the erections depicted in the bronze age petroglyphs:

...in the pictures of these rock carvings erection appears, as in dreams, in association with sexual and aggressive scenes and in addition with other activities such as sailing, plowing, and hunting which can be regarded as expressions of male powerfulness and capability in the widest sense, but which are neither directly sexual nor aggressive (Vanggaard, 1972:109).

Vanggaard's use of the terms "male powerfulness and capability" is perhaps misleading in that they tend to presuppose sex differences in capability and thus are likely to lead to the type of controversy founded on the confusion of sex differences with behavioral prescriptions. A more useful description of the association of the erection and the activities cited by Vanggaard may be in the isomorphic nature of the relational contingencies between the participant and the context. Thus rather than expressing inherent power or capability the erection as phallus is a symbol in a relational context. For example, the erection may be a response to a perceptual Gestalt of having to enter into (e.g. by "penetrating," "merging-with" or "being engulfed by") a relational context in which there is an implicit liminal experience to the differentiation of self from lifeworld.

While considerably more can be said that is of importance about the phallus, only one more feature is essential to consider in this discussion. The apparent autonomy of the phallus lends itself to a cognition of a type of transpersonal experience. According to Monick (1987:17):

…the physical phallus has become a religious and psychological symbol because it decides on its own, independent of its owner's ego decision, when and with whom it wants to spring into action. It is thus an appropriate metaphor for the unconscious itself, and specifically the male mode of the unconscious.

In Images and Symbols Mircea Eliade discusses this apparent "autonomous mode of cognition" as the basis of a transcendent means to knowledge. In fact he says that "sexuality has everywhere and always been a hierophany" (Eliade, 1969:14).

According to Neumann (1954:309):

…mythologically, the phallic-chthonic deities are companions of the Great Mother, not representatives of the specifically masculine. Psychologically this means that phallic masculinity is still conditioned by the body[16] and thus is under the rule of the Great Mother, whose instrument it remains.

There is much cross-cultural evidence indicating the perception of the autonomous nature of the phallus. For instance, Neumann (1954:49, see also Dulaure, 1934), states that all phallic cults, invariably solemnized by women, have the similar theme: the anonymous power of the fertilizing agent as the human individual is merely the bearer of "that which does not pass away and cannot be interchanged because it is the self-same phallus." The phallus as a symbol of fertility is like paternity, a cultural development. The male begins by "being a copulater, not a begetter." Even when the phallus is worshiped as an instrument of fertility it has generally been in the nature of the opener of the womb rather than the giver of seed and a bringer of joy rather than of fruitfulness (Neumann, 1954:309).

It is perhaps possible to understand the experience and symbolic cognition of the phallus as autonomous, in autopoietic terms. By considering the different levels or orders of autopoietic systems, then both the phallus and certain aspects of the menstrual cycle can be viewed as phenomenological consequences of the structural bridges between these different orders of autopoietic system (i.e. the bridge between the individual as an autopoietic system and the species as an autopoietic system). The subordination of lower order autopoietic systems to the maintenance of higher order autopoietic systems provides a firm base upon which the cognitive and perceptual phenomenology of sexuality as autonomous, transpersonal or hierophanic. While both males and female can experience their own sexualities as autopoietically hierophanic the difference between them is in the identification with the lifeworld (as higher order autopoietic matrix) which that sexuality serves.

Perhaps the most powerful indicator of the structural differences between the sexes can be found in the different experience/perceptions of each sex's involvement in procreation. The female in carrying the developing embryo has access to a cognitive and/or perceptual experience of "other" as within. Even more so, there are profound structural processes (autopoietic patterns of organizing information) which are required to make procreation possible. In accepting sperm and maintaining pregnancy the female has to modulate her own immune system. The immune system can be characterized as those aspects of an autopoietic system responsible for the maintenance of self/identity by discriminating against that which is not self. The female must be able to suppress one arm of her immune system so that it will tolerate the sperm and then the fetus inside her, while simultaneously boosting another arm in order to have the extra protection against infection she requires (Durden-Smith and deSimone, 1983:1745).

The autopoietic organization by which both the structural modulation of the female's immune system is guided and her ontological processes extend to include the maintenance of fetus and neonate can be elegantly characterized as multileveled identification with "other." These structural processes can generate a perceptual/cognitive phenomenology that is both isomorphic with and overlaid onto the previously characterized perceptions and cognitions. In this regard, it is clear that the male's structural ontology is radically different from the female's and thus likely to generate phenomenological cognitions relatively differentiated from the female's.

The final line of evidence which will be presented in support of this thesis concerns sex differences in brain structure. A good deal of research has been conducted on potential sex differences in brain structure producing few substantial results. For instance, sex differences in the nuclear size of nerve cells in the hypothalamus as well as sex hormone dependent differences in the way the nerve cells were wired, have been found (Durden-Smith and deSimone, 1983:117; Hutt, 1972:42). However, the research of central interest to this work has focused on sex differences in the lateralization of the brain. Briefly, there is evidence that the hemispheres of male brains are more specialized, communicating to each other in different languages – verbal and visual-spatial, and only formally after an encoding into abstract representations (Durden-Smith and deSimone, 1983:73; Ounsted and Taylor, 1972:138; Rossi, 1985:1824). On the other hand, the hemispheres of female brains appear not to be so specialized and thus able to communicate in a much less formal and structured way as well as more rapidly.

The caudal or posterior end of the corpus callosum (a bundle of fibers by which the two halves of the brain communicate with each other) has been found to be much wider and larger in women than in men. In fact:

…so big and clear was the difference that 'impartial observers' could immediately assign to the right sex – 'with 100% accuracy' – drawings made from photographs of cross sections (Durden-Smith and deSimone, 1983:76; see also Rossi, 1985:184).

These differences were also found in the brains of fetuses that were between the 26th and the 41st week of gestation. The difference in the sizes of this inter-hemispheric communicator suggests a greater ease and frequency of communication between the two hemispheres of female brains.

The implication of these sorts of structural (or neuro-gnostic) differences between female and male brains may be viewed as a framework that is homeomorphogenically related to the other structural differences which we have reviewed. That is, the male's greater hemispheric specialization and operational independence as well as the dedication of relatively fewer nerve fibers to inter-hemispheric communication can be viewed as both the outcome and mediating structure for the homeomorphogenically patterned perceptions/cognitions of a differentiation from the contextual matrix. The female's relatively greater correspondences and interdependence between hemispheres can be similarly viewed as a homeomorphogenetic outcome and related mediating structure of perceptions/cognitions of an identification with a contextual matrix. As was stated earlier an initial contextual matrix could be the pattern of the original female morphology as well as the perceptual association with the lifeworld.

This chapter has presented a theoretical base upon which an epistemology of gender can be placed. Various aspects of sex-specific structural ontologies have been outlined. The grounding of a cognitive system and phenomenology in the structural ontology of an autopoietic system was established in chapter one. Thus, despite the largely overriding similarities in the ontological development of all humans, the relative differences in the ontologies of the sexes has been posited as the base of correspondingly different cognitive systems. These different cognitive systems were characterized as different orientations relative to the lifeworld as a contextual matrix. The male structural orientation was characterized as a differentiation-from the lifeworld whereas the female structural orientation was characterized as an identification-with the lifeworld. The following chapter will further substantiate these two structurally based orientations through their application to some contemporary anthropological and psychological theories.

Chapter Four - Perceptual Orientation and the Specifying of a Reality


Thus far, a theory of the different autopoietic structures defining male and female morphology and ontology has been elaborated as a basis for what has been termed a symbolic template. By symbolic template is meant a kind of perceptual filter or archetypal pattern, by which information is organized or the phenomenology consequent on the different structures is patterned. However, the question of how such perceptual filters would shape a specific and culturally based symbolic template, or what a particular cognized environment specified by such a template would look like remains unanswered.

It is the aim of this chapter to elaborate a brief response to each of these questions. We will deal with each question in turn. While the scope of this work does not permit a complete and detailed elaboration, it is possible to illustrate some basic examples which I hope will provide the reader with a base to picture a more comprehensive complexity.

The work of Carol Gilligan (1982) provides a useful view of what a sex-specific cognized environment may look like. This work is particularly apt in that while it is contemporary, it presents the articulations of the "female voice" even when it has not been culturally heard and thus a retrospective hearing is possible. In the same vein it is possible that Gilligan's viewpoint may be used to describe universally these relatively sex-specific orientations. The second section of this chapter will explore the potential contribution of these two different orientations in understanding how different cultures develop specific sex-roles and relations.

∞            ⃝           ∞

In her researches in psychological and moral development Carol Gilligan (1982) has found different modes of thinking about relationship and has documented how these modes are associated with male and female cognized environments as portrayed in psychological and literary texts. One of the most significant barriers to hearing the different voices rests, in the theoretical frameworks presuming sexual neutrality and scientific objectivity while actually reflecting a consistent observational and evaluative bias which is specifically masculine. Thus the different voices (male and female) may be separated by an appearance of a common language. The recognition of such bias is possible with the acknowledgement that all categories of knowledge are human constructions (Gilligan, 1982:6). Gilligan, not only demonstrates that contemporary models of psychological and moral development are constructed with male observational and evaluative perspectives but also offers alternate models constructed with corresponding female perspectives.

Freud (1925:257-258) considered women as naturally less able than men to achieve a sense of the inexorable, impersonal and independent nature of justice. Recently, Chodorow (1978) attributed differences in what each sex considers ethically normal not to anatomy but to the universal responsibility that women largely hold for early child care. This responsibility has been postulated as the reason for the female's personality to essentially define itself more in terms of a relation and connection to others (Gilligan, 1982:7). As a result of this identification female identity formation tends to occur in a context of ongoing relationship since mothers and daughters have a greater tendency to experience themselves as alike and continuous with each other. Male identity on the other hand is more critically tied to separation and to entail a greater emphasis on individuation as ego boundaries are more defensively established (Gilligan, 1982:8). The foundation upon which Gilligan bases the developmental differences is consistent with the view, developed in the previous chapter, of a female perceptual orientation of an identity-with-environment/context and a male perceptual orientation of a differentiation-from-environment/context.

Gilligan (1982:9-10) cites evidence from a host of sources including both Janet Lever (1976) and Piaget (1970) indicating certain differences between boys and girls. For instance, boys increasingly become fascinated with the elaboration of rules and fair procedures for adjudicating conflicts. This orientation is felt to account for such behaviours as: boys tending to play more often in large and age-heterogeneous groups, and that their games tend to last longer than those of girls. Girls on the other hand, were found to not be so concerned with the elaboration and maintenance of such a legal system of rules. Thus, when a quarrel arose, the girls that were being studied tended to subordinate the game's continuation to the continuation of relationships between the participants. I imagine that while both girls and boys maintain systems of competition and rule making, the appearance, function, and nature of these corresponding systems would tend to differ in much the same way as has been outlined above.

In terms of competitiveness, Gilligan (1982:14-15) makes the point that the anxiety experienced by women in the "fear of success" is present only when one's success was at the expense of another's failure. Thus, as this view of individual achievement extends into adulthood, maturity can become equated with personal autonomy, and predominant concerns with relationship can appear as a weakness rather than as a strength. According to Gilligan (1982:17) the elaboration of the knowledge of intimacy, relationships and care is not only the centre of women's moral development, but also delineates a critical line of psychological development for both sexes.

When morality is conceived as concerned with the activities of care, then moral development involves the understanding of the primacy of responsibility, relationship and connection. However, the conception of morality as fairness leads moral development to emphasize the primacy of the individual and of separation as well as an understanding of rights and rules. In this view moral problems arise for women due to conflicting responsibilities rather than because of competing rights. Resolutions for each type of moral problem requires a corresponding mode of thinking – contextual and narrative for the first and formal and abstract for the second (Gilligan, 1982:19). Consequently:

It becomes clear why a morality of rights and non-interference may appear frightening to women in its potential justification of indifference and unconcern. At the same time, it becomes clear why, from a male perspective, a morality of responsibility appears inconclusive and diffuse, given its insistent contextual relativism (Gilligan, 1982:22).

The two orientations toward morality not only speak of the differences between the sexes but also provide alternative conceptions of maturity. A brief example may serve to illustrate more clearly these two orientations toward moral problems. Gilligan records the responses of a typical boy and girl when posed with a classic moral dilemma. The dilemma concerns a man whose wife will die unless she receives a certain drug. However, the husband has no money to buy the drug. What should he do?

Typically the boy sees the conflict as one between life and property that can be resolved with a logic of justification. By choosing theft of the drug the boy avoids confrontation and abstracts the moral problem from an interpersonal situation. Using a logic of fairness in order to cast it as an impersonal conflict of claims the boy transposes a hierarchy of power into a hierarchy of values (Gilligan, 1982:32). The girl on the other hand appears initially to hesitate, somewhat bewildered. While theft does not seem a proper solution, what is incomprehensible to her is that the druggist and the husband do not come to terms. Her solution lies in activating the network of relationships by communication and including the wife by strengthening rather than severing the connection. This shift changes the moral problem from unfair domination and imposition of property over life into the unnecessary exclusion of the wife by the druggist's failure to respond to her (Gilligan, 1982:32). Thus the boy demonstrates a sophisticated understanding of the logic of justification whereas the girl reveals an understanding of the nature of choice that is equally sophisticated (Gilligan, 1982:32).

The contrasted images of hierarchy and network within the two different views about morality illustrate complementary perspectives. The girl assumes connection and can begin to explore parameters of separation, while the boy assuming separation can move to explore connection. Subsequent developmental paths would differ correspondingly for the male and female. The male's development would entail the realization that other is equal to the self and through that realization comes the provision that connection is safe. For the female, development proceeds from the inclusion of herself within an expanding connective network and the understanding that separation can be protective rather than only isolating (Gilligan, 1982:39). By understanding these two different developmental paths delineated as they are by differences in the way the perceptual experiences of separation and connection are aligned with the "voice of the self" it is clear that the representation of the male's development as the only model of development creates a ubiquitous problem in interpreting female development (Gilligan, 1982:39).

Other evidence cited by Gilligan included the findings that in thematic apperception tests men tended to project more violence into situations of personal affiliation than they projected into impersonal situations of achievement. Women, in contrast perceived more violence in the impersonal situations of achievement than they saw in the situation of affiliation (Gilligan, 1982:41).

In the same vein, Robert May (1980:59-71) identified corresponding patterns in the fantasies of men and women. The male pattern, termed by May as "Pride" leads from enhancement to deprivation, from an initial experience of separation (the severance of connection) to an irreparable loss, from a glorious achievement to a disastrous fall. Here the theme is one of life as a succession of relationships, of replacements and separations with attachment or connection as the final reward of this dangerous and elusive quest.

The female pattern which May names as "Caring" tends to be a narrative in which connection although leading through separation is ultimately maintained or restored. Within a thematic context of life as a web, and a process of continuity and change in configuration, women portray autonomy as the illusory and dangerous quest (Gilligan, 1981:48).

In the analysis of men's and women's self-descriptions Gilligan found the same orientation of identity around the themes of separation and attachment. Even highly successful and achieving women depicted their identity ("future mother," "present wife," "adopted child," etc.) and measured their strengths ("giving to," "helping out," "not hurting," etc.) in relational terms (Gilligan, 1982:159). In the self-description of men, involvement with others is related as a qualification rather than a realization of identity. The verbs of attachment that were used by the women are replaced by the men with adjectives that are descriptive of a singularity distinct from others. Thus the men describe themselves as "intelligent," "logical," "honest" and even of having or wishing to have "real contacts" or "deep feelings," although no particular person or relationship is mentioned (Gilligan, 1982:160-1).

It is possible to see how such different vantage points entail different critical experiences in the developmental paths of each sex. Despite the fact that the nature of the dilemmas inherent in such critical experiences may be the same for both sexes – for instance, a conflict between integrity and care – each sex is likely to approach the developmental transitions with a different perspective. For males, intimacy will in all probability be a primary transformative experience in the transition from adolescence to adulthood. For women, the parallel is not intimacy but the experience of choice that creates an encounter with self through which the understanding of responsibility and truth becomes clarified (Gilligan, 1982:164). Perhaps the most important point that Gilligan makes concerns the possibility and necessity of alternate models of moral and psychological development. Rather than presupposing a universal model of psychological development based on hierarchical stages of separation and individuation (for example see Levinson, 1978; or Mahler, Pine and Bergman, 1975) it may be more appropriate to frame an additional model based on stages of increasing complexity or extension in the web-like nature of responsibility and relationship. For example, it is possible to conceive of the development of identity as a process of incorporation. In such a view, a particular ego/identity develops through stages of the incorporation of the cognized environment. In this way, the increasing differentiation of the lifeworld (as cognized environment) reflects the increasing differentiation of the ego/identity as a complex whole consisting of many "parts." 

Gilligan's elaboration of two perceptual orientations contextualizing moral and developmental knowledge can be eloquently summarized in the following statement:

... men and women may speak different languages that they assume are the same, using similar words to encode disparate experiences of self and social relationships. Because these languages share an overlapping moral vocabulary, they contain a propensity for systematic mistranslation, creating misunderstandings which impede communication and limit the potential for cooperation and care in relationships. ... however, these languages articulate with one another in critical ways. Just as the language of responsibilities provides a web-like imagery of relationships to replace a hierarchical ordering that dissolves with the coming of equality, so the language of rights underlines the importance of including in the network of care not only the other but also the self (Gilligan, 1982:173).

Gilligan's work presents a clear depiction of a structurally based phenomenology as it is shaped within a particular culture. The two voices which Gilligan presents are isomorphic with the perceptual orientations elaborated in our thesis. That is, the male's perceptual orientation toward a differentiation-from-environment/context is consistent with Gilligan's hearing of the male voice as one of abstraction, separation and individuation. In the same way the female's perceptual orientation toward identification-with-environment/context is consistent with a female voice that is narrative, contextual and centered on care and responsibility.

However, Gilligan posits a neo-Freudian theoretical foundation (Chodorow, 1978) upon which to base the differences in perceptual orientation and subsequent "language." This theoretical foundation is not only consistent with but is encompassed by the thesis elaborated in the previous chapter. We agree with Chodorow's description of the psychodynamics between primary caregivers and infants, and the subsequent necessity to involve males in early child care. However, the understanding of different perceptual orientations recognizes that the differences in the experiences of males and females are founded on the structural and ontologic differences between them.

The perceptual and cognitive orientation of the male can be represented in the equation: differentiation-from-environment/context=separation=individuation.

This equation is in turn congruent with the formula stated previously:
mother = lifeworld, mother father, father = cogito.

The complementary perceptual and cognitive orientation of the female can be represented with the equation:
connection = identity-with-environment/context = lifeworld =  responsibility/choice. 

∞            ⃝           ∞

This section will offer a very brief theoretical exploration of some ecological metaphors consisting of some of the possible interaction of particular environments and the previously elaborated sex-specific perceptual orientations in the development of egalitarian or non-egalitarian relations between the sexes. A much greater degree of complexity is involved in an adequate elaboration of the emergence and development of any type of social relationship between the sexes. However, despite the limitations in the scope of this section, the potential explanatory usefulness of the perspective being developed here may be seen with some simple illustrations. At minimum we hope these few illustrations will permit the reader to glimpse the larger panoramic scheme.

The cognitive structures (whether complex or simple) responsible for the establishment of culturally specific sex-relations can be summarized as:

…a product of neurobiological structures and processes that obtain at a deeper level in the organism's biogram, on the one hand, and a product of the range and intensity of environmental stimuli that are perceived as significant by the organism, on the other hand (Laughlin, and Brady, 1978:2).

The important point to take note of is the perceptual orientation specific to each sex in the determination of what is considered significant. Furthermore, the positions of the actors within a particular social infrastructure are generally predicated on some sort of combination of factors influencing the rights of access to basic resources, and based on the shared physical, cognitive and social space. While functional integration of these positions is promoted by the sexual division of labour, the demands of incest taboos and exogamy as well as the obligations involved in exchange relations, the scope and intensity of such positions can vary in response to a host of environmental and cultural influences. Additionally the positions of these actors are subject to changes over time as information pools and contributions also change (Laughlin and Brady, 1978:11).

To put it more simply, we can posit that certain environments (and social organizations and demographics made possible therein) may tend to favour or require for the survival and welfare of the inhabitants, particular categories of activities. Such activities may in turn be relationally isomorphic with one or the other of the sex-centered perceptual orientations outlined previously. In this way the subsequent cognized environment may seem naturally to order egalitarian or non-egalitarian relationships between the sexes. By egalitarian we mean a type of inter-dependence and balance, a sort of sexual symmetry or integration. By non-egalitarian we mean a more radical asymmetry and segregation in the relational roles between the sexes (Sanday, 1981:170-1).

Sanday (1981:33) has found that a significant predictor of sex-role behaviour within a particular culture is the creation symbolism represented within its origin myth. Despite diversity of content three consistent themes are regularly present in creation stories:
  • A description of a creative agent;
  • An implicit or explicit designation of the agent's origin; and
  • An account of the agent's method of creation (Sanday, 1981:57).  
Creation stories reflect a cultural perception of the sources of power in terms of what Sanday names "inner" or "outer orientation." Sanday (1981:57) identifies three categories of creative agents:
  • Female creators, generally originating from within something (i.e. water or earth) and create from their own bodies;
  • Male, animal and supreme being creators who originate from without (i.e. the sky or another land) and create magically; and
  • Couple creators originating from both within and without, and tend to create by natural reproductive processes.
Therefore, in creation stories, the female is associated with nature, natural processes and an inner orientation toward sources of power. The male on the other hand is associated with the sky, magical processes and an outer orientation toward sources of power (Sanday, 1981:58). These associations are consistent with the characterization of male and female processes that have already been outlined in the previous chapter. That is, the female's perceptual orientation toward an identity-with-environment /context is consistent with an inner orientation toward sources of power, whereas the male's perceptual orientation toward a differentiation-from-environment/context is consistent with an outer orientation toward sources of power.

The orientation of a particular culture around particular creation symbolisms can be traced to the way the people interact with their environment (Sanday, 1981:65). Both the nature of the environment and the types of activity patterns necessary to maintain the economic infrastructure are key influences in the genesis of origin mythology. The workings of these influences are perhaps most evident in non-industrial societies where the people are closer to the complex web of natural phenomena.

For instance, Sanday (1981:68) posits that if the environment is predominantly a source of danger (i.e. in the form of large animals) inducing a relative sense of vulnerability, then an outer or animal orientation (measurable in such terms as the distance of males from infants and in beliefs about outer power) is likely to occur with a subsequent male origin symbolism. On the other hand, if the environment is perceived as beneficent, its lushness providing a sense of security and food is derived from the earth, then there is likely to be an inner orientation (measurable in terms such as greater male involvement with the young and beliefs about inward power) and a subsequent female origin symbolism (Sanday, 1981:68).

Sanday's conceptions of outer and inner orientations are consistent with the sex-specific perceptual orientations elaborated in chapter three. For example, a hostile environment is more likely to put a greater emphasis on the adaptive cognitive functions of compartmentalization, replacement, and hierarchical social structuring (Laughlin and Brady, 1978). These cognitive patterns tend to be more isomorphic with the male processes underlying the perceptual orientation characterized as "differentiating-from-context" in the previous chapter.

Accordingly, the relations between the sexes are less likely to be egalitarian. That is, through the cognitive formula of Womb=Women=World and the perceptual identification of the female with the environment, the relationship of the culture with the environment presents perceptual and cognitive parameters for an isomorphic relationship between the sexes. Thus, if the environment is perceived as dangerous, then by association females are more likely to be considered as dangerous by males. An evoked desire for the control or domination of the environment is likely to evoke an isomorphic desire by males to control or dominate females.

Migration as well as technological complexity, also tend to favour sex relations that are non-egalitarian as the underlying perceptual associations would be much the same. However, if a culture maintains female creation/origin symbolism then it is more likely to resist a shift from egalitarian relations between the sexes. The metaphors inherent in the female creation symbolism provide a basis upon which to organize the cognitive environment during social disruption (Sanday, 1981:133).

Cultures with a long and stable association with one environment tend to have egalitarian relations between the sexes. In these cultures, as in the majority of foraging and fishing societies, women tend to wield secular as well as religious power and economic and political authority. In such conditions there is likely to be an inner orientation toward the perceived sources of power (Sanday, 1981:5). The perceptual or cognitive associations of the environment, with an "inner orientation," and the defining female processes described in Chapter Three as "identity-with-environment" are likely to establish relationships between males and females that are isomorphic with the relationship between the culture and the environment. In this way the interdependence and balance of the relational positions between the sexes act out the interdependence and balance of the relationship between the culture and environment.

While a comprehensive elaboration of the dynamic interplay between the perceptual/cognitive orientations and cultural, environmental, interpersonal variables would require its own volume. We hope the brief sketch outlined above is sufficient to provide an understanding of explanatory usefulness of the theoretical perspective developed within this work.

Chapter Five – Conclusions and Implications

In Chapter One we stated that the purpose of this study was an elaboration of a useful theoretical frame within which the study of some aspects of sex differences and similarities, as well as the social construction of gender, can be carried out. The present controversy concerning the nature of the possible differences between the sexes has generally been conceived in dualistic terms. Chief among the many polarized conceptualizations of this controversy is the contemporary emphasis on the social construction of gender in opposition to (and reaction against) notions of biological determination. While this emphasis is not misplaced in relation to the analysis of gender categories, it does tend to obfuscate the complex involvement of the biology of sex dimorphism as the basic parameters by which genders are socially constructed. Thus, the problem centers on an understanding of how the biological referents of the differences between the sexes can be acknowledged as a foundation upon which gender is socially constructed while at the same time not as a foundation upon which absolute behavioral prescriptions can be made. The thesis developed in this study was argued to present a theoretical solution to this sort of controversy by unifying both the dimensions of biological processes and social constructions within a single view.

The first step in the elaboration was an outlining of some of the problems within the present epistemological and language frameworks. A summary of the theory of autopoiesis was offered primarily as a powerful epistemological framework able to explore at many levels (i.e. cellular, organismic, or species), the link between biological structure and ontology and a consequential phenomenology. Autopoietic theory was considered a particularly apt framework for an understanding of both the differences between the sexes as experienced at an individual level or of the interaction of the sexes as components of a single species. This thesis posited sex-specific differences in perceptual orientation, based on some structurally and ontologically different processes and the associated phenomenology.


In Chapter Two an evolutionary context was articulated. This context allowed us to frame some relevant parameters of the human biogram in terms of some of the unique systems serving the sexual dimorphism inherent in this species. Also elaborated were some of the implications experienced by individual (regardless of sex), of this particular species serving dimorphism.

Chapter Three presented an outline of some of the structural and ontological processes unique to each sex. It was hypothesized that the processes corresponding to many of the sex-specific developmental (structural and ontological) transitions were patterned on a relatively isomorphic basis. That is, as a meta-level pattern of organizing information guiding structural and ontological development and simultaneous perceptually experienced.

The female developmental process was characterized by a consequent perceptual orientation of an identification-with-environment/context.

The male developmental process on the other hand was characterized by a consequent perceptual orientation of a differentiation-from-environment/context.

In Chapter Four, evidence supporting the existence of these sex-specific perceptual orientations was presented through the work of Carol Gilligan (1982). Gilligan's findings, concerning the need for two models of moral and psychological development corresponding to each sex, were briefly summarized and integrated into the theoretical framework of this thesis. Males were found to approach moral problems in terms of an ethic of individual rights, autonomy and non-interference stressing a formal and abstract mode of thinking. Females tended to approach moral problems in terms of an ethic of responsibility, relationship and care stressing a narrative and contextual mode of thinking.

Correspondingly the model of psychological development positing hierarchical stages of separation and individuation was found more accurately to describe male developmental experience. Gilligan suggested an alternative model of psychological development framed in terms of stages of increasing complexity or extension in the awareness of the web-like nature of responsibility and relationship.

The chapter concluded with a brief analysis of a few of the possible interaction between the sex-specific perceptual orientations and certain environmental contingencies. It was posited that: (1) these perceptual orientations were the basis for a gendered descriptive and symbolic language used to render the world recognizable; (2) in turn the recognition of the environment would be instrumental in the formulation of culturally specific egalitarian or non-egalitarian relations between the sexes.

The study has had to confront a number of limitations. Chief among these limitations has been in the nature of available time and space. Subsequently, there is a considerable amount and scope of material that was not able to be covered. We have not dealt with a vast quantity of literature concerning some of the traditionally researched sex differences in behavior. For example, differences in speech or visual-spatial ability, aggression, passivity etc.. Additionally, we have not examined overt or covert sexuality or sexual behavior, except to make the point that sexuality is an individual expression of the complex relationship between personal, familial and cultural experiences and one's sex. Also not dealt with were the substantial proportions of similarities between the sexes. Neither have we dealt with the structural and ontologic transformations occurring in later life.

However, on the basis of the lines of evidence presented we can conclude that there are inherent sex-specific perceptual orientations arising out of different male and female structural and ontological processes and their associated phenomenology. We can also conclude that sex-specific perceptual orientations are influential in the recognition of environmental contingencies and in this way contribute in the formulation of culturally specific relations between the sexes. Thus, we are able to accept and refine the definition of gender offered in Chapter One.

Thus from two sexes are born the potential for multiple gender categories and innumerable sexualities or varieties of sexual behaviour. Genders emerge as socially constructed categories consisting of combinations of components of behavior perceived as isomorphic or at least consistent with the sex-specific perceptual orientations. Within this definition lies the substance of an epistemology of gender.

The concept of differences in the perceptual orientation of each sex is capable of making some significant contributions to the explanation of many of the observed differences in the expectations and roles occurring between the sexes. However, it must be stressed that these different perceptual orientations provide no basis for the prescription of roles or behavior.

The overwhelming similarities between humans, including a complex behavioral and neuro-structural architecture (biogram) which integrates reproductive and non-reproductive phase specific systems, provides substantial ground for asserting the generalization that every individual member of the species has access to the whole behavioral repertoire of the species. By stressing the primacy of perception as a basis for fundamental differences between the sexes we are able to acknowledge the influence of biological processes in shaping initial and inherent perceptual orientation. However, potential behavioral capabilities cannot be determined or prescribed since identical behaviors can be produced by a variety of different structural and organizational processes.

The implications of sex-specific perceptual orientations based on correspondingly different structural and ontological processes are numerous, multi-leveled and far-reaching. The sex-specific perceptual orientations are fundamental components out of which culturally created symbolic templates arise. Conceived in this way, these perceptual orientations can become powerful analytic tools to further the understanding of the dynamics behind a spectrum of cross-cultural and trans-cultural phenomena. For example, a cross-cultural re-examination of the rites of passage and initiation of both sexes from a perspective of the epistemology of gender elaborated here contribute to an understanding of their psychological importance.

The importance of such rites may lie in their provision of appropriate psychic, affective and symbolic contexts for the cognitive integration of the unfolding perceptual experiences inherent in the phenomenology associated with individual structural and ontological development. The timing of appropriate cultural events with the sex-specific ontology may facilitate the individual to orient toward the "self," the "other" and the cultural context. Thus, an important implication of sex-specific perceptual orientations lies in their potential to contribute to a foundation upon which to organize educational and personal development. For example, the optimization of the flexibility of one's cognized environment can be facilitated through the utilization of the concept (and techniques therein) of a "symbolic penetration" (Webber, 1980) in relation to the perceptual orientation embodied in one's own and the other sex.

The comprehension of the sex-specific perceptual orientations and subsequent epistemology of gender potentially provides a base from which the facilitation of greater intra- and inter-sex communication and understanding can take place. An ability to acknowledge sex differences that are not prescriptive of behavioral capabilities can facilitate the "tuning into" the voice and language differences inherent in different perceptual orientations. In this way, the sexes are less likely to become "separated by a common language."

The use of these sex-specific perceptual orientations to examine and analyse the tremendous variety of sexual behavior, both within our own culture as well as cross-culturally, may prove extremely useful. "Sexuality," which can be considered as related to but distinct from "sexual behavior," may also be subjected to useful analysis with the use of the perceptual orientations. Despite varieties of sexual preference there may be similar perceptual/cognitive dynamics involved in the evocation of arousal states. An enumeration of all the potential implication of sex-specific perceptual orientations is not possible but it is appropriate to outline some areas of further research.

Besides the research required to explore the implications already stated, a more comprehensive and exhaustive elaboration of the sex-specific structural and ontological processes is necessary. Equally important is a more detailed elaboration of the dynamic interactions between the structural and ontologic processes and the web of environmental contingencies. Both elaborations will assist in establishing the complex network of specific processes influencing the organization of a gendered cognized environment. Important to include in future research is the potential contribution of this epistemology of gender towards: 1) the delineation of individual sexuality, and 2) the situating of those individuals who stand out as exceptions (physiologically and psychologically) to "normal" male and female development.




[1]The use of the term "polymorphous pleasure" is an obvious derivative of Freud's well known descriptive phrase for infant sexuality, "polymorphous perversity". I intentionally use the word pleasure rather than perversity to shift the framing of sexuality to a more positive light and to avoid the assumption that human nature is somehow innately predisposed to the pursuit of "uncivilized" sensations. Furthermore the emphasis of pleasure allows the assumption that the many forms that sexuality can take are at some level motivated by an experience of pleasure, which in turn places the functioning of sexuality more on the level of the individual rather than on the level of the species. 

[2]This remains true of the instinctual aims and objects on the psychological (the phenomenology emerging from the organisms structure) level as well.

[3]The ability to communicate and think in terms of negatives, for instance, communicating what is not occurring "This is not a game" or what is not desired "I don't want the chocolate cake", is perhaps uniquely human (Bateson, 1972).

[4]Symbolopoesis and phasia are the prerequisites to the capacity to communicate in terms of negatives which as previously mentioned may be a uniquely human process.

[5]The ubiquity of contingencies of relationship, as a "communicational or representational unit" is evident even in the contractual nature of our concept of justice. The "contract" provides a "security" or stability to the relationship of an individual to a group, a society, another individual, etc.

[6]Indeed although, the distinction between oestrus and menstrual cycle has been made, the elaboration and implications of the differences between these two types of reproductive cycles is strangely missing from a great deal of the literature. 

[7]Count speaks of this concept in terms of the survival of ingredients from the mass of behaviour that was mobilized around the lactation process. However, it remains a useful descriptive term for the sequential or simultaneous incompatibility of multiple statuses in one individual while transacting with another individual also holding multiple statuses.

[8]By male is intended a biological integrity in morphology and not any psycho-social aspect associated with that particular body. Throughout this work maleness is not to be equated with masculinity.

[9]The choice of the descriptive terms "identifying-with-environment" and "differentiation-from-environment" are admittedly evocative at the least. However, in considering the great amount of controversy surrounding the subject of sex and gender the terms do permit an adequate descriptive power while not euphemistically evaporating the potency of the controversy. 

[10]This may likely to be more pertinent to the mother's experience than to the infant's. Some of the structural and organizational implications for the mother will be examined later.

[11]A great deal of controversy exists over the use and meanings of the terms penis and phallus. The term phallus has been chosen here as it more adequately represents the multivalent and transpersonal functioning of the systemic structures involved and consequent phenomenology therein. While penis may be descriptive of an anatomical and personal organ, Phallus seems a better term for the functioning and impersonal "being" evident in the not uncommon attribution of pet names such as "Mr. Happy" or "The Wonder Weasel" (Robbin Williams, various movies).

[12]For instance there is evidence that the particular interaction between an individual female and her ideological orientation toward either or both of the poles of her menstrual cycle may influence the onset and type of PMS suffered (Shuttle and Redgrove, 1978:40). Other evidence indicates that both the orientation of the female's sexual initiative and the thematic nature of her dreams experience a cyclic shifting in conjunction with her menstrual cycle (Shuttle and Redgrove, 1978:101). 

[13]The term biological should be understood in this instance in a very narrow sense. It is presumed that by biological is implied an orientation opposing the body with the mind. A more useful analytical concept can be found in the autopoietic notion of structure. In this way the symbolic/phenomenological emergents can be more easily associated and integrated with structural and ontologic transformations.

[14]It is perhaps inappropriate to discount passion per se, from the roles that are served. It may be that to the author, the term passion is used to indicate a conception of the affections involved with sexuality. If so, the phenomenology resultant from the interaction of the male's individual structural functioning and the structural functioning involved with the higher order of autopoietic organization of which the male is only one component, may be the source of the so called passion. Subsequently, passion should be considered much more complex and integrally involved in the meanings and goals served by the phallus. For a more complete elaboration of "passion" see Johnson, 1983.

[15]This is a term used by Victor Turner (1967:5052). 

[16]It must be kept in mind that the Jungian understanding of the body expressed here is somewhat different than the understanding being developed in this work. The body in Neumann's sense is associated with matter and thus with nature and the lifeworld. This view is essentially valid and is not inconsistent with the view being developed in this work.




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