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From biology to desire and action

How biological state becomes experienced value, motivation, decisions, reasons and interaction.

BERM treats the formation of motivation as part of the biological chain. Hormonal and neural state help determine what attracts attention, feels rewarding and seems worth the effort. Deliberation operates on those experienced values. The model therefore explains both what people are able to do and what they want, choose and give reasons for doing.

What enters this level

The receiving, endocrine and neural state described in Biology: hormone responsiveness, timing, energy, redox and electrical function. Their EMF-related change enters through the physical receiving bridge.

What carries forward

A distribution of initiatives, responses, choices and repeated actions. Interaction turns these individual outputs into relationships, population outcomes and the renewal of institutions.

State and experienced value

Changing biological state can change the weighting of reward and effort, and willingness to act, without a corresponding loss of ability.

An action has a possible benefit, a likelihood of success, an effort cost and consequences for oneself and others. The external situation supplies some of these quantities; biological state contributes to their experienced weight. A person can still perform a task while becoming less willing to choose it. Conversely, a particular immediate reward can become more compelling while sustained effort becomes less attractive.

Measured connections

Westbrook combined dopamine synthesis imaging and drug interventions in cognitive-effort choices; effects depended on baseline synthesis capacity. Jurgelis manipulated sleep in 24 participants and found greater aversion to cognitive effort while the short physical-effort comparison did not change in the same way. Draper’s randomized inflammatory challenge reduced acceptance of high-effort options without a corresponding significant change in reward sensitivity. Westbrook 2020i; Jurgelis 2022i; Draper 2018i.

What BERM draws from this

BERM explains changes in experienced priorities through measurable biological states. The same amount of time, money or effort can acquire a different weight. Stated lack of resources can therefore combine a real constraint with altered valuation. The parsimonious target is the joint pattern across choices, using shared state variables and task-specific consequences.

Desire, attachment and care

Biological regulation of the reproductive axis participates in sexual motivation and neural processing of sexual stimuli.

Motivation to approach, readiness to respond, sexual arousal, attachment, wanting a child and caring for another organism are related outputs with different functions. Reproduction requires both opportunity and functional transitions. BERM accordingly includes the biological formation of initiative and responsiveness alongside the capacity to conceive and maintain a pregnancy.

Measured connections

Finkelstein’s gonadal-suppression and hormone-replacement experiments separated testosterone and estradiol contributions to male sexual function. In Mills’s crossover trial, 32 men with low sexual desire completed both kisspeptin and placebo conditions; sexual-stimulus brain responses and penile tumescence changed without a significant measured testosterone change. The maximum tumescence increase was a physiological measure, not a percentage increase in desire. Finkelstein 2013i; Mills 2023i.

What BERM draws from this

The reproductive pathway has two coupled branches: whether an attempt occurs, and whether it succeeds. A biological shift can reach both. Desire for a child and a concrete attempt need their own observations and transition rules; the model can then explain how motivation, partner response, age and physiological capacity combine over time.

Reproductive regulation · behaviour · feedback

From felt motivation to realised reproduction

Animal interventions show selective changes in reproductive interest; human hormone interventions locate sexual responses and target-specific endocrine gates. BERM follows desire into approach, the other person’s response and an actual encounter. The biological success of that encounter remains a separate branch, alongside caregiving and its feedback.

Peragine et al. (2017)iMills et al. (2023)i
Follow the three branches and their evidence

Calcium · redox · hormone production

Production capacity continues into motivation and action

Autophagy links cellular maintenance to cholesterol availability and steroid production, including in human ovarian and testicular tissue. A randomized testosterone trial in older men with low testosterone and low desire connects hormone intervention to sexual activity and desire.

BERM carries hormone production through tissue response, motivation, opportunities and reproductive function. The trial’s age and hormone context stay attached to its finding.

Esmaeilian et al. (2023)iCunningham et al. (2016)i
Explore the shared mechanism and its studies

Time and learning

Biological state changes feedback-learning weights and choice consistency, so a transient state can influence later action through learning.

The organism’s state affects the choice made today and the history from which tomorrow’s choices are learned. A reward, failure or social encounter can update expectations with a different weight under different states. Learned routines and changed opportunities can then carry an effect beyond the initial physiological episode.

Measured connections

Lim compared a week of restricted sleep with a rested condition and found altered positive-feedback learning and more stochastic choices despite similar overall accuracy. Westbrook’s later dopamine study connects biological intervention to learning and effort-related choice within the broader RADBOUD-DA research program. Its 2020 and 2025 publications provide connected outcomes, not automatically independent replications. Lim 2026i; Westbrook 2025i.

What BERM draws from this

BERM carries state into the learning operator. The later persistence of a behavioral pattern can reside in learned values, a missed encounter or a changed relationship. An acute hormone change does not have to remain physically unchanged for years to have a lasting consequence.

Lt+1=U(Lt,feedback;St)L_{t+1}=\mathcal U(L_t,\mathrm{feedback};S_t)

L is the accumulated learning state, feedback is the experienced outcome and S is the biological state during updating. The equation specifies a model connection; its parameters are estimated for the actual task and data.

Decisions and reasons

An expressed reason is an observation of the decision process and can also be produced for an unnoticed change of choice outcome; it does not by itself identify motivation’s causal origin.

A person reasons from what appears desirable, feasible, threatening or costly. If biology changes those weights, a coherent explanation can change with them. The experienced reason is itself part of the event to explain. BERM therefore follows state into valuation, deliberation, action and the account a person gives of that action.

Measured connections

Johansson covertly changed the outcome of a face choice; participants sometimes justified the substituted outcome without detecting the mismatch. Eisenegger randomized testosterone administration and measured participants’ later beliefs about the administered substance. Drug assignment and reported belief showed different associations with offers; only drug assignment was randomized. Johansson 2005i; Eisenegger 2010i.

What BERM draws from this

An articulate explanation is not automatically an independent upstream cause. It can express a biologically shifted motivation and can subsequently become a remembered commitment or guide for action. Deliberation and learning remain functions of the biological system. This structure does not require every reason to be post hoc or every external constraint to be imagined.

Measured connections

Crockett’s two randomized drug experiments changed how money was weighed against pain to oneself or another person: serotonergic and dopaminergic interventions produced different patterns. Strang’s randomized crossover breakfast study changed costly rejection of unfair offers. Tyrosine was a measured candidate mediator, not separately randomized. Ben Simon’s sleep study connected sleep loss to willingness to help; its donation analysis used a separate aggregate dataset. Crockett 2015i; Strang 2017i; Ben Simon 2022i.

What BERM draws from this

Biological state contributes to social preferences through concrete choices. To reach institutions, BERM composes those choices across people, networks and repeated time steps. The intermediate quantities are participation, effort, trust-bearing actions, sanctioning and withdrawal, each attached to a measured or explicitly modeled outcome.

From individuals to joint action

A biological intervention directed at one interaction partner can change the other partner’s behavior and physiological responses during their interaction.

Joint action needs initiative, a responding partner and temporal overlap. A change in either person alters the pair’s probability of success. Across a population, small changes can accumulate through repeated encounters and thresholds: who meets, who responds, which cooperation succeeds and which relationships continue.

Measured connections

Weisman administered oxytocin to fathers and measured father–infant interaction; changes appeared in infant behavior and physiological responses as well as in fathers. In a separate school-network experiment, Paluck showed that the placement of participating students in the network mattered for changes in community conflict reports. The first study locates an acute interpersonal transition; the second locates propagation through a social network. Weisman 2012i; Paluck 2016i.

What BERM draws from this

A biologically changed action becomes part of another organism’s input. Repeated across a network, this creates changes in the distribution of opportunities and actions. Institutions persist through those actions and their stored consequences; their rules and technologies feed back into later biological and material environments.

Synthetic timing example

Joint action needs two compatible windows

Two fictional people have equally long periods of availability. Shift person B’s window to explore the timing opportunity for a shared task.

Two neutrally drawn people and a worktable for a shared task. Their sex, hormone state and choices are not specified in the picture.
Person A · available5–13
Person A · available. Interval: 5–13.
Person B · available9–17
Person B · available. Interval: 9–17.
Shared time9–13
Shared time: 4 time units. Shared interval: 9–13.
Example shared-task period · relative time

Original timing: 0

Shared time: 4 time units. Shared interval: 9–13.

The overlap is a timing opportunity in this example. It is not a reproduction percentage, a probability of actual action or a prediction of an EMF effect.

  1. Opportunity to encounter

    Both have time together. Goals, willingness and consent are separate conditions.

  2. Measurable event

    Record an initiative, a response and an actual shared task. A time window does not yet tell us what people do.

  3. Outcome to follow

    Follow repetition and the interaction network. One pair does not represent population or institutional change.

What does this example calculate, and what is measured next?

Calculation: max(0, min(end A, end B) − max(start A, start B)). A spans 5–13 and B initially spans 9–17. The control shifts only B; both durations stay at eight. The scale does not represent a particular species’ days or a human circadian rhythm.

Moving from an individual to a pair and a wider group requires records of encounters, choices, repetition and networks. Hormones, motivation and population outcomes are not calculated from this time window.

In BERM’s conditional chain, a timing change could enter through a specified receiver response. This illustration begins with two assumed time windows: the shift is neither derived from a field nor calibrated with biological data.

From individuals to joint action: studies and the BERM interpretation

One state, several connected consequences

BERM derives physiological and behavioral outputs from a shared time-dependent biological state; the field-to-state coupling is the separately specified upstream step of the chain.

Vj=pj(S,L)Bj(S,L)wE,j(S)EjwH,j(S)HjCjV_j=p_j(S,L)B_j(S,L)-w_{E,j}(S)E_j-w_{H,j}(S)H_j-C_jP(a=j)=softmaxj ⁣(β(S)Vj)P(a=j)=\operatorname{softmax}_j\!\left(\beta(S)V_j\right)

This proposed BERM composition separates success probability p, experienced benefit B, effort E, harm H and external cost C. Their weights depend on biological state S; L denotes learning history. Choice probabilities depend on the resulting values V. Shared states constrain several outputs together; the expressions become quantitative only when their variables and coefficients are tied to a particular dataset.

For an intentional reproductive attempt, birth probability composes initiation, conception conditional on the attempt, and live birth conditional on conception. The chain uses conditional probabilities rather than an independence assumption. Total births also include pregnancies that begin without an intentional attempt. Pair distributions and the life-course calendar carry both branches into population outcomes.

Explore the connected explanations

Continue the explanation

From actions to civilization

Follow individual distributions through pairs, networks, populations, institutions and historical feedback.