Introduction

The study of animal behavior is essential for comprehending the intricacies of behavioral dynamics and their underlying cognitive processes. Exploring the neurobiological foundations of animal behavior enables the identification of shared neural mechanisms governing decision-making, learning, memory, and problem-solving throughout the broader spectrum of the animal kingdom. However, investigations of the neurobiology of ecologically valid behaviors can be extremely challenging using traditional approaches. With the rapid advancements in methods for recording and manipulating neural activity from these species, there arises a critical need to modernize our approaches to studying animal behavior to ensure they keep pace with the evolving neural techniques^1-3.

There is growing recognition of the common marmoset’s (Callithrix jacchus) potential as an invaluable animal model in neuroscience research ^4,5 as evidenced by efforts to create marmoset brain databases at multiple biological levels ^6-9. Marmosets provide notable advantages as research models, including their immediate relevance to humans given their genetic relatedness and shared dominant sensory modalities^4,10, and their small size which facilitates naturalistic, freely moving studies of primate social behaviors that can be challenging with larger species like macaques. Further, they offer a unique platform for the study of social behaviors due to their significant parallels with human social structures. Marmosets are particularly prosocial and socially tolerant primates that, like humans, engage in pair bonding and cooperative breeding ^11-14 which has been theorized to have significantly shaped socio-cognitive abilities. Indeed, marmosets consistently show more socio-cognitively advanced behaviors such as social learning, vocal communication, understanding and use of gaze cues, and cooperative problem solving relative to non-cooperatively breeding primates ^{15,16 17-19}. As primates, marmosets also share significant similarities to humans in their neural circuits involved in social cognition ⁴. For example, both humans and marmosets show similar face-responsive brain regions in the temporal lobe ^20,21 and similar brain networks comprising the social brain ^22,23. Marmosets provide a unique opportunity to investigate social behavioral dynamics, however, being a relatively new model in the field of neuroscience, they have yet to benefit from the extensive methodological developments available for other model organisms like rodents. Continued innovation in research methods is essential to fully utilize marmosets as a model system to study complex behaviors and their neural correlates.

Within the realm of animal behavior studies, investigating the dynamics of social interactions and decision-making presents both a challenge and a promising avenue for investigating complex cognitive processes. Advanced social cognition demands constructing and flexibly updating internal models of social agents and computing multiple layers of information across self and others^24,25. In particular, cooperation, a key behavioral strategy crucial to the evolution of advanced social cognition, involves integrating complex information like social relationships and the goals and intentions of oneself and others ^{26-29 30-34}. Given the theorized role of cooperation in the evolution of higher-order cognitive processes involving processing and engaging in social interactions, studying this behavior can have important implications for understanding social dynamics, communication, and cognition in the animal kingdom ^15,35,36.

Traditionally, researchers have studied cooperative behaviors using the cooperative pulling paradigm, a widely employed experimental setup in several animal species that requires animals to collaborate to manipulate a device and retrieve a food reward ³⁷. This paradigm involves two animals working in tandem, each pulling one end of a rope looped through rings attached to a heavy board on the ground. Because the food board is either too heavy for one animal to move alone or rigged so that one animal pulling the rope does not move the board, only coordinated actions can lead to successful food acquisition. This well-established paradigm has greatly contributed to our understanding of cooperative abilities across diverse species, including, but not limited to, chimpanzees, capuchins, hyenas, wolves, dogs, elephants, and rooks ^17,37-43.

While the cooperative pulling paradigm has been invaluable in shedding light on cooperative behaviors across a variety of species, it presents several limitations that hinder its utility for investigating complex behavioral dynamics and preclude studies of underlying neural mechanisms. One notable limitation is the relatively low resolution of behavioral output variables typically measured in the traditional pulling paradigm. Researchers often categorize outcomes in terms of broad categories of successful or unsuccessful cooperation attempts, which may not capture the nuances of behavior with the precision required for advanced analyses. Moreover, manual coding of animal behaviors within the task is constrained to second-by-second measurements and necessitates substantial human labor and expertise.

Additionally, the traditional cooperative pulling paradigm requires frequent experimenter intervention to reset the apparatus’s position and reload it with food rewards between trials. This time-consuming process not only disrupts the natural behaviors of the animals but also limits the number of trials that can be conducted in each session, often allowing for only a meager sample size. For example, from a sample of five experiments employing a traditional cooperative pulling task across a range of species, animals performed, on average, 10.4 trials per session ^17,38-43, which poses a significant challenge for neural investigations. Furthermore, the manipulability of task variables is constrained in this manual setup, hampering researchers’ ability to investigate if and how specific factors influence cooperative behaviors in a controlled manner.

Here, we introduce an innovative method for studying cooperative behaviors in common marmosets (Callithrix jacchus) using an automated apparatus and task. Our Marmoset Apparatus for Automated Pulling (MarmoAAP) for studying cooperative behaviors comprises response levers controlled by a precision servo motor, integrated with a suite of custom-designed components and sensors. Notably, MarmoAAP offers immense versatility, as it can be seamlessly programmed to accommodate a wide spectrum of behavioral tasks. We demonstrate its utility in the investigation of cooperative behaviors, highlighting its capacity to elicit a large number of trials within a single session while producing exceptionally granular behavioral readouts suitable for sophisticated analytical approaches. This not only surmounts the constraints of traditional methodologies but also aligns with the advanced tools now available for scientific research.

Materials & Methods

Apparatus Design & Construction

We developed an apparatus for an automated version of the cooperative pulling paradigm for marmosets (Fig. 1). In this setup, two marmosets are placed in transparent behavior boxes atop the behavioral rig. The marmosets are freely moving in these boxes and have full access to pull levers in front of them. They can reach out and pull the levers at any time. The levers are controlled by an assembly of components that allow us to program rotational force and measure the position and force of the lever at a sub-second level. Additionally, there are five GoPro cameras and two microphones to capture video and audio recordings, respectively.

Figure 1.

The base frame of this apparatus is constructed of modular T-slotted framing and connectors (Fig. 1A, C). The main structure of the base is a table measuring 18” h x 24” w x 18” l. The table consists of four legs supporting two sets of horizontal rectangular framing. The rectangular frames have T-slotted rails running from front to back, and the lever assembly is attached to these rails. T-slotted framing was also used to provide arms extension to hold the GoPro cameras in the appropriate position (Fig. 1A, C).

The core of the apparatus is the assembly that controls the marmosets’ pulling levers (Fig. 1B). This assembly is constructed from the materials listed in Table 1. The movement of each pull lever is controlled by a servo motor that is programmed via microcontroller development boards (Teensy). With custom code (Arduino), we can exert rotational force on the levers via motor control. This enables us to change the force with which marmosets must pull the levers. It also allows us to reset the levers to the starting positions after the marmosets have pulled the levers. The levers are also connected to two sensors, a strain gauge and a potentiometer. The strain gauge converts the force exerted onto the lever into an electrical signal. The potentiometer measures the position of the lever in a rotary motion and converts it into an electrical signal. These signals can be transmitted to a computer via the Teensy board and used in the task code to evaluate the marmosets’ lever-pulling actions and contingently trigger reward delivery from the syringe pumps (New Era / DUAL-NE-1000X). A successful lever pull is determined by the lever position passing a specified positional threshold as determined by the potentiometer reading. For the Mutual Cooperation condition, a pair of lever pulls is considered successful when the second lever pull has passed the positional threshold within 1 second of the partner’s lever having passed the positional threshold.

Table 1.

The lever-motor assembly also consists of structural components that hold each component in the appropriate position. The servo motor is attached to the base frame with a custom-designed mounting plate. A custom-designed clamp sits around the shaft of the motor and serves to yoke the strain gauge and pull lever to the movement of the motor shaft. The top side of the strain gauge connects to the top side of the clamp, and the lever is then connected to the opposite end of the strain gauge. This enables lever force reading by the strain gauge each time the lever is pulled. The bottom side of this clamp is attached to a counterweight (Fig. 1B). Positioned directly opposite to the motor shaft is the potentiometer (Fig. 1B). The potentiometer is yoked to the motor shaft such that when the lever moves, and therefore the motor shaft rotates, the potentiometer shaft also rotates. This ensures that the potentiometer shaft movement and therefore the potentiometer readings correspond to lever movement. To achieve this, we use a 3D-printed potentiometer-motor adapter. One side of this adapter fits onto the motor shaft and the other side fits onto the potentiometer shaft. Both shafts are held securely in place with a set screw.

Finally, the body of the potentiometer must be held in a stable position so that it does not also move when the potentiometer shaft rotates. To achieve this, we designed a potentiometer mounting plate. This plate has two holes such that crossbars can be attached to connect this potentiometer mounting plate to the motor mounting plate. Additionally, it has a hole that the potentiometer shaft is passed through, and a smaller hole that the tab on the potentiometer body can be placed in. This tab holds the potentiometer in a fixed position to prevent the potentiometer body from rotating when the potentiometer shaft rotates.

Animals

We trained a total of 7 adult common marmosets (Callithrix jacchus) (3 males, 4 females; 6.0 ± 1.7 years, mean ± s.d.) to perform the MarmoAAP lever-pulling tasks. All marmosets were either pair- or group-housed and lived in the same colony room with a 12-hour light-dark cycle. All pairs tested together were familiar cage-mates. Before testing sessions, water access was temporarily removed, and the AM feed was withheld for 1-3 hours. Water and food were given upon return to the home cage after testing at which point animals had unrestricted access to both. All procedures were approved by the Yale Institutional Animal Care and Use Committee and complied with the National Institutes of Health Guide for the Care and Use of Laboratory Animals.

Behavioral Training

Marmosets were first trained to voluntarily enter a transport box. At this stage, they were also trained to target and touch the metal rod used for the apparatus’ lever from their home cage in exchange for a marshmallow or mealworm reward. Once marmosets were comfortable entering the transport box, they were habituated to transportation to the testing room and sitting inside the transport box in the room. During training, marmosets were always transported and habituated in cage-mate pairs. Once comfortable in the testing room, marmosets were habituated to the transparent behavior boxes (Fig. 1A) and trained to pull the levers (Fig. 1A) on the apparatus in exchange for a liquid reward (marshmallow fluff diluted with water; 6 g marshmallow fluff per 20 ml water).

Next, marmosets were trained to perform the Self-Reward task. For this task, marmoset pairs were placed in the transparent behavior boxes side-by-side, and each was free to pull their lever at any time in exchange for 0.1 ml of liquid reward. The pull-reward contingency was fully independent across the two marmosets. A monitor in front of them depicted a white square cue for this task (Fig. 1C). Once they reliably performed the Self-Reward task, we began training them to perform the Mutual Cooperation task. For this task, we introduced a contingency requiring that they pull their levers within a certain time window of one another to receive mutual liquid rewards. A yellow circle cue was depicted on the monitor in front of them for this task. Training advanced through incremental decreases in the cooperative time window including 3 seconds, 2 seconds, then 1.5 seconds, and finally 1 second. A pair of lever pulls in this condition was deemed successful cooperation if the levers were both pulled past their position thresholds within the cooperative time window. After the follower pulled their lever on a successful pull, a tone was played immediately and 0.2 ml of liquid reward was delivered to both animals 1 second later.

Head Chamber Implantation & Craniotomy

One animal received a head chamber implant and craniotomy. After the head chamber was surgically implanted, the animal was allowed to recover for 2 weeks. After the recovery, a second procedure was performed to create a craniotomy and mount a screw microdrive (‘nanodrive’; Cambridge Neurotechnologies Inc.) holding a 64-channel linear array electrode (NeuroNexus) onto the skull of the marmoset. Craniotomy placement was guided by CT scans and stereotaxic coordinates. The electrode’s electronic interface board was then connected to the White Matter eCube headstage chips (White Matter LLC) which were secured in the marmoset’s head chamber. The implanted electrode was then lowered into the desired cortical site.

Neural Recordings

Recordings were logged using White Matter’s eCube headstage system. At the beginning of each recording session, the marmoset was restrained, but not head-fixed, in a chair, and the White Matter’s data logger was connected to the headstage chips in the head chamber. The logger was secured in place with a cap. The marmoset was previously habituated to this restraint process, and the process typically lasted approximately 5 minutes. The marmoset was then placed in the transparent behavior box and allowed to engage in the behavioral task with his partner. On neural recording days, behavioral sessions consisted of one block of the Mutual Cooperation task and one block of the Self-Reward task, each lasting approximately 10 minutes. After the behavioral testing, the marmoset was again placed in the chair for removal of the data logger. Electrical signals were collected at 20kHz from the probe. Action potential waveforms were extracted using Kilosort2 ⁴⁴ and manually sorted into single-units and multi-units using phy.

Results

Marmosets perform high number of trials on automated lever-pulling tasks

The implementation of MarmoAAP yielded significant advancements in the ability to study complex behaviors in marmoset monkeys. In the initial phase of our study, we successfully trained a cohort of 7 marmosets to perform the Self-Reward condition in which they could pull their lever at any time to earn a 0.1 ml juice reward for themselves. On average, marmosets pulled 163 ± 56 (mean ± s.e.m.) times per 20-minute behavioral session demonstrating high levels of motivated behavior (Fig. 2A). This training phase thus demonstrated the marmosets’ capacity to acquire and consistently execute lever-pulling behavior, providing a dependable means to elicit a high number of motivated and appetitive behaviors.

Figure 2.

Building upon this foundation, we extended our investigations to more complex tasks requiring cooperative pulling behaviors. We trained three unique dyads of familiar marmosets to perform cooperative pulling. For the Mutual Cooperation condition, we introduced a contingency that requires both marmosets to pull their levers within a specified time window of one another to both earn juice rewards. This task is completely unconstrained such that marmosets were free to pull their levers at any time. If the marmosets pulled their levers within the one-second cooperative time window, a tone was played, and 0.2 ml of juice reward was delivered to both marmosets. However, if they pulled their lever and their partner did not pull within the cooperative time window, they were not rewarded.

We observed that all three dyads achieved proficiency (50% success rate; defined as the number of pulls resulting in successful cooperation out of all pulls by both animals) in this cooperative task within a two-month period. The average number of training days to reach Mutual Cooperation proficiency was 33.7 ± 11.9 days. This learning progression was further characterized by quantifiable metrics reflecting their progression in learning the cooperative contingency. Using the precise time stamps of the behavioral events (Fig. 2B), we calculated three metrics across six example sessions (3 Self-Reward sessions, 3 Mutual Cooperation sessions) that differentiated marmosets’ performance on the Self-Reward and Mutual Cooperation tasks (Fig. 2C). Notably, the utilization of the automated behavioral paradigm enabled marmosets to perform an average of 146 trials per 20 minute behavioral session (successful cooperation = 47.9 ± 3.3 trials [mean ± s.e.m.]; unsuccessful cooperation = 98.9 ± 6.6 trials) (Fig. 2A), a substantial improvement compared to the average of 10.4 trials per session observed in studies employing more manual cooperation paradigms. This heightened throughput, coupled with high repeatability, emerges as a critical asset for dissecting the intricacies of behavioral dynamics and the neural computations underlying complex behaviors.

Customizable task parameters allow for adaptation to marmosets’ abilities

Our behavior training also underscored the importance of task parameter adjustability in optimizing marmosets’ performance. We tailored MarmoAAP to individual marmosets by fine-tuning parameters such as the distance required for a lever pull to register as a full pull and the force needed to initiate the lever-pulling action. By initially reducing the force required to pull the lever to 50 g, marmosets were able to smoothly transition into learning the task. Once they became habituated to the lever-pulling paradigm, we increased the lever-pulling force to 100 g and maintained this force level for Self-Reward and Mutual Cooperation tasks.

Additionally, we customized the reward magnitude offered for task completion to suit the specific requirements of the cooperative pulling task. For example, while marmosets exhibited motivation to work for a 0.1 ml juice reward in the individual pulling task, this was often not sufficient to elicit consistent pulling behaviors from dyads in the more difficult cooperative task. However, increasing the reward amount to 0.2 ml elicited enhanced motivation and more consistent cooperative behaviors from all three dyads. This adaptive parameter manipulation contributed significantly to the success of our marmoset dyads in mastering the cooperative pulling task, highlighting the importance of tailoring task parameters to individual and task-specific requirements.

Furthermore, MarmoAAP can easily be adapted to a wide variety of behavioral paradigms both in terms of the hardware configuration and parameters set by the task code. Given the modular nature of the apparatus design, the assembly can easily be adjusted to increase or decrease the number of pull levers as well as to change their configuration relative to one another. The task requirements imposed on the animals can also be easily adjusted by changing the task code. For example, the cooperative pull timing contingency, the force required to pull the lever, lever pull distance, and reward timing are just a few examples of task parameters that can be adjusted through the task code. One can imagine a wide variety of experiments that could be achieved with this apparatus to test cognitive processes such as but not limited to observational learning, memory, competition, altruism, executive function, and a host of other motivated behaviors.

High-resolution behavioral data allows for advanced analyses

MarmoAAP facilitates comprehensive collection of detailed behavioral data across a variety of modalities. Its design allows for the capture of sub-second level outputs detailing lever positioning (Fig. 2B) and the force applied to the lever. Additionally, it can be built to support cameras to record multiple angles for video data collection and incorporate microphones to record audio. Leveraging this video data, we used automated behavioral marking tools like DeepLabCut2 (DLC2) ^45,46 to obtain frame-by-frame annotations of the marmosets’ head frames (Fig. 2D). This rich dataset serves as a foundation for subsequent analyses, including the exploration of inferred gaze direction, spatial location within the enclosure, and overall movement trajectories.

In particular, we would like to highlight our ability to analyze gaze dynamics in this platform. Gaze behaviors are fundamental to social behaviors of primates which are highly visual animals. We were able to analyze complex behavioral dynamics by employing DLC2 to track the head frames of each freely moving marmoset as they engaged in the pulling task. We then used Anipose to create a 3D reconstruction of the marmosets’ head frames based on videos from 3 cameras⁴⁷. Based upon the constructed head frames, we estimated the marmosets’ gaze direction by creating a virtual cone with an axis perpendicular to the plane defined by markers for the marmosets’ eyes and forehead and a solid angle of 15 degrees. Using this approach, we were able to quantify the number of gazes towards various targets during the sessions. Using data from three example sessions, we can quantify bouts of gazes at targets of interest including their partner (social gaze), lever, and juice tube (Fig. 2E). Such additional information that can be obtained within the automatic pulling paradigm can be used to better understand complex social interactions in marmoset pairs or groups.

Recognizing the highly vocal nature of marmosets and their extensive repertoire of vocalizations, each with distinct functions, we also collected audio recordings of every behavioral session. We were able to capture a wide variety of marmoset vocalizations during this task. Here, we specifically focused on chirp, trill, and phee calls (Fig. 2F). Using the timestamps from the lever pulls and reward delivery, we further analyzed vocalizations relative to task events. As an example, we examined vocalizations relative to successful and unsuccessful lever pulls from one marmoset across 19 sessions (6 Self-Reward sessions, 13 Mutual Cooperation sessions) (Fig. 2G). This marmoset showed an increase in chirp calls, known to serve as food calls^48,49, after lever pulls in Mutual Cooperation sessions compared to Self-Reward sessions.

By incorporating these behavioral metrics from video and audio recordings with the timing of marmosets’ pulling behaviors and reward delivery, one can gain a more comprehensive understanding of the intricate interplay between behavior, vocal communication, and cooperative interactions in this species using an automated pulling task.

Precise synchronization with reproducible behavior allows behavior-locked neural data analyses

In addition to providing rich behavioral data and offering flexibility for various tasks, MarmoAAP and associated behavioral paradigms create an avenue for simultaneous neural recordings while freely moving marmosets are engaged in tasks implemented by MarmoAAP. MarmoAAP significantly increases the number of trials available for analysis and thus ensures ample statistical power when investigating the relationship between neural activity and behaviors. The highly reproducible lever-pulling behavior in marmosets within a naturalistic context strikes a crucial balance between conventional laboratory tests, where monkeys are immobilized and tasks lack natural movement but are tightly controlled, and more naturalistic animal behavior studies, where animals exhibit unrestrained behavior but lack regular behavioral benchmarks for studying the underlying neural dynamics ^50,51.

To validate this application of MarmoAAP, we conducted wireless neural recordings using a silicon-based linear array probe while a marmoset engaged in the cooperative pulling task with its partner (Fig. 3A) and were able to isolate single unit activity from the prefrontal cortex (Fig. 3B). On each day, marmosets performed a 10-min session of the Mutual Cooperation task and a 10-min session of the Self Reward task. By synchronizing the behavioral and neural activity timestamps, we were able to investigate spiking activity relative to various behavior events. Here, we present an example single unit recorded from the orbitofrontal cortex (OFC) and an example multi-unit from the dorsolateral prefrontal cortex (dlPFC) that showed increased firing rates around lever pulls in a Mutual Cooperation session (Fig. 3C-D). Investigating neural activity with specific yet naturalistic behavioral events provides a valuable dataset for investigating the neural dynamics associated with cooperative interactions. By using wireless electrophysiology recording techniques in conjunction with this cooperative behavior paradigm with markerless behavioral tracking, one can obtain a more comprehensive understanding of the neural underpinnings of complex social behaviors, such as cooperation.

Figure 3.

Discussion

The Marmoset Automated Apparatus for Pulling (MarmoAAP) bridges the gap between traditional animal behavior methodologies and the demand for increased precision and adaptability in behavioral research. To advance our understanding of the complex behavioral and neural dynamics underlying cooperative behaviors, it is imperative that we transition toward a modernized approach to examining animal behaviors. In our current work, we introduced a novel automated cooperative pulling apparatus designed to address these limitations and advance the study of cooperative behaviors by providing a more refined and manipulable platform for experimentation. MarmoAAP offers the ability to enhance behavioral resolution in data collection, increase data output, streamline experimental procedures, and provide the flexibility to systematically manipulate task variables. With this scalable tool, researchers can gain insights into the behavioral dynamics governing cooperative behaviors and the neural mechanisms that underlie these complex social interactions. This methodology not only holds exceptional promise for enriching our understanding of primate behavior but also provides a unique opportunity to explore the intricate connections between neural processes and actions in a manner that bridges controlled and naturalistic experimental conditions.

The development of MarmoAAP arrives at a critical time, coinciding with burgeoning efforts to engineer genetically modified marmosets^52-55. As such models progress, it is essential to have robust methodologies that can accurately measure the features of marmoset social interactions. Precise behavioral assays are indispensable for future investigations aiming to elucidate the effects of genetic modifications on social behavior and test potential therapeutic approaches. Just as neurological abilities such as locomotion can be quantitatively assessed⁵⁶, it is critical to establish equivalent metrics for evaluating complex behavioral patterns in marmosets.

Automated Task Paradigm for Naturalistic Social Exploration

Using MarmoAAP, we were able to elicit consistent and highly repeatable motivated behaviors in freely moving marmoset monkeys. This task design strikes a pivotal balance between traditional naturalistic animal behavior studies, which benefit from a high degree of naturalism but often suffer from low behavioral resolution and limited trial counts, and conventional lab studies, which are highly controlled but lack natural ethological relevance ⁵⁰. Previous research has underscored the substantial impact of behavioral context, specifically the distinction between constrained and freely moving conditions, on prefrontal cortical representations of social information ⁵⁷. Our shift towards a paradigm that integrates naturalistic, yet highly repeatable, decisions and actions is imperative for the comprehensive exploration of natural social behaviors and the elucidation of their underlying neural mechanisms. This approach addresses the limitations of paradigms that fall short of faithfully capturing the intricacies of social interactions, emphasizing the importance of a more ecologically valid framework for advancing our understanding of the neural dynamics that underpin fundamental aspects of primate social brain functions.

Quantification of High Throughput Cooperative Behaviors

We show that marmosets exhibit a rapid acquisition of proficiency in the lever-pulling action and demonstrate their capacity to grasp more complex task contingencies, such as the cooperative pulling task highlighted in this study. Our findings also showcase that the detailed behavioral data outputs from the apparatus, including sub-second timestamps for lever pulls and reward deliveries, enable us to quantitatively assess marmosets’ learning and performance on this task. Significantly, our study demonstrates that the automated apparatus facilitates a substantial 15-fold increase in the number of trials conducted per session compared to conventional pulling paradigms. This increased trial throughput is of critical importance for investigations of the neural mechanisms underlying these social behaviors, ensuring the acquisition of a robust dataset for comprehensive analyses of neural activity during naturalistic behavioral settings. Moreover, the ability to examine complex social interactions with high throughput data might be particularly important for characterizing transgenic marmoset models.

Manipulability and Adaptability of Task Parameters

Importantly, the configuration of MarmoAAP allows for precise adjustment of task parameters, a key feature for optimizing marmoset performance and facilitating investigations into a diverse array of complex behaviors. Experimenters can easily fine-tune parameters in the task code to customize apparatus functionality for various behavioral tasks or to accommodate the specific needs and capabilities of individual animals. This adaptability not only expedites the animal training process but also allows for a nuanced exploration of the intricate dimensions of cooperative behaviors, ensuring that experimental conditions closely align with research objectives. Such flexibility is indispensable not only for cooperative tasks but also positions our paradigm as a versatile tool for delving into cognitive processes beyond cooperation.

High-Resolution Behavioral Data and Multimodal Analyses

In tandem with the intricate behavioral outputs derived from the apparatus, MarmoAAP incorporates the integration of information from many sources and modalities. Utilizing video recordings obtained during the task, we showcased the application of automated behavioral marking tools, such as DLC2 ^45,46, to probe the interplay between behavioral dynamics—particularly gaze behaviors—and performance on the cooperative task. Complementarily, the inclusion of audio recordings enriches this dataset, allowing for a comprehensive examination of marmosets’ vocal communication patterns and their correlation with task events. This multimodal approach establishes a robust foundation for nuanced investigations into the cognitive processes and social dynamics of marmosets, aligning with a goal toward a comprehensive understanding of primate social behaviors.

Integration with Neural Recordings

A key attribute of the MarmoAAP design is its capacity to seamlessly integrate with wireless electrophysiology recordings, providing an avenue to explore the neural underpinnings of behavioral processes. The apparatus allows for precise time-locking of task and behavioral events with neural activity as demonstrated in the dlPFC and the OFC. With a substantially increased number of trials amassed through MarmoAAP, this demonstration supports the possibility of examining the neural dynamics underlying cooperative behaviors in marmosets. Our apparatus and paradigm represent a noteworthy advancement, bridging the gap between traditional animal behavior studies that address ethologically relevant behaviors of animals and precise, highly controlled investigations of neural activity.

Conclusion and Future Directions

In conclusion, we hope that MarmoAAP and the associated automated cooperative pulling paradigm will make a significant contribution to the study of marmoset social behaviors in the field. The combination of a highly modular and adaptable design, high-resolution behavioral data, and integration with neural recordings positions our paradigm as a robust and versatile tool for unraveling the complexities of primate behavior. As we move forward, this paradigm not only serves as a platform for in-depth investigations into marmoset social dynamics but also holds the promise of extending our understanding of cognitive processes and neural mechanisms across a variety of complex behaviors. The scientific community can leverage this paradigm to explore a myriad of cognitive processes, from observational learning to executive function, laying the groundwork for comprehensive insights into the neural mechanisms of complex behaviors in nonhuman primates.

Acknowledgements

This work was supported by the National Science Foundation Graduate Research Fellowship (DGE2139841, O.C.M.), the National Institute of Mental Health (R21 MH126072, S.W.C.C., A.S.N., M.P.J.), and the Simons Foundation Autism Research Initiative (SFARI 875855, S.W.C.C., A.S.N., M.P.J.). We thank Paul Shamble and the Neurotechnology Core of the Kavli Institute for Neuroscience at Yale University for providing technical support. We also like to thank Feng Xing and Amrita Nair for their support in this research project.

Author Contributions

O.C.M., A.S.N., S.W.C.C. conceptualized the paradigm, N.A.F. wrote the apparatus control and task code, and O.C.M., W.S., M.P.J., A.S.N., S.W.C.C. analyzed and wrote the manuscript.

Competing Financial Interests

The authors declare no competing financial interests.

Data Availability

Code for the automated pulling tasks can be found at https://github.com/changlabneuro/cooperative-pulling-task/. CAD files for apparatus parts can be made available upon request.

Note

This reviewed preprint has been updated to add a co-corresponding author and update the text in the Author Contributions.