Bipedal trackways discovered in 1978 at Laetoli site G, Tanzania and dated to 3.66 million years ago are widely accepted as the oldest unequivocal evidence of obligate bipedalism in the human lineage1,2,3. Another trackway discovered two years earlier at nearby site A was partially excavated and attributed to a hominin, but curious affinities with bears (ursids) marginalized its importance to the paleoanthropological community, and the location of these footprints fell into obscurity3,4,5. In 2019, we located, excavated and cleaned the site A trackway, producing a digital archive using 3D photogrammetry and laser scanning. Here we compare the footprints at this site with those of American black bears, chimpanzees and humans, and we show that they resemble those of hominins more than ursids. In fact, the narrow step width corroborates the original interpretation of a small, cross-stepping bipedal hominin. However, the inferred foot proportions, gait parameters and 3D morphologies of footprints at site A are readily distinguished from those at site G, indicating that a minimum of two hominin taxa with different feet and gaits coexisted at Laetoli.
In 1976, Peter Jones and Philip Leakey discovered five consecutive bipedal footprints at Laetoli site A within locality 7, a 490 m2 area dated to 3.66 million years ago (Ma) and featuring 18,400 animal tracks1,2,3 (Fig. 1). Mary Leakey tentatively suggested that the trackway was made by a hominin1. “The footprints,” she wrote, “indicate a rolling and probably slow-moving gait, with the hips swivelling at each step, as opposed to the free-striding gait of modern man [humans].” Leakey and Hay2 classified the footprints as Hominidae, but with a caveat that “the gait was somewhat shambling, with one foot crossing in front of the other.”
Unequivocal hominin footprints were discovered at site G two years later, casting doubt on the hominin status of those at site A3,4,5. Researchers described the footprints at site A as “most unusual,”6 “curiously shaped,”7 and “enigmatic,”8 and yet consensus was uniform: they were produced by a plantigrade mammal moving bipedally.
Tuttle4 advanced three hypotheses to account for the morphology of the footprints and cross-stepping gait (that is, when a foot from each side crosses the midline before touchdown): (1) substrate distortion; (2) they were left by a juvenile bear (ursid); or (3) they are evidence of another hominin species. To test the second possibility, Tuttle4,9,10,11,12 collected data from circus bears trained to walk bipedally and found that their short steps and relatively wide feet were a close match to the site A footprints, although bipedal bears take wider steps. Furthermore, the fifth digit is typically the largest in ursids, solving the ‘cross-stepping problem’, although Tuttle4,12 noted that humans do occasionally cross-step. He concluded that “until detailed, naturalistic biometric and kinesiological studies are performed on bipedal bears and barefoot humans, we will have to defer choosing among the hominid and ursid hypotheses on Laetoli individual A”4.
Complicating matters further, the internal morphology of the site A footprints was never fully cleaned of matrix infill1,2,4,5,12. White and Suwa8 argued that “reliable identification of these enigmatic prints at Laetoli site A will be impossible until they are more fully cleaned and followed laterally”. Accordingly, we were motivated to relocate and re-excavate site A and conduct a detailed comparative analysis of the prints as well as the locomotion of bears (Ursus americanus), chimpanzees (Pan troglodytes) and humans to test whether the footprints at site A were left by a hominin or an ursid.
Rediscovery of site A
Using detailed maps from Leakey and Harris3, we identified the proboscidean trail adjacent to the bipedal footprints. We cleared the surrounding overburden until one of us (K.F.) found the A3 footprint. The area was then brushed clean to expose A1–A5, which have experienced no discernible erosion since their initial discovery (Fig. 1, Extended Data Fig. 1). Because the footprint tuff is eroded to the north, we excavated south (87 cm) and east (54 cm) from the heel of A1, but no additional footprints were found (Supplementary Information).
After brushing sediment from A3, we used a wooden tongue depressor to remove tuff infill left intact during the 1976–1978 field seasons. The hallucial impression is clearly defined and is about 30 mm wide. Crucially, we exposed the impression of the second digit (Extended Data Fig. 2). We removed infill from A2 but could not do so completely without risking damage. Nevertheless, the heel and hallucial impression are clear. Detailed information from the other footprints (A1, A4 and A5) is limited to estimates of length, width and step length.
Although preservation quality varies within and between A1–A5, there is no evidence that biologically informative metrics were affected by substrate distortion. Adjacent and comingled tracks of other animals (ranging in size from guinea fowl to elephants) show no evidence of distortion to their perimeters or internal morphologies. Given that track surfaces are likely to represent time scales of hours to days13,14,15, it is parsimonious to infer similar substrate conditions and taphonomic processes during print formation and subsequent epochs.
Evaluating ursid and hominin hypotheses
We recorded 50.9 h of video of wild American black bear behaviour. Unsupported bipedal posture and locomotion occurred only 0.09% of the total observation time, of which 59% was postural and 41% was locomotor (Extended Data Fig. 3). In only one instance did a bear take four unassisted bipedal steps. Thus, assuming that our findings are generalizable to other ursids, the probability of observing four consecutive bipedal steps is 0.003%. The low frequency of this behaviour, and the absence of quadrupedal–bipedal transitional footsteps, makes it unlikely, but not impossible, that ursid bipedalism was preserved at site A. Further, Laetoli is devoid of ursid fossils despite the recovery of more than 25,000 fossils attributed to 85 mammalian species16,17. If present at all, ursids were rare on the landscape. Although footprint assemblages can include a surprising number of tracks from taxa whose skeletal fossils are rare (for example, relatively high frequencies of bird tracks at Laetoli3 and at 1.5-Ma sites near Ileret, Kenya14,18), there is no clear taphonomic explanation for why ursid tracks would be present but their fossils absent.
In addition, we measured 46 footprints from four bipedally walking wild juvenile black bears specifically chosen because their foot lengths (mean = 145.7 mm) were within 10% of the length of the site A footprints (mean = 161.7 mm). Additionally, we measured the footprints of chimpanzees produced during quadrupedalism (n = 54 from 46 adults; Ngamba Island Chimpanzee Sanctuary, Uganda) and during bipedalism (n = 44 from two subadults; Stony Brook University, USA). We compared these data with human barefoot footprints produced under three conditions: (1) habitually shod (n = 654) walking on a plantar pressure mat19; (2) habitually unshod or minimally shod (n = 41) walking in deformable mud20,21; and (3) Late Pleistocene tracks (n = 113) from Engare Sero, Tanzania, formed in reworked volcanic ash22,23 (summary in Extended Data Table 1).
We concur with others4,12 that the ratios of footprint dimensions (for example, heel and forefoot width) to step length observed at site A fall within the ursid range (Extended Data Fig. 4a, b). Yet, for these same measures, site A is also chimpanzee-like and moderately similar to definitive hominin footprints from sites G and S. It follows that the site A individual was taking short steps—as occurs when humans walk slowly or over a slippery substrate24—not that the gait was ursid-like.
With additional infill removed from A2 and A3, the perimeter dimensions are decidedly hominin-like with wide heel impressions relative to forefoot width (Extended Data Fig. 4c). By contrast, chimpanzees and bears have relatively narrow heels. Furthermore, with the tracks fully excavated and cleaned, we found no evidence for claw impressions, although they are sometimes absent from ursid footprints12. Here, impressions were absent from 31% of ursid footprints. To test whether A3 was produced by a hominin left foot or an ursid right foot, we compared the width of the hallux to the second digit in human (n = 30) and chimpanzee (n = 50) footprints, and the fifth digit to the fourth in bear (n = 5) tracks. The A3 toe impressions match the distinctive proportions of humans and chimpanzees rather than those of bears (Extended Data Fig. 5).
By establishing that A3 is a left hominin foot, we can now confirm that cross-stepping occurred. Cross-stepping was never observed in our comparative sample, but humans do it occasionally25,26 as a compensatory strategy for re-establishing balance after a perturbation27. In fact, we suggest that cross-stepping supports the hypothesis that the site A footprints were left by a hominin. Cross-stepping is improbable, and perhaps impossible, when bears or chimpanzees walk bipedally. They produce large mediolateral excursions of their centre of mass28 and walk with highly abducted hips29, resulting in a high ratio between stride width and step length. Conversely, human cross-stepping is enabled by their reduced mediolateral centre of mass and body motions, adducted hips and bicondylar angle (that is, valgus knees), resulting in a low corresponding ratio, as expressed in every trackway at Laetoli.
The relative step widths of footprints from sites G and S fall squarely within the modern human distribution (Extended Data Figs. 4d, 5). The site A footprints lie outside the distributions of humans, chimpanzees and bears but are most like humans. This result indicates that the maker of the site A footprints had either valgus knees or adducted hips, or both. The presence of either bipedal trait argues for a hominin maker of the site A footprints.
It is generally accepted that Australopithecus afarensis produced the footprints at sites G and S8 (but see refs. 12,30,31,32). It is thus tempting to assign the site A tracks to A. afarensis; however, this premise requires an examination of foot ontogeny and intraspecific morphological variation that takes into account the mounting fossil evidence of locomotor (and presumably taxonomic) diversity among Pliocene hominins (for example, in ref. 33).
Standing between 101 and 104 cm tall (from equations in Dingwall et al.34), the maker of the site A footprints was smaller in height than other Laetoli trackmakers, which ranged from 111–116 cm (site G1) to 161–168 cm (site S1)35. It is plausible that the site A tracks were made by a juvenile A. afarensis, but this hypothesis is undermined by a distinct footprint morphology from those at sites G or S.
The ratio of foot width and length follows a different ontogenetic trajectory in humans and chimpanzees; human feet are consistently narrower than chimpanzee feet (Fig. 2). Footprints made by unshod humans from both modern times and the Pleistocene are slightly wider than those made by shod humans in industrialized populations. The undistorted footprints from sites G and S fall within the human distribution. A3 is more chimpanzee-like in being wide compared with its length (Fig. 2a, Extended Data Fig. 2). In chimpanzees, this wider footprint shape is, in part, driven by the greater divergence of the hallux. We thus measured hallucial divergence as a ratio of the distance between the centre of the impression made by the first and second digits and the length of the footprint. For this metric, humans and chimpanzees are clearly distinct. The best-defined site G footprints overlap the human distribution, whereas the A3 footprint does not—it possesses a slightly more divergent hallux than humans and site G, although not nearly as divergent as those of chimpanzees (Extended Data Fig. 6). This finding alone does not rule out a juvenile A. afarensis, given the foot from Dikika (Afar, Ethiopia) has a slightly more divergent and mobile hallux than its adult counterparts36.
To explore other instructive traits, we compared proportional toe depth ratios as described by Raichlen and Gordon37 (Supplementary Methods). The mean value for site A (−0.191) is distinct from Laetoli G1 and humans using a bent-hip bent-knee gait but overlaps the low end of variation in Laetoli S. Additionally, tracks A1–A3 evince a raised ridge of hardened ash between the heel and lateral forefoot. It is unclear whether this ridge is evidence of substrate shearing38 or midfoot mobility—a characteristic absent from the Laetoli G and S footprints39 (but see ref. 40) and inconsistent with A. afarensis pedal remains41.
Finally, we tested whether we could randomly sample footprints with internal topography similar to the various Laetoli footprints from those of humans or chimpanzees (following Hatala et al.42). Fig. 2 illustrates how the tracks from sites G and S can be encompassed in the range of resampled unshod human footprint variation, whereas the average morphology of the A2 and A3 tracks is distinct from the footprints of habitually unshod humans and those at sites G and S. In fact, they fit comfortably within the resampled chimpanzee distribution, being as distinct as chimpanzee tracks are from the morphologies of barefoot human tracks. One possible explanation for such different footprint morphology is that the site A footprints were made by a cross-stepping A. afarensis. We tested this hypothesis by comparing the footprints of humans (n = 10) walking with their preferred gait and then cross-stepping. We found that normal and cross-stepping human footprints differ minimally and do not match in magnitude or direction the differences between the site G and S prints and the site A prints (Extended Data Fig. 7, Supplementary Information).
We therefore conclude that the site A footprints were made by a bipedal hominin with a distinct and presumably more primitive foot than A. afarensis. The gross shape of the foot is chimpanzee-like, with slight hallucial divergence and perhaps some midfoot mobility. However, the site A individual was walking bipedally with a narrow step width indicative of either a valgus knee, adducted hips, or both. This combination of foot morphology and gait kinematics inferred from the preserved footprints precludes them from having been made by A. afarensis.
Evidence is building for taxonomic diversity in hominins during the Pliocene43,44, including at Laetoli45,46,47, but these hominins did not walk with morphologically identical feet48. For example, the BRT-VP-2/73 foot from the 3.4 Ma site of Woranso-Mille, Ethiopia demonstrates that at least two different foot morphs co-existed in the Afar Depression during the Pliocene33. We suggest that footprint evidence for hominin locomotor diversity is similarly present at Laetoli, Tanzania—and has been since the discovery of the site A trackway in the 1970s.
Wild bear behavioural data
Wild black bear behaviour was quantified using video data recorded by B.K. over the course of several years at his ongoing field site in Lyme, New Hampshire, USA. Video data captured bears of different ages (cubs, adolescents and adults). Bears were present on screen for a total of 50 h 55 min 18 s. For each terrestrial bipedal incident, the length of the event, the approximate age of the bear and the number of steps were recorded. Additionally, steps were evaluated on whether they were completed independently, or the individuals used other environmental objects for balance.
Comparative kinematic data
Comparative kinematic data were collected on three species: U. americanus, P. troglodytes, and Homo sapiens. For bears and chimpanzees, the sample size included all available individuals housed at each location. For the human sample size information see below. Randomization was not relevant to our study as we were interested in measuring footprint characteristics from whole sample populations, as opposed to comparisons within those populations. Blinding was not relevant to the data collected on the non-human comparative species (for example, bears and chimpanzees) nor to the data collection on fossilized footprints. The human participants were unaware of the site A tracks at Laetoli and therefore had no knowledge of how the data obtained from their footprints would be used in this study.
Data were collected on four juvenile semi-wild U. americanus (n = 3 male, 1 female), whose feet were within 10% of the length (average foot length = 145.7 mm) of the recorded footprints of Laetoli site A (average foot length = 161.7 mm). These orphaned, approximately 20-kg bears were located at the Kilham Bear Center (Lyme, NH), awaiting reintroduction to the wild. This study examined the bears between the ages of 5–8 months old. Our protocol was reviewed and approved by the Institutional Animal Care and Use Committee (IACUC) of Dartmouth College. The bears were enticed to independently walk bipedally through a constructed mud trackway for either an applesauce or maple syrup reward (Extended Data Fig. 3). Measurements were collected on the footprints, including foot length, heel width, forefoot width, step length and stride width using the definitions from Tuttle4. For a subset of footprints (n = 5), the width of the impression for the 1st, 2nd, 4th and 5th digits were measured. The presence or absence of claw impressions was also documented.
Data for extant chimpanzees were extracted from three sources to collect all the relevant gait metrics. Two published datasets examined the same two subadult individuals housed at Stony Brook University. The third set were recorded on semi-wild individuals (n = 46), using a plantar pressure mat at the Ngamba Island Chimpanzee Sanctuary (Entebbe, Uganda). While this third data set increases sample size and captures intraspecific variation, we recognize that plantar pressure data do not always align perfectly with footprints made in a deformable substrate20.
Stride width data and step length comparisons
Chimpanzee stride width data were taken from Thompson et al.28 on two subadult male chimpanzees (7.0 ± 0.1 years of age; 34.8 ± 1.2 kg) and were supplemented with step length data for the same steps. Three-dimensional kinematic methods and step width calculation have been described previously28. Step length was calculated as the distance between left and right calcaneus markers in the sagittal plane during consecutive hind limb midstance periods. Chimpanzee step lengths are typically asymmetric, so step length was averaged over the two consecutive steps which defined the stride.
Forefoot width, heel width and foot length comparisons
Footprint dimensions and stride length data were recorded on the same two subadult male chimpanzees as above, though at a slightly younger age (6.5 and 6.9 years of age, 30.7 and 27.8 kg, respectively). The experimental design is described in detail elsewhere42. In brief, chimpanzees traversed a runway, at the centre of which was a pressure mat (RSScan International) and a container of hydrated sediment in which the chimpanzees could produce footprints. This sediment was taken directly from a layer that preserves 1.5 Ma hominin footprints near Ileret, Kenya50. Laterally positioned video cameras were used to record the chimpanzees as they walked along this trackway and produced footprints. Two digitization softwares, MaxTRAQ Lite+ (v. 18.104.22.168) (Innovisions Systems) and ImageJ v.1.4751, were used to quantify various aspects of their gaits, including stride length. Tape measures and digital callipers were used to directly measure the external dimensions of each chimpanzee’s feet. Scaled photographs were taken of the footprints produced in each trial, and these were later measured using ImageJ software.
Forefoot width, width of digits 1 and 2, divergence ratio, and foot length comparisons
Data were collected by E.J.M. at the Ngamba Island Chimpanzee sanctuary (Entebbe, Uganda) managed by the Chimpanzee Sanctuary and Wildlife Conservation Trust (CSWCT) using procedures approved by the Dartmouth College IACUC. The Tekscan plantar pressure mat (PPM) was positioned within a walkway connecting the overnight enclosure to the open forest habitat, near a gate and underneath a solid cross section to help prevent individuals from jumping over the mat using the ceiling bars. This location was determined using the expertise of the sanctuary keepers. The animals were first introduced to a mat shell that was lacking the internal sensors, to habituate them to the novel stimulus. All subsequent data were collected using both the empty and real PPMs, positioned such that they covered the entire width of the walkway to force individuals to walk across one of the two mats. Both mats were covered with thin green sacks to help disguise them from the chimpanzees and facilitate faster removal if necessary. It was determined that the southeast facing direction was the preferred path for the chimpanzees and the sensor-containing PPM was always positioned there from the second collection onwards. Data were collected twice a day; once in the morning (between 06:45 and 08:00) when the chimpanzees were headed to the forest for their first feeding, and once at 18:00, when the chimpanzees were headed into the overnight enclosure to sleep and receive their last feeding. Data were collected on 46 adult chimpanzees (18 male, 28 female, ages 12–36 years). A subset of 54 dynamic pressure records was analysed. Using the associated Tekscan PPM software, Footmat Research (v. 7.10), the pressure recordings were analysed to determine foot length, forefoot width, the width digits 1 and 2, and the linear distance between the centre of digits 1 and 2. The divergence ratio was calculated by dividing the distance between digits 1 and 2 by the individual’s foot length.
Data were extracted from previous studies of two modern human populations in order to collect all the relevant foot, footprint and gait metrics.
Stride width and step length comparisons
Data were taken on 654 participants, recruited through the Living Laboratory at the Boston Museum of Science19. Sample size was determined by museum visitor traffic and willingness to participate in a scientific study. In brief, this dataset included 73 children between the ages of 2 and 7 years old (29 female and 44 male) and 581 individuals (366 female and 215 male) between the ages of 8 and 80 years. A pressure-sensitive gait carpet (6.1 m long × 0.89 m wide) with a spatial resolution of 1.27 cm and collecting data at 120 Hz (GAITRite) was used to collect stride length and stride width. For a subset of 33 adults, additional data were collected using a Tekscan PPM and analysed with FootMat Research (v. 7.10) to calculate foot length, the width of digits 1 and 2, and the linear distance between the centre of digits 1 and 2. These measurements were used to calculate a divergence ratio as described above in ‘P. troglodytes’.
Forefoot width, heel width and foot length comparisons
Footprint dimensions and stride length data for 29 Daasanach adults (15 male and 14 female, ages 18–47) and 12 children (10 male and 2 female, ages 4–15), who live near the town of Ileret, Kenya and grew up either habitually unshod or minimally shod were taken from Hatala et al.20,21. Details of the experimental protocol largely mirrored the procedures described above. In brief, subjects generated footprints while walking through a rehydrated sample of the same sediments that preserve 1.5 Ma hominin tracks near Ileret. Video cameras were used to record subjects as they produced footprints, and two digitization software packages (MaxTRAQ Lite+ v. 22.214.171.124 and ImageJ v.1.47) were used to measure stride lengths and other kinematic variables. The external dimensions of subjects’ feet were directly measured with tape measures and digital callipers. Scaled photographs of the footprints produced in each trial were measured using ImageJ.
Human cross-stepping footprint experiments
Experiments were carried out by K.G.H. and E.M.W.-H. to investigate whether and how cross-stepping kinematics influence the perimeter dimensions and internal topologies of an individual’s footprints. We could thereby evaluate whether the size and shape of the Laetoli site A tracks could have been generated by a hominin with feet similar to those who left tracks at sites G and S, but while cross-stepping. Detailed methods are provided in Supplementary Information. In brief, ten adult subjects (including six female, three male, and one non-binary between 19 and 52 years old) each completed ten trials in which they produced tracks in sedimentary conditions meant to mimic those at Laetoli37,52. Sample size was determined by availability and willingness to participate in the study. Five trials were completed with a normal, self-selected walking gait and another five were completed with a cross-stepping gait, as inferred for the Laetoli site A trackmaker. In each trial, a focal footprint was selected, measured in situ, and photographed (25–30 photos per footprint). The lengths and widths of the steps bracketing the track were also measured. Photographs were used to generate 3D models of the tracks using Agisoft Metashape software (v.1.7.3), and average normal and cross-stepping tracks were generated for each subject using DigTrace Pro (v.1.8.1)53. Lengths and widths of these averaged tracks were measured using Geomagic Wrap (v. 2021.0.0) (3D Systems). Regional depths were measured and evaluated using the same methods described below (‘Comparative analyses of Laetoli footprint shapes’). Within-subject comparisons enabled us to understand how cross-stepping influenced the dimensions of the perimeter and the internal topology of a subject’s footprints.
Fossil footprint data and analysis
Comparative metrics were quantified from a set of modern human footprints from the Late Pleistocene at Engare Sero, Tanzania. These footprints are an important comparison with the Laetoli footprints, as they were generated in a similar circumstance (footprints in volcanic ash) and represent an early population of unshod modern humans.
A scaled 3D orthophoto of the Engare Sero site was created via photogrammetry by B.Z. and C.L.-P. to visualize the distribution of footprint trackways across the entire site using Agisoft Photoscan (now Agisoft Metashape v. 1.4.4). The model was created from hundreds of photos originally taken by the Smithsonian 3D Digitization Program in 2010. Measurements that were defined in Tuttle4, were taken from the fossil tracks using the software, ImageJ (v. 1.49), and included foot length, forefoot width, heel width and step width of each footprint at Engare Sero. In some cases, partial footprints were included for measurement, as long as they included the requisite landmarks for those measurements. Overall, data were collected from 151 footprints at the Engare Sero site. Of the 151 footprints, 61 footprints were considered partial footprints and 90 footprints were considered complete footprints. From these, 67 step length and stride width measurements and 105 heel width and ball width measurements were included in our analyses.
All measurements for Laetoli trackways G and S were obtained from published sources4,32,42. Box and whisker plots and bivariate graphs (using ggplot254) were generated using R (v. 3.6.1), while the table and pie chart were generated using Microsoft Excel (v. 2102).
Comparative analyses of Laetoli footprint shapes
Comparative analyses followed methods similar to resampling analyses published previously42. In brief, the human comparative sample included 245 footprints produced by 29 adult and 12 juvenile habitually unshod Daasanach individuals traveling at walking speeds. The chimpanzee comparative sample included 45 footprints produced by two individuals walking bipedally. Laetoli samples included only the best-preserved tracks from each site, leaving samples of five footprints from site G that were described by their original excavators as free from taphonomic damage that would obscure track topology (G1-25, G1-27, G1-33, G1-34 and G1-35), and two from site S (L8-S1-2 and L8-S1-4). For site A, we included tracks A2 and A3, as these were the only two for which we were relatively confident in identifying regions of interest across the entire track. Larger sample sizes would be desirable, but we did not want to sacrifice data quality for quantity by including tracks that were overprinted or that did not appear to represent complete foot anatomy. We did not rely on parametric statistical tests for which larger sample sizes would be a necessity, and instead used an analytical approach that could handle smaller sets of observations (see below).
For each experimental and fossil footprint, 3D models were constructed using photogrammetry, through a variety of methods described here for Laetoli site A and elsewhere by the authors for other samples20,21,35,42. Using Geomagic Wrap (v. 2021.0.0) (3D Systems), a best-fit plane was fit to the undisturbed substrate surrounding each track, and this was fixed to the xy plane in world coordinate space. In this orientation, depths of the footprint were measured in the regions of the medial and lateral heel, medial and lateral midfoot, and all five metatarsal heads and toes. Raw depth measurements were normalized, within each footprint, to a scale of 0 to 1 in order to compare the topologies of footprints that may vary in depth. However, a Wilcoxon signed-rank test showed that, overall, human and Laetoli track samples did not differ significantly in their depths (P = 0.08). Within-subject means of the 14 normalized depth measurements were calculated, and a between-subject covariance matrix was created using the subject averages for normalized depths at each of the 14 measured regions. An overall ‘human mean footprint’ was also computed by averaging the within-subject mean normalized depths, and this represented a measure of central tendency as described below.
To represent the range of observed variation in human footprint topography, for 1,000 iterations we randomly sampled a human subject and drew a sample of two of their footprints. We then averaged the normalized depths of those two footprints and computed the Mahalanobis distance (using the between-subject covariance matrix) between this track and the mean of all other subjects’ footprints. Also, for 1,000 iterations we selected a random chimpanzee subject, drew a random sample of two of their footprints and computed the Mahalanobis distance between the average of those tracks and the overall mean human footprint. For the Laetoli tracks, site A and site S samples only included two tracks, so these were simply averaged and the Mahalanobis distance was calculated between each averaged track and the mean human footprint. For Laetoli site G, all possible two-track combinations (ten) were drawn from the sample described above, and the Mahalanobis distance was calculated between the averaged track from each combination and the human mean. In all cases, we calculated multivariate distances using the human between-subject covariance matrix (that is, treating the chimpanzee and fossil tracks as if they came from different human subjects). All analyses described above, and the histogramdisplaying multivariate distances (Fig. 2), were generated using R (v. 3.6.1), with custom scripts and functions from the dplyr55, ggplot254 and reshape256 packages.
While casts of the site A bipedal footprints existed at one point, all our attempts to locate them (see Acknowledgements for a complete list) were unsuccessful. Prior to our fieldwork at Laetoli in 2019, we modelled the original trackway photogrammetrically using extant photography from the site. Original photography of Laetoli site A was taken by J.R. We obtained his photographs of trackway A through Science Photo Library. All photographs were taken with a Nikon F2 on 35-mm Kodachrome slide film. Digital scans from these slides were used to produce a 3D model of the Laetoli A footprints. Unfortunately, since the images were taken in 1977, they were not recorded with modern photogrammetry processing in mind. Several features of the digitized images limit successful and accurate construction of a 3D model. First, there are only four images of the footprints. One of these images has noticeably different exposure settings that caused significant alignment problems during processing, and thus was excluded. All images were shot at oblique angles, from a relatively narrow range of camera positions. A yellow string defining the site grid lies over one of the footprints, obscuring part of it, and casting a shadow. The images were all taken relatively early in the day, so there are shadows within each footprint that create strong contrasts. The slides were digitized at 4,000 dpi, but they were not scanned with specialized equipment to guarantee geometric accuracy, and this potentially introduced more sources of distortion.
However, despite the limitations of the images, it was possible to extract 3D data for the Laetoli A footprints. All processing was done in Agisoft Photoscan Pro (v. 1.7.1). The standard processing steps (align photos, build dense cloud, build mesh, build texture) were run to produce a 3D model, though the process had to be done iteratively to remove noise, ensure accurate alignment of the photos, scale the model appropriately using published measurements, add manual tie points, and refine the model. A DEM (digital elevation model) and orthophotograph were exported for further visualization and analysis in ArcGIS (v. 10.6.1). The 3D model was also exported to Autodesk Meshmixer (v. 3.5.474) to create a ‘watertight’ 3D volume that could be 3D printed for further visualization (1977 model is hosted on Morphosource, ID: 000390119). Photogrammetric reconstruction was validated using published measurements of the footprints. It is important to note however, that there were no published measurements for the depths of the footprints and that the internal anatomy of this reconstruction is potentially misleading because of the incomplete excavation of the footprints2,8,12.
A second, more accurate reconstruction was done using photogrammetry from the re-excavated site A bipedal trackway using 57 images taken in June 2019. The images were captured in a systematic manner using a Nikon D7000 camera and Nikon DX AF-S Nikkor 18–105 mm lens. All photos were taken by hand, from an eye level, while walking a series of transects, across the area of interest. Spacing between shots was kept low to ensure a minimum of approximately 65% overlap between adjacent images. All processing was done using Agisoft Photoscan Pro/Metashape Pro (v. 1.7.1). Standard processing steps (for example, as described15,51) were taken to create a 3D model of the A trail. This included photo alignment, manual editing of the sparse cloud to remove points with high ‘reprojection uncertainty’, building a dense cloud, building a mesh, refining the mesh, then building a texture. During processing, images were checked for sharpness using the ‘image quality’ tool and any images with significantly lower quality were removed. The model was scaled to the real-world using scale bars placed across the region of interest. Finally, an orthophotograph as well as a DEM (digital elevation model) were exported as geotiffs into ArcGIS in an arbitrary local coordinate system for further analysis (2019 model hosted on Morphosource, ID: 000390114).
To generate contour maps, two approaches were used. First, starting with the raw stereolithography scans (.stl file format), Ultimaker Cura software (v.4.8.0) was used to rotate the raw scans and align them with x and y axes. This was a manual process. These rotations were exported to binary-format .stl files. The rotated files were then run through an R script using R version 4.0.3. The R script uses the tidyverse and rgl libraries to load the .stl files into R-friendly dataframes and plot them as contours using ggplot’s geom_contour function. The script is available through GitHub.
Using a second approach, the .stl files were brought into Cloud Compare (v. 2.11.3) to check model orientation. If necessary, models were reoriented to allow the local ground surface to be level using the "level" tool, and then the files were exported. The correctly oriented model was imported into SAGA GIS using the import stereo lithograph file (STL) tool. This tool converts the .stl directly to a DEM raster. The rasters were checked in SAGA and a hillshade generated with the analytic hillshading function using the standard sun position setting of 315° azimuth and 45° height. Both the DEM and hillshade were then exported as geotiffs. These geotiffs were imported into ArcGIS for visualization. The DEM was colored using a red-blue colour ramp to indicate relative depth and this was layered onto the hillshade raster using the NAGI fusion method57 (Extended Data Fig. 8). Cloud compare was used to quantify erosive alterations to the site A footprints from 1977 to 2019.
3-D surface scanning
Three-dimensional surface scans of Laetoli A and plaster casts of bear prints were collected using a Creaform Go!Scan 50.
Further information on research design is available in the Nature Research Reporting Summary linked to this paper.
Previously published data were obtained from refs. 4,19,20,21,28,32,42. All other data supporting the findings of this study are available within the paper and its supplementary information files. The photogrammetric reconstruction of the Laetoli A trackway based on three original photographs from the 1977 expedition is available on Morphosource (https://www.morphosource.org; ID: 000390119). The photogrammetric reconstruction of Laetoli A trackway using 57 photographs taken of the re-excavated Laetoli site A footprints in 2019 is available on Morphosource (ID: 000390114). Source data are provided with this paper.
Leakey, M. Pliocene footprints at Laetoli, northern Tanzania. Antiquity 52, 133 (1978).
Leakey, M. D. & Hay, R. L. Pliocene footprints in the Laetoli Beds at Laetoli, northern Tanzania. Nature 278, 317–323 (1979).
Leakey, M. D. & Harris, J. M. (eds) Laetoli, a Pliocene Site in Northern Tanzania (Clarendon, 1987).
Tuttle, R. H. in Laetoli: A Pliocene Site in Northern Tanzania (eds Leakey, M. D. & Harris, J. M.) 503–523 (Clarendon, 1987).
Day, M. H. in Origine(s) de la Bipedie Chez les Hominides (eds Coppens Y. & Senut B.) 199–213 (Editions du CNRS, 1991).
Leakey, M. Disclosing the Past: An Autobiography (Doubleday, 1984).
Leakey, M. D. Footprints in the ashes of time. Nat. Geo. 155, 446–457 (1979).
White, T. D. & Suwa, G. Hominid footprints at Laetoli: facts and interpretations. Am. J. Phys. Anthropol. 72, 485–514 (1987).
Tuttle, R. H. Bear facts and Laetoli impressions. Am. J. Phys. Anthropol. 63, 230–230 (1984).
Tuttle, R. H. in Hominid Evolution: Past, Present, and Future 129-133 (Alan R. Liss, 1985).
Tuttle, R. H. The pitted pattern of Laetoli feet. J. Nat. Hist. 99, 60–65 (1990).
Tuttle, R., Webb, D. & Tuttle, N. in Origine(s) de la Bipedie Chez les Hominides (eds Coppens Y. & Senut B.) 187–198 (Editions du CNRS, 1991).
Cohen, A., Lockley, M., Halfpenny, J. & Michel, A. E. Modern vertebrate track taphonomy at Lake Manyara, Tanzania. Palaios 6, 371–389 (1991).
Roach, N. T. et al. Pleistocene footprints show intensive use of lake margin habitats by Homo erectus groups. Sci Rep. 6, 26374 (2016).
Zimmer, B. et al. Using differential structure-from-motion photogrammetry to quantify erosion at the Engare Sero footprint site, Tanzania. Quat. Sci. Rev. 198, 226–241 (2018).
Su, D. F. & Harrison, T. Ecological implications of the relative rarity of fossil hominins at Laetoli. J. Hum. Evol. 55, 672–681 (2008).
Harrison, T. in Paleontology and Geology of Laetoli: Human Evolution in Context 1–14 (Springer, 2011).
Roach, N. T. et al. Pleistocene animal communities of a 1.5 million-year-old lake margin grassland and their relationship to Homo erectus paleoecology. J. Hum. Evol. 122, 70–83 (2018).
DeSilva, J. M. & Gill, S. V. Brief communication: a midtarsal (midfoot) break in the human foot. Am. J. Phys. Anthropol.151, 495–499 (2013).
Hatala, K. G., Dingwall, H. L., Wunderlich, R. E. & Richmond, B. G. The relationship between plantar pressure and footprint shape. J. Hum. Evol. 65, 21–28 (2013).
Hatala, K. G., Wunderlich, R. E., Dingwall, H. L. & Richmond, B. G. Interpreting locomotor biomechanics from the morphology of human footprints. J. Hum. Evol. 90, 38–48 (2016).
Liutkus-Pierce, C. M. et al. Radioisotopic age, formation, and preservation of Late Pleistocene human footprints at Engare Sero, Tanzania. Palaeogeogr. Palaeoclimatol. Palaeoecol. 463, 68–82 (2016).
Hatala, K. G. et al. Snapshots of human anatomy, locomotion, and behavior from Late Pleistocene footprints at Engare Sero, Tanzania. Sci. Rep. 10, 7740 (2020).
Cham, R. & Redfern, M. S. Changes in gait when anticipating slippery floors. Gait Posture 15, 159–171 (2002).
Fukushima, T. Angle and distance between steps. J. Bone. Jt. Surg. 37, 1311 (1955).
Murray, M. P., Drought, A. B. & Kory, R. C. Walking patterns of normal men. J. Bone Jt. Surg. 46, 335–360 (1964).
Maki, B. E. & McIlroy, W. E. Control of rapid limb movements for balance recovery: age-related changes and implications for fall prevention. Age Ageing 35, ii12–ii18 (2006).
Thompson, N. E., O’Neill, M. C., Holowka, N. B. & Demes, B. Step width and frontal plane trunk motion in bipedal chimpanzee and human walking. J. Hum. Evol. 125, 27–37 (2018).
O’Neill, M. C., Demes, B., Thompson, N. E. & Umberger, B. R. Three-dimensional kinematics and the origin of the hominin walking stride. J. R. Soc. Interface 15, 20180205 (2018).
Tuttle, R. H. Evolution of hominid bipedalism and prehensile capabilities. Philos. Trans. R. Soc. Lond. B. 292, 89–94 (1981).
Harcourt-Smith, W. E. Did Australopithecus afarensis make the Laetoli footprint trail?—New insights into an old problem. Am. J. Phys. Anthropol. S40, 116 (2005).
Pelissero, A. J. A Comparative Analysis of Newly Discovered Pliocene Hominin Footprints from Laetoli, Tanzania (Univ. Colorado at Denver, 2017).
Haile-Selassie, Y. et al. A new hominin foot from Ethiopia shows multiple Pliocene bipedal adaptations. Nature 483, 565–569 (2012).
Dingwall, H. L., Hatala, K. G., Wunderlich, R. E. & Richmond, B. G. Hominin stature, body mass, and walking speed estimates based on 1.5 million-year-old fossil footprints at Ileret, Kenya. J. Hum. Evol. 64, 556–568 (2013).
Masao, F. T. et al. New footprints from Laetoli (Tanzania) provide evidence for marked body size variation in early hominins. eLife 5, e19568 (2016).
DeSilva, J. M., Gill, C. M., Prang, T. C., Bredella, M. A. & Alemseged, Z. A nearly complete foot from Dikika, Ethiopia and its implications for the ontogeny and function of Australopithecus afarensis. Sci. Adv. 4, eaar7723 (2018).
Raichlen, D. A. & Gordon, A. D. Interpretation of footprints from Site S confirms human-like bipedal biomechanics in Laetoli hominins. J. Hum. Evol. 107, 134–138 (2017).
Bennett, M. R. & Morse, S. A. in Human Footprints: Fossilised Locomotion? 101–136 (Springer, 2014).
Crompton, R. H. et al. Human-like external function of the foot, and fully upright gait, confirmed in the 3.66 million year old Laetoli hominin footprints by topographic statistics, experimental footprint-formation and computer simulation. J. R. Soc. Interface 9, 707–719 (2012).
Meldrum, D. J., Lockley, M. G., Lucas, S. G. & Musiba, C. Ichnotaxonomy of the Laetoli trackways: the earliest hominin footprints. J. Afr. Earth. Sci. 60, 1–12 (2011).
Ward, C. V., Kimbel, W. H. & Johanson, D. C. Complete fourth metatarsal and arches in the foot of Australopithecus afarensis. Science 331, 750–753 (2011).
Hatala, K. G., Demes, B. & Richmond, B. G. Laetoli footprints reveal bipedal gait biomechanics different from those of modern humans and chimpanzees. Proc. R. Soc. Lond. B 283, 20160235 (2016).
Leakey, M. G. et al. New hominin genus from eastern Africa shows diverse middle Pliocene lineages. Nature 410, 433–440 (2001).
Haile-Selassie, Y., et al New species from Ethiopia further expands Middle Pliocene hominin diversity. Nature 521, 483–488 (2015).
Musiba, C., et al Newly discovered hominin remains from upper Laetoli beds in northern Tanzania. Abstracts of the PaleoAnthropology Society, 2010 Meetings. PaleoAnthropology 2010, A0001–A0040 (2010).
Pelissero, A. J. et al. Photogrammetry imaging: a fresh look at the Laetoli hominin footprints in relation to recent discoveries. Am. J. Phys. Anthropol. 162, 312 (2017).
Pelissero, A., Musiba, C., Magori, C., Mwankunda, J. & Bunn, H. Rethinking the Laetoli hominin trackmakers in light of new prints at Site S. In Paleoanthropology Society Meeting, Albuquerque, NM (2019).
DeSilva, J., McNutt, E., Benoit, J. & Zipfel, B. One small step: a review of Plio‐Pleistocene hominin foot evolution. Am. J. Phys. Anthropol. 168, 63–140 (2019).
Musiba, C. M., Mabula, A., Selvaggio, M. & Magori, C. C. Pliocene animal trackways at Laetoli: research and conservation potential. Ichnos 15, 166–178 (2008).
Bennett, M. R. et al. Early hominin foot morphology based on 1.5-million-year-old footprints from Ileret, Kenya. Science 323, 1197–1201 (2009).
Abramoff, M. D., Magalhaes, P. J. & Ram, S. J. Image processing with ImageJ. Biophotonics Int. 11, 36–42 (2004).
D’Aout, K., Meert, L., Van Gheluwe, B., De Clercq, D. & Aerts, P. Experimentally generated footprints in sand: analysis and consequences for the interpretation of fossil and forensic footprints. Am. J. Phys. Anthropol. 141, 515–525 (2010).
Budka, M. et al. DigTrace Pro v.1.8.1 (Bournemouth University, 2016).
Wickham, H. ggplot2: Elegant Graphics for Data Analysis (Springer, 2016).
Wickham, H., François, R., Henry, L. & Müller, K. dplyr: a grammar of data manipulation. Version 0.8.3 (2019).
Wickham, H. Reshape2: flexibly reshape data: a reboot of the Reshape package. Version 1.4.4 (CRAN, 2019).
Nagi, R. Maintaining detail and color definition when integrating color and grayscale rasters using no alteration of grayscale or intensity (NAGI) fusion method. In Proc. 2012 AutoCarto (2012).
We thank R. Tuttle for his mentorship and inspiration; M. Larkin for her help collecting bear footprint data; R. Leakey, B. Wood, H. de Lumley, T. White, R. Crompton, R. Clarke, W. Harcourt-Smith, C. Stringer, H. Bonney and the London Natural History Museum, and J. Kibii and the National Museum of Kenya for assistance as we attempted to track down photographs and casts of the Laetoli A footprints; J. Sappington for photographic support; and V. Rossi and A. Metallo for help with 3D visualization; the Director General of Tanzania Commission for Science and Technology (COSTECH) for granting our team the COSTECH Research Permits (2019-370- NA-2019-2016); F. Manongi, J. Mwankunda and M. Mwambungu for allowing us to camp and work at Laetoli. Funding for this research was provided by the National Geographic (8748-10), Leakey Foundation (71483-001), National Science Foundation (BCS-1128170, DGE-080163, BCE-1730822, GRFP (No. 1840344), the Smithsonian Institution’s Human Origins Program, the Evolving Earth Foundation, the Explorers Club, and the Claire Garber Goodman Fund-Dartmouth College.
The authors declare no competing interests.
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Extended data figures and tables
Photographs were taken by J. Reader (left: 1977) and J. DeSilva (right: 2019) at similar overhead angles and times of day (see similarities in shadows cast across the print). Notice the removed matrix infill in the hallucial impression and the presence of the previously unseen second digit impression in 2019 image. Below: comparisons of the photogrammetric meshes of a pothole and footprints A2 and A3 using Cloud Compare15. The impact of erosion on the morphology of the footprints was assessed by quantifying changes to an oval depression located west of A3. Notice that significant changes occurred around the rim of the depression, as would be expected through erosion, that are absent around the rims of the A2 and A3. Instead, significant differences between A2 and A3 are located internally and are a result of a more thorough excavation of the prints.
Left image shows original 3D scan. Right image highlights the proposed impressions for the toes (blue circles) and matrix infill (green), as well as the potential evidence for midfoot mobility (red).
Extended Data Fig. 3 Incidence of bipedalism in Ursus americanus and Examples of kinematic data collection.
(top) Pie charts showing the frequency of bipedal behaviors in wild Ursus americanus. The blue chart represents the time spent independently bipedal (locomotor or postural) out of the total 50.9 h in which bear behavior was observed. The orange chart represents the breakdown of time spent independently bipedal into its postural and locomotor (i.e., bears took one or more steps) components. The green chart represents the frequency of occurrences where bears walked 4 or more steps reflecting a similar circumstance to Laetoli trackway A. (bottom left) Juvenile female walks bipedally, unassisted through mud trackway. (bottom right) Example left footprint from one of the juvenile males.
(a) Forefoot width to step length; (b) heel width to step length; (c) heel width to forefoot width; and (d) stride width to step length. Notice that for foot proportions (c) and stride width (d), Laetoli A is unlike the tracks produced by bears. In (d) the negative value in Laetoli A represents the fact that the track is demonstrating cross-stepping. (a-c) Boxplot represents median (center line), upper and lower quartiles (box limits), range (whiskers), and outliers (points) and individual footprints sample sizes for each species are indicated in the figure panels. (a-d) In all plots, n = 1 for all Laetoli trackways, and chimpanzees were traveling bipedally. Data sources match Extended Data Table 1.
(a) Ratio between toe impression dimensions across footprints from the comparative species and Laetoli A3. Values in blue=the ratio between the width of the 2nd digit compared to the hallux. Values in orange=ratio between the width of the 4th digit compared to the 5th in Ursus americanus. (Insert image) Comparison between 3-D scan of right ursid footprint (blue) and A3 (orange). Note the large size of the 5th digit impression in ursids but overall shape difference between the ursid track and A3. (b) Ratio of stride width to step length across the different species, including the Laetoli bipedal trackways. Boxplot definitions are as in Extended Data Fig. 4 and individual footprint sample sizes are indicated in the figure panels. In 5a, the chimpanzees were traveling quadrupedally; in 5b, chimpanzees were moving bipedally. Data sources match Extended Data Table 1.
Extended Data Fig. 6 Boxplots showing the divergence ratio between the first digit and 2nd digit across the comparative species and two Laetoli trackways.
Divergence ratio was measured by dividing the linear distance between the midpoint of digits one and two by the foot length. Chimpanzees were traveling quadrupedally and data were obtained from plantar pressure impressions. Boxplot definitions are as in Extended Data Fig. 4 and individual footprint sample sizes are indicated in the figure panel. Data sources match Extended Data Table 1. We attempted to measure hallucial divergence following Bennett et al50. but were stymied by matrix obscuring the deepest region of the ball of the foot.
Extended Data Fig. 7 Histogram of Mahalanobis distances between the mean unshod human footprint and resampled unshod human footprints (gray) and chimpanzee footprints (yellow).
As in Figure 3c, blue, orange, and green dashed lines represent samples from Laetoli G1, S1, and A, respectively. Only Laetoli A is labeled, for clarity. Sample sizes for these samples as in Fig. 2c as well. The black dotted-dashed lines have been added to represent the average cross-stepping footprints produced by 10 adult habitually shod humans. All fall squarely within the distribution of unshod human footprints (probabilities of sampling tracks like these range from 0.20 to 0.94), and a great distance apart from the Laetoli A sample (green). Human cross-stepping footprints tended to be slightly closer to the human mean than the Laetoli S1 and G1 samples, but their distribution does overlap with the Laetoli S1 sample and with some of the Laetoli G1 samples. Cross-stepping footprints fell, on average, a Mahalanobis distance of 27.2 farther from the human mean than their “normal” walking counterpart.
Left panel: Complete scan of Laetoli A trackway with A1 at the bottom and A5 at the top. Right side: Zoomed in images of the individual footprints and their corresponding contour images.
About this article
Cite this article
McNutt, E.J., Hatala, K.G., Miller, C. et al. Footprint evidence of early hominin locomotor diversity at Laetoli, Tanzania. Nature 600, 468–471 (2021). https://doi.org/10.1038/s41586-021-04187-7
This article is cited by
Nature Ecology & Evolution (2023)