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Perikymata and linear hypoplastic defect depths by tooth type. Neanderthals have significantly shallower perikymata (n = 280; 150 H. sapiens and 130 Neanderthal) and defects (n = 71; 35 H. sapiens and 36 Neanderthal) than H. sapiens. Inter-and intra-individual comparisons suggest that faster-growing and thinnerenameled teeth (i.e., Neanderthals compared to H. sapiens; incisors compared to canines) have shallower perikymata and defects at the population level. LLI1/ULI1 = lower/upper central incisor; LLI2/ULI2 = lower/ upper lateral incisor; LC = lower/upper canine. Figure generated in RStudio (version 1.3.959) 50 .

Perikymata and linear hypoplastic defect depths by tooth type. Neanderthals have significantly shallower perikymata (n = 280; 150 H. sapiens and 130 Neanderthal) and defects (n = 71; 35 H. sapiens and 36 Neanderthal) than H. sapiens. Inter-and intra-individual comparisons suggest that faster-growing and thinnerenameled teeth (i.e., Neanderthals compared to H. sapiens; incisors compared to canines) have shallower perikymata and defects at the population level. LLI1/ULI1 = lower/upper central incisor; LLI2/ULI2 = lower/ upper lateral incisor; LC = lower/upper canine. Figure generated in RStudio (version 1.3.959) 50 .

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Early life stress disrupts growth and creates horizontal grooves on the tooth surface in humans and other mammals, yet there is no consensus for their quantitative analysis. Linear defects are considered to be nonspecific stress indicators, but evidence suggests that intermittent, severe stressors create deeper defects than chronic, low-level stres...

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... Neanderthal sample has significantly shallower perikymata than the H. sapiens sample (F(1,12) = 27.8, p < 0.001) (Fig. 2). The H. sapiens sample has perikymata that are an average of 2.33 times (range 1.69-3.65) deeper than the Neanderthal sample in incisors, and 3.24 times (range 3.05-3.65) deeper in canines. Perikymata depths range from shallowest in the La Chaise Neanderthal upper canines and incisors to the deepest in the Çatalhöyük lower canines and ...
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... Neanderthal sample also has significantly shallower LEH defects than H. sapiens (F(1,16) = 30.0, p < 0.001) (Fig. 2). Defect depths follow a similar pattern with La Chaise Neanderthal upper incisors having the shallowest defects and H. sapiens lower canines from the Saxon burials at Hildesheim and Çatalhöyük having the deepest defects. However, there are no significant differences in LEH severity ratios between Neanderthals and H. sapiens, as ...
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... ( To test the effect of leveling algorithms that have been used in other studies to remove the effect of curvature 15,20 , and ultimately move toward a methodological consensus for measuring defect depth, plane and sphere-type form removal algorithms (within SensoSCAN) were applied to two digital elevation models (DEMs) from Le Moustier canines (Fig. S2). Leveled values underestimate the depth of defects, being on average 24.3% shallower than raw depths (range = 16.1-27.9%; N = 4), and with a mean absolute difference of 9.9 µm (range = 6.9-11.1 µm; N = 4). When the same algorithms are applied to perikymata, they have the opposite effect, making perikymata appear artificially deeper. ...
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... to earlier hominins Australopithecus africanus (26.0 µm) and H. naledi (26.9 µm) as reported by Skinner 21 , as well as nonhuman apes (23.6 µm in mountain gorillas). However, the A. africanus and H. naledi depths 21 were collected from leveled DEMs and therefore likely underestimate the true depth, based on our comparisons of leveled vs. raw data (Fig. S2). In terms of differences among the H. sapiens samples, relatively little is known about enamel growth variation within our species. A histological analysis of contemporary European and South Africans 37 , and the variation in the timing of dental eruption 38 , suggest that considerable variation can be expected. ...

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... However, that study did not adequately control for enamel surface abrasion, which can wear away minor defects, and relied on observations made with a 10× hand lens. Newer protocols for LEH observation emphasize the exclusion of teeth with abraded enamel surfaces and utilize improved imaging techniques (e.g., Guatelli-Steinberg, Ferrell, and Spence 2012;McGrath et al. 2018McGrath et al. , 2021. These methodological advances make it worthwhile to reexamine the transfer question. ...
... Depending upon where measurements were taken in relation to perikymata, the most minor defects are likely to have been missed, but the threshold for detection is the same overall enamel surfaces examined. McGrath et al. (2021) used a confocal profilometer to measure defect depth factoring out underlying surface curvature. Measurements of defect depths were not analyzed here as the measuring microscope's software (VisionGauge; Visionx ...
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... Modern scientific and commercial technological advancements necessitate nanometer-resolution surface topography over a broad dynamic range. With the growing demand for miniaturized devices such as nano/micro electromechanical systems (NEMS and MEMS) [1,2], nanostructured optical interfaces [3], and micro-fluidic chips [4], economical and convenient two and three-dimensional surface profilometry has gained popularity, allowing for roughness estimation [5], morphological analysis [6,7] film thickness measurement [8,9] and structural assessment of integrated devices [10,11]. Electrical profilometry maps micron-sized surface characteristics using sensitive impedance-based probing methods [12,13], whose performance is substrate dependent and incurs non-linearity. ...
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... They reveal that the probability for any single tooth to manifest a hypoplastic defect (of any form) is similar in Neanderthals and UPMH. These results support previous work arguing for the lack of substantial differences in overall childhood stress levels between the two hominin groups [8][9][10] . Our findings therefore counter arguments that Neanderthal lives were generally much more stressful compared to those of UPMH. ...
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... Their behavioral repertoire was thought to have provided UPMH with a competitive advantage over Neanderthals, allowing them to persist while Neanderthals perished [3][4][5][6][7][8][9]. Some recent studies, however, are casting doubt on this view, arguing instead that Neanderthals and UPMH led similarly stressful lives [10][11][12]. ...
... Thus, enamel hypoplasia, especially in its linear form (LEH), is considered a well-established marker of non-speci c physiological stress experienced during ontogeny [13][14][15]23]. The potential of using enamel growth disruptions to elucidate stress pro les of past populations has prompted many studies to track enamel hypoplasia occurrences in Paleolithic hominins [12,[24][25][26][27][28][29][30][31][32]. However, these have provided contradictory results when it comes to reconstructions and comparisons of stress levels in Neanderthals and UPMH. ...
... They reveal that the probability for any single tooth to manifest a hypoplastic defect (of any form) is similar in Neanderthals and UPMH. These results support previous work arguing for the lack of substantial differences in overall childhood stress levels between the two hominin groups [12,20,21,35]. Our ndings therefore counter arguments that Neanderthal lives were generally much more stressful compared to those of UPMH. ...
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... One condition that has long served as a marker of metabolic or systemic perturbation in bioarchaeology and paleoanthropology is enamel hypoplasia. This work persists today, albeit with methodological advances and refined interpretive paradigms (e.g., Elcock et al., 2006;Ham et al., 2021;McGrath et al., 2021;Towle & Irish, 2020). ...
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... This is because defect margins are not always well-defined due to the curvature of the tooth and differences in perikymata widths within a defect (Hillson & Bond, 1997). Research using enamel depth profiles and/or micro-CT imaging may remedy the issue of subjective defect and duration identification (e.g., Cares Henriquez & Oxenham, 2020;McGrath et al., 2021;Xing et al., 2016). However, such methodology is associated with its own set of limitations because it requires specialized equipment that cannot usually be applied to larger bioarchaeological samples required for studies of FA, caused by restrictions from data collection and travel. ...
Article
Objectives Recent tests of the relationship between enamel defects, an indicator of early life stress, and fluctuating asymmetry (FA), a measure of cumulative developmental instability, have produced equivocal results. This may be because they use methods that underestimate the number of defects. We reinvestigate this relationship using high‐resolution microscopy images of tooth surfaces. Further, we test the hypothesis that developmental stresses during the earliest period of tooth development have a greater impact on FA than stresses during subsequent periods. Materials and Methods The sample consists of 48 individuals from two colonial‐era cemeteries in Mexico City. Using one canine from each individual, we created photomontages using a 2D light microscope. Tooth crowns were divided into three developmental periods. Defects were identified as widely spaced perikymata using moving z‐scores. We compared defect presence, frequency, and timing to FA calculated from 11 landmarks using geometric morphometrics from 3D models of each cranium. Results Both the presence and frequency of enamel defects are significantly associated with an increase in FA. Contrary to our expectations, defects that formed in the latest developmental period (4–5.5 years) were uniquely associated with an increase in FA, relative to the other two periods. Discussion The presence and frequency of stress during childhood increases developmental instability. The time between 4 and 5.5 years may be a sensitive window of development in which disruptions to growth have a long‐lasting effect on developmental instability. Results indicate that research on developmental stress should consider the timing and frequency of stress events to more fully understand their impact on later life.
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Chapter
Despite a remarkably persistent pop culture image of Neanderthals as semi-upright, hairy, cavemen wielding clubs, science provides us with a different picture. There is no doubt that the evolutionary forces that shaped Neanderthals and Homo sapiens differed, but recent evidence of interbreeding tells us that our anatomy and physiology were compatible and differences in physical appearance were not an obstacle to social interaction. Similarities in growth and development indicate that, like us, Neanderthals also gave birth to helpless young, and imply complex social lives necessary to support reproduction and protracted phases of offspring development. Of course, some uncertainty will always surround the behaviors of extinct species, but we can be sure that Neanderthals had sex and successfully reproduced for hundreds of thousands of years, and the archeological record and DNA evidence can illuminate behaviors that are invisible anatomically. In this chapter, we synthesize diverse data, theories, and models to reconsider aspects of Neanderthal sexual and reproductive behavior, and contextualize inferences within our current understanding of their physical characteristics, life-ways, and genomics.
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... A short postnatal enamel formation period has been reported for a deciduous incisor of the Fumane 2 upper Palaeolithic modern human infant (39-42 ka) [29], which differs from longer enamel growth periods reported for extant humans [37]. Relatively rapid formation rates have also been reported for Neanderthal permanent anterior teeth [21,47]. ...