Introduction

A fundamental goal in psychology and neuroscience is to understand the complex relationship between brain structure and brain function, as well as how that relationship provides a scaffold for efficient cognition and behavior. Of all the neuroanatomical features to target, recent work shows that morphological features of hominoid-specific, shallow indentations, or sulci, of the cerebral cortex are not only functionally and cognitively meaningful, but also are particularly impacted by multiple brain-related disorders and aging (Amiez et al., 2019, 2018; Ammons et al., 2021; Cachia et al., 2021; Fornito et al., 2004; Garrison et al., 2015; Harper et al., 2022; Hathaway et al., 2023; Lopez-Persem et al., 2019; Miller et al., 2021, 2020; Nakamura et al., 2020; Parker et al., 2023; Voorhies et al., 2021; Weiner, 2019; Willbrand et al., 2023b, 2023c, 2022a, 2022b; Yao et al., 2022). The combination of these findings provides growing support for a classic theory proposing that the late emergence of these structures in gestation within association cortices, as well as their prolonged development, may co-occur with specific functional and microstructural features that could support specific cognitive abilities that also have a protracted development (Sanides, 1964). Nevertheless, despite the developmental, evolutionary, functional, cognitive, and theoretical relevance of these findings, they have mainly been restricted to only a subset of association cortices such as the prefrontal, cingulate, and ventral occipitotemporal cortices (Amiez et al., 2019, 2018; Ammons et al., 2021; Cachia et al., 2021; Fornito et al., 2004; Garrison et al., 2015; Harper et al., 2022; Hathaway et al., 2023; Lopez-Persem et al., 2019; Miller et al., 2021, 2020; Nakamura et al., 2020; Parker et al., 2023; Voorhies et al., 2021; Weiner, 2019; Willbrand et al., 2023b, 2023c, 2022a, 2022b; Yao et al., 2022). Thus, examining the relationship among these structures (also known as tertiary sulci) relative to architectonic and functional features of the cerebral cortex, as well as relative to cognition, remains uncharted in other association cortices such as the lateral parietal cortex (LPC).

As LPC is a cortical extent that has expanded extensively throughout evolution (Van Essen et al., 2018; Zilles et al., 2013), there is great interest in the structure and function of LPC in development, aging, across species, and in different patient populations. Yet, key gaps in knowledge relating individual differences in the structure of LPC to individual differences in the functional organization of LPC and cognitive performance remain for at least four main reasons. First, one line of recent work shows that LPC displays a much more complex sulcal patterning than previously thought (Drudik et al., 2022; Petrides, 2019; Segal and Petrides, 2012; Zlatkina and Petrides, 2014), while a second line of work shows that LPC is tiled with many maps and discrete functional regions spanning modalities and functions such as vision, memory, attention, action, haptics, and multisensory integration in addition to theory of mind, cognitive control, and subdivisions of the default mode network (Goodale and Milner, 1992; Harvey et al., 2015, 2013; Humphreys and Tibon, 2023; Konen and Kastner, 2008; Mackey et al., 2017; Schurz et al., 2017). Second, a majority of the time, the two lines of work are conducted independently from one another and the majority of human neuroimaging studies of LPC implement group analyses on average brain templates—which causes LPC sulci to disappear (Fig. 1). Third, despite the recently identified complexity of LPC sulcal patterning, recent studies have also uncovered previously overlooked tertiary sulci in association cortices (for example, in the posterior cingulate cortex (Willbrand et al., 2023c, 2022a)). Thus, fourth, it is unknown if additional LPC tertiary sulci are waiting to be discovered and if so, could improve our understanding of the structural-functional organization of LPC with potential cognitive insights as in other association cortices. Critically, while such findings would have developmental, evolutionary, functional, cognitive, and theoretical implications for addressing novel questions in future studies, they would also have translational applications as sulci serve as biomarkers in neurodevelopmental disorders (Ammons et al., 2021; Cachia et al., 2021; Garrison et al., 2015; Nakamura et al., 2020) and “corridors” for neurosurgery (Tomaiuolo et al., 2022; Tomaiuolo and Giordano, 2016).

Fig. 1.

In the present study, we first manually defined LPC sulci in 144 young adult hemispheres using the most recent definitions of LPC sulci (Petrides, 2019). By manually labeling over 2,000 sulci, we uncovered four previously undefined (Supplementary Methods and Supplementary Figs. 1-4 for historical details) sulci in the cortical expanse between the caudal branches of the superior temporal sulcus (cSTS) and two parts of the intraparietal sulcus (IPS)—a cortical expanse recently referenced as containing sensory “bridge” regions of the temporal-parietal-occipital junction (Glasser et al., 2016)—which we term the supralateral occipital sulci (ventral: slocs-v; dorsal: slocs-d) and posterior angular sulci (ventral: pAngs-d; dorsal: pAngs-d). We then utilized morphological (depth and surface area), architectural (gray matter thickness and myelination), and functional (resting-state functional connectivity) data available in each participant to assess whether the most common of these structures (slocs-v) was dissociable from surrounding sulci. Finally, we assessed whether the updated view of the LPC/LPOJ sulcal landscape provided cognitive insights using a model-based, data-driven approach (Voorhies et al., 2021) relating sulcal morphology to behavior on tasks known to activate regions within this cortical expanse (for example, reasoning and spatial orientation (Gur et al., 2000; Karnath, 1997; Vendetti and Bunge, 2014; Wendelken, 2014)).

Results

Four previously undefined small and shallow sulci in the lateral parieto-occipital junction (LPOJ)

In addition to defining the 13 sulci previously described within the LPC/LPOJ, as well as the posterior superior temporal cortex (Methods) (Petrides, 2019) in individual participants, we could also identify as many as four small and shallow sulci situated within the LPC/LPOJ that were more variable across individuals and uncharted until now (Supplementary Methods and Supplementary Figs. 1-4). Macroanatomically, we could identify two sulci between the cSTS3 and the IPS-PO/lTOS ventrally and two sulci between the cSTS2 and the pips/IPS dorsally.

Ventrally, we refer to these sulci as ventral (slocs-v; sulcus 5 in Fig. 1) and dorsal (slocs-d; sulcus 6 in Fig. 1) components of the supralateral occipital sulcus. The slocs-v, located between the posterior cSTS3 and lTOS, was present in 98.6% of hemispheres (left hemisphere: N = 71/72; right hemisphere: N = 71/72; Fig. 1). Conversely, the slocs-d, located between the cSTS3 and IPS-PO, was present 68.0% of the time (left hemisphere: N = 50/72; right hemisphere: N = 48/72; Fig. 1). Dorsally, we refer to the other newly identified sulci as the ventral (pAngs-v; sulcus 7 in Fig. 1) and dorsal (pAngs-d; sulcus 8 in Fig. 1) components of the posterior angular sulcus. The pAng components were more rare than the slocs components. Specifically, pAngs-v, located between cSTS2 and pips, was identifiable 31.3% of the time (19 left and 26 right hemispheres; Fig. 1). Located between cSTS2 and the IPS, pAngs-d was identifiable only 13.2% of the time (8 left and 11 right hemispheres; Fig. 1). Though we characterize these sulci in this paper for the first time, the location of these four sulci is consistent with the presence of variable “accessory sulci” in this cortical expanse mentioned in prior modern and classic studies (Supplementary Methods).

These incidence rates were significantly different (GLM, main effect of sulcus: χ2(3) = 166.53, p < .0001; no hemispheric effects: ps > .68). The slocs-v was more common than the other three sulci (ps < .0001), slocs-d was more common than the pAngs components (ps < .0001), and pAngs-v was more common than pAngs-d (p = .002). We could further identify these sulci in post-mortem hemispheres (Supplementary Figs. 2, 3). Finally, to help guide future research on these newly- and previously-classified LPC/LPOJ sulci, we generated probabilistic maps of each of these 17 sulci and share them with the field with the publication of this paper (Supplementary Fig. 6).

The slocs-v is morphologically, architecturally, and functionally dissociable from nearby sulci

Given that the slocs-v was present in the majority of participants (98.6% across hemispheres), we focused our analyses on this stable sulcal feature of the LPOJ. To do so, we first tested whether the slocs-v was morphologically (depth and surface area) and architecturally (gray matter thickness and myelination) distinct from the two sulci surrounding it: the cSTS3 and lTOS (Fig. 1; Supplementary Fig. 7 for these metrics in all 17 sulci examined). An rm-ANOVA (within-participant factors: sulcus, metric, and hemisphere for standardized metric units) revealed a sulcus x metric interaction (F(4, 276.19) = 179.15, η2 = 0.38, p < .001). Post hoc tests showed four main differences: (i) the slocs-v was shallower than cSTS3 (p < .001) but not lTOS (p = .60), (ii) the slocs-v was smaller than both the cSTS3 and lTOS (ps < .001), (iii) the slocs-v was thicker than both the cSTS3 and lTOS (ps < .001), and iv) the slocs-v was less myelinated than both the cSTS and lTOS (ps < .001; Fig. 2a). There was also a sulcus x metric x hemisphere interaction (F(4.20, 289.81) = 4.16, η2 = 0.01, p = .002; Supplementary Results).

Fig. 2.

We then tested whether the slocs-v was also functionally distinct from the cSTS3 and lTOS by leveraging resting-state network parcellations for each individual participant to quantify “connectivity fingerprints” for each sulcus in each hemisphere of each participant (Methods) (Kong et al., 2019). An rm-ANOVA (within-participant factors: sulcus, network, and hemisphere for Dice coefficient overlap) revealed a sulcus x network interaction (F(32, 2144) = 80.18, η2 = 0.55, p < .001). Post hoc tests showed that this interaction was driven by four effects: (i) the cSTS3 overlapped more with the Default A subnetwork than both the slocs-v and lTOS (ps < .001), (ii) the slocs-v overlapped more with the Default C subnetwork than the lTOS (p < .001) and marginally than the cSTS3 (p = .077), (iii) the slocs-v overlapped more with the Dorsal Attention A subnetwork than both the cSTS3 and lTOS (ps < .001), and iv) the lTOS overlapped more with the Visual A and Visual B subnetworks than both the cSTS3 and slocs-v (ps < .004; Fig. 2b). There was also a sulcus x network x hemisphere interaction (F(32, 2144) = 3.99, η2 = 0.06, p < .001; Supplementary Results). Together, these results indicate that the slocs-v is a morphologically, architecturally, and functionally distinct structure from its sulcal neighbors, and thus, deserves a distinct neuroanatomical definition.

We further found that the three caudal STS rami (Petrides, 2019; Segal and Petrides, 2012) and intermediate parietal sulci (aipsJ and pips) (Petrides, 2019; Zlatkina and Petrides, 2014) are morphologically, architecturally, and functionally distinct structures for the first time (to our knowledge), which empirically supports their distinctions with separate sulcal labels (Supplementary Results and Supplementary Fig. 8).

The morphology of LPC/LPOJ sulci, including the slocs-v, is related to cognitive performance

Finally, leveraging a data-driven approach of cross-validated LASSO feature selection, we sought to determine whether sulcal depth, a main defining feature of sulci, related to cognitive performance (Methods). To do so, we primarily focused on spatial orientation and reasoning given that these abilities recruit multiple subregions of lateral parietal and/or occipital cortices (Gur et al., 2000; Karnath, 1997; Vendetti and Bunge, 2014; Wendelken, 2014). As in prior work (Voorhies et al., 2021; Willbrand et al., 2023b; Yao et al., 2022), we chose the model at the alpha that minimized MSE_cv. Participants with a slocs-v in both hemispheres and all behavioral metrics were included (N = 69). Due to their rarity (being in less than 70% of hemispheres at most), we did not include the slocs-d or pAng components in this analysis.

This method revealed an association between spatial orientation scores and normalized sulcal depth in the left hemisphere (MSE_cv = 25.63, alpha = 0.05; Fig. 3a), but not in the right hemisphere (MSE_cv = 26.41, alpha = 0.3). Further, we found that no LPC/LPOJ sulci were selected for reasoning in either hemisphere (right: alpha = 0.3, MSE = 24.01; left: alpha = 0.3, MSE = 24.01). Six left hemisphere LPC/LPOJ sulci were related to spatial orientation task performance Fig. 3a, b). Four of these sulci were positioned ventrally: cSTS3 (β = −9.77), slocs-v (β = −3.36), lTOS (β = −4.91), and mTOS (β = −0.06), whereas two were positioned dorsally: pips (β = 5.02), and SPS (β = 4.30; Fig. 3a, b). Using LooCV to construct models that predict behavior, the LASSO-selected model explained variation in spatial orientation score (R² = 0.06, MSE_cv = 23.99) above and beyond a model with all left hemisphere sulci (R² < 0.01, MSE_cv = 27.12). This model also showed a moderate correspondence (r_s = 0.29, p = .01; Fig. 3c) between predicted and actual measured scores. We then tested for anatomical and behavioral specificity using the AIC, which revealed two primary findings. First, we found that the LASSO-selected sulcal depth model outperformed a model using the cortical thickness of the six LASSO-selected sulci (R² < .01, MSE = 26.02, AIC – AIC = 2.19). This model also showed task specificity as these sulci outperformed a model with processing speed (R² < .01, MSE = 254.65, AIC – AIC = 63.57). Thus, our data-driven model explains a significant amount of variance on a spatial orientation task and shows behavioral and morphological specificity.

Fig. 3.

Discussion

Overview

In the present study, we examined the relationship between LPC/LPOJ sulcal morphology, functional connectivity fingerprints, and cognition. We report five main findings. First, while manually defining sulci in LPC/LPOJ across 144 hemispheres, we uncovered four new small and shallow sulci that are not included in present or classic neuroanatomy atlases or neuroimaging software packages. Second, we found that the most common of these structures (the slocs-v; identifiable 98.6% of the time) was morphologically, architecturally, and functionally differentiable from nearby sulci. Third, using a model-based, data-driven approach quantifying the relationship between sulcal morphology and cognition, we found a relationship between the depths of six LPC/LPOJ sulci and performance on a spatial orientation processing task. Fourth, the model identified distinct dorsal and ventral sulcal networks in LPC/LPOJ: ventral sulci had negative weights while dorsal sulci had positive weights (Fig. 3b). These findings are consistent with previous neuroimaging work from Gur et al. (Gur et al., 2000) who demonstrated separate functional activations in dorsal parietal and the more ventrally situated occipital-parietal cortices for the judgment of line orientation task used in the present study. Fifth, the model identified that the slocs-v is cognitively relevant, further indicating the importance of this new neuroanatomical structure. In the sections below, we discuss (i) the slocs-v relative to modern functional and cytoarchitectonic parcellations in the LPC/LPOJ, as well as anatomical connectivity to other parts of the brain, (ii) underlying anatomical mechanisms relating sulcal morphology and behavior more broadly, and (iii) limitations of the present study. Implications for future studies are distributed throughout each section.

The slocs-v relative to modern functional and cytoarchitectonic parcellations in the LPC/LPOJ, as well as anatomical connectivity to other parts of the brain

To lay the foundation for future studies relating the newly-identified slocs-v to different anatomical and functional organizational features of LPC/LPOJ, we situate probabilistic predictions of slocs-v relative to probabilistic cortical areas identified using multiple modalities. For example, when examining the correspondence between the slocs-v and modern multimodal (HCP-MMP (Glasser et al., 2016)) and observer-independent cytoarchitectural (Julich-Brain atlas (Amunts et al., 2020)) areas (Methods), the slocs-v is located within distinct areas. In particular, the slocs-v aligns with the multimodally- and cytoarchitecturally-defined area PGp bilaterally and cytoarchitecturally-defined hIP4 in the right hemisphere (Fig. 4). In classic neuroanatomical terms (Cunningham, 1892), this indicates that the slocs-v is a putative “axial sulcus” for these regions, which future work can assess with analyses in individual participants.

Fig. 4.

Aside from recent multimodal and observer-independent cytoarchitectonic parcellations, an immediate question is: What is the relationship between the slocs-v and other functional regions at this junction between the occipital and parietal lobes, as well as potential anatomical connectivity? For example, there are over a dozen visual field maps in the cortical expanse spanning the TOS, IPS-PO, and the IPS proper (see (i), (ii), and (iii), respectively in Fig. 5a) (Mackey et al., 2017). When projecting probabilistic locations of retinotopic maps from over 50 individuals from Wang and colleagues (Wang et al., 2015) (Methods), the slocs-v is likely located outside of visual field maps extending into this cortical expanse (Fig. 5a). Nevertheless, when also projecting the map of the mean R² metric from the HCP retinotopy dataset from 181 participants shared by Benson and colleagues (Benson et al., 2018) (Methods), the slocs-v is in a cortical expanse that explains a significant amount of variance (left hemisphere: R² = 19.29, R² = 41.73; right hemisphere: R² = 21.17, R² = 44.23; Fig. 5b).

Fig. 5.

In terms of anatomical connectivity, as the slocs-v co-localizes with cytoarchitectonically defined PGp (Fig. 4) and previous studies have examined the anatomical connectivity of the probabilistically defined PGp, we can glean insight regarding the anatomical connectivity of slocs-v from these previous studies (Caspers et al., 2011; Wang et al., 2012). This prior work showed that PGp was anatomically connected to temporo-occipital regions, other regions in the temporal lobe, middle and superior frontal cortex, as well as the inferior frontal cortex and insula (Caspers et al., 2011; Wang et al., 2012). Furthermore, the slocs-v appears to lie at the junction of scene-perception and place-memory activity (a transition that also consistently co-localizes with the HCP-MMP area PGp) as identified by Steel and colleagues(Steel et al., 2021). Of course, the location of the slocs-v relative to multimodal, cytoarchitectonic, and retinotopic areas, as well as the anatomical connectivity of the slocs-v, would need to be examined in individual participants, but the present work makes clear predictions for future studies as fleshed out here. To conclude this section, as the multimodal area PGp (Fig. 4) was recently proposed as a “transitional area” by Glasser and colleagues (Glasser et al., 2016) (Supplementary Table 1), future studies can also further functionally and anatomically test the transitional properties of slocs-v.

Underlying anatomical mechanisms relating sulcal morphology and behavior

In this section, we discuss potential anatomical mechanisms contributing to the relationship between sulcal depth and behavior in two main ways. First, long-range white matter fibers have a gyral bias, while short-range white matter fibers have a sulcal bias in which some fibers project directly from the deepest points of a sulcus (Cottaar et al., 2021; Reveley et al., 2015; Schilling et al., 2018, 2023; Van Essen et al., 2014). As such, recent work hypothesized a close link between sulcal depth and short-range white matter properties (Bodin et al., 2021; Pron et al., 2021; Voorhies et al., 2021; Willbrand et al., 2023b; Yao et al., 2022): deeper sulci would reflect even shorter short-range white matter fibers, which would result in faster communication between local, cortical regions and in turn, contribute to improved cognitive performance. This increased neural efficiency could underlie individual differences in cognitive performance. Ongoing work is testing this hypothesis which can be further explored in future studies incorporating anatomical, functional, and behavioral measures, as well as computational modeling.

Second, our model-based approach identified separate dorsal and ventral sulcal networks in which deeper sulci dorsally and shallower sulci ventrally contributed to the most explained variance on the spatial orientation task. A similar finding was identified by our previous work in the lateral prefrontal cortex (Yao et al., 2022). These previous and present findings may be explained by the classic anatomical compensation theory, which proposes that the size and depth of a sulcus counterbalance those of the neighboring sulci (Armstrong et al., 1995; Connolly, 1950; Zilles et al., 2013). Thus, a larger, deeper sulcus would be surrounded by sulci that are smaller and shallower, rendering the overall degree of cortical folding within a given region approximately equal (Armstrong et al., 1995; Connolly, 1950; Zilles et al., 2013). Future work can incorporate underlying white matter architecture into the compensation theory, as well as a recent modification that proposed to also incorporate local morphological features such as the deepest sulcal point (e.g., sulcal pit or sulcal root (Régis et al., 2005)), which has recently been shown to be related to different functional features of the cerebral cortex (Bodin et al., 2018; Leroy et al., 2015; Natu et al., 2021). Altogether, these and recent findings begin to build a multimodal mechanistic neuroanatomical understanding underlying the complex relationship between sulcal depth and cognition relative to other anatomical features.

Limitations

The main limitation of our study is that presently, the most accurate methodology to define sulci —especially the small, shallow, and variable tertiary sulci—requires researchers to manually trace each structure on the cortical surface reconstructions. This method is arduous and time-consuming, which, on the one hand, limits the sample size in terms of number of participants, while on the other, results in thousands of precisely defined sulci - a push-pull relationship reflecting a conversation in the broader human brain mapping and cognitive neuroscience fields between a balance of large N studies and “precision imaging” studies in individual participants (Allen et al., 2022; Gratton et al., 2022; Naselaris et al., 2021; Rosenberg and Finn, 2022). Though our sample size is comparable to other studies that produced reliable results relating sulcal morphology to brain function and cognition (e.g., (Cachia et al., 2021; Garrison et al., 2015; Lopez-Persem et al., 2019; Miller et al., 2021; Roell et al., 2021; Voorhies et al., 2021; Weiner, 2019; Willbrand et al., 2022a, 2022b; Yao et al., 2022)), ongoing work that uses deep learning algorithms to automatically define sulci should result in much larger sample sizes in future studies (Borne et al., 2020; Lyu et al., 2021). Finally, the time-consuming manual definitions of primary, secondary, and tertiary sulci also limit the cortical expanse explored in each study, thus, restricting the present study to LPC/LPOJ.

Conclusion

In conclusion, we uncovered four previously-undefined sulci in LPC/LPOJ and quantitatively showed that the slocs-v is a stable sulcal landmark that is morphologically, architecturally, and functionally differentiable from surrounding sulci. We further used a data-driven, model-based approach relating sulcal morphology to behavior, which identified different relationships of ventral and dorsal LPC/LPOJ sulcal networks contributing to the perception of spatial orientation. The model identified the slocs-v, further indicating the importance of this new neuroanatomical structure. Altogether, this work provides a scaffolding for future “precision imaging” studies interested in understanding how anatomical and functional features of LPC/LPOJ relate to cognitive performance at the individual level.

Methods

Participants

Data for the young adult human cohort analyzed in the present study were from the Human Connectome Project (HCP) database (https://www.humanconnectome.org/study/hcp-young-adult/overview). Here, we used 72 participants (50% female, 22-36 years old, and 90% right-handed; there was no effect of handedness on our behavioral tasks; Supplementary materials) that were also analyzed in several prior studies (Hathaway et al., 2023; Miller et al., 2021, 2020; Willbrand et al., 2023b, 2023c, 2022a). HCP consortium data were previously acquired using protocols approved by the Washington University Institutional Review Board (Mapping the Human Connectome: Structure, Function, and Heritability; IRB # 201204036). Informed consent was obtained from all participants.

Neuroimaging data acquisition

Anatomical T1-weighted (T1-w) MRI scans (0.8 mm voxel resolution) were obtained in native space from the HCP database. Reconstructions of the cortical surfaces of each participant were generated using FreeSurfer (v6.0.0), a software package used for processing and analyzing human brain MRI images (surfer.nmr.mgh.harvard.edu) (Dale et al., 1999; Fischl et al., 1999). All subsequent sulcal labeling and extraction of anatomical metrics were calculated from these reconstructions generated through the HCP’s version of the FreeSurfer pipeline (Glasser et al., 2013).

Behavioral data

In addition to structural and functional neuroimaging data, the HCP also includes a wide range of behavioral metrics from the NIH toolbox (Barch et al., 2013). To relate LPC/LPOJ sulcal morphology to behavior, we leveraged behavioral data related to spatial orientation (Variable Short Penn Line Orientation Test), relational reasoning (Penn Progressive Matrices Test), and processing speed (Pattern Completion Processing Speed Test; Supplementary Methods for task details). We selected these tasks as previous functional neuroimaging studies have shown the crucial role of LPC/LPOJ in relational reasoning and spatial orientation (Gur et al., 2000; Karnath, 1997; Vendetti and Bunge, 2014; Wendelken, 2014), while our previous work relating sulcal morphology to cognition uses processing speed performance as a control behavioral task (Voorhies et al., 2021; Willbrand et al., 2022b).

Anatomical analyses

Manual labeling of LPC sulci

Sulci were manually defined in 72 participants (144 hemispheres) guided by the most recent atlas by Petrides (Petrides, 2019), as well as recent empirical studies (Drudik et al., 2022; Segal and Petrides, 2012; Zlatkina and Petrides, 2014), which together offer a comprehensive definition of cerebral sulcal patterns, including tertiary sulci. For a historical analysis of sulci in this cortical expanse, please refer to Segal & Petrides (Segal and Petrides, 2012) and Zlatkina & Petrides (Zlatkina and Petrides, 2014). Our cortical expanse of interest was bounded by the following sulci and gyri: (i) the postcentral sulcus (PoCS) served as the anterior boundary, (ii) the superior temporal sulcus (STS) served as the inferior boundary, (iii) the superior parietal lobule (SPL) served as the superior boundary, and (iv) the medial and lateral transverse occipital sulci (mTOS and lTOS) served as the posterior boundary. We also considered the following sulci within this cortical expanse: the three different branches of the caudal superior temporal sulcus (posterior to anterior: cSTS3, 2, 1), the supramarginal sulcus (SmgS), posterior intermediate parietal sulcus (pips), sulcus of Brissaud (sB), anterior intermediate parietal sulcus of Jensen (aipsJ), paroccipital intraparietal sulcus (IPS-PO), intraparietal sulcus (IPS), and the superior parietal sulcus (SPS). Of note, the IPS-PO is the portion of the IPS extending ventrally into the occipital lobe. The IPS-PO was first identified as the paroccipital sulcus by Wilder (1886). There is often an annectant gyrus separating the horizontal portion of the IPS proper from the IPS-PO (Roell et al., 2021; Zlatkina and Petrides, 2014).

Additionally, we identified as many as four previously uncharted and variable tertiary LPC/LPOJ sulci for the first time: the supralateral occipital sulcus (slocs; composed of ventral (slocs-v) and dorsal (slocs-d) components) and the posterior angular sulcus (pAngs; composed of ventral (pAngs-v) and dorsal (pAngs-d) components). In the Supplementary Methods and Supplementary Figs. 1-4, we discuss the slocs and pAngs within the context of modern and historical sources.

For each participant in each hemisphere, the location of each sulcus was confirmed by trained independent raters (E.H.W., Y.T., and T.G.) and finalized by a neuroanatomist (K.S.W.). All LPC sulci were then manually defined in FreeSurfer using tksurfer tools, as in previous work (Hathaway et al., 2023; Miller et al., 2021, 2020; Parker et al., 2023; Voorhies et al., 2021; Willbrand et al., 2023b, 2023c, 2022a, 2022b; Yao et al., 2022), from which morphological and anatomical features were extracted. For four example hemispheres with these 13-17 sulci identified, see Fig. 1a (Supplementary Fig. 5 for all hemispheres). The specific criteria to identify the slocs and pAngs are outlined in Fig. 1b.

To test whether the incidence rates of the slocs and pAngs components were statistically different, we implemented a binomial logistic regression GLM with sulcus (slocs-v, slocs-d, pAngs-v, and pAngs-d) and hemisphere (left and right), as well as their interaction, as predictors for sulcal presence [0 (absent), 1 (present)]. GLMs were carried out with the glm function from the built-in stats R package. ANOVA χ2 tests were applied to each GLM with the Anova function from the car R package, from which results were reported.

Probability maps

Sulcal probability maps were generated to show the vertices with the highest alignment across participants for a given sulcus. To create these maps, the label file for each sulcus was transformed from the individual to the fsaverage surface with the FreeSurfer mri_label2label command (https://surfer.nmr.mgh.harvard.edu/fswiki/mri_label2label). Once each label was transformed into this common template space, we calculated the proportion of participants for which each vertex was labeled as the given sulcus with custom Python code (Miller et al., 2021; Voorhies et al., 2021). For vertices with overlap between sulci, we employed a “winner-take-all” approach such that the sulcus with the highest overlap across participants was assigned to that vertex. Alongside the thresholded maps, we also provide constrained maps [maximum probability maps (MPMs)] at 20% participant overlap to increase interpretability (20% MPMs shown in Supplementary Fig. 6). To aid future studies interested in investigating LPC/LPOJ sulci, we share these maps with the field.

Extracting and comparing the morphological and architectural features from sulcal labels

Morphologically, we compared sulcal depth and surface area across sulci, as these are two of the primary morphological features used to define and characterize sulci (Armstrong et al., 1995; Chi et al., 1977; Leroy et al., 2015; Lopez-Persem et al., 2019; Miller et al., 2021, 2020; Natu et al., 2021; Sanides, 1964; Voorhies et al., 2021; Weiner, 2019; Welker, 1990; Willbrand et al., 2023b, 2022a; Yao et al., 2022). As in our prior work (Voorhies et al., 2021; Yao et al., 2022), mean sulcal depth values (in standard FreeSurfer units) were computed in native space from the .sulc file generated in FreeSurfer (Dale et al., 1999) with custom Python code (Voorhies et al., 2021). Briefly, depth values are calculated based on how far removed a vertex is from what is referred to as a “mid-surface,” which is determined computationally so that the mean of the displacements around this “mid-surface” is zero. Thus, generally, gyri have negative values, while sulci have positive values. Each depth value was also normalized by the deepest point in the given hemisphere. Surface area (mm²) was calculated with the FreeSurfer mris_anatomical_stats function (https://surfer.nmr.mgh.harvard.edu/fswiki/mris_anatomical_stats). The morphological features of all LPC/LPOJ sulci are documented in Supplementary Fig. 7.

Architecturally, we compared cortical thickness and myelination, as in our prior work in other cortical expanses (Miller et al., 2021; Voorhies et al., 2021; Willbrand et al., 2023b, 2022a). Mean gray matter cortical thickness (mm) was extracted using the FreeSurfer mris_anatomical_stats function. To quantify myelin content, we used the T1-w/T2-w maps for each hemisphere, an in vivo myelination proxy (Glasser and Van Essen, 2011). To generate the T1-w/T2-w maps, two T1-w and T2-w structural MR scans from each participant were registered together and averaged as part of the HCP processing pipeline (Glasser et al., 2013). The averaging helps to reduce motion-related effects or blurring. Additionally, and as described by Glasser and colleagues (Glasser et al., 2013), the T1-w/T2-w images were bias-corrected for distortion effects using field maps. We then extracted the average T1-w/T2-w ratio values across each vertex for each sulcus using custom Python code (Miller et al., 2021). The architectural features of all LPC/LPOJ sulci are documented in Supplementary Fig. 7.

To assess whether these four metrics differed between the slocs-v and surrounding sulci (cSTS3 and lTOS), we ran a repeated measure analysis of variance (rm-ANOVA) with the within-participant effects of sulcus (slocs-v, cSTS3, and lTOS), metric (surface area, depth, cortical thickness, and myelination), and hemisphere (left and right). Rm-ANOVAs (including sphericity correction) were implemented with the aov_ez function from the afex R package. Effect sizes for the ANOVAs are reported with the partial eta-squared metric (η2). Post-hoc analyses were computed with the emmeans function from the emmeans R package (p-values corrected with Tukey’s method). We also repeated these analyses for the three cSTS components (Petrides, 2019; Segal and Petrides, 2012) and the two intermediate parietal sulcal components (ips: aipsJ and pips (Petrides, 2019; Zlatkina and Petrides, 2014); detailed in the Supplementary Results and Supplementary Fig. 8) as these components, to our knowledge, have not been quantitatively compared in previous work.

Functional analyses

To determine if the slocs-v is functionally distinct from surrounding sulci, we generated functional connectivity profiles using recently developed analyses (Miller et al., 2021; Willbrand et al., 2023a, 2022a). First, we used resting-state network parcellations for each individual participant from Kong and colleagues (Kong et al., 2019), who generated individual network definitions by applying a hierarchical Bayesian network algorithm to produce maps for each of the 17 networks in individual HCP participants. Importantly, this parcellation was conducted blind to both cortical folding and our sulcal definitions. Next, we resampled the network profiles for each participant onto the fsaverage cortical surface, and then to each native surface using CBIG tools (https://github.com/ThomasYeoLab/CBIG). We then calculated the spatial overlap between a sulcus and each of the 17 individual resting-state networks via the Dice coefficient (Equation 1):

This process of calculating the overlap between each sulcus and the 17-network parcellation generated a “connectivity fingerprint” for each sulcus in each hemisphere of each participant. We then ran an rm-ANOVA with within-participant factors of sulcus (slocs-v, cSTS3, and lTOS), network (17 networks), and hemisphere (left and right) to determine if the network profiles (i.e., the Dice coefficient overlap with each network) of the slocs-v was differentiable from the surrounding sulci (i.e., cSTS3 and lTOS). Here we discuss effects related to networks that at least showed minor overlap with one sulcus (i.e., Dice ≥ .10). As in the prior analysis, we also repeated these analyses for the three cSTS components and the two intermediate parietal sulcal components (Supplementary Results and Supplementary Fig. 8).

Behavioral analyses

Model selection

The analysis relating sulcal morphology to spatial orientation and/or reasoning consisted of using a cross-validated least absolute shrinkage and selection operator (LASSO) regression to select the sulci that explained the most variance in the data and determined how much variance is explained by sulcal depth as a predictor of behavior, as implemented in our previous work (Voorhies et al., 2021; Willbrand et al., 2023b; Yao et al., 2022). The depths of all LPC/LPOJ sulci were included as predictors in the LASSO regression model (Supplementary Methods for details on demographic control variables). As the shrinkage parameter (alpha) increases, it decreases the coefficient of each of the sulci to zero except for those with the strongest association. Therefore, this technique highlights the sulci whose morphology was most closely related to behavior. We used cross-validation to optimize the shrinking parameter for the LASSO regression. Conventionally, we selected the model parameters that minimized the cross-validated mean squared error (MSE_cv) (Heinze et al., 2018). The optimization was performed with the GridSearchCV function sklearn in Python, which allowed us to determine the model parameters minimizing the MSE_cv. To evaluate the performance of any model selected by the LASSO regression, as in prior work (Voorhies et al., 2021; Willbrand et al., 2023b; Yao et al., 2022), we measured the model performance for the relevant behavioral task using nested model comparison. With leave-one-out cross-validation (LooCV), we compared the LASSO-selected model with the predictors to a model with all left hemisphere sulci as predictors.

Assessing morphological and behavioral specificity

To assess whether our findings generalized to other anatomical features, we considered cortical thickness, which is consistently studied in cognitive neuroscience studies relating morphology to cognition (Dickerson et al., 2008; Gogtay et al., 2004; Voorhies et al., 2021; Willbrand et al., 2023b; Yao et al., 2022). To do so, we replaced sulcal depth with cortical thickness as the predictive metric in our LASSO-selected model. As with depth, the model was fit to the data with LooCV. To compare the thickness model to the depth model, we used the Akaike Information Criterion (AIC), which provides an estimate of in-sample prediction error and is suitable for non-nested model comparison. By comparing AIC scores, we are able to assess the relative performance of the two models. If the ΔAIC is > 2, it suggests an interpretable difference between models. If the ΔAIC is > 10, it suggests a strong difference between models, with the lower AIC value indicating the preferred model (Wagenmakers and Farrell, 2004). To also ascertain whether the relationship between LPC/LPOJ sulcal depth and cognition is specific to spatial orientation performance, or transferable to other general measures of cognitive processing, we investigated the generalizability of the sulcal-behavior relationship to another widely used measure of cognitive functioning: processing speed (Kail and Salthouse, 1994). Specifically, we used LooCV to predict processing speed instead of spatial orientation score. As with thickness, we compared the two models with the AIC.

Situating the slocs-v within modern group-level cortical parcellations

To putatively relate the slocs-v to modern multimodal (HCP multimodal parcellation, HCP-MMP (Glasser et al., 2016)) and cytoarchitectural (Julich-Brain atlas (Amunts et al., 2020)) regions of the cerebral cortex located in fsaverage template space, we quantified the Dice coefficient overlap between the slocs-v of each participant (resampled to fsaverage space) and the individual regions of interest comprising the HCP-MMP and Julich-Brain parcellations.

Retinotopic response mapping of LPC/LPOJ sulci

To assess whether any of the LPC/LPOJ sulci related to retinotopic representations, we leveraged population receptive field mapping data (Benson et al., 2018). For each sulcal MPM (as the retinotopic data were only available in this template space), we extracted the mean R² values (i.e., the percentage of variance in each vertex explained by the population receptive field model) for vertices that showed meaningful retinotopic responses across participants (thresholded at R² > 10%) (Mackey et al., 2017).

Competing interests

The authors declare no competing financial interests.

Data availability

The processed data required to perform all statistical analyses and reproduce all Figures, as well as the probability maps, are available on GitHub (https://github.com/cnl-berkeley/stable_projects). Anonymized HCP neuroimaging data are publicly available on ConnectomeDB (db.humanconnectome.org). Raw data will be made available from the corresponding author upon request.

Code availability

The code is available on GitHub (https://github.com/cnl-berkeley/stable_projects) and Open Science Framework (https://osf.io/7fwqk/).

Acknowledgements

This research was supported by NSF CAREER Award 2042251 (PI Weiner). Neuroimaging and behavioral data were provided by the HCP, WU-Minn Consortium (PIs: David Van Essen and Kamil Ugurbil; NIH Grant 1U54-MH-091657) funded by the 16 NIH Institutes and Centers that support the NIH Blueprint for Neuroscience Research, and the McDonnell Center for Systems Neuroscience at Washington University. We thank Jacob Miller, Benjamin Parker, and Willa Voorhies for helping develop the analysis pipelines implemented in this project. We also thank the HCP researchers for participant recruitment and data collection and sharing, as well as the participants who participated in the study.