Seishin Habitus: Spiritual Capital and Japanese Rowing

Sport occupies an important place in educational curriculum, such as club activities in Japanese schools and universities; is it also imbued with what Bourdieu suggests are guaranteed capital properties? That is, can physical education help to accrue capital and can such capital become cultural and economic capital? Further, is this capital similar to that resulting from academic education? Although Western culture recognizes Cartesian differentiation, mind and body are seen as one in the Japanese understanding of the individual, unified by the concept of spirit (this is different to the concept of soul). Recognizing this concept of the body is crucial in addressing the question of transferring educational (in this case physical) capital into forms of cultural capital. This paper investigates the responses of members of a Japanese University Rowing club when addressing questions dealing with various uses of the body in rowing and perceived opportunities for future employment

Remarks on the identification of the Albian/Cenomanian boundary and taxonomic clarification of the planktonic foraminifera index species globotruncanoides, brotzeni and tehamaensis

The planktonic foraminifera assemblage across the Global Boundary Stratotype Section and Point (GSSP) for the base of the Cenomanian Stage defined at Mont Risou (Haute-Alpes in France) is here restudied to clarify the identification and stratigraphic distribution of Thalmanninella globotruncanoides ( = Rotalipora globotruncanoides Sigal, 1948) and Pseudothalmanninella tehamaensis ( = Rotalipora tehamaensis Marianos & Zingula, 1966) whose appearance levels are primary and secondary criteria for placing the Albian/Cenomanian boundary. Since the ratification of the GSSP in 2002, the identification of the foraminifera index species across the Albian/Cenomanian boundary has been reported to be sometimes difficult either because of their rarity or uncertainty in the taxonomic identifications. We discuss the taxonomic status of Thalmanninella brotzeni Sigal 1948, a species regarded for a long time to be a junior synonym of Th. globotruncanoides, through images of Sigal's type materials deposited at the Musée National d’Histoire Naturelle (Paris), and elucidate the taxonomically important characters that enable unequivocal identification of Th. brotzeni, Th. globotruncanoides and Ps. tehamaensis. Planktonic foraminifera marker species from Mont Risou are compared with well-preserved specimens from Blake Nose Plateau (ODP 171B, North Western Atlantic Ocean) to verify the reliability and stratigraphic distribution of these marker taxa outside the Mediterranean Tethyan area

THE MIDDLE EOCENE IN THE ALPINE RETROFORELAND BASIN (NORTHERN ITALY): SEDIMENTARY RECORD OF A “MESO-ALPINE” ARC-TRENCH SYSTEM IN THE ALPS

The middle Eocene Cibrone Formation of Brianza (central-western Lombardy) represents an important stratigraphic record to understand a key step of the tectonic evolution of the Alpine range poorly recorded elsewhere. Quantitative petrographic analysis of turbidite arenites, well-constrained in age by the biostratigraphy of interlayered marlstones based on calcareous foraminifera and nannoplankton, allowed us to identify a possible vertical compositional trend within the Cibrone Fm. and to document the NP17 nannofossil Zone (Bartonian) in central Lombardy exposures, east of the Ternate Formation outcrop area. Variable arenite compositions are interpreted to reflect contributions from different source areas, i.e., recycled orogen, island arc, and starved continental shelf. In a paleogeographic scenario still open to different interpretations, the proposed reconstruction supports a classical plate tectonics model for arc-trench systems. The stratigraphic gap, recorded everywhere in Lombardy, between the Eocene succession and the base of the Gonfolite Lombarda Group (upper NP24 nannofossil Zone, early Chattian), corresponds to the earliest stage of continental collision, uplift and erosion that climaxed in the Neo-Alpine Phase

A systematic review of TMS and neurophysiological biometrics in patients with schizophrenia

Transcranial magnetic stimulation can be combined with electromyography (TMS-EMG) and electroencephalography (TMS-EEG) to evaluate the excitatory and inhibitory functions of the cerebral cortex in a standardized manner. It has been postulated that schizophrenia is a disorder of functional neural connectivity underpinned by a relative imbalance of excitation and inhibition. The aim of this review was to provide a comprehensive overview of TMS-EMG and TMS-EEG research in schizophrenia, focused on excitation or inhibition, connectivity, motor cortical plasticity and the effect of antipsychotic medications, symptom severity and illness duration on TMS-EMG and TMS-EEG indices. We searched PsycINFO, Embase and Medline, from database inception to April 2020, for studies that included TMS outcomes in patients with schizophrenia. We used the following combination of search terms: transcranial magnetic stimulation OR tms AND interneurons OR glutamic acid OR gamma aminobutyric acid OR neural inhibition OR pyramidal neurons OR excita* OR inhibit* OR GABA* OR glutam* OR E-I balance OR excitation-inhibition balance AND schizoaffective disorder* OR Schizophrenia OR schizophreni*. TMS-EMG and TMS-EEG measurements revealed deficits in excitation or inhibition, functional connectivity and motor cortical plasticity in patients with schizophrenia. Increased duration of the cortical silent period (a TMS-EMG marker of γ-aminobutyric acid B receptor activity) with clozapine was a relatively consistent finding. Most of the studies used patients with chronic schizophrenia and medicated patients, employed cross-sectional group comparisons and had small sample sizes. TMS-EMG and TMS-EEG offer an opportunity to develop a novel and improved understanding of the physiologic processes that underlie schizophrenia and to assess the therapeutic effect of antipsychotic medications. In the future, these techniques may also help predict disease progression and further our understanding of the excitatory/inhibitory balance and its implications for mechanisms that underlie treatment-resistant schizophrenia. [Abstract copyright: © 2021 CMA Joule Inc. or its licensors.

The impact of GABAergic drugs on TMS-induced brain oscillations in human motor cortex

Brain responses to transcranial magnetic stimulation (TMS) as measured with electroencephalography (EEG) have so far been assessed either by TMS-evoked EEG potentials (TEPs), mostly reflecting phase-locked neuronal activity, or time-frequency-representations (TFRs), reflecting oscillatory power arising from a mixture of both evoked (i.e., phase-locked) and induced (i.e., non-phase-locked) responses. Single-pulse TMS of the human primary motor cortex induces a specific pattern of oscillatory changes, characterized by an early (30–200 ms after TMS) synchronization in the α- and β-bands over the stimulated sensorimotor cortex and adjacent lateral frontal cortex, followed by a late (200–400 ms) α- and β-desynchronization over the stimulated and contralateral sensorimotor cortex. As GABAergic inhibition plays an important role in shaping oscillatory brain activity, we sought here to understand if GABAergic inhibition contributes to these TMS-induced oscillations. We tested single oral doses of alprazolam, diazepam, zolpidem (positive modulators of the GABAA receptor), and baclofen (specific GABAB receptor agonist). Diazepam and zolpidem enhanced, and alprazolam tended to enhance while baclofen decreased the early α-synchronization. Alprazolam and baclofen enhanced the early β-synchronization. Baclofen enhanced the late α-desynchronization, and alprazolam, diazepam and baclofen enhanced the late β-desynchronization. The observed GABAergic drug effects on TMS-induced α- and β-band oscillations were not explained by drug-induced changes on corticospinal excitability, muscle response size, or resting-state EEG power. Our results provide first insights into the pharmacological profile of TMS-induced oscillatory responses of motor cortex

A systematic review of TMS and neurophysiological biometrics in patients with schizophrenia

Background: Transcranial magnetic stimulation can be combined with electromyography (TMS-EMG) and electroencephalography (TMS-EEG) to evaluate excitatory and inhibitory functions of the cerebral cortex in a standardised manner. Schizophrenia has been postulated to be a disorder of functional neural connectivity underpinned by relative excitation/inhibition imbalance. The aim of this review is to provide a comprehensive overview of TMS-EMG and -EEG research in schizophrenia focused on excitation/inhibition, connectivity, motor cortical plasticity, and the impact of antipsychotic medications, symptom severity and illness duration on TMS-EMG and -EEG indices.Methods: We searched PsycInfo, Embase and Medline, from inception to April 2020, for studies including TMS outcomes in patients with schizophrenia. The following combination of search terms was used: (transcranial magnetic stimulation OR tms) AND (interneurons OR glutamic acid OR gamma aminobutyric acid OR neural inhibition OR pyramidal neurons OR excita* OR inhibit* OR GABA* OR glutam* OR E-I balance OR excitation-inhibition balance) AND (schizoaffective disorder* OR Schizophrenia OR schizophreni*).Results: TMS-EMG and TMS-EEG measurements revealed deficits in excitation/inhibition, functional connectivity and motor cortical plasticity in schizophrenia. Additionally, increased duration of cortical silent period, a TMS-EMG marker of GABAB receptor activity, by clozapine was a relatively consistent finding.Limitations: Most of the studies used chronic and medicated patients, employed cross-sectional group comparisons and had a small patient sample size. Conclusion: TMS-EMG and TMS-EEG offers an opportunity to develop a novel and improved understanding of the physiological processes underlying schizophrenia and assess the therapeutic effect of antipsychotic medications. In the future, the techniques may also help predict disease progression and further our understanding of the excitatory-inhibitory balance and its implications for mechanisms underlying treatment resistant schizophrenia

The Effect of Lamotrigine and Levetiracetam on TMS-Evoked EEG Responses Depends on Stimulation Intensity

The combination of transcranial magnetic stimulation and electroencephalography (TMS-EEG) has uncovered underlying mechanisms of two anti-epileptic medications: levetiracetam and lamotrigine. Despite their different mechanism of action, both drugs modulated TMS-evoked EEG potentials (TEPs) in a similar way. Since both medications increase resting motor threshold (RMT), the current aim was to examine the similarities and differences in post-drug TEPs, depending on whether stimulation intensity was adjusted to take account of post-drug RMT increase. The experiment followed a placebo controlled, double blind, crossover design, involving a single dose of either lamotrigine or levetiracetam. When a drug-induced increase of RMT occurred, post-drug measurements involved two blocks of stimulations, using unadjusted and adjusted stimulation intensity. A cluster based permutation analysis of differences in TEP amplitude between adjusted and unadjusted stimulation intensity showed that lamotrigine induced a stronger modulation of the N45 TEP component compared to levetiracetam. Results highlight the impact of adjusting stimulation intensity

TMS- EEG Signatures of GABAergic Neurotransmission in the Human Cortex

Combining transcranial magnetic stimulation (TMS) and electroencephalography (EEG) constitutes a powerful tool to directly assess human cortical excitability and connectivity. TMS of the primary motor cortex elicits a sequence of TMS-evoked EEG potentials (TEPs). It is thought that inhibitory neurotransmission through GABA-A receptors (GABAAR) modulates early TEPs (<50 ms after TMS), whereas GABA-B receptors (GABABR) play a role for later TEPs (at ∼100 ms after TMS). However, the physiological underpinnings of TEPs have not been clearly elucidated yet. Here, we studied the role of GABAA/B-ergic neurotransmission for TEPs in healthy subjects using a pharmaco-TMS-EEG approach. In Experiment 1, we tested the effects of a single oral dose of alprazolam (a classical benzodiazepine acting as allosteric-positive modulator at α1, α2, α3, and α5 subunit-containing GABAARs) and zolpidem (a positive modulator mainly at the α1 GABAAR) in a double-blind, placebo-controlled, crossover study. In Experiment 2, we tested the influence of baclofen (a GABABR agonist) and diazepam (a classical benzodiazepine) versus placebo on TEPs. Alprazolam and diazepam increased the amplitude of the negative potential at 45 ms after stimulation (N45) and decreased the negative component at 100 ms (N100), whereas zolpidem increased the N45 only. In contrast, baclofen specifically increased the N100 amplitude. These results provide strong evidence that the N45 represents activity of α1-subunit-containing GABAARs, whereas the N100 represents activity of GABABRs. Findings open a novel window of opportunity to study alteration of GABAA-/GABAB-related inhibition in disorders, such as epilepsy or schizophrenia

Recent advances in the study of Eocene planktonic foraminifera

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The spectral features of EEG responses to transcranial magnetic stimulation of the primary motor cortex depend on the amplitude of the motor evoked potentials

Transcranial magnetic stimulation (TMS) of the primary motor cortex (M1) can excite both cortico-cortical and cortico-spinal axons resulting in TMS-evoked potentials (TEPs) and motor-evoked potentials (MEPs), respectively. Despite this remarkable difference with other cortical areas, the influence of motor output and its amplitude on TEPs is largely unknown. Here we studied TEPs resulting from M1 stimulation and assessed whether their waveform and spectral features depend on the MEP amplitude. To this aim, we performed two separate experiments. In experiment 1, single-pulse TMS was applied at the same supra-threshold intensity on primary motor, prefrontal, premotor and parietal cortices and the corresponding TEPs were compared by means of local mean field power and time-frequency spectral analysis. In experiment 2 we stimulated M1 at resting motor threshold in order to elicit MEPs characterized by a wide range of amplitudes. TEPs computed from high-MEP and low-MEP trials were then compared using the same methods applied in experiment 1. In line with previous studies, TMS of M1 produced larger TEPs compared to other cortical stimulations. Notably, we found that only TEPs produced by M1 stimulation were accompanied by a late event-related desynchronization (ERD-peaking at ~300 ms after TMS), whose magnitude was strongly dependent on the amplitude of MEPs. Overall, these results suggest that M1 produces peculiar responses to TMS possibly reflecting specific anatomo-functional properties, such as the re-entry of proprioceptive feedback associated with target muscle activation