One Health challenges for pig reproduction.

The current state of the world challenges pig reproduction as an important part of One Health, which involves interrelationships between animal, human and environmental health. The One Health concept underlines a comparative aspect in reproductive physiology and disease occurrence, bridging knowledge from one species to another. Seasonal changes in the environment affect pig reproduction and climate change may further strengthen those effects. Endocrine-disrupting chemicals (EDCs), and specifically phthalates and heavy metals, interfere with endocrine function, and thereby sexual behavior, fertilization capacity and steroidogenesis. Reproductive infections and extended semen storage are important indications for antimicrobial use. Innovative solutions are needed to explore alternatives to antimicrobials. Efforts to ensure reproductive efficiency have prolonged farrowing as litter size has doubled over the past three decades, compromising immune transfer and welfare. Physiological, metabolic and programming related events around parturition are key areas for future One Health research in pig reproduction. In conclusion, climate change challenges reproductive management and breeding. More resilient pigs that can tolerate harsh environment but maintain high reproductive performance are needed. EDCs continue to grow as an environmental challenge for reproductive management and alternatives to antibiotics will be required.

Facial expressions of pain modulate observer's long-latency responses in superior temporal sulcus.

The strength of brain responses to others' pain has been shown to depend on the intensity of the observed pain. To investigate the temporal profile of such modulation, we recorded neuromagnetic brain responses of healthy subjects to facial expressions of pain. The subjects observed grayscale photos of the faces of genuine chronic pain patients when the patients were suffering from their ordinary pain (Chronic) and when the patients' pain was transiently intensified (Provoked). The cortical activation sequence during observation of the facial expressions of pain advanced from occipital to temporo-occipital areas, and it differed between Provoked and Chronic pain expressions in the right middle superior temporal sulcus (STS) at 300-500 ms: the responses were about a third stronger for Provoked than Chronic pain faces. Furthermore, the responses to Provoked pain faces were about 40% stronger in the right than the left STS, and they decreased from the first to the second measurement session by one-fourth, whereas no similar decrease in responses was found for Chronic pain faces. Thus, the STS responses to the pain expressions were modulated by the intensity of the observed pain and by stimulus repetition; the location and latency of the responses suggest close similarities between processing of pain and other affective facial expressions.

From local to global: Cortical dynamics of contour integration.

Processing of global contours requires integration of local visual information. To study the involvement of different cortical areas and the temporal characteristics of their activity in such integration, we recorded neuromagnetic responses to arrays of Gabor patches in which a proportion of the patches was oriented either tangentially or radially with respect to a global circular contour; arrays with random patch orientations served as control stimuli. The first responses at 60-80 ms around the calcarine sulcus were similar to all stimuli. Starting from 130 ms, responses to the tangential contours differed significantly from responses to control stimuli, and the difference reached its maximum at 275 ms. The most pronounced differences emerged around the parieto-occipital sulcus, precuneus, cuneus, and superior and middle occipital gyri. This pattern of cortical activity was similar irrespective of whether the local elements were radial or tangential to the circle; however, the differences were smaller for the radial contours and tended to start 20-30 ms later. Correspondingly, discrimination reaction times were shortest for the contours consisting of tangential elements. These results demonstrate two spatially and temporally distinct stages of visual cortical processing, the first one limited to local features and the second one integrating information at a more global level.

Face recognition and cortical responses: effect of stimulus duration.

To clarify the relationship between face perception and cortical activation, we manipulated the face recognition performance of 9 subjects by varying the duration (DUR) of stimuli while cortical neuromagnetic responses were recorded. A face image replaced a continuous pixel-noise mask for 17-200 ms, and the subject reported which of the pre-learned faces had been presented. Two cortical responses were clearly stronger to intact than phase-scrambled faces: the temporo-occipital response peaking at 140-200 ms (M170) and a more widely distributed response peaking at 200-500 ms (M300). For the shortest DURs (17-33 ms), face recognition was at chance level and the cortical responses negligible. For DURs of 50-83 ms, the proportion of recognized faces as well as the strength of cortical responses increased steeply. Recognition performance saturated at DURs of around 100 ms, whereas cortical responses continued to increase until the longest DUR of 200 ms. Amplitudes of both M170 and M300 were thus tightly correlated with recognition performance (r=0.98), but comparison of the increment rates as a function of DUR showed the recognition performance to have an even closer similarity to M170 than to M300. In single-trial analysis the variability of response strengths increased in a direct proportion to response amplitude, demonstrating the averaged responses to be composed of graded rather than of all-or-nothing-type single responses.

Estimation of temporal resolution of object identification in human vision.

The purpose of the study was to estimate the temporal processing capacity of human object identification under different stimulus conditions. Objects, either facial images or characters, were shown in a rapid sequence on a computer display using a rapid serial visual presentation (RSVP) method. One of the images was a target and the other images were distracters. The task of the observer was to identify the target. A staircase algorithm was used to determine the threshold frequency of image presentation in the RSVP sequence. The threshold frequency was determined as a function of image contrast, size, and mean luminance. The results showed that the threshold frequency, around 10 Hz for faces (100 ms per face) and about 25 Hz for characters (40 ms per character), was independent of contrast and size at medium and high contrast values, medium and large sizes, and high luminances, but decreased at very low contrasts or small sizes and medium or low levels of luminance. Computer simulations with a model, in which temporal integration limited perceptual speed, suggest that the experimentally found difference in processing time for faces and characters is not due to the physical differences of these stimulus types, but it seems that face-specific sites in the brain process facial information slower than object-specific areas process character information. Contrast, size, and luminance affect the signal-to-noise ratio and the temporal characteristics of low-level neural signal representation. Thus, the results suggest that at low contrasts, low luminances and small sizes, the processing speed of object identification is limited by low-level factors, while at high contrasts and luminances, and at large sizes, processing speed is limited by high-order processing stages. Processing speed seems to depend on stimulus type so that for faces processing is slower than for characters.

Dissociation of face-selective cortical responses by attention.

We studied attentional modulation of cortical processing of faces and houses with functional MRI and magnetoencephalography (MEG). MEG detected an early, transient face-selective response. Directing attention to houses in "double-exposure" pictures of superimposed faces and houses strongly suppressed the characteristic, face-selective functional MRI response in the fusiform gyrus. By contrast, attention had no effect on the M170, the early, face-selective response detected with MEG. Late (>190 ms) category-related MEG responses elicited by faces and houses, however, were strongly modulated by attention. These results indicate that hemodynamic and electrophysiological measures of face-selective cortical processing complement each other. The hemodynamic signals reflect primarily late responses that can be modulated by feedback connections. By contrast, the early, face-specific M170 that was not modulated by attention likely reflects a rapid, feed-forward phase of face-selective processing.

Face recognition and cortical responses show similar sensitivity to noise spatial frequency.

To find cortical correlates of face recognition, we manipulated the recognizability of face images in a parametric manner by masking them with narrow-band spatial noise. Face recognition performance was best at the lowest and highest noise spatial frequencies (NSFs, 2 and 45 c/image, respectively), and degraded gradually towards central NSFs (11-16 c/image). The strength of the 130-180 ms neuromagnetic response (M170) in the temporo-occipital cortex paralleled the recognition performance, whereas the mid-occipital response at 70-120 ms acted in the opposite manner, being strongest for the central NSFs. To noise stimuli without faces, M170 was small and rather insensitive to NSF, whereas the mid-occipital responses resembled closely the responses to the combined face and noise stimuli. These results suggest that the 100 ms mid-occipital response is sensitive to the central spatial frequencies that are critical for face recognition, whereas the M170 response is sensitive to the visibility of a face and closely related to face recognition.