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This book presents an innovative and imaginative reading of contemporary Australian literature in the context of unprecedented ecological crisis. The Australian continent has seen significant, rapid changes to its cultures and land-use from the impact of British colonial rule, yet there is a rich history of Indigenous land-ethics and cosmological thought. By using the age-old idea of ‘cosmos’—the order of the world—to foreground ideas of a good order and chaos, reciprocity and more-than-human agency, this book interrogates the Anthropocene in Australia, focusing on notions of colonisation, farming, mining, bioethics, technology, environmental justice and sovereignty. It offers ‘cosmological readings’ of a diverse range of authors—Indigenous and non-Indigenous—as a challenge to the Anthropocene’s decline-narrative. As a result, it reactivates ‘cosmos’ as an ethical vision and a transculturally important counter-concept to the Anthropocene. Kathrin Bartha-Mitchell argues that the arts can help us envision radical cosmologies of being in and with the planet, and to address the very real social and environmental problems of our era. This book will be of particular interest to scholars and students of Ecocriticism, Environmental Humanities, and postcolonial, transcultural and Indigenous studies, with a primary focus on Australian, New Zealand, Oceanic and Pacific area studies.
Endogenous time of day-dependent modulation of brain activity and visual perception in humans
(2023)
Earth’s rotation and the resulting day-night cycle of solar irradiance causes rhythmic changes in environmental conditions. The circadian system anticipates these predictable challenges and the brain integrates this information with homeostatic cues in order to time behavior accordingly. Humans highly depend on the visual system, which is most drastically affected by planetary rotation, with the most pronounced changes occurring during twilight. Yet, it is still unclear how visual perception and its underlying neural processes are modulated according to the time of day. We thus investigated human brain activity in constant dim light via the fMRI BOLD-signal during resting-state and a close-to-threshold visual detection task over 6 times of the day.
BOLD-variability decreased endogenously at times of twilight in sensory cortices during resting-state and, even more, in the visual cortex during visual perception at these times. Furthermore, the visual cortex BOLD-variability reductions were associated with improved visual detection performance. In contrast, mean BOLD-activations related to visual perception were not significantly modulated by the time of day.
In conclusion, these results imply that the visual cortex BOLD-variability reductions at times of twilight constitute a predictive mechanism facilitating visual perception to compensate for the degraded visual signal quality at these times. Individual chronotype and homeostatic sleep pressure explained part of the BOLD-variability modulation, suggesting a combined circadian and homeostatic regulation. Human activity usually extends into times of twilight, even in preindustrial societies. Therefore, anticipatory optimization of the visual system at twilight may have been crucial for survival and may still be relevant today whenever electric light is not available at these times. Moreover, the findings suggest that endogenous BOLD-variability reductions in sensory cortices constitute a novel general mechanism underlying enhanced close-to-threshold perception, further supporting the biological significance of BOLD-variability.
Using 𝑒+𝑒− collision data corresponding to an integrated luminosity of 7.33 fb−1 recorded by the BESIII detector at center-of-mass energies between 4.128 and 4.226 GeV, we present an analysis of the decay 𝐷+𝑠→𝜋+𝜋−𝑒+𝜈𝑒, where the 𝐷+𝑠 is produced via the process 𝑒+𝑒−→𝐷*±𝑠𝐷∓𝑠. We observe the 𝑓0(980) in the 𝜋+𝜋− system and the branching fraction of the decay 𝐷+𝑠→𝑓0(980)𝑒+𝜈𝑒 with 𝑓0(980)→𝜋+𝜋− measured to be (1.72±0.13stat±0.10syst)×10−3, where the uncertainties are statistical and systematic, respectively. The dynamics of the 𝐷+𝑠→𝑓0(980)𝑒+𝜈𝑒 decay are studied with the simple pole parametrization of the hadronic form factor and the Flatté formula describing the 𝑓0(980) in the differential decay rate, and the product of the form factor 𝑓𝑓0+(0) and the 𝑐→𝑠 Cabibbo-Kobayashi-Maskawa matrix element |𝑉𝑐𝑠| is determined for the first time to be 𝑓𝑓0+(0)|𝑉𝑐𝑠|=0.504±0.017stat±0.035syst. Furthermore, the decay 𝐷+
𝑠→𝑓0(500)𝑒+𝜈𝑒 is searched for the first time but no signal is found. The upper limit on the branching fraction of 𝐷+𝑠→𝑓0(500)𝑒+𝜈𝑒, 𝑓0(500)→𝜋+𝜋− decay is set to be 3.3×10−4 at 90% confidence level.
The processes hc→γP(P=η′, η, π0) are studied with a sample of (27.12±0.14)×108 ψ(3686) events collected by the BESIII detector at the BEPCII collider. The decay hc→γη is observed for the first time with the significance of 9.0σ, and the branching fraction is determined to be (3.77±0.55±0.13±0.26)×10−4, while B(hc→γη′) is measured to be (1.40±0.11±0.04±0.10)×10−3, where the first uncertainties are statistical, the second systematic, and the third from the branching fraction of ψ(3686)→π0hc. The combination of these results allows for a precise determination of Rhc=B(hc→γη)B(hc→γη′), which is calculated to be (27.0±4.4±1.0)%. The results are valuable for gaining a deeper understanding of η−η′ mixing, and its manifestation within quantum chromodynamics. No significant signal is found for the decay hc→γπ0, and an upper limit is placed on its branching fraction of B(hc→γπ0)<5.0×10−5, at the 90% confidence level.
Using a sample of about 10 billion J/ψ events with the BESIII detector, we search for the weak decays of J/ψ→D¯0π0+c.c., J/ψ→D¯0η+c.c., J/ψ→D¯0ρ0+c.c., J/ψ→D−π++c.c., and J/ψ→D−ρ++c.c.. Since no significant signal is observed, we set the upper limits of the branching fractions of these decays to be B(J/ψ→D¯0π0+c.c.)<4.7×10−7, B(J/ψ→D¯0η+c.c.)<6.8×10−7, B(J/ψ→D¯0ρ0+c.c.)<5.2×10−7, B(J/ψ→D−π++c.c.)<7.0×10−8, and B(J/ψ→D−ρ++c.c.)<6.0×10−7 at the 90\% confidence level.
We present the first search for the semileptonic decay D+s→π0e+νe using a data sample of electron-positron collisions recorded with the BESIII detector at center-of-mass energies between 4.178 and 4.226~GeV, corresponding to an integrated luminosity of 6.32~fb−1. This decay is expected to be sensitive to π0--η mixing. No significant signal is observed. We set an upper limit of 6.4×10−5 on the branching fraction at the 90% confidence level.
Based on (2.712±0.014)×109 ψ(3686) events collected by the BESIII collaboration, evidence of the hadronic decay hc→K0SK+π−+c.c. is found with a significance of 4.3σ in the ψ(3686)→π0hc process. The branching fraction of hc→K0SK+π−+c.c. is measured to be (7.3±0.8±1.8)×10−4, where the first and second uncertainties are statistical and systematic, respectively. Combining with the exclusive decay width of ηc→KK¯π, our result indicates inconsistencies with both pQCD and NRQCD predictions.
Evidence for the singly Cabibbo suppressed decay Λ+c→pπ0 is reported for the first time with a statistical significance of 3.7σ based on 6.0 fb−1 of e+e− collision data collected at center-of-mass energies between 4.600 and 4.843 GeV with the BESIII detector at the BEPCII collider. The absolute branching fraction of Λ+c→pπ0 is measured to be (1.56+0.72−0.58±0.20)×10−4. Combining with the branching fraction of Λ+c→nπ+, (6.6±1.3)×10−4, the ratio of the branching fractions of Λ+c→nπ+ and Λ+c→pπ0 is calculated to be 3.2+2.2−1.2. As an important input for the theoretical models describing the decay mechanisms of charmed baryons, our result indicates that the non-factorizable contributions play an essential role and their interference with the factorizable contributions should not be significant. In addition, the absolute branching fraction of Λ+c→pη is measured to be (1.63±0.31stat±0.11syst)×10−3.
