Toward defining the Anthropocene onset using a rapid increase in anthropogenic fingerprints in global geological archives.

One of the remaining issues regarding the Anthropocene is the lack of stratigraphic evidence indicating when the cumulative human pressure from the early Holocene began to fundamentally change the Earth system. Herein, we compile anthropogenic fingerprints from various high-precision-dated proxy records for 137 global sites to determine the age of the unprecedented surge in these records over the last 7700 y. The cumulative number of fingerprints revealed an unprecedented surge in diverse anthropogenic fingerprints starting in 1952 ± 3 CE, corresponding to the onset of the Great Acceleration. Notably, the period from 1953 to 1958 CE saw a nearly simultaneous surge in fingerprints across all regions, including Antarctica, the Arctic, East Asia, Europe, North America, and Oceania. This synchronous upsurge reflects the moment when human impacts led to rapid transformations in various natural processes and cycles, with humans becoming a geological force capable of inscribing abundant and diverse anthropogenic fingerprints in global strata. Following this global fingerprint explosion, profound planetary-scale changes, including deviations from the established natural climatic conditions, begin. This unprecedented surge in anthropogenic signals worldwide suggests that human influences started to match many natural forces controlling the processes and cycles and overwhelm some of the functioning of the Earth system around 1952.

Rapid glaciation and a two-step sea level plunge into the Last Glacial Maximum.

The approximately 10,000-year-long Last Glacial Maximum, before the termination of the last ice age, was the coldest period in Earth's recent climate history1. Relative to the Holocene epoch, atmospheric carbon dioxide was about 100 parts per million lower and tropical sea surface temperatures were about 3 to 5 degrees Celsius lower2,3. The Last Glacial Maximum began when global mean sea level (GMSL) abruptly dropped by about 40 metres around 31,000 years ago4 and was followed by about 10,000 years of rapid deglaciation into the Holocene1. The masses of the melting polar ice sheets and the change in ocean volume, and hence in GMSL, are primary constraints for climate models constructed to describe the transition between the Last Glacial Maximum and the Holocene, and future changes; but the rate, timing and magnitude of this transition remain uncertain. Here we show that sea level at the shelf edge of the Great Barrier Reef dropped by around 20 metres between 21,900 and 20,500 years ago, to -118 metres relative to the modern level. Our findings are based on recovered and radiometrically dated fossil corals and coralline algae assemblages, and represent relative sea level at the Great Barrier Reef, rather than GMSL. Subsequently, relative sea level rose at a rate of about 3.5 millimetres per year for around 4,000 years. The rise is consistent with the warming previously observed at 19,000 years ago1,5, but we now show that it occurred just after the 20-metre drop in relative sea level and the related increase in global ice volumes. The detailed structure of our record is robust because the Great Barrier Reef is remote from former ice sheets and tectonic activity. Relative sea level can be influenced by Earth's response to regional changes in ice and water loadings and may differ greatly from GMSL. Consequently, we used glacio-isostatic models to derive GMSL, and find that the Last Glacial Maximum culminated 20,500 years ago in a GMSL low of about -125 to -130 metres.

Initial measurement of beryllium-9 using high-resolution inductively coupled plasma mass spectrometry allows for more precise applications of the beryllium isotope system within the Earth Sciences.

RATIONALE: Precise and accurate determination of the ratio of the cosmogenic nuclide 10 Be to the stable isotope 9 Be (10 Be/9 Be) is needed across multiple fields of research within the Earth Sciences. Current techniques used to measure the 9 Be content of geological materials generally require a large amount of sample or solution aliquot and present a large range of analytical precisions. METHODS: A range of geological reference materials underwent whole-rock dissolution and "strong" (0.04 M NH2 OH.HCl in 25% acetic acid) and "weak" (0.02 M NH2 OH.HCl in 10% acetic acid) leaching to represent a range of potential applications within the geosciences. After treatment, the 9 Be and major element (Na, Ca, Mg, Fe, Mn, Al and Ti) content of sample solutions were determined by high-resolution inductively coupled plasma mass spectrometry (HR-ICP-MS) using a Thermo® ELEMENT XR instrument. RESULTS: The 9 Be concentration of whole-rock and leaching solutions displayed a wide range of values within each geological reference material, generally following a uniform relationship implying a potential kinetic control on NH2 OH leaching, as suggested by major element profiles. A precision of 0.1 to 1.4% is achieved independent of sample size or leaching strength. CONCLUSIONS: Initial results suggest that the use of HR-ICP-MS improves the precision of 9 Be analysis for a range of geological reference materials. A high precision is maintained despite reducing the sample size or strength of leaching solution. This has implications for the use of the Be isotope system within the Earth Sciences by reducing the propagated uncertainty of 10 Be/9 Be ratios or the mass of sample or 9 Be aliquot used.

Holocene melting of the West Antarctic Ice Sheet driven by tropical Pacific warming.

The primary Antarctic contribution to modern sea-level rise is glacial discharge from the Amundsen Sea sector of the West Antarctic Ice Sheet. The main processes responsible for ice mass loss include: (1) ocean-driven melting of ice shelves by upwelling of warm water onto the continental shelf; and (2) atmospheric-driven surface melting of glaciers along the Antarctic coast. Understanding the relative influence of these processes on glacial stability is imperative to predicting sea-level rise. Employing a beryllium isotope-based reconstruction of ice-shelf history, we demonstrate that glaciers flowing into the Amundsen Sea Embayment underwent melting and retreat between 9 and 6 thousand years ago. Despite warm ocean water influence, this melting event was mainly forced by atmospheric circulation changes over continental West Antarctica, linked via a Rossby wave train to tropical Pacific Ocean warming. This millennial-scale glacial history may be used to validate contemporary ice-sheet models and improve sea-level projections.

Plutonium isotopes in the North Western Pacific sediments coupled with radiocarbon in corals recording precise timing of the Anthropocene.

Plutonium (Pu) has been used as a mid-twentieth century time-marker in various geological archives as a result of atmospheric nuclear tests mainly conducted in 1950s. Advancement of analytical techniques allows us to measure 239Pu and 240Pu more accurately and can thereby reconstruct the Pacific Pu signal that originated from the former Pacific Proving Grounds (PPG) in the Marshall Islands. Here, we propose a novel method that couples annual banded reef building corals and nearshore anoxic marine sediments to provide a marker to precisely determine the start of the nuclear era which is known as a part of the Anthropocene. We demonstrate the efficacy of the methods using sediment obtained from Beppu Bay, Japan, and a coral from Ishigaki Island, Japan. The sedimentary records show a clear Pu increase from 1950, peaking during the 1960s, and then showing a sharp decline during the 1970s. However, a constantly higher isotope ratio between 239Pu and 240Pu suggest an additional contribution other than global fallout via ocean currents. Furthermore, single elevations in 240Pu/239Pu provide supportive evidence of close-in-fallout similar to previous studies. Coral skeletal radiocarbon displays a clear timing with the signatures supporting the reliability of the Beppu Bay sediments as archives and demonstrates the strength of this method to capture potential Anthropocene signatures.

Characteristics of high-energy neutrons estimated using the radioactive spallation products of Au at the 500-MeV neutron irradiation facility of KENS.

We carried out a shielding experiment of high-energy neutrons, generated from a tungsten target bombarded with primary 500-MeV protons at KENS, which penetrated through a concrete shield in the zero-degree direction. We propose a new method to evaluate the spectra of high-energy neutrons ranging from 8 to 500 MeV. Au foils were set in a concrete shield, and the reaction rates for 13 radionuclides produced by the spallation reactions on the Au targets were measured by radiochemical techniques. The experimental results were compared with those obtained by the MARS14 Monte-Carlo code. A good agreement (between them) was found for energies beyond 100 MeV. The profile of the neutron spectrum, ranging from 8 to 500 MeV, does not depend on the thickness of the concrete shield.