A multi‐proxy record of changing environments from ca. 30 000 to 9000 cal. a BP: Onepoto maar palaeolake,Auckland, New Zealand

We present a high‐resolution record of lacustrine sedimentation spanning ca. 30 000 to 9000 cal. a BP from Onepoto maar, northern North Island, New Zealand. The multi‐proxy record of environmental change is constrained by tephrochronology and accelerator mass spectrometric ¹⁴C ages and provides evidence for episodes of rapid environmental change during the Last Glacial Coldest Period (LGCP) and Last Glacial–Interglacial Transition (LGIT) from northern New Zealand. The multi‐proxy palaeoenvironmental record from Onepoto indicates that the LGCP was cold, dry and windy in the Auckland region, with vegetation dominated by herb and grass in a beech forest mosaic between ca. 28 500 and 18 000 cal. a BP. The LGCP was accompanied by more frequent fires and influx of clastic sediment indicating increased erosion during the LGCP, with a mid‐LGCP interstadial identified between ca. 25 000 and 23 000 cal. a BP. Rapid climate amelioration at ca. 18 000 cal. a BP was accompanied by increased terrestrial biomass exemplified by the expansion of lowland podocarp forest, especially Dacrydium cupressinum. Increasing biomass production is reversed briefly by LGIT perturbations which are apparent in many of the proxies that span ca. 14 000–10 500 cal. a BP, suggesting generally increased wetness and higher in situ aquatic plant productivity with reduced terrestrial organic matter and terrigenous detrital influx. Furthermore, conditions at that time were probably warmer and frosts rare based on the increasing importance of Ascarina. The subsequent early Holocene is characterised by podocarp conifer forest and moist mild conditions. Postglacial sea‐level rise breached the crater rim and deposited 36 m of estuarine mud after ca. 9000 cal. a BP. Copyright © 2011 John Wiley & Sons, Ltd.     

Early Permian climate change in the Falkland Islands

An Early Permian glacial diamictite forms a distinctive unit within the Falkland Islands sedimentary succession and two aspects of its significance have recently been serendipitously enhanced. Fossil discoveries in exotic limestone clasts bear on palaeogeography, whilst a series of mineral‐exploration borehole cores have allowed a detailed study of the sedimentary record of deglaciation that followed deposition of the diamictite. Statistical analysis of reflectance and XRF core‐scanning data has identified likely Milankovitch periodicities and enabled tentative time‐scale modelling. The ‘icehouse to greenhouse’ transition appears to have spanned approximately 1.2 million years, with waning cycles of re‐advance superimposed on overall glacial retreat. The new results play into a long‐debated geological paradox: although the Falkland Islands are now proximal to the South Atlantic coastline of South America, their geology bears an uncanny resemblance to that of the Cape Fold Belt and Karoo Basin in South Africa. This puzzled the geological pioneers, but became readily explicable when first continental drift and then plate tectonics were invoked to reconstruct the break‐up of the Gondwana supercontinent—although the details remain controversial. One of the key stratigraphical correlation levels throughout the major fragments of southern Gondwana—South Africa, South America, Antarctica and Australia—is the glacigenic deposit left behind by the extensive, Late Carboniferous to Early Permian regional glaciation; in the Falkland Islands it is designated the Fitzroy Tillite Formation.     

Defining the Potential of Nanoscale Re‐Os Isotope Systematics Using Atom Probe Microscopy

Atom probe microscopy (APM) is a relatively new in situ tool for measuring isotope fractions from nanoscale volumes (< 0.01 μm³). We calculate the theoretical detectable difference of an isotope ratio measurement result from APM using counting statistics of a hypothetical data set to be ± 4δ or 0.4% (2s). However, challenges associated with APM measurements (e.g., peak ranging, hydride formation and isobaric interferences), result in larger uncertainties if not properly accounted for. We evaluate these factors for Re‐Os isotope ratio measurements by comparing APM and negative thermal ionisation mass spectrometry (N‐TIMS) measurement results of pure Os, pure Re, and two synthetic Re‐Os‐bearing alloys from Schwander et al. (2015, Meteoritics and Planetary Science, 50, 893) [the original metal alloy (HSE) and alloys produced by heating HSE within silicate liquid (SYN)]. From this, we propose a current best practice for APM Re‐Os isotope ratio measurements. Using this refined approach, mean APM and N‐TIMS ¹⁸⁷Os/¹⁸⁹Os measurement results agree within 0.05% and 2s (pure Os), 0.6–2% and 2s (SYN) and 5–10% (HSE). The good agreement of N‐TIMS and APM ¹⁸⁷Os/¹⁸⁹Os measurements confirms that APM can extract robust isotope ratios. Therefore, this approach permits nanoscale isotope measurements of Os‐bearing alloys using the Re‐Os geochronometer that could not be measured by conventional measurement principles.     

Estimating urban above ground biomass with multi-scale LiDAR

Background

Urban trees have long been valued for providing ecosystem services (mitigation of the “heat island” effect, suppression of air pollution, etc.); more recently the potential of urban forests to store significant above ground biomass (AGB) has also be recognised. However, urban areas pose particular challenges when assessing AGB due to plasticity of tree form, high species diversity as well as heterogeneous and complex land cover. Remote sensing, in particular light detection and ranging (LiDAR), provide a unique opportunity to assess urban AGB by directly measuring tree structure. In this study, terrestrial LiDAR measurements were used to derive new allometry for the London Borough of Camden, that incorporates the wide range of tree structures typical of an urban setting. Using a wall-to-wall airborne LiDAR dataset, individual trees were then identified across the Borough with a new individual tree detection (ITD) method. The new allometry was subsequently applied to the identified trees, generating a Borough-wide estimate of AGB.

Results

Camden has an estimated median AGB density of 51.6 Mg ha^–1 where maximum AGB density is found in pockets of woodland; terrestrial LiDAR-derived AGB estimates suggest these areas are comparable to temperate and tropical forest. Multiple linear regression of terrestrial LiDAR-derived maximum height and projected crown area explained 93% of variance in tree volume, highlighting the utility of these metrics to characterise diverse tree structure. Locally derived allometry provided accurate estimates of tree volume whereas a Borough-wide allometry tended to overestimate AGB in woodland areas. The new ITD method successfully identified individual trees; however, AGB was underestimated by ≤?25% when compared to terrestrial LiDAR, owing to the inability of ITD to resolve crown overlap. A Monte Carlo uncertainty analysis identified assigning wood density values as the largest source of uncertainty when estimating AGB.

Conclusion

Over the coming century global populations are predicted to become increasingly urbanised, leading to an unprecedented expansion of urban land cover. Urban areas will become more important as carbon sinks and effective tools to assess carbon densities in these areas are therefore required. Using multi-scale LiDAR presents an opportunity to achieve this, providing a spatially explicit map of urban forest structure and AGB.

     

Inter‐laboratory Characterisation of Apatite Reference Materials for Chlorine Isotope Analysis

Here we report on a set of six apatite reference materials (chlorapatites MGMH#133648, TUBAF#38 and fluorapatites MGMH#128441A, TUBAF#37, 40, 50) which we have characterised for their chlorine isotope ratios; these RMs span a range of Cl mass fractions within the apatite Ca₁₀(PO₄)₆(F,Cl,OH)₂ solid solution series. Numerous apatite specimens, obtained from mineralogical collections, were initially screened for ³⁷Cl/³⁵Cl homogeneity using SIMS followed by δ³⁷Cl characterisation by gas source mass spectrometry using both dual‐inlet and continuous‐flow modes. We also report major and key trace element compositions as determined by EPMA. The repeatability of our SIMS results was better than ± 0.10‰ (1s) for the five samples with > 0.5 % m/m Cl and ± 0.19‰ (1s) for the low Cl abundance material (0.27% m/m). We also observed a small, but significant crystal orientation effect of 0.38‰ between the mean ³⁷Cl/³⁵Cl ratios measured on three oriented apatite fragments. Furthermore, the results of GS‐IRMS analyses show small but systematic offset of δ³⁷Cl_SMOC values between the three laboratories. Nonetheless, all studied samples have comparable chlorine isotope compositions, with mean 10³δ³⁷Cl_SMOC values between +0.09 and +0.42 and in all cases with 1s ≤ ± 0.25.     

LA‐ICP‐MS Pb isotope test of meteorite provenance: A terrestrial origin for Lovina

Lovina, classified as an ungrouped ataxite, is controversial and its identity as a meteorite has been questioned. In this work, we use Pb isotopes on targeted troilite nodules in Lovina as a test of its antiquity and provenance. Although precise ages cannot be obtained, LA‐ICP‐MS offers a rapid, straightforward procedure to establish the source of lead, whether ancient (meteoritic) or modern (terrestrial). For nine pristine, unweathered nodules in Lovina, we find a lead isotopic composition of: ²⁰⁶Pb/²⁰⁸Pb = 0.492 ± 0.003 (2σ, MSWD 0.79; 95%) and ²⁰⁷Pb/²⁰⁶Pb = 0.852 ± 0.003 (2σ, MSWD 1.09; 95%) with no detectable uranium. All lead compositions of the troilite fall in the range expected for modern environmental and mantle lead and are distinctly different from the primordial Canyon Diablo Troilite (CDT) composition of ancient meteoritic troilite. Although the origin of Lovina remains unknown, we conclude that lead in the Lovina troilite is unsupported by U decay and originated from a terrestrial source.