Prehistoric timescales, volcanic hazard assessment, and understanding of volcanogenic climate events rely on accurate dating of prehistoric eruptions. Most late Quaternary eruptions are dated by 14C measurements on material from close to the volcano that may be contaminated by geologic-sourced infinite-age carbon. Here we show that 14C ages for the Taupo (New Zealand) First Millennium eruption are geographically arrayed, with oldest ages closer to the vent. The current eruption wiggle match date of 232 ± 5 years CE is amongst the oldest. We present evidence that the older, vent-proximal 14C ages were biased by magmatic CO2 degassed from groundwater, and that the Taupo eruption occurred decades to two centuries after 232 CE. Our reinterpretation implies that ages for other proximally-dated, unobserved, eruptions may also be too old. Plateauing or declining tree ring cellulose δ13C and Δ14C values near a volcano indicate magmatic influence and may allow forecasting of super-eruptions.
Radiometric dating of pre- and early historic volcanic eruptions based on tephra-chronologic control of terrestrial, ice-, lake-, and ocean-core stratigraphy underpins assessment of volcanic hazards1 and volcanogenic climate change2,3. Contamination of samples by carbon containing non-equilibrium levels of 14C can distort radiocarbon ages4,5. The use of inaccurate radiometric eruption dates, particularly for events that occurred remote from contemporary literate societies, can bias a chronology and affect interpretations of data keyed to that chronology, from archaeology6,7 to volcano-climatic connections2,3. Users rarely, however, question the basis for a chronology. A recent example is the anchoring in 2011 of the SP04 (South Pole) ice core chronology8 on the 1980-vintage, 186 CE date9 for the Taupo (New Zealand) First Millennium eruption (hereafter, the Taupo eruption, or “Taupo”), rather than the 1995-vintage, 232 ± 15 years CE date10. The Taupo eruption has a currently accepted date of 232 ± 5 years CE11 and we challenge this date here.
The most recent vent of the Taupo supervolcano lies in the northeast of the 616 km2 caldera Lake Taupo in the central North Island, New Zealand. The lake and caldera are within the central, 125 km long, rhyolite-dominated segment of the Taupo Volcanic Zone (TVZ)12, a ~2 Myr old, actively rifting centre of silicic magmatism. The TVZ hosts a 4.2 GW geothermal system that is fed from shallow (2–7 km deep) heat sources12. The region receives about 1200 mm annual rainfall, which recharges aquifers developed in variably permeable pyroclastic deposits that are increasingly fractured with age/depth and interspersed with lacustrine or paleosol aquitards13. More than 33% of the region’s water wells are < 20 m deep, demonstrating the proximity of the water table to the ground surface.
The Taupo eruption has been the subject of one of the most intensive10,11,14, and earliest15, uses of radiocarbon for dating prehistoric eruptions. The first wiggle match 14C date10 followed >40 14C ages with stratigraphic relationship to one or other of the component tephras of the eruption series16 (Fig. 1). A second, 25-sample, wiggle match date11 on a different tree from the same forest also burnt and buried within the final ignimbrite17 of the Taupo eruption gave a date (232 ± 5 years CE) indistinguishable from the first. The agreement between the results of the two dates, led to the rejection of previously-measured ages, many of which were geologically younger than the wiggle match dates11.
Here we evaluate the pre-wiggle match 14C ages for the Taupo eruption and reveal a relationship between increasing distance from the vent and decreasing 14C age of samples associated with the eruption. We interpret δ13C values of the wiggle match tree samples as indicating contamination by magmatic CO2 injected into the regional groundwater by accumulating basaltic magma beneath the rhyolitic magma chamber. Similar plateauing was observed in records for other eruptions. We suggest that the plateauing of both Δ14C and δ13C values in tree rings could be useful in forecasting major eruptions.
Radiocarbon ages versus distance from vent
We re-examined the corpus of 14C ages for the Taupo eruption, and found a highly significant relationship between the median calibrated SHCal1318 calendar ages and distance from the assumed vent position17, for sites within 60 km from the vent (Fig. 1a). Furthermore, if the material type is considered, the wood and charcoal data sets that contain sufficient samples for age/distance relationship to be evaluated both display the same pattern of younging with increasing distance from the vent as in the aggregate data set (Supplementary Table 1). The median age for the final rings of the second wiggle match tree was amongst the oldest. The median ages are geographically as well as linearly arrayed (Fig. 1b; Supplementary Fig. 1), precluding laboratory error as a basis for differences from the wiggle match ages11. A combined calibrated date (OxCal 4.3, ‘combination’ option) for the non-wiggle match 14C ages of 254 ± 34 CE (median 241 CE) overlapped both wiggle match ages at 1 sigma; and the accompanying probability distribution had a second peak after 300 CE (Fig. 1c).
The peak probabilities for the combination of ages on material <60 km from the vent were in the 170 s and 210 s CE (Fig. 1c), whereas the bimodal probability distribution of the combined ages on material >60 km from the vent had a small older peak c. 250 CE and a much higher peak at c. 310 CE. Combining dates from successively greater distances (60, 70, 100 km) from the vent did not move the overall distribution but increased the size of the later (younger) peak.
The distribution of median values for 50 random radiocarbon ages based on the wiggle match age of 232 CE, with measurement errors set at 25 years (similar to those of the wiggle match series), did not resemble the data range in Fig. 1a, producing only about half the spread of ages and none in the range of the young ages distant from the vent (Supplementary Fig. 2).
Many of the pre-wiggle match radiocarbon measurements were on wood or charcoal and were measured before the possibility of inbuilt age of wood or charcoal (when the sample was from non-peripheral wood or small twigs) was fully taken into account. A possible explanation for old ages is the coincidence that most of the proximal charcoal and wood ages had significant inbuilt ages and that wood and charcoal ages on samples from >60 km from the vent were on short life wood. Inbuilt age bias cannot apply to a wiggle match age so we offer a more likely and mechanistically supported explanation for this geographic array.
Magmatic CO2 in regional groundwater
The radial geographic pattern centred on the volcano (Fig. 1) suggests that volcanic processes, such as the injection19 of magmatic CO2 containing only ‘infinite age’ or ‘old’ carbon (no residual 14C content) have introduced a geographic age bias. Radiocarbon measurements on dissolved inorganic carbon (DIC) in Lake Taupo water, and on plants and animals20 in the lake food web, yielded ages of c. 4000 years on zero-age materials. The ages and anomalously high carbon stable isotope ratios (δ13C) for the DIC, reveal significant (20–42%, Fig. 2) levels of contamination by magmatic carbon (Fig. 2). In addition, radiocarbon ages20 measured on bone protein of a brown rat (Rattus norvegicus, NZA12025, 2139 ± 55 years BP) and of a small duck (New Zealand scaup, Aythya novaeseelandiae, NZA11209, 2674 ± 65 years BP), both collected in 2000 CE at the Lake Taupo shoreline, show that high levels of magmatic carbon still enter the local food web. New Zealand scaup feed on aquatic plants and invertebrates21,22 and brown rats are omnivores, swim well, and in shoreline habitats, as at Lake Taupo, they obtain food by diving23. Therefore, both the duck and rat were obtaining their carbon from the Lake Taupo aquatic food web, and their δ13C values reflect contributions of geologic CO2 to that food web. Another rat, whose 14C age (NZA12024, −261 ± 60 BP)20, was not offset, was part of the terrestrial food web.
Deep groundwaters in the TVZ contain a magmatic CO2 component of 6 ± 2% to 14 ± 5%24. Surface outflow from Lake Taupo potentially perturbs 14C ages of samples downstream from Lake Taupo20, as it does downstream of Long Valley Caldera in California25, but the magmatic CO2 must contaminate the groundwater throughout the volcanic zone, providing a secondary source of CO2 for vegetation26. Even when diluted by recharge from other catchments, the groundwater source of 14C-depleted CO2 would bias radiocarbon dates in the Waikato valley beyond the Taupo volcanic zone20. The wiggle match tree was at 51.8 km from the vent (Supplementary Information Table 1) near the 60-km limit of contamination posited here, but it was only c. 30 km from Lake Taupo and <20 km from the Waikato River. The groundwater is continuous with both the lake and the river so a contamination offset should be present though not necessarily large.
δ13C as an indicator of magmatic CO2 contamination
Potential non-magmatic drivers of differences between δ13C of leaves and wood, and between pre-industrial and present wood include the Suess Effect, fractionation between foliage and wood, and taxon differences. The Suess Effect has been factored into the values plotted in Fig. 2. Wood δ13C values are typically ≤2 ‰ higher than those of leaves27. Typical δ13C values of tree wood and leaves outside volcanic influences range from −32 to −24 ‰28, increasing as they grow into the canopy and gain access to the tropospheric reservoir CO2 (Fig. 2d). In general, vegetation growing beneath dense canopies, even of grass, exhibit low δ13C values in comparison to those for isolated plants or leaves growing within the canopy29,30,31,32. Subcanopy vegetation includes saplings that will possibly mature into canopy trees over a period of decades to a few centuries, so the δ13C values of these saplings, retained in the inner wood of the mature tree, could be up to 10‰ lower than those of the later rings of the mature tree, even with the leaf-wood fractionation. A plot of tree height or ring number against δ13C should be a 'hockey-stick' curve, as is evident in the plot for the Dacrydium in Fig. 2. The wiggle match tree δ13C values depart from this pattern, both in the lack of a substantial tail of low δ13C values in its inner wood and in its anomalously high δ13C values throughout.
Inter-taxic differences in δ13C for C3 plant foliage such as New Zealand forest trees can reach ~3‰ but are minor in relation to those resulting from their positions within closed canopy forests and conditions of growth: all taxa show the same canopy values of foliage δ13C28. Values in wood can reach −22.5 ‰ in isolated trees away from volcanic centres (Fig. 2), but both wiggle match trees10,11 grew in dense forest in a swampy valley33. This environment provided an ideal situation for uptake of respiratory5 and magmatic CO2 by roots26 and (degassed from the soil) subcanopy leaves before it mixed with tropospheric reservoir CO2. The δ13C values (−22 to −20 ‰) of the second wiggle match tree11 were significantly higher than those of New Zealand forest trees (Fig. 2) and lacked the lower range of values in the earliest decades of growth expected for a subcanopy sapling, supporting the view that the tree incorporated magmatic CO2 degassed from local groundwater and taken up through the roots34,35, as well as from the subcanopy air5,30,31,32,36,37.
Moa bone gelatin δ13C as proxy for magmatic CO2 contamination
The bone protein δ13C values (Fig. 2) of four female moa (Euryapteryx curtus) provide indirect support for the influence of groundwater on the level of degassing of old carbon. Soon after post-eruptive revegetation of the Taupo region, five of these large (c. 50 kg), now extinct, herbivorous birds were entombed in a cavity formed by a phreatic explosion immediately post-eruption38 or eroded later in the ignimbrite c. 1.6 km from the present lake shore and 20 km from the vent (Supplementary Fig. 3). One moa yielded a radiocarbon age (NZA34021, 2026 ± 35 conventional 14C years BP; median calibrated date 5 years CE), two centuries older than 232 CE, which is impossible given that the bird’s deposition post-dated the eruption and had to have post-dated the recovery of the vegetation (Supplementary Figs. 3–5). The next oldest (NZA34021, 1617 ± 35 years BP, median calibrated date 485 CE) could have occupied the new vegetation at that date, but it was still 250 years older than the other two birds dated from the deposit (Supplementary Figs. 4, 5).
The minimum offset of 300 years in NZA34021 would require that the sample included at least 3.5% 14C-free carbon. Successive combinations of the radiocarbon ages maintained the date ranges for the three youngest ages, but constraining the oldest moa age to post-eruption violated the combinatorial and phase algorithms (Supplementary Fig. 4) confirming that the oldest moa age, and probably the next, must have been biased by 14C-free carbon in the bird’s diet. Their bone protein δ13C values, which were consistent with those of the second wiggle match tree and significantly higher than values reported for the same moa species elsewhere in New Zealand (Fig. 2; Supplementary Fig. 5), imply contamination by 14C-free carbon in the environment close to the vent, with continued outgassing from the lake and its environs. The comparative δ13C data set encompasses glacial to interglacial climates, from 30 ka to the species’ extinction in the early 15th century CE39.
Other causes are usually invoked for anomalously old 14C ages, where there is a definite date for the organism’s death. For example, a linear relationship between sample δ13C and offset ages on bones of people killed at Herculaneum in 79 CE was attributed to a diet including marine fish. However, we suggest that these anomalous ages may also reflect the effect of magmatic CO2 in the groundwater on the terrestrial components of the diet40 because two 14C ages on a sheep (Ovis aries) metatarsal from the same site, presumably unaffected by a marine diet, were also several decades too old40. The sheep and humans were consuming vegetation that grew on the flanks of Vesuvius41 or within the Campi Flegrei caldera42 and hence the 14C ages of their bones contain a legacy from the CO2 degassed from the magma bodies.
Plateauing of Δ14C and δ13C in wiggle match series
In addition to the δ13C values of the Taupo second wiggle match samples being anomalously high11 (Fig. 2), the δ13C and Δ14C values plateaued successively within the life of the tree (Figs. 2a, 3a, b). After c.135 years and c. 155 years, respectively, linear relationships with actual tree age broke down: the tree continued to grow but 14C ages of the newly accreted wood were static (Fig. 3). The plateau in δ13C values might be interpreted as recording the tree canopy reaching free air above the canopy, but this is improbable given that the δ13C values were much higher than those for New Zealand forest subcanopy vegetation elsewhere43 (Fig. 2), and that the δ13C plateau was followed immediately (in the tree age) by the plateau in Δ14C. The δ13C plateau probably reflects isotopic fractionation of CO2 as it exsolved from the ‘trigger’ basalt beneath the rhyolite reservoir44, and as it degassed from the groundwater.
Fractionation during degassing is governed by the CO2 concentration in the groundwater44: as more magmatic CO2 entered the groundwater, relatively more isotopically light CO2 was degassed, reducing the δ13C of the gas available for photosynthesis. The wood δ13C recorded the net biospheric (and magmatic) CO2 flux, and the Δ14C the total CO2 flux4. Residuals of both Δ14C and δ13C in relation to local regression fits exhibit quasi-periodic variation, which may be related to fluctuations in outgassing of magmatic CO2 beneath the canopy. The period of 30–50 years excludes the possibility that the fluctuations are seasonal. We suggest that wiggle-matched radiocarbon measurements and associated δ13C values should only be made on trees well outside a posited contamination area, which lived and died in the same time frame as the eruption of interest. This would be a fruitful area of future research and an independent test of our contamination hypothesis.
CO2 respired from soil processes (decomposition and respiration) has been shown to bias 14C ages4,5, with 13–28% biospheric CO2 recorded in the canopy air used in generating stem wood cellulose4. At night, CO2 respired by the non-photosynthesising vegetation accumulates beneath a dense canopy4,37, and as the highest net photosynthesis occurs in the morning4, the respired CO2 and any (both biospheric and magmatic) degassed from the soil contributes disproportionately to the stem wood. The effect is further enhanced by the cellulose of the lower part of the stem being produced from CO2 taken up by leaves in the lower interior of the tree’s canopy, where the air is sheltered from mixing with tropospheric CO24. Whereas the 14C age bias attributable to biospheric CO2 is limited by the residence time of soil organic material, significant quantities of magmatic CO2 degassing into the subcanopy air could add decades to millennia to the measured age of both plants and animals within the food web, as shown by the ‘too-old’ ages of the duck, rat, and two moa on the shores of Lake Taupo, and in vegetation growing within the Furnas caldera (Azores)45.
Degassing of CO2 from magma and carbonate rock has been reported from several regions and at different scales46 and may have affected radiocarbon ages for eruptions. Several wiggle match dates47,48 for a major eruption of Baitoushan-Tianchi volcano on the border of North Korea and China, securely dated by dendrochronology to 946 CE49, are variably offset from the calibration curve depending on their location in the forest and distance from the crater. The best wiggle match age of 946 ± 3 CE, from 24 km distance, has a clear old offset from the calibration curve50.
As in the Taupo tree, the δ13C values for the wiggle match trees used to date this eruption ceased to increase over the 30 years before tree death (Fig. 3c–f), a feature also of the data for the Rabaul (Papua New Guinea) eruption51 (Fig. 3g, h). The plateaux or declines in the δ13C values mimic the Suess Effect apparent in the rimu tree growing on the West Coast of the South Island (Fig. 2d), but occurred well before the Industrial Revolution. The volcanic V-Seuss Effect in these wiggle match trees may reflect the different concentration and composition of Taupo (rhyolite/basalt) source CO2 compared with those of the Baitoushan-Tianchi and Rabaul eruptions (both dominantly dacite or andesite). Baitoushan-Tianchi inhabited a favourable section of the calibration curve, with pronounced age peaks and troughs at the eruption age. This highlighted the old offsets of wiggles from the calibration curve and led to unsubstantiated speculations about a magmatic carbon bias50,52. The Rabaul wiggle consisted of only 5 points, anchored by an ambiguous calibration. One age was questionably an outlier. As with all previous ages53, they were obtained on wood that grew <10 km from the caldera rim, so the geographic contexts of the ages are not sufficiently different to show an age–distance relationship. An offset of ~135 years would account for the outlier. The three case studies suggest that more than 50% (and as much as 66%) of volcanic wiggle match ages display evidence for bias by magmatic carbon.
Two dates for the Taupo eruption unbiased by magmatic CO2, were obtained from stratigraphically controlled samples bracketing the ignimbrite in the Hukanui Pool site54,55, c. 68 km from the vent and separated from the Taupo Volcanic Zone by the northern Kaimanawa mountain range (c. 1200 m) (Fig. 1b). The first, for the boundary between eight ages (NZA7635, NZA7181, NZA7184, NZA10199, NZA8559, NZA8226, NZA6636, NZA7532)54 on material below and within, and two (NZA7183, NZA7611)54 above the ignimbrite was 360 ± 79 CE (Fig. 4), close to the peak probability for wiggle match age re-calculated with a uniform contamination by 5% old carbon applied to 25 ages (Fig. 4). A 5% level of contamination is well within that necessary to shift the 14C ages on recent lake shore plants (<4552 radiocarbon years) and animals (>2000 radiocarbon years) cited above20. The most proximal Baitoushan-Tianchi wiggle match ages imply substantially less (0.5%) contamination, but that tree grew, in contrast to the Taupo trees, on a well-drained mountainside, at the tree line of an open forest47,48.
The probability distribution for the boundary between the Hukanui Pool pre- and post-ignimbrite ages had a broad peak (between 295 and 390 CE), with a long 'later' tail, resulting from the greater number of pre-ignimbrite dates. A date of 448 ± 79 CE (Fig. 4) based on the two 14C ages in closest stratigraphic relationship with the ignimbrite, NZA7532 (1715 ± 66 BP, δ13C = −27.9, on a carbonised leaf within the ignimbrite) and NZA7183 (1570 ± 68 BP, δ13C = −19.3) on the tibiotarsus of a flightless rail (Rallidae: Gallirallus australis) on the surface of the ignimbrite)54 is therefore possible.
However, modelled (Oxcal “Phase”, “Date” query) calibrated age ranges for extra-60 km samples were 249–337 CE (68.2%) and 206–388 CE (95.4%). The wiggle match age of 232 ± 4 CE is only just within the 95.4% calibrated date distribution, and far outside the 68.2% distribution and from the middle of both distributions. Applying the OxCal “Combination” option for the same ages on samples >60 km from the vent yielded a 68.2% calibrated age distribution of 248–339 CE (68.2%) and a shorter 95.4% distribution (245–357 CE), both excluding the present wiggle match date. The 68.2% distribution was composed of two distributions: 248–258 CE (9.7%) and 281–339 CE (58.5%). The mean combined date was 299 ± 31 CE, with a median date of 300 CE. It is possible, therefore that the offset resulting from geologic CO2 contamination may be 50–100 years (as above) up to the c. 200 years implied by the Hukanui ages. An unrecognised offset of 50–100 years in a radiocarbon-determined date for an eruption would invalidate any correlation between that eruption date and ice core records or climatic events.
Our demonstration that the 14C samples used to date the Taupo eruption were contaminated by on-edifice magmatic carbon implies that 14C ages on vent-proximal material for other eruptions may be similarly affected by contamination. Stratigraphic chronologies which use the Taupo and other tephras or sulphate signals in the calibration process will need to be reconsidered. The Tierra Blanca Joven eruption of Ilopango volcano, El Salvador, implicated in global climatic events56, is one such, as well as being important in the local archaeology chronology. Further, archaeological radiocarbon chronologies in volcanically active regions, such as the Mediterranean and Central and South America, may require reanalysis. The magnitude of magmatic carbon contamination will depend on the structure of the volcanic edifice and the local climate and exposure of the dated vegetation. For example, the Santorini wiggle match ages57 may be only marginally biased, because the wiggle match olive tree was exposed to strong winds on a mountainside in a dry environment. Errors of a few decades can be significant in some archaeological contexts, as with the 14th century Kaharoa eruption of Mt Tarawera in the Taupo volcanic zone. As a key event in Pacific prehistory chronology6,7, an error of 50 years would significantly affect interpretation of the date of Polynesian settlement of New Zealand.
Our reanalysis of the radiocarbon ages for the Taupo ignimbrite eruption provides the first demonstration of regional biasing of 14C eruption ages by magmatic carbon58. We suggest that the underlying mechanism is injection of magmatic CO2 into the regional groundwater, which has a significant magmatic component24. The results emphasise problems associated with proximal carbon dating and highlight the importance of distal dating of eruptions59, especially those used for stratigraphic correlation. Our methodology for identifying magma carbon bias could result in the re-dating and reinterpretation of many eruptions, with important implications for correlations with climate change, human and animal migration, and cultural adaptation. Finally, we use evidence from three caldera-forming eruptions to suggest that trends in the long-term seasonally-integrated annual records of the carbon isotopic (Δ14C, δ13C) composition of groundwater CO2 in ring sequences from trees growing as part of dense forest canopies in sheltered valleys can provide evidence of injection of magma and hence inform the probability of future eruptions.
All radiocarbon date data are presented in Supplementary Table 1.
Isotopic measurements on the analysis of the Taupo Bypass moa were performed by Isolytix Ltd, Dunedin, New Zealand (Supplementary Table 2) and tree wood were performed by Iso-Trace Ltd, Dunedin, New Zealand, with results reported in relation to standards as set out in Supplementary Table 3.
Tree sampling—carbon stable isotopes in non-volcanic contexts
Two 10-mm diameter cores c. 250 mm long were taken by increment borer from each of two living matai (Prumnopitys taxifolia) trees growing 20 m apart at ‘Glenore’, inland Hawkes Bay, in the eastern North Island, (176.54° E 39.254° S, altitude 736 m). Core holes were sloped c. 5° upwards to prevent retention of rain water. Both trees were sampled to only a fraction of their radius, with ring counts dating to the middle of the 18th century CE (GM1) and the late 17th century (GM2).
A prism was cut from the centre to the bark of the sectioned butt of a wind-thrown rimu (Dacrydium cupressinum) tree on the south bank of the Fox River, Paparoa National Park, on the West Coast, South Island, New Zealand (171.442° E 42.044° S, altitude 68 m).
After drying at 60 °C, the cores and prism were sanded lightly along one face using progressively finer sand paper (to 1200 grit), and the ring patterns imaged using a flatbed scanner. The resulting images were enlarged to facilitate ring counts. No attempt was made to match ring width sequences between trees, as the objective was not dendrochronology per se. The time periods represented by the rings of each tree are only approximate, because we ignored potential errors such as multiple growth rings per year, years lacking rings, and counting errors associated with closely-spaced rings.
Decadal samples were cut from the cores and prism at varying intervals (c. 50 years for the prism samples), powdered in a ball mill and submitted to commercial laboratories for carbon stable isotope analysis. Results, with standards, are given in Supplementary Tables 2 & 3.
Analysis of wiggle match date series
Conventional wiggle match dating involves matching dates from samples separated by independently attested numbers of years (for trees as recorded by annual tree rings) to variations (wiggles) in calibration curves. If a statistically significant match is obtained, age bias is taken to be excluded57. However, if one or more of the ages is measured on material produced by photosynthetic uptake of CO2 containing old carbon, those ages could be offset to the extent that the series could match another section of the curve entirely, unrelated to the actual life span of the tree.
The problem can be avoided, and potential circularity removed, by noting that wiggle match 14C samples are related, to the degrees of certainty inherent in the ring counts57, to each other by a known number of calendar years. The probability distributions of each calibrated age (in calendar time) are therefore independent measures of the calendar age of any other sample from the same tree. The date of interest for an eruption—that of the death of the tree killed by it—is the date of the last (outer) ring: this can be taken as the peak of the summed probability distributions for all the wiggle match ages, each adjusted in time by the ring count between the sample and that of the outer ring (Supplementary Fig. 6). Any level of contamination by infinite-age carbon can then be factored in by adjusting the Δ14C value of the sample(s) by an appropriate amount before calibration. For the second Taupo wiggle match series of 25 14C ages, the date of peak probability for the published ages was identical (232 CE, Fig. 4) to the conventional wiggle match date11, with an associated probability distribution for the eruption date (Fig. 4).
Data are available on request from the corresponding author.
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Isotopic measurements on trees outside the Taupo volcanic zone were obtained under various contracts to Palaecol Research Ltd from the New Zealand Foundation for Research, Science & Technology. B.K. acknowledges support from the New Zealand Ministry of Business Innovation and Employment Endeavour Fund ECLIPSE (Eruption or Catastrophe: Learning to Implement Preparedness for future Supervolcano Eruptions) project. We thank Deborah and Peter Turner (‘Glenore’) and the New Zealand Department of Conservation for permission to sample trees in Hawkes Bay and Paparoa National Park, respectively. Olivia Hyatt processed the Fox River tree section. Gayle Leaf and Doug Wall, hapu monitors representing Tauhara, Rauhoto Ngati Tahu, and Ngati Whaoa iwi approved the examination and sampling of the Taupo Bypass moa material, and Taupo District Council arranged the funding for the aDNA, radiocarbon, and stable isotopic analyses. We thank Mike Bunce (Curtin University, Perth, Western Australia) and Morten Allentoft (Natural History Museum, University of Copenhagen) for the aDNA analyses of the Taupo Bypass moa. David Hawke (Ara Institute of Canterbury) provided guidance on the interpretation of carbon stable isotope fractionation.