scholarly journals Sixty years of radiocarbon dioxide measurements at Wellington, New Zealand 1954–2014

Author(s):  
Jocelyn C. Turnbull ◽  
Sara E. Mikaloff Fletcher ◽  
India Ansell ◽  
Gordon Brailsford ◽  
Rowena Moss ◽  
...  

Abstract. We present 60 years of Δ14CO2 measurements from Wellington, New Zealand (41° S, 175° E). The record has been extended and fully revised. New measurements have been used to evaluate the existing record and to replace original measurements where warranted. This is the earliest atmospheric Δ14CO2 record and records the rise of the 14C "bomb spike", the subsequent decline in Δ14CO2 as bomb 14C moved throughout the carbon cycle and increasing fossil fuel CO2 emissions further decreased atmospheric Δ14CO2. The initially large seasonal cycle in the 1960s reduces in amplitude and eventually reverses in phase, resulting in a small seasonal cycle of about 2 ‰ in the 2000s. The seasonal cycle at Wellington is dominated by the seasonality of cross-tropopause transport, and differs slightly from that at Cape Grim, Australia, which is influenced by anthropogenic sources in winter. Δ14CO2 at Cape Grim and Wellington show very similar trends, with significant differences only during periods of known measurement uncertainty. In contrast, Northern Hemisphere clean air sites show a higher and earlier bomb 14C peak, consistent with a 1.4-year interhemispheric exchange time. From the 1970s until the early 2000s, the Northern and Southern Hemisphere Δ14CO2 were quite similar, apparently due to the balance of 14C-free fossil fuel CO2 emissions in the north and 14C-depleted ocean upwelling in the south. The Southern Hemisphere sites show a consistent and marked elevation above the Northern Hemisphere sites since the early 2000s, which is most likely due to reduced upwelling of 14C-depleted and carbon-rich deep waters in the Southern Ocean. This developing Δ14CO2 interhemispheric gradient is consistent with recent studies that indicate a reinvigorated Southern Ocean carbon sink since the mid-2000s, and suggests that upwelling of deep waters plays an important role in this change.

2017 ◽  
Vol 17 (23) ◽  
pp. 14771-14784 ◽  
Author(s):  
Jocelyn C. Turnbull ◽  
Sara E. Mikaloff Fletcher ◽  
India Ansell ◽  
Gordon W. Brailsford ◽  
Rowena C. Moss ◽  
...  

Abstract. We present 60 years of Δ14CO2 measurements from Wellington, New Zealand (41° S, 175° E). The record has been extended and fully revised. New measurements have been used to evaluate the existing record and to replace original measurements where warranted. This is the earliest direct atmospheric Δ14CO2 record and records the rise of the 14C bomb spike and the subsequent decline in Δ14CO2 as bomb 14C moved throughout the carbon cycle and increasing fossil fuel CO2 emissions further decreased atmospheric Δ14CO2. The initially large seasonal cycle in the 1960s reduces in amplitude and eventually reverses in phase, resulting in a small seasonal cycle of about 2 ‰ in the 2000s. The seasonal cycle at Wellington is dominated by the seasonality of cross-tropopause transport and differs slightly from that at Cape Grim, Australia, which is influenced by anthropogenic sources in winter. Δ14CO2 at Cape Grim and Wellington show very similar trends, with significant differences only during periods of known measurement uncertainty. In contrast, similar clean-air sites in the Northern Hemisphere show a higher and earlier bomb 14C peak, consistent with a 1.4-year interhemispheric exchange time. From the 1970s until the early 2000s, the Northern and Southern Hemisphere Δ14CO2 were quite similar, apparently due to the balance of 14C-free fossil fuel CO2 emissions in the north and 14C-depleted ocean upwelling in the south. The Southern Hemisphere sites have shown a consistent and marked elevation above the Northern Hemisphere sites since the early 2000s, which is most likely due to reduced upwelling of 14C-depleted and carbon-rich deep waters in the Southern Ocean, although an underestimate of fossil fuel CO2 emissions or changes in biospheric exchange are also possible explanations. This developing Δ14CO2 interhemispheric gradient is consistent with recent studies that indicate a reinvigorated Southern Ocean carbon sink since the mid-2000s and suggests that the upwelling of deep waters plays an important role in this change.


2007 ◽  
Vol 4 (3) ◽  
pp. 178 ◽  
Author(s):  
Ian E. Galbally ◽  
Sarah J. Lawson ◽  
Ian A. Weeks ◽  
Simon T. Bentley ◽  
Rob W. Gillett ◽  
...  

Environmental context. Gaseous organic compounds fuel the production of ozone in the background lower atmosphere. There have been no measurements of many of these compounds in the temperate and polar latitudes of the Southern Hemisphere. Here some first results are presented that show in general much lower concentrations than the Northern Hemisphere, due in part to the lower land surfaces and biomass burning in the Southern Hemisphere. Abstract. Measurements were made of volatile organic compounds (VOCs) at Cape Grim using proton transfer reaction mass spectrometry (PTR-MS) during the Precursors to Particles (P2P) Campaign from 10 February to 1 March 2006. Approximately 14 days of clean air data were obtained along with 4 days of data from when polluted air, first from a smoke plume from a fire on Robbins Island adjacent to the station and then air from Victoria, was present. This paper deals with the results obtained in clean air, the focus of the P2P campaign. The protonated masses and probable VOCs measured in the clean marine air were: methanol, 33; acetonitrile, 42; acetaldehyde, 45; acetone, 59; isoprene, 69; methylvinyl ketone/methacrolein (MVK/MACR), 71; methylethyl ketone, 73; and benzene, 79. The measurements at Cape Grim were in some cases near the detection limit and an analytical challenge. The range of concentrations detected in clean maritime air, the relationship to the limited range of previous measurements in marine air in the Northern Hemisphere tropics, and the physical, chemical and biological processes controlling these compounds in the marine air are discussed. The methanol concentrations observed at Cape Grim are consistent with global modelling, incorporating sources that are mainly of vegetation origin. Isoprene has recently been implicated as a precursor to cloud condensation nuclei over the Southern Ocean. In this snapshot of observations at Cape Grim, Tasmania, isoprene and the isoprene oxidation products MVK and MACR appeared to be absent in air from the Southern Ocean. However, isoprene has a very short atmospheric lifetime and the spatial distribution of its emissions may be very heterogeneous. The concentrations of the other VOCs in marine air at Cape Grim, acetonitrile, acetaldehyde, acetone, methylethyl ketone and benzene, were typically a factor of four lower than that observed over the remote tropical ocean in the Northern Hemisphere. The lower concentrations of carbonyls and their precursor hydrocarbons may indicate a limitation on ozone production potential in the Southern Hemisphere compared with the Northern Hemisphere troposphere. Additional keywords: atmospheric composition, oxygenated volatile organic compounds, proton transfer reaction mass spectrometry, Southern Ocean, volatile organic compounds.


2012 ◽  
Vol 12 (2) ◽  
pp. 815-828 ◽  
Author(s):  
T. Ridder ◽  
C. Gerbig ◽  
J. Notholt ◽  
M. Rex ◽  
O. Schrems ◽  
...  

Abstract. Carbon monoxide (CO) and ozone (O3) have been measured in the Western Pacific (43° N to 35° S) during a ship campaign with Research Vessel Sonne in fall 2009. Observations have been performed using ship-based solar absorption Fourier Transform infrared spectrometry, flask sampling, balloon sounding, and in-situ Fourier Transform infrared analysis. The results obtained are compared to the GEOS-Chem global 3-D chemistry transport model for atmospheric composition. In general, a very good agreement is found between the GEOS-Chem model and all instruments. The CO and O3 distributions show a comparable variability suggesting an impact from the same source regions. Tagged-CO simulations implemented in the GEOS-Chem model make it possible to differentiate between different source processes and source regions. The source regions are verified with HYSPLIT backward trajectory calculations. In the Northern Hemisphere fossil fuel combustion in Asia is the dominant source. European and North American fossil fuel combustion also contribute to Northern Hemispheric CO pollution. In the Southern Hemisphere contributions from biomass burning and fossil fuel combustion are dominant; African biomass burning has a significant impact on Western Pacific CO pollution. Furthermore, in the tropical Western Pacific enhanced upper tropospheric CO within the tropical tropopause layer mainly originates from Indonesian fossil fuel combustion and can be transported into the stratosphere. The source regions of the measured O3 pollution are simulated with a tagged-O3 simulation implemented in the GEOS-Chem model. Similar source regions compared to the tagged-CO simulations are identified by the model. In the Northern Hemisphere contributions from Asia, Europe, and North America are significant. In the Southern Hemisphere emissions from South America, south-east Africa, and Oceania significantly contribute to the measured O3 pollution.


1989 ◽  
Vol 3 (6) ◽  
pp. 721
Author(s):  
DA Duckhouse

Australasian pericomoids, psychodids resembling northern hemisphere species of Pericoma Walker (tribe Pericomini), are mostly members of the tribe Maruinini, here re-defined. Amongst Maruinini, they are like several neotropical genera named by Enderlein (1937), but their actual relationship to Enderlein's genera, and hence their identity, has been a long-standing taxonomic problem. Consideration of extensive new collections and observations made in the southern hemisphere now shows that they consist of the following: Genus Notiocharis Eaton. Tribe Maruinini: genus Didicrum Enderlein, and five new genera, Eremolobulosa, Rotundopteryx, Alloeodidicrurn, Satchellomyia and Ancyroaspis. Of these, the Australian Eremolobulosa is the possible sister group of the European Lobulosa Szabo, and the New Zealand genera Satchellomyia and Ancyroaspis are possible sister groups. Of Enderlein's neotropical genera, five classified by Quate (1963) as synonyms, or in one case a subgenus, of Pericoma (Didicrum, Desmioza, Synmormia, Syntomolaba and Podolepria) are recognised as full genera. A key to Australasian pericomoid genera is provided.


2020 ◽  
Vol 232 ◽  
pp. 02002
Author(s):  
Walter Kutschera ◽  
Gernot Patzelt ◽  
Joerg M. Schaefer ◽  
Christian Schlüchter ◽  
Peter Steier ◽  
...  

A brief review of the movements of Alpine glaciers throughout the Holocene in the Northern Hemisphere (European Alps) and in the Southern Hemisphere (New Zealand Southern Alps) is presented. It is mainly based on glacier studies where 14C dating, dendrochronology and surface exposure dating with cosmogenic isotopes is used to establish the chronology of advances and retreats of glaciers. An attempt is made to draw some general conclusions on the temperature and climate differences between the Northern and Southern Hemisphere.


2012 ◽  
Vol 5 (2) ◽  
pp. 491-520 ◽  
Author(s):  
C. J. O'Brien ◽  
J. A. Peloquin ◽  
M. Vogt ◽  
M. Heinle ◽  
N. Gruber ◽  
...  

Abstract. Coccolithophores are calcifying marine phytoplankton of the class Prymnesiophyceae. They are considered to play an import role in the global carbon cycle through the production and export of organic carbon and calcite. We have compiled observations of global coccolithophore abundance from several existing databases as well as individual contributions of published and unpublished datasets. We estimate carbon biomass using standardised conversion methods and provide estimates of uncertainty associated with these values. The database contains 58 384 individual observations at various taxonomic levels. This corresponds to 12 391 observations of total coccolithophore abundance and biomass. The data span a time period of 1929–2008, with observations from all ocean basins and all seasons, and at depths ranging from the surface to 500 m. Highest biomass values are reported in the North Atlantic, with a maximum of 501.7 μg C l−1. Lower values are reported for the Pacific (maximum of 79.4 μg C l−1) and Indian Ocean (up to 178.3 μg C l−1). Coccolithophores are reported across all latitudes in the Northern Hemisphere, from the Equator to 89° N, although biomass values fall below 3 μg C l−1 north of 70° N. In the Southern Hemisphere, biomass values fall rapidly south of 50° S, with only a single non-zero observation south of 60° S. Biomass values show a clear seasonal cycle in the Northern Hemisphere, reaching a maximum in the summer months (June–July). In the Southern Hemisphere the seasonal cycle is less evident, possibly due to a greater proportion of low-latitude data. The original and gridded datasets can be downloaded from Pangaea (http://doi.pangaea.de/10.1594/PANGAEA.785092).


2009 ◽  
Vol 41 (2) ◽  
pp. 151-178 ◽  
Author(s):  
Gintaras KANTVILAS

AbstractThe genusMycoblastusin cool temperate latitudes of the Southern Hemisphere is reviewed. Eight species are treated in detail:M. bryophilusImshaug ex Kantvilas sp. nov., from Campbell Island and Tasmania;M. campbellianus(Nyl.) Zahlbr.,M. coniophorus(Elix & A.W. Archer) Kantvilas & Elix comb. nov. andM. dissimulans(Nyl.) Zahlbr., all widespread across the austral region;M. disporus(C. Knight) Kantvilas comb. nov., from New Zealand and Tasmania;M. kalioruberKantvilas sp. nov, from Tasmania;M. sanguinarioidesKantvilas sp. nov., from Tasmania and south-eastern Australia; andM. leprarioidesKantvilas & Elix sp. nov., from south-eastern Australia (Victoria). Notes are provided on many other species ofMycoblastus, including those recognised for the Northern Hemisphere, and those originally described from austral regions but now excluded from the genus. Major characters of the genus are discussed, including thallus morphology and chemistry, apothecial pigments and ascus structure. It is suggested that the genus is heterogeneous and that some of its closest affinities may lie with the familyMegalariaceaeand the genusJapewia.


2017 ◽  
Vol 14 (2) ◽  
pp. 106 ◽  
Author(s):  
Robert W. Gillett ◽  
Ian E. Galbally ◽  
Melita D. Keywood ◽  
Jennifer C. Powell ◽  
Gavin Stevenson ◽  
...  

Environmental contextThis study presents the first comprehensive set of ambient atmospheric concentrations of short-chain-chlorinated paraffins in the Southern Hemisphere. The data show a seasonal cycle with a summer maximum and a winter minimum. The seasonal cycle is consistent with temperature dependence of the vapour pressure of the short-chain-chlorinated paraffins resulting in partitioning between the atmosphere and other reservoirs with a secondary modulation by soil moisture. AbstractThe first extensive measurements of short-chain chlorinated paraffins (SCCPs) in the atmosphere of the Southern Hemisphere are presented. The analytical and sampling methodologies used in this Australian study were verified by systematic testing along with two inter-comparisons with Northern Hemisphere laboratories with established SCCP programs. In the ambient atmosphere of Melbourne, Australia, in 2013–14, there was a clear seasonal cycle in SCCP monthly averaged concentrations, these ranging from 28.4ng m–3 in summer to 1.8ng m–3 in winter. Air temperature was the factor most closely related to the seasonal cycle in SCCPs in Melbourne. The average SCCP concentrations observed indoors were less than those observed outdoors. Atmospheric concentrations of SCCPs in Melbourne are more than two orders of magnitude higher than concentrations in the background atmosphere. Surprisingly, the SCCP concentrations in Melbourne are similar to those observed in cities in Japan, South Korea and the United Kingdom, and less than those observed in China. Direct transport of SCCPs in the atmosphere from the Northern Hemisphere emissions to Melbourne is ruled out. Instead elevated concentrations in the Melbourne air-shed are most likely a result of the long-term import of SCCPs as industrial chemicals and within manufactured materials from the Northern Hemisphere so that the use of SCCPs in Melbourne and their consequent release to the environment has produced environmental reservoirs of SCCPs in Melbourne that are comparable with those in some Northern Hemisphere cities. The increase in SCCP concentrations from winter to summer is consistent with the temperature dependence of partitioning of SCCPs between the atmosphere and other reservoirs. Insufficient information exists on SCCP use and its presence in soils and sediments in Australia to indicate whether the atmospheric presence of SCCPs in Melbourne is a legacy issue due to its import and use as a metal cutting agent in past decades or due to ongoing imports of manufactured materials containing SCCPs today.


2021 ◽  
Author(s):  
◽  
Kristen Marie Westfall

<p>The Mytilus edulis species complex, comprised of M. edulis, M. galloprovincialis and M. trossulus, is antitropically distributed in temperate coastal regions of all oceans and main seas of the world. This genus has been heavily studied in the Northern hemisphere but Southern hemisphere populations have received much less attention. This thesis aims to place Southern hemisphere blue mussels into global evolutionary relationships among Mytilus species and investigate aspects of their molecular ecology, including, effects of non-native Northern hemisphere species introductions, biogeography across the Southern hemisphere, regional phylogeographic patterns and population genetics within New Zealand. Southern hemisphere blue mussel phylogenetic reconstruction resulted in the detection of a monophyletic M. galloprovincialis lineage. Two new molecular markers developed with specificity for this lineage and congruence among phylogenetic investigations indicates a panhemispheric distribution of this M. galloprovincialis lineage with implications for naming a new sibling species of the M. edulis complex. This proposed new species, M. meridianus, is distributed in South America, the Kerguelen Islands, New Zealand and Australia at latitudes between ~ 30°S and ~ 55°S. Non-native M. galloprovincialis introduced from the Northern hemisphere have been present in NZ, Australia and Chile for at least ten years and hybridise with native blue mussels. Introgression is observed in New Zealand and Australian but not Chilean hybrid regions. The limited number of introduced mussels in Australia induces hybrid swamping of non-native alleles but an interlineage gender bias towards non-native maternal parents may result in eventual loss of the unique genomic content of native blue mussels in NZ. Southern hemisphere blue mussels form a monophyletic sister clade to a haplogroup shared by Northern hemisphere M. edulis and M. galloprovincialis. Although single gene histories are not congruent with respect to evolutionary relationships within the Northern hemisphere due to introgressive hybridisation after speciation, it is clear that Southern hemisphere blue mussels arose from a species native to the northeast Atlantic Ocean after speciation of the three ‘M. edulis complex’ members. Within the Southern hemisphere monophyletic clade lies three reciprocally monophyletic clades restricted to the geographic regions South America/Kerguelen Islands, New Zealand and Australia. Phylogeographic analysis indicates past gene flow between South American/Kerguelen Islands and New Zealand populations that has ceased at present day and ongoing gene flow between South America and the Kerguelen Islands likely via the West Wind Drift. Within NZ, population subdivision inferred from mtDNA indicates genetic variation is distributed within an east-west phylogeographic split on the North Island. These populations experienced gene flow in the past that has ceased at present day. Microsatellite allele frequencies indicate a different population subdivision within the northwest North Island that has been narrowed down to a 15 km stretch of coastline in a sheltered bay. The abrupt discontinuity within a small geographic area does not conform to classic population subdivision in this broad-cast spawning species, therefore, further investigation into the genomic content of northwest North Island mussels with respect to introgressed non-native genes is warranted. Resolving complex phylogenetic patterns from interspecific introgression is key to understanding the evolutionary history of Southern hemisphere M. galloprovincialis. Further characterisation of hybrid introgression would increase accuracy of (1) inferences of processes contributing to hybridisation dynamics and (2) population subdivision in NZ. Probing the basis for variation of hybridisation dynamics would help to predict the outcomes of Northern hemisphere M. galloprovincialis introductions in other areas of the world.</p>


Radiocarbon ◽  
2013 ◽  
Vol 55 (3) ◽  
pp. 1827-1833
Author(s):  
Hirohisa Sakurai ◽  
Saori Namai ◽  
Emiko Inui ◽  
Fuyuki Tokanai ◽  
Kazuhiro Kato ◽  
...  

Using liquid scintillation counting (LSC) and accelerator mass spectrometry (AMS), radiocarbon concentrations were measured for wine from 8 wineries located in 7 countries in the Northern and Southern hemispheres. The 14C concentrations of ethanol and residual materials in the wine were correlated (correlation coefficient 0.82). The δ14C measurements of wine samples from the mid-latitudes in the Northern Hemisphere were approximately 1l% lower than the extrapolations from Schauinsland data, suggesting a local fossil fuel effect. δ14C measurements from the wine samples from the Southern Hemisphere were higher than those from the Northern Hemisphere. The offsets of the 4 wine δ14C measurements were significant, with values between approximately 8% and 15%. Because the harvest years of the mixed grapes were estimated to be 7–12 yr older than their vintage years, this leads to a caveat when determining the 14C concentrations of the year using the wine vintage.


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