137 research outputs found
Migratory Behavior and Winter Geography Drive Differential Range Shifts of Eastern Birds in Response to Recent Climate Change
Over the past half century, migratory birds in North America have shown divergent population trends relative to resident species, with the former declining rapidly and the latter increasing. The role that climate change has played in these observed trends is not well understood, despite significant warming over this period. We used 43 y of monitoring data to fit dynamic species distribution models and quantify the rate of latitudinal range shifts in 32 species of birds native to eastern North America. Since the early 1970s, species that remain in North America throughout the year, including both resident and migratory species, appear to have responded to climate change through both colonization of suitable area at the northern leading edge of their breeding distributions and adaption in place at the southern trailing edges. Neotropical migrants, in contrast, have shown the opposite pattern: contraction at their southern trailing edges and no measurable shifts in their northern leading edges. As a result, the latitudinal distributions of temperate-wintering species have increased while the latitudinal distributions of neotropical migrants have decreased. These results raise important questions about the mechanisms that determine range boundaries of neotropical migrants and suggest that these species may be particularly vulnerable to future climate change. Our results highlight the potential importance of climate change during the nonbreeding season in constraining the response of migratory species to temperature changes at both the trailing and leading edges of their breeding distributions. Future research on the interactions between breeding and nonbreeding climate change is urgently needed
Heparanase and autoimmune diabetes
Heparanase (Hpse) is the only known mammalian endo-ÎČ-d-glucuronidase that degrades the glycosaminoglycan heparan sulfate (HS), found attached to the core proteins of heparan sulfate proteoglycans (HSPGs). Hpse plays a homeostatic role in regulating the turnover of cell-associated HS and also degrades extracellular HS in basement membranes (BMs) and the extracellular matrix (ECM), where HSPGs function as a barrier to cell migration. Secreted Hpse is harnessed by leukocytes to facilitate their migration from the blood to sites of inflammation. In the non-obese diabetic (NOD) model of autoimmune Type 1 diabetes (T1D), Hpse is also used by insulitis leukocytes to solubilize the islet BM to enable intra-islet entry of leukocytes and to degrade intracellular HS, an essential component for the survival of insulin-producing islet beta cells. Treatment of pre-diabetic adult NOD mice with the Hpse inhibitor PI-88 significantly reduced the incidence of T1D by ~50% and preserved islet HS. Hpse therefore acts as a novel immune effector mechanism in T1D. Our studies have identified T1D as a Hpse-dependent disease and Hpse inhibitors as novel therapeutics for preventing T1D progression and possibly the development of T1D vascular complications.This work was supported by a National Health and Medical
Research Council of Australia (NHMRC)/Juvenile Diabetes
Research Foundation (JDRF) Special Program Grant in Type 1
Diabetes (#418138), a NHMRC Project Grant (#1043284), and a
research grant from the Roche Organ Transplantation Research
Foundation (ROTRF)/JDRF (#477554991)
Loss of intra-islet heparan sulfate is a highly sensitive marker of type 1 diabetes progression in humans
Type 1 diabetes (T1D) is an autoimmune disease in which insulin-producing beta cells in pancreatic islets are progressively destroyed. Clinical trials of immunotherapies in recently diagnosed T1D patients have only transiently and partially impacted the disease course, suggesting that other approaches
are required. Our previous studies have demonstratedthat heparan sulfate (HS), a
glycosaminoglycan conventionally expressed in extracellular matrix, is present at high levels
inside normal mouse beta cells. Intracellular HS was shownto be critical for beta cell survival and
protection from oxidative damage. T1D development
in Non-Obese Diabetic (NOD) mice correlated with loss of islet HS and was prevented by
inhibiting HS degradation by the endoglycosidase, heparanase. In this study we investigated
the distribution of HS and heparan sulfate proteoglycan (HSPG) core proteins in normal
human islets, a role for HS in human beta cell viability and the clinical relevance of intraislet
HS and HSPG levels, compared to insulin, in human T1D. In normal human islets, HS
(identified by 10E4 mAb) co-localized with insulin but not glucagon and correlated with the
HSPG core proteins for collagen type XVIII (Col18) and syndecan-1 (Sdc1). Insulin-positive
islets of T1D pancreases showed significant loss of HS, Col18 and Sdc1 and heparanase
was strongly expressed by islet-infiltrating leukocytes. Human beta cells cultured with HS
mimetics showed significantly improved survival and protection against hydrogen peroxideinduced death, suggesting that loss of HS could contribute to beta cell death in T1D. We conclude that HS depletion in beta cells, possibly due to heparanase produced by insulitis leukocytes, may function as an important
mechanism in the pathogenesis of human T1D.
Our findings raise the possibility that intervention therapy with dual activity HS replacers/
heparanase inhibitors could help to protect the residual beta cell mass in patients recently
diagnosed with T1D.: This work was supported by a National
Health and Medical Research Council of Australia
(NHMRC; https://www.nhmrc.gov.au/)/Juvenile
Diabetes Research Foundation (JDRF) Special
Program Grant in Type 1 Diabetes (#418138), The
Canberra Hospital Private Practice Fund (http://
www.health.act.gov.au/research-publications/research/ppf-major-grants), JDRF nPOD Research
Grant (#25-2010-716; http://www.jdrf.org), JDRF
Research Grant (#47-2012-746) and NHMRC
Project Grant (#1043284
Superconducting undulator activities at the European X-ray Free-Electron Laser Facility
For more than 5 years, superconducting undulators (SCUs) have been successfully delivering X-rays in storage rings. The European X-Ray Free-Electron Laser Facility (XFEL) plans to demonstrate the operation of SCUs in X-ray free-electron lasers (FELs). For the same geometry, SCUs can reach a higher peak field on the axis with respect to all other available technologies, offering a larger photon energy tunability range. The application of short-period SCUs in a high electron beam energy FEL > 11 GeV will enable lasing at very hard X-rays > 40 keV. The large tunability range of SCUs will allow covering the complete photon energy range of the soft X-ray experiments at the European XFEL without changing electron beam energy, as currently needed with the installed permanent magnet undulators. For a possible continuous-wave (CW) upgrade under discussion at the European XFEL with a lower electron beam energy of approximately 7â8 GeV, SCUs can provide the same photon energy range as available at present with the permanent magnet undulators and electron energies. This paper will describe the potential of SCUs for X-ray FELs. In particular, it will focus on the different activities ongoing at the European XFEL and in collaboration with DESY to allow the implementation of SCUs in the European XFEL in the upcoming years
Measurement of the cosmic ray spectrum above eV using inclined events detected with the Pierre Auger Observatory
A measurement of the cosmic-ray spectrum for energies exceeding
eV is presented, which is based on the analysis of showers
with zenith angles greater than detected with the Pierre Auger
Observatory between 1 January 2004 and 31 December 2013. The measured spectrum
confirms a flux suppression at the highest energies. Above
eV, the "ankle", the flux can be described by a power law with
index followed by
a smooth suppression region. For the energy () at which the
spectral flux has fallen to one-half of its extrapolated value in the absence
of suppression, we find
eV.Comment: Replaced with published version. Added journal reference and DO
Energy Estimation of Cosmic Rays with the Engineering Radio Array of the Pierre Auger Observatory
The Auger Engineering Radio Array (AERA) is part of the Pierre Auger
Observatory and is used to detect the radio emission of cosmic-ray air showers.
These observations are compared to the data of the surface detector stations of
the Observatory, which provide well-calibrated information on the cosmic-ray
energies and arrival directions. The response of the radio stations in the 30
to 80 MHz regime has been thoroughly calibrated to enable the reconstruction of
the incoming electric field. For the latter, the energy deposit per area is
determined from the radio pulses at each observer position and is interpolated
using a two-dimensional function that takes into account signal asymmetries due
to interference between the geomagnetic and charge-excess emission components.
The spatial integral over the signal distribution gives a direct measurement of
the energy transferred from the primary cosmic ray into radio emission in the
AERA frequency range. We measure 15.8 MeV of radiation energy for a 1 EeV air
shower arriving perpendicularly to the geomagnetic field. This radiation energy
-- corrected for geometrical effects -- is used as a cosmic-ray energy
estimator. Performing an absolute energy calibration against the
surface-detector information, we observe that this radio-energy estimator
scales quadratically with the cosmic-ray energy as expected for coherent
emission. We find an energy resolution of the radio reconstruction of 22% for
the data set and 17% for a high-quality subset containing only events with at
least five radio stations with signal.Comment: Replaced with published version. Added journal reference and DO
Measurement of the Radiation Energy in the Radio Signal of Extensive Air Showers as a Universal Estimator of Cosmic-Ray Energy
We measure the energy emitted by extensive air showers in the form of radio
emission in the frequency range from 30 to 80 MHz. Exploiting the accurate
energy scale of the Pierre Auger Observatory, we obtain a radiation energy of
15.8 \pm 0.7 (stat) \pm 6.7 (sys) MeV for cosmic rays with an energy of 1 EeV
arriving perpendicularly to a geomagnetic field of 0.24 G, scaling
quadratically with the cosmic-ray energy. A comparison with predictions from
state-of-the-art first-principle calculations shows agreement with our
measurement. The radiation energy provides direct access to the calorimetric
energy in the electromagnetic cascade of extensive air showers. Comparison with
our result thus allows the direct calibration of any cosmic-ray radio detector
against the well-established energy scale of the Pierre Auger Observatory.Comment: Replaced with published version. Added journal reference and DOI.
Supplemental material in the ancillary file
Nucleosomes and DNA methylation shape meiotic DSB frequency in Arabidopsis thaliana transposons and gene regulatory regions.
Meiotic recombination initiates from DNA double-strand breaks (DSBs) generated by SPO11 topoisomerase-like complexes. Meiotic DSB frequency varies extensively along eukaryotic chromosomes, with hotspots controlled by chromatin and DNA sequence. To map meiotic DSBs throughout a plant genome, we purified and sequenced Arabidopsis thaliana SPO11-1-oligonucleotides. SPO11-1-oligos are elevated in gene promoters, terminators, and introns, which is driven by AT-sequence richness that excludes nucleosomes and allows SPO11-1 access. A positive relationship was observed between SPO11-1-oligos and crossovers genome-wide, although fine-scale correlations were weaker. This may reflect the influence of interhomolog polymorphism on crossover formation, downstream from DSB formation. Although H3K4me3 is enriched in proximity to SPO11-1-oligo hotspots at gene 5' ends, H3K4me3 levels do not correlate with DSBs. Repetitive transposons are thought to be recombination silenced during meiosis, to prevent nonallelic interactions and genome instability. Unexpectedly, we found high SPO11-1-oligo levels in nucleosome-depleted Helitron/Pogo/Tc1/Mariner DNA transposons, whereas retrotransposons were coldspots. High SPO11-1-oligo transposons are enriched within gene regulatory regions and in proximity to immunity genes, suggesting a role as recombination enhancers. As transposon mobility in plant genomes is restricted by DNA methylation, we used the met1 DNA methyltransferase mutant to investigate the role of heterochromatin in SPO11-1-oligo distributions. Epigenetic activation of meiotic DSBs in proximity to centromeres and transposons occurred in met1 mutants, coincident with reduced nucleosome occupancy, gain of transcription, and H3K4me3. Together, our work reveals a complex relationship between chromatin and meiotic DSBs within A. thaliana genes and transposons, with significance for the diversity and evolution of plant genomes
The SOLAS air-sea gas exchange experiment (SAGE) 2004
Author Posting. © The Author(s), 2010. This is the author's version of the work. It is posted here by permission of Elsevier B.V. for personal use, not for redistribution. The definitive version was published in Deep Sea Research Part II: Topical Studies in Oceanography 58 (2011): 753-763, doi:10.1016/j.dsr2.2010.10.015.The SOLAS air-sea gas exchange experiment (SAGE) was a multiple-objective study investigating
gas-transfer processes and the influence of iron fertilisation on biologically driven gas exchange in
high-nitrate low-silicic acid low-chlorophyll (HNLSiLC) Sub-Antarctic waters characteristic of the
expansive Subpolar Zone of the southern oceans. This paper provides a general introduction and
summary of the main experimental findings. The release site was selected from a pre-voyage desktop
study of environmental parameters to be in the south-west Bounty Trough (46.5°S 172.5°E) to the
south-east of New Zealand and the experiment conducted between mid-March and mid-April 2004. In
common with other mesoscale iron addition experiments (FeAXâs), SAGE was designed as a
Lagrangian study quantifying key biological and physical drivers influencing the air-sea gas exchange
processes of CO2, DMS and other biogenic gases associated with an iron-induced phytoplankton
bloom. A dual tracer SF6/3He release enabled quantification of both the lateral evolution of a labelled
volume (patch) of ocean and the air-sea tracer exchange at the 10âs of kmâs scale, in conjunction with
the iron fertilisation. Estimates from the dual-tracer experiment found a quadratic dependency of the
gas exchange coefficient on windspeed that is widely applicable and describes air-sea gas exchange in strong wind regimes. Within the patch, local and micrometeorological gas exchange process studies (100 m scale) and physical variables such as near-surface turbulence, temperature microstructure at the interface, wave properties, and wind speed were quantified to further assist the development of gas exchange models for high-wind environments.
There was a significant increase in the photosynthetic competence (Fv/Fm) of resident phytoplankton
within the first day following iron addition, but in contrast to other FeAXâs, rates of net primary
production and column-integrated chlorophyll a concentrations had only doubled relative to the
unfertilised surrounding waters by the end of the experiment. After 15 days and four iron additions
totalling 1.1 tonne Fe2+, this was a very modest response compared to the other mesoscale iron
enrichment experiments. An investigation of the factors limiting bloom development considered co-
limitation by light and other nutrients, the phytoplankton seed-stock and grazing regulation. Whilst
incident light levels and the initial Si:N ratio were the lowest recorded in all FeAXâs to date, there was
only a small seed-stock of diatoms (less than 1% of biomass) and the main response to iron addition
was by the picophytoplankton. A high rate of dilution of the fertilised patch relative to phytoplankton
growth rate, the greater than expected depth of the surface mixed layer and microzooplankton grazing
were all considered as factors that prevented significant biomass accumulation. In line with the limited
response, the enhanced biological draw-down of pCO2 was small and masked by a general increase in pCO2 due to mixing with higher pCO2 waters. The DMS precursor DMSP was kept in check through grazing activity and in contrast to most FeAXâs dissolved dimethylsulfide (DMS) concentration declined through the experiment. SAGE is an important low-end member in the range of responses to iron addition in FeAXâs. In the context of iron fertilisation as a geoengineering tool for atmospheric CO2 removal, SAGE has clearly demonstrated that a significant proportion of the low iron ocean may not produce a phytoplankton bloom in response to iron addition.SAGE was jointly funded through
the New Zealand Foundation for Research, Science and Technology (FRST) programs
(C01X0204) "Drivers and Mitigation of Global Change" and (C01X0223) "Ocean
Ecosystems: Their Contribution to NZ Marine Productivity." Funding was also provided for
specific collaborations by the US National Science Foundation from grants OCE-0326814
(Ward), OCE-0327779 (Ho), and OCE 0327188 OCE-0326814 (Minnett) and the UK Natural
Environment Research Council NER/B/S/2003/00282 (Archer). The New Zealand
International Science and Technology (ISAT) linkages fund provided additional funding
(Archer and Ziolkowski), and the many collaborator institutions also provided valuable
support
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