2,000 research outputs found
A comparison of the moss floras of Chile and New Zealand
Chile and New Zealand share a common stock of 181 species of mosses in 94 genera and 34 families. This number counts for 23.3% of the Chilean and 34.6% of the New Zealand moss flora. If only species with austral distribution are taken into account, the number is reduced to 113 species in common, which is 14.5% of the Chilean and 21.6% of the New Zealand moss flora. This correlation is interpreted in terms of long distance dispersal resp. the common phytogeographical background of both countries as parts of the palaoaustral floristic region and compared with disjunct moss floras of other continents as well as the presently available molecular data
Short-term and long-term effects of toxicants on larval red abalone, Haliotis rufescens
"A thesis presented to the faculty of Moss Landing Marine Laboratories."Thesis (M.S.) -- California State University, Hayward, 1993.by Patrick T. Conroy."A thesis presented to the faculty of Moss Landing Marine Laboratories.
sj-docx-1-hol-10.1177_09596836221126120 – Supplemental material for Implications of sea level variability on the formation and evolution of subtropical Rainbow Beach patterned fen complexes, Queensland, Australia
Supplemental material, sj-docx-1-hol-10.1177_09596836221126120 for Implications of sea level variability on the formation and evolution of subtropical Rainbow Beach patterned fen complexes, Queensland, Australia by Johanna M Hanson, Kevin J Welsh, Patrick T Moss and Patricia Gadd in The Holocene</p
Aspects of the life history of Tresus nuttalli in Elkhorn Slough
by Patrick C. Clark"A thesis presented to the faculty of Moss Landing Marine Laboratories."Thesis (M.S.) -- California State University , Hayward, 1973."A thesis presented to the faculty of Moss Landing Marine Laboratories.
Checklist of the mosses of sub-Saharan Africa
2939 moss taxa are listed for sub-Saharan Africa and adjacent islands, with distribution by country. Each distribution record is supported by a literature reference. The following new combinations are made: Calyptrochaeta cristata (Hedw.) O’Shea, Groutiella elimbata (Thér) O’Shea, Meiothecium undulatum (Ren. & Card.) O’Shea, Orthodontium ruwenzorensis (Thér. & Nav.) O’Shea, Pohlia lacouturei (Thér.) O’Shea, Sematophyllum corticolum (Aongstr.) O’Shea, Sematophyllum dixonii (Thér.) O’Shea, Sematophyllum nanopyxis (Geh.) O’Shea, Sematophyllum rigescens (Card.) O’Shea, and Thamnobryum malgachum (Card.) O’Shea
Late Quaternary vegetation history of North Stradbroke Island, Queensland, eastern Australia
Currently there is a paucity of records of late Quaternary palaeoenvironmental variability available from the subtropics of Australia. The three continuous palaeoecological records presented here, from North Stradbroke Island, subtropical Queensland, assist in bridging this large spatial gap in the current state of knowledge. The dominance of arboreal taxa in the pollen records throughout the past >40,000 years is in contrast with the majority of records from temperate Australia, and indicates a positive moisture balance for North Stradbroke Island. The charcoal records show considerable inter-site variability indicating the importance of local-scale events on individual records, and highlighting the caution that needs to be applied when interpreting a single site as a regional record. The variability in the burning regimes is interpreted as being influenced by both climatic and human factors. Despite this inter-site variability, broad environmental trends are identifiable, with changes in the three records comparable with the OZ-INTIMATE climate synthesis for the last 35,000 years. © 2013 Elsevier Ltd.Patrick T. Moss, John Tibby, Lynda Petherick, Hamish McGowan, Cameron Bar
New synthesis of 2,2 '-heteroarylpyrroles from heteroarylchlorocarbenes
2,2'-Pyridyl- and 2,2'-thienylpyrroles containing substituents at the 1- and 3-positions of the pyrrole ring have been prepared from the reaction of heteroarylchlorocarbenes with 1-azabuta-1,3-dienes. Laser flash photolysis of heteroarylchlorocarbene in isooctane in the presence of 1-azabuta-1,3-diene yields an azomethine ylide (lambda=550 nm) as an intermediate. The kinetic parameters for the ylide formation and further 1,5-intramolecular cyclization to the pyrrole ring have been determined. (C) 1999 Elsevier Science Ltd. All rights reserved.PT: J; CR: BAIRD MS, 1990, J CHEM RES M, P946 ENGEL N, 1978, ANGEW CHEM INT EDIT, V17, P676 GRAHAM WH, 1965, J AM CHEM SOC, V87, P4396 KATRITZKY AR, 1994, SYNTHESIS-STUTTGART, P93 KOROSTOVA SE, 1989, KHIM GETEROTSIKL+, P901 KOTKAR D, 1988, J CHEM SOC CHEM COMM, P917 KOZAKI M, 1996, J ORG CHEM, V61, P3657 LIU MTH, 1994, INT J CHEM KINET, V26, P1179 LUCCHESINI F, 1992, TETRAHEDRON, V48, P9951 MOSS RA, 1987, J AM CHEM SOC, V109, P4341 MOSS RA, 1992, TETRAHEDRON LETT, V33, P1427 NAITOH S, 1986, J CHEM SOC CHEM COMM, P1348 PATIL AO, 1988, CHEM REV, V88, P183 ROMASHIN YN, 1999, CHEM COMMUN 0307, P447 RONCALI J, 1992, CHEM REV, V92, P711 WALTMAN RJ, 1986, CAN J CHEM, V64, P76 ZELIKIN A, 1999, J ORG CHEM, V64, P3379; NR: 17; TC: 11; J9: TETRAHEDRON LETT; PG: 3; GA: 236PXSource type: Electronic(1
A 60 000-year record of environmental change for the Wet Tropics of north-eastern Australia based on the ODP 820 marine core
Palynomorphs from the ODP Site 820 marine core have provided a detailed record of terrestrial environmental responses to glacial–interglacial forcing over the last 250 000 years in the Australian Wet Tropics. The development of an accurate geochronological framework for this key sequence has proved challenging. Consequently, different dominant forcing mechanism(s) have been proposed to drive environmental change in the low latitudes. A new chronology for the last 60 000 years, based on accelerator mass spectrometry radiocarbon (C) dates of pollen concentrate material and the existing Marine Isotope Stage boundaries (MIS 4 to 1) has been produced. This new chronology provides a robust geochronological framework for interpreting environmental records across the region. In particular, our age model helps to resolve several debates concerning the timing of climatic changes and their impacts on both the marine and the terrestrial systems, as well as possible human arrival and associated impacts on the region's ecosystems. Our findings suggest C dating of terrestrial pollen concentrate in marine sediments is a valuable tool for resolving major chronological uncertainties in potentially diagenetically altered marine CaCO sediments and should play a role in future multi-dating strategies. Copyrigh
Benzylchlorocarbene: origins of Arrhenius curvature in the kinetics of the 1,2-H shift rearrangement
Benzylchlorocarbene (1, BCC) was generated photochemically from benzylchlorodiazirine (2) in isooctane, methylcyclohexane (MCH), and tetrachloroethane (TCE) at temperatures from similar to 30 to -75 degrees C. At -70 degrees C in isooctane, the identified products included Z/E-beta-chlorostyrenes 4 (46.6%), alpha-chlorostyrene 5 (2.4%), 1,1-dichloro-2-phenylethane 6 (1.9%), a BCC-isooctane insertion product 8 (5.5%), carbene dimers 9 (3.8%), and azine 3 (30%). The significant incursion of intermolecular products 3, 8, and 9 implies that laser flash photolytic (LFP) kinetic data for the decay of BCC obtained at low temperature is biased and should not be employed in Arrhenius analyses. Accordingly, previously obtained curved Arrhenius correlations for BCC do not necessarily implicate quantum mechanical tunneling (QMT) in the 1,2-H shift rearrangement of BCC to 4. Similarly in MCH, where BCC affords a solvent insertion product in similar to 44-53% yield, the curved Arrhenius correlation (Figure 1) cannot be readily interpreted. In polar solvents such as TCE, clean H-shift reactions of BCC are obtained even at -71 degrees C; an Arrhenius correlation of LFP kinetic data is linear from 3 to -71 degrees C (Figure 2), affording E-a = 3.2 kcal mol(-1) and log A = 10.0 s(-1). Therefore, QMT does not appear to play a major role in the 1,2-H shift rearrangement of BCC at ambient or near ambient temperature in solution.PT: J; CR: BONNEAU R, 1996, J AM CHEM SOC, V118, P3829 DEAN JA, 1992, LANGES HDB CHEM DIX EJ, 1993, J AM CHEM SOC, V115, P10424 DOX AW, 1941, ORG SYNTH, V1, P5 GRAHAM WH, 1965, J AM CHEM SOC, V87, P4396 ISAACS NS, 1995, PHYSICAL ORGANIC CHE, P304 JACKSON JE, 1988, J AM CHEM SOC, V110, P5595 KAZANIS S, 1991, J PHYS CHEM-US, V95, P4430 KEATING AE, 1997, COMMUNICATION 0804 LAVILLA JA, 1989, J AM CHEM SOC, V111, P6877 LAVILLA JA, 1990, TETRAHEDRON LETT, V31, P5109 LIU MTH, 1984, TETRAHEDRON, V40, P887 LIU MTH, 1985, CHEM COMMUN, P982 LIU MTH, 1985, J ORG CHEM, V50, P3218 LIU MTH, 1990, J AM CHEM SOC, V112, P3915 LIU MTH, 1992, J AM CHEM SOC, V114, P3604 LIU MTH, 1992, J PHOTOCH PHOTOBIO A, V63, P115 LIU MTH, 1994, ACCOUNTS CHEM RES, V27, P287 LIU MTH, 1994, J PHOTOCH PHOTOBIO A, V84, P133 MODARELLI DA, 1992, J AM CHEM SOC, V114, P7034 MODARELLI DA, 1993, J AM CHEM SOC, V115, P470 MOSS RA, 1987, J AM CHEM SOC, V109, P4341 MOSS RA, 1990, J AM CHEM SOC, V112, P1638 MOSS RA, 1994, ADV CARBENE CHEM, V1, P59 MOSS RA, 1996, J AM CHEM SOC, V118, P12588 MOSS RA, 1997, CHEM COMMUN 0321, P617 MOSS RA, 1997, TETRAHEDRON LETT, V38, P7049 STORER JW, 1993, J AM CHEM SOC, V115, P10426 SUGIYAMA MH, 1992, J AM CHEM SOC, V114, P966 TOMIOKA H, 1984, J AM CHEM SOC, V106, P454 WHITE WR, 1992, J ORG CHEM, V57, P2841 WIERLACHER S, 1993, J AM CHEM SOC, V115, P8943 YEN VQ, 1962, ANN CHIM, V7, P785; NR: 33; TC: 8; J9: J ORG CHEM; PG: 7; GA: ZM109Source type: Electronic(1
Geochemistry of Moon Point Patterned Fen MP peat core from Australia
Geochemistry data of a high-resolution peat core from the Past Global Changes - Carbon in Peat on EArth through Time (PAGES_C-PEAT) Project
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