@article {109, title = {Two new species of forget-me-nots (Myosotis, Boraginaceae) from New Zealand }, journal = {PhytoKeys}, year = {2012}, month = {2012}, pages = {53 - 64}, publisher = {Pensoft Publishers}, abstract = {Two new species of forget-me-nots, Myosotis chaffeyorum C.A.Lehnebach sp. nov. and Myosotis mooreana C.A.Lehnebach sp. nov. are described and illustrated. These species are endemic to New Zealand and restricted to the mountains of north-west Nelson (South Island). Both species are uncommon and Myosotis mooreana is known from the type locality only. Their conservation status is rated as {\textquotedblleft}Nationally Critical{\textquotedblright}. A table listing differences between these two new species and other similar species and an identification key are provided.}, isbn = {1314-20111314-2003}, url = {http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3492931/}, author = {Lehnebach, Carlos A} } @article {107, title = {Lectotypification of three species of forget-me-nots (Myosotis: Boraginaceae) from Australasia}, journal = {Tuhinga}, volume = {23}, year = {2012}, pages = {17-28}, abstract = {

Lectotypes for the names of one Australasian and two New Zealand native
forget-me-nots are selected: Myosotis australis R. Br., M. forsteri Lehm. and M. goyenii Petrie,
respectively. The collection of the type material of M. forsteri by JR and G. Forster at Dusky
Bay (South Island, New Zealand), and not in Australia, is further supported. Images of all
three lectotypes are included.

}, keywords = {D. Petrie, G. Forster, JGC Lehmann, JR Forster, lectotypes, Myosotis, New Zealand flora, R. Brown}, url = {http://www.tepapa.govt.nz/SiteCollectionDocuments/TePapaPress/Tuhinga23fulltext.pdf$\#$page=21}, author = {Lehnebach, Carlos A} } @article {106, title = {Morphological and amplified fragment length polymorphism (AFLP) data show that New Zealand endemic Myosotis petiolata (Boraginaceae) comprises three rare and threatened species}, journal = {Australian Systematic Botany}, volume = {26}, year = {2013}, month = {2013}, pages = {210 - 232}, abstract = {

Species delimitation is of critical importance in systematics and biological and conservation research. The general-lineage species concept, which defines species as separately evolving metapopulation lineages, considers multiple lines of evidence to identify lineages and delimit species boundaries. Here, we apply the general-lineage concept to the New Zealand endemic Myosotis petiolata Hook.f. (Boraginaceae) species complex, to test its usefulness in the New Zealand Myosotis L. species radiation. We aimed to determine whether the complex contains separately evolving lineages to assess the criteria of monophyly, distinct genotypic clusters and fixed morphological differences by using amplified fragment length polymorphism (AFLP) and morphological data. The use of multiple criteria to identify separately evolving lineages within the M. petiolata complex was effective, but the different criteria were satisfied to varying degrees. Species rank is recommended for each of the currently recognised varieties as Myosotis pottsiana (L.B.Moore) Meudt, Prebble, R.J.Stanley \& Thorsen (comb. \& stat. nov.), M. pansa (L.B.Moore) Meudt, Prebble, R.J.Stanley \& Thorsen (comb. \& stat. nov.) and M. petiolata Hook.f. (North Island individuals only). A new allopatric subspecies, M. pansa subsp. praeceps Meudt, Prebble, R.J.Stanley \& Thorsen (subsp. nov.), is also described. The distinguishing morphological characters and conservation status of each species are discussed. In addition, the low genetic diversity revealed in our population genetic analyses, coupled with few, fluctuating, disjunct populations, underscores the conservation priority of these three rare endemic New Zealand species.

}, doi = {http://dx.doi.org/10.1071/SB13023}, url = {http://www.publish.csiro.au/?paper=SB13023}, author = {Meudt, Heidi M. and Prebble, Jessica M. and Stanley, Rebecca J. and Thorsen, Michael J.} } @article {105, title = {Native New Zealand forget-me-nots (Myosotis, Boraginaceae) comprise a Pleistocene species radiation with very low genetic divergence}, journal = {Plant Systematics and Evolution}, volume = {301}, year = {2015}, month = {2015/05/01}, pages = {1455-1471}, publisher = {Springer Vienna}, abstract = {

Reconstruction of molecular phylogenies is an important step towards understanding the evolutionary history of island plant radiations. The New Zealand forget-me-nots (Myosotis, Boraginaceae) comprise a lineage of over 40 closely related but morphologically and ecologically diverse species whose evolutionary history and taxonomy are unclear. Myosotis is a high priority for systematic research in New Zealand because a high proportion of these species are threatened, and many have restricted geographic ranges and occupy very specific habitats. Here, we investigated the relationships and age of Southern Hemisphere forget-me-nots by performing phylogenetic, molecular dating, and other analyses of DNA sequence datasets from representatives of nearly all described species. To this end, we used both chloroplast (atpI\–atpH + rps16\–trnQ) and nuclear ribosomal (ITS + ETS) DNA sequences, as well as amplified fragment length polymorphisms (AFLPs). Our analyses showed that genus Myosotis likely arose in the Northern Hemisphere during the Miocene with the ancestor of the Southern Hemisphere lineage arising in the Pleistocene and radiating shortly thereafter. The Southern Hemisphere Myosotis species have very low levels of genetic divergence and their relationships are largely unresolved, likely due to a combination of recent radiation, hybridization, and incomplete lineage sorting. Our results are compared to those of similar studies on other New Zealand species radiations, and implications for ongoing and future Myosotis taxonomic and evolutionary research are discussed.

}, keywords = {AFLPs, DNA sequence markers, Molecular dating, molecular phylogeny, New Zealand, Species radiation}, isbn = {0378-2697}, doi = {10.1007/s00606-014-1166-x}, url = {http://dx.doi.org/10.1007/s00606-014-1166-x}, author = {Meudt, HeidiM. and Prebble, JessicaM. and Lehnebach, CarlosA.} } @article {91, title = {Acid-base balance in amphibian gastric mucosa.}, journal = {Am J Physiol}, volume = {229}, year = {1975}, month = {1975 Sep}, pages = {721-30}, abstract = {

It has been established that H+ secretion can be maintained in frog stomach in the absence of exogenous CO2 by using a nutrient bathing fluid containing 25 mM H2PO4 (pH approximately equal to 4.5) or by lowering the pH of a nonbuffered nutrient solution to about 3.0-3.6. Exogenous CO2 in the presence of these nutrient solutions uniformly caused a marked decrease in H+ secretion, PD, adn short-circuit current (Isc) and an increase in transmucosal resistance (R). Elevation of nutrient [k+] to 83 mM reduced R significantly but transiently without change in H+ when nutrient pH less than 5.0, whereas R returned to base line and H+ increased when nutrient pH greater than 5.0. Acidification of the nutrient medium in the presence of exogenous CO2 results in inhibition of the secretory pump, probably by decreasing intracellular pH, and also interferes with conductance at the nutrient membrane. Removal of exogenous CO2 from standard bicarbonate nutrient solution reduced by 50\% the H+, PD, and Isc without change in R; K+-free nutrient solutions reverse these changes in Isc and PD but not in H+. The dropping PD and rising R induced by K+-free nutrient solutions in 5\% CO2 - 95\% O2 are returned toward normal by 100\% O2. Our findings support an important role for exogenous CO2 in maintaining normal acid-base balance in frog mucosa by acting as an acidifying agent.

}, keywords = {Acid-Base Equilibrium, Animals, Anura, Bicarbonates, Carbon Dioxide, Electrophysiology, Gastric Mucosa, Hydrogen-Ion Concentration, Phosphates, Potassium, Rana catesbeiana, Solutions}, issn = {0002-9513}, author = {Silen, W and Machen, T E and Forte, J G} } @article {92, title = {Recombination of ciliary dynein of Tetrahymena with the outer fibers.}, journal = {J Biochem}, volume = {78}, year = {1975}, month = {1975 Jul}, pages = {41-9}, abstract = {

Recombination of ciliary dyneins of Tetrahymena pyriformis with the outer fibers was investigated using turbidimetry, co-sedimentation analysis and electron microscopy. As reported by Gibbons, 30S dynein could recombine with the outer fibers, while 14S dynein did to so a lesser extent. At acidic pH, however, most of the 14S dynein was also rebound to the outer fibers. When an excess of crude dynein fraction was added to the outer fiber fraction at pH 8.2, electron microscopic observations showed that the outer doublet microtubules were decorated not only with arms but also with other electron-dense materials. On the other hand, when crude dynein fraction was mixed with the outer fibers in an appropriate quantity, only arms were reconstituted at the regular positions of A-subfibers. ATP had an inhibitory effect on the recombination of dynein with the outer fibers.

}, keywords = {Adenosine Triphosphatases, Adenosine Triphosphate, Cilia, Flagella, Hydrogen-Ion Concentration, Magnesium, Microtubules, Nephelometry and Turbidimetry, Tetrahymena}, issn = {0021-924X}, author = {Shimizu, T} } @article {93, title = {Proceedings: The antimicrobial efficiencies of contact lens solutions.}, journal = {J Pharm Pharmacol}, volume = {27 Suppl?-2}, year = {1975}, month = {1975 Dec}, pages = {24P}, keywords = {Anti-Bacterial Agents, Contact Lenses, Ophthalmic Solutions, Pseudomonas aeruginosa, Staphylococcus aureus, Time Factors}, issn = {0022-3573}, author = {Davies, D J and Richardson, N E and Norton, D A and Meakin, B J} } @article {94, title = {Analysis of fatal blunt trauma presenting at an areawide trauma center.}, journal = {IMJ Ill Med J}, volume = {148}, year = {1975}, month = {1975 Nov}, pages = {511-5}, keywords = {Accidents, Traffic, Adolescent, Adult, Aged, Child, Preschool, Emergency Medical Services, Female, Humans, Illinois, Male, Middle Aged, Trauma Centers, Wounds, Nonpenetrating}, author = {Bartley, V H} } @article {95, title = {Atomic models for the polypeptide backbones of myohemerythrin and hemerythrin.}, journal = {Biochem Biophys Res Commun}, volume = {66}, year = {1975}, month = {1975 Oct 27}, pages = {1349-56}, keywords = {Animals, Cnidaria, Computers, Hemerythrin, Metalloproteins, Models, Molecular, Muscle Proteins, Protein Conformation, Species Specificity}, issn = {0006-291X}, author = {Hendrickson, W A and Ward, K B} } @article {96, title = {Digitoxin metabolism by rat liver microsomes.}, journal = {Biochem Pharmacol}, volume = {24}, year = {1975}, month = {1975 Sep 1}, pages = {1639-41}, keywords = {Animals, Chromatography, Thin Layer, Digitoxigenin, Digitoxin, Hydroxylation, In Vitro Techniques, Male, Microsomes, Liver, NADP, Rats, Time Factors}, issn = {0006-2952}, author = {Schmoldt, A and Benthe, H F and Haberland, G} } @article {97, title = {Studies on variant glucose-6-phosphate dehydrogenases: G6PD Fort Worth.}, journal = {Biochem Med}, volume = {13}, year = {1975}, month = {1975 Jul}, pages = {264-75}, keywords = {Adult, Drug Stability, Erythrocytes, Female, Genetic Variation, Glucosephosphate Dehydrogenase, Humans, Hydrogen-Ion Concentration, Kinetics, Male, Temperature, Texas}, issn = {0006-2944}, author = {Mills, G C and Alperin, J B and Trimmer, K B} } @article {98, title = {Denial of staff privileges upheld.}, journal = {Mod Healthc (Short Term Care)}, volume = {4}, year = {1975}, month = {1975 Dec}, pages = {64-5}, keywords = {Hospital Administration, Jurisprudence, Medical Staff, Hospital, United States}, issn = {0093-7061}, author = {Horty, J F} } @article {99, title = {Malathion A and B esterases of mouse liver-I.}, journal = {Biochem Pharmacol}, volume = {24}, year = {1975}, month = {1975 Sep 15}, pages = {1713-7}, keywords = {Animals, Drug Stability, Esterases, Female, Hydrogen-Ion Concentration, Liver, Malathion, Male, Metals, Mice, Sex Factors, Sulfhydryl Compounds}, issn = {0006-2952}, author = {Bhagwat, V M and Ramachandran, B V} } @article {100, title = {Rosette formation by mouse lymphocytes. IV. Fc and C3 receptors occurring together and separately on T cells and other leucocytes.}, journal = {Clin Exp Immunol}, volume = {19}, year = {1975}, month = {1975 Mar}, pages = {485-97}, abstract = {

A method is described for detecting the simultaneous presence of Fc and C3 receptors on mouse spleen cells. A proportion of both T cells and non-T cells bear both receptors. Both T-cell and non-T-cell Fc receptors were blocked by aggregated mouse IgG2 to the same degree. C3, but not Fc, receptors were blocked by factors present in the serum of irradiated mice or mice undergoing graft-versus-host reaction. Thymocytes activated by injection into irradiated F1 hybrid mice, and thymocytes regenerating after irradiation and bone marrow injection, appeared to have increased Fc receptors. A general role for Fc and C3 receptors in T cell-B cell co-operation is suggested.

}, keywords = {Animals, Binding Sites, Bone Marrow Cells, Bone Marrow Transplantation, Complement C3, Complement System Proteins, Female, Fluorescent Antibody Technique, Graft vs Host Reaction, Immune Adherence Reaction, Immunoglobulin Fc Fragments, Lymphocytes, Mice, Spleen, T-Lymphocytes, Thymus Gland, Transplantation, Homologous}, issn = {0009-9104}, author = {Gy{\"o}ngy{\"o}ssy, M I and Arnaiz-Villena, A and Soteriades-Vlachos, C and Playfair, J H} } @article {101, title = {Comparison between procaine and isocarboxazid metabolism in vitro by a liver microsomal amidase-esterase.}, journal = {Biochem Pharmacol}, volume = {24}, year = {1975}, month = {1975 Aug 15}, pages = {1517-21}, keywords = {Amidohydrolases, Animals, Esterases, Hydrogen-Ion Concentration, In Vitro Techniques, Isocarboxazid, Kinetics, Male, Metals, Microsomes, Liver, Phospholipids, Procaine, Proteins, Rats, Subcellular Fractions, Temperature}, issn = {0006-2952}, author = {Moroi, K and Sato, T} } @article {102, title = {Formate assay in body fluids: application in methanol poisoning.}, journal = {Biochem Med}, volume = {13}, year = {1975}, month = {1975 Jun}, pages = {117-26}, keywords = {Aldehyde Oxidoreductases, Animals, Body Fluids, Carbon Dioxide, Formates, Haplorhini, Humans, Hydrogen-Ion Concentration, Kinetics, Methanol, Methods, Pseudomonas}, issn = {0006-2944}, author = {Makar, A B and McMartin, K E and Palese, M and Tephly, T R} } @article {103, title = {Peptide-binding macromolecules in the blood of seriously ill or mentally retarded patients.}, journal = {J Lab Clin Med}, volume = {87}, year = {1976}, month = {1976 Feb}, pages = {299-319}, abstract = {

This report describes macromolecules that bind (des-aspartic acid1)-angiotensin II, the des aspartic acid1 derivative of angiotensin I, and several biologically active and inactive analogues of these polypeptides. The macromolecules were found in the plasma of approximately 2 per cent of ambulatory adults and hospitalized children and 32 per cent of the patients at two institutions for the mentally retarded. The binding properties of these macromolecules were studied by incubating with peptides labeled with 125iodine, and separating bound from free labeled peptide using small gel filtration columns. The peptide-binding macromolecules from several patients were compared. They showed very similar specificity for a group of arginyl peptides of the des-aspartyl1-angiotensin sequence. The plasma binders differed from one another in their optimum pH and their mobility in electrophoretic fields. Those with more acid pH optima displayed more rapid electrophoretic mobility. The binders fell into two classes based on apparent molecular weight, approximately 140,000 and 250,000. Those with the higher apparent molecular weight contained a large proportion of binder that could be precipitated with antiserum to human IgA. Kinetic measurements showed that the plasma binders were somewhat heterogeneous with respect to affinity for (des-asp1)-angiotensin, with apparent association constants ranging from 10(7) to 10(8) M-1. Binding activity was labile to heat, and to treatment with pepsin or trypsin. It was inhibited by calcium, protamine, streptomycin, and some other cationic compounds. The plasma peptide binder differed in specificity and molecular weight from soluble angiotensin-binding molecules extracted from tissues, and from properties expected of a receptor for angiotensin. These macromolecules may be useful reagents for measuring (des-asp1)-angiotensins. Their presence in plasma samples may interfere with angiotensin assays in some circumstances.

}, keywords = {Angiotensin II, Chromatography, Gel, Electrophoresis, Starch Gel, Humans, Hydrogen-Ion Concentration, Intellectual Disability, Kidney Failure, Chronic, Kinetics, Macromolecular Substances, Neoplasms, Osmolar Concentration, Peptides, Protein Binding, Saralasin}, issn = {0022-2143}, author = {Goodfriend, T L and Sindel, M and Fyhrquist, F and Hong, R and Azen, E and Stewart, J M} } @article {104, title = {The reaction of choline and 3,3-dimethyl-1-butanol with the acetylenzyme from acetylcholinesterase.}, journal = {J Neurochem}, volume = {25}, year = {1975}, month = {1975 Dec}, pages = {783-7}, keywords = {Acetylcholinesterase, Binding Sites, Choline, Hexanols, Hydrogen-Ion Concentration, Kinetics, Mathematics, Osmolar Concentration, Protein Binding, Sodium Chloride}, issn = {0022-3042}, author = {Dawson, R M} }