Magnetoreception System in Honeybees (Apis mellifera)
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{"title"=>"Magnetoreception System in Honeybees (Apis mellifera)", "type"=>"journal", "authors"=>[{"first_name"=>"Chin-Yuan", "last_name"=>"Hsu"}, {"first_name"=>"Fu-Yao", "last_name"=>"Ko"}, {"first_name"=>"Chia-Wei", "last_name"=>"Li"}, {"first_name"=>"Kuni", "last_name"=>"Fann"}, {"first_name"=>"Juh-Tzeng", "last_name"=>"Lue"}], "year"=>2007, "source"=>"PLoS ONE", "identifiers"=>{"pmid"=>"17460762", "isbn"=>"1932-6203 (Electronic) 1932-6203 (Linking)", "doi"=>"10.1371/journal.pone.0000395", "issn"=>"1932-6203"}, "id"=>"b7699ef9-a736-3b75-ab39-b66f5c42fa69", "abstract"=>"Honeybees (Apis mellifera) undergo iron biomineralization, providing the basis for magnetoreception. We showed earlier the presence of superparamagnetic magnetite in iron granules formed in honeybees, and subscribed to the notion that external magnetic fields may cause expansion or contraction of the superparamagnetic particles in an orientation-specific manner, relaying the signal via cytoskeleton (Hsu and Li 1994). In this study, we established a size-density purification procedure, with which quantitative amount of iron granules was obtained from honey bee trophocytes and characterized; the density of iron granules was determined to be 1.25 g/cm(3). While we confirmed the presence of superparamagnetic magnetite in the iron granules, we observed changes in the size of the magnetic granules in the trophycytes upon applying additional magnetic field to the cells. A concomitant release of calcium ion was observed by confocal microscope. This size fluctuation triggered the increase of intracellular Ca(+2) , which was inhibited by colchicines and latrunculin B, known to be blockers for microtubule and microfilament syntheses, respectively. The associated cytoskeleton may thus relay the magnetosignal, initiating a neural response. A model for the mechanism of magnetoreception in honeybees is proposed, which may be applicable to most, if not all, magnetotactic organisms.", "link"=>"http://www.mendeley.com/research/magnetoreception-system-honeybees-apis-mellifera", "reader_count"=>97, "reader_count_by_academic_status"=>{"Unspecified"=>3, "Professor > Associate Professor"=>4, "Librarian"=>3, "Researcher"=>23, "Student > Doctoral Student"=>4, "Student > Ph. D. Student"=>27, "Student > Postgraduate"=>3, "Student > Master"=>8, "Other"=>4, "Student > Bachelor"=>11, "Professor"=>6}, "reader_count_by_user_role"=>{"Unspecified"=>3, "Professor > Associate Professor"=>4, "Librarian"=>3, "Researcher"=>23, "Student > Doctoral Student"=>4, "Student > Ph. D. Student"=>27, "Student > Postgraduate"=>3, "Student > Master"=>8, "Other"=>4, "Student > Bachelor"=>11, "Professor"=>6}, "reader_count_by_subject_area"=>{"Engineering"=>6, "Unspecified"=>6, "Environmental Science"=>3, "Biochemistry, Genetics and Molecular Biology"=>2, "Agricultural and Biological Sciences"=>67, "Medicine and Dentistry"=>1, "Arts and Humanities"=>1, "Neuroscience"=>1, "Physics and Astronomy"=>2, "Chemistry"=>4, "Social Sciences"=>1, "Earth and Planetary Sciences"=>2}, "reader_count_by_subdiscipline"=>{"Engineering"=>{"Engineering"=>6}, "Medicine and Dentistry"=>{"Medicine and Dentistry"=>1}, "Neuroscience"=>{"Neuroscience"=>1}, "Chemistry"=>{"Chemistry"=>4}, "Social Sciences"=>{"Social Sciences"=>1}, "Physics and Astronomy"=>{"Physics and Astronomy"=>2}, "Earth and Planetary Sciences"=>{"Earth and Planetary Sciences"=>2}, "Agricultural and Biological Sciences"=>{"Agricultural and Biological Sciences"=>67}, "Biochemistry, Genetics and Molecular Biology"=>{"Biochemistry, Genetics and Molecular Biology"=>2}, "Unspecified"=>{"Unspecified"=>6}, "Environmental Science"=>{"Environmental Science"=>3}, "Arts and Humanities"=>{"Arts and Humanities"=>1}}, "reader_count_by_country"=>{"Argentina"=>1, "United States"=>4, "China"=>1, "Brazil"=>1, "Germany"=>2}, "group_count"=>3}

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Figshare

  • {"files"=>["https://ndownloader.figshare.com/files/950361"], "description"=>"<p>A flow diagram showing the purification processes of the size-density purification technique.</p>", "links"=>[], "tags"=>["biophysics/biomacromolecule-ligand interactions", "biophysics/cell signaling and trafficking structures", "cell biology/cell signaling", "cell biology/chemical biology of the cell", "cell biology/cytoskeleton"], "article_id"=>620680, "categories"=>["Biophysics", "Cell Biology"], "users"=>["Chin-Yuan Hsu", "Fu-Yao Ko", "Chia-Wei Li", "Kuni Fann", "Juh-Tzeng Lue"], "doi"=>"https://dx.doi.org/10.1371/journal.pone.0000395.g001", "stats"=>{"downloads"=>2, "page_views"=>9, "likes"=>0}, "figshare_url"=>"https://figshare.com/articles/_Figure_1_/620680", "title"=>"Figure 1", "pos_in_sequence"=>0, "defined_type"=>1, "published_date"=>"2013-02-21 12:32:00"}
  • {"files"=>["https://ndownloader.figshare.com/files/950462"], "description"=>"<p>IGs purified from the trophocytes of honeybees. (A) A large amount of IGs appear in precipitates purified from the trophocytes. Scale bar, 1 µm. (B) Purified IGs enclosed with lipid-bilayer membranes (arrowhead). Scale bar, 100 nm. (C) EDX spectrum is obtained from an IG in the purified precipitates. Iron (Fe), calcium (Ca) and phosphorus (P) are present in an IG. STEM mode of 100-kV accelerating voltage was used; counts were made for 100 seconds. (D) EDX spectrum of spurr's resin is devoid of IGs in the purified precipitates. The experimental conditions are the same as in C. (E) Size distribution of purified IGs calculated from the TEM pictures (N = 274). N, total number of granules used in this calculation.</p>", "links"=>[], "tags"=>["biophysics/biomacromolecule-ligand interactions", "biophysics/cell signaling and trafficking structures", "cell biology/cell signaling", "cell biology/chemical biology of the cell", "cell biology/cytoskeleton"], "article_id"=>620780, "categories"=>["Biophysics", "Cell Biology"], "users"=>["Chin-Yuan Hsu", "Fu-Yao Ko", "Chia-Wei Li", "Kuni Fann", "Juh-Tzeng Lue"], "doi"=>"https://dx.doi.org/10.1371/journal.pone.0000395.g002", "stats"=>{"downloads"=>1, "page_views"=>7, "likes"=>0}, "figshare_url"=>"https://figshare.com/articles/_Figure_2_/620780", "title"=>"Figure 2", "pos_in_sequence"=>0, "defined_type"=>1, "published_date"=>"2013-02-21 12:32:39"}
  • {"files"=>["https://ndownloader.figshare.com/files/950829"], "description"=>"<p>The resonance linewidth and anisotropy fields of the broad resonance lines (HF) of purified IGs. (A) Temperature dependence of the resonance linewidth of the HF. The solid line is the best fit of the HF data according to Eq. 1, with Δ<i>H</i><sup>0</sup> = 1791±37 Oe and Δ<i>E</i>/2<i>k</i><sub>B</sub> = 50.8±2.6 K. (B) Temperature dependence of the resonance field of HF and LF. Note that the HF and LF curves are almost parallel to each other, with the field shifting by an average value of about 2496±50 Oe. (C) Anisotropy fields calculated from the resonant field's values, using Eq. 2 for the HF lines.</p>", "links"=>[], "tags"=>["biophysics/biomacromolecule-ligand interactions", "biophysics/cell signaling and trafficking structures", "cell biology/cell signaling", "cell biology/chemical biology of the cell", "cell biology/cytoskeleton"], "article_id"=>621147, "categories"=>["Biophysics", "Cell Biology"], "users"=>["Chin-Yuan Hsu", "Fu-Yao Ko", "Chia-Wei Li", "Kuni Fann", "Juh-Tzeng Lue"], "doi"=>"https://dx.doi.org/10.1371/journal.pone.0000395.g006", "stats"=>{"downloads"=>1, "page_views"=>3, "likes"=>0}, "figshare_url"=>"https://figshare.com/articles/_Figure_6_/621147", "title"=>"Figure 6", "pos_in_sequence"=>0, "defined_type"=>1, "published_date"=>"2013-02-21 12:34:57"}
  • {"files"=>["https://ndownloader.figshare.com/files/950911"], "description"=>"<p>The magnetic map hypothesis of magnetoreception for orientation and positioning during foraging and homing. (A) When honeybees fly in the direction paralleled to external magnetic field, MG expands due to the repellent force of SM. When honeybees fly in the perpendicular direction to external magnetic field, MG contracts in the same direction due to the attractive force of SM. (B) The direction of magnetic field of SM is parallel to the direction of Earth's magnetic field at flower 1. SM would be in a side-by-side position, creating repulsion and subsequent expansion of the MGs. At the flower 3, the direction of magnetic field of SM is vertical to the direction of Earth's magnetic field. SM would be positioned end-to-end, creating attraction and subsequent contraction of the MGs. This contraction induces the tensing of cytoskeletons and triggers the increase of [Ca<sup>+2</sup>]i in trophocytes. At flower 2, the relaxing and tensing of cytoskeletons is a mixture of flower 1 and flower 3. The direction of magnetic field of SM at the flower 1 is the same as flower 5. Flower 2 is the same as flower 6, and so on. The distinction in both cases is dependent on the direction of waggle dance.</p>", "links"=>[], "tags"=>["biophysics/biomacromolecule-ligand interactions", "biophysics/cell signaling and trafficking structures", "cell biology/cell signaling", "cell biology/chemical biology of the cell", "cell biology/cytoskeleton"], "article_id"=>621228, "categories"=>["Biophysics", "Cell Biology"], "users"=>["Chin-Yuan Hsu", "Fu-Yao Ko", "Chia-Wei Li", "Kuni Fann", "Juh-Tzeng Lue"], "doi"=>"https://dx.doi.org/10.1371/journal.pone.0000395.g007", "stats"=>{"downloads"=>0, "page_views"=>4, "likes"=>0}, "figshare_url"=>"https://figshare.com/articles/_Figure_7_/621228", "title"=>"Figure 7", "pos_in_sequence"=>0, "defined_type"=>1, "published_date"=>"2013-02-21 12:35:24"}
  • {"files"=>["https://ndownloader.figshare.com/files/950750"], "description"=>"<p>The images of increase of [Ca<sup>+2</sup>]i in the live trophocytes obtained by confocal microscope. (A) The image of trophocytes and fat cells under confocal microscope. Trophocytes (arrowhead). Fat cells (arrow). Scale bar, 40 µm. (B) The image of trophocytes and fat cells labeled fluo 4 under confocal microscope. Trophocytes (arrowhead). Fat cells (arrow). Scale bar, 40 µm. (C) The merge of Figure A and Figure B. Scale bar, 40 µm. (D) The fluorescence intensity of trophocytes (○), fat cells (Δ), and trophocytes and fat cells together (□) with 1 Gauss magnetic field. The fluorescence intensity of trophocytes (•), fat cells (▴) and trophocytes and fat cells together (▪) without 1 Gauss magnetic field as control. (E) The fluorescence intensity of trophocytes (○), fat cells (Δ), and trophocytes and fat cells together (□), which is inhibited by colchicine and with 1 Gauss magnetic field. The fluorescence intensity of trophocytes (•), fat cells (▴) and trophocytes and fat cells together (▪), which is inhibited by colchicine without 1 Gauss magnetic field as control. (F) The fluorescence intensity of trophocytes (○), fat cells (Δ), and trophocytes and fat cells together (□), which is inhibited by latrunculin B and with 1 Gauss magnetic field. The fluorescence intensity of trophocytes (•), fat cells (▴) and trophocytes and fat cells together (▪), which is inhibited by latrunculin B without 1 Gauss magnetic field as control.</p>", "links"=>[], "tags"=>["biophysics/biomacromolecule-ligand interactions", "biophysics/cell signaling and trafficking structures", "cell biology/cell signaling", "cell biology/chemical biology of the cell", "cell biology/cytoskeleton"], "article_id"=>621069, "categories"=>["Biophysics", "Cell Biology"], "users"=>["Chin-Yuan Hsu", "Fu-Yao Ko", "Chia-Wei Li", "Kuni Fann", "Juh-Tzeng Lue"], "doi"=>"https://dx.doi.org/10.1371/journal.pone.0000395.g005", "stats"=>{"downloads"=>1, "page_views"=>7, "likes"=>0}, "figshare_url"=>"https://figshare.com/articles/_Figure_5_/621069", "title"=>"Figure 5", "pos_in_sequence"=>0, "defined_type"=>1, "published_date"=>"2013-02-21 12:34:25"}
  • {"files"=>["https://ndownloader.figshare.com/files/950576"], "description"=>"<p>The magnetic properties of IGs determined by magnetic-determining techniques. (A) An averaged magnetization curve of SQUID from the purified IGs at 300°K for six runs. (B) An image of AFM from one of the purified IGs. (C) An image of MFM from one of the purified IGs. (D) A spectrum of ESCA from the purified IGs. The left thin line shows the Fe(2p1/2) of FeOOH. The middle thin line shows the Fe(2p3/2) of Fe2O3. The right thin line shows the Fe(2p1/2) of FeO. (E) A photoelectron spectrum of elemental composition of ESCA from the purified IGs. (F) Typical X-band resonance spectra from the purified IGs at different temperatures. Right inset shows a magnified image from the arrow. Left inset shows a magnified image from the arrowhead.</p>", "links"=>[], "tags"=>["biophysics/biomacromolecule-ligand interactions", "biophysics/cell signaling and trafficking structures", "cell biology/cell signaling", "cell biology/chemical biology of the cell", "cell biology/cytoskeleton"], "article_id"=>620894, "categories"=>["Biophysics", "Cell Biology"], "users"=>["Chin-Yuan Hsu", "Fu-Yao Ko", "Chia-Wei Li", "Kuni Fann", "Juh-Tzeng Lue"], "doi"=>"https://dx.doi.org/10.1371/journal.pone.0000395.g003", "stats"=>{"downloads"=>1, "page_views"=>7, "likes"=>0}, "figshare_url"=>"https://figshare.com/articles/_Figure_3_/620894", "title"=>"Figure 3", "pos_in_sequence"=>0, "defined_type"=>1, "published_date"=>"2013-02-21 12:33:17"}
  • {"files"=>["https://ndownloader.figshare.com/files/950655"], "description"=>"<p>The images of MGs in the trophocytes obtained by confocal microscope. (A) MGs (arrowhead) appear as tiny black particles under low magnification in the live trophocytes. Arrow indicates oil body. Scale bar, 8 µm. (B) MGs (arrowhead) appear as black granules under high magnification in the live trophocytes. The images of MGs are obtained without the application of 1 Gauss magnetic field. Arrow indicates oil body. Inset shows a magnified MG. Scale bar, 1 µm. (C) The same images obtained by the application of 1 Gauss magnetic field in the live trophocytes. White arrow indicates the direction of magnetic field. Arrowhead indicates MGs. Arrow indicates oil body. Inset shows a magnified MG. Scale bar, 1 µm. (D) MGs (arrowhead) appear as tiny black particles under low magnification in the dead trophocytes. Scale bar, 8 µm. (E) MGs (arrowhead) appear as black granules under high magnification in the dead trophocytes. The images of MGs are obtained without the application of 1 Gauss magnetic field. Inset shows a magnified MG. Scale bar, 1 µm. (F) The same images obtained by the application of 1 Gauss magnetic field in the dead trophocytes. Arrowhead indicates MGs. White arrow indicates the direction of magnetic field. Inset shows a magnified MG. Scale bar, 1 µm.</p>", "links"=>[], "tags"=>["biophysics/biomacromolecule-ligand interactions", "biophysics/cell signaling and trafficking structures", "cell biology/cell signaling", "cell biology/chemical biology of the cell", "cell biology/cytoskeleton"], "article_id"=>620975, "categories"=>["Biophysics", "Cell Biology"], "users"=>["Chin-Yuan Hsu", "Fu-Yao Ko", "Chia-Wei Li", "Kuni Fann", "Juh-Tzeng Lue"], "doi"=>"https://dx.doi.org/10.1371/journal.pone.0000395.g004", "stats"=>{"downloads"=>1, "page_views"=>17, "likes"=>0}, "figshare_url"=>"https://figshare.com/articles/_Figure_4_/620975", "title"=>"Figure 4", "pos_in_sequence"=>0, "defined_type"=>1, "published_date"=>"2013-02-21 12:33:50"}

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Relative Metric

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