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      <qbo:mapNotes xmlns:qbo="https://dr-richard-barker.github.io/quantum-biology-atlas/qbo/1.0">Seed germination before photosynthesis. Before chloroplasts mature, an oilseed embryo is entirely heterotrophic: stored triacylglycerol must be mobilised, run through peroxisomal beta-oxidation and the glyoxylate cycle, and converted to ATP by mitochondrial respiration. That makes the first 0-72 hours after imbibition the window where a respiratory or Fe/S lesion would have most leverage, and the reason Arabidopsis and Brassica are comparable systems for the review's argument. The original Figure 6 carried a summary table of "normalized trend ranges" for germination rate, radicle length, ATP status and seedling vigour; those were qualitative cross-study impressions rather than measured values, so no number from them is reproduced here. The map shows the route and the endpoints; any quantity has to arrive from projected data. Every node on this map is T3 or T4, which is the honest state of the field: the review's central proposal is a geomagnetic-versus-near-null imbibition time course, and no such experiment exists in its bibliography. Derived from: Figure 6 of Porterfield &amp; Barker, "Plant Responses to Near-Null Magnetic Fields" — expanded to the reserve-mobilisation route and bound to Arabidopsis loci</qbo:mapNotes>
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    <glyph id="peroxisome" class="compartment">
      <label text="Peroxisome" />
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    <glyph id="mitochondrial_matrix" class="compartment">
      <label text="Mitochondrial matrix" />
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    <glyph id="cell" class="compartment">
      <label text="Cell" />
      <bbox x="43.39" y="261.68" w="558.79" h="99.44" />
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    <glyph id="organism" class="compartment">
      <label text="Organism" />
      <bbox x="223.33" y="399.12" w="198.90" h="86.64" />
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    <glyph id="TAG_LIPASE" class="macromolecule" compartmentRef="peroxisome">
      <label text="TAG lipase (SDP1)" />
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        <label text="oil body" />
        <bbox x="92.24" y="-2.60" w="56.00" h="16.00" />
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      <extension>
        <qbo:annotation xmlns:qbo="https://dr-richard-barker.github.io/quantum-biology-atlas/qbo/1.0" entity="QBO:TAG_LIPASE" evidenceTier="T4" confidence="inferred">
          <qbo:quantumClass>structural_context</qbo:quantumClass>
          <qbo:xref db="ec">3.1.1.3</qbo:xref>
        </qbo:annotation>
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    <glyph id="BETA_OXIDATION" class="process" compartmentRef="peroxisome">
      <label text="Beta-oxidation" />
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        <label text="H2O2 by design" />
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      <extension>
        <qbo:annotation xmlns:qbo="https://dr-richard-barker.github.io/quantum-biology-atlas/qbo/1.0" entity="QBO:BETA_OXIDATION" evidenceTier="T3" confidence="inferred">
          <qbo:quantumClass>ros_leak_site</qbo:quantumClass>
          <qbo:xref db="ec">1.3.3.6</qbo:xref>
          <qbo:rationale>Acyl-CoA oxidase is a flavoprotein that reduces O2 directly to H2O2 as part of its normal catalytic cycle — one of the few places in the cell where peroxide production is the intended chemistry rather than a leak. During germination that makes the peroxisome a major ROS source at exactly the stage the review argues matters most.
</qbo:rationale>
          <qbo:caveat>A flavin semiquinone is not well established in the acyl-CoA oxidase mechanism, and the enzyme's own catalase-rich compartment quenches the product quickly. Classed only as a ROS source, not as a radical-pair site.
</qbo:caveat>
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    <glyph id="GLYOXYLATE_CYCLE" class="complex" compartmentRef="peroxisome">
      <label text="Glyoxylate cycle" />
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      <glyph id="GLYOXYLATE_CYCLE__u0" class="unit of information">
        <label text="ICL / MLS" />
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      <extension>
        <qbo:annotation xmlns:qbo="https://dr-richard-barker.github.io/quantum-biology-atlas/qbo/1.0" entity="QBO:GLYOXYLATE_CYCLE" evidenceTier="T4" confidence="verified">
          <qbo:quantumClass>structural_context</qbo:quantumClass>
          <qbo:xref db="agi">AT3G21720</qbo:xref>
          <qbo:xref db="agi">AT5G03860</qbo:xref>
          <qbo:xref db="ec">4.1.3.1</qbo:xref>
          <qbo:xref db="ec">2.3.3.9</qbo:xref>
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    <glyph id="ACETYL_COA" class="simple chemical" compartmentRef="mitochondrial_matrix">
      <label text="Acetyl-CoA" />
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      <extension>
        <qbo:annotation xmlns:qbo="https://dr-richard-barker.github.io/quantum-biology-atlas/qbo/1.0" entity="QBO:ACETYL_COA" evidenceTier="T4" confidence="verified">
          <qbo:quantumClass>structural_context</qbo:quantumClass>
          <qbo:xref db="chebi">CHEBI:15351</qbo:xref>
          <qbo:xref db="kegg">C00024</qbo:xref>
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    <glyph id="COMPLEX_I" class="complex">
      <label text="Complex I" />
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        <label text="FMN" />
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      <glyph id="COMPLEX_I__u1" class="unit of information">
        <label text="8 × Fe/S" />
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      <extension>
        <qbo:annotation xmlns:qbo="https://dr-richard-barker.github.io/quantum-biology-atlas/qbo/1.0" entity="QBO:COMPLEX_I" evidenceTier="T3" confidence="inferred">
          <qbo:quantumClass>flavin_semiquinone</qbo:quantumClass>
          <qbo:quantumClass>iron_sulfur_4Fe4S</qbo:quantumClass>
          <qbo:quantumClass>iron_sulfur_2Fe2S</qbo:quantumClass>
          <qbo:quantumClass>ros_leak_site</qbo:quantumClass>
          <qbo:nucleus>1H</qbo:nucleus>
          <qbo:nucleus>14N</qbo:nucleus>
          <qbo:nucleus>57Fe</qbo:nucleus>
          <qbo:nucleus>33S</qbo:nucleus>
          <qbo:cofactor>CHEBI:58210</qbo:cofactor>
          <qbo:xref db="agi">AT5G37510</qbo:xref>
          <qbo:xref db="agi">AT5G08530</qbo:xref>
          <qbo:xref db="agi">AT4G02580</qbo:xref>
          <qbo:xref db="agi">AT5G11770</qbo:xref>
          <qbo:xref db="go_component">GO:0005747</qbo:xref>
          <qbo:xref db="ec">7.1.1.2</qbo:xref>
          <qbo:rationale>The FMN site forms a flavin semiquinone during turnover and is a known superoxide-producing leak site, and the Fe/S chain performs sequential one-electron transfers — both of the physical routes the radical-pair and hyperfine arguments require. No published experiment has applied a near-null field and measured plant complex I activity, so this is a hypothesis with a mechanism, not a result.
</qbo:rationale>
          <qbo:caveat>Electron transfer along the Fe/S chain is fast relative to plausible singlet-triplet mixing times, so a coherent radical-pair effect here is harder to argue than at the flavin. Treat the flavin and the cluster chain as separate hypotheses rather than one.
</qbo:caveat>
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      <label text="Complex IV (COX)" />
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        <label text="heme a3 / CuB" />
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      <extension>
        <qbo:annotation xmlns:qbo="https://dr-richard-barker.github.io/quantum-biology-atlas/qbo/1.0" entity="QBO:COMPLEX_IV" evidenceTier="T3" confidence="inferred">
          <qbo:quantumClass>heme_copper_binuclear</qbo:quantumClass>
          <qbo:quantumClass>cu_a_binuclear</qbo:quantumClass>
          <qbo:quantumClass>heme_electron_carrier</qbo:quantumClass>
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          <qbo:nucleus>1H</qbo:nucleus>
          <qbo:xref db="go_component">GO:0005751</qbo:xref>
          <qbo:xref db="ec">7.1.1.9</qbo:xref>
          <qbo:rationale>The review names cytochrome oxidase explicitly as a candidate direct metabolic target. The heme a3/CuB centre passes through paramagnetic oxygen intermediates (P, F, oxoferryl) whose spin states are, in principle, field-addressable.
</qbo:rationale>
          <qbo:caveat>Strongly exchange-coupled metal centres relax very fast, which argues against coherent spin effects. This is a mechanistically attractive but physically demanding hypothesis, and is labelled T3 for that reason.
</qbo:caveat>
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    <glyph id="ACONITASE" class="macromolecule" compartmentRef="mitochondrial_matrix">
      <label text="Aconitase" />
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        <label text="4Fe-4S sentinel" />
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      <extension>
        <qbo:annotation xmlns:qbo="https://dr-richard-barker.github.io/quantum-biology-atlas/qbo/1.0" entity="QBO:ACONITASE" evidenceTier="T3" confidence="inferred">
          <qbo:quantumClass>iron_sulfur_4Fe4S</qbo:quantumClass>
          <qbo:nucleus>57Fe</qbo:nucleus>
          <qbo:nucleus>33S</qbo:nucleus>
          <qbo:xref db="agi">AT4G35830</qbo:xref>
          <qbo:xref db="agi">AT4G26970</qbo:xref>
          <qbo:xref db="agi">AT2G05710</qbo:xref>
          <qbo:xref db="ec">4.2.1.3</qbo:xref>
          <qbo:rationale>The review nominates aconitase as the sentinel of Fe/S integrity, and the biochemistry supports it: the exposed cluster iron makes aconitase the first TCA activity to fall under oxidative stress, so it reports cluster damage before anything else does.
</qbo:rationale>
          <qbo:caveat>Precisely because aconitase responds to any oxidative insult, a change under NNMF would NOT by itself implicate a magnetic mechanism. It is a sensitive readout and a poor discriminator; it needs a paired ROS-independent control.
</qbo:caveat>
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    <glyph id="GERMINATION_ATP" class="simple chemical" compartmentRef="cell">
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        <label text="the missing measurement" />
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      <extension>
        <qbo:annotation xmlns:qbo="https://dr-richard-barker.github.io/quantum-biology-atlas/qbo/1.0" entity="QBO:GERMINATION_ATP" evidenceTier="T4" confidence="reported">
          <qbo:quantumClass>structural_context</qbo:quantumClass>
          <qbo:xref db="chebi">CHEBI:30616</qbo:xref>
          <qbo:xref db="chebi">CHEBI:456216</qbo:xref>
          <qbo:xref db="kegg">C00002</qbo:xref>
          <qbo:xref db="kegg">C00008</qbo:xref>
          <qbo:evidence ref="Nietzel2020" doi="10.1073/pnas.1910501117" direction="increase">Mitochondrial energy metabolism is redox-kick-started during seed germination, establishing that respiratory competence is restored before photosynthesis.
</qbo:evidence>
          <qbo:evidence ref="Rosental2014" doi="10.1017/S0960258513000391" direction="increase">Primary metabolism is activated and regulated during seed germination, with respiration supplying the energy for reserve mobilisation and cell expansion.
</qbo:evidence>
        </qbo:annotation>
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    <glyph id="MITO_SUPEROXIDE" class="simple chemical" compartmentRef="mitochondrial_matrix">
      <label text="ROS signalling window" />
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      <glyph id="MITO_SUPEROXIDE__u0" class="unit of information">
        <label text="too little / too much" />
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      <extension>
        <qbo:annotation xmlns:qbo="https://dr-richard-barker.github.io/quantum-biology-atlas/qbo/1.0" entity="QBO:MITO_SUPEROXIDE" evidenceTier="T2" confidence="reported">
          <qbo:quantumClass>ros_leak_site</qbo:quantumClass>
          <qbo:xref db="chebi">CHEBI:18421</qbo:xref>
          <qbo:xref db="chebi">CHEBI:16240</qbo:xref>
          <qbo:xref db="agi">AT3G10920</qbo:xref>
          <qbo:evidence ref="Parmagnani2022" doi="10.3390/biom12121824" direction="altered" fieldRegime="NNMF">Near-null magnetic field exposure alters ROS-associated transcriptomic and metabolomic programmes in Arabidopsis.
</qbo:evidence>
          <qbo:evidence ref="Farooq2021" doi="10.3389/fpls.2021.781734" direction="altered">Reactive oxygen species and mitochondria jointly regulate seed germination, establishing the route from mitochondrial ROS to a developmental outcome.
</qbo:evidence>
          <qbo:rationale>Not a magnetosensitive mechanism itself — it is the amplifier. A field effect too small to measure as a rate change can still register here, because ROS signalling is threshold-like.
</qbo:rationale>
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      <label text="Cytochrome c" />
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        <label text="→ ABI4 / ABA" />
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      <extension>
        <qbo:annotation xmlns:qbo="https://dr-richard-barker.github.io/quantum-biology-atlas/qbo/1.0" entity="QBO:CYTOCHROME_C" evidenceTier="T3" confidence="inferred">
          <qbo:quantumClass>heme_electron_carrier</qbo:quantumClass>
          <qbo:nucleus>57Fe</qbo:nucleus>
          <qbo:nucleus>1H</qbo:nucleus>
          <qbo:xref db="agi">AT1G22840</qbo:xref>
          <qbo:xref db="agi">AT4G10040</qbo:xref>
          <qbo:xref db="go_component">GO:0005758</qbo:xref>
          <qbo:evidence ref="Racca2022" doi="10.1111/nph.18287" direction="altered">Cytochrome c and the transcription factor ABI4 link mitochondrial status to ABA-dependent seed germination.
</qbo:evidence>
          <qbo:rationale>A one-electron heme carrier, paramagnetic in the ferric state. Included because Racca et al. place cytochrome c on the path from mitochondrial state to germination timing, which is the developmental window the review argues matters most.
</qbo:rationale>
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      <label text="Radicle emergence" />
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        <label text="0–72 h endpoint" />
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      <extension>
        <qbo:annotation xmlns:qbo="https://dr-richard-barker.github.io/quantum-biology-atlas/qbo/1.0" entity="QBO:RADICLE_EMERGENCE" evidenceTier="T4" confidence="reported">
          <qbo:quantumClass>structural_context</qbo:quantumClass>
          <qbo:evidence ref="Farooq2021" doi="10.3389/fpls.2021.781734" direction="altered">Reactive oxygen species and mitochondria jointly regulate seed germination, defining the window in which a respiratory lesion would have most leverage.
</qbo:evidence>
          <qbo:evidence ref="Eckardt2005" doi="10.1105/tpc.105.034843" direction="altered">Peroxisomal citrate synthase provides the exit route from fatty acid metabolism in oilseeds, linking reserve mobilisation to the TCA cycle.
</qbo:evidence>
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      <extension>
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      <extension>
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        <label text="via citrate" />
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      <extension>
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        <label text="via NADH" />
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      <extension>
        <qbo:edgeClass xmlns:qbo="https://dr-richard-barker.github.io/quantum-biology-atlas/qbo/1.0">indirect_influence</qbo:edgeClass>
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      <extension>
        <qbo:edgeClass xmlns:qbo="https://dr-richard-barker.github.io/quantum-biology-atlas/qbo/1.0">electron_transfer</qbo:edgeClass>
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      <extension>
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        <label text="leak" />
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      <extension>
        <qbo:edgeClass xmlns:qbo="https://dr-richard-barker.github.io/quantum-biology-atlas/qbo/1.0">direct_influence</qbo:edgeClass>
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    </arc>
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      <extension>
        <qbo:edgeClass xmlns:qbo="https://dr-richard-barker.github.io/quantum-biology-atlas/qbo/1.0">electron_transfer</qbo:edgeClass>
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    </arc>
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      <glyph id="arc10__lbl" class="annotation">
        <label text="ABI4 / ABA" />
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      <extension>
        <qbo:edgeClass xmlns:qbo="https://dr-richard-barker.github.io/quantum-biology-atlas/qbo/1.0">hormonal_feedback</qbo:edgeClass>
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        <label text="sets the pace" />
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      <extension>
        <qbo:edgeClass xmlns:qbo="https://dr-richard-barker.github.io/quantum-biology-atlas/qbo/1.0">energy_feedback</qbo:edgeClass>
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    <arc id="arc12" class="modulation" source="MITO_SUPEROXIDE" target="RADICLE_EMERGENCE">
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        <label text="signalling window" />
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      <extension>
        <qbo:edgeClass xmlns:qbo="https://dr-richard-barker.github.io/quantum-biology-atlas/qbo/1.0">redox_feedback</qbo:edgeClass>
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    </arc>
    <arc id="arc13" class="modulation" source="MITO_SUPEROXIDE" target="ACONITASE">
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      <glyph id="arc13__lbl" class="annotation">
        <label text="cluster damage" />
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      <extension>
        <qbo:edgeClass xmlns:qbo="https://dr-richard-barker.github.io/quantum-biology-atlas/qbo/1.0">redox_feedback</qbo:edgeClass>
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    </arc>
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        <label text="TCA flux" />
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      <extension>
        <qbo:edgeClass xmlns:qbo="https://dr-richard-barker.github.io/quantum-biology-atlas/qbo/1.0">indirect_influence</qbo:edgeClass>
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  </map>
</sbgn>