<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">AJPS</journal-id><journal-title-group><journal-title>American Journal of Plant Sciences</journal-title></journal-title-group><issn pub-type="epub">2158-2742</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ajps.2023.142009</article-id><article-id pub-id-type="publisher-id">AJPS-122967</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Biomedical&amp;Life Sciences</subject></subj-group></article-categories><title-group><article-title>
 
 
  Comparing Durations of Plant and Human Physiological Processes and Highlighting Their Importance to the Earth System
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Ashehad</surname><given-names>A. Ali</given-names></name><xref ref-type="aff" rid="aff1"><sub>1</sub></xref></contrib></contrib-group><aff id="aff1"><label>1</label><addr-line>Department of Bioclimatology, University of G&amp;amp;#246;ttingen, G&amp;amp;#246;ttingen, Germany</addr-line></aff><pub-date pub-type="epub"><day>09</day><month>02</month><year>2023</year></pub-date><volume>14</volume><issue>02</issue><fpage>113</fpage><lpage>117</lpage><history><date date-type="received"><day>10,</day>	<month>December</month>	<year>2022</year></date><date date-type="rev-recd"><day>7,</day>	<month>February</month>	<year>2023</year>	</date><date date-type="accepted"><day>10,</day>	<month>February</month>	<year>2023</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Highly dynamic physiology limits our ability to understand and compare durations of plant physiological and human physiological processes in concert. In this study, I used literature data and examined a reproductive process, fruiting, for deciduous rubber trees from two tropical rubber plantations grown in different geographical locations. In particular, I focused on fruiting timings and found that fruiting in rubber trees occurs within eight to nine months from the time when the rubber tree is dormant. The duration of this interesting physiological process is analogous to a situation, where women take about nine months to deliver a baby following fertilization. Based on the data, I generalize (“extrapolate”) that every deciduous tree fruiting takes about eight to nine months since it is dormant. I recommend that the fruiting process be represented in earth system models for deciduous trees. I also suggest follow-up work that can be done in this field of research.
 
</p></abstract><kwd-group><kwd>Plant Physiology</kwd><kwd> Human Physiology</kwd><kwd> Fruiting</kwd><kwd> Deciduous Trees</kwd><kwd> Earth System Models</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Plants are invaluable and extraordinary in that they can turn sunlight’s energy into food [e.g., [<xref ref-type="bibr" rid="scirp.122967-ref1">1</xref>] ], which we humans cannot do. In general, appreciating this fact and communicating this fact to non-plant scientists takes a lot of work. The non-plant community often thinks it is a well-known process and thus has been well documented and quantified, which is not true. Plants provide many services to humans (including animals), such as oxygen [<xref ref-type="bibr" rid="scirp.122967-ref2">2</xref>] , food, and shelter. In contrast, humans provide carbon dioxide concentrations to plants (both directly and indirectly) [<xref ref-type="bibr" rid="scirp.122967-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.122967-ref4">4</xref>] so that plants can function. In the context of the environment, plants help sequester atmospheric carbon dioxide concentration [<xref ref-type="bibr" rid="scirp.122967-ref5">5</xref>] , thus reducing atmospheric warming potentials.</p><p>Plants have several physiological processes that enable them to function and survive. Some basic physiological processes include photosynthesis, respiration, nutrient and water uptake, and light capture [<xref ref-type="bibr" rid="scirp.122967-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.122967-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.122967-ref8">8</xref>] . To my knowledge, most of these processes have been extensively studied in controlled environments (e.g., in greenhouses). Since atmospheric carbon dioxide concentration is predicted to continue to rise in the future [<xref ref-type="bibr" rid="scirp.122967-ref9">9</xref>] and there are so many plant species around the globe, plants’ sensitivity to changed environmental conditions remains to be understood and elucidated.</p><p>Unlike plant physiology, human physiology consists of a much broader church of systems and is relatively complex. Some examples include blood/air circulation, digestive/excretory, immune, and reproductive and respiratory systems [<xref ref-type="bibr" rid="scirp.122967-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.122967-ref11">11</xref>] . Comparing duration of human physiology with plant physiology is not so straightforward. For example, human physiologists are still trying to understand how the male and the female reproductive system works [<xref ref-type="bibr" rid="scirp.122967-ref11">11</xref>] . Nutrients are one of the critical drivers of photosynthesis [e.g., [<xref ref-type="bibr" rid="scirp.122967-ref12">12</xref>] ], whereas nutrients could have no value to the human body unless they enter the bloodstream. The above examples indicate that there could be data limitations.</p><p>It was in the early 1980s that we came to know that plants can eat air [<xref ref-type="bibr" rid="scirp.122967-ref13">13</xref>] . Subsequently, several earth system models (ESMs) [e.g., [<xref ref-type="bibr" rid="scirp.122967-ref14">14</xref>] [<xref ref-type="bibr" rid="scirp.122967-ref15">15</xref>] ] have been developed to predict terrestrial plants’ carbon, nutrient, and water cycles and scale them up to ecosystem levels. Over the last ten years, much effort has been put into ESMs to improve their carbon, nutrient, and water cycling processes [e.g., [<xref ref-type="bibr" rid="scirp.122967-ref16">16</xref>] ]. One physiological process in plants is related to reproduction, fruiting. Fruiting is rarely represented in ESMs, likely due to a lack of observational data. Therefore, in this study, my main goal is to look into data for some deciduous trees, namely rubber trees from the tropics and explore timings of fruiting.</p></sec><sec id="s2"><title>2. Methods</title><p>It is worth noting that rubber is an agricultural woody crop [<xref ref-type="bibr" rid="scirp.122967-ref17">17</xref>] . Historically rubber trees have been studied for a long time now. Rubber trees start blooming in the spring (around March in the northern hemisphere and July/August in the southern hemisphere) [<xref ref-type="bibr" rid="scirp.122967-ref18">18</xref>] . Rubber trees start producing fruits when they are four years old [<xref ref-type="bibr" rid="scirp.122967-ref19">19</xref>] and after two years following fruiting, the trees become mature [<xref ref-type="bibr" rid="scirp.122967-ref18">18</xref>] .</p><p>To obtain the fruiting data, I looked into studies that I used recently from several geographical locations from Southeast Asiato implement a new rubber plant functional type in a community land model (CLM5) [<xref ref-type="bibr" rid="scirp.122967-ref20">20</xref>] . Since fruiting data was only available in studies from Indonesia [<xref ref-type="bibr" rid="scirp.122967-ref21">21</xref>] and China [<xref ref-type="bibr" rid="scirp.122967-ref22">22</xref>] , I focused on these two studies. I would like to mention that the above two studies are on mature rubber trees.</p></sec><sec id="s3"><title>3. Results &amp; Discussion</title><p>I observed fruiting in rubber trees occurring within eight to nine months from when the rubber tree is dormant. One mechanism could be related to the length of the growing season [<xref ref-type="bibr" rid="scirp.122967-ref18">18</xref>] . Since rubber trees are partly deciduous, I make a generalization that every deciduous tree fruiting takes about eight to nine months since it is dormant (or from the peak dormant time). This is obviously a broad extrapolation or stretch. Nevertheless, I tested this generalization by looking at data from temperate biomes (i.e., sites from Germany) [<xref ref-type="bibr" rid="scirp.122967-ref23">23</xref>] , and the fruiting is around nine to ten months in Germany too. Overall, the duration of this interesting physiological process is analogous to a situation, where women take about nine months to deliver a baby following fertilization. By this comparison, we note that the duration of plant and human physiological processes are similar.</p><p>Rubber trees drop their leaves when fruiting [<xref ref-type="bibr" rid="scirp.122967-ref21">21</xref>] [<xref ref-type="bibr" rid="scirp.122967-ref22">22</xref>] . This means their leaf carbon and transpiration rates decline when they do fruiting. This generally affects rubber trees’ carbon, nutrient, and water cycles. Based on this implication, I recommend that the fruiting process be represented in ESMs for deciduous trees. Data on how fruiting affects leaf carbon and transpiration rates should be collected and looked into from around the globe. ESMs should generally improve their carbon and water biases for deciduous trees.</p><p>Through observation, I think we can find out how interesting nature is! The period of fruiting is similar in deciduous plants and women. This fascinating field needs further study, for example, by collecting more data to see to what extent my argument holds and also question the generalized observation I make. By synthesizing a large dataset, future work can also look into my observation’s coincidence aspect.</p></sec><sec id="s4"><title>4. Conclusion</title><p>My work about fruiting deciduous trees demonstrates how comparisons of duration of plant and human physiology can be made. My findings emphasize that the fruiting process be represented in earth system models for deciduous trees. I also suggest data collection on animal physiological data. Since many animals are so diverse, one can use some advanced techniques available today, such as Machine learning algorithms, and then look into plausible comparisons of duration of animal and plant physiological processes.</p></sec><sec id="s5"><title>Acknowledgements</title><p>I would like to thank Prof. Donald DeAngelis, Dr. Rob Pangle and Dr. Yuanchao Fan for skimming through this manuscript and making suggestions.</p></sec><sec id="s6"><title>Conflicts of Interest</title><p>I have no conflict of interest.</p></sec><sec id="s7"><title>Cite this paper</title><p>Ali, A.A. (2023) Comparing Durations of Plant and Human Physiological Processes and Highlighting Their Importance to the Earth System. American Journal of Plant Sciences, 14, 113-117. https://doi.org/10.4236ajps.2023.142009</p></sec></body><back><ref-list><title>References</title><ref id="scirp.122967-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Kromdijk, J., G&amp;#322;owacka, K., Leonelli, L., et al. (2016) Improving Photosynthesis and Crop Productivity by Accelerating Recovery from Photoprotection. Science, 354, 857-861. https://doi.org/10.1126/science.aai8878</mixed-citation></ref><ref id="scirp.122967-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Keeling, R.F. and Shertz, S.R. (1992) Seasonal and Interannual Variations in Atmospheric Oxygen and Implications for the Global Carbon Cycle. Nature, 358, 723-727. https://doi.org/10.1038/358723a0</mixed-citation></ref><ref id="scirp.122967-ref3"><label>3</label><mixed-citation publication-type="other" xlink:type="simple">Le Quéré, C. andrew, R.M., Canadell, J.G., et al. (2016) Global Carbon Budget 2016. Earth System Science Data, 8, 605-649. https://doi.org/10.5194/essd-8-605-2016</mixed-citation></ref><ref id="scirp.122967-ref4"><label>4</label><mixed-citation publication-type="other" xlink:type="simple">Singh, O.P., Howe, T.A. and Malarvili, M. (2018) Real-Time Human Respiration Carbon Dioxide Measurement Device for Cardiorespiratory Assessment. Journal of Breath Research, 12, Article ID: 026003. https://doi.org/10.1088/1752-7163/aa8dbd</mixed-citation></ref><ref id="scirp.122967-ref5"><label>5</label><mixed-citation publication-type="other" xlink:type="simple">Cernusak, L.A., Haverd, V., Brendel, O., et al. (2019) Robust Response of Terrestrial Plants to Rising CO2. Trends in Plant Science, 24, 578-586.  
https://doi.org/10.1016/j.tplants.2019.04.003</mixed-citation></ref><ref id="scirp.122967-ref6"><label>6</label><mixed-citation publication-type="book" xlink:type="simple">Chapin, F.S. and Eviner, V.T. (2014) 10.6. Biogeochemical Interactions Governing Terrestrial Net Primary Production. In: Holland, H.D. and Turekian, K.K., Eds., Treatise on Geochemistry, 2nd Edition, Elsevier, Oxford, 189-216.  
https://doi.org/10.1016/B978-0-08-095975-7.00806-8</mixed-citation></ref><ref id="scirp.122967-ref7"><label>7</label><mixed-citation publication-type="other" xlink:type="simple">Dyson, B. and Johnson, G. (2014) Photosynthesis: Ecology. eLS.  
https://doi.org/10.1002/9780470015902.a0003198.pub2</mixed-citation></ref><ref id="scirp.122967-ref8"><label>8</label><mixed-citation publication-type="other" xlink:type="simple">McElrone, A.J., Choat, B., Gambetta, G.A. and Brodersen, C.R. (2013) Water Uptake and Transport in Vascular Plants. Nature Education Knowledge, 4, 6.</mixed-citation></ref><ref id="scirp.122967-ref9"><label>9</label><mixed-citation publication-type="other" xlink:type="simple">IPCC (2014) Climate Change 2014: Synthesis Report. Contribution of Working Groups I, II and III to the Fifth Assessment Report of the Intergovernmental Panel on Climate Change. Geneva.</mixed-citation></ref><ref id="scirp.122967-ref10"><label>10</label><mixed-citation publication-type="other" xlink:type="simple">Donina, Z.A. (2011) Intersystem Relationship between Respiration and Blood Circulation. Human Physiology, 37, 229-239.  
https://doi.org/10.1134/S0362119711020034</mixed-citation></ref><ref id="scirp.122967-ref11"><label>11</label><mixed-citation publication-type="other" xlink:type="simple">Ivell, R. and Anand-Ivell, R. (2021) The Physiology of Reproduction—Quo vadis? Frontiers in Physiology, 12, Article ID: 650550.  
https://doi.org/10.3389/fphys.2021.650550</mixed-citation></ref><ref id="scirp.122967-ref12"><label>12</label><mixed-citation publication-type="other" xlink:type="simple">Carstensen, A., Herdean, A., Schmidt, S.B., et al. (2018) The Impacts of Phosphorus Deficiency on the Photosynthetic Electron Transport Chain. Plant Physiology, 177, 271-284. https://doi.org/10.1104/pp.17.01624</mixed-citation></ref><ref id="scirp.122967-ref13"><label>13</label><mixed-citation publication-type="other" xlink:type="simple">Farquhar, G.D., von Caemmerer, S. and Berry, J.A. (1980) A Biochemical Model of Photosynthetic CO2 Assimilation in Leaves of C3 Species. Planta, 149, 78-90.  
https://doi.org/10.1007/BF00386231</mixed-citation></ref><ref id="scirp.122967-ref14"><label>14</label><mixed-citation publication-type="other" xlink:type="simple">Blackmon, M.B. (2001) The Community Climate System Model. Bulletin of the American Meteorological Society, 82, 2357-2376.  
https://doi.org/10.1175/1520-0477(2001)082&lt;2357:TCCSM&gt;2.3.CO;2</mixed-citation></ref><ref id="scirp.122967-ref15"><label>15</label><mixed-citation publication-type="other" xlink:type="simple">Tjiputra, J.F., Roelandt, C., Bentsen, M., et al. (2013) Evaluation of the Carbon Cycle Components in the Norwegian Earth System Model (NorESM). Geoscientific Model Development, 6, 301-325. https://doi.org/10.5194/gmd-6-301-2013</mixed-citation></ref><ref id="scirp.122967-ref16"><label>16</label><mixed-citation publication-type="other" xlink:type="simple">Lawrence, D.M., Fisher, R.A., Koven, C.D., et al. (2019) The Community Land Model Version 5: Description of New Features, Benchmarking, and Impact of Forcing Uncertainty. Journal of Advances in Modeling Earth Systems, 11, 4245-4287.  
https://doi.org/10.1029/2018MS001583</mixed-citation></ref><ref id="scirp.122967-ref17"><label>17</label><mixed-citation publication-type="other" xlink:type="simple">Ziegler, A.D., Fox, J.M. and Xu, J. (2009) The Rubber Juggernaut. Science, 324, 1024-1025. https://doi.org/10.1126/science.1173833</mixed-citation></ref><ref id="scirp.122967-ref18"><label>18</label><mixed-citation publication-type="other" xlink:type="simple">Yeang, H.-Y. (2007) Synchronous Flowering of the Rubber Tree (Hevea brasiliensis) Induced by High Solar Radiation Intensity. New Phytologist, 175, 283-289.  
https://doi.org/10.1111/j.1469-8137.2007.02089.x</mixed-citation></ref><ref id="scirp.122967-ref19"><label>19</label><mixed-citation publication-type="other" xlink:type="simple">Priyadarshan, P.M. (2011) Biology of Hevea Rubber. CAB International, Wallingford. https://doi.org/10.1079/9781845936662.0000</mixed-citation></ref><ref id="scirp.122967-ref20"><label>20</label><mixed-citation publication-type="other" xlink:type="simple">Ali, A.A., Fan, Y., Corre, M.D., et al. (2022) Implementing a New Rubber Plant Functional Type in the Community Land Model (CLM5) Improves Accuracy of Carbon and Water Flux Estimation. Land, 11, 183.  
https://doi.org/10.3390/land11020183</mixed-citation></ref><ref id="scirp.122967-ref21"><label>21</label><mixed-citation publication-type="other" xlink:type="simple">Kotowska, M.M., Leuschner, C., Triadiati, T. and Hertel, D. (2016) Conversion of Tropical Lowland Forest Reduces Nutrient Return through Litterfall, and Alters Nutrient Use Efficiency and Seasonality of Net Primary Production. Oecologia, 180, 601-618. https://doi.org/10.1007/s00442-015-3481-5</mixed-citation></ref><ref id="scirp.122967-ref22"><label>22</label><mixed-citation publication-type="other" xlink:type="simple">Song, Q.-H., Tan, Z.-H., Zhang, Y.-P., et al. (2013) Do the Rubber Plantations in Tropical China Act as Large Carbon Sinks? iForest—Biogeosciences and Forestry, 7, 42-47. https://doi.org/10.3832/ifor0891-007</mixed-citation></ref><ref id="scirp.122967-ref23"><label>23</label><mixed-citation publication-type="other" xlink:type="simple">Mund, M., Herbst, M., Knohl, A., et al. (2020) It Is Not Just a “Trade-Off”: Indications for Sink- and Source-Limitation to Vegetative and Regenerative Growth in an Old-Growth Beech Forest. New Phytologist, 226, 111-125.  
https://doi.org/10.1111/nph.16408</mixed-citation></ref></ref-list></back></article>