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Merge pull request #34 from ckoven/reduced_complexity_docs
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added text on reduced-complexity modes, and update author list
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glemieux authored Jul 10, 2023
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193 changes: 190 additions & 3 deletions docs/source/fates_tech_note.rst
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Expand Up @@ -17,11 +17,12 @@ https://pdfs.semanticscholar.org/396c/b9f172cb681421ed78325a2237bfb428eece.pdf
Authors of FATES code and technical documentation.
^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^

Rosie A. Fisher :sup:`1,2`, Ryan G. Knox :sup:`3`, Charles D. Koven :sup:`3`, Gregory Lemieux :sup:`3`, Chonggang Xu :sup:`4`, Brad Christofferson :sup:`5`, Jacquelyn Shuman :sup:`1`, Maoyi Huang :sup:`6`, Erik Kluzek :sup:`1`, Benjamin Andre :sup:`1`, Jessica F. Needham :sup:`3`, Jennifer Holm :sup:`3`, Marlies Kovenock :sup:`7`, Abigail L. S. Swann :sup:`7`, Stefan Muszala :sup:`1`, Shawn P. Serbin :sup:`8`, Qianyu Li :sup:`8`, Mariana Verteinstein :sup:`1`, Anthony P. Walker :sup:`11`, Alan di Vittorio :sup:`3`, Yilin Fang :sup:`9`, Yi Xu :sup:`6`, Junyan Ding:sup:`12`
Rosie A. Fisher :sup:`1,2`, Ryan G. Knox :sup:`3`, Charles D. Koven :sup:`3`, Gregory Lemieux :sup:`3`, Chonggang Xu :sup:`4`, Brad Christofferson :sup:`5`, Jacquelyn Shuman :sup:`1`, Maoyi Huang :sup:`6`, Erik Kluzek :sup:`1`, Benjamin Andre :sup:`1`, Jessica F. Needham :sup:`3`, Jennifer Holm :sup:`3`, Marlies Kovenock :sup:`7`, Abigail L. S. Swann :sup:`7`, Stefan Muszala :sup:`1`, Shawn P. Serbin :sup:`8`, Qianyu Li :sup:`8`, Mariana Verteinstein :sup:`1`, Anthony P. Walker :sup:`11`, Alan di Vittorio :sup:`3`, Yilin Fang :sup:`9`, Yi Xu :sup:`6`, Junyan Ding :sup:`12`, Shijie Shu :sup:`3`, Marcos Longo :sup:`3`, Adrianna Foster :sup:`1`, Adam Hanbury-Brown :sup:`13`, Lara Kueppers :sup:`13`, Jeffrey Q. Chambers :sup:`13`, Sam Levis :sup:`1`, Zachary Robbins :sup:`4`, Claire Zarakas :sup:`7`


:sup:`1` Climate and Global Dynamics Division, National Center for Atmospheric Research, Boulder, CO, USA

:sup:`2` Centre Européen de Recherche et de Formation Avancée en Calcul Scientifique, Toulouse, France
:sup:`2` Center for International Climate Research (CICERO), Oslo, Norway

:sup:`3` Climate and Ecosystem Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA

Expand All @@ -31,7 +32,7 @@ Rosie A. Fisher :sup:`1,2`, Ryan G. Knox :sup:`3`, Charles D. Koven :sup:`3`, Gr

:sup:`6` Atmospheric Sciences and Global Change Division, Pacific Northwest National Laboratory, Richland, WA, USA

:sup:`7` Department of Biology, University of Washington, Seattle, WA, USA
:sup:`7` University of Washington, Seattle, WA, USA

:sup:`8` Environmental and Climate Sciences Department, Brookhaven National Laboratory, Upton, NY, USA

Expand All @@ -43,6 +44,7 @@ Rosie A. Fisher :sup:`1,2`, Ryan G. Knox :sup:`3`, Charles D. Koven :sup:`3`, Gr

:sup:`12` Earth & Biological Sciences, Pacific Northwest National Laboratory, Richland, WA, USA

:sup:`13` University of California, Berkeley

Introduction
^^^^^^^^^^^^^^^^^^^
Expand Down Expand Up @@ -3856,3 +3858,188 @@ Science*, **8**, 54.

Zeng, Xubin. 2001. “Global Vegetation Root Distribution for Land
Modeling.” *Journal of Hydrometeorology* 2(5): 525–30.




FATES Reduced Complexity Configurations
^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^

The full FATES model has a high degree of structural complexity, with
interactions between processes acting at short timescales such as
photosynthesis and processes acting at longer timescales such as
competition and community restructuring. In order to better isolate
different processes, allow for cleaner experimental design, and
facilitate calibration and testing of different model components,
FATES includes a number of reduced-complexity configurations. A
summary of these configurations is shown in table :ref:`reduced_complexity_table`.

.. _reduced_complexity_table:

.. list-table:: FATES reduced-complexity modes
:widths: 25 25 25 25 25 25
:header-rows: 1
:stub-columns: 0

* - Mode
- How to enable
- Vegetation structure
- Leaf Area Index
- Photosynthesis and Physiology
- Competition between PFTs for canopy space
* - **Primarily site-level modes**
-
-
-
-
-
* - Static Stand Structure (ST3)
- ``use_fates_ed_st3 = .true.``
- Fixed after initialization
- Fixed after initialization
- Active
- No
* - Prescribed Physiology
- ``use_fates_ed_prescribed_phys = .true.``
- Active
- Inactive
- Prescribed NPP per unit crown area and mortality rate
- Active if multiple PFTs present
* - **Primarily large-scale modes**
-
-
-
-
-
* - Satellite Phenology mode (FATES-SP)
- ``use_fates_sp = .true.``
- Simplified: 1 patch per PFT and one cohort per patch
- Prescribed via dynamic dataset
- Active
- No
* - No competition mode, with prescribed biogeography (FATES-nocomp)
- ``use_fates_nocomp = .true., use_fates_fixed_biogeog = .true.``
- Active
- Active
- Active
- No competition: Each PFT allotted a total fixed areas based on
input dataset
* - No competition mode, without prescribed biogeography
- ``use_fates_nocomp = .true., use_fates_fixed_biogeog = .false.``
- Active
- Active
- Active
- No competition: Each PFT allotted the same area everywhere
* - Prescribed biogeography
- ``use_fates_fixed_biogeog = .true.``
- Active
- Active
- Active
- Active, put PFTs only allowed to grow where they are present in
input dataset
* - Full FATES
-
- Active
- Active
- Active
- Active

Each of these modes is described in more detail below. We here
separate them into those that are primarily intended for site-scale
simulations and those that are primarily intended for large-scale
simulations; However we note that all modes have valid use-cases for both
site-scale and large-scale simulations.

Primarily site-level FATES reduced complexity modes
--------------------------------------------------------------------

Two reduced complexity configurations are designed primarily for
site-level testing. These are Static Stand Structure mode and
Prescribed Physiology mode, which enable only the fast-timesale and
slow-timescale processes, respectively.

Static Stand Structure Mode
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
This mode turns of all growth and mortality processes. It is best used
with an inventory initialization to set the initial stand structure as
has been observed at a given location. By turning off growth and
mortality, this mode cuts all feedbacks between fast and slow
processes, and thus can be used to look at changes to physiological
processes or parameters conditional on a given ecosystem structure, or
alternately can be used to calibrate physiological dynamics at a
specific site given known ecosystem structure. Note that leaf
phenology is also disabled in this mode, and thus a user may want to
accomplish similar goals using the Satellite Phenology mode for sites
with strong phenological cycles.

Prescribed Physiology Mode
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
This mode ignores all prognositc physiology calculatino,and instead
allows the user to assert growth and mortality rates in the canopy and
understory. Growth rates are specified via a parameter that governs
the NPP per unit crown area. The crown area scaling is to align
overall growth trajectories as plants grow in size with the full FATES
model: since both light interception and maintenance respiration
(assuming the leaf biomass allometric exponent is the same as that for
crown area) scale with leaf and crown area, this implies an NPP scaling with crown area
as well. Thus this mode allows testign the effects of different ways
of organizing the canopy, or other slow-timescale processes,
conditional on some known growth and mortality rates.

Primarily large-scale FATES reduced complexity modes
--------------------------------------------------------------------

The primarily large-scale reduced complexity modes are designed to
allow separation of processes in support of model complexity
hierarchies and global calibration efforts. A schematic of these
configurations is below:

.. figure:: images/fates_reduced_complexity_modes_slide1.png

Satellite Phenology (FATES-SP) Mode
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
THi sis the simples of the large-scale configurations, and reverts the
behavior of the model as close as possible to the existing CLM-SP and
ELM-SP configurations. In this mode, FATES is given information
about the static areal coverage of each PFT, as well as time-varying
information about LAI and canopy height in the model. FATES uses this
information to construct a canopy structure with a single patch per
PFT and a single cohort per patch, whose stem diameter corresponds
allometrically to the canopy height, and whose number density allows
the cohort to fill the patch given the allometric crown area per
plant. Leaf biomass is dynamically calculated to achieve the
specified LAI for each PFT.

No competition with prescribed biogeography (nocomp) mode
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
In this mode, all processes are active except for light competition
between PFTs. Each PFT is given a total patch area to grow on, but
unlike FATES-SP mode, disturbance can occur on each patch and thus the
space allocated to each PFT may be split into one
or more patches based on disturbance history. Each patch has a PFT
label, and only that PFT is allowed to grow on the patch. Cohorts of
agiven PFT compete against each other for canopy access and thus
light.

No competition without prescribed biogeography mode
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
This mode is imilar to the 'nocomp' mode described above, but instead
of each PFT being allocated areas based on a PFT map read from an
input surface dataset, each PFT is allocated the same area on all
gridcells. Thus it can be used for specific experiemnts looking at PFT
differences across climate gradients.

Prescribed biogeography with competition mode
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
In this mode, PFTs compete against each other, but a given PFT is only
allowed to grow and exist in places where it has some coverage in an
input surface datset. Thus, for example, boreal plants are not
allowed to grow in the tropics and vice-versa, but competition betwen
various plants that coexist in the surface datset can occur. This mode
may also be used to impose biogeographic differences between,
e.g. neotropical versus African and/or Asian tropical forest PFTs.


Full FATES
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
All processes are active.
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