Skip to main content
Powered by ShareScore

Find research datasets worth reusing

Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.

125

datasets available to search

ShareScore release 0.9.0

Reset

Dataset results

125 results for “old growth”

Learn how ShareScore rates datasets ↗
edi60/100

Net Carbon Exchange of an Old-Growth Hemlock Forest at Harvard Forest HEM Tower since 2000

This project estimates carbon exchange rates of multiple forest types at Harvard Forest (see HF072) and compares them to long-term ongoing carbon exchange measurements at the EMS, which is located in a mesic, 60-90 year old red oak and red maple dominated forest on abandoned farmland (HF004). Measurements in each forest type are used to investigate climatic influences on carbon exchange. This mesic hemlock-dominated forest with most trees 100-200 years old on undisturbed soils stored only about 3 Mg/ha of carbon in 2001, compared to over 4 Mg/ha in the 60-90 year old oak/maple stand. However, both sites stored more carbon in 2001 than was measured in the oak/maple stand in any previous year since 1991 (see HF004). The hemlock forest behaved very differently from the oak-maple stand in that the highest rates of carbon storage occurred in spring, while there was very little carbon storage in mid to late summer. Statistical models of carbon exchange in the hemlock forest showed that carbon storage was positively related to daily minimum air temperature in spring, but negatively correlated with soil temperature in the summer. The first effect was attributable to a positive influence of above-freezing minimum temperatures on photosynthesis by hemlock foliage. The negative relationship of soil temperature to carbon storage by hemlock forest in summer was due to exponentially increasing soil and ecosystem respiration, accompanied by a neutral or negative effect of high air temperature on photosynthesis by hemlock trees (see HF063). These effects indicate that carbon storage in the hemlock forest could be strongly affected by climate warming, but the effects will probably be in opposite directions in spring and summer.

openCC0Dec 2023View details →
edi60/100

Dynamics of Old-Growth Forests on Wachusett Mountain in Princeton MA 1996-1997

One of the largest old-growth forests in southern New England was recently "discovered" on the exposed upper slopes of Wachusett Mountain, one of the most heavily used recreational areas in Massachusetts, less than 50 miles from urban Boston. Presettlement and early post-settlement data suggest that most of the area's forests were comprised of a mixture of Quercus rubra and northern hardwood species. Individual species abundances and recruitment dynamics in the four stands exhibit highly variable spatial and temporal patterns across sites that differ in aspect and exposure. Three uneven-aged hardwood stands contain Quercus rubra in the largest size classes, various amounts of Fagus grandifolia, Acer and Betula species in the middle size classes and dense thickets of Acer pennsylvanicum, Acer spicatum, and Hamamelis virginiana in the small size classes. Several individuals of Q. rubra, B. lenta, and B. alleghaniensis are at or very near the maximum longevity known for these species. Of particular significance is the presence of Q. rubra exceeding 250 - 300 years of age. A Tsuga canadensis stand contains unimodal size and age distributions, with trees less than 60-cm dbh and 100 to 300 years old. Widespread Quercus rubra recruitment occurred on all sites from the 1600s through the early 1800s, when it dropped precipitously except for scattered individuals on more open talus sites, and was replaced by either Tsuga or Acer and Betula species. The historical change in recruitment from Quercus to more shade-tolerant species evidently was driven by a change in disturbance regime from an early period when fire was a major factor controlling forest dynamics to a period over the last two centuries when hurricanes (1815 and 1938), frequent wind, ice, and snow damage, but no fire, are documented. The asynchronous nature of tree-ring releases and suppression and the relatively low amount of coarse woody debris corroborate this interpretation. Chronic canopy damage through time p

openCC0Nov 2023View details →
edi56/100

Tree-ring measurements from permanent plot in old-growth hemlock-hardwood forest, Huron Mts., MI

This package includes tree growth-ring widths for increment cores collected from a long-term 'macroplot' established in old-growth hemlock-northern hardwoods forest at the Huron Mts. of northern MI. Tree demographic monitoring data for the entire ca. 3.0 ha macroplot are available in the EDI package edi.1416.1. In 1994 and 1995, increment cores were taken for all 'core-able' trees greater than ~ 10 cm diameter for a subsection of the macroplot about 1 ha in area, along with some additional Tsuga canadensis trees beyond that 1 ha section. Cores are NOT cross-dated. See Methods for more details. This data-package may be cross-referenced to the demographic data in edi.1416.1 using stem numbers.

openCC (other)Dec 2024View details →
edi56/100

Tree-ring measurements from permanent study plot in old-growth hemlock-hardwood forest, Dukes RNA, Hiawatha NF, Marquette Co., MI

This package includes tree growth-ring widths for increment cores collected from a long-term 'macroplot' established in old-growth hemlock-northern hardwoods forest at the Dukes Research Natural Area/Dukes Experimental Forest in the Hiawatha National Forest in Marquette Co., MI. Tree demographic monitoring data for the entire ca. 3.0 ha macroplot, from 1992 to 2019, are available in the EDI package edi.1526.1. In 1993, 1994 and 1995, increment cores were taken for all 'core-able' trees greater than ~ 10 cm diameter for a subsection of the macroplot about 1 ha in area. Trees that were obviously badly rotten and hollow or steeply leaning were not cored. Cores are not cross-dated. See Methods for more details. This data-package may be cross-referenced to the demographic data in edi.1526.1 using stem numbers.

openCC (other)Apr 2025View details →
edi56/100

Towers Forestry Plot, Long-term Vegetation Monitoring in a 1-ha old-growth Rainforest, La Selva Research Station, OTS, Sarapiquí, Heredia, Costa Rica, 2010–2020

The Towers Plot is a 1-hectare permanent vegetation plot established in 2010 under the canopy towers at La Selva Research Station, Sarapiquí, Heredia, Costa Rica. The plot was created by the Organization for Tropical Studies (OTS) to monitor long-term changes in forest structure, composition, and dynamics in an old-growth tropical rainforest. All woody stems with a diameter at breast height (DBH) of 10 cm or greater—including trees, palms, and lianas—were tagged, mapped, and measured following standardized procedures. Censuses were conducted between 2010 and 2020 to document growth, mortality, and recruitment. The dataset includes taxonomic identifications, stem diameter measurements, spatial coordinates within the plot, and metadata describing field methods and species composition. The plot was established beneath three canopy towers that had been previously constructed through the NSF-funded Major Research Instrumentation (MRI) project, NSF 0722741, which provided key infrastructure for canopy and environmental research at La Selva. This proximity created a valuable opportunity to integrate vegetation monitoring with existing environmental instrumentation. Johana Hurtado, coordinator of the Tropical Ecology, Assessment and Monitoring (TEAM) project at La Selva, collaborated with OTS staff in the establishment of the plot, ensuring methodological consistency with other tropical forest monitoring sites. This dataset provides a comprehensive record of woody plant diversity and forest structure in a lowland old-growth Neotropical rainforest. It supports research on forest dynamics, carbon storage, and ecosystem change. The overall monitoring project is ongoing; this data package contains observations from 2010 through 2020.

openCC (other)Oct 2025View details →
edi52/100

Long-term (1935-2019) tree population data from remeasurements of a large network of permanent study plots in old-growth forest, Dukes Research Natural Area, Marquette Co., MI, USA

The Dukes Research Natural Area (Hiawatha National Forest, Marquette Co., MI) amounts to ca. 100 ha of minimally disturbed original forests, including a mix of mesic 'hemlock-northern hardwood' types and peaty wetlands dominated by several species of swamp conifers and black ash (Fraxinus nigra). The RNA hosts a regular grid of 250 0.2-acre (~0.08 ha) permanent monitoring (CFI) plots. This package includes tree censuses for subsets of CFI plots conducted in 1935, 1948, and 1974-1980, and repeated censuses with mapped stems from 1989 to 2019. This 84-year record constitutes one of the longest repeated-measurement, permanent-plot data-sets for old-growth temperate forest.

openCC (other)Dec 2023View details →
edi48/100

Understory plant community data from repeated plot sampling (1978-2019) in old-growth northern hardwood forest, northern Michigan (Dukes RNA, Hiawatha National Forest)

This data-set includes long-term, permanent-plot-based data for understory plant communities in old-growth mixed northern hardwood-hemlock forest and forested peatland in the Upper Great Lakes region. Data for over 900 understory quadrats (all associated with long-term canopy data from larger permanent plots) included multiple (2-5) remeasurements over 23-40 years, with longest periods and most remeasurements for upland forest types. The Dukes Research Natural Area (RNA) (https://www.fs.usda.gov/research/nrs/rnas/locations/dukes) in the Hiawatha National Forest (Marquette Co., MI) includes ca. 100 ha of largely unlogged, original forest. Publications cited below include more detailed information about the site. About half of the RNA supports upland forests intergrading from hemlock (Tsuga candensis) dominance to mixtures of hemlock and northern hardwoods species. Sugar maple (Acer saccharum) is dominant over much of the upland area, with, locally, significant admixtures of beech (Fagus grandifolia), yellow birch (Betula alleghaniensis), and red maple (Acer rubrum). Topographic relief is very slight with total elevational change within the RNA only about 10 m. The stand is within a few km of the western limit of the continuous range of beech. In 1935, 248 continuing forest inventory (CFI) plots (circular, 0.2 acre) were established on a regular grid throughout the RNA, and these have been the subject of repeated sampling through 2018-2019 and support continuing long-term study addressing canopy tree communities (canopy data to be deposited in a separate project). Examples of resulting publications are cited elsewhere in metadata, and can provide more detailed information about the RNA. In 1978-80, U.S. Forest Service researchers, directed by Jan Schultz and Frederick Metzger, initiated studies of understory communities, including herbaceous species and woody seedlings. Data were derived from four sub-quadrats within each of the CFI plots. These quadrats were re-estab

openCC (other)Apr 2023View details →
edi48/100

Long-term (1993-2019) dynamics of tree populations on a mapped 3-ha permanent plot in old-growth northern hardwood forest, Huron Mts., Marquette Co., MI, USA

This data-set includes multiple remeasurements, over 25 years, of all woody stems >2 cm diameter (total of 2125 stems) on a 2.72-ha stem-mapped plot in old-growth northern hardwood forest in the Huron Mountains region of northern Marquette County, MI. The plot and surrounding forest is dominated by sugar maple (Acer saccharum) and eastern hemlock (Tsuga canadensis). Among secondary species, yellow birch (Betula alleghaniensis) and basswood (Tilia americana) are most common. Soils (identified as Kalkaska series) are developed on deep sandy glacial outwash. The plot is within a much larger region of old-growth forest, protected since ca. 1880, with only minimal disturbance associated with access tracks and trails. Numerous other forest community and dendrochronological studies support the interpretation that the area around the study plot has not experienced stand-initiating disturbance for at least 400 years. Initial mapping and measurements (1993-1995 for 2.52 ha; an additional 0.2 ha added in 1999) used a 20x20 m grid established in a near-level area of uniform substrate. All stems were identified to species, mapped on polar coordinates from the center of each grid cell (including, at first measurement, identifiable dead trees, standing and down), and diameter at breast height (dbh) measured to nearest 0.1 cm. All stems were remeasured on a five-year cycle 1999-2019, and new mortality was recorded at each remeasurement. New recruits > 2 cm dbh were added at each remeasurement.

openCC (other)May 2023View details →
edi48/100

Long-term (1962-2019) tree demography on permanent plots in old-growth northern hardwood forests of the Huron Mountains, Marquette Co., Michigan.

This package contains tree demographic data from multiple remeasurements of several sets of permanent study plots in old-growth hemlock-northern hardwood forests in northern Marquette Co., Michigan. Plots were established from 1962-2001, with five to nine censuses over the study period. Plots are distributed over a large and diverse area of old-growth forests protected since ca. 1880, with no commercial management and active management limited to maintenance of trails and tracks. Most plots have not experienced stand-originating disturbances for at least 400 years (based on increment cores); three plots are in stands originating following a fire ca. 1830 ("Bourdo plots" 7094-7096). Forests are dominated by sugar maple (Acer saccharum) and eastern hemlock (Tsuga canadensis); secondary species include yellow birch (Betula alleghaniensis), basswood (Tilia americana), and hop-hornbeam (Ostrya virginiana). Soils are variable, ranging from deep sandy outwash to thin layers of rocky till over bedrock. Mortality and diameter growth of all trees were recorded at each remeasurement. Protocols for measurement and stem-mapping are described in Methods. Several publications use some of the data included in this package -- see 'journal citations'. (identified as Kalkaska series) are developed on deep sandy glacial outwash. The plot is within a much larger region of old-growth forest, protected since ca. 1880, with only minimal disturbance associated with access tracks and trails. Numerous other forest community and dendrochronological studies support the interpretation that the area around the study plot has not experienced stand-initiating disturbance for at least 400 years. Initial mapping and measurements (1993-1995 for 2.52 ha; an additional 0.2 ha added in 1999) used a 20x20 m grid established in a near-level area of uniform substrate. All stems were identified to species, mapped on polar coordinates from the center of each grid cell (including, at first measurement, identif

openCC (other)May 2023View details →
edi48/100

Plot-based vegetation data for a large tract of old--growth hemlock-northern hardwood forest, Marquette Co., Michigan: 1988

In 1987-88 members of the Burton V. Barnes lab at University of Michigan conducted a landscape inventory of portions of the Huron Mountain Club lands (primarily, the self-declared 'Reserved Area') in Powell Township, northern Marquette County, MI. The data-set deposited here, collect under direction of Philip E. Stuart (then a graduate student in the lab) focuses on the ca. 1200 ha of old-growth, mesic hemlock-northern hardwood forests within the larger property. 313 plots (450 m^2) were established at nodes of an approximately 10 chain (~192 m) grid that fell within these forest types. The data-set includes canopy tree measurements, ground-layer cover estimates (for a subpplot), and a number of soil and topographic variables (measured directly and derived). A description of the study and results is published in Simpson et al. 1990. Occasional Papers of the Huron Mountain Wildlife Foundation Number 4, with associated maps.

openCC (other)Jun 2023View details →
edi48/100

Permanent plot data for old-growth white pine - hemlock - hardwood forests in the Huron Mountains, Marquette County, Michigan: 2006-2022

This study was initiated by Dr. Dennis A. Riege with a focus on the role of white pine (Pinus strobus) in old-growth mixed white pine-hemlock-northern hardwood forests. Study areas within the lands of the Huron Mt. Club were selected for prominent presence of canopy white pine. Several permanent study plots, totaling about 3.3 ha, were established, with all trees >5 cm diameter at breast height (dbh) identified, mapped and measured. Initiatl establishment was from 2006-2008. All plots were remeasured in 2011, 2016 and 2021-22. Mortality and new recruits were documented in remeasurements. Reference coordinates for each plot are included in 'Methods'. Data tables in this package include all of these measurements. Additional information, including maps of downed logs, is included in material included under 'other entities'.

openCC (other)Aug 2023View details →
edi48/100

Long-term (1993-2019) tree population measurements from a mapped 2.9-ha permanent plot in old-growth northern hardwood forest, Dukes Research Natural Area, Marquette Co., MI, USA

The Dukes Research Natural Area (Hiawatha National Forest, Marquette Co., MI) amounts to ca. 100 ha of minimally disturbed original forests, including a mix of mesic 'hemlock-northern hardwood' types and peaty wetlands dominated by several species of swamp conifers and black ash (Fraxinus nigra). The RNA hosts a regular grid of 250 permanent monitoring plots (data to be provided in a separate package). In 1993-95, a macroplot of 2.91 ha was established in a mixed mesic upland forest area within the RNA, in which all woody stems >2 cm diameter at breast height (DBH) were identified, measured, and mapped. In 1999 and again every five years subsequently through 2019, the macroplot was recensused; all stems were remeasured, stems newly recruited (>2 cm DBH) were measured and mapped, and any mortality since previous census was noted and described. A severe storm in 2002 resulted in extensive mortality throughout the RNA, particularly in the area in and around the macroplot.

openCC (other)Nov 2023View details →
zenodo44/100

Cellularity & Growth Form: Old Version

<p>Cellularity &amp; growth form data derived from the following sources:&nbsp;</p> <p>Abdullin, S.R., Bagmet, V.B., Nikulin, A.Y., Nikulin, V.Y., Gorpenchenko, T.Y., Grishin, S.Y., Allaguvatova, R.Z. and Gontcharov, A.A., 2022. Emended description of the genus Eremochloris (Trebouxiophyceae, Chlorophyta), with Eremochloris kamchatica sp. nov. from Kamchatka, Russia. Phycologia, 61(2), pp.175-183. <a href="&lt;p>&lt;/p>https://doi.org/10.1080/00318884.2021.2024710"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1080/00318884.2021.2024710">https://doi.org/10.1080/00318884.2021.2024710</a><p></p> <p>Adl, S.M., Bass, D., Lane, C.E., Luke&scaron;, J., Schoch, C.L., Smirnov, A., Agatha, S., Berney, C., Brown, M.W., Burki, F., C&aacute;rdenas, P., Čepička, I., Chistyakova, L., Campo, J. del, Dunthorn, M., Edvardsen, B., Eglit, Y., Guillou, L., Hampl, V., Heiss, A.A., Hoppenrath, M., James, T.Y., Karnkowska, A., Karpov, S., Kim, E., Kolisko, M., Kudryavtsev, A., Lahr, D.J.G., Lara, E., Gall, L.L., Lynn, D.H., Mann, D.G., Massana, R., Mitchell, E.A.D., Morrow, C., Park, J.S., Pawlowski, J.W., Powell, M.J., Richter, D.J., Rueckert, S., Shadwick, L., Shimano, S., Spiegel, F.W., Torruella, G., Youssef, N., Zlatogursky, V., Zhang, Q., 2019. Revisions to the Classification, Nomenclature, and Diversity of Eukaryotes. Journal of Eukaryotic Microbiology 66, 4&ndash;119. <a href="&lt;p>&lt;/p>https://doi.org/10.1111/jeu.12691"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1111/jeu.12691">https://doi.org/10.1111/jeu.12691</a><p></p> <p>Alberghina, J.S., Vigna, M.S., Confalonieri, V.A., 2006. Phylogenetic position of the Oedogoniales within the green algae (Chlorophyta) and the evolution of the absolute orientation of the flagellar apparatus. Plant Syst. Evol. 261, 151&ndash;163. <a href="&lt;p>&lt;/p>https://doi.org/10.1007/s00606-006-0449-2"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1007/s00606-006-0449-2">https://doi.org/10.1007/s00606-006-0449-2</a><p></p> <p>Amaral, R., Fawley, K.P., Němcov&aacute;, Y., &Scaron;evč&iacute;kov&aacute;, T., Luke&scaron;ov&aacute;, A., Fawley, M.W., Santos, L.M. and Eli&aacute;&scaron;, M., 2020. Toward Modern Classification of Eustigmatophytes, Including the Description of Neomonodaceae Fam. Nov. and Three New Genera. Journal of Phycology, 56(3), pp.630-648. <a href="&lt;p>&lt;/p>https://doi.org/10.1111/jpy.12980"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1111/jpy.12980">https://doi.org/10.1111/jpy.12980</a><p></p> <p>Andersen, R.A., 1987. Synurophyceae classis nov., a new class of algae. American journal of botany, 74(3), pp.337-353. <a href="&lt;p>&lt;/p>https://doi.org/10.2307/2443810"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.2307/2443810">https://doi.org/10.2307/2443810</a><p></p> <p>Antonio, M., Schulze-Makuch, D., 2012. Toward a New Understanding of Multicellularity. Hypotheses in the Life Sciences 2, 4&ndash;14. <a href="&lt;p>&lt;/p>http://www.hy-ls.org/index.php/hyls/article/view/89/0"></a></p><p></p><a href="&lt;p>&lt;/p>http://www.hy-ls.org/index.php/hyls/article/view/89/0">http://www.hy-ls.org/index.php/hyls/article/view/89/0</a><p></p> <p>Arneson, R.D., 1973. Pseudotetracystis, a new chlorosarcinean alga. Journal of Phycology, 9(1), pp.10-14. <a href="&lt;p>&lt;/p>https://doi.org/10.1111/j.1529-8817.1973.tb04056.x"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1111/j.1529-8817.1973.tb04056.x">https://doi.org/10.1111/j.1529-8817.1973.tb04056.x</a><p></p> <p>Aslam, Z., Shin, W., Kim, M.K., Im, W.T. and Lee, S.T., 2007. Marinichlorella kaistiae gen. et sp. nov.(Trebouxiophyceae, Chlorophyta) based on polyphasic taxonomy. Journal of Phycology, 43(3), pp.576-584. <a href="&lt;p>&lt;/p>https://doi.org/10.1111/j.1529-8817.2007.00345.x"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1111/j.1529-8817.2007.00345.x">https://doi.org/10.1111/j.1529-8817.2007.00345.x</a><p></p> <p>Badewitz, H. (2004). The genus Microcorycia Cockerell, 1911 (Testacealobosia, Rhizopoda, Protozoa). A critical monograph of the genus including a first description of a new species: Microcorycia scutella n. sp. Lauterbornia 50: 111-146.&nbsp;</p> <p>Bakker, M.E., De Jong, Y.S. and Lokhorst, G.M., 1997. The flagellar apparatus ultrastructure in Leptosira erumpens (Deason &amp; Bold) lukesov&aacute; and its contribution to the understanding of phylogenese relationships within the microthamniales (chlorophyta). Archiv f&uuml;r Protistenkunde, 148(1-2), pp.17-31. <a href="&lt;p>&lt;/p>https://doi.org/10.1016/S0003-9365(97)80033-4"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1016/S0003-9365(97)80033-4">https://doi.org/10.1016/S0003-9365(97)80033-4</a><p></p> <p>Barcytė, D., Hodač, L. and Nedbalov&aacute;, L., 2017. Lunachloris lukesovae gen. et sp. nov.(Trebouxiophyceae, Chlorophyta), a novel coccoid green alga isolated from soil in South Bohemia, Czech Republic. European Journal of Phycology, 52(3), pp.281-291. <a href="&lt;p>&lt;/p>https://doi.org/10.1080/09670262.2017.1283541"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1080/09670262.2017.1283541">https://doi.org/10.1080/09670262.2017.1283541</a><p></p> <p>Barsanti, L., Frassanito, A.M., Passarelli, V., Evangelista, V., Etebari, M., Paccagnini, E., Lupetti, P., Lenzi, P., Verni, F. and Gualtieri, P., 2013. Tetraflagellochloris mauritanica gen. et sp. nov.(Chlorophyceae), a new flagellated alga from the mauritanian desert: morphology, ultrastructure, and phylogenetic framing. Journal of Phycology, 49(1), pp.178-193. <a href="&lt;p>&lt;/p>https://doi.org/10.1111/j.1529-8817.2012.01232.x"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1111/j.1529-8817.2012.01232.x">https://doi.org/10.1111/j.1529-8817.2012.01232.x</a><p></p> <p>Bass, D., Chao, E.E.-Y., Nikolaev, S., Yabuki, A., Ishida, K., Berney, C., Pakzad, U., Wylezich, C., Cavalier-Smith, T., 2009. Phylogeny of Novel Naked Filose and Reticulose Cercozoa: Granofilosea cl. n. and Proteomyxidea Revised. Protist 160, 75&ndash;109. <a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.protis.2008.07.002"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.protis.2008.07.002">https://doi.org/10.1016/j.protis.2008.07.002</a><p></p> <p>Becker, B., Marin, B., 2009. Streptophyte algae and the origin of embryophytes. Annals of Botany 103, 999&ndash;1004. <a href="&lt;p>&lt;/p>https://doi.org/10.1093/aob/mcp044"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1093/aob/mcp044">https://doi.org/10.1093/aob/mcp044</a><p></p> <p>Bernard, Catherine, Alastair G. B. Simpson &amp; David J. Patterson (2000) Some free-living flagellates (protista) from anoxic habitats Ophelia 52(2):113-142. <a href="&lt;p>&lt;/p>https://doi.org/10.1080/00785236.1999.10409422"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1080/00785236.1999.10409422">https://doi.org/10.1080/00785236.1999.10409422</a><p></p> <p>Berney, C., Geisen, S., Van Wichelen, J., Nitsche, F., Vanormelingen, P., Bonkowski, M. and Bass, D., 2015. Expansion of the __reticulosphere__: diversity of novel branching and network-forming amoebae helps to define Variosea (Amoebozoa). Protist, 166(2):271-295. <a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.protis.2015.04.001"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.protis.2015.04.001">https://doi.org/10.1016/j.protis.2015.04.001</a><p></p> <p>Biard, T., 2022. Diversity and ecology of Radiolaria in modern oceans. Environmental Microbiology 24, 2179&ndash;2200. <a href="&lt;p>&lt;/p>https://doi.org/10.1111/1462-2920.16004"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1111/1462-2920.16004">https://doi.org/10.1111/1462-2920.16004</a><p></p> <p>Blackwell, W.H., Letcher, P.M. and Powell, M.J., 2019. Review of Nucleophaga (a primitive,__cryptomycotan__genus): Summary of named and unnamed species, with discussion of contemporary and historical observations. Phytologia, 101, pp.1-18.&nbsp;</p> <p>Bock, C., Luo, W., Kusber, W.H., Hegewald, E., Pažoutov&aacute;, M. and Krienitz, L., 2013. Classification of crucigenoid algae: phylogenetic position of the reinstated genus Lemmermannia, Tetrastrum spp. Crucigenia tetrapedia, and C. lauterbornii (Trebouxiophyceae, Chlorophyta). Journal of Phycology, 49(2), pp.329-339. <a href="&lt;p>&lt;/p>https://doi.org/10.1111/jpy.12039"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1111/jpy.12039">https://doi.org/10.1111/jpy.12039</a><p></p> <p>Bovee, E.C. and Sawyer, T.K., 1979. Marine Flora and Fauna of the Northeastern United States: Protozoa, Sarcodina, Amoebae (Vol. 419). Department of Commerce, National Oceanic and Atmospheric Administration, National Marine Fisheries Service.&nbsp;</p> <p>Bovee, E.C., 1953. Oscillosignum nov. gen. proboscidium nov. sp., type form of its genus, family Mayorellidae, order Amoebida. Transactions of the American Microscopical Society, 72(4):328-332. <a href="&lt;p>&lt;/p>https://doi.org/10.2307/3223477"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.2307/3223477">https://doi.org/10.2307/3223477</a><p></p> <p>Bovee, E.C., 1985. The lobose amebas: III. Descriptions of nine new conopodous amebas of the genus Vexillifera Schaeffek, 1926, emd. Bovee 1951, 1970, with comments on the genus. Archiv f&uuml;r Protistenkunde, 129(1-4):101-118. <a href="&lt;p>&lt;/p>https://doi.org/10.1016/S0003-9365(85)80013-0"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1016/S0003-9365(85)80013-0">https://doi.org/10.1016/S0003-9365(85)80013-0</a><p></p> <p>Brown, M.W., Silberman, J.D. (2013). The Non-dictyostelid Sorocarpic Amoebae. In: Romeralo, M., Baldauf, S., Escalante, R. (eds) Dictyostelids. Springer, Berlin, Heidelberg. <a href="&lt;p>&lt;/p>https://doi.org/10.1007/978-3-642-38487-5_12"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1007/978-3-642-38487-5_12">https://doi.org/10.1007/978-3-642-38487-5_12</a><p></p> <p>Buchheim, M.A., Michalopulos, E.A. and Buchheim, J.A., 2001. Phylogeny of the Chlorophyceae with special reference to the Sphaeropleales: a study of 18S and 26S rDNA data. Journal of Phycology, 37(5), pp.819-835. <a href="&lt;p>&lt;/p>https://doi.org/10.1046/j.1529-8817.2001.00162.x"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1046/j.1529-8817.2001.00162.x">https://doi.org/10.1046/j.1529-8817.2001.00162.x</a><p></p> <p>Burki, F., Roger, A.J., Brown, M.W., Simpson, A.G.B., 2020. The New Tree of Eukaryotes. Trends in Ecology &amp; Evolution 35, 43&ndash;55. <a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.tree.2019.08.008"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.tree.2019.08.008">https://doi.org/10.1016/j.tree.2019.08.008</a><p></p> <p>Bush, M.J., Gallagher, K.A., Chandra, G., Findlay, K.C. and Schlimpert, S., 2022. Hyphal compartmentalization and sporulation in Streptomyces require the conserved cell division protein SepX. Nature Communications, 13(1), pp.1-13. <a href="&lt;p>&lt;/p>https://doi.org/10.1038/s41467-021-27638-1"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1038/s41467-021-27638-1">https://doi.org/10.1038/s41467-021-27638-1</a><p></p> <p>Caisov&aacute;, L., Marin, B., Sausen, N., Pr&ouml;schold, T. and Melkonian, M., 2011. Polyphyly of Chaetophora and Stigeoclonium within the chaetophorales (Chlorophyceae), revealed by sequence comparisons of nuclear-encoded SSU rRNA genes. Journal of Phycology, 47(1), pp.164-177. <a href="&lt;p>&lt;/p>https://doi.org/10.1111/j.1529-8817.2010.00949.x"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1111/j.1529-8817.2010.00949.x">https://doi.org/10.1111/j.1529-8817.2010.00949.x</a><p></p> <p>Carr, M., Leadbeater, B. S., Hassan, R., Nelson, M., &amp; Baldauf, S. L. (2008). Molecular phylogeny of choanoflagellates, the sister group to Metazoa. Proceedings of the National Academy of Sciences of the United States of America, 105(43):16641&ndash;16646. <a href="&lt;p>&lt;/p>https://doi.org/10.1073/pnas.0801667105"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1073/pnas.0801667105">https://doi.org/10.1073/pnas.0801667105</a><p></p> <p>Cavalier-Smith, T., 1998. A revised six-kingdom system of life. Biological Reviews, 73(3), pp.203-266. <a href="&lt;p>&lt;/p>https://doi.org/10.1017/S0006323198005167"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1017/S0006323198005167">https://doi.org/10.1017/S0006323198005167</a><p></p> <p>Cavalier-Smith, T., Chao, E.E.-Y., 2003. Phylogeny and Classification of Phylum Cercozoa (Protozoa). Protist 154, 341&ndash;358. <a href="&lt;p>&lt;/p>https://doi.org/10.1078/143446103322454112"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1078/143446103322454112">https://doi.org/10.1078/143446103322454112</a><p></p> <p>Cavalier-Smith, T., Chao, E.E.-Y., 2006. Phylogeny and megasystematics of phagotrophic heterokonts (kingdom Chromista). J. Mol. Evol. 62, 388&ndash;420. <a href="&lt;p>&lt;/p>https://doi.org/10.1007/s00239-004-0353-8"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1007/s00239-004-0353-8">https://doi.org/10.1007/s00239-004-0353-8</a><p></p> <p>Cavalier-Smith, T., Chao, E.E., Lewis, R., 2016. 187-gene phylogeny of protozoan phylum Amoebozoa reveals a new class (Cutosea) of deep-branching, ultrastructurally unique, enveloped marine Lobosa and clarifies amoeba evolution. Molecular Phylogenetics and Evolution 99, 275&ndash;296. <a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.ympev.2016.03.023"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.ympev.2016.03.023">https://doi.org/10.1016/j.ympev.2016.03.023</a><p></p> <p>Chardez D., Beyens L. (1988). Centropyxis gasparella sp.nov. and Parmulina louisi sp.nov., new testate amoebae from the Canadian High Arctic (Devon Island, NWT). Arch. Protistenkd. 136:337&ndash;344. <a href="&lt;p>&lt;/p>https://doi.org/10.1016/S0003-9365(88)80014-9"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1016/S0003-9365(88)80014-9">https://doi.org/10.1016/S0003-9365(88)80014-9</a><p></p> <p>Cheng, S., Xian, W., Fu, Y., Marin, B., Keller, J., Wu, T., Sun, W., Li, X., Xu, Y., Zhang, Y. and Wittek, S., 2019. Genomes of subaerial Zygnematophyceae provide insights into land plant evolution. Cell, 179(5), pp.1057-1067. <a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.cell.2019.10.019"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.cell.2019.10.019">https://doi.org/10.1016/j.cell.2019.10.019</a><p></p> <p>Chihara, M., Inouye, I. and Takahata, N., 1986. Oltmannsiellopsis, a new genus of marine flagellate (Dunaliellaceae, Chlorophyceae). Archiv f&uuml;r Protistenkunde, 132(4), pp.313-324. <a href="&lt;p>&lt;/p>https://doi.org/10.1016/S0003-9365(86)80026-4"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1016/S0003-9365(86)80026-4">https://doi.org/10.1016/S0003-9365(86)80026-4</a><p></p> <p>Clamp, J.C. and Williams, D., 2006. A Molecular Phylogenetic Investigation of Zoothamnium (Ciliophora, Peritrichia, Sessilida) 1. Journal of Eukaryotic Microbiology, 53(6), pp.494-498. <a href="&lt;p>&lt;/p>https://doi.org/10.1111/j.1550-7408.2006.00132.x"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1111/j.1550-7408.2006.00132.x">https://doi.org/10.1111/j.1550-7408.2006.00132.x</a><p></p> <p>Cocquyt, E., Verbruggen, H., Leliaert, F., De Clerck, O., 2010. Evolution and Cytological Diversification of the Green Seaweeds (Ulvophyceae). Molecular Biology and Evolution 27, 2052&ndash;2061. <a href="&lt;p>&lt;/p>https://doi.org/10.1093/molbev/msq091"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1093/molbev/msq091">https://doi.org/10.1093/molbev/msq091</a><p></p> <p>Coesel, P.F.M., Krienitz, L., 2008. Diversity and geographic distribution of desmids and other coccoid green algae. Biodivers Conserv 17, 381&ndash;392. <a href="&lt;p>&lt;/p>https://doi.org/10.1007/s10531-007-9256-5"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1007/s10531-007-9256-5">https://doi.org/10.1007/s10531-007-9256-5</a><p></p> <p>Cook, M.E., 2004. Structure and asexual reproduction of the enigmatic charophycean green alga Entransia fimbriata (Klebsormidiales, Charophyceae). Journal of Phycology, 40(2), pp.424-431. <a href="&lt;p>&lt;/p>https://doi.org/10.1111/j.1529-8817.2004.03130.x"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1111/j.1529-8817.2004.03130.x">https://doi.org/10.1111/j.1529-8817.2004.03130.x</a><p></p> <p>Cook, M.E., Graham, L.E., 2016. Chlorokybophyceae, Klebsormidiophyceae, Coleochaetophyceae, in: Archibald, J.M., Simpson, A.G.B., Slamovits, C.H., Margulis, L., Melkonian, M., Chapman, D.J., Corliss, J.O. (Eds.), Handbook of the Protists. Springer International Publishing, Cham, pp. 1&ndash;20. <a href="&lt;p>&lt;/p>https://doi.org/10.1007/978-3-319-32669-6_36-1"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1007/978-3-319-32669-6_36-1">https://doi.org/10.1007/978-3-319-32669-6_36-1</a><p></p> <p>Darienko T, Rad-Men&eacute;ndez C, Campbell CN, Pr&ouml;schold T. 2021. Molecular Phylogeny of Unicellular Marine Coccoid Green Algae Revealed New Insights into the Systematics of the Ulvophyceae (Chlorophyta). Microorganisms 9(8):1586. <a href="&lt;p>&lt;/p>https://doi.org/10.3390/microorganisms9081586"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.3390/microorganisms9081586">https://doi.org/10.3390/microorganisms9081586</a><p></p> <p>Darienko, T., Gustavs, L. and Pr&ouml;schold, T., 2016. Species concept and nomenclatural changes within the genera Elliptochloris and Pseudochlorella (Trebouxiophyceae) based on an integrative approach. Journal of Phycology, 52(6), pp.1125-1145. <a href="&lt;p>&lt;/p>https://doi.org/10.1111/jpy.12481"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1111/jpy.12481">https://doi.org/10.1111/jpy.12481</a><p></p> <p>Darienko, T., Gustavs, L., Eggert, A., Wolf, W. and Pr&ouml;schold, T., 2015. Evaluating the species boundaries of green microalgae (Coccomyxa, Trebouxiophyceae, Chlorophyta) using integrative taxonomy and DNA barcoding with further implications for the species identification in environmental samples. PloS one, 10(6), p.e0127838. <a href="&lt;p>&lt;/p>https://doi.org/10.1371/journal.pone.0127838"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1371/journal.pone.0127838">https://doi.org/10.1371/journal.pone.0127838</a><p></p> <p>de Albuquerque, J.P., Keim, C.N. and Lins, U., 2010. Comparative analysis of Beggiatoa from hypersaline and marine environments. Micron, 41(5), pp.507-517. <a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.micron.2010.01.009"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.micron.2010.01.009">https://doi.org/10.1016/j.micron.2010.01.009</a><p></p> <p>Dick, M.W., 2013. Straminipilous Fungi: systematics of the Peronosporomycetes including accounts of the marine straminipilous protists, the plasmodiophorids and similar organisms. Springer Science &amp; Business Media.&nbsp;</p> <p>Dodsworth, J.A., Gevorkian, J., Despujos, F., Cole, J.K., Murugapiran, S.K., Ming, H., Li, W.J., Zhang, G., Dohnalkova, A. and Hedlund, B.P., 2014. Thermoflexus hugenholtzii gen. nov., sp. nov., a thermophilic, microaerophilic, filamentous bacterium representing a novel class in the Chloroflexi, Thermoflexia classis nov., and description of Thermoflexaceae fam. nov. and Thermoflexales ord. nov. International journal of systematic and evolutionary microbiology, 64(Pt_6), pp.2119-2127. <a href="&lt;p>&lt;/p>http://dx.doi.org/10.1099/ijs.0.055855-0"></a></p><p></p><a href="&lt;p>&lt;/p>http://dx.doi.org/10.1099/ijs.0.055855-0">http://dx.doi.org/10.1099/ijs.0.055855-0</a><p></p> <p>Dwyer, J., Burwell, B., Humber, R.A., Mcleod, C., Fleetwood, M., Johnson, T. 2006. Schizangiella serpentis infection in a Virginia ratsnake (Elaphe obsoleta). Veterinary Pathology. 43(5):819-819. Dykov&aacute;, I., Kostka, M. and Peckov&aacute;, H., 2010. Grellamoeba robusta gen. n., sp. n., a possible member of the family Acramoebidae Smirnov, Nassonova et Cavalier-Smith, 2008. European Journal of Protistology, 46(2), pp.77-85. <a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.ejop.2009.10.004"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.ejop.2009.10.004">https://doi.org/10.1016/j.ejop.2009.10.004</a><p></p> <p>Eikrem W. et al. (2017) Haptophyta. In: Archibald J. et al. (eds) Handbook of the Protists. Springer, Cham. <a href="&lt;p>&lt;/p>https://doi.org/10.1007/978-3-319-32669-6_38-2"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1007/978-3-319-32669-6_38-2">https://doi.org/10.1007/978-3-319-32669-6_38-2</a><p></p> <p>Elliott, G.F., 1958. Fossil microproblematica from the Middle East. Micropaleontology, 4(4), pp.419-428. <a href="&lt;p>&lt;/p>https://doi.org/10.2307/1484269"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.2307/1484269">https://doi.org/10.2307/1484269</a><p></p> <p>Figueroa‐Martinez, F., Nedelcu, A.M., Smith, D.R., Reyes‐Prieto, A., 2015. When the lights go out: the evolutionary fate of free‐living colorless green algae. New Phytol 206, 972&ndash;982. <a href="&lt;p>&lt;/p>https://doi.org/10.1111/nph.13279"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1111/nph.13279">https://doi.org/10.1111/nph.13279</a><p></p> <p>Fisher, R.M. and Regenberg, B., 2019. Multicellular group formation in Saccharomyces cerevisiae. Proceedings of the Royal Society B, 286(1910):20191098. <a href="&lt;p>&lt;/p>https://doi.org/10.1098/rspb.2019.1098"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1098/rspb.2019.1098">https://doi.org/10.1098/rspb.2019.1098</a><p></p> <p>Foflonker, F., Mollegard, D., Ong, M., Yoon, H.S. and Bhattacharya, D., 2018. Genomic analysis of Picochlorum species reveals how microalgae may adapt to variable environments. Molecular biology and evolution, 35(11), pp.2702-2711. <a href="&lt;p>&lt;/p>https://doi.org/10.1093/molbev/msy167"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1093/molbev/msy167">https://doi.org/10.1093/molbev/msy167</a><p></p> <p>Freese, J.M. and Lane, C.E., 2017. Parasitism finds many solutions to the same problems in red algae (Florideophyceae, Rhodophyta). Molecular and Biochemical Parasitology, 214, pp.105-111. <a href="&lt;p>&lt;/p>https://10.1016/j.molbiopara.2017.04.006"></a></p><p></p><a href="&lt;p>&lt;/p>https://10.1016/j.molbiopara.2017.04.006">https://10.1016/j.molbiopara.2017.04.006</a><p></p> <p>Friedl, T., 1995. Inferring taxonomic positions and testing genus level assignments in coccoid green lichen algae: a phylogenetic analysis of 18S ribosomal RNA sequences from Dictyochloropsis reticulata and from members of the genus Myrmecia (Chlorophyta, Trebouxiophyceae cl. nov.). Journal of Phycology, 31(4), pp.632-639. <a href="&lt;p>&lt;/p>https://doi.org/10.1111/j.1529-8817.1995.tb02559.x"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1111/j.1529-8817.1995.tb02559.x">https://doi.org/10.1111/j.1529-8817.1995.tb02559.x</a><p></p> <p>Galindo, L.J., Torruella, G., Moreira, D., Eglit, Y., Simpson, A.G., V&ouml;lcker, E., Clau&szlig;, S. and L&oacute;pez-Garc&iacute;a, P., 2019. Combined cultivation and single-cell approaches to the phylogenomics of nucleariid amoebae, close relatives of fungi. Philosophical Transactions of the Royal Society B, 374(1786), p.20190094. <a href="&lt;p>&lt;/p>https://doi.org/10.1098/rstb.2019.0094"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1098/rstb.2019.0094">https://doi.org/10.1098/rstb.2019.0094</a><p></p> <p>Gast, R.J., 2017. Centrohelida and Other Heliozoan-Like Protists, in: Archibald, J.M., Simpson, A.G.B., Slamovits, C.H., Margulis, L., Melkonian, M., Chapman, D.J., Corliss, J.O. (Eds.), Handbook of the Protists. Springer International Publishing, Cham, pp. 1&ndash;17. <a href="&lt;p>&lt;/p>https://doi.org/10.1007/978-3-319-32669-6_28-1"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1007/978-3-319-32669-6_28-1">https://doi.org/10.1007/978-3-319-32669-6_28-1</a><p></p> <p>Gaysina, L., Němcov&aacute;, Y., &Scaron;kaloud, P., &Scaron;evč&iacute;kov&aacute;, T. And Eli&aacute;&scaron;, M., 2013. Chloropyrula uraliensis gen. et sp. nov.(T rebouxiophyceae, Chlorophyta), a new green coccoid alga with a unique ultrastructure, isolated from soil in South Urals. Journal of Systematics and Evolution, 51(4), pp.476-484. <a href="&lt;p>&lt;/p>https://doi.org/10.1111/jse.12014"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1111/jse.12014">https://doi.org/10.1111/jse.12014</a><p></p> <p>Goldstein, S.T. (1999). Foraminifera: A biological overview. In: Modern Foraminifera. Springer, Dordrecht. <a href="&lt;p>&lt;/p>https://doi.org/10.1007/0-306-48104-9_3"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1007/0-306-48104-9_3">https://doi.org/10.1007/0-306-48104-9_3</a><p></p> <p>Gong, S., Li, Z., Zhang, F., Xiao, Y. and Cheng, H., 2018. Symbiochlorum hainanensis gen. et sp. nov.(Ulvophyceae, Chlorophyta) isolated from bleached corals living in the South China Sea. Journal of phycology, 54(6), pp.811-817. <a href="&lt;p>&lt;/p>https://doi.org/10.1111/jpy.12779"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1111/jpy.12779">https://doi.org/10.1111/jpy.12779</a><p></p> <p>Gontcharov, A.A. and Melkonian, M., 2004. Unusual position of the genus Spirotaenia (Zygnematophyceae) among streptophytes revealed by SSU rDNA and rbc L sequence comparisons. Phycologia, 43(1), pp.105-113. <a href="&lt;p>&lt;/p>https://doi.org/10.2216/i0031-8884-43-1-105.1"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.2216/i0031-8884-43-1-105.1">https://doi.org/10.2216/i0031-8884-43-1-105.1</a><p></p> <p>Graf, L., Yang, E.C., Boo, G.H., Andersen, R.A., Yoon, H.S., 2020. Further investigations on the Phaeothamniophyceae using a multigene phylogeny, with descriptions of five new species. Journal of Phycology 56, 358&ndash;379. <a href="&lt;p>&lt;/p>https://doi.org/10.1111/jpy.12950"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1111/jpy.12950">https://doi.org/10.1111/jpy.12950</a><p></p> <p>Grell, K.G. (1966). Am&ouml;ben der Familie Stereomyxidae. Arch.Protistenk. 109, 147-154.&nbsp;</p> <p>Guiry, M.D. in Guiry, M.D. &amp; Guiry, G.M. April 15, 2014. AlgaeBase. World-wide electronic publication, National University of Ireland, Galway. <a href="&lt;p>&lt;/p>https://www.algaebase.org"></a></p><p></p><a href="&lt;p>&lt;/p>https://www.algaebase.org">https://www.algaebase.org</a> <a href="&lt;p>&lt;/p>https://www.algaebase.org/search/genus/detail/?genus_id=45655"><p></p>https://www.algaebase.org/search/genus/detail/?genus_id=45655</a><p></p> <p>Guiry, M.D. in Guiry, M.D. &amp; Guiry, G.M. April 8, 2013. AlgaeBase. World-wide electronic publication, National University of Ireland, Galway. <a href="&lt;p>&lt;/p>https://www.algaebase.org"></a></p><p></p><a href="&lt;p>&lt;/p>https://www.algaebase.org">https://www.algaebase.org</a> <a href="&lt;p>&lt;/p>https://www.algaebase.org/search/genus/detail/?genus_id=43370"><p></p>https://www.algaebase.org/search/genus/detail/?genus_id=43370</a><p></p> <p>Guiry, M.D. in Guiry, M.D. &amp; Guiry, G.M. December 21, 2011. AlgaeBase. World-wide electronic publication, National University of Ireland, Galway. <a href="&lt;p>&lt;/p>https://www.algaebase.org"></a></p><p></p><a href="&lt;p>&lt;/p>https://www.algaebase.org">https://www.algaebase.org</a> <a href="&lt;p>&lt;/p>https://www.algaebase.org/search/genus/detail/?genus_id=46383"><p></p>https://www.algaebase.org/search/genus/detail/?genus_id=46383</a><p></p> <p>Guiry, M.D. in Guiry, M.D. &amp; Guiry, G.M. July 11, 2012. AlgaeBase. World-wide electronic publication, National University of Ireland, Galway. <a href="&lt;p>&lt;/p>https://www.algaebase.org"></a></p><p></p><a href="&lt;p>&lt;/p>https://www.algaebase.org">https://www.algaebase.org</a> <a href="&lt;p>&lt;/p>https://www.algaebase.org/search/genus/detail/?genus_id=43400"><p></p>https://www.algaebase.org/search/genus/detail/?genus_id=43400</a><p></p> <p>Guiry, M.D. in Guiry, M.D. &amp; Guiry, G.M. July 11, 2012. AlgaeBase. World-wide electronic publication, National University of Ireland, Galway. <a href="&lt;p>&lt;/p>https://www.algaebase.org"></a></p><p></p><a href="&lt;p>&lt;/p>https://www.algaebase.org">https://www.algaebase.org</a> <a href="&lt;p>&lt;/p>https://www.algaebase.org/search/genus/detail/?genus_id=43401"><p></p>https://www.algaebase.org/search/genus/detail/?genus_id=43401</a><p></p> <p>Guiry, M.D. in Guiry, M.D. &amp; Guiry, G.M. July 9, 2012. AlgaeBase. World-wide electronic publication, National University of Ireland, Galway. <a href="&lt;p>&lt;/p>https://www.algaebase.org"></a></p><p></p><a href="&lt;p>&lt;/p>https://www.algaebase.org">https://www.algaebase.org</a> <a href="&lt;p>&lt;/p>https://www.algaebase.org/search/genus/detail/?genus_id=43446"><p></p>https://www.algaebase.org/search/genus/detail/?genus_id=43446</a><p></p> <p>Hall J.D., McCourt R. (2017) Zygnematophyta. In: Archibald J. et al. (eds) Handbook of the Protists. Springer, Cham. <a href="&lt;p>&lt;/p>https://doi.org/10.1007/978-3-319-32669-6_41-2"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1007/978-3-319-32669-6_41-2">https://doi.org/10.1007/978-3-319-32669-6_41-2</a><p></p> <p>Hall, J.D. and McCourt, R.M., 2015. Conjugating green algae including desmids. In Freshwater Algae of North America (pp. 429-457). Academic Press. <a href="&lt;p>&lt;/p>https://doi.org/10.1016/B978-0-12-385876-4.00009-8"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1016/B978-0-12-385876-4.00009-8">https://doi.org/10.1016/B978-0-12-385876-4.00009-8</a><p></p> <p>Han, K.Y., Maciszewski, K., Graf, L., Yang, J.H., Andersen, R.A., Karnkowska, A. and Yoon, H.S., 2019. Dictyochophyceae plastid genomes reveal unusual variability in their organization. Journal of phycology, 55(5), pp.1166-1180. <a href="&lt;p>&lt;/p>https://doi.org/10.1111/jpy.12904"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1111/jpy.12904">https://doi.org/10.1111/jpy.12904</a><p></p> <p>Hanada S. (2014) The Phylum Chloroflexi, the Family Chloroflexaceae, and the Related Phototrophic Families Oscillochloridaceae and Roseiflexaceae. In: Rosenberg E., DeLong E.F., Lory S., Stackebrandt E., Thompson F. (eds) The Prokaryotes. Springer, Berlin, Heidelberg. <a href="&lt;p>&lt;/p>https://doi.org/10.1007/978-3-642-38954-2_165"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1007/978-3-642-38954-2_165">https://doi.org/10.1007/978-3-642-38954-2_165</a><p></p> <p>Hassett, B., Vonnahme, T., Peng, X., Jones, E. and Heuz&eacute;, C. (2020) Global diversity and geography of planktonic marine fungi. Botanica Marina, Vol. 63 (Issue 2), pp. 121-139. <a href="&lt;p>&lt;/p>https://doi.org/10.1515/bot-2018-0113"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1515/bot-2018-0113">https://doi.org/10.1515/bot-2018-0113</a><p></p> <p>Heesch, S., Pažoutov&aacute;, M., Moniz, M.B. and Rindi, F., 2016. Prasiolales (Trebouxiophyceae, Chlorophyta) of the Svalbard Archipelago: diversity, biogeography and description of the new genera Prasionella and Prasionema. European Journal of Phycology, 51(2), pp.171-187. <a href="&lt;p>&lt;/p>https://doi.org/10.1080/09670262.2015.1115557"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1080/09670262.2015.1115557">https://doi.org/10.1080/09670262.2015.1115557</a><p></p> <p>Hehenberger, E., Tikhonenkov, D.V., Kolisko, M., Del Campo, J., Esaulov, A.S., Mylnikov, A.P. and Keeling, P.J., 2017. Novel predators reshape holozoan phylogeny and reveal the presence of a two-component signaling system in the ancestor of animals. Current Biology, 27(13), pp.2043-2050. <a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.cub.2017.06.006"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.cub.2017.06.006">https://doi.org/10.1016/j.cub.2017.06.006</a><p></p> <p>Heiss, A.A., Brown, M.W., Simpson, A.G.B., 2016. Apusomonadida, in: Archibald, J.M., Simpson, A.G.B., Slamovits, C.H., Margulis, L., Melkonian, M., Chapman, D.J., Corliss, J.O. (Eds.), Handbook of the Protists. Springer International Publishing, Cham, pp. 1&ndash;27. <a href="&lt;p>&lt;/p>https://doi.org/10.1007/978-3-319-32669-6_15-1"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1007/978-3-319-32669-6_15-1">https://doi.org/10.1007/978-3-319-32669-6_15-1</a><p></p> <p>Herron, M., Nedelcu, A., 2015. Volvocine Algae: From Simple to Complex Multicellularity. pp. 129&ndash;152. <a href="&lt;p>&lt;/p>https://doi.org/10.1007/978-94-017-9642-2_7"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1007/978-94-017-9642-2_7">https://doi.org/10.1007/978-94-017-9642-2_7</a><p></p> <p>Hess, S., 2021. The amoebae of Idionectes vortex (Cutosea, Amoebozoa): Motility, cytoskeleton architecture and extracellular scales. Journal of Eukaryotic Microbiology, 68(6), p.e12869. <a href="&lt;p>&lt;/p>https://doi.org/10.1111/jeu.12869"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1111/jeu.12869">https://doi.org/10.1111/jeu.12869</a><p></p> <p>Heynig, H., 1991. Oocystopsis ng&mdash;eine neue gattung der chlorophyceae (chlorellales, oocystaceae). Archiv f&uuml;r Protistenkunde, 139(1-4), pp.291-294. <a href="&lt;p>&lt;/p>https://doi.org/10.1016/S0003-9365(11)80027-8"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1016/S0003-9365(11)80027-8">https://doi.org/10.1016/S0003-9365(11)80027-8</a><p></p> <p>Hibbett, D.S., Binder, M., Bischoff, J.F., Blackwell, M., Cannon, P.F., Eriksson, O.E., Huhndorf, S., James, T., Kirk, P.M., L&uuml;cking, R., Thorsten Lumbsch, H., Lutzoni, F., Matheny, P.B., McLaughlin, D.J., Powell, M.J., Redhead, S., Schoch, C.L., Spatafora, J.W., Stalpers, J.A., Vilgalys, R., Aime, M.C., Aptroot, A., Bauer, R., Begerow, D., Benny, G.L., Castlebury, L.A., Crous, P.W., Dai, Y.-C., Gams, W., Geiser, D.M., Griffith, G.W., Gueidan, C., Hawksworth, D.L., Hestmark, G., Hosaka, K., Humber, R.A., Hyde, K.D., Ironside, J.E., K&otilde;ljalg, U., Kurtzman, C.P., Larsson, K.-H., Lichtwardt, R., Longcore, J., Miądlikowska, J., Miller, A., Moncalvo, J.-M., Mozley-Standridge, S., Oberwinkler, F., Parmasto, E., Reeb, V., Rogers, J.D., Roux, C., Ryvarden, L., Sampaio, J.P., Sch&uuml;&szlig;ler, A., Sugiyama, J., Thorn, R.G., Tibell, L., Untereiner, W.A., Walker, C., Wang, Z., Weir, A., Weiss, M., White, M.M., Winka, K., Yao, Y.-J., Zhang, N., 2007. A higher-level phylogenetic classification of the Fungi. Mycological Research 111, 509&ndash;547. <a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.mycres.2007.03.004"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.mycres.2007.03.004">https://doi.org/10.1016/j.mycres.2007.03.004</a><p></p> <p>Hindakova, A. and Hindak, F., 1998. Green algae of five city fountains in Bratislava (Slovakia). BIOLOGIA-BRATISLAVA-, 53, pp.481-494. Holland, R.S. and Hergenrader, G.L., 1981. Rhopalosolen saccatus Fott: An Epizoophyte from an Alkaline Lake in Nebraska. American Midland Naturalist, pp.403-405. <a href="&lt;p>&lt;/p>https://doi.org/10.2307/2425179"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.2307/2425179">https://doi.org/10.2307/2425179</a><p></p> <p>Horiguchi T. (2016) Raphidophyceae (Raphidophyta). In: Archibald J. et al. (eds) Handbook of the Protists. Springer, Cham. <a href="&lt;p>&lt;/p>https://doi.org/10.1007/978-3-319-32669-6_37-1"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1007/978-3-319-32669-6_37-1">https://doi.org/10.1007/978-3-319-32669-6_37-1</a><p></p> <p>Horn, S., Ehlers, K., Fritzsch, G., Gil-Rodriguez, M.C., Wilhelm, C. &amp; Schnetter, R. (2007). Synchroma grande spec. nov. (Synchromophyceae class. nov., Heterokontophyta): an ameboid marine alga with unique plastid complexes. Protist 158: 277-293. <a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.protis.2007.02.004"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.protis.2007.02.004">https://doi.org/10.1016/j.protis.2007.02.004</a><p></p> <p>Hudson, P.R. and Waaland, J.R., 1974. Ultrastructure of mitosis and cytokinesis in the multinucleate green alga Acrosiphonia. The Journal of Cell Biology, 62(2), pp.274-294.&nbsp;</p> <p>Irwin, N.A.T., Tikhonenkov, D.V., Hehenberger, E., Mylnikov, A.P., Burki, F., Keeling, P.J., 2019. Phylogenomics supports the monophyly of the Cercozoa. Molecular Phylogenetics and Evolution 130, 416&ndash;423. <a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.ympev.2018.09.004"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.ympev.2018.09.004">https://doi.org/10.1016/j.ympev.2018.09.004</a><p></p> <p>Jahn, T.L., Bovee, E.C. and Griffith, D.L., 1974. Taxonomy and evolution of the Sarcodina: a reclassification. Taxon, 23(4), pp.483-496. </p><p></p>https://doi.org/10.2307/1218771<p></p> <p>Ja&scaron;ke, K., Barcytė, D., P&aacute;nek, T., &Scaron;evč&iacute;kov&aacute;, T., Eli&aacute;&scaron;ov&aacute;, A., Eli&aacute;&scaron;, M., 2022. The net-like heterotrophic amoeba Leukarachnion salinum sp. nov. (Ochrophyta, Stramenopiles) has a cryptic plastid. bioRxiv. <a href="&lt;p>&lt;/p>https://doi.org/10.1101/2022.04.05.487141"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1101/2022.04.05.487141">https://doi.org/10.1101/2022.04.05.487141</a><p></p> <p>John, D.M. and Rindi, F., 2015. Filamentous (nonconjugating) and plantlike green algae. In Freshwater Algae of North America (pp. 375-427). Academic Press. <a href="&lt;p>&lt;/p>https://doi.org/10.1016/B978-0-12-385876-4.00008-6"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1016/B978-0-12-385876-4.00008-6">https://doi.org/10.1016/B978-0-12-385876-4.00008-6</a><p></p> <p>Jones, E.B.G., Suetrong, S., Sakayaroj, J., Bahkali, A.H., Abdel-Wahab, M.A., Boekhout, T., Pang, K.-L., 2015. Classification of marine Ascomycota, Basidiomycota, Blastocladiomycota and Chytridiomycota. Fungal Diversity 73, 1&ndash;72. <a href="&lt;p>&lt;/p>https://doi.org/10.1007/s13225-015-0339-4"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1007/s13225-015-0339-4">https://doi.org/10.1007/s13225-015-0339-4</a><p></p> <p>Jones, M.D., Richards, T.A., Hawksworth, D.L. and Bass, D., 2011. Validation and justification of the phylum name Cryptomycota phyl. nov. IMA fungus, 2(2), pp.173-175. <a href="&lt;p>&lt;/p>https://doi.org/10.5598%2Fimafungus.2011.02.02.08"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.5598%2Fimafungus.2011.02.02.08">https://doi.org/10.5598%2Fimafungus.2011.02.02.08</a><p></p> <p>J&oslash;rgensen, B.B. and Gallardo, V.A., 1999. Thioploca spp.: filamentous sulfur bacteria with nitrate vacuoles. FEMS Microbiology Ecology, 28(4), pp.301-313. <a href="&lt;p>&lt;/p>https://doi.org/10.1111/j.1574-6941.1999.tb00585.x"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1111/j.1574-6941.1999.tb00585.x">https://doi.org/10.1111/j.1574-6941.1999.tb00585.x</a><p></p> <p>Kai, A., Yoshii, Y., Nakayama, T. and Inouye, I., 2008. Aurearenophyceae classis nova, a new class of Heterokontophyta based on a new marine unicellular alga Aurearena cruciata gen. et sp. nov. inhabiting sandy beaches. Protist, 159(3), pp.435-457. <a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.protis.2007.12.003"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.protis.2007.12.003">https://doi.org/10.1016/j.protis.2007.12.003</a><p></p> <p>Karpov, S.A., Mamkaeva, M.A., Aleoshin, V.V., Nassonova, E., Lilje, O. and Gleason, F.H., 2014. Morphology, phylogeny, and ecology of the aphelids (Aphelidea, Opisthokonta) and proposal for the new superphylum Opisthosporidia. Frontiers in Microbiology, 5, p.112. <a href="&lt;p>&lt;/p>https://doi.org/10.3389%2Ffmicb.2014.00112"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.3389%2Ffmicb.2014.00112">https://doi.org/10.3389%2Ffmicb.2014.00112</a><p></p> <p>Katana, A., Kwiatowski, J., Spalik, K., Zakryś, B., Szalacha, E. and Szymańska, H., 2001. Phylogenetic position of Koliella (Chlorophyta) as inferred from nuclear and chloroplast small subunit rDNA. Journal of phycology, 37(3), pp.443-451. <a href="&lt;p>&lt;/p>https://doi.org/10.1046/j.1529-8817.2001.037003443.x"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1046/j.1529-8817.2001.037003443.x">https://doi.org/10.1046/j.1529-8817.2001.037003443.x</a><p></p> <p>Kawachi, M., Inouye, I., Honda, D., O__Kelly, C.J., Bailey, J.C., Bidigare, R.R. and Andersen, R.A., 2002. The Pinguiophyceae classis nova, a new class of photosynthetic stramenopiles whose members produce large amounts of omega‐3 fatty acids. Phycological research, 50(1), pp.31-47. <a href="&lt;p>&lt;/p>https://doi.org/10.1046/j.1440-1835.2002.00260.x"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1046/j.1440-1835.2002.00260.x">https://doi.org/10.1046/j.1440-1835.2002.00260.x</a><p></p> <p>Kawai H., Henry E.C. (2016) Phaeophyta. In: Archibald J. et al. (eds) Handbook of the Protists. Springer, Cham. <a href="&lt;p>&lt;/p>https://doi.org/10.1007/978-3-319-32669-6_31-1"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1007/978-3-319-32669-6_31-1">https://doi.org/10.1007/978-3-319-32669-6_31-1</a><p></p> <p>Kawaichi, S., Ito, N., Kamikawa, R., Sugawara, T., Yoshida, T. and Sako, Y., 2013. Ardenticatena maritima gen. nov., sp. nov., a ferric iron-and nitrate-reducing bacterium of the phylum __Chloroflexi__ isolated from an iron-rich coastal hydrothermal field, and description of Ardenticatenia classis nov. International journal of systematic and evolutionary microbiology, 63(Pt_8), pp.2992-3002. <a href="&lt;p>&lt;/p>https://doi.org/10.1099/ijs.0.046532-0"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1099/ijs.0.046532-0">https://doi.org/10.1099/ijs.0.046532-0</a><p></p> <p>Kim, J.I., Kim, Y.J., Nam, S.W., So, J.E., Hong, S.G., Choi, H.G. and Shin, W., 2020. Taxonomic study of three new Antarctic Asterochloris (Trebouxiophyceae) based on morphological and molecular data. Algae, 35(1), pp.17-32. <a href="&lt;p>&lt;/p>https://doi.org/10.4490/algae.2020.35.2.23"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.4490/algae.2020.35.2.23">https://doi.org/10.4490/algae.2020.35.2.23</a><p></p> <p>Kim, Y.J., 2014. Flora and newly recorded species of three colonial genera (Euteramorus, Coenocystis, and Gloeocystis) in freshwater chlorococcal green algae from Korea. Journal of Ecology and Environment, 37(4), pp.365-378. <a href="&lt;p>&lt;/p>https://doi.org/10.5141/ecoenv.2014.038"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.5141/ecoenv.2014.038">https://doi.org/10.5141/ecoenv.2014.038</a><p></p> <p>Kin, K., Schaap, P., 2021. Evolution of Multicellular Complexity in The Dictyostelid Social Amoebas. Genes 12, 487. <a href="&lt;p>&lt;/p>https://doi.org/10.3390/genes12040487"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.3390/genes12040487">https://doi.org/10.3390/genes12040487</a><p></p> <p>King, N., 2004. The Unicellular Ancestry of Animal Development. Developmental Cell 7, 313&ndash;325. <a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.devcel.2004.08.010"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.devcel.2004.08.010">https://doi.org/10.1016/j.devcel.2004.08.010</a><p></p> <p>Klaveness, D., Br&aring;te, J., Patil, V., Shalchian-Tabrizi, K., Kluge, R., Gisler&oslash;d, H.R. and Jakobsen, K.S., 2011. The 18S and 28S rDNA identity and phylogeny of the common lotic chrysophyte Hydrurus foetidus. European Journal of Phycology, 46(3), pp.282-291. <a href="&lt;p>&lt;/p>https://doi.org/10.1080/09670262.2011.598950"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1080/09670262.2011.598950">https://doi.org/10.1080/09670262.2011.598950</a><p></p> <p>Klimov, V.I. and Zlatogursky, V.V., 2016. Light-and Electron-microscopical Study of Belonocystis marina sp. nov.(Eukaryota: incertae sedis). Protist, 167(5), pp.479-489. <a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.protis.2016.07.003"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.protis.2016.07.003">https://doi.org/10.1016/j.protis.2016.07.003</a><p></p> <p>Kom&aacute;rek, J. and Johansen, J.R., 2015. Filamentous cyanobacteria. In Freshwater Algae of North America (pp. 135-235). Academic Press. <a href="&lt;p>&lt;/p>https://doi.org/10.1016/B978-0-12-385876-4.00004-9"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1016/B978-0-12-385876-4.00004-9">https://doi.org/10.1016/B978-0-12-385876-4.00004-9</a><p></p> <p>Kom&aacute;rek, J., Ka&scaron;tovsk&yacute;, J., Mare&scaron;, J., Johansen, J.R., 2014. Taxonomic classification of cyanoprokaryotes (cyanobacterial genera) 2014, using a polyphasic approach. Preslia 86, 295&ndash;335.&nbsp;</p> <p>Kouwets, F.A. and van der Schaaf, P.J., 1992. Two types of cytoplasmic cleavage in the coenocytic soil alga Protosiphon botryoides (Chlorophyceae). Journal of phycology, 28(4), pp.526-537. <a href="&lt;p>&lt;/p>http://dx.doi.org/10.1111/j.0022-3646.1992.00526.x"></a></p><p></p><a href="&lt;p>&lt;/p>http://dx.doi.org/10.1111/j.0022-3646.1992.00526.x">http://dx.doi.org/10.1111/j.0022-3646.1992.00526.x</a><p></p> <p>Krienitz, L., Bock, C., 2012. Present state of the systematics of planktonic coccoid green algae of inland waters. Hydrobiologia 698:295-326. <a href="&lt;p>&lt;/p>https://doi.org/10.1007/s10750-012-1079-z"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1007/s10750-012-1079-z">https://doi.org/10.1007/s10750-012-1079-z</a><p></p> <p>Kristiansen, J., &Scaron;kaloud, P., 2016. Chrysophyta, in: Archibald, J.M., Simpson, A.G.B., Slamovits, C.H., Margulis, L., Melkonian, M., Chapman, D.J., Corliss, J.O. (Eds.), Handbook of the Protists. Springer International Publishing, Cham, pp. 1&ndash;38. <a href="&lt;p>&lt;/p>https://doi.org/10.1007/978-3-319-32669-6_43-1"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1007/978-3-319-32669-6_43-1">https://doi.org/10.1007/978-3-319-32669-6_43-1</a><p></p> <p>Kuwata, A., Yamada, K., Ichinomiya, M., Yoshikawa, S., Tragin, M., Vaulot, D. and Lopes dos Santos, A., 2018. Bolidophyceae, a sister picoplanktonic group of diatoms&ndash;a review. Frontiers in Marine Science, 5, p.370. <a href="&lt;p>&lt;/p>https://doi.org/10.3389/fmars.2018.00370"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.3389/fmars.2018.00370">https://doi.org/10.3389/fmars.2018.00370</a><p></p> <p>Lax, G., Eglit, Y., Eme, L., Bertrand, E.M., Roger, A.J. and Simpson, A.G., 2018. Hemimastigophora is a novel supra-kingdom-level lineage of eukaryotes. Nature, 564(7736), pp.410-414. <a href="&lt;p>&lt;/p>https://doi.org/10.1038/s41586-018-0708-8"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1038/s41586-018-0708-8">https://doi.org/10.1038/s41586-018-0708-8</a><p></p> <p>Lee, R. E. 2008. Phycology. 4th Edition. Cambridge University Press. Lee, S., Lim, S.R., Jeong, D.G. and Kim, J.H., 2018. Characterization of an oleaginous unicellular green microalga, Lobosphaera incisa (Reisigl, 1964) Strain K-1, isolated from a tidal flat in the Yellow Sea, Republic of Korea. Frontiers in Microbiology, 9, p.2159. <a href="&lt;p>&lt;/p>https://doi.org/10.3389/fmicb.2018.02159"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.3389/fmicb.2018.02159">https://doi.org/10.3389/fmicb.2018.02159</a><p></p> <p>Leliaert, F., Smith, D.R., Moreau, H., Herron, M.D., Verbruggen, H., Delwiche, C.F., De Clerck, O., 2012. Phylogeny and Molecular Evolution of the Green Algae. Critical Reviews in Plant Sciences 31:1&ndash;46. <a href="&lt;p>&lt;/p>https://doi.org/10.1080/07352689.2011.615705"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1080/07352689.2011.615705">https://doi.org/10.1080/07352689.2011.615705</a><p></p> <p>Leliaert, F., Tronholm, A., Lemieux, C., Turmel, M., DePriest, M.S., Bhattacharya, D., Karol, K.G., Fredericq, S., Zechman, F.W. and Lopez-Bautista, J.M., 2016. Chloroplast phylogenomic analyses reveal the deepest-branching lineage of the Chlorophyta, Palmophyllophyceae class. nov. Scientific reports, 6(1), pp.1-13. <a href="&lt;p>&lt;/p>https://doi.org/10.1038/srep25367"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1038/srep25367">https://doi.org/10.1038/srep25367</a><p></p> <p>Lewin RA, Krienitz L, Goericke R, Takeda H, Hepperle D (2000). Picocystis salinarum gen. et sp nov (Chlorophyta) - a new picoplanktonic green alga. Phycologia. 39(6): 560&ndash;565. <a href="&lt;p>&lt;/p>https://doi.org/10.2216/i0031-8884-39-6-560.1"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.2216/i0031-8884-39-6-560.1">https://doi.org/10.2216/i0031-8884-39-6-560.1</a><p></p> <p>Lewis, L.A. and McCourt, R.M., 2004. Green algae and the origin of land plants. American journal of botany, 91(10), pp.1535-1556. <a href="&lt;p>&lt;/p>https://doi.org/10.3732/ajb.91.10.1535"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.3732/ajb.91.10.1535">https://doi.org/10.3732/ajb.91.10.1535</a><p></p> <p>Li, S., Tan, H., Liu, B., Zhu, H., Hu, Z., Liu, G., 2021. Watanabeales ord. nov. and twelve novel species of Trebouxiophyceae (Chlorophyta). Journal of Phycology 57, 1167&ndash;1186. <a href="&lt;p>&lt;/p>https://doi.org/10.1111/jpy.13165"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1111/jpy.13165">https://doi.org/10.1111/jpy.13165</a><p></p> <p>Lindsey, C.R., Rosenzweig, F., Herron, M.D., 2021. Phylotranscriptomics points to multiple independent origins of multicellularity and cellular differentiation in the volvocine algae. BMC Biol 19, 1&ndash;16. <a href="&lt;p>&lt;/p>https://doi.org/10.1186/s12915-021-01087-0"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1186/s12915-021-01087-0">https://doi.org/10.1186/s12915-021-01087-0</a><p></p> <p>Lobban, C.S., Honda, D., Chihara, M. and Schefter, M., 1995. Chrysocystis fragilis gen. nov., sp. nov.(Chrysophyceae, Sarcinochrysidales), with Notes on Other Macroscopic Chrysophytes (Golden Algae) on Guam Reefs. Micronesica, 28(1), pp.91-102.&nbsp;</p> <p>Lokhorst, G.M. and Star, W., 1999. The flagellar apparatus structure in Microspora (Chlorophyceae) confirms a close evolutionary relationship with unicellular green algae. Plant systematics and evolution, 217(1), pp.11-30. <a href="&lt;p>&lt;/p>https://www.jstor.org/stable/23643637"></a></p><p></p><a href="&lt;p>&lt;/p>https://www.jstor.org/stable/23643637">https://www.jstor.org/stable/23643637</a><p></p> <p>Lokhorst, G.M., Star, W. and Zuccarello, G.C., 2004. New genus Koliellopsis (Trebouxiophyceae, Chlorophyta): its phylogenetic position inferred from ultrastructure and nuclear ribosomal DNA sequences. Phycological Research, 52(3), pp.235-243. <a href="&lt;p>&lt;/p>https://doi.org/10.1111/j.1440-183.2004.00350.x"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1111/j.1440-183.2004.00350.x">https://doi.org/10.1111/j.1440-183.2004.00350.x</a><p></p> <p>Lopes dos Santos, A., Pollina, T., Gourvil, P., Corre, E., Marie, D., Garrido, J.L., Rodr&iacute;guez, F., No&euml;l, M.H., Vaulot, D. and Eikrem, W., 2017. Chloropicophyceae, a new class of picophytoplanktonic prasinophytes. Scientific reports, 7(1), pp.1-20. <a href="&lt;p>&lt;/p>https://doi.org/10.1038/s41598-017-12412-5"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1038/s41598-017-12412-5">https://doi.org/10.1038/s41598-017-12412-5</a><p></p> <p>L&oacute;pez-Escard&oacute;, David; L&oacute;pez-Garc&iacute;a, Purificaci&oacute;n; Moreira, David; Ruiz-Trillo, I&ntilde;aki; Torruella, Guifr&eacute; (2017). Parvularia atlantis gen. et sp. nov., a Nucleariid Filose Amoeba (Holomycota, Opisthokonta). Journal of Eukaryotic Microbiology. 65 (2): 170&ndash;179. <a href="&lt;p>&lt;/p>https://doi.org/10.1111%2Fjeu.12450"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1111%2Fjeu.12450">https://doi.org/10.1111%2Fjeu.12450</a><p></p> <p>Lynn, D.H., 2016. Ciliophora, in: Archibald, J.M., Simpson, A.G.B., Slamovits, C.H., Margulis, L., Melkonian, M., Chapman, D.J., Corliss, J.O. (Eds.), Handbook of the Protists. Springer International Publishing, Cham, pp. 1&ndash;52. <a href="&lt;p>&lt;/p>https://doi.org/10.1007/978-3-319-32669-6_23-1"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1007/978-3-319-32669-6_23-1">https://doi.org/10.1007/978-3-319-32669-6_23-1</a><p></p> <p>Lyons, N.A., Kolter, R., 2015. On the evolution of bacterial multicellularity. Current Opinion in Microbiology 24, 21&ndash;28. <a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.mib.2014.12.007"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.mib.2014.12.007">https://doi.org/10.1016/j.mib.2014.12.007</a><p></p> <p>Maistro S., Broady P., Andreoli C., Negrisolo E. (2016) Xanthophyceae. In: Archibald J. et al. (eds) Handbook of the Protists. Springer, Cham. <a href="&lt;p>&lt;/p>https://doi.org/10.1007/978-3-319-32669-6_30-1"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1007/978-3-319-32669-6_30-1">https://doi.org/10.1007/978-3-319-32669-6_30-1</a><p></p> <p>Maistro, S., Broady, P.A., Andreoli, C., Negrisolo, E., 2007. Molecular phylogeny and evolution of the order Tribonematales (Heterokonta, Xanthophyceae) based on analysis of plastidial genes rbcL and psaA. Molecular Phylogenetics and Evolution 43, 407&ndash;417. <a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.ympev.2007.02.014"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.ympev.2007.02.014">https://doi.org/10.1016/j.ympev.2007.02.014</a><p></p> <p>Maistro, S., Broady, P.A., Andreoli, C., Negrisolo, E., 2009. Phylogeny and Taxonomy of Xanthophyceae (Stramenopiles, Chromalveolata). Protist 160, 412&ndash;426. <a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.protis.2009.02.002"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.protis.2009.02.002">https://doi.org/10.1016/j.protis.2009.02.002</a><p></p> <p>Mann D.G., Crawford R.M., Round F.E. (2016) Bacillariophyta. In: Archibald J. et al. (eds) Handbook of the Protists. Springer, Cham. <a href="&lt;p>&lt;/p>https://doi.org/10.1007/978-3-319-32669-6_29-1"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1007/978-3-319-32669-6_29-1">https://doi.org/10.1007/978-3-319-32669-6_29-1</a><p></p> <p>Matthew W Brown, Aaron A Heiss, Ryoma Kamikawa, Yuji Inagaki, Akinori Yabuki, Alexander K Tice, Takashi Shiratori, Ken-Ichiro Ishida, Tetsuo Hashimoto, Alastair G B Simpson, Andrew J Roger. 2018. Phylogenomics Places Orphan Protistan Lineages in a Novel Eukaryotic Super-Group, Genome Biology and Evolution 10(2):427&ndash;433. <a href="&lt;p>&lt;/p>https://doi.org/10.1093/gbe/evy014"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1093/gbe/evy014">https://doi.org/10.1093/gbe/evy014</a><p></p> <p>McCourt, R.M., Karol, K.G., Bell, J., Helm‐Bychowski, K.M., Grajewska, A., Wojciechowski, M.F. and Hoshaw, R.W., 2000. Phylogeny of the conjugating green algae (Zygnemophyceae) based on rbc L sequences. Journal of Phycology, 36(4), pp.747-758. <a href="&lt;p>&lt;/p>https://doi.org/10.1046/j.1529-8817.2000.99106.x"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1046/j.1529-8817.2000.99106.x">https://doi.org/10.1046/j.1529-8817.2000.99106.x</a><p></p> <p>McManus, H.A. and Lewis, L.A., 2005. Molecular phylogenetics, morphological variation and colony-form evolution in the family Hydrodictyaceae (Sphaeropleales, Chlorophyta). Phycologia, 44(6), pp.582-595.&nbsp;</p> <p>McManus, H.A. and Lewis, L.A., 2011. Molecular phylogenetic relationships in the freshwater family Hydrodictyaceae (Sphaeropleales, Chlorophyceae), with an emphasis on Pediastrum duplex. Journal of phycology, 47(1), pp.152-163. <a href="&lt;p>&lt;/p>https://doi.org/10.1111/j.1529-8817.2010.00940.x"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1111/j.1529-8817.2010.00940.x">https://doi.org/10.1111/j.1529-8817.2010.00940.x</a><p></p> <p>Meisterfeld, R. and Badewitz, H., 2006. A redescription of Amphizonella violacea (Amoebozoa: Arcellinida). Acta protozoologica, 45(2), p.167. Mikhailyuk, T., Holzinger, A., Tsarenko, P., Glaser, K., Demchenko, E. and Karsten, U., 2020. Dictyosphaerium‐like morphotype in terrestrial algae: what is Xerochlorella (Trebouxiophyceae, Chlorophyta)?. Journal of phycology, 56(3), pp.671-686. <a href="&lt;p>&lt;/p>https://doi.org/10.1111/jpy.12974"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1111/jpy.12974">https://doi.org/10.1111/jpy.12974</a><p></p> <p>Mikhailyuk, T., Lukesova, A., Glaser, K., Holzinger, A., Obwegeser, S., Nyporko, S., Friedl, T., Karsten, U., 2018. New Taxa of Streptophyte Algae (Streptophyta) from Terrestrial Habitats Revealed Using an Integrative Approach. Protist 169:406-431. </p><p></p>https://doi.org/10.1016/j.protis.2018.03.002<p></p> <p>Mikrjukov, K.A., 1999. Taxonomic revision of scale-bearing heliozoon-like amoebae [Pompholyxophryidae, Rotosphaerida. Acta protozoologica 38(2):119-131.&nbsp;</p> <p>Mu&ntilde;oz-Dorado, J., Marcos-Torres, F.J., Garc&iacute;a-Bravo, E., Moraleda-Mu&ntilde;oz, A., P&eacute;rez, J., 2016. Myxobacteria: Moving, Killing, Feeding, and Surviving Together. Frontiers in Microbiology 7. <a href="&lt;p>&lt;/p>https://doi.org/10.3389/fmicb.2016.00781"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.3389/fmicb.2016.00781">https://doi.org/10.3389/fmicb.2016.00781</a><p></p> <p>Nakada, T. and Nozaki, H., 2015. Flagellate green algae. In Freshwater Algae of North America (pp. 265-313). Academic Press. <a href="&lt;p>&lt;/p>https://doi.org/10.1016/B978-0-12-385876-4.00006-2"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1016/B978-0-12-385876-4.00006-2">https://doi.org/10.1016/B978-0-12-385876-4.00006-2</a><p></p> <p>Nakada, T., Tsuchida, Y., Tomita, M., 2019. Improved taxon sampling and multigene phylogeny of unicellular chlamydomonads closely related to the colonial volvocalean lineage Tetrabaenaceae-Goniaceae-Volvocaceae (Volvocales, Chlorophyceae). Molecular Phylogenetics and Evolution 130, 1&ndash;8. <a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.ympev.2018.09.013"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.ympev.2018.09.013">https://doi.org/10.1016/j.ympev.2018.09.013</a><p></p> <p>Nakayama, T., 2015. Biology, Diversity and Ecology of Free-Living Heterotrophic Flagellates, in: Ohtsuka, S., Suzaki, T., Horiguchi, T., Suzuki, N., Not, F. (Eds.), Marine Protists. Springer Japan, Tokyo, pp. 63&ndash;87. <a href="&lt;p>&lt;/p>https://doi.org/10.1007/978-4-431-55130-0_4"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1007/978-4-431-55130-0_4">https://doi.org/10.1007/978-4-431-55130-0_4</a><p></p> <p>Naranjo-Ortiz, M.A. and Gabald&oacute;n, T., 2019. Fungal evolution: diversity, taxonomy and phylogeny of the Fungi. Biological Reviews, 94(6), pp.2101-2137. <a href="&lt;p>&lt;/p>https://doi.org/10.1111%2Fbrv.12550"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1111%2Fbrv.12550">https://doi.org/10.1111%2Fbrv.12550</a><p></p> <p>Němcov&aacute;, Y., Eli&aacute;&scaron;, M., &Scaron;kaloud, P., Hodač, L. and Neustupa, J., 2011. Jenufa gen. nov.: A new genus of coccoid green algae (chlorophyceae, incertae sedis) previously recorded by environmental sequencing. Journal of Phycology, 47(4), pp.928-938. <a href="&lt;p>&lt;/p>https://doi.org/10.1111/j.1529-8817.2011.01009.x"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1111/j.1529-8817.2011.01009.x">https://doi.org/10.1111/j.1529-8817.2011.01009.x</a><p></p> <p>Neustupa, J., Eli&aacute;&scaron;, M., &Scaron;kaloud, P., Němcov&aacute;, Y. and &Scaron;ejnohov&aacute;, L., 2011. Xylochloris irregularis gen. et sp. nov.(Trebouxiophyceae, Chlorophyta), a novel subaerial coccoid green alga. Phycologia, 50(1), pp.57-66. <a href="&lt;p>&lt;/p>https://doi.org/10.2216/08-64.1"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.2216/08-64.1">https://doi.org/10.2216/08-64.1</a><p></p> <p>Nicholls, K.H. and Wujek, D.E., 2015. Chrysophyceae and Phaeothamniophyceae. In Freshwater Algae of North America (pp. 537-586). Academic Press. <a href="&lt;p>&lt;/p>https://doi.org/10.1016/B978-0-12-385876-4.00012-8"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1016/B978-0-12-385876-4.00012-8">https://doi.org/10.1016/B978-0-12-385876-4.00012-8</a><p></p> <p>Nielsen, Ruth (1987) Marine algae within calcareous shells from New Zealand, New Zealand Journal of Botany, 25(3):425-438. <a href="&lt;p>&lt;/p>https://doi.org/10.1080/0028825X.1987.10413359"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1080/0028825X.1987.10413359">https://doi.org/10.1080/0028825X.1987.10413359</a><p></p> <p>Nishibe, Y., Manage, P.M., Kawabata, Z.I. and Nakano, S.I., 2004. Trophic coupling of a testate amoeba and Microcystis species in a hypertrophic pond. Limnology, 5(2), pp.71-76. <a href="&lt;p>&lt;/p>https://doi.org/10.1007/s10201-004-0114-9"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1007/s10201-004-0114-9">https://doi.org/10.1007/s10201-004-0114-9</a><p></p> <p>O__Kelly, C.J., Wysor, B. and Bellows, W.K., 2004. Gene sequence diversity and the phylogenetic position of algae assigned to the genera Phaeophila and Ochlochaete (Ulvophyceae, Chlorophyta) 1. Journal of Phycology, 40(4), pp.789-799. <a href="&lt;p>&lt;/p>https://doi.org/10.1111/j.1529-8817.2004.03204.x"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1111/j.1529-8817.2004.03204.x">https://doi.org/10.1111/j.1529-8817.2004.03204.x</a><p></p> <p>Olive, L.S. and Stoianovitch, C., 1979. Observations on the mycetozoan genus Ceratiomyxa: description of a new species. Mycologia, 71(3), pp.546-555. <a href="&lt;p>&lt;/p>https://doi.org/10.1080/00275514.1979.12021037"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1080/00275514.1979.12021037">https://doi.org/10.1080/00275514.1979.12021037</a><p></p> <p>Olive, L.S., Bennett, W.E. and Stoianovitch, C., 1983. Redescription of the protostelid genus Microglomus, its type species and a new variety. Transactions of the British Mycological Society, 81(3), pp.449-454. <a href="&lt;p>&lt;/p>https://doi.org/10.1016/S0007-1536(83)80113-2"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1016/S0007-1536(83)80113-2">https://doi.org/10.1016/S0007-1536(83)80113-2</a><p></p> <p>Ott, D.W., Oldham-Ott, C.K., Rybalka, N. and Friedl, T., 2015. Xanthophyte, eustigmatophyte, and raphidophyte algae. In Freshwater Algae of North America (pp. 485-536). Academic Press. <a href="&lt;p>&lt;/p>https://doi.org/10.1016/B978-0-12-385876-4.00011-6"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1016/B978-0-12-385876-4.00011-6">https://doi.org/10.1016/B978-0-12-385876-4.00011-6</a><p></p> <p>Page, F.C., 1975. A new family of amoebae with fine pseudopodia. Zoological Journal of the Linnean Society, 56(1):73-89. <a href="&lt;p>&lt;/p>https://doi.org/10.1111/j.1096-3642.1975.tb00811.x"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1111/j.1096-3642.1975.tb00811.x">https://doi.org/10.1111/j.1096-3642.1975.tb00811.x</a><p></p> <p>Pan, J., Del Campo, J. and Keeling, P.J., 2017. Reference tree and environmental sequence diversity of Labyrinthulomycetes. Journal of Eukaryotic Microbiology, 64(1), pp.88-96. <a href="&lt;p>&lt;/p>https://doi.org/10.1111/jeu.12342"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1111/jeu.12342">https://doi.org/10.1111/jeu.12342</a><p></p> <p>Patterson, D., 1999. The Diversity of Eukaryotes. The American Naturalist 154(supplement):S96-S124. <a href="&lt;p>&lt;/p>https://doi.org/10.2307/2463980"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.2307/2463980">https://doi.org/10.2307/2463980</a><p></p> <p>Patterson, D.J., Simpson, A.G.B. &amp; Rogerson, A. 2000. Amoebae of uncertain affinities. Pages 804-827 in: Lee, J.J., Leedale, G.F. &amp; Bradbury, P., eds. An Illustrated Guide to the Protozoa. 2nd ed., Vol. 2. Society of Protozoologists/Allen Press: Lawrence, Kansas.&nbsp;</p> <p>Pentecost, A. 2021. Tetrasporales. Pages 376-381 in The freshwater algal flora of the British Isles: An identification guide to freshwater and terrestrial algae. Second Edition, John, D.M., Whitton, B.A. and Brook, A.J. eds. Cambridge University Press.&nbsp;</p> <p>Price D.C., Steiner J.M., Yoon H.S., Bhattacharya D., L&ouml;ffelhardt W. (2016) Glaucophyta. In: Archibald J. et al. (eds) Handbook of the Protists. Springer, Cham. <a href="&lt;p>&lt;/p>https://doi.org/10.1007/978-3-319-32669-6_42-1"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1007/978-3-319-32669-6_42-1">https://doi.org/10.1007/978-3-319-32669-6_42-1</a><p></p> <p>Proeschold, T. and Darienko, T., 2020. The green puzzle Stichococcus (Trebouxiophyceae, Chlorophyta): New generic and species concept among this widely distributed genus. Phytotaxa, 441(2), pp.113-142. <a href="&lt;p>&lt;/p>https://doi.org/10.11646/phytotaxa.441.2.2"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.11646/phytotaxa.441.2.2">https://doi.org/10.11646/phytotaxa.441.2.2</a><p></p> <p>Qian, X., Santini, C., Kosta, A., Menguy, N., Guenno, H., Zhang, W., Li, J., Chen, Y., Liu, J., Alberto, F., Espinosa, L., Xiao, T., Wu, L.F., 2019. Juxtaposed membranes underpin cellular adhesion and display unilateral cell division of multicellular magnetotactic prokaryotes. Environmental Microbiology 22(4):1481&ndash;1494. <a href="&lt;p>&lt;/p>https://doi.org/10.1111/1462-2920.14710"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1111/1462-2920.14710">https://doi.org/10.1111/1462-2920.14710</a><p></p> <p>Repetti, S.I., Iha, C., Uthanumallian, K., Jackson, C.J., Chen, Y., Chan, C.X. and Verbruggen, H., 2022. Nuclear genome of a pedinophyte pinpoints genomic innovation and streamlining in the green algae. New Phytologist, 233(5), pp.2144-2154. <a href="&lt;p>&lt;/p>https://doi.org/10.1111/nph.17926"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1111/nph.17926">https://doi.org/10.1111/nph.17926</a><p></p> <p>Rindi, F., 2011. Terrestrial green algae: Systematics, biogeography and expected responses to climate change, in: Climate Change, Ecology and Systematics. pp. 201&ndash;227. <a href="&lt;p>&lt;/p>https://doi.org/10.1017/CBO9780511974540.010"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1017/CBO9780511974540.010">https://doi.org/10.1017/CBO9780511974540.010</a><p></p> <p>Rindi, F., Lopez-Bautista, J.M., Sherwood, A.R. and Guiry, M.D., 2006. Morphology and phylogenetic position of Spongiochrysis hawaiiensis gen. et sp. nov., the first known terrestrial member of the order Cladophorales (Ulvophyceae, Chlorophyta). International Journal of Systematic and Evolutionary Microbiology, 56(4), pp.913-922. <a href="&lt;p>&lt;/p>https://doi.org/10.1099/ijs.0.63977-0"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1099/ijs.0.63977-0">https://doi.org/10.1099/ijs.0.63977-0</a><p></p> <p>Rizvi, S.M., Zhang, C., Freddolino, P.L. and Zhang, Y., 2020. Gut Fungi Possess a Conserved Toxin Immunity Gene of Bacterial Origin. bioRxiv. 2020.10.15.341461 <a href="&lt;p>&lt;/p>https://doi.org/10.1101/2020.10.15.341461"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1101/2020.10.15.341461">https://doi.org/10.1101/2020.10.15.341461</a><p></p> <p>Rosling, A., Cox, F., Cruz-Martinez, K., Ihrmark, K., Grelet, G.A., Lindahl, B.D., Menkis, A. and James, T.Y., 2011. Archaeorhizomycetes: unearthing an ancient class of ubiquitous soil fungi. Science, 333(6044), pp.876-879. <a href="&lt;p>&lt;/p>https://doi.org/10.1126/science.1206958"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1126/science.1206958">https://doi.org/10.1126/science.1206958</a><p></p> <p>Saldarriaga J.F., Taylor F.J.R. (2017) Dinoflagellata. In: Archibald J. et al. (eds) Handbook of the Protists. Springer, Cham. <a href="&lt;p>&lt;/p>https://doi.org/10.1007/978-3-319-32669-6_22-1"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1007/978-3-319-32669-6_22-1">https://doi.org/10.1007/978-3-319-32669-6_22-1</a><p></p> <p>Sawyer, T. K. (1975). Marine amoebae from surface waters of Chincoteague Bay, Virginia: two new genera and nine new species within the families Mayorellidae, Flabellulidae and Stereomyxidae. Transactions of the American Microscopical Society, 94(1):71-92. <a href="&lt;p>&lt;/p>https://doi.org/10.2307/3225533"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.2307/3225533">https://doi.org/10.2307/3225533</a><p></p> <p>Schmidt, M., Horn, S., Ehlers, K., Wilhelm, C. and Schnetter, R., 2015. Guanchochroma wildpretii gen. et spec. nov.(Ochrophyta) Provides New Insights into the Diversification and Evolution of the Algal Class Synchromophyceae. PloS one, 10(7), p.e0131821. <a href="&lt;p>&lt;/p>https://doi.org/10.1371/journal.pone.0131821"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1371/journal.pone.0131821">https://doi.org/10.1371/journal.pone.0131821</a><p></p> <p>Schuler, G.A. and Brown, M.W., 2019. Description of Armaparvus languidus n. gen. n. sp. confirms ultrastructural unity of Cutosea (Amoebozoa, Evosea). Journal of Eukaryotic Microbiology, 66(1), pp.158-166. <a href="&lt;p>&lt;/p>https://doi.org/10.1111/jeu.12640"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1111/jeu.12640">https://doi.org/10.1111/jeu.12640</a><p></p> <p>Sebe-Pedros A, Irimia M, del Campo J, et al (2013) Regulated aggregative multicellularity in a close unicellular relative of metazoa. eLife 2:e01287&ndash;e01287. <a href="&lt;p>&lt;/p>https://doi.org/10.7554/eLife.01287"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.7554/eLife.01287">https://doi.org/10.7554/eLife.01287</a><p></p> <p>Shalchian-Tabrizi, K., Br&aring;te, J., Logares, R., Klaveness, D., Berney, C., Jakobsen, K.S., 2008. Diversification of unicellular eukaryotes: cryptomonad colonizations of marine and fresh waters inferred from revised 18S rRNA phylogeny. Environmental Microbiology 10, 2635&ndash;2644. <a href="&lt;p>&lt;/p>https://doi.org/10.1111/j.1462-2920.2008.01685.x"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1111/j.1462-2920.2008.01685.x">https://doi.org/10.1111/j.1462-2920.2008.01685.x</a><p></p> <p>Shubert, E. and G&auml;rtner, G., 2015. Nonmotile Coccoid and Colonial Green Algae. Freshwater Algae of North America, pp.315-373. <a href="&lt;p>&lt;/p>https://doi.org/10.1016/B978-0-12-385876-4.00007-4"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1016/B978-0-12-385876-4.00007-4">https://doi.org/10.1016/B978-0-12-385876-4.00007-4</a><p></p> <p>Siver, P.A. and Skogstad, A., 2022. A first account of the heterotrophic eukaryote Rabdiophrys Rainer from the fossil record and description of a new species from an ancient Eocene Arctic freshwater lake. European Journal of Protistology, 82, p.125857. <a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.ejop.2021.125857"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.ejop.2021.125857">https://doi.org/10.1016/j.ejop.2021.125857</a><p></p> <p>&Scaron;kaloud, P., Friedl, T., Hallmann, C., Beck, A. and Dal Grande, F., 2016. Taxonomic revision and species delimitation of coccoid green algae currently assigned to the genus Dictyochloropsis (Trebouxiophyceae, Chlorophyta). Journal of Phycology, 52(4), pp.599-617. <a href="&lt;p>&lt;/p>https://doi.org/10.1111/jpy.12422"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1111/jpy.12422">https://doi.org/10.1111/jpy.12422</a><p></p> <p>&Scaron;kaloud, P., Kalina, T., Nemjov&aacute;, K., De Clerck, O. and Leliaert, F., 2013. Morphology and phylogenetic position of the freshwater green microalgae Chlorochytrium (Chlorophyceae) and Scotinosphaera (Scotinosphaerales, ord. nov., Ulvophyceae). Journal of Phycology, 49(1), pp.115-129. <a href="&lt;p>&lt;/p>https://doi.org/10.1111/jpy.12021"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1111/jpy.12021">https://doi.org/10.1111/jpy.12021</a><p></p> <p>&Scaron;kaloud, P., Nedbalov&aacute;, L., Elster, J. and Kom&aacute;rek, J., 2013. A curious occurrence of Hazenia broadyi spec. nova in Antarctica and the review of the genus Hazenia (Ulotrichales, Chlorophyceae). Polar Biology, 36(9), pp.1281-1291. <a href="&lt;p>&lt;/p>https://doi.org/10.1007/s00300-013-1347-z"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1007/s00300-013-1347-z">https://doi.org/10.1007/s00300-013-1347-z</a><p></p> <p>&Scaron;kaloud, P., Rindi, F., Boedeker, C. &amp; Leliaert, F. (2018). S&uuml;&szlig;wasserflora von Mitteleuropa. Freshwater Flora of Central Europe. Bd 13. Chlorophyta: Ulvophyceae (Krienitz, L. ed.). Springer Spektrum, Berlin. <a href="&lt;p>&lt;/p>https://doi.org/10.1007/978-3-662-55495-1_10"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1007/978-3-662-55495-1_10">https://doi.org/10.1007/978-3-662-55495-1_10</a><p></p> <p>Smirnov, A. V., Nassonova, E. S., &amp; Cavalier-Smith, T. (2008). Correct identification of species makes the amoebozoan rRNA tree congruent with morphology for the order Leptomyxida Page 1987; with description of Acramoeba dendroida ng, n. sp., originally misidentified as __Gephyramoeba sp.__. European Journal of Protistology, 44(1):35-44. <a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.ejop.2007.08.001"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.ejop.2007.08.001">https://doi.org/10.1016/j.ejop.2007.08.001</a><p></p> <p>Smirnov, A.V. and Goodkov, A.V., 1999. An illustrated list of basic morphotypes of Gymnamoebia (Rhizopoda, Lobosea). Protistology, 1(1),:20-29. Smirnov, A.V., Chao, E., Nassonova, E.S. and Cavalier-Smith, T., 2011. A revised classification of naked lobose amoebae (Amoebozoa: Lobosa). Protist, 162(4), p.545.&nbsp;</p> <p>Sokulska, M., Kicia, M., Wesołowska, M. and Hendrich, A.B., 2015. Pneumocystis jirovecii&mdash;from a commensal to pathogen: clinical and diagnostic review. Parasitology research, 114(10), pp.3577-3585. <a href="&lt;p>&lt;/p>https://doi.org/10.1007%2Fs00436-015-4678-6"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1007%2Fs00436-015-4678-6">https://doi.org/10.1007%2Fs00436-015-4678-6</a><p></p> <p>Spiegel F.W., Shadwick L.L., Ndiritu G.G., Brown M.W., Aguilar M., Shadwick J.D. (2017) Protosteloid Amoebae (Protosteliida, Protosporangiida, Cavosteliida, Schizoplasmodiida, Fractoviteliida, and Sporocarpic Members of Vannellida, Centramoebida, and Pellitida). In: Archibald J. et al. (eds) Handbook of the Protists. Springer, Cham. <a href="&lt;p>&lt;/p>https://doi.org/10.1007/978-3-319-32669-6_12-1"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1007/978-3-319-32669-6_12-1">https://doi.org/10.1007/978-3-319-32669-6_12-1</a><p></p> <p>&Scaron;tenclov&aacute;, L., Fuč&iacute;kov&aacute;, K., Ka&scaron;tovsk&yacute;, J., Pažoutov&aacute;, M., 2017. Molecular and morphological delimitation and generic classification of the family Oocystaceae (Trebouxiophyceae, Chlorophyta). Journal of Phycology 53, 1263&ndash;1282. <a href="&lt;p>&lt;/p>https://doi.org/10.1111/jpy.12581"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1111/jpy.12581">https://doi.org/10.1111/jpy.12581</a><p></p> <p>Strassert, J.F.H., Wurzbacher, C., Herv&eacute;, V. et al. Long rDNA amplicon sequencing of insect-infecting nephridiophagids reveals their affiliation to the Chytridiomycota and a potential to switch between hosts. Sci Rep 11, 396 (2021). <a href="&lt;p>&lt;/p>https://doi.org/10.1038/s41598-020-79842-6"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1038/s41598-020-79842-6">https://doi.org/10.1038/s41598-020-79842-6</a><p></p> <p>Sugimoto, H. and Endoh, H., 2006. Analysis of fruiting body development in the aggregative ciliate Sorogena stoianovitchae (Ciliophora, Colpodea). Journal of Eukaryotic Microbiology, 53(2), pp.96-102. <a href="&lt;p>&lt;/p>https://doi.org/10.1111/j.1550-7408.2005.00077.x"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1111/j.1550-7408.2005.00077.x">https://doi.org/10.1111/j.1550-7408.2005.00077.x</a><p></p> <p>Temraleeva, A., Moskalenko, S., Mincheva, E., Bukin, Y. and Sinetova, M., 2018. Spongiosarcinopsis terrestris gen. et sp. nov.(Chlorophyta, Chlorophyceae): a new genus of green algae from gray forest soil, Russia. Phytotaxa, 376(6), pp.291-300. <a href="&lt;p>&lt;/p>http://dx.doi.org/10.11646/phytotaxa.376.6.4"></a></p><p></p><a href="&lt;p>&lt;/p>http://dx.doi.org/10.11646/phytotaxa.376.6.4">http://dx.doi.org/10.11646/phytotaxa.376.6.4</a><p></p> <p>Tennant, R.K., Lux, T.M., Sambles, C.M., Kuhn, N.J., Petticrew, E.L., Oldfield, R., Parker, D.A., Hatton, J., Moore, K.A., Lee, R. and Turney, C.S., 2019. Palaeogenomics of the hydrocarbon producing microalga Botryococcus braunii. Scientific reports, 9(1), pp.1-10. <a href="&lt;p>&lt;/p>https://doi.org/10.1038/s41598-018-38236-5"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1038/s41598-018-38236-5">https://doi.org/10.1038/s41598-018-38236-5</a><p></p> <p>Thompson, R.H., 1952. A new genus and new records of algae in the Chlorococcales. American journal of botany, pp.365-367. <a href="&lt;p>&lt;/p>https://doi.org/10.2307/2438780"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.2307/2438780">https://doi.org/10.2307/2438780</a><p></p> <p>Toome, M., Roberson, R.W., Aime, M.C., 2013. Meredithblackwellia eburnea gen. et sp. nov., Kriegeriaceae fam. nov. and Kriegeriales ord. nov.&mdash;toward resolving higher-level classification in Microbotryomycetes. Mycologia 105, 486&ndash;495. <a href="&lt;p>&lt;/p>https://doi.org/10.3852/12-251"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.3852/12-251">https://doi.org/10.3852/12-251</a><p></p> <p>Tragin, M., Vaulot, D. Novel diversity within marine Mamiellophyceae (Chlorophyta) unveiled by metabarcoding. Sci Rep 9, 5190 (2019). <a href="&lt;p>&lt;/p>https://doi.org/10.1038/s41598-019-41680-6"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1038/s41598-019-41680-6">https://doi.org/10.1038/s41598-019-41680-6</a><p></p> <p>Trainor, F.R. and McLean, R.J., 1964. A study of a new species of Spongiochloris introduced into sterile soil. American Journal of Botany, 51(1), pp.57-60. <a href="&lt;p>&lt;/p>https://doi.org/10.2307/2440064"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.2307/2440064">https://doi.org/10.2307/2440064</a><p></p> <p>Trojan, D., Schreiber, L., Bjerg, J.T., B&oslash;ggild, A., Yang, T., Kjeldsen, K.U. and Schramm, A., 2016. A taxonomic framework for cable bacteria and proposal of the candidate genera Electrothrix and Electronema. Systematic and applied microbiology, 39(5), pp.297-306. <a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.syapm.2016.05.006"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.syapm.2016.05.006">https://doi.org/10.1016/j.syapm.2016.05.006</a><p></p> <p>Ulrich, S. and R&ouml;ske, K., 2018. Autumnella lusatica gen. nov. and sp. nov.(Chlorophyta, Trebouxiophyceae), a new phytoplankton species in acidic lignite pit lakes. Phycologia, 57(3), pp.251-261. <a href="&lt;p>&lt;/p>https://doi.org/10.2216/17-46.1"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.2216/17-46.1">https://doi.org/10.2216/17-46.1</a><p></p> <p>Umen J. G. (2014). Green algae and the origins of multicellularity in the plant kingdom. Cold Spring Harbor perspectives in biology, 6(11), a016170. <a href="&lt;p>&lt;/p>https://doi.org/10.1101/cshperspect.a016170"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1101/cshperspect.a016170">https://doi.org/10.1101/cshperspect.a016170</a><p></p> <p>Ustinova I, Krienitz L, Huss VAR. 2000. Hyaloraphidium curvatum is not a green alga, but a lower fungus; Amobedium parasiticum is not a fungus, but a member of the DRIPs. Protist 151:253&ndash;262. <a href="&lt;p>&lt;/p>https://doi.org/10.1078/1434-4610-00023"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1078/1434-4610-00023">https://doi.org/10.1078/1434-4610-00023</a><p></p> <p>Van Wichelen, J., D__hondt, S., Claeys, M., Vyverman, W., Berney, C., Bass, D. and Vanormelingen, P., 2016. A hotspot of amoebae diversity: 8 new naked amoebae associated with the planktonic bloom-forming cyanobacterium Microcystis. Acta Protozoologica, 55(2):61-87. <a href="&lt;p>&lt;/p>https://doi.org/10.4467/16890027AP.16.007.4942"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.4467/16890027AP.16.007.4942">https://doi.org/10.4467/16890027AP.16.007.4942</a><p></p> <p>Vančurov&aacute;, L., Peksa, O., Němcov&aacute;, Y. and &Scaron;kaloud, P., 2015. Vulcanochloris (Trebouxiales, Trebouxiophyceae), a new genus of lichen photobiont from La Palma, Canary Islands, Spain. Phytotaxa, 219(2), pp.118-132. <a href="&lt;p>&lt;/p>http://dx.doi.org/10.11646/phytotaxa.219.2.2"></a></p><p></p><a href="&lt;p>&lt;/p>http://dx.doi.org/10.11646/phytotaxa.219.2.2">http://dx.doi.org/10.11646/phytotaxa.219.2.2</a><p></p> <p>Vavra, J. and Kucera, K., 1970. Pneumocystis carinii Delanoe, its ultrastructure and ultrastructural affinities. The Journal of protozoology, 17(3), pp.463-483. <a href="&lt;p>&lt;/p>https://doi.org/10.2307/2463980"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.2307/2463980">https://doi.org/10.2307/2463980</a><p></p> <p>Vega, F.E. and Kaya, H.K., 2012. Insect pathology. Academic press. Verbruggen, H., Ashworth, M., LoDuca, S.T., Vlaeminck, C., Cocquyt, E., Sauvage, T., Zechman, F.W., Littler, D.S., Littler, M.M., Leliaert, F. and De Clerck, O., 2009. A multi-locus time-calibrated phylogeny of the siphonous green algae. Molecular phylogenetics and evolution, 50(3), pp.642-653. <a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.ympev.2008.12.018"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1016/j.ympev.2008.12.018">https://doi.org/10.1016/j.ympev.2008.12.018</a><p></p> <p>Visnovsky, G. &amp; P. M. Novis, 2012. Novel alpine algae from New Zealand: Chlorophyta. Phytotaxa 39, 1-30. <a href="&lt;p>&lt;/p>https://doi.org/10.11646/phytotaxa.39.1.1"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.11646/phytotaxa.39.1.1">https://doi.org/10.11646/phytotaxa.39.1.1</a><p></p> <p>Walker, G., Dorrell, R., Schlacht, A., Dacks, J., 2011. Eukaryotic systematics: A user__s guide for cell biologists and parasitologists. Parasitology 138, 1638&ndash;63. <a href="&lt;p>&lt;/p>https://doi.org/10.1017/S0031182010001708"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1017/S0031182010001708">https://doi.org/10.1017/S0031182010001708</a><p></p> <p>Watanabe, S. and Lewis, L.A., 2017. Phylogenetic interpretation of light and electron microscopic features of selected members of the phylogroup Moewusinia (Chlorophyceae), with new generic taxonomy. Phycologia, 56(3), pp.329-353. <a href="&lt;p>&lt;/p>https://doi.org/10.2216/16-64.1"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.2216/16-64.1">https://doi.org/10.2216/16-64.1</a><p></p> <p>Watanabe, S. and Nakayama, T., 2007. Ultrastructure and phylogenetic relationships of the unicellular green algae Ignatius tetrasporus and Pseudocharacium americanum (Chlorophyta). Phycological Research, 55(1), pp.1-16. <a href="&lt;p>&lt;/p>https://doi.org/10.1111/j.1440-1835.2006.00439.x"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1111/j.1440-1835.2006.00439.x">https://doi.org/10.1111/j.1440-1835.2006.00439.x</a><p></p> <p>Watanabe, S., 1981. Observations on Urnella terrestris PLAYFAIR (Chlorophyceae, Chlorococcales) in culture. Phycologia, 20(1), pp.12-15. <a href="&lt;p>&lt;/p>https://doi.org/10.2216/i0031-8884-20-1-12.1"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.2216/i0031-8884-20-1-12.1">https://doi.org/10.2216/i0031-8884-20-1-12.1</a><p></p> <p>Watanabe, S., Fuč&iacute;kov&aacute;, K., Lewis, L.A. and Lewis, P.O., 2016. Hiding in plain sight: Koshicola spirodelophila gen. et sp. nov.(Chaetopeltidales, Chlorophyceae), a novel green alga associated with the aquatic angiosperm Spirodela polyrhiza. American Journal of Botany, 103(5), pp.865-875. <a href="&lt;p>&lt;/p>https://doi.org/10.3732/ajb.1500481"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.3732/ajb.1500481">https://doi.org/10.3732/ajb.1500481</a><p></p> <p>Watanabe, S., Mitui, K., Nakayama, T. and Inouye, I., 2002. Phylogenetic analyses of the species of Chlorosarcinopsis and Neochlorosarcina (Chlorophyceae). Journal of Phycology, 38, pp.36-36. <a href="&lt;p>&lt;/p>https://doi.org/10.1046/j.1529-8817.38.s1.103.x"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1046/j.1529-8817.38.s1.103.x">https://doi.org/10.1046/j.1529-8817.38.s1.103.x</a><p></p> <p>Wetherbee, R. and Verbruggen, H., 2016. Kraftionema allantoideum, a new genus and family of Ulotrichales (Chlorophyta) adapted for survival in high intertidal pools. Journal of Phycology, 52(5), pp.704-715. <a href="&lt;p>&lt;/p>https://doi.org/10.1111/jpy.12447"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1111/jpy.12447">https://doi.org/10.1111/jpy.12447</a><p></p> <p>Wetherbee, R., Bringloe, T.T., Costa, J.F., van de Meene, A., Andersen, R.A. and Verbruggen, H., 2021. New pelagophytes show a novel mode of algal colony development and reveal a perforated theca that may define the class. Journal of Phycology, 57(2), pp.396-411. <a href="&lt;p>&lt;/p>https://doi.org/10.1111/jpy.13074-20-137"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1111/jpy.13074-20-137">https://doi.org/10.1111/jpy.13074-20-137</a><p></p> <p>Wetherbee, R., Jackson, C.J., Repetti, S.I., Clementson, L.A., Costa, J.F., van de Meene, A., Crawford, S. and Verbruggen, H., 2019. The golden paradox&ndash;a new heterokont lineage with chloroplasts surrounded by two membranes. Journal of phycology, 55(2), pp.257-278. <a href="&lt;p>&lt;/p>https://doi.org/10.1111/jpy.12822"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1111/jpy.12822">https://doi.org/10.1111/jpy.12822</a><p></p> <p>Wolf, M., Buchheim, M., Hegewald, E., Krienitz, L. and Hepperle, D., 2002. Phylogenetic position of the Sphaeropleaceae (Chlorophyta). Plant Systematics and Evolution, 230(3), pp.161-171. <a href="&lt;p>&lt;/p>https://doi.org/10.1007/s006060200002"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1007/s006060200002">https://doi.org/10.1007/s006060200002</a><p></p> <p>Wujek, D.E. The first occurrence of the coccoid green alga Borodinella polytetras. Miller in North America (Michigan). Great Lakes Bot. 59(3-4):94-98. <a href="&lt;p>&lt;/p>http://hdl.handle.net/2027/spo.0497763.0058.107"></a></p><p></p><a href="&lt;p>&lt;/p>http://hdl.handle.net/2027/spo.0497763.0058.107">http://hdl.handle.net/2027/spo.0497763.0058.107</a><p></p> <p>Wujek, D.E., 2016. The chlorococcalean Green Alga Hydrianum Rabenhorst from North America (Kansas and Michigan). Transactions of the Kansas Academy of Science, 119(1), pp.105-108. <a href="&lt;p>&lt;/p>https://www.jstor.org/stable/24887848"></a></p><p></p><a href="&lt;p>&lt;/p>https://www.jstor.org/stable/24887848">https://www.jstor.org/stable/24887848</a><p></p> <p>Yoon H.S. et al. (2016) Rhodophyta. In: Archibald J. et al. (eds) Handbook of the Protists. Springer, Cham. <a href="&lt;p>&lt;/p>https://doi.org/10.1007/978-3-319-32669-6_33-1"></a></p><p></p><a href="&lt;p>&lt;/p>https://doi.org/10.1007/978-3-319-32669-6_33-1">https://doi.org/10.1007/978-3-319-32669-6_33-1</a><p></p><p></p>

opencc-zeroAug 2024View details →
edi44/100

Fire history dendrochronology study, super old growth data, central western Cascades, Oregon, 2002 (Giglia thesis)

The primary objectives of this study were to assay where super old-growth (SOG) persists on the landscape, what factors enabled it to survive for more than 550 years, and to develop a predictive model for the occurrence of SOG. To meet these objectives, data were synthesized from prior fire history work done in the central western Cascades of Oregon (Morrison and Swanson unpublished; Teensma 1987; Morrison and Swanson 1990; Weisberg 1998). The study involved the following steps: (1) the collection of primary data and maps from each study, (2) the creation of a master database, and (3) analysis of the synthesized data.

openCustomDec 2013View details →
edi44/100

Soil respiration associated with ectomycorrhizal mats in an old-growth stand along lower Lookout Creek, HJ Andrews Experimental Forest (2008-2009)

Comparisons of respiration rate and environmental variables for mat and non-mat soil were conducted between July 2008 to Nov 2009 in a 0.1ha plot adjacent lower Lookout Creek, approximately 700m downstream from Lookout Camp (44 deg 13”25’N, 122 deg 15”30’W, 484m above sea level). The predominant overstory species are Psuedotsuga menziesii, Tsuga heterophylla, and Thuja Plicata. Associated ectomycorrhizal communities were measured over the 1.5 year period and data collection for the study is complete. Soil respiration was measured using LiCOR instrumentation, and analyses were performed computationally by correlating soil respiration with known environmental metrics (moisture, temperature, etc.) measured in other studies (TW006, MV001, etc.).

openCustomAug 2013View details →
edi44/100

Stand Dynamics and Radial Growth Measurements from Old-Growth and Secondary-Growth Forests at the Coweeta Hydrologic Laboratory and Joyce Kilmer Wilderness Area

Our objectives were to define disturbance causes, rates (percent disturbance per decade), magnitudes and frequency (time since last disturbance) for both secondary and old-growth mixed-oak stands, and to determine if all mixed oak stands experience similar disturbance history.

openCustomJan 2020View details →
zenodo40/100

Meteorological and Ecosystem Flux Data for: Net ecosystem production in an old-growth tropical dry forest in Northwestern Mexico

<p>This dataset accompanies the paper: Net ecosystem production in an old-growth tropical dry forest in Northwestern M&eacute;xico which is submitted for publication at the Journal of Geophysical Research - Biogeosciences</p> <p>With this data set, we explore the functionality as a carbon source or sink&nbsp;of an old-growth tropical dry forest&nbsp;in the carbon cycle and its functional relationship&nbsp;with&nbsp;water and light across years with different precipitation patterns in Northwestern&nbsp;M&eacute;xico, using 3&nbsp;continuous years of water, energy, and carbon flux measurements from an eddy covariance tower and also a meteorological arrangement.</p>

opencc-by-4.0Dec 2019View details →
zenodo40/100

LiDAR-derived forest structure data and predictions of the locations of old-growth forests for Central Finland.

<p><strong>INTRO</strong><br> This archive contains data and analysis code for the Biodiversity Map -project conducted by Open Knowledge Finland (http://fi.okfn.org/projects/biodiversity-map/)</p> <p><strong>LICENCE</strong><br> The files listed below are all released to the public domain under a CC0 public domain dedication (https://creativecommons.org/publicdomain/zero/1.0/)</p> <p><strong>FILE DESCRIPTIONS</strong></p> <p><em><strong>FILE 1:</strong></em> background.zip<br> Inside the archive is a comma-separated file "background.csv" containing LiDAR-derived forest structure variables for 2/3 of Central Finland. These were derived from 3 raster data sets describing forest canopy maximum height (mh), forest canopy cover (cc) and lidar return intensity (in). The rasters had resolutions of 6 metres, 6 metres and 2 metres, respectfully. An 18 m resolution grid was then used to aggregate the rasters into average, minimum and maximum values + standard deviations of the original variables. The original LiDAR data was made available by the National Land Survey of Finland.</p> <p><br> <em><strong>FILE 2:</strong></em> conservation.lambdas<br> This file contains fitted parameters for the maxent model. For more information, check maxent documentation at https://www.cs.princeton.edu/~schapire/maxent/</p> <p><strong><em>FILE 3:</em></strong> conserved_swd.csv<br> Forest structure variables at 18 meter resolution for old-growth conservation areas in Central Finland. A subset of background.csv. This file still has a header, the variables are the same as in background.csv</p> <p><em><strong>FILE 4:</strong></em> grass_create_forest_rasters_from_las.sh<br> A shell script used to convert LiDAR files to raster maps of forest structure with GRASS 7.</p> <p><em><strong>FILE 5:</strong></em> lidar_coverage.png<br> A map showing the extent of LiDAR data available for Central Finland when we did the analyses.</p> <p><em><strong>FILE 6:</strong></em> maxent_model_run_product.sh<br> A shell script used to fit the maximum entropy model to predict the locations of conservation-area-like forests in Central Finland.</p> <p><em><strong>FILE 7:</strong></em> projection_product.csv<br> The results of the maxent model in a comma separated file. The first row has the variable names: x,y,product_fit. x and y are coordinates in the CRS ETRS-TM35FIN (EPSG:3067). product_fit is "the probablility that this 18*18 meter grid cell is old-growth conservation area".</p> <p><em><strong>FILE 8:</strong></em> README<br> A file with a description of the dataset in human-readable form.</p> <p><strong>VALIDATION FILES</strong><br> The data in these files was collected to validate the results of the aforementioned maxent model. The data were collected in a hierarchical sampling scheme: six randomly determinded unintersecting 9 km * 9 km landscape windows were chosen for sampling. From each window, three samples were taken. One sample from conservation areas, one sample from the "best" 10 % of forests as determined by the maxent model excluding conservation areas and one random sample. Not all windows contained conservation areas, and not all areas were accessible (islands, for example). In addition a few areas were skipped due to time constraints.</p> <p>The sampled points are identified by their lanscape window (suuralue), their sample (otos) and their sample number (mittauspiste).</p> <p><em><strong>FILE 9:</strong></em> validation_felled.csv<br> A comma separated list of those points that were not measured because they were felled.</p> <p><em><strong>FILE 10:</strong></em> validation_gps_results_2016-09-07.csv<br> A list of gps coordinates for all the sample points. product_fit is the value of the geographically closest prediction from the maxent model described above.</p> <p><em><strong>FILE 11:</strong></em> validation_lying_deadwood_transects_2016-08-30.csv<br> A comma separated file with data from deadwood transects. From each validation point, three 30 m long transects were made with 120 degree angles between them, and all lying deadwood more than 2 cm in diameter were measured. For some validation points, there were geographical obstructions which prevented the full 90 m of transect being surveyed, this is also recorded in the data. Each row holds measurements from one lying trunk.<br>  </p> <p><em><strong>FILE 12:</strong></em> validation_relascope_2016-08-30.csv<br> Relascope measurements from the validation points. Each row is measurements for one species from one validation point. Dead and alive trees are counted separately.<br>  </p> <p><strong>MORE INFORMATION</strong></p> <p>For more in-depth descritions of the files, read the file named README.<br> For some auxilliary files and information, check our old hackathon repository on github: https://github.com/Koalha/bdm_hackathon</p>

opencc-zeroOct 2016View details →
dryad40/100

Data from: The effect of drainage on the fine root biomass, production, and turnover in hemiboreal old-growth forests on organic soils

<p>Information on the capacity of organic soils to capture and store carbon in old-growth forests in the hemiboreal forest zone is scarce and fragmented. However, fine root data can provide valuable insights into soil carbon fluxes. Thus, the aim of the current study was to provide estimates of the fine root biomass (FRB), fine root production (FRP), and fine root turnover (FRT) rate by tree species and other functional groups in old-growth (stand age 131–179 years) forests on mesotrophic organic soils dominated by Scots pine (Pinus sylvestris L.), with (drained mesotrophic organic soil) and without (undrained mesotrophic organic soil) the effects of forest drainage. The sequential soil coring method was used to estimate the FRB and FRP. The total FRB (sum of the FRB of all functional groups) was significantly higher in the undrained sites (6.8±0.3 t ha 1) than in the drained sites (3.97±0.1 t ha 1). The FRB of Scots pine in the undrained forest was significantly higher (1.7±0.1 t ha 1) than in the drained forest (0.5±0.1 t ha 1), supporting an extensive foraging strategy. The significantly higher mean FRB of Norway spruce (Picea abies [L.] Karst.) (1.4±0.1 t ha 1) in the drained sites than the undrained sites (0.7±0.2 t ha-1) can be explained by there being a higher proportion of spruce in the stand compositions, thus a higher standing volume (cubic meters per hectare) of this species and an increased FRB. The FRB of dwarf shrubs (2.43±0.2 t ha-1) formed the largest part of the total FRB in the undrained sites and the second largest (1.16±0.1 t ha-1), following Norway spruce, in the drained sites. The total FRP was similar between the undrained (2.05±0.31 t ha-1 yr-1) and drained (1.82±0.26 t ha-1 yr-1) stands. However, considerable variability in the FRP was observed between different sites of the same forest site type. The FRT rate of Scots pine was twice as high in the drained sites than the undrained sites, suggesting faster nutrient and carbon input into the drained soil compared to the undrained soil. Estimates of FRB, FRP, and FRT rate for different functional groups can be used in carbon-cycle modeling and in further calculations to estimate the carbon budget (balance) in forests on organic soils.</p>

opencc-zeroFeb 2024View details →
zenodo40/100

Data for "Impact of early cleft lip and palate surgery on maxillary growth in 5- and 10-Year-old patients with unilateral cleft lip and palate: a cross-sectional study"

<p>Relative frequency in % (absolute frequency is shown above each bar). Frequency of 5YO indices in cleft patients and frequency of GOSLON indices in cleft patients.</p>

opencc-by-4.0Jul 2024View details →

ScienceDex guides

Understand access before you commit

These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.

Compare curated datasets

Allen Brain Atlas

Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

Annotated Behaviour and Observability Dataset (ABODe)

ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

DANDI Archive for NWB datasets

DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

International Brain Laboratory public data

The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

OpenNeuro

OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record