Phacus orbicularis Hübner 1886 from a sample fed with boiled wheat seed from the edge benthos of freshwater glacial kettle hole Kellis Pond. Imaged in Nomarski DIC on Olympus BH2S using SPlan 100 1.25 oil objective plus variable phone camera cropping on Samsung Galaxy S24.
The cells measure from 46 up to 52 um in length. The s[pepcies was firsts described by Hübner 1886 (1). We can clearly see the horizontal "struts" perpendicular to the longitudinal pellicular strips first described by Lefevre in 1931 and, after much confusion see (2) felt by Kozmala et al 2007 to be the distinguishing character for P. orbicularis (2).
"Species. Ph. orbicularis n. spec. My illustration Fig. 1. Body is almost circular, not painted at the front. The crooked torsion is very developed, the body appears flat. The mouth fold only leads to a slight upward bulging of the dorsal ligaments. The abdominal area on the right side (back view) is visible at the top, but it does not cause any abnormal curvature of the back area. Cuticle delicately striped. Chromatophores, cell nucleus, main vacuole according to the genus character. A large granule in the shape of a disc with a central opening, resting on the ventral surface, in front of or behind the cell nucleus. Terminal spine clearly visible, 1:6 of the body length, pointed left and upwards (back view). Flagellum of body length. Size = 0.07 mm. end spine. Br. = 0.045 mm. Occasionally, among other Euglenaceae, bird meadows" (1).
"Phacus orbicularis Hübner, Programm d. Realgymnasiums Stransund: 5, fig. 1, 1886. Emend. Zakrys´ et Kosmala. Emended diagnosis: Cells flat, 29–75 um long and 22–49 um wide, widely ovoid, ending with a more or less prominent and curved tail. Fine, numerous struts—perpendicular to the longitudinal axis—located between periplast strips" (2). "Periplast ornamentation was recognized as a main diagnostic character, distinguishing P. orbicularis from P. pleuronectes and P. hamelii. Phacus orbicularis has struts running perpendicular to the longitudinal axis of the strips, while P. pleuronectes and P. hamelii do not" (2). Support for this morphologic character being distinctive to P. orbicularis among congeners: " On the SSU rDNA tree, obtained by the Bayesian method, P. orbicularis, P. pleuronectes, and P. hamelii belong to three distinct clades" (2).
"Our studies also point out periplast ornamentation, described as ‘‘struts’’ by Leedale (1985), which are positioned perpendicular to the longitudinal axis of the strips. The struts were present in all P. orbicularis strains surveyed by us (Fig. 1, n and u)— all SSU sequences for the P. orbicularis strains clade together on the 18S rDNA tree (Fig. 2)—but struts were not observed in P. pleuronectes or P. hamelii (Fig. 1, o and t). Lefevre (1931) was the first to notice ‘‘perpendicular stripes’’ in P. orbicularis and take them into account in his drawings. Lefevre’s drawings were used later by Pochmann (1942, fig. 78, k and n), albeit without any commentary. This action suggests that both Lefevre and Pochmann, as well as others, did not consider struts to be a diagnostic feature distinguishing P. orbicularis from P. pleuronectes. This also might be the reason for not considering struts as diagnostic in spite of their appearing on drawings of several other species (P. rostafinski [Drezepolski _ 1921 ⁄ 1922, pl. 1, fig. 3]; P. platalea [Drezepolski _ 1925, pl. 3, fig. 110]; P. caudata var. minor and var. ovalis [Drezepolski 1925, pl. 3, figs. 107 and 111]; _ P. longicauda [Lefe´vre 1931, pl. 3, fig. 32]; Phacus triqueter [Leander and Farmer 2001, fig. 3a]). The presence of perpendicular struts on the iconotype of P. platalea Drezepolski 1925 (fig. 110), as well as its _ other features, such as the size and shape of the cell and the relatively long (12–15 lm) tail, prompted us to consider P. platalea as a synonym of P. orbicularis. In our view, the presence of struts is a good diagnostic feature for distinguishing P. orbicularis from P. pleuronectes since it is not susceptible to individual, developmental, and environmental variability. Moreover, struts are clearly visible under the light microscope, even in very small cells (in which case, a brief drying out of the material facilitates observations; Fig. 1, n and u)" (2)
Mateola is an endemic desmid genus from the Tropical region of American continent
A Tropical variety of Micrasterias torreyi
Proliferaron en una muestra de musgo sumergido en agua
Specimen rolled over partway through the observation, allowing a nice observation of two aspects.
Marine sample gathered with a 20µm net.
Time 10:15 AM
Weather: Clear, Sunny
Air temp: 11C
Water Temp: 9C
Salinity: 35ppt.
Wind: 0-10 NE
Tide: Approximately 2.0 ft. Incoming
Secchi depth: 340 cm
Reproduction by budding, or is it division?
Time 9:40 AM
Weather: Cloudy
Air temp: 10C
Water Temp: 12C
Salinity: 33ppt.
Wind: 0-5 MPH, NW
Tide: High tide, 6.67ft. (King tide)
Secchi depth: 340 cm
Mag. 400x
Longish (200µ). U. piscis? Looks like 3 rows of ventral cirri... diagnostic?
@bdstaylor, @shanesmicroscope, @crseaquist
Mag. 400x (1), 100x (2,3)
Somewhat evenly spaced clusters of yellow-brown cells on a strand of Eunotia sp. cells. Algal epiphytes? Egg deposits?
Mag. 400x (freshwater)
Uniformly oval. Regularly spaced spikes. There is also a smaller spike-covered object (rod shaped?), just behind or in front of the large oval. (I can't tell where the focal plane is sitting.) The smaller object is visible in the lower panels of the photo composite, image 2. If the primary object is an egg case, what is the smaller spiky object? Perhaps the smaller object is a peal projecting from the large oval...like projecting panel from an opening chestnut. Interesting!
Mag. 400x
13 dorsal margin undulation. As seen here https://diatoms.org/species/eunotia_serra. (note: this taxa can have 6-22 dorsal margin undulations)
Mag. 400x (1,2), 100x (3)
Time 3:30 PM
Weather: Clear
Air temp: 12C
Water Temp: 8.5C
Salinity: 34ppt.
Wind: 10-20 MPH, NNE
Tide: High tide 2.95
Secchi depth: 340cm
A stream water sample (freshwater) was taken on 11/06/2021 using a 10 micron dip net to enrich for microorganisms.
Moved 50-100µm in less than a minute.
Philodina laying an egg. For some reason the Dexiotricha were very interested in the proceedings.
A pond edge water sample (freshwater) was taken on 10/19/2021 using a 10 micron dip net to enrich for microorganisms.
Mag. 400x
Each spine is rooted in a circular scale (photo 2). Circular egg (photo 4)?
A pond edge water sample (freshwater) was taken on 10/14/2021 using a 10 micron dip net to enrich for microorganisms.
Collected from a freshwater pool in the Ecology and Evolutionary Biology Greenhouse.
Mag. 400x (1, 4gif,6), 100x (2,5), 25x (3)
By far (>95%), this was the predominant specie netted during this collection... a bloom of C. longispina. Each cell has several, long siliceous spines and 2 flagella (one short, one long) http://www.diatom.org/lakes/taxa/chryso/Chrysosphaerella/TB-Chrysosphaerella_longispina.htm. Image 3 is a gif; careful inspection will show flagellar movement. -- The slide was allowed to dry and then reexamined after several days, see image 5. The drying process appears to have released some of the spines from the cells. Their double-headed nail-like structure is apparent in image 6 (also see http://cfb.unh.edu/phycokey/Choices/Synurophyceae/CHRYSOSPHAERELLA/Chrysosphaerella_Image_page.html)
A pond edge water sample (freshwater) was taken on 10/14/2021 using a 10 micron dip net to enrich for microorganisms.
A sample of seaweed collected from the beach at Ocean City, NJ.
Mag. 400x
16-cell colony. Each cell is tethered to a single stalk that converges, by tetrachotomous branching, in the center of the colony; there are 4 cells at the end of each major branchlet. The bottom frame in the composite photo (last photo) best shows the branching system. Compare to images here https://www.algaebase.org/search/species/detail/?species_id=176802&sk=0&from=results.
A pond edge water sample (freshwater) was taken on 10/1/2021 using a 10 micron dip net to enrich for microorganisms.