Marine biology
Albatross
Annelid
Tunicate
Sea anemone
The muscles and nerves in anemones are much simpler than those of other animals. Cells in the outer layer (epidermis) and the inner layer (gastrodermis) have microfilaments grouped together into contractile fibers. These are not true muscles because they are not freely suspended in the body cavity as they are in more developed animals. Since the anemone lacks a skeleton, the contractile cells pull against the gastrovascular cavity, which acts as a hydrostatic skeleton. The stability for this hydrostatic skeleton is caused by the anemone shutting its mouth, which keeps the gastrovascular cavity at a constant volume, making it more rigid.
Mollusca
Sponge
Echinoderm
Dinoflagellate
Dinoflagellates have a complex cell covering called an amphiesma, composed of flattened vesicles, called alveoli. In some forms, these support overlapping cellulose plates that make up a sort of armor called the theca. These come in various shapes and arrangements, depending on the species and sometimes stage of the dinoflagellate. Fibrous extrusomes are also found in many forms. Together with various other structural and genetic details, this organization indicates a close relationship between the dinoflagellates, Apicomplexa, and ciliates, collectively referred to as the alveolates.
The chloroplasts in most photosynthetic dinoflagellates are bound by three membranes, suggesting they were probably derived from some ingested algae, and contain chlorophylls a and c and either peridinin or fucoxanthin, as well as various other accessory pigments. However, a few have chloroplasts with different pigmentation and structure, some of which retain a nucleus. This suggests that chloroplasts were incorporated by several endosymbiotic events involving already colored or secondarily colorless forms. The discovery of plastids in Apicomplexa have led some to suggest they were inherited from an ancestor common to the two groups, but none of the more basal lines have them.
All the same, the dinoflagellate still consists of the more common organelles such as rough and smooth endoplasmic reticulum, Golgi apparatus, mitochondria, lipid and starch grains, and food vacuoles. Some have even been found with light sensitive organelle such as the eyespot or a larger nucleus containing a prominent nucleolus.
Diatom
Tide pool
Seagrass
Seaweed
Aquatic plant
Brown algae
Ocean
Coralline algae
Red algae
Algae
Algae lack leaves, roots, and other organs that characterize higher plants. They are distinguished from protozoa in that they are photosynthetic. Many are photoautotrophic, although some groups contain members that are mixotrophic, deriving energy both from photosynthesis and uptake of organic carbon either by osmotrophy, myzotrophy, or phagotrophy. Some unicellular species rely entirely on external energy sources and have reduced or lost their photosynthetic apparatus.
Golden algae
The golden algae or chrysophytes are a large group of heterokont algae, found mostly in freshwater. Originally they were taken to include all such forms except the diatoms and multicellular brown algae, but since then they have been divided into several different groups based on pigmentation and cell structure. They are now usually restricted to a core group of closely related forms, distinguished primarily by the structure of the flagella in motile cells, also treated as an order Chromulinales. It is possible membership will be revised further as more species are studied in detail. They come in a variety of morphological types, originally treated as separate orders or families.
Most members are unicellular flagellates, with either two visible flagella, as in Ochromonas, or sometimes one, as in Chromulina. The Chromulinales as first defined by Pascher in 1910 included only the latter type, with the former treated as the order Ochromonadales. However, structural studies have revealed that short second flagellum or at least a second basal body is always present, so this is no longer considered a valid distinction. Most of these have no cell covering. Some have loricae or shells, such as Dinobryon, which is sessile and grows in branched colonies. Most forms with silicaceous scales are now considered a separate group, the synurids, but a few belong among the Chromulinales proper, such as Paraphysomonas.
Some members are generally amoeboid, with long branching cell extensions, though they pass through flagellate stages as well. Chrysamoeba and Rhizochrysis are typical of these. There is also one species, Myxochrysis paradoxa, which has a complex life cycle involving a multinucleate plasmodial stage, similar to those found in slime moulds. These were originally treated as the order Chrysamoebales. The superficially similar Rhizochromulina was once included here, but is now given its own order based on differences in the structure of the flagellate stage.
Other members are non-motile. Cells may be naked and embedded in mucilage, such as Chrysosaccus, or coccoid and surrounded by a cell wall, as in Chrysosphaera. A few are filamentous or even parenchymatous in organization, such as Phaeoplaca. These were included in various older orders, most of the members of which are now included in separate groups. Hydrurus and its allies, freshwater genera which form branched gelatinous filaments, are often placed in the separate order Hydrurales but may belong here.
Chrysophytes were once considered to be a specialized form of cyanobacteria containing the golden-yellow pigment, fucoxanthin. Because many of these organisms had a silica capsule, they have a relatively complete fossil record, allowing modern biologists to confirm that they are, in fact, not derived from cyanobacteria, but rather an ancestor that did not possess the capability to photosynthesize. Many of the chrysophyta precursor fossils entirely lacked any type of photosynthesis-capable pigment. Most biologists believe that the chrysophytes obtained their ability to photosynthesis from an endosymbiotic relationship with fucoxanthin-containing cyanobacteria.




















