Silvaconrepo culcitae and the phylum of Quadrachordates

 Silvaconrepo culcitae is a quadrachordate which slithers around the Tuaisceartan TDTLF biomes. It is part of a forest-dwelling chordates who have adapted their locomotion to slither across the forest floor. This particular species eat up dead leaf litter exclusively. It is around 40 mm long . They are hunted by bigger organisms, such as articulusids and mollisids which traverse the forest floor for food. 

A loose illustration of a specimen traversing

A quadrachordate is a phylum of apothemaites who have evolved from slow-moving organisms which inhabited tidal areas of the Eilen coasts. They can be compared to echinodermata of Earth, but they have many differences. 

Quadrachordates are both sea-dwelling and land-dwelling apothemaites. Originally possessing radial symmetry, they were sessile organisms who had a mutation which caused them to store calcium deposit in four so-called "spinochords" . The spinochords would eventually get segmented and flexible as the organisms of the phylum got more motile. Developing complex structures in order to aid in faster locomotion(as to invade larger sea predators) and developing their visual senses, (developing compound eyes, for examples ) . They would use the unpredictable tidal zone areas for the safety. This would cause many quadrachordates to get dried on the beaches of Eile or stuck in smaller pools. Eventually, this hard-wires the quadrachordates to last longer on land. 

They would develop spiracles and small pseudo-lungs lined under the layer of their skin in the center disk part of the body  to process oxygen from the fresh Eilen air. They would invade the lands and establish their own niches like everyone else on Eile. 

Silvaconrepo culcitae and members of the clade it is part of have structures under the lower quarter of their "legs", these are loose, small fibrous which allow to sense vibrations  around it and can stiffen to aid in traversing rougher terrain in the forest floor. 

Thanks for reading.

Spotted Giblitka

 The organism we are looking at today is the Spotted giblitka, scientific name Magnagibber crudaangulus EILE . It is part of the motiloid phylum, Eumollisids, a topic which has only been briefly discussed beforehand. 

Eumollisids are truely a special type of phylum in Eile. Being older than the articulisid phylum and all apothemaite phylums. And being in early eons of multi -cellular life. 

Eumollisids are still quite significant today. From "worms" to "snails" to "pseudo-sea snakes", they are an incredibly diverse and adaptive phylum which may show mechanisms behind further advanced motiloid evolution to apothemaites and even more.

The species in general is part of a larger group called Gibberids, some may compare them to the gastropods of Earth , Gibberids use internal structures in order to produce locomotion and be able to move. Those internal structures are modified miniscule muscles enabling Gibbberids to move across the bumpy surface of the forest floor.

This organism (the Spotted Giblitka) traverses across the forest floor looking for leaf litter, sometimes, it will consume "eggs" that are attached onto the leaf litter that are left attached on the leaf. Sometimes these eggs can be a good nutritious meal, or cause a parasite to grow in their bodies(causing them to die as the organism develops more and more inside of them). The spotted giblitka is gonochoric, with males being brighter green and smaller, while females being duller green and bigger.Also having specialised reproductive organs for each sex. The female lays hundreds of small jelly-like eggs, only 1 in 100 eggs pass through the hatching stage. However, if they do hatch, most of them survive to adulthood and beyond, living for around a good 10 years. Thanks for reading as always and see you in the next post.

Sessile Organisms of the Tuaisceartan Forests

OOC: Hello, this post is going to be more of a proper post for Eile this time around. I have decided that I am going to refer to photosessilids as photoids/flora from now on.  Euheterosessilids as Eusessiloids/funga, and the Heteromotilids as motiloids/fauna from now on. Reason being to be more concise while trying to make it clear that That doesn't mean that the names for the Kingdoms of life have changed, however.

Greetings, everyone! Today we are focusing on sessile organisms which inhabit the forests of the TDTLF biomes.  TDTLF biomes for a quick explanation are necessarily mainly forest habitat with some plains contained inside it that continues after the range of a denseforests, although this isn't necessarily the case for every TDTLF habitat, it is, on Tuaisceart. 

A "forest"on Eile is defined by the dominance of tree-analogues. They contain a variety of organisms, despite being dominated by these towering tree-analogues. 

Most tree-analogues on Eile have to communicate in order to decide metabolic cycles and best times in order to loose leaves and other things. While this was said on the last post, we are going to be exploring this further on the habitats of Tuaisceart. Trees often have to communicate with sometimes completely different tree-analogues and in order to complete this they have to have symbiosis.  Symbiosis can often be hijacked, which forces symbiotes to evolve further, the hijackers adapt to these changes, an evolutionary arms race begins. Let's look at these tree-analogues.

.

A sketch of a Cranya next to a stickman for size comparison, this tree analogue is a very typical one in Tuaisceart's TDTLFs, core and roots are extended and meet with "hyphae" treads of the eusessiloid organisms. The tree top half is especially confusing, some "tree-analogues" never developed any kind of symmetry. The Cranya branches and leaves are easily regrowable due to being rather flimsy structures. Despite this, they are often host to variety of organisms and organism-made structures over their long lifetime(130-140 Eilen years)Colonies, nests, parasites make this organism their home. Reproduction is also made through releasing pollenoids, however this time reproduction is more akin to a pine tree despite radically different morphologies . Releasing two fruiting bodies, one male, and one female, the female one is hard like an acorn, while the male one is soft and spongy. The male fruiting bodies releases pollenoid to other cranya trees female fruiting bodies through wind ( Eile has lower gravity, making it easier to traverse through wind), occasionally use of fire and some kind of heat was evolved as an alternative to spread the pollen. The female fruiting bodies once the pollenoids enters them, they fertilize into a "nut" and become so heavy that they drop down into the forest floor, where wandering organisms will eat and excrete the seeds out in a lucky enough location. All of this results in a new cranya "tree-analogue". The scientific name for the species is Confususmateriae confususmateriae EILE.

Here is some sketches of tree-analogue that can be found on Tuaisceartan forests,these show the variety of morphologies that can be found. The number to indicate what is what is below each tree.

1. A pine-like species of tree-analogue found in forests. Often a shelter or place for organism-made structures. Evolved from isolated species.

2.Perhaps more of an "undergrowth" tree-analogue, maybe related to the Cranya.

3. Bizzare tree analogue, also a great shelter for species, perhaps related to 1.

4. An uncommon tree-analogue which has an unusual shape and form.

5.A tree-analogue that looks like a spruce, however, not "evergreen"

6. The most special about this one in that it has the most secure "network attachments" between the eusessiloids in the ever growing arm race between saboteurs and symbiotes.

7. Produces large fruits which taste like somewhere between a tomato and an apple.

8.A monstrous tree analogues which reproduces using motile "gametophytes". This tree acts as a hub for pseudo-mycorrhizal networks and communication between trees.

9. A strange tree-analogue which roots itself using "hyphae".

10.Perhaps related to 9. , considered more as an undergrowth photoid, however it still communicates with other "trees" using the networks. 

Moving on from these photoids, are the eusessiloids. 

The Eusessiloids/funga of these "forests" are the powerlines and wires of a vast biological network. The energy and pumping between these can cause soil temperature to rise, making a land forest on Tuaisceart that is sometimes hot. 

This is basically a biological mini-powerline. Also, first look into one of the many Eusessiloids on Eile. This Eusessiloid is part of a phylum which had adapted to land, it is the analogue of the complex multicellular fungi found on earth, however, the shape of them are indeed, radically different. The purple bulb contains a clump of tubes and vessels pumping around collections and information between the big organisms of the forest. This also contains practically biological neural cells in order to organise the direction of which and what information is going. These organisms take around 30% of the energy that is sent between the"tree-analogues" for their own growth, sometimes, if there is a lot information being sent between, it can even take 60-70% of energy transmitted. The yellow structure is a spore "transmitter", containing sporomytes which are motile, microscopic, and move until they find an smaller untaken patch. Once found, they"germinate", unmatured younger mini-powerlines often parasitize networks before becoming mature. Flavum violaceum EILE is the scientific name for this species.

Let's look at this red, wondrous bush, it is a parasite of the endless symbiosis. An endless arms race between symbiotes and saboteurs is evident within the sessile side of the world of Eile. A possible relative of the exarborigramenids(A group of woody photoids, often with tree analogues), this photoid has assumed red leaves in order to gain as much energy as possible from what light is left in these forests . However, as you can also see in this illustration, it that it parasitises "mycorrhizae" and "roots" of connected networks, taking 80% of the nutrients and "information" being sent ,practically causing biological  "network disruptions" to occur. These reproduce asexually and through spores through the top "leaves" of the photoid. Rubrum tuaisceart EILE is the scientific name for the species illustrated.

2 Illustrations

 

OOC: Hello everyone this is a post simply demonstrating some landscapes I made digitally and simple explanation on what is going on.I have tried something new in both of them so feel free to give feedback or ask questions. Next post will be focusing on individual organisms again.Both illustrations apply to the TDTLF biome in Tuaisceart.Some of the organisms mentioned here will probably be in the next post and expanded on further.

An Illustration of some of the photosessilids of the TDTLF in  Tuaisceart, Forests in the distance are represented  by the green cage-like mounds, this does not mean  necessarily that "trees" have green wood,or leaves same colour as their wood.(Although some have subtle green shades). These illustration represents a TDTLF plain somewhere in  Tuaisceart. Classic grass analogues, which are ancestors of trees found in denseforests and TDTLFs , usually dominate the plains, These plains are usually small and found on "ecotones" of plategrass biomes, And an abundance of small plants that wouldn't be able  to grow on the "wooden" plains of plategrasses are found here. As illustrated here, small plants with droopy leaves called Dripleaves  are found in variety of green shades.

An Illustration of the forest floor of some understory sessile organisms, leaf litter and branches from Eilen "trees" of the TDTLF biome  forest habitat are scattered here. As we can see here.Two yellowish sessile organisms, who have emerged from underground in as fruiting bodies, these are euheterosessilids. Trees of this type on Eile can grow their leaves back, and often loose leaves,much like deciduous tree on ,they don't loose leaves pattern-wise, due to Eile's seasonal  and weather changes, having to rely on symbiosis of sending metabolisms through euheterosessilid's hyphae, which can be hijacked by the understory photossessilids, such as the Drapleavebush ,shown as the understory photosessilid in the illustration , with droopy leaves,which connects via hyphae-like threads   . Leaves are many and are small due to this. On average, "Trees" on Eile are taller, and looser by a  marginal amount, there are exceptions although we won't expand on that for today. There is some small "moss" growing on the trees as well.

Thickarmour Lightfly, Yellowcrest and Redlobe Astyels

Hello, today we are going to focus on flying organisms of Eile, specifically the temperate plains biome in Tuaisceart. These flying organisms have habitats that change often because of micro-migration. Thus making these organisms "inter-biomal". 

The larger flying organisms of Eile are mainly the articulisids and Apothemaites, specifically Katoikosaeras, a polyphyletic group of Appendixaforms which have evolved to fly. Unlike the term birds on earth,a katoik(Katoikosearan for short) may refer to any of classes of appendixaforms that evolved flight.

Flying organisms on Eile in general evolved from some kind of small plain dwelling or semi-plain(plains in TDTLF biome ) dwelling descendant, whether it'd be an articulusid or a Katoikosaeran. Using extended vein lobes or articulated wings as acceleration before eventually evolving to use air currents and wind direction in order to accelerate even further , thus achieving flight. Once achieved flight, the organisms evolved and repurposed their bodyplans for occupation of the many niches flight can offer. 

Due to lower gravity and thinner atmosphere, flying organisms are smaller on average then earth organisms,yet are able to stay on air longer on average due to lower gravity, as it is easier to retain flight, but harder to launch into the air. 

Katoikosaeras are appendixaforms, since appendixaforms are apothemaites(vertebrate-like on Eile), Katoikosaeras convergently utilize some aspects of earthen traits in their morphology, albeit rather loosely. Some Katoikosaeras have evolved an independent form of viviparity from the rest of the appendixaform group (many other appendixaforms are viviparous) .

We will explore some of these morphologies of flying organisms on Eile through 3  different organisms.

The Thickarmour lightfly is a microscopic, small flyer which are part of the articulusid phylum, they are part of a large clade of flying organisms called Sexartusmuscae , who are winged articulusids which evolved from hexapodal lineages. 

They are bloodsuckers, and not greatly sexually dimorphic, with only ever so slight differences in physicality between males and females. They are armoured as they are predators who actually scavenge for them. Thus quicker reproduction becoming a necessity in the species.

Illustration of Thickarmour Lightfly , The orifice
 at  the front,as well as the green appendage have evolved different roles, the green appendages has evolved into  a tube for sucking blood  and other liquids, a liquivorous diet only feasible for much small  organisms like itself,whilst the orifice has the role of helping with breathing. This illustration depicts a specimen clumsily walking along a tree branch, which is a mating behaviour that can be found in Thickarmour lightflies but is very random, tree branches or any solid area can be used as mating grounds.Like most articulusids in the temperate plains, these small organisms are much active in dawn and dusk. The scientific name for these organisms are Brunapinna ruberscutum EILE. In the top left, there is an illustration of the top side of the organism when it is flying.

Next up we have the Katoikosaeras. Yellowcrest atsyel and Redlobe atsyel are species of the same family,called Quantulacibidae .They're relatively small species, no larger then a tit when standing on their two legs, even smaller when flying,the naming behind atsyel is a chunk taken from the transcripted Russian word lyetatsyel'. And then "Redlobe" and "Yellowcrest" have been taken from their appearances. 

Yellowcrest and Redlobe flying through tree branches. Leaves were not illustrated here in order to show organisms In reality, they would all be covered in leaves.

The scientific name for Yellowcrest is Folirumpere fulvathorax EILE and the scientific name for the Redlobe is Foliumimpello cruentacaput EILE. Both apothemaites are part of clade of Katoikasaeras  in which bone structure changed drastically,  evolving from early more "bird-like"( four legs ,two wings) into an entire separate class, called Suprapenna , Whose wings are over the legs. This was an incredibly slow evolution , thus most of the class having still undeveloped clades as this is a recent morphology.  The skin of such lying organisms in this clade is lined by many, many hairs, similar to those of bat and pterosaurs,  however much lighter, and much more.

The Yellowcrest's an Redlobe's bright colours may be a form of false aposematism to try and detract predators, as larger apothemaites do hunt these organisms. While the Yellowcrest and Redlobe are similar organisms, with similar behaviours, such as thrusting through the leaves trees of the temperate plains and making nesting grounds of them.They have different enough niches which allows them to prevent competition. The yellowcrest is most times frugivorous, as it is difficult to be an obligated on the plains. The Redlobe is most time articuluvorous( eating articulusids,insect-analogues of Eile.), basically vice versa. 

This is it for today's Eile post, thanks for reading! 

Golden Liners and Bananacoloured plainsrunners

 Hello everyone, today in this entry we are going to look at Golden Liners and Bananacoloured plainsrunners, these are some of the species which roam the endless temperate plains . These are also, interestingly, some of the first Vertebrate-analogues(which are called apothemaites, although not all apothemaites are "vertebrates"on Eile) we will be looking at in this entry. So in reality, I am saying these are only some of vertebrate-analogues that roam the temperate plains.

The Golden Liners are part of the dyopod clade.The Dyopodia are apothemaites defined by having only two limbs, which as a result, made Dyopodia have developed vestibular and neural systems but a lack of head, often the tail is evolved from coverings of the genitalia, which were prehistorically nozzle growth which served as sexual organs, this phenonmenon in development of tails as a result of needing cover the sexual organs is common in other "vertebrapothemaites"( Vertebrate-like apothemaites, which Appendixaforms, Caputicentralisids & Dyopods are part of ). The Golden Liners belong to the order of campestrids. Campestrids are a widespread order of dyopods who evolved to live on the plains, savannahs, and other biomes of flat ground. Dyopodia have 4 stalk eyes and small opening in each sides of their body in order to let air into their system and allow respiration and respiratory metabolic processes (such as breathing) . The eyes are semi-silicate and use partially liquid so they only require slight shedding now and then, the eyes quickly recover from the shedding, especially in the Golden Liners as it required in their vision to stay wary of predators at all times. They hear through "ears" which function similar to ears in apes and mammals,picking up vibrations and transmitting into electric signals which produce different sounds at different frequencies and pitches based on how the "ear" is vibrated. The ears is on the side of their bodies.

Above is pictured an illustration of a Golden Liner grazing. Dyopods in general or known for their strange almost-cubical appearance. However this form has proved useful for many dyopods. Some have evolved a bipedal retrograde stance or a typical theropodal stance. The yellow appendages growing in the front are olfactory organs. Here we see as well an area of blades produced by plategrass that look less succulent than the ones found in previous illustrations, this must mean that the blades are new and still developing. This is an indicator that Golden Liners graze often in this area.

The scientific name for Golden Liners are Flavanasus fulvacrus EILE. Dyopodia, like Golden liners have retractable eyestalks which helps them see. They also can retract the long semi-proboscis mouth( which is essentially a jaw connected by a neck) if they are not digesting any food. The Golden Liner's are fursome grazers with an interesting look which makes them memorable to any who encounters them. Golden Liner often will eat eumollisids, articulisids and other kinds of unlucky ground-dwellers of the plain floors during the day as they graze the blades produced by plategrass.

The bananacoloured plainsrunners are predators which track down Golden Liners throughout the temperate plains. These are appendixaforms. Appendixaforms have some sensory appendages which are located differently and are used for different purposes, and are more related to the ancient caputicentralisids, thanks to their tetrapod-analogue features, however Appendixaforma like the Dyopodia had a different evolutionary history . 

The scientific name for Bananacoloured plainsrunners is Campestrevenator arienanasus EILE . The Bananacoloured plainsrunners possess powerful jaws to eat through the Golden Liners and are able to quickly manoeuvre them. However Golden Liners are able to reproduce rapidly in low specie population centres if the bananacoloured plainsrunners are not interested in a lack of specimens in the region.

Bananacoloured plainsrunners are able to aswell digest blades produce by plainsgrasses but not aswell as the Golden Liners. They have migration patterns between temperate plains and the TDTLF biomes in the continent of Tuaisceart.

Most Appendixaformes are and will be shown hexapodal in later entries, however this one is part of a newly evolved super-clade which has "tetrapodal" appendixaforms. These "tetrapods" have known to develop a whole bunch of various body types relatively recently compared to the well established almost ancient hexapods. However As we can see here, the two appendages at the top are for respiratory and olfactory functions, most "tetrapodal" and hexapodal appendixaforms have these. "Tetrapodal" appendixaforms have devolved their middle pair of limbs into a sort of other sensory appendages/ sexual display organs.Appendixaforms have similar ears and similiar olfactory organs to the Dyopodia. This plainsrunner is also in a developing field of blades.

Golden Liner and Bananacoloured plainsrunners compared in size to a slightly deformed human silhouette.

This is it for today's entry. Thanks for reading, I hope you enjoyed reading the article.

OOC: Hi everyone, I haven't done these in a while, the OOC section will be usually for notes and for anything I want to state "afterhand" and stuff. So first,  all images on the Eile blogpost website are made by me, with the obvious exception of the background image on it. Secondly, If you have any feedback to give or questions to ask, please do so :) . How plategrass' blades develop will be explored in later entries. There will (hopefully) be many alien plant spec and focus on individual plant species as I did for one of the previous articles so plategrass may be touched on again. This time I decided to post both articles at the same time just to try a new thing for this new entry. Again I thank you for reading.

The Articulisids of the floors of the temperate plains.

 In this entry we will be talking about the anapnoils(animal analogues of Eile), specifically members of the clade of Arthrotetrida , being the dominant clade of  land articulisids similar to how class Insecta is here of arthropods on earth. We will be talking about arthrotetrids on the natural pseudo-wood floors of the temperate plains, please note it will be only some of the species we will be talking about,it will be too long to count all species , and we will be mentioning about their families and inner clades to which they belong in.

Unlike the insects of Earth, the arthrotetrida of Eile possess four legs on which they walk on and possess internal support structures, however that doesn't mean they can get larger than arthropods or even insects for that matter. They have porous areas around their bodies which filters to breath  in air, which are linked to the mini-lungs and trachea systems around their bodies.

 The Arthrotetrids however have adapted to a wide range of body plans on land and using the advantages of their internal support structures have achieved unusual, unique, but highly useful bodyplans. They also have jaw pseudo-arms which feel similar to when you touch the flesh of a slug or snail, although they can feel dry and withdraw their slimy properties when it is time to consume food or manipulate the surrounding environment in order to consumer food. And some have changed the texture and feel to them using internal structures.

The first species we will be talking about is the Common Polkagreen,Punctiviriditis vulgaris EILE , it is a generalist biodetritivore and a waste decomposer. Primarily active at dawn. It feeds on biodetritus and waste produced by both the plategrass' and the apothemaites. Being active most at dawn and dusk, sometimes even into night as that is when they are less likely to get trampled by Eilen megafauna. This pattern of activity also applies to most arthrotetrid and "invertebrate" species who reside in the temperate plains. It is part of the Imitariscarabeiforms , a family of bio detritivores whose appearance is often reminiscent to that of beetles, albeit only at surface-level. They have a high level of diversity and can get pretty big for a purely land articulisid. They also have one jaw arm. The common polkagreens are 1cm tall and 4cm wide.

A common polkagreen walks along the blades. To a polkagreen, the blades produced the great colonial plategrass may seem like an endless forest. The polkagreen has an extendable jaw arm which can pass digestive enzymes if needed. Sometimes the other member of the Punctiviriditis genus , the Punctiviriditis cinismanduco EILE  loves to gorge istelf upon dead megafauna in "herds" up to 150 specimens of the species. Organisms to which the blades seem like a forest constitute a huge micro-habitat. 

The second species we will be talking about is the one who feeds on the cone shaped "blade" the plategrasses produce, the species, Acsendoprati vulgaris EILE , or simply, the Pygmy ditongue/  Greenplain blade-eater , although we will be using pygmy ditongues as the species is part of a family called pygmy ditongues with similiar herbivorous niches. The pygmy ditongue is part of the ditongues, a clade of arthrotetrids with protruding, sharp, claw-like jaw arms. The pygmy ditongue is , well a herbivore, as mentioned by the fact that it eats the blades of the Tuaisceartian plategrass .

The Pygmy ditongue has adhesive suction-like feet which are able to balance and stabilise and stick themselves onto the most unstable and flimsy of surfaces, such as the cone-shaped blade of the plategrass.

Like the polkagreens, these are also active mostly at dawn and at dusk, to avoid being trampled by the apothemaite megafauna, as so the majority of land articulisids in plains biomes. The pygmy ditongue is around 4mm in length. 

There are also organisms who predate on these critters, and they have a quite unexpected appearance only native to Eile. 

Plains blade-Pretender,  Imitor campestrecursor EILE., the specimen pictured here is among the low-growth blades, which grow about to it's size, being around 10cm tall.

The Plains blade-Pretender has a upper jaw arm, which is rather "pneumatised", and has developed complex internal structures  in order to be able to manipulate. The Plains blade -pretender takes advantage of the pygmy ditongues via using mimicry,  while the blade will look faulty and the pygmy ditongue will be hesitant, it will eventually decide that it just looks too good to give up and ignore .  Especially amongst lesser size blades, the blade-Pretender also has the advantage. Although they cannot be hiding in really short blades because even with the short-sightedness of the pygmy ditongues they may still figure. 

When a pygmy ditongues get on it's upper jaw arms, the blade-pretender will crush the pygmy ditongues absolutely cruelly, savouringly initiating every crush almost as if it is trying to play with it . But this is not true, simply the slow and meticulous crushing is a result of chitin armour of their prey, which results in larger force and energy being applied which have the blade-pretenders have evolved over millions of years to quickly excrete out of their bodies.

The Blade-pretender is part of the Superbrachiumids, an order of upper jaw armed species with high and diverse body plans. The Blade-pretenders long legs is because members of its family use mimicry in order to easily predate on the herbivores of the microhabitats.

As mentioned at the beginning of this entry there are many, many more species among the floors of these plains. But these are the ones that are mentioned in this article. Thank you for reading.