SILURIAN
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CLOSED
SILURIAN
443.1 - 419.2 mya
The Silurian is a period that lasts almost 24 million years, beginning after the end of the Ordovician period, 443.1 mya, and ending just before the start of the Devonian period 419.2 mya. The exact geological boundaries that define this period are well defined, but the exact dating of these boundaries are not totally clear. The Silurian period is characterized by a major incursion of terrestrial life, known as the Silurian-Devonian Terrestrial Revolution; even though complex life already was colonizing dry land in the Ordovician, it was in the Silurian where it truly began to flourish and thrive, with vascular plants evolving from more primitive terrestrial plants, diversification of terrestrial dikaryan fungi, as well as glomeromycotan fungi, and three distinct lineages of arthropods, the myriapod, arachnid and hexapod lineages, forming fully terrestrial forms.
The Silurian was first identified by the Scottish geologist Roderick Murchison, who examined rocks in South Wales in the early 1830s. Alongside his then friend, Adam Sedgwick, who named the Cambrian period, presented a joint paper in 1835, under the title of On the Silurian and Cambrian Systems, Exhibiting the Order in which the Older Sedimentary Strata Succeed each other in England and Wales, forming the basis for the modern geological time scale. There was conflict between some strata that overlapped Murchison's Silurian and Sedgwick's Cambrian, a conflict that terminated their friendship, and was resolved by Charles Lapworth who defined the Ordovician period to include the contested geological beds.
During the Silurian, the supercontinent of Gondwana covered much of the equator and southern hemisphere, with a large ocean covering most of the northern half of the globe; the period was divided by four epochs, starting with the Llandovery epoch, itself divided in three ages, the Rhuddanian (443.1 - 440.8 mya), the Aeronian (440.8 - 438.5 mya) and the Telychian (438.5 - 433.4 mya), the Wenlock epoch, itself divided in two ages, the Sheinwoodian (433.4 - 430.5 mya) and the Homerian (430.5 - 427.4 mya), the Ludlow epoch, itself divided in two ages, the Gorstian (427.4 - 425.6 mya) and the Ludfordian (425.6 - 423 mya), and finally the Přídolí epoch (423 - 419.2 mya).
During the Silurian period, the Earth was entering a warm greenhouse climate, with high CO2 levels and warm shallow seas covering much of the equatorial land masses. The climatic and carbon cycles were rather unsettled in the Silurian, indicating a lot of climatic fluctuations, more than any other period, inevitably causing frequent extinctions across its time.
The Silurian is the earliest period where we observe extensive terrestrial fossil biotas, a product of the Silurian-Devonian Terrestrial Revolution, with miniature forests of moss-like plants growing next to freshwater courses, with networks of large mycorhizal nematophytes. The second half of the Silurian is marked by the first fossil appearance of vascular plants, that is, plants with tissues that can carry food and water over a stem, allowing plants to grow taller and sturdier. One of the earliest fossil representatives of the vascular plant lineage were members of the genus Cooksonia. Around the Ludlow and Přídolí epochs we also start to see a diversification of terrestrial arthropods such as millipedes, centipedes and trigonotarbid arachnids. In the water, the fauna was adapting to the aftermath of the Late Ordovician mass extinction (LOME), such as brachiopods, the surviving lineages of which demonstrated novel adaptations for environmental stress, often being endemic to a specific locality in the globe before slowly expanding and diversifying elsewhere. Bivalve mollusks also diversified immensely in this period, and the first deep-boring bivalve fossils are recognized from the Silurian. Hederellids, colonial animals that may be related to our present's phoronids, diversified immensely in the Silurian, sometimes forming symbiotic relationships with colonial rugose corals. Among crinoids, the monobathrid camerates and flexibilians were diversifying in the Llandovery epoch, while cyathocrinitids and dendrocrinids diversified in later parts of the Silurian. Reef abundance was patchy across the period, sometimes fossils being very frequent and other times being virtually absent from strata.
main source: Wikipedia
A Earth map reconstruction, some 425 mya
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Name: Imidten Formation
Creator: AlDodo
Time period: 425-420 mya
Location: Baltica (Northwestern Eurasia), Scandinavia, (Metropolitan) Denmark, North Jutland, Læsø island
The Silurian, following the end of the Ordovician around 443 mya, and after the Ice Age period defining the latest part of the latter period, which resulted in the Ordovician–Silurian extinction events, causing up to 60% of marine life being wiped out, might be superficially seen as a period of relative stability compared to most other previous and future periods. However, we often observe different important climatic switches within its differents parts, being more unstable and changing at a higher degree.
As a whole, this period is predominantly notable for being comparatively short in geologic terms, being the third and shortest period of the Paleozoic Era, but still a very significant and important one, nonetheless, for Earth’s life as a whole.
It acts as a period of recovery for life and of transition from the Ordovician to the Devonian, both climatically and geology.
For the most part, the Silurian was marked by Earth entering a warm greenhouse period, particulary defined and supported by high CO2 levels of 4500 ppm as well as warm shallow seas which covered much of the equatorial land masses. The climate was dominated by violent storms generated by warm sea surfaces.
With the global temperatures increasing again since the late Ordovican, in which they only slowly continued to fall step by step, the glaciers created by the Ordovician’s ice ige as an effect retreated back into the south polar areas and continued to decrease to even almost disappearing by the middle of the Silurian.
While life does thrive usually better in warm contexts, it still must be said however that the warming climate, which ended the massive ice age period which itself ended the Ordovician and started the Silurian, initially also prolongued the mass extinction and cementing the boundary between the two periods, as the organisms which initially survived the increasing intense cold climate and temperatures, surviving under these conditions, suddenly have to deal with warmer temperatures.
But the warming period of the Silurian was nonetheless quickly favorable for life as a whole, and with rising sea levels, especially during the first half of the period, the shallow waters which mostly disappeared in the Ordovician, due to the cooling climate of the ice age, reappeared and allowed opportunities for many clades. Which radiated and recovered their diversity and population from the losses at the end of the Ordovician.
And while the global climate underwent many drastic fluctuations in temperatures throughout the era, going back and forth between warm and cold, it was never as low as the extreme cold of the late Ordovician nor as high as the extreme heat of the following Devonian.
This would result on minor extinctions occuring within the period, such as around 434 mya, with the start of a global cooling period event making a huge drop in deep ocean oxygen levels, particulary affecting deep ocean life (conodonts, trilobites and graptolites).
At about 428 mya, the start of another oxygen drop led to the extinction of 95% of graptolites.
One, at 424 mya, occured seemingly due to a global drop of sea level as a result of glacier formation. These extinctions were however affecting life more at a local level than at a global level for the most part.
It is only near the end of the Silurian that the climate, which would have remained relatively "stable" for the last almost 25 my, would swift from decently warm to hot temperatures. Creating a new boundary starting the Devonian.
The Silurian is usually viewed by several palaeontologists as an extended recovery interval following the late Ordovician mass extinction (LOME), which interrupted the cascading increase in biodiversity that had continuously been going on throughout the Cambrian and most of the Ordovician.
While the Silurian itself was a rather short period, it still, like the other periods, witnessed other important grades in the evolution of life, not just one but two.
While the Precambrian was marked by the appearance of life, the Cambrian the appearance of derived and recognizable trophic levels and food chains, with the earliest recognizable modern predator and prey dynamics, and the Ordovician the complexification of the ecosystems, the Silurian sees the appearance of the first fully jawed vertebrates, aka the first jawed fish, which would mark the appearance of what is recognizeable as a typical fish by people, and starting the vertebrate line which would lead to one of the most successfull organism lineages that woud dominate Earth for most of the rest of its history.
The clade in question, in which the major evolutionary innovator of the jaws' trait is the Gnathostomata (familiarily refered as "jawed fish"), sitting next to members of the paraphyletic clade Agnatha (refered as "jawless fish", and represented today only by the extant lampreys and kin, and divided into two major morphs, the armored jawless fish and the non-armored jawless fish) from which it is derived (having seemingly evolved from representatives of the armored jawless fish morphs), appeared at the very start of the Silurian, over 439 mya.
The revolution of the movable jaws is as a consensus believed to have evolved from, as surprising as it may sound, from one of the gills that fish have, with the said jaws evolving from the first and closer to the mouth gill arch.
Subsequently it became connected to the skull, giving rise to the typical jaws of most vertebrates, with the following teeth and jaw muscles coming along with it in addition.
The Gnathostomata, perhaps incorrectly refered as the "true fish" ("true fish" evolved by the early-mid Cambrian) initially started with the famous "placoderms" (Placodermi), aka the armored jawed fish, before evolving overtime from this stock into 2 major groups leading to:
the cartilaginous fish (or Chondrichthyes), whose skeleton is made of flexible cartilage (that is often poorly fossilized and preserved), which are thought to have derived from a paraphyletic clade named the acanthodians (Acanthodii) and to which belong the modern extant chimaeras, rays and sharks
and the bony fish (or Osteichthyes), whose skeleton is usually made of bone and in which belong all other modern jawed vertebrates (all modern non-agnathan and non-cartilaginous fish, and includes all tetrapods).
And it is also during this period that the bony fish divided into two groups that would eventually lead to: the modern ray-finned fish and the lobe-finned fish. The latter line would be the one from which later tetrapods will descend from.
And while it was an age of fish radiation and diversification, such as Guiyu oneiros, one of the earliest known fossil member of the lobe-finned fish lineage known, being around 30 centimeters long, or Megamastax at around 1 meter long (among the largest vertebrates on Earth during that time), fish would still remain relatively small, and only reach larger sizes and their peak in diversity during the Devonian.
But the Silurian is even more remembered for another, more important, aspect regarding life’s evolution on Earth, which took place during this period.
This being none others than appearance of the earliest major land animal communities, out of the water.
This major establishment of terrestrial life, no doubt one of the major steps in life’s history, is known as the Silurian-Devonian Terrestrial Revolution.
With plants and fungi further expanding themselves and diversifying, at least three major groups of arthropods (myriapods, arachnids and hexapods) were independently full terrestrial influences, near the end of the period.
Already forming decently complex ecosystems (being the earliest major verifiable soil ecoystem blueprints, persisting for quite a long time), with predatory invertebrates and non-predatory prey animals showing simple food webs in place, also including what seemed to already be detritivores and grazers as well.
The herbivores would be feeding on the simple plant cast composed mostly of representatives of the moss lineage, as well as a few other "tall" plants, and fungi.
Plants and fungi are the initial macrorganisms to have established out of the water and settle on land, with them starting to, overtime, make the terrestrial atmosphere even more breathable, helping create oxygen from CO₂, and as an effect allowing animals to live on land. Arthropods came much before vertebrates, thanks to their lungs which, while more primitve and less sophisticated, were still able to catch the minimal air oxygen level present in the atmosphere at that time.
Despite this remarkable step forward for life, most of its diversity was still predominantly by a extreme margin still living underwater and thriving at a higher level in the seas. Organisms were becoming more diverse and complex than before.
New types of corals arrived (including lineages of tabulate corals, from orders of the Tabulata class) and new crinoids, exploding in diversity.
Brachiopods became abundant and diverse, with the taxonomic composition, ecology, and biodiversity of Silurian brachiopods mirroring Ordovician ones, in good part due to developing, again, high endemism in various parts of the world, and after the LOME event developed novel adaptations for environmental stress. Some of twhe most abundant groups were the atrypidans and pentameridans.
Other successful groups witnessed recovery and major degrees of diversity included the bryozoans, exhibiting particulary significant degrees of endemism to particular shelfs, as well as also developing symbiotic relationships with cnidarians and stromatolites, and the bivalves, including deep sea lineages, while other groups of marine animals such as members of the chiton lineage, hederelloids and tentaculites saw, at that time, a peak of diversity.
Trilobites, in their own side, continued to enjoy success in the Silurian, as they had in the Ordovician, after ecovering from the LOME at the end of the last period, but still, they're now more reduced in clade diversity due to that event.
Some groups, however, faced a decrease in biodiversity and number around that time, such as a sharp decline of jawless fish such as conodonts and "ostracoderms", that could correlate with the diversification and increase of jawed fish. Jawed fish potentially were outcompeting their jawless counterparts due to their novel jaws, allowing them to better consume resources in their environnement, being able to explore more niches.
Members of the cephalopod lineage, the "orthocones", which were, for the most part, dominant invertebrate clades in the Ordovician, were hit hard by the end of said period, but survived and recovered in the Silurian, but would still be on a lesser diversity and would overtime, by the late Silurian, and within the Devonian, decline, step by step, while the jawed fishe would increase in size, number, diversity and population. The fish would be able to use their jaws to break the shells of these cephalopod lineage members.
All to say that this period of Earth’s history was equally, if not more, important than the other periods about the evolution of life on the planet, even so, however, it is relatively less studied, despite putting the very bases and seeds which would one day lead to the land cast of organisms that would end up dominating the planet in the following periods.
Althought the earliest records of animal life in true first major ecosystems on land are recorded from this period, actually very little is known regarding life on land at this point in time, as the number of good and informative formations of such biota are few and far between.
Some of the available ones are of dubious, undertermined dates, such as the Cowie Formation in Scotland, United Kingdom, which dates from the middle Silurian at 430–428 mya to the early Devonian.
However, one novel Silurian formation, not found in our timeline, seemingly offers an additional source of data that may help to better understand furthermore some aspects of how life was on land and filling some gaps in our understanding of Earth’s life in this period.
Present in a very spot on and inhabited area in the middle of human civilization, it remained undiscovered for a very long time to the nearby inhabitants, oblivious to it, while in front of them, being the Imidten Formation.
Found on the small and very isolated island of Læsø, in the territory of Denmark, in North Jutland area, and named in the local tongue from the words i midten, meaning at center in Danish (as the formation is at the very center of the island, inland).
The Imidten Formation is a formation which, compared to the other ones found in our timeline, was difficult to access or hard to spot.
The island of Læsø is not very highly populated, with only a demographic population less than 1,800-1,900 inhabitants (around our timeline's 2020’s), being a very small island and a place that is not particularly heard of (despite a pretty decent level of tourism), but also that just no major paleontological surveys and studies for potential formations are usually conducted. Only a few acheological patrols are made regarding local human populations and related settlements, tools and objects of antiquity, in the last century, for the most part.
Data of the formation is relatively limited, being rather small, only spanning some kilometers (the size of 2-3 small fields), but still offers a very surprising condensed and compacted number of well-preserved fossils and data from the geological rocks.
The rock elements allow the formation's date to be precisely determined to the late middle Silurian and almost the entire late Silurian, around 425-420, spanning the second half of the Ludlow epoch (Ludfordian) and most of the late Silurian (Přídolí). It ends roughly one million year before the end of the Silurian. Some data may suggest the formation potentially may have had a longer lifespan, existing for some additional million years and through the first 2 to 3 million years of the Devonian, but as of now, this idea is conjectural.
Back then, the formation was located somewhere near northern areas of what was once the continent of Baltica, which represent today most of northwestern Eurasia, including Scandinavia and subsequently Denmark.
For the most part, the Imidten Formation was revealed to have been relatively similar, if not identical in broad strokes, to the landscapes on land of other Silurian formations, giving a glance of life out of water already at display.
With the formation itself determined as composed of both land and underwater settings, relatively close to the sea, it’s isn’t known for certain if the exact location was set directly on the coasts or inland, with the sea out of view, instead with important water systems composed of saltwater going pretty far in the interior of the landmass.
The overall landscape of the formation is typical for terrestrial biota at that time, being mostly a flat region (mountains in thr lands on almost all continents were low in number back then), not very high above sea level, and composed of various brackish inland estuarine systems of shallow deltas and rivers of variable sizes scattered within the region. This created many island areas of equally variable sizes.
Most plants remained close to freshwater and brackish ponds, and areas in which both types meet each other and mix.
Almost the entirety of the landscape was otherwise recovered as just a "rug" of members of the moss lineage and several fungi, here and there, forming an entire green ground spanning to infinity and beyond on all the landmass.
These representatives of the moss lineage, and few other plants, with stems directed to the sky by only a few centimeters high, were, as everywhere else back then, part of the earliest major "plains" and "forests" to exist, with various very small arthropods inhabiting this ecosystem.
Most of these found so far, by a wide margin, are millipedes (recognizable typical millipedes, accompanied also by centipedes) and trigonotarbid arachnids. But other arthropods have been found, such as members of the true scorpion lineage, with some representatives of the family Dolichophoniidae, including what seem to be the genus Dilochophonus itself or a similarily closely related genus.
Surprisingly, remains of several thylacocephalan and pycnogonidan (aka sea spiders) have also been found, but it is uncertain, especially for the second group, if these findings represent freshwater species or specimens lost or rejected from the nearby sea into the inland ecosystem of the formation (much more likely for the sea spiders). What appears to be potentially some early hexapods of uncertain affinities have also been recovered from there too.
Additionnaly, what appear to represent an arthropod of an yet undescribed species closely related to the egnimatic genus Parioscorpio of the late early Silurian of the Waukesha Biota (438-433 mya), part of the larger Brandon Bridge Formation, has been uncovered there. If indeed a related animal to it, would not only reveal a new lineage of arthropod in the region but also considerably extend the lifespan of the lineage to almost the entire Silurian period itself. A family suggested for these animals would be named Parioscorpionidae.
The rivers and deltas themselves were more typical underwater ecosystems, forming pretty regular brackish swamps, with mostly animals adapted to saline conditions and many coming from nearby sea being found. Found would be either annual coastal residents or occasional seasonal marine migrants.
"Agnathan" jawless fish are well-represented, with several species of anaspids, few armored osteostracans and 3 traquairaspidiforms, but most fish are represented by acanthodiians, with around up to 16 species known so far.
Besides these, not a lot is known about this formation.
What follows are several well-known organisms from the formation.
Name: Prototaxites laeso
Size: Around 8 meters tall on average
Clade: Fungi, Eumycota, Amastigomycota, Symbiomycota, Dikarya, Ascomycota, Prototaxitaceae, Prototaxites
Prototaxites laeso ("Laeso’s first conifer") is a titanic fungi found in very high abundance in the Imidten Formation and the largest and tallest organism recorded from there. The genus itself is known from a very wide distribution, especially in North America while this specific species so far is only known from this formation in Europe. Its named from the island on which the location is present.
A terrestrial fungi of impressive sizes, it belongs to the Ascomycota, as it is strongly thought as an early member of the Prototaxitaceae family, making it a species of ascomycetes or, more commonly known, a sac fungi. Ascomycetes includes none other than the biggest and most diverse group of the mushroom-bearing lineage of fungi on Earth today.
While several ecologies (also uncertain) have been proposed, there is some consensus that this mushroom fed on a range of substrates, instead of performing photosynthesis, feeding on the remains of whatever other organisms were nearby.
More precisely, it was a fungal rhizomorph, possessing mycelial cords as root-like structures, living by being saprotrophic like many modern fungi.
This is supported and consistent with the fact that Prototaxistes, for all its species, including P. laeso, needed, obviously, a high level of biomass to sustain its body.
At a size of already around 8 meters tall, like for most of the other species of the genus recorded, (variations in sizes exist depending on specimens and populations), this organism was none other than the first (recorded from the fossils record) large land lifeform, largest, longest and tallest (non-animal) organism that existed on Earth’s history, since the appearance of life itself and of its own time. It dwarves all others known Silurian organisms, be them other fungi, plants and animals of both land and sea.
Plants, such as the contemporary Cooksonia (present at the Idmiten Formation), were among the terrestrial lifeforms to arrive in second position in term of size after the giant mushroom, being only around 15-20 centimeters (6-8 inches) tall, to 30 centimeters (12 inches) tall maximum, in comparison.
This makes Prototaxistes laeso, like the rest of the genus as a whole, the ruler and dominant species within its ecosystem. They stood as the "moss-like forests" grew beneath it, in its shadow, while invertebrates were the only other major moving land-dwelling multi-cellular life.
Name: Apuprimiumcutio terrestris
Size: Around 12 centimeters long on average
Clade: Arthropoda, Deuteropoda, Euarthropoda, Antennulata, Mandibulata, Pan-Myriapoda, Euthycarcinoidea, Myriapoda, Progoneata, Diplopoda
Apuprimiumcutio ("among first millipede") is a small archaic millipede of uncertain taxonomic placements living on land, above water, and found so far strictly only in the Imidten Formation and known from around a dozen specimens found at 3 locations within the formation. Its among the earliest and largest "megafaunal" creatures of both this formation and of the world back at the age of the latest Silurian.
A diplopod myriapod, it is a species of multi-legged arthropod which seems to be a moderate presence within the ecosystem’s cast of the terretrial parts of the formation, but still among the largest creatures found on land at the time and seemingly was within the dominant non-predatory creatures within the trophic level. As such, it played an important role in maintaining the local ecosystem, much like the other present arthropods, them too forming what was one of the earliest complex terrestrial food chains to have evolved.
Apuprimiumcutio is a large land animal by the standards of this era, with a lenght of around 12 centimeters and 11 segments both composed of a small paranota (keels) high on the body alogn with long and slender legs. It had 2 pairs of legs for each segments, for a total of 22 legs. The dorsal portion of each segment is ornamented with a horizontal bar and some rows of roughly hexagonal bosses.
The species have its cuticle containing openings which are spiracles, and so part of a gas exchange system that would only work in air, providing evidences that this animal was indeed well a fully terrestrial creature.
Because Apuprimiumcutio is recorded from undoubtable dates earlier than the other millipede Pneumodesmus of uncertain occurrence (due to the formation from which it was recovered, the Cowie Formation, being of debatable geological date, either the Silurian or Devonian), this makes Apuprimiumcutio the earliest documented arthropod with a tracheal system, and among the earliest known oxygen-breathing animals on land. This is, at least compared to the ones we do have definitive dates of occurrence.
Apuprimiumcutio is believed to be an herbivorous animal, and among the main large herbivores of its ecosystems, as indicated by its notably large and robust mandibles. These are thought to serve to cut, process and help to ingest particulary tough and robust vegetal matters.
Thus, the inclination of the head towards the ground seems to suggest this species only eats what is directly growing on and from the ground, meaning its diet includes predominantly members of the moss lineage found in extreme abundance. This would be instead of stems of others plants or the growing layers of mushrooms. This would make Apuprimiumcutio, if true, among the earliest terrestrial "grazing" species to have evolved on Earth.
It is not known if Apuprimiumcutio had a good vision or if it is rather poor or blind, nor if it was diurnal or nocturnal, but its antennae seem to have served an equal role in helping the arthropod move around in its habitat and sense obstacles, predators and congeners.
Name: Dupliciculmus tamisium
Size: Around 15 centimeters long on average
Clade: Arthropoda, Deuteropoda, Euarthropoda, Antennulata, Artiopoda, Trilobitomorpha, Trilobita, Phacopida, Phacopina, Dalmanitoidea, Dalmanitidae, Dalmanitinae, Dalmanitini, Dupliciculmisina
Dupliciculmus ("double stalk") is an unusual species of trilobite recovered from the Imidten Formation, known from plenty of specimens primarily found in what would be areas of mostly freshwater rivers rather than the more saline, brackish parts thought to have logically been closer to the sea.
A dalmanitoid phacopidan, and belonging to the suborder Phacopina, this animal is among the oddest creatures reported from the formation, as it is an unexpected species of this famous group of arthropods in such a context, as trilobites aren’t known to have frequented, even occassionally, freshwater biota in inland regions. This makes it a very remarkable and unique genus within this whole class of extinct Paleozoic creatures. This makes it the first ever undoubted freshwater trilobite ever discovered to date.
Dupliciculmus has been found to be a close relative of the genus Dalmanites, a well-known genus which lived during all the Silurian period, and had a very similar bodyplan.
As a whole, it had a moderately vaulted, slightly convex exoskeleton with a broddly inverted egg-shaped outline, a head shield (or cephalon) which is semicircular, and its limbs are very analogous to the ones of Dalmanites.
However, it differed from this genus in some key aspects. Notably by having the frontal margin of the cephalon diagnosed with several protrusion structures extending the cephalon forward, with 4 pairs in total, and with the first pair being considerably larger than the 3 others.
Meanwhile, the front margin of the cephalon of Dalmanites is semicircular to parabolic, and it may have a simple and short anterior extension.
Given this trait has been found in both in males and females in Dupliciculmus, it is unlikely this would have been a sexual display structure, used for sexual purposes, such as fighting other male opponents over females; such have ben recorded in several families of Phacopidans such as the Acastidae (with Walliserops) in the Acastoidea. In these, males had specialized extension structures in their head to fight each other, so to reverse their opponents on their back.
These would not be used for intimidating other males nor impress females.
Instead, scientists currently think these structures may have served likely for digging and shift sand, soil and substrate underwater, when foraging for food. This makes it a convergent feature but used for entirely different purposes.
Because of these different divergent traits, its concluded, as a consensus, that the Imidten’s trilobite was different enough and having enough diagnostics traits from other related trilobites to be safely assigned to a different genus from Dalmanites and kin, of the Dalmanitidae, but perhaps also within an entirely different family within the Dalmanitoidea group.
This leads to the proposed erection of the family Dupliciculmisidae, to which Dupliciculmus is so far the sole member.
This would make it the fourth family known of this group, after the type family of the Dalmanitoidea, the Diaphanometopidae and the Prosopiscidae.
Name: Aliusalesnumus primus
Size: Around 75-80 centimeters long on average
Clade: Arthropoda, Deuteropoda, Euarthropoda, Arachnomorpha, Chelicerata, Euchelicerata, Prosomapoda, Planaterga, Dekatriata, Sclerophorata, Eurypterida, Eurypterina, Diploperculata, Pterygotioidea, Pterygotidae
Aliusalesnumus ("another winged one") is a decently large predatory aquatic arthropod inhabiting the rivers and shallow lakes and deltas scattered within the Imidten Formation, and whose remains are found in an appreciable number, yet not in a high population. An entire agglomeration of around 30 or so specimens is known, thought to represent a regrouping of female individuals while spawning eventually going deceased, condensed and superimposed on each other. Some other specimens of varying sizes, representing several stages of growth, are found independently.
A pterygotid pterygotioidean eurypterid, this animal, from its type and sole known species, A. primus, named in reference to be among the first organisms known from the Imidten Formation, is a member of the famous arthropod group popularily known as sea scorpions. Its a rather typical member of this group regarding its general bodyplan, being the one people think of when having in mind these animals of this clade.
If Aliusalesnumus, as a sea scorpion, isn’t notable bodyplan-wise, it is, however, on the other hand, sufficiently remarkable for being found in a non-marine setting, which was composed of a decent percentage of freshwater constitution. Various areas of the Imidten Formation weren’t brackish nor were mixed together with freshwater all the time.
This might be seen as unusual for eurypterines, where many prefered a marginal marine and saline setting.
The reason for the presence of such a member of the group isn’t known, so it might be due to potential intense competition in the oceanic setting, given sea scorpions were, at the time, at the peak of their golden age.
But what is sure is that this genus was a year-round resident to the formation, not composed of migrating specimens that momentarily came to a more shallow, shore-like biome to lay their eggs, in which young would live their early years, which is what the find of numerous deceased female specimens found together would have initially made one believe. If that were the case, only females and young with a few years old, would have been recovered, but many males and specimens of various stages of growth have been found as well.
In the ecosystem of the formation, Aliusalesnumus is strongly believed to be an ambush predator, instead of an active pursuit predator, much like most other sea scorpions.
This sea scorpion is even justly extremely remarkable for a trait supporting such lifestyle, not seen anywhere else in the entire group, and something to do with its specialized chelicerae converted into claws similar to the ones of scorpions or crustacean, in which they are unique in that they are built specifically for retaining and keeping prey rather than grasping.
The "teeth" of the claws act as spikes on both the "hand" and "finger", being disposed in a way that the spikes of one side fit in the holes between two of the spikes of the other side. The spikes of the "hand" and the spikes of the "finger" interlock and fit perfectly when the pliers are completely closed.
Ending with an efficient tool to retain prey, with the spikes of both sides sinking into the flesh of the target, in two different areas, the victim is unable to easily free itself, as attempting to swim in either direction leads to one row of spikes sinking deeper into the flesh even more by doing so.
Because of this, it is believed that the genus had a diet of predominantly small soft-bodied prey, which are thought to have been mainly unarmored jawless and jawed fish, as its claws aren’t strong enough to deal with hard or armored species, and its spike-like structures served to retain prey would break under a too high stress or effort.
Name: Asadrepanopterus longumfinus
Size: Around 60 centimeters long on average
Clade: Arthropoda, Deuteropoda, Euarthropoda, Arachnomorpha, Chelicerata, Euchelicerata, Prosomapoda, Planaterga, Dekatriata, Sclerophorata, Eurypterida, Stylonurina, Mycteropoidea, Drepanopteridae
Asadrepanopterus ("like-Drepanopterus") is another, relatively common sea scorpion compared to Aliusalesnumus, and of similar sizes, albeit slightly smaller in average than the latter, found in various parts of the Imidten Formation, in deposits offering better conditions for fossilization processes. A female specimen is preserved with a clutch of eggs found inside her body and thought to be about to be layed.
A drepanopterid mycteropoid, this genus, composed by its only known species, A. longumfinus, is one of the 3 stylonurine sea scorpions found within the formation, making a total of 4 sea scorpions as a whole, with Aliusalesnumus if eurypterines are included, and the one which is the most abundant with all the members of both groups recorded from the formation.
It possesses a broad, rounded head carapace, with its abdomen rather surprisingly thin, with the transition from the broad form to the thin, slender rear being rather drastic at a given point in the body. The telson at the end of the abdomen is also notably elongated compared to most other stylonurines, forming a sort of spear-like structure in some perspectives. The type species of this genus has been named based on this trait with longumfinus meaning "long fin".
This animal also possesses lateral compound eyes with parallel axes on a subrectangular to subovate prosoma (head). With the first three pairs of legs, appendages I (not visible in a view from above such as in the picture provided here), II and III being short and powerful, with spines. The following three pairs are moderately long, with each ending in a strongly curved terminal claw. The last leg of the three reaches as far as the penultimate abdominal segment (not including the telson).
Because of the disposition and size of its legs, as well as the fact its a rather heavily built animal, Asadrepanopterus isn’t a fast nor agile arthropod, and instead a pretty slow-moving creature.
Its locomotion is well-known thanks to numerous fossilized trackways found in the formation, attributed to this genus.
These fossilized eurypterid trackways tend to be large and heteropodous, often having the associated telson dragging mark along the mid-line and leavign a clear line between two rows of rounded spots on the ground. The trackways of this species are indeed formed as such.
It is accepted, as a consensus, that this animal is a slow predator and detritivorous scavenger, and only eats very small to near microscopic prey (mainly fauna and maybe alongside a small part of plant matter, accidentably, reminding one of the bonnethead shark, Sphyrna tiburo), fitting a niche akin to horseshoes crabs, and being more precisely a sweep-feeder (raking through the substrate in search of prey).
Name: Sawdonia abundans
Size: Around 8-9 centimeters long on average
Clade: Plantae, Charophyta, Phragmoplastophyta, Embryophytes, Polysporangiophytes, Tracheophyta, Eutracheophytes, Lycophytina, Zosterophyta, Zosterophyllophytina, Zosterophyllopsida, Zosterophylls, Sawdoniales, Sawdoniaceae, Sawdonia
Sawdonia abundans ("abundant Sawdonia") is a widespread and dominant species of early vascular plants known from the Imidten Formation, with most fossils being recovered from areas which were near water ponds, and from which its density of population is the most abundant. Hence its species’ name.
A member of the zosterophylls in the order Sawdoniales, to which its genus is the type from which this group is named, belongs to Sawdonia, which has an almost cosmopolitan distribution across the globe. It is found in an extremely broad range of countries, from Canada in North America (at the Battery Point Formation), Venezuela (at the Campo Chico Formation) in South America, as well as in England and Scotland in Europe (at the Strathmore Group). Some possible still undefined records exist from China, in Asia.
The species found in the Imidten Formation, S. abundans, represents one of the easrliest occurrences of this genus.
Sawdonia abundans is overall pretty analogous to the other known species of this plant, best recognized by the large number of spikes/spines (enations) covering it, clearly visible along the leafless green photosynthetic stem they grow on. But despite being a vascular plant, there aren't vascular systems in said enations. These are tapered and pointed lower on the plant but form loose spikes at end of the plant.
The stems of the plant are monopodially branched, being unridged, spinous and circinately tipped, bearing sporangia which are round in an abaxial view and oval in a lateral view. These same sporangia are formed laterally and singular on short stalks.
Another traits of the plant being the xylem being simple as displayed as one solid strand, while the epidermal cells have cuticular papillae and stomata being present on the stem but not on spine surfaces.
In this specific species, S. abundans, the stems grow at the ends by unrolling themselves, a process known as circinate vernation.
To be added
Milne Bay Formation / Papua New Guinea (430 mya) - Not all of the Cambrian fauna died out after the period’s end. In fact many are still around as of the Silurian. Some have even managed to reach the fringes of the land, just a few steps away from becoming terrestrial. However, almost none will achieve this, whether because of diet, breathing methods or competition. Nevertheless, the Milne Bay Formation gives us an insight as to what intertidal life looked like in the shallows of Silurian Gondwana, alongside some interesting precursors to the life of the Devonian. (IC1101)
Imidten Formation / Baltica (Northwestern Eurasia), Scandinavia, (Metropolitan) Denmark, North Jutland, Læsø island (425-420 mya) - One novel Silurian formation, not found in our timeline, seemingly offers an additional source of data that may help to better understand furthermore some aspects of how life was on land and filling some gaps in our understanding of Earth’s life in this period. Present in a very spot on and inhabited area in the middle of human civilization, it remained undiscovered for a very long time to the nearby inhabitants, oblivious to it, while in front of them, being the Imidten Formation. Found on the small and very isolated island of Læsø, in the territory of Denmark, in North Jutland area, and named in the local tongue from the words i midten, meaning at center in Danish (as the formation is at the very center of the island, inland). The Imidten Formation is a formation which, compared to the other ones found in our timeline, was difficult to access or hard to spot. The island of Læsø is not very highly populated, with only a demographic population less than 1,800-1,900 inhabitants (around our timeline's 2020’s), being a very small island and a place that is not particularly heard of (despite a pretty decent level of tourism), but also that just no major paleontological surveys and studies for potential formations are usually conducted. Only a few acheological patrols are made regarding local human populations and related settlements, tools and objects of antiquity, in the last century, for the most part. Data of the formation is relatively limited, being rather small, only spanning some kilometers (the size of 2-3 small fields), but still offers a very surprising condensed and compacted number of well-preserved fossils and data from the geological rocks. The rock elements allow the formation's date to be precisely determined to the late middle Silurian and almost the entire late Silurian, around 425-420, spanning the second half of the Ludlow epoch (Ludfordian) and most of the late Silurian (Přídolí). It ends roughly one million year before the end of the Silurian. Some data may suggest the formation potentially may have had a longer lifespan, existing for some additional million years and through the first 2 to 3 million years of the Devonian, but as of now, this idea is conjectural. Back then, the formation was located somewhere near northern areas of what was once the continent of Baltica, which represent today most of northwestern Eurasia, including Scandinavia and subsequently Denmark. For the most part, the Imidten Formation was revealed to have been relatively similar, if not identical in broad strokes, to the landscapes on land of other Silurian formations, giving a glance of life out of water already at display. With the formation itself determined as composed of both land and underwater settings, relatively close to the sea, it’s isn’t known for certain if the exact location was set directly on the coasts or inland, with the sea out of view, instead with important water systems composed of saltwater going pretty far in the interior of the landmass. The overall landscape of the formation is typical for terrestrial biota at that time, being mostly a flat region (mountains in thr lands on almost all continents were low in number back then), not very high above sea level, and composed of various brackish inland estuarine systems of shallow deltas and rivers of variable sizes scattered within the region. This created many island areas of equally variable sizes. Most plants remained close to freshwater and brackish ponds, and areas in which both types meet each other and mix. Almost the entirety of the landscape was otherwise recovered as just a "rug" of members of the moss lineage and several fungi, here and there, forming an entire green ground spanning to infinity and beyond on all the landmass. These representatives of the moss lineage, and few other plants, with stems directed to the sky by only a few centimeters high, were, as everywhere else back then, part of the earliest major "plains" and "forests" to exist, with various very small arthropods inhabiting this ecosystem. Most of these found so far, by a wide margin, are millipedes (recognizable typical millipedes, accompanied also by centipedes) and trigonotarbid arachnids. But other arthropods have been found, such as members of the true scorpion lineage, with some representatives of the family Dolichophoniidae, including what seem to be the genus Dilochophonus itself or a similarily closely related genus. Surprisingly, remains of several thylacocephalan and pycnogonidan (aka sea spiders) have also been found, but it is uncertain, especially for the second group, if these findings represent freshwater species or specimens lost or rejected from the nearby sea into the inland ecosystem of the formation (much more likely for the sea spiders). What appears to be potentially some early hexapods of uncertain affinities have also been recovered from there too. Additionnaly, what appear to represent an arthropod of an yet undescribed species closely related to the egnimatic genus Parioscorpio of the late early Silurian of the Waukesha Biota (438-433 mya), part of the larger Brandon Bridge Formation, has been uncovered there. If indeed a related animal to it, would not only reveal a new lineage of arthropod in the region but also considerably extend the lifespan of the lineage to almost the entire Silurian period itself. A family suggested for these animals would be named Parioscorpionidae. The rivers and deltas themselves were more typical underwater ecosystems, forming pretty regular brackish swamps, with mostly animals adapted to saline conditions and many coming from nearby sea being found. Found would be either annual coastal residents or occasional seasonal marine migrants. "Agnathan" jawless fish are well-represented, with several species of anaspids, few armored osteostracans and 3 traquairaspidiforms, but most fish are represented by acanthodiians, with around up to 16 species known so far. Besides these, not a lot is known about this formation. (AlDodo)
Friendship Formation / Off the coast of Mauritania (421 mya) - Terrestrial life has been establishing across the world in the Silurian, to a level far more complex than in previous periods. While notable fossil formations in Laurentia and Baltica showcase a diverse early terrestrial environment, little is known on how it was manifested in the larger Gondwana continent. Scant evidence exists about the terrestrial life that existed there, with records of a diverse array of plant life, as well as a few signs that arthropods, like myriapods and others, were present. Notably, in Australia, some of the oldest terrestrial arthropod fossil tracks are known, noting how life was already establishing inland perhaps even before the iconic Ludlow and Přídolí terrestrial communities of other continents, even in harsh environments like deserts. However, terrestrial life in Gondwana, during the Silurian, is still vastly unknown. The Friendship Formation is a peculiar ecosystem, dated to the Přídolí epoch, some 421 million years, roughly contemporaneous with the Cowie Formation of Scotland. Unlike the latter, which depicts a nice and warm tropical environment, the Friendship Formation was located on what is today the seaways west to Mauritania, back then part of an ancient landstrip in the Antarctic Circle. After the Lau event, at the end of the Ludlow, global temperatures increased, and old land bridges started to fragment into smaller landways surrounded by sea, increasing endemism in various landmasses. The warmer temperatures also promoted higher biotic diversity and allowed life to thrive even in the polar regions, free of glaciation, during the Přídolí. The Friendship Formation is notable because it shows a variety of incredibly tiny organisms that would never or hardly preserve in any ideal fossil condition, giving us a glimpse on the diversity of Silurian terrestrial ecosystems. (YellowPanda2001)
SPECIES
Name: Bathycaridipodia plumabrachis
Creator: TheTiger773
Size: 30 centimeters long (full body)
Location: Divergent boundaries under the Paleo-Tethys Ocean, west of Gondwana
Time period: 425.6 mya
Clade: Tactopoda, Arthropoda, Deuteropoda, Euarthropoda, Antennulata
Bathycaridipodia plumabrachis is a very unusual species of deep sea arthropods that are members of the Deuteropoda clade. Its name comes from the large feather-like appendages, covered in dense setae, that host dense colonies of bacteria. This is because Bathycaridipodia is a firm resident of active hydrothermal vents, or rather their outskirts. The microorganisms living on setae are chemotrophs, living of the sulfur rich soup constantly spewed from the vents. The same microorganisms in turn are a main food source of this animal. While such case of mutualism is nothing out of ordinary in modern nature, it may be surprising to see it in this environment, especially this far into the past. Another important characteristics are a pale exoskeleton and diminished eyes due to lack of light in its home environment. Because of that, Bathycaridipodia posses a pair of long antennae that they use to probe their environment in order to find possible danger or mates. Females of this species can lay up to 60 eggs, that are held under their body until they hatch. Despite their vague resemblance to mandibulates, their ancestry diverged from them during Cambrian, as their closest relatives are members of Fuxianhuiida clade. However, this makes it part of a well over 80 million year old ghost lineage. It seems like the ancestors of this species must have relatively quickly adapt to deep sea environment, somewhat explaining their absence from the fossil record. Their adaptations to the foraging on the sea floor and near the hydrothermal vents were the main reason they were able to survive this long. However, the increasing competition from similary adapted trilobites eventually caused their extinction during the Pridoli epoch.
ECOSYSTEMS
Name: Zemmour Formation
Creator: YellowPanda2001
Time period: 435 mya
Location: Northeastern Mauritania
The Silurian was a period of immense evolutionary turnovers, with various groups of organisms suffering through explosions of diversity after the Ordovician extinction event. Especially with the retreat of glacial periods, polar regions, once ravaged by thick layers of permanent ice, have since been recolonized again. This is the case of the Zemmour Formation, a region that corresponds to the modern desertic and uninhabited regions of northeastern Mauritania. Back some 435 million years ago, in the early Silurian, in the Telychian age, this region was a shallow polar sea, free of glaciation, where the hothouse conditions allowed for a plethora of organisms to abound here. The Zemmour Formation was home to early representatives of organisms that would become very successful in the following millions of years, showcasing how the traditional Silurian-Devonian fauna was establishing and diversifying, at a global scale, soon after the end Ordovician extinction. This ecosystem would later disappear with the Ireviken glaciations, a few million years later.
Name: Protonothia insularis
Size: 5-15 centimeters tall
Clade: Lycophytes, Protonothiaceae
Although the Zemmour Formation is mostly dominated by marine fauna and flora, it is also known for some terrestrial taxa, hailing from isolated islands and atolls that exist in between the shallow sea. There, early land plants are present in the landscape, including a peculiar species: Protonothia insularis. This is a representative of a specific family, Protonothiaceae, and it is actually a very early diverging lycophyte, the lineage that would give rise to the lycopods. It is at the very base of the lycopod stem-tree, very near the point of divergence between lycopods and euphyllophytes. It resembles the early Devonian genus Nothia, but it is much more basal than it. This coastal island-dwelling plant is abundant and often many of these plants can be seen floating around in the ocean, ravaged from a storm, or a flash flood, where their stems fall on and decompose, forming a great source of nutrients for the ocean life. This species is evidence that land plants were diversifying and evolving much earlier than what the fossil record tells us.
Name: Physeterichthys wilsoni
Size: 20 centimeters long
Clade: Acanthodii, Ishnacanthiformes
Another surprising creature for the early Silurian, are jawed fish. Jawed fish are known from fossils of the early Silurian, but their exact evolutionary background is enigmatic. Physeterichthys wilsoni represents an early Silurian acanthodiian, therefore an early representative of the chondrichthyan lineage. Although acanthodiians are known from earlier fossil strata, this represents the earliest ishnacanthiiform, a group of acanthodiians known for being specialized nektonic predators. Physeterichthys is therefore the most basal of the lineage, but it is peculiar for the presence of a bulbous front end of its upper jaw, giving its head a spermwhale-like appearance, hence its name. This fish transports the ecology and characteristics of its group to a time slightly more ancient than one would initially believe. Its favorite prey are swimming animals that move in the water column, but it can hunt prey near the benthos too.
Name: Arachnostylonurus clypeus
Size: 15 centimeters long
Clade: Stylonuridae, Arachnostylonurinae
The Silurian period was also a prime moment of diversification of eurypterids, specifically the ones of the Stylonurina group. While stylonurinans were present since the Ordovician, it was in the Silurian and Devonian periods, where their major diversification occured. The Zemmour Formation is home to a strange basal stylonurid, that forms its own distinct subfamily, Arachnostylonurinae. This is Arachnostylonurus clypeus, a small eurypterid, the size of a human hand, with two pairs of very long spider-like legs and an incredibly long curved and needle-thin telson at the tip of its tail. The function of the telson is unclear but might have been used for defense against predators, such as Physeterichthys. This eurypterid was, undoubtedly, a small crawling arthropod, moving in the sea bottom with its long spider-like legs. Unlike more derived stylonurids, its frontal appendages weren't adapted for sweep feeding, so this species was most surely a scavenger, feeding on dead material that appeared in the benthos, including even dead fallen stems of Protonothia.
Name: Milne Bay Formation
Creator: IC1101
Time period: 430 mya
Location: Papua New Guinea
The Milne Bay Formation is peculiar for harbouring an array of creatures that are relics from ancient times. Not all of the Cambrian fauna died out after the period’s end. Many are still around in the Silurian. In this formation, some have even managed to reach the fringes of the land, just a few steps away from becoming terrestrial. However, almost none of these relics will achieve this, probably because of dietary or breathing constraints or due to competition. Nevertheless, the Milne Bay Formation gives us an insight as to what intertidal life looked like in the shallows of Silurian Gondwana, alongside some interesting precursors to the life of the Devonian.
Name: Aigialocaris chelaphora
Creator: IC1101
Size: Around 10 centimeters long
Clade: Mandibulata, Pan-Myriapoda, Hymenocarina, Protocarididae
This unusual arthropod is a late-surviving hymenocarine, similar to the likes of “Papiliomaris” from the Waukesha Biota. However, this one is a member of Protocarididae, the “clawed” hymenocarines. This relatively short, squat hymenocarine is closely related to the Cambrian Tokummia, sharing the large claws and multi-segmented trunk with this genus. It’s a nektobenthic (swimming, but mostly near the bottom) predator, feasting on small fish, soft-bodied arthropods and worms. Occasionally, if they smell washed-up prey on the shore, they will crawl out of the water, retrieve a piece, them crawl back in before they dehydrate. The gills of this species are layered with small hardened struts keeping them from clumping up when out of the water.
Name: Desmoxerxes promyrios
Creator: IC1101
Size: Around 25 centimeters long
Clade: Mandibulata, Pan-Myriapoda, Euthycarcinoidea
A longstanding mystery in palaeontology is finally answered with Milne Bay, that being how myriapods evolved from euthycarcinoids. Desmoxerxes provides an answer. Resembling sottyxerxians, centipedes and millipedes in body plan, this relative colossus was likely on the verge of complete terrestriality, with pouches containing primitive lungs on its underbelly ensuring it could breathe on land. Unusually, it was likely omnivorous, with centipede-like mouthparts alongside small eyestalks eerily similar to those of Arthropleura. This suggests that arthropleurideans may actually be basal to the myriapod crown group, although still derived enough to have developed lungs. Desmoxerxes also bears a small, triangular postabdomen, tucked under its last segments like a crab's "apron". Its tergites (the hard plates on its top) were slightly extended out, although not as much as in Arthropleura.
Name: Venatocaris coralliferus
Creator: YellowPanda2001
Size: 5 centimeters long
Clade: Antennulata, Acheronautidae
Venatocaris coralliferus is a strange predator from the shallow reefs of Milne Bay. It is very strange, with a rounded "head", a long curved body that can hold on to sponges, corals and crinoids, and raptorial arms. This is an ambush predator, clinging to any sort of biotic growth in the reef, thanks to its "tail", that allows it to avoid being dragged by the currents. Like a seahorse, it moves slowly and steadily, only to strike at immensely fast speeds using its raptorial arms, catching a swimming prey. This tactic allows this acheronautid to appropriate from prey above the benthos, such as swimming arthropods, small fish, etc.
Name: Milneaspis phycophagus
Creator: IC1101
Size: Around 1.5 centimeters long
Clade: Arthropoda, Deuteropoda, Euarthropoda, Antennulata, Artiopoda, Trilobitomorpha, Conciliterga, Helmetiida, Helmetiidae
The artiopods have also gotten in on the intertidal action, although, due to their reliance on saltwater, none have made the leap to being fully terrestrial yet. This small helmetiid is probably closest, though. This is due to it laying eggs in seaweed, instead of sediment or open water. It also eats the seaweed, similar to modern kelp flies. By staying within algae it keeps itself warm and moist, avoiding the issue of drying up. Milneaspis seems to have had two different kinds of eggs, one being smaller and softer and likely the "normal" egg type, while the other is much harder (indeed, other Silurian formations nearby also preserve fossils similar to it) and likely represents a more resilient egg for times of extreme weather or temperature, much like the cysts of modern fairy shrimp. As for its closest relative, Kuamaia seems a good candidate, as both have relatively small spines and a rounded body. In addition, a peculiar trait of Milneaspis larvae is that no protaspid stage is known, with even larvae found within hatched eggs being late meraspids at the earliest. This seems to suggest that they developed mostly inside the egg, only leaving once they were large enough to survive on land.
Name: Deinocaris syntribos
Creator: IC1101
Size: Around 1.2 meters long
Clade: Arthropoda, Arachnomorpha, Chelicerata, Habeliida, Habeliidae
The terror of this ecosystem is not one of the numerous eurypterids, nor a towering orthocone, nor even a radiodont, like the Cambrian amplectobeluids. No, the apex predator of these waters is far stranger. D. syntribos is closely related to Habelia itself, sharing the five pairs of gnathobases used to crush prey. It is intermediate between Habelia and the sanctacaridids in body shape, resembling a slender, spiny trilobite from above. The gnathobase-bearing appendages have been modified greatly, with their exopods becoming wiry antennae used for sensing vibration, and the endopods resembling the raptorial appendages of megalograptid eurypterids. Deinocaris is quite indiscriminate in its diet, eating any relatively large animals it came across, including even those with hard shells such as trilobites. In fact, one of its favoured prey items is a species of large lichid trilobite. Not even pelagic animals are safe from this predator, as its flap-like exopods on later limbs have grown larger, allowing it to swim quite fast. It is unclear how such a lineage of arthropods remained undetected for so long, since the Cambrian but, like many other relics from the Milne Bay Formation, it is feasible to imagine that these organisms survived as relics in deep sea environments, which remained relatively preserved through the Ordovician. Once the end Ordovician extinction occured, the eccological gap was sufficient to lead some of those deep sea lineages to recolonize the shallows, explaining the large amount of ghost lineages that reappear in the Silurian period.
Name: Milnechaeta aulocephalus
Creator: IC1101
Size: Around 5 centimeters long
Clade: Annelida, Pleistoannelida, Sedentaria, Terebellida, Cirratuliformia, Iotuboidea
Even previously monotypic clades are represented at Milne Bay, such as the "iotuboids", a basal grade of flabelligerid worm relatives. Similar to their modern relatives, Milnechaeta is often detritivorous, feeding on substrate and falling particles with several pairs of tentacles on its head. However, in times of famine, it puts the "cage" its relatives were named for to good use. One pair of the head tentacles has become hardened and spiny to capture prey. When a small animal swims over it, the numerous bristles around its head close in as the head retracts. Then, the worm extends its tentacles to hold the prey in place before swallowing it and grinding it up with hard plates inside its gut. Milnechaeta is mostly sedentary, however it can slowly creep around on the seafloor much like an earthworm through peristalsis, or even swimming for short periods with its parapodia.
Name: Eodendron prospermus
Creator: IC1101
Size: Around 2 meters tall
Clade: Tracheophytes, Eutracheophytes, Euphyllophytes
The second of the great mysteries solved was that of the discrepancy between molecular clocks and fossils for plants. In particular, seed-bearing plants just seem to appear in the mid-Devonian, with only the progymnosperms and a few other fossils linking them to the rest. Not only was Eodendron thought to be near the higher end of the seed plant stem (similar to Runcaria), but it also appeared to extend seed-bearing plants back tens of millions of years (however, a closer look shows that it is placed almost directly near the fern/seed plant split, with more derived traits likely being convergent). Despite this, it looks fairly anticlimactic. Not much more than a small shrub with feathery leaves, a woody trunk and some small seeds in lattice-like structures. Quite ironic how one of the seemingly most important plant fossils in the history of palaeontology would barely be acknowledged by passers-by if it was alive today.
Name: Parataxites australis
Creator: YellowPanda2001
Size: Up to 30 centimeters tall
Clade: CAM, Prototaxitaceae
Parataxites australis is a towering coastal terrestrial organism, related to Prototaxites. For the longest time, it was believed that the group that this species belongs to was a type of fungus. However, it actually belongs to its entirely distinct group of organisms, a lineage of eukaryotes that independently evolved multicellular lifestyles. Although impossible to infer from fossils alone, Parataxites and kin actually belong to a strange lineage of eukaryotes from the CAM lineage, close to archaeplastidan algae, but unlike them, they are not photosynthetic and are instead saprotrophic heterotrophs. Towering above early plant growths, Parataxites can reach up to half a meter in height.
Name: Friendship Formation
Creator: YellowPanda2001
Time period: 421 mya
Location: Off the coast of Mauritania
Terrestrial life has been establishing across the world in the Silurian, to a level far more complex than in previous periods. While notable fossil formations in Laurentia and Baltica showcase a diverse early terrestrial environment, little is known on how it was manifested in the larger Gondwana continent. Scant evidence exists about the terrestrial life that existed there, with records of a diverse array of plant life, as well as a few signs that arthropods, like myriapods and others, were present. Notably, in Australia, some of the oldest terrestrial arthropod fossil tracks are known, noting how life was already establishing inland perhaps even before the iconic Ludlow and Přídolí terrestrial communities of other continents, even in harsh environments like deserts. However, terrestrial life in Gondwana, during the Silurian, is still vastly unknown. The Friendship Formation is a peculiar ecosystem, dated to the Přídolí epoch, some 421 million years, roughly contemporaneous with the Cowie Formation of Scotland. Unlike the latter, which depicts a nice and warm tropical environment, the Friendship Formation was located on what is today the seaways west to Mauritania, back then part of an ancient landstrip in the Antarctic Circle. After the Lau event, at the end of the Ludlow, global temperatures increased, and old land bridges started to fragment into smaller landways surrounded by sea, increasing endemism in various landmasses. The warmer temperatures also promoted higher biotic diversity and allowed life to thrive even in the polar regions, free of glaciation, during the Přídolí. The Friendship Formation is notable because it shows a variety of incredibly tiny organisms that would never or hardly preserve in any ideal fossil condition, giving us a glimpse on the diversity of Silurian terrestrial ecosystems.
Name: Mauvea floralis
Size: Up to 35 centimeters wide
Clade: Myxogastria, Ceratiomycetes, Mauveamycetes
Plants, animals and fungi take the spotlight when one speaks about terrestrial colonizations on land, but in fact a multitude of other organisms have also made landfall. Growing like a fungus in the "mossy" plant undergrowths is a strange yellow slime mold that often grows tiny rose-like fruiting bodies. This is Mauvea floralis, a member of its own class, Mauveamycetes, sister to the extant Ceratiomyxomycetes class. These may look like fungi, but they're actually amoebozoans. Amoebozoan slime molds are very common in our timeline's today, and their origins go very far back, taking part of early multicellular incursions onto land. These slime molds can expand a lot, consuming rotting material. They form colorful fruiting bodies that grow tall (just about a few millimeters) to aid in spreading spores across the polar landscape. But they have the aid of a few more mobile inhabitants of the Friendship Formation.
Name: Zebracarus sporophagus
Size: Up to 3 millimeters long
Clade: Arachnida, Protoacariformes
Incredibly tiny, moving along the tiny leaves and stems of the local plants, is Zebracarus sporophagus, an arachnid arthropod. It is actually part of its own superorder, named Protoacariformes, being actually more related to the extant Parasitiformes, notable for including ticks and kin. Unlike ticks, they're not really parasites. Instead, Zebracarus is an opportunistic detritivore, going after invertebrate carcasses, plant spores, and fungi. It has a fancy taste for slime molds, commonly hunting for Mauvea. However, the fruiting bodies are usually the most appetizing treats of this amoebozoan, with the flaking "petals" being particularly delicious. As the arachnid feeds, however, spores get attached to the arthropod, helping it spread across the landscape, a necessary sacrifice for the slime mold. It is currently unclear how arachnids reached Gondwana. All undoubted Silurian arachnid fossils are found in laurussian lands, and the earliest definitive arachnid fossils in Gondwana appear in the Devonian, when a land bridge between the two landmasses was already present. However, there was undoubtful interchange between Gondwana and the other landmasses, despite a large ocean separating them. Island chains formed around the mid-late Silurian, allowing for the dispersal of specific plant lineages, as well as myriapods, to exist in both sides of the world. Small arachnids must have made the cross, in order to exist in both regions. The existence of Zebracarus in the polar regions of Gondwana is a clear indication that the conditions at the end of the Silurian were optimal for terrestrial life to, essentially, thrive in every single corner of land in the world, giving significance to the terrestrial revolution that was ocurrying around this time.
EXTINCTIONS
Stem-Bacteria (†432.9 mya): - Life has evolved all the way back in the depths of the Precambrian, and, in our timeline's today, are represented by a few major branches of living organisms, being those eukryotes, archaeans (though these might be paraphyletic in respect to eukaryotes) and bacteria. Bacteria are a monophyletic clade that effectively dominates the world by existing in every single ecosystem on Earth. The first bacteria evolved roughly around 3.5 billion years, but more primitive relatives of bacteria persisted from those Precambrian times, undetected, until much later in time. The last of these "stem-bacteria" survived into the early-mid Silurian, as deep sea hyperthermophiles in secluded abyssal regions. These relics of a Precambrian past, however, were restricted to specific and vulnerable environments, and eventually went extinct during the Ireviken event, an extinction event during the early Wenlock that affected deep sea life. There, the last close relatives of bacteria went extinct, leaving crown bacteria to be the sole dominant members of their own lineage. (YellowPanda2001)
Bathycaridipodia clade (†421.1 mya): - Their adaptations to the foraging on the sea floor and near the hydrothermal vents were the main reason they were able to survive this long. Increasing competition from similary adapted trilobites eventually caused their extinction during the Pridoli epoch. (TheTiger773)
Parioscorpionidae (†420 mya): - Parioscorpio is a unique fossil known from the early Silurian Waukesha Biota. It is the only known fossil representative of its lineage, which one could name it Parioscorpionidae. Its classification is disputed, but it seems probable that it represents a unique lineage of basal stem-mandibulate, closer to mandibulates proper than to artiopods (trilobites and kin). However, representatives of parioscorpionids did survive up until the late Silurian, some 420 million years ago, in the Přídolí epoch. These were late surviving stragglers from earlier epochs, and went extinct quietly with faunal turnovers occurying at the Silurian-Devonian transition. (YellowPanda2001)
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