By the late Cimexian Epoch, roughly 30 million years after the first scuttlebug was born, Atmos’s terrestrial ecosystems had been radically transformed. In the absence of terrestrial predators and any competition whatsoever, the scuttlebugs radiated into an array of forms. Though constrained in size by their hydrostatic physiology and semi-rigid exoskeletons, scuttlebugs became the dominant mobile organisms on land, expanding across Atmos with great success.
From the shorelines of Sorlona, to the humid lowlands of Weslona, and the temperate valleys of Eslona, scuttlebugs colonized nearly every biome available to them. Some scurried through terraspore mats feeding on fungal growths, others clambered up cyanophyte stems in search of spores or shelter, and many adapted to leaf litter, roots, or crevices in the soil. Their small size proved to be an advantage in these early ecosystems, allowing them to exploit microhabitats and avoid desiccation in the still-developing terrestrial atmosphere.
Sentirecimexes (Feeling Bugs) represents one of the most ecologically successful early clades of scuttlebugs to emerge during the mid-Cimexian Epoch. Distinguished by their sensory appendages, these creatures evolved to thrive in environments rich in decaying organic matter, fungal mats, and detritus-heavy forest floors. While they remained small, ranging from a few millimeters to a few centimeters in length, their intricate behaviors, specialized limbs, and diverse feeding strategies placed them among the most prevalent of the early terrestrial fauna on Atmos.
The most defining feature of the sentirecimexes is the transformation of their upper limbs into elongated, flexible, tactile antennae positioned adjacent to the mouth. These whip-like structures are covered in sensitive chemo- and mechanoreceptors, allowing them to “feel” their way through dark or cluttered environments with precision. Rather than relying on visual cues, most species used these limbs to map their surroundings, taste the air, and detect fungal growths or decaying matter from several centimeters away.
Their forward thorax also became more rigid, providing support for their muscular grasping limbs just below the antennae, which were used to manipulate food, climb, or sweep aside debris. Their body tapered into a segmented trunk with dense arrays of stubby walking limbs, giving them a caterpillar-like scuttle across terrain.
Many species of sentirecimexes could be found across Atmos's southern continents during the Cimexian. Sentirecimex muscocursor was a fast-moving litter-skimmer. This species occupied the damp microclimates between thick patches of terraspore leaf bases. Its antennae were constantly in motion, sweeping across surfaces as it darted in zigzag patterns to avoid predators and locate nutrient-rich detritus. Muscocursor fed primarily on decaying terraspore strands and moist rot, using its sensitive taste-pits to distinguish between viable and toxic substrates.
Sentirecimex stipifex was a larger, slower-moving browser. Stipifex clung to the stalks of early terraspores, climbing into low fungal groves to feed on the soft, nutrient-rich undersides of their spore sacs. Its footpads were adapted for vertical gripping, and it possessed reinforced mandibles for slicing into soft tissues. This species often cohabited with certain microsporulating terraspores, acting as a passive spore disperser.
Sentirecimex pulsopectus, or "Drummer Bugs,” were unique among the sentirecimexes, in that this species communicated using rhythmic drumming of its legs against hollow terraspore stalks, so as to ward off rivals or attract mates. Found in shaded groves on southern Weslona, pulsopectus lived in loose aggregations, each individual drumming a slightly different signature beat, a primitive form of acoustic niche partitioning.
Scandicimexis (Climbing Bugs) was an an agile and highly specialized offshoot of the broader scuttlebug lineage that arose during the latter half of the Cimexian Epoch. As trunk microclimbers, scandicimexes represented one of the first terrestrial animal groups on Atmos to adapt fully to life in the vertical strata of dendriradix forests, living among the tangled aerial root systems of the blue trees. Scandicimexes were easily recognized by their hooked, grasping feet, which allowed them to cling tightly to uneven surfaces like bark mats, porous root walls, and fibrous terraspore stalks. Their posterior walking limbs were arranged in alternating pairs and were stiffened for stability, while the front limbs shifted upward to the mid-chest region, forming a secondary set of powerful, articulated climbing arms. These were used like grappling tools to pull themselves across vertical and even inverted surfaces.
Another key adaptation was their elongated, flexible lips, which acted like soft proboscises. These lips could wrap around porous surfaces and shallow crevices, drawing out moisture, microbial film, or terraspore exudates. The lips were lined with fine cilia and enzyme-secreting cells that helped dissolve organic matter for ingestion. Despite their somewhat comical appearance, scandicimexes were graceful and deliberate climbers, and many exhibited territorial behaviors over particularly nutrient-rich climbing zones.
Scandicimexes diversified into a variety of species. Scandicimex recurvipoda was a generalist climber found across multiple forest types on central Sorlona, and was among most basal of the scandicimexis species of the Cimexian. It fed by pressing its lips to the base of dendriradix nodules, where nutrient-rich fluids seeped through the tissue. Its limbs were strong but slow-moving, favoring stability over speed. Recurvipoda was often found in pairs, showing rudimentary partner fidelity, with virifers showing submission to their matrifer partners by 'kissing' them and regurgitating extra food, similar to the behavior of bird mothers feeding their young.
Scandicimex nodifera was a species of scandicimexis that was smaller and more delicate than its cousins. Nodifera specialized in feeding on soft terraspore nodules that clustered along younger dendriradix offshoots. It used its front limbs to peel back thin membranes while feeding.
Scandicimex lingulatus was a species of scandicimexis which possessed the longest lips of the clade during the Cimexian, shaped almost like a spatula and capable of reaching into narrow radial grooves along the dendriradix’s surface. Due to its ability to extract more nutrients than most arboreal scuttlebugs, it became incredibly successful by the close of the Cimexian Epoch, and was ubiquitous throughout Eslona's dendriradix forests.
Captocimexis (Grabbing Bugs) was a a predatory offshoot of the scuttlebug lineage that emerged as terrestrial ecosystems on Atmos grew increasingly complex. They were ovivorous ambush predators and opportunistic carrion feeders, forming one of the earliest true predatory clades on land.
All captocimexes shared a fundamental body plan: a dark, low-slung form with rows of long, bristle-covered limbs for creeping over moist ground, and two major frontal appendage sets. The lower set was the graspers, which were elongated, sensitive limbs ending in multiple opposable digits or clawed pads. These were their primary tools for seizing prey, probing burrows, and manipulating delicate food like soft eggs. Above them sat a hardened, chitinized pair of pincer-mandibles, which evolved from ancestral locomotor limbs but now function as crude jaws, digging tools, or weapons.
Most species of captocimexes relied on stealth and subtle movement. They tended to operate under shadowy overhangs or along decomposing fungal matter, where egg caches were common and rotting bodies were periodically found. They stalked slowly, sometimes remaining motionless for long periods before lunging at vulnerable clusters hidden in root crevices or under fallen sporecaps. Their black or dark mottled bodies aided in camouflage, while some exhibited faint colorful spotting to confuse or attract larval prey in dim environments. While most species were exclusively ovivorous, some are scavengers, carrion feeders, and even predators, hunting scuttlebug juvenilafers. One species, Captocimexis brachychela, native to the southern tundras of Eslona, specialized in feeding on long-dead carrion. Its grasping limbs were short and stocky, built less for snatching and more for pulling apart desiccated remains. Unlike most of captocimexes, it had a partial tolerance for microbial toxins and could feed from extremely rotten sources. A specialized gut membrane allowed it to isolate digestible tissue from dangerous and indigestible meat, regurgitating what it could not digest.
One lineage of predatory scuttlebugs descended from the captocimexes, Surricaptis (Snatching Graspers), or "Snatchbugs," was a highly specialized ambush hunter that relied on lightning-fast reflexes and precision strikes to subdue its prey. The snatchbugs' agility, comparatively large size, and hunting techniques made them perhaps the most formidable predators of the late Cimexian undergrowth.
Snatchbugs were defined by their raptorial forelimbs: long, folding arms tipped with long fingers, capable of snapping shut with sudden force. These appendages were held folded against the body when at rest, giving them a compact, stalker-like profile. At the slightest motion from nearby prey, typically juvenilafer scuttlebugs, egg clusters, or small browsers, the arms lashed outward in a rapid grab, seizing and pulling the victim toward the snatchbug's mandibles.
Above the forelimbs, snatchbugs retained the hardened pincer-like mandibles of their captocimex ancestors, now used to tear apart struggling prey. Like many captocimexes, these mandibles developed long, sharp, chitinous protrusions, which functioned as aids in masticating their food. Their heads were wedge-shaped and highly mobile, with large eyes positioned on either side to provide a wide field of vision. In some species, these eyes evolved reflective layers that improved night vision, aiding in nocturnal hunting.
Unlike their stealthier ancestors, many snatchbugs were also bold and territorial. Some species performed threat displays, raising and spreading their forelimbs to appear larger when confronted by competitors or would-be predators.
Sermocimexis (Pinching Bugs), or "Shore Pincher," was a vibrant, tropics-dwelling offshoot of the scuttlebugs, adapted for life along the sun-drenched shores and humid lowland forests of Sorlona. Shore pinchers adapted oversized, claw-like forelimbs, powerful tools used for feeding, defense, and elaborate social signaling. Though unrelated to Earth’s crabs, their flattened, armored bodies, wide stance, and expressive pincers filled a similar ecological role across Atmos’s humid coastal zones and warm forested margins.
Unlike their stealthier cousins, such as the snatchbugs, shore pinchers were bold and conspicuous. Their bodies were often bright and reflective, flashing purples, blues, and reds under the intense tropical light. These colors served multiple purposes: they warned off predators, communicated dominance or mating readiness, and helped individuals recognize others of their species.
Shore pinchers were opportunistic omnivores. They lived lives quite similar to that of the ancestral scuttlebugs, foraging along beaches and within dense terraspore thickets, feeding on decaying biomass, fruiting terramats, and slow-moving prey. Their pinching limbs were strong enough to split open armored spores or pry apart soft-bodied shelled organisms that inhabit tidal crevices. While solitary individuals were common, some species were semi-social, forming loose foraging groups or sheltering together in caves, burrows, or drifting dendriradix hollows. They relied heavily on gestural displays. A lifted pincer might signal aggression, submission, or an invitation to mate, depending on posture and color shift.
Loricatucimexis (Armored Bugs) was a clade of heavily armored, burrow-dwelling scuttlebugs that emerged during the late Cimexian Epoch. Diverging early from a basal scuttlebug lineage, loricatucimexes adopted a strategy of protection and endurance. Their most defining feature was their thick, mineralized exoskeleton, an amplification of the ancestral spinal shell inherited from their pleruplod ancestors, and the semi-rigid exoskeleton derived from their scuttlebug parents. This shell, sculpted into interlocking plates and ridged carapaces, acted as a near-impervious defense against predators, environmental stressors, and other emerging threats.
Unlike the agile captocimexes or the light-footed scandicimexes, loricatucimexes were slow-moving, deliberate creatures that rarely left the safety of their shaded tunnels. Many species dug shallow burrows beneath layers of dendriradix leaf litter, terraspore sporefall, or decaying terraspore mats. Their stout, flattened legs ended in broad claws adapted for scraping through loose soil and decaying matter, allowing them to build networks of protective nests. Their enormous forward-facing eyes dominated their heads, offering excellent low-light sensitivity, a necessary adaptation for creatures that spent most of their lives in twilight underbrush or dim burrows.
Despite their slowness, loricatucimexes were well-equipped to survive in hostile environments. Their tough armor made them difficult prey for anything but the most determined or specialized predators, and protected them in their burrows against abrasion and tunnel collapse. Their diet varied by species, many were detritivores or root-grazers, consuming decaying organic matter, radiculat roots, and soft terraspore filaments.
Like the spinal shells of many of their pleruplod ancestors, their exoskeletons were often adapted for camouflage. A highland loricatucimex from northern Weslona, loricatus bombus, was mottled gray-blue, blending seamlessly with the terramats and stony terrain. It prefered to dwell beneath mats of stragulumuscs and among mossy rock crags. Unlike many of its kin, it did not burrow extensively. Instead, it lied motionless in depressions near radiculat stems, watching for passing detritus or exposed roots. Loricatus granulum was a miniature loricatucimex native to the coastal cliffs of southern Eslona. Barely larger than a seed, this species evolved armor that mimiced the coloration and texture of surrounding gravel and terraspore spore aggregates. It crept slowly through exposed pebbly terrain, surviving long periods of drought by sealing its carapace tight and entering a dormant state.
Platisentiris (Broad Feelers) was a lineage of simplified scuttlebugs descended from the sensory-focused sentirecimexes. Commonly known as "Nibbins" for their nub-like feet, these scuttlebugs were tiny and unassuming, like dust motes across the dendriradix forest floor. Nibbins were among the smallest and most ubiquitous terrestrial 'animals' on Atmos during the Cimexian Epoch. Rarely exceeding a centimeter in length, these tiny, hard-shelled creatures were slow-moving foragers that played a critical role in breaking down organic matter across the dendriradix forest floors and terrasporal beds across Sorlona, Weslona, and Eslona.
The group was characterized by their broad, flattened antennae, evolved from the thin, long sensory appendage of their sentirecimex ancestors. These widened antennae grew paddle-like and semi-rigid, sweeping gently through their environment to detect chemical cues, heat gradients, and minute vibrations. They were used not only for sensing but also for lightly brushing the ground in search of decaying spores, soft terraspore tissue, or scattered cyanophyte debris.
Unlike their more specialized predecessors, platisentirs had simplified forelimbs used exclusively for foraging. They reproduced quickly, lay dozens of tiny eggs at a time (hundreds for some species), and reached maturity in just a few days to weeks. Nibbins were a major food source for carnivorous scuttlebugs, though some species evolved mild chemical defenses or bitter-tasting outer tissue as a deterrent.
Despite their tiny bodies, nibbins were stunningly diverse. Their exoskeletal shells often displayed bright, reflective hues of fiery oranges, metallic blues, and spotted purples, the result of sexual selection and predator deterrence. Some species, like Platisentiris maculata, lived in dry fungal underbrush and flashed their speckled shells as a warning to would-be predators. Others, such as Platisentiris lurida, were nearly translucent and inhabited shaded sporebeds, feeding on terraspore threads and decaying matter. A few nibbins were arboreal, clinging to the undersides of dendriradix leaves, while others burrowed shallowly into moist soils and root clusters. Platisentiris obscura gathered in dense clusters, where their vivid exoskeletal patterns blended together so completely that distinguishing individual nubbins became nearly impossible. Platisensiris elegans exhibited a bright pattern on its back, a near-perfect mimicry of the species of dendriradix catchfronds they lived among, feeding constantly on the dendriradix's reproductive organ.
Nibbins were Atmos’s tiniest, most ubiquitous land fauna. These bulbous micro-scuttlebugs carved out an astonishing array of ecological roles in nearly every terrestrial biome. Their name reflects not just their size, but also their behavior, constantly nibbling at organic material, spores, decaying matter, or microscopic flora. Some even fed on the exudates of larger scuttlebugs, living as quiet commensals in the underbrush.
Like vorms in the seas, nibbins would be ubiquitous throughout most terrestrial environments. Look closely anywhere there is life in the Cimexian Epoch and you will find nibbins, skittering between terramat threads, burrowed amongst radiculat roots, tucked beneath terraspore spore-sacs, riding windblown debris from coast to coast.
While terramats, terraspores, and scuttlebugs flourished across the continents, the oceans of Atmos remained vibrant, dynamic realms in their own right. Even as life carved out new forms and niches on land, the seas bloomed with their own evolutionary experiments. Though some lineages found ways to bridge the aquatic and terrestrial divide, the bulk of marine evolution carried on its own grand trajectory.
Nanovormis (Little Vorms) was among the smallest known members of the vorm lineage, rarely exceeding a few centimeters in length. These tiny swimmers filled the sunlit shallows and upper pelagic zones of Atmos’ oceans, where they gathered in swarms numbering in the tens of thousands. They moved with a sinuous, flickering motion, using rapid undulations of their slender bodies and tails to maintain tight schooling formations.
Despite their miniature size, nanovorms were structurally sophisticated. Their bodies were laced with an intricate network of fine, branching blood vessels that brought oxygen and nutrients to every extremity, allowing for high metabolic efficiency and constant movement. In some species, this vascular web was faintly visible through their skin, giving them a veined appearance under the right light conditions
Though individually insignificant in mass, their collective biomass rivaled that of many larger marine grazers. This made them a crucial keystone in the open-ocean food webs of Atmos, serving as a primary food source for a wide array of filter-feeders, fast-charging scoop predators, and even some young megafauna. Their schooling behavior, a defensive adaptation, created mesmerizing displays, ribbons and clouds of nanovorms shimmering just below the surface, turning in unison as if animated by a single mind.
Gracilovormis (Graceful Vorms) was a lineage of large-bodied marine filter-feeders that flourished during the late Cimexian Epoch. Though closely related to bulkier, slow-swimming gulpers, gracilovorms were notably more agile. They swam with a partial anguilliform motion, their elongated bodies, tapered and slick, draped in a soft, rubbery skin, weaving smoothly through the water, yet they retained a thick, muscular tail used for bursts of power and maneuverability in the open ocean. Some species grew as long as a shipping container and traveled in loose aggregations that followed seasonal currents. Others were solitary wanderers of the mesopelagic zones.
Dulcevormis (Sweet Vorms) was a rotund and sluggish lineage of mid-ocean grazers that drifted through the warm, nutrient-rich gyres of the Cimexian seas. They earned their name from their glossy, brown, dimpled hides, which gave them the uncanny appearance of being molded from chocolate.
Dulcevorms resembled bloated tuna in shape, with a wide, rounded belly and short fins that fluttered inefficiently as they meandered through the water. Speed was not their strength. Instead, they relied on bulk and buoyancy, drifting slowly with currents while grazing on dense fields of microbial floc and photosynthetic plankters that bloomed near the surface.
Candadrectis (Upright Candles) was an elegant, vertically-oriented swimmers descended from the earlier adrectastachids. Where their ancestors had relied on their tails for swimming and balance, the candadrectids transformed this feature into a luminous beacon.
Living in the twilight and abyssal zones of Atmos’ deeper seas, they thrived in perpetual darkness. Their long, ribbonlike tails ended in pads of specialized photocytes capable of producing strong pulses of bioluminescence. These flashes were not simple flashes of light, they carried meaning. Different rhythms, intensities, and color variations served as a visual language, allowing groups of candadrectids to remain in tight social contact even in complete blackness.
Candadrectids swam with their heads tilted downward and their tails raised vertically like glowing wicks, their graceful bodies swaying gently in the currents. Dozens to hundreds of individuals might hover together in loose, three-dimensional clusters, flickering in sync to convey alarm, signal movement, coordinate spawning, or simply maintain cohesion. Their social complexity was among the highest of any deep-sea creature. Individuals frequently exchanged short bursts of light in paired interactions, like flickering handshakes, while entire shoals could ripple with cascading waves of light when disturbed. Though not especially fast swimmers, their unity and communication allowed them to respond to threats as a group, vanishing into the depths like a dim constellation winking out.
Pulmorepaxis (Lung Raptors) was an agile, omnivorous predator that patrolled the coastal shallows of between Sorlona and Eslona. Pulmorepaxes were efficient stalkers of small-bodied pleruplods, particularly the browsing centaur forms that clustered near tidal vegetation. Opportunistic in diet, they occasionally ingested mats of cyanophytes to supplement their energy needs during leaner times.
Over the course of several million years, a lineage of their ancestors, the cheilosrepaxes, began to shadow their prey out of the water. Much as the ancient vericataurs, ancestral scuttlebugs, had followed the land-bound terraspores onto the continents, these lip raptors began to pursue centaurs onto the wet flats left behind by the retreating tide.
Where their ancestors had been limited to the margins of the sea, darting through shallows to prey on small-bodied pleruplods, pulmorepaxes pushed boldly into the intertidal zone and beyond. Over time, they became increasingly adept at traversing the slick, broken landscapes left behind by receding tides, following their favored prey, particularly centaurs, into tidal flats and muddy shoals.
The transition was gradual but relentless. Coastal pressures favored individuals with stronger front flippers and more muscular tail bases, allowing them to drag their bodies over slick rocks and through thick mats of tidal flora. Their low, wide bodies and squat posture gave them stability and traction in the intertidal zone, and eventually, in fully terrestrial bursts.
Perhaps the most critical innovation in the pulmorepaxes’ shift toward terrestrial life was the transformation of their ancestral breathing crown. In their tristag ancestors, respiration involved drawing water in through the mouth and expelling it through lateral neck pores, extracting oxygen along the way. This system was retained and elaborated in their descendants, the dumbocoronids, where the neck pores expanded into muscular, crown-like structures. These breathing crowns became dual-purpose: extracting oxygen while also expelling water forcefully to generate bursts of propulsion through the ocean.
In the pulmorepaxes, this crown structure lost its role in movement and became specialized for extracting oxygen from air. Over millions of years, it evolved into a dense, vascularized organ that ran along the back of the head and spine. Air was drawn in through the mouth and passed across folded, moist internal surfaces within the crown-lung, where oxygen was absorbed and carbon dioxide expelled. The crown acted as a passive outflow system-breathing occurred in rhythmic cycles, with air naturally flowing from the mouth, through the internal passages, and out through the crown as the animal’s body gently expanded and contracted.
This repurposed crown-lung allowed Pulmorepaxes to forage in tidepools, splash zones, and wet coastal flats for up to an hour at a time without returning to the sea. Though they remained dependent on moisture, this respiratory innovation marked a significant step in Atmos’s long evolutionary journey toward full terrestriality.
The shift toward land also required changes in posture and mobility. Pulmorepaxes developed powerful front flippers, no longer just for steering but for pulling themselves over rocky or silty terrain. Their tails, once mainly used for aquatic propulsion, thickened at the base and developed rudimentary flexor muscles, helping to brace and pivot their movements as they hauled themselves along the shore. Though slow and cumbersome on land, they were patient and deliberate predators, using their lips to scoop up pleruplods and coastal scuttlebugs.
Over millions of years, the pulmorepaxes' descendants would further refine their ability to move and breathe on land, shedding aquatic dependency almost entirely. These terrestrial descendants, known as the Uncopeds, would become the second major lineage of Atmosian fauna to colonize the surface world after the scuttlebugs.
Unlike their moisture-bound ancestors, the uncopeds would develop powerful limb structures, enhanced terrestrial lung-crowns, and behavioral adaptations that allowed them to roam far from the coast. Their emergence marked the beginning of a new chapter in Atmos’s biospheric transformation. The arrival of the uncopeds on land would signal the end of the Cimexian Epoch and the beginning of the Uncocene Epoch, a period defined by the rise of Atmos's first megafauna.