Friday, September 30, 2022

the month in snapshots

rocking the baby to sleep


Ainsley is damned cute


enjoying some Sunday afternoon napping with Ainsley


my three youngest beauties


the older minions


candids at the park #1


candids at the park #2


picked up a new Blackstone grill and broke it in with pork chops


Monday, September 26, 2022

Dino of the Week: Aurornis

Type Species: Aurornis xui
Classification: Dinosauria – Saurischia – Theropoda – Coelurosauria – Maniraptora – Paraves – Avialae - Anchiornithidae
Time Period: Late Jurassic (or Early Cretaceous)
Location: China
Diet: Insectivore 

The paravian Aurornis lived sometime between the Late Jurassic and Early Cretaceous. The type specimen was acquired from a fossil dealer in China and labeled as coming from the Tiaojishin Formation of the Oxfordian age of the Late Jurassic; however, those studying the fossil retroactively suggested it may have actually come from the Yixian Formation which dates back to the Early Cretaceous (Barremian and Aptian ages). Aurornis resembled Anchiornis in a number of ways (hence being in the same family group, Anchiornithidae), and some scientists believe that Aurornis is actually a variant species of Anchiornis (given that the differences between the two fall within the ‘range of variation’ expected within a single genera). Aurornis was the size of a pheasant, reaching only twenty inches in length. It had clawed wings and a long, bony tail. Its leg bones were similar to those of Archaeopteryx, but overall its anatomy was more primitive. Its primitive bone structure implies that it lacked the range of motion needed for ‘flight strokes,’ and though its whole body was covered in feathers, it lacked flight-capable feathers. Thus Aurornis may have been a ‘ground-runner’ or even lived in the trees. It may have hunted insects and worms that lived among the litter of the forest floor. 

Monday, September 19, 2022

Dino of the Week: Aorun

a pair of juvenile Aorun play together
Type Species: Aorun zhaoi
Classification: Dinosauria – Saurischia – Theropoda – Coelurosauria
Time Period: Late Jurassic
Location: China
Diet: Carnivore 

The predatory theropod Aorun is known from one specimen, and that one a juvenile that was probably around one year old (according to bone pathology). This toddler’s remains included parts of the skull, the lower jaws, a neck vertebra, a dorsal vertebra, three tail vertebrae, the left ulna and hand, the lower ends of both pubes, and both lower legs. In life it would’ve reached just over three feet long and would’ve weighed just four pounds. The length and weight of adults are unknown. Our single Aorun specimen has multiple infantile morphologies, such as enormous sclerotic rings around the eyes composed of overlapping ossicles, and teeth that either have no serrations or bear very fine serrations (such dental variability may be due to its young age). Aorun lived 160 million years ago during the Oxfordian age of the early Late Jurassic. Its remains were found in the Shishugou Formation of China, which during prehistoric times was covered by marshland and adjoined a small mountain range peppered with volcanoes. This formation has revealed that the environment was home to numerous dinosaurs, small crocodilians and amphibians, and pterosaurs. Dinosaur contemporaries of Aorun included ornithischians, sauropods, and other theropods. Aorun, at least in a juvenile state, likely hunted small lizards and mammals. 

Some scientists believe Aorun is the oldest known coelurosaur. The coelurosaurs are a subgroup of theropod dinosaurs that contains all theropods more closely related to birds than to carnosaurs (to which megalosaurs, spinosaurs, and allosaurs belong). Coelurosaurs include compsognathids, tyrannosaurs, ornithomimosaurs, and maniraptors. The maniraptors include birds, which is the only dinosaur group alive today. Because most of the feathered dinosaurs discovered so far have been coelurosaurs, some scientists – such as the preeminent Philip J. Currie – believe it probably that all coelurosaurs (such as Aorun) were feathered. 

Monday, September 12, 2022

Dino of the Week: Anchiornis

Type Species: Anchiornis huxleyi
Classification: Dinosauria – Saurischia – Theropoda – Coelurosauria – Maniraptora – Paraves – Avialae - Anchiornithidae
Time Period: Late Jurassic
Location: China
Diet: Carnivore 

The feathered paravian Anchiornis became the first Mesozoic dinosaur species for which almost its entire ‘life appearance’ could be determined, and it was an important source of information on the early evolution of birds. Anchiornis is one of many paravian theropods discovered from the Tiaojishan Formation of China. This bone-bed gives us a snapshot of the Oxfordian stage of the early Late Jurassic in southern Laurasia. Anchiornis and its ilk lived in a subtropical to temperate climate that was warm and humid. The mountainous landscape was overshadowed by brooding volcanoes that had a penchant for erupting, and the area was cut by mountain streams and deep sapphire lakes choked by dense gymnosperm forests. The jungle-like forest consisted of ginkgoes and conifers, lycopsids and horsetails, cycads and ferns. Many creatures called this place home: small feathered dinosaurs, numerous pterosaurs, salamanders and insects and arachnids. There were early mammals – including the earliest gliding mammal Volaticotherium and an aquatic protomammals Castorocauda. Interestingly, there are no ‘large’ animals present in the fossilized record of the Tiaojishan Formation.



Though we know that southern Laurasia was host to large dinosaurs – for other Chinese bone-beds have preserved sauropods, stegosaurs, early ornithopods and ceratopsians, and medium- to large-sized theropods – there are none present in this part of China (the largest creature preserved at Tiaojishan is the two-foot-long heterodontosaur Tianyulong!). Researchers have posited two main theories to explain the absence of larger organisms. The first explanation is that maybe these larger creatures simply didn’t live in this environment. Maybe the mountainous terrain was too difficult to navigate, or maybe the jungle-like forest, lush from the common nutrient-rich volcanic eruptions, was too difficult for larger animals to penetrate? These factors would be no match for smaller animals such as the panoply of paravian dinosaurs, pterosaurs, amphibians, and mammals that Tiaojishan does preserve. Another explanation is that larger dinosaurs were present in the environment, but they escaped the periodic volcanic eruptions that deposited fine dust and ash. The exquisite preservation of the Tiaojishan fossils is due to the unique volcanic sedimentary rock in which they’re preserved; this has allowed us to examine them closely and see features – such as feathers – that are usually destroyed. That these animals were entombed in volcanic ash is a given. Perhaps when the volcanoes erupted, the larger organisms – the stegosaurs and larger theropods – were able to flee whereas smaller animals were doomed, buried quickly as the ash layer built up. Marine organisms would be choked as the waterways and lakes turned to ashen mush; extreme heat and volatile air currents would damage pterosaur membranes or send them careening to the ground; and the ash would cake the feathers of the feathered paravians, weighing them down and consigning them to their deaths. In a very real way, the Tiaojishan Formation may be a series of snapshots of recurring Oxfordian apocalypses.

The handful of Anchiornis specimens preserved met their demise in volcanic ash, but their particular fossilization has given us a wealth of information about them. Anchiornis were crow-sized, four-winged, feathered paravians; they grew a little over a foot in length, weighed around half a pound, and had a wingspan of up to twenty inches. Their triangular-shaped skulls shared characteristics in common with dromaeosaurs, troodontids, and more primitive avialans. They had long, wing-bearing arms, long legs, and a long tail. Like all paravians it was covered in feathers, though it also had scales on some parts of its body. It was a carnivore, and we know this because some specimens had ‘poop pellets’ in inside their bodies when they died (making Anchiornis the earliest theropod known to have produced pellets). These pellets contained lizard bones and fish scales. 

Anchiornis’ feathers were exquisitely-preserved, so we know a lot about what it looked like. The wings, legs and tail supported long but relatively narrow vaned feathers. Two types of simpler, downy (in science-speak, plumaceous) feathers covered the rest of the body. Long, simple feathers covered almost the entire head and neck, torso, upper legs, and the first half of the tail. The rest of the tail bore contour (in science-speak, pennaceous) feathers that resembled retrices (larger feathers that most modern birds use for steering in flight; but Anchiornis, as we’ll see, likely didn’t fly). Its head bore long crown feathers that may have formed a crest. Anchiornis’ body plumage consisted of short quills with long and independent flexible barbs; these barbs stuck out from the quills at low angles on two opposing blades. This arrangement gave each feather a forked shape and resulted in Anchiornis having a softer textured and ‘shaggier’ plumage than is seen in modern birds. ‘Shaggy’ contour feathers probably served to help with thermoregulation and water repellance abilities; combining these shaggy feathers with the open-vaned wing feathers, and Anchiornis had decreased aerodynamic efficiency. 

Anchiornis’ wings were composed of eleven primary feathers and ten secondary feathers. The wing feathers had curved, symmetrical central quills; these were small and thin with rounded tips, which would’ve hindered aerodynamic abilitiy. In the paravians Microraptor and Archaeopteryx, the longest wing feathers were those nearest the wrist, making the wings appear long and pointed; Anchiornis had a different arrangement in which the longest wing feathers were those nearest the wrist, making the wing broadest in the middle and tapering near the tip for a more rounded (and less flight-adapted) profile. Anchiornis had a propatagium – a flap of skin connecting the wrist to the shoulder and rounding out the wing’s front edge – and this part of the wing was covered in covert feathers (the shorter feathers covering the bases of the longer feathers) that smoothed wing and covered the gaps between the larger primary and secondary feathers; but unlike modern birds, these feathers weren’t arranged in tracts or rows. In some Anchiornis specimens, several layers of wing feathers extend down to cover most of the wing’s surface, so that the wing is essentially composed of multiple layers of feathers. This multi-layered wing arrangement may have helped strengthen the wing. Anchiornis had three clawed fingers; the longest two fingers were bound together by the skin and other tissue forming the wing, so Anchiornis was functionally two-fingered. These bound fingers were incorporated into the post-patagium that supported the bases of the main wing feathers. Tiny, rounded scales covered the bottom of the fingers. 

Anchiornis’ legs were covered in long, vaned feathers. This has led some researchers to view Anchiornis as a four-winged theropod, much like Microraptor and Sapeornis; however, the feathers on the hind legs didn’t have the shape or arrangement suspected from flight feathers, so their role was likely display rather than aerodynamics. Anchiornis’ long legs indicate that it was a fast runner, but the extensive leg feathers would’ve prevented it from reaching any decent speeds; thus the long legs may be a vestigial feature rather than an adaptation to its environment. Anchiornis had four toes on its foot, with the third and fourth toes being the longest. The first toe – the hallux – wasn’t reversed, as we see in perching paravians. The hind-wings were shorter than those of Microraptor and were composed of twelve to thirteen feathers anchored to the lower leg and ten to eleven on the upper foot. The hind wing feathers were longest closer to the body while the short foot feathers directed outward, almost perpendicular to the foot bones. Anchiornis’ feet were covered in feathers (except for the claws). Some specimens have preserved scales on the toes, tarsus, and even lower leg, suggesting that scales were present beneath the feathers. The underside of the toes were fleshy pads with distinct creases at the joints. These pads were covered in small, pebble-like scales. 

The ultimate question, of course – the one everyone’s asking – is, “Did Anchiornis fly?” Feathers don’t necessitate flight ability (they likely evolved for thermoregulation or display; flight was a happy byproduct in some paravian lineages). We’ve already seen that Anchiornis has several features that dampen flight ability, but can we know for sure? In 2016, scientists set out to answer whether Anchiornis could fly. They determined that juvenile specimens may have been able to use their wings to assist running up an incline (a nice advantage in the mountainous terrain of their habitat), and they may have achieved flapping flight if a very high-angle flapping wing stroke was used. This would’ve been an ungainly flight and nothing pretty to see. Adult Anchiornis lacked the ability to gain any aerodynamic benefit from their wings, for they were simply too heavy. However, by flapping the wings while running, they could have increased their running speed by twenty percent. Flapping the wings while leaping would result in a fifteen to twenty percent increase in height and distance. All this to say that while juvenile Anchiornis may have been able to enjoy something like powered flight, adult Anchiornis didn’t have this ability. Their feathered wings may have helped them make ‘leaps and bounds’ as ground-runners, but they would’ve remained terrestrial. Another factor against flight is the fact that Anchiornis seems to have lacked a breastbone; some argue that it may have been made out of cartilage rather than bone (as in some more primitive theropods), but they’re at a loss to explain why the cartilage would not be preserved whilst feathers were. 

In 2010 scientists studied the distribution of Anchiornis’ melanosomes (the pigment cells that give feathers their color). By studying the types of melanosomes Anchiornis had and comparing them with those modern birds, scientists were able to map the specific colors and patterning present on the specimen when it was alive. The scientists found that most of Anchiornis’ body feathers were gray and black; the crown feathers (on the head) were rufous (reddish-brown) with a gray base and front; the face had rufous speckles among predominantly black head feathers; the forewing and hindwing feathers were white with black tips; the shorter feathers covering the bases of the long wing feathers (in science-speak, coverts) were gray, contrasting the mainly white main wings. The larger coverts of the wing were white with gray or black tips, forming rows of darker dots along mid-wing. These took the form of dark stripes or even rows of dots on the outer wing but a more uneven array of speckles on the inner wing. The shanks of the legs were gray other than the long hindwing feathers; and the feet and toes were black. In 2015, a second specimen was studied similarly, but only gray-black type melanosomes were found. Even the crown feathers were gray-black. This difference has been explained in several ways: perhaps the melanosomes were damaged or not preserved the same way; perhaps this Anchiornis was another species than the one previously studied; or maybe this was due to gender (it could very well be that males were brightly colored to attract mates and compete with other males for the ‘blander-looking’ females). Below is a portrait of the 2010 Anchiornis, a fairly accurate representation of what it looked like “in real life.”



Monday, September 05, 2022

Dino of the Week: Ambopteryx

Type Species: Ambopteryx longibrachium
Classification: Dinosauria – Saurischia – Theropoda – Coelurosauria – Maniraptora – Paraves – Scansoriopterygidae 
Time Period: Late Jurassic
Location: China
Diet: Omnivorous? 

The non-avian theropod Ambopteryx is known from a nearly complete skeleton with preserved soft tissues. This small critter was just a foot long snout-to-tail, and it had a wing membrane preserved as a continuous brownish layer on the matrix surrounding the left hand, right forelimb, and abdomen. This thin membrane may have been reminiscent of that equipped by modern bats. Ambopteryx’s head, neck, and shoulders were coated with a dense layer of feather. Its head was short and blunt, and it had a hyper-elongated third finger. Some researchers believe that this finger was used to extract grubs from wood, but others believe it was elongated for the attachment of the patagium (wing membrane) and that, in life, their fingers were encapsulated by membranous tissue and had limited mobility. Unlike most non-avian theropods, it had a short tail that lacked a transitional point and ended in a pygostyle (a set of fused tail vertebrae to support tail feathers and musculature). The only other non-avian theropods known to have a pygostyle were a handful of oviraptosaurs and therizinosaurs. Ambopteryx’s abdominal region contained a small number of gastroliths and crushed bones, likely the remnants of its last meal. The presence of both bones and gastroliths indicate it may have been an omnivore. 

Ambopteryx belongs to the non-avian Scansoriopterygid dinosaur family. Only a few species of these scansoriopterygids are known, but these reveal that they had clear adaptations for an arboreal (tree-dwelling) lifestyle and that they likely glided from branch-to-branch, spending little time on the forest floor. These were some of the smallest dinosaurs, some no larger than a sparrow. 

Friday, September 02, 2022

Dino of the Week: Chungkingosaurus


Type Species: Chungkingosaurus jiangbeiensis
Classification: Dinosauria – Ornithischia – Thyreophora – Stegosauria – Huayangosauridae 
Time Period: Late Jurassic
Location: China
Diet: Herbivore 

The stegosaur Chungkingosaurus was discovered in the Shaximiao Formation of China. This bone-bed dates back to the Oxfordian stage of the Late Jurassic, and this stegosaur is one of three stegosaurs found in the environment (the other two are Chialingosaurus and Tuojiangosaurus; some believe Chialingosaurus and Chungkingosaurus are the same animal). Contemporaries of Chungkingosaurus included sauropods such as Mamenchisaurus and Shunosaurus, theropods such as Yangchuanosaurus and Gasosaurus, and ornithischians such as the early ornithopod Agilisaurus and a heterodontosaur holdout from the earlier Jurassic known as Tianyulong

Two Chungkingosaurus specimens have been found; both were adults, with one thirteen feet long and the other sixteen and a half feet long. This could be a matter of sexual dimorphism, though stegosaurs have traditionally been interpreted as loners (though some stegosaurs may have traveled in small family groups). Chungkingosaurus resembled in many ways its larger contemporary Tuojiangosaurus, which lived in the same environment. Subtle differences between the two include the fact that Chungkingosaurus was smaller, had a deeper snout and front lower jaws (resulting in a high, narrow skull), and non-overlapping teeth with less pronounced denticles. Chungkingosaurus’ hips and humerus are more primitive than more derived stegosaurs. The deep skull may be a relict of a primitive trait or an adaptation for supporting stronger muscles for eating tougher vegetation. This stegosaur had two rows of plates and spikes on its back; they were arranged in pairs, but the total number is unknown (though most scientists believe it had fourteen rows of plates). Its plates were thickened in the middle, as if they were modified spikes, and they resemble those of Tuojiangosaurus. The thagomizer – the tail spikes used as a defensive weapon – are known only from one specimen. Its thagomizer consisted of two pairs of obliquely vertical stout spikes. It may have had a third pair towards the front of the back two pairs that was present when the specimen was discovered but lost during the excavation. A unique feature of its thagomizer was an additional pair of spikes at the very end of the tail; these were long, thin spikes oriented horizontally, giving the full thagomizer a ‘pin-cushion’ spike array. 

where we're headed

Over the last several years, we've undergone a shift in how we operate as a family. We're coming to what we hope is a better underst...