HOLDERNESS AMMONITE

An unusual Yorkshire Holderness ammonite about 5cm across found by Harry Tabiner. He’s found a few of these specimens preserved completely with calcite making them hard to prepare. It’s possibly Kosmoceras, a middle Jurassic ammonite.

The Geology of Yorkshire in northern England shows a very close relationship between the major topographical areas and the geological period in which their rocks were formed. The rocks of the Pennine chain of hills in the west are of Carboniferous origin whilst those of the central vale are Permo-Triassic.

The North York Moors in the north-east of the county are Jurassic in age while the Yorkshire Wolds to the southeast are Cretaceous chalk uplands. The plain of Holderness and the Humberhead levels both owe their present form to the Quaternary ice ages. The strata become gradually younger from west to east. Much of Yorkshire presents heavily glaciated scenery as few places escaped the direct or indirect impact of the great ice sheets as they first advanced and then retreated during the last ice age. This beauty is in the collection of the deeply awesome Harry Tabiner.

CORAL: CLIMATE CHANGE INDICATORS

A lovely specimen of fossilized coral. Corals are marine invertebrates within the class Anthozoa of the phylum Cnidaria. They typically live in compact colonies of many identical individual polyps.

Annual growth bands in some corals, such as the deep-sea bamboo coral, Isididae, may be among the first signs of the effects of ocean acidification on marine life. The growth rings allow geologists to construct year-by-year chronologies, a form of incremental dating, which underlies high-resolution records of past climatic and environmental changes using geochemical techniques.

Certain species form communities called microatolls, which are colonies whose top is dead and mostly above the waterline, but whose perimeter is mostly submerged and alive. The average tide level limits their height. By analyzing the various growth morphologies, microatolls offer a low-resolution record of sea-level change. Fossilized microatolls can also be dated using Radiocarbon dating. Such methods can help to reconstruct Holocene sea levels.

Increasing sea temperatures in tropical regions, ~1 degree C, over the last century have caused major coral bleaching, death, and collapsing of coral populations since although they are able to adapt and acclimate. It is uncertain if this evolutionary process will happen quickly enough to prevent a major reduction of their numbers.

Though coral has large sexually-reproducing populations, their evolution can be slowed by abundant asexual reproduction. Gene flow is variable among coral species. According to the biogeography of coral species gene flow cannot be counted on as a dependable source of adaptation as they are very stationary organisms. Also, coral longevity might factor into their adaptivity.

However, adaptation to climate change has been demonstrated in many cases. These are usually due to a shift in coral and zooxanthellae genotypes. These shifts in allele frequency have progressed toward more tolerant types of zooxanthellae. Scientists found that a certain scleractinian zooxanthella is becoming more common where sea temperature is high. Symbionts able to tolerate warmer water seem to photosynthesize more slowly, implying an evolutionary trade-off.

In the Gulf of Mexico, where sea temperatures are rising, cold-sensitive staghorn and elkhorn coral have shifted in location. Not only have the symbionts and specific species been shown to shift, but there seems to be a certain growth rate favorable to selection. Slower-growing but more heat-tolerant corals have become more common. The changes in temperature and acclimation are complex. Some reefs in current shadows represent a refugium location that will help them adjust to the disparity in the environment even if eventually the temperatures may rise more quickly there than in other locations. This separation of populations by climatic barriers causes a realized niche to shrink greatly in comparison to the old fundamental niche.

CORAL COLONIES

Coral colony and Soldier Fish, Great Barrier Reef, Australia

Corals are marine invertebrates within the class Anthozoa of the phylum Cnidaria. They typically live in compact colonies of many identical individual polyps.

Corals are important reef builders that inhabit tropical oceans and secrete calcium carbonate to form a hard skeleton.

A coral "group" is a colony of a myriad of genetically identical polyps. Each polyp is a sac-like animal typically only a few millimetres in diameter and a few centimetres in length. A set of tentacles surround a central mouth opening. Each polyp excretes an exoskeleton near the base. Over many generations, the colony thus creates a skeleton characteristic of the species which can measure up to several meters in size. Individual colonies grow by asexual reproduction of polyps. Corals also breed sexually by spawning: polyps of the same species release gametes simultaneously overnight, often around a full moon. Fertilized eggs form planulae, a mobile early form of the coral polyp which when mature settles to form a new colony.

Although some corals are able to catch plankton and small fish using stinging cells on their tentacles, most corals obtain the majority of their energy and nutrients from photosynthetic unicellular dinoflagellates of the genus Symbiodinium that live within their tissues. These are commonly known as zooxanthellae and gives the coral colour. Such corals require sunlight and grow in clear, shallow water, typically at depths less than 60 metres (200 ft). Corals are major contributors to the physical structure of the coral reefs that develop in tropical and subtropical waters, such as the Great Barrier Reef off the coast of Australia. These corals are increasingly at risk of bleaching events where polyps expel the zooxanthellae in response to stress such as high water temperature or toxins.

Other corals do not rely on zooxanthellae and can live globally in much deeper water, such as the cold-water genus Lophelia which can survive as deep as 3,300 metres (10,800 ft). Some have been found as far north as the Darwin Mounds, northwest of Cape Wrath, Scotland, and others off the coast of Washington State and the Aleutian Islands.

TUZOIA OF THE BALANG FORMATION

A large extinct bivalved arthropod, Tuzoia sinesis (Pan, 1957) from Cambrian deposits of the Balang Formation. The Balang outcrops in beautiful Paiwu, northwestern Hunan Province in southern China. The site is intermediate in age between the Lower Cambrian Chengjiang fauna of Yunnan and the Lower to Middle Cambrian, Kaili Lagerstätten of Guizhou in southwestern China.

This specimen was collected in October 2019. It is one of many new and exciting arthropods to come from the site. Balang has a low diversity of trilobites and many soft-bodied fossils similar in preservation to Canada's Burgess Shale.

Some of the most interesting finds include the first discovery of anomalocaridid appendages (Appendage-F-type) from China along with the early arthropod Leanchoiliids with his atypical frontal appendages (and questionable phylogenetic placement) and the soft-shelled trilobite-like arthropod, Naraoiidae.

Jianheaspis jiaobangensis, is a newly described trilobite also from the Lower Cambrian Balang Formation of Guizhou Province, China. While the site is not as well-studied as the Chengjiang and Kaili Lagerstätten, it looks very promising. The exceptionally well-preserved fauna includes algae, sponges, chancelloriids, cnidarians, worms, molluscs, brachiopods, trilobites and a few non-mineralized arthropods. It is an exciting time for Cambrian paleontology. The Balang provides an intriguing new window into our ancient seas and the profound diversification of life that flourished there.