Beauty itself is often not enough to prompt invertebrate research, either through the researchers themselves or the ones founding their research. This seems to be the case with today’s fellow, an absolutely beautiful but completely unstudied bryozoan, Disporella violacea, which I decided to call the Hawaiian purple bryozoan.
This is an encrusting species of bryozoan, meaning it grows firmly attached to the substrate, which can be rocks or the surface of other species with a hard skeleton, such as mollusks, especially bivalvians. It is colonial, of course, which is the rule for bryozoans, and the individual zooids are often organized circularly. The whole colony has a beautiful purple or blue tinge and appears as a flat, often irregular, purple spot with many lighter circular marks formed by the circularly-organized zooids.
Disporella violacea around Oahu, Hawaii. Photo by Craig Fujii.*
I have found a single source stating that the Hawaiian purple bryozoan is found across the Indo-Pacific, but I was only able to find photographs of colonies growing in coral reefs around Oahu in Hawaii.
What can we say about its ecology? Well, nothing. I could not find a single paper dealing with this species. We have no idea how it interacts with other species, how it reproduces, nothing! It belongs to the order Cyclostomatida, often called the cyclostomes (not to mistake for the Cyclostomata, which includes lampreys and hagfish). Cyclostome bryozoans seem to be poor competitors for space in coral reefs, being often displaced by other sessile animals such as sponge, ascidians and other bryozoans, such as the cheilostome bryozoans.
And this is what we have for today. A beautiful organism whose life history is completely unknown.
Insects and their six-legged relatives are predominantly land and freshwater species, with very few living in the sea. One of these few species is the springtail Anurida maritima, known as the seashore springtail because this is exactly where it is found.
The preferred habitat of the seashore springtail are rocky or muddy shores with crevices where they can hide when the tide gets high. They are found especially in the Atlantic coast of Europe and North America, but can reach the southern portions of South America and Africa as well.
Several seashore springtails in England. Photo by Calum McLennan.*
During the low tide, they walk around the shore looking for food, which consists mostly of dead animals, especially gastropods. The seashore springtail is, in fact, considered a very important scavenger where it occurs. About one hour before the tide gets high or when the sky darkens because rain is coming, they run toward the crevices that they inhabit and where they build their nests. Since their behavior is governed by the tide and not the day, they have a circatidal rhythm that lasts about 12.4 hours, which helps adjust it as the tide slightly changes from one day to the next as the moon moves around the earth.
Seashore springtails gathering inside the exoskeleton of a dead crab. Photo by Mary Johnson.*
They prefer places that get protected from the water current, especially where there are roots or other vegetative structures that increase protection and surface. Hundreds of springtails can get together in a single nest and get surrounded by a large air bubble when the seawater fills the space. And there they wait until the tide gets low again. They also use those nests to molt and lay their eggs, thousands of them, forming a sort of collective nest.
During winter, they all die and let only their eggs behind. In spring the eggs hatch and the shore gets full of them again, all eager to explore and eat as many dead snails as possible.
Joosse, E. N. (1966). Some observations on the biology of Anurida maritima (Guérin),(Collembola). Zeitschrift für Morphologie und ökologie der Tiere, 57(3), 320-328. https://doi.org/10.1007/BF00407599
King, P., Pugh, P. J. A., Fordy, M. R., Love, N., & Wheeler, S. A. (1990). A comparison of some environmental adaptations of the littoral collembolans Anuridella marina (Willem) and Anurida maritima (Guérin). Journal of Natural History, 24(3), 673-688. https://doi.org/10.1080/00222939000770461
It’s been 84 years since the last time we had a free-living protist as a fellow here. Today’s fellow is a freshwater shape-shifter known as Clathrulina elegans. It obviously lacks a common name, so I decided to call it the elegant clathrulina.
Adult elegant clathrulinas live inside a round organic capsule measuring about 50 µm in diameter. The cell does not occupy the whole capsule, but can move freely inside it. The surface of the capsule has several oval or polygonal openings measuring about 6 µm in diameter. The cell extends very thin pseudopods (filopods) through every opening of the capsule and uses them to capture food, usally smaller protists. These pseudopods arise from cone-like projections at the surface of the cell. Up to three pseudopods can come out of the same projection, but all three pass through different openings of the capsule. Two pseudopods never share the same opening. The capsule has a long stalk, about 150 to 200 µm in length, which attaches the organism to the substrate.
Under favorable conditions, the cells grow inside the capsule and their nucleus suffers mitosis without the whole cell dividing. If the conditions suddenly become unfavorable, the cell divides into several cells and they turn into cysts, which remain inert inside the capsule until the conditions become favorable again.
If the ideal conditions persist, the multinucleated cell eventually divides into several daughter cells. All but one of them leave the capsule and turn into either an amoeboid shape or a biflagellate shape. These amoeboid and biflagellate stages move around until they find a suitable substrate to settle, where they transform again into an adult form. This transformation is complex and starts by a complete change in shape of the cell, which becomes kind of like a sphere, and one large pseudopod is formed to become the stalk. After the stalk is formed, the cytoplasm inside the stalk retracts, letting it hollow, and several vacuoles are formed below the cell membrane, forcing the cell to be separated into an outer part that will develop into the capsule and an inner part that will remain as the cell proper.
The elegant clathrulina can be found in freshwater environments in many parts of the world. However, as it is common among unicellular organism, this may actually be a complex of several species. As usual, there are no studies to clarify the true diversity of this and many other protists.
Bardele, C. F. (1972). Cell cycle, morphogenesis, and ultrastructure in the pseudoheliozoan Clathrulina elegans. Zeitschrift für Zellforschung und Mikroskopische Anatomie, 130(2), 219-242. https://doi.org/10.1007/BF00306959
Foulke, S. G. (1884). Some phenomena in the life-history of Clathrulina elegans. Proceedings of the Academy of Natural Sciences of Philadelphia, 17-19. https://www.jstor.org/stable/4060940
We learned last week about the giant African snail and how it spread around the world, harming several ecosystems. By the beginning of the 1980s, the giant African snail was a pest on the island of Guam, but suddenly its numbers started to drop and the cause was the accidental introduction of another species on the island, the New Guinea flatworm, Platydemus manokwari.
New Guinea Flatworm in Indonesia. Foto by Franz Anthony.*
Discovered in the forests around the city of Manokwari in New Guinea, more precisely in the province of West Papua, Indonesia, the New Guinea flatworm were at first just another land planarian like many others found around Australasia and the Indo-Malaya ecozones. Measuring about 60 mm in length, 7 mm in width and only 2 mm in thickness, the New Guinea flatworm has a dark-brown, almost black dorsum with a fine yellow median line, while the ventral side has a beige color. Belonging to the tribe Rhynchodemini of land planarians, it has only two eyes near the anterior end and they are considerably large compared to the eyes of land planarians of other tribes and subfamilies and even have a simple lens over their pigment cup, meaning it probably sees better than most planarians.
Anterior end of the New Guinea flatworm. The right eye is visible as a black dot. Credits to Justine et al. (2014).**
As all, or most, land planarians, the New Guinea flatworm is a predator and its favorite prey seems to be snails, which made it become a successful control method against the giant African snail in Guam. Due to this success, the New Guinea flatworm was deliberately introduced in Bugsuk, a small island of the Philippines. About 20 months after its introduction, its population had grown significantly and the population of the giant African snail had sharply decreased.
During the following years, the interested in the New Guinea flatworms as biological control increased and the species was introduced either deliberately or accidentally in many Pacific islands. However, around the 1990s, the situation has already turned into a nightmare. One of the most severely affected areas were the Ogasawara Islands in Japan. These islands used to have a very rich snail fauna but 10 years after the introduction of the New Guinea flatworm, most species were extinct. However, despite removing most snails from the islands, the population of the New Guinea flatworm continued to be large and soon it was discovered that it could also feed on earthworms, nemerteans, woodlice and even other land planarians. Its threat, therefore, goes way beyond the snails.
Although widespread across many Pacific islands, the New Guinea flatworm remained restricted to this area of the world for some time, but things changed in 2014 when it was reported in France. Only one year later, in 2015, it was found in the southern United States and the Caribbean. By 2018 it was recorded in Thailand and, to turn things worse, it revealed to be another host of the parasitic nematode Angiostrongylus cantonensis, just like the giant African snail.
It should come as no surprise that the New Guinea flatworm is also considered one of the top 100 invasive species. Its recent spread across Europe and the Americas means that a new wave of extinctions caused by our recklessness it about to begin.
Chaisiri, K., Dusitsittipon, S., Panitvong, N., Ketboonlue, T., Nuamtanong, S., Thaenkham, U., Morand, S., & Dekumyoy, P. (2018). Distribution of the newly invasive New Guinea flatworm Platydemus manokwari (Platyhelminthes: Geoplanidae) in Thailand and its potential role as a paratenic host carrying Angiostrongylus malaysiensis larvae. Journal of Helminthology, 1–9. https://doi.org/10.1017/S0022149X18000834
Justine, J.-L., Winsor, L., Gey, D., Gros, P., & Thévenot, J. (2014). The invasive New Guinea flatworm Platydemus manokwari in France, the first record for Europe: Time for action is now. PeerJ, 2, e297. https://doi.org/10.7717/peerj.297
Justine, J.-L., Winsor, L., Barrière, P., Fanai, C., Gey, D., Han, A. W. K., La Quay-Velázquez, G., Lee, B. P. Y.-H., Lefevre, J.-M., Meyer, J.-Y., Philippart, D., Robinson, D. G., Thévenot, J., & Tsatsia, F. (2015). The invasive land planarian Platydemus manokwari (Platyhelminthes, Geoplanidae): Records from six new localities, including the first in the USA. PeerJ, 3, e1037. https://doi.org/10.7717/peerj.1037
Kawakatsu, M., Oki, I., Tamura, S., Itô, H., Nagai, Y., Ogura, K., Shimabukuro, S., Ichinohe, F., Katsumata, H., & Kaneda, M. (1993). An extensive occurrence of a land planarian, Platydemus manokwari de Beauchamp, 1962, in the Ryûkyû Islands, Japan (Turbellaria, Tricladida, Terricola). 陸水生物学報 (Biology of Inland Waters), 8, 5–14.
Muniappan, R., Duhamel, G., Santiago, R. M., & Acay, D. R. (1986). Giant African snail control in Bugsuk island, Philippines, by Platydemus manokwari. Oléagineux, 41(4), 183–186.
Ohbayashi, T., Okochi, I., Sato, H., & Ono, T. (2005). Food habit of Platydemus manokwari De Beauchamp, 1962 (Tricladida: Terrricola: Rhynchodemidae), known as a predatory flatworm of land snails in the Ogasawara (Bonin) Islands, Japan. Applied Entomology and Zoology, 40(4), 609–614. https://doi.org/10.1303/aez.2005.609
Sugiura, S. (2010). Prey preference and gregarious attacks by the invasive flatworm Platydemus manokwari. Biological Invasions, 12(6), 1499–1507. https://doi.org/10.1007/s10530-009-9562-9
A few days ago I saw a photo of some giant African snails and though “that’s an interesting species to feature as a Friday Fellow”, and to my surprise a gastropod was scheduled to be presented today, so voilà, let’s talk about Lissachatina fulica, the Giant African Snail.
As the popular name implies, this land snail is native from Africa, more precisely East Africa, around Kenya and Tanzania, and it is quite large, with adults measuring 20 cm or more in length and about 7 cm in height. The shell is conical and very hard and has a marmorated brown and white color and a sharp border around its opening.
The Giant African Snail is able to feed on a huge variety of plants and can sometimes even consume dead animals, paper and even stones. As a result, it is very adaptable to new areas and has become invasive in many regions of the world, especially tropical areas in Asia, South America and the Pacific.
These snails are hermaphrodites but when mating they can act only as male, only as female or as both and this is usually related to the size of both snails. If they are similar in size, they transfer sperm to each other. If they have different sizes, the smaller snail act as a male and the larger one as a female. A “female-acting” snail can store sperm up to two years to fertilize eggs as they are produced. Thus, a single mated “female” can create an entire population if transported to a new area as it can lay around 200 eggs per clutch and produce about five to six clutches per year.
The Giant African Snail is edible and used as a food source by some African peoples. A similar species, Archachatina marginata, native from Nigeria, is offered to West African deities which in Brazil led to the development of Candomblé. However, as this species is not found in Brazil, it is replaced by Lissachatina fulica, which has been introduced in this country. Recently it has become considerably popular as a pet as well. This species has also been studied for medical use and an antimicrobial compound has been isolated from its mucus.
Especially due to its use as a food source, but also accidentally, the Giant African Snail has ben introduced in many places around the world and has become a threat to tropical ecosystems because of its voracious behavior, where it competes with native snails for food resources. Due to the need to feed on calcium to build their shell, these snails can also end up eating calcium-rich material in buildings and cause severe damage to the structures.
A specimen in Salvador, Brazil. Photo by Clara Matos.**
More than that, the Giant African Snail can harbor a parasitic nematode, Angiostrongylus cantonensis, which causes a very serious meningitis in humans. Most cases of humans being infected by this nematode is the result of eating the snails raw, but there is a small chance of getting infected even by only manipulating the snails.
Due to so many damaging outcomes from the introduction of this species around the planet, it is considered one of the top 100 invasive species of the world. Some attempts to control invasive populations using biological agents have failed miserably and only worsened the whole scenario. Next week I will present one of those failures.
Graeff-Teixeira, C. (2007). Expansion of Achatina fulica in Brazil and potential increased risk for angiostrongyliasis. Transactions of the Royal Society of Tropical Medicine and Hygiene, 101(8), 743-744. https://doi.org/10.1016/j.trstmh.2007.03.012
Thiengo, S. C., Faraco, F. A., Salgado, N. C., Cowie, R. H., & Fernandez, M. A. (2007). Rapid spread of an invasive snail in South America: the giant African snail, Achatina fulica, in Brasil. Biological Invasions, 9(6), 693-702.
Zhong, J., Wang, W., Yang, X., Yan, X., & Liu, R. (2013). A novel cysteine-rich antimicrobial peptide from the mucus of the snail of Achatina fulica. Peptides, 39, 1-5. https://doi.org/10.1016/j.peptides.2012.09.001
We see grasses all the time around us but we barely pay attention to them, even though they form one of the most diverse plant families in the world. Today I’m presenting one of them, one that actually grows all around my parents’ house making up the lawn. Its scientific name is Axonopus compressus and its common name is often Broadleaf Carpetgrass.
The typical appearance of a lawn of broadleaf carpetgrass. Notice a lot of leaves cut from mowing the lawn. Photo by Mateo Hernandez Schmidt.*
This species is native from southern USA to northern Argentina. As all, or most, grass species used as lawn, it has a creeping habit, with shoots that come out of the subterranean rhizomes spreading horizontally over the soil. It has relatively broad and soft leaves for a grass, without much hair, and often a reddish tinge on the creeping “branches”. The inflorescences form narrow spikes that occur in groups of 2 to 3, sometimes up to 5, in the single branch that comes out from the top of a stalk that can be up to 60 cm tall. Sometimes more than one inflorescence comes out of the same stalk.
Due to the fact that the broadleaf carpetgrass grows too close to the soil, it is not popular as a food source for cattle. However, it is very common as lawn, especially because it is very tolerant to both drought and floods, full sun or shadow. It can also be used for football fields, although it is not considered an ideal species for that.
A stalk with several inflorescences with 2 to 3 spikes each. Photo by Mateo Hernandez Schmidt.*
Although native to the Americas, the broadleaf carpetgrass has been introduced in Africa, Asia and Australia and became a weed of considerable importance in some places. Even though it does not grow and spread as quickly as other grasses, it often is able to survive and sometimes even outcompete other species due to its resistance to a broad range of environmental conditions.
Several studies have indicated that the broadleaf carpetgrass can be used as an efficient agent to reduce the pollution of contaminated soils and grey water. Recent studies have also focused on the genetics of this species to understand its phylogenetic relationships and the mechanisms responsible for its remarkable resistance.
Although usually an “invisible” organism that is very present around us, the broadleaf carpetgrass is very useful to humans for a variety of purposes and probably many more are still to be discovered.
Arunbabu, V., Sruthy, S., Antony, I., & Ramasamy, E. V. (2015). Sustainable greywater management with Axonopus compressus (broadleaf carpet grass) planted in sub surface flow constructed wetlands. Journal of Water Process Engineering, 7, 153-160. https://doi.org/10.1016/j.jwpe.2015.06.004
Bordoloi, S., Basumatary, B., Saikia, R., & Das, H. C. (2012). Axonopus compressus (Sw.) P. Beauv. A native grass species for phytoremediation of hydrocarbon‐contaminated soil in Assam, India. Journal of Chemical Technology & Biotechnology, 87(9), 1335-1341.
He, L., Liao, L., Wang, Z., & Wu, Y. (2020). The complete chloroplast genome of Axonopus compressus (Sw.) Beauv. and its phylogenetic position. Mitochondrial DNA Part B, 5(2), 1441-1442. https://doi.org/10.1080/23802359.2020.1735951
Ighovie, E. S., & Ikechukwu, E. E. (2014). Phytoremediation of crude oil contaminated soil with Axonopus compressus in the Niger Delta Region of Nigeria. Natural Resources, 2014. doi: 10.4236/nr.2014.52006
Hey there, Earthling! I felt like posting something special for the blog, but since we’re still a few months away from our 10th anniversary, I’ll just do it now; today I bring a special article about a special subject: Speculative Evolution. For those who are unfamiliar with what this is, it’s simply a creative movement that is equal parts art and science, and based on questions such as “how would evolution work if things happened differently?”, “how will life look like millions of years into the future?” and even “what forms will X living being produce in given parameters?”. And while such thought-experiment is done purely for the sake of entertainment, it does provide a fun way to learn and understand how evolution and its processes function and influence life, and one might even say it can allow us to predict what we might encounter in the fossil record – more on that later!
It’s a field not so dissimilar from exobiology art, of which the focus is imagining life in other planets, and which can be a bit of an anything-goes scenario given the extreme parameters that exoplanets may produce and sheer variety of such in the known cosmos, though in some cases it really depends on how willing the artist is to deviate from the Terran paradigms; in this case, however, we’re specifically talking about alternative evolution routes for Earth’s living beings, either from the past or from the present towards the future, and it’s arguably one of the most alluring movements for creative minds who can’t help but imagine a biosphere of their own design – it’s a very big part of what made the EN group become friends.
Its popularity has gradually grown in no small part due to the works of the Scottish geologist, paleontologist and prolific dinosaur book writer Dougal Dixon, with his famous trilogy of speculative evolution consisting of “After Man: A Zoology of the Future” (1981), “The New Dinosaurs: An Alternative Evolution” (1988) and “Man After Man: An Anthropology of the Future” (1990), later as well working as consulter and creature designer for the later TV series “The Future is Wild” (2002), which was responsible for the resurgence of interest in this area by bringing a relatively more up-to-date take on the subject. With the growing presence of the internet at the time, Speculative Evolution flourished to create a fandom of its own sometime around the mid-2000s.
The result of this fanatical writing made a text so long that I decided to make it into a three-parter special:
-The first part, which you’ll read in this post, will tell you about the works that first explored the theme – most in passing – and were released before After Man.
-The second part focuses solely on Dougal Dixon’s trilogy of After Man, The New Dinosaurs, and Man After Man, and marked the de facto birth of Speculative Evolution as a genre since they were the first purposely-made works on the subject available to a global-scale public.
– The third part will talk about the works that came after Dixon’s trilogy and were influenced by it, primarily The Future is Wild, as well as more recent takes on the subject, and what the future might hold for the genre.
So with all that said, let’s explore where all of this comes from, going back to the very birth of evolutionary thought:
-Darwin’s ponders on the speculative evolutions of the bear (and fish)
This may come as a surprise to some, but Charles Darwin himself, the father of modern biology and evolutionary science, and the one who proposed the concept of natural selection and the gradual change of species through time, was one of the first scientific minds to write about the core concept of speculative evolution in some shape and form.
In the first edition of his well-known book “The Origin of Species” (1859), Darwin describes the following:
“In North America the black bear was seen . . . swimming for hours with widely open mouth, thus catching, like a whale, insects in the water. Even in so extreme a case as this, if the supply of insects were constant, and if better adapted competitors did not already exist in the country, I can see no difficulty in a race of bears being rendered, by natural selection, more and more aquatic in their structure and habits, with larger and larger mouths, till a creature was produced as monstrous as a whale.”
This excerpt was removed from the second edition due to the controversial nature of the statement, as many scoffed at the idea of a bear becoming a whale (which is, of course, absurd, since they evolved from hoofed mammals); however, this suggests that Darwin thought of how evolution, as a factual process and in an out-of-the-box approach, could, if given enough time and with the proper set of circumstances, cause a modern animal to become a fictional species with an entirely new appearance and lifestyle. That in itself is the basis of speculative evolution, and as far as anyone is concerned, it may very well be the first account of such, unlike the erroneous notions of the Lamarckian theory.
Majestic.
Furthermore, Darwin also pondered on the same process applied to the development of the flying-fish into becoming a creature capable of true flight. If it sounds too familiar a description, don’t worry, we’ll look into it later on:
“Seeing that a few members of such water-breathing classes as the Crustacea and Mollusca are adapted to live on the land, and seeing that we have flying birds and mammals, flying insects of the most diversified types, and formerly had flying reptiles, it is conceivable that flying-fish, which now glide far through the air, slightly rising and turning by the aid of their fluttering fins, might have been modified into perfectly winged animals. If this had been effected, who would have ever imagined that in an early transitional state they had been inhabitants of the open ocean, and had used their incipient organs of flight exclusively, as far as we know, to escape being devoured by other fish?”
While the idea of strange and unusual creatures inhabiting the world has always been commonplace in human culture since ancient times, they always had a fantastic and magical aspect to them, often outright breaking the laws of physics and biological understanding, which is a radically different approach of imagining life from the point of view of speculative evolution, which roots its principles on factual processes to produce fanciful life forms but with a depth of truth to them.
It’s also worth noting that creationism was the prevalent model even for scientific fields in Darwin’s time: for paleontology at its infancy, the concept of a world millions of years old, if not billions, was unfathomable, and the skeletons of creatures long gone were thought to be that of “antediluvian” monsters that inhabited the planet along with humans and regular modern animals and where correlated to the biblical mythological beasts, and contributing for such idea is the fact that their bones were frequently found buried in sedimentary rocks, suggesting they were buried by such events like a worldwide flood. This vision was challenged only after Darwin’s ideas were published and science began to be more objective, separating itself from religious views in the search for evidence to understand the natural world and its history.
Prehistoric fauna as understood in 1849
Even after the notion of extinction broke free from the stigma of going against the image of an infallible creator figure, for a time science proceeded shyly to try and explain the strange creatures analyzed and the absurd picture they painted in a reasonable manner, as the fossil record of the time didn’t provide a very clear idea of what had transpired in our world in ages past. As more and more material was found and established the progression of how living things evolved and had gone extinct, science was able to produce a much more familiar timeline for the modern reader in the early 20th century and understand how certain creatures came to be – even us.
-Early speculative evolution ideas with H. G. Wells
The classic book by the British writer H. G. Wells, “The Time Machine” (1895), can be considered what sprung the entire idea of time travel, as well as life developing after the present day to the wider media – even Dixon himself cites this work as being the inspiration behind After Man.
Other than the prominent Eloi and Morlocks, both having evolved from modern day humans hundreds of thousands of years after modern times, the book also describes a few other creatures which are a bit tame by today’s standards in sci-fi settings: the world 30 million years hence is apocalyptical, covered in lichens and inhabited by giant arthropods similar in appearance to crabs, butterflies and nautiloids.
Yet, due to the narrative nature of the work, there’s not much objective approach to the life forms described: the human descendants do possess physical and behavioral differences from their ancestors, but the circumstances that brought about these changes are superficial and seemingly included as a literary device for social commentary (that is, considering the material from the prequels, which detail the exact origins of the Eloi and the Morlocks), and the creatures from the far future seem to be created rather for shock value than any objective rationalization of why and how these forms came into existence (furthermore, material removed from the original and later on added again mention some more forms, and seemingly indicate that the creatures seen in the far future are in fact the descendants of the Morlocks and Eloi).
What?!
That’s not to discredit the notion of life existing million of years into the future being established, even if it does seem much grimmer than what most would consider for a scenario that “near” into the future nowadays, being something more suitable to several hundred million years in modern speculative evolution, and regardless it is a pretty good bet that creatures of arthropod characteristics would rule the world the further one travelled towards the future.
Just, you know, they wouldn’t be evolved from humans.
“Hide your children, hide your wife, the implications are awkward no matter what”
“The Time Machine” had, of course, various film adaptations, some of which actually removed much of the speculative elements in the original or otherwise didn’t give it a lot of attention, most glaringly the Eloi being portrayed as regular people in stature and appearance as opposed to their Hobbit-esque incarnations from the books (though it’s perfectly understandable why they changed it).
– More ideas of future evolution for humans with Olaf Stapledon
While the idea of humanity evolving into new species was already introduced with “The Time Machine”, a more elaborated take on the subject, if a more fantastic one, was presented with British philosopher and sci-fi writer Olaf Stapledon’s book, “Last and First Men” (1930), which chronicles the future of humanity in the span of 2 billion years.
As you can imagine, the sci-fi aspect has a pretty heavy influence on the concept given the unreasonable amount of time covered and the future humans varying greatly in appearance – one being a gigantic brain, while another is shaped like a bat – and some very early use of the idea of genetic engineering being employed. Sadly, the species featured weren’t illustrated as frequently as the ones from H. G. Wells’ work.
You’re either all brawl or all brains, there’s no middle ground here.
And while the book was a great success upon release and has had a lasting impact in the sci-fi, its Speculative Evolution side seemingly didn’t receive much attention, with the core idea of human evolution only resurfacing in force 60 years later with “Man After Man”, and to this day it’s one of the less explored scenarios of the field, although it does come up from time to time.
It’s also a work I haven’t heard about until recently so I don’t have a lot to say about it, but it’s intriguing to think that the subject was a already a thing, and in the 30s of all things.
– The Rhinograndentia parody
A rather unusual and comical part of speculative evolution history, the snouters, or nasobames, or Rhinograndentia, were created long before the publishing of After Man, by the German zoologist Gerolf Steiner (a most irreverent figure whose actual photos are impossible to find), published as a book entitled “Bau und Leben der Rhinogradentia” (1957) or “The Snouters: Form and Life of the Rhinogrades” in its English translation. The entire concept was inspired by the 1905 poem “The Nasobame”, by German writer Christian Morgenstern, a nonsensical text which describes a creature that walks with its many noses.
The book is basically a literary mockumentary, presenting itself as the official translation of the only remaining document on the now-submerged Pacific archipelago of Hy-yi-yi and its unique fauna by the intrepid zoologist Harald Stümpke. Said archipelago vanished from the map due to an atomic bomb test, which also vanquished all the other researchers on the Rhinograndentia that were holding a meeting in one of the islands at the time of the catastrophe.
I spared you of seeing the nastier ones.
Despite the comedic nature of the work, Steiner was able to create a rather convincing plethora of life forms of all shapes and sizes to fill in the archipelago’s unusual ecosystems, applying a great deal of his academic knowledge of zoology to create a fauna that arguably isn’t any weirder than some real animals, and adding to the realism of the work is a bit of jest from Steiner’s part by showing “evidence” of the existence of the Rhinograndentia, with various models of supposedly “stuffed specimens” exhibited at the Wiesbaden Museum in Germany, no doubt confusing and amusing lots of visitors who don’t know any better.
It also helped that Steiner treated them as real, and maintained the ruse un til the end.
And you thought the book looked creepy.
Compared to other speculative evolution works, the Rhinograndentia is usually left out of the spotlight most likely due to its lighthearted humor and bizarreness, not to mention its limited release outside of Germany, and maybe because it’s less about actual future or alternative evolution and more of a “lost world” type of fiction, but I still find it worth talking about, especially given the lengths Steiner (which sadly has passed away in 2009) went to make a museum collection of said creatures.
And with that, we reached the end of Part 1! As you can see Speculative Evolution had existed for longer than one would imagine, albeit not identified by this name, but I hope you enjoyed reading on what preceded the works of Dougal Dixon before we tackle them on Part 2!
Today we will deal with one of the classics again. Spongia officinalis, or bath sponge, is a species that has been used by humans for millenia. Belonging to the class Demospongiae, the bath sponge is the origin of the name sponge.
The bath sponge is found in the Mediterranean from a depth of 1 to 100 meters. It grows on rocks and sand in well-oxygenated waters, forming gray-colored lumps whose shape can vary considerably. Due to its sessile habits, Linnaeus originally classified it as a plant, which can still be noticed in its name, as officinalis was a common epithet used by Linnaeus to refer to plants that were edible, medicinal or otherwise useful to humans.
A bath sponge growing near the coast of southern France. Photo by iNaturalist user lcdzie.*
As most sponges, the bath sponge feeds on floating organic particles and microorganisms, which it filters by pulling water inside its body through small pores and releasing it through larger openings, the oscula. They can reproduce either asexually by budding and fragmentation or sexually. Bath sponges can be either hermaphrodites or only have one sex, or even alternate between being male and female. Sexual reproduction occurs more often from October to November, when “male-behaving” sponges release sperm into the water, which is captured by “female-behaving” ones and transported to their eggs, where fertilization occurs. The embryo starts its development inside the mother and is eventually released to settled on the substrate and develop into a tiny version of an adult sponge.
The skeleton of the bath sponge makes it a flexible but resistant material, and dead and dried specimens have a good absorptive potential. Humans have explored these properties since ancient times, starting in Greece and later spreading through the whole Mediterranean and in modern times even to the whole world. As the common name implies, the main use of the bath sponge is in bath and other cleaning activities, just like modern synthetic sponges are used. They can also be used as an absorbent material and even as a tool for painting.
Skeleton of a dead specimen in Croatia. Photo by Vladimir Tkalčić.*
Despite being a common species in the Mediterranean, its harvesting since ancient times have severely depleted some populations and even led to local extinctions. As a result, its harvesting is forbidden or limited in some areas and interested in sponge farms have increased in recent years. The cultivation of sponges together with fish seems to be a good practice because, as sponges as filter feeders, they also help remove pollutants from water.
Have you ever used a genuine bath sponge to bathe or in other activities?
Pronzato, R., & Manconi, R. (2008). Mediterranean commercial sponges: over 5000 years of natural history and cultural heritage. Marine Ecology, 29(2), 146-166. https://doi.org/10.1111/j.1439-0485.2008.00235.x
Today’s species cause mixed feelings in humans. Named Ustilago maydis, it is known as the corn smut.
A fungus, the corn smut belong to the division Basidiomycota, the same that includes the most famous mushrooms (apart from truffles and morells, which are of the division Ascomycota). As the name of the corn smut implies, it is a species associated with corn, i.e., maize, being a parasite of this important crop.
The life of the corn smut begins in the form of sporidia, single-cell organisms that grow on the surface of corn plants by budding off daughter cells in a way that resembles the growth of a yeast. When two compatible sporidia meet on the surface of the plant, they produce conjugation tubes through which they fuse and give rise to hyphae, the multicellular stage that makes up the mycelium, i.e., the mass of filaments that form the “body” of the fungus.
Sporidia of the corn smut under the microscope. Photo by Wikimedia user Ninjatacoshell.**
The hyphae grow by penetrating the corn plant and feeding on its tissues, which causes chlorosis (insufficient chlorophyll), reduced growth and eventually the formation of tumors, which often appear on the corns.
Corn smut tumors on a ear of corn. Photo by Wikimedia user Idéalités.*
The tumors harbor the teliospores, a resting spore-stage. When the tumor is mature, it releases the teliospores, which will develop into a basidium under appropriate conditions. The basidium then originates new sporidia, which are released and restart the cycle.
Teliospores of the corn smug under the microscope. Photo by WIkimedia user Heiko4.*
The tumors caused by the corn smut are edible and, in Mexico, they are considered a delicacy and known by the name huitlacoche. The price of those tumors is much higher than that of regular corn and is used in several recipies as a filling and in soups. Huitlacoche is particularly rich in lysine, one of the essential amino acids for humans. Despite this “advantages” of the corn smut as a food source, it is still a problematic corn disease wordlwide, as it can cause losses above 30% in infected crops.
Huitlacoche at sale in Oaxaca, Mexico. Photo by N. Saum.**
The conflict between the corn smut and corn plants led to amazing evolutionary developments in both organisms. Corn plants usually respond to corn smut infections with oxidative burst, which is the production of large quantities of reactive oxygen species at the site where the fungus is trying to invade. This oxidative burst cause lots of damage to the fungus’ DNA but, as a response, the corn smut developed a rather effective recombinational DNA repair system.
Due to this strong evolutionary pressure to bypass the plant defense systems, the corn smut is becoming a new model organism to study plant-pathogen interactions. This is increased by the fact that it is a well-suited organism for genetic modification and its entire genome has already been sequenced. The study of its DNA-repair mechanisms can also lead to the development of new DNA-repairing tools and may assist in new technologies to fight against cancer.
Sometimes humans turn an original nuisance into a new oportunity to thrive because… humans. We are kind of the mammal equivalent of a cockroach afterall, aren’t we?
Brefort, T., Doehlemann, G., Mendoza-Mendoza, A., Reissmann, S., Djamei, A., & Kahmann, R. (2009). Ustilago maydis as a pathogen. Annual review of phytopathology, 47, 423-445. https://doi.org/10.1146/annurev-phyto-080508-081923
Kämper, J., Kahmann, R., Bölker, M., Ma, L. J., Brefort, T., Saville, B. J., … & Birren, B. W. (2006). Insights from the genome of the biotrophic fungal plant pathogen Ustilago maydis. Nature, 444(7115), 97-101. https://doi.org/10.1038/nature05248
Steinberg, G., & Perez-Martin, J. (2008). Ustilago maydis, a new fungal model system for cell biology. Trends in cell biology, 18(2), 61-67. https://doi.org/10.1016/j.tcb.2007.11.008
Here is a list of species described this month. It certainly does not include all described species. You can see the list of Journals used in the survey of new species here.
Caridina mayamareenae is a new freshwater shrimp from Sulawesi. Credits to Klotz et al. (2021).*Valenciolenda fadaforesta is a new cave-dwelling planthopper from Spain. Credits to Hoch et al. (2021).*
Coomaniella (Coomaniella) dentata is a new jewel bettle from China. Credits to Song (2021).*Head of a worker of Cataglyphis fritillariae, a new ant from Iran. Credits to Khalili-Moghadam et al. (2021).*
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License.
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