Monthly Archives: August 2020

New Species: August 2020

by Piter Kehoma Boll

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.

Tichowtungia aerotolerans is a new bacterium of the small phylum Kiritimatiellaeota. Credits to Mu et al. (2020).*

Bacteria

Nonomuraea nitratireducens is a new actinobacterium isolated from the rhizosphere of the plant Suaeda sutralis in China. Credits to Ou et al. (2020).*
Trebonia kvetii is a new genus of actinobacteria foun in the Czech Republic. Credits to Rapoport et al. (2020).*

Archaeans

Excavates

SARs

Sonerila cardamomensis is a new melastomatacean from Cambodia. Credits to Shin et al. (2020).*

Plants

Schizanthus carlomunozii is a new solanacean from Chile. Credits to Morales-Fierro et al. (2020).*

Fungi

Scheffersomyces jinghongensis is a new yeast from rotten wood in China. Credits to Jia et al. (2020).*
Junghuhnia subcollabens is a new crust fungus from China. Credits to Du et al. (2020).*

Poriferans

Cnidarians

Flatworms

Paraba tata is a new land planarian from Brazil. Credits to Oliveira et al. (2020).*

Mollusks

Nemerteans

Annelids

Bryozoans

Kinorhynchs

Nematodes

Tardigrades

Arachnids

Crustaceans

Holocerus devriesei is a new grasshopper from Madagascar. Credits to Skejo et al. (2020).*

Hexapods

Trioza turouguei is a new jumping plant louse from Taiwan. Credits to Tung et al. (2020).*

Echinoderms

Agnathans

Actinopterygians

Pristimantis chamezensis is a new frog from Colombia. Credits to Acosta-Galvis et al. (2020).*

Amphibians

Acanthosauria liui is a new agamid lizard from China. Credits to Liu et al. (2020).*

Reptiles

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*Creative Commons License This work is licensed under a Creative Commons Attribution 4.0 International License.

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Friday Fellow: Common Pellia

by Piter Kehoma Boll

Liveworts often live in moist and shady spaces and, even if we know how to identify them as liverworts, they often look all the same. However, if we pay attention to the details, differences can often be perceived.

Pellia epiphylla, commonly known as the common pellia, is a liverwort that loves very humid places, so it often grows very close to rivers and other watercourses in North America, Europe, North Africa and some nearby areas in Asia. Its thalli are smooth and slightly fleshy, about 1 cm wide and can reach several cm in length. They like ro remain in a horizontal position, so they grow very attached to the horizontal subtrates but tend to grow away in vertical ones, acquiring a more ruffled aspect. Although usually completely green, the thalli can have a purplish or reddish tinge along the middle, especially when they grow too far from water, which can help identify this species. Otherwise it is very featureless compare to many other liverworts.

File:Pellia epiphylla7 ies.jpg
The typical aspect of the common pellia. Some thalli can be seen with a purplish tinge in the middle. Photo by Frank Vincentz.**

As with all liverworts, the thallus of the common pellia is the gametophyte, i.e., the haploid generation (with only one chromosome of each type per nucleus) and that generates the gametes. Although in many liverworts the gametophytes are either male or female, they are monoicous (i.e, hermaphrodites) in the common pelia. The male sex organs (antheridia) occur along the middle, appearing as very small light and shiny dots, while the female ones (archegonia) occur close to the tip and remain covered. Fertilization, as usually, occurs when the plant becomes wet. The antheridia absorb water to the point that they burst, releasing the sperm cells (antherozoids) that swim to the archegonia, where fertilization occurs.

Young sporophytes growing from inside the archaegonia. Photo by Hermann Schachner.

The resulting zygote gives rise to the sporophyte, a diploid generation (with two chromosomes of each type per nucleus) and it grows from inside the archegonia in the form of a very long and slender whitish stalk with a dark capsule at the tip. When the capsule is mature, it bursts and releases the spores, which will germinate and originate new gametophytes. The group of sporophytes growing from the gametophyte give the set a peculiar “hairy” aspect, which also helps recognize this species.

When the sporophytes grow, they give the family a hairy look. Photo by Roger Griffith.

Being a common species across its range, the common pellia has been studied to understand physiological and reproductive characteristics of liverworts, as well as some ecological aspects. For example, it is known that, while the gametophyte absorbs water mostly through the under surface, the antheridia absorb it from the upper surface, and the lower midrib of the plant compared to the border is essential to retain water for this. While the sporophyte of many liverworts is completely dependent on its mother, the gametophyte, to receive water, that of the common pellia is much more indepenent, absorbing most of it from the environment.

Although fairly featureless, the common pellia still has its charm.

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References:

Clee A (1939) The Morphology and Anatomy of Pellia epiphylla considered in Relation to the Mechanism of Absorption and Conduction of Water. Annals of Botany 3(1): 105–111. https://doi.org/10.1093/oxfordjournals.aob.a085045

Greenwoo HE (1911) Some Stages in the Development of Pellia epiphylla. The Bryologist 14(4): 59-70. https://doi.org/10.2307/3238074

Wikipedia. Pellia epiphylla. Available at <https://en.wikipedia.org/wiki/Pellia_epiphylla >. Access on 27 August 2020.

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Friday Fellow: Rat Acanthocephalan

by Piter Kehoma Boll

The evolution of similar traits in distantly related species is common when they have similar lifestyles, and this is particularly noticeable in some parasitic groups. Among flatworms, tapeworms have developed a complex life cycle with two hosts, larval stages and adults that live in the intestine of the definitive hosts where they absorb nutrients directly through the body surface, lacking a digestive system, and have a special structure on their head to remain attached to the host’s guts.

A very similar lifestyle and morphology evolved in a distantly related group of animals, the acanthocephalans or thorny-headed worms. For a long time, the acanthocephalans were considered a phylum of their own, Acanthocephala, but we now know that they are just a group of very specialized rotiferans, whose free-living forms are very small, so small that they are often mistaken for ciliates or other unicelular organisms.

Today’s species is an acanthocephalan that lives very close to humans, so close that they can even live inside us. Named Moniliformis moniliformis, I will call it the “rat acanthocephalan” because, well, it infects rats (and occasionally other mammals including humans).

Adults of the rat acanthocephalan are often found in the intestine of rats but other mammals can also be infected, such as dogs, cats and humans. Males reach up to 5 cm in length while females can be much longer, up to 30 cm.

Adult, probably female, specimen of the rat acanthocephalan.

The anterior end of the body has a short cylindrical proboscis covered by hooks, which the animal uses to attach to the host’s intestine. This proboscis is hollow and can be pulled back into the body. There is a septum separating the cavity of the proboscis from the cavity of the rest of the body. Like in tapeworms, the surface of acanthocephalans is covered by a syncytium, a tissue formed by cells that fused together into a single multinucleated structure. Due to the lack of a digestive system, they absorb the nutrients from the hosts intestine directly through their body surface, just like in tapeworms.

Anterior end showing the short proboscis.

After mating occurs, females release fertilized eggs into the host’s intestine and they leave the body with its feces. The eggs measure about 100 µm in length and 60 µm in width and contain the first larval stage, known as the acanthor. In the environment, the eggs are ingested by the intermediate host, usually a cockroach or sometimes a beetle, and the acanthor hatches, changing into the second-stage larva, the acanthella. After some weeks developing inside the intermediate host, the acanthella changes into the final larval stage, the cystacanth, which forms a cyst inside the intermediate host’s tissues, and there it waits.

An egg under the microscope.

For the cycle to be completed, the intermediate host needs to be eaten by the definitive host. To increase the chances of this happening, the parasite leads to behavioral changes in the intermediate hosts. Infected American cockroaches, for example, show delayed escape responses, increasing the probablity of being captured by a predator. When it happens, the cystacanths are released into the definitive host’s gut and develop into adults.

File:Moniliformis moniliformis life cycle.gif
Life cycle of the rat acanthocephalan.

Humans acting as definitive hosts is a rare occurrence since it requires the ingestion of raw infected cockroaches or beetles. Most reported cases in the literature include small children, which are prone to put everything into their mouths, and the symptoms of the infection include acute abdominal pain and, in very small children, usually less than a year old, more severe symptons such as vomiting, anorexia and diarrhea can also occur. The identification of eggs in stool samples of infected humans is difficult, though, so that the actual infection rate may be much higher than thought, especially in rural areas where insect consumption is a common practice.

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References:

Moore J (1983) Altered Behavior in Cockroaches (Periplaneta americana) Infected with an Archiacanthocephalan, Moniliformis moniliformis. Parasitology 69(6):1174–1176. https://doi.org/10.2307/3280893

Salehabadi A, Mowlavi C, Sadjjadi SM (2088) Human Infection with Moniliformis moniliformis (Bremser 1811) (Travassos 1915) in Iran: Another Case Report After Three Decades. Vector-Borne and Zoonotic Diseases 8(1):101–104. http://doi.org/10.1089/vbz.2007.0150

Wikipedia. Moniliformis moniliformis. Available at < https://en.wikipedia.org/wiki/Moniliformis_moniliformis>. Access on 20 August 2020.

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Friday Fellow: Dragon Tree

by Piter Kehoma Boll

When the seventh generation of pokémon was released, it introduced regional forms of previous pokémon, including an Alolan form of Exeggutor which was changed from the grass/psychic type of the traditional Exeggutor to a grass/dragon type. This led many people to become familiar with the genus Dracaena, a genus that is well-known among botanists and gardeners and includes many ornamental plants.

Alolan Exeggutor, a grass/dragon pokémon.

The name Dracaena comes from the greek word meaning dragoness, i.e., a female dragon and is given based on the type-species of the genus, Dracaena draco, or the dragon tree, which is today’s fellow.

Dragon tree in Tenerife, Canary Islands. Photo by Wikimedia user Losrealejos.es*

The genus Dracaena is closely related to the genus Asparagus and the dragon tree was intially named Asparagus draco by Linnaeus and later renamed Dracaena draco by himself based on a genus name created by the Italian naturalist Domenico Agostino Vandelli. This species is native from the African islands in the Atlantic (Canary Islands, Cape Verde and Madeira).

Closeup of a flower. Photo by Wikimedia user Philmarin.**

The dragon tree starts its life as a small unbranched stem like most ordinary species of Dracaena we see in gardens. Its growth is very slow and only after growing vertically for 10 to 15 years it will produce flowers for the first time. The flowers are white and lily-like and appear in a spike, later turning into reddish berries. After this first reprouctive cycle, the stem branches for the first time from a crown of terminal buds and then grows again for 10 to 15 years before branching again. Being a monocot, the dragon tree lacks growth rings but its age can be estimated by the number of branching points from the ground to the crown.

File:Starr-120403-4177-Dracaena draco-fruit and leaves-Kula-Maui (24842899630).jpg
The fruits. Photo by Forest & Kim Starr.***

The association of this plant with dragons comes from ancient times. Not only Dracaena draco, but some other species of Dracaena as well, produce a red resin that is secreted when the leaves or the trunk are cut. A similar red resin is found in many other plants, including palm trees and crotons, and they were all collectively known as “dragon’s blood” and used for several purposes, such as dye or medicine. The ancient Romans collected dragon’s blood from the Island of Socotra, where a closely-related species, Dracaena cinnabari, the dragon’s blood tree, is found.

Plucked dead leaves showing the red color of the dragon’s blood. Photo by Wikimedia user Sharktopus.*

The dragon tree is the official tree of Tenerife, where the largest and possibly oldest specimen is also found, the so-called “Drago Milenario”. This specimen is about 21 m tall but, despite its name (the thousand-year-old dragon), it is not actually that old and its age is most likely about 300 years or so.

The Drago milenario in Tenerife, the largest dragon tree in the world. Photo by Andrey Tenerife.**

Despite being a relatively popular species that is grown as an ornamental plant, the dragon tree is classified as vulnerable in the IUCN’s red list. It’s wild populations are close to extinction and one reason for this is likely because some of its original seed dispersers went extinct. Only two bird species have been recently recognized as effective dispersers. Due to the dragon’s tree relatively large fruit, most bird species do not eat the whole fruit and only bite off pieces of the pulp, so that seeds are not carried to new locations.

File:Dracaena draco 1.jpg
Ripe fruits. Photo by Wikimedia user Nadiatalent.*

The Guanches, the aboriginal people of the Canary Islands, used to worship a large dragon tree in Tenerife. Alexander von Humboldt apparently saw this tree when visiting the island and it was later destroyed by a storm that hit Tenerife in 1868. The Guanches were wiped out by the Spanish invaders and now their sacred tree is facing the same fate.

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References:

Bañares A et al. (1998) Dracaena dracoThe IUCN Red List of Threatened Species 1998: e.T30394A9535771. https://dx.doi.org/10.2305/IUCN.UK.1998.RLTS.T30394A9535771.en. Access on 13 August 2020.

González-Castro A, Pérez-Pérez D, Romero J, Nogales M (2019) Unraveling the Seed Dispersal System of an Insular “Ghost” Dragon Tree (Dracaena draco) in the Wild. Frontiers in Ecology and Evolution 7:39. https://doi.org/10.3389/fevo.2019.00039

Wikipedia. Dracaena draco. Available at < https://en.wikipedia.org/wiki/Dracaena_draco >. Access on 13 August 2020.

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**Creative Commons License This work is licensed under a Creative Commons Attribution-ShareAlike 4.0 International License.

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Friday Fellow: Lab Dung Fungus

by Piter Kehoma Boll

In my microbiology classes as an undergraduate student, I remember seeing only two genera of ascomycetes under the microscope: Aspergillus and Penicillium. However, there is another genus that is commonly used in biology classes, Sordaria, the dung fungi, whose most popular species is Sordaria fimicola, which I decided to call the lab dung fungus.

As its name suggest, the lab dung fungus is found growing on dung, more specifically on dung of herbivorous mammals. For a long time, it was thought that this species required dung to complete its life cycle. After growing on dung, the lab dung fungus releases its spores in the environment, they adhere to the surface of plants and are ingested by grazing mammals, restarting the cycle. However, it is now known that this species can grow and reproduce on plant matter without requiring dung, although more studies are needed to understand how the presence or absence of dung affects its fitness.

Fruiting bodies (perithecia) of Sordaria fimicola growing on dead leaf tissue of the grass Bromus tectorum. Credits to Newcombe et al. (2016).*

During most of its life, the lab dung fungus exists, just like other fungi, solely as a network of hyphae, the mycelium, growing inside the medium on which it feeds, in this case decaying plant matter, especially in dung. These hyphae are haploid (n), meaning that they have only one copy of each chromosome. When two hyphae touch, they can fuse and create a cell with two nuclei, the dykarion, each nucleus coming from one of the original hyphae. The dikaryotic cells divide through mitosis without fusing their nuclei, originating a set of dikaryotic hyphae that form a fruiting body, the perithecium, that grows inside the mycelium of haploid hyphae.

A bursted perithecium with released asci. Photo by Carmelita Levin.**

The perithecium is kind of pear-shaped and, inside of it, some dikaryotic cells allow their nuclei to fuse into a single, diploid nucleus, which now has two chromosomes of each type (2n), one from each parent hypha back then when the haploid hyphae meet. This newly formed diploid cell is a zygote but instead of growing into diploid hyphae by mitosis, it immediately undergoes meiosis to originate once again a set of haploid nuclei. The four resulting nuclei from meiosis each one undergoes mitosis, resulting in eight final nuclei, which remain lined up in the elongated cell. The cell then divides into eight individuals cells, each with one of the nucleus, and they turn into spores, ascospores, and remain inside an elongated sac, the ascus. When the ascospores are mature, they are released in the environment and can germinate to create a new set of haploid hyphae.

Lineages of the lab dung fungus found in nature often have very dark ascospores and this is called the wild type. However, one laboratory lineage has lighter, often gray ascospores, and is called the tan type. The color of the spore is determined by a single gene in one of the chromosomes. Thus, if you cross the wild and the tan types, the ascus of the hybrid will have four dark and four light spores, and this is how the lab dung fungus becomes a good species to understand meiosis and chromosome crossover in biology classes.

Lab dung fungus in the lab, growing in a Petri dish. Photo by Wikimedia user Ninjatacoshell.***

Before meiosis occurs, all chromosomes in a cell are duplicated, resulting in cell with four chromosomes of each type (4n) of which two are from one parent and two are from the other. When the nucleus divides for the first time, each daughter cell will be a special case of 2n, in which the two copies of each chromosome are originally from the same parent. In the lab dung fungus, considering the chromosome with the color gene, this would create a pattern like (AA)(AA) in these two nuclei. After the second division of meiosis, the pattern becomes (A)(A)(A)(A) and, after the mitosis that leads to the eight final spores, (A)(A)(A)(A)(A)(A)(A)(A).

Asci of a hybrid showing several combinations of dark and light ascospores. Extracted from https://www.fishersci.com/.

However, if crossover occurs, one pair of chromosomes from different parents exchange pieces with each other, while the other pair remains unaffected. As a result, they exchange the gene responsible for the color and the final product, instead of being 4 of one color followed by 4 of another (4:4 patterns), shows a 2:4:2 or a 2:2:2:2 pattern.

Resulting arrangement of the ascospores in the asci when chromosome crossover occurs (below) or not (above). Extracted and adapted from http://facweb.furman.edu/.

Sometimes other weird patterns appear as well, such as 2:1:1:1:1:2 patterns, but I guess this happens because of some mechanical action where one spore can roll over another and end up outside of its original position inside the ascus, perhaps caused when they are squeezed out of the perithecium. Really stranged patterns are those in which there are not 4 spores of each color, which include very rare instances of 6:2 or 5:3 patterns, and those are explained as the result of errorSs during chromosome replication.

Unusual 2:1:1:1:1:2 pattern probably caused because the two central ascospores were swapped because of pressure applied to the asci, so that the original pattern was 2:2:2:2 as expected when crossover occurs. Photo by Wikimedia user Ninjatacoshell.***

Isn’t the lab dung fungus indeed a very cool model to use in classes? I’m sad that I haven’t had the opportunity to see this in my genetics or microbiology classes. If you studied biology, were you lucky enough to see this? Let us know!

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References:

Dotson J (2019) Life cycle of Sordaria Fimicola. Sciencing. Available at < https://sciencing.com/life-cycle-sordaria-fimicola-6909851.html >. Acccess on 6 August 2020.

Kitani Y, Olive LS, E-Ani AS (1961) Transreplication and Crossing Over in Sordaria fimicola. Science 134: 668-669. https://doi.org/10.1126/science.134.3480.668

Newcombe G, Campbell J, Griffith D, Baynes M, Launchbaugh K, Pendleton R (2016) Revisiting the Life Cycle of Dung Fungi, Including Sordaria fimicola. PLoS ONE 11(2): e0147425. https://doi.org/10.1371/journal.pone.0147425

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New Species: July 2020

by Piter Kehoma Boll

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.

Bacteria

Gordonia mangrovi is a new actinobacterium from mangrove soil in China. Credits to Xie et al. (2020).*
Craterlacuibacter sinensis is a new proteobacterium from a crater lake in China. Credits to Liu et al. (2020).*

SARs

Cryptists

Chondria tumulosa is a new red alga from Hawaii. Credits to Sherwood et al. (2020).*

Plants

Bredia hispida is a new melastome from China. Credits to Dai et al. (2020).*
Beautiful conidia of Spegazzinia musae, a new didymospheriacean fungus from Thailand. Credits to Samarakoon et al. (2020).*

Amoebozoans

Fungi

Sidera parallela is a new crust fungus from China. Photo by Bao-Kai Cui.*

Poriferans

Advhena magnifica is a new hexactinellid from the North Pacific. Credits to Castello-Branco et al. (2020).*

Cnidarians

Enteromyxum caesio is a new myxosporean parasitizing the fish Caesio cuning. Credits to Freeman et al. (2020).*

Rotiferans

Flatworms

Nemerteans

Eggs (A), juvenile (B) and adult (C) of Auriculella gagneorum, a new land snail from Hawaii. Credits to Yeung et al. (2020).*

Mollusks

Loimia borealis is a new terebellid from Chinese waters. Credits to Wang et al. (2020).*

Annelids

Bryozoans

Nematomorphs

Nematodes

Tardigrades

Chelicerates

Myriapods

Crustaceans

Heterochelamon huidongense is a new freshwater crab from southern China. Credits to Wang et al. (2020).*

Hexapods

Atrococcus rushuiensis is a new scale insect from China. Credits to Zhang et al. (2020).*
Teleopsis neglecta is a new stalk-eyed fly from Sri Lanka. Photo by Amila P Sumanapala.**

Echinoderms

Tunicates

Chondrichthyans

Lucifuga gibarensis is a new cave fish from Cuba. Credits to Hernández et al. (2020).*

Actinopterygians

Amphibians

Mammals

Lycodon cathaya is a new snake from China. Credits to Wang et al. (2020).*

Reptiles

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