Conservation and nameless earthworms: Assessors in the dark?

Species that live exclusively in a single region are at a particular risk of extinction. However, for them to be protected, thorough assessments of the environmental impacts need to be performed.

There are more than 100 earthworm species living in the soil and dead wood of KwaZulu-Natal Province, South Africa. Most of them live exclusively in small regions in the province, which makes them extremely vulnerable.

To scientists Dr Adrian J. Armstrong, Ezemvelo KZN Wildlife, and Ms Thembeka Nxele, KwaZulu-Natal Museum, the problem is twofold. Firstly, they note that the expression “out of sight, out of mind” is very suitable for the case of the endemic earthworms in South Africa. Secondly, they point out that the lack of common names for these species is a stumbling block that hinders their inclusion in conservation assessments.

As a result, the researchers try to rectify this situation by assigning standardised English names to the endemic earthworms in KwaZulu-Natal. Their article is published in the open access journal African Invertebrates.

Scientific names are often intractable to non-specialists, and the lack of common names leaves environmental assessors in the dark when they need to figure out which earthworms may occur at a development site. In the meantime, it has been found that about 50% of the native vegetation in KwaZulu-Natal has already been removed as a result of infrastructure construction and the figure is rising.

“The indigenous earthworms generally don’t survive in developed areas,” say the authors.

For instance, the informal use of an English name (green giant wrinkled earthworm) for the species Microchaetus papillatus, has facilitated the inclusion of this species in environmental impact assessments in KwaZulu-Natal.

While the green giant wrinkled earthworm does occur in a relatively large and rapidly developing area in KwaZulu-Natal, other species live in smaller areas that have been urbanised even more.

The extinction of these earthworms is not only undesirable from the point of view of biodiversity advocates – the role of this group of soil organisms is impossible to replace fully with non-native earthworms. For example, some of the large indigenous earthworms (more than 1 m in length) burrow much deeper than the non-native species, thereby enriching and aerating the soil at greater depth.

The authors are hopeful that by giving the indigenous earthworms in KwaZulu-Natal common names, the threatened and endemic species will be conserved through inclusion in environmental impact assessments. Furthermore, they believe that earthworms could draw attention to the areas where they occur whenever a choice for new protected areas is to be made.

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Original source:

Armstrong AJ, Nxele TC (2017) English names of the megadrile earthworms (Oligochaeta) of KwaZulu-Natal. African Invertebrates 58(2): 11-20. https://doi.org/10.3897/AfrInvertebr.58.13226

New species of Brazilian copepod suggests ancient species diversification and distribution

A new species of groundwater copepod has been discovered in the rocky savannas of Brazil – an ecosystem suffering from heavy anthropogenic impact. Upon description, the tiny crustacean turned out to also represent a previously unknown genus. It is described by Dr. Paulo H. C. Corgosinho, Montes Claros State University, Brazil, and his team in the open access journal Zoosystematics and Evolution.

Prior to the discovery of the new species, named Eirinicaris antonioi, only one genus of its subfamily (Parastenocaridinae) had been recorded in the Neotropical region, which comes to show that related species had already spread across a huge range when the ancient supercontinent Gondwana split apart.

The new copepod measures about 0,300 mm and can be told apart by its morphological characteristics, including unusual sensorial structures at the rear part of the body, as well as unique sexual dimorphism.

The copepods of the family Parastenocarididae are adapted to life in groundwater, where they thrive between sand grains. These tiny creatures measure less than 1 mm, ranging between 0,200 and 0,400 mm in length. They can be found in various microbiotopes along rivers, lakes and human-made structures, such as dug or artesian wells. Alternatively, these copepods might be associated with mosses and other semi-terrestrial environments.

“This is the first species described from Goiás state, Central Brazil,” explain the authors. “With the discovery of this new species our knowledge about the geographical distribution of the copepod family Parastenocarididae is increased. Our project highlights the vast amounts of undiscovered biodiversity of the Brazilian rocky savannas, which are under high anthropogenic threat.”

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Original source:

Corgosinho PHC, Schizas NV, Previattelli D, Falavigna da Rocha CE, Santos-Silva EN (2017) A new genus of Parastenocarididae (Copepoda, Harpacticoida) from the Tocantins River basin (Goiás, Brazil), and a phylogenetic analysis of the Parastenocaridinae. Zoosystematics and Evolution 93(1): 167-187. https://doi.org/10.3897/zse.93.11602

American scientists discover the first Antarctic ground beetle

Fossilised forewings from two individuals, discovered on the Beardmore Glacier, revealed the first ground beetle known from the southernmost continent. It is also the second beetle for the Antarctic insect fauna with living descendants. The new species, which for now is also the sole representative of a new genus, is to be commonly known as Ball’s Antarctic Tundra Beetle. Scientists Dr Allan Ashworth, North Dakota State University, and Dr Terry Erwin, Smithsonian Institution, published their findings in the open access journal ZooKeys.10535_image-3

The insect fauna in Antarctica is so poor that today it consists of only three species of flightless midges, with one of them having been probably introduced from the subantarctic island of South Georgia. The absence of biodiversity is considered to be a result of lack of moisture, vegetation and low temperatures.

10535_image-2Following their study, the authors conclude that the beetle must have inhabited the sparsely-vegetated sand and gravel banks of a meltwater-fed stream that was once part of an outwash plain at the head of a fjord in the Transantarctic Mountains. Plants associated with the extinct beetle include southern beech, buttercup, moss mats, and cushion plants, all typical for a tundra ecosystem. The species may or may not have been able to fly.

The closest modern relatives to the extinct species live in South America, the Falkland Islands, South Georgia, Tasmania and Australia. Tracking the ancient lineage of this group of beetles, known as the carabid beetle tribe Trechini, confirms that they were once widely distributed in Gondwana, the supercontinent that used to unite what today we recognise as Antarctica, South America, Africa, Madagascar, Australia, the Arabian Peninsula and the Indian Subcontinent. Ball’s Antarctic Tundra Beetle is also an evidence that even after Gondwana broke apart, the tundra ecosystem persevered in Antarctica for millions of years.

“The conflicting signals both in anatomical attributes and biogeography, and in ecological setting as well, leave open the question of relationships, thus giving us no alternative but to flag the species represented by fossil evidence through erection of new genus status, hence drawing attention to it and the need for further paleontological studies in Antarctica,” speak of their discovery the authors.

The new Ball’s Antarctic Tundra Beetle is scientifically identified as Antarctotrechus balli, where the genus name (Antarctotrechus) refers to its being related to the tribe Trechini, and the species name (balli) honours distinct expert of ground beetles Dr. George E. Ball, who celebrated his 90th birthday on 26th September, 2016.

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Original source:

Ashworth AC, Erwin TL (2016) Antarctotrechus balli sp. n. (Carabidae, Trechini): the first ground beetle from Antarctica. ZooKeys 635: 109-122. https://doi.org/10.3897/zookeys.635.10535

People can simultaneously give a hand to endangered apes and stay at safe distance

Primates claim the highest proportion of endangered species among all mammals, according to the IUCN Red List. Yet, the substantial conservation interference from humans, which is already in place, could itself lead to even greater losses.

Plenty of studies have proven that while researchers and ecotourists raise vital for ape conservation knowledge and funds, it is actually human presence that compromises primates’ well-being due to extremely similar genetics and, thereby, easily transmittable diseases, ranging from common cold to human tuberculosis and Ebola fever.

In a paper published in the open access journal BioRisk, Rhiannon Schultz, Miami University, seeks the golden mean between giving ape species a hand and keeping safe distance. To showcase the impact human have on primates, the scientist makes example of the Mountain gorilla, an endangered species living in the montane forests of the Democratic Republic of Congo, Uganda and Rwanda.

Simply being in close proximity to primates, humans can easily transmit a wide range of diseases to the animals, including intestinal parasites, hepatitis, tuberculosis, Typhoid fever, Cholera, and Ebola fever. The transmission can occur as easily as having the two species breathing the same air, or the people leaving a banana peel behind.

Furthermore, threats to the gorilla species are also posed by the humans destroying the primates’ habitats. The result is overlapping populations, where a disease is much easier to transmit among the small gorilla populations. For example, normally an ill individual would be put under a ‘natural quarantine’, which is impossible when the habitat has already been reduced.

In the meantime, banning people, both tourists and scientists, from gorilla habitat is not an option, since knowledge about the populations’ dynamics is essential for the conservation of all primate species. On the other hand, ecotourism is what raises a great part of the resources need for conservation work. Income from gorilla trekking is enough to support the Ugandan Wildlife Authority, while also contributing a significant part to the country’s national budget.

The key, Rhiannon Schultz concludes, is to, firstly, promote understanding of the risk for interspecies disease transmission as a conservation threat, and then, improve on current protocols and regulations.

“It may be difficult to ask tourists to wear masks while visiting animals in the wild, and it may be expensive to maintain a veterinary program for wild populations and to improve healthcare systems for local people, but making these improvements could be the key to preventing disease transmission to not only Mountain gorillas but also to other apes,” sums up the scientist.

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Original source:

Schultz R (2016) Killer Conservation: the implications of disease on gorilla conservation.BioRisk 11: 1-11. doi: 10.3897/biorisk.11.9941

Tracing the ancestry of dung beetles

One of the largest and most important groups of dung beetles in the world evolved from a single common ancestor and relationships among the various lineages are now known, according to new research by an entomologist from Western Kentucky University.

The study by Dr T. Keith Philips, recently published in the open access journal ZooKeys, provides important insights into the evolution and diversity of these dung beetles, which make up about half of the world’s dung beetle fauna.

The two tribes studied, the onthophagines and oniticellines, evolved from a single common ancestor and are found worldwide, except for Antarctica. These dung beetles make up the vast majority of species and dung beetle biomass in many ecosystems, feeding on mammal dung.

Dung beetles are well known to many people because many species are colorful and active in the daytime. Additionally, many taxa have unusual behaviors, such as making and rolling balls of dung away from a dung pile. Often thought of as nature’s garbage collectors, the important ecosystem service offered by dung beetle helps recycle nutrients, reduces parasites, and can even help seeds germinate.

While the two tribes studied do not have species that create balls, they instead have evolved many other diverse behaviors. This includes species that do not feed on dung but specialize on fungi, carrion, and dead millipedes. Many species that evolved from the same common ancestor even live in close association with termites and ants, where they might be feeding on nest debris.

“This is one of the most important groups of dung beetles that finally has a hypothesis on how they evolved and diversified on earth,” Philips notes. “The evolutionary scenario can now be tested and refined in the future with more data.” Although relatively well known, this group still may have as many as 1,000 undiscovered species left for scientists to document.

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Original source:

Philips TK (2016) Phylogeny of the Oniticellini and Onthophagini dung beetles (Scarabaeidae, Scarabaeinae) from morphological evidence. ZooKeys 579: 9-57. doi: 10.3897/zookeys.579.6183.

Poorly known South African mountain endemic appears to be a very valuable keystone species

Mountain ecosystems are valuable providers of key resources including water. These ecosystems comprise diverse species, some of which appear to be especially important to the ecosystem’s functioning. In poorly studied mountain environments in biodiversity-rich countries, these keystone species can often be overlooked and undervalued.

Macowania is a group of yellow daisy shrubs occurring in the alpine-like regions of the Drakensberg and highlands of Ethiopia, Eritrea and Yemen. Doctoral student Joanne Bentley, University of Cape Town, studied the genetic relationships between the various Macowaniaspecies and relatives during her Masters degree studies. Her research led to the first collection of the poorly known species Macowania revoluta (known also as the Amathole Macowania) in about 40 years.

The story of Macowania revoluta is published in the open access journal PhytoKeys.

The Amathole Macowania appears to be an exceptionally important keystone species. This is because it forms one of the dominant members of the valuable mountain wetland communities and, thus, likely plays a very important role in wetland functioning and soil protection.

It appears to be somewhat tolerant of woody alien species and a valuable pioneer species protecting its native co-habitants. Plants like this one buffer more sensitive plants from sudden changes in environment (such as forestry, alien invasion and fire), and provide an opportunity for the ecosystem to ‘bounce back’.

113693Restricted to the Amathole mountains in the Eastern Cape Province, South Africa, the Amathole Macowania was first collected sometime before 1870 by the pioneer botanist Peter MacOwan, and was well documented until around 1949. After that, except for one record in 1976, the plant quietly disappeared.

“This was the first Macowania species that we found during our fieldtrip across the greater Drakensberg. We had combed several of the localities where it had been collected before; mostly from several decades ago, some from more than a century ago!” says Joanne Bentley. “We became increasingly doubtful about finding the plant, given the heavily transformed plantation landscape.”

“Ready to throw in the towel, we came across a peaty area on the margins of the forest and decided on one last investigation. We were lucky: it was growing prolifically! It was a very special moment.”

As it often happens, exciting discoveries come in bulk. Joanne’s discovery of the plant in July 2010 was followed by another record in October 2010, by the Curator of the Schonland Herbarium, Tony Dold. In 2014 at least three additional localities were recorded along the popular Amathole Hiking Trail by Dr Ralph Clark, Rhodes University. A further record was added in 2015 by Vathi Zikishe, South African National Biodiversity Institute. The verdict: this is a very localised but patchily abundant species, and an ecologically valuable component of the Amathole flora.

Listed as ‘Data Deficient’ in the Threated Plants List for South Africa, this string of modern records of the species also provided the first opportunity to get an idea of its ecology and abundance, as well as the first photographs.

“The practical value of this species in local land restoration projects still needs to be explored, but the opportunities are exciting,” says Dr Clark. “The discovery that this obscure endemic mountain plant is not only abundant, but is, in fact, fulfilling an extremely important ecological role, highlights the value of detailed mountain biodiversity research in southern Africa.”

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Original source

Clark VR, Bentley J, Dold AP, Zikishe V, Barker NP (2016) The rediscovery of the Great Winterberg endemic Lotononis harveyi B.-E.van Wyk after 147 years, and notes on the poorly known Amathole endemic Macowania revoluta Oliv. (southern Great Escarpment, South Africa). PhytoKeys 62: 1-13. doi: 10.3897/phytokeys.62.8348