Life in marine driftwood: The case of driftwood specialist talitrids

Driftwood in the sea – either floating or stranded on beaches – is a common feature particularly in temperate regions. Large quantities of driftwood, termed driftwood depositories, may collect at the mouth of small streams associated with marshes and have been present for some 120 millennia – since the origin of flowering plants.

Once marine driftwood begins to decay, it undergoes a specific succession. Firstly, it is colonized by salt tolerant, wood degrading fungi and bacteria, along with a few invertebrates able to digest wood by producing native wood degrading enzymes. The latter include gribbles (isopods) and chelurid amphipods.

Driftwood hoppers (talitrids), as well as isopods, chilopods, insect larvae, some ants and termites, comprize the secondary colonizers. They are all characterized by their inability to utilize driftwood directly. Instead, they rely on symbiotic microflora for digestive purposes.

Within all talitrids, the driftwood hoppers count as few as seven species, most likely because they are extremely difficult to locate and, therefore, discover and describe. Apart from living in tiny burrows, they measure between 13 and <6 mm, which makes the latter the smallest known talitrid.

Having reviewed the driftwood specialized talitrids, Dr. David Wildish of the St. Andrews Biological Station, Canada, concludes that all seven known species demonstrate dwarfism based on slow metabolism and growth. Their sexual development begins earlier compared to faster growing related species. All of them are also characterized with reduced eye size and absence of dorsal pigment patterns.

In his review article published in the open access journal Zoosystematics and Evolution, the scientist confirms that dwarfism in driftwood hoppers has evolved due to poor diet, in turn resulting in slowed metabolism and growth. A further adaptive challenge is the empty gribble burrow size occupied by talitrids (burrow diameter between 0.6 to 5 mm) with the smaller ones being more widespread. Larger talitrids can only complete their life cycle in the larger burrows.

“The size gradient in gribble burrow diameter provides a satisfactory explanation for serial dwarfism within the driftwood talitrids and is why each species becomes successively smaller,” explains the researcher.

Responsibility for first establishing the driftwood talitrid ecological grouping was made during graduate studies by David Wildish, London University, U.K., and Laura Pavesi, University of Rome, Italy. The two criteria for inclusion of a talitrid in the driftwood grouping was: behavioral fidelity to the occupied driftwood and that the food source was solely rotting driftwood (see references).

The larger talitrid family are small/medium in body length (< 30 mm) crustaceans with more than 400 species described in the world list. Ecological groupings within the family include marine/estuarine supralittoral wrack generalists, sand-burrowing, marsh-living and driftwood specialists. A few freshwater and many terrestrial species are also known.

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Original source:

Wildish DJ (2017) Evolutionary ecology of driftwood talitrids: a review. Zoosystematics and Evolution 93(2): 353-361. https://doi.org/10.3897/zse.93.12582

How bears bulk up ahead of the summer: A study into the Asiatic black bear’s spring diet

Much like gym enthusiasts, every year Asiatic black bears seem to be on the lookout for protein-rich food ahead of the summer, so that they can bulk up on lean muscle mass in place of the fat tissue formed last year prior to hibernation. This was concluded in a study by Dr. Shino Furusaka, Tokyo University of Agriculture and Technology and his team, based on direct observations on bears living across an area of about 60 km2 in Japan. The study is published in the open access journal ZooKeys.

In order to determine the bears’ food preferences and habits, the scientists followed a large number of animals in the Ashio area of the Ashio-Nikko Mountains in Japan from April to July in both 2013 and 2014. To avoid unnecessary intrusion, they stayed at a distance of at least 200 metres using video cameras with telescopic lenses to document the sightings. Having documented the plant species the bears consumed, the researchers studied their nutritional content and made conclusions about the nutrients needed for the species after hibernation.

While heavily dependent on food availability, generally the bears were noted to prefer food which is high in protein, but poor in fibre — likely because their stomachs and intestines were unable to efficiently digest the latter. Furthermore, the protein-rich diet ensures that the muscle mass is rebuilt to replace the lost winter fat.

Interestingly, the bears were observed to change their food preferences as spring progressed and that seemed to be linked to the shifts in the nutritional value of the available food.

Starting with their observations at the beginning of April, the scientists did not record any feeding behaviour until the end of the month. As leaf flush was yet to occur, the animals were active and feeding on overwintered grass. However, in early May, the bears began consuming newly emerged leaves, grass and, later in the month, they added flowers to their menu.

A shift in behaviour occurred in the following months. In June and July, the bears were seen to feed mainly on ants, with a small portion of their food intake consisting of grasses, sika deer carcasses and bees. Curiously, when the scientists looked into the nutritional content of the same plants which the animals sought only a few weeks ago, they found out that now they were significantly poorer in protein and richer in fibre.

Another finding showed that the calories in the different items were not related to the choice of food which likely proves that the key factor is none other than the amount of protein, provided that the fibre value is low enough for good digestibility.

Understanding the food preferences and habits of animals, as well as the reasons behind them, is essential for the development and revision of habitat management plans. However, previous knowledge of the feeding behaviour of Asiatic black bears has been based solely on faecal analyses which has not provided sufficient details on which nutritional factors influence the use of particular foods.

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Original source:

Furusaka S, Kozakai C, Nemoto Y, Umemura Y, Naganuma T, Yamazaki K, Koike S (2017) The selection by the Asiatic black bear (Ursus thibetanus) of spring plant food items according to their nutritional values. ZooKeys 672: 121-133. https://doi.org/10.3897/zookeys.672.10078

Bee species with little known nesting-behavior observed to use plastic instead of leaves

Little is known about the nesting activities of some lineages of megachiline bees. Dr. Sarah Gess, affiliated with both Albany Museum and Rhodes University, South Africa, and Peter Roosenschoon, Conservation Officer at the Dubai Desert Conservation Reserve, United Arab Emirates, made use of their earlier observations gathered during a survey on flower visitation in the spring of 2015, to fill some gaps in the knowledge of of three species from such lineages.

Among their findings, published in the open access Journal of Hymenoptera Research, is a curious instance of a bee attempting to build brood cells using green pieces of plastic. Having examined two nests of the leafcutter bee species Megachile (Eurymella) patellimana, they report that one of the females nested in burrows in compacted sandy ground beneath a plant, and the other – in the banks of an irrigation furrow.

11290_Nest of P. grandiceps after emergence of imagines, visible trapped between their natal nest and a nest of Megachile maxillosa

However, while the former was seen carrying a freshly cut leaf, the latter seemed to have discovered a curious substitute in the form of green plastic. Later on, upon checking the nest, the researchers found that the phenomenon they had observed was no isolated incident – at least six identical pieces of narrow, tough, green plastic were grouped together in an apparent attempt to construct a cell. It turns out that the bee had been deliberately cutting off approximately 10-milimetre-long pieces with its large and strong toothed mandibles, before bringing them back to the nest.

“Although perhaps incidentally collected, the novel use of plastics in the nests of bees could reflect ecologically adaptive traits necessary for survival in an increasingly human-dominated environment,” the authors quote an earlier study.

The two studied mason bee species (Megachile (Maximegachile) maxillosa and Pseudoheriades grandiceps) were seen to construct their nests using a mixture of resin and sand in pre-existing cavities, such as trap-nests, above the ground. The researchers note that resin is a common nest-building material among numerous species of mason bees, also known as resin bees. Previously, it has been suggested that apart from making the nest waterproof, the plant secretions may contain substances that fend off parasites.

The authors’ earlier paper exploring the flower visitation by bees and wasps in the Dubai Desert Conservation Reserve is also published in the open-access Journal of Hymenoptera Research.

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Original source:

Gess SK, Roosenschoon PA (2017) Notes on the nesting of three species of Megachilinae in the Dubai Desert Conservation Reserve, UAE. Journal of Hymenoptera Research 54: 43-56. https://doi.org/10.3897/jhr.54.11290

Exceptional reproductive biology in extremely restricted critically endangered Nimba toad

The critically endangered Nimba toad is long known for its exceptional reproductive biology. The females of this unique species give live birth to fully developed juveniles, having for nine months continuously provided nutrition to the foetuses in the womb (matrotrophy). While live birth (viviparity) among frogs and toads is rather an exception than a common characteristic, matrotrophy, in place of alternatives such as the foetus being fed with yolk, unfertilized eggs, or smaller siblings, is what makes the Nimba toad one of a kind.

However, more than 40 years of research had not been comprehensively, accessibly and completely summarised. The gap has recently been filled with a new paper, published in the open access journal Zoosystematics and Evolution by German scientists Drs. Laura Sandberger-Loua and Mark-Oliver Rödel, both affiliated with Museum für Naturkunde, Berlin, and Dr. Hendrik Müller, Friedrich-Schiller-Universität Jena.

Studying the phenomenon, the scientists went through the literature published over four decades to gather the scattered details. They have also discussed the relationship between the toad’s reproductive biology and its specific habitat of merely 4 km² of high altitude grasslands located at a minimum of 1,200 m in the Nimba mountains, West Africa.

The climate of the area is characterised by a rainy season lasting from April to October and a dry season from November to February/March. These seasons are found to determine the activity of the Nimba toads. The amphibians are only active during the rainy season, when they give birth to their young, mate, and then find shelter underground, where they stay dormant during the dry season.

10489_ZSE_blogVisibly females can be distinguished from male Nimba toads by their differing cloaca and often larger size, compared to the males. Also, males show darker backs and, during most of their adult life, nuptial pads on their thumbs, which look like spiky swellings. This secondary sex characteristic, in its seasonal change linked to spermatogenesis, is used by the males to grasp tightly the female while mating.

In this species mating occurs without a copulatory organ. Instead, the sperm is transferred through connection of the cloacae, where the male’s swells and encloses the female’s cloaca. Furthermore, Nimba toads have a unique behavioural repertoire. Males crouch on their front legs and as soon as the female moves, follow her and grab her tightly in the groin. Due to the spiky nuptial pads, the males often injure their partner.

10489_ZSE_Image 3Giving birth in Nimba toads may take over two days, depending on the number of offspring, which can be up to 12 in older females – far fewer than the hundreds of eggs in most toad species. While giving birth, a female assumes a unique “birthing posture” to compensate for the lack of enough muscle power to expel juveniles. By the time the juveniles are ready to be born, they have already taken up nearly all the space in their mother’s body. The scientists conclude that the offspring play an active role in the process, as a juvenile toad’s death midway in the oviduct leads to the mother dying of sepsis.

Living exclusively in the Nimba mountains, and being listed as Critically Endangered, according to the IUCN, the studied toad is only one of the species restricted to the high altitude grasslands, which led to the declaration of the Nimba mountains as a World Heritage Site by UNESCO. Separated from other mountains, its inhabitants are isolated from external contacts, thus presumably leading to their evolutionary separation from related species. Furthermore, the toad’s unique reproductive biology is probably the result of this isolation, argue the authors.

In conclusion, the authors suggest that “it is likely that the harsh unpredictable environment and scarcity of open water promoted viviparity in Nimba toads, or supported the survival of this unique reproductive mode in these special and isolated conditions. Considering their complex life cycle, in which reproductive and seasonal cycles are tightly linked, understanding and protecting the Nimba toad’s threatened environment is of utmost importance.”

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Original source:

Sandberger-Loua L, Müller H, Rödel M-O (2017) A review of the reproductive biology of the only known matrotrophic viviparous anuran, the West African Nimba toad, Nimbaphrynoides occidentalis. Zoosystematics and Evolution 93(1): 105-133. https://doi.org/10.3897/zse.93.10489

Living together in mud: New bivalve species dwelling on a sea cucumber discovered in Japan

Most bivalves live in sand or mud or attached to rock surface. However, a new bivalve species described from Japan lives on a sea cucumber.

Ryutaro Goto, postdoctoral fellow in Museum of Zoology and Department of Ecology and Evolutionary Biology, University of Michigan, and Hiroshi Ishikawa, amateur malacologist in Japan, have their paper, describing the new species, published in the open access journal ZooKeys.

The new species, named Borniopsis mortoni(Galeommatoidea), was discovered in mudflats at the mouth of the Souzu River, southwestern Shikoku Island, Japan.

This bivalve has tiny brownish shells (up to 4.1 mm in length). The species lives attached by both its foot and byssal threads to the body surface of the earthworm-like sea cucumberPatinapta ooplax (Synaptidae). Individuals of B. mortoni are often found on the same host, yet sometimes there could be more than 10 individuals existing side-by-side.image_3_hishikawa

The new species is dedicated to a famous British malacologist Brian Morton, emeritus professor of University of Hong Kong. He has described many interesting Pseudopythina species from mudflats in Hong Kong, now assigned to the genus Borniopsis.

Host sea cucumbers burrow in mudflats. Most likely, the B. mortoni bivalve uses the host burrows as shelter from predators.

The new species is one of the smallest species in this genus. With the burrow of the host sea cucumber being very narrow, the small body size of B. mortoni is probably a corresponding adaptation.

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Original source:

Goto R, Ishikawa H (2016) Borniopsis mortoni sp. n. (Heterodonta, Galeommatoidea, Galeommatidae sensu lato), a new bivalve commensal with a synaptid sea cucumber from Japan. ZooKeys 615: 33-45. doi: 10.3897/zookeys.615.8125

The first long-horned beetle giving birth to live young discovered in Borneo

A remarkably high diversity of the wingless long-horned beetles in the mountains of northern Borneo is reported by three Czech researchers from the Palacký University, Olomouc, Czech Republic. Apart from the genera and species new to science, the entomologists report the first case of reproduction by live birth in this rarely collected group of beetles. The study was published in the open access journal ZooKeys.

Generally, insects are oviparous, which means that their females lay eggs and the embryonic development occurs outside the female’s body. On the other hand, ovoviviparous species retain their eggs in their genital tracts until the larvae are ready to hatch. Such mode of reproduction is a relatively rare phenomenon in insects and even rarer within beetles, where it has been reported for a few unrelated families only.

The long-horned beetles are a family, called Cerambycidae, comprising about 35,000 known species and forming one of the largest beetle groups.

“We studied the diversity of the rarely collected wingless long-horned beetles from Borneo, which is one of the major biodiversity hotspots in the world,” says main author and PhD student Radim Gabriš. “The mountains of northern Borneo, in particular, host a large number of endemic organisms.”

The scientists focused on the group which nobody had studied in detail for more than 60 years. They found surprisingly high morphological diversity in this lineage, which resulted in the descriptions of three genera and four species new to science.

“During a dissection of female genitalia in specimens belonging to the one of the newly described genera, named Borneostyrax, we found out that two females contained large larvae inside their bodies,” recalls Radim Gabriš. “This phenomenon have been known in a few lineages of the related leaf beetles, but this is the first case for the long-horned beetles.”

However, according to the authors, the modes of reproduction remain unknown for many beetle lineages besides Cerambycidae, so the ovoviviparity might be, in fact, much more common. Further detailed studies are needed for better understanding of the reproductive strategy in this group.

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Original source:

Gabriš R, Kundrata R, Trnka F (2016) Review of Dolichostyrax Aurivillius (Cerambycidae,Lamiinae) in Borneo, with descriptions of three new genera and the first case of (ovo)viviparity in the long-horned beetles. ZooKeys 587: 49-75. doi: 10.3897/zookeys.587.7961