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Otter update!

12/9/2014

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Our recent camera trapping efforts along Durham’s River Wear have been rewarded with some lovely pictures of local otters. 
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We first photographed the otters on our camera trap back in April, but these new images provide further evidence that they have an established local population. Otter populations across England suffered dramatic declines between the 1950’s and 1970’s due to increases in persecution and pesticides washing into waterways. Since the withdrawal of organo-chlorine pesticides, otter populations have been steadily increasing across the UK.  As an apex predator in English riverine environments, their presence here in Durham indicates that we have a healthy river system. This is encouraging news, not only for this threatened species, but for all of our local biodiversity.

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We also managed to capture a couple of Durham’s less salubrious characters on camera, including plenty of pictures of our local rat population (almost 500 pictures in one week alone!) and a couple of an American mink. American mink and European otters are very similar species, both semi-aquatic in nature and belonging to the same guild of mustelids. These species are sometimes mistaken for each other but you can see in the picture below that mink, despite being a similar shape to otters, are much smaller, have much darker, almost black fur and a fluffy tail.  Mink are an introduced species here in the UK, becoming established in the wild in the 1950’s due to a combination of purposeful releases and escapes from fur farms. Voracious carnivores, mink have been widely implicated in the population declines of water voles, as mink are small enough to follow their prey down its burrow. Recently, however, competition from the recovering otter populations seems to have caused a decline in mink populations. Hopefully the disturbance of mink will allow for the natural recovery of local water vole populations.

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Stayed tuned for more updates from our riverside camera trap. 
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the bats of durham university estate

7/9/2014

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Bats: a success under threat

With around 1200 species recorded worldwide, approximately one quarter of all known mammals are bats – only the rodents are more speciose. Bats occur almost everywhere on land, and are present on all continents with the exception of Antarctica.

Bats belong to the order Chiroptera, meaning ‘hand-wing’, which is split into the sub-orders Megachiroptera - the Old World fruit bats - and Microchiroptera. All seventeen resident British species are Microchiropterans. Two - the Greater horseshoe Rhinolophus ferrumequinum and the Lesser horseshoe R. hipposideros - belong to the family Rhinolophidae, and the remainder belong to Vespertilionidae; which is the largest mammalian family after Muridae (the Old World rats and mice). Yet, despite their evolutionary success, an estimated 15 percent of all bat species worldwide are now threatened with extinction by habitat loss, persecution and disease; and in the UK, all native species require protection from both national and international legislation.

Northern extremes

Being a small insectivorous mammal, living in a temperate climate has its drawbacks. Firstly, food supply is seasonal; secondly, being so small, much body heat is lost to the surrounding cooler air. Our bats overcome this by entering periods of torpor and hibernation in order to conserve energy. However, this strategy has its limits and there still exists a gradual loss in species diversity with increasing latitude. For example, in Devon, in the south-west of the country, sixteen species have been recorded (1); whilst up here in Durham, eleven species have been recorded – one of which remains unverified, and only eight of which are known to breed (2). Nevertheless, this figure may come as a surprise to many, especially those who are not even aware that bats are around us – sometimes quite literally!

Detecting bats

Bats are notoriously difficult to follow and to study, owing to their diminutive stature, nocturnal lifestyle and accomplished flying skills. Even here in the UK, with our rich history in the natural sciences, bats remain an enigma, and there is still very much to learn of their behaviour and ecology. However, there is an element of their anatomy and physiology that, in recent years, we have been able to exploit in order to begin scratching at the surface – this is the process of echolocation.

All Microchiropteran bats possess the ability to orientate by echolocation; which they achieve by emitting sounds through their mouths or noses and detecting the returning echo from solid objects. The average amplitude, duration and frequency of calls differ between species; so, in theory, we should be able to unmask a bat’s identity by measuring these parameters – if only it were always that simple! There is much overlap in the call parameters of closely-related species, and to add to the confusion, an individual will vary its call according to its foraging strategy and the habitat it is using. As a result, equipment and software has become increasingly sophisticated (and expensive) in order to assist a growing army of demanding bat hunters. However, detecting and identifying bats needn’t break the bank, and much can be achieved using a (relatively) inexpensive frequency division bat detector, an MP3 recorder and freely-available sound analysis software.

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Left:
My ‘batting’ equipment: a detector is essential; headphones, an MP3 recorder and sound analysis software are very useful; a cup of tea and a custard cream are optional.
The bats around our campus

The bat year begins with the end of hibernation, usually in March or April. On at least one evening in each month since March, I have taken a stroll around the perimeter of Great High Wood, stopping briefly at strategic points along the way, such as ponds, pasture and edge habitat. I listen to my detector over headphones and make notes of when and where I hear a bat. In the background, my MP3 recorder dutifully records everything that the detector picks up. Once indoors, the sound file can be downloaded to a computer and analysed using the sound analysis software. This is invaluable for verifying identifications made in the field, as well as for making sense of unidentified calls, and sometimes, for finding calls that were missed completely!

It is difficult to put an exact number on the total species I have recorded around campus – it could be as much as nine or as few as five. This is mainly because the echolocation calls of bats of the genus Myotis are very difficult to tease apart - even when viewed on a sonogram; and far more experienced ‘batters’ than I will often record them only as ‘Myotis sp.’. Below is a round-up of the species recorded, whether positively or potentially identified, along with both 'visual' and acoustic examples of their calls.

Myotis species

It is possible that I have recorded up to four Myotis species; but in reality, it is more likely to be two or three. The Whiskered Bat (Myotis mystacinus) and Natterer’s Bat (M. nattereri) are likely suspects, and, although strongly associated with water-bodies, Daubenton’s Bat (M. daubentonii) will also utilise the woodland. Brandt’s Bat (M. brandtii) is the fourth Myotis species recorded in County Durham, but is much rarer.
The sonogram and soundfile below are of the same echolocating Myotis individual, and are an example of how difficult it can be to separate the species of this genus by their calls alone; as certain parameters best fit one species, whilst others best fit another. What’s more, this recording was made in an open situation with no trees or other obstacles around, and the bat may have emitted a lower frequency range than it would have done in a cluttered environment. This is because it would not have needed to gain as much information about its immediate surroundings. It would take a braver (or more experienced) chiroptologist than myself to confidently identify this call to species-level!

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Noctule (Nyctalus noctula)

With a wingspan comparable to that of a blackbird (Turdus merula), the noctule is Britain’s largest bat. However, its body-size is far smaller, and even the largest of individuals weigh less than half that of the bird. The noctule is a fast and efficient flyer, utilising open spaces to hawk for its insect prey. It is the earliest species to take wing in the evening, and can be seen (or heard) even before the sun has met the horizon. I recorded this species in the pasture around Houghall Farm just to the south of Great High Wood.

There is a second species in Britain that belongs to the genus Nyctalus – this is Leisler’s Bat (N. leisleri). A large Leisler’s individual is about the size of a small noctule. It emits the same ‘chip-chop’ echolocation call as the noctule, but, on average, it is a higher frequency. Back in mid-May, I made two separate recordings of calls with parameters that fit Leisler’s Bat very well – one in Houghall Farm pastures, and another in the grasslands around the Mountjoy Centre.  However, since then, I have been reliably informed that this species is very scarce in County Durham, and that the calls were more likely to be those of Noctule. Nevertheless, I am going to remain ‘on the fence’ about this one, and record it simply as Nyctalus sp.
The sonogram and the sound file below are both snippets taken from the Mountjoy grasslands recording, and include a Common Pipistrelle (Pipistrellus pipistrellus) followed closely by the Nyctalus.

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Pipistrelles (Pipistrellus spp.)

I have recorded two pipistrelle species in and around Great High Wood – the Common Pipistrelle (Pipistrellus pipistrellus) and the Soprano Pipistrelle (P. pygmaeus). Aside from being our two commonest and most widespread species, these are also our two smallest; and, astonishingly, some individuals may weigh less than a two pence coin – or roughly the same as a Goldcrest (Regulus regulus; for those whose currency is birds). The two species are very similar and were identified as separate as recently as the 1990s; but with a little practice, they can be readily identified in the field by their echolocation calls – the peak frequency of the Common Pipistrelle being around 47kHz, and the Soprano around 55kHz (although there is some overlap around 50kHz).
The sonogram below shows an echolocating Soprano Pipistrelle (Pipistrellus pygmaeus), and demonstrates the classic ‘hockey stick’ shape of the pipistrelle’s call. There is a fair bit going on in the accompanying sound file; initially you may hear the feeding buzz – a ‘raspberry-like’ sound as the bat homes in on its prey. It is then joined by a second bat – also a Soprano Pipistrelle – and short scratchy or raspy sounds can be heard in the second half of the recording. These are social or contact calls made by the individuals communicating with each other, and are not used for echolocation.

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Brown Long-eared Bat (Plecotus auritus)

After the Common and Soprano Pipistrelles, the Brown Long-eared Bat is probably Britain’s next most abundant species. However, it has a very quiet echolocation call, often described as a 'light purring' or 'like the clicks of a Geiger counter', and a bat must be no more than a few metres away in order to be picked up by the detector. Consequently, despite its common status, I have recorded this species relatively infrequently.

The Brown Long-eared bat’s short, broad wings are suited to slow, manoeuvrable flight, and it sometimes hovers using its enormous ears to listen for its moving prey before picking it from the surface of vegetation. The species’ main prey is moths, with which it is locked in a coevolutionary ‘arms-race’. Many moths have evolved the ability to hear an approaching bat’s ultrasound, which allows them time to take evasive action. However, aside from having a very quiet echolocation call, the bat’s huge ears and relatively large eyes (compared to those of other bats) are adaptations to hunt using sight and sound; thus, avoiding detection.

I have recorded this species at the Mountjoy Pond, Houghall Pond and along the edge of Great High Wood itself. There is also a known roost within Hollingside House in Hollingside Lane - which they share with Common and Soprano Pipistrelles and an as yet unidentified Myotis species. I was privileged to witness some of these species emerge from the building when I joined Durham Bat Group for a dusk survey in July.
The recording below was made at Houghall Pond to the south of Great High Wood; where, although it must have passed just above my head, the bat remained unseen.

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By Stuart Brooker

Stuart is a MscR student with CEG studying spatial relationships between biodiversity and ecosystem services in urban environments
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Stu's top moths: week 12 - Common or garden moths

1/9/2014

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Each week we hear from Master's student Stuart Brooker who traps moths in the woodlands around Durham University. Stuart identifies, records and photographs the moths he traps, and provides CEG with a weekly update of his trapping efforts. 

Here is Stuart's week 12 report:

Following a rather promising first half of the ‘main’ mothing season, the second half is turning out to be a bit of a damp (and breezy) squib. There was no improvement in the weather for Week 12, and no improvement in the diversity and abundance of the catch. So, now seems like the perfect chance to show off some of the more commonly recorded species.

The Large Yellow Underwing (Noctua pronuba) is probably the most frequently recorded moth of my trapping sessions in the university woodlands so far. It is also the most frequently recorded species on the entire database for County Durham, and it is the second most frequently recorded species - after the Heart and Dart (Agrotis exclamationis) - in five years of trapping in my garden in Essex. This is undoubtedly among the most widespread and common of our moths, and familiarity with it certainly breeds contempt. But hold on a second ... before we tick off our 100th N. pronuba of the session and launch it unceremoniously back into the shroud of night, uttering under our breath “another Large Yellow Underwing; they’re so common", maybe we should pause, allow the moth to rest on our finger (if it will, they’re flighty at the best of times), or sit it in its pot. Let's ponder over it for a moment. 
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This a very variable species, with a number of colour morphs within a population; the individual we hold now may look different from the last, or the next. This is possibly an adaptation to predation pressure, whereby species that occur in high densities exhibit high colour polymorphism as an anti-searching image response. I’ll elaborate: predators may develop a search-image of commonly occurring prey. However, if the prey item exhibits a spread of different colour and pattern morphs throughout its population, the local predators will either need to build a catalogue of several explicit search-images, or make do with a general, and rather vague, search-image of its prey  – either way, being variable has its advantages. If this isn’t enough, behind its cryptic, and frankly, fairly dull facade, is more defensive weaponry – a flash of its bright, contrasting ‘yellow’ hindwings is designed to startle hunters on the prowl. What’s more, the moth we hold can detect foraging bats (Windmill et al., 2006) often before they can detect it, and is capable of navigating by the moon, the stars and the earth’s magnetic field (Baker & Mather, 1982).
So, now we’re ready to release our moth back into the night, perhaps instead we might utter “another Large Yellow Underwing; they're so common ... and they're a marvel of evolution”
The Mother of Pearl (Pleuroptya ruralis) has been one of the most commonly recorded of the micro-moths in the woodlands so far; and because of its size, it is one of the more obvious. The species is a good example of why the term ‘micro-moth’ is not always appropriate; with a wingspan of up to 40 mm, it is as large as many of the macro-moths, and superficially resembles those of the family Geometridae. Its larvae roll up the leaves of common nettle (Urtica dioica) and feed upon them from within; all the while, attached to a thread of silk. When threatened, the caterpillar dashes from its tubular domicile and dangles from its silken lifeline.

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Despite its common name, the Common Carpet (Epirrhoe alternata) has not been hugely numerous within the woodland, but instead has occurred in a steady stream of modest numbers; with the first generation visiting the trap throughout May, a break during June, and the second generation showing from the beginning of July up to the present.





The Canary-shouldered Thorn (Ennomos alniaria) is so named for its bright, canary-yellow thorax. The moth's speckled underwings resemble birch leaves as they turn yellow in the shortening days of Autumn; thus, providing camouflage for egg-laying females - whose offspring will feed on the tree next Summer. This is the fifth of the ‘thorns’ recorded in the woodland so far - the others being  Lunar Thorn (see Week 5), Early Thorn, Purple Thorn (both Week 9) and Dusky Thorn (Week 10).
This species is widely-distributed and frequent throughout Britain.
Stay tuned weekly for more 'Stu's Top Moths' or follow us on twitter for updates and photos of moths and other wildlife around Durham University!
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