Wednesday, 25 October 2017
25-10-2017 RACO DE OLLA, VALENCIA - BLACK TAILED GODWIT (Limosa limosa)
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The black-tailed godwit (Limosa limosa ) is a large, long-legged, long-billed shorebird first described by Carl Linnaeus in 1758. It is a member of the godwit genus, Limosa. There are four subspecies, all with orange head, neck and chest in breeding plumage and dull grey-brown winter coloration, and distinctive black and white wingbar at all times.
Its breeding range stretches from Iceland through Europe and areas of central Asia. Black-tailed godwits spend (the northern hemisphere) winter in areas as diverse as the Indian subcontinent, Australia, New Zealand, western Europe and west Africa. The species breeds in fens, lake edges, damp meadows, moorlands and bogs and uses estuaries, swamps and floods in (the northern hemisphere) winter; it is more likely to be found inland and on freshwater than the similar bar-tailed godwit. The world population is estimated to be 634,000 to 805,000 birds and is classified as Near Threatened. The black-tailed godwit is the national bird of the Netherlands.
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The black-tailed godwit is a large wader with long bill (7.5 to 12 cm (3.0 to 4.7 in) long), neck and legs. During the breeding season, the bill has a yellowish or orange-pink base and dark tip; the base is pink in winter. The legs are dark grey, brown or black. The sexes are similar, but in breeding plumage, they can be separated by the male's brighter, more extensive orange breast, neck and head. In winter, adult black-tailed godwits have a uniform brown-grey breast and upperparts (in contrast to the bar-tailed godwit's streaked back). Juveniles have a pale orange wash to the neck and breast.
In flight, its bold black and white wings and white rump can be seen readily. When on the ground it can be difficult to separate from the similar bar-tailed Godwit, but the black-tailed godwit's longer, straighter bill and longer legs are diagnostic. Black-tailed godwits are similar in body size and shape to bar-taileds, but stand taller.
It measures 42 cm (17 in) from bill to tail with a wingspan of 70–82 cm (28–32 in). Males weight around 280 g (9.9 oz) and females 340 g (12 oz). The female is around 5% larger than the male, with a bill 12–15% longer.
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The most common call is a strident weeka weeka weeka.
A study of black-tailed godwits in the Netherlands found a mortality rate of 37.6% in the first year of life, 32% in the second year, and 36.9% thereafter.
Black-tailed godwits have a discontinuous breeding range stretching from Iceland to the far east of Russia. Their breeding habitat is river valley fens, floods at the edges of large lakes, damp steppes, raised bogs and moorlands. An important proportion of the European population now uses secondary habitats: lowland wet grasslands, coastal grazing marshes, pastures, wet areas near fishponds or sewage works, and saline lagoons. Breeding can also take place in sugar beet, potato and rye fields in the Netherlands and Germany.
In spring, black-tailed godwits feed largely in grasslands, moving to muddy estuaries after breeding and for winter. On African wintering grounds, swamps, floods and irrigated paddy fields can attract flocks of birds. In India, inland pools, lakes and marshes are used, and occasionally brackish lakes, tidal creeks and estuaries.
Godwits from the Icelandic population winter mainly in the United Kingdom, Ireland, France and the Netherlands, though some fly on to Spain, Portugal and perhaps Morocco. Birds of the limosa subspecies from western Europe fly south to Morocco and then on to Senegal and Guinea-Bissau. Birds from the eastern European populations migrate to Tunisia and Algeria, then on to Mali or Chad. Young birds from the European populations stay on in Africa after their first winter and return to Europe at the age of two years. Asian black-tailed godwits winter in Australia, Taiwan, the Philippines, Indonesia, and Papua New Guinea.
Black-tailed godwits are much more likely to be found on inland wetlands than the more coastal bar-tailed godwit. They migrate in flocks to western Europe, Africa, south Asia and Australia. Although this species occurs in Ireland and Great Britain all year-round, they are not the same birds. The breeding birds depart in autumn, but are replaced in winter by the larger Icelandic race. These birds occasionally appear in the Aleutian Islands and, rarely, on the Atlantic coast of North America.
25-10-2017 DEVESA, VALENCIA - BLACK NECKED GREBE (Podiceps nigricollis ssp. nigricollis)
The black-necked grebe or eared grebe (Podiceps nigricollis ) is a member of the grebe family of water birds. It was described in 1831 by Christian Ludwig Brehm. There are currently three accepted subspecies, including the nominate subspecies. Its breeding plumage features a distinctive ochre-coloured plumage which extends behind its eye and over its ear coverts. The rest of the upper parts, including the head, neck, and breast, are coloured black to blackish brown. The flanks are tawny rufous to maroon-chestnut, and the abdomen is white. When in its non-breeding plumage, this bird has greyish-black upper parts, including the top of the head and a vertical stripe on the back of the neck. The flanks are also greyish-black. The rest of the body is a white or whitish colour. The juvenile has more brown in its darker areas. The subspecies californicus can be distinguished from the nominate by the former's usually longer bill. The other subspecies, P. n. gurneyi, can be differentiated by its greyer head and upper parts and by its smaller size. P. n. gurneyi can also be told apart by its lack of a non-breeding plumage. This species is present in parts of Africa, Eurasia, and the Americas.
The black-necked grebe uses multiple foraging techniques. Insects, which make up the majority of this bird's diet, are caught either on the surface of the water or when they are in flight. It occasionally practices foliage gleaning. This grebe dives to catch crustaceans, molluscs, tadpoles, and small frogs and fish. When moulting at saline lakes, this bird feeds mostly on brine shrimp. The black-necked grebe makes a floating cup nest on an open lake. The nest cup is covered with a disc. This nest is located both in colonies and by itself. During the breeding season, which varies depending on location, this species will lay one (sometimes two) clutch of three to four eggs. The number of eggs is sometimes larger due to conspecific brood parasitism. After a 21-day incubation period, the eggs hatch, and then the nest is deserted. After about 10 days, the parents split up the chicks between themselves. After this, the chicks become independent in about 10 days, and fledge in about three weeks.
Although it generally avoids flight, the black-necked grebe travels as far as 6,000 kilometres (3,700 mi) during migration. In addition, it becomes flightless for two months after completing a migration to reach an area where it can safely moult. During this moult, the grebe can double in weight. The migrations to reach these areas are dangerous, sometimes with thousands of grebe deaths. In spite of this, it is classified as a least concern species by the International Union for Conservation of Nature (IUCN). It is likely that this is the most numerous grebe in the world. There are potential threats to it, such as oil spills, but these are not likely to present a major risk to the overall population.
The black-necked grebe usually measures between 28 and 34 centimetres (11 and 13 in) in length and weighs 265 to 450 grams (9.3 to 15.9 oz). The bird has a wingspan range of 20.5-21.6 in (52-55 cm). The nominate subspecies in breeding plumage has the head, neck, breast, and upper parts coloured black to blackish brown, with the exception of the ochre-coloured fan of feathers extending behind the eye over the eye-coverts and sides of the nape. This eye is mostly red, with a narrow and paler yellow ring on the inner parts of the eye and an orange-yellow to pinkish-red orbital ring. The thin, upturned bill, on the other hand, is black, and is connected to the eye by a blackish line starting at the gape. Sometimes, the foreneck can be found to be mostly tinged brown. The upperwing is blackish to drab brown in colour and has a white patch formed by the secondaries and part of the inner primaries. The flanks are coloured tawny rufous to maroon-chestnut and have the occasional blackish fleck. The underwing and abdomen is white, with an exception to the former being the dark tertials and the mostly pale grey-brown outer primaries. The legs are a dark greenish grey. The sexes are similar.
In non-breeding plumage, the nominate has greyish-black upper parts, cap, nape, and hindneck, with the colour on the upper portion of the latter being contained in a vertical stripe. The dark colour of the cap reaches below the eye and can be seen, diffused, to the ear-coverts. Behind the ear-coverts on the sides of the neck, there are white ovals. The rest of the neck is grey to brownish-grey in colour and has white that varies in amount. The breast is white, and the abdomen is whitish. The flanks are coloured in a mix of blackish-grey with white flecks. The colour of the bill when not breeding differs from that of the breeding plumage, with the former being significantly more grey.
The juvenile black-necked grebe is similar to the non-breeding adult. There are differences, however, including the fact that the dark areas are usually more brownish in the juvenile, with less black. The lores are often tinged pale grey, with whitish marks behind the eye. On the sides of the head and upper neck, there is a buffy or tawny tinge. The chick is downy and has a blackish-grey head with stripes and spots that are white or pale buff-grey. The throat and foreneck are largely pale. The upper parts are mostly dark grey in colour, and the abdomen is white.
Tuesday, 24 October 2017
24-11-2017 MONTE CORONA, VALENCIA - SESAME LEAFROLLER (Antigastra catalaunalis)
Antigastra catalaunalis is a species of moth of the family Crambidae. The species was first described by Philogène Auguste Joseph Duponchel in 1833. It is endemic to tropical and subtropical areas (South Asia, Malay Archipelago, Africa), but is also found in other areas due to its migratory nature.
The wingspan is 19–22 mm. The forewings are pale yellow, veins and margins suffused with ferruginous, sometimes almost obscuring ground-colour; lines ferruginous, second strongly curved outwards on upper 2/3 ; small orbicular and discal spot fuscous ; cilia whitish, base dark fuscous. Hindwings are yellow whitish, ferruginous-tinged, termen more ferruginous ; a cloudy grey postmedian costal spot.
The larvae feed on snapdragons (Antirrhinum species), common toadflax (Linaria vulgaris), trumpetbush (Tecoma species), Scrophulariaceae and Pedaliaceae species.
24-11-2017 MONTE CORONA, VALENCIA - COMMON MAQUIS GRASSHOPPER (Pezotettix giornae)
Pezotettix giornae is a species of 'short-horned grasshoppers' belonging to the subfamily Pezotettiginae (similar to and previously placed in the Catantopinae.
This very little grasshopper is present in Southern Europe (and parts of Central Europe), North Africa and in the Near East.
This species inhabits meadows of lowlands, forest edges, xerotherm areas of plains and southern slopes of stony mountains.
The Common maquis grasshopper is non-toxic and generally doesn't pose a risk to human health.
The Common maquis grasshopper feeds on plants, usually without causing significant harm. However, it's important to take the situation seriously if their numbers begin to increase significantly.
The adult males grow up to 11–14 millimetres (0.43–0.55 in) long, while the females reach 12–18 millimetres (0.47–0.71 in) of length. The basic coloration of the body varies from light brown to greyish. The eyes are relatively large and the sides of thorax sometimes show a white or darker longitudinal stripe. The wings are scaly, oval, very short, reaching only the middle of the second rear segment, so they are unable to fly and resemble nymphs (brachyptery). Nymphs are usually green in the early stages.
This immature stages of this species develop in summer, passing through six instars. Adults can be encountered from June through November in the Mediterranean. They mate in autumn and in winter and often overwinter as adults. In this case they can be found by March.
Sunday, 22 October 2017
22-10-2017 PEGO MARJAL, ALICANTE - WHITE WAGTAIL (Motacilla alba)
The White wagtail is a slender bird with the characteristic long, constantly wagging tail of its genus. There are a number of other subspecies, some of which may have arisen because of partial geographical isolation, such as the resident British and Irish form, the pied wagtail M. a. yarrellii, which now also breeds in adjacent areas of the neighbouring European mainland. The Pied wagtail exchanges the grey colour of the nominate form with black (or very dark grey in females), but is otherwise identical in its behaviour. Other subspecies, the validity of some of which is questionable, differ in the colour of the wings, back, and head, or other features. Some rraces show sexual dimorphism during the breeding season. As many as six subspecies may be present in the wintering ground in India or Southeast Asia and here they can be difficult to distinguish.
The White wagtail (Motacilla alba) is a small insectivorous bird of the open country, often near habitation and water. It prefers bare areas for feeding, where it can see and pursue its prey. In urban areas, it has adapted to foraging on paved areas such as car parks. It is the national bird of Latvia and has been featured on the stamps of several countries.
White wagtails breed throughout Eurasia, only being absent in the Arctic. They also breed in the mountains of Morocco and western Alaska. These birds are residents in the milder parts of their range such as western Europe and the Mediterranean, but migratory in much of the rest of their range. Northern European breeders winter around the Mediterranean and in tropical and subtropical Africa, and Asiatic birds move to the Middle East, India, and Southeast Asia. Birds from the North American population also winter in tropical Asia. White wagtails occupy a wide range of habitats but are absent from deserts. They inhabit grasslands, seashores, rocky shorelines, sand beaches, tidepools, rivers, lakeshores, farmland, gardens, and parks. They are also often found in towns and villages.
The White wagtail is a slender bird with the characteristic long, constantly wagging tail of its genus. There are a number of other subspecies, some of which may have arisen because of partial geographical isolation, such as the resident British and Irish form, the pied wagtail M. a. yarrellii, which now also breeds in adjacent areas of the neighbouring European mainland. The Pied wagtail exchanges the grey colour of the nominate form with black (or very dark grey in females), but is otherwise identical in its behaviour. Other subspecies, the validity of some of which is questionable, differ in the colour of the wings, back, and head, or other features. Some rraces show sexual dimorphism during the breeding season. As many as six subspecies may be present in the wintering ground in India or Southeast Asia and here they can be difficult to distinguish.
White wagtails breed throughout Eurasia, only being absent in the Arctic. They also breed in the mountains of Morocco and western Alaska. These birds are residents in the milder parts of their range such as western Europe and the Mediterranean, but migratory in much of the rest of their range. Northern European breeders winter around the Mediterranean and in tropical and subtropical Africa, and Asiatic birds move to the Middle East, India, and Southeast Asia. Birds from the North American population also winter in tropical Asia. White wagtails occupy a wide range of habitats but are absent from deserts. They inhabit grasslands, seashores, rocky shorelines, sand beaches, tidepools, rivers, lakeshores, farmland, gardens, and parks. They are also often found in towns and villages.
22-10-2017 CAMI LES FONTS OLIVA MARJAL, VALENCIA - MALLARD (MALE) (Anas platyrhynchos)
The mallard (/ˈmælɑːrd, ˈmælərd/) or wild duck (Anas platyrhynchos) is a dabbling duck that breeds throughout the temperate and subtropical Americas, Eurasia, and North Africa. It has been introduced to New Zealand, Australia, Peru, Brazil, Uruguay, Argentina, Chile, Colombia, the Falkland Islands, and South Africa. This duck belongs to the subfamily Anatinae of the waterfowl family Anatidae. Males have green heads, while the females (hens or ducks) have mainly brown-speckled plumage. Both sexes have an area of white-bordered black or iridescent purple or blue feathers called a speculum on their wings; males especially tend to have blue speculum feathers. The mallard is 50–65 cm (20–26 in) long, of which the body makes up around two-thirds the length. The wingspan is 81–98 cm (32–39 in) and the bill is 4.4 to 6.1 cm (1.7 to 2.4 in) long. It is often slightly heavier than most other dabbling ducks, weighing 0.7–1.6 kg (1.5–3.5 lb). Mallards live in wetlands, eat water plants and small animals, and are social animals preferring to congregate in groups or flocks of varying sizes.
The female lays 8 to 13 creamy white to greenish-buff spotless eggs, on alternate days. Incubation takes 27 to 28 days and fledging takes 50 to 60 days. The ducklings are precocial and fully capable of swimming as soon as they hatch.
Male Mallards have a dark, iridescent-green head and bright yellow bill. The gray body is sandwiched between a brown breast and black rear. Females and juveniles are mottled brown with orange-and-brown bills. Both sexes have a white-bordered, blue “speculum” patch in the wing.
Unlike larger waterfowl such as the Tundra Swan, which mate for life, Mallard pairs only stay together for a season. Courtship and pair formation begin each fall and winter. Groups of males display for a hen with a variety of behaviors, including head and tail shaking, head-bobbing, dipping, and whistling.
The mallard is widely distributed across the Northern and Southern Hemispheres; in North America its range extends from southern and central Alaska to Mexico, the Hawaiian Islands, across the Palearctic, from Iceland and southern Greenland and parts of Morocco (North Africa) in the west, Scandinavia and Britain to the north, and to Siberia, Japan, and South Korea. Also in the east, it ranges to south-eastern and south-western Australia and New Zealand in the Southern hemisphere It is strongly migratory in the northern parts of its breeding range, and winters farther south.
The mallard inhabits a wide range of habitats and climates, from the Arctic tundra to subtropical regions. It is found in both fresh- and salt-water wetlands, including parks, small ponds, rivers, lakes and estuaries, as well as shallow inlets and open sea within sight of the coastline. Water depths of less than 0.9 metres (3.0 ft) are preferred, with birds avoiding areas more than a few metres deep. They are attracted to bodies of water with aquatic vegetation.
The female Mallard has between five and 14 light green eggs that she incubates for 30 days.
The ducklings are lead to water as soon as their soft, downy feathers are dry. ...
Most Mallard ducks live for one or two years, but some can live as long as 16 years!
Mallards swim with their tail held above the water.
22-10-2017 CAMI LES FONTS OLIVA, VALENCIA - MALLARD (FEMALE) (Anas platyrhynchos)
The Mallard, or wild duck (Anas platyrhynchos), is a familiar and widespread dabbling duck with a presence across temperate and subtropical regions of the Americas, Eurasia, and North Africa. It has also been introduced to parts of the Southern Hemisphere. The male is renowned for its iridescent green head and white collar, while the female sports a brown-speckled plumage. Both sexes boast a speculum—a patch of feathers with iridescent purple or blue hues bordered by white. The Mallard's length ranges from 50 to 65 cm, with a wingspan of 81 to 98 cm, and it typically weighs between 0.7 and 1.6 kg.
Males during the breeding season are unmistakable with their glossy green heads, white collars, and purple-tinged brown breasts. Females are mottled brown with buff cheeks and an eye-stripe. Both sexes have the distinctive speculum on their wings. The male's bill is yellowish-orange tipped with black, while the female's is darker, ranging from black to mottled orange and brown.
Mallards are found in a variety of wetlands, including parks, small ponds, rivers, lakes, and estuaries. They prefer water depths less than 0.9 meters and are drawn to areas with aquatic vegetation.
This species is distributed across the Northern and Southern Hemispheres, from Alaska to Mexico, the Hawaiian Islands, across the Palearctic, and down to southeastern and southwestern Australia and New Zealand.
Mallards are social birds that often form large flocks outside the breeding season. They are adaptable and can thrive in urban areas. The species is migratory in the northern parts of its range.
The female Mallard is known for its quintessential "quack," while the male's call is a quieter and deeper version of the female's. Vocalizations can vary by region, with urban ducks being louder than their rural counterparts.
Breeding pairs form in the fall, with the female laying 8 to 13 creamy white to greenish-buff eggs. Incubation lasts 27 to 28 days, and ducklings are precocial, swimming immediately after hatching.
Similar species include the American black duck, which is darker than the Mallard, and the mottled duck, which has slightly different coloration and lacks the white edge on the speculum.
Mallards are omnivorous, feeding on a variety of foods including seeds, plant matter, insects, crustaceans, and small animals. Their diet varies with the season and breeding cycle.
The Mallard is classified as Least Concern by the IUCN. However, it is considered invasive in some regions, where it can hybridize with and threaten local duck species.
22-10-2017 CAMI LES FONTS OLIVA, VALENCIA - GREYLAG GOOSE (Anser anser)
The Greylag Goose (Anser anser) is a large and robust member of the waterfowl family Anatidae, easily recognized by its mottled and barred grey and white plumage. It boasts an orange beak, pink legs, and a sizeable stature, measuring between 74 and 91 centimeters in length and weighing an average of 3.3 kilograms. This species is the progenitor of most domestic goose breeds and exhibits a wide distribution across Europe and Asia.
Adult Greylag Geese have a rotund body, a thick and long neck, and a large head and bill. Their legs and feet are pink, and their bill is orange or pink with a white or brown nail. The wingspan ranges from 147 to 180 centimeters. Males are typically larger than females, and the eastern subspecies rubirostris is larger than the nominate subspecies. The plumage is greyish brown with a darker head and paler underparts, with black spotting that varies among individuals. Juveniles can be identified by their lack of black speckling and greyish legs.
Greylag Geese breed in a variety of wetland habitats, including moorlands, marshes, lakes, and coastal islands. They prefer areas with dense vegetation for cover. In winter, they occupy semi-aquatic habitats such as estuaries, marshes, flooded fields, and agricultural lands.
The Greylag Goose has a Palearctic distribution, with the western subspecies breeding from Iceland to central Europe and the eastern subspecies from Romania to northeastern China. Northern populations often migrate southwards to spend the winter in warmer regions, while many populations are resident year-round.
Greylag Geese are known for their lifelong monogamous pair bonds. They are gregarious and form flocks, which provides safety in numbers. Family groups stay together, migrating southwards in autumn and separating the following year. They are herbivorous, feeding mainly on grasses, and can cause damage to agricultural crops.
The call of the Greylag Goose is a loud cackling, similar to that of domestic geese. They use various calls for different situations and can recognize individual geese by voice. Flocks produce a sound reminiscent of baying hounds.
Greylag Geese mate for life and nest on the ground among vegetation. They lay a clutch of three to five eggs, which the female incubates. Both parents defend and rear the young, who are precocial and leave the nest shortly after hatching.
The Greylag Goose can be confused with other grey geese of the genus Anser, but its larger size, bulkier body, and specific plumage pattern help distinguish it.
The diet consists mainly of grasses, but also includes grains, tubers, and occasionally small aquatic animals. They have adapted to feed on agricultural crops, which has led to conflicts with farmers.
The Greylag Goose is currently listed as Least Concern by the IUCN, indicating a stable and widespread population. However, some local populations may face threats from habitat loss and conflicts with agriculture.
22-10-2017 MONTE CORONA, VALENCIA - EUROPEAN MANTIS (MALE) (Mantis religiosa)
The European mantis (Mantis religiosa) is a large hemimetabolic insect in the family of the Mantidae ('mantids'), which is the largest family of the order Mantodea (mantises). Their common name praying mantis is derived from the distinctive posture of the first pair of legs that can be observed in animals in repose. It resembles a praying attitude. Both males and females have elongated bodies with two pairs of wings. The most striking features that all Mantodea share are a very mobile, triangular head with large compound eyes and their first pair of legs (the 'raptorial legs'), which is highly modified for the efficient capture and restraint of fast-moving or flying prey.
In Germany, M. religiosa is listed as Gefährdet on the German Red List on the basis of an assessment from 1998. It is not supposed to be caught or held as a pet. At a global level, it is assessed by the IUCN as least concern.
The great variation in the coloration of M. religiosa from different shades of yellow, brown, green, and sometimes black has been the cause of numerous hypotheses and studies for over 100 years. However, no generally accepted answer about reason, benefit, or mechanism of the coloration or the change of coloration has been found.
Di Cesnola observed in 1904 that green mantids were found on fresh green grass, whereas brown individuals seemed to prefer brown grass burned by the sun. When forced to change the location as to no longer match their coloration, almost all the ‘not matching’ animals were killed by predators such as birds. This indicates a camouflaging purpose of the coloration.
Przibram also observed in 1907 that a change in temperature can trigger a change in coloration: animals that hatched in a cold environment turned green after moulting when heat and sunlight were provided. Without the change in temperature and only a change in the color of the background, no change in coloration occurred. This finding contradicts with Di Cesnola, who claims to have observed the animals within the same time and location (and therefore the same temperature).
The sexual behavior of praying mantids in general is curious, so has received interest from scientists over the last century. The differences between the various species are well known.
In M. religiosa, courtship and mating are separated into two steps: Preliminary courtship begins with the first visual contact between the animals and ends with the first physical contact. Copulation begins with physical contact and ends when the spermatophore is deposited.
Only a few days after the final moult into adults, the animals begin to show interest in the opposite sex; this point is marked as the achievement of sexual maturity. Males have been observed to be most attracted to females during the middle of the day when the temperature is hottest. Theories are that the female pheromones are most volatile in the heat and that also the male, as a thermophilic insect, is most active.
Instead of just observing them, sexually mature males approach sexually mature females when they see them, but due to the physical superiority of the females, males of M. religiosa face certain challenges in doing so. When a female spots a male, she is very likely to attack and kill him (see also: Sexual cannibalism). Therefore, males can be observed to be very slow and cautious in their approach; after spotting a female, the male usually freezes and turns his head to look directly at her. Since the foveae in his eyes face directly forwards, he has the most accurate and detailed view of her and can watch every one of her moves. He then proceeds to approach her from behind. Males can be observed to stop as soon as the female turns her head or even moves. Mantids are very good at detecting moving structures, but are almost unable to see immobile objects. Using this ‘stop-and-go’ tactic, the male stalks closer to the female. This can often take several hours. Depending on the environment, males sometimes show a light ‘rocking’-behavior which is believed to imitate the leaves of surrounding plants to blend in with the background. Males doing this had no higher probability of being detected and attacked, which supports this hypothesis of concealment.
No mention of male or female courtship has been made in either the field or captivity. The male, in fact, does not win by display; he wins by the absence of display.Once the male is close enough to the female, he opens his wings a little to facilitate his jump on the female's back. As soon as he lands, he proceeds to hold on to her with his raptorial legs. His tibiae fit into a pair of grooves on either side of the female's mesothorax in front of her wing bases.When the male is in a secure position, copulation is initiated. The genitals, which are found on the end of the abdomen in both sexes, look quite different; the males possess a pair of asymmetrical claspers, while the females have an ovipositor. The ovipositor is rather short in comparison to other insects. It is covered in part by the edges of the last sternum. The abdomen of the male curves and twists in a 90° angle around the female's to insert the claspers between the ovipositor and the sternum. The abdomen of the male then contracts in a peristaltic manner. The animals can stay in this position for four to five hours before a spermatophore is deposited inside the female and the claspers are withdrawn. The male then lets go of the female to drop to the ground to get out of her reach for his own safety. After getting away about 50 cm, he stops and freezes for about four minutes before he leaves eventually. This behavior could be interpreted as necessary rest after the efforts of copulating in a safe distance from the female.
22-10-2017 MONTE CORONA, VALENCIA - WESTERN CONIFER SEED BUG (Leptoglossus occidentalis)
The western conifer seed bug (Leptoglossus occidentalis), sometimes abbreviated as WCSB, is a species of true bug (Hemiptera) in the family Coreidae. It is native to North America west of the Rocky Mountains (California to British Columbia, east to Idaho Minnesota and Nevada) but has in recent times expanded its range to eastern North America, to include Ontario, Québec, New Brunswick, Nova Scotia, Michigan, Maine, Pennsylvania, New York, Connecticut, Massachusetts, New Hampshire, Ohio, Indiana, and Wisconsin, and has become an accidental introduced species in parts of Europe and Argentina.
This species is a member of the insect family Coreidae, or leaf-footed bugs, which also includes the similar Leptoglossus phyllopus and Acanthocephala femorata, both known as the "Florida leaf-footed bug". Western conifer seed bugs are sometimes colloquially called stink bugs. While they do use a foul-smelling spray as a defense, they are not classified in the stink bug family Pentatomidae. In Chile, it has been confused with kissing bugs (Triatominae), causing unjustified alarm.
The average length is 16–20 millimetres (0.63–0.79 in) with males being smaller than females. They are able to fly, making a buzzing noise when airborne. Western conifer seed bugs are somewhat similar in appearance to the wheel bug Arilus cristatus and other Reduviidae (assassin bugs). These, being Cimicomorpha, are not very closely related to leaf-footed bugs as Heteroptera go; though both have a proboscis, but only the assassin bugs bite even if unprovoked, and L. occidentalis like its closest relatives can be most easily recognized by the expanded hindleg tibiae and by the alternating light and dark bands which run along the outer wing edges on the flaring sides of the abdomen.
Their primary defense is to emit an unpleasant-smelling alarm pheromone; however, if handled roughly they will stab with their proboscis, though they are hardly able to cause injury to humans as it is adapted only to suck plant sap and not, as in the assassin bugs, to inject venom.
In its native range, the western conifer seed bug feeds on the sap of developing conifer cones throughout its life, and its sap-sucking causes the developing seeds to wither and misdevelop. It is therefore considered a minor tree pest in North America, but becoming sometimes more harmful e.g. in conifer plantations. However, it is not monophagous and even adaptable enough to feed on angiosperms if it has to, though it seems to prefer resiniferous plants that are rich in terpenes. As these are produced by plants to deter herbivores, it might be that in evolving its ability to overcome these defenses, L. occidentalis actually became somewhat dependent on such compounds.[citation needed]
Its host plants in the native range include conifers such as Douglas-fir (Pseudotsuga menziesii), ponderosa pine (Pinus ponderosa), lodgepole pine (Pinus contorta), and white spruce (Picea glauca). Outside the native range, it is found on species such as eastern white pine (P. strobus) and red pine (P. resinosa) in eastern North America and Europe, and mountain pine (P. mugo), black pine (P. nigra), Scots pine (P. sylvestris) and pistachio (Pistacia vera) in Europe.
The eggs are laid in small groups on the needles or leaf stems of its host plants, and hatch in spring. The nymphs go through 5 instar stages before moulting into adults. In the United States, the species is univoltine, but in southern Europe, it completes two generations a year, and in tropical Mexico even three. In the northern parts of its range, these bugs start to move about widely by September or so to seek crevices for overwintering; they may become a nuisance in areas with extensive conifer woods, as they will sometimes enter houses in considerable numbers. They have the potential to become structural pests, as it has been found that they will sometimes pierce PEX tubing with their mouthparts, resulting in leakage.
Friday, 20 October 2017
20-10-2017 CAMI LES FONTS OLIVA, VALENCIA - LITTLE EGRET (Egretta garzetta)
The Little egret (Egretta garzetta) is small elegant heron in the family Ardeidae. As an aquatic bird, it feeds in shallow water and on land, consuming a variety of small creatures. At one time common in Western Europe, the Little heron was hunted extensively in the 19th century to provide plumes for the decoration of hats and became locally extinct in Northwestern Europe and scarce in the south. Around 1950, conservation laws were introduced in southern Europe to protect the species and their numbers began to increase.
The plumage of the Little egret is normally entirely white, although there are dark forms with largely bluish-grey plumage. In the breeding season, the adult has two long plumes on the nape that form a crest. These plumes are about 150 mm (6 in) and are pointed and very narrow. There are similar feathers on the breast, but the barbs are more widely spread.
The Little Egret is a small white heron with attractive white plumes on crest, back and chest, black legs and bill and yellow feet. It first appeared in the UK in significant numbers in 1989 and first bred in Dorset in 1996. Its arrival followed naturally from a range expansion into western and northern France in previous decades. It is now at home on numerous south coast sites, both as a breeding species and as a winter visitor.
With its yellow feet, which are used to flush prey when feeding in shallow water, the Little Egret is a distinctive member of the heron family.
Little Egrets first bred in Britain in 1996 and since then have successfully colonised much of southern Britain and Ireland. Most of the breeding colonies have been established within existing Grey Heron colonies, the two species nesting alongside one another.
The winter distribution is also currently restricted to the southern half of Britain & Ireland, despite the fact that young birds are known to move some distance from their natal site.
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