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14. Table of Contents
Foreword . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . xvii
Preface . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . xix
1. AIR . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
Installing the Adobe Development Tools 2
Flash Professional CS5.5 2
Flash Builder 4.5 2
Installing the AIR Runtime on an Android Device 2
What Is in the AIR SDK 3
New ActionScript Libraries 4
Functionalities Not Yet Supported 5
AIR on the Desktop Versus AIR on Android 5
Mobile Flash Player 10.1 Versus AIR 2.6 on Android 6
2. Call Me, Text Me . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
Setting Up Your Device 8
Creating a Project 8
Using Flash Professional 8
Using Flash Builder 9
Creating the Application Descriptor 9
Using Flash Professional 9
Using Flash Builder 9
Writing the Code 10
Using Flash Professional 11
Using Flash Builder 12
Packaging Your Application As an APK File and Installing
It on the Device 12
Using Flash Professional 12
Using Flash Builder 13
Testing and Debugging 13
vii
15. Using Flash Professional 13
Using Flash Builder 14
Mobile Utility Applications 15
Launchpad 15
Device Central CS5 15
Package Assistant Pro 15
De MonsterDebugger 16
Installing AIR on an Android Device via a Server 16
Other Tools 16
Conclusion 18
3. Android . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
Android Software Development Kit 20
Installing the Android SDK 20
Installing the Android Debug Bridge 21
Detecting Your Device 22
Using the Dalvik Debug Monitor 22
Using the logcat Command 23
Using the Virtual Device Manager and Emulator 24
How Does AIR Run on Android? 25
Starting AIR with intent 25
AIR Access to Android APIs 26
Using the Command-Line Tool 27
A Basic Review 27
Conclusion 28
4. Permissions, Certificates, and Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29
Why Mobile? 29
The APK File 30
Creating the Application Icon 30
Choosing the Application Settings 31
Setting Permissions 33
Packaging External Resources 36
Signing Your Application with a Certificate 36
Versioning 37
Registering As an Android Developer 38
Publishing an Application on the Android Market 38
Uploading Assets 38
Listing Details 38
Publishing Options 39
Distributing Applications via Adobe InMarket 39
Publishing for the Amazon Market 40
Controlling Distribution by Using the MAC Address 40
viii | Table of Contents
16. Launching an AIR Application 41
Monetizing Your Application 41
Paid Applications 41
Mobile Ads 41
Reporting 42
Conclusion 43
5. Evaluating Device Capabilities and Handling Multiple Devices . . . . . . . . . . . . . . . . . 45
Hardware 45
The Processor 46
Memory and Storage 46
The Camera 46
Sensors 46
The Battery 46
The Display 47
Software 47
Performance 48
Capabilities 48
Orientation 49
Creating Content for Multiple Screens 50
Asset Scaling and Positioning 51
Vector Graphics or Bitmaps? 54
Developing a Deployment Strategy 54
Considering Connectivity 55
Conclusion 55
6. Opening and Closing an Application and Saving Data . . . . . . . . . . . . . . . . . . . . . . . . 57
The AIR Application 58
Opening the Application 58
Closing the Application 58
Moving Between the Background and Foreground 59
Setting Back, Menu, and Search Buttons 61
Overriding a Dimmed Screen 61
Why and How to Save Data 62
Internal or External Storage? 63
Local SharedObject 65
The Filesystem 66
Using the SQLite Database 70
Embedding a Database 76
Using Encrypted Local Storage 77
Conclusion 77
Table of Contents | ix
17. 7. Multitouch Technology . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 79
A Brief History 79
What Is Multitouch and Gesture? 80
How Does It Work? 80
The Multitouch Class 81
The GestureEvent Class 82
The Zoom Gesture 82
The Rotate Gesture 83
The Pan Gesture 85
The Swipe Gesture 86
The Press and Tap Gesture 87
The Two-Finger Tap Gesture 88
The TouchEvent Class 88
The GestureWorks Library 91
Designing for Touch 91
Conclusion 92
8. Accelerometer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 93
What Is a Motion Sensor? 93
The Accelerometer Class 93
Visualizing the Values 95
A Simple Animation 95
Updates and Screen Rendering 96
Setting Boundaries 97
Rotating Toward the Center 98
Shake Me 99
Smoothing Out Values 100
Conclusion 102
9. Camera . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 103
The Gallery Application and the CameraRoll Class 103
Selecting an Image 104
Adding an Image 109
The Camera Application and the CameraUI Class 109
Uploading to a Remote Server 111
EXIF Data 111
Conclusion 114
10. Geolocation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 115
Geolocation Classes 115
The GeolocationEvent Class 117
Locating a Device Using Global Positioning System and Network/WiFi
Technology 118
x | Table of Contents
18. Using GPS 119
Using the Cellular Network and WiFi 119
How to Know if GPS or WiFi Is Active 120
AIR and Android 121
Reverse Geocoding 122
Maps 124
Launching Google Maps 124
Static Maps 125
Dynamic Maps 129
EXIF Data and the Map Object 132
The speed Property 134
Conclusion 134
11. Microphone and Audio . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 137
The Microphone 137
Recording Audio 138
Playing Back Audio 139
Saving a Recording 140
Audio Assets 144
Embedding Files 144
Using External Files 144
Settings and the Audio Codec 145
Working with Sounds 147
Loading Sounds 147
Playing Sounds 149
Displaying Progress 149
Stopping Sounds 150
Resuming Sounds 151
Accessing Metadata 151
Audio Example Using Multitouch 152
ID3 Tags 152
Modifying Sound 152
Controlling Volume 152
Panning 154
Raw Data and the Sound Spectrum 154
Audio and Application Activity 158
Conclusion 158
12. Video . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 161
Preparing Video 161
Codecs 161
Bit Rate 163
Frame Rate 163
Table of Contents | xi
19. Resolution 163
Performance 164
Playing Video 164
Embedded Video 165
External Video 165
Progressive Video 165
RTMP Streaming 169
HTTP Dynamic Streaming 171
Peer-to-Peer Communication 171
Controls 171
YouTube 172
Capturing Video 172
Video and the CameraUI Class 172
The Camera Class 175
Documentation and Tutorials 176
Conclusion 176
13. StageWebView . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 177
The Native Browser 177
The StageWebView Class 178
Design Considerations 180
Local Use 181
Mobile Ads 182
Services and Authentication 184
Limitations 185
Conclusion 185
14. Hardware Acceleration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 187
Some Definitions 187
Rendering, or How Things Are Drawn to the Screen 188
Computation 189
Edge and Color Creation 189
Rasterization 189
Presentation 190
GPU Rendering on Android 190
The cacheAsBitmap Property 190
The cacheAsBitmapMatrix Property 193
The Display List 195
Memory Consumption 195
Tree Structure 196
Node Relationship 196
MovieClip with Multiple Frames 198
Interactivity 198
xii | Table of Contents
20. Multiple Rendering Techniques 199
Maximum Texture Memory and Texture Size 199
2.5D Objects 199
How to Test the Efficiency of GPU Rendering 200
Matrices 200
Identity Matrix 200
Transformation Matrix 201
Matrices for Multiscreen Deployment 202
Matrices Not to Be Used in GPU Mode 202
Hardware-Accelerated Audio and Video 203
Conclusion 203
15. Your Device and Others . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 205
RTMFP UDP 205
P2P Over a Local Network 206
Color Exchange 208
Companion AIR Application 210
P2P Over a Remote Network 210
Simple Text Chat 212
Multicast Streaming 213
End-to-End Stream 215
Directed Routing 217
Relay 218
Treasure Hunt 219
Other Multiuser Services 219
Arduino and Physical Computing 220
Conclusion 220
16. ViewManager . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 221
Navigation 221
ViewManager 221
Individual Views 225
Breadcrumb Navigation 232
Flash Builder ViewNavigator 234
Conclusion 237
17. Case Study . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 239
The Album Application 239
Design 240
Architecture 240
Flow 240
Permissions 243
Navigation 244
Table of Contents | xiii
22. THE BERNACLE GOOSE
Bernicla leucopsis (Bechstein)
Nesting abundantly in Greenland and in some numbers on
Spitzbergen, the Bernacle Goose is by no means uncommon in winter
along the west coast of the United Kingdom as far south as
Lancaster, as well as on the north coast of Ireland. Elsewhere in
these islands it is decidedly rare. It feeds on grass pastures near the
sea, almost invariably by night.
This species is commonly kept in captivity, where it breeds freely.
The crown of the head, neck, and upper breast are black; mantle
grey, barred with black and white; forehead, cheeks, and chin white.
Under parts greyish. Tail coverts pure white. Length 27 in.; wing 16
in.
23. 236
THE BRENT GOOSE
Bernicla brenta (Pallas)
This species is one of the most abundant of our Geese, and is found
in enormous flocks round our coasts throughout the whole
winter. It breeds along the west coast of Greenland and also
on the islands and northern coasts of Russia and Siberia. It feeds
chiefly by day, and is fond of wading about in mud-flats or in shallow
water feeding on aquatic vegetation.
The whole plumage is chiefly black, except the tail coverts, which are
white, and a white patch on each side of the neck. Length 22 in.;
wing 13 in.
24. 237
THE WHOOPER SWAN
Cygnus musicus, Bechstein
Formerly breeding in small numbers in the Orkneys, this species now
only visits us during the winter, its numbers depending largely on the
severity of the climate in Northern Europe. It frequents bays,
estuaries, and inland lakes, feeding on weeds and aquatic vegetation.
The note is a loud “whoop, whoop, whoop,” from which its trivial
name has been derived, and is often uttered as they fly along the
shore in a long straggling line. The sexes are alike in plumage, as are
all palæarctic Swans, and this species may be distinguished by the
colour of the bill, which is black at the tip and yellow at the base, the
yellow extending forward beyond the openings of the black nostrils.
The base of the bill is flat and quadrangular and not knobbed as in
the Mute Swan. Length 60 in.; wing 25·5 in.
25. BEWICK’S SWAN
Cygnus bewicki, Yarrell
This species, which is smaller than the Whooper, visits us regularly
every winter, and is in some places the commoner of the wild Swans.
In Scotland it is abundant in some seasons as it is also in Ireland, but
on the coasts of England and Wales it is always rather scarce. It
breeds in the Far North to the east of the White Sea.
It may be distinguished from the Whooper by its smaller size and the
extent of the yellow on the beak, which does not quite reach the
nostrils. Length about 46 in.; wing about 21 in.
26. 238
THE MUTE SWAN
Cygnus olor (J. F. Gmelin)
In this country the Mute Swan is only met with in a state of semi-
domestication, having been introduced at some early period of
history. It is now, however, widely distributed throughout our islands.
Inhabiting lakes, rivers, and ornamental waters, it feeds on aquatic
weeds and grain, and is extremely useful in preventing an undue
growth of weeds in ornamental ponds and lakes. The nest is a huge
structure of straw and rushes, built upon the edge of the water, or in
the centre of a reed-bed. The eggs, which vary in number
from five to nine or ten, are of a uniform pale green, and are
hatched after some five weeks’ incubation.
The young, which are covered at first with greyish down, are
carefully tended by both parents, and when tired nestle on their
parents’ back. In olden times the right to keep Swans on the Thames
was granted by the King to many of the City Companies, and in the
autumn of each year (a custom which is still continued) the young
Swans are caught up and marked on the bill with the private mark of
the Company to whom they belong. This is known as “Swan upping.”
The male is known as the “Cob” and the female as the “Pen,” and the
rules and regulations clearly state how the brood shall be awarded in
the event of the Cob and Pen belonging to different Companies, while
the landowner on whose ground they nest also comes in for a share.
At the nest the male Swan is very savage, attacking any intruder with
his bill and with savage beats of his powerful wings; his mate,
however, is very quiet and will allow herself to be pushed off the nest
with no stronger protestation than a subdued “hiss.”
27. 239
This Swan is not mute as its name implies, but has a loud trumpet-
like note, to which, however, it seldom gives utterance.
In a purely wild state, this species may be found breeding in
Denmark and the south of Sweden, and it is a common breeding
species in South-eastern Europe. From its northern breeding haunts it
migrates in winter, many probably coming over to our shores.
The plumage is pure white; the bill reddish orange with a
black knob at its base. This knob is much larger than in the
male. The young are greyish drab. The so-called “Polish Swan” is a
variety of this species, in which the young are white. Length about 56
in.; wing 27 in.
28. 240
THE COMMON SHELD-DUCK
Tadorna cornata (S. G. Gmelin)
Although somewhat local in its breeding haunts, this species is fairly
abundant round all our coasts in winter. It is a Sea-Duck, being
seldom found far inland, and its food consists of small mollusca and
marine insects, which it seeks on our flat estuaries and along the
shore.
A rabbit-burrow in sand-dunes near the sea is chosen for a nesting-
site, and lined with a little grass, to which is subsequently added an
abundance of grey down from the body of the female. Occasionally it
makes its own burrow, or other sites such as crevices between
boulders or under furze bushes are selected. The eggs, generally ten
in number, are creamy white. As soon as they are hatched the
mother leads her brood to the shore, where they feed, making for the
sea on the first sign of danger.
During the pairing season this bird is very noisy, the male uttering a
short whistle, while both sexes run round each other with out-
stretched neck, making a curious guttural chuckle.
In winter large flocks of these birds visit us from the Continent.
These flocks may be seen resting out at sea by day and come
in to feed on the soft ooze by night; they are of course more
partial to flat and sandy parts of the coast, but may nevertheless
often be found in small sandy bays on an otherwise rocky shore.
The head and neck are glossy bluish black; the scapulars and
primaries black. There is a broad band of bright chestnut across the
back and breast, and a black stripe along the centre of the under
29. parts. Speculum green. The rest of the plumage is pure white. Legs
flesh pink; bill crimson. The sexes are alike, but the female is smaller
and duller. The male has a crimson knob at the base of his bill which
swells up considerably during the breeding season.
The young bird lacks the chestnut band, the head and neck are dull
brownish black, the scapulars greyish brown, and in its first autumn it
assumes a plumage similar to the adult female, but duller. Length 25
in.; wing 13 in. Both sexes assume in July a much duller plumage,
somewhat resembling that of the young in their first winter.
30. THE RUDDY SHELD-DUCK
Tadorna casarca (Linnæus)
The Ruddy Sheld-Duck is a South-eastern European species, breeding
on the shores of the Levant and throughout Northern Africa, but it is
rare on the north shores of the Mediterranean west of the Adriatic. It
has several times been noted as a straggler to England, and in 1892
many flocks appeared in different parts of the country.
31. 241
SHELD-DUCK
Tadorna cornuta
The general colour is a deep orange brown, the head being
rather lighter. The male has a narrow black collar during the
nesting season. The female is much paler on the head, the forehead,
lores, and a ring round the eye being nearly white. Length 25 in.;
wing 14·5 in.
32. 242
THE MALLARD OR WILD DUCK
Anas boschas, Linnæus
This is at once our commonest and most beautiful Duck. Owing to
drainage of fen-lands and higher cultivation it is, perhaps, not so
abundant as formerly, yet there are few marshes or low-lying lands of
any extent in our islands, which do not afford a home to a few pairs
of this species.
It feeds chiefly by night on worms, aquatic insects, water weeds, and
grain, and prefers ditches overgrown with weeds or shallow ponds to
open stretches of deep water. Early in March it chooses a nesting site,
usually on the ground and at no great distance from water, but
exceptionally it has been known to nest in trees, faggots, stacks, and
other elevated places. No nest is formed, but a cup-shaped hollow is
scraped out, which is warmly lined with down after incubation
commences. The eggs, usually ten to twelve in number, are pale
greenish yellow, and are always carefully covered up by the Duck on
leaving the nest. They hatch after twenty-seven days’ incubation, and
the young are then taken to the nearest water, on or near which they
remain for about two months till they can fly. If, however, they
are much disturbed they will be led away by their mother to a
neighbouring piece of water, often at some considerable distance.
In a wild state the Mallard, as the male of this species is called, is
strictly monogamous, and during the whole of incubation he will
remain in the vicinity of the nest, warning his mate of the approach
of danger, and accompanying her when she comes off to feed. Once
the young are hatched he retires to some secluded and sheltered
piece of water, where he assumes a dull plumage, somewhat
resembling that of the female. During this period he becomes very
33. skulking, rarely showing himself on the open water. When his dull or
“eclipse” plumage has been assumed, he casts all his flight feathers
at once, and for a short time becomes incapable of flight. These grow
again in about a fortnight, and then in September he begins to
assume his brilliant colours once more, and comes from his secluded
retreat to join his comrades. In the winter they gather in large flocks,
which resort to open sheets of water or the sea, flighting every
evening to the marshes and shore to feed, and retiring again at
daybreak to rest on the water.
MALLARD OR WILD DUCK
Anas boschas
34. 243
244
It is these daily movements of Duck that are known to
sportsmen as “flights,” and they afford excellent shooting to
the gunner concealed on their route. Vast numbers of this and other
species of Duck used formerly to be taken in decoys, but partly owing
to decrease in the numbers of the fowl, or still more to the increase
of shooters, who frighten them away, few if any decoys are now
worked at a profit in this country. A decoy is a pond in a suitable
locality near the sea surrounded by trees and having two or four
curved arms known as “pipes” running up at the different corners.
These pipes are covered with netting, and end in a small bag net.
The Duck are enticed up by tame birds and by means of a red dog
that they follow out of curiosity. When some way up the pipe they
see behind them the decoyman, who has hitherto been concealed by
an ingenious arrangement of reed-screens, and rather than turn back
and face him, they rise and fly up the pipe into the net. The whole
operation must be carried out in silence so as not to scare the other
birds on the pond, who remain in complete ignorance of their
comrades’ fate. Absolute quiet and plenty of food are the essentials
for the successful working of a decoy. They are still used in Holland,
where they form a considerable source of profit to their owners; their
number is limited, and a licence has to be paid for each decoy.
After the brood can fly the Duck loses her primaries and becomes
incapable of flight for a short time, but as soon as her quills are
grown the whole family move off to join the flocks, which are now
rapidly forming. Large numbers visit us yearly from abroad, and a
spell of severe weather in midwinter still further increases their
numbers.
The male has a glossy green head and neck, the latter being
encircled by a narrow white ring; rump and tail coverts glossy
greenish black, the four central coverts upturned; chest and breast
deep chestnut; rest of under parts pale grey, vermiculated with black;
bill greenish yellow; legs orange. The Duck is dark brown, the
feathers having paler edgings. The young resemble the female, but
the males have assumed their full dress by October. The male
35. in eclipse has a plumage which approximates to that of the female.
Length 23 in.; wing 11 in.
36. 245
THE GADWALL
Anas strepera, Linnæus
The Gadwall is a scarce visitor to our shores, occurring irregularly
along the east coasts of Scotland and England, but it is very rarely
seen in the west or in Ireland. In a few places in Norfolk, where it
was originally introduced, it breeds, and has of late years
considerably increased both there and in the surrounding counties. In
habits it resembles the Mallard. The eggs are usually ten in number
and of a delicate creamy pink. It may be easily recognised on the
wing by its white speculum.
On the Continent it nests in Central and Eastern Europe, its breeding
range extending to the far north of Russia. It winters in the
Mediterranean basin.
The adult male is greyish brown, with darker mottlings on the head
and neck; back dark brown, with greyish markings; median wing
coverts chestnut; greater coverts almost black. Under parts white,
grey on the flanks and vent. Under tail coverts black. The female is
marked with dark brown and buff much like a Wild Duck, but is
recognisable by the white speculum. The young somewhat resemble
the female. The white speculum forms a distinctive mark of this
species at all ages. Length 20 in.; wing 10·5 in.
37. 246
THE SHOVELLER
Spatula clypeata (Linnæus)
This bird is by no means rare with us in winter, when large numbers
come over from abroad. It is essentially an inland species, preferring
small and sheltered pieces of water rather than wide open stretches.
Its most characteristic feature is the large flattened bill with which it
feeds on the surface-swimming animalculæ and other insects, the
broad lamellæ of the mandibles forming an efficient strainer. When
feeding three or four will often follow each other in a circle, each
feeding in the other’s wake. Of late years it has become more
numerous as a breeding bird, and it now nests commonly in the
Broads and other districts of Norfolk and the eastern counties. In
Kent and the Midlands, Yorkshire and the North, it nests sparingly, as
well as in some of the southern and eastern counties of Scotland. In
Ireland it is a local but by no means scarce species. Except in the
breeding season it is a very silent bird; when courting it moves its
head up and down, uttering a low “took, took,” which is answered by
the female. The nest is generally placed at some distance from the
water in the middle of a dry grass-field, where there is hardly any
cover beyond a small patch of grass more luxuriant than the rest.
The eggs, which number from eight to ten, are pale greenish buff in
colour. The female sits very closely, and the male remains in
attendance at no great distance and accompanies her when
she comes off to feed. The incubation period of this species is
rather shorter than with most Ducks, and lasts between twenty-one
and twenty-three days. The young are solely looked after by the
Duck, and when first hatched their bills show no trace of the
broadening and flattening, characteristic of the adult.
38. During the summer the Drake assumes an “eclipse” plumage, which
somewhat resembles that of the Duck. In October he begins, unlike
most other species, to assume an “intermediate” plumage, in which
the head is very dark but not metallic, and the white of the breast is
obscured by dark transverse bars. The full plumage is not usually
complete till the end of February or early in March.
In this country our breeding birds are practically resident, only
shifting from their nesting-quarters when frozen out. The majority of
birds met with, however, in winter are immigrants from the
Continent, who leave us again in March.
The adult Drake in full plumage is a beautiful bird. The head and
upper neck are metallic green; lower neck, breast, and scapulars
white; back brown; shoulders pale blue; greater wing coverts white.
The under parts are deep chestnut; speculum green; bill black; legs
orange.
The Duck is dark brown, with light rufous buff edgings to the
feathers. Shoulders bluish. The young at first resemble the Duck, and
in November begin to assume the “intermediate” plumage described
above, except that the breast feathers are spotted and not barred. It
does not always assume its full plumage in the first year.
40. 248
THE PINTAIL
Dafila acuta (Linnæus)
This species visits us in large numbers during the winter, arriving in
September and not leaving our shores till April. During this period it is
essentially a Sea-Duck, haunting shallow shores and estuaries, where
it feeds on aquatic vegetation, crustacea, and other animal life
brought in by each tide. It is commoner on the east coast than
elsewhere owing to the large tracts of shore suited to its habits, but it
may be found in smaller numbers on the west and in Ireland,
wherever suitable localities exist.
It is only of late years that it has been known to nest in this country,
a small colony having established themselves on one of the Scotch
lochs. Elsewhere it breeds abundantly throughout Northern Europe,
migrating southwards in winter. The nest is placed in a dry situation,
at some little distance from the water. The eggs are rather elongated
in shape and pale buffish green in colour.
The adult male has a brown head, greenish black on the nape. A
white stripe runs down the neck on either side, merging into the
white of the under parts. Back and flanks dark brown, mottled with
grey. Wing coverts buff; speculum bronze green; tail black, the two
central feathers much elongated; under tail coverts black; bill and
legs slate grey. The female is of varying shades of buff and brown.
The elongated neck and general shape of this species is sufficient to
distinguish it from others of its family. The young resemble
the female, and moult directly into their full plumage in their
first autumn. The eclipse plumage of the Drake, which is dark brown
above and smoky grey below, is lost about October. Length 26 in.;
wing 11 in.
41. 249
THE TEAL
Nettion crecca (Linnæus)
This is the smallest of our native species of Duck, and is fairly
common throughout our islands at all times of the year, but its
numbers are largely augmented in winter by the arrival of vast flocks
from abroad. It may be found in winter near the mouths of rivers and
shallow estuaries as well as inland; its food consists of grain, insects,
worms, slugs, and molluscs.
It breeds throughout our islands, but more abundantly in the north.
The nest is generally placed at some distance from water on a dry
moorland or rough grass-field, and this species makes a rough nest
of leaves and grass, lined with down. The eggs, eight to ten in
number, are creamy white.
The male has the crown, nape, cheeks, and throat chestnut; an
elongated patch of purplish green behind the eye, the rest of the
upper parts vermiculated with black and white except the rump and
tail coverts, which are black. Under parts white, the lower part of the
neck and breast being spotted and sometimes of a yellowish tinge;
flanks vermiculated with black. Speculum green and purplish black.
Bill black, legs brownish grey. The female is mottled with
brown and buff. The young resemble the female. The male in
his eclipse dress, which is worn till late in October or November,
resembles the female very closely, more so in fact than is the case
with any other species. Length 14·5; wing 7·25 in.
42. THE AMERICAN GREEN-WINGED
TEAL
Nettion carolinense (J. F. Gmelin)
This species has only occurred three or four times in these islands.
The male differs from the Common Teal in having some greyish
vermiculated feathers on either side of the breast, and the buffish
white lines on the face are very slightly defined. The female cannot
be distinguished from our native species. Length 16 in.; wing 7·25 in.
43. 250
THE BLUE-WINGED TEAL
Querquedula discors (Linnæus)
This American species has been taken at least once in the United
Kingdom. The male has the throat, forehead, and crown dark lead
colour, and a long crescentic patch of white in front of the eye.
Cheeks and neck dull lavender grey. Length 16 in.; wing 7·25 in.
44. 251
THE GARGANEY
Querquedula circia (Linnæus)
This is one of our scarcest species, coming to us as a summer
immigrant from April to September, and remaining in a few suitable
spots to breed. It is commonest in Norfolk, and may also be found in
Hants, Kent, Suffolk, and Yorkshire. Elsewhere its occurrences are
rare and only consist of stragglers on migration.
It breeds regularly on the Continent from Sweden southwards,
becoming commoner in the east.
The nest is usually placed in a dry and often open situation, where
there is but little cover. The eggs resemble those of the Teal, but are
rather greener in tint.
The crown and nape of the male are dark brown, with a conspicuous
white stripe passing backwards over the eye. Cheeks and neck brown
ticked with white. Back dark brown; wing coverts bluish grey. Chin
black; breast pale brown, with dark crescentic bars; remainder of
under parts white. Vermiculated on the flanks. Speculum green; bill
black; legs greenish. Female somewhat similar to Duck of the
common Teal, but may be distinguished by the presence of a light
stripe over the eye. The feathers of the back are dark with light
margins, not barred as in the Teal, while the feathers of the breast
are also entirely dark with white margins. Length 16 in.; wing 7·8 in.
45. 252
THE WIGEON
Mareca penelope (Linnæus)
The Wigeon is one of our commonest winter visitors, arriving in large
numbers from early in September onwards, and frequenting
estuaries, bays, and tidal waters, but rarely wandering far inland.
Although feeding also on marine insects and crustacea, it is chiefly a
vegetable eater, living almost entirely upon Zostera marina.
In Scotland a good many pairs remain to breed, and during the
summer it frequents high moorlands and inland waters. The nest is
placed in a tuft of rushes or among heather, and the eggs, usually
ten in number, are of a delicate creamy white. The note is a
melodious whistle, which may be expressed as “whee you.”
The male has the head and neck chestnut, with a broad buff stripe
extending backwards over the crown; back grey uniformly
vermiculated; throat and upper neck chestnut; breast white,
vermiculated on the flanks; shoulders white; speculum green. In the
eclipse plumage the head is dark chestnut, grizzled with brown; back
brown, with chestnut edgings to the feathers; flanks chestnut; under
parts white. The female is dark brownish grey above, lighter on the
wing coverts, and white underneath. Length 18·5 in.; wing 10·5 in.
46. THE AMERICAN WIGEON
Mareca americana (J. F. Gmelin)
One or two examples of this species have occurred in this country at
long intervals. It may be distinguished from our Wigeon by the
forehead and crown being dull white, the cheeks and neck whitish,
speckled with brown, and a green stripe passing backwards from the
eye. The female has the head and neck yellowish white, speckled
with black. Length 19 in.; wing 10·25 in.
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