Journal of Threatened Taxa |
www.threatenedtaxa.org | 26 July 2021 | 13(8): 19029–19039
ISSN 0974-7907 (Online) | ISSN 0974-7893
(Print)
https://doi.org/10.11609/jott.6362.13.8.19029-19039
#6362 | Received 05 July 2020 | Final
received 15 June 2021 | Finally accepted 17 June 2021
Identification of a unique barb
from the dorsal body contour feathers of the Indian Pitta Pitta
brachyura (Aves: Passeriformes: Pittidae)
Prateek Dey
1, Swapna Devi Ray 2, Sanjeev Kumar Sharma 3,
Padmanabhan Pramod 4 &
Ram Pratap Singh 5
1–5 National Avian Forensic
Laboratory, Sàlim Ali Centre for Ornithology and
Natural History, Anaikatty, Coimbatore, Tamil Nadu
641108, India.
5 Department of Life Science,
School of Earth, Biological and Environmental Sciences, Central University of
South Bihar, Gaya, Bihar 824236, India.
1 pratikdey23@gmail.com, 2 swapnadray555@gmail.com,
3 sksbreeder@gmail.com, 4 neosacon@gmail.com, 5 rampratapsingh81@gmail.com
(corresponding author)
The Communication published in the 26 June
2021 issue of JoTT was withdrawn due to a faulty map.
The same Communication with a corrected map is published here.
Editor: P.O. Nameer,
Kerala Agricultural University, Thrissur, India. Date
of publication: 26 July 2021 (online & print)
Citation: Dey,
P., S.D., Ray, S.K. Sharma, P. Pramod & R.P. Singh (2021). Identification of a unique barb
from the dorsal body contour feathers of the Indian Pitta Pitta
brachyura (Aves: Passeriformes: Pittidae). Journal of Threatened Taxa 13(8): 19029–19039. https://doi.org/10.11609/jott.6362.13.8.19029-19039
Copyright: © Dey
et al. 2021. Creative Commons Attribution
4.0 International License. JoTT allows unrestricted use, reproduction, and
distribution of this article in any medium by providing adequate credit to the
author(s) and the source of publication.
Funding: This work was funded and supported
by Ministry of Environment Forest and Climate
Change (MoEFCC), Government
of India.
Competing interests: The authors
declare no competing interests.
Ethics statement: This research was conducted in
compliance with the government guidelines.
Author details: Prateek Dey is a doctoral candidate of zoology (avian genetics) at SACON, has a
degree in Integrated M.Sc (Life Sciences) from
Central University of Tamil Nadu. Currently he works on whole genome sequencing
and develops feather markers, for bird species prevalent in illegal wildlife
trade. Swapna Devi Ray is a
researcher from ecology and environmental Science background. Previously worked
as a Junior Research Biologist at National Avian Forensic Laboratory, SACON.
Currently affiliated as a Ph.D. scholar at SACON working on wildlife crime, plumology and molecular markers of avian species. Dr. Sanjeev Kumar Sharma has a PhD in
Animal Genetics and Breeding from National Dairy Research Institute worked as a
Project Scientist at the National Avian Forensic Laboratory, SACON. He carried
out significant work generating whole genome sequences and developing feather
markers for select bird species prevalent in illegal trade. Dr. Padmanabhan Pramod is a Senior
Principal Scientist and head of Nature Education programme
at SACON. Over a period of 27 years he has carried out various research
projects in the field of ecosystem assessments, eco-development and mitigation
measures for the bird hazards to aircrafts.
Dr. Ram Pratap Singh is
Associate Professor of Life Science at the Central University of South Bihar.
The primary focus of Dr. Singh’s research is to understand the physiology and
genetics of birds and other animals. He established National Avian
Forensic Laboratory and started Genome Resource Bank at SACON.
Author contributions: R.P.S collected the sample;
conceived the idea; and supervised the research. R.P.S and P.P generated the
funds for the study. P.D, S.D.R and S.K.S generated the data. R.P.S and P.D
wrote the manuscript and analyzed the data. All the authors reviewed the
manuscript.
Acknowledgements: We are also thankful to the Tamil
Nadu Forest Department for providing the permission to collect dead birds.
Abstract: Earlier research on feather
morphology emphasized comprehensively on the body contour feather than various
other types of feathers. Therefore, we conducted a systematic study on all
feather types of the Indian Pitta Pitta brachyura, a passerine bird native to the Indian
subcontinent. Feather barbs from wing contour, tail contour, body contour, semiplume, down, powder down, and bristle feathers were
retrieved from the bird and observed under a light microscope. Primary flight
feathers from the right and left wing were longest (85.17 mm and 87.32 mm,
respectively), whereas bristle feathers were the shortest (5.31 mm). The mean
barb length was observed to be the highest (11.37±0.47 mm) in the wing feather
followed by body contour (8.31±0.39 mm), semiplume
(8.27±0.22 mm), tail feather (7.85±0.50 mm), down (6.45±0.21 mm), powder down
(6.04±0.23 mm), and bristle (2.70±0.07 mm).
Pearson correlation was found positive for barb length and feather
length of down feathers (r= 0.996, p ≤0.05). We observed a novel type of barb
the first time from dorsal body contour feather having plumulaceous
barbules at the base followed by pennaceous barbules. This unique barbule
arrangement is termed ‘sub-plumulaceous’ as it is
distinct and analogous to known ‘sub-pennaceous’ type arrangement found absent
in passerines.
Keywords: Feather, microscopy, Pitta brachyura, sub-pennaceous.
INTRODUCTION
Feathers are
the most numerous, elaborate, and diverse derivatives of avian integument (Gill
1995). Collectively referred to as plumage, feathers are extraordinary
evolutionary innovation evolved over a million years that perform a wide
variety of functions in birds from insulation, protection, mate attraction,
sound production to locomotion (Gill 1995; Lovette
& Fitzpatrick 2016). All birds have different types of feather assorted in
their plumage (Gill 1995). These feathers vary considerably in macroscopic
(colouration, texture, pattern, shape, and size) and microscopic characteristics (minute
morphological appendages) (Dove 1997a). The studies on types, characterisation
and microstructures of feathers give us a deeper understanding of feather form
and function (Lee et al. 2016). Although a handful of studies on feather
examination have been reported over the years, still many questions regarding
feather morphology have not been answered (Lee et al. 2016). Morphological
examination of feather structures in the present day has acquired importance in
diverse range of disciplines such as phylogeny (Dove 1997a ; Bensch et al. 2009), palaeontology (Messinger
1965; Dove et al. 2010), archaeology (Harwood 2011), avian ecology (Galván 2011; Fairhurst et al. 2013), wildlife forensics
(Dove & Coddington 2015), biomechanics (Kulp et
al. 2018), and material sciences (Lingham-Soliar
2017).
Typically a
feather is made of a central rod like staff with numerous interlocking barbs
attached to it on either side. The central shaft of each barb has minute branch
like structures called barbules (distal/proximal) that extend on its either
side (Images 1, 2). Barbules can be either pennaceous /plumulaceous
and harbour various microstructures such as hooklets,
nodes, internode, cilia, villi, prongs etc. Though individual groups of
feathers may vary amongst themselves on various accounts of functionality, they
share vast similarities in certain basic structural characters (Gill 1995). The
literature regarding the nomenclature of feather structure and its micro
characteristics till date lacks uniformity and is mostly based on convenience
of the authors (Lovette & Fitzpatrick 2016). The
authors would also like to shed light on the fact that many intermediate and exceptions
might exist within the nomenclature used in this report. Adapting from various
previous text books (Chandler 1916; Gill 1995; Lovette
& Fitzpatrick 2016) and research papers we have resorted to widely
applicable terminology based on most logical nomenclature perceived by the
authors.
Over the
years very few research reports have been published on feather identification
and its structural characterisation (Lee et al. 2016). A few notable and
exceptional reports do exist in the discipline of feather studies. In this
particular aspect, a landmark work on feather characterisation and systematic
studies was done by Chandler (1916). In his work Chandler (1916) adopted a
universal nomenclature for various microstructures in a feather and classified
feathers into plumules (unspecialized plumules, powder down, oil gland
feathers, and nestling types), filoplumes, and
contour (remiges, retrices, unspecialized contour
feathers, ornamental plumes, ear coverts, facial bristles, and facial ruffs).
In 1965, Messinger with the help of Hargrave
successfully standardized a method to identify feather fragments from
archaeological feather remains (Hargrave 1965; Messinger
1965). Day in 1966 studied the microstructures of plumulaceous
barbs of contour feathers to identify various species of birds, using basic
methodology as described by Chandler (Day 1966). Robertson (1984) studied plumulaceous barbs of contour feathers and prepared a
detailed scheme for species identification from feather microstructure. He
quantified the numerical variations in feather microstructure amongst species
by measuring the length of barbules and number of nodes per barbules thus
addressing the lack of numerical evidences in Chandler’s (1916) work. In recent
times, Carla J. Dove (Dove 1997a, 2000) used plumulaceous
barbs of body contour feathers to successfully demonstrate inter-species
differences and develop various forensic techniques useful in identification of
species. In 2015, Lee and colleagues used the microstructures in plumulaceous barbs of body contour feathers for taxonomic
identification of Australian birds (Lee et al. 2016). The study was remarkable
in the fact that it used simple methods inspired from Chandler (1916) to create
a feather identification catalogue of various illegally traded birds in
Australia.
Previous
studies on feather morphology are inclined in the direction of species
identification and phylogenetic differentiation ( Robertson et al. 1984; Dove
1997a, 2000). Barring Chandler (1916), previous reports have cleverly avoided
elaborating on micro-structural differentiation in different ‘groups’ of
feathers, selecting mostly ‘body contour feathers’ from the breast region as
the subject of study. Such studies elaborated more on species differentiation
but created a considerable knowledge gap in the understanding of differential
structural characteristics of various types of feathers present in an
individual bird. Most of the previous studies on feather investigations have
been conducted either in bird species of northern America or Australia (Dove
& Coddington 2015; Lee et al. 2016). Very few minor reports have been
published on birds of southern Asia (Songyan et al.
1995; Lee et al. 2010) and even fewer reports about feather morphology of bird
species of Indian subcontinent has ever been published. With absolutely no
in-depth reports of feather morphological studies of birds of southern Asia
(birds of Indian subcontinent in particular) has led to a considerable
knowledge gap in this particular aspect. Therefore, our group has taken an
initiative to create a feather atlas for Indian birds, and this study is a part
of the same feather atlas initiative.
The main
objective of this study is to quantify macro and micro characteristics of
various types of feathers from different anatomical locations of an individual
bird species, the Indian Pitta Pitta brachyura. Secondly, we aim to create the very first
comprehensive report on feather morphological examinations in any endemic
species of bird of the Indian subcontinent. Third, we aim to standardize a
protocol that can be used for systematic identification and morphological
studies of various applied aspects of feather investigations. The implications
of our study can inculcate a whole range of in-depth feather analysis as a tool
for feather form and function elaboration or as a phylogenetic identification
tool or can be used for applied wildlife forensic research.
METHODS
Target bird description
The Indian
Pitta is a member of the Pittidae family of the order
Passeriformes. Classified under IUCN category as ‘Least concern’, one such
individual was found dead in the premises (11.0590N, 76.8140E)
of our institute and was used as a specimen for this study. The dead specimen
was collected with due permission from forest department (Ref.No.WL5
(A)/2219/2018; Permit No. 14/2018). Covering a large range, the Indian Pitta
migrates to various parts of peninsular India during winter (Figure 1). Generally the Indian Pitta is
extant up to an elevation of 1,700 m in the entire peninsular India inhabiting
deciduous and evergreen forests (Lambert & Woodcock 1996).
Feather sampling
We classified
feathers broadly into contour (wings, tail, and body contour) and non contour (semiplume, down,
powder down, bristle, and filoplumes) category (Gill
1995). Wing feathers were further sub-divided into primary flight feathers and
secondary flight feathers following Lovette &
Fitzpatrick (2016). The specimen was searched meticulously to collect all the
various types of feathers. One primary flight feather, one secondary flight
feather each from left and right wing was sampled along with a single feather
from the tail. Similarly, one body contour from the ventral side and another
body contour from the dorsal side of the bird were sampled. In case of semiplume, two feathers each from ventral and dorsal side
of the bird and one feather from the tail were sampled. One feather each from
ventral portion, dorsal portion, right wing, left wing and tail were sampled
for down feathers. In the same way, one feather each from ventral portion,
dorsal portion, right wing, left wing, and tail were sampled for powder down
feathers. Five bristle feathers were sampled from the chin and orbital region
of the bird. After repeated searches through the cadaver of Indian Pitta, filoplume feathers couldn’t be identified leading to
omission of Filoplume observations in this study. The
feathers were plucked carefully using surgical forceps (number 00) during
sampling (Image 3).
Feather barb sampling
A methodical
representation of the number of barbs sampled are mentioned in Table 1. After a
feather was carefully plucked from the specimen, it was cleaned using 70 %
ethanol solution (Lee et al. 2016). At first, each feather was placed carefully
on a plain paper along with a scale, labelled properly and photographed. The
length of the feather was noted and the feather was marked into three equal
intervals termed ‘proximal’, ‘intermediate’, and ‘distal’ sections,
respectively (Dove 1997b) (Image 4). For wings and tail feathers, vanes were
classified as outer vane and inner vane following Chandler (1916) (Image 4).
Three barbs from both vanes (inner and outer) of each section (proximal,
intermediate, and distal) from a single feather from wings and tail were
sampled (Image 4). A total of 18 barbs were sampled from each of the wing and
tail feathers (5 feathers in total) (Table 1). For other types of feathers
(body contour, semiplume, down, and powder down) five
barbs from each of the three sections (proximal, intermediate, and distal) were
plucked carefully following the same sampling procedure. Due to the minute size
of the bristle feathers five entire bristle feathers were mounted onto separate
glass slides. All the samplings of barbs were conducted carefully using
surgical forceps (number 00) with minimal damage to the barbs.
Feather barb slide preparation
The sampled
feather barbs/whole bristle feathers were placed onto a small drop of Xylene
(Fisher Scientific, product No. 35405) on a microscope glass slide which were
previously cleaned by using 70% ethanol. The drop of Xylene allowed the feather
barbs to spread apart its barbules and after its evaporation kept the barbs
attached onto the glass slide (Lee et al. 2016). In the meantime the slides were labelled
properly using printed label stickers according to their slide codes to avoid
confusion. Previously cleaned cover glasses were placed directly onto the
completely dried feather barbs for dry mount (Lee et al. 2016). By using nail
varnish (Nail Trend; Pearl White, India) the four sides of the cover glasses
were sealed and allowed to dry for proper microscopic observations.
Macroscopic characteristics
Whole
feathers were observed for macro-characteristics such as feather colour, pattern and texture following Lee et al. (2016). As
mentioned above, the feathers were placed on a plain paper along with a scale,
labelled properly and photographed. The slides mounted with barbs were also
placed carefully on a plain paper along with a scale and photographed. Using
ImageJ software distance (in the digital images) was standardized using the
scale in each individual photograph (Schneider et al. 2012). Using the same
ImageJ software length of feathers and length of each barb was calculated
following the software as per instructions. Length of all the feather types was
calculated, except powder down feathers because these feathers have extremely
soft and rudimentary rachis,leading to no distinct
orientation.
Microscopic characteristics
All the
prepared slides were observed carefully for a number of selected microscopic
features of feather barbules. These parameters include presence or absence of
sub-pennaceous region, villi, nodes, prongs, hooklets
and ventral teeth; shape of nodes and internodes; presence of prongs, hooklets and ventral teeth on both side of barb; size of
prongs and pigmentation of nodes, internodes and ramus (Image 5).
The slides
were observed at 100X or 400 X magnifications under a light microscope (Weswox BXL, India) for select microstructures.
All the
feather observation and recording were carried out by a single observer to
minimize observer bias. Important microscopic morphological characters were
photographed using binocular light microscope with an attached camera (Labomed Lx500, India) at 100X and 400X magnifications using
Image aR software.
Statistical analysis
All the
analyses were performed using MS-Excel (Microsoft, U.S.A) (with XLSTAT add-in
software). We calculated the length of all the sampled feathers as well as the
length of barbs sampled from these feathers. For descriptive analysis the
feathers were grouped into six groups (wings, tail, body contour, semiplume, down, powder down, and bristle) (Table 2). For
each group the mean barb lengths, standard error, range and coefficient of
variation was calculated. Comparative analysis were made and presented as box
and whiskered plots (Figure 2). Correlation between the mean barb length and
feather length was calculated using Pearson correlation coefficient. The
feathers were grouped into four groups (contour, semiplume,
down, and bristle), powder down was excluded from this analysis as the length
of powder down feathers couldn’t be calculated. For each feather, length of the
feather was paired with mean barb length (of all the sampled barbs) during
correlation analysis.
RESULTS
We observed
370 feather barbs from 27 different feathers (Table 1). We found morphological
features such as hooklets and ventral teeth that were
exclusive to contour and semiplume feathers only
(Table 5). Features such as villi, nodes, prongs and internodes were recorded
in down, powder down, semiplume feathers as well as
in body contour feathers also (Table 5).
We observed a
unique uncharacterized barbule arrangement in body contour feather barbs (Image
13). The barb was composed of plumulaceous barbules
at the base of the barb with pennaceous barbules immediately following it (Image
13). Such unique arrangement of barbules in barbs was named as “sub-plumulaceous region” and was observed exclusively in the
intermediate section of body contour feathers from the dorsal portion of the
bird (Image 13). We reported in this study for the first time that bristles
display microscopic morphological characteristics similar to down or powder
down feathers (Image 12) (Table 5). The barbs of bristle feathers were
characterized by the presence of villi, nodes, prongs and absence of hooklets and ventral teeth same as in down and powder down
feather types. Even the shape of nodes was exactly similar as recorded in down
and powder down feather barbs (Image 12).
Macroscopic characteristics
Primary
flight feathers from the right and left wing (Table 1) were measured longest
(85.17 mm and 87.32 mm, respectively), whereas bristle feather was the shortest
(5.31 mm) (Table 1). The mean barb length of the wing feathers (primary and
secondary flight feathers of left and right wing of contour type) was observed
to be the highest (11.37±0.47 mm) and shortest in bristle (2.70±0.07 mm) (Table
2). Correlation (Pearson correlation coefficient) calculated using pair-wise
comparison indicated that correlation was positively high for only the pair of
barb length and feather length of down feathers (r= 0.996, p ≤0.05) other
feather types (contour, semiplume, powder down, and
bristle) had no significant correlation between barb length and feather length
(Table 3). The findings for various attributes (colour
of feather, pattern in vanes, texture of barbs, and texture of rachis) of
different feathers groups are presented in Table 4.
Microscopic characteristics
The feathers
were divided into groups (wings, tail, body contour, semiplume,
down, powder down, and bristle) and microscopic structures were scored in a
predominantly binary (0/1) or tertiary (3/4/5) scores (Table 5).
Wings and
tail were composed of entirely pennaceous barbules on feather barbs,
characterized by the presence of hooklets on the
distal barbules, teeth on both distal and proximal barbules and variable
pigment on the rachis (Table 5; Image 6, 7). Body contour feathers were
composed of barbs containing purely pennaceous barbules, purely plumulaceous barbules and both plumulaceous
and pennaceous barbules (Image 8; Table 5). Semiplume
feathers were composed of barbs containing purely pennaceous barbules and barbs
containing purely plumulaceous barbules characterized
by the presence of villi, nodes, prongs, hooklets and
teeth (Image 9; Table 5). Down feathers (Image 10; Table 5), and powder down
(Image 11; Table 5) were composed of barbs containing plumulaceous
barbules characterized by presence of villi, nodes, and prongs. Two types of
nodal shape were noticed in down feathers opposed to only singular type in
powder down. Bristle feathers were characterized by presence of villi, nodes,
and prongs displaying characteristics nearer to non-contour feathers (Image 12;
Table 5).
DISCUSSION
Morphological
characteristics of various types of feathers were successfully studied in this
report. Primarily we found, feathers grouped under same types but from
different anatomical location have the exact same microscopic characteristics.
In this study we have provided such evidence after macro and micro level
examination of 350 slides prepared from 370 feather barbs obtained from 27
feathers sampled from an individual of Indian Pitta. Another study in such a systematic manner was
conducted by Chandler (1916) without any empirical data to it’s
annexure. About a century later in 2021, Ray and workers systematically
documented feather micro-characteristics of yellow billed babbler (Ray et al.
2021). Similarly in this study we have
successfully assessed and recorded the select feather characteristics of Indian
Pitta into empirical information. In this study we have successfully assessed
and recorded the selected parameters into empirical information.
The
identification of a unique barb in the dorsal body contour feathers for the
first time sheds light on possible subtle differences even in the same type of
feather but from different anatomical location. Though such a barb is an
exception as in all other cases we found that feathers grouped under same type
have exactly similar structure. Such a unique structure might be an adaptation
to its function. Having plumulaceous barbules and
pennaceous barbule in the same barb helps the feather in insulation as well as
in flight. Such a specialized barb might be a necessity for the dorsal feathers
that bear the blunt of air currents during a bird’s flight. Previous studies
displayed that passerines are generally characterized by the absence of
sub-pennaceous region (Lee et al. 2016), possibly the presence of newly
identified sub-plumulaceous region in dorsal body
contour feather barbs is specific to these birds. Although more studies
containing multiple passerine species from various families are needed to
authenticate such a hypothesis nevertheless the above discovery is unique enough
in its own right.
The bristle
feathers are believed to be structurally modified contour feathers in the
existing literature (Lovette & Fitzpatrick 2016).
However microscopic analysis in this study placed them structurally closer to
down and powder down feathers. The characteristics that separates bristle from
contour feather is the absence of ventral teeth and hooklets,
thus placing it closer to down and powder down types.
Correlation
between barb length and feather length was significant for down feathers only.
Such a correlation can be explained by the fact that length of down feather
barbs and length of down feathers are both essential to perform its function of
insulation and thermoregulation. Whereas, barb length and feather length of
other types of feather aren’t correlated enough in their functionality. Through
our study on the various feather types in Indian Pitta, we would like to
suggest that based on barbules, feather barbs can be divided broadly into three
types. These include: (i) barbs without any
sub-pennaceous or sub-plumulaceous region (in case of
Indian Pitta wing, tail, semiplume, down and powder
down feathers), (ii) feather containing barbs with sub-pennaceous or sub-plumulaceous region (sub-plumulaceous
region as present in body contour feathers from dorsal portion of Indian
Pitta), and (iii) feather containing barbs which are specially modified for
specific functions (bristle feathers). Such a morphology based classification
of barbs, can possibly be beneficial for designing feather related studies in
future.
Robertson
(Robertson et al. 1984) pointed that Chandler (1916) and Day (Day 1966) had
reported schemes for feather identification which lacked any corroborating
evidence. Also, the works of Hargrave (1965) and Messinger
(1965) were based on qualitative assessment of feather microstructures.
In 1984,
Robertson et al. (1984) quantified and provided numerical data of node density
and barbule length for consideration as species identification parameters;
however their data demonstrated that variation in barbule length and node
density within a species is considerably high and provides limited scope for
inter taxa identification. Same was also established by Joannah
Lee (Lee et al. 2016) through qualitative identification of feather micro
characteristics. Through our result we also state that, assessment of feather
microstructure qualitatively without any numerical data is capable of
differentiation between various types of feather.
The studies
of Robertson (1984) and Chandler (1916) state that pennaceous parts of contour
feather vary hugely amongst the feathers of same individual; however, through
our study we found that the pennaceous region of feathers of wings, tail, body
contour, and semiplume have exactly the same
microstructure, contradicting the findings of the previous studies. The
similarity in micro structures is expected as the feathers performing similar
functions are supposed to have exactly same microstructure. And as such the
similar trend is observed in all other feather types.
Previous
studies (Dove 1997b; Lee et al. 2016) have emphasized on the fact that an
appropriate reference collection, well trained staff and standardized
techniques is necessary for such feather related studies. Through our work we
have pioneered in such challenge for the first time in India and aim to create
a feather identification repository armed with trained personnel to perform
various feather investigations. Our study found that the technique of dry mount
followed by our study (Robertson et al. 1984; Lee et al. 2016) is best suited
for mounting feather barbs for observation under light microscope. The
technique of mounting the barb in medium (Dove & Coddington 2015) might
chaperone the delicate microstructures of villi and hooklets,
leading to faulty recording of observations. Systematic studies on feather
morphology helps us understand the form and functions of feathers better as
well as provide us better understanding of inter-species differences in feather
structures. The practical implications of our study can inculcate a whole range
of in-depth feather analysis as a tool for feather form and function
description or as a phylogenetic identification tool or as an aid in applied
wildlife forensic research.
Data
availability: Analyses reported in this
article can be reproduced using the data provided by the author upon acceptance
of the manuscript.
Table 1. Sampling details of
types of feather, location of feathers sampled, number of barbs sampled, slides
prepared, feather length in millimetre (mm) and mean
barb length in millimetre (mm).
|
Types of feather |
Location of feathers sampled |
No. of
barbs sampled |
Number of slides
prepared |
Length of
feather sampled (mm) |
Length of
barbs sampled (mm) |
|
|
|
|
|
|
|
mean |
±SE |
|
Contour |
Right Wing (Primary flight
feather) |
18 |
18 |
85.17 |
8.71 |
0.82 |
|
|
Right Wing (Secondary flight
feather) |
18 |
18 |
76.39 |
14.55 |
0.68 |
|
|
Left Wing (Primary flight
feather) |
18 |
18 |
87.32 |
8.52 |
0.68 |
|
|
Left Wing (Secondary flight
feather) |
18 |
18 |
76.10 |
13.70 |
0.75 |
|
|
Tail feather |
18 |
18 |
37.55 |
7.85 |
0.50 |
|
|
Body contour (Ventral) |
15 |
15 |
28.24 |
7.11 |
0.63 |
|
|
Body contour (Dorsal) |
15 |
15 |
24.86 |
9.50 |
0.14 |
|
|
|
|
|
|
|
|
|
Semiplume |
Ventral-1 |
15 |
15 |
33.66 |
7.88 |
0.35 |
|
|
Ventral-2 |
15 |
15 |
32.55 |
7.30 |
0.26 |
|
|
Near the tail |
15 |
15 |
29.59 |
9.32 |
0.53 |
|
|
Dorsal-1 |
15 |
15 |
36.59 |
9.04 |
0.49 |
|
|
Dorsal-2 |
15 |
15 |
27.69 |
7.83 |
0.68 |
|
|
|
|
|
|
|
|
|
Downy |
Dorsal |
15 |
15 |
23.42 |
9.56 |
0.22 |
|
|
Ventral |
15 |
15 |
10.24 |
5.19 |
0.22 |
|
|
Right wing |
15 |
15 |
10.67 |
5.72 |
0.13 |
|
|
Left wing |
15 |
15 |
12.53 |
5.94 |
0.25 |
|
|
Near tail |
15 |
15 |
11.74 |
5.83 |
0.38 |
|
|
|
|
|
|
|
|
|
Powderdown |
Right wing |
15 |
15 |
* |
4.99 |
0.19 |
|
|
Left wing |
15 |
15 |
* |
5.52 |
0.31 |
|
|
Ventral |
15 |
15 |
* |
9.48 |
0.40 |
|
|
Dorsal |
15 |
15 |
* |
5.11 |
0.16 |
|
|
Near tail |
15 |
15 |
* |
5.09 |
0.19 |
|
|
|
|
|
|
|
|
|
Bristle |
Orbital region and chin |
5 |
1 |
5.31 |
2.77 |
0.25 |
|
|
Orbital region and chin |
5 |
1 |
6.53 |
2.70 |
0.09 |
|
|
Orbital region and chin |
5 |
1 |
6.90 |
2.82 |
0.11 |
|
|
Orbital region and chin |
5 |
1 |
6.87 |
2.79 |
0.17 |
|
|
Orbital region and chin |
5 |
1 |
6.06 |
2.42 |
0.07 |
|
|
|
|
|
|
|
|
|
|
Total of 27 different feathers sampled |
Total of 370 Feather barbs sampled |
Total of 350
slides prepared |
|
|
|
* Length of powder down feathers
couldn’t be calculated due to very miniscule rachis and no particular
orientation of feather observed.
Table 2. Descriptive statistics
of sampled barbs from various types of feathers.
|
Types of feather |
No. of
barbs (N) |
Mean barb
length (mm) |
Range (mm) |
Coefficient
of variation (%) |
|
Wings |
72 |
11.37 ± 0.47 |
18.96–4.60 |
35.65 |
|
Tail |
18 |
7.85 ± 0.50 |
12.23– 4.65 |
26.65 |
|
Body contour |
30 |
8.31 ± 0.39 |
11.29–3.56 |
26.24 |
|
Semiplume |
75 |
8.27 ± 0.22 |
12.19–3.56 |
23.32 |
|
Down |
75 |
6.45 ± 0.21 |
10.75–4.03 |
28.34 |
|
Powderdown |
75 |
6.04 ± 0.23 |
12.00–3.31 |
33.10 |
|
Bristle |
25 |
2.70 ± 0.07 |
3.29–2.13 |
12.89 |
Table 3. Pearson correlation
coefficient of mean barb length and feather length of various feather types.
Confidence interval 95% (p ≤0.05).
|
|
Types of
feather |
|||||||
|
|
Contour |
Semiplume |
Down |
Bristle |
||||
|
|
r |
p - value |
r |
p - value |
r |
p - value |
r |
p - value |
|
Mean Barb length (mm) (α= 0.05, p ≤0.05) r= Pearson
correlation coefficient |
0.447 |
0.315 |
0.820 |
0.020 |
0.996 |
.000 |
0.287 |
0.640 |
Table 4. Details of macroscopic
characteristics observed in various feather types.
|
Type of feather |
Colour |
Texture of
barbs |
Pattern in
vanes |
Texture of
Rachis |
|
Wings |
Mostly black with patch of
white |
Stiff |
Bold |
Stiff |
|
Tail |
Mostly black with tinge of
green at one end |
Stiff |
Bold |
Stiff |
|
Body contour |
Black with cream/green colour
at one end |
Stiff, fluffy |
Bold |
Stiff |
|
Semiplume |
Whitish black, orange |
Stiff, fluffy |
Bold |
Stiff |
|
Down |
Mostly black with hints of grey |
Soft, fluffy |
Dull |
Soft |
|
Powder down |
Grey with black tinge |
Soft, fluffy |
Dull |
NA |
|
Bristle |
White with cream complexion |
Stiff |
Dull |
Stiffened &
strongly tapered towards one
end |
Table 5. Details of microscopic
characteristics observed in various feather types.
0—Absent | 1—Present | 3—Variable
| 4—Node shape flared on one side and diminished towards other | 5—Rod shaped
node | S/L—Small/Large | NA—Not applicable | D/P—Distal/Proximal barbule |
STR/KNK—Straight/Kinked.
|
Types of
feather |
Micro-characteristics
|
|||||||||||||||||
|
|
Sub-pennaceous
region |
Villi |
Nodes |
Node shape |
Prongs |
Presence of
prongs on both side of barb |
Prong size |
Hooklets |
Presence of
hooklets on both side of barb |
Teeth |
Presence of
teeth on both side of barb |
Internode
shape |
Pigmentation
|
|||||
|
|
0/1 |
0/1 |
0/1 |
|
0/1 |
0/1 |
D/P |
S/L |
0/1 |
0/1 |
D/P |
0/1 |
0/1 |
D/P |
STR/ KNK |
Nodes |
Inter-nodes
|
Ramu-s |
|
Wings |
0 |
0 |
0 |
NA |
0 |
NA |
NA |
NA |
1 |
0 |
D |
1 |
1 |
|
NA |
NA |
NA |
3 |
|
Tail |
0 |
0 |
0 |
NA |
0 |
NA |
NA |
NA |
1 |
0 |
D |
1 |
1 |
|
NA |
NA |
NA |
3 |
|
Body
contour |
0 |
1 |
1 |
4 |
1 |
1 |
|
S |
1 |
0 |
D |
1 |
1 |
|
STR |
1 |
3 |
3 |
|
Semiplume |
0 |
1 |
1 |
4 |
1 |
1 |
|
S |
1 |
0 |
D |
1 |
1 |
|
STR |
3 |
3 |
3 |
|
Down |
0 |
1 |
1 |
4,5 |
1 |
1 |
|
S |
0 |
NA |
NA |
0 |
NA |
NA |
STR |
3 |
3 |
3 |
|
Powderdown |
0 |
1 |
1 |
4 |
1 |
1 |
|
S |
0 |
NA |
NA |
0 |
NA |
NA |
STR |
3 |
3 |
3 |
|
Bristle |
0 |
1 |
1 |
4 |
1 |
1 |
|
S |
0 |
NA |
NA |
0 |
NA |
NA |
STR |
3 |
3 |
3 |
|
Repeated
barbs* |
0 |
1 |
1 |
4 |
1 |
1 |
|
S |
1 |
0 |
D |
1 |
1 |
|
STR |
1 |
3 |
3 |
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