Foram Planktonik Bentonik
Foram Planktonik Bentonik
edu/fosrec/)
Oleh
1. Sampling
2. Sampel
3. Metoda Preparasi
4. Peralatan Praktikum
5. Glossary
6. Morfologi Foraminifera
7. Kunci Identifikasi Genus dan Species Plangton Umur Plistosen - Resen
8. Kunci Identifikasi Genus dan Species Plangton Umur Kenozoikum
9. Kunci Identifikasi Genus dan Species Plangton Umur Mesozoikum
10. Kisaran umur beberapa marker plangton
11. Kunci Identifikasi Genus Bentonik
12. Diskripsi beberapa genus foraminifera plangton
13. Diskripsi beberapa genus foraminifera bentonik yang kosmopolitan di endapan Neogen
14. Foram Besar
15. Kisaran umur beberapa marker foram besar
16. Kunci Identifikasi Genus Kelompok Fusulinid.
17 Penyajian data
18. Interpretasi umur
19. Interpretasi lingkungan pengendapan
21. Non-Foram
22. Accessory Mineral
Panduan praktikum ini merupakan penjelasan singkat tentang parameter-parameter yang digunakan untuk
mengidentifikasi/mengklasifikasi atau mendiskripsi genus atau species foraminifera serta pedoman dalam
menginterpretasi umur dan lingkungan pengendapan berdasarkan foraminifera.
1. Sampling
Sistematika pengambilan sampel untuk analisa fosil foraminifera secara umum ada dua cara yaitu :
a. spot sampling;
b. sistematis sampling.
Sampel bisa berasal dari permukaan (surface outcrop) atau dari hasil pemboran.
2. Sampel
Ada empat macam sampel yang dikenal yaitu:
- Outcrop (sampel lapangan)
- dicth cutting )
- sidewall core (swc) ) dari hasil pemboran
- Core )
Masalah dalam interpretasi dapat disebabkan adanya fosil yang tidak in situ bisa karena reworked
(rombakan) atau displace/contaminant . Beberapa hal yang dapat menyebabkan kontaminasi adalah:
a. caving: yaitu material yang berasal dari lapisan yang lebih tinggi dalam suatu sumur pemboran, material
tersebut dapat dikenali dari ciri litologi yang sama yang telah terlihat diatasnya dalam satu sumur.
b. Recirculation: recirculation ini terjadi akibat adanya material/microfossil dari batuan yang telah dibor yang
kemudian ikut masuk kembali ke sumur bersama aliran lumpur pemboran dan kemudian berkontaminasi
dengan sampel yang ada.
c. Lost circulation material : kontaminasi berasal dari material pengisi rongga sumur pada waktu terjadi lost
circulation
d. Cement: semen untuk casing juga dapat mengandung foram yang dapat mengakibatkan kontaminasi
e. Drilling mud
Dari empat macam sjenis sampel dicth cutting merupakan sampel yang mempunyai karakter yang berbeda
(banyak mengandung contaminat) sehingga berbeda pula dalam interpretasinya. Sampel dari outcrop, swc
atau core akan memberikan gambaran lebih baik mengenai assosiasi fosil yang sebenarnya (in situ)
dibanding ditch cutting.
Jenis litologi juga harus diperhatikan dalam interpretasi, misal batupasir dilihat dari mekanisme
sedimentasinya jenis batuan ini merupakan hasil tranportasi, sehingga fosil yang berasosiasi dengan
batupasir harus dilihat dengaan hati-hati.
3. Metoda Preparasi
The techniques used to prepare and concentrate samples for examination vary according to rock type
(composition and grain size), how hard or resistant the sediment or rock is, how abundant the foraminifera
are, and how they are preserved within the sediment matrix. The discussions that follow focus on sediment
types that can be disaggregated in order to free the foraminiferal tests. This would include sands, silts and
clays, and the rock types produced when these sediments are hardened (sandstones, siltstones and shales,
respectively). For the hard limestone usually can be examination using thin section.
Foraminifera can be recovered from bulk sediment samples, although their presence or absence in any given
sample often cannot be established until after processing. The sampling strategy is simply to collect bags of
sediments/sedimentary rocks that can later be broken down and processed for foraminifera. Another
approach is to process sediment contained within larger fossils that one might collect. For example, the fossil
shells of marine snails and clams are often filled with the same sediment that surrounds them. Processing
these sediment fillings may yield foraminifera. Processing samples in the laboratory will require a source of
running water, a sieve, a funnel and some filter paper, and perhaps detergents or chemicals to help
disaggregate the sediments.
Precautionary Note: Make sure that labeling is carefully and accurately transcribed at every step. A
mislabeled sample has little, if any, scientific value.
a. Pencucian (Washing)
The object of all techniques described below is to isolate microfossils, in this case foraminifera, from the
sediment grains that surround them.Unconsolidated sediment and some soft rocks will break down after
Dirangkum oleh: Khoiril Anwar M
Lab. Mikropaleontologi, Jurusan Teknik Geologi ITB
1999
3
soaking in water for a few hours, whereas harder rocks may first require crushing and then boiling. The rule
of thumb here is to utilize the simplest and easiest technique that will provide the desired results. If simple
soaking is all that is required to disaggregate the sediment, then forego more involved techniques.
Regardless of which technique you utilize, initially breaking the sediment or rock into fragments several mm
in maximum dimension, or slightly larger, will speed the process.
Simple Soaking — If your sample is composed of unconsolidated sediment or sedimentary rock that can be
easily disaggregated, simple soaking may be all that is required. Soaking in distilled water is most desirable,
but using a dilute Calgon solution often helps to diaggregate fine sediments (muds). Calgon can be
purchased in the laundry detergent section of most grocery stores. This can be done in a large beaker or any
other clean glass container that is available. Experiment to see how long any given sample needs to be
soaked.
Once the muds have been dispersed, the sample can be washed through a sieve (a stainless steel U. S.
Standard Sieve No. 230 with mesh openings of 63 microns is recommended). Gently agitate your
water/sediment mixture, introduce it gradually onto the sieve, and wash under a gentle stream of water. Most
professionals recommend distilled water, but tap water may be used at this stage. The muds will pass
through the sieve and be discarded. Do not do this at a standard sink that is not equipped with a sediment
trap. If you do, you will have a clogged sink line in very short order. If you do not have a sink with a sediment
trap, do this outdoors or use a large bucket to catch what passes through the sieve. You can then dump
contents of the bucket outside. What remains on the sieve is a concentration of sand-sized material,
including any foraminifera that are in the sample. Rinse this material into filter paper placed within a funnel,
allow the sample to drain, and then air dry in place safe from contamination and breezes. When dry, the
grains should not adhere to one another. If they do, some mud still remains and the soaking/sieving
procedure should be repeated. When satisfactorily clean, the dried sample should be stored in a properly
labeled vial until ready for microscopic examination.
Don't get in a hurry during the sample processing phase. A bit of extra time invested in properly cleaning your
samples will save time and frustration when you examine them under the microscope.
Hydrogen Peroxide (H2O2) Method — If your sample is more resistant, additional treatments may be
required to breakit down. Soaking and, if necessary, boiling in a dilute solution of hydrogen peroxide is an
effective means of breaking down such samples (kadar peroksida yang digunakan jangan lebih dari 15
persen).
The steps in the H2O2 method are:
1) air-dry sample for several days or oven-dry sample for 24 hours at about 45°C;
2) place sample in 500-ml or 1000-ml pyrex beaker;
3) add fifteen percent hydrogen peroxide solution (volume of solution should be 2 to 3 times that of sample
being processed);
4) gently agitate and let soak for 24 hours at room temperature or in oven at about 45°C (stir occasionally
and keep covered to prevent contamination);
5) heat solution containing sample for 15 to 20 minutes, stirring frequently and taking care that the solution
does not boil over;
6) wash sample over No. 230 U. S. Standard Sieve as described earlier;
7) if sample is not disaggregated, transfer it back into beaker and repeat steps 3 through 6;
8) wash sample over No. 18 U.S. Standard Sieve (1-mm openings) and No. 230 U.S. Standard Sieve,
trapping coarser material on the No. 18 sieve and the sand fraction containing foraminifera on the No. 230
sieve (a coarse screen of the proper mesh size, available at any hardware store, can substitute for the No.
18 sieve);
9) dry and examine any material retained on the No. 18 sieve (not likely to be forams but may include other
fossils of interest);
10) transfer sample retained on No. 230 sieve to filter paper;
11) air-dry or oven-dry sample at 45°C;
12) transfer dried material to labeled vial for storage.
Other Techniques — Literature on the foraminifera describes other methods for disaggregating sediment
samples. A product called Quaternary O, a highly active but low sudsing detergent, was widely used for
many years (e.g., Snyder et al., 1983). Although it is no longer available, a product called Miramine is a
suitable and inexpensive substitute. It is available from the Miranol Chemical Company, 68 Culver Road,
Dayton, NJ 08810. The methodology for using surfactants such as Quaternary O or Miramine is exactly like
that desribed above for the use of hydrogen peroxide. Simply use the appropriately diluted detergent solution
in place of the H2O2 solution.
Another technique for additional cleaning involves use of a sodium pyrophosphate or a sodium
metaphosphate solution (e.g., Snyder and Waters, 1984). After an intial soaking (in distilled water or a dilute
Dirangkum oleh: Khoiril Anwar M
Lab. Mikropaleontologi, Jurusan Teknik Geologi ITB
1999
4
Calgon solution), the sand-sized residue trapped on the No. 230 sieve is placed in 0.1 M solution (five grams
of chemical to one liter of distilled water) and gently agitated for 20 to 30 minutes. This process effectively
removes persistent clay-sized particles that may partially obscure important features of the test.
Finally, some of the older literature, not cited here because the techniques may be extremely hazardous,
advocates the use of much harsher chemicals, including kerosene, gasoline, Varsol (similar to white gas or
mineral spirits), and concentrated H2O2. Use of these methods is not recommended because they can be
dangerous, both to the preparator and the environment.
CONCENTRATING THE TESTS OF FORAMINIFERA
Foraminiferal tests may be rare compared to nonbiogenic sediment particles. If foraminifera are reasonably
abundant, the best procedure is simple microscopic examination of the processed sample in order to find
them. However, there may be instances where the time required to examine the sample in this manner is
prohibitive. Then it may be desirable to float the foraminifera in order to separate them from other sediment
grains. The only reason this works is because foraminifera, with their hollow chambers, have an effective
density much less than solid sediment grains of comparable size. If the foraminifera are filled with sediment
or secondary mineral material, they will not float.
Soap Float — One of the simplest ways to concentrate foraminiferal tests is to employ a soap float. Here the
detergent is not of the low sudsing variety (such as Quaternary O), but rather a standard detergent or soap
that produces a sudsy froth. The processed sample is added in small increments to a solution of soap and
distilled water. With frequent agitation, the foraminifera become suspended in the surface froth while solid
sediment particles such as quartz grains sink to the bottom of the container. The froth can be periodically
decanted onto a No. 230 sieve and washed in a gentle stream of water to eliminate the suds. What remains
will be a concentration of foraminiferal tests, perhaps with some very fine sands of nonbiogenic origin. This
residue can be dried and examined under the microscope.
Other techniques can provide an even cleaner separation, but many involve the use of chemicals that are
extremely hazardous. For example, bromoform and carbon tetrachloride have been widely used to
concentrate foraminiferal tests by floating. However, both are carcinogenic and must be used under a fume
hood. The fumes are toxic and the chemicals can be absorbed through the skin. Consequently, use of these
chemicals to concentrate foram tests is not recommended. The use of another, safer chemical to accomplish
the same sort of separation is described below.
Flotation Using Sodium Polytungstate — Sodium polytungstate [also known as sodium metatungstate:
Na(H2W12O40)] is a non-toxic, high-density agent that is ecologically safe, easy to use, and recoverable so
that it may be re-used several times. It has a density of 3.1 g/ml, which can be reduced to any desired lesser
density simply by adding distilled water that is heated above 20°C. Although calcite has a density of 2.7 g/ml,
air is usually trapped within the foraminiferal tests making them more bouyant than quartz (density = 2.65
g/ml). For best results, the sodium polytungstate solution should be diluted until a piece of gypsum (density =
2.32 g/ml) floats and a piece of orthoclase (density = 2.57 g/ml) sinks. If the gypsum and orthoclase sink, the
liquid can be boiled off to increase the density.
Sodium polytungstate is available as a salt (in powder form) from GEOLIQUIDS, Inc., 15 E. Palatine Rd.,
Suite 109, Prospect Heights, IL 60070 and can be ordered by calling 1- 800-827-2411. The cost is about
$90.00/lb.
EXAMINING AND PICKING FORAMINIFERA
Processed samples, once dried, can be stored indefinitely in labeled vials until one desires to examine them.
The sample is then sprinkled sparsely across a picking tray and examined under a binocular microscope.
Brass picking trays with a grid of rectanglar subdivisions, all of equal size, are typically used by professionals.
The surface of the tray is a dull black (to minimize reflection) and the grid lines may be white or gold. Sources
for these trays are very difficult to find, but less sophisticated trays serve nicely. Any shallow plastic tray
measuring a few inches per side will suffice. If it is clear or highly lustrous, simply cut a piece of black
construction paper or cardboard to fit in the bottom of the tray. This will provide a background that will not
strain your eyes, and it provides a nice contrast to the foraminifera, which are typically white.
Any binocular microscope with reasonably good optics and the power to magnify 30 to 40 times will be
adequate for the study of foraminifera. Of course, scopes with better optics and magnifications up to 100
times are helpful.
Individual foraminiferal specimens encountered while examining samples strewn across the picking tray can
be picked and mounted for permanent reference. A recessed area in an 18-ply cardboard slide provides a
black background that can be coated with a water- soluble glue (e.g., Tragacanth). The cardboard slides will
also need glass cover slides and 18 ply aluminum holders.
Any foram specimens encountered on the picking tray can be captured using the wetted tip of an artist's
brush (buy size 000, sable hair). Simply dip the tip of the brush in water, touch it to the specimen you desire
Dirangkum oleh: Khoiril Anwar M
Lab. Mikropaleontologi, Jurusan Teknik Geologi ITB
1999
5
to pick, and transfer the specimen to the glued slide. The glue, being water soluble, will then dry and secure
the foram to the slide. At any time, wetting the specimen will release the glue so that the specimen may be
turned and viewed from different perspectives. A metal clip holds a glass cover slide over the cardboard
micropaleontology slide to protect specimens during prolonged storage. Using these slides, you can build a
reference collection of foraminifera to share with students.
You need to pick a set number of forams from the tray. In scientific studies 300 specimens (if the number of
preserved foram are avaliable) are usually picked. There is nothing magic in this number. It is an arbitrary
stopping point above which additional rare species are encountered more and more infrequently. Make sure
that you pick a representative suite of specimens. That is, do not pick only large specimens, or only small
ones, or only pretty ones. The best way to do this is to mark your picking tray with a numbered grid. Then
use a random numbers table to select a square. Pick all the specimens from that square and then select a
second square. Continue this process until your target number is reached and the specimens have been
transferred to a gum tragacanth-coated cardboard slide.
b. Sayatan tipis
Sayatan tipis umumnya ditujukan untuk pengamatan foram besar. Sayatan tersebut dapat berasal dari
sayatan batuan ataupun individu foram besar. Untuk batuan yang sangat kompak (indurated) biasanya
juga diamati dengan membuat sayatan tipis.
Ada beberapa cara untuk membuat sayatan pada individu foram besar:
4. Peralatan Praktikum:
- Mikroskop (reflected dan/atau transmited lights) + lampunya. Mikroskop jenis reflected light digunakan
untuk mengamati sampel hasil pencucian, sedang yang transmited light untuk pengamatan sampel dalam
bentuk sayatan tipis.
- Kuas kecil dan besar
- Pewarna
- Tray dengan dasar warna hitam dan bergaris (kotak)
- Slides (bisa lubang 1, 2, 3, 4 atau yang bernomor)
- Kertas dan pinsil
- micro-spliter
Catatan
Untuk mengambil (picking) dan menempelkan pada slide jangan memakai lem, tetapi dengan cara
membasahi kuas dengan ludah (dengan cara ujung kuas dikulum dalam mulut). Kalau menggunakan lem
akan susah untuk membolak-balik fosil bila sudah kering (fosil akan pecah dan lubang2 akan tertutup,
sedangkan air tidak akan menempelkan fosil dengan kuat (mudah lepas)). Penggunaan jarum akan membuat
fosil pecah atau loncat. Selama membolak-balik fosil gunakan kuas yang sudah dibasahi supaya fosil tidak
loncat dan tektur dinding kelihatan. Pewarna digunakan untuk melihat tektur dinding atau lubang apertur.
Berikut ini beberapa hal penting mengenai morfology test foraminifera. istilah-istilah bisa dilihat di glossary.
1. The basic building block of foraminifera tests consists of a cavity with a surrounding wall called a
chamber.
2. Although a few species consist of only a single chamber, most species are multi-chambered.
3. The simplest multi-chambered arrangement is a single linear series forming a uniserial test. Internally
the chambers are separated by walls called septa.
4. Externally a line or junction forms where the septa meet the chamber walls. This external line formed
between two chambers is called a suture.
5. In addition to a uniserial arrangement, biserial and triserial chamber arrangements are common.
6. Instead of forming a straight series of chambers, some foraminifera coil. Each volution in a coil (through
360 degrees) is called a whorl.
7. If the test coils in a single plane (that is, the chambers are centered on the plane), the coil is called
planispiral. Because of the bilateral symmetry, both sides of the test will appear identical.
8. If the test coils in a spire, like a snail, the coil is called trochospiral. A raised area in the center of a coil
is called an umbo and a depression, an umbilicus. A test in which earlier chambers become enveloped
by later ones is called involute. One in which chambers from a previous whorl are visible is called
evolute. In many trochospiral forms the spiral side is evolute and the umbilical side is involute. Some
foraminifera add their chambers in several planes.
9. A common arrangement in which five chambers are visible is called quinqueloculine.
10. Some Major evolutionary trends in coiling include Triserial to biserial to uniserial. However, some
lineages have reversable trends (e.g. Unilocular to multichambered to unilocular)
A. Organic (dimiliki oleh Suborder Allogromiina): umumnya merupakan dinding yang tidak rigid yang terbuat
dari bahan-bahan protein atau pseudochitin yang umumnya disebut tectin.
Dinding berkomposisi organic ini umumnya mudah hancur dan jarang menjadi fosil. Foraminifera dengan
cangkang berkomposisi organik banyak ditemukan pada lingkungan air tawar (fresh water foraminifera).
Contoh: Allogromia, Neogullmia
B. Gampingan (Calcareous):
Dinding gampingan ini umumnnya terdiri dari kristal-kristal kalsit dan aragonit, mempunyai berbagai
susunan/struktur yang berbeda satu sama lain, antara lain:
- porcelin ( dimiliki oleh Suboder Miliolina):
di mikroskop yang reflected: milky while (seperti porselen Cina)
di mikroskop yang transmited: amber colour (light brown)
Contoh: Quinqueloculina, Spiroloculina, Pyrgo.
(Brasier, 1980)
Dinding dari jenis hyaline dapat terdiri dari satu atau beberapa lapis, macamnya (Gambar 3):
non-laminar (= non-lamellar, meskipun sebenarnya istilah ini kurang tepat) : bila kamar berikutnya (kamar
baru) langsung nempel diatas kamar sebelumnya (tidak ada dinding kamar yang dilingkupi dengan dinding
kamar sebelumnya)
multilaminar bila dinding masing-masing kamar mempunyai beberapa lapisan, bisa berupa:
monolamelar: masing-masing kamar terdiri dari satu lapisan
bilamelar: masing-masing dinding kamar mempunyai konstruksi dasar yang terdiri dari dua lapisan
Penting untuk diperhatikan adalah jumlah kamar, terutama jumlah kamar pada putaran terakhir, bila kamar-
kamarnya terputar.
(Brasier, 1980)
(Brasier, 1980)
gross shape (profil):
Profil test foraminifera bisa dideskripsi secara umum, atau dilihat dari salah satu sisi, misal dari periheral
(samping), dorsal (sisi spiral) atau ventral (sisi umbilicus). Bentuk profil test (cangkang) tersebut antara lain
(Gambar 5, 6): planoconvex (spiroconvex dan umbilicoconvex), biconvex/lenticular, globular, spherical,
stellate, discoidal, fusiform, trihedral, palmate (i.e. Frondicularia), sagitate (ie. Bolivina) , flabiliform (i.e.
Pavonina), dll.
(Brasier, 1980)
Gambar 4 perkembangan test yang multilocular
1a 1b 1c 1d
(Stainforth, 1972)
Gambar 11 Bentuk modifikasi apertur
6.5 Sutura:
Sutura merupakan pertemuan antar kamar atau antar putaran, dapat dibedakan dari bentuknya, apakah :
lurus (straight), arcuate (lengkung), sinusous (bergelombang) dan karakternya: flush, depresed, incised,
beaded. Seringkali sutura foraminifera menebal dan biasa disebut sebagai limbate.
(Catatan: Parameter ini harus hati2 jika digunakan untuk parameter identifikasi karena mereka bervariasi
pada tahap ontogeni dan juga terpengaruh oleh lingkungan)
6.7 Umbilicus
Parameter lain yang sering digunakan untuk diskripsi adalah umbilicus yaitu axial area yang mana dari sisi
ini kamar2 tampak memencar (radiate). Umbilicus bisa tertutup (closed : terlihat hanya sebagai titik dimana
sutura bertemu) atau narrowly deep ( bentuk seperti pinhole: lubang kecil dan panjang) bentuk2 tersebut
umumnya dimiliki oleh yang mempunyai putaran ketat; bentuk lain dari umbilicus adalah terbuka.
6. 9 Ukuran:
Termasuk ukuran diameter dan panjang atau tinggi. Jika mungkin ukuran dari proloculus dan kecepatan
peningkatan ukuran dan diameter kamar serta putaranya.
Sejauh ini paramenter 1 s/d 4 adalah yang paling penting didalam taxonomi foraminifera (dalam
panduan ini, parameter 6.1 s/d 6.9). Parameter/unsur-unsur tersebut harus diperhatikan dalam
mengamati atau mendiskripsi fosil foraminifera, terutama pada foraminifera kecil. Pengamatan pada
foraminifera besar lebih komplek meskipun pada dasarnya parameternya hampir sama.
Dalam mendiskripsi suatu fosil hendaknya mengikuti aturan tertentu (lihat contoh diskripsi) dan
usahakan sejelas mungkin.
I. Test surface rough under light microscope (spine, spine bases, granules, pustuloses):
A. Spine visible on living or well-preserved specimens; spine-bases on most specimens, located
interporate area [Hastigerinnidae; Globigerinidae]
1. Spines or spine bases restricted to distal end of chambers [Hastigerinidae]
a. globular to subglobular chamberss, planispiral coiling [Hastigerina], species:H. pelagica,
parapelagica
b. clavate chambers, streptospiral coiling [Hastigerinopsis], species: H. digitiformans
2. Spines or spine baseson all portion of test wall [Globigerinidae]
a. primary aperture only
a.1 radially elongate chambers
low trochospire: [Globigerinella], species: G. adamsi, aequilateralis, calida
mediumtrochospire or streptosspire [Bella], species: B. digitata
a.2 globular or sperical chambers [Globigerina], species: G. antartica, bernudezi, bulloides,
decoraperta, falconensis, quinquiloba, umbilicata
b. suplementary aperture present
b.1 sperical to subbglobular chambers
singgle spherical chambers [Orbulina], species O universa, suturalis
subglobular chambers [Sphaeroidinella], sspecies: S. dehiscens, excavata
subglobular - spherical chambers [Globigerinoides], species: conglobatus, elongatus,
fistulosus, obliquus, pyramidalis, ruber, sacculifer
B. Pustules or granules visible under light microscope on test surface, no spines or spine bases
[ globorotalidae]
1. Surface granular, coarsely pitted
a. pustules present only near aperture
Apertural tooth present [Globoquadrina], species: G. conglomerata, pseudofoiliata
No apertural tooth [Globorotaloides], species: G.hexagona
b. pustules not prominent (generally with apertural tooth) [Neogloboquadrina] low to medium
trochospire; species N. asonoi, blowi, eggeri, humerosa, pachyderma, pseudohumerosa,
himiensis
medium to high trochospire, species: dutertrei
2. Surface pustulate
a. peripheral keel absent
Singular pustules [Globorotalia], species: hirsuta, inflata, oceanica, scitula, tosaensis, hessi,
ronda;
Multiple pustules[Neocarinina], species: N. blowi
b. peripheral keel present [Globorotalia (keeled)], species: frimbiata, flexuosa, menardii, tumida,
pertenuis, theyeri, truncatulinoides, cultrata ungulata, viola
4. Test pada putaran awal trochospiral, putaran akhir atau kamar akhir melingkupi sebagian atau seluruh
kamar putaran sebelumnya
4.1 tanpa bulla
4.1.1 seperti globigerina, putaran akhir atau kamar akhir melingkupi sebagian umbilical dengan
aperture tambahan pada sutura melingkupi umbilical ruang = Globigerapsis
Dirangkum oleh: Khoiril Anwar M
Lab. Mikropaleontologi, Jurusan Teknik Geologi ITB
1999
22
4.1.2 seperti globigerinoides dengan kamar akhir mempunyai aperture tambahan pada sutura yang
melingkupi umbilical ruang = Orbulinoides atau Praeorbulina
4.1.3 seperti globigerina dengan kamar akhir seluruh atau hampir seluruhnya melingkupi kamar pada
putaran sebelumnya; aperture sepanjang sutura dan aerial aperture pada kamar akhir =
Orbulina
4.2 dengan bulla
4.2.1 seperti globigerina, putaran akhir atau kamar akhir membulat menutupi umbilicus, mempunyai
aperture tambahan pada sutura yang ditutupi oleh bulla sempit ( tiap bulla punya lubang
infralaminal) = Globigerinatheka
4.2.2 seperti globigerinatheka, sutura lebih tak teratur; aperture multiple tersebar pada kamar akhir
yang ditutupi oleh bulla; bulla appressed, bervariasi menutupi sebagian besar test , tiap bulla
mempunyai lubang infralaminal (infralaminal aperture) sepanjang tepi-tepinya =
Globigerinatella
4.3 dengan atau tanpa bulla
putaran awal seperti globigerina, putaran akhir terdiri 2 atau 3 kamar yang berpukan erat, stuktur
dinding komplek terdiri dari lebih satu lapisan kulit meterial. aperture slit-like atau iregular
4.3.1 hanya punya satu apertuer = Sphaeroidinellopsis
4.3.2 punya dua atau lebih apertur = Sphaeroidinella
5. Test pada putaran awal trochospiral menjadi streptospiral pada putaran akhir; pada putaran awal umbilicus
terbuka, pada putaran akhir tanpa ada umbilicus = Pulleniatina
6. Test streptospiral, kamar clavate, radial elongated, pada pertumbuhan selanjutnya menjadi bifurcating
atau trifurcating = Hastigerinella
1. Test trochospiral
1.1 primary aperture umbilical-extraumbilical
1.1.1-with sutural suplementary apertures at umbilical: (Rotaliporinae):
-chamber sperical, without keel : Ticinella
-with keel : Rotalipora
1.1.2-without suplementary aperture at umbilical
-without keel: (Hedbergellinae)
-with lip
-without relict aperture at spiral side: Hedbergella
-with relict aperture at spiral side: Loeblichella
-with tegilla and infralaminal ap. acc.: Globotruncanella
-with 1 or 2 keel (composed of : pustules and/or imbrication): (Marginotruncaninae)
-radial sutura, depressed at umbilical side
- with lip or portici
- 1 keel : Praeglobotruncana
- 2 keel : Dicarinella
- with tegila and infra and intralaminal aperture accesory:Abathomphalus
-sutura sigmoid at umbilical side, 2 keel : Marginotruncana
2. Test early portion trochospiral, later planispiral, aperture extraumbilical, tending to become equatorial:
- chaamber elongated, with a hollow bulb-shape or spine-like extention in equatorial plane: Schackoina
- chambers elongated, some or all chambers of the last whorl with two or ccasionally more, hollow bulb-
shape extention on each side of the equatorial plane: Leupoldina
3. Test planispiral
-Primary aperture equatorial bordered by a lip, with relict aperture:
- with keel: Planomalina
- without keel:
-chambers globular to ovate: Globigerinelloides
-chambers radial-ellongate : Hastigerinoides
M L E AR L Y MID D L E L ATE
P19 P20 P21 P22 N4 N5 N6 N7 N8 N9 N10 N11 N12 N13 N14 N15 N16 N17 N18 N19 N20 N21 N22 N23
Glo bige rina c alida c alida
Glo bo ro talia to s ae ns is
Glo bo ro talia fo hs i fo hs i
Glo bo ro talia fo hs i lo bata
M L E AR L Y MID D L E L ATE
P19 P20 P21 P22 N4 N5 N6 N7 N8 N9 N10 N11 N12 N13 N14 N15 N16 N17 N18 N19 N20 N21 N22 N23
Glo bige rino ide s prim o rdius
Glo bige rina o uac hitae ns is c ipe ro e ns is
Glo bo ro talia k ugle ri
Glo bige rina angulis uturalis
Glo bige rina tripartita
Glo bige rina s e llii
Glo bige rina go rtanii
Glo bo ro talia o pim a nana
Glo bo ro talia o pim a o pim a
Glo bige rina galav is i
Glo bige rina pras ae pis P ulle niatina finalis
Glo bige rina o ffic inalis Glo bige rina dute rtrei
Glo bige rina am pliape rtura Glo bo ro talia frim biata
Glo bige rina tapurie ns is Glo bige rina rube s c e ns
P s e udo has s tige rina m ic ra S phae ro idine lla dehis c ens dehis c e ns
Glo bo ro talia inc re bes c e ns Glo bo ro talia ungulata
ge rina ps e udo am pliape rtura P ulle niatina o blique lo c ulata
Glo bige rino ide s fis tulo s us
Glo bige rino ide s c o nglo batus
Glo bo ro talia tum ida tum ida
Glo bo ro talia hum e ro s a
Glo bo ro talia cras s afo rm is s .l.
P19 P20 P21 P22 N4 N5 N6 N7 N8 N9 N10 N11 N12 N13 N14 N15 N16 N17 N18 N19 N20 N21 N22 N23
Cassigerinella : Small involute biserial (cassiduline) coil of inflated chambers; aperture a simple arch
directed alternately to right and left on successive chambers.
Cribrohantkenina: Test as in Hantkenina with strongly inflated chambers and larger apertural face on which
arched aperture is suplemented or replaced by one or more rows of larger apertural pore.
Globigerina: Trochospire of globose to ovate chambers, variying greatly in coiling parameters but
characterized by its aperture, which is a simple opening into the umbilicus.
Globigerinoides: An umbilicate trochospire as in Globigerina but at least one (and generally several)
supplementary aperture on spiral side, these apertures range from small gap where sutures intersect
to conspicious lunate opening along spiral suture.
Globorotalia: Test vary variable but basicaly a reguler trochospire of closely packed, gradually enlargering
chambers, aperture a slit or arch between umbilicus and peripheri, directed forward rather than inward,
commonly with some form of rim, lip or flange.
Globigerinita: Test a Globigeria-like trochospire but umbilical pit is covered by a bulla: shell delicate,
smooth, matte surface, few to many infralaminal opening may surround bulla.
Globoquadrina: Test as in Globigerina except that each aperture carries a flap with ranges from a narrow
flange to an elaborate trianglar tooth.
Hanktenina: Regular planispiral coil, commonly involute, suture straight, radial, and deeply incised,
chambers apiculate to triangular and bearing distinctive spine at tips; aperture a highly arched slit that
may be bordered by alips or flanges.
Hastigerina: Planispiral coil of bulbous to elongated chambers; aperture an arch or slit embracing inner coil.
Immature and primitive may have trochospiral tendency.
Orbulina: Test sperical with only final chamber or final chamber with small part of initial spire ( flush with or
protuding slightly throught sperical surface) visible.
Neogloboquadrina: Test trochospiral, chamber shape ovate to subglobular, wall calcareous, perforate,
primary aperture umbilical, aperture modifications typically present, such as teeth; no secondary
aperture
Pulleniatina: Test streptospiral, chamber subglobular, wall calcareous, adult have thick cortex, primary
apertureinteriomarginal umbilical-extraumblical, no secondary aperture.
Praeorbulina: Initially low trochospiral but become globular to sperical beecouse of rapidly increasing size
and enveloping nature of adult chambers; final chamber cover 40 - 70% of earlier test. No primary
aperture in adult stage, but numeros slit or larger pore along suture of last chamber.
Sphaeroidinella: Test trochospiral; chamber globular; wall calcareous, perforate covered with heavy cortex;
primary aperture umbilical. largerly obscure by overhanging cortex turing outwards forming chamber
flanges; secondary (s) aperture located on spiral side.
Sphaeroidinellopsis: Trochospiral, ranging from loose and umbilicate to appessed, ovoid, with umbilical slit,
characterized by thick, impervorate to vitreous cortex that overlies primary perforate wall test. no
secondary aperture
32
13. Diskripsi Genus-genus foraminifera bentos yang kosmopolitan pada endapan Neogen di
Indonesia:
Ammonia : test calcareous, low trochospiral 3-4 putaran, suture slightly curved, thicknes, depressed on
umbilical side, umbilical surface with irregular granulanes along suture and over umbilical region,
umbilicus with open umbilical fissure and plug.
Anomalinella: test planispiral involute; lenticular; wall coarse perfotare with peripheral keel; aperture low,
rounded interomarginal arch, bordered by lip.
Anomallina: test low trochospiral or nearly planispiral; spiral side with umbonal bos, oppsite site with
depressed umbilicus; aperture interomarginal equatorial opening extending to umbilical side.
Asterorotalia: test trochospiral, biconvex, with 3 prominent slender spine radiating from test, margin
carinate.
Bigenerina: early test biserial become uniserial, wall aglutinanted; aperture terminal rounded.
Bolivina: biserial, retral processes, aperture narrow elongate loop up chamber face with toothplate
Bulimina: triserial, aperture bentuk koma
Cancris: test trochospiral; biconvex; elongated and auriculte in shape; chamber rapidly enlarging; may have
peripheral keel and apertural lip. ( differs from Baggina in being more elongated, evolute in spiral side,
keeled and in having an open umbilicus and an apertural lip)
Cassidulina: biserial terputar; lenticular; aperture elongated slit curve pararel to anterior margin of chamber
with narrow lip
Cellanthus: seperti elphidium tetapi mempunyai biumbilical bos
Cibicides: low trochospiral; dorsal flat; umbilical convex; peripheri angular with keel
Cyclamina: test palnispiral involute; wall aglutinant; wall and septa strongly labyrinthic; aperture equatorial
slit and numerous pore scatered over face.
Dentalina: test elongate; arcuate; uniserial; suture oblique; aperture radiate, terminal
Discorbis: test trochospiral biconvex; plano-convex; flatened on umbilical side; periphery angled; umbilical
with flap; primary aperture extraumbilical, secondary sutural opening at opposide of chamber flap
Elpidium: test planispiral involute; chamber numerous with retral processes; wall calcareous; surface
commonly with groves or ridges pararelling periphery.
Fissurina: test rounded or ovate in outline; compressed trigonal or tetragonal in section, and may keeled,
surface smooth, costate, beaded; aperture slitlike to oval or rounded
Florilus: test planispiral bbut may be asymetrical, involute; chambers increasing rapidly in breadth and
thickness resulting in flaring test; aperture narrow equatorial opening.
Frondicularia: test elongated or palmae; flatened; chamber low broad and equitant; suture strongly arched
or angled at center of test; aperture terminal radiate may have short neck.
Gyroidina: test trochospiral, planoconvex; periphery rounded to subtruncate; primary aperture a low
interomarginal slit restricted to mid-portion of apertural face bordered by narrow lip.
Haplophragmoides: test planispiral involute; wall aglutinanted; aperture equatorial slit.
Heterolepa: test trochospiral, planoconve; periphery bluntly angled, may have keel; slowly enlargering
chamber; aperture interomarginal slitlike at extraumblical to peripheri on spiral side.
Hoeglundina: test trochospiral, lenticular, perpheri angular to carinete; umbilical area closed; suture
thickened may be elevated; aperture lateromarginal opening pararelling pheriphery on umbilical side.
Lagena: test unilocular (monothalamus), rarely 2 or more chambers; aperture on elongated neck which may
have phyaline lip, not radiate.
Lenticulina: test planispiral; lenticular; biumbonate; aperture radial at peripheral angle
Marginulina: early portion coiled but not completly enroled as in Marginulinopsis later rectilinear; suture
oblique; aperture dorsal angled
Melonis: test early stage slitghly trochospiral, adult planispiral simetri and involute; biumbilicate with
umbilicus bordered by rim; perihery broadly rounded; apertural face, septa and umbilical thickened rim
imperforate; aperture equatorial slit extending to umbilical in both side.
Nodosaria: test multilocular; rectilinear; rounded in section; aperture terminal,central basically radiate may
be produce on neck
Oolina: test single globular to ovate chamber; aperture rounded and may have radiating groves surrounding
aperture on exterior.
Oridorsalis: test trochospiral, lenticular; periphery carinate; suture radial in spiral side and strongly sinusoid
in umbilical side.
Planulina: test low trochospiral, discoidal; peripheri truncate with thick marginal imperforate keel; suture
strongly arched, thickened, nonperforate; aperture an equatorial arch with narrow bordering lip.
Pseudorotalia: test trochospiral, periphery acute with imperforate keel; chambers with imperforate umbilical
lips confined to radial sector and with imperforate plate-like extentions formed by each succeding
chamber lamella covering umbilical area; cameral aperture interiomarginal on umbilical side, apertual