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Introduction to Networks v6
Companion Guide
Cisco Networking Academy

800 East 96th Street

Indianapolis, Indiana 46240 USA
Introduction to Networks v6 Companion
Guide
Cisco Networking Academy
Copyright © 2017 Cisco Systems, Inc.
Published by:
Cisco Press
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About the Contributing Authors
Rick Graziani teaches computer science and computer networking
courses at Cabrillo College in Aptos, California. Prior to teaching Rick
worked in the information technology field for Santa Cruz Operation,
Tandem Computers, Lockheed Missiles and Space Corporation, and served in
the U.S. Coast Guard. He holds an M.A. in Computer Science and Systems
Theory from California State University Monterey Bay. Rick also works as a
curriculum developer for the Cisco Networking Academy Curriculum
Engineering team. When Rick is not working, he is most likely surfing at one
of his favorite Santa Cruz surf breaks.
Allan Johnson entered the academic world in 1999 after 10 years as a
business owner/operator to dedicate his efforts to his passion for teaching. He
holds both an MBA and an M.Ed. in Occupational Training and
Development. He taught CCNA courses at the high school level for seven
years and has taught both CCNA and CCNP courses at Del Mar College in
Corpus Christi, Texas. In 2003, Allan began to commit much of his time and
energy to the CCNA Instructional Support Team, providing services to
Networking Academy instructors worldwide and creating training materials.
He now works full time for Cisco Networking Academy as a Curriculum
Developer.
Contents at a Glance
Introduction
Chapter 1 Explore the Network
Chapter 2 Configure a Network Operating System
Chapter 3 Network Protocols and Communications
Chapter 4 Network Access
Chapter 5 Ethernet
Chapter 6 Network Layer
Chapter 7 IP Addressing
Chapter 8 Subnetting IP Networks
Chapter 9 Transport Layer
Chapter 10 Application Layer
Chapter 11 Build a Small Network
Appendix A
Glossary
Index
Contents
Introduction
Chapter 1 Explore the Network
Objectives
Key Terms
Introduction (1.0.1.1)
Globally Connected (1.1)
Networking Today (1.1.1)
Networks in Our Daily Lives (1.1.1.1)
Technology Then and Now (1.1.1.2)
No Boundaries (1.1.1.3)
Networks Support the Way We Learn (1.1.1.4)
Networks Support the Way We Communicate (1.1.1.5)
Networks Support the Way We Work (1.1.1.6)
Networks Support the Way We Play (1.1.1.7)
Providing Resources in a Network (1.1.2)
Networks of Many Sizes (1.1.2.1)
Clients and Servers (1.1.2.2)
Peer-to-Peer (1.1.2.3)
LANs, WANs, and the Internet (1.2)
Network Components (1.2.1)
Overview of Network Components (1.2.1.1)
End Devices (1.2.1.2)
Intermediary Network Devices (1.2.1.3)
Network Media (1.2.1.4)
Network Representations (1.2.1.5)
Topology Diagrams (1.2.1.6)
LANs and WANs (1.2.2)
 Types of Networks (1.2.2.1)
Local Area Networks (1.2.2.2)
Wide Area Networks (1.2.2.3)
The Internet, Intranets, and Extranets (1.2.3)
The Internet (1.2.3.1)
Intranets and Extranets (1.2.3.2)
Internet Connections (1.2.4)
Internet Access Technologies (1.2.4.1)
Home and Small Office Internet Connections (1.2.4.2)
Businesses Internet Connections (1.2.4.3)
The Network as a Platform (1.3)
Converged Networks (1.3.1)
Traditional Separate Networks (1.3.1.1)
The Converging Network (1.3.1.2)
Reliable Network (1.3.2)
Network Architecture (1.3.2.1)
Fault Tolerance (1.3.2.2)
Scalability (1.3.2.3)
Quality of Service (1.3.2.4)
Security (1.3.2.5)
The Changing Network Environment (1.4)
Network Trends (1.4.1)
New Trends (1.4.1.1)
Bring Your Own Device (1.4.1.2)
Online Collaboration (1.4.1.3)
Video Communication (1.4.1.4)
Cloud Computing (1.4.1.5)
Networking Technologies for the Home (1.4.2)
Technology Trends in the Home (1.4.2.1)
Powerline Networking (1.4.2.2)
 Wireless Broadband (1.4.2.3)
Network Security (1.4.3)
Security Threats (1.4.3.1)
Security Solutions (1.4.3.2)
Network Architecture (1.4.4)
Cisco Network Architecture (1.4.4.1)
CCNA (1.4.4.2)
Summary (1.5)
Warriors of the Net (1.5.1.2)
Conclusion (1.5.1.3)
Practice
Class Activities
Labs
Packet Tracer Activities
Check Your Understanding Questions
Chapter 2 Configure a Network Operating System
Objectives
Key Terms
Introduction (2.0.1.1)
IOS Bootcamp (2.1)
Cisco IOS (2.1.1)
Operating Systems (2.1.1.1)
Purpose of OS (2.1.1.2)
Cisco IOS Access (2.1.2)
Access Methods (2.1.2.1)
Terminal Emulation Programs (2.1.2.2)
Navigate the IOS (2.1.3)
Cisco IOS Modes of Operation (2.1.3.1)
Primary Command Modes (2.1.3.2)
Configuration Command Modes (2.1.3.3)
 Navigate Between IOS Modes (2.1.3.4)
The Command Structure (2.1.4)
Basic IOS Command Structure (2.1.4.1)
IOS Command Syntax (2.1.4.2)
IOS Help Features (2.1.4.3)
Hotkeys and Shortcuts (2.1.4.4)
Basic Device Configuration (2.2)
Hostnames (2.2.1)
Device Names (2.2.1.1)
Configure Hostnames (2.2.1.2)
Limit Access to Device Configurations (2.2.2)
Secure Device Access (2.2.2.1)
Configure Passwords (2.2.2.2)
Encrypt Passwords (2.2.2.3)
Banner Messages (2.2.2.4)
Save Configurations (2.2.3)
Save the Running Configuration File (2.2.3.1)
Alter the Running Configuration (2.2.3.2)
Capture Configuration to a Text File (2.2.3.3)
Address Schemes (2.3)
Ports and Addresses (2.3.1)
IP Addresses (2.3.1.1)
Interfaces and Ports (2.3.1.2)
Configure IP Addressing (2.3.2)
Manual IP Address Configuration for End Devices (2.3.2.1)
Automatic IP Address Configuration for End Devices (2.3.2.2)
Switch Virtual Interface Configuration (2.3.2.3)
Verifying Connectivity (2.3.3)
Interface Addressing Verification (2.3.3.1)
End-to-End Connectivity Test (2.3.3.2)
 Summary (2.4)
Practice
Class Activities
Labs
Packet Tracer Activities
Check Your Understanding Questions
Chapter 3 Network Protocols and Communications
Objectives
Key Terms
Introduction (3.0)
Rules of Communication (3.1)
The Rules (3.1.1)
Communication Fundamentals (3.1.1.1)
Rule Establishment (3.1.1.2)
Message Encoding (3.1.1.3)
Message Formatting and Encapsulation (3.1.1.4)
Message Size (3.1.1.5)
Message Timing (3.1.1.6)
Message Delivery Options (3.1.1.7)
Network Protocols and Standards (3.2)
Protocols (3.2.1)
Rules that Govern Communications (3.2.1.1)
Network Protocols (3.2.1.2)
Protocol Interaction (3.2.1.3)
Protocol Suites (3.2.2)
Protocol Suites and Industry Standards (3.2.2.1)
Development of TCP/IP (3.2.2.2)
TCP/IP Protocol Suite (3.2.2.3)
TCP/IP Communication Process (3.2.2.4)
Standard Organizations (3.2.3)
 Open Standards (3.2.3.1)
Internet Standards (3.2.3.2)
Electronics and Communications Standard Organizations (3.2.3.3)
Reference Models (3.2.4)
The Benefits of Using a Layered Model (3.2.4.1)
The OSI Reference Model (3.2.4.2)
The TCP/IP Protocol Model (3.2.4.3)
OSI Model and TCP/IP Model Comparison (3.2.4.4)
Data Transfer in the Network (3.3)
Data Encapsulation (3.3.1)
Message Segmentation (3.3.1.1)
Protocol Data Units (3.3.1.2)
Encapsulation Example (3.3.1.3)
De-encapsulation (3.3.1.4)
Data Access (3.3.2)
Network Addresses (3.3.2.1)
Data Link Addresses (3.3.2.2)
Devices on the Same Network (3.3.2.3)
Devices on a Remote Network (3.3.2.4)
Summary (3.4)
Practice
Class Activities
Labs
Packet Tracer Activities
Check Your Understanding Questions
Chapter 4 Network Access
Objectives
Key Terms
Introduction (4.0)
Physical Layer Protocols (4.1)
 Physical Layer Connection (4.1.1)
Types of Connections (4.1.1.1)
Network Interface Cards (4.1.1.2)
Purpose of the Physical Layer (4.1.2)
The Physical Layer (4.1.2.1)
Physical Layer Media (4.1.2.2)
Physical Layer Standards (4.1.2.3)
Physical Layer Characteristics (4.1.3)
Functions (4.1.3.1)
Bandwidth (4.1.3.2)
Throughput (4.1.3.3)
Types of Physical Media (4.1.3.4)
Network Media (4.2)
Copper Cabling (4.2.1)
Characteristics of Copper Cabling (4.2.1.1)
Copper Media (4.2.1.2)
Unshielded Twisted-Pair Cable (4.2.1.3)
Shielded Twisted-Pair Cable (4.2.1.4)
Coaxial Cable (4.2.1.5)
Copper Media Safety (4.2.1.6)
UTP Cabling (4.2.2)
Properties of UTP Cabling (4.2.2.1)
UTP Cabling Standards (4.2.2.2)
UTP Connectors (4.2.2.3)
Types of UTP Cable (4.2.2.4)
Testing UTP Cables (4.2.2.5)
Fiber-Optic Cabling (4.2.3)
Properties of Fiber-Optic Cabling (4.2.3.1)
Fiber Media Cable Design (4.2.3.2)
Types of Fiber Media (4.2.3.3)
 Fiber-Optic Connectors (4.2.3.4)
Testing Fiber Cables (4.2.3.5)
Fiber versus Copper (4.2.3.6)
Wireless Media (4.2.4)
Properties of Wireless Media (4.2.4.1)
Types of Wireless Media (4.2.4.2)
Wireless LAN (4.2.4.3)
Data Link Layer Protocols (4.3)
Purpose of the Data Link Layer (4.3.1)
The Data Link Layer (4.3.1.1)
Data Link Sublayers (4.3.1.2)
Media Access Control (4.3.1.3)
Providing Access to Media (4.3.1.4)
Data Link Layer Standards (4.3.1.5)
Media Access Control (4.4)
Topologies (4.4.1)
Controlling Access to the Media (4.4.1.1)
Physical and Logical Topologies (4.4.1.2)
WAN Topologies (4.4.2)
Common Physical WAN Topologies (4.4.2.1)
Physical Point-to-Point Topology (4.4.2.2)
Logical Point-to-Point Topology (4.4.2.3)
LAN Topologies (4.4.3)
Physical LAN Topologies (4.4.3.1)
Half and Full Duplex (4.4.3.2)
Media Access Control Methods (4.4.3.3)
Contention-Based Access – CSMA/CD (4.4.3.4)
Contention-Based Access – CSMA/CA (4.4.3.5)
Data Link Frame (4.4.4)
The Frame (4.4.4.1)
 Frame Fields (4.4.4.2)
Layer 2 Address (4.4.4.4)
LAN and WAN Frames (4.4.4.5)
Summary (4.5)
Practice
Class Activities
Labs
Packet Tracer Activities
Check Your Understanding Questions
Chapter 5 Ethernet
Objectives
Key Terms
Introduction (5.0)
Ethernet Protocol (5.1)
Ethernet Frame (5.1.1)
Ethernet Encapsulation (5.1.1.1)
MAC Sublayer (5.1.1.2)
Ethernet Evolution (5.1.1.3)
Ethernet Frame Fields (5.1.1.4)
Ethernet MAC Addresses (5.1.2)
MAC Address and Hexadecimal (5.1.2.1)
MAC Address: Ethernet Identity (5.1.2.2)
Frame Processing (5.1.2.3)
MAC Address Representations (5.1.2.4)
Unicast MAC Address (5.1.2.5)
Broadcast MAC Address (5.1.2.6)
Multicast MAC Address (5.1.2.7)
LAN Switches (5.2)
The MAC Address Table (5.2.1)
Switch Fundamentals (5.2.1.1)
 Learning MAC Addresses (5.2.1.2)
Filtering Frames (5.2.1.3)
MAC Address Tables on Connected Switches (5.2.1.4)
Sending a Frame to the Default Gateway (5.2.1.5)
Switch Forwarding Methods (5.2.2)
Frame Forwarding Methods on Cisco Switches (5.2.2.1)
Cut-Through Switching (5.2.2.2)
Memory Buffering on Switches (5.2.2.3)
Switch Port Settings (5.2.3)
Duplex and Speed Settings (5.2.3.1)
Auto-MDIX (5.2.3.2)
Address Resolution Protocol (5.3)
MAC and IP (5.3.1)
Destination on Same Network (5.3.1.1)
Destination Remote Network (5.3.1.2)
ARP (5.3.2)
Introduction to ARP (5.3.2.1)
ARP Functions (5.3.2.2)
ARP Request (5.3.2.3)
ARP Reply (5.3.2.4)
ARP Role in Remote Communication (5.3.2.5)
Removing Entries from an ARP Table (5.3.2.6)
ARP Tables (5.3.2.7)
ARP Issues (5.3.3)
ARP Broadcasts (5.3.3.1)
ARP Spoofing (5.3.3.2)
Summary (5.4)
Practice
Class Activities
Labs
 Packet Tracer Activities
Check Your Understanding Questions
Chapter 6 Network Layer
Objectives
Key Terms
Introduction (6.0)
Network Layer Protocols (6.1)
Network Layer in Communications (6.1.1)
The Network Layer (6.1.1.1)
Network Layer Protocols (6.1.1.2)
Characteristics of the IP Protocol (6.1.2)
Encapsulating IP (6.1.2.1)
Characteristics of IP (6.1.2.2)
IP – Connectionless (6.1.2.3)
IP – Best Effort Delivery (6.1.2.4)
IP – Media Independent (6.1.2.5)
IPv4 Packet (6.1.3)
IPv4 Packet Header (6.1.3.1)
IPv6 Packet (6.1.4)
Limitations of IPv4 (6.1.4.1)
Introducing IPv6 (6.1.4.2)
Encapsulating IPv6 (6.1.4.3)
IPv6 Packet Header (6.1.4.4)
Routing (6.2)
How a Host Routes (6.2.1)
Host Forwarding Decision (6.2.1.1)
Default Gateway (6.2.1.2)
Using the Default Gateway (6.2.1.3)
Host Routing Tables (6.2.1.4)
Router Routing Tables (6.2.2)
 Router Packet Forwarding Decision (6.2.2.1)
IPv4 Router Routing Table (6.2.2.2)
Directly Connected Routing Table Entries (6.2.2.4)
Remote Network Routing Table Entries (6.2.2.5)
Next-Hop Address (6.2.2.6)
Routers (6.3)
Anatomy of a Router (6.3.1)
A Router is a Computer (6.3.1.1)
Router CPU and OS (6.3.1.2)
Router Memory (6.3.1.3)
Inside a Router (6.3.1.4)
Connect to a Router (6.3.1.5)
LAN and WAN Interfaces (6.3.1.6)
Router Boot-up (6.3.2)
Bootset Files (6.3.2.1)
Router Bootup Process (6.3.2.2)
Show Version Output (6.3.2.4)
Configure a Cisco Router (6.4)
Configure Initial Settings (6.4.1)
Basic Switch Configuration Steps (6.4.1.1)
Basic Router Configuration Steps (6.4.1.2)
Configure Interfaces (6.4.2)
Configure Router Interfaces (6.4.2.1)
Verify Interface Configuration (6.4.2.2)
Configure the Default Gateway (6.4.3)
Default Gateway for a Host (6.4.3.1)
Default Gateway for a Switch (6.4.3.2)
Summary (6.5)
Practice
Class Activities
 Labs
Packet Tracer Activities
Check Your Understanding Questions
Chapter 7 IP Addressing
Objectives
Key Terms
Introduction (7.0)
IPv4 Network Addresses (7.1)
Binary and Decimal Conversion (7.1.1)
IPv4 Addresses (7.1.1.1)
Positional Notation (7.1.1.3)
Binary to Decimal Conversion (7.1.1.4)
Decimal to Binary Conversion (7.1.1.6)
Decimal to Binary Conversion Examples (7.1.1.7)
IPv4 Address Structure (7.1.2)
Network and Host Portions (7.1.2.1)
The Subnet Mask (7.1.2.2)
Logical AND (7.1.2.3)
The Prefix Length (7.1.2.5)
Network, Host, and Broadcast Addresses (7.1.2.6)
IPv4 Unicast, Broadcast, and Multicast (7.1.3)
Static IPv4 Address Assignment to a Host (7.1.3.1)
Dynamic IPv4 Address Assignment to a Host (7.1.3.2)
IPv4 Communication (7.1.3.3)
Unicast Transmission (7.1.3.4)
Broadcast Transmission (7.1.3.5)
Multicast Transmission (7.1.3.6)
Types of IPv4 Addresses (7.1.4)
Public and Private IPv4 Addresses (7.1.4.1)
Special User IPv4 Addresses (7.1.4.3)
 Legacy Classful Addressing (7.1.4.4)
Classless Addressing (7.1.4.6)
Assignment of IP Addresses (7.1.4.7)
IPv6 Network Addresses (7.2)
IPv4 Issues (7.2.1)
The Need for IPv6 (7.2.1.1)
IPv4 and IPv6 Coexistence (7.2.1.2)
IPv6 Addressing (7.2.2)
IPv6 Address Representation (7.2.2.1)
Rule 1 – Omit Leading 0s (7.2.2.2)
Rule 2 – Omit All 0 Segments (7.2.2.3)
Types of IPv6 Addresses (7.2.3)
IPv6 Address Types (7.2.3.1)
IPv6 Prefix Length (7.2.3.2)
IPv6 Unicast Addresses (7.2.3.3)
IPv6 Link-Local Unicast Addresses (7.2.3.4)
IPv6 Unicast Addresses (7.2.4)
Structure of an IPv6 Global Unicast Address (7.2.4.1)
Static Configuration of a Global Unicast Address (7.2.4.2)
Dynamic Configuration – SLAAC (7.2.4.3)
Dynamic Configuration – DHCPv6 (7.2.4.4)
EUI-64 Process and Randomly Generated (7.2.4.5)
Dynamic Link-Local Addresses (7.2.4.6)
Static Link-Local Addresses (7.2.4.7)
Verifying IPv6 Address Configuration (7.2.4.8)
IPv6 Multicast Addresses (7.2.5)
Assigned IPv6 Multicast Addresses (7.2.5.1)
Solicited-Node IPv6 Multicast Addresses (7.2.5.2)
Connectivity Verification (7.3)
ICMP (7.3.1)
 ICMPv4 and ICMPv6 (7.3.1.1)
ICMPv6 Router Solicitation and Router Advertisement Messages
(7.3.1.2)
Testing and Verification (7.3.2)
Ping – Testing the Local Stack (7.3.2.1)
Ping – Testing Connectivity to the Local LAN (7.3.2.2)
Ping – Testing Connectivity to Remote (7.3.2.3)
Traceroute – Testing the Path (7.3.2.4)
Summary (7.4)
Practice
Class Activities
Labs
Packet Tracer Activities
Check Your Understanding Questions
Chapter 8 Subnetting IP Networks
Objectives
Key Terms
Introduction (8.0)
Subnetting an IPv4 Network (8.1)
Network Segmentation (8.1.1)
Broadcast Domains (8.1.1.1)
Problems with Large Broadcast Domains (8.1.1.2)
Reasons for Subnetting (8.1.1.3)
Subnetting an IPv4 Network (8.1.2)
Octet Boundaries (8.1.2.1)
Subnetting on the Octet Boundary (8.1.2.2)
Classless Subnetting (8.1.2.3)
Classless Subnetting Example (8.1.2.6)
Creating 2 Subnets (8.1.2.7)
Subnetting Formulas (8.1.2.9)
 Creating 4 Subnets (8.1.2.10)
Subnetting a /16 and /8 Prefix (8.1.3)
Creating Subnets with a /16 prefix (8.1.3.1)
Creating 100 Subnets with a /16 Network (8.1.3.2)
Calculating the Hosts (8.1.3.3)
Creating 1000 Subnets with a /8 Network (8.1.3.5)
Subnetting to Meet Requirements (8.1.4)
Subnetting Based on Host Requirements (8.1.4.1)
Subnetting Based on Network Requirements (8.1.4.2)
Network Requirement Example (8.1.4.3)
Benefits of Variable Length Subnet Masking (8.1.5)
Traditional Subnetting Wastes Addresses (8.1.5.1)
Variable Length Subnet Masks (8.1.5.2)
Basic VLSM (8.1.5.3)
VLSM in Practice (8.1.5.5)
VLSM Chart (8.1.5.6)
Addressing Schemes (8.2)
Structured Design (8.2.1)
IPv4 Network Address Planning (8.2.1.1)
Planning to Address the Network (8.2.1.2)
Assigning Addresses to Devices (8.2.1.3)
Design Considerations for IPv6 (8.3)
Subnetting an IPv6 Network (8.3.1)
The IPv6 Global Unicast Address (8.3.1.1)
Subnetting Using the Subnet ID (8.3.1.2)
IPv6 Subnet Allocation (8.3.1.3)
Summary (8.4)
Practice
Class Activities
Labs
 Packet Tracer Activities
Check Your Understanding Questions
Chapter 9 Transport Layer
Objectives
Key Terms
Introduction (9.0)
Transport Layer Protocols (9.1)
Transportation of Data (9.1.1)
Role of the Transport Layer (9.1.1.1)
Transport Layer Responsibilities (9.1.1.2)
Conversation Multiplexing (9.1.1.3)
Transport Layer Reliability (9.1.1.4)
TCP (9.1.1.5)
UDP (9.1.1.6)
The Right Transport Layer Protocol for the Right Application
(9.1.1.7)
TCP and UDP Overview (9.1.2)
TCP Features (9.1.2.1)
TCP Header (9.1.2.2)
UDP Features (9.1.2.3)
UDP Header (9.1.2.4)
Multiple Separate Conversations (9.1.2.5)
Port Numbers (9.1.2.6)
Socket Pairs (9.1.2.7)
Port Number Groups (9.1.2.8)
The netstat Command (9.1.2.9)
TCP and UDP (9.2)
TCP Communication Process (9.2.1)
TCP Server Processes (9.2.1.1)
TCP Connection Establishment (9.2.1.2)
 TCP Session Termination (9.2.1.3)
TCP Three-way Handshake Analysis (9.2.1.4)
Reliability and Flow Control (9.2.2)
TCP Reliability – Ordered Delivery (9.2.2.1)
TCP Flow Control – Window Size and Acknowledgements
(9.2.2.4)
TCP Flow Control – Congestion Avoidance (9.2.2.5)
UDP Communication (9.2.3)
UDP Low Overhead versus Reliability (9.2.3.1)
UDP Datagram Reassembly (9.2.3.2)
UDP Server Processes and Requests (9.2.3.3)
UDP Client Processes (9.2.3.4)
TCP or UDP (9.2.4)
Applications that Use TCP (9.2.4.1)
Applications that Use UDP (9.2.4.2)
Summary (9.3)
Practice
Class Activities
Labs
Packet Tracer Activities
Check Your Understanding Questions
Chapter 10 Application Layer
Objectives
Key Terms
Introduction (10.0)
Application Layer Protocols (10.1)
Application, Presentation, and Session (10.1.1)
Application Layer (10.1.1.1)
Presentation and Session Layer (10.1.1.2)
TCP/IP Application Layer Protocols (10.1.1.3)
 How Application Protocols Interact with End-User Applications
(10.1.2)
Client-Server Model (10.1.2.1)
Peer-to-Peer Networks (10.1.2.2)
Peer-to-Peer Applications (10.1.2.3)
Common P2P Applications (10.1.2.4)
Well-Known Application Layer Protocols and
Services (10.2)
Web and Email Protocols (10.2.1)
Hypertext Transfer Protocol and Hypertext Markup Language
(10.2.1.1)
HTTP and HTTPS (10.2.1.2)
Email Protocols (10.2.1.3)
SMTP Operation (10.2.1.4)
POP Operation (10.2.1.5)
IMAP Operation (10.2.1.6)
IP Addressing Services (10.2.2)
Domain Name Service (10.2.2.1)
DNS Message Format (10.2.2.2)
DNS Hierarchy (10.2.2.3)
The nslookup Command (10.2.2.4)
Dynamic Host Configuration Protocol (10.2.2.5)
DHCP Operation (10.2.2.6)
File Sharing Services (10.2.3)
File Transfer Protocol (10.2.3.1)
Server Message Block (10.2.3.2)
Summary (10.3)
Practice
Class Activities
Labs
Packet Tracer Activities
Another random document with
no related content on Scribd:
Mouth-Frame.—In its broad outlines there is practically no variation
in this organ throughout the group, but in respect of the spines,
which are borne on the flanks of the jaws (mouth-papillae) and on
their apices (teeth and tooth-papillae) there is very great variation.
Teeth are always present. Mouth-papillae are very frequently
present, tooth-papillae are rarer, and it is only in a restricted number
of genera (Ophiocoma and its allies) that both mouth-papillae and
tooth-papillae are present at the same time.

Fig. 216.—A portion of an arm of Ophiohelus umbella, near the distal extremity,
treated with potash to show the skeleton, × 55. The vertebrae are seen to
consist of two curved rods united at their ends. The triangular side-plates
bear a row of movable hooks which articulate with basal outgrowths of the
plate. (After Lyman.)

Skeleton of the Disc.—This is typically composed of a mosaic of

plates of different sizes, but in some cases (Ophiomyxa, most
Streptophiurae, and Cladophiurae) these, with the exception of the
radials and genitals, are entirely absent, and the disc is then quite
soft and covered with a columnar epithelium, the persistent
ectoderm. Even the scuta buccalia may disappear. Radial shields
are absent in Ophiohelus. In many cases (Ophiothrix and
Ophiocoma) all the dorsal plates except the radials are concealed
from view by a covering of small spines. In some genera
(Ophiopyrgus) there are five large plates in the centre of the upper
part of the disc, which have been termed "calycinals" from a
mistaken comparison with the plates forming the cup or calyx of the
Pelmatozoa, but there is no connexion between the two sets of
structures.
The madreporite is usually quite rudimentary, but in Cladophiurae
there may be five madreporites, each with about 200 pores, and, of
course, five stone-canals.

The number of genital organs varies very much. In the small

Amphiura squamata there are two gonads, an ovary and a testis,
attached to each bursa, but in the larger species there may be very
many more.

We follow Bell's classification,[463] according to which the

Ophiuroidea are divided, according to the manner in which the
vertebrae move on one another (cf. Fig. 210), into three main orders,
since these movements are of prime importance in their lives.

(1) Streptophiurae, in which the faces of the vertebrae have

rudimentary knobs and corresponding depressions, so that the arms
can be coiled in the vertical plane. These are regarded as the most
primitive of Ophiuroidea.

(2) Zygophiurae, in which the vertebral faces have knobs and pits
which prevent their coiling in a vertical plane.

(3) Cladophiurae, in which the arms can be coiled as in (1) and are
in most cases forked. No teeth; the arm-spines are papillae, the
covering plates of the arms are reduced to granules.

Order I. Streptophiurae.
This is not a very well defined order; it includes a few genera
intermediate in character between the Cladophiurae and the
Zygophiurae, and believed to be the most primitive Ophiuroids living.
It is not divided into families. The vertebrae have rudimentary
articulating surfaces, there being two low bosses and corresponding
hollows on each side, and so they are capable of being moved in a
vertical plane, as in the Cladophiurae; the arms never branch, and
further, they always bear arm-spines and lateral arm-plates at least.
No species of this order are found on the British coast, but
Ophiomyxa pentagona, in which the dorsal part of the disc is
represented only by soft skin, is common in the Mediterranean.

Ophioteresis is devoid of ventral plates on the arms, and appears to

possess an open ambulacral groove, though this point has not been
tested in sections. Ophiohelus and Ophiogeron have vertebrae in
which traces of the double origin persist (see p. 491).

Order II. Zygophiurae.

This group includes all the common and better-known British forms.
They are divided into five families, all of which are represented in
British waters.

Fig. 217.—Aboral view of Ophioglypha (Ophiura) bullata. × 3. (From Wyville

Thomson.)
Fam. 1. Ophiolepididae.[464]—Arm inserted in a definite cleft in the
disc, or (expressing the same fact in another way) the interradial
lobes out of which the disc is composed are not completely united.
Radial shields and dorsal plates naked. Arm-spines smooth and
inserted on the posterior border of the lateral arm-plates.

Fig. 218.—Oral view of Ophioglypha (Ophiura) bullata. × 5. (From Wyville

Thomson.)

This family includes all the Brittle Stars of smooth porcelanous

aspect and provided with only short spines. Forbes[465] called them
Sand-stars, since their short spines render these animals incapable
of burrowing or of climbing well, and hence they appear to move
comparatively rapidly over firm ground, sand, gravel, or muddy sand,
and they are active enough to be able to capture small worms and
Crustacea. The prey is seized by coiling one of the arms around it.

One genus, Ophiura, is fairly common round the British coast, being
represented by O. ciliaris and O. albida; the former is the commoner.
An allied species dredged by H.M.S. "Challenger" is represented in
Figs. 217 and 218.

Ophiomusium (Fig. 219) is a very peculiar genus. The mouth-

papillae on each side of each mouth-angle are confluent, forming a
razor-like projection on each side of each mouth-angle (Fig. 220).
The arms are short, and the podia are only developed at the bases
of the arms. Ophiopyrgus has the dorsal surface raised into a conical
elevation protected by a central plate surrounded by five large
plates.

Fig. 219.—Aboral view of Ophiomusium pulchellum. × 7. (From Wyville

Thomson.)

In the remaining four families the arms are inserted on the under
surface of the disc; in other words, the interradial lobes which make
up the disc have completely coalesced dorsally; and the spines
stand out at right angles to the arm.

Fam. 2. Amphiuridae.—Mouth-papillae present, but no tooth-

papillae; radial shields naked; small scuta buccalia.

The most interesting Brittle Star belonging to this family is Amphiura

squamata (elegans), a small form, with a disc about ¼ inch in
diameter covered with naked plates. It is hermaphrodite and
viviparous, the young completing their development inside the
bursae of the mother. Occasionally the whole disc, with the
exception of the mouth-frame, is thrown off and regenerated. This
appears to be a device to enable the young to escape. Three other
species of Amphiura are found in British waters.

Fig. 220.—Oral view of Ophiomusium pulchellum. × 7. (From Wyville Thomson.)

Ophiactis is another genus belonging to this family, distinguished

from Amphiura by its shorter arms and smoother arm-spines. It lives
in the interstices of hard gravel. The British species, O. balli,
presents no special features of interest, but the Neapolitan O. virens
is an extraordinary form. It has six arms, three of which are usually
larger than the other three, for it is always undergoing a process of
transverse division, each half regenerating the missing part. It has
from 1 to 5 stone-canals, the number increasing with age; numerous
long-stalked Polian-vesicles in each interradius, and in addition a
number of long tubular canals which spring from the ring-canal, and
entwine themselves amongst the viscera.[466] All the canals of the
water-vascular system, except the stone-canals, contain non-
nucleated corpuscles, carrying haemoglobin,[467] the respiratory
value of which compensates for the loss of the genital bursae, which
have entirely disappeared.

Ophiopholis is distinguished from the foregoing genera by the

granular covering of its dorsal plates; whilst in Ophiacantha these
granules develop into prominent spinelets, and the arm-spines are
also thorny. Ophiopholis aculeata occurs in swarms in the branches
of the Firth of Clyde, and presents a most remarkable series of
variations in colour. Ophiopsila is a closely allied form, distinguished
by its large peristomial plates.

Fig. 221.—Oral view of Ophiacantha chelys. × 4. (From Wyville Thomson.)

Fam. 3. Ophiocomidae.—Both mouth-papillae and tooth-papillae

are present;[468] the arm-spines are smooth, and the disc is covered
with granules.

Ophiocoma nigra is the only common British representative of this

family. In this species the plates of the dorsal surface are completely
hidden from view by a covering of granules. Ophiarachna.

Fam. 4. Ophiothricidae.—Tooth-papillae alone present, mouth-

papillae absent; arm-spines roughened or thorny.

This family is represented only by Ophiothrix fragilis, which is

perhaps the most abundant of all British Ophiuroids, and has been
selected as the type for special description.

The back is covered with spinules, having, however, the triangular

radial plates bare. This produces a contrast-effect, which suggested
the name pentaphyllum, formerly used by some naturalists for the
species. It occurs in swarms, and presents variations in colour nearly
as marked as those of Ophiopholis. Ophiopteron is probably a
swimming Ophiuroid, as the lateral spines of each segment of the
arm are connected by a web of skin.

Order III. Cladophiurae.

Fig. 222.—Aboral view of young Astrophyton linckii, slightly enlarged. (From

Wyville Thomson.)

These, like the Streptophiurae, have the power of rolling the arms in
a vertical plane, but the articulating surfaces of the vertebrae are
well-developed and saddle-shaped. The dorsal surface of the disc
and arms is covered with a thick skin with minute calcifications.
Upper-arm plates wanting. Radial plates always present, though
occasionally represented by lines of scales. The order is divided into
three families, two of which are represented in British waters.

Fam. 1. Astroschemidae.—Arms unbranched. Astronyx is

comparatively common in the sea-lochs of Scotland. There are a
series of pad-like ridges on the arms, representing the side-plates
and bearing the spines. Astroschema.
Fam. 2. Trichasteridae.—Arms forked only at the distal ends.
Trichaster, Astrocnida.

Fam. 3. Euryalidae.—Arms forked to their bases. Gorgonocephalus

is occasionally taken in deep water off the north coast of Scotland. In
it the arms repeatedly fork, so that a regular crown of interlacing
arms is formed. The animal obviously clings to external objects with
these, for it is often taken in fishermen's nets with its arms coiled
around the meshes. The genital bursae are said to be represented
by slits which open directly into the coelom. (Lyman describes the
coelom as divided into ten compartments by radiating septa; it is
possible—even probable—that these are really the bursae.) An allied
species is common in the Bay of Fundy, being found in
comparatively shallow water. Astrophyton (Fig. 222) is closely allied
to Gorgonocephalus, differing only in trifling points. It is doubtful
whether the separation of these two genera is justified.

Fossil Ophiuroidea.—The Ophiuroidea are rather sparsely

represented among fossils, but in the Silurian and Devonian a series
of very interesting forms occur which are intermediate in character
between Starfish and Brittle Stars, and which were therefore in all
probability closely allied to the common ancestors of modern
Ophiuroids and Asteroids. Jaekel[469] has recently added largely to
our knowledge of these primitive forms, and has described a number
of new genera. Thus Eophiura from the Lower Silurian has an open
ambulacral groove, and the vertebrae are represented by an
alternating series of quadrate ossicles, each deeply grooved on its
under surface for the reception of the tentacle, which was not yet (as
in modern forms) enclosed in the vertebra. The lateral or
adambulacral plates extended horizontally outwards, and each bore
a series of spines at its outer edge.

A remarkable fact is that where the halves of the vertebrae (i.e. the
ambulacral ossicles) diverge in order to form the mouth-angles, no
less than five or six vertebrae are thus affected, instead of only two
as in modern forms. The actual "jaw," however, seems, as in modern
forms, to consist only of the first adambulacral fused to the second
ambulacral, so that instead of concluding with Jaekel that the "jaws"
of modern forms result from the fusion of five or six vertebrae, a
conclusion which would require that a number of tentacles had
disappeared, we may suppose that the gaping "angles" of these old
forms have, so to speak, healed up, except at their innermost
portions.

In Bohemura, which belongs to a somewhat younger stratum, the

structure is much the same, but the groove in the ambulacral ossicle
for the tentacle has become converted into a canal, and the
ambulacral groove itself has begun to be closed at the tip of the arm
by the meeting of the adambulacrals.

In Sympterura, a Devonian form described by Bather,[470] the two

ambulacral plates of each pair have thoroughly coalesced to form a
vertebra, but there is still an open ventral groove, and no ventral
plates.

In the Trias occurs the remarkable form Aspidura, which had short
triangular arms, in which the tentacle pores were enormous and the
ventral plates very small. The radial plates formed a continuous ring
round the edge of the disc. Geocoma from the Jurassic is a still more
typical Ophiuroid; it has long whip-like arms, and the dorsal skeleton
of the disc is made of fifteen plates, ten radials, and five interradials.
In the Jurassic the living genus Ophioglypha, appears.

The Cladophiurae are represented already in the Upper Silurian by

Eucladia, in which, however, the arms branch not dichotomously, as
they do in modern forms, but monopodially. There is a large single
madreporite.

Onychaster, with unbranched arms, which occurs in the

Carboniferous, is a representative of the Streptophiurae.
It will therefore be seen that the evolution of Ophiuroidea must have
begun in the Lower Silurian epoch. The Streptophiurae are a few
slightly modified survivors of the first Ophiuroids. By the time the
Devonian period had commenced, the division of the group into
Zygophiurae and Cladophiurae had been accomplished.

CHAPTER XVIII

ECHINODERMATA (CONTINUED): ECHINOIDEA = SEA-URCHINS

CLASS III. ECHINOIDEA

The Sea-urchins or Echinoidea (Gr. ἐχῖνος, Hedgehog or Sea-
urchin), which constitute the third class of the Eleutherozoa, have
derived both their popular and scientific names from the covering of
long spines with which they are provided. At first sight but little
resemblance is to be discerned between them and the Starfish and
Brittle Stars. They are devoid of any outgrowths that could be called
arms; their outline is generally either circular or that of an equilateral
pentagon, but as their height is almost always smaller than their
diameter, they are never quite spherical; sometimes it is so small
that the animals have the form of flattened discs.

All doubt as to the relationship of the Echinoidea to the Starfish is at

once dispelled in the mind of any one who sees one of the common
species alive. The surface is beset with delicate translucent tube-
feet, terminated by suckers resembling those of Starfish, although
capable of much more extension. The animal throws out these
organs, which attach themselves by their suckers to the substratum
and so pull the body along, whilst the spines are used to steady it
and prevent it from overturning under the unbalanced pull of the
tube-feet. When moving quickly the animal walks on its spines, the
tube-feet being little used. The tube-feet are distributed over five
bands, which run like meridians from one pole of the animal to the
other. These bands are termed "radii," and they extend from the
mouth, which is situated in the centre of the lower surface, up to the
neighbourhood of the aboral pole. The radii must be compared to the
ambulacral grooves on the oral surface of the arms of Starfish, and
hence in Urchins the aboral surfaces of the arms have, so to speak,
been absorbed into the disc, so that the oral surfaces have become
bent in the form of a semicircle. The radii are separated from one
another by meridional bands called "interradii," which correspond to
the interradial angles of the disc of a Starfish and to the sides of its
arms. The small area enclosed between the upper terminations of
the radii is called the "periproct," and this corresponds to the entire
dorsal surface of the Starfish, including that of the arms.

One of the commonest species of British Sea-urchin is Echinus

esculentus. In sheltered inlets, such as the Clyde, it is often left
exposed by the receding tide, whilst everywhere on the coast in
suitable localities it may be obtained by dredging at moderate depths
on suitable ground. In the Clyde it is easy to observe the habits of
the animal through the clear still water. It is then seen to frequent
chiefly rocky ground, and to exhibit a liking for hiding itself in
crevices. Often specimens will be seen clinging to the rock by some
of their tube-feet, and, as it were, pawing the under surface of the
water with the others. In the Clyde it feeds chiefly on the brown
fronds of Laminaria, with which the rocks are covered. In more
exposed situations, such as Plymouth Sound, it does not occur in
shallower water than 18 to 20 fathoms. At this depth it occurs on a
rocky ridge; but in 1899, after a south-west gale, all the specimens
had disappeared from this ridge, showing at what a depth wave
disturbance is felt.

A full-grown specimen is as large as a very large orange; its under

surface is flattened, and it tapers somewhat towards the aboral pole.
The outline is that of a pentagon with rounded angles. The spines in
Echinus esculentus are short in comparison to the diameter of the
body, and this is one of the characteristics of the species.
The animal is provided with a well-developed skeleton, consisting of
a mail of plates fitting closely edge to edge, and carrying the spines.
This cuirass bears the name "corona" (Fig. 227). It has two
openings, an upper and a lower, which are both covered with flexible
skin. The upper area is known as the "periproct" (Fig. 227, 2); it has
in it small isolated plates, and the anus, situated at the end of a small
papilla, projects from it on one side of the centre. The lower area of
flexible skin surrounds the mouth, and is called the "peristome" (Fig.
229), though it corresponds to considerably more than the peristome
of Asteroidea. In the mouth the tips of the five white chisel-like teeth
can be seen.

The plates forming the corona are, like all the elements of the
skeleton of Echinodermata, products of the connective tissue which
underlies the ectoderm, which in Echinoidea remains in a fully
developed condition covering the plates, and does not, as in
Ophiuroidea, dry up so as to form a mere cuticle. The ectoderm
consists of the same elements as that of Asteroidea, viz. delicate
tapering sense-cells with short sense-hairs, somewhat stouter
supporting cells and glandular cells. It is everywhere underlaid by a
plexus of nerve fibrils, which, in part, are to be regarded as the basal
outgrowths of the sense-cells and partly as the outgrowths of a
number of small bipolar ganglion-cells, found intermixed with the
fibres.

Fig. 223.—Aboral view of Echinus esculentus. × ½. (After Mortensen.)

Just as the muscular arm has been the determining factor in the
structure of the Ophiuroidea, so the movable spine has been the
leading factor in the evolution of Echinoidea. The spines have cup-
shaped basal ends, which are inserted on special projections of the
plates of the skeleton called tubercles. The tubercle is much larger
than the cup, and hence the spine has a great range of possible
motion. The spines differ from those of Starfish and Brittle Stars in
being connected with their tubercles by means of cylindrical sheaths
of muscle fibres, by the contraction of which they can be moved in
any direction. The muscles composing the sheath consist of an outer
translucent and an inner white layer. The former are easily
stimulated and soon relax; they cause the movements of the spines.
The latter require stronger stimulation, but when aroused respond
with a prolonged tetanus-like contraction, which causes the spines to
stand up stiffly in one position; these muscles can be torn across
sooner than forced to relax. Uexküll[471] has appropriately named
them "block musculature." These sheaths, like everything else, are
covered with ectoderm, which is, however, specially nervous, so that
we may say that the muscular ring is covered by a nerve-ring from
which stimuli are given off to the muscles.

The spines are, speaking generally, of two sizes, the larger being
known as "primary spines" and the smaller as "secondary." In many
Echinoidea these two varieties are very sharply contrasted, but in
Echinus esculentus there is not such a great difference in length,
and intermediate kinds occur. The forest of spines has an
undergrowth of pedicellariae. All Echinoidea possess pedicellariae,
which are much more highly developed than those of any Asteroid.
With few exceptions all the pedicellariae of Echinoidea possess
three jaws and a basal piece. This latter is, however, drawn out so as
to form a slender rod, which articulates with a minute boss on a plate
of the skeleton.

Of these pedicellariae there are in E. esculentus four varieties, viz.

(1) "tridactyle" (Fig. 225, C; Fig. 226, B): large conspicuous
pedicellariae with three pointed jaws, each armed with two rows of
teeth on the edges. There is a flexible stalk, the basal rod reaching
only half way up. These are scattered over the whole surface of the
animal.

(2) "Gemmiform" (Fig. 225, A, B; Fig. 226, A), so called from the
translucent, almost globular head. The appearance of the head is
due to the fact that there is on the outer surface of each jaw a sac-
like gland developed as a pouch of the ectoderm. From it are given
off two ducts which cross to the inner side of the blades and, uniting
into one, run in a groove to near the tip. The gland secretes a
poisonous fluid. The basal rod reaches up to the jaws, so that this
form of pedicellaria has a stiff stalk. On the inner side of each blade,
near the base, there is a slight elevation (Fig. 225, B, s), consisting
of cells bearing long cilia; this is a sense-organ for perceiving
mechanical stimuli. The gemmiform pedicellariae are particularly
abundant on the upper surface of the animal.

Fig. 224.—View of the apical region of Echinus esculentus, showing spines and
pedicellariae; drawn from the living specimen, × 3. a, Anus; g.p, genital
pore; i, interradius; mp, madreporite; per, periproct; p.gemm, gemmiform
pedicellaria; pod, podia; p.trid, tridactyle pedicellaria; p.trif, trifoliate
pedicellaria; r, radius; t.t, pore for terminal tentacle of the radial water-
vascular canal.
(3) "Trifoliate" (Fig. 225, E; Fig. 226, D): these are very small
pedicellariae, in which the jaws are shaped like leaves with the broad
end projecting outwards. They are scattered over the whole surface
of the body.

(4) "Ophicephalous" (Fig. 225, D; Fig. 226, C): pedicellariae in which

the jaws have broad rounded distal ends fringed with teeth; these
ends bear a resemblance to a snake's head, whence the name. The
bases are also broad and thin, with a strong median rib and a
peculiar semicircular hoop beneath the spot where they articulate
with one another. The three hoops of the three jaws work inside each
other in such a way as to cause the jaws to have a strong grip and to
be very difficult to dislocate from their mutual articulation.

The ophicephalous pedicellariae are in Echinus the most abundant

of all; and they alone extend on to the peristome, where a special
small variety of them is found.

A thorough investigation of the functions and reactions of the

pedicellariae has quite recently been made by von Uexküll.[472] He
showed, first of all, that there is a nervous centre in the stalk of each
pedicellaria (see below), which causes the organ to incline towards a
weak stimulus, but to bend away from a stronger stimulus. In the
head there is an independent nervous centre, which regulates the
opening and closing of the valves, and causes these to open on
slight stimulus and close when a stronger one is applied. The
amount of stimulus necessary to cause the pedicellariae to retreat
varies with the kind of pedicellariae, being least with the tridactyle
and most with the gemmiform, so that when a chemical stimulus,
such as a drop of dilute ammonia, is applied to the skin, the
tridactyle pedicellariae may be seen to flee from and the gemmiform
to approach the point of stimulation. In a living Sea-urchin, if the
attempt is made to seize the tridactyle pedicellariae they will evade
the forceps, but the ophiocephalous are easy to catch.
The tridactyle pedicellariae open with the very slightest mechanical
stimulus and close with rather greater mechanical stimuli or with
exceedingly slight chemical ones. Uexküll calls them "Snap-
pedicellariae," and their function is to seize and destroy the minute
swimming larvae of various sessile parasitic animals, which would
otherwise settle on the delicate exposed ectoderm of the Sea-urchin.

The gemmiform pedicellariae are brought into action when a more

serious danger threatens the Sea-urchin, such as an attack of a
Starfish. The corrosive chemical influence, which it can be proved
exudes not only from the stomach but even from the tube-feet of the
Starfish, causes the gemmiform pedicellariae to approach and open
widely. When the foe approaches so closely as to touch the sense-
organs (Fig. 225, B, s) situated on the inner side of the valves of
these pedicellariae, the blades close violently, wounding the
aggressor and causing its juice to exude, thus producing a renewed
and severe chemical stimulation which irritates the poison glands
and causes the poison to exude. The virulence of the poison may be
gauged from the fact that the bite of a single gemmiform pedicellaria
caused a frog's heart to stop beating.

Fig. 225.—The pedicellariae of Echinus acutus, drawn from a living specimen. A,

gemmiform pedicellaria, closed. B, gemmiform pedicellaria, open; g, poison
gland; s, sense-organ, × 3. C, tridactyle pedicellaria, × 6. D, ophicephalous
pedicellaria, × 9. E, trifoliate pedicellaria, × 12; a (in all figures), axial rod of
the stalk. (After Uexküll.)

Prouho[473] has described a combat between a Sea-urchin and a

Starfish. When the latter approached, the spines of the Sea-urchin
diverged widely (strong form of reaction to chemical stimulus),
exposing the gemmiform pedicellariae. These at once seized the
tube-feet of the enemy and the Starfish retreated, wrenching off the
heads of these pedicellariae; then the Starfish returned to the attack
and the same result followed, and this was repeated till all the
pedicellariae were wrenched off, when the Starfish enwrapped its
helpless victim with its stomach.

The minute trifoliate pedicellariae are brought into play by any

prolonged general irritation of the skin, such as bright light or a rain
of particles of grit or mud. They have the peculiarity that not all the
blades close at once, so that an object may be held by two blades
and smashed by the third. They may be seen in action if a shower of
powdered chalk is poured on the animal, when they seize the
particles and by breaking up any incipient lumps reduce the whole to
an impalpable powder, which the cilia covering the skin speedily
remove. In thus assisting in the removal of mechanical "dirt" they
earn the name which Uexküll has bestowed on them, of "cleaning
pedicellariae."

Fig. 226.—Views of a single blade of each kind of pedicellaria. A, blade of

gemmiform pedicellaria of Echinus elegans; g, groove for duct of poison
gland; B, blade of tridactyle pedicellaria of the same species; C, blade of
ophicephalous pedicellaria of the same species; r, ring for clamping this
blade to the other blades; D, blade of trifoliate pedicellaria of E. alexandri.
(After Mortensen.)

The ophicephalous pedicellariae, with their powerful bull-dog grip,

assist in holding small animals, such as Crustacea, till the tube-feet
can reach them and convey them to the mouth.

The number and variety of the pedicellariae, then, is an eloquent

testimony to the dangers to which the soft sensitive skins of the Sea-
urchin and other Echinodermata are exposed, and afford
confirmatory evidence in support of the view expressed above, that
the method adopted to defend the skin was one of the great
determining features which led to the division of the Asteroidea into
different races.

Fig. 227.—Dried shell of Echinus esculentus, showing the arrangement of the

plates of the corona. × 1. 1, The anus; 2, periproct, with irregular plates; 3,
the madreporite; 4, one of the other genital plates; 5, an ocular plate; 6, an
interambulacral plate; 7, an ambulacral plate; 8, pores for protrusion of the
tube-feet; 9, tubercles of the primary spines, i.e. primary tubercles.

The corona consists of five radial or "ambulacral" bands of plates

and five interradial, or as they are usually termed, "interambulacral"
bands of plates—ten in all. Each of the ten consists of two vertical
rows of plates throughout most of its extent, and each plate is
studded with large bosses, or "primary tubercles" for the primary
spines, smaller bosses called "secondary tubercles" for the
secondary spines, and finally, minute elevations called "miliary
tubercles" for the pedicellariae.
 Fig. 228.—The so-called calyx and the periproct of Echinus esculentus. × 4. 1,
Genital plates with genital pores; 2, ocular plates with pores for terminal
tentacles of the radial water-vascular canals; 3, madreporite; 4, periproct
with irregular plates; 5, anus. (After Chadwick.)

Even in the dried skeleton, however, the ambulacral plates can be

discriminated from the interambulacral by the presence of pores to
permit the passage of the tube-feet. These pores are arranged in
pairs, and each pair corresponds to a single tube-foot, since the
canal connecting the ampulla with the external portion of the tube-
foot is double in the Echinoidea. In Echinus esculentus there are
three pairs of such pores in each plate, in Strongylocentrotus
droëbachiensis four pairs. The ambulacral plate is really made up of
a series of "pore-plates," each carrying a single pair of pores, and
these become united in threes in Echinus and fours in
Strongylocentrotus, while in primitive forms like the Cidaridae they
remain separate. Each ambulacral and interambulacral area ends at
the edge of the periproct with a single plate. The plate terminating
the ambulacral band is pierced by a single pore for the exit of the
median tentacle, which, as in Asteroids, terminates the radial water-
vascular canal. Thus the aboral end of the radius in an Echinoid
corresponds to the tip of the arm in an Asteroid. The plate is termed
"ocular," because the terminal tentacle has a mass of pigmented
cells at its base; but no eye-cups can be seen, and there is no
evidence that this spot is specially sensitive to light. Species which
show special sensitiveness to light have often a large number of
what we may perhaps term secondary eyes. The plate terminating
the interambulacral series is termed the "genital plate," because it is
pierced by the duct of one of the five genital organs. One of the